Substituted pyridinones

Abstract

Disclosed are compounds of Formula I and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, and R5 are defined herein. These compounds are useful for treating diseases and conditions caused or exacerbated by unregulated p38 MAP Kinase and/or TNF activity. Pharmaceutical compositions containing the compounds, methods of preparing the compounds and methods of treatment using the compounds are also disclosed.

Description

FIELD OF THE INVENTION

The instant invention relates to substituted pyridinones that are useful for treating diseases and conditions caused or exacerbated by unregulated p38 MAP kinase activity. Pharmaceutical compositions containing the pyridinone compounds, methods of preparing the pyridone compounds and methods of treatment using the compounds are also disclosed.

BACKGROUND OF THE INVENTION

Numerous cell surface receptors use one or more of the mitogen-activated protein kinase (MAP kinase) cascades during signal transduction. MAP kinases are a family of protein-directed serine/threonine kinases that are activated by dual phosphorylation. One subgroup of the MAP kinases is p38 MAP kinase, which is activated by a variety of signals including proinflammatory cytokines such as tumor necrosis factor (TNF) and interleukin-1 (IL-1), as well as bacterial lipopolysaccharides and environmental stress such as osmotic shock and ultraviolet radiation (Ono, K. and J. Han, Cell Signal. 12: 1, 2000). Within the p38 kinase family, there are four distinct isozymes: p38 alpha, p38 beta, p38 gamma, and p38 delta. The p38 kinase family function downstream of an activating stimulus by phosphorylating and activating transcription factors (e.g. ATF2, CHOP and MEF2C) as well as other kinases (e.g. MAPKAP-2 and MAPKAP-3) (Trends in Cell biology 7, 353-361, 1997; Mol Cell Biology 19, 21-30, 1999; EMBO J 20, 466-479, 2001). Upon activation, the p38 kinase cascade leads to the induction of gene expression of several factors involved in inflammation and immunity including TNF, interleukin-6, granulocyte-macrophage colony stimulating factor (GM-CSF), and HIV long terminal repeat (Paul et al., Cell Signal. 9: 403-410, 1997). The products of the p38 phosphorylation stimulate the production of inflammatory cytokines and other proteins, including TNF and IL-1, and cyclooxygenase-2, and also possibly modulate the effects of these cytokines on their target cells, and thus stimulate inflammation processes (Lee, J. C. et al, Nature, 372: 376, 1994).

P38 MAP kinases have also been shown to promote apoptosis during ischemia in cardiac myocytes, which suggests that p38 MAP kinase inhibitors can be used to treat ischemic heart disease (J. Biol. Chem. 274, 6272, 1999). They are also required for T-cell HIV-1 replication and may be useful targets for AIDS therapy. P38 pathway inhibitors have been used to increase cancer cell sensitivity to cancer therapy also find use in the treatment of asthma (JPET 293, 281, 2000).

TNF is a cytokine and a potent proinflammatory mediator implicated in inflammatory conditions such as arthritis, asthma, septic shock, non-insulin dependent diabetes mellitus, multiple sclerosis, asthma, and inflammatory bowel disease. Thus inhibitors of p38 MAP kinases (required for TNF production) may be useful for the treatment of inflammatory conditions resulting from excessive cytokine production such as arthritis. (Boehm, J. C. and J. L. Adams, Exp. Opin. Ther. Patents 10: 25, 2000, and references cited therein). TNF has also been implicated in viral infections, such as HIV, influenza virus, and herpes virus including herpes simplex virus type-1 (HSV-1), herpes simplex virus type-2 (HSV-2), cytomegalovirus (CMV), varicella-zoster virus (VZV), Epstein-Barr virus, human herpesvirus-6 (HHV-6), human herpesvirus-7 (HHV-7), human herpesvirus-8 (HHV-8), pseudorabies and rhinotracheitis, among others.

Excessive or unregulated TNF production has also been shown to produce elevated levels of IL-1. Inhibition of TNF, therefore, should reduce levels of IL-1 (European Cytokine Netw 6, 225, 1995) and ameliorate disease states caused by unregulated IL-1 synthesis. Such disease states include rheumatoid arthritis, rheumatoid spondylitis, osteoarthritis, gouty arthritis, sepsis, septic shock, endotoxic shock, gram negative sepsis, toxic shock syndrome, adult respiratory distress syndrome, cerebral malaria, chronic pulmonary inflammatory disease, silicosis, pulmonary sarcosis, bone resorption diseases, reperfusion injury, graft versus host reaction, alallograft rejections, fever and myalgias due to infection, cachexia secondary to infection or malignancy, cachexia secondary to acquired immune deficiency syndrome (AIDS), AIDS related complex (ARC), keloid formation, scar tissue formation, Crohn's disease, ulcerative colitis, and pyresis.

IL-1 has also been shown to mediate a variety of biological activities such as the activation of T-helper cells, induction of fever, stimulation of prostaglandin or collagenase production, neutrophil chemotaxis, and the suppression of plasma iron levels (Rev. Infect. Disease, 6, 51 (1984)). Elevated levels of IL-1 have also been implicated in mediating or exacerbating a number of disease states including rheumatoid arthritis, osteoarthritis, rheumatoid spondylitis, gouty arthritis, inflammatory bowel disease, adult respiratory distress syndrome (ARDS), psoriasis, Crohn's disease, ulcerative colitis, anaphylaxis, muscle degeneration, cachexia, Reiter's syndrome, type I and type II diabetes, bone resorption diseases, ischemia reperfusion injury, arteriosclerosis, brain trauma, multiple sclerosis, sepsis, septic shock, and toxic shock syndrome. Viruses sensitive to TNF inhibition, such as HIV-1, HIV-2, HIV-3, are also affected by IL-1 production. In rheumatoid arthritis, both IL-1 and TNF induce collagenase synthesis and ultimately lead to tissue destruction within arthritic joints (Lymphokine Cytokine Res. (11): 253-256, (1992) and Clin. Exp. Immunol. 989:244-250, (1992)).

IL-6 is another pro-inflammatory cytokine, which is associated with many conditions including inflammation. Consequently, TNF, IL-1 and IL-6 affect a wide variety of cells and tissues and are important inflammatory mediators of a wide variety of disease states and conditions. The inhibition of these cytokines by inhibition or modulation of p38 kinase is of benefit in controlling, reducing and alleviating many of these disease states and conditions. Therefore, the present invention concerns finding small molecule inhibitors or modulators of p38 kinase and the p38 kinase pathway.

SUMMARY OF THE INVENTION

In a broad aspect, the invention provides compounds of Formula I (Embodiment I): or a pharmaceutically acceptable salt thereof, wherein

• R₁ is H, halogen, NO₂, alkyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkenyl, alkynyl, arylalkynyl, —CN, aryl, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, haloalkoxy, carboxyl, or arylalkanoyl,
  • wherein the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO₂R;
  • wherein the alkyl portion of the alkyl, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl groups is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkoxy, C₁-C₄ alkoxycarbonyl, or C₃-C₇ cycloalkyl;
• R₂ is H, OH, halogen, —OSO₂—(C₁-C₆)alkyl, —OSO₂-aryl, arylalkoxy, aryloxy, arylthio, arylthioalkoxy, arylalkynyl, alkoxy, aryloxy(C₁-C₆)alkyl, alkyl, alkynyl, —OC(O)NH(CH₂)_naryl, —OC(O)N(alkyl)(CH₂)_naryl, alkoxyalkoxy, dialkylamino, alkyl, alkoxy, aryl, arylalkyl, heteroaryl, heteroarylalkyl, arylalkenyl, heterocycloalkyl, heterocycloalkylalkyl, alkoxyalkoxy, NR₈R₉, dialkylamino, or CO₂R, wherein
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • each of which groups is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, —(C₁-C₄ alkyl)-NR₆C(O)NR₇—(C₁-C₆ alkoxy), —(C₁-C₄ alkyl)-NR₁₆C(O)NR₁₇—(C₃-C₆ cycloalkyl), —(C₁-C₄ alkyl)-NR₁₆C(O)NR₁₇—(C₃-C₆ cycloalkylalkyl), —(C₁-C₄ alkyl)-NR₁₆C(O)NR₁₇-(heteroaryl) wherein the heteroaryl group is optionally substituted with C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen or OH, haloalkyl, heteroaryl, heteroarylalkyl, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-NR₆(CO)NR₇—(C₁-C₆ alkoxy), —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, —(C₁-C₄alkyl)-NRC(O)NR₁₆R₁₇, haloalkoxy, alkyl, CN, hydroxyalkyl, dihydroxyalkyl, alkoxy, alkoxycarbonyl, phenyl, —SO₂-phenyl wherein the phenyl and —SO₂-phenyl groups are optionally substituted with 1, 2, or 3 groups that are independently halogen or NO₂, or —OC(O)NR₆R₇, wherein
  • R₁₆ and R₁₇ are independently H, C₁-C₆ alkyl, or C₁-C₆ alkoxy; or
  • R₁₆, R₁₇ and the nitrogen to which they are attached form a morpholinyl ring;
  • R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR₁₆R₁₇, alkanoyl, arylalkyl, arylalkoxy, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, alkoxycarbonyl, —SO₂-alkyl, —SO₂-aryl, OH, alkoxy, alkoxyalkyl, arylalkoxycarbonyl, —(C₁-C₄)alkyl-CO₂-alkyl, phenyl, heteroarylalkyl, heterocycloalkyloxy, alkenyl optionally substituted with —OC(O)NR₆R₇, aryl, heterocycloalkylalkanoyl, or arylalkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, alkoxy, heterocycloalkyl, heterocycloalkylalkyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy, or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, pyrrolidinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dionyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, alkoxycarbonyl, C₁-C₄ alkoxy, hydroxyl, hydroxyalkyl, dihydroxyalkyl, or halogen;
  • R at each occurrence is independently hydrogen or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
  • R₃₀ is C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
  • each R₈ is independently hydrogen, alkyl, alkanoyl, arylalkyl and arylalkanoyl, wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl;
  • each R₉ is hydrogen, alkyl, alkanoyl, arylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl, heteroaryl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, arylalkanoyl, —SO₂-phenyl, and aryl wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl;
• R₃ is H, halogen, alkoxycarbonyl, arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylalkoxy, —OC(O)N(alkyl)(CH₂)_naryl, aryloxy, arylthio, thioalkoxy, arylthioalkoxy, alkenyl, —NR₆R₇, NR₆R₇—(C₁-C₆)alkyl, or alkyl, wherein
  • the aryl portion of arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylalkoxy, —OC(O)N(alkyl)(CH₂)_naryl, and arylthioalkoxy, is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently, halogen, alkoxy, alkyl, haloalkyl, or haloalkoxy, wherein n is 0, 1, 2, 3, 4, 5, or 6; or
• R₄ is hydrogen or R₄ is alkyl unsubstituted or substituted with one or two groups that are independently CO₂R, OH, —CO₂—(C₁-C₆)alkyl, —C(O)NR₆R₇, —C(O)R₆, —N(R₃₀)C(O)NR₆R₇, —N(R₃₀)C(O)—(C₁-C₄ alkyl)-NR₆R₇, —OC(O)NR₆R₇, —OC(O)—(C₁-C₆ alkyl), —N(R₃₀)C(O)NR₁₆R₁₇, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, —N(R₃₀)C(O)—(C₁-C₄ alkyl)-NR₆R₇, or —NR₆R₇, —OC(O)NR₁₇-alkyl-heteroaryl, arylalkoxy, arylalkyl, heteroaryl, heteroarylalkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, R₆R₇N—(C₁-C₆ alkyl)-, —NR₆R₇, alkoxy, carboxaldehyde, —C(O)NR₆R₇, CO₂R, alkoxyalkyl, or alkoxyalkoxy, wherein the heteroaryl or aryl portions of is the above are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, —CO₂—(C₁-C₆)alkyl, —CONR₆R₇, —NR₆R₇, R₆R₇N—(C₁-C₆)alkyl-, nitro, haloalkyl, or haloalkoxy; and
• R₅ is H, or
• R₅ is aryl, arylalkyl, arylthioalkyl, alkyl optionally substituted with 1, 2, or 3 groups that are independently arylalkoxycarbonyl, —NR₈R₉, halogen, —C(O)NR₈R₉, alkoxycarbonyl, C₃-C₇ cycloalkyl, or alkanoyl, alkoxy, alkoxyalkyl optionally substituted with one trimethylsilyl group, amino, alkoxycarbonyl, hydroxyalkyl, dihydroxyalkyl, alkynyl, —SO₂-alkyl, alkoxy optionally substituted with one trimethylsilyl group, heterocycloalkylalkyl, cycloalkyl, cycloalkylalkyl, -alkyl-S-aryl, -alkyl-SO₂-aryl, heteroarylalkyl, heterocycloalkyl, -heteroaryl-heterocycloalkyl, heteroaryl, or alkenyl optionally substituted with one substituent selected from the group consisting of alkoxycarbonyl, -alkenyl-CO₂-alkyl, carboxyl, and —OC(O)NR₆R₇, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl optionally substituted with 1 or 2 groups that are independently NR₁₆R₁₇, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, —OC(O)NH₂, or —OC(O)NR₁₆R₁₇, OH, —OC(O)NR₁₆R₁₇, halogen, alkoxy wherein the alkyl group is optionally substituted with NR₁₆R₁₇, —C(O)NR₁₆R₁₇, OH or C₁-C₄ alkoxy, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO₂R, CN, OH, hydroxyalkyl, dihydroxyalkyl, —SO₂NR₁₆R₁₇, amidinooxime, —OC(O)NR₆R₇, —NR₆R₇, —NR₈R₉, R₆R₇N—(C₁-C₆ alkyl)-, carboxaldehyde, —S-alkyl wherein the alkyl group is optionally substituted with NR₁₆R₁₇, —C(O)NR₁₆R₁₇, OH or C₁-C₄ alkoxy, SO₂alkyl wherein the alkyl group is optionally substituted with NR₁₆R₁₇, —C(O)NR₁₆R₁₇, OH or C₁-C₄ alkoxy, —OC(O)—(C₁-C₆ alkyl), —SO₂H, —SO₂NR₆R₇, alkanoyl wherein the alkyl portion is optionally substituted with OH, halogen, —OC(O)—(C₁-C₆ alkyl), or alkoxy, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, heterocycloalkyl or heterocycloalkylalkyl, wherein the heterocycloalkyl group is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, tetrahydrofuranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR₁₆R₁₇, amidino, haloalkyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, —O—CH₂—O, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₆R_7, C₁-C₄ alkoxy, or OH, —O—CH₂CH₂—O—, or haloalkoxy; wherein
    • R₁₅ is H or C₁-C₆ alkyl; and
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

The invention also includes the intermediates that are useful in making the compounds of the invention.

These compounds bind and/or interact with p38 kinase and/or TNF. Preferably, they inhibit the activity of p38 kinase and/or TNF. They are therefore used in treating p38 map kinase or TNF mediated disorders. Preferably they are used in treating p38 alpha or TNF mediated disorders.

The instant invention also includes pharmaceutical compositions comprising at least one compound of formula I and at least one pharmaceutically acceptable carrier, solvent, adjuvant or excipient.

The instant invention also includes methods of treating a TNF mediated disorder, a p38 kinase mediated disorder, inflammation and/or arthritis in a subject, the method comprising treating a subject having or susceptible to such disorder or condition with a therapeutically-effective amount of a compound of Formula I.

DETAILED DESCRIPTION OF THE INVENTION

In a preferred aspect, the invention provides compounds of formula I wherein:

• when R₂ is benzyloxy, R₃ is H, R₄ is H, and R₅ is benzyl or methyl, R₁ is not hydrogen;
• no more than two of R₁, R₂, R₄, and R₅ are simultaneously hydrogen;
• R₆ and R₇ are not simultaneously OH;
• when R₂ is OH, R₄ is methyl and R₅ is phenyl, R₁ is not acetyl; and
• R₄ and R₅ are not simultaneously hydrogen.

Embodiment 2. Compounds of the formula: and the pharmaceutically acceptable salts thereof, wherein

• R₁ is H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkenyl, alkynyl, arylalkynyl, CN, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, carboxyl, or arylalkanoyl,
  • wherein the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO₂R;
  • wherein the alkyl portion of the alkyl, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl groups is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkoxy, C₁-C₄ alkoxycarbonyl, or cyclopropyl;
• R₂ is H, OH, halogen, —OSO₂—(C₁-C₆)alkyl, —OSO₂-aryl, arylalkoxy, aryloxy, arylthioalkoxy, arylalkynyl, alkoxy, phenyloxy(C₁-C₆)alkyl, —OC(O)NH(CH₂)_naryl, —OC(O)N(alkyl)(CH₂)_naryl, alkyl, alkynyl, alkoxyalkoxy, dialkylamino, heteroaryl, heterocycloalkyl, aryloxyalkyl, or CO₂R, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —NR₆R₇, haloalkyl, haloalkoxy, alkyl, heteroaryl, heteroarylalkyl, —(C₁-C₄)alkyl-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-NRC(O)NR₁₆R₁₇, CN, hydroxyalkyl, dihydroxyalkyl, —OC(O)NR₆R₇, or —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, wherein
    • R₁₆ and R₁₇ are independently H or C₁-C₆ alkyl; or
    • R₁₆, R₁₇ and the nitrogen to which they are attached form a morpholinyl ring;
    • R₆ and R₇ are independently at each occurrence H, alkyl, hydroxyalkyl, dihydroxyalkyl, alkoxy, alkoxyalkyl, alkanoyl, arylalkyl, arylalkoxy, arylalkoxycarbonyl, or arylalkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, alkoxy, heterocycloalkyl, heterocycloalkylalkyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy, or
    • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, alkoxycarbonyl, hydroxyl, hydroxyalkyl, dihydroxyalkyl, or halogen;
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • R at each occurrence is independently H or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
  • R₃₀ is C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
• R₄ is H, alkyl optionally substituted with one or two groups that are independently CO₂R, —CO₂alkyl, —C(O)NR₆R₇, —C(O)R₆, —N(R₃₀)C(O)NR₁₆R₁₇, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, arylalkoxy, heteroaryl, arylalkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, —NR₆R₇, —C(O)NR₆R₇, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the heteroaryl or aryl portions of the above are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, —CO₂—(C₁-C₆)alkyl, —CONR₆R₇, —NR₆R₇, R₆R₇N—(C₁-C₆)alkyl-, nitro, haloalkyl, or haloalkoxy; and
• R₅ is H, arylalkyl, alkyl optionally substituted with 1, 2, or 3 groups that are independently arylalkoxycarbonyl, —NR₈R₉, halogen, —C(O)NR₈R₉, alkoxycarbonyl, or alkanoyl, alkoxyalkyl optionally substituted with one trimethylsilyl group, alkoxycarbonyl, amino, hydroxyalkyl, dihydroxyalkyl, alkenyl optionally substituted with alkoxycarbonyl, alkynyl, —SO₂-alkyl, aryl, alkoxy optionally substituted with one trimethylsilyl group, heterocycloalkylalkyl, heteroarylalkyl, heterocycloalkyl, or heteroaryl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, arylalkoxy, hydroxyalkyl, dihydroxyalkyl, thioalkoxy, —SO₂alkyl, alkoxycarbonyl, arylalkoxycarbonyl, CO₂R, CN, OH, amidinooxime, NR₈R₉, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, hydroxyalkyl, dihydroxyalkyl, carboxaldehyde, —NR₆R₇, haloalkyl, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —(C₁-C₄ alkyl)-CO₂R, —(C₁-C₄ alkyl)-C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-CN, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, —O—CH₂—O—, —O—CH₂CH₂—O—, phenyl or haloalkoxy;
    • R₈ is hydrogen, alkyl, alkanoyl, arylalkyl and arylalkanoyl;
    • R₉ is alkyl, alkanoyl, arylalkyl, heteroaryl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, and arylalkanoyl.

Embodiment 3. Compounds according to embodiment 2 wherein

• R₁ is H, halogen, alkyl optionally substituted with C₁-C₄ alkoxycarbonyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, phenyl(C₁-C₆)alkoxy, phenyl(C₁-C₆)alkyl, CN, alkanoyl, alkoxy, C₂-C₄ alkynyl, C₂-C₆ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl, alkoxyalkyl, haloalkyl, or phenyl(C₁-C₆)alkanoyl,
  • wherein the phenyl groups are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, CF₃, OCF₃ or CO₂R;
  • wherein the alkyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy;
• R₂ is OH, phenyl(C₁-C₆)alkoxy, phenyloxy, phenyloxy(C₁-C₆)alkyl, phenyl(C₁-C₄) thioalkoxy, C₁-C₈ alkoxy, alkoxyalkoxy, —O—SO₂phenyl, alkynyl, phenyl(C₂-C₄) alkynyl, alkyl, —OC(O)NH(CH₂)_nphenyl, —OC(O)N(alkyl)(CH₂)_nphenyl, dialkylamino, pyridyl, pyrimidyl, pyridazyl, pyrazolyl, imidazolyl, pyrrolyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, tetrazolyl, pyrazinyl, benzimidazolyl, triazinyl, tetrahydrofuryl, piperidinyl, hexahydropyrimidinyl, thiazolyl, thienyl, or CO₂R, wherein
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, NR₆R₇, haloalkyl, haloalkoxy, hydroxyalkyl, dihydroxyalkyl, alkyl, phenyl, pyridyl, piperidinyl, piperazinyl, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, —(C₁-C₄ alkyl)-NRC(O)NR₁₆R₁₇, or —OC(O)NR₆R₇, wherein
    • R₆ and R₇ are independently at each occurrence H, alkyl, (C₁-C₄) hydroxyalkyl, (C₁-C₄)dihydroxyalkyl, (C₁-C₄)alkoxy, (C₁-C₄) alkoxy(C₁-C₄)alkyl, (C₁-C₄)alkanoyl, phenyl(C₁-C₄)alkyl, phenyl (C₁-C₄)alkoxy, phenyl(C₁-C₄)alkoxycarbonyl, or phenyl(C₁-C₄) alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, (C₁-C₄)alkoxy, (C₁-C₄)alkyl, CF₃, carboxaldehyde, NH₂, NH(C₁-C₆)alkyl, N(C₁-C₆)alkyl(C₁-C₆)alkyl, OCF₃; or
    • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkoxycarbonyl, or halogen; and
• R₄ is H, alkyl optionally substituted with one or two groups that are independently CO₂R, —CO₂alkyl, —C(O)NR₆R₇, —C(O)R₆, —N(R₃₀)C(O)NR₁₆R₁₇, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, —C(O)NR₆R₇, phenyl(C₁-C₆)alkoxy, phenyl(C₁-C₆)alkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the phenyl groups are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, CF₃, OCF₃;
• R₅ is phenyl(C₁-C₆)alkyl, (C₁-C₆)alkyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently phenyl C₁-C₄ alkoxycarbonyl, —NR₈R₉, halogen, —C(O)NR₈R₉, alkoxycarbonyl, or alkanoyl, phenyl, alkoxy, C₂-C₆ alkynyl, C₂-C₆ alkenyl optionally substituted with alkoxycarbonyl, indolyl, quinolinyl, isoquinolinyl, isoindolyl, dihydroindolyl, pyrazolyl, imidazolyl, dihydroisoindolyl, indolon-2-yl, indazolyl, benzimidazolyl, pyridyl, imidazolidine dione, pyrazolyl(C₁-C₆ alkyl), imidazolyl(C₁-C₆ alkyl), piperidinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, tetrahydroisoquinolinyl(C₁-C₆)alkyl, 1H-indazolyl(C₁-C₆)alkyl, dihydroindolon-2-yl(C₁-C₆ alkyl), indolinyl(C₁-C₆ alkyl), dihydrobenzimidazolyl(C₁-C₆ alkyl), or dihydrobenzoimidazolonyl(C₁-C₆ alkyl), pyridyl(C₁-C₆)alkyl, pyridazinyl(C₁-C₆)alkyl, pyrimidinyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, tetrahydrofuryl(C₁-C₆)alkyl, naphthyl(C₁-C₆)alkyl, morpholinyl(C₁-C₆)alkyl, tetrahydrofuryl(C₁-C₆)alkyl, thienyl(C₁-C₆)alkyl, piperazinyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, isoindolyl(C₁-C₆)alkyl, dihydroindolyl(C₁-C₆)alkyl, pyrazolyl(C₁-C₄)alkyl, imidazolyl(C₁-C₄)alkyl, dihydroisoindolyl(C₁-C₆)alkyl, indoon-2-yl(C₁-C₆)alkyl, indolon-2-yl(C₁-C₆) alkyl, or morpholinyl C₁-C₆ alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, halogen, C₁-C₆ alkoxy, phenyl C₁-C₆ alkoxy, C₁-C₆ thioalkoxy, C₁-C₆ alkoxycarbonyl, CO₂R, CN, —SO₂(C₁-C₆)alkyl, amidinooxime, NR₈R₉, —NR₆R₇, NR₆R₇ C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, amidino, C₁-C₄ haloalkyl, hydroxy C₁-C₆ alkyl, C₁-C₆ dihydroxyalkyl, or C₁-C₄ haloalkoxy; wherein
    • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl and phenyl C₁-C₆ alkanoyl; and
    • R₉ is aminoalkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl, indazolyl, and phenyl C₁-C₆ alkanoyl.

Embodiment 4. Compounds according to embodiment 3, wherein

• R₁ is H, halogen, C₁-C₄ alkyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, phenyl(C₁-C₄)thioalkoxy, or pyridyl; wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, (C₁-C₄)haloalkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-NRC(O)NR₁₆R₁₇, (C₁-C₄)haloalkoxy, hydroxyalkyl, C₁-C₆ dihydroxyalkyl, (C₁-C₆)alkyl, pyridyl, or R₆R₇N—(C₁-C₆ alkyl)-.

Embodiment 4a. Compounds according to embodiment 4, wherein R₁ is H.

Embodiment 4b. Compounds according to embodiment 4, wherein R₁ is halogen.

Embodiment 4c. Compounds according to embodiment 4, wherein R₁ is C₁-C₄ alkyl optionally substituted with C₁-C₄ alkoxycarbonyl.

Embodiment 5. Compounds according to embodiment 4, wherein

• R₅ is indolyl, pyridyl, pyridazinyl, pyrimidinyl, indazolyl, tetrahydroquinolyl, tetrahydroisoquinolyl, pyrazolyl, imidazolyl, furanyl, quinolinyl, isoquinolinyl, isoindolyl, dihydroindolyl, dihydroisoindolyl, indolon-2-yl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, 4 or 5 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, dihydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, —NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, —NR₈R₉, NR₆R₇—(C₁-C₄ alkyl), —C(O)NR₆R₇, or amidinooxime; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, phenyl C₁-C₄ alkyl, phenyl C₁-C₄ alkoxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen.

Embodiment 6. Compounds according to embodiment 5, wherein

• R₅ is indolyl, pyridyl, pyrimidinyl, pyrazolyl, furanyl, indazolyl, dihydroindolyl, dihydroisoindolyl, indolon-2-yl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, or 4 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, —C(O)NR₆R₇, —NR₈R₉, —(C₁-C₄)alkyl-C(O)NR₆R₇, —NR₆R₇, NR₆R₇—(C₁-C₄ alkyl)-, and amidinooxime.

Embodiment 7. Compounds according to embodiment 6, wherein

• R₅ is indolyl, pyridyl, pyrimidinyl, dihydroindolyl, dihydroisoindolyl, pyrazolyl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, or 4 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, —C(O)NR₆R₇, NR₈R₉, —(C₁-C₄)alkyl-C(O)NR₆R₇, —NR₆R₇, NR₆R₇—(C₁-C₄ alkyl)-, or amidinooxime; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkanoyl, C₁-C₄ alkoxy C₁-C₄ alkyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 8. Compounds according to embodiment 7, wherein

• R₅ is indolyl, pyridyl, pyrimidinyl, dihydroindolyl, dihydroisoindolyl, pyrazolyl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkoxy, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, NR₈R₉, —NR₆R₇, or NR₆R₇—(C₁-C₄ alkyl)-; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkanoyl, or C₁-C₄ alkoxy, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C —C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 9. Compounds according to embodiment 4, wherein

• R₅ is phenyl, phenyl(C₁-C₆)alkyl, or (C₁-C₆)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, benzyloxy, hydroxyalkyl, dihydroxyalkyl, thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂R, CN, amidinooxime, —NR₈R₉, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, amidino, CF₃, or OCF₃;
  • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl and phenyl C₁-C₆ alkanoyl; and
  • R₉ is aminoalkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, indazolyl, and phenyl C₁-C₄ alkanoyl.

Embodiment 10. Compounds according to embodiment 4, wherein

• R₅ is phenyl, phenyl(C₁-C₆)alkyl, which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, benzyloxy, thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂R, CN, amidinooxime, —NR₈R₉, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, R₆R₇NC(O)—(C₁-C₄ alkyl)-, R₆R₇NC(O)—(C₅-C₆ alkyl)-, —C(O)NR₆R₇, amidino, CF₃, or OCF₃; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, phenyl C₁-C₄ alkyl, phenyl C₁-C₄ alkoxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen;
  • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl and phenyl C₁-C₆ alkanoyl; and
  • R₉ is aminoalkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, indazolyl, and phenyl C₁-C₄ alkanoyl.

Embodiment 11. Compounds according to embodiment 10, wherein

• R₅ is phenyl, benzyl or phenethyl, wherein each is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, —NR₆R₇, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₈R₉, halogen, C₁-C₆ alkoxy, CO₂R, —(C₁-C₄ alkyl)-CO₂R, C₁-C₆ thioalkoxy, amidinooxime, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-C₁-C₆ alkoxycarbonyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, —(C₁-C₄ alkyl)-CN, CN, phenyl C₁-C₆ alkoxy, OH, C₁-C₄ haloalkyl, C₁-C₄ haloalkoxy, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, amidinooxime, —SO₂(C₁-C₆ alkyl), —O—CH₂—O—, —O—CH₂CH₂—O—, phenyl C₁-C₄ alkoxy, or phenyl; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkanoyl, or C₁-C₄ alkoxy, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃.

Embodiment 12. Compounds according to embodiment 11, wherein

• R₅ is phenyl, benzyl or phenethyl, each of which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently CN, halogen, C₁-C₄ alkoxy, CF₃, OCF₃, C₁-C₄ alkyl, —NR₈R₉, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₄ alkanoyl, or C₁-C₄ alkoxy, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 13. Compounds according to embodiment 4, wherein the R₅ group is of the formula: wherein

• Z₁ and Z₂ are independently H, halogen, C₁-C₄ alkyl, or CO₂R; and
• Z is —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —NR₈R₉, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkyl, CO₂R, or halogen; wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, or —SO₂(C₁-C₆ alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl, thiomorpholinyl, ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen; and
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

Embodiment 14. Compounds according to embodiment 4, wherein

• R₅ is pyrazolyl(C₁-C₆ alkyl), imidazolyl(C₁-C₆ alkyl), thienyl(C₁-C₆ alkyl), furanyl(C₁-C₆ alkyl), piperidinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, piperazinyl(C₁-C₆)alkyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, pyridazyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, tetrahydroisoquinolinyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, 1H-indazolyl(C₁-C₆)alkyl, dihydroindolyl(C₁-C₆ alkyl), dihydroindolon-2-yl(C₁-C₆ alkyl), indolinyl(C₁-C₆ alkyl), dihydroisoindolyl(C₁-C₆ alkyl), dihydrobenzimdazolyl(C₁-C₆ alkyl), or dihydrobenzoimidazolonyl(C₁-C₆ alkyl), wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently (C₁-C₆)alkyl, halogen, (C₁-C₆)alkoxy, (C₁-C₆)hydroxyalkyl, C₁-C₆ dihydroxyalkyl, phenyl(C₁-C₆)alkoxy, (C₁-C₆)thioalkoxy, (C₁-C₆)alkoxycarbonyl, phenyl(C₁-C₆)alkoxycarbonyl, OH, CO₂R, CN, amidinooxime, —NR₈R₉, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, amidino, piperazinyl, morpholinyl, —SO₂ (C₁-C₆) alkyl, —SO₂NH₂, —SO₂NH(C₁-C₆)alkyl, —SO₂N(C₁-C₆)alkyl(C₁-C₆)alkyl, (C₁-C₄)haloalkyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, —O—CH₂—O, —O—CH₂CH₂—O—, or (C₁-C₄)haloalkoxy; wherein
    • R₆ and R₇ are independently at each occurrence H, (C₁-C₆)alkyl, (C₁-C₆)alkoxy, (C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₁-C₆)alkoxycarbonyl, (C₁-C₆)hydroxyalkyl, C₁-C₆ dihydroxyalkyl, —(C₁-C₄)alkyl-CO₂—(C₁-C₆)alkyl, (C₁-C₆)alkanoyl, phenyl(C₁-C₆)alkyl, phenyl(C₁-C₆)alkoxy, or phenyl(C₁-C₆)alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, (C₁-C₄)alkoxy, OH, SH, C₃-C₆ cycloalkyl, NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), (C₁-C₄)alkyl, CF₃ or OCF₃; or
    • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen; and
    • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that Rr and R₇ are not simultaneously OH; and R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment 15. Compounds according to embodiment 14, wherein

• R₅ is pyrazolyl(C₁-C₆ alkyl), imidazolyl(C₁-C₆ alkyl), benzimidazolyl(C₁-C₆ alkyl), thienyl(C₁-C₆ alkyl), pyrimidyl(C₁-C₆)alkyl, indolyl(C₁-C₆ alkyl), dihydroindolyl(C₁-C₆ alkyl), dihydroisoindolyl(C₁-C₆ alkyl), dihydroindolon-2-yl(C₁-C₆ alkyl), pyridinyl(C₁-C₆ alkyl), piperazinyl(C₁-C₆ alkyl), or pyrazinyl(C₁-C₆ alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, C₁-C₆ alkoxycarbonyl, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, haloalkyl, C₁-C₆ alkanoyl,
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen.

Embodiment 16. Compounds according to embodiment 15, wherein

• R₅ is of the formula: wherein
• Z₅ is C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, C₁-C₆ alkoxycarbonyl, R₆R₇N—(C₁-C₆ alkyl)-, —NR₆R₇, CF₃, or C₁-C₆ alkanoyl, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen.

Embodiment 17. Compounds according to embodiment 15, wherein

• R₅ is of the formula: wherein
• Z₅ is C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, C₁-C₆ alkoxycarbonyl, R₆R₇N—(C₁-C₆ alkyl)-, —NR₆R₇, CF₃, or C₁-C₆ alkanoyl, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen.

Embodiment 18. Compounds according to either embodiment 16 or 17, wherein

• Z₅ is C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, halogen, C₁-C₆ alkoxycarbonyl, CF₃, or C₁-C₆ alkanoyl.

Embodiment 19. Compounds according to either embodiment 16 or 17, wherein

• Z₅ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —NR₆R₇, CF₃, or C₁-C₄ alkanoyl, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen.

Embodiment 20. Compounds according to embodiment 19, wherein

• Z₅ is —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkoxycarbonyl, halogen, cyclopropyl, OH, SH, or C₁-C₄ alkoxy.

Embodiment 21. Compounds according to embodiment 15, wherein

• • R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, haloalkyl, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 22. Compounds according to embodiment 15, wherein

• R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 23. Compounds according to embodiment 15, wherein

• • R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, haloalkyl, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 24. Compounds according to embodiment 15, wherein

• • R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 25. Compounds according to embodiment 15, wherein

• • R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, haloalkyl, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 26. Compounds according to embodiment 15, wherein

• R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 27. Compounds according to embodiment 15, wherein

• • R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, haloalkyl, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 28. Compounds according to embodiment 15, wherein

• • R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
• R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 29. Compounds according to embodiment 4, wherein

• R₅ is phenyl, which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, OH, C₁-C₆ alkoxycarbonyl, CF₃, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈; wherein
  • R₁₅ is H or C₁-C₆ alkyl;
  • R₁₆ and R₁₇ are independently H or C₁-C₆ alkyl; or
  • R₁₆, R₁₇, and the nitrogen to which they are attached form a morpholinyl ring; and
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

Embodiment 30. Compounds according to embodiment 29, wherein

• R₅ is of the formula:
• Z₁ is H, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, or C₁-C₄ alkoxy; and
• Z₂ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, OH, C₁-C₆ alkoxycarbonyl, or C₁-C₄ haloalkyl;
• Z₃ is H, C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, OH, C₁-C₆ alkoxycarbonyl, or C₁-C₄ haloalkyl; and wherein
• R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or C₁-C₆ alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

In this embodiment, it is preferred that at least one of Z₁, Z₂, and Z₃ is not hydrogen.

Embodiment 31. Compounds according to embodiment 30, wherein

• R₅ is of the formula: wherein
• Z₁ is H, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, or C₁-C₄ alkoxy; and
• Z₂ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, OH, C₁-C₆ alkoxycarbonyl, or C₁-C₄ haloalkyl;
• Z₃ is H, C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, OH, C₁-C₆ alkoxycarbonyl, or C₁-C₄ haloalkyl, and wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or C₁-C₆ alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

In this embodiment, it is preferred that at least one of Z₁, Z₂, and Z₃ is not hydrogen.

Embodiment 32. Compounds according to embodiment 30, wherein

• R₅ is of the formula: wherein
• Z₁ is H, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, or C₁-C₄ alkoxy; and
• Z₂ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, OH, C₁-C₆ alkoxycarbonyl, or C₁-C₄ haloalkyl;
• Z₃ is H, C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, OH, C₁-C₆ alkoxycarbonyl, or C₁-C₄ haloalkyl, and wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or C₁-C₆ alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

In this embodiment, it is preferred that at least one of Z₁, Z₂, and Z₃ is not hydrogen.

Embodiment 33. Compounds according to embodiment 29, wherein

• R₅ is either wherein
• Z₁ is H, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, or C₁-C₄ alkoxy; and
• Z₂ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, or —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈;
• Z₃ is H, C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, or —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈;
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy;
  • R₁₅ is H or C₁-C₆ alkyl;
  • R₁₆ and R₁₇ are independently H or C₁-C₆ alkyl; or
  • R₁₆, R₁₇, and the nitrogen to which they are attached form a morpholinyl ring; and
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that at least one of Z₁, Z₂, and Z₃ is not hydrogen.

Embodiment 34. Compounds according to embodiment 33, wherein

• R₅ is of the formula:
• Z₁ is H, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, or C₁-C₄ alkoxy; and
• Z₂ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, or —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈;
• Z₃ is H, C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄alkyl)-C(O)NR₆R_7, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, or —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈;
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy;
  • R₁₅ is H or C₁-C₆ alkyl;
  • R₁₆ and R₁₇ are independently H or C₁-C₆ alkyl; or
  • R₁₆, R₁₇, and the nitrogen to which they are attached form a morpholinyl ring; and
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that at least one of Z₁, Z₂, and Z₃ is not hydrogen.

Embodiment 35. Compounds according to embodiment 33, wherein

• R₅ is of the formula: wherein
• Z₁ is H, halogen, C₁-C₄ alkyl C₁-C₄ haloalkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, or C₁-C₄ alkoxy; and
• Z₂ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, or —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈;
• Z₃ is H, C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, or —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈;
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring, each of which is optionally substituted with 1 or 2 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy;
  • R₁₅ is H or C₁-C₆ alkyl;
  • R₁₆ and R₁₇ are independently H or C₁-C₆ alkyl; or
  • R₁₆, R₁₇, and the nitrogen to which they are attached form a morpholinyl ring; and
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that at least one of Z₁, Z₂, and Z₃ is not hydrogen.

Embodiment 36. A compound of the formula or a pharmaceutically acceptable salt thereof, wherein

• L and M are indepedently selected from —O—, —CH₂—, —S—, —NR—, —N(R)—N(R)—, C(═O)—, —SO₂—;
• R₅ is wherein
• X₁, X₂, X_a, X_b, X_c, X_d, and X_e at are independently selected from —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, H, OH, halogen, haloalkyl, alkyl, haloalkoxy, heteroaryl, heterocycloalkyl, C₃-C₇ cycloalkyl, R₆R₇N—(C₁-C₆ alkyl)-, —CO₂—(C₁-C₆)alkyl, —N(R)C(O)NR₆R₇, —N(R)C(O)—(C₁-C₆)alkoxy, CO₂R—(C₁-C₆ alkyl)-, or —SO₂NR₆R₇; wherein the heteroaryl and heterocycloalkyl groups are optionally substituted with —NR₆R₇, —C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, C₁-C₆ alkyl, C₁-C₆ alkoxy, or halogen; or
• R₅ is heteroaryl or heteroarylalkyl, wherein the heteroaryl and heteroaryl groups are optionally substituted with 1, 2, 3, or 4 groups that are independently —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, H, OH, halogen, haloalkyl, alkyl, haloalkoxy, R₆R₇N—(C₁-C₆ alkyl)-, —CO₂—(C₁-C₆)alkyl, —N(R)C(O)NR₆R₇, or —N(R)C(O)—(C₁-C₆)alkoxy; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₆ thiohydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen;
  • R at each occurrence is independently H or C₁-C₆ alkyl; and
• Y, Y₁, Y₂, Y₃, and Y₄ are independently selected from H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, alkenyl, alkynyl, CN, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, and carboxyl.

Embodiment 37. Compounds according to embodiment 36 of the formula or a pharmaceutically acceptable salt thereof.

Embodiment 38. Compounds according to embodiment 37, wherein

• • R₅ is

Embodiment 39. Compounds according to embodiment 31, wherein

• Y₂, Y₄, and Y are independently halogen; and
• Y₁ and Y₃ are both hydrogen.

Embodiment 40. Compounds according to embodiment 39, wherein

• R₅ is
• X₁ and X₂ are independently H, methyl, NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, or —(C₁-C₄ alkyl)-morpholinyl; and
• X_a and X_e are independently halogen, NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), methyl, or hydrogen.

In this embodiment, it is preferred that one of X_a and X_e is not hydrogen.

Embodiment 41. Compounds according to embodiment 40, wherein

• one of X_b and X_e is hydrogen and the other is —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —SO₂NR₆R₇, or halogen; where
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen.

Embodiment 42. Compounds according to embodiment 41, wherein

• R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃.

Embodiment 43. Compounds according to embodiment 42, wherein

• X_a is hydrogen, methyl, fluorine, or chlorine;
• X_c and X_d are both hydrogen;
• X_b is —NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇; wherein
• R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, or C₁-C₆ alkanoyl, wherein each of the above is optionally substituted with 1, 2, or 3 groups that are independently OH, SH, halogen, or C₃-C₆ cycloalkyl.

Embodiment 44. Compounds according to embodiment 39, wherein

• R₅ is
• X_a is H, fluoro, chloro, or methyl;
• X_e is hydrogen, halogen, or methyl; and
• X_b is H;
• X_d is H or halogen.

Embodiment 45. Compounds according to embodiment 44, wherein

• X_c is —SO₂NR₆R₇, or halogen; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen; or
• X_c is fluoro, chloro, —NH₂, —NH(C₁-C₆ alkyl), —N(C₁-C₆ alkyl)(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or piperazinyl, wherein the piperazinyl group is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen.

Embodiment 46. Compounds according to embodiment 44, wherein

• X_c is —C(O)NR₆R₇, —(C₁-C₆ alkyl)-C(O)NR₆R₇, —NR₆R₇, or R₆R₇N—(C₁-C₆ alkyl)-; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ dihydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, —NH₂, —NH(alkyl), —N(alkyl)(alkyl), —O-C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen.

Embodiment 47. Compounds according to embodiment 46, wherein

• R₆ is hydrogen; and
• R₇ is C₁-C₆ alkyl or C₁-C₆ alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), OH, SH, cyclopropyl, or C₁-C₄ alkoxy.

Embodiment 48. Compounds according to embodiment 47, wherein

• X_c is —C(O)NR₆R₇.

Embodiment 49. Compounds according to embodiment 47, wherein

• X_c is NR₆R₇, or R₆R₇N—(C₁-C₆ alkyl)-.

Embodiment 50. Compounds according to embodiment 38, wherein

• X_c is hydrogen;
• two of X_b, X_c, and X_d are hydrogen and the other is —C(O)NR₆R₇, —(C₁-C₆ alkyl)-C(O)NR₆R₇, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)- or —CO₂—(C₁-C₆)alkyl; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen; and
• X_e is hydrogen, methyl, C₁-C₂ alkoxy, or halogen.

Embodiment 51. Compounds according to embodiment 50, wherein

• X_b is —C(O)NR₆R₇, —(C₁-C₆ alkyl)-C(O)NR₆R₇, —NR₆R₇, or R₆R₇N—(C₁-C₆ alkyl)- wherein
• R₆ is hydrogen or C₁-C₄ alkyl;
• R₇ is OH, C₁-C₆ alkyl or C₁-C₆ alkanoyl, wherein the alkyl and alkanoyl groups substituted with 1, 2, or 3 groups that are independently NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₃-C₆ cycloalkyl, OH, or C₁-C₄ alkoxy.

Embodiment 52. Compounds according to embodiment 38, wherein

• X_a is halogen or methyl;
• X_b is H, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, or —CO₂—(C₁-C₆)alkyl;
• X_c is —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, halogen, —CO₂—(C₁-C₆)alkyl, NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or piperazinyl, wherein the piperazinyl group is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, C₁-C₄ dihydroxyalkyl, or halogen;
• X_d is hydrogen;
• X_e is H, methyl, NH₂, NH(C₁-C₆ alkyl) or N(C₁-C₆ alkyl)(C₁-C₆ alkyl).

Embodiment 53. Compounds according to embodiment 38, wherein

• X₁, X₂, X_a, X_b, X_c, X_d, and X_e are independently selected from H, OH, halogen, CF₃, alkyl, OCF₃, pyridyl, pyridazinyl, pyrimidyl, pyrazinyl, thienyl, furyl, pyrrolyl, piperidinyl, piperazinyl, or C₃-C₇ cycloalkyl, wherein each of the above is optionally substituted with —NR₆R₇, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, C₁-C₆ alkyl, C₁-C₆ alkoxy, or halogen.

Embodiment 54. Compounds according to embodiment 37, wherein

• R₅ is a heteroaryl or heteroarylalkyl group, where each heteroaryl is pyrazolyl, imidazolyl, furanyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, pyrazolyl, imidazolyl, dihydroindolyl, dihydroisoindolyl, indolon-2-yl, quinolinyl, isoquinolinyl, tetrahydroisoquinolinyl, dihydroisoquinolinyl, or indolyl, each of which is optionally substituted with 1, 2, 3, or 4 groups that are independently —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, hydrogen, hydroxy, halogen, haloalkyl, alkyl, haloalkoxy, R₆R₇N—(C₁-C₆ alkyl)-, —CO₂—(C₁-C₆)alkyl, —N(R)C(O)NR₆R₇, or —N(R)C(O)—(C₁-C₆)alkoxy; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ thiohydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF.

Embodiment 55. Compounds according to embodiment 54, wherein

• Y₂, Y₄, and Y are independently halogen; and
• Y₁ and Y₃ are both hydrogen.

Embodiment 56. Compounds according to embodiment 55, wherein

• X₁ and X₂ are independently H, methyl, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, or —(C₁-C₄ alkyl)-morpholinyl.

Embodiment 57. Compounds according to embodiment 56, wherein

• R₅ is pyridyl C₁-C₆ alkyl, pyrimidinyl C₁-C₆ alkyl, or pyrazinyl C₁-C₆ alkyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇.

Embodiment 58. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
• Z₅ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 59. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
• Z₅ is hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-C(O)NR₆R₇, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 60. Compounds according to embodiment 57, wherein

• R₅ is of the formula:
  • Z₁₀ is H or methyl; and
  • Z₂₀ is —(C₁-C₄ alkyl)-C(O)NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 61. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
  • Z₁₀ is H or methyl; and
  • Z₂₀ is —(C₁-C₄ alkyl)-C(O)NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 62. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
  • Z₁₀ is H or methyl; and
  • Z₂₀ is —(C₁-C₄ alkyl)-C(O)NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 63. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
  • Z₁₀ is H or methyl; and
  • Z₂₀ is —(C₁-C₄ alkyl)-C(O)NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 64. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
  • Z₁₀ is H or methyl; and
  • Z₂₀ is —(C₁-C₄ alkyl)-C(O)NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 65. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
  • Z₁₀ is H or methyl; and
  • Z₂₀ is —(C₁-C₄ alkyl)-C(O)NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 66. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
  • Z₁₀ is H or methyl; and
  • Z₂₀ is —(C₁-C₄ alkyl)-C(O)NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 67. Compounds according to embodiment 57, wherein

• R₅ is of the formula: wherein
  • Z₁₀ is H or methyl; and
  • Z₂₀ is —(C₁-C₄ alkyl)-C(O)NR₆R₇, hydroxy(C₁-C₄)alkyl, C₁-C₄ dihydroxyalkyl, OH, halogen, CF₃, (C₁-C₄)alkyl, OCF₃, —NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment A7. Compounds according to embodiment 1 wherein

• R₁ is H, halogen, alkyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₆ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkynyl, C₁-C₄ haloalkyl, carboxaldehyde, C₁-C₄ hydroxyalkyl, phenyl(C₁-C₆)alkoxy, benzyl, phenethyl, phenpropyl, CN, or phenyl(C₁-C₆)alkanoyl,
  • wherein the phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, CF₃, OCF₃ or CO₂H;
• R₂ is OH, benzyloxy, phenyloxy, phenyloxy(C₁-C₆)alkyl, phenyl(C₁-C₄)thioalkoxy, —OC(O)NH(CH₂)_nphenyl, —OC(O)N(alkyl)(CH₂)_nphenyl, di(C₁-C₆)alkylamino, C₂-C₆ alkynyl, pyridyl, pyrimidyl, pyridazyl, pyrazolyl, imidazolyl, pyrrolyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, tetrazolyl, pyrazinyl, benzimidazolyl, triazinyl, tetrahydrofuryl, piperidinyl, hexahydropyrimidinyl, thiazolyl, thienyl, or CO₂H, wherein
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, or NR₆R₇—(C₁-C₆ alkyl)-,
• R₄ is H, alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenyl(C₁-C₆)alkoxy, phenyl(C₁-C₆)alkyl, hydroxyalkyl, wherein the phenyl groups are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, CF₃, or OCF₃; and
• R₅ is phenyl(C₁-C₆)alkyl, (C₁-C₆)alkyl, phenyl, piperidinyl(C₁-C₆)alkyl, thienyl(C₁-C₆) alkyl, indolyl, quinolinyl, isoquinolinyl, isoindolyl, indol-2-onyl, indazolyl, indolyl (C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, isoindolyl(C₁-C₆)alkyl, indol-2-onyl(C₁-C₆)alkyl, naphthyl(C₁-C₆)alkyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, or wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, benzyloxy, thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, CF₃, or OCF₃;
    • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl and phenyl C₁-C₆ alkanoyl; and
  • R₉ is aminoalkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, indazolyl, and phenyl C₁-C₄ alkanoyl.

In this embodiment, it is preferred that when R₂ is benzyloxy, R₄ is H, and R₅ is benzyl or methyl, R₁ is not hydrogen; and

• • no more than two of R₁, R₂, R₄, and R₅ are simultaneously hydrogen.

Embodiment A8. Compounds according to embodiment A7 wherein

• R₁ is H, halogen, C₁-C₄ alkyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, phenyl(C₁-C₄)thioalkoxy, or pyridyl; wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C i-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, or NR₆R₇—(C₁-C₆ alkyl)-.

Embodiment A9. Compounds according to embodiment A7 wherein

• R₄ is H, (C₁-C₆)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenyl(C₁-C₆)alkoxy, or hydroxy(C₁-C₆)alkyl, wherein
  • the phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, C₁-C₄ alkoxy, C₁-C₄ alkyl, nitro, CF₃, OCF₃; and
• R₅ is benzyl, phenethyl, phenpropyl, phenbutyl, (C₁-C₆)alkyl, phenyl, pyridyl, pyrimidyl, indolyl, indazolyl, indolyl(C₁-C₆)alkyl, naphthyl(C₁-C₆)alkyl, thienyl(C₁-C₆)alkyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆)alkyl, and wherein
  • each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently alkyl, halogen, alkoxy, benzyloxy, thioalkoxy, —CO₂(C₁-C₅ alkyl), CF₃, OCF₃, CO₂H, CN, amidinooxime.

In this embodiment, it is preferred that when R₂ is benzyloxy, R₄ is H, and R₅ is benzyl or methyl, R₁ is not hydrogen; and

• • no more than two of R₁, R₂, R₄, and R₅ are simultaneously hydrogen.

Embodiment A10. Compounds according to embodiment A7, wherein

• R₄ is H, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenyl(C₁-C₆)alkoxy, benzyl, phenethyl, phenpropyl, or hydroxy(C₁-C₆)alkyl, wherein
  • the phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, C₁-C₄ alkoxy, C₁-C₄ alkyl, nitro, CF₃, OCF₃; and
• R₅ is indolyl, quinolinyl, isoquinolinyl, isoindolyl, indol-2-onyl, indolyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, isoindolyl(C₁-C₆)alkyl, indol-2-onyl(C₁-C₆)alkyl, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, —NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, or amidinooxime; wherein
  • R₆ and R₇ are independently at each occurrence H, alkyl, hydroxyalkyl, alkoxy, alkoxyalkyl, alkanoyl, phenylalkyl, phenylalkoxy, or phenylalkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, hydroxy, C₁-C₄ alkoxy, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
• R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A11. Compounds according to embodiment A7 wherein

• R₁ is chloro, bromo, iodo, or H; and
• R₅ is benzyl, phenethyl, phenpropyl, phenyl, quinolinyl, indolyl, isoquinolinyl, isoindolyl, indol-2-onyl, indolyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆) alkyl, isoindolyl(C₁-C₆)alkyl, indol-2-onyl(C₁-C₆)alkyl, piperidinyl C₁-C₄ alkyl, thienyl C₁-C₄ alkyl, —CH₂-pyridyl, or pyridyl, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, NR₈R₉, NR₆R₇ C₁-C₄ alkyl, —C(O)NR₆R₇, and amidinooxime; wherein
  • R₆ and R₇ are independently at each occurrence H, alkyl, hydroxyalkyl, alkoxy, alkoxyalkyl, alkanoyl, phenylalkyl, phenylalkoxy, or phenylalkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, hydroxy, C₁-C₄ alkoxy, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A12. Compounds according to embodiment A11, wherein

• R₅ is benzyl, phenethyl, phenpropyl, or phenyl, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, NR₈R₉, NR₆R₇ C₁-C₄ alkyl, —C(O)NR₆R₇, and amidinooxime.

Embodiment A13. Compounds according to embodiment A11, wherein

• R₅ is quinolinyl, indolyl, isoquinolinyl, isoindolyl, indol-2-onyl, indolyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, isoindolyl(C₁-C₆)alkyl, indol-2-onyl(C₁-C₆)alkyl, piperidinyl C₁-C₄ alkyl, thienyl C₁-C₄ alkyl, —CH₂-pyridyl, or pyridyl, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, NR₈R₉, NR₆R₇ C₁-C₄ alkyl, —C(O)NR₆R₇, and amidinooxime.

Embodiment A14. Compounds according to any one of embodiments A11, A12, or A13 wherein

• R₂ is benzyloxy, or phenethyloxy;
  • each of the above is unsubstituted or substituted with 1, 2, or 3, groups that are independently —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, fluoro, chloro, bromo, CF₃, or (C₁-C₄)alkyl.

Embodiment A15. Compounds according to any one of embodiments A11, A12 or A13 wherein

• R₂ is phenyloxy(C₁-C₆)alkyl, wherein the phenyl group is unsubstituted or substituted with 1, 2, or 3, groups that are independently —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, fluoro, chloro, bromo, CF₃, or (C₁-C₄)alkyl.

Embodiment A16. Compounds according to embodiment A1, wherein

• R₁ is H, halogen, C₁-C₄ alkyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkynyl, or carboxaldehyde.

Embodiment A17. Compounds according to embodiment A16, wherein

• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, or NR₆R₇—(C₁-C₆ alkyl)-.

Embodiment A18. Compounds according to embodiment A17, wherein

• R₄ is H, or (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, OH, or —NR₆R₇.

Embodiment A19. Compounds according to embodiment A18, wherein

• R₅ is phenyl, naphthyl, indolyl, pyridyl, quinolinyl, isoquinolinyl, isoindolyl, indol-2-onyl, indolyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, isoindolyl(C₁-C₆)alkyl, indol-2-onyl(C₁-C₆)alkyl, pyridazinyl, pyrimidinyl, or pyrazinyl, pyridazinyl(C₁-C₆)alkyl, pyrimidinyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆) alkyl, each of which is unsubstituted or substituted with 1, 2, 3, 4 or 5 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, —NR₈R₉, —C(O)NR₆R₇, NR₆R₇ C₁-C₄ alkyl, and amidinooxime; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, phenyl C₁-C₄ alkyl, phenyl C₁-C₄ alkoxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, hydroxy, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, C₃-C₆ cycloalkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A20. Compounds according to embodiment A19, wherein

• R₁ is H, halogen, methyl, ethyl, C₂-C₄ alkenyl C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, NR₆R₇ C₁-C₄ alkyl, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, or pyridyl; and
• R₄ is H, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, OH, or —NR₆R₇.

Embodiment A21. Compounds according to embodiment A20, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₆ alkyl, —NR₁₀R₁₁, C₁-C₄ alkoxy, —C(O)NR₁₀R₁₁, —CO₂H, NR₁₀R₁₁ C₁-C₄ alkyl, C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, C₁-C₆ alkoxy, CHO, —SO₂NH₂, C₁-C₄ haloalkyl, C₁-C₆ hydroxyalkyl, —C₁-C₄ alkyl-NR₁₂C(O)NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)OR₁₅, or —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-R₁₅, wherein
  • R₁₀ and R₁₁ at each occurrence are independently H, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, OH, —SO₂ (C₁-C₆ alkyl), or C₁-C₆ alkanoyl, or
  • R₁₀, R₁₁, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl or halogen,
  • R₁₂ is H or C₁-C₆ alkyl;
  • R₁₃ and R₁₄ are independently H or C₁-C₆ alkyl; or
  • R₁₃ and R₁₄ and the nitrogen to which they are attached form a morpholinyl ring; and
  • R₁₅ is C₁-C₆ alkoxy; —OC(O)C₁-C₆ alkyl, OH.

Embodiment A22. Compounds according to embodiment A21, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₆ alkyl, —NR₁₀R₁₁, NR₁₀R₁₁ C₁-C₆ alkyl, C₁-C₄ alkoxy, or —C(O)NR₁₀R₁₁, —CO₂H, —C₁-C₄ alkyl-NR₁₀R₁₁, C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, C₁-C₆ alkoxy, CHO, —SO₂NH₂, C₁-C₄ haloalkyl, C₁-C₆ hydroxyalkyl, —C₁-C₄ alkyl-NR₁₂C(O)NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)OR₁₅, or —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-R₁₅ wherein
  • R₁₀ and R₁₁ at each occurrence are independently H, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, OH, —SO₂ (C₁-C₆ alkyl), or C₁-C₆ alkanoyl,
  • R₁₂ is H or C₁-C₆ alkyl;
  • R₁₃ and R₁₄ are independently H or C₁-C₆ alkyl; or
  • R₁₃ and R₁₄ and the nitrogen to which they are attached form a morpholinyl ring; and
  • R₁₅ is C₁-C₆ alkoxy; —OC(O)C₁-C₆ alkyl, OH.

Embodiment A23. Compounds according to embodiment A22, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₆ alkyl, —NR₁₀R₁₁, NR₁₀R₁₁ C₁-C₄ alkyl, C₁-C₄ alkoxy, —C(O)NR₁₀R₁₁, wherein
  • R₁₀ and R₁₁ at each occurrence are independently H, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, OH, —SO₂ (C₁-C₆ alkyl), C₁-C₆ alkanoyl.

Embodiment A24. Compounds according to embodiment A23, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₆ alkyl, —NR₁₀R₁₁, or C₁-C₄ alkoxy.

Embodiment A25. Compounds according to embodiment A23, wherein

• R₅ is substituted with at least one —C(O)NR₁₀R₁₁.

Embodiment A26. Compounds according to embodiment A25, wherein

• R₁₀ and R₁₁ at each occurrence are independently H, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl.

Embodiment 27. Compounds according to embodiment A26, wherein

• R₁₀ is H.

Embodiment A28. Compounds according to embodiment A25, wherein

• R₁₀ and R₁₁ at each occurrence are independently H, C₁-C₆ alkyl, OH, —SO₂ (C₁-C₆ alkyl), C₁-C₆ alkanoyl.

Embodiment A29. Compounds according to embodiment A20, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₆ alkyl, NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, —C(O)NR₁₀R₁₁, wherein each of the above alkyl groups is optionally substituted with 1 or 2 groups that are independently OH, or methoxy; wherein
  • R₁₀, R₁₁, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl or halogen.

Embodiment A30. Compounds according to embodiment A20, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₆ alkyl, C₁-C₄ alkoxy, —CO₂H, —C₁-C₄ alkyl-NR₁₀R₁₁, C₁-C₆ alkoxycarbonyl, C₁-C₆ alkoxy, CHO, —SO₂NH₂, C₁-C₄ haloalkyl, C₁-C₆ hydroxyalkyl, —C₁-C₄ alkyl-NR₁₂C(O)NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)OR₁₅, or —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-R₁₅, —OC(O)C₁-C₆ alkyl, or OH wherein
  • R₁₂ is H or C₁-C₆ alkyl;
  • R₁₃ and R₁₄ are independently H or C₁-C₆ alkyl; or
  • R₁₃ and R₁₄ and the nitrogen to which they are attached form a morpholinyl ring;
  • R₁₅ is C₁-C₆ alkoxy.

Embodiment A31. Compounds according to embodiment A30, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, —CO₂H, C₁-C₄ alkoxycarbonyl, C₁-C₄ alkoxy, CHO, —SO₂NH₂, C₁-C₄ haloalkyl, C₁-C₄ hydroxyalkyl.

Embodiment A32. Compounds according to embodiment A30, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, —CO₂H, —C₁-C₄ alkyl-NR₁₀R₁₁, —C₁-C₄ alkyl-NR₁₂C(O)NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)OR₁₅, or —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-R₁₅, or —OC(O)C₁-C₆ alkyl, wherein
  • R₁₂ is H or C₁-C₆ alkyl;
  • R₁₃ and R₁₄ are independently H or C₁-C₆ alkyl; or
  • R₁₃ and R₁₄ and the nitrogen to which they are attached form a morpholinyl ring;
  • R₁₅ is C₁-C₆ alkoxy.

Embodiment A33. Compounds according to embodiment A31, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, —CO₂H, —C₁-C₄ alkyl-NR₁₀R₁₁, —C₁-C₄ alkyl-NR₁₂C(O)NR₁₃R₁₄, —C₁-C₄ alkyl-NR₁₂C(O)—(C₁-C₄ alkyl)-NR₁₃R₁₄, wherein
  • R₁₂ is H or C₁-C₆ alkyl;
  • R₁₃ and R₁₄ are independently H or C₁-C₆ alkyl; or
  • R₁₃ and R₁₄ and the nitrogen to which they are attached form a morpholinyl ring.

Embodiment A34. Compounds according to any one of embodiments A30, A31, A32, or A33, wherein the phenyl group is substituted with two groups that are meta to each other.

Embodiment A35. Compounds according to any one of embodiments A30, A31, A32, or A33, wherein the phenyl group is substituted with two groups that are para to each other.

Embodiment A36. Compounds according to embodiment A20, wherein

• R₅ is indolyl, pyridyl, pyridazinyl, pyrimidinyl, indazolyl, quinolinyl, isoquinolinyl, isoindolyl, indol-2-onyl, pyridazinyl, pyrimidinyl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, 4 or 5 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, NR₈R₉, NR₆R₇ C₁-C₄ alkyl, —C(O)NR₆R₇, or amidinooxime; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, phenyl C₁-C₄ alkyl, phenyl C₁-C₄ alkoxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A38. Compounds according to embodiment A36, wherein

• R₅ is indolyl, pyridyl, pyrimidinyl, indazolyl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, or 4 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, —C(O)NR₆R₇, —NR₈R₉, NR₆R₇ C₁-C₄ alkyl, and amidinooxime; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, phenyl C₁-C₄ alkyl, phenyl C₁-C₄ alkoxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃.

Embodiment A39. Compounds according to embodiment A38, wherein

• R₅ is indolyl, pyridyl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, or 4 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, —C(O)NR₆R₇, NR₈R₉, NR₆R₇-C₁-C₄ alkyl-, and amidinooxime; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃.

Embodiment A40. Compounds according to embodiment A36, wherein

• R₅ is indolyl, pyridyl, pyridazinyl, pyrimidinyl, or pyrazinyl, each of which is unsubstituted or substituted with 1, 2, 3, 4 or 5 groups that are independently C₁-C₄ alkyl, halogen, CF₃, OCF₃, —CO₂CH₃, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, —CO₂(C₁-C₅ alkyl), benzyloxy, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl) wherein the alkyl group is optionally substituted with OH or methoxy, —C(O)N(C₁-C₆ alkyl) (C₁-C₆ alkyl) wherein each alkyl group is independently and optionally substituted with OH or methoxy, —C(O)NR₆R₇, NR₈R₉, NR₆R₇ C₁-C₄ alkyl, —C₁-C₄ alkyl-NH₂, —C₁-C₄ alkyl-NH(C₁-C₆ alkyl) wherein each alkyl group is independently and optionally substituted with OH or methoxy, —C₁-C₄ alkyl-N(C₁-C₆ alkyl)(C₁-C₆ alkyl) wherein each alkyl group is independently and optionally substituted with OH or methoxy, and amidinooxime; wherein
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A42. Compounds according to any one of embodiments A37, A38, A39, or A40, wherein

• R₁ is H, halogen, methyl, or carboxaldehyde;
  • R₂ is benzyloxy, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, NR₆R₇(C₁-C₆)alkyl, pyridyl, morpholinyl, thiomorpholinyl, piperazinyl pyridyl(C₁-C₆)alkyl, morpholinyl(C₁-C₆)alkyl, thiomorpholinyl(C₁-C₆)alkyl, or piperazinyl(C₁-C₆)alkyl wherein the pyridyl, morpholinyl, thiomorpholinyl, and piperazinyl rings are optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, or halogen; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl optionally substituted with 1 or two groups that are independently OH, halogen or methoxy, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, benzyl, benzyloxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, CF₃, or OCF₃, and
• R₄ is H, (C₁-C₃)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, —NR₆R₇, NR₆R₇C₁-C₄ alkyl, or hydroxy(C₁-C₃)alkyl.

Embodiment A43. Compounds according to embodiment A42, wherein

• R₁ is H or halogen.

Embodiment A44. Compounds according to embodiment A 18, wherein

• R₅ is phenyl(C₁-C₆)alkyl, (C₁-C₆)alkyl, piperidinyl(C₁-C₆)alkyl, thienyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, naphthyl(C₁-C₆)alkyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, isoindolyl(C₁-C₆) alkyl, indol-2-onyl(C₁-C₆)alkyl, pyridazinyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, benzyloxy, hydroxyalkyl, thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, CF₃, or OCF₃;
    • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl and phenyl C₁-C₆ alkanoyl; and
  • R₉ is aminoalkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, indazolyl, and phenyl C₁-C₄ alkanoyl.

In this embodiment, it is preferred that when R₂ is benzyloxy, R₄ is H, and R₅ is benzyl or methyl, R₁ is not hydrogen; and

• • no more than two of R₁, R₂, R₄, and R₅ are simultaneously hydrogen.

Embodiment A45. Compounds according to embodiment A44, wherein

• R₅ is phenyl(C₁-C₆)alkyl, which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, benzyloxy, thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, CF₃, or OCF₃; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, phenyl C₁-C₄ alkyl, phenyl C₁-C₄ alkoxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
  • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl and phenyl C₁-C₆ alkanoyl; and
  • R₉ is aminoalkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, indazolyl, and phenyl C₁-C₄ alkanoyl.

Embodiment A46. Compounds according to embodiment A45, wherein

• R₅ is phenyl(C₁-C₆)alkyl, which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently CN, halogen, C₁-C₄ alkoxy, C₁-C₄ thioalkoxy, C₁-C₄ haloalkyl, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ haloalkoxy, —C(O)NR₂₀R₂₁, wherein
  • R₂₀ and R₂, are independently H, C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, or
  • R₂₀, R₂₁, and the nitrogen to which they are attached form a piperazinyl, or morpholinyl ring, each of which is optionally substituted with 1 or 2 groups that are independently alkyl or halogen.

Embodiment A47. Compounds according to embodiment A46, wherein

• R₅ is phenyl(C₁-C₄)alkyl, which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently CN, halogen, C₁-C₄ alkoxy, C₁-C₄ haloalkyl, C₁-C₄ alkyl, C₁-C₄ haloalkoxy, —C(O)NR₂₀R₂₁, wherein
  • R₂₀ and R₂, are independently H, C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, or
  • R₂₀, R₂₁, and the nitrogen to which they are attached form a piperazinyl, or morpholinyl ring, each of which is optionally substituted with 1 or 2 groups that are independently alkyl or halogen.

Embodiment A48. Compounds according to embodiment A47, wherein

• R₅ is benzyl or phenethyl, each of which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently CN, halogen, C₁-C₄ alkoxy, CF₃, OCF₃, C₁-C₄ alkyl, —C(O)NR₂₀R₂₁, wherein
  • R₂₀ and R₂, are independently H, C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, or
  • R₂₀, R₂₁, and the nitrogen to which they are attached form a piperazinyl, or morpholinyl ring, each of which is optionally substituted with 1 or 2 groups that are independently alkyl or halogen.

Embodiment A49. Compounds according to embodiment A48, wherein

• R₅ is benzyl or phenethyl, each of which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, methoxy, ethoxy, CF₃, OCF₃, methyl, ethyl, or —C(O)NR₂₀R₂₁, wherein
  • R₂₀ and R₂₁ are independently H, C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl.

Embodiment A50. Compounds according to embodiment A48, wherein

• R₅ is benzyl or phenethyl, each of which is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, methoxy, ethoxy, CF₃, OCF₃, methyl, ethyl, or —C(O)NR₂₀R₂₁, wherein
  • R₂₀, R₂₁, and the nitrogen to which they are attached form a piperazinyl, or morpholinyl ring, each of which is optionally substituted with 1 or 2 groups that are independently alkyl or halogen.

Embodiment A51. Compounds according to embodiment A49, wherein

• • R₅ is substituted on the phenyl ring with 1, 2, 3, 4, or 5 groups and wherein there is a group at the para position of the phenyl.

Embodiment A52. Compounds according to embodiment A43, wherein

• R₅ is piperidinyl(C₁-C₆)alkyl, thienyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆) alkyl, isoindolyl(C₁-C₆)alkyl, indol-2-onyl(C₁-C₆)alkyl, pyridazinyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, halogen, C₁-C₆ alkoxy, C₁-C₆ hydroxyalkyl, benzyloxy, C₁-C₆ thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, CF₃, or OCF₃;
  • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl and phenyl C₁-C₆ alkanoyl; and
  • R₉ is aminoalkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, indazolyl, and phenyl C₁-C₄ alkanoyl.

In this embodiment, it is preferred that when R₂ is benzyloxy, R₄ is H, and R₅ is benzyl or methyl, R₁ is not hydrogen; and

• • no more than two of R₁, R₂, R₄, and R₅ are simultaneously hydrogen.

Embodiment A53. Compounds according to embodiment A52, wherein R₅ is piperidinyl(C₁-C₄)alkyl, thienyl(C₁-C₄)alkyl, indolyl(C₁-C₄)alkyl, pyridyl(C₁-C₄)alkyl, pyrimidyl(C₁-C₄)alkyl, or pyrazinyl(C₁-C₄)alkyl, each of which is unsubstituted.

Embodiment A54. Compounds according to embodiment A52, wherein

• R₅ is indolyl(C₁-C₄)alkyl, pyrimidyl(C₁-C₄)alkyl, or pyrazinyl(C₁-C₄)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, or 4 groups that are independently C₁-C₆ alkyl, halogen, C₁-C₆ alkoxy, C₁-C₆ hydroxyalkyl, benzyloxy, C₁-C₆ thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, amidino, —C(O)NR₂₀R₂₁, CF₃, or OCF₃; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, benzyl, benzyloxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
    • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl and phenyl C₁-C₄ alkanoyl; and
    • R₉ is aminoalkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, indazolyl, and phenyl C₁-C₄ alkanoyl;
  • R₂₀ and R₂₁ are independently H, C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, or
  • R₂₀, R₂₁, and the nitrogen to which they are attached form a piperazinyl, or morpholinyl ring, each of which is optionally substituted with 1 or 2 groups that are independently alkyl or halogen.

Embodiment A55. Compounds according to embodiment A54, wherein

• R₅ is indolyl(C₁-C₄)alkyl, or pyrazinyl(C₁-C₄)alkyl, wherein each of the above is unsubstituted or substituted with 1, 2, 3, or 4 groups that are independently C₁-C₆ alkyl, halogen, C₁-C₆ alkoxy, C₁-C₆ hydroxyalkyl, benzyloxy, C₁-C₆ thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂H, CN, —C(O)NR₂₀R₂₁, CF₃, or OCF₃; wherein
  • R₂₀ and R₂, are independently H, C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, or
  • R₂₀, R₂₁, and the nitrogen to which they are attached form a piperazinyl, or morpholinyl ring, each of which is optionally substituted with 1 or 2 groups that are independently alkyl or halogen.

Embodiment A56. Compounds according to embodiment A52, wherein

• R₅ is isoquinolinyl, isoindolyl, indol-2-onyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆) alkyl, isoindolyl(C₁-C₆)alkyl, indol-2-onyl(C₁-C₆)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, halogen, C₁-C₆ alkoxy, C₁-C₆ hydroxyalkyl, benzyloxy, C₁-C₆ thioalkoxy, —CO₂(C₁-C₅ alkyl), CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, CF₃, or OCF₃.

Embodiment A57. Compounds according to embodiment A1, wherein

• R₁ is H, halogen, methyl, ethyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, or carboxaldehyde;
  • R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, or NR₆R₇—(C₁-C₆ alkyl)-; and
• R₄ is H, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, or hydroxy(C₁-C₄)alkyl;
• R₅ is C₃-C₇ cycloalkyl or C₃-C₇ cycloalkylalkyl, each of which is optionally substituted with 1 or 2 groups that are independently alkyl, alkoxy, halogen, —NR₆R₇, or NR₆R₇—(C₁-C₆ alkyl)-, wherein each of the alkyl groups is optionally substituted with 1 or 2 groups that are independently OH, methoxy, NH₂, or halogen.

Embodiment A58. Compounds according to embodiment A57, wherein

• R₅ is C₃-C₇ cycloalkyl or C₃-C₇ cycloalkyl C₁-C₄ alkyl, each of which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, —NR₆R₇, or NR₆R₇—(C₁-C₆ alkyl)- wherein each of the alkyl groups is optionally substituted with 1 or 2 groups that are independently OH, methoxy, or NH₂;
• R₆ and R₇ are independently at each occurrence H, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ alkoxy, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkanoyl, benzyl, benzyloxy, or phenyl C₁-C₄ alkanoyl, wherein each is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, CF₃, or OCF₃; or
• R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A59. Compounds according to embodiment A58, wherein

• R₁ is H, halogen, methyl, ethyl;
• R₂ is benzyloxy, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, amino, mono or dialkylamino, —NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, or NR₆R₇—(C₁-C₆ alkyl)-; and
• R₄ is H, methyl, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇ or hydroxy(C₁-C₂)alkyl.

Embodiment A60. Compounds according to embodiment A59, wherein

• R₂ is substituted with two halogens and is further optionally substituted with 1 or 2 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, amino, mono or dialkylamino, —NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, or NR₆R₇—(C₁-C₆ alkyl).

Embodiment A61. Compounds according to embodiment A1, wherein

• R₅ is H, alkyl optionally substituted with 1, 2, or 3 groups that are independently phenylalkoxycarbonyl, —NR₈R₉, halogen, —C(O)NR₈R₉, alkoxycarbonyl, or alkanoyl, alkoxyalkyl optionally substituted with one trimethylsilyl group, alkoxycarbonyl, amino, hydroxyalkyl, alkenyl optionally substituted with alkoxycarbonyl, alkynyl, —SO₂-alkyl, or alkoxy optionally substituted with one trimethylsilyl group, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, phenylalkoxy, thioalkoxy, —SO₂alkyl, alkoxycarbonyl, phenylalkoxycarbonyl, CO₂H, CN, OH, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, hydroxyalkyl, carboxaldehyde, —NR₆R₇, haloalkyl, or haloalkoxy;
    • wherein R₈ is hydrogen, alkyl, alkanoyl, phenylalkyl and arylalkanoyl; and
    • wherein R₉ is alkyl, alkanoyl, phenylalkyl, heteroaryl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, and arylalkanoyl.

In this embodiment, it is preferred that when R₂ is benzyloxy, R₄ is H, and R₅ is benzyl or methyl, R₁ is not hydrogen; and

• • no more than two of R₁, R₂, R₄, and R₅ are simultaneously hydrogen.

Embodiment A62. Compounds according to embodiment A1, wherein

• R₅ is H, alkyl optionally substituted with 1, 2, or 3 groups that are independently phenylalkoxycarbonyl, —NR₈R₉, halogen, —C(O)NR₈R₉, alkoxycarbonyl, or alkanoyl, alkoxyalkyl optionally substituted with one trimethylsilyl group, alkoxycarbonyl, amino, hydroxyalkyl, alkenyl optionally substituted with alkoxycarbonyl, alkynyl, —SO₂-alkyl, alkoxy optionally substituted with one trimethylsilyl group, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, phenylalkoxy, thioalkoxy, —SO₂alkyl, alkoxycarbonyl, phenylalkoxycarbonyl, CO₂H, CN, OH, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, hydroxyalkyl, carboxaldehyde, —NR₆R₇, haloalkyl, or haloalkoxy;
    • wherein R₈ is hydrogen, alkyl, alkanoyl, phenylalkyl and arylalkanoyl; and
    • wherein R₉ is alkyl, alkanoyl, phenylalkyl, heteroaryl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, and arylalkanoyl.

In this embodiment, it is preferred that when R₂ is benzyloxy, R₄ is H, and R₅ is benzyl or methyl, R₁ is not hydrogen; and

• • no more than two of R₁, R₂, R₄, and R₅ are simultaneously hydrogen.

Embodiment A63. Compounds according to embodiment A62, wherein

• R₁ is H, halogen, methyl, ethyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, or NR₆R₇—(C₁-C₆ alkyl)-; and
• R₄ is H, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, or hydroxy(C₁-C₄)alkyl.

Embodiment A64. Compounds according to embodiment A63, wherein

• R₅ is H, alkyl optionally substituted with 1, 2, or 3 groups that are independently phenylalkoxycarbonyl, —NR₈R₉, halogen, —C(O)NR₈R₉, alkoxycarbonyl, or alkanoyl, alkoxyalkyl optionally substituted with one trimethylsilyl group, alkoxycarbonyl, amino, hydroxyalkyl, alkenyl optionally substituted with alkoxycarbonyl, alkynyl, —SO₂-alkyl, alkoxy optionally substituted with one trimethylsilyl group, wherein
  • wherein R₈ is hydrogen, C₁-C₄ alkyl, C₁-C₄ alkanoyl, phenyl C₁-C₄ alkyl and phenyl C₁-C₄ alkanoyl;
  • wherein R₉ is C₁-C₄ alkyl, C₁-C₄ alkanoyl, phenyl C₁-C₄ alkyl, pyridyl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, and phenyl C₁-C₄ alkanoyl.

Embodiment A65. Compounds according to embodiment A64, wherein

• R₅ is C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently phenyl C₁-C₄ alkoxycarbonyl, NH₂, mono C₁-C₄ alkylamino, di C₁-C₄ alkylamino, halogen, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl) wherein the alkyl is optionally substituted with OH, NH₂, or methoxy, —C(O)N(C₁-C₆ alkyl) (C₁-C₆ alkyl) wherein each alkyl is optionally substituted with OH, NH₂, or methoxy, C₁-C₄ alkoxycarbonyl, and C₁-C₄ alkanoyl, or
• R₅ is C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, amino, C₁-C₄ hydroxyalkyl, C₂-C₄ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkynyl, —SO₂—C₁-C₄ alkyl, or C₁-C₄ alkoxy.

Embodiment A66. A compound of the formula or a pharmaceutically acceptable salt thereof, wherein

• R₁ is halogen, NO₂, alkyl, carboxaldehyde, hydroxyalkyl, arylalkoxy, arylalkyl, CN, aryl, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, or arylalkanoyl,
  • wherein the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, (C₁-C₄)alkyl, (C₁-C₄)alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO₂H;
  • wherein the alkyl portion of the alkyl, hydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl groups is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkoxy, C₁-C₄ alkoxycarbonyl, or spirocyclopropyl;
• R₂ is aryl, heteroaryl, arylalkenyl, arylalkoxy, aryloxyalkyl, arylalkyl, OH, alkynyl, aryloxy, aryloxyalkyl, arylthioalkoxy, alkoxy, —OC(O)NH(CH₂)_naryl, —OC(O)N(alkyl)(CH₂)_naryl, —OSO₂(C₁-C₆)alkyl, —OSO₂aryl, alkyl, alkoxyalkoxy, NR₈R₉, or CO₂H, wherein
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, alkoxy, alkoxycarbonyl, CN, NR₆R₇, haloalkyl, haloalkoxy, alkyl, heteroaryl, heteroarylalkyl, NR₆R₇—(C₁-C₆ alkyl)-, phenyl, —SO₂-phenyl wherein the phenyl groups are optionally substituted with 1, 2, or 3 groups that are independently halogen or NO₂; or —OC(O)NR₆R₇, wherein
  • R₆ and R₇ are independently at each occurrence H, alkyl, alkoxy, alkoxyalkyl, alkoxycarbonyl, —SO₂-alkyl, OH, hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, heteroarylalkyl, alkanoyl, arylalkyl, arylalkoxy, or arylalkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, heterocycloalkyl, OH, SH, C₃-C₆ cycloalkyl, NH₂, NH(alkyl), N(alkyl)(alkyl), —O-alkanoyl, alkyl, haloalkyl, or haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
  • R at each occurrence is independently H or C₁-C₆ alkyl;
  • R₃₀ is C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
• R₄ is H, alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, arylalkoxy, arylalkyl, hydroxyalkyl, haloalkyl, alkoxy, carboxaldehyde, CO₂H, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the aryl portion of arylalkoxy, arylalkyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, haloalkyl, or haloalkoxy; and
• R₅ is H, arylalkyl, alkyl, aryl, alkoxy, heterocycloalkylalkyl, heteroarylalkyl, heterocycloalkyl, cycloalkyl, cycloalkylalkyl, -alkyl-S-aryl, -alkyl-SO₂-aryl, —(C₁-C₄)alkyl-C(O)-heterocycloalkyl, —SO₂-aryl, or heteroaryl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, aryl, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, OH, CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, amidino, hydroxyalkyl, —SO₂alkyl, —SO₂H, —SO₂NR₆R₇, —NR₆R₇, alkanoyl wherein the alkyl portion is optionally substituted with OH, halogen or alkoxy, haloalkyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, —O—CH₂—O, —O—CH₂CH₂—O—, or haloalkoxy; wherein
    • R₈ at each occurrence is independently hydrogen, alkyl, alkanoyl, arylalkyl and arylalkanoyl wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl; and
    • R₉ at each occurrence is independently alkyl, alkanoyl, arylalkyl cycloalkyl, alkenyl, heteroaryl, cycloalkylalkyl, arylalkanoyl, —SO₂-phenyl, and aryl wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl;
    • R₁₅ is H or C₁-C₆ alkyl;
    • R₁₆ and R₁₇ are independently H or C₁-C₆ alkyl; or
    • R₁₆, R₁₇, and the nitrogen to which they are attached form a morpholinyl ring; and
    • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that:

• R₆ and R₇ are not simultaneously OH;
• R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl);
• when R₂ is OH, R₄ is methyl and R₅ is phenyl, R₁ is not acetyl; and
• R₄ and R₅ are not simultaneously hydrogen.

Embodiment A71. Compounds according to embodiment A66 wherein

• R₁ is halogen, C₁-C₆ alkyl, phenyl, carboxaldehyde, C₁-C₆ hydroxyalkyl, phenyl C₁-C₆ alkoxy, phenyl C₁-C₆ alkyl, CN, C₁-C₆ alkanoyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ haloalkyl, or phenyl C₁-C₆ alkanoyl,
  • wherein the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, (C₁-C₄)alkyl, (C₁-C₄)alkoxy, nitro, CN, C₁-C₄ haloalkyl, C₁-C₄ haloalkoxy or CO₂H;
  • wherein the above alkyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy,
• R₂ is phenylalkoxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, phenylthio(C₁-C₄)alkoxy, alkoxy, alkenyl, phenethyl, —OC(O)NH(CH₂)_nphenyl, —OC(O)N(alkyl)(CH₂)_nphenyl, alkyl, alkoxyalkoxy, NR₈R₉, pyridyl, pyrimidyl, pyridazyl, pyrazolyl, imidazolyl, pyrrolyl, tetrahydroquinolinyl, amino, tetrahydroisoquinolinyl, tetrazolyl, pyrazinyl, benzimidazolyl, triazinyl, tetrahydrofuryl, piperidinyl, hexahydropyrimidinyl, thiazolyl, thienyl, or CO₂H, wherein
  • n is 0, 1, 2, or 3;
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, haloalkyl, haloalkoxy, alkyl, thienyl, pyridyl, or phenyl optionally substituted with 1, 2, or 3 halogens;
  • R₆ and R₇ are independently at each occurrence H, alkyl, alkoxy, alkoxyalkyl, hydroxyalkyl, alkoxycarbonyl, —(C₁-C₄)alkyl-CO₂-alkyl, alkanoyl, phenylalkyl, phenylalkoxy, or phenylalkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, alkoxy, NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), alkyl, CF₃ or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
• R₄ is H, alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenylalkoxy, phenylalkyl, hydroxyalkyl, carboxaldehyde, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, haloalkyl, or haloalkoxy; and
• R₅ is benzyl, phenethyl, (C₁-C₆)alkyl, phenyl, naphthyl, alkoxy, piperidinyl, pyrrolidinyl, imidazolidinyl, piperazinyl, isoquinolinyl, tetrahydroisoquinolinyl, indolyl, 1H-indazolyl, pyridyl, pyrimidyl, pyridazyl, pyrazinyl, piperidinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, piperazinyl(C₁-C₆)alkyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, pyridazyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, tetrahydroisoquinolinyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, or 1H-indazolyl(C₁-C₆)alkyl, and wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, hydroxyalkyl, phenylalkoxy; thioalkoxy, alkoxycarbonyl, phenylalkoxycarbonyl, OH, CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, piperazinyl, morpholinyl, —SO₂ (C₁-C₆)alkyl, —SO₂NH₂, —SO₂NH(C₁-C₆)alkyl, —SO₂N(C₁-C₆)alkyl(C₁-C₆)alkyl, haloalkyl, or haloalkoxy.

In this embodiment, it is preferred that when R₂ is OH, P4 is methyl and R₅ is phenyl, R₁ is not acetyl; and

• R₄ and R₅ are not simultaneously hydrogen.

Embodiment A72. Compounds according to embodiment A71 wherein

• R₁ is halogen, alkyl, carboxaldehyde, hydroxyalkyl, phenylalkoxy, phenyl, benzyl, phenethyl, phenpropyl, phenbutyl, CN, (C₂-C₆)alkanoyl, haloalkyl, or phenylCO—, phenylCH₂CO—, phenylCH₂CH₂CO—,
  • wherein the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, (C₁-C₄)alkyl, (C₁-C₄)alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO₂H;
  • wherein the above alkyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy,
• R₂ is benzyloxy, phenethyloxy, phenpropyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, phenylthio(C₁-C₄)alkoxy, NR₈R₉, (C₁-C₆)alkyl, alkynyl, phenethyl, —OC(O)N(CH₃)CH₂phenyl, alkoxyalkoxy, pyridyl, pyrimidyl, pyridazyl, pyrazolyl, imidazolyl, pyrrolyl, pyrazinyl, piperidinyl, hexahydropyrimidinyl, benzimidazolyl, or thienyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, CF₃, OCF₃, (C₁-C₄)alkyl, thienyl, pyridyl, or phenyl optionally substituted with 1, 2, or 3 halogens;
  • R₆ and R₇ are independently at each occurrence H, (C₁-C₆)alkyl, (C₁-C₆)alkoxy, (C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₁-C₆)alkoxycarbonyl, hydroxy(C₁-C₆)alkyl, —(C₁-C₄)alkyl-CO₂-alkyl, (C₁-C₆)alkanoyl, phenyl(C₁-C₆)alkyl, phenyl(C₁-C₆)alkoxy, or phenyl(C₁-C₆)alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, (C₁-C₆)alkoxy, NH₂, OH, SH, C₃-C₆ cycloalkyl, (C₁-C₆)alkyl, CF₃ or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
• R₄ is H, alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, benzyloxy, phenethyloxy, phenpropyloxy, benzyl, phenethyl, phenpropyl, hydroxyalkyl, halo(C₁-C₄)alkyl, carboxaldehyde, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, CF₃ or OCF₃; and
• R₅ is benzyl, phenethyl, phenpropyl, phenbutyl, (C₁-C₆)alkyl, phenyl, piperidinyl, pyrrolidinyl, imidazolidinyl, piperidinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, pyridyl, pyrimidyl, pyridazyl, pyrazinyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, pyridazyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆)alkyl wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, haloalkyl, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, carboxaldehyde, morpholinyl, SO₂NH₂, SO₂NH(alkyl), SO₂N(alkyl)(alkyl), alkoxy, hydroxyalkyl, benzyloxy, thioalkoxy, OH, CO₂H, CN, —CO₂(C₁-C₅ alkyl), phenylalkoxycarbonyl, amidinooxime, amidino, —C(O)NR₆R₇, CF₃, CF₂CF₃, ClCH₂, or OCF₃.

In this embodiment, it is preferred that when R₂ is OH, R₄ is methyl and R₅ is phenyl, R₁ is not acetyl.

Embodiment A73. Compounds according to embodiment A72 wherein

• R₁ is halogen, alkyl, carboxaldehyde, hydroxy(C₁-C₄)alkyl, phenylalkoxy, benzyl, phenethyl, —C(O)CH₃, phenylCO—, or phenylCH₂CO—,
  • wherein the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, (C₁-C₄)alkyl, (C₁-C₄)alkoxy, nitro, CN, CF₃, or OCF₃;
  • wherein the above alkyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy;
• R₂ is benzyloxy, phenethyloxy, phenpropyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, phenethyl, NR₈R₉, —S-benzyl, or (C₁-C₆)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, CF₃, OCF₃, alkyl, thienyl, or pyridyl;
  • R₆ and R₇ are independently at each occurrence H, (C₁-C₆)alkyl, (C₁-C₆)alkoxy, (C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₁-C₆)alkoxycarbonyl, hydroxy(C₁-C₆)alkyl, —(C₁-C₄)alkyl-CO₂-alkyl, (C₁-C₆)alkanoyl, phenyl(C₁-C₆)alkyl, phenyl(C₁-C₆)alkoxy, or phenyl(C₁-C₆)alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, (C₁-C₆)alkoxy, NH₂, OH, SH, C₃-C₆ cycloalkyl, (C₁-C₆)alkyl, CF₃ or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
• R₄ is H, alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, benzyloxy, phenethyloxy, phenpropyloxy, benzyl, or hydroxyalkyl, wherein
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, CF₃ or OCF₃; and
• R₅ is benzyl, phenethyl, phenpropyl, phenbutyl, (C₁-C₆)alkyl, phenyl, pyridyl, pyrazinyl, pyrimidinyl, pyrazinyl(C₁-C₆)alkyl, pyrimidinyl(C₁-C₆)alkyl, or pyridyl(C₁-C₄)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, haloalkyl, morpholinyl, —SO₂ (C₁-C₆)alkyl, —SO₂NH₂, —SO₂NH(C₁-C₆), —SO₂N(C₁-C₆)(C₁-C₆), (C₁-C₄)alkoxy, phenyl(C₁-C₄)alkoxy, thio(C₁-C₄)alkoxy, (C₁-C₄)alkoxycarbonyl, OH, CO₂H, CN, amidinooxime, amidino, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, hydroxyalkyl, CONR₆R₇, CF₃, or OCF₃.

Embodiment A74. Compounds according to embodiment A73 wherein

• R₁ is halogen, alkyl, carboxaldehyde, or hydroxyalkyl;
• R₂ is benzyloxy, phenethyloxy, phenpropyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, phenethyl, phenylthioalkoxy, or (C₁-C₆)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, CF₃, OCF₃, alkyl, thienyl, or pyridyl;
• R₄ is H, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, benzyloxy, or phenethyloxy, wherein
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, (C₁-C₄)alkoxy, (C₁-C₄)alkyl, nitro, CF₃ or OCF₃; and
• R₅ is benzyl, phenethyl, (C₁-C₆)alkyl, phenyl, indazolyl, or pyridyl, wherein each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently (C₁-C₄)alkyl, halogen, OH, CO₂H, CN, (C₁-C₄)alkoxy, —C(O)pyrrolidine, —SO₂ (C₁-C₆)alkyl, benzyloxy, —CO₂(C₁-C₅ alkyl), amidino, thio(C₁-C₄)alkoxy, amidinooxime, CF₃, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, CONR₆R₇, or OCF₃.

Embodiment A75. Compounds according to embodiment A74 wherein

• R₁ is chloro, bromo, iodo, methyl, C₂-C₃ alkenyl, C₂-C₃ alkynyl; and
• R₅ is benzyl, phenethyl, phenpropyl, phenyl, or pyridyl, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently alkyl, OH, halogen, alkoxy, NH₂, NH(C₁-C₆)alkyl, N(C₁-C₆)alkyl(C₁-C₆)alkyl, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, CONR₆R₇, and amidinooxime; wherein
  • R₆ and R₇ are independently H, C₁-C₄ alkyl, C₁-C₆ alkanoyl, wherein the alkyl and alkanoyl groups are optionally substituted with 1, 2, or 3 groups that are independently OH, halogen, or C₃-C₇ cyclopropyl.

Embodiment A76. Compounds according to embodiment A75 wherein

• R₂ is benzyloxy, phenethyl, phenyloxy(C₁-C₆)alkyl, or phenethyloxy, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, CF₃, OCF₃, or (C₁-C₄)alkyl.

Embodiment A77. Compounds according to embodiment A66, wherein

• R₅ is benzyl, phenethyl, thienyl(C₁-C₆ alkyl), piperidinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, piperazinyl(C₁-C₆)alkyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, pyridazyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, tetrahydroisoquinolinyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, or 1H-indazolyl(C₁-C₆)alkyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently (C₁-C₆)alkyl, halogen, (C₁-C₆)alkoxy, (C₁-C₆)hydroxyalkyl, phenyl(C₁-C₆)alkoxy, (C₁-C₆)thioalkoxy, (C₁-C₆)alkoxycarbonyl, phenyl(C₁-C₆)alkoxycarbonyl, OH, CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, piperazinyl, morpholinyl, —SO₂ (C₁-C₆)alkyl, —SO₂NH₂, —SO₂NH(C₁-C₆)alkyl, —SO₂N(C₁-C₆)alkyl(C₁-C₆)alkyl, (C₁-C₄)haloalkyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, —O—CH₂—O, —O—CH₂CH₂—O—, or (C₁-C₄)haloalkoxy; wherein
    • R₆ and R₇ are independently at each occurrence H, (C₁-C₆)alkyl, (C₁-C₆)alkoxy, (C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₁-C₆)alkoxycarbonyl, (C₁-C₆)hydroxyalkyl, —(C₁-C₄)alkyl-CO₂—(C₁-C₆)alkyl, (C₁-C₆)alkanoyl, phenyl(C₁-C₆)alkyl, phenyl(C₁-C₆)alkoxy, or phenyl(C₁-C₆)alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, (C₁-C₄)alkoxy, NH₂, OH, SH, C₃-C₆ cycloalkyl, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), (C₁-C₄)alkyl, CF₃ or OCF₃; or
    • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen; and
    • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH; and R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment A78. Compounds according to embodiment A77, wherein

• R₁ is halogen, methyl, ethyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, or pyridyl; and
• R₄ is H, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, or hydroxy(C₁-C₄)alkyl.

Embodiment A79. Compounds according to embodiment A78, wherein

• R₅ is benzyl, or phenethyl, wherein each is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently (C₁-C₆)alkyl, halogen, (C₁-C₆)alkoxy, (C₁-C₆)hydroxyalkyl, phenyl(C₁-C₆)alkoxy, (C₁-C₆)thioalkoxy, (C₁-C₆)alkoxycarbonyl, phenyl(C₁-C₆)alkoxycarbonyl, OH, CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇amidino, piperazinyl, morpholinyl, —SO₂ (C₁-C₆)alkyl, —SO₂NH₂, —SO₂NH(C₁-C₆)alkyl, —SO₂N(C₁-C₆)alkyl(C₁-C₆)alkyl, (C₁-C₄)haloalkyl, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, —O—CH₂—O, —O—CH₂CH₂—O—, or (C₁-C₄)haloalkoxy; wherein
  • R₆ and R₇ are independently at each occurrence H, (C₁-C₆)alkyl, (C₁-C₆)alkoxy, (C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₁-C₆)alkoxycarbonyl, (C₁-C₆)hydroxyalkyl, —(C₁-C₄)alkyl-CO₂—(C₁-C₆)alkyl, (C₁-C₆)alkanoyl, phenyl(C₁-C₆)alkyl, phenyl(C₁-C₆)alkoxy, or phenyl(C₁-C₆)alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, (C₁-C₄)alkoxy, NH₂, OH, SH, C₃-C₆ cycloalkyl, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), (C₁-C₄)alkyl, CF₃ or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen; and
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, amino C₁-C₆ alkyl, or mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH; and

• • R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment A80. Compounds according to embodiment A79, wherein

• R₅ is benzyl or phenethyl, wherein each is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₈R₉, halogen, C₁-C₆ alkoxy, CO₂H, —(C₁-C₄ alkyl)-CO₂H, C₁-C₆ thioalkoxy, amidinooxime, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-C₁-C₆ alkoxycarbonyl, C₁-C₆ hydroxyalkyl, —(C₁-C₄ alkyl)-CN, CN, phenyl C₁-C₆ alkoxy, OH, C₁-C₄ haloalkyl, C₁-C₄ haloalkoxy, NR₆R₇—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, amidinooxime, —SO₂(C₁-C₆ alkyl), —O—CH₂—O—, —O—CH₂CH₂—O—, phenyl C₁-C₄ alkoxy, or phenyl; wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl, thiomorpholinyl, ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen,
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH; and

• R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment A81. Compounds according to embodiment A80, wherein

• R₅ is benzyl or phenethyl, wherein each is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, halogen, C₁-C₆ alkoxy, CO₂H, —(C₁-C₄ alkyl)-CO₂H, C₁-C₆ thioalkoxy, amidinooxime, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-C₁-C₆ alkoxycarbonyl, C₁-C₆ hydroxyalkyl, —(C₁-C₄ alkyl)-CN, CN, phenyl C₁-C₆ alkoxy, OH, C₁-C₄ haloalkyl, C₁-C₄ haloalkoxy, NR₆R₇—(C₁-C₆ alkyl)-, NR₈R₉, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, amidinooxime, —SO₂(C₁-C₆ alkyl), —O—CH₂—O—, —O—CH₂CH₂—O—, phenyl C₁-C₄ alkoxy, or phenyl; wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃; and
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH; and

• • R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment A82. Compounds according to embodiment A81, wherein

• R₅ is benzyl which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, halogen, C₁-C₄ alkoxy, CO₂H, C₁-C₄ thioalkoxy, C₁-C₄ alkoxycarbonyl, C₁-C₆ hydroxyalkyl, CN, OH, NR₆R₇—(C₁-C₆ alkyl)-, NR₈R₉, —SO₂(C₁-C₆ alkyl), or benzyloxy; wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH; and

• • R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment A83. Compounds according to embodiment A82, wherein

• R₅ is benzyl which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, halogen, C₁-C₄ alkoxy, C₁-C₄ thioalkoxy, C₁-C₄ alkoxycarbonyl, C₁-C₆ hydroxyalkyl, CN, NR₈R₉, or NR₆R₇—(C₁-C₆ alkyl)-; wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, or C₁-C₄ alkoxy C₁-C₄ alkyl each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH.

Embodiment A84. Compounds according to embodiment A83, wherein the R₅ group is disubstituted with two groups that are meta to each other.

Embodiment A86. Compounds according to embodiment A80, wherein

• R₅ is benzyl which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, halogen, C₁-C₄ alkoxy, CO₂H, —(C₁-C₄ alkyl)-CO₂H, —(C₁-C₄ alkyl)-C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-CN, CN, phenyl C₁-C₆ alkoxy, CF₃, OCF₃, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, amidinooxime, —O—CH₂—O—, —O—CH₂CH₂—O—, or phenyl; wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₄ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₄ alkyl)alkyl, N(C₁-C₄ alkyl)(C₁-C₄ alkyl) C₁-C₄ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₄ alkoxy C₁-C₄ alkyl, or OH, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃; and
  • R₁₈ is C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₄ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH.

Embodiment A87. Compounds according to embodiment A80, wherein

• R₅ is benzyl or phenethyl, wherein each is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, halogen, C₁-C₆ alkoxy, CO₂H, —(C₁-C₄ alkyl)-CO₂H, C₁-C₆ thioalkoxy, amidinooxime, C₁-C₆ alkoxycarbonyl, —(C₁-C₄ alkyl)-C₁-C₆ alkoxycarbonyl, C₁-C₆ hydroxyalkyl, —(C₁-C₄ alkyl)-CN, CN, phenyl C₁-C₆ alkoxy, OH, C₁-C₄ haloalkyl, C₁-C₄ haloalkoxy, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, amidinooxime, —SO₂(C₁-C₆ alkyl), —O—CH₂—O—, —O—CH₂CH₂—O—, phenyl C₁-C₄ alkoxy, or phenyl; wherein
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl, thiomorpholinyl, ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen,
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH; and

• • R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment A88. Compounds according to embodiment A87, wherein

• R₅ is benzyl which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —C(O)NR₆R_7, —(C₁-C₄alkyl)-C(O)NR₆R_7, halogen, C₁-C₄ alkoxy, CO₂H, C₁-C₄ thioalkoxy, C₁-C₄ alkoxycarbonyl, C₁-C₆ hydroxyalkyl, CN, OH, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —SO₂(C₁-C₆ alkyl), or benzyloxy; and wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, or —SO₂(C₁-C₆ alkyl), each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH; and

• • R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment A89. Compounds according to embodiment A80, wherein

• R₅ is benzyl which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, NR₈R₉, halogen, C₁-C₄ alkoxy, C₁-C₄ thioalkoxy, C₁-C₄ alkoxycarbonyl, C₁-C₆ hydroxyalkyl, or CN; wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, or C₁-C₄ alkoxy C₁-C₄ alkyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH.

Embodiment A90. Compounds according to embodiment A89, wherein

• the R₅ group is disubstituted with two groups that are meta to each other.

Embodiment A91. Compounds according to embodiment A78, wherein

• R₅ is phenyl, which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), NR₈R₉, C₁-C₆ hydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂H, OH, C₁-C₆ alkoxycarbonyl, carboxaldehyde, C₁-C₄ haloalkyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈; wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or C₁-C₆ alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen,
  • R₁₅ is H or C₁-C₆ alkyl;
  • R₁₆ and R₁₇ are independently H or C₁-C₆ alkyl; or
  • R₁₆, R₁₇, and the nitrogen to which they are attached form a morpholinyl ring;
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH.

Embodiment A92. Compounds according to embodiment A91, wherein

• R₅ is phenyl, which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —(C₁-C₄ alkyl)-C(O)NR₆R_7, —C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), NR₈R₉, C₁-C₆ hydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂H, OH, C₁-C₆ alkoxycarbonyl, carboxaldehyde, C₁-C₄ haloalkyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈; wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or C₁-C₆ alkanoyl each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃;
  • R₁₅ is H or C₁-C₆ alkyl;
  • R₁₆ and R₁₇ are independently H or C₁-C₆ alkyl; or
  • R₁₆, R₁₇, and the nitrogen to which they are attached form a morpholinyl ring;
  • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

Embodiment A93. Compounds according to embodiment A92, wherein

• R₁ is halogen, methyl, ethyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, or NR₆R₇—(C₁-C₆ alkyl)-; and
• R₄ is H, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, or hydroxy(C₁-C₄)alkyl.

Embodiment A94. Compounds according to embodiment A93, wherein

• R₅ is phenyl, which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R_7, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂H, OH, C₁-C₆ alkoxycarbonyl, carboxaldehyde, C₁-C₄ haloalkyl, wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or C₁-C₆ alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, OH, SH, C₃-C₆ cycloalkyl, C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, CF₃, or OCF₃.

Embodiment A101. Compounds according to embodiment A66, wherein

• R₅ is thienyl(C₁-C₆ alkyl), piperidinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, piperazinyl(C₁-C₆)alkyl, pyridyl(C₁-C₆)alkyl, pyrimidyl(C₁-C₆)alkyl, pyridazyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, tetrahydroisoquinolinyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, 1H-indazolyl(C₁-C₆)alkyl, dihydroindolonyl(C₁-C₆ alkyl), indolinyl(C₁-C₆ alkyl), dihydroisoindolyl(C₁-C₆ alkyl), dihydrobenzimdazolyl(C₁-C₆ alkyl), or dihydrobenzoimidazolonyl(C₁-C₆ alkyl), wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently (C₁-C₆)alkyl, halogen, (C₁-C₆)alkoxy, (C₁-C₆)hydroxyalkyl, phenyl(C₁-C₆)alkoxy, (C₁-C₆)thioalkoxy, (C₁-C₆)alkoxycarbonyl, phenyl(C₁-C₆)alkoxycarbonyl, OH, CO₂H, CN, amidinooxime, NR₈R₉, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, amidino, piperazinyl, morpholinyl, —SO₂ (C₁-C₆)alkyl, —SO₂NH₂, —SO₂NH(C₁-C₆)alkyl, —SO₂N(C₁-C₆)alkyl(C₁-C₆)alkyl, (C₁-C₄)haloalkyl, —(C₁-C₄ alkyl)-NR₁₅C(O)NR₁₆R₁₇, —(C₁-C₄ alkyl)-NR₁₅C(O)R₁₈, —O—CH₂—O, —O—CH₂CH₂—O—, or (C₁-C₄)haloalkoxy; wherein
    • R₆ and R₇ are independently at each occurrence H, (C₁-C₆)alkyl, (C₁-C₆)alkoxy, (C₁-C₆)alkoxy(C₁-C₆)alkyl, (C₁-C₆)alkoxycarbonyl, (C₁-C₆)hydroxyalkyl, —(C₁-C₄)alkyl-CO₂—(C₁-C₆)alkyl, (C₁-C₆)alkanoyl, phenyl(C₁-C₆)alkyl, phenyl(C₁-C₆)alkoxy, or phenyl(C₁-C₆)alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, (C₁-C₄)alkoxy, OH, SH, C₃-C₆ cycloalkyl, NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), (C₁-C₄)alkyl, CF₃ or OCF₃; or
    • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen; and
    • R₁₈ is C₁-C₆ alkyl optionally substituted with —O—(C₂-C₆ alkanoyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl; amino C₁-C₆ alkyl, mono or dialkylamino C₁-C₆ alkyl.

In this embodiment, it is preferred that R₆ and R₇ are not simultaneously OH; and

• • R₆ and R₇ are not simultaneously —SO₂(C₁-C₆ alkyl).

Embodiment A102. Compounds according to embodiment A10, wherein

• R₁ is halogen, methyl, ethyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, or NR₆R₇—(C₁-C₆ alkyl)-; and
• R₄ is H, (C₁-C₄)alkyl optionally substituted with one or two groups that are independently CO₂H, —CO₂alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, or hydroxy(C₁-C₄)alkyl.

Embodiment A103. Compounds according to embodiment A102, wherein

• R₅ is thienyl(C₁-C₆ alkyl), indolyl(C₁-C₆ alkyl), pyridinyl(C₁-C₆ alkyl), piperazinyl(C₁-C₆ alkyl), or pyrazinyl(C₁-C₆ alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, C₁-C₆ alkoxycarbonyl, —NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, haloalkyl, C₁-C₆ alkanoyl,
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkoxycarbonyl, halogen, C₃-C₆ cycloalkyl, OH, SH, or C₁-C₄ alkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A104. Compounds according to embodiment A103, wherein

• R₅ is thienyl(C₁-C₆ alkyl), indolyl(C₁-C₆ alkyl), pyridinyl(C₁-C₆ alkyl), piperazinyl(C₁-C₆ alkyl), or pyrazinyl(C₁-C₆ alkyl).

Embodiment A105. Compounds according to embodiment A103, wherein

• R₄ is H, methyl, ethyl, or —CH₂OH;
• R₅ is pyridinyl(C₁-C₆ alkyl), or pyrazinyl(C₁-C₆ alkyl) each of which is optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R_7, C₁-C₆ alkoxycarbonyl, —NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, CF₃, C₁-C₆ alkanoyl, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkoxycarbonyl, halogen, C₃-C₆ cycloalkyl, OH, SH, or C₁-C₄ alkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A106. Compounds according to embodiment A105, wherein

• R₄ is H, alkyl substituted with one or two groups that are independently CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇.

Embodiment A112. Compounds according to embodiment 16, wherein

• R₁ is halogen, or methyl;
• R₂ is benzyloxy, which is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, CF₃, OCF₃, or (C₁-C₄)alkyl; and
• R₄ is H, methyl, ethyl, —CH₂OH, —CH₂CO₂—(C₁-C₄ alkyl), or C₂ hydroxyalkyl.

Embodiment A113. Compounds according to any one of embodiments A85, A95, A97, A98, A99, A100, 16 or 17, wherein

• R₁ is halogen, or methyl;
• R₂ is benzyloxy, which is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, CF₃, OCF₃, or (C₁-C₄)alkyl; and
• R₄ is alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇.

Embodiment A 114. Compounds according to embodiment A66, wherein

• R₅ is isoquinolinyl(C₁-C₆ alkyl), tetrahydroisoquinolinyl(C₁-C₆ alkyl), 1H-indazolyl(C₁-C₆ alkyl), dihydroindolonyl(C₁-C₆ alkyl), indolinyl(C₁-C₆ alkyl), dihydroisoindolyl(C₁-C₆ alkyl), dihydrobenzimdazolyl(C₁-C₆ alkyl), dihydrobenzoimidazolonyl(C₁-C₆ alkyl), each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently alkyl, alkoxy, halogen, C₁-C₆ alkoxycarbonyl, alkanoyl optionally substituted with 1 or 2 groups that are independently selected from the group consisting of OH, NH₂, NH(C₁-C₆ alkyl), and N(C₁-C₆ alkyl) (C₁-C₆ alkyl), —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, or SO₂H; or
• piperidinyl C₁-C₄ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, or —NR₆R₇, or C₁-C₆ alkoxycarbonyl.

Embodiment A115. Compounds according to embodiment A114, wherein

• R₅ is isoquinolinyl(C₁-C₄ alkyl), piperidinyl C₁-C₄ alkyl, tetrahydroisoquinolinyl(C₁-C₄ alkyl), 1H-indazolyl(C₁-C₄ alkyl), dihydroindolonyl(C₁-C₄ alkyl), indolinyl(C₁-C₄ alkyl), dihydroisoindolyl(C₁-C₄ alkyl), dihydrobenzimdazolyl(C₁-C₄ alkyl), or dihydrobenzoimidazolonyl(C₁-C₄ alkyl).

Embodiment A116. Compounds according to embodiment A114, wherein

• R₅ is piperidinyl C₁-C₄ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, or C₁-C₆ alkoxycarbonyl.

Embodiment A117. Compounds according to embodiment A66, wherein

• R₅ is pyrimidyl, indolinyl, indolyl, 1H-isoindolyl, isoquinolinyl, tetrahydroisoquinolinyl, benzimidazolyl, dihydro-1H-benzimidazolyl, pyrrolyl, imidazolyl, or each of which is optionally substituted with 1, 2, or 3 groups independently selected from the group consisting of
  • C₁-C₆ alkoxycarbonyl, C₁-C₄ thioalkoxy, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, alkyl, alkoxy, halogen, C₁-C₆ alkoxycarbonyl, or alkanoyl optionally substituted with 1 or 2 groups that are independently selected from the group consisting of OH, NH₂, NH(C₁-C₆ alkyl), and N(C₁-C₆ alkyl) (C₁-C₆ alkyl), and SO₂H; or
  • pyridyl, pyrazolyl, optionally substituted with 1, 2, or 3 groups that are independently —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, halogen, C₁-C₆ alkoxycarbonyl, —NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, CF₃, C₁-C₆ alkanoyl, wherein
    • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkoxycarbonyl, halogen, C₃-C₆ cycloalkyl, OH, SH, or C₁-C₄ alkoxy; or
    • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A118. Compounds according to embodiment A117, wherein

• R₅ is pyrimidyl, pyrrolyl, imidazolyl, or pyrazolyl, each of which is optionally substituted with 1, 2, or 3 groups independently selected from C₁-C₆ alkoxycarbonyl, C₁-C₄ thioalkoxy, each of which is unsubstituted or substituted with 1, 2, or 3 groups that are independently
  • alkyl, alkoxy, halogen, C₁-C₆ alkoxycarbonyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, or —NR₆R₇, or C₁-C₄ alkanoyl optionally substituted with 1 or 2 groups that are independently selected from the group consisting of OH, NH₂, NH(C₁-C₆ alkyl), and N(C₁-C₆ alkyl) (C₁-C₆ alkyl), or SO₂H.

Embodiment A119. Compounds according to embodiment A117, wherein

• R₅ is pyridyl or pyrazolyl, optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, or —NR₆R₇, C₁-C₆ alkoxycarbonyl, —NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, CF₃, C₁-C₆ alkanoyl, wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkoxycarbonyl, halogen, C₃-C₆ cycloalkyl, OH, SH, or C₁-C₄ alkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A120. Compounds according to embodiment A119, wherein

• R₅ is pyridyl or pyrazolyl, optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, C₁-C₆ alkoxycarbonyl, CF₃, C₁-C₆ alkanoyl, wherein
• R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkoxycarbonyl, halogen, C₃-C₆ cycloalkyl, OH, SH, or C₁-C₄ alkoxy.

Embodiment A121. Compounds according to embodiment A119, wherein

• R₅ is pyridyl or pyrazolyl, optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, halogen, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, C₁-C₆ alkoxycarbonyl, CF₃, C₁-C₆ alkanoyl, wherein
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A122. Compounds according to any one of embodiments A114, A115, A116, or A117 wherein

• R₁ is halogen, methyl, ethyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, or NR₆R₇—(C₁-C₆ alkyl)-; and
• R₄ is H, (C₁-C₄)alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, hydroxy(C₁-C₄)alkyl.

Embodiment A123. Compounds according to embodiment A66, wherein

• R₅ is C₁-C₆ alkyl optionally substituted with 1 or 2, groups that are independently C₁-C₄ alkoxycarbonyl, or halogen, or
• R₅ is C₁-C₄ alkoxy, ethyl, methyl, cyclopropylmethyl, cycloalkyl, or alkynyl, or R₅ is C₂-C₆ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl or cyclohexyl.

Embodiment A124. Compounds according to embodiment A123, wherein

• R₁ is halogen, methyl, ethyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₂ is benzyloxy, OH, phenyloxy, phenyloxy(C₁-C₆)alkyl, or phenyl(C₁-C₄)thioalkoxy, wherein each of the above is optionally substituted with 1, 2, 3, or 4 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, NR₆R₇, (C₁-C₄)haloalkyl, (C₁-C₄)haloalkoxy, (C₁-C₆)alkyl, pyridyl, or NR₆R₇—(C₁-C₆ alkyl)-; and
• R₄ is H, (C₁-C₄)alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, hydroxy(C₁-C₄)alkyl; wherein
  • R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkoxycarbonyl, halogen, C₃-C₆ cycloalkyl, OH, SH, or C₁-C₄ alkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a piperidinyl, pyrrolidinyl, piperazinyl, or a morpholinyl ring optionally substituted with 1 or 2 groups that are independently alkyl, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A125. Compounds according to embodiment A124, wherein

• R₅ is C₁-C₆ alkyl optionally substituted with 1 or 2, groups that are independently C₁-C₄ alkoxycarbonyl, or halogen, or
• R₅ is C₁-C₄ alkoxy, ethyl, methyl, cyclopropylmethyl, cyclohexyl, cyclopentyl, C₂-C₆ alkynyl, or
• R₅ is C₂-C₆ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl or cyclohexyl.

Embodiment A126. Compounds according to embodiment A66, wherein

• R₂ is phenylalkynyl, —OC(O)NH(CH₂)_naryl, —OC(O)N(alkyl)(CH₂)_naryl, —OSO₂(C₁-C₆)alkyl, —OSO₂aryl, or NR₈R₉, wherein
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, alkoxy, alkoxycarbonyl, CN, NR₆R₇, haloalkyl, haloalkoxy, alkyl, heteroaryl, heteroarylalkyl, NR₆R₇—(C₁-C₆ alkyl)-, phenyl, —SO₂-phenyl wherein the phenyl groups are optionally substituted with 1, 2, or 3 groups that are independently halogen or NO₂; or —OC(O)NR₆R₇, wherein
    • R₆ and R₇ are independently at each occurrence H, alkyl, alkoxy, alkoxyalkyl, alkoxycarbonyl, —SO₂-alkyl, OH, hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, heteroarylalkyl, alkanoyl, arylalkyl, arylalkoxy, or arylalkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, heterocycloalkyl, OH, NH₂, C₃-C₆ cycloalkyl, NH(alkyl), N(alkyl)(alkyl), —O-alkanoyl, alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
    • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A127. Compounds according to embodiment A126, wherein

• R₁ is halogen, methyl, ethyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, or carboxaldehyde; and
• R₄ is H, (C₁-C₄)alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, —NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, or hydroxy(C₁-C₄)alkyl.

Embodiment A128. Compounds according to embodiment A127, wherein

• R₅ is phenyl, optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, CF₃, OCF₃, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, or C(O)NR₆R₇, wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, C₃-C₆ cycloalkyl, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen; or
• R₅ is benzyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₆ alkyl, C₁-C₆ alkoxy, CN, CF₃, OCF₃, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, or C(O)NR₆R₇.

Embodiment A129. Compounds according to embodiment A128, wherein

• R₂ is NR₈R₉, or NR₈R₉—(C₁-C₄ alkyl)-; wherein
  • R₈ at each occurrence is independently hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl(C₁-C₆)alkyl or phenyl(C₁-C₆)alkanoyl wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxycarbonyl, halogen, or C₁-C₄ haloalkyl; and
  • R₉ at each occurrence is independently C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl(C₁-C₆)alkyl, C₃-C₇ cycloalkyl, C₂-C₆ alkenyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, imidazolyl, C₃-C₇ cycloalkyl(C₁-C₆)alkyl, phenyl(C₁-C₆)alkanoyl, —SO₂-phenyl, and phenyl wherein each of the above is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxycarbonyl, halogen, or C₁-C₄ haloalkyl.

Embodiment A130. Compounds according to embodiment A129, wherein R₈ is H.

Embodiment A131. Compounds according to embodiment A130, wherein

• R₂ is —NH-benzyl option substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, CF₃, OCF₃, or
• R₂ is —NH—C(O)phenyl, wherein the phenyl group is optionally substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkyl, or C₁-C₄ alkoxy; or
• R₂ is —NH-allyl.

Embodiment A132. Compounds according to embodiment A131, wherein

• R₁ is chloro, bromo, iodo, or methyl; and
• R₅ is benzyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, C₁-C₆ alkyl, C₁-C₆ alkoxy, CN, CF₃, OCF₃, or C(O)NR₆R₇.

Embodiment A133. Compounds according to embodiment A131, wherein

• R₁ is chloro, bromo, iodo, or methyl; and
• R₅ is phenyl, optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₄ alkyl)-C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —NR₆R₇, C₁-C₄ alkyl, C₁-C₄ alkoxy, CF₃, OCF₃, or C(O)NR₆R₇.

Embodiment A134. A compound of the formula or pharmaceutically acceptable salts thereof, wherein

• R₅ is wherein
• X₁, X₂, X_a, X_b, X_c, X_d, and X_e at are independently selected from —C(O)NR₆R₇, —NR₆R₇, hydroxy(C₁-C₄)alkyl, H, OH, halogen, haloalkyl, alkyl, haloalkoxy, heteroaryl, heterocycloalkyl, C₃-C₇ cycloalkyl, NR₆R₇—(C₁-C₆ alkyl)-, —CO₂—(C₁-C₆)alkyl, —N(R)C(O)NR₆R₇, —N(R)C(O)—(C₁-C₆)alkoxy, CO₂H—(C₁-C₆ alkyl)-, or —SO₂NR₆R₇; wherein
  • the heteroaryl and heterocycloalkyl groups are optionally substituted with —NR₆R₇, —C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, C₁-C₆ alkyl, C₁-C₆ alkoxy, or halogen;
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, C₁-C₆ thiohydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
  • R at each occurrence is independently H or C₁-C₆ alkyl; and
• Y, Y₁, Y₂, Y₃, and Y₄ are independently selected from H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, alkenyl, alkynyl, CN, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, and carboxyl.

Embodiment A135. Compounds according to embodiment A134, wherein

• Y₂, Y₄, and Y are independently halogen; and
• Y₁ and Y₃ are both hydrogen.

Embodiment A136. Compounds according to embodiment A135, wherein

• X₁ is H, methyl, —NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, C₁-C₆ hydroxyalkyl, or —(C₁-C₄ alkyl)-morpholinyl.

Embodiment A137. Compounds according to embodiment A136, wherein

• X_a and X_e are independently halogen, is NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl) or methyl.

Embodiment A138. Compounds according to embodiment A137, wherein

• X_b or X_c is —NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —SO₂NR₆R₇, or halogen; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A139. Compounds according to embodiment A138, wherein

• R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A140. Compounds according to embodiment A138, wherein

• R₆, R₇, and the nitrogen to which they are attached form a piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A141. Compounds according to embodiment A138, wherein

• R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O-C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃.

Embodiment A142. Compounds according to embodiment A138, wherein

• R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, or C₁-C₆ alkanoyl, wherein each of the above is optionally substituted with 1, 2, or 3 groups that are independently OH, SH, halogen, or C₃-C₆ cycloalkyl.

Embodiment A143. Compounds according to embodiment A137, wherein

• X_a and X_e are independently fluoro, chloro, or methyl; and
• X_c is hydrogen or halogen.

Embodiment A144. Compounds according to embodiment A137, wherein

• X_a is halogen;
• X_c is NH₂, NH(C₁-C₆ alkyl) or N(C₁-C₆ alkyl)(C₁-C₆ alkyl);
• X_b and X_d are both hydrogen.

Embodiment A145. Compounds according to embodiment A144, wherein

• X_c is —NR₆R₇, NR₆R₇ C₁-C₆ alkyl, —SO₂NR₆R₇, or halogen; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A146. Compounds according to embodiment A145, wherein

• X_c is fluoro, chloro, NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or piperazinyl, wherein the piperazinyl group is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A147. Compounds according to either embodiment A137 or A144, wherein

• X_c is —C(O)NR₆R₇, —(C₁-C₆ alkyl)-C(O)NR₆R₇, NR₆R₇, or NR₆R₇—(C₁-C₆ alkyl)-; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O-C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A148. Compounds according to embodiment A147, wherein

• R₆ is hydrogen; and
• R₇ is C₁-C₆ alkyl or C₁-C₆ alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), OH, SH, cyclopropyl, or C₁-C₄ alkoxy.

Embodiment A148a. Compounds according to embodiment A148, wherein

• R₇ is C₁-C₆ alkanoyl optionally substituted with 1, 2, or 3 groups that are independently OH, cyclopropyl, or NH₂.

Embodiment A149. Compounds according to embodiment A135, wherein

• X_a is hydrogen;
• X_b, X_c, or X_d is —C(O)NR₆R₇, —(C₁-C₆ alkyl)-C(O)NR₆R₇, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)- or —CO₂—(C₁-C₆)alkyl; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen; and
• X_e is hydrogen, methyl, C₁-C₂ alkoxy, or halogen.

Embodiment A150. Compounds according to embodiment A149, wherein

• X_b is NR₆R₇, or NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇ or —CO₂—(C₁-C₆)alkyl; wherein
• R₆ is hydrogen or C₁-C₄ alkyl;
• R₇ is OH, C₁-C₆ alkyl or C₁-C₆ alkanoyl, wherein the alkyl and alkanoyl groups substituted with 1, 2, or 3 groups that are independently NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₃-C₆ cycloalkyl, OH, or C₁-C₄ alkoxy.

Embodiment A151. Compounds according to embodiment A137, wherein

• X_a is halogen;
• X_b is NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, or —CO₂—(C₁-C₆)alkyl;
• X_c is NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, halogen, —CO₂—(C₁-C₆)alkyl, NH₂, NH(C₁-C₆ alkyl), N(C₁-C₆ alkyl)(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or piperazinyl, wherein the piperazinyl group is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
• X_d is hydrogen;
• X_e is H, methyl, NH₂, NH(C₁-C₆ alkyl) or N(C₁-C₆ alkyl)(C₁-C₆ alkyl).

Embodiment A152. Compounds according to embodiment A135, wherein

• X₁, X₂, X_a, X_b, X_c, X_d, and X_e are independently selected from H, OH, halogen, CF₃, alkyl, OCF₃, pyridyl, pyridazinyl, pyrimidyl, pyrazinyl, thienyl, furyl, pyrrolyl, piperidinyl, piperazinyl, or C₃-C₇ cycloalkyl, wherein each of the above is optionally substituted with —NR₆R₇, —C(O)NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, C₁-C₆ alkyl, C₁-C₆ alkoxy, or halogen.

Embodiment A153. Compounds according to embodiment A152, wherein at least three of X₁, X₂, X_a, X_b, X_c, X_d, and X_e are hydrogen.

Embodiment A154. A compound of the formula: or a pharmaceutically acceptable salt thereof, wherein

• R₁ is alkanoyl, halogen, arylalkanoyl, arylalkyl, alkoxyalkyl, hydroxyalkyl, or carboxaldehyde, wherein
  • the aryl portion of arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO₂H;
  • the alkyl portion of the hydroxyalkyl, arylalkyl, alkanoyl, alkoxyalkyl and arylalkanoyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, ethoxy or spirocyclopropyl;
• R₂ is arylalkoxy, aryloxy, phenyloxy(C₁-C₆)alkyl, OH, halogen, arylthioalkoxy, alkoxy, —OC(O)NH(CH₂)_naryl, —OC(O)N(alkyl)(CH₂)_naryl, alkyl, alkoxyalkoxy, dialkylamino, pyridyl, pyrimidyl, pyridazyl, pyrazolyl, imidazolyl, pyrrolyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, tetrazolyl, pyrazinyl, benzimidazolyl, triazinyl, tetrahydrofuryl, piperidinyl, hexahydropyrimidinyl, thiazolyl, thienyl, or CO₂H, wherein
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • the aryl portion of arylalkoxy, aryloxy, arylthioalkoxy, —OC(O)NH(CH₂)_naryl, and —OC(O)N(alkyl)(CH₂)_naryl or the heteroaryl and heterocycloalkyl groups is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, haloalkyl, heteroaryl, heteroarylalkyl, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —OC(O)NR₆R₇, wherein
    • R₆ and R₇ are independently at each occurrence H, alkyl, alkoxy, alkanoyl, arylalkyl, arylalkoxy, or arylalkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, SH, C₃-C₆ cycloalkyl, alkoxy, alkyl, haloalkyl, or haloalkoxy; or
    • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, alkoxycarbonyl, hydroxyl, hydroxyalkyl, or halogen;
    • R at each occurrence is independently H or C₁-C₆ alkyl;
    • R₃₀ is C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
• R₃ is halogen, arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylalkoxy, —OC(O)N(alkyl)(CH₂)_naryl, aryloxy, arylthio, thioalkoxy, arylthioalkoxy, alkenyl, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, or alkyl, wherein
  • the aryl portion of arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylalkoxy, —OC(O)N(alkyl)(CH₂)_naryl, and arylthioalkoxy, is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, alkyl, haloalkyl, or haloalkoxy,
    • wherein n is 0, 1, 2, 3, 4, 5, or 6; or
• R₄ is H, alkyl substituted with one group selected from CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, and —NR₆R₇, arylalkoxy, arylalkyl, hydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the aryl portion of arylalkoxy, arylalkyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, haloalkyl, or haloalkoxy; and
• R₅ is arylalkyl, alkyl, aryl, alkoxy, heterocycloalkylalkyl, heteroarylalkyl, arylthioalkyl, heterocycloalkyl, or heteroaryl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO₂H, CN, amidinooxime, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, haloalkyl, or haloalkoxy.

Embodiment A160. Compounds according to embodiment A154 wherein

• R₁ is halogen, (C₁-C₆)alkanoyl, phenyl(C₁-C₆)alkanoyl, naphthyl(C₁-C₆)alkanoyl, naphthyl(C₁-C₆)alkyl, phenyl(C₁-C₆)alkyl, alkoxyalkyl, hydroxyalkyl, or carboxaldehyde, wherein
  • the phenyl and naphthyl portions of the above are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, CF₃, OCF₃ or CO₂H;
  • the alkyl portion of the above groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy.
• R₂ is phenylalkoxy, aryloxy, phenyloxy(C₁-C₆)alkyl, OH, halogen, phenylthioalkoxy, alkoxy, alkyl, alkoxyalkoxy, —OC(O)NH(CH₂)_nphenyl, —OC(O)N(alkyl)(CH₂)_nphenyl, pyridyl, pyrimidyl, pyridazyl, pyrazolyl, or thienyl, wherein
  • n is 0, 1, 2, 3, or 4, and
  • the above groups are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, halo(C₁-C₄)alkyl, or thienyl;
• R₃ is halogen, phenylalkoxycarbonyl, phenyloxycarbonyl, phenyl(C₁-C₆)alkyl, phenylalkoxy, phenyloxy, phenylthio, thioalkoxy, arylthioalkoxy, (C₂-C₆)alkenyl, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, or alkyl, wherein
  • the phenyl, naphthyl, and aryl portions of arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylthioalkoxy, arylalkoxy, and —OC(O)N(alkyl)(CH₂)_naryl, are unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, alkyl, CF₃, or OCF₃,
• wherein n is 0, 1, 2, 3, 4, 5, or 6; or
• R₄ is H, (C₁-C₆)alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenylalkoxy, phenyl(C₁-C₆)alkyl, hydroxyalkyl, haloalkyl, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the phenyl portion of the above groups are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, CF₃, or OCF₃.
• R₅ is phenyl(C₁-C₆)alkyl, (C₁-C₆)alkyl, phenyl, naphthyl, pyridyl, (C₁-C₆)alkoxy, piperidinyl(C₁-C₆)alkyl, pyrrolyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, pyrazolyl(C₁-C₆)alkyl, imidazolyl(C₁-C₆)alkyl, tetrahydropyridinyl(C₁-C₆)alkyl, thienyl(C₁-C₆)alkyl, phenylthio(C₁-C₆)alkyl, or pyridyl(C₁-C₆)alkyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently (C₁-C₄)alkyl, fluoro, chloro, bromo, (C₁-C₄)alkoxy, phenyl(C₁-C₄)alkoxy, thio(C₁-C₄)alkoxy, (C₁-C₄)alkoxycarbonyl, phenyl(C₁-C₄)alkoxycarbonyl, CO₂H, CN, amidinooxime, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, CF₃, —CF₂CF₃, OCF₃ or OCF₂CF₃.

Embodiment A161. Compounds according to embodiment A160 wherein

• R₁ is halogen, (C₁-C₄)alkanoyl, phenyl(C₁-C₄)alkanoyl, benzyl, phenethyl, phenpropyl, hydroxyalkyl, or carboxaldehyde, wherein
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, CF₃, OCF₃ or CO₂H;
  • the alkyl portion of the above groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy;
• R₂ is benzyloxy, phenethyloxy, phenpropyloxy, phenbutyloxy, phenyloxy, phenyloxy(C₁-C₆)alkyl, OH, halogen, phenylthioalkoxy, alkoxy, alkyl, alkoxyalkoxy, wherein
  • n is 0, 1, 2, 3, or 4, and
  • the above groups are unsubstituted or substituted with 1, 2, or 3, groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, halo(C₁-C₄)alkyl, or thienyl;
• R₃ is halogen, phenylalkoxycarbonyl, phenyloxycarbonyl, phenyl(C₁-C₆)alkyl, phenylalkoxy, phenyloxy, phenylthio, thioalkoxy, phenylthioalkoxy, (C₂-C₆)alkenyl, NR₆R₇, NR₆R₇ C₁-C₆ alkyl, or alkyl, wherein
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, (C₁-C₄)alkyl, CF₃, or OCF₃,
• R₄ is H, (C₁-C₆)alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenylalkoxy, benzyl, phenethyl, hydroxyalkyl, haloalkyl, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the phenyl portion of the above groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, (C₁-C₄)alkoxy, (C₁-C₄)alkyl, nitro, CF₃, or OCF₃.
• R₅ is benzyl, phenethyl, phenpropyl, phenbutyl, (C₁-C₆)alkyl, phenyl, or pyridyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently (C₁-C₄)alkyl, fluoro, chloro, bromo, (C₁-C₄)alkoxy, phenyl(C₁-C₄)alkoxy, thio(C₁-C₄)alkoxy, (C₁-C₄)alkoxycarbonyl, CO₂H, CN, amidinooxime, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, CF₃, or OCF₃.

Embodiment A162. Compounds according to embodiment A161 wherein

• R₁ is bromo, phenyl(C₁-C₄)alkanoyl, benzyl, phenethyl, phenpropyl, hydroxyalkyl, or carboxaldehyde, wherein
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, CF₃, OCF₃ or CO₂H;
• R₂ is benzyloxy, phenethyloxy, phenpropyloxy, phenbutyloxy, phenyloxy, phenyloxy(C₁-C₆)alkyl, OH, halogen, or phenylthioalkoxy, wherein
  • n is 0, 1, 2, 3, or 4, and
  • the above groups are unsubstituted or substituted with 1, 2, or 3, groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, halo(C₁-C₄)alkyl, or thienyl;
• R₃ is bromo, phenylalkoxycarbonyl, phenyloxycarbonyl, phenyl(C₁-C₆)alkyl, phenylalkoxy, phenyloxy, phenylthio, thioalkoxy, phenylthioalkoxy, (C₂-C₆)alkenyl, NR₆R₇, NR₆R₇ C₁-C₆ alkyl, or alkyl, wherein
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, (C₁-C₄)alkyl, CF₃, or OCF₃,
• R₄ is H, (C₁-C₆)alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenylalkoxy, benzyl, or phenethyl, wherein
  • the phenyl portion of the above groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, (C₁-C₄)alkoxy, (C₁-C₄)alkyl, nitro, CF₃, or OCF₃.
• R₅ is benzyl, phenethyl, phenpropyl, (C₁-C₆)alkyl, phenyl, or pyridyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently (C₁-C₄)alkyl, fluoro, chloro, bromo, (C₁-C₄)alkoxy, CO₂H, CN, amidinooxime, amidino, CF₃, OCF₃, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, or —C(O)NR₆R₇; wherein
  • R₆ and R₇ are independently hydrogen, OH, C₁-C₄ alkoxy, C₁-C₆ alkanoyl, or C₁-C₆ alkyl, wherein each of the above is optionally substituted with 1 or 2 groups that are independently OH, NH₂, C₃-C₆ cycloalkyl, or halogen; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A163. Compounds of the formula or pharmaceutically acceptable salts thereof, wherein

• R₁ is H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, arylalkoxy, arylalkyl, CN, alkanoyl, alkoxy, alkoxyalkyl, or arylalkanoyl,
  • wherein the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO₂H;
  • wherein the alkyl portion of the alkyl, hydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl groups is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, ethoxy or spirocyclopropyl;
• R₂ is H, arylthio, —OC(O)NH(CH₂)_naryl, arylalkyl, —OC(O)N(alkyl)(CH₂)_naryl, or arylthioalkoxy, wherein n is 1, 2, 3, 4, or 5; wherein the aryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, C₁-C₄ alkoxy, C₁-C₄ alkyl, CF₃, or OCF₃;
  • R at each occurrence is independently H or C₁-C₆ alkyl;
  • R₃₀ is C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
• R₃ is halogen, alkoxycarbonyl, arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylalkoxy, —OC(O)N(alkyl)(CH₂)_naryl, aryloxy, arylthio, thioalkoxy, arylthioalkoxy, alkenyl, NR₆R₇ C₁-C₆ alkyl, NR₆R₇ or alkyl, wherein
  • the aryl portion of arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylalkoxy, —OC(O)N(alkyl)(CH₂)_naryl, and arylthioalkoxy, is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, alkyl, haloalkyl, or haloalkoxy,
    • wherein n is 0, 1, 2, 3, 4, 5, or 6; or
• R₄ is H, alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, arylalkoxy, arylalkyl, hydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the aryl portion of arylalkoxy, arylalkyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, haloalkyl, or haloalkoxy; and
• R₅ is arylalkyl, alkyl, aryl, alkoxy, heterocycloalkylalkyl, heteroarylalkyl, arylthioalkyl, heterocycloalkyl, or heteroaryl, wherein each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO₂H, CN, amidinooxime, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, haloalkyl, or haloalkoxy; wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A168. Compounds according to embodiment A163 wherein

• R₅ is benzyl, phenethyl, phenpropyl, phenbutyl, alkyl, phenyl, alkoxy, pyridyl(C₁-C₆)alkyl, phenyl(C₁-C₆)thioalkyl, pyrrolyl, pyrrolyl(C₁-C₆)alkyl, or pyridyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently (C₁-C₆)alkyl, halogen, (C₁-C₆)alkoxy, phenyl(C₁-C₆)alkoxy, (C₁-C₆)thioalkoxy, alkoxycarbonyl, CO₂H, CN, amidinooxime, amidino, CF₃, or OCF₃.

Embodiment A169. Compounds according to embodiment A163 wherein

• R₁ is H, Cl, Br, (C₁-C₆)alkyl, carboxaldehyde, hydroxy(C₁-C₆)alkyl,
  • wherein the alkyl portion of above is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy
• R₂ is H, phenylthio, —OC(O)NH(CH₂)_naryl, phenylalkyl, —OC(O)N(alkyl)(CH₂)_naryl, or phenylthio(C₁-C₆)alkoxy, wherein n is 1, 2, 3, or 4;
  • wherein the aryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, C₁-C₄ alkoxy, C₁-C₄ alkyl, CF₃, or OCF₃;
• R₃ is bromo, alkoxycarbonyl, phenylalkoxycarbonyl, phenyloxycarbonyl, phenylalkyl, phenylalkoxy, phenyloxy, phenylthio, thioalkoxy, phenylthioalkoxy, alkenyl, NR₆R₇ or alkyl, wherein
  • the phenyl portion of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, (C₁-C₄)alkoxy, (C₁-C₄)alkyl, halo(C₁-C₄)alkyl, or halo(C₁-C₄)alkoxy,
  • wherein n is 0, 1, 2, 3, or 4;
• R₄ is H, alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenylalkoxy, phenylalkyl, hydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or wherein
  • the phenyl portion of phenylalkoxy, phenylalkyl is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, haloalkyl, or haloalkoxy
• R₅ is benzyl, phenethyl, phenpropyl, phenbutyl, alkyl, phenyl, phenyl(C₁-C₆)thioalkyl, pyrrolyl, or pyridyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently (C₁-C₆)alkyl, halogen, (C₁-C₆)alkoxy, benzyloxy, (C₁-C₆)thioalkoxy, alkoxycarbonyl, CO₂H, CN, amidinooxime, amidino, CF₃, or OCF₃;
  • R₆ and R₇ are independently hydrogen, OH, C₁-C₄ alkoxy, C₁-C₆ alkanoyl, or C₁-C₆ alkyl, wherein each of the above is optionally substituted with 1 or 2 groups that are independently OH, NH₂, C₃-C₆ cycloalkyl, or halogen; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen.

Embodiment A170. Compounds according to embodiment 1 or a pharmaceutically acceptable salt thereof, wherein

• R₁ is H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, arylalkoxy, arylalkyl, CN, alkanoyl, alkoxy, alkoxyalkyl, or arylalkanoyl,
  • wherein the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO₂H;
  • wherein the alkyl portion of the alkyl, hydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl groups is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, ethoxy or spirocyclopropyl;
• R₂ is arylalkoxy, aryloxy, aryloxyalkyl, OH, halogen, arylthioalkoxy, alkoxy, —OC(O)NH(CH₂)_naryl, —OC(O)N(alkyl)(CH₂)_naryl, alkyl, alkoxyalkoxy, dialkylamino, or CO₂H, wherein
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • the aryl portion of arylalkoxy, aryloxy, arylthioalkoxy, —OC(O)NH(CH₂)_naryl, and —OC(O)N(alkyl)(CH₂)_naryl or the heteroaryl and heterocycloalkyl groups is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, haloalkyl, heteroaryl, heteroarylalkyl, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —OC(O)NR₆R₇, wherein
  • R₆ and R₇ are independently at each occurrence H, C₁-C₆ alkyl, C₁-C₆ alkoxy, C₁-C₆ alkoxy C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, OH, C₁-C₆ hydroxyalkyl, —(C₁-C₄)alkyl-CO₂-alkyl, pyridyl C₁-C₆ alkyl, C₁-C₆ alkanoyl, benzyl, phenyl C₁-C₆ alkoxy, or phenyl C₁-C₆ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, C₁-C₆ alkoxy, piperidinyl C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, piperazinyl C₁-C₆ alkyl, OH, SH, NH₂, NH(alkyl), N(alkyl)(alkyl), —O—C₁-C₄ alkanoyl, C₁-C₄ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, hydroxy, hydroxy C₁-C₄ alkyl, or halogen;
  • R at each occurrence is independently H or C₁-C₆ alkyl;
  • R₃₀ is C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
• R₃ is halogen, alkoxycarbonyl, arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylalkoxy, —OC(O)N(alkyl)(CH₂)_naryl, aryloxy, arylthio, thioalkoxy, arylthioalkoxy, alkenyl, NR₆R₇ C₁-C₆ alkyl, NR₆R₇ or alkyl, wherein
  • the aryl portion of arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH₂)_naryl, arylalkoxy, —OC(O)N(alkyl)(CH₂)_naryl, and arylthioalkoxy, is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, alkyl, haloalkyl, or haloalkoxy,
    • wherein n is 0, 1, 2, 3, 4, 5, or 6; or
• R₄ is H, alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, arylalkoxy, arylalkyl, hydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the aryl portion of arylalkoxy, arylalkyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, haloalkyl, or haloalkoxy; and
• R₅ is aryl, heterocycloalkylalkyl, heteroarylalkyl, arylthioalkyl, heterocycloalkyl, or heteroaryl, wherein each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently alkyl, halogen, alkoxy, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO₂H, CN, amidinooxime, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, haloalkyl, or haloalkoxy.

Embodiment A173. Compounds according to embodiment A170 wherein

• R₁ is H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, benzyloxy, phenethyloxy, phenpropyloxy, benzyl, phenethyl, phenpropyl, CN, alkanoyl, alkoxy, or phenylC(O)—, phenylCH₂C(O)—, or phenylCH₂CH₂C(O),
  • wherein the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, CF₃, OCF₃ or CO₂H;
  • wherein the above alkyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, methoxy, or ethoxy;
• R₂ is benzyloxy, phenethyloxy, phenpropyloxy, phenyloxy, phenyloxy(C₁-C₆)alkyl, OH, halogen, phenylthioalkoxy, alkyl, alkoxy, —OC(O)NH(CH₂)_nphenyl, —OC(O)N(alkyl)(CH₂)_nphenyl, dialkylamino, or CO₂H, wherein
  • n is 0, 1, 2, 3, or 4;
  • the above aryl groups are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, CF₃, pyridyl, thienyl, NR₆R₇, or NR₆R₇—(C₁-C₆ alkyl)-, wherein
    • R₆ and R₇ are independently at each occurrence H, alkyl, alkanoyl, benzyl, or phenylC(O)—, wherein the phenyl portion of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, C₃-C₆ cycloalkyl, alkoxy, alkyl, CF₃, or OCF₃;
• R₃ is halogen, alkoxycarbonyl, phenylalkoxycarbonyl, phenyloxycarbonyl, phenylalkyl, —OC(O)NH(CH₂)_nphenyl, phenylalkoxy, —OC(O)N(alkyl)(CH₂)_nphenyl, phenyloxy, phenylthio, thioalkoxy, phenylthioalkoxy, alkenyl, NR₆R₇ or alkyl, wherein
  • the phenyl portion of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, alkyl, haloalkyl, or haloalkoxy,
    • wherein n is 0, 1, 2, 3, or 4;
• R₄ is H, alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenylalkoxy, phenylalkyl, hydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the phenyl portion of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, haloalkyl, or haloalkoxy; and
• R₅ is phenyl, naphthyl, pyrrolylalkyl, piperidinylalkyl pyridinylalkyl, pyrimidinylalkyl, phenylthioalkyl, pyrrolyl, piperidinyl, pyridyl, or thienylalkyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently alkyl, halogen, alkoxy, phenylalkoxy, thioalkoxy, alkoxycarbonyl, phenylalkoxycarbonyl, CO₂H, CN, amidinooxime, NR₆R₇, NR₆R₇—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, amidino, haloalkyl, or haloalkoxy.

Embodiment A174. Compounds according to embodiment A173 wherein

• R₁ is H, halogen, alkyl, carboxaldehyde, hydroxyalkyl, benzyloxy, phenethyloxy, benzyl, phenethyl, CN, (C₁-C₆)alkanoyl, alkoxy, or phenylC(O)—, or phenylCH₂C(O)—,
  • wherein the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy, nitro, CN, CF₃, OCF₃ or CO₂H;
• R₂ is benzyloxy, phenethyloxy, phenpropyloxy, phenyloxy, phenyloxy(C₁-C₆)alkyl, halogen, phenyl(C₁-C₄)thioalkoxy, —OC(O)NH(CH₂)_nphenyl, —OC(O)N(alkyl)(CH₂)_nphenyl, or dialkylamino, wherein
  • n is 0, 1, 2, 3, or 4;
  • the above phenyl groups are unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, CF₃, NR₆R₇, or NR₆R₇—(C₁-C₆ alkyl)-, wherein
    • R₆ and R₇ are independently at each occurrence H, (C₁-C₆)alkyl, acetyl, benzyl, or phenylC(O)—, wherein the phenyl portion of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, OH, cyclopropyl, alkoxy, alkyl, CF₃, or OCF₃;
• R₃ is halogen, alkoxycarbonyl, phenylalkoxycarbonyl, phenyloxycarbonyl, phenylalkyl, phenylalkoxy, phenyloxy, phenylthio, thioalkoxy, phenylthioalkoxy, alkenyl, NR₆R₇ or alkyl, wherein
  • the phenyl portion of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, alkoxy, alkyl, haloalkyl, or haloalkoxy,
    • wherein n is 0, 1, 2, 3, or 4;
• R₄ is H, alkyl substituted with one group that is CO₂H, —CO₂—(C₁-C₆)alkyl, —C(O)NRR, —N(R₃₀)C(O)NRR, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, phenylalkoxy, phenylalkyl, hydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the phenyl portion of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, haloalkyl, or haloalkoxy; and
• R₅ is phenyl, phenyl(C₁-C₄)thioalkyl, pyridyl, or thienyl(C₁-C₄)alkyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently (C₁-C₄)alkyl, fluoro, chloro, bromo, (C₁-C₄)alkoxy, CN, amidinooxime, amidino, CF₃, or OCF₃.

Embodiment A175. Compounds according to embodiment A174 wherein

• R₅ is substituted with at least one group selected from fluoro, chloro, bromo, and methyl.

In another aspect, the invention provides pharmaceutical compositions comprising at least one pharmaceutically acceptable carrier, solvent, adjuvant or excipient and a compound of formula I, embodiment A66, or embodiment A154.

The invention further provides pharmaceutical compositions comprising at least one pharmaceutically acceptable carrier, solvent, adjuvant or excipient and compounds according to any of the preceding embodiments.

As noted above, the invention encompasses methods of treating a TNF mediated disorder, a p38 kinase mediated disorder, inflammation and/or arthritis in a subject, the method comprising treating a subject having or susceptible to such disorder or condition with a therapeutically-effective amount of a compound of formula I or embodiment A1.

More specifically, the invention provides methods for treating or preventing inflammation; arthritis, rheumatoid arthritis, spondylarthropathies, gouty arthritis, osteoarthritis, systemic lupus erthematosus, juvenile arthritis, and other arthritic conditions; neuroinflammation; allergy, Th2 mediated diseases; pain, neuropathic pain; fever; pulmonary disorders, lung inflammation, adult respiratory distress syndrome, pulmonary sarcoisosis, asthma, silicosis, chronic pulmonary inflammatory disease, and chronic obstructive pulmonary disease (COPD); cardiovascular disease, arteriosclerosis, myocardial infarction (including post-myocardial infarction indications), thrombosis, congestive heart failure, cardiac reperfusion injury, as well as complications associated with hypertension and/or heart failure such as vascular organ damage, restenosis; cardiomyopathy; stroke including ischemic and hemorrhagic stroke; reperfusion injury; renal reperfusion injury; ischemia including stroke and brain ischemia, and ischemia resulting from cardiac/coronary bypass; neurotrauma and brain trauma including closed head injury; brain edema; neurodegenerative disorders; liver disease and nephritis; gastrointestinal conditions, inflammatory bowel disease, Crohn's disease, gastritis, irritable bowel syndrome, ulcerative colitis; ulcerative diseases, gastric ulcers; ophthalmic diseases, retinitis, retinopathies, uveitis, ocular photophobia, acute injury to the eye tissue and ocular traumas such as post-traumatic glaucoma, traumatic optic neuropathy, and central retinal artery occlusion (CRAO); periodontal disease; ophthalmological conditions, retinitis, retinopathies (including diabetic retinopathy), uveitis, ocular photophobia, nonglaucomatous optic nerve atrophy, and age related macular degeneration (ARMD) (including ARMD-atrophic form), corneal graft rejection, ocular neovascularization, retinal neovascularization, neovascularization following injury or infection, retrolental fibroplasias, neovascular glaucoma; glaucoma including primary open angle glaucoma (POAG), juvenile onset primary open-angle glaucoma, angle-closure glaucoma, pseudoexfoliative glaucoma, anterior ischemic optic neuropathy (AION), ocular hypertension, Reiger's syndrome, normal tension glaucoma, neovascular glaucoma, ocular inflammation and corticosteroid-induced glaucoma; diabetes; diabetic nephropathy; skin-related conditions, psoriasis, eczema, burns, dermatitis, keloid formation, scar tissue formation, angiogenic disorders; viral and bacterial infections, sepsis, septic shock, gram negative sepsis, malaria, meningitis, HIV infection, opportunistic infections, cachexia secondary to infection or malignancy, cachexia secondary to acquired immune deficiency syndrome (AIDS), AIDS, ARC (AIDS related complex), pneumonia, herpes virus; myalgias due to infection; influenza; endotoxic shock; toxic shock syndrome; autoimmune disease, graft vs. host reaction and allograft rejections; treatment of bone resorption diseases, osteoporosis; multiple sclerosis; disorders of the female reproductive system, endometriosis; hemaginomas, infantile hemagionmas, angiofibroma of the nasopharynx, avascular necrosis of bone; benign and malignant tumors/neoplasia, cancer, colorectal cancer, brain cancer, bone cancer, epithelial call-derived neoplasia (epithelial carcinoma), basal cell carcinoma, adenocarcinoma, gastrointestinal cancer, lip cancer, mouth cancer, esophageal cancer, small bowel cancer, stomach cancer, colon cancer, liver cancer, bladder cancer, pancreas cancer, ovarian cancer, cervical cancer, lung cancer, breast cancer, skin cancer, squamus cell and/or basal cell cancers, prostate cancer, renal cell carcinoma, and other known cancers that affect epithelial cells throughout the body; leukemia; lymphoma; systemic lupus erthrematosis (SLE); angiogenesis including neoplasia; metastasis; central nervous system disorders, central nervous system disorders having an inflammatory or apoptotic component, Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, spinal cord injury, and peripheral neuropathy; Canine B-Cell Lymphoma. Compounds of the invention are also useful for preventing the production or expression of cyclooxygenase-2, or cyclooxygenase-2 activity.

In this aspect, the invention encompasses methods of treating a p38 kinase or TNF-alpha mediated disorder comprising administering to a patient in need thereof a therapeutically effective amount of Compounds according to embodiment 1 and at least one pharmaceutically acceptable carrier, adjuvant, solvent or excipient.

Representative compounds of the invention are:

• 1-benzyl-4-(benzyloxy)-3-bromopyridin-2(1H)-one;
• 3-bromo-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-dimethylphenyl)-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 4-bromo-2-(2,6-dichlorophenyl)-5-[(2,4-difluorobenzyl)oxy]pyridazin-3(2H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(3-methylbenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-bromo-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-methoxy-6-methylphenyl)-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-methylbenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-chlorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(3-methoxybenzyl)pyridin-2(1H)-one;
• 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzoic acid;
• 4-(benzyloxy)-3-bromo-1-(2-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-1-(2,6-dimethylphenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[4-(methylthio)benzyl]pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-chloropyridin-2(1H)-one;
• 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}-N′-hydroxybenzenecarboximidamide;
• methyl 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• 3-bromo-4-[(3-chlorobenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 4-(benzyloxy)-3-bromo-1-(2,6-dichlorophenyl)-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-bromobenzyl)pyridin-2(1H)-one;
• 4-{[3-bromo-4-[(4-fluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]-3-iodopyridin-2(1H)-one;
• 4-bromo-2-(2,6-dichlorophenyl)-5-{[2-(hydroxymethyl)benzyl]oxy}pyridazin-3(2H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-1-(2,4-difluorobenzyl)-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-2-ylmethyl)pyridin-2(1H)-one; or a pharmaceutically acceptable salt thereof.

Embodiment 57. Compounds according to embodiment 1 or embodiment A1, which is

• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-(4-fluorobenzyl)pyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(4-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(4-chlorobenzyl)-4-[(4-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-[2-(phenylthio)ethyl]pyridin-2(1H)-one;
• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-(2-phenylethyl)pyridin-2(1H)-one;
• 3-bromo-4-hydroxy-1-(4-hydroxybenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(piperidin-3-ylmethyl)pyridin-2(1H)-one hydrochloride;
• 3-bromo-1-(4-methoxybenzyl)-4-phenoxypyridin-2(1H)-one;
• 1-benzyl-2-oxo-4-phenoxy-1,2-dihydropyridine-3-carbaldehyde;
• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-(4-methoxybenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(3-phenylpropyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-1-[4-(benzyloxy)benzyl]-3-bromopyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[2-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[3-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(piperidin-4-ylmethyl)pyridin-2(1H)-one hydrochloride;
• 1-benzyl-3-bromo-4-{[2-(trifluoromethyl)benzyl]oxy}pyridin-2(1H)-one;
• 1-benzyl-4-[(2,6-dichlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-(hydroxymethyl)pyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(2,6-dichlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(2-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-ethylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-(4-bromobenzyl)pyridin-2(1H)-one;
• 3-bromo-1-(4-methylbenzyl)-4-[(4-methylbenzyl)oxy]pyridin-2(1H)-one;
• methyl 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• 4-(benzyloxy)-3-bromo-1-(2-thien-3-ylethyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(2-thien-2-ylethyl)pyridin-2(1H)-one;
• 1-benzyl-4-[(3-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-1-(2-fluorobenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-methylpyridin-2(1H)-one hydrobromide;
• 4-(benzyloxy)-3-bromo-1-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-chlorobenzyl)-4-[(4-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(3-chlorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-(benzyloxy)-1-(4-chlorobenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethoxy)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-tert-butylbenzyl)pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-6-methylpyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3,5-dibromo-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 1-benzyl-4-[(2-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-(2-bromobenzyl)-3-[(2-bromobenzyl)oxy]pyridin-2(1H)-one;
• methyl 5-chloro-1-(4-chlorobenzyl)-6-oxo-1,6-dihydropyridine-3-carboxylate;
• 3-benzyl-4-hydroxy-1-(2-phenylethyl)pyridin-2(1H)-one;
• 5-bromo-1-(2-chloro-6-fluorobenzyl)-3-methylpyridin-2(1H)-one;
• 1-(2-bromobenzyl)-3-[(2-bromobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-bromopyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-2-oxo-1,2-dihydropyridine-3-carbaldehyde;
• 1-benzyl-4-chloro-2-oxo-1,2-dihydropyridine-3-carbaldehyde;
• 1-benzyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carbaldehyde;
• 1-benzyl-4-(benzyloxy)-3-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-(4-fluorobenzyl)pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3,5-dibromopyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[4-(methylthio)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-fluorobenzyl)pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-chloropyridin-2(1H)-one;
• 3-bromo-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate;
• 1-benzyl-3-bromo-4-(2-phenylethyl)pyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-(3-phenylpropyl)pyridin-2(1H)-one;
• 1-benzyl-3-methyl-4-(2-phenylethyl)pyridin-2(1H)-one;
• 1-benzyl-3-methyl-4-(3-phenylpropyl)pyridin-2(1H)-one;
• 1-benzyl-4-(benzylthio)-3-methylpyridin-2(1H)-one;
• 1-benzyl-4-(benzylthio)-3-bromopyridin-2(1H)-one;
• 1-benzyl-2-oxo-1,2-dihydropyridin-4-yl methanesulfonate;
• 3-acetyl-4-hydroxy-6-methyl-1-[choro]phenylpyridin-2(1H)-one;
• 6-(benzyloxy)-1-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile;
• 3-benzoyl-6-(benzyloxy)-1-methylpyridin-2(1H)-one;
• 3-benzyl-6-(benzyloxy)-1-methylpyridin-2(1H)-one;
• 1-benzyl-4-hydroxypyridin-2(1H)-one;
• 1-benzyl-4-(benzylthio)pyridin-2(1H)-one
• 4-amino-1-benzylpyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)pyridin-2(1H)-one;
• 1-benzyl-4-hydroxypyridin-2(11)-one;
• 1-benzyl-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate; or a pharmaceutically acceptable thereof.

Embodiment 58. Compounds according to embodiment 1 or embodiment A1, which is

• 4-(benzyloxy)-1-(4-methylbenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromopyridin-2(1H)-one;
• methyl 4-{[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• methyl-4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• 4-{[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 4-(benzyloxy)-1-(4-tert-butylbenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-1-[4-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[3-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[2-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-1-[4-(trifluoromethoxy)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethoxy)benzyl]pyridin-2(1H)-one;
• 1-benzyl-4-hydroxy-6-methylpyridin-2(1H)-one;
• 1-benzyl-6-methyl-2-oxo-1,2-dihydropyridin-4-yl 4-bromobenzenesulfonate;
• 1-benzyl-3-bromo-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-benzyl-6-methyl-2-oxo-1,2-dihydropyridin-4-yl 4-bromobenzenesulfonate;
• 1-benzyl-3-bromo-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-Benzyl-4-[2,6-(dichlorobenzyl)oxy]pyridin-2(1H)-one;
• 4-[(2,6-dichlororbenzyl)oxy]pyridine-1-oxide;
• 4-[(2,6-dichlorobenzyl)oxy]pyridine 1-oxide;
• 1-Benzyl-3-bromo-4-[2,6-(dichlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-Benzyl-3-bromo-4-[(4-methylbenzyl)oxy]pyridin-2(1H)-one;
• 1-Benzyl-4-[benzylthio]-3-bromopyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-iodopyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-vinylpyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-ethylpyridin-2(1H)-one;
• 3-acetyl-4-(benzyloxy)-1-(2-chlorophenyl)-6-methylpyridin-2(1H)-one;
• 3-acetyl-1-(2-chlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-hydroxypyridin-2(1H)-one;
• 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate;
• 1-benzyl-3-bromo-4-(phenylethynyl)pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(2-phenylethyl)pyridin-2(1H)-one;
• 1-(3-fluorobenzyl)-4-hydroxy-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-hydroxy-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate;
• 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(phenylethynyl)pyridin-2(1H)-one;
• 3-acetyl-1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one;
• 1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-(2,6-dichlorophenyl)-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-(2-phenylethyl)pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate;
• 3-bromo-1-(3-fluorobenzyl)-4-(phenylethynyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-ethynyl-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one;
• 4-(benzyloxy)-1-(3-fluorobenzyl)-3-[(trimethylsilyl)ethynyl]pyridin-2(1H)-one;
• 4-(benzylamino)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one;
• 4-(benzylamino)-1-(3-fluorobenzyl)pyridin-2(1H)-one;
  • or a pharmaceutically acceptable salt thereof.

Embodiment 59. Compounds according to embodiment 1 or embodiment A1, which is

• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(3-methoxybenzyl)pyridin-2(1H)-one;
• 3-bromo-1-(2,6-dimethylphenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(3-chlorobenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-{[3-bromo-4-[(4-fluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]-3-iodopyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-1-(2,4-difluorobenzyl)-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-2-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(3-methylbenzyl)oxy]piperidin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-methoxy-6-methylphenyl)-6-methylpyridin-2(1H)-one;
  • or a pharmaceutically acceptable salt thereof.

Embodiment 60. A Compound according to embodiment 1, which is

• 1-(1-acetyl-2,3-dihydro-1H-indol-5-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1-glycoloyl-2,3-dihydro-1H-indol-5-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-indol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(N-methylglycyl)-2,3-dihydro-1H-indol-5-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxypropanoyl)-2,3-dihydro-1H-indol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-indol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]indoline-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(methylsulfonyl)-2,3-dihydro-1H-indol-5-yl]pyridin-2(1H)-one;
• 1-(1-acetyl-1H-indol-5-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1-glycoloyl-1H-indol-5-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-1H-indol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(N-methylglycyl)-1H-indol-5-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxypropanoyl)-1H-indol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-1H-indol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-1H-indole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(methylsulfonyl)-1H-indol-5-yl]pyridin-2(1H)-one;
• 1-(2-acetyl-2,3-dihydro-1H-isoindol-5-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2-glycoloyl-2,3-dihydro-1H-isoindol-5-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-isoindol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(N-methylglycyl)-2,3-dihydro-1H-isoindol-5-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(3-hydroxypropanoyl)-2,3-dihydro-1H-isoindol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-isoindol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-1,3-dihydro-2H-isoindole-2-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(methylsulfonyl)-2,3-dihydro-1H-isoindol-5-yl]pyridin-2(1H)-one;
• 1-(2-acetyl-1,2,3,4-tetrahydroisoquinolin-6-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2-glycoloyl-1,2,3,4-tetrahydroisoquinolin-6-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(2-hydroxy-2-methylpropanoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(N-methylglycyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(3-hydroxypropanoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(3-hydroxy-3-methylbutanoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]-6-methylpyridin-2(1H)-one;
• 6-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,4-dihydroisoquinoline-2(1H)-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]pyridin-2(1H)-one;
• 1-(2-acetyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2-glycoloyl-1,2,3,4-tetrahydroisoquinolin-7-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(2-hydroxy-2-methylpropanoyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(N-methylglycyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(3-hydroxypropanoyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2-(3-hydroxy-3-methylbutanoyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]-6-methylpyridin-2(1H)-one;
• 7-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,4-dihydroisoquinoline-2(1H)-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridin-2(1H)-one;
• 1-(1-acetyl-1H-benzimidazol-5-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1-glycoloyl-1H-benzimidazol-5-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(N-methylglycyl)-1H-benzimidazol-5-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxypropanoyl)-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(methylsulfonyl)-1H-benzimidazol-5-yl]pyridin-2(1H)-one;
• 3-chloro-1-(1,3-diacetyl-2,3-dihydro-1H-benzimidazol-5-yl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-(3-acetyl-1-glycoloyl-2,3-dihydro-1H-benzimidazol-5-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-[3-acetyl-1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-[3-acetyl-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-[3-acetyl-1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-[3-acetyl-1-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-acetyl-5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 1-(1-acetyl-3-glycoloyl-2,3-dihydro-1H-benzimidazol-5-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1,3-diglycoloyl-2,3-dihydro-1H-benzimidazol-5-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-glycoloyl-1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-glycoloyl-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-glycoloyl-1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-glycoloyl-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-glycoloyl-1-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-glycoloyl-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 1-[1-acetyl-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-glycoloyl-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 1-[1,3-bis(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(2-hydroxy-2-methylpropanoyl)-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(2-hydroxy-2-methylpropanoyl)-1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(2-hydroxy-2-methylpropanoyl)-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 1-[1-acetyl-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-glycoloyl-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 1-[1,3-bis(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxypropanoyl)-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[3-(N-methylglycyl)-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]pyridin-2(1H)-one;
• 1-[1-acetyl-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-glycoloyl-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(3-hydroxypropanoyl)-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 1-[1,3-bis(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(3-hydroxypropanoyl)-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 1-[1-acetyl-3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-glycoloyl-3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(3-hydroxy-3-methylbutanoyl)-1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(3-hydroxy-3-methylbutanoyl)-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(3-hydroxy-3-methylbutanoyl)-1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 1-[1,3-bis(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(3-hydroxy-3-methylbutanoyl)-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-acetyl-6-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-glycoloyl-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-1H-benzimidazole-1,3(2H)-dicarboxamide;
• 6-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 1-[1-acetyl-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-glycoloyl-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(N-methylglycyl)-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxypropanoyl)-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-6-methylpyridin-2(1H)-one;
• 5-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 1-[1,3-bis(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-[3-acetyl-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-(1-acetyl-1H-pyrrol-3-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1-glycoloyl-1H-pyrrol-3-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-1H-pyrrol-3-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(N-methylglycyl)-1H-pyrrol-3-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxypropanoyl)-1H-pyrrol-3-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-1H-pyrrol-3-yl]-6-methylpyridin-2(1H)-one;
• 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-1H-pyrrole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(methylsulfonyl)-1H-pyrrol-3-yl]pyridin-2(1H)-one;
• 1-(1-acetyl-1H-imidazol-4-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1-glycoloyl-1H-imidazol-4-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-1H-imidazol-4-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(N-methylglycyl)-1H-imidazol-4-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxypropanoyl)-1H-imidazol-4-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-1H-imidazol-4-yl]-6-methylpyridin-2(1H)-one;
• 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-1H-imidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(methylsulfonyl)-1H-imidazol-4-yl]pyridin-2(1H)-one;
• 1-(1-acetyl-1H-pyrazol-4-yl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1-glycoloyl-1H-pyrazol-4-yl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(2-hydroxy-2-methylpropanoyl)-1H-pyrazol-4-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(N-methylglycyl)-1H-pyrazol-4-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxypropanoyl)-1H-pyrazol-4-yl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[1-(3-hydroxy-3-methylbutanoyl)-1H-pyrazol-4-yl]-6-methylpyridin-2(1H)-one;
• 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-1H-pyrazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[1-(methylsulfonyl)-1H-pyrazol-4-yl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-isoquinolin-7-yl-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(isoquinolin-6-ylmethyl)pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-indol-2-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,3-dihydro-1H-indol-5-ylmethyl)pyridin-2(1H)-one;
• 1-[(1-acetyl-2,3-dihydro-1H-indol-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(1-glycoloyl-2,3-dihydro-1H-indol-5-yl)methyl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(N-methylglycyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxypropanoyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}indoline-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(methylsulfonyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,3-dihydro-1H-isoindol-5-ylmethyl)pyridin-2(1H)-one;
• 1-[(2-acetyl-2,3-dihydro-1H-isoindol-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(2-glycoloyl-2,3-dihydro-1H-isoindol-5-yl)methyl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-isoindol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(N-methylglycyl)-2,3-dihydro-1H-isoindol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(3-hydroxypropanoyl)-2,3-dihydro-1H-isoindol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-isoindol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-isoindole-2-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(methylsulfonyl)-2,3-dihydro-1H-isoindol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1,2,3,4-tetrahydroisoquinolin-6-ylmethyl)pyridin-2(1H)-one;
• 1-[(2-acetyl-1,2,3,4-tetrahydroisoquinolin-6-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(2-glycoloyl-1,2,3,4-tetrahydroisoquinolin-6-yl)methyl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(2-hydroxy-2-methylpropanoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(N-methylglycyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(3-hydroxypropanoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(3-hydroxy-3-methylbutanoyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]methyl}pyridin-2(1H)-one;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3,4-dihydroisoquinoline-2(1H)-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinolin-6-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1,2,3,4-tetrahydroisoquinolin-5-ylmethyl)pyridin-2(1H)-one;
• 1-[(2-acetyl-1,2,3,4-tetrahydroisoquinolin-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(2-glycoloyl-1,2,3,4-tetrahydroisoquinolin-5-yl)methyl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(2-hydroxy-2-methylpropanoyl)-1,2,3,4-tetrahydroisoquinolin-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(N-methylglycyl)-1,2,3,4-tetrahydroisoquinolin-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(3-hydroxypropanoyl)-1,2,3,4-tetrahydroisoquinolin-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(3-hydroxy-3-methylbutanoyl)-1,2,3,4-tetrahydroisoquinolin-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3,4-dihydroisoquinoline-2(1H)-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(methylsulfonyl)-1,2,3,4-tetrahydroisoquinolin-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,3-dihydro-1H-benzimidazol-5-ylmethyl)pyridin-2(1H)-one;
• 1-[(1-acetyl-2,3-dihydro-1H-benzimidazol-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(1-glycoloyl-2,3-dihydro-1H-benzimidazol-5-yl)methyl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-[(3-acetyl-2,3-dihydro-1H-benzimidazol-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-1-[(1,3-diacetyl-2,3-dihydro-1H-benzimidazol-5-yl)methyl]-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-[(3-acetyl-1-glycoloyl-2,3-dihydro-1H-benzimidazol-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-{[3-acetyl-1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-{[3-acetyl-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-{[3-acetyl-1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-{[3-acetyl-1-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 1-{[3-acetyl-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(3-glycoloyl-2,3-dihydro-1H-benzimidazol-5-yl)methyl]pyridin-2(1H)-one;
• 1-[(1-acetyl-3-glycoloyl-2,3-dihydro-1H-benzimidazol-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(1,3-diglycoloyl-2,3-dihydro-1H-benzimidazol-5-yl)methyl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-glycoloyl-1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-glycoloyl-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-glycoloyl-1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-glycoloyl-1-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-glycoloyl-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-{[1-acetyl-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-glycoloyl-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-{[1,3-bis(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(2-hydroxy-2-methylpropanoyl)-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(2-hydroxy-2-methylpropanoyl)-1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxy-3-methylbutanoyl)-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(2-hydroxy-2-methylpropanoyl)-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-{[1-acetyl-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-glycoloyl-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxy-2-methylpropanoyl)-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-{[1,3-bis(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxypropanoyl)-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxy-3-methylbutanoyl)-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(N-methylglycyl)-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-{[1-acetyl-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-glycoloyl-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxy-2-methylpropanoyl)-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(3-hydroxypropanoyl)-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-{[1,3-bis(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxy-3-methylbutanoyl)-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(3-hydroxypropanoyl)-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-{[1-acetyl-3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-glycoloyl-3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(3-hydroxy-3-methylbutanoyl)-1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(3-hydroxy-3-methylbutanoyl)-1-(N-methylglycyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(3-hydroxy-3-methylbutanoyl)-1-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 1-{[1,3-bis(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(3-hydroxy-3-methylbutanoyl)-1-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-acetyl-6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(N-methylglycyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxypropanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1H-benzimidazole-1,3(2H)-dicarboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 1-{[1-acetyl-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-glycoloyl-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxy-2-methylpropanoyl)-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(N-methylglycyl)-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxypropanoyl)-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(3-hydroxy-3-methylbutanoyl)-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(methylsulfonyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 1-{[1,3-bis(methylsulfonyl)-2,3-dihydro-1H-benzimidazol-5-yl]methyl}-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-benzimidazol-2-one;
• 1-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-glycoloyl-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxy-3-methylbutanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 1-acetyl-6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-benzimidazol-2-one;
• 1,3-diacetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-benzimidazol-2-one;
• 3-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-glycoloyl-1,3-dihydro-2H-benzimidazol-2-one;
• 3-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 3-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 3-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 3-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxy-3-methylbutanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 3-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-glycoloyl-1,3-dihydro-2H-benzimidazol-2-one;
• 1-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-diglycoloyl-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-1-(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-1-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-1-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-1-(3-hydroxy-3-methylbutanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-1-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 1-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-glycoloyl-3-(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-bis(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(2-hydroxy-2-methylpropanoyl)-1-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(2-hydroxy-2-methylpropanoyl)-1-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxy-3-methylbutanoyl)-3-(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(2-hydroxy-2-methylpropanoyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(2-hydroxy-2-methylpropanoyl)-1-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 1-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-glycoloyl-3-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(2-hydroxy-2-methylpropanoyl)-3-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-bis(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxypropanoyl)-3-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxy-3-methylbutanoyl)-3-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(N-methylglycyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(N-methylglycyl)-1-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 1-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-glycoloyl-3-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(2-hydroxy-2-methylpropanoyl)-3-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxypropanoyl)-1-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-bis(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxy-3-methylbutanoyl)-3-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxypropanoyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxypropanoyl)-1-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxy-3-methylbutanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 1-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-glycoloyl-3-(3-hydroxy-3-methylbutanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-1-(2-hydroxy-2-methylpropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-1-(N-methylglycyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-1-(3-hydroxypropanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-bis(3-hydroxy-3-methylbutanoyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-1-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 3-acetyl-6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-glycoloyl-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(2-hydroxy-2-methylpropanoyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(N-methylglycyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(3-hydroxypropanoyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(²H)-yl]methyl}-3-(3-hydroxy-3-methylbutanoyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2-oxo-1H-benzimidazole-1,3(2H)-dicarboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(methylsulfonyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 6-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 1-acetyl-5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-glycoloyl-3-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(2-hydroxy-2-methylpropanoyl)-3-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(N-methylglycyl)-3-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxypropanoyl)-3-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-(3-hydroxy-3-methylbutanoyl)-3-(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-3-(methylsulfonyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-bis(methylsulfonyl)-1,3-dihydro-2H-benzimidazol-2-one;
• 3-benzyl-4-hydroxy-1-(2-phenylethyl)pyridin-2(1H)-one;
• 1-benzyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carbaldehyde;
• 1-benzyl-4-chloro-2-oxo-1,2-dihydropyridine-3-carbaldehyde;
• methyl 5-chloro-1-(4-chlorobenzyl)-6-oxo-1,6-dihydropyridine-3-carboxylate;
• 5-bromo-1-(2-chloro-6-fluorobenzyl)-3-methylpyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(4-fluorophenyl)ethynyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(4-fluorophenyl)ethynyl]-6-methylpyridin-2(1H)-one;
• methyl 3-chloro-4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate;
• 4-[(2,4-difluorobenzyl)oxy]-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile;
• 4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(trifluoromethyl)phenyl]pyridin-2(1H)-one;
• 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzaldehyde;
• 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-morpholin-4-ylphenyl)-6-methylpyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(4-methylpiperazin-1-yl)phenyl]-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic acid;
• 4-[(2,4-difluorobenzyl)oxy]-1-[4-(dimethylamino)-2,6-difluorophenyl]-6-methylpyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(2-hydroxyethyl)(methyl)amino]phenyl}-6-methylpyridin-2(1H)-one;
• methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate;
• 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid;
• 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one;
• 3-bromo-1-{[5-(Chloromethyl)pyrazin-2-yl]methyl}-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-[2-chloro-5-(hydroxymethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-hydroxyphenyl)-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(hydroxymethyl)-2-methoxyphenyl]-6-methylpyridin-2(1H)-one;
• methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{3-[(4-methylpiperazin-1-yl)carbonyl]phenyl}pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-(dimethylamino)ethyl]benzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-methoxyethyl)benzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-(dimethylamino)ethyl]-N-methylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-N-methylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-methoxyethyl)-N-methylbenzamide;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide;
• methyl 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoate;
• 4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-methylbenzoic acid;
• 1-(4-bromo-2-methylphenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-[(1-acetyl-1H-indol-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one;
• methyl 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-3,5-difluorobenzylcarbamate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one;
• 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{4-[(4-methylpiperazin-1-yl)carbonyl]benzyl}pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1H-indol-5-ylmethyl)pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-methoxyethyl)-4-methylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N,4-trimethylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-methyl-5-(morpholin-4-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(1-hydroxy-1-methylethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 1-(2-bromobenzyl)-3-[(2-bromobenzyl)oxy]pyridin-2(1H)-one;
• 1-(2-bromobenzyl)-3-[(2-bromobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(4-methoxybenzyl)-4-phenoxypyridin-2(1H)-one;
• 1-benzyl-2-oxo-4-phenoxy-1,2-dihydropyridine-3-carbaldehyde;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(3-dimethylaminomethyl-benzyl)-6-methyl-1H-pyridin-2-one;
• N-{3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzyl}-2-hydroxy-acetamide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-[4-(piperidine-1-carbonyl)-benzyl]-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-[(ethoxyamino)methyl]pyridin-2(1H)-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-isopropyl-benzamide;
• N-(3-aminopropyl)-4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide hydrochloride;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N,N-bis-(2-hydroxy-ethyl)-benzamide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-[4-(pyrrolidine-1-carbonyl)-benzyl]-1H-pyridin-2-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-hydroxy-benzamide;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-methyl-benzamide;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-(2-dimethylamino-ethyl)-benzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(1H-indazol-5-ylmethyl)pyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-[4-(4-methyl-piperazine-1-carbonyl)-benzyl]-1H-pyridin-2-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzaldehyde;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(4-dimethylaminomethyl-benzyl)-6-methyl-1H-pyridin-2-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-methoxyethyl)-4-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2-(dimethylamino)-4,6-difluorophenyl]-6-methylpyridin-2(1H)-one hydrochloride;
• N-(2-aminoethyl)-4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide hydrochloride;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-(2-hydroxy-ethyl)-benzamide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(4-hydroxymethyl-benzyl)-6-methyl-1H-pyridin-2-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(4-methylpiperazin-1-yl)phenyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2-(dimethylamino)-4,6-difluorophenyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(4-methylpiperazin-1-yl)phenyl]-6-methylpyridin-2(1H)-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-(2-methoxy-ethyl)-benzamide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-{4-[(2-hydroxy-ethylamino)-methyl]-benzyl}-6-methyl-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-[(dimethylamino)methyl]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-methyl-5-(morpholin-4-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(4-methylaminomethyl-benzyl)-1H-pyridin-2-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-[4-(morpholine-4-carbonyl)-benzyl]-1H-pyridin-2-one;
• N-(2-aminoethyl)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide;
• N-(3-aminopropyl)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide hydrochloride;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-(2-methoxy-ethyl)-N-methyl-benzamide;
• 1-(4-Aminomethyl-benzyl)-3-bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-(piperazin-1-ylcarbonyl)benzyl]pyridin-2(1H)-one hydrochloride;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-[4-(isopropylamino-methyl)-benzyl]-6-methyl-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-dimethylphenyl)-6-methylpyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-{3-[(2-hydroxy-ethylamino)-methyl]-benzyl}-6-methyl-1H-pyridin-2-one;
• 1-(3-Aminomethyl-benzyl)-3-bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1H-pyridin-2-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(4-hydroxy-benzyl)-6-methyl-1H-pyridin-2-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-[(dimethylamino)methyl]pyridin-2(1H)-one;
• N-{3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]benzyl}-acetamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(2-hydroxyethyl)(methyl)amino]phenyl}-6-methylpyridin-2(1H)-one;
• ethyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate;
• 1-[3-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one trifluoroacetate;
• 1-(3-{[Bis-(2-hydroxy-ethyl)-amino]-methyl}-benzyl)-3-bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1H-pyridin-2-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-[3-(isopropylamino-methyl)-benzyl]-6-methyl-1H-pyridin-2-one;
• {3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzyl}-carbamic acid tert-butyl ester;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-[4-(1-hydroxy-1-methyl-ethyl)-benzyl]-6-methyl-1H-pyridin-2-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(3-dimethylaminomethyl-benzyl)-1H-pyridin-2-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(3-piperidin-1-ylmethyl-benzyl)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-{[(2-methoxyethyl)amino]methyl}pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,4-difluoro-6-[(2-hydroxyethyl)(methyl)amino]phenyl}-6-methylpyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(3-morpholin-4-ylmethyl-benzyl)-1H-pyridin-2-one;
• 3-bromo-1-(2,6-dimethylphenyl)-6-methyl-4-[(2,4,6-trifluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(2,6-dimethylphenyl)-6-methyl-4-[(2,4,6-trifluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-(4-{[Bis-(2-hydroxy-ethyl)-amino]-methyl}-benzyl)-3-bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-morpholin-4-ylphenyl)-6-methylpyridin-2(1H)-one;
• 4-Benzyloxy-3-bromo-1-(4-fluoro-benzyl)-1H-pyridin-2-one;
• 4-[3-Chloro-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N,4-trimethylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-isopropylbenzamide;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzamide;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzonitrile;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(3-piperazin-1-ylmethyl-benzyl)-1H-pyridin-2-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-(2-hydroxy-ethyl)-N-methyl-benzamide;
• methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-chlorobenzoate;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-[3-(morpholine-4-carbonyl)-benzyl]-1H-pyridin-2-one;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N,N-bis-(2-hydroxy-ethyl)-benzamide;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzoic acid methyl ester;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-hydroxy-benzamide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(3-hydroxymethyl-benzyl)-6-methyl-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(3-fluoro-benzyl)-1H-pyridin-2-one;
• N-{3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzyl}-methanesulfonamide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-[3-(pyrrolidine-1-carbonyl)-benzyl]-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• N-(3-aminopropyl)-3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(3-methylaminomethyl-benzyl)-1H-pyridin-2-one;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-dichlorobenzenesulfonamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(dimethylamino)-2,6-difluorophenyl]-6-methylpyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(4-piperidin-1-ylmethyl-benzyl)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• N-(2-aminoethyl)-3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide hydrochloride;
• 3-bromo-1-[2-chloro-5-(hydroxymethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one;
• 3-chloro-1-[2-chloro-5-(hydroxymethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide;
• 2-{3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}-acetamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[3-(piperazin-1-ylcarbonyl)benzyl]pyridin-2(1H)-one hydrochloride;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzoic acid methyl ester;
• 1-(3-Aminomethyl-2-fluoro-benzyl)-3-bromo-4-(2,4-difluoro-benzyloxy)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(morpholin-4-ylmethyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-fluorobenzyl)pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(H-indol-5-ylmethyl)pyridin-2(1H)-one;
• 1-[3-(aminomethyl)benzyl]-3-bromo-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one trifluoroacetate;
• 1-[3-(2-aminoethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one trifluoroacetate;
• 1-[3-(aminomethyl)benzyl]-3-bromo-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)benzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(4-methoxy-benzyl)-6-methyl-1H-pyridin-2-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N,N-dimethyl-benzamide;
• 3-bromo-6-methyl-1-(pyridin-4-ylmethyl)-4-[(2,4,6-trifluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzamide;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-methyl-benzamide;
• {3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzyl}-carbamic acid methyl ester;
• 3-bromo-4-[(2,6-difluorobenzyl)oxy]-1-(2,6-dimethylphenyl)-6-methylpyridin-2(1H)-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzonitrile;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-bromo-6-methylpyridin-2(1H)-one;
• 1-Benzyl-4-benzyloxy-3-bromo-6-methyl-1H-pyridin-2-one;
• 1-benzyl-4-(benzyloxy)-3-bromo-6-methylpyridin-2(1H)-one;
• 1-Benzyl-3-bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1H-pyridin-2-one;
• {3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}-acetonitrile;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-(2-hydroxy-ethyl)-benzamide;
• 3-Chloro-4-(2,4-difluoro-benzyloxy)-1-(3-fluoro-benzyl)-1H-pyridin-2-one;
• 1-Allyl-3-chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-1H-pyridin-2-one;
• 3-Chloro-4-(2,4-difluoro-benzyloxy)-1-[4-(isopropylamino-methyl)-benzyl]-1H-pyridin-2-one;
• methyl 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(4-piperazin-1-ylmethyl-benzyl)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N,N-dimethyl-benzamide;
• 3-bromo-1-(3-fluorobenzyl)-4-[(3-methylbenzyl)oxy]pyridin-2(1H)-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-(3-methyl-benzyloxy)-1H-pyridin-2-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1,2,3,4-tetrahydroisoquinolin-5-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(3-methylbenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(isoquinolin-5-ylmethyl)pyridin-2(1H)-one trifluoroacetate;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(4-methylpiperazin-1-yl)carbonyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one trifluoroacetate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 1-allyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-methoxy-6-methylphenyl)-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-methoxy-6-methylphenyl)-6-methylpyridin-2(1H)-one;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(trifluoromethyl)phenyl]pyridin-2(1H)-one;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzoic acid;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(4-morpholin-4-ylmethyl-benzyl)-1H-pyridin-2-one;
• 4-(2,4-Difluoro-benzyloxy)-1-(3-fluoro-benzyl)-3-iodo-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-hydroxybenzamide;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(2,6-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-benzonitrile;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[3-(pyrrolidin-1-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-fluorobenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-methylbenzyl)pyridin-2(1H)-one;
• 3-{[3-chloro-4-[(2,4-difluorobenzyl)amino]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-N-isopropyl-benzamide;
• 3-bromo-1-(4-bromo-2,6-difluorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-chlorobenzyl)pyridin-2(1H)-one;
• 4-Benzyloxy-3-bromo-1-(4-chloro-benzyl)-1H-pyridin-2-one;
• 3-bromo-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-Bromo-1-(4-fluoro-benzyl)-4-(4-fluoro-benzyloxy)-1H-pyridin-2-one;
• methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate;
• 4-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-benzoic acid;
• 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzoic acid;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(2-fluorobenzyl)pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one;
• N-(2-aminoethyl)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide hydrochloride;
• 4-Benzyloxy-3-bromo-1-(4-methylsulfanyl-benzyl)-1H-pyridin-2-one;
• 1-Benzyl-4-benzyloxy-3-chloro-1H-pyridin-2-one;
• 4-(benzyloxy)-3-bromo-1-[4-(methylthio)benzyl]pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-chloropyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(2,6-dimethylphenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(2,6-dimethylphenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-[3-(isopropylamino-methyl)-benzyl]-1H-pyridin-2-one;
• 3-[3-Chloro-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-2-fluoro-benzamide;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2,3-dihydroxypropyl)pyrazine-2-carboxamide;
• {3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}-acetic acid ethyl ester;
• 4-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-N-hydroxy-benzamidine;
• 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}-N′-hydroxybenzenecarboximidamide;
• ethyl 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(3-methoxy-benzyl)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(3-methoxybenzyl)pyridin-2(1H)-one;
• 4-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-benzoic acid methyl ester;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(4-dimethylaminomethyl-benzyl)-1H-pyridin-2-one;
• 3-Chloro-4-(2,4-difluoro-benzyloxy)-1-(3-methanesulfonyl-benzyl)-1H-pyridin-2-one;
• 4-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-benzoic acid methyl ester;
• methyl 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• ethyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate;
• 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 4-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-benzonitrile;
• {3-[3-Bromo-4-(4-fluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzyl}-carbamic acid tert-butylester;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(1-hydroxy-1-methylethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(2,6-dichlorophenyl)-6-methylpyridin-2(1H)-one;
• 1-(3-Aminomethyl-benzyl)-4-benzyloxy-3-bromo-1H-pyridin-2-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-bromobenzyl)pyridin-2(1H)-one;
• 4-Benzyloxy-3-bromo-1-(4-bromo-benzyl)-1H-pyridin-2-one;
• 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one;
• 4-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-benzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[3-(piperazin-1-ylcarbonyl)phenyl]pyridin-2(1H)-one hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)amino]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-(4-fluoro-benzyloxy)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[3-(morpholin-4-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• 3-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-benzoic acid methyl ester;
• 3-bromo-1-(3-fluorobenzyl)-4-{[2-(hydroxymethyl)benzyl]oxy}pyridin-2(1H)-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-(2-hydroxymethyl-benzyloxy)-1H-pyridin-2-one;
• 1-Benzo[1,3]dioxol-5-ylmethyl-3-bromo-4-(2,4-difluoro-benzyloxy)-1H-pyridin-2-one;
• 3-bromo-4-[(2,6-difluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(3-chlorobenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(3-chlorobenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-Bromo-4-(3-chloro-benzyloxy)-1-(3-fluoro-benzyl)-1H-pyridin-2-one;
• 4-(benzyloxy)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 4-Benzyloxy-3-bromo-1-(3-fluoro-benzyl)-1H-pyridin-2-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-[3-(piperidine-1-carbonyl)-benzyl]-1H-pyridin-2-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N-dimethylbenzamide;
• 3-[3-Chloro-4-(2,4-difluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-2-fluoro-benzoic acid methyl ester;
• 1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]-3-iodopyridin-2(1H)-one;
• 1-(3-Fluoro-benzyl)-4-(4-fluoro-benzyloxy)-3-iodo-1H-pyridin-2-one;
• N-(3-aminopropyl)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide hydrochloride;
• 4-{[3-bromo-4-[(4-fluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 4-[3-Bromo-4-(4-fluoro-benzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzonitrile;
• 3-Bromo-1-(3-fluoro-benzyl)-4-(2,3,4-trifluoro-benzyloxy)-1H-pyridin-2-one;
• 1-benzyl-4-(benzyloxy)-3-bromopyridin-2(1H)-one;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)-N-methylpyrazine-2-carboxamide;
• 4-(4-Benzyloxy-3-bromo-2-oxo-2H-pyridin-1-ylmethyl)-benzonitrile;
• 3-bromo-1-(2,4-difluorobenzyl)-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-Bromo-1-(2,4-difluoro-benzyl)-4-(2,4-difluoro-benzyloxy)-1H-pyridin-2-one;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)benzamide;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 1-Benzyl-4-benzyloxy-3-bromo-1H-pyridin-2-one;
• 3-bromo-1-(Cyclopropylmethyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-(4-Aminomethyl-benzyl)-4-benzyloxy-3-bromo-1H-pyridin-2-one;
• 3-bromo-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)amino]-6-methylpyridin-2(1H)-one;
• 3-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzoic acid methyl ester;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylpyrazine-2-carboxamide;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-6-methyl-1-(pyridin-2-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-dimethylphenyl)-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-(4-bromobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-hydroxy-1-(4-hydroxybenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[2-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 1-benzyl-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(piperidin-3-ylmethyl)pyridin-2(1H)-one hydrochloride;
• 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate;
• 4-(benzylamino)-1-(3-fluorobenzyl)-6-methyl-3-nitropyridin-2(1H)-one;
• tert-butyl 4-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]piperazine-1-carboxylate;
• ethyl [4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]acetate;
• N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]benzenesulfonamide;
• 3-bromo-4-[(4-tert-butylbenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-1-phenylmethanesulfonamide;
• 1-(biphenyl-2-ylmethyl)-3-bromo-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-(biphenyl-2-ylmethoxy)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorophenyl)amino]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 4-anilino-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• methyl 4-{[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]amino}benzoate;
• 3-bromo-1-(3-fluorobenzyl)-4-[(3,4,5-trimethoxyphenyl)amino]pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[4-(4-fluorophenyl)piperazin-1-yl]pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-(4-methylpiperazin-1-yl)pyridin-2(1H)-one trifluoroacetate;
• N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-2,5-difluorobenzamide;
• N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-2,4-difluorobenzamide;
• 3-bromo-1-(Cyclohexylmethyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]propanoic acid;
• N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-N′-(2,4-difluorophenyl)urea;
• 3-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]propanamide;
• 4-(benzyloxy)-3-bromo-1-(3-morpholin-4-yl-3-oxopropyl)pyridin-2(1H)-one;
• N-(3-aminopropyl)-3-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]propanamide hydrochloride;
• 4-(benzyloxy)-3-bromo-1-(3-oxo-3-piperazin-1-ylpropyl)pyridin-2(1H)-one hydrochloride;
• 4-(benzyloxy)-3-bromo-1-(2-morpholin-4-ylethyl)pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-{[4-fluoro-2-(trifluoromethyl)benzyl]amino}pyridin-2(1H)-one;
• N-(2-aminoethyl)-3-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]propanamide hydrochloride;
• [3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]acetic acid;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(tetrahydrofuran-2-ylmethyl)pyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(tetrahydrofuran-2-ylmethyl)pyridin-2(1H)-one;
• methyl 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridine-1(2H)-carboxylate;
• 1-allyl-3-(2,4-difluorobenzyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-(2,2-diethoxyethyl)pyridin-2(1H)-one;
• methyl N-acetyl-3-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]alaninate;
• benzyl N-acetyl-3-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]alaninate;
• benzyl N-[(benzyloxy)carbonyl]-3-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]alaninate;
• 4-(benzyloxy)-1-(2-oxopropyl)pyridin-2(1H)-one;
• 5-{[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]methyl}-5-methylimidazolidine-2,4-dione;
• ethyl [4-(benzyloxy)-2-oxopyridin-1(2H)-yl]acetate;
• 2-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]acetamide;
• 1-benzyl-4-(benzyloxy)-3,5-dibromopyridin-2(1H)-one;
• 4-(benzyloxy)-1-ethylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-(4-tert-butylbenzyl)pyridin-2(1H)-one;
• 4-{[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• tert-butyl 3-{[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]methyl}piperidine-1-carboxylate;
• 1,3-dibenzyl-4-hydroxy-6-methylpyridin-2(1H)-one;
• 1-benzyl-6-methyl-2-oxo-1,2-dihydropyridin-4-yl methanesulfonate;
• 4-(benzyloxy)-1-(4-bromobenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromopyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[2-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 1-benzyl-4-(1-naphthylmethoxy)pyridin-2(1H)-one;
• 1-benzyl-4-(benzylthio)-3,5-dibromopyridin-2(1H)-one;
• 1-benzyl-4-[(2,6-dichlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-3-[(benzylamino)methyl]-4-(benzyloxy)pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-{[(2-cyclohexylethyl)amino]methyl}pyridin-2(1H)-one;
• 1-benzyl-4-(benzylthio)-5-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-6-methyl-2-oxo-1,2-dihydropyridin-4-yl methanesulfonate;
• 1-benzyl-3-bromo-6-methyl-4-{[2-(trifluoromethyl)benzyl]oxy}pyridin-2(1H)-one;
• 1-benzyl-6-methyl-2-oxo-1,2-dihydropyridin-4-yl 4-bromobenzenesulfonate;
• 1-benzyl-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-6-methyl-2-oxo-1,2-dihydropyridin-4-yl 4-bromobenzenesulfonate;
• 4-phenoxy-1-{[2-(trimethylsilyl)ethoxy]methyl}pyridin-2(1H)-one;
• 1-benzyl-4-phenoxypyridin-2(1H)-one;
• 1-(4-methoxybenzyl)-4-phenoxypyridin-2(1H)-one;
• 3-bromo-4-hydroxy-1-(4-hydroxybenzyl)pyridin-2(1H)-one hydrochloride;
• 4-(benzyloxy)-3-bromo-1-(piperidin-3-ylmethyl)pyridin-2(1H)-one;
• 1-benzyl-4-[(2,6-dichlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3,5-dibromopyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(E)-2-(4-fluorophenyl)vinyl]pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-2-oxo-1,2-dihydropyridine-3-carbaldehyde;
• 1-benzyl-4-(benzyloxy)pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)pyridin-2(1H)-one;
• 1-benzyl-4-(benzylthio)pyridin-2(1H)-one;
• methyl 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzoate;
• benzyl(5-nitro-2,6-dioxo-3,6-dihydropyrimidin-1(2H)-yl)acetate;
• ethyl 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,2′-bipyridine-5′-carboxylate;
• 4-(benzyloxy)-1-(4-methylbenzyl)pyridin-2(1H)-one;
• [5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridin-3-yl]methyl carbamate;
• 4-(benzyloxy)-1-(4-chlorobenzyl)pyridin-2(1H)-one;
• methyl(2E)-4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]but-2-enoate;
• 4-(benzyloxy)-1-(2-fluorobenzyl)pyridin-2(1H)-one;
• tert-butyl 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}piperidine-1-carboxylate;
• 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-(1,2-dihydroxyethyl)-6-methylpyridin-2(1H)-one;
• 1-benzyl-4-hydroxy-6-methylpyridin-2(1H)-one;
• 4-({[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)benzonitrile;
• 1-benzyl-4-(benzyloxy)-6-methylpyridin-2(1H)-one;
• 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde oxime;
• 1-benzyl-4-(benzylthio)-3-methylpyridin-2(1H)-one;
• 1-benzyl-4-[(4-methylbenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3,5-dibromo-6-methylpyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3,5-dibromo-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-(1-phenylethoxy)pyridin-2(1H)-one;
• 4-(benzyloxy)-1-[4-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 2-({[3-bromo-2-oxo-1-(pyridin-3-ylmethyl)-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzonitrile;
• 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbonitrile;
• 4-(benzyloxy)-1-(3-fluorobenzyl)-3-(trifluoromethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methyl-5-oxiran-2-ylpyridin-2(1H)-one;
• 1-benzyl-4-[(3-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-4-[(3-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde;
• tert-butyl 3-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}piperidine-1-carboxylate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methyl-5-vinylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-[4-(trifluoromethoxy)benzyl]pyridin-2(1H)-one;
• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-[2-(phenylthio)ethyl]pyridin-2(1H)-one;
• 3-Bromo-4-(4-chloro-benzyloxy)-1-(2-phenylsulfanyl-ethyl)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-morpholin-4-ylethyl)pyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one;
• 4-{[2-(Aminomethyl)-4-fluorobenzyl]oxy}-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate;
• 4-(benzyloxy)-1-(4-fluorobenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-1-(4-fluorobenzyl)pyridin-2(1H)-one;
• 4-Benzyloxy-3-bromo-1-methanesulfonyl-1H-pyridin-2-one;
• tert-butyl 4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]piperidine-1-carboxylate;
• 1-benzyl-4-(benzyloxy)-3-vinylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-[4-(methylthio)benzyl]pyridin-2(1H)-one;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(2-methyl-4-methylamino-pyrimidin-5-ylmethyl)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-{[2-(trifluoromethyl)benzyl]oxy}pyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-{[2-(trifluoromethyl)benzyl]oxy}pyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-[4-(methylsulfonyl)benzyl]pyridin-2(1H)-one;
• 4-Phenoxy-1H-pyridin-2-one;
• 1-benzyl-4-[(2-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-4-[(2-chlorobenzyl)oxy]pyridin-2(1H)-one;
• methyl 4-{[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one;
• 1-(3-fluorobenzyl)-4-(phenylethynyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(piperidin-4-ylmethyl)pyridin-2(1H)-one hydrochloride;
• 4-(benzyloxy)-3-bromo-1-(piperidin-4-ylmethyl)pyridin-2(1H)-one hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(methylthio)pyrimidin-4-yl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-piperidin-4-ylpyridin-2(1H)-one hydrochloride;
• 4-Benzyloxy-1-difluoromethyl-1H-pyridin-2-one;
• 4-Benzyloxy-3-bromo-1-(2-chloro-phenyl)-6-methyl-1H-pyridin-2-one;
• 3-Bromo-6-methyl-1-pyridin-3-ylmethyl-4-[(pyridin-3-ylmethyl)-amino]-1H-pyridin-2-one;
• 1-(3,4-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (2,4-difluoro-phenyl)-amide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (2,4-difluoro-phenyl)-amide;
• 5-Chloro-1-(2,6-dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (2,4-difluoro-phenyl)-amide;
• 5-Chloro-1-(2,6-dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid methyl-phenyl-amide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid benzylamide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (3-dimethylamino-propyl)-amide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (2-morpholin-4-yl-ethyl)-amide;
• N-[5-Acetyl-1-(4-chloro-benzyl)-6-methyl-2-oxo-1,2-dihydro-pyridin-3-yl]-4-chloro-benzamide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid N′-(3-chloro-5-trifluoromethyl-pyridin-2-yl)-hydrazide;
• N-allyl-2-[(1-benzyl-6-oxo-1,6-dihydropyridin-3-yl)carbonyl]hydrazinecarbothioamide;
• 1-Benzyl-5-[5-(3,4-dichloro-benzylsulfanyl)-[1,3,4]oxadiazol-2-yl]-1H-pyridin-2-one;
• N′-{[(1-benzyl-6-oxo-1,6-dihydropyridin-3-yl)carbonyl]oxy}pyridine-4-carboximidamide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid 3-trifluoromethyl-benzylamide;
• 1-Benzyl-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (2-morpholin-4-yl-ethyl)-amide;
• 5-[4-(3-Chloro-phenyl)-piperazine-1-carbonyl]-1-(3,4-dichloro-benzyl)-1H-pyridin-2-one;
• 5-Chloro-1-(2,6-dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid benzylamide;
• 1-(4-Chloro-benzyl)-5-[3-(4-chloro-phenyl)-[1,2,4]oxadiazol-5-yl]-1H-pyridin-2-one;
• 1-(4-Chloro-benzyl)-5-[3-(4-chloro-phenyl)-[1,2,4]oxadiazol-5-yl]-1H-pyridin-2-one;
• 2-Chloro-N-[1-(2,6-dichloro-benzyl)-6-oxo-5-trifluoromethyl-1,6-dihydro-pyridin-3-yl]-4-fluoro-benzamide;
• N-[1-(2,6-Dichloro-benzyl)-6-oxo-5-trifluoromethyl-1,6-dihydro-pyridin-3-yl]-4-isopropoxy-benzamidE;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (4-trifluoromethoxy-phenyl)-amide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (3-trifluoromethyl-phenyl)-amide;
• 5-Chloro-1-(2,6-dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (3-trifluoromethyl-phenyl)-amide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (4-chloro-phenyl)-amide;
• 1-(2,6-Dichloro-benzyl)-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (2-dimethylamino-ethyl)-amide;
• 5-Methyl-1-phenyl-1H-pyridin-2-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-(3-methoxy-phenyl)-1H-pyridin-2-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-(3-isopropyl-phenyl)-1H-pyridin-2-one;
• 3′-Bromo-1′-(3-fluoro-benzyl)-6-methoxy-1H-[3,4′]bipyridinyl-2′-one;
• 4-Benzo[1,3]dioxol-5-yl-3-bromo-1-(3-fluoro-benzyl)-1H-pyridin-2-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-thiophen-3-yl-1H-pyridin-2-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-(3-trifluoromethyl-phenyl)-1H-pyridin-2-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-naphthalen-2-yl-1H-pyridin-2-one;
• 3-Bromo-1-(3-fluoro-benzyl)-4-(4-fluoro-phenyl)-1H-pyridin-2-one;
• 1-Benzenesulfonyl-4-benzyloxy-3-bromo-1H-pyridin-2-one;
• 4-[3-Amino-1-(2,4-difluoro-phenyl)-propoxy]-3-bromo-6-methyl-1-pyridin-3-ylmethyl-1H-pyridin-2-one;
• 1-(4-Bromo-2,6-difluoro-phenyl)-4-(2,4-difluoro-benzyloxy)-6-methyl-1H-pyridin-2-one;
• 2-[1-(4-Amino-2-methyl-pyrimidin-5-ylmethyl)-3-bromo-6-methyl-2-oxo-1,2-dihydro-pyridin-4-yloxymethyl]-5-fluoro-benzonitrile;
• 4-(2,4-Difluoro-benzyloxy)-6-methyl-1-(2,4,6-trifluoro-phenyl)-1H-pyridin-2-one;
• 1-(2-Chloro-4-hydroxy-phenyl)-4-(2,4-difluoro-benzyloxy)-6-methyl-1H-pyridin-2-one;
• 3-[4-(2,4-Difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-benzoic acid methyl ester;
• 3-Bromo-1-(2,6-difluoro-phenyl)-4-methoxy-6-methyl-5-vinyl-1H-pyridin-2-one;
• 3-Bromo-1-(2,6-difluoro-phenyl)-4-methoxy-6-methyl-5-styryl-1H-pyridin-2-one;
• 1-(2,6-Difluoro-phenyl)-4-methoxy-6-methyl-5-phenethyl-1H-pyridin-2-one;
• 3-Bromo-1-(2,6-difluoro-phenyl)-4-methoxy-6-methyl-5-phenethyl-1H-pyridin-2-one;
• 1-(1H-indazol-5-yl)-4-(1H-indazol-5-ylamino)-6-methylpyridin-2(1H)-one;
• 5-Bromo-4-(2,4-difluoro-benzyloxy)-1-(2,6-difluoro-phenyl)-2-[2-(2,4-difluoro-phenyl)-ethyl]-6-oxo-1,6-dihydro-pyridine-3-carbaldehyde;
• 4-[3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-pyrimidine-2-carbonitrile;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-[1,2′]bipyridinyl-5′-carboxylic acid;
• 3-Bromo-4-(5-carboxy-pyridin-2-yloxy)-6-methyl-2-oxo-2H-[1,2′]bipyridinyl-5′-carboxylic acid;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6,6′-dimethyl-2-oxo-2H-[1,2′]bipyridinyl-3′-carbonitrile;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-[1,2′]bipyridinyl-5′-carboxylic acid methylamide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-[1,2′]bipyridinyl-5′-carboxylic acid (2-hydroxy-ethyl)-amide;
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-[1,2′]bipyridinyl-5′-carboxylic acid (2-methoxy-ethyl)-amide;
• 3-Bromo-1-(2,6-difluoro-phenyl)-4-methoxy-6-methyl-5-(4-methyl-benzyl)-1H-pyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-(1,2-dihydroxy-2-phenylethyl)-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-5′-(1-hydroxy-1-methylethyl)-6-methyl-2H-1,2′-bipyridin-2-one;
• 4-Benzyloxy-1H-pyridin-2-one;
• 4-Benzyloxy-3-methyl-1H-pyridin-2-one;
• 2-Oxo-6-phenethyl-1,2-dihydro-pyridine-3-carbonitrile;
• 2-Oxo-6-phenyl-1,2-dihydro-pyridine-3-carbonitrile;
• 6-Oxo-1,6-dihydro-[2,3′]bipyridinyl-5-carbonitrile;
• 6-Oxo-1,6-dihydro-[2,3′]bipyridinyl-5-carboxylic acid;
• 3-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzamide;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(4-methoxybenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(4-methoxybenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2-fluoro-5-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one;
• 3-chloro-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-chloro-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(3-chlorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-4-[(3,4-difluorobenzyl)oxy]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid;
• 3-bromo-1-(3-chlorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(3-chlorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-{[3-chloro-4-[(2,4-difluorobenzyl)amino]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile trifluoroacetate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(1-hydroxy-1-methylethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one;
• 4-(benzylamino)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 4-(benzylamino)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 2-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2-fluoro-6-(4-methylpiperazin-1-yl)phenyl]-6-methylpyridin-2(1H)-one trifluoroacetate;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methylbenzamide;
• 1-[2-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-[2-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[3-(piperidin-1-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(4-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-1-(3-fluorobenzyl)-3-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-[4-(benzyloxy)benzyl]-3-bromopyridin-2(1H)-one;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-hydroxybenzamide;
• 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 3-bromo-1-(Cyclopropylmethyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(Cyclopropylmethyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 2-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(methylamino)methyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one trifluoroacetate;
• 3-bromo-1-(3-fluorobenzyl)-4-[(2-methylbenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(2-methylbenzyl)oxy]pyridin-2(1H)-one;
• methyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(2-phenylethyl)pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(2-phenylethyl)pyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(4-methylbenzyl)oxy]pyridin-2(1H)-one;
• 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[3-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-[2-(hydroxymethyl)benzyl]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(5-{[(2-hydroxyethyl)(methyl)amino]methyl}pyrazin-2-yl)methyl]-6-methylpyridin-2(1H)-one trifluoroacetate (salt);
• 4-(benzyloxy)-3-bromo-1-[(6-fluoropyridin-3-yl)methyl]pyridin-2(1H)-one;
• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-(4-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-chloro-2-fluorobenzyl)amino]-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-ethylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-ethylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-ethylpyridin-2(1H)-one;
• 2-(2-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}phenyl)acetamide;
• 1-benzyl-3-bromo-4-[(2-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-[(2-chlorobenzyl)oxy]pyridin-2(1H)-one;
• methyl 2-{[3-bromo-4-[(4-fluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[2-(4-fluorophenyl)ethyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(2,6-dichlorophenyl)-4-[2-(4-fluorophenyl)ethyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{5-[(isopropylamino)methyl]-2-methylphenyl}-6-methylpyridin-2(1H)-one hydrochloride;
• 3-bromo-1-(3-fluorobenzyl)-4-(2-phenylethyl)pyridin-2(1H)-one;
• N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-N′-methylurea;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(3-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[2-(2-thienyl)ethyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[2-(2-thienyl)ethyl]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)amino]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate;
• 3-bromo-4-[(2,4-difluorobenzyl)amino]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate;
• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-(4-methoxybenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-(4-methoxybenzyl)pyridin-2(1H)-one;
• 3-bromo-1-(4-chlorobenzyl)-4-[(4-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(4-methoxybenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(3,5-dibromo-2,6-difluoro-4-hydroxyphenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethoxy)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethoxy)benzyl]pyridin-2(1H)-one;
• N′-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-N,N-dimethylurea;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-[4-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 2-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide;
• N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}morpholine-4-carboxamide;
• N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}methanesulfonamide;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-isopropylbenzamide;
• 4-(allylamino)-3-bromo-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one;
• 4-(allylamino)-3-bromo-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one;
• (4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}phenyl)acetic acid;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-(pyrrolidin-1-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-3-iodopyridin-2(1H)-one;
• 1-(biphenyl-4-ylmethyl)-3-bromo-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic acid;
• 4-(benzyloxy)-3-bromo-1-[2-(3-thienyl)ethyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-[2-(3-thienyl)ethyl]pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-[3-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-4-fluorobenzamide;
• methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzylcarbamate;
• 1-benzyl-4-(benzylthio)-3-bromopyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-tert-butylbenzyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-(4-tert-butylbenzyl)pyridin-2(1H)-one;
• N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-2-methoxyacetamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-({5-[(dimethylamino)methyl]pyrazin-2-yl}methyl)-6-methylpyridin-2(1H)-one trifluoroacetate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-(piperazin-1-ylcarbonyl)phenyl]pyridin-2(1H)-one hydrochloride;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N-bis(2-hydroxyethyl)benzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{5-[(dimethylamino)methyl]-2-methylphenyl}-6-methylpyridin-2(1H)-one hydrochloride;
• 1-benzyl-3-bromo-4-(2-phenylethyl)pyridin-2(1H)-one;
• 1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]-3-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-1-(piperidin-3-ylmethyl)pyridin-2(1H)-one trifluoroacetate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-(morpholin-4-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-1-(3-fluorobenzyl)-3-methylpyridin-2(1H)-one;
• N¹-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}glycinamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-(piperidin-1-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-2,6-difluorobenzamide;
• 2-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzonitrile;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methylpyrazine-2-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)amino]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one;
• 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic acid;
• 3-bromo-1-(3-fluorobenzyl)-4-[(3-fluorobenzyl)amino]pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-[(3-methoxybenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-1-(4-tert-butylbenzyl)-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}acetamide;
• 2-({3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}amino)-2-oxoethyl acetate;
• 1-benzyl-4-(benzyloxy)-3-methylpyridin-2(1H)-one;
• N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}urea;
• 1-benzyl-4-(benzyloxy)-3-ethylpyridin-2(1H)-one;
• N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-2-hydroxyacetamide;
• 3-bromo-4-[(4-chlorobenzyl)oxy]-1-(2-phenylethyl)pyridin-2(1H)-one;
• 3-bromo-1-(3-chlorobenzyl)-4-[(4-chlorobenzyl)oxy]pyridin-2(1H)-one;
• 1-[3-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 2-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzamide;
• 1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 1-[2-(aminomethyl)benzyl]-4-(benzyloxy)-3-bromopyridin-2(1H)-one;
• methyl 3-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]propanoate;
• 1-benzyl-4-(benzyloxy)-3-methylpyridin-2(1H)-one;
• 4-(allylamino)-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one;
• 4-(allylamino)-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-(phenylethynyl)pyridin-2(1H)-one;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N-dimethylbenzamide;
• {4-[({4-(benzyloxy)-3-bromo-1-[4—(Carboxymethyl)benzyl]-1,2-dihydropyridin-2-yl}oxy)methyl]phenyl}acetic acid;
• 4-(benzyloxy)-3-bromo-1-[3-(trifluoromethyl)benzyl]pyridin-2(1H)-one;
• 4-(benzyloxy)-3-ethynyl-1-(3-fluorobenzyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{3-[(dimethylamino)methyl]phenyl}-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-methylpyridin-2(1H)-one;
• 1-benzyl-3-bromo-4-(phenylethynyl)pyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-methylpyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-{[4-(trifluoromethyl)benzyl]oxy}pyridin-2(1H)-one;
• 4-(benzylamino)-3-bromo-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one;
• 4-[(2,4-difluorobenzyl)oxy]-1-(4-methoxybenzyl)-6-methylpyridin-2(1H)-one;
• 4-(benzyloxy)-3-bromo-1-methylpyridin-2(1H)-one hydrobromide;
• 4-(benzyloxy)-3-bromo-1-[4-(morpholin-4-ylcarbonyl)phenyl]pyridin-2(1H)-one;
• 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carboxylic acid;
• 1-benzyl-3-bromo-4-[(2,6-dichlorobenzyl)oxy]pyridin-2(1H)-one;
• 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid;
• 4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzoic acid;
• ethyl N-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-methylpyrimidin-4-yl)glycinate trifluoroacetate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methyl-5-[(E)-2-phenylvinyl]pyridin-2(1H)-one;
• 3-bromo-1-(3-fluorobenzyl)-4-{[3-(trifluoromethyl)benzyl]amino}pyridin-2(1H)-one;
• 3-bromo-4-[(4-fluorobenzyl)oxy]-1-(3-phenylpropyl)pyridin-2(1H)-one;
• 3-bromo-1-(4-tert-butylbenzyl)-4-[(4-fluorobenzyl)oxy]pyridin-2(1H)-one;
• 4-(allylamino)-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one;
• 1-cyclohexyl-4-[(2,4-difluorobenzyl)oxy]-3,6-dimethylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-(hydroxymethyl)-6-methylpyridin-2(1H)-one;
• 1-benzyl-4-(benzyloxy)-2-oxo-1,2-dihydropyridine-3-carbaldehyde;
• 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-prop-2-yn-1-ylpyridin-2(1H)-one;
• ethyl 3-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]propanoate;
• 1-benzyl-4-(benzyloxy)-3-(hydroxymethyl)pyridin-2(1H)-one;
• 3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(5-methyl-pyrazin-2-ylmethyl)-1H-pyridin-2-one
• 3-Chloro-4-(2,4-difluoro-benzyloxy)-1-(5-hydroxymethyl-pyrazin-2-ylmethyl)-6-methyl-1H-pyridin-2-one
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-(2,3-dihydro-1H-indol-5-ylmethyl)-1H-pyridin-2-one
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-1-[1-(2-hydroxy-acetyl)-2,3-dihydro-1H-indol-5-ylmethyl]-6-methyl-1H-pyridin-2-one
• 3-Bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(1H-pyrazol-3-ylmethyl)-1H-pyridin-2-one
• 3-[3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-4,N-dimethyl-benzamide
• 3-[3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-4-methyl-benzamide
• 3-[3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-4-fluoro-N-methyl-benzamide
• 4-Chloro-3-[3-chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-N-methyl-benzamide
• 3-[3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-4-fluoro-benzamide
• 4-[3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-3,N-dimethyl-benzamide
• 3-Chloro-4-(2,4-difluoro-benzyloxy)-1-[4-(1,2-dihydroxy-ethyl)-2-methyl-phenyl]-6-methyl-1H-pyridin-2-one
• N-{4-[3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}-2-hydroxy-acetamide
• 1-Hydroxy-cyclopropanecarboxylic acid 4-[3-chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzylamide
• N-{4-[3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-benzyl}-2-hydroxy-acetamide
• N-{4-[3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}-acetamide
• {2-[3-Bromo-1-(2,6-difluoro-phenyl)-6-methyl-2-oxo-1,2-dihydro-pyridin-4-yloxymethyl]-5-fluoro-benzyl}-carbamic acid ethyl ester or a pharmaceutically acceptable salt thereof.

The above names were generated using ChemDraw Ultra version 6.0.2, which is put out by CambridgeSoft.com, Cambridge, Mass.; or ACD Namepro version 5.09, which is put out by ACDlabs.com.

Embodiment 75. A compound according to Embodiment 17, wherein Z₅ is C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, halogen, C₁-C₆ alkoxycarbonyl, CF₃, or C₁-C₆ alkanoyl.

Embodiment 76. A compound according to Embodiment 17, wherein

• Z₅ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, or —NR₆R₇, CF₃, or C₁-C₄ alkanoyl, wherein
• R₆ and R₇ at each occurrence are independently H, C₁-C₆ alkyl optionally substituted with 1, 2, or 3 groups that are independently C₁-C₄ alkoxycarbonyl, halogen, C₃-C₆ cycloalkyl, OH, SH, or C₁-C₄ alkoxy.

Embodiment 77. A compound according to Embodiment 1, wherein

• R₁ is halogen, C₁-C₄ alkyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkenyl optionally substituted with C₁-C₄ alkoxycarbonyl, C₂-C₄ alkynyl, or carboxaldehyde;
• R₃ is H; and
• R₄ is H, alkyl optionally substituted with one or two groups that are independently CO₂R, OH, —CO₂alkyl, —C(O)NR₆R₇, —OC(O)NR₆R₇, —OC(O)—(C₁-C₆ alkyl), —C(O)R₆, —N(R₃₀)C(O)NR₆R₇, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇, —C(O)NR₆R₇, phenyl(C₁-C₆)alkoxy, phenyl(C₁-C₆)alkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein
  • the phenyl groups are unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently halogen, hydroxy, alkoxy, alkyl, nitro, CF₃, OCF₃.

Embodiment 78. A compound according to Embodiment 77, wherein

• R₂ is —OSO₂-phenyl, phenylalkoxy, phenyloxy, phenylthioalkoxy, phenylalkynyl, phenyloxy(C₁-C₆)alkyl, —OC(O)NH(CH₂)_nphenyl, —OC(O)N(alkyl)(CH₂)_nphenyl, pyridyl, pyrimidyl, thienyl, piperazinyl, imidazolidinyl, pyrrolidinyl, piperidinyl, tetrahydropyranyl, or tetrahydrofuranyl, wherein
  • each of the above is substituted with 1, 2, 3, 4, or 5 groups wherein at least one group is of the formula —(C₁-C₄ alkyl)-NR₆C(O)NR₇—(C₁-C₆ alkoxy), —(C₁-C₄ alkyl)-NR₆C(O)NR₇—(C₁-C₆ alkyl) (C₁-C₄ alkyl)-NR₁₆C(O)NR₁₇—(C₃-C₆ cycloalkylalkyl), —(C₁-C₄ alkyl)-NR₁₆C(O)NR₁₇-(heteroaryl) wherein the heteroaryl group is optionally substituted with C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen or OH, haloalkyl, or —(C₁-C₄ alkyl)-NR₁₆C(O)NR₁₇—(C₃-C₆ cycloalkyl) and the other groups, if present, are independently halogen, —NR₆R₇, CF₃, OCF₃, C₁-C₄ alkyl, —(C₁-C₄)alkyl-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-NRC(O)NR₁₆R₁₇, CN, hydroxyalkyl, dihydroxyalkyl, —OC(O)NR₆R₇, or —(C₁-C₆)alkyl-N(R)—CO₂R₃₀, wherein
    • R₁₆ and R₁₇ at each occurrence are independently H or C₁-C₆ alkyl; or
  • R₁₆, R₁₇ and the nitrogen to which they are attached form a morpholinyl ring;
  • R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, heterocycloalkyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, phenyl, heterocyloalkylalkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
    • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, hydroxyl, hydroxy C₁-C₄ alkyl, dihydroxy C₁-C₄ alkyl, or halogen;
  • n is 0, 1, 2, 3, 4, 5 or 6;
  • R at each occurrence is independently H or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl;
  • R₃₀ is C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl.

Embodiment 79. A compound according to Embodiment 78, wherein

• R₅ is wherein
• Z₁ is H, halogen, C₁-C₄ alkyl, CF₃, C₁-C₄ hydroxyalkyl, C₁-C₄ dihydroxyalkyl, or C₁-C₄ alkoxy; and
• Z₂ is C₁-C₄ alkyl, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-C(O)NR₆R₇, —NR₆R₇, NR₆R₇(C₁-C₆ alkyl), C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, halogen, C₁-C₄ alkoxy, CO₂R, OH, C₁-C₆ alkoxycarbonyl, CF₃, or C₂-C₆ alkenyl optionally substituted with CO₂H, or —OC(O)NR₁₆R₁₇; and
• Z₃ is H, halogen, C₁-C₆ alkyl, C₁-C₆ alkoxy, alkoxyalkyl, —SO₂-alkyl or C₂-C₆ alkenyl, wherein the alkyl, alkoxy, and alkenyl portions are optionally substituted with 1, 2, or 3 groups that are independently —OC(O)NR₁₆R₁₇, —C(O)NR₁₆R₁₇, OH, NR₁₆R₁₇, wherein
  • R₆ and R₇ at each occurrence are independently H, OH, C₁-C₆ alkyl optionally substituted with a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, amino C₁-C₄ alkyl, NH(C₁-C₆ alkyl)alkyl, N(C₁-C₆ alkyl)(C₁-C₆ alkyl) C₁-C₆ alkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, C₁-C₆ alkoxy C₁-C₆ alkyl, —SO₂(C₁-C₆ alkyl), —SO₂NH₂, —SO₂NH(C₁-C₆ alkyl), —SO₂N(C₁-C₆ alkyl)(C₁-C₆ alkyl), or C₁-C₆ alkanoyl, each of which is optionally substituted with 1, 2, or 3 groups that are independently halogen, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 79a. A compound according to embodiment 79, wherein

• R₆ and R₇ are independently H, C₁-C₄ alkyl or hydroxyalkyl.

Embodiment 79b. A compound according to embodiment 79 or 79a, wherein Z₁ is H, C₁-C₄ alkyl, or fluorine.

Embodiment 80. A compound according to Embodiment 79, wherein

• R₂ is benzyloxy or phenyl C₁-C₄ thioalkoxy, each of which is substituted with 1, 2, 3, 4, or 5 groups wherein at least one group is of the formula —(C₁-C₄ alkyl)-NR₆C(O)NR₇—(C₁-C₆ alkoxy) and the other groups, if present, are independently halogen, amino, monoalkylamino, dialkylamino, CF₃, OCF₃, C₁-C₄ alkyl, CN, hydroxyalkyl, or dihydroxyalkyl, wherein
  • R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; and
    • R₁₆ and R₁₇ at each occurrence are independently H or C₁-C₆ alkyl.

Embodiment 81. A compound according to Embodiment 79, of the formula wherein

• k is 0, 1, 2, 3, or 4;
• R₁₈ is C₁-C₆ alkyl;
• R₁₉ at each occurrence is independently halogen, —NR₆R₇, CF₃, OCF₃, C₁-C₄ alkyl, —(C₁-C₄)alkyl-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-NRC(O)NR₁₆R₁₇, CN, hydroxyalkyl, dihydroxyalkyl, —OC(O)NR₆R₇, or —(C₁-C₆)alkyl-N(R)—CO₂R₃₀.

Embodiment 82. A compound according to Embodiment 77, wherein

• R₂ is benzyloxy or phenyl C₁-C₄ thioalkoxy, each of which is substituted with 1, 2, 3, 4, or 5 groups independently selected from —(C₁-C₄ alkyl)-NR₆C(O)NR₇—(C₁-C₆ alkoxy), —(C₁-C₄ alkyl)-NR₁₆C(O)NR₁₇—(C₃-C₆ cycloalkyl), halogen, amino, monoalkylamino, dialkylamino, CF₃, OCF₃, C₁-C₄ alkyl, CN, hydroxyalkyl, or dihydroxyalkyl, wherein
  • R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR₁₆R₁₇, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, OH, C₁-C₆ alkanoyl, C₃-C₆ cycloalkyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, —SO₂NR₁₆R₁₇, —SO₂—C₁-C₆ alkyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, pyridyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dionyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, hydroxyl, hydroxy C₁-C₄ alkyl, dihydroxy C₁-C₄ alkyl, or halogen;
  • R₁₆ and R₁₇ at each occurrence are independently H or C₁-C₆ alkyl; and
• R₄ is H, hydroxyalkyl, or alkyl which is optionally substituted with one or two groups that are independently CO₂R, OH, —CO₂alkyl, —C(O)NR₆R₇, —OC(O)NR₆R₇, —OC(O)-(C₁-C₆ alkyl), —C(O)R₆, —N(R₃₀)C(O)NR₆R₇, —N(R₃₀)C(O)—(C₁-C₄ alkyl)-NR₆R₇, —N(R₃₀)C(O)—(C₁-C₆)alkoxy, or —NR₆R₇.

Embodiment 83. A compound according to Embodiment 82, wherein

• R₂ is benzyloxy substituted with 1, 2, 3, or 4 groups that are independently halogen, —NR₆R₇, C₁-C₄ haloalkyl, C₁-C₄ haloalkoxy, C₁-C₄ alkyl optionally substituted with —(C₁-C₄ alkyl)-NR₆C(O)NR₇—(C₁-C₆ alkoxy), —(C₁-C₄)alkyl-C(O)NR₆R₇, R₆R₇N—(C₁-C₆ alkyl)-, —C(O)NR₆R₇, —(C₁-C₄ alkyl)-NRC(O)NR₁₆R₁₇, CN, hydroxyalkyl, dihydroxyalkyl, —OC(O)NR₆R₇, or —(C₁-C₆)alkyl-N(R)—CO₂R₃₀,
• R₅ is selected from the group consisting of H, phenyl(C₁-C₆)alkyl, (C₁-C₆)alkyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently phenyl C₁-C₄ alkoxycarbonyl, —NR₈R₉, halogen, —C(O)NR₈R₉, alkoxycarbonyl, or alkanoyl, phenyl, alkoxy, C₂-C₆ alkynyl, C₂-C₆ alkenyl optionally substituted with alkoxycarbonyl, CO₂H, or —OC(O)NR₁₆R₁₇, indolyl, indolinyl, quinolinyl, isoquinolinyl, benzothiazolyl, isoindolyl, dihydroindolyl, pyrazolyl, isobenzofuranonyl, imidazolyl, pyridyl, pyrimidyl, pyrazinyl, dihydroisoindolyl, benzimidazolyl, indolon-2-yl, indazolyl, benzimidazolyl, imidazolidine dione, pyrazolyl(C₁-C₆ alkyl), imidazolyl(C₁-C₆ alkyl), piperidinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, 1H-indazolyl(C₁-C₆)alkyl, dihydroindolon-2-yl(C₁-C₆ alkyl), isobenzofuranonyl(C₁-C₆ alkyl), benzothiazolyl(C₁-C₆ alkyl), indolinyl(C₁-C₆ alkyl), dihydrobenzimidazolyl(C₁-C₆ alkyl), or dihydrobenzoimidazolonyl(C₁-C₆ alkyl), pyridyl(C₁-C₆)alkyl, pyridazinyl(C₁-C₆)alkyl, pyrimidinyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, tetrahydrofuryl(C₁-C₆)alkyl, naphthyl(C₁-C₆)alkyl, morpholinyl(C₁-C₆)alkyl, tetrahydrofuryl(C₁-C₆)alkyl, thienyl(C₁-C₆)alkyl, piperazinyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, isoindolyl(C₁-C₆)alkyl, dihydroindolyl(C₁-C₆)alkyl, pyrazolyl(C₁-C₄)alkyl, imidazolyl(C₁-C₄)alkyl, dihydroisoindolyl(C₁-C₆)alkyl, indolon-2-yl(C₁-C₆) alkyl, morpholinyl C₁-C₆ alkyl, -pyrimidinyl-piperazinyl, -pyridinyl-piperazinyl, alkenyl, -alkenyl-CO₂-alkyl, and -alkenyl-CO₂H,
  • wherein each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently NR₁₆R₁₇, C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently NR₁₆R₁₇, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, —OC(O)NH₂, —OC(O)NHR₁₆, OH, or —OC(O)NR₁₆R₁₇, halogen, —OC(O)NR₆R₇, C₁-C₆ alkoxy optionally substituted with NR₁₆R₁₇, phenyl C₁-C₆ alkoxy, C₁-C₆ thioalkoxy, C₁-C₆ alkoxycarbonyl, CO₂R, CN, carboxaldehyde, —SO₂(C₁-C₆)alkyl optionally substituted with NR₁₆R₁₇, —SO₂NR₁₆R₁₇, amidinooxime, NR₈R₉, CN, —NR₆R₇, NR₆R₇ C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, amidino, C₁-C₄ haloalkyl, phenyl, hydroxy C₁-C₆ alkyl, C₁-C₆ dihydroxyalkyl, C₁-C₄ haloalkoxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₆R₇, C₁-C₄ alkoxy, or OH, —C(O)C(O)NR₁₆R₁₇, heterocycloalkyl or heterocycloalkylalkyl, wherein the heterocycloalkyl group is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR₁₆R₁₇, or alkanoyl optionally substituted with OH, halogen, —OC(O)—(C₁-C₆ alkyl), or C₁-C₄ alkoxy; wherein
    • each of the above phenyl or heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, amino, CF₃, or OCF₃;
    • each of the heterocycloalkyl groups is optionally substituted with 1, 2, 3, or 4 groups that are independently, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ alkanoyl, —C(O)NR₆R₇;
  • R₈ is hydrogen, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl and phenyl C₁-C₆ alkanoyl; and
  • R₉ is amino C₁-C₆ alkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl, indazolyl, and phenyl C₁-C₆ alkanoyl.

Embodiment 84. A compound according to Embodiment 83, wherein

• R₁₆ and R₁₇ at each occurrence are independently H or C₁-C₆ alkyl;
• R₆ and R₇ are independently at each occurrence H, alkyl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, —SO₂—C₁-C₆ alkyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
• R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, hydroxyl, hydroxy C₁-C₄ alkyl, dihydroxy C₁-C₄ alkyl, or halogen;
  • n is 0, 1, 2, 3, 4, 5 or 6;
• R₅ is pyridyl, pyrimidyl, pyrazinyl, pyridyl(C₁-C₆)alkyl, pyrimidinyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆)alkyl wherein each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently NR₁₆R₁₇, C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently NR₁₆R₁₇, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, —OC(O)NH₂, or —OC(O)NR₁₆R₁₇, halogen, —OC(O)NR₆R₇, C₁-C₆ alkoxy optionally substituted with NR₁₆R₁₇, phenyl C₁-C₆ alkoxy, C₁-C₆ thioalkoxy, C₁-C₆ alkoxycarbonyl, CO₂R, CN, —S(C₁-C₆)alkyl optionally substituted with NR₁₆R₁₇, —SO₂(C₁-C₆)alkyl optionally substituted with NR₁₆R₁₇, amidinooxime, NR₈R₉, CN, —NR₆R₇, NR₆R₇ C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, amidino, C₁-C₄ haloalkyl, hydroxy C₁-C₆ alkyl, C₁-C₆ dihydroxyalkyl, C₁-C₄ haloalkoxy, —C(O)C(O)NR₁₆R₁₇, heterocycloalkyl which is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, alkoxyalkyl optionally substituted with NR₁₆R₁₇, or alkanoyl optionally substituted with OH, halogen, —OC(O)—(C₁-C₆ alkyl), or C₁-C₄ alkoxy; wherein
  • each of the above phenyl or heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, amino, CF₃, or OCF₃;
  • each of the heterocycloalkyl groups is optionally substituted with 1, 2, 3, or 4 groups that are independently, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ alkanoyl, —C(O)NR₆R₇;
  • R₈ is hydrogen, C₁-C₄ alkyl, C₁-C₄ alkanoyl, benzyl, and phenyl C₁-C₄ alkanoyl and
  • R₉ is amino C₁-C₆ alkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl, indazolyl, and phenyl C₁-C₆ alkanoyl.

Embodiment 85. A compound according to Embodiment 84, wherein

• R₁ is halogen;
• R₄ is hydroxyalkyl or C₁-C₄ alkyl optionally substituted with one or two groups that are independently CO₂R, —CO₂alkyl, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)NH(C₁-C₆ alkyl)(C₁-C₆ alkyl), —C(O)-C₁-C₆ alkyl, —N(R₃₀)C(O)NR₁₆R₁₇, or —N(R₃₀)C(O)—(C₁-C₆)alkoxy;
• R₅ is pyridyl, pyrimidyl, pyrazinyl, pyridyl(C₁-C₆)alkyl, pyrimidinyl(C₁-C₆)alkyl, or pyrazinyl(C₁-C₆)alkyl,
  • wherein each of the above is unsubstituted or substituted with 1, 2, or 3, groups that are independently NR₁₆R₁₇, C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently NR₁₆R₁₇, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, —OC(O)NH₂, or —OC(O)NR₁₆R₁₇, halogen, —OC(O)NR₆R₇, C₁-C₆ alkoxy optionally substituted with NR₁₆R₁₇, —SO₂(C₁-C₆ alkyl) optionally substituted with NR₁₆R₁₇, —SO₂(C₁-C₆)alkyl optionally substituted with NR₁₆R₁₇, NR₈R₉, CN, NR₆R₇ C₁-C₆ alkyl, —C(O)NR₆R₇, —NR₆R₇, heterocycloalkyl which is selected from the group consisting of piperazinyl, piperidinyl, and pyrrolidinyl, or alkoxyalkyl optionally substituted with NR₁₆R₁₇, wherein
    • each of the above phenyl or heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, amino, CF₃, or OCF₃;
    • each of the heterocycloalkyl groups is optionally substituted with 1, 2, 3, or 4 groups that are independently, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ alkanoyl, —C(O)NR₆R₇;
  • R₈ is hydrogen, C₁-C₄ alkyl, C₁-C₄ alkanoyl, benzyl, and phenyl C₁-C₄ alkanoyl and
  • R₉ is amino C₁-C₆ alkyl, mono C₁-C₆ alkylamino C₁-C₆ alkyl, di C₁-C₆ alkylamino C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₆ alkyl, and phenyl C₁-C₆ alkanoyl.

Embodiment 86. A compound according to Embodiment 85, wherein

• R₅ is of the formula: wherein
• R₅₀ is NR₁₆R₁₇, alkyl optionally substituted with 1, 2, or 3 groups that are independently —NR₁₆R₁₇, —NR₁₆SO₂alkyl, or —NR₁₆CO₂C₁-C₆ alkyl, alkoxy optionally substituted with NR₁₆R₁₇, —S(C₁-C₆ alkyl) optionally substituted with NR₁₆R₁₇, —SO₂(C₁-C₆ alkyl) optionally substituted with NR₁₆R₁₇, piperazinyl optionally substituted with 1 or 2 groups that are independently H, alkyl, alkanoyl, or CONR₆R₇, -alkyl-NR₁₆SO₂phenyl wherein the phenyl group is optionally substituted with 1, 2, 3, 4 or 5 groups that are independently halogen, alkyl, alkoxy, or CONR₁₆R₁₇, alkoxyalkyl optionally substituted with NR₁₆R₁₇, or -alkyl-OC(O)NR₁₆R₁₇, NR₈R₉, CN, NR₆R₇ C₁-C₆ alkyl, —C(O)NR₆R₇, —NR₆R₇,
• R₅₁ is H C₁-C₄ alkyl, C₁-C₄ alkoxy, or halogen;
  • wherein
  • R₆ and R₇ are independently H, C₁-C₄ alkyl, hydroxyalkyl, C₁-C₆ alkanoyl, —SO₂-C₁-C₆ alkyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 87. A compound according to Embodiment 85, wherein

• R₅ is of the formula: wherein,
• R₆ and R₇ are independently H, C₁-C₄ alkyl, hydroxyalkyl, C₁-C₆ alkanoyl, —SO₂-C₁-C₆ alkyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 88. A compound according to Embodiment 85, wherein

• R₅ is of the formula: wherein
• R₅₅ is —(C₁-C₆ alkyl)-NR₆R₇, or —NR₆R₇; wherein
  • R₆ and R₇ are independently H, C₁-C₄ alkyl, hydroxyalkyl, C₁-C₆ alkanoyl, —SO₂-C₁-C₆ alkyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 88a. A compound according to embodiment 88 wherein R₆ is derived from 2-aminopropionic acid. More preferably it is derived from (2R)-aminopropionic acid.

Embodiment 88b. A compound according to embodiment 88 wherein R₆ is derived from 2-amino, 3-hydroxypropionic acid. More preferably, R₆ is derived from the (R) isomer.

Embodiment 89. A compound according to Embodiment 85, wherein

• R₅ is of the formula: wherein
• each R₆₀ is independently H, —C(O)NR₆R₇, —CO₂R, C₁-C₄ hydroxyalkyl, C₂-C₆ dihydroxyalkyl, —(C₁-C₆ alkyl)-NR₆R₇, halogen, C₂-C₆ alkenyl, CN, or —NR₆R₇, wherein
  • R₆ and R₇ are independently H, C₁-C₄ alkyl, C₁-C₆ alkanoyl, wherein the alkyl portion of each of the above is optionally substituted with OH, or halogen;
  • R at each occurrence is independently H or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl.

Embodiment 90. A compound according to Embodiment 85, wherein

• R₅ is
• R₆₀ is —SO₂-C₁-C₆ alkyl, or —(C₁-C₆ alkyl)-NR₆R₇, wherein
  • R₆ and R₇ are independently H, C₁-C₄ alkyl, C₁-C₆ alkanoyl, wherein the alkyl portion of each of the above is optionally substituted with OH, or halogen;
  • R at each occurrence is independently H or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, SH, halogen, amino; monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl; and
• R₆₁ is H or C₁-C₄ alkyl, or C₁-C₄ alkoxy, or halogen.

Embodiment 91. A compound according to Embodiment 83, wherein

• R₅ is C₂-C₆ alkenyl -alkenyl-CO₂-alkyl, and -alkenyl-CO₂H, each of which is optionally substituted with —NR₆R₇, OH, —C(O)NR₆R₇,
  • wherein R₆ and R₇ at each occurrence are independently H, alkyl optionally substituted with a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, C₁-C₆ alkanoyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, —SO₂-C₁-C₆ alkyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, CF₃, or OCF₃; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, hydroxyl, hydroxy C₁-C₄ alkyl, dihydroxy C₁-C₄ alkyl, or halogen.

Embodiment 91a. A compound according to embodiment 91, wherein R₄ is alkyl which is optionally substituted with one or two groups that are independently CO₂R, OH, —C(O)NR₆R₇, —OC(O)NR₆R₇, —OC(O)—(C₁-C₆ alkyl), or —NR₆R₇. More preferably, R₄ is methyl or C1 alkyl optionally substituted with with one or two groups that are independently CO₂R, OH, —C(O)NR₆R₇, —OC(O)NR₆R₇, —OC(O)—(C₁-C₆ alkyl), or —NR₆R₇.

Embodiment 91b. A compound according to embodiment 91a, wherein R₆ and R₇ are H, C₁-C₄ alkyl, phenyl, amino(C₁-C₄ alkyl), alkylamino(C₁-C₄ alkyl), amino(C₁-C₆ alkanoyl), and alkylamino(C₁-C₆ alkanoyl).

Embodiment 92. A compound according to Embodiment 83, wherein

• R₅ is phenyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently NR₁₆R₁₇, C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently NR₁₆R₁₇, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, —OC(O)NH₂, —OC(O)NHR₁₆, OH, or —OC(O)NR₁₆R₁₇, halogen, —OC(O)NR₆R₇, C₁-C₆ alkoxy optionally substituted with NR₁₆R₁₇, phenyl C₁-C₆ alkoxy, C₁-C₆ thioalkoxy, C₁-C₆ alkoxycarbonyl, CO₂R, CN, carboxaldehyde, —SO₂(C₁-C₆)alkyl optionally substituted with NR₁₆R₁₇, —SO₂NR₁₆R₁₇, amidinooxime, NR₈R₉, —NR₆R₇, NR₆R₇ C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, amidino, CF₃, phenyl, C₁-C₆ hydroxyalkyl, C₁-C₆ dihydroxyalkyl, OCF₃, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₆R₇, C₁-C₄ alkoxy, or OH, —C(O)C(O)NR₁₆R₁₇, heterocycloalkyl which is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR₁₆R₁₇, or alkanoyl optionally substituted with OH, halogen, —OC(O)—(C₁-C₆ alkyl), or C₁-C₄ alkoxy; wherein
  • each of the above phenyl or heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, amino, CF₃, or OCF₃;
  • each of the heterocycloalkyl groups is optionally substituted with 1, 2, 3, or 4 groups that are independently, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ alkanoyl, —C(O)NR₁₆R₁₇; wherein
  • R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, C₁-C₆ hydroxyalkyl, C₂-C₆ dihydroxyalkyl, NR₁₆R₁₇, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, OH, C₁-C₆ alkanoyl, C₃-C₆ cycloalkyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, —SO₂-C₁-C₆ alkyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, pyridyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dione, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, hydroxyl, hydroxy C₁-C₄ alkyl, dihydroxy C₁-C₄ alkyl, or halogen; and
  • R at each occurrence is independently H or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl.

Embodiment 92a. A compound according to embodiment 92, wherein R₄ is alkyl which is optionally substituted with one or two groups that are independently CO₂R, OH, —C(O)NR₆R₇, —OC(O)NR₆R₇, —OC(O)—(C₁-C₆ alkyl), —N(R₃₀)C(O)—(C₁-C₄ alkyl)-NR₆R₇, or —NR₆R₇. More preferably, R₄ is methyl or C1 alkyl optionally substituted with with one or two groups that are independently CO₂R, OH, —C(O)NR₆R₇, —OC(O)NR₆R₇, —OC(O)—(C₁-C₆ alkyl), or —NR₆R₇.

Embodiment 92b. A compound according to embodiment 92a, wherein R₆ and R₇ are H, C₁-C₄ alkyl, phenyl, amino(C₁-C₄ alkyl), alkylamino(C₁-C₄ alkyl), amino(C₁-C₆ alkanoyl), and alkylamino(C₁-C₆ alkanoyl).

Embodiment 93. A compound according to Embodiment 83, wherein

• R₅ is phenyl(C₁-C₄)alkyl, which is optionally substituted with 1, 2, 3, 4, or 5 groups that are independently NR₁₆R₁₇, C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently NR₁₆R₁₇, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, —OC(O)NH₂, —OC(O)NHR₁₆, OH, or —OC(O)NR₁₆R₁₇, halogen, —OC(O)NR₆R₇, C₁-C₆ alkoxy optionally substituted with NR₁₆R₁₇, phenyl C₁-C₆ alkoxy, C₁-C₆ thioalkoxy, C₁-C₆ alkoxycarbonyl, CO₂R, CN, carboxaldehyde, —SO₂(C₁-C₆)alkyl optionally substituted with NR₁₆R₁₇, —SO₂NR₁₆R₁₇, amidinooxime, NR₈R₉, CN, —NR₆R₇, NR₆R₇ C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, amidino, C₁-C₄ haloalkyl, phenyl, hydroxy C₁-C₆ alkyl, C₁-C₆ dihydroxyalkyl, C₁-C₄ haloalkoxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₆R₇, C₁-C₄ alkoxy, or OH, —C(O)C(O)NR₁₆R₁₇, heterocycloalkyl which is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR₁₆R₁₇, or alkanoyl optionally substituted with 1 or 2 groups that are independently OH, halogen, —OC(O)—(C₁-C₆ alkyl), or C₁-C₄ alkoxy; wherein
  • each of the above phenyl or heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, amino, CF₃, or OCF₃;
  • each of the heterocycloalkyl groups is optionally substituted with 1, 2, 3, or 4 groups that are independently, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ alkanoyl, —C(O)NR₁₆R₁₇; wherein
  • R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR₁₆R₁₇, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, OH, C₁-C₆ alkanoyl, C₃-C₆ cycloalkyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, —SO₂NR₁₆R₁₇, —SO₂-C₁-C₆ alkyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, pyridyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dione, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, hydroxyl, hydroxy C₁-C₄ alkyl, dihydroxy C₁-C₄ alkyl, or halogen; and
  • R at each occurrence is independently H or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl.

Embodiment 94. A compound according to Embodiment 83, wherein

• R₅ is selected from the group consisting of H, (C₁-C₆)alkyl optionally substituted with 1, 2, 3, 4, or 5 groups that are independently phenyl C₁-C₄ alkoxycarbonyl, —NR₈R₉, halogen, —C(O)NR₈R₉, alkoxycarbonyl, or alkanoyl, indolyl, indolinyl, quinolinyl, isoquinolinyl, benzothiazolyl, isoindolyl, dihydroindolyl, pyrazolyl, 3H-isobenzofuran-1-onyl, imidazolyl, pyridyl, pyrimidyl, pyrazinyl, furanyl, dihydroisoindolyl, indolon-2-yl, indazolyl, thienyl, benzimidazolyl, imidazolidine dione, pyrazolyl(C₁-C₆ alkyl), furanyl(C₁-C₆ alkyl), imidazolyl(C₁-C₆ alkyl), piperidinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₆)alkyl, imidazolidinyl(C₁-C₆)alkyl, 1H-indazolyl(C₁-C₆)alkyl, dihydroindolon-2-yl(C₁-C₆ alkyl), 3H-isobenzofuranonyl(C₁-C₆ alkyl), benzothiazolyl(C₁-C₆ alkyl), indolinyl(C₁-C₆ alkyl), dihydrobenzimidazolyl(C₁-C₆ alkyl), benzimidazolyl(C₁-C₆)alkyl, isochroman-4-one (C₁-C₆)alkyl, oxazolidin-2-one (C₁-C₆)alkyl, benzoxazolyl(C₁-C₆)alkyl, dihydrobenzoimidazolonyl(C₁-C₆ alkyl), pyridyl(C₁-C₆)alkyl, pyridazinyl(C₁-C₆)alkyl, pyrimidinyl(C₁-C₆)alkyl, pyrazinyl(C₁-C₆)alkyl, tetrahydrofuryl(C₁-C₆)alkyl, naphthyl(C₁-C₆)alkyl, morpholinyl(C₁-C₆)alkyl, tetrahydrofuryl(C₁-C₆)alkyl, thienyl(C₁-C₆)alkyl, piperazinyl(C₁-C₆)alkyl, indolyl(C₁-C₆)alkyl, quinolinyl(C₁-C₆)alkyl, isoquinolinyl(C₁-C₆)alkyl, dihydro-1H-isoindolyl(C₁-C₆)alkyl, dihydroindolyl(C₁-C₆)alkyl, imidazolyl(C₁-C₄)alkyl, dihydroisoindolyl(C₁-C₆)alkyl, indolon-2-yl(C₁-C₆)alkyl, morpholinyl C₁-C₆ alkyl, -pyrimidinyl-piperazinyl, and -pyridinyl-piperazinyl, wherein
  • each of the above is unsubstituted or substituted with 1, 2, 3, 4, or 5 groups that are independently NR₁₆R₁₇, C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently NR₁₆R₁₇, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, —OC(O)NH₂, —OC(O)NHR₁₆, OH, or —OC(O)NR₁₆R₁₇, halogen, —OC(O)NR₆R₇, C₁-C₆ alkoxy optionally substituted with NR₁₆R₁₇, phenyl C₁-C₆ alkoxy, C₁-C₆ thioalkoxy, C₁-C₆ alkoxycarbonyl, CO₂R, CN, carboxaldehyde, —SO₂(C₁-C₆)alkyl optionally substituted with NR₁₆R₁₇, —SO₂NR₁₆R₁₇, amidinooxime, NR₈R₉, CN, —NR₆R₇, NR₆R₇ C₁-C₆ alkyl, —C(O)NR₆R₇, —(C₁-C₄)alkyl-C(O)NR₆R₇, amidino, C₁-C₄ haloalkyl, phenyl, hydroxy C₁-C₆ alkyl, C₁-C₆ dihydroxyalkyl, C₁-C₄ haloalkoxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₆R₇, C₁-C₄ alkoxy, or OH, —C(O)C(O)NR₁₆R₁₇, heterocycloalkyl or heterocycloalkyl(C₁-C₆)alkyl, wherein the heterocycloalkyl group is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR₁₆R₁₇, or alkanoyl optionally substituted with OH, halogen, C₃-C₆ cycloalkyl, —OC(O)—(C₁-C₆ alkyl), or C₁-C₄ alkoxy; wherein
    • each of the above phenyl or heteroaryl groups are optionally substituted with 1, 2, 3, 4, or 5 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, amino, CF₃, or OCF₃;
    • each of the heterocycloalkyl groups is optionally substituted with 1, 2, 3, or 4 groups that are independently, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ alkanoyl, —C(O)NR₁₆R₁₇;
  • R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR₁₆R₁₇, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, OH, C₁-C₆ alkanoyl, C₃-C₆ cycloalkyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, —SO₂NR₁₆R₁₇, SO₂-C₁-C₆ alkyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, pyridyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dione, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, hydroxyl, hydroxy C₁-C₄ alkyl, dihydroxy C₁-C₄ alkyl, or halogen; and
  • R at each occurrence is independently H or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl.

Embodiment 95. A compound according to Embodiment 94, wherein

• R₅ is indolyl(C₁-C₆)alkyl-, indolinyl-(C₁-C₄ alkyl)-, isochroman-4-one (C₁-C₆)alkyl-, indolon-2-yl(C₁-C₆)alkyl-, benzoxazolyl(C₁-C₆)alkyl-, 3H-isobenzofuran-1-one (C₁-C₆)alkyl-, 3H-isobenzofuran-1-one, dihydro-1H-isoindolyl(C₁-C₆)alkyl, dihydroisoindolyl(C₁-C₆)alkyl, benzothiazolyl(C₁-C₆)alkyl-, benzothiazolyl, benzimidazolyl, or benzimidazolyl(C₁-C₆)alkyl-, optionally substituted with 1, 2, 3, or 4 groups that are independently C₁-C₄ alkyl, OH, —C(O)C(O)NR₁₆R₁₇, piperidinyl(C₁-C₄)alkyl, piperazinyl(C₁-C₆)alkyl, pyrrolidinyl(C₁-C₄)alkyl, NR₆R₇ C₁-C₆ alkyl, morpholinyl C₁-C₆ alkyl, C₁-C₆ alkanoyl optionally substituted with 1 or 2 groups that are independently OH, halogen, —OC(O)—(C₁-C₆ alkyl), or C₁-C₄ alkoxy, —SO₂(C₁-C₆)alkyl, C₁-C₆ alkoxycarbonyl,
• R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR₁₆R₁₇, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, OH, C₁-C₆ alkanoyl, C₃-C₆ cycloalkyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, —SO₂NR₁₆R₁₇, —SO₂-C₁-C₆ alkyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, pyridyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy.

Embodiment 96. A compound according to Embodiment 94, wherein

• R₅ is pyrazolyl C₁-C₆ alkyl, oxazolidin-2-one (C₁-C₆)alkyl, furanyl, thienyl, or furanyl C₁-C₆ alkyl, which are optionally substituted with 1 or 2 groups independently selected from the group consisting of —C(O)NR₆R₇, NR₆R₇ C₁-C₆ alkyl, C₁-C₆ alkyl, C₁-C₆ alkoxycarbonyl, (C₁-C₄)alkyl optionally substituted with 1 or 2 groups that are independently NR₁₆R₁₇, —NR₁₆SO₂-alkyl, —NR₁₆SO₂-phenyl, —OC(O)NH₂, —OC(O)NHR₁₆, OH, or —OC(O)NR₁₆R₁₇, hydroxy C₁-C₆ alkyl, heterocycloalkyl which is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, CO₂R, C₃-C₆ cycloalkyl, wherein
  • R₆ and R₇ are independently at each occurrence H, alkyl optionally substituted with NR₁₆R₁₇ or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR₁₆R₁₇, alkoxy optionally substituted with NR₁₆R₁₇, C₁-C₄ alkoxy C₁-C₄ alkyl, OH, C₁-C₆ alkanoyl, C₃-C₆ cycloalkyl, phenyl C₁-C₄ alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C₂-C₆ alkenyl optionally substituted with —OC(O)NR₁₆R₁₇, —SO₂-phenyl, —SO₂NR₁₆R₁₇, —SO₂-C₁-C₆ alkyl, phenyl, pyrrolidinyl C₁-C₄ alkanoyl, piperidinyl C₁-C₄ alkanoyl, pyridyl C₁-C₄ alkanoyl, phenyl C₁-C₄ alkoxy, phenyl C₁-C₄ alkoxycarbonyl, or phenyl C₁-C₄ alkanoyl, wherein each of the above is unsubstituted or substituted with 1, 2, or 3 groups that are independently, halogen, C₃-C₆ cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH₂, —C(O)NH(C₁-C₆ alkyl), —C(O)N(C₁-C₆ alkyl)(C₁-C₆ alkyl), C₁-C₄ alkoxy, C₁-C₄ alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C₁-C₆ alkyl, C₁-C₄ haloalkyl, or C₁-C₄ haloalkoxy; or
  • R₆, R₇, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dione, or piperazinyl ring which is optionally substituted with 1 or 2 groups that are independently C₁-C₄ alkyl, C₁-C₄ alkoxycarbonyl, hydroxyl, hydroxy C₁-C₄ alkyl, dihydroxy C₁-C₄ alkyl, or halogen; and
  • R at each occurrence is independently H or C₁-C₆ alkyl optionally substituted with 1 or 2 groups that are independently OH, halogen, amino, monoalkylamino, dialkylamino or C₃-C₆ cycloalkyl.

Embodiment 97. A compound according to Embodiment 1 that is selected from

• (2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]but-2-enoic acid;
• 3-[4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide;
• 3,5-dibromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-methyl-2-(methylsulfonyl)pyrimidin-5-yl]pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-4-(morpholin-4-ylcarbonyl)benzamide;
• 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carboxylic acid;
• 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzamide;
• 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(tetrahydro-2H-pyran-2-yloxy)benzamide;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzamide;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-3-(trifluoromethyl)benzamide;
• 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-hydroxy-4-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(1E)-3-hydroxyprop-1-en-1-yl]phenyl}-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(tetrahydro-2H-pyran-2-yloxy)benzamide;
• (2E)-3-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}prop-2-en-1-yl carbamate;
• 1-[5-(aminomethyl)-2-methylphenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride;
• N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzyl}-2-hydroxyacetamide;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(2E)-4-morpholin-4-yl-4-oxobut-2-en-1-yl]pyridin-2(1H)-one;
• tert-butyl {3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}carbamate;
• N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)urea;
• 2-[(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)amino]-1-methyl-2-oxoethyl acetate;
• methyl 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furoate;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(1-glycoloyl-2,3-dihydro-1H-indol-5-yl)methyl]pyridin-2(1H)-one;
• N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-hydroxypropanamide;
• N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-hydroxy-2-methylpropanamide;
• 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide;
• 2-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}-2-hydroxyethyl carbamate;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide;
• {1-[3-(aminocarbonyl)phenyl]-5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl carbamate;
• 2-({3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}amino)-2-oxoethyl acetate;
• 2-({3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}amino)-1,1-dimethyl-2-oxoethyl acetate;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide;
• N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N-methylurea;
• 1-[4-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[5-(morpholin-4-ylcarbonyl)-2-furyl]pyridin-2(1H)-one;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl carbamate;
• {5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furyl}methyl carbamate;
• 3-bromo-2-[2-(2-fluorophenyl)pyridin-4-yl]-1,5,6,7-tetrahydro-4H-pyrrolo[3,2-c]pyridin-4-one trifluoroacetate;
• N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-2-hydroxy-2-methylpropanamide;
• 1-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}ethane-1,2-diyl dicarbamate;
• 1-[4-(aminomethyl)-2-fluorophenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride;
• 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-2-oxoethyl acetate;
• 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-1,1-dimethyl-2-oxoethyl acetate;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-indol-2-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1H-pyrazol-3-ylmethyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(1H-pyrazol-3-ylmethyl)pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxyethyl)-1H-pyrazol-3-yl]methyl}-6-methylpyridin-2(1H)-one;
• 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzenesulfonamide;
• {1-[3-(aminocarbonyl)phenyl]-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate;
• 1-(1,3-benzoxazol-6-ylmethyl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• {1-[3-(aminocarbonyl)phenyl]-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl carbamate;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)-2-furamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[5-(morpholin-4-ylcarbonyl)-2-furyl]methyl}pyridin-2(1H)-one;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-2-furamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(4-vinylphenyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[5-(piperazin-1-ylcarbonyl)-2-furyl]methyl}pyridin-2(1H)-one;
• methyl 2-bromo-5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoate;
• N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}urea;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylamino)pyrimidin-5-yl]methyl}pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)-2-furyl]methyl}-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)phenyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[5-(piperidin-1-ylcarbonyl)-2-furyl]pyridin-2(1H)-one;
• methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzoate;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[1-(methylsulfonyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-2-oxoethyl acetate;
• 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-1,1-dimethyl-2-oxoethyl acetate
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-cyclopropyl-4-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(1H-pyrazol-3-ylmethyl)pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(methoxyacetyl)-1H-pyrazol-3-yl]methyl}-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-ethyl-4-methylbenzamide;
• N-allyl-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide;
• {1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate;
• 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]methyl}-N-methylbenzamide;
• 1-{[5-(aminomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 2-{[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]amino}-2-oxoethyl acetate;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-hydroxyacetamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(dimethylamino)pyrimidin-5-yl]methyl}-6-methylpyridin-2(1H)-one trifluoroacetate;
• methyl 3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate;
• 1-allyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-butyl-4-methylbenzamide;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile;
• N-(2-aminoethyl)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-{4-[(methylamino)methyl]benzyl}pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-isobutyl-4-methylbenzamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxy-2-methylpropyl)-1H-pyrazol-3-yl]methyl}-6-methylpyridin-2(1H)-one;
• ethyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-5-carboxylate;
• 3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]acetamide;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]methanesulfonamide;
• methyl [(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]carbamate;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-hydroxy-2-methylpropanamide;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-1-hydroxycyclopropanecarboxamide;
• N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]glycinamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)pyridin-2(1H)-one;
• 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzenesulfonamide;
• tert-butyl 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-isoindole-2-carboxylate;
• methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]-4-methylbenzoate;
• 1-{[2-(aminomethyl)pyrimidin-5-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate;
• N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)methyl]glycinamide trifluoroacetate;
• 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-hydroxy-1-(hydroxymethyl)ethyl]-4-methylbenzamide;
• methyl 5-bromo-2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-2-oxopyridin-1(2H)-yl]benzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-5-vinylphenyl)pyridin-2(1H)-one;
• 1-[(2-aminopyrimidin-5-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-methoxypyrimidin-5-yl)methyl]-6-methylpyridin-2(1H)-one;
• 3-[6-(aminomethyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzamide hydrochloride;
• methyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-vinylbenzoate;
• 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-(dimethylamino)ethyl]-4-methylbenzamide;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-vinylbenzoic acid;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carboxamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)alaninamide hydrochloride;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N²-methylglycinamide hydrochloride;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)serinamide hydrochloride;
• N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)prolinamide hydrochloride;
• dimethyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalate;
• methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-vinylbenzoate;
• methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(1,2-dihydroxyethyl)benzoate;
• 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)methyl]-2-hydroxyacetamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-methyl-1,3-dihydro-2H-indol-2-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,3-dihydro-1H-isoindol-5-ylmethyl)-6-methylpyridin-2(1H)-one trifluoroacetate;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyridine-2-carboxamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(E)-2-methoxyvinyl]phenyl}-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(Z)-2-methoxyvinyl]phenyl}-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(2-hydroxyethyl)phenyl]-6-methylpyridin-2(1H)-one;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-2-vinylbenzamide;
• 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-methyl-1,3-dihydro-2H-indol-2-one;
• methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(1-hydroxy-1-methylethyl)benzoate;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-(1,2-dihydroxyethyl)-N-methylbenzamide;
• N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-D-alaninamide hydrochloride;
• N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-N²-methylglycinamide hydrochloride;
• N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-D-serinamide hydrochloride;
• 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-isoindol-5-yl]methyl}-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-dimethyl-1,3-benzothiazol-5-yl)-6-methylpyridin-2(1H)-one;
• 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furoic acid;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoic acid;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N-dimethyl-3-(trifluoromethyl)benzamide;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzoic acid;
• 1-[5-(aminomethyl)-2-fluorophenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzoic acid;
• (2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxy-2-methylpropyl)but-2-enamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(5-hydroxy-1H-pyrazol-3-yl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-furyl]-6-methylpyridin-2(1H)-one;
• methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)methyl]benzoate;
• (−)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2-(hydroxymethyl)-5-[(methylamino)methyl]phenyl}-6-methylpyridin-2(1H)-one;
• 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-2-furamide;
• 1-[4-(aminomethyl)-2-fluorophenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-methyl-2-(methylsulfonyl)pyrimidin-5-yl]pyridin-2(1H)-one;
• 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N¹-(2-hydroxyethyl)-N⁴-methylterephthalamide;
• 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carbonitrile;
• methyl 3-[4-[(2,4-difluorobenzyl)oxy]-2-methyl-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoate;
• 5-[3-bromo-4-4[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carboxamide;
• 3-chloro-1-{[1-(Cyclopropylcarbonyl)-1H-pyrazol-3-yl]methyl}-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylthiophene-3-carboxamide;
• {1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl phenylcarbamate;
• {1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl [2-(3-thienyl)ethyl]carbamate;
• methyl 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoate;
• 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoic acid;
• 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}-N-methylbenzamide;
• 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzamide;
• (+)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{1-[4-(hydroxymethyl)phenyl]ethyl}-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-oxopropyl)pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(hydroxymethyl)-3-(1-hydroxy-1-methylethyl)phenyl]-6-methylpyridin-2(1H)-one;
• 1-[2,4-bis(1-hydroxy-1-methylethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 5-bromo-2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methylbenzamide;
• 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-5-vinylbenzamide;
• 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(1,2-dihydroxyethyl)-N-methylbenzamide;
• 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(2,2,2-trifluoroethyl)benzamide;
• 3-bromo-1-(3′-chloro-4-methylbiphenyl-3-yl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one;
• 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1H-indol-3-yl)-N,N-dimethyl-2-oxoacetamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-glycoloylphenyl)-6-methylpyridin-2(1H)-one;
• N-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)-2-hydroxy-2-methylpropanamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(piperidin-1-ylmethyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)piperidine-4-carboxamide hydrochloride;
• N²-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)glycinamide;
• N-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-hydroxy-2-methylpropanamide;
• 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-(dimethylamino)ethyl]-4-methylbenzamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(piperazin-1-ylmethyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one hydrochloride;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-D-serinamide hydrochloride;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-L-threoninamide hydrochloride;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-methylalaninamide hydrochloride;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-D-alaninamide hydrochloride;
• N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)piperidine-4-carboxamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-{[2-(dimethylamino)ethyl]amino}pyrimidin-5-yl)methyl]-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-({3-[(dimethylamino)methyl]-1H-indol-5-yl}methyl)pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-({3-[(methylamino)methyl]-1H-indol-5-yl}methyl)pyridin-2(1H)-one;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N²-methyl-L-serinamide hydrochloride;
• N-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyridin-2-yl)-2-hydroxy-2-methylpropanamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(3-{[(2-hydroxyethyl)amino]methyl}-1H-indol-5-yl)methyl]pyridin-2(1H)-one;
• N¹-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-L-serinamide hydrochloride;
• N¹-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-methylalaninamide hydrochloride;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-D-allothreoninamide hydrochloride;
• N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-2-methylalaninamide hydrochloride;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(morpholin-4-ylmethyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-({2-[(2-hydroxyethyl)amino]pyrimidin-5-yl}methyl)-6-methylpyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-({[2-(dimethylamino)ethyl]amino}methyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 1-({2-[(2-aminoethyl)amino]pyrimidin-5-yl}methyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-hydroxy-N,4-dimethylbenzamide;
• N-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)-2-hydroxyacetamide;
• 3-[3-bromo-4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide;
• 1-allyl-6-[(allylamino)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(2-hydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• N¹-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-L-threoninamide hydrochloride;
• N¹-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}glycinamide hydrochloride;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-[2-(dimethylamino)ethyl]-1H-pyrazole-5-carboxamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-{[2-hydroxy-1-(hydroxymethyl)ethyl]amino}pyrimidin-5-yl)methyl]-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methylpyridine-2-carboxamide;
• 1-{[5-(aminomethyl)-2-furyl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride;
• N-(2-{[(3-bromo-1-{5-[(2,2-dimethylhydrazino)carbonyl]-2-methylphenyl}-6-methyl-2-oxo-1,2-dihydropyridin-4-yl)oxy]methyl}-5-fluorobenzyl)-N′-ethylurea;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(pyrrolidin-1-ylmethyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-methoxyethyl)-1H-pyrazole-5-carboxamide;
• 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-2-vinylbenzamide;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-hydroxy-4-methylbenzamide;
• 3-[3-bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-N-carbamoylmethyl-benzamide;
• N¹-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-N²-methylglycinamide hydrochloride;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,5-dimethyl-1H-benzimidazol-6-yl)-6-methylpyridin-2(1H)-one;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1H-pyrazole-5-carboxamide;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2,3-dihydroxypropyl)-1H-pyrazole-5-carboxamide;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-1H-pyrazole-5-carboxamide;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,3-dihydro-1H-isoindol-5-ylmethyl)pyridin-2(1H)-one trifluoroacetate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,4′-bipyridine-2′-carboxamide;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)-1H-pyrazole-5-carboxamide;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furyl)methyl]-2-hydroxy-2-methylpropanamide;
• N¹-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}alaninamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methylprop-2-en-1-yl)pyridin-2(1H)-one;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• 5-bromo-6-[(2,4-difluorobenzyl)oxy]-3-isopropyl-2-[4-(2-methylalanyl)piperazin-1-yl]pyrimidin-4(3H)-one trifluoroacetate;
• methyl 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,4′-bipyridine-2′-carboxylate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(2-furyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one;
• N¹-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}serinamide hydrochloride;
• 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylpyridine-2-carboxamide;
• 3-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-1H-pyrazole-5-carboxamide;
• N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-D-alaninamide hydrochloride;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-[(glycylamino)methyl]-2-oxopyridin-1(2H)-yl]benzamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(4-hydroxy-1-oxo-3,4-dihydro-1H-isochromen-7-yl)-6-methylpyridin-2(1H)-one;
• 6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinamide;
• N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-methylalaninamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,4′-bipyridine-2′-carboxylic acid;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-{[(N-methylglycyl)amino]methyl}-2-oxopyridin-1(2H)-yl]benzamide hydrochloride;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxo-6-[(serylamino)methyl]pyridin-1(2H)-yl]benzamide hydrochloride;
• N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-D-serinamide hydrochloride;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(3-methyl-4-vinylphenyl)pyridin-2(1H)-one;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]urea;
• N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]piperidine-4-carboxamide hydrochloride;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethyl-1H-pyrazole-5-carboxamide;
• {5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2E)-4-hydroxybut-2-en-1-yl]-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate;
• 3-[6-[(alanylamino)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzamide hydrochloride;
• 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(3-methyl-1H-pyrazol-4-yl)pyridin-2(1H)-one;
• N-({1-[3-(aminocarbonyl)phenyl]-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl)pyridine-2-carboxamide;
• methyl 2-bromo-5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-2′-(hydroxymethyl)-6-methyl-2H-1,4′-bipyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-3-methylphenyl]-6-methylpyridin-2(1H)-one;
• N-({3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,3′-bipyridin-6′-yl}methyl)-2-hydroxy-2-methylpropanamide;
• 6′-(aminomethyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2H-1,3′-bipyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-({2-[2-(dimethylamino)ethoxy]pyrimidin-5-yl}methyl)-6-methylpyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-{[(2-methylalanyl)amino]methyl}-2-oxopyridin-1(2H)-yl]benzamide hydrochloride;
• 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-{[(2-hydroxy-2-methylpropanoyl)amino]methyl}-2-oxopyridin-1(2H)-yl]benzamide;
• 3-bromo-6′-chloro-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-2H-1,3′-bipyridin-2-one;
• 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(hydroxymethyl)-N-methylbenzamide;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-[(methylamino)carbonyl]benzyl carbamate;
• 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-[(methylamino)carbonyl]benzyl carbamate;
• 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-vinylbenzoic acid;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,3′-bipyridine-6′-carboxamide;
• methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-[(methylamino)carbonyl]benzoate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2′-vinyl-2H-1,4′-bipyridin-2-one;
• 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-(1,2-dihydroxyethyl)-N-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-6′-vinyl-2H-1,3′-bipyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(methylsulfonyl)pyrimidin-5-yl]pyridin-2(1H)-one;
• 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-formyl-N-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,3′-bipyridine-6′-carbonitrile;
• methyl 3-bromo-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-2-oxo-2H-1,3′-bipyridine-6′-carboxylate;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(2-oxo-1,3-oxazolidin-5-yl)methyl]pyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6′-(1,2-dihydroxyethyl)-5′,6-dimethyl-2H-1,3′-bipyridin-2-one;
• 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-5-[(methylamino)methyl]benzamide;
• 3-bromo-2′-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2H-1,4′-bipyridin-2-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-2-oxo-2H-1,3′-bipyridine-6′-carboxamide;
• (−)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-2′-(1,2-dihydroxyethyl)-6-methyl-2H-1,4′-bipyridin-2-one;
• 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(1-hydroxy-1-methylethyl)-N-methylbenzamide;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(3,3-dimethyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)-6-methylpyridin-2(1H)-one;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)pyridin-2(1H)-one;
• 3-[3-bromo-4-[(2,4-difluorophenoxy)methyl]-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide;
• 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluoro-N-(1-methyl-1H-pyrazol-3-yl)benzamide;
• 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-N-(Cyclopropylmethyl)-5-fluorobenzamide;
• 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylic acid;
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-5-yl]methyl}pyridin-2(1H)-one; and
• 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-5-yl]methyl}pyridin-2(1H)-one.

Embodiment 98. A compound according to Embodiment 78 of the formula: wherein,

R₁ is halogen; and Z, R₂₀, and R₃₀ are as defined below:

	Z	R20	R30
	—CH2CH3	H	H
	—CH2CH3	H
	—CH2CH3	H
	—CH2CH3	H
	—CH2CH3	H
	—CH2CH3	Me	H
	—CH2CH3	Me
	—CH2CH3	Me
	—CH2CH3	F	H
	—CH2CH3	F
	—CH2CH3	F
	—CH2CH3	F
	—CH2CH3	F
	—OCH3	H	H
	—OCH3	H
	—OCH3	H
	—OCH3	H
	—OCH3	H
	—OCH3	Me	H
	—OCH3	Me
	—OCH3	Me
	—OCH3	Me
	—OCH3	Me
	—OCH3	F	H
	—OCH3	F
	—OCH3	F
	—OCH3	F
	—OCH3	F
	—CH(CH3)2	H	H
	—CH(CH3)2	H
	—CH(CH3)2	H
	—CH(CH3)2	H
	—CH(CH3)2	H
	—CH(CH3)2	Me	H
	—CH(CH3)2	Me
	—CH(CH3)2	Me
	—CH(CH3)2	Me
	—CH(CH3)2	Me
	—CH(CH3)2	F	H
	—CH(CH3)2	F
	—CH(CH3)2	F
	—CH(CH3)2	F
	—CH(CH3)2	F

Embodiment 99. A compound according to Embodiment 78, of the formula: wherein

R₁ is halogen; and Z, R₂₀, and R₃₀ are as defined below:

	Z	R20	R30
	—CH2CH3	H	H
	—CH2CH3	H
	—CH2CH3	H
	—CH2CH3	H
	—CH2CH3	H
	—CH2CH3	Me	H
	—CH2CH3	Me
	—CH2CH3	Me
	—CH2CH3	F	H
	—CH2CH3	F
	—CH2CH3	F
	—CH2CH3	F
	—CH2CH3	F
	—OCH3	H	H
	—OCH3	H
	—OCH3	H
	—OCH3	H
	—OCH3	H
	—OCH3	Me	H
	—OCH3	Me
	—OCH3	Me
	—OCH3	Me
	—OCH3	Me
	—OCH3	F	H
	—OCH3	F
	—OCH3	F
	—OCH3	F
	—OCH3	F
	—CH(CH3)2	H	H
	—CH(CH3)2	H
	—CH(CH3)2	H
	—CH(CH3)2	H
	—CH(CH3)2	H
	—CH(CH3)2	Me	H
	—CH(CH3)2	Me
	—CH(CH3)2	Me
	—CH(CH3)2	Me
	—CH(CH3)2	Me
	—CH(CH3)2	F	H
	—CH(CH3)2	F
	—CH(CH3)2	F
	—CH(CH3)2	F
	—CH(CH3)2	F

Embodiment 100. A compound according to Embodiment 78 of the formula: wherein

Y is

CONH(CH2)nOH;
CONHCH2C(Me)2OH;
CONH(CH2)nNH2;
CONH(CH2)nNHCH3;
CONH(CH2)nN(CH3)2;
CONHCH2CH(OH)CH2OH;
CH2NHCOCH2NH2;
CH2NHCOCH2OH;
CH2NHCOCH(NH2)CH2OH;

and

• n is 1, 2, or 3.

Embodiment 101. A compound according to Embodiment 78, of the formula: wherein

R₅₀ is:

—O(CH2)nR51;
—NH(CH2)nR51;
—N(CH3)(CH2)nR51;
—S(CH2)nR51;
—SO2(CH2)nR51;

• n is 2, 3, 4;
• R₅₁ is H, OH, NH₂, NHR₅₂, CONHR₅₂, or OR₅₂;
• R₅₂ is H, C₁-C₄ alkyl;
• R₅₃ is H or alkyl.

Embodiment 102. A compound according to Embodiment 78, of the formula: wherein R₅₀ is:

• • CH₂CONH₂;
  • CH₂CONHCH₃;
  • CH₂CONH(CH₃)₂;
  • CH₂CONH(CH₂)_nNH₂;
  • CH₂CONH(CH₂)_nNHCH₃;
  • CH₂NHCONH₂;
  • CH₂NHCO(CH₂)₂NH₂;
  • CH₂NHCH₃;
  • CH₂N(CH₃)₂;
  • CH₂NHSO₂ (C₁-C₃ alkyl);
  • CH₂NHSO₂ phenyl;
  • CH₂NHCOCH(alkyl)NH₂;
  • CH₂NHCOCH(CH₂0H)NH₂;
  • CH₂OCONH₂;
  • CH₂O(CH₂)₂NH₂;
  • CONHCH₃;
  • CONH₂;
  • CON(CH₃)₂;
  • CONH(CH₂)_nNH₂;
  • CONH(CH₂)_nNHCH₃;
  • CONH(CH₂)_nN(CH₃)₂; and
• n is 1, 2, or 3.

Definitions

As used herein, the term “alkenyl” refers to a straight or branched hydrocarbon of a designed number of carbon atoms containing at least one carbon-carbon double bond. Examples of “alkenyl” include vinyl, allyl, and 2-methyl-3-heptene.

The term “alkoxy” represents an alkyl attached to the parent molecular moiety through an oxygen bridge. Examples of alkoxy groups include, for example, methoxy, ethoxy, propoxy and isopropoxy.

The term “thioalkoxy” represents an alkyl attached to the parent molecular moiety through a sulfur atom. Examples of thioalkoxy groups include, for example, thiomethoxy, thioethoxy, thiopropoxy and thioisopropoxy.

As used herein, the term “alkyl” includes those alkyl groups of a designed number of carbon atoms. Alkyl groups may be straight or branched. Examples of “alkyl” include methyl, ethyl, propyl, isopropyl, butyl, iso-, sec- and tert-butyl, pentyl, hexyl, heptyl, 3-ethylbutyl, and the like. “Cx-Cy alkyl” represents an alkyl group of the specified number of carbons. For example, C₁-C₄ alkyl includes all alkyl groups that include at least one and no more than four carbon atoms. It also contains subgroups, such as, for example, C₂-C₃ alkyl or C₁-C₃ alkyl.

The term “aryl” refers to an aromatic hydrocarbon ring system containing at least one aromatic ring. The aromatic ring may optionally be fused or otherwise attached to other aromatic hydrocarbon rings or non-aromatic hydrocarbon rings. Examples of aryl groups include, for example, phenyl, naphthyl, 1,2,3,4-tetrahydronaphthalene, indanyl, and biphenyl. Preferred examples of aryl groups include phenyl and naphthyl. The most preferred aryl group is phenyl. The aryl groups herein are unsubstituted or, as specified, substituted in one or more substitutable positions with various groups. Thus, such aryl groups can be optionally substituted with groups such as, for example, C₁-C₆ alkyl, C₁-C₆ alkoxy, halogen, hydroxy, cyano, nitro, amino, mono- or di-(C₁-C₆)alkylamino, C₂-C₆alkenyl, C₂-C₆alkynyl, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy, amino(C₁-C₆)alkyl, mono- or di(C₁-C₆)alkylamino(C₁-C₆)alkyl.

The term “arylalkyl” refers to an aryl group, as defined above, attached to the parent molecular moiety through an alkyl group, as defined above. Preferred arylalkyl groups include, benzyl, phenethyl, phenpropyl, and phenbutyl. More preferred arylalkyl groups include benzyl and phenethyl. The most preferred arylalkyl group is benzyl. The aryl portions of these groups are unsubstituted or, as specified, substituted in one or more substitutable positions with various groups. Thus, such aryl groups can be optionally substituted with groups such as, for example, C₁-C₆ alkyl, C₁-C₆ alkoxy, halogen, hydroxy, cyano, nitro, amino, mono- or di-(C₁-C₆)alkylamino, C₂-C₆alkenyl, C₂-C₆alkynyl, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy, amino(C₁-C₆)alkyl, mono- or di(C₁-C₆)alkylamino(C₁-C₆)alkyl.

The term “arylalkoxy” refers to an aryl group, as defined above, attached to the parent molecular moiety through an alkoxy group, as defined above. Preferred arylaloxy groups include, benzyloxy, phenethyloxy, phenpropyloxy, and phenbutyloxy. The most preferred arylalkoxy group is benzyloxy.

The term “cycloalkyl” refers to a C₃-C₈ cyclic hydrocarbon. Examples of cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl. More preferred cycloalkyl groups include cyclopropyl.

The term “cycloalkylalkyl,” as used herein, refers to a C₃-C₈ cycloalkyl group attached to the parent molecular moiety through an alkyl group, as defined above. Examples of cycloalkylalkyl groups include cyclopropylmethyl and cyclopentylethyl.

The terms “halogen” or “halo” indicate fluorine, chlorine, bromine, or iodine.

The term “heterocycloalkyl,” refers to a non-aromatic ring system containing at least one heteroatom selected from nitrogen, oxygen, and sulfur, wherein the non-aromatic heterocycle is attached to the core. The heterocycloalkyl ring may be optionally fused to or otherwise attached to other heterocycloalkyl rings, aromatic heterocycles, aromatic hydrocarbons and/or non-aromatic hydrocarbon rings. Preferred heterocycloalkyl groups have from 3 to 7 members. Examples of heterocycloalkyl groups include, for example, piperazine, 1,2,3,4-tetrahydroisoquinoline, morpholine, piperidine, tetrahydrofuran, pyrrolidine, and pyrazole. Preferred heterocycloalkyl groups include piperidinyl, piperazinyl, morpholinyl, and pyrolidinyl. The heterocycloalkyl groups herein are unsubstituted or, as specified, substituted in one or more substitutable positions with various groups. Thus, such heterocycloalkyl groups can be optionally substituted with groups such as, for example, C₁-C₆ alkyl, C₁-C₆ alkoxy, halogen, hydroxy, cyano, nitro, amino, mono- or di-(C₁-C₆)alkylamino, C₂-C₆alkenyl, C₂-C₆alkynyl, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy, amino(C₁-C₆)alkyl, mono- or di(C₁-C₆)alkylamino(C₁-C₆)alkyl.

The term “heteroaryl” refers to an aromatic ring system containing at least one heteroatom selected from nitrogen, oxygen, and sulfur. The heteroaryl ring may be fused or otherwise attached to one or more heteroaryl rings, aromatic or non-aromatic hydrocarbon rings or heterocycloalkyl rings. Examples of heteroaryl groups include, for example, pyridine, furan, thiophene, 5,6,7,8-tetrahydroisoquinoline and pyrimidine. Preferred examples of heteroaryl groups include thienyl, benzothienyl, pyridyl, quinolyl, pyrazinyl, pyrimidyl, imidazolyl, benzimidazolyl, furanyl, benzofuranyl, thiazolyl, benzothiazolyl, isoxazolyl, oxadiazolyl, isothiazolyl, benzisothiazolyl, triazolyl, tetrazolyl, pyrrolyl, indolyl, pyrazolyl, and benzopyrazolyl. Preferred heteroaryl groups include pyridyl. The heteroaryl groups herein are unsubstituted or, as specified, substituted in one or more substitutable positions with various groups. Thus, such heteroaryl groups can be optionally substituted with groups such as, for example, C₁-C₆ alkyl, C₁-C₆ alkoxy, halogen, hydroxy, cyano, nitro, amino, mono- or di-(C₁-C₆)alkylamino, C₂-C₆alkenyl, C₂-C₆alkynyl, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy, amino(C₁-C₆)alkyl, mono- or di(C₁-C₆)alkylamino(C₁-C₆)alkyl.

The term “heteroarylalkyl” refers to a heteroaryl group, as defined above, attached to the parent molecular moiety through an alkyl group, as defined above. Preferred heteroarylalkyl groups include, pyrazolemethyl, pyrazoleethyl, pyridylmethyl, pyridylethyl, thiazolemethyl, thiazoleethyl, imidazolemethyl, imidazoleethyl, thienylmethyl, thienylethyl, furanylmethyl, furanylethyl, isoxazolemethyl; isoxazoleethyl, pyrazinemethyl and pyrazineethyl. More preferred heteroarylalkyl groups include pyridylmethyl and pyridylethyl. The heteroaryl portions of these groups are unsubstituted or, as specified, substituted in one or more substitutable positions with various groups. Thus, such heteroaryl groups can be optionally substituted with groups such as, for example, C₁-C₆ alkyl, C₁-C₆ alkoxy, halogen, hydroxy, cyano, nitro, amino, mono- or di-(C₁-C₆)alkylamino, C₂-C₆alkenyl, C₂-C₆alkynyl, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy, amino(C₁-C₆)alkyl, mono- or di(C₁-C₆)alkylamino(C₁-C₆)alkyl.

If two or more of the same substituents are on a common atom, e.g., di(C₁-C₆)alkylaamino, it is understood that the nature of each group is independent of the other.

As used herein, the term “p38 mediated disorder” refers to any and all disorders and disease states in which p38 plays a role, either by control of p38 itself, or by p38 causing another factor to be released, such as but not limited to IL-1, IL-6 or IL-8. A disease state in which, for instance, IL-1 is a major component, and whose production or action, is exacerbated or secreted in response to p38, would therefore be considered a disorder mediated by p38.

With reference to the use of the words “comprise” or “comprises” or “comprising” in this patent (including the claims), Applicants note that unless the context requires otherwise, those words are to be interpreted inclusively rather than exclusively.

As TNF-beta has close structural homology with TNF-alpha (also known as cachectin), and since each induces similar biologic responses and binds to the same cellular receptor, the synthesis of both TNF-alpha and TNF-beta are inhibited by the compounds of the present invention and thus are herein referred to collectively as “TNF” unless specifically delineated otherwise.

Non-toxic pharmaceutically acceptable salts include, but are not limited to salts of inorganic acids such as hydrochloric, sulfuric, phosphoric, diphosphoric, hydrobromic, and nitric or salts of organic acids such as formic, citric, malic, maleic, fumaric, tartaric, succinic, acetic, lactic, methanesulfonic, p-toluenesulfonic, 2-hydroxyethylsulfonic, salicylic and stearic. Similarly, pharmaceutically acceptable cations include, but are not limited to sodium, potassium, calcium, aluminum, lithium and ammonium. Those skilled in the art will recognize a wide variety of non-toxic pharmaceutically acceptable addition salts.

The compounds of this invention may contain one or more asymmetric carbon atoms, so that the compounds can exist in different stereoisomeric forms. These compounds can be, for example, racemates, chiral non-racemic or diastereomers. In these situations, the single enantiomers, i.e., optically active forms, can be obtained by asymmetric synthesis or by resolution of the racemates. Resolution of the racemates can be accomplished, for example, by conventional methods such as crystallization in the presence of a resolving agent; chromatography, using, for example a chiral HPLC column; or derivatizing the racemic mixture with a resolving reagent to generate diastereomers, separating the diastereomers via chromatography or selective crystallization, and removing the resolving agent to generate the original compound in enantiomerically enriched form. Any of the above procedures can be repeated to increase the enantiomeric purity of a compound.

The compounds of the invention may exist as atropisomers, i.e., chiral rotational isomers. The invention encompasses the racemic and the resolved atropisomers. The following illustration generically shows a compound (Z) that can exist as atropisomers as well as its two possible atropisomers (A) and (B). This illustration also shows each of atropisomers (A) and (B) in a Fischer projection. In this illustration, R₁, R₂, and R₄ carry the same definitions as set forth for Formula I, R_p′ is a substituent within the definition of R₅, and R_p is a non-hydrogen substituent within the definition of R₅.

When the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry, and unless otherwise specified, it is intended that the compounds include the cis, trans, Z- and E-configurations. Likewise, all tautomeric forms are also intended to be included.

The compounds of general Formula I may be administered orally, topically, parenterally, by inhalation or spray or rectally in dosage unit formulations containing conventional non-toxic pharmaceutically acceptable carriers, adjuvants and vehicles. The term parenteral as used herein includes percutaneous, subcutaneous, intravascular (e.g., intravenous), intramuscular, or intrathecal injection or infusion techniques and the like. In addition, there is provided a pharmaceutical formulation comprising a compound of general Formula I and a pharmaceutically acceptable carrier. One or more compounds of general Formula I may be present in association with one or more non-toxic pharmaceutically acceptable carriers and/or diluents and/or adjuvants, and if desired other active ingredients. The pharmaceutical compositions containing compounds of general Formula I may be in a form suitable for oral use, for example, as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsion, hard or soft capsules, or syrups or elixirs.

For oral administration, the pharmaceutical composition may be in the form of, for example, a tablet, hard or soft capsule, lozenges, dispensable powders, suspension, or liquid. The pharmaceutical composition is preferably made in the form of a dosage unit containing a particular amount of the active ingredient. Examples of such dosage units are tablets or capsules.

Compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions and such compositions may contain one or more agents selected from the group consisting of sweetening agents, flavoring agents, coloring agents and preservative agents in order to provide pharmaceutically elegant and palatable preparations. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients that are suitable for the manufacture of tablets. These excipients may be for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid; binding agents, for example starch, gelatin or acacia, and lubricating agents, for example magnesium stearate, stearic acid or talc. The tablets may be uncoated or they may be coated by known techniques. In some cases such coatings may be prepared by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time delay material such as glyceryl monosterate or glyceryl distearate may be employed.

Formulations for oral use may also be presented as hard gelatin capsules, wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate, or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin or olive oil.

Formulations for oral use may also be presented as lozenges.

Aqueous suspensions contain the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions. Such excipients are suspending agents, for example sodium carboxymethylcellulose, methylcellulose, hydropropyl-methylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally-occurring phosphatide, for example, lecithin, or condensation products of an alkylene oxide with fatty acids, for example polyoxyethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives, for example ethyl, or n-propyl p-hydroxybenzoate, one or more coloring agents, one or more flavoring agents, and one or more sweetening agents, such as sucrose or saccharin.

Oily suspensions may be formulated by suspending the active ingredients in a vegetable oil, for example arachis oil, olive oil, sesame oil, or coconut oil, or in a mineral oil such as liquid paraffin. The oily suspensions may contain a thickening agent, for example beeswax, hard paraffin, or cetyl alcohol. Sweetening agents and flavoring agents may be added to provide palatable oral preparations. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.

Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water provide the active ingredient in admixture with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents or suspending agents are exemplified by those already mentioned above. Additional excipients, for example sweetening, flavoring, and coloring agents, may also be present.

Pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil or a mineral oil or mixtures of these. Suitable emulsifying agents may be naturally-occurring gums, for example gum acacia or gum tragacanth, naturally-occurring phosphatides, for example soy bean, lecithin, and esters or partial esters derived from fatty acids and hexitol, anhydrides, for example sorbitan monooleate, and condensation products of the said partial esters with ethylene oxide, for example polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening and flavoring agents.

Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol, sorbitol, glucose or sucrose. Such formulations may also contain a demulcent, a preservative, and flavoring and coloring agents. The pharmaceutical compositions may be in the form of a sterile injectable aqueous or oleaginous suspension. This suspension may be formulated according to the known art using those suitable dispersing or wetting agents and suspending agents that have been mentioned above. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parentally acceptable diluent or solvent, for example as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono-or diglycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables.

The compounds of general Formula I may also be administered in the form of suppositories, e.g., for rectal administration of the drug. These compositions can be prepared by mixing the drug with a suitable non-irritating excipient that is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug. Such materials include cocoa butter and polyethylene glycols.

Compounds of general Formula I may be administered parenterally in a sterile medium. The drug, depending on the vehicle and concentration used, can either be suspended or dissolved in the vehicle. Advantageously, adjuvants such as local anesthetics, preservatives, and buffering agents can be dissolved in the vehicle.

The active ingredient may also be administered by injection (IV, IM, subcutaneous or jet) as a composition wherein, for example, saline, dextrose, or water may be used as a suitable carrier. The pH of the composition may be adjusted, if necessary, with suitable acid, base, or buffer. Suitable bulking, dispersing, wetting or suspending agents, including mannitol and PEG 400, may also be included in the composition. A suitable parenteral composition can also include a compound formulated as a sterile solid substance, including lyophilized powder, in injection vials. Aqueous solution can be added to dissolve the compound prior to injection.

For disorders of the eye or other external tissues, e.g., mouth and skin, the formulations are preferably applied as a topical gel, spray, ointment or cream, or as a suppository, containing the active ingredients in a total amount of, for example, 0.075 to 30% w/w, preferably 0.2 to 20% w/w and most preferably 0.4 to 15% w/w. When formulated in an ointment, the active ingredients may be employed with either paraffinic or a water-miscible ointment base.

Alternatively, the active ingredients may be formulated in a cream with an oil-in-water cream base. If desired, the aqueous phase of the cream base may include, for example at least 30% w/w of a polyhydric alcohol such as propylene glycol, butane-1,3-diol, mannitol, sorbitol, glycerol, polyethylene glycol and mixtures thereof. The topical formulation may desirably include a compound, which enhances absorption or penetration of the active ingredient through the skin or other affected areas. Examples of such dermal penetration enhancers include dimethylsulfoxide and related analogs. The compounds of this invention can also be administered by a transdermal device. Preferably topical administration will be accomplished using a patch either of the reservoir and porous membrane type or of a solid matrix variety. In either case, the active agent is delivered continuously from the reservoir or microcapsules through a membrane into the active agent permeable adhesive, which is in contact with the skin or mucosa of the recipient. If the active agent is absorbed through the skin, a controlled and predetermined flow of the active agent is administered to the recipient. In the case of microcapsules, the encapsulating agent may also function as the membrane. The transdermal patch may include the compound in a suitable solvent system with an adhesive system, such as an acrylic emulsion, and a polyester patch. The oily phase of the emulsions of this invention may be constituted from known ingredients in a known manner. While the phase may comprise merely an emulsifier, it may comprise a mixture of at least one emulsifier with a fat or oil or with both a fat and an oil. Preferably, a hydrophilic emulsifier is included together with a lipophilic emulsifier, which acts as a stabilizer. It is also preferred to include both an oil and a fat. Together, the emulsifier(s) with or without stabilizer(s) make-up the so-called emulsifying wax, and the wax together with the oil and fat make up the so-called emulsifying ointment base, which forms the oily, dispersed phase of the cream formulations. Emulsifiers and emulsion stabilizers suitable for use in the formulation of the present invention include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl monostearate, and sodium lauryl sulfate, among others. The choice of suitable oils or fats for the formulation is based on achieving the desired cosmetic properties, since the solubility of the active compound in most oils likely to be used in pharmaceutical emulsion formulations is very low. Thus, the cream should preferably be a non-greasy, non-staining and washable product with suitable consistency to avoid leakage from tubes or other containers. Straight or branched chain, mono- or dibasic alkyl esters such as di-isoadipate, isocetyl stearate, propylene glycol diester of coconut fatty acids, isopropyl myristate, decyl oleate, isopropyl palmitate, butyl stearate, 2-ethylhexyl palmitate or a blend of branched chain esters may be used. These may be used alone or in combination depending on the properties required. Alternatively, high melting point lipids such as white soft paraffin and/or liquid paraffin or other mineral oils can be used.

Formulations suitable for topical administration to the eye also include eye drops wherein the active ingredients are dissolved or suspended in suitable carrier, especially an aqueous solvent for the active ingredients. The anti-inflammatory active ingredients are preferably present in such formulations in a concentration of 0.5 to 20%, advantageously 0.5 to 10% and particularly about 1.5% w/w. For therapeutic purposes, the active compounds of this combination invention are ordinarily combined with one or more adjuvants appropriate to the indicated route of administration. If administered per os, the compounds may be admixed with lactose, sucrose, starch powder, cellulose esters of alkanoic acids, cellulose alkyl esters, talc, stearic acid, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphoric and sulfuric acids, gelatin, acacia gum, sodium alginate, polyvinylpyrrolidone, and/or polyvinyl alcohol, and then tableted or encapsulated for convenient administration. Such capsules or tablets may contain a controlled-release formulation as may be provided in a dispersion of active compound in hydroxypropylmethyl cellulose. Formulations for parenteral administration may be in the form of aqueous or non-aqueous isotonic sterile injection solutions or suspensions. These solutions and suspensions may be prepared from sterile powders or granules having one or more of the carriers or diluents mentioned for use in the formulations for oral administration. The compounds may be dissolved in water, polyethylene glycol, propylene glycol, ethanol, corn oil, cottonseed oil, peanut oil, sesame oil, benzyl alcohol, sodium chloride, and/or various buffers. Other adjuvants and modes of administration are well and widely known in the pharmaceutical art.

The amount of therapeutically active compounds that are administered and the dosage regimen for treating a disease condition with the compounds and/or compositions of this invention depends on a variety of factors, including the age, weight, sex and medical condition of the subject, the severity of the inflammation or inflammation related disorder, the route and frequency of administration, and the particular compound employed, and thus may vary widely. The pharmaceutical compositions may contain active ingredients in the range of about 0.1 to 1000 mg, preferably in the range of about 7.0 to 350 mg. A daily dose of about 0.01 to 100 mg/kg body weight, preferably between about 0.1 and about 50 mg/kg body weight and most preferably between about 0.5 to 30 mg/kg body weight, may be appropriate. The daily dose can be administered in one to four doses per day. In the case of skin conditions, it may be preferable to apply a topical preparation of compounds of this invention to the affected area two to four times a day.

It will be understood, however, that the specific dose level for any particular patient will depend upon a variety of factors including the activity of the specific compound employed, the age, body weight, general health, sex, diet, time of administration, route of administration, and rate of excretion, drug combination and the severity of the particular disease undergoing therapy.

For administration to non-human animals, the composition may also be added to the animal feed or drinking water. It may be convenient to formulate the animal feed and drinking water compositions so that the animal takes in a therapeutically appropriate quantity of the composition along with its diet. It may also be convenient to present the composition as a premix for addition to the feed or drinking water.

The disclosures in this application of all articles and references, including patents, are incorporated herein by reference.

The invention is illustrated further by the following examples, which are not to be construed as limiting the invention in scope or spirit to the specific procedures described in them.

The starting materials and various intermediates may be obtained from commercial sources, prepared from commercially available compounds, or prepared using well-known synthetic methods.

The compound names in this application were created using ACD Name Pro version 5.09, or ChemDraw ultra version 6.0.2, software.

General Synthetic Procedures

Representative procedures for the preparation of compounds of the invention are outlined below in the Schemes The starting materials can be purchased or prepared using methods known to those skilled in the art. Similarly, the preparation of the various intermediates can be achieved using methods known in the art. The starting materials may be varied and additional steps employed to produce compounds encompassed by the invention, as demonstrated by the examples below. In addition, different solvents and reagents can typically be used to achieve the above transformations. Protection of reactive groups may also be necessary to achieve the above transformations. In general, the need for protecting groups, as well as the conditions necessary to attach and remove such groups, will be apparent to those skilled in the art of organic synthesis. When a protecting group is employed, deprotection will generally be required. Suitable protecting groups and methodology for protection and deprotection such as those described in Protecting Groups in Organic Synthesis by Greene and Wuts are known and appreciated in the art.

In this scheme, R₅ is as defined above.

Alternatively, the compounds of the instant invention can be prepared according to the method outlined in Scheme 2.

Q at each occurrence is independently alkyl, halogen, alkoxy, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO₂H, CN, amidinooxime, NR₆R₇, NR₆R₇alkyl, —C(O)NR₆R₇, amidino, haloalkyl, or haloalkoxy; and n is 0, 1, 2, 3, 4, or 5.

Alternatively, compounds of the invention can be prepared using the procedures outlined in Schemes 3-30. Q is as above.

Y at each occurrence is independently alkyl, halogen, alkoxy, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO₂H, CN, amidinooxime, NR₆R₇, R₆R₇N(C₁-C₆)alkyl, —C(O)NR₆R₇, (C₁-C₄)alkyl-C(O)NR₆R₇, amidino, haloalkyl, or haloalkoxy; and n is 0, 1, 2, 3, 4, or 5.

R is aryl, alkyl, heteroaryl, arylalkyl heteroarylalkyl, heterocycloalkyl, or heterocycloalkylalkyl. R may be unsubstituted or substituted with Y.

R′ is aryl, alkyl, heteroaryl, arylalkyl heteroarylalkyl, heterocycloalkyl, or heterocycloalkylalkyl. R may be unsubstituted or substituted with Q.

X is Br or Cl.

EXAMPLES

The invention is illustrated further by the following examples, which are not to be construed as limiting the invention in scope or spirit to the specific procedures described in them. Those having skill in the art will recognize that the starting materials may be varied and additional steps employed to produce compounds encompassed by the invention, as demonstrated by the following examples. Those skilled in the art will also recognize that it may be necessary to utilize different solvents or reagents to achieve some of the above transformations. In some cases, protection of reactive functionalities may be necessary to achieve the above transformations. In general, such need for protecting groups, as well as the conditions necessary to attach and remove such groups, will be apparent to those skilled in the art of organic synthesis. When a protecting group is employed, a deprotection step may be required. Suitable protecting groups and methodology for protection and deprotection such as those described in Protecting Groups in Organic Synthesis by Greene and Wuts are well known and appreciated in the art.

Unless otherwise specified, all reagents and solvents are of standard commercial grade and are used without further purification. The appropriate atmosphere to run the reaction under, for example, air, nitrogen, hydrogen, argon and the like, will be apparent to those skilled in the art.

Example 1

Preparation of 4-(benzyloxy)-1-(4-methylbenzyl)pyridin-2(1H)-one

4-Benzyloxy-2(1H)-pyridone (3.0 g, 0.015 mol), 4-methylbenzyl bromide (3.15 g, 0.17 mol), and potassium carbonate (3.0 g, 0.022 mol) were heated at 80° C. for 2 hours. Contents were allowed to cool, diluted with water and a solid (5.52 g) was filtered. FABHRMS m/z 306.1494 (M+H, C₂₀H₂₀NO₂ requires 306.1494). ¹H NMR (CDCl₃/300 MHz): 7.50-7.40 (m, 5H); 7.20-7.05 (m, 5H); 6.07-6.00 (m, 1H); 5.95-5.90 (m, 1H); 5.05 (s, 2H); 5.00 (s, 2H); 2.32 (s, 3H). Anal. Calcd for C₂₀H₁₉NO₂: C, 78.66; H, 6.27; N, 4.59. Found: C, 78.54; H, 6.38; N, 4.58.

Example 2

Preparation of 4-(benzyloxy)-3-bromo-1-(4-methylbenzyl)pyridin-2(1H)-one

The material prepared in Example 1(2.1 g, 0.007 mol) and sodium acetate (738 mg, 0.009 mol) in glacial acetic acid (15 mL) were cooled to 15° C. Bromine (0.412 mL, 0.008) in glacial acetic acid (5 mL) was added dropwise. Contents were stirred 2 hours, coming to room temperature. Water (200 mL) was added and a light yellow solid was filtered. Mp 150.4-151.2° C. FABHRMS m/z 384.0599 (M+H, C₂₀H₁₉BrNO₂ requires 384.0601). ¹H NMR (CDCl₃/300 MHz) δ: 7.42-7.30 (m, 5H); 7.22-7.08 (m, 5H); 6.02 (d, 1H); 5.20 (s, 2H); 5.12 (s, 2H); 2.32 (s, 3H). Anal. Calcd for C₂₀H₁₈BrNO₂: C, 62.51; H, 4.72; N, 3.65. Found: C, 62.11; H, 4.48; N, 3.54.

Examples 3-10

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 3-10 are prepared essentially according to the procedure set forth above with respect to Example 1. Compounds wherein R₁=Br are prepared essentially according to the procedure of Example 2.

Example				M + H m/z	FABHRMS
No.	R1	R2	MF	Requires	m/z
Ex. 3	—H	4-Br	C19H16BrNO2	370.0428	370.0443
Ex. 4	—Br	4-Br	C19H15Br2NO2	447.9522	447.9548
Ex. 5	—H	4-Cl	C19H16ClNO2	326.0948	326.0893
Ex. 6	—Br	4-Cl	C19H15BrClNO2	404.0053	404.0035
Ex. 7	—H	3-F	C19H16FNO2	310.1243	310.1226
Ex. 8	—Br	3-F	C19H15BrFNO2
Ex. 9	—H	2-F	C19H16FNO2	310.1231	310.1243
Ex. 10	—Br	2-F	C19H15BrFNO2	388.0348	388.0373

NMR characterization of compounds of Examples 3-10

Ex. No. NMR Data
Ex. 3   1H NMR (CDCl3/300 MHz) δ: 7.43(d, 2H); 7.40-7.33(m, 5H); 7.20-7.07(m, 3H); 6.04-
        6.01(m, 1H); 6.00-5.92(m, 1H); 5.03(s, 2H); 4.98(s, 2H)
Ex. 4   1H NMR (CDCl3/300 MHz) δ: 7.50-7.15(m, 10H); 6.06(d, 1H); 5.20(s, 2H), 5.10(s, 2H)
Ex. 5   1H NMR (CDCl3/300 MHz) δ: 7.40-7.32(m, 5H); 7.24(AB quartet, 4H); 7.10(d, 1H); 6.03-
        6.00(m, 1H); 5.98-5.92(m, 1H); 5.03(s, 2H); 4.99(s, 2H)
Ex. 6   1H NMR (CDCl3/300 MHz): 7.43-7.20(m, 10H); 6.08(d, 1H); 5.20(s, 2H); 5.10(s, 2H)
Ex. 7   1H NMR (CDCl3/300 MHz) δ: 7.45-7.25(m, 5H); 7.12(d, 1H); 7.07-6.93(m, 4H); 6.04-
        6.02(m, 1H); 6.00-5.94(m, 1H); 5.08(s, 2H); 5.00(s, 2H)
Ex. 8   1H NMR (CDCl3/300 MHz) δ: 7.43-7.25(m, 6H); 7.21(d, 1H); 7.10-6.93(m, 3H); 6.08(d,
        1H); 5.22(s, 2H); 5.12(s, 2H)
Ex. 9   1H NMR (CDCl3/300 MHz) δ: 7.43-7.00(m, 10H); 6.01-5.92(m, 2H); 5.10(s, 2H); 4.99(s,
        2H)
Ex. 10  1H NMR (CDCl3/300 MHz): 7.52(d of t, 1H); 7.44-7.26(m, 7H); 7.15-7.00(m, 2H); 6.03
        (d, 1H); 5.20(s, 2H); 5.15(s, 2H)

Example 11

Preparation of 4-(benzyloxy)-3-bromopyridin-2(1H)-one

The material of Example 11 was prepared according to the procedure of Example 2. ¹H NMR (CDCl₃/300 MHz) δ: 7.50-7.30 (m, 6H); 6.20 (d, 1H); 5.24 (s, 2H). Anal. Calcd for C₁₂H₁₀BrNO₂ (0.3H₂0): C, 50.48; H, 3.74; N, 4.91. Found: C, 50.79; H, 3.41; N, 4.82.

Examples 12-19

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 12-19 are prepared essentially according to the procedures set forth above for Example 1. Compounds wherein R₁=Br are prepared essentially according to the procedure of Example 2.

Example				M + H	FABHRMS
No.	R1	R2	MF	Requires	m/z
Ex. 12	—Br	4-benzyl-	C26H22BrNO3	476.0861	476.0854
		oxy
Ex. 13	—H	4-CO2Me	C21H19NO4	350.1392	350.1391
Ex. 14	—Br	4-CO2Me	C21H18BrNO4	428.0497	428.0480
Ex. 15	—Br	4-CO2H	C20H16BrNO4	414.0341	414.0360
Ex. 16	—H	4-CN	C20H16N2O2	317.1290	317.1270
Ex. 17	—Br	4-CN	C20H15BrN2O2	395.0395	395.0376
Ex. 18	—H	4-tButyl	C23H25NO2	348.1964	348.1949
Ex. 19	—Br	4-tButyl	C23H24BrNO2	426.1069	426.1023

NMR characterization of compounds of Examples 12-19

Ex. No. NMR Data
Ex. 12  1H NMR (CDCl3/300 MHz): 7.45-7.15(m, 13H); 6.92(d, 2H); 6.01(d, 1H); 5.20(s, 2H);
        5.08(s, 2H); 5.03(s, 2H)
Ex. 13  1H NMR (CDCl3/300 MHz): 8.00(d, 2H); 7.40-7.25(m, 7H); 7.10(d, 1H); 6.03-6.01(m,
        1H); 6.00-5.93(m, 1H); 5.12,(s, 2H); 5.00(s, 2H); 3.95(s, 3H)
Ex. 14  1H NMR (CDCl3/300 MHz): 8.00(d, 2H); 7.42-7.31(m, 7H); 7.23(d, 1H); 6.08(d, 1H);
        5.22(d, 2H); 5.20(s, 2H); 3.95(s, 3H)
Ex. 15  1H NMR (DMSO-d6/300 MHz): 8.00-7.80(m, 3H); 7.53-7.27(m, 7H); 6.50(d, 1H); 5.32
        (s, 2H); 5.20(s, 2H)
Ex. 16  1H NMR (CDCl3/300 MHz) δ: 7.60(d, 2H); 7.42-7.30(m, 7H); 7.13(d, 1H); 6.05-5.98(m,
        2H); 5.11(s, 2H); 5.00(s, 2H)
Ex. 17  1H NMR (CDCl3/300 MHz) δ: 7.61(d, 2H); 7.48-7.30(m, 6H); 7.23(d, 2H); 6.12(d, 1H);
        5.22(s, 2H); 5.20(s, 2H)
Ex. 18  1H NMR (CDCl3/300 MHz): 7.40-7.28(m, 7H); 7.20(d, 2H); 7.10(d, 1H); 6.02(d, 1H);
        5.97-5.90(m, 1H); 5.02(d, 2H); 4.98(d, 2H)
Ex. 19  1H NMR (CDCl3/300 MHz) δ: 7.43-7.20(m, 10H); 6.02(d, 1H); 5.20(s, 2H); 5.10(s, 2H);
        1.30(s, 9H)

Example 20

Preparation of 4-(benzyloxy)-3-bromo-1-ethylpyridin-2(1H)-one

To 4-benzyloxy-2(1H)-pyridone (1.0 g, 0.005 mol) and potassium carbonate (1.0 g, 0.007 mol) in DMF (10 mL) was added bromoethane (0.82 mL, 0.011 mol). Contents were heated at 75° C. overnight. Contents were allowed to cool and partitioned between EtOAc and water. The EtOAc layer was dried over MgSO₄, filtered, and concentrated in vacuo leaving a waxy solid, which was recrystallized from EtOAc/hexanes to give a white solid (720 mg). To the white solid (700 mg, 0.003 mol) in glacial acetic acid (10 mL), bromine (0.17 mL, 0.00325 mol) in glacial acetic acid (5 mL) was added dropwise at 15° C. Contents were stirred one hour at room temperature and a yellow solid (1.1 g) was filtered. The solid was partitioned between EtOAc and 2.5N sodium hydroxide. The EtOAc layer was dried over MgSO₄, filtered, and concentrated in vacuo leaving a colorless oil (710 mg), which solidified. FABHRMS m/z 310.0267 (M+H, C₁₄H₁₅BrNO₂ requires 310.0263). ¹H NMR (CDCl₃/300 MHz) δ: 7.45-7.30 (m, 6H); 7.22 (d, 1H); 6.07 (d, 1H); 5.20 (s, 2H); 4.00 (q, 2H); 1.32 (t, 3H). Anal. Calcd for C₁₄H₁₄BrNO₂: C, 54.56; H, 4.58; N, 4.55. Found: C, 54.21; H, 4.38; N, 4.43.

Example 21

Preparation of 3-bromo-4-hydroxy-1-(4-hydroxybenzyl)pyridin-2(1H)-one

The material of Example 12 (120 mg, 0.25 mmol) and 10% palladium/carbon (30 mg) in glacial acetic acid (2 mL) were shaken at 55 lbs of hydrogen for 4 hours. Contents were filtered and the filtrate was concentrated in vacuo leaving an oil. FABHRMS m/z 295.9952 (M+H, C₁₂H₁₁BrNO₃ requires 295.9922). ¹H NMR (DMSO-d₆/300 MHz) δ: 11.40 (br s, 1H); 9.40 (br s, 1H); 7.60 (d, 1H); 7.10 (d, 2H); 6.70 (d, 2H); 6.02 (d, 1H); 4.93 (s, 2H). Anal. Calcd for C₁₂H₁₀BrNO₃ (1.4 H₂O): C, 44.85; H, 4.02; N, 4.36. Found: C, 45.07; H, 4.10; N, 4.35.

Example 22

Prepararation of 4-(benzyloxy)-3-bromo-1-methylpyridin-2(1H)-one Hydrobromide

To 4-benzyloxy-2(1H)-pyridone (1.0 g, 0.005 mol) and potassium carbonate (760 mg, 0.0055 mol) in DMF (10 mL) was added methyl iodide (0.342 mL, 0.0055 mol). Contents were stirred overnight. Contents were partitioned between EtOAc and water. The EtOAc layer was dried over MgSO₄, filtered, and concentrated in vacuo leaving a white solid (960 mg). To the white solid (332 mg, 0.0015 mol) in glacial acetic acid (10 mL), bromine (256 mg, 0.0016 mol) in glacial acetic acid (5 mL) was added dropwise at 15° C. Contents were stirred one hour at room temperature and the desired was filtered as a white solid, 262 mg (59% yield). mp 105.3-105.6° C. FABHRMS m/z 296.0097 (M+H, C₁₃H₁₃BrNO₂ requires 296.0110). ¹H NMR (CDCl₃/300 MHz) δ: 7.45-7.30 (m, 6H); 7.22 (d, 1H); 6.07 (d, 1H); 5.20 (s, 2H); 4.00 (q, 2H); 1.32 (t, 3H). Anal. Calcd for C₁₃H₁₂BrNO₂ (HBr, 0.3H₂O): C, 41.04; H, 3.60; N, 3.68. Found: C, 41.00; H, 3.87; N, 3.52.

Example 23

Prepararation of 4-(benzyloxy)-3-bromo-1-methylpyridin-2(1H)-one

The material of Example 22 was partitioned between EtOAc and 2.5N sodium hydroxide. The EtOAc layer was dried over MgSO₄, filtered, and concentrated in vacuo leaving a red oil, which solidified. FABHRMS m/z 294.0112 (M+H, C₁₃H₁₃BrNO₂ requires 294.0130). ¹H NMR (CDCl₃/300 MHz): 7.45-7.30 (m, 6H); 7.22 (d, 1H); 6.07 (d, 1H); 5.20 (s, 2H); 4.00 (q, 2H); 1.32 (t, 3H). Anal. Calcd for C₁₃H₁₂BrNO₂: C, 53.08; H, 4.11; N, 4.76. Found: C, 53.06; H, 4.20; N, 4.74.

Example 24

Preparation of 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}-N′-hydroxybenzenecarboximidamide

The material of Example 17 (500 mg, 0.00127 mol), hydroxylamine hydrochloride (90 mg, 0.0013 mol) and sodium bicarbonate (109 mg) were refluxed in ethanol (15 mL) overnight. Contents were allowed to cool and a solid was filtered and washed with water to give the desired as a white solid, 447 mg, (82% yield). mp 210.2-212.2° C. FABHRMS m/z 428.0634 (M+H, C₂₀H₁₉BrN₃O₃ requires 428.0610). ¹H NMR (DMSO-d₆/300 MHz): 9.66 (s, 1H); 7.98 (d, 1H); 7.65 (d, 2H); 7.55-7.35 (m, 5H); 7.30 (d, 2H); 6.54 (d, 1H); 5.82 (s, 2H); 5.35 (s, 2H); 5.17 (s, 2H). Anal. Calcd for C₂₀H₁₈BrN₃O₃: C, 56.09; H, 4.24; N, 9.81. Found: C, 55.92; H, 4.01; N, 9.52.

Example 25

Preparation of 4-(benzyloxy)-3-bromo-1-(piperidin-4-ylmethyl)pyridin-2(1H)-one Hydrochloride

To the material of Example 11 (924 mg, 0.0033 mol) in DMF (5 mL) was added dropwise sodium bis(trimethylsilyl)amide (1M in THF, 3.6 mL). Contents were stirred one hour before adding dropwise a solution of 4-methanesulfonyloxymethyl-1-piperidine-1-carboxylic acid tert-butyl ester (J. Labelled Compd, Radiopharm, 38(7), 1996, 595-606) (1.0 g, 0.0036 mol) in DMF (5 mL). Contents were heated at 75° C. overnight. Contents were allowed to cool and poured into water (100 mL). A solid was filtered and recrystallized from EtOAc to give white crystals (546 mg). The white crystals were refluxed in 4 N HCl/dioxane (10 mL) for 3 hours, allowed to cool and filtered to give the desired as a white solid, 415 mg (30% yield). mp 207.9° C. FABHRMS m/z 377.0852 (M+H, C₁₈H₂₃BrClN₂O₂ requires 377.0865). ¹H NMR (DMSO-d₆/300 MHz) δ: 8.90 (br, 1H); 8.64 (br, 1H); 7.80 (d, 1H); 7.50-7.30 (m, 5H); 6.48 (d, 1H); 5.30 (s, 2H); 3.83 (d, 2H); 3.20 (d, 2H); 2.88-2.64 (m, 2H); 2.10-1.90 (m, 1H); 1.60 (d, 2H); 1.50-1.40 (m, 2H). Anal. Calcd for C₁₈H₂₂BrClN₂O₂ (0.3 H₂O): C, 51.58; H, 5.43; N, 6.68. Found: C, 51.59; H, 5.42; N, 6.81.

Example 26

Preparation of 4-(benzyloxy)-1-[4-(trifluoromethyl)benzyl]pyridin-2(1H)-one

The material of Example 26 was prepared according to the procedure of Example 1. FABHRMS m/z 360.1213 (M+H, C₂₀H₁₇F₃NO₂ requires 360.1211). ¹H NMR (CDCl₃/300 MHz) δ: 7.60 (d, 2H); 7.41-7.30 (m, 7H); 7.13 (d, 1H); 6.05-6.01 (m, 1H); 6.00-5.95 (m, 1H); 5.13 (s, 2H); 5.00 (s, 2H). Anal. Calcd for C₂₀H₁₆F₃NO₂: C, 66.85; H, 4.49; N, 3.90. Found: C, 66.64; H, 4.26; N, 3.93.

Example 27

Preparation of 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethyl) benzyl]pyridin-2(1H)-one

The material of Example 27 was prepared according to the procedure of Example 2. FABHRMS m/z 438.0308 (M+H, C₂₀H₁₆BrF₃NO₂ requires 438.0316). ¹H NMR (CDCl₃/300 MHz) δ: 7.65-7.20 (m, 10H); 6.13-6.03 (m, 1H); 5.30-5.13 (m, 4H). Anal. Calcd for C₂₀H₁₅BrF₃NO₂: C, 54.81; H, 3.45; N, 3.20. Found: C, 54.69; H, 3.34; N, 3.19.

Example 28

Preparation of 4-(benzyloxy)-3-bromo-1-(piperidin-3-ylmethyl)pyridin-2(1H)-one Hydrochloride

To the material of Example 11 (3.1 g, 0.011 mol) in DMF (20 mL) was added dropwise sodium bis(trimethylsilyl)amide (1M in THF, 12 mL). Contents were stirred one hour before adding dropwise a solution of 3-methanesulfonyloxymethyl-1-piperidine-1-carboxylic acid tert-butyl ester (Bioorg. Med. Chem. Lett, 8(13), 1998, 1595-1600) (4.2 g, 0.015 mol) in DMF (5 mL). Contents were heated at 75° C. overnight. Contents were allowed to cool, poured into water (100 mL) and a solid was filtered. The solid was stirred in 4 N HCl/dioxane (15 mL) for 3 hours and filtered to give the desired as a white solid, 752 mg (18% yield). mp 138.1-139.2° C. FABHRMS m/z 377.0859 (M+H, C₁₈H₂₂BrN₂O₂ requires 377.0865). ¹H NMR (DMSO-d₆/300 MHz): 9.50-9.10 (br, 2H); 8.00 (d, 1H); 7.50-7.30 (m, 5H); 6.93 (d, 1H); 5.30 (s, 2H); 4.30-3.90 (m, 3H); 3.40-3.10 (m, 3H); 2.80-2.50 (m, 3H); 2.40-2.00 (m, 1H); 1.90-1.60 (m, 4H); 1.40-1.10 (m, 1H). Anal. Calcd for C₁₈H₂₁BrN₂O₂ (2HCl, 0.25 H₂O): C, 47.55; H, 5.21; N, 6.16. Found: C, 47.48; H, 5.46; N, 6.27.

Example 29

Preparation of 4-(benzyloxy)-3-bromo-1-(2-thien-3-ylethyl)pyridin-2(1H)-one

To the material of Example 11 (500 mg, 0.0018 mol) in DMF (5 mL) was added dropwise sodium bis(trimethylsilyl)amide (1M in THF, 2 mL). Contents were stirred one hour before adding dropwise a solution of methanesulfonic acid 2-thiophen-3-yl-ethyl ester (J.A.C.S, 109(6), 1987, 1858-1859) (412 mg, 0.002 mol) in DMF (5 mL). Contents were heated at 75° C. overnight. Contents were allowed to cool, poured into water (100 mL), and extracted into EtOAc, dried over MgSO₄, filtered, and concentrated in vacuo leaving a light yellow oil. The oil was purified by silica gel chromatography eluting with 50% EtOAc/hexanes to give the desired as a white solid, 199 mg (28% yield). mp 134.0-134.3° C. FABHRMS m/z 390.0144 (M+H, C₁₈H₁₇BrNO₂S requires 390.0163). ¹H NMR (CDCl₃/300 MHz): 7.43-7.20 (m, 6H); 6.92-6.80 (m, 3H); 5.90 (d, 1H); 5.20 (s, 2H); 4.13 (t, 2H); 3.10 (t, 2H). Anal. Calcd for C₁₈H₁₆BrNO₂S: C, 55.39; H, 4.13; N, 3.59. Found: C, 55.21; H, 3.87; N, 3.52.

Example 30

Preparation of 4-(benzyloxy)-3-bromo-1-(2-thien-2-ylethyl)pyridin-2(1H)-one

The title compound was prepared essentially according to the procedure of Example 29. mp 128.0-129.5° C. FABHRMS m/z 390.0160 (M+H, C₁₈H₁₇BrNO₂S requires 390.0163). ¹H NMR (CDCl₃/300 MHz) δ: 7.48-7.30 (m, 5H); 7.12 (d, 1H); 6.95-6.80 (m, 2H); 6.75-6.68 (m 1H); 5.95 (d, 1H); 5.20 (s, 2H); 4.16 (t, 2H); 3.30 (t, 2H). Anal. Calcd for C₁₈H₁₆BrNO₂S: C, 55.39; H, 4.13; N, 3.59. Found: C, 55.06; H, 4.01; N, 3.56.

Example 31

Preparation of 4-(benzyloxy)-3-bromo-1-[3-(trifluoromethyl) benzyl]pyridin-2(1H)-one

To the material of Example 11 (500 mg, 0.0018 mol) in DMF (5 mL) was added dropwise sodium bis(trimethylsilyl)amide (1M in THF, 2 mL). Contents were stirred one hour before adding dropwise a solution of 3-trifluoromethylbenzyl bromide (478 mg, 0.002 mol) in DMF (5 mL). Contents were heated at 75° C. for 2 hours. Contents were allowed to cool, poured into water (100 mL), and extracted with EtOAc, which was dried over MgSO₄, filtered, and concentrated in vacuo leaving a white solid. FABHRMS m/z 438.0301 (M+H, C₂₀H₁₆BrF₃NO₂ requires 438.0316). ¹H NMR (CDCl₃/300 MHz): 7.60-7.20 (m, 10H); 6.10 (d, 1H); 5.14 (s, 2H); 5.20 (s, 2H). Anal. Calcd for C₂₀H₁₅BrF₃NO₂: C, 54.81; H, 3.45; N, 3.20. Found: C, 54.81; H, 3.36; N, 3.13.

Example 32

Preparation of 4-(benzyloxy)-3-bromo-1-[2-(trifluoromethyl) benzyl]pyridin-2(1H)-one

The material of Example 32 was prepared according to the procedure of Example 31. FABHRMS m/z 438.0280 (M+H, C₂₀H₁₆BrF₃NO₂ requires 438.0316). ¹H NMR (CDCl₃/300 MHz) δ: 7.68 (d, 1H); 7.55-7.20 (m, 8H); 7.15 (d, 11H); 6.10 (d, 11H); 5.40 (s, 2H); 5.13 (s, 2H). Anal. Calcd for C₂₀H₁₅BrF₃NO₂: C, 54.81; H, 3.45; N, 3.20. Found: C, 54.48; H, 3.36; N, 3.17.

Example 33

Preparation of 4-(benzyloxy)-1-[4-(trifluoromethoxy)benzyl]pyridin-2(1H)-one

The material of Example 33 was prepared according to the procedure of Example 1. FABHRMS m/z 376.1158 (M+H, C₂₀H₁₇F₃NO₃ requires 376.1161). ¹H NMR (CDCl₃/300 MHz) δ: 7.40-7.05 (m, 10H); 6.05-5.95 (m, 2H); 5.06 (s, 2H); 4.98 (s, 2H). Anal. Calcd for C₂₀H₁₆F₃NO₃: C, 64.00; H, 4.30; N, 3.73. Found: C, 63.97; H, 4.26; N, 3.57.

Example 34

Preparation of 4-(benzyloxy)-3-bromo-1-[4-(trifluoromethoxy) benzyl]pyridin-2(1H)-one

The material of Example 34 was prepared according to the procedure of Example 2. FABHRMS m/z 454.0240 (M+H, C₂₀H₁₆BrF₃NO₃ requires 454.0266). ¹H NMR (CDCl₃/300 MHz) δ: 7.45-7.10 (m, 10H); 6.08 (d, 1H); 5.20 (s, 2H); 5.12 (s, 2H). Anal. Calcd for C₂₀H₁₅BrF₃NO₃: C, 52.88; H, 3.33; N, 3.08. Found: C, 52.53; H, 3.09; N, 2.92.

Example 35

Preparation of 1-benzyl-4-(benzyloxy)-6-methylpyridin-2(1H)-one

Step 1: Preparation of 1-benzyl-4-hydroxy-6-methylpyridin-2(1H)-one. 4-hydroxy-6-methyl-2-pyrone (0.2 mol, 25.2 g) and benzylamine (0.2 mol, 21.4 g) were added to water (800 mL) and heated to reflux with stirring for 2 hours. After cooling to room temperature, a light brown solid was collected by filtration. (33.4 g, 77%): ¹H NMR (DMSO-d₆/300 MHz) δ: 10.5 (s, 1H), 7.4-7.1 (m, 5H), 5.8-5.6 (m, 2H), 5.2 (s, 2H), 5.1 (s, 2H), 2.2 (s, 3H). ESHRMS m/z 216.100 (M+H, C₁₂H₁₃NO₂ requires 216.102).

Step 2: Preparation of 1-benzyl-4-(benzyloxy)-6-methylpyridin-2(1H)-one. 1-benzyl-4-hydroxy-6-methylpyridin-2(1H)-one (10 mmol, 2.15 g), dichloromethane (100 mL), benzylbromide (11 mmol, 1.88 g), sodium hydroxide (2.5 N, 20 mmol, 8 mL), and benzyltriethylammonium chloride (0.5 g) were vigorously stirred at room temperature for 16 h. Hydrochloric acid (1 N) was added until the mixture produced an acidic reaction to pH paper. The mixture was then extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated. The product was obtained by flash chromatography eluting with ethyl acetate: hexanes (1:2). The appropriate fractions were concentrated to a clear oil. (1.3 g, 43%): ¹H NMR (DMSO-dr/300 MHz) δ: 7.4-7.1 (m, 10H), 6.0-5.9 (m, 2H), 5.2 (s, 2H), 5.1 (s, 2H), 2.2 (s, 3H). ESHRMS m/z 306.147 (M+H, C₂₀H₁₉NO₂ requires 306.149).

Example 36

Preparation of 1-benzyl-4-(benzyloxy)-3-bromo-6-methylpyridin-2(1H)-one

The product from example 35, 1-benzyl-4-(benzyloxy)-6-methylpyridin-2(1H)-one (4.2 mmol, 1.3 g), acetic acid (50 mL), and sodium acetate (5.0 mmol, 0.41 g) were stirred at room temperature. Bromine (4.2 mmol, 0.67 g) was added drop wise with stirring. After ½ hour, water (100 mL) was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with saturated aqueous sodium bicarbonate solution and brine. After drying over magnesium sulfate and concentrating, the mixture was purified by flash column chromatography eluting with ethyl acetate: hexanes (1:2). The appropriate fractions were concentrated to yield a light oil. (1.0 g, 62%): ¹H NMR (DMSO-d₆/300 MHz) 7.4-7.0 (m, 10H), 6.5 (s, 1H), 5.29 (s, 2H), 5.27 (s, 2H), 2.2 (s, 3H). ESHRMS m/z 384.057 (M+H, C₂₀H₁₈NO₂Br requires 384.060).

Example 37

Preparation of 1-benzyl-4-(benzyloxy)-3,5-dibromo-6-methylpyridin-2(1H)-one

The product from example 35, 1-benzyl-4-(benzyloxy)-6-methylpyridin-2(1H)-one (4.2 mmol, 1.3 g), acetic acid (50 mL), and sodium acetate (5.0 mmol, 0.41 g) were stirred at room temperature. Bromine (4.2 mmol, 0.67 g) was added drop wise with stirring. After ½ hour, water (100 mL) was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organics were washed with saturated aqueous sodium bicarbonate solution and brine. After drying over magnesium sulfate and concentrating, the mixture was purified by flash column chromatography eluting with ethyl acetate: hexanes (1:2). The appropriate fractions were concentrated to yield a white solid. (0.3 g, 15%): ¹H NMR (DMSO-d₆/300 MHz) 7.5-7.0 (m, 10H), 5.42 (s, 2H), 5.07 (s, 2H), 2.45 (s, 3H). ESHRMS m/z 463.966 (M+H, C₂₀H₁₇NO₂Br₂ requires 463.968).

Example 38

Preparation of 1-benzyl-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 1-benzyl-6-methyl-2-oxo-1,2-dihydropyridin-4-yl 4-bromobenzenesulfonate. 1-benzyl-4-hydroxy-6-methylpyridin-2(1H)-one (from example 35) (10 mmol, 2.15 g), N,N′-dimethylformamide (30 mL), potassium carbonate (20 mmol, 2.76 g), and 4-bromobenzenesulfonyl chloride (10 mmol, 2.55 g) were stirred at room temperature for 16 hours. Hydrochloric acid (1N) was added until the mixture was acidic to pH paper. Brine (50 mL) was added and the mixture extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with brine and dried over magnesium sulfate, and filtered. After concentrating, the material was purified by flash column chromatography eluting with ethyl acetate:hexanes (1:2). The appropriate fractions were concentrated to a clear oil, which solidified upon standing several days to a white solid. (3.3 g, 76%): ¹H NMR (DMSO-d₆/400 MHz) 7.9 (m, 4H), 7.32-7.00 (m, 5H), 7.3 (m, 1H), 6.12 (d, J=2.4 Hz, 1H), 6.02 (d, J=2.8 Hz, 1H), 5.20 (s, 2H), 2.2 (s, 3H). ESHRMS m/z 436.002 (M+H, C₁₉H₁₆NO₄SBr requires 436.004).

Step 2: Preparation of 1-benzyl-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one. 1-benzyl-6-methyl-2-oxo-1,2-dihydropyridin-4-yl 4-bromobenzenesulfonate (3.0 mmol, 1.3 g), N,N′-dimethylformamide (30 mL), 3-chlorobenzyl alcohol (3.0 mmol, 0.43 g), and sodium hydroxide (60%, 3.3 mmol, 0.13 g) were stirred at room temperature under nitrogen for 4 hours. Hydrochloric acid (1 N, 10 mL) was added and the mixture extracted with ethyl acetate (3×25 mL). The combined organic extracts were washed with saturated aqueous sodium bicarbonate solution and brine. After drying over magnesium sulfate and concentrating, the mixture was purified by flash column chromatography eluting with ethyl acetate:hexanes (1:1) to obtain a light yellow oil. (14.3 g, 64%): ¹H NMR (DMSO-d₆/300 MHz) δ: 7.4-7.0 (m, 10H), 6.0-5.8 (m, 2H), 5.2 (s, 2H), 5.0 (s, 2H), 2.1 (s, 3H). ESHRMS m/z 340.110 (M+H, C₂₀H₁₈NO₂Cl requires 340.110).

Example 39

Preparation of 1-benzyl-3-bromo-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one

The product of example 38, 1-benzyl-4-[(3-chlorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.91 mmol, 310 Mg), acetic acid (20 mL), and sodium acetate (0.91 mmol, 80 Mg) were stirred at room temperature when bromine (0.91 mmol, 145 Mg) was added. After stirring for one hour, the mixture was concentrated, dissolved in ethyl acetate, and washed successively with saturated aqueous sodium bicarbonate solution, brine, and water. After drying over magnesium sulfate and concentrating, the product was recrystallized from tetrahydrofuran/hexanes to yield a white solid. (240 Mg, 63%): ¹H NMR (DMSO-d₆/300 MHz) 7.6-7.0 (m, 10H), 6.5 (s, 1H), 5.33 (s, 2H), 5.33 (s, 2H), 2.3 (s, 3H). ESHRMS nz/z 420.019 (M+H, C₂₀H₁₇NO₂BrCl requires 420.019).

Example 40

Preparation of 1-benzyl-4-[2,6-(dichlorobenzyl)oxy]pyridin-2(1H)-one

The title compound was prepared essentially as described in claim 1. mp 151.6-152.0° C. ¹H NMR (CDCl₃/300 MHz) δ: 7.31 (m, 8H), 7.12 (d, 1H, J=7.45 Hz), 6.13 (d, 1H, J=2.42 Hz), 5.90 (dd, 1H, J=2.62 Hz), 5.22 (s, 2H), 5.10 (s, 2H). ESHRMS m/z 360.0551 (M+H C₁₉H₁₅Cl₂NO₂ requires 360.0558).

Example 41

Preparation of 1-benzyl-3-bromo-4-[2,6-(dichlorobenzyl)oxy]pyridin-2(1H)-one

1-Benzyl-4-[2,6-(dichlorobenzyl)oxy]pyridin-2(1H)-one (0.400 g, 1.11 mmol) was dissolved in acetic acid (10 mL). Sodium acetate (0.091 g, 1.11 mmol was added, and the mixture was cooled to 15° C. Bromine (0.195 g, 1.22 mmol) was added via syringe. The reaction stirred at room temperature for 2 hours. Water (15 mL) was added, and the mixture transferred to a separatory funnel. Ethyl acetate (50 mL) was added and the layers were separated. The organic phase was washed with aqueous NaHCO₃ (2×25 mL), dried over MgSO₄, filtered, and evaporated to yield a white solid. ¹HNMR (CDCl₃/300 MHz) δ: 7.34 (m, 9H), 6.24 (d, 1H, J=7.65 Hz), 5.37 (s, 2H), 5.18 (s, 2H). ESHRMS m/z 439.9646 (M+H C₁₉H₁₄BrCl₂NO₂ requires 439.9641).

Example 42

Preparation of 1-benzyl-4-[(2-chlorobenzyl)oxy]pyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described in Example 1. mp 124.6-125.0° C. ¹HNMR (CDCl₃/300 MHz) δ: 7.36 (m, 9H), 7.14 (d, 1H, J=7.65 Hz), 6.04 (d, 1H, J=2.62 Hz), 5.98 (d, 1H, J=2.82 Hz), 5.10 (s, 2H), 5.09 (s, 2H). ESHRMS m/z 326.0950 (M+H C₁₉H₁₆ClNO₂ requires 326.0948). Anal. Calc'd. for C₁₉H₁₆ClNO₂: C, 70.05; H, 4.95; N, 4.30; Cl, 10.88. Found: C, 69.87; H, 4.74; N, 4.42, Cl, 11.08.

Example 43

Preparation of 1-benzyl-3-bromo-4-[(2-chlorobenzyl)oxy]pyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described in Example 2. mp 143.3-145.5° C. ¹HNMR (CDCl₃/300 MHz) δ: 7.63 (d, 2H, J=1.81 Hz), 7.44 (m, 9H), 6.06 (d, 1H, J=7.65 Hz), 5.29 (s, 2H), 5.17 (s, 2H). ESHRMS m/z 406.0036 (M+H C₁₉H₁₅BrClNO₂ requires 406.0032). Anal. Calc'd. for C₁₉H₁₅Cl BrNO₂: C, 56.39; H, 3.74; N, 3.46; Cl, 8.76. Found: C, 56.01; H, 3.38; N, 3.36, Cl, 9.01.

Example 44

Preparation of 1-benzyl-3-bromo-4-[(4-methylbenzyl)oxy]pyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described in Example 2. mp 149.0-149.7° C. ¹HNMR (CDCl₃/300 MHz) δ: 7.25 (m, 10H), 6.04 (d, 1H, J=7.65 Hz), 5.17 (s, 2H), 5.15 (s, 2H), 2.34 (s, 3H). ESHRMS m/z 386.0583 (M+H C₂₀H₁₈BrNO₂ requires 386.0581).

Example 45

Preparation of 1-benzyl-4-[(3-chlorobenzyl)oxy]pyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described in Example 1. mp 95.5-95.7° C. ¹HNMR (CDCl₃/300 MHz) δ: 7.34 (m, 9H), 7.13 (d, 1H, J=7.45 Hz), 5.96 (m, 1H), 5.95 (d, 1H, J=7.45 Hz), 5.09 (s, 2H), 4.96 (s, 2H). ESHRMS m/z 326.0977 (M+H C₁₉H₁₆ClNO₂ requires 326.0948).

Example 46

Preparation of 1-benzyl-4-[benzylthio]-3-bromopyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described in Example 2. mp 180.6-182.1° C. ¹HNMR (CDCl₃/300 MHz) δ: 7.33 (m, 10H), 7.14 (d, 1H, J=7.45 Hz), 6.08 (d, 1H, J=7.45 Hz), 5.13 (s, 2H), 4.15 (s, 2H). ESHRMS m/z 386.0211 (M+H C₁₉H₁₆BrNOS requires 386.0214).

Example 47

Preparation of 1-benzyl-3-bromo-4-{[2-(trifluoromethyl)benzyl]oxy}pyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described in Example 2. mp 133.2-133.5° C. ¹HNMR (CDCl₃/300 MHz) δ: 7.81 (d, 1H, J=7.65 Hz), 7.68 (d, 1H, J=7.65 Hz), 7.61 (t, 1H, J=7.65 Hz), 7.38 (m, 7H), 6.01 (d, 1H, J=7.85 Hz), 5.39 (s, 2H), 5.16 (s, 2H). ESHRMS m/z 438.0313 (M+H C₂₀H₁₅BrF₃NO₂ requires 403.0316).

Example 48

Preparation of 1-benzyl-4-(benzyloxy)-3-iodopyridin-2(1H)-one

A mixture of N,O-dibenzyl-2-pyridone (2.0 g, 6.87 mmol), N-iodosuccinimide (1.7 g), dichloroacetic acid (0.15 mL) in acetonitrile (40.0 mL) was heated at 65° C. under argon atmosphere for 3.5 h, with constant stirring. The reaction mixture was concentrated to dryness, and the residue was purified by silica gel flash chromatography using EtOAc/hexanes 1:1 v/v to give the title compound 2.3 g (80%) as a flaky white solid: ¹H-NMR (CDCl₃) δ: 7.4-7.2 (m, 10H), 7.19 (1H, d, J=7.6 Hz), 5.95 (d, 1H, J=7.6 Hz), 5.2 (s, 1H), 5.15 (s, 2H); ER-MS m/z=418 (MH⁺); HR-MS m/z calcd C₁₉H₁₇NO₂ 418.0304, found 418.0277.

Example 49

Preparation of 1-benzyl-4-(benzyloxy)-3-vinylpyridin-2(1H)-one

A solution of 1-benzyl-4-(benzyloxy)-3-iodopyridin-2(1H)-one (1.9 g, 4.56 mmol) and vinyl-tri-butyltin (2.5 mL) in acetonitrile (20 0 mL) containing DMF (2.0 mL) was degassed using house vacuum and purged with argon. Then added PdCl₂(PPh₃)₂ (0.3 g) and the mixture was heated at 65° C. under argon atmosphere for 4 h, with stirring. The solvents were distilled in vacuo, and the residue was triturated with EtOAc and filtered through a pad of celite. The filtrate was concentrated and the residue was purified by silica gel flash chromatography using 25% EtOAc in hexanes to give the title compound (0.75 g. 50%) as an orange colored solid. ¹H-NMR (CDCl₃) δ: 7.4-7.2 (m, 10H), 7.14 (d, 1H, J=7.6 Hz), 7.05 (dd, 1H, J=12.0 Hz), 6.47 (dd, 1H, J=2.8 Hz), 6.07 (d, 1H, J=7.6 Hz), 5.4 (dd, 1H, J=2.8 Hz), 5.13 (s, 4H); ER-MS m/z=418 (MH⁺); ER-MS m/z=318 (MH⁺); HR-MS m/z calcd C₂₁H₂₀NO₂ 318.1494, found 318.1480.

Example 50

Preparation of 1-benzyl-4-(benzyloxy)-3-ethylpyridin-2(1H)-one

To a solution of 1-benzyl-4-(benzyloxy)-3-vinylpyridin-2(1H)-one (0.5 g, 1.6 mmol) in EtOH (10.0 mL) and EtOAc (10.0 mL) was added Pd/C (10%, 0.25 g) and stirred in an atmosphere of hydrogen gas at 30 psi for 16 h. The catalyst was removed by filtration, the filtrate was concentrated to dryness and the resulting residue was purified by silica gel flash chromatography using EtOAc/hexanes (1:1, v/v) to afford the title compound (0.32 g, 64%) as a pale yellow powder: ¹H-NMR (CD₃OD) δ: 7.52 (d, 1H, J=7.6 Hz), 7.39-7.2 (m, 10H), 6.41 (d, 1 h, J=7.6 Hz), 5.18 (s, 2H), 5.15 (s, 2H), 2.58 (q, 2H, J=7.2 Hz), 1.03 (t, 3H, J=7.2 Hz), ER-MS m/z=320 (MH⁺); HR-MS m/z calcd C₂₁H₂₂NO₂ 320.1651, found 320.1648.

Example 51

Preparation of 3-acetyl-4-(benzyloxy)-1-(2-chlorophenyl)-6-methylpyridin-2(1H)-one

Step A. Preparation of 3-acetyl-1-(2-chlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 2-chlorophenylisocyanate (3.0 g, 19.53 mmol), and diketene (3.3 g, 39.28 mmol) in toluene (10.0 mL) containing triethylamine (0.05 mL) was heated to reflux for 6 h, under an atmosphere of argon. Toluene was distilled in vacuo and the resulting residue was purified by silica gel flash chromatography using 25% EtOAc in hexanes as the eluent to afford the title compound (0.85 g, see Heterocycles 27 (9), 2063 (1988)) as a pale yellow solid: ¹H-NMR (CD₃OD) δ: 7.63 (m, 1H), 7.52 (m, 2H), 7.4 (m, 1H), 6.14 (s, 1H), 2.58 (s, 3H), and 1.95 (s, 3H); ES-MS m/z=278 (MH⁺).

Step B. Preparation of 3-acetyl-4-(benzyloxy)-1-(2-chlorophenyl)-6-methylpyridin-2(1H)-one. To a solution of 3-acetyl-1-(2-chlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.56 g, 2.02 mmol) in DMF (5.0 mL), benzyl bromide (0.3 mL) and potassium carbonate (0.3 g, 2.16 mmol) were added. The mixture was stirred at room temperature for 3 h, and at 65° C. for 1 h under argon atmosphere. The reaction mixture was concentrated in vacuo and the residue was partitioned between 5% citric acid (25 mL) and EtOAc (50.0 mL). The organic phase was washed with brine, dried (Na₂SO₄), filtered, and concentrated to dryness. The resulting residue was purified by silica gel flash chromatography using 50% EtOAc in hexanes to afford the title compound (0.58 g, 75%) as a pale yellow amorphous substance: ¹H-NMR (CD₃OD) δ: 7.65-7.3 (m, 9H), 6.5 (s, 1H), 5.31 (s, 2H), 2.42 (s, 3H), and 2.01 (s, 3H); ER-MS m/z=368 (MH⁺); HR-MS m/z calcd C₂₁H₁₉NO₃Cl, 368.1060, found 368.1053.

Example 52

Preparation of 1-benzyl-3-bromo-4-(2-phenylethyl)pyridin-2(1H)-one

Step A. Preparation of 1-benzyl-3-bromo-4-hydroxypyridin-2(1H)-one A suspension of N-benzyl-4-hydroxy-2-pyridone ((0.75 g, 3.7 mmol), NBS (0.7 g, 1.05 mmol) in dichloromethane was stirred at room temperature for 1.5 h under argon atmosphere. It was diluted with dichloromethane (25 mL), cooled and filtered. The solids were washed with dichloromethane and dried in vacuo. The filtrate and the washings were combined and washed with water, dried (Na₂SO₄), filtered, and concentrated to dryness. The resulting residue was washed with EtOAc, and dried in vacuo to give a combined mass of 0.65 g of the title compound as a white powder: 1H NMR (CD₃OD) δ: 7.54 (d, 1H, J=7.6 Hz), 7.27 (m, 5H), 6.12 (d, 1H, J=7.6 Hz), 5.15 (s, 2H); ES-MS: m/z=280 (MH⁺).

Step B. Preparation of 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate To a cold (−30° C.) suspension of 1-benzyl-3-bromo-4-hydroxypyridin-2(1H)-one (0.78 g, 2.8 mmol) in dichloromethane (10.0 mL), was added triethylamine (0.6 mL, 4.28 mmol), followed by the addition of triflic anhydride (0.7 mL, 4.17 mmol). The resulting mixture was stirred at −30° C. under argon atmosphere for 1 h. The reaction mixture was then poured into ice/water mixture (50 mL) and the products were extracted with dichloromethane (2×25 mL). The combined organic extracts were washed with water (2×20 mL), dried (Na₂SO₄), filtered, and concentrated to dryness. The residue was dried in vacuo to afford the desired trifluorosulfonate (1.0 g) as a pale yellow solid which used as such in the next step: ¹H-NMR (CDCl₃) δ: 7.35 (m, 6H), 6.26 (d, 1H, J=8.0 Hz); ¹⁹F-NMR (CDCl₃) δ: −73.73 ppm; ES-MS: m/z=412 (MH⁺).

Step C. Preparation of 1-benzyl-3-bromo-4-(phenylethynyl)pyridin-2(1H)-one. To a solution of 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate (1.0 g) in DMF (5.0 mL) was added phenylacetylene (0.4 mL) and degassed using house vacuum. The reaction flask was then purged with argon, added diisopropylethylamine (0.53 mL), and PdCl₂(PPh₃)₂ (0.35 g) were added. The resulting mixture was stirred at room temperature for 15 min and heated at 65° C. under an argon atmosphere for 3 h. The dark colored reaction mixture was concentrated in vacuo, and the residue was partitioned between EtOAc (50 mL) and 5% aqueous citric acid (25 mL). The organic extracts were washed with water, dried (Na₂SO₄), filtered, and concentrated to dryness. The resulting material was purified by silica gel flash chromatography using 25% EtOAc in hexanes as the eluent. The appropriate fractions were combined, concentrated under reduced pressure. ¹H NMR (CDCl₃) δ: 7.57 (m, 2H), 7.38 (m, 8H), 7.21 (d, 1H, J=6.8 Hz), 6.25 (d, 1H, J=6.8 Hz), and 5.16 (d, 2H), ES-MS: m/z=364 (MH⁺); HR-MS m/z (MH⁺) calcd C₂₀H₁₅NOBr 364.0337, found 364.0337.

Step D. Preparation of 1-benzyl-3-bromo-4-(2-phenylethyl)pyridin-2(1H)-one. A mixture of 1-benzyl-3-bromo-4-(phenylethynyl)pyridin-2(1H)-one (0.3 g), and platinum oxide (0.05 g) in a solvent mixture of EtOAc (10.0 mL) and EtOH (10.0 mL) was stirred in an atmosphere of hydrogen at 15 psi in a Fischer porter bottle for 45 min. The catalyst was removed by filtration, and filtrate was concentrated. The resulting residue was purified by silica gel flash chromatography using 25% EtOAc in hexanes as the eluent. The appropriate fractions (visualized under an UV lamp) were combined and concentrated under reduced pressure. ¹H-NMR (CD₃OD) δ: 7.56 (d, 1H, J=6.8 Hz), 7.31-7.17 (m, 10H), 6.24 (d, 1H, J=6.8 Hz), 5.19 (s, 2H), 2.96 (m, 2H), and 2.91 (m, 2H); ES-MS m/z=368 (MH⁺); HR-MS m/z (MH⁺) calcd C₂₀H₁₉NOBr 368.0650, found 368.0630.

Example 53

Preparation of 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(2-phenylethyl)pyridin-2(1H)-one

The title compound was prepared essentially according to the procedure of Example 52. ¹H-NMR δ: (CD₃OD) δ: 7.35 (m, 1H), 7.31-7.16 (m, 5H), 6.99(m, 1H), 6.91 (m, 1H), 6.81 (m, 1H), 6.20 (s, 1H), 5.41 (s, 2H), 2.94 (m, 4H), and 2.24 (s, 3H); ¹⁹F-NMR (CD₃OD) δ: −115.01 (m); ES-MS, m/z=400 (MH⁺); HR-MS m/z calcd C₂₁H₂₀NOBrF 400.0712, found 400.0695.

Example 54

Preparation of 4-(benzyloxy)-3-bromo-1-(2,6-dichlorophenyl)-6-methylpyridin-2(1H)-one

Step A. Preparation of 3-acetyl-1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 2,6 dichlorophenylisocyanate (4.8 g, 0.025 mol), and diketene (4.3 g, 0.05 mol) in toluene (15.0 mL) was heated to reflux for 4 h under an atmosphere of argon. After removal of the solvent in vacuo, the residue was purified by silica gel flash chromatography using EtOAc/hexanes (1:3 v/v). The appropriate fractions, as monitored by ES mass spectrometry (MH⁺m/z=312) were combined and concentrated under reduced pressure. The resulting yellow solid (2.3 g) was further purified by reverse-phase HPLC using 10-90% acetonitrile/water gradient (45 min) at a flow rate of 100 mL/min. The appropriate fractions, as monitored by ES mass spectrometry (MH⁺m/z=312) were combined and concentrated to half the volume. The solid that separated was extracted with EtOAc (2×25 mL). The combined extracts were washed with water, dried (Na₂SO₄), filtered, and concentrated to dryness to give the title compound (0.77 g) as a pale yellow powder: ¹H-NMR (CD₃OD) δ: 7.62 (m, 2H), 7.52 (m, 1H), 6.19 (s, 1H), 2.59 (s, 3H), and 1.96 (s, 3H); ES-MS m/z=312 (MH⁺); HR-MS, m/z calc C₁₄H₁₂NO₃Cl₂ 312.0189, found 312.0214.

Step B. Preparation of 1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 3-acetyl-1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one 0.7 g (0.002 mol) in n-butanol (3.0 mL) containing sulfuric acid (1.5 mL) was heated at 120° C. for 4 h. The dark reaction mixture was cooled, added ice/water (25 mL), and extracted with EtOAc (2×25 ml). The combined organic extracts were washed with water, dried (Na₂SO₄), filtered, concentrated under reduced pressure and the resulting material was purified by silica gel flash chromatography using 25% EtOAc in hexanes as the eluent to afford the title compound (0.14 g) as a pale yellow powder: ¹H-NMR (CD₃OD) δ: 7.6 (m, 2H), 7.48 (m, 1H), 6.10 (dd, 1H), 5.78 (d, 1H, J=2.4 Hz), 1.91 (s, 3H); ES-MS m/z=270 (MH⁺); HR-MS, m/z calc C₁₂H₁₀NO₂Cl₂ 270.0083, found 270.0103.

Step C. Preparation of 4-(benzyloxy)-1-(2,6-dichlorophenyl)-6-methylpyridin-2(1H)-one A mixture of 1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.125 g, 0.46 mmol) and benzylbromide (0.1 mL) in DMF (2.5 mL) was stirred at room temperature for 16 h. The reaction mixture was diluted with water (10.0 mL) and extracted with EtOAc (2×20 mL). The combined organic extracts were washed with water, dried (Na₂SO₄), filtered, concentrated under reduced pressure and the resulting material was purified by silica gel flash chromatography using 25% EtOAc in hexanes to afford the title compound (0.11 g) as a pale yellow syrup: ¹H-NMR (CD₃OD) δ: 7.61 (m, 2H), 7.55-7.3 (m, 6H), 6.23 (d, 1H, J=2.0 Hz), 6.01 (d, 1H, J=2.0 Hz), 5.12 (s, 2H), and 1.93 (s, 3H); ES-MS m/z=360 (MH⁺); HR-MS, m/z calc C₁₉H₁₆NO₂Cl₂, 360.0553, found 360.0569.

Step D. Preparation of 4-(benzyloxy)-3-bromo-1-(2,6-dichlorophenyl)-6-methylpyridin-2(1H)-one. A mixture of 4-(benzyloxy)-1-(2,6-dichlorophenyl)-6-methylpyridin-2(1H)-one (0.1 g, 0.278 mmol) and N-bromosuccinimide (0.055 g, 0.3 mmol) in dichloroethane (3.0 mL) was stirred at room temperature for 1 h, and heated at 60° C. under argon for 30 min. The reaction mixture was then diluted with dichloroethane (15 mL), washed with water, dried (Na₂SO₄), filtered, and concentrated under reduced pressure. ¹H NMR (CD₃OD) δ: 7.64 (m, 2H), 7.55 (m, 3H), 7.38 (m, 3H), 6.65 (s, 1H), 5.34 (s, 2H), and 2.00 (s, 3H); ES-MS m/z=439 (MH⁺); HR-MS, m/z calc C₁₉H₁₆NO₂Cl₂Br, 439.9635, found 439.9669.

Example 55

Preparation of 3-bromo-1-(3-fluorobenzyl)-4-(2-phenylethyl)pyridin-2(1H)-one

The title compound was prepared essentially according to the procedure of Example 52. ¹H-NMR (CD₃OD) δ: 7.58 (d, 1H, J=6.8 Hz), 7.4-7.0 (m, 9H), 6.26 (d, 1H. J=6.8 Hz), 5.19 (s, 2H), 2.97 (m, 2H), and 2.90 (m, 2H); ES-MS m/z=386 (MH⁺); HR-MS, m/z calc C₂₀H₁₈NOFBr, 386.0550, found 386.0585.

Example 56

Preparation of 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl Methyl(phenyl)carbamate

Step A. Preparation of 1-benzyl-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate To a chilled solution of 1-benzyl-4-hydroxypyridin-2(1H)-one (0.375 g, 1.86 mmol) in anhydrous acetonitrile (10 mL) was added triethylamine (0.206 g, 2.04 mmol) followed by N-methyl-N-phenylcarbamoyl chloride (0.379 g, 2.24 mmol). The reaction mixture was stirred under nitrogen atmosphere at 0° C. for 30 min then at room temperature for 1 h. The reaction was monitored by TLC (5% methanol in dichloromethane). The solvent was removed under reduced pressure and the residue was washed with 10% citric acid and extracted with EtOAc. The organic extracts were combined, washed with water dried over anhydrous Na₂SO₄, and filtered. The solvent was removed under reduced pressure to afford a yellow syrup. The residue was purified by flash chromatography (silica gel) using 5% MeOH in CH₂Cl₂ to give the desired product (0.382 g, 61%) as a white semisolid. MS and ¹H-NMR were consistent with the desired structure. ¹H-NMR (d₆-DMSO, 400 MHz) δ: 7.8 (d, 1H), 7.39 (m, 10H), 6.19 (s, 2H), 5.03 (s, 2H), 3.29 (s, 3H); HR-MS (ES) m/z calcd for C₂₀H₁₈N₂O₃ (MH⁺)=335.1396, observed 335.1418.

Step B. Preparation of 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate To a solution of 1-benzyl-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate (0.38 g, 1.13 mmol) in anhydrous CH₂Cl₂ (7 mL) was added N-Bromosuccinimide (NBS, 0.24 g, 1.34 mmol). The reaction was stirred overnight at room temperature under nitrogen atmosphere. The reaction mixture was purified by flash chromatography (silica gel) using EtOAc/hexanes (1:1 v/v). The appropriate fractions were collected according to ES MS (M+H 413) and concentrated. The dried product showed about 14% of di-brominated product by analytical HPLC. The compounds were separated by reverse phase HPLC using a 10-90% acetonitrile in water, 30 min gradient at a 100 mL/min flow rate, to afford (after lyophilization) the salt of the desired compound. The salt was diluted in EtOAc and washed with NaHCO₃. The organic extracts were dried over anhydrous Na₂SO₄, filtered, and concentrated to afford the desired compound (0.271 g, 58%) as a beige solid. MS and ¹H-NMR were consistent with the desired structure. ¹H-NMR (d₆-DMSO, 400 Hz) δ: 7.83 (d, 1H), 7.39 (m, 10H), 6.48 (s, 1H), 5.12 (s, 2H), 3.33 (s, 3H); HR-MS (ES) m/z calcd for C₂₀H₁₇O₃Br (MH⁺)=413.0495, observed 413.0496.

Example 57

Preparation of 4-(benzyloxy)-3-ethynyl-1-(3-fluorobenzyl)pyridin-2(1H)-one

Step A. Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one Heated a reaction mixture of 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one (4.83 g, 15.6 mmol) in anhydrous acetonitrile (55 mL) and N-iodosuccinimide (NIS, 3.86 g, 17.1 mmol) under nitrogen atmosphere at 65° C. for 4 h. The reaction mixture was concentrated under reduced pressure and the residue was purified by flash chromatography (silica gel) using EtOAc/hexanes (1:1 v:v). The appropriate fractions were collected according to ES MS (M+H 436) and washed with Na₂SO₃ to remove the color impurities. The fractions were concentrated under reduced pressure and dried in vacuo to afford the desired product (6.15 g, 90%) as a light yellow solid. MS and ¹H-NMR were consistent with the desired structure. ¹H-NMR (CD₃OD, 400 Hz) δ: 7.73 (d, 1H), 7.47 (d, 2H), 7.39 (m, 4H), 7.08 (m, 3H), 6.39 (d, 1H), 5.29 (s, 2H), 5.19 (s, 2H); HR-MS (ES) m/z calcd for C₁₉H₁₅NO₂FI (MH⁺)=436.0210, observed 436.0196.

Step B. Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-[(trimethylsilyl)ethynyl]pyridin-2(1H)-one Degassed a solution of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one (2.01 g, 4.62 mmol) in anhydrous acetonitrile (25 mL) under argon atmosphere. Triethylamine (1.11 g, 11 mmol) was added and quickly degassed. The reaction mixture was chilled in an ice bath for 15 minutes before adding bistriphenylphosphine-palladium chloride (0.34 g, 0.48 mmol) and cuprous iodide (0.2 g). The reaction was stirred at room temperature for 30 min before heating at 60° C. under an atmosphere of argon for 2 h. The reaction mixture was filtered through a bed of celite and the filtrate was concentrated under reduced pressure. The dark brown residue was diluted with CH₂Cl₂ (100 mL) and washed with water. The organic extracts were combined, dried over anhydrous Na₂SO₄, filtered, and concentrated under reduced pressure. The dark brown residue was purified by flash chromatography (silica gel) using 30% EtOAc in hexane. The appropriate fractions were combined and concentrated under reduced pressure to afford the desired product (1.34 g, 72%) as a light yellow solid. MS and ¹H-NMR were consistent with the desired structure. ¹H-NMR (CD₃OD, 400 Hz) δ: 7.74 (d, 1H), 7.47 (d, 2H), 7.35 (m, 4H), 7.09 (m, 3H), 6.46 (d, 1H), 5.26 (s, 2H), 5.13 (s, 2H), 0.18 (s, 9H); HR-MS (ES) m/z calcd for C₂₄H₂₄NO₂FSi (MH⁺)=406.1638, observed 406.1610.

Step C. Preparation of 4-(benzyloxy)-3-ethynyl-1-(3-fluorobenzyl)pyridin-2(1H)-one To a solution of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-[(trimethylsilyl)ethynyl]pyridin-2(1H)-one (1.31 g, 3.2 mmol) in anhydrous acetonitrile (25 mL) at 0° C. was added tetrabutylammonium fluoride (0.611 g, 1.93 mmol). The reaction was stirred at 0° C. for 15 min then for 1 h at room temperature. The reaction was concentrated under reduced pressure and the residue was diluted with EtOAc and washed with water. The organic extracts were combined, dried over anhydrous Na₂SO₄, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel) using EtOAc in hexanes (1:1 v/v). The appropriate fractions were combined and concentrated under reduced pressure to afford the desired product (0.779 g, 72%) as a gold solid. MS and ¹H-NMR were consistent with the desired structure. ¹H-NMR (CD₃OD, 400 Hz) δ: 7.73 (d, 1H), 7.43 (d, 2H), 7.35 (m, 4H), 7.09 (m, 3H), 6.45 (d, 1H), 5.27 (s, 2H), 5.13 (s, 2H), 3.78 (s, 1H); HR-MS (ES) m/z calcd for C₂₁H₁₆NO₂F (MH⁺)=334.1243, observed 334.1234.

Example 58

Preparation of 4-(benzylamino)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one

Step A. Preparation of 1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one In a Fischer-Porter bottle, added a solution of 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one (4.5 g, 14.56 mmol) in absolute ethanol (20 mL). Flushed the solution with nitrogen then added palladium catalyst (1.05 g). Sealed bottle and evacuated system. The system was purged with hydrogen gas (2×15 psi) to check for leaks. The reaction was charged with hydrogen (35 psi) and stirred at room temperature for 45 min. The system was evacuated and flushed with nitrogen. The reaction was filtered and the catalyst was carefully washed with fresh ethanol. The filtrate was concentrated under reduced pressure. MS and ¹H-NMR were consistent with the desired structure. ¹H-NMR (CD₃OD, 400 Hz) δ: 7.54 (d, 1H), 7.32 (m, 1H), 7.06 (m, 3H), 6.05 (dd, 1H), 5.83 (s, 1H), 5.09 (s, 2H); HR-MS (ES) m/z calcd for C₁₂H₁₀NO₂F (MH⁺)=220.0774, observed 220.0787.

Step B. Preparation of 4-(benzylamino)-1-(3-fluorobenzyl)pyridin-2(1H)-one Heated a reaction mixture of 1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one (1.005 g, 4.5 mmol) in benzylamine (15 mL) at reflux (185° C.) under nitrogen atmosphere for 24 h. The reaction was monitored by ES-MS (MH+ 309). The solvent was removed by vacuum distillation to give a yellow residue. MS and ¹H-NMR were consistent with the desired structure. ¹H-NMR (CD₃OD, 400 Hz) δ: 7.31 (m, 7H), 7.03 (m, 3H), 5.98 (dd, 1H), 5.45 (s, 1H), 5.00 (s, 2H), 4.30 (s, 2H); HR-MS (ES) m/z calcd for C₁₉H₁₇N₂OF (MH⁺)=309.1403, observed 309.1375.

Step C. Preparation of 4-(benzylamino)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one To a solution of 4-(benzylamino)-1-(3-fluorobenzyl)pyridin-2(1H)-one (0.50 g, 1.62 mmol) in anhydrous CH₂Cl₂ (10 mL) was added N-bromosuccinimide (NBS, 0.30 g, 1.7 mmol). The reaction was stirred at room temperature under a nitrogen atmosphere for 3 h. The reaction mixture was purified by flash chromatography (silica gel) using EtOAc in hexanes (1:1 v/v). The appropriate fractions were combined and concentrated. MS and ¹H-NMR were consistent with the desired structure. ¹H-NMR (CD₃OD, 400 Hz) δ: 7.41 (d, 1H), 7.31 (m, 6H), 7.04 (m, 3H), 5.99 (d, 1H), 5.08 (s, 2H), 4.53 (s, 2H); HR-MS (ES) m/z calcd for C₁₉H₁₆N₂OFBr (MH⁺)=387.0508, observed 387.0504.

Example 59

Preparation of 3-bromo-1-cyclopropylmethyl-4-(4-fluorobenzyloxy)-1H-pyridin-2-one

Step 1. Preparation of 4-[(4-fluorobenzyloxy]pyridine-1-oxide. To an ice-cold solution of sodium hydride (1.9 g, of a 60% dispersion in mineral oil, 46 mmol) in DMF (39 mL) was added 4-fluorobenzyl alcohol (5.1 mL, 46 mmol). The reaction mixture was warmed to room temperature, 4-chloropyridine-1-oxide¹ (5.0 g, 39 mmol) was added, and the reaction mixture was stirred for 6 h. The reaction mixture was diluted with a 50% aqueous solution of brine, and extracted with CHCl₃ (7×50 mL). The combined organics were dried (MgSO₄), filtered, and concentrated under reduced pressure. Trituration with Et₂O afforded 4-[(4-fluorobenzyloxy]pyridine-1-oxide as an off-white solid (9.1 g, 90%), which was used in the next step without further purification or characterization.

Step 2. Preparation of 4-(4-fluorobenzyloxy)-1H-pyridin-2-one. A solution of 4-[(4-fluorobenzyloxy]pyridine-1-oxide (6.4 g, 29 mmol) in acetic anhydride (97 mL) was heated at reflux for 3 h. The reaction mixture was cooled to room temperature and the solvent was removed under reduced pressure. The residue was diluted with 1:1 MeOH/water (34 mL), and the mixture was stirred at room temperature for 1 h. The solvent was removed under reduced pressure. Trituration with Et₂O/hexanes afforded 4-(4-fluorobenzyloxy)-1H-pyridin-2-one as a brown solid (3.1 g, 48%): ¹H NMR (300 MHz, CDCl₃) δ 7.40-7.36 (m, 2H), 7.22 (d, J=8 Hz, 1H), 7.09 (t, J=7 Hz, 2H), 6.03 (dd, J=7, 3 Hz, 1H), 5.94 (d, J=3 Hz, 1H), 4.98 (s, 2H).

Step 3. Preparation of 3-bromo-4-(4-fluorobenzyloxy)-1H-pyridin-2-one. To an ice-cold solution of 4-(4-fluorobenzyloxy)pyridine-2(1H)-one (3.1 g, 14 mmol) in AcOH (26 mL) was added a solution of bromine (0.79 mL, 15 mmol) in AcOH (51 mL), and the reaction mixture was stirred at room temperature for 2 h. The solvent was removed under reduced pressure, and purification by flash column chromatography (silica, 1:1 Et₂O/hexanes) to afford 3-bromo-4-(4-fluorobenzyloxy)-1H-pyridin-2-one as an orange solid (0.78 g, 48%): MS APCI m/z 298 [M+H]⁺.

Step 4. Preparation of 3-Bromo-1-cyclopropylmethyl-4-(4-fluorobenzyloxy)-1H-pyridin-2-one. To a solution of 3-bromo-4-(4-fluorobenzyloxy)-1H-pyridin-2-one (0.25 g, 0.84 mmol) in DMF (13 mL) was added K₂CO₃ (0.33 g, 1.7 mmol) and cyclopropylmethyl bromide (0.14 g, 1.0 mmol), and the reaction mixture was stirred at 110° C. for 2 h. The reaction mixture was cooled to room temperature, and the solvent was removed under reduced pressure. The residue was diluted with a 50% aqueous solution of brine, and extracted with CHCl₃ (3×50 mL). The combined organics were washed with water and then brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:1 EtOAc/hexanes) afforded 3-bromo-1-cyclopropyl-methyl-4-(4-fluorobenzyloxy)-1H-pyridin-2-one as a yellow solid (0.12 g, 39%): mp 139-141° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.43-7.34 (m, 3H), 7.07 (t, J=9 Hz, 2H), 6.06 (d, J=6 Hz, 1H), 5.19 (s, 2H), 3.82 (d, J=9 Hz, 2H), 1.26-1.23 (m, 1H), 0.62-0.57 (m, 2H), 0.40-0.36 (m, 2H). ESHRMS m/z 352.0368 (M+H C₁₆H₁₆BrFNO₂ requires 352.0343).

Examples 60-69

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 60-69 are prepared essentially according to the procedures set forth above for Example 59.

Example			M + H	ESHRMS
No.	R	MF	Requires	m/z
Ex. 60	pyridin-4-
	ylmethyl
Ex. 61	pyridin-3-	C18H14BrFN2O2	489.0296	489.0281
	ylmethyl
Ex. 62	4-tert-butyl-	C23H23BrFNO2	444.0969	444.0971
	benzyl
Ex. 63	3-trifluorometh-	C20H14BrF4NO2	456.0217	456.0202
	ylbenzyl
Ex. 64	Biphenyl-2-	C25H19BrFNO2	464.0656	464.0656
	ylmethyl
Ex. 65	4-methoxybenzyl	C20H17BrFNO3	418.0449	418.0457
Ex. 66	4-cyanobenzyl	C20H14BrFN2O2	413.0295	413.0287
Ex. 67	4-trifluoro-	C20H14BrF4NO2	456.0217	456.0192
	methylbenzyl
Ex. 68	Biphenyl-4-	C25H19BrFNO2	464.0656	464.0653
	ylmethyl
Ex. 69	cyclohexylmethyl	C19H21BrFNO2	394.0812	394.0797

NMR characterization of compounds of Examples 12-19

Ex. No. NMR Data
Ex. 60  1H NMR (300MHz, CDCl3) δ 8.57(dd, J=6, 3Hz, 2H), 7.43-7.38(m, 2H), 7.16(d, J=6Hz,
        2H), 7.09(t, J=9Hz, 2H), 6.12(d, J=6Hz, 1H), 5.20(s, 2H), 5.16(s, 2H)
Ex. 61  1H NMR (300MHz, CDCl3) δ 8.58-8.55(m, 2H), 7.75(d, J=6Hz, 1H), 7.41-7.37(m, 2H),
        7.31-7.26(m, 2H), 7.12-7.04(m, 2H), 5.17(d, J=6Hz, 1H), 5.18(s, 2H), 5.16(s, 2H)
Ex. 62  1H NMR (300MHz, MeOD) δ 7.75(d, 1H, J=9Hz), 7.59(t, J=9Hz, 2H), 7.37(d, J=9Hz,
        2H), 7.22(d, J=9Hz, 2H), 7.06-6.99(m, 2H), 6.52(d, J=9Hz, 1H), 5.29(s, 2H), 5.18
        (s, 2H), 1.28(s, 9H)
Ex. 63  1H NMR (300MHz, CDCl3) δ 7.58-7.37(m, 5H), 7.29-7.26(m, 2H), 7.08(t, J=7Hz, 2H),
        6.10(d, J=1Hz, 1H), 5.20(s, 2H), 5.18(s, 2H)
Ex. 64  1H NMR (300 MHz, CDCl3) δ 7.42-7.27(m, 11H), 7.07(t, J=6Hz, 2H), 6.72(d, J=7Hz,
        1H), 5.88(d, J=9Hz, 1H), 5.16(s, 2H), 5.12(s, 2H)
Ex. 65  1H NMR (300MHz, CDCl3) δ 7.38-7.36(m, 2H), 7.27-6.84(m, 3H), 7.08(s, 2H), 6.86(d, J=1Hz
        , 2H), 6.01(d, J=6Hz, 1H), 5.15(s, 2H), 5.09(s, 2H), 3.78(s, 3H)
Ex. 66  1H NMR (300MHz, CDCl3) δ 7.64-7.61(m, 2H), 7.42-7.37(m, 4H), 7.27-7.25(m, 1H),
        7.12-7.06(m, 2H), 6.11(d, J=6Hz, 1H), 5.19(s, 4H)
Ex. 67  1H NMR (300 MHz, CDCl3) δ 7.59(d, J=6Hz, 2H), 7.43-7.37(m, 4H), 7.29-7.25(m, 1H),
        7.08(t, J=6Hz, 2H), 6.08(d, J=9Hz, 1H), 5.20(s, 2H), 5.18(s, 2H)
Ex. 68  1H NMR (300MHz, CDCl3) δ 7.57-7.54(m, 4H), 7.45-7.34(m, 7H), 7.30-
        7.26(m, 1H), 7.08(t, J=9Hz, 2H), 6.06(d, J=6Hz, 1H), 5.20(s, 2H), 5.17
        (s, 2H)
Ex. 69  1H NMR (300MHz, CDCl3) δ 7.93(d, J=6Hz, 1H), 7.45-7.40(m, 2H), 7.29-7.26(m, 1H),
        7.09(t, J=9Hz, 2H), 6.50(d, J=6Hz, 1H), 5.17(s, 2H), 4.14(d, J=6Hz, 2H), 1.90-1.74
        (m, 5H), 1.32-1.05(m, 5H)

Example 70

Preparation of {3-[3-bromo-4-(4-fluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzyl}carbamic Acid Tert-Butyl Ester

Step 1. Preparation of 3-hydroxymethylbenzonitrile. To an ice-cold solution of 3-cyanobenzaldehyde (5.0 g, 38 mmol) in 1:1 MeOH/THF (90 mL) was added NaBH₄ (1.6 g, 42 mmol), and the reaction mixture was stirred for 3 h. The reaction mixture was diluted with brine, and the solvent was removed under reduced pressure. The residue was dissolved in water, and the aqueous layer was extracted with Et₂O (3×100 mL). The combined organics were washed with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure to provide 3-hydroxymethyl-benzonitrile (4.95 g, 98%) as a clear oil, which was used in the next step without further purification or characterization.

Step 2. Preparation of 3-(tert-butyldimethylsilyloxymethyl)benzonitrile. To an ice-cold solution of 3-hydroxymethyl benzonitrile (4.95 g, 37 mmol) in CH₂Cl₂ (47 mL) was added imidazole (5.1 g, 74 mmol), DMAP (0.45 g, 3.7 mmol), and TBSCl (6.2 g, 41 mmol), and the reaction mixture was stirred for 12 h. The reaction mixture was diluted with water, and the aqueous layer was extracted with CH₂Cl₂ (3×150 mL). The combined organics were washed with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure to provide 3-(tert-butyldimethylsilyloxymethyl)-benzonitrile (9.1 g, 99%) as a clear oil: ¹H NMR (300 MHz, CDCl₃) δ 7.51 (s, 1H), 7.42 (d, J=6 Hz, 1H), 7.35-7.28 (m, 1H), 4.75 (s, 2H), 0.94 (s, 9H), 0.11 (s, 6H).

Step 3. Preparation of 3-(tert-butyldimethylsilyloxymethyl)benzylamine. To an ice-cold solution of 3-(tert-butyldimethylsilyloxymethyl)benzonitrile (4.5 g, 18 mmol) in THF (47 mL) was added LiAlH₄ (27 mL, of a 1 M solution in THF, 27 mmol), and the reaction mixture was stirred at reflux for 3 h. The reaction mixture was cooled to 0° C., and the reaction was quenched with water (25 mL) and 15% NaOH in water (75 mL). The reaction mixture was filtered, concentrated under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with water and then brine, dried (MgSO₄), filtered, and concentrated under reduced pressure to provide 3-(tert-Butyldimethylsilyloxymethyl)benzylamine (1.4 g, 30%) as a clear oil: ¹H NMR (300 MHz, CDCl₃) δ 7.22-7.10 (m, 4H), 4.57 (s, 2H), 3.74 (s, 2H), 0.84 (s, 9H), 0.09 (s, 6H).

Step 4. Preparation of 3-(hydroxymethyl)benzylcarbamic acid tert-butyl ester. To a solution of 3-(tert-butyldimethylsilyloxymethyl)benzylamine (1.4 g, 5.5 mmol) and Et₃N (1.5 mL, 11 mmol) in CH₂Cl₂ (28 mL) was added di-tert-butyl dicarbonate (1.3 g, 5.8 mmol), and the reaction mixture was stirred for 12 h. The reaction mixture was diluted with water and extracted with CH₂Cl₂ (3×100 mL). The combined organics were washed with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, CH₂Cl₂) to afford 3-(hydroxymethyl)benzylcarbamic acid tert-butyl ester as a yellow oil (1.4 g, 46%): ¹H NMR (300 MHz, CDCl₃) δ 7.32-7.28 (m, 1H), 7.18 (d, J=8 Hz, 1H), 7.12 (s, 1H), 7.08-7.01 (m, 1H), 4.60 (s, 2H), 4.04 (d, J=6 Hz, 2H), 1.36 (s, 9H).

Step 5. Preparation of 3-(bromomethyl)benzylcarbamic acid tert-butyl ester. To an ice-cold solution of 3-(hydroxymethylbenzyl)carbamic acid tert-butyl ester (0.7 g, 3.0 mmol) and CBr₄ (1.0 g, 3.1 mmol) in THF (14 mL) was added Ph₃P (0.81 g, 3.1 mmol), and the reaction mixture was stirred for 18 h. The reaction mixture was filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent 5:95 to 15:85 EtOAc/hexanes) to afford the 3-(bromomethyl)benzyl-carbamic acid tert-butyl ester as a white solid (0.42 g, 51%): ¹H NMR (300 MHz, MeOD) δ 7.55 (s, 1H), 7.32-7.27 (m, 2H), 7.21-7.19 (m, 1H), 4.54 (s, 2H), 4.21 (s, 2H), 1.28 (s, 9H).

Step 6. Preparation of 1{3-[3-bromo-4-(4-fluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzyl}carbamic acid tert-butyl ester. To a solution of 3-bromo-4-(4-fluorobenzyloxy)pyridine-2(1H)-one (from Step 3, synthesis Example 59) (0.2 g, 0.67 mmol) in DMF (11 mL) was added K₂CO₃ (0.26 g, 1.3 mmol) and 3-(bromomethyl)benzylcarbamic acid tert-butyl ester (0.23 g, 0.80 mmol), and the reaction mixture was stirred at 80° C. for 3 hours. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. The residue was diluted with a 50% aqueous solution of brine (24 mL), and extracted with CHCl₃ (4×50 mL). The combined organics was washed water and then brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 3:7 EtOAc/hexanes) and recrystallization from MeOH afforded {3-[3-bromo-4-(4-fluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzyl}carbamic acid tert-butyl ester as an off-white solid (0.07 g, 20%): mp 136-138° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.42-7.37 (m, 2H), 7.30-7.20 (m, 5H), 7.08 (t, J=9 Hz, 2H), 6.04 (d, J=9 Hz, 1H), 5.16 (s, 2H), 5.14 (s, 2H), 4.28 (d, J=6 Hz, 1H), 1.44 (s, 9H). ESHRMS m/z 517.1124 (M+H C₂₅H₂₇BrFN₂O₄ requires 517.1133).

Example 71

Preparation of 1-(3-aminomethylbenzyl)-3-bromo-4-(4-fluorobenzyloxy)-1H-pyridin-2-one

To an ice-cold solution of 1-[3-{N-tert-butoxycarbonyl}aminomethylbenzyl]-3-bromo-4-(4-fluorobenzyloxy)pyridine-2(1H)-one (Example 69) (0.05 g, 0.1 mmol) in CH₂Cl₂ (2 mL) was added TFA (2 mL), and the reaction mixture was stirred for 1 h. The solvent was removed under reduced pressure to provide 1-(3-aminomethylbenzyl)-3-bromo-4-(4-fluorobenzyloxy)-1H-pyridin-2-one as a tan solid (0.049 g, 100%), as the TFA salt: mp 127-139° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 8.13 (br s, 2H), 7.94 (d, J=6 Hz, 1H), 7.52-7.47 (m, 2H), 7.44-7.37 (m, 2H), 7.27 (t, J=8 Hz, 3H), 6.53 (d, J=8 Hz, 1H), 5.30 (s, 2H), 5.14 (s, 2H), 4.01 (d, J=6 Hz, 2H), 3.39 (br s, 2H); Anal. Calcd for C₂₀H₁₇BrF₂N₂O₂.1.125 TFA: C, 48.99; H, 3.53; N, 5.13. Found: C, 48.80; H, 3.43; N, 4.75. ESHRMS m/z 417.0608 (M+H C₂₀H₁₉BrFN₂O₂ requires 417.0609).

Example 72

Preparation of methyl 2-[3-Bromo-4-(4-fluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzoate

The title compound was prepared by a procedure similar to the one described for EXAMPLE 59 (0.36 g, 48%): mp 161-165° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.98 (d, J=6 Hz, 1H), 7.51-7.26 (m, 6H), 7.11-7.05 (m, 2H), 6.05 (d, J=8 Hz, 1H), 5.60 (s, 2H), 5.18 (s, 2H), 3.93 (s, 3H). ESHRMS m/z 446.0430 (M+H C₂₁H₁₈BrFNO₄ requires 418.0398).

Example 73

Preparation of 3-bromo-4-(4-fluorobenzyloxy)-1-(2-hydroxymethylbenzyl)-1H-pyridin-2-one

To an ice-cold solution of 3-bromo-4-(4-fluorobenzyloxy)-1-(2-hydroxymethylbenzyl)-1H-pyridin-2-one (Example 72) (0.25 g, 0.56 mmol) in THF (1 mL) was added LiBH₄ (2.0 M solution in THF, 0.56 mmol), and the reaction mixture was stirred at 40° C. for 6 hours. The reaction mixture was cooled to room temperature, the solvent was removed under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with brine, dried (MgSO₄), filtered, and concemtrated under reduced pressure. ¹H NMR (300 MHz, DMSO-d₆) δ 7.82 (d, J=8 Hz, 1H), 7.54-7.49 (m, 2H), 7.41 (d, J=7 Hz, 1H), 7.29-7.21 (m, 4H), 6.81 (d, J=7 Hz, 1H), 6.53 (d, J=8 Hz, 1H), 5.30-5.25 (m, 3H), 5.18 (s, 2H), 4.60 (d, J=7 Hz, 2H). ESHRMS m/z 418.0437 (M+H C₂₀H₁₈BrFNO₃ requires 418.0449).

Example 74

Preparation of 3-bromo-4-(2,4-difluorobenzyloxy)-1-[(4-dimethylaminomethyl)benzyl]-1H-pyridin-2-one

Step 1. Preparation of 4-(2,4-difluorobenzyloxy)pyridine-1-oxide. To an ice-cold solution of sodium hydride (1.2 g of a 60% dispersion in mineral oil, 51 mmol) in DMF (43 mL) was added 2,4-difluorobenzyl alcohol (5.7 mL, 51 mmol). The reaction mixture was warmed to room temperature, 4-chloropyridine-1-oxide¹ (5.5 g, 43 mmol) was added, and the reaction mixture was stirred for 6 h. The reaction mixture was diluted with a 50% aqueous solution of brine, and extracted with CHCl₃ (7×50 mL). The combined organics were dried (MgSO₄), filtered, and the solvent was removed under reduced pressure. Trituration with Et₂O afforded 4-(2,4-difluorobenzyloxy)pyridine-1-oxide as an off-white solid (9.1 g, 90%): ¹H NMR (300 MHz, CDCl₃) δ 8.16-8.08 (m, 1H), 7.47-7.36 (m, 1H), 6.97-6.81 (m, 1H), 5.09 (d, J=8 Hz, 1H).

Step 2. Preparation of 4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one. A solution of 4-(2,4-difluorobenzyloxy)pyridine-1-oxide (13.4 g, 57 mmol) in acetic anhydride (30 mL) was stirred at reflux for 4 h. The solvent was removed under reduced pressure, the residue was diluted with 1:1 MeOH/water (60 mL), and the mixture was stirred at room temperature for 1 h. The solvent was removed under reduced pressure. Purification by flash column chromatography (silica, eluent methylene chloride to 9:1 methylene chloride/methanol) provided 4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one as a light brown solid (4.2 g, 31%): ¹H NMR (300 MHz, CDCl₃) δ 7.43 (q, J=8 Hz, 1H), 7.23 (d, J=7 Hz, 1H), 6.91-6.87 (m, 2H), 6.02 (dd, J=8, 2 Hz, 1H), 5.97 (d, J=2 Hz, 1H), 5.03 (s, 2H).

Step 3. Preparation of 3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one. To an ice-cold solution of 4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one (0.75 g, 3.1 mmol) in AcOH (12 mL) was added a solution of bromine (0.2 mL, 3.5 mmol) in AcOH (6 mL), and the reaction mixture was stirred 10 min. The solvent was removed under reduced pressure to afford 3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one as a white solid (1.0 g, 100%): ESI MS m/z 299 [M+H]+.

Step 4. Preparation of 3-bromo-1-(4-chloromethylbenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one. To a solution of 3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one (0.60 g, 2.5 mmol) in DMF (40 mL) was added K₂CO₃ (0.70 g, 5.1 mmol) and □□′-dichloro-p-xylene (0.53 g, 3.0 mmol), and the reaction mixture was stirred at 110° C. for 2 h. The reaction mixture was cooled to room temperature, diluted with brine, and extracted with CHCl₃ (4×100 mL). The combined organics were washed water and then brine, dried (Na₂SO₄), filtered, and concentrated under reduced pressure to afford 3-bromo-1-(4-chloromethylbenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one as an off-white solid (0.49 g, 43%): ¹H NMR (300 MHz, CDCl₃) δ 7.54 (app q, J=8 Hz, 1H), 7.38-7.28 (m, SH), 6.94 (td, J=8, 2 Hz, 1H), 6.85 (td, J=8, 2 Hz, 1H), 6.10 (d, J=9 Hz, 1H), 5.21 (s, 2H), 5.16 (s, 2H), 4.56 (s, 2H).

Step 5. Preparation of 3-bromo-4-(2,4-difluorobenzyloxy)-1-[(4-dimethylaminomethyl)benzyl]-1H-pyridin-2-one. To a sealed tube containing 3-bromo-1-(4-chloromethylbenzyl)-4-(2,4-difluoro-benzyloxy)-1H-pyridin-2-one (0.49 g, 1.1 mmol) was added a solution of dimethylamine (5.5 mL of a 2.0 M solution in THF, 11 mmol), and the reaction mixture was stirred for 15 h. The solvent was removed under reduced pressure. Purification by flash column chromatography (silica, eluent methylene chloride to 92:7.2:0.8 methylene chloride/methanol/ammonia) provided 3-bromo-4-(2,4-difluorobenzyloxy)-1-(4-dimethylaminomethylbenzyl)-1H-pyridin-2-one as a light yellow solid (0.23 g, 46%): mp 111-113° C.; ¹H NMR (500 MHz, CDCl₃) δ 7.50-7.49 (m, 1H), 7.26-7.22 (m, 5H), 6.90-6.88 (m, 1H), 6.82-6.78 (m, 1H), 6.04 (d, J=6 Hz, 1H), 5.16 (s, 2H), 5.11 (s, 2H), 3.37 (s, 2H), 2.19 (s, 6H). ESHRMS m/z 463.0782 (M+H C₂₂H₂₂BrF₂N₂O₂ requires 463.0827).

Example 75

Preparation of 3-bromo-4-(2,4-difluorobenzyloxy)-1-[3-(isopropylaminomethyl)benzyl]-1H-pyridin-2-one

The title compound was prepared by a procedure similar to the one described for Example 74 (0.06 g, 35%): mp 109-110° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.54 (d, J=6 Hz, 1H), 7.33-7.20 (m, 5H), 6.94-6.81 (m, 2H), 6.10 (d, J=6 Hz, 1H), 5.20 (s, 2H), 5.14 (s, 2H), 3.77 (s, 2H), 2.88 (t, J=6 Hz, 1H), 1.13 (d, J=6 Hz, 6H). ESHRMS m/z 477.0955 (M+H C₂₃H₂₄BrF₂N₂O₂ requires 477.0984).

Example 76

Preparation of 3-bromo-4-(2,4-difluorobenzyloxy)-1-[(3-dimethylaminomethyl)benzyl]-1H-pyridin-2-one

The title compound was prepared by a procedure similar to the one described for Example 74 (0.06 g, 25%): mp 103-107° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.52 (d, J=8 Hz, 1H), 7.32-7.24 (m, 5H), 6.94 (td, J=9, 3 Hz, 1H), 6.84 (td, J=9, 3 Hz, 1H), 6.08 (d, J=8 Hz, 1H), 5.20 (s, 2H), 5.16 (s, 2H), 3.44 (s, 2H), 2.24 (s, 6H). ESHRMS m/z 463.0801 (M+H C₂₂H₂₂BrF₂N₂O₂ requires 463.0827).

Example 77

Preparation of 3-Bromo-4-(2,4-difluorobenzyloxy)-1-[(3-methylaminomethyl)benzyl]-1H-pyridin-2-one

The title compound was prepared by a procedure similar to the one described for Example 74 (0.05 g, 16%): mp 107-111° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.55 (d, J=6 Hz, 1H), 7.31-7.19 (m, 5H), 6.94-6.81 (m, 2H), 6.09 (d, J=6 Hz, 1H), 5.20 (s, 2H), 5.14 (s, 2H), 3.73 (s, 2H), 2.45 (s, 1H). ESHRMS m/z 449.0652 (M+H C₂₁H₂₀BrF₂N₂O₂ requires 449.0671).

Example 78

Preparation of {3-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzyl}carbamic Acid Tert-Butyl Ester

The title compound was prepared essentially according to the procedure described in Example 70. mp 80-84° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 7.60-7.50 (m, 1H), 7.33-7.21 (m, 5H), 6.97-6.81 (m, 2H), 6.10 (dd, J=8, 2 Hz, 1H), 5.20 (s, 2H), 5.15 (s, 2H), 4.87 (br s, 2H), 4.30 (s, 2H) 1.45 (s, 9H). ESHRMS m/z 535.1019 (M+H C₂₅H₂₆BrF₂N₂O₄ requires 535.1039).

Example 79

Preparation of 1-[(3-aminomethyl)benzyl]-3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

To an ice-cold solution of {3-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzyl)}carbamic acid tert-butyl ester (Example 78) (0.05 g, 0.1 mmol) in CH₂Cl₂ (2 mL) was added TFA (2 mL), and the reaction mixture was stirred for 1 hour. The solvent was removed under reduced pressure to provide 1-[(3-aminomethyl)benzyl]-3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one as a tan solid (0.049 g, 100%), as the TFA salt: mp 80-84° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 8.15 (br s, 3H), 7.97 (d, J=8 Hz, 1H), 7.79-7.60 (m, 1H), 7.44-7.30 (m, 4H), 7.20-7.15 (m, 1H), 6.61 (d, J=6 Hz, 1H), 5.31 (s, 2H), 5.16 (s, 2H), 4.03 (s, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −74.56 (4.8F), −109.63 (1F), −113.61 (1F). ESHRMS m/z 435.0540 (M+H C₂₀H₁₈BrF₂N₂O₂ requires 435.0515).

Example 80

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-[4-(isopropylaminomethyl)benzyl]-1H-pyridin-2-one

Step 1. Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one. To a solution of 4-[(4-fluorobenzyl)oxy]pyridine-2(1H)-one (from Step 2, Example 74) (1.4 g, 5.9 mmol) in AcOH (25 mL) was added N-chlorosuccinimide (0.95 g, 7.1 mmol) and the reaction mixture was heated at reflux for 2 h. The solvent was removed under reduced pressure. ¹H NMR (300 MHz, MeOD) δ 7.63-7.55 (m, 1H), 7.45(d, J=8 Hz, 1H), 7.07-7.00 (m, 2H), 6.58 (d, J=8 Hz, 1H), 5.31 (d, J=8 Hz, 1H).

Step 2. Preparation of 3-chloro-1-(4-chloromethylbenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one. 3-Chloro-1-(4-chloromethylbenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one was prepared by procedure similar to the one described for 3-bromo-1-(4-chloromethyl-benzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one (Step 3) as white solid (0.24 g, 34%): ¹H NMR (300 MHz, CDCl₃) δ 7.53 (app q, J=9 Hz, 1H), 7.34 (app q, J=9 Hz, 1H), 7.23 (d, J=8 Hz, 1H), 6.94 (td, J=10, 2 Hz, 1H), 6.85 (td, J=10, 2 Hz, 1H), 6.14 (d, J=8 Hz, 1H), 5.20 (s, 2H), 5.16 (s, 2H), 4.56 (s, 2H).

Step 3. Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-[4-(isopropylamino-methyl)benzyl]-1H-pyridin-2-one. The title compound was prepared by a procedure similar to the one described for Example 74 (0.17 g, 69%): mp 146-151° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.52 (app q, J=9 Hz, 1H), 7.35-7.21 (m, 5H), 6.94 (td, J=8, 2 Hz, 1H), 6.85 (td, J=8, 2 Hz, 1H), 6.18 (d, J=8 Hz, 1H), 5.22 (s, 2H), 5.08 (s, 2H), 3.81 (s, 2H), 2.98 (br s, 1H), 1.20 (s, 6H). ESHRMS m/z 433.1481 (M+H C₂₃H₂₄ClF₂N₂O₂ requires 433.1489).

Example 81

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-[(3-methanesulfonyl)benzyl]-1H-pyridin-2-one

Step 1. Preparation of (3-methanesulfonyl)phenyl methanol. To an ice-cold solution of 3-(methylsulfonyl)benzoic acid (1.4 g, 7.1 mmol) in 2:1 Et₂O/THF (60 mL) was added LiAlH₄ (8.5 mL of 1.0 M solution in THF, 8.5 mmol), and the reaction mixture was heated at reflux for 1 h. The reaction mixture was cooled to 0° C., and the reaction was quenched with water (15 mL) and 15% NaOH in water (35 mL). The reaction mixture was filtered, concentrated under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with water and then brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent 1:2 to 3:1 EtOAc/hexanes) provided (3-methanesulfonyl)phenyl methanol as a clear oil (0.56 g, 42%): ¹H NMR (300 MHz, CDCl₃) δ 7.93 (s, 1H), 7.83 (d, J=7 Hz, 1H), 7.64 (d, J=7 Hz, 1H), 7.53 (t, J=7 Hz, 1H), 4.78 (d, J=6 Hz, 2H), 3.05 (s, 3H), 2.61 (br s, 1H).

Step 2. Preparation of 1-chloromethyl-3-methanesulfonylbenzene. A solution of (3-methanesulfonyl)phenyl methanol (0.21 g, 1.1 mmol) in thionyl chloride (3 mL) was heated at 80° C. for 3 h. The reaction mixture was cooled to room temperature, and the solvent was removed under reduced pressure to provide 1-chloromethyl-3-methanesulfonylbenzene as a yellow oil (0.23 g, 95%): ¹H NMR (300 MHz, CDCl₃) δ 7.98 (s, 1H), 7.90 (d, J=8 Hz, 1H), 7.70 (d, J=8 Hz, 1H), 7.59 (t, J=8 Hz, 1H), 4.65 (s, 2H), 3.08 (s, 3H).

Step 3. Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-[(3-methanesulfonyl)-benzyl]-1H-pyridin-2-one. The title compound was prepared by a procedure similar to the one described for Example 80 (0.14 g, 78%): mp 155-157° C.; 1H NMR (300 MHz, CDCl₃) δ 7.88 (d, J=8 Hz, 1H), 7.83 (m, 1H), 7.67 (d, J=8 Hz, 1H), 7.58-7.48 (m, 2H), 7.31 (d, J=8 Hz, 1H), 6.95-6.83 (m, 2H), 6.22 (d, J=8 Hz, 1H), 5.22 (s, 4H), 3.08 (s, 3H). ESHRMS m/z 440.0525 (M+H C₂₀H₁₇ClF₂NO₄S requires 440.0529).

Example 82

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-[(4-methanesulfonyl)benzyl]-1H-pyridin-2-one

The title compound was prepared by a procedure similar to the one described for Example 81 (0.08 g, 73%): mp 223-225° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.91 (d, J=8 Hz, 2H), 7.53-7.47 (m, 3H), 7.30-7.26 (m, 1H), 6.94-6.86 (m, 2H), 6.22 (d, J=8 Hz, 1H), 5.23 (s, 4H), 3.03 (s, 3H). ESHRMS m/z 440.0512 (M+H C₂₀H₁₇ClF₂NO₄S requires 440.0529).

Example 83

Preparation of 4-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzamide

Step 1. Preparation of methyl 4-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzoate. Methyl 4-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzoate was prepared by a procedure similar to the one described for Example 81 (0.14 g, 60%): ¹H NMR (300 MHz, CDCl₃) δ 8.01 (dd, J=8, 2 Hz, 1H), 7.52 (app q, J=8 Hz, 1H), 7.36 (d, J=9 Hz, 2H), 7.26-7.22 (m, 2H), 6.94 (td, J=8, 2 Hz, 1H), 6.85 (td, J=8, 2 Hz, 1H), 6.16 (d, J=9 Hz, 1H), 5.21 (s, 4H), 3.92 (s, 3H).

Step 2. Preparation of 4-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzamide. A sealed tube containing a solution of 4-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzoic acid methyl ester (0.25 g, 0.60 mmol) and NH₃ (20 mL of a 7 N solution in MeOH, 140 mmol) was heated at 75° C. for 16 h. The reaction mixture was cooled to room temperature and the solvent was removed under reduced pressure. Trituration with Et₂O/MeOH afforded 4-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzamide as a white solid (0.14 g, 60%): mp 235-238° C.; ¹H NMR (500 MHz, DMSO-d₆) δ 7.93 (d, J=8 Hz, 2H), 7.79 (d, J=8 Hz, 2H), 7.60 (app q, J=8 Hz, 1H), 7.35-7.27 (m, 4H), 7.20-7.10 (m, 1H), 6.61 (d, J=8 Hz, 1H), 5.28 (s, 2H), 5.14 (s, 2H). ESHRMS m/z 405.0788 (M+H C₂₀H₁₆ClF₂N₂O₃ requires 405.0812).

Example 84

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-isoquinolin-5-ylmethyl-1H-pyridin-2-one

Step 1. Preparation of isoquinolin-5-ylmethanol. To an ice-cold solution of isoquinoline-5-carbaldehyde² (0.68 g, 4.3 mmol) in MeOH (15 mL) was added NaBH₄ (0.17 g, 4.6 mmol), and the reaction mixture was stirred for 15 min. The reaction was quenched with brine, the solvent was removed under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with water and then brine, dried (Na₂SO₄), filtered, and concentrated under reduced pressure to afford isoquinolin-5-ylmethanol as a brown solid (0.63 g, 93%): ¹H NMR (300 MHz, DMSO-d₆) δ 9.87(s, 1H), 8.82 (d, J=6 Hz, 1H), 8.57 (d, J=6 Hz, 1H), 8.47 (d, J=9 Hz, 1H), 8.30 (d, J=6 Hz, 1H), 7.95 (t, J=9 Hz, 1H), 5.34 (s, 2H).

Step 2. Preparation of 5-bromomethylisoquinoline. To a solution of isoquinolin-5-ylmethanol (0.63 g, 3.9 mmol) in AcOH (3.3 mL) was added HBr (6.6 mL, a 30% w/w solution in AcOH, 24 mmol), and the reaction mixture was stirred at 75° C. for 45 min. The reaction mixture was cooled to room temperature, and the precipitate was collected to provide the 5-bromomethylisoquinoline hydrobromide acid salt as a brown solid (1.1 g, 87%): ¹H NMR (300 MHz, CDCl₃) δ 9.22 (s, 1H), 8.58 (d, J=6 Hz, 1H), 7.95-7.89 (m, 2H), 7.76 (d, J=9 Hz, 1H), 7.59 (dd, J=9, 6 Hz, 1H), 5.16 (s, 2H).

Step 3. Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-isoquinolin-5-ylmethyl-1H-pyridin-2-one. The title compound was prepared by a procedure similar to the one described for Example 81, as the TFA salt (0.13 g, 33%): mp 235-238° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 9.55 (s, 1H), 8.66 (d, J=6 Hz, 1H), 8.29 (d, J=6 Hz, 1H), 8.22 (d, J=8 Hz, 1H), 7.91 (d, J=8 Hz, 1H), 7.77 (t, J=8 Hz, 1H), 7.65-7.63 (m, 1H), 7.53 (d, J=7 Hz, 1H), 7.35-7.25 (m, 1H), 7.20-7.10 (m, 1H), 6.68 (d, J=8 Hz, 1H), 5.67 (s, 2H), 5.32 (s, 2H); ¹⁹F NMR (282 MHz, DMSO-d₆) δ −74.79 (3F), −109.43 (1F), −113.62 (1F). ESHRMS m/z 413.0868 (M+H C₂₂H₁₆ClF₂N₂O₃ requires 413.0863).

Example 85

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-(1,2,3,4-tetrahydroisoquinolin-5-ylmethyl)-1H-pyridin-2-one

To a solution of 3-chloro-4-(2,4-difluorobenzyloxy)-1-isoquinolin-5-ylmethyl-1H-pyridin-2-one (Example 84) (0.14 g, 0.34 mmol) in AcOH (1.3 mL) was added NaCNBH₃ (0.09 g, 1.4 mmol), and the reaction mixture was stirred for 2 h. The reaction mixture was cooled to 0° C., and diluted with water (10 mL) and 40% aqueous NaOH (10 mL), and the aqueous layer was washed with EtOAc (3×50 mL). The combined organics were washed with brine, dried (Na₂SO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent 98:1.8:0.2 to 88:10.8:1.2 CH₂Cl₂/MeOH/NH₃) provided 3-chloro-4-(2,4-difluoro-benzyloxy)-1-(1,2,3,4-tetrahydroisoquinolin-5-ylmethyl)-1H-pyridin-2-one as a white solid (0.13 g, 92%): mp 180-184° C.; ¹H NMR (300 MHz, MeOD) δ 7.65-7.55 (m, 2H), 7.16-7.00 (m, 4H), 6.90-6.80 (m, 1H), 6.60 (d, J=8 Hz, 1H), 5.31 (s, 2H), 5.20 (s, 2H), 4.06 (s, 2H), 3.21 (t, J=6 Hz, 2H), 2.82 (t, J=6 Hz, 2H). ESHRMS m/z 417.1173 (M+H C₂₂H₂₀ClF₂N₂O₂ requires 417.1176).

Example 86

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-(1H-indol-5-ylmethyl)-1H-pyridin-2-one

Step 1. Preparation of 5-(Carboxymethyl)-indole-1-carbamic acid tert-butyl ester. To a solution of methyl indole-5-carboxylate (6.9 g, 39 mmol) and Et₃N (6.0 mL, 43 mmol) in CH₂Cl₂ (150 mL) was added di-tert-butyl dicarbonate (19 g, 86 mmol), and the reaction mixture was stirred for 14 h. The reaction mixture was diluted with CH₂Cl₂, washed with water and then brine, dried (Na₂SO₄), filtered, and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica, 3:7 EtOAc/hexanes) provided 5-(Carboxymethyl)-indole-1-carbamic acid tert-butyl ester as a light yellow oil (11 g, 100%): ¹H NMR (300 MHz, CDCl₃) δ 8.29 (s, 1H), 8.15 (d, J=9 Hz, 1H), 7.93 (d, J=9 Hz, 1H), 7.78 (d, J=3 Hz, 1H), 6.85 (d, J=3 Hz, 1H), 3.91 (s, 3H), 1.68 (s, 9H).

Step 2. Preparation of 5-hydroxymethylindole-1-carbamic acid tert-butyl ester. To a −78° C. solution of 5-(Carboxymethyl)-indole-1-carbamic acid tert-butyl ester (10.8 g, 39 mmol) in THF (180 mL) was added DIBAL (127 mL of a 1 M solution in THF, 127 mmol), and the reaction mixture was stirred for 2.5 h. The reaction was quenched with 1:11 N HCl/MeOH (100 mL), the reaction mixture was warmed to room temperature, diluted with CH₂Cl₂ (100 mL), and separated. The organic solution was washed with saturated Rochelle salt, dried (Na₂SO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:1 EtOAc/hexanes) provided 5-hydroxymethylindole-1-carbamic acid tert-butyl ester as a yellow oil (6.5 g, 68%): ¹H NMR (300 MHz, CDCl₃) δ 8.07 (d, J=9 Hz, 1H), 7.59 (d, J=6 Hz, 1H), 7.54 (s, 1H), 7.28 (d, J=9 Hz, 1H), 6.58 (d, J=6 Hz, 1H), 4.73 (s, 2H), 1.97 (s, 9H).

Step 3. Preparation of 5-bromomethylindole-1-carbamic acid tert-butyl ester. To an ice-cold solution of 5-hydroxymethylindole-1-carbamic acid tert-butyl ester (0.51 g, 2.1 mmol) in 4:1 Et₂O/CH₂Cl₂ (4 mL) was added PBr₃ (0.2 mL, 2.2 mmol), and the reaction mixture was stirred for 40 min. The reaction mixture was diluted with CH₂Cl₂, washed a saturated solution of NaHCO₃ (3×10 mL), dried (Na₂SO₄), filtered, and the solvent was removed under reduced pressure to provide 5-bromomethyl-indole-1-carbamic acid tert-butyl ester as a yellow solid (0.59 g, 93%). ¹H NMR (300 MHz, CDCl₃) δ 8.07 (d, J=9 Hz, 1H), 7.68-7.62 (m, 2H), 7.33 (d, J=9 Hz, 1H), 6.60 (s, 1H), 4.68 (s, 2H), 1.67 (s, 9H).

Step 4. Preparation of 5-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]indole-1-carbamic acid tert-butyl ester. 5-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]indole-1-carbamic acid tert-butyl ester was prepared by a procedure similar to the one described for Example 81 as an off-white solid (0.54 g, 67%): ¹H NMR (300 MHz, CDCl₃) δ 8.10 (d, J=8 Hz, 1H), 7.60 (d, J=3 Hz, 2H), 7.52 (m, 1H), 7.26 (m, 1H), 6.94 (td, J=9, 2 Hz, 1H), 6.84 (td, J=9, 2 Hz, 1H) 6.53 (d, J=2 Hz, 1H), 6.08 (d, J=8 Hz, 1H), 5.25 (s, 2H), 5.18 (s, 2H), 1.66 (s, 9H).

Step 5. Preparation of 3-Chloro-4-(2,4-difluorobenzyloxy)-1-(1H-indol-5-ylmethyl)-1H-pyridin-2-one. A flask containing 5-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]indole-1-carbamic acid tert-butyl ester (0.48 g, 0.96 mmol) was heated at 150° C. for 4 h. The reaction mixture was cooled to room temperature, and purification by preparatory HPLC (Phenomenex Luna C18(2) column, 250×21.20 mm, 10 μL Solvent A: 0.05% TFA in 95:5 H₂O/CH₃CN; Solvent B: 0.05% TFA in 95:5 CH₃CN/H₂O; Eluent: 30-95% B over 20 min; flow 20.0 mL/min; UV Detector: 254 nm; Retention Time: 15.6 min) provided 3-chloro-4-(2,4-difluorobenzyloxy)-1-(1H-indol-5-ylmethyl)-1H-pyridin-2-one as an off-white solid (0.14 g, 36%): mp 152-153° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 11.11 (br s, 1H), 7.91 (d, J=8 Hz, 1H), 7.61 (app q, J=8 Hz, 1H, 7.51 (s, 1H), 7.36-7.33 (m, 3H), 7.16 (td, J=8, 2 Hz, 1H), 7.09 (dd, J=8, 2 Hz, 1H), 6.57 (d, J=8 Hz, 1H), 6.40 (br s, 1H), 5.28 (s, 2H), 5.16 (s, 2H). ESHRMS m/z 401.0845 (M+H C₂₁H₁₆ClF₂N₂O₂ requires 401.0863).

Example 87

Preparation of 1-(1-acetyl-1H-indol-5-ylmethyl)-3-chloro-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

To a solution of 3-chloro-4-(2,4-difluorobenzyloxy)-1-(1H-indol-5-ylmethyl)-1H-pyridin-2-one (Step 5, synthesis of Example 86) (0.22 g, 0.57 mmol) in CH₃CN (10 mL) was added acetic anhydride (0.06 mL, 0.58 mmol) and Et₃N (2 mL), and the reaction mixture was stirred at 86° C. for 6 h. The reaction mixture was cooled to room temperature, and partitioned between 1 N HCl and EtOAc. The organic solution was separated, washed with brine, dried (Na₂SO₄), filtered, and concentrated under reduced pressure. ¹H NMR (300 MHz, MeOD) δ 8.35 (d, J=9 Hz, 1H), 7.77 (d, J=9 Hz, 1H), 7.70 (d, J=3 Hz, 1H), 7.54 (s, 2H), 7.31 (d, J=9 Hz, 1H), 7.01-6.99 (m, 2H), 6.66 (d, J=3 Hz, 1H), 6.59 (d, J=9 Hz, 1H), 5.29 (s, 4H), 2.63 (s, 3H). ESHRMS m/z 443.0965 (M+H C₂₃H₁₈ClF₂N₂O₃ requires 443.0969).

Example 88

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-(2,3-dihydro-1H-indol-5-ylmethyl)-1H-pyridin-2-one

To a solution of 3-chloro-4-(2,4-difluorobenzyloxy)-1-(1H-indol-5-ylmethyl)-1H-pyridin-2-one (Step 5, synthesis of Example 86) (0.24 g, 0.60 mmol) in AcOH (5 mL) was added NaCNBH₃ (0.06 g, 1.0 mmol), and the reaction mixture was stirred for 1 h. The reaction mixture was partitioned between water and EtOAc, and the precipitate was collected by filtration. Trituration with CH₂Cl₂ afforded 3-Chloro-4-(2,4-difluorobenzyl-oxy)-1-(2,3-dihydro-1H-indol-5-ylmethyl)-1H-pyridin-2-one as a white solid (0.2 g, 81%): mp 137-139° C.; 1H NMR (300 MHz, CDCl₃) δ 7.51 (app q, J=9 Hz, 1H), 7.21 (d, J=6 Hz, 1H), 7.11 (s, 1H), 6.99-6.80 (m, 3H), 6.57 (d, J=9 Hz, 1H), 6.08 (d, J=9 Hz, 1H), 5.18 (s, 2H), 5.02 (s, 2H), 3.83 (br s, 1H), 3.55 (t, J=9 Hz, 2H), 2.99 (t, J=9 Hz, 2H). ESHRMS m/z 403.1022 (M+H C₂₁H₁₈ClF₂N₂O₂ requires 403.1019).

The following example compounds were prepared by procedures similar to that described for Example 74. The yields and the analytical data of the title compounds are reported below.

Examples 89-101

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 89-101 are prepared essentially according to the procedures set forth above for Example 74. The yield (Y), molecular formula (MF) and analytical data for these compounds are shown below.

Example				M + H	ESHRMS
No.	R	Y	MF	Requires	m/z
Ex. 89	pyridin-3-ylmethyl	25	C18H13BrF2N2O2	407.0202	407.0197
Ex. 90	pyridin-4-ylmethyl	6	C18H13BrF2N2O2	407.0202	407.0189
Ex. 91	pyridin-2-ylmethyl	56	C18H13BrF2N2O2	407.0201	407.0184
Ex. 92	4-tert-butyl)benzyl	32	C23H22BrF2NO2	462.0875	462.0863
Ex. 93	3-methoxybenzyl	50	C20H16BrF2NO3	436.0354	436.0353
Ex. 94	Benzo[1,3]dioxol-5-ylmethyl	35	C20H14BrF2NO4	450.0147	450.0136
Ex. 95	2-fluorobenzyl	42	C19H14BrF3NO2	424.0155	424.0143

Example 96

Preparation of 3-bromo-4-(2,4-difluorobenzyloxy)-1-(2,4-difluorobenzyl)-1H-pyridin-2-one

Step 1. Preparation of 4-(2,4-difluorobenzyloxy)-1-(2,4-difluorobenzyl)-1H-pyridin-2-one. To a solution of 2,4-dihydroxypyridine (0.35 g, 3.2 mmol) in DMF (50 mL) was added K₂CO₃ (2.5 g, 13 mmol) and 2,4-difluorobenzyl bromide (1.0 mL, 7.6 mmol), and the reaction mixture was stirred at 110° C. for 4 h. The reaction mixture was cooled to room temperature, diluted with brine, and extracted with CHCl₃ (4×100 mL). The combined organics were washed with water and then brine, dried (Na₂SO₄), filtered, and concentrated under reduced pressure. ¹H NMR (300 MHz, CDCl₃) δ 7.54 (app q, J=8 Hz, 1H), 7.38-7.28 (m, 5H), 6.94 (td, J=8, 2 Hz, 1H), 6.85 (td, J=8, 2 Hz, 1H), 6.10 (d, J=9 Hz, 1H), 5.21 (s, 2H), 5.16 (s, 2H), 4.56 (s, 2H).

Step 2. Preparation of 3-Bromo-4-(2,4-difluorobenzyloxy)-1-(2,4-fluorobenzyl)-1H-pyridin-2-one. To an ice-cold solution of 4-(2,4-difluorobenzyloxy)-1-(2,4-difluorobenzyl)-1H-pyridin-2-one (0.72 g, 2.0 mmol) in AcOH (4.0 mL) was added a solution of bromine (0.11 mL, 2.2 mmol) in AcOH (7.2 mL), and the reaction mixture was stirred for 40 min. The solvent was removed under reduced pressure. ¹H NMR (300 MHz, CDCl₃) δ 7.63-7.45 (m, 2H), 7.42 (d, J=6 Hz, 1H), 6.93-6.77 (m, 4H), 6.12 (d, J=6 Hz, 1H), 5.20 (s, 2H), 5.12 (s, 2H). ERMS m/z M+H 442.

Example 97

Preparation of {3-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}acetonitrile

Step 1. Preparation of methyl 3-cyanomethylbenzoate. To an ice-cold solution of methyl 3-bromomethylbenzoate (9.1 g, 40 mmol) in CH₃CN (108 mL) was added tetrabutylammonium fluoride (17.3 mL, 60 mmol) and trimethylsilylcyanide (8.0 mL, 60 mmol), and the reaction mixture was heated at reflux for 20 h. The reaction mixture was cooled to room temperature, and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica, 1:1 EtOAc/hexanes) provided methyl 3-cyanomethylbenzoate as a clear oil (3.0 g, 43%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.97 (s, 1H), 7.92 (d, J=8 Hz, 1H), 7.64 (d, J=8 Hz, 1H), 7.56 (t, J=8 Hz, 1H), 4.16 (s, 2H), 3.87 (s, 3H).

Step 2. Preparation of (3-hydroxymethylphenyl)acetonitrile. To an ice-cold solution of methyl 3-cyanomethylbenzoate (2.8 g, 18 mmol) in THF (23 mL) was added LiBH₄ (8.8 mL of a 2 M solution in THF, 18 mmol), and the reaction mixture was heated at reflux for 4 h. The reaction mixture was cooled to room temperature, the reaction was quenched with 1:1 water/I N HCl, and the aqueous layer was washed with EtOAc (3×150 mL). The combined organics were washed with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 2:1 EtOAc/hexanes) provided (3-hydroxymethylphenyl)-acetonitrile as a clear oil (0.97 g, 41%): ¹H NMR (300 MHz, MeOD) δ 8.15-8.08 (m, 1H), 7.47-7.34 (m, 1H), 7.27 (s, 1H), 6.97-6.82 (m, 1H), 4.87 (s, 2H), 3.91 (s, 2H).

Step 3. Preparation of (3-bromomethylphenyl)acetonitrile. To an ice-cold solution of (3-hydroxymethylphenyl)acetonitrile (0.97 g, 7.3 mmol) in THF (35 mL) was added CBr₄ (2.5 g, 7.7 mmol) and Ph₃P (2.0 g, 7.7 mmol), and the reaction mixture was stirred for 3 h. The reaction mixture was filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent 1:9 to 1:4 EtOAc/hexanes) provided (3-bromomethylphenyl)acetonitrile as a clear oil (0.89 g, 58%): ¹H NMR (300 MHz, MeOD) δ 7.47-7.29 (m, 1H), 7.27 (s, 1H), 6.97-6.82 (m, 1H), 4.87 (s, 2H), 3.91 (s, 2H).

Step 4. Preparation of {3-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]phenyl}acetonitrile. The title compound was prepared by a procedure similar to the one described for Example 74 (0.07 g, 10%): mp 120-121° C.; 1H NMR (300 MHz, CDCl₃) δ 7.60-7.50 (m, 1H), 7.37-7.27 (m, SH), 6.96 (td, J=9, 3 Hz, 1H), 6.82 (td, J=9, 3 Hz, 1H), 6.13 (d, J=8 Hz, 1H), 5.21 (s, 2H), 5.16 (s, 2H). ESHRMS m/z 445.0381 (M+H C₂₁H₁₆BrF₂N₂O₂ requires 445.0358).

Example 98

Preparation of 2-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzonitrile

The title compound was prepared by a procedure similar to the one described for Example 74 (0.13 g, 47%): mp 194-197° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.75 (d, J=9 Hz, 1H), 7.69-7.49 (m, 4H), 7.42 (t, J=8 Hz, 1H), 6.96-6.73 (m, 2H), 6.18 (d, J=8 Hz, H), 6.17 (s, 2H), 5.30 (s, 2H). ESHRMS m/z 431.0210 (M+H C₂₀H₁₄BrF₂N₂O₂ requires 431.0201.

Example 99

Preparation of 1-[(2-aminomethyl)benzyl)]-3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

To a solution of 2-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzonitrile (0.11 g, 0.25 mmol) in THF (3 mL) was added BH₃.DMS (0.25 mL of a 2.0 M solution in THF, 0.5 mmol), and the reaction mixture was stirred at 70° C. for 1 h. The reaction mixture was cooled to 0° C., and the reaction was quenched with MeOH. The solvent was removed under reduced pressure, and the residue was partitioned between 2N NaOH and EtOAc. The organic solution was washed with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent methylene chloride to 90:9:1 methylene chloride/methanol/ammonia) provided 1-[(2-aminomethyl)benzyl]-3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one as a white solid (0.15 g, 48%): ¹H NMR (300 MHz, CDCl₃) δ 7.55 (app q, J=8 Hz, 1H), 7.40-7.26 (m, 4H), 7.14 (d, J=8 Hz, 1H), 6.94 (td, J=8, 2 Hz, 1H), 6.85 (td, J=8, 2 Hz, 1H), 6.08 (d, J=8 Hz, 1H), 5.31 (s, 2H), 5.21 (s, 2H) 4.03 (s, 2H). ESHRMS m/z 435.0517 (M+H C₂₀H₁₈BrF₂N₂O₂ requires 435.0514).

Example 100

Preparation of Methyl 3-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzoate

The title compound was prepared by a procedure similar to the one described for Example 74 (0.05 g, 11%): mp 115-117° C.; ¹H NMR (300 MHz, CDCl₃) δ 8.15-7.95 (m, 2H), 7.65-7.50 (m, 2H), 7.45-7.40 (m, 1H), 7.32 (d, J=6 Hz, 1H), 7.00-6.80 (m, 2H), 6.12 (d, J=9 Hz, 1H), 5.21 (s, 2H), 5.20 (s, 2H), 3.92 (s, 3H). ESHRMS m/z 464.0292 (M+H C₂₁H₁₇BrF₂NO₄ requires 464.0303).

Example 101

Preparation of Methyl 4-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-benzoate

The title compound was prepared by a procedure similar to the one described for Example 74 (0.17 g, 46%): mp 136-139° C.; ¹H NMR (300 MHz, CDCl₃) δ 8.01 (d, J=8 Hz, 2H), 7.60-7.51 (m, 1H), 7.37 (d, J=8 Hz, 2H), 7.29-7.26 (m, 1H), 6.93 (td, J=9, 2 Hz, 1H), 6.84 (td, J=9, 2 Hz, 1H), 6.13 (d, J=8 Hz, 1H), 5.23 (s, 4H), 3.91 (s, 3H). ESHRMS m/z 464.0306 (M+H C₂₁H₁₇BrF₂NO₂ requires 464.0304).

Example 102

Preparation of 3-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzamide

A sealed tube containing a solution of methyl 3-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzoate (0.1 g, 0.21 mmol) and NH₃ (3 mL of a 7 N solution in MeOH, 21 mmol) was heated at 75° C. for 16 h. The reaction mixture was cooled to room temperature and the solvent was removed under reduced pressure. Trituration with Et₂O/MeOH afforded a white solid (0.06 g, 64%): mp 198-201° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 8.02-8.00 (m, 2H), 7.85-7.75 (m, 2H), 7.70-7.60 (m, 1H), 7.45-7.30 (m, 4H), 7.17 (t, J=3 Hz, 1H), 6.60 (d, J=9 Hz, 1H), 5.32 (s, 2H), 5.18 (s, 2H). ESHRMS m/z 449.0295 (M+H C₂₀H₁₆BrF₂N₂O₃ requires 449.0307).

Example 103

Preparation of 4-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]benzamide

The title compound was prepared by a procedure similar to the one described for Example 102 from Example 101 (0.04 g, 12%): mp 235-238° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 8.00 (d, J=8 Hz, 1H), 7.94 (br s, 1H), 7.78 (d, J=8 Hz, 1H), 7.64 (app q, J=8 Hz, 1H), 7.38-7.30 (m, 4H), 7.17 (td, J=6, 2 Hz, 1H), 6.60 (d, J=9 Hz, 1H), 5.27 (s, 2H), 5.14 (s, 2H). ESHRMS m/z 449.0291 (M+H C₂₀H₁₆BrF₂N₂O₃ requires 449.0307).

Example 104

Preparation of 1-(3-aminomethyl-2-fluorobenzyl)-3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

Step 1. Preparation of 3-Bromo-1-(3-bromomethyl-2-fluorobenzyl)-4-(2,4-difluoro-benzyloxy)-1H-pyridin-2-one. To a solution of 3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one (from Step 3, Example 74) (0.3 g, 0.95 mmol) in DMF (26 mL) was added K₂CO₃ (0.26 g, 1.9 mmol) and 2,6-bis(bromomethyl)fluorobenzene (1.6 g, 5.7 mmol), and the reaction mixture was stirred at 110° C. for 3 h. The reaction mixture was cooled to room temperature, and the solvent was removed under reduced pressure. The residue was diluted with a 50% aqueous solution of brine, and the aqueous layer was extracted with EtOAc (3×50 mL). The combined organics were washed with water, dried (Na₂SO₄), filtered, and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica, eluent 99:1 to 95:5 methylene chloride/methanol) afforded 3-bromo-1-(3-bromomethyl-2-fluorobenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one as an off-white solid (0.24 g, 49%): ¹H NMR (300 MHz, CDCl₃) δ 7.55-7.40 (m, 3H), 7.35-7.25 (m, 1H), 7.10-7.05 (m, 1H), 7.00-6.80 (m, 2H), 6.14 (d, J=6 Hz, 1H), 5.22 (s, 2H), 5.19 (s, 2H), 4.50 (s, 2H).

Step 2. Preparation of 1-(3-aminomethyl-2-fluorobenzyl)-3-bromo-4-(2,4-difluoro-benzyloxy)-1H-pyridin-2-one. A sealed tube containing a solution of 3-bromo-1-(3-bromomethyl-2-fluorobenzyl)-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one (0.24 g, 0.45 mmol) and NH₃ (24 mL of a 7 N solution in MeOH, 168 mmol) was heated at 80° C. for 1 h. The reaction mixture was cooled to room temperature and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica, eluent 99.5:0.5 to 96:4 methylene chloride/methanol) afforded a white solid (0.12 g, 60%): mp 160-163° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.46-7.45 (m, 1H), 7.44-7.35 (m, 2H), 7.34-7.26 (m, 1H), 7.15-7.05 (m, 1H), 6.95-6.80 (m, 2H), 6.11 (d, J=9 Hz, 1H), 5.21 (s, 2H), 5.19 (s, 2H), 3.90 (s, 2H). ESHRMS m/z 453.0442 (M+H C₂₀H₁₇BrF₃N₂O₂ requires 453.0420).

Example 105

Preparation of Methyl 3-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-2-fluoro-benzoate

Step 1. Preparation of methyl 2-fluoro-3-methylbenzoate. To a solution of 2-fluoro-3-methyl benzoic acid (3.57 g, 23 mmol) in MeOH (40 mL) was added concentrated sulfuric acid (2.3 mL), and the reaction mixture was heated at reflux for 12 h. The reaction mixture was cooled, the solvent was removed under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with a saturated solution of NaHCO₃ and then brine, dried (Na₂SO₄), filtered and concentrated under reduced pressure to afford methyl 2-fluoro-3-methylbenzoate as a yellow oil (3.2 g, 82%): ¹H NMR (300 MHz, CDCl₃) δ 7.76-7.71 (m, 1H), 7.39-7.34 (m, 1H), 7.08 (t, J=8 Hz, 1H), 3.98 (s, 3H), 2.31 (d, J=3 Hz, 3H).

Step 2. Preparation of methyl 3-bromomethyl-2-fluorobenzoate. To a mixture of methyl 2-fluoro-3-methylbenzoate (1.5 g, 8.9 mmol) and N-bromosuccinimide (1.67 g, 9.4 mmol) was added carbon tetrachloride (24 mL) and benzoyl peroxide (5 mg), and the mixture was heated at reflux for 16 h. The reaction mixture was cooled, filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent 5:95 to 60:40 EtOAc/hexanes) afforded methyl 3-bromomethyl-2-fluorobenzoate as a light yellow solid (0.91 g, 41%): ¹H NMR (300 MHz, CDCl₃) δ 7.93-7.88 (m, 1H), 7.61-7.56 (m, 1H), 7.20 (t, J=8 Hz, 1H), 4.53 (d, J=3 Hz, 2H), 3.94 (s, 3H).

Step 3. Preparation of Methyl 3-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-2-fluorobenzoate. Methyl 3-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-2-fluorobenzoate was prepared by a procedure similar to the one described for Example 81 (0.33 g, 69%): mp 171-174° C.; 1H NMR (300 MHz, CDCl₃) δ 7.89-7.84 (m, 2H), 7.60-7.45 (m, 2H), 7.25-7.15 (m, 1H), 7.00-6.80 (m, 2H), 6.17 (d, J=6.0 Hz, 1H), 5.21 (s, 2H), 5.19 (s, 2H), 3.93 (s, 3H). ESHRMS m/z 438.0747 (M+H C₂₁H₁₆ClF₃NO₄ requires 438.0714).

Example 106

Preparation of 3-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-2-fluoro-benzamide

The title compound was prepared by a procedure similar to the one described for Example 99 (0.15 g, 62%): mp 252-254° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 8.04 (d, J=8 Hz, 1H), 7.92 (br s, 1H), 7.79-7.65 (m, 3H), 7.49-7.48 (m, 1H), 7.37-7.31 (m, 3H), 6.80 (d, J=8 Hz, 1H), 5.46 (s, 2H), 5.33 (s, 2H). ESHRMS m/z 423.0710 (M+H C₂₀H₁₅ClF₃N₂O₃ requires 423.0718).

Example 107

Preparation of 3-bromo-4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one

Step 1. Preparation of 4-Benzyloxy-1-(3-fluorobenzyl)-1H-pyridin-2-one. To a solution of 4-benzyloxy-1H-pyridin-2-one (1.0 g, 5 mmol) and K₂CO₃ (2.0 g, 9.9 mmol) in DMF (30 mL) was added 3-fluorobenzyl bromide (1.4 g, 7.5 mmol), and the reaction mixture was heated to 110° C. for 3 h. The reaction mixture was cooled to room temperature, and partitioned between EtOAc and water. The organic solution was washed with water and then brine, dried (Na₂SO₄), filtered and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent 97:3 to 93:7 methylene chloride/methanol) afforded 4-benzyloxy-1-(3-fluorobenzyl)-1H-pyridin-2-one (1.04 g, 67%): ¹H NMR (300 MHz, CDCl₃) δ 7.45-7.25 (m, 5H), 7.13 (d, J=8 Hz, 1H), 7.10-6.90 (m, 3H), 6.10-5.95 (m, 2H), 5.07 (s, 2H), 5.00 (s, 2H).

Step 2. Preparation of 1-(3-Fluorobenzyl)-4-hydroxy-1H-pyridin-2-one. To a solution of 4-benzyloxy-1-(3-fluorobenzyl)-1H-pyridin-2-one (1.79 g, 5.8 mmol) in EtOH (50 mL) was added 10% Pd/C (0.4 g), and reaction mixture was stirred under a hydrogen atmosphere for 1.5 h. The reaction mixture was filtered through diatomaceous earth and concentrated under reduced pressure to give 1-(3-fluorobenzyl)-4-hydroxy-1H-pyridin-2-one (0.92 g, 72%): ¹H NMR (300 MHz, CDCl₃) δ 7.55 (d, J=6 Hz, 1H), 7.40-7.30 (m, 1H), 7.10-6.95 (m, 3H), 6.07 (dd, J=6, 3 Hz, 1H), 5.85 (d, J=3 Hz, 1H), 5.11 (s, 2H).

Step 3. Preparation of 3-Bromo-1-(3-fluorobenzyl)-4-hydroxy-1H-pyridin-2-one. To an ice-cold solution of 1-(3-fluorobenzyl)-4-hydroxy-1H-pyridin-2-one (0.67 g, 3.1 mmol) in AcOH (5.7 mL) was added a solution of bromine (0.52 g, 3.24 mmol) in AcOH (10.8 mL), and the reaction mixture was stirred for 5 min. The reaction mixture was warmed to room temperature and concentrated under reduced pressure to afford 3-bromo-1-(3-fluorobenzyl)-4-hydroxy-1H-pyridin-2-one as a yellow solid (1.07 g, crude): ¹H NMR (500 MHz, MeOD) δ 7.64 (d, J=8 Hz, 1H), 7.35-7.30 (m, 1H), 7.05-6.90 (m, 3H), 6.20 (d, J=8 Hz, 1H), 5.18 (s, 2H).

Step 4. Preparation of 3-Bromo-4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one. To a solution of 3-bromo-1-(3-fluorobenzyl)-4-hydroxy-1H-pyridin-2-one (0.20 g, 0.67) and K₂CO₃ (0.27 g, 1.34 mmol) in acetone (10 mL) was added 2,4-difluorobenzyl bromide (0.16 g, 0.8 mmol), and the reaction mixture was heated at reflux for 1 h. The reaction mixture was cooled to room temperature, concentrated under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with water and then brine, dried (Na₂SO₄), filtered and concentrated under reduced pressure. ¹H NMR (300 MHz, CDCl₃) δ 7.65-7.55 (m, 1H), 7.40-7.25 (m, 2H), 7.15-6.80 (m, 5H), 6.14 (d, J=8 Hz, 1H), 5.22 (s, 2H), 5.16 (s, 2H). ESHRMS m/z 424.0159 (M+H Cl₉H₁₄BrF₃NO₂ requires 424.0155).

Example 108

Preparation of 3-bromo-1-(3-fluorobenzyl)-4-(2,3,4-trifluorobenzyloxy)-1H-pyridin-2-one

The title compound was prepared by a procedure similar to the one described for Example 107 (0.09 g, 39%): mp 176-178° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.40-7.25 (m, 4H), 7.11-6.98 (m, 4H), 6.11 (d, J=9 Hz, 1H), 5.23 (s, 2H), 5.16 (s, 2H). ESHRMS m/z 442.0060 (M+H C₁₉H₁₃BrF₄NO₂ requires 442.0061).

Example 109

Preparation of 1-[3-(2-Aminoethyl)benzyl]-3-bromo-4-(2,4-difluorobenzyloxy)-1H-pyridin-2-one

The title compound was prepared from compound of Example 97 by a procedure similar to the one described for Example 99, as the TFA salt (0.13 g, 33%): mp 70-74° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 8.21 (br s, 1H), 6.60-6.50 (m, 1H), 7.52 (d, J=6 Hz, 1H), 7.30-7.10 (m, 3H), 7.01 (d, J=9 Hz, 1H), 6.94-6.85 (m, 2H), 6.20 (d, J=6 Hz, 1H), 5.20 (s, 2H), 5.05 (s, 2H), 3.23 (br s, 2H), 2.97 (t, J=8 Hz, 2H), 2.05 (br s, 2H). ESHRMS m/z 449.0698 (M+H C₂₁H₂₀BrF₂N₂O₂ requires 449.0671).

Example 110

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one

Step 1. Preparation of 4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one. To a solution of 1-(3-fluorobenzyl)-4-hydroxy-1H-pyridin-2-one (from Step 2 EXAMPLE 107) (0.92 g, 4.2 mmol) and K₂CO₃ (1.2 g, 8.4 mmol) in acetone (62 mL) was added 2,4-difluorobenzyl bromide (1.3 g, 6.3 mmol), and the reaction mixture was heated at reflux for 3 h. The reaction mixture was cooled room temperature, concentrated under reduced pressure, and the residue was partitioned between water and EtOAc. The organic solution was washed with brine, dried (Na₂SO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent methylene chloride to 95:5 methylene chloride/methanol) to provide 4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one as a white solid (1.21 g, 84%): ¹H NMR (300 MHz, CDCl₃) δ 7.45-7.20 (m, 2H), 7.14 (d, J=8 Hz, 1H), 7.05-6.75 (m, 5H), 6.05 (d, J=3 Hz, 1H), 5.95 (dd, J=5, 3 Hz, 1H), 5.08 (s, 2H), 5.00 (s, 2H).

Step 2. Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one. To a solution of 4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one (0.15 g, 0.4 mmol) in AcOH (3 mL) was added N-chlorosuccinimide (70 mg, 0.5 mmol), and the reaction mixture was heated at reflux for 10 min. The reaction mixture was cooled room temperature and the solvent was removed under reduced pressure. ¹H NMR (300 MHz, CDCl₃) δ 7.60-7.50 (m, 1H), 7.45-7.20 (m, 2H), 7.10-6.80 (m, 5H), 6.16 (d, J=8 Hz, 1H), 5.21 (s, 2H), 5.15 (s, 2H). ESHRMS m/z 380.0641 (M+H C₁₉H₁₄ClF₃NO₂ requires 480.0660).

The following example compounds were prepared by procedures similar to that described for Example 107. The yields and the analytical data are described below.

Example 111

Preparation of 3-bromo-4-(3-chlorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one

The title compound was prepared by a procedure similar to the one described for EXAMPLE 107 (0.12 g, 42%): mp 149-153° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.40-7.23 (m, 6H), 7.09 (d, J=8 Hz, 1H), 7.05-6.95 (m, 2H), 6.05 (d, J=8 Hz, 1H), 5.19 (s, 2H), 5.14 (s, 2H). ESMS m/z M+H 442.

Example 112

Preparation of 3-bromo-4-(3,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one

The title compound was prepared by a procedure similar to the one described for EXAMPLE 107 (0.08 g, 48%): mp 172-174° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.40-6.95 (m, 8H), 6.05 (d, J=6 Hz, 1H), 5.16 (s, 4H). ESHRMS m/z 424.0111 (M+H C₁₉H₁₄BrF₃NO₂ requires 424.0155).

Example 113

Preparation of 3-bromo-1-(3-fluorobenzyl)-4-(4-fluorobenzyloxy)-1H-pyridin-2-one

The title compound was prepared by a procedure similar to the one described for EXAMPLE 107 (0.07 g, 35%): mp 180-183° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.50-7.25 (m, 5H), 7.15-7.00 (m, 4H), 6.07 (d, J=8 Hz, 1H), 5.18 (s, 2H), 5.14 (s, 2H). ESHRMS m/z 406.0258 (M+H C₁₉H₁₅BrF₂NO₂ requires 406.0249).

Example 114

Preparation of 3-bromo-1-(3-fluorobenzyl)-4-(3-fluorobenzyloxy)-1H-pyridin-2-one

To an ice-cold solution of 1-(3-fluorobenzyl)-4-(3-fluorobenzyloxy)-1H-pyridin-2-one (0.14 g, 0.43 mmol) in AcOH (2 mL) was added a solution of bromine (72 mg, 0.45 mmol) in AcOH (1 mL), and the reaction mixture was stirred for 5 min. The reaction mixture was warmed to room temperature and the solvent was removed under reduced pressure. ¹H NMR (300 MHz, CDCl₃) δ 7.45-6.95 (m, 9H), 6.05 (d, J=8 Hz, 1H), 5.21 (s, 2H), 5.14 (s, 2H). ESHRMS m/z 406.0254 (M+H C₁₉H₁₅BrF₂NO₂ requires 406.0249).

Examples 115-123

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 115-123 are prepared essentially according to the procedures set forth above for Example 107

Example			M + H	ESHRMS
No.	R	MF	Requires	m/z
Ex. 115	3-methoxy	C20H17BrFNO3	418.0449	418.0427
Ex. 116	4-tert-butyl	C23H23BrFNO2	444.0969	444.0977
Ex. 117	3-methyl	C20H17BrFNO2	402.0499	402.0513
Ex. 118	4-trifluoromethyl	C20H14BrF4NO2	456.0217	456.0210
Ex. 119	4-cyano	C20H14BrFN2O2	413.0295	413.0313
Ex. 120	2-methyl	C20H17BrFNO2	402.0499	402.0502
Ex. 121	2-phenyl	C25H19BrFNO2	464.0656	464.0654
Ex. 122	4-methoxy	C20H17BrFNO3	418.0449	418.0455
Ex. 123	2-CO2CH3	C21H17BrFNO4	446.0398	446.0403

NMR characterization of compounds of Examples 115-123

Example # NMR Data
Ex. 115   1H NMR (300MHz, CDCl3) δ 7.35-7.20(m, 4H), 7.15-6.85(m, 5H), 6.07(d, J=8Hz,
          1H), 5.21(s, 2H), 5.13(s, 2H), 3.82(s, 3H)
Ex. 116   1H NMR (300MHz, CDCl3) δ 7.45-7.20(m, 4H), 7.10-6.95(m, 3H), 6.11(d, J=8Hz,
          1H), 5.19(s, 2H), 5.14(s, 2H), 1.32(s, 9H)
Ex. 117   1H NMR (300MHz, CDCl3) δ 7.40-6.90(m, 9H), 6.08(d, J=8Hz, 1H), 5.19(s, 2H), 5.14
          (s, 2H), 2.37(s, 3H)
Ex. 118   1H NMR (300MHz, CDCl3) δ 7.67-7.53(m, 4H), 7.31-724(m, 2H), 7.09-6.98(m, 3H),
          6.04(d, J=8Hz, 1H), 5.26(s, 2H), 5.14(s, 2H)
Ex. 119   1H NMR (300MHz, CDCl3) δ 7.71(dd, J=8, 2Hz, 2H), 7.58-7.55(m, 2H), 7.29-7.25(m,
          2H), 7.09(d, J=8Hz, 1H), 7.03-6.98(m, 2H), 6.03(dd, J=8, 2Hz, 1H), 5.26(s, 2H),
          5.15(s, 2H)
Ex. 120   1H NMR (300MHz, CDCl3) δ 7.45-6.90(m, 9H), 6.15-6.10(m, 1H), 5.18(s, 2H), 5.15(s,
          2H), 2.38(s, 3H)
Ex. 121   1H NMR (300MHz, CDCl3) δ 7.70-7.65(m, 1H), 7.55-7.25(m, 9H) 7.14(d, J=8Hz,
          1H), 7.10-6.95(m, 3H), 5.81(d, J=8Hz, 1H), 5.12(s, 2H), 5.08(s, 2H)
Ex. 122   1H NMR (300MHz, CDCl3) δ 7.40-7.25(m, 3H), 7.15-6.90(m, 6H), 6.15-6.10(m, 1H),
          5.16(s, 2H), 5.14(s, 2H), 3.82(s, 3H)
Ex. 123   1H NMR (300MHz, CDCl3) δ 8.06(dd, J=8, 1Hz, 1H), 7.87(d, J=8Hz, 1H), 7.70-7.60-
          (m, 1H), 7.50-7.25(m, 3H), 7.09(d, J=8Hz, 1H), 7.05-6.95(m, 2H), 6.19(d, J=8Hz,
          1H), 5.65(s, 2H), 5.16(s, 2H), 3.91(s, 3H)

Example 124

Preparation of 3-Bromo-1-(3-fluorobenzyl)-4-(2-hydroxymethylbenzyloxy)-1H-pyridin-2-one

Step 1. Preparation of 3-Bromo-1-(3-fluorobenzyl)-4-(2-hydroxymethylbenzyloxy)-1H-pyridin-2-one.

To an ice-cold solution of methyl 2-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydro-pyridin-4-yloxymethyl]benzoate (0.12 g, 0.28 mmol) in THF (5 mL) was added LiBH₄ (0.15 mL of a 2.0 M solution in THF, 0.30 mmol), and the reaction mixture heated at reflux for 5 hours. The reaction mixture was cooled to room temperature, the solvent was removed under reduced pressure, and the residue dissolved in EtOAc. The organic solution was washed with brine, dried (Na₂SO₄), filtered, and concentrated under reduced pressure. ¹H NMR (300 MHz, DMSO-d₆) δ 7.98 (d, J=8 Hz, 1H), 7.46-7.28 (m, 5H), 7.15-7.10 (m, 3H), 6.56 (d, J=8 Hz, 1H), 5.35 (s, 2H), 5.25 (br s, 1H), 5.14 (s, 2H). ESHRMS m/z 418.0453 (M+H C₂₀H₁₈BrFNO₃ requires 418.0449).

Example 126

Preparation of 2-{2-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}acetamide

Example 126

Step 1. Preparation of (2-Bromomethylphenyl)acetic Acid.

A solution of isochroman-3-one (1.5 g, 10 mmol) in 30% HBr in acetic acid (13 mL) was stirred at room temperature for 2 h, and 70° C. for 1 h. The reaction mixture was cooled to room temperature, and poured into ice-water. The precipitate was collected to afford (2-bromomethylphenyl)acetic acid as an off-white solid (2.15 g, 93%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.45-7.23 (m, 4H), 4.73 (s, 2H), 3.73 (s, 2H).

Step 2. Preparation of Methyl(2-Bromomethylphenyl)acetate.

To an ice-cold solution of (2-bromomethylphenyl)acetic acid (1 g, 4.4 mmol) in THF (2.4 mL) was added trimethylsilyldiazomethane (3 mL of a 2 M solution in hexanes, 6 mmol), and the reaction mixture was stirred for 14 h. The reaction was quenched with AcOH, and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica, eluent 98:2 to 94:6 methylene chloride/hexanes) afforded methyl (2-bromomethylphenyl)acetate as a light yellow solid (0.34 g, 32%): ¹H NMR (300 MHz, CDCl₃) δ 7.40-7.20 (m, 4H), 4.59 (s, 2H), 3.81 (s 2H), 3.71 (s, 3H).

Step 3. Preparation of Methyl {2-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]phenyl}acetate.

Methyl {2-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}acetate was prepared by a procedure similar to the one described for EXAMPLE 74 (0.41 g, 68%): ¹H NMR (300 MHz, CDCl₃) δ 7.55-6.81 (m, 8H), 6.10 (d, J=6 Hz, 1H), 5.20 (s, 4H), 3.78 (s, 2H), 3.60 (s, 3H).

Step 4. Preparation of 2-{2-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]phenyl}acetamide.

2-{2-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]phenyl}-acetamide was prepared by a procedure similar to the one described for Example 102 (0.07 g, 72%): mp 178-183° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 7.89 (d, J=8 Hz, 1H), 7.66 (d, J=9 Hz, 1H), 7.54 (br s, 1H), 7.35 (br s, 1H), 7.30-7.15 (m, 4H), 6.98 (br s, 1H), 6.85 (d, J=7 Hz, 1H), 6.60 (d, J=8 Hz, 1H), 5.32 (s, 2H), 5.19 (s, 2H), 3.62 (s, 2H). ESHRMS m/z 463.0442 (M+H C₂₁H₁₈BrF₂N₂O₃ requires 463.0463).

Example 127

Preparation of Ethyl {3-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]-phenyl}acetate

Example 127

Step 1. Preparation of Ethyl(3-bromomethylphenyl)acetate.

To a mixture of m-tolylacetic acid ethyl ester (3.0 g, 16.8 mmol) and N-bromosuccinimide (3.0 g, 16.8 mmol) was added carbon tetrachloride (45 mL), followed by benzoyl peroxide (5 mg), and the reaction mixture was heated at reflux for 16 h. The reaction mixture was cooled to room temperature, filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent 5:95 to 2:3 EtOAc/hexanes) afforded ethyl(3-bromomethylphenyl)acetate as an off-white solid (0.89 g, 21%): 1H NMR (300 MHz, CDCl₃) δ 7.32-7.21 (m, 4H), 4.48 (s, 2H), 4.16 (q, J=6 Hz, 2H), 3.63, (s, 2H), 1.27 (t, J=6 Hz, 3H).

Step 2. Preparation of Ethyl {3-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]phenyl}acetate.

Ethyl {3-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]phenyl}-acetate was prepared by a procedure similar to the one described for EXAMPLE 74 (0.27 g, 69%): mp 95-98° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.65-7.55 (m, 1H), 7.40-7.20 (m, 5H), 7.00-6.80 (m, 2H), 6.09 (d, J=9 Hz, 1H), 5.21 (s, 2H), 5.16 (s, 2H), 4.14 (q, J=6 Hz, 2H), 3.60 (s, 2H), 1.25 (t, J=6 Hz, 3H). ESHRMS m/z 492.0655 (M+H C₂₃H₂₁BrF₂NO₄ requires 435.0617).

Example 128

Preparation of 2-{3-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]phenyl}acetamide

Example 128

The title compound was prepared by a procedure similar to the one described for EXAMPLE 102 (0.07 g, 28%): mp 164-167° C.; ¹H NMR (300 MHz, DMSO-d₆) δ 7.96 (d, J=9 Hz, 1H), 7.70-7.60 (m, 1H), 7.60 (br s, 1H), 7.50-7.10 (m, 6H), 6.89 (br s, 1H), 6.58 (d, J=9 Hz, 1H), 5.31 (s, 2H), 5.12 (s, 2H), 3.32 (s, 2H). ESHRMS m/z 463.0485 (M+H C₂₁H₁₈BrF₂N₂O₃ requires 463.0464).

Example 129

Preparation of 4-(2,4-Difluorobenzyloxy)-1-(3-fluorobenzyl)-3-methyl-1H-pyridin-2-one

Example 129

Step 1. Preparation of 4-(2,4-Difluorobenzyloxy)-1-(3-fluorobenzyl)-3-methyl-1H-pyridin-2-one.

To a solution of 3-bromo-4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one (EXAMPLE 107) (0.14 g, 0.32 mmol), K₂CO₃ (88 mg, 0.64 mmol) and Cs₂CO₃ (0.10 g, 0.32 mmol) in dioxane (2 mL) was added Pd(PPh₃)₄ (18 mg, 0.12 mmol), followed by trimethylboroxine (40 mg, 0.32 mmol). The reaction mixture was degassed, purged with argon, and heated at reflux for 4 h. The reaction mixture was cooled to room temperature, and partitioned between water and EtOAc. The organic solution was washed with brine, dried (Na₂SO₄), filtered and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent methylene chloride to 97:3 methylene chloride/MeOH) afforded 4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-3-methyl-1H-pyridin-2-one as a white solid (0.09 g, 79%): mp 127-129° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.50-7.40 (m, 1H), 7.35-7.25 (m, 1H), 7.17 (d, J=9 Hz, 1H), 7.06 (d, J=6 Hz, 1H), 7.00-6.80 (m, 4H), 6.12 (d, J=9 Hz, 1H), 5.12 (s, 4H), 2.07 (s, 3H). ESHRMS m/z 360.1180 (M+H C₂₀H₁₆F₃NO₂ requires 360.1206).

Example 130

Preparation of 4-(2,4-Difluorobenzyloxy)-1-(3-fluorobenzyl)-3-iodo-1H-pyridin-2-one

Example 130

Step 1. Preparation of 4-(2,4-Difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one.

To a mixture of 1-(3-fluorobenzyl)-4-hydroxy-1H-pyridin-2-one (from Step 1, EXAMPLE 110) (0.92 g, 4.2 mmol) and K₂CO₃ (1.15 g, 8.4 mmol) in acetone (62 mL) was added 2,4-difluorobenzyl bromide (1.3 g, 6.3 mmol), and the reaction mixture was heated at reflux for 3 h. The reaction mixture was cooled to room temperature, concentrated under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with water and then brine, dried (Na₂SO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent methylene chloride to 95:5 methylene chloride/methanol) provided 4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one as a white solid (1.21 g, 84%): ¹H NMR (300 MHz, CDCl₃) δ 7.45-7.20 (m, 2H), 7.14 (d, J=8 Hz, 1H), 7.05-6.75 (m, 5H), 6.05 (d, J=3 Hz, 1H), 5.95 (dd, J=5, 3 Hz, 1H), 5.08 (s, 2H), 5.00 (s, 2H).

Step 2. Preparation of 4-(2,4-Difluorobenzyloxy)-1-(3-fluorobenzyl)-3-iodo-1H-pyridin-2-one.

To a mixture of 4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-1H-pyridin-2-one (0.15 g, 0.43 mmol) and N-iodosuccinimide (0.10 g, 0.46 mmol) in CH₃CN (3 mL) was added dichloroacetic acid (13 mg, 0.10 mmol), and the reaction mixture was heated to 60° C. for 4 h. The reaction mixture was cooled to room temperature, concentrated under reduced pressure, and the residue was dissolved in methylene chloride. The organic solution was washed with a saturated solution of NaHCO₃ and then brine, dried (Na₂SO₄), filtered and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent 90:10 methylene chloride/hexanes to 99:1 methylene chloride/methanol) provided 4-(2,4-difluorobenzyloxy)-1-(3-fluorobenzyl)-3-iodo-1H-pyridin-2-one as a white solid (0.15 g, 77%): mp 164-167° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.65-7.55 (m, 1H), 7.35-7.26 (m, 2H) 7.15-6.80 (m, 5H), 6.05 (d, J=6 Hz, 1H), 5.22 (s, 2H), 5.16 (s, 2H). ESHRMS m/z 472.0033 (M+H C₁₉H₁₄F₃INO₂ requires 472.0018).

Example 131

Preparation of 4-(2,4-Difluorobenzyloxy)-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile

Example 131

Step 1. Preparation of 4-Methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile.

A solution of 2-(dimethylaminoethoxymethylene)malononitrile (1.97 g) in concentrated sulfuric acid (7.0 mL) was stirred at room temperature for 6.5 h. The reaction mixture was poured into water, and the precipitate was collected by filtration. ¹H NMR (300 MHz, DMSO-d₆) δ 12.14 (br s, 1H), 7.79 (d, J=9 Hz, 1H), 6.35 (d, J=9 Hz, 1H), 3.98 (s, 3H).

Step 2. Preparation of 1-(3-Fluorobenzyl)-4-methoxy-2-oxo-1,2-dihydro-pyridine-3-carbonitrile.

1-(3-Fluorobenzyl)-4-methoxy-2-oxo-1,2-dihydro-pyridine-3-carbonitrile was prepared by a procedure similar to the one described for EXAMPLE 74 (0.56 g, 93%): ¹H NMR (300 MHz, CDCl₃) δ 7.48 (d, J=9 Hz, 1H), 7.40-7.27 (m, 1H), 7.00-6.95 (m, 2H), 6.08 (d, J=9 Hz, 1H), 5.10 (s, 2H), 4.00 (s, 3H).

Step 3. Preparation of 1-(3-Fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carbonitrile.

To a solution of sodium hydride (92 mg of a 60% dispersion in mineral oil, 2.3 mmol) in DMF (7 mL) was added ethanethiol (0.14 g, 2.2 mmol), followed by a solution of 1-(3-fluorobenzyl)-4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile (0.23 g, 0.89 mmol) in DMF (2 mL), and the reaction mixture was heated to 100° C. The reaction mixture was cooled to room temperature, acidified with 3 N HCl, and washed with EtOAc. The organic solution was washed with brine, dried (Na₂SO₄), filtered and concentrated under reduced pressure to give 1-(3-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydro-pyridine-3-carbonitrile as an off-white solid (0.20 g, 91%): ¹H NMR (300 MHz, MeOD) δ 8.00 (s, 1H), 7.82 (d, J=8 Hz, 1H), 7.40-7.30 (m, 1H), 7.15-7.00 (m, 2H), 6.13 (d, J=8 Hz, 1H), 5.11 (s, 2H).

Step 4. Preparation of 4-(2,4-Difluorobenzyloxy)-1-(3-fluorobenzyl)-2-oxo-1,2-dihydro-pyridine-3-carbonitrile.

4-(2,4-Difluorobenzyloxy)-1-(3-fluorobenzyl)-2-oxo-1,2-dihydro-pyridine-3-carbonitrile was prepared by a procedure similar to the one described for EXAMPLE 107 (0.09 g, 30%): mp 187-190° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.60-7.45 (m, 2H), 7.40-7.30 (m, 1H), 7.10-6.50 (m, 5H), 6.13 (d, J=9 Hz, 1H), 5.27 (s, 2H), 5.10 (s, 2H).

Example 132

Preparation of 1-cyclohexyl-4-(2,4-difluorobenzyloxy)-3,6-dimethyl-1H-pyridin-2-one

Step 1. Preparation of methyl 1-cyclohexyl-4-hydroxy-2,5-dimethyl-6-oxo-1,6-dihydro-pyridine-3-carboxylate. To a solution of 3-cyclohexylaminobut-2-enoic acid methyl ester (1.12 g, 5.72 mmol) in bromobenzene (20 mL) was added 2-methylmalonic acid bis-(2,4,6-trichloro-phenyl)ester (2.71 g, 5.72 mmol) and the reaction mixture was heated at 170° C. for 3 h. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. Purification by flash column chromatography (silica, eluent methylene chloride to 94:6 methylene chloride/MeOH) and recrystallization from hot MeOH provided methyl 1-cyclohexyl-4-hydroxy-2,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylate as pale yellow crystals (0.34 g, 21%): ¹H NMR (500 MHz, DMSO-d₆) δ 9.82 (s, 1H), 4.00-3.90 (m, 1H), 3.76 (s, 3H), 2.75-2.60 (m, 2H), 2.31 (s, 3H), 1.81 (s, 3H), 1.80-1.70 (m, 2H), 1.65-1.50 (m, 3H), 1.40-1.20 (m, 2H), 1.15-1.05 (m, 1H).

Step 2. Preparation of 1-cyclohexyl-4-hydroxy-2,5-dimethyl-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid. A solution of methyl 1-cyclohexyl-4-hydroxy-2,5-dimethyl-6-oxo-1,6-dihydro-pyridine-3-carboxylate (0.35 g, 1.25 mmol) in 2 N NaOH (5 mL) was heated at reflux for 3.5 h. The reaction mixture was cooled room temperature, acidified to pH 1-2 with 1 N HCl, and washed with EtOAc. The organic solution was washed with brine, dried (MgSO₄), filtered and concentrated under reduced pressure to afford 1-cyclohexyl-4-hydroxy-2,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid as a white solid (0.31 g, 94%): 1H NMR (300 MHz, MeOD) δ 4.30-4.00 (br s, 1H), 2.76 (br s, 5H), 1.90 (s, 3H), 1.90-1.80 (m, 2H), 1.75-1.60 (m, 3H), 1.50-1.15 (m, 3H).

Step 3. Preparation of 1-cyclohexyl-4-hydroxy-3,6-dimethyl-1H-pyridin-2-one. A solution of 1-cyclohexyl-4-hydroxy-2,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (0.15 g, 0.57 mmol) in concentrated HCl (5 mL) was heated at reflux for 4 h. The reaction mixture was cooled to room temperature, diluted with water and washed with EtOAc. The organic solution was washed with brine, dried (MgSO₄), filtered and concentrated under reduced pressure to give 1-cyclohexyl-4-hydroxy-3,6-dimethyl-1H-pyridin-2-one as a white solid (0.2 g, 77%): ¹H NMR (300 MHz, DMSO-d₆) δ 9.81 (s, 1H), 5.73 (s, 1H), 3.95-3.75 (m, 1H), 2.80-2.55 (m, 2H), 2.25 (s, 3H), 1.85-1.40 (m, SH), 1.72 (s, 3H), 1.38-1.05 (m, 3H).

Step 4. Preparation of 1-cyclohexyl-4-(2,4-difluorobenzyloxy)-3,6-dimethyl-1H-pyridin-2-one. 1-Cyclohexyl-4-(2,4-difluorobenzyloxy)-3,6-dimethyl-1H-pyridin-2-one was prepared by a procedure similar to the one described for EXAMPLE 107 (0.05 g, 16%): mp 118-120° C.; ¹H NMR (300 MHz, CDCl₃) δ 7.48-7.41 (m, 1H), 6.95-6.81 (m, 2H), 5.87 (s, 1H), 5.07 (s, 2H), 4.05-3.85 (m, 1H), 3.00-2.80 (m, 2H), 2.35 (s, 3H), 1.98 (s, 3H), 1.95-1.80 (m, 2H), 1.70-1.55 (m, 3H), 1.40-1.20 (m, 3H).

Example 133

Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(1H-pyrazol-4-ylmethyl)-1H-pyridin-2-one

Step 1. Preparation of 4-methylpyrazole-1-carboxylic acid tert-butyl ester. To a solution of 4-methyl-1H-pyrazole (1 g, 12 mmol) and DMAP (0.15 g, 1.2 mmol) in CH₃CN (20 mL) was added di-tert-butyl dicarbonate (2.8 g, 13 mmol), and the reaction mixture was stirred for 1 h. The reaction mixture was concentrated under reduced pressure, and the residue dissolved in EtOAc. The organic solution was washed with 1 N HCl, water and then brine, dried (MgSO₄), filtered, and concentrated under reduced pressure to provide 4-methyl-pyrazole-1-carboxylic acid tert-butyl ester as a light yellow oil (2.2 g, 100%): ¹H NMR (300 MHz, CDCl₃) δ 7.83 (s, 1H), 7.53 (s, 1H), 2.09 (s, 3H), 1.64 (s, 9H).

Step 2. Preparation of 4-Bromomethylpyrazole-1-carboxylic acid tert-butyl ester. To a solution of 4-methylpyrazole-1-carboxylic acid tert-butyl ester (1.0 g, 5.5 mmol) in carbon tetrachloride (20 mL) was added N-bromosuccinimide (1.0 g, 5.6 mmol) and benzoyl peroxide (50 mg), and the reaction mixture was heated at reflux for 16 h. The reaction mixture was cooled to room temperature, filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:4 EtOAc/hexanes) provided 4-bromomethylpyrazole-1-carboxylic acid tert-butyl ester as a light yellow oil (0.42 g, 30%): ¹H NMR (300 MHz, CDCl₃) δ 8.10 (s, 1H), 7.74 (s, 1H), 4.39 (s, 2H), 1.65 (s, 9H).

Step 3. Preparation of 4-[3-chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]pyrazole-1-carboxylic acid tert-butyl ester. 4-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]pyrazole-1-carboxylic acid tert-butyl ester was prepared by a procedure similar to the one described for EXAMPLE 632: ¹H NMR (300 MHz, CDCl₃) δ 8.09 (s, 1H), 7.72 (s, 1H), 7.53 (app q, J=6 Hz, 1H), 6.97-6.82 (m, 2H), 6.00 (s, 1H), 5.19 (s, 2H), 5.13 (s, 2H), 2.43 (s, 3H), 1.63 (s, 9H).

Step 4. Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(1H-pyrazol-4-ylmethyl)-1H-pyridin-2-one. 4-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]pyrazole-1-carboxylic acid tert-butyl ester (0.16 g, 0.34 mmol) was heated to 140° C. for 16 h. The reaction mixture was cooled to room temperature. ¹H NMR (300 MHz, CDCl₃) δ 8.33 (s, 2H), 7.68 (d, J=6 Hz, 1H), 7.52 (app q, J=6 Hz, 1H), 6.93-6.83 (m, 2H), 6.47 68 (d, J=9 Hz, 1H), 5.19 (s, 2H), 5.24 (s, 2H), 5.20 (s, 2H).

Example 134

Preparation of 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

3-Bromo-4-[benzyloxy]-6-methylpyridin-2(1H)-one (1.0 g, 3.6 mmol) was dissolved in N,N-dimethylformamide (5 mL). α-Bromo-p-tolunitrile (0.85 g, 4.3 mmol) was added followed by K₂CO₃ (0.59 g, 4.3 mmol). The resulting mixture was heated to 80° C. for 16 h. The reaction was concentrated to an oil that was partitioned between water and ethyl acetate and extracted with ethyl acetate (3×100 ml). The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil, and purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid (0.65 g, 46%). ¹H NMR (400 MHz, CDCl₃) δ 7.62 (d, J=8.4 Hz, 2H), 7.41-7.31 (m, 7H), 7.23 (d, J=7.6 Hz, 1H), 6.11 (d, J=8.0 Hz, 1H), 5.24 (s, 2H), 5.18 (s, 2H). ES HRMS m/z 395.0404 (M+H C₂₀H₁₅BrN₂O₂ requires 395.0390).

Example 135

Preparation of 3-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

The title compound was prepared by a procedure essentially as described in example 134. ¹H NMR (400 MHz, CDCl₃) δ 7.62-7.54 (m, 3H), 7.45 (d, J=7.6 Hz, 1H), 7.43-7.31 (m, SH), 7.26 (d, J=1.6 Hz, 1H), 6.12 (d, J=1.6 Hz, 1H), 5.24 (s, 2H), 5.15 (s, 2H). ES HRMS m/z 395.0420 (M+H C₂₀H₁₅BrN₂O₂ requires 395.0390).

Example 136

Preparation of 2-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

The title compound was prepared by a procedure essentially as described in example 134. ¹H NMR (400 MHz, CDCl₃) δ 7.74 (d, J=8.4 Hz, 1H); 7.63 (dd, J=1.2, 8.0 Hz, 1H), 7.57 (dt, J=1.2, 8.4 Hz, 1H), 7.55 (d, J=8.0 Hz, 1H); 7.43-7.30 (m, 6H), 6.13 (d, J=8.0 Hz, 1H,), 5.33 (s, 2H), 5.23 (s, 2H). ES HRMS m/z 395.0398 (M+H C₂₀H₁₅BrN₂O₂ requires 395.0390).

Example 137

Preparation of 1-[4-(aminomethyl)benzyl]-4-(benzyloxy)-3-bromopyridin-2(1H)-one

Preparation of 1-[4-(aminomethyl)benzyl]-4-(benzyloxy)-3-bromopyridin-2(1H)-one. Example 134 (100 mg, 0.25 mmol) was dissolved in tetrahydrofuran (2 mL) under N₂. Borane dimethylsulfide complex (0.25 mL, 0.5 mmol, 2M in tetrahydrofuran) was added. The reaction was then heated to 70° C. and shaken overnight. The mixture was cooled and all the solvent was distilled under vacuum. The resulting residue was partitioned between ethyl acetate and 0.2 N NaOH, and extracted with ethyl acetate (3×10 mL). The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil, and triturated with dichloromethane and hexane to give an off-white solid. (80 mg, 80%). ¹H NMR (400 MHz, d₆DMSO) δ 7.90 (d, J=7.6 Hz, 1H); 7.43-7.21 (m, 9H), 6.70 (d, J=7.6 Hz, 1H), 5.29 (s, 2H), 5.08 (s, 2H), 3.71 (s, 2H). ES HRMS m/z 399.0721 (M+H C₂₀H₁₉BrN₂O₂ requires 399.0703).

Example 138

Preparation of 1-[3-(aminomethyl)benzyl]-4-(benzyloxy)-3-bromopyridin-2(1H)-one

The title compound was prepared by a procedure essentially as described in Example 137 using the title compound of Example 135 as starting material. ¹H NMR (400 MHz, d₆DMSO) δ 7.90 (d, J=7.6 Hz, 1H), 7.44-7.22 (m, 9H), 6.50 (d, J=7.6 Hz, 1H), 5.30 (s, 2H), 5.12 (s, 2<H), 3.88 (s, 2H). ES HRMS m/z 399.0730 (M+H C₂₀H₁₉BrN₂O₂ requires 399.0703).

Example 139

Preparation of 1-[2-(aminomethyl)benzyl]-4-(benzyloxy)-3-bromopyridin-2(1H)-one

The title compound was prepared by a procedure essentially as described in Example 137 using the title compound of Example 136 as starting material. ¹H NMR (400 MHz, d₆DMSO) δ 7.88 (d, J=8.0 Hz, 1H); 7.45-7.34 (m, 5H), 7.26-7.21 (m, 3H); 6.85 (d, J=7.2 Hz, 1H), 6.53 (d, J=7.6 Hz, 1H), 5.32 (s, 2H), 5.12 (s, 2H), 3.90 (s, 2H). ES HRMS m/z 399.0699 (M+H C₂₀H₁₉BrN₂O₂ requires 399.0703).

Example 140

Preparation of 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzamide

Preparation of 4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzamide. Example 134 (100 mg, 0.25 mmol) was added to a suspension of potassium fluoride (40% on alumina) in t-butyl alcohol, heated to 85° C., and stirred for 20 h. The alumina was removed by filtration and washed with dichloromethane and water. The resulting filtrate was separated and the aqueous layer was extracted with dichloromethane (2×20 mL). The organic extracts were combined, dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil. Trituration with dichloromethane and hexane gave a solid (11.5 mg, 11%). ¹H NMR (400 MHz, d₆DMSO) δ 7.94 (d, J=8.0 Hz, 1H), 7.80 (d, J=8.4 Hz, 2H); 7.43-7.29 (m, 7H), 6.51 (d, J=7.6 Hz, 1H), 5.31 (s, 2H), 5.16 (s, 2H). ES HRMS m/z 413.0541 (M+H C₂₀H₁₇BrN₂O₃ requires 413.0495).

Example 141

Preparation of 3-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzamide

The title compound was prepared by a procedure essentially as described in Example 140 using the title compound of Example 135 as starting material. ¹H NMR (400 MHz, d₆DMSO) δ 7.95 (d, J=7.6 Hz, 2H), 7.76 (m, 2H); 7.43-7.26 (m, 8H), 6.51 (d, J=7.6 Hz, 1H), 5.31 (s, 2H), 5.15 (s, 2H). ESHRMS m/z 413.0497 (M+H C₂₀H₁₇BrN₂O₃ requires 413.0495).

Example 142

Preparation of 2-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzamide

The title compound was prepared by a procedure essentially as described in Example 140 using the title compound of Example 136 as starting material. ¹H NMR (400 MHz, d₆DMSO) δ 7.78 (d, J=7.6 Hz, 1H), 7.54 (dd, J=1.6, 7.6 Hz, 1H); 7.45 (d, J=7.6 Hz, 2H); 7.44-7.32 (m, 5H), 7.15 (d, J=7.6 Hz, 1H), 6.49 (d, J=7.6 Hz, 1H), 5.39 (s, 2H), 5.30 (s, 2H). ES HRMS m/z 4413.0506 (M+H C₂₀H₁₇BrN₂O₃ requires 413.0495).

Example 143

Preparation of methyl-3-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzoate

Product from Example 135 (100 mg, 0.25 mmol) was suspended in methanol and cooled to 0° C. HCl (g) was bubbled through the mixture until saturated (˜30 minutes). The reaction was warmed to ambient temperature and stirred for 4 hours. HCl and methanol were removed in vacuo, yielding an oil, that was purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid (3 mg, 3%). ¹H NMR (400 MHz, CD₃OD) δ 7.98 (app d, J=8.0 Hz, 2H), 7.77 (app d, J=8.0 Hz, 1H); 7.55 (app d, J=8.0 Hz, 2H); 7.41-7.35 (m, 5H), 6.52 (d, J=7.6 Hz, 1H), 5.31 (s, 2H), 5.27 (s, 2H); 3.88, (s, 3H). API-ES MS m/z 429.0 (M+H C₂₁H₁₈BrNO₄ requires 428.0492).

Example 144

Preparation of methyl-4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}benzoate

The title compound was prepared by a procedure essentially as described in Example 143 using the title compound of Example 134 as starting material. ¹H NMR (400 MHz, CD₃OD) δ 7.94 (app d, J=8.4 Hz, 2H), 7.76 (app d, J=7.6 Hz, 1H); 7.46 (app d, J=8.0 Hz, 2H); 7.39-7.35 (m, 5H), 6.51 (d, J=7.6 Hz, 1H), 5.31 (s, 2H), 5.26 (s, 2H); 3.88, (s, 3H). ES HRMS m/z 428.0492 (M+H C₂₁H₁₈BrNO₄ requires 428.0492).

Example 145

Preparation of 4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzonitrile

3-bromo-4-[(benzyloxy]-6-methylpyridin-2(1H)-one (100 mg, 0.36 mmol) was suspended in dimethylsulfoxide (5 mL), cesium carbonate (375 mg, 1.15 mmol) was added and the reaction was shaken for 5 minutes. 4-Fluorobenzonitrile (52 mg, 0.43 mmol was then added, the reaction was heated to 80° C., and stirred. Reaction was monitored by LC/MS, and after 4 h was heated to 100° C. and stirred for 16 hours. Reaction mixture was partitioned between water and ethyl acetate and extracted with ethyl acetate (5×50 mL). The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil, and purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid (40 mg, 29%). ¹H NMR (400 MHz, CDCl₃) δ 7.77 (d, J=8.4 Hz, 2H), 7.52 (d, J=8.8 Hz, 2H), 7.44-7.42 (m, 4H), 7.28 (d, J=7.6 Hz, 1H), 7.26 (s, 1H), 6.24 (d, J=7.6 Hz, 1H); 5.31, (s, 2H). ES HRMS m/z 381.0230 (M+H Cl₉H₃BrN₂O₂ requires 381.0233).

Example 146

Preparation of 2-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzonitrile

3-bromo-4-[(benzyloxy]-6-methylpyridin-2(1H)-one (100 mg, 0.36 mmol) was suspended in dimethylsulfoxide (5 mL), cesium carbonate (375 mg, 1.15 mmol) was added and the reaction was shaken for 5 minutes. 4-Fluorobenzonitrile (52 mg, 0.43 mmol) was then added and the reaction was heated to 80° C. with stirring. Reaction was monitored by LC/MS, and after 4 h was heated to 100° C. and stirred for 16 hours. The reaction mixture was partitioned between water and ethyl acetate and extracted with ethyl acetate (5×50 mL). The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil, and purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid (18 mg, 13%). ¹H NMR (400 MHz, CDCl₃) δ 7.81 (dd, J=1.2, 8.4 Hz, 1H), 7.73 (dt, J=1.2, 8.0 Hz, 1H), 7.57 (dt, J=0.8, 8.0 Hz, 1H), 7.50-7.36 (m, 6H), 7.27 (d, J=8.0 Hz, 1H), 6.28 (d, J=8.0 Hz, 1H); 5.31 (s, 2H). ES HRMS m/z 381.0249 (M+H C₁₉H₁₃BrN₂O₂ requires 381.0233).

Example 147

Preparation of (4-{[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]methyl}phenyl)acetic Acid

3-bromo-4-[(benzyl)oxy]-6-methylpyridin-2(1H)-one (0.5 g, 1.78 mmol) was dissolved in N,N-dimethylformamide (5 mL). 4-(Bromomethyl)phenylacetic acid (0.5 g, 2.14 mmol) was added followed by K₂CO₃ (0.3 g, 2.14 mmol). The reaction was heated to 80° C. and shaken for 16 hours, then heated to 100° C. and shaken for 16 hours more. The reaction mixture was partitioned between water and ethyl acetate and extracted with ethyl acetate (2×50 mL). The aqueous layer was acidified (pH 2) with 1N HCl and extracted with ethyl acetate (3×50 ml). The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil, and purified by chromatography (silica gel, hexane/ethyl acetate) followed by reversed phase chromatography (C₁₈, 0.1% aqueous trifluoroacetic acid/acetonitrile) to yield a white solid (25 mg, 3%). ¹H NMR (400 MHz, CDCl₃) δ 7.40-7.38 (m, 3H), 7.25-7.20 (m, 7H), 6.05 (d, J=8.0 Hz, 1H), 5.21 (s, 2H); 5.13, (s, 2H); 3.62, (s, 2H). ES HRMS m/z 428.0510 (M+H C₂₁H₁₈BrNO₄ requires 428.0492).

Example 148

Preparation of {4-[(4-(benzyloxy)-3-bromo-2-{[4-(carboxymethyl)benzyl]oxy}-1lambda⁵-pyridin-1-yl)methyl]phenyl}acetic Acid

The desired product was isolated by reversed phase chromatography (C₁₈, 0.1% aqueous trifluoroacetic acid/acetonitrile) using the preparation of Example 147 yielding a white solid (53 mg, 5%). ¹H NMR (400 MHz, CDCl₃) δ 7.40-7.38 (m, 3H), 7.27-7.24 (m, 6H), 7.20 (d, J=7.6 Hz, 1H), 7.14 (d, J=8.0 Hz, 2H), 7.08 (d, J=8.4 Hz, 1H), 6.06 (d, J=7.6 Hz, 1H), 5.21 (s, 2H); 5.11 (s, 2H); 5.11 (s, 2H); 3.63 (s, 2H); 3.58 (s, 2H). ES HRMS m/z 576.1009(M+H C₃₀H₂₈BrNO₆ requires 576.1016).

Example 149

Preparation of 2-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

3-bromo-4-(2,4-difluorophenoxy)-6-methylpyridin-2(1H)-one (50 mg, 0.15 mmol) was dissolved in tetrahydrofuran (2 mL). α-Bromo-o-tolunitrile (44 mg, 0.23 mmol) was added followed by sodium hydride (7.2 mg, 0.18 mmol, 60% in mineral oil) and sodium iodide (56 mg, 0.38 mmol). The reaction was heated to 50° C. and stirred for 16 hours. The reaction was filtered through Celite® and the filtrate was concentrated to an oil that was partitioned between water and ethyl acetate and extracted with ethyl acetate (4×10 mL). The organic extracts were combined, washed with brine, dried over MgSO₄, and filtered. The filtrate was concentrated to an oil, and purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid (25 mg, 37%). ¹H NMR (400 MHz, CDCl₃) δ 7.68 (dd, J=8.0, 1.2 Hz, 1H); 7.58 (app q, J=8.8 Hz, 1H); 7.52 (dt, J=8.0 & 1.2 Hz, 1H), 7.38 (t, J=7.6 Hz, 1H); 7.08 (d, J=8.8 Hz, 1H), 7.00-6.93 (m, 1H); 6.89-6.84 (m, 1H); 6.05 (s, 1H), 5.57 (s, 2H), 5.22 (s, 2H); 2.28, (s, 3H). ES HRMS m/z 445.0335 (M+H C₂₁H₁₅BrF₂N₂O₂ requires 445.0358).

Example 150

Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

The title compound was prepared by a procedure essentially as described in Example 149 using 3-bromo-4-(2,4-difluorophenoxy)-6-methylpyridin-2(1H)-one (1 g, 3.0 mmol) as starting material. ¹H NMR (CDCl₃, 400 MHz) δ 7.61-7.55 (m, 2H); 7.45-7.41 (m, 3H); 6.98-6.94 (m, 1H); 6.89-6.84 (m, 1H); 6.03 (s, 1H), 5.36 (s, 2H), 5.22 (s, 2H); 2.30, (s, 3H). ES HRMS m/z 445.0349 (M+H C₂₁H₁₅BrF₂N₂O₂ requires 445.0358).

Example 151

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

The title compound was prepared by a procedure essentially as described in Example 149 using 3-bromo-4-(2,4-difluorophenoxy)-6-methylpyridin-2(1H)-one (1 g, 3.0 mmol) as starting material. ¹H NMR (400 MHz, CDCl₃) δ 7.61 (d, J=8.4 Hz, 2H); 7.62-7.56 (m, 1H); 7.27 (d, J=8.8 Hz, 2H); 6.95 (app t, J=8.4 Hz, 1H), 6.88-6.83 (m, 1H); 6.03 (s, 1H), 5.39 (s, 2H), 5.21 (s, 2H); 2.28 (s, 3H). ES HRMS m/z 445.0359 (M+H C₂₁H₁₅BrF₂N₂O₂ requires 445.0358).

Example 152

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide

Product from Example 151 (50 mg, 0.11 mmol) was added to a suspension or potassium fluoride (40% on alumina) in t-butyl alcohol. The reaction was heated to 90° C. and stirred for 20 hours. Alumina was removed by filtration and washed with dichloromethane and water. The resulting filtrate was separated and the aqueous layer was extracted with dichloromethane (2×20 mL). The organic extracts were combined, dried over Na₂SO₄ and filtered. The filtrate was concentrated to an oil which was purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid, yielding the product (13 mg, 25%). ¹H NMR (400 MHz, CDCl₃) δ 7.75 (app d, J=8.4 Hz, 2H), 7.58 (app q, J=8.4 Hz, 1H); 7.24 (d, J=8.4 Hz, 2H); 6.98-6.94 (m, 1H), 6.89-6.83 (m, 1H) 6.01 (s, 1H); 5.40 (s, 2H), 5.21 (s, 2H); 2.28 (s, 3H). ES HRMS m/z 463.0486 (M+H C₂₁H₁₇BrF₂N₂O₃ requires 463.0463).

Example 153

Preparation of Methyl 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoate

Product from Example 151 (50 mg, 0.11 mmol) was suspended in methanol and cooled to 0° C. HCl (g) was bubbled through the mixture until saturated (30 minutes). Reaction was sealed, warmed to ambient temperature, and stirred for 2 hours. HCl and methanol were removed in vacuo, yielding an oil, that was purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid (19 mg, 36%). ¹H NMR (400 MHz, CDCl₃) δ 7.97 (app d, J=8.4 Hz, 2H), 7.58 (app q, J=8.0 Hz, 1H); 7.22 (d, J=8.4 Hz, 2H); 6.95 (app dt, J=1.5, 9.6 Hz, 1H), 6.89-6.83 (m, 1H), 6.00 (s, 1H); 5.41 (s, 2H), 5.21 (s, 2H); 3.90, (s, 3H); 2.27 (s, 3H). ES HRMS m/z 478.0461 (M+H C₂₂H₁₈BrNO₄ requires 478.0460).

Example 154

Preparation of Methyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoate

The title compound was prepared by a procedure essentially as described in Example 149 using the title compound of Example 150 as starting material. ¹H NMR (400 MHz, CDCl₃) δ 7.95-7.92 (m, 1H); 7.84 (bs, 1H); 7.58 (app q, J=8.0 Hz, 1H); 7.39-7.37 (m, 2H); 6.95 (app dt, J=1.6, 8.4 Hz, 1H), 6.88-6.83 (m, 1H), 6.00 (s, 1H); 5.40 (s, 2H), 5.21 (s, 2H); 3.90, (s, 3H); 2.30 (s, 3H). ES HRMS m/z 478.0449 (M+H C₂₂H₁₈BrNO₄ requires 478.0460).

Example 155

Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide

The title compound was prepared by a procedure essentially as described in Example 152 using the title compound of Example 150 as starting material. ¹H NMR (400 MHz, CDCl₃) δ 7.68-7.66 (m, 2H), 7.57 (app q, J=8.4 Hz, 1H); 7.42-7.34 (m, 2H); 6.98-6.92 (m, 1H), 6.89-6.83 (m, 1H) 6.01 (s, 1H); 5.39 (s, 2H), 5.21 (s, 2H); 2.28 (s, 3H). ES HRMS m/z 463.0461 (M+H C₂₁H₁₇BrF₂N₂O₃ requires 463.0463).

Example 156

Preparation of 2-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide

The title compound was prepared by a procedure essentially as described in Example 152 using the title compound of Example 149 as starting material. ¹H NMR (400 MHz, CDCl₃) δ 7.68-7.66 (m, 2H), 7.57 (app q, J=8.4 Hz, 1H); 7.42-7.34 (m, 2H); 6.98-6.92 (m, 1H), 6.89-6.83 (m, 1H) 6.01 (s, 1H); 5.39 (s, 2H), 5.21 (s, 2H); 2.28 (s, 3H). ES HRMS m/z 463.0461 (M+H C₂₁H₁₇BrF₂N₂O₃ requires 463.0463). ¹H NMR (400 MHz, CDCl₃) δ 7.56-7.55 (m, 2H); 7.32-7.25 (m, 2H); 7.00-6.94 (m, 1H), 6.88-6.84 (m, 1H); 6.81-6.79 (m, 1H) 6.11 (s, 1H); 5.51 (s, 2H), 5.24 (s, 2H); 2.43 (s, 3H). ESHRMS m/z 463.0467 (M+H C₂₁H₁₇BrF₂N₂O₃ requires 463.0463).

Example 157

Preparation of 1-[2-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Product from Example 149 (50 mg, 0.11 mmol) was dissolved in tetrahydrofuran (2 mL) under N₂. Borane-methyl sulfide complex (0.11 mL, 0.22 mmol, 2M in tetrahydrofuran) was added. The reaction was then heated to 70° C. and shaken overnight. After cooling to ambient temperature, all the solvent was distilled under vacuum. The resulting residue was partitioned between ethyl acetate and 0.2 N NaOH, and extracted with ethyl acetate (3×20 mL). The organic extracts were combined, washed with brine, and dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil, and purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid, to give product (19 mg, 39%). ¹H NMR (400 MHz, CDCl₃) δ 7.56-7.55 (m, 2H); 7.32-7.25 (m, 2H); 7.00-6.94 (m, 1H), 6.88-6.84 (m, 1H); 6.81-6.79 (m, 1H); 6.11 (s, 1H); 5.44 (s, 2H), 5.17 (s, 2H); 4.59 (s, 2H); 2.18 (s, 3H). ESHRMS m/z 449.0692 (M+H C₂₁H₁₉BrF₂N₂O₂ requires 449.0671).

Example 158

Preparation of 3-bromo-1-[3-(bromomethyl)benzyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (2 g, 6.06 mmol) was suspended in 1,4-dioxane (250 mL). α,α′-Dibromo-m-xylene (8 g, 30.3 mmol) was added followed by sodium hydride (0.3 g, 7.5 mmol, 60% in mineral oil). The reaction was heated to 60° C. and stirred for 16 hours. The reaction was filtered through Celite® and the filtrate was concentrated to an oil that was partitioned between water and dichloromethane and extracted with dichloromethane (4×250 mL). The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil, and purified by chromatography (silica gel, hexane/ethyl acetate) to yield a white solid (1.2 g, 38%). ¹H NMR (400 MHz, CDCl₃) δ 7.57 (app q, J=7.6 Hz, 1H); 7.28-7.25 (m, 2H); 7.17 (s, 1H); 7.08 (m, 1H); 6.94 (app dt, J=1.2, 9.6 Hz, 1H), 6.87-6.82 (m, 1H); 5.99 (s, 1H), 5.34 (s, 2H), 5.20 (s, 2H); 4.43 (s, 2H); 2.29 (s, 3H). ES HRMS m/z 511.9672 (M+H C₂₁H₁₇Br₂F₂NO₂ requires 511.9667).

Example 159

Preparation of 3-bromo-1-[4-(bromomethyl)benzyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

The title compound was prepared by a procedure essentially as described in Example 158. ¹H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=7.6 Hz, 1H); 7.32 (d, J=8.0 Hz, 2H); 7.14 (d, J=8.0 Hz, 2H); 6.94 (app t, J=8.4 Hz, 1H), 6.87-6.82 (m, 1H); 5.98 (s, 1H), 5.33 (s, 2H), 5.19 (s, 2H); 4.44 (s, 2H); 2.29 (s, 3H). ES HRMS m/z 511.9683 (M+H C₂₁H₁₇Br₂F₂NO₂ requires 511.9667).

Example 160

Preparation of 1-[4-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Product from Example 159 (200 mg, 0.39 mmol) was suspended in methanol (3 mL) and cooled to −78° C. Ammonia (g) was bubbled through the mixture for 30 minutes. The reaction vessel was sealed, allowed to reach ambient temperature, and stirred for 4 hours. The solvent and ammonia were removed from the reaction in vacuo with stirring and the resulting oil was triturated with ether to yield a solid (174 mg, 99%). ¹H NMR (400 MHz, CD₃OD) δ 7.61 (q, J=7.6 Hz, 1H); 7.40 (d, J=8.0 Hz, 2H); 7.20 (d, J=8.0 Hz, 2H); 7.03 (app t, J=8.8 Hz, 2H), 6.51 (s, 1H), 5.43 (s, 2H), 5.29 (s, 2H); 4.07 (s, 2H); 2.36 (s, 3H). ES HRMS m/z 449.0673 (C₂₁H₁₉BrF₂N₂O₂ requires 449.0671).

Examples 161-168

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 161-168 are prepared essentially according to the procedures set forth above for Examples 158-160 or by using the compound of Example 158:

Example			M + H	ESHRMS
No.	R	MF	Requires	m/z
Ex. 161	—NH2	C21H19BrF2N2O2	449.0671	449.0694
Ex. 162	morpholin-4-yl	C25H25BrF2N2O3	519.1089	519.1132
Ex. 163	dimethylamino	C23H23BrF2N2O2	477.0984	477.0991
Ex. 164	isopropylamino	C24H25BrF2N2O2	491.1140	491.1121
Ex. 165	piperidin-1-yl	C26H27BrF2N2O2	517.1297	517.1341
Ex. 166	(2-hydroxy-	C23H23BrF2N2O3	493.0933	493.0961
	ethyl)amino
Ex. 167	bis(2-hydroxy-	C25H27BrF2N2O4	537.1195	537.1171
	ethyl)amino
Ex. 168	piperazin-1-yl	C25H26BrF2N3O2	518.1249	518.1280

NMR characterization of compounds of Examples 161-168

Ex. No. NMR Data
Ex. 161 1H NMR (400MHz, CD3OD) δ 7.61(q, J=7.6Hz, 1H); 7.42-7.35(m, 2H), 7.24-7.20(m,
        2H), 7.03(app t, J=8.4Hz, 2H), 6.51(s, 1H), 5.43(s, 2H), 5.29(s, 2H); 4.07(s, 2H); 2.04
        (s, 3H)
Ex. 162 1H NMR (400MHz, CD3OD) δ 7.58(app q, J=7.6Hz, 1H); 7.26-7.22(m, 2H), 7.15(s,
        2H), 7.01(app d, J=6.4Hz, 2H), 6.95(app dt, J=1.2, 8.0Hz, 1H); 6.88-6.82(m, 1H); 5.98
        (s, 1H), 5.35(s, 2H), 5.20(s, 2H); 3.69(t, J=8.4Hz, 4H); 3.46(s, 2H); 2.41(m, 4H); 2.29
        (s, 3H)
Ex. 163 1H NMR (400MHz, CD3OD) δ 7.61(app q, J=7.6Hz, 1H); 7.25-7.14(m, 3H); 7.01-6.92
        (m, 2H); 6.85(m, 1H); 5.97(s, 1H), 5.36(s, 2H), 5.20(s, 2H); 3.38(s, 2H); 2.28(s, 3H);
        2.21(s, 6H)
Ex. 164 1H NMR (400MHz, CDCl3) δ 7.61(app q, J=8.0Hz, 1H); 7.25-7.22(m, 2H); 7.14(s, 1H),
        6.99(app d, 6.8Hz, 1H), 6.94(app dt, J=2.0, 8.0Hz, 1H), 6.88-6.80(m, 1H); 5.97(s, 1H),
        5.34(s, 2H), 5.19(s, 2H); 3.73(s, 2H); 2.28(s, 3H); 2.82(app heptet, J=6.0Hz, 1H), 1.07
        (d, J=6.0Hz, 6H)
Ex. 165 1H NMR (400MHz, CD3OD) δ 7.61(app q, J=8.0Hz, 1H); 7.27(app t, J=8.0Hz, 1H);
        7.20(app d, J=7.6Hz, 1H); 7.08(bs, 1H); 7.01(app t, J=8.0Hz, 2H); 6.48(s, 1H), 5.41
        (s, 2H), 5.28(s, 2H); 3.44(s, 2H); 2.35(s, 3H); 2.40-2.30(m, 4H); 1.57-1.53(m, 4H); 1.48-
        1.38(m, 2H)
Ex. 166 1H NMR (400MHz, CDCl3) δ 7.51(app q, J=8.0Hz, 1H); 7.22-7.14(m, 3H); 7.09(bs,
        1H); 6.98(app d, J=7.2Hz, 1H); 6.89(app dt, J=1.6, 8.0Hz, 1H); 6.81-6.76(m, 1H); 5.92
        (s, 1H), 5.28(s, 2H), 5.14(s, 2H); 3.73(s, 2H); 3.59(app t, J=4.8Hz, 2H); 2.73(app t, J=4.8Hz,
        2H); 2.24(s, 3H)
Ex. 167 1H NMR (400MHz, CD3OD) δ 7.61(app q, J=8.0Hz, 1H); 7.46(app d, J=8.8Hz,
        2H); 7.31(bs, 1H); 7.27(app t, J=8.0Hz, 1H); 7.03(app t, J=8.8Hz,
        2H); 6.54(s, 1H), 5.44(s, 2H), 5.30(s, 2H); 4.47(s, 2H); 3.90-3.84(m,
        4H); 3.40-3.25(m, 4H); 2.40(s, 3H)
Ex. 168 1H NMR (400MHz, CD3OD) δ 7.62(app q, J=8.0Hz, 1H); 7.53-7.46(m, 2H); 7.36(bs,
        1H); 7.30(app d, J=7.6Hz, 1H); 7.05-7.01(m, 2H); 6.55(s, 1H), 5.44(s, 2H), 5.30(s, 2H);
        4.47(s, 2H); 3.58-3.53(m, 8H); 2.42(s, 3H)

Example 169

Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid

Product from Example 154 (150 mg, 0.31 mmol) was dissolved in tetrahydrofuran (5 mL). Potassium trimethylsilanolate (80 mg, 0.62 mmol) was added and the reaction was stirred at ambient temperature for 4 hours. The reaction mixture was concentrated to an oil that was partitioned between water and ethyl acetate and extracted with ethyl acetate. The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The filtrate was concentrated to an oil and purified by reversed phase chromatography (C₁₈, 0.1% aqueous trifluoroacetic acid/acetonitrile) to yield the product (64 mg, 44%) ¹H NMR (400 MHz, CD₃OD) δ 7.92 (app d, J=8.0 Hz, 1H); 7.78 (s, 1H); 7.62 (app q, J=8.0 Hz, 1H); 7.44 (t, J=7.6 Hz, 1H); 7.36 (app d, J=8.0 Hz, 1H); 7.02 (app t, J=7.6 Hz, 2H); 6.51 (s, 1H), 5.48 (s, 2H), 5.30 (s, 2H); 2.37 (s, 3H). ES HRMS m/z 464.0328 (C₂₁H₁₆BrF₂NO₄ requires 464.0304).

Examples 170-174

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 170-174 are prepared using the compound of Example 159 or 161:

Example			M + H	ESHRMS
No.	R	MF	Requires	m/z
Ex. 170	—C(O)CH3	C23H21BrF2N2O3	491.0776	491.0772
Ex. 171	—C(O)OCH3	C23H21BrF2N2O4	507.0726	507.0731
Ex. 172	—SO2CH3	C22H21BrF2N2O4S	527.0446	527.0430
Ex. 173	—C(O)CH2OH	C23H21BrF2N2O4	507.0726	507.0712
Ex. 174	—C(O)NH2	C22H20BrF2N3O3	492.0729	492.0751

NMR characterization of compounds of Examples 170-174

Ex. No. NMR Data
Ex. 170 1H NMR (400MHz, CD3OD) δ 7.61(app q, J=8.0Hz, 1H); 7.28(app t, J=8.0, 1H), 7.18
        (app d, J=8.0Hz, 1H), 7.05-7.00(m, 4H); 6.49(s, 1H), 5.41(s, 2H), 5.29(s, 2H); 2.37(s,
        3H); 1 .94(s, 3H)
Ex. 171 1H NMR (400MHz, CDCl3) δ 7.57(app q, J=7.6Hz, 1H); 7.25(app t, J=8.0, 1H), 7.17
        (app d, J=8.0Hz, 1H), 7.06-7.02(m, 2H); 6.97-6.91(m, 1H); 6.87-6.82(m, 1H), 5.98(s,
        1H), 5.33(s, 2H), 5.19(s, 2H); 4.30(d, J=6.0Hz, 2H); 3.67(s, 3H); 2.28(s, 3H)
Ex. 172 1H NMR (400MHz, CD3CN) δ 7.58(app q, J=7.6Hz, 1H); 7.31(app t, J=8.0, 1H), 7.24
        (app d, J=8.0Hz, 1H), 7.11(s, 1H); 7.05-7.00(m, 3H); 6.32(s, 1H), 6.06(bs, 1H), 5.31(s,
        2H), 5.23(s, 2H); 4.17(d, J=6.4Hz, 2H); 2.78(s, 3H); 2.28(s, 3H)
Ex. 173 1H NMR (400MHz, CDCl3) δ 7.55(app q, J=8.0Hz, 1H); 7.23(app t, J=7.6, 1H), 7.15
        (app d, J=7.2Hz, 1H), 7.05-7.00(m, 3H); 6.94(app dt, J=1.2, 8.8Hz, 1H); 6.88-6.81(m,
        1H); 6.03(s, 1H), 5.27(s, 2H), 5.19(s, 2H); 4.39(d, J=6.4Hz, 2H); 4.05(s, 2H), 2.31(s,
        3H)
Ex. 174 1H NMR (400MHz, CD3OD) δ 7.62(app q, J=8.0Hz, 1H); 7.28(app t, J=8.0, 1H), 7.19
        (app d, J=8.0Hz, 1H), 7.05-6.96(m, 4H); 6.49(s, 1H), 5.41(s, 2H), 5.29(s, 2H); 4.25(s,
        2H); 2.35(s, 3H)

Examples 175-185

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 175-185 are prepared using the compounds of Examples 159 or 160:

Example			M + H	ESHRMS
No.	R	MF	Requires	m/z
Ex. 175	—CH2NHCH(CH3)2	C24H25BrF2N2O2	491.1140	491.1143
Ex. 176	morpholin-4-ylmethyl	C25H25BrF2N2O3	519.1089	519.1062
Ex. 177	—CH2N(CH3)2	C23H23BrF2N2O2	477.0984	477.0931
Ex. 178	piperidin-1-ylmethyl	C26H27BrF2N2O2	517.1297	517.1258
Ex. 179	[bis(2-	C25H27BrF2N2O4	537.1195	537.1181
	hydroxyethyl)amino]mehtyl
Ex. 180	—CH2NHCH2CH2OH	C23H23BrF2N2O3	493.0933	493.0907
Ex. 181	piperazin-1-ylmethyl	C25H26BrF2N3O2	518.1249	518.1213
Ex. 182	—CH2NHC(O)OCH3	C23H21BrF2N2O4	507.0726	507.0752
Ex. 183	—CH2NHC(O)CH3	C23H21BrF2N2O3	491.0776	491.0793
Ex. 184	—CH2NHSO2CH3	C22H21BrF2N2O4S	527.0446	527.0431
Ex. 185	—CH2NHC(O)NH2	C22H20BrF2N3O3	492.0729	492.0720

NMR characterization of compounds of Examples 175-185

Ex. No. NMR Data
Ex. 175 1H NMR (400MHz, CDCl3) δ 7.56(q, J=8.0Hz, 1H); 7.25(d, J=8.0Hz, 2H), 7.10(d, J=8.0Hz,
        2H), 6.94(app t, J=8.0Hz, 1H), 6.88-6.80(m, 1H); 5.97(s, 1H), 5.31(s, 2H), 5.19
        (s, 2H); 3.74(s, 2H); 2.82(app heptet, J=6.0Hz, 1H), 2.28(s, 3H); 1.09(d, J=6.4Hz, 6H)
Ex. 176 1H NMR (400MHz, CDCl3) δ 7.56(q, J=8.0Hz, 1H); 7.25(d, J=8.0Hz, 2H), 7.11(d, J=8.0Hz,
        2H), 6.94(app dt, J=2.0, 8.0Hz, 1H), 6.87-6.81(m, 1H); 5.97(s, 1H), 5.33(s, 2H),
        5.19(s, 2H); 3.67(app t, J=4.8Hz, 4H); 3.44(s, 2H); 2.44-2.38(m, 4H), 2.29(s, 3H)
Ex. 177 1H NMR (400MHz, CDCl3) δ 7.56(q, J=8.0Hz, 1H); 7.23(d, J=8.0Hz, 2H), 7.11(d, J=8.0Hz,
        2H), 6.93(app dt, J=2.0, 8.0Hz, 1H), 6.86-6.81(m, 1H); 5.96(s, 1H), 5.33(s, 2H),
        5.18(s, 2H); 3.38(s, 2H); 2.29(s, 3H); 2.20(s, 6H)
Ex. 178 1H NMR (400MHz, CDCl3) δ 7.56(q, J=8.0Hz, 1H); 7.24-7.20(m, 2H), 7.10-7.07(m,
        2H), 6.96-6.90(m, 1H), 6.86-6.81(m, 1H); 5.96(s, 1H), 5.32(s, 2H), 5.18(s, 2H); 3.34(s,
        2H); 2.31(s, 3H); 2.31-2.28(m, 4H); 1.53-1.51(m, 4H); 1.39(m, 2H)
Ex. 179 1H NMR (400MHz, CDCl3) δ 7.57(q, J=8.0Hz, 1H); 7.25(d, J=8.0Hz, 2H); 7.12(d, J=8.0Hz,
        2H); 6.94(dt, J=8.8Hz, 2H); 6.87-6.82(m, 1H), 5.98(s, 1H), 5.33(s, 2H), 5.19(s,
        2H); 3.68(s, 2H); 3.61(t, J=5.2Hz, 4H); 2.70(t, J=5.2Hz, 4H); 2.29(s, 3H)
Ex. 180 1H NMR (400MHz, CDCl3) δ 7.57(q, J=8.0Hz, 1H); 7.25(d, J=8.0Hz, 2H); 7.12(d, J=8.0Hz,
        2H); 6.94(app dt, J=8.8Hz, 2H); 6.87-6.82(m, 1H), 5.98(s, 1H), 5.33(s, 2H), 5.19
        (s, 2H); 3.68(s, 2H); 3.61(t, J=5.2Hz, 4H); 2.70(t, J=5.2Hz, 4H); 2.29(s, 3H)
Ex. 181 1H NMR (400MHz, CDCl3) δ 7.61(q, J=8.0Hz, 1H); 7.52(d, J=8.0Hz, 2H); 7.25(d, J=8.0Hz,
        2H); 7.03(app t, J=8.0Hz, 2H); 6.53(s, 1H), 5.44(s, 2H), 5.30(s, 2H); 4.32(bs,
        2H); 3.55-3.35(m, 8H); 2.39(s, 3H)
Ex. 182 1H NMR (400MHz, CDCl3) δ 7.56(app q, J=8.0Hz, 1H); 7.20(d, J=8.0Hz, 1H), 7.13(d,
        J=8.0Hz, 2H), 6.94(app dt, J=1.2, 8.0Hz, 1H), 6.87-6.81(m, 2H); 5.97(s, 1H), 5.32(s,
        2H), 5.19(s, 2H); 4.31(d, J=6.0Hz, 2H); 3.68(s, 3H); 2.28(s, 3H)
Ex. 183 1H NMR (400MHz, CDCl3) δ 7.61(app q, J=8.0Hz, 1H); 7.23(d, J=8.0Hz, 2H), 7.08(d,
        J=8.0Hz, 2H), 7.04-6.99(m, 2H); 6.47(s, 1H), 5.39(s, 2H), 5.28(s, 2H); 4.30(s, 2H); 2.34
        (s, 3H); 1.95(s, 3H)
Ex. 184 1H NMR (400MHz, CD3OD) δ 7.62(app q, J=8.0Hz, 1H); 7.34(d, J=8.4Hz, 2H), 7.11
        (d, J=8.4Hz, 2H), 7.02(app t, J=8.8Hz, 2H), 6.48(s, 1H), 5.42(s, 2H), 5.28(s, 2H); 4.21
        (s, 2H); 2.82(s, 3H); 2.35(s, 3H)
Ex. 185 1H NMR (400MHz, d7DMF) δ 7.76(app q, J=8.0Hz, 1H); 7.28(d, J=8.0Hz, ), 7.14(d,
        J=8.0Hz, 2H), 7.34-7.26(m, 1H); 7.22-7.14(m, 1H); 6.62(s, 1H), 5.65(s, 2H), 5.39(s,
        2H), 5.37(s, 2H); 4.26(d, J=6.0Hz, 2H); 2.40(s, 3H)

Example 186

Preparation of 4-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoyl)piperazine-1-carboxamide

3-bromo-4-(2,4-difluorophenoxy)-6-methyl-1-[4-(piperazin-1-ylcarbonyl)benzyl]pyridin-2(1H)-one (300 mg, 0.54 mmol) was dissolved in N,N-dimethylacetamide (5 mL). Trimethylsilyl isocyanate (0.15 mL, 1.08 mmol) was added followed by N,N-diisopropylethylamine (0.23 mL, 1.3 mmol) and the reaction was stirred for 1 hour at ambient temperature. The reaction was then diluted with tetrahydrofuran (40 mL) and polyamine resin (1.3 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (1 g, 1.38 mmol/g) were added. The mixture was shaken for 6 hours, filtered, and the resulting filtrate was concentrated to a white solid (279 mg, 90%). ¹H NMR (400 MHz, CD₃OD) δ 7.61 (app q, J=8.0 Hz, 1H); 7.41 (d, J=8.0 Hz, 2H), 7.23 (d, J=8.0 Hz, 2H), 7.03 (app t, J=8.8 Hz, 2H); 6.51 (s, 1H), 5.46 (s, 2H), 5.30 (s, 2H), 3.75-3.35 (m, 8H); 2.37 (s, 3H). ES HRMS m/z 575.1104 (C₂₆H₂₅BrF₂N₄O₄ requires 575.1100).

Example 187

Preparation of N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-2-methoxyacetamide

Polymer bound carbodiimide resin (2.3 g, 1.18 meq/g, 2.7 mmol) was suspended in N,N-dimethylformamide. Methoxyacetic acid (120 mg, 1.33 mmol) was added, followed by 1-hydroxybenzotriazole (1M in N,N-dimethylformamide, 0.165 mL) and N,N-diisopropylethylamine (0.3 mL, 2.0 mmol). The reaction was shaken for 1 hour when EXAMPLE 160 (300 mg, 0.67 mmol) was added. The reaction was shaken for 16 hours and then diluted with tetrahydrofuran. Polyamine resin (1 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (2 g, 1.38 mmol/g) were added and the mixture was shaken for 72 hours, filtered and the resulting filtrate concentrated. Trituration with water followed by trituration with ether yielded a white solid (125 mg, 36%). ¹H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=8.0 Hz, 1H); 7.21 (d, J=8.0 Hz, 2H), 7.13 (d, J=8.0 Hz, 2H), 6.94 (app t, J=8.8 Hz, 1H), 6.88-6.81 (m, 1H); 5.97 (s, 1H), 5.33 (s, 2H), 5.19 (s, 2H); 4.43 (d, J=6.0 Hz, 2H); 3.92 (s, 2H); 3.39 (s, 3H); 2.29 (s, 3H). ES HRMS m/z 521.0882 (C₂₄H₂₂BrF₂N₂O₄ requires 521.0882).

Examples 188-193

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the general method for the preparation of Example 187 and substituting the appropriate carboxylic acid for methoxyacetic acid, the compounds of Examples 188-193 are prepared. These compounds were triturated with water and again with ether and purified by chromatography (silica gel, hexane/ethyl acetate) as appropriate to yield off-white solids. Example 191 was prepared from its N-t-butoxycarbonyl protected intermediate. Deprotection was accomplished with 4N HCl in dioxane to afford the title compound as its hydrochloride salt (86 mg, 24%). Deprotection of the methyl ester from Ex. 188 was accomplished with K₂CO₃ in methanol/water to yield Ex. 192 as a white solid. The yields and analytical data are shown below.

Compound		%		M + H	ESHRMS
No.	R	Yield	MF	Requires	m/z
Ex. 188	CH2OCOCH3	49	C25H23BrF2N2O5	549.0831	549.0849
Ex. 189	C(CH3)2OH	13	C25H25BrF2N2O4	535.1039	535.1035
Ex. 190	C(—CH2CH2—)OH	33	C25H23BrF2N2O4	535.0865	535.0876
Ex. 191	CH2NH2	24	C23H22BrF2N3O3	533.0882	533.0899
Ex. 192	CH2OH	25	C23H21BrF2N2O4	507.0726	507.0730
Ex. 193	CH2NHCOCH3	81	C25H24BrF2N3O3	548.0991	548.1000

Example 194

Preparation of 1-{4-[(4-acetylpiperazin-1-yl)carbonyl]benzyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

3-bromo-4-(2,4-difluorophenoxy)-6-methyl-1-[4-(piperazin-1-ylcarbonyl)benzyl]pyridin-2(1H)-one (200 mg, 0.36 mmol) was dissolved in N,N-dimethylformamide (5 mL). N,N-Diisopropylethylamine (0.25 mL, 1.44 mmol) was added followed by acetic anhydride (0.10 mL, 1.06 mmol). The reaction was stirred for 2 hours at ambient temperature. and concentrated to an oil that was triturated in ether and again in water to yield an off-white solid (131 mg, 63%) ¹H NMR (400 MHz, CD₃OD) δ 7.62 (app q, J=8.0 Hz, 1H); 7.42 (d, J=8.0 Hz, 2H), 7.23 (d, J=8.0 Hz, 2H), 7.62-7.02 (m, 1H); 7.02 (app t, J=8.0 Hz, 1H); 6.52 (s, 1H), 5.46 (s, 2H), 5.30 (s, 2H); 3.80-3.65 (m, 8H); 2.37 (s, 3H); 2.11 (s, 3H). ES HRMS m/z 574.1150 (C₂₇H₂₆BrF₂N₃O₄ requires 574.1148).

Example 195

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(4-{[4-(methylsulfonyl)piperazin-1-yl]carbonyl}benzyl)pyridin-2(1H)-one

3-bromo-4-(2,4-difluorophenoxy)-6-methyl-1-[4-(piperazin-1-ylcarbonyl)benzyl]pyridin-2(1H)-one (300 mg, 0.54 mmol) was dissolved in N,N-dimethylformamide (5 mL). 4-Methylmorpholine (0.23 mL, 2.2 mmol) was added followed by methanesulfonyl chloride (0.10 mL, 1.33 mmol) and the reaction was stirred for 2 h. The reaction was then diluted with tetrahydrofuran (40 mL) and polyamine resin (1.3 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (1 g, 1.38 mmol/g) were added. The mixture was shaken for 16 hours, filtered, and the resulting filtrate concentrated to an oil that was triturated with water. The resulting white solid was collected, washed with ether and dried (172 mg, 52%). ¹H NMR (400 MHz, CDCl₃) δ 7.57 (app q, J=8.2 Hz, 1H); 7.34 (d, J=8.0 Hz, 2H), 7.20 (d, J=8.0 Hz, 2H), 7.02 (app dt, J=1.2, 8.8 Hz, 1H), 6.88-6.82 (m, 1H); 6.02 (s, 1H), 5.37 (s, 2H), 5.21 (s, 2H); 3.80-3.20 (m, 8H); 2.79 (s, 3H); 2.30 (s, 3H). ES HRMS m/z 610.0851 (C₂₆H₂₆BrF₂N₃O₅S requires 610.0817).

Example 196

Preparation of methyl-4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzoate

Step 1. Preparation of 4-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]benzonitrile. 4-benzyloxy-2(1H)-pyridone (12.00 g, 59.63 mmol) was dissolved in dimethyl sulfoxide (100 mL). Potassium carbonate (10.99 g, 79.50 mmol) was added, followed by 4-fluorobenzonitrile (4.81 g, 39.75 mmol). The reaction was stirred at 100° C. for 18 hours. After cooling to room temperature the reaction was diluted with H₂O (150 mL) and the solids were collected by filtration washing with diethyl ether. Chromatography (silica gel, hexanes/ethyl acetate) provided an off-white solid (7.78 g, 65%). ¹H NMR (300 MHz, CDCl₃) δ 7.79 (d, J=8.3 Hz, 2H), 7.54 (d, J=8.5 Hz, 2H), 7.44-7.41 (m, 5H), 7.22 (d, J=13.3, 1H), 6.13 (dd, J=2.6, 7.7 Hz, 1H), 6.06 (d, J=2.6 Hz, 1H), 5.07 (s, 2H).

Step 2. Preparation of 4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzonitrile. 4-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]benzonitrile (Step 1) (2.76 g, 9.13 mmol) was suspended in acetonitrile (50 mL) and cooled in an ice-bath. N-bromosuccinimide (1.71 g, 9.54 mmol) was added. Once the addition was complete the cooling bath was removed. After stirring for 45 minutes the reaction was diluted with acetonitrile and solids were collected by filtration to give a white solid (3.13 g, 90%). ¹H NMR (300 MHz, DMSO-d₆) δ 8.00 (d, J=8.5 Hz, 2H), 7.84 (d, J=7.9 Hz, 1H), 7.66 (d, J=8.5, 2H), 7.50-7.37 (m, 5H), 6.63 (d, J=7.9 Hz, 1H), 5.41 (s, 2H).

Step 3. Preparation of methyl-4-[4-(benzyl)oxy-3-bromo-2-oxopyridin-1(2H)-yl]benzoate. 4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzonitrile (Step 2) (1.50 g, 3.93 mmol) suspended in methanol (50 mL) was cooled in an ice-bath. HCl (g) was then bubbled through the mixture for 5 minutes. The reaction was then stirred at room temperature overnight, at which time the reaction mixture was concentrated. The residue was suspended in 6N HCl (60 mL) and heated at reflux for 1.5 hours. After cooling to room temperature the solids were collected by filtration. Chromatography (silica gel, hexanes/ethyl acetate) provided an off-white shiny solid (0.540 g, 61%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.04 (d, J=8.5 Hz, 2H), 7.81 (d, J=7.8 Hz, 1H), 7.55 (d, J=8.6 Hz, 2H), 7.47-7.39 (m, 5H), 6.57 (d, J=7.9 Hz, 1H), 5.38 (s, 2H), 3.86 (s, 3H). ES-HRMS m/z 416.0355 (M+H caldc for C₂₀H₁₆BrNO₄ requires 414.0341).

Example 197

Preparation of 4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzoic Acid

Product from Example 196 (0.460 g, 1.11 mmol) was dissolved in tetrahydrofuran (5.0 mL). Potassium trimethylsilanolate (0.285 g, 2.22 mmol) was added. The reaction was stirred at room temperature for 3 hours at which time H₂O (10 mL) was added. The aqueous reaction mixture was acidified (pH-3) with 1N HCl. The tetrahydrofuran was evaporated, additional H₂O (50 mL) was added and the aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine (50 mL), dried over Na₂SO₄, filtered and evaporated to provide a rust colored solid (0.444 g, 100%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.02 (d, J=8.6 Hz, 2H), 7.80 (d, J=7.8 Hz, 1H), 7.55 (d, J=8.6 Hz, 2H), 7.50-7.34 (m, SH), 6.57 (d, J=7.9 Hz, 1H), 5.38 (s, 2H). ES-HRMS m/z 400.0191 (M+H calcd for C₁₉H₁₄BrNO₄ requires 400.0184).

Example 198

Preparation of 4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzamide

Product from Step 2 of Example 196 (0.238 g, 0.624 mmol) was suspended in tert-butyl alcohol (3.0 mL). KF on 40 wt % Al₂O₃ (0.453 g, 3.12 mmol) was added. The reaction mixture was heated at reflux for 5 days. Additional KF on 40 wt % Al₂O₃ (0.453 g, 3.12 mmol) was added and heating was continued at reflux overnight. After cooling to room temperature chloroform and methanol were added and the solids were collected by filtration. Chromatography (reverse-phase, acetonitrile/H₂O) provided a tan solid (0.073 g, 30%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.07 (s, 1H), 7.95 (d, J=8.6 Hz, 2H), 7.79 (d, J=7.8 Hz, 1H), 7.47-7.34 (m, 7H), 6.56 (d, J=7.9 Hz, 1H), 5.38 (s, 2H). ES-HRMS m/z 399.0372 (M+H calcd for C₁₉H₁₅BrN₂O₃ requires 399.0344).

Example 199

Preparation of 1-[4-(aminomethyl)phenyl]-4-(benzyloxy)-3-bromopyridin-2(1H)-one

Product from Step 2 of Example 196 (1.25 g, 3.28 mmol) was dissolved in tetrahydrofuran (15 mL). Borane-dimethylsulfide (3.44 mL, 6.89 mmol, 2.0 M in tetrahydrofuran) was added and the mixture heated at reflux. After 14.5 hours the solvent was evaporated. 0.5M NaOH (50 mL) was added followed by ethyl acetate. The aqueous layer was neutralized with 1N HCl. Methanol saturated with HCl was added and the mixture was heated at reflux for 5 hours. After cooling to room temperature, diethyl ether was added and the solids were collected by filtration. The solids were treated with 4N HCl in dixoane (5 mL) and methanol (1 mL) at room temperature for 1 hour, at which time diethyl ether was added and the solids were collected by filtration to give a tan solid (0.920 g, 67%). ¹H NMR (300 MHz, DMSO-d₆) δ 8.67 (br s, 2H), 7.76 (d, J=7.6 Hz, 1H), 7.64 (d, J=8.3 Hz, 2H), 7.50-7.37 (m, 7H), 6.56 (d, J=7.6 Hz, 1H), 5.41 (s, 2H), 4.09 (br s, 2H). ES-HRMS m/z 385.0555 (M+H calcd for C₁₉H₁₇BrN₂O₂ requires 385.0552).

Example 200

Preparation of methyl-4-[3-chloro-4-[(2,4-diflurobenzyl)oxy]-2-oxypyridin-1(2H)-yl]benzoate

Step 1. Preparation of 4-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]benzonitrile. 4-benzyloxy-2(1H)-pyridone (50.0 g, 248.47 mmol) was dissolved in dimethyl sulfoxide (300 mL). Potassium carbonate (68.68 g, 496.94 mmol) was added, followed by 4-fluorobenzonitrile (31.60 g, 260.89 mmol). The reaction was stirred at 100° C. for 20 hours. After cooling to room temperature the reaction was diluted with H₂O (600 mL) and the solids were collected by filtration washing with diethyl ether. The solids were then washed with hot methanol to provide a tan solid (55.6 g, 74%). ¹H NMR (300 MHz, CDCl₃) δ 7.79 (d, J=8.3 Hz, 2H), 7.54 (d, J=8.5 Hz, 2H), 7.44-7.41 (m, 5H), 7.22 (d, J=13.3, 1H), 6.13 (dd, J=2.6, 7.7 Hz, 1H), 6.06 (d, J=2.6 Hz, 1H), 5.07 (s, 2H).

Step 2. Preparation of 1-[4-nitrilephenyl]-4-hydroxy-2(1H)-pyridinone. 4-[4-(benzyloxy)-2-oxopyridin-1(2H)-yl]benzonitrile (Step 1) (20.0 g, 66.15 mmol) was dissolved in methanol (300 mL). Ammonium formate (8.34 g, 132.3 mmol) was added followed by 5% Pd/C (6.62 g). The resulting mixture was heated at reflux for 20 minutes at which time the reaction began to exotherm. The reaction was allowed to cool to room temperature at which time it was filtered through a pad of Celite® washing with methanol. The filtrate was evaporated to provide a pale yellow solid (16.2 g, >100%). ¹H NMR (300 MHz, CDCl₃) δ 8.46 (s, 1H), 7.95 (d, J=8.5 Hz, 2H), 7.62 (d, J=8.5 Hz, 2H), 7.47 (d, J=7.7 Hz, 1H), 5.98 (dd, J=2.6, 7.7 Hz, 1H), 5.54 (d, J=2.4 Hz, 1H).

Step 3. Preparation of 4-[4-[(2,4-difluorobenzyloxy)]-2-oxopyridin-1(2H)-yl]benzonitrile. 1-[4-Nitrilephenyl]-4-hydroxy-2(1H)-pyridinone (Step 2) (16.2 g) was dissolved in N,N-dimethylformamide (100 mL). Potassium carbonate (10.06 g, 72.77 mmol) was added followed by α-bromo-2,4-difluorotoluene (8.91 mL, 69.46 mmol). The resulting mixture was heated to 65° C. for 1 hour. Additional α-bromo-2,4-difluorotoluene (4.25 mL, 33.08 mmol) was added. The resulting mixture was heated to 65° C. for 5 hours. Additional 0-bromo-2,4-difluorotoluene (2.12 mL, 16.54 mmol) was added. After stirring at 65° C. overnight the reaction was allowed to cool to room temperature. H₂O (300 mL) was added and the solid was collected by filtration. A portion (8.0 g) of the solids were washed with hot methanol to give a pale yellow solid (6.22 g, 78%). ¹H NMR (300 MHz, CDCl₃) δ 8.00 (d, J=8.5 Hz, 2H), 7.72-7.64 (m, 2H), 7.66 (d, J=8.5 Hz, 2H), 7.40-7.32 (m, 1H), 7.22-7.16 (m, 1H), 6.17-6.11 (m, 2H), 5.17 (s, 2H).

Step 4. Preparation of methyl-4-[4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzoate. 4-[4-[(2,4-difluorobenzyloxy)]-2-oxopyridin-1(2H)-yl]benzonitrile (Step 3) (2.00 g, 5.91 mmol) suspended in methanol (20 mL) and H₂0 (5 mL) was cooled in an ice-bath. HCl (g) was bubbled through the mixture until most of the solids dissolved. The resulting mixture was then heated at reflux for 3 hours. The reaction was then recooled in an ice-bath and HCl was bubbled through the mixture for 5 minutes. The mixture was heated at reflux for 2 hours and then the methanol was evaporated. Additional H₂O (50 mL) was added and the aqueous reaction mixture was extracted with ethyl acetate (50 mL) and tetrahydrofuran (50 mL). The combined organic layers were washed with brine (50 mL), dried over Na₂SO₄, filtered and evaporated. Chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) gave an off-white solid (0.630 g, 29%). ¹H NMR (300 MHz, DMF-d₆) δ 8.15 (d, J=8.5 Hz, 2H), 7.80 (app q, J=7.9 Hz, 1H), 7.74-7.67 (m, 1H), 7.68 (d, J=8.5 Hz, 2H), 7.42-7.34 (app dt, J=2.4, 9.0 Hz, 1H), 7.28-7.22 (m, 1H), 6.20 (dd, J=2.6, 7.6 Hz, 1H), 6.15 (d, J=2.4 Hz, 1H), 5.28 (s, 2H), 3.98 (s, 3H).

Step 5. Preparation of methyl-4-[3-chloro-4-[(2,4-diflurobenzyl)oxy]-2-oxypyridin-1(2H)-yl]benzoate. Methyl-4-[4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzoate (Step 4) (0.520 g, 1.40 mmol) was suspended in acetonitrile (10.0 mL). N-chlorosuccinimide (0.196 g, 1.47 mmol) was added followed by several drops of dichloroacetic acid. The resulting mixture was heated at reflux overnight. After cooling to room temperature additional acetonitrile was added and the precipitate was collected by filtration to give an off-white solid (0.331 g, 58%). ¹H NMR (300 MHz, DMF-d₆) δ 8.34 (d, J=8.5 Hz, 2H), 8.12 (d, J=7.9 Hz, 1H), 8.04-7.96 (m, 1H), 7.88 (d, J=8.5 Hz, 2H), 7.59-7.53 (m, 1H), 7.52-7.41 (m, 1H), 7.05 (d, J=7.9 Hz, 1H), 5.70 (s, 2H), 4.15 (s, 3H). ES-HRMS m/z 406.0644 (M+H calcd for C₂₀H₁₄ClF₂NO₄ requires 406.0652).

Example 201

Preparation of 3-bromo-4-[(2,4-diflurorbenzyl)oxy]-1-[3-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one

Step 1. Preparation of 4-hydroxy-1-[3-(hydroxymethyl)phenyl]6-methylpyridin-2(1H)-one. 4-hydroxy-6-methyl-2-pyrone (10.0 g, 79.3 mmol) and 3-aminobenzyl alcohol (9.77 g, 79.3 mmol) were combined in H₂O (100 mL) and heat at reflux. After 48 hours at reflux the reaction mixture was concentrated. The residue was treated with methanol and the precipitate was collected by filtration to give a pale yellow solid (3.04 g, 17%). ¹H NMR (300 MHz, DMSO-d₆) d 10.6 (br s, 1H), 7.46-7.35 (m, 2H), 7.09-7.03 (m, 2H), 5.88 (d, J=1.6 Hz, 1H), 5.55 (d, J=2.6 Hz, 1H), 4.54 (d, J=4.2 Hz, 2H), 1.83 (s, 3H).

Step 2. Preparation of 1-[3-(hydroxymethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. 4-Hydroxy-1-[3-(hydroxymethyl)phenyl]6-methylpyridin-2(1H)-one (Step 1) (0.674 g, 2.91 mmol) was suspended in acetone (10 mL). Cesium carbonate (1.04 g, 3.21 mmol) was added followed by α-bromo-2,4-difluorotoluene (0.392 mL, 3.06 mmol). After stirring at room temperature for 2 days the reaction was concentrated. The residue was portioned between H₂O (30 mL) and ethyl acetate (30 mL). The aqueous layer was further extracted with ethyl acetate (30 mL). The combined organic layers were washed with brine (30 mL), dried over Na₂SO₄, filtered and concentrated. Chromatography (on silica, hexanes/ethyl acetate with 10% methanol) provided a white solid (0.531 g, 51%). ¹H NMR (300 MHz, CDCl₃) δ 7.51-7.39 (m, 3H), 7.82 (s, 1H), 7.16 (d, J=26.8 Hz, 1H), 7.08-6.86 (m, 2H), 6.00 (d, J=2.6 Hz, 1H), 5.92 (d, J=2.6 Hz, 1H), 5.05 (s, 2H), 4.68 (s, 2H), 1.93 (s, 3H). ES-HRMS m/z 358.1256 (M+H calcd for C₂₀H₁₇F₂NO₃ requires 358.1249).

Step 3. Preparation of 3-bromo-4-[(2,4-diflurorbenzyl)oxy]-1-[3-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one. 1-[3-(hydroxymethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (Step 2) (0.460 g, 1.29 mmol) was suspended in acetonitrile (5.0 mL) and cooled in an ice-bath. N-bromosuccinimide (0.241 g, 1.35 mmol) was added. Once the addition was complete the cooling bath was removed. After stirring for 1.5 hours the reaction was diluted with acetonitrile and solids were collected by filtration to give a white solid (0.385 g, 68%). ¹H NMR (300 MHz, DMSO-d₆) d 7.70 (app q, J=7.9 Hz, 1H), 7.49-7.32 (m, 3H), 7.24-7.10 (m, 3H), 6.66 (s, 1H), 5.35 (s, 2H), 4.56 (d, J=5.6 Hz, 2H), 1.95 (s, 3H). ES-HRMS m/z 436.0384 (M+H calcd for C₂₀H₁₆BrF₂NO₃ requires 436.0354).

Example 202

Preparation of methyl-4-[3-bromo-4-[(difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate

Step 1. Preparation of methyl 4-(4-hydroxy-6-methyl-2-oxypyridin-1(2H)-yl)benzoate. 4-Hydroxy-6-methyl-2-pyrone (21.00 g, 166.70 mmol) and 4-methylaminobenzoate (25.20 g, 166.70 mmol) were combined in 1,2-dichlorobenzene (50 mL) and rapidly heated to 160° C. After 15 minutes at 160° C. the reaction was allowed to cool to room temperature. The reaction was diluted with dichloromethane (50 mL) and extracted with saturated Na₂CO₃ (2×100 mL). The combined aqueous layers were acidified (pH-2) with concentrated HCl. The precipitate was collected by filtration and washed with diethyl ether to give a yellow/orange solid (10.9 g, 25%). ¹H NMR (300 MHz, DMSO-d₆) δ 10.8 (s, 1H), 8.07 (d, J=8.5 Hz, 2H), 7.40 (d, J=8.5 Hz, 2H), 5.95 (d, J=2.4 Hz, 1H), 5.61 (d, J=2.4, 1H), 3.91 (s, 3H), 1.85 (s, 3H).

Step 2. Preparation of methyl-4-[4-[(difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate. Methyl 4-(4-hydroxy-6-methyl-2-oxypyridin-1(2H)-yl)benzoate (Step 1) (10.90 g, 42.04 mmol) was dissolved in N,N-dimethylformamide (100 mL). Potassium carbonate (6.97 g, 50.45 mmol) was added, followed by 2,4-difluorobenzyl bromide (5.66 mL, 44.14 mmol). The reaction was stirred at room temperature for 3 days then diluted with H₂O (100 mL). The reaction mixture was extracted into ethyl acetate and tetrahydrofuran (2×100 mL). The precipitate was collected by filtration and the organic filtrate was washed with brine (50 mL), dried over Na₂SO₄, filtered and evaporated. The resulting solid was combined with the precipitate to provide a pale pink solid (6.77 g, 42%). ¹H NMR (300 MHz, DMSO-d₆) δ 8.01 (d, J=8.3 Hz, 2H), 7.67 (q, J=7.9 Hz, 1H), 7.43 (d, J=8.3 Hz, 2H), 7.35 (m, 1H), 7.18 (app dt, J=1.6, 8.5 Hz, 1H), 6.08 (d, J=1.8 Hz, 1H), 5.98 (d, J=2.4 Hz, 1H), 5.14 (s, 2H), 3.91 (s, 3H), 1.87 (s, 3H).

Step 3. Preparation of methyl-4-[3-bromo-4-[(difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate. Methyl-4-[4-[(difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (Step 2) (6.74 g, 17.49 mmol) suspended in acetonitrile (100 mL) was cooled in an ice-bath. N-bromosuccinimide (3.27 g, 18.36 mmol) was added. After 1 hour the ice-bath was removed and after an additional 30 minutes the reaction was diluted with acetonitrile (20 mL). The precipitate was collected by filtration to provide the title compound as an off-white solid (6.94 g, 85%). ¹H NMR (300 MHz, CDCl₃) δ 8.20 (d, J=8.7 Hz, 2H), 7.61 (q, J=7.9 Hz, 1H), 7.30 (d, J=8.7 Hz, 2H), 7.02-6.96 (m, 1H), 6.90 (app dt, J=2.4, 9.5 Hz, 1H), 6.14 (s, 1H), 5.28 (s, 2H), 3.98 (s, 3H), 2.00 (s, 3H). ES-HRMS m/z 464.0304 (M+H calcd for C₂₁H₁₆BrF₂NO₄ requires 464.0301).

Example 203

Preparation of 4-[3-bromo-4-[(difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic Acid

Product from Example 202 (7.43 g, 16.00 mmol) was dissolved in tetrahydrofuran (40 mL). Potassium trimethylsilanolate (4.10 g, 32.00 mmol) was added and the reaction mixture was stirred at room temperature for 22 hours. The tetrahydrofuran was evaporated and H₂O (50 mL) was added. The aqueous reaction mixture was acidified with 1N HCl and the precipitate was collected by filtration. The solids were washed with boiling methanol to give an off-white solid (5.05 g, 70%). ¹H NMR (300 MHz, DMSO-d₆) δ 13.2 (br s, 1H), 8.10 (d, J=8.5 Hz, 2H), 7.72 (q, J=7.9 Hz, 1H), 7.45 (d, J=8.3 Hz, 2H), 7.38 (app dt, J=2.4, 9.9 Hz, 1H), 7.23 (app dt, J=1.8, 8.5 Hz, 1H), 6.72 (s, 1H), 5.37 (s, 2H), 1.97 (s, 3H). ES-HRMS m/z 450.0154 (M+H calcd for C₂₀H₁₄BrF₂NO₄ requires 450.0147).

Example 204

Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-(trifluoromethyl)pyridin-2(1H)-one

The starting material (0.250 g, 0.591 mmol) was dissolved in 1-methyl-2-pyrrolidinone (5.0 mL). Trifluoroacetic acid, sodium salt (0.322 g, 2.36 mmol) was added, followed by copper(I)iodide (0.225 g, 1.18 mmol). The resulting mixture was heated to 180° C. for 5 hours and then allowed to cool to room temperature. The reaction was diluted with H₂O (50 mL) and brine (50 mL), then extracted into ethyl acetate (2×50 mL). The combined organic layers were washed with brine (50 mL), dried over Na₂SO₄, filtered and evaporated. Chromatography (reverse-phase, acetonitrile/H₂O) provided an off-white solid (0.050 g, 22%). ¹H NMR (400 MHz, CDCl₃) δ 7.40-7.27 (m, 8H), 7.06 (d, J=7.7 Hz, 1H), 6.97 (d, J=9.0 Hz, 1H), 6.07 (d, J=7.7 Hz, 1H), 5.20 (s, 2H), 5.06 (s, 2H). ES-HRMS m/z 378.1097 (M+H calcd for C₂₀H₁₅F₄NO₂ requires 378.1112).

Example 205

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic Acid

Product from Example 153 (50.0 g, 104.54 mmol) was dissolved in methanol (500 mL) and dioxane (100 mL). 1N NaOH (130 mL, 130 mmol) was added. The resulting mixture was heated to 50° C. for 5.5 hours. The reaction was partially concentrated and the heterogenous mixture was acidified (pH 2) with 1N HCl. The precipitate was collected by filtration to afford a white solid (49.2 g, >100%). ¹H NMR (300 MHz, DMSO-d₆) δ 7.94 (d, J=8.3 Hz, 2H), 7.70 (app q, J=7.9 Hz, 1H), 7.35 (dt, J=2.2, 9.9 Hz, 1H), 7.18 (app d, J=8.3 Hz, 2H), 7.17-7.12 (m, 1H), 6.64 (s, 1H), 5.41 (s, 2H), 5.33 (s, 2H), 2.32 (s, 3H). ES-HRMS m/z 464.0327 (M+H calcd for C₂₁H₁₆BrF₂NO₄ requires 464.0304).

Example 206

Preparation of 3-bromo-4-[(2,4-diflurobenzyl)oxy]-1-[4-(hydroxymethyl)benzyl]-6-methylpyridin-2(1H)-one

Product from example 205 (40.0 g, 86.16 mmol) suspended in tetrahydrofuran (300 mL) was cooled in an ice-bath. Borane dimethylsulfide (129.2 mL, 258.48 mmol, 2.0 M in tetrahydrofuran) was slowly added. The resulting mixture was slowly allowed to warm to room temperature overnight. The mixture was recooled in an ice-bath and quenched by the addition of small pieces of ice. After the evolution of gas ceased additional ice-water was added. The flask was fitted with a distillation apparatus and the dimethylsulfide was removed. After the reaction was cooled to room temperature, H₂O (300 mL), ethyl acetate (200 mL) and tetrahydrofuran (300 mL) were added. The precipitate that formed was collected by filtration and the filtrate was placed in a separatory funnel. The aqueous layer was further extracted with ethyl acetate (300 mL). The combined organic layers were washed with brine (300 mL). The organic phase was dried over Na₂SO₄ and evaporated which was combined with the precipitate to yield an off-white solid (37.8 g, 97%). ¹H NMR (400 MHz, CDCl₃) δ 7.47 (app q, J=7.7 Hz, 1H), 7.23 (d, J=7.9 Hz, 2H), 7.05 (d, J=7.9 Hz, 2H), 6.86 (app dt, J=2.3, 8.6 Hz, 1H), 6.79 (app dt, J=2.4, 8.4 Hz, 1H), 6.00 (s, 1H), 5.28 (s, 2H), 5.16 (s, 2H), 4.57 (s, 2H), 2.25 (s, 3H). ES-HRMS m/z 450.0512 (M+H calcd for C₂₁H₁₈BrF₂NO₃ requires 450.0511).

Example 207

Preparation of 3-bromo-4-[(2,4-diflurobenzyl)oxy]-1-[4-(1-hydroxy-1-methylethyl)benzyl]-6-methylpyridin-2(1H)-one

Preparation of 3-bromo-4-[(2,4-diflurobenzyl)oxy]-1-[4-(1-hydroxy-1-methylethyl)benzyl]-6-methylpyridin-2(1H)-one. Product from Example 153 (2.00 g, 4.18 mmol) suspended in tetrahydrofuran (20 mL) was cooled in the dry ice/acetone bath. Methyl magnesium bromide (4.32 mL, 12.96 mmol, 3.0 M in diethyl ether) was slowly added. The reaction was slowly allowed to warm to room temperature overnight. The reaction was then cooled in an ice bath and quenched by the addition of saturated NH₄Cl (50 mL). H₂O was added and the reaction was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na₂SO₄, filerted and evaporated. The residue was subjected to chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) to provide an off-white foam. The foam was dissolved in acetonitrile and cooled in an ice bath. N-bromosuccinimide (0.057 g, 0.320 mmol) was added. Once the addition was complete the cooling bath was removed. After 2.5 hours at room temperature the reaction was concentrated. Purification by chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) provided a white foam. ¹H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=7.7 Hz, 1H), 7.39 (d, J=78.3 Hz, 2H), 7.11 (d, J=8.2 Hz, 2H), 6.92 (app dt, J=1.7, 8.4 Hz, 1H), 6.86-6.81 (m, 1H), 5.97 (s, 1H), 5.31 (s, 2H), 5.18 (s, 2H), 2.29 (s, 3H), 1.52 (s, 6H). ES-HRMS m/z 478.0811 (M+H C₂₃H₂₂BrF₂NO₃ requires 478.0824).

Example 208

Preparation of 3-bromo-4-[(2,4-diflurobenzyl)oxy]-6-methyl-1-{4-[(methylamino)methyl]benzyl}pyridin-2(1H)-one

Step 1. Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzaldehyde. Product from Example 206 (1.30 g, 2.89 mmol) was suspended in acetonitrile (10 mL) and cooled in an ice-bath. 1-hydroxy-1,3-dihydro-3,3-bis(trifluoromethyl)-1,2-benziodoxole 1-oxide (0.580 g, 1.44 mmol) was added and the reaction mixture was stirred at room temperature overnight. Diethyl ether was added and the solid was collected by filtration to give a white solid (1.14 g, 88%). ¹H NMR (400 MHz, CDCl₃) δ 9.96 (s, 1H), 7.80 (d, J=8.2 Hz, 2H), 7.56 (app q, J=7.7 Hz, 1H), 7.30 (d, J=8.2 Hz, 2H), 6.93 (app dt, J=1.6, 8.3 Hz, 1H), 6.87-6.82 (m, 1H), 6.02 (s, 1H), 5.41 (s, 2H), 5.20 (s, 2H), 2.27 (s, 3H).

Step 2. 3-Bromo-4-[(2,4-diflurobenzyl)oxy]-6-methyl-1-{4-[(methylamino)methyl]benzyl}pyridin-2(1H)-one. 4-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzaldehyde (Step 1) (1.53 g, 3.41 mmol) of step 1 was dissolved in N,N-dimethylformamie (5.0 mL). Methylamine (3.41 mL, 6.83 mmol, 2.0 M in tetrahydrofuran) was added followed by NaHB(OAc) 3 (2.17 g, 10.23 mmol) in N,N-dimethylformamide (8.0 mL) and acetic acid (2.0 mL). The reaction was stirred at room temperature overnight at which time 1N NaOH (50 mL) was added and then extracted with ethyl acetate (2×50 mL). The organic layers were washed with brine (25 mL), dried over Na₂SO4 and evaporated. Chromatography (on silica, ethyl acetate with 5% methanolic ammonia/hexanes) afforded a tan solid (0.810 g, 53%). ¹H NMR (400 MHz, CDCl₃) δ 7.55 (app q, J=7.8 Hz, 1H), 7.22 (d, J=8.1 Hz, 2H), 7.11 (d, J=8.1 Hz, 2H), 6.92 (app dt, J=2.4, 8.3 Hz, 1H), 6.90-6.80 (m, 1H), 5.95 (s, 1H), 5.32 (s, 2H), 5.17 (s, 2H), 3.68 (s, 2H), 2.40 (s, 3H), 2.27 (s, 3H). ES-HRMS m/z 463.0838 (M+H calcd for C₂₂H₂₁BrF₂N₂O₄ requires 463.0827).

Example 209

Preparation of 4-[(2,4-diflurobenzyl)oxy]-1-(4-methoxybenzyl)-6-methylpyridin-2-(1H)-one

Step 1. Preparation of 1-(4-methoxybenzyl)-4-hydroxy-6-methylpyridin-2(1H)-one. 4-Hydroxy-6-methyl-2-pyrone (4.60 g, 36.45 mmol) and 4-methoxybenzylamine (5.00 g, 36.45 mmol) in H₂O (100 mL) were heated to reflux. After 15 hours at reflux the reaction was allowed to cool to room temperature. The precipitate was collected by filtration washing with H₂O to give a pale yellow solid (8.00 g, 89%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.2 (d, J=8.7 Hz, 2H), 6.85 (d, J=8.7 Hz, 2H), 5.74 (d, J=2.0 Hz, 1H), 5.56 (d, J=2.5 Hz, 1H), 5.08 (s, 2H), 3.68 (s, 3H), 2.14 (s, 3H).

Step 2. Preparation of 4-[(2,4-diflurobenzyl)oxy]-1-(4-methoxybenzyl)-6-methylpyridin-2(1H)-one. 1-(4-methoxybenzyl)-4-hydroxy-6-methylpyridin-2(1H)-one (Step 1) (7.97 g, 32.49 mmol) was dissolved in N,N-dimethylformamide (60 mL). Potassium carbonate (4.94 g, 35.74 mmol) was added, followed by □-bromo-2,4-difluorotoluene (4.38 mL, 34.11 mmol). The reaction was stirred at room temperature for 20 hours at which time the mixture was filtered through a pad of Celite® washing with acetonitrile and the filtrate was evaporated. The residue was dissolved in H₂O (150 mL) and extracted into ethyl acetate (2×100 mL). The organic phase was washed with brine (100 mL), dried over Na₂SO₄, filtered and evaporated. Chromatography (on silica, hexanes/ethyl acetate with 10% methanol) yielded an off-white solid (3.64 g, 30%). ¹H NMR (300 MHz CDCl₃) δ 7.42 (app q, J=7.7 Hz, 1H), 7.13 (d, J=8.5 Hz, 2H), 6.96-6.84 (m 2H), 6.85 (app d, J=8.7 Hz, 2H), 6.01 (d, J=2.6 Hz, 1H), 5.82 (d, J=2.8 Hz, 1H), 5.23 (s, 2H), 5.02 (s, 2H), 3.79 (s, 3H), 2.25 (s, 3H). ES-HRMS m/z 372.1412 (M+H C₂₁H₁₉F₂NO₃ requires 372.1417).

Example 210

Preparation of 3-bromo-4-[(2,4-diflurobenzyl)oxy]-1-(4-methoxybenzyl)-6-methylpyridin-2(1H)-one

Product from Example 209 (0.200 g, 0.538 mmol) suspended in acetonitrile (3 mL) was cooled in an ice-bath. N-bromosuccinimide (0.101 g, 0.565 mmol) was added. Once the addition was complete the cooling bath was removed. After 1 hour the reaction was concentrated. Purification by chromatography (silica gel, hexanes/ethyl acetate) provided a white solid (0.240 g, 99%). ¹H NMR (300 MHz, CDCl₃) δ 7.59 (app q, J=7.8 Hz, 1H), 7.16 (d, J=8.7 Hz, 2H), 6.97 (app dt, J=2.4, 8.6 Hz, 1H), 6.91-6.83 (m, 1H), 6.85 (app d, J=8.7 Hz, 2H), 5.98 (s, 1H), 5.31 (s, 2H), 5.21 (s, 2H), 3.79 (s, 3H), 2.34 (s, 3H). ES-HRMS m/z 450.0491 (M+H C₂₁H₁₈BrF₂NO₃ requires 450.0511).

Example 211

Preparation of 3-bromo-4-[(2,4-diflurobenzyl)oxy]-1-(4-hydroxybenzyl)-6-methylpyridin-2(1H)-one

Product from Example 210 (0.235 g, 0.522 mmol) was suspended in acetonitrile (3 mL). Cerric ammonium nitrate (1.14 g, 2.09 mmol) dissolved in H₂O (1 mL) was added. The reaction was stirred at room temperature for 1 hour and then diluted with dichloromethane (25 mL). The reaction was then washed with H₂O (10 mL). The aqueous phase was back extracted with dichloromethane (20 mL). The combined organic layers were dried over Na₂SO₄, filtered and evaporated. The residue was washed with hot ethyl acetate to give an off-white solid (0.134 g, 59%). ¹H NMR (300 MHz, DMSO-d₆) δ 7.75 (app q, J=7.9 Hz, 1H), 7.65 (s, 1H), 7.45-7.36 (m, 1H), 7.36 (d, J=10.1 Hz, 2H), 7.27-7.20 (m, 1H), 6.49 (d, J=10.1 Hz, 2H), 5.60 (s, 2H), 5.07 (s, 2H), 2.63 (s, 3H). ES-HRMS m/z 436.0187(M+H C₂₀H₁₆BrF₂NO₃ requires 436.0354).

Example 212

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1{4-[(4-hydroxy-4-methylpiperidin-1-yl)carbonyl]benzyl}-6-methylpyridin-2(1H)-one

Step 1. Preparation of 4-hydroxy-4-methylpiperidine hydrochloride. tert-Butyl-4-oxo-1-piperidine (10.0 g, 50.19 mmol) dissolved in diethyl ether (100 mL) was cooled in an ice-bath. Methyl magnesium bromide (18.40 mL, 55.21 mmol, 3.0 M in diethyl ether) was added. After slowly warming to room temperature the reaction was recooled in an ice-bath and quenched by the addition of saturated NH₄Cl (75 mL). Additional H₂O was added and the organic layer was removed. The aqueous layer was further extracted with diethyl ether (50 mL). The combined organic layers were washed with brine, dried over Na₂SO₄, filtered and concentrated. Chromatography (silica gel, hexanes/ethyl acetate) provided a clear oil. The resulting oil was dissolved in diethyl ether (10 mL) and treated with 4N HCl/dioxane (32.61 mL, 130.43 mmol). After stirring at room temperature for 1 hour the reaction mixture was concentrated to give a pale yellow solid (5.05 g, >100%).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1{4-[(4-hydroxy-4-methylpiperidin-1-yl)carbonyl]benzyl}-6-methylpyridin-2(1H)-one. Product from Example 205 (0.300 g, 0.646 mmol) was suspended in dichloromethane (6.0 mL). 1-hydroxybenzotriazole (0.044 g, 0.323 mmol) was added followed by 3-(1-cyclohexylcarbodiimide)propyl-functionalized silica gel (2.02 g, 1.29 mmol, loading=0.64 mmol/g), 3-(1-morpholine)propyl functionalized silica gel (1.84 g, 1.29 mmol, loading=0.7 mmol/g) and dichloromethane (2 mL). After stirring at room temperature for 15 minutes, 4-hydroxy-4-methylpiperidine hydrochloride (0.147 g, 0.969 mmol) was added. The resulting mixture was stirred at room temperature overnight, at which time dimethylamine-3-functionalized silica gel (1.7 g, 2.58 mmol, loading=1.5 mmol/g) was added followed by isocyanate-3-functionalized silica gel (1.3 g, 1.62 mmol, loading=1.22 mmol/g). The resulting mixture was stirred at room temperature for 3 hours. The reaction mixture was then filtered and concentrated. Chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) provided a white foam (0.200 g, 55%). ¹H NMR (300 MHz, CDCl₃) δ 7.58 (app q, J=7.7 Hz, 1H), 7.33 (d, J=8.1 Hz, 2H), 7.18 (d, J=8.1 Hz, 2H), 6.96 (app t, J=8.3 Hz, 1H), 6.87 (app dt, J=2.0, 9.5 Hz, 1H), 6.06 (s, 1H), 5.38 (s, 2H), 5.22 (s, 2H), 4.27 (br m, 1H), 3.41 (br m, 3H), 2.30 (s, 3H), 2.06 (s, 1H), 1.60 (br m, 4H), 1.28 (s, 3H). ES-HRMS m/z 561.1173 (M+H C₂₇H₂₇BrF₂N₂O₄ requires 561.1195).

Example 213

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxypyridin-1(2H)-yl]methyl}-N-(2-hydroxy-2-methylpropyl)benzamide

The title compound was by a procedure essentially as in Example 212 using 1-amino-2-methyl-2-propanol hydrochloride as starting material. ¹H NMR (400 MHz, CDCl₃) δ 7.70 (d, J=8.3 Hz, 2H), 7.53 (app q, J=7.8 Hz, 1H), 7.33 (t, J=5.8 Hz, 1H), 7.06 (d, J=8.3 Hz, 2H), 6.95-6.90 (m, 1H), 6.86-6.81 (m, 1H), 6.04 (s, 1H), 5.30 (s, 2H), 5.19 (s, 2H), 3.40 (d, J=5.9 Hz, 2H), 2.98 (br s, 1H), 2.24 (s, 3H), 1.21 (s, 6H). ES-HRMS m/z 535.1012 (M+H C₂₅H₂₅BrF₂N₂O₄ requires 535.1039).

Example 214

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1{4-[(4-hydroxypiperidin-1-yl)carbonyl]benzyl}-6-methylpyridin-2(1H)-one

The title compound was produced essentially as in Example 212 using 4-hydroxypiperidine as starting material. ¹H NMR (400 MHz, CDCl₃) δ 7.55 (app q, J=7.7 Hz, 1H), 7.30 (d, J=8.2 Hz, 2H), 7.15 (d, J=8.3 Hz, 2H), 6.94 (app dt, J=2.4, 8.4 Hz, 1H), 6.84 (app ddd, J=2.6, 8.9, 10.3 Hz, 1H), 6.01 (s, 1H), 5.36 (s, 2H), 5.19 (s, 2H), 4.12-4.07 (m, 1H), 3.96-3.90 (m, 1H), 3.60 (br s, 1H), 3.33 (br s, 1H), 3.13 (br s, 1H), 2.27 (s, 3H), 1.91 (br s, 3H), 1.77 (br s, 1H), 1.57 (br s, 1H), 1.44 (br s, 1H). ES-HRMS m/z 547.1006 (M+H C₂₆H₂₅BrF₂N₂O₄ requires 547.1039).

Example 215

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)benzamide

To a reaction vessel (borosilicate culture tube) was added product from Example 205 (0.300 g, 0.646 mmol). A stock solution of 1-hydroxybenzotriazole in N,N-dimethylformamide (3 mL, 0.11 M) was added to the reaction vessel followed by approximately 1.10 g of the polymer bound carbodiimide resin (1.8 mmol/g). Additional N,N-dimethylformamide (2 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. Ethanolamine (0.06 mL, 0.994 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with tetrahydrofuran (20 mL) and treated with approximately 2.0 g of polyamine resin (2.63 mmol/g) and approximately 2.6 g of methylisocyanate functionalized polystyrene (1.10 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 3 hours. The reaction vessel was then opened and the solution phase product was separated from the insoluble quenched byproducts by filtration and collection into a vial. After partially evaporation the insoluble byproducts were rinsed further with tetrahydrofuran (2×10 mL) and combined with the partially reduced filtrate. The resulting filtrate was concentrated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor) to give an off-white solid. (0.111 g, 34%) ¹H NMR (400 MHz, DMF-d₆) δ 8.45 (t, J=5.4 Hz, 1H), 7.94 (d, J=8.2 Hz, 2H), 7.76 (app q, J=7.9 Hz, 1H), 7.33-7.27 (m, 1H), 7.27 (app d, J=7.9 Hz, 2H), 7.20 (app dt, J=2.4, 8.6 Hz, 1H), 6.65 (s, 1H), 5.47 (s, 2H), 5.38 (s, 2H), 4.83 (br s, 1H), 3.64-3.60 (m, 2H), 2.47-3.42 (m, 2H), 2.40 (s, 3H). ES-HRMS m/z 507.0742 (M+H C₂₃H₂₁BrF₂N₂O₄ requires 507.0726).

Examples 216-231

Preparation of 3-bromo-4-(2,4-difluorophenoxy)-6-methyl-1-[4-(aminocarbonyl)benzyl]pyridin-2(1H)-one Compounds

By following the method of Example 215 and substituting the appropriate amine, the compounds of Examples 216-231 are prepared. The deprotection of the protected intermediates was accomplished with 4N HCl in dioxane to afford the compounds as hydrochloride salts.

Compound			%		M + H	ESHRMS
No.	R1	R2	Yield	MF	Requires	m/z
Ex. 216	CH2CH2NH—	CH2CH2NH—	73	C25H24BrF2N3O4	532.1042	532.1024
Ex. 217	H	CH2CH2NH2	49	C23H22BrF2N3O3	506.0885	506.0883
Ex. 218	H	CH2CH2CH2NH2	31	C24H24BrF2N3O3	520.1042	520.1042
Ex. 219	H	OH	53	C21H17BrF2N2O4	479.0413	479.0423
Ex. 220	H	CH3	59	C22H19BrF2N2O4	477.0620	477.0605
Ex. 221	CH3	CH3	51	C23H21BrF2N2O3	491.0776	491.0794
Ex. 222	CH2CH2O—	CH2CH2O—	61	C25H23BrF2N2O4	533.0882	533.0901
Ex. 223	CH2CH2OH	CH2CH2OH	69	C25H25BrF2N2O5	551.0988	551.0978
Ex. 224	CH2CH2CH2—	CH2CH2CH2—	66	C26H25BrF2N2O3	531.1084	531.1089
Ex. 225	H	CH(CH3)2	50	C24H23BrF2N2O3	505.0933	505.0901
Ex. 226	CH2CH2—	CH2CH2—	71	C25H23BrF2N2O3	517.0933	517.0908
Ex. 227	CH2CH2N(CH3)—	CH2CH2N(CH3)—	83	C26H26BrF2N3O3	546.1198	546.1215
Ex. 228	H	CH2CH2N(CH3)2	81	C25H26BrF2N3O3	534.1198	534.1197
Ex. 229	H	CH2CH2OCH3	79	C24H23BrF2N2O4	521.0882	521.0861
Ex. 230	CH3	CH2CH2OH	36	C24H23BrF2N2O4	521.0882	521.0893
Ex. 231	CH3	CH2CH2OCH3	82	C25H25BrF2N2O4	535.1039	535.1028

Example 232

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)benzamide

To a reaction vessel (borosilicate culture tube) was added EXAMPLE 203 (0.300 g, 0.666 mmol). A stock solution of 1-hydroxybenzotriazole in N,N-dimethylformamide (3 mL, 0.11 M) was added to the reaction vessel followed by approximately 1.13 g of the polymer bound carbodiimide resin (1.8 mmol/g). Additional N,N-dimethylformamide (2 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. Ethanolamine (0.06 mL, 0.994 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with tetrahydrofuran (20 mL) and treated with approximately 2.0 g of polyamine resin (2.63 mmol/g) and approximately 2.7 g of methylisocyanate functionalized polystyrene (1.10 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 3 hours. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partially evaporation the insoluble byproducts were rinsed further with tetrahydrofuran (2×10 mL) and combined with the partially reduced filtrate. The resulting filtrate was concentrated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor). Purification by chromatography (silica gel) provided an off-white solid (0.155 g, 47%). ¹H NMR (400 MHz, DMF-d₆) δ 8.58 (t, J=5.5 Hz, 1H), 8.10 (d, J=8.3 Hz, 2H), 7.79 (app q, J=7.9 Hz, 1H), 7.47 (d, J=8.3 Hz, 2H), 7.36-7.30 (m, 1H), 7.21 (app dt, J=2.4, 8.5 Hz, 1H), 6.73 (s, 1H), 5.43 (s, 2H), 3.68 (app t, J=5.9 Hz, 2H), 3.52-3.49 (m, 2H), 2.03 (s, 3H). ES-HRMS m/z 493.0597 (M+H C₂₂H₁₉BrF₂N₂O₄ requires 493.0569).

Example2 233-243

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the method of Example 232 and substituting ethanolamine for the appropriate amine, the compounds of Examples 233-243 are prepared. The deprotection of the protected intermediates was accomplished with 4N HCl in dioxane to afford the compounds as hydrochloride salts.

Compound			%		M + H	ESHRMS
No.	R1	R2	Yield	MF	Requires	m/z
Ex. 233	CH2CH2NH—	CH2CH2NH—	40.3	C24H22BrF2N3O3	518.0885	518.0866
Ex. 234	H	CH2CH2NH2	57.1	C22H20BrF2N3O3	492.0729	492.0748
Ex. 235	H	CH2CH2CH2NH2	21.5	C23H22BrF2N3O3	506.0885	506.0915
Ex. 236	H	OH	33.9	C20H15BrF2N2O4	465.0256	465.0259
Ex. 237	H	CH3	20.7	C21H17BrF2N2O3	463.0463	463.0479
Ex. 238	CH3	CH3	22.3	C22H19BrF2N2O3	477.0620	477.0643
Ex. 239	CH2CH2O—	CH2CH2O—	84.4	C24H21BrF2N2O4	519.0726	519.0723
Ex. 240	CH2CH2OH	CH2CH2OH	46.6	C24H23BrF2N2O5	537.0831	537.0854
Ex. 241	CH2CH2CH2—	CH2CH2CH2—	76.5	C25H23BrF2N2O3	517.0933	517.0892
Ex. 242	H	CH(CH3)2	52.6	C23H21BrF2N2O3	491.0776	491.0781
Ex. 243	CH2CH2—	CH2CH2—	47.2	C24H21BrF2N2O4	503.0776	503.0791

Example 244

Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide

Product from Example 203 (0.500 g, 1.11 mmol) was suspended in tetrahydrofuran (5.0 mL). 2-Chloro-4,6-dimethoxy-1,3,5-triazine (0.234 g, 1.33 mmol) was added followed by 4-methylmorpholine (0.366 mL, 3.33 mmol). The resulting mixture was stirred at room temperature for 1.5 hours at which time NH₄OH (2.5 mL) was added. The resulting mixture was stirred at room temperature overnight. H₂O (25 mL) and tetrahydrofuran (25 mL) was added. The aqueous layer was further extracted with ethyl acetate (25 mL). The combined organic layers were washed with saturated sodium carbonate solution (25 mL), 1N HCl (25 mL), brine (25 mL), dried over Na₂SO₄, filtered and concentrated to provide a pale yellow solid (0.500 g, 100%). ¹H NMR (400 MHz, DMF-d₆) δ 8.13 (s, 1H), 8.02 (d, J=8.5 Hz, 2H), 7.70 (app q, J=7.9 Hz, 1H), 7.40 (d, J=8.5 Hz, 2H), 7.41-7.34 (m, 1H), 7.22 (app dt, J=1.8, 8.5 Hz, 1H), 6.71 (s, 1H), 5.37 (s, 2H), 1.97 (s, 3H). ES-HRMS m/z 449.0281 (M+H C₂₀H₁₅BrF₂N₂O₃ requires 449.0307).

Example 245

Preparation of 4-(benzyloxy)-3-bromo-1-[4-(morpholin-4-ylcarbonyl)phenyl]pyridin-2(1H)-one

To a reaction vessel (borosilicate culture tube) was added product from Example 197 (0.100 g, 0.250 mmol) which was dissolved in N,N-dimethylformamide (2.0 mL). 1-Hydroxybenzotriazole (0.017 g, 0.125 mmol) was added to the reaction vessel followed by approximately 0.423 g of the polymer bound carbodiimide resin (1.8 mmol/g). Additional N,N-dimethylformamide (2 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. Morpholine (0.033 g, 0.0.375 mmol) dissolved in N,N-dimethlyformamide (0.5 mL) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with N,N-dimethylformamide (2.0 mL) and dichloromethane (4.0 mL) and treated with approximately 0.770 g of polyamine resin (2.63 mmol/g) and approximately 1.0 g of methylisocyanate functionalized polystyrene (1.10 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 3 hours. The reaction vessel was then opened and the solution phase product was separated from the insoluble quenched byproducts by filtration and collection into a vial. After partially evaporation the insoluble byproducts were rinsed with dichloromethane (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor) to give an off-white solid (0.092 g, 79%). ¹H NMR (400 MHz, CDCl₃) δ 7.50 (d, J=8.5 Hz, 2H), 7.48-7.33 (m, 7H), 7.27 (d, J=7.8 Hz, 1H), 6.19 (d, J=7.8 Hz, 1H), 5.29 (s, 2H), 3.76-3.47 (br m, 8H). ES-HRMS m/z 469.0733 (M+H C₂₃H₂₁BrN₂O₄ requires 469.0757).

Example 246

Preparation of 4-(benzyloxy)-3-bromo-1-[4-(piperazin-1-ylcarbonyl)phenyl]pyridin-2(1H)-one Hydrochloride

By following the method of Example 245 and substituting N-tert-butyl carboxylate piperazine (0.070 g, 0.375 mmol) for morpholine the title compound was prepared as the N-t-butoxycarbonyl protected compound. The deprotection of the N-t-butoxycarbonyl intermediate was accomplished with 4N HCl in dioxane to afford the title compound as its hydrochloride salt (0.112 g, >100%). ¹H NMR (400 MHz, DMSO-d₆) δ 9.55 (br s, 2H), 7.78 (d, J=7.8 Hz, 1H), 7.58 (d, J=8.5 Hz, 2H), 7.48-7.33 (m, 7H), 6.57 (d, J=7.8 Hz, 1H), 5.38 (s, 2H), 3.79-3.36 (br m, 4H), 3.30-3.14 (br s, 4H). ES-HRMS m/z 468.0940 (M+H C₂₃H₂₂BrN₃O₃ requires 468.0917).

Example 247

Preparation of 4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]-N-hydoxybenzamide

By following the method of Example 245 and substituting O-(tetrahydro-2H-pyranyl-2yl) hydroxylamine (0.044 g, 0.375 mmol) for morpholine the title compound was prepared as the tetrahydropyranly protected compound. The deprotection of the tetrahydropyranly intermediate was accomplished with 4N HCl in dioxane to afford the title compound (0.056 g, >71%). ¹H NMR (400 MHz, DMSO-d₆) δ 11.03 (br s, 1H), 7.83 (d, J=8.6 Hz, 2H), 7.78 (d, J=7.8 Hz, 1H), 7.48-7.35 (m, 7H), 6.55 (d, J=7.8 Hz, 1H), 5.37 (s, 2H). ES-HRMS m/z 415.0278 (M+H C₁₉H₁₅BrN₂O₄ requires 415.0288).

Example 248

Preparation of methyl-4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoate

Step 1. Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpridin-2(1H)-one. 4-(2,4-Difluoro-benzyloxy)-1H-pyridin-2-one (5.00 g, 19.90 mmol) was suspended in 1,2-dichloroethane (100 mL). Dichloroacetic acid (0.082 mL, 0.995 mmol) was added, followed by N-chlorosuccinimide (3.19 g, 23.88 mmol). The reaction mixture was heated at 80° C. for 15.5 hours. The 1,2-dichloroethane was evaporated and the remaining solids were washed with acetonitrile to provide a tan solid (4.97 g, 88%).

Step 2. Preparation of methyl-4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoate. 3-Chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpridin-2(1H)-one (Step 1) (4.97 g, 17.40 mmol) suspended in tetrahydrofuran (50 mL) was cooled in an ice-bath. Methyl 4-(bromomethyl)benzoate (5.98 g, 26.10 mmol) was added, followed by sodium hydride (0.835 g, 20.88 mmol, 60% dispersion in mineral oil). Once the addition was complete the cooling bath was removed in the mixture was heated to 50° C. for 19 hours. After cooling to room temperature saturated NH₄Cl (50 mL) was added. Ethyl acetate was added and the precipitate was collected by filtration. The filtrate was further extracted with ethyl acetate. The combined organic layers were washed with brine (50 mL), dried over Na₂SO₄, filtered and evaporated. The resulting solid was combined with the precipitate and washed with hot ethyl acetate to give an off-white solid (5.24 g, 69%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.90 (d, J=8.5 Hz, 2H), 7.63 (app q, J=7.9 Hz, 1H), 7.31 (app dt, J=2.4, 9.9 Hz, 1H), 7.21 (d, J=8.3 Hz, 2H), 7.17-7.13 (m, 1H), 6.60 (s, 1H), 5.36 (s, 2H), 5.27 (s, 2H), 3.81 (s, 3H), 2.27 (s, 3H). ES-HRMS m/z 434.0931 (M+H C₂₂H₁₈BrF₂NO₄ requires 434.0965).

Example 249

Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methylbenzamide

To a reaction vessel (borosilicate culture tube) was added product from Example 169 (0.300 g, 0.646 mmol). A stock solution of 1-hydroxybenzotriazole in N,N-dimethylformamide (3 mL, 0.11 M) was added followed by approximately 1.10 g of the polymer bound carbodiimide resin (1.8 mmol/g). Additional N,N-dimethylformamide (2 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. N-Methylamine (0.50 mL, 0.999 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with tetrahydrofuran (35 mL) and treated with approximately 2.0 g of polyamine resin (2.63 mmol/g) and approximately 2.6 g of methylisocyanate functionalized polystyrene (1.50 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 4 hours. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with tetrahydrofuran (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor). Chromatography (C-18, acetonitrile/H₂O with 0.1% trifluoroacetic acid) afforded a white solid (0.178 g, 58%). ¹H NMR (400 MHz, DMF-d₆) δ 7.65-7.53 (m, 3H), 7.37-7.28 (m, 2H), 6.97-6.82 (m, 2H), 6.00 (s, 1H), 5.36 (s, 2H), 5.19 (s, 3H), 2.96 (t, J=4.83 Hz, 3H), 2.29 (s, 3H). ES-HRMS m/z 477.0635 (M+H C₂₂H₁₉BrF₂N₂O₃ requires 477.0620).

Examples 250-261

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the method of Example 249 and replacing N-methylamine with the appropriate amine, the compounds of Examples 250-261 are prepared. The deprotection of the protected intermediates was accomplished with 4N HCl in dioxane to afford the compounds as hydrochloride salts.

						ES-
Compound			%		M + H	HRMS
No.	R1	R2	Yield	MF	Requires	m/z
Ex. 250	CH2CH2NH—	CH2CH2NH—	89	C25H24BrF2N3O4	532.1042	532.1067
Ex. 251	H	CH2CH2NH2	75	C23H22BrF2N3O3	506.0885	506.0900
Ex. 252	H	CH2CH2CH2NH2	84	C24H24BrF2N3O3	520.1042	520.1000
Ex. 253	H	OH	45	C21H17BrF2N2O4	479.0413	479.0394
Ex. 254	CH3	CH3	69	C23H21BrF2N2O3	491.0776	491.0731
Ex. 255	H	CH3	58	C22H19BrF2N2O3	479.0602	479.0598
Ex. 256	CH2CH2O—	CH2CH2O—	69	C25H23BrF2N2O4	533.0882	533.0857
Ex. 257	H	CH2CH2OH	51	C23H21BrF2N2O4	507.0726	507.0698
Ex. 258	CH2CH2OH	CH2CH2OH	25	C25H25BrF2N2O5	551.0988	551.0972
Ex. 259	CH2CH2CH2—	CH2CH2CH2—	62	C26H25BrF2N2O3	531.1089	531.1088
Ex. 260	H	CH(CH3)2	46	C24H23BrF2N2O3	505.0933	505.0918
Ex. 261	CH2CH2—	CH2CH2—	60	C25H23BrF2N2O3	517.0933	517.0950

Example 262

Preparation of N-(3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-2-methoxyacetamide

To a reaction vessel (borosilicate culture tube) was added methoxyacetic acid (0.09 g, 1.00 mmol). A stock solution of 1-hydroxybenzotriazole (3 mL, 0.16 M) and N-methylmorpholine (3 mL, 0.43 M) in N,N-dimethylformamide were added to the reaction vessel followed by approximately 0.97 g of the polymer bound carbodiimide resin (1.38 mmol/g). Additional N,N-dimethylformamide (3 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 4 hours. 1-[3-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (EXAMPLE 161) (0.30 g, 0.668 mmol) was then added to the reaction vessel followed by additional N,N-dimethylformamide (5.0 mL) and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with tetrahydrofuran (20 mL) and treated with approximately 2.06 g of polyamine resin (2.63 mmol/g) and approximately 2.67 g of methylisocyanate functionalized polystyrene (1.10 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 4 hours. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with tetrahydrofuran (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor) afforded a tan solid (0.321 g, 89.4%). ¹H NMR (400 MHz, DMF-d₆) δ 8.33 (br s, 1H), 7.81 (app q, J=7.85 Hz, 1H), 7.40-7.23 (m, 5H), 7.09 (d, J=7.25 Hz, 1H), 6.68 (s, 1H), 5.46 (s, 2H), 5.42 (s, 2H), 4.45 (d, J=6.24 Hz, 2H), 3.93 (s, 2H), 3.39 (s, 3H), 2.44 (s, 3H). ES-HRMS m/z 521.0891 (M+H C₂₄H₂₃BrF₂N₂O₄ requires 521.0882).

Example 263-265

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the method of Example 262 and replacing methoxyacetic acid with the appropriate acid, the compounds of Examples 263-265 are prepared. The deprotection of the protected intermediates was accomplished with 4N HCl in dioxane to afford the compounds as hydrochloride salts.

Compound		%		M + H	ES-HRMS
No.	R	Yield	MF	Requires	m/z
Ex. 263	CH2NH2	46.1	C23H23BrF2N3O3	506.0885	506.0870
Ex. 264	CH2NHCOCH3	70.4	C25H24BrF2N3O4	548.0991	548.1007
Ex. 265	CH2OCOCH3	42.7	C23H21BrF2N2O4	549.0831	549.0837

Example 266

Preparation of N-(3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-2-hydroxy-2-methylpropanamide

1-[3-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (Example 161) (0.300 g, 0.668 mmol), 1-hydroxyisobutyric acid (0.215 g, 2.064 mmol), 1-hydroxybenzotriazole (0.112 g, 0.826 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.185 g, 0.963 mmol) were dissolved in N,N-dimethylacetamide (3 mL). N-methylmorpholine (0.209 g, 2.064 mmol) was added, and the reaction stirred for 1 hour at room temperature. The reaction was diluted with H₂O (50 mL) and the aqueous layer extracted with ethyl acetate (3×25 mL). The combined organics were then washed with 1N HCl (25 mL), saturated Na₂CO₃ (25 mL), brine (25 mL), dried over Na₂SO₄, and concentrated to yield an off-white solid (0.235 g, 64%). ¹H NMR (400 MHz, DMF-d₆) δ 8.25 (br s, 1H), 7.81 (app q, J=7.92 Hz, 1H), 7.40-7.21 (m, 5H), 7.09 (d, J=6.84 Hz, 1H), 6.67 (s, 1H), 5.46 (s, 2H), 5.42 (s, 2H), 4.42 (d, J=6.24 Hz, 2H), 2.44 (s, 3H), 1.38 (s, 6H). ES-HRMS m/z 535.1024 (M+H C₂₅H₂₅BrF₂N₂O₄ requires 535.1039).

Example 267A

Preparation of N-(3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-1-hydroxycyclopropanecarboxamide

By following the method of Example 266 and substituting 1-hydroxy-1-cyclopropane-carboxylic acid for 1-hydroxyisobutyric acid, the title compound was prepared (0.352 g, 96%). ¹H NMR (400 MHz, DMF-d₆) δ 8.46 (app t, J=6.24 Hz, 1H), 7.81 (app q, J=7.92 Hz, 1H), 7.40-7.22 (m, 5H), 7.06 (d, J=7.05 Hz, 1H), 6.67 (s, 1H), 5.45 (s, 2H), 5.42 (s, 2H), 4.46 (d, J=6.44 Hz, 2H), 2.45 (s, 3H), 1.17-1.12 (m, 2H), 0.93 (app q, J=3.82 Hz, 2H). ES-HRMS m/z 533.0861 (M+H C₂₅H₂₃BrF₂N₂O₄ requires 533.0882).

Example 267B

Preparation of N′-(3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N,N-dimethylurea

Step 1. Preparation of 4-nitrophenyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzylcarbamate 1-[3-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (Example 161) (2.00 g, 4.45 mmol) was suspended in dichloromethane (15 mL). Pyridine was added (0.43 mL, 5.34 mmol). After stirring for 10 minutes at room temperature, a stock solution of 4-nitrophenyl chloroformate (10.0 mL, 0.50 M) in dichloromethane was added dropwise. After stirring for 4.5 hours at room temperature, a stock solution of 4-nitrophenyl chloroformate (2.5 mL, 0.50 M) in dichloromethane was again added dropwise and stirring continued at 40° C. overnight. The reaction mixture was concentrated and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) to afford a yellow solid (1.11 g, 66%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.56 (app t, J=6.10 Hz, 1H), 8.24-8.21 (m, 2H), 7.62 (app q, J=7.88 Hz, 1H), 7.40-7.27 (m, 7H), 6.98 (d, J=7.52 Hz, 1H), 6.54 (s, 1H), 5.30 (s, 2H), 5.24 (s, 2H), 4.25 (d, J=6.18 Hz, 2H), 2.30 (s, 3H). ES-HRMS m/z 614.0753 (M+H C₂₈H₂₂BrF₂N₃O₆ requires 614.0733).

Step 2. Preparation of N′-(3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N,N-dimethylurea. To a reaction vessel (borosilicate culture tube) was added 4-nitrophenyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzylcarbamate (from step 1) (0.350 g, 0.570 mmol) dissolved in dichloromethane (6.0 mL). The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. A stock solution of N,N-dimethylamine in tetrahydorfuran (0.427 mL, 2.0 M) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. The reaction mixture was concentrated and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) which afforded an off white solid (0.226 g, 63.3%). ¹H NMR (400 MHz, DMF-d₆) δ 7.81 (app q, J=7.92 Hz, 1H), 7.40-7.19 (m, 5H), 7.06 (d, J=7.45 Hz, 1H), 6.88 (app t, J=5.84 Hz, 1H), 6.68 (s, 1H), 5.45 (s, 2H), 5.42 (s, 1H), 4.35 (d, J=5.84 Hz, 1H), 2.92 (s, 6H), 2.44 (s, 3H). ES-HRMS m/z 520.1065 (M+H C₂₄H₂₄BrF₂N₃O₃ requires 520.1042).

Examples 268-70

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the method of Example 267 and replacing N,N-dimethylamine with the appropriate amine, the compounds of Examples 268-270 are prepared. The deprotection of the protected intermediates was accomplished with 4N HCl in dioxane to afford the compounds as hydrochloride salts.

						ES-
Compound			%		M + H	HRMS
No.	R1	R2	Yield	MF	Requires	m/z
Ex. 268	CH2CH2N—	CH2CH2N—	66.6	C26H27BrF2N4O3	561.1307	561.1309
Ex. 269	H	CH3	27.0	C23H22BrF2N3O3	506.0885	506.0898
Ex. 270	CH2CH2O—	CH2CH2O—	64.4	C26H26BrF2N3O4	562.1148	562.1137

Example 271

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic Acid

Step 1: Preparation of methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate. Methyl 3-aminobenzoate (75.00 g, 496.13 mmol) and 4-hydroxy-6-methyl-2-pyrone (62.57 g, 496.13 mmol) were suspended in 1,2-dichlorobenzene (150 mL) and heated to 165° C. for 15 minutes. The reaction was cooled to room temperature and extracted with 0.54M K₂CO₃ (4×250 mL). The aqueous layers were acidified (pH 2) with 4N HCl. The precipitate was collected by filtration to afford a yellow-orange solid (20.24 g, 16%). The resulting filtrate was extracted with ethyl acetate (3×1 L). The organic layers were washed with brine (500 mL), dried over MgSO₄ and evaporated. The resulting solid was washed with hot H₂O to afford a yellow-orange solid (3.84 g, 3%). The two solids were then combined. ¹H NMR (400 MHz, DMSO-d₆) δ 7.98 (dt, J=1.31, 7.79 Hz, 1H), 7.69 (app t, J=1.78 Hz, 1H), 7.62 (t, J=7.78 Hz, 1H) 7.49 (ddd, J=1.07, 1.07, 7.85 Hz, 1H), 5.89 (dd, J=0.87, 2.48 Hz, 1H), 5.55 (app d, J=0.94 Hz, 1H), 3.83 (s, 3H), 1.80 (s, 3H). ES-HRMS m/z 260.0895 (M+H C₁₄H₁₃NO₄ requires 260.0917).

Step 2: Preparation of methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate. Methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate (from step 1) (24.00 g, 92.57 mmol) and K₂CO₃ (15.35 g, 111.08 mmol) were dissolved in NAN-dimethylformamide (220 mL). 2,4-Difluorobenzyl bromide (20.12 g, 97.20 mmol) was then added and the reaction mixture stirred for 48 hours at room temperature. The reaction mixture was diluted with H₂O (1 L) and the precipitate collected by filtration to afford a white solid (4.08 g, 11%). The resulting oil was purified by chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) to afford an off white solid (11.88 g, 33%). The two solids were combined. ¹H NMR (400 MHz, CDCl₃) δ 8.11 (dt, J=1.41, 7.79 Hz, 1H), 7.87 (app t, J=1.78 Hz, 1H), 7.58 (app t, J=7.69 Hz, 1H) 7.45-7.38 (m, 2H), 6.94-6.84 (m, 2H), 5.97 (d, J=2.68 Hz, 1H), 5.90 (ddd, J=0.94, 1.74, 1.74 Hz, 1H), 5.97 (s, 1H), 3.90 (s, 3H), 1.89 (s, 3H). ES-HRMS nm/z 386.1179 (M+H C₂₁H₁₇F₂NO₄ requires 386.1198).

Step 3: Preparation of methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate. Methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate from step 2) (15.85 g, 41.130 mmol) suspended in acetonitrile (165 mL) was cooled in an ice-bath. N-bromosuccinimide (7.687 g, 43.186 mmol) was added and the ice-bath was removed. The reaction mixture was stirred for 1.5 hours at room temperature. Reaction was concentrated and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) afforded an off white solid (17.63 g, 92%). ¹H NMR (400 MHz, CDCl₃) δ 8.17 (dt, J=1.41, 7.85 Hz, 1H), 7.90 (t, J=1.81 Hz, 1H), 7.67-7.41 (m, 3H), 7.05-6.88 (m, 2H), 6.13 (s, 1H), 5.30 (s, 2H), 3.95 (s, 1H), 2.01 (s, 3H). ES-HRMS m/z 464.0286 (M+H C₂₁H₁₆BrF₂NO₄ requires 464.0304).

Step 4: Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic acid. Methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (from step 3) (10.0 g, 21.539 mmol) was dissolved in methanol (36 mL) and tetrahydrofuran (14 mL). 4N NaOH (13.5 mL, 53.847 mmol) was added. The resulting mixture was stirred for 1.5 hours at room temperature. The reaction was acidified (pH 2) with 4N HCl. The precipitate was collected by filtration to afford an off white solid (7.83 g, 81%) ¹H NMR (400 MHz, DMSO-d₆) δ 8.01 (dt, J=1.41, 7.65 Hz, 1H), 7.76 (app t, J=1.78 Hz, 1H), 7.76-7.15 (m, SH), 6.66 (s, 1H), 5.32 (s, 2H), 1.92 (s, 3H). ES-HRMS m/z 450.0134 (M+H C₂₀H₁₄BrF₂NO₄ requires 450.0147).

Example 272

Preparation of Ethyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate

By following the method of Example 271 and substituting ethyl 3-aminobenzoate for methyl 3-aminobenzoate, the title compound was prepared (2.66 g, 79%). ¹H NMR (400 MHz, CDCl₃) δ 8.13 (dt, J=1.41, 7.85 Hz, 1H), 7.84 (t, J=1.88 Hz, 1H), 7.62-7.55 (m, 2H), 7.36 (app dq, J=1.07, 7.85 Hz, 1H), 6.96 (app dt, J=2.55, 8.35 Hz, 1H), 6.88-6.84 (m, 1H), 6.08 (s, 1H), 5.25 (s, 2H), 4.42-4.30 (m, 2H), 1.96 (s, 3H), 1.36 (t, J=7.12 Hz, 3H). ES-HRMS m/z 478.0482 (M+H C₂₂H₁₈BrF₂NO₄ requires 478.0460).

Example 273

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methylbenzamide

To a reaction vessel (borosilicate culture tube) was added Product from Example 271 (0.300 g, 0.666 mmol). A stock solution of 1-hydroxybenzotriazole in N,N-dimethylformamide (3 mL, 0.11 M) was added to the reaction vessel followed by approximately 0.97 g of the polymer bound carbodiimide resin (1.38 mmol/g). Additional N,N-dimethylformamide (2 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. N-Methylamine in tetrahydrofuran (0.50 mL, 0.999 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with tetrahydrofuran (30 mL) and treated with approximately 2.0 g of polyamine resin (2.63 mmol/g) and approximately 3.6 g of methylisocyanate functionalized polystyrene (1.10 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 4 hours. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with tetrahydrofuran (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor) to give an off-white solid (0.189 g, 61%). ¹H NMR (400 MHz, DMF-d₆) δ 8.56 (br d, J=4.16 Hz, 1H), 8.05-7.76 (m, 3H), 7.66 (t, J=7.79 Hz, 1H), 7.56-7.19 (m, 3H), 6.74 (s, 1H), 5.43 (s, 2H), 3.46 (s, 3H), 2.03 (s, 3H). ES-HRMS m/z 463.0476 (M+H C₂₁H₁₇BrF₂N₂O₃ requires 463.0463).

Examples 274-289

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the method of Example 273 and replacing N-methylamine with the appropriate amine, the compounds of Examples 274-289 are prepared. The deprotection of the protected intermediates was accomplished with 4N HCl in dioxane to afford the compounds as their hydrochloride salts.

Compound			%		M + H	ES-HRMS
No.	R1	R2	Yield	MF	Requires	m/z
Ex. 274	CH2CH2NH—	CH2CH2NH—	92.8	C24H22BrF2N3O3	518.0885	518.0865
Ex. 275	H	CH2CH2NH2	95.7	C22H20BrF2N3O3	492.0729	492.0711
Ex. 276	H	CH2CH2CH2NH2	97.8	C23H22BrF2N3O3	506.0885	506.0889
Ex. 277	H	OH	91.0	C20H15BrF2N2O4	465.0256	465.0278
Ex. 278	CH3	CH3	67.7	C22H19BrF2N2O3	477.0620	477.0626
Ex. 279	CH2CH2O—	CH2CH2O—	86.7	C24H21BrF2N2O4	519.0726	519.0696
Ex. 280	H	CH2CH2OH	78.3	C22H19BrF2N2O4	493.0569	493.0575
Ex. 281	CH2CH2CH2—	CH2CH2CH2—	87.9	C25H23BrF2N2O3	517.0933	517.0918
Ex. 282	H	CH(CH3)2	80.6	C23H21BrF2N2O3	491.0776	491.0797
Ex. 283	CH2CH2—	CH2CH2—	87.9	C24H21BrF2N2O4	503.0776	503.0732
Ex. 284	CH2CH2N(CH3)—	CH2CH2N(CH3)—	75.8	C25H24BrF2N3O3	532.1042	532.1038
Ex. 285	H	CH2CH2N(CH3)2	86.1	C24H24BrF2N3O3	520.1042	520.1030
Ex. 286	H	CH2CH2OCH3	90.2	C23H21BrF2N2O4	507.0726	507.0680
Ex. 287	CH3	CH2CH2N(CH3)2	60.0	C25H26BrF2N3O3	534.1198	534.1155
Ex. 288	CH3	CH2CH2OH	81.6	C23H21BrF2N2O4	507.0726	507.0694
Ex. 289	CH3	CH2CH2OCH3	94.4	C24H23BrF2N2O4	521.0882	521.0862

Example 290

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide

Product from Example 271 (2.00 g, 4.44 mmol) and 2-chloro-4,6-dimethoxy-1,3,5-triazine (0.94 g, 5.33 mmol) were suspended in tetrahydrofuran (20 mL). 4-Methylmorpholine (1.5 mL, 13.32 mmol) was added. The resulting mixture was stirred for 1.5 hours at room temperature. NH₄OH (10 mL, 148.00 mmol) was added and the reaction was stirred for 0.5 hours at room temperature. H₂O (50 mL) and tetrahydrofuran (50 mL) were added and the organic layer was separated. The aqueous phase was extracted with ethyl acetate (75 mL) and the combined organics were washed with saturated Na₂CO₃ (50 mL), 1N HCl (50 mL), and brine (50 mL). The organic phase was dried over Na₂SO₄ and evaporated. The resulting solid was washed with diethyl ether to give a white solid (1.86 g, 93%). ¹H NMR (400 MHz, DMF-d₆) δ 8.20 (br s, 1H), 8.10-8.07 (m, 1H), 7.79 (s, 1H), 7.79 (app q, J=7.83 Hz, 1H), 7.66 (app t, J=7.79 Hz, 1H), 7.57-7.54 (m, 1H), 7.46 (br s, 1H), 7.36-7.19 (m, 2H), 6.74 (s, 1H), 5.43 (s, 2H), 2.04 (s, 3H). ES-HRMS m/z 449.0307 (M+H C₂₀H₁₅BrF₂N₂O₃ requires 449.0307).

Example 291

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic Acid

Step 1. Preparation of methyl 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate Product from step 2, Example 271 (4.54 g, 11.78 mmol) and N-chlorosuccinimide (1.65 g, 12.37 mmol) were suspended in dichloromethane (12 mL). Dichloroacetic acid (0.10 ml, 1.22 mmol) was added and the reaction mixture was stirred overnight at 40° C. The reaction was cooled to room temperature and a precipitate formed. The precipitate was collected by filtration and washed with dichloromethane (3×10 mL) to afford a white solid (1.75 g, 35%). The filtrate was concentrated and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) to afforded an off white solid (1.29 g, 26%). The two solids were then combined. ¹H NMR (400 MHz, CDCl₃) δ 8.12 (dt, J=1.38, 7.83 Hz, 1H), 7.85 (t, J=1.74 Hz, 1H), 7.60-7.52 (m, 2H), 7.37 (dq, J=0.92, 7.92 Hz, 2H), 6.95 (app dt, J=2.55, 8.32 Hz, 1H), 6.89-6.83 (m, 1H), 6.11 (s, 1H), 5.24 (s, 2H), 3.90 (s, 3H), 1.96 (s, 3H). ES-HRMS nm/z 420.0783 (M+H C₂₁H₁₆ClF₂NO₄ requires 420.0809).

Step 2. Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic acid. Methyl 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (from step 1) (2.90 g, 6.91 mmol) was dissolved in methanol (5 mL) and tetrahydrofuran (12 mL). 4N NaOH (4.3 mL, 17.27 mmol) was added. The resulting mixture was stirred for 1.5 hours at room temperature. The reaction was acidified (pH-2) with 4N HCl. The precipitate was collected by filtration to afford an off white solid (2.36 g, 84%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.01 (dt, J=1.41, 7.65 Hz, 1H), 7.76 (app t, J=1.68 Hz, 1H), 7.69-7.53 (m, 3H), 7.36-7.14 (m, 2H), 6.69 (s, 1H), 5.32 (s, 2H), 1.93 (s, 3H). ES-HRMS m/z 406.0662 (M+H C₂₀H₁₄ClF₂NO₄ requires 406.0652).

Example 292

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[3-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one

The starting material (0.550 g, 1.540 mmol) and N-chlorosuccinimide (0.214 g, 1.602 mmol) were suspended in dichloromethane (15 mL). Dichloroacetic acid (0.01 ml, 0.154 mmol) was added and the reaction mixture heated to 40° C. for 9 hours. The reaction was cooled to room temperature and a precipitate formed. The precipitate was collected by filtration and washed with dichloromethane (3×10 mL) to afford a white solid (0.286 g, 47%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.38 (app q, J=7.35 Hz, 1H), 7.30-7.24 (m, 2H), 7.00 (br s, 1H), 6.85 (app dt, J=2.37, 6.24 Hz, 1H), 6.82-6.67 (m, 2H), 6.01 (s, 1H), 5.07 (s, 2H), 4.48 (d, J=5.24 Hz, 2H), 1.81 (app d, J=0.40 Hz, 3H). ES-HRMS m/z 392.0885 (M+H C₂₀H₁₆ClF₂NO₃ requires 392.0860).

Example 293

Preparation of 1-[3-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1. Preparation of 1-[3—(Chloromethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. 2,4,6-Trichloro-[1,3,5]-triazine (3.09 g, 16.78 mmol) was dissolved in N,N-dimethylformamide (45 mL). The reaction mixture was stirred at room temperature for 1 hour and then dichloromethane (90 mL) was added. The alcohol (5.72 g, 15.99 mmol) was then added. The reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with dichloromethane (200 mL) and the organic phase was washed with H₂O (200 mL), saturated Na₂CO₃ (200 mL), 1N HCl (200 mL), and brine (200 mL). The organic phase was dried over MgSO₄ and evaporated to give an orange solid (5.95 g, 99%).

Step 2. Preparation of 1-[3-(aminomethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. 1-[3—(Chloromethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one from step 1(1.00 g, 2.66 mmol) was suspended in methanol (5 mL). The suspension was then brought to −78° C. and NH₃ was bubbled through the reaction mixture for 10 minutes. The reaction was then slowly allowed to warm to room temperature and stirred at room temperature for 4 days. The reaction was concentrated and the residue taken up in CH₂Cl₂ and filtered to remove excess salt. The filtrate was concentrated to afford a tan solid (0.94 g, 99%).

Step 3. Preparation of 1-[3-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. 1-[3-(aminomethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one from step 3 (3.89 g, 10.93 mmol) suspended in acetonitrile (42 mL) was cooled in an ice-bath. N-bromosuccinimide (2.04 g, 11.47 mmol) was added and the ice-bath was removed. The reaction mixture was stirred for 1.5 hours at room temperature. The reaction was diluted with acetonitrile (100 mL) and the precipitate that formed was collected by filtration and washed with acetonitrile (3×30 mL) to afford an off-white solid (2.74 g, 58%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.67-7.59 (m, 3H), 7.34-7.31 (m, 2H), 7.04 (app t, J=8.72 Hz, 2H), 7.05-6.88 (m, 2H), 6.13 (s, 1H), 5.30 (s, 2H), 3.95 (s, 1H), 2.01 (s, 3H). ES-HRMS m/z 435.0538 (M+H C₂₀H₁₇BrF₂N₂O₂ requires 435.0514).

Example 294

Preparation of N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}methanesulfonamide

To a reaction vessel (borosilicate culture tube) was added product from Example 293 (0.200 g, 0.459 mmol) and N,N-dimethylformamide (4 mL). A stock solution of 4-methylmorpholine in N,N-dimethylformamide (1.8 mL, 1.0 M) was added to the reaction vessel and the parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 10 minutes. A stock solution of methanesulfonyl chloride in N,N-dimethylformamide (4.50 mL, 0.15 M) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature for 2 hours. At this time the reaction was diluted with dichloromethane (4 mL) and treated with approximately 2.1 g of polyamine resin (2.63 mmol/g) and approximately 0.8 g of methylisocyanate functionalized polystyrene (1.7 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature overnight. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with dichloromethane (2×5 mL). The filtrate was evaporated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor) to give a yellow solid (0.190 g, 81%). ¹H NMR (400 MHz, CD₃OD) δ 7.63 (app q, J=7.00 Hz, 1H), 7.56-7.50 (m, 2H), 7.25 (m, 1H), 7.16 (dt, J=1.94, 7.25 Hz, 1H), 7.04 (app, J=8.59 Hz, 2H), 6.58 (s, 1H), 5.34 (s, 2H), 4.30 (s, 2H), 2.87 (s, 3H), 2.03 (s, 3H). ES-HRMS m/z 513.0313 (M+H C₂₁H₁₉BrF₂N₂O₄S requires 513.0290).

Examples 295-96

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the method of Example 294 and replacing methanesulfonyl chloride with the appropriate acid chloride, the compounds of Examples 295-296 are prepared.

					ES-
Compound		%		M + H	HRMS
No.	R	Yield	MF	Requires	m/z
Ex. 295	CH3	78.0	C22H19BrF2N2O3	477.0620	477.0640
Ex. 296	OCH3	84.0	C22H19BrF2N2O4	493.0569	493.0591

Example 297

Preparation of N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-2-methoxyacetamide

To a reaction vessel (borosilicate culture tube) was added approximately 2.87 g of polymer bound carbodiimide resin (0.96 mmol/g) followed by a stock solution of methoxyacetic acid (8.0 mL, 0.10 M) in N,N-dimethylacetamide. A stock solution of 1-hydroxybenzotriazole in N,N-dimethylacetamide (3.0 mL, 0.10 M) and N-methylmorpholine (6.0 mL, 0.10 M) in 1,2-dichloroethane were added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 4 hours. A stock solution of the product from Example 293 in N,N-dimethylacetamide (5.0 mL, 0.10 M) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with 1,2-dichloroethane (10 mL) and treated with approximately 1.70 g of polyamine resin (2.63 mmol/g) and approximately 0.84 g of methylisocyanate functionalized polystyrene (1.50 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 4 hours. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with N,N-dimethylacetamide (2×5 mL). The filtrate was evaporated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor) and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) afforded an off white solid (0.081 g, 28%). ¹H NMR (400 MHz, DMF-d₆) δ 7.59 (q, J=7.65 Hz, 1H), 7.46 (app t, J=7.55 Hz, 1H), 7.40-7.37 (m, 1H), 7.11-7.07 (m, 2H), 7.00 (t, J=8.56 Hz, 2H), 6.54 (s, 1H), 5.30 (s, 2H), 4.43 (s, 2H), 3.88 (s, 2H), 3.35 (app d, J=0.80 Hz, 2H), 1.97 (s, 3H). ES-HRMS m/z 507.0699 (M+H C₂₃H₂₁BrF₂N₂O₄ requires 507.0726).

Examples 298-300

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the method of and replacing methoxyacetic acid with the appropriate acid, the compounds of Examples 298-300 are prepared. The deprotection of the protected intermediates was accomplished with 4N HCl in dioxane or 1 M K₂CO₃ in methanol to afford the compounds as hydrochloride salts.

					ES-
Compound		%		M + H	HRMS
No.	R	Yield	MF	Requires	m/z
Ex. 298	CH2OCOCH3	35.5	C24H21BrF2N2O5	535.0675	535.0686
Ex. 299	CH2NH2	32.6	C22H20BrF2N3O3	492.0729	492.0744
Ex. 300	CH2OH	33.4	C22H19BrF2N2O4	493.0569	493.0578

Example 301

Preparation of N′-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-N,N-dimethylurea

Step 1: Preparation of 4-nitrophenyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzylcarbamate. 1-[3-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (1.08 g, 2.48 mmol) was suspended in dichloromethane (7.5 mL). Pyridine was added (0.222 mL, 2.74 mmol). After stirring for 10 minutes at room temperature, a stock solution of 4-nitrophenyl chloroformate (5.0 mL, 0.50 M) in dichloromethane was added dropwise. After stirring for 4.5 hours at room temperature, a stock solution of 4-nitrophenyl chloroformate (2.5 mL, 0.50 M) in dichloromethane was again added dropwise and stirring continued at room temperature overnight. The reaction mixture was concentrated and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) afforded a yellow solid (0.85 g, 57%).

Step 2: Preparation of title compound. To a reaction vessel (borosilicate culture tube) was added 4-nitrophenyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzylcarbamate (from step 1) (0.150 g, 0.250 mmol) and dichloromethane (2.5 mL). The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. A stock solution of N,N-dimethylamine in tetrahydorfuran (0.15 mL, 2.0 M) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. The reaction mixture was concentrated and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) which afforded an off white solid (0.065 g, 51%). ¹H NMR (400 MHz, DMF-d₆) δ 7.58 (app q, J=7.79 Hz, 1H), 7.42 (app t, J=7.65 Hz, 1H), 7.37 (app d, J=7.79 Hz, 1H), 7.08 (s, 1H), 7.03 (app dt, J=1.58, 5.37 Hz, 1H), 6.96 (app dt, J=2.55, 8.39 Hz, 1H), 6.88-6.83 (m, 1H), 6.06 (s, 1H), 5.24 (s, 2H), 4.95 (app t, J=5.57 Hz, 1H), 4.42 (app dddd, J=5.10, 5.71, 10.20, 15.17 Hz, 2H), 2.90 (s, 6H), 1.96 (s, 3H). ES-HRMS m/z 506.0848 (M+H C₂₃H₂₂BrF₂N₃O₃ requires 506.0885).

Examples 302-303

Preparation of Compounds Corresponding in Structure to the Following Formula

By following the method of Example 301 and substituting N,N-dimethylamine with the appropriate amine, the compounds of Examples 302-303 are prepared.

						ES-
Compound			%		M + H	HRMS
No.	R1	R2	Yield	MF	Requires	m/z
Ex. 302	H	CH3	52.3	C22H20BrF2N3O3	492.0729	492.0737
Ex. 303	CH2CH2O—	CH2CH2O—	50.7	C25H24BrF2N3O4	548.0991	548.0962

Example 304

Preparation of N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}urea

To a reaction vessel (borosilicate culture tube) was added EXAMPLE 293 (0.200 g, 0.459 mmol) and tetrahydrofuran (4.0 mL). A stock solution of 4-methylmorpholine in tetrahydrofuran (1.8 mL, 1.0 M) was added to the reaction vessel and the parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 10 minutes. A stock solution of trimethylsilyl isocyanate in tetrahydrofuran (4.0 mL, 0.2 M) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature for two hours. At this time the reaction was diluted with tetrahydrofuran (4.0 mL) and the resulting precipitate collected by filtration. The solid was then washed with tetrahydrofuran (3×5 mL) to afford a white solid (0.214 g, 97%). ¹H NMR (400 MHz, CD₃OD) δ 7.72 (app q, J=7.83 Hz, 1H), 7.55 (app t, J=8.06 Hz, 1H), 7.46 (d, J=7.52 Hz, 1H), 7.25-7.14 (m, 4H), 6.65 (s, 1H), 5.65 (app t, J=0.80 Hz, 1H), 5.40 (s, 2H), 4.38 (s, 2H), 2.05 (s, 3H). ES-HRMS m/z 478.0594 (M+H C₂₁H₁₈BrF₂N₃O₃ requires 478.0572).

Example 305

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{3-[(dimethylamino)methyl]phenyl}-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-[(2,4-difluorobenzyl)oxy]-1-{3-[(dimethylamino)methyl]phenyl}-6-methylpyridin-2(1H)-one. 1-[3-(Chloromethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (from step 1 of the synthesis of EXAMPLE 293) (0.500 g, 1.330 mmol) was suspended in a stock solution of N,N-dimethylamine in methanol (2.0 mL, 2.0 M) and stirred overnight at room temperature. Reaction was concentrated and the residue partitioned between H₂O (25 mL) and ethyl acetate (25 mL). The aqueous layer was further extracted with ethyl acetate (2×30 mL), and the combined organics were washed with brine (30 mL), dried over MgSO₄, and concentrated to afford an off-white solid (0.508 g, 99%).

Step 2: Preparation of the title compound. 4-[(2,4-difluorobenzyl)oxy]-1-{3-[(dimethylamino)methyl]phenyl}-6-methylpyridin-2(1H)-one from step 1(0.200 g, 0.521 mmol) was suspended in acetonitrile (2.5 mL) and cooled in an ice-bath. N-bromosuccinimide (0.097 g, 0.547 mmol) was added and the ice-bath was removed. The reaction mixture was stirred for 1.5 hours at room temperature. The reaction was diluted with acetonitrile (100 mL). The precipitate that formed was collected by filtration and washed with acetonitrile (3×15 mL) to afford a yellow solid (0.160 g, 66%). Chromatography (C-18, acetonitrile/H₂O with 0.1% trifluoroacetic acid, followed by chromatography silica gel, ethyl acetate with 10% methanol/hexanes) afforded an off-white solid (0.024 g, 10%). ¹H NMR (400 MHz, CD₃OD) δ 7.68 (app q, J=7.85 Hz, 1H), 7.58 (app t, J=7.65 Hz, 1H), 7.50 (app d, J=7.85 Hz, 1H), 7.25-7.05 (m, 4H), 6.63 (s, 1H), 5.39 (s, 2H), 3.61 (app q, J=12.08 Hz, 2H), 2.32 (s, 6H), 2.08 (s, 3H). ES-HRMS m/z 463.0782 (M+H C₂₂H₂₁BrF₂N₂O₂ requires 463.0827).

Example 306

Preparation of N-{4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzyl}acetamide

1-[4-(aminomethyl)phenyl]-4-(benzyloxy)-3-bromopyridin-2(1H)-one hydrochloride (0.150 g, 0.389 mmol) was dissolved in N,N-dimethylformamide (3.5 mL). A stock solution of 4-methylmorpholine in N,N-dimethylformamide (1.5 mL, 1.0 M) was added and the reaction stirred at room temperature for 10 minutes. A stock solution of acetyl chloride in N,N-dimethylformamide (3.0 mL, 0.2 M) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at 200 RPM for 2 hours at room temperature. At this time the reaction was diluted with dichloromethane (4 mL) and treated with approximately 1.8 g of polyamine resin (2.63 mmol/g) and approximately 0.8 g of methylisocyanate functionalized polystyrene (1.7 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature overnight. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were further rinsed with dichloromethane (3×5 mL) and combined with the partially concentrated filtrate. The resulting filtrate was concentrated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor) to give an off-white solid (0.083 g, 50%). ¹H NMR (400 MHz, CD₃OD) δ 7.59 (d, J=7.79 Hz, 1H), 7.48-7.29 (m, 9H), 6.55 (d, J=7.79 Hz, 1H), 5.35 (s, 2H), 4.39 (s, 2H), 1.98 (s, 3H). ES-HRMS m/z 427.0625 (M+H C₂₁H₁₉BrN₂O₃ requires 427.0652).

Example 307

Preparation of N-{4-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]benzyl}-2-hydroxyacetamide

To a reaction vessel (borosilicate culture tube) was added approximately 1.95 g of polymer bound carbodiimide resin (0.96 mmol/g) followed by a stock solution of glycolic acid (5.8 mL, 0.10 M) in N,N-dimethylacetamide. A stock solution of 1-hydroxybenzotriazole in N,N-dimethylacetamide (0.4 mL, 0.10 M) and N-methylmorpholine in 1,2-dichloroethane (3.9 mL, 0.10 M) were added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 2 hours. A stock solution of 1-[4-(aminomethyl)phenyl]-4-(benzyloxy)-3-bromopyridin-2(1H)-one hydrochloride in N,N-dimethylacetamide (0.05 M, 7.8 mL) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with 1,2-dichloroethane (8 mL) and treated with approximately 1.17 g of polyamine resin (2.63 mmol/g) and approximately 0.58 g of methylisocyanate functionalized polystyrene (1.50 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 4 hours. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with N,N-dimethylacetamide (2×5 mL) and combined with the partially concentrated filtrate. The filtrate was concentrated by blowing N₂ over the vial while heating (60° C.) in a reaction block (KEM-Lab Parallel Reactor) and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) which afforded an off white solid (0.081 g, 21%). ¹H NMR (400 MHz, CD₃OD) δ 7.55-7.30 (m, 10H), 6.51 (d, J=7.85 Hz, 1H), 5.37 (s, 2H), 4.52 (s, 2H), 4.08 (s, 2H). ES-HRMS m/z 443.0605 (M+H C₂₁H₁₉BrN₂O₄ requires 443.0601).

Example 308

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-morpholin-4-ylethyl)pyridin-2(1H)-one

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.100 g, 0.303 mmol), cesium carbonate (0.296 g, 0.909 mmol), and 4-(2-chloroethyl)morpholine (0.059 g, 0.394 mmol) were suspended in acetonitrile (4 mL). The reaction was stirred at 60° C. overnight. H₂O (25 mL) was added and the resulting precipitate was collected by filtration. The solid was subjected to chromatography (silica gel, ethyl acetate with 10% methanol) afforded an off-white solid (0.040 g, 30%). ¹H NMR (400 MHz, CDCl₃) δ 7.55 (app q, J=7.92 Hz, 1H), 6.93 (app t, J=8.39 Hz, 1H), 6.84 (app t, J=9.40 Hz, 1H), 5.95 (s, 1H), 5.18 (s, 2H), 4.16 (app t, J=6.78 Hz, 2H), 3.68 (s, 4H), 2.65 (app t, J=6.38 Hz, 2H), 2.54 (s, 4H), 2.43 (s, 3H). ES-HRMS m/z 443.0743 (M+H C₁₉H₂₁BrF₂N₂O₃ requires 443.0776).

Example 309

Preparation of Ethyl 3-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]propanoate

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.50 g, 1.78 mmol) and cesium fluoride (0.0027 g, 0.178 mmol) were suspended in tetrahydrofuran (10 mL) followed by dropwise addition of tetraethylortho silicate (0.37 g, 1.78 mmol) at room temperature. After stirring for 10 minutes at room temperature, ethyl acrylate (0.23 g, 2.32 mmol) was added dropwise and the reaction stirred at room temperature overnight. The reaction mixture was filtered through a pad of Celite®. The filtrate was concentrated and the resulting residue subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) to afford a white solid (0.62 g, 92%). ¹H NMR (400 MHz, CDCl₃) δ 7.42 (d, J=7.79 Hz, 1H), 7.41-7.29 (m, 5H), 6.03 (d, J=7.65 Hz, 1H), 5.20 (s, 2H), 4.17 (t, J=5.98 Hz, 2H), 4.07 (q, J=7.16 Hz, 2H), 2.83 (t, J=5.98 Hz, 2H), 1.19 (t, J=7.18 Hz, 3H). ES-HRMS m/z 380.0523 (M+H C₁₇H₁₈BrNO₄ requires 380.0492).

Example 310

Preparation of Methyl 3-[4-(benzyloxy)-3-bromo-2-oxopyridin-1(2H)-yl]propanoate

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (5.00 g, 17.85 mmol) and cesium fluoride (0.27 g, 1.78 mmol) were suspended in tetrahydrofuran (50 mL) followed by dropwise addition of tetramethylortho silicate (2.70 g, 17.85 mmol) at room temperature. After stirring for 10 minutes at room temperature, methyl acrylate (2.00 g, 23.20 mmol) was added dropwise and the reaction stirred at room temperature for 48 hours. The reaction mixture was filtered through a pad of Celite®. The filtrate was concentrated and the resulting residue subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexanes) to afford a white solid (6.10 g, 93%). ¹H NMR (400 MHz, CDCl₃) δ 7.42 (d, J=7.65 Hz, 1H), 7.41-7.29 (m, 5H), 6.04 (d, J=7.65 Hz, 1H), 5.20 (s, 2H), 4.17 (t, J=5.91 Hz, 2H), 3.63 (s, 3H), 2.85 (t, J=5.91 Hz, 2H). ES-HRMS m/z 366.0350 (M+H C₁₆H₁₆BrNO₄ requires 366.0335).

Example 311

Preparation of N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-2,6-difluorobenzamide

Step 1. Preparation of 3,4-dibromo-1-(3-fluorobenzyl)pyridin-2(1H)-one 3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate (2.00 g, 4.65 mmol), KBr (5.53 g, 46.49 mmol), and 18-Crown-6 (0.10 g, 0.38 mmol) were dissolved in N,N-dimethylacetamide (26 mL). The reaction mixture was then heated at reflux for 16 hours. The reaction was concentrated and the resulting residue was partition between water (50 mL) and ethyl acetate (3×50 mL). The combined organics were washed with H₂O (2×30 mL), brine (50 mL), dried over MgSO₄, concentrated, and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexane) to afford a brown solid (0.850 g, 51%).

Step 2. Preparation of 4-azido-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one Sodium azide (1.08 g, 16.62 mmol) was suspended in N,N-dimethylformamide (10 mL) and a stock solution of 3,4-dibromo-1-(3-fluorobenzyl)pyridin-2(1H)-one (from step 1) in N,N-dimethylformamide (33.0 mL, 0.33 M) was added and the resulting mixture was heated to 60° C. for 4 hours. Ice water (30 mL) was added and the aqueous layer was extracted with ethyl acetate (4×50 mL). The combined organics were washed with H₂O (3×50 mL), brine (2×25 mL), dried over MgSO₄, concentrated, and subjected to chromatography (silica gel, ethyl acetate with 10% methanol/hexane) to afford an off-white solid (3.50 g, 98%).

Step 3. Preparation of 4-amino-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one hydrochloride 4-azido-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one (from step 2) (4.00 g, 12.38 mmol) was suspended in ethyl acetate (300 mL) and Fe (2.07 g, 37.14 mmol) was added. A stock solution of NH₄Cl in H₂O (300 mL, 0.2 M) was added and the reaction mixture was stirred at room temperature for 36 hours. The reaction was filtered through a pad of Celite® and concentrated. The resulting solid was dissolved in ethyl acetate (150 mL) and washed with water (3×50 mL), brine (50 mL), dried over MgSO₄, and concentrated. ¹H NMR (400 MHz, CD₃OD) δ 7.38-7.29 (m, 2H), 7.05 (d, J=7.79 Hz, 1H), 6.99 (d, J=8.99 Hz, 2H), 6.03 (d, J=7.39 Hz 1H), 5.09 (s, 2H). ES-HRMS m/z 297.0023 (M+H C₂₀H₁₇BrF₂N₂O₂ requires 297.0033).

Step 4: Preparation of N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-2,6-difluorobenzamide. 4-amino-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one (from step 3) (0.30 g, 1.01 mmol) and 4-dimethylaminopyridine (0.002 g, 0.01 mmol) were suspended in acetonitrile (5 mL) followed by dropwise addition of triethylamine (0.2 mL, 1.41 mmol). This reaction mixture was stirred for 10 minutes at room temperature before being cooled to 0° C. 2,6-difluorobenzoyl chloride (0.37 g, 2.12 mmol) was added dropwise and the reaction was heated at reflux overnight. The reaction was cooled to room temperature and 1N NaOH (10 mL) was added. The reaction was then stirred for 45 minutes at room temperature. The reaction mixture was extracted with ethyl acetate (3×25 mL) and the organic layer washed with 1N NaOH (2×25 mL), H₂O (until pH neutral), brine (50 mL), dried over MgSO₄, concentrated, and subjected to chromatography (on C-18, acetonitrile/H₂O with 0.1% trifluoracetic acid) to afford a white solid (0.19 g, 43%). ¹H NMR (400 MHz, CDCl₃) δ 8.42 (br s, 1H), 7.67 (d, J=7.65 Hz, 1H), 7.49 (app tt, J=6.31, 8.60 Hz, 1H), 7.33-28 (m, 2H), 7.10-6.97 (m, 5H), 5.17 (s, 2H). ES-HRMS m/z 437.0083 (M+H C₁₉H₁₂BrF₃N₂O₂ requires 437.0107).

Example 312

Preparation of 3-bromo-1-(4-bromo-2,6-difluorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 1-(4-bromo-2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one. 4-Hydroxy-6-methyl-2-pyrone (30.0 g, 238 mmol) and 4-bromo-2,6-difluoroaniline (49.5 g, 238 mmol) were suspended in 50 ml of 1,2-dichlorobenzene in a 250 ml, 3-necked, round bottom flask equipped with a J-Kem temperature controller probe, a Dean-Stark trap, and a heating mantle. The reaction was heated to 165° C. for 15 minutes, during which, water and some 1,2-dichlorobenzene was collected in the Dean-Stark trap. The reaction was allowed to cool to about 80° C. The flask was placed in an ice bath and about 25 ml of toluene was added and stirred. After about 10 minutes, a precipitate formed. The precipitate was filtered and washed 3 times with toluene, 3 times with hot water to remove excess pyrone, and dried in vacuo to give a tan solid (22.1 g, 29%). ¹H NMR (400 MHz, DMSO-d₆) δ 11.00 (br s, 1H), 7.71 (d, J=6.98 Hz, 2H), 5.97 (t, J=0.88 Hz, 1H), 5.55 (d, J=2.28 Hz, 1H), 1.91 (s, 3H). LC/MS, t_r=1.96 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS nm/z 316 (M+H). ES-HRMS nz/z 315.9779 (M+H calcd for C₁₂H₈BrF₂NO₂ requires 315.9779).

Step 2: Preparation of 1-(4-bromo-2,6-difluorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one 1-(4-bromo-2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (from Step 1) (5.0 g, 15.8 mmol) was stirred briskly at room temperature with 2,4-difluorobenzyl bromide (2.23 ml, 17.4 mmol) and K₂CO₃ (3.27 g, 23.7 mmol) in 50 ml of dimethylformamide. After stirring overnight, the reaction was poured quickly into 900 ml of cold water. The resulting precipitate was filtered and washed with water and hexane. The product was purified using a Biotage silica chromatography system using 20% ethyl acetate/hexanes to give a beige solid (4.32 g, 62%). ¹H NMR (400 MHz, CDCl₃) δ 7.41 (app q, J=6.31 Hz, 1H), 7.25 (dd, J=8.33, 1.74 Hz, 2H), 6.91 (dt, J=9.2, 0.8 Hz, 1H), 6.86 (dt, J=9.2, 0.8 Hz, 1H), 5.95 (d, J=2.56 Hz, 1H), 5.92 (dd, J=2.56, 0.94 Hz, 1H), 5.01 (s, 2H), 1.98 (s, 3H). LC/MS, t_r=3.04 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 442 (M+H). ES-HRMS m/z 442.0057 (M+H calcd for C₁₉H₁₂BrF₄NO₂ requires 442.0060).

Step 3: Preparation of 3-bromo-1-(4-bromo-2,6-difluorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. 1-(4-bromo-2,6-difluorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (from Step 2) (500 mg, 1.13 mmol) was stirred at room temperature with N-bromosuccinimide (221 mg, 1.24 mmol) in 5 ml of CH₂Cl₂ for 1.5 hours. The reaction was evaporated on a rotary evaporator and the resulting solid was washed 4 times with acetonitrile and dried in vacuo to yield a white solid (478 mg, 92%). ¹H NMR (300 MHz, CDCl₃) δ 7.62 (app q, J=6.64 Hz, 1H), 7.31 (d, J=6.85 Hz, 2H), 7.01 (app t, J=8.36 Hz, 1H), 6.96 (dt, J=9.46, 2.21 Hz, 1H), 6.19 (s, 1H), 5.30 (s, 2H), 2.10 (s, 3H); LC/MS, t_r=3.17 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 520 (M+H). ES-HRMS m/z 521.9134 (M+H calcd for C₁₉H₁₁Br₂F₄NO₂ requires 521.9146).

Example 313

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one

The title compound was produced essentially as in Example 313, using 2,4,6-trifluoroaniline instead of 4-bromo-2,6-difluoroaniline. ¹H NMR (300 MHz, CDCl₃) δ 7.62 (app q, J=7.79 Hz, 1H), 7.01 (app dt, J=8.26, 2.01 Hz, 1H), 6.95-6.85 (m, 3H), 6.19 (s, 1H), 5.30 (s, 2H), 2.11 (s, 3H); LC/MS, t_r=2.81 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 460 (M+H). ES-HRMS m/z 459.9954 (M+H calcd for C₁₉H₁₁BrF₅NO₂ requires 459.9966).

Example 314

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one

4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one (350 mg, 0.92 mmol) was refluxed with N-chlorosuccinimide (147 mg, 1.1 mmol) and dichloroacetic acid (0.038 ml, 0.46 mmol) in 5 ml of CH₂Cl₂ overnight. The reaction was evaporated on a rotary evaporator and the resulting solid was washed 4 times with acetonitrile and dried in vacuo to yield a white solid (217 mg, 57%). ¹H NMR (300 MHz, CDCl₃) δ 7.60 (app q, J=7.75 Hz, 1H), 7.00 (app dt, J=8.23, 2.05 Hz, 1H), 6.93-6.86 (m, 3H), 6.22 (s, 1H), 5.30 (s, 2H), 2.12 (s, 3H); LC/MS, t_r=2.78 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 416 (M+H). ES-HRMS m/z 416.0472 (M+H calcd for C₁₉H₁₁ClF₅NO₂ requires 416.0471).

Example 315

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one

Step 1. Preparation of 4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one 4-[(2,4-Difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one (9.0 g, 23.6 mmol) was heated to 135° C. overnight with SeO₂ (13.1 g, 118 mmol) in 75 ml of 1,4-dioxane in a 350 ml sealed glass pressure vessel. The reaction mixture was cooled and placed on a plug of silica gel and washed with 5% methanol in CH₂Cl₂. The filtrate was evaporated and the resulting solid was washed with diethyl ether and dissolved in hot ethyl acetate. The insoluble Se salts were filtered off and the organic layer was evaporated. 7.01 g (17.6 mmol) of a 3:1 ratio of aldehyde to desired alcohol was isolated. The mixture was stirred with NaBH₄ (802 mg, 21.2 mmol) in 30 ml of methanol at room temperature for 1 hour. The reaction was evaporated and CH₂Cl₂ and acetonitrile were used to dissolve the bulk of the solid. The remaining insoluble solid was filtered off. The organic layer was washed 3 times with NH₄Cl, dried over MgSO₄ and evaporated. The resulting solid was washed 3 times with diethyl ether and dried in vacuo to yield a light orange solid (4.35 g, 46%). ¹NMR (300 MHz, DMSO-d₆) δ 7.68 (app q, J=7.92 Hz, 1H), 7.47 (app t, J=8.57 Hz, 2H), 7.35 (dt, J=9.87, 2.42 Hz, 1H), 7.18 (dt, J=8.31, 1.71 Hz, 1H), 6.21 (d, J=2.42 Hz, 1H), 6.07 (d, J=2.62 Hz, 1H), 5.67 (br s, 1H), 5.18 (s, 2H), 3.98 (s, 2H); LC/MS, t_r=2.31 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 398 (M+H).

Step 2. Preparation of 4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one. 4-[(2,4-Difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one (from step 1) (2.1 g, 5.28 mmol) was stirred at room temperature with N-bromosuccinimide (1.13 g, 6.34 mmol) in 5 ml CH₂Cl₂ for 2 hours. The reaction was evaporated on a rotary evaporator and the resulting solid was washed 4 times with acetonitrile and dried in vacuo to yield a white solid (1.35 g, 54%). ¹NMR (300 MHz, CD₃OD) δ 7.69 (app q, J=6.65 Hz, 1H), 7.20 (app t, J=8.36 Hz, 2H), 7.09 (app t, J=8.46 Hz, 2H), 6.88 (s, 1H), 5.46 (s, 2H), 4.21 (s, 2H); LC/MS, t_r=2.48 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 476 (M+H). ES-HRMS m/z 475.9907 (M+H calcd for C₁₉H₁₁BrF₅NO₃ requires 475.9915).

Example 316

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one

4-[(2,4-Difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one (2.1 g, 5.28 mmol) was refluxed with N-chlorosuccinimide (846 mg, 6.34 mmol) and dichloroacetic acid (0.87 ml, 10.56 mmol) in 5 ml CH₂Cl₂ overnight. The reaction was evaporated on a rotary evaporator and the resulting oil was triturated with diethyl ether to obtain a solid. The solid was washed 4 times with acetonitrile. Chromatography was done using a Biotage silica gel system with 60% ethyl acetate/hexanes. The recovery was poor from the column to give a white solid (109 mg, 5%). ¹NMR (300 MHz, CD₃OD) δ 7.67 (app q, J=7.85 Hz, 1H), 7.24-7.06 (m, 4H), 6.90 (s, 1H), 5.45 (s, 2H), 4.22 (s, 2H); LC/MS, t_r=2.71 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 432 (M+H). ES-HRMS m/z 432.0413 (M+H calcd for C₁₉H₁₁ClF₅NO₃ requires 432.0420).

Example 317

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-morpholin-4-ylphenyl)-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-morpholin-4-ylphenyl)-6-methylpyridin-2(1H)-one. 4-[(2,4-Difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one (870 mg, 2.28 mmol) was heated to 100° C. with K₂CO₃ (630 mg, 4.56 mmol) in 5 ml of morpholine for 36 hours. The reaction was added to 200 ml of cold water and the resulting solid was washed with water and 50:50 diethyl ether/hexanes and dried in vacuo to give a beige solid (738 mg, 72%). ¹NMR (400 MHz, CDCl₃) δ 7.41 (app q, J=7.70 Hz, 1H), 6.93-6.85 (m, 2H), 6.49 (d, J=10.47 Hz, 2H), 5.96 (d, J=2.41 Hz, 1H), 5.89 (d, J=1.75 Hz, 1H), 5.00 (s, 2H), 3.83 (t, J=4.83 Hz, 4H), 3.19 (t, J=4.84 Hz, 4H), 1.99 (s, 3H); LC/MS, t_r=3.09 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 449 (M+H). ES-HR/MS m/z 449.1485 (M+H calcd for C₂₃H₂₀F₄N₂O₃ requires 449.1483).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-morpholin-4-ylphenyl)-6-methylpyridin-2(1H)-one. 4-[(2,4-Difluorobenzyl)oxy]-1-(2,6-difluoro-4-morpholin-4-ylphenyl)-6-methylpyridin-2(1H)-one (from step 1) (500 mg, 1.12 mmol) was stirred at room temperature with N-bromosuccinimide (236 mg, 1.33 mmol) in 5 ml of CH₂Cl₂ for 2 hours. The reaction was evaporated on a rotary evaporator and the resulting oil was triturated with diethyl ether to obtain a solid. The solid was washed 4 times with acetonitrile and dried in vacuo to yield a white solid (171 mg, 29%). ¹NMR (400 MHz, CDCl₃) δ 7.58 (app q, J=7.74 Hz, 1H), 6.96 (app t, J=8.39 Hz, 1H), 6.86 (dt, J=9.46, 2.28 Hz, 1H), 6.50 (d, J=10.74 Hz, 2H), 6.09 (s, 1H), 5.24 (s, 2H), 3.84 (t, J=4.84 Hz, 4H), 3.20 (t, J=4.83 Hz, 4H), 2.07 (s, 3H); LC/MS, t_r=3.18 minutes (5 to 95% acetonitrile/water over 5 minutes at mil/min, at 254 nm, at 50° C.), ES-MS m/z 527 (M+H). ES-HRMS m/z 527.0570 (M+H calcd for C₂₃H₁₉BrF₄N₂O₃ requires 527.0588).

Example 318

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(4-methylpiperazin-1-yl)phenyl]-6-methylpyridin-2(1H)-one

The title compound was prepared essentially as in Example 317, using 1-methylpiperazine instead of morpholine. ¹H NMR (400 MHz, CDCl₃) δ 7.57 (app q, J=7.79 Hz, 1H), 6.96 (dt, J=8.19, 1.88 Hz, 1H), 6.86 (app dt, J=9.44, 2.48 Hz, 1H), 6.52 (d, J=10.61 Hz, 2H), 6.14 (s, 1H), 5.24 (s, 2H), 3.72 (br s, 4H), 3.51 (d, J=11.27 Hz, 2H), 3.07 (br s, 2H), 2.85 (d, J=4.29 Hz, 3H), 2.06 (s, 3H); LC/MS, t_r=2.50 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 540 (M+H). ES-HRMS m/z 540.0930 (M+H calcd for C₂₄H₂₂BrF₄N₃O₂ requires 540.0904).

Example 320

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(4-methylpiperazin-1-yl)phenyl]-6-methylpyridin-2(1H)-one

4-[(2,4-Difluorobenzyl)oxy]-1-[2,6-difluoro-4-(4-methylpiperazin-1-yl)phenyl]-6-methylpyridin-2(1H)-one (1.3 g, 2.82 mmol) was stirred at reflux with N-chlorosuccinimide (451 mg, 3.38 mmol) and dichloroacetic acid (0.17 ml, 1.41 mmol) in 6 ml CH₂Cl₂ overnight. LC-MS showed 33% completion. More N-chlorosuccinimide (271 mg, 2.23 mmol) was added and refluxed overnight. The reaction was evaporated on a rotary evaporator and the resulting oil was triturated with ethyl acetate to obtain a solid. The solid was washed 4 times with ethyl acetate and with diethyl ether and dried in vacuo to obtain a white solid (606 mg, 43%). ¹NMR (400 MHz, DMSO-d₆) δ 7.66 (br q, J=7.74 Hz, 1H), 7.33 (br t, J=9.00 Hz, 1H), 7.16 (br t, J=7.65 Hz, 1H), 6.96 (d, J=11.81 Hz, 2H), 6.79 (s, 1H), 5.33 (s, 2H), 3.61 (br m, 4H), 3.25 (br m, 4H), 3.21 (br s, 3H), 2.04 (s, 3H); LC/MS, t_r=2.45 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 496 (M+H). ES-HRMS m/z 496.1400 (M+H calcd for C₂₄H₂₂ClF₄N₃O₂ requires 496.1409).

Example 321

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(dimethylamino)-2,6-difluorophenyl]-6-methylpyridin-2(1H)-one

The title compound was prepared essentially as described in Example 317, using dimethylamine instead of morpholine. ¹NMR (400 MHz, CDCl₃) δ 7.59 (q, J=7.74 Hz, 1H), 6.95 (dt, J=8.32, 1.61 Hz, 1H), 6.85 (app dt, J=9.54, 2.41 Hz, 1H), 6.27 (d, J=11.01 Hz, 2H), 6.08 (s, 1H), 5.23 (s, 2H), 2.98 (s, 3H), 2.07 (s, 3H); LC/MS, t_r=3.35 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 485 (M+H). ES-HRMS m/z 485.0447 (M+H calcd for C₂₁H₁₇BrF₄N₂O₂ requires 485.0482).

Example 322

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(2-hydroxyethyl)(methyl)amino]phenyl}-6-methylpyridin-2(1H)-one

The title compound was prepared essentially as in Example 317, using 2-(methylamino)ethanol instead of morpholine. ¹NMR (400 MHz, CDCl₃) δ 7.58 (q, J=7.74 Hz, 1H), 6.95 (dt, J=8.24, 1.66 Hz, 1H), 6.85 (app dt, J=9.49, 2.37 Hz, 1H), 6.35 (d, J=11.01 Hz, 2H), 6.10 (s, 1H), 5.23 (s, 2H), 3.77 (t, J=5.77 Hz, 2H), 3.45 (t, J=5.78 Hz, 2H), 2.99 (s, 3H), 2.08 (s, 3H); LC/MS, t_r=2.96 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 515 (M+H). ES-HRMS m/z 515.0576 (M+H calcd for C₂₂H₁₉BrF₄N₂O₃ requires 515.0588).

Example 323

Preparation of 3-bromo-1-(3,5-dibromo-2,6-difluoro-4-hydroxyphenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-hydroxyphenyl)-6-methylpyridin-2(1H)-one. 4-[(2,4-Difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one (step 2 above) (10.0 g, 26.2 mmol) was heated to 45° C. with KOSiMe₃ (10.08 g, 78.6 mmol) in 50 ml of tetrahydrofuran for 4 days. The reaction was diluted with 30 ml of ethyl acetate and washed with 1N HCl and water, dried over MgSO₄, and evaporated to give an orange solid. The solid was stirred in hot 60% ethyl acetate/hexanes and filtered to give a white solid, which was dried in vacuo to obtain a white solid (3.79 g, 38%). The filtrate was found to contain a mixture of desired product and the ortho substituted regioisomer. ¹NMR (400 MHz, CDCl₃) δ 7.42 (app q, J=7.70 Hz, 1H), 6.95-6.83 (m, 2H), 6.34 (d, J=9.40 Hz, 2H), 6.05 (app s, 2H), 5.06 (s, 2H), 2.01 (s, 3H); LC/MS, t_r=2.80 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 380 (M+H). ES-HRMS m/z 380.0926 (M+H calcd for C₁₉H₁₃F₄NO₃ requires 380.0904).

Step 2. Preparation of 3-bromo-1-(3,5-dibromo-2,6-difluoro-4-hydroxyphenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. 4-[(2,4-Difluorobenzyl)oxy]-1-(2,6-difluoro-4-hydroxyphenyl)-6-methylpyridin-2(1H)-one (from step 1) (3.73 g, 8.14 mmol) was stirred as a suspension at room temperature with N-bromosuccinimide (1.52 g, 8.55 mmol) in 30 ml CH₂Cl₂ overnight. LC-MS showed a 60% starting material. The solid was filtered off, dissolved in 30 ml of CH₂Cl₂/N,N-dimethylformamide and stirred with more N-bromosuccinimide (0.76 g, 4.28 mmol) overnight. LC-MS showed the tri-brominated product as the major product. The reaction was poured into water and extracted with n-butanol. The combined organic layers were evaporated on a rotary evaporator and the resulting solid was washed with diethyl ether and dried in vacuo to yield a white solid (873 mg, 17%). ¹NMR (400 MHz, CDCl₃) δ 7.67 (app q, J=7.80 Hz, 1H), 7.32 (dt, J=4.86, 2.11 Hz, 1H), 7.16 (dt, J=8.48, 1.84 Hz, 1H), 6.79 (s, 1H), 5.35 (s, 2H), 2.08 (s, 3H); LC/MS, t_r=3.26 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 616 (M+H). ES-HRMS m/z 615.8234 (M+H calcd for C₁₉H₁₀Br₃F₄NO₃ requires 615.8200).

Example 324

Preparation of 2-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenoxy}acetamide

Step 1: Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-hydroxyphenyl)-6-methylpyridin-2(1H)-one 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2,4,6-trifluorophenyl)pyridin-2(1H)-one (7.5 g, 16.3 mmol) was heated to 45° C. with KOSiMe₃ (10.08 g, 78.6 mmol) in 50 ml of tetrahydrofuran for 48 hours. The reaction was diluted with 30 ml of ethyl acetate and washed with 1N HCl and water, dried over MgSO₄, and evaporated to give a black oil. The oil was dissolved in ethyl acetate. A precipitate formed upon standing, which was filtered, washed with ethyl acetate and dried in vacuo to obtain a white solid (2.80 g, 37%). The filtrate showed the presence of desired product and the ortho substituted regioisomer. ¹NMR (400 MHz, DMSO-d₆) δ 7.66 (q, J=7.92 Hz, 1H), 7.32 (dt, J=8.77, 2.19 Hz, 1H), 7.15 (m, 1H), 6.73 (s, 1H), 6.67 (d, J=9.66 Hz, 2H), 5.33 (s, 2H), 2.03 (s, 3H); LC/MS, t_r=2.92 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 458 (M+H). ES-HRMS m/z 457.9995 (M+H calcd for C₁₉H₁₂BrF₄NO₃ requires 458.0009).

Step 2. Preparation of 2-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenoxy}acetamide. 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-hydroxyphenyl)-6-methylpyridin-2(1H)-one (from step 1) (500 mg, 1.09 mmol) was stirred briskly with 2-bromoacetamide (196 mg, 1.43 mmol) and K₂CO₃ (282 mg, 2.05 mmol) in 5 ml of N,N-dimethylformamide at room temperature for 24 hours. The reaction was poured quickly into cold water and the resulting solid was filtered, washed with water, acetonitrile, and diethyl ether, and dried in vacuo to give a white solid (289 mg, 51%). ¹NMR (400 MHz, DMSO-d₆) δ 7.66 (q, J=7.92 Hz, 1H), 7.61 (br s, 1H), 7.45 (br s, 1H), 7.33 (dt, J=10.07, 2.15 Hz, 1H), 7.16 (dt, J=8.53, 1.88 Hz, 1H), 6.99 (d, J=9.54 Hz, 2H), 6.76 (s, 1H), 5.34 (s, 2H), 2.03 (s, 3H); LC/MS, t_r=2.70 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 515 (M+H). ES-HRMS m/z 515.0245 (M+H calcd for C₂₁H₁₅BrF₄N₂O₄ requires 515.0224).

Example 325

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(2-hydroxyethoxy)phenyl]-6-methylpyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described for Example 324. ¹NMR (400 MHz, DMSO-d₆) δ 7.66 (q, J=7.92 Hz, 1H), 7.33 (dt, J=10.04, 2.19 Hz, 1H), 7.17 (dt, J=8.68, 1.84 Hz, 1H), 6.99 (d, J=9.67 Hz, 2H), 6.75 (s, 1H), 5.34 (s, 2H), 4.92 (t, J=4.86 Hz, 1H), 4.07 (t, J=4.77 Hz, 2H), 3.70 (t, J=4.83 Hz, 2H), 2.03 (s, 3H); LC/MS, t_r=2.81 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 502 (M+H). ES-HRMS m/z 502.0291 (M+H calcd for C₂₁H₁₆BrF₄NO₄ requires 502.0272).

Example 326

Preparation of 3-bromo-1-(2,6-difluorophenyl)-4-{[4-fluoro-2-(hydroxymethyl)benzyl]oxy}-6-methylpyridin-2(1H)-one

Step 1: Preparation of 1-(2,6-difluorophenyl)-4-{[4-fluoro-2-(hydroxymethyl)benzyl]oxy}-6-methylpyridin-2(1H)-one. 1-(2,6-Difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (step 1) (3.0 g, 12.65 mmol) was dissolved in N,N-dimethylformamide and cooled to 0° C. Triphenylphosphine (3.98 g, 15.18 mmol) and diethyl azodicarboxylate (2.39 ml, 15.18 mmol) were added and stirred for 10 minutes. 1,2-Bis(hydroxymethyl)-4-fluorobenzene (2.57 g, 16.44 mmol) was added and stirred at 0° C. for 1 hour, then allowed to warm to room temperature and stirred overnight. LC-MS showed only 1 product, not a mixture of regioisomers, as expected. The reaction was added to water and extracted 3 times with ethyl acetate. The combined organic layers were dried over MgSO₄ and evaporated. A Biotage silica column was done using 60% ethyl acetate/hexanes as an eluent. Desired product, with a substantial impurity was obtained. Another Biotage silica column was ran using 30% ethyl acetate/hexanes to obtain pure product. The resulting oil was triturated with diethyl ether to obtain a white solid (720 mg, 15%). ¹NMR (300 MHz, CDCl₃) δ 7.51-7.39 (m, 2H), 7.26 (dd, J=9.62, 2.51 Hz, 1H), 7.13-7.01 (m, 3H), 6.03 (d, J=2.42 Hz, 1H), 5.96 (d, J=2.41 Hz, 1H), 5.06 (s, 2H), 4.73 (s, 2H), 2.81 (br s, 1H), 2.02 (s, 3H); LC/MS, t_r=2.37 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 376 (M+H). ES-HR/MS m/z 376.1181 (M+H calcd for C₂₀H₁₆F₃NO₃ requires 376.1155). Identity of the positional isomer was determined from hmbc, 2-D NMR experiments using H to C 2- and 3-bond coupling.

Step 2: Preparation of 3-bromo-1-(2,6-difluorophenyl)-4-{[4-fluoro-2-(hydroxymethyl)benzyl]oxy}-6-methylpyridin-2(1H)-one. 1-(2,6-Difluorophenyl)-4-{[4-fluoro-2-(hydroxymethyl)benzyl]oxy}-6-methylpyridin-2(1H)-one (from step 1) (350 mg, 0.93 mmol) was stirred at room temperature with N-bromosuccinimide (199 mg, 1.12 mmol) in 1.5 ml CH₂Cl₂ for 1.5 hours. The reaction was evaporated on a rotary evaporator and the resulting solid was washed 4 times with acetonitrile and dried in vacuo to yield a white solid (197 mg, 47%). ¹NMR (300 MHz, CDCl₃) δ 7.53-7.43 (m, 2H), 7.25 (dd, J=9.46, 2.62 Hz, 1H), 7.11-7.03 (m, 3H), 6.25 (s, 1H), 5.31 (s, 2H), 4.81 (s, 2H), 2.28 (br s, 1H), 2.10 (s, 3H); LC/MS, t_r=2.38 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 454 (M+H). ES-HRMS m/z 454.0247 (M+H calcd for C₂₀H₁₅BrF₃NO₃ requires 454.0260).

Example 327

Preparation of 3-chloro-1-(2,6-difluorophenyl)-4-{[4-fluoro-2-(hydroxymethyl)benzyl]oxy}-6-methylpyridin-2(1H)-one

1-(2,6-Difluorophenyl)-4-[4-fluoro-2-(hydroxymethyl)benzyl]oxy}-6-methylpyridin-2(1H)-one (step 1 above) (275 mg, 0.73 mmol) was stirred at reflux with N-chlorosuccinimide (117 mg, 0.88 mmol) and dichloroacetic acid (0.03 ml, 0.36 mmol) in 1.5 ml CH₂Cl₂ overnight. The reaction was evaporated on a rotary evaporator and the resulting solid was washed 4 times with ethyl acetate and with diethyl ether and dried in vacuo to obtain a white solid (65.5 mg, 22%). ¹H NMR (300 MHz, CDCl₃) δ 7.52-7.43 (m, 2H), 7.26 (dd, J=9.38, 2.52 Hz, 1H), 7.12-7.04 (m, 3H), 6.27 (s, 1H), 5.32 (s, 2H), 4.82 (s, 2H), 2.29 (br s, 1H), 2.11 (s, 3H); LC/MS, t_r=2.32 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 410 (M+H). ES-HRMS m/z 410.0755 (M+H calcd for C₂₀H₁₅ClF₃NO₃ requires 410.0765).

Example 328

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methyl-N-(2-morpholin-4-ylethyl)benzamide

Step 1: Preparation of methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-2-methylbenzoate. 4-Hydroxy-6-methyl-2-pyrone (72.6 g, 576 mmol) and methyl-3-amino-2-methylbenzoate (100 g, 605 mmol) were suspended in 75 ml of 1,2-dichlorobenzene in a 500 ml, 3-necked round bottom flask equipped with a J-Kem temperature controller probe, a Dean-Stark trap, and a heating mantle. The reaction was heated to 165° C. for 15 minutes, during which, water and some 1,2-dichlorobenzene was collected in the Dean-Stark trap. The reaction was allowed to cool to about 80° C. The flask was placed in an ice bath and about 300 ml of toluene was added and stirred. After about 30 minutes, a precipitate formed. The precipitate was filtered and washed 3 times with toluene, 3 times with hot water to remove excess pyrone, and dried in vacuo to give a tan solid (44.6 g, 28% yield). ¹H NMR (400 MHz, DMSO-d₆) δ 10.66 (br s, 1H), 7.80 (dd, J=7.72, 1.28 Hz, 1H), 7.33 (dd, J=7.78, 1.34 Hz, 1H), 5.91 (dd, J=2.41, 0.69 Hz, 1H), 5.55 (d, J=2.42 Hz, 1H), 3.82 (s, 3H), 2.06 (s, 3H), 1.73 (s, 3H); LC/MS, t_r=1.85 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 274 (M+H). ES-HRMS m/z 274.1078 (M+H calcd for C₁₅H₁₅NO₄ requires 274.1074).

Step 2: Preparation of methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoate. Methyl-3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-2-methylbenzoate (from Step 1) (42.0 g, 154 mmol) was stirred briskly at room temperature with 2,4-difluorobenzyl bromide (19.7 ml, 154 mmol) and K₂CO₃ (31.8 g, 231 mmol) in 250 ml of N,N-dimethylformamide. After stirring overnight, the reaction was poured into 1 L of cold water. The solution was extracted 3 times with ethyl acetate and the organic layers were dried over MgSO₄, and evaporated. The product was carried on to the next step as a crude oil (60.4 g, 85%). ¹NMR (400 MHz, CDCl₃) δ 7.96 (dd, J=7.85, 1.28 Hz, 1H), 7.45-7.34 (m, 2H), 7.27-7.23 (m, 1H), 6.94-6.84 (m, 2H), 5.98 (d, J=2.68 Hz, 1H), 5.92 (dd, J=2.69, 0.81 Hz, 1H), 5.01 (s, 2H), 3.88 (s, 3H), 2.28 (s, 3H), 1.81 (s, 3H); LC/MS, t_r=2.96 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 400 (M+H). ES-HRMS m/z 400.1341 (M+H calcd for C₂₂H₁₉F₂NO₄ requires 400.1355).

Step 3. Preparation of 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid. Methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoate (from Step 2) (60.0 mg, 150 mmol) was stirred with 2.5 N NaOH (120 ml, 300 mmol) in 375 ml of tetrahydrofuran and 75 ml of water at room temperature overnight. The reaction was acidified with 1 N HCl, 350 ml of water was added and the solution was extracted 3 times with ethyl acetate. The combined organic layers were dried over MgSO₄, filtered and evaporated. The resulting solid was filtered, washed with ethyl acetate and dried in vacuo to yield a white solid 33.8 g, 58%). ¹NMR (400 MHz, CDCl₃) δ 7.98 (dd, J=7.92, 1.20 Hz, 1H), 7.43 (app q, J=7.70 Hz, 1H), 7.38 (t, J=7.72 Hz, 1H), 7.35 (dd, J=7.81, 1.21 Hz, 1H), 6.92-6.84 (m, 2H), 6.17 (d, J=2.56 Hz, 1H), 6.00 (dd, J=2.55, 0.81 Hz, 1H), 5.05 (s, 2H), 2.30 (s, 3H), 1.84 (s, 3H); LC/MS, t_r=2.61 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS nm/z 386 (M+H). ES-HR/MS m/z 386.1228 (M+H calcd for C₂₁H₁₇F₂NO₄ requires 386.1198).

Step 4: Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid. 3-[4-[(2,4-Difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid (from Step 3) (23.0 g, 59.7 mmol) was stirred at room temperature with N-bromosuccinimide (12.74 g, 71.6 mmol) in 120 ml of CH₂Cl₂ for 2 hours. The reaction was evaporated on a rotary evaporator and the resulting solid was stirred in acetonitrile for 1 hour, washed 7 times with acetonitrile and dried in vacuo to yield a white solid (19.14 g, 69%). ¹NMR (400 MHz, DMSO-d₆) δ 7.87 (dd, J=7.52, 1.61 Hz, 1H), 7.67 (app q, J=7.92 Hz, 1H), 7.45-7.37 (m, 2H), 7.33 (dt, J=9.87, 2.54 Hz, 1H), 7.17 (dt, J=8.50, 1.67 Hz, 1H), 6.71 (s, 1H), 5.32 (s, 2H), 2.08 (s, 3H), 1.86 (s, 3H); LC/MS, t_r=2.69 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 464 (M+H). ES-HRMS m/z 464.0284 (M+H calcd for C₂₁H₁₆BrF₂NO₄ requires 464.0304).

Step 5: Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methyl-N-(2-morpholin-4-ylethyl)benzamide. 3-[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid (from Step 4 above) (500 mg, 1.08 mmol) was dissolved in 5 ml of CH₂Cl₂. 4-(2-Aminoethyl)morpholine (170 μl, 1.29 mmol) was added, followed, in order, by EDCI (247 mg, 1.29 mmol), 1-hydroxybenzotriazole (174 mg, 1.29 mmol) and triethylamine (301 μl, 2.16 mmol). The reaction was stirred at room temperature overnight. The reaction was quenched with NH₄Cl and extracted 3 times with ethyl acetate. The combined organic layer was dried over MgSO₄ and evaporated. The resulting oil was triturated with diethyl ether/hexane to obtain a solid, which was dried in vacuo to give a white solid (472 mg, 76%). ¹NMR (400 MHz, DMSO-d₆) δ 7.64 (app q, J=7.79 Hz, 1H), 7.47 (dd, J=7.65, 1.01 Hz, 1H), 7.39 (t, J=7.75 Hz, 1H), 7.17 (dd, J=7.65, 0.81 Hz, 1H), 7.01 (dt, J=8.26, 1.61 Hz, 1H), 6.91 (dt, J=9.42, 2.32 Hz, 1H), 6.49 (t, J=5.04 Hz, 1H), 6.18 (s, 1H), 5.30 (s, 2H), 3.73 (t, J=4.53 Hz, 4H), 3.68-3.47 (m, 2H), 2.59 (t, J=5.94 Hz, 2H), 2.51 (t, J=4.33 Hz, 4H), 2.15 (s, 3H), 1.98 (s, 3H); LC/MS, t_r=2.27 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS nz/z 576 (M+H). ES-HRMS m/z 576.1313 (M+H calcd for C₂₇H₂₈BrF₂N₃O₄ requires 576.1304).

Examples 329-337

Preparation of Compounds Corresponding in Structure to the Following Formula

The following compounds are prepared essentially according to the procedure set forth for Example 328:

			M + H	ESHRMS
Example No.	R	MF	Requires	m/z
Ex. 329	—NHCH2CH2OCH3	C24H22BrF2N2O4	521.0882	521.0906
Ex. 330	—N(CH3)2	C23H20BrF2N2O3	491.0776	491.0752
Ex. 331	—NHCH2CH2OH	C23H20BrF2N2O4	507.0726	507.0689
Ex. 332	—NHCH3	C22H18BrF2N2O3	477.0620	477.0585
Ex. 333	—N(CH3)CH2CH2OH	C24H22BrF2N2O4	521.0882	521.0890
Ex. 334	4-methylpiperazin-1-yl	C26H25BrF2N3O3	546.1198	546.1187
Ex. 335	morpholin-4-yl	C25H22BrF2N2O4	533.0882	533.0856
Ex. 336	—N(CH3)CH2CH2OCH3	C25H24BrF2N2O4	535.1039	535.1055
Ex. 337	—NH2	C21H16BrF2N2O3	463.0463	463.0492

NMR characterization of compounds of Examples 329-337

Example
No.     NMR Data
Ex. 329 1H NMR (400MHz, CDCl3) δ 7.59(app q, J=7.79Hz, 1H), 7.47(dd, J=7.65, 1.08Hz,
        1H), 7.34(t, J=7.72Hz, 1H), 7.12(dd, J=7.78, 0.94Hz, 1H), 6.96(app dt, J=7.92, 2.27Hz,
        1H), 6.87(dt, J=9.46, 2.55Hz, 1H), 6.29(m, 1H), 6.12(s, 1H), 5.25(s, 2H), 3.73-
        3.65(m, 1H), 3.56-3.48(m, 3H), 3.35(d, J=3.09Hz, 3H), 2.09(s, 3H), 1.93(s, 3H)
Ex. 330 1H NMR (400MHz, CDCl3) δ 7.59(app q, J=7.79Hz, 1H), 7.34(t, J=7.66Hz,
        1H), 7.28(dd, J=7.66, 1.21Hz, 1H), 7.07(dd, J=7.65, 1.08Hz, 1H), 6.96(app
        dt, J=8.52, 2.02Hz, 1H), 6.87(dt, J=9.46, 2.55Hz, 1H), 6.29(m, 1H), 6.12(s,
        1H), 5.25(s, 2H), 3.11(s, 3H), 2.82(s, 3H), 1.96(s, 3H), 1.95(s, 3H)
Ex. 331 1H NMR (400MHz, CDCl3) δ 7.59(app q, J=7.74Hz, 1H), 7.46(d, J=6.71Hz, 1H),
        7.32(t, J=7.72Hz, 1H), 7.07(d, J=6.85Hz, 1H), 6.98(m, 2H), 6.87(dt, J=9.47, 2.41Hz,
        1H), 6.15(s, 1H), 5.26(s, 2H), 3.71(t, J=4.97Hz, 2H), 3.60-3.45(m, 2H), 2.06(s,
        3H), 1.95(s, 3H)
Ex. 332 1H NMR (400MHz, CDCl3) δ 7.59(app q, J=7.79Hz, 1H), 7.42(dd, J=7.66, 0.94Hz,
        1H), 7.31(t, J=7.72Hz, 1H), 7.09(dd, J=7.79, 0.94Hz, 1H), 6.96(app dt, J=8.26, 1.61
        Hz, 1H), 6.87(dt, J=9.44, 2.49Hz, 1H), 6.12(s, 1H), 5.25(s, 2H), 2.96(d, J=4.83Hz,
        3H), 2.07(s, 3H), 1.93(s, 3H)
Ex. 333 1H NMR (300MHz, DMSO-d6) δ 7.73(q, J=7.92Hz, 1H), 7.44-7.20(m, 5H), 6.75(s,
        1H), 5.37(s, 2H), 4.83(br s, 1H), 3.65(br s, 2H), 3.45-3.33(m, 2H), 2.81(s, 3H), 1.93
        (d, J=3.42Hz, 3H), 1.85(d, J=8.06Hz, 3H)
Ex. 334 1H NMR (300MHz, DMSO-d6) δ 7.67(app q, J=7.92Hz, 1H), 7.40(t, J=7.78Hz, 1H),
        7.34(dt, J=9.87, 2.55Hz, 1H), 7.27(d, J=7.52Hz, 1H), 7.24(d, J=7.79Hz, 1H), 7.17
        (dt, J=8.41, 1.97Hz, 1H), 6.71(s, 1H), 5.32(s, 2H), 3.63(m, 2H), 3.29(br s, 1H), 3.09
        (br s, 2H), 2.34(t, J=4.57Hz, 2H), 2.20(br s, 2H), 2.16(s, 3H), 1.88(d, J=8.86Hz, 3H),
        1.80(d, J=4.83Hz, 3H)
Ex. 335 1H NMR (300MHz, CDCl3) δ 7.64(app q, J=7.79Hz, 1H), 7.42(t, J=7.65Hz, 1H),
        7.33(d, J=7.66Hz, 1H), 7.14(d, J=7.65Hz, 1H), 7.00(dt, J=8.76, 2.21Hz, 1H), 6.91
        (dt, J=9.47, 2.42Hz, 1H), 6.17(s, 1H), 5.29(s, 2H), 3.98-3.92(m, 1H), 3.80-3.77(m,
        3H), 3.59(br s, 2H), 3.29(t, J=4.43Hz, 2H), 2.04(s, 3H), 2.00(s, 3H)
Ex. 336 1H NMR (300MHz, CDCl3) δ 7.65(app q, J=7.79Hz, 1H), 7.43-7.32(m, 2H), 7.12
        (dd, J=7.66, 1.21Hz, 1H), 7.00(dt, J=9.06, 1.51Hz, 1H), 6.92(dt, J=9.42, 2.52 Hz,
        1H), 6.16(s, 1H), 5.30(s, 2H), 3.69(t, J=5.04Hz, 2H), 3.39(s, 3H), 3.26(s, 1H), 3.19(s,
        1H), 2.91(s, 3H), 2.04(s, 3H), 2.00(s, 3H)
Ex. 337 1H NMR (300MHz, DMSO-d6) δ 7.91(br s, 1H), 7.73(app q, J=7.85Hz, 1H), 7.53-
        7.20(m, 5H), 6.74(s, 1H), 5.37(s, 2H), 1.99(s, 3H), 1.92(s, 3H)

Example 338

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[3-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

3-[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid (Step 4 above) (2.0 g, 4.31 mmol) was cooled to 0° C. in 10 ml of tetrahydrofuran. 19.5 ml of 1M BH₃ THF in tetrahydrofuran was added and stirred overnight, allowing the temperature to rise to room temperature. The reaction was cooled back down to 0° C. and ice chips were added to quench the reaction. The slurry was extracted 3 times with an ethyl acetate/tetrahydrofuran mixture. The combined organic layers were washed with brine, dried over MgSO₄, filtered and evaporated to give a white solid (1.73 g, 89%). ¹NMR (400 MHz, DMSO-d₆) δ 7.67 (app q, J=7.92 Hz, 1H), 7.46 (d, J=7.52 Hz, 1H), 7.32 (dt, J=10.74, 2.42 Hz, 1H), 7.30 (t, J=7.72 Hz, 1H), 7.17 (dt, J=8.46, 1.88 Hz, 1H), 7.03 (d, J=7.38 Hz, 1H), 6.68 (s, 1H), 5.32 (s, 2H), 4.51 (s, 2H), 3.29 (d, J=9.40 Hz, 1H), 1.85 (s, 3H), 1.81 (s, 3H), LC/MS, t_r=2.64 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 450 (M+H). ES-HRMS m/z 450.0480 (M+H calcd for C₂₁H₁₈BrF₂NO₃ requires 450.0511).

Example 339

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-methoxyethyl)-2-methylbenzamide

Step 1. Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid. 3-[4-[(2,4-Difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid (Step 3 above) (10.0 g, 25.9 mmol) was refluxed with N-chlorosuccinimide (4.15 g, 31.1 mmol) and dichloroacetic acid (1.06 ml, 12.9 mmol) in 50 ml of CH₂Cl₂ overnight. The reaction was evaporated on a rotary evaporator and the resulting solid was stirred in acetonitrile for 30 minutes, washed 4 times with acetonitrile and dried in vacuo to yield a white solid (8.3 g, 78%). ¹H NMR (300 MHz, DMSO-d₆) δ 7.93 (dd, J=7.15, 1.92 Hz, 1H), 7.72 (app q, J=7.92 Hz, 1H), 7.52-7.35 (m, 3H), 7.22 (dt, J=8.47, 2.01 Hz, 1H), 6.80 (s, 1H), 5.38 (s, 2H), 2.14 (s, 3H), 1.93 (s, 3H); LC/MS, t_r=2.64 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 420 (M+H). ES-HRMS m/z 420.0806 (M+H calcd for C₂₁H₁₆ClF₂NO₄ requires 420.0809).

Step 5. Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-methoxyethyl)-2-methylbenzamide. 3-[3-Chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid (from Step 1 above) (500 mg, 1.19 mmol) was dissolved in 5 ml of CH₂Cl₂. 2-Methoxyethylamine (129 μl, 1.49 mmol) was added, followed, in order, by EDCI (286 mg, 1.49 mmol), 1-hydroxybenzotriazole (202 mg, 1.49 mmol) and triethylamine (332 μl, 2.38 mmol). The reaction was stirred at room temperature overnight. The reaction was quenched with NH₄Cl and extracted 3 times with ethyl acetate. The combined organic layer was dried over MgSO₄ and evaporated. The resulting solid was dried in vacuo to give a white solid (401 mg, 71%). ¹H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=7.74 Hz, 1H), 7.47 (d, J=6.98 Hz, 1H), 7.34 (t, J=7.72 Hz, 1H), 7.11 (d, J=7.25 Hz, 1H), 6.95 (dt, J=8.23, 1.66 Hz, 1H), 6.87 (dt, J=9.51, 2.46 Hz, 1H), 6.35 (br s, 1H), 6.15 (s, 1H), 5.25 (s, 2H), 3.72-3.63 (m, 1H), 3.58-3.49 (m, 3H), 3.35 (s, 3H), 2.09 (s, 3H), 1.93 (s, 3H); LC/MS, t_r=2.56 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 477 (M+H). ES-HRMS m/z 477.1363 (M+H calcd for C₂₄H₂₃ClF₂N₂O₄ requires 477.1387).

Example 340

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-m

The title compound was prepared by a procedure similar to the one described for Example 337, where methylamine was used as the amine and the product was obtained in 73% yield. ¹H NMR (300 MHz, DMSO-d₆) δ 8.37 (app d, J=4.64 Hz, 1H), 7.72 (app q, J=7.92 Hz, 1H), 7.44-7.35 (m, 4H), 7.22 (dt, J=8.54, 1.61 Hz, 1H), 6.78 (s, 1H), 5.37 (s, 2H), 2.79 (d, J=4.43 Hz, 3H), 1.95 (s, 3H), 1.94 (s, 3H); LC/MS, t_r=2.46 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 433 (M+H). ES-HRMS m/z 433.1163 (M+H calcd for C₂₂H₁₉ClF₂N₂O₃ requires 433.1125).

Example 341

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-2-methylbenzamide

The title compound was prepared by a procedure similar to the one described above, where ethanolamine was used as the amine and the product was obtained in 65% yield. ¹H NMR (400 MHz, DMSO-d₆) δ 8.39 (t, J=5.51 Hz, 1H), 7.67 (app q, J=7.88 Hz, 1H), 7.43-7.33 (m, 3H), 7.23 (d, J=7.25 Hz, 1H), 7.17 (dt, J=8.39, 1.66 Hz, 1H), 6.74 (s, 1H), 5.32 (s, 2H), 3.48 (br s, 2H), 3.31-3.26 (m, 2H), 1.90 (s, 3H), 1.89 (s, 3H); LC/MS, t_r=2.34 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 463 (M+H). ES-HRMS m/z 463.1220 (M+H calcd for C₂₃H₂₁ClF₂N₂O₄ requires 463.1231).

Example 342

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzamide

3-[3-Chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-methylbenzoic acid (Step 1 above) (500 mg, 1.19 mmol) was stirred with 2-chloro-4,6-dimethoxy-1,3,5-triazine (251 mg, 1.43 mmol) and N-methylmorpholine (392 μl, 3.57 mmol) in 5 ml of tetrahydrofuran at room temperature for 2 hours. 2.5 ml of NH₄OH was added and stirred at room temperature for 2.5 hours. The reaction was diluted with tetrahydrofuran and ethyl acetate and extracted. The combined organic layers were washed with NaHCO₃, 1 N HCl, and brine, dried over MgSO₄, filtered and evaporated. The resulting solid was dried in vacuo to obtain a white solid (313 mg, 63%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.87 (br s, 1H), 7.66 (q, J=7.83 Hz, 1H), 7.48-7.30 (m, 3H), 7.23 (d, J=7.52 Hz, 1H), 7.17 (t, J=7.65 Hz, 1H), 6.73 (s, 1H), 5.32 (s, 2H), 1.94 (s, 3H), 1.88 (s, 3H); LC/MS, t_r=2.44 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 419 (M+H). ES-HRMS m/z 419.0963 (M+H calcd for C₂₁H₁₇ClF₂N₂O₃ requires 419.0969).

Example 343

Preparation of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzonitrile

Step 1: Preparation of 4-[(2,4-difluorobenzyl)oxy]pyridine 1-oxide. 2, 4-Difluorobenzyl alcohol (100. g, 0.694 mol) and 4-nitropyridine N-oxide (98. g, 0.700 mol) are combined with 250 g Cs₂CO₃ (1.1 eq) in 2.5 L anhydrous dimethylformamide and heated to 80° C. with stirring. The reaction was followed by ¹⁹F-NMR (crude reaction mixture with external D₂O reference) and complete after 40 h. The mixture was filtered hot; product crystallized out on cooling. 90.21 g (55%) of white plates were collected by filtration and washed with diethyl ether. The mother liquor was diluted with 2.5 L diethyl ether and stored in the freezer overnight, yielding a second crop 68.76 g (41%, combined yield 96%). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.06 (m, 2H), 7.61 (quartet, J=8.45 Hz, 1H), 7.30 (t, J=10.37 Hz, 1H), 7.12, (t, J=8.45 Hz, 1H), 7.09 (d, J=5.06 Hz, 2H), 5.14 (s, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.43 (quintet, J=7.78 Hz, 1F), −113.82 (quartet, J=9.55 Hz, 1F). LC/MS t_r=3.90 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 238 (M+H).

Step 2. Preparation of 4-[(2,4-difluorobenzyl)oxy]-pyridin-2(1H)-one. 4-[(2,4-difluorobenzyl)oxy]pyridine 1-oxide (from Step 1) (30.0 g, 0.127 mol), anhydrous potassium acetate (25 g, 0.25 mol), acetic anydride (25 g, 0.25 mol), and 10 ml acetic acid were combined in a 250-ml round-bottomed flask with overhead stirring and heated to 130° C. for 4 hours. The mixture was concentrated under vacuum, the solids dissolved in 95 ml acetonitrile: 5 ml water, filtered through charcoal and poured into 600 ml ice with stirring. The mixture was allowed to stand overnight at room temperature, then 9.62 g (30%) product collected by filtration as a medium brown solid (adequate for the next step without purification). ¹H-NMR (400 MHz, DMSO-d₆) δ 11.10 (s, 1H), 7.59 (quartet, J=9.91 Hz, 1H), 7.29 (t, J=10.36 Hz, 1H), 7.21 (d, J=8.20 Hz, 1H), 7.11 (t, J=8.48 Hz, 1H), 5.83 (m, 2H), 5.02 (s, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.57 (quintet, J=7.66 Hz, 1F) −113.88 (quartet, J=8.93 Hz, 1F). LC/MS t_r=4.29 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 254 nm, at 50° C.) ES-MS m/z 238 (M+H).

Step 3: Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one 4-[(2,4-difluorobenzyl)oxy]-pyridin-2(1H)-one (from Step 2) (8.60 g, 36.3 mmol) was stirred in 150 ml dimethylformamide and treated with N-chlorosuccinimide (5.4 g, 39.9 mmol). After 15 hours, the precipitate was collected by filtration (5.11 g, 52%) yeilding a lustrous white solid. The mother liquor was diluted to 500 ml with diethyl ether, providing 2.47 g (25%) in a second crop. ¹H-NMR (400 MHz, DMSO-d₆) δ 11.87 (s, 1H), 7.60 (quartet, J=6.34 Hz, 1H), 7.43 (d, J=7.58 Hz, 1H), 7.31 (dt, J=10.08, 2.21 Hz, 1H), 7.14 (dt, J=8.65, 1.79 Hz, 1H), 6.44 (d, J=7.49 Hz, 1H), 5.28 (s, 1H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.58 (quintet, J=7.75 Hz, 1F), −113.68 (quartet, J=8.68 Hz, 1F). LC/MS t_r=4.47 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 254 nm, at 50° C.) ES-MS m/z 272, 274 3:1 (M+H).

Step 4. Preparation of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzonitrile. 3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one (from step 3) (3.25 g, 11.9 mmol) was combined with Cs₂CO₃ (3.93 g, 12.1 mmol) in 50 ml dimethylformamide and heated to 70° C., stirring under nitrogen. 3,4,5-trifluorobenzonitrile (1.83 g, 11.9 mmol) was added. After 4 hours, the mixture was filtered, concentrated in vacuo, washed thrice with hot cyclohexane, dissolved in tetrahydrofuran, treated with MgSO₄ and charcoal, and filtered. The solution was evaporated leaving a fine white solid (3.99 g, 82%). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.12 (d, J=7.59 Hz, 2H), 7.92 (d, J=8.31 Hz, 1H), 7.65 (quartet, J=6.77, 1H), 7.34 (dt, J=9.81, 2.71 Hz, 1H), 7.16 (dt, J=8.59, 2.50 Hz, 1H), 6.87 (d, J=8.01 Hz, 1H), 5.39 (s, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.17 (quintet, J=8.97 Hz, 1F), −113.51 (quartet, J=9.53 Hz, 1F), −116.32 (d, J=7.69 Hz, 2F). LC/MS t_r=5.51 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 409 (M+H). ES-HRMS m/z 409.0351 (M+H calcd for C₁₉H₁₀ClF₄N₂O₂ requires 409.0361).

Example 344

Preparation of 1-[4-(aminomethyl)-2,6-difluorophenyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one Hydrochloride

Step 1. Preparation of tert-butyl 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzylcarbamate. 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzonitrile (2.84 g, 6.95 mmol), di-t-butyl-dicarbonate (3.18 g, 14.6 mmol), and nickel(II) chloride (0.90 g, 6.95 mmol) were combined with 40 ml methanol and 40 ml tetrahydrofuran and cooled to 0° C. stirring in an ice bath. Sodium borohydride (1.33 g, 35.2 mmol) was added in small portions over 10 minutes to control foaming, and the reaction was stirred 1 hour. Additional sodium borohydride (0.50 g, 13.2 mmol) was required to force the reaction to completion by LC. A color change from yellow to black persisted on completion. The mixture was filtered through a bed of charcoal layered on anhydrous MgSO₄ and evaporated to dryness. Excess di-t-butyl-dicarbonate and byproduct t-butanol were removed by repeated heating with water to 80° C. in vacuo, giving the product as a fine white powder (3.11 g, 87%). ¹H-NMR (400 MHz, DMSO-d₆) δ 7.89 (d, J=8.04 Hz, 1H), 7.65 (quartet, J=6.73 Hz, 1H), 7.55 (t, J=6.73 Hz, 1H), 7.34, (dt, J=10.05, 2.51 Hz, 1H), 7.16 (m, 3H), 6.77 (d, J=8.18 Hz, 1H), 5.34 (s, 2H), 4.18 (d, J=5.68 Hz, 2H), 1.34 (s, 9H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.26 (quintet, J=6.91 Hz, 1F), −113.53 (quartet, J=7.73 Hz, 1F), −120.32(d, J=8.91 Hz, 2F). LC/MS t_r=5.90 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 513 (M+H). ES-HRMS m/z 513.1164 (M+H calcd for C₂₄H₂₂ClF₄N₂O₄ requires 513.1199).

Step 2: Preparation of 1-[4-(aminomethyl)-2,6-difluorophenyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one hydrochloride. Tert-butyl 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzylcarbamate (from step 3) (1.39 g, 2.71 mmol) was dissolved in 20 ml tetrahydrofuran and treated with 4 ml concentrated hydrochloric acid. The solution was evaporated and dried in vacuo to a fine white solid (1.20 g, 99%). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.54 (m, 2H), 7.86 (d, J=7.57 Hz, 1H), 7.65 (quartet, J=7.62, 1H), 7.50 (d, J=9.25 Hz, 2H), 7.34 (dt, J=10.50, 2.45 Hz, 1H), 7.16 (dt, J=8.38, 2.55 Hz, 1H), 6.78 (d, J=7.86 Hz, 1H), 5.37 (s, 2H), 4.10 (br s, 2H), 4.97-3.14 (v br s, 3H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.21 (quintet, J=7.77 Hz, 1F), −113.51 (quartet, J=8.95 Hz, 1F), −119.56 (d, J=9.44 Hz, 2F). LC/MS t_r=4.33 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 413 (M+H). ES-HRMS m/z 413.0712 (M+H calcd for C₁₉H₁₄ClF₄N₂O₂ requires 413.0674).

Example 345

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(methylamino)methyl]phenyl}pyridin-2(1H)-one Hydrochloride

Step 1. Preparation of tert-butyl 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl(methyl)carbamate. Tert-butyl 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzylcarbamate (from Step 1) (252 mg, 0.491 mmol) and iodomethane (75 mg, 0.528 mmol) are combined in 8 ml anhydrous dimethylformamide. Sodium hydride 60% in mineral oil (30 mg, 0.75 mmol) was added and the mixture stirred under nitrogen at room temperaure for 1 hour. Saturated aqueous NH₄Cl was added (4 ml) followed by 20 ml water and the product was extracted into ethyl acetate, washed with brine, dried over MgSO₄, filtered, and evaporated to give the product as a white powder (208 mg, 80%). ¹H-NMR (400 MHz, DMSO-d₆) δ 7.87 (d, J=7.85 Hz, 1H), 7.64 (quartet, J=6.66 Hz, 1H), 7.32, (dt, J=9.39, 3.29 Hz, 1H), 7.13 (m, 3H), 6.77 (d, J=7.94 Hz, 1), 5.38 (s, 2H), 4.43 (s, 2H), 2.90 (s, 3H), 1.40 (br m, 9H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.25 (quintet, J=8.93 Hz, 1F), −113.53 (quartet, J=9.73 Hz, 1F), −119.89(d, J=9.35 Hz, 2F). LC/MS t_r=6.16 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes, then 95% acetonitrile for 2 minutes, at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 527 (M+H). ES-HRMS m/z 527.1338 (M+H calcd for C₂₅H₂₄ClF₄N₂O₄ requires 527.1355).

Step 2. Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(methylamino)methyl]phenyl}pyridin-2(1H)-one hydrochloride. Tert-butyl 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl(methyl)carbamate (from step 1) (188 mg, 0.357 mmol) was subjected to the conditions of Step 2, yielding a fine white solid (165 mg, 100%). ¹H-NMR (400 MHz, DMSO-d₆) δ 9.30 (br s, 2H), 7.89 (d, J=7.99 Hz, 1H), 7.65 (quartet, J=7.64, 1H), 7.55 (d, J=8.66 Hz, 2H), 7.34 (dt, J=9.93, 2.57 Hz, 1H), 7.17 (dt, J=8.49, 2.48 Hz, 1H), 6.81 (d, J=8.01 Hz, 1H), 5.39 (s, 2H), 4.21 (s, 2H), 2.56 (s, 3H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.20 (quintet, J=7.56 Hz, 1F), −113.52(quartet, J=9.67 Hz, 1F), −119.21 (d, J=8.79 Hz, 2F). LC/MS t_r=4.30 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 427 (M+H). ES-HRMS m/z 427.0816 (M+H calcd for C₂₀H₁₆ClF₄N₂O₂ requires 427.0831).

Example 346

Preparation of 3-chloro-1-(4-{[(cyclopropylmethyl)amino]methyl}-2,6-difluorophenyl)-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one Hydrochloride

The title compound was prepared by direct analogy with procedures described above for 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(methylamino)methyl]phenyl}pyridin-2(1H)-one hydrochloride, replacing iodomethane with bromocyclopropylmethane and extending the reaction time to 6 hours in Step 1.

Step 1. Preparation of tert-butyl 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl(cyclopropylmethyl)carbamate

¹H-NMR (400 MHz, DMSO-d₆) δ 7.89 (d, J=7.91 Hz, 1H), 7.65 (quartet, J=6.81 Hz, 1H), 7.33, (dt, J=9.90, 2.26 Hz, 1H), 7.17 (m, 3H), 6.77 (d, J=7.90 Hz, 1), 5.38 (s, 2H), 4.51 (s, 2H), 3.10 (br s, 2H), 1.36 (m, 9H), 0.97 (br s, 1H), 0.38 (m, 2H), 0.18 (m, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.25 (quintet, J=7.77 Hz, 1F), −113.54 (quartet, J=9.02 Hz, 1F), −120.24 (m, 2F). LC/MS t_r=5.99 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes, then 95% acetonitrile for 2 minutes, at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 567 (M+H). ES-HRMS m/z 567.1653 (M+H calcd for C₂₈H₂₈ClF₄N₂O₄ requires 567.1668).

Step 2. Preparation of 3-chloro-1-(4-{[(cyclopropylmethyl)amino]methyl}-2,6-difluorophenyl)-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one hydrochloride. ¹H-NMR (400 MHz, DMSO-d₆) δ 9.51 (br s, 2H), 7.87 (d, J=7.96 Hz, 1H), 7.63 (m, 3H), 7.33 (dt, J=9.93, 2.65 Hz, 1H), 7.16 (dt, J=8.36, 2.32 Hz, 1H), 6.81 (d, J=7.92 Hz, 1H), 5.38 (s, 2H), 4.22 (br s, 2H), 2.82 (br s, 2H), 1.10 (m, 1H), 0.57 (m, 2H), 0.36 (m, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.25 (quintet, J=7.69 Hz, 1F), −13.54(quartet, J=9.35 Hz, 1F), −120.24 (m, 2F). LC/MS t_r=4.55 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 467 (M+H). ES-HRMS m/z 467.1119 (M+H calcd for C₂₃H₂₀ClF₄N₂O₂ requires 467.1144).

Example 347

Preparation of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluoro-N,N-dimethylbenzamide

Step 1: Preparation of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzamide 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzonitrile (540 mg, 1.32 mmol) and potassium trimethylsilonate 90% (375 mg, 2.63 mmol) are combined in 8 ml anhydrous toluene and heated to reflux with stirring. After 10 minutes, the mixture allowed to cool then partitioned between saturated aqueous ammonium chloride and ethyl acetate. The aqueous layer is extracted twice with ethyl acetate, the combined organics are washed with brine, dried over MgSO₄, and evaporated in vacuo. The crude product is taken up in tetrahydrofuran and filtered through charcoal layered over silica gel, and the solution evaporated in vacuo to give the product as a white powder (468 mg, 83%). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.22 (br s, 2H), 7.92 (d, J=7.84 Hz, 1H), 7.78 (d, J=8.45, 2H), 7.65 (quartet, J=8.40 Hz, 1H), 7.34, (dt, J=10.09, 2.58 Hz, 1H), 7.17 (dt, J=8.72, 2.30 Hz, 1H), 6.83 (d, J=7.91 Hz, 1H), 5.39 (s, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.21 (quintet, J=7.43 Hz, 1F), −113.52 (quartet, J=9.62 Hz, 1F), −118.74 (d, J=8.88 Hz, 2F). LC/MS t_r=4.67 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes, then 95% acetonitrile for 2 minutes, at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 427 (M+H). ES-HRMS m/z 427.0454 (M+H calcd for C₁₉H₁₂ClF₄N₂O₃ requires 427.0467).

Step 2. Preparation of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluoro-N,N-dimethylbenzamide. 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzamide (from step 1) (243 mg, 0.357 mmol) was subjected to the conditions of Step 1, with the exception that two equivalents of sodium hydride 60% in mineral oil and iodomethane were used instead of one (46 mg, 0.69 mmol and 103 mg, 0.724 mmol respectively). ¹H-NMR (400 MHz, DMSO-d₆) δ 7.92 (d, J=7.76 Hz, 1H), 7.66 (quartet, J=7.33, 1H), 7.44 (d, J=7.59 Hz, 2H), 7.34 (dt, J=9.88, 2.63 Hz, 1H), 7.17 (dt, J=8.35, 2.06 Hz, 1H), 6.83 (d, J=7.55 Hz, 1H), 5.39 (s, 2H), 2.98 (s, 3H), 2.91 (s, 3H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.22 (quintet, J=8.10 Hz, 1F), −113.53(quartet, J=9.18 Hz, 1F), −118.88 (d, J=7.77 Hz, 2F). LC/MS t_r=5.13 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 455 (M+H). ES-HRMS m/z 455.0791 (M+H calcd for C₂₁H₁₆ClF₄N₂O₃ requires 455.0780).

Example 348

Preparation of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3-fluoro-5-methoxybenzonitrile

Step 1. Preparation of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3-fluoro-5-hydroxybenzonitrile. 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzonitrile (522 mg, 1.28 mmol) and potassium trimethylsilonate 90% (655 mg, 4.60 mmol) are combined in 8 ml anhydrous tetrahydrofuran and stirred under nitrogen at room temperature for 2 hours. The precipitated potassium salt was collected by filtration, washed with a minimum of tetrahydofuran, and dried in vacuo. A portion of this salt (275 mg, 0.618 mmol) was dissolved in 5 ml water, the pH was adjusted below 6 with concentrated hydrochloric acid, the product collected by filtration, washed with water, sucked dry under a blanket of dry nitrogen, and dried further in vacuo overnight (251 mg, 100%, 98% overall). ¹H-NMR (400 MHz, DMSO-d₆) δ 11.46 (br s, 1H), 7.74 (d, J=7.81 Hz, 1H), 7.67 (quartet, J=6.76 Hz, 1H), 7.52 (d, J=8.76, 1H), 7.364, (dt, J=10.18, 2.37 Hz, 1H), 7.24 (br s, 1H), 7.17 (br t, J=8.75, 1H), 6.74 (d, J=8.04 Hz, 1H), 5.39 (s, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.26 (quintet, J=8.50 Hz, 1F), −113.52 (quartet, J=9.29 Hz, 1F), −118.06 (d, J=9.38 Hz, 1F). LC/MS t_r=5.13 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes, then 95% acetonitrile for 2 minutes, at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 407 (M+H). ES-HRMS m/z 407.0381 (M+H calcd for C₁₉H₁₁ClF₃N₂O₃ requires 407.0405).

Step 2. Preparation of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3-fluoro-5-methoxybenzonitrile. The potassium salt of 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3-fluoro-5-hydroxybenzonitrile (from Step 1) (273 mg, 0.614 mmol) was stirred in 5 ml anhydrous dimethylformamide under nitrogen. Iodomethane (93 mg, 0.66 mmol) was added, and stirring continued for 2 hr. The mixture was diluted to 50 ml with ice-cold water, and the white precipitate collected by filtration. The precipitate was washed thrice with water, sucked dry under a blanket of nitrogen, and dried further in vacuo overnight (242 mg, 87%). ¹H-NMR (400 MHz, DMSO-d₆) δ 7.73 (m, 2H), 7.65 (m, 2H), 7.34 (dt, J=9.90, 2.39 Hz, 1H), 7.17 (dt, J=8.75, 2.47 Hz, 1H), 6.75 (d, J=7.97 Hz, 1H), 5.37 (s, 2H), 3.84 (s, 3H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.24 (quintet, J=7.85 Hz, 1F), −113.54 (quartet, J=9.83 Hz, 1F), −118.33 (d, J=7.77 Hz, 1F). LC/MS t_r=5.40 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 421 (M+H). ES-HRMS m/z 421.0522 (M+H calcd for C₂₀H₁₃ClF₃N₂O₃ requires 421.0561).

Example 349

Preparation of N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}urea

1-[4-(aminomethyl)-2,6-difluorophenyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one hydrochloride (162 mg, 0.361 mmol) is dissolved in 4 ml 50% aqueous acetic acid and treated with potassium cyanate (59 mg, 0.72 mmol). The mixture was stirred 2 hr, then the mixture was diluted to 50 ml with cold water, and the crude product, contaminated with the acetamide, was purified by silica gel chromatography, eluting first with 20% ethanol in hexane then 40% ethanol in hexane. The 50% fractions were pooled by TLC and evaporated, giving the product as a fine white powder (65 mg, 40%). ¹H-NMR (400 MHz, DMSO-d₆) δ 7.87 (d, J=8.07 Hz, 1H), 7.64 (quartet, J=6.53 Hz, 1H), 7.33, (dt, J=9.47, 1.99 Hz, 1H), 7.15 (m, 3H), 6.76 (d, J=7.97 Hz, 1H), 6.59 (m, 1H), 5.65 (br s, 2H), 5.38 (s, 2H), 4.22 (m, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.22 (quintet, J=7.86 Hz, 1F), −113.51 (quartet, J=9.40 1F), −120.65 (d, J=8.75 Hz, 2). LC/MS t_r=4.85 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 456 (M+H).

Example 350

Preparation of 2-({4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}amino)-1,1-dimethyl-2-oxoethyl Acetate

1-[4-(aminomethyl)-2,6-difluorophenyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one hydrochloride (225 mg, 0.501 mmol) is dissolved in a solution of 10 ml tetrahydrofuran and triethylamine (111 mg, 1.10 mmol). 2-acetoxy-2-methyl-propionyl chloride (85 mg, 0.516 mmol) is added, and the mixture stirred for 30 minutes before partitioning between saturated aqueous ammoniom chloride and ethyl acetate. The layers are seperated, and the aqueous phase extracted twice with ethyl acetate. The combined organics are washed with water and brine, then dried over MgSO₄, filtered, and evaporated in vacuo, giving the product as a fine white powder (254 mg, 94%). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.47 (t, J=6.16 Hz, 1H), 7.88 (d, J=7.71 Hz, 1H), 7.65 (quartet, J=7.24 Hz, 1H), 7.34, (dt, J=10.04, 2.49 Hz, 1H), 7.16 (m, 3H), 6.77 (d, J=7.78 Hz, 1H), 5.38 (s, 2H), 4.32 (d, J=5.93 2H), 2.02 (s, 3H), 1.48(s, 6H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.26 (quintet, J=9.00 Hz, 1F), −113.52 (quartet, J=9.52 Hz, 1F), −120.62 (d, J=9.09 Hz, 2F). LC/MS t_r=5.43 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 541 (M+H). ES-HRMS m/z 541.1128 (M+H calcd for C₂₅H₂₂ClF₄N₂O₅ requires 541.1148).

Example 351

Preparation of N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}acetamide

The compound was prepared in the following the produre for Example 350, substituting acetyl chloride (24 mg, 0.30 mmol) for 2-acetoxy-2-methyl-propionyl chloride. (128 mg, 96%). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.48 (br s, 1H), 7.87 (d, J=7.28 Hz, 1H), 7.64 (quartet, J=8.01 Hz, 1H), 7.33, (dt, J=9.87, 2.25 Hz, 1H), 7.17 (m, 3H), 6.76 (d, J=8.25 Hz, 1H), 5.38 (s, 2H), 4.30 (m, 2H), 1.88(s, 3H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.22 (quintet, J=8.04 Hz, 1F), −113.52 (quartet, J=9.91 Hz, 1F), −120.43 (d, J=8.77 Hz, 2F). LC/MS t_r=5.04 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 555 (M+H). ES-HRMS m/z 455.0824 (M+H calcd for C₂₁H₁₆ClF₄N₂O₃ requires 455.0780).

Example 352

Preparation of N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}-2-methoxyacetamide

The compound was prepared in the following the produre for EXAMPLE 350, substituting 2-methoxy-acetyl chloride (45 mg, 0.415 mmol) for 2-acetoxy-2-methyl-propionyl chloride. (124 mg, 78%). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.56 (t, J=6.77 Hz, 1H), 7.90 (d, J=7.85 Hz, 1H), 7.67 (quartet, J=7.67 Hz, 1H), 7.36, (dt, J=10.03, 2.36 Hz, 1H), 7.20 (m, 3H), 6.79 (d, J=8.07 Hz, 1H), 5.40 (s, 2H), 4.37 (d, J=6.28 Hz, 2H), 3.91(s, 2H), 3.35 (s, 3H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.23 (quintet, J=8.29 Hz, 1F), −113.50 (quartet, J=9.36 Hz, 1F), −120.43 (d, J=9.07 Hz, 2F). LC/MS t_r=5.13 miinutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 485 (M+H). ES-HRMS m/z 485.0856 (M+H calcd for C₂₂H₁₈ClF₄N₂O₄ requires 485.0886).

Example 353

Preparation of N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}-2-furamide

The compound was prepared in the following the produre for Example 350, substituting furoyl chloride (62 mg, 0.48 mmol) for 2-acetoxy-2-methyl-propionyl chloride. Yield: 142 mg, 85%. ¹H-NMR (400 MHz, DMSO-d₆) δ 9.07 (t, J=6.14 Hz, 1H), 7.90 (d, J=7.88 Hz, 1H), 7.87 (dd, J=1.69, 0.80 Hz, 1H), 7.67 (td, J=8.46, 6.80 Hz, 1H), 7.35, (dt, J=10.00, 2.81 Hz, 1H), 7.26 (d, J=8.78 Hz, 2H), 7.18 (ddt, J=8.58, 2.30, 1.07 Hz, 1H), 7.16 (dd, J=3.52, 0.77 Hz, 1H), 6.79 (d, J=8.07 Hz, 1H), 6.64 (dd, J=3.16, 1.73 Hz, 1H), 5.40 (s, 2H), 4.49 (d, J=6.13 Hz, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.23 (quintet, J=7.65 Hz, 1F), −113.50 (quartet, J=9.84 Hz, 1F), −120.29 (d, J=9.41 Hz, 2F). LC/MS t_r=5.32 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 507 (M+H). ES-HRMS m/z 507.0716 (M+H calcd for C₂₄H₁₆ClF₄N₂O₄ requires 507.0729).

Example 354

Preparation of N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}-1H-imidazole-4-carboxamide

Step 1: Preparation of the title compound

1-[4-(aminomethyl)-2,6-difluorophenyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one hydrochloride (150 mg, 0.334 mmol) is dissolved in a solution of 4 ml tetrahydrofuran and triethylamine (35 mg, 0.35 mmol). 4-imidazolecarboxylic acid (62 mg, 0.56 mmol), 1-hydroxybenzotriazole hydrate (90 mg, 0.67 mmol), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (128 mg, 0.668 mmol), and triethylamine (100. mg, 0.989 mmol) were combined in 5 ml tetrahydrofuran and stirred under nitrogen. The solution containing 1-[4-(aminomethyl)-2,6-difluorophenyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one hydrochloride was added in one portion, rinsing with 2 ml tetrahydrofuran. Stirring was continued at room temperature overnight, then the reaction was poured into 90 ml of icewater, and the product collected by filtration and dired in vacuo (254 mg, 94%). ¹H-NMR (400 MHz, DMSO-d₆) δ 12.55 (br s, 1H), 8.73 (t, J=6.57 Hz, 1H), 7.90 (d, J=7.87 Hz, 1H), 7.75 (s, 1H), 7.67 (m, 2H), 7.35, (dt, J=10.04, 2.54 Hz, 1H), 7.21 (m, 3H), 6.78 (d, J=8.04 Hz, 1H), 5.39 (s, 2H), 4.47 (m, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.26 (quintet, J=7.87 Hz, 1F), −113.52 (quartet, J=9.30 Hz, 1F), −120.59 (d, J=9.21 Hz, 2F). LC/MS t_r=4.48 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 507 (M+H). ES-HRMS m/z 507.0818 (M+H calcd for C₂₃H₁₆ClF₄N₄O₃ requires 507.0842).

Example 355

Preparation of N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}-5-oxoprolinamide

The compound was prepared following the procedure for Example 354, substituting 2-pyrrolidone-5-carboxylic acid for 4-imidazolecarboxylic acid. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.67 (t, J=6.08 Hz, 1H), 7.88 (m, 1H), 7.65 (qr, J=7.57, 1H), 7.34, (dt, J=9.32, 2.63 Hz, 1H), 7.22 (d, J=9.36, 2H), 7.17 (dt, J=8.51, 2.55 Hz, 1H), 6.77 (d, J=7.66 Hz, 1H), 5.73 (s, 1H), 5.38 (s, 2H), 4.35 (d, J=5.74, 2H), 4.05 (m, 1H), 2.15 (m, 2H), 1.90 (m, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.25 (quintet, J=7.72 Hz, 1F), −113.52 (quartet, J=8.94 Hz, 1F), −120.39 (d, J=9.11 Hz, 2F). LC/MS t_r=4.81 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 524 (M+H). ES-HRMS m/z 524.0998 (M+H calcd for C₂₄H₁₉ClF₄N₃O₄ requires 524.0995).

Example 356

Preparation of

N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}-3-hydroxy-3-methylbutanamide

Step 1: Preparation of the title compound

The compound was prepared following the procedure for, substituting 2-hydroxy-2-methyl butyric acid for 4-imidazolecarboxylic acid. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.43 (t, J=6.04 Hz, 1H), 7.88 (d, J=8.01, 1H), 7.65 (qr, J=6.84, 1H), 7.34, (dt, J=10.13, 2.55 Hz, 1H), 7.22 (d, J=8.74, 2H), 7.16 (dt, J=8.57, 2.45 Hz, 1H), 6.77 (d, J=7.89 Hz, 1H), 5.38 (s, 2H), 4.75 (s, 0.5H (OH)), 4.35 (d, J=6.48, 2H), 2.28 (s, 2H), 1.47 (s, 0.5H(OH)), 1.16 (s, 6H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.26 (quintet, J=7.79 Hz, 1F), −113.53 (quartet, J=9.23 Hz, 1F), −120.49 (d, J=9.39 Hz, 2F). LC/MS t_r=5.08 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 513 (M+H). ES-HRMS m/z 513.1177 (M+H calcd for C₂₄H₂₂ClF₄N₂O₄ requires 513.1199).

Example 357

Preparation of N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,S-difluorobenzyl}-1-hydroxycyclopropanecarboxamide

The compound was prepared following the procedure for, substituting 1-hydroxy-1-cyclopropanecarboxylic acid for 4-imidazolecarboxylic acid. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.70 (t, J=6.26 Hz, 1H), 7.89 (d, J=6.31, 1H), 7.65 (qr, J=6.83, 1H), 7.34 (t, J=10.58 Hz, 1H), 7.19 (m, 3H), 6.77 (d, J=7.70 Hz, 1H), 5.38 (s, 2H), 4.35 (d, J=5.66, 2H), 1.14 (s, 1H), 1.02 (m, 2H), 0.84 (m, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.25 (quintet, J=8.05 Hz, 1F), −113.53 (quartet, J=8.27 Hz, 1F), −120.59 (d, J=8.99 Hz, 2F). LC/MS t_r=5.01 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 497 (M+H). ES-HRMS m/z 497.0873 (M+H calcd for C₂₃H₁₈ClF₄N₂O₄ requires 497.0886).

Example 358

Preparation of N-{4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl}-2-hydroxy-2-methylpropanamide

The compound was prepared following the procedure for, substituting 2-hydroxyisobutyric acid for 4-imidazolecarboxylic acid. ¹H-NMR (400 MHz, DMSO-d₆) δ 8.48 (t, J=6.41 Hz, 1H), 7.89 (d, J=7.78, 1H), 7.65 (qr, J=9.10, 1H), 7.33 (dt, J=10.12, 2.41 Hz, 1H), 7.17 (m, 3H), 6.77 (d, J=7.69 Hz, 1H), 5.38 (s, 2H), 4.31 (d, J=6.50, 2H), 1.41 (s, 1H), 1.33 (s, 6H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.25 (quintet, J=7.49 Hz, 1F), −113.53 (quartet, J=9.64 Hz, 1F), −120.59 (d, J=8.68 Hz, 2F). LC/MS t_r=5.05 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 499 (M+H). ES-HRMS m/z 499.1020 (M+H calcd for C₂₃H₂₀ClF₄N₂O₄ requires 499.1042).

Example 359

Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzonitrile

Step 1: Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one. The compound was prepared in the following the produre for 3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one (Step 3), substituting N-bromosuccinimide for N-chlorosuccinimide. ¹H-NMR (400 MHz, DMSO-d₆) δ 11.85 (br s, 1H), 7.61 (m, 1H), 7.46 (d, J=7.36 Hz, 1H), 7.30, (m, 1H), 7.14 (m, 1H), 6.40 (d, J=7.71 Hz, 1H), 5.26 (s, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.69 (quintet, J=7.93 Hz, 1F), −113.63 (quartet, J=9.55 Hz, 1F). LC/MS t_r=4.48 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 316 (M+H).

Step 2: Preparation of the title compound. The compound was prepared following the procedure for 4-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzonitrile (Step 4), substituting 3-bromo-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one (from step 1) (1.92 g, 6.06 mmol) for 3-chloro-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one (from Step 3). ¹H-NMR (400 MHz, DMSO-d₆) δ 8.13 (d, J=7.24 Hz, 2H), 7.95 (d, J=7.76 Hz, 1H), 7.66 (quartet, J=8.71 Hz, 1H), 7.34, (dt, J=9.94, 2.53 Hz, 1H), 7.17 (dt, J=8.64, 2.33 Hz, 1H), 6.82 (d, J=7.77 Hz, 1H), 5.39 (s, 2H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.28 (quintet, J=7.98 Hz, 1F), −113.45 (quartet, J=9.29 Hz, 1F), −116.30 (d, J=7.44 Hz, 2F). LC/MS t_r=5.48 minutes (0-95% acetonitrile/water, 0.05% trifluoroacetic acid, over 6 minutes at 1 ml/min with detection at 215 nm, at 50° C.) ES-MS m/z 453 (M+H). ES-HRMS m/z 452.9836 (M+H calcd for C₁₉H₁₀BrF₄N₂O₂ requires 452.9856).

Example 360

Preparation of 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(2-phenylethyl)pyridin-2(1H)-one

Step 1: Preparation of 1-(3-fluorobenzyl)-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 4-hydroxy-6-methyl-2-pyrone (2.5 g, 0.02 mol) and 3-fluorobenzylamine (2.5 g, 0.02 mol) in n-butanol (15.0 mL) was heated to reflux for 16 h under argon atmosphere. Butanol wad distilled in vacuo, the residue was triturated with EtOAc, cooled and filterd the precipitate. It was washed with cold EtOAc, and dried to give 0.86 g of the title compound as a pale yellow powder: 1H-NMR (CD3OD/400 MHz) δ 7.31 (m, 1H), 7.0-6.85 (m, 2H), 6.83 (d, 1H, J=9.6 Hz), 5.96 (d, 1H, j=2.0 Hz), 5.80 (d, 1H, J=2.0 Hz), 5.30 (s, 2H), and 2.24 (s, 3H); ESMS m/z=234 (MH+).

Step 2: Preparation of 3-bromo-1-(3-fluorobenzyl)-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 1-(3-fluorobenzyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.8 g, 0.0034 mol), NBS (0.64 g, 0.0036 mol) in dichloromethane (15.0 mL) was stirred at room temperature, under argon atmosphere. After 1.5 h, the reaction mixture was diluted with dichloromethane (15.0 mL), cooled and filterd the solids. The residue was washed with dichloromethane and dried in vacuo to give 0.93 g of the title compound as a white powder: 1H-NMR (CD3OD/400 MHz) δ 7.33 (m, 1H), 7.2-6.8 (m, 3H), 6.07 (s, 1H), 5.34 (s, 2H), 2.26 (s, 3H); ESHRMS m/z 312.0016 (M+H C13H12NO2BrF requires 312.0035).

Step 3: Preparation of 3-bromo-1-(3-fluorobenzyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate To a suspension of 3-bromo-1-(3-fluorobenzyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.86 g, 0.0028 mol) in dichloromethane (15.0 mL) cooled to −30° C., triethyl amine (0.5 mL, 0.004 mol) and trflic anhydride (0.7 mL, 0.0042 mol) were added and stirred for 1 h. The resulting orange solution was poured into ice cold water (25 mL) and extracted with dichloromethane (2×25 mL) The combined organic extracts were washed with water, dried (Na2SO4) and concentrated under reduced pressure. The resulting residue was purified by silica gel flash chromatography using 1:1 EtOAc/hexane v/v to afford 1.0 g (85%) the title compound as a light brown solid: ¹H-NMR (CDCl3/400 MHz) δ 7.32 (m, 1H), 7.0-6.85 (m, 3H), 6.18 (s, 1H), 5.32 (s, 2H), and 2.34 (s, 3H); ESHRMS m/z 443.9492 (M+H C14H11NO4BrF4S requires 443.9528).

Step 4: Preparation of 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(phenylethynyl)pyridin-2(1H)-one A solution of 3-bromo-1-(3-fluorobenzyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate (1.0 g, 0.0022 mol) and phenylacetylene (0.3 mL, 0.0029 mol) in DMF (5.0 mL) was degassed using house vacuum, and purged with argon (3 cycles). Then added diisopropylethylamine, (0.5 mL) followed by the addition of PdCl2(PPh3)2 (0.36 g). The reaction mixture was heated at 65° C. for 1.5 h under argon atmosphere. The solvents were distilled in vacuo, and the residue was purified by silica gel flash chromatography using EtOAc/hexane (2:3 v/v) to afford 0.65 g (70%) of the title compound as a brown colored amorphous solid: ¹H-NMR (CD3OD/400 MHz) δ 7.59 (m, 2H), 7.45-7.3 (m, 4H), 7.05-6.85 (m, 3H), 6.44 (s, 1H), 5.41 (s, 2H), and 2.31 (s, 3H); ¹⁹F-NMR (CD3OD/400 MHz) δ −116.33 (m); ESHRMS m/z 396.0373 (M+H C21H16NOBrF 396.0399).

Step 5: Preparation of 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(2-phenylethyl)pyridin-2(1H)-one. To a solution of 3-bromo-1-(3-fluorobenzyl)-6-methyl-4-(phenylethynyl)pyridin-2(1H)-one (0.55 g, 0.0014 mol) in EtOAc (10.0 mL) and EtOH (10.0 mL) was added PtO2 (0.05 g) and stirred in an atmosphere of hydrogen gas at 15 psi for 30 min. The catalyst was removed by filtration, the filtrate was concentrated and the residue was purified by silica gel flash chromatography using 25% EtOAc in hexane as the eluent. The appropriate fractions were combined (visualized under UV) and concentrated to dryness. ¹H-NMR (CD3OD/400 MHz) δ 7.35 (m, 1H), 7.31-7.16 (m, 5H), 6.99(m, 1H), 6.91 (m, 1H), 6.81 (m, 1H), 6.20 (s, 1H), 5.41 (s, 2H), 2.94 (m, 4H), and 2.24 (s, 3H); ¹⁹F-NMR (CD3OD/400 MHz) δ −115.01 (m); ESHRMS m/z 400.0695 (M+H C21H20NOBrF 400.0712).

Example 361

Preparation of 3-bromo-1-(3-fluorobenzyl)-4-(1-phenylethoxy)pyridin-2(1H)-one

A mixture of 3-bromo-1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one (0.2 g, 0.72 mmol), potassium carbonate (0.1 g, 0.72 mmol) and (1-bromoethyl)benzene (0.19 g, 1 mmol) in DMF (3.0 mL) was stirred at room temperature for 16 h. DMF was distilled in vacuo, and the residue was purified by flash chromatography (EtOAc in hexane (1:3 v/v) to give pale yellow syrup. This material was further purified by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min), at flow rate of 100 ml/min. The appropriate fractions were combined, concentrated to a small volume (20 mL), added EtOAc (25 mL) and washed successively with satd. sod. bicarbonate, water, and dried (Na₂SO₄). EtOAc was removed under reduced pressure and residue was dried in vacuo to afford the title compound (0.15 g, 52%) as an amorphous substance: ¹H NMR (CD₃OD/400 MHz) δ 7.56 (d, 1H, J=7.6 Hz), 7.4-7.2 (m, 5H), 7.0 (m, 3H), 6.28 (d, 1H, J=7.6 Hz), 5.65 (m, 1H), 5.19 (d×d, 2H, J=14.8 Hz), and 1.64 (d, 3H, J=6.4 Hz), ES-HRMS m/z 402.0492(M+H C₂₀H₁₈NO₂Br, requires 402.0499).

Example 362

Preparation of 3-bromo-1-(3-fluorobenzyl)-4-[(E)-2-(4-fluorophenyl)ethenyl]pyridin-2(1H)-one

A mixture of 3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl trifluoromethanesulfonate (1.0 g, 0.0023 mol), and 4-fluorostyrene (0.33 mL, 0.0028 mol) in degassed DMF (10 0 ml) containing diisopropyl ethyl amine (0.37 g, 0.0029 mol) was treated with PdCl₂(PPh₃)₂ (0.32 g, 0.46 mmol) and heated at 65° C. under argon atmosphere for 16 h. DMF was distilled in vacuo, and the residue was purified by flash chromatography (EtOAc/hexane 1:4 v/v) to afford a yellow substance which was further purified by by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min), at flow rate of 100 ml/min. The appropriate fractions were combined, concentrated to a small volume (20 mL), added EtOAc (25 mL) and washed successively with satd. sod. bicarbonate, water, and dried (Na₂SO₄). EtOAc was removed under reduced pressure and residue was dried in vacuo to afford the title compound (0.06 g, 6%) as yellow powder: ¹H NMR (CD₃OD/400 MHz) δ 7.68 (m, 3H), 7.39 (m, 3H), 7.2-7.0 (m, 5H), 6.82 (d, 1H, J=7.2 Hz), and 5.22 (s, 2H); ¹⁹F NMR(CD₃OD/400 MHz) δ −113.9 (m) and −115 (m); ES-HRMS m/z 402.0305 (M+H C₂₀H₁₅NOF₂Br, requires 402.0300).

Example 363

Preparation of 4-(benzyloxy)-3-bromo-1-[(6-fluoropyridin-3-yl)methyl]pyridin-2(1H)-one

A mixture of 4-(benzyloxy)-3-bromopyridin-2(1H)-one (0.2 g, 0.00076 mol), 5-bromomethyl-2-fluoropyridine (0.25 g, 0.0013 mol) and pot. Carbonate (0.15 g, 0.0011 mol) in DMF (3.0 ml) was stirred at room temperature for 16 h under argon atmosphere. DMF was distilled in vacuo and the residue was partitioned between water (15 ml) and EtOAc (25 mL). The organic phase was washed with water, dried (Na₂SO₄) and concentrated under reduced pressure. ¹H NMR (CD₃OD/400 MHz) δ 8.22 (m, 1H, 2.4 Hz), 7.92 (m, 1H), 7.82 (d, 1H, J=7.6 Hz), 7.44-7.31 (m 5H), 7.03 (m, 1H) 6.49 (d, 1H, J=7.6 Hz), 5.29 (s, 2H), and 5.20 (s, 2H); ¹⁹F NMR(CD₃OD/400 MHz) δ −72.30 (d, J=6.0 Hz) and −115 (m); ES-HRMS m/z 389.0295 (M+H C₁₈H₁₅N₂O₂FBr, requires 389.0309).

Example 364

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-dimethylphenyl)-6-methylpyridin-2(1H)-one

Step 1. Preparation of 1-(2,6-dimethylphenyl)-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 4-hydroxy-6-methyl-2-pyrone (2.5 g, 0.02 mol), 2,6 dimethylaniline (2.4 g, 0.02 mol), and p-toluenesulfonic acid (0.2 g) as heated at 140° C. for 3 h under nitrogen atmosphere. The reaction mixture was cooled, triturated with acetonitrile, cooled and filtered the solids. ¹H NMR (CD₃OD/400 MHz) δ 7.22 (m, 3H), 6.12 (d, 1H, J=1.6 Hz), 5.83 (d, 1H, J=1.8 Hz), 2.00 (s, 6H), and 1.82 (s, 3H); ESMS m/z 229 (M+H).

Step 2. Preparation of 3-bromo-1-(2,6-dimethylphenyl)-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 1-(2,6-dimethylphenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.4 g, 0.00175 mol), and NBS (0.35 g, 0.0019 mol) in dichloromethane (10.0 ml) was stirred at room temperature under nitrogen atmosphere. After 1 h, the solids were filtered, washed with dicholoromethane to give 0.42 g (78%) of the title compd as a pale yellow powder: 1H NMR (CD₃OD/400 MHz) δ 7.22 (m, 3H), 6.21 (s, 1H), 1.99 (s, 6H), and 1.82 (s, 3H); ESMS m/z 308/310 (M+H).

Step 3. A mixture of 3-Bromo-1-(2,6-dimethylphenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.15 g, 0.00049 mol), 2,4 difluorobenzyl bromide (0.12 g, 0.00058 mol) and potassium carbonate (0.075 g, 0.00054 mol) in DMF 3.00 mL) was stirred at room temperature uder argon atmosphere for 2 h. It was then heated at 60° C. for 30 min and concentrated in vacuo. The residue was purified by flash chromatography. ¹H NMR (CD₃OD/400 MHz) δ 7.62 (m, 1H), 7.28 (m, 3H), 7.04 (m, 2H), 6.68 (s, 1H), 5.35 (m, 1H), 1.98 (s, 6H), and 1.92 (s, 3H); ES-HRMS m/z 434.0574 (M+H C₂₁H₁₉NO₂F₂Br, requires 434.0562).

Example 365

Preparation of 3-bromo-1-(2,6-dimethylphenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described for Example 364. ¹H NMR (CD₃OD/400 MHz) δ 7.58 (m, 2H), 7.23 (m, 3H), 7.15 (m, 2H), 6.62 (s, 1H), 5.32 (s, 2H), 1.98 (m, 6H), and 1.91 (s, 3H); ES-HRMS m/z 416.0670. (M+H C₂₁H₂₀NO₂FBr, requires 416.0656).

Example 366

Preparation of 3-bromo-1-(2,6-dimethylphenyl)-6-methyl-4-[(2,4,6-trifluorobenzyl)oxy]pyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described for EXAMPLE 364. ¹H NMR (CD₃OD/400 MHz) δ 7.19 (m, 3H), 6.95 (m, 2H), 6.69 (s, 1H), 5.29 (s, 2H), 1.95 (s, 6H), and 1.90 (s, 3H); ES-HRMS m/z 452.0471. (M+H C₂₁H₁₈NO₂F₃Br, requires 452.0468).

Example 367

Preparation of 3-bromo-4-[(2,6-difluorobenzyl)oxy]-1-(2,6-dimethylphenyl)-6-methylpyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described for EXAMPLE 364. ¹H NMR (CD₃OD/400 MHz) δ 7.46 (m, 1H), 7.24 (m, 3H), 7.08 (m, 2H), 6.74 (s, 1H), 5.38 (s, 2H), 1.99 (s, 6H), and 1.94 (s, 3H); ES-HRMS m/z 434.0589 (M+H C₂₁H₁₉NO₂F₂Br, requires 434.0562).

Example 368

Preparation of 3-bromo-1-(2,6-dichlorophenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1. Preparation of 1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one This compound was prepared by a procedure similar to the one described in step 1 for Example 364. Yield: 28%, ¹H NMR (CD3OD) δ 7.6 (m, 2H), 7.48 (m, 1H), 6.10 (dd, 1H), 5.78 (d, 1H, J=2.4 Hz), 1.91 (s, 3H); ES-MS m/z=270 (MH⁺).

Step 2. Preparation of 3-bromo-1-(2,6-dichlorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one This compound was prepared by a procedure similar to the one described in step 2 for Example 364. Yield: 78%, ¹H NMR (400 MHz) CD₃OD δ 7.61 (m, 2H), 7.49 (m, 1H), 6.2 (s, 1H), and 1.91 (s, 3H); ES-MS, m/z=348 (MH⁺).

Step 3. Preparation of 3-bromo-1-(2,6-dichlorophenyl)-4-[(4-fluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. This compound was prepared by a procedure similar to the one described in step 3 for EXAMPLE 364. Yield: 44%, ¹H NMR (CD₃OD) δ 7.62 (d, 2H, J=8.0 Hz), 7.51 (m, 3H), 7.15 (m, 2H), 6.64 (s, 1H), 5.33 (s, 2H), and 2.0 (s, 3H); ¹⁹F NMR (CD₃OD) δ −166.21 (m) □ES-HRMS m/z 455.9541(M+H C₁₉H₁₄NO₂Cl₂BrF, requires 455.9564).

Example 369

Preparation of 3-bromo-1-(2,6-dichlorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

This compound was prepared by a procedure similar to the one described for EXAMPLE 368. Yield: 64%, 1H NMR (CD₃OD/400 MHz δ 7.62 (m, 3H), 7.48 (m, 1H), 7.05 (m, 2H), 6.70 (s, 1H), 5.36 (s, 2H), and 2.02 (s, 3H) ¹⁹F NMR (CD₃OD) 6-111.43 (m) and −115.89 (m); ES-HRMS m/z 473.9450 (M+H C₁₉H₁₃NO₂Cl₂BrF₂, requires 473.9469).

Example 370

Preparation of 3-Bromo-1-(2,6-dichlorophenyl)-4-[(2,6-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

This compound was prepared by a procedure similar to the one described for Example 368. Yield: 78%, ¹H NMR (CD₃OD/400 MHz) δ 7.62 (d, 2H, J=8.0 Hz), 7.52 (m, 2H), 7.1 (m, 2H), 6.77 (s, 1H), and 2.04 (s, 3H); ¹⁹F NMR (CD₃OD) δ −117.04 (m); ES-HRMS m/z 473.9468 (M+H C₁₉H₁₃NO₂Cl₂BrF₂, requires 473.9469).

Example 371

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-methoxy-6-methylphenyl)-6-methylpyridin-2(1H)-one

Step 1. Preparation of 4-hydroxy-1-(2-methoxy-6-methylphenyl)-6-methylpyridin-2(1H)-one This compound was prepared by a procedure similar to the one described in step 1 for Example 368. Yield: 21%, ¹H NMR (CD₃OD/400 MHz) δ 7.31 (m, 1H), 6.94 (m, 2H), 6.05 (d, 1H, J=2.4 Hz), 5.78 (d, 1H, J=2.4 Hz), 3.76 (s, 3H), 2.00 (s, 3H), and 1.83 (s, 3H); ES-HRMS m/z 246.1092 (M+H C₁₄H₁₆NO₃, requires 246.1123).

Step 2. Preparation of 3-bromo-4-hydroxy-1-(2-methoxy-6-methylphenyl)-6-methylpyridin-2(1H)-one This compound was prepared by a procedure similar to the one described in step 2 for EXAMPLE 368. Yield: 58%, ¹H NMR (CD₃OD/400 MHz) δ 7.34 (m, 1H), 6.96 (m, 2H), 6.15 (s, 1H), 3.76 (s, 3H), 1.99 (s, 3H), and 1.83 (s, 3H); ESMS m/z 324 (M+H).

Step 3. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-methoxy-6-methylphenyl)-6-methylpyridin-2(1H)-one. This compound was prepared by a procedure similar to the one described for Example 368. Yield: 60%, ¹H NMR (CD₃OD/400 MHz) δ 7.63 (m, 1H), 7.36 (m, 1H), 7.01 (m, 4H), 6.61 (s, 1H), 5.33 (s, 2H), 3.76 (s, 3H), 1.99 (s, 3H), and 1.95 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.64 (m), and −116.03 (m); ES-HRMS m/z 450.0532 (M+H C₂₁H₁₉NO₃Cl₂BrF₂, requires 450.0511).

Example 372

Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-dichlorobenzenesulfonamide

Step 1. Preparation of 3,5-dichloro-4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzenesulfonamide A mixture of 4-hydroxy-6-methylpyrone ((1.2 g, 0.0095 mol), and 2,6-dichlorosulphanilamide (2.4 g, 0.0099 mol) was heated at 170° C. under argon for 20 min. The resulting dark colored melt was cooled and the crude material was first purified by flash chromatography (EtOAc) to give partially purified material which contained the desired product. This was further purified by reverse-phase HPLC using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=349) were combined and freeze dried to afford 0.19 g of 3,5-dichloro-4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzenesulfonamide as pale yellow solid: ¹H NMR (CD₃OD/400 MHz) δ 8.06 (s, 2H), 6/13 (d, 1H, J=1;6 Hz), 5.78 (d, 1H, J=1.6 Hz), and 1.94 (s, 3H)); ES-HRMS m/z 348.9819 (M+H C₁₂H₁₁N₂O₄SCl₂ requires 348.9811).

Step 2. Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-dichlorobenzenesulfonamide. A mixture of 3,5-dichloro-4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzenesulfonamide (0.18 g, 0.0005 mol), N-bromosuccinimide (0.1 g, 0.00056 mol) in acetici acid (2.0 mL) was stirred at room temperature under argon atmosphere for 1 h. Acetic acid was removed in vacuo, the residue was dissolved in DMF (2.0 mL), and added 2,4 difluorobenzyl bromide (0.128 g, 0.0006 mol), potassium carbonate (0.1 g, 0.0007 mol). The resulting mixture was stirred at room temperature for 1 h. The solvents were distilled in vacuo, and the residue was purified by flash chromatography (EtOAc/hexane 1:3 v/v) to give 0.14 g of partially purified product. This was further purified by reverse-phase HPLC using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=553) were combined and freeze dried to afford 0.045 g of pale yellow powder. This was partitioned between EtOAc (25 ml) and 5% sod. bicarbonate. The organic phase was washed with water, dried (Na₂SO₄) and concentrated under reduced pressure. This material was dried in vacuo to afford the title compound (0.033 g) as a white amorphous substance: ¹H NMR (CDCl₃/400 MHz) δ 7.99 (s, 2H), 7.59 (m, 1H), 6.98 (m, 1H), 6.85 (m, 1H), 6.23 (s, 1H), 5.69 (s, 2H), 5.28 (s, 2H), 1.97 (s, 3H), and 1.76 (br, 2H); ES-HRMS m/z 552.7214 (M+H C₁₉H₁₄BrCl₂N₂O₄S requires 552.9197).

Example 373

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one

Step 1. Preparation of 1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 4-hydroxy-6-methyl-2-pyrone (10.0 g, 0.079 mol) and 2,6 difluoroaniline (9.5 g, 0.073 mol) was heated at 170° C. under argon atmosphere for 20 min. The water formed was removed using a Dean-stark apparatus. The melt was cooled, the dark solid was tritutrated with EtOAc., and filtered. This material was washed thoroughly with EtOAc to afford the desired product 1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one 6.5 g (35%) as a light brown solid: ¹H NMR (CD₃OD/400 MHz) δ 7.56 (m, 1H), 7.19 (m, 2H), 6.09 (m, 1H), 5.77 (d, 1H, J=2.4 Hz), and 1.99 (s, 3H); ES-HRMS m/z 238.0679 (M+H C₁₂H₁₀NO₂F₂ requires 238.0674).

Step 2. Preparation of 3-bromo-1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one The title compound was prepared by a procedure described in step 2 for Example 364. Yield: 79%, ¹H NMR (CD₃OD/400 MHz) δ 7.58 (m, 1H), 7.21 (m, 2H), 6.19 (d, 1H, J=0.8 Hz), 1.99 (s, 3H); ES-HRMS m/z 315.9811 (M+H C₁₂H₉NO₂F₂Br requires 315.9779).

Step 3. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one. This compound was prepared by a procedure described in step 3 for EXAMPLE 364. Yield: 63%, ¹H NMR (CD₃OD) δ 7.58 (m, 2H), 7.23 (m, 2H), 7.06 (m, 2H), 6.68 (s, 1H), 5.36 (s, 2H), and 2.10 (s, 3H); ¹⁹F NMR (CD₃OD) δ −111.50 (m), −115.96 (m), and −121.93 (m); ES-HRMS m/z 442.0061 (M+H C₁₉H₁₃NO₂F₄Br requires 442.0060).

Example 374

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one

A solution of 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one (0.3 g, 0.00068 mol) and N-iodosuccinimide (0.22 g, 0.00098 mol) in dichloroethane, containing dichloroacetic acid (0.1 mL) was heated to reflux for 6 h under argon atmosphere. After the removal of the solvents under reduced pressure, the residue was partitioned between, dichloromethane (20 mL) and 5% sod. sulphite (10 mL). The organic phase was washed with water, dried (Na₂SO₄), and concentrated under reduced pressure. The residue was purified by flash chromatography (25% EtOAc in hexane) to afford the title compound (0.125 g, 32%) as a pale yellow powder: ¹H NMR (CDCl₃/400 MHz) δ 7.68 (m, 1H), 7.46 (m, 1H), 7.11 (m, 2H), 6.95 (m, 1H), 6.85 (m, 1H), 5.23 (s, 2H), and 2.38 (s, 3H); ¹⁹F NMR (CDCl₃) δ −109.15 (m), −112.95 (m), −118.50 (m); ES-HRMS m/z 567.9014 (M+H C₁₉H₁₂NO₂F₄BrI requires 567.9027).

Example 375

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2-(dimethylamino)-4,6-difluorophenyl]-6-methylpyridin-2(1H)-one

Step 1. Preparation of 3,5-difluoro-N˜1˜,N˜1˜-dimethylbenzene-1,2-diamine

To a solution of 2,4,6-trifluoronitrobenzene (2.58 g, 0.0145 mol) in THF (20.0 ml) was added a solution of N,N-dimethylamine in THF (8.5 mL of 2M soln) and stirred for 45 min at 0° C. It was then stirred at room temperature for 30 min and concentrated to dryness. The resulting material was dissolved in EtOH (25 mL), added Pd/C (10%, 0.6 g) and hydrogenated at 50 psi for 4 h. The catalyst was removed by filtration, and the filtrate was concentrated to dryness under reducued pressure. Te residue was partitioned between sod. bicarbonate (10%, 25 mL) and EtOAc (30 mL). The organic phase was washed with water, dried (Na₂SO₄), and concentrated to dryness to afford the title compound (1.3 g, 50%) as a dark colored solid: ¹H NMR (CDCl₃/400 MHz) δ 6.52 (m, 2H), 3.64 (br, 2H), and 2.65 (s, 6H); ES-HRMS m/z 172.0772 (M+C₈H₁₀N₂F₂ requires 172.0810).

Step 2. 1-[2-(dimethylamino)-4,6-difluorophenyl]-4-hydroxy-6-methylpyridin-2(1H)-one An intimate mixture of 4-hydroxy-6-methyl-2-pyrone (1.3 g, 0.0103 mol), and 3,5-difluoro-N,N-dimethylbenzene-1,2-diamine (1.4 g, 0.008 mol) was heated at 160° C. under argon for 15 min. The dark colored reaction mixture was cooled, triturated with EtOAc (15 ml), and filtered. The solids were washed with warm EtOAc, followed by hexane and dried to give the title compound as a light blue solid (0.4 g, 14%). Analalytically pure sample was prepared by reverse-phase HPLC purification using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions were combined and freeze-dried to give the title compound: ¹H NMR (CD₃OD/400 MHz) δ 6.61 (m, 2H), 6.08 (d, 1H, J=2.0 Hz), 6.78 (d, 1H, J=2.0 Hz), 2.69 (s, 6H), and 1.94 (s, 3H); ES-HRMS m/z 281.1084 (M+H C₁₄H₁₅N₂O₂F₂ requires 281.1096).

Step 3. Preparation of 3-bromo-1-[2-(dimethylamino)-4,6-difluorophenyl]-4-hydroxy-6-methylpyridin-2(1H)-one The title compound was prepared by a procedure described in step 2 for Example 364. Yield: 71%, ¹H NMR (CD₃OD/400 MHz) δ 6.62 (m, 2H), 6.17 (s, 1H), 2.67 (s, 6H), and 1.94 (s, 3H); ES-HRMS m/z 359.0188 (M+H C₁₄H₁₄N₂O₂F₂Br requires 359.0201).

Step 4 The product of Step 3 above was used in the procedure described in step 3 for Example 364. Yield: 34%, ¹H NMR (CDCl₃/400 MHz) δ 7.62 (m, 1H), 6.98 (m, 1H), 6.85 (m, 1H), 6.46 (m, 2H), 6.11(s, 1H), 5.24 (s, 2H), 2.66 (s, 6H), and 1.98 (s, 3H); ¹⁹F NMR (CDCl₃/400 MHz) δ −108.06 (m), −109.60 (m), −115.02 (m), and −116.01 (m); ES-HRMS m/z 485.0451 (M+H C₂₁H₁₈N₂O₂F₄Br requires 485.0482).

Step 5. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2-(dimethylamino)-4,6-difluorophenyl]-6-methylpyridin-2(1H)-one. The title compound was prepared by stirring a suspension of the product of step 4 above (0.14 g) with 4N HCl in dioxane (0.7 mL) at room temperature for 30 min. The mixture was concentrated to dryness. ¹H NMR (CD₃OD/400 MHz) δ 7.62 (m, 1H), 7.02 (m, 2H), 6.65 (m, 3H), 5.34 (s, 2H), 2.66 (s, 6H), and 2.05 (s, 3H); ESMS m/z=485.

Example 376

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,4-difluoro-6-[(2-hydroxyethyl)(methyl)amino]phenyl}-6-methylpyridin-2(1H)-one

The title compound was prepared by a similar procedure described for Example 375, replacing N,N-dimethyl group by N-Methyl-aminoethanol. ¹H NMR (CDCl₃/400 MHz) δ 7.59 (m, 1H), 6.98 (m, 1H), 6.85 (m, 1H), 6.61 (m, 1H), 6.52 (m, 1H), 6.17 (m, 1H), 5.25 (s, 2H), 3.63 (m, 1H), 3.53 (m, 1H), 3.26 (m, 1H), 3.0 (m, 1H), 2.66 (s, 6H), and 2.09 (s, 3H); ES-HRMS m/z 515.0512 (M+H C₂₂H₂₀N₂O₃F₄Br requires 515.0588).

Example 377

Preparation of 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzonitrile

Step 1. Preparation of 2-(bromomethyl)-5-fluorobenzonitrile A mixture of 5-fluoro-2-methylbenzonitrile (2.0 g, 0.015 mol), NBS (3.2 g, 0.018 mol) and benzoylperoxide (0.25 g) in carbontetrachloride (25.0 ml) was heated to reflux for 6 h, under argon atmosphere. The reaction mixture was cooled and filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by flash chromatography (5% EtOAc in hexane) to afford 2-(Bromomethyl)-5-fluorobenzonitrile (1.9 g, 60%) as a colorless liquid: ¹H NMR (CDCl₃/400 MHz) m) 7.58 (m, 1H), 7.38 (m, 1H), and 7.25 (m, 1H).

Step 2. Preparation of 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzonitrile. A mixture of 3-bromo-1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (1.0 g, 0.0032 mol), potassium carbonate (0.65 g, 0.0047 mol) and 2-(bromomethyl)-5-fluorobenzonitrile (0.95 g, 0.0045 mol) in dimethylacetamide (15.0 ml) was stirred at room temperature under argon atmosphere. After 1 h, dimethylacetamide was distilled in vacuo and the residue was partitioned between dichloromethane (50 ml) and 55 citric acid (15 mL). The organic phase was washed with water, dried (Na₂SO₄), and concentrated to dryness. The resulting material was triturated with EtOAc, filtered, washed with EtOAc and dried to afford the title compound (0.86 g, 60%) as a white powder: ¹H NMR (DMSO-d₆/400 MHz) δ 7.95 (m, 1H), 7.81 (m, 1H), 7.68 (m, 2H), 7.37 (m, 2H), 6.79 (s, 1H), 5.45 (s, 2H), and 2.03 (s, 3H); ¹⁹F-NMR (DMSO-d₆) δ −111.31 (m), −120.34 (m); ESHRMS m/z 449.0094 (M+H C₂₀H₁₃N₂O₂F₃Br requires 449.0107).

Example 378

Preparation of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate

To a cold suspension of 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzonitrile (0.3 g, 0.00066 mol) in THF (3.0 mL), was added BH₃.THF (1.0 mL). After stirring at room temperature for 15 min, the reaction mixture was heated to reflux for 30 min under argon atmosphere. The resulting clear solution cooled, added MeOH (2.0 mL), concentrated under reduced pressure, and the residue was purified by reverse-phase HPLC purification using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=453 M+H) were combined and freeze-dried to give the title compound (0.16 g, 43%) as its trifluoroacetate salt: ¹H NMR (DMSO-d_6/400 MHz) δ 8.19 (br, 3H), 7.65 (m, 2H), 7.37 (m, 4H), 6.78 (s, 1H), 5.42 (s, 2H), 4.21 (br, 2H), and 2.04 (s, 3H); ¹⁹F NMR (DMSO-dr/400 MHz) δ −112.96 (m), and −120.41 (m); ES-HRMS m/z 453.0387 (M+H C₂₀H₁₇N₂O₃F₃Br requires 453.0420).

Example 379

Preparation of N-[2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzyl]urea

To a suspension of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate (0.13 g, 0.00023 mol) in THF (3.0 mL), was added triethyl amine (0.07 mL, 0.0005 mol) followed by the addition of trimethylsilylisocyanate (0.066 mL). The reaction mixture was stirred at room temperature for 1 h, and the desired product was isolated by reverse-phase HPLC purification using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=496 M+H) were combined and freeze-dried, and the residue was partitioned between 5% sod. bicarbonate (20 mL) and dichloromethane (20 mL). The organic phase was washed with water, dried (Na₂SO₄) and concentrated to dryness under reduced pressure, to afford the title compound as a white amorphous powder (0.065 g): ¹H NMR (DMSO-d_6/400 MHz) δ 7.62 (m, 1H), 7.52 (m, 1H), 7.35 (m, 2H), 7.09 (m, 2H), 6.77 (s, 1H), 6.51 (t, 1H), 5.61 (s, 2H), 5.38 (s. 2H), 4.28 (d, 2H, J=6.0 Hz), and 2.02 (s, 3H); ¹⁹F NMR (DMSO-d₆/400 MHz) δ −114.044 (m), and −120.31 (m); ES-HRMS m/z 496.0460 (M+H C₂₁H₁₈N₃O₃F₃Br requires 496.0478).

Example 380

Preparation of Methyl 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

To solution of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate (0.12 g, 0.00021 mol) in dimethylacetamide (2.0 mL) at 0° C., was added triethylamine (0.06 mL, 0.00043 mol) followed by the addition of methylchloroformate (0.05 mL). The reaction mixture was stirred at room temperature for 30 min under argon atmosphere. Dimethylacetamide was distilled in vacuo and the residue was partitioned between dichloromethane (10 mL) and 5% citric acid (10 mL). The organic phase was washed with water, dried (Na₂SO₄) and concentrated to dryness. The resulting residue was purified by flash chromatography (60% EtOAc in hexane) to afford the title compound (0.09 g, 75%) as a white amorphous powder: ¹H NMR (DMSO-d_6/400 MHz) δ 7.68 (m, 1H), 7.62 (m, 1H), 7.59 (m, 1H), 7.38 (m, 2H), 7.115 (m, 2H), 6.78 (s, 1H), 5.38 (s, 2H), 4.31 (d, 2H, J=6.0 Hz), 3.53 (s, 3H), and 2.03 (s, 3H); ¹⁹F NMR (DMSO-d_6/400 MHz) δ −113.77 (m), and −120.33 (m); ES-HRMS m/z 511.0508 (M+H C₂₂H₁₉N₂O₄F₃Br requires 511.0475).

Example 381

Preparation of N-[2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzyl]-2-hydroxyacetamide

To a suspension of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate (0.12 g, 0.00021 mol) in THF (2.0 mL) at 5° C., was added triethyl amine (0.036 g, 0.00035 mol) followed by the addition of acetoxyacetyl chloride (0.05 mL). The mixture was stirred at room temperature for 30 min, diluted with cold water (10 mL), and extracted the products with dichloromethane (2×10 mL). The combined organic extracts were washed with water, dried (Na₂SO₄) and concentrated to dryness. The residue was dissolved in ethanol (0.5 mL), added 1N NaoH (0.5 mL) and stirred at room temperature for 1 h. The resulting solution was diluted with water (15 mL), and extracted with dichloromethane (2×10 mL). The combined dichloromethane extracts were washed with water, dried (Na₂SO₄) and concentrated to dryness. The residue was purified by flash chromatography (1% MeOH in EtOAc) to afford the title compound (0.032 g, 30%) as a white amorphous powder: ¹H NMR (CDCl₃/400 Hz) δ 7.45 (m, 2H), 7.18 (m, 1H), 7.05 (m, 3H), 6.23 (s, 1H), 5.24 (s, 2H), 4.56 (d, 2H, J=6.4 Hz), 4.08 (d, 2H, J=5.2 Hz), 2.79 (t, 1H), and 2.08 (s, 3H;) ¹⁹F NMR (CDCl₃/400 MHz) δ −111.88 (m) and −118.62 (m); ES-HRMS m/z 511.0482 (M+H C₂₂H₁₉N₂O₄F₃Br requires 511.0475).

Example 382

Preparation of ethyl 2-({[3-chloro-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

To solution of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-chloro-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate (0.3 g, 0.00057 mol) in dimethylacetamide (3.0 mL) was added N-methymorpholine (0.064 g, 0.00064 mol), followed by addition of ethylchloroformate (0.06 mL) and stirred at −10° C., for 30 min. The solvents were distilled in vacuo and the residue was purified by reverse-phase HPLC purification using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=481 M+H) were combined and freeze-dried, and the residue was partitioned between 5% sod. bicarbonate (20 mL) and dichloromethane (20 mL). The organic phase was washed with water, dried (Na₂SO₄) and concentrated to dryness under reduced pressure, to afford the title compound as a white amorphous powder (0.15 g, 55%): ¹H NMR (CD₃OD/400 MHz) δ 7.61 (m, 1H), 7.52 (m, 1H), 7.26 (t, 2H, J=8.4 Hz), 7.12 (dd, 1H), 7.05 (3d, 1H, J=2.4 Hz), 6.74 (s, 1H), 5.40 (s, 2H), 4.42 (s, 2H), 4.05 (q, 2H, J=7.2 Hz), 2.12 (s, 3H), and 1.21 (t, 3H, J=7.2 Hz); ES-HRMS m/z 481.1118 (M+H C₂₃H₂₁N₂O₄F₃Cl requires 481.1136).

Example 383

Preparation of isobutyl 2-({[3-chloro-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

The title compound was prepared by a procedure similar to the one described for Example 382. Yield 57%; ¹H NMR (CD₃OD/400 MHz) δ 7.61 (m, 1H), 7.51 (m, 1H), 7.24 (t, 2H, J=8.0 Hz), 7.18 (m, 1H), 7.06 (m, 1H), 6.74 (s, 1H), 5.40 (s, 2H), 4.21 (s, 2H), 3.79 (d. 2H, J=6.8 Hz), 2.12 (s, 3H), 1.85 (m, 1H), and 0.91 (d, 6H, J=6.4 Hz); ES-HRMS m/z 509.1422 (M+H C₂₅H₂₅N₂O₄F₃Cl requires 509.1449).

Example 384

Preparation of cyclopropylmethyl 2-({[3-chloro-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

The title compound was prepared by a procedure similar to the one described for Example 382. Yield 46%; ¹H NMR (CD₃OD/400 Hz) δ 7.61 (m, 1H), 7.55 (m, 1H), 7.24 (t, 2H, J=7.6 Hz), 7.18 (m, 1H), 7.05 (m, 1H), 6.73 (s, 1H), 5.40 (s, 2H), 4.42 (s, 2H), 3.83 (d, 2H, J=7.2 Hz), 2.12 (s, 3H), 1.1 (br, 1H), 0.58 (d, 2H), and 0.22 (d, 2H); ES-HRMS m/z 507.1316 (M+H C₂₅H₂₃N₂O₄F₃Cl requires 507.1293).

Example 385

Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate

Step 1. Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 4-hydroxy-6-methyl-2-pyrone (0.9 g, 0.007 mol) and 4-amino-5-aminomethyl-2-methylpyrimidine (1.0 g, 0.007 mol) in water (10.0 ml) was heated at 100° C. for 1 h under argon atmosphere. The reaction mixture was cooled, and filtered the yellow precipitate. It was washed successively with cold water, ethanol, and dried in vacuo to afford the title compound (1.01 g, 51%) as a pale yellow powder: ¹H NMR (DMSO-d_6/400 MHz) δ 7.62 (s, 1H), 7.04 (s, 1H), 5.83 (d, 1H, J=2.0 Hz), 5.58 (d, 1H, J=2.0 Hz), 4.92 (s, 2H), 2.24 (s, 3H), and 2.22 (s, 3H); ES-HRMS m/z 325.0304 (M+H C₁₂H₁₄N₄O₂Br requires 325.0295).

Step 2. Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-hydroxy-6-methylpyridin-2(1H)-one A mixture of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-hydroxy-6-methylpyridin-2(1H)-one (0.5 g, 0.002 mol), and NBS (0.4 g, 0.002 mol) in glacial acetic acid (5.0 ml) was stirred at room temperature for 1 h under argon atmosphere. Acetic acid was removed in vacuo, residue was triturated with EtOAc containing 10% EtOH, and filtered. The pale yellow precipitate was washed with EtOAc containing 10% EtOH and dried in vacuo to afford the title compound (0.47 g, 725) as a pale yellow powder: ¹H NMR (CD₃OD/400 MHz) δ 7.62 (s, 1H), 6.09 (s, 1H), 5.15 (s, 2H), 2.42 (s, 3H), and 2.33 (s, 3H); ES-HRMS m/z 247.1160 (M+H C₁₂H₁₅N₄O₂ requires 247.1190).

Step 3. Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate. To suspension of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-hydroxy-6-methylpyridin-2(1H)-one (1.0 g, 0.0031 mol) and potassium carbonate (0.004 mol) in dimethylacetamide (10.0 mL) was added 2,4 difluorobenzyl bromide (0.62 mL, 0.0048 mol) and stirred at room temperature for 2 hours. Dimethylacetamide was distilled in vacuo and the residue was purified by reverse-phase HPLC using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=566) were combined and freeze dried to afford 0.65 g (37%) of the title compound as its trifluoroacetate salt: ¹H NMR (CD₃OD/400 MHz) δ 7.65 (s, 1H), 7.58 (m, 1H), 7.05 (m, 2H), 6.61 (s, 1H), 5.31 (s, 2H), 5.18 (s, 2H), 2.51 (s. 3H), and 2.46 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.39 (m) and −115.98 (m); ES-HRMS m/z 451.0590 (M+H C₁₉H₁₈N₄O₂BrF₂ requires 451.0576).

Example 386

Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Hydrochloride

Ion exchange (25 g) BioRad AG 2X8 resin (200-400 mesh chloride form) was washed with 1M HCl (150 mL), and equilibrated for 2.5 h. This resin was loaded onto a column, and added a solution of Example 385 (3.3 g, 5.8 mmol) in water/CH₃CN (1:1). The column was eluted slowly over 1 h, fractions were collected, and freeze dried to afford the desired HCl salt (2.2 g, 72%) as a white solid: ¹H-NMR (CD₃OD, 400 Hz) δ 7.60 (m, 2H), 7.21 (m, 2H), 6.62 (s, 1H), 5.31 (s, 2H), 5.18 (s, 2H), 2.52 (s, 3H), 2.47 (s, 3H); ES-HRMS m/z 451.0544/453.0577 (M+H C₁₉H₁₇N₄O₂F₂Br requires 451.0581/453.0563).

Example 387

Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Trifluoroacetate

Step 1. Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-chloro-4-hydroxy-6-methylpyridin-2(1H)-one ¹H NMR (CD₃OD, 400 Hz) δ 7.62 (m, 1H), 6.11 (s, 1H), 5.13 (s, 2H), 2.66 (s, 3H), 2.42 (s, 3H); ES-HRMS m/z 281.0793 (M+H C₁₂H₁₃N₄O₂Cl requires 281.0800).

Step 2. Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate. The title compound was prepared from the product of Step 1 by a procedure similar to the one described for Example 385, step 2. ¹H NMR (CD₃OD, 400 Hz) δ 7.59 (m, 2H), 7.03 (m, 2H), 6.63 (s, 1H), 5.31 (s, 2H), 5.17 (s, 2H), 2.48 (s, 3H), 2.46 (s, 3H); ES-HRMS m/z 407.1097 (M+H C₁₉H₁₇N₄O₂ClF₂ requires 407.1081).

Example 388

Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Hydrochloride

Ion exchange (12.5 g) BioRad AG 2X8 resin (200-400 mesh chloride form) was washed with 1M HCl (150 mL), and equilibrated for 2.5 h. This resin was loaded onto a column, and added a solution of Example 387 (1.2 g, 2.4 mmol) in water/CH₃CN (1:1). The column was eluted slowly over 1 h, fractions were collected, and freeze dried to afford the desired HCl salt (1.03 g, 97%) as a white solid: ¹H NMR (CD₃OD, 400 Hz) δ 7.60 (m, 2H), 7.04 (m, 2H), 6.64 (s, 1H), 5.31 (s, 2H), 5.17 (s, 2H), 2.50 (s, 3H), 2.47 (s, 3H); ES-HRMS m/z 407.1079 (M+H C₁₉H₁₇N₄O₂ClF₂ requires 407.1081).

Example 389

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(1H-indazol-5-ylmethyl)-6-methylpyridin-2(1H)-one Trifluoroacetate

To a mixture of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.55 g, 0.0017 mol) and 5-(bromomethyl)-1-tetrahydro-2H-pyran-2-yl-1H-indazole (0.5 g, 0.0017 mol) in THF (10.0 mL) was added NaH (0.045 g, 0.0019 mol) and heated at 60° C. for 16 h under argon atmosphere. THF was distilled under reduced pressure, and the residue was suspended in EtOAc, added acetic acid (0.5 mL) and the product was purified by flash chromatography (80% EtOAc in hexane). The appropriate fractions were combined and concentrated to give an amorphous substance (0.31 g). This was stirred with trifluoroacetic (0.5 mL) for 30 min, the solution was diluted with acetonitrile (5 mL) and the product was isolated by reverse-phase HPLC using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=460) were combined and freeze dried to afford 0.14 g (52%) of the title compound as its trifluoroacetate salt: ¹H NMR (CD₃OD/400 MHz) δ 7.97 (s, 1H), 7.62 (m, 1H), 7.51 (m, 1H), 7.45 (s, 1H), 7.25 (m, 1H), 7.03 (t, 2H), 6.49 (s, 1H), 5.53 (s, 2H), 5.29 (s, 2H), and 2.40 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.69 (m), −116.09 (m); ES-HRMS m/z 460.0432 (M+H C₂₁H₁₇N₃O₂BrF₂ requires 460.0467).

Example 390

Preparation of N˜1˜-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-methylpyrimidin-4-yl)glycinamide Trifluoroacetate

To a solution of BOC-Gly-OH (0.19 g, 0.0011 mol) in DMF (2.0 mL), was added N-methylmorpholine (0.14 mL, 0.0011 mol), followed by the addition of isobutylchloroformate (0.15 mL, 0.0011 mol) and stirred at −10° C. for 15 min. Then added a solution of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate (0/125 g, 0.00022 mol) in DMF (2.0 mL) containing diisopropylethylamine (0.1 g, 0.006 mL) and the resulting mixture was stirred for 16 h, at room temperature. The solvents were distilled in vacuo and the residue was purified by by reverse-phase HPLC using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=608/610) were combined and freeze dried to afford 0.025 g of white powder. This was stirred with trifluoroacetic acid (0.5 mL) for 1 h and product was isolated by reverse-phase HPLC using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=508/510) were combined and freeze dried to afford the title compound (0.02 g) as a white powder: ¹H NMR (CD₃OD/400 MHz) δ 8.18 (s, 1H), 7.61 (m, 1H), 7.02 (m, 2H), 6.59 (s, 1H), 5.30 (s, 4H), 4.23 (s, 2H), 2.60 (s, 3H), and 2.47 (s, 3H); ES-HRMS m/z 508.0797 (M+H C₂₁H₂₁N₅O₃BrF₂ requires 508.0790).

Example 391

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-4-yl]methyl}pyridin-2(1H)-one

Step 1. Preparation of 4-(bromomethyl)-2-(methylthio)pyrimidine To a solution of 4-methyl-2-methylthiopyrimidine (12.6 g, 0.09 mol) in acetic acid (50.0 mL) was added bromine (5.5 mL, 0.11 mol) and heated at 80° C. under argon atmosphere for 2 h. Acetic acid was distilled in vacuo, the residue was triturated with dichloromethane (100.0 mL) and poured into satd. sod. bicarbonate solution (200.0 mL). Additional dichloromethane (100.0 ml) was added and stirred for 15 min. The organic phase was washed with water (3×100 mL), dried (Na₂SO₄), and concentrated under reduced pressure. The dark colored residue was purified by flash chromatography (EtOAc/hexane 1:4 v/v) to afford 4-(bromomethyl)-2-(methylthio)pyrimidine (10.9 g, 55%) as a dark colored liquid: ¹H NMR (CDCl₃/400 MHz) δ 8.50 (d, 1H, J=4.8 Hz), 7.09 (d, 1H, J=4.8 Hz), 4.34 (s, 2H), and 2.56 (s, 3H); ESMS m/z 219 (M+H).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-4-yl]methyl}pyridin-2(1H)-one. To a mixture of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one 5.0 g, 0.015 mol) and 4-(Bromomethyl)-2-(methylthio)pyrimidine (4.0 g, 0.018 mol) in THF (50.0 mL) was added NaH (0.4 g, 0.0017) and stirred at 55° C. under argon for 16 h. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between 5% citric acid (25 mL) and EtOAc (50 mL). A precipitate was formed, it was filtered, washed with water, EtOAc, and dried in vacuo to afford the title compound (4.2 g, 59%) as a light brown powder, ¹H NMR (CD₃OD/400 MHz) δ (8.45 (d, 1H, J=5.2 Hz), 7.6 (m, 1H), 7.06 (d over m, 2H, J=5.2 Hz), 6.54 (s, 1H), 5.39 (s, 2H), 5.32 (s, 2H), 2.43 (s, 3H), 2.33 (s, 3H); ES-HRMS m/z 468.0173 (M+H C₁₉H₁₇N₃O₂BrSF₂ requires 468.0187).

Example 392

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-4-yl]methyl}pyridin-2(1H)-one

A suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-4-yl]methyl}pyridin-2(1H)-one 0.28 g, 0.0006 mol), and magnesium monoperoxyphthalate hexahydrate 90.6 g, 0.0012 mol) in acetonitrile (8.0 ml) and water (2.0 ml) was stirred at room temperature for 16 h. The resulting clear solution was concentrated under reduced pressure, and the residue was partitioned between dichloromethane (30 mL) and water (20 mL). The organic phase was washed with water, dried (Na₂SO₄) and concentrated to afford the title compound (0.27 g, 90%) as a pale yellow substance: ¹H NMR (CD₃OD/400 MHz) δ 8.91 (d, 1H, J=5.2 Hz), 7.63 (d over m, 2H, J=5.2 Hz), 7.03 (m, 2H), 6.58 (s, 1H), 5.54 (s, 2H), 5.33 (s, 2H), 3.28 (s, 3H), and 2.49 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.58 (m), −115.98 (m) □ ES-HRMS m/z 500.0113 (M+H C₁₉H₁₇N₃O₄BrSF₂ requires 500.0086).

Example 393

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile Trifluoroacetate

A mixture of 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-4-yl]methyl}pyridin-2(1H)-one (1.0 g, 0.002 mol) and NaCN (0.15 g, 0.0031 mol) in DMF (5.0 mL) was stirred at room temperature for 2 h under argon atmosphere. DMF was distilled in vacuo, the residue was triturated with acetonitrile (10 mL) and water (10 mL), and filtered the red colored precipitate. It was washed with acetonitrile and dried to afford the title compound (0.26 g). The washings and the fitrate were combined and purified by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min) at a flow rate of 100 ml/min to give an additional 0.5 g of the title compound: ¹H NMR (CD₃OD/400 MHz) δ 8.83 (d, 1H, J=5.2 Hz), 7.62 (d over m, 2H, J=5.2 Hz), 7.00 (m, 2H), 6.58 (s, 1H), 5.46 (s, 2H), 5.33 (s, 2H), and 2.47 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.64 (m), −116.03 (m); ES-HRMS m/z 447.0278 (M+H C₁₉H₁₄N₄O₂BrF₂ requires 447.0263).

Example 394

Preparation of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one Trifluoroacetate

To a solution of 4-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile trifluoroacetate (0.3 g. 0.00066 mol) in a solvent mixture of EtOAc (15.0 mL) and acetic acid (5.0 mL), was added Pd/C (10%, 0.18 g) and stirred in an atmosphere of hydrogen at 15 psi for 2 h. The catalyst was removed by filtration. The filtrate was concentrated to dryness and the residue was residue was purified by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min) at a flow rate of 100 ml/min. The appropriate fractions (m/z=451) were combined and freeze dried to afford (0.32 g, 645) of the title compound as its trifluoroacetate salt: ¹H NMR (DMSO-d₆/400 MHz) δ 8.78 (d, 1H, J=5.2 Hz), 8.28 (br, 2H), 7.62 (m, 1H), 7.38 (m, 1H), 7.25 (d, 1H, J=5.2 Hz), 7.18 (m 1H), 6.62 (s, 1H), 5.32 (s, 2H), 5.29 (s, 2H), 4.24 (s, 2H), and 2.46 (s, 3H); ¹⁹F NMR (DMSO-d₆/400 MHz) δ −109.59 (m), −113.67 (m); ES-HRMS m/z 451.0530 (M+H C₁₉H₁₈N₄O₂BrF₂ requires 451.0576).

Example 395

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-methoxypyrimidin-4-yl)methyl]-6-methylpyridin-2(1H)-one Trifluoroacetate

A solution of 4-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile trifluoroacetate (0.13 g, 0.00023 mol) in MeOH (2.0 mL) was treated with 1N NaOH (0.5 mL). After stirring at room temperature for 3 h, it was heated at 60° C. for an additional 3 h and left overnight room temperature. The resulting solution was diluted with acetonitrile, and purified by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min) at a flow rate of 100 mL/min. The appropriate fractions (m/z=452) were combined and freeze dried to afford the title compound (0.015 g) as a white powder: ¹H NMR (CD₃OD) δ 8.84 (d, 1H, J=5.2 Hz) 7.62 (d, 1H, J=5.2 Hz), 7.05 (m, 2H), 6.57 (s, 1H), 5.49 (s, 2H), 5.32 (s, 2H), 3.96 (s, 3H), and 2.49 (s, 3H); ES-HRMS m/z 452.0440 (M+H C₁₉H₁₇N₃O₃BrF₂ requires 452.0416).

Example 396

Preparation of Methyl 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carboxylate Trifluoroacetate

The title compound was obtained as a second product in the formation of 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-methoxypyrimidin-4-yl)methyl]-6-methylpyridin-2(1H)-one trifluoroacetate. ¹H NMR (CD₃OD/400 MHz) δ 8.46 (d, 1H, J=5.2 Hz), 7.62 (m, 1H), 7.00 (m 2H), 6.93 (d, 1H, J=5.2 Hz), 6.55 (s, 1H), 5.39 (s, 2H), 5.32 (s, 2H), 3.85 (s, 3H), and 2.44 (s, 3H); ES-HRMS m/z 480.0340 (M+H C₂₀H₁₇N₃O₄BrF₂ requires 480.0365).

Example 397

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-hydroxypyrimidin-4-yl)methyl]-6-methylpyridin-2(1H)-one Trifluoroacetate

A mixture of 4-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile trifluoroacetate (0.2 g, 0.00035 mol) potassium fluoride on aluminum oxide (0.25 g) in t-butanol (5.0 mL) was refluxed for 4 h under argon atmosphere. The reaction mixture was cooled, filtered the precipitate and washed with ethanol. The combined filtrate and washings were concentrated to dryness and the residue was purified by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min) at a flow rate of 100 ml/min. The appropriate fractions (m/z=452) were combined and freeze dried to afford the title compound (0.05 g) as a white powder: ¹H NMR (DMSO-d₆/400 Mz) δ 8.75 (d, 1H J=6.4 Hz), 7.64 (m, 1H), 7.30 (m 1H), 7.15 (m 1H), 6.55 (s, 1H), 6.22 (d, 1H, J=6.4 Hz), 5.28 (s, 2H), 5.12 (d, 2H), and 2.29 (s, 3H); ¹⁹F-NMR (DMSO-d₆/400 MHz) δ −109.69 (m), and −113.67 (m); ES-HRMS m/z 438.0228 (M+H C₁₈H₁₅N₃O₃BrF₂ requires 438.0259).

Example 398

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carboxamide Trifluoroacetate

The title compound was obtained by a procedure described for Example 397. ¹H NMR (DMSO-d₆/400 MHz) δ 8.82 (d, 1H J=5.2 Hz), 8.01 (br, 1H), 7.79 (br 1H), 7.64 (m, 1H), 7.34 (m, 2H), 7.16 (m 1H), 6.62 (s, 1H), 5.36 (s, 2H), 5.30 (s, 2H), and 2.38 (s, 3H); ¹⁹F NMR (DMSO-d₆/400 MHz) δ −109.64 (m), and −113.66 (m); ES-HRMS m/z 465.0385 (M+H C₁₉H₁₆N₄O₃BrF₂ requires 465.0368).

Example 399

Preparation of Methyl (4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)methylcarbamate

To a solution of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate (0.13 g, 0.00023 mol) in dimethylacetamide (1.0 mL), was added triethylamine (0.04 mL, 0.0003 mol), followed by the addition of methylchloroformate (0.05 mL) and stirred at 0° C. for 30 min under argon atmosphere. The reaction mixture was diluted with water (10 mL) and extracted with EtOAc (2×20 mL), The combined organic extracts were washed with water, dried (Na₂SO₄) and concentrated to dryness. The resulting residue was purified by flash chromatography (5% MeOH in EtOAc) to afford the title compound (0.055 g, 37%) as pale yellow powder: ¹H NMR (DMSO-d₆/400 MHz) δ 8.65 (d, 1H J=5.6 Hz), 7.63 (1H), 7.5 (m, 1H), 7.28 (m 1H), 7.13 (m, 2H), 6.59 (s, 1H), 5.28 (s, 4H), 5.26 (d, 2H, J=6.0 Hz), and 2.46 (s, 3H); ¹⁹F NMR (DMSO-d₆/400 MHz) δ −109.64 (m), and −113.71 (m); ES-HRMS m/z 509.0621 (M+H C₂₁H₂₀N₄O₄BrF₂ requires 509.0630).

Example 400

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one

Step 1. Preparation of 4-hydroxy-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one A mixture of 4-hydroxy-6-methyl-2-pyrone (5.0 g, 0.04 mol) and 5-aminomethyl-2-methylpyrazine (5.0 g, 0.041 mol) in water (25.0 ml) was heated at 100° C. for 1 h under argon atmosphere. The reaction mixture was cooled, and filtered the yellow precipitate. It was washed with ethanol, and dried in vacuo to afford the title compound (5.8 g, 63%) as a pale yellow powder: ¹H NMR (DMSO-d₆/400 MHz) δ 10.43 (br, 1H), 8.38(d, 2H, J=5.2 Hz), 5.77 (d, 1H, J=2.0 Hz), 5.58 (d, 1H, J=2.0 Hz), 4.92 (s, 2H), 2.24 (s, 3H), and 2.22 (s, 3H); ESMS m/z 232 (M+H).

Step 2. Preparation of 3-bromo-4-hydroxy-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one The title compound was prepared by a procedure described in step 2 for Example 385. Yield: 64%, 1H NMR (CD₃OD/400 MHz) δ 8.47 (s, 1H), 8.42 (s, 1H), 6.07 (s, 1H), 5.38 (s, 2H), 2.51 (s, 3H), and 2.44 (s, 3H), ESMS m/z 310 and 312 (M+H).

Step 3. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one. To a mixture of 3-Bromo-4-hydroxy-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one (0.45 g, 0.0015 mol), and potassium carbonate (0.25 g, 0.0018 mol) in dimethylacetamide (5.0 mL) was added 2,4 difluorobenzyl bromide (0.25 mL. 0.0019 mol) and stirred at room temperature under argon for 1 h. Dimethylacetamide was distilled in vacuo and the residue was partitioned between CH₂Cl₂ (20 mL) and water (20 mL). The organic phase was washed with water, dried (Na₂SO₄) and concentrated under reduced pressure. The resulting material was purified by flash chromatography (EtOAc/hexane 4:1 v/v) as the eluent. The appropriate fractions (m/z=451/453) were combined and concentrated under reduced pressure to give a white (0.25 g, 38%) solid. ¹H NMR (CD₃OD/400 MHz) δ 8.49 (s, 1H), 8.40 (s, 1H), 7.60 (m, 1H), 6.99 (m, 2H), 6.51 (s, 1H), 5.42 (s, 2H), 5.29 (s, 2H), 2.54 (s, 3H), and 2.50 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −117.70 (m) and −116.09 (m); ES-HRMS m/z 436.0439 (M+H C₁₉H₁₇N₃O₂BrF₂ requires 436.0467).

Example 401

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyrazin-2-ylmethyl)pyridin-2(1H)-one

Step 1. Preparation of 2-chloromethylpyrazine A mixture of 2-methylpyrazine (3.5 g, 0.037 mol), NCS (6.3 g, 0.047 mol) and benzoyl peroxide (0.05 g) was heated to reflux for 16 h under argon atmosphere. It was filtered and the filtrate was concentrated to dryness. The resulting residue was purified by flash chromatography using 30% EtOAc in hexane to afford 2-chloromethylpyrazine as a dark colored liquid (1.7 g, 36 5): ¹H NMR (CD₃OD/400 MHz) δ 8.75 (d, 1H, J=1.2 Hz), 8.58 (m, 1H), 8.56 (m, 1H), and 4.75 (s, 2H); ESMS m/z=129 (M+H).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyrazin-2-ylmethyl)pyridin-2(1H)-one. 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (1.8 g, 0.0055 mol) and 2-chloropyrazine (0.8 g, 0.00625) were suspended in THF (25 mL), then added NaH (0.15 g, 0.0062 mol), KI (0.1 g) and the mixture was heated at 65° C. under argon atmosphere for 16 h. The reaction mixture was cooled, added acetic acid (0.5 mL) and concentrated to dryness under reduced pressure. The residue was stirred with a mixture of water (50 mL) and EtoAc (25 mL) and filtered the precipitate. It was washed with water, and acetonitrile an dried in vacuo to afford 1.7 g of light brown powder. ¹H NMR (CD₃OD/400 MHz) δ 8.65 (d, 1H), 8.49 (m, 1H), 8.47 9 m, 1H), 7.61 (q, 1H), 7.02 (m, 2H), 6.52 (s, 1H), 5.47 (s, 2H), 5.23 (s, 2H), and 2.53 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.72 (m) and −116.07 (m); ES-HRMS m/z 422.0283 (M+H C₁₈H₁₅N₃O₂BrF₂ requires 422.0310).

Example 402

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one

Step 1. Preparation of ethyl 5-methylpyrazine-2-carboxylate A solution of 5-methylpyrazine-2-carboxylic acid (15.0 g, 0.109 mol) in ethanol (70.0 mL) containing (1.5 g, 0.0079 mol) was heated to reflux for 4 h under argon atmosphere. The dark colored solution was cooled, added sod. bicarbonate (1.0 g) and concentrated under reduced pressure. The residue was partitioned between water (50 mL) and EtOAc (100 mL). The organic layer was washed with water (2×25 mL), dried (Na₂SO₄), and concentrated under reduced pressure to afford ethyl 5-methylpyrazine-2-carboxylate (12.05 g, 67%) as an orange colored liquid: ¹H NMR (CD₃OD/400 MHz) δ 9.1 (d, 1H, J=1.2 Hz), 8.62 (d, 1H, J=1.2 Hz), 4.45 (q, 2H, J=7.2 Hz), 2.63 (s, 3H), and 1.41 (t, 3H, J=7.2 Hz); ESMS m/z 167 (M+H).

Step 2. Preparation of ethyl 5-(bromomethyl)pyrazine-2-carboxylate A solution of ethyl 5-methylpyrazine-2-carboxylate (12.0 g, 0.072 mol) in glacial acetic acid (60 mL) containing bromine (4.0 mL) was heated at 80° C. under anhydrous conditions for 45 min. After the removal of acetic acid in vacuo, the residue was partitioned between saturated, bicarbonate (100 mL) and EtOAc (3×30 mL). The combined EtOAc extracts were washed with water (2×25 mL), dried (Na₂SO₄), and concentrated under reduced pressure. The resulting liquid was purified by flash chromatography (20% EtOAc in hexane) to afford ethyl-(5bromomethylpyrazine-2-carboxylate (7.7 g, 44%) as an orange colored liquid: ¹H NMR (CD₃OD/400 MHz) δ 9.18 (d, 1H, J=1.2 Hz), 8.85 (d, 1H, J=1.2 Hz), 4.71 (d, 2H), 4.47 (q, 2H, J=7.2 Hz), and 1.42 (t, 3H, J=7.2 Hz); ES-HRMS m/z 244.9942 (M+H C₈H₁₀N₂O₂Br requires 244.9920).

Step 3. Ethyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate To a mixture of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (6.0 g, 0.018 mol) and ethyl 5-(bromomethyl)pyrazine-2-carboxylate (4.9 g, 0.02 mol) in THF (50.0 mL) was added NaH (0.5 g) and heated at 55° C. under argon atmosphere for 3 h. The reaction mixture was cooled, added acetic acid (1.2 ml) and concentrated under reduced pressure. The residue was triturated with water and filtered the solid. It was washed with water, followed by ethanol and dried in vacuo to afford the title compound (3.0 g, 78%) as alight brown powder: ¹H NMR (CD₃OD/400 MHz) δ 9.10 (d, 1H, J=1.2 Hz), 8.77 (d, 1H, J=1.2 Hz), 7.61 (m, 1H), 7.01 (m 2H), 6.54 (s, 1H), 5.54 (s, 2H), 5.30 (s, 2H), 4.43 (q, 2H, J=6.8 Hz), 2.52 (s, 3H), and 1.39 (t, 3H, J=6.8 Hz); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.64 (m) and −116.04 (m); ES-HRMS m/z 494.0482 (M+H C₂₁H₁₉N₃O₄BrF₂ requires 494.0522).

Step 4. 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one. To a suspension of ethyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate (2.0 g, 0.004 mol) in t-butanol (15.0 mL and THF (5.0 mL) was added NaBH₄ (0.18 g, 0.0047 mol) and the mixture was stirred at room temperature for 16 h under argon atmosphere. It was cooled, added MeOH (5.0 mL) and acetic acid (1.0 mL) and concentrated to dryness. The residue was triturated with water and filtered. It was washed with water, dried in vacuo and purified by flash chromatography (1% MeOH in EtOAc to afford the title compound (0.75 g, 41%) as a pale yellow powder: ¹H NMR (CD₃OD/400 MHz) δ 8.58 (d, 1H, J=1.6 Hz), 8.56 (d, 1H, J=1.6 Hz), 7.6 (m, 1H), 7.01 (m, 2H), 6.52 (s, 1H), 5.46 (s, 2H), 5.29 (s, 2H), 4.71 (s, 2H), and 2.54 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.70 (m) and −116.06 (m); ES-HRMS m/z 452.0394 (M+H C₁₉H₁₇N₃O₃BrF₂ requires 452.0416).

Example 403

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-({5-[(dimethylamino)methyl]pyrazin-2-yl}methyl)-6-methylpyridin-2(1H)-one Trifluoroacetate

Step 1. Preparation of 3-bromo-1-{[5-(Chloromethyl)pyrazin-2-yl]methyl}-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Cyanurylchloride (0.42 g, 0.0023 mol) was added to DMF (0.52 mL) and stirred at room temperature for 15 min. Then added dichloromethane (15 mL) followed by the addition of 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one 1.0 g, 0.0022 mol) and reaction mixture was stirred at room temperature under argon atmosphere. After 1 h, an additional 1.0 mL of DMF was added and the reaction was allowed to proceed for another hour, when a clear solution was obtained. The solution was diluted with dichloromethane (20 mL) and washed with water, dried (Na₂SO₄), and concentrated to dryness under reduced pressure. The residue was triturated with EtOAc, filtered, washed with EtOAc and dried to afford 0.79 g (77%) of the title compound as a pale yellow powder: ¹H NMR (CD₃OD/400 MHz) δ 8.66 (s, 2H), 7.73 (m, 1H), 7.05 (m, 2H), 6.56 (s, 1H), 5.52 (s, 2H), 5.33 (s, 2H), 4.74 (s, 2H), and 2.57 (s, 3H); ES-HRMS m/z 470.0051 (M+H C₁₉H₁₆N₃O₂BrClF₂ requires 470.0077).

Step 2. Preparation of 3-bromo-1-{[5—(Chloromethyl)pyrazin-2-yl]methyl}-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one A suspension of 3-bromo-1-{[5-(chloromethyl)pyrazin-2-yl]methyl}-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.25 g, 0.00053 mol) in THF (1.0 mL) was treated with N, N,-dimethyl amine (1.0 mL of 2M soln in THF) and stirred at room temperature for 16 h. The reaction mixture was concentrated and the title compound was isolated by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min) at a flow rate of 100 ml/min. The appropriate fractions (m/z=479) were combined and freeze dried to afford the title compound (0.27 g, 87%) as a white powder: ¹H NMR (CD₃OD/400 MHz) δ 8.78 (d, 1H), 8.56 (d, 1H, J=1.2 Hz), 7.61 (m 1H), 7.01 (m, 2H), 6.55 (s, 1H), 5.49 (s, 2H), 5.30 (s, 2H), 4.52 (s, 2H), 2.94 (s, 6H) and 2.57 (s, 3H); ¹⁹F NMR (CD₃OD) δ −111.56 (m) and −116.02 (m); ES-HRMS m/z 479.0885 (M+H C₂₁H₂₂N₄O₂BrF₂ requires 479.0889).

Example 404

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(5-{[(2-hydroxyethyl)(methyl)amino]-methyl}pyrazin-2-yl)methyl]-6-methylpyridin-2(1H)-one Trifluoroacetate

The title compound was prepared in a similar manner as described for Example 403, substituting N-methylaminoethanol for N, N-dimethylamine. Yield=78%, ¹H NMR (CD₃OD/400 MHz) δ 8.78 (d, 1H), 8.59 (d. 1H, J=1.2 Hz), 7.6 (m, 1H), 7.01 (m, 2H), 6.55 (s, 1H), 5.49 (s, 2H), 5.30 (s, 2H), 3.89 (t, 2H), 2.97 (s, 3H), and 2.57 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.56 (m) and −116.04 (m); ES-HRMS m/z 509.0964 (M+H C₂₂H₂₄N₄O₃BrF₂ requires 509.0994).

Example 405

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(4-methylpiperazin-1-yl)carbonyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one Trifluoroacetate

Step 1. Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylic acid A suspension of ethyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate (0.18 g, 0.002 mol) and 1N NaOH (0.6 mL in 1:1 v/v EtOH/Water) was stirred at room temperature for 1.5 h. The reaction mixture was acidified with 5% citric acid and filtered the precipitate. It was washed with water, followed by ethanol and dried in vacuo to afford the title compound (0.14 g, 77%) as a light brown powder: ¹H NMR (CD₃OD/400 MHz) δ 9.03 (s, 1H), 8.60 (s, 1H), 7.61 (m. 1H), 7.00 (m, 2H), 6.52 (s, 1H), 5.51 (s, 2H), 5.30 (s. 2H), and 2.52 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.75 (m) and −116.06 (m); ES-HRMS m/z 466.0209 (M+H C₁₉H₁₅N₄O₃BrF₂ requires 466.0209).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(4-methylpiperazin-1-yl)carbonyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one trifluoroacetate. To a solution of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylic acid (0.28 g, 0.0006 mol) in DMF (3.0 mL), at −15° C., was added isobutylchloroformate (0.082 g, 0.0006 mol), followed by the addition of N-methylmorpholine (0.06 g, 0.00063 mol) and stirred under argon for 15 min. N-methylpiperazine (0.072 g, 0.00072 mol) in DMF (2.0 mL) was then added to the reaction and the mixture was stirred at room temperature for 3 h. After the removal of the solvents in vacuo, the residue was purified by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min) at a flow rate of 100 ml/min. The appropriate fractions (m/z=548) were combined and freeze dried to afford the title compound (0.32 g, 80%) as a white powder: ¹H NMR (CD₃OD/400 MHz) δ 8.89 (d, 1H, J=1.6 Hz), 8.73 (d, 1H, J=1.6 Hz), 7.61 (m, 1H), 7.01 (m, 2H), 6.56 (s, 1H), 5.50 (s, 2H), 5.30 (s, 2H), 2.9 (s, 3H), and 2.57 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz)=6-109.36 (m) and −114.91 (m); ES-HRMS m/z 548.1090 (M+H C₂₄H₂₅N₅O₃BrF₂ requires 548.1103).

Example 406

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(4-methylpiperazin-1-yl)carbonyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one

A solution of 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(4-methylpiperazin-1-yl)carbonyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one trifluoroacetate (0.17 g, 0.00026 mol) in 0.1N NaOH (25 mL) was stirred at room temperature for 15 min. and extracted the product in ethyl acetate (2×20 mL). The combined organic extracts were washed with water (2×20 mL), dried (Na₂SO₄) and concentrated to dryness. The residue was dried in vacuo to afford the title product (0.09 g, 64%) as a white powder: ¹H NMR (CD₃OD/400 MHz) δ 8.69 (d, 1H, J=1.2 Hz), 8.67 (d, 1H, J=1.2 Hz), 7.60 (m, 1H), 7.00 (m, 2H), 6.54 (s, 1H), 5.50 (s, 2H), 5.30 (s, 2H), 3.78 (t, 2H, J=4.8 Hz), 3.58 (t, 2H, J=4.8 Hz), 2.526 (s, 3H), 2.53 (t, 2H, J=4.8 Hz), 2.44 (t, 2H, J=4.8 Hz), and 2.31 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −111.65 (m) and −116.06 (m); ES-HRMS m/z 548.1123 (M+H C₂₄H₂₅N₅O₃BrF₂ requires 548.1103).

Example 407

Preparation of 5-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)-N-methylpyrazine-2-carboxamide

The title compound was prepared in a similar manner as described for Example 405, substituting N-methylpiperazine by N-methylethanolamine. Yield=60%, ¹H NMR (CD₃OD/400 MHz) δ 8.69 (d, 1H, J=1.2 Hz), 8.64 (d. 1H, J=1.2 Hz), 7.61 (m, 1H), 7.00 (m, 2H), 6.54 (s, 1H), 5.49 (s. 2H), 5.30 (s, 2H), 3.81 (t, 1H), 3.66 (m, 2H), 3.56 (t, 1H, J=5.2 Hz), 3.12 (d, 3H J=7.6 Hz), 2.56 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −109.64 (m) and −113.66 (m); ES-HRMS m/z 523.0743 (M+H C₂₂H₂₂N₄O₄BrF₂ requires 523.0797).

Example 408

Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2,3-dihydroxypropyl)pyrazine-2-carboxamide

The title compound was prepared in a similar manner as described for EXAMPLE 405, substituting N-methylpiperazine by 3-amino-1,2-propanediol. Yield=56%; ¹H NMR (CD₃OD/400 MHz) δ 9.09 (d, 1H, J=1.2 Hz), 8.70 (d. 1H, J=1.2 Hz), 7.60 (m, 1H), 7.00 (m, 2H), 6.54 (s, 1H), 5.53 (s. 2H), 5.30 (s, 2H), 3.80 (m, 1H), 3.61 (dd, 1H), 5.53 (d, 2H), J=5.2 Hz), 3.42 (dd, 1H), and 2.55 (s, 3H); ¹⁹F NMR (CD₃OD/400 MHz) δ −109.65 (m) and −113.67 (m); ES-HRMS m/z 539.0703 (M+H C₂₂H₂₂N₄O₄BrF₂ requires 539.0736).

Example 409

Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)pyrazine-2-carboxamide

The title compound was prepared in a similar manner as described for EXAMPLE 405, substituting N-methylpiperazine by 2-aminoethanol. Yield=46%; ¹H NMR (CD₃OD/400 Hz) δ 9.08 (d, 1H, J=1.2 Hz), 8.70 (d, 1H, J=1.2 Hz), 7.601 (m, 1H), 7.01 (m, 2H), 6.54 (s, 1H), 5.53 (s, 2H), 5.30 (s, 2H), 3.69 (t, 2H, J=6.0 Hz), 3.53 (t, 2H, J=6.0 Hz), 2.55 (s, 3H); ¹⁹F NMR (CD₃OD/400 Hz) δ −111.67 (m) and −116.07 (m); ES-HRMS m/z 509.0616 (M+H C₂₁H₂₀N₄O₄BrF₂ requires 509.0630).

Example 410

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(methoxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one

To a solution of 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one (0.35 g, 0.00078 mol) in DMF at 0° C., was added NaH (0.022 g, 0.00092 mol) and stirred for 10 min. Iodomethane (0.05 mL) was added to the reaction and the mixture was stirred at 10° C. for 3 h. DMF was distilled in vacuo and the residue was partitioned between 5% citric acid and EtOAc (15.0 mL). The organic phase was washed with water, dried (Na₂SO₄) and concentrated to dryness. The residue was purified by flash chromatography (EtOAc), and the appropriate fractions were combined and concentrated to a pale yellow powder. ¹H NMR (CD₃OD/400 MHz) δ 8.59 (s), 8.55 (s, 1H), 7.60 (m, 1H), 6.99 (m, 2H), 6.52 (s, 1H), 5.47 (s, 2H), 5.30 (s, 2H), 4.57 (s, 2H), 3.44 (s, 2H), and 2.54 (s, 3H); ¹⁹F NMR (CD₃OD/400 Hz) δ −11.69 (m) and −116.09(m); ES-HRMS m/z 466.0577 (M+H C₂₁H₁₉N₃O₃BrF₂ requires 466.0572).

Example 411

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-({5-[(2-methoxyethoxy)methyl]pyrazin-2-yl}methyl)-6-methylpyridin-2(1H)-one

To a solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one (0.25 g, 0.00055 mol) in dimethyl acetamide at 0° C., was added NaH (0.016 g, 0.00067 mol) and stirred for 15 min. 2-Methoxyethyl bromide (0.09 g, 0.00-65 mol) was then added, and the mixture was stirred at room temperature for 6 h. Dimethylacetamide was distilled in vacuo and the product was purified by reverse-phase HPLC using 10-90% acetonitrile/water gradient (30 min) at a flow rate of 100 ml/min. The appropriate fractions (m/z=510) were combined and freeze dried to afford the title compound (0.32 g, 80%) as a white powder: ¹H NMR (CD₃OD/400 Hz) δ 8.59 (s, 1H), 8.58 (s, 1H), 7.60 (m, 1H), 7.02 (m, 2H), 6.52 (s, 1H), 5.45 (s, 2H), 5.29 (s, 2H), 4.67 (s, 2H), 3.71 (t, 2H,), 3.57 (t, 2H), 3.34 (s, 3H), and 2.54 (s, 3H); ES-HRMS m/z 510.0852 (M+H C₂₀H₁₈N₄O₄BrF₂ requires 510.0835).

Example 412

Preparation of (5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl Carbamate

To a suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one (0.21 g, 0.00055 mol) in THF (5.0 mL) and DMF (2.0 mL), was added 4-nitrophenylchloroformate (0.1 g, 0.0005 mol) and cooled to 0° C. Triethylamine (0.052 g, 0.0005 mol) was then added, stirred at room temperature for 1 h, and at 65° C. for an additional 1 h. It was cooled in an ice bath and added 2M ammonia in propanol (1.0 mL) and stirred at room temperature for 2 h. After the removal of the solvents under reduced pressure, the residue was partitioned between 5% sod. bicarbonate, and EtOAc (25 mL). The organic phase was washed with 5% sod. bicarbonate, (3×25 mL), water (3×25 mL), dried (Na₂SO₄) and concentrated under reduced pressure. The resulting substance was purified by isolated by reverse-phase HPLC using 10-90% CH₃CN/Water (30 min gradient) at a flow rate of 100 ml/min. The appropriate fractions (m/z=495 M+H) were combined and freeze-dried, and the residue was partitioned between 5% sod. bicarbonate (20 mL) and EtOAc (25 mL). The organic phase was washed with water, dried (Na₂SO₄) and concentrated to dryness under reduced pressure, to afford the title compound as a white powder (0.065 g): ¹H NMR (CD₃OD/400 MHz) δ 8.61 (s, 1H), 8.54 (br s, 1H), 7.60)m 1H), 7.02 (m, 2H), 6.52 (s, 1H), 5.47 (s, 2H), 5.29 (s, 2H), 5.15 (s, 2H), and 2.54 (s, 3H): ¹⁹F NMR (CD₃OD) δ −111.70 (m), and −116.09 (m); ES-HRMS m/z 495.0449 (M+H C₂₀H₁₈N₄O₄BrF₂ requires 495.0474).

Example 413

Preparation of 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl Methyl(phenyl)carbamate

Step 1. Preparation of 1-benzyl-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate To a chilled solution of 1-benzyl-4-hydroxypyridin-2(1H)-one (0.375 g, 1.86 mmol) in anhydrous acetonitrile (10 mL) was added triethylamine (0.206 g, 2.04 mmol) followed by N-methyl-N-phenylcarbamoyl chloride (0.379 g, 2.24 mmol). The reaction mixture was stirred under nitrogen atmosphere at 0° C. for 30 minutes then at room temperature for 1 hour. The reaction was monitored by TLC (5% methanol in dichloromethane). The solvent was removed under reduced pressure and the residue was washed with 10% citric acid and extracted with ethyl acetate. The organic extracts were combined, washed with water and dried over anhydrous Na₂SO₄. The solvent was removed under reduced pressure to afford a yellow syrup. The residue was purified by flash chromatography (silica gel) using 5% MeOH in CH₂Cl₂ to give the desired product (0.382 g, 61%) as a white semisolid. ¹H-NMR (d₆-DMSO, 400 MHz) δ 7.8 (d, 1H, J=7.2 Hz), 7.39 (m, 10H), 6.19 (s, 2H), 5.03 (s, 2H), 3.29 (s, 3H); ES-HRMS m/z 335.1396 (M+H calculated for C₂₀H₁₉N₂O₃ requires 335.1418).

Step 2. Preparation of 1-benzyl-3-bromo-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate To a solution of 1-benzyl-2-oxo-1,2-dihydropyridin-4-yl methyl(phenyl)carbamate (0.38 g, 1.13 mmol) in anhydrous CH₂Cl₂ (7 mL) was added N-bromosuccinimide (NBS, 0.24 g, 1.34 mmol). The reaction was stirred overnight at room temperature under nitrogen atmosphere. The reaction mixture was purified by flash chromatography (silica gel) using ethyl acetate/hexane (1:1 v/v). The appropriate fractions were collected according to ES MS (M+H 413) and concentrated. The dried product showed about 14% of di-bromonated product by analytical HPLC. The compounds were separated by reverse phase HPLC using a 10-90% acetonitrile in water (30 minute gradient) at a 100 ml/min flow rate to afford (after lyophilization) the salt of the desired compound. The salt was diluted in ethyl acetate and washed with NaHCO₃. The organic extracts were dried over anhydrous Na₂SO₄ and concentrated to afford the desired compound (0.271 g, 58%) as a beige solid. ¹H-NMR (d₆-DMSO, 400 MHz) δ 7.94 (d, 1H, J=7.2 Hz), 7.29 (m, 10H), 6.48 (s, 1H), 5.12 (s, 2H), 3.33 (s, 3H); ES-HRMS m/z 413.0495 (M+H calculated for C₂₀H₁₈O₃Br requires 413.0496).

Example 414

Preparation of 4-(benzyloxy)-3-ethynyl-1-(3-fluorobenzyl)pyridin-2(1H)-one

Step 1. Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one A mixture of 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one (4.83 g, 15.6 mmol) in anhydrous acetonitrile (55 mL) and N-iodosuccinimide (NIS, 3.86 g, 17.1 mmol) was heated at 65° C. under nitrogen for 4 hours. The reaction mixture was concentrated under reduced pressure and the residue was purified by flash chromatography (silica gel) using ethyl acetate/hexane (1:1 v:v). The appropriate fractions were collected according to ES MS (M+H 436) and washed with Na₂SO₃ to remove the color impurities. The fractions were concentrated under reduced pressure and dried in vacuo to afford the desired product (6.15 g, 90%) as a light yellow solid. ¹H-NMR (CD₃OD, 400 MHz) δ 7.73 (d, 1H, J=7.6 Hz), 7.47 (d, 2H, J=7.2 Hz), 7.39 (m, 4H), 7.08 (m, 3H), 6.39 (d, 1H, J=8.0 Hz), 5.29 (s, 2H), 5.19 (s, 2H); ES-HRMS m/z 436.0210 (M+H calculated for C₁₉H₁₆NO₂FI requires 436.0196).

Step 2. Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-[(trimethylsilyl)ethynyl]pyridin-2(1H)-one Degassed a solution of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one (2.01 g, 4.62 mmol) in anhydrous acetonitrile (25 mL) under argon atmosphere. Triethylamine (1.11 g, 11 mmol) was added and quickly degassed. The reaction mixture was chilled in an ice bath for 15 minutes before adding bistriphenylphosphine-palladium chloride (0.34 g, 0.48 mmol) and cuprous iodide (0.2 g). The reaction was stirred at room temperature for 30 minutes before heating at 60° C. under an atmosphere of argon for 2 hours. The reaction mixture was filtered through a bed of celite and the filtrate was concentrated under reduced pressure. The dark brown residue was diluted with CH₂Cl₂ (100 mL) and washed with water. The organic extracts were combined, dried over anhydrous Na₂SO₄, and concentrated under reduced pressure. The dark brown residue was purified by flash chromatography using 30% ethyl acetate in hexane. The appropriate fractions were combined and concentrated under reduced pressure to afford the desired product (1.34 g, 72%) as a light yellow solid. ¹H-NMR (CD₃OD, 400 MHz) δ 7.74 (d, 1H, J=7.6 Hz), 7.47 (d, 2H, J=7.6 Hz), 7.35 (m, 4H), 7.09 (m, 3H), 6.46 (d, 1H, J=7.6 Hz), 5.26 (s, 2H), 5.13 (s, 2H), 0.18 (s, 9H); ES-HRMS m/z 406.1638 (M+H calculated for C₂₄H₂₅NO₂FSi requires 406.1610).

Step 3. Preparation of 4-(benzyloxy)-3-ethynyl-1-(3-fluorobenzyl)pyridin-2(1H)-one To a solution of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-[(trimethylsilyl)ethynyl]pyridin-2(1H)-one (1.31 g, 3.2 mmol) in anhydrous acetonitrile (25 mL) at 0° C. was added tetrabutylammoniun fluoride (0.611 g, 1.93 mmol). The reaction was stirred at 0° C. for 15 minutes then for 1 hour at room temperature. The reaction was concentrated under reduced pressure and the residue was diluted with ethyl acetate and washed with water. The organic extracts were combined, dried over anhydrous Na₂SO₄ and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel) using ethyl acetate in hexane (1:1 v/v). The appropriate fractions were combined and concentrated under reduced pressure to afford the desired product (0.779 g, 72%) as a gold solid. ¹H-NMR (CD₃OD, 400 MHz) δ 7.73 (d, 1H, J=7.6 Hz), 7.43 (d, 2H, J=7.2 Hz), 7.35 (m, 4H), 7.09 (m, 3H), 6.45 (d, 1H, J=7.6 Hz), 5.27 (s, 2H), 5.13 (s, 2H), 3.78 (s, 1H); ES-HRMS m/z 334.1243 (M+H calculated for C₂₁H₁₇NO₂F requires 334.1234).

Example 415

Preparation of 4-(benzylamino)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one

Step 1. Preparation of 1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one In a Fischer-Porter bottle, added a solution of 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one (4.5 g, 14.56 mmol) in absolute ethanol (20 mL). Flushed the solution with nitrogen then added palladium catalyst (1.05 g, 10% Pd/C). Sealed bottle and evacuated system. The system was purged with hydrogen gas (2×15 psi) to check for leaks. The reaction was charged with hydrogen (35 psi) and stirred at room temperature for 45 minutes. The system was evacuated and flushed with nitrogen. The reaction was filtered and the catalyst was carefully washed with fresh ethanol. The filtrate was concentrated under reduced pressure. ¹H-NMR (CD₃OD, 400 MHz) δ 7.54 (d, 1H, J=7.6 Hz), 7.32 (m, 1H), 7.06 (d, 1H, J=7.6 Hz), 6.99 (m, 2H), 6.05 (dd, 1H, J=2.4 Hz, 2.8 Hz), 5.83 (d, 1H, J=2.4 Hz), 5.09 (s, 2H); ES-HRMS m/z 220.0774 (M+H calculated for C₁₂H₁₁NO₂F requires 220.0787).

Step 2. Preparation of 4-(benzylamino)-1-(3-fluorobenzyl)pyridin-2(1H)-one A mixture of 1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one (1.005 g, 4.5 mmol) in benzylamine (15 mL) was heated at reflux (185° C.) under nitrogen atmosphere for 24 hours. The reaction was monitored by ES-MS (MH+ 309). The solvent was removed by vacuum distillation to give a yellow residue. ¹H-NMR (CD₃OD, 400 MHz) δ 7.31 (m, 7H), 7.03 (m, 3H), 5.98 (d, 1H, J=7.2 Hz), 5.45 (s, 1H), 5.00 (s, 2H), 4.30 (s, 2H); ES-HRMS m/z 309.1403 (M+H calculated for C₁₉H₁₈N₂OF requires 309.1375).

Step 3. Preparation of 4-(benzylamino)-3-bromo-1-(3-fluorobenzyl)pyridin-2(1H)-one. To a solution of 4-(benzylamino)-1-(3-fluorobenzyl)pyridin-2(1H)-one (0.50 g, 1.62 mmol) in anhydrous CH₂Cl₂ (10 mL) was added N-bromosuccinimide (NBS, 0.30 g, 1.7 mmol). The reaction was stirred at room temperature under a nitrogen atmosphere for 3 hours. The reaction mixture was purified by flash chromatography (silica gel) using ethyl acetate in hexane (1:1 v/v). The appropriate fractions were combined and concentrated. ¹H-NMR (CD₃OD, 400 MHz) δ 7.41 (d, 1H, J=7.6 Hz), 7.31 (m, 6H), 7.04 (m, 3H), 5.99 (d, 1H, J=7.6 Hz), 5.08 (s, 2H), 4.53 (s, 2H); ES-HRMS m/z 387.0508 (M+H calculated for C₁₉H₁₇N₂OBrF requires 387.0504).

Example 416

Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-methylpyridin-2(1H)-one

Step 1. Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one A mixture of 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one (4.83 g, 15.6 mmol) and N-iodosuccinintide (NIS, 3.86 g, 17.1 mmol) in anhydrous acetonitrile (55 mL) was heated at 65° C. for 4 hours under nitrogen atmosphere. The reaction mixture was concentrated under reduced pressure and the residue was purified by flash chromatography (ethyl acetate/hexane 1:1 v/v). The appropriate fractions were collected according to ES MS (M+H 436) and washed with Na₂SO₃ to remove the color impurities. The fractions were concentrated under reduced pressure and dried in vacuo to afford the desired product (6.15 g, 90%) as a light yellow solid. ¹H-NMR (CD₃OD, 400 MHz) δ 7.73 (d, 1H, J=7.6 Hz), 7.36 (m, 6H), 7.08 (m, 3H), 6.39 (d, 1H, J=8.0 Hz), 5.28 (s, 2H), 5.19 (s, 2H); ES-HRMS m/z 436.0196 (M+H calculated for C₁₉H₁₆NO₂FI requires 436.0210).

Step 2. Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-methylpyridin-2(1H)-one To a degassed solution of 4-(benzyloxy)-1-(3-fluorobenzyl)-3-iodopyridin-2(1H)-one (1.03 g, 2.36 mmol) in anhydrous DMF (15 mL) under argon atmosphere was added triethylaamine (1.11 g, 11 mmol). The reaction mixture was chilled in an ice bath for 15 minutes before adding tetramethyl tin (2.10 g, 11.75 mmol) followed by bistriphenylphosphine-palladium chloride (0.166 g, 0.24 mmol). The reaction was stirred at room temperature for 30 minutes before heating at 95° C. under an atmosphere of argon for 3 hours. The reaction mixture was filtered through a bed of celite and the filtrate was concentrated under reduced pressure. The dark brown residue was diluted with ethyl acetate (100 mL) and washed with water. The organic extracts were combined, dried over anhydrous Na₂SO₄, and concentrated under reduced pressure. The dark brown residue was purified by flash chromatography (30% ethyl acetate in hexane). The appropriate fractions were combined and concentrated under reduced pressure to afford the desired product (0.1758 g, 22%) as a light yellow solid. The product was further purified by reverse phase HPLC using a 10-90% acetonitrile/water (30 minute gradient) at a 100 ml/min flow rate, to afford a cleaner product as a light yellow solid (0.0975 g, 8%). ¹H-NMR (CD₃OD, 400 MHz) δ 7.58 (d, 1H, J=7.6 Hz)), 7.35 (m, 6H), 6.98 (m, 3H), 6.46 (d, 1H, J=7.6 Hz), 5.19 (s, 2H), 5.15 (s, 2H), 2.0 (s, 3H); ES-HRMS m/z 324.1366 (M+H calculated for C₂₀H₁₉NO₂F requires 324.1394).

Example 417

Preparation of 1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]-3-iodopyridin-2(1H)-one

Step 1. Preparation of 1-(3-fluorobenzyl)-4-hydroxy-3-iodopyridin-2(1H)-one To a mixture of 1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one (1.1 g, 5 mmol) in acetonitrile (15 mL) was added N-iodosuccinimide (1.1 g, 5.5 mmol) along with a ca. amount of dichloroacetic acid (0.1 mL). The reaction mixture stirred at room temperature for 1 hour under nitrogen. The mixture was chilled in an ice bath and filtered cold with fresh MeCl₂. The beige solid was dried to afford the desired iodinated intermediate (1.21 g, 69%). ES-LRMS m/z 346.

Step 2. Preparation of 1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]-3-iodopyridin-2(1H)-one. To a mixture of 1-(3-fluorobenzyl)-4-hydroxy-3-iodopyridin-2(1H)-one (0.5 g, 1.44 mmol) in DMF (5 mL) was added K₂CO₃ (0.199 g, 1.44 mmol) followed by the addition of 4-fluorobenzyl bromide (0.189 mL, 1.51 mmol). The reaction mixture stirred at room temperature for 30 minutes. The mixture was diluted with ethyl acetate (50 mL) and washed with water. The organic extracts were dried over anhydrous Na₂SO₄ and concentrated to dryness. ¹H-NMR (CD₃OD, 400 MHz) δ 7.75 (d, 1H, J=7.6 Hz), 7.49 (q, 2H), 7.34 (q, 1H), 7.11 (m, 5H), 6.40 (d, 1H, J=7.6 Hz), 5.26 (s, 2H), 5.19 (s, 2H); ES-HRMS m/z 454.0098 (M+H calculated for C₁₉H₁₅NO₂F₂I requires 454.0110).

Example 418

Preparation of 1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]-3-methylpyridin-2(1H)-one

To a degassed solution of 1-(3-fluorobenzyl)-4-[(4-fluorobenzyl)oxy]-3-iodopyridin-2(1H)-one (0.804 g, 1.7 mmol) in DMF (10 mL) and LiCl (0.25 g, 5.9 mmol) was added tetramethyltin (0.49 mL, 3.54 mmol) followed by bistriphenylphosphine-palladium chloride catalyst (0.124 g, 0.177 mmol). The reaction mixture was heated in an oil bath (85°-90° C.) under nitrogen for 3 hours. The solvent was concentrated and the residue was diluted with ethyl acetate and washed with water. The organic extracts were dried over anhydrous Na₂SO₄ and concentrated to dryness. The residue was purified by flash column chromatography (20% ethyl acetate in hexane). The appropriate fractions were concentrated. ¹H-NMR (CD₃OD, 400 MHz) δ 7.59 (d, 1H, J=7.6 Hz), 7.46 (m, 2H), 7.34 (m, 1H), 7.10 (m, 4H), 6.46 (d, 1H, J=7.6 Hz), 5.17 (s, 2H), 5.15 (s, 2H), 1.99 (s, 3H); ES-HRMS m/z 342.1314 (M+H calculated for C₂₀H₁₈NO₂F₂ requires 342.1300).

Example 419

Preparation of 1-benzyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

To a degassed cold solution of DMF (10 mL) and PPh₃ (resin, 0.93 g, 2.75 mmol) was added DEAD (0.44 mL, 2.75 mmol). The reaction mixture stirred at −10° C. for 20 minutes under nitrogen. A solution of 1-benzyl-3-bromo-4-hydroxy-6-methylpyridin-2(1H)-one (0.62 g, 2.1 mmol) and 2,4-difluorobenzylalcohol (0.283 mL, 2.5 mmol) in DMF (10 mL) was added to the resin suspension. The reaction mixture stirred at −10° C. for 30 minutes and then allowed to stir at room temperature for 1 hour. The resin was filtered and rinsed with fresh MeOH and the filtrate was concentrated. The residue was dissolved in ethyl acetate and purified by flash column chromatography (ethyl acetate/hexane 1:1 v/v). The appropriate fractions were concentrated. ¹H-NMR (CD₃OD, 400 MHz) δ 7.62 (m, 1H), 7.31 (m, 3H), 7.1 (d, 2H, J=7.2 Hz), 7.02 (t, 2H, J=8.6 Hz), 6.48 (s, 1H), 5.42 (s, 2H), 5.28 (s, 2H), 2.34 (s, 3H); ES-HRMS m/z 420.0399/422.0380 (M+H calculated for C₂₀H₁₇NO₂F₂Br requires 420.0405/422.0387).

Example 420

Preparation of N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-4-fluorobenzamide

Step 1. Preparation of 4-amino-1-(3-fluorobenzyl)pyridin-2(1H)-one In a Fischer-Porter bottle, added a solution of 4-(benzylamino)-1-(3-fluorobenzyl)pyridin-2(1H)-one (2.5 g, 8.11 mmol) in glacial acetic acid (20 mL). After the solution was flushed with nitrogen, catalyst was added (10% Pd/C, 2.0 g). The vessel was sealed, evacuated, and purged with hydrogen gas. The system was charged with hydrogen gas (50 psi) and the mixture stirred at room temperature for 4 hours. The system was evacuated and flushed with nitrogen. The reaction mixture was filtered through a bed of celite and washed with fresh ethanol. The filtrate was concentrated under reduced pressure and the residue was purified by flash column chromatography (hexane/ethyl acetate 3:4 v/v). The filtrate was concentrated. ¹H-NMR (CD₃OD, 400 MHz) δ 7.32 (q, 1H), 7.02 (m, 3H), 5.93 (dd, 1H, J=2.4 Hz, 2.8 Hz), 5.58 (d, 1H, J=2.4 Hz); ES-HRMS m/z 219.0966 (M+H calculated for C₁₂H₁₂N₂OF requires 219.0928).

Step 2. Preparation of 4-fluoro-N-[1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]benzamide To a solution of 4-amino-i-(3-fluorobenzyl)pyridin-2(1H)-one (0.263 g, 1.2 mmol) in acetonitrile (7 mL) was added a DMAP (ca.), triethylamine (0.25 mL, 1.8 mmol) and 4-fluorobenzoyl chloride (0.213 mL, 1.8 mmol). The reaction mixture stirred at 0° C. for 25 minutes and then filtered. The solid was washed with 10% citric acid and water to afford the desired compound (0.326 g, 79%) after drying. ¹H-NMR (d₆DMSO, 400 MHz) δ 7.98 (m, 2H), 7.71 (d, 1H, J=7.6 Hz), 7.35 (m, 3H), 7.08 (m, 3H), 6.98 (d, 1H, J=2.4 Hz), 6.61 (dd, 1H, J=2.4 Hz, 2.4 Hz), 5.03 (s, 2H); ESLRMS m/z 341.1.

Step 3. Preparation of N-[3-bromo-1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]-4-fluorobenzamide. To a mixture of 4-fluoro-N-[1-(3-fluorobenzyl)-2-oxo-1,2-dihydropyridin-4-yl]benzamide (0.305 g, 0.89 mmol) in acetonitrile (7 mL) was added NBS (0.159 g, 0.89 mmol). The reaction mixture stirred at room temperature for 1.5 hours. The filtrate was removed under reduced pressure and the residue was purified by flash column chromatography (ethyl acetate/hexane 1:1 v/v). The fractions were concentrated. ¹H-NMR (CD₃OD, 400 MHz) δ 8.03 (m, 2H), 7.79 (d, 1H, J=7.6 Hz), 7.47 (d, 1H, J=8.0 Hz), 7.28 (m, 3H), 7.12 (m, 3H), 5.23 (s, 2H); ES-HRMS m/z 419.0202/421.0191 (M+H calculated for C₁₉H₁₄N₂O₂F₂Br requires 419.0201/421.0183).

Example 421

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one

Step 1. Preparation of 3-chloro-1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one To a mixture of 1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.30 g, 1.26 mmol) in dichloromethane (5 mL) was added NCS (2.52 g, 1.90 mmol). The reaction mixture stirred at room temperature under nitrogen for 4.5 hours. The suspension was cooled in ice bath, filtered, and the solid was rinsed with fresh dichloromethane to afford the desired product (0.271 g, 79%) as a white solid. ¹H-NMR (CD₃OD, 400 MHz) δ 7.58 (m, 1H), 7.22 (m, 2H), 6.20 (s 1H), 2.00 (s, 3H); ES-HRMS m/z 272.0287 (M+H calculated for C₁₂H₉NO₂F₂Cl requires 272.0290).

Step 2. Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one. To a solution of 3-chloro-1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.27 g, 1.00 mmol) in DMA (5 mL) was added K₂CO₃ followed by the addition of 2,4-difluorobenzyl bromide (0.128 mL, 1 mmol). The reaction mixture stirred at room temperature for 2 hours and then was diluted in water. The reaction mixture was extracted with ethyl acetate, the organic extracts were dried over Na₂SO₄ and the filtrate was concentrated. The resulting residue was purified by flash column chromatography (ethyl acetate/hexane 3:4 v/v) to afford the desired product. ¹H-NMR (CD₃OD, 400 MHz) δ 7.60 (m, 2H), 7.25 (m, 2H), 7.04 (m, 2H), 6.71 (s, 1H), 5.36 (s, 2H), 2.11 (s, 3H); ES-HRMS m/z 398.0551 (M+H calculated for C₉H₁₃NO₂F₄Cl requires 398.0571).

Example 422

Preparation of 3-bromo-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)amino]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)amino]-6-methylpyridin-2(1H)-one A mixture of 4-hydroxy-6-methylpyrone (5.0 g, 0.04 mol) and 4-fluorobenzylamine (10.0 g. 0.08 mol) in n-butanol (25.0 mL) was heated to reflux for 24 hours under argon atmosphere. The resulting solution was concentrated to dryness under reduced pressure. The residue was triturated with ethyl acetate and filtered. It was thoroughly washed with ethyl acetate and dried to afford the title compound as a pale yellow powder (4.1 g. 30%). ¹H-NMR (CD₃OD, 400 MHz) δ 7.33 (q, 2H), 7.04 (m, SH), 5.85 (d, 1H, J=2.0 Hz), 5.44 (d, 2H, J=2.4 Hz), 5.20 (s, 1H), 4.29 (s, 2H), 2.17 (s, 3H); ES-HRMS m/z 341.1488 (M+H calculated for C₂₀H₁₉N₂OF₂ requires 341.1460).

Step 2. Preparation of 3-bromo-1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)amino]-6-methylpyridin-2(1H)-one. To a solution of 1-(4-fluorobenzyl)-4-[(4-fluorobenzyl)amino]-6-methylpyridin-2(1H)-one (0.2857 g, 0.84 mmol) in MeCl₂ was added NBS (0.156 g, 0.88 mmol). The reaction stirred at room temperature under nitrogen for 45 minutes. The reaction mixture was diluted with MeCl₂ and washed with NaHCO₃. The organic extracts were washed with water, dried over Na₂SO₄, and concentrated to afford the desired product (0.3242 g, 92%) as a yellow solid. ¹H-NMR (CD₃OD, 400 MHz) δ 7.32 (q, 2H), 7.04 (m, 6H), 5.91 (s, 1H), 5.28 (s, 2H), 4.50 (s, 2H), 2.17 (s, 3H); ES-HRMS m/z 419.0549/421.0537 (M+H calculated for C₂₀H₁₈N₂OBrF₂ requires 419.0565/421.0547).

Example 423

Preparation of 3-bromo-1—(Cyclopropylmethyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

To a mixture of 3-bromo-1—(Cyclopropylmethyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.276 g, 1.07 mmol) and K₂CO₃ (0.148 g, 1.07 mmol) in DMA (4 mL) was added 2, 4-difluorobenzyl bromide (0.14 ml, 1.07 mmol). The mixture stirred at room temperature for 1.5 hours. The reaction mixture was diluted in water and extracted with ethyl acetate. The organic extracts were dried over Na₂SO₄ and concentrated. The residue was purified by flash column chromatography (ethyl acetate/hexane 1:1 v/v). The appropriate fractions were combined, and concentrated. ¹H-NMR (CD₃OD, 400 MHz) δ 7.60 (q, 1H), 7.04 (m, 2H), 6.42 (s, 1H), 5.26 (s, 2H), 4.06 (s, 1H), 4.04 (s, 1H), 2.50 (s, 3H), 0.53 (m, 2H), 0.43 (m, 2H); ES-HRMS m/z 384.0392 (M+H calculated for C₁₇H₁₇N₂OBrF₂ requires 384.0405).

Example 424

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one

Step 1. Preparation of 3-bromo-4-hydroxy-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one Commercially available 4-hydroxy-6-methyl pyrone (10 g, 79.3 mmol) was condensed with commercially available 4-(aminomethyl) pyridine (8 mL, 79.3 mmol) in water (50 mL). The mixture was heated in an oil bath at reflux for 1 hour under nitrogen. The solvent was evaporated. MS and ¹H-NMR were consistent with the desired desbrominated structure. ¹H-NMR (CD₃OD, 400 MHz) δ 8.45 (dd, 2H, J=1.6 Hz, 1.6 Hz), 7.15 (d, 2H, J=6.0 Hz), 6.00 (d, 1H, J=2.0 Hz), 5.80 (d, 1H, J=2.4 Hz), 5.34 (s, 2H), 2.23 (s, 3H); ES-LRMS (M+H) m/z 217. To a suspension of the above compound (0.801 g, 3.7 mmol) in MeCl₂ (10 mL) was added NBS (0.725 g, 4.07 mmol). The reaction mixture stirred at room temperature for 30 minutes under nitrogen. The suspension was chilled in an ice bath and filtered. The solid was washed with fresh MeCl₂ and dried to afford a beige solid (0.9663 g, 88%) after drying. ¹H-NMR (CD₃OD, 400 MHz) δ 8.47 (d, 2H, J=5.2 Hz), 7.16 (d, 2H, J=6.0 Hz), 6.09 (s, 1H), 5.40 (s, 2H), 2.24 (s, 3H); ES-LRMS (M+H) m/z 295/297.

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one To a cold solution of 2,4-difluorobenzylalcohol (0.569 mL, 5.1 mmol) in THF (5 mL) was added PPh₃ (resin, 2.55 g, 7.65 mmol) followed by the addition of DIAD (1.48 mL, 7.65 mmol). The reaction mixture stirred at −10° C. for 15 minutes under nitrogen. A solution of 3-bromo-4-hydroxy-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one (1.0 g, 3.4 mmol), in DMF (10 mL) was added to the resin suspension. The reaction mixture stirred at 0° C. for 1.5 hours and then allowed to stir at room temperature overnight. The resin was filtered and rinsed with fresh MeOH and the filtrate was concentrated. The residue was dissolved in ethyl acetate and purified by flash column chromatography (ethyl acetate). The appropriate fractions were concentrated. ¹H-NMR (CD₃OD, 400 MHz) δ 8.47 (d, 2H, J=5.6 Hz), 7.63 (q, 1H), 7.15 (d, 1H, J=5.6 Hz), 7.05 (m, 2H), 6.55 (s, 1H), 5.45 (s, 2H), 5.31 (s, 2H), 2.35 (s, 3H); ES-HRMS m/z 421.0366/423.0355 (M+H calculated for C₁₉H₁₆N₂O₂F₂Br requires 421.0358/423.0339).

Example 428

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one

Step 1. Preparation of 3-bromo-4-hydroxy-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one Commercially available 4-hydroxy-6-methyl pyrone (15 g, 119.0 mmol) was condensed with commercially available 3-(aminomethyl) pyridine (12.10 mL, 119.0 mmol) in water (75 mL). The mixture was heated in an oil bath at reflux for 1 hour under nitrogen. The solvent was evaporated. ¹H-NMR (CD₃OD, 400 MHz) δ 8.43 (d, 1H, J=4.8 Hz), 8.38 (s, 1H), 7.60 (d, 1H, J=8.0 Hz), 7.39 (dd, 1H, J=4.8 Hz, 4.8 Hz), 5.97 (d, 1H, J=2.0 Hz), 5.79 (d, 1H, J=2.4 Hz), 5.33 (s, 2H), 2.28 (s, 3H); ES-LRMS (M+H) m/z 217. To a suspension of the above compound (5.01 g, 23.1 mmol) in MeCl₂ (50 mL) was added NBS (4.53 g, 25.4 mmol). The reaction mixture stirred at room temperature for 30 minutes under nitrogen. The suspension was chilled in an ice bath and filtered. The solid was washed with fresh MeCl₂ and dried to afford a beige solid (7.89 g, 114%) after drying. ¹H-NMR (CD₃OD, 400 MHz) δ 8.44 (d, 1H, J=4.4 Hz), 8.39 (s, 1H), 7.62 (d, 1H, J=7.6 Hz), 7.39 (dd, 1H, J=5.2 Hz, 4.4 Hz), 6.07 (s, 1H), 5.39 (s, 2H), 2.29 (s, 3H); ES-LRMS (M+H) m/z 295/297.

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one The compound was prepared essentially as described in Step 2 of example 424 using 3-bromo-4-hydroxy-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one. ¹H-NMR (CD₃OD, 400 MHz) δ 8.45 (d, 1H, J=4.4 Hz), 8.41 (s, 1H), 7.63 (m, 2H), 7.41 (dd, 1H, J=5.2 Hz, 4.8 Hz), 7.02 (m, 2H), 6.52 (s, 1H), 5.44 (s, 2H), 5.29 (s, 2H), 2.40 (s, 3H); ES-HRMS m/z 421.0355/423.0358 (M+H calculated for C₁₉H₁₆N₂O₂F₂Br requires 421.0358/423.0339).

Example 435A

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-2-ylmethyl)pyridin-2(1H)-one

Step 1. Preparation of 3-bromo-4-hydroxy-6-methyl-1-(pyridin-2-ylmethyl)pyridin-2(1H)-one Commercially available 4-hydroxy-6-methyl pyrone (5 g, 39.6 mmol) was condensed with commercially available 2-(aminomethyl) pyridine (4.03 mL, 39.6 mmol) in water (25 mL). The mixture was heated in an oil bath at reflux for 1.5 hour under nitrogen. The solvent was evaporated. MS and ¹H-NMR were consistent with the desired desbromonated structure. ¹H-NMR (CD₃OD, 400 MHz) δ 8.47 (d, 1H, J=4.8 Hz), 7.75 (ddd, 1H, J=2.0 Hz, 1.6 Hz, 1.6 Hz), 7.28 (dd, 1H, J=4.8 Hz, 4.8 Hz), 7.11 (d, 1H, J=7.6 Hz), 5.98 (d, 1H, J=2.4 Hz), 5.77 (d, 1H, J=2.4 Hz), 5.35 (s, 2H), 2.28 (s, 3H); ES-LRMS (M+H) m/z 217. To a suspension of the above compound (3.0 g, 13.8 mmol) in MeCl₂ (30 mL) was added NBS (2.71 g, 15.18 mmol). The reaction mixture stirred at room temperature for 2.5 hours under nitrogen. The suspension was chilled in an ice bath and filtered. The solid was washed with fresh MeCl₂ and dried to afford a beige solid (3.18 g, 77%) after drying. ¹H-NMR (CD₃OD, 400 MHz) δ 8.46 (d, 1H, J=4.8 Hz), 7.76 (ddd, 1H, J=2.0 Hz, 1.6 Hz, 1.6 Hz), 7.29 (dd, 1H, J=5.2 Hz, 5.2 Hz), 7.17 (d, 1H, J=8.0 Hz), 6.07 (s, 1H), 5.40 (s, 2H), 2.30 (s, 3H); ES-LRMS (M+H) m/z 295/297.

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-2-ylmethyl)pyridin-2(1H)-one The compound was prepared essentially as described in Step 2 of example 424 using 3-bromo-4-hydroxy-6-methyl-1-(pyridin-2-ylmethyl)pyridin-2(1H)-one ¹H-NMR (CD₃OD, 400 MHz) δ 8.45 (d, 1H, J=4.4 Hz), 7.76 (ddd, 1H, J=2.0 Hz, 2.0 Hz, 1.6 Hz), 7.62 (q, 1H), 7.29 (dd, 1H, J=5.2 Hz, 5.6 Hz), 7.21 (d, 1H, J=8.0 Hz), 7.04 (m, 2H), 6.51 (s, 1H), 5.45 (s, 2H), 5.29 (s, 2H), 2.42 (s, 3H); ES-HRMS m/z 421.0354/423.0332 (M+H calculated for C₁₉H₁₆N₂O₂F₂Br requires 421.0358/423.0339).

Examples 425-427 and 429-437

Preparation of Compounds Corresponding in Structure to the Following Formula

The following compounds were prepared essentially according to the procedures set forth above for Example 424, using the products of Step 1 of Examples 424, 428, or 435.

Ex.										M + H m/z	ES-HRMS
No.	R1	R2	R3	R4	R5	X	Y	Z	MF	required	m/z
425	H	H	F	H	H	N	CH	CH	C19H16N2O2FBr	403.0452/	403.0444/
										405.0434	405.0414
426	F	H	F	H	F	N	CH	CH	C19H14N2O2F3Br	439.0264/	439.0270/
										441.0245	441.0274
427	F	H	H	H	F	N	CH	CH	C19H15N2O2F2Br	421.0358/	421.0378/
										423.0339	423.0368
429	H	H	F	H	H	CH	N	CH	C19H16N2O2FBr	403.0487/	403.0487/
										405.0438	405.0438
430	F	H	F	H	F	CH	N	CH	C19H14N2O2F3Br	439.0264/	439.0267/
										441.0245	441.0241
431	F	H	H	H	H	CH	N	CH	C19H16N2O2FBr	403.0452/	403.0489/
										405.0434	405.0474
432	F	H	F	F	H	CH	N	CH	C19H14N2O2F3Br	439.0264/	439.0266/
										441.0245	441.0231
433	F	H	Cl	H	H	CH	N	CH	C19H15N2O2FClBr	437.0062/	437.0068/
										439.0041	439.0041
434	Cl	H	F	H	H	CH	N	CH	C19H15N2O2FClBr	437.0062/	437.0048/
										439.0041	439.0043
435	F	H	H	H	F	CH	N	CH	C19H15N2O2F2Br	421.0358/	421.0371/
										423.0339	423.0336
436	H	H	F	H	H	CH	CH	N	C19H16N2O2FBr	403.0452/	403.0454/
										405.0434	405.0379
437	F	H	F	H	F	CH	CH	N	C19H14N2O2F3Br	439.0264/	439.0266/
										441.0245	441.0242
438	F	H	F	F	H	CH	CH	N	C19H14N2O2F3Br	439.0264/	439.0264/
										441.0245	441.0241

NMR characterization of compounds of Examples 425-427, 429-435, 436-437

Ex. No. NMR Data
425     1H-NMR (CD3OD, 400MHz) δ 8.47(d, 2H, J=5.6Hz), 7.50(q, 2H), 7.14(m, 4H), 6.49(s,
        1H), 5.44(s, 2H), 5.27(s, 2H), 2.32(s, 3H
426     1H-NMR (CD3OD, 400MHz) δ 8.48(dd, 2H, J=1.6Hz), 7.15(d, 2H, J=6.0Hz), 6.98(t, 2H,
        J=1.2Hz), 6.60(s, 1H), 5.45(s, 2H), 5.29(s, 2H), 2.36(s, 3H)
427     1H NMR (CD3OD, 400MHz) δ 8.47(d, 2H, J=1.6Hz), 7.45(m, 1H), 7.16(d, 2H, J=5.6Hz),
        7.06(t, 2H, J=8.4Hz), 6.62(s, 1H), 5.46(s, 2H), 5.34(s, 2H), and 2.37(s, 3H)
429     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=4.4Hz), 8.40(s, 1H), 7.62(d, 1H, J=8.0Hz),
        7.49(q, 2H), 7.41(dd, 1H, J=4.8Hz, 4.8Hz), 7.14(t, 2H, J=8.8Hz), 6.46(s, 1H), 5.43(s,
        2H), 5.26(s, 2H), 2.38(s, 3H)
430     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=3.6Hz), 8.42(d, 1H, J=1.2Hz), 7.60(d, 1H,
        J=8.4Hz), 7.41(dd, 1H, J=5.2Hz, 4.8Hz), 6.97(m, 2H), 6.57(s, 1H), 5.45(s, 2H), 5.27(s,
        2H), 2.42(s, 3H)
431     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=4.4Hz), 8.41(d, 1H, J=1.6Hz), 7.58(m, 2H),
        7.41(m, 2H), 7.22(m, 2H), 6.51(s, 1H), 5.44(s, 2H), 5.34(s, 2H), 2.39(s, 3H)
432     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=4.0Hz), 8.41(d, 1H, J=1.6Hz), 7.63(d, 1H,
        J=7.6Hz), 7.53(m, 1H), 7.41(dd, 1H, J=5.6Hz, 5.2Hz), 7.26(m, 1H), 6.51(s, 1H), 5.45(s,
        2H), 5.29(s, 2H), 2.40(s, 3H)
433     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=4.0Hz), 8.41(d, 1H, J=1.6Hz), 7.60(m, 2H),
        7.39(dd, 1H, J=5.2Hz), 7.28(s, 1H), 7.26(s, 1H), 6.50(s, 1H), 5.44(s, 2H), 5.31(s, 2H),
        2.40(s, 3H)
434     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=4.0Hz), 8.41(d, 1H, J=1.6Hz), 7.68(m, 2H),
        7.39(dd, 1H, J=4.8Hz, 4.8Hz), 7.31(dd, 1H, J=2.4Hz, 2.8Hz), 7.16(ddd, 1H, J=2.8Hz,
        2.8Hz, 2.8Hz), 6.50(s, 1H), 5.45(s, 2H), 5.32(s, 2H), 2.41(s, 3H)
435     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=4.0Hz), 8.42(s, 1H), 7.60(d, 1H, J=8.0Hz),
        7.47(m, 1H), 7.40(dd, 1H, J=5.2Hz, 4.8Hz), 7.07(m, 2H), 6.59(s, 1H), 5.45(s, 2H), 5.32(s,
        2H), 2.41(s, 3H)
436     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=4.8Hz), 7.76(ddd, 1H, J=2.0Hz, 1.6Hz, 1.6Hz),
        7.51(q, 2H), 7.30(dd, 1H, J=5.2Hz), 7.19(d, 1H, J=7.6Hz), 7.14(t, 2H, J=8.8Hz),
        6.46(s, 1H), 5.44(s, 2H), 5.26(s, 2H), 2.40(s, 3H)
437     1H-NMR (CD3OD, 400MHz) δ 8.46(d, 1H, J=4.8Hz), 7.76(ddd, 1H, J=2.0Hz, 1.6Hz, 1.6Hz),
        7.29(dd, 1H, J=4.8Hz, 5.2Hz), 7.21(d, 1H, J=7.6Hz), 6.69(dd, 2H, J=8.0Hz, 7.6Hz), 6.5
        7(s, 1H), 5.46(s, 2H), 5.28(s, 2H), 2.43(s, 3H)
438     1H-NMR (CD3OD, 400MHz) δ 8.45(d, 1H, J=4.4Hz), 7.76(ddd, 1H, J=2.0Hz, 1.6Hz, 1.6Hz),
        7.55(m, 1H), 7.26(m, 3H), 6.50(s, 1H), 5.46(s, 2H), 5.29(s, 2H), 2.42(s, 3H)

Example 439

Preparation of 3-bromo-4-[2-(4-fluorophenyl)ethyl]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one

Step 1. Preparation of 3-bromo-6-methyl-2-oxo-1-(pyridin-3-ylmethyl)-1,2-dihydropyridin-4-yl trifluoromethanesulfonate To a chilled suspension (−30° C.) of 3-bromo-4-hydroxy-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one (0.481 g, 1.63 mmol) in dichloromethane (6 mL) was added triethylamine (0.28 mL, 2.04 mmol), followed by the addition of a solution of trifluoromethanesulfonic anhydride (0.4 mL, 2.44 mmol) in dichloromethane (3 mL). The reaction mixture stirred at −30° C. under nitrogen for 1 hour. The reaction mixture was diluted with dichloromethane and washed with cold NaHCO₃/water. The organic extracts were dried over Na₂SO₄ and the filtrate was concentrated under reduced pressure to afford the desired compound as a yellow semisolid (0.6675 g, 95%) after drying. ES-LRMS (M+H) m/z 427.1/429.1.

Step 2. Preparation of 3-bromo-4-[(4-fluorophenyl)ethynyl]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one To a degassed solution of 3-bromo-6-methyl-2-oxo-1-(pyridin-3-ylmethyl)-1,2-dihydropyridin-4-yl trifluoromethanesulfonate (0.6675 g, 1.56 mmol) in DMF (9 mL), DIEA (0.35 mL, 2.03 mmol), 4-fluorophenylacetylene (0.235 mL, 1.95 mmol) and PdCl₂(PPh₃)₂ (0.11 g) were added. The reaction mixture stirred at room temperature under nitrogen for 1 hour and then heated in an oil bath (65° C.) under nitrogen overnight. The solvents were distilled in vacuo and the residue was purified by flash column chromatography (5% methanol in ethyl acetate). The extracts were concentrated to afford the desired compound (0.432 g, 69%) after drying. ¹H-NMR (CD₃OD, 400 MHz) δ 8.45 (s, 2H), 7.96 (s, 1H), 7.64 (m, 3H), 7.41 (dd, 1H, J=4.8 Hz, 4.8 Hz), 7.18 (t, 2H, J=8.8 Hz), 6.46 (s, 1H), 5.45 (s, 2H), 2.37 (s, 3H); ES-HRMS m/z 397.0361/399.0310 (M+H calculated for C₂₀H₁₅N₂OFBr requires 397.0346/399.0328).

Step 3. Preparation of 3-bromo-4-[2-(4-fluorophenyl)ethyl]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one A suspension of 3-bromo-4-[(4-fluorophenyl)ethynyl]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one (0.430 g, 1.01 mmol) in Ethyl acetate (5 mL) and EtOH (5 mL), containing PtO₂ (0.015 g) was stirred in an atmosphere of hydrogen (15 psi) in a Fischer-Porter bottle for 2 hours. The reaction mixture was filtered and the filtrate was concentrated to reduce volume. The material was purified by flash column chromatography (ethyl acetate). The appropriate fractions were combined and concentrated under reduced pressure to afford the desired product (0.0943 g, 22%) as a sticky semisolid after drying. ¹H-NMR (CD₃OD, 400 MHz) δ 8.46 (d, 2H, J=26.4 Hz), 7.60 (d, 1H, J=8.0 Hz), 7.41 (dd, 1H, J=4.8 Hz, 4.8 Hz), 7.21 (m, 2H), 6.97 (t, 2H, J=8.8 Hz), 6.24 (s, 1H), 5.43 (s, 2H), 2.93 (m, 4H), 2.31 (s, 3H); ES-HRMS m/z 401.0645/403.0603 (M+H calculated for C₂₀H₁₉N₂OFBr requires 401.0659/403.0641).

Example 440

Preparation of 3-bromo-4-[2-(4-fluorophenyl)ethyl]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described for Example 439, steps 1-3 (0.374 g, 25%). MS and ¹H-NMR for step 1 were consistent with the desired structure. ¹H-NMR (CD₃OD, 400 MHz) δ 8.80 (d, 2H, J=6.8 Hz), 7.89 (d, 2H, J=6.8 Hz), 6.61 (s, 1H), 5.66 (s, 2H), 2.45 (s, 3H); ES-HRMS m/z 427.9645/429.9625 (M+H calculated for C₁₃H₁₁N₂O₄SF₃Br requires 427.9599/429.9578). MS and ¹H-NMR for step 3 were consistent with the desired structure. ¹H-NMR (CD₃OD, 400 MHz) δ 8.48 (d, 2H, J=5.2 Hz), 7.21 (m, 2H), 7.13 (d, 2H, J=5.2 Hz), 6.98 (t, 2H, J=9.0 Hz), 6.26 (s, 1H), 5.43 (s, 2H), 2.95 (m, 4H), 2.25 (s, 3H); ES-HRMS m/z 401.0682/403.0636 (M+H calculated for C₂₀H₁₉N₂OFBr requires 401.0659/403.0641).

Example 441

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one

Step 1. Preparation of 3-chloro-4-hydroxy-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one To a suspension of 4-hydroxy-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one (1.016 g, 4.7 mmol) in MeCl₂ (10 mL) was added NCS (1.21 g, 1.78 mmol). The reaction mixture stirred at room temperature for 24 hours under nitrogen. The suspension was chilled in an ice bath and filtered. The solid was washed with fresh MeCl₂ and dried to afford a yellow solid (1.00 g, 85%) after drying. ¹H-NMR (CD₃OD, 400 MHz) 58.54 (m, 2H), 7.85 (d, 1H, J=1.6 Hz), 7.61 (m, 1H), 6.10 (s, 1H), 5.41 (s, 2H), 2.33 (s, 3H); ES-LRMS (M+H) m/z 251/253.

Step 2. Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one To a degassed cold solution of DMF (10 mL) and PPh₃ (resin, 2.2 g, 6.6 mmol) was added DEAD (1.038 mL, 6.6 mmol). The reaction mixture stirred at −10° C. for 20 minutes under nitrogen. A solution of 3-chloro-4-hydroxy-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one (1.00 g, 4.0 mmol) and 2,4-difluorobenzylalcohol (0.66 mL, 6.0 mmol) in DMF (10 mL) was added to the resin suspension. The reaction mixture stirred at −10° C. for 30 minutes and then allowed to stir at room temperature for 1 hour. The resin was filtered and rinsed with fresh MeOH and the filtrate concentrated. The residue was dissolved in ethyl acetate and purified by flash column chromatography (5% methanol in ethyl acetate). The appropriate fractions were concentrated. ¹H-NMR (CD₃OD, 400 MHz) δ 8.45 (ddd, 2H, J=1.6 Hz, 1.6 Hz, 1.6 Hz), 7.61 (m, 2H), 7.41 (dd, 1H, J=4.4 Hz, 4.8 Hz), 7.02 (m, 2H), 6.55 (s, 1H), 5.43 (s, 2H), 5.29 (s, 2H), 2.41 (s, 3H); ES-HRMS m/z 377.0882/379.0840 (M+H calculated for C₁₉H₁₆N₂O₂F₂Cl requires 377.0863/379.0840).

Example 442

Preparation of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-6-methyl-4-[(2,4,6-trifluorobenzyl)oxy]pyridin-2(1H)-one Trifluoroacetate

The title compound was prepared by a procedure similar to the one described for Example 385, step 2 (0.142 g, 9%). ¹H NMR (CD₃OD, 400 MHz) δ 7.64 (s, 1H), 7.00 (m, 2H), 6.66 (s, 1H), 5.29 (s, 2H), 5.18 (s, 2H), 2.50 (s, 3H), 2.47 (s, 3H); ES-HRMS m/z 469.0488/471.0464 (M+H calculated for C₁₉H₁₇N₄O₂F₃Br requires 469.0481/471.0463).

Example 443

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-methyl-4-(methylamino)pyrimidin-5-yl]methyl}pyridin-2(1H)-one Trifluoroacetate

To a solution of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride (0.15 g, 0.3 mmol) in DMF (3 mL) was added DBU (0.09 mL, 0.6 mmol). The solution was cooled in an ice bath and iodomethane (0.019 mL, 0.3 mmol) was added. The reaction mixture stirred at room temperature under nitrogen for 2 hours. The reaction was purified by reverse phase HPLC 10-90% CH3CN/water (30 minute gradient) at a flow rate of 100 mL/min. The appropriate fractions (m/z=465 M+H) were combined and freeze dried to afford the desired product (0.036 g, 25%) as a white powder. ¹H NMR (CD₃OD, 400 MHz) δ 7.72 (s, 1H), 7.60 (m, 1H), 7.03 (m, 2H), 6.62 (s, 1H), 5.31 (s, 2H), 5.16 (s, 2H), 3.77 (s, 3H), 2.60 (s, 3H), 2.47 (s, 3H); ES-HRMS m/z 465.0717/467.0712 (M+H calculated for C₂₀H₂₀N₄O₂F₂Br requires 465.0732/467.0714).

Example 444

Preparation of Ethyl N-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-methylpyrimidin-4-yl)glycinate Trifluoroacetate

The title compound was prepared by a procedure similar to the one described for Example 442 with the exception that the reaction mixture had to be heated at oil bath temperature 70° C. for 2 days (0.1384 g, 51%). ¹H NMR (CD₃OD, 400 MHz) δ 7.78 (s, 1H), 7.61 (m, 1H), 7.03 (m, 2H), 6.61 (s, 1H), 5.30 (s, 2H), 5.18 (s, 2H), 5.03 (s, 2H), 4.27 (q, 2H), 2.55 (s, 3H), 2.46 (s, 3H), 1.28 (t, 3H, J=7.0 Hz); ES-HRMS m/z 537.0936/539.0932 (M+H calculated for C₂₃H₂₄N₄O₄F₂Br requires 537.0943/539.0926).

Example 445

Preparation of N-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-methylpyrimidin-4-yl)-2-hydroxyacetamide Trifluoroacetate

To a chilled solution of 1-[(4-amino-2-methylpyrimidin-5-yl)methyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate (0.200 g, 0.38 mmol) in DMF (20 mL) and a catalytic amount of DMAP was added triethylamine (0.064 mL, 0.38 mmol). The reaction stirred at 20° C. and acetoxyacetyl chloride (0.082 mL, 0.76 mmol) was added. The reaction stirred cold for 15 minutes and then allowed to warm up to room temperature for 3 hours. The reaction was monitored by LR-ESMS m/z=466. The reaction was incomlete after 3 hours. Added acetoxyacetyl chloride (0.05 mL, 0.466 mmol), and triethylamine (0.2 mL, 1.43 mmol) to the reaction mixture and continued to stir overnight at room temperature. The next morning the reaction heated at 65° C. for 3 hours. The solvent was removed in vacuo and 1N LiOH (2.5 mL) was added to the residue. The reaction was heated at 60° C. for 5 hours. The reaction was diluted with acetonitrile and water (1:1) and purified by reverse phase HPLC in 10-90% CH₃CN/water (30 minute gradient) at a flow rate of 50 ml/min. The appropriate fractions were freeze dried to afford the desired product (0.020 g, 9%). ¹H NMR (CD₃OD, 400 MHz) δ 8.04 (s, 1H), 7.6 (m, 1H), 7.02 (m, 1H), 6.59 (s, 1H), 5.30 (s, 2H), 5.24 (s, 2H), 4.26 (s, 1H), 2.60 (s, 3H), 2.43 (s, 3H); ES-HRMS m/z 465.1161 (M+H calculated for C₂₁H₂₀N₄O₄F₂Cl requires 465.1136).

Example 446

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one

Step 1. Preparation of 3-chloro-4-hydroxy-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one To a solution of 4-hydroxy-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one (1.00 g, 4.3 mmol) in glacial acetic acid (10 mL) was added NCS (0.79 g, 5.94 mmol). The reaction mixture stirred at 60° C. for 6 hours. The solvent was removed under reduced pressure and the resulting residue was triturated with ethyl acetate. The desired product was filtered and dried (0.80 g, 69%). ¹H NMR (CD₃OD, 400 MHz) δ 8.47 (s, 1H), 8.42 (s, 1H), 6.08 (s, 1H), 5.36 (s, 2H), 2.50 (s, 3H), 2.43 (s, 3H); ES-HRMS m/z 266.0691 (M+H calculated for C₁₂H₁₃N₃O₂Cl requires 266.0691).

Step 2. Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one. To a solution of 3-chloro-4-hydroxy-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one (2.48 g, 9.3 mmol) in DMA (7 mL) was added K₂CO₃ (1.54 g, 11.0 mmol) followed by 2,4-difluorobenzyl bromide (1.2 mL, 9.3 mmol). The reaction mixture stirred at room temperature under nitrogen for 1.5 hours. The solvent was distilled in vacuo. The resulting residue was diluted in dichloromethane and washed with water. The organic extracts were concentrated and the resulting residue was purified by flash column chromatography (ethyl acetate). The appropriate fractions were combined, and concentrated. ¹H NMR (CD₃OD, 400 MHz) δ 8.49 (d, 1H, J=1.2 Hz), 8.40 (s, 1H), 7.59 (m, 1H), 7.04 (m, 2H), 6.54 (s, 1H), 5.41 (s, 2H), 5.28 (s, 2H), 2.54 (s, 3H), 2.40 (s, 3H); ES-HRMS m/z 392.1014 (M+H calculated for C₁₉H₁₇N₃O₂ClF₂ requires 392.0972).

Example 447

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(methylamino)methyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one Trifluoroacetate

To a suspension of 3-bromo-1-{[5—(Chloromethyl)pyrazin-2-yl]methyl}-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.25 g, 0.53 mmol) in THF was added methylamine (1 mL, 2.1 mmol). The reaction was sealed and stirred at room temperature overnight. The reaction mixture was diluted in water:acetonitrile (1:1) and purified by reverse phase HPLC 10-90% CH₃CN/water (30 minute gradient) at a flow rate of 70 ml/min. The appropriate fractions were combined and freeze dried to afford the desired product (0.22 g, 71%) as an amorphous solid. ¹H NMR (CD₃OD, 400 MHz) δ 8.73 (s, 1H), 8.55 (s, 1H), 7.6 (m, 2H), 7.02 (m, 1H), 6.54 (s, 1H), 5.47 (s, 2H), 5.29 (s, 2H), 4.37 (s, 2H), 2.78 (s, 3H), 2.56 (s, 3H). ES-HRMS m/z 465.0732/467.0709 (M+H calculated for C₂₀H₂₀N₄O₂BrF₂ requires 465.0732/467.0714).

Example 448

Preparation of Ethyl 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate

To a mixture of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.59 g, 2.07 mmol) and ethyl 5-(bromomethyl)pyrazine-2-carboxylate (0.62 g, 2.4 mmol) in THF (15 mL) was added NaH (0.06 g, 2.4 mmol). The reaction stirred at 60° C. for 3.5 hours. The solvent was removed under reduced pressure and the residue was partitioned over dichloromethane and citric acid (5%). The organic extracts were washed with water and dried over Na₂SO₄ (anhydrous). The organic extracts were concentrated and the residue was purified by flash column chromatography (100% ethyl acetate). The appropriate fractions were combined and concentrated under reduced pressure to remove solvent. ¹H NMR (CD₃OD, 400 MHz) δ 9.11 (d, 1H, J=1.6 Hz), 8.77 (s, 1H), 7.52 (m, 1H), 7.02 (m, 2H), 6.57 (s, 1H), 5.53 (s, 2H), 5.30 (s, 2H), 4.49 (q, 2H), 2.52 (s, 3H), 1.39 (t, 3H, J=7.2 Hz); ES-HRMS m/z 450.1045 (M+H calculated for C₂₁H₁₉N₃O₄ClF₂ requires 450.01027).

Example 449

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one

To a suspension of ethyl 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate (4.0 g, 8.9 mmol) in THF:t-butanol (1:1) (10 mL) was added NaBH₄ (0.46 g, 12.4 mmol). The reaction stirred at room temperature under argon overnight. The reaction mixture was quenched with acetic acid (2 mL) and the solvent was removed in vacuo. The residue was triturated with water and filtered. The solid was washed with fresh water followed by ethanol. The solid was purified by flash column chromatography (100% ethyl acetate). The appropriate fractions were combined and concentrated under reduced pressure to afford the desired compound (1.58 g, 44%) as a white solid. ¹H NMR (CD₃OD, 400 MHz) δ 8.59 (s, 1H), 8.56 (s, 1H), 7.52 (m, 1H), 7.01 (m, 2H), 6.55 (m, 1H), 5.45 (s, 2H), 5.29 (s, 2H), 4.71 (2H), 2.54 (s, 3H); ES-HRMS m/z 408.0940 (M+H calculated for C₁₉H₁₇N₃O₃ClF₂ requires 408.0921).

Example 450

Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylpyrazine-2-carboxamide

To a cold solution of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylic acid (0.175 g, 0.37 mmol) in DMF (5 mL, −10° C.) was added IBCF (0.046 mL, 0.35 mmol) followed by NMM (0.041 mL 0.37 mmol). The reaction was activated for 20 minutes at −15° C. after which dimethylamine (0.375 mL, 0.74 mmol) was added. The reaction stirred at −10° C. to room temperature for 45 minutes. The solvent was removed in vacuo and the residue was purified by reverse phase HPLC 10-90% CH₃CN/water (30 minute gradient) at a flow rate of 70 mL/min. The appropriate fractions were combined and freeze dried to afford the desired product (0.140 g, 75%) as a white solid. ¹H NMR (CD₃OD, 400 MHz) δ 8.68 (s, 1H), 8.67 (s, 1H), 7.52 (m, 1H), 7.02 (m, 2H), 6.54 (s, 1H), 5.50 (s, 2H), 5.30 (s, 2H), 3.11 (s, 3H), 3.07 (s, 3H), 2.55 (s, 3H); ES-HRMS m/z 493.0680/495.0657 (M+H calculated for C₂₁H₂₀N₄O₃BrF₂ requires 493.0680/495.0657).

Example 451

Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methylpyrazine-2-carboxamide

The title compound was prepared essentially as in Ex. 450, substituting dimethylamine with methylamine. ¹H NMR (CD₃OD, 400 MHz) δ 9.07 (s, 1H), 8.68 (s, 1H), 7.54 (m, 1H), 7.02 (m, 2H), 6.54 (s, 1H), 5.52 (s, 2H), 5.30 (s, 2H), 2.94 (s, 3H), 2.54 (s, 3H); ES-HRMS m/z 479.0542/481.0518 (M+H calculated for C₂₀H₁₈N₄O₃BrF₂ requires 479.0525, 481.0507).

Example 452

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(1-hydroxy-1-methylethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one

To a cold flask of MeMgBr (1.59 mL, 1.0 mmol) was added a suspension of ethyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate (0.5 g, 1.0 mmol) in THF (20 mL). The reaction stirred at 0° C. for 1.5 hours and then at room temperature overnight. The reaction was quenched with cold citric acid (25 mL, 5%) and extracted with ethyl acetate (2×100 mL). The organic extracts were washed with fresh water. The organic extracts were concentrated and purified by reverse phase HPLC 10-90% CH₃CN/water (30 minute gradient) at a flow rate of 70 ml/min. The appropriate fractions were combined and freeze dried to afford the desired product (29.9 mg, 6%). ¹H NMR (CD₃OD, 400 MHz) δ 8.76 (d, 1H, J=1.6 Hz), 8.54 (d, 1H, J=1.2 Hz), 7.52 (m, 1H), 7.02 (m, 2H), 6.52 (s, 1H), 5.45 (s, 2H), 5.29 (s, 2H), 2.55 (s, 3H), 1.52 (s, 6H); ES-HRMS m/z 480.0745/482.0722 (M+H calculated for C₂₁H₂₁N₃O₃BrF₂ requires 480.0729/482.0711).

Example 453

Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-methoxyethyl)pyrazine-2-carboxamide

The title compound was prepared essentially as in Ex. 450, substituting dimethylamine with 2-methoxyethylamine. ¹H NMR (CD₃OD, 400 MHz) δ 9.08 (d, 1H, J=1.2 Hz), 8.70 (d, 1H, J=1.2 Hz), 7.61 (m, 1H), 7.04 (m, 2H), 6.54 (s, 1H), 5.53 (s, 2H), 5.30 (s, 2H), 3.56 (m, 4H), 3.30 (s, 3H), 2.54 (s, 3H); ES-HRMS m/z 523.0822/525.0810 (M+H calculated for C₂₂H₂₂N₄O₄BrF₂ requires 523.0787/525.0770).

Example 454

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[5-(morpholin-4-ylcarbonyl)pyrazin-2-yl]methyl}pyridin-2(1H)-one

The title compound was prepared essentially as in Ex. 450, substituting dimethylamine with morpholine. ¹H NMR (CD₃OD, 400 MHz) δ 8.77 (d, 1H, J=1.6 Hz), 8.67 (s, 1H), 7.54 (m, 1H), 7.02 (m, 2H), 6.54 (s, 1H), 5.50 (s, 2H), 5.30 (s, 2H), 3.75 (s, 4H), 3.59 (dd, 4H, J=5.6 Hz, 5.2 Hz), 2.55 (s, 3H); ES-HRMS m/z 535.0816/537.0817 (M+H calculated for C₂₃H₂₂N₄O₄BrF₂ requires 535.0787/537.0770).

Example 450

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-({5-[(4-hydroxypiperidin-1-yl)carbonyl]pyrazin-2-yl}methyl)-6-methylpyridin-2(1H)-one

Step 1. Preparation of 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylic acid A mixture of ethyl 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylate (1.03 g, 2.3 mmol) in 1N NaOH (3.4 ml, 3.45 mmol, EtOH/water 1:1 v/v) stirred at room temperature for 2 hours. The reaction mixture was quenched with 5% citric acid and filtered. The solid was washed with water and dried to afford the desired product (1.011 g, 100%) as a white solid. ¹H NMR (CD₃OD, 400 MHz) δ 9.02 (s, 1H), 8.60 (s, 1H), 7.60 (m, 1H), 7.04 (m, 2H), 6.55 (s, 1H), 5.50 (s, 2H), 5.30 (s, 2H), 2.52 (s, 3H); ES-HRMS m/z 422.0732 (M+H calculated for C₁₉H₁₅N₃O₄ClF₂ requires 422.0714).

Step 2. Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-({5-[(4-hydroxypiperidin-1-yl)carbonyl]pyrazin-2-yl}methyl)-6-methylpyridin-2(1H)-one The title compound was prepared by a procedure similar to the one described for Example 453 (0.1396 g, 47%). ¹H NMR (CD₃OD, 400 MHz) δ 8.67 (s, 2H), 7.59 (m, 1H), 7.02 (m, 2H), 6.57 (s, 1H), 5.49 (s, 2H), 5.30 (s, 2H), 4.16 (m, 1H), 3.89 (septet, 1H), 3.72 (m, 1H), 3.38 (m, 2H), 2.56 (s, 3H), 1.93 (m, 1H), 1.83 (m, 1H), 1.45 (m, 2H); ES-HRMS m/z 505.1485 (M+H calculated for C₂₄H₂₄N₄O₄ClF₂ requires 505.1449).

Example 456

Preparation of 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(3-hydroxy-2,2-dimethylpropyl)pyrazine-2-carboxamide

The title compound was prepared by a procedure similar to the one described for Example 455 (0.215 g, 71%). ¹H NMR (CD₃OD, 400 MHz) δ 9.08 (d, 1H, J=1.2 Hz), 8.71 (d, 1H, J=1.6 Hz), 7.58 (m, 1H), 7.02 (m, 2H), 6.57 (s, 1H), 5.52 (s, 1H), 5.30 (s, 1H), 3.31 (s, 4H), 2.55 (s, 3H), 0.912 (s, 6H); ES-HRMS m/z 507.1630 (M+H calculated for C₂₄H₂₆N₄O₄ClF₂ requires 507.1605).

Example 457

Preparation of 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2,2,2-trifluoroethyl)pyrazine-2-carboxamide

The title compound was prepared by a procedure similar to the one described for Example 455 except no purification was required, only a NaHCO₃/ethyl acetate extraction was needed (0.2176 g, 73%). ¹H NMR (CD₃OD, 400 MHz) δ 9.11 (d, 1H, J=1.6 Hz), 8.73 (d, 1H, J=1.3 Hz), 7.59 (m, 1H), 7.02 (m, 2H), 6.57 (s, 1H), 5.53 (s, 2H), 5.30 (s, 2H), 4.01 (q, 2H), 2.54 (s, 3H); ES-HRMS m/z 503.0930 (M+H calculated for C₂₁H₁₇N₄O₃ClF₅ requires 503.0904).

Example 458

Preparation of 1-allyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1. Preparation of 1-allyl-4-hydroxy-6-methylpyridin-2(1H)-one. 4-hydroxy-6-methyl-2-pyrone (2 g, 16 mmol) was stirred in water (25 mL). Allylamine (1.2 ml, 16 mmol) was added to the reaction. The reaction was then heated to 100° C. at which point the reaction became homogeneous. The reaction was stirred at 100° C. for 2 h. The reaction was then allowed to cool to rt after which a white precipitate formed. The precipitate was isolated by suction filtration. After additional washing with water, 1.8 g (69%) of an off-white solid was obtained.

Step 2. 1-allyl-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. To a stirred solution of the above pyrone (4.0 g, 24 mmol) in DMF (75 ml) was added Cs₂CO₃ (7.8 g, 24 mmol) followed by addition of 2,4-diflurorbenzyl bromide (3.4 mmol, 26.4 mmol). The resulting mixture was stirred at rt for 2 h. Additional Cs₂CO₃ (1 g) and bromide (1 ml) was added and the reaction was stirred for an additional 2 h. The Cs₂CO₃ was removed by suction filtration. The DMF was removed under vacuum and the crude material was purified by flash chromatography. Elution with ethyl acetate-hexanes (2:1 to 1:1) afforded 1.5 g (21%) of the desired compound.

Step 3. 1-allyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. To a stirred suspension of the above pyridinone (1 g, 3.4 mmol) in CH₃CN (10 ml) was added n-bromosuccinimide (670 mg, 3.8 mmol). The reaction mixture was stirred, at rt, for 3 h. The product was obtained by filtration of the reaction mixture and washing of the solid with diethyl ether. ¹H-NMR (DMSO_d6/400 MHz) δ 7.62 (app q, J=8.8 hz, 1H), 7.31 (ddd, J=12.0, 9.6, 2.8 hz, 1H); 7.15 (app dtd, J=8.4, 2.4, 0.8 Hz, 1H); 6.50 (s, 1H); 5.87 (ddt, J=12.4, 10.4, 5.6 Hz, 1H), 5.30 (s, 2H), 5.10 (dd, J=10, 1.6 Hz, 1H), 4.87 (dd, J=17.6, 1.6 Hz, 1H), 4.64 (m, 2H), 2.34 (s, 3H); ¹⁹F-NMR (DMSO_d6/282.2 MHz) −109.68 (quin, J=1H), −113.66 (quar, J=1H); HRMS m/z 370.0255 (M+H calcd for C₁₆H₁₅BrF₂NO₂=370.0246).

Example 459

Preparation of 1-allyl-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1. 1-allyl-3-chloro-4-hydroxy-6-methylpyridin-2(1H)-one. To a stirred solution of 1-allyl-4-hydroxy-6-methylpyridin-2(1H)-one (500 mg, 3.0 mmol) in CH₃CN (10 ml), at rt, was added sequentially n-bromosuccinimide (440 mg, 3.3 mmol) and dichloroacetic acid (546 μ, 6.62 mmol). The resulting mixture was stirred for 2 h. The heterogeneous mixture was filtered and the solid was washed with additional CH₃CN to give 350 mg (59%) of the desired product as a tan solid. ¹H-NMR (DMSO_d6/300 MHz) δ 11.16 (s, 1H), 5.98-5.86 (m, 2H), 5.12 (dd, J=10.5, 1.5 Hz, 1H), 4.89 (dd, J=17.1, 1.5 Hz, 1H), 4.63-4.61 (m, 2H), 2.29 (s, 3H). ES-HRMS m/z 200.050 (M+H calcd for C₉H₁₁ClNO₂=200.0470).

Step 2. 1-allyl-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. The title compound was prepared by the procedure outline in the synthesis of Example 458, step 3. ¹H-NMR (DMSO_d6/300 MHz) δ 7.67 (app q, J=8.4 hz, 1H), 7.36 (app dt, J=10.2, 2.7 hz, 1H); 7.15 (m, 1H); 6.58 (s, 1H); 5.93 (ddt, J=15.3, 9.6, 4.8 Hz, 1H), 5.30 (s, 2H) 5.15 (dd, J=10.2, 1.2 Hz, 1H), 4.92 (dd, J=17.4, 1.2 Hz, 1H), 4.69-4.67 (m, 2H), 2.41 (s, 3H). ES-HRMS m/z 326.0760 (M+H calcd for C₁₆H₁₅ClF₂NO₂=326.0790).

Example 460

Preparation of Methyl (2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]but-2-enoate

To a stirred suspension of NaH (277 mg, 11 mmol) in anhydrous THF (30 ml), which was cooled to 0° C., was slowly added 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (3.3 g, 10 mmol). The resulting slurry was stirred for 15 min, after which methyl 4-bromocrotonate (1.4 ml, 12 mmol) was added to the reaction. The ice bath was removed and the reaction was heated to reflux for 16 h. The reaction was quenched by the addition of 1N NH₄Cl. The layers were separated and the aqueous layer was extracted with CH₂Cl₂ (5×). The organics were combined, dried, and concentrated in vacuo. The crude yellowish material was then triturated with Et₂O to give, after filtration and drying, 1.8 g (43%) of a white solid. ¹H-NMR (DMSO_d6/300 MHz) δ 7.65 (app q, J=8.7 hz, 1H), 7.36 (app dt, J=12.0, 3.0 hz, 1H); 7.17 (dt, J=8.4, 1.8 Hz, 1H); 6.94 (dt, J=15.9, 4.5 Hz, 1H); 6.57 (s, 1H), 5.52 (d, J=15.9 Hz, 1H), 5.29 (s, 2H), 4.84 (m, 2H), 3.63 (s, 3H), 2.33 (s, 3H). ES-HRMS m/z 428.0301 (M+H calcd for C₁₈H₁₇BrF₂NO₄=428.0310).

Example 461

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-prop-2-ynylpyridin-2(1H)-one

Step 1. 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-prop-2-ynylpyridin-2(1H)-one. The title compound was prepared by alkylation of 4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (2.5 g, 10 mmol) with propargyl bromide (1.3 ml, 1.0 mmol) as described above to give 1.3 g (44%) of the desired product. ¹H-NMR (DMSO_d6/300 MHz) δ 7.60 (app q, J=8.4 hz, 1H), 7.35-7.27 (m, 1H); 7.16-7.10 (m, 1H); 5.94 (d, J=2.1 Hz, 1H), 5.88 (d, J=3.0 Hz, 1H), 5.03 (s, 2H), 4.76 (d, J=2.4, Hz, 2H), 3.31 (s, 3H), 3.24 (t, J=2.4 Hz, 1H), 2.39 (s, 3H); ES-HRMS m/z 290.0994 (M+H calcd for C₁₆H₁₄F₂NO₂=290.0993).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-prop-2-ynylpyridin-2(1H)-one. Bromination of 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-prop-2-ynylpyridin-2(1H)-one (500 mg, 1.67 mmol) with NBS (300 mg, 1.67 mmol) was carried out in the manner described above to give 350 mg (57%) of the desired compound. ¹H-NMR (DMSO_d6/300 MHz) δ 7.67 (app q, J=9.0 hz, 1H), 7.36 (app dt, J=10.5, 2.4 hz, 1H); 7.23-7.16 (m, 1H); 6.60 (s, 1H), 5.29 (s, 2H), 4.90 (d, J=2.4, Hz, 1H), 3.35 (s, 3H), 3.32 (s, 1H), 2.53 (s, 3H); ES-HRMS m/z 368.0107 (M+H calcd for C₁₆H₁₃BrF₂NO₂=368.0098).

Example 462

Preparation of 4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one

Step 1. To a suspension of (4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one) (710 mg, 2 mmol) in dioxane (10 mL) was added selenium dioxide (1.1 g 10 mmol). The resulting mixture was heated to 160° C. in a 125 mL sealed tube for 1 h. The reaction was filtered through a fritted funnel. The filtrate was washed with (10:1) CH₂Cl₂-MeOH. The organics were combined and concentrated in vacuo. The crude material was purified by flash chromatography. Elution with (50:50→0:100) hexanes yielded 450 mg (63%) of the aldehyde. ¹H-NMR (DMSO_d6/400 MHz). δ 9.48 (s, 1H, CHO).

Step 2. The aldehyde (350 mg, 1 mmol) was dissolved in MeOH (4 mL) and cooled to 0° C. To this mixture was added NaBH₄ (28 mg, 1 mmol) in one portion. After 30 min, additional NaBH₄ (20 mg) was added to the reaction. The MeOH was then removed under vacuum. The residue was diluted with 1N NH₄Cl and then extracted with CH₂Cl₂(4×). The organics were combined, dried, and concentrated in vacuo. The yellowish crude product was then taken up in (1:1) CH₂Cl₂-Et₂O. After sitting for a period of time a white precipitate resulted. Filtration and washing with additional Et₂O yielded, after drying, 250 mg (55%) of the desired alcohol. ¹H-NMR (DMSO_d6/400 MHz). δ 8.42 (dd, J=4.4, 1.6 Hz, 1H) 8.37 (d, J=1.6 Hz, 1H), 7.61 (app q, J=8.0 Hz, 1H), 7.45 (d, J=8.0 Hz, 1H), 7.32-7.27(M, 2H), 7.12 (dt, J=8.4, 1.6 Hz, 1H), 6.07 (d, J=2.8 Hz, 1H), 5.99 (d, J=12.8 Hz, 1H), 5.63 (br s, 1H), 5.18 (s, 2H), 5.09 (s, 2H), 4.29 (s, 2H). LC/MS, t_r=1.19 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 359.1 (M+H).

Example 463

Preparation of 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one

The title compound was prepared by bromination of as described above to give a 60% yield. ¹H-NMR (DMSO_d6/300 MHz) δ 7.93 (d, J=7.8 Hz, 1H), 7.73-7.65 (m, 3H), 7.38 (dt, J=10.2, 2.4 Hz, 1H), 7.21 (app t, J=8.7 Hz, 2H), 6.74 (s, 1H), 5.38.-5.36 (m, 4H), 4.50 (s, 2H); ES-HRMS m/z 437.0311 (M+H cacld for C₁₉H₁₆BrF₂N₂O₂=437.0313).

Example 464

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-[(dimethylamino)methyl]-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one

The title compound was prepared in a similar manner to the procedure outlined below for 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-[(dimethylamino)-methyl]pyridin-2(1H)-one using the aldehyde (300 mg, 0.85 mmol) described above and 2.0 N THF solution of dimethylamine (500 μL, 1 mmol) to give 110 mg (34%) of a colorless oil. The oil was then dissolved in MeOH (1 mL) and stirred with fumaric acid (25 mg) for 1 h. The resulting precipitate was filtered, washed with diethyl ether, and dried to give the pure product as it's fumurate salt. ¹H-NMR (DMSO_d6/400 MHz) δ 8.43-8.41 (m, 1H), 8.35 (s, 1H), 7.67-7.61 (m, 1H), 7.44-7.40 (m, 1H), 7.35-7.29 (m, 2H), 7.17-7.12 (m, 1H), 6.62 (s, 1H), 6.60 (s, 1H), 5.41 (s, 2H), 5.32 (s, 2H), 3.13 (s, 2H), 2.12 (s, 6H). LC/MS, t_r=1.55 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 464 (M+H).

Example 465

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one

Step 1. 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde. In a 300 ml high-pressure glass reaction vessel 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde (16.3 g, 45 mmol) was dissolved in 1,4-dioxane (90 mL). The reaction vessel was sealed and immersed in a preheated oil bath at 170° C. The reaction was heated at 170° C. (165-170° C.) for 1.5 hours and then cooled to room temperature. The reaction was worked up by filtering the reaction mixture through a plug of celite and silica gel. The plug was then washed with 500 ml of methanol-CH₂Cl₂ mixture (1:5). The filtrate was evaporated to give 14.2 g of the desired crude aldehyde.

Step 2. Preparation of 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one. In a 500 ml three neck round bottom flask equipped with a stir bar of 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde (14.2 g, 37.7 mmol) was dissolved in methanol (200 mL). The reaction mixture was cooled to 0° C. and to this was added sodium borohydride (2.13 g, 56.30 mmol) in a slow portion-wise fashion. The reaction was stirred at 0° C. for 2 hour. Excess amount of sodium borohydride was added to drive the reaction to completion. After stirring for approximately 2.5 hours, the reaction was allowed to warm to room temperature and then concentrated to dryness. The residue was taken up in ethyl acetate (100 mL) and washed with dilute HCl (pH of aqueous layer was approximately 4). Organic extracts were washed with brine (1×50 ml), dried over MgSO₄, and concentrated in vacuo. The crude product was recrystallized from ethyl acetate and hexane to yield 7.56 g (44% yield-starting from step 1) of the desired alcohol.

Step 3. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one. In a 100 ml round bottom flask of 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one (2.49 g, 6.56 mmol), from step 2, was dissolved in acetonitrile (35 mL). The reaction mixture was cooled to 0° C. in ice bath for 10 min. and then charged with N-bomosuccinamide (1.17 g, 6.6 mmol). The mixture was allowed to stir, at 0° C., under nitrogen atmosphere for 2 hours. The reaction was the worked up by removing the acetonitrile under vacuum. The resulting residue was then filtered, with washing from a small amount of acetonitrile, to give a yellow solid. ¹H NMR (400 MHz, DMSO-d₆) δ 7.695-7.588 (m, 2H), 7.368-7.314 (m, 3H), 7.175 (dt, J=8.5, 2.5, Hz, 1H), 6.760 (s, 1H), 5.712 (t, J=5.674 Hz, 1H), 5.384 (s, 2H), 4.004-3.990 (m, 2H); ES-HRMS m/z 458.0013 (M+H-calcd for C₁₉H₁₃BrF₄NO₃, requires 458.0013).

Example 466

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one

The title compound was prepared by taking 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(hydroxymethyl)pyridin-2(1H)-one (1.5 g, 3.9 mmol) in acetonitrile (15 mL) and adding to that N-chlorosuccinimide (580 mg, 4.3 mmol). The reaction was stirred at rt for 3 h afterwhich a small amount of additional N-chlorosuccinimide (50 mg, 0.4 mmol) was added to the reaction. Stirring was continued for 1 h. The reaction mixture was filtered through a fritted funnel to obtain the crude material. ¹H NMR (400 MHz, DMSO-d₆) δ 7.69-7.61 (m, 2H), 7.37-7.31 (m, 3H), 7.17 (dt, J=8.8, 2.0 Hz, 1H), 6.80 (s, 1H), 5.70 (t, J=6.0 Hz, 1H), 5.38 (s, 2H), 4.01 (d, J=6.0 Hz, 2H); ES-HRMS m/z 414.0515 (M+H calcd for C₁₉H₁₃ClF₄NO₃, requires 414.0520).

Example 467

Preparation of 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde

Preparation of the title compound. In a 50 ml one neck round bottom flask 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde (0.36 g, 0.95 mmol) was dissolved in acetonitrile (5 mL). The reaction mixture was cooled to 0° C. in ice bath and charged with N-bromosuccinamide (0.17 g, 0.95 mmol). The mixture was allowed to stir at 0° C. for 2 hours under nitrogen atmosphere After 2 hours, the solvent was evaporated under vacuum. ¹H NMR (400 MHz, DMSO-d₆) δ 9.53 (s, 1H), 7.73-7.67 (m, 2H), 7.62-7.54 (m, 1H), 7.35 (dt, J=10.40, 2.56 Hz, 1H), 7.27 (t, J=8.35 Hz, 2H), 7.19 (dt, J=8.60, 2.44 Hz, 1H), 5.72 (s, 1H), 5.50 (s, 2H); ES-MS m/z 455.9836 (M+H calcd for C₁₉H₁₁BrF₄NO₃, requires 455.9859).

Example 468

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-[(dimethylamino)methyl]pyridin-2(1H)-one

In a 50 ml round bottom flask 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde (0.456 μm, 1.0 mmol) was stirred in dichloromethane (5 mL). To this mixture was added a 2M THF solution of dimethyl amine (1.25 ml, 2.5 mmol). The mixture was allowed to stir under nitrogen atmosphere and at room temperature for 2 hours. To this mixture was then added triacetoxy sodium borohydride (0.37 g, 1.75 mmol) followed by two to three drops of acetic acid. The mixture was then stirred at rt overnight. The solvents were then removed by evaporation and the residue was taken up in ethyl acetate (30 ml) and washed with aqueous sodium bicarbonate and brine. The organics were then combined, dried over MgSO₄, and concentrated in vacuo. The crude product was purified by flash column chromatography using a solvent gradient of (3:1) ethyl acetate-hexane to (0:100) ethyl acetate to give 0.14 g (30% yield) of the desired product. ¹H NMR (300 MHz, DMSO-d₆) δ 7.73-7.58 (m, 2H), 7.42-7.30 (m, 3H), 7.22 (dt, J=8.73, 2.60 Hz, 1H), 6.81 (s, 1H), 5.44 (s, 2H), 3.04 (s, 2H), 1.96 (s, 6H); ES-MS m/z 485.0 (M+H). ES-HRMS m/z 485.0457 (M+H calcd for C₂₁H₁₈BrF₄N₂O₂, requires 485.0489).

Example 469

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-(morpholin-4-ylmethyl)pyridin-2(1H)-one

The title compound was prepared by reacting 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde (0.456 g, 1 mmol) with morpholine (0.13 ml, 1.5 mmol) and triacetoxy sodium borohydride (0.42 g, 2.0 mmol) in dichloromethane (7 mL) by using a similar procedure to the one described for Example 468. The crude product was purified by flash column chromatography. Elution with (50:50→0:100) hexanes-ethyl acetate to give 0.15 g (29% yield) of the desired product. ¹H NMR (300 MHz, DMSO-d₆) δ 7.75-7.57 (m, 2H), 7.43-7.31 (m, 3H), 7.20 (dt, J=8.64, 2.48 Hz, 2H), 6.85 (s, 1H), 5.44 (s, 2H), 3.37 (app t, J=4.37 Hz, 4H), 3.13 (s, 2H), 2.08 (t, J=4.19 Hz, 4H); ES-HRMS m/z 527.0600 (M+H calcd for C₂₃H₂₀BrF₄N₂O₃ requires 527.0594).

Example 470

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-{[(2-methoxyethyl)amino]methyl}pyridin-2(1H)-one

The title compound was prepared by reacting 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde (0.319 g, 0.7 mmol) with 2-methoxy ethylamine (0.086 ml, 1.0 mmol) and triacetoxy sodium borohydride (0.42 g, 2.0 mmol) in dichloromethane (4 mL) by using a procedure, similar to the one described for Example 468. The crude product was purified by flash column chromatography. Elution with (50:50→0:100 hexanes-ethyl acetate to give 0.13 g of the desired product. ¹H NMR (400 MHz, CDCl₃) δ 7.54 (q, J=6.89 Hz, 1H), 7.41-7.33 (m, 1H), 7.19 (s, 1H), 6.99 (t, J=7.90 Hz, 2H), 6.90 (dt, J=7.90, 2.78, Hz, 1H), 6.80 (dt, J=10.60, 2.34 Hz, 1H), 6.51 (s, 1H), 5.24 (s, 2H), 3.33 (t, J=4.69 Hz, 1H), 3.30 (s, 3H), 2.57 (t, J=4.86 Hz, 2H), 1.53 (s, 2H); ES-HRMS m/z 515.0548 (M+H calcd for C₂₂H₂₀BrF₄N₂O₃, requires 515.0594).

Example 471

Preparation of 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carboxylic Acid

In a 100 ml round bottom flask, 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6 (hydroxymethyl)pyridin-2(1H)-one (1.70 g, 3.7 mmol) was dissolved in acetone (10 mL) and cooled to 0° C. in ice bath. To the reaction was added 1M acetone solution of Jones (5 ml, excess amount). Additional Jones reagent was added over time (approximately 6 hours) until the reaction was complete. The reaction was then concentrated down to dryness. The residue was then taken up in ethyl acetate (10 mL) and washed with brine. The dark yellow to brown colored crude product was purified by dissolving in 1N aqueous NaOH. The remaining organic impurities were removed by extracting with diethyl ether. The organic layers were discarded and the aqueous layer was acidified with dilute HCl (til pH app 1) to precipitate the pure acid which was then filtered and triturated with ether to obtain 1.17 g (65%) of the desired product. ¹H NMR (400 MHz, DMSO-d₆) δ 7.66 (q, J=9.41 Hz, 1H), 7.57-7.50 (m, 1H), 7.34 (dt, J=10.11, 2.78 Hz, 1H), 7.28-7.23 (m, 3H), 7.18 (dt, 8.90, 2.42 Hz, 1H), 5.47 (s, 2H). ES-HRMS f/z 471.9814 (M+H calcd for C₁₉H₁₁BrF₄NO₄, requires 471.9808).

Example 472

Preparation of Methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-methylbenzoate

Step 1: Preparation of methyl 4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-3-methylbenzoate. In a 50 ml one neck round bottom flask equipped with a stir bar, Dean Stark trap, and condenser 4-amino-2-methyl-methylbenzoate (1.19 g, 11.63 mmol) and 4-hydroxy-6-methyl-2H-pyran-2-one (1.611 g, 12.78 mmol) were mixed together and dissolved in 1,2-dichlorobenzene (5 mL). The mixture was vigorously stirred and then placed in a preheated oil bath at 165° C. The reaction was maintained at 165° C. for 1.5 hour and cooled to room temperature. The reaction was worked up by diluting with toluene (10 mL) and then stirring at room temperature for 2 hours. A light brown precipitate resulted. The crude product was isolated by filtration and then triturated with ether. ¹H NMR (400 MHz, DMSO-d₆) δ 10.64 (s, 1H), 7.93 (s, 1H), 7.85 (dd, 8.46 Hz, 1H), 7.26 (d, J=8.12 Hz, 1H), 5.91 (d, J=2.32 Hz, 1H), 5.54 (d, J=2.32 Hz, 1H), 3.84 (s, 3H), 1.99 (s, 3H), 1.73 (s, 3H). ES-HRMS m/z 272.0880 (M−H calcd for C₁₅H₁₄NO₄, requires 272.1001).

Step 2. Preparation of methyl 4-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-3-methylbenzoate Methyl 4-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-3-methylbenzoate was prepared by reacting -methyl 4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-3-methylbenzoate with N-bomosuccinamide in acetonitrile by following a procedure, similar to the one described in Example 465-step 3; ¹H NMR (400 MHz, DMSO-d₆) δ 7.95 (s, 1H), 7.87 (dd, J=7.76, 2.02 Hz, 1H), 7.31 (d, J=8.54, 1H), 6.09 (s, 1H), 3.85 (s, 3H), 1.99 (s, 3H), 1.74 (s, 1H). ES-HRMS m/z 352.0195 (M+H calcd for C₁₅H₁₄BrNO₄, requires 352.0185).

Step 3. Preparation of methyl 4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-3-methylbenzoate. The title compound was prepared by taking methyl 4-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-3-methylbenzoate (0.92 g, 2.61 mmol) and dissolving in dry DMF (5 mL). Potassium carbonate (0.432 g, 3.13 mmol) and 2,4 Difluuorobenzyl bromide (0.335 ml, 2.61 mmol) were then added. The mixture was allowed to stir at room temperature for 2 hours. The reaction was then worked up by pouring it into 100 ml of ice-water which resulted in a precipitate forming which was isolated by filtering through a fritted funnel. The crude product was washed with ether and dried in vacuum to give 0.85 g (76.20%) of pure product. ¹H NMR (400 MHz, DMSO-d₆) δ 7.98 (d, J=1.6 Hz, 1H), 7.88 (dd, J=8.04, 2.0 Hz, 1H), 7.69 (q, J=8.6 Hz, 1H), 7.36-7.30 (m, 2H), 7.17 (dt, J=8.7, 2.3 Hz, 1H), 6.71 (s, 1H), 5.32 (s, 2H), 3.86 (s, 3H), 2.00 (s, 3H), 1.86 (s, 3H). ES-HRMS m/z 478.0459 (M+H calcd for C₂₂H₁₉BrF₂NO₄ requires 478.0466).

Examples 473-476

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 473-476 are prepared by derivitazion of the compounds of Example 472.

Compound			M + H	ESHRMS
No.	R	MF	Requires	m/z
Ex. 473	—CO2H	C21H16BrF2NO4	464.0310	464.0324
Ex. 474	—CH2OH	C21H18BrF2NO3	450.0500	450.0517
Ex. 475	C(O)NH(CH2)2OCH3	C24H22BrF2N2O4	521.0888	521.0865
Ex. 476	C(O)NHCH3	C22H20BrF2N2O3	477.0626	477.0609

NMR characterization of compounds of Examples 473-476

Ex. No. NMR Data
473     1H-NMR (400MHz, DMSO-d6) δ 13.11(s, 1H), 7.95(d, J=1.70Hz, 1H), 7.86(dd, J=7.88,
        1.91Hz, 1H), 7.67(dq, J=8.47, 1.89Hz, 1H), 7.36-7.30(m, 2H), 7.17(dt, J=8.54, 2.48Hz,
        1H), 6.71(s, 1H), 5.32(s, 2H), 1.99(s, 3H), 1.87(s, 3H)
474     1H NMR (400MHz, DMSO-d6) δ 7.67(q, J=8.5Hz, 1H), 7.34(dd, J=10.04, 2.77Hz, 1H),
        7.32(s, 1H), 7.24(dd, J=8.39, 1.47Hz, 1H), 7.17(dt, J=8.84, 2.6Hz, 1H), 7.08(d, J=7.94Hz,
        1H), 6.66(s, 1H), 5.30(s, 2H), 5.25(t, J=6.01Hz, 1H), 4.5(d, J=6.68Hz, 2H), 1.91(s,
        3H), 1.86(s, 3H)
475     1H NMR (400MHz, DMSO-d6) δ 8.58(app t, J=5.4Hz, 1H), 7.84(s, 1H), 7.76(dd, J=8.06,
        1.63Hz, 1H), 7.68(dq, J=8.77, 2.04Hz, 1H), 7.33(dt, J=9.76, 2.03Hz, 1H), 7.27(d, J=8.34Hz,
        1H), 7.17(ddt, J=8.51, 2.63, 0.91Hz, 1H), 6.70(s, 1H), 5.31(s, 2H), 4.50(t, J = 5.6 Hz ,
        1H), 3.47-3.36(m, 4H), 3.24(s, 3H), 1.97(s, 3H), 1.87(s, 3H)
476     1H NMR (400MHz, DMSO-d6) δ 8.50-8.49(m, 1H), 7.82(s, 1H), 7.74(dd, J=8.22, 1.79Hz,
        1H), 7.69(q, J=6.75Hz, 1H), 7.33(dt, J=9.88, 2.57Hz, 1H), 7.26(d, J=8.52Hz, 1H), 7.17(dt,
        J=8.93, 2.16Hz, 1H), 6.69(s, 1H), 5.31(s, 2H), 2.77(d, J=4.58Hz, 3H), 1.97(s, 3H), 1.86(s,
        3H)

Example 477

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-4-vinylphenyl)pyridin-2(1H)-one

Step 1. Preparation of -1-(4-bromo-2-methylphenyl)-4-hydroxy-6-methylpyridin-2(1H)-one The title compound was prepared in a similar manner to the procedure outlined above for 4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-3-methylbenzoate. ¹H NMR (400 MHz, DMSO-d₆) δ 10.61 (s, 1H), 7.59 (d, J=2.84 Hz, 1H), 7.45 (dd, J=8.39, 2.44 Hz, 1H), 7.06 (d, J=7.44, 1H), 5.89 (d, J=2.73 Hz, 1H), 5.53(d, J=2.30, 1H), 1.91 (s, 3H), 1.75 (s, 3H). ES-HRMS m/z 294.0127 (M+H calcd for C₁₃H₁₃BrNO₃, requires 294.0130).

Step 2. Preparation of -1-(4-bromo-2-methylphenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one 1-(4-bromo-2-methylphenyl)-4-hydroxy-6-methylpyridin-2 (1H)-one (7.35 g, 25.0 mmol) was dissolved in DMF (15 mL) and stirred with potassium carbonate (4.14 g, 30.0 mmol) and 2,4 difluorobenzyl bromide (3.21 ml (25.0 mmol) at room temperature for 2 hours. The reaction was worked up by pouring in to 300 ml ice water under continuous stirring. A white precipitate was obtained which was isolated by filtering and further purified by triturating with ether to give 3.06 g (29%) of the desired product. ¹H NMR (400 MHz, DMSO-d₆) δ 7.65-7.59 (m, 2H), 7.49 (dd, J=8.45, 2.22 Hz, 1H), 7.31 (dt, J=9.79, 2.22 Hz, 1H), 7.16-7.08 (m, 2H), 6.05 (d, J=2.58 Hz, 1H), 5.93 (d, J=2.66 Hz, 1H), 5.08 (s, 2H), 1.93 (s, 3H), 1.77 (s, 3H). ES-HRMS m/z 420.0390 (M+H calcd for C₂₀H₁₇BrF₂NO₂, requires 420.0411).

Step 3. Preparation of 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-4-vinylphenyl)pyridin-2(1H)-one. In a 50 ml round bottom flask previously evacuated and filled with nitrogen, 1-(4-bromo-2-methylphenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2 (1H)-one (0.420 g, 1.0 mmol) was dissolved in dry THF (10 mL). To this mixture was added Pd (PPh₃)₄ (0.173 g, 0.15 mmol). The reaction flask was sealed with a rubber septum, evacuated and filled with nitrogen. Under a nitrogen atmosphere, tributyl(vinyl)tin (0.35 ml, 1.2 mmol) was added to the sealed reaction mixture and stirred overnight at 50° C. The reaction was worked up by quenching with water and extraction of the product with ethyl acetate. The crude product was purified by column chromatography. Elution with ethyl acetate-hexanes (50:50→0:100) hexanse gave 0.32 g (69%) of the desired product.

Step 4. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-4-vinylphenyl)pyridin-2(1H)-one. The title compound was prepared by reacting 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-4-vinylphenyl)pyridin-2(1H)-one (0.64 g, 1.74 mmol) with N-bromosuccinamide (0.325 g, 1.83 mmol) in acetonitrile (9 mL) at 0° C. using a similar procedure as described in step 3 of Example 465, to give 0.423 g (54.5% after recrystallization) of the desired product. ¹H NMR (400 MHz, DMSO-d₆) δ 7.67 (app q, J=7.59 Hz, 1H), 7.48 (s, 1H), 7.42 (dd, J=8.21, 1.98 Hz, 1H), 7.33 (dt, J=10.00, 2.27 Hz, 1H), 7.17 (dt, J=8.51, 2.44 Hz, 1H), 7.13 (d, J=7.88 Hz, 1H) 6.74 (dd, J=11.29, 6.34 Hz, 1H), 6.67 (s, 1H), 5.88 (d, J=17.85, 1H), 5.32-5.30 (m, 2H), 1.92 (s, 3H), 1.88 (s, 3H). ES-HRMS m/z 446.0579 (M+H calcd for C₂₂H₁₉BrF₂NO₂, requires 446.0568).

Example 478

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-4-vinylphenyl)pyridin-2(1H)-one (0.126 g, 0.28 mmol) was dissolved in a mixture of acetone (3 mL) and water (1 mL). To this was added 4-methylmorpholine N-oxide (0.032 g, 0.28 mmol) and catalytic amount (approximately 5 mg) of osmium tetroxide was added, and stirred under nitrogen atmosphere. After approximately 2 hours, the reaction was worked up by evaporation of the acetone. The product was extracted into ethyl acetate and concentrated to give a dark colored solid which was further purified by column chromatography to give 0.049 g (37% yield) of charcoal colored solid. ¹H NMR (400 MHz, DMSO-d₆) δ 7.67 (q, J=8.24 Hz, 1H), 7.37-7.23 (m, 3H), 7.17 (dt, J=8.62, 2.62 Hz, 1H), 7.07 (dd, J=9.36, 2.24 Hz, 1H), 6.65 (s, 1H), 5.30 (s, 2H), 4.74 (t, J=6.16 Hz, 1H), 4.57-4.50 (m, 1H), 3.45 (app t, J=6.12 Hz, 2H), 3.41-3.37 (m, 1H), 1.91 (s, 3H), 1.85 (s, 3H). ES-HRMS m/z 480.0625 (M+H calcd for C₂₂H₂₁BrF₂NO₄, requires 480.0623).

Example 479

Preparation of Methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-chlorobenzoate

Step 1. Preparation of methyl 4-chloro-3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate. A condensation reaction with methyl 3-amino-4-chlorobenzoate (14.5 g, 78.2 mmol) and 4-hydroxy-6-methyl pyranone under reaction condition similar to the one described in Example 465-step 3 gave 12.32 (53.8%) of desired product.

Step 2. Preparation of methyl-4-chloro-3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate. In a 250 ml round bottom flask, methyl 4-chloro-3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate (5.28 g, 18.0 mmol) from step 1 was reacted with 2,4-difluoro-benzylbromide (3.72 g, 18.0 mmol) in DMF using similar procedure as in Example 472 step 3. After aqueous work up and chromatographic purification, 2.3 g (30%) pure product was obtained.

Step 3. Preparation of methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-chlorobenzoate. Methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-chlorobenzoate was prepared by reacting methyl-4-chloro-3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (2.3 g, 5.47 mmol) with N-bromosuccinamide (0.97 g, 5.47 mmol) in acetonitrile (10 mL) at 0° C., using a similar procedure as described in step 3 of Example 465, to give 1.80 g (66.2%) of the desired product. ¹H NMR (400 MHz, DMSO-d₆) δ 8.06-8.03 (m, 2H), 7.86 (d, J=9.70 Hz, 1H), 7.68 (q, J=7.62, 1H), 7.34 (dt, J=10.07, 2.46 Hz, 1H), 7.17 (dt, J=8.72, 2.90 Hz, 1H), 6.73 (s, 1H), 5.33 (s, 2H), 3.85 (s, 3H), 1.91 (s, 3H). ES-MS m/z 495.9757 (M−H calcd for C₂₁H₁₄BrClF₂NO₄, requires 495.9795).

Example 480

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-chlorobenzoic Acid

In a 50 ml round bottom flask, methyl-4-chloro-3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (0.450 g, 0.90 mmol) was stirred in THF (5 mL). To this mixture was added NaOH (0.120 g, 3.0 mmol) as a solution in water (1.5 mL). The reaction mixture was stirred at room temperature overnight. The THF was evaporated and the residue was acidified with dilute HCl. A white precipitate was obtained. The product was filtered, washed with water and dried in vacuum to give 0.375 g (86% yield) of the desired product. ¹H NMR (400 MHz, DMSO-d₆) δ 7.89 (dd, J=7.78, 1.73 Hz, 1H), 7.71-7.65 (m, 2H), 7.53 (d, J=9.08 Hz, 1H), 7.33 (dt, J=9.95, 2.59 Hz, 1H), 7.17 (dt, J=8.22, 2.59 Hz, 1H), 6.68 (s, 1H), 5.32(s, 2H), 1.89 (s, 3H). ES-MS m/z 481.9585 (M−H calcd for C₂₀H₁₂BrClF₂NO₄, requires 481.9601).

Example 481

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

Step 1. Preparation of 4-hydroxy-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methyl pyridin-2(1H)-one. 4-Hydroxy-6-methyl-2-pyrone (23.0 g, 182.2 mmol) and 3-Amino-4-methylbenzyl alcohol (25.0 g, 182.2 mmol) were taken up in 25 ml of 1,2-dichlorobenzene. The solution was heated to 165° C. in a 250 ml round bottom flask equipped with a J-Kem temperature controller probe, and a heating mantle. In a separate 250 ml round bottom flask 4-Hydroxy-6-methyl-2-pyrone (23.0 g, 182.2 mmol) was suspended in 25 ml of 1,2-dichlorobenzene and also heated to 165° C. The pyrone solution was poured into the flask containing the aniline and the reaction stirred at 165° C. for 20 minutes. The reaction was allowed to cool to room temperature. Reaction contents were washed with saturated NaHCO₃ (aq.). Separated the organic and aqueous layers. Aqueous layer was made acidic with dropwise addition of concentrated HCl. The product was extracted from the acidic aqueous layer with n-BuOH. N-BuOH removed in vacuo to produce a reddish brown oil. (8.5 g, 19%). Contents carried forward to next reaction with no further purification. ¹H NMR (300 MHz, CD₃OD) δ 7.35 (m, 2H), 7.08 (s, 1H), 6.08 (br s, 1H), 5.81 (br s, 1H), 4.60 (s, 2H), 2.01 (s, 3H), 1.87 (s, 3H). LC/MS, t_r=1.42 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 246.1131 (M+H). ES-HRMS m/z 246.1107 (M+H calcd for C₁₄H₁₆NO₃ requires 246.1125).

Step 2. 4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methyl-pyridin-2(1H)-one. 4-hydroxy-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methyl pyridin-2(1H)-one from Step 1) (8.0 g, 32.6 mmol) was stirred briskly at room temperature with 2,4-difluorobenzyl bromide (4.2 ml, 32.6 mmol) and K₂CO₃ (4.5 g, 32.6 mmol) in 50 ml of dimethylformamide. After stirring for 8 hours, H₂O (100 ml) was added to reaction mixture. The product was extracted with ethyl acetate. Ethyl acetate layer was separated and dried over Na₂SO₄. Ethyl acetate was removed in vacuo. A yellow oil was obtained. The oil was passed through a plug of silica gel first eluting with 500 ml of ethyl acetate/hexane (1:1). This eluent was set aside. Next, ethyl acetate (100%) was passed through the plug until desired product was completely flushed from silica (3 liters). Solvent was removed in vacuo. Light yellow oil obtained (7.5 g, 62%). ¹H NMR (300 MHz, CD₃OD) δ 7.60 (app q, J=6.44 Hz, 1H), 7.42 (d, J=0.81 Hz, 2H), 7.15 (s, 1H), 7.06 (m, 2H), 6.21 (dd, J=1.61, 1.00 Hz, 1H), 6.12 (d, J=2.62 Hz, 1H), 5.16 (s, 2H), 4.65 (s, 2H), 2.07 (s, 3H), 1.93 (s, 3H); LC/MS, t_r=2.38 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 372 (M+H).

Step 3. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one. 4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methyl-pyridin-2(1H)-one (from Step 2) (4.0 g, 10.8 mmol) was stirred at room temperature with N-bromosuccinimide (2.1 g, 11.9 mmol) in 100 ml of CH₂Cl₂ for 2.0 hours. The reaction was evaporated on a rotary evaporator and the resulting solid was washed with acetonitrile and dried in vacuo to yield a white solid (3.9 g, 80%). ¹H NMR (300 MHz, CDCl₃) δ 7.67 (app q, J=6.24 Hz, 1H), 7.35 (d, J=1.01 Hz, 2H), 7.10 (s, 1H), 7.04 (m, 1H), 6.91 (ddd, J=11.08, 8.66, 2.42 Hz, 1H), 6.15 (d, J=0.63 Hz, 2H), 5.29 (s, 2H), 4.66 (s, 2H), 2.08 (s, 3H), 1.97 (s, 3H); ES-MS m/z 450 (M+H). ES-HRMS m/z 450.0467 (M+H calcd for C₂₁H₁₉BrF₂NO₃ requires 450.0511).

Example 482

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

The title compound was prepared by a procedure similar to the one described for Example 481, except that the product from Step 2, Example 481 was chlorinated instead of being brominated. The procedure is as follows: 4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methyl-pyridin-2(1H)-one (from Step 2, Example 481 above) (7.0 g, 18.8 mmol) was refluxed with N-chlorosuccinimide (2.5 g, 18.8 mmol) in 50 ml of CH₂Cl₂ overnight. The reaction was evaporated on a rotary evaporator and the resulting solid was stirred in MeOH. The precipitate was collected on a filter pad, washed with MeOH and dried in vacuo to yield a white solid (1.6 g, 21%). ¹H NMR (300 MHz, DMF-d₇) δ 7.85 (app q, J=6.44 Hz, 1H), 7.43 (d, J=0.81, 1H), 7.42-7.23 (m, 3H), 6.84 (s, 1H), 5.48 (s, 2H), 4.67 (s, 2H), 2.05 (s, 3H), 2.03 (s, 3H); ES-MS m/z 406 (M+H). ES-HRMS m/z 406.1033 (M+H calcd for C₂₁H₁₆ClF₂NO₄ requires 406.1016).

Example 483

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 3-amino-4-chloro-benzyl alcohol. 3-Nitro-4-chloro-benzyl alcohol (23.0 g, 122.6 mmol) is taken up in isopropyl alcohol (175 ml) and water (35 ml). Iron powder (<10 micron) (68.0 g, 1.2 moles) and NH₄Cl (66.0 g, 1.2 moles) are added. The suspension is stirred overhead at 70° C. in a three neck round bottom flask equipped with a heating mantle and a J-Kem temperature controller probe. After 4 hours, isopropyl alcohol was removed in vacuo. Water (100 ml) and concentrated HCl (10 ml) was added to mixture. Contents are transferred to a separtory funnel and ethyl acetate is used to extract the aqueous layer of impurities. The aqueous layer was then basified with 50% aqueous NaOH. The product was extracted from the basic aqueous layer with ethyl acetate. The ethyl acetate layer was dried over Na₂SO₄ and then removed in vacuo. The remaining residue was taken up in 50% ethyl acetate/hexane and the precipitate was collected on a filter pad. Precipitate was washed with 50% ethyl acetate/hexane to yield a flocculent brown solid (8.4 g, 44%). ¹H NMR (300 MHz, CD₃OD) δ 7.17 (d, J=8.26 Hz, 1H), 6.86 (d, J=2.01 Hz, 1H), 6.66 (dd, J=2.01, 0.61 Hz, 1H), 4.51 (s, 2H); LC/MS, t_r=0.32 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 158 (M+H).

Step 2. 1-[2-chloro-5-(hydroxymethyl)phenyl]-4-hydroxy-6-methylpyridin-2(1H)-one. 3-amino-4-chloro-benzyl alcohol (8.0 g, 51.0 mmol) and 4-hydroxy-6-methyl-2-pyrone (6.4 g, 51.0 mmol) were taken up in 1,2-dichlorobenzene (50 ml). The mixture was plunged into a 165° C. oil bath where it stirred for 20 minutes. The reaction was cooled to room temperature and the reaction was worked up by washing with saturated NaHCO₃ (aq.) and extracting impurities with ethyl acetate. The product remained in the aqueous layer. The basic aqueous layer was made acidic with concentrated HCl. The product was extracted from the acidic aqueous layer with ethyl acetate. The ethyl acetate layer was dried over Na₂SO₄ and the solvent removed in vacuo. The product was obtained as a yellow oil in a 26% yield and was carried through to the next step with no further purification. ¹H NMR (300 MHz, CD₃OD) δ 7.62 (d, J=8.26 Hz, 2H), 7.51 (dd, J=8.46, 2.22 Hz, 1H), 7.36 (d, J=2.01 Hz, 1H), 6.13 (br s, 1H), 5.84 (d, J=2.42 Hz, 1H), 4.68 (s, 2H), 1.97 (s, 3H); LC/MS, t_r=0.25 minutes and 1.41 minutes (tautomer), (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 266 (M+H).

Step 3. 1-[2-chloro-5-(hydroxymethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one. 1-[2-chloro-5-(hydroxymethyl)phenyl]-4-hydroxy-6-methylpyridin-2(1H)-one (from step 2) (3.5 g, 13.2 mmol) was taken up in DMF (10 ml) and cooled to 0° C. 2,4-Difluorobenzyl bromide (1.7 ml, 13.2 mmol) and K₂CO₃ (1.8 g, 13.2 mmol) were added and the reaction stirred for 6 hours. The reaction was worked up by adding saturated NaHCO₃ (aq.) and extracting with ethyl acetate. The ethyl acetate extraction was washed with water, and the aqueous layer was extracted with ethyl acetate. The organic layers were combined and dried over Na₂SO₄, filtered, and the solvent removed in vacuo. The product was obtained in 83% crude yield and carried through to the next step as a brown oil. LC/MS, t_r=2.48 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 392 (M+H). ES-HRMS m/z 392.0853 (M+H calcd for C₂₀H₁₇ClF₂NO₃ requires 392.0860).

Step 4. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one. The title compound was prepared from 1-[2-chloro-5-(hydroxymethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (from step 3) (1.8 g, 4.6 mmol) and N-bromosuccinimide (0.82 g, 4.6 mmol) by dissolving them in CH₂Cl₂ (10 ml) and stirring for 2 hours at room temperature. The solvent was removed in vacuo and the residue was taken up in CH₃CN. The precipitate was collected on a filter pad and rinsed with CH₃CN to yield a white solid (370 mg, 17%). ¹H NMR (300 MHz, CDCl₃) δ 7.65 (app q, J=6.24 Hz, 1H), 7.52 (d, J=8.26 Hz, 1H), 7.40 (dd, J=8.26, 2.01 Hz 1H), 7.26 (d, J=0.81 Hz, 1H), 7.03 (m, 1H), 6.91 (ddd, J=11.08, 8.66, 2.42 Hz, 1H), 6.17 (d, J=0.81 1H), 5.29 (s, 2H), 4.63 (s, 2H), 2.02 (s, 3H); ES-MS m/z 471 (M+H). ES-HRMS m/z 471.9953 (M+H calcd for C₂₀H₁₆BrClF₂NO₃ requires 471.9944).

Example 484

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

The title compound was prepared from 1-[2-chloro-5-(hydroxymethyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (2.4 g, 6.1 mmol) and NCS (815.0 mg, 6.1 mmol) in 65° C. dichloroethane (20 ml). A catalytic amount of dichloroacetic acid (2 drops) was added. After two hours the solvent was removed in vacuo and the residue was taken up in diethyl ether. The precipitate was collected on a filter pad and then taken up in 50% ethyl acetate/hexanes to remove residual succinimide. The precipitate was collected on a filter pad and then dried in vacuo to produce a white powder (180 mg, 6.9%). ¹H NMR (300 MHz, CDCl₃) δ 7.61 (app q, J=6.44 Hz, 1H), 7.52 (d, J=8.26 Hz, 1H), 7.40 (dd, J=8.26, 2.01 Hz 1H), 7.27 (d, J=2.01 Hz, 1H), 7.00 (m, 1H), 6.91 (m, 1H), 6.20(s, 1H), 5.29 (s, 2H), 4.65 (s, 2H), 2.03 (s, 3H); ES-MS m/z 426 (M+H). ES-HRMS m/z 426.0453 (M+H calcd for C₂₀H₁₆C₁₂F₂NO₃ requires 426.0470).

Example 485

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{5-[(dimethylamino)methyl]-2-methylphenyl}-6-methylpyridin-2(1H)-one Hydrochloride

Step 1. Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzaldehyde. 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one (1.5 g, 3.33 mmol) was dissolved in 75% CH₃CN/CH₂Cl₂ (20 ml) and cooled to 0° C. Dess-Martin Periodinane (2.8 g, 6.66 mmol) was added and the reaction stirred for four hours. At this time, the reaction was quenched with 5% sodium bisulfite (aq.). The product was extracted with ethyl acetate. The combined organic extracts were then washed with saturated NaHCO₃ (aq.). The aqueous layer was extracted with ethyl acetate. The combined organic extracts were dried over Na₂SO₄, filtered, and concentrated. The resulting residue was taken up in diethyl ether and the precipitate was collected on a filter pad and washed with more diethyl ether to yield a white solid (1.35 g, 91%). ¹H NMR (300 MHz, CDCl₃) δ 10.00 (s, 1H), 7.91 (dd, J=7.65, 1.61 Hz, 1H), 7.65 (m, 2H), 7.57 (d, J=7.85 Hz, 1H), 7.03 (m, 1H), 6.95 (ddd, J=12.69, 8.86, 2.62 Hz, 1H), 6.19 (s, 1H), 5.31 (s, 2H), 2.20 (s, 3H), 1.96 (s, 3H); ES-MS m/z 448 (M+H). ES-HRMS m/z 448.0347 (M+H calcd for C₂₁H₁₇BrF₂NO₃ requires 448.0354).

Step 2: Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzaldehyde. 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzaldehyde (from step 1) (0.50 g, 1.11 mmol) was dissolved in CH₂Cl₂ (10 ml). N,N-dimethylamine (2.0 M in THF) (1.11 ml, 2.22 mmol) was added. This mixture stirred for at room temperature for 12 hours. Next, sodium tri-acetoxyborohydride (0.47 g, 2.22 mmol) was added and the reaction stirred for two more hours. The reaction was washed with 1 N NaOH (aq.) and then extracted with CH₂Cl₂. The combined organic extracts were washed with water. The aqueous layer was separated and extracted with CH₂Cl₂. The combined organic extracts were dried over Na₂SO₄, filtered and concentrated in vacuo. The resulting residue was taken up in diethyl ether. 1M HCl in diethyl ether (5 ml) was added and the precipitate was collected on a filter pad. This precipitate was hygroscopic. The hygroscopic solid was then taken up in hot ethyl acetate. Hexane was added until a precipitate crashed out. The precipitate was collected on a filter pad to yield a white solid (150 mg, 26%). ¹H NMR (400 MHz, D₂O) δ 7.42 (m, 3H), 7.17 (s, 1H), 6.86 (m, 2H), 6.53 (s, 1H), 5.20 (s, 2H), 4.18 (s, 1H), 2.72 (s, 6H), 1.85 (s, 3H), 1.82 (s, 3H); ES-MS m/z 477 (M+H). ES-HRMS m/z 477.0955 (M+H calcd for C₂₃H₂₄BrF₂N₂O₂ requires 477.0984).

Example 486

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{5-[(isopropylamino)methyl]-2-methylphenyl}-6-methylpyridin-2(1H)-one Hydrochloride

The title compound was prepared by reductive amination of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzaldehyde (from step 1) (0.50 g, 1.11 mmol) with iso-propyl amine (0.13 g, 2.22) according to the procedure described above for Example 485 (Step 2) to give the desired compound (0.49 g, 84%). ¹H NMR (400 MHz, CD₃OD) δ 7.64 (app quartet, J=6.58 Hz, 1H), 7.53 (m, 2H), 7.29(br s, 1H), 7.03 (m, 1H), 6.68 (s, 1H), 5.36 (s, 2H), 4.22 (s, 2H), 3.46 (m, 1H), 2.06 (s, 3H), 2.01 (s, 3H), 1.37 (d, J=6.58 Hz, 6H); ES-MS m/z 491 (M+H). ES-HRMS m/z 491.1107 (M+H calcd for C₂₄H₂₆BrF₂N₂O₂ requires 491.1140).

Example 487

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide

Step 1. Preparation of methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-methylbenzoate. 4-Hydroxy-6-methyl-2-pyrone (22.9 g, 181.6 mmol) and methyl-3-amino-2-methylbenzoate (25 g, 151.3 mmol) were suspended in 50 ml of 1,2-dichlorobenzene in a 250 ml, 3-necked round bottom flask equipped with a J-Kem temperature controller probe, a Dean-Stark trap, and a heating mantle. The reaction was heated to 165° C. for 15 minutes, during which, water and some 1,2-dichlorobenzene was collected in the Dean-Stark trap. The reaction was allowed to cool to about 110° C. At this point, 200 ml of toluene was added. The flask was plunged into a 0° C. ice bath while stirring. “Oiling out” occurred. Perhaps too much toluene was added so some of the solvent was removed in vacuo. The oil went back into solution and a light brown precipitate remained. The toluene mixture was allowed to stir for 72 hours at room temperature. A precipitate was collected on a filter pad. The precipitate was filtered and washed 3 times with toluene, 3 times with 50° C. water to remove excess pyrone, and dried in vacuo to give a tan solid (16.5 g, 40% yield). ¹H NMR (300 MHz, CD₃OD) δ 8.06 (dd, J=8.06, 1.61 Hz, 1H), 7.80 (d, J=1.61 Hz, 1H), 7.56 (d, J=8.06, Hz, 1H), 6.15 (dd, J=2.42, 0.81 Hz, 1H), 5.86 (d, J=2.42 1H), 3.94 (s, 3H), 2.15 (s, 3H), 1.91 (s, 3H); ES-MS m/z 274 (M+H). ES-HRMS m/z 274.1066 (M+H calcd for C₁₅H₁₆NO₄ requires 274.1074).

Step 2. Preparation of methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate. Methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-methylbenzoate (from Step 1) (16.5 g, 60.4 mmol) 2,4-difluorobenzyl bromide (7.8 ml, 60.4 mmol) were taken up in 250 ml of N,N-dimethylformamide and the mixture was cooled to 0° C. K₂CO₃ (8.3 g, 60.4 mmol) was added and reaction stirred for 12 hours during which time the reaction was allowed to warm to room temperature. LC/MS indicated the presence of starting material after 12 hours. An excess of K₂CO₃ was added at room temperature along with 0.50 ml of 2,4-difluorobenzyl bromide. The reaction stirred for an additional two hours. Saturated NaHCO₃ (aq.) was poured into reaction vessel. The solution was extracted with ethyl acetate and the organic layers were combined then washed with water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The organic layers were combined and dried over Na₂SO₄, and evaporated. The product was carried on to the next step as a crude oil (24.1 g, quantitative yield). ¹H NMR (300 MHz, CDCl₃) δ 8.06 (dd, J=7.85, 1.61 Hz, 1H), 7.82 (d, J=1.61, 1H), 7.52-7.44 (m, 2H), 7.01-6.88 (m, 2H), 6.05 (d, J=2.62 Hz, 1H), 5.97 (dd, J=2.62, 0.81 Hz, 1H), 5.08 (s, 2H), 3.93 (s, 3H), 2.20 (s, 3H), 1.89 (s, 3H); ES-MS m/z 400 (M+H). ES-HRMS m/z 400.1374 (M+H calcd for C₂₂H₂₀F₂NO₄ requires 400.1355).

Step 3. Preparation of 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid. Methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (14 g, 35.0 mmol)(from step 2) was taken up in THF (25 ml) and H₂O. 2.5 N NaOH (aq.) was added and the reaction stirred for 30 minutes at room temperature. The reaction was made acidic via the addition of concentrated HCl. The product was extracted with ethyl acetate. The ethyl acetate extraction was dried over Na₂SO₄, filtered, and the solvent removed in vacuo. Upon vacuum removal of the solvent, the product crashed out of the ethyl acetate. This precipitate was collected on a filter pad and washed with a 50 ethyl acetate/hexanes to yield a white powder (9 g, 7%). ¹H NMR (300 MHz, CDCl₃) δ 8.01 (dd, J=, 1.61 Hz, 1H), 7.84 (d, J=1.61 Hz, 1H), 7.52-7.47 (app q, J=8.26, 1H), 7.43 (d, J=8.06 Hz, 1H), 7.00-6.88 (m, 2H), 6.19 (d, J=2.62 Hz, 1H), 6.05 (dd, J=2.62, 1.81 Hz, 1H), 5.17 (s, 2H), 2.19 (s, 3H), 1.90 (s, 3H); ES-HR/MS m/z 386.12 (M+H calcd for C₂₁H₁₈F₂NO₄ requires 386.1198).

Step 4: Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid. 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (5.9 g, 15.2 mmol) (from step 3 above) was taken up in dichloromethane (25 ml). N-Bromosuccinimide was added and the reaction stirred for 14 hours. The dichloromethane was removed in vacuo and the residue was taken up in acetonitrile. The precipitate was collected on a filter pad and rinsed with acetonitrile to yield the desired product as a white, solid (5.2 g, 74%). ¹H NMR (300 MHz, CD₃OD) δ 7.87 (dd, J=7.85, 1.61, Hz, 1H), 7.82 (d, J=1.81 Hz, 1H), 7.69 (app q, J=8.06 Hz 1H), 7.57 (d, J=8.06 Hz, 1H), 7.09 (dt, J=8.66, 2.22 Hz, 1H), 6.70 (s, 1H), 5.40 (s, 2H), 2.14 (s, 3H), 2.02 (s, 3H); ES-MS m/z 464 (M+H). ES-HRMS m/z 464.0275 (M+H calcd for C₂₁H₁₇BrF₂NO₄ requires 464.0304).

Step 5. Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide. 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (from Step 4 above) (1.9 g, 4.10 mmol) was dissolved in 20 ml of CH₂Cl₂. Ethanolamine (297 μl, 4.92 mmol) was added, followed, in order, by EDCI (0.764 g, 4.92 mmol), 1-hydroxybenzotriazole (0.665 g, 4.92 mmol) and triethylamine (1.14 ml, 8.20 mmol). The reaction was stirred at room temperature overnight. The reaction was quenched with NH₄Cl and extracted 3 times with ethyl acetate. The combined organic layer was then washed with saturated NaHCO₃ (aq.) and extracted 3 times with ethyl acetate. The organic layers were combined and washed with H₂O and extracted 3 times with ethyl acetate. The organic layers were combined and dried over Na₂SO₄ and evaporated. The resulting residue was triturated with diethyl ether/hexane to obtain a solid, which was dried in vacuo to give a white solid (1.5 g, 72%). ¹H NMR (300 MHz, CDCl₃) δ 7.93 (dd, J=7.85, 1.61 Hz, 1H), 7.65 (d, J=1.61 Hz, 1H), 7.62 (app q, J=8.26 Hz, 1H), 7.40 (d, J=8.06 Hz, 1H), 7.39-7.30 (m, 1H), 7.03-6.97 (m, 1H), 6.88-6.81 (m, 1H), 6.25 (s, 1H), 5.20 (s, 2H), 3.70-3.52 (m, 1H), 3.16-3.12 (m, 2H), 2.10 (s, 3H), 1.98 (s, 3H); ES-MS m/z 507 (M+H). ES-HRMS m/z 507.0719 (M+H calcd for C₂₃H₂₂BrF₂N₂O₄ requires 507.0726).

Examples 488-491

Preparation of Compounds Corresponding in Structure to the Following Formula

The compounds of Examples 488-491 are prepared essentially according to the procedures

Compound		%		M + H	ESHRMS
No.	R	Yield	MF	Requires	m/z
Ex. 488	—NH(CH2)2OCH3	84	C24H24BrF2N2O4	528.0882	521.0868
Ex. 489	—NHCH3	79	C22H20BrF2N2O3	477.0620	477.0602
Ex. 490	—N(CH3)2	54	C23H22BrF2N2O3	491.0776	491.0753
Ex. 491	-morpholine	65	C25H24BrF2N2O4	533.0858	533.0882

Example 492

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(1-hydroxy-1-methylethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

Step 1. Preparation of methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate. Methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (as prepared above) (1.8 g, 4.51 mmol) was taken up in CH₂Cl₂ (10 ml). N-bromosuccinimide (0.80 g, 4.51 mmol) was added and the mixture stirred at room temperature for two hours. The CH₂Cl₂ is removed in vacuo and the residue is taken up in CH₃CN. The resulting precipitate is collected on a filter pad and washed with CH₃CN to yield a white solid (0.30 g, 14%, first crop). ¹H NMR (300 MHz, CDCl₃) δ 8.06 (dd, J=8.06, 1.61 Hz, 1H), 7.80 (d, J=1.61 Hz, 2H), 7.65 (app q, J=8.46 Hz, 1H), 7.48 (d, J=8.06, 1H), 7.05-6.99 (m, 1H), 6.96-6.89 (m, 1H), 6.16 (s, 1H), 5.31 (s, 2H), 3.93 (s, 3H), 2.17 (s, 3H), 1.96 (s, 3H). ES-HRMS m/z 478.0476 (M+H calcd for C₂₂H₁₉BrF₂NO₄ requires 478.0476).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(1-hydroxy-1-methylethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one. Methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (0.22 g, 0.46 mmol) was taken up in THF and cooled to 0° C. MeMgCl (3.0 M in THF) (0.73 ml, 2.2 mmol) was slowly added to the 0° C. solution. The reaction was allowed to proceed without maintaining the 0° C. bath temperature. The reaction was complete within two hours. At this time the mixture was quenched with saturated NH₄Cl (aq.) and extracted with ethyl acetate. The organic layers were combined, washed with H₂O, and extracted with ethyl acetate. The organic layers were combined and dried over Na₂SO₄, filtered, and evaporated. The residue was taken up in 50% ethyl acetate/hexanes. The precipitate was collected on a filter pad and washed with 50% ethyl acetate/hexanes to yield a white solid (0.10 g, 45%). ¹H NMR (300 MHz, CD₃OD) δ 7.70 (app q, J=8.26, Hz, 1H), 7.54 (dd, J=8.06, 2.01 Hz, 1H), 7.40 (d, J=1.81 Hz, 1H), 7.12-7.06 (m, 2H), 6.68 (s, 1H), 5.40 (s, 2H), 2.05 (s, 3H), 2.02 (s, 3H), 1.57 (s, 6H). ES-HRMS m/z 478.0785 (M+H calcd for C₂₃H₂₃BrF₂NO₃ requires 478.0824).

Example 493

Preparation of Methyl 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

The title compound was prepared by taking up methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (1.46 g, 3.66 mmol) in dichloroethane (25 ml) and adding N-chlorosuccinimide (0.49 g, 3.66 mmol), dichloroacetic acid (catalytic), and heating to 50° C. for 6 hours. At this time, the solvent was removed in vacuo and the residue taken up in diethyl ether. The precipitate was collected on a filter pad. ¹H NMR (300 MHz, CDCl₃) δ 8.07 (dd, J=7.85, 1.61 Hz, 1H), 7.80 (d, J=1.81 Hz, 2H), 7.62 (app q, J=8.46 Hz, 1H), 7.48 (d, J=7.85, 1H), 7.05-6.95 (m, 1H), 6.93-6.89 (m, 1H), 6.19 (s, 1H), 5.30 (s, 2H), 3.93 (s, 3H), 2.17 (s, 3H), 1.97 (s, 3H). ES-HRMS m/z 434.0932 (M+H calcd for C₂₂H₁₉ClF₂NO₄ requires 434.0965).

Example 494

Preparation of Methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-chlorobenzoate

Step 1. Preparation of methyl 3-chloro-4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate. 4-Hydroxy-6-methyl-2-pyrone (24.5 g, 193.9 mmol) and methyl-3-amino-2-chlorobenzoate (30 g, 161.6 mmol) were suspended in 75 ml of 1,2-dichlorobenzene in a 250 ml, 3-necked round bottom flask equipped with a J-Kem temperature controller probe, a Dean-Stark trap, and a heating mantle. The reaction was heated to 175° C. for 20 minutes, during which, water and some 1,2-dichlorobenzene was collected in the Dean-Stark trap. The reaction was allowed to cool to about 110° C. At this point, 200 ml of toluene was added. The toluene mixture was allowed to stir for 72 hours at room temperature. A precipitate was collected on a filter pad. The precipitate was filtered and washed 3 times with toluene, 3 times with 50° C. water to remove excess pyrone, and dried in vacuo to give a tan solid (13.0 g, 27% yield). ¹H NMR (300 MHz, CD₃OD) δ 8.26 (d, J=1.81 Hz, 1H), 8.14 (dd, J=8.26, 1.81 Hz, 1H), 7.54 (d, J=8.26, Hz, 1H), 6.14(dd, J=2.42, 1.0 Hz, 1H), 5.83 (d, J=2.42 1H), 4.00 (s, 3H), 1.96 (s, 3H); LC/MS, t_r=1.81 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 294 (M+H).

Step 2. Preparation of methyl 3-chloro-4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate. Methyl 3-chloro-4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate (from Step 1) (2.4 g, 8.17 mmol) was taken up in DMF (10 ml). 2,4-difluorobenzylbromide (1.05 ml, 8.17 mmol) and K₂CO₃ (1.13 g, 8.17 mmol) were added. The reaction stirred for 6 hours at room temperature. At this time, the reaction was poured into water (200 ml) and extracted with ethyl acetate. The ethyl acetate layer was dried over Na₂SO₄, filtered, and the solvent removed in vacuo to give amber oil (2.62 g, 77% crude yield). LC/MS, t_r=2.79 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 294 (M+H).

Step 3. Preparation of methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-chlorobenzoate. Methyl 3-chloro-4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (from step 2) (2.60 g, 6.21 mmol) was taken up in CH₂Cl₂ (20 ml). N-bromosuccinimide (1.11 g, 6.21 mmol) was added and the mixture stirred at room temperature for 4 hours. The CH₂Cl₂ is removed in vacuo and the residue is taken up in CH₃CN. The resulting precipitate is collected on a filter pad and washed with CH₃CN to yield a white solid (0.75 g, 24%). ¹H NMR (300 MHz, CDCl₃) δ 8.22 (d, J=1.88 Hz, 1H), 8.06 (dd, J=8.19, 1.75 Hz, 1H), 7.59 (app q, J=8.46 Hz, 1H), 7.33 (d, J=8.19, 1H), 6.96 (dt, J=8.06, 1.21 Hz, 1H), 6.89-6.84 (m, 1H), 6.13 (s, 1H), 5.26 (s, 2H), 3.95 (s, 3H), 1.95 (s, 3H). ES-HRMS m/z 497.9892 (M+H calcd for C₂₂H₁₆BrClF₂NO₄ requires 497.9914).

Example 495

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)amino]-1-(3-fluorobenzyl)pyridin-2(1H)-one

Step 1. Preparation of 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with 4-benzyloxy-2(1H)-pyridinone (20 g, 99.6 mmol) and N,N-dimethyl formamide (50 mL). K₂CO₃ (13.7 g, 99.6 mmol) and KI (1.6 g, 9.6 mmol) were added followed by 3-fluorobenzyl bromide (14.6 mL, 119.4 mmol). The reaction mixture was heated for 18 h at 80 C. The reaction mixture was concentrated in vacuo and treated with hot ethyl acetate. The solids were filtered off, the filtrate was poured into water and was extracted with ethyl acetate. The organic extract was washed with brine, dried with anhydrous Na₂SO₄, and concentrated in vacuo. The residue was dissolved in hot ethyl acetate and precipitated with hexanes to give the title compound (10 g, 33%). ¹H NMR (400 MHz, CD₃OD) δ 7.57 (d, J=8.4 Hz, 1H), 7.37 (m, 5H), 7.07 (d, J=8.4 Hz, 1H), 7.01 (app d, J=8.4 Hz, 2H), 6.17 (d, J=2.68 and 7.6 Hz, 1H), 6.04 (d, J=2.68 Hz, 1H), 5.10 (s, 2H), 5.08 (s, 2H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −114.88 (1 F) ppm. ES-HRMS m/z 310.1271 (M+H calcd for C₁₉H₁₇FNO₂ requires 310.1238).

Step 2. Preparation of 1-(3-fluorobenzyl)-4-hydroxypyridin-2(1H)-one A small Parr bottle was charged with (10 g, 32.3 mmol), ethanol (175 mL) and 10% Pd/C (0.5 g). The system was flushed twice with both nitrogen and hydrogen. The reaction mixture was hydrogenated at 30 psi until no starting material was visible by LC-MS. The reaction mixture was slurried with Celite and then was filtered through a pad of celite. The filtrate and ensuing ethanol washes were concentrated in vacuo to give a beige solid. ¹H NMR (400 MHz, CD₃OD) δ 7.53 (d, J=7.67 Hz, 1H), 7.32 (m, 1H), 7.06 (d, J=7.6 Hz, 1H), 6.98 (d, J=8.4 Hz, 2H), 6.05 (dd, J=2.58 and 7.67 Hz, 1H), 5.83 (d, J=2.0 Hz, 2H), 5.10 (s, 2H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −115.33 (1 F) ppm. ES-HRMS m/z 218.0641 (M+H calcd for C₁₂H₁₁FNO₂ requires 218.0612).

Step 3. Preparation of 4-[(2,4-difluorobenzyl)amino]-1-(3-fluorobenzyl)pyridin-2(1H)-one The product from Step 2 (0.5 g, 2.28 mmol) and 2,4-difluoro benzylamine (4 mL, 33.6 mmol) were combined in a nitrogen flushed culture tube. The tube was capped and heated at 180 C for 24 h. The excess amine was distilled in vacuo and the residue was chromatographed on silica (95:5 ethyl acetate: methanol). The final compound was isolated as a light yellow solid (0.16 g, 36%). ¹H NMR (400 MHz, CD₃OD) δ 7.33 (m, 3H), 7.03 (d, J=8 Hz, 1H), 6.96 (m, 3H), 6.95 (m, 1H), 5.97 (dd, J=3.2 and 8.0 Hz, 1H), 5.48 (d, J=2.56 Hz, 1H), 5.02 (s, 2H), 4.33 (s, 2H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −113.88 (1 F), −115.33 (1F), −116.78 (1F) ppm. ES-HRMS m/z 345.1221 (M+H calcd for C₁₉H₁₇F₃N₂O requires 345.1209).

Step 4. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)amino]-1-(3-fluorobenzyl)pyridin-2(1H)-one N-Bromo succinimide (81 mg, 0.46 mmol) was added to a solution of the product from Step 3 (0.15 g, 0.44 mmol) in methylene chloride (10 mL). After stirring at 25 C for 1 h, the reaction was complete by LC-MS. The reaction mixture was poured into saturated aqueous NaHCO₃. The aqueous mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried with anhydrous MgSO₄, and concentrated in vacuo. ¹H NMR (400 MHz, CDCl₃) δ 7.3-7.2 (m, 4H), 7.07 (app t, J=7.6 Hz, 2H), 6.97 (m, 2H), 6.80 (m, 2H), 5.78 (d, J=7.6 Hz, 1H), 5.30 (br s, 1H), 5.08 (s, 2H), 4.46 (d, J=6 Hz, 2H) ppm. ¹⁹F NMR (400 MHz, CDCl₃) δ −110.64 (1 F), −112.75 (1F), −114.79 (1F) ppm. ES-HRMS m/z 423.0275 (M+H calcd for C₁₉H₁₅BrF₃N₂O requires 423.0314).

Example 496

Preparation of 3-bromo-1-(3-fluorobenzyl)-4-{[3-(trifluoromethyl)benzyl]amino}pyridin-2(1H)-one

The title compound was prepared essentially as in Example 495. ¹H NMR (400 MHz, CDCl₃) δ 7.54 (m, 2H), 7.48 (m, 2H), 7.27 (q, J=3.1, 9.0 Hz, 1H), 6.96 (app t, J=8.8 Hz, 2H), 5.71 (d, J=7.6 Hz, 1H), 5.4 (br m, 1H), 5.08 (s, 2H), 4.52 (d, J=5.6 Hz, 2H) ppm. ¹⁹F NMR (400 MHz, CDCl₃) 6-63 (3 F), −112 (1 F) ppm. ES-HRMS m/z 455.0388 (M+H calcd for C₂₀H₁₆BrF₄N₂O requires 455.0377).

Example 497

Preparation of 3-bromo-1-(3-fluorobenzyl)-4-{[4-fluoro-2-(trifluoromethyl)benzyl]amino}pyridin-2(1H)-one

The title compound was prepared essentially as in Example 495. ¹H NMR (400 MHz, CDCl₃) δ 7.43 (m, 2H), 7.27 (m, 3H), 7.07 (m, 2H), 6.99 (m, 2H), 5.65 (d, J=10 Hz, 1H), 5.46 (br s, 1H), 5.09 (s, 2H), 4.64 (s, 2H) ppm. ¹⁹F NMR (400 MHz, CDCl₃) 6-61.31 (3 F), −112.69 (1 F), 112.97 (1F) ppm. ES-HRMS m/z 473.0246 (M+H calcd for C₂₀H₁₅BrF₅N₂O requires 473.0282).

Example 498

Preparation of -bromo-4-[(4-chloro-2-fluorobenzyl)amino]-1-(3-fluorobenzyl)pyridin-2(1H)-one

The title compound was prepared essentially as in Example 495. ¹H NMR (400 MHz, CDCl₃) δ 7.27 (m, 1H), 7.19 (app t, J=8.8 Hz, 1H), 7.10 (m, 4H), 6.95 (app t, J=8.8 Hz, 2H), 5.74 (d, J=8 Hz, 1H), 5.40 (br s, 1H), 5.08 (s, 2H), 4.47 (d J=6 Hz, 2H) ppm. ¹⁹F NMR (400 MHz, CDCl₃) δ −112.67 (1 F), −116.39 (1 F) ppm. ES-HRMS m/z 439.0047 (M+H calcd for C₁₉H₁₅ClBrF₂N₂O requires 439.0019).

Example 499

Preparation of

The title compound was prepared essentially as in Example 495. ¹H NMR (400 MHz, CDCl₃) δ 7.35-7.2 (m, 1H), 7.27 (dd, J=2.5 and 8 Hz, 1H), 7.05 (app d, J=7.2 Hz, 3H), 6.97 (m, 4H), 5.72 (d, J=7.6 Hz, 1H), 5.41 (br s, 1H), 5.08 (s, 2H), 4.46 (d, J=6.4 Hz, 2H) ppm. ¹⁹F NMR (400 MHz, CDCl₃) 6-112.5 (1 F), −113 (1 F) ppm. ES-HRMS m/z 405.0431 (M+H calcd for C₁₉H₁₆BrF₂N₂O requires 405.0409).

Example 500

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)amino]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one

Step 1. Preparation of 4-[(2,4-difluorobenzyl)amino]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one 4-[(2,4-Difluorobenzyl)amino]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one (0.3 g, 1.39 mmol) and 2,4-difluoro benzylamine (1 mL, 8.4 mmol) were combined in a nitrogen flushed culture tube. The tube was capped and heated at 180 C for 24 h. The excess amine was distilled in vacuo. ¹H NMR (400 MHz, CD₃OD) δ 8.44 (dd, J=1.7 and 4.8 Hz, 2H), 7.38 (q, J=10 and 15 Hz, 1H), 7.14 (d, J=4.8 Hz, 2H), 6.95 (m, 2H), 5.90 (dd, J=1 and 2.5 Hz, 1H), 5.47 (d, J=2, 1H), 5.28 (s, 2H), 4.33 (s, 2H), 2.27 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −113.73 (1 F), −116.66 (1 F) ppm. ES-HRMS m/z 342.1422 (M+H calcd for C₁₉H₁₈F₂N₃O requires 342.1418).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)amino]-6-methyl-1-(pyridin-4-ylmethyl)pyridin-2(1H)-one N-Bromo succinimide (77 mg, 0.43 mmol) was added to a solution of the product of Step 1(0.14 g, 0.41 mmol) in methylene chloride (10 mL). After stirring at 25 C for 1 h, the reaction was complete by LC-MS. The reaction mixture was poured into saturated aqueous NaHCO₃. The aqueous mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried with anhydrous Na₂SO₄, filtered and concentrated in vacuo. The residue was triturated with hexanes to give the title compound as a yellow solid (81 mg, 47%). ¹H NMR (400 MHz, CDCl₃) δ 8.47 (dd, J=1.6 and 4.8 Hz, 2H), 7.24 (q, J=6.4 and 13.6 Hz, 1H), 7.01 (d, J=6.4 Hz, 2H), 6.83 (m, 2H), 5.68 (s, 1H), 5.25 (s, 2H), 4.45 (d, J=6.4 Hz, 2H), 2.12 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CDCl₃) δ −110.51 (m, 1 F), −114.66 (m, 1 F) ppm. ES-HRMS m/z 420.0524 (M+H calcd for C₁₉H₁₇BrF₂N₃O requires 420.0523).

Example 501

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)amino]-6-methyl-1-(pyridin-3-ylmethyl)pyridin-2(1H)-one

The title compound was prepared essentially as in Example 500. ¹H NMR (400 MHz, CDCl₃) δ 8.45 (d, J=4.8 Hz, 2H), 7.55 (app t, J=6 Hz, 1H), 7.21 (m, 2H), 6.83 (m, 2H), 5.65 (s, 1H), 5.34 (d, J=5.2 Hz, 1H), 5.27 (s, 2H), 4.45 (s, 2H), 2.10 (d, J=4.8 Hz, 3H) ppm. ¹⁹F NMR (400 MHz, CDCl₃) δ −110.74 (1 F), −114.86 (1 F) ppm. ES-HRMS m/z 420.0533 (M+H calcd for C₁₉H₁₇BrF₂N₃O requires 420.0523).

Example 502

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)amino]-1-(2,6-difluorophenyl)-6-methylpyridin-2(I H)-one

Step 1 Preparation of 4-[(2,4-difluorobenzyl)amino]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one

1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.3 g, 1.26 mmol) and 2,4-difluoro benzylamine (1 mL, 8.4 mmol) were combined in a nitrogen flushed culture tube. The tube was capped and heated at 180 C for 24 h. The excess amine was distilled in vacuo and the residue was chromatographed on silica (1:1 hexanes: ethyl acetate). The compound was approximately 50% pure and was carried on without further purification (0.633 g). ¹H NMR (400 MHz, CD₃OD) δ 7.53 (m, 1H), 7.41 (m, 1H), 7.16 (t, J=8.8 Hz, 2H), 6.93 (m, 2H), 6.00 (s, 1H), 5.42 (s, 1H), 5.42 (s, 1H), 4.37 (s, 2H), 1.93 (s, 3H) ppm. LC/MS, t_r=4.65 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 363 (M+H).

Step 2 Preparation of 3-bromo-4-[(2,4-difluorobenzyl)amino]-1(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one

N-Bromo succinimide (168 mg, 0.945 mmol) was added to a solution of the product of Step 1(0.633 g) in methylene chloride (10 mL). After stirring at 25 C for 1 h, the reaction was 50% complete by LC-MS. Additional N-bromo succinimide (150 mg) was added and the reaction was stirred at 25 C for 12 h. The reaction mixture was poured into saturated aqueous NaHCO₃. The aqueous mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried with anhydrous Na₂SO₄, and concentrated in vacuo. The residue was purified by reverse phase chromatography (60:40 Acetonitrile: water with 0.05% trifluoroacetic acid). The title compound was isolated as the TFA salt (0.161 g, 23%). ¹H NMR (400 MHz, CD₃OD) δ 7.53 (m, 1H), 7.35 (q, J=8, 15.6 Hz, 1H), 7.16 (t, J=8 Hz, 2H), 6.96 (app q, J=8, 16.4 Hz, 2H), 6.12 (s, 1H), 4.86 (s, 2H), 1.94 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −77.33 (1 F), −113.60 (1 F), −116.63 (1F), −121.50 (1F) ppm. ES-HRMS m/z 441.0231 (M+H calcd for C₁₉H₁₄BrF₄N₂O requires 441.0220).

Example 503

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)amino]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one

1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.3 g, 1.26 mmol) and 2,4-difluoro benzylamine (1 mL, 84 mmol) were combined in an nitrogen flushed culture tube. The tube was capped and heated at 180 C for 24 h. The excess amine was distilled in vacuo and the residue was used without further purification. N-Chloro succinimide (168 mg, 1.26 mmol) was added to a solution of the residue in methylene chloride (10 mL). After stirring at 25 C for 1 h, the reaction mixture was poured into saturated aqueous NaHCO₃. The aqueous mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried with anhydrous Na₂SO₄, and concentrated in vacuo. The residue was chromatographed on silica (25:75 hexanes: ethyl acetate) to give the title compound (32 mg, 6%). ¹H NMR (400 MHz, CD₃OD) δ 7.55 (m, 1H), 7.36 (q, J=9.2 and 15.2 Hz, 1H), 7.18 (t, J=7.6 Hz, 2H), 6.98 (m, 2H), 6.15 (s, 1H), 4.62 (s, 2H), 1.96 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −113.78 (1 F), −116.72 (1 F), −121.57 (1F) ppm. ES-HRMS m/z 397.0752 (M+H calcd for C₁₉H₁₄ClF₄N₂O requires 397.0725).

Example 504

Preparation of 3-{[3-chloro-4-[(2,4-difluorobenzyl)amino]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

Step 1 Preparation of 3-phthalimidomethyl-benzonitrile

3-Phthalimidomethyl-benzonitrile was prepared as described in the literature. (Bookser, B. C.; Bruice, T. C. J. Am. Chem. Soc. 1991, 113, 4208-18.)

Step 2 Preparation of 3-(aminomethyl)benzonitrile

3-(Aminomethyl)benzonitrile was prepared as described in the literature. (Bookser, B. C.; Bruice, T. C. J. Am. Chem. Soc. 1991, 113, 4208-18.)

Step 3 Preparation of 3-[(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)methyl]benzonitrile

A nitrogen flushed pyrex reaction tube was charged with 3-(aminomethyl)benzonitrile (1 g, 7.9 mmol), 4-hydroxy-6-methyl-2-pyrone (1 g, 7.9 mmol) and water (20 mL). The tube was capped and was heated to reflux. After 1.5 h, the product precipitated from solution. The reaction mixture was cooled to room temperature, filtered and washed with water. The product was used without further purification (1.67 g, 88%). ¹H NMR (400 MHz, dmso-d₆) δ 10.53 (s, 1H), 7.61 (d, J=8 Hz, 1H), 7.52 (t, J=8 Hz, 2H), 7.38 (d, J=8 Hz, 1H), 5.79 (dd, J=1 and 2.5 Hz, 1H), 5.56 (d, J=2.7 Hz, 1H), 5.18 (s, 2H), 2.14 (s, 3H) ppm. ES-HRMS m/z 241.0968 (M+H calcd for C₁₄H₁₃N₂O₂ requires 241.0972).

Step 5 Preparation of 3-{[4-[(2,4-difluorobenzyl)amino]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

The product from Step 4 (0.5 g, 2.08 mmol) and 2,4-difluoro benzylamine (2 mL, 16.8 mmol) were combined in a nitrogen flushed culture tube. The tube was capped and heated at 180 C for 24 h. The excess amine was distilled in vacuo and the residue was triturated with ethyl acetate/hexanes to precipitate the starting materials. The residue was chromatographed on reverse phase (1:1 water: acetonitrile with 0.05% trifluoroacetic acid). The product of Step 5 was isolated as a white semi-solid (0.125 g, 15%). ¹H NMR (400 MHz, CD₃OD) δ 7.61(d, J=8 Hz, 1H), 7.49 (t, J=8 Hz, 1H), 7.41 (m, 3H), 6.94 (m, 2H), 5.89 (dd, J=0.8 and 2.7 Hz, 1H), 5.47 (d, J=2.8 Hz, 1H), 5.27 (s, 2H), 4.34 (s, 2H), 2.18 (s, 3H) ppm. LC/MS, t_r=4.87 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 366 (M+H).

Step 6 Preparation of 3-{[3-chloro-4-[(2,4-difluorobenzyl)amino]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

N-Chloro succinimide (36 mg, 0.27 mmol) was added to a solution of the product of Step 5 (0.125 g, 0.26 mmol) in methylene chloride (10 mL). After stirring at 25 C for 2 h, the reaction was complete by LC-MS. The reaction mixture was poured into saturated aqueous NaHCO₃. The aqueous mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried with anhydrous Na₂SO₄, and concentrated in vacuo. The residue was triturated with acetonitrile to give the title compound as a tan solid (20 mg, 13%). ¹H NMR (400 MHz, CD₃OD) δ 7.61 (d, J=8.4 Hz, 1H), 7.49 (m, 2H), 7.40 (d, J=8.4 Hz, 1H), 7.33 (q, J=8.4 and 14.8 Hz, 1H), 6.94 (m, 2H), 6.00 (s, 1H), 5.34 (s, 2H), 4.56 (s, 2H), 2.21 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −114.00 (1 F), −116.89 (1 F) ppm. LC/MS, t_r=5.49 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 400 (M+H).

Example 505

Preparation of 4-{[3-chloro-4-[(2,4-difluorobenzyl)amino]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzonitrile

The title compound was prepared essentially as in Example 504. ¹H NMR (400 MHz, CD₃OD) δ 7.66 (d, J=8 Hz, 2H), 7.33 (q, J=8 and 15.2 Hz, 1H), 7.25 (d, J=8 Hz, 2H), 6.94 (m, 2H), 6.01 (s, 1H), 5.36 (s, 2H), 4.55 (s, 2H), 2.19 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −77.52 (1F), −113.89 (1 F), −116.71 (1 F) ppm. LC/MS, t_r=5.49 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 400 (M+H).

Example 506

Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2-fluoro-5-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one

Step 1 Preparation of (3-amino-4-fluorophenyl)methanol

A flask equipped with overhead stirrer was charged with 4-fluoro-3-nitrobenzyl alcohol (20 g, 0.117 mol) and 200 mL of 5:1 isopropanol:water. Ammonium chloride (62 g, 1.17 mol) was added followed by iron filings (65 g, 1.17 mol). The mixture was stirred at 70 C for 1.5 H when it was shown to be complete by LC-MS. The liquid was decanted and the solids were washed with additional isopropanol: water. The isopropanol was removed and the residue was diluted with 0.5 N HCl and was extracted with ethyl acetate. The aqueous layer was brought to pH 12-14 with 2.5 N NaOH and was extracted with ethyl acetate. The organic layer was dried with anhydrous Na₂SO₄ and concentrated in vacuo. 3-Amino-4-fluorophenyl methanol was isolated as a brown solid (4.5 g, 27%) and was used without further purification. LC/MS, t_r=2.40 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 142 (M+H). ES-HRMS m/z 142.0692 (M+H calcd for C₇H₈FNO requires 142.0663).

Step 2 Preparation of 1-[2-fluoro-5-(hydroxymethyl)phenyl]-4-hydroxy-6-methylpyridin-2(1H)-one

A 100 mL round bottomed flask equipped with stirbar, Dean-Stark trap and reflux condensor was charged with (3-amino-4-fluorophenyl)methanol (4.5 g, 31.9 mmol), 4-hydroxy-6-methyl-2-pyrone (4 g, 31.9 mmol) and o-dichlorobenzene (5 mL). The system was immersed in a 170 C oil bath for 10 minutes. The solvent was removed in vacuo and the residue was chromatographed on reverse phase (75:25 water:acetonitrile with 0.05% TFA). The product contained some starting materials after purification and was used without further purification (1.27 g, 15%). ¹H NMR (400 MHz, dmso-d₆) δ 7.39 (m, 1H), 7.20 (dd, J=2.2 and 7.6 Hz, 1H), 6.74 (dd, J=2.7 and 9.6 Hz, 1H), 5.93 (dd, J=1.2 and 2.2 Hz, 1H), 5.22 (dd, J=0.4 and 2.2 Hz, 1H), 2.12 (s, 3H) ppm. ES-HRMS m/z 250.0862 (M+H calcd for C₁₃H₁₃FNO₃ requires 250.0874).

Step 3 Preparation of 4-[(2,4-difluorobenzyl)oxy]-1-[2-fluoro-5-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one

A 100 mL roundbottomed flask (nitrogen purged) was charged with 1-[2-fluoro-5-(hydroxymethyl)phenyl]-4-hydroxy-6-methylpyridin-2(1H)-one (1.2 g, 4.82 mmol) and N,N-dimethyl formamide (10 mL). Potassium carbonate (0.6 g, 4.4 mmol) and 2,4-difluorobenzyl bromide (0.56 mL, 4.4 mmol) was added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with saturated aqueous NaHCO₃ and extracted with ethyl acetate. The organic layer was concentrated in vacuo and the residue was chromatographed on silica (9:1 methylene chloride: ethanol). The impure oil (0.3 g, 17%) was carried on without further purification. ¹H NMR (400 MHz, CD₃OD) δ 7.54 (m, 2H), 7.30 (m, 2H), 7.02 (m, 2H), 6.17 (dd, J=1 and 2.8 Hz, 1H), 6.03 (d, J=2.8 Hz, 1H), 5.14 (s, 2H), 4.62 (s, 2H), 2.14 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.35 (1F), −115.97 (1 F), −127.31 (1 F) ppm. LC/MS, t_r=5.05 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 375 (M+H).

Step 4 Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2-fluoro-5-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one

N-Bromo succinimide (50 mg, 0.3 mmol) was added to a solution of the product of Step 3 (0.12 g, 0.32 mmol) in N,N-dimethyl formamide (4 mL). After stirring at 25 C for 2 h, trifluoroacetic acid (50 μL) was added. After 1 h, additional N-Bromo succinimide (30 mg) was added. After 1 h, the reaction was complete by LC-MS. The reaction mixture was poured into brine and was extracted with ethyl acetate. The organic layer was washed with brine, dried with anhydrous Na₂SO₄, and concentrated in vacuo. The residue was chromatographed on reverse phase (95:5 methylene chloride: ethanol). The title compound was isolated as the TFA salt (38 mg, 26%). ¹H NMR (400 MHz, CD₃OD) δ 7.64 (q, J=7.6 and 14.8 Hz, 1H), 7.51 (m, 1H), 7.31 (app t, J=8.4 Hz, 1H), 7.04 (t, J=8.4 Hz, 2H), 6.63 (s, 1H), 5.34 (s, 2H), 4.62 (s, 2H), 2.06 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.48 (1F), −115.92 (1 F), −127.23 (1 F) ppm. ES-HRMS m/z 454.0228 (M+H calcd for C₂₀H₁₆BrF₃NO₃ requires 454.0260).

Example 507

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid

Step 1 Preparation of Methyl 4-fluoro-3-nitrobenzoate

A 1 L 3-necked round bottomed flask equipped with a nitrogen inlet, stirbar, addition funnel and thermocouple was charged with 4-fluoro-3-nitrobenzoic acid (50 g, 0.27 mol) and methanol (300 mL). The system was cooled to 0 C and acetyl choride (27 mL, 0.37 mol) was added dropwise. The system was warmed to room temperature, the addition funnel was replaced with a reflux condensor, and was heated to reflux for 1.5 h. The reaction mixture was cooled to room temperature, quenched with saturated aqueous NaHCO₃, and extracted with ethyl acetate. The organic extract was washed with brine, dried with Na₂SO₄ and concentrated in vacuo to give methyl 4-fluoro-3-nitrobenzoate as an orange solid (40.6 g, 75%). ¹H NMR (400 MHz, CD₃OD) δ 8.67 ((dd, J=2.2 and 6.8 Hz, 1H), 8.34 (dddd, J=2.2, 4.4, 6.4 and 8.8 Hz, 1H), 7.55 (dd, J=8.8 and 10.8 Hz, 1H), 3.94 (s, 3H) ppm. ES-HRMS m/z 200.02446 (M+H calcd for C₈H₇FNO₄ requires 200.0354).

Step 2 Preparation of Methyl 3-amino-4-fluorobenzoate

A Parr bottle was charged with the product of Step 1(40 g, 0.2 mol), ethanol (400 mL) and 10% Pd/C (1 g g). The system was flushed twice with nitrogen and hydrogen. The reaction mixture was hydrogenated at 40 psi until no starting material was visible by LC-MS. The reaction mixture was slurried with Celite and then was filtered through a pad of celite. The filtrate and ensuing ethanol washes were concentrated in vacuo to give methyl 3-amino-4-fluorobenzoate as an orange solid (30.6 g, 91%). ¹H NMR (400 MHz, CD₃OD) δ 7.54 (d, J=8.7 Hz, 1H), 7.35 (m, 1H), 7.06 (t, J=8.7 Hz, 1H), 3.09 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −131.02 (1F) ppm. ES-HRMS m/z 199.0281 (M+H calcd for C₈H₇FNO₄ requires 199.02).

Step 3 Preparation of Methyl 4-fluoro-3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate

A 250 mL round bottomed flask equipped with stirbar, Dean-Stark trap and reflux condensor was charged with the product of Step 3 (30 g, 0.18 mol), 4-hydroxy-6-methyl-2-pyrone (22.6 g, 0.18 mol), and o-dichlorobenzene (90 mL). The system was immersed in a 170 C oil bath for 30 minutes and was then cooled to room temperature. The reaction mixture was washed with aqueous Na₂CO₃ (38 g, 0.36 mol, 300 mL water). The aqueous layer was washed with ethyl acetate and then was acidified to pH 1-2 with concentrated HCl. This was extracted with ethyl acetate, which was then dried with MgSO₄ and concentrated in vacuo. The viscous orange oil was used without further purification (14.4 g, 28%). ¹H NMR (400 MHz, CD₃OD) δ 8.18 (dddd, J=2.3, 5.2, 7.2 and 8.8 Hz, 1H), 7.97 (dd, J=2 and 7.2 Hz, 1H), 7.44 (t, J=8.8 Hz, 1H), 6.09 (d, J=1.8 Hz, 1H), 5.78 (d, J=2.4 Hz, 1H), 3.9 (s, 3H), 2.14 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −117.29 (1F) ppm. ES-HRMS m/z 278.0796 (M+H calcd for C₁₄H₁₃FNO₄ requires 278.0823).

Step 4 Preparation of Methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoate

A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the product of Step 3 (14.4 g, 51.9 mmol) and N,N-dimethyl formamide (40 mL). 1,8-diazabicyclo[5.4.0]undec-7-ene (10.9 mL, 72.8 mmol) was added followed by 2,4-difluorobenzyl bromide (9.3 mL, 72.8 mmol). The reaction mixture was stirred at 65 C for 18 h, was poured into saturated aqueous NaHCO₃ and was extracted with ethyl acetate. The organic layer was washed with brine, dried with Na₂SO₄ and concentrated in vacuo to give the title product, as an orange oil (21.5 g), which was carried on to the next reaction without further purification. ¹H NMR (400 MHz, CD₃OD) δ 8.20 (dddd, J=2.2, 4.8, 7.2 and 8.8 Hz, 1H), 8.00 (dd, J=2.2 and 7.2 Hz, 1H), 7.56 (td, J=2.4, 6.4 and 9.2 Hz, 1H), 7.46 (t, J=9.2 Hz, 1H), 7.02 (m, 2H), 6.18 (dd, J=0.8 and 2.6 Hz, 1H), 6.04 (d, J=2.7 Hz, 1H), 5.14 (s, 2H), 3.90 (s, 3H), 1.98 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.34 (1F), −116.00 (1 F), −117.35 (1 F) ppm. ES-HRMS m/z 404.1104 (M+H calcd for C₂₁H₁₇F₃NO₄ requires 404.1104).

Step 5 Preparation of Methyl 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoate

A 250 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the product of Step 4 (21 g, 52 mmol) and N-methyl-2-pyrrolidine (100 mL). N-Chloro succinimide (8.3 g, 62 mmol) was added and the reaction mixture was stirred at 65 C for 2 h. The mixture was then cooled to room temperature, poured into saturated aqueous NaHCO₃ and extracted with ethyl acetate. The organic layer was washed with brine, dried with Na₂SO₄, and concentrated in vacuo. The residue was triturated with diethyl ether and filtered to give the title compound, as a white powder (5.9 g, 25%). ¹H NMR (400 MHz, CD₃OD) δ 8.22 (dddd, J=2, 4.8, 6.8 and 8.8 Hz, 1H), 8.03 (dd, J=2 and 7.2 Hz, 1H), 7.62 (q, J=8.4 and 14.8 Hz, 1H), 7.48 (t, J=14 Hz, 1H), 7.04 (m, 2H), 6.69 (s, 1H), 5.36 (s, 2H), 3.91 (s, 3H), 2.08 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.38 (1F), −115.97 (1 F), −117.43 (1 F) ppm. ES-HRMS m/z 438.0723 (M+H calcd for C₂₁H₁₆ClF₃NO₄ requires 438.0714).

Step 6 Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic Acid

A 100 mL round bottomed flask was charged with the product of Step 5 (2.5 g, 5.72 mmol), tetrahydrofuran (40 mL), methanol (10 mL), and water (10 mL). To this slurry was added 2.5 N NaOH (4.6 mL, 11.4 mmol). The reaction mixture became clear after 5 minutes and the reaction was complete in 35 minutes by LC-MS. The organics were removed on the rotary evaporator and the remaining solution was acidified to pH 3 with 6N HCl. The desired compound was precipitated by the addition of diethyl ether and subsequent filtration. The title compound was isolated as a white powder (2.5 g, 98%). ¹H NMR (400 MHz, dmso-d₆) δ 8.10 (dddd, J=2.1, 4.8, 7.2 and 8.4 Hz, 1H), 8.00 (dd, J=2.1 and 7.6 Hz, 1H), 7.66 (q, J=9.2 and 15.6 Hz, 1H), 7.57 (t, J=8.8 Hz, 1H), 7.34 (td, J=2.4 and 10.4 Hz, 1H), 7.17 (tdd, J=1, 2.7 and 8.4 Hz, 1H), 6.76 (s, 1H), 5.33 (s, 2H), 1.98 (s, 3H) ppm. ¹⁹F NMR (400 MHz, dmso-d₆) δ −109.32 (1F), −113.64 (1 F), −117.22 (1 F) ppm. ES-HRMS m/z 424.0575 (M+H calcd for C₂₀H₁₄ClF₃NO₄ requires 424.0558).

Example 508

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluoro-N-methylbenzamide

To a reaction vessel (borosilicate culture tube) was added 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid (0.300 g, 0.708 mmol) and 1-hydroxybenzotriazole (0.048 g, 0.45 mmol). N,N-Dimethylformamide (3 mL) was added to the reaction vessel followed by approximately 1.2 g of the polymer bound carbodiimide resin (1.38 mmol/g). Additional N,N-dimethylformamide (2 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. N-Methyl amine (1 mL, 2 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with tetrahydrofuran (20 mL) and treated with approximately 2.17 g of polyamine resin (2.63 mmol/g) and approximately 2.8 g of methylisocyanate functionalized polystyrene (1.5 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 3 hours. The reaction vessel was then opened and the solution phase product was separated from the insoluble quenched byproducts by filtration and collection into a vial. After partially evaporation the insoluble byproducts were rinsed with tetrahydrofuran (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial and the resulting solid was triturated with diethyl ether to give an off-white solid. (0.168 g, 59%) ¹H NMR (400 MHz, CD₃OD) δ 8.02 (dddd, J=2, 4.4, 7.2 and 8.4 Hz, 1H), 7.80 (dd, J=2 and 6.8 Hz, 1H), 7.62 (q, J=8 and 14.4 Hz, 1H), 7.34 (t, J=8.8 Hz, 1H), 7.04 (m, 2H), 6.69 (s, 1H), 5.36 (s, 2H), 3.29 (s, 3H), 1.98 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −108.94 (1F), −113.55 (1 F), −117.76 (1 F) ppm. ES-HRMS m/z 437.0861 (M+H calcd for C₂₁H₁₇ClF₃N₂O₃ requires 437.0874).

Examples 509-518

By following the method of Example 508 and replacing N-methylamine with the appropriate amine, the compounds of Examples 509-518 are prepared.

			%		M + H	ESHRMS
Example No.	R1	R2	Yield	MF	Requires	m/z
Ex. 509	CH3	CH3	59	C22H19ClF3N2O3	451.1031	451.1016
Ex. 510	H	CH2CH2OH	70	C22H19ClF3N2O4	467.0980	467.0985
Ex. 511	CH2CH2N(CH3)—	CH2CH2N(CH3)—	70	C25H24ClF3N3O3	506.1453	506.1447
Ex. 512	CH2CH2O—	CH2CH2O—	19	C24H21ClF3N2O4	493.1101	493.1136
Ex. 513	H	CH2CH2OCH3	59	C23H21ClF3N2O4	481.1136	481.1136
Ex. 514	CH3	CH2CH2OH	63	C23H21ClF3N2O4	481.1136	481.1131
Ex. 515	H	CH2CH2CH2OH	51	C23H21ClF3N2O4	481.1136	481.1121
Ex. 516	H	CH2CH(OH)CH2OH	64	C23H21ClF3N2O5	497.1086	497.1102
Ex. 517	H	C(CH3)2CH2OH—	54	C24H23ClF3N2O4	495.1293	495.1303
Ex. 518	CH2CH2NH—	CH2CH2NH—	34	C23H22ClF3N3O3	491.89

Example 519

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic Acid

Step 1 Preparation of methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoate

A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoate (7.3 g, 18 mmol) and N-methyl-2-pyrrolidine (20 mL). N-Bromo succinimide (3.5 g, 19.8 mmol) was added and the reaction mixture was stirred at room temperature for 30 minutes. The mixture poured into saturated aqueous NaHCO₃ and extracted with ethyl acetate. The organic layer was washed with brine, dried with Na₂SO₄, and concentrated in vacuo. The residue was triturated with diethyl ether and filtered to give the title compound as a white powder (3.49 g). ¹H NMR (400 MHz, CD₃OD) δ 8.16 (qd, J=3, 6.8 and 15.6 Hz, 1H), 7.84 (d, J=2.12 Hz, 1H), 7.64 (q, J=8.4 and 14.8 Hz, 1H), 7.29 (d, J=8.4 Hz, 1H), 7.04 (m, 2H), 6.60 (s, 1H), 5.34 (s, 2H), 3.87 (s, 3H), 2.00 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.51 (1F), −115.98 (1F), −117.43 (1F) ppm. ES-HRMS m/z 494.0387 (M+H calcd for C₂₂H₁₉BrF₂NO₅ requires 494.0409).

Step 2 Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid

A 100 mL round bottomed flask was charged with the product of Step 2 (3.4 g, 7.05 mmol), tetrahydrofuran (40 mL), methanol (10 mL), and water (10 mL). To this slurry was added 2.5 N NaOH (5.6 mL, 14.1 mmol). The reaction mixture became clear after 5 minutes and the reaction was complete in 1 h by LC-MS. The organics were removed on the rotary evaporator and the remaining solution was acidified to pH 1-2 with 6N HCl. The desired compound was precipitated by the addition of water and diethyl ether and subsequent filtration. The title compound was isolated as a white powder (2.64 g, 80%). ¹H NMR (400 MHz, CD₃OD) δ 8.21 (dddd, J=2.4, 5.2, 7.2 and 9.2 Hz, 1H), 8.00 (dd, J=2.0 and 7.2 Hz, 1H), 7.65 (q, J=8.4 and 14.8 Hz, 1H), 7.45 (t, J=8.4 Hz, 1H), 7.04 (appt, J=9.6 Hz, 1H), 6.65 (s, 1H), 5.36 (s, 2H), 2.07 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.40 (1F), −116.00 (1 F), −118.36 (1 F) ppm. ES-HRMS m/z 480.0259 (M+H calcd for C₂₁H₁₇BrF₂NO₅ requires 480.0253).

Example 520

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methoxybenzoic Acid

Step 1 Preparation of Methyl 3-amino-4-methoxybenzoate

A 1 L 3-necked round bottomed flask equipped with a nitrogen inlet, stirbar, addition funnel and thermocouple was charged with 3-amino-4-methoxy benzoic acid (50 g, 0.299 mol) and methanol (300 mL). The system was cooled to 0 C and acetyl choride (30 mL, 0.42 mol) was added dropwise. The system was warmed to room temperature, the addition funnel was replaced with a reflux condensor, and was heated to reflux for 1.5 h. The reaction mixture was cooled to room temperature, quenched with saturated aqueous NaHCO₃, and extracted with ethyl acetate. The organic extract was washed with brine, dried with Na₂SO₄ and concentrated in vacuo to give methyl 3-amino-4-methoxybenzoate as a dark solid (47.9 g, 88%). ¹H NMR (400 MHz, CD₃OD) δ 7.40 (t, J=2 68 Hz, 1H), 7.37 (t, J=2.0 Hz, 1H), 6.86 (d, J=8.8 Hz, 1H), 3.98 (s, 3H), 3.81 (s, 3H) ppm. ES-HRMS m/z 182.0826 (M+H calcd for C₉H₁₂ClNO₃ requires 182.0812).

Step 2 Preparation of Methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-methoxybenzoate

A 250 mL round bottomed flask equipped with stirbar, Dean-Stark trap and reflux condensor was charged with the product of Step 1(23.5 g, 0.129 mol), 4-hydroxy-6-methyl-2-pyrone (17.8 g, 0.14 mol), and o-dichlorobenzene (200 mL). The system was immersed in a 170 C oil bath for 2 h and was then cooled to room temperature. The reaction mixture was washed with aqueous Na₂CO₃ (28 g, 0.26 mol, 500 mL water). The aqueous layer was washed with ethyl acetate and then was acidified to pH 1-2 with concentrated HCl. This was extracted with ethyl acetate, which was then dried with Na₂SO₄ and concentrated in vacuo. The viscous orange oil was triturated with MeOH to give the title compound as a yellow solid (1.61 g, 4%). ¹H NMR (400 MHz, CD₃OD) δ 8.14 (dd, J=2.2 and 8.8 Hz, 1H), 7.79 (d, J=2.2 Hz, 1H), 7.27 (d, J=8.8 Hz, 1H), 6.05 (d, J=2.3 Hz, 1H), 5.77 (d, J=2.3 Hz, 1H), 3.88 (s, 3H), 3.87 (s, 3H), 1.90 (s, 3H) ppm. ES-HRMS m/z 290.0997 (M+H calcd for C₁₅H₁₆NO₅ requires 290.1023).

Step 3 Preparation of Methyl 3-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methoxybenzoate

A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the product of Step 2 (1.6 g, 5.5 mmol) and N,N-dimethyl formamide (10 mL). 1,8-diazabicyclo[5.4.0]undec-7-ene (0.91 mL, 6 mmol) was added followed by 2,4-difluorobenzyl bromide (0.77 mL, 6 mmol). The reaction mixture was stirred at 60 C for 4 h, was poured into saturated aqueous NaHCO₃ and was extracted with ethyl acetate. The organic layer was washed with brine, dried with Na₂SO₄ and concentrated in vacuo to give the title compound as an orange foam (2.13 g, 93%), which was carried on to the next reaction without further purification. ¹H NMR (400 MHz, CD₃OD) δ 8.17 (dd, J=2.64 and 11.6 Hz, 1H), 7.82 (td, J=2.7 and 6.8 Hz, 1H), 7.57 (m, 1H), 7.29 (d, J=11.6 Hz, 1H), 7.02 (m, 2H), 6.16 (m, 1H), 6.03 (d, J=3.5 Hz, 1H), 5.14 (s, 2H), 3.89 (s, 6H), 1.93 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.43 (1F), −116.04(1 F) ppm. ES-HRMS m/z 416.1310 (M+H calcd for C₂₂H₂₀F₂NO₅ requires 416.1304).

Step 4 Preparation of Methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methoxybenzoate

A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the product of Step 3 (2.1 g, 5.06 mmol) and N-methyl-2-pyrrolidine (10 mL). N-Bromo succinimide (1 g, 5.56 mmol) was added and the reaction mixture was stirred at room temperature for 1 h. The mixture poured into saturated aqueous NaHCO₃ and extracted with ethyl acetate. The organic layer was washed with brine, dried with Na₂SO₄, and concentrated in vacuo. The residue was chromatographed on silica (1:1 hexanes: ethyl acetate) to give the title compound as an orange oil (0.77 g, 31%). ¹H NMR (400 MHz, CD₃OD) δ 8.16 (app qd, J=2.5 and 7.2 Hz, 1H), 7.84 (d, J=2.6 Hz, 1H), 7.64 (m, 1H), 7.30 (d, J=9.2 Hz, 1H), 7.04 (appt, J=8.4 Hz, 2H), 6.60 (s, 1H), 5.33 (s, 2H), 3.80 (s, 6H), 1.99 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.56 (1F), −116.00 (1 F) ppm. ES-HRMS m/z 494.0398 (M+H calcd for C₂₂H₁₉BrF₂NO₅ requires 494.0409).

Step 5 Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]4-methoxybenzoic Acid

A 100 mL round bottomed flask was charged with the product of Step 4 (0.77 g, 1.55 mmol), tetrahydrofuran (10 mL), methanol (5 mL), and water (5 mL). To this slurry was added 2.5 N NaOH (1.2 mL, 3.1 mmol). The reaction mixture became clear after 30 minutes and the reaction was complete in 1 h by LC-MS. The organics were removed on the rotary evaporator and the remaining solution was acidified to pH 2-3 with 6N HCl. The desired compound was precipitated by the addition of water and diethyl ether and subsequent filtration. The title compound was isolated as a white powder (0.60 g, 81%). ¹H NMR (400 MHz, CD₃OD) δ 8.17 (dd, J=2.2 and 8.8 Hz, 1H), 7.82 (d, J=2.2 Hz, 1H), 7.64 (q, 1H), 7.29 (d, J=8.8 Hz, 1H), 7.34 (t, J=8.8 Hz, 2H), 6.60 (s, 1H), 5.34 (s, 2H), 3.87 (s, 3H), 2.01 (s, 3H) ppm. ES-HRMS m/z 480.0259 (M+H calcd for C₂₁H₁₇BrF₂NO₅ requires 480.0253).

Example 521

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methoxy-N-methylbenzamide

Step 1

To a reaction vessel (borosilicate culture tube) was added Example 520 (0.300 g, 0.624 mmol) and 1-hydroxybenzotriazole (0.042 g, 0.31 mmol). N,N-Dimethylformamide (3 mL) was added to the reaction vessel followed by approximately 1.06 g of the polymer bound carbodiimide resin (1.38 mmol/g). Additional N,N-dimethylformamide (2 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. N-Methyl amine (2 mL, 4 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with tetrahydrofuran (20 mL) and treated with approximately 2 g of polyamine resin (2.63 mmol/g) and approximately 2.5 g of methylisocyanate functionalized polystyrene (1.5 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 3 hours. The reaction vessel was then opened and the solution phase product was separated from the insoluble quenched byproducts by filtration and collection into a vial. After partially evaporation the insoluble byproducts were rinsed with tetrahydrofuran (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial and the resulting solid was triturated with diethyl ether to give the desired product as an off-white solid (0.094 g, 31%). ¹H NMR (400 MHz, CD₃OD) δ 7.98 (dd, J=2.2 and 8.8 Hz, 1H), 7.64 (m, 2H), 7.28 (d, J=9.2 Hz, 1H), 7.04 (t, J=9.2 Hz, 2H), 6.60 (s, 1H), 5.34 (s, 2H), 3.86 (s, 3H), 2.88 (s, 3H), 2.01 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.59 (1F), −116.01 (1 F) ppm. ES-HRMS m/z 493.0593 (M+H calcd for C₂₂H₂₀BrF₂N₂O₄ requires 493.0569).

Example 522

Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methoxy-N,N-dimethylbenzamide

The title compound was prepared essentially as in Example 521. ¹H NMR (400 MHz, CD₃OD) δ 7.64 (m, 1H), 7.61 (dd, J=2 and 8.8 Hz, 1H), 7.33 (d, J=2.2 Hz, 1H), 7.27 (d, J=8 Hz, 1H), 7.04 (t, J=8 Hz, 2H), 6.59 (s, 1H), 5.33 (s, 2H), 3.85 (s, 3H), 3.07 (s, 6H), 2.02 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.60 (1F), −116.01 (1 F) ppm. ES-HRMS m/z 507.0716 (M+H calcd for C₂₃H₂₂BrF₂N₂O₄ requires 507.0726).

Example 523

1-[5-(aminomethyl)-2-fluorophenyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Hydrochloride

Step 1

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzamide

A 250 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid (2.58 g, 6.1 mmol), 4-methylmorpholine (2.0 mL, 18.3 mmol), 2-chloro-4,6-dimethoxy-1,3,5-triazine (1.28 g, 7.3 mmol) and tetrahydrofuran (30 mL). After stirring the mixture for 30 min at 250 C, NH₄OH (15.0 mL) was added. The mixture was stirred for 30 min and diluted with water. The product precipitated from solution. The precipitated was filtered and washed with water and diethyl ether to give the title compound (2.55 g, 78%) as a white solid. ¹H NMR (400 MHz, (CD₃)₂SO) δ 8.10 (m, 1H), 7.9 (dd, J=2.1 and 5.2 Hz, 1H), 7.65 (q, 6.7 and 8.5 Hz, 1H), 7.56 (t, J=9.1 Hz, 1H), 7.35 (td, J=2.4 and 8.2 Hz, 1H) 7.17 (td, J=2 and 6.6 Hz, 1H) 6.78 (s, 1H), 5.36 (s, 2H), 2 (s, 3H) ppm. ES-HRMS m/z 423.0719 (M+H calcd for C₂₀H₁₅ClF₃N₂O₃ requires 423.0718).

Step 2

Preparation of 1-[5-(aminomethyl)-2-fluorophenyl]-3-chloro-4-[(2,4 difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Hydrochloride

A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the product from step 1(1.5 g, 3.5 mmol), BH₃.THF complex (7.4 mL, 7.4 mmol), and tetrahydrofuran (15 mL). The mixture was refluxed for 6 h, allowed to cool to room temperature and quenched with HCl 6N. The organics were evaporated and the remaining aqueous solution was saturated with NaOH 2.5N and extracted with dichloromethane. The organic phase was dried with Na₂SO₄ and concentrated in vacuo. HCl 6N was added, and concentrated in vacuo. ¹H NMR (400 MHz, (CD₃)₂SO) δ 8.2 (m, 1H), 7.6 (m, 1H), 7.5 (m, 1H), 7.3 (t, J=9.8 Hz, 1H), 7.16 (t, J=8.6 Hz, 1H) 6.78 (s, 1H), 5.36 (s, 2H), 4.05 (d, J=5.8 Hz, 2H), 2 (s, 3H) ppm. ES-HRMS m/z 409.0940 (M+H calcd for C₂₀H₁₇ClF₃N₂O₂ requires 409.0925).

Example 524

3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluoro-N-[2-hydroxy-1-(hydroxymethyl)ethyl]benzamide

Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluoro-N-[2-hydroxy-1-(hydroxymethyl)ethyl]benzamide

The title compound was prepared essentially as in Example 521. ¹H NMR (400 MHz, CD₃OD) δ 8.1 (m, 1H), 7.8 (dd, J=2.3 and 5.1 Hz, 1H), 7.6 (q, J=7.4 and 7.0 Hz, 1H), 7.41 (t, J=8.9 Hz, 1H), 7.04 (m, 2H) 6.7 (s, 1H), 5.36 (s, 2H), 4.1 (t, J=5.8 Hz, 1H), 3.7 (d, J=5.1 Hz, 4H) 2.1 (s, 3H) ppm. ES-HRMS m/z 497.1045 (M+H calcd for C₂₃H₂₁ClF₃N₂O₅ requires 497.1086).

Examples 525-528

The compounds of Examples 525-528 are prepared by derivitazion of Example 523. The analytical data are shown below.

			M+H	ESHRMS
Ex. No.	R	MF	Requires	m/z
Ex. 525	—C(O)CH3	C22H18ClF3N2O3	451.1031	451.1010
Ex. 526	—C(O)CH2OCH3	C23H20ClF3N2O4	481.1136	481.1132
Ex. 527	—SO2CH3	C21H18ClF3N2O4S	487.0701	487.0679
Ex. 528	—C(O)NH2	C21H16ClF3N3O3	452.0983	452.0987

NMR characterization of compounds of Examples 525-528

Ex. No. NMR Data
525     1H NMR (400MHz, CD3OD) δ 7.6(q, J=7.8 and 7.0Hz, 1H), 7.5(m, 1H), 7.3(t, J=9.0Hz,
        1H), 7.2(dd, J=1.9 and 5.1Hz, 1H), 7.05(m, 2H), 6.65(s, 1H), 5.36(s, 2H), 4.39(s, 2H), 2.1
        (s, 3H), 1.98(s, 3H) ppm
526     1H NMR (400MHz, CD3Cl3) δ 7.45(q, J=8.6 and 6.2Hz, 1H), 7.3(m, 1H), 7.1(m, 2H), 6.85
        (q, J=6.5 and 1.9Hz, 1H), 6.78(td, J=2.7 and 7.8Hz, 1H), 6.2(s, 1H), 5.2(s, 2H), 4.39(d, J =
        6.2 Hz, 2H), 4.0(s, 3H) 2.3(s, 2H), 2.0(s, 3H), 1.98(s, 3H) ppm
527     1H NMR (400MHz, CD3OD) δ 7.49(q, J=8.2 and 6.3Hz, 1H), 7.33(m, 1H), 7.23(m, 1H), 7.1
        (t, J=8.9, 1H), 6.9(td, J=0.78 and 6.6 1H), 6.8(td, J=2.7 and 6.25Hz, 1H), 6.2(s, 1H), 5.2(s,
        2H), 4.2(s, 2H), 2.8(s, 3H) 2.0(s, 3H) ppm
528     1H NMR (400MHz,(CD3)2SO) δ 7.61(q, J=8.9 and 6.6Hz, 1H), 7.38(d, J=7.8Hz, 1H), 7.3
        (d, J=10.2Hz, 1H) 7.21(d, J=7.4Hz, 1H), 7.1(t, J=8.6Hz, 1H), 6.71(s, 1H), 6.5(t, J=5.8Hz,
        1H), 5.56(s, 2H), 5.3(s, 2H), 4.18(d, J=6.25Hz, 2H), 3.61(s, 1H), 1.98(s, 3H) ppm

Example 529

2-({[3-chloro-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzonitrile

2-(bromomethyl)-5-fluorobenzonitrile (3.47 g, 16.2 mmol), 3-chloro-1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (3.15 g, 11.6 mmol), K₂CO₃ (2.56 g, 18.6 mmol), and 18-crown-6 (0.15 g) were dissolved in N,N-dimethylacetamide (25 mL). Reaction mixture stirred on 60° C. oil bath for 4 hours. Solvent removed by distillation. Reaction neutralized with 5% citric acid. The solid product was washed with hexane followed by 30% EtOAc/hexane. Filtered a brown solid (5.2 g, 79% yield). ¹H NMR (CD₃OD/400 MHz) δ 7.82 (m, 2H), 7.61 (m, 4H), 6.75 (s, 1H), 5.49 (s, 2H), 2.13 (s, 3H). ESHRMS m/z 405.0616 (M+H C₂₀H₁₃ClF₃N₂O₂ requires 405.0612).

Example 530

4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-chloro-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one Trifluoroacetate

BH₃THF (17.8 mL, 17.8 mmol) was added dropwise to a chilled (0° C.) solution of 2-({[3-chloro-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzonitrile (3.61 g, 8.92 mmol) in THF (30 mL). Following the addition, the reaction was heated at 60° C. for 1.5 hours. The reaction was quenched with MeOH, the solvent evaporated, and the crude product purified by prep HPLC. The product was isolated by freeze-drying and evaporation of the solvent to give a white solid (1.52 g, 32.6%). ¹H NMR (CD₃OD/400 MHz) δ 7.62 (m, 2H), 7.32 (m, 1H), 7.25 (tr, 2H, J=8.00 Hz), 7.18 (m, 1H), 6.78 (s, 1H), 5.43 (s, 1H), 4.22 (s, 1H), 2.14 (s, 3H). ESHRMS m/z 409.0900 (M+H C₂₀H₁₇N₂O₂F₃Cl requires 409.0925).

Examples 531-551

The compounds of Examples 531-551 are prepared by derivitazion of Example 530. The analytical data are shown below.

Compound			M + H	ESHRMS
No.	R	MF	Requires	m/z
Ex. 531	—OCH3	C22H18ClF3N2O4	467.0980	467.0985
Ex. 532	—CF3	C22H15ClF6N2O3	505.0748	505.0754
Ex. 533	—O-isopropyl	C24H22ClF3N2O4	495.1293	495.1304
Ex. 534	—NH—CH2CH3	C23H21ClF3N3O3	480.1296	480.1277
Ex. 535	—O-tetrahydrofuran-3-yl	C25H22ClF3N2O5	523.1242	523.1282
Ex. 536	—O-propyl	C24H22ClF3N2O4	495.1293	495.1338
Ex. 537	—O—CH2CH═CH2	C24H20ClF3N2O4	493.1136	493.1116
Ex. 538	—O—CH2C≡CH	C24H18ClF3N2O4	491.0980	491.0961
Ex. 539	—O-tButyl	C25H24ClF3N2O4	509.1449	509.1436
Ex. 540	—NH-tButyl	C25H25ClF3N3O3	508.1609	508.1574
EX. 541	—SO2CH2CH2CH3	C23H22ClF3N2O4S	515.1014	515.0979
Ex. 542	—SO2CH2CH3
Ex. 543	—NH-isopropyl	C24H23ClF3N3O3	494.1453	494.1456
Ex. 544	—CH2OCH3	C23H20ClF3N2O4	481.1136	481.1174
Ex. 545	—NHCH3	C22H20ClF3N3O3	466.1140	466.1141
Ex. 546	—N(CH3)(tButyl)	C26H27ClF3N3O3	522.1766	522.1737
Ex. 547	—NH(cyclopropyl)	C24H21ClF3N3O3	492.1296	492.1285
Ex. 548	—NHCH2CF3	C23H17ClF6N3O3	534.1014	534.1005
Ex. 549	NHCH2(cyclopropyl)	C25H23ClF3N3O3	506.1453	506.1432
Ex. 550	—NHCH2(tButyl)	C26H27ClF3N3O3	522.1766	522.1740
Ex. 551	—N(CH3)2	C23H22ClF3N3O3	480.1296	480.1307

NMR characterization of compounds of Examples 531-551

Ex. No. NMR data
531     1H NMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.53(m, 1H), 7.24(t, 2H, J=8.00Hz), 7.14(m,
        1H), 7.05(m, 1H), 6.74(s, 1H), 5.40(s, 2H), 4.42(s, 2H), 3.63(s, 3H), 2.12(s, 3H)
532     1H NMR(CD3OD/400MHz) δ 7.59(m, 2H), 7.24(t, 2H, J=8.00Hz), 7.11(m, 2H), 6.73(s,
        1H), 5.43(s, 2H), 4.62(s, 2H), 2.12(s, 3H)
533     1H NMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.53(m, 1H), 7.24(t, 2H, J=7.60Hz), 7.13
        (m, 1H), 7.05(m, 1H), 6.74(s, 1H), 5.40(s, 2H), 4.81(m, 1H), 4.41(s, 2H), 2.12(s, 3H),
        1.21(d, 6H, J=6.00Hz)
534     1H NMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.52(m, 1H), 7.24(t, 2H, J=0.80Hz), 7.13
        (m, 1H), 7.03(m, 1H), 6.73(s, 1H), 5.39(s, 2H), 4.44(s, 2H), 3.12(q, 2H, J=7.20Hz), 2.12
        (s, 3H), 1.08(t, 3H, J=7.20Hz)
535     1H NMR(CD3OD/300MHz) δ 7.62(m, 1H), 7.54(m, 1H), 7.25(t, 2H, J=8.4Hz), 7.15(m,
        1H), 7.07(m, 1H), 6.75(s, 1H), 5.41(s, 2H), 5.15(s br, 1H), 4.44(s, 2H), 3.82(m, 4H),
        2.13(s, 4H), 2.03(s br, 1H)
536     1H NMR(CD3OD/300MHz) δ 7.62(m, 1H), 7.54(m, 1H), 7.25(t, 2H, J=8.1Hz), 7.15(m,
        1H), 7.06(m, 1H), 6.74(s, 1H), 5.41(s, 2H), 4.43(s, 2H), 3.98(t, 2H, J=6.6Hz), 2.13(s,
        3H), 1.63(m, 2H), 0.94(t, 3H, J=7.2Hz)
537     1H NMR(CD3OD/300MHz) δ 7.62(m, 1H), 7.54(m, 1H), 7.25(t, 2H, J=8.4Hz), 7.14(m,
        1H), 7.07(m, 1H), 6.74(s, 1H), 5.92(m br, 1H), 5.41(s, 2H), 5.29(d, 1H, J=17.7Hz), 5.17
        (d, 1H, J=10.5Hz), 4.63(s, 1H), 4.53(d, 2H, J=5.4Hz), 4.44(s, 2H), 2.13(s, 3H)
538     1H NMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.53(m, 1H), 7.24(t, 2H, J=7.6Hz), 7.14(m,
        1H), 7.06(m, 1H), 6.74(s, 1H), 5.41(s, 2H), 4.65(d, 2H, J=2.4Hz), 4.44(s, 2H), 2.86(t,
        1H, J=2.4Hz), 2.12(s, 3H)
539     1H NMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.53(m, 1H), 7.24(tr, 2H, J=8.40), 7.12(m,
        1H), 7.05(m, 1H), 6.74(s, 1H), 5.39(s, 2H), 4.36(s, 2H), 2.12(s, 3H), 1.43(s, 9H)
540     1H NMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.53(m, 1H), 7.24(tr, 2H, J=8.00Hz), 7.12
        (m, 1H), 7.04(m, 1H), 6.73(s, 1H), 5.37(s, 2H), 4.39(s, 2H), 2.12(s, 3H), 1.28(s, 9H)
541     1H NMR(CD3OD/300MHz) δ 7.59(m, 2H), 7.26(m, 3H), 7.11(m, 1H), 6.75(s, 1H), 5.46
        (s, 2H), 4.40(s, 2H), 3.02(m, 2H), 2.12(s, 3H), 1.80(m, 2H), 1.03(tr, 3H, J=7.50MHz)
542     1H NMR(CD3OD/400MHz) δ 7.58(m, 2H), 7.26(m, 3H), 7.10(m, 1H), 6.74(s, 1H), 5.45
        (s, 2H), 4.39(s, 2H), 3.06(q, 2H, J=7.60Hz), 2.11(s, 3H), 1.31(t, 3H, J=7.2Hz)
543     1H NMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.52(m, 1H), 7.24(t, 2H, J=8.40Hz), 7.12
        (m, 1H), 7.04(m, 1H), 6.73(s, 1H), 5.39(s, 2H), 4.44(s, 2H), 3.77(m, 1H), 2.12(s, 3H),
        1.10(d, 6H, J=6.40Hz)
544     1H NMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.54(m, 1H), 7.24(t, 2H, J=7.6Hz), 7.15(m,
        1H), 7.06(m, 1H), 6.74(s, 1H), 5.43(s, 2H), 4.55(s, 2H), 3.92(s, 2H), 3.40(s, 3H), 2.12(s,
        3H)
545     1H NMR(CD3OD/300MHz) δ 7.63(m, 1H), 7.54(m, 1H), 7.26(t, 2H, J=8.7Hz), 7.15(m,
        1H), 7.05(m, 1H), 6.75(s, 1H), 5.42(s, 2H), 4.47(s, 2H), 2.70(s, 3H), 2.14(s, 3H)
546     1H NNMR(CD3OD/300MHz) δ 7.63(m, 1H), 7.53(m, 1H), 7.25(t, 2H, J=9.0Hz), 7.14
        (m, 1H), 7.04(m, 1H), 6.76(s, 1H), 5.41(s, 2H), 4.44(s, 2H), 2.90(s, 3H), 2.13(s, 3H),
        1.39(s, 9H)
547     1H NNMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.52(m, 1H), 7.24(t, 2H, J=7.6Hz), 7.14
        (m, 1H), 7.03(m, 1H), 6.74(s, 1H), 5.41(s, 2H), 4.47(s, 2H), 2.46(m, 1H), 2.12(s, 3H),
        0.68(q, 2H, J=5.2Hz), 0.46(m, 2H)
548     1H NNMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.53(m, 1H), 7.24(t, 2H, J=8.0Hz), 7.12
        (m, 1H), 7.04(m, 1H), 6.73(s, 1H), 5.39(s, 2H), 4.47(s, 2H), 3.79(q, 2H, J=9.6Hz), 2.12
        (s, 3H)
549     1H NNMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.52(m, 1H), 7.24(t, 2H, J=8.4Hz), 7.14
        (m, 1H), 7.04(m, 1H), 6.73(s, 1H), 5.39(s, 2H), 4.45(s, 2H), 2.96(d, 2H, J=6.8Hz), 2.12
        (s, 3H), 0.93(m, 1H), 0.44(m, 2H), 0.16(q, 2H, J=4.8Hz)
550     1H NNMR(CD3OD/400MHz) δ 7.61(m, 1H), 7.53(m, 1H), 7.24(t, 2H, J=8.0Hz), 7.14
        (m, 1H), 7.04(m, 1H), 6.73(s, 1H), 5.39(s, 2H), 4.46(s, 2H), 2.92(d, 2H, J=4.8Hz), 2.12
        (s, 3H), 0.87(s, 9H)
551     1H NNMR(CD3OD/300MHz) δ 7.62(m, 1H), 7.52(m, 1H), 7.25(t, 2H, J=8.7Hz), 7.15
        (m, 1H), 7.04(m, 1H), 6.75(s, 1H), 5.42(s, 2H), 4.48(s, 2H), 2.90(s, 6H), 2.14(s, 3H)

Example 552

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(1-hydroxy-1-methylethyl)pyridin-2-yl]methyl}-6-methylpyridin-2(1H)-one

Step 1: Preparation of Methyl 6-methylnicotinate 1-oxide.

Methyl 6-methylnicotinate (6.0 g, 39.7 mmol) was added into dichloromethane (100 mL) in the round bottom flask under nitrogen. 3-chloroperoxybenzoic acid (10.0 g, 57.9 mmol) was then added into the flask and stirred for 5 hour. Saturated sodium bicarbonate solution (100 ml) was added into the reaction and the mixture was transferred to separatory funnel. Additional 200 mL of dichloromethane was added into the funnel and obtained the organic layer. The organic layer was washed with water (150 mL) and dried over anhydrous magnesium sulfate. The resulting solution was evaporated to yield white solid (6 g, 90%). LC/MS, t_r=0.33 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 168 (M+H). ES-HRMS m/z 168.0628 (M+H calcd for C₈H₁₀NO₃ requires 168.0655).

Step 2: Preparation of Methyl 6-(Chloromethyl)nicotinate

Methyl 6-methylnicotinate 1-oxide (from Step 1) (6.0 g, 35.9 mmol) was was added into the p-toluenesulfonyl chloride (10 g, 52.4 mmol) in 100 mL of 1,4-dioxane. The mixture was heated to reflux for 20 hours. Saturated sodium bicarbonate solution (200 ml) was added into the reaction and the mixture was transferred to separatory funnel. The compound was extracted using ethyl acetate (300 ml×2) and the combined ethyl acetate solution was dried over magnesium sulfate and evaporated to black solid (5.2 g, 78%). LC/MS, t_r=1.52 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 186 (M+H). ES-HRMS m/z 186.0314 (M+H calcd for C₈H₉ClNO₂ requires 186.0316).

Step 3: Preparation of Methyl 6-{[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinate

Methyl 6—(Chloromethyl)nicotinate (from step 2). (2 g, 10.8 mmol) was added into 4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one in 20 mL of dimethyl formamide followed by addition of cesium carbonate (5 g, 15.3 mmol). The mixture was heated to 100 C for 20 hours. It was cooled to room temperature and added 400 mL of water. Brown precipitate came out of from solution. It was filtered and rinsed with water (200 mL×3) and dried to obtain 4 g of solid. The product was purified using a Gilson Reversed Phase preparative chromatography to obtain white solid (1.4 g, 32%). ¹H NMR (400 MHz, CDCl₃) δ 9.09 (d, J=1.48 Hz, 1H), 8.19 (dd, J=6.04, 2.15 Hz, 1H), 7.37 (app q, J=8.32 Hz, 1H), 7.25 (d, J=8.33 Hz, 1H), 6.84 (m, 2H), 5.94 (d, J=2.82 Hz, 1H), 5.83 (d, J=2.15 Hz, 1H), 5.36 (s, 2H), 4.97 (s, 2H), 3.90 (s, 3H), 2.27 (s, 3H); LC/MS, t_r=2.30 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 401 (M+H). ES-HRMS m/z 401.1307 (M+H calcd for C₂₁H₁₉F₂N₂O₄ requires 401.1307).

Step 4: Preparation of the Title Compound

3 molar solution of methyl magnesium bromide in ether (5 mL, 15 mmol) was added into 5 ml of anhydrous tetrahydrofuran in the round bottom flaks under nitrogen. The mixture was cooled to 0° C. Methyl 6-{[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinate (from Step 3) (300 mg, 0.75 mmol) was dissolved in 5 ml of anhydrous tetrahydrofuran in dropper funnel and the solution was slowly added into cold methyl magnesium bromide solution in the round bottom flask. After the addition, the mixture was continue stirring at 0 C for 30 minute and cold solution of saturated ammonium chloride (100 ml) was added slowly into the reaction mixture. The mixture was transferred to separatory funnel and the product was extracted with ethyl acetate (200 ml×2). The combined ethyl acetate solution was dried over anhydrous magnesium sulfate and evaporated to dryness. The resulting residue (220 mg) was added into 10 ml of dichloromethane followed by addition of N-bromo succinimide (100 mg, 0.56 mmol). The solution was stirred at room temperature for 3 hours. Saturated sodium bicarbonate solution (100 ml) was added into the reaction mixture and it was transferred to separatory funnel. The product was extracted with ethyl acetate (200 ml×2). The combined ethyl acetate solution was dried over anhydrous magnesium sulfate and evaporated to dryness. ¹H NMR (400 MHz, CDCl₃) δ 8.61 (d, J=1.88 Hz, 1H), 7.73 (dd, J=5.77, 2.42 Hz, 1H), 7.55 (app q, J=6.31 Hz, 1H), 7.30 (d, J=8.19b Hz, 1H), 6.93 (m, 1H), 6.84 (m, 1H), 6.00 (s, 1H), 5.37 (s, 2H), 5.19 (s, 2H), 2.48 (s, 3H), 1.56 (s, 6H); LC/MS, t_r=2.29 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 m/min with detection 254 nm, at 50° C.). ES-MS m/z 479 (M+H). ES-HRMS m/z 479.0791 (M+H calcd for C₂₂H₂₂BrF₂N₂O₃ requires 479.0776).

Example 553

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyridin-2-yl]methyl}-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyridin-2-yl]methyl}-6-methylpyridin-2(1H)-one

Methyl 6-{[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinate (from preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(1-hydroxy-1-methylethyl)pyridin-2-yl]methyl}-6-methylpyridin-2(1H)-one, step 3) (350 mg, 0.87 mmol) was added into anhydrous tetrahydrofuran (15 ml) and the solution was cooled to −78 C. Into the cold solution, was added lithium aluminum hydride (100 mg, 2.6 mmol). After the addition, the reaction mixture was warm to 0 C and continue stirring for one additional hour. Potassium hydrogen sulfate (1 N solution, 150 ml) was added slowly into the reaction mixture to quench the reaction. The resulting mixture was transferred to a separatory funnel and the product was extracted with ethyl acetate (200 ml×2). The combine ethyl acetate solution was dried over anhydrous magnesium sulfate and evaporated to dryness. LC/MS, t_r=1.88 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 373 (M+H).

Step 2: Preparation of the Title Compound

4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyridin-2-yl]methyl}-6-methylpyridin-2(1H)-one (from step 1). (230 mg, 0.62 mmol) was added into 10 ml of dichloromethane followed by addition of N-bromo succinimide (110 mg, 0.62 mmol). The solution was stirred at room temperature for 3 hours. Saturated sodium bicarbonate solution (100 ml) was added into the reaction mixture and it was transferred to a separatory funnel. The product was extracted with ethyl acetate (200 ml×2). The combined ethyl acetate solution was dried over anhydrous magnesium sulfate and evaporated to dryness. ¹H NMR (400 MHz, CDCl₃) δ 8.47 (app s, 1H), 7.64 (dd, J=5.77, 2.29 Hz, 1H), 7.55 (app q, J=6.45 Hz, 1H), 7.33 (d, J=6.05 Hz, 1H), 6.93 (m, 1H), 6.84 (m, 1H), 6.00 (s, 1H), 5.39 (s, 2H), 5.19 (s, 2H), 4.68 (s, 2H), 2.46 (s, 3H); LC/MS, t_r=2.01 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 451 (M+H).

Example 554

6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)-N-methylnicotinamide

Step 1: Preparation of methyl 6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinate

Methyl 6-{[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinate (from preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(1-hydroxy-1-methylethyl)pyridin-2-yl]methyl}-6-methylpyridin-2(1H)-one, step 3) (350 mg, 0.87 mmol) (1.0 g, 2.5 mmol) was added into 150 ml of dichloromethane followed by addition of N-bromo succinimide (500 mg, 2.8 mmol). The solution was stirred at room temperature for 3 hours. Saturated sodium bicarbonate solution (300 ml) was added into the reaction mixture and it was transferred to a separatory funnel. The product was extracted with ethyl acetate (500 ml×2). The combined ethyl acetate solution was dried over anhydrous magnesium sulfate and evaporated to dryness. ¹H NMR (400 MHz, CDCl₃) δ 9.08 (app d, J=2.15 Hz, 1H), 8.21 (dd, J=6.04, 2.15 Hz, 1H), 7.55 (app qt, J=6.31 Hz, 1H), 7.41 (d, J=6.31 Hz, 1H), 6.91 (m, 1H), 6.84 (m, 1H), 6.02 (s, 1H), 5.42 (s, 2H), 5.19 (s, 2H), 3.91 (s, 3H), 2.45 (s, 3H); LC/MS, t_r=2.85 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 m/min with detection 254 nm, at 50° C.). ES-MS m/z 479 (M+H). ES-HRMS m/z 479.0415 (M+H calcd for C₂₁H₁₈BrF₂N₂O₄ requires 479.0413).

Step 2: Preparation of 6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinic Acid

Methyl 6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinate (from step 1) (1.0 g, 2.1 mmol) was added into the mixture of 100 ml tetrahydrofuran and 10 ml of methanol followed by addition of 2.5 N sodium hydroxide (0.85 ml, 2.1 mmol). The solution was heated to 50 C for 2 hours. After the solution was cooled to room temperature and evaporate to completely dried residue. The residue was added into 50 ml of tetrahydrofuran and 4 N HCl in 1,4-dioxane (0.52 ml, 2.1 mmol) and stirred the mixture for 30 minute. The mixture was evaporate to dryness. The residue was added 20 ml water and the aqueous solution was neutralized to exactly ph 7 by addition of saturated sodium bicarbonate solution drop wise. The resulting heterogeneous mixture was left standed for 20 hours. Filtered, rinsed with water (30 ml×3) and dried over high vacuum oven to afford white solid (950 mg, 97%). ¹H NMR (400 MHz, CDCl₃ and CD₃OD) δ 8.98 (app br s, 1H), 8.15 (dd, J=6.17, 2.02 Hz, 1H), 7.45 (app q, J=6.58 Hz, 1H), 7.21 (d, J=8.19 Hz, 1H), 6.84 (m, 1H), 6.76 (m, 1H), 6.04 (s, 1H), 5.35 (s, 2H), 5.12 (s, 2H), 2.32 (s, 3H); LC/MS, t_r=2.48 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 465 (M+H). ES-HRMS m/z 465.0254 (M+H calcd for C₂₀H₁₆BrF₂N₂O₄ requires 465.0256).

Step 3: Preparation of the Title Compound

6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinic acid (from step 2)(230 mg, 0.5 mmol) was added into the 1-hydroxybenzotriazole (101 mg, 0.75 mmol) in 5 ml of N,N-dimethylforamide. 4-methyl morpholine (0.16 ml, 1.5 mmol) was added into the mixture followed by addition of 1-(3-(dimethylamino)propyl-3-ethylcarbodiimide hydrochloride (143 mg, 0.75 mmol). Stirred the mixture for 30 minute to become homogenous solution. To that homogenous solution, was added 2-(methylamino)ethanol (0.06 ml, 0.75 mmol) and the mixture was stirred for 20 hours. Water (150 ml) was added into the reaction mixture and the product was extracted using ethyl acetate (400 ml×2). The combined ethyl acetate solution was dried over anhydrous magnesium sulfate and evaporated to dryness. ¹H NMR (400 MHz, DMSO-d₆) δ 8.47 (app br s, 1H), 7.80 (br d, J=7.92 Hz, 1H), 7.64 (app q, J=6.58 Hz, 1H), 7.30 (m, 2H), 7.15 (m, 1H), 6.56 (s, 1H), 5.39 (s, 2H), 5.28 (s, 2H), 3.46 (m, 2H), 3.23 (m, 2H) 2.93 (m, 3H), 2.36 (s, 3H); LC/MS, t_r=2.29 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-HRMS m/z 522.0850 (M+H calcd for C₂₃H₂₃BrF₂N₃O₄ requires 522.0835).

Example 555

6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)nicotinamide

Following the method of Example 554 (step 3) and substituting 2-(methylamino)ethanol for the ethanolamine obtained the title compound as a white solid (79% yield). ¹H NMR (400 MHz, CD₃OD) δ 8.93 (d, J=2.01 Hz, 1H), 8.21 (dd, J=6.04, 2.21 Hz, 1H), 7.67 (app q, J=6.44 Hz, 1H), 7.39 (d, J=8.06 Hz, 1H), 7.08 (m, 2H), 6.58 (s, 1H), 5.55 (s, 2H), 5.35 (s, 2H), 3.74 (app t, J=5.73 Hz, 2H), 3.53 (app t, J=5.73 Hz, 2H), 2.49 (s, 3H); LC/MS, t_r=2.26 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-HRMS m/z 508.0673 (M+H calcd for C₂₂H₂₁BrF₂N₃O₄ requires 508.0678).

Example 556

6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylnicotinamide

Following the method of Example 554 (step 3) and substituting dimethylamine for the ethanolamine obtained the title compound as a white solid (75% yield). ¹H NMR (400 MHz, CDCl₃) δ 8.55 (d, J=1.62 Hz, 1H), 7.68 (dd, J=5.77, 2.15 Hz, 1H), 7.55 (app q, J=6.45 Hz, 1H), 7.37 (d, J=8.06 Hz, 1H), 6.93 (m, 1H), 6.84 (m, 1H), 6.02(s, 1H), 5.40 (s, 2H), 5.20 (s, 2H), 3.09 (s, 3H), 2.97 (s, 3H), 2.45 (s, 3H); LC/MS, t_r=2.45 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-HRMS m/z 492.0710 (M+H calcd for C₂₂H₂₁BrF₂N₃O₃ requires 492.0729).

Example 557

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(trifluoromethyl)phenyl]pyridin-2(1H)-one

Step 1: Preparation of 4-hydroxy-6-methyl-1-[2-(trifluoromethyl)phenyl]pyridin-2(1H)-one

4-hydroxy-6-methyl-2-pyrone (10 g, 79.3 mmol) was added into the 2-(trifluoromethyl) aniline (14 ml, 111.3 mmol) in 10 ml of 1,2-dichlorobenzene in a round bottom flask. The mixture was then placed in a pre-heated oil bath at 165 C. After 30 minute of heating, the mixture was cooled to room temperature and added 250 ml of saturated sodium bicarbonate solution. The mixture was stirred at room temperature for 15 minutes and transferred to a separatory funnel. Ethyl acetate (300 ml) was added into the separatory funnel and partitions the layers. The aqueous layer was obtained and the organic layer was added 200 ml of saturated sodium bicarbonate solution. The aqueous layer was obtained again and the combined aqueous solution was neutralized with HCl solution. Upon neutralization, white solid precipitated out of the solution. Filtered the solid, rinsed with water (100 ml×5) and dried over high vacuum oven to obtain the white solid (7.5 g, 35.5%). LC/MS, t_r=1.77 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 270 (M+H).

Step 2: Preparation of 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(trifluoromethyl)phenyl]pyridin-2(1H)-one

4-hydroxy-6-methyl-1-[2-(trifluoromethyl)phenyl]pyridin-2(1H)-one (from Step 1) (7.3 g, 27.1 mmol) was added into 3,4-difluorobenzyl bromide (5.5 g, 26.5 mmol) in 60 ml of dimethyl formamide. The mixture was cooled to 0 C and cesium carbonate (20 g, 61.3 mmol) was added into the mixture. After the addition, the mixture was warmed to room temperature and stirred for 4 hours. Water (500 ml) was added into the reaction mixture. Yellow solid came out of solution. Filtered and rinsed with water (200 ml×2) to obtain the yellow solid. Dissolved the solid in ethyl acetate (500 ml) and water (300 ml) and transfer to a separatory funnel and obtained the organic layer. The organic layer was washed again with water (200 ml) and dried over anhydrous magnesium sulfate. The organic solution was evaporated to dryness. ¹H NMR (400 MHz, CDCl₃) δ 7.82 (d, J=7.65 Hz, 1H), 7.7 (t, J=7.52 Hz, 1H), 7.58 (t, J=7.65 Hz, 1H), 7.42 (q, J=6.45 Hz, 1H), 7.27 (d, J=7.78 Hz, 2H), 6.89 (m, 2H), 5.95 (app d, J=2.42 Hz, 1H), 5.90 (app d, J=2.42 Hz, 1H), 5.01 (app d, J=2.94 Hz, 2H), 1.86 (s, 3H); LC/MS, t_r=2.74 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 396 (M+H).

Step 3: Preparation of the Title Compound

N-bromosuccinimide (0.24 g, 1.36 mmol) was added into 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(trifluoromethyl)phenyl]pyridin-2(1H)-one (0.54 g, 1.36 mmol) in 20 ml of dichloromethane. The mixture was stirred at room temperature for 2 hours. Saturated sodium bicarbonate solution (150 ml) was added into the reaction mixture and the combine solution was transferred to a separatory funnel. The product was extracted with ethyl acetate (250 ml). The ethyl acetate solution was dried over anhydrous magnesium sulfate and evaporated to dryness. ¹H NMR (400 MHz, CDCl₃) δ 7.82 (d, J=7.25 Hz, 1H), 7.7 (app t, J=7.66 Hz, 1H), 7.60 (m, 2H), 7.26 (s, 1H), 6.97 (m, 1H), 6.87 (m, 1H), 6.09 (s, 1H), 5.25 (app d, J=3.35 Hz, 2H), 1.94 (s, 3H); LC/MS, t_r=2.84 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-HRMS m/z 474.0113 (M+H calcd for C₂₀H₁₄BrF₅NO₂ requires 474.0123).

Example 558

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methyl-5-vinylpyridin-2(1H)-one

Step 1: To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one (1.00 g, 1.76 mmol) in anhydrous THF (12 mL) was added, sequentially, tributyl(vinyl)tin (1.21 g, 3.81 mmol) and tetrakis(triphenylphosphine)palladium (236 mg, 0.204 mmol) under an argon stream. The reaction vessel was then equipped with a reflux condenser and the reaction system purged with an argon flow. The resulting yellow solution was heated to 68° C. and stirred under a positive pressure of argon for 12.0 hours until complete disappearance of starting material by LCMS analysis. The reaction mixture was concentrated in vacuo and the resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a reddish solid. ¹H NMR (400 MHz, CDCl₃) δ 7.62 (app q, J=7.8 Hz, 1H), 7.45 (app tt, J=8.4, 6.2, 1H), 7.09 (app t, J=8.8 Hz, 2H), 6.90 (app t, J=8.0 Hz, 1H), 6.83 (app dt, J=6.8, 2.5 Hz, 1H), 6.51 (dd, J=17.7, 11.4 Hz, 1H), 5.53 (dd, J=11.4, 1.5 Hz, 1H), 5.41 (dd, J=17.8, 1.5 Hz, 1H), 5.09 (br s, 2H), 2.09 (s, 3H); LC/MS C-18 column, t_r=3.20 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 468 (M+H). ES-HRMS m/z 468.0210 (M+H calcd for C₂₁H₁₅BrF₄NO₂ requires 468.0217).

Example 560

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-(1,2-dihydroxyethyl)-6-methylpyridin-2(1H)-one

Step 1: To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methyl-5-vinylpyridin-2(1H)-one (0.970 g, 2.07 mmol) in water/acetone 1:3 (8.7 mL) was added, sequentially, osmium tetroxide (0.110 g, 0.433 mmol) and N-methyl morpholine oxide (1.32 g, 11.2 mmol). The resulting solution was stirred for one hour until complete consumption of starting material by LCMS analysis, and the reaction was concentrated in vacuo. The resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a solid. ¹H NMR (400 MHz, CDCl₃) δ 7.59 (app q, J=8.2 Hz, 1H), 7.45 (ddd, J=14.7, 8.5, 6.8 Hz, 1H), 7.08 (app t, J=8.5 Hz, 2H), 6.94 (app t, J=8.2 Hz, 1H), 6.88 (app t, J=8.5 Hz, 1H), 5.31 (AB-q, J=10.6 Hz, Δ=38.3 Hz, 2H), 5.07 (dd, J=9.1, 3.8 Hz, 1H), 3.83 (t, J=10.8 Hz, 1H), 3.60 (dd, J=11.4, 3.9 Hz, 1H), 2.94 (br s, 1H), 2.16 (s, 3H); LC/MS C-18 column, t_r=2.26 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 502 (M+H). ES-HRMS m/z 502.0276 (M+H calcd for C₂₁H₁₇BrF₄NO₄ requires 502.0272).

Example 561

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-(hydroxymethyl)-6-methylpyridin-2(1H)-one

Step 1: To a −20° C. solution of 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde (0.659 g, 1.40 mmol) in methanol (10 mL) was added, portionwise, solid sodium borohyride (3.6 g, 96 mmol) over one hour until complete consumption of starting material by LCMS analysis. Next, the reaction mixture was diluted with 500 mL of ethyl acetate and washed with 3×200 mL of water. The resulting organic extract was Na₂SO₄ dried, filtered, and concentrated in vacuo to approximately 100 mL volume. The resulting liquid was diluted with hexanes (100 mL) to furnish an amorphous solid that was collected and dried at 1 mm Hg vacuum to furnish (620 mg, 94%) of the desired product. ¹H NMR (400 MHz, d₄-MeOH) δ 7.70 (app q, J=8.3 Hz, 1H), 7.62 (app tt, J=10.4, 6.3 Hz, 1H), 7.25 (app t, J=8.6 Hz, 2H), 7.03 (app t, J=8.6 Hz, 1H), 6.88 (app t, J=8.5 Hz, 1H), 5.31 (s, 2H), 4.58 (s, 2H), 2.17 (s, 3H); LC/MS C-18 column, t_r=2.49 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 472 (M+H). ES-HRMS m/z 472.0152 (M+H calcd for C₂₀H₁₅BrF₄NO₃ requires 472.0166).

Example 562

4-(benzyloxy)-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-(benzyloxy)-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one.

To a briskly stirred room temperature solution of 1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (1.43 g, 6.03 mmol) in dimethylformamide (4.6 mL) was added sequentially K₂CO₃ (2.01 g, 14.5 mmol) and benzyl bromide (2.40 mL, 20.2 mmol). The resulting suspension was stirred for 6.5 hours until complete consumption of starting material by LCMS analysis. The reaction was then diluted with ethyl acetate (200 mL) and brine washed (3×200 mL). The resulting organic extract was Na₂SO₄ dried, filtered, and concentrated in vacuo to approximately 100 mL volume. The resulting mother liquor rapidly precipitated and furnished an amorphous solid that was collected and dried at 1 mm Hg vacuum to provide a solid (1.62 g, 82%). ¹H NMR (300 MHz, d₄-MeOH) δ 7.62 (app tt, J=8.6, 6.4 Hz, 1H), 7.52-7.32 (m, 4H), 7.30-7.12 (m, 3H), 6.27 (d, J=1.6 Hz, 1H), 6.04 (d, J=2.6 Hz, 1H), 5.18 (s, 2H), 2.06 (s, 3H). LC/MS C-18 column, t_r=2.51 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 328 (M+H). ES-HRMS m/z 328.1179 (M+H calcd for C₁₉H₁₆F₂NO₂ requires 328.1144).

Step 2: To a room temperature solution of 4-(benzyloxy)-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one (1.52 g, 4.64 mmol) in methylene chloride (15 mL) was added solid N-bromosuccinimide (2.01 g, 11.3 mmol) and the resulting reddish solution was stirred for 4.0 hours. At this time the reaction was diluted with ethyl acetate (400 mL) and washed with sodium sulfite (5% aqueous solution, 100 mL) and brine (3×200 mL). The resulting organic extracts were Na₂SO₄ dried, filtered, and concentrated in vacuo to approximately 60 mL volume. The resulting mother liquor rapidly precipitated and furnished an amorphous solid that was collected and dried at 1 mm Hg vacuum to provide a solid 4-(benzyloxy)-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one (1.70 g, 91%). ¹H NMR (300 MHz, d₄-MeOH) δ 7.64 (app tt, J=8.6, 6.4 Hz, 1H), 7.57 (br d, J=7.1 Hz, 1H), 7.50-7.34 (m, 4H), 7.27 (app t, J=8.0 Hz, 1H), 7.26-7.21 (m, 1H), 6.66 (s, 1H), 5.40 (s, 2H), 2.12 (s, 3H); LC/MS C-18 column, t_r=2.63 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 406 (M+H). ES-HRMS m/z 406.0228 (M+H calcd for C₁₉H₁₅BrF₂NO₂ requires 406.0249).

Example 563

5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridin-3-yl]methyl Carbamate

Step 1: To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-(hydroxymethyl)-6-methylpyridin-2(1H)-one (76.2 mg, 0.161 mmol) in methylene chloride (0.4 mL) was added a solution of trichloroacetyl isocyanate (toluene, 0.60 M, 0.5 mL, 0.30 mmol). The resulting solution was stirred for one hour until complete consumption of starting material by LCMS analysis. The reaction mixture was then directly applied to Al₂O₃ (0.5 g of Broeckman-activity type I) and the slurry was matured for three hours. At this time, the Al₂O₃ plug was flushed with ethyl acetate/methanol (95:5) and the resulting mother liquor was concentrated to a residue that was subjected to SiO₂ chromatography using ethyl acetate/hexanes (1:1) to furnish a white solid (71.0 mg, 85%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.71-7.59 (m, 2H), 7.26 (app t, J=8.5 Hz, 2H), 7.02 (app t, J=9.2 Hz, 2H), 5.32 (s, 2H), 5.02 (s, 2H), 2.15 (s, 3H); LC/MS C-18 column, t_r=2.35 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 515 (M+H). ES-HRMS m/z 515.0188 (M+H calcd for C₂₁H₁₆BrF₄N₂O₄ requires 515.0224).

Example 564

5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde

Step 1: To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-(1,2-dihydroxyethyl)-6-methylpyridin-2(1H)-one (550 mg, 1.10 mmol) in toluene (10.0 mL) was added lead(IV) acetate (810 mg, 1.82 mmol). The resulting dark brown solution was stirred for two hours until complete consumption of starting material by LCMS analysis. The reaction mixture was then diluted with ethyl acetate (400 mL), water washed (3×100 mL), and brine washed (3×300 mL). The resulting organic extract was separated, Na₂SO₄ dried, and concentrated. The resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (1:1) to furnish a light yellow solid (321 mg, 62%). ¹H NMR (400 MHz, CDCl₃) δ 10.08 (s, 1H), 7.56-7.48 (m, 2H), 7.12 (app t, J=7.3 Hz, 2H), 6.94 (app t, J=8.5 Hz, 1H), 6.88 (app t, J=8.7 Hz, 1H), 5.33 (s, 2H), 2.45 (s, 3H); LC/MS C-18 column, t_r=2.94 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 470 (M+H). ES-HRMS m/z 469.9996 (M+H calcd for C₂₀H₁₃BrF₄NO₃ requires 470.0009).

Example 565

5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde Oxime

Step 1: To a room temperature solution of 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde (316.5 mg, 0.673 mmol) in methanol (10.0 mL) was added solid NH₂OH.H₂O (300.0 mg, 4.32 mmol) and sodium acetate (480.0 mg, 5.85 mmol). The resulting suspension was stirred for 1.5 hours until complete consumption of starting material by LCMS analysis. The reaction mixture was then concentrated in vacuo and the resulting residue was diluted with methylene chloride (300 mL) and water washed (2×100 mL). The resulting organic extract was separated, Na₂SO₄ dried, and concentrated to furnish a light yellow solid (390 mg, 99%). ¹H NMR (400 MHz, d₄-MeOH with CDCl₃) δ 8.06 (s, 1H), 7.51-7.40 (m, 2H), 7.06 (app dd, J=8.6, 7.4 Hz, 2H), 6.88 (app dt, J=8.3, 2.4 Hz, 1H), 6.83 (app dt, J=9.2, 2.4 Hz, 1H), 5.13 (s, 2H), 2.76 (s, 3H); LC/MS C-18 column, t_r=2.61 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 485 (M+H). ES-HRMS m/z 485.0093 (M+H calcd for C₂₀H₁₄BrF₄N₂O₃ requires 485.0118).

Example 566

5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbonitrile

Step 1: To a room temperature solution of 5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-2-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde oxime (340.0 mg, 0.701 mmol) in methylene chloride (8.0 mL) was added solid 1,1′ carbonyl diimidazole (290.0 mg, 1.79 mmol) and sodium acetate (480.0 mg, 5.85 mmol). The resulting solution was stirred for 1.5 hours until complete consumption of starting material by LCMS analysis. The reaction mixture was then concentrated in vacuo and the resulting residue was directly applied to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a white solid (262 mg, 90%). ¹H NMR (400 MHz, CDCl₃) δ 7.61 (app q, J=7.4 Hz, 1H), 7.52 (app tt, J=8.4, 6.3 Hz, 1H), 7.14 (app dd, J=8.6, 7.4 Hz, 2H), 6.94 (app dt, J=8.5, 2.5 Hz, 1H), 6.88 (app dt, J=8.5, 2.4 Hz, 1H), 5.43 (s, 2H), 2.32 (s, 3H); LC/MS C-18 column, t_r=2.95 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). IR (neat) 3111, 3067, 3032, 2914, 2840, 2215 (nitrile stretch), 1678, 1587, 1470 cm⁻¹; ES-MS m/z 467 (M+H). ES-HRMS m/z 467.0037 (M+H calcd for C₂₀H₁₂BrF₄N₂O₂ requires 467.0013).

Example 567

4-(benzyloxy)-3-bromo-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one

Step 1: A solution of 4-(benzyloxy)-3-bromo-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one (1.42 g, 3.50 mmol) in 1,2 dichloroethane (18 mL) was treated with solid N-iodosuccinimide (1.59 g, 7.06 mmol) and dichloroacetic acid (0.260 g, 2.01 mmol). The resulting solution was stirred and heated to 50° C. for 2.5 hours until complete consumption of starting material by LCMS. At this time the reaction was diluted with ethyl acetate (400 mL) and washed with sodium sulfite (5% aqueous solution, 100 mL) and brine (3×200 mL). The resulting organic extracts were Na₂SO₄ dried, filtered, and concentrated in vacuo to approximately 30 mL volume. The resulting mother liquor rapidly precipitated and furnished an amorphous solid that was collected and dried at 1 mm Hg vacuum to provide a solid (1.49 g, 82%). ¹H NMR (400 MHz, CDCl₃) δ 7.62 (app d, J=6.8 Hz, 2H), 7.51-7.38 (m, 4H), 7.09 (app t, J=8.0 Hz, 2H), 5.20 (s, 2H), 2.39 (s, 3H); LC/MS C-18 column, t_r=3.28 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 532 (M+H). ES-HRMS m/z 531.9196 (M+H calcd for C₁₉H₁₄BrF₂INO₂ requires 531.9215).

Example 568

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methyl-5-oxiran-2-ylpyridin-2(1H)-one

Step 1: A sample of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methyl-5-vinylpyridin-2(1H)-one (10.0 mg, 0.0214 mmol) was treated with a solution of dimethyl dioxirane in acetone (approx. 0.1 M, 5 mL, 0.5 mmol). The reaction vessel was capped and sealed, and the resulting solution was stirred 6.0 hours. At this time the reaction was concentrated in vacuo and the resulting residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (4:6) to furnish a semi-solid (5.0 mg, 48%). ¹H NMR (400 MHz, CDCl₃) δ 7.57 (app q, J=7.4 Hz, 1H), 7.46 (app tt, J=8.5, 6.2, 1H), 7.11 (app t, J=8.0 Hz, 2H), 6.94 (app t, J=8.2 Hz, 1H), 6.83 (app t, J=9.2 Hz, 1H), 5.31 (AB-q, J=10.9 Hz, Δ=29.0 Hz, 2H), 3.63 (app t, J=3.5 Hz, 1H), 3.03 (dd, J=9.4, 5.0, 1H), 2.85 (dd, J=5.2, 2.7, 1H), 2.14 (s, 3H); LC/MS C-18 column, t_r=2.26 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 484 (M+H) and 502 (M+H₃O). ES-HRMS m/z 502.0273 (M+H₃O calcd for C₂₁H₁₇BrF₄NO₄ requires 502.0272).

Example 569

4-(benzylamino)-3-bromo-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one

Step 1: A slurry of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one (80.0 mg, 0.141 mmol) and benzyl amine (300 mg, 2.80 mmol) was heated to 63° C. and stirred for 1.0 hours until complete disappearance of starting material by LCMS analysis. The reaction mixture was then diluted with ethyl acetate (300 mL) and brine washed (3 X 200 mL). The resulting organic extracts were Na₂SO₄ dried, filtered, and concentrated in vacuo to a residue that was then subjected to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a brown solid (60.0 mg, 81%). ¹H NMR (400 MHz, CDCl₃) δ 7.43-7.22 (m, 6H), 7.04 (app t, J=8.4 Hz, 2H), 5.02 (br t, J=1.6 Hz, 1H), 4.86 (d, J=5.5 Hz, 2H), 2.37 (s, 3H); LC/MS C-18 column, t_r=3.02 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 531 (M+H). ES-HRMS m/z 530.9344 (M+H calcd for C₁₉H₁₅BrF₂IN₂O requires 530.9375).

Example 570

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methyl-5-[(E)-2-phenylethenyl]pyridin-2(1H)-one

Step 1: To an anhydrous −78° C. solution of β-bromostyrene (1.80 g, 10.0 mmol) in ether (18 mL) was added sequentially a solution of zinc chloride (10.0 mL, 1.0 M ether, 10.0 mmol) over 1.0 minute and a solution of tert-butyl lithium (15.0 mL, 1.6 M pentanes, 24.0 mmol) over 8.0 minutes. The resulting solution became cloudy and the reaction mixture was allowed to warm to room temperature on its own accord (over 30 minutes). After an additional 1.0 hour, the suspension was transferred by syringe directly to a separate vessel containing a solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one (1.50 g, 2.64 mmol) and tetrakis(tripheylphosphine)palladium (294 mg, 0.254 mmol) in anhydrous THF (4 mL). This resulting suspension was heated to 55° C. for 40 minutes and cooled to room temperature, whereby it was stirred under a positive pressure of argon for an additional 4.0 hours until complete disappearance of starting material by LCMS analysis. The reaction suspension was subsequently treated with NaHCO₃ and brine (100 and 200 mL, respectively). The resulting emulsion was extracted with ethyl acetate (3×300 mL) and the organic extracts were Na₂SO₄ dried, filtered, and concentrated in vacuo to a residue that was then subjected to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a reddish solid (1.25 g, 86%). ¹H NMR (400 MHz, CDCl₃) δ 7.51-7.39 (m, 2H), 7.38-7.24 (m, 5H), 7.10 (app t, J=8.5 Hz, 2H), 6.84 (d, J=17.2 Hz, 1H), 6.82-6.75 (m, 1H), 6.74-6.68 (m, 1H), 6.69 (d, J=17.2, 1H), 5.11 (br s, 2H), 2.15 (s, 3H); LC/MS C-18 column, t_r=3.74 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 544 (M+H). ES-HRMS m/z 544.0565 (M+H calcd for C₂₇H₁₉BrF₄NO₂ requires 544.0530).

Example 574

4-(allylamino)-3-bromo-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one

Step 1: A slurry of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one (1.40 g, 2.46 mmol) and allyl amine (1.98 mg, 34.6 mmol) was heated to 50° C. and stirred for 1.0 hours until complete disappearance of starting material by LCMS analysis. The reaction mixture was then concentrated in vacuo (1.0 mm Hg) for 2 days at 50° C. to furnish a brown solid (1.18 g, 99%). ¹H NMR (300 MHz, CDCl₃) δ 7.43 (app tt, J=8.4, 6.2, 1H), 7.09 (app t, J=8.4 Hz, 2H), 6.02 (app dq, J=11.0, 6.2 Hz, 1H), 5.39 (dd, J=16.9, 1.8 Hz, 1H), 5.30 (dd, J=11.0, 1.8 Hz, 1H), 4.84 (br s, 1H), 4.35 (br s, 2H), 2.42 (s, 3H); LC/MS C-18 column, t_r=2.71 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 481 (M+H). ES-HRMS m/z 480.9261 (M+H calcd for C₁₅H₁₃BrF₂IN₂O requires 480.9219).

Example 575

4-(allylamino)-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one

Step 1: A solution of 4-(allylamino)-3-bromo-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one (1.00 g, 2.07 mmol) and tetrakis(tripheylphosphine)palladium (420 mg, 0.363 mmol) in anhydrous THF (10 mL) under an argon stream was heated to 64° C. and stirred for 12 hours until complete disappearance of starting material by LCMS analysis. The reaction suspension was subsequently treated with brine (600 mL). The resulting emulsion was extracted with ethyl acetate (3×400 mL) and the organic extracts were anhy. Na₂SO₄ dried, filtered, and concentrated in vacuo to a residue that was then subjected to SiO₂ chromatography with ethyl acetate/hexanes (gradient 3:7) to furnish a solid (376 mg, 45%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.55 (app tt, J=8.7, 6.3, 1H), 7.18 (app t, J=7.6 Hz, 2H), 5.89 (app ddd, J=15.4, 10.3, 5.1 Hz, 1H), 5.01 (app d, J=17.0, Hz, 1H), 5.50 (s, 1H), 5.22 (app d, J=11.0 Hz, 1H), 4.35 (app d, J=5.0 Hz, 2H), 2.36 (s, 3H); LC/MS C-18 column, t_r=2.33 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 403 (M+H). ES-HRMS m/z 403.0133 (M+H calcd for C₁₅H₁₄F₂IN₂O requires 403.0113).

Example 576

4-(allylamino)-1-(2,6-difluorophenyl)-5-iodo-6-methylpyridin-2(1H)-one

Step 1: A solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one (197 mg, 0.445 mmol) and allyl amine (1.32 mg, 23.1 mmol) in THF (6.0 mL) was heated to 68° C. and stirred for 74.0 hours. The reaction mixture was then concentrated in vacuo (30 mm Hg) to furnish a residue that was subjected to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a solid (36.0 mg, 23%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.55 (app tt, J=8.5, 6.5, 1H), 7.18 (app t, J=8.5 Hz, 2H), 6.14 (s, 1H), 5.91 (app dq, J=11.5, 6.4 Hz, 1H), 5.23 (dd, J=17.0, 1.5 Hz, 1H), 5.19 (dd, J=11.0, 1.6 Hz, 1H), 4.00 (app d, J=4.7 Hz, 2H), 1.98 (s, 3H); LC/MS C-18 column, t_r=2.24 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 355 (M+H). ES-HRMS m/z 355.0257 (M+H calcd for C₁₅H₁₄F₂BrF₂N₂O requires 355.0252).

Example 577

Ethyl 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,2′-bipyridine-5′-carboxylate

Step 1: To a room temperature suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (500.0 mg, 1.51 mmol) and Cs₂CO₃ (1.50 g, 4.60 mmol) in 1-methyl-2-pyrrolidinone (3.0 mL) was added ethyl 6-chloronicotinate (900 mg, 4.85 mmol). The resulting suspension was stirred and heated to 106° C. for 36 hours until complete consumption of starting material by LCMS analysis. The reaction mixture was then diluted with ethyl acetate (400 mL), water washed (3×200 mL). The resulting organic extract was separated, Na₂SO₄ dried, and concentrated. The resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a solid. ¹H NMR (400 MHz, d₄-MeOH) δ 8.68 (app d, J=2.5 Hz, 1H), 8.39 (dd, J=8.7, 2.3 Hz, 1H), 7.62 (app q, J=8.2 Hz, 1H), 7.15 (d, J=8.6 Hz, 1H), 7.08 (s, 1H), 7.08-6.99 (m, 2H), 5.31 (s, 2H), 4.37 (q, J=7.1 Hz, 2H), 2.43 (s, 3H), 1.37 (t, J=7.1 Hz, 3H); LC/MS C-18 column, t_r=3.44 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 479 (M+H). ES-HRMS m/z 479.0401 (M+H calcd for C₂₁H₁₈BrF₂N₂O₄ requires 479.0431).

Example 578

3-bromo-4-[(2,4-difluorobenzyl)oxy]-5′-(1-hydroxy-1-methylethyl)-6-methyl-2H-1,2′-bipyridin-2-one

Step 1: To a 0° C. solution of methyl magnesium bromide (3.0 M, 3.5 mL, 10.5 mmol) was added dropwise over 15 minutes a solution of ethyl 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,2′-bipyridine-5′-carboxylate (500.0 mg, 1.05 mmol) in THF (4.0 mL). The internal temperature of the reaction was never allowed to exceed 0° C. The resulting solution was maintained for 30 minutes until complete consumption of starting material by LCMS analysis. Next, a solution of ammonium chloride (saturated aqueous, 160 mL) was added. The reaction mixture was extracted with ethyl acetate (3×100 mL) and the resulting organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo to a residue that was subjected to SiO₂ chromatography with ethyl acetate/hexanes (gradient 3:7 to 6:4) to furnish a solid (386 mg, 79%). ¹H NMR (400 MHz, d₄-MeOH) δ 8.23 (app d, J=2.8 Hz, 1H), 7.97 (dd, J=8.6, 2.3 Hz, 1H), 7.61 (app q, J=8.2 Hz, 1H), 7.06-7.00 (m, 3H), 7.00 (s, 1H), 5.30 (s, 2H), 2.38 (s, 3H), 1.54 (s, 6H); LC/MS C-18 column, t_r=2.75 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 465 (M+H). ES-HRMS m/z 465.0615 (M+H calcd for C₂₁H₂₀BrF₂N₂O₃ requires 465.0620). IR (neat) 3366, 3030, 2974, 1600, 1507, 1362, 1232 cm⁻¹. ¹³C NMR (400 MHz, d₄-MeOH, visible peaks with carbon fluorine coupling present) δ 164.4, 160.7, 158.9, 157.6, 143.6, 141.6, 137.5, 131.61, 131.56, 131.51, 131.46, 119.29, 119.25, 119.15, 119.11, 112.23, 111.55, 111.52, 111.33, 111.29, 106.0, 103.9, 103.7, 103.4, 96.8, 70.3, 64.9, 64.8, 30.5, 22.6.

Example 579

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2-furylmethyl)-6-methylpyridin-2(1H)-one

Step 1: Preparation of the title compound. To a room temperature suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (330.0 mg, 1.00 mmol)) and NaH (48.0 mg, 2.0 mmol) in THF (3.0 mL) was added 2—(Chloromethyl)furan (461 mg, 3.97 mmol). The resulting suspension was stirred and heated to 68° C. for 9 hours until complete consumption of starting material by LCMS analysis. The reaction mixture was then diluted with ethyl acetate (400 mL), water washed (3×200 mL). The resulting organic extract was separated, Na₂SO₄ dried, and concentrated. The resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (4:6) to furnish a solid. ¹H NMR (300 MHz, d₄-MeOH) δ 7.62 (app q, J=8.4 Hz, 1H), 7.46 (s, 1H), 7.06 (app t, J=8.7 Hz, 2H), 6.51 (s, 1H), 6.41-6.37 (m, 2H), 5.37 (s, 2H), 5.32 (s, 2H), 2.61 (s, 3H); LC/MS C-18 column, t_r=2.63 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 410 (M+H). ES-HRMS m/z 410.0177 (M+H calcd for C₁₈H₁₅BrF₂NO₃ requires 410.0198).

Example 580

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(thien-2-ylmethyl)pyridin-2(1H)-one

Step 1: To a room temperature suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (330.0 mg, 1.00 mmol) and NaH (48.0 mg, 2.0 mmol) in THF (3.0 mL) was added 2—(Chloromethyl)thiophene (461 mg, 3.97 mmol). The resulting suspension was stirred and heated to 68° C. for 12 hours until complete consumption of starting material by LCMS analysis. The reaction mixture was then diluted with ethyl acetate (400 mL), water washed (3×200 mL). The resulting organic extract was separated, Na₂SO₄ dried, and concentrated. The resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (4:6) to furnish a solid. ¹H NMR (400 MHz, d₄-MeOH) δ 7.58 (app q, J=8.2 Hz, 1H), 7.30 (app dd, J=5.1, 1.2 Hz, 1H), 7.05 (d, J=2.6 Hz, 1H), 7.01 (app t, J=8.1 Hz, 2H), 6.93 (dd, J=5.1, 3.4 Hz, 1H), 6.43 (s, 1H), 5.49 (s, 2H), 5.25 (s, 2H), 2.51 (s, 3H); LC/MS C-18 column, t_r=2.74 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 426 (M+H). ES-HRMS m/z 425.9936 (M+H calcd for C₁₈H₁₅BrF₂NO₂S requires 425.9969).

Example 581

3-bromo-1-(2,6-difluorophenyl)-4-(2-furylmethoxy)-6-methylpyridin-2(1H)-one

Step 1: To a suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one (250 mg, 0.445 mmol) and furfuryl alcohol (198 mg, 2.0 mmol) in THF (2.5 mL) was added solid NaH (46.0 mg, 1.92 mmol). Following the evolution of gas, the resulting suspension laws heated to 60° C. and stirred for 3.5 hours until complete consumption of starting material by LCMS analysis. The reaction mixture was then diluted with ammonium chloride (saturated aqueous, 100 mL) and extracted with ethyl acetate (3×100 mL). The resulting organic extracts were separated, Na₂SO₄ dried, and concentrated to provide a residue that was subjected to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a solid (110.0 mg, 49%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.63 (app tt, J=8.5, 6.2, 1H), 7.62-7.61 (m, 1H), 7.28 (app t, J=8.5 Hz, 2H), 6.77 (s, 1H), 6.68 (d, J=4.1 Hz, 1H), 6.51(dd, J=4.2, 3.9 Hz, 1H), 5.34 (s, 2H), 2.15 (s, 3H); LC/MS C-18 column, t, =2.43 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 396 (M+H). ES-HRMS m/z 396.0044 (M+H calcd for C₁₇H₁₃BrF₂NO₃ requires 396.0041).

Example 582

3-bromo-1-[2-fluoro-6-(3-furylmethoxy)phenyl]-4-(3-furylmethoxy)-6-methylpyridin-2(1H)-one

By following the method of preparation of 3-bromo-1-(2,6-difluorophenyl)-4-(2-furylmethoxy)-6-methylpyridin-2(1H)-one (Example 581) and substituting 3-furylmethanol for furfuryl alcohol, the title compound was prepared in 55% chemical yield. ¹H NMR (400 MHz, d₄-MeOH) δ 7.64 (s, 1H), 7.55-7.42 (m, 3H), 7.40 (app t, J=1.4 Hz, 1H), 7.12 (d, J=9.0 Hz, 1H), 6.92 (app t, J=8.4 Hz, 1H), 6.58 (s, 2H), 6.34 (br s, 1H), 5.21 (s, 2H), 5.03 (AB-q, J=14.0 Hz, Δ=58.0 Hz, 2H), 1.99 (s, 3H); LC/MS C-18 column, t_r=2.67 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 474 (M+H). ES-HRMS m/z 474.0346 (M+H calcd for C₂₂H₁₈BrFNO₅ requires 474.0347).

Example 583

3-bromo-1-[2-fluoro-6-(thien-3-ylmethoxy)phenyl]-6-methyl-4-(thien-3-ylmethoxy)pyridin-2(1H)-one

By following the method of preparation of 3-bromo-1-(2,6-difluorophenyl)-4-(2-furylmethoxy)-6-methylpyridin-2(1H)-one Example 581 and substituting thien-3-ylmethanol for furfuryl alcohol, the title compound was prepared in 38% chemical yield. ¹H NMR (400 MHz, d₄-MeOH) δ 7.50-7.42 (m, 3H), 7.33 (dd, J=5.0, 3.0 Hz, 1H), 7.26 (br d, J=2.0 Hz, 1H), 7.19 (dd, J=5.0, 1.2 Hz, 1H), 7.09 (d, J=8.6 Hz, 1H), 6.98 (dd, J=14.9, 1.3 Hz, 1H), 6.93 (dt, J=8.7, 1.0 Hz, 1H), 6.53 (br s, 1H), 5.33 (s, 2H), 5.14 (AB-q, J=12.1 Hz, Δ=50.0 Hz, 2H), 1.97 (s, 3H); LC/MS C-18 column, t_r=2.93 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 506 (M+H). ES-HRMS m/z 505.9881 (M+H calcd for C₂₂H₁₈BrFNO₃S₂ requires 505.9890).

Example 584

Methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzoate

Step 1: Preparation of 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-(methoxycarbonyl)benzoic Acid

4-Hydroxy-6-methyl-2-pyrone (75.0 g, 595 mmol) and 3-amino-4-(methoxycarbonyl)benzoic acid (40.0 g, 0.205 mmol) were suspended in 56 ml of 1,2-dichlorobenzene in a 500 ml, 3-necked, round bottom flask equipped with a J-Kem temperature controller probe, a Dean-Stark trap, and a heating mantle. The reaction was heated to 180° C. over a period of 26 minutes during which time all solids dissolved. Upon reaching an internal temperature of 180° C., the reaction was allowed to maintain this temperature for an additional 25.0 minutes during which time the evolution of water from the reaction mixture was evident. Next, the heating apparatus was removed and the reaction was allowed to cool on its own accord to about 100° C. The reaction was then diluted with 160 ml of toluene and stirred. After about 10 minutes, the reaction reached room temperature and a gummy solid had formed. The precipitate was filtered, washed with EtOAc (400 mL) and water (200 mL, 55° C.), and dried in vacuo to give a tan solid (30.5 g, 49%). ¹H NMR (400 MHz, d₄-MeOH) δ 8.20-8.09 (m, 2H), 7.84 (s, 1H), 6.08 (app d, J=1.0 Hz, 1H), 5.76 (app d, J=2.3 Hz, 1H), 3.76 (s, 3H), 1.91 (s, 3H). LC/MS, C-18 column, t_r=1.96 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 304 (M+H). ES-HRMS m/z 304.0803 (M+H calcd for C₁₅H₁₄NO₆ requires 304.0816).

Step 2: Preparation of Methyl 2-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-[(methylamino)carbonyl]benzoate

To a solution of 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-(methoxycarbonyl)benzoic acid (from Step 1) (1.00 g, 3.30 mmol) in dimethylformamide (10 mL) and THF (10 mL) was added cyclohexylcarbodiimide-derivatized silica gel (a product of Silicycle chemical division Quebec, Canada) with a loading of 0.60 mmol/g (15.2 g, 9.73 mmol). After stirring for 30 minutes, a solution of methylamine (2.0 M, THF, 2.9 mL, 5.8 mmol) was added followed by the addition of 1-hydroxy-benzotriazole (20.0 mg, 0.15 mmol). The reaction suspension was allowed to stir for 24 hours until the complete disappearance of starting material by LCMS analysis. The silica suspension was filtered and washed with 300 mL ethyl acetate/methanol (9:1) and 300 mL ethyl acetate/methanol (1:1). The resulting mother liquor was concentrated to furnish a brown semi-solid (898 mg, 86%). ¹H NMR (300 MHz, d₄-MeOH) δ 8.22 (d, J=8.0 Hz, 1H), 8.04 (dd, J=8.3, 1.9 Hz, 1H), 7.73 (d, J=1.6 Hz, 1H), 6.13 (d, J=1.5, Hz, 1H), 5.80 (d, J=2.2 Hz, 1H), 3.80 (s, 3H), 3.03 (s, 3H), 1.97 (s, 3H). LC/MS, C-18 column, t_r=1.31 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 317 (M+H). ES-HRMS m/z 317.1142 (M+H calcd for C₁₆H₁₇N₂O₅ requires 317.1132).

Step 3: Preparation of Methyl 2-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-[(methylamino)carbonyl]benzoate

To a room temperature suspension of methyl 2-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-[(methylamino)carbonyl]benzoate (from Step 2) (406.0 mg, 1.28 mmol) in CH₂Cl₂ (8 mL) was added solid N-bromosuccinimide (251 mg, 1.41 mmol) and stirred for 10 minutes until complete consumption of starting material by LCMS analysis. The reaction was next diluted with CH₂Cl₂ (5 mL), ethyl acetate (5 mL), and hexanes (1 mL). After approximately 30 minutes the resulting white precipitate was filtered and washed with ethyl acetate (5 mL) to furnish a solid (298 mg, 62%). ¹H NMR (400 MHz, d₄-MeOH) δ 8.20 (d, J=8.2 Hz, 1H), 8.01 (d, J=8.1 Hz, 1H), 7.69 (s, 1H), 6.18 (s 1H), 3.75 (s, 3H), 2.91 (s, 3H), 1.91 (s, 3H); LC/MS, t_r=1.27 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 395 (M+H). ES-HRMS m/z 395.0237 (M+H calcd for C₁₆H₁₆BrN₂O₅ requires 395.0237).

Step 4: Preparation of the Title Compound

To a solution of methyl 2-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-[(methylamino)carbonyl]benzoate (from Step 3) (241 mg, 0.610 mmol) in dimethylformamide (0.5 mL) was added sequentially K₂CO₃ (240 mg, 1.73 mmol) and 2,4 difluorobenzyl bromide (0.085 mL, 0.66 mmol). The resulting suspension was stirred for 6.5 hours until complete consumption of starting material by LCMS analysis. The reaction was then diluted with ethyl acetate (200 mL) and brine washed (3×200 mL). The resulting organic extract was Na₂SO₄ dried, filtered, and concentrated in vacuo to approximately 5 mL volume. The resulting mother liquor rapidly precipitated and furnished an amorphous solid that was collected. ¹H NMR (400 MHz, d₄-MeOH) 68.22 (d, J=8.2 Hz, 1H), 8.03 (dd, J=8.2, 1.7 Hz, 1H), 7.71 (d, J=1.8 Hz, 1H), 7.67 (app q, J=8.3 Hz, 1H), 7.05 (app t, J=8.6 Hz, 2H), 6.64 (s, 1H), 5.37 (s, 2H), 3.74 (s, 3H), 2.90 (s, 3H), 2.01 (s, 3H). LC/MS C-18 column, t_r=2.87 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 521 (M+H). ES-HRMS m/z 521.0491 (M+H calcd for C₂₃H₂₀BrF₂N₂O₅ requires 521.0518).

Example 585

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-(1-hydroxy-1-methylethyl)-N-methylbenzamide

Step 1: To a −10° C. solution of methyl magnesium bromide (3.0 M, 0.60 mL, 1.8 mmol) was added dropwise over 10 minutes a solution of methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzoate (85.0 mg, 0.163 mmol) in THF (1.0 mL). The internal temperature of the reaction was never allowed to exceed 0° C. The resulting solution was maintained for 10 minutes. Next, a solution of ammonium chloride (saturated aqueous, 100 mL) was added. The reaction mixture was removed from the bath and resulting emulsion was extracted with ethyl acetate (3×100 mL) and the resulting organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo to a residue that was subjected to SiO₂ chromatography with ethyl acetate/hexanes (gradient 3:7 to 6:4) to furnish a solid (16 mg, 19%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.89 (d, J=8.5 Hz, 1H), 7.78 (d, J=8.4 Hz, 1H), 7.61 (app q, J=8.2 Hz, 1H), 7.41 (s, 1H), 7.03-6.99 (m, 2H), 6.57 (s, 1H), 5.30 (s, 2H), 2.83 (s, 3H), 2.05 (s, 3H), 1.51 (s, 3H), 1.39 (s, 3H); LC/MS C-18 column, t_r=2.28 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 521 (M+H). ES-HRMS m/z 521.0860 (M+H calcd for C₂₄H₂₄BrF₂N₂O₄ requires 521.0882).

Example 586

3-bromo-1-[2-fluoro-6-(thien-3-ylmethoxy)phenyl]-6-methyl-4-(thien-3-ylmethoxy)pyridin-2(1H)-one

By following the method of preparation of 3-bromo-1-(2,6-difluorophenyl)-4-(2-furylmethoxy)-6-methylpyridin-2(1H)-one Example 581 and substituting 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide for 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one, the title compound was prepared in 76% chemical yield. ¹H NMR (400 MHz, d₄-MeOH) δ 7.83 (d, J=8.1 Hz, 2H), 7.54 (app d, J=1.1 Hz, 1H), 7.19 (d, J=8.1 Hz, 2H), 6.57 (d, J=3.2 Hz, 1H), 6.53 (s, 1H), 6.43 (dd, J=3.1, 1.8 Hz, 1H), 5.45 (br s, 2H), 5.22 (s, 2H), 2.34 (s, 3H); LC/MS C-18 column, t_r=1.98 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 417 (M+H). ES-HRMS m/z 417.0469 (M+H calcd for C₁₉H₁₈BrN₂O₄ requires 417.0444).

Example 587

(−)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

Example 489 (1.78 g, 4.36 mmol) were separated using a Chiral Technologies Chiralpak AD column (21 mm×250 mm, 20 μm) eluting with 100% ethanol (isocratic, 20 ml/min), loading 10 mg per injection. Fractions of the early-eluting atropisomer were pooled and concentrated in vacuo to the title compound (718 mg, 80%). Analytical chiral LC (Chiralpak AD, 4.6 mm×50 mm, 10 μm particle size, 0.5 ml/min ethanol) Retention time: 1.70 min, ee 94%. [α_D=−23.8° (5 mg/ml DMSO, 22° C.). ¹H NMR (400 MHz, DMSO-d₆) δ 8.42 (br qr, J=4.51 Hz, 1H), 7.82 (dd, J=7.92, 1.70 Hz, 1H), 7.68 (dt, J=8.24, 6.58 Hz, 1H), 7.58 (d, J=1.59 Hz, 1H), 7.48 (d, J=7.98 Hz, 1H), 7.34 (dt, J=9.90, 2.50 Hz, 1H), 7.18 (dt, J=8.53, 2.57 Hz, 1H), 6.71 (s, 1H), 5.33 (s, 2H), 2.74 (s, 3H), 1.98 (s, 3H), 1.88 (s, 3H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.58 (quintet, J=7.49 Hz, 1F), −113.65 (quartet, J=9.11 Hz, 1F). ES-HRMS m/z 477.0612 (M+H calcd for C₂₂H₂₀BrF₂N₂O₃ requires 477.0620).

Example 588

(+)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

The title compound was prepared as in Example 587, pooling the late-eluting atropisomer (722 mg, 81%). Analytical chiral LC (Chiralpak AD, 4.6 mm×50 mm, 10 μm particle size, 0.5 ml/min ethanol) Retention time: 2.00 min, ee 98%. [α_D=+28.20 (5 mg/ml DMSO, 22° C.). ¹H NMR (400 MHz, DMSO-d₆) δ 8.42 (br qr, J=4.51 Hz, 1H), 7.82 (dd, J=7.92, 1.70 Hz, 1H), 7.68 (dt, J=8.24, 6.58 Hz, 1H), 7.58 (d, J=1.59 Hz, 1H), 7.48 (d, J=7.98 Hz, 1H), 7.34 (dt, J=9.90, 2.50 Hz, 1H), 7.18 (dt, J=8.53, 2.57 Hz, 1H), 6.71 (s, 1H), 5.33 (s, 2H), 2.74 (s, 3H), 1.98 (s, 3H), 1.88 (s, 3H). ¹⁹F-NMR (400 MHz, DMSO-d₆) δ −109.58 (quintet, J=7.49 Hz, 1F), −113.65 (quartet, J=9.11 Hz, 1F). ES-HRMS m/z 477.0614 (M+H calcd for C₂₂H₂₀BrF₂N₂O₃ requires 477.0620).

Example 589

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-chlorobenzamide

Step 1: Preparation of Methyl 3-chloro-4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate

4-Hydroxy-6-methyl-2-pyrone (24.5 g, 193.9 mmol) and methyl-3-amino-2-chlorobenzoate (30 g, 161.6 mmol) were suspended in 75 ml of 1,2-dichlorobenzene in a 250 ml, 3-necked round bottom flask equipped with a J-Kem temperature controller probe, a Dean-Stark trap, and a heating mantle. The reaction was heated to 175° C. for 20 minutes, during which, water and some 1,2-dichlorobenzene was collected in the Dean-Stark trap. The reaction was allowed to cool to about 110° C. At this point, 200 ml of toluene was added. The toluene mixture was allowed to stir for 72 hours at room temperature. A precipitate was collected on a filter pad. The precipitate was filtered and washed 3 times with toluene, 3 times with 50° C. water to remove excess pyrone, and dried in vacuo to give a tan solid (13.0 g, 27% yield). ¹H NMR (300 MHz, CD₃OD) δ 8.26 (d, J=1.81 Hz, 1H), 8.14 (dd, J=8.26, 1.81 Hz, 1H), 7.54 (d, J=8.26, Hz, 1H), 6.14(dd, J=2.42, 1.0 Hz, 1H), 5.83 (d, J=2.42 1H), 4.00 (s, 3H), 1.96 (s, 3H); LC/MS, t_r=1.81 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 294 (M+H).

Step 2: Preparation of Methyl 3-chloro-4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate

Methyl 3-chloro-4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate (from Step 1) (2.4 g, 8.17 mmol) was taken up in DMF (10 ml). 2,4-difluorobenzylbromide (1.05 ml, 8.17 mmol) and K₂CO₃ (1.13 g, 8.17 mmol) were added. The reaction stirred for 6 hours at room temperature. At this time, the reaction was poured into water (200 ml) and extracted with ethyl acetate. The ethyl acetate layer was dried over Na₂SO₄, filtered, and the solvent removed in vacuo to give amber oil (2.62 g, 77% crude yield). LC/MS, t_r=2.79 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 294 (M+H).

Step 3: Preparation of Methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-chlorobenzoate

Methyl 3-chloro-4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (from step 2) (2.60 g, 6.21 mmol) was taken up in CH₂Cl₂ (20 ml). N-bromosuccinimide (1.11 g, 6.21 mmol) was added and the mixture stirred at room temperature for 4 hours. The CH₂Cl₂ is removed in vacuo and the residue is taken up in CH₃CN. The resulting precipitate is collected on a filter pad and washed with CH₃CN to yield a white solid (0.75 g, 24%). ¹H NMR (300 MHz, CDCl₃) δ 8.22 (d, J=1.88 Hz, 1H), 8.06 (dd, J=8.19, 1.75 Hz, 1H), 7.59 (app q, J=8.46 Hz, 1H), 7.33 (d, J=8.19, 1H), 6.96 (dt, J=8.06, 1.21 Hz, 1H), 6.89-6.84 (m, 1H), 6.13 (s, 1H), 5.26 (s, 2H), 3.95 (s, 3H), 1.95 (s, 3H); ES-MS m/z 478 (M+H). ES-HRMS m/z 497.9892 (M+H calcd for C₂₂H₁₆BrClF₂NO₄ requires 497.9914).

Step 4: Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-chlorobenzoic Acid

Methyl-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-chlorobenzoate (2.30 g, 4.61 mmol) was taken up in THF (20 ml) and H₂O (4 ml). 2.5 N NAOH (9.2 ml) was added to the vessel and the reaction stirred overnight to completion. Concentrated HCl was added dropwise until reaction was made acidic (pH=1). H₂O (100 ml) and THF (100 ml) were added to the mixture. The contents were poured into a separatory funnel and the aqueous layer was extracted with ethyl acetate. The organic layer was dried over Na₂SO₄, the solvent removed in vacuo, and the residue was taken up in a 50% mixture of ethyl acetate/hexane. The precipitate was collected on a filter pad to yield a white powder (1.5 g, 67%). ¹H NMR (300 MHz, DMSO) δ 13.59 (1H), 8.16 (d, J=1.81 Hz, 1H), 8.06 (dd, J=6.24, 1.81 Hz, 1H), 7.73 (app q, J=8.46, 1H), 7.68 (d, J=8.26 Hz, 1H), 7.38 (dt, J=9.48, 2.62 Hz, 1H) 7.26-7.18 (m, 1H), 6.80 (s, 1H), 5.39 (s, 2H), 3.93 (s, 3H), 1.96 (s, 3H); ES-MS m/z 483 (M+H). ES-HRMS m/z 483.9749 (M+H calcd for C₂₀H₁₄BrClF₂NO₄ requires 483.9757).

Step 5: 4-[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-chlorobenzoic acid (0.5 g, 1.03 mmol) was taken up in THF (10 ml). 2-Chloro-4,6-dimethoxy-1,3,5-triazine (0.22 g, 1.24 mmol) and N-methyl morpholine (0.34 ml, 3.09 mmol) were added. The mixture stirred at room temperature for 1 hour. At this time, NH₄OH (2.5 ml) was added and the reaction stirred at room temperature for one more hour. To the reaction mixture was added more THF (50 ml) and water (200 ml). The mixture was extracted with ethyl acetate. The ethyl acetate extraction was washed with saturated brine solution. The brine layer was extracted with ethyl acetate. The organic layers were combined, dried over Na₂SO₄, filtered and the solvent was removed in vacuo. The residue was taken up in ethyl acetate and the resulting precipitate was collected on a filter pad to yield a white powder (0.38 g, 76%) ¹H NMR (300 MHz, CD₃OD) δ 8.18 (d, J=1.81 Hz, 1H), 8.02 (dd, J=8.26, 2.01 Hz, 1H), 7.69 (app q, J=8.26 Hz, 1H), 7.55 (d, J=8.06 Hz, 1H) 7.12-7.06 (m, 2H), 6.71 (s, 1H), 5.40 (s, 2H), 2.07 (s, 3H). ES-MS m/z 482 (M+H). ES-HRMS m/z 482.9919 (M+H calcd for C₂₀H₁₅BrClF₂N₂O₃ requires 482.9917).

Example 590

3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(H)-yl]-4-methylbenzamide

Step 1: Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

3-[4-[(2,4-Difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (from above) (7.5 g, 19.4 mmol) and NCS (2.6 g, 19.4 mmol) were taken up in 65° C. dichloroethane (100 ml). A catalytic amount of dichloroacetic acid (2 drops) was added. After two hours the solvent was removed in vacuo and the residue was taken up in diethyl ether. The precipitate was collected on a filter pad and then taken up in 50% ethyl acetate/hexanes to remove residual succinimide. The precipitate was collected on a filter pad and then dried in vacuo to produce a white powder (4.2 g, 52%). ¹H NMR (300 MHz, CD₃OD) δ 8.10 (dd, J=7.85, 1.81 Hz, 1H), 7.83 (d, J=8.26, 1.81 Hz, 1H), 7.40 (app q, J=8.26 Hz, 1H), 7.58 (d, J=7.85 Hz, 1H), 7.13-7.06 (m, 2H), 6.74 (s, 1H), 5.40 (s, 2H), 2.14 (s, 3H), 2.04 (s, 3H); ES-MS m/z 420 (M+H). ES-HRMS m/z 420.0786 (M+H calcd for C₂₁H₁₇ClF₂NO₄ requires 420.0809).

Step 2: 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (1.5 g, 3.57 mmol) was taken up in THF (30 ml). 2-Chloro-4,6-dimethoxy-1,3,5-triazine (0.75 g, 4.28 mmol) and N-methyl morpholine (1.18 ml, 10.72 mmol) were added. The mixture stirred at room temperature for 1 hour. At this time, NH₄OH (7.5 ml) was added and the reaction stirred at room temperature for one more hour. To the reaction mixture was added more THF (100 ml) and water (150 ml). The mixture was extracted with ethyl acetate. The ethyl acetate extraction was washed with saturated brine solution. The brine layer was extracted with ethyl acetate. The organic layers were combined, dried over Na₂SO₄, filtered and the solvent was removed in vacuo. The residue was taken up in ethyl acetate and the resulting precipitate was collected on a filter pad to yield a white powder (1.32 g, 88%) ¹H NMR (300 MHz, CD₃OD) δ 7.96 (dd, J=7.85, 1.81 Hz, 1H), 7.71 (d, J=1.81 Hz, 1H), 7.67 (app q, J=8.06 Hz, 1H), 7.56 (d, J=8.06 Hz, 1H), 7.12-7.06 (m, 2H), 6.74 (s, 1H), 5.40 (s, 2H), 2.13 (s, 3H) 2.05 (s, 3H). ES-MS m/z 419 (M+H). ES-HRMS m/z 419.0979 (M+H calcd for C₂₁H₁₈ClF₂N₂O₃ requires 419.0969).

Example 591

3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

The title compound was prepared from 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (from step 1 above) (1.5 g, 3.57 mmol) in dichloromethane (35 ml). To this mixture, 2.0 M methyl amine in THF (3.6 ml, 7.14 mmol) was added, followed, in order, by EDCI (0.67 g, 4.28 mmol), 1-hydroxybenzotriazole (0.58 g, 4.28 mmol) and triethylamine (0.99 ml, 7.14 mmol). The reaction was stirred at room temperature overnight. The reaction was quenched with NH₄Cl and extracted 3 times with ethyl acetate. The combined organic layer was then washed with saturated NaHCO₃ (aq.) and extracted 3 times with ethyl acetate. The organic layers were combined and washed with H₂O and extracted 3 times with ethyl acetate. The organic layers were combined and dried over Na₂SO₄ and evaporated. The resulting residue was triturated with diethyl ether/hexane to obtain a solid, which was dried in vacuo to give a white solid (1.5 g, 72%). ¹H NMR (300 MHz, CD₃OD) δ 7.90 (dd, J=8.06, 1.81 Hz, 1H), 7.67 (app q, J=6.44 Hz, 1H), 7.55 (d, J=8.06 Hz, 1H), 7.13-7.06 (m, 2H), 6.74 (s, 1H), 5.40 (s, 2H), 2.93 (s, 3H), 2.13 (s, 3H), 2.04 (s, 3H); ES-MS m/z 433 (M+H). ES-HRMS m/z 433.1153 (M+H calcd for C₂₂H₂₀ClF₂N₂O₃ requires 433.1125).

Example 592

N-{3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzyl}propanamide

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with 1-[5-(aminomethyl)-2-fluorophenyl]-3-chloro-4-[(2,4 difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride (250 mg, 0.56 mmol), propionyl chloride (49 μL, 0.56 mmol), triethylamine (195 μL, 1.4 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 5 min the reaction was completed by LC-MS. The reaction mixture was poured into a saturated aqueous NH₄Cl solution. The aqueous mixture was extracted with ethyl acetate. The organic phase was dried with Na₂SO₄ and concentrated in vacuo to obtain the title compound (240 mg, 91%) as a yellow solid. ¹H NMR (400 MHz, (CD₃)₂SO) δ 8.3 (t, J=5.8 Hz, 1H), 7.6 (q, J=8.7 and 6.58 Hz, 1H), 7.38 (d, J=7.78 Hz, 1H), 7.3 (dd, J=2.6 and 7.6 Hz, 1H), 7.22 (d, J=7.51 Hz, 1H), 7.12 (td, J=2.0 and 6.5 Hz, 1H), 6.65 (s, 1H), 5.3 (s, 2H), 4.23 (d, J=3.6 Hz, 2H), 2.1 (q, J=7.7 Hz 2H), 1.98 (s, 3H), 0.98 (t, J=7.5 Hz, 3H) ppm. ES-HRMS m/z 465.1203 (M+H calcd for C₂₃H₂₁ClF₃N₂O₃ requires 465.1187).

Example 593

N-{3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzyl}dimethylurea

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with 1-[5-(aminomethyl)-2-fluorophenyl]-3-chloro-4-[(2,4 difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride (250 mg, 0.56 mmol), dimethylcarbamyl chloride (52 μL, 0.56 mmol), triethylamine (195 μL, 1.4 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 5 min the reaction was completed by LC-MS. The reaction mixture was poured into a saturated aqueous NH₄Cl solution. The aqueous mixture was extracted with ethyl acetate. The organic phase was dried with Na₂SO₄ and concentrated in vacuo to obtain the desired product (245 mg, 86%) as a white solid. ¹H NMR (400 MHz, (CD₃OD) δ 7.61 (q, J=7.9 and 6.7 Hz, 1H), 7.4(m, 1H), 7.3 (d, J=9.3 Hz, 1H), 7.21 (m, 1H), 7.1 (m, 2H), 6.65 (s, 1H), 5.35 (s, 2H), 4.38 (s, 2H), 2.9 (s, 6H), 2.1 (s, 3H) ppm. ES-HRMS m/z 480.1269 (M+H calcd for C₂₃H₂₂ClF₃N₃O₃ requires 480.1296).

Example 594

N-{3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzyl}-2-hydroxyacetamide

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with 1-[5-(aminomethyl)-2-fluorophenyl]-3-chloro-4-[(2,4 difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride (250 mg, 0.56 mmol), acetoxyacetyl chloride (66 μL, 0.62 mmol), triethylamine (195 μL, 1.4 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 5 min the reaction was completed by LC-MS. NaOH (2.5M, 2.24 mmol, 1.0 mL) and MeOH (2.0 mL) was added and stirred for 10 min to give the title compound. The reaction mixture was acidified with concentrated HCl and extracted with ethyl. The organic phase was dried with Na₂SO₄ and concentrated in vacuo to obtain the title compound (217 mg, 78%) of the desired product as a yellow solid. ¹H NMR (400 MHz, (CD₃OD) δ 7.6 (q, J=7.6 and 6.9 Hz, 1H), 7.44 (m, 1H), 7.34 (m, 2H), 7.22 (m, 2H), 6.63 (s, 1H), 5.35 (s, 2H), 4.41 (s, 2H), 4.0 (s, 2H), 2.05 (s, 3H) ppm. ES-HRMS m/z 467.0957 (M+H calcd for C₂₂H₁₉ClF₃N₂O₄ requires 467.0980).

Example 595

N-{3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzyl}-2-hydroxy-2-methylpropanamide

The title compound was prepared essentially as described in Example 594, with 1-chlorocarbonyl-1-methylethyl acetate substituting acetoxyacetyl chloride ¹H NMR (400 MHz, (CDCl₃) δ 9.9 (q, J=8.2 and 6.5 Hz, 1H), 9.7 (t, J=2.6 Hz, 1H), 9.5 (t, J=8.9 Hz, 2H), 9.3 (m, 1H), 9.2 (m, 1H), 8.6 (s, 1H) 7.6 (s, 2H), 6.8 (d, J=15 Hz, 1H), 6.63 (d, J=15 Hz, 1H), 4.42 (d, J=3.2 Hz, 6H), 3.99 (s, 3H) ppm. ES-HRMS m/z 495.1271 (M+H calcd for C₂₄H₂₃ClF₃N₂O₄ requires 495.1293).

Example 596

N¹-{3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzyl}glycinamide Hydrochloride

A 25 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with boc-glycine (105 mg, 0.6 mmol) and 8 mL of DMF. The mixture was cooled to 0° C. and isboutylchloroformate (77.5 μL, 0.6 mmol) was added and stirred for 20 min. 1-[5-(aminomethyl)-2-fluorophenyl]-3-chloro-4-[(2,4 difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride (250 mg, 0.6 mmol) was added and stirred for 3 h. After completion of the reaction by LC-MS, concentrated HCl (2 mL) and 2 mL of methanol was added to remove the boc group. The reaction was stirred for 24 h, neutralized with 2M NaOH and extracted with ethyl acetate. The organic phase was dried with Na₂SO₄ and concentrated in vacuo to obtain the desired product (196 mg, 66%) as an HCl salt. ¹H NMR (400 MHz, (CD₃OD) δ 7.6 (q, J=8 and 6.5 Hz, 1H), 7.5 (m, 1H), 7.3 (m, 2H), 7.0 (m, 2H), 6.63 (s, 1H), 5.35 (s, 2H), 4.4 (q, J=15 and 13.6 Hz, 2H), 3.7 (s, 2H), 2.05 (s, 3H) ppm. ES-HRMS m/z 466.1157 (M+H calcd for C₂₂H₂₀ClF₃N₃O₃ requires 466.1140).

Example 597

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzamide

A 250 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid (3.65 g, 7.8 mmol), 4-methylmorpholine (2.6 mL, 23.4 mmol), 2-chloro-4,6-dimethoxy-1,3,5-triazine (1.64 g, 9.36 mmol) and tetrahydrofuran (40 mL). After stirring the mixture for 30 min at 25° C., NH₄OH (20.0 mL) was added. The mixture was stirred for 30 min and diluted with water. The product precipitated from solution. The precipitated was filtered and washed with water and diethyl ether to give the title compound (2.37 g, 65%) as a white solid. ¹H NMR (400 MHz, (CD₃)₂SO) δ 7.9 (d, J=7.3 Hz, 1H), 7.61 (q, J=8.6 and 6.7 Hz, 1H), 7.5 (m, 2H), 7.3 (t, J=9.6 Hz, 1H), 7.15 (t, J=8.7 Hz, 1H), 6.7 (s, 1H), 5.36 (s, 2H), 2 (s, 3H) ppm. ES-HRMS m/z 469.0172 (M+H calcd for C₂₀H₁₅BrF₃N₂O₃ requires 469.0195).

Example 598

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluoro-N-methylbenzamide

A solution of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid (1 g, 2.1 mmol) in N,N-dimethylformamide (20 mL) was cooled to −10 C. Isobutyl chloroformate (0.27 mL, 2.1 mmol) and N-methyl morpholine (0.23 mL, 2.1 mmol) were added to the reaction vessel. After stirring at −10 C for 20 minutes, a solution of N-methyl amine (2.1 mL, 4.2 mmol, 2 M in THF) was added and the reaction mixture was warmed to room temperature as it stirred for 18 hours. The reaction mixture was concentrated in vacuo, suspended in water, filtered and washed with water, ethyl acetate and diethyl ether. ¹H NMR (400 MHz, CD₃OD) δ 8.03 (dddd, J=3.0, 6.4, 9.2 and 11.6 Hz, 1H), 7.81 (dd, J=3.0 and (0.2 Hz, 1H), 7.66 (q, J=10.4 Hz, 1H), 7.47 (t, J=12 Hz, 1H), 7.06 (t, J=12 Hz, 2H), 6.67 (s, 1H), 5.38 (s, 2H), 2.91 (s, 3H), 2.10 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.50 (1F), −115.97 (1F), −120.16 ppm. ES-HRMS m/z 481.0346 (M+H calcd for C₂₁H₁₇BrF₃N₂O₃ requires 481.0369).

Example 599

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluoro-N,N-dimethylbenzamide

A solution of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid (1 g, 2.1 mmol) in N,N-dimethylformamide (20 mL) was cooled to −10 C. Isobutyl chloroformate (0.27 mL, 2.1 mmol) and N-methyl morpholine (0.23 mL, 2.1 mmol) were added to the reaction vessel. After stirring at −10 C for 20 minutes, a solution of N-methyl amine (2.1 mL, 4.2 mmol, 2 M in THF) was added and the reaction mixture was warmed to room temperature as it stirred for 18 hours. The reaction mixture was concentrated in vacuo and partitioned between water and ethyl acetate. The organic layer was washed with brine and concentrated in vacuo. The solid was chromatographed on silica (95:5 methylene chloride: isopropyl alcohol) to give the desired product as a white powder (0.31 g, 30%). ¹H NMR (400 MHz, CD₃OD) δ 7.64 (m, 1H), 7.50 (dd, J=2.4 and 7.2 Hz, 1H), 7.45 (t, J=9.6 Hz, 1H), 7.04 (t, J=9.2 Hz, 2H), 6.65 (s, 1H), 5.36 (s, 2H), 3.09 (s, 3H), 3.05 (s, 3H), 2.10 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.51 (1F), −115.88 (1 F), −121.90 (1F) ppm. ES-HRMS m/z 495.0508 (M+H calcd for C₂₂H₁₉BrF₃N₂O₃ requires 495.0526).

Example 600

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2-fluoro-5-[(4-methylpiperazin-1-yl)carbonyl]phenyl}-6-methylpyridin-2(1H)-one

Step 1 Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]1-{2-fluoro-5-[(4-methylpiperazin-1-yl)carbonyl]phenyl}-6-methylpyridin-2(1H)-one

To a reaction vessel (borosilicate culture tube) was added 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorobenzoic acid (0.300 g, 0.623 mmol) and 1-hydroxybenzotriazole (0.042 g, 0.45 mmol). N,N-Dimethylformamide (3 mL) was added to the reaction vessel followed by approximately 1.1 g of the polymer bound carbodiimide resin (1.38 mmol/g). Additional N,N-dimethylformamide (2 mL) was then added to the reaction vessel. The parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 15 minutes. N-Methyl amine (1 mL, 2 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature overnight. At this time the reaction was diluted with tetrahydrofuran (20 mL) and treated with approximately 2.0 g of polyamine resin (2.63 mmol/g) and approximately 2.5 g of methylisocyanate functionalized polystyrene (1.5 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature for 3 hours. The reaction vessel was then opened and the solution phase product was separated from the insoluble quenched byproducts by filtration and collection into a vial. After partially evaporation the insoluble byproducts were rinsed with tetrahydrofuran (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial and the resulting solid was triturated with diethyl ether to give an off-white solid. (0.14 g, 41%) ¹H NMR (400 MHz, CD₃OD) δ 7.63 (m, 1H), 7.51 (dd, J=2.2 and 7.2 Hz, 1H), 7.45 (t, J=8.4 Hz, 1H), 7.03 (m, 2H), 6.65 (s, 1H), 5.34 (s, 2H), 3.74 (s, 2H), 3.51 (s, 2H), 2.80 (s, 4H), 2.08 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.31 (1F), −115.72 (1 F), −121.41 (1 F) ppm. ES-HRMS m/z 550.0946 (M+H calcd for C₂₅H₂₄ClF₃N₃O₃ requires 550.0948).

Example 601-603

By following the method of Example 600 and replacing N-methylamine with the appropriate amine, the compounds of Examples 601-603 are prepared.

Compound			%		M + H
No.	R1	R2	Yield	MF	Requires	ESHRMS m/z
Ex. 601	CH2CH2O—	CH2CH2—	98	C24H21BrF3N2O4	537.0631	537.0620
Ex. 602	CH3	CH2CH2OH	43	C23H21BrF3N2O4	525.0631	525.0618
Ex. 603	H	CH2C(CH3)2OH	65	C24H23BrF3N2O4	539.0783	539.0788

Example 604

Methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzoate

Step 1 Preparation of 4-amino-3-fluorobenzoic Acid

3-Fluoro-4-aminobenzoic acid was prepared as described in the literature. (Schmelkes, F. C.; Rubin, M. J. Am. Chem. Soc. 1944, 66, 1631-2.)

Step 2 Preparation of Methyl 4-amino-3-fluorobenzoate

A 250 mL 3-necked round bottomed flask equipped with a nitrogen inlet, stirbar, addition funnel and thermocouple was charged with 4-amino-3-fluorobenzoic acid (11.8 g, 76 mol) and methanol (100 mL). The system was cooled to 0 C and acetyl choride (7.6 mL, 107 mol) was added dropwise. The system was warmed to room temperature, the addition funnel was replaced with a reflux condenser, and was heated to reflux for 6 h. The reaction mixture was cooled to room temperature, quenched with saturated aqueous NaHCO₃, and extracted with ethyl acetate. The organic extract was washed with brine and concentrated in vacuo to give methyl methyl 4-amino-3-fluorobenzoate as an tan solid (8.2 g, 64%). ¹H NMR (400 MHz, CD₃OD) δ 7.56 (dd, J=1.6 and 8.0 Hz, 1H), 7.52 (dd, J=1.9 and 12 Hz, 1H), 6.76 (t, J=8.4 Hz, 1H), 3.81 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −139.05 (1F) ppm. ES-HRMS m/z 170.0565 (M+H calcd for C₈H₉FNO₂ requires 170.0612).

Step 3 Preparation of Methyl 3-fluoro-4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate

A 250 mL round bottomed flask equipped with stirbar, Dean-Stark trap and reflux condensor was charged with the product of Step 2 (8 g, 47.3 mmol), 4-hydroxy-6-methyl-2-pyrone (12 g, 84.6 mmol), and N-methyl-2-pyrrolidine (8 mL). The system was immersed in a 150 C oil bath for 2 hours and was then cooled to room temperature. The reaction mixture was washed with aqueous K₂CO₃ (8.5 g, 200 mL water). The aqueous layer was washed with ethyl acetate and then was acidified to pH 4-5 with glacial HOAc. This was extracted with ethyl acetate, which was then concentrated in vacuo. The viscous oil was triturated with acetonitrile and filtered to the title compound as a tan solid (2.3 g, 17%). ¹H NMR (400 MHz, CD₃OD) δ 7.98 (dd, J=1.8 and 8.0 Hz, 1H), 7.91 (dd, J=1.7 and 10 Hz, 1H), 7.46 (t, J=8 Hz, 1H), 6.09 (dd, J=0.9 and 2.4 Hz, 1H), 5.77 (d, J=2.7 Hz, 1H), 3.94 (s, 3H), 1.97 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −123.00 (1F) ppm. ES-HRMS m/z 278.0781 (M+H calcd for C₁₄H₁₃FNO₄ requires 278.0823).

Step 4 Preparation of Methyl 4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzoate

A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the product of Step 4 (2.3 g, 8.3 mmol) and N,N-dimethyl formamide (20 mL). 1,8-diazabicyclo[5.4.0]undec-7-ene (1.4 mL, 9.1 mmol) was added followed by 2,4-difluorobenzyl bromide (1.2 mL, 9.1 mmol). The reaction mixture was stirred at 60 C for 3 h, was poured into saturated aqueous NaHCO₃ and was extracted with ethyl acetate. The organic layer was washed with brine and concentrated in vacuo. The solid was triturated with acetonitrile and filtered to give the title compound (2.15 g, 64%). ¹H NMR (400 MHz, CD₃OD) δ 7.99 (dd, J=1.7 and 8.4 Hz, 1H), 7.93 (dd, J=1.8 and 10.4 Hz, 1H), 7.55 (m, 1H), 7.48 (t, J=6.8 Hz, 1H), 7.02 (m, 2H), 6.18 (dd, J=1.3 and 2.76 Hz, 1H), 6.02 (d, J=2.7 Hz, 1H), 5.14 (s, 2H), 3.94 (s, 3H), 1.98 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.34 (1F), −115.97 (1 F), −122.98 (1 F) ppm. ES-HRMS m/z 404.1133 (M+H calcd for C₂₁H₁₇F₃NO₄ requires 404.1104).

Step 5 Preparation of Methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzoate

A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the product of Step 4 (2.15 g, 5.3 mmol) and N-methyl-2-pyrrolidine (15 mL). After cooling to 0 C, a solution of N-bromo succinimide (1.03 g, 5.8 mmol) in 10 mL of N-methyl-2-pyrrolidine was added over 15 minutes. After 15 additional minutes, the reaction mixture was warmed to room temperature and was stirred for 1 hour. The mixture was then poured into saturated aqueous NaHCO₃ and extracted with ethyl acetate. The organic layer was washed with brine and concentrated in vacuo. The residue was triturated with acetonitrile and filtered to give the title compound as a white powder (1.5 g, 59%). ¹H NMR (400 MHz, CD₃OD) δ 8.00 (dd, J=2.0 and 8.4 Hz, 1H), 7.95 (dd, J=1.7 and 10 Hz, 1H), 7.64 (q, J=8.8 and 14.4 Hz, 1H), 7.51 (t, J=7.6 Hz, 1H), 7.04 (t, J=8.4 Hz, 2H), 6.66 (s, 1H), 5.36 (s, 2H), 3.95 (s, 3H), 2.01 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.50 (1F), −115.97 (1 F), −123.01 (1 F) ppm. ES-HRMS m/z 484.0169 (M+H calcd for C₂₁H₁₆BrF₃NO₄ requires 484.0192).

Example 605

4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic Acid

Preparation of 4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid. Methyl-4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoate (30.4 g, 70.1 mmol) was suspended in methanol (150 mL) and dioxane (150 mL). 2.5N NaOH (30.8 mL, 77.08 mmol) was added. The resulting mixture was heated to 50° C. for 8.0 hours. The reaction was partially concentrated and the heterogenous mixture was acidified (pH 2) with 1N HCl. The precipitate was collected by filtration washing with H₂O and diethyl ether to afford a white solid (29.2 g, 99%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.88 (d, J=8.3 Hz, 2H), 7.63 (app q, J=7.9 Hz, 1H), 7.31 (dt, J=2.4, 9.9 Hz, 1H), 7.18 (app d, J=8.3 Hz, 2H), 7.17-7.12 (m, 1H), 6.60 (s, 1H), 5.35 (s, 2H), 5.27 (s, 2H), 2.28 (s, 3H). ES-HRMS m/z 420.0821 (M+H calcd for C₂₁H₁₇ClF₂NO₄ requires 420.0809).

Example 606

4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide

Preparation of 4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzamide. 4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid (12.0 g, 28.58 mmol) was suspended in tetrahydrofuran (100 mL). 2-Chloro-4,6-dimethoxy-1,3,5-triazine (6.02 g, 34.3 mmol) was added followed by 4-methylmorpholine (9.43 mL, 85.74 mmol). The resulting mixture was stirred at room temperature for 1.5 hours at which time NH₄OH (50.0 mL) was added. The resulting mixture was stirred at room temperature for 1 hour and then partially concentrated. The precipitate was collected by filtration washing with H₂O and diethyl ether to provide an off-white solid (12.11 g, >100%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.91 (br s, 1H), 7.80 (d, J=8.3 Hz, 2H), 7.63 (app q, J=7.9 Hz, 1H), 7.31 (dt, J=2.6, 10.5 Hz, 1H), 7.17-7.12 (m, 1H), 7.13 (app d, J=8.3 Hz, 2H), 6.59 (s, 1H), 5.32 (s, 2H), 5.27 (s, 2H), 2.28 (s, 3H). ES-HRMS m/z 419.0968 (M+H calcd for C₂₁H₁₈ClF₂N₂O₃ requires 419.0969).

Example 607

4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylbenzamide

Preparation of 4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}}-N,N-dimethylbenzamide. 4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid (2.00 g, 4.76 mmol) was suspended in N,N-dimethylformamide (20 mL). 1-Hydroxybenzotriazole (0.773 g, 5.72 mmol) was added followed by 4-methylmorpholine (1.57 mL, 14.28 mmol), dimethylamine (7.14 mL, 2.0 M in tetrahydrofuran, 14.28 mmol) and then 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (1.28 g, 6.66 mmol). The resulting mixture was stirred at room temperature for 3 hours at which time the reaction was diluted with H₂O (75 mL). The reaction mixture was then extracted with ethyl acetate. The combined organic extracts were washed with saturated NaHCO₃, brine, dried over Na₂SO₄, filtered and concentrated. The resulting solid was washed with ethyl acetate to provide the title compound as a white solid (1.67 g, 78%). ¹H NMR (400 MHz, CDCl₃) δ 7.53 (app q, J=7.8 Hz, 1H), 7.33 (d, J=8.3 Hz, 2H), 7.16 (d, J=8.3 Hz, 2H), 6.95-6.90 (m, 1H), 6.84 (app dt, J=2.5, 9.4 Hz, 1H), 6.02 (s, 1H), 5.35 (s, 2H), 5.19 (s, 2H), 2.97-2.93 (br m, 6H), 2.26 (s, 3H). ES-HRMS m/z 447.1246 (M+H calcd for C₂₃H₂₂ClF₂N₂O₃ requires 447.1282).

Example 608

4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxy-2-methylpropyl)benzamide

Preparation of 4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxy-2-methylpropyl)benzamide. 4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid (2.00 g, 4.76 mmol) was suspended in N,N-dimethylformamide (10 mL). 1-Hydroxybenzotriazole (0.772 g, 5.71 mmol) was added followed by 4-methylmorpholine (1.57 mL, 14.28 mmol), 1-amino-2-methyl-2-propanol hydrochloride (1.49 g, 11.90 mmol) and then 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (1.28 g, 6.66 mmol). The resulting mixture was stirred at room temperature for 2 days at which time the reaction was diluted with H₂O (50 mL). The reaction mixture was then extracted with ethyl acetate. The combined organic extracts were washed with saturated NaHCO₃, brine, dried over Na₂SO₄, filtered and concentrated. The resulting solid was washed with diethyl ether to provide the title compound as a tan solid (2.08 g, 89%). ¹H NMR (400 MHz, CDCl₃) δ 7.72 (d, J=8.2 Hz, 2H), 7.51 (app q, J=7.7 Hz, 1H), 7.25-7.21 (m, 1H), 7.10 (d, J=8.2 Hz, 2H), 6.93 (app dt, J=1.6, 8.3, 9.4 Hz, 1H), 6.87-6.82 (m, 1H), 6.01 (s, 1H), 5.32 (s, 2H), 5.19 (s, 2H), 3.42 (d, J=5.9 Hz, 2H), 2.26 (s, 3H), 1.23 (s, 6H). ES-HRMS m/z 491.1522 (M+H calcd for C₂₅H₂₆ClF₂N₂O₄ requires 491.1544).

Example 609

N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-2-hydroxyacetamide

Step 1. Preparation of 1-[4-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Example 244 (0.250 g, 0.556 mmol) was suspended in tetrahydrofuran (2.0 mL) and cooled in an ice-bath. Borane dimethyl sulfide (0.500 mL, 2.0 M in tetrahydrofuran, 1.00 mmol) was added. The resulting mixture was heated to reflux overnight and then cooled in an ice-bath. The reaction was quenched by the addition of 6.0 N HCl (5.0 mL) then washed with ethyl acetate. The aqueous layer was made alkaline with 2.5 N NaOH and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered and concentrated to provide an off-white solid (0.180 g, 74%). ¹H NMR (400 MHz, CDCl₃) δ 7.58 (app q, J=7.8 Hz, 1H), 7.44 (app d, J=8.2 Hz, 2H), 7.10 (d, J=8.2 Hz, 2H), 6.95 (app dt, J=1.5, 8.5 Hz, 1H), 6.88-6.83 (m, 1H), 6.06 (s, 1H), 5.24 (s, 2H), 3.93 (s, 2H), 1.96 (s, 3H).

Step 2. Preparation of 2-({4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}amino)-2-oxoethyl

Acetoxyacetic acid (0.037 g, 0.310 mmol) was dissolved in dichloromethane (2.0 mL). 1-hydroxybenzotriazole (0.021 g, 0.155 mmol) was added followed by 3-(1-cyclohexylcarbodiimide)propyl-functionalized silica gel (1.00 g, 0.620 mmol, loading=0.64 mmol/g). After stirring at room temperature for 15 minutes, 1-[4-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (Step 1) (0.180 g, 0.310 mmol) in dichloromethane (2.0 mL) was added. The resulting mixture was stirred at room temperature overnight, at which time the reaction mixture was filtered and concentrated. Chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) provided a white solid (0.130 g, 78%). ¹H NMR (400 MHz, CDCl₃) δ 7.58 (app q, J=7.8 Hz, 1H), 7.33 (d, J=8.3 Hz, 2H), 7.05 (app d, J=8.3 Hz, 2H), 6.97-6.92 (m, 1H), 6.88-6.83 (m, 1H), 6.08 (s, 1H), 5.24 (s, 2H), 4.58 (s, 2H), 4.44(d, J=6.0 Hz, 2H), 2.13 (s, 3H), 1.95 (s, 3H).

Step 3. Preparation of N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-2-hydroxyacetamide. 2-({4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}amino)-2-oxoethyl (Step 2) (0.130 g, 0.243 mmol) was dissolved in methanol (5 mL) and H₂O (1 mL). K₂CO₃ (0.055 g, 0.398 mmol) was added and the resulting mixture was stirred at room temperature for 2 hours. The mixture was then concentrated and the residue was partitioned between H₂O and ethyl acetate. The organic layer was removed and the aqueous layer was further extracted with ethyl acetate. The combined organic layer were washed with brine, dried over Na₂SO₄, filtered and concentrated to provide an off-white solid (0.100 g, 84%). ¹H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=7.7 Hz, 1H), 7.43 (t, J=5.8 Hz, 1H), 7.33 (d, J=8.2 Hz, 2H), 7.04 (app d, J=8.3 Hz, 2H), 6.98-6.93 (m, 1H), 6.88-6.83 (m, 1H), 6.11 (s, 1H), 5.24 (s, 2H), 4.41 (d, J=6.0 Hz, 2H), 3.87 (s, 2H), 1.96 (s, 3H). ES-HRMS m/z 493.0575 (M+H calcd for C₂₂H₂₀BrF₂N₂O₄ requires 493.0569).

Example 610

3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide

Example 291 (2.00 g, 4.93 mmol) and 2-chloro-4,6-dimethoxy-1,3,5-triazine (1.04 g, 5.91 mmol) were suspended in tetrahydrofuran (20 mL). 4-Methylmorpholine (1.6 mL, 14.79 mmol) was added. The resulting mixture was stirred for 1.5 hours at room temperature. NH₄OH (10 mL, 148.00 mmol) was added and the reaction was stirred for 0.5 hours at room temperature. H₂O (50 mL) and tetrahydrofuran (50 mL) were added and the organic layer was separated. The aqueous phase was extracted with ethyl acetate (75 mL) and the combined organics were washed with saturated Na₂CO₃ (50 mL), 1N HCl (50 mL), and brine (50 mL). The organic phase was dried over Na₂SO₄ and evaporated. The resulting solid was washed with diethyl ether to give a white solid (1.96 g, 98%). ¹H NMR (400 MHz, DMF-d₆) δ 8.24 (br s, 1H), 8.10 (dt, J=1.21, 7.79 Hz, 1H), 7.90 (t, J=1.88 Hz, 1H), 7.79 (app dt, J=6.58, 8.59 Hz, 1H), 7.66 (t, J=7.79 Hz, 1H), 7.57-7.55 (m, 1H), 7.46 (br s, 1H), 7.33 (ddd, J=2.55, 9.26, 11.82 Hz, 1H) 7.24-7.19 (m, 1H), 6.78 (s, 1H), 5.44 (s, 2H), 2.04 (s, 3H). ES-HRMS m/z 405.0835 (M+H calcd for C₂₀H₁₆BrF₂N₂03 requires 405.0812).

Example 611

1-(4-aminobenzyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 1-tert-butyl-4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenylcarbamate

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid (8.00 g, 17.23 mmol) was suspended in 1:1 acetonitrile:t-butanol (172 mL). Diphenylphosphoryl azide (5.69 g, 20.68 mmol) and triethylamine (2.08 g, 20.68 mmol) were added. The reaction was heated to reflux for 1.5 hours. The reaction mixture was cooled to room temperature, concentrated and subjected to chromatography (on silica, ethyl acetate with 10% methanol/hexanes) to afford an off-white solid (6.14 g, 66%).

Step 2: 1-tert-butyl-4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenylcarbamate (Step 1) (6.14 g, 11.47 mmol) was suspended in 4N HCl in dioxane (5.74 mL, 22.94 mmol). The reaction mixture was stirred at room temperature for 1 hour then diluted with diethyl ether. The precipitate was collected by filtration and washed with diethyl ether (3×30 mL) to afford a tan solid (3.45 g, 69%). ¹H NMR (400 MHz, DMF-d₆) δ 7.64 (app dt, J=6.58, 8.59 Hz, 1H), 7.31 (ddd, J=2.55, 9.53, 10.61 Hz, 1H) 7.29-7.12 (m, 5H), 6.56 (s, 1H), 5.28 (s, 2H), 5.27 (s, 2H), 2.28 (s, 3H). ES-HRMS m/z 435.0516 (M+H calcd for C₂₀H₁₈BrF₂N₂O₂ requires 435.0514).

Example 612

1-(3-aminobenzyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

By following the method for Example 611 and substituting 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid for 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoic acid, the title compound was prepared (2.65 g, 67%). ¹H NMR (400 MHz, DMF-d₆) δ 7.64 (app dt, J=6.58, 8.59 Hz, 1H), 7.39 (t, J=7.79 Hz, 1H), 7.32 (ddd, J=2.55, 9.53, 10.61 Hz, 1H) 7.18-7.08 (m, 3H), 6.96 (s, 1H), 6.58 (s, 1H), 5.30 (s, 2H), 5.27 (s, 2H), 2.29 (s, 3H). ES-HRMS m/z 435.0513 (M+H calcd for C₂₀H₁₈BrF₂N₂O₂ requires 435.0514).

Example 613

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)acetamide

To a reaction vessel (borosilicate culture tube) was added Example 611 (0.300 g, 0.689 mmol) and dichloromethane (3.0 mL). A stock solution of N-methylmorpholine (0.30 M, 3.0 mL) was added and the parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 10 minutes. Acetyl chloride (0.074 mL, 1.033 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature for 1.5 hours. At this time the reaction was diluted with dichloromethane (15 mL) and treated with approximately 2.1 g of polyamine resin (2.63 mmol/g) and approximately 3.8 g of methylisocyanate functionalized polystyrene (1.10 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature overnight. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with dichloromethane (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial to afford a white solid (0.135 g, 41%). ¹H NMR (400 MHz, DMF-d₆) δ 7.75 (app dt, J=6.58, 8.59 Hz, 1H), 7.63 (d, J=8.59 Hz, 1H), 7.30 (ddd, J=2.55, 9.53, 10.61 Hz, 1H), 7.22-7.14 (m, 3H), 6.60 (s, 1H), 5.37 (s, 4H), 2.40 (s, 3H), 2.06 (s, 3H). ES-HRMS m/z 477.0600 (M+H calcd for C₂₂H₂₁BrF₂N₂O₃ requires 477.0620). Preparation of Examples 614-616

By following the method for Example 613 and replacing acetyl chloride with the appropriate acid chloride or sulfamoyl chloride, the compounds of Examples 614-616 are prepared. The deprotection of the protected intermediate was accomplished with 1M K₂CO₃ in methanol to afford the title compound.

Compound		%		M + H
No.	R	Yield	MF	Requires	ES-HRMS m/z
Ex. 614	CH2OH	65	C22H20BrF2N2O4	493.0569	493.0593
Ex. 615	CH2OCOCH3	43	C24H22BrF2N2O5	535.0675	535.0702
Ex. 616	SO2N(CH3)2	43	C22H23BrF2N3O4S	542.0555	542.0572

Example 617

N-(3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)acetamide

To a reaction vessel (borosilicate culture tube) was added Example 612 (0.300 g, 0.689 mmol) and dichloromethane (3.0 mL). A stock solution of N-methylmorpholine (0.30 M, 3.0 mL) was added and the parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 10 minutes. Acetyl chloride (0.074 mL, 1.033 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature for 1.5 hours. At this time the reaction was diluted with dichloromethane (15 mL) and treated with approximately 2.1 g of polyamine resin (2.63 mmol/g) and approximately 3.8 g of methylisocyanate functionalized polystyrene (1.10 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature overnight. The reaction vessel was then opened and the solution phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with dichloromethane (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial to afford a white solid (0.167 g, 51%). ¹H NMR (400 MHz, DMF-d₆) δ 7.77 (app dt, J=6.58, 8.59 Hz, 1H), 7.69 (d, J=8.32 Hz, 1H), 7.41 (br s, 1H), 7.34-7.17 (m, 3H), 6.88 (d, J=7.65 Hz, 1H), 6.63 (s, 1H), 5.39 (s, 3H), 5.38 (s, 2H), 2.40 (s, 3H), 2.06 (s, 3H). ES-HRMS m/z 477.0620 (M+H calcd for C₂₂H₂₁BrF₂N₂O₃ requires 477.0620). Preparation of Example 618-620

By following the method for Example 617 and replacing acetyl chloride with the appropriate acid chloride or sulfamoyl chloride, the compounds of Examples 618-620 are prepared. The deprotection of the protected intermediate was accomplished with 1M K₂CO₃ in methanol to afford the title compound.

		%		M + H
Compound No.	R	Yield	MF	Requires	ES-HRMS m/z
Ex. 618	CH2OH	72	C22H20BrF2N2O4	493.0569	493.0604
Ex. 619	CH2OCOCH3	53	C24H22BrF2N2O5	535.0675	535.0692
Ex. 620	SO2N(CH3)2	21	C22H23BrF2N3O4S	542.0555	542.0567

Example 621

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N′-methylurea

Preparation of (4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N′-methylurea. EXAMPLE 160 (150 mg, 0.33 mmol) was dissolved in N,N-dimethylacetamide (5 mL) and cooled to 0° C. 4-Nitrophenyl chloroformate (100 mg, 0.5 mmol) was added, followed by N,N-diisopropylethylamine (0.15 mL, 0.85 mmol) and the reaction was stirred at 0° C. for 5 minutes. N-Methylamine (0.5 mL, 1.0 mmol, 2M in tetrahydrofuran) was added and the reaction was allowed to reach ambient temperature and stirred for 1 hour. The reaction was then diluted with tetrahydrofuran (40 mL) and polyamine resin (1.3 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (1 g, 1.38 mmol/g) were added. The mixture was shaken for 16 hours at ambient temperature, filtered, and the resulting filtrate concentrated to an oil that was triturated with ether. The resulting white solid was collected, washed with ether, and dried (87 mg, 52%). ¹H NMR (400 MHz, CD₃OD) δ 7.61 (app q, J=8.4 Hz, 1H); 7.24 (d, J=8.0 Hz, 2H), 7.07 (d, J=8.0 Hz, 2H), 7.02 (app t, J=8.4 Hz, 2H), 6.47 (s, 1H), 5.39 (s, 2H), 5.28 (s, 2H), 4.26 (s, 2H); 2.68 (s, 3H); 2.34 (s, 3H). ES-HRMS m/z 506.0862 (M+H calcd for C₂₃H₂₃BrF₂N₃O₃ requires 506.0885).

Example 622

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N′-(2-hydroxy-2-methylpropyl)urea

Preparation of N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N′-(2-hydroxy-2-methylpropyl)urea. EXAMPLE 160 (300 mg, 0.67 mmol) was dissolved in N,N-dimethylacetamide (5 mL) and cooled to 0° C. 4-Nitrophenyl chloroformate (200 mg, 1.0 mmol) was added, followed by N,N-diisopropylethylamine (0.3 mL, 1.7 mmol) and the reaction was stirred at 0° C. for 5 minutes. 3-Amino-2-methyl-2-propanol (248 mg, 2.0 mmol) was added and the reaction was allowed to reach ambient temperature and stirred for 3 h. The reaction was then diluted with tetrahydrofuran (40 mL) and polyamine resin (1.3 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (1 g, 1.38 mmol/g) were added. The mixture was shaken for 16 hours at ambient temperature, filtered, and the resulting filtrate concentrated to an oil that was triturated with ether. The resulting white solid was purified by chromatography (silica gel, hexane/ethyl acetate/methanol) followed by reversed phase chromatography (C₁₈, 0.1% aqueous trifluoroacetic acid/acetonitrile) to yield an off-white solid (43 mg, 11%). ¹H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=8.0 Hz, 1H); 7.12 (d, J=8.4 Hz, 2H), 6.97 (d, J=8.0 Hz, 2H), 7.02 (app dt, J=1.6, 8.0 Hz, 2H), 6.83-6.88 (m, 1H), 6.06 (s, 1H), 5.26 (s, 2H), 5.21 (s, 2H); 4.22 (s, 2H); 3.09 (s, 2H); 2.30 (s, 3H); 1.14 (s, 6H). ES-HRMS m/z 564.1279 (M+H calcd for C₂₆H₂₉BrF₂N₃O₄ requires 564.1304).

Example 623

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)piperidine-1-carboxamide

By following the general method for Example 622 and substituting piperidine (170 mg, 2.0 mmol) for 3-amino-2-methyl-2-propanol the title compound was prepared and purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an oil that was triturated with ether to afford a white solid (107 mg, 28%). ¹H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=8.0 Hz, 1H); 7.23 (d, J=8.4 Hz, 2H), 7.11 (d, J=8.0 Hz, 2H), 7.02 (app t, J=8.0 Hz, 2H), 6.81-6.88 (m, 1H), 5.97 (s, 1H), 5.32 (s, 2H), 5.19 (s, 2H); 4.37 (s, 2H); 3.34-3.28 (m, 4H); 2.29 (s, 3H); 1.68-1.50 (m, 6H). ES-HRMS m/z 560.1365 (M+H calcd for C₂₇H₂₉BrF₂N₃O₃ requires 560.1355).

Example 624

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)morpholine-4-carboxamide

By following the general method for Example 622 and substituting morpholine (175 mg, 2.0 mmol) for 3-amino-2-methyl-2-propanol the title compound was prepared and purified by chromatography (silica gel, hexane/ethyl acetate/methanol) followed by reversed phase chromatography (C₁₈, 0.1% aqueous trifluoroacetic acid/acetonitrile) to yield an off-white solid (51 mg, 13%). ¹H NMR (400 MHz, CDCl₃) δ 7.55 (app q, J=8.0 Hz, 1H); 7.17 (d, J=8.4 Hz, 2H), 7.01 (d, J=8.0 Hz, 2H), 6.94(app dt, J=2.4, 8.0 Hz, 2H), 6.82-6.87 (m, 1H), 6.02 (s, 1H), 5.27 (s, 2H), 5.19 (s, 2H); 4.33 (s, 2H); 3.65-3.62 (m, 4H); 3.34-3.36 (m, 4H); 2.28 (s, 3H). ES-HRMS m/z 562.1152 (M+H calcd for C₂₆H₂₇BrF₂N₃O₄ requires 562.1148).

Example 625

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)piperazine-1-carboxamide Hydrochloride

By following the general method for Example 622 and substituting 1-Boc-piperazine (372 mg, 2.0 mmol) for 3-amino-2-methyl-2-propanol the title compound was prepared from its N-t-butoxycarbonyl protected intermediate that was purified by chromatography (silica gel, hexane/ethyl acetate/methanol). Deprotection was accomplished with 4N HCl in dioxane to afford the title compound as its hydrochloride salt (78 mg, 19%). ¹H NMR (400 MHz, CD₃OD) δ 7.61 (app q, J=7.6 Hz, 1H); 7.26 (d, J=8.4 Hz, 2H), 7.07 (d, J=8.4 Hz, 2H), 7.08-7.00 (m, 2H), 6.48 (s, 1H), 5.41 (s, 2H), 5.28 (s, 2H); 4.31 (s, 2H); 3.65-3.62 (m, 4H); 3.21-3.17 (m, 4H); 2.35 (s, 3H). ES-HRMS m/z 561.1318 (M+H calcd for C₂₆H₂₈BrF₂N₄O₃ requires 561.1307).

Example 626

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N′-(2-hydroxyethyl)urea

By following the general method for Example 622 and substituting ethanolamine (121 mg, 2.0 mmol) for 3-amino-2-methyl-2-propanol the title compound was prepared and purified by chromatography (silica gel, hexane/ethyl acetate/methanol) to yield an off-white solid (130 mg, 36%). ¹H NMR (400 MHz, CDCl₃) δ 7.54 (app q, J=7.6 Hz, 1H); 7.13 (d, J=8.4 Hz, 2H), 6.95 (d, J=8.0 Hz, 2H), 6.96-6.92 (m, 1H); 6.83-6.88 (m, 1H), 6.09 (s, 1H), 5.26 (s, 2H), 5.21 (s, 2H); 4.24 (s, 2H); 3.56 (t, J=4.8 Hz, 2H); 3.21 (t, J=4.8 Hz, 2H); 2.31 (s, 3H). ES-HRMS m/z 536.0948 (M+H calcd for C₂₄H₂₅BrF₂N₃O₄ requires 536.0991).

Example 627

N′-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N,N-dimethylurea

By following the general method for Example 622 and substituting N,N-dimethylamine (1.0 mL, 2.0 mmol, 2M in tetrahydrofuran) for 3-amino-2-methyl-2-propanol the title compound was prepared and purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an oil that was triturated with ether to afford a white solid (65 mg, 19%). 1H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=8.0 Hz, 1H); 7.22 (d, J=8.0 Hz, 2H), 7.10 (d, J=8.0 Hz, 2H), 6.93 (app dt, J=2.0, 8.0 Hz, 1H); 6.87-6.81 (m, 1H); 5.97 (s, 1H), 5.31 (s, 2H), 5.19 (s, 2H); 4.36 (s, 2H); 2.89 (s, 6H); 2.28 (s, 3H). ES-HRMS m/z 520.1072 (M+H calcd for C₂₄H₂₅BrF₂N₃O₃ requires 520.1042).

Example 628

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-4-hydroxypiperidine-1-carboxamide

By following the general method for Example 622 and substituting 4-Hydroxypiperidine (202 mg, 2.0 mmol) for 3-amino-2-methyl-2-propanol the title compound was prepared and purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an oil that was triturated with ether to afford a white solid (41 mg, 11%). ¹H NMR (400 MHz, CDCl₃) δ 7.56 (app q, J=8.0 Hz, 1H); 7.20 (d, J=7.6 Hz, 2H), 7.06 (d, J=8.0 Hz, 2H), 6.94 (app t, J=8.0 Hz, 1H); 6.84 (app t, J=8.0 Hz, 1H); 5.99 (s, 1H), 5.29 (s, 2H), 5.19 (s, 2H); 4.34 (s, 2H); 3.84-3.70 (m, 3H); 3.04-2.92 (m, 3H); 2.28 (s, 3H); 1.84-1.81 (m, 2H); 1.47-1.44 (m, 2H). ES-HRMS m/z 576.1348 (M+H calcd for C₂₇H₂₉BrF₂N₃O₄ requires 576.1304).

Example 629

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylbenzenesulfonamide

Step 1: Preparation of 4-Bromomethyl-N,N-dimethylbenzenesulfonamide

4-(Bromomethyl)benzenesulfonyl chloride (5.0 g, 18.6 mmol) was dissolved in tetrahydrofuran. N,N-dimethylamine (7.7 mL, 15.5 mmol, 2M in tetrahydrofuran) and and N,N-diisopropylethylamine (3.5 mL, 20.1 mmol) were added, and the reaction was allowed to stir at ambient temperature for 2 hours. The reaction was concentrated to an oil that was partitioned between water and ethyl acetate and extracted with ethyl acetate. The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The resulting filtrate was concentrated to an oil which deposited needles that were a mixture of the title compound and 4-chloromethyl N,N-dimethylbenzenesulfonamide The resulting needles were collected and dried (2.3 g, 44%). ES-MS m/z 534 (M+H) and 578 (M+H).

Step 2: Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylbenzenesulfonamide. 3-bromo-4-(2,4-difluorophenoxy)-6-methylpyridin-2(1H)-one (300 mg, 0.91 mmol) was suspended in 1,4-dioxane (50 mL). 4-(Bromomethyl)-N,N-dimethylbenzenesulfonamide (from step 1) (300 mg, 1.09 mmol) was added followed by sodium hydride (45 mg, 1.09 mmol, 60% in mineral oil). The reaction was heated to 80° C. and stirred for 16 hours after which more sodium hydride (45 mg, 1.09 mmol, 60% in mineral oil) and sodium iodide (150 mg, 1.0 mmol) were added. The reaction was allowed to stir at 80° C. for 4 hours more. The reaction was then filtered through Celite®0 and the filtrate was concentrated to an oil that was purified by chromatography (silica gel, hexane/ethyl acetate) followed by reversed phase chromatography (C₁₈, 0.1% aqueous trifluoroacetic acid/acetonitrile) to yield an off-white solid (41 mg, 8%). ¹H NMR (400 MHz, CDCl₃) δ 7.71 (d, J=8.4 Hz, 2H); 7.57 (app q, J=7.6 Hz, 1H); 7.29 (d, J=8.0 Hz, 2H); 6.95 (app dt, J=2.0, 8.0 Hz, 1H), 6.88-6.83 (m, 1H); 6.05 (s, 1H), 5.42 (s, 2H), 5.22 (s, 2H); 2.69 (s, 6H); 2.29 (s, 3H). ES-HRMS m/z 527.0439 (M+H calcd for C₂₂H₂₂Br₂F₂N₂O₄S requires 527.0446).

Example 630

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)benzenesulfonamide

Step 1: Preparation of 4-Bromomethyl-N-(2-hydroxyethyl)benzenesulfonamide

4-(Bromomethyl)benzenesulfonyl chloride (5.0 g, 18.6 mmol) was dissolved in tetrahydrofuran. Ethanolamine (1.1 mL, 18.6 mmol) and and N,N-diisopropylethylamine (3.9 mL, 22.3 mmol) were added, and the reaction was allowed to stir at ambient temperature for 30 minutes. The reaction was concentrated to an oil that was partitioned between water and ethyl acetate and extracted with ethyl acetate. The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The resulting filtrate was concentrated to an oil that was a mixture of the title compound and 4-chloromethyl N-(2-hydroxyethyl)benzenesulfonamide. The resulting oil was dried in vacuo (3.7 g, 68%). ES-MS m/z 250 (M+H) and 294 (M+H).

Step 2: Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)benzenesulfonamide

The title compound was prepared essentially according to the procedure described in Step 2 of Example 629, using 4-Bromomethyl-N-(2-hydroxyethyl)benzenesulfonamide (from step 1). ¹H NMR (400 MHz, CDCl₃) δ 7.81 (d, J=8.4 Hz, 2H); 7.61 (app q, J=7.6 Hz, 1H); 7.30 (d, J=8.4 Hz, 2H); 6.95 (app t, J=8.4 Hz, 2H), 6.53 (s, 1H), 5.49 (s, 2H), 5.30 (s, 2H); 3.50 (t, J=6.0 Hz, 2H); 2.92 (t, J=6.0 Hz, 2H); 2.36 (s, 3H). ES-HRMS m/nz 543.0453 (M+H calcd for C₂₂H₂₂Br₂F₂N₂O₅S requires 543.0395).

Example 631

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxy-2-methylpropyl)benzenesulfonamide

Step 1: Preparation of 4-Bromomethyl-N-(2-hydroxy-2-methylpropyl)benzenesulfonamide

4-(Bromomethyl)benzenesulfonyl chloride (2.0 g, 7.3 mmol) was dissolved in tetrahydrofuran. 3-Amino-2-methyl-2-propanol (1.0 g, 8 mmol) and and N,N-diisopropylethylamine (1.5 mL, 8.8 mmol) were added, and the reaction was allowed to stir at ambient temperature for 30 minutes. The reaction was concentrated to an oil that was partitioned between water and ethyl acetate and extracted with ethyl acetate. The organic extracts were combined, washed with brine, dried over Na₂SO₄, and filtered. The resulting filtrate was concentrated to an oil that was a mixture of the title compound and 4-chloromethyl-N-(2-hydroxy-2-methylpropyl)benzenesulfonamide. The resulting oil was dried in vacuo (1.9 g, 81%).

Step 2: Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxy-2-methylpropyl)benzenesulfonamide. The title compound was prepared essentially according to the procedure described in Step 2 of Example 629, using 4-Bromomethyl-N-(2-hydroxy-2-methylpropyl)benzenesulfonamide (from step 1). ¹H NMR (400 MHz, CDCl₃) δ 7.78 (d, J=8.4 Hz, 2H); 7.56 (app q, J=7.6 Hz, 1H); 7.26 (d, J=8.4 Hz); 6.95 (app t, J=8.4 Hz, 1H), 6.86-6.83 (m, 1H); 6.07 (s, 1H), 5.41 (s, 2H), 5.22 (s, 2H); 4.98 (t, J=6.4 Hz, 1H); 2.84 (d, J=6.4 Hz, 2H); 2.29 (s, 3H); 1.21 (s, 6H). ES-HRMS m/z 571.0684 (M+H calcd for C₂₄H₂₆Br₂F₂N₂O₅S requires 571.0708).

Example 632

3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(1H-pyrazol-3-ylmethyl)-1H-pyridin-2-one

Step 1. Preparation of 4-hydroxy-6-methyl-1H-pyridin-2-one

4-Hydroxy-6-methyl-pryan-2-one (25.8 g, 0.2 mol) was dissolved in 180 ml of concentrated ammonium hydroxide. The reaction was heated at refluxed for 4 hours. The reaction was cooled to room temperature and evaporated on a rotary evaporator to a quarter of the original volume. The resulting solid was filtered, washed with cold water, hexanes, and dried in a vacuum oven overnight to give a white solid (25 g, 98%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.94 (br s, 1H), 10.34 (s, 1H), 5.59 (d, J=1.4 Hz, 1H), 5.32 (d, J=2.0 Hz, 1H), 2.07 (s, 3H).

Step 2. Preparation of 3-Chloro-4-hydroxy-6-methyl-1H-pyridin-2-one

4-Hydroxy-6-methyl-1H-pyridin-2-one (25 g, 0.2 mol) and N-chlorosuccinimide (29.4 g, 0.22 mol) were dissolved in 200 mL of acetic acid. The reaction was heated at 115° C. for 6 hours. The reaction was cooled to room temperature, the solid was filtered, and washed with acetic acid and hexanes. The solid was dried in a vacuum oven overnight to give a white solid (19.2 g, 60%): ¹H NMR (300 MHz, DMSO-d₆) δ 11.46 (br s, 1H), 11.04 (s, 1H), 5.79 (s, 1H), 2.09 (s, 3H).

Step 3. Preparation of 3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1H-pyridin-2-one

3-Chloro-4-hydroxy-6-methyl-1H-pyridin-2-one (19.2 g, 0.12 mol) and DBU (19.9 mL, 0.13 mol) were dissolved in 70 m]L of NMP. 2,4-Difluorobenzylbromide (17 mL, 0.13 mol) was added dropwise and the reaction was heated at 80° C. for 6 hours. The reaction was cooled to room temperature, the solid was filtered, and washed with NMP and hexanes. The solid was dried in a vacuum oven overnight to give a white solid (4.4 g, 13%): ¹H NMR (300 MHz, DMSO-d₆) δ 11.88 (br s, 1H), 7.63 (app q, J=9 Hz, 1H), 7.33 (app t, J=10 Hz, 1H), 7.16 (app t, J=9 Hz, 1H), 6.37 (s, 1H), 5.24 (s, 2H), 2.20 (s, 3H).

Step 4. Preparation of 3-Methylpyrazole-1-carboxylic Acid Tert-Butyl Ester

3-Methyl-1H-pyrazole (5.3 g, 65 mmol), DMAP (0.79 g, 6.5 mmol), and di-tert-butyl dicarbonate (2.8 g, 13 mmol) were at room temperature in 90 mL of CH₃CN for 1 hour. The reaction was evaporated on a rotary evaporator, and the resulting solid dissolved in EtOAc, washed with 1 N HCl, water and brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator to give a light yellow oil (11.4 g, 96%): ¹H NMR (300 MHz, CDCl₃) δ 7.96 (d, J=2.7 Hz, 1H), 6.17 (d, J=2.7 Hz, 1H), 2.32 (s, 3H), 1.63 (s, 9H).

Step 5. Preparation of 3-Bromomethylpyrazole-1-carboxylic Acid Tert-Butyl Ester

3-Methylpyrazole-1-carboxylic acid tert-butyl ester (6.0 g, 33 mmol), N-bromosuccinimide (1.0 g, 5.6 mmol) and benzoyl peroxide (50 mg) were dissolved in 20 mL of carbon tetrachloride. The reaction was heated at reflux for 16 h. The reaction was cooled to room temperature, filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:4 EtOAc/hexanes) gave a light yellow oil (4.5 g, 53%): ¹H NMR (300 MHz, CDCl₃) δ 8.03 (d, J=2.6 Hz, 1H), 6.47 (d, J=2.6 Hz, 1H), 4.48 (s, 2H), 1.64 (s, 9H).

Step 6. Preparation of 3-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]pyrazole-1-carboxylic Acid Tert-Butyl Ester

3-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]pyrazole-1-carboxylic acid tert-butyl ester was prepared by a procedure similar to the one described for Example 401 gave a yellow solid (1.4 g, 39%): ¹H NMR (300 MHz, CDCl₃) δ 7.53-7.49 (m, 2H), 6.97-6.81 (m, 2H), 6.35 (d, J=2.0 Hz, 1H), 6.01 (s, 1H), 5.32 (s, 2H), 5.26 (s, 2H), 2.52 (s, 3H), 1.62 (s, 9H).

Step 7. Preparation of the title compound Example 632 3-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]pyrazole-1-carboxylic acid tert-butyl ester (0.16 g, 0.34 mmol) was heated to 140° C. for 16 h. The reaction mixture was cooled to room temperature. Recrystallization from methylene chloride/hexanes provided an off-white solid (1.0 g, 91%): ¹H NMR (300 MHz, DMSO-d₆) δ 12.67 (br s, 1H), 7.67-7.60 (m, 2H), 7.34 (dt, J=10.5, 2.5 Hz, 1H), 7.17 (dt, J=8.5, 1.6 Hz, 1H), 6.52 (s, 1H), 6.10 (d, J=1.9 Hz, 1H), 5.27 (s, 2H), 5.20 (s, 2H), 2.48 (s, 2H).

Example 633

3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(2,3-dihydro-1H-indol-5-ylmethyl)-1H-pyridin-2-one

Step 1. Preparation of 5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]indole-1-carbamic Acid Tert-Butyl Ester

5-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-2H-pyridin-1-ylmethyl]indole-1-carbamic acid tert-butyl ester was prepared by a procedure similar to the one described for Example 632 as an off-white solid (2.5 g, 61%): ¹H NMR (300 MHz, DMSO-d₆) δ 8.00 (d, J=8.5 Hz, 1H), 7.70-7.62 (m, 2H), 7.39-7.32 (m, 2H), 7.21-7.13 (m, 2H), 6.70 (d, J=3.8 Hz, 1H), 6.66 (s, 1H), 5.40 (s, 2H), 5.29 (s, 2H), 2.33 (s, 3H), 1.62 (s, 9H).

Step 2. Preparation of 3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(1H-indol-5-ylmethyl)-1H-pyridin-2-one

5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]indole-1-carbamic acid tert-butyl ester (1.08 g, 2.1 mmol) dissolved in 40 mL of DMSO was stirred at 120° C. for 20 hours. The reaction was cooled to room temperature, diluted with water, and washed 5 times with ethyl acetate. The combined organics were washed 1 time with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. ¹H NMR (300 MHz, DMSO-d₆) δ 11.1 (br s, 1H), 7.67 (d, J=6.7 Hz, 1H), 7.36-7.32 (m, 2H), 7.23 (s, 1H), 7.18 (d, J=2.3 Hz, 1H), 6.93 (dd, J=8.4, 1.2 Hz, 1H), 6.57 (s, 1H), 6.38 (s, 1H), 5.37 (s, 2H), 5.29 (s, 2H), 2.35 (s, 3H).

Step 3. 3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(1H-indol-5-ylmethyl)-1H-pyridin-2-one (from Step 2) (1.7 g, 4.1 mmol) was stirred in 26 mL of acetic acid and NaCNBH₃ (0.27 g, 4.3 mmol) was added portionwise. The reaction was stirred for 1 hour. The reaction was diluted water, and washed 5 times with ethyl acetate. The combined organics were washed 1 time with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 100% EtOAc) gave a white solid (1.2 g, 71%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.64 (app q, J=8.5 Hz, 1H), 7.34 (dt, J=9.5, 2.6 Hz, 1H), 7.17 (app t, J=8.5, 1H), 6.82 (s, 1H), 6.72 (d, J=8.0 Hz, 1H), 6.53 (s, 1H), 6.42 (d, J=8.0 Hz, 1H), 5.48 (br s, 1H), 5.27 (s, 2H), 5.13 (s, 2H), 3.37 (t, J=8.3 Hz, 2H), 2.82 (t, J=8.3 Hz, 2H), 2.35 (s, 3H).

Example 634

5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-1,3-dihydro-indol-2-one

Step 1. Preparation of 5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-3,3-dibromo-1H-indol-2-one

3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(I H-indol-5-ylmethyl)-1H-pyridin-2-one (0.45 mg, 1.1 mmol)(example 633, step 2) was suspended in 11 mL of tert-butanol and pyridinium bromide perbromide (1.04 g, 3.3 mmol) was added portionwise. The reaction was stirred for 16 hours. The reaction was diluted with water, and washed 4 times with ethyl acetate. The combined organics were washed 1 time with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Trituration with methylene chloride gave an off-white solid (0.25 g, 39%): ¹H NMR (300 MHz, DMSO-dr) δ 11.26 (br s, 1H), 7.66 (app q, J=8.6 Hz, 1H), 7.48 (s, 1H), 7.35 (dt, J=10.5, 2.5 Hz, 1H), 7.18 (dt, J=8.7, 1.9, 1H), 7.05 (dd, J=8.2, 1.5, 1H), 6.88 (d, J=8.1 Hz, 1H), 6.61 (s, 1H), 5.29 (s, 4H), 2.36 (s, 3H).

Step 2. 5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-3,3-dibromo-1H-indol-2-one (0.2 g, 0.34 mmol) was suspended in 5 mL of acetic acid, and zinc metal (0.22 g, 3.4 mmol) was added. The reaction was stirred for 48 hours. The reaction was diluted with water, and washed 2 times with ethyl acetate. The combined organics were washed 1 time with brine, dried (MgSO₄), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 100% EtOAc) gave a white solid (0.12 g, 82%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.37 (br s, 1H), 7.65 (app q, J=6.9 Hz, 1H), 7.34 (dt, J=8.2, 2.5 Hz, 1H), 7.18 (dt, J=7.1, 1.9, 1H), 6.98 (br s, 2H), 6.77 (d, J=8.4 Hz, 1H), 6.57 (s, 1H), 5.28 (s, 2H), 5.23 (s, 2H), 3.44 (s, 2H), 2.34 (s, 3H).

Example 635

N-[(5-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-N-methylmethanesulfonamide

To a suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(methylamino)methyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one (0.16 g, 0.34 mmol) in acetonitrile at 0° C. was added triethylamine (0.043 g, 0.42 mmol), followed by the addition of methane sulfonylchloride (0.047 g, 0.41 mmol) and stirred at room temperature for 1 h under argon atmosphere. The solvents were removed in vacuo and the residue was triturated with water and filtered. It was washed with water an, acetonitrile and dried in vacuo to afford 0.11 g of material. ¹H NMR (CD₃OD/400 MHz) δ 8.62 (s, 1H), 8.55 (s, 1H), 7.61 (m, 1H), 7.0 (m, 2H), 6.53 (s, 1H), 5.47 (s, 2H), 5.29 (s, 2H), 4.49 (s, 2H), 2.95 (s, 3H), 2.85 (s, 3H), and 2.55 (s, 3H); ¹⁹F NMR(CD₃OD/400 MHz) δ −111.70 (m) and −116.07 (m); ES-HRMS m/z 543.0515 (M+H calcd for C₂₁H₂₂BrF₂N₄O₄S requires 543.0508).

Example 636

Methyl (5-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl(methyl)carbamate

To a cold (5° C.) solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(methylamino)methyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one (0.20 g, 0.4 mmol) in DMF (2.0 ml), was added methylchloroformate (0.049 g, 0.52 mmol), followed by the addition of triethylamine (0.072 g, 0.71 mmol). The mixture was stirred at 5° C. for 30 min and at room temperature for an additional 30 min and concentrated in vacuo. The residue was partitioned between water (5.0 mL) and EtOAc (10.0 mL). The organic extract was washed with water, dried (Na₂SO₄), and concentrated to dryness. The resulting material was purified by reverse-phase HPLC using 10-90% CH₃CN/Water gradient (60 min) at a flow rate of 70 mL/min. The appropriate fractions (m/z=523 M+H) were combined and freeze dried to give a white powder. This was partitioned between 5% NaHCO₃ (10 mL) and EtOAc (15 mL). The organic layer was washed with water, dried (Na₂SO₄), and concentrated to dryness to afford the title compound (0.12 g, 53%) as a white powder: ¹H NMR (CD₃OD/400 MHz) δ 8.59 (s, 1H), 8.41 (m, 1H), 7.60 (m, 1H), 7.05 (m, 2H), 6.52 (s, 1H), 5.45 (s, 2H), 5.29 (s, 2H), 4.58 (s, 2H), 3.69 and 3.64 (s, 3H), 2.97 (s, 3H), 2.85 (s, 3H), and 2.55 (s, 3H); ¹⁹F NMR(CD₃OD/400 MHz) 6-111.69 (m) and −116.09 (m); ES-HRMS m/z 523.0775 (M+H calcd for C₂₂H₂₂BrF₂N₄O₄ requires 523.0787).

Example 637

N-[(5-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-hydroxy-N,2-dimethylpropanamide

To a cold (5° C.) solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-({5-[(methylamino)methyl]pyrazin-2-yl}methyl)pyridin-2(1H)-one (0.24 g, 0.52 mmol) in DMF (2.0 ml), was added 2-acetoxyisobutyryl chloride (0.093 g, 0.56 mmol), followed by the addition of triethylamine (0.072 g, 0.71 mmol). The mixture was stirred at room temperature for an additional 2 h and concentrated in vacuo. The residue was partitioned between water (5.0 mL) and EtOAc (15.0 mL). The EtOAc extract was washed with water, dried (Na₂SO₄), and concentrated to dryness. The resulting material (0.2 g) was stirred with 1M. LiOH (0.5 mL, MeOH/Water 1:1 v/v) at room temperature for 3 h, cooled, acidified with trifluoroacetic acid and the product was purified by reverse-phase HPLC using 10-90% CH₃CN/Water gradient (60 min) at a flow rate of 70 mL/min. The appropriate fractions (m/z=551 M+H) were combined and freeze dried to give a white powder. This was partitioned between 5% NaHCO₃ (10 mL) and EtoAc (15 mL). The organic layer was washed with water, dried (Na₂SO₄), and concentrated to dryness to afford the title compound (0.075 g) as a white powder: ¹H NMR (CD₃OD/400 MHz) δ 8.59 (s, 1H), 8.41 (br, 1H), 7.60 (m, 2H), 7.01 (m, 2H), 6.52 (s, 1H), 5.45 (s, 2 h), 5.29 (s, 2H).

Example 638

5-{[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxy-2-methylpropyl)pyrazine-2-carboxamide

To a solution of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylic acid (0.42 g, 0.9 mmol) in DMF (3.0 mL) was added isobutylchloroformate (0.126 g, 0.13 mmol) followed by the addition of N-methylmorpholine (0.11 g, 1.1 mmol) and stirred at −10° C., under argon atmosphere. After 20 min, added a solution of 1,1 dimethyl-2-aminoethanol hydrochloride (0.135 g, 1.1 mmol) in DMF (2.0 mL) containing N-methylmorpholine (0.11 g, 1.1 mmol). The mixture was stirred at room temperature for 1 h, and concentrated to dryness in vacuo. The resulting residue was purified by reverse-phase HPLC using 10-90% CH₃CN/Water gradient (60 min) at a flow rate of 70 mL/min. The appropriate fractions (m/z=537 M+H) were combined and freeze dried to give a white powder. This was partitioned between 5% NaHCO₃ (10 mL) and EtOAc (15 mL). The organic layer was washed with water, dried (Na₂SO₄), and concentrated to dryness to afford the title compound (0.35 g, 75%) as a white powder: ¹H NMR (CD₃OD/400 MHz) δ 9.1 (d, 1H, J=1.6 Hz), 8.71 (d, 1H, J=1.6 Hz), 7.61 (m 1H), 7.02 (m, 2H), 6.54 (s, 1H), 5.54 (s, 2H), 5.30 (s, 2 h). 3.30 (s, 2 h), 2.55 (s, 3H), and 1.21 (s, 6H); ¹⁹F NMR(CD₃OD/400 MHz) δ −111.67 (m) and −116.05 (m); ES-HRMS m/z 537.0948 (M+H calcd for C₂₃H₂₄BrF₂N₄O₄ requires 537.0943).

Example 639

1-[(5-Aminopyrazin-2-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Trifluoroacetate

A mixture of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazine-2-carboxylic acid (0.70 g, 1.5 mmol) diphenylphosphoryl azide (0.51 g, 1.8 mmol) in dimethylacetamide (15.0 mL) and t-butanol (5.0 mL) containing triethylamine (0.18 g, 1.8 mmol) was heated at 90° C. for 6 h under argon atmosphere. The reaction mixture was cooled, filtered the precipitate. It was washed with acetonitrile and dried to obtain 0.22 g of the unreacted acid. The combilned filtrate and the washings were concentrated in vacuo and the resulting material was purified by reverse-phase HPLC using 10-90% CH₃CN/Water gradient (60 min) at a flow rate of 70 ml/min. The appropriate fractions (m/z=437 M+H) were combined and freeze dried to give the title compound (0.21 g, 37%) as a white powder: ¹H NMR (DMSO-d₆/400 MHz) δ 7.88 (d, 1H, J=1.2 Hz), 7.75 (d, 1H, J=1.2 Hz), 7.61 (m 1H), 7.34 (m, 1H), 7.18 (m, 1H), 6.49 (s, 1H), 5.25 (s, 2H), 5.10 (s, 2H), and 2.49 (s, 3H); ¹⁹F NMR(CD₃OD/400 MHz) δ −111.72 (m) and −116.11 (m); ES-HRMS m/z 437.0402 (M+H calcd for C₁₈H₁₆BrF₂N₄O₂ requires 437.0419).

Example 640

3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(3-methyl-1,2,4-triazin-6-yl)methyl]pyridin-2(1H)-one Trifluoroacetate

Step 1: Preparation of (2-methylpyrimidin-5-yl)methanol Trifluoroacetate

To solution of methyl 2-methylpyrimidinecarboxylate (2.6 g, 17.1 mmol) in THF was added dropwise diisobutylaluminumhydride (39.5 mL, 1M solution in THF) and stirred at −20° C. under argon atmosphere for 1.5 h, and at room temperature for 2 h. The reaction was quenched by the addition of powdered sodiumsulphate decahydrate (25 g), added THF (25 mL) and stirred at room temperature for 1 h. This mixture was allowed to stand in the refrigerator overnight and filtered through a celite pad. The precipitate was thoroughly with warm THF (100 mL) containing 10% ethanol. The combined washings and the filtrate were concentrated to afford a yellow syrup, which was purified by reverse-phase HPLC using 10-90% CH₃CN/Water gradient (60 min) at a flow rate of 70 ml/min. The appropriate fractions (m/z=125 M+H) were combined and lyophilized to give the title compound (0.67 g, 32%) as its trifluoroacetate salt: ¹H NMR (CD₃OD/400 MHz) δ 8.65 (s, 2H) 4.62 (s, 2H), and 2.66 (s, 3H); ES-HRMS m/z 125.0678 (M+H calcd for C₆H₉N₂O requires 125.0709).

Step 2: Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(3-methyl-1,2,4-triazin-6-yl)methyl]pyridin-2(1H)-one Trifluoroacetate

To a solution of (2-methylpyrimidin-5-yl)methanol trifluoroacetate (0.9 g, 3.76 mmol) in dichloromethane (10 mL) at 0° C., was added triethylamine (0.95 g, 9.41 mmol), followed by the addition of methanesulfonyl chloride (0.59 g, 5.17 mmol) and stirred at 0° C. for 1 h. After stirring for 1 h at room temperature, additional triethylamine (0.22 g) and methanesulfonyl chloride (0.15 g) were added and the mixture was stirred at room temperature for another hour under argon atmosphere. The reaction was quenched by the addition of cold water (15 mL) and stirred for 15 min. The organic layer was washed with water, followed by 5% sod. bicarbonate (2×15 mL), water, and dried (Na₂SO₄). After the removal of the solvent under reduced pressure, the residue was dried in a desiccator under vacuum for 4 h. This material was suspended in THF (10 mL) and DMF (5.0 mL), added 3-bromo-4-(2,4-difluorophenoxy)-6-methylpyridin-2(1H)-one (0.5 g, 1.52 mmol) and NaH (0.04 g). The resulting mixture was heated at 65° C. for 16 h under argon atmosphere. The solvents were distilled under vacuum and the residue was purified by reverse-phase HPLC using 10-90% CH₃CN/Water gradient (60 min) at a flow rate of 70 ml/min. The appropriate fractions (m/z=436 M+H) were combined and freeze dried to give the title compound (0.045 g,) as its trifluoroacetate salt: ¹H NMR (CD₃OD/400 MHz) δ 8.58 (s, 2H) 7.61 (m, 1H), 7.01 (m, 2H), 6.53 (s, 1H), 5.37 (s, 2 h), 5.29 (s, 2H), 2.65 (s, 3H), and 2.46 (s, 3H); ¹⁹F NMR(CD₃OD/400 MHz) δ −111.62 (m), and −116.08 (m); ES-HRMS m/z 436.0433 (M+H calcd for C₁₉H₁₇BrF₂N₃O₂ requires 436.0467).

Example 641

3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-(1H-indazol-5-yl)-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-hydroxy-1-(1H-indazol-5-yl)-6-methylpyridin-2(1H)-one

A mixture of 4-hydoxy-6-methyl-2-pyrone (3.75 g, 0.029 mol) and 5-aminoindazole (4.0 g, 0.03 mol) in water (70 ml) was heated at 90° C. under argon for 1 h. The mixture was cooled, decanted the supernatant and residue was triturated with ethanol, cooled and filtered the solid. It was washed with cold ethanol, and dried. ¹H NMR (CD₃OD/400 MHz) δ 8.11 (s, 1H), 7.64 (m, 2H), 7.18 (d, 1H, J=2.0 Hz), 7.16 (d, 1H, J=2.0 Hz) 6.07 (m, 1H), 5.81 (d, 1H, J=2.8 Hz), and 1.94 (s, 3H); ES-HRMS m/z 242.0962(M+H calcd for C₁₃H₁₂N₃O₂ requires 242.0924).

Step 2: A mixture of 4-hydroxy-1-(1H-indazol-5-yl)-6-methylpyridin-2(1H)-one (0.2 g, 0.83 mmol), N-bromosuccinmide (0.15 g, 0.84 mmol) in dichloromethane (4.0 mL) and acetic acid (1.0 mL) was stirred at room temperature under argon atmosphere for 2.5 h. After the removal of the solvents, the residue was dried in vacuo for 4 h in a desiccator. It was then suspended in DMF (3.0 mL), potassium carbonate (0.1 g), and 2,4 difluorobenzyl bromide were added and mixture was stirred at room temperature for 3 h. DMF was distilled in vacuo and the residue was purified by reverse-phase HPLC using 10-90% CH₃CN/Water gradient (60 min) at a flow rate of 70 ml/min. The appropriate fractions (m/z=537 M+H) were combined and freeze dried to give a white powder. This was partitioned between 5% NaHCO₃ (10 mL) and EtOAc (15 mL). The organic layer was washed with water, dried (Na₂SO₄), and concentrated to dryness to afford the title compound (0.075 g) as a white powder: ¹H NMR (CD₃OD/400 MHz) δ 8.13 (s, 1H), 7.68 (m, 3H), 7.20 (2d, 1H, J=1.2 Hz), 7.05 (m, 2H), 6.61 (s, 1H), 5.35 (s, 2H), and 2.05 (s, 3H); ¹⁹F NMR(CD₃OD/400 MHz) −111.62 (m) and −116.02 (m); ES-HRMS m/z 446.0305 (M+H calcd for C₂₀H₁₅BrF₂N₃O₂ requires 446.0310).

Example 642

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(1H-indazol-6-yl)-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-hydroxy-1-(H-indazol-6-yl)-6-methylpyridin-2(1H)-one

The title compound was prepared by a similar procedure described for 4-hydroxy-1-(1H-indazol-5-yl)-6-methylpyridin-2(1H)-one. Yield=12%; ¹H NMR (CD₃OD/400 MHz) δ 8.12 (s, 1H), 7.90 (d, 1H, J=8.0 Hz), 7.42 (s, 1H), 6.94 (d, 1H, J=8.8 Hz) 6.08 (br s, 1H), 5.81 (d, 1H, J=2.4 Hz), and 1.96 (s, 3H); ES-HRMS m/z 242.0946(M+H calcd for C₁₃H₁₂N₃O₂ requires 242.0924).

Step 2:

The title was prepared by a similar procedure described for 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-(1H-indazol-5-yl)-6-methylpyridin-2(1H)-one. ¹H NMR (CD₃OD/400 MHz) δ 8.14 (s, 1H), 7.93 (d, 1H, J=8.4 Hz), 7.61 (m 1H), 7.46 (s, 1H), 7.04 (m, 2H), 6.98 (m, 1H) 6.62 (s, 1H), 5.36 (s, 2H), and 2.06 (s, 3H); ¹⁹F NMR(CD₃OD/400 MHz) −111.62 (m) and −116.03 (m); ES-HRMS m/z 446.0302 (M+H calcd for C₁₃H₁₂N₃O₂ requires 446.0310).

Example 643

Methyl 2-{[(3-bromo-6-methyl-1-{2-methyl-5-[(methylamino)carbonyl]phenyl}-2-oxo-1,2-dihydropyridin-4-yloxy]methyl}-5-fluorobenzylcarbamate

Step 1: Preparation of methyl 3-[4-[(2-cyano-4-fluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

To a cooled (0° C.) solution of 2-(bromomethyl)-5-fluorobenzonitrile (4.31 g, 20.1 mmol) and methyl 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-methylbenzoate (5.00 g, 18.3 mmol) in DMF (20 mL) was added K₂CO₃ (3.00 g, 22.0 mmol). The reaction was allowed to warm to RT and stirred overnight. Additional 2-(bromomethyl)-5-fluorobenzonitrile (0.39 g, 1.83 mmol) and K₂CO₃ (0.25 g, 1.83 mmol) were added and the reaction heated at 60° C. for 2 h. Solvent removed by distillation. Reaction neutralized with 5% citric acid (50 mL). Organic products were extracted in DCM (3×25 mL), dried over Na₂SO₄, filtered, and concentrated to a thick dark brown oil. Purified by silica gel flash column chromatography using EtOAc as the eluent to give the product as a brown solid, dried in vacuo (6.18 g, 76%). ¹H NMR (CD₃OD/400 MHz) δ 8.03 (m, 1H), 7.76 (m, 2H), 7.66 (m, 1H), 7.52 (m, 2H), 6.24 (s, 1H), 6.09 (s, 1H), 5.27 (s, 2H), 3.89 (s, 3H), 2.12 (s, 3H), 1.90 (s, 3H). ESHRMS m/z 407.1408 (M+H calculated for C₂₃H₂₀FN₂O₄ requires 407.1402).

Step 2: Preparation of Methyl 3-[4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate Trifluoroacetate

To a cooled (0° C.) solution of methyl 3-[4-[(2-cyano-4-fluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (from Step 1) (0.510 g, 1.25 mmol) in THF (5 mL) was added dropwise BH₃THF (2.51 mL, 2.51 mmol). The reaction was then stirred at RT for 2.5 h. Reaction cooled (0° C.), quenched by the slow addition of MeOH, concentrated, and purified by preparatory HPLC. The product was isolated by freeze-drying and evaporation of the solvent to give a white solid, dried in vacuo (0.39 g, 76%). ¹H NMR (CD₃OD/400 MHz) 68.04 (m, 1H), 7.75 (s, 1H), 7.63 (m, 1H), 7.55 (d, 1H, J=8.4 Hz), 7.32 (m, 1H), 7.24 (m, 1H), 6.25 (s, 1H), 6.12 (s, 1H), 5.23 (s, 2H), 4.25 (s, 2H), 3.90 (s, 3H), 2.11 (s, 3H), 1.90 (s, 3H). ESHRMS m/z 411.1691 (M+H calculated for C₂₃H₂₄FN₂O₄ requires 411.1715).

Step 3: Preparation of Methyl 3-[4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

To a cooled (0° C.) solution of methyl 3-[4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate trifluoroacetate (from Step 2) (0.50 g, 0.95 mmol) in DMA (4 mL) was added 4-methylmorpholine (0.21 mL, 1.9 mmol) and methyl chloroformate (0.08 mL, 1.0 mmol). Reaction was stirred at RT for 1 h. Solvent removed by distillation. Crude product purified by preparatory HPLC. Acetonitrile was evaporated and the solution washed with 5% NaHCO₃ (30 mL) and extracted in DCM (3×25 mL). The organic extracts were dried over Na₂SO₄, filtered, and concentrated to a white solid, dried in vacuo (0.36 g, 81%). ¹H NMR (CD₃OD/400 MHz) 68.03 (m, 1H), 7.77 (s, 1H), 7.53 (d, 1H, J=7.6 Hz), 7.47 (m, 1H), 7.12 (m, 1H), 7.03 (m, 1H), 6.21 (s, 1H), 6.08 (s, 1H), 5.18 (s, 2H), 4.38 (s, 2H), 3.89 (s, 3H), 3.65 (s, 3H), 2.12 (s, 3H), 1.89 (s, 3H). ESHRMS m/z 469.1767 (M+H calculated for C₂₅H₂₆FN₂O₆ requires 469.1769).

Step 4: Preparation of 3-[4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

To methyl 3-[4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (from Step 3) (0.17 g, 0.36 mmol) was added 1.5 N NaOH solution in 1:1 MeOH:water (0.39 mL, 0.59 mmol). The reaction mixture was stirred at 60° C. for 2.5 h. The solution was cooled (0° C.), neutralized by the slow addition of 5% citric acid, and organic products extracted in DCM. A white solid suspended in the organic layer was filtered, washed with DCM and water, dried in vacuo, and found to be the desired product (0.090 g, 55%). ¹H NMR (CD₃OD/400 MHz) δ 8.03 (m, 1H), 7.75 (s, 1H), 7.52 (d, 1H, J=8.0 Hz), 7.47 (m, 1H), 7.12 (m, 1H), 7.03 (m, 1H), 6.21 (s, 1H), 6.08 (s, 1H), 5.18 (s, 2H), 4.38 (s, 2H), 3.65 (s, 3H), 2.12 (s, 3H), 1.90 (s, 3H). ESHRMS m/z 455.1632 (M+H calculated for C₂₄H₂₄FN₂O₆ requires 455.1613).

Step 5: Preparation of 3-[3-bromo-4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

NBS (0.69 g, 3.85 mmol) was added to a solution of 3-[4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (from Step 4) (1.75 g, 3.85 mmol) in DCM (45 mL). After 1.5 h, solvent removed on rotary evaporator. Solid dissolved in EtOAc and hexane added, resulting in a solid precipitate. Solid filtered. Solid subsequently dissolved in DCM and washed with water. Organic layer dried over Na₂SO₄, filtered, and concentrated. Pale yellow solid dried in vacuo (1.47 g, 72%). ¹H NMR (CD₃OD/400 MHz) 88.04 (m, 1H), 7.77 (s, 1H), 7.54 (m, 2H), 7.13 (m, 1H), 7.05 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.44 (s, 2H), 3.64 (s, 3H), 2.09 (s, 3H), 1.99 (s, 3H). ESHRMS m/z 533.0700 and 535.0677 (M+H calculated for C₂₄H₂₃BrFN₂O₆ requires 533.0718 and 535.0701).

Step 6: Preparation of the Title Compound

To a cooled (−10° C.) solution of 3-[3-bromo-4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (0.07 g, 0.13 mmol) in DMF (2.0 mL) was added isobutyl chloroformate (0.02 mL, 0.16 mmol) and 4-methylmorpholine (0.02 mL, 0.16 mmol). After 15 min, 2.0M methylamine in THF (0.01 mL, 0.20 mmol) was added. Solvent removed by distillation after 30 min. Crude product purified by preparatory HPLC. Acetonitrile was evaporated and the solution washed with 5% NaHCO₃ (30 mL) and extracted in DCM (3×25 mL). The organic extracts were dried over Na₂SO₄, filtered, concentrated, and dried in vacuo to give a white foam, (0.061 g, 86%). ¹H NMR (CD₃OD/400 MHz) δ 7.85 (m, 1H), 7.54 (m, 3H), 7.14 (m, 1H), 7.05 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.43 (s, 2H), 3.64 (s, 3H), 2.89 (s, 3H), 2.08 (s, 3H), 1.99 (s, 3H). ESHRMS m/z 546.0987 and 548.1018 (M+H calculated for C₂₅H₂₆BrFN₃O₅ requires 546.1034 and 548.1018).

Example 644

Methyl 2-({[3-bromo-1-(5-{[(2-hydroxyethyl)amino]carbonyl}-2-methylphenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

The title compound was prepared using a procedure similar to that used in the preparation of Example 643. ¹H NMR (CD₃OD/400 MHz) δ 7.88 (m, 1H), 7.61 (s, 1H), 7.53 (m, 2H), 7.13 (m, 1H), 7.04 (m, 1H), 6.68 (s, 1H), 5.41 (s, 2H), 4.43 (s, 2H), 3.68 (t, 2H, J=5.6 Hz), 3.64 (s, 3H), 3.48 (t, 2H, J=5.6 Hz), 2.08 (s, 3H), 2.00 (s, 3H). ESHRMS m/z 576.1101 and 578.1072 (M+H calculated for C₂₆H₂₈BrFN₃O₆ requires 576.1140 and 578.1124).

Example 645

Methyl 2-({[3-bromo-1-(5-[(2-hydroxy-2-methylpropyl)amino]carbonyl 1-2-methylphenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

The title compound was prepared using a procedure similar to that used in the preparation of Example 643. ¹H NMR (CD₃OD/400 MHz) 87.89 (m, 1H), 7.63 (s, 1H), 7.54 (m, 2H), 7.13 (m, 1H), 7.04 (m, 1H), 6.69 (s, 1H), 5.41 (s, 2H), 4.43 (s, 2H), 3.64 (s, 3H), 3.38 (s, 2H), 2.09 (s, 3H), 2.01 (d, 6H, J=3.2 Hz), 1.21 (s, 3H). ESHRMS m/z 604.1412 and 606.1418 (M+H calculated for C₂₈H₃₂BrFN₃O₆ requires 604.1453 and 606.1438).

Example 646

Methyl 2-({[3-bromo-1-(5-{[(2-methoxyethyl)amino]carbonyl}-2-methylphenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

The title compound was prepared using a procedure similar to that used in the preparation of Example 643. ¹H NMR (CD₃OD/400 MHz) δ 7.87 (m, 1H), 7.59 (s, 1H), 7.53 (m, 2H), 7.14 (m, 1H), 7.05 (m, 1H), 6.68 (s, 1H), 5.41 (s, 2H), 4.44 (s, 2H), 3.64 (s, 3H), 3.54 (s, 4H), 3.35 (s, 3H), 2.08 (s, 3H), 2.00 (s, 3H). ESHRMS m/z 590.1267 and 592.1219 (M+H calculated for C₂₇H₃₀BrFN₃O₆ requires 590.1297 and 592.1281).

Example 647

Methyl 2-[({1-[5-(aminocarbonyl)-2-methylphenyl]-3-bromo-6-methyl-2-oxo-1,2-dihydropyridin-4-yl}oxy)methyl]-5-fluorobenzylcarbamate

The title compound was prepared using a procedure similar to that used in the preparation of Example 643. ¹H NMR (CD₃OD/400 MHz) δ 7.91 (m, 1H), 7.64 (s, 1H), 7.54 (m, 2H), 7.14 (m, 1H), 7.05 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.44 (s, 2H), 3.64 (s, 3H), 2.09 (s, 3H), 2.00 (s, 3H). ESHRMS m/z 532.0836 and 534.0787 (M+H calculated for C₂₄H₂₄BrFN₃O₅ requires 532.0878 and 534.0861).

Example 648

N-[2-({[3-chloro-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzyl]-N′-phenylurea

To a cooled (0° C.) solution of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-chloro-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate (0.25 g, 0.48 mmol) in DMA (2.0 mL) was added 4-methylmorpholine (0.06 mL, 0.53 mmol) and phenyl isocyanate (0.06 mL, 0.53 mmol). The reaction was stirred at RT for 1.5 h. Solvent distilled and crude product purified by preparatory HPLC. Acetonitrile was evaporated and the solution washed with 5% NaHCO₃ (30 mL) and extracted in DCM (3×25 mL). The organic extracts were dried over Na₂SO₄, filtered, and concentrated to a white solid, dried in vacuo (0.18 g, 71%). ¹H NMR (CD₃OD/400 MHz) δ 7.60 (m, 1H), 7.54 (m, 1H), 7.33 (d, 2H, J=7.6 Hz), 7.22 (m, SH), 7.06 (m, 1H), 6.95 (t, 1H, J=7.2 Hz), 6.73 (s, 1H), 5.44 (s, 2H), 4.53 (s, 2H), 2.07 (s, 3H). ESHRMS m/z 528.1304 (M+H calculated for C₂₇H₂₂ClF₃N₃O₃ requires 528.1296).

Example 649

Thien-3-ylmethyl 2-({[3-chloro-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

To a cooled (0° C.) solution of 4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-3-chloro-1-(2,6-difluorophenyl)-6-methylpyridin-2(1H)-one trifluoroacetate (0.26 g, 0.50 mmol) and 1, 1-carbonyldiimidazole (0.10 g, 0.60 mmol) in DMA (2.0 mL) was added 4-methylmorpholine (0.06 mL, 0.55 mmol). After 1 h at RT, 3-thiophenemethanol (0.09 mL, 0.99 mmol) was added. No product was observed after 2 h at RT. NaH (0.01 g, 0.50 mmol) was added and the reaction stirred at 60° C. Reaction was complete after 20 min. The reaction mixture was cooled (0° C.) and acetic acid added to quench the reaction. Solvent removed by distillation. Crude product purified by preparatory HPLC. Acetonitrile was evaporated and the solution washed with 5% NaHCO₃ (30 mL) and extracted in DCM (3×25 mL). The organic extracts were dried over Na₂SO₄, filtered, and concentrated to a white foam, dried in vacuo (0.20 g, 73%). ¹H NMR (CD₃OD/400 MHz) δ 7.61 (m, 1H), 7.52 (m, 1H), 7.34 (s, 2H), 7.23 (t, 3H, J=8.4 Hz), 7.10 (m, 2H), 6.71 (s, 1H), 5.40 (s, 2H), 5.07 (s, 2H), 4.43 (s, 2H), 2.10 (s, 3H). ESHRMS m/z 549.0858 (M+H calculated for C₂₆H₂₁ClF₃N₂O₄S requires 549.0857).

Example 650

Ethyl-2-{[(3-bromo-6-methyl-1-2-methyl-5-[(methylamino)carbonyl]phenyl 1-2-oxo-1,2-dihydropyridin-4-yl)oxy]methyl}-5-fluorobenzylcarbamate

Step 1: Preparation of Methyl 3-[4-[(2-{[(ethoxycarbonyl)amino]methyl}-4-fluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

Prepared using a procedure similar to that used in the preparation of methyl 3-[4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]4-methylbenzoate. ¹H NMR (CD₃OD/400 MHz) δ 8.03 (m, 1H), 7.76 (s, 1H), 7.53 (d, 1H, J=8.0 Hz), 7.47 (m, 1H), 7.12 (m, 1H), 7.03 (m, 1H), 6.21 (s, 1H), 6.08 (s, 1H), 5.18 (s, 2H), 4.38 (s, 2H), 4.08 (q, 2H, J=6.8 Hz), 3.89 (s, 3H), 2.12 (s, 3H), 1.89 (s, 3H), 1.23 (t, 3H, J=6.8 Hz). ESHRMS m/z 483.1900 (M+H calculated for C₂₆H₂₈FN₂O₆ requires 483.1926).

Step 2: Preparation of 3-[4-[(2-{[(ethoxycarbonyl)amino]methyl}-4-fluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

Prepared using a procedure similar to that used in the preparation of 3-[4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid. ¹H NMR (CD₃OD/400 MHz) δ 8.03 (m, 1H), 7.74 (s, 1H), 7.48 (m, 2H), 7.11 (m, 1H), 7.03 (m, 1H), 6.21 (s, 1H), 6.08 (s, 1H), 5.18 (s, 2H), 4.38 (s, 2H), 4.08 (q, 2H, J=7.2 Hz), 2.11 (s, 3H), 1.90 (s, 3H), 1.23 (t, 3H, J=7.2 Hz). ESHRMS m/z 469.1738 (M+H calculated for C₂₅H₂₆FN₂O₆ requires 469.1769).

Step 3: Preparation of 3-[3-bromo-4-[(2-{[(ethoxycarbonyl)amino]methyl}-4-fluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

Prepared using a procedure similar to that used in Step 5 of the synthesis of Example 643. ¹H NMR (CD₃OD/400 MHz) δ 8.04 (m, 1H), 7.76 (s, 1H), 7.55 (m, 2H), 7.13 (m, 1H), 7.05 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.43 (s, 2H), 4.07 (m, 2H), 2.09 (s, 3H), 1.99 (s, 3H), 1.22 (t, 3H, J=7.2 Hz). ESHRMS m/z 547.0842 and 549.0818 (M+H calculated for C₂₅H₂₅BrFN₂O₆ requires 547.0875 and 549.0858).

Step 4: ethyl-2-{[(3-bromo-6-methyl-1-{2-methyl-5-[(methylamino)carbonyl]phenyl}-2-oxo-1,2-dihydropyridin-4-yl)oxy]methyl}-5-fluorobenzylcarbamate. Prepared using a procedure similar to that used in the preparation of Example 643. ¹H NMR (CD₃OD/400 MHz) 67.85 (m, 1H), 7.54 (m, 3H), 7.13 (m, 1H), 7.04 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.43 (s, 2H), 4.07 (q, 2H), 2.89 (s, 3H), 2.08 (s, 3H), 1.99 (s, 3H), 1.23 (t, 3H, J=7.2 Hz). ESHRMS m/z 560.1215 and 562.1193 (M+H calculated for C₂₆H₂₈BrFN₃O₅ requires 560.1191 and 562.1175).

Example 651

3-[3-bromo-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

Step 1: Preparation of Methyl 3-[4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

To a cooled (0° C.) solution of methyl 3-[4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate trifluoroacetate (1.13 g, 2.16 mmol) and 1,1-carbonyldiimidazole (0.42 g, 2.59 mmol) in DMA (8.0 mL) was added 4-methylmorpholine (0.36 mL, 3.2 mmol). After 30 minutes at room temperature, the reaction was cooled to approximately 0° C. and an excess of cyclopropylamine was added. Reaction was stirred at RT for 2 h. DMA removed by distillation. Crude product purified by preparatory HPLC. Acetonitrile was evaporated and the solution washed with 5% NaHCO₃ (30 mL) and extracted in DCM (3×25 mL). The organic extracts were dried over Na₂SO₄, filtered, concentrated, and dried in vacuo (0.78 g, 73%). ¹H NMR (CD₃OD/400 MHz) δ 8.03 (m, 1H), 7.76 (s, 1H), 7.53 (d, 1H, J=8.0 Hz), 7.46 (m, 1H), 7.12 (m, 1H), 7.01 (m, 1H), 6.22 (s, 1H), 6.08 (s, 1H), 5.19 (s, 2H), 4.44 (s, 2H), 3.89 (s, 3H), 2.48 (m, 1H), 2.12 (s, 3H), 1.89 (s, 3H), 0.70 (m, 2H), 0.47 (m, 2H). ESHRMS m/z 494.2076 (M+H calculated for C₂₇H₂₉FN₃O₅ requires 494.2086).

Step 2: Preparation of 3-[4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

Prepared using a procedure similar to that used in the preparation of 3-[4-[(4-fluoro-2-{[(methoxycarbonyl)amino]methyl}benzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid. ¹H NMR (CD₃OD/400 MHz) δ 8.02 (m, 1H), 7.74 (s, 1H), 7.48 (m, 2H), 7.12 (m, 1H), 7.01 (m, 1H), 6.22 (s, 1H), 6.08 (s, 1H), 5.19 (s, 2H), 4.44 (s, 2H), 2.48 (m, 1H), 2.11 (s, 3H), 1.90 (s, 3H), 0.69 (m, 2H), 0.47 (m, 2H). ESHRMS m/z 480.1921 (M+H calculated for C₂₆H₂₇FN₃O₅ requires 480.1929).

Step 3: Preparation of 3-[3-bromo-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

Prepared using a procedure similar to that used in Step 5 of the synthesis of Example 643. ¹H NMR (DMSO-d₆/400 MHz) δ 7.92 (m, 1H), 7.67 (s, 1H), 7.54 (m, 2H), 7.12 (m, 2H), 6.71 (s, 1H), 5.37 (s, 2H), 4.31 (d, 2H, J=6.4 Hz), 2.40 (m, 1H), 2.00 (s, 3H), 1.88 (s, 3H), 0.56 (m, 2H), 0.33 (m, 2H). ESHRMS m/z 558.0988 and 560.0981 (M+H calculated for C₂₆H₂₆BrFN₃O₅ requires 558.1034 and 560.1018).

Step 4: 3-[3-bromo-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

Prepared using a procedure similar to that used in the preparation of Example 643. ¹H NMR (CD₃OD/400 MHz) δ 7.85 (m, 1H), 7.54 (m, 3H), 7.14 (m, 1H), 7.03 (m, 1H), 6.69 (s, 1H), 5.41 (s, 2H), 4.48 (s, 2H), 2.89 (s, 3H), 2.48 (m, 1H), 2.08 (s, 3H), 1.99 (s, 2H), 0.70 (m, 2H), 0.47 (m, 2H). ESHRMS m/z 571.1348 and 573.1355 (M+H calculated for C₂₇H₂₉BrFN₄O₄ requires 571.1351 and 573.1335).

Example 652

3-[3-bromo-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

Step 1: Preparation of Ethyl(5-fluoro-2-methylphenoxy)acetate

To a solution of 5-fluoro-2-methylphenol (1.00 g, 7.93 mmol) and ethylbromoacetate (1.59 g, 9.51 mmol) in DMF (15 mL) was added K₂CO₃ (1.10 g, 7.93 mmol). After 30 min at RT, DMF was removed by distillation. The crude product was washed with 5% citric acid (30 mL) and water (30 mL), extracted in DCM (3×20 mL), dried over Na₂SO₄, filtered, concentrated, and dried in vacuo. Desired product obtained as yellow oil (1.30 g, 77%). ¹H NMR (CD₃OD/400 MHz) δ 7.09 (t, 1H, J=8.8 Hz), 6.58 (m, 1H), 6.56 (m, 1H), 4.71 (s, 2H), 4.23 (q, 2H, J=7.2 Hz), 2.18 (s, 3H), 1.27 (t, 3H, J=7.2 Hz). ESHRMS m/z 212.0847 (M+H calculated for C₁₁H₁₃FO₃ requires 212.0849).

Step 2: Preparation of Ethyl [2-(bromomethyl)-5-fluorophenoxy]acetate

A solution of ethyl (5-fluoro-2-methylphenoxy)acetate (from Step 1) (0.65 g, 3.06 mmol), NBS (0.65 g, 3.68 mmol), and benzoyl peroxide (0.05 g, 0.21 mmol) in CCl4 (7.0 mL) were refluxed at 90° C. for 2.5 h. Additional NBS (0.16 g, 0.92 mmol) added, and reaction continued overnight. Solid filtered and filtrate concentrated onto silica gel. Purified by flash column chromatography using hexane and 2.5% EtOAc/hexane as eluent. Product obtained as yellow liquid (0.27 g, 30%). ¹H NMR (CD₃OD/400 MHz) 87.37 (m, 1H), 6.69 (m, 2H), 4.80 (s, 2H), 4.60 (s, 2H), 4.23 (q, 2H, J=7.2 Hz), 1.27 (t, 3H, J=7.2 Hz).

Step 3: Preparation of Ethyl [2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorophenoxy]acetate

To a solution of ethyl [2-(bromomethyl)-5-fluorophenoxy]acetate (from Step 2) (0.59 g, 2.03 mmol) and 3-bromo-1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (0.61 g, 1.93 mmol) in DMF (3.0 mL) was added K₂CO₃ (0.34 g, 2.43 mmol). After 2 h at RT, DMF was removed by distillation. The crude product was washed with 5% citric acid, extracted in DCM, dried over Na₂SO₄, filtered, and concentrated onto silica gel. Purified by flash column chromatography using 50% EtOAc/hexane as the eluent. Obtained product as a pale yellow solid (0.45 g, 42%). ¹H NMR (CD₃OD/400 MHz) δ 7.21 (q, 3H, J=8.4 Hz), 6.80 (m, 2H), 6.69 (s, 1H), 6.15 (s, 1H), 5.40 (s, 2H), 4.84 (s, 2H), 4.23 (q, 2H, J=6.8 Hz), 2.08 (s, 3H), 1.26 (t, 3H, J=6.8 Hz). ESHRMS m/z 526.0446 and 528.0414 (M+H calculated for C₂₃H₂₀BrF₃NO₅ requires 526.0471 and 528.0454).

Step 4: Preparation of [2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorophenoxy]acetic Acid

A solution of ethyl [2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorophenoxy]acetate (from Step 3) (0.62 g, 1.18 mmol), 1.5 N NaOH solution in 1:1 MeOH:water (1.2 mL, 1.77 mmol), and THF (1.2 mL) were refluxed at 60° C. for 1 h. The solution was concentrated on a rotary evaporator, cooled, and 5% citric acid added. The solid precipitate was filtered and dried in vacuo. Product obtained as a pale yellow solid (0.35 g, 60%). ¹H NMR (CD₃OD/400 MHz) δ 7.59 (m, 1H), 7.49 (m, 1H), 7.22 (m, 2H), 6.75 (m, 2H), 6.72 (s, 1H), 5.43 (s, 2H), 4.66 (s, 2H), 2.07 (s, 3H). ESHRMS m/z 498.0143 and 500.0186 (M+H calculated for C₂₁H₁₆BrF₃NO₅ requires 498.0158 and 500.0141).

Step 5: Preparation of 2-[2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorophenoxy]-N-ethylacetamide

To a cooled (−10° C.) solution of [2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorophenoxy]acetic acid (from Step 4) (0.15 g, 0.30 mmol) in DMA (2.0 mL) was added 4-methylmorpholine (0.04 mL, 0.36 mmol) and isobutyl chloroformate (0.05 mL, 0.36 mmol). Ethylamine (0.04 mL, 0.45 mmol) was added after 20 minutes. DMF removed by distillation after 1 h. Crude product purified by preparatory HPLC. Acetonitrile was evaporated and the solution washed with 5% NaHCO₃ (30 mL) and extracted in DCM (3×25 mL). The organic extracts were dried over Na₂SO₄, filtered, concentrated, and dried in vacuo to give a white solid (0.080 g, 51%). ¹H NMR (CD₃OD/400 MHz) 87.60 (m, 1H), 7.53 (t, 1H, J=8.0 Hz), 7.23 (t, 2H, J=8.4 Hz), 6.82 (m, 2H), 6.71 (s, 1H), 5.42 (s, 2H), 4.61 (s, 2H), 3.31 (q, 2H, J=6.4 Hz), 2.10 (s, 3H), 1.09 (t, 3H, J=7.2 Hz). ESHRMS m/z 525.0616 and 527.0568 (M+H calculated for C₂₃H₂₁BrF₃N₂O₄ requires 525.0631 and 527.0614).

Example 653

Methyl 3-[6-[(acetyloxy)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

Step 1: Preparation of 3-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-2-oxopropyl Acetate

A solution of 2,2,6-trimethyl-4H-1,3-dioxin-4-one (20 g, 141 mmol) in dry THF (400 mL) was cooled to −78° C. To this solution was slowly added a LiHMDS (1M-THF, 160 mL, 160 mmol). The resulting solution was maintained at −78° C. with stirring for 30 min. To the reaction mixture was added acetoxy acetylchloride (17 mL, 160 mmol) and the resulting mixture was maintained at −78° C. for at 1 h. The reaction was then allowed to slowly warm to rt and stir for an additional 1 h. The reaction was then quenched with addition of a 1N solution of ammonium chloride. The layers were sperated and the aqueous layer was extracted with ethyl acetate (5×). The organics were combined, dried, and concentrated in vacuo. The crude product was purified using a medium pressure liquid chromatography biotage system. Elution with hexanes-ethyl acetate (3:1) gave 13.1 g (38%) of a red-brown oil. The product looks clean by NMR. ¹H NMR (300 MHz, CDCl₃) δ 5.42 (s, 1H), 4.75 (s, 2H), 3.41 (s, 2H), 2.22 (s, 3H), 1.75 (s, 6H).

Step 2: Preparation of Methyl 3-[6-[(acetyloxy)methyl]-4-hydroxy-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

To a 100 mL RBF containing methyl 3-amino, 4-methylbenzoate (1.65 g, 10 mmol) was added the enone from Step 1(2.6 g, 10.7 mmol). The mixture was then dissolved in toluene (40 mL), fitted with a reflux condenser, and placed in an oil bath preset to 115° C. The mixture was heated to reflux for 1.5 h. The reaction flask was removed from the oil bath and a catalytic amount of TFA (5-6 drops) was added. The reaction was placed back in the oil bath and heated to reflux for an additional 2 h. The reaction was then allowed to cool to 0° C. The toluene was then removed under vacuum to give a thick brown residue. The residue was then dissolved in acetonitrile (10-15 mL) and allowed to stand. After 20-30 min a precipitate results which was filtered and washed with diethyl ether. After drying, an off-white solid (1.9 g, 57% yield) was obtained. ¹H NMR (300 MHz, DMSO_-d6) δ 7.94 (dd, J=7.8, 1.5 Hz, 1H), 7.73 (s, 1H), 7.54 (d, J=8.1 Hz, 1H), 6.19 (s, 1H), 5.73-5.71 (m, 1H), 4.47 (AB quar, J=10.5 Hz, 2H), 3.87 (s, 3H), 2.09 (s, 3H), 1.91 (s, 3H). ES-HRMS m/z 332.1096 (M+H calcd for C₁₇H₁₈NO₆ requires 332.1129).

Step 3: Preparation of Methyl 3-[6-[(acetyloxy)methyl]-3-bromo-4-hydroxy-2-oxopyridin-1(2H)-yl]4-methylbenzoate

To a slurry of the phenol (2.5 g, 7.5 mmol) in dry acetonitrile (50 mL), at rt, was added n-bromosuccinimide (1.33 g, 7.5 mmol). The resulting homogeneous mixture was stirred at rt for 3 h. The resulting precipitate was filtered and washed sequentially with acetonitrile and the diethyl ether. The product was dried in a vacuum oven to yield an off-white solid (2.5 g, 81%). ¹H NMR (300 MHz, DMSO_-d6) δ 11.82 (s, 1H), 7.97 (dd, J=7.8, 1.5 Hz, 1H), 7.80 (d, J=1.5 Hz, 1H), 7.57 (d, J=8.1 Hz, 1H), 6.38 (s, 1H), 4.49 (AB quar, J=13.8 Hz, 2H), 3.87 (s, 3H), 2.08 (s, 3H), 1.92 (s, 3H). ES-HRMS m/z 410.0225 (M+H calcd for C₁₇H₁₇NBrO₆ requires 410.0234).

Step 4: Preparation of the title compound. To a solution of the above phenol (2.5 g, 6.0 mmol) in dry DMF (25 mL) was added solid potassium carbonate (804 mg, 6.0 mmol). To this mixture was then added, via syringe, 2,4-diflourobenzyl bromide (783 μL, 6.0 mmol). The resulting mixture was allowed to stir at rt overnight. The reaction was then poured into ice water and stirred vigorously. The resulting precipitate was filtered and washed sequentially with water and diethyl ether. The solid was dried in a vacuum oven to yield an off-white solid (3.3 g, 99%). ¹H NMR (400 MHz, DMSO_-d6) δ 7.97 (dd, J=7.6, 1.2 Hz, 1H), 7.83 (d, J=1.6 Hz, 1H), 7.71 (q, J=8.8 Hz, 1H), 7.57 (d, J=8.0 Hz, 1H), 7.37 (dt, J=10.4, 2.4 Hz, 1H), 7.21 (dt, J=8.4, 2.0 Hz, 1H), 6.90 (s, 1H), 5.40 (s, 2H), 4.57 (AB quar, J=13.6 Hz, 2H), 3.86 (s, 3H), 2.07 (s, 3H), 1.90 (s, 3H). ES-HRMS m/z 536.0484 (M+H calcd for C₂₄H₂₁NF₂BrO₆ requires 536.0515).

Example 654

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-(2H)-yl]-4-methylbenzoic Acid

To a stirred suspension, at rt, of the Example 643 (2.0 g, 3.7 mmol) in THF (10 mL) was added a solution of 2.5N NaOH (3 mL, 7.5 mmol). The resulting homogeneous solution was stirred for 2 h. The reaction was judged complete and 1N HCl was added dropwise until a pH 4 was obtained. The reaction was then diluted with CH₂Cl₂ (10 mL). The resulting precipitate was filtered with additional washing from CH₂Cl₂. The solid was dried in a vacuum oven to yield a pure white solid (1.8 g, 99%). ¹H NMR (300 MHz, DMSO_-d6) δ 7.95 (dd, J=7.8, 1.8 Hz, 1H), 7.74-7.66 (m, 2H), 7.54 (d, J=8.1 Hz, 1H), 7.37 (dq, J=7.8, 2.7 Hz, 1H), 7.24-7.17 (m, 1H), 6.72 (s, 1H), 5.39 (s, 2H), 3.83 (AB quar, J=15.6 Hz, 2H), 2.02 (s, 3H). ES-HRMS m/z 480.0253 (M+H calcd for C₂₁H₁₇NF₂BrO₅ requires 480.0253).

Example 655

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide

To a slurry of Example 654 (500 mg, 1.04 mmol) in anhydrous CH₂Cl₂ was added Et₃N (218 μL, 1.56 mmol) and the resulting homogeneous mixture was stirred at rt. To this mixture was then added ethanolamine (70 μL, 1.14 mmol) via syringe. HOBt (155 mg, 1.14 mmol) was then added followed by addition of EDC (217 mg, 1.14 mmol). The reaction was allowed to stir overnight at rt. The reaction was quenched by addition of a solution of 1N NH₄Cl. The biphasic mixture was separated and the aqueous layer was extracted with CH₂Cl₂ (4×). The organics were combined, dried, and concentrated in vacuo. The resulting residue was purified by flash chromatography on a 16 g Michele-Miller column. Elution with CH₂Cl₂-MeOH (10:1□ 12:1) resulted in obtaining the desired product as a viscous oil. The oil was then dissolved in a CH₃CN-Et₂O combination. After 5-10 minutes, a precipitate resulted which upon filtration and drying yielded a pure white solid (210 mg, 40%). ¹H NMR (300 MHz, DMSO_-d6) δ 8.46 (t, J=5.2 Hz, 1H), 7.88 (dd, J=8.0, 2.0 Hz, 1H), 7.72-7.65 (m, 2H), 7.50 (d, J=8.4 Hz, 1H), 7.37 (dq, J=9.6, 2.4 Hz, 1H), 7.20 (dq, J=7.6, 1.6 Hz, 1H), 6.71 (s, 1H), 5.68 (t, J=5.6 Hz, —OH), 5.40 (s, 2H), 4.73 (t, J=5.6 Hz, —OH), 4.02 (dd, J=16.4, 5.6 Hz, 1H), 3.70 (dd, J=16.4, 5.6 Hz, 1H), 3.52-3.48 (m, 2H), 3.39-3.25 (m, 2H), 2.00 (s, 3H). ES-HRMS m/z 523.0674 (M+H calcd for C₂₃H₂₂N₂F₂BrO₅ requires 523.0675).

Example 656

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

The titled compound was prepared from the acid Example 654 (550 mg, 1.07 mmol) in a similar manner to the amide described above using EDC (245 mg, 1.28 mmol), HOBt (171 μL, 1.28 mmol), Et₃N (225 mL, 1.6 mmol), and 2.0M MeNH₂-THF (1.2 μL, 2.48 mmol). Following work-up with 1N NH₄Cl the product was precipitated out of the biphasic mixture after dilution with additional CH₂Cl₂ to give a white solid (250 mg, 51% yield). %). ¹H NMR (300 MHz, DMSO_-d6) δ 8.48 (quar, J=4.5 Hz, 1H), 7.88 (dd, J=8.1, 1.8 Hz, 1H), 7.72 (app quar, J=6.6 Hz, 1H), 7.63 (d, J=1.8 Hz, 1H), 7.52 (d, J=8.1 Hz, 1H), 7.37 (dt, J=10.2, 2.4 Hz, 1H), 7.20 (app dt, J=8.4, 1.8 Hz, 1H), 6.74 (s, 1H), 5.71 (t, J=5.4 Hz, 1H), 5.42 (s, 2H), 4.03 (dd, J=13.8, 5.1 Hz, 1H), 3.72 (dd, J=16.4, 5.1 Hz, 1H), 2.78 (d, J=4.5 Hz, 3H), 2.02 (s, 3H). ES-HRMS m/z 493.0575 (M+H calcd for C₂₂H₂₀N₂F₂BrO₄ requires 493.0569).

Example 657

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]-4-methylbenzamide

To a stirred suspension, at rt, of the carboxylic acid Example 654 (400 mg, 0.80 mmol) in anhydrous THF (4 mL) was added 4-methylmorpholine (274 μL, 2.5 mmol). To the resulting heterogeneous solution was then added 2-Chloro-4,6-dimethyltriazine (170 mg, 1.0 mmol) and the mixture was allowed to stir for 1 h at rt. Ammonium hydroxide solution (28-32%, 2 mL) was then added to the reaction and it was allowed to stir at rt overnight. The reaction was then worked up by diluting with H₂O (2-3 mL) and stirring vigorously. The resulting precipitate was filtered and washed with H2O and then diethyl ether. After drying with a vacuum oven an off-white solid (140 mg, 32%) was obtained. %). ¹H NMR (300 MHz, DMSO_-d6) δ 7.99-7.80 (m, 2H), 7.76 (m, 3H), 7.52 (d, J=8.1 Hz, 1H), 7.43-7.39 (m, 2H), 7.52 (d, J=8.1 Hz, 1H), 7.43-7.36 (m, 2H), 7.20 (dt, J=8.7, 1.8 Hz, 1H), 6.74 (s, 1H), 5.41 (s, 2H), 4.02-3.62 (m, 2H), 2.03 (s, 3H). ES-HRMS m/z 479.0411 (M+H calcd for C₂₁H₁₈N₂F₂BrO₄ requires 479.0413).

Example 658

(5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2-methyl-5-[(methylamino)carbonyl]phenyl}-6-oxo-1,6-dihydropyridin-2-yl)methyl Acetate

To a solution of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide (225 mg, 0.50 mmol) stirred in CH₂Cl₂ was added pyridine (55 μL, 0.69 mmol). To the resulting homogeneous solution was then added acetic anhydride (47 μL, 0.51 mmol). The mixture was stirred at rt for 3 h. Additional pyridine (150 μL, 1.8 mmol) and acetic anhydride (100 μL, 1.05 mmol) were then added and the reaction was allowed to stir overnight at rt. The reaction was then quenched with 1N NHCl₄ and diluted with CH₂Cl₂. The layers were separated and the organic layer was then extracted with CH₂Cl₂ (3×). The organics were then combined, dried, and concentrated in vacuo. The residue was then triturated with Et₂O and filtered to give (150 mg, 61%) an off-white solid. ¹H NMR (300 MHz, DMSO_-d6) δ 8.48 (br s, 1H), 7.87 (app d, J=7.8 Hz, 1H), 7.74-7.69 (m, 2H), 7.52 (d, J=7.5 Hz, 1H), 7.40 (app t, J=8.1 Hz, 1H), 7.28-7.19 (m, 1H), 6.91 (s, 1H), 5.43 (s, 2H), 4.60 (s, 2H), 2.79 (s, 3H), 2.06 (s, 3H), 1.94 (s, 3H). ES-HRMS m/z 535.0676 (M+H calcd for C₂₄H₂₂N₂F₂BrO₅ requires 535.0675).

Example 659

(2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methylbut-2-enamide

Step 1, (2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]but-2-enoic acid: The carboxylic acid compo was prepared by stirring the ester (900 mg, 2.1 mmol) in THF (10 mL). To this solution was added 1N NaOH (1 mL) and the resulting mixture was stirred at rt. After 2 h, additional NaOH (1 mL) was added to the reaction and then allowed to stir at rt overnight. The THF was then concentrated under vacuum. The remaining aqueous layer was then acidified to pH ˜4 after which a white precipitate resulted. Filtration and drying under vacuum gave rise to a white solid (900 mg) that was used as in the next step.

The titled compound was prepared by stirring the above acid (480 mg, 1.16 mmol) in CH₂Cl₂ at rt. To this mixture was added sequentially Et₃N (244 μL), HOBt (188 mg, 1.4 mmol), MeNH₂ (2.0M-THF, 700 mL, 1.4 mmol), and finally EDC (266 mg, 1.4 mmol). The homogeneous mixture was then allowed to stir at rt overnight. The reaction was quenched with 1N HCl. The layers were separated and the aqueous layer was extracted with CH₂Cl₂ (4×). The organics were combined, dried, and concentrated in vacuo. The crude residue was triturated in CH₃CN-Et₂O combination and filtered to give a pure white solid (330 mg, 67%). ¹H-NMR (DMSO_d6/300 MHz) δ 8.20-7.90 (m, 1H), 7.68 (q, J=8.4 hz, 1H); 7.37 (dt, J=10.2, 2.4 Hz, 1H); 7.20 (dt, J=15.6, 4.2 Hz, 1H); 6.60 (s, 1H), 5.63 (d, J=15.6 Hz, 1H), 5.31 (s, 2H), 4.81 (d, J=2.7 Hz, 2H), 3.33 (d, J=6.9 Hz, 1H), 2.61 (d, J=4.8 Hz, 3H), 2.37 (s, 3H). ES-HRMS m/z 427.0493 (M+H calcd for C₁₈H₁₈BrF₂N₂O₃=427.0463).

Example 660

Methyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furoate

Step 1: To a room temperature suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (330.1 mg, 1.00 mmol)) and NaH (48.0 mg, 2.0 mmol) in THF (1.6 mL) was added methyl-5-chloromethyl-2-furate (400 mg, 2.30 mmol). The resulting suspension was stirred and heated to 68° C. for 8 hours until complete consumption of starting material by LCMS analysis. The reaction mixture was then diluted with ammonium chloride (saturated aqueous solution, 10 mL) and water (100 mL). This resulting emulsion was then extracted with with ethyl acetate (3×300 mL). The resulting organic extract was separated, Na₂SO₄ dried, and concentrated. The resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (3:7) to furnish a solid. ¹H NMR (400 MHz, CDCl₃) δ 7.53 (app q, J=8.2 Hz, 1H), 7.07 (d, J=3.5 Hz, 1H), 6.93 (app dt, J=8.4, 1.5 Hz, 1H), 6.84 (app ddd, J=10.2, 8.7, 2.4 Hz, 1H), 6.53 (d, J=3.4 Hz, 1H), 6.00 (s, 1H), 5.27 (s, 2H), 5.18 (s, 2H), 3.85 (s, 3H), 2.54 (s, 3H); LC/MS C-18 column, t_r=2.64 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 468 (M+H). ES-HRMS m/z 468.0276 (M+H calcd for C₂₀H₁₇BrF₂NO₅ requires 468.0253).

Example 661

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-(hydroxymethyl)-N-methylbenzamide

Step 1: Preparation of 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzoic Acid

To a room temperature solution of methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzoate (1.05 g, 2.02 mmol) in THF (10.0 mL) was added dropwise an aqueous solution of sodium hydroxide (3.0 M, 3.5 mL, 10 mmol). The reaction was then heated to 60° C. for 8.0 hours. The resulting suspension was then diluted with 500 mL of ethyl acetate and neutralized with an aqueous solution of hydrochloric acid (2.0 N, 5.0 mL, 10 mmol). The resulting biphasic solution was separated and the resulting aqueous layer was further extracted with ethyl acetate (2×200 mL). The resulting combined organic extracts were Na₂SO₄ dried, filtered and concentrated in vacuo to a volume of 50 mL. At this time a white solid began to form and the resulting solid suspension was allowed to sit until precipitation appeared to stop (approximately 1.0 hour). The precipitate was collected and dried in vacuo (1.0 mm Hg) to furnish the solid acid as an intermediate (806 mg, 78%). ¹H NMR (400 MHz, d₇-DMF) δ 13.19 (s, 1H), 8.63 (app d, J=4.5 Hz, 1H), 8.09 (d, J=8.0 Hz, 1H), 8.00 (dd, J=8.0, 1.6 Hz, 1H), 7.71-7.67 (m, 2H), 7.34 (app dt, J=9.6, 1.6 Hz, 1H), 7.16 (app dt, J=8.7, 1.8 Hz, 1H), 6.66 (s, 1H), 5.33 (s, 2H), 3.29 (s, 3H), 1.92 (s, 3H); LC/MS C-18 column, t_r=2.15 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 507 (M+H). ES-HRMS m/z 507.0344 (M+H calcd for C₂₂H₁₈BrF₂N₂O₅ requires 507.0362).

Step 2: Preparation of the title compound. To a 0° C. solution of 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzoic acid (500 mg, 0.986 mmol) in THF (6.8 mL) was added dropwise a solution of borane-dimethyl sulfide complex (THF solution, 2.0 M, 2.0 mL, 4.0 mmol). The internal temperature of the reaction was never allowed to exceed 0° C. The resulting solution was maintained for 4.0 hours, at which time the cooling bath was removed and the reaction was maintained at room temperature for an additional two hours. Next, a solution of ammonium chloride (saturated aqueous, 300 mL) was added. The resulting emulsion was extracted with ethyl acetate (3×300 mL) and the resulting organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo to a residue that was subjected to SiO₂ chromatography with ethyl acetate/hexanes (6:4) to furnish a solid (392 mg, 81%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.96 (dd, J=8.0, 1.9 Hz, 1H), 7.75 (d, J=8.1 Hz, 1H), 7.65 (app q, J=8.0 Hz, 1H), 7.58 (d, J=1.7 Hz, 1H), 7.05 (app t, J=8.5 Hz, 2H), 6.64 (s, 1H), 5.36 (s, 2H), 4.35 (AB-q, J=14.1 Hz, Δ=60.8 Hz, 2H), 2.90 (s, 3H), 2.03 (s, 3H); LC/MS C-18 column, t_r=2.16 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 493 (M+H). ES-HRMS m/z 493.0590 (M+H calcd for C₂₂H₂₀BrF₂N₂O₄ requires 493.0596).

Example 662

2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N′-dimethylterephthalamide

Step 1: To a room temperature solution of 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzoic acid (500 mg, 0.986 mmol) in DMF (5.0 mL) was added 1-(3-dimethylaminopropyl)-ethylcarbodiimide hydrochloride (EDC-HCl, 350.0 mg, 1.83 mmol) and 1-hydroxy-benzotriazole (HOBT, 100.0 mg, 0.74 mmol) sequentially. To this resulting suspension was then added a solution of methylamine (2.0 M THF, 1.0 mL, 2.0 mmol). The reaction was stirred for 16.0 hours, at which time the reaction was diluted with ethyl acetate (600 mL). The mixture was washed with (3×200 mL) of water and the organic extract was separated, Na₂SO₄ dried, and concentrated in vacuo to a volume of approximately 60 mL. At this time a solid precipitate formed and was collected to furnish (289 mg, 56%). ¹H NMR (300 MHz, d₄-MeOH) δ 8.06 (br d, J=8.0 Hz, 1H), 7.81 (d, J=8.1 Hz, 1H), 7.73 (s, 1H), 7.70 (app q, J=7.4 Hz, 1H), 7.09 (app t, J=8.0 Hz, 2H), 6.65 (s, 1H), 5.39 (s, 2H), 2.96 (s, 3H), 2.79 (s, 3H), 2.13 (s, 3H); LC/MS C-18 column, t_r=2.13 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 520 (M+H). ES-HRMS m/z 520.0700 (M+H calcd for C₂₃H₂₁BrF₂N₃O₄ requires 520.0678).

Example 663

2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-4-methylterephthalamide

Step 1: To a room temperature suspension of 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzoic acid (302 mg, 0.595 mmol) in THF (1.8 mL) was added 2-chloro-4,6 dimethoxy-1,3,5 triazine (140.5 mg, 0.800 mmol) and N-methyl morpholine (NMM, 184 mg, 1.824 mmol) sequentially. The resulting solution was matured for 2 hours and then a saturated aqueous solution of ammonium hydroxide (0.60 mL) was added. The reaction was allowed to continue for 1 additional hour at which time a precipitate formed which was collected, washed with 20 mL of diethyl ether, and dried in vacuo to furnish a solid (201 mg, 66%). ¹H NMR (400 MHz, d₆-DMSO) δ 8.59 (br d, J=8.0, 1H), 7.96 (d, J=8.0 Hz, 1H), 7.83 (s, 1H), 7.72 (d, J=9.0, 1H), 7.69-7.64 (m, 2H), 7.39-7.31 (m, 1H), 7.19 (app t, J=8.0 Hz, 1H), 6.60 (s, 1H), 5.31 (s, 2H), 3.85 (s, 1H), 2.78 (br d, J=8.0 Hz, 3H), 1.96 (s, 3H); LC/MS C-18 column, t_r=2.20 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 506 (M+H). ES-HRMS m/z 506.0550 (M+H calcd for C₂₂H₁₉BrF₂N₃O₄ requires 506.0522).

Example 664

Methyl 4-(aminocarbonyl)-2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate

Step 1: To a room temperature solution of 3-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-4-(methoxycarbonyl)benzoic acid (3.01 g, 9.93 mmol) in DMF (20 mL) was added 1-(3-dimethylaminopropyl)-ethylcarbodiimide hydrochloride (EDC-HCl, 2.00 g, 10.4 mmol) and 1-hydroxy-benzotriazole (HOBT, 50.0 mg, 0.367 mmol) sequentially. To this resulting suspension was then added a solution of ammonia (0.5 M 1,4 dioxane, 30.0 mL, 15.0 mmol). The reaction was stirred for 16.0 hours until complete consumption of starting material was seen by LCMS analysis. At this time the reaction vessel was placed on a roto-evaporator at 30 mm Hg vacuum and maintained at 30° C. for 30 minutes to strip off any residual ammonia from the reaction mixture. The reaction vessel was removed from the roto-evaporator and subsequently charged with solid N-bromosuccinimide (1.790 g, 10.06 mmol) and the resulting reddish solution was stirred for 3.0 hours. At this time the reaction was charged with K₂CO₃ (3.00 g, 21.7 mmol) and 2,4 difluorobenzyl bromide (1.95 mL, 15.2 mmol). The resulting suspension was stirred for 16.0 hours. At this time the reaction suspension was diluted with water (400 mL) and extracted with ethyl acetate (3×300 mL). The organic extracts were separated, Na₂SO₄ dried, and concentrated to a residue that was subjected to SiO₂ chromatography using ethyl acetate/hexanes/methanol (6:3.5:0.5) to furnish an off white solid (1.09 g, 21%). ¹H NMR (400 MHz, d₄-MeOH) δ 8.21 (dd, J=8.5, 1.5 Hz, 1H), 8.09 (dd, J=7.6, 2.0 Hz, 1H), 7.78 (br s, 1H), 7.65 (app q, J=7.9 Hz, 1H), 7.03 (app t, J=8.0 Hz, 2H), 6.63 (s, 1H), 5.37 (s, 2H), 3.75 (s, 3H), 2.02 (s, 3H); LC/MS C-18 column, t_r=2.28 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 507 (M+H). ES-HRMS m/z 507.0385 (M+H calcd for C₂₂H₁₈BrF₂N₂O₅ requires 507.0362).

Example 665

2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N¹,N¹,N⁴-trimethylterephthalamide

Step 1: To a room temperature solution of 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzoic acid (300 mg, 0.591 mmol) in DMF (1.8 mL) was added 1-(3-dimethylaminopropyl)-ethylcarbodiimide hydrochloride (EDC-HCl, 190.0 mg, 1.0 mmol) and 1-hydroxy-benzotriazole (HOBT, 26.0 mg, 0.191 mmol) sequentially. To this resulting suspension was then added a solution of dimethylamine (2.0 M THF, 0.50 mL, 1.0 mmol). The reaction was stirred for 16.0 hours, at which time the reaction mixture was directly applied to SiO₂ chromatography with ethyl acetate/hexanes (6:4) to furnish a solid (206 mg, 65%). ¹H NMR (400 MHz, d₄-MeOH) δ 8.01 (dd, J=8.2, 1.5 Hz, 1H), 7.73 (app d, J=8.1 Hz, 1H), 7.61 (app q, J=7.2 Hz, 1H), 7.60 (app d, J=9.5 Hz, 1H), 7.04 (app t, J=8.0 Hz, 2H), 6.65 (s, 1H), 5.32 (s, 2H), 3.64 (s, 3H), 2.92 (s, 6H), 2.13 (s, 3H); LC/MS C-18 column, t_r=2.20 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 m/min with detection 254 nm, at 50° C.). ES-MS m/z 534 (M+H). ES-HRMS m/z 534.0820 (M+H calcd for C₂₄H₂₃BrF₂N₃O₄ requires 534.0835).

Example 666

2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)carbonyl]benzyl Carbamate

Step 1: To a room temperature solution of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-(hydroxymethyl)-N-methylbenzamide (493 mg, 1.00 mmol) in methylene chloride (5.0 mL) was added a solution of trichloroacetyl isocyanate (toluene, 0.53 M, 1.9 mL, 1.0 mmol). The resulting solution was stirred for one hour until complete consumption of starting material by LCMS analysis. The reaction mixture was then directly applied to Al₂O₃ (0.5 g of activity type I) and the slurry was matured for three hours. At this time, the Al₂O₃ plug was flushed with ethyl acetate/methanol (95:5) and the resulting mother liquor was concentrated to a residue that was subjected to SiO₂ chromatography using ethyl acetate/hexanes/methanol (6:3.5:0.5) to furnish a white solid (396 mg, 74%). ¹H NMR (300 MHz, d₄-MeOH) δ 8.00 (dd, J=8.0, 1.7 Hz, 1H), 7.75 (d, J=8.2 Hz, 1H), 7.72-7.64 (m, 2H), 7.09 (app t, J=8.5 Hz, 2H), 6.69 (s, 1H), 5.40 (s, 2H), 4.85 (m, 2H), 2.90 (s, 3H), 2.10 (s, 3H); LC/MS C-18 column, t_r=2.15 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 536 (M+H). ES-HRMS m/z 536.0617 (M+H calcd for C₂₃H₂₁BrF₂N₃O₅ requires 536.0627).

Example 667

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-vinylphenyl)-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-vinylphenyl)-6-methylpyridin-2(1H)-one

To a room temperature solution of 1-(4-bromo-2,6-difluorophenyl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (4.01 g, 9.06 mmol) in anhydrous THF (30 mL) was added, sequentially, tributyl(vinyl)tin (5.00 g, 15.7 mmol) and tetrakis(tripheylphosphine)palladium (1.00 g, 0.865 mmol) under an argon stream. The reaction vessel was then equipped with a reflux condenser and the reaction system purged with an argon flow. The resulting yellow solution was heated to 68° C. and stirred under a positive pressure of argon for 12.0 hours until complete disappearance of starting material by LCMS analysis. The reaction mixture was diluted with 300 mL of brine and extracted with ethyl acetate (3×300 mL). The organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo and the resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (1:1) to furnish a yellowish solid (3.18 g, 90%). ¹H NMR (400 MHz, CDCl₃) δ 7.41 (app q, J=8.0 Hz, 1H), 7.08 (app d, J=8.3 Hz, 2H), 6.90 (app t, J=7.2 Hz, 1H), 6.85 (app t, J=7.4 Hz, 1H), 6.63 (dd, J=17.5, 10.9 Hz, 1H), 5.96 (app d, 15.8 Hz, 1H), 5.94 (app d, J=15.8 Hz, 1H), 5.79 (d, J=17.4 Hz, 1H), 5.43 (d, J=10.9 Hz, 1H), 5.01 (br s, 2H), 1.99 (s, 3H); LC/MS C-18 column, t_r=2.93 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 390 (M+H). ES-HRMS m/z 390.1095 (M+H calcd for C₂₁H₁₆F₄NO₂ requires 390.1112).

Step 2: To a briskly stirred room temperature solution of 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-vinylphenyl)-6-methylpyridin-2(1H)-one (721 mg, 1.85 mmol) in methylene chloride (10 mL) was added solid N-bromosuccinimide (330 mg, 1.86 mmol) and the resulting reddish solution was stirred for 10 minutes. At this time the reaction was diluted with ethyl acetate (100 mL) and washed with sodium sulfite (5% aqueous solution, 50 mL) The resulting organic extracts were Na₂SO₄ dried, filtered, and concentrated in vacuo to approximately 50 mL volume. The resulting mother liquor rapidly precipitated and furnished an amorphous solid that was collected and dried at 1 mm Hg vacuum to provide the desired product as a solid (610 mg, 70%). ¹H NMR (400 MHz, CDCl₃) δ 7.59 (app q, J=8.0 Hz, 1H), 7.09 (app d, J=8.3 Hz, 2H), 6.95 (app t, J=7.2 Hz, 1H), 6.87 (app t, J=7.4 Hz, 1H), 6.62 (dd, J=17.5, 10.9 Hz, 1H), 6.12 (s, 1H), 5.81 (d, J=17.4 Hz, 1H), 5.43 (d, J=10.9 Hz, 1H), 5.25 (br s, 2H), 2.07 (s, 3H); LC/MS C-18 column, t_r=3.17 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 468 (M+H). ES-HRMS m/z 468.0249 (M+H calcd for C₂₁H₁₅BrF₄NO₂ requires 468.0217).

Example 668

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2,6-difluorophenyl]-6-methylpyridin-2(1H)-one

Step 1: Preparation of the title compound. To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-vinylphenyl)-6-methylpyridin-2(1H)-one (408.0 mg, 0.871 mmol) in water/acetone 1:3 (8.0 mL) was added, sequentially, N-methyl morpholine oxide (268.0 mg, 2.29 mmol) and osmium tetroxide (4% water solution, 0.25 mL or approximately 10 mg, 0.039 mmol). The resulting solution was stirred for 8 hours until complete consumption of starting material by LCMS analysis, and the reaction was concentrated in vacuo to one-fourth original volume. The resulting solution was diluted with ethyl acetate (300 mL) and washed with water (2×100 mL). The organic extract was separated, Na₂SO₄ dried, and concentrated in vacuo and the resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes/methanol (6:3.5:0.5) to furnish a solid (389 mg, 88%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.62 (app q, J=8.0 Hz, 1H), 7.26 (dd, J=9.6, 4.5 Hz, 2H), 7.04 (app t, J=8.6 Hz, 2H), 6.67 (s, 1H), 5.36 (s, 2H), 4.75 (app t, J=5.6 Hz, 1H), 3.68-3.61 (m, 2H), 2.11 (s, 3H); LC/MS C-18 column, t_r=2.26 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 m/min with detection 254 nm, at 50° C.). ES-MS m/z 502 (M+H). ES-HRMS m/z 502.0247 (M+H calcd for C₂₁H₁₇BrF₄NO₄ requires 502.0272).

Example 669

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzaldehyde

Step 1: Preparation of the title compound. To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2,6-difluorophenyl]-6-methylpyridin-2(1H)-one (310 mg, 0.615 mmol) in toluene (3.0 mL) was added lead(IV) acetate (443 mg, 1.63 mmol). The resulting dark brown solution was stirred for one hour until complete consumption of starting material by LCMS analysis. The reaction mixture was then diluted with ethyl acetate (100 mL), water washed (3×100 mL), and brine washed (3×30 mL). The resulting organic extract was separated, Na₂SO₄ dried, and concentrated. The resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (1:1) to furnish a light yellow solid (269 mg, 93%). Caution, product is easily air oxidized. ¹H NMR (300 MHz, d₄-MeOH) δ 10.05 (s, 1H), 7.68 (app q, J=7.2 Hz, 1H), 7.38 (d, J=8.0 Hz, 2H), 7.05 (app t, J=8.2 Hz, 2H), 6.73 (s, 1H), 5.40 (s, 2H), 2.15 (s, 3H); LC/MS C-18 column, t_r=2.72 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 470 (M+H). ES-HRMS m/z 470.0049 (M+H calcd for C₂₀H₁₃BrF₄NO₃ requires 470.0009).

Example 670

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzyl Carbamate

Step 1: To a room temperature solution of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzaldehyde (220 mg, 0.468 mmol) in methanol (10 mL) was added solid sodium borohydride (60.0 mg, 1.58 mmol). The resulting solution evolved gas for approximately 0.5 minute and was stirred for 10 additional minutes until complete consumption of starting material by LCMS analysis. The reaction was then diluted with saturated aqueous solution of ammonium chloride (10 mL) and extracted with ethyl acetate (4×50 mL). The organic extract was separated, Na₂SO₄ dried, and concentrated to a residue. This resulting residue was then diluted with methylene chloride (5.0 mL) and a solution of trichloroacetyl isocyanate (toluene, 0.53 M, 1.0 mL, 0.53 mmol) was added. The resulting solution was stirred for one hour until complete consumption of starting material by LCMS analysis. The reaction mixture was then directly applied to Al₂O₃ (0.5 g of activity type I) and the slurry was matured for three hours. At this time, the Al₂O₃ plug was flushed with ethyl acetate/methanol (95:5) and the resulting mother liquor was concentrated to a residue that was subjected to SiO₂ chromatography using ethyl acetate/hexanes/methanol (6:3.8:0.2) to furnish a white solid (181 mg, 75%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.63 (app q, J=8.0 Hz, 1H), 7.43 (d, J=8.2 Hz, 2H), 7.04 (app t, J=8.1 Hz, 2H), 6.68 (s, 1H), 5.37 (s, 2H), 5.12 (m, 2H), 2.11 (s, 3H); LC/MS C-18 column, t_r=2.54 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 515 (M+H). ES-HRMS m/z 515.0232 (M+H calcd for C₂₁H₁₆BrF₄N₂O₄ requires 515.0234).

Example 671-687

The following compounds are prepared essentially according to the procedures outlined in the schemes and the above examples.

Example No.
671
672
673
674
675
676
677
678
679
680
681
682
683
684
685
686
687
688
689
690
691
692
693
694
695
696
697
698
699
700

Example 701

N-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-2-hydroxyacetamide

Step 1. Preparation of 1-[4-(aminomethyl)benzyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

The compound of Example 606 (10.0 g, 23.38 mmol) was suspended in tetrahydrofuran (100 mL) and cooled in an ice-bath. Borane dimethyl sulfide (29.9 mL, 2.0 M in tetrahydrofuran, 59.7 mmol) was added. The resulting mixture was heated to reflux overnight and then cooled in an ice-bath. Additional borane dimethyl sulfide (5.85 mL, 2.0 M in tetrahydrofuran, 11.7 mmol) was added. The resulting mixtue was heated to reflux overnight and the cooled to room temperature. The flask was fitted with a distillation head and the reaction was partially concentrated. Additional borane dimethyl sulfide (5.85 mL, 2.0 M in tetrahydrofuran, 11.7 mmol) was added. The mixture was heated to reflux overnight and the cooled in an ice-bath. The reaction was quenched by the addition of 1.0 N HCl (75.0 mL) then partially concentrated. The aqueous layer was made alkaline with 2.5 N NaOH and a precipitate developed. The solid was collected by filtration washing with diethyl ether to give a pale purple solid (3.00 g, 32%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.64 (app q, J=7.9 Hz, 1H), 7.44 (d, J=7.9 Hz, 2H), 7.32 (app dt, J=2.4, 9.9 Hz, 1H), 7.14 (app dt, J=1.9, 8.5 Hz, 1H), 7.13 (d, J=7.9 Hz, 2H), 6.61 (s, 1H), 5.27 (s, 4H), 3.90 (s, 2H), 2.29 (s, 3H).

Step 2. Preparation of N-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-2-hydroxyacetamide

Acetoxyacetic acid (1.46 g, 12.35 mmol) was dissolved in N,N-dimethylformamide (30 mL) and 1-Hydroxybenzotriazole (1.84 g, 13.59 mmol) was added followed by 4-methylmorpholine (2.04 mL, 18.53 mmol), 1-[4-(aminomethyl)benzyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (1-[4-(aminomethyl)benzyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one compound of step 1) (2.50 g, 6.18 mmol) and then 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (2.84 g, 14.83 mmol). The resulting mixture was stirred at room temperature for 1 hour at which time the reaction was diluted with H₂O (100 mL). The reaction mixture was then extracted with ethyl acetate. The combined organic extracts were washed with saturated NaHCO₃, brine, dried over Na₂SO₄, filtered and concentrated. Chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) provided a white foam. The resulting foam was dissolved in 10% aqueous methanol (20 mL). K₂CO₃ (0.653 g, 4.73 mmol) was added and the mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated and H2O (50 mL) was added. The resulting precipitate was collected by filtration washing with diethyl ether to give an off-white solid (1.34 g, 47%). ¹H NMR (400 MHz, CDCl₃) δ 7.50 (app q, J=7.7 Hz, 1H), 7.27 (app t, J=5.8 Hz, 1H), 7.12 (d, J=8.1 Hz, 2H), 6.97 (d, J=8.1 Hz, 2H), 6.94-6.89 (m, 1H), 6.86-6.81 (m, 1H), 6.09 (s, 2H), 5.23 (s, 2H), 5.18 (s, 2H), 4.53 (t, J=5.8 Hz, 1H), 4.33 (d, J=5.9 Hz, 2H), 3.85 (d, J=5.6 Hz, 2H), 2.30 (s, 3H). ES-HRMS m/z 463.1256 (M+H calcd for C₂₃H₂₂ClF₂N₂O₄ requires 463.1231).

Example 702

N-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-1-hydroxycyclopropanecarboxamide

Preparation of N-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-1-hydroxycyclopropanecarboxamide. 1-Hydroxy-1-cyclopropane-carboxylic acid (1.26 g, 12.35 mmol) was dissolved in N,N-dimethylformamide (30 mL). 1-Hydroxybenzotriazole (1.84 g, 13.59 mmol) was added followed by 4-methylmorpholine (2.04 mL, 18.53 mmol), 1-[4-(aminomethyl)benzyl]-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (Example 701, step 1) (2.50 g, 6.18 mmol) and then 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (2.84 g, 14.83 mmol). The resulting mixture was stirred at room temperature for 24 hours at which time the reaction was diluted with H₂O (100 mL). The reaction mixture was then extracted with ethyl acetate. The combined organic extracts were washed with saturated NaHCO₃, brine, dried over Na₂SO₄, filtered and concentrated. Chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) provided a white foam. The resulting foam was dissolved in 10% aqueous methanol (20 mL) to provide an white foam (1.45 g, 48%). ¹H NMR (400 MHz, CDCl₃) δ 7.52-7.46 (m, 1H), 7.34 (t, J=5.9 Hz, 1H), 7.08 (d, J=8.2 Hz, 2H), 6.92 (app d, J=8.2 Hz, 2H), 6.92-6.89 (m, 1H), 6.86-6.81 (m, 1H), 6.11 (s, 1H), 5.22 (s, 2H), 5.18 (s, 2H), 4.30 (d, J=5.9 Hz, 2H), 2.28 (s, 3H), 1.11 (app q, J=4.1 Hz, 2H), 0.90 (app q, J=4.1 Hz, 2H). ES-HRMS m/z 489.1420 (M+H calcd for C₂₅H₂₄ClF₂N₂O₄ requires 489.1387).

Example 703

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl Carbamate

Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl Carbamate

Compound of Example 206 (0.868 g, 1.93 mmol) was suspended in dichloromethane (7.0 mL). Trichloroacetyl isocyanate (4.00 mL, 0.53 M in toluene, 2.12 mmol) was added. The resulting mixture was stirred at room temperature for 3 hours then diluted with tetrahydrofuran (50 mL) and A1203 (5.0 g) was added and the mixture was stirred at room temperature overnight. The reaction mixture was filtered through a pad of Celite® washing with methonal. The filtrate was then concentrated and the residue was redissolved in tetrahydrofuran (30 mL). Al₂O₃ (5.0 g) was added and the mixture was heated to 40° C. for 3 hours. After cooling to room temperature, the reaction was filtered through a pad of Celite® washing with methanol. The filtrate was concentrated and the resulting solid was washed with diethyl ether to give an off-white solid (0.831 g, 87%). ¹H NMR (400 MHz, CDCl₃) δ 7.54 (app q, J=7.7 Hz, 1H), 7.25 (d, J=8.2 Hz, 2H), 7.13 (d, J=8.2 Hz, 2H), 6.25 (app dt, J=2.0, 8.3 Hz, 1H), 6.86-6.30 (m, 1H), 5.97 (s, 1H), 5.32 (s, 2H), 5.18 (s, 2H), 5.02 (s, 2H), 4.81 (br s, 2H), 2.25 (s, 3H). ES-HRMS m/z 493.0580 (M+H calcd for C₂₂H₂₀BrF₂N₂O₄ requires 493.0569).

Example 704

2-[(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)amino]-1-methyl-2-oxoethyl Acetate

To a reaction vessel (borosilicate culture tube) was added compound of Example 611 (0.300 g, 0.69 mmol) and dichloromethane (3.0 mL). A stock solution of N-methylmorpholine (0.30 M, 3.0 mL) was added and the parallel reaction apparatus was then orbitally shaken (Labline Benchtop Orbital Shaker) at approximately 200 RPM at room temperature for 10 minutes. (S)-(−)-2-Acetoxypropionyl chloride (0.131 mL, 1.04 mmol) was then added to the reaction vessel and the reaction apparatus was orbitally shaken at room temperature for 1.5 hours. At this time the reaction was diluted with dichloromethane (20 mL) and treated with approximately 2.1 g of polyamine resin (2.63 mmol/g) and approximately 3.8 g of methylisocyanate fucntionalized polystyrene (1.10 mmol/g) and the orbital shaking was continued at 200 RPM at room temperature overnight. The reaction vessel was then opened and the solution Phase products were separated from the insoluble quenched byproducts by filtration and collection into a vial. After partial evaporation the insoluble byproducts were rinsed with dichloromethane (2×10 mL). The filtrate was evaporated by blowing N₂ over the vial to afford an off-white solid (0.375 g, 99%). ¹H NMR (400 MHz, DMF-d₆) δ 10.14 (s, 1H), 7.75 (app dt, J=6.98, 8.59 Hz, 1H), 7.67-7.64 (m, 2H), 7.30 (ddd, J=2.55, 9.26, 11.81 Hz, 1H), 7.21-7.17 (m, 3H), 6.61 (s, 1H), 5.37 (s, 4H), 5.11 (q, J=6.85 Hz, 1H), 2.40 (s, 3H), 2.10 (s, 3H), 1.46 (d, J=6.85 Hz, 3H). ES-HRMS m/z 549.0790 (M+H calcd for C₂₅H₂₃BrF₂N₂O₅ requires 549.0831).

Example 705

2-[(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)amino]-1,1-dimethyl-2-oxoethyl Acetate

By the method for Example 704 and substituting (S)-(−)-2-acetoxypropionyl chloride with 2-acetoxy-2-methylpropionyl chloride, the title, compound was prepared (0.380 g, 98%). ¹H NMR (400 MHz, DMF-d₆) δ 9.68 (s, 1H), 7.75 (app dt, J=6.72, 8.60 Hz, 1H), 7.71-7.68 (m, 2H), 7.30 (ddd, J=2.55, 9.40, 11.95 Hz, 1H), 7.21-7.15 (m, 3H), 6.61 (s, 1H), 5.37 (s, 4H), 2.41 (s, 3H), 2.04 (s, 3H), 1.59 (s, 6H). ES-HRMS m/z 563.1027 (M+H calcd for C₂₆H₂₅BrF₂N₂O₅ requires 563.0988).

Example 706

{1-[3-(aminocarbonyl)phenyl]-5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl Acetate

Step 1: Preparation of {1-[3-(aminocarbonyl)phenyl]-4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl}methyl Acetate

3-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-2-oxopropyl acetate (4.00 g, 16.52 mmol) was dissolved in 1,4-dioxane (160 mL) and 3-aminobenzamide (1.73 g, 12.71 mmol) was added. The reaction was heated to reflux for 1 hour then cooled to 70° C. Methanesulfonic acid (1.22 g, 12.71 mmol) was added and the reaction brought back to reflux for 1 hour. The reaction was cooled to room temperature, concentrated and used as crude product for the next step.

Step 2: Preparation of {1-[3-(aminocarbonyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl Acetate

{1-[3-(aminocarbonyl)phenyl]-4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate (crude from step 1) (3.61 g, 11.94 mmol) was dissolved in N,N-dimethylformamide (40 mL). K₂CO₃ (3.80 g, 27.46 mmol) was added followed by 2,4-difluorobenzyl bromide (5.44 g, 26.27 mmol). The reaction mixture was stirred for 48 hours at room temperature. The reaction mixture was then partially concentrated and the residue taken up in dichloromethane/tetrahydrofuran 1:1 and filtered. The filtrate was collected, concentrated and the residue tritrated with dichloromethane to afford a tan solid (1.64 g, 32%). ¹H NMR (400 MHz, DMF-d₆) δ 8.19 (br s, 1H), 8.07 (app dt, J=1.35, 7.66 Hz, 1H), 7.91 (app t, J=1.81 Hz, 1H), 7.76 (app dt, J=6.58, 8.59 Hz, 1H) 7.62 (t, J=7.79 Hz, 1H), 7.55 (ddd, J=1.21, 2.01, 7.79 Hz, 1H), 7.46 (br s, 1H), 7.34 (ddd, J=2.55, 9.40, 10.47 Hz, 1H), 7.23-7.18 (m, 1H), 6.26 (d, J=2.55 Hz, 1H), 6.11 (d, J=2.69 Hz, 1H), 5.23 (s, 2H), 4.62 (AB q, J_AB=14.97 Hz, 2H), 1.96 (s, 3H). ES-HRMS nm/z 429.1280 (M+H calcd for C₂₂H₁₈F₂N₂O₅ requires 429.1257).

Step 3: Preparation of the Title Compound

{1-[3-(aminocarbonyl)phenyl]-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate (from step 2) (1.02 g, 2.39 mmol) was suspended in dichloromethane (15 mL) and N-chlorosuccinimide (0.37 g, 2.75 mmol) was added. Dichloroacetic acid (0.10 ml, 1.22 mmol) was added and the reaction mixture was stirred at 40° C. for 1.5 hours. The reaction was cooled to room temperature and a precipitate formed. The reaction mixture was diluted with diethyl ether and the precipitate was collected by filtration and washed with diethyl ether (3×15 mL) to afford a tan solid (0.940 g, 85%). ¹H NMR (400 MHz, DMF-d₆) δ 8.21 (br s, 1H), 8.11 (app dt, J=1.48, 7.52 Hz, 1H), 7.95 (app t, J=1.61 Hz, 1H), 7.80 (app dt, J=6.72, 8.59 Hz, 1H) 7.69-7.60 (m, 2H), 7.48 (br s, 1H), 7.35 (ddd, J=2.55, 9.53, 10.61 Hz, 1H), 7.24-7.19 (m, 1H), 6.97 (s, 1H), 5.49 (s, 2H), 4.71 (AB q, J_AB=15.04 Hz, 2H), 1.98 (s, 3H). ES-HRMS m/z 463.0883 (M+H calcd for C₂₂H₁₇ClF₂N₂O₅ requires 463.0867).

Example 707

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-5-yl]methyl}pyridin-2(1H)-one

Step 1. Preparation of Methyl 2-(methylthio)pyrimidine-5-carboxylate

A solution of the sodium salt of 3,3-dimethoxy-2-methoxycarbonylpropen-1-ol (5.0 g, 25 mmol), 2-methyl-2-thiopseudourea sulfate (3.5 g, 25 mmol) in anhydrous methanol (25 mL) was refluxed for 3 hours under anhydrous conditions. The reaction mixture was cooled and diluted with ethyl acetate. The reaction mixture was filtered and the residue was washed with ethyl acetate. The filtrate was concentrated and the residue was purified by flash chromatography (silica gel) using 25% ethyl acetate in hexane to afford the desired product (3.5 g, 75%) as a white powder. ¹H-NMR (d₆-DMSO, 400 MHz) δ 9.0 (s, 2H), 3.92 (s, 3H), 2.58 (s, 3H); ES-HRMS m/z 185.041 (M+H C₇H₈N₂O₂S requires 185.0379).

Step 2. Preparation of [2-(methylthio)pyrimidin-5-yl]methanol

To a cold suspension of methyl 2-(methylthio)pyrimidine-5-carboxylate (1.74 g, 9.4 mmol) in dichloromethane (20 mL, −70° C.) was added DIBAL (20.8 mL, 20 mmol) dropwise via an addition funnel. The mixture was stirred under nitrogen at −70° C. for 1 hour and then at −50° C. for 3 hours. The reaction was diluted with dichloromethane (50 mL) and quenched with a suspension of sodium sulfate decahydrate (10 g) in water (50 mL). The slurry was filtered through celite and the filtrate was concentrated. The residue was purified by flash chromatography (silica gel) using 100% ethyl acetate to afford the desired compound (0.7813 g, 39%) as a yellow solid. ¹H-NMR ((CD₃OD, 400 MHz) δ 8.53 (s, 2H), 4.56 (s, 2H), 2.54 (s, 3H); ES-HRMS nz/z 157.0409 (M+H C₆H₈N₂OS requires 157.0430).

Step 3. Preparation of 5-(Chloromethyl)-2-(methylthio)pyrimidine

To a cold solution of [2-(methylthio)pyrimidin-5-yl]methanol (0.7813 g, 5.0 mmol) in anhydrous dichloromethane (10 mL, 0° C.) was added triethylamine (0.836 mL, 8.2 mmol) followed by the addition of methanesulfonyl chloride (0.465 mL, 6.0 mmol). The reaction mixture stirred at 0° C. under a nitrogen atmosphere for 30 minutes then at room temperature for 3.5 hours. The reaction was quenched with sodium bicarbonate (5%, 100 mL)) and extracted with dichloromethane (50 mL). The organic extracts were concentrated and the residue was purified by flash chromatography (silica gel) using 15% ethyl acetate in hexane to afford the desired compound (0.720 g, 82%) as a white solid. ¹H-NMR ((CD₃OD, 400 MHz) δ 8.60 (s, 2H), 4.64 (s, 2H), 2.54 (s, 3H); ES-HRMS m/z 175.0106 (M+H C₆H₇N₂ClS requires 175.0091).

Step 4. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-5-yl]methyl}pyridin-2(1H)-one

To a solution of 5-(Chloromethyl)-2-(methylthio)pyrimidine (0.62 g, 3.56 mmol) in anhdrous DMF (10 mL) was added KBr (0.424, 3.56 mmol). After the suspension stirred at room temperature for 30 minutes, 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (1.05 g, 3.19 mmol) was added followed by NaH (0.102 g, 4.25 mmol). The reaction mixture stirred at 70° C. under a nitrogen atmosphere for 3.5 hours. The solvent was distilled and the residue was washed with water and extracted with ethyl acetate. The organic extracts were concentrated and the residue was purified by reverse phase HPLC using a 10-90% acetonitrile/water (30 minute gradient) at a 70 ml/min flow rate to afford the desired TFA salt (0.32 g, 15%) as a white powder. The TFA compound was washed with sodium bicarbonate (5%) and extracted with dichloromethane. The organic extract was concentrated to afford the desired compound (0.295 g, 18%) as a yellow solid. ¹H-NMR (CD₃OD, 400 MHz) δ 8.47 (s, 2H), 7.62 (q, 1H, J=8 Hz), 7.03 (m, 2H), 6.51 (s, 1H), 5.31 (s, 2H), 5.29 (s, 2H), 2.52 (s, 3H), 2.47 (s, 2H); ES-HRMS m/z 468.0174/470.0156 (M+H C₁₉H₁₆N₃O₂F₂BrS requires 468.0187/470.0168).

Example 708

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-5-yl]methyl}pyridin-2(1H)-one

To a solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-5-yl]methyl}pyridin-2(1H)-one (example 707) (0.26 g, 0.55 mmol) in acetonitrile: water (4:1 v/v, 10 mL) was added MMPP (0.549 g, 1.1 mmol). The reaction stirred at room temperature for 30 hours. The reaction mixture was diluted with ethyl acetate and filtered. The filtrate was concentrated and the residue was purified by reverse phase HPLC using a 10-90% acetonitrile/water (30 minute gradient) at a 70 ml/min flow rate to afford the desired TFA salt of the title copmound (0.13 g, 38%) as a white powder. ¹H-NMR ((CD₃OD, 400 MHz) δ 8.86 (s, 2H), 7.62 (q, 1H, J=8 Hz), 7.02 (m, 2H), 6.56 (s, 1H), 5.48 (s, 2H), 5.31 (s, 2H), 3.34 (s, 3H), 2.49 (s, 2H); ES-HRMS m/z 500.0109/502.0066 (M+H C₁₉H₁₆N₃O₄F₂BrS requires 500.0086/502.0067).

Example 709

Ethyl 2-({[3-bromo-1-(5-{[(2-hydroxyethyl)amino]carbonyl}-2-methylphenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzylcarbamate

To a cooled (−10° C.) solution of 3-[3-bromo-4-[(2-{[(ethoxycarbonyl)amino]methyl}-4-fluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (0.25 g, 0.46 mmol) and 4-methylmorpholine (0.06 mL, 0.55 mmol) in DMF was added isobutyl chloroformate (0.07 mL, 0.55 mmol). The colorless solution gradually turned dark brown. After 30 min, ethaolamine (0.04 mL, 0.69 mmol) was added and the solution warmed to RT. After 1 h, solvent was removed and the crude product was purified by preparatory HPLC. Acetonitrile was evaporated and the solution washed with 5% NaHCO₃ (20 mL) and extracted in DCM (3×15 mL). The organic extracts were dried over Na₂SO₄, filtered, and concentrated to a white solid, dried in vacuo (0.09 g, 33%). ¹H NMR (CD₃OD/400 MHz) δ 7.88 (m, 1H), 7.61 (s, 1H), 7.53 (m, 2H), 7.13 (m, 1H), 7.05 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.43 (s, 2H), 4.07 (q, 2H, J=7.2 Hz), 3.68 (t, 2H, J=5.6 Hz), 3.48 (t, 2H, J=5.6 Hz), 2.09 (s, 3H), 2.00 (s, 3H), 1.22 (t, 3H, J=7.2 Hz). ESHRMS m/z 590.1266 and 592.1254 (M+H calculated for C₂₇H₃₀BrFN₃O₆ requires 590.1297 and 592.1281).

Example 710

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(1H-imidazol-2-yl)-2-methylphenyl]-6-methylpyridin-2(1H)-one Trifluoroacetate

An oven-dried flask was alternately evacuated and flushed with argon. Toluene (2.18 mL) and trimethyl aluminum (1.25 mL, 2.51 mmol) were added sequentially and the solution cooled to −5° C. Ethylene diamine (0.17 mL, 2.51 mmol) was added dropwise. Methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (0.75 g, 1.57 mmol) was added portionwise to the cooled solution. The reaction mixture was then refluxed at 110° C. for 4 h. The solution was cooled and water (0.7 mL), DCM (2.2 mL), and MeOH (2.2 mL) were added. The solution was refluxed for 15 min following this addition and then dried over Na₂SO₄, filtered, and concentrated. The residue was dissolved in EtOAc (20 mL), refluxed 15 min, dried over Na₂SO₄, filtered, and concentrated. The crude product was purified by preparatory HPLC. The product was isolated by freeze-drying and evaporation of the solvent to give a white solid, dried in vacuo (0.30 g, 31%). ¹H NMR (CD₃OD/400 MHz) δ 7.88 (m, 1H), 7.71 (d, 1H, J=8.0 Hz), 7.64 (m, 2H), 7.05 (m, 2H), 6.70 (s, 1H), 5.37 (s, 2H), 4.09 (s, 4H), 2.16 (s, 3H), 2.01 (s, 3H). ESHRMS m/z 488.0750 and 490.0774 (M+H calculated for C₂₃H₂₁BrF₂N₃O₂ requires 488.0780 and 490.0762).

Example 711

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(5-hydroxy-1H-pyrazol-3-yl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

Step 1: Preparation of ethyl 3-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylphenyl}-3-oxopropanoate

In an oven-dried round bottom flask, 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (see Example 487) (0.75 g, 1.62 mmol), DCM (2.00 mL), and oxalyl chloride (0.97 mL, 1.94 mmol) were combined under argon. DMF (3-5 drops) was added to aid in dissolution. Stirred at RT overnight. Solvent was removed and the crude acid chloride was coevaporated with DCM (3-5 mL×3) and dried in vacuo to give an orange solid. In a separate oven-dried flask, in an argon atmosphere, a solution of monoethyl malonate (0.38 mL, 3.23 mmol) in THF (3.00 mL) was cooled to −78° C. Isopropyl magnesium chloride (3.23 mL, 6.46 mmol) was added dropwise. The solution was stirred for 30 min at −78° C. The acid chloride prepared as described above was added dropwise as a solution in THF. The reaction was warmed to RT. After 30 min, the reaction was cooled (0° C.) and 10% citric acid (5.0 mL) added. The crude product was extracted in EtOAc, washed with 5% NaHCO₃, dried over Na₂SO₄, filtered, and concentrated to a crude brown oil. Recrystallization from DCM and hexane. Filtered a beige solid, dried in vacuo (0.41 g, 47%). ¹H NMR (CD₃OD/400 MHz) δ 8.02 (m, 1H), 7.79 (s, 1H), 7.65 (m, 2H), 7.05 (t, 2H, J=9.2 Hz), 6.66 (s, 1H), 5.36 (s, 2H), 4.16 (q, 2H, J=7.2 Hz), 2.11 (s, 3H), 2.07 (s, 2H), 1.99 (s, 3H), 1.23 (t, 3H, J=7.2 Hz). ESHRMS m/z 534.0744 and 536.0746 (M+H calculated for C₂₅H₂₃BrF₂NO₅ requires 534.0722 and 536.0706).

Step 2: Preparation of the Title Compound

To a mixture of ethyl 3-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]4-methylphenyl}-3-oxopropanoate (from Step 1) (0.20 g, 0.37 mmol) in EtOH (5.00 mL) was added hydrazine hydrate (0.01 mL, 0.41 mmol). The reaction mixture was heated at 60° C. with a condensere. After 1 h, additional hydrazine hydrate (0.01 mL) was added. After 2 h, acetic acid (2 drops) was added. At 4 h, additional hydrazine was added (0.1 mL). At 5 h, the reaction appeared to be complete. Left in fridge overnight. Precipitate filtered, washed with hexane, found to be product, a white solid (0.10 g, 54%). ¹H NMR (CD₃OD/400 MHz) δ 7.66 (m, 2H), 7.45 (m, 2H), 7.05 (t, 2H, J=9.6 Hz), 6.65 (s, 1H), 5.36 (s, 2H), 2.04 (s, 3H), 2.02 (s, 3H). ESHRMS m/z 502.0552 and 504.0569 (M+H calculated for C₂₃H₁₉BrF₂N₃O₃ requires 502.0572 and 504.0555).

Example 712

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(5-hydroxyisoxazol-3-yl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

A solution of ethyl 3-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylphenyl}-3-oxopropanoate (0.20 g, 0.37 mmol), triethylamine (0.06 mL, 0.41 mmol), and hydroxylamine hydrochloride (0.03 g, 0.41 mmol) in EtOH (3.00 mL) was heated overnight at 60° C. with a condenser. Additional triethylamine (0.06 mL) and hydroxylamine hydrochloride (0.03 g) were added. After 2.5 h, the additions of triethylamine and hydroxylamine hydrochloride were repeated. After 1 h, the reaction was concentrated and purified by preparatory HPLC. The product was isolated by freeze-drying and evaporation of the solvent to give a white solid. Dissolved solid in DCM. Upon addition of 5% NaHCO₃, solution became a milky emulsion. Added additional DCM and some brine. Organic extracts were dried over Na₂SO₄, filtered, and concentrated to a pink solid, dried in vacuo (120 mg, 64%). ¹H NMR (CD₃OD/400 MHz) δ 7.66 (m, 2H), 7.44 (m, 2H), 7.04 (t, 2H, J=8.8 Hz), 6.64 (s, 1H), 5.36 (s, 2H), 2.04 (s, 3H), 2.01 (s, 3H). ESHRMS m/z 503.0415 and 505.0402 (M+H calculated for C₂₃H₁₈BrF₂N₂O₄ requires 503.0413 and 505.0395).

Example 713

3-[4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

To a cooled (−15° C.) solution of 3-[4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (see Example 651) (0.30 g, 0.63 mmol) and isobutyl chloroformate (0.10 mL, 0.75 mmol) in DMF (3.00 mL) was added 4-methylmorpholine (0.08 mL, 0.75 mmol). The solution instantly turned yellow and was dark brown within minutes. After 20 min, methylamine (0.47 mL of 2.0M solution in THF, 0.94 mmol) was added. The reaction was carried out at RT. After 2.5 h, a catalytic amount of DMAP and additional methylamine (0.47 mL, 0.94 mmol) were added. After an additional 2.5 h, the reaction was concentrated to a dark red oil. The crude product was purified by preparatory HPLC. Acetonitrile was evaporated and the solution washed with 5% NaHCO₃ (20 mL) and extracted in DCM (3×15 mL). The organic extracts were dried over Na₂SO₄, filtered, and concentrated to an off-white solid, dried in vacuo (0.06 g, 19%). ¹H NMR (CD₃OD/400 MHz) δ 7.85 (m, 1H), 7.58 (s, 1H), 7.48 (m, 2H), 7.14 (m, 1H), 7.02 (m, 1H), 6.23 (s, 1H), 6.09 (s, 1H), 5.20 (s, 2H), 4.45 (s, 2H), 2.90 (s, 3H), 2.49 (m, 1H), 2.11 (s, 3H), 1.91 (s, 3H), 0.71 (m, 2H), 0.48 (m, 2H). ESHRMS ff/z 493.2260 (M+H calculated for C₂₇H₃₀N₄O₄F requires 493.2246).

Example 714

Methyl 4-{[4-[(2,4-difluorobenzyl)oxy]-2-oxoquinolin-1(2H)-yl]methyl}benzoate

Step 1: Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]quinolin-2(1H)-one.

To a room temperature solution of 4-hydroxy-1,2-dihydroquinolin-2-one (500 mg, 3.10 mmol) in CH₂Cl₂ (10.0 mL) was added portion-wise solid N-bromosuccinimide (551.5 mg, 3.10 mmol). The reaction was stirred vigorously for 1.0 h, followed by the sequential addition of K₂CO₃ (540 mg, 3.90 mmol), DMF (4.0 mL), and 2,4 difluorobenzyl bromide (0.430 mL, 3.30 mmol). The resulting suspension was stirred for 4.5 hours until complete formation of desired product was seen by LCMS analysis. The reaction was then diluted with ethyl acetate (400 mL) and brine washed (3×200 mL). The resulting organic extract was Na₂SO₄ dried, filtered, and concentrated in vacuo to a residue that was subjected to SiO₂ chromatography with ethyl acetate/hexanes/methanol (60:35:5) to furnish a solid (529 mg, 47%). ¹H NMR (300 MHz, d₆-DMSO) δ 12.23 (s, 1H), 7.68 (app q, J=7.5 Hz, 1H), 7.64 (app q, J=8.5 Hz, 1H), 7.54 (app q, J=8.3 Hz, 1H), 7.38-7.27 (m, 2H), 7.20 (app t, J=7.4 Hz, 1H), 7.13 (app dt, J=8.4, 2.6 Hz, 1H), 5.25 (s, 2H); LC/MS C-18 column, t_r=2.64 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 366 (M+H). ES-HRMS m/z 365.9967 (M+H calcd for C₁₆H, BrF₂NO₂ requires 365.9936).

Step 2: Preparation of Methyl 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxoquinolin-1(2H)-yl]methyl}benzoate

To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]quinolin-2(1H)-one (400 mg, 1.09 mmol) in THF (4.5 mL) was added portion-wise solid sodium hydride (95% oil-free, 60.0 mg, 2.49 mmol). The reaction was vigorously stirred for 30 minutes followed by addition of methyl-4-(bromomethyl)-benzoate (400 mg, 1.75 mmol). This resulting suspension was then heated to 60° C. for 12.0 hours. The resulting solution was then treated with saturated aqueous ammonium chloride (400 mL) and extracted with ethyl acetate (3×300 mL). The resulting organic extracts were Na₂SO₄ dried, filtered, and concentrated in vacuo to a residue that was subjected to SiO₂ chromatography with ethyl acetate/hexanes (60:40) to furnish a solid (396 mg, 71%). ¹H NMR (400 MHz, CDCl₃) δ 7.97 (app d, J=8.0 Hz, 2H), 7.87 (d, J=7.5 Hz, 1H), 7.60 (app q, J=8.4 Hz, 1H), 7.49-7.42 (m, 1H), 7.30-7.15 (m, 4H), 6.94 (app t, J=6.3 Hz, 1H), 6.88 (app t, J=9.4 Hz, 1H), 5.64 (s, 2H), 5.33 (s, 2H), 3.88 (s, 3H); LC/MS C-18 column, t_r=3.46 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 514 (M+H). ES-HRMS m/z 514.0451 (M+H calcd for C₂₅H₁₉BrF₂NO₄ requires 514.0460).

Step 3: Preparation of the title compound. In a 25 mL round bottom flask was added, at room temperature, a solution of methyl 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxoquinolin-1(2H)-yl]methyl}benzoate (step 2) (120 mg, 0.233 mmol) in MeOH (3.0 mL). Next, a combination of Pd on carbon (10% Pd, weight by weight 50% water, 100 mg, 0.047 mmol) and Pd(OAc)₂ (15 mg, 0.067 mmol) was added to the reaction vessel that purged with argon and then fitted with a septum. The vessel was then equipped with a 2.0 L hydrogen balloon (c.a. 20 psi). The resulting suspension was allowed to stir of 12.0 hours and was then directly applied to SiO₂ chromatography using ethyl acetate/hexanes (3:7) to furnish the desired title compound as a solid (52 mg, 51%). ¹H NMR (300 MHz, CDCl₃) δ 8.05-7.98 (m, 3H), 7.55 (app q, J=8.3 Hz, 1H), 7.48 (app t, J=7.5 Hz, 1H), 7.30 (d, J=8.0 Hz 2H), 7.19 (app q, J=8.5, 2H), 7.05-6.90 (m, 2H), 6.28 (s, 1H), 5.60 (s, 2H), 5.26 (s, 2H), 3.91 (s, 3H); LC/MS C-18 column, t_r=3.71 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 436 (M+H). ES-HRMS m/z 436.1371 (M+H calcd for C₂₅H₂₀BrF₂NO₄ requires 436.1355).

Example 715

5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furamide

Step 1: Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furoic Acid

To a room temperature solution of methyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furoate (Example 660) (608 g, 1.30 mmol) in THF (8.0 mL) was added dropwise an aqueous solution of sodium hydroxide (3.0 M, 0.50 mL, 1.50 mmol). The reaction was then heated to 60° C. for 12.0 hours. The resulting suspension was then diluted with 500 mL of ethyl acetate and neutralized with an aqueous solution of hydrochloric acid (1.0 N, 1.5 mL, 10 mmol). The resulting biphasic solution was then concentrated in vacuo to a volume of 50 mL. At this time a white solid began to form and the resulting solid suspension was allowed to sit until precipitation appeared to stop (approximately 1.0 hour). The precipitate was collected and dried in vacuo (1.0 mm Hg) to furnish the solid acid as an intermediate (500 mg, 85%). ¹H NMR (300 MHz, d₄-MeOH) δ 7.64 (app q, J=8.3 Hz, 1H), 7.18 (d, J=3.4 Hz, 1H), 7.10-7.02 (m, 2H), 6.54 (s, 1H), 6.50 (d, J=3.5 Hz, 1H), 5.42 (s, 2H), 5.37 (s, 2H), 2.64 (s, 3H); LC/MS C-18 column, t_r=2.38 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 454 (M+H). ES-HRMS m/z 454.0070 (M+H calcd for C₁₉H₁₅BrF₂NO₅ requires 454.0096).

Step 2: Preparation of the title compound. To a room temperature suspension of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furoic acid (500 mg, 1.10 mmol) in THF (6.0 mL) was added 2-chloro-4,6 dimethoxy-1,3,5 triazine (307 mg, 1.75 mmol) and N-methyl morpholine (NMM, 184 mg, 1.82 mmol) sequentially. The resulting solution was matured for 2 hours and then a saturated aqueous solution of ammonium hydroxide (0.70 mL) was added. The resulting suspension was allowed to continue for 1 additional hour. The reaction mixture was diluted with 400 mL of brine and extracted with ethyl acetate (3×400 mL). The organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo and the resulting residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes/methanol (57:38:5) to provide the title compound (370 mg, 74%). ¹H NMR (300 MHz, d₄-MeOH) δ 7.64 (app q, J=8.1 Hz, 1H), 7.10-7.00 (m, 3H), 6.53 (s, 1H), 6.52 (d, J=3.4 Hz, 1H), 5.43 (s, 2H), 5.32 (s, 2H), 2.61 (s, 3H); LC/MS C-18 column, t_r=2.15 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 453 (M+H). ES-HRMS m/z 453.0249 (M+H calcd for C₁₉H₁₆BrF₂N₂O₄ requires 453.0256).

Example 716

5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furamide

Step 1: Preparation of Methyl 5-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-2-furoate

To a room temperature solution of methyl-2-amino-5-furoate (4.85 g, 34.4 mmol) in 1,4 dioxane (28.0 mL) was added 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione (8.16 g, 44.3 mmol). The reaction was stirred vigorously and heated quickly (within 8 minutes) to an internal temperature of 98° C. Upon reaching temperature, the reaction was maintained for 1.0 hour. At this time, the reaction was cooled to room temperature rapidly using an ice-bath and methane sulfonic acid (3.30 g, 34.4 mmol) was added. The reaction mixture was once again brought to an internal temperature of approximately 100° C. After 1.0 hour the reaction was diluted with 10 mL of toluene and allowed to cool to room temperature on its own accord. A solid formed after 3.0 hours that was collected and subsequently recrystallized from methanol/ethyl acetate (1:1). The developing crystals were allowed to form and stand for 12.0 hours prior to collection to furnish the desired product as a solid (3.78 g, 44%). ¹H NMR (400 MHz, d₇-DMF) δ 11.34 (s, 1H), 7.43 (app d, J=3.6 Hz, 1H), 6.79 (app d, J=3.6 Hz, 1H), 6.01 (s, 1H), 5.63 (d, J=2.0 Hz, 1H), 3.87 (s, 3H), 2.02 (s, 3H); LC/MS C-18 column, t_r=1.47 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 250 (M+H). ES-HRMS nz/z 250.0696 (M+H calcd for C₁₂H₁₂NO₅ requires 250.0710).

Step 2: Preparation of Methyl 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furoate

To a room temperature solution of methyl 5-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)-2-furoate (step 1) (3.19 g, 12.8 mmol) in DMF (14 mL) was added portion-wise solid N-bromosuccinimide (2.29 g, 12.9 mmol). The reaction was stirred vigorously for 1.0 h, followed by the sequential addition of K₂CO₃ (1.88 g, 13.6 mmol), DMF (4.0 mL), and 2,4 difluorobenzyl bromide (2.00 mL, 15.55 mmol). The resulting suspension was stirred for 9.0 hours until complete formation of desired product was seen by LCMS analysis. The reaction was then diluted with saturated brine (300 mL) and extracted with ethyl acetate (3×300 mL). The resulting organic extracts were Na₂SO₄ dried, filtered, and concentrated in vacuo to a residue that was subjected to SiO₂ chromatography with a gradient elution using ethyl acetate/hexanes (40:60 to 60:40) to furnish a solid (3.20 mg, 55%). ¹H NMR (400 MHz, d₇-DMF) δ 7.78 (app q, J=8.6 Hz, 1H), 7.48 (app d, J=3.6 Hz, 1H), 7.33 (app dt, J=10.0, 2.4 Hz, 1H), 7.21 (app dt, J=8.5, 1.8 Hz, 1H), 6.92 (d, J=3.6 Hz, 1H), 6.81 (s, 1H), 5.47 (s, 2H), 3.88 (s, 3H), 2.15 (s, 3H); LC/MS C-18 column, t_r=3.11 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 m/min with detection 254 nm, at 50° C.). ES-MS m/z 454 (M+H). ES-HRMS m/z 454.0117 (M+H calcd for C₁₉H₁₅BrF₂N₂O₅ requires 454.0096).

Step 3: 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furoic Acid

To a room temperature solution of methyl 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furoate (step 2) (3.00 g, 6.61 mmol) in THF (20 mL) was added dropwise an aqueous solution of sodium hydroxide (3.0 M, 4.00 mL, 12.0 mmol). The reaction was then heated to 60° C. for 12.0 hours. The resulting suspension was then diluted with 800 mL of ethyl acetate and neutralized with an aqueous solution of hydrochloric acid (3.0 N, 4.0 mL, 12 mmol). The resulting biphasic solution was then concentrated in vacuo to a volume of 90 mL. At this time a white solid began to form and the resulting solid suspension was allowed to sit until precipitation appeared to stop (approximately 1.0 hour). The precipitate was collected and dried in vacuo (1.0 mm Hg) to furnish the solid acid as an intermediate (2.27 g, 78%). ¹H NMR (400 MHz, d₇-DMF) δ 7.79 (app q, J=8.0 Hz, 1H), 7.32 (t, J=9.2 Hz, 1H), 7.20 (app t, J=7.4 Hz, 1H), 6.88 (app d, J=2.5 Hz, 1H), 6.74 (s, 1H), 6.51 (d, J=2.5 Hz, 1H), 5.44 (s, 2H), 2.10 (s, 3H); LC/MS C-18 column, t_r=2.77 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 440 (M+H). ES-HRMS m/z 439.9959 (M+H calcd for C₁₈H₁₃BrF₂NO₅ requires 439.9940).

Step 4: Preparation of the Title Compound

To a room temperature suspension of 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furoic acid (1.00 g, 2.27 mmol) in THF (8.0 mL) was added 2-chloro-4,6 dimethoxy-1,3,5 triazine (610 mg, 3.47 mmol) and N-methyl morpholine (NMM, 368 mg, 3.62 mmol) sequentially. The resulting solution was matured for 2 hours and then a saturated aqueous solution of ammonium hydroxide (1.5 mL) was added. The resulting suspension was allowed to continue for 1 additional hour. The reaction mixture was diluted with 800 mL of brine and extracted with ethyl acetate (3×600 mL). The organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo and the resulting residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes/methanol (57:38:5) to provide the title compound (710 mg, 71%). ¹H NMR (400 MHz, d₇-DMF) δ 8.07 (s, 1H), 7.79 (app q, J=8.6 Hz, 1H), 7.50 (br s, 1H), 7.32 (app dt, J=10.1, 2.2 Hz, 1H), 7.30 (app dd, J=8.0, 3.3 Hz, 1H), 7.20 (app dt, J=8.6, 2.0 Hz, 1H), 6.81 (s, 1H), 6.79 (d, J=3.4 Hz, 1H), 5.47 (s, 2H), 2.14 (s, 3H); LC/MS C-18 column, t_r=2.60 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 439 (M+H). ES-HRMS m/z 439.0088 (M+H calcd for C₁₈H₁₄BrF₂N₂O₄ requires 439.0010).

Example 717

1-[3,5-bis(hydroxymethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1: Preparation of Dimethyl 5-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)isophthalate

Dimethyl 5-aminoisophthalate (24.45 g, 117 mmol) was dissolved in 500 ml toluene and heated to reflux. 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione (40.0 g, 175.3 mmol) was added and refluxed for 15 minutes. The reaction was evaporated. 500 ml of acetonitrile and p-toluenesulphonic acid (22.25 g, 117 mmol) was added and refluxed for 1 hour. The reaction was allowed to cool to room temperature and stand over night. The resulting precipitate was filtered, washed three times with 250 ml water and 250 ml acetonitrile and dried in vacuo to give a tan solid (18.85 g, 51% yield). ¹H NMR (300 MHz, DMSO-d₆) δ 10.70 (br s, 1H), 8.47 (t, J=1.54 Hz, 1H), 7.99 (d, J=1.47 Hz, 2H), 5.90 (d, J=1.61 Hz, 1H), 5.55 (d, J=2.42 Hz, 1H), 3.87 (s, 6H), 1.82 (s, 3H); LC/MS, t_r=1.79 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 318 (M+H). ES-HRMS m/z 318.0994 (M+H calcd for C₁₆H₁₆NO₆ requires 318.0972).

Step 2: Preparation of Dimethyl 5-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)isophthalate

Dimethyl-5-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)isophthalate from Step 1) (18.0 g, 56.7 mmol) was stirred at room temperature with N-Bromosuccinimide (10.6 g, 59.6 mmol) in 35 ml of N,N-dimethylformamide and 180 ml of methylene chloride. After stirring for 1 hour, a white precipitate had formed. The precipitate was filtered, washed with acetonitrile and dried in vacuo to give a white solid (11.55 g, 51%). ¹H NMR (400 MHz, DMSO-d₆) δ 11.49 (br s, 1H), 8.49 (t, J=1.24 Hz, 1H), 8.06 (d, J=1.47 Hz, 2H), 6.07 (s, 1H), 3.88 (s, 6H), 1.82 (s, 3H); LC/MS, t_r=1.81 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 396 (M+H). ES-HRMS m/z 396.0102 (M+H calcd for C₁₆H₁₅BrNO₆ requires 396.0077).

Step 3: Preparation of Dimethyl 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalate

Dimethyl 5-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)isophthalate from Step 2) (11.3 g, 28.5 mmol) was stirred briskly with 2,4-difluorobenzylbromide (3.66 ml, 28.5 mmol) and K₂CO₃ (5.91 g, 42.8 mmol) in 50 ml of N,N-dimethylformamide at room temperature for 3 hours. The reaction was then poured into 1 L of cold water and the resulting precipitate was filtered, washed with water and diethyl ether, and dried in vacuo to yield a white solid (13.8 g, 93%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.51 (t, J=1.60 Hz, 1H), 8.12, (d, J=1.60 Hz, 2H), 7.67 (app q, J=7.92 Hz, 1H), 7.34 (app dt, J=9.94, 2.19 Hz, 1H), 7.17 (dt, J=8.53, 2.11 Hz, 1H), 6.68 (s, 1H), 5.33 (s, 2H), 3.88 (s, 6H), 1.93 (s, 3H); LC/MS, t_r=2.77 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS nm/z 522 (M+H). ES-HR/MS nm/z 522.0335 (M+H calcd for C₂₃H₁₉BrF₂NO₆ requires 522.0358).

Step 4: Preparation of 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalic Acid

Dimethyl 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalate from Step 3) (5.0 g, 9.57 mmol) was stirred at room temperature with 2.5 N NaOH (15.3 ml, 38.3 mmol) in 30 ml of 5:1 THF/water for 1 hour. The reaction was then acidified with 1 N HCl and the resulting precipitate was filtered, washed with water, and dried in vacuo to yield a white solid (4.48 g, 95%). ¹H NMR (400 MHz, DMSO-d₆) δ 13.50 (br s, 2H), 8.51 (t, J=1.41 Hz, 1H), 8.02, (d, J=1.48 Hz, 2H), 7.67 (app q, J=7.88 Hz, 1H), 7.32 (dt, J=9.94, 2.19 Hz, 1H), 7.16 (dt, J=8.52, 1.99 Hz, 1H), 6.68 (s, 1H), 5.32 (s, 2H), 1.94 (s, 3H); LC/MS, t_r=2.27 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 494 (M+H). ES-HRMS m/z 494.0054 (M+H calcd for C₂₁H₁₅BrF₂NO₆ requires 494.0045).

Step 5: Preparation of the title compound. 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalic acid from Step 4 above) (500 mg, 1.01 mmol) was added to a solution of 1M borane-dimethylsulfide complex in tetrahydrofuran (9.0 ml, 9.00 mmol) in 2.5 ml tetrahydrofuran at 0° C. The reaction was allowed to warm to room temperature while stirring. After stirring overnight, more 1M borane-dimethylsulfide complex in tetrahydrofuran (0.60 ml, 0.60 mmol) was added and stirring at room temperature. After 4 hours, ice chips were added to quench the reaction. The reaction was extracted 2 times with ethyl acetate and the combined organic layers were washed with brine, dried over MgSO₄ and evaporated. The resulting solid was washed with acetonitrile and diethyl ether and dried in vacuo to give a white solid (281 mg, 60%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.66 (app q, J=7.92 Hz, 1H), 7.35 (s, 1H), 7.33 (dt, J=9.40, 2.24 Hz, 1H), 7.16 (dt, J=8.52, 1.88 Hz, 1H), 6.99 (s, 2H), 6.62 (s, 1H), 5.31 (s, 2H), 5.27 (br s, 2H), 4.51 (s, 4H), 1.93 (s, 3H); LC/MS, t_r=2.19 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 466 (M+H). ES-HRMS m/z 466.0454 (M+H calcd for C₂₁H₁₉BrF₂NO₄ requires 466.0460).

Example 718

5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalamide

5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalic acid (Example 717, step 4) (500 mg, 1.01 mmol) was dissolved in 4 ml of tetrahydrofuran. 0.5M ammonia in 1,4-dioxane (12.12 ml, 6.06 mmol) was added, followed, in order, by EDCI (494 mg, 2.53 mmol), 1-hydroxybenzotriazole (342 mg, 2.53 mmol) and triethylamine (563 μl, 4.04 mmol). The reaction was stirred at room temperature overnight. The reaction evaporated and water was used to triturate the product. The resulting solid was filtered and washed with water, acetonitrile, ethyl acetate and diethyl ether, and dried in vacuo to give a white solid (202 mg, 41%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.45 (s, 1H), 8.08 (br s, 2H), 7.86, (d, J=1.34 Hz, 2H), 7.67 (app q, J=7.92 Hz, 1H), 7.55 (br s, 2H), 7.33 (dt, J=9.94, 2.18 Hz, 1H), 7.17 (dt, J=8.59, 1.92 Hz, 1H), 6.70 (s, 1H), 5.34 (s, 2H), 1.96 (s, 3H); LC/MS, t_r=2.10 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 492 (M+H). ES-HRMS m/z 492.0381 (M+H calcd for C₂₁H₁₇BrF₂N₃O₄ requires 492.0365).

Example 719

1-[3,5-bis(1-hydroxy-1-methylethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Dimethyl 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalate (Example 717, step 3) (500 mg, 0.96 mmol) was added dropwise to a solution of 3M MeMgBr in diethyl ether (1.6 ml, 4.79 mmol) in 15 ml of tetrahydrofuran at −5° C. and stirred at −5° C. The reaction turned red. After 2.5 hours, the reaction was quenched with a saturated NH₄Cl solution and extracted 2 times with ethyl acetate. The combined organic layers were washed with NaHCO₃ solution and brine, dried over MgSO₄ and evaporated. The resulting solid was washed with diethyl ether and dried in vacuo to give a white solid (329 mg, 66%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.69-7.63 (m, 2H), 7.33 (dt, J=9.87, 2.41 Hz, 1H), 7.16 (dt, J=8.46, 1.75 Hz, 1H), 7.07 (d, J=1.48 Hz, 2H), 6.61 (s, 1H), 5.32 (s, 2H), 5.06 (s, 2H), 1.89 (s, 3H), 1.41 (s, 12H); LC/MS, t_r=2.45 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 522 (M+H). ES-HRMS m/z 522.1098 (M+H calcd for C₂₅H₂₇BrF₂NO₄ requires 522.1086).

Example 720

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic acid (Example 203) (500 mg, 1.11 mmol) was added to a solution of 2M borane-dimethylsulfide complex in tetrahydrofuran (3.33 ml, 6.66 mmol) in 2.5 ml tetrahydrofuran at 0° C. The reaction was allowed to warm to room temperature while stirring. After 2.5 hours, ice chips were added to quench the reaction. The resulting precipitate was filtered, washed with diethyl ether and dried in vacuo to give a white solid (160 mg, 33%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.66 (app q, J=7.88 Hz, 1H), 7.42 (d, J=8.19 Hz, 2H), 7.33 (dt, J=9.87, 2.06 Hz, 1H), 7.19-7.14 (m, 3H), 6.62 (s, 1H), 5.31 (s, 2H), 5.30 (s, 1H), 4.54 (d, J=5.24, 2H), 1.92 (s, 3H); LC/MS, t_r=2.36 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 436 (M+H). ES-HRMS m/z 436.0374 (M+H calcd for C₂₀H₁₇BrF₂NO₃ requires 436.0354).

Example 721

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1-hydroxy-1-methylethyl)phenyl]-6-methylpyridin-2(1H)-one

Methyl-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (Example 202) (500 mg, 1.08 mmol) was added dropwise to a solution of 3M MeMgBr in diethyl ether (0.90 ml, 2.69 mmol) in 15 ml of tetrahydrofuran at −5° C. and stirred at −5° C. After 2.75 hours, more 3M MeMgBr in diethyl ether (0.45 ml, 1.35 mmol) was added and stirred at −5° C. After 4 hours, the reaction was quenched with a saturated NH₄Cl solution and extracted 2 times with ethyl acetate. The combined organic layers were washed with NaHCO₃ solution and brine, dried over MgSO₄ and evaporated. The resulting solid was washed with diethyl ether and dried in vacuo to give a white solid (268 mg, 53%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.66 (app q, J=7.92 Hz, 1H), 7.57 (d, J=8.46 Hz, 2H), 7.33 (dt, J=9.87, 2.11 Hz, 1H), 7.16 (dt, J=8.59, 2.24 Hz, 1H), 7.14 (d, J=8.63 Hz, 2H), 6.62 (s, 1H), 5.31 (s, 2H), 5.12 (s, 1H), 1.91 (s, 3H), 1.44 (s, 6H); LC/MS, t_r=2.54 minutes (5 to 95% acetonitrile/water over 5 minutes at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 464 (M+H). ES-HRMS m/z 464.0604 (M+H calcd for C₂₂H₂₁BrF₂NO₃ requires 464.0667).

Example 722

1-(5-amino-2-fluorophenyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Hydrochloride

Step 1 Preparation of Tert-Butyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenylcarbamate

A solution of the compound of Example 519 (4.3 g, 9.2 mmol) in tert-butanol (50 mL) was flushed with nitrogen. Diphenyl phosphoryl azide (2 mL, 9.2 mmol) and triethyl amine (1.3 mL, 9.2 mmol) were added. After heating at 90 C for 20 h, the reaction mixture was concentrated in vacuo. The residue was diluted with methylene chloride and was washed sequentially with aqueous ammonium chloride and aqueous NaHCO₃. The organic layer was concentrated in vacuo; the resulting solids were suspended in acetonitrile and filtered to give the title compound (2.9 g, 58%). ¹H NMR (400 MHz, CD₃OD) δ 7.64 (q, J=7.2 and 14.4 Hz, 1H), 7.49 (m, 1H), 7.43 (m, 1H), 7.24 (t, J=9.6 Hz, 1H), 7.04 (t, J=8.4 Hz, 2H), 6.62 (s, 1H), 5.35 (s, 2H), 2.09 (s, 3H), 1.49 (s, 9H) ppm. ¹⁹F NMR (300 MHz, CD₃OD) δ −111.53 (1F), −115.93 (1 F), −132.58 ppm. ES-HRMS m/z 540.0822 (M+H calcd for C₂₄H₂₃BrF₃N₂O₄ requires 540.0820).

Step 2 Preparation of 1-(5-amino-2-fluorophenyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Hydrochloride

The product of Step 1(2.9 g, 5.3 mmol) was dissolved in tetrahydrofuran (75 mL) and 6N HCl (10 mL). The reaction mixture was heated at 60 C for 18 h and was concentrated in vacuo to give the final product (1.89 g, 75%). ¹H NMR (400 MHz, CD₃OD) δ 7.64 (q, J=8.4 and 15.2 Hz, 1H), 7.56 (m, 2H), 7.46 (m, 1H), 7.05 (m, 2H), 6.69 (s, 1H), 5.37 (s, 2H), 2.10 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.37 (1F), −115.86 (1 F), −123.16 ppm. ES-HRMS m/z 440.0334 (M+H calcd for C₁₉H₁₅BrF₃N₂O₂ requires 440.0295).

Example 723

N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}-2-hydroxyacetamide

Step 1 Preparation of 2-({3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}amino)-2-oxoethyl Acetate

A solution of the compound of Example 722 (0.5 g, 1.05 mmol) in tetrahydrofuran (20 mL) was treated with triethyl amine (0.3 mL, 2.1 mmol) and acetoxy acetylchloride (0.12 mL, 1.15 mmol). After stirring at room temperature for 2 h, the reaction was complete. The reaction mixture was poured into saturated aqueous ammonium chloride. The solids were filtered off and were washed with water and diethyl ether. Title product was isolated as a white solid (0.32 g, 58%). ¹H NMR (400 MHz, CD₃OD) δ 7.65 (m, 3H), 7.32 (t, J=8.4 Hz, 1H), 7.04 (t, J=8.4 Hz, 2H), 6.64 (s, 1H), 5.35 (s, 2H), 4.68 (s, 2H), 2.15 (s, 3H), 2.10 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.56 (1F), −115.99(1 F), −129.48 (1F) ppm. LC/MS, t_r=5.35 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 540 (M+H).

Step 2 Preparation of N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}-2-hydroxyacetamide

The product of Step 1(0.1 g, 0.18 mmol) was suspended in tetrahydrofuran (10 mL), methanol (2 mL), and 2.5 N NaOH (1 mL). After stirring at room temperature for 1 hour, the reaction was complete and the organics were removed in vacuo. The aqueous layer was acidified to pH 1 with 6N HCl, the solids were suspended in water, filtered, and washed with diethyl ether. The title compound, was obtained as a white powder (56.2 mg, 61%). ¹H NMR (400 MHz, CD₃OD) δ 7.75 (dq, J=2.9, 4.8 and 9.2 Hz, 1H), 7.71 (dd, J=2.4 and 6.8 Hz, 1H), 7.64 (q, J=8 and 14.8 Hz, 1H), 7.32 (t, J=9.6 Hz, 1H), 7.04 (t, J=8.8 Hz, 2H), 6.64 (s, 1H), 5.36 (s, 2H), 4.10 (s, 2H), 2.10 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.54 (1F), −115.99 (1 F), −129.71 (1F) ppm. LC/MS, t_r=5.04 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 498 (M+H).

Example 724

N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}-2-hydroxy-2-methylpropanamide

Step 1 Preparation of 2-({3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}amino)-1,1-dimethyl-2-oxoethyl Acetate

A solution of the compound of Example 722 (0.5 g, 1.05 mmol) in tetrahydrofuran (20 mL) was treated with triethyl amine (0.3 mL, 2.1 mmol) and 1-chlorocarbonyl-1-methylethyl acetate (0.16 mL, 1.15 mmol). After stirring at room temperature for 2 h, the reaction was complete. The reaction mixture was poured into saturated aqueous ammonium chloride. The solids were filtered off and were washed with water and diethyl ether. The compound of Step 1 was isolated as a white solid (0.23 g, 39%). ¹H NMR (400 MHz, CD₃OD) δ 7.64 (m, 2H), 7.54 (dd, J=2.8 and 6.8 Hz, 1H), 7.30 (t, J=9.2 Hz, 1H), 7.04 (t, J=9.2 Hz, 2H), 6.64 (s, 1H), 5.35 (s, 2H), 2.11 (s, 3H), 2.08 (s, 3H), 1.61 (s, 6H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.57 (1F), −116.00 (1 F), −129.56 (1F) ppm. LC/MS, t_r=5.65 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 568 (M+H).

Step 2 Preparation of N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}-2-hydroxy-2-methylpropanamide

The product of Step 1(0.1 g, 0.17 mmol) was suspended in tetrahydrofuran (10 mL), methanol (2 mL), and 2.5 N NaOH (1 mL). After stirring at room temperature for 1 hour, the reaction was complete and the organics were removed in vacuo. The aqueous layer was acidified to pH 1 with 6N HCl, the solids were suspended in water, filtered, and washed with diethyl ether. The title compound was obtained as a white powder (56 mg, 61%). ¹H NMR (400 MHz, CD₃OD) δ 7.75 (dq, J=2.8, 4.4 and 9.2 Hz, 1H), 7.69 (dd, J=2.8 and 6.8 Hz, 1H), 7.64 (q, J=8 and 14.8 Hz, 1H), 7.31 (t, J=9.2 Hz, 1H), 7.04 (t, J=8.4 Hz, 2H), 6.64 (s, 1H), 5.35 (s, 2H), 2.10 (s, 3H), 1.43 (s, 6H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.55 (1F), −115.95 (1 F), −129.80 (1F) ppm. LC/MS, t_r=5.34 minutes (5 to 95% acetonitrile/water over 8 minutes at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 526 (M+H).

Example 725

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluoro-N,N-dimethylbenzamide

Step 1 Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzoic Acid

The compound of Example 604 (4.1 g, 8.5 mmol) was suspended in tetrahydrofuran (30 mL), methanol (15 mL), water (15 mL) and 2.5 N NaOH (6.8 mL, 17 mmol)). After stirring at room temperature for 2 hour, the reaction was complete and the organics were removed. The aqueous layer was acidified to pH 1 with 3N HCl, the solids were suspended in water, filtered, and washed with diethyl ether. The title compound was obtained as a white powder and used without further purification (4.4 g). ¹H NMR (400 MHz, CD₃OD) δ 8.00 (dd, J=1.8 and 8.8 Hz, 1H), 7.93 (dd, J=1.48 and 10 Hz, 1H), 7.64 (q, J=8 and 14.8 Hz, 1H), 7.49 (t, J=7.6 Hz, 1H), 7.05 (t, J=10 Hz, 2H), 6.66 (s, 1H), 5.36 (s, 2H), 2.08 (s, 3H) ppm. ¹⁹F NMR (400 MHz, CD₃OD) δ −111.48 (1F), −115.96 (1 F), −123.35 (1F) ppm. ES-HRMS m/z 468.9987 (M+H calcd for C₂₀H₁₄BrF₃NO₄ requires 469.0086).

Step 2 Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluoro-N,N-dimethylbenzamide

A solution of the product of Step 1(0.5 g, 1.07 mmol) in N,N-dimethyl formamide was cooled to 0 C. Iso-butyl chloroformate (0.14 mL, 1.07 mmol) and N-methyl morpholine (0.12 mL, 1.07 mmol) were added. After 20 minutes, N,N-dimethylamine (2.0 M, 1.1 mL, 2.14 mmol) was added and the reaction mixture was warmed to room temperature over 18 h. The reaction mixture was partitioned between ethyl acetate and saturated aqueous NaHCO₃. The organics were washed with brine and concentrated in vacuo. The resulting semi-solid was treated with ethyl acetate and acetone to precipitate the title compound (90 mg, 17%). ¹H NMR (400 MHz, dmso-d₆) δ 7.67 (q, J=8 and 14.8 Hz, 1H), 7.52 (m, 2H), 7.35 (m, 2H), 7.18 (td, J=2.8 and 8.8 Hz, 1H), 6.73 (s, 1H), 5.34 (s, 2H), 2.98 (s, 3H), 2.91 (s, 3H), 2.00 (s, 3H) ppm. ¹⁹F NMR (400 MHz, dmso-d₆) δ −109.50 (1F), −113.63 (1 F), −122.09 (1F) ppm. ES-HRMS m/z 496.0570 (M+H calcd for C₂₂H₁₉BrF₃N₂O₃ requires 496.0558).

Example 726

3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(1-glycoloyl-2,3-dihydro-1H-indol-5-yl)methyl]-6-methylpyridin-2(1H)-one

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with compound of Example 633 (180 mg, 0.43 mmol), acetoxyacetyl chloride (51 μL, 0.47 mmol), triethylamine (119 μL, 0.86 mmol) and tetrahydrofuran (3.0 mL). After stirring at 25° C. for 20 min the reaction was completed by LC-MS. NaOH (2.5M, 2.24 mmol, 1.0 mL) and MeOH (2.0 mL) was added and stirred for 20 min to give the title compound. The compound precipitated out of solution. The precipitated was filtered and washed with water and diethyl ether to obtain the title compound (130 mg, 64%) as a white solid. ¹H NMR (400 MHz, (DMSO) δ 7.9 (d, J=8.2, 1H), 7.6 (q, J=8.5 and 6.9 Hz, 1H), 7.3 (t, J=8.7 Hz, 1H), 7.1 (t, J=7.9 Hz, 1H), 6.9 (s, 2H), 6.5 (s, 1H), 5.25 (s, 2H), 4.1 (d, J=5.5 Hz, 2H), 3.9 (t, J=8.6 Hz, 2H), 3.42 (t, J=5.4 Hz, 1H), 3.35 (t, J=4.8 Hz, 1H), 3.2 (t, J=8.5 Hz, 2H), 2.3 (s, 3H) ppm. ES-HRMS m/z 475.1220 (M+H calcd for C₂₄H₂₂ClF₂N₂O₄ requires 475.1231).

Example 727

3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-indol-5-yl]methyl}-6-methylpyridin-2(1H)-one

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with compound of Example 633 (200 mg, 0.48 mmol), 1-chlorocarbonyl-1-methylethyl acetate (104.3 μL, 0.72 mmol), triethylamine (133 μL, 0.96 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 20 min the reaction was completed by LC-MS. NaOH (2.5M, 2.24 mmol, 1.5 mL) and MeOH (2.0 mL) was added and stirred for 20 min to give the title compound. The compound precipitated out of solution. The precipitate was filtered and washed with water and diethyl ether to obtain a white solid (240 mg, 99%). ¹H NMR (400 MHz, (DMSO) δ 8.0 (d, J=8.3, 1H), 7.6 (q, J=8.6 and 6.9 Hz, 1H), 7.3 (td, J=2.5 and 7.8 Hz, 1H), 7.1 (td, J=1.75 and 6.7 Hz, 1H), 6.95 (s, 1H), 6.89 (d, J=8.5 Hz, 1H), 6.58 (s, 1H), 5.25 (s, 2H), 4.3 (t, J=8.3 Hz, 2H), 3.42 (t, J=5.4 Hz, 1H), 3.35 (t, J=5.2 Hz, 1H), 3.0 (t, J=8.2 Hz, 2H), 2.3 (s, 3H), 1.3 (s, 6H) ppm. ES-HRMS m/z 503.1561 (M+H calcd for C₂₆H₂₆ClF₂N₂O₄ requires 503.1544).

Example 728

3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(methoxyacetyl)-2,3-dihydro-1H-indol-5-yl]methyl}-6-methylpyridin-2(1H)-one

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with compound of Example 633 (200 mg, 0.48 mmol), methoxyacetyl chloride (66 μL, 0.72 mmol), triethylamine (134 μL, 0.96 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 20 min the reaction was completed by LC-MS. The compound precipitated out of solution. The precipitate was filtered and washed with water and diethyl ether to obtain a white solid (195 mg, 83%). ¹H NMR (400 MHz, (DMSO) δ 8.0 (d, J=8.0, 1H), 7.6 (q, J=8.6 and 6.7 Hz, 1H), 7.3 (td, J=2.4 and 6.7 Hz, 1H), 7.1 (td, J=1.88 and 6.6 Hz, 1H), 6.9 (s, 2H), 6.58 (s, 1H), 5.25 (s, 2H), 4.15 (s, 2H), 3.9 (t, J=8.3 Hz, 2H), 3.45 (m, 1H), 3.4 (m, 1H), 3.32 (s, 3H), 3.0 (t, J=8.5 Hz, 2H), 2.3 (s, 3H) ppm. ES-HRMS m/z 489.1387 (M+H calcd for C₂₅H₂₄ClF₂N₂O₄ requires 489.1387).

Example 729

5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylindoline-1-carboxamide

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with compound of Example 633 (200 mg, 0.48 mmol), dimethylcarbamyl chloride (66 μL, 0.72 mmol), triethylamine (133 μL, 0.96 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 5 min the reaction was completed by LC-MS. The compound precipitated out of solution. The precipitate was filtered and washed with water and diethyl ether to obtain a white solid (198 mg, 85%). ¹H NMR (400 MHz, (DMSO) δ 7.6 (q, J=7.4 Hz, 1H), 7.3 (t, J=8.9 Hz, 1H), 7.1 (t, J=8.5 Hz, 2H), 6.93 (s, 1H), 6.86 (s, 1H), 6.58 (s, 1H), 5.25 (s, 2H), 3.9 (t, J=8.2 Hz, 2H), 3.45 (m, 1H), 3.4 (m, 1H), 2.9 (t, J=8.3 Hz, 2H), 2.8 (s, 6H), 2.3 (s, 3H) ppm. ES-HRMS m/z 488.1548 (M+H calcd for C₂₅H₂₄ClF₂N₂O₄ requires 488.1547).

Example 730

3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(1-glycoloyl-2,3-dihydro-1H-indol-5-yl)methyl]pyridin-2(1H)-one

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with compound of Example 88 (200 mg, 0.5 mmol), acetoxyacetyl chloride (59 μL, 0.55 mmol), triethylamine (140 μL, 1.0 mmol) and tetrahydrofuran (3.0 mL). After stirring at 25° C. for 20 min the reaction was completed by LC-MS. NaOH (2.5M, 2.24 mmol, 1.0 mL) and MeOH (2.0 mL) was added and stirred for 20 min to give the title compound. The compound precipitated out of solution. The precipitated was filtered and washed with water and diethyl ether to obtain the title compound (200 mg, 83%) as a white solid. ¹H NMR (400 MHz, (DMSO) δ 7.98 (d, J=8.1, 1H), 7.9 (d, J=7.8 Hz, 1H), 7.6 (q, J=8.6 and 6.6 Hz, 1H), 7.3 (dt, J=2.4 and 7.2 Hz, 1H), 7.1 (m, 2H), 6.56 (d, J=7.8 Hz, 1H), 5.25 (s, 2H), 5.1 (s, 2H), 4.8 (t, J=5.8 Hz, 1H), 4.1 (d, J=5.6 Hz, 2H), 3.9 (t, J=7.9 Hz, 2H), 3.1 (t, J=7.9 Hz, 2H) ppm. ES-HRMS m/z 461.1088 (M+H calcd for C₂₃H₂₀ClF₂N₂O₄ requires 461.1074).

Example 731

Preparation of 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(1-glycoloyl-2,3-dihydro-1H-indol-5-yl)methyl]pyridin-2(1H)-one

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with compound of Example 88 (200 mg, 0.50 mmol), 1-chlorocarbonyl-1-methylethyl acetate (80 μL, 0.55 mmol), triethylamine (140 μL, 1.0 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 20 min the reaction was completed by LC-MS. NaOH (2.5M, 2.24 mmol, 1.5 mL) and MeOH (2.0 mL) was added and stirred for 20 min to give the title compound. The compound precipitated out of solution. The precipitated was filtered and washed with water and diethyl ether to obtain the title compound (136 mg, 55%) a white solid. ¹H NMR (400 MHz, (DMSO) δ 7.98 (d, J=8.1, 1H), 7.9 (d, J=7.8 Hz, 1H), 7.6 (q, J=8.6 and 6.6 Hz, 1H), 7.3 (m, 1H), 7.1 (m, 2H), 6.56 (d, J=7.8 Hz, 1H), 5.25 (s, 2H), 5.0 (s, 2H), 4.3 (t, J=7.8 Hz, 2H), 3.0 (t, J=7.9 Hz, 2H), 1.3 (s, 6H) ppm. ES-HRMS nz/z 489.1376 (M+H calcd for C₂₅H₂₄ClF₂N₂O₄ requires 489.1387).

Example 732

3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(methoxyacetyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound of Example 88 (200 mg, 0.5 mmol), methoxyacetyl chloride (69 μL, 0.75 mmol), triethylamine (139 μL, 1.0 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 20 min the reaction was completed by LC-MS. The compound precipitated out of solution. The precipitate was filtered and washed with water and diethyl ether to obtain a white solid (195 mg, 83%). ¹H NMR (400 MHz, (DMSO) δ 7.98 (d, J=8.2, 1H), 7.9 (d, J=7.7 Hz, 1H), 7.6 (d, J=8.5 Hz, 1H), 7.3 (t, J=9.6 Hz, 1H), 7.1 (m, 3H), 6.56 (d, J=7.8 Hz, 1H), 5.25 (s, 2H), 5.1 (s, 2H), 4.1 (s, 2H), 3.98 (t, J=7.9 Hz, 2H), 3.33 (s, 3H), 3.0 (t, J=7.9 Hz, 2H) ppm. ES-HRMS m/z 461.1088 (M+H calcd for C₂₃H₂₀ClF₂N₂O₄ requires 461.1074).

Example 733

5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylindoline-1-carboxamide

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound of Example 88 (200 mg, 0.5 mmol), dimethylcarbamyl chloride (69 μL, 0.75 mmol), triethylamine (139 μL, 1.0 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 5 min the reaction was completed by LC-MS. The compound precipitated out of solution. The precipitate was filtered and washed with water and diethyl ether to obtain a white solid (188 mg, 58%). ¹H NMR (400 MHz, (DMSO) δ 7.9 (d, J=8.1, 1H), 7.6 (q, J=8.6 and 6.6 Hz, 1H), 7.3 (t, J=9.3 Hz, 1H), 7.1 (m, 3H), 6.8 (d, J=8.0 Hz, 1H), 6.5 (d, J=7.8 Hz, H), 5.25 (s, 2H), 5.0 (s, 2H), 3.7 (t, J=8.6 Hz, 2H), 2.9(t, J=7.9 Hz, 2H), 2.8 (s, 6H) ppm. ES-HRMS m/z 474.1387 (M+H calcd for C₂₄H₂₃ClF₂N₃O₃ requires 474.1391).

Example 734

3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-hydroxy-6-methyl-pyridin-2(1H)-one

Ammonium hydroxide (concentrated, 500 mL) and 4-hydroxy-6-methylpyrone (500 g, (3.96 moles) were stirred at 85° C. in a 3 L flask filled with a short and wide air condenser with a trap to collect any overflow. Mechanical stirring was used to control extensive foaming during heating. After 2 h the product precipitated and the reaction mixture cooled and filtered. The filtrate was concentrated to provide additional product. The combined solids were dried (450 g). ¹H NMR (300 MHz, DMSO-d₆) δ 10.94 (br s, 1H), 10.34 (s, 1H), 5.59 (d, J=1.4 Hz, 1H), 5.32 (d, J=2.0 Hz, 1H), 2.07 (s, 3H).

Step 2: Preparation of 4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

4-Hydroxy-6-methyl-pyridin-2(1H)-one (375 g, 3 moles) was suspended in NMP (750 mL) and DBU (456 g, 3 moles) added in one portion. The mixture was heated to 60° C. with mechanical stirring. The 2,4-difluorobenzyl chloride (487.5 g, 3 moles) was added during a 20 min. period, and the mixture reached a final temperature of 80° C. After reaction for 3 h at this temperature, significant precipitation was observed. The mixture was cooled, with continuous stirring, first to ambient temperature then subsequently to 10° C., and then filtered. The precipitate was washed with cold CH₃CN (200 mL) followed by water (4×400 mL) and dried (373 g, 50%). MS (M+H) m/z 252.

Step 3: 3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

To a suspension of 4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (252 g, 1 mole) in AcOH (500 mL) at 25° C., bromine (160 g, 1 mole) was added drop-wise with stirring. At the end of the addition, 400 mL of water (400 mL) was added and stirring was continued for 30 min. The resulting white suspension was filtered and washed with water (400 mL, twice), saturated sodium bicarbonate (200 mL) and water (300 mL). The white solid was dried (326 g, 98%). ¹H NMR (300 MHz, DMSO-d₆) δ 11.98 (br s, 1H), 7.43 (app q, J=9 Hz, 1H), 7.23 (app t, J=10 Hz, 1H), 7.11 (app t, J=9 Hz, 1H), 6.28 (s, 1H), 5.20 (s, 2H), 2.25 (s, 3H). ES-HRMS nz/z 329.9973 (M+H calcd for C₁₃H₁₁BrF₂NO₂ requires 329.9947).

Example 735

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide

3-[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (see synthesis in Example 487, step 4) (1 g, 2.15 mmol) was dissolved in THF (20 ml), and 2-Chloro-4,6-dimethoxy-1,3,5-triazine (0.45 g, 2.58 mmol) and N-methyl morpholine (0.71 ml, 6.45 mmol) were added. The mixture was stirred at room temperature for 1 h. After that time, NH₄OH (5 ml) was added and the reaction stirred at room temperature for an additional hour. To the reaction mixture was added additional THF (50 ml) and water (200 ml). The mixture was extracted with ethyl acetate. The ethyl acetate extraction was washed with saturated brine solution. The brine layer was extracted with ethyl acetate. The organic layers were combined, dried over Na₂SO₄, filtered and the solvent was removed in vacuo. The residue was taken up in ethyl acetate and the resulting precipitate was collected on a filter pad to yield a white powder (0.71 g, 71%). ¹H NMR (300 MHz, CD₃OD) δ 7.97 (dd, J=6.04, 1.81 Hz, 1H), 7.70 (m, 2H), 7.57 (d, J=7.85 Hz, 1H), 7.13-7.06 (m, 2H), 6.71 (s, 1H), 5.40 (s, 2H), 2.13 (s, 3H) 2.04 (s, 3H). LC/MS, t_r=2.33 min. (5 to 95% acetonitrile/water over 5 min at 1 m/min with detection 254 nm, at 50° C.). ES-MS m/z 463 (M+H).

Example 736

(+)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide

The isolated product from Example 735 was separated using a Chiracel OJ column (50 mm×500 mm, 20 μm) eluting with 100% methanol, (50 ml/min), pressure 400 psi, with detection at 254 nm. Fractions of the early-eluting atropisomer were pooled and concentrated in vacuo to the title compound as a white solid (yield 99%), ee>98%. [□□_D=+16.30 (1.0 g/100 mL MeOH, 22° C.). ¹H NMR (300 MHz, CD₃OD), identical to product from Example 735. ES-HRMS m/z 463.0458 (M+H calcd for C₂₁H₁₈BrF₂N₂O₃ requires 463.0463).

Example 737

(−)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide

The title compound was prepared as with the title compound of Example 736, pooling fractions from the late-eluting atropisomer. Recovery by solvent concentration gave a white solid, (yield 90%), ee>98%. [□□_D=−15.9° (1.0 g/100 mL MeOH, 22° C.). ¹H NMR (300 MHz, CD₃OD), identical to product from Example 735. ES-HRMS m/z 463.0481 (M+H calcd for C₂₁H₁₈BrF₂N₂O₃ requires 463.0463).

Example 738

4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}-N-methylbenzamide

Step 1: Preparation of Methyl 4-(1-bromoethyl)benzoate

4-(1-Bromoethyl)benzoic acid (14.75 g, 64.4 mmol) was dissolved in 60 ml of methanol. 60 ml of 4 M HCl in 1,4-dioxane was added and stirred at room temperature over night. The solvent was evaporated to yield a tan oil (14.96 g, 96% yield). ¹H NMR (400 MHz, CDCl₃) δ 8.00-7.98 (m, 2H), 7.49-7.47 (m, 2H), 5.18 (q, J=6.89 Hz, 1H), 3.90 (s, 3H), 2.03 (d, J=6.85 Hz, 3H); LC/MS, t_r=2.77 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 243 (M+H).

Step 2: Preparation of Methyl 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoate

3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (Example 734) (8.0 g, 24.2 mmol) was stirred at room temperature with sodium hydride (60% dispersion in mineral oil) (1.94 g, 48.4 mmol) in 100 ml of tetrahydrofuran for 10 min. Methyl 4-(1-bromoethyl)benzoate (from step 1) (6.48 g, 26.6 mmol) and 60 ml of NMP were then added and refluxed at 105° C. over night. The tetrahydrofuran was evaporated and the reaction was then added into 1 L of water. No precipitate formed, and the solution was extracted three times with ethyl acetate. The combined organic layer was dried over MgSO₄ and evaporated. The resulting oil was triturated with diethyl ether and petroleum ether to obtain a solid which was filtered and dried in vacuo to give an off-white solid (7.35 g, 62%). ¹H NMR (400 MHz, CDCl₃) δ 7.98 (d, J=8.32 Hz, 2H), 7.55 (app q, J=8.46 Hz, 1H), 7.52 (d, J=8.32 Hz, 2H), 6.92 (dt, J=8.46, 2.02 Hz, 1H), 6.84 (dt, J=9.40, 2.06 Hz, 1H), 6.36 (s, 1H), 6.29 (q, J=6.58 Hz, 1H), 5.14 (s, 2H), 3.88 (s, 3H), 2.29 (s, 3H), 1.64 (d, J=6.57 Hz, 3H); LC/MS, t_r=3.93 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 514 (M+Na). ES-HRMS m/z 492.0629 (M+H calcd for C₂₃H₂₁BrF₂NO₄ requires 492.0617).

Step 3: Preparation of 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoic Acid

Methyl 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoate (from Step 2) (5.0 g, 10.15 mmol) was stirred with 8.2 ml of 2.5 N NaOH, 25 ml of tetrahydrofuran and 5 ml of water at room temperature for 48 h. The reaction was acidified with 1 N HCl and extracted twice with ethyl acetate. The combined organic layer was dried over MgSO₄ and evaporated. The resulting solid was dried in vacuo to yield a white solid (4.51 g, 93%). ¹H NMR (400 MHz, CDCl₃) δ 8.06 (d, J=8.46 Hz, 2H), 7.56 (d, J=8.33 Hz, 2H), 7.55 (app q, J=7.74 Hz, 1H), 6.92 (dt, J=8.33, 1.52 Hz, 1H), 6.84 (dt, J=9.47, 2.42 Hz, 1H), 6.37 (s, 1H), 6.31 (q, J=6.53 Hz, 1H), 5.14 (s, 2H), 2.30 (s, 3H), 1.65 (d, J=6.58 Hz, 3H); LC/MS, t_r=3.25 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 500 (M+Na). ES-HR/MS m/z 476.0311 (M−H calcd for C₂₂H₁₇BrF₂NO₄ requires 476.0309).

Step 4: Preparation of the title compound. 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoic acid (from Step 3) (500 mg, 1.04 mmol) was dissolved in 5 ml of methylene chloride. 2.0 M methylamine in tetrahydrofuran (2.09 ml, 4.18 mmol) was added, followed, in order, by EDCI (250 mg, 1.31 mmol), 1-hydroxybenzotriazole (177 mg, 1.31 mmol) and triethylamine (290 μl, 2.08 mmol). The reaction was stirred at room temperature overnight. The reaction was quenched with saturated ammonium chloride solution and extracted twice with ethyl acetate. The combined organic layer was washed with saturated NaHCO₃ solution and water, dried over MgSO₄ and evaporated. Water was used to triturate the product. The resulting solid was filtered, washed with water, and dried in vacuo to give a white solid (355 mg, 69%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.34 (app d, J=3.75 Hz, 1H), 7.75 (d, J=7.92 Hz, 2H), 7.62 (app q, J=7.74 Hz, 1H), 7.46 (d, J=7.92 Hz, 2H), 7.30 (app t, J=9.20 Hz, 1H), 7.14 (app t, J=7.72 Hz, 1H), 6.83 (s, 1H), 6.23 (q, J=6.44 Hz, 1H), 5.21 (s, 2H), 2.73 (d, J=3.83 Hz, 3H), 2.28 (s, 3H), 1.54 (d, J=6.31 Hz, 3H); LC/MS, t_r=3.02 min. (5 to 95% acetonitrile/water over 5 min. at 1 m/min, at 254 nm, at 50° C.), ES-MS m/z 513 (M+Na). ES-HRMS m/z 491.0738 (M+H calcd for C₂₃H₂₂BrF₂N₂O₃ requires 491.0776).

Example 739

4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzamide

4-{1-[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoic acid (from Example 738, step 3) (500 mg, 1.04 mmol) was dissolved in 5 ml of methylene chloride. 0.5 M ammonia in 1,4-dioxane (20.8 ml, 10.4 mmol) was added, followed, in order, by EDCI (250 mg, 1.31 mmol), 1-hydroxybenzotriazole (177 mg, 1.31 mmol) and triethylamine (290 μl, 2.08 mmol). The reaction was stirred at room temperature overnight. The reaction was evaporated and the resulting oil was dissolved in acetonitrile. An impurity precipitated out and was filtered off. The filtrate was evaporated and re-dissolved in diethyl ether/ethyl acetate. A precipitate formed. The resulting solid was filtered and dried in vacuo to give a white solid (300 mg, 60%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.88 (br s, 1H), 7.80 (d, J=8.19 Hz, 2H), 7.62 (app q, J=7.92 Hz, 1H), 7.46 (d, J=8.19 Hz, 2H), 7.16-7.13 (m, 2H), 7.14 (dt, J=8.46, 2.01 Hz, 1H), 6.84 (s, 1H), 6.23 (q, J=6.44 Hz, 1H), 5.22 (s, 2H), 2.28 (s, 3H), 1.54 (d, J=6.45 Hz, 3H); LC/MS, t_r=2.90 min. (5 to 95% acetonitrile/water over 5 min. at 1 m/min, at 254 nm, at 50° C.), ES-MS m/z 499 (M+Na). ES-HRMS m/z 477.0626 (M+H calcd for C₂₂H₂₀BrF₂N₂O₃ requires 477.0620).

Example 740

3-Bromo-4-[(2,4-difluorobenzyl)oxy]-1-{1-[4-(hydroxymethyl)phenyl]ethyl}-6-methylpyridin-2(1H)-one

4-{1-[3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoic acid (from Example 738, step 3) (500 mg, 1.04 mmol) was added to a solution of 1M borane-dimethylsulfide complex in tetrahydrofuran (1.56 ml, 3.12 mmol) in 2.5 ml tetrahydrofuran at 0° C. The reaction was allowed to warm to room temperature while stirring. After stirring 48 h, ice chips were added to quench the reaction. The reaction was extracted twice with ethyl acetate and the combined organic layers were washed with brine, dried over MgSO₄ and evaporated. The resulting oil did not solidify, so it was dried in vacuo to give a clear oil (320 mg, 66%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.62 (app q, J=7.92 Hz, 1H), 7.35 (d, J=8.05 Hz, 2H), 7.30 (dt, J=9.93, 2.46 Hz, 1H), 7.24 (d, J=7.92 Hz, 2H), 7.14 (dt, J=8.53, 2.46 Hz, 1H), 6.82 (s, 1H), 6.19 (q, J=6.49 Hz, 1H), 5.21 (s, 2H), 5.09 (t, J=5.71 Hz, 1H), 4.42 (d, J=5.64 Hz, 2H), 2.29 (s, 3H), 1.52 (d, J=6.44 Hz, 3H); LC/MS, t_r=3.14 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 486 (M+Na). ES-HRMS m/z 464.0658 (M+H calcd for C₂₂H₂₁BrF₂NO₃ requires 464.0667).

Example 741

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]methyl}benzoic Acid

Step 1: Preparation of Methyl {[4-hydroxy-6-(acetoxymethyl)-2-oxopyridin-1(2H)-yl]methyl}benzoate

Methyl-4-(aminomethyl)benzoate (15.5 g, 94 mmol) and 3-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-2-oxopropyl acetate (see synthesis in Example 653, Step 1) (24.9 g, 103 mmol) were dissolved in 1,4 dioxane. The reaction was heated to reflux for 3 h with stirring. The reaction was cooled to room temperature and methanesulfonic acid (6.1 mL, 94 mmol) was added. The resulting mixture was heated to reflux and stirred for 15 min. The reaction was cooled to room temperature acidified with 0.5 N HCl and extracted with ethyl acetate (3×300 mL). The organic extracts were combined washed with brine, dried over Na₂SO₄ and filtered. The filtrate was concentrated to an oil that was triturated in a mixture of CH₂Cl₂ and EtOAc to yield a white solid that was collected and dried (8.5 g, 27%). ¹H NMR (400 MHz, CDCl₃) δ 7.96 (d, J=8.0 Hz, 2H), 7.17 (d, J=8.0 Hz, 2H), 6.20 (app d, J=2.4 Hz, 1H), 5.90 (app d, J=2.4 Hz, 1H), 5.33 (br s, 2H), 4.95 (s, 2H); 3.87 (s, 3H); 1.80 (s, 3H). ES-MS m/z 316 (M+H). LC/MS, t_r=1.81 min (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 332 (M+H). ES-HRMS m/z 332.1160 (M+H calcd for C₁₇H₁₈NO₆ requires 332.1129).

Step 2: Preparation of Methyl{[3-bromo-4-hydroxy-6-(acetoxymethyl)-2-oxopyridin-1(2H)-yl]methyl}benzoate

Methyl{[4-hydroxy-6-(acetoxymethyl)-2-oxopyridin-1(2H)-yl]methyl}benzoate (from Step 1) (8.3 g, 25.2 mmol) was suspended in acetonitrile and N-bromosuccinimide (4.9 g, 27.7 mmol) was added. The reaction was stirred at room temperature for 30 min. after which the reaction was concentrated on a rotary evaporator and the resulting solid was washed with acetonitrile and dried in vacuo to yield a white solid (10.7 g, 104%). ¹H NMR (400 MHz, CDCl₃) δ 7.97 (d, J=8.4 Hz, 2H), 7.17 (d, J=8.4 Hz, 2H), 6.26 (s, 1H), 5.38 (br s, 2H), 4.85 (s, 2H); 3.88 (s, 3H); 1.94 (s, 3H). LC/MS, t_r=1.86 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 410.3 (M+H).

Step 3: Preparation of Methyl{[3-bromo-4-(2,4-difluorobenzyl)oxy]-6-(acetoxymethyl)-2-oxopyridin-1(2H)-yl]methyl}benzoate

Methyl{[3-bromo-4-hydroxy-6-(acetoxymethyl)-2-oxopyridin-1(2H)-yl]methyl}benzoate (from Step 2) (10.7 g, 26 mmol) was suspended in N,N-dimethylformamide and 2,4-difluorobenzyl bromide (5.1 mL, 28.6 mmol) and K₂CO₃ (4 g, 28.6 mmol) were added. The reaction was stirred at room temperature for 1 h. after which the reaction was partitioned between water and ethyl acetate and extracted with ethyl acetate (4×150 mL). The organic extracts were combined washed with brine, dried over Na₂SO₄, filtered and concentrated to an oil that deposited a tan solid on standing. This resulting solid was washed with ether and dried (7.9 g, 57%). ¹H NMR (400 MHz, CDCl₃) δ 7.96 (d, J=8.4 Hz, 2H), 7.55 (app q, J=7.6 Hz, 1H), 7.18 (d, J=8.4 Hz, 2H), 6.94 (app dt, J=2.0, 8.4 Hz, 1H), 6.88-6.83 (m, 1H), 6.27 (s, 1H), 5.41 (br s, 2H); 5.24 (s, 2H) 4.88 (s, 2H), 3.88 (s, 3H); 1.96 (s, 3H). ES-HRMS m/z 536.0510 (M+H calcd for C₂₄H₂₁F₂BrNO₆ requires 536.0515).

Step 4: Preparation of the title compound. Methyl{[3-bromo-4-(2,4-difluorobenzyl)oxy]-6-(acetoxymethyl)-2-oxopyridin-1(2H)-yl]methyl}benzoate (from Step 3) (2 g, 3.7 mmol) was suspended in a mixture of methanol: tetrahydrofuran (1:4). Aqueous sodium hydroxide (4 N, 4 mL, 16 mmol) was added and the reaction was stirred at room temperature for 6 h. 1 N Hydrochloric acid was added affording a white precipitate that was collected, washed with water, and dried (1.7 g, 94%). ¹H NMR (400 MHz, CD₃OD) δ 7.97 (d, J=8.0 Hz, 2H), 7.62 (app q, J=7.6 Hz, 1H), 7.19 (d, J=8.0 Hz, 2H), 7.05-7.00 (m, 2H), 6.72 (s, 1H), 5.48 (br s, 2H); 5.34 (s, 2H) 4.46 (s, 2H). ES-HRMS m/z 480.0296 (M+H calcd for C₂₁H₁₇F₂BrNO₅ requires 480.0253).

Example 742

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]methyl}-N-methylbenzamide

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]methyl}benzoic acid (from Example 741, Step 4) (1.4 g, 2.9 mmol) was dissolved in N,N-dimethylacetamide, and 1-hydroxybenzotriazole (1 M in N,N-dimethylacetamide, 2.9 mL, 2.9 mmol) was added, followed by methylamine (2M in tetrahydrofuran, 1.75 mL), 4-methylmorpholine (1 mL, 8.7 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (556 mg, 2.9 mmol). The reaction was stirred at room temperature overnight. The reaction mixture was then partitioned between water and ethyl acetate and extracted with ethyl acetate (4×150 mL). The organic extracts were combined, washed with saturated sodium bicarbonate, brine, and dried over Na₂SO₄. The extract was filtered and concentrated to an oil that was triturated with a mixture of methylene chloride, ether, and ethyl acetate to give a tan solid that was dried in vacuo (1.1 g, 80%). ¹H NMR (400 MHz, d7 DMF) δ 8.43 (app d, J=4.0 Hz, 1H), 7.89 (d, J=8.0 Hz, 2H), 7.73 (app q, J=7.6 Hz, 1H), 7.26 (d, J=8.4 Hz, 2H), 7.33-7.18 (m, 2H), 6.78 (s, 1H), 6.13 (br s, 1H); 5.47 (br s, 2H); 5.41 (s, 2H) 4.54 (s, 2H), 2.84 (d, J=4.8 Hz, 3H). ES-HRMS m/z 493.0574 (M+H calcd for C₂₂H₂₀F₂BrN₂O₄ requires 493.0569).

Example 743

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-{4-[(methylamino)methyl]benzyl}pyridin-2(1H)-one

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]methyl}-N-methylbenzamide (0.5 g, 1.0 mmol) was dissolved in 1,4 dioxane, and borane-methyl sulfide complex (2 M in tetrahydrofuran, 1.5 mL) was added and the reaction was heated to 65° C. with stirring for 6 h. Additional borane-methyl sulfide complex (2 mL) was added and the reaction was stirred for 70 h. at 65° C. The reaction was quenched with 1N aqueous hydrochloric acid, and the reaction was concentrated in vacuo at 50° C. yielding an oil that was partitioned between water and ether. The ether extract was removed and the aqueous layer was adjusted to pH=11 with 2.5 N sodium hydroxide. The aqueous was extracted with ethyl acetate (3×100 mL) and the organic extracts were combined washed with brine, dried over Na₂SO₄, filtered and concentrated to oil that was triturated with ether to give a tan solid that was dried in vacuo (68 mg, 14%). ¹H NMR (400 MHz, CD₃OD) δ 7.61 (app q, J=7.6 Hz, 1H), 7.37 (d, J=8.0 Hz, 2H), 7.17 (d, J=8.4 Hz, 2H), 7.05-7.01 (m, 2H), 6.71 (s, 1H), 5.43 (br s, 2H); 5.34 (s, 2H), 4.47 (s, 2H), 3.98 (s, 2H), 2.57 (s, 3H). ES-HRMS m/z 479.0806 (M+H calcd for C₂₂H₂₂F₂BrN₂O₃ requires 479.0776).

Exmaple 744

1-{[5-(aminomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 1-{[5-(Chloromethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

Cyanuric chloride (5.1 g, 27.6 mmol) was dissolved in N,N-dimethylformamide and stirred for 1 hour, after which 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)pyrazin-2-yl]methyl}-6-methylpyridin-2(1H)-one (12 g, 26.5 mmol) was added. The reaction was stirred at room temperature for 2 h. and was then partitioned between water and ethyl acetate then extracted with ethyl acetate (3×200 mL). The organic extracts were combined, washed with 2M Na₂CO₃ (1×200 mL), 0.5 N HCl (1×200 mL), and brine, then dried over Na₂SO₄, and filtered. The filtrate was concentrated in vacuo yielding an oil that was triturated with ether affording an orange solid that was dried (10.4 g, 84%). ¹H NMR (400 MHz, CDCl₃) δ 8.69 (s, 1H), 8.58 (s, 1H), 7.53 (app q, J=8.0 Hz, 1H), 6.92 (app t, J=8.0 Hz, 1H), 6.87-6.80 (m, 1H), 6.03 (s, 1H), 5.36 (br s, 2H), 5.19 (s, 2H); 3.45 (s, 2H); 2.52 (s, 3H). ES-MS m/z 470 (M+H). LC/MS, t_r=2.66 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.).

Step 2: Preparation of 1-{[5-(phthalimidomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

1-{[5-(Chloromethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (from Step 1) (10.4 g, 22.1 mmol) was suspended in tetrahydrofuran and a solution of potassium phthalimide (4.9 g, 26.5 mmol) in N,N-dimethylformamide was added. The reaction was stirred at room temperature for 20 h., after which the reaction mixture was concentrated in vacuo. Addition of water to the resulting oil afforded a precipitate that was collected and dried, yielding a white solid (7.3 g, 57%). ¹H NMR (400 MHz, CDCl₃) δ 8.61 (app d, J=1.6 Hz, 1H), 8.49 (app d, J=1.2 Hz, 1H), 7.87-7.84 (m, 2H), 7.75-7.71 (m, 2H), 7.53 (app q, J=7.6 Hz, 1H), 6.92 (app dt, J=1.6, 8.4 Hz, 1H), 6.90-6.80 (m, 1H), 5.99 (s, 1H), 5.33 (br s, 2H), 5.18 (s, 2H); 4.99 (s, 2H); 2.49 (s, 3H). ES-MS nz/z 581 (M+H). LC/MS, t_r=2.85 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.).

Step 3: Preparation of the title compound. 1-{[5-(phthalimidomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (from Step 2) (7.3 g, 12.5 mmol) was dissolved in 1,4 dioxane and hydrazine monohydrate (0.75 mL, 15 mmol) was added. The reaction was heated to 85° C. with stirring for 22 h. The reaction mixture was concentrated in vacuo yielding a white paste that was treated with 1N aqueous hydrochloric acid to afford a white precipitate that was collected and then stirred in 1N sodium hydroxide for 1 h. The resulting solid was filtered and dried (5.5 g, 98%). ¹H NMR (400 MHz, CDCl₃) δ 8.67 (s, 1H), 8.43 (s, 1H), 7.54 (app q, J=8.0 Hz, 1H), 6.93 (app dt, J=1.6, 8.4 Hz, 1H), 6.87-6.81 (m, 1H), 6.02 (s, 1H), 5.35 (br s, 2H), 5.19 (s, 2H); 3.96 (s, 2H); 2.53 (s, 3H). ES-HRMS m/z 451.0593 (M+H calcd for C₁₉H₁₈BrF₂N₄O₂ requires 451.0576).

Example 745

2-{[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]amino}-2-oxoethyl Acetate

Acetoxyacetic acid (520 mg, 4.4 mmol) was dissolved in N,N-dimethylacetamide, and 1-hydroxybenzotriazole (1M in N,N-dimethylacetamide, 4.4 mL) and 4-methylmorpholine (0.725 mL, 6.6 mmol) were added. 1-{[5-(aminomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (1 g, 2.2 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (840 mg, 4.4 mmol) were added and the reaction stirred at room temperature. After 1 h. the reaction mixture was partitioned between water and ethyl acetate and extracted with ethyl acetate (4×150 mL). The organic extracts were combined, washed with saturated aqueous sodium bicarbonate, brine, and dried over Na₂SO₄. The extract was filtered and concentrated to an oil that was triturated with ether to give a solid that was dried in vacuo. The resulting solid was purified by chromatography (silica gel, hexane/ethyl acetate) to yield an off-white solid (350 mg, 30%). ¹H NMR (400 MHz, CDCl₃) δ 8.74 (s, 1H); 8.50 (s, 1H); 7.53 (app q, J=8.0 Hz, 1H), 7.18 (br s, 1H), 6.93 (app t, J=8.4 Hz, 1H), 6.87-6.82 (m, 1H); 6.04 (s, 1H), 5.35 (s, 2H), 5.20 (s, 2H); 4.61 (s, 2H); 4.60 (s, 2H); 2.57 (s, 3H); 2.19 (s, 3H). ES-HRMS m/z 551.0721 (C₂₃H₂₂BrF₂N₄O₅ requires 551.0736).

Example 746

N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-hydroxyacetamide

2-{[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]amino}-2-oxoethyl acetate (255 mg, 0.46 mmol) was suspended in methanol/water (5:1) and K₂CO₃ (35 mg, 0.25 mmol) was added. The reaction was stirred at room temperature for 30 min. The reaction was then concentrated to and oil that was triturated with water to yield a white solid that was filtered and dried (175 mg, 75%). ¹H NMR (400 MHz, CD₃OD) δ 8.58 (s, 1H); 8.47 (s, 1H); 7.60 (app q, J=8.0 Hz, 1H), 7.14-6.98 (m, 2H); 6.50 (s, 1H), 5.45 (s, 2H), 5.29 (s, 2H); 4.61 (s, 2H); 4.01 (s, 2H); 2.54 (s, 3H). ES-HRMS m/z 509.0628 (C₂₁H₂₀BrF₂N₄O₄ requires 509.0630).

Example 747

N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]acetamide

1-{[5-(aminomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (500 mg, 1.1 mmol) was dissolved in N,N-dimethylformamide (5 mL). N,N-Diisopropylethylamine (0.75 mL, 4.4 mmol) was added followed by acetic anhydride (0.3 mL, 3.2 mmol). The reaction was stirred at room temperature for 2 h. and concentrated in vacuo to an oil, that was triturated in ether to yield an off-white solid that was collected and dried (252 mg, 46%). ¹H NMR (400 MHz, CDCl₃) δ 8.69 (s, 1H); 8.44 (s, 1H); 7.54 (app q, J=8.0 Hz, 1H), 6.93 (app t, J=8.4 Hz, 1H), 6.85 (app t, J=8.4 Hz, 1H), 6.03 (s, 1H), 5.33 (s, 2H), 5.19 (s, 2H); 4.53 (d, J=5.2 Hz, 2H); 2.52 (s, 3H); 2.03 (s, 3H). ES-HRMS m/z 493.0692 (C₂₁H₂₀BrF₂N₄O₃ requires 493.0681).

Example 748

N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]methanesulfonamide

1-{[5-(aminomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (500 mg, 1.1 mmol) was dissolved in N,N-dimethylformamide (5 mL). 4-Methylmorpholine (0.48 mL, 4.4 mmol) was added followed by methanesulfonyl chloride (0.17 mL, 2.2 mmol). The reaction was stirred at room temperature for 2 h. The reaction was then diluted with tetrahydrofuran (40 mL) and polyamine resin (1 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (2 g, 1.38 mmol/g) were added. The mixture was shaken for 20 h., filtered, and the resulting filtrate concentrated to an oil that was purified by chromatography (silica gel, hexane/ethyl acetate) to yield an off-white solid (133 mg, 23%). ¹H NMR (400 MHz, CDCl₃) δ 8.70 (s, 1H); 8.48 (s, 1H); 7.54 (app q, J=8.0 Hz, 1H), 6.93 (app t, J=8.4 Hz, 1H), 6.86-6.82 (m, 1H), 6.04 (s, 1H), 5.35 (s, 2H), 5.19 (s, 2H); 4.46 (s, 2H); 2.96 (s, 3H); 2.54 (s, 3H). ES-HRMS m/z 529.0354 (C₂₀H₂₀BrF₂N₄O₄S requires 529.0351).

Example 749

Methyl (5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methylcarbamate

1-{[5-(aminomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (500 mg, 1.1 mmol) was dissolved in N,N-dimethylformamide (5 mL). N,N-Diisopropylethylamine (0.75 mL, 4.4 mmol) was added, followed by methyl chloroformate (0.1 mL, 1.37 mmol) and the reaction was stirred at room temperature for 15 min. The reaction was then diluted with tetrahydrofuran (40 mL) and polyamine resin (1 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (2 g, 1.38 mmol/g) were added. The mixture was shaken for 20 h., filtered, and the resulting filtrate concentrated to an oil that was purified by chromatography (silica gel, hexane/ethyl acetate) to yield an off-white solid (137 mg, 24%). ¹H NMR (400 MHz, CDCl₃) δ 8.69 (s, 1H); 8.46 (s, 1H); 7.54 (app q, J=8.0 Hz, 1H), 6.93 (app t, J=8.4 Hz, 1H), 6.87-6.82 (m, 1H), 6.02 (s, 1H), 5.35 (s, 2H), 5.20 (s, 2H); 4.48 (d, J=5.2 Hz, 2H); 3.68 (s, 3H); 2.54 (s, 3H). ES-HRMS m/z 509.0619 (C₂₁H₂₀BrF₂N₄O₄ requires 509.0630).

Example 750

N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-hydroxy-2-methylpropanamide

2-Hydroxyisobutyric acid (230 mg, 2.2 mmol) was dissolved in N,N-dimethylformamide, and 1-hydroxybenzotriazole (1M in N,N-dimethylacetamide, 2.2 mL) and 4-methylmorpholine (0.36 mL, 3.3 mmol) were added. 1-{[5-(aminomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.5 g, 1.1 mmol) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (425 mg, 2.2 mmol) were then added. The reaction was stirred at room temperature. After 3 h., the reaction mixture was partitioned between water and ethyl acetate and extracted with ethyl acetate (4×150 mL). The organic extracts were combined, washed with saturated aqueous sodium bicarbonate, brine, and dried over Na₂SO₄. The extract was filtered and concentrated to an oil that was triturated with ether to give a solid that was dried in vacuo (275 mg, 46%). ¹H NMR (400 MHz, CDCl₃) δ 8.68 (s, 1H); 8.44 (s, 1H); 7.60-7.53 (m, 2H), 6.93 (app t, J=8.4 Hz, 1H), 6.87-6.82 (m, 1H); 6.03 (s, 1H), 5.34 (s, 2H), 5.19 (s, 2H); 4.55 (d, J=5.6 Hz, 2H); 2.54 (s, 3H); 1.45 (s, 6H). ES-HRMS m/z 537.0988 (C₂₃H₂₄BrF₂N₄O₄ requires 537.0943).

Example 751

N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-1-hydroxycyclopropanecarboxamide

By following the general method of Example 750 and substituting 1-hydroxy-1-cyclopropanecarboxylic acid (225 mg, 2.2 mmol) for 2-hydroxyisobutyric acid, the title compound was prepared and purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an off-white solid (90 mg, 15%). ¹H NMR (400 MHz, CDCl₃) δ 8.68 (s, 1H); 8.47 (s, 1H); 7.40 (app q, J=8.4 Hz, 1H), 6.93 (app t, J=8.4 Hz, 1H), 6.87-6.82 (m, 1H); 6.04 (s, 1H), 5.34 (s, 2H), 5.20 (s, 2H); 4.59 (d, J=5.6 Hz, 2H); 2.55 (s, 3H); 1.32(q, J=4.4 Hz, 2H), 1.04 (q, J=4.4 Hz, 2H). ES-HRMS m/z 535.0779 (C₂₃H₂₂BrF₂N₄O₄ requires 535.0787).

Example 752

N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]glycinamide Hydrochloride

By following the general method of Example 750 and substituting Boc-glycine (385 mg, 2.2 mmol) for 2-hydroxyisobutyric acid and allowing the reaction to proceed for 20 h., the title compound was prepared as its Boc-protected intermediate which was purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an off-white solid. Deprotection was accomplished with 4N HCl in 1,4 dioxane to afford the title compound as its hydrochloride salt (105 mg, 18%). ¹H NMR (400 MHz, CD₃OD) δ 8.60 (s, 1H); 8.50 (s, 1H); 7.60 (app q, J=8.4 Hz, 1H), 7.06-6.94 (m, 2H); 6.52 (s, 1H), 5.44 (s, 2H), 5.29 (s, 2H); 4.56 (s, 2H); 3.72 (s, 2H); 2.54 (s, 3H). ES-HRMS m/z 508.0799 (C₂₁H₂₁BrF₂N₅O₃ requires 508.0790).

Example 753

N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-L-alanineamide Hydrochloride

Polymer-bound carbodiimide resin (3.4 g, 1.18 meq/g, 4 mmol) was suspended in N,N-dimethylacetamide. Boc-L-Alanine (378 mg, 2 mmol) was added, followed by 1-hydroxybenzotriazole (1M in N,N-dimethylacetamide, 0.25 mL), 1-{[5-(aminomethyl)pyrazin-2-yl)methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.45 g, 1 mmol) and N,N-diisopropylethylamine (0.52 mL, 3 mmol). The reaction was shaken for 4 h. and then diluted with tetrahydrofuran. Polyamine resin (1 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (2 g, 1.38 mmol/g) were added and the mixture was shaken for 72 h., filtered and the resulting filtrate concentrated in vacuo. The crude product was purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an off-white solid. Deprotection was accomplished with 4N HCl in 1,4 dioxane to afford the title compound as its hydrochloride salt (116 mg, 22%). ¹H NMR (400 MHz, CD₃OD) δ 8.61 (s, 1H); 8.50 (s, 1H); 7.61 (app q, J=8.4 Hz, 1H), 7.05-6.99 (m, 2H); 6.53 (s, 1H), 5.45 (s, 2H), 5.29 (s, 2H); 4.55 (d, J=4.4 Hz, 2H); 3.98 (q, J=8.0 Hz, 1H); 2.55 (s, 3H); 1.50 (d, J=7.2 Hz, 3H). ES-MS m/z 522 (M+H). LC/MS, t_r=1.92 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.).

Example 754

N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-N-methylglycineamide Hydrochloride

By following the general method of Example 753 and substituting Boc-sarcosine (378 mg, 2 mmol) for Boc-L-alanine the title compound was prepared as its Boc-protected intermediate that was purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an off-white solid. Deprotection was accomplished with 4N HCl in 1,4 dioxane to afford the title compound as its hydrochloride salt (155 mg, 30%). ¹H NMR (400 MHz, CD₃OD) δ 8.61 (s, 1H); 8.52 (s, 1H); 7.60 (app q, J=8.4 Hz, 1H), 7.05-6.99 (m, 2H); 6.53 (s, 1H), 5.45 (s, 2H), 5.29 (s, 2H); 4.56 (s, 2H); 3.85 (s, 2H), 2.71 (s, 3H), 2.55 (s, 3H). ES-MS m/z 522 (M+H). LC/MS, t_r=1.86 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.).

Example 755

N¹-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-L-serineamide Hydrochloride

By following the general method of Example 753 and substituting Boc-serine (410 mg, 2 mmol) for Boc-L-alanine the title compound was prepared as its Boc-protected intermediate that was purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an off-white solid. Deprotection was accomplished with 4N HCl in 1,4 dioxane to afford the title compound as its hydrochloride salt (95 mg, 17%). ¹H NMR (400 MHz, CD₃OD) δ 8.60 (s, 1H); 8.51 (s, 1H); 7.61 (app q, J=8.4 Hz, 1H), 7.05-6.99 (m, 2H); 6.53 (s, 1H), 5.45 (s, 2H), 5.29 (s, 2H), 4.57 (s, 2H), 4.05-3.85 (m, 3H), 2.55 (s, 3H). ES-MS m/z 538 (M+H). LC/MS, t_r=1.92 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.)

Example 756

N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)alaninamide Hydrochloride

Polymer-bound carbodiimide resin (2.3 g, 1.18 meq/g, 2.7 mmol) was suspended in N,N-dimethylacetamide. Boc-L-Alanine (251 mg, 1.33 mmol) was added, followed by 1-hydroxybenzotriazole (1M in N,N-dimethylacetamide, 0.16 mL), 1-[4-(aminomethyl)benzyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.3 g, 0.67 mmol) and N,N-diisopropylethylamine (0.35 mL, 2 mmol). The reaction was shaken for 4 h. and then diluted with tetrahydrofuran. Polyamine resin (1 g, 2.81 mmol/g) and methylisocyanate functionalized polystyrene (2 g, 1.38 mmol/g) were added and the mixture was shaken for 22 h., filtered and the resulting filtrate concentrated in vacuo to an oil that was triturated in ether yielding an off-white solid. The solid was purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding the Boc-protected intermediate as an off-white solid. Deprotection was accomplished with 4N HCl in 1,4 dioxane to afford the title compound as its hydrochloride salt (134 mg, 36%). ¹H NMR (400 MHz, CD₃OD) δ 7.59 (app q, J=8.4 Hz, 1H), 7.50 (d, J=7.2 Hz, 2H); 7.08 (d, J=7.2 Hz, 2H); 7.00 (app t, J=8.4 Hz, 2H); 6.48 (s, 1H), 5.38 (s, 2H), 5.27 (s, 2H); 4.36 (s, 2H), 3.89 (app d, J=5.6 Hz, 1H); 2.34 (s, 3H); 1.47 (d, J=6.0 Hz, 3H). ES-MS m/z 520 (M+H). LC/MS, t_r=2.15 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.).

Example 757

N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N-methylglycinamide Hydrochloride

By following the general method of Example 756 and substituting Boc-sarcosine (251 mg, 1.33 mmol) for Boc-L-alanine the title compound was prepared as its Boc-protected intermediate that was purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an off-white solid. Deprotection was accomplished with 4N HCl in 1,4 dioxane to afford the title compound as its hydrochloride salt (160 mg, 39%). ¹H NMR (400 MHz, CD₃OD) δ 7.61 (q, J=8.4 Hz, 1H), 7.27 (d, J=8.0 Hz, 2H); 7.96 (d, J=8.0 Hz, 2H); 7.05-7.00 (m, 2H); 6.50 (s, 1H), 5.40 (s, 2H), 5.29 (s, 2H); 4.39 (s, 2H), 3.79 (s, 2H), 2.70 (s, 3H); 2.35 (s, 3H). ES-MS m/z 520 (M+H). LC/MS, t_r=2.15 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.).

Example 758

N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)serinamide Hydrochloride

By following the general method of Example 756 and substituting Boc-serine (273 mg, 1.33 mmol) for Boc-L-alanine the title compound was prepared as its Boc-protected intermediate that was purified by chromatography (silica gel, hexane/ethyl acetate/methanol) yielding an off-white solid. Deprotection was accomplished with 4N HCl in 1,4 dioxane to afford the title compound as its hydrochloride salt (95 mg, 25%). ¹H NMR (400 MHz, CD₃OD) δ 7.60 (q, J=8.4 Hz, 1H), 7.27 (d, J=8.0 Hz, 2H); 7.08 (d, J=8.0 Hz, 2H); 7.03-6.98 (m, 2H); 6.49 (s, 1H), 5.39 (br s, 2H), 5.28 (s, 2H); 4.39 (app d, J=2.4 Hz, 2H), 3.93 (s, 2H), 3.92-3.82 (m, 1H); 2.35 (s, 3H). ES-MS m/z 536 (M+H). LC/MS, t_r=2.14 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.).

Example 759

N¹-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)prolineamide Hydrochloride

By following the general method of Example 756 and substituting Boc-proline (286 mg, 1.33 mmol) for Boc-L-alanine the title compound was prepared as its Boc-protected intermediate that was triturated in ether yielding an off-white solid. Deprotection was accomplished with 4N HCl in 1,4 dioxane to afford the title compound as its hydrochloride salt (220 mg, 56%). ¹H NMR (400 MHz, CD₃OD) δ 7.60 (q, J=8.4 Hz, 1H), 7.25 (d, J=7.6 Hz, 2H); 7.08 (d, J=7.6 Hz, 2H); 7.03-6.98 (m, 2H); 6.50 (s, 1H), 5.38 (br s, 2H), 5.27 (s, 2H); 4.38 (s, 2H), 4.29-4.26 (m, 1H), 3.70-3.32 (m, 2H); 2.34 (s, 3H), 2.04-1.97 (m, 4H). ES-MS m/z 546 (M+H). LC/MS, t_r=2.18 min. (5 to 95% acetonitrile/water over 6 min. at 1 ml/min with detection 254 nm, at 50° C.).

Example 760

4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzenesulfonamide

Step 1. Preparation of 4-[(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)methyl]benzenesulfonamide

p-Aminomethyl benzene sulfonamide hydrochloride (17.66 g, 79.3 mmol) was suspended in H₂O (100 mL) and then 2.5 N NaOH was added to adjust the solution to pH 8. 4-Hydroxy-6-methyl-2-pyrone (10.0 g, 79.3 mmol) was added and the resulting mixture was heated at reflux for 22 h. The reaction mixture was cooled in an ice-bath and the precipitate that developed was collected by filtration washing with acetonitrile and then diethyl ether to give a tan solid (5.27 g, 23%). ¹H NMR (400 MHz, DMSO-d₆) δ 10.56 (s, 1H), 7.44 (d, J=8.3 Hz, 2H), 7.22 (d, J=8.3 Hz, 2H), 5.81 (d, J=2.0 Hz, 1H), 5.58 (d, J=2.6 Hz, 1H), 5.22 (s, 2H), 2.13 (s, 3H).

Step 2. Preparation of 4-{[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzenesulfonamide

4-[(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)methyl]benzenesulfonamide (Step 1) (1.00 g, 3.40 mmol) was suspended in dichloromethane (30 mL) and cooled in an ice-bath. To the suspension was added 2.83 g of polymer-bound triphenylphosphine (loading=3.0 mmol/g), 2,4-difluorobenzyl alcohol (0.980 g, 6.80 mmol), followed by di-tert-butylaziocarboxylate (1.57 g, 6.80 mmol). After 5 min. the cooling bath was removed. The resulting mixture was stirred for 1.5 h. and then trifluoroacetic acid (10 mL) was added. After 1 h. the reaction mixture was filtered through a pad of Celite® and washed with dichloromethane. The filtrate was concentrated then suspended in H₂O (50 mL) and made alkaline with 1.0 N NaOH. The aqueous reaction was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over Na₂SO₄, filtered and concentrated. The residue was dissolved in methanol, absorbed onto silica gel and subjected to chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) to provide a white solid (0.250 g, 17%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.75 (d, J=8.3 Hz, 2H), 7.60 (app q, J=7.9 Hz, 1H), 7.32-7.30 (m, 1H), 7.27-7.23 (m, 1H), 7.24 (app d, J=8.3 Hz, 2H), 7.12 (app dt, J=1.9, 8.3 Hz, 1H), 5.95 (s, 2H), 5.26 (s, 2H), 5.07 (s, 2H), 2.16 (s, 3H).

Step 3. Preparation of 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzenesulfonamide. 4-{[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzenesulfonamide (Step 2) (0.270 g, 0.523 mmol) was suspended in acetonitrile (3.0 mL). N-Bromosuccinimide (0.098 g, 0.549 mmol) was added and the resulting mixture was stirred at room temperature for 1 h., at which time the reaction mixture was concentrated. Chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) provided a white solid (0.210 g, 81%). ¹H NMR (400 MHz, CDCl₃) δ 7.76 (d, J=8.5 Hz, 2H), 7.64 (app q, J=7.9 Hz, 1H), 7.34-7.29 (m, 1H), 7.25 (d, J=8.5 Hz, 2H), 7.16 (app dt, J=2.4, 8.5 Hz, 1H), 6.57 (s, 1H), 5.35 (s, 2H), 5.28 (s, 2H), 2.28 (s, 3H). ES-HRMS m/z 499.0160 (M+H calcd for C₂₀H₁₈BrF₂N₂O₄S requires 499.0133).

Example 761

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N-methylurea

Preparation of N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2oxopyridin 1(2H)-yl]methyl}benzyl)-N-methylurea. The product from Example 208 (0.300 g, 0.648 mmol) was suspended in tetrahydrofuran (3.0 mL). 4-methylmorpholine (0.142 mL, 1.30 mmol) and trimethylsilylisocyanate (0.176 mL, 1.30 mmol) were added and the resulting mixture was stirred at room temperature for 2 days at which time additional trimethylsilylisocyanate (0.176 mL, 1.30 mmol) was added. The resulting reaction mixture was stirred at room temperature for 24 h. and then heated to 40° C. for 2 h. at which time the reaction was concentrated. The residue was absorbed onto silica gel and subjected to chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) to give the title compound as a white solid (0.147 g, 45%). ¹H NMR (400 MHz, CDCl₃) δ 7.63 (app q, J=7.9 Hz, 1H), 7.31 (dt, J=2.5, 9.9 Hz, 1H), 7.17-7.12 (app m, 1H), 7.13 (app d, J=8.2 Hz, 2H), 7.03 (d, J=8.1 Hz, 2H), 6.53 (s, 1H), 5.88 (s, 2H), 5.26 (s, 4H), 4.33 (s, 2H), 2.68 (s, 3H), 2.28 (s, 3H). ES-HRMS m/z 506.0898 (M+H calcd for C₂₃H₂₃BrF₂N₃O₃ requires 506.0885).

Example 762

5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyridine-2-carboxamide

Step 1. Preparation of 2-iodo-5-(iodomethyl)pyridine

5-Hydroxymethyl-2-chloropyridine (20.3 g, 141.4 mmol) was dissolved in acetonitrile (250 mL). Sodium iodide (74.2 g, 494.9 mmol) and acetyl chloride (35.2 mL, 494.9 mmol) were added and the resulting mixture was heated at reflux for 24 h. The reaction mixture was cooled in an ice-bath and the solids were collected by filtration washing with acetonitrile. The solids were then suspended in H₂O and treated with K₂CO₃ (pH-8). The resulting solids were collected by filtration washing with diethyl ether and dichloromethane to provide a pale yellow solid (5.70 g, 12%). LC/MS, t_r=2.47 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 346(M+H).

Step 2. Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(6-iodopyridin-3-yl)methyl]-6-methylpyridin-2(1H)-one

2-Iodo-5-(iodomethyl)pyridine (Step 1) (3.00 g, 8.70 mmol) and the product from Example 734 (1.91 g, 5.80 mmol) were suspended in tetrahydrofuran (15 mL) and N,N-dimethylformamide (5.0 mL). Sodium hydride (0.510 g, 12.76 mmol, 60% dispersion in mineral oil) was added at room temperature. The resulting mixture was heated to 60° C. for 15 h. and then allowed to cool to room temperature. Additional 2-iodo-5-(iodomethyl)pyridine (1.00 g, 2.90 mmol) and sodium hydride (0.232 g, 5.80 mmol, 60% dispersion in mineral oil) were added and the resulting mixture was heated to 60° C. for 2 h. After cooling to room temperature the reaction was diluted with H₂O and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered and concentrated. The resulting solid was washed with diethyl ether to give a brown solid (2.32 g, 73%). ¹H NMR (400 MHz, CDCl) δ 8.23 (d, J=2.3 Hz, 1H), 7.77 (d, J=8.1 Hz, 1H), 7.62 (q, J=7.9 Hz, 1H), 7.30 (dt, J=2.4, 9.9 Hz, 1H), 7.20 (app dt, J=2.4, 8.1 Hz, 1H), 7.14 (app dt, J=1.8, 8.3 Hz, 1H), 6.56 (s, 1H), 5.26 (s, 2H), 5.23 (s, 2H), 2.32 (s, 3H).

Step 3. Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyridine-2-carbonitrile

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(6-iodopyridin-3-yl)methyl]-6-methylpyridin-2(1H)-one (from Step 2) (1.50 g, 2.74 mmol) was dissolved in N,N-dimethylformamide (6.0 mL). Zinc cyanide (0.193 g, 1.64 mmol) and tetrakis(triphenylphosphine)palladium (0) (0.317 g, 0.274 mmol) were added and the resulting mixture was heated to 80° C. for 16 h. and then cooled to room temperature. The reaction was diluted with H₂O and 2M NH₄OH (30 mL). The aqueous reaction mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na₂SO₄, filtered and concentrated. Chromatography (silica gel, hexanes/ethyl acetate with 10% methanol) provided a pale yellow solid (0.700 g, 57%). %). ¹H NMR (400 MHz, CDCl₃) δ 8.61 (d, J=1.6 Hz, 1H), 7.96 (d, J=8.3 Hz, 1H), 7.69-7.66 (m, 1H), 7.65-7.60 (m, 1H), 7.30 (app dt, J=2.4, 9.9 Hz, 1H), 7.14 (app dt, J=1.7, 8.5 Hz, 1H), 6.59 (s, 1H), 5.38 (s, 2H), 5.27 (s, 2H), 2.32 (s, 3H).

Step 4. Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyridine-2-carboxamide. 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyridine-2-carbonitrile (from Step 3) (0.300 g, 0.672 mmol) was suspended in tetrahydrofuran (3.0 mL). Potassium trimethylsilanolate (0.172 g, 1.34 mmol) was added and the resulting mixture was stirred at room temperature for 23 h. H₂O was added and the tetrahydrofuran was removed by blowing N₂ over the reaction mixture. The solids were collected by filtration to provide the title compound as a tan solid (0.225 g, 72%). ¹H NMR (400 MHz, CDCl₃) δ 8.47 (d, J=1.7 Hz, 1H), 8.04 (br s, 1H), 7.96 (d, J=8.2 Hz, 1H), 7.67-7.60 (m, 2H), 7.31 (app dt, J=2.5, 9.9 Hz, 1H), 7.14 (app dt, J=1.7, 8.5 Hz, 1H), 6.58 (s, 1H), 5.38 (s, 2H), 5.27 (s, 2H), 2.32 (s, 3H). ES-HRMS m/z 464.0416 (M+H calcd for C₂₀H₁₇BrF₂N₃O₃ requires 464.0436).

Example 763

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-hydroxypropanamide

To a reaction vessel (borosilicate culture tube) was added the product from Example 704 (0.332 g, 0.604 mmol) and methanol (2.0 mL) followed by a saturated solution of K₂CO₃ (1 mL). The reaction was stirred for 1 h. at room temperature. The reaction mixture was then extracted with ethyl acetate (3×10 mL). The combined organics were washed with brine (15 mL), dried with Na₂SO₄, and concentrated to afford an off-white solid (0.264 g, 86%). ¹H NMR (400 MHz, DMF-d₆) δ 7.79-7.73 (m, 3H), 7.30 (ddd, J=2.55, 9.40, 10.47 Hz, 1H), 7.21-7.17 (m, 3H), 6.61 (s, 1H), 5.37 (s, 4H), 4.22 (q, J=6.76 Hz, 1H), 2.41 (s, 3H), 1.35 (d, J=6.71 Hz, 3H). ES-HRMS m/z 507.0721 (M+H calcd for C₂₃H₂ BrF₂N₂O₄ requires 507.0726).

Example 764

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-hydroxy-2-methylpropanamide

By following the method of Example 763 and substituting the compound from Example 704 with the compound from Example 705, the title compound was prepared (0.293 g, 95%). ¹H NMR (400 MHz, DMF-d₆) δ 9.58 (s, 1H), 7.81-7.74 (m, 3H), 7.33-7.17 (m, 4H), 6.61 (s, 1H), 5.78 (s, 1H), 5.38 (s, 4H), 2.41 (s, 3H), 1.39 (s, 6H). ES-HRMS m/z 521.0880 (M+H calcd for C₂₄H₂₃BrF₂N₂O₄ requires 521.0882).

Example 765

N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)urea

To a reaction vessel (borosilicate culture tube) was added the compound from Example 611 (0.500 g, 1.149 mmol) and tetrahydrofuran (10.0 mL) followed by N-methylmorpholine (0.232 g, 2.298 mmol) and trimethylsilyl isocynate (0.199 g, 1.724 mmol). The reaction was stirred for 20 days at room temperature. The reaction mixture was then diluted with tetrahydrofuran and the solids collected by filtration. The filtrate was concentrated and purified by chromatography (silica gel, hexaneethyl acetate containing 10% methanol). The two solids were combined to afford a white solid (0.140 g, 25%). ¹H NMR (400 MHz, DMF-d₆) δ 8.78 (s, 1H), 7.75 (app q, J=7.83 Hz, 1H), 7.46 (app d, J=8.59 Hz, 2H), 7.31 (ddd, J=2.55, 10.61, 11.95 Hz, 1H), 7.28-7.08 (m, 3H), 6.59 (s, 1H), 5.93 (s, 2H), 5.36 (s, 2H), 5.33 (s, 2H), 2.41 (s, 3H). ES-HRMS m/z 478.0571 (M+H calcd for C₂₁H₁₈BrF₂N₃O₃ requires 478.0572).

Example 766

3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide

Step 1: Preparation of the title compound. {1-[3-(aminocarbonyl)phenyl]-5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate (1.09 g, 2.36 mmol) was dissolved in methanol (10 mL) and K₂CO₃ (0.69 g, 5.19 mmol) was added. H₂O (1 mL) was added and the reaction mixture was stirred at room temperature for 1 h. The reaction was then diluted with H₂O (30 mL) and the precipitate was collected by filtration washing with H₂O (3×20 mL) to afford a tan solid (0.820 g, 83%). ¹H NMR (400 MHz, DMF-d₆) δ 8.21 (br s, 1H), 8.09 (d, J=7.79 Hz, 1H), 7.90 (s, 1H), 7.78 (app dt, J=6.71, 8.45 Hz, 1H) 7.67-7.56 (m, 2H), 7.46 (br s, 1H), 7.34 (ddd, J=2.55, 9.53, 10.34 Hz, 1H), 7.24-7.19 (m, 1H), 6.83 (s, 1H), 5.85 (s, 2H), 4.10 (AB q, J_AB=15.04 Hz, 2H). ES-HRMS m/z 421.0766 (M+H calcd for C₂₀H₁₅ClF₂N₂O₄ requires 421.0761).

Example 767

{1-[3-(aminocarbonyl)phenyl]-5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl Carbamate

Step 1: Preparation of the title compound. 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide (0.350 g, 0.832 mmol) was suspended in tetrahydrofuran (3 mL) and trichloroacetyl chloride (0.170 g, 0.902 mmol) was added. The reaction mixture was stirred at room temperature for 1.5 h. Al₂O₃ (2.11 g, 20.75 mmol) was added followed by tetrahydrofuran (3 mL) and the reaction was stirred for 1.5 h. at room temperature. The reaction was then heated to reflux for 1 h. The reaction mixture was then filtered through Celite®, washed with methanol, and the filtrate concentrated. The resulting residue was dissolved in 1,4-dioxane (5 mL) and Al₂O₃ (2.11 g, 20.75 mmol) was added. The reaction mixture was refluxed for 1 h., filtered through Celite®, washed with methanol, and the filtrate concentrated. The resulting residue was tritrated with diethyl ether to afford a white solid (0.195 g, 51%). ¹H NMR (400 MHz, DMF-d₆) δ 8.18 (br s, 1H), 8.11 (d, J=7.79 Hz, 1H), 7.93 (s, 1H), 7.81 (app dt, J=6.58, 8.59 Hz, 1H) 7.67-7.58 (m, 2H), 7.46 (br s, 1H), 7.34 (ddd, J=2.55, 9.53, 10.61 Hz, 1H), 7.24-7.20 (m, 1H), 6.87 (s, 1H), 5.45 (s, 2H), 4.58 (AB q, J_AB=15.98 Hz, 2H). ES-HRMS m/z 464.0842 (M+H calcd for C₂₁H₁₆ClF₂N₃O₅ requires 464.0819).

Example 768

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide

Step 1: Preparation of Methyl 3-[6-[(acetyloxy)methyl]-4-hydroxy-2-oxopyridin-1(2H)-yl]benzoate

3-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-2-oxopropyl acetate (from Example 653, step 1) (12.25 g, 50.57 mmol) was dissolved in 1,4-dioxane (300 mL) and methyl 3-aminobenzoate (5.88 g, 38.90 mmol) was added. The reaction was heated to reflux for 1 h. then cooled to 70° C. Methanesulfonic acid (3.74 g, 38.90 mmol) was added and the reaction brought back to reflux for 1 h. The reaction was cooled to room temperature, concentrated and used as crude product for the next step.

Step 2: Preparation of Methyl 3-[6-[(acetyloxy)methyl]-3-bromo-4-hydroxy-2-oxopyridin-1(2H)-yl]benzoate

Methyl 3-[6-[(acetyloxy)methyl]-4-hydroxy-2-oxopyridin-1(2H)-yl]benzoate (crude from step 1) (12.34 g, 38.90 mmol) dissolved in acetonitrile (110 mL) was cooled in an ice-bath. N-bromosuccinimide (7.27 g, 40.85 mmol) was added and the ice-bath was removed. The reaction mixture was stirred for 1 h. at room temperature. The reaction was diluted with diethyl ether and the solids collected by filtration. The solid was then washed with diethyl ether (3×50 mL) to afford a tan solid (8.38 g, 54% over two steps). ¹H NMR (400 MHz, DMSO-d₆) δ 8.01 (app dt, J=1.48, 7.92 Hz, 1H), 7.81 (app t, J=1.68 Hz, 1H), 7.66-7.59 (m, 2H), 6.29 (s, 1H), 4.49 (AB q, J_AB=14.97 Hz, 2H), 3.84 (s, 3H), 1.88 (s, 3H). ES-HRMS m/z 396.0118 (M+H calcd for C₁₆H₁₄BrNO₆ requires 396.0077).

Step 3: Preparation of Methyl 3-[6-[(acetyloxy)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzoate

Methyl 3-[6-[(acetyloxy)methyl]-3-bromo-4-hydroxy-2-oxopyridin-1(2H)-yl]benzoate (from step 2) (8.30 g, 20.95 mmol) was dissolved in N,N-dimethylformamide (42 mL). K₂CO₃ (3.08 g, 23.05 mmol) was added followed by 2,4-difluorobenzyl bromide (5.64 g, 27.24 mmol). The reaction mixture was stirred for 24 h. at room temperature. The reaction mixture was then diluted with diethyl ether and the solids collected by filtration. The solid was then washed with H₂0 (3×50 mL) to afford a white solid (8.81 g, 80%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.03 (d, J=7.52 Hz, 1H), 7.85 (s, 1H), 7.70-7.60 (m, 3H), 7.33 (ddd, J=2.55, 8.32, 10.88 Hz, 1H), 7.16 (app dt, J=1.61, 7.79 Hz, 1H), 6.83 (s, 1H), 5.37 (s, 2H), 4.57 (AB q, J_AB=15.44 Hz, 2H), 3.85 (s, 3H), 1.88 (s, 3H). ES-HRMS m/z 522.0388 (M+H calcd for C₂₃H₁₉BrF₂NO₆ requires 522.0358).

Step 4: Preparation of Methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzoate

Methyl 3-[6-[(acetyloxy)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzoate (from step 3) (15.50 g, 29.68 mmol) was dissolved in methanol (120 mL) and K₂CO₃ (8.72 g, 65.29 mmol) was added. The reaction mixture was stirred for 1 h. at room temperature and diluted with H₂O. The solids were collected by filtration and washed with H₂O (3×50 mL) to afford a white solid (13.24 g, 93%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.03 (app dt, J=1.21, 7.65 Hz, 1H), 7.81 (app t, J=1.88 Hz, 1H), 7.67-7.57 (m, 3H), 7.34 (app t, J=1.28 Hz, 1H), 7.16 (app t, J=1.28 Hz, 1H), 6.66 (s, 1H), 5.62 (app t, J=5.37 Hz, 1H), 5.35 (s, 2H), 3.88 (app t, J=5.17 Hz, 2H), 3.84 (s, 3H). ES-HRMS m/z 480.0258 (M+H calcd for C₂₁H₁₆BrF₂NO₅ requires 480.0253).

Step 5: Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzoic Acid

Methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzoate (from step 4) (5.00 g, 10.41 mmol) was dissolved in tetrahydrofuranmethanol (3.5:1) (21 mL). 4N NaOH (6.5 mL, 26.03 mmol) was added and the reaction mixture was stirred for 1 h. at room temperature. The reaction was acidified (pH 2) with 4N HCl and the solids collected by filtration washing with H₂O (3×50 mL) to afford a white solid (4.54 g, 93%). ¹H NMR (400 MHz, DMF-d₆) δ 8.29 (app dt, J=1.61, 7.38 Hz, 1H), 8.11 (app t, J=1.54 Hz, 1H), 7.99-7.82 (m, 3H), 7.49 (ddd, J=1.21, 9.40, 10.61 Hz, 1H), 7.38 (ddd, J=2.55, 9.53, 10.61 Hz, 1H), 6.97 (s, 1H), 5.95 (s, 1H), 5.63 (s, 2H), 4.26 (s, 2H). ES-HRMS m/z 466.0097 (M+H calcd for C₂₀H₁₄BrF₂NO₅ requires 466.0096).

Step 6: Preparation of the title compound. 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzoic acid (from step 5) (0.200 g, 0.429 mmol) was suspended in tetrahydrofuran (2 m]L). 2-Chloro-4,6-dimethoxy-1,3,5-triazine (0.090 g, 0.515 mmol) was added followed by N-methylmorpholine (0.130 g, 1.287 mmol). The reaction mixture was stirred at room temperature for 1.5 h. Reagent grade NH₄OH (1 mL) was added and the reaction was stirred overnight at room temperature. The reaction was then diluted with H₂O (50 mL) and the precipitate was collected by filtration washing with diethyl ether (3×20 mL) to afford a white solid (0.184 g, 93%). ¹H NMR (400 MHz, DMF-d₆) δ 8.20 (br s, 1H), 8.09 (app dt, J=1.41, 8.05 Hz, 1H), 7.89 (t, J=1.74 Hz, 1H), 7.78 (app dt, J=6.58, 8.59 Hz, 1H) 7.65 (t, J=7.85 Hz, 1H), 7.58-7.55 (m, 1H), 7.46 (br s, 1H), 7.34 (ddd, J=2.55, 9.26, 10.47 Hz, 1H), 7.22 (ddd, J=1.16, 8.46, 10.34 Hz, 1H), 6.80 (s, 1H), 5.80 (br s, 1H), 5.47 (s, 2H), 4.08 (s, 2H). ES-HRMS m/z 465.0234 (M+H calcd for C₂₀H₁₅BrF₂N₂O₄ requires 465.0256).

Example 769

{1-[3-(aminocarbonyl)phenyl]-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl Acetate

Step 1: Preparation of the title compound. 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide (from Example 768, above) (0.300 g, 0.643 mmol) was suspended in pyridine (3 mL) and acetic anhydride (0.099 g, 0.965 mmol) was added. The reaction mixture was stirred at room temperature overnight. The reaction was then diluted with H₂O (50 mL) and the precipitate was collected by filtration washing with H₂O (2×30 mL) followed by diethyl ether (3×30 mL) to afford a white solid (0.251 g, 77%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.02 (br s, 1H), 7.95 (app d, J=7.79 Hz, 1H), 7.75 (app d, J=1.75 Hz, 1H), 7.67 (app q, J=8.01 Hz, 1H), 7.48-7.15 (m, SH), 6.82 (s, 1H), 5.38 (s, 2H), 4.58 (AB q, J_AB=15.35 Hz, 2H), 1.89 (s, 3H). ES-HRMS m/z 507.0389 (M+H calcd for C₂₂H₁₇BrF₂N₂O₅ requires 507.0362).

Example 770

{1-[3-(aminocarbonyl)phenyl]-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl Carbamate

Step 1: Preparation of the title compound. 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide (from Example 768, above) (0.300 g, 0.643 mmol) was suspended in tetrahydrofuran (3 mL) and trichloroacetyl chloride (0.133 g, 0.707 mmol) was added. The reaction mixture was stirred at room temperature 1.5 h. Reagent grade NH₄OH (1.5 mL) was added and the reaction was stirred overnight at room temperature. The reaction was then diluted with H₂O (50 mL) and the precipitate was collected by filtration washing with H₂O (2×30 mL) followed by diethyl ether (3×30 mL) to afford a white solid (0.255 g, 78%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.00 (br s, 1H), 7.96 (app d, J=7.92 Hz, 1H), 7.72 (m, 2H), 7.58 (app t, J=7.79 Hz, 1H), 7.47-7.15 (m, 4H), 6.72 (s, 1H), 5.35 (s, 2H), 4.43 (AB q, J_AB=18.12 Hz, 2H). ES-HRMS m/z 508.0328 (M+H calcd for C₂₁H₁₆BrF₂N₃O₅ requires 508.0314).

Example 771

3-[6-(aminomethyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzamide Hydrochloride

Step 1: Preparation of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-2-oxopyridin-1(2H)-yl]benzamide

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide (from Example 768, above) (4.00 g, 8.60 mmol), triphenylphosphine (4.96 g, 18.91 mmol), and phthalimide (1.39 g, 9.46 mmol) dissolved in tetrahydrofuran/1-methyl-2-pyrrolidinone (1:1) (34.4 mL) were cooled in an ice bath. Diethyl azodicarboxylate (3.29 g, 18.91 mmol) was added and the ice bath removed. The reaction mixture was stirred at room temperature 1.5 h. The reaction was then diluted with ethyl acetate (75 mL) and the organic washed with H₂O (2×50 mL), 1N HCl (2×50 mL), saturated NaHCO₃ (2×50 mL), brine (50 mL), dried with Na₂SO₄, and concentrated. The resulting residue was tritrated with dichloromethane to afford an off-white solid (3.19 g, 62%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.98-7.79 (m, 7H), 7.60-7.49 (m, 3H), 7.42 (s, 1H), 7.17 (app dt, J=2.55, 9.53 Hz, 1H), 7.07 (app dt, J=2.55, 8.46 Hz, 1H), 6.45 (s, 1H), 5.28 (s, 2H), 4.24 (AB q, J_AB=21.08 Hz, 2H). ES-HRMS m/z 594.0477 (M+H calcd for C₂₈H₁₈BrF₂N₃O₅ requires 594.0471).

Step 2: Preparation of the title compound. 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-2-oxopyridin-1(2H)-yl]benzamide (from step 1) (3.92 g, 6.59 mmol) was suspended in 1,4-dioxane (22 mL). Hydrazine (0.660 g, 13.191 mmol) was added and the reaction mixture was stirred at reflux for 4 h. The reaction was cooled to room temperature and the resulting solids collected by filtration. The impure solid was suspended in 1,4-dioxane (50 mL) and 1N NaOH (20 mL) and was stirred at room temperature for 1 h. The solids were filtered and washed with 1,4-dioxane (2×25 mL) and H₂O (2×25 mL). The filtrate was diluted with ethyl acetate (100 mL) and washed with H₂O (25 mL), brine (25 mL), dried with Na₂SO₄, and concentrated. The two solids were combined and washed with diethyl ether (3×30 mL) to afford an off-white solid (1.86 g, 61%). ¹H NMR (400 MHz, DMF-d₆) δ 9.35 (br s, 2H), 8.31 (br s, 1H), 8.11-8.08 (m, 2H), 7.89 (app q, J=7.88 Hz, 21), 7.70-7.64 (m, 2H), 7.53 (s, 1H), 7.47 (br s, 1H), 7.36-7.31 (m, 1H), 7.22-7.18 (m, 1H), 5.52 (s, 2H), 3.96 (s, 2H). ES-HRMS t/z 464.0427 (M+H calcd for C₂₀H₁₆BrF₂N₃O₃ requires 464.0416).

Example 772

5-[[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-yl]methyl]-1,3-dihydro-2H-indol-2-one

Step 1: Preparation of 3,3-dibromo-5-[[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-yl]methyl]-1,3-dihydroindol-2-one

3-Chloro-4-(2,4-difluorobenzyloxy)-1(1H-indol-5-ylmethyl)-pyridin-2(1H)-one (1.2 g, 3.0 mmol) was diluted with 25 mL of t-BuOH and pyridinium bromide perbromide (2.51 g, 7.83 mmol) was added portion-wise over a period of 20 min. The reaction was stirred at room temperature for 16.5 h. The reaction was evaporated on a rotary evaporator, and the resulting solid dissolved in water, extracted with EtOAc, dried (Na₂SO₄), filtered, and concentrated under reduced pressure to give a dark, tan solid (1.37 g, 87%), which was carried forward without further purification or analysis.

Step 2. Preparation of title compound. 3,3-Dibromo-5-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]-1,3-dihydroindol-2-one (1.75 g, 3.04 mmol) and zinc dust (1.98 g, 30.4 mmol) was diluted with 60 mL acetic acid, and the reaction was stirred at room temperature for 17.5 h. The reaction was diluted with water, extracted with EtOAc, washed with brine, dried (Na₂SO₄), filtered and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 95:5 CH₂Cl₂/MeOH) gave a tan solid (0.10 g, 9%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.38 (s, 1H), 7.92 (d, J=8 Hz, 1H), 7.62 (app q, J=9 Hz, 1H), 7.33 (app t, J=9 Hz, 1H), 7.19-7.13 (m, 3H), 6.76 (d, J=9 Hz, 1H), 6.59 (d, J=8 Hz, 1H), 5.29 (s, 2H), 5.04 (s, 2H), 3.45 (s, 2H). ES-HRMS m/z 417.0823 (M+H calcd for C₂₁H₁₆ClF₂N₂O₃ requires 417.0812).

Example 773

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(1H-pyrazol-3-ylmethyl)-pyridin-2(1H)-one

Step 1. Preparation of the title compound. 3-Chloro-4-(2,4-difluorobenzyloxy)-pryidin-2(1H)-one (see Example 80) (1.9 g, 6.9 mmol) and K₂CO₃ (1.9 g, 13.8 mmol) were stirred in 60 mL of anhydrous DMF, and 3-bromomethyl-pyrazole-1-carboxylic acid tert-butyl ester (2.2 mL, 8.3 mmol) was added dropwise. The reaction was stirred at 80° C. for 15.5 h. The reaction was cooled to room temperature and diluted with brine, extracted with EtOAc, washed with 5% LiCl, brine, dried (Na₂SO₄), filtered and evaporated on a rotary evaporator. Purification by preparatory HPLC (Phenomenex Luna 10μ, C18(2) 250×21.2 mm) provided a white solid (0.30 g, 10%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.80 (d, J=7.8 Hz, 1H), 7.66-7.58 (m, 2H), 7.34 (app t, J=7.8 Hz, 1H), 7.16 (app t, J=8.5 Hz, 1H), 6.57 (d, J=7.7 Hz, 1H), 6.15 (s, 1H), 5.29 (s, 2H), 5.10 (s, 2H), 2.07 (s, 1H). ES-HRMS m/z 352.0661 (M+H calcd for C₁₆H₁₃ClF₂N₃O₂ requires 352.0659).

Example 774

3-Bromo-4-(2,4-difluorobenzyloxy)-1-(1H-pyrazol-3-ylmethyl)-pyridin-2(1H)-one

Step 1. Preparation of 3-bromo-4-(2,4-difluorobenzyloxy)-pyridin-2(1H)-one

4-(2,4-Difluorobenzyloxy)-pyridin-2(1H)-one (see Example 74) (2.4 g, 10.2 mmol) was dissolved in 19 ml of acetic acid, cooled to 0° C., and bromine (0.53 mL, 10.3 mmol) in 34 mL acetic acid was added dropwise. The reaction was stirred at room temperature for 2 h. The reaction was evaporated on a rotary evaporator. The resulting solid was recrystallized from EtOAc and hexanes to give a white solid (3.3 g, 100%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.62 (app q, J=6.7 Hz, 1H), 7.50 (d, J=7.4 Hz, 1H), 7.34 (dt, J=10.4, 2.5 Hz, 1H), 7.17 (dt, J=8.6, 2.3 Hz, 1H), 6.44 (d, J=7.4 Hz, 1H), 5.29 (s, 2H).

Step 2. Preparation of 3-[3-bromo-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]pyrazole-1-carboxylic Acid Tert-Butyl Ester

3-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]pyrazole-1-carboxylic acid tert-butyl ester was prepared by a procedure similar to the one described for Example 74 (Step 4) to provide a white solid (1.3 g, 21%): ¹H NMR (300 MHz, DMSO-d₆) δ 8.19 (d, J=2.7 Hz, 1H), 7.93 (d, J=7.7 Hz, 1H), 7.64 (app q, J=6.8 Hz, 1H), 7.34 (dt, J=10.4, 2.5 Hz, 1H), 7.17 (dt, J=8.6, 2.3 Hz, 1H), 6.59 (d, J=7.8 Hz, 1H), 6.39 (d, J=2.7 Hz, 1H), 5.31 (s, 2H), 5.16 (s, 2H), 1.56 (s, 9H). HRMS m/z 497 (M+H).

Step 3. Preparation of the title compound. 3-[3-Bromo-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]pyrazole-1-carboxylic acid tert-butyl ester (1.2 g, 2.5 mmol) was heated to 130° C. for 16 h. The reaction was cooled to room temperature and partitioned between water and ethyl acetate. The separated organic layer was washed with brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator to give an off-white solid. Trituration from methanol provided a white solid (0.59 g, 60%): ¹H NMR (300 MHz, DMSO-d₆) δ 12.73 (br s, 1H), 7.83 (d, J=7.7 Hz, 1H), 7.66-7.59 (m, 2H), 7.34 (dt, J=12.8, 2.5 Hz, 1H), 7.16 (dt, J=8.5, 2.4 Hz, 1H), 6.52 (d, J=7.7 Hz, 1H), 6.15 (s, 1H), 5.29 (s, 2H), 5.11 (s, 2H). ES-HRMS m/z 396.0172 (M+H calcd for C₂₁H₁₃BrF₂N₃O₂ requires 396.0153).

Example 775

3-Chloro-4-(2,4-difluorobenzyloxy)-1-[1-(2-hydroxyethyl)-1H-pyrazol-3-ylmethyl]-6-methyl-pyridin-2(1H)-one

Step 1. Preparation of the title compound. 3-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]pyrazole (0.53 mg, 1.5 mmol), 2N NaOH (1.5 mL, 2.9 mmol), benzyltriethylammonium chloride (0.17 g, 0.72 mmol), sodium iodide (10 mg), and 2-chloroethanol (0.15 mL, 2.2 mmol) were stirred in 5 mL of 1,4-dioxane at 85° C. for 19 h. The reaction was cooled to room temperature, neutralized with 1N HCl, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:9 MeOH/chloroform) provided a white solid (0.11 g, 19%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.65-7.60 (m, 2H), 7.34 (dt, J=10.4, 2.5 Hz, 1H), 7.17 (dt, J=8.5, 1.7 Hz, 1H), 6.52 (s, 1H), 6.05 (d, J=2.2 Hz, 1H), 5.27 (s, 2H), 5.16 (s, 2H), 4.85 (t, J=5.3 Hz, 1H), 4.06 (t, J=5.6 Hz, 2H), 3.67 (q, J=5.5 Hz, 2H), 2.50 (s, 3H). ES-HRMS m/z 410.1065 (M+H calcd for C₁₉H₁₉ClF₂N₃O₃ requires 410.1078).

Example 776

1-Benzooxazol-6-ylmethyl-3-chloro-4-(2,4-difluorobenzyloxy)-6-methyl-pyridin-2(1H)-one

Step 1. Preparation of 6-bromomethylbenzooxazole

6-Methylbenzoxazole (2.5 g, 19 mmol), N-bromosuccinimide (3.7 g, 21 mmol) and benzoyl peroxide (50 mg) were dissolved in 32 mL of carbon tetrachloride. The reaction was stirred at reflux for 6 h. The reaction was cooled to room temperature, filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:3 EtOAc/hexanes) gave a light yellow oil (1.1 g, 28%): ¹H NMR (300 MHz, CDCl₃) δ 8.12 (s, 1H), 7.76 (d, J=9.0 Hz, 1H), 7.64 (d, J=1.5 Hz, 1H), 7.42 (dd, J=8.1, 1.5 Hz, 1H), 4.63 (s, 2H).

Step 2. Preparation of the title compound. 1-Benzooxazol-6-ylmethyl-3-chloro-4-(2,4-difluorobenzyloxy)-6-methyl-pyridin-2(1H)-one was prepared by a procedure similar to the one described for Example 777 (below) to provide an off-white solid (0.75 g, 50%): ¹H NMR (300 MHz, DMSO-d₆) δ 8.73 (s, 1H), 7.77 (d, J=8.2 Hz, 1H), 7.67 (app q, J=8.6 Hz, 1H), 7.52 (br s, 1H), 7.36 (dt, J=10.4, 2.5 Hz, 1H), 7.21-7.15 (m, 2H), 6.62 (s, 1H), 5.45 (s, 2H), 5.30 (s, 2H), 2.35 (s, 3H). ES-HRMS m/z 417.0812 (M+H calcd for C₂₁H₁₆ClF₂N₂O₃ requires 417.0794).

Example 777

3-Bromo-4-(2,4-difluorobenzyloxy)-6-methyl-1-(1H-pyrazol-3-ylmethyl)-pyridin-2(1H)-one

Step 1. Preparation of 3-[3-bromo-4-(2,4-difluoro-benzylozy)-6-methyl-2-oxo-pyridin-1(2H)-ylmethyl]-pyrazole-1-carboxylic Acid Tert-Butyl Ester

3-Bromo-4-(2,4-difluorobenzyloxy)-6-methyl-1H-pyridin-2-one (3.72 g, 11.3 mmol) was diluted with 80 mL of THF, cooled to 0° C., and NaH (0.90 g, 22.5 mmol) was added portionwise over a period of 30 min. The reaction was warmed to room temperature, and 3-bromomethyl-pyrazole-1-carboxylic acid tert-butyl ester (4.41 g, 16.9 mmol) was added to the reaction. The reaction was stirred at 70° C. for 16 h. The reaction was quenched with a saturated solution of NH₄Cl and diluted with EtOAc. The organic layer was washed with brine, dried (Mg₂SO₄), filtered and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:1 EtOAc/hexanes) provided a light yellow solid (1.94 g, 34%): ¹H NMR (300 MHz, DMSO-d₆) δ 8.17 (d, J=2.7 Hz, 1H), 7.65 (app q, J=8.5 Hz, 1H), 7.34 (app t, J=8.0, 1H), 7.17 (app t, J=8.2 Hz, 1H), 6.56 (s, 1H), 6.35 (d, J=2.7 Hz, 1H), 5.29 (s, 2H), 5.25 (s, 2H), 2.45 (s, 3H), 1.55 (s, 9H).

Step 2. Preparation of the title compound. 3-[3-Bromo-4-(2,4-difluoro-benzylozy)-6-methyl-2-oxo-pyridin-1(2H)-ylmethyl]-pyrazole-1-carboxylic acid tert-butyl ester (1.94 g, 3.81 mmol), was diluted in 15 mL of anhydrous DMSO and stirred at reflux for 17 h. The reaction was cooled to room temperature and partitioned between water and EtOAc. The aqueous layer was extracted 3 times with EtOAc, dried (Mg₂SO₄), filtered, and evaporated on a rotary evaporator. The reaction was diluted with EtOAc and hexanes. The solid was filtered to provide a tan solid (1.13 g, 75%): ¹H NMR (300 MHz, DMSO-d₆) δ 12.67 (br s, 1H), 7.68-7.60 (m, 2H), 7.34 (app t, J=9 Hz, 1H), 7.17 (app t, J=9 Hz, 1H), 6.49 (s, 1H), 6.11 (s, 1H), 5.27 (s, 2H), 5.21 (s, 2H), 2.49 (s, 3H). ES-HRMS m/z 410.0295 (M+H calcd for C₁₇H₁₅BrF₂N₃O₂ requires 410.0313).

Example 778

3-Chloro-4-(2,4-difluorobenzyloxy)-1-[1-(2-methoxyacetyl)-1H-pyrazol-3-ylmethyl]-6-methyl-pyridin-2(1H)-one

Step 1. Preparation of the title compound. 3-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]pyrazole (0.25 mg, 0.68 mmol), NMM (0.15 mL, 1.4 mmol), and methoxyacetyl chloride (0.07 mL, 0.75 mmol) were stirred in 5 mL of THF for 14 h. The solid was filtered, and washed with water. The solid was dried in a vacuum oven overnight to provide a white solid (0.19 g, 64%): ¹H NMR (300 MHz, DMSO-d₆) δ 8.35 (d, J=2.8 Hz, 1H), 7.65 (app q, J=6.7 Hz, 1H), 7.34 (dt, J=10.3, 2.5 Hz, 1H), 7.19 (dt, J=8.5, 2.0 Hz, 1H), 6.60 (s, 1H), 6.46 (d, J=2.8 Hz, 1H), 5.29 (s, 2H), 5.26 (s, 2H), 4.78 (s, 2H), 3.39 (s, 3H), 2.48 (s, 3H). ES-HRMS m/z 438.1043 (M+H calcd for C₂₀H₁₉ClF₂N₃O₀ requires 438.1027).

Example 779

3-Chloro-1-(1-cyclopropanecarbonyl-1H-pyrazol-3-ylmethyl)-4-(2,4-difluorobenzyloxy)-6-methyl-pyridin-2(1H)-one

Step 1. Preparation of the title compound. 3-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]pyrazole (0.18 mg, 0.49 mmol), NMM (0.11 mL, 0.98 mmol), and cyclopropanecarbonyl chloride (0.05 mL, 0.54 mmol) were stirred in 5 mL of THF for 14 h. The solid was filtered, and washed with water. The solid was dried in a vacuum oven overnight to provide a white solid (0.15 g, 68%): ¹H NMR (300 MHz, DMSO-d₆) δ 8.33 (d, J=2.8 Hz, 1H), 7.64 (app q, J=6.7 Hz, 1H), 7.35 (dt, J=10.5, 2.5 Hz, 1H), 7.17 (dt, J=7.9, 1.8 Hz, 1H), 6.61 (s, 1H), 6.49 (d, J=2.8 Hz, 1H), 5.30 (s, 2H), 5.29 (s, 2H), 2.92 (q, J=4.6 Hz, 1H), 2.50 (s, 3H), 1.20-1.14 (m, 2H), 1.12-1.08 (m, 2H). ES-HRMS m/z 434.1090 (M+H calcd for C₂₁H₁₉ClF₂N₃O₃ requires 434.1078).

Example 780

3-Chloro-4-(2,4-difluorobenzyloxy)-1-[1-(2-hydroxy-2-methyl-propyl)-H-pyrazol-3-ylmethyl]-6-methyl-pyridin-2(1H)-one

Step 1. Preparation of the title compound. 3-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]pyrazole (0.24 mg, 0.65 mmol), 2N NaOH (1.5 mL, 3 mmol), benzyltriethylammonium chloride (0.1 g, 0.44 mmol), sodium iodide (10 mg), and 1-chloro-2-methyl propan-2-ol (0.07 mL, 0.71 mmol) were stirred in 5 mL of 1,4-dioxane at 85° C. for 19 h. The reaction was cooled to room temperature and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:9 MeOH/chloroform) provided a white solid (0.17 g, 58%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.65 (app q, J=8.5 Hz, 1H), 7.56 (d, J=2.2 Hz, 1H), 7.34 (dt, J=10.5, 2.5 Hz, 1H), 7.17 (dt, J=7.8, 1.7 Hz, 1H), 6.52 (s, 1H), 6.06 (d, J=2.2 Hz, 1H), 5.26 (s, 2H), 5.18 (s, 2H), 4.64 (s, 1H), 3.94 (s, 2H), 2.48 (s, 3H), 1.01 (s, 6H). ES-HRMS m/z 438.1378 (M+H calcd for C₂₁H₂₃ClF₂N₃O₃ requires 438.1390).

Example 781

5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-pyridin-1(2H)-ylmethyl]-1,3-dihydroisoindole-2-carboxylic Acid Tert-Butyl Ester

Step 1. Preparation of 2,3-dihydro-1H-isoindole-5-carboxylic Acid Methyl Ester Hydrochloride Salt

2-Benzyl-2,3-dihydro-1H-isoindole-5-carboxylic acid methyl ester (see, e.g., European patent EP 0343560A2) (3.0 g, 11.2 mmol), ammonium formate (1.4 g, 22.4 mmol) and palladium hydroxide (112 mg) were dissolved in 50 mL of methanol. The reaction was stirred at reflux for 15 h. The reaction was cooled to room temperature, the catalyst was filtered over Celite®, and the filtrate was evaporated on a rotary evaporator. The residue was dissolved in methanol, 1M HCl in Et₂O was added to provide a light yellow solid (1.6 g, 67%): ¹H NMR (300 MHz, DMSO-d₆) δ 9.80 (br s, 2H), 8.00 (s, 1H), 7.95 (d, J=8.0 Hz, 1H), 7.55 (d, J=7.9 Hz, 1H), 4.55 (d, J=4.1 Hz, 4H), 3.86 (s, 3H).

Step 2. Preparation of 1,3-dihydro-isoindole-2,5-dicarboxylic Acid 2-tert-butyl Ester 5-methyl Ester

2,3-Dihydro-1H-isoindole-5-carboxylic acid methyl ester hydrochloride salt (1.6 g, 7.5 mmol), triethylamine (2.1 mL, 15 mmol), DMAP (92 mg, 0.8 mmol) and Boc₂O (2.5 g, 11.3 mmol) were stirred in 15 mL of methylene chloride for 12 h. The reaction was diluted with methylene chloride, washed with 10% citric acid, brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:3 EtOAc/hexanes) gave a light yellow oil (1.34 g, 64%): ¹H NMR (300 MHz, CDCl₃) δ 7.97-7.90 (m, 2H), 7.35-7.27 (m, 1H), 4.72 (s, 2H), 4.68 (s, 2H), 3.92 (s, 3H), 1.52 (s, 9H).

Step 3. Preparation of 5-hydroxymethyl-1,3-dihydroisoindole-2-carboxylic Acid Tert-Butyl Ester

1,3-Dihydroisoindole-2,5-dicarboxylic acid 2-tert-butyl ester 5-methyl ester (1.3 g, 4.7 mmol) was dissolved in 15 mL of THF, cooled to −78° C., and DIBAL (15.2 mL of a 1M solution in toluene, 15.2 mmol) was added dropwise. The reaction was warmed room temperature and stirred for 12 h. The reaction was quenched with a 1:1 solution of 10% citric acid/methanol, and was evaporated on a rotary evaporator. The residue was dissolved in EtOAc, washed with (3 times) Rochelle salt, brine, dried (MgSO₄), and evaporated on a rotary evaporator. Trituration with EtOAc gave a white solid (0.35 g, 29%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.24 (s, 3H), 5.19 (s, 1H), 4.55 (s, 4H), 4.48 (d, J=5.7, 2H), 1.45 (s, 9H).

Step 4. Preparation of 5-bromomethyl-1,3-dihydroisoindole-2-carboxylic Acid Tert-Butyl Ester

5-Hydroxymethyl-1,3-dihydroisoindole-2-carboxylic acid tert-butyl ester (0.63 g, 2.5 mmol), triphenylphosphine (0.79 g, 3.0 mmol) and carbon tetrabromide (0.99 g, 3.0 mmol) were stirred in 10 mL of methylene chloride for 20 min. The reaction was evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:3 EtOAc/hexanes) gave a white solid (0.56 g, 72%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.44-7.24 (m, 3H), 4.71 (s, 2H), 4.57 (s, 2H), 4.55 (s, 2H), 1.45 (s, 9H).

Step 5. Preparation of the title compound. 5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-pyridin-1(2H)-ylmethyl]-1,3-dihydroisoindole-2-carboxylic acid tert-butyl ester was prepared by a procedure similar to the one described in Example 777 gave a yellow solid (1.4 g, 39%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.64 (app q, J=6.7 Hz, 1H), 7.39-7.27 (m, 2H), 7.17 (dt, J=8.5, 2.6 Hz, 1H), 7.08-7.03 (m, 2H), 6.59 (s, 1H), 5.29 (s, 4H), 4.55 (s, 2H), 4.53 (s, 2H), 2.32 (s, 3H), 1.44 (s, 9H). ES-HRMS m/z 517.1728 (M+H calcd for C₂₇H₂₈ClF₂N₂O₄ requires 438.1700).

Example 782

5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-pyridin-1(2H)-ylmethyl]-1-methyl-1,3-dihydroindol-2-one

Step 1. Preparation of the 3-chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(1-methyl-1H-indol-5-ylmethyl)-pyridin-2(1H)-one

3-Chloro-4-(2,4-difluoro-benzyloxy)-1-(1H-indol-5-ylmethyl)-6-methyl-pyridin-2(1H)-one (see Example 633) (1.2 g, 2.9 mmol) was dissolved in 12 mL of anhydrous DMF, cooled to 0° C., and NaH (0.14 g, 3.5 mmol) was added. The reaction was stirred at room temperature for 30 min., then dimethylsulfate (0.33 mL, 3.5 mmol), was added dropwise and the reaction was stirred at room temperature for 17.5 h. The reaction was diluted with water, and the precipitate was filtered off to afford a light, yellow solid (1.12 g, 90%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.66 (app q, J=9 Hz, 1H), 7.41-7.30 (m, 3H), 7.23-7.15 (m, 2H), 7.00 (d, J=8 Hz, 1H), 6.57 (s, 1H), 6.38 (s, 1H), 5.39 (s, 2H), 5.29 (s, 2H), 3.76 (s, 3H), 2.34 (s, 3H).

Step 2. Preparation of 3,3-dibromo-5-[3-chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-2H-pyridin-1-ylmethyl]-1-methyl-1,3-dihydroindol-2-one

3-Chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-1-(1-methyl-1H-indol-5-ylmethyl)-pyridin-2(1H)-one (1.12 g, 2.61 mmol) was diluted with 25 mL of t-BuOH, and pyridinium bromide perbromide (2.51 g, 7.83 mmol) was added portionwise over a period of 20 min. The reaction was stirred at room temperature for 16.5 h. The reaction was evaporated on a rotary evaporator, and the resulting solid dissolved in water, extracted with EtOAc, dried (Na₂SO₄), filtered, and concentrated under reduced pressure to give a dark, tan solid (1.4 g, 87%), which was carried forward without further purification or characterization.

Step 3. Preparation of the title compound. 3,3-Dibromo-5-[3-chloro-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-pyridin-1(H)-ylmethyl]-1-methyl-1,3-dihydro-indol-2-one (1.37 g, 2.27 mmol) and zinc dust (1.5 g, 23 mmol) were dissolved in 30 mL of acetic acid. The reaction was stirred at room temperature for 20 h. The reaction was diluted with water and extracted with EtOAc, washed with brine, dried (Na₂SO₄), filtered, and evaporated on a rotary evaporator to give a yellow solid (0.19 g, 19%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.63 (app q, J=8 Hz, 1H), 7.35 (app t, J=9 Hz, 1H), 7.21-7.08 (m, 2H), 7.03 (s, 1H), 6.93 (d, J=8 Hz, 1H), 6.57 (s, 1H), 5.28 (br s, 4H), 3.52 (s, 2H), 3.09 (s, 3H), 2.34 (s, 3H).

Example 783

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(2,3-dihydro-1H-isoindol-5-ylmethyl)-6-methyl-pyridin-2(1H)-one, Trifluoroacetic Acid Salt

Step 1. Preparation of the title compound. 5-[3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-2-oxo-pyridin-1(2H)-ylmethyl]-1,3-dihydroisoindole-2-carboxylic acid tert-butyl ester (0.14 mg, 0.27 mmol) was stirred in 10 mL of 9:1 dioxane/H₂SO₄ for 48 h. The reaction was evaporated on a rotary evaporator. Purification by preparatory HPLC (Phenomenex Luna 10μ, C18(2) 250×21.2 mm) provided a white solid (0.05 g, 34%): ¹H NMR (300 MHz, DMSO-d₆) δ 9.41 (br s, 2H), 7.66 (app q, J=6.7 Hz, 1H), 7.39-7.32 (m, 2H), 7.21-7.11 (m, 3H), 6.62 (s, 1H), 5.32 (s, 2H), 5.29 (s, 2H), 4.47 (s, 4H), 2.32 (s, 3H).

Example 784

5-[3-Chloro-4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]-1-methyl-1,3-dihydroindol-2-one

Step 1. Preparation of 3-chloro-4-(2,4-difluorobenzyloxy)-1-(1-methyl-1H-indol-5-ylmethyl)-pyridin-2(1H)-one

3-Chloro-4-(2,4-difluoro-benzyloxy)-1-(1H-indol-5-ylmethyl)-pyridin-2(1H)-one (0.26 g, 0.64 mmol), was dissolved with 4 mL of anhydrous DMF, cooled to 0° C., and NaH (0.031 g, 0.77 mmol) was added to the reaction. The reaction was stirred at 0° C. for 30 min., and then dimethyl sulfate (0.07 mL, 0.77 mmol) was added dropwise to the reaction. The reaction was allowed to warm to room temperature and stirred for 21 h. The reaction was diluted with water, and the precipitate was filtered and washed with water to afford an orange solid (0.230 g, 87%), which was carried forward without further purification or analysis.

Step 2. Preparation of 3,3-dibromo-5-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]-1-methyl-1,3-dihydroindol-2-one

3-Chloro-4-(2,4-difluorobenyloxy)-1-(1-methyl-1H-indol-5-ylmethyl)-pyridine-2(1H)-one (0.230 g, 0.554 mmol) was diluted with 5 mL of t-BuOH, and pryidinium bromide perbromide was added portionwise over a period of 15 min. The reaction was stirred at room temperature for 7 h. The reaction was evaporated on a rotary evaporator. The residue was diluted with water and extracted with EtOAc, dried over dried (Na₂SO₄), filtered, and evaporated on a rotary evaporator to provide an orange solid (0.329 g, 100%), which was carried forward without further purification or analysis.

Step 3. Preparation of title compound. 3,3-Dibromo-5-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]-1-methyl-1,3-dihydroindol-2-one (0.33 g, 0.55 mmol) and zinc dust (0.36 g, 5.5 mmol) were diluted with 10 mL of acetic acid. The reaction was stirred at room temperature for 15 h. The reaction was diluted with water and extracted with EtOAc, washed with brine, dried (Na₂SO₄), filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 100% EtOAc) provided an off-white solid (0.05 g, 21%). ¹H NMR (300 MHz, DMSO-d₆) δ 7.94 (d, J=8 Hz, 1H), 7.62 (app q, J=9 Hz, 1H), 7.37-7.28 (m, 2H), 7.24 (s, 1H), 7.15 (app t, J=9 Hz, 1H), 6.93 (d, J=8 Hz, 1H), 6.59 (d, J=8 Hz, 1H), 5.29 (s, 2H), 5.08 (s, 2H), 3.53 (s, 2H), 3.08 (s, 2H).

Example 785

3-Chloro-4-(2,4-difluorobenzyloxy)-1-[2-(2-hydroxy-2-methyl-propionyl)-2,3-dihydro-1H-isoindol-5-ylmethyl]-6-methyl-pyridin-2(1H)-one

Step 1. Preparation of title compound. 3-Chloro-4-(2,4-difluorobenzyloxy)-1-(2,3-dihydro-1H-isoindol-5-ylmethyl)-6-methyl-pyridin-2(1H)-one (0.061 g, 0.12 mmol), 1-chlorocarbonyl-1-methyethyl acetate (0.02 mL, 0.13 mmol), and NMM (0.03 mL, 0.23 mmol) were stirred in 3.0 mL of THF for 1.5 h. 2N Sodium hydroxide (0.300 mL) and MeOH (0.338 mL) were added to the reaction. The reaction continued to stir at room temperature for an additional 1 h. The reaction was evaporated on a rotary evaporator to afford an off-white solid (0.05 g, 82%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.66 (app q, J=8.6 Hz, 1H), 7.39-7.29 (m, 2H), 7.18 (app t, J=8.7 Hz, 1H), 7.11-7.02 (m, 2H), 6.60 (s, 1H), 5.33-5.29 (m, 4H), 5.08 (s, 2H), 4.64 (s, 2H), 2.33 (s, 3H), 1.33 (s, 6H).

Example 786

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(2,5-dimethyl-1,3-benzothiazol-6-yl)-6-methylpyridin-2(1H)-one

Step 1. Preparation of 2,5-dimethyl-6-nitro-1,3-benzothiazole

2,5-Dimethyl-1,3-benzothiazole (5.0 g, 31 mmol) and potassium nitrate (3.4 g, 34 mmol) were added, separately, in small portions to sulfuric acid at −5° C. and stirred for 19.5 h. The reaction was quenched with NH₄OH at 0° C., the solid was collected, and dried in a vacuum oven to provide a tan solid (2.5 g, 40%): ¹H NMR (300 MHz, DMSO-d₆) δ 8.84 (s, 1H), 7.99 (s, 1H), 2.63 (s, 3H), 2.42 (s, 3H).

Step 2. Preparation of 2,5-dimethyl-1,3-benzothiazol-6-ylamine

2,5-Dimethyl-6-nitro-1,3-benzothiazole (0.60 g, 2.9 mmol) and zinc dust (1.9 g, 29 mmol) were stirred in 30 mL of acetic acid at room temperature for 48 h. The reaction was diluted with water and extracted with EtOAc, washed with brine, dried (Na₂SO₄), filtered and evaporated on a rotary evaporator to give a tan solid (0.510 g, 99%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.46 (s, 1H), 7.05 (s, 1H), 5.05 (br s, 2H), 2.64 (s, 3H), 2.15 (s, 3H).

Step 3. Preparation of 1-(2,5-dimethyl-1,3-benzothiazol-6-yl)-4-hydroxy-6-methyl-pyridin-2(1H)-one

2,5-Dimethyl-1,3-benzothiazol-6-ylamine (0.51 g, 2.9 mmol), and 4-hydroxy-6-methyl-2-pyrone (0.36 g, 2.6 mmol) were diluted with 10 mL of trifluoroethanol, and the reaction was heated to 85° C. for 18.5 h. The reaction was cooled to room temperature, and evaporated on a rotary evaporator to give a brown solid (0.88 g, 100%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.75 (br s, 1H), 7.89 (s, 1H), 7.84 (s, 1H), 5.94 (d, J=1.5 Hz, 1H), 5.59 (d, J=2.4 Hz, 1H), 2.81 (s, 3H), 2.05 (s, 3H), 1.78 (s, 3H).

Step 4. Preparation of 3-chloro-1-(2,5-dimethyl-1,3benzothiazol-6-yl)-4-hydroxy-6-methyl-pyridin-2(1H)-one.

1-(2,5-Dimethyl-1,3-benzothiazol-6-yl)-4-hydroxy-6-methyl-pyridin-2(1H)-one (0.82 g, 2.9 mmol) and NCS (0.46 g, 3.4 mmol) were stirred in 10 mL of DMF for 50 h. The reaction was diluted with an 5% LiCl, extracted with EtOAc, washed with brine, dried (Na₂SO₄), filtered, and evaporated on a rotary evaporator that gave a brown semi-solid (0.23 g, 25%), which was carried forward without further purification or analysis.

Step 5. Preparation of title compound. 3-Chloro-1-(2,5-dimethyl-1,3-benzothiazol-6-yl)-4-hydroxy-6-methyl-pyridin-2(1H)-one (0.23 g, 0.71 mmol), cesium carbonate (0.46 g, 1.4 mmol) and 2,4-difluorobenzyl bromide (0.11 mL, 0.86 mmol), were diluted with 5 mL of anhydrous dioxane, and the reaction was heated at reflux for 21 h. The reaction was cooled to room temperature and diluted with EtOAc. The reaction was washed with water, brine, dried (Na₂SO₄), filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica gel, 100% EtOAc) to provide an orange solid (0.03 g, 8%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.95 (d, J=4.7 Hz, 2H), 7.71 (app q, J=8.6 Hz, 1H), 7.38 (app t, J=7.9 Hz, 1H), 7.21 (app t, J=8.5 Hz, 1H), 6.78 (s, 1H), 5.35(s, 2H), 2.83 (s, 3H), 2.06 (s, 3H), 1.92 (s, 3H).

Example 787

3-Chloro-4-(2,4-difluorobenzyloxy)-6-methyl-1-(3-methyl-1H-pyrazol-4-yl)pyridin-2(1H)-one

Step 1. Preparation of 3-methyl-4-nitro-1H-pyrazole

3-Methylpyrazole (4.9 mL, 61 mmol) was dissolved in 30 mL of H₂SO₄ cooled to −5° C. KNO₃ (6.8 g, 67 mmol) was added to the reaction portion-wise. The reaction was warmed to room temperature and stirred for 16 h. The reaction was neutralized with concentrated NH₄OH at 0° C., the solid was collected, and dried in a vacuum oven to provide a white solid (4.93 g, 64%): ¹H NMR (300 MHz, DMSO-d₆) δ 13.55 (br s, 1H), 8.39 (s, 1H), 2.50 (s, 3H).

Step 2. Preparation of 3-methyl-4-nitro-pyrazole-1-carboxylic Acid Tert-Butyl Ester

3-Methyl-4-nitro-1H-pyrazole (4.9 g, 39 mmol), triethylamine (6.0 mL, 43 mmol), DMAP (0.48 g, 3.9 mmol) and Boc₂O (17.8 g, 82 mmol) were stirred in 65 mL of acetonitrile for 20 h. The reaction was evaporated on a rotary evaporator. The residue was dissolved in EtOAc, washed with 10% citric acid, brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:1 EtOAc/hexanes) gave a yellow oil (8.8 g, 100%): ¹H NMR (300 MHz, DMSO-d₆) δ 9.19 (s, 1H), 2.48 (s, 3H), 1.47 (s, 9H).

Step 3. Preparation of 4-amino-3-methyl-pyrazole-1-carboxylic Acid Tert-Butyl Ester

3-Methyl-4-nitro-pyrazole-1-carboxylic acid tert-butyl ester (4.4 g, 19.4 mmol), and 10% palladium on carbon (250 mg) were suspended in 150 mL of methanol and subject to 20 psi of hydrogen on a Parr shaker for 24 h. The catalyst was removed over celite, and the filtrate was evaporated on a rotary evaporator. Purification by flash column chromatography (silica, EtOAc) gave a yellow oil (1.6 g, 42%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.25 (s, 1H), 4.28 (s, 2H), 2.07 (s, 3H), 1.51 (s, 9H).

Step 4. Preparation of 4-hydroxy-6-methyl-1-(3-methyl-1H-pyrazol-4-yl)-pyridin-2(1H)-one

4-Amino-3-methyl-pyrazole-1-carboxylic acid tert-butyl ester (2.0 g, 10 mmol) and 4-hydroxy-6-methyl-2-pyrone (1.3 g, 10 mmol) were diluted with 30 mL of trifluoroethanol, and the reaction was heated to 85° C. for 24 h. The reaction was cooled to room temperature, and evaporated on a rotary evaporator to give a brown solid (3.1 g, 100%), which was used without further purification or analysis.

Step 5. Preparation of 4-(2-4-difluorobenzyloxy)-6-methyl-1-(3-methyl-1H-pyrazol-4-yl)-pyridin-2(1H)-one

4-Hydroxy-6-methyl-1-(3-methyl-1H-pyrazol-4-yl)-pyridin-2(1H)-one (3.1 g, 10 mmol), cesium carbonate (6.6 g, 20 mmol) and 2,4-difluorobenzyl bromide (1.6 mL, 12 mmol), were diluted with 50 mL of anhydrous 1,4-dioxane, and the reaction was heated at reflux for 22 h. The reaction was cooled to room temperature and diluted with water. The reaction was extracted 3 times with EtOAc, washed with brine, dried (Na₂SO₄), filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica gel, 1:9 MeOH/chloroform) to provide an off-white solid (0.47 g, 14%): ¹H NMR (300 MHz, DMSO-d₆) δ 12.72 (br s, 1H), 8.32 (s, 1H), 7.63 (app q, J=8.6 Hz, 1H), 7.34 (dt, J=10.4, 2.5 Hz, 1H), 7.16 (dt, J=8.5, 1.8 Hz, 1H), 6.01 (d, J=2.0 Hz, 1H), 5.90 (d, J=2.6 Hz, 1H), 5.09 (s, 2H), 1.95 (s, 3H), 1.90 (s, 3H).

Step 6. Preparation of the title compound. 4-(2-4-Difluorobenzyloxy)-6-methyl-1-(3-methyl-1H-pyrazol-4-yl)-pyridin-2(1H)-one (0.46 mg, 1.4 mmol) and NCS (0.20 g, 1.5 mmol) were diluted with 5 m]L of DMF, and stirred for 14 h. The reaction was diluted with water, and extracted 3 times with EtOAc. The combined organics were washed with brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator. Purification (silica, 1:9 MeOH/chloroform) provided an off-white solid (0.10 g, 18%): 1H NMR (300 MHz, DMSO-d₆) δ 8.17 (br s, 1H), 7.57 (app q, J=6.4 Hz, 1H), 7.30 (s, 1H), 6.97 (dt, J=10.4, 2.0 Hz, 1H), 6.88 (dt, J=10.3, 2.4 Hz, 1H), 6.16 (s, 1H), 5.26 (s, 2H), 2.04 (s, 3H), 2.01 (s, 3H).

Example 788

3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylic Acid

Step 1 Preparation Diethyl 1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-3,5-dicarboxylate

Trifluoro acetic acid (5.4 mL, 70 mmol) and dihydropyran (7.2 mL, 77.7 mmol) were added sequentially to a room temperature solution of diethyl-3,5-pyrazole dicarboxylate (15 g, 70.7 mmol) in methylene chloride. After three hours, the reaction mixture was poured into saturated aqueous NaHCO₃ and extracted with additional methylene chloride. The organic extract was washed with brine, dried over anhydrous Na₂SO₄, decanted and concentrated in vacuo to give diethyl 1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-3,5-dicarboxylate as a white solid. ¹H NMR (400 MHz, CDCl₃) δ 7.35 (s, 1H), 6.31 (dd, J=2.76 and 10 Hz, 1H), 4.37 (q, J=7.2 Hz, 4H), 4.03 (m, 1H), 3.71 (dt, J=3.2 Hz, 1H), 2.53 (m, 1H), 2.1 (m, 1H), 1.97 (m, 1H), 1.71 (m, 2H), 1.57 (m, 1H), 1.37 (t, J=7.2 Hz, 6H).

Step 2. Preparation of Ethyl 3-(hydroxymethyl)-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate

Diisobutyl aluminum hydride (110 mL, 110 mmol, 1.0M solution in hexanes) was added dropwise to a −78 C solution of 1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-3,5-dicarboxylate (14.7 g, 49.6 mmol) in THF (100 mL). The reaction mixture was stirred at −78 C for 1 h., was warmed to 0° C. and was quenched by the drop wise addition of 30 mL of H₂O. This mixture was poured into saturated aqueous sodium potassium tartrate (300 mL) and was stirred for 30 min. at room temperature. Ethyl acetate was added, the layers were separated and the organic layer was washed with additional saturated sodium potassium tartrate solution. The ethyl acetate extract was dried with anhydrous Na₂SO₄, decanted and concentrated in vacuo to give the title product, ethyl 3-(hydroxymethyl)-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate, as a white solid. (11 g, 87%) ¹H NMR (400 MHz, CDCl₃) δ 6.88 (s, 1H), 6.26 (dd, J=2.4 and 10.4 Hz, 1H), 4.69 (s, 2H), 4.33 (q, J=8.4 Hz, 2H), 4.08 (m, 1H), 3.71 (t, J=9.6 Hz, 1H), 2.40 (m, 1H), 2.05 (m, 1H), 1.91 (m, 1H), 1.71 (m, 2H), 1.55 (m, 1H), 1.35 (t, J=8 Hz, 3H). ES-HRMS m/z 255.1323 (M+H calcd for C₁₂H₁₉N₂O₄ requires 255.1339.)

Step 3 Preparation of Ethyl 3-{[(methylsulfonyl)oxy]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate

A solution of ethyl 3-(hydroxymethyl)-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate (6 g, 23.6 mmol), and triethylamine (4 mL, 28.3 mmol) in methylene chloride (100 mL) was cooled to 0° C. Methane sulfonyl chloride (2 mL, 25.9 mmol) was added and the reaction mixture was stirred at 0° C. for 2 h. The solution was poured into saturated aqueous NaHCO₃ and extracted additional methylene chloride. The organic extract was washed with brine, dried with anhydrous Na₂SO₄, decanted and concentrated in vacuo to give ethyl 3-{[(methylsulfonyl)oxy]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate as a colorless oil which was used without further purification. (7.4 g, 95%) ¹H NMR (400 MHz, CDCl₃) δ 6.99 (s, 1H), 6.27 (dd, J=2.2 and 10 Hz, 1H), 5.26 (d, J=2.6 Hz, 2H), 4.33 (q, J=7.6 Hz, 2H), 4.06 (d, J=12 Hz, 1H), 3.71 (t, J=12 Hz, 1H), 2.98 (s, 3H), 2.37 (m, 1H), 2.06 (m, 1H), 1.91 (m, 1H), 1.70 (m, 2H), 1.56 (m, 1H), 1.36 (t, J=6.8 Hz, 3H). LC/MS, t_r=5.05 min. (5 to 95% acetonitrile/water over 8 min. at 1 ml/min with detection 254 nm, at 50° C.).

Step 4 Preparation of Ethyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate

Sodium hydride (0.73 g, 30.6 mmol) was added to a 0° C. suspension of the compound from Example 734 (5 g, 15.3 mmol) in tetrahydrofuran (100 mL). After 5 minutes, a solution of ethyl 3-{[(methylsulfonyl)oxy]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate (7.4 g, 23 mmol) in tetrahydrofuran (20 mL) was added and the reaction mixture was refluxed for 2 h. The solution was cooled to room temperature, poured into saturated aqueous NaHCO₃ and extracted with ethyl acetate. The organic extract was washed with brine, dried with anhydrous Na₂SO₄, decanted and concentrated in vacuo. The semi-solid residue was treated with acetonitrile and filtered. The filtrate was concentrated and treated with diethyl ether/hexanes and the title product, ethyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate, was isolated by filtration as a tan solid. (4.4 g, 51%) ¹H NMR (400 MHz, CDCl₃) δ 7.54 (td, J=6.5 and 8.5 Hz, 1H), 7.00 (s, 1H), 6.92 (m, 1H), 6.83 (dddd, J=2.6, 2.6, 8.9 Hz, 1H), 6.23 (dd, J=2.5 and 10.5 Hz, 1H), 5.93 (s, 1H), 5.27 (dd, 1H), 5.17 (s, 2H), 4.28 (q, J=6.5 Hz, 2H), 4.05 (m, 1H), 3.71 (td, J=2.5 Hz, 1H), 2.53 (s, 3H), 2.34 (m, 1H), 2.04 (m, 1H), 1.87 (d, 1H), 1.69 (t, 1H), 1.57 (m, 2H), 1.33 (t, J=7.3 Hz, 3H). ¹⁹F NMR (300 MHz, CD₃OD) δ −109.79 (1F), −115.06 (1 F). ES-HRMS m/z 566.1089 (M+H calcd for C₂₅H₂₇BrF₂N₃O₅ requires 566.1097).

Step 5 Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylic Acid

Sodium hydroxide (0.57 mL, 1.44 mmol, 2.5 M) was added to a solution of ethyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylate (0.68 g, 1.2 mmol) in tetrahydrofuran (10 mL), ethanol, and water (2 mL). After stirring at room temperature for 1 h., the reaction mixture was poured into saturated aqueous ammonium chloride, which was extracted with ethyl acetate. The organic extract was concentrated in vacuo to give a cloudy solution, which was treated with diethyl ether. The white powder was filtered and washed with additional ether to give 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylic acid, which was used without further purification. (0.7 g) ¹H NMR (400 MHz, dmso-d₆) δ 7.62 (q, J=8.4 Hz, 1H), 7.30 (m, 1H), 7.13 (td, J=2.3 and 8.8 Hz, 1H), 6.61 (dd, J=2.4 and 10.4 Hz, 1H), 6.49 (s, 1H), 6.14 (s, 1H), 5.25 (s, 2H), 5.12 (s, 2H), 4.0 (q, J=7.2 Hz, 2H), 3.84 (d, 1H), 3.46 (m, 1H), 3.33 (m, 1H), 2.15 (m, 1H), 1.96 (s, 3H), 1.90 (m, 1H), 1.66 (m, 1H), 1.45 (m, 1H), 1.14 (m, 1H). ¹⁹F NMR (300 MHz, dmso-d₆) δ −109.76 (1F), −113.72 (1 F). ES-HRMS m/z 538.0786 (M+H calcd for C₂₃H₂₃BrF₂N₃O₅ requires 538.0784).

Example 789

3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-1H-pyrazole-5-carboxamide

Step 1 Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-1H-pyrazole-5-carboxamide

A nitrogen flushed flask containing a solution of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylic acid (0.6 g, 1.1 mmol) in N,N-dimethyl formamide (30 mL) was cooled to 0° C. Triethylamine (0.12 mL, 1.1 mmol) and isobutyl chloroformate (0.14 mL, 1.1 mmol) were added and the reation mixture was stirred as it warmed to room temperature overnight. The reaction mixture was partitioned between ethyl acetate and saturated aqueous NaHCO₃. The organic extract was washed with brine and was concentrated in vacuo to give a white solid that was dissolved in tetrahydrofuran (15 mL), methanol (5 mL), water (5 mL) and concentrated HCl (1 mL). After stirring at room temperature for 2 h., the reaction mixture was brought to pH 12 with 2.5 N NaOH. The solution was partitioned between ethyl acetate and brine and the organic layer was concentrated in vacuo. The white solid was triturated with diethyl ether and filtered to give the desired product (0.23 g, 85%). ¹H NMR (400 MHz, CD₃OD) δ 7.59 (q, J=8.4 Hz, 1H), 7.01 (m, 2H), 6.59 (s, 1H), 6.47 (s, 1H), 5.36 (s, 2H), 5.27 (s, 2H), 2.84 (s, 3H), 2.50 (s, 3H). ¹⁹F NMR (300 MHz, CD₃OD) δ −111.64 (1F), −116.07 (1 F). ES-HRMS m/z 467.0558 (M+H calcd for C₁₉H₁₈BrF₂N₄O₃ requires 467.0525).

Example 790

3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1H-pyrazole-5-carboxamide

Step 1 Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1H-pyrazole-5-carboxamide

N-methyl morpholine (0.6 mL, 5.4 mmol) was added to a suspension of the compound from Example 788 (1 g, 1.8 mmol) in tetrahydrofuran (30 mL). When the solution became clear, 2-chloro-4,6-dimethoxy-1,3,5-triazine (0.4 g, 2.2 mmol) was added. After the reaction mixture was stirred at room temperature for 2 h., concentrated ammonium hydroxide (14 mL) was added. The mixture was stirred at room temperature for an additional h. and was then diluted with water and filtered. The white solid was suspended in a mixture of tetrahydrofuran (20 mL), methanol (15 mL), water (5 mL) and concentrated HCl (2 mL). After stirring at room temperature for 1 h., the solution was brought to pH 12 with 2.5 N NaOH. The solution was extracted with ethyl acetate and the organic extract was concentrated in vacuo. The resulting solid was triturated with diethyl ether to give the title compound as a white powder (0.5 g). ¹H NMR (400 MHz, dmso-d₆) δ 7.93 (s, 1H), 7.62 (q, J=8 Hz, 1H), 7.30 (m, 2H), 7.14 (t, J=9.6 Hz, 1H), 6.57 (s, 1H), 6.50 (s, 1H), 5.24 (s, 2H), 5.19 (s, 2H), 1.59 (s, 3H). ¹⁹F NMR (300 MHz, dmso-d₆) δ −109.71 (1F), −113.71 (1 F). ES-HRMS m/z 453.0385 (M+H calcd for C₁₈H₁₆BrF₂N₄O₃ requires 453.0368).

Example 791

3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethyl-1H-pyrazole-5-carboxamide

Step 1 Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethyl-1H-pyrazole-5-carboxamide

To a solution of the compound from Example 788 (0.35 g, 0.65 mmol) in N,N′-dimethylformamide (20 mL) was added N-methyl morpholine (0.1 mL, 0.97 mmol) and isobutyl chloroformate (0.13 mL, 0.97 mmol). After stirring the mixture at room temperature for 15 min., N,N′-dimethyl amine (0.65 mL, 1.3 mmol, 2.0M in THF) was added. When the reaction was complete, the solution was partitioned between saturated aqueous NaHCO₃ and ethyl acetate. The organic extract was washed with brine, dried with anhydrous Na₂SO₄, decanted and concentrated. The resulting oil was dissolved in a mixture of tetrahydrofuran (20 mL), methanol (10 mL), water (2 mL) and concentrated HCl (1 mL). After stirring at room temperature for 1 h., the reaction mixture was poured into saturated aqueous NaHCO₃ and was extracted with ethyl acetate. The organic extract was washed with brine, dried with anhydrous Na₂SO₄ and concentrated in vacuo. The resulting solid was triturated with diethyl ether and the title compound was isolated as a white powder (0.217 g, 69%). ¹H NMR (400 MHz, CD₃OD) δ 7.59 (q, J=7.6 Hz, 1H), 7.01 (m, 2H), 6.53 (s, 1H), 6.47 (s, 1H), 5.37 (s, 2H), 5.27 (s, 2H), 3.23 (s, 3H), 3.06 (s, 3H), 2.52 (s, 3H). 9 F NMR (300 MHz, CD₃OD) δ −111.72 (1F), −116.07 (1 F). ES-HRMS m/z 481.0687 (M+H calcd for C₂₀H₂₀BrF₂N₄O₃ requires 481.0673).

Example 792

3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-methoxyethyl)-1H-pyrazole-5-carboxamide

Step 1. Preparation of 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-methoxyethyl)-1H-pyrazole-5-carboxamide To a solution of the compound from Example 788 (0.35 g, 0.65 mmol) in N,N′-dimethylformamide (20 mL) was added N-methyl morpholine (0.1 mL, 0.97 mmol) and isobutyl chloroformate (0.13 mL, 0.97 mmol). After stirring the mixture at room temperature for 15 min., 2-methoxy ethylamine (0.11 mL, 1.3 mmol) was added. When the reaction was complete, the solution was partitioned between saturated aqueous NaHCO₃ and ethyl acetate. The organic extract was washed with brine, dried with anhydrous Na₂SO₄, decanted and concentrated. The resulting oil was dissolved in a mixture of tetrahydrofuran (20 mL), methanol (10 mL), water (2 mL) and concentrated HCl (1 mL). After stirring at room temperature for 1 h., the reaction mixture was poured into saturated aqueous NaHCO₃ and was extracted with ethyl acetate. The organic extract was washed with brine, dried with anhydrous Na₂SO₄ and concentrated in vacuo. The resulting solid was triturated with diethyl ether and the product was isolated as a white powder (43 mg, 13%). ¹H NMR (400 MHz, CD₃OD) δ 7.60 (q, J=7.6 Hz, 1H), 7.01 (m, 2H), 6.62 (s, 1H), 6.47 (s, 1H), 5.37 (s, 2H), 5.27 (s, 2H), 3.49 (m, 4H), 3.33 (s, 3H), 2.49 (s, 3H). ¹⁹F NMR (300 MHz, CD₃OD) δ −111.69 (1F), −116.08 (1 F). ES-HRMS m/z 511.0793 (M+H calcd for C₂₁H₂₂BrF₂N₄O₄ requires 511.0793).

The following table of non-limiting compounds can be made from the compound of Example 788 by coupling with the appropriate amine and cleavage of the tetrahydropyranyl protecting group.

Example R
788-A   CONH(CH2)nOH
788-B   CONHCH2C(Me)2OH
788-C   CONH(CH2)nNH2
788-D   CONH(CH2)nNHCH3
788-E   CONH(CH2)nN(CH3)2
788-F   CONHCH2CH(OH)CH2OH

The following table of compounds can be made from the compound of Example 790 by reduction of the amide and coupling acids including amino acids to the resulting amine residue. Non-limiting compounds are:

Example R
790-A   CH2NHCOCH2NH2
790-B   CH2NHCOCH2OH
790-C   CH2NHCOCH(NH2)CH2OH

Example 793

3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[1-(methylsulfonyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound of Example 88 (200 mg, 0.5 mmol), methanesulfonyl chloride (41 μL, 0.52 mmol), triethylamine (134 μL, 1.1 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 20 min. the reaction was completed by LC-MS. The compound precipitated out of solution. The precipitated was filtered and washed with water and diethyl ether to obtain the title compound (200 mg, 84%) as a solid. ¹H NMR (400 MHz, (d₆-DMSO) δ 7.7 (q, J=8.6 and 6.7 Hz, 1H), 7.3 (t, J=9.5 Hz, 1H), 7.3 (m, 2H), 7.0 (m, 2H), 6.6 (s, 1H), 5.3 (s, 2H), 3.9 (t, J=8.3 Hz, 2H), 2.9(m, 2H), 2.8 (s, 3H), 2.3 (s, 3H), 1.0 (t, J=7.25 Hz, 2H) ppm. ES-HRMS m/z 495.0970 (M+H calcd for C₂₃H₂₂ClF₂N₂O₄S requires 495.0951).

Example 794

2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-2-oxoethyl Acetate

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound from Example 88 (200 mg, 0.5 mmol), acetoxyacetyl chloride (59 μL, 0.55 mmol), triethylamine (140 μL, 1.0 mmol) and tetrahydrofuran (3.0 mL). After stirring at 25° C. for 20 min. the reaction was completed as determined by LC-MS. The compound precipitated out of solution. The precipitated solid was filtered and washed with water and diethyl ether to obtain the title compound (180 mg, 72%) as a white solid. ¹H NMR (400 MHz, (d₆-DMSO) δ 7.9 (d, J=8.3, 1H), 7.6 (q, J=7.5 and 8.0 Hz, 1H), 7.3 (t, J=9.7 Hz, 1H), 7.1 (t, J=8.3 Hz, 1H), 6.8 (m, 2H), 6.5 (s, 1H), 5.2 (s, 2H), 4.7 (s, 2H), 3.9 (t, J=7.9 Hz, 2H), 3.5(s, 2H), 3.0 (t, J=7.8 Hz, 2H), 2.3 (s, 3H), 1.9 (s, 3H) ppm. ES-HRMS m/z 517.1343 (M+H calcd for C₂₆H₂₄ClF₂N₂O₅ requires 517.1336).

Example 795

2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-1,1-dimethyl-2-oxoethyl Acetate

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound from Example 88 (200 mg, 0.5 mmol), 1-chlorocarbonyl-1-methylethyl acetate (80 μL, 0.55 mmol), triethylamine (140 μL, 1.0 mmol) and tetrahydrofuran (3.0 mL). After stirring at 25° C. for 20 min., the reaction was completed as determined by LC-MS. The compound precipitated out of solution. The precipitated solid was filtered and washed with water and diethyl ether to obtain the title compound (180 mg, 72%) as a white solid. ¹H NMR (400 MHz, (d₆-DMSO) δ 7.9 (d, J=8.3, 1H), 7.6 (d, J=6.4 Hz, 1H), 7.3 (t, J=9.8 Hz, 1H), 7.1 (s, 1H), 6.9 (m, 2H), 6.5 (s, 1H), 5.1 (s, 4H), 3.9 (s, 2H), 2.9 (s, 2H), 2.3 (s, 3H), 2.0 (s, 3H), 1.5 (s, 6H) ppm. ES-HRMS n2/z 545.1632 (M+H calcd for C₂₈H₂₈ClF₂N₂O₅ requires 545.1649).

Example 796

N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzyl}acetamide

Step 1: Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzamide

A 25 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the acid (Example 725, step 1) (785 mg, 1.7 mmol), 4-methylmorpholine (0.55 mL, 5 mmol), 2-chloro-4,6-dimethoxy-1,3,5-triazine (353 mg, 2 mmol) and tetrahydrofuran (9 mL). After stirring the mixture for 30 min. at 25° C., NH₄OH (4 mL) was added. The mixture was stiffed for 12 h. and diluted with water. The product precipitated from solution. The precipitated solid was filtered and washed with water and diethyl ether to give the title compound (624 mg, 78%) as a white solid. ¹H NMR (400 MHz, (d₆-DMSO) δ 7.8 (t, J=11.8 Hz, 2H), 7.65 (m, 2H), 7.56 (t, J=7.9 Hz, 1H), 7.35 (td, J=2.5 and 9.3 Hz, 1H) 7.17 (q, J=8.5 and 2.6 Hz, 1H), 5.4 (s, 2H), 2 (s, 3H) ppm. ES-HRMS m/z 467.0215 (M+H calcd for C₂₀H₁₅BrF₃N₂O₃ requires 467.0213).

Step 2: Preparation of 1-[4-(aminomethyl)-2-fluorophenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Hydrochloride

A 100 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound from Example 725, Step 1(2.31 g, 4.9 mmol), BH₃.DMS complex (0.7 mL, 7.4 mmol), and dichloromethane (49 mL). The mixture was refluxed for 24 h., allowed to cool to room temperature and quenched with HCl (6N). The organics were evaporated and the remaining aqueous solution was saturated with NaOH (2.5N) and extracted with dichloromethane. The organic phase was dried with Na₂SO₄ and concentrated in vacuo. HCl (6N) was added, concentrated in vacuo, and recrystallized from acetonitrille to furnish the title compound (1.5 g, 70%) as a white solid. ¹H NMR (400 MHz, (d₆-DMSO) δ 7.6 (q, J=8.5 and 6.8 Hz 1H), 7.5 (d, 11 Hz, 1H), 7.4 (t, J=7.9 Hz, 1H), 7.3 (d, J=7.9 Hz, 1H), 7.2 (t, J=10 Hz, 1H), 7.0 (t, J=8.6 Hz 1H), 6.7 (s, 1H) 5.36 (s, 2H), 4.1 (d, J=5.4 Hz, 2H), 2 (s, 3H) ppm. ES-HRMS m/z 453.0398 (M+H calcd for C₂₀H₁₇BrF₃N₂O₂ requires 453.0420).

Step 3: Preparation of N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzyl}acetamide

A 10 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound from Step 2 (above) (180 mg, 0.37 mmol), acetyl chloride (26 μL, 0.37 mmol), triethylamine (103 μL, 1.7 mmol) and tetrahydrofuran (4.0 mL). After stirring at 25° C. for 15 min. the reaction was completed as determined by LC-MS. The reaction mixture was poured into a saturated aqueous NH₄Cl solution. The aqueous mixture was extracted with ethyl acetate. The organic phase was dried with Na₂SO₄ and concentrated in vacuo to obtain the title compound (110 mg, 60%) as a solid. ¹H NMR (400 MHz, CD₃OD) δ 7.6 (s, 1H), 7.5-6.9 (m, 6H), 6.6 (s, 1H), 5.2 (s, 2H), 4.2 (s, 2H), 2.1-1.7 (m, 6H) ppm. ES-HRMS m/z 495.0541 (M+H calcd for C₂₂H₁₉BrF₃N₂O₃ requires 495.0526).

Example 797

5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-2-vinylbenzamide

Step 1: Preparation of methyl 2-bromo-5-methylbenzoate

Acetyl chloride (16.5 mL, 232.6 mmol) was added to a 0 C solution of 2-bromo-5-methyl benzoic acid (25 g, 116.3 mmol) in methanol (200 mL). After the reaction mixture was warmed to room temperature, the solution was refluxed for 2 h. The reaction mixture was cooled to room temperature and was concentrated to ¼ the original volume. The residue was diluted with ethyl acetate and saturated aqueous NaHCO₃. After extracting with ethyl acetate, the organic extract was washed with brine, dried with MgSO₄ and concentrated in vacuo to give methyl 2-bromo-5-methylbenzoate which was used without further purification. ¹H NMR (400 MHz, CD₃OD) δ 7.54 (m, 2H), 7.21 (m, 1H), 3.88 (s, 3H), 2.32 (s, 3H). LC/MS, t_r=5.97 min. (5 to 95% acetonitrile/water over 8 min. at 1 ml/min with detection 254 nm, at 50° C.).

Step 2: Preparation of Methyl 2-bromo-5-(bromomethyl)benzoate

A mixture of solid N-bromo succinimide (4.3 g, 24 mmol) and benzoylperoxide (0.5 g, 2.1 mmol) was added to a 75° C. solution of the product of Step 1(5 g, 21.8 mmol) in carbon tetrachloride (50 mL). After the reaction mixture was refluxed for 2 h., it was cooled to room temperature and the solution was filtered. The filtrate was concentrated in vacuo and the product, methyl 2-bromo-5-(bromomethyl)benzoate, was used without further purification. ¹H NMR (400 MHz, CDCl₃) δ 7.60 (m, 3H), 4.42 (s, 2H), 3.93 (s, 3H). LC/MS, t_r=5.73 min. (5 to 95% acetonitrile/water over 8 min. at 1 m/min with detection 254 nm, at 50° C.).

Step 3: Preparation of Methyl 2-bromo-5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoate

Sodium hydride (0.22 g, 9.2 mmol, 60% in mineral oil) was added to a 0 C slurry of the compound from Example 734 (1.5 g, 4.6 mmol) in 1,4-dioxane (40 mL). A solution of the product of Step 2 (2.2 g, 7 mmol) in 1,4-dioxane (10 mL) was added and the reaction mixture was heated to 100° C. for 18 h. The solution was cooled to room temperature, poured into water and extracted with ethyl acetate. The organic extract was washed with brine and concentrated in vacuo. The resulting solid was triturated with acetonitrile and diethyl ether to give the title compound as a tan solid (1.2 g, 48%). ¹H NMR (400 MHz, CDCl₃) δ 7.57 (m, 3H), 7.15 (dd, J=2.2 and 8 Hz, 1H), 6.95 (m, 1H), 6.85 (m, 1H), 6.00 (s, 1H), 5.31 (s, 2H), 5.20 (s, 2H), 3.91 (s, 3H), 2.29 (s, 3H). ¹⁹F NMR (400 MHz, CDCl₃) δ −109.53 (1F), −114.97 (1F). LC/MS, t_r=6.01 min. (5 to 95% acetonitrile/water over 8 min. at 1 ml/min with detection 254 nm, at 50° C.).

Step 4: Preparation of Methyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-vinylbenzoate

A 50 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound from Step 3 (4.3 g, 7.7 mmol), ethylene glycol dimethyl ether (62 mL) and Pd(PPh₃)₄ (5 mg, cat.). The mixture was stirred for 20 min at room temperature. Potassium carbonate (1.1 g, 7.7 mmol), water (19 mL) and trivinylcyclotriboroxane-pyridine complex (1.8 g, 7.7 mmol) were added and the mixture was refluxed. After 4 h. the reaction was completed as determined by LC-MS. The reaction was cooled to room temperature and extracted with ethyl acetate and dried over sodium sulfate. The crude was evaporated to dryness, the residue suspended with methanol and filtered to give the product as a white solid (2.1 g, 71%). ¹H NMR (400 MHz, CDCl₃) δ 7.7 (s, 1H), 7.6 (m, 1H), 7.5 (d, J=8.1 Hz, 1H), 7.4 (m, 1H), 7.3 (m, 1H), 7.0 (t, J=8.4 Hz, 1H), 6.8 (t, J=8.1 Hz, 1H), 6.0 (s, 1H), 5.6 (d, J=17 Hz, 1H), 5.3 (m, 3H), 5.2 (s, 2H), 3.8 (s, 3H), 2.4 (s, 3H) ppm. ES-HRMS m/z 504.0588 (M+H calcd for C₂₂H₂₁BrF₂NO₄ requires 504.0617).

Step 5: Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-vinylbenzoic Acid

A 50 mL round bottomed flask equipped with stirbar was charged with the compound from Step 4 (1.3 g, 2.6 mmol), NaOH (2.5 mL, 5.2 mmol, 2.5N), tetrahydrofuran (13 mL), methanol (5 mL) and water (5 mL). The mixture was stirred for 1 h., acidified with HCl, extracted with ethylacetate and dried over sodium sulfate. The solution was concentrated and the product precipitated with methanol to give the title compound as a solid (640 mg, 51%). ¹H NMR (400 MHz, CDCl₃) δ 7.8 (s, 1H), 7.6-7.4 (m, 3H), 7.3 (d, J=7.9 Hz, 1H), 7.0 (t, J=8.3 Hz, 1H), 6.8 (t, J=8.2 Hz, 1H), 6.0 (s, 1H), 5.6 (d, J=17 Hz, 1H), 5.3 (m, 3H), 5.2 (s, 2H), 2.4 (s, 3H) ppm. ES-HRMS m/z 490.0479 (M+H calcd for C₂₃H₁₉BrF₂NO₄ requires 490.0460).

Step 6: Preparation of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-2-vinylbenzamide

A 50 mL round bottomed flask equipped with stirbar and nitrogen inlet was charged with the compound from Step 5 (640 mg, 1.3 mmol) in dimethylformamide (13 mL) was cooled to −10° C. Isobutylchloroformate (0.17 mL, 1.3 mmol) and 4-methylmorpholine (0.14 mL, 1.3 mmol) were added and stirred for 20 min. Methylamine (1.3 mL. 2.6 mmol, 2M in THF) was added and stirred for 12 h. The solvent was evaporated and the residue was suspended with methanol to give the title product (657 mg, 79%) as a solid. ¹H NMR (400 MHz, CDCl₃) δ 7.56 (q, J=8.5 and 6.5 Hz, 1H), 7.5 (d, J=8 Hz, 1H), 7.2 (m, 2H), 6.9 (m, 2H), 6.8 (t, J=7.9 Hz, 1H), 6.0 (s, 1H), 5.6 (d, J=17.5 Hz, 1H), 5.3 (d, J=11 Hz, 3H), 5.2 (s, 2H), 2.9 (s, 3H), 2.3 (s, 3H) ppm. ES-HRMS m/z 503.0780 (M+H calcd for C₂₄H₂₂BrF₂N₂O₃ requires 503.0776).

Example 798

5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-(1,2-dihydroxyethyl)-N-methylbenzamide

A 50 mL round bottomed flask equipped with stirbar was charged with the compound Example 797 (above) (500 mg, 0.99 mmol), N-methylmorpholine oxide (291 mg, 2.47 mmol), and osmium tetroxide (91 μL, 25% in water, cat.). The mixture was stirred for 12 h. and the volatiles were evaporated. The water residue was extracted with ethylacetate and the organic phase washed with water and dried over sodium sulfate. Half of the volume of the ethyl acetate was evaporated and the product precipitated upon standing and the solid was filtered to give the title compound (323 mg, 61%). ¹H NMR (400 MHz, d₆-DMSO) δ 8.2 (d, J=4 Hz, 1H), 7.6 (q, J=8.3 and 7.6 Hz, 1H), 7.4 (d, J=8.0 Hz, 1H), 7.25 (t, J=9.5 Hz, 1H), 7.13 (t, J=8.7 Hz, 1H), 7.09 (d, J=8.5 Hz, 1H), 7.05 (s, 1H), 6.5 (s, 1H), 5.2 (s, 2H), 4.75 (m, 2H), 3.4 (m, 2H), 2.7 (s, 3H), 2.3 (s, 3H) ppm. ES-HRMS m/z 537.0848 (M+H calcd for C₂₄H₂₄BrF₂N₂O₅ requires 537.0831).

Example 799

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-5-yl]methyl}pyridin-2(1H)-one

Step 1. Preparation of Methyl 2-(methylthio)pyrimidine-5-carboxylate

A solution of the sodium salt of 3,3-dimethoxy-2-methoxycarbonylpropen-1-ol (5.0 g, 25 mmol), 2-methyl-2-thiopseudourea sulfate (3.5 g, 25 mmol) in anhydrous methanol (25 mL) was refluxed for 3 h. under anhydrous conditions. The reaction mixture was cooled and diluted with ethyl acetate. The reaction mixture was filtered and the residue was washed with ethyl acetate. The filtrate was concentrated and the residue was purified by flash chromatography (silica gel) using 25% ethyl acetate in hexane to afford the desired product (3.5 g, 75%) as a white powder. ¹H-NMR (d₆-DMSO, 400 MHz) δ 9.0 (s, 2H), 3.92 (s, 3H), 2.58 (s, 3H); ES-HRMS m/z 185.041 (M+H calcd for C₇H₈N₂O₂S requires 185.0379).

Step 2. Preparation of [2-(methylthio)pyrimidin-5-yl]methanol

To a cold suspension of methyl 2-(methylthio)pyrimidine-5-carboxylate (from Step 1) (1.74 g, 9.4 mmol) in dichloromethane (20 mL, −70° C.) was added DIBAL (20.8 mL, 20 mmol) dropwise via an addition funnel. The mixture was stirred under nitrogen at −70° C. for 1 h. and then at −50° C. for 3 h. The reaction was diluted with dichloromethane (50 mL) and quenched with a suspension of sodium sulfate decahydrate (10 g) in water (50 mL). The slurry was filtered through Celite® and the filtrate was concentrated. The residue was purified by flash chromatography (silica gel) using 100% ethyl acetate to afford the desired compound (0.7813 g, 39%) as a yellow solid. ¹H-NMR (CD₃OD, 400 MHz) δ 8.53 (s, 2H), 4.56 (s, 2H), 2.54 (s, 3H); ES-HRMS m/z 157.0409 (M+H calcd for C₆H₉N₂OS requires 157.0430).

Step 3. Preparation of 5-(Chloromethyl)-2-(methylthio)pyrimidine

To a cold solution of [2-(methylthio)pyrimidin-5-yl]methanol (from Step 2) (0.7813 g, 5.0 mmol) in anhydrous dichloromethane (10 mL, 0° C.) was added triethylamine (0.836 mL, 8.2 mmol) followed by the addition of methanesulfonyl chloride (0.465 mL, 6.0 mmol). The reaction mixture stirred at 0° C. under a nitrogen atmosphere for 30 min. then at room temperature for 3.5 h. The reaction was quenched with sodium bicarbonate (5%, 100 mL)) and extracted with dichloromethane (50 mL). The organic extracts were concentrated and the residue was purified by flash chromatography (silica gel) using 15% ethyl acetate in hexane to afford the desired compound (0.720 g, 82%) as a white solid. ¹H-NMR ((CD₃OD, 400 MHz) δ 8.60 (s, 2H), 4.64 (s, 2H), 2.54 (s, 3H); ES-HRMS m/z 175.0106 (M+H calcd for C₆H₇N₂CIS requires 175.0091).

Step 4. Preparation of Title Compound 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-5-yl]methyl}pyridin-2(1H)-one

To a solution of 5—(Chloromethyl)-2-(methylthio)pyrimidine (from Step 3) (0.62 g, 3.56 mmol) in anhdrous DMF (10 mL) was added KBr (0.424, 3.56 mmol). After the suspension stirred at room temperature for 30 min., 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (1.05 g, 3.19 mmol) was added followed by NaH (0.102 g, 4.25 mmol). The reaction mixture stirred at 70° C. under a nitrogen atmosphere for 3.5 h. The solvent was distilled and the residue was washed with water and extracted with ethyl acetate. The organic extracts were concentrated and the residue was purified by reverse phase HPLC using a 10-90% acetonitrile/water (30 min. gradient) at a 70 ml/min flow rate to afford the desired TFA salt (0.32 g, 15%) as a white powder. The TFA compound was washed with sodium bicarbonate (5%) and extracted with dichloromethane. The organic extract was concentrated to afford the desired compound (0.295 g, 18%) as a yellow solid. ¹H-NMR (CD₃OD, 400 MHz) δ 8.47 (s, 2H), 7.62 (q, 1H, J=8 Hz), 7.03 (m, 2H), 6.51 (s, 1H), 5.31 (s, 2H), 5.29 (s, 2H), 2.52 (s, 3H), 2.47 (s, 3H); ES-HRMS m/z 468.0174 (M+H calcd for C₁₉H₁₇N₃O₂F₂BrS requires 468.0187.

Example 800

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-5-yl]methyl}pyridin-2(1H)-one

To a solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-5-yl]methyl}pyridin-2(1H)-one (0.26 g, 0.55 mmol) in acetonitrile: water (4:1 v/v, 10 mL) was added MMPP (0.549 g, 1.1 mmol). The reaction stirred at room temperature for 30 h. The reaction mixture was diluted with ethyl acetate and filtered. The filtrate was concentrated and the residue was purified by reverse phase HPLC using a 10-90% acetonitrile/water (30 min. gradient) at a 70 ml/min flow rate to afford the desired TFA salt (0.13 g, 38%) as a white powder. ¹H-NMR (CD₃OD, 400 MHz) δ 8.86 (s, 2H), 7.62 (q, 1H, J=8 Hz), 7.02 (m, 2H), 6.56 (s, 1H), 5.48 (s, 2H), 5.31 (s, 2H), 3.34 (s, 3H), 2.49 (s, 3H); ES-HRMS m/z 500.0109 (M+H calcd for C₁₉H₁₇N₃O₄F₂BrS requires 500.0086).

Example 801

1-[(2-aminopyrimidin-5-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

To a cold solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl) pyrimidin-5-yl]methyl}pyridin-2(1H)-one (Example 800) (0.50 g, 1 mmol) in methanol (30 mL) was bubbled in ammonia gas. The reaction mixture was stoppered and stirred at room temperature over weekend. Concentrated to remove methanol and purified residue by reverse phase HPLC using a 10-90% acetonitrile in water (30 min. gradient) at a 100 mL/min flow rate to isolate two compounds. Each were washed with NaHCO₃ and extracted with ethyl acetate. The organic extracts were dried over anhydrous Na₂SO₄ and concentrated to afford two products, one of which was the desired compound (0.040 g). ¹H-NMR (CD₃OD, 400 MHz) δ 8.26 (s, 2H), 7.60 (q, 1H, J=8 Hz), 7.01 (m, 2H), 6.48 (s, 1H), 5.27 (s, 2H), 5.19 (s, 2H), 2.48 (s, 3H); ES-HRMS m/z 437.0415 (M+H calcd for C₁₈H₁₆N₄O₂F₂Br requires 437.0419).

Example 802

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-methoxypyrimidin-5-yl)methyl]-6-methylpyridin-2(1H)-one

A second compound was isolated from the synthesis detailed in Example 801, above. ¹H-NMR (CD₃OD, 400 MHz) δ 8.5 (s, 2H), 7.60 (q, 1H, J=8 Hz), 7.01 (m, 2H), 6.50 (s, 1H), 5.31 (s, 2H), 5.28 (s, 2H), 3.97 (s, 3H), 2.48 (s, 3H); ES-HRMS m/z 452.0440 (M+H calcd for C₁₉H₁₇N₃O₃F₂Br requires 452.0416).

Example 803

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylamino)pyrimidin-5-yl]methyl}pyridin-2(1H)-one

To a solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-5-yl]methyl}pyridin-2(1H)-one (Example 800) (0.35 g, 0.7 mmol) in anhydrous THF (5 mL) was added methylamine (1.4 mL of 2M solution in THF). The reaction mixture was stoppered and stirred at room temperature over the 2-3 days. The reaction mixture became turbid upon stirring. The reaction mixture was diluted in water (15 mL) and chilled in an ice bath. The solid was filtered and washed with ethyl acetate to afford the desired product (0.1074 g, 34% yield) as a white solid. ¹H-NMR (CD₃OD, 400 MHz) δ 8.24 (s, 2H), 7.60 (q, 1H, J=8 Hz), 7.01 (m, 2H), 6.47 (s, 1H), 5.27 (s, 2H), 5.18 (s, 2H), 2.87 (s, 3H), 2.48 (s, 3H); ES-HRMS m/z 451.0575 (M+H calcd for C₁₉H₁₇N₄O₄F₂Br requires 451.0576).

Example 804

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(dimethylamino)pyrimidin-5-yl]methyl}-6-methylpyridin-2(1H)-one

To a solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-5-yl]methyl}pyridin-2(1H)-one (0.325 g, 0.65 mmol) in anhydrous THF (5 mL) was added N,N-dimethylamine (1.6 mL of 2M solution in THF). The reaction mixture was stoppered and stirred at room temperature over the weekend. Reaction mixture became turbid upon stirring. The reaction mixture was diluted in water (20 mL) and chilled in an ice bath. The white solid was purified by reverse phase HPLC 10-90% acetonitrile/water (30 min. gradient) at a 70 ml/min flow rate to afford the desired TFA salt (0.40 g, 11%). ¹H-NMR (CD₃OD, 400 MHz) δ 8.33 (s, 2H), 7.62 (q, 1H, J=8 Hz), 7.02 (m, 2H), 6.56 (s, 1H), 5.27 (s, 2H), 5.20 (s, 2H), 3.10 (s, 6H), 2.49 (s, 3H); ES-HRMS m/z 465.0732 (M+H calcd for C₂₀H₂₀N₄O₄F₂Br requires 465.0732).

Example 805

5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile

To a suspension of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-5-yl]methyl}pyridin-2(1H)-one (Example 800) (1.355 g, 0.27 mmol) in anhydrous DMF (10 mL) was added sodium cyanide (0.132 g, 0.27 mmol). Shortly after beginning the stirring of the suspension at room temperature, the reaction mixture became dark orange. The mixture was stirred at room temperature for 1 h. The solvent was distilled and the residue was washed with a water/acetonitrile (1:1 v/v, 30 mL). The residue was chilled and filtered to afford the desired product as an orange solid (0.942 g, 91% yield). ¹H-NMR (CD₃OD, 400 MHz) δ 8.77 (s, 2H), 7.61 (q, 1H, J=8 Hz), 7.02 (m, 2H), 6.55 (s, 1H), 5.44 (s, 2H), 5.30 (s, 2H), 2.47 (s, 3H); ES-HRMS m/z 447.0267 (M+H calcd for C₁₉H₁₃N₄O₄F₂Br requires 447.0263).

Further Non-limiting Compounds

The following compounds can be prepared similarly using the compound (3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2(methylsulfonyl)pyrimidin-5-yl]methyl}pyridin-2(1H)-one) from Example 800.

Example No. R1
800-A       —O(CH2)nR2
800-B       —NH(CH2)nR2
800-C       —N(CH3)(CH2)nR2
800-D       —S(CH2)nR2,
800-E       —SO2(CH2)nR2
800-F
800-G
800-H
800-I
800-J
800-K

n=2, 3, 4; R₂=H, OH, NH₂, NHR₃, CONHR₃, OR₃; R₃=H, CH₃, CH(CH₃)₂.

The non-limiting compounds in the following table can also be made from the intermediate (3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2(methylsulfonyl) pyrimidin-5-yl]methyl}pyridin-2(1H)-one) by treatment with ZnBrCH₂COOt-Bu, hydrolysis and coupling with the appropriate amine.

Example R
800-L   CH2CONH2
800-M   CH2CONHCH3
800-N   CH2CONH(CH3)2
800-O   CH2CONH(CH2)nNH2
800-P   CH2CONH(CH2)nNHCH3

n=1-3

Example 806

1-{[2-(aminomethyl)pyrimidin-5-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

In a Fischer-Porter bottle, added a solution of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile (Example 805 above) (0.40 g, 0.89 mmol) in ethyl acetate/acetic acid ((3:1 v/v) (20 ml)). Flushed the solution with nitrogen then added palladium catalyst (0.18 g, 10% Pd/C). The bottle was sealed and evacuated. The system was purged with hydrogen gas (2×15 psi) to check for leaks. The reaction was charged with hydrogen (15 psi) and stirred at room temperature for 2 h. The system was evacuated and flushed with nitrogen. The reaction was filtered and the catalyst was carefully washed with fresh ethyl acetate. The filtrate was concentrated under reduced pressure and the residue was purified by reverse phase HPLC using a 10-90% acetonitrile in water (30 min. gradient) at a 100 ml/min flow rate to afford (after lyophilization) the salt of the desired compound (0.35 g, 70% yield). ¹H-NMR (CD₃OD, 400 MHz) δ 8.71 (s, 2H), 7.61 (q, 1H, J=8 Hz), 7.02 (m, 2H), 6.55 (s, 1H), 5.40 (s, 2H), 5.30 (s, 2H), 4.35, (s, 2H), 2.49 (s, 3H); ES-HRMS m/z 447.0255/453.0543 (M+H calcd for C₁₉H₁₈N₄O₂F₂Br requires 447.0263).

Example 807

N-1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)methyl]glycinamide

To a cold solution of 1-{[2-(aminomethyl)pyrimidin-5-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.1634 g, 0.36 mmol) in anhydrous DMF (5 mL) was added NMM (0.1 mL) followed by the addition of t-Boc glycine-N-hydroxysuccinimide ester (0.0987 g, 0.36 mmol). The reaction mixture was stirred at room temperature for 2.5 h. The reaction was diluted with water and extracted with ethyl acetate. The organic extracts were concentrated and the Boc group was removed with TFA (2 mL). The residue was diluted with acetonitrile and water and purified by reverse phase HPLC using a 10-90% acetonitrile in water (30 min. gradient) at a 70 ml/min flow rate to afford (after lyophilization) the salt of the desired compound (0.040 g). ¹H-NMR (CD₃OD, 400 MHz) δ 8.64 (s, 2H), 7.61 (q, 1H, J=8 Hz), 7.02 (m, 2H), 6.53 (s, 1H), 5.38 (s, 2H), 5.29 (s, 2H), 4.64, (s, 2H), 3.76 (s, 2H), 2.47 (s, 3H); ES-HRMS m/z 508.0822/(M+H calcd for C₂₁H₂₁N₅O₃F₂Br requires 508.0790).

Example 808

N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)methyl]-2-hydroxyacetamide

To a cold solution of 1-{[2-(aminomethyl)pyrimidin-5-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (0.130 g, 0.23 mmol) in anhydrous DMF (5 mL) was added NMM (0.06 mL) followed by the addition of acetoxyacetyl chloride (0.026 mL, 0.23 mmol). The reaction mixture was stirred cold to room temperature for 3 h. The solvent was removed and the residue was hydrolyzed to the alcohol with 1 N NaOH (3 mL). The reaction mixture was stirred at room temperature for 1.5 h. The residue was diluted with acetonitrile and water (TFA) and purified by reverse phase HPLC using a 10-90% acetonitrile in water (30 min. gradient) at a 70 ml/min flow rate to afford (after lyophilization) the salt of the desired compound (0.080 g). The TFA salt was washed with NaHCO₃ and water and extracted with MeCl₂. The solvent was removed in vacuo to afford the desired product (0.055 g) as a white solid. ¹H-NMR (CD₃OD, 400 MHz) δ 8.64 (s, 2H), 7.61 (q, 1H, J=8 Hz), 7.04 (m, 2H), 6.52 (s, 1H), 5.39 (s, 2H), 5.29 (s, 2H), 4.63, (s, 2H), 4.035 (s, 2H), 2.46 (s, 3H); ES-HRMS m/z 509.0621 (M+H calcd for C₂₁H₂₀N₄O₄F₂Br requires 509.0630).

The following table of non-limiting compounds can be made from the compound below (Example 807) using similar and/or known methodology.

Example R
807-A   CH2NHCONH2
807-B   CH2NHCO(CH2)2NH2
807-C   CH2NHCH3
807-D   CH2N(CH3)2
807-E   CH2NHSO2(C1-C3 alkyl)
807-F   CH2NHSO2 aryl
807-G   CH2NHCOCH(alkyl)NH2
807-H   CH2NHCOCH(CH2OH)NH2
807-I   CH2OCONH2
807-J   CH2O(CH2)2NH2

Example 809

5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carboxamide

To a solution of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile (0.20, 0.44 mmol) in anhydrous THF (5 mL) was added potassium trimethylsilanolate (0.114 g, 0.88 mmol). The reaction mixture was heated at 60° C. for 4 h. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic extracts were concentrated and the residue was purified by reverse phase HPLC using a 10-90% acetonitrile in water (30 min. gradient) at a 70 mL/min flow rate. The TFA salt was washed with NaHCO₃ and water and extracted with ethyl acetate. The solvent was removed in vacuo to afford the desired product (0.020 g) as a white solid. ¹H-NMR (CD₃OD, 400 MHz) δ 8.78 (s, 2H), 7.62 (q, 1H, J=8 Hz), 7.02 (m, 2H), 6.55 (s, 1H), 5.47 (s, 2H), 5.30 (s, 2H), 2.47 (s, 3H); ES-HRMS m/z 465.0394 (M+H calcd for C₁₉H₁₆N₄O₃F₂Br requires 465.0368).

The following table of non-limiting compounds can be made from the following compound (Example 809) by hydrolysis to the acid and coupling with the appropriate amine.

Example R
809-A   CONHCH3
809-B   CONH2
809-C   CON(CH3)2
809-D   CONH(CH2)nNH2
809-E   CONH(CH2)nNHCH3
809-F   CONH(CH2)nN(CH3)2

n=1-3

Example 810

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzamide

Step 1: Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzamide

4-Hydroxy-6-methyl-2-pyrone (10.0 g, 78.7 mmol) and 4-bromo-2-(trifluoromethyl)aniline (25 g, 104.1 mmol) were suspended in 25 ml of 1,2-dichlorobenzene in a 250 ml, 3-necked, round bottom flask equipped with a J-Kem temperature controller probe, a Dean-Stark trap, and a heating mantle. The reaction was heated to 165° C. for 15 min., during which some water and 1,2-dichlorobenzene was collected in the Dean-Stark trap. The reaction was allowed to cool to about 80° C. Toluene (100 mL) was added to the reaction with stirring. The reaction was allowed to stand for 16 h. at room temperature and a precipitate formed. The precipitate was filtered and washed 3 times with toluene, 3 times with hot water to remove excess pyrone, and dried in vacuo to give a solid (9 g, 33%). ¹H NMR (400 MHz, Acetone-d₆) δ 8.02 (m, 2H), 7.43 (d, J=8.19 Hz, 1H), 5.93 (m, 1H), 5.62 (d, J=2.42 Hz, 1H), 1.91 (s, 3H). LC/MS, t_r=2.54 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 348 (M+H).

Step 2: Preparation of (4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzamide

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzamide (from Step 1) (7.5 g, 21.6 mmol) was stirred at 0° C. with 2,4-difluorobenzyl bromide (2.78 ml, 21.6 mmol) and K₂CO₃ (3.5 g, 25.3 mmol) in 80 mL of dimethylformamide. The reaction was warmed to room temperature and stirred overnight. 300 mL of water was added into the reaction. The resulting mixture was extracted with ethyl acetate (500 ml). The ethyl acetate solution was dried over MgSO₄ and evaporated to dryness. The residue was crystallized overnight from ethyl acetate and hexane to afford white solid (7.3 g, 71%). LC/MS, t_r=3.16 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 474 (M+H).

Step 3: Preparation of Methyl 4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoate

Isopropyl magnesium chloride (2 M solution in THF) (7.5 ml, 15 mmol) was added into (4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzamide (from Step 2) (6 g, 12.6 mmol) in anhydrous THF at room temperature under nitrogen. After 2 h., N-methyl morpholine (2.8 ml, 25 mmol) was added into the reaction and followed by slow addition of methyl chloroformate (1.5 ml, 19 mmol). The reaction was stirred at room temperature for 16 h. 300 mL of water was added into the reaction. The resulting mixture was extracted with ethyl acetate (500 mL). The ethyl acetate solution was dried over MgSO₄ and evaporated to dryness to obtain 5.5 g of crude residue. The residue was purified using Gilson preparative LC system to afford white solid (1.5 g, 26%). LC/MS, t_r=3.05 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 454 (M+H).

Step 4: Preparation of 4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoic Acid

2.5 N NaOH solution (1.5 mL, 3.75 mmol) was added to methyl 4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoate (from Step 3) (1.1 g, 2.4 mmol) in 100 mL of 9:1 THF/water at room temperature. The reaction was stirred at room temperature for 16 h. 200 mL of water was added into the reaction. The resulting solution was acidified to pH 2 using concentrated hydrochloric acid. The resulting suspension was extracted with ethyl acetate (500 mL). The ethyl acetate solution was dried over MgSO₄ and evaporated to afford white solid (0.85 g, 80%). LC/MS, t_r=2.68 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50 C). ES-MS m/z 440 (M+H).

Step 5: Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoic Acid

N-Bromo succinimide (0.45 g, 2.5 mmol) was added into 4-[4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoic acid (from Step 4) (0.85 g, 1.9 mmol) in 15 mL of dichloromethane at room temperature. The reaction was stirred at room temperature for 16 h. 300 mL of water was added into the reaction. The resulting mixture was extracted with ethyl acetate (2×500 mL). The combined ethyl acetate solution was dried over MgSO₄ and evaporated to a dry residue. The residue was crystallized from ethyl acetate and hexane to afford white solid (0.82 g, 82%). ¹H NMR (400 MHz, CD₃OD) δ 8.47 (br s, 1H), 8.42 (dd, J=6.58, 1.47 Hz, 1H), 7.62 (m, 2H), 7.04 (m, 2H), 6.65 (s, 1H), 5.36 (s, 2H), 2.01 (s, 3H). LC/MS, t_r=2.77 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 518 (M+H). ES-HRMS m/z 518.0017 (M+H calcd for C₂₁H₁₄BrF₅NO₄ requires 518.0021).

Step 6: Preparation of the title compound. 2-chloro-4,6-dimethoxy-1,3,5-triazine (0.14 g, 0.81 mmol) was added into the mixture of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoic acid (from Step 5) (0.35 g, 0.67 mmol) and N-methyl morpholine (0.22 ml, 2.0 mmol) in 10 mL of THF. The mixture was stirred for 1 h. Ammonium hydroxide (28%, 1.5 ml) was added into the reaction and continued stirring for additional 16 h. 150 mL of water was added into the reaction and the resulting mixture was extracted with ethyl acetate (2×300 mL). The combined ethyl acetate solution was dried over MgSO₄ and evaporated to dried residue. The residue was crystallized from ethyl acetate and hexane to afford white solid (0.32 g, 92%). ¹H NMR (400 MHz, CDCl₃) δ 8.29 (s, 1H), 8.09 (app dd, J=6.72, 1.34 Hz, 1H), 7.59 (app dt, J=8.46, 6.31 Hz, 1H), 7.44 (br s, 1H), 7.19 (d, J=8.19 Hz, 1H), 6.99 (m, 1H), 6.88 (m, 1H), 6.17 (s, 1H), 5.27 (d, J=2.55 Hz, 2H), 1.91(s, 3H). LC/MS, t_r=2.54 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 517 (M+H). ES-HRMS m/z 517.0186 (M+H calcd for C₂₁H₁₅BrF₅N₂O₃ requires 517.0181).

Example 811

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-3-(trifluoromethyl)benzamide

1-[3-(dimthylamino)propyl]3-ethyl carbodiimide hydrogen chloride (88 mg, 0.46 mmol) was added into the mixture of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoic acid (from Example 810, step 5 above) (200 mg, 0.38 mmol), 1-hydroxy benzotriazole (62 mg, 0.46 mmol) and N-methyl morpholine (0.15 ml, 1.36 mmol) in 2.5 ml of dimethylformamide. The mixture was stirred for 1 h. Methylamine (2 M solution in THF) (2.5 ml, 0.5 mmol) was added into the mixture and continued stirring for 16 h. 150 ml of water was added into the reaction and white precipitate came out. Filtered and dried to obtain the white solid (155 mg, 77%). ¹H NMR (400 MHz, CDCl3) δ 8.21 (s, 1H), 8.01 (app d, J=8.05 Hz, 1H), 7.59 (app dt, J=8.46, 6.45 Hz, 1H), 7.42 (m, 1H), 7.18 (d, J=8.19 Hz, 1H), 6.97 (m, 1H), 6.90 (m, 1H), 6.16 (s, 1H), 5.26 (br s, 2H), 2.90 (d, J=4.56 Hz, 3H), 1.90 (s, 3H). LC/MS, t_r=2.66 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 531 (M+H). ES-HRMS m/z 531.0354 (M+H calcd for C₂₂H₁₇BrF₅N₂O₃ requires 531.0337).

Example 812

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N-dimethyl-3-(trifluoromethyl)benzamide

1-[3-(dimthylamino)propyl]3-ethyl carbodiimide hydrogen chloride (76 mg, 0.4 mmol) was added into the mixture of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoic acid (from Example 810, step 5 above) (175 mg, 0.33 mmol), 1-hydroxy benzotriazole (55 mg, 0.4 mmol) and N-methyl morpholine (0.15 ml, 1.36 mmol) in 2.5 ml of dimethylformamide. The mixture was stirred for 1 h. Dimethylamine (2 M solution in THF) (2.5 ml, 0.5 mmol) was added into the mixture and continued stirring for 16 h. 150 ml of water was added into the reaction and white precipitate came out. Filtered and dried to obtain the white solid (135 mg, 75%). ¹H NMR (400 MHz, CDCl3) δ 7.86 (app d, J=1.47 Hz, 1H), 7.72 (app dd, J=6.44, 1.48 Hz, 1H), 7.58 (app dt, J=8.46, 6.45 Hz, 1H), 7.30 (m, 1H), 6.95 (m, 1H), 6.85 (m, 1H), 6.11 (s, 1H), 5.24 (br s, 2H), 3.12 (s, 3H), 2.99 (s, 3H), 1.94 (s, 3H). LC/MS, t_r=2.70 min. (5 to 95% acetonitrile/water over 5 min. at 1 m/min with detection 254 nm, at 50° C.). ES-MS m/z 545 (M+H). ES-HRMS nm/z 545.0503 (M+H calcd for C₂₃H₁₉BrF₅N₂O₃ requires 545.0494).

Example 813

5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carboxamide

Step 1: Preparation of 4-methyl-2-(methylthio)pyrimidin-5-amine

Ethyl 4-methyl-2-(methylthio)pyrimidine-5-carboxylate (prepared similarly to the compound of Example 799, step 1) (5 g, 23.6 mmol) was added into the 100 ml of 9:1 THF/water. NaOH solution (2.5 N, 10 ml, 25 mmol) was added into the reaction and the reaction was stirred for 16 h. The solvent was evaporated to a dry residue to which 75 ml of acetonitrile was added, followed by addition of 50 ml of tert-butanol and diphenylphosphoryl azide (8.5 ml, 40 mmol). The mixture was heated to 90° C. for 16 h. The white suspension was filtered and the filtrate was evaporated to dried residue. The residue was added 300 ml of water and 500 ml of ethyl acetate. The organic layer was isolated and extracted several times with 500 ml of ethyl acetate. The combined ethyl acetate solution was dried over MgSO₄ and evaporated to a dry residue. This residue was dissolved in minimal amount of dichloromethane and loaded onto a bed of activated alumina and eluted with 3 L of dichloromethane. The dichloromethane solution was evaporated to a dry residue. HCl (4N) in 1,4-dioxane (50 ml) was added into the residue with stirring. After 3 h., diethyl ether (200 ml) was added to the reaction. The reaction stood for 1 h., and was filtered to isolate the formed solid. The solid was dissolved in 20 ml of water and was basified with saturated sodium bicarbonate solution. The basic solution was extracted with ethyl acetate (2×300 ml). The combined ethyl acetate solution was dried over MgSO₄ and evaporated to an amber oil (2.2 g, 60%). LC/MS, t_r=0.58 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 156 (M+H).

Step 2: Preparation of 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-methyl-2-(methylthio)pyrimidin-5-yl]pyridin-2(1H)-one

4-methyl-2-(methylthio)pyrimidin-5-amine (from Step 1) (2 g, 12.9 mmol) was added into 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione (Monatshefte fuer Chemie, 113, 1213-6, 1982) (3.5 g, 15.3 mmol) in 100 ml of 1,4-dioxane. The mixture was heated to 100° C. for 16 h. The reaction was cooled to room temperature and HCl in 1,4-dioxane (4N, 10 ml, 40 mmol) was added to the reaction. After 1 h. of stirring, the reaction was evaporated to a dry residue. The residue was added into 2,4-difluorobenzyl bromide (1.9 ml, 15 mmol) and potassium carbonate (10 g, 72.5 mmol) in 30 ml of dimethylformamide. The reaction was stirred for 16 h. To the reaction was added 150 ml of water and the resulting mixture was extracted with ethyl acetate (2×300 ml). The combined ethyl acetate solution was dried over MgSO₄ and evaporated to a crude brown oil (4.5 g, 89%). LC/MS, t_r=2.53 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 390 (M+H).

Step 3: Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-methyl-2-(methylsulfonyl)pyrimidin-5-yl]pyridin-2(1H)-one

N-bromo succinimide (3 g, 16.9 mmol) was added into a 100 mL dichloromethane solution of 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-methyl-2-(methylthio) pyrimidin-5-yl]pyridin-2(1H)-one (from Step 2) (5.5 g, 14.1 mmol). The reaction was stirred for 1 h. Water (30 mL) and magnesium monoperoxyphthalate hexahydrate (17.5 g, 35 mmol) was then added. The reaction was stirred vigorously for 16 h. 300 ml of water was added into the reaction and the resulting mixture was extracted with dichloromethane (2×700 ml). The combined organic solution was dried over MgSO₄ and evaporated to crude residue. The crude residue was purified using Waters Prep 2000 system to obtain the compound (1.1 g, 16%). ¹H NMR (400 MHz, CDCl3) δ 8.59 (s, 1H), 7.54 (app dt, J=8.46, 6.45 Hz, 1H), 6.93 (m, 1H), 6.85 (m, 1H), 6.25 (s, 1H), 5.25 (s, 2H), 3.35 (s, 3H), 2.42 (s, 3H), 1.93 (s, 3H). LC/MS, t_r=2.36 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 500 (M+H). ES-HRMS m/z 500.0090 (M+H calcd for C₁₉H₁₇BrF₂N₃O₄S requires 500.0086).

Step 4: Preparation of 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carbonitrile

Potassium cyanide (0.24 g, 3.7 mmol) was added into 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-methyl-2-(methylsulfonyl)pyrimidin-5-yl]pyridin-2(1H)-one (from Step 3) (0.97 g, 1.93 mmol) was added into 15 ml of dimethylformamide. The reaction was stirred for 16 h. 200 ml of water was added into the reaction and the resulting mixture was extracted with ethyl acetate (2×300 ml). The combined organic solution was dried over MgSO₄ and evaporated to a dry residue. The crude residue was crystallized from methanol and ether to obtain the compound (0.8 g, 92%). ¹H NMR (400 MHz, CDCl3) δ 8.52 (s, 1H), 7.59 (app dt, J=8.46, 6.45 Hz, 1H), 6.97 (m, 1H), 6.88 (m, 1H), 6.21 (s, 1H), 5.28 (s, 2H), 2.41 (s, 3H), 1.95 (s, 3H). LC/MS, t_r=2.65 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 447 (M+H). ES-HRMS m/z 447.0257 (M+H calcd for C₁₉H₁₄BrF₂N₄O₂ requires 447.0263).

Step 5: Preparation of 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carboxylic Acid

5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carbonitrile (from Step 4) (0.7 g, 1.56 mmol) was added into 20 ml of methanol and 20 ml of hydrochloric acid. The reaction was heated to 80° C. for 2 h. The reaction was cooled to room temperature and 300 ml saturated sodium carbonate solution was added. The mixture was stirred for 1 h. and neutralized with aqueous HCl. The mixture was extracted with ethyl acetate (2×300 ml). The combined organic solution was dried over MgSO₄ and evaporated to a dry residue. The crude residue was crystallized from methanol, ethyl acetate and hexane to obtain the compound (0.45 g, 62%). ¹H NMR (400 MHz, CDOD) δ 8.75 (s, 1H), 7.62 (m, 1H), 7.00 (m, 2H), 6.67 (s, 1H), 5.36 (s, 2H), 2.40 (s, 3H), 2.03 (s, 3H). LC/MS, t_r=2.16 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS nz/z 466 (M+H). ES-HRMS m/z 466.0206 (M+H calcd for C₁₉H₁₅BrF₂N₃O₄ requires 466.0209).

Step 6: Preparation of the title compound. 2-chloro-4,6-dimethoxy-1,3,5-triazine (0.10 g, 0.56 mmol) was added into a mixture of 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carboxylic acid (from Step 5) (0.22 g, 0.47 mmol) and N-methyl morpholine (0.22 ml, 2.0 mmol) in 10 ml of tetrahydrofuran. The mixture was stirred for 1 h. Ammonium hydroxide (28%, 1.5 ml) was added into the reaction and stirring continued for additional 16 h. Water (150 ml) was added to the reaction and the resulting mixture was extracted with ethyl acetate (2×300 ml). The combined ethyl acetate solution was dried over MgSO₄ and evaporated to dryness. The resulting residue was crystallized from methanol, dichloromethane and hexane to afford yellow needle-like solid (0.16 g, 73%). ¹H NMR (400 MHz, CDOD) δ 8.66 (s, 1H), 7.59 (m, 1H), 6.96 (m, 2H), 6.57 (s, 1H), 5.33 (s, 2H), 2.39 (s, 3H), 2.01 (s, 3H). LC/MS, t_r=2.16 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 465 (M+H). ES-HRMS m/z 465.0363 (M+H calcd for C₁₉H₁₆BrF₂N₄O₃ requires 465.0368).

Example 814

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl Carbamate

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one (500 mg, 1.15 mmol) was stirred with trichloroacetyl isocyanate (2.4 ml, 1.27 mmol) in 5 ml of methylene chloride at room temperature. After 1 h., the reaction was quenched with ammonium hydroxide solution and was stirred vigorously at room temperature for 1 h. The reaction was then poured into 100 ml of cold water and the resulting precipitate was filtered, washed with diethyl ether and dried in vacuo to give a white solid (425 mg, 77%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.66 (app q, J=7.92 Hz, 1H), 7.45 (d, J=8.19 Hz, 2H), 7.33 (dt, J=9.87, 2.15 Hz, 1H), 7.24 (d, J=8.19 Hz, 2H), 7.16 (dt, J=8.12, 2.19 Hz, 1H), 6.81-6.38 (br s, 2H), 6.64 (s, 1H), 5.31 (s, 2H), 5.03 (s, 2H), 1.92 (s, 3H); LC/MS, t_r=2.41 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS nm/z 479 (M+H). ES-HRMS nm/z 479.0387 (M+H calcd for C₂₁H₁₈BrF₂N₂O₄ requires 479.0413).

Example 815

N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-2-hydroxy-2-methylpropanamide

Step 1: Preparation of Methyl 4-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate

Methyl 4-(4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate (see Example 202, step 1) (10.0 g, 38.6 mmol) was stirred at room temperature with N-bromosuccinimide (6.87 g, 38.6 mmol) in 80 ml of N,N-dimethylformamide and 100 ml of methylene chloride. After stirring as a slurry overnight, the precipitate was filtered, washed with diethyl ether, and dried in vacuo to give a white solid (10.38 g, 80%). ¹H NMR (400 MHz, DMSO-d₆) δ 11.53 (s, 1H), 8.05 (d, J=8.46 Hz, 2H), 7.39 (d, J=8.45 Hz, 2H), 6.11 (s, 1H), 3.86 (s, 3H), 1.81 (s, 3H); LC/MS, t_r=1.69 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 338 (M+H). ES-HRMS m/z 338.0044 (M+H calcd for C₁₄H₁₃BrNO₄ requires 338.0022).

Step 2: Preparation of Methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate

Methyl 4-(3-bromo-4-hydroxy-6-methyl-2-oxopyridin-1(2H)-yl)benzoate (from Step 1) (10.25 g, 30.3 mmol) was stirred vigorously with 2,4-difluorobenzylbromide (3.89 ml, 30.3 mmol) and K₂CO₃ (6.28 g, 45.4 mmol) in 50 ml of N,N-dimethylformamide at room temperature for 1.5 h. The reaction was then poured into 1 L of cold water and the resulting precipitate was filtered, washed with water and diethyl ether, and dried in vacuo to yield a white solid (10.13 g, 72%). See Example 202.

Step 3: Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoic acid

See the protocol detailed in Example 203.

Step 4: Preparation of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide

This compound can be synthesized according to the protocol detailed in Example 244.

Step 5: Preparation of 1-[4-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzamide (from Step 4) (1.82 g, 4.05 mmol) was added to a solution of 2 M borane-dimethylsulfide complex in tetrahydrofuran (6.07 ml, 12.15 mmol) in 12 ml tetrahydrofuran at 0° C. The reaction was allowed to warm to room temperature with stirring. After stirring for 4 days, ice chips were added to quench the reaction. The reaction was extracted 2 times with ethyl acetate, which removed some non-polar impurities. The aqueous layer was then extracted 5 times with n-butanol and the combined organic layers were evaporated. The resulting solid was washed with diethyl ether and dried in vacuo to give a white solid (865 mg, 49%). ¹H NMR (400 MHz, DMSO-d₆) δ 7.71 (app q, J=7.99 Hz, 1H), 7.50 (d, J=8.26 Hz, 2H), 7.38 (dt, J=9.87, 2.15 Hz, 1H), 7.25-7.19 (m, 3H), 6.67 (s, 1H), 5.36 (s, 2H), 3.82 (s, 2H), 2.45 (br s, 2H), 1.97 (s, 3H); LC/MS, t_r=2.03 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 435 (M+H). ES-HRMS m/z 435.0508 (M+H calcd for C₂₀H₁₈BrF₂N₂O₂ requires 435.0514).

Step 6: Preparation of the Title Compound

1-[4-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one (from Step 5) (400 mg, 0.92 mmol) was dissolved in 8 ml of N,N-dimethylformamide and 5 ml of methylene chloride. 2-hydroxyisobutyric acid (96 mg, 0.92 mmol) was added, followed, in order, by EDCI (225 mg, 1.15 mmol), 1-hydroxybenzotriazole (155.4 mg, 1.15 mmol) and triethylamine (257 μL, 1.84 mmol). The reaction was stirred at room temperature overnight. The methylene chloride was evaporated and the reaction was then poured into 200 ml of cold water. The resulting solid was filtered and washed with water and diethyl ether and dried in vacuo to give a white solid (276 mg, 53%). ¹H NMR (400 MHz, DMSO-d₆) δ 8.30 (t, J=6.38 Hz, 1H), 7.67 (app q, J=7.82 Hz, 1H), 7.35-7.26 (m, 3H), 7.18-7.14 (m, 3H), 6.62 (s, 1H), 5.42 (s, 1H), 5.31 (s, 2H), 4.31 (d, J=6.24 Hz, 2H), 1.91 (s, 3H), 1.26 (s, 6H); LC/MS, t_r=2.36 min. (5 to 95% acetonitrile/water over 5 min. at 1 my/min, at 254 nm, at 50° C.), ES-MS m/z 521 (M+H). ES-HRMS m/z 521.0876 (M+H calcd for C₂₄H₂₄BrF₂N₂O₄ requires 521.0882).

Example 816

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)phenyl]-6-methylpyridin-2(1H)-one

Step 1: Preparation of 4-hydroxy-6-methyl-1-(4-vinylphenyl)pyridin-2(1H)-one

5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione (43.1 g, 189 mmol) and 4-vinylaniline (15.0 g, 125.9 mmol) were dissolved in 500 ml 1,4-dioxane and heated to reflux for 45 min. Methane sulphonic acid (8.17 g, 125.9 mmol) was added and refluxed for 1 h. The reaction was allowed to cool to room temperature and stand overnight. The reaction was added to an amount of water and extracted with ethyl acetate and n-butanol. The combined organic layers were dried over MgSO₄ and evaporated. The resulting oil was triturated with ethyl acetate/diethyl ether to obtain a solid. The resulting precipitate was filtered and washed with ethyl acetate, acetonitrile, acetone and diethyl ether and dried in vacuo to give a tan solid (8.57 g, 20% yield). ¹H NMR (300 MHz, DMSO-d₆) δ 10.65 (br s, 1H), 7.59 (d, J=8.46 Hz, 2H), 7.18 (d, J=8.26 Hz, 2H), 6.82 (dd, J=17.72, 10.88 Hz, 1H), 5.92 (d, J=17.52 Hz, 1H), 5.92 (d, J=2.41 Hz, 1H), 5.58 (d, J=2.61 Hz, 1H), 5.36 (d, J=10.88 Hz, 1H), 1.87 (s, 3H); LC/MS, t_r=1.85 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 228 (M+H). ES-HRMS m/z 228.1023 (M+H calcd for C₁₄H₁₄NO₂ requires 228.1019).

Step 2: Preparation of 3-bromo-4-hydroxy-6-methyl-1-(4-vinylphenyl)pyridin-2(1H)-one

4-hydroxy-6-methyl-1-(4-vinylphenyl)pyridin-2(1H)-one (from Step 1) (8.0 g, 35.2 mmol) was stirred at room temperature with N-bromosuccinimide (6.26 g, 35.2 mmol) in 75 ml of N,N-dimethylformamide. After stirring overnight, the reaction was poured into cold water. The resulting precipitate was filtered, washed with water and diethyl ether, and dried in vacuo to give a white solid (7.99 g, 74%). ¹H NMR (300 MHz, DMSO-d₆) δ 11.41 (br s, 1H), 7.62 (d, J=8.46 Hz, 2H), 7.23 (d, J=8.45 Hz, 2H), 6.82 (dd, J=17.72, 11.08 Hz, 1H), 6.09 (s, 1H), 5.94 (d, J=17.52 Hz, 1H), 5.37 (d, J=11.08 Hz, 1H), 1.88 (s, 3H); LC/MS, t_r=1.90 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS it/z 306 (M+H). ES-HRMS nm/z 306.0103 (M+H calcd for C₁₄H₁₃BrNO₂ requires 306.0124).

Step 3: Preparation of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(4-vinylphenyl)pyridin-2(1H)-one

3-Bromo-4-hydroxy-6-methyl-1-(4-vinylphenyl)pyridin-2(1H)-one (from Step 2) (7.75 g, 25.3 mmol) was stirred vigorously with 2,4-difluorobenzylbromide (3.25 ml, 25.3 mmol) and K₂CO₃ (5.25 g, 38.0 mmol) in 40 ml of N,N-dimethylformamide at room temperature overnight. The reaction was then poured into 1 L of cold water and the resulting precipitate was filtered, washed with water and ethyl acetate, and dried in vacuo to yield a white solid (2.52 g, 23%). ¹H NMR (300 MHz, DMSO-d₆) δ 7.71 (app q, J=7.65 Hz, 1H), 7.64 (d, J=8.26 Hz, 2H), 7.38 (dt, J=9.97, 2.42 Hz, 1H), 7.27 (d, J=8.26 Hz, 2H), 7.23 (app t, J=8.26 Hz, 1H), 6.84 (dd, J=17.72, 11.07 Hz, 1H), 6.69 (s, 1H), 5.96 (d, J=17.72 Hz, 1H), 5.40-5.37 (m, 3H), 1.99 (s, 3H); LC/MS, t_r=2.96 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 432 (M+H). ES-HR/MS m/z 432.0390 (M+H calcd for C₂₁H₁₇BrF₂NO₂ requires 432.0405).

Step 4: Preparation of the Title Compound

3-Bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(4-vinylphenyl)pyridin-2(1H)-one (from Step 3) (500 mg, 1.16 mmol) was stirred as a suspension in 13 ml acetone and 3.25 ml water. 4-methylmorpholine N-oxide (311.6 mg, 2.66 mmol) was added, followed by 4% w/w water solution of OSO₄ (0.1 ml, 1.3 mol %) and the reaction was stirred at room temperature overnight. The reaction was diluted with 150 ml of ethyl acetate, washed with water, dried over MgSO₄ and evaporated to near dryness. The resulting precipitate was filtered, washed with diethyl ether and dried in vacuo to yield a white solid (297 mg, 55%). ¹H NMR (300 MHz, DMSO-d₆) δ 7.71 (app q, J=7.92 Hz, 1H), 7.52-7.48 (m, 2H), 7.38 (dt, J=9.87, 2.42 Hz, 1H), 7.24-7.20 (m, 3H), 6.67 (s, 1H), 5.40 (d, J=5.43 Hz, 1H), 5.36 (m, 2H), 4.80 (t, J=5.74 Hz, 1H), 4.63 (dd, J=10.07, 5.44 Hz, 1H), 3.51 (t, J=5.74 Hz, 2H), 1.96 (s, 3H); LC/MS, t_r=2.24 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min, at 254 nm, at 50° C.), ES-MS m/z 466 (M+H). ES-HR/MS m/z 466.0451 (M+H calcd for C₂₁H₁₉BrF₂NO₄ requires 466.0460).

Exmaple 817

3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(hydroxyl)benzamide

Step 1: Preparation of 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(tetrahydro-2H-pyran-2-yloxy)benzamide

The title compound of Step 1 was prepared by a procedure similar to the one described for the compound of Example 487, where O-(tetrahydro-2H-pyran-2-yl)hydroxylamine was used as the amine instead of ethanolamine to yield the desired product (350 mg, 56%). ¹H NMR (300 MHz, CDCl₃) δ 10.0-9.86 (m, 1H), 7.71-7.67 (m, 1H), 7.63-7.58 (m, 1H), 7.55 (br s, 1H), 7.32 (d, J=8.06 Hz, 1H), 7.04-6.98 (m, 1H), 6.96-6.89 (m, 1H), 6.23 (s, 1H), 5.31 (s, 2H), 5.10 (br s, 1H), 4.17-4.0 (m, 2H), 3.71-3.59 (dd, J=11.28, 26.78 Hz, 2H), 2.12 (s, 3H), 1.94 (s, 3H), 1.85-1.61 (m, 2H), 1.32-1.27 (m, 2H); LC/MS, t_r=2.67 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 519 (M+H).

Step 2: Preparation of the title compound. 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(tetrahydro-2H-pyran-2-yloxy)benzamide (from Step 1) (250 mg, 0.48 mmol) was stirred at room temperature with 12 N HCl (0.12 ml, 1.44 mmol) in 5 ml of dioxane for 2.0 h. Upon quenching the reaction with water, a precipitate formed and was collected. The precipitate was purified by dissolving it in ethyl acetate and triturating with diethyl ether. The precipitate was collected and dried to yield a white solid (50 mg, 24%). ¹H NMR (300 MHz, CD₃OD) δ 7.79 (d, J=7.93 Hz, 1H), 7.66 (app q, J=6.72, 1H), 7.52-7.51 (m, 2H), 7.07-7.02 (m, 2H), 5.35 (s, 2H), 2.07 (s, 3H), 2.00 (s, 3H); LC/MS, t_r=2.24 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 435 (M+H).

Example 818

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(tetrahydro-2H-pyran-2-yloxy)benzamide

The title compound was prepared by a procedure similar to the one described for the compound of Example 487, where O-(tetrahydro-2H-pyran-2-yl)hydroxylamine was used as the amine to yield the desired product (800 mg, 62%). ¹H NMR (400 MHz, CDCl₃) δ 10.12-9.96 (m, 1H), 7.62-7.56 (m, 1H), 7.51 (br s, 1H), 7.26 (m, 1H), 6.98-6.89 (m, 1H), 6.86-6.83 (m, 1H), 6.15 (s, 1H), 5.25 (s, 2H), 5.06 (d, J=14.24 Hz, 1H), 4.09-3.98 (m, 2H), 3.58 (dd, J=30.09, 11.55 Hz, 2H) 2.04 (d, J=9.94 Hz, 3H), 1.87 (s, 3H), 1.83-1.70 (m, 2H), 1.62-1.50 (m, 3H); LC/MS, t_r=2.73 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 563 (M+H). This compound can be converted to the N—OH analogue by hydrolysis with HCl.

Example 819

N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzyl}-2-hydroxyacetamide

Step 1: Preparation of 1-[5-(aminomethyl)-2-methylphenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one Hydrochloride

The title compound of Step 1 was prepared by the addition of 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide (2.0 g, 4.32 mmol) to a 0° C. solution of 1 M BH₃-THF (9.1 ml, 9.10 mmol). THF (20 ml) was added and the mixture was heated to reflux. No reaction was observed after 3 h. 2 M BH₃-DMS (10 ml) was added and the reaction mixture became completely soluble. After 2 additional hours, 6 N HCl was added to reaction. The organic solvent was removed in vacuo. The aqueous layer was made basic with 2.5 N NaOH and extracted with dichloromethane. The aqueous layer separated and the dichloromethane was removed in vacuo. The residue was taken up in acetonitrile. 1.0 N HCl in diethethyl ether was added to the acetonitrile mixture and the resulting precipitate was collected on a filter pad to yield the desired product (1.2 g, 53%). ¹H NMR (400 MHz, CD₃OD) δ 7.65 (app q, J=6.56 Hz, 1H), 7.50 (s, 1H), 7.49 (s, 1H), 7.24 (s, 1H), 7.07-7.02 (m, 2H), 6.68 (s, 1H)), 5.36 (s, 2H), 4.13 (s, 2H), 2.05 (s, 3H), 2.00 (s, 3H); LC/MS, t_r=1.96 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 450 (M+H).

Step 2: Preparation of the title compound. 1-[5-(aminomethyl)-2-methylphenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride (from Step 1) (500 mg, 1.03 mmol), glycolic acid, (94.3 mg, 1.24 mmol), EDC (192.5 mg, 1.24 mmol), HOBt (135.1 mg, 1.24 mmol), and N-methyl morpholine (0.45 ml, 4.12 mmol) were stirred together in DMF (10 ml) for 3 h. The reaction was quenched with saturated ammonium chloride (aq.) and extracted with dichloromethane. The dichloromethane layer was separated and dried over Na₂SO₄. The solvent was removed in vacuo. The residue was taken up in ethyl acetate and triturated with diethyl ether. The precipitate was collected on a filter pad to yield a white solid (325 mg, 62%). ¹H NMR (400 MHz, CDCl₃) δ 7.59 (app q, J=6.98 Hz, 1H), 7.28 (m, 2H), 6.98-6.94 (m, 2H), 6.84 (t, J=8.19 Hz, 1H), 6.14 (br s, 1H), 5.21 (s, 2H), 4.46 (dd, J=9.67, 5.91 Hz, 1H), 4.24 (dd, J=11.00, 5.24 Hz, 1H), 3.88 (dd, J=16.11, 11.14 Hz, 2H), 3.00 (m, 3H), 1.98 (s, 3H), 1.90 (s, 3H); LC/MS, t_r=2.35 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 507 (M+H).

Example 820

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-cyclopropylbenzamide

The title compound was prepared by a procedure similar to the one described for the compound of Example 487, where cyclopropylamine was used as the amine to yield the desired product (0.74 g, 57%). ¹H NMR (400 MHz, CDCl₃) δ 7.70 (dd, J=7.92, 1.75 Hz, 1H), 7.59 (app q, J=8.59 Hz, 1H), 7.50 (d, J=1.88, 1H), 7.31 (d, J=8.19, 1H), 6.95-6.90 (m, 2H), 6.78 (dt, J=8.73, 2.55 Hz, 1H), 6.13 (s, 1H), 6.18 (s, 1H), 5.24 (s, 2H), 2.68-2.62 (m, 1H), 2.06(s, 3H), 1.89 (s, 3H), 0.71-0.59 (m, 2H), 0.49-0.40 (m, 2H); LC/MS, t_r=2.59 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 503 (M+H).

Example 821

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-ethyl-4-methylbenzamide

The title compound was prepared by a procedure similar to the one described for Example 487, where ethylamine was used as the amine to yield the desired product (0.25 g, 19%). ¹H NMR (400 MHz, CDCl₃) δ 7.80 (dd, J=8.06, 1.48 Hz, 1H), 7.59 (app q, J=8.46 Hz, 1H), 7.51 (br s, 1H), 7.33 (d, J=7.92, 1H), 6.96-6.93 (m, 1H), 6.85-6.79 (m, 1H), 6.71-6.91 (m, 1H), 6.14 (s, 1H), 5.20 (s, 2H), 3.30 (m, 2H), 2.06 (s, 3H), 1.89 (s, 3H), 1.10 (t, J=7.25 Hz, 3H); LC/MS, t_r=2.45 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 491 (M+H).

Example 822

N-allyl-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide

The title compound was prepared by a procedure similar to the one described for Example 487, where allylamine was used as the amine to yield the desired product (0.55 g, 42%). ¹H NMR (400 MHz, CDCl₃) δ 7.76 (dd, J=6.18, 1.75 Hz, 1H), 7.60 (app q, J=8.46 Hz, 1H), 7.54 (d, J=1.75, 1H), 7.28 (d, J=8.06, 1H), 6.96-6.90 (m, 2H), 6.81 (dt, J=8.60, 2.55 Hz, 1H), 6.14 (s, 1H), 5.83-5.74 (m, 1H), 5.20 (s, 2H), 5.05 (dd, J=10.20, 1.34 Hz, 1H), 5.03 (dd, J=10.20, 1.34 Hz, 1H), 3.93-3.78 (m, 2H), 2.05 (s, 3H), 1.89 (s, 3H); LC/MS, t_r=2.65 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 503 (M+H).

Example 823

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-butyl-4-methylbenzamide

The title compound was prepared by a procedure similar to the one described for Example 487, where n-butylamine was used as the amine to yield the desired product (0.65 g, 50%). ¹H NMR (400 MHz, CDCl₃) δ 7.77 (dd, J=7.79, 1.75 Hz, 1H), 7.61 (app q, J=8.46 Hz, 1H), 7.49 (d, J=1.61, 1H), 7.34 (d, J=8.06, 1H), 6.97-6.93 (m, 1H), 6.83 (dt, J=8.73, 2.42 Hz, 1H), 6.55 (t, J=5.37 Hz, 1H) 6.12 (s, 1H), 5.21 (s, 2H), 3.28 (m, 2H), 2.07 (s, 3H), 1.90 (s, 3H), 1.45 (m, 2H), 1.32 (m, 2H), 0.90 (t, J=7.25 Hz, 3H); LC/MS, t_r=2.76 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.); ES-MS m/z 519 (M+H).

Example 824

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-isobutyl-4-methylbenzamide

The title compound was prepared by a procedure similar to the one described in Example 487, where isobutylamine was used as the amine to yield the desired product (0.60 g, 46%). ¹H NMR (400 MHz, CDCl₃) δ 7.75 (dd, J=7.92, 1.75 Hz, 1H), 7.60 (app q, J=8.46 Hz, 1H), 7.51 (d, J=1.75, 1H), 7.33 (d, J=8.06, 1H), 6.98-7.93 (m, 2H), 6.84 (dt, J=8.73, 2.42 Hz, 1H), 6.65 (t, J=5.77 Hz, 1H), 6.71 (s, 1H), 6.12 (s, 1H), 5.21 (s, 2H), 3.13 (m, 2H), 2.07 (s, 3H), 1.90 (s, 3H), 1.79, (m, 1H), 0.88 (dd, J=6.71, 1.21) Hz; LC/MS, t_r=2.76 min. (5 to 95% acetonitrile/water over 5 min. at 1 m/min with detection 254 nm, at 50° C.); ES-MS m/z 519 (M+H).

Example 825

(2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]but-2-enoic Acid

To a slurry of the ester from Example 460(940 mg, 2.1 mmol), in THF (4 mL) at r.t., was added a 2.5 N NaOH solution (1.0 mL). The resulting homogeneous solution was allowed to stir at r.t. overnight. The reaction was quenched by dropwise addition of a 3 N HCl solution until the pH was ˜4. The solvent was concentrated by passing N₂ gas over the reaction to give a white precipitate. The reaction was filtered to give a white solid which was washed with diethyl ether and dried to give an off-white solid (757 mg, 86%) of >95% purity. ¹H-NMR (DMSO_d6/300 MHz) δ 7.68 (app quar, J=8.7 Hz, 1H), 7.36 (dt, J=10.5, 2.4 Hz, 1H); 7.23-7.10 (m 1H); 6.90 (dt, J=15.9, 4.2 Hz, 1H), 6.60 (s, 1H), 5.45 (d, J=15.6 Hz, 1H), 5.32 (s, 2H), 4.90-4.80 (m, 2H), 2.32 (s, 3H). ES-HRMS m/z 414.0126 (M+H calcd for C₁₇H₁₅BrF₂NO₄=414.0147).

Example 826

(2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxy-2-methylpropyl)but-2-enamide

The title compound above was prepared similar to the method as described for the synthesis for the compound of Example 659. Starting from the acid described in Example 825 (300 mg, 0.72 mmol) and the appropriate amino alcohol, the desired product was obtained in 95% purity as a tan colored solid (225 mg, 55% yield). ¹H-NMR (DMSO_d6/300 MHz) δ 7.92 (t, J=6.0 Hz, 1H), 7.68 (q, J=8.7 Hz, 1H); 7.37 (dt, J=10.5, 2.4 Hz, 1H); 7.20 (dt, J=10.5, 1.8 Hz, 1H); 6.71 (dt, J=15.3, 4.2 Hz, 1H), 6.61 (s, 1H), 5.82 (d, J=15.6 Hz, 1H), 5.31 (s, 2H), 4.82 (d, J=2.4 Hz, 2H), 3.07 (d, J=6.9 Hz, 1H), 2.61 (d, J=6.0 Hz, 3H), 2.37 (s, 3H), 1.04 (s, 6H). ES-HRMS m/z 485.0875 (M+H calcd for C₂₁H₂₄BrF₂N₂O₄=485.0882).

Example 827

{5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2E)-4-hydroxybut-2-enyl]-6-oxo-1,6-dihydropyridin-2-yl}methyl Acetate

The title compound was prepared by adding cis-butene-1,4-diol (100 μl, 1.1 mmol) to a slurry of the compound from Example 832 (0.43 g, 1 mmol) in 5 ml of benzene. Grubbs catalyst, tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene][benzylidine]ruthenium(IV)chloride, (0.015 g, 0.05 mmol) was added to the reaction. The mixture was then heated to 60° C. After 3 h., the reaction was about 50-60% complete. Additional diol (200 ml) and Schrock catalyst (0.015 g) were added and the reaction was maintained at 60° C. for 12 h. The reaction was quenched by addition of water. The layers were separated and the organic layer was extracted with CH₂C₁₂ (4×). The organics were combined, dried, and concentrated in vacuo. The crude residue was purified by flash chromatography on a 35 g Michelle-Miller column. Eluting with hexanes-ethyl acetate (2:1→0:100) gave the desired product (0.21 g, 46%) as a tan solid. ¹H-NMR (DMSO_d6/500 MHz) δ 7.64 (q, J=8.5 Hz, 1H); 7.33 (dt, J=10.5, 2.5 Hz, 1H); 7.16 (dt, J=8.5, 2.0 Hz, 1H), 6.66 (s, 1H), 5.69-5.64 (m, 1H), 5.51 (dt, J=16.0, 4.5 Hz, 1H), 5.32 (s, 2H), 5.01 (s, 2H), 4.61 (d, J=4.5 Hz, 1H), 3.89 (d, J=3.5 Hz, 1H), 2.12 (s, 3H). ES-HRMS m/z 458.0392 (M+H calcd for C₁₉H₁₉BrF₂NO₅=458.0409).

Example 828

(2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxy-2-methylpropyl)but-2-enamide

The titled compound was prepared using a similar method to that described in Example 659. Starting from the acid described in Example 825 (315 mg, 0.76 mmol), the desired product was obtained in 90-95% purity as an off-white solid (250 mg, 68% yield). ¹H-NMR (DMSO_d6/300 MHz) δ 7.62 (q, J=6.3 Hz, 1H); 7.31 (dt, J=8.1, 2.1 Hz, 1H); 7.17-7.10 (m, 1H), 6.59 (dt, J=15.6, 3.9 Hz, 1H); 6.55 (s, 1H), 6.37 (d, J=11.4 Hz, 1H), 5.26 (s, 2H), 4.78 (d, J=3.0 Hz, 2H), 3.53-3.50 (m, 4H), 3.45-3.43 (m, 4H), 2.34 (s, 3H). ES-HRMS m/z 483.0700 (M+H calcd for C₂₁H₂₂BrF₂N₂O₄=483.0726).

Example 829

Methyl-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

A solution of the compound of Example 653 (1.4 g, 2.6 mmol) was slurried in methanol (13 mL). To this solution was added solid potassium carbonate (770 mg, 5.7 mmol). The mixture was stirred at room temperature. After 1.5 h., the reaction was poured into a flask containing deionized water. The resulting solid was filtered through a fritted funnel. The solid was dried under vacuum to give the desired product as an off-white solid (950 mg, 74% yield). ¹H NMR (300 MHz, DMSO_-d6) δ 8.00 (dd, J=8.1, 1.8 Hz, 1H), 7.79 (d, J=1.5 Hz, 1H), 7.72 (app q, J=6.9 Hz, 1H), 7.59 (d, J=8.1 Hz, 1H), 7.40 (dt, J=9.9, 2.4 Hz, 1H), 7.26-7.19 (m, 1H), 6.75 (s, 1H), 5.41 (s, 2H), 3.87 (s, 3H), 3.85 (AB quar, J=15.6 Hz, 2H), 2.06 (s, 3H). ES-HRMS nm/z 536.0484 (M+H calcd for C₂₄H₂₁NF₂BrO₆ requires 536.0515).

Example 830

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-5-vinylphenyl)pyridin-2(1H)-one

Step 1-Preperation of -1-(5-bromo-2-methylphenyl)-4-hydroxy-6-methylpyridin-2(1H)-one

To a 500 mL round-bottom flask containing 2-methyl, 5-bromo aniline (2.79 g, 15 mmol) was added 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione (5.0 g, 20.7 mmol). This mixture was then slurried in toluene (75 mL) along with a catalytic amount of p-toluenesulfonic acid and heated to reflux under a nitrogen environment for 2 h. The reaction was then allowed to cool to r.t., resulting in formation of a precipitate. The reaction mixture was further diluted with 50 ml ether and the solid was isolated by filtration of the reaction mixture. The solid was washed with diethyl ether to give the desired product (3.39 g, 77% yield) as a white solid. ¹H NMR (400 MHz, CDCl₃) δ 7.51 (dd, J=8.60, 2.19 Hz, 1H), 7.37 (d, J=2.01 Hz, 1H), 7.31 (d, J=8.23, 1H), 5.89 (dd, J=1.35, 0.97 Hz, 1H), 5.53 (d, J=2.53 Hz, 1H), 1.86 (s, 3H), 1.76 (s, 3H), ES-LCMS m/z 294 (M+H calcd for C₁₃H₁₃BrNO₂, requires 294).

Step 2: Preparation of 1-(5-bromo-2-methylphenyl) -4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one

In a 500 ml round-bottom flask, the compound from Step 1(12.6 g, 43.0 mmol) was dissolved in 180 ml of DMF. To this mixture was added anhydrous potassium carbonate (1.91 g, 13.83 mmol) followed by addition of 2,4-difluorobenzyl bromide (6.9 g, 50 mmol). The reaction was allowed to stir at room temperature overnight. The reaction was then poured into 300 ml of ice water. The aqueous solution was extracted with ethyl acetate (4×100 mL) and combined. The organic layer was washed with brine (2×100 mL), dried and concentrated in vacuo. The resulting solid was triturated with diethyl ether and filtered to yield a tan solid, which was used in the next step without further purification.

Step 3: Preparation of 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-5-vinylphenyl)pyridin-2(1H)-one

4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-5-vinylphenyl)pyridin-2(1H)-one was prepared by reacting the compound of Step 2 (3.0 g, 7.15 mmol) with vinyltributyl tin (2.64 ml, 9 mmol) via a Stille coupling procedure, similar to that described for Example 477 (step 3) to yield the desired product (4 g, 54% yield) after filtration through a plug of silica. The crude material was then used as is in Step 4.

Step 4: The title compound was prepared by reacting 4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-5-vinylphenyl)pyridin-2(1H)-one (1.4 g, 3.8 mmol) and N-bromosuccinimide (0.67 g, 3.8 mmol) as described in Example 477 Step 4. Recrystallization from ethyl acetate-hexanes gave the desired product (1.8 g, 99%). ¹H NMR (400 MHz, CDCl₃) δ 7.66 (q, J=8.47 Hz, 1H), 7.46 (dd, J=7.70, 0.77 Hz, 1H), 7.36-7.30 (m, 3H), 7.17 (dt, J=7.71, 2.69, Hz, 1H), 6.72-6.65 (m, 2H), 5.84 (d, J=19.41 Hz, 1H), 5.31 (s, 1H), 5.25 (d, J=10.97 Hz, 1H), 1.91 (s, 3H), 1.88 (s, 3H). ES-HRMS m/z 446.0560 (M+H calcd for C₂₂H₁₉BrF₂NO₂ requires 446.0562).

Example 831

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one

The title compound was prepared by dihydroxylation of the compound from Example 830 (1.0 g, 2.47 mmol) as described in the procedure in Example 478. ¹H NMR (400 MHz, CDCl₃) δ 7.67 (q, J=8.46 Hz, 1H), 7.36-7.30 (m, 3H), 7.17 (ddt, J=8.59, 2.59, 1.10 Hz, 1H), 7.04 (d, J=13.74, 1H), 6.66 (s, 1H), 5.31 (s, 2H), 5.28-5.24 (m, 1H), 4.72-4.60 (m, 1H), 4.56-4.50 (m, 1H), 3.42-3.38 (m, 2H), 1.90 (s, 3H), 1.84, (s 3H). ES-HRMS m/z 480.0611 (M+H calcd for C₂₂H₂₁BrF₂NO₄, requires 480.0617).

Example 832

{1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl Acetate

Step 1: Preparation of (4-hydroxy-2-oxo-2H-pyran-6-yl)methyl Acetate

A slurry of 3-(2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-yl)-2-oxopropyl acetate (Example 653 Step 1) (5 g, 20 mmol) in 30 mL of toluene was heated to reflux under nitrogen environment. LC-MS of the reaction mixture showed 100% conversion to the desired product after 2 h. Heating was stopped and the mixture was allowed to cool to room temperature and stand overnight. The resulting precipitate was filtered and washed with 15 ml of a 1:1 ether/hexane mixture and dried under house vacuum to give desired product (2.95 g, 80%) as off-white solid. ¹H NMR (400 MHz, CDCl₃) δ 10.62 (s, 1H), 6.16 (s, 1H), 5.28 (s, 1H), 4.80 (s, 2H), 2.07 (s, 3H). ES-LCMS m/z 185 (M+H calcd for C₈H₉O₅ requires 185).

Step 2: Synthesis of 1-allyl-4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)methyl Acetate

In a 100 ml round bottom flask the compound from Step 1(1.0 g, 5.45 mmol) and allylamine (0.259 g, 4.54 mmol) were mixed together and dissolved in 27 ml of water. The reaction mixture was heated to reflux under a nitrogen atmosphere for 1.5 h. The reaction was then allowed to cool to room temperature. The solvent was partially concentrated under high vacuum to give a white precipitate. The solid was obtained by filtration through a fritted funnel to yield a (0.625 g, 52% yield) white solid. ¹H NMR (400 MHz, CDCl₃) δ 10.62 (s, 1H), 5.94 (d, J=2.4 Hz, 1H), 5.88-5.78 (m, 1H), 5.58 (d, J=3.0 Hz, 1H), 5.06 (dd, J=10.4, 1.4 Hz, 1H), 4.92(s, 2H), 4.82 (dd, J=17.3, 1.7 Hz, 1H), 4.48-4.46 (m, 1H), 2.06 (s, 3H). ES-LCMS m/z 224 (M+H calcd for C₁₁H₁₄NO₄, requires 224).

Step 3: Preparation of (1-allyl-5-bromo-4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)methyl Acetate

The title compound was prepared by bromination of the product from Step 2 (4.01 g, 18 mmol) as outlined previously in the preparation described in Example 477. The crude product was triturated with diethyl ether to give after filtration the desired product (5.4 g, 99%) as a white solid. ¹H NMR (400 MHz, CDCl₃) δ 11.46 (s, 1H), 6.14 (s, 1H), 5.81-5.91 (m, 1H), 5.09 (dd, J=11.87, 1.75 Hz, 1H), 4.96 (s, 2H), 4.85 (dd, J=18.03, 1.31, 1H), 4.55-4.56 (m, 2H), 2.07 (s, 3H). ES-LCMS m/z 302 (M+H calcd for C₁₁H₁₃BrNO₄, requires 302).

Step 4: Preparation of {1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl Acetate

In a 250 ml round bottom flask 1-allyl-5-bromo-4-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)methyl acetate (5.4 g, 17.94 mmol) was dissolved in 90 mL of DMF. To this reaction was added anhydrous potassium carbonate (2.97 g, 21.52 mmol) followed by addition of 2,4-difluorobenzyl bromide (2.3 ml, 17.94 mmol). The reaction mixture was allowed to stir at room temperature and nitrogen atmosphere for 2.5 h. The reaction was worked up by pouring it into 1 L of ice water. A white fluffy precipitate resulted. The solid was isolated by filtering the reaction mixture through a fritted funnel to give the desired product (7.5 g, 98%) as a white solid. ¹H NMR (400 MHz, CDCl₃) δ 7.62 (q, J=8.33 Hz, 1H), 7.32 (dt, J=9.87, 2.46, Hz, 1H), 7.15 (dt, J=8.3, 2.2, Hz, 1H), 6.64 (s, 1H), 5.90-6.82 (m, 1H), 5.30 (s, 2H), 5.11 (dd, J=10.7, 1.3 Hz, 1H), 5.03 (s, 1H), 4.88 (dd, J=17.3, 1.5, Hz, 1H), 4.60 (d, J=4.8 Hz, 2H), 2.09 (s, 3H). ES-MS m/z 428 (M+H calcd for C₁₈H₁₇BrF₂NO₄ requires 428).

Example 833

1-allyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)pyridin-2(1H)-one

The title compound was prepared by slurrying the above acetate (7.27 g, 17 mmol), Example 832, Step 4 in 100 ml of methanol. To this slurry was added potassium carbonate (4.69 g, 34 mmol). The mixture was allowed to stir at room temperature for 2 h. The reaction was worked up by partially concentrating methanol to approximately 60 ml and cooling the mixture to ˜5° C. in ice bath. Filtration of the reaction gave a white solid, which was washed with water, to give the desired product. (6.3 g, 96% yield). ¹H NMR (400 MHz, CDCl₃) δ 7.62 (q, J=8.1 Hz, 1H), 7.31 (dt, J=10.6, 2.6, Hz, 1H), 7.14 (dt, J=8.8, 2.20, Hz, 1H), 6.57 (s, 1H), 5.92-6.83 (m, 1H), 5.27 (s, 2H), 5.09 (d, J=10.7, Hz, 1H), 4.86 (d, J=6.8, Hz, 1H), 4.63 (s, 2H), 4.24 (s, 2H). ES-HRMS m/z 386.0122 (M+H calcd for C₁₆H₁₅BrF₂NO₃, requires 386.0198).

Example 834

1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl Phenylcarbamate

The title compound was prepared by dissolving 1-allyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)pyridin-2(1H)-one (0.27 g, 0.7 mmol), in a 50 ml round bottom flask, with 2 ml of pyridine. To this mixture was slowly added phenyl isocyanate (0.11 mL, 1 mmol) and the reaction was maintained at room temperature. Within 10 min. the reaction was judged complete by LC-MS analysis. The reaction was poured into ice water (˜25 ml) and diluted with ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate (2×25 ml). The organics were combined, dried, and concentrated in vacuo. The crude product was purified by flash chromatography. Elution with hexanes-ethyl acetate (3:1→0:100) gave the desired product (0.135 g, 39%) as a white crystalline solid. ¹H NMR (400 MHz, CDCl₃) δ 7.60 (q, J=8.1 Hz, 1H), 7.44 (d, J=7.7, 2H), 7.30-7.23 (m, 3H), 7.09 (dt, J=7.74, 2.5 Hz, 1H), 7.00 (t, J=7.7, Hz, 1H), 6.71 (s, 1H), 5.94-5.87 (m, 1H), 5.29 (s, 2H), 5.14-5.11 (m, 3H), 4.91 (d, J=17.0, Hz, 1H), 4.66 (d, J=4.5, Hz, 1H). ES-HRMS m/z 505.0572 (M+H calcd for C₂₃H₂₀BrF₂N₂O₄ requires 505.0569).

Example 835

1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl 2-thien-3-ylethylcarbamate

The title compound was prepared from 1-allyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)pyridin-2(1H)-one (0.27 g, 0.7 mmol) and 3-(2-isocyanato-1-methylethyl)thiophene (0.13 g, 0.84 mmol) as described above in the preparation described in Example 834. ¹H NMR (400 MHz, CDCl₃) δ 7.63-7.60 (m, 1H), 7.30-7.27 (m, 2H), 7.13 (dt, J=8.4, 2.1 Hz, 1H), 6.93-6.28 (m, 2H), 6.60 (s, 1H), 5.94-5.82 (m, 1H), 5.26 (s, 2H), 5.11 (d, J=11.1 Hz, 1H), 4.98 (s, 2H), 4.90 (d, J=17.8 Hz, 1H), 4.60 (dd, J=4.63, 0.9 Hz, 2H), 3.23-3.18 (m, 2H), 2.90 (t, J=7.3 Hz, 2H) 2.85 (t, J=6.8 Hz, 2H). ES-HRMS m/z 539.0454 (M+H calcd for C₂₃H₂₂BrF₂N₂O₄S, requires 539.0446).

Example 836

5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-2-furamide

Step 1: Preparation of the title compound. To a room temperature suspension of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furoic acid (Example 715, step 1) (1.00 g, 2.20 mmol) in THF (20.0 mL) was added 2-chloro-4,6 dimethoxy-1,3,5 triazine (476 mg, 2.70 mmol) and N-methyl morpholine (NMM, 763 mg, 7.28 mmol) sequentially. The resulting solution was matured for 2 h. and then treated with a 2.0 M solution of methylamine (THF, 4.0 mL, 8.0 mmol). The resulting suspension was allowed to continue for 1 additional h. The reaction mixture was diluted with 400 mL of brine and extracted with ethyl acetate (3×400 mL). The organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo and the resulting residue was subjected to a series of washes: 100 mL water (45° C.), 100 mL diethyl ether, 100 mL ethyl acetate/hexanes (1:1). The final remaining solid was the desired compound (591 mg, 54%). ¹H NMR (300 MHz, d₄-MeOH) δ 7.59-7.49 (m, 1H), 7.70-7.69 (m, 3H), 6.45 (s, 2H), 5.33 (s, 2H), 5.20 (s, 2H), 3.60 (s, 3H), 2.61 (s, 3H); LC/MS C-18 column, t_r=2.81 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 467 (M+H). ES-HRMS m/z 467.0415 (M+H calcd for C₂₀H₁₈BrF₂N₂O₄ requires 467.0413).

Example 837

5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)-2-furamide

Step 1: Preparation of the title compound was performed by an identical method as that described for Example 836 by substitution of ethanolamine instead of methylamine. The solid desired title compound was achieved (611 mg, 56%). ES-HRMS m/z 497.0490 (M+H calcd for C₂₁H₂₀BrF₂N₂O₅ requires 497.0518).

Example 838

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[5-(morpholin-4-ylcarbonyl)-2-furyl]methyl}pyridin-2(1H)-one

Step 1: The title compound was made by an identical method as that described in Example 836 but with substitution of 4-morpholine for the methylamine. The solid desired title compound was achieved (506 mg, 44%). ES-HRMS m/z 523.0644 (M+H calcd for C₂₃H₂₂BrF₂N₂O₅ requires 523.0675).

Example 839

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[5-(piperazin-1-ylcarbonyl)-2-furyl]methyl}pyridin-2(1H)-one

Step 1: Preparation of the title compound was completed by an identical method as that described for Example 836 with substitution of 1,4 piperazine instead of methylamine. The solid desired title compound was achieved (348 mg, 30%). ES-HRMS m/z 522.0818 (M+H calcd for C₂₃H₂₃BrF₂N₃O₄ requires 522.0835).

Example 840

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)-2-furyl]methyl}-6-methylpyridin-2(1H)-one

Step 1: Preparation of the title compound. To a room temperature suspension of 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furoic acid (Example 715, Step 1) (600.8 g, 1.32 mmol) in THF (8.0 mL) was added a solution of borane-dimethyl sulfide adduct (THF, 2.0 M, 3.0 mL, 6.0 mmol). The reaction was warmed to 58° C. and maintained for 12 h. The reaction was quenched with a saturated aqueous solution of ammonium chloride (300 mL) and extracted with ethyl acetate (3×200 mL). The organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo and the resulting residue was subjected to normal phase silica chromatography ethyl acetate/hexanes/methanol (57:38:5) to furnish the desired title compound (218 mg, 54%). ¹H NMR (400 MHz, d₄-DMF) δ 7.75 (app q, J=7.3 Hz, 1H), 7.30 (app t, J=8.0 Hz, 1H), 7.19 (app t, J=7.0 Hz, 1H), 6.60 (s, 1H), 6.27 (s, 1H), 6.25 (s, 1H), 5.35 (s, 2H), 5.32 (s, 2H), 5.30 (s, 1H), 4.40 (s, 2H), 2.61 (s, 3H); LC/MS C-18 column, t_r=2.70 min. (5 to 95% acetonitrile/water over 5 min. at 1 m/min with detection 254 nm, at 50° C.). ES-MS m/z 440 (M+H). ES-HRMS m/z 440.0291 (M+H calcd for C₁₉H₁₇BrF₂NO₄ requires 440.0304).

Example 841

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-furyl]-6-methylpyridin-2(1H)-one

Step 1: Preparation of the title compound was done from 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furoic acid (Example 716, Step 3) by an identical method as protocol established for Example 840. The title compound was achieved as a solid (325 mg, 67%). ES-HRMS m/z 426.0104 (M+H calcd for C₁₈H₁₅BrF₂NO₄ requires 426.0147).

Example 842

5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-2-furamide

Step 1: Preparation of the title compound was performed by an identical method as that described for Example 716 with substitution of ethanolamine for ammonium hydroxide. The solid title compound was isolated (591 mg, 54%). ES-HRMS m/z 483.0343 (M+H calcd for C₂₀H₁₈BrF₂N₂O₅ requires 483.0362).

Example 843

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[5-(morpholin-4-ylcarbonyl)-2-furyl]pyridin-2(1H)-one

Step 1: The title compound was prepared by an identical method as that described for Example 716, with substitution of 4-morpholine for ammonium hydroxide. The solid desired title compound was achieved (563 mg, 49%). ES-HRMS m/z 509.0525 (M+H calcd for C₂₂H₂₀BrF₂N₂O₅ requires 509.0518).

Example 844

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[5-(piperidin-1-ylcarbonyl)-2-furyl]pyridin-2(1H)-one

Step 1: The title compound was made by an identical method as that described for Example 716 by substituting piperdine for ammonium hydroxide. The solid desired title compound was achieved (211 mg, 42%). ES-HRMS m/z 507.0707 (M+H calcd for C₂₃H₂₂BrF₂N₂O₄ requires 507.0726).

Example 845

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzoic Acid

Step 1: Preparation of the title compound. To a room temperature solution of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzaldehyde (943 mg, 2.01 mmol) in acetone (10.0 mL) was added 1.5 mL of a 3.0 M solution of Jones Reagent (4.5 mmol). The resulting dark brown solution was stirred for 0.5 h. until complete consumption of starting material was indicated by LC-MS analysis. At this time a gray solid began forming. After an additional 0.5 h., the solid was collected and washed with 10 mL of EtOAc. The resulting solid was the desired product, (787 mg, 81%). Note: the compound showed signs of trace chromium contamination. ¹H NMR (400 MHz, d₄-MeOH) δ 7.80 (br s, 2H), 7.63 (br s, 1H), 7.08 (br s, 2H), 6.70 (br s, 1H), 5.40 (s, 2H), 2.15 (s, 3H); LC/MS C-18 column, t_r=2.60 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 486 (M+H). ES-HRMS m/z 485.9973 (M+H calcd for C₂₀H₁₃BrF₄NO₄ requires 485.9959).

Example 846

4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzamide

Step 1: Preparation of the title compound. To a room temperature solution of 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzoic acid (311.0 mg, 0.637 mol) in THF (6.0 mL) was added 2-chloro-4,6 dimethoxy-1,3,5 triazine (175 mg, 1.00 mmol) and N-methyl morpholine (NMM, 184 mg, 1.82 mmol) sequentially. The resulting solution was matured for 2 h. and then treated with ammonium hydroxide saturated aqueous solution (0.50 ml). The resulting suspension rested for 1 additional hour. The reaction mixture was diluted with 100 mL of brine and extracted with ethyl acetate (3×100 mL). The organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo and the resulting residue was subjected to a series of washes: 20 mL water (45° C.) and 20 mL diethyl ether. The final remaining solid was the desired compound (226 mg, 73%). ¹H NMR (400 MHz, d₄-DMF) δ 7.92 (d, J=8.3 Hz, 2H), 7.80 (app q, J=7.3 Hz, 2H), 7.40 (br s, 1H), 7.35 (dt, J=8.3, 2.4 Hz, 1H), 7.20 (app t, J=7.3 Hz, 1H), 6.80 (s, 1H), 5.49 (s, 2H), 2.20 (s, 3H); LC/MS C-18 column, t_r=2.40 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 485 (M+H). ES-HRMS m/z 485.0098 (M+H calcd for C₂₀H₁₄BrF₄N₂O₃ requires 485.0118).

Example 847

3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(1E)-3-hydroxyprop-1-enyl]phenyl}-6-methylpyridin-2(1H)-one

Step 1: Preparation of the Title Compound

To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-vinylphenyl)-6-methylpyridin-2(1H)-one (489.0 mg, 1.04 mmol) in benzene (10.0 mL) was added, sequentially, (2E)-but-2-ene-1,4-diol (0.298 g, 3.38 mmol) and Grubb's catalyst (trichlorohexylphosphine[1,3 bis-(2,4,6 trimethylphenyl)-4,5-dichlorohydroimidazol-2ylidene]-ruthehenium (IV) dichloride (Sourced by Strem Chemicals, Catalog # 44-777-0) (30.0 mg, 0.0353 mmol). The resulting biphasic mixture was heated to 56° C. and subsequent addition of ruthenium catalyst was made over a 4 h. period of time (25.0 mg, 0.0294 mmol). Complete consumption of starting material, determined by LC-MS analysis, was seen after a total reaction time of 8 h. The reaction was diluted with saturated brine (200 ml) and water (200 mL). This mixture was then extracted with ethyl acetate (3×200 mL) and the organic extracts were separated, Na₂SO₄ dried, and concentrated in vacuo to a volume of approximately 10 mL at which time a solid precipitate formed (310 mg, 60%). ¹H NMR (400 MHz, d₄-MeOH) δ 7.62 (app q, J=8.0 Hz, 1H), 7.30 (d, J=8.8 Hz, 2H), 7.04 (app t, J=9.0 Hz, 2H), 6.70-6.64 (m, 2H), 6.58 (dt, J=16.6, 4.5 Hz, 1H), 5.36 (s, 2H), 4.28 (app d, J=4.6 Hz, 2H), 2.12 (s, 3H); LC/MS C-18 column, t_r=2.87 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 498 (M+H). ES-HRMS m/z 498.0303 (M+H calcd for C₂₂H₁₇BrF₄NO₃ requires 498.0322).

Example 848

(2E)-3-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}prop-2-enyl Carbamate

Step 1: Preparation of the title compound. To a room temperature solution of 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(1E)-3-hydroxyprop-1-enyl]phenyl}-6-methylpyridin-2(1H)-one (189 mg, 0.379 mmol) in CH₂Cl₂ (5.0 mL) was added a solution of trichloroacetyl isocyanate (toluene, 0.53 M, 0.91 mL, 0.48 mmol). The resulting solution was stirred for 1 h. until complete consumption of starting material (LC-MS analysis). The reaction mixture was then directly applied to Al₂O₃ (0.5 g of activity type I) and the slurry was matured for 3 h. At this time, the Al₂O₃ plug was flushed with EtOAc/MeOH (95:5) and the resulting mother liquor was concentrated to a residue that was subjected to SiO₂ chromatography using EtOAc/hexanes/MeOH (6:3.8:0.2) to furnish the title compound as a white solid (190 mg, 94%). ¹H NMR (400 MHz, CDCl₃) δ 7.59 (app q, J=7.9 Hz, 1H), 7.06 (d, J=8.3 Hz, 2H), 6.96 (app dt, J=8.5, 6.0 Hz, 1H), 6.85 (app dt, J=10.0, 3.5 Hz, 1H), 6.55 (d, J=16.0 Hz, 1H), 6.35 (dt, J=16.0, 5.8 Hz, 1H), 6.12 (s, 1H), 5.24 (s, 2H), 4.73 (d, J=6.0, 1.2 Hz, 2H), 2.03 (s, 3H); LC/MS C-18 column, t_r=2.90 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 541 (M+H). ES-HRMS m/z 541.0406 (M+H calcd for C₂₃H₁₈BrF₄N₂O₄ requires 541.0381).

Ecample 849

2-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}-2-hydroxyethyl Carbamate

Step 1: Preparation of the title compound was made from the compound of Example 668 by an identical method as protocol established for Example 848. The solid desired title compound was achieved (283 mg, 74%). ES-HRMS m/z 545.0321 (M+H calcd for C₂₂H₁₈BrF₄N₂O₅ requires 545.0330).

Example 850

1-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}-ethyl 1,2-dicarbamate

Step 1: Preparation of the title compound was made from the compound of Example 668 by an identical method as protocol established for Example 848, substituting 2.5 equivalents of the trichloroacetyl isocyanate. This gave the title compound as a solid (368 mg, 82%). ES-HRMS m/z 588.0356 (M+H calcd for C₂₃H₁₉BrF₄N₃O₆ requires 588.0388).

Example 851

{5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furyl}methyl Carbamate

Step 1: Preparation of the title compound was made from the compound of Example 841 by an identical method as protocol established for Example 848. The solid desired title compound was achieved (211 mg, 75%). ES-HRMS m/z 469.0192 (M+H calcd for C₁₉H₁₆BrF₂N₂O₅ requires 469.0205).

Examle 852

3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)pyridin-2(1H)-one

Step 1: Preparation of the title compound was made from 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione and 6-aminophthalide by the method described in steps 1 and 2 of Example 716, yielding a solid (1.10 g, 53% over two steps). ES-HRMS m/z 462.0149 (M+H calcd for C₂₁H₁₅BrF₂NO₄ requires 462.0147).

Example 853

3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzenesulfonamide

Step 1: Preparation of the title compound was made from 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione and 3-amino-4-methylbenzenesulfonamide by the method described for Example 716 (Steps 1 and 2), giving a solid (689 mg, 30% over two steps). ES-HRMS m/z 499.0134 (M+H calcd for C₂₀H₁₈BrF₂N₂O₄S requires 499.0133).

Example 854

Methyl 5-bromo-2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate

Step 1: Preparation of the title compound was made from 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione and methyl 2-amino-5-bromobenzoate by the method described for Example 716 (Steps 1 and 2), giving a solid (8.10 g, 51% over two steps). ES-HRMS m/z 541.9430 (M+H calcd for C₂₁H₁₆Br₂F₂NO₄ requires 541.9409).

Example 855

Dimethyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalate

Step 1: Preparation of the title compound. At room temperature in a Paar Pressure Bottle (150 psi pressure maximum specification) was added a solution of methyl 5-bromo-2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate (Example 854) (543 g, 1.00 mmol) in anhydrous THF (8 mL) and MeOH (18 mL). Next was added tetrakis(tripheylphosphine)palladium (511 mg, 0.442 mmol) and the pressure bottle was purged with CO gas. The bottle was next pressurized to 60 psi and heated to 61° C. The final pressure of the bottle at this temperature was 72 psi. The reaction mixture was maintained for 36 h. and then vented and cooled. The black solution was concentrated in vacuo and the resulting dark residue was subjected to SiO₂ chromatography with ethyl acetate/hexanes (1:1) to furnish a yellow solid (1.10 g, 63%). ¹H NMR (400 MHz, CDCl₃) δ 8.77 (app d, J=2.3 Hz, 1H), 8.28 (app dd, J=8.3, 2.1 Hz, 1H), 7.43-7.40 (m, 1H), 7.25 (app d, J=9.0 Hz, 1H), 6.93 (app t, J=7.2 Hz, 1H), 6.83 (app t, J=7.4 Hz, 1H), 6.18 (s, 1H), 5.22 (br s, 2H), 3.96 (s, 3H), 3.78 (s, 3H), 1.93 (s, 3H); LC/MS C-18 column, t_r=2.52 min. (5 to 95% acetonitrile/water over 5 min. at 1 ml/min with detection 254 nm, at 50° C.). ES-MS m/z 522 (M+H). ES-HRMS m/z 522.0361 (M+H calcd for C₂₃H₁₉BrF₂NO₆ requires 522.0358).

Example 856

2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylthiophene-3-carboxamide

Step 1: The title compound was made from 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione and 2-amino-4-methyl-thiophene-3-carboxamide by the method described in Example 716 (Steps 1 and 2), giving a solid (612 mg, 27% over two steps). ES-HRMS m/z 469.0036 (M+H calcd for C₁₉H₁₆BrF₂N₂O₃S requires 469.0028).

Example 857

3-bromo-2′-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2H-1,4′-bipyridin-2-one

Step 1: The title compound was made from 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione and 4-amino-2-chloropyridine by the method described for Example 716 (Steps 1 and 2), with a substitution of 18.0 M sulfuric acid instead of methane sulfonic acid, giving a solid (1.67 g, 24% over two steps). ES-HRMS nz/z 440.9790 (M+H calcd for C₁₈H₁₃BrClF₂N₂O₂ requires 440.9811).

Example 858

3-bromo-2′-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2H-1,4′-bipyridin-2-one

Step 1: The title compound was made from 5-(1-hydroxy-3-oxobutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione and 5-amino-2-chloro-3-picoline by the method described for Example 716 (Steps 1 and 2), with a substitution of 18.0 M sulfuric acid instead of methane sulfonic acid, giving a solid (5.56 g, 44% over two steps). ES-HRMS m/z 454.9986 (M+H calcd for C₁₉H₁₅BrClF₂N₂O₂ requires 454.9968).

Example 859

3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

Step 1: Preparation of Methyl 3-[4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

To a cooled (0° C.) solution of methyl 3-[4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate trifluoroacetate (1.03 g, 1.96 mmol) and 1,1-carbonyldiimidazole (0.38 g, 2.4 mmol) in DMA (6.0 mL) was added 4-methylmorpholine (0.32 mL, 3.0 mmol). After 30 min. at ambient temperature, the mixture was cooled (0° C.), cyclobutylamine (0.34 mL, 3.9 mmol) was added, and stirred at room temperature for 3 h. DMA was removed by distillation, and the product was purified by preparatory HPLC using a 10-90% CH₃CN/H₂O (30 min) gradient containing 0.5% TFA at a flow rate of 80 ml/min. Appropriate fractions (M+H m/z=508) were combined and concentrated under reduced pressure to approximately 20 mL. Added 5% NaHCO₃ (20 mL) and extracted with DCM (3×20 mL). The combined organic extracts were dried over Na₂SO₄, filtered, concentrated under reduced pressure, and dried in vacuo to give the desired product as a white foam (0.74 g, 74%). ¹H NMR (CD₃OD/400 MHz) δ 8.03 (d, 1H, J=8.0 Hz), 7.76 (s, 1H), 7.53 (d, 1H, J=8.0 Hz), 7.46 (m, 1H), 7.10 (m, 1H), 7.01 (m, 1H), 6.22 (s, 1H), 6.07 (s, 1H), 5.17 (s, 2H), 4.39 (s, 2H), 4.13 (m, 1H), 3.89 (s, 3H), 2.26 (m, 2H), 2.12 (s, 3H), 1.89 (s, 3H), 1.86 (m, 2H), 1.65 (m, 2H). ESHRMS m/z 508.2262 (M+H calculated for C₂₈H₃₁FN₃O₅ requires 508.2242).

Step 2: Preparation of Methyl 3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

Methyl 3-[4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (from Step 1) (0.60 g, 1.18 mmol) and NCS (0.16 g, 1.18 mmol) were dissolved in acetic acid (10 mL). Dichloroacetic acid (4 drops) was added in a catalytic amount. The mixture was stirred overnight at ambient temperature. Additional NCS (0.02 g, 0.12 mmol) was added and the solution heated at 60° C. for 6.5 h., then stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure and purified by preparatory HPLC using a 10-90% CH₃CN/H₂O (30 min) gradient containing 0.5% TFA at a flow rate of 80 ml/min. Appropriate fractions (M+H m/z=543) were combined and concentrated under reduced pressure to approximately 20 mL. To the fractions was added 5% NaHCO₃ (20 mL), which was then extracted with DCM (3×15 mL). The organic extracts were dried over Na₂SO₄, filtered, concentrated under reduced pressure, and dried in vacuo to give a white solid with one major impurity. The product was further purified by recrystallization from DCM/MeOH using hexane to precipitate the desired product as a white solid (0.33 g, 52%). ¹H NMR (CDCl₃/400 MHz) δ 7.99 (d, 1H, J=8.0 Hz), 7.70 (s, 1H), 7.38 (m, 2H), 7.05 (m, 1H), 6.93 (m, 1H), 6.34 (s, 1H), 5.21 (s, 2H), 4.37 (s, 2H), 4.04 (quintet, 1H, J=8.0 Hz), 3.84 (s, 3H), 2.20 (m, 2H), 2.07 (s, 3H), 1.91 (s, 3H), 1.72 (m, 2H), 1.58 (m, 2H). ESHRMS m/z 542.1851 (M+H calculated for C₂₈H₃₀ClFN₃O₅ requires 542.1853).

Step 3: Preparation of 3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

To methyl 3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (from Step 2) (0.21 g, 0.39 mmol) was added 1.5 N NaOH solution in 1:1 MeOH:water (0.31 mL, 0.46 mmol) and THF (0.41 mL). The reaction mixture was heated with a condenser at 60° C. for 35 min. The solution was cooled (0° C.) and a white solid precipitated by the slow addition of 5% citric acid. Solid was isolated by filtration, washed with H₂O, and dried in vacuo to give the desired product (0.18 g, 87%). ¹H NMR (CD₃OD/400 MHz) δ 8.04 (m, 1H), 7.76 (s, 1H), 7.52 (m, 2H), 7.11 (m, 1H), 7.03 (m, 1H), 6.70 (s, 1H), 5.38 (s, 2H), 4.43 (s, 2H), 4.10 (quintet, 1H, J=8.0 Hz), 2.25 (m, 2H), 2.10 (s, 3H), 2.00 (s, 3H), 1.85 (m, 2H), 1.65 (m, 2H). ESHRMS m/z 528.1730 (M+H calculated for C₂₇H₂₈ClFN₃O₅ requires 528.1696).

Step 4: Preparation of the Title Compound

To a cooled (0° C.) solution of 3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (from Step 3) (0.12 g, 0.23 mmol) in DMA (2.0 mL) was added isobutyl chloroformate (0.35 mL of a stock solution prepared 0.1 mL in 0.9 mL DCM, 0.27 mmol) and 4-methylmorpholine (0.33 mL of a stock solution prepared 0.1 mL in 0.9 mL DMA, 0.30 mmol). The reaction mixture was stirred for 5 min. at 0° C., then for 25 min. at room temperature. The solution was cooled (0° C.), and methylamine (0.17 mL of a 2.0M solution in THF, 0.34 mmol) was added with stirring at ambient temperature for 1.5 h. DMA was removed by distillation under reduced pressure, and the product was purified by preparatory HPLC using a 10-90% CH₃CN/H₂O (30 min.) gradient containing 0.5% TFA at a flow rate of 80 ml/min. Appropriate fractions (M+H m/z=542) were combined, concentrated under reduced pressure, freeze-dried, and lyophilized. The resulting solid was washed with 5% NaHCO₃ (10 mL) and extracted with DCM (3×10 mL). The organic extracts were dried over Na₂SO₄, filtered, concentrated, and dried in vacuo to give the desired product as a white solid (0.06 g, 48%). ¹H NMR (CD₃OD/400 MHz) δ 7.85 (m, 1H), 7.57 (s, 1H), 7.52 (m, 2H), 7.11 (m, 1H), 7.03 (m, 1H), 6.70 (s, 1H), 5.39 (s, 2H), 4.43 (s, 2H), 4.11 (quintet, 1H, J=8.4 Hz), 2.89 (s, 3H), 2.26 (m, 2H), 2.08 (s, 3H), 2.00 (s, 3H), 1.86 (m, 2H), 1.65 (m, 2H). ESHRMS m/z 541.2011 (M+H calculated for C₂₈H₃₁ClFN₄O₄ requires 541.2012).

Example 860

3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

Step 1: Preparation of Methyl 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

Methyl 3-[4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (0.82 g, 1.66 mmol) and NCS (0.22 g, 1.66 mmol) were dissolved in acetic acid (10 mL). Dichloroacetic acid (8 drops) was added in a catalytic amount. The mixture was stirred at ambient temperature overnight. The reaction was not completed by that time, so additional dichloroacetic acid (6 drops) was added and the mixture was again stirred at room temperature overnight. When reaction was still not complete, additional NCS (0.02 g, 0.17 mmol) was added. The reaction was complete 6 h. later, and was concentrated under reduced pressure and purified by preparatory HPLC using a 10-90% CH₃CN/H₂O (30 min) gradient containing 0.5% TFA at a flow rate of 80 ml/min. Appropriate fractions (M+H m/z=528) were combined and concentrated to approximately 20 mL under reduced pressure. Added 5% NaHCO₃ (20 mL) and extracted with DCM (3×15 mL). The organic extracts were dried over Na₂SO₄, filtered, concentrated under reduced pressure, and dried in vacuo to give the desired product as a white foam (0.59 g, 67%). ¹H NMR (CD₃OD/400 MHz) δ 8.04 (m, 1H), 7.79 (s, 1H), 7.54 (m, 2H), 7.14 (m, 1H), 7.03 (m, 1H), 6.72 (s, 1H), 5.41 (s, 2H), 4.48 (s, 2H), 3.89 (s, 3H), 2.47 (m, 1H), 2.10 (s, 3H), 1.99 (s, 3H), 0.69 (m, 2H), 0.46 (m, 2H). ESHRMS m/z 528.1715 (M+H calculated for C₂₇H₂₈ClFN₃O₅ requires 528.1696).

Step 2: Preparation of 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

Preparation was done according to a procedure similar to that used in the synthesis detailed in Step 3 of Example 859. ¹H NMR (DMSO-d₆/400 MHz) δ 7.92 (m, 1H), 7.67 (s, 1H), 7.51 (m, 2H), 7.09 (m, 2H), 6.73 (s, 1H), 5.36 (s, 2H), 4.31 (s, 2H), 2.41 (m, 1H), 2.01 (s, 3H), 1.89 (s, 3H), 0.56 (m, 2H), 0.34 (m, 2H). ESHRMS m/z 514.1537 (M+H calculated for C₂₆H₂₆ClFN₃O₅ requires 514.1540).

Step 3: Preparation of the title compound. The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis detailed in Example 859. ¹H NMR (CD₃OD/400 MHz) δ 7.85 (m, 1H), 7.58 (s, 1H), 7.52 (m, 2H), 7.14 (m, 1H), 7.03 (m, 1H), 6.72 (s, 1H), 5.41 (s, 2H), 4.48 (s, 2H), 2.89 (s, 3H), 2.47 (m, 1H), 2.08 (s, 3H), 2.00 (s, 3H), 0.69 (m, 2H), 0.47 (m, 2H). ESHRMS m/z 527.1865 (M+H calculated for C₂₇H₂₉ClFN₄O₄ requires 527.1856).

Example 861

3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-hydroxy-1-(hydroxymethyl)ethyl]-4-methylbenzamide

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis described in Example 859. ¹H NMR (CD₃OD/400 MHz) δ 7.90 (m, 1H), 7.64 (s, 1H), 7.52 (m, 2H), 7.14 (m, 1H), 7.03 (m, 1H), 6.72 (s, 1H), 5.42 (s, 2H), 4.48 (s, 2H), 4.14 (m, 1H), 3.70 (m, 4H), 2.47 (m, 1H), 2.09 (s, 3H), 2.02 (s, 3H), 0.69 (m, 2H), 0.47 (m, 2H). ESHRMS m/z 587.2083 (M+H calculated for C₂₉H₃₃ClFN₄O₆ requires 587.2067).

Example 862

3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-(dimethylamino)ethyl]-4-methylbenzamide

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis detailed in Example 859. ¹H NMR (CD₃OD/400 MHz) δ 7.88 (m, 1H), 7.63 (s, 1H), 7.52 (m, 2H), 7.14 (m, 1H), 7.03 (m, 1H), 6.72 (s, 1H), 5.42 (s, 2H), 4.48 (s, 2H), 3.51 (t, 2H, J=6.8 Hz), 2.56 (t, 2H, J=6.8 Hz), 2.47 (m, 1H), 2.29 (s, 6H), 2.09 (s, 3H), 2.01 (s, 3H), 0.69 (m, 2H), 0.47 (m, 2H). ESHRMS m/z 584.2437 (M+H calculated for C₃₀H₃₆ClFN₅O₄ requires 584.2434).

Example 863

3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis detailed in Example 859. ¹H NMR (CD₃OD/300 MHz) δ 7.93 (m, 1H), 7.66 (s, 1H), 7.53 (m, 2H), 7.15 (m, 1H), 7.04 (m, 1H), 6.73 (s, 1H), 5.42 (s, 2H), 4.49 (s, 2H), 2.48 (m, 1H), 2.09 (s, 3H), 2.02 (s, 3H), 0.70 (m, 2H), 0.47 (m, 2H). ESHRMS m/z 513.1663 (M+H calculated for C₂₆H₂₇ClFN₄O₄ requires 513.1699).

Example 864

2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluoro-N-(1-methyl-1H-pyrazol-3-yl)benzamide

Step 1: Preparation of Methyl 5-fluoro-2-methylbenzoate

5-fluoro-2-methylbenzoic acid (2.00 g, 13.0 mmol) was combined with 4.0 M hydrogen chloride in 1,4-dioxane (2.5 mL) in MeOH (11 mL) and heated at 70° C. with a condenser overnight. The mixture was concentrated, cooled (0° C.), neutralized with 5% NaHCO₃, extracted with DCM, dried over Na₂SO₄, filtered, concentrated under reduced pressure, and dried in vacuo. The resulting product was obtained as pale yellow oil (1.69 g, 77%). ¹H NMR (CD₃OD/400 MHz) δ 87.55 (d, 1H, J=2.4 Hz), 7.28 (t, 1H, J=6.0 Hz), 7.16 (t, 1H, J=8.4 Hz), 3.87 (s, 3H), 2.51 (s, 3H).

Step 2: Preparation of Methyl 2-(bromomethyl)-5-fluorobenzoate

Methyl-5-fluoro-2-methylbenzoate (Step 1) (1.64 g, 9.75 mmol), NBS (2.08 g, 11.7 mmol), and benzoyl peroxide (0.16 g, 0.68 mmol) in CCl₄ (15 mL) were heated overnight at 80° C. Solid was removed by filtration and subsequently washed with DCM. The filtrate was concentrated and purified by flash column chromatography using hexane and a gradient up to 5% ethyl acetate/hexane as eluent. The resuting product was obtained as colorless liquid (1.79 g, 74%). ¹H NMR (CD₃OD/400 MHz) δ 7.63 (m, 1H), 7.54 (m, 1H), 7.28 (m, 1H), 4.95 (s, 2H), 3.92 (s, 3H).

Step 3: Preparation of Methyl 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzoate

Methyl-2-(bromomethyl)-5-fluorobenzoate (from Step 2) (1.76 g, 7.12 mmol), 3-bromo-1-(2,6-difluorophenyl)-4-hydroxy-6-methylpyridin-2(1H)-one (1.61 g, 5.09 mmol), K₂CO₃ (1.13 g, 8.14 mmol), and 18-crown-6 (0.12 g) were combined in DMA (12 mL) and heated with a condenser at 60° C. After 1 h., DMA was removed by distillation under reduced pressure. The resulting residue was cooled (0° C.), neutralized with 5% citric acid, washed with cold 20% ethyl acetate/hexane, filtered, and dried in vacuo. The product was obtained as a white solid (2.42 g, 99%). ¹H NMR (CD₃OD/400 MHz) δ 7.82 (m, 1H), 7.75 (m, 1H), 7.61 (m, 1H), 7.41 (m, 1H), 7.23 (t, 2H, J=8.4 Hz), 6.61 (s, 1H), 5.68 (s, 2H), 3.91 (s, 3H), 2.10 (s, 3H). ESHRMS m/z 482.0221 and 484.0208 (M+H calculated for C₂₁H₁₆BrF₃NO₄ requires 482.0209 and 484.0192).

Step 4: Preparation of 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzoic Acid

A solution of methyl-2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzoate (from Step 3) (1.88 g, 3.90 mmol) and 2.0 N NaOH (2.9 mL) in dioxane (2.9 mL) was heated at 55° C. for 1.5 h. The reaction mixture was cooled (0° C.), neutralized with 5% citric acid, washed with water, and the product was obtained by filtration as a white solid (1.60 g, 88%). ¹H NMR (CD₃OD/400 MHz) δ 7.79 (m, 1H), 7.69 (m, 1H), 7.60 (m, 1H), 7.34 (m, 1H), 7.23 (t, 2H, J=8.8 Hz), 6.62 (s, 1H), 5.70 (s, 2H), 2.08 (s, 3H). ESHRMS r/z 468.0061 and 470.0052 (M+H calculated for C₂₀H₁₄BrF₃NO₄ requires 468.0053 and 470.0035).

Step 5: Preparation of the title compound. To a cooled (0° C.) solution of 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzoic acid (from Step 4) (0.22 g, 0.47 mmol) in DMA (2.0 mL) was added isobutyl chloroformate (0.73 mL of a stock solution prepared 0.1 mL in 0.9 mL DCM, 0.56 mmol) and 4-methylmorpholine (0.67 mL of a stock solution prepared 0.1 mL in 0.9 mL DMA, 0.61 mmol). The mixture was stirred for 5 min. at 0° C. then for 25 min. at ambient temperature. The reaction was cooled (0° C.) and 1-methyl-1H-pyrazol-3-amine (0.07 g, 0.70 mmol) was added. The mixture was stirred at room temperature for 1.5 h., and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by preparatory HPLC using a 10-90% CH₃CN/H₂O (30 min.) gradient containing 0.5% TFA at a flow rate of 80 mL/min. Appropriate fractions (M+H m/z=548) were combined, concentrated under reduced pressure, freeze-dried, and lyophilized. The resulting solid was washed with 5% NaHCO₃ (10 mL), extracted in DCM (3×10 mL), dried over Na₂SO₄, filtered, concentrated under reduced pressure, and dried in vacuo to give the desired product as a peach-colored solid (0.15 g, 58%). ¹H NMR (CD₃OD/300 MHz) δ 7.79 (m, 1H), 7.64 (m, 1H), 7.50 (m, 2H), 7.38 (m, 1H), 7.27 (t, 2H, J=7.8 Hz), 6.68 (s, 1H), 6.60 (s, 1H), 5.61 (s, 2H), 3.85 (s, 3H), 2.11 (s, 3H). ESHRMS m/z 547.0560 and 549.0530 (M+H calculated for C₂₄H₁₉BrF₃N₄O₃ requires 547.0587 and 549.0570).

Example 865

2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzamide

The title compound was prepared using a procedure similar to that used in Step 5 of the synthesis described in Example 864. ¹H NMR (CD₃OD/300 MHz) δ 7.72 (m, 1H), 7.60 (m, 1H), 7.38 (m, 1H), 7.29 (m, 1H), 7.23 (t, 2H, J=7.6 Hz), 6.64 (s, 1H), 5.54 (s, 2H), 2.08 (s, 3H). ESHRMS m/z 467.0199 and 469.0176 (M+H calculated for C₂₀H₁₅BrF₃N₂O₃ requires 467.0213 and 469.0195).

Example 866

2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-N—(Cyclopropylmethyl)-5-fluorobenzamide

The title compound was prepared using a procedure similar to that used in Step 5 of the synthesis detailed in Example 864. ¹H NMR (CD₃OD/400 MHz) 87.68 (m, 1H), 7.60 (m, 1H), 7.29 (m, 2H), 7.23 (t, 2H, J=8.4 Hz), 6.64 (s, 1H), 5.49 (s, 2H), 3.19 (d, 2H, J=7.2 Hz), 2.09 (s, 3H), 1.04 (m, 1H), 0.49 (m, 2H), 0.24 (m, 2H). ESHRMS m/z 521.0693 and 523.0676 (M+H calculated for C₂₄H₂₁BrF₃N₂O₃ requires 521.0682 and 523.0665).

Example 867

3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

Step 1: Preparation of Methyl 3-[4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

To a cooled (0° C.) solution of methyl 3-[4-{[2-(aminomethyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate trifluoroacetate (1.94 g, 3.7 mmol) and 1,1-carbonyldiimidazole (0.72 g, 4.4 mmol) in DMA (23 mL) was added 4-methylmorpholine (0.61 mL, 5.5 mmol). The mixture was stirred at room temperature for 30 min., cooled (0° C.), and ethylamine (3.7 mL of a 2.0 M solution in THF, 7.4 mmol) added. Solution was stirred for 2 h. at ambient temperature, and solvent was removed by distillation under reduced pressure. Residue was purified by preparatory HPLC using a 10-90% CH₃CN/H₂O (30 min.) gradient containing 0.5% TFA at a flow rate of 80 ml/min. Appropriate fractions (M+H m/z=482) were combined and concentrated under reduced pressure to approximately 30 mL. Added 5% NaHCO₃ (30 mL) and extracted with DCM (3×15 mL). The organic extracts were dried over Na₂SO₄, filtered, concentrated under reduced pressure, and dried in vacuo to give the desired product as a gummy, pale yellow solid in quantitative yield. ¹H NMR (CD₃OD/400 MHz) 88.03 (m, 1H), 7.76 (s, 1H), 7.53 (d, 1H, J=8.0 Hz), 7.45 (m, 1H), 7.11 (m, 1H), 7.01 (m, 1H), 6.22 (s, 1H), 6.07 (s, 1H), 5.18 (s, 2H), 4.40 (s, 2H), 3.89 (s, 3H), 3.15 (q, 2H, J=7.2 Hz), 2.11 (s, 3H), 1.89 (s, 3H), 1.09 (t, 3H, J=7.2 Hz). ESHRMS m/z 482.2049 (M+H calculated for C₂₆H₂₉FN₃O₅ requires 482.2086).

Step 2: Preparation of Methyl 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

NBS (0.77 g, 4.3 mmol) was added portionwise to a solution of methyl 3-[4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]4-methylbenzoate (from Step 1) (2.08 g, 4.3 mmol) in DCM (25 mL). The solution was stirred at room temperature for 30 min., washed with water (20 mL), extracted in DCM (2×10 mL), dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The resulting yellow foam was purified by filtration from a cooled (0° C.) solution in ethyl acetate and was washed with a cold solution of 30% ethyl acetate in hexane to give the desired product as an off-white solid (1.51 g, 63%). ¹H NMR (CD₃OD/400 MHz) δ 8.04 (m, 1H), 7.78 (s, 1H), 7.54 (m, 2H), 7.13 (m, 1H), 7.03 (m, 1H), 6.67 (s, 1H), 5.39 (s, 2H), 4.46 (s, 2H), 3.89 (s, 3H), 3.13 (q, 2H, J=7.2 Hz), 2.10 (s, 3H), 1.98 (s, 3H), 1.09 (t, 3H, J=7.2 Hz). ESHRMS m/z 560.1223 and 562.1183 (M+H calculated for C₂₆H₂₈FBrN₃O₅ requires 560.1191 and 562.1175).

Step 3: Preparation of 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

To methyl 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate (from Step 2) (1.47 g, 2.6 mmol) was added 1.5 N NaOH solution in 1:1 MeOH:H₂O (2.6 mL, 3.9 mmol) and THF (3.6 mL). The mixture was heated at 60° C. with a condenser for 1 h. White solid was precipitated from the cooled (0° C.) solution by the slow addition of 5% citric acid, filtered, and dried in vacuo to give the product as a pale yellow solid (1.40 g, 99%). ¹H NMR (CD₃OD/400 MHz) 68.04 (d, 1H, J=9.6 Hz), 7.76 (s, 1H), 7.54 (m, 1H), 7.13 (m, 1H), 7.03 (m, 1H), 6.67 (s, 1H), 5.39 (s, 2H), 4.46 (s, 2H), 3.14 (q, 2H, J=7.2 Hz), 2.09 (s, 3H), 1.99 (s, 3H), 1.09 (t, 3H, J=6.8 Hz). ESHRMS m/z 546.1060 and 548.1049 (M+H calculated for C₂₅H₂₆BrFN₃O₅ requires 546.1034 and 548.1018).

Step 4: Preparation of the Title Compound

To a cooled (0° C.) solution of 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid (from Step 3) (0.22 g, 0.40 mmol) in DMA (2 mL) was added isobutyl chloroformate (0.63 mL of a stock solution prepared 0.1 mL in 0.9 mL DCM, 0.56 mmol) and 4-methylmorpholine (0.58 mL of a stock solution prepared 0.1 mL in 0.9 mL DMA, 0.61 mmol). The mixture was stirred for 5 min. at 0° C. then for 25 min. at ambient temperature. The solution was cooled (0° C.), methylamine (0.30 mL, 0.60 mmol) was added as a 2.0 M solution in THF, and the mixture was stirred at room temperature for 2.5 h. DMA was removed by distillation under reduced pressure and the resulting residue was purified by preparatory HPLC using a 10-90% CH₃CN/H₂O (30 min.) gradient containing 0.5% TFA at a flow rate of 80 ml/min. Appropriate fractions (M+H m/z=560) were combined and concentrated under reduced pressure to approximately 20 mL. Added 5% NaHCO₃ (10 mL) and extracted in DCM (3×10 mL). The organic extracts were dried over Na₂SO₄, filtered, concentrated under reduced pressure, and dried in vacuo to give the desired product as a white solid (0.12 g, 54%). ¹H NMR (CD₃OD/400 MHz) δ 7.85 (m, 1H), 7.54 (m, 3H), 7.12 (m, 1H), 7.02 (m, 1H), 6.67 (s, 1H), 5.40 (s, 2H), 4.45 (s, 2H), 3.14 (q, 2H, J=7.2 Hz), 2.89 (s, 3H), 2.08 (s, 3H), 1.99 (s, 3H), 1.09 (t, 3H, J=6.8 Hz). ESHRMS m/z 559.1353 and 561.1324 (M+H calculated for C₂₆H₂₉BrFN₄O₄ requires 559.1351 and 561.1334).

Example 868

3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis described in Example 867. ¹H NMR (CD₃OD/400 MHz) δ 7.91 (m, 1H), 7.64 (s, 1H), 7.53 (m, 2H), 7.13 (m, 1H), 7.03 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.45 (s, 2H), 3.14 (q, 2H, J=7.2 Hz), 2.09 (s, 3H), 2.00 (s, 3H), 1.09 (t, 3H, J=7.2 Hz). ESHRMS nz/z 545.1183 and 547.1198 (M+H calculated for C₂₅H₂₇BrFN₄O₄ requires 545.1194 and 547.1178).

Example 869

3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-(dimethylamino)ethyl]-4-methylbenzamide

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis in Example 867. ¹H NMR (CD₃OD/400 MHz) 87.88 (m, 1H), 7.62 (s, 1H), 7.53 (m, 2H), 7.12 (m, 1H), 7.03 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.45 (s, 2H), 3.51 (t, 2H, J=5.6 Hz), 3.14 (q, 2H, J=7.2 Hz), 2.56 (t, 2H, J=6.8 Hz), 2.30 (s, 6H), 2.08 (s, 3H), 2.00 (s, 3H), 1.09 (t, 3H, J=7.2 Hz). ESHRMS m/z 616.1933 and 618.1900 (M+H calculated for C₂₉H₃₆BrFN₅O₄ requires 616.1929 and 618.1914).

Example 870

N-(2-{[(3-bromo-1-{5-[(2,2-dimethylhydrazino)carbonyl]-2-methylphenyl}-6-methyl-2-oxo-1,2-dihydropyridin-4-yl)oxy]methyl}-5-fluorobenzyl)-N′-ethylurea

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis described in Example 867. ¹H NMR (CD₃OD/400 MHz) δ 7.82 (m, 1H), 7.53 (m, 3H), 7.13 (m, 1H), 7.03 (m, 1H), 6.68 (s, 1H), 5.40 (s, 2H), 4.45 (s, 2H), 3.14 (q, 2H, J=7.6 Hz), 2.62 (s, 6H), 2.08 (s, 3H), 2.00 (s, 3H), 1.09 (t, 3H, J=7.2 Hz). ESHRMS m/z 588.1663 and 590.1605 (M+H calculated for C₂₇H₃₂BrFN₅O₄ requires 588.1616 and 590.1600).

Example 871

3-[3-bromo-4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide

Step 1: Preparation of Methyl 3-[4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

Prepared using a procedure similar to that used in Step 1 of the synthesis described in Example 867. ¹H NMR (CD₃OD/400 MHz) δ 8.03 (m, 1H), 7.77 (s, 1H), 7.53 (d, 1H, J=8.0 Hz), 7.47 (m, 1H), 7.13 (m, 1H), 7.02 (m, 1H), 6.22 (s, 1H), 6.09 (s, 1H), 5.21 (s, 2H), 4.47 (s, 2H), 3.89 (s, 3H), 3.67 (s, 3H), 2.11 (s, 3H), 1.89 (s, 3H). ESHRMS m/z 484.1888 (M+H calculated for C₂₅H₂₇FN₃O₆ requires 484.1878).

Step 2: Preparation of Methyl 3-[3-bromo-4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate

This compound was prepared using a procedure similar to that used in Step 2 of the synthesis described in Example 867. ¹H NMR (CD₃OD/400 MHz) δ 8.04 (m, 1H), 7.78 (s, 1H), 7.55 (m, 2H), 7.16 (m, 1H), 7.04 (m, 1H), 6.68 (s, 1H), 5.43 (s, 2H), 4.52 (s, 2H), 3.89 (s, 3H), 3.67 (s, 3H), 2.09 (s, 3H), 1.97 (s, 3H). ESHRMS m/z 562.0971 and 564.0980 (M+H calculated for C₂₅H₂₆BrFN₃O₆ requires 562.0984 and 564.0967).

Step 3: Preparation of 3-[3-bromo-4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic Acid

This compound was prepared using a procedure similar to that used in Step 3 of the synthesis described in Example 867. ¹H NMR (CD₃OD/400 MHz) δ 8.03 (m, 1H), 7.75 (s, 1H), 7.53 (m, 2H), 7.16 (m, 1H), 7.04 (m, 1H), 6.67 (s, 1H), 5.43 (s, 2H), 4.53 (s, 2H), 3.67 (s, 3H), 2.09 (s, 3H), 1.98 (s, 3H). ESHRMS m/z 548.0830 and 548.0827 (M+H calculated for C₂₄H₂₄BrFN₃O₆ requires 548.0827 and 550.0810).

Step 4: Preparation of the Title Compound

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis described in Example 867. ¹H NMR (CD₃OD/400 MHz) δ 7.85 (m, 1H), 7.54 (m, 3H), 7.15 (m, 1H), 7.04 (m, 1H), 6.68 (s, 1H), 5.43 (s, 2H), 4.52 (s, 2H), 3.67 (s, 3H), 2.89 (s, 3H), 2.08 (s, 3H), 1.99 (s, 3H). ESHRMS m/z 561.1126 and 563.1108 (M+H calculated for C₂₅H₂₇BrFN₄O₅ requires 561.1143 and 563.1127).

Example 872

3-[3-bromo-4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide

The title compound was prepared using a procedure similar to that used in Step 4 of the synthesis described in Example 867. ¹H NMR (CD₃OD/400 MHz) δ 7.91 (m, 1H), 7.64 (s, 1H), 7.53 (m, 2H), 7.15 (m, 1H), 7.04 (m, 1H), 6.68 (s, 1H), 5.44 (s, 2H), 4.52 (s, 2H), 3.67 (s, 3H), 2.08 (s, 3H), 1.99 (s, 3H). ESHRMS m/z 547.0959 and 549.0950 (M+H calculated for C₂₄H₂₅BrFN₄O₅ requires 547.0987 and 549.0970).

Example 873

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(2,6-dimethyl-3H-benzoimidazol-5-yl)-6-methyl-pyridin-2(1H)-one

Step 1. Preparation of 4-(2,4-difluorobenzyloxy)-1-(2,6-dimethyl-3H-benzoimidazol-5-yl)-6-methyl-pyridin-2(1H)-one

1-(2,6-Dimethyl-3H-benzoimidazol-5-yl)-4-hydroxy-6-methyl-pyridin-2(1H)-one (El Kihel, A. et al. Synthetic. Commun. 1999, 29, 2435-2445) (1.4 g, 5.2 mmol) and DBU (0.8 mL, 5.5 mmol) was dissolved in 10 mL of NMP and 2,4-difluorobenzyl bromide (0.7 mL, 5.5 mmol) was added. The reaction was stirred at 80° C. for 12 h. The reaction was cooled room temperature, diluted with water, and extracted 3 times with EtOAc. The combined organics were washed with brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 89:10:1 CHCl₃/MeOH/concentrated ammonium hydroxide) provided a tan solid (0.54 g, 25%): ¹H NMR (300 MHz, DMSO-d₆) δ 12.47 (s, 1H), 7.86 (app q, J=8.5 Hz, 1H), 7.60-7.51 (m, 2H), 7.41-7.34 (m, 2H), 6.25 (d, J=2.3 Hz, 1H), 6.16 (d, J=2.6 Hz, 1H), 5.31 (s, 2H), 2.62 (s, 3H), 2.19 (s, 3H), 1.97 (s, 3H).

Step 2. Preparation of title compound. 4-(2,4-Difluorobenzyloxy)-1-(2,6-dimethyl-3H-benzoimidazol-5-yl)-6-methyl-pyridin-2(1H)-one (0.53 g, 1.3 mmol) and NCS (0.2 g, 1.5 mmol) were dissolved in 7 mL DMF, and the reaction was stirred at room temperature for 18 h. The reaction was diluted with water, and extracted 3 times with EtOAc. The combined organics were washed with brine, dried (MgSO₄), filtered and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 89:10:1 CHCl₃/MeOH/concentrated ammonium hydroxide) gave an off-white solid (0.06 g, 10%): ¹H NMR (300 MHz, DMSO-d₆) δ 12.14 (br s, 1H), 7.70 (d, J=6.7 Hz, 1H), 7.44-7.34 (m, 2H), 7.30 (s, 1H), 7.21 (d, J=1.8 Hz, 1H), 6.73 (s, 1H), 5.34 (s, 2H), 2.50 (s, 3H), 1.95 (s, 3H), 1.89 (s, 3H). ES-HRMS m/z 430.1126 (M+H calcd for C₂₂H₁₉ClF₂N₃O₂ requires 430.1128).

Example 874

2-{5-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]-1H-indol-3-yl}-N,N-dimethyl-2-oxo-acetamide

Step 1. Preparation of the title compound. 3-Chloro-4-(2,4-difluorobenzyloxy)-1-(1H-indol-5-ylmethyl)-pyridin-2(1H)-one (0.3 g, 0.75 mmol) was dissolved in 4 mL of CH₂Cl₂ at 0° C. and oxalyl chloride (0.07 mL, 0.82 mmol) was added dropwise. After 30 min. the solvent was evaporated on a rotary evaporator and the residue was suspended in 4 mL THF. To this suspension was added a solution of dimethylamine (0.94 mL of a 2.0 M solution in THF, 1.9 mmol). The reaction was stirred at room temperature for 12 h. The reaction was partitioned between water and ethyl acetate, and separated. The organic layer was washed with brine, dried (MgSO₄), filtered and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 84:15:1 CHCl₃/MeOH/concentrated ammonium hydroxide) gave an off-white solid (0.05 g, 13%): ¹H NMR (300 MHz, DMSO-d₆) δ 12.32 (br s, 1H), 8.10 (d, J=6.4 Hz, 1H), 7.99 (d, J=7.8 Hz, 1H), 7.49 (d, J=8.4 Hz, 1H), 7.36-7.26 (m, 2H), 7.15 (app t, J=6.3 Hz, 1H), 6.62 (d, J=7.9 Hz, 1H), 5.30 (s, 2H), 5.25 (s, 2H), 2.98 (s, 3H), 2.86 (s, 3H). ES-HRMS m/z 500.1213 (M+H calcd for C₂₅H₂₁ClF₂N₃O₄ requires 500.1183).

Example 875

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(3-dimethylaminomethyl-1H-indol-5-ylmethyl)-pyridin-2(1H)-one

Step 1. Preparation of the title compound. A suspension of paraformaldehyde (0.03 mg, 0.85 mmol), acetic acid (0.05 mL, 0.85 mmol), and a solution of dimethylamine (0.43 mL of a 2.0 M in THF, 0.85 mmol) in 3 mL of EtOH was stirred at 80° C. until a homogeneous solution formed. The reaction was cooled to room temperature, a solution of 3-Chloro-4-(2,4-difluorobenzyloxy)-1-(1H-indol-5-ylmethyl)-pyridin-2(1H)-one from Example 874, Step 1(0.3 g, 0.75 mmol) in 3.0 mL EtOH was added, and the resulting reaction mixture was stirred at 80° C. for 18 h. The reaction was cooled to room temperature and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 84:15:1 CHCl₃/MeOH/concentrated ammonium hydroxide) gave a white solid (0.14 g, 41%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.98 (s, 1H), 7.90 (d, J=7.8 Hz, 1H), 7.62-7.57 (m, 2H), 7.36-7.23 (m, 3H), 7.15 (app t, J=8.5 Hz, 1H), 7.06 (dd, J=8.4, 1.5 Hz, 1H), 6.57 (d, J=7.8 Hz, 1H), 5.28 (s, 2H), 5.18 (s, 2H), 3.54 (s, 2H), 2.16 (s, 6H). ES-HRMS m/z 458.1430 (M+H calcd for C₂₄H₂₃ClF₂N₃O₂ requires 458.1441).

Example 876

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(3-pyrrolidin-1-ylmethyl-1H-indol-5-ylmethyl)-pyridin-2(1H)-one

Step 1. The title compound was prepared by a procedure similar to the one described for Example 875 (0.24 g, 66%): ¹H NMR (300 MHz, DMSO-d₆) δ 11.24 (br s, 1H), 7.91 (d, J=9 Hz, 1H), 7.63-7.60 (m, 2H), 7.32-7.05 (m, 5H), 6.57 (d, J=8 Hz, 1H), 5.23 (s, 2H), 5.18 (s, 2H), 3.78 (s, 2H), 2.50 (s, 4H), 1.69 (s, 1H). ES-HRMS m/z 484.1595 (M+H calcd for C₂₆H₂₅ClF₂N₃O₂ requires 454.1598).

Example 877

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(2,3-dihydro-1H-isoindol-5-ylmethyl)-pyridin-2(1H)-one Trifluoroacetic Acid Salt

Step 1. Preparation of 1,3-dihydroisoindole-2,5-dicarboxylic Acid 5-methyl Ester 2-(2,2,2-trichloroethyl) Ester

2,3-Dihydro-1H-isoindole-5-carboxylic acid methyl ester (3.0 g, 17 mmol) and triethylamine (3.5 mL, 25 mmol) dissolved in 60 mL of THF was cooled to 0° C. The reaction mixture was treated with 2,2,2-trichloroethyl chloroformate (3.4 mL, 25 mmol). The reaction mixture was warm to room temperature and stirred for 1.5 h. The precipitate was filtered and the filtrate was diluted with EtOAc. The organics were washed with a solution of 10% citric acid, brine, dried (Na₂SO₄), filtered and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:4 EtOAc/hexanes) afforded a light tan solid (5.74 g, 97%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.98 (s, 1H), 7.92 (d, J=8 Hz, 1H), 7.52 (t, J=7 Hz, 1H), 4.92 (s, 2H), 4.83 (s, 2H), 4.76 (s, 2H), 3.86 (s, 3H).

Step 2. Preparation of 5-hydroxymethyl-1,3-dihydroisoindole-2-carboxylic Acid 2,2,2-trichloroethyl Ester

1,3-Dihydroisoindole-2,5-dicarboxylic acid 5-methyl ester 2-(2,2,2-trichloroethyl) ester (7.3 g, 21 mmol) was dissolved in 70 mL of THF, cooled to −78° C., and DIBAL (67.3 mL of a 1.0 M solution in toluene, 67.3 mmol) was added dropwise. The reaction continued to stir at −78° C. for 5 h. The reaction mixture was warmed to room temperature and quenched with a 1:1 solution of 10% citric acid in water/methanol, and evaporated on a rotary evaporator. The residue was dissolved in EtOAc, washed 3 times with Rochelle salt, brine, dried (Na₂SO₄), filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:1 EtOAc/Hexanes) gave a light yellow solid (3.90 g, 58%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.30-7.25 (m, 3H), 5.24-5.20 (m, 1H), 5.06 (s, 2H), 4.91 (s, 2H), 4.75 (s, 2H), 4.68 (s, 2H).

Step 3. Preparation of 5-bromomethyl-1,3-dihydroisoindole-2-carboxylic Acid 2,2,2-trichloroethyl Ester

5-Hydroxymethyl-1,3-dihydroisoindole-2-carboxylic acid 2,2,2-trichloroethyl ester (2.0 g, 6.2 mmol), was dissolved in 25 mL of CH₂Cl₂, followed by treatment of triphenylphosphine and carbon tetrabromide. The reaction was stirred at room temperature for 30 min. The solvent was evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 1:1 EtOAc/Hexanes) provided a viscous orange oil, which was carried forwarded without further characterization.

Step 4. Preparation of 5-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]-1,3-dihydroisoindole-2-carboxylic Acid 2,2,2-trichloroethyl Ester

3-Chloro-4-(2,4-difluoro-benzyloxy)-pyridin-2(1H)-one (1.1 g, 4.8 mmol) and potassium carbonate (1.3 g, 9.5 mmol) were dissolved in 40 mL of DMF, followed by treatment of 5-bromomethyl-1,3-dihydroisoindole-2-carboxylic acid 2,2,2-trichloroethyl ester (2.2 g, 5.7 mmol). The reaction was stirred at 80° C. for 21 h. The reaction was cooled to room temperature, diluted with brine and extracted 3 times with EtOAc. The combined organics were washed with water, brine, dried (Na₂SO₄), filtered, and evaporated on a rotary evaporator. Purification by flash column chromatography (silica; CH₂Cl₂) afforded an off-white solid, (1.1 g, 38%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.96-7.92 (, 1H), 7.63 (app q, J=8 Hz, 1H), 7.37-7.28 (m, 4H), 7.16 (app t, J=6 Hz, 1H), 6.62 (d, J=8 Hz, 1H), 5.30 (s, 2H), 5.14 (s, 2H), 4.90 (s, 2H), 4.74 (s, 2H), 4.67 (s, 2H).

Step 5. Preparation of title compound. To solution of zinc dust (0.6 g, 9.1 mmol) in a 5 mL solution of NH₄OAc (1.0 M in water) was added a solution of 5-[3-chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]-1,3-dihydroisoindole-2-carboxylic acid 2,2,2-trichloroethyl ester (1.1 g, 1.8 mmol) in 25 mL of THF. The reaction mixture stirred at room temperature for 4.5 hr. The solution was adjusted to pH 8 using a saturated solution of NaHCO₃, and extracted 3 times with CH₂Cl₂. The combined organics were washed with brine, dried (Na₂SO₄), filtered and evaporated on a rotary evaporator. Purification by preparatory HPLC (Phenomenex Luna 10μ, C18(2) 250×21.2 mm) provided an off-white solid (0.08 g, 11%): ¹H NMR (300 MHz, DMSO-d₆) δ 9.30 (br s, 1H), 7.96 (d, J=8 Hz, 1H), 7.63 (app q, J=9 Hz, 1H), 7.39-7.30 (m, 4H), 7.16 (app t, J=2 Hz, 1H), 6.64 (d, J=8 Hz, 1H), 5.30 (s, 2H), 5.15 (s, 2H), 4.47 (br s, 4H). ES-HRMS m/z 403.1004 (M+H calcd for C₂₁H₁₈ClF₂N₂O₂ requires 403.1019).

Example 878

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(3-morpholin-4-ylmethyl-1H-indol-5-ylmethyl)-pyridin-2(1H)-one

Step 1. The title compound was prepared by a procedure similar to the one described for Example 875 (0.16 g, 43%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.97 (br s, 1H), 7.91 (d, J=8 Hz, 1H), 7.63-7.57 (m, 2H), 7.37-7.05 (m, 5H), 6.58 (d, J=8 Hz, 1H), 5.28 (s, 2H), 5.19 (s, 2H), 3.58-3.53 (m, 6H), 2.33 (br s, 4H). ES-HRMS m/z 500.1443 (M+H calcd for C₂₆H₂₅ClF₂N₃O₃ requires 500.1547).

Example 879

3-Chloro-4-(2,4-difluoro-benzyloxy)-1-(3-piperidin-1-ylmethyl-1H-indol-5-ylmethyl)-pyridin-2(1H)-one

Step 1. The title compound was prepared by a procedure similar to the one described for Example 875 (0.18 g, 48%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.92 (br s, 1H), 7.90 (d, J=8 Hz, 1H), 7.62-7.57 (m, 2H), 7.37-7.27 (m, 2H), 7.18-7.12 (m, 2H), 7.05 (d, J=8 Hz, 1H), 6.58 (d, J=8 Hz, 1H), 5.28 (s, 2H), 5.18 (s, 2H), 3.53 (s, 2H), 2.30 (br s, 4H), 1.43-1.35 (m, 6H). ES-HRMS m/z 498.1727 (M+H calcd for C₂₇H₂₇ClF₂N₃O₂ requires 498.1754).

Example 880

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(3-methylaminomethyl-1H-indol-5-ylmethyl)-pyridin-2(1H)-one

Step 1. The title compound was prepared by a procedure similar to the one described for Example 875 (0.06 g, 18%): ¹H NMR (300 MHz, DMSO-d₆) δ 11.05 (s, 1H), 7.90 (d, J=7.7 Hz, 1H), 7.67-7.57 (m, 2H), 7.37-7.29 (m, 3H), 7.17-7.07 (m, 2H), 6.57 (d, J=7.8 Hz, 1H), 5.40 (br s, 1H), 5.28 (s, 2H), 5.18 (s, 2H), 3.91 (s, 2H), 2.38 (s, 3H). ES-HRMS m/z 444.1266 (M+H calcd for C₂₃H₂₁ClF₂N₃O₂ requires 444.1285).

Example 881

3-[3-Bromo-4-(2,4-difluorophenoxymethyl)-6-methyl-2-oxo-pyridin-1(2H)-yl]-4,N-dimethyl Benzamide

Step 1. Preparation of 1-(5-methoxycarbonyl-2-methylphenyl)-6-methyl-2-oxo-1,2-dihydropyridine-4-carboxylic Acid

6-Methyl-2-oxo-2H-pyran-4-carboxylic acid (Hasizume, K. et al. Chem. Pharm. Bull. 1968, 16, 2292-2296) (3.4 g, 22 mmol) and 3-amino-4-methyl-benzoic acid methyl ester (3.6 g, 22 mmol) were suspended 110 mL of 1-butanol, and stirred at 120° C. for 24 h. The reaction was cooled room temperature, and the solvent was evaporated on a rotary evaporator. The residue was diluted with a saturated solution of NaHCO₃, and washed 3 times with EtOAc. The aqueous layer was acidified to pH 3 the concentrated HCl, and extracted 3 times with EtOAc. The combined organics were washed with brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator to provide a white solid (2.1 g, 32%): ¹H NMR (300 MHz, DMSO-d₆) δ 14.01 (br s, 1H), 7.98 (dd, J=7.9, 1.6 Hz, 1H), 7.76 (d, J=1.4 Hz, 1H), 7.60 (d, J=7.9, 1H), 6.84 (s, 1H), 6.67 (s, 1H), 3.85 (s, 3H), 2.04 (s, 3H), 1.90 (s, 3H).

Step 2. Preparation of 3-(4-hydroxymethyl-6-methyl-2-oxo-pyridin-1(2H)-yl)-4-methyl Benzoic Acid Methyl Ester

1-(5-Methoxycarbonyl-2-methylphenyl)-6-methyl-2-oxo-1,2-dihydropyridine-4-carboxylic acid (2.1 g, 7.0 mmol) and triethylamine (1.5 mL, 10 mmol) were dissolved in 20 mL of THF, and cooled to 0° C. To this reaction mixture was added ethyl chloroformate (1.0 mL, 10 mmol). After 1 h. the solid was filtered, the filtrate was cooled to 0° C., sodium borohydride (0.26 g, 7.0 mmol) was added, and 20 mL of water was added dropwise. The reaction was warmed to room temperatures stirred for 3 h. The reaction solvent was evaporated on a rotary evaporator to provide a light yellow oil (1.6 g, 80%): ¹H NMR (300 MHz, CDCl₃) δ 8.02 (dd, J=7.9, 1.7 Hz, 1H), 7.77 (d, J=1.6 Hz, 1H), 7.45 (d, J=7.9 Hz, 1H), 6.55 (s, 1H), 6.18 (s, 1H), 4.51 (d, J=5.0 Hz, 2H), 3.89 (s, 3H), 2.14 (s, 3H), 1.88 (s, 3H).

Step 3. Preparation of 3-(4-bromomethyl-6-methyl-2-oxo-pyridin-1(2H)-yl)-4-methyl Benzoic Acid Methyl Ester

3-(4-Hydroxymethyl-6-methyl-2-oxo-pyridin-1(2H)-yl)-4-methyl benzoic acid methyl ester (1.6 g, 5.6 mmol), triphenylphosphine (1.8 g, 6.7 mmol), and carbon tetrabromide (2.2 g, 6.7 mmol) were dissolved in 20 mL of methylene chloride, and stirred for 30 min. The solvent was evaporated on a rotary evaporator. Purification by flash column chromatography (silica; EtOAc) provided a light yellow solid (0.3 g, 16%): ¹H NMR (300 MHz, CDCl₃) δ 8.05 (dd, J=8.0, 1.7 Hz, 1H), 7.79 (d, J=1.7 Hz, 1H), 7.45 (d, J=8.0, 1H), 6.54 (d, J=1.0 Hz, 1H), 6.20 (d, J=1.0 Hz, 1H), 4.23 (s, 2H), 3.89 (s, 3H), 2.15 (s, 3H), 1.90 (s, 3H).

Step 4. Preparation of 3-[4-(2,4-difluorophenoxymethyl)-6-methyl-2-oxo-pyridin-1(2H)-yl]4-methyl Benzoic Acid Methyl Ester

3-(4-Bromomethyl-6-methyl-2-oxo-pyridin-1(2H)-yl)-4-methyl benzoic acid methyl ester (0.3 g, 0.86 mmol), cesium carbonate (0.56 g, 1.7 mmol), and 2,4-difluorophenol (0.1 mL, 1.0 mmol) were dissolved in 10 mL of dioxane, and stirred at 105° C. for 12 h. The reaction was cooled room temperature, diluted with EtOAc, washed with water, brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator to provide a light yellow oil (0.27 g, 80%): ¹H NMR (300 MHz, CDCl₃) δ 8.04 (dd, J=8.0, 1.7 Hz, 1H), 7.79 (d, J=1.7 Hz, 1H), 7.45 (d, J=8.0, 1H), 6.96-6.80 (m, 3H), 6.62 (s, 1H), 6.28 (s, 1H), 4.95 (s, 2H), 3.89 (s, 3H), 2.15 (s, 3H), 1.92 (s, 3H).

Step 5. Preparation of 3-[3-bromo-4-(2,4-difluorophenoxymethyl)-6-methyl-2-oxo-pyridin-1(2H)-yl]-4-methyl Benzoic Acid Methyl Ester

3-[4-(2,4-Difluorophenoxymethyl)-6-methyl-2-oxo-pyridin-1(2H)-yl]-4-methyl benzoic acid methyl ester (0.27 g, 0.68 mmol) was dissolved in 3 mL of acetic acid, cooled to 0° C., and a solution of bromine (0.04 mL, 0.72 mmol) in 1 mL of acetic acid was added dropwise. The reaction was warmed to room temperature, and stirred for 2 h. The solvent was evaporated on a rotary evaporator to provide a yellow oil (0.32 g, 100%): ¹H NMR (300 MHz, CDCl₃) δ 8.06 (dd, J=6.6, 1.3 Hz, 1H), 7.75 (d, J=1.1 Hz, 1H), 7.47 (d, J=7.9, 1H), 7.13-7.08 (m, 1H), 6.94-6.81 (m, 2H), 6.62 (s, 1H), 5.39 (s, 2H), 3.90 (s, 3H), 2.16 (s, 3H), 2.15 (s, 3H).

Step 6. Preparation of 3-[3-bromo-4-(2,4-difluorophenoxymethyl)-6-methyl-2-oxo-pyridin-1(2H)-yl]-4-methyl Benzoic Acid

3-[3-Bromo-4-(2,4-difluorophenoxymethyl)-6-methyl-2-oxo-pyridin-1(2H)-yl]-4-methyl-benzoic acid methyl ester (0.32 g, 0.68 mmol) was dissolved in 2.0 mL of MeOH, and a solution of KOH (2.0 mL of a 1.0 M solution in water, 2.0 mmol). After 3 h. the solvent was evaporated on a rotary evaporator. The residue was dissolved in water and washed 2 times with diethyl ether. The aqueous layer was acidified to pH 3 with 1 N HCl, and extracted 3 times with 3:1 CHCl₃/isopropanol. The combined organics were washed with brine, dried (MgSO₄), filtered, and evaporated on a rotary evaporator to provide a off-white solid (0.27 g, 87%): ¹H NMR (300 MHz, CDCl₃) δ 8.10 (dd, J=7.9, 1.4 Hz, 1H), 7.80 (d, J=1.4 Hz, 1H), 7.50 (d, J=7.9, 1H), 7.13-7.08 (m, 1H), 6.95-6.90 (m, 1H), 6.88-6.81 (m, 1H), 6.62 (s, 1H), 5.40 (s, 2H), 2.16 (s, 3H), 2.15 (s, 3H).

Step 7. The title compound was prepared by a procedure similar to the one described for Example 656 (0.02 g, 7%): ¹H NMR (300 MHz, DMSO-d₆) δ 7.76-7.43 (m, 3H), 6.97-6.81 (m, 4H), 6.39 (br s, 1H), 5.01 (s, 2H), 2.91 (s, 3H), 2.13 (s, 3H), 2.11 (s, 3H).). ES-HRMS m/z 477.0610 (M+H calcd for C₂₂H₂₀BrF₂N₂O₃ requires 477.0620).

Example 882

3-Chloro-4-(2,4-difluorobenzyloxy)-1-(3-piperazin-1-ylmethyl-1H-indol-5-yl-methyl)-pyridin-2(1H)-one dihydrochloride salt

Step 1. Preparation of 4-{5-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-ylmethyl]-1H-indol-3-yl-methyl}-piperazine-1-carboxylic Acid Tert-Butyl Ester

A suspension of paraformaldehyde (0.03 mg, 0.85 mmol), acetic acid (0.05 mL, 0.85 mmol), and tert-Butyl 1-piperazine-carboxylate (0.16, 0.85 mmol) in 3 mL of EtOH was stirred at 80° C. until a homogeneous solution formed. The reaction was cooled to room temperature, a solution of the compound from Example 874 (0.3 g, 0.75 mmol) in 3.0 mL EtOH was added, and the resulting reaction mixture was stirred at 80° C. for 18 h. The reaction was cooled to room temperature and evaporated on a rotary evaporator. Purification by flash column chromatography (silica, 90:10 CHCl₃/MeOH) gave an off-white solid (0.17 g, 38%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.97 (s, 1H), 7.91 (d, J=8 Hz, 1H) 7.63-7.57 (m, 2H), 7.35-7.04 (m, 5H), 6.58 (d, J=8 Hz, 1H), 5.28 (s, 2H), 5.18 (s, 2H), 3.60 (s, 2H), 3.26 (br s, 4H), 2.29 (br s, 4H), 1.36 (s, 9H).

Step 2. Preparation of title compound. 4-{5-[3-Chloro-4-(2,4-difluorobenzyloxy)-2-oxo-pyridin-1(2H)-yl-methyl]-1H-indol-3-ylmethyl}-piperazine-1-carboxylic acid tert-butyl ester (0.17 g, 0.28 mmol) was diluted with a solution of HCl (4 mL of a 4.0 M solution in dioxane, 1.0 mmol) and the reaction was stirred at room temperature for 2 h. The solvent was evaporated on a rotary evaporator to afford a tan solid (0.15 g, 99%): ¹H NMR (300 MHz, DMSO-d₆) δ 11.62 (br s, 2H), 9.57 br s, 1H), 9.21 (br s, 1H), 7.96-7.91 (m, 2H) 7.69-7.60 (m, 2H), 7.43-7.31 (m, 2H), 7.19-7.12 (m, 2H), 6.57 (d, J=8 Hz, 1H), 5.29 (s, 2H), 5.20 (s, 2H), 4.54 (br s, 2H), 3.70-3.30 (m, 7H). ES-HRMS m/z 499.1718 (M+H calcd for C₂₆H₂₆ClF₂N₄O₂ requires 499.1707).

Example 883

3-Chloro-4-(2,4-difluorobenzyloxy)-1-{3-[(2-hydroxyethylamino)methyl]-1H-indol-5-ylmethyl}-pyridin-2(1H)-one

Step 1. The title compound was prepared by a procedure similar to the one described for Example 875 (0.04 g, 13%): ¹H NMR (300 MHz, DMSO-d₆) δ 11.05 (br s, 2H), 7.90 (d, J=7.7 Hz, 1H), 7.68-7.57 (m, 2H), 7.37-7.29 (m, 3H) 7.16 (app t, J=8.7 Hz, 1H), 7.09 (d, J=8.5 Hz, 1H), 6.57 (d, J=7.8 Hz, 1H), 5.28 (s, 2H), 5.19 (s, 2H), 4.65 (br s, 1H), 3.97 (s, 2H), 3.53 (br s, 2H), 2.73 (t, J=5.5 Hz, 2H). ES-HRMS nz/z 474.1418 (M+H calcd for C₂₄H₂₃ClF₂N₃O₃ requires 474.1391).

Example 884

3-Chloro-4-(2,4-difluorobenzyloxy)-1-{3-[(2-dimethylaminoethylamino)methyl]-1H-indol-5-ylmethyl}-pyridin-2(1H)-one

Step 1. The title compound was prepared by a procedure similar to the one described for Example 875 (0.11 g, 29%): ¹H NMR (300 MHz, DMSO-d₆) δ 10.98 (s, 1H), 7.89 (d, J=8 Hz, 1H), 7.63-7.57 (m, 2H), 7.36-7.29 (m, 3H), 7.18-7.07 (m, 2H), 6.56 (d, J=8 Hz, 1H), 5.28 (s, 2H), 5.18 (s, 2H), 3.90 (s, 2H), 3.39 (br s, 1H), 2.68 (t, J=6 Hz, 2H), 2.34 (t, J=6 Hz, 2H), 2.10 (s, 6H). ES-HRMS m/z 501.1870 (M+H calcd for C₂₆H₁₈ClF₂N₄O₂ requires 501.1863).

Biological Evaluation

p38 Kinase Assay

Cloning of Human p38a:

The coding region of the human p38a cDNA was obtained by PCR-amplification from RNA isolated from the human monocyte cell line THP.1. First strand CDNA was synthesized from total RNA as follows: 2 μg of RNA was annealed to 100 ng of random hexamer primers in a 10 μl reaction by heating to 70° C. for 10 minutes followed by 2 minutes on ice. cDNA was then synthesized by adding 1 μl of RNAsin (Promega, Madison Wis.), 2 μl of 50 mM dNTP's, 4 μl of 5× buffer, 2 μl of 100 mM DTT and 1 μl (200 U) of Superscript II™ AMV reverse transcriptase. Random primer, dNTP's and Superscript II™ reagents were all purchased from Life-Technologies, Gaithersburg, Mass. The reaction was incubated at 42° C. for 1 hour. Amplification of p38 cDNA was performed by aliquoting 5 μl of the reverse transcriptase reaction into a 100 μl PCR reaction containing the following: 80 μl dH.sub.2 O, 2. μl 50 mM dNTP's, 1 μl each of forward and reverse primers (50 pmol/μl), 10 μl of 10× buffer and 1 μl Expand™ polymerase (Boehringer Mannheim). The PCR primers incorporated Bam HI sites onto the 5′ and 3′ end of the amplified fragment, and were purchased from Genosys. The sequences of the forward and reverse primers were 5′-GATCGAGGATTCATGTCTCAGGAGAGGCCCA-3′ and 5′GATCGAGGATTCTCAGGACTCCATCTCTTC-3′ respectively. The PCR amplification was carried out in a DNA Thermal Cycler (Perkin Elmer) by repeating 30 cycles of 94° C. for 1 minute, 60° C. for 1 minute and 68° C. for 2 minutes. After amplification, excess primers and unincorporated dNTP's were removed from the amplified fragment with a Wizard™ PCR prep (Promega) and digested with Bam HI (New England Biolabs). The Bam HI digested fragment was ligated into BamHI digested pGEX 2T plasmid DNA (PharmaciaBiotech) using T-4 DNA ligase (New England Biolabs) as described by T. Maniatis, Molecular Cloning: A Laboratory Manual, 2nd ed. (1989). The ligation reaction was transformed into chemically competent E. coli DH10B cells purchased from Life-Technologies following the manufacturer's instructions. Plasmid DNA was isolated from the resulting bacterial colonies using a Promega Wizard™ miniprep kit. Plasmids containing the appropriate Bam HI fragment were sequenced in a DNA Thermal Cycler (Perkin Elmer) with Prism™ (Applied Biosystems Inc.). cDNA clones were identified that coded for both human p38a isoforms (Lee et al. Nature 372, 739). One of the clones that contained the cDNA for p38a-2 (CSB-2) inserted in the cloning site of PGEX 2T, 3′ of the GST coding region was designated pMON 35802. The sequence obtained for this clone is an exact match of the cDNA clone reported by Lee et al. This expression plasmid allows for the production of a GST-p38a fusion protein.

Expression of Human p38a

GST/p38a fusion protein w as expressed from the plasmid pMON 35802 in E. coli, stain DH10B (Life Technologies, Gibco-BRL). Overnight cultures were grown in Luria Broth (LB) containing 100 mg/ml ampicillin. The next day, 500 ml of fresh LB was inoculated with 10 ml of overnight culture, and grown in a 2 liter flask at 37° C. with constant shaking until the culture reached an absorbance of 0.8 at 600 nm. Expression of the fusion protein was induced by addition of isopropyl b-D-thiogalactosidase (IPTG) to a final concentration of 0.05 mM. The cultures were shaken for three hours at room temperature, and the cells were harvested by centrifugation. The cell pellets were stored frozen until protein purification.

Purification of P38 Kinase-Alpha

All chemicals were from Sigma Chemical Co. unless noted. Twenty grams of E. coli cell pellet collected from five 1 L shake flask fermentations was resuspended in a volume of PBS (140 mM NaCl, 2.7 mM KCl, 10 mM Na.sub.2 HPO.sub.4, 1.8 mM KH.sub.2 PO.sub.4, pH 7.3) up to 200 ml. The cell suspension was adjusted to 5 mM DTT with 2 M DTT and then split equally into five 50 ml Falcon conical tubes. The cells were sonnicated (Ultrasonics model W375) with a 1 cm probe for 3.times.1 minutes (pulsed) on ice. Lysed cell material was removed by centrifugation (12,000×g, 15 minutes) and the clarified supernatant applied to glutathione-sepharose resin (Pharmacia).

Glutathione-Sepharose Affinity Chromatography

Twelve ml of a 50% glutathione sepharose-PBS suspension was added to 200 ml clarified supernatant and incubated batchwise for 30 minutes at room temperature. The resin was collected by centrifugation (600.times.g, 5 min) and washed with 2.times.150 ml PBS/1% Triton X-100, followed by 4.times.40 ml PBS. To cleave the p38 kinase from the GST-p38 fusion protein, the glutathione-sepharose resin was resuspended in 6 ml PBS containing 250 units thrombin protease (Pharmacia, specific activity>7500 units/mg) and mixed gently for 4 hours at room temperature. The glutathione-sepharose resin was removed by centrifugation (600.times.g, 5 min) and washed 2.times.6 ml with PBS. The PBS wash fractions and digest supernatant containing p38 kinase protein were pooled and adjusted to 0.3 mM PMSF.

Mono Q Anion Exchange Chromatography

The thrombin-cleaved p38 kinase was further purified by FPLC-anion exchange chromatography. Thrombin-cleaved sample was diluted 2-fold with Buffer A (25 mM HEPES, pH 7.5, 25 mM beta-glycerophosphate, 2 mM DTT, 5% glycerol) and injected onto a Mono Q HR 10/10 (Pharmacia) anion exchange column equilibrated with Buffer A. The column was eluted with a 160 ml 0.1 M-0.6 M NaCl/Buffer A gradient (2 ml/minute flowrate). The p38 kinase peak eluting at 200 mM NaCl was collected and concentrated to 3-4 ml with a Filtron 10 concentrator (Filtron Corp.).

Sephacryl S100 Gel Filtration Chromatography

The concentrated Mono Q-p38 kinase purified sample was purified by gel filtration chromatography (Pharmacia HiPrep 26/60 Sephacryl S100 column equilibrated with Buffer B (50 mM HEPES, pH 7.5, 50 mM NaCl, 2 mM DTT, 5% glycerol)). Protein was eluted from the column with Buffer B at a 0.5 ml/minute flowrate and protein was detected by absorbance at 280 nm. Fractions containing p38 kinase (detected by SDS-polyacrylamide gel electrophoresis) were pooled and frozen at −80° C. Typical purified protein yields from 5 L E. coli shake flasks fermentations were 35 mg p38 kinase.

In Vitro Assay

The ability of compounds to inhibit human p38 kinase alpha was evaluated using two in vitro assay methods. In the first method, activated human p38 kinase alpha phosphorylates a biotinylated substrate, PHAS-I (phosphorylated heat and acid stable protein-insulin inducible), in the presence of gamma ³²P-ATP (³²P-ATP). PHAS-I was biotinylated prior to the assay and provides a means of capturing the substrate, which is phosphorylated during the assay. p38 Kinase was activated by MKK6. Compounds were tested in 10 fold serial dilutions over the range of 100 μM to 0.001 μM using 1% DMSO. Each concentration of inhibitor was tested in triplicate.

All reactions were carried out in 96 well polypropylene plates. Each reaction well contained 25 mM HEPES pH 7.5, 10 mM magnesium acetate and 50 μM unlabeled ATP. Activation of p38 was required to achieve sufficient signal in the assay. Biotinylated PHAS-I was used at 1-2 μg per 50 μl reaction volume, with a final concentration of 1.5 μM. Activated human p38 kinase alpha was used at 1 μg per 50 μl reaction volume representing a final concentration of 0.3 μM. Gamma ³²P-ATP was used to follow the phosphorylation of PHAS-I. ³²P-ATP has a specific activity of 3000 Ci/mmol and was used at 1.2 μCi per 50 μl reaction volume. The reaction proceeded either for one hour or overnight at 30° C.

Following incubation, 20 μl of reaction mixture was transferred to a high capacity streptavidin coated filter plate (SAM-streptavidin-matrix, Promega) prewetted with phosphate buffered saline. The transferred reaction mix was allowed to contact the streptavidin membrane of the Promega plate for 1-2 minutes. Following capture of biotinylated PHAS-I with ³²p incorporated, each well was washed to remove unincorporated ³²P-ATP three times with 2M NaCl, three washes of 2M NaCl with 1% phosphoric, three washes of distilled water and finally a single wash of 95% ethanol. Filter plates were air-dried and 20 μl of scintillant was added. The plates were sealed and counted.

A second assay format was also employed that is based on p38 kinase alpha induced phosphorylation of EGFRP (epidermal growth factor receptor peptide, a 21 mer) in the presence 33P-ATP. Compounds were tested in 10 fold serial dilutions over the range of 100 μM to 0.001 μM in 1% DMSO. Each concentration of inhibitor was tested in triplicate. Compounds were evaluated in 50 μl reaction volumes in the presence of 25 mM Hepes pH 7.5, 10 mM magnesium acetate, 4% glycerol, 0.4% bovine serum albumin, 0.4 mM DTT, 50 μM unlabeled ATP, 25 μg EGFRP (200 μM), and 0.05 μCi ³³P-ATP. Reactions were initiated by addition of 0.09 μg of activated, purified human GST-p38 kinase alpha. Activation was carried out using GST-MKK6 (5:1, p38:MKK6) for one hour at 30° C. in the presence of 50 μM ATP. Following incubation for 60 minutes at room temperature, the reaction was stopped by addition of 150 μl of AG 1.times.8 resin in 900 mM sodium formate buffer, pH 3.0 (1 volume resin to 2 volumes buffer). The mixture was mixed three times with pipetting and the resin was allowed to settle. A total of 50 μl of clarified solution head volume was transferred from the reaction wells to Microlite-2 plates. 150 μl of Microscint 40 was then added to each well of the Microlite plate, and the plate was sealed, mixed, and counted.

Representative compounds that exibit IC₅₀ values between 1 and 25 μM (p38 alpha kinase assay) are: Example Nos. 20, 22, 23, 39, 43, 44, 48, 50, 52, 53, 55, 57, 58, 62, 92, 115, 118, 136, 139, 141, 142, 149, 156, 157, 169, 174, 219, 220, 244, 245, 387, 288, 289, 291, 292, 293, 294, 295, 296, 298, 297, 300, 301, 302 304, 305, 309, 310, 311, 323, 360, 394, 403, 414, 415, 416, 418, 420, 444, 447, 449, 451, 452, 471, 485, 486, 496, 498, 499, 503, 506, 561, 569, 574, 575, 576, 738, 812, and 837.

Representatve compounds that exibit IC₅₀ values between 25 and 100 μM (p38 alpha kinase assay) are: Example Nos. 1, 25, 33, 35, 37, 42, 45, 47, 49, 119, 204, 308, 558, 560, 564, 565, 566, 568, 577, and 865.

Representatve compounds that exibit IC₅₀ values less than 1 μM (p38 alpha kinase assay) are: Example Nos. 6, 14, 8, 17, 10, 15, 4, 117, 161, 162, 165, 170, 171, 172, 173 176, 179, 217, 218, 219, 220, 221, 223, 225, 230, 231, 234, 235, 272, 273, 275, 276, 278, 280, 282, 286, 285, 290, 312, 313, 314, 315, 316, 317, 318, 320, 321, 322, 364, 366, 400, 402, 405, 421, 422, 423, 446, 448, 450, 458, 466, 467, 468, 469, 470, 481, 482, 483, 484, 487, 489, 492, 493, 494, 495, 504, 521, 522, 523, 557, 587, 589, 590, 591, 597, 609, 610, 613, 629, 642, 643, 736, 757, 777, 785, 804, 807, 815, 838, 847, 849, and 863.

Representatve compounds that exibit IC₅₀ values greater than 100 μM (p38 alpha kinase assay) are: Example Nos. 3, 11, 38, 56, 116, 121, 237, 236, 413, 497 and 578.

TNF Cell Assays

Method of Isolation of Human Peripheral Blood Mononuclear Cells:

Human whole blood was collected in Vacutainer tubes containing EDTA as an anticoagulant. A blood sample (7 ml) was carefully layered over 5 ml PMN Cell Isolation Medium (Robbins Scientific) in a 15 ml round bottom centrifuge tube. The sample was centrifuged at 450-500.times.g for 30-35 minutes in a swing out rotor at room temperature. After centrifugation, the top band of cells were removed and washed 3 times with PBS w/o calcium or magnesium. The cells were centrifuged at 400.times.g for 10 minutes at room temperature. The cells were resuspended in Macrophage Serum Free Medium (Gibco BRL) at a concentration of 2 million cells/mi.

LPS Stimulation of Human PBMs

PBM cells (0.1 ml, 2 million/ml) were co-incubated with 0.1 ml compound (10-0.41 μM, final concentration) for 1 hour in flat bottom 96 well microtiter plates. Compounds were dissolved in DMSO initially and diluted in TCM for a final concentration of 0.1% DMSO. LPS (Calbiochem, 20 ng/ml, final concentration) was then added at a volume of 0.010 ml. Cultures were incubated overnight at 37° C. Supernatants were then removed and tested by ELISA for TNF-a and IL1-b. Viability was analyzed using MTS. After 0.1 ml supernatant was collected, 0.020 ml MTS was added to remaining 0.1 ml cells. The cells were incubated at 37° C. for 2-4 hours, then the O.D. was measured at 490-650 nM.

Maintenance and Differentiation of the U937 Human Histiocytic Lymphoma Cell Line

U937 cells (ATCC) were propagated in RPMI 1640 containing 10% fetal bovine serum, 100 IU/ml penicillin, 100 μg/ml streptomycin, and 2 mM glutamine (Gibco). Fifty million cells in 100 ml media were induced to terminal monocytic differentiation by 24 hour incubation with 20 ng/ml phorbol 12-myristate 13-acetate (Sigma). The cells were washed by centrifugation (200.times.g for 5 min) and resuspended in 100 ml fresh medium. After 24-48 hours, the cells were harvested, centrifuged, and resuspended in culture medium at 2 million cells/ml.

LPS Stimulation of TNF Production by U937 Cells

U937 cells (0.1 ml, 2 million/ml) were incubated with 0.1 ml compound (0.004-50 μM, final concentration) for 1 hour in 96 well microtiter plates. Compounds were prepared as 10 mM stock solutions in DMSO and diluted in culture medium to yield a final DMSO concentration of 0.1% in the cell assay. LPS (E coli, 100 ng/ml final concentration) was then added at a volume of 0.02 ml. After 4 hour incubation at 37° C., the amount of TNF-.alpha. released in the culture medium was quantitated by ELISA. Inhibitory potency is expressed as IC50 (μM).

Rat Assay

The efficacy of the novel compounds in blocking the production of TNF also was evaluated using a model based on rats challenged with LPS. Male Harlen Lewis rats [Sprague Dawley Co.] were used in this model. Each rat weighed approximately 300 g and was fasted overnight prior to testing. Compound administration was typically by oral gavage (although intraperitoneal, subcutaneous and intravenous administration were also used in a few instances) 1 to 24 hours prior to the LPS challenge. Rats were administered 30 μg/kg LPS [salmonella typhosa, Sigma Co.] intravenously via the tail vein. Blood was collected via heart puncture 1 hour after the LPS challenge. Serum samples were stored at −20° C. until quantitative analysis of TNF-.alpha. by Enzyme Linked-Immuno-Sorbent Assay (“ELISA”) [Biosource]. Additional details of the assay are set forth in Perretti, M., et al., Br. J. Pharmacol. (1993), 110, 868-874, which is incorporated by reference in this application.

Mouse Assay

Mouse Model of LPS-Induced TNF Alpha Production

TNF alpha was induced in 10-12 week old BALB/c female mice by tail vein injection with 100 ng lipopolysaccharide (from S. Typhosa) in 0.2 ml saline. One hour later mice were bled from the retroorbital sinus and TNF concentrations in serum from clotted blood were quantified by ELISA. Typically, peak levels of serum TNF ranged from 2-6 ng/ml one hour after LPS injection.

The compounds tested were administered to fasted mice by oral gavage as a suspension in 0.2 ml of 0.5% methylcellulose and 0.025% Tween 20 in water at 1 hour or 6 hours prior to LPS injection. The 1 hour protocol allowed evaluation of compound potency at Cmax plasma levels whereas the 6 hour protocol allowed estimation of compound duration of action. Efficacy was determined at each time point as percent inhibition of serum TNF levels relative to LPS injected mice that received vehicle only.

Induction and Assessment of Collagen-Induced Arthritis in Mice

Arthritis was induced in mice according to the procedure set forth in J. M. Stuart, Collagen Autoimmune Arthritis, Annual Rev. Immunol. 2:199 (1984), which is incorporated herein by reference. Specifically, arthritis was induced in 8-12 week old DBA/1 male mice by injection of 50 μg of chick type II collagen (CII) (provided by Dr. Marie Griffiths, Univ. of Utah, Salt Lake City, Utah) in complete Freund's adjuvant (Sigma) on day 0 at the base of the tail. Injection volume was 100 μl. Animals were boosted on day 21 with 50 μg of CII in incomplete Freund's adjuvant (100 μl volume). Animals were evaluated several times each week for signs of arthritis. Any animal with paw redness or swelling was counted as arthritic. Scoring of arthritic paws was conducted in accordance with the procedure set forth in Wooley et al., Genetic Control of Type II Collagen Induced Arthritis in Mice: Factors Influencing Disease Suspectibility and Evidence for Multiple MHC Associated Gene Control., Trans. Proc., 15:180 (1983). Scoring of severity was carried out using a score of 1-3 for each paw (maximal score of 12/mouse). Animals displaying any redness or swelling of digits or the paw were scored as 1. Gross swelling of the whole paw or deformity was scored as 2. Ankylosis of joints was scored as 3. Animals were evaluated for 8 weeks. 8-10 animals per group were used.

The invention and the manner and process of making and using it, are now described in such full, clear, concise and exact terms as to enable any person skilled in the art to which it pertains, to make and use the same. It is to be understood that the foregoing describes preferred embodiments of the present invention and that modifications may be made therein without departing from the spirit or scope of the present invention as set forth in the claims. To particularly point out and distinctly claim the subject matter regarded as invention, the following claims conclude this specification.

Claims

1. A compound or a pharmaceutically acceptable salt thereof, wherein: the compound corresponds in structure to the following formula: R1 is H, halogen, NO2, alkyl, carboxaldehyde, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkenyl, alkynyl, arylalkynyl, —CN, aryl, alkanoyl, alkoxy, alkoxyalkyl, haloalkyl, haloalkoxy, carboxyl, or arylalkanoyl, wherein: the aryl portion of arylalkoxy, arylalkyl, and arylalkanoyl is unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently halogen, C1-C4 alkyl, C1-C4 alkoxy, nitro, CN, haloalkyl, haloalkoxy or CO2R; the alkyl portion of the alkyl, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, arylalkyl, alkanoyl, alkoxy, alkoxyalkyl and arylalkanoyl is unsubstituted or substituted with 1, 2, or 3 substituents that are independently halogen, C1-C4 alkoxy, C1-C4 alkoxycarbonyl, or C3-C7 cycloalkyl; R2 is H, OH, halogen, —OSO2—(C1-C6)alkyl, —OSO2-aryl, arylalkoxy, aryloxy, arylthio, arylthioalkoxy, arylalkynyl, alkoxy, aryloxy(C1-C6)alkyl, alkyl, alkynyl, —OC(O)NH(CH2)naryl, —OC(O)N(alkyl)(CH2)naryl, alkoxyalkoxy, dialkylamino, alkyl, alkoxy, aryl, arylalkyl, heteroaryl, heteroarylalkyl, arylalkenyl, heterocycloalkyl, heterocycloalkylalkyl, alkoxyalkoxy, NR8R9, dialkylamino, or CO2R, wherein: each such substituent is unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently halogen, —(C1-C6)alkyl-N(R)—CO2R30, —(C1-C4 alkyl)-NR6C(O)NR7—(C1-C6 alkoxy), —(C1-C4 alkyl)-NR16C(O)NR17—(C3-C6 cycloalkyl), —(C1-C4 alkyl)-NR16C(O)NR17—(C3-C6 cycloalkylalkyl), —(C1-C4 alkyl)-NR16C(O)NR17-(heteroaryl) wherein the heteroaryl is optionally substituted with C1-C4 alkyl, C1-C4 alkoxy, halogen or OH, haloalkyl, heteroaryl, heteroarylalkyl, —NR6R7, R6R7N—(C1-C6 alkyl)-, —(C1-C4 alkyl)-NR6(CO)NR7—(C1-C6 alkoxy), —C(O)NR6R7, —(C1-C4)alkyl-C(O)NR6R7, —(C1-C4 alkyl)-NRC(O)NR16R17, haloalkoxy, alkyl, CN, hydroxyalkyl, dihydroxyalkyl, alkoxy, alkoxycarbonyl, phenyl, —SO2-phenyl wherein the phenyl and —SO2-phenyl substituents are optionally substituted with 1, 2, or 3 substituents that are independently halogen or NO2, or —OC(O)NR6R7; n is 0, 1, 2, 3, 4, 5 or 6; as to R16 and R17: R16 and R17 are independently H, C1-C6 alkyl, or C1-C6 alkoxy; or R16, R17, and the nitrogen to which they are attached form a morpholinyl ring; as to R6 and R7: R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or heteroaryl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR16R17, alkanoyl, arylalkyl, arylalkoxy, —NR16SO2-alkyl, —NR16SO2-phenyl, alkoxycarbonyl, —SO2-alkyl, —SO2-aryl, OH, alkoxy, alkoxyalkyl, arylalkoxycarbonyl, —(C1-C4)alkyl-CO2-alkyl, phenyl, heteroarylalkyl, heterocycloalkyloxy, alkenyl optionally substituted with —OC(O)NR6R7, aryl, heterocycloalkylalkanoyl, or arylalkanoyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, alkoxy, heterocycloalkyl, heterocycloalkylalkyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy, or R6, R7, and the nitrogen to which they are attached form a morpholinyl, pyrrolidinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dionyl, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, alkoxycarbonyl, C1-C4 alkoxy, hydroxyl, hydroxyalkyl, dihydroxyalkyl, or halogen; R at each occurrence is independently hydrogen or C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl; R30 is C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl; each R8 is independently hydrogen, alkyl, alkanoyl, arylalkyl and arylalkanoyl, wherein: each such substituent is optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl; each R9 is hydrogen, alkyl, alkanoyl, arylalkyl, cycloalkyl, cycloalkylalkyl, alkenyl, heteroaryl, aminoalkyl, monoalkylaminoalkyl, dialkylaminoalkyl, arylalkanoyl, —SO2-phenyl, and aryl wherein: each such substituent is optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently alkyl, alkoxy, alkoxycarbonyl, halogen, or haloalkyl; R3 is H, halogen, alkoxycarbonyl, arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH2)naryl, arylalkoxy, —OC(O)N(alkyl)(CH2)naryl, aryloxy, arylthio, thioalkoxy, arylthioalkoxy, alkenyl, —NR6R7, NR6R7—(C1-C6)alkyl, or alkyl, wherein: the aryl portion of arylalkoxycarbonyl, aryloxycarbonyl, arylalkyl, —OC(O)NH(CH2)naryl, arylalkoxy, —OC(O)N(alkyl)(CH2)naryl, and arylthioalkoxy is unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently, halogen, alkoxy, alkyl, haloalkyl, or haloalkoxy; R4 is hydrogen or R4 is alkyl unsubstituted or substituted with one or two substituents that are independently CO2R, OH, —CO2—(C1-C6)alkyl, —C(O)NR6R7, —C(O)R6, —N(R30)C(O)NR6R7, —N(R30)C(O)—(C1-C4 alkyl)-NR6R7, —OC(O)NR6R7, —OC(O)—(C1-C6 alkyl), —N(R30)C(O)NR16R17, —N(R30)C(O)—(C1-C6)alkoxy, —N(R30)C(O)—(C1-C4 alkyl)-NR6R7, or —NR6R7, —OC(O)NR17-alkyl-heteroaryl, arylalkoxy, arylalkyl, heteroaryl, heteroarylalkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, R6R7N—(C1-C6 alkyl)-, —NR6R7, alkoxy, carboxaldehyde, —C(O)NR6R7, CO2R, alkoxyalkyl, or alkoxyalkoxy, wherein: the heteroaryl or aryl portions of the above substituents are unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently halogen, hydroxy, alkoxy, alkyl, —CO2—(C1-C6)alkyl, —CONR6R7, —NR6R7, R6R7N—(C1-C6)alkyl-, nitro, haloalkyl, or haloalkoxy; R5 is H, or R5 is aryl, arylalkyl, arylthioalkyl, alkyl optionally substituted with 1, 2, or 3 substituents that are independently arylalkoxycarbonyl, —NR8R9, halogen, —C(O)NR8R9, alkoxycarbonyl, C3-C7 cycloalkyl, or alkanoyl, alkoxy, alkoxyalkyl optionally substituted with one trimethylsilyl, amino, alkoxycarbonyl, hydroxyalkyl, dihydroxyalkyl, alkynyl, —SO2-alkyl, alkoxy optionally substituted with one trimethylsilyl, heterocycloalkylalkyl, cycloalkyl, cycloalkylalkyl, -alkyl-S-aryl, -alkyl-SO2-aryl, heteroarylalkyl, heterocycloalkyl, -heteroaryl-heterocycloalkyl, heteroaryl, or alkenyl optionally substituted with one substituent selected from the group consisting of alkoxycarbonyl, carboxyl, and —OC(O)NR6R7, wherein: each such substituent is unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently alkyl optionally substituted with 1 or 2 substituents that are independently NR16R17, —NR16SO2-alkyl, —NR16SO2-phenyl, —OC(O)NH2, or —OC(O)NR16R17, OH, —OC(O)NR16R17, halogen, alkoxy wherein the alkyl is optionally substituted with NR16R17, —C(O)NR16R17, OH or C1-C4 alkoxy, hydroxyalkyl, dihydroxyalkyl, arylalkoxy, thioalkoxy, alkoxycarbonyl, arylalkoxycarbonyl, CO2R, CN, OH, hydroxyalkyl, dihydroxyalkyl, —SO2NR16R17, amidinooxime, —OC(O)NR6R7, —NR6R7, —NR8R9, R6R7N—(C1-C6 alkyl)-, carboxaldehyde, —S-alkyl wherein the alkyl is optionally substituted with NR16R17, —C(O)NR16R17, OH or C1-C4 alkoxy, SO2alkyl wherein the alkyl is optionally substituted with NR16R17, —C(O)NR16R17, OH or C1-C4 alkoxy, —OC(O)—(C1-C6 alkyl), —SO2H, —SO2NR6R7, alkanoyl wherein the alkyl portion is optionally substituted with OH, halogen, —OC(O)—(C1-C6 alkyl), or alkoxy, —C(O)NR6R7, —(C1-C4 alkyl)-C(O)NR6R7, heterocycloalkyl or heterocycloalkylalkyl, wherein the heterocycloalkyl is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, tetrahydrofuranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR16R17, amidino, haloalkyl, —(C1-C4 alkyl)-NR15C(O)NR16R17, —(C1-C4 alkyl)-NR15C(O)R18, —O—CH2—O, C2-C6 alkenyl optionally substituted with —OC(O)NR6R7, C1-C4 alkoxy, or OH, —O—CH2CH2—O—, or haloalkoxy; R15 is H or C1-C6 alkyl; and R18 is C1-C6 alkyl optionally substituted with —O—(C2-C6 alkanoyl, C1-C6 hydroxyalkyl, C1-C6 dihydroxyalkyl, C1-C6 alkoxy, C1-C6 alkoxy C1-C6 alkyl; amino C1-C6 alkyl, mono or dialkylamino C1-C6 alkyl.

2. A compound according to claim 1, wherein: R1 is halogen, C1-C4 alkyl optionally substituted with C1-C4 alkoxycarbonyl, C2-C4 alkenyl optionally substituted with C1-C4 alkoxycarbonyl, C2-C4 alkynyl, or carboxaldehyde; R3 is H; and R4 is H, alkyl optionally substituted with one or two substituents that are independently CO2R, OH, —CO2alkyl, —C(O)NR6R7, —OC(O)NR6R7, —OC(O)—(C1-C6 alkyl), —C(O)R6, —N(R30)C(O)NR6R7, —N(R30)C(O)—(C1-C6)alkoxy, or —NR6R7, —C(O)NR6R7, phenyl(C1-C6)alkoxy, phenyl(C1-C6)alkyl, hydroxyalkyl, dihydroxyalkyl, haloalkyl, alkoxy, alkoxyalkyl, or alkoxyalkoxy, wherein: the phenyls are unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently halogen, hydroxy, alkoxy, alkyl, nitro, CF3, or OCF3.

3. A compound according to claim 2, wherein: R2 is —OSO2-phenyl, phenylalkoxy, phenyloxy, phenylthioalkoxy, phenylalkynyl, phenyloxy(C1-C6)alkyl, —OC(O)NH(CH2)nphenyl, —OC(O)N(alkyl)(CH2)nphenyl, pyridyl, pyrimidyl, thienyl, piperazinyl, imidazolidinyl, pyrrolidinyl, piperidinyl, tetrahydropyranyl, or tetrahydrofuranyl, wherein: each such substituent is substituted with 1, 2, 3, 4, or 5 substituents wherein at least one substituent is of the formula —(C1-C4 alkyl)-NR6C(O)NR7—(C1-C6 alkoxy), —(C1-C4 alkyl)-NR6C(O)NR7—(C1-C6 alkyl) —(C1-C4 alkyl)-NR16C(O)NR17—(C3-C6 cycloalkylalkyl), —(C1-C4 alkyl)-NR16C(O)NR17-(heteroaryl) wherein the heteroaryl is optionally substituted with C1-C4 alkyl, C1-C4 alkoxy, halogen or OH, haloalkyl, or —(C1-C4 alkyl)-NR16C(O)NR17—(C3-C6 cycloalkyl) and the other substituents, if present, are independently halogen, —NR6R7, CF3, OCF3, C1-C4 alkyl, —(C1-C4)alkyl-C(O)NR6R7, R6R7N—(C1-C6 alkyl)-, —C(O)NR6R7, —(C1-C4 alkyl)-NRC(O)NR16R17, CN, hydroxyalkyl, dihydroxyalkyl, —OC(O)NR6R7, or —(C1-C6)alkyl-N(R)-CO2R30; as to R16 and R17: R16 and R17 at each occurrence are independently H or C1-C6 alkyl; or R16, R17 and the nitrogen to which they are attached form a morpholinyl ring; as to R6 and R7: R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, C1-C6 alkanoyl, phenyl C1-C4 alkyl, heterocycloalkyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, phenyl, heterocyloalkylalkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy; or R6, R7, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, C1-C4 alkoxycarbonyl, hydroxyl, hydroxy C1-C4 alkyl, dihydroxy C1-C4 alkyl, or halogen; n is 0, 1, 2, 3, 4, 5, or 6; R at each occurrence is independently H or C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl; and R30 is C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl.

4. A compound according to claim 3, wherein: R5 is: Z1 is H, halogen, C1-C4 alkyl, CF3, C1-C4 hydroxyalkyl, C1-C4 dihydroxyalkyl, or C1-C4 alkoxy; and Z2 is C1-C4 alkyl, —C(O)NR6R7, —(C1-C4 alkyl)-C(O)NR6R7, —NR6R7, NR6R7(C1-C6 alkyl), C1-C6 hydroxyalkyl, C1-C6 dihydroxyalkyl, halogen, C1-C4 alkoxy, CO2R, OH, C1-C6 alkoxycarbonyl, CF3, or C2-C6 alkenyl optionally substituted with CO2H, or —OC(O)NR16R17; Z3 is H, halogen, C1-C6 alkyl, C1-C6 alkoxy, alkoxyalkyl, —SO2-alkyl or C2-C6 alkenyl, wherein: the alkyl, alkoxy, and alkenyl portions of such substituents are optionally substituted with 1, 2, or 3 substituents that are independently —OC(O)NR16R17, —C(O)NR16R17, OH, or NR16R17; and R6 and R7 at each occurrence are independently H, OH, C1-C6 alkyl optionally substituted with heteroaryl that is selected from thienyl, pyridyl, and furanyl, amino C1-C4 alkyl, NH(C1-C6 alkyl)alkyl, N(C1-C6 alkyl)(C1-C6 alkyl) C1-C6 alkyl, C1-C6 hydroxyalkyl, C1-C6 dihydroxyalkyl, C1-C6 alkoxy C1-C6 alkyl, —SO2(C1-C6 alkyl), —SO2NH2, —SO2NH(C1-C6 alkyl), —SO2N(C1-C6 alkyl)(C1-C6 alkyl), or C1-C6 alkanoyl, each of which is optionally substituted with 1, 2, or 3 substituents that are independently halogen, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy.

5. A compound according to claim 4, wherein: R2 is benzyloxy or phenyl C1-C4 thioalkoxy, each of which is substituted with 1, 2, 3, 4, or 5 substituents, wherein: at least one substituent has the formula —(C1-C4 alkyl)-NR6C(O)NR7—(C1-C6 alkoxy) and the other substituents, if present, are independently halogen, amino, monoalkylamino, dialkylamino, CF3, OCF3, C1-C4 alkyl, CN, hydroxyalkyl, or dihydroxyalkyl; R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or heteroaryl that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, C1-C6 alkanoyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy; and R16 and R17 at each occurrence are independently H or C1-C6 alkyl.

6. A compound according to claim 4, wherein: the compound corresponds in structure to the following formula: k is 0, 1, 2, 3, or 4; R18 is C1-C6 alkyl; and R19 at each occurrence is independently halogen, —NR6R7, CF3, OCF3, C1-C4 alkyl, —(C1-C4)alkyl-C(O)NR6R7, R6R7N—(C1-C6 alkyl)-, —C(O)NR6R7, —(C1-C4 alkyl)-NRC(O)NR16R17, CN, hydroxyalkyl, dihydroxyalkyl, —OC(O)NR6R7, or —(C1-C6)alkyl-N(R)—CO2R30.

7. A compound according to claim 2, wherein: R2 is benzyloxy or phenyl C1-C4 thioalkoxy, each of which is substituted with 1, 2, 3, 4, or 5 substituents independently selected from —(C1-C4 alkyl)-NR6C(O)NR7—(C1-C6 alkoxy), —(C1-C4 alkyl)-NR16C(O)NR17—(C3-C6 cycloalkyl), halogen, amino, monoalkylamino, dialkylamino, CF3, OCF3, C1-C4 alkyl, CN, hydroxyalkyl, or dihydroxyalkyl; as to R6 and R7: R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or heteroaryl that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR16R17, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, OH, C1-C6 alkanoyl, C3-C6 cycloalkyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, —SO2NR16R17, —SO2-C1-C6 alkyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, pyridyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy; or R6, R7, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dionyl, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, C1-C4 alkoxycarbonyl, hydroxyl, hydroxy C1-C4 alkyl, dihydroxy C1-C4 alkyl, or halogen; R16 and R17 at each occurrence are independently H or C1-C6 alkyl; and R4 is H, hydroxyalkyl, or alkyl which is optionally substituted with one or two substituents that are independently CO2R, OH, —CO2alkyl, —C(O)NR6R7, —OC(O)NR6R7, —OC(O)—(C1-C6 alkyl), —C(O)R6, —N(R30)C(O)NR6R7, —N(R30)C(O)—(C1-C4 alkyl)-NR6R7, —N(R30)C(O)—(C1-C6)alkoxy, or —NR6R7.

8. A compound according to claim 7, wherein: R2 is benzyloxy substituted with 1, 2, 3, or 4 substituents that are independently halogen, —NR6R7, C1-C4 haloalkyl, C1-C4 haloalkoxy, C1-C4 alkyl optionally substituted with —(C1-C4 alkyl)-NR(C(O)NR7—(C1-C6 alkoxy), —(C1-C4)alkyl-C(O)NR6R7, R6R7N—(C1-C6 alkyl)-, —C(O)NR6R7, —(C1-C4 alkyl)-NRC(O)NR16R17, CN, hydroxyalkyl, dihydroxyalkyl, —OC(O)NR6R7, or —(C1-C6)alkyl-N(R)—CO2R30; R5 is selected from the group consisting of H, phenyl(C1-C6)alkyl, (C1-C6)alkyl optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently phenyl C1-C4 alkoxycarbonyl, —NR8R9, halogen, —C(O)NR8R9, alkoxycarbonyl, or alkanoyl, phenyl, alkoxy, C2-C6 alkynyl, C2-C6 alkenyl optionally substituted with alkoxycarbonyl, CO2H, or —OC(O)NR16R17, indolyl, indolinyl, quinolinyl, isoquinolinyl, benzothiazolyl, isoindolyl, dihydroindolyl, pyrazolyl, isobenzofuranonyl, imidazolyl, pyridyl, pyrimidyl, pyrazinyl, dihydroisoindolyl, benzimidazolyl, indolon-2-yl, indazolyl, benzimidazolyl, imidazolidine dione, pyrazolyl(C1-C6 alkyl), imidazolyl(C1-C6 alkyl), piperidinyl(C1-C6)alkyl, pyrrolidinyl(C1-C6)alkyl, imidazolidinyl(C1-C6)alkyl, 1H-indazolyl(C1-C6)alkyl, dihydroindolon-2-yl(C1-C6 alkyl), isobenzofuranonyl(C1-C6 alkyl), benzothiazolyl(C1-C6 alkyl), indolinyl(C1-C6 alkyl), dihydrobenzimidazolyl(C1-C6 alkyl), or dihydrobenzoimidazolonyl(C1-C6 alkyl), pyridyl(C1-C6)alkyl, pyridazinyl(C1-C6)alkyl, pyrimidinyl(C1-C6)alkyl, pyrazinyl(C1-C6)alkyl, tetrahydrofuryl(C1-C6)alkyl, naphthyl(C1-C6)alkyl, morpholinyl(C1-C6)alkyl, tetrahydrofuryl(C1-C6)alkyl, thienyl (C1-C6)alkyl, piperazinyl(C1-C6)alkyl, indolyl(C1-C6)alkyl, quinolinyl(C1-C6)alkyl, isoquinolinyl(C1-C6)alkyl, isoindolyl(C1-C6)alkyl, dihydroindolyl(C1-C6)alkyl, pyrazolyl(C1-C4)alkyl, imidazolyl(C1-C4)alkyl, dihydroisoindolyl(C1-C6)alkyl, indolon-2-yl(C1-C6)alkyl, morpholinyl C1-C6 alkyl, -pyrimidinyl-piperazinyl, -pyridinyl-piperazinyl, alkenyl, -alkenyl-CO2-alkyl, and -alkenyl-CO2H, wherein: each such substituent is unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently NR16R17, C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently NR16R17, —NR16SO2-alkyl, —NR16SO2-phenyl, —OC(O)NH2, —OC(O)NHR16, OH, or —OC(O)NR16R17, halogen, —OC(O)NR6R7, C1-C6 alkoxy optionally substituted with NR16R17, phenyl C1-C6 alkoxy, C1-C6 thioalkoxy, C1-C6 alkoxycarbonyl, CO2R, CN, carboxaldehyde, —SO2(C1-C6)alkyl optionally substituted with NR16R17, —SO2NR16R17, amidinooxime, NR8R9, CN, —NR6R7, NR6R7 C1-C6 alkyl, —C(O)NR6R7, —(C1-C4)alkyl-C(O)NR6R7, amidino, C1-C4 haloalkyl, phenyl, hydroxy C1-C6 alkyl, C1-C6 dihydroxyalkyl, C1-C4 haloalkoxy, C2-C6 alkenyl optionally substituted with —OC(O)NR6R7, C1-C4 alkoxy, or OH, —C(O)C(O)NR16R17, heterocycloalkyl or heterocycloalkylalkyl, wherein the heterocycloalkyl is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR16R17, or alkanoyl optionally substituted with OH, halogen, —OC(O)—(C1-C6 alkyl), or C1-C4 alkoxy, wherein: each phenyl and heteroaryl is optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently C1-C4 alkyl, C1-C4 alkoxy, halogen, amino, CF3, or OCF3; each heterocycloalkyl is optionally substituted with 1, 2, 3, or 4 substituents that are independently, C1-C4 alkyl, C1-C4 alkoxy, halogen, C1-C4 alkanoyl, —C(O)NR6R7; R8 is hydrogen, C1-C6 alkyl, C1-C6 alkanoyl, phenyl C1-C6 alkyl and phenyl C1-C6 alkanoyl; and R9 is amino C1-C6 alkyl, mono C1-C6 alkylamino C1-C6 alkyl, di C1-C6 alkylamino C1-C6 alkyl, C1-C6 alkyl, C1-C6 alkanoyl, phenyl C1-C6 alkyl, indazolyl, and phenyl C1-C6 alkanoyl.

9. A compound according to claim 8, wherein: R16 and R17 at each occurrence are independently H or C1-C6 alkyl; as to R6 and R7: R6 and R7 are independently at each occurrence H, alkyl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, C1-C6 alkanoyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, —SO2—C1-C6 alkyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy; or R6, R7, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, C1-C4 alkoxycarbonyl, hydroxyl, hydroxy C1-C4 alkyl, dihydroxy C1-C4 alkyl, or halogen; n is 0, 1, 2, 3, 4, 5 or 6; R5 is pyridyl, pyrimidyl, pyrazinyl, pyridyl(C1-C6)alkyl, pyrimidinyl(C1-C6) alkyl, or pyrazinyl(C1-C6)alkyl wherein: each such substituent is unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently NR16R17, C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently NR16R17, —NR16SO2-alkyl, —NR16SO2-phenyl, —OC(O)NH2, or —OC(O)NR16R17, halogen, —OC(O)NR6R7, C1-C6 alkoxy optionally substituted with NR16R17, phenyl C1-C6 alkoxy, C1-C6 thioalkoxy, C1-C6 alkoxycarbonyl, CO2R, CN, —S(C1-C6)alkyl optionally substituted with NR16R17, —SO2(C1-C6)alkyl optionally substituted with NR16R17, amidinooxime, NR8R9, CN, —NR6R7, NR6R7 C1-C6 alkyl, —C(O)NR6R7, —(C1-C4)alkyl-C(O)NR6R7, amidino, C1-C4 haloalkyl, hydroxy C1-C6 alkyl, C1-C6 dihydroxyalkyl, C1-C4 haloalkoxy, —C(O)C(O)NR16R17, heterocycloalkyl which is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, alkoxyalkyl optionally substituted with NR16R17, or alkanoyl optionally substituted with OH, halogen, —OC(O)—(C1-C6 alkyl), or C1-C4 alkoxy, wherein: each phenyl and heteroaryl is optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently C1-C4 alkyl, C1-C4 alkoxy, halogen, amino, CF3, or OCF3; each heterocycloalkyl is optionally substituted with 1, 2, 3, or 4 substituents that are independently, C1-C4 alkyl, C1-C4 alkoxy, halogen, C1-C4 alkanoyl, —C(O)NR6R7; R8 is hydrogen, C1-C4 alkyl, C1-C4 alkanoyl, benzyl, and phenyl C1-C4 alkanoyl; and R9 is amino C1-C6 alkyl, mono C1-C6 alkylamino C1-C6 alkyl, di C1-C6 alkylamino C1-C6 alkyl, C1-C6 alkyl, C1-C6 alkanoyl, phenyl C1-C6 alkyl, indazolyl, and phenyl C1-C6 alkanoyl.

10. A compound according to claim 9, wherein: R1 is halogen; R4 is hydroxyalkyl or C1-C4 alkyl optionally substituted with one or two substituents that are independently CO2R, —CO2alkyl, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)NH(C1-C6 alkyl)(C1-C6 alkyl), —C(O)-C1-C6 alkyl, —N(R30)C(O)NR16R17, or —N(R30)C(O)—(C1-C6)alkoxy; R5 is pyridyl, pyrimidyl, pyrazinyl, pyridyl(C1-C6)alkyl, pyrimidinyl(C1-C6) alkyl, or pyrazinyl(C1-C6)alkyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently NR16R17, C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently NR16R17, —NR16SO2-alkyl, —NR16SO2-phenyl, —OC(O)NH2, or —OC(O)NR16R17, halogen, —OC(O)NR6R7, C1-C6 alkoxy optionally substituted with NR16R17, —SO2(C1-C6 alkyl) optionally substituted with NR16R17, —SO2(C1-C6)alkyl optionally substituted with NR16R17, NR8R9, CN, NR6R7 C1-C6 alkyl, —C(O)NR6R7, —NR6R7, heterocycloalkyl which is selected from the group consisting of piperazinyl, piperidinyl, and pyrrolidinyl, or alkoxyalkyl optionally substituted with NR16R17, wherein: each phenyl and heteroaryl are optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently C1-C4 alkyl, C1-C4 alkoxy, halogen, amino, CF3, or OCF3; each heterocycloalkyl is optionally substituted with 1, 2, 3, or 4 substituents that are independently, C1-C4 alkyl, C1-C4 alkoxy, halogen, C1-C4 alkanoyl, —C(O)NR6R7; R8 is hydrogen, C1-C4 alkyl, C1-C4 alkanoyl, benzyl, and phenyl C1-C4 alkanoyl; and R9 is amino C1-C6 alkyl, mono C1-C6 alkylamino C1-C6 alkyl, di C1-C6 alkylamino C1-C6 alkyl, C1-C6 alkyl, C1-C6 alkanoyl, phenyl C1-C6 alkyl, and phenyl C1-C6 alkanoyl.

11. A compound according to claim 10, wherein: R5 is of the formula: R50 is NR16R17, alkyl optionally substituted with 1, 2, or 3 substituents that are independently —NR16R17, —NR16SO2alkyl, or —NR16CO2C1-C6 alkyl, alkoxy optionally substituted with NR16R17, —S(C1-C6 alkyl) optionally substituted with NR16R17, —SO2(C1-C6 alkyl) optionally substituted with NR16R17, piperazinyl optionally substituted with 1 or 2 substituents that are independently H, alkyl, alkanoyl, or CONR6R7, -alkyl-NR16SO2phenyl wherein the phenyl is optionally substituted with 1, 2, 3, 4 or 5 substituents that are independently halogen, alkyl, alkoxy, or CONR16R17, alkoxyalkyl optionally substituted with NR16R17, or -alkyl-OC(O)NR16R17, NR8R9, CN, NR6R7 C1-C6 alkyl, —C(O)NR6R7, —NR6R7, R51 is H C1-C4 alkyl, C1-C4 alkoxy, or halogen; and R6 and R7 are independently H, C1-C4 alkyl, hydroxyalkyl, C1-C6 alkanoyl, —SO2—C1-C6 alkyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy.

12. A compound according to claim 10, wherein: R5 is of the formula: R6 and R7 are independently H, C1-C4 alkyl, hydroxyalkyl, C1-C6 alkanoyl, —SO2—C1-C6 alkyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy.

13. A compound according to claim 10, wherein: R5 is of the formula: R55 is —(C1-C6 alkyl)-NR6R7, or —NR6R7; and R6 and R7 are independently H, C1-C4 alkyl, hydroxyalkyl, C1-C6 alkanoyl, —SO2—C1-C6 alkyl, wherein: each such substituent is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy.

14. A compound according to claim 10, wherein: R5 is of the formula: each R60 is independently H, —C(O)NR6R7, —CO2R, C1-C4 hydroxyalkyl, C2-C6 dihydroxyalkyl, —(C1-C6 alkyl)-NR6R7, halogen, C2-C6 alkenyl, CN, or —NR6R7; R6 and R7 are independently H, C1-C4 alkyl, C1-C6 alkanoyl, wherein the alkyl portion of each of the above is optionally substituted with OH, or halogen; and R at each occurrence is independently H or C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, SH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl.

15. A compound according to claim 10, wherein: R5 is: R60 is —SO2-C1-C6 alkyl, or —(C1-C6 alkyl)-NR6R7; R6 and R7 are independently H, C1-C4 alkyl, C1-C6 alkanoyl, wherein: the alkyl portion of each of the above substituents is optionally substituted with OH or halogen; R at each occurrence is independently H or C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, SH, halogen, amino; monoalkylamino, dialkylamino or C3-C6 cycloalkyl; and R61 is H, C1-C4 alkyl, C1-C4 alkoxy, or halogen.

16. A compound according to claim 8, wherein: R5 is C2-C6 alkenyl -alkenyl-CO2-alkyl, and -alkenyl-CO2H, each of which is optionally substituted with —NR6R7, OH, —C(O)NR6R7; and as to R6 and R7: R6 and R7 at each occurrence are independently H, alkyl optionally substituted with heteroaryl that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, C1-C6 alkanoyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, —SO2-C1-C6 alkyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each of the above is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, CF3, or OCF3; or R6, R7, and the nitrogen to which they are attached form a morpholinyl, piperidinyl, pyrrolidinyl, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, C1-C4 alkoxycarbonyl, hydroxyl, hydroxy C1-C4 alkyl, dihydroxy C1-C4 alkyl, or halogen.

17. A compound according to claim 8, wherein: R5 is phenyl optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently NR16R17, C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently NR16R17, —NR16SO2-alkyl, —NR6SO2-phenyl, —OC(O)NH2, —OC(O)NHR16, OH, or —OC(O)NR16R17, halogen, —OC(O)NR6R7, C1-C6 alkoxy optionally substituted with NR16R17, phenyl C1-C6 alkoxy, C1-C6 thioalkoxy, C1-C6 alkoxycarbonyl, CO2R, CN, carboxaldehyde, —SO2(C1-C6)alkyl optionally substituted with NR16R17, —SO2NR16R17, amidinooxime, NR8R9, —NR6R7, NR6R7 C1-C6 alkyl, —C(O)NR6R7, —(C1-C4)alkyl-C(O)NR6R7, amidino, CF3, phenyl, C1-C6 hydroxyalkyl, C1-C6 dihydroxyalkyl, OCF3, C2-C6 alkenyl optionally substituted with —OC(O)NR6R7, C1-C4 alkoxy, or OH, —C(O)C(O)NR16R17, heterocycloalkyl which is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR16R17, or alkanoyl optionally substituted with OH, halogen, —OC(O)—(C1-C6 alkyl), or C1-C4 alkoxy, wherein: each phenyl and heteroaryl is optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently C1-C4 alkyl, C1-C4 alkoxy, halogen, amino, CF3, or OCF3; and each heterocycloalkyl is optionally substituted with 1, 2, 3, or 4 substituents that are independently, C1-C4 alkyl, C1-C4 alkoxy, halogen, C1-C4 alkanoyl, —C(O)NR16R17; as R6 and R7: R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or heteroaryl that is selected from thienyl, pyridyl, and furanyl, C1-C6 hydroxyalkyl, C2-C6 dihydroxyalkyl, NR16R17, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, OH, C1-C6 alkanoyl, C3-C6 cycloalkyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, —SO2-C1-C6 alkyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, pyridyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each of the above substituents is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy; or R6, R7, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dione, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, C1-C4 alkoxycarbonyl, hydroxyl, hydroxy C1-C4 alkyl, dihydroxy C1-C4 alkyl, or halogen; and R at each occurrence is independently H or C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl.

18. A compound according to claim 8, wherein: R5 is phenyl(C1-C4)alkyl, which is optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently NR16R17, C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently NR16R17, —NR16SO2-alkyl, —NR16SO2-phenyl, —OC(O)NH2, —OC(O)NHR16, OH, or —OC(O)NR16R17, halogen, —OC(O)NR6R7, C1-C6 alkoxy optionally substituted with NR16R17, phenyl C1-C6 alkoxy, C1-C6 thioalkoxy, C1-C6 alkoxycarbonyl, CO2R, CN, carboxaldehyde, —SO2(C1-C6)alkyl optionally substituted with NR16R17, —SO2NR16R17, amidinooxime, NR8R9, CN, —NR6R7, NR6R7 C1-C6 alkyl, —C(O)NR6R7, —(C1-C4)alkyl-C(O)NR6R7, amidino, C1-C4 haloalkyl, phenyl, hydroxy C1-C6 alkyl, C1-C6 dihydroxyalkyl, C1-C4 haloalkoxy, C2-C6 alkenyl optionally substituted with —OC(O)NR6R7, C1-C4 alkoxy, or OH, —C(O)C(O)NR16R17, heterocycloalkyl which is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR16R17, or alkanoyl optionally substituted with 1 or 2 substituents that are independently OH, halogen, —OC(O)—(C1-C6 alkyl), or C1-C4 alkoxy; wherein: each phenyl and heteroaryl is optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently C1-C4 alkyl, C1-C4 alkoxy, halogen, amino, CF3, or OCF3; each heterocycloalkyl is optionally substituted with 1, 2, 3, or 4 substituents that are independently, C1-C4 alkyl, C1-C4 alkoxy, halogen, C1-C4 alkanoyl, —C(O)NR16R17; as to R6 and R7: R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or heteroaryl that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR16R17, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, OH, C1-C6 alkanoyl, C3-C6 cycloalkyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, —SO2NR16R17, —SO2-C1-C6 alkyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, pyridyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-c4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each of the above substituents is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy; or R6, R7, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dione, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, C1-C4 alkoxycarbonyl, hydroxyl, hydroxy C1-C4 alkyl, dihydroxy C1-C4 alkyl, or halogen; and R at each occurrence is independently H or C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl.

19. A compound according to claim 8, wherein: R5 is selected from the group consisting of H, (C1-C6)alkyl optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently phenyl C1-C4 alkoxycarbonyl, —NR8R9, halogen, —C(O)NR8R9, alkoxycarbonyl, or alkanoyl, indolyl, indolinyl, quinolinyl, isoquinolinyl, benzothiazolyl, isoindolyl, dihydroindolyl, pyrazolyl, 3H-isobenzofuran-1-onyl, imidazolyl, pyridyl, pyrimidyl, pyrazinyl, furanyl, dihydroisoindolyl, indolon-2-yl, indazolyl, thienyl, benzimidazolyl, imidazolidine dione, pyrazolyl(C1-C6 alkyl), furanyl(C1-C6 alkyl), imidazolyl(C1-C6 alkyl), piperidinyl(C1-C6)alkyl, pyrrolidinyl(C1-C6)alkyl, imidazolidinyl(C1-C6)alkyl, 1H-indazolyl(C1-C6)alkyl, dihydroindolon-2-yl(C1-C6 alkyl), 3H-isobenzofuranonyl(C1-C6 alkyl), benzothiazolyl(C1-C6 alkyl), indolinyl(C1-C6 alkyl), dihydrobenzimidazolyl(C1-C6 alkyl), benzimidazolyl(C1-C6)alkyl, isochroman-4-one (C1-C6)alkyl, oxazolidin-2-one (C1-C6)alkyl, benzoxazolyl(C1-C6)alkyl, dihydrobenzoimidazolonyl(C1-C6 alkyl), pyridyl(C1-C6)alkyl, pyridazinyl(C1-C6)alkyl, pyrimidinyl(C1-C6)alkyl, pyrazinyl(C1-C6)alkyl, tetrahydrofuryl(C1-C6)alkyl, naphthyl(C1-C6)alkyl, morpholinyl(C1-C6)alkyl, tetrahydrofuryl(C1-C6)alkyl, thienyl (C1-C6)alkyl, piperazinyl(C1-C6)alkyl, indolyl(C1-C6)alkyl, quinolinyl(C1-C6)alkyl, isoquinolinyl(C1-C6)alkyl, dihydro-1H-isoindolyl(C1-C6)alkyl, dihydroindolyl(C1-C6) alkyl, imidazolyl(C1-C4)alkyl, dihydroisoindolyl(C1-C6)alkyl, indolon-2-yl(C1-C6)alkyl, morpholinyl C1-C6 alkyl, -pyrimidinyl-piperazinyl, and -pyridinyl-piperazinyl, wherein: each of the above substituents is unsubstituted or substituted with 1, 2, 3, 4, or 5 substituents that are independently NR16R17, C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently NR16R17, —NR16SO2-alkyl, —NR16SO2-phenyl, —OC(O)NH2, —OC(O)NHR16, OH, or —OC(O)NR16R17, halogen, —OC(O)NR6R7, C1-C6 alkoxy optionally substituted with NR16R17, phenyl C1-C6 alkoxy, C1-C6 thioalkoxy, C1-C6 alkoxycarbonyl, CO2R, CN, carboxaldehyde, —SO2(C1-C6)alkyl optionally substituted with NR16R17, —SO2NR16R17, amidinooxime, NR8R9, CN, —NR6R7, NR6R7 C1-C6 alkyl, —C(O)NR6R7, —(C1-C4)alkyl-C(O)NR6R7, amidino, C1-C4 haloalkyl, phenyl, hydroxy C1-C6 alkyl, C1-C6 dihydroxyalkyl, C1-C4 haloalkoxy, C2-C6 alkenyl optionally substituted with —OC(O)NR6R7, C1-C4 alkoxy, or OH, —C(O)C(O)NR16R17, heterocycloalkyl or heterocycloalkyl(C1-C6)alkyl, wherein the heterocycloalkyl is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, heteroaryl which is selected from the group consisting of pyridyl, furanyl, pyrazolyl, and thienyl, alkoxyalkyl optionally substituted with NR16R17, or alkanoyl optionally substituted with OH, halogen, C3-C6 cycloalkyl, —OC(O)—(C1-C6 alkyl), or C1-C4 alkoxy; wherein: each phenyl and heteroaryl is optionally substituted with 1, 2, 3, 4, or 5 substituents that are independently C1-C4 alkyl, C1-C4 alkoxy, halogen, amino, CF3, or OCF3; each heterocycloalkyl is optionally substituted with 1, 2, 3, or 4 substituents that are independently, C1-C4 alkyl, C1-C4 alkoxy, halogen, C1-C4 alkanoyl, —C(O)NR16R17; as to R6 and R7: R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or heteroaryl that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR16R17, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, OH, C1-C6 alkanoyl, C3-C6 cycloalkyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, —SO2NR16R17, —SO2-C1-C6 alkyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, pyridyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each of the above substituents is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy; or R6, R7, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dione, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, C1-C4 alkoxycarbonyl, hydroxyl, hydroxy C1-C4 alkyl, dihydroxy C1-C4 alkyl, or halogen; and R at each occurrence is independently H or C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl.

20. A compound according to claim 19, wherein: R5 is indolyl(C1-C6)alkyl-, indolinyl-(C1-C4 alkyl)-, isochroman-4-one (C1-C6) alkyl-, indolon-2-yl(C1-C6)alkyl-, benzoxazolyl(C1-C6)alkyl-, 3H-isobenzofuran-1-one (C1-C6)alkyl-, 3H-isobenzofuran-1-one, dihydro-1H-isoindolyl(C1-C6)alkyl, dihydroisoindolyl(C1-C6)alkyl, benzothiazolyl(C1-C6)alkyl-, benzothiazolyl, benzimidazolyl, or benzimidazolyl(C1-C6)alkyl-, optionally substituted with 1, 2, 3, or 4 substituents that are independently C1-C4 alkyl, OH, —C(O)C(O)NR16R17, piperidinyl(C1-C4)alkyl, piperazinyl(C1-C6)alkyl, pyrrolidinyl(C1-C4)alkyl, NR6R7 C1-C6 alkyl, morpholinyl C1-C6 alkyl, C1-C6 alkanoyl optionally substituted with 1 or 2 substituents that are independently OH, halogen, —OC(O)—(C1-C6 alkyl), or C1-C4 alkoxy, —SO2(C1-C6)alkyl, C1-C6 alkoxycarbonyl; and R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or heteroaryl that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR16R17, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, OH, C1-C6 alkanoyl, C3-C6 cycloalkyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, —SO2NR16R17, —SO2-C1-C6 alkyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, pyridyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each of the above substituents is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy.

21. A compound according to claim 19, wherein: R5 is pyrazolyl C1-C6 alkyl, oxazolidin-2-one (C1-C6)alkyl, furanyl, thienyl, or furanyl C1-C6 alkyl, wherein: each such substituent is optionally substituted with 1 or 2 substituents independently selected from the group consisting of —C(O)NR6R7, NR6R7 C1-C6 alkyl, C1-C6 alkyl, C1-C6 alkoxycarbonyl, (C1-C4)alkyl optionally substituted with 1 or 2 substituents that are independently NR16R17, —NR16SO2-alkyl, —NR16SO2-phenyl, —OC(O)NH2, —OC(O)NHR16, OH, or —OC(O)NR16R17, hydroxy C1-C6 alkyl, heterocycloalkyl which is selected from the group consisting of morpholinyl, piperazinyl, tetrahydropyranyl, piperidinyl, pyrrolidinyl, and imidazolidinyl, CO2R, C3-C6 cycloalkyl, as to R6 and R7: R6 and R7 are independently at each occurrence H, alkyl optionally substituted with NR16R17 or a heteroaryl group that is selected from thienyl, pyridyl, and furanyl, hydroxyalkyl, dihydroxyalkyl, NR16R17, alkoxy optionally substituted with NR16R17, C1-C4 alkoxy C1-C4 alkyl, OH, C1-C6 alkanoyl, C3-C6 cycloalkyl, phenyl C1-C4 alkyl, tetrahydropyranyloxy, tetrahydrofuranyloxy, piperidinyloxy, pyrrolidinyloxy, C2-C6 alkenyl optionally substituted with —OC(O)NR16R17, —SO2-phenyl, —SO2NR16R17, —SO2—C1-C6 alkyl, phenyl, pyrrolidinyl C1-C4 alkanoyl, piperidinyl C1-C4 alkanoyl, pyridyl C1-C4 alkanoyl, phenyl C1-C4 alkoxy, phenyl C1-C4 alkoxycarbonyl, or phenyl C1-C4 alkanoyl, wherein: each of the above substituents is unsubstituted or substituted with 1, 2, or 3 substituents that are independently, halogen, C3-C6 cycloalkyl, amino, monoalkylamino, dialkylamino, —C(O)NH2, —C(O)NH(C1-C6 alkyl), —C(O)N(C1-C6 alkyl)(C1-C6 alkyl), C1-C4 alkoxy, C1-C4 alkyl, OH, SH, carboxaldehyde, piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl, —OC(O)C1-C6 alkyl, C1-C4 haloalkyl, or C1-C4 haloalkoxy; or R6, R7, and the nitrogen to which they are attached form a morpholinyl, thiomorpholinyl, thiomorpholinyl S-oxide, thiomorpholinyl S,S-dioxide, piperidinyl, pyrrolidinyl, isoindole 1,3-dione, or piperazinyl ring which is optionally substituted with 1 or 2 substituents that are independently C1-C4 alkyl, C1-c4 alkoxycarbonyl, hydroxyl, hydroxy C1-C4 alkyl, dihydroxy C1-C4 alkyl, or halogen; and R at each occurrence is independently H or C1-C6 alkyl optionally substituted with 1 or 2 substituents that are independently OH, halogen, amino, monoalkylamino, dialkylamino or C3-C6 cycloalkyl.

22. A compound according to claim 1, wherein the compound is selected from the group consisting of: (2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]but-2-enoic acid; 3-[4-{[2-({[(Cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide; 3,5-dibromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-methyl-2-(methylsulfonyl)pyrimidin-5-yl]pyridin-2(1H)-one; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-4-(morpholin-4-ylcarbonyl)benzamide; 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carboxylic acid; 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluorobenzamide; 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(tetrahydro-2H-pyran-2-yloxy)benzamide; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzamide; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-3-(trifluoromethyl)benzamide; 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-hydroxy-4-methylbenzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(1E)-3-hydroxyprop-1-en-1-yl]phenyl}-6-methylpyridin-2(1H)-one; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(tetrahydro-2H-pyran-2-yloxy)benzamide; (2E)-3-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}prop-2-en-1-yl carbamate; 1-[5-(aminomethyl)-2-methylphenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride; N-{3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzyl}-2-hydroxyacetamide; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(hydroxymethyl)phenyl]-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(2E)-4-morpholin-4-yl-4-oxobut-2-en-1-yl]pyridin-2(1H)-one; tert-butyl {3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}carbamate; N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)urea; 2-[(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)amino]-1-methyl-2-oxoethyl acetate; methyl 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furoate; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(1-glycoloyl-2,3-dihydro-1H-indol-5-yl)methyl]pyridin-2(1H)-one; N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-hydroxypropanamide; N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-hydroxy-2-methylpropanamide; 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide; 2-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}-2-hydroxyethyl carbamate; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzamide; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide; {1-[3-(aminocarbonyl)phenyl]-5-chloro-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl carbamate; 2-({3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}amino)-2-oxoethyl acetate; 2-({3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-fluorophenyl}amino)-1,1-dimethyl-2-oxoethyl acetate; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzamide; N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N-methylurea; 1-[4-(aminomethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[5-(morpholin-4-ylcarbonyl)-2-furyl]pyridin-2(1H)-one; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl carbamate; {5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-furyl}methyl carbamate; 3-bromo-2-[2-(2-fluorophenyl)pyridin-4-yl]-1,5,6,7-tetrahydro-4H-pyrrolo[3,2-c]pyridin-4-one trifluoroacetate; N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-2-hydroxy-2-methylpropanamide; 1-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorophenyl}ethane-1,2-diyl dicarbamate; 1-[4-(aminomethyl)-2-fluorophenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride; 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-2-oxoethyl acetate; 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-1,1-dimethyl-2-oxoethyl acetate; 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-indol-2-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(1H-pyrazol-3-ylmethyl)pyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(1H-pyrazol-3-ylmethyl)pyridin-2(1H)-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxyethyl)-1H-pyrazol-3-yl]methyl}-6-methylpyridin-2(1H)-one; 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzenesulfonamide; {1-[3-(aminocarbonyl)phenyl]-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate; 1-(1,3-benzoxazol-6-ylmethyl)-3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one; {1-[3-(aminocarbonyl)phenyl]-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl carbamate; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)-2-furamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[5-(morpholin-4-ylcarbonyl)-2-furyl]methyl}pyridin-2(1H)-one; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-2-furamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(4-vinylphenyl)pyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[5-(piperazin-1-ylcarbonyl)-2-furyl]methyl}pyridin-2(1H)-one; methyl 2-bromo-5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzoate; N-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}urea; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylamino)pyrimidin-5-yl]methyl}pyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[5-(hydroxymethyl)-2-furyl]methyl}-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)phenyl]-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[5-(piperidin-1-ylcarbonyl)-2-furyl]pyridin-2(1H)-one; methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]benzoate; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[1-(methylsulfonyl)-2,3-dihydro-1H-indol-5-yl]methyl}pyridin-2(1H)-one; 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-2-oxoethyl acetate; 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2,3-dihydro-1H-indol-1-yl)-1,1-dimethyl-2-oxoethyl acetate 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-cyclopropyl-4-methylbenzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(1H-pyrazol-3-ylmethyl)pyridin-2(1H)-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(methoxyacetyl)-1H-pyrazol-3-yl]methyl}-6-methylpyridin-2(1H)-one; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-ethyl-4-methylbenzamide; N-allyl-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide; {1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate; 4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]methyl}-N-methylbenzamide; 1-{[5-(aminomethyl)pyrazin-2-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one; 2-{[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]amino}-2-oxoethyl acetate; N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-hydroxyacetamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(dimethylamino)pyrimidin-5-yl]methyl}-6-methylpyridin-2(1)-one trifluoroacetate; methyl 3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoate; 1-allyl-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)pyridin-2(1H)-one; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-butyl-4-methylbenzamide; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carbonitrile; N-(2-aminoethyl)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide hydrochloride; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-1-{4-[(methylamino)methyl]benzyl}pyridin-2(1H)-one; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-isobutyl-4-methylbenzamide; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[1-(2-hydroxy-2-methylpropyl)-1H-pyrazol-3-yl]methyl}-6-methylpyridin-2(1H)-one; ethyl 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-5-carboxylate; 3-[3-chloro-4-{[2-({[(cyclobutylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide; N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]acetamide; N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]methanesulfonamide; methyl [(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]carbamate; N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-hydroxy-2-methylpropanamide; N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-1-hydroxycyclopropanecarboxamide; N1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]glycinamide hydrochloride; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(3-oxo-1,3-dihydro-2-benzofuran-5-yl)pyridin-2(1H)-one; 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzenesulfonamide; tert-butyl 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1,3-dihydro-2H-isoindole-2-carboxylate; methyl 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)-2-oxopyridin-1(2H)-yl]-4-methylbenzoate; 1-{[2-(aminomethyl)pyrimidin-5-yl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate; N1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)methyl]glycinamide trifluoroacetate; 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-hydroxy-1-(hydroxymethyl)ethyl]-4-methylbenzamide; methyl 5-bromo-2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-2-oxopyridin-1(2H)-yl]benzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methyl-5-vinylphenyl)pyridin-2(1H)-one; 1-[(2-aminopyrimidin-5-yl)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-methoxypyrimidin-5-yl)methyl]-6-methylpyridin-2(1H)-one; 3-[6-(aminomethyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzamide hydrochloride; methyl 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-vinylbenzoate; 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-(dimethylamino)ethyl]-4-methylbenzamide; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-vinylbenzoic acid; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidine-2-carboxamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)alaninamide hydrochloride; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N2-methylglycinamide hydrochloride; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)serinamide hydrochloride; N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)prolinamide hydrochloride; dimethyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]isophthalate; methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-vinylbenzoate; methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(1,2-dihydroxyethyl)benzoate; 3-[3-chloro-4-{[2-({[(cyclopropylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide; N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)methyl]-2-hydroxyacetamide; 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-methyl-1,3-dihydro-2H-indol-2-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,3-dihydro-1H-isoindol-5-ylmethyl)-6-methylpyridin-2(1H)-one trifluoroacetate; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyridine-2-carboxamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(E)-2-methoxyvinyl]phenyl}-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2,6-difluoro-4-[(Z)-2-methoxyvinyl]phenyl}-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[2,6-difluoro-4-(2-hydroxyethyl)phenyl]-6-methylpyridin-2(1H)-one; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-2-vinylbenzamide; 5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1-methyl-1,3-dihydro-2H-indol-2-one; methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(1-hydroxy-1-methylethyl)benzoate; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-(1,2-dihydroxyethyl)-N-methylbenzamide; N1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-D-alaninamide hydrochloride; N1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-N2-methylglycinamide hydrochloride; N1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-D-serinamide hydrochloride; 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one; 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[2-(2-hydroxy-2-methylpropanoyl)-2,3-dihydro-1H-isoindol-5-yl]methyl}-6-methylpyridin-2(1H)-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-dimethyl-1,3-benzothiazol-5-yl)-6-methylpyridin-2(1H)-one; 3-[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furoic acid; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-(trifluoromethyl)benzoic acid; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N,N-dimethyl-3-(trifluoromethyl)benzamide; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-fluorobenzoic acid; 1-[5-(aminomethyl)-2-fluorophenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3,5-difluorobenzoic acid; (2E)-4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxy-2-methylpropyl)but-2-enamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(5-hydroxy-1H-pyrazol-3-yl)-2-methylphenyl]-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(hydroxymethyl)-2-furyl]-6-methylpyridin-2(1H)-one; methyl 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-[(methylamino)methyl]benzoate; (−)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{2-(hydroxymethyl)-5-[(methylamino)methyl]phenyl}-6-methylpyridin-2(1H)-one; 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-(2-hydroxyethyl)-2-furamide; 1-[4-(aminomethyl)-2-fluorophenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[4-methyl-2-(methylsulfonyl)pyrimidin-5-yl]pyridin-2(1H)-one; 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N1-(2-hydroxyethyl)-N4-methylterephthalamide; 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carbonitrile; methyl 3-[4-[(2,4-difluorobenzyl)oxy]-2-methyl-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoate; 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylpyrimidine-2-carboxamide; 3-chloro-1-{[1-(Cyclopropylcarbonyl)-1H-pyrazol-3-yl]methyl}-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one; 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylthiophene-3-carboxamide; {1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl phenylcarbamate; {1-allyl-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl [2-(3-thienyl)ethyl]carbamate; methyl 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoate; 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzoic acid; 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}-N-methylbenzamide; 4-{1-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]ethyl}benzamide; (+)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-{1-[4-(hydroxymethyl)phenyl]ethyl}-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-oxopropyl)pyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(hydroxymethyl)-3-(1-hydroxy-1-methylethyl)phenyl]-6-methylpyridin-2(1H)-one; 1-[2,4-bis(1-hydroxy-1-methylethyl)phenyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one; 5-bromo-2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methylbenzamide; 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-5-vinylbenzamide; 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(1,2-dihydroxyethyl)-N-methylbenzamide; 3-[3-bromo-4-{[2-({[(ethyl amino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methyl-N-(2,2,2-trifluoroethyl)benzamide; 3-bromo-1-(3′-chloro-4-methylbiphenyl-3-yl)-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one; 2-(5-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]methyl}-1H-indol-3-yl)-N,N-dimethyl-2-oxoacetamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluoro-4-glycoloylphenyl)-6-methylpyridin-2(1H)-one; N-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)-2-hydroxy-2-methylpropanamide; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(piperidin-1-ylmethyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one; N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)piperidine-4-carboxamide hydrochloride; N2-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrimidin-2-yl)glycinamide; N-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-hydroxy-2-methylpropanamide; 3-[3-bromo-4-{[2-({[(ethylamino)carbonyl]amino}methyl)-4-fluorobenzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N-[2-(dimethylamino)ethyl]-4-methylbenzamide; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(piperazin-1-ylmethyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one hydrochloride; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-D-serinamide hydrochloride; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-L-threoninamide hydrochloride; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-methylalaninamide hydrochloride; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-D-alaninamide hydrochloride; N-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)piperidine-4-carboxamide hydrochloride; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-{[2-(dimethylamino)ethyl]amino}pyrimidin-5-yl)methyl]-6-methylpyridin-2(1H)-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-({3-[(dimethylamino)methyl]-1H-indol-5-yl}methyl)pyridin-2(1H)-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-({3-[(methylamino)methyl]-1H-indol-5-yl}methyl)pyridin-2(1H)-one; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-N2-methyl-L-serinamide hydrochloride; N-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyridin-2-yl)-2-hydroxy-2-methylpropanamide; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[(3-{[(2-hydroxyethyl)amino]methyl}-1H-indol-5-yl)methyl]pyridin-2(1H)-one; N1-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-L-serinamide hydrochloride; N1-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}phenyl)-2-methylalaninamide hydrochloride; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-D-allothreoninamide hydrochloride; N1-(4-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-2-methylalaninamide hydrochloride; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(morpholin-4-ylmethyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-({2-[(2-hydroxyethyl)amino]pyrimidin-5-yl}methyl)-6-methylpyridin-2(1H)-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-({[2-(dimethylamino)ethyl]amino}methyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one; 1-({2-[(2-aminoethyl)amino]pyrimidin-5-yl}methyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one trifluoroacetate; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-hydroxy-N,4-dimethylbenzamide; N-(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)-2-hydroxyacetamide; 3-[3-bromo-4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide; 1-allyl-6-[(allylamino)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]pyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(2-hydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one; N1-(4-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}benzyl)-L-threoninamide hydrochloride; N1-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}glycinamide hydrochloride; 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-[2-(dimethylamino)ethyl]-1H-pyrazole-5-carboxamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2-{[2-hydroxy-1-(hydroxymethyl)ethyl]amino}pyrimidin-5-yl)methyl]-6-methylpyridin-2(1H)-one; 3-[3-bromo-4-{[4-fluoro-2-({[(methoxyamino)carbonyl]amino}methyl)benzyl]oxy}-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzamide; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methylpyridine-2-carboxamide; 1-{[5-(aminomethyl)-2-furyl]methyl}-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methylpyridin-2(1H)-one hydrochloride; N-(2-{[(3-bromo-1-{5-[(2,2-dimethylhydrazino)carbonyl]-2-methylphenyl}-6-methyl-2-oxo-1,2-dihydropyridin-4-yl)oxy]methyl}-5-fluorobenzyl)-N′-ethylurea; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-{[3-(pyrrolidin-1-ylmethyl)-1H-indol-5-yl]methyl}pyridin-2(1H)-one; 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-methoxyethyl)-1H-pyrazole-5-carboxamide; 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-2-vinylbenzamide; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-hydroxy-4-methylbenzamide; 3-[3-bromo-4-(2,4-difluoro-benzyloxy)-6-methyl-2-oxo-2H-pyridin-1-yl]-N-carbamoylmethyl-benzamide; N1-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}-N2-methylglycinamide hydrochloride; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,5-dimethyl-1H-benzimidazol-6-yl)-6-methylpyridin-2(1H)-one; 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1H-pyrazole-5-carboxamide; 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2,3-dihydroxypropyl)-1H-pyrazole-5-carboxamide; 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-1H-pyrazole-5-carboxamide; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-(2,3-dihydro-1H-isoindol-5-ylmethyl)pyridin-2(1H)-one trifluoroacetate; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,4′-bipyridine-2′-carboxamide; 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-(2-hydroxyethyl)-1H-pyrazole-5-carboxamide; N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-2-furyl)methyl]-2-hydroxy-2-methylpropanamide; N1-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}alaninamide hydrochloride; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(2-methylprop-2-en-1-yl)pyridin-2(1H)-one; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one; 5-bromo-6-[(2,4-difluorobenzyl)oxy]-3-isopropyl-2-[4-(2-methylalanyl)piperazin-1-yl]pyrimidin-4(3H)-one trifluoroacetate; methyl 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,4′-bipyridine-2′-carboxylate; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[5-(2-furyl)-2-methylphenyl]-6-methylpyridin-2(1H)-one; N1-{4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzyl}serinamide hydrochloride; 5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethylpyridine-2-carboxamide; 3-{[3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N-methyl-1H-pyrazole-5-carboxamide; N1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-D-alaninamide hydrochloride; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-[(glycylamino)methyl]-2-oxopyridin-1(2H)-yl]benzamide hydrochloride; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(4-hydroxy-1-oxo-3,4-dihydro-1H-isochromen-7-yl)-6-methylpyridin-2(1H)-one; 6-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}nicotinamide; N1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-2-methylalaninamide hydrochloride; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,4′-bipyridine-2′-carboxylic acid; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-{[(N-methylglycyl)amino]methyl}-2-oxopyridin-1(2H)-yl]benzamide hydrochloride; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxo-6-[(serylamino)methyl]pyridin-1(2H)-yl]benzamide hydrochloride; N1-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]-D-serinamide hydrochloride; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(3-methyl-4-vinylphenyl)pyridin-2(1H)-one; N-[(5-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]urea; N-[(S-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}pyrazin-2-yl)methyl]piperidine-4-carboxamide hydrochloride; 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-N,N-dimethyl-1H-pyrazole-5-carboxamide; {5-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[(2E)-4-hydroxybut-2-en-1-yl]-6-oxo-1,6-dihydropyridin-2-yl}methyl acetate; 3-[6-[(alanylamino)methyl]-3-bromo-4-[(2,4-difluorobenzyl)oxy]-2-oxopyridin-1(2H)-yl]benzamide hydrochloride; 3-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-(3-methyl-1H-pyrazol-4-yl)pyridin-2(1H)-one; N-({1-[3-(aminocarbonyl)phenyl]-5-bromo-4-[(2,4-difluorobenzyl)oxy]-6-oxo-1,6-dihydropyridin-2-yl}methyl)pyridine-2-carboxamide; methyl 2-bromo-5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]benzoate; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-2′-(hydroxymethyl)-6-methyl-2H-1,4′-bipyridin-2-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-[4-(1,2-dihydroxyethyl)-3-methylphenyl]-6-methylpyridin-2(1H)-one; N-({3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,3′-bipyridin-6′-yl}methyl)-2-hydroxy-2-methylpropanamide; 6′-(aminomethyl)-3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2H-1,3′-bipyridin-2-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-({2-[2-(dimethylamino)ethoxy]pyrimidin-5-yl}methyl)-6-methylpyridin-2(1H)-one; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-{[(2-methylalanyl)amino]methyl}-2-oxopyridin-1(2H)-yl]benzamide hydrochloride; 3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-{[(2-hydroxy-2-methylpropanoyl)amino]methyl}-2-oxopyridin-1(2H)-yl]benzamide; 3-bromo-6′-chloro-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-2H-1,3′-bipyridin-2-one; 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(hydroxymethyl)-N-methylbenzamide; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-[(methylamino)carbonyl]benzyl carbamate; 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-[(methylamino)carbonyl]benzyl carbamate; 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-vinylbenzoic acid; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,3′-bipyridine-6′-carboxamide; methyl 4-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-3-[(methylamino)carbonyl]benzoate; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2′-vinyl-2H-1,4′-bipyridin-2-one; 5-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-2-(1,2-dihydroxyethyl)-N-methylbenzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-6′-vinyl-2H-1,3′-bipyridin-2-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[2-(methylsulfonyl)pyrimidin-5-yl]pyridin-2(1H)-one; 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-formyl-N-methylbenzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxo-2H-1,3′-bipyridine-6′-carbonitrile; methyl 3-bromo-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-2-oxo-2H-1,3′-bipyridine-6′-carboxylate; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-[(2-oxo-1,3-oxazolidin-5-yl)methyl]pyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6′-(1,2-dihydroxyethyl)-5′,6-dimethyl-2H-1,3′-bipyridin-2-one; 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-N-methyl-5-[(methylamino)methyl]benzamide; 3-bromo-2′-chloro-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2H-1,4′-bipyridin-2-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-5′,6-dimethyl-2-oxo-2H-1,3′-bipyridine-6′-carboxamide; (−)-3-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-4-methylbenzoic acid; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-2′-(1,2-dihydroxyethyl)-6-methyl-2H-1,4′-bipyridin-2-one; 2-[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]-5-(1-hydroxy-1-methylethyl)-N-methylbenzamide; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-1-(3,3-dimethyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)-6-methylpyridin-2(1H)-one; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-(hydroxymethyl)pyridin-2(1H)-one; 3-[3-bromo-4-[(2,4-difluorophenoxy)methyl]-6-methyl-2-oxopyridin-1(2H)-yl]-N,4-dimethylbenzamide; 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-5-fluoro-N-(1-methyl-1H-pyrazol-3-yl)benzamide; 2-({[3-bromo-1-(2,6-difluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridin-4-yl]oxy}methyl)-N-(Cyclopropylmethyl)-5-fluorobenzamide; 3-{[3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-2-oxopyridin-1(2H)-yl]methyl}-1-tetrahydro-2H-pyran-2-yl-1H-pyrazole-5-carboxylic acid; 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylsulfonyl)pyrimidin-5-yl]methyl}pyridin-2(1H)-one; and 3-bromo-4-[(2,4-difluorobenzyl)oxy]-6-methyl-1-{[2-(methylthio)pyrimidin-5-yl]methyl}pyridin-2(1H)-one.

23. A compound according to claim 3, wherein: the compound corresponds in structure to the following formula: R1 is halogen; and Z, R20, and R30 are as defined below; ZR20R30—CH2CH3HH—CH2CH3H—CH2CH3H—CH2CH3H—CH2CH3H—CH2CH3MeH—CH2CH3Me—CH2CH3Me—CH2CH3FH—CH2CH3F—CH2CH3F—CH2CH3F—CH2CH3F—OCH3HH—OCH3H—OCH3H—OCH3H—OCH3H—OCH3MeH—OCH3Me—OCH3Me—OCH3Me—OCH3Me—OCH3FH—OCH3F—OCH3F—OCH3F—OCH3F—CH(CH3)2HH—CH(CH3)2H—CH(CH3)2H—CH(CH3)2H—CH(CH3)2H—CH(CH3)2MeH—CH(CH3)2Me—CH(CH3)2Me—CH(CH3)2Me—CH(CH3)2Me—CH(CH3)2FH—CH(CH3)2F—CH(CH3)2F—CH(CH3)2F—CH(CH3)2F

24. A compound according to claim 3, wherein: the compound corresponds in structure to the following formula: R1 is halogen; and Z, R20, and R30 are as defined below: ZR20R30—CH2CH3HH—CH2CH3H—CH2CH3H—CH2CH3H—CH2CH3H—CH2CH3MeH—CH2CH3Me—CH2CH3Me—CH2CH3FH—CH2CH3F—CH2CH3F—CH2CH3F—CH2CH3FH—OCH3HH—OCH3H—OCH3H—OCH3H—OCH3H—OCH3MeH—OCH3Me—OCH3Me—OCH3Me—OCH3Me—OCH3FH—OCH3F—OCH3F—OCH3F—OCH3F—CH(CH3)2HH—CH(CH3)2H—CH(CH3)2H—CH(CH3)2H—CH(CH3)2H—CH(CH3)2MeH—CH(CH3)2Me—CH(CH3)2Me—CH(CH3)2Me—CH(CH3)2Me—CH(CH3)2FH—CH(CH3)2F—CH(CH3)2F—CH(CH3)2F—CH(CH3)2F

25. A compound according to claim 3, wherein: the compound corresponds in structure to the following formula: Y is: CONH(CH2)nOH; CONHCH2C(Me)2OH; CONH(CH2)nNH2; CONH(CH2)nNHCH3; CONH(CH2)nN(CH3)2; CONHCH2CH(OH)CH2OH; CH2NHCOCH2NH2; CH2NHCOCH2OH; or CH2NHCOCH(NH2)CH2OH; and n is 1, 2, or 3.

26. A compound according to claim 3, wherein: the compound corresponds in structure to the following formula: R50 is: —O(CH2)nR51; —NH(CH2)nR51; —N(CH3)(CH2)nR51; —S(CH2)nR51; —SO2(CH2)nR51; n is 2, 3, or 4; R51 is H, OH, NH2, NHR52, CONHR52, or OR52; R52 is H or C1-C4 alkyl; and R53 is H or alkyl.

27. A compound according to claim 3, wherein: the compound corresponds in structure to the following formula: R50 is: CH2CONH2; CH2CONHCH3; CH2CONH(CH3)2; CH2CONH(CH2)nNH2; CH2CONH(CH2)nNHCH3; CH2NHCONH2; CH2NHCO(CH2)2NH2; CH2NHCH3; CH2N(CH3)2; CH2NHSO2 (C1-C3 alkyl); CH2NHSO2 phenyl; CH2NHCOCH(alkyl)NH2; CH2NHCOCH(CH2OH)NH2; CH2OCONH2; CH2O(CH2)2NH2; CONHCH3; CONH2; CON(CH3)2; CONH(CH2)nNH2; CONH(CH2)nNHCH3; or CONH(CH2)nN(CH3)2; and n is 1, 2, or 3.