HIV protease inhibitors, compositions containing the same, their pharmaceutical uses and materials for their synthesis

BACKGROUND OF THE INVENTION

[0002] 1. Field of the Invention

[0003] This invention relates to novel compounds useful as HIV protease inhibitors and to the use of such compounds as antiviral agents for treatment of HIV infected individuals. This invention also relates to methods of preparation of these compounds and to intermediates that are useful in the preparation thereof.

[0004] 2. Related Background Art

[0005] Acquired Immune Deficiency Syndrome (AIDS) causes a gradual breakdown of the body's immune system as well as progressive deterioration of the central and peripheral nervous systems. Since its initial recognition in the early 1980's, AIDS has spread rapidly and has now reached epidemic proportions within a relatively limited segment of the population. Intensive research has led to the discovery of the responsible agent, human T-lymphotropic retrovirus III (HTLV-III), now more commonly referred to as the human immunodeficiency virus or HIV.

[0006] HIV is a member of the class of viruses known as retroviruses. The retroviral genome is composed of RNA which is converted to DNA by reverse transcription. This retroviral DNA is then stably integrated into a host cell's chromosome and, employing the replicative processes of the host cells, produces new retroviral particles and advances the infection to other cells. HIV appears to have a particular affinity for the human T-4 lymphocyte cell which plays a vital role in the body's immune system. HIV infection of these white blood cells depletes this white cell population. Eventually, the immune system is rendered inoperative and ineffective against various opportunistic diseases such as, among others, pneumocystic carini pneumonia, Kaposi's sarcoma, and cancer of the lymph system.

[0007] Although the exact mechanism of the formation and working of the HIV virus is not understood, identification of the virus has led to some progress in controlling the disease. For example, the drug azidothymidine (AZT) has been found effective for inhibiting the reverse transcription of the retroviral genome of the HIV virus, thus giving a measure of control, though not a cure, for patients afflicted with AIDS. The search continues for drugs that can cure or at least provide an improved measure of control of the deadly HIV virus.

[0008] Retroviral replication routinely features post-translational processing of polyproteins. This processing is accomplished by virally encoded HIV protease enzyme. This yields mature polypeptides that will subsequently aid in the formation and function of infectious virus. If this molecular processing is stifled, then the normal production of HIV is terminated. Therefore, inhibitors of HIV protease may function as anti-HIV viral agents.

[0009] HIV protease is one of the translated products from the HIV structural protein pol gene. This retroviral protease specifically cleaves other structural polypeptides at discrete sites to release these newly activated structural proteins and enzymes, thereby rendering the virion replication-competent. As such, inhibition of the HIV protease by potent compounds may prevent proviral integration of infected T-lymphocytes during the early phase of the HIV-1 life cycle, as well as inhibit viral proteolytic processing during its late stage. Additionally, the protease inhibitors may have the advantages of being more readily available, longer lived in virus, and less toxic than currently available drugs, possibly due to their specificity for the retroviral protease.

[0010] Related inhibitors of HIV proteases have been described in, e.g., U.S. Pat. No. 5,962,640, U.S. Pat. No. 5,932,550, Australian Patent No. 705193, Canadian Patent Application No. 2,179,935, Europan Patent Application No. 0 751 145, and Japanese Patent Application No.100867489. Other related HIV protease inhibitors have been described in K. Yoshimura, et al., Proct. Natl. Acad. Sci. USA, 96 8675-8680 (1999) and T. Mimoto, et al., J. Med. Chem., 42, 1789-1802 (1999).

[0011] On-going treatment of HIV-infected individuals with compounds that inhibit HIV protease has led to the development of mutant viruses that possess protesases that are resistant to the inhibitory effect of these compounds. Thus, to be effective, new HIV protease inhibitors must be effective not only against wild-type strains of HIV, but must also demonstrate efficacy against the newly emerging mutant strains that are resistant to the commercially available protease inhibitors. Accordingly, there continues to be a need for new inhibitors targeting the HIV protease in both wild type and mutant strains of HIV.

SUMMARY OF THE INVENTION

[0012] This invention relates to compounds useful for inhibiting the activity of HIV-protease of Formula I:

[0013] wherein:

[0014] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0015] V is C═O, C═S or SO2;

[0016] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, a heterocyclic-aliphatic group or N(R2a)R2b, wherein R2a is an aliphatic, carbocyclic or heterocyclic group, and R is H or a C1-C6 aliphatic group;

[0017] W is N, O, C or CH;

[0018] when W is N, C or CH, R2′ is H or a C1-C6 aliphatic group or R2 and R2′ taken together with the atom W to which they are attached form an unsubstituted or substituted carbocyclic or heterocyclic ring;

[0019] when W is O, R2′ is absent;

[0020] X is

[0021] where Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group;

[0022] n is O, 1 or 2;

[0023] Rx is H or one or more substituents independently selected from C1-C6 alkyl, nitro, amino, cyano, halogen, C1-C6 haloalkyl, hydroxyl, C1-C6 alkoxy, alkylenedioxy, C1-C6 alkylcarbonyl, C1-C6 alkyloxycarbonyl, C1-C6 alkylcarbonyloxy, carboxyl, carbamoyl, formyl, C1-C6 alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, di-C1-C6-alkylaminothiocarbonyl, C1-C6 alkylsulfonyl, C1-C6 alkylsulfenyl, C1-C6 alkylcarbonylamino, C1-C6 alkylthiocarbonylamino, C1-C6 alkylsulfonyloxy, C1-C6 alkylsulfonylamino, mercapto, and C1-C6 alkylthio;

[0024] R8 and R8′ are each independently H, halo or a C1-C4 aliphatic group;

[0025] A is CH2, CH(RA) or is absent;

[0026] Z is S, O, SO, SO2, CH2, CHF, CF2, CH(OH), CH(O—RZ), CH(N—RZRZ′), CH(S—RZ), C(═O), or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group and RZ′ is H or a C1-C6 aliphatic group;

[0027] or RA and RZ, taken together with A and Z form an unsubstituted or substituted 5 or 6 membered carbocyclic or heterocyclic ring;

[0028] R3 is H or a C1-C6 aliphatic group;

[0029] R4 and R5 are independently selected from H, halo, a C1-C6 aliphatic group or a group having the formula C(O)R4′, wherein R4′ is an aliphatic, carbocyclic or heterocyclic group;

[0030] or R4 and R5, taken together with the atom to which they are bound, form an unsubstituted or substituted carbocyclic ring;

[0031] or R4 and R6 or R7, together with the atoms to which they are bound, form an unsubstituted or substituted carbocyclic ring;

[0032] R6 and R7 are independently selected from H, halo or a C1-C6 aliphatic group;

[0033] or R6 and R7, taken together with the atom to which they are bound, form an unsubstituted or substituted carbocyclic or heterocyclic group;

[0034] wherein any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0035] wherein any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic;

[0036] provided that R2 is not an aliphatic group, a phenyl group or a phenyl-substituted aliphatic group when A is absent; Z is S, SO, SO2, CHF, O or CH2; V is C═O; W is N; R2′, R3, R8 and R8′ are H; R4, R5, R6 and R7 are H or a C1-C6 alkyl groups.

[0037] X is

[0038] wherein Rx is H; and R1 is a substituted or unsubstituted 5 or 6-membered mono-cyclic carbocyclic or heterocyclic group;

[0039] or provided that R2 is not t-butyl when R1 is substituted or unsubstituted phenyloxymethylene, or quinolylmethyenecarbonylaminomethylene; A is absent; Z is S; V is C═O; W is N; R2′, R3, R4, R5, R8 and R8′ are H; R6 and R7 are H, methyl, ethyl or propyl; and X is

[0040] wherein Rx is H or methoxy.

[0041] The present invention relates to compounds of Formula I below, and prodrugs, pharmaceutically active metabolites, and pharmaceutically acceptable salts and solvates thereof that inhibit the protease encoded by human immunodeficiency virus (HIV) type 1 (HIV-1) or type 2 (HIV-2), as well as mutant strains thereof. These compounds are useful in the treatment of infection by HIV and the treatment of the acquired immune deficiency syndrome (AIDS). The compounds, their pharmaceutically acceptable salts, and the pharmaceutical compositions of the present invention can be used alone or in combination with other antivirals, immunomodulators, antibiotics or vaccines. Compounds of the present invention can also be converted to prodrugs, by derivatization, according to conventional techniques. Methods of treating AIDS, methods of treating HIV infection and methods of inhibiting HIV protease are disclosed.

DETAILED DESCRIPTION OF INVENTION AND PREFERRED EMBODIMENTS

[0042] In the compounds of this invention, the aliphatic groups are optionally substituted by one or more suitable substituents selected from aryl, cycloalkyl, heterocycloalkyl, heteroaryl, nitro, amino, cyano, halogen, hydroxyl, alkoxy, alkylenedioxy, aryloxy, cycloalkoxy, heterocycloalkoxy, heteroaryloxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, arylcarbonyl, arylcarbonyloxy, aryloxycarbonyl, cycloalkylcarbonyl, cycloalkylcarbonyloxy, cycloalkyoxycarbonyl, heteroarylcarbonyl, heteroarylcarbonyloxy, heteroaryloxycarbonyl, heterocycloalkylcarbonyl, heterocycloalkylcarbonyloxy, heterocycloalkyoxycarbonyl, carboxyl, carbamoyl, formyl, keto (oxo), thioketo, sulfo, alkylamino, cycloalkylamino, arylamino, heterocycloalkylamino, heteroarylamino, dialkylamino, alkylaminocarbonyl, cycloalkylaminocarbonyl, arylaminocarbonyl, heterocycloalkylaminocarbonyl, heteroarylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, cycloalkylaminothiocarbonyl, arylaminothiocarbonyl, heterocycloalkylaminothiocarbonyl, heteroarylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, arylsulfonyl, alkylsulfenyl, arylsulfenyl, alkylcarbonylamino, cycloalkylcarbonylamino, arylcarbonylamino, heterocycloalkylcarbonylamino, heteroarylcarbonylamino, alkylthiocarbonylamino, cycloalkylthiocarbonylamino, arylthiocarbonylamino, heterocycloalkylthiocarbonylamino, heteroarylthiocarbonylamino, alkylsulfonyloxy, arylsulfonyloxy, alkylsulfonylamino, arylsulfonylamino, mercapto, alkylthio, haloalkylthio, arylthio, heteroarylthio, wherein any of the alkyl, alkylene, aryl, cycloalkyl, heterocycloalkyl, heteroaryl moieties present in the above substituents may be further substituted. The alkyl, alkylene, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl moieties of any of the above substituents may be optionally substituted by one or more of alkyl (except for alkyl), haloalkyl, aryl, nitro, amino, alkylamino, dialkylamino, halogen, hydroxyl, alkoxy, haloalkoxy, aryloxy, mercapto, alkylthio or arylthio groups.

[0043] In the compounds of this invention the substituted carbocyclic or heterocyclic groups may be optionally substituted by one or more of the following: alkyl, alkenyl, alkynyl, aryl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl, heteroaryl, nitro, amino, cyano, halogen, hydroxyl, alkoxy, alkenyloxy, alkynyloxy, alkylenedioxy, aryloxy, cycloalkoxy, cycloalkenyloxy, heterocycloalkoxy, heterocycloalkenyloxy, heteroaryloxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, arylcarbonyl, arylcarbonyloxy, aryloxycarbonyl, cycloalkylcarbonyl, cycloalkylcarbonyloxy, cycloalkyoxycarbonyl, heteroarylcarbonyl, heteroarylcarbonyloxy, heteroaryloxycarbonyl, heterocycloalkylcarbonyl, heterocycloalkylcarbonyloxy, heterocycloalkyoxycarbonyl, carboxyl, carbamoyl, formyl, keto (oxo), thioketo, sulfo, alkylamino, cycloalkylamino, arylamino, heterocycloalkylamino, heteroarylamino, dialkylamino, alkylaminocarbonyl, cycloalkylaminocarbonyl, arylaminocarbonyl, heterocycloalkylaminocarbonyl, heteroarylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, cycloalkylaminothiocarbonyl, arylaminothiocarbonyl, heterocycloalkylaminothiocarbonyl, heteroarylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, arylsulfonyl, alkylsulfenyl, arylsulfenyl, alkylcarbonylamino, cycloalkylcarbonylamino, arylcarbonylamino, heterocycloalkylcarbonylamino, heteroarylcarbonylamino, alkylthiocarbonylamino, cycloalkylthiocarbonylamino, arylthiocarbonylamino, heterocycloalkylthiocarbonylamino, heteroarylthiocarbonylamino, alkylsulfonyloxy, arylsulfonyloxy, alkylsulfonylamino, arylsulfonylamino, mercapto, alkylthio, haloalkylthio, arylthio, heteroarylthio, wherein any of the alkyl, alkylene, aryl, cycloalkyl, heterocycloalkyl, heteroaryl moieties present in the above substituents may be further substituted. Preferred “suitable substituents” include alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, halogen, hydroxyl, alkoxy, alkylenedioxy, aryloxy, cycloalkoxy, heteroaryloxy, alkylthio, haloalkylthio and carboxyl. The alkyl, alkylene, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl moieties of any of the above substituents may be optionally substituted by one or more of: alkyl, haloalkyl, nitro, amino, alkylamino, dialkylamino, halogen, hydroxyl, alkoxy, haloalkoxy, mercapto, alkylthio.

[0044] In accordance with a convention used in the art,

[0045] is used in structural formulas herein to depict the bond that is the point of attachment of the moiety or substituent to the core or backbone structure.

[0046] As used herein, the term “aliphatic” represents a saturated or unsaturated, straight- or branched-chain hydrocarbon, containing 1 to 10 carbon atoms which may be unsubstituted or substituted by one or more of the substituents described below. The term “aliphatic” is intended to encompass alkyl, alkenyl and alkynyl groups.

[0047] As used herein, the term “alkyl” represents a straight- or branched-chain saturated or unsaturated hydrocarbon, containing 1 to 10 carbon atoms which may be unsubstituted or substituted by one or more of the substituents described below. Exemplary alkyl substituents include, but are not limited to methyl (Me), ethyl (Et), propyl, isopropyl, butyl, isobutyl, t-butyl, and the like. The term “lower alkyl” refers to an alkyl group containing from 1 to 6 carbon atoms

[0048] The term “alkenyl” represents a straight- or branched-chain hydrocarbon, containing one or more carbon-carbon double bonds and having 2 to 10 carbon atoms which may be unsubstituted or substituted by one or more of the substituents described below. Exemplary alkenyl substituents include, but are not limited to ethenyl, propenyl, butenyl, allyl, pentenyl and the like.

[0049] The term “alkynyl” represents a straight- or branched-chain hydrocarbon, containing one or more carbon-carbon triple bonds and having 2 to 10 carbon atoms which may be unsubstituted or substituted by one or more of the substituents described below. An alkynyl moiety may also contain one or more carbon-carbon double bonds. Exemplary alkynyl substituents include, but are not limited to ethynyl, butynyl, propynyl (propargyl) isopropynyl, pentynyl, hexynyl and the like.

[0050] The term “carbocyclic” represents a saturated, partially saturated, or fully unsaturated (aromatic) cyclic hydrocarbon group containing from 3 to 14 carbon atoms which may be unsubstituted or substituted by one or more of the substituents described herein below. The term “carbocyclic” is intended to encompass mono-, bi- and tri-cyclic saturated, partially saturated, or fully unsaturated hydrocarbon groups; for example, cycloalkyl, cycloalkenyl and aryl groups. The term “carbocyclic” is also intended to encompass bi- and tri-cyclic hydrocarbon groups which contain any combination of ring moieties that are saturated, partially saturated, or fully unsaturated (aromatic). Partially saturated carbocycles include, for example, dihydroarenes (e.g., indanyl) or tetra-hydro-arenes (e.g. tetrahydronaphthalene), wherein any one or more points of saturation may occur in any ring moiety of the carbocycle. In addition, it is understood that bonding between any bi- or tri-cyclic carbocyclic group and any other substituent or variable group may be made at any suitable position of the carbocycle. The term “carbocyclic-aliphatic” group is intended to encompass aliphatic groups having a carbocyclic substituent (e.g., phenylmethyl-(benzyl), phenylethyl-, cyclopropylmethyl-, etc.), wherein the carbocyclic moiety and the aliphatic moiety thereof may be independently substituted by one or more suitable substituents.

[0051] “Cycloalkyl” represents a group comprising a non-aromatic monocyclic, bicyclic, or tricyclic hydrocarbon containing from 3 to 14 carbon atoms which may be unsubstituted or substituted by one or more of the substituents described below. Exemplary cycloalkyls include monocyclic rings having from 3-8 carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like. Illustrative examples of cycloalkyl groups include the following:

[0052] “Cycloalkenyl” represents a group comprising a non-aromatic monocyclic, bicyclic, or tricyclic hydrocarbon containing from 4 to 14 carbon atoms which may be unsubstituted or substituted by one or more of the substituents described below and contains at least one carbon-carbon double bond. Exemplary monocyclic cycloalkenyls include groups having from 4-8, preferably 5-6, carbon atoms, such as cyclopentenyl, cyclopentadienyl, cyclohexenyl, cycloheptenyl and the like. Illustrative examples of cycloalkenyl groups include the following:

[0053] “Aryl” represents a group comprising an aromatic, monovalent monocyclic, bicyclic, or tricyclic radical containing from 6 to 18 carbon ring atoms, which may be unsubstituted or substituted by one or more of the substituents described below. Illustrative examples of aryl groups include the following:

[0054] The term “carbocyclic” also to encompasses mixed bi- and tri-cyclic cycloalkyl/cycloalkenyl/aryl groups, which may be unsubstituted or substituted by one or more of the substituents described below. Illustrative examples of such mixed bi-and tri-cyclic groups include the following:

[0055] It is understood that bonding or substitution of any bi-cyclic or tri-cyclic carbocyclic or heterocyclic group described herein may be at any suitable position on any ring. Illustrative examples of such bonding in mixed bi-and tri-cyclic carbocyclic groups include the following:

[0056] wherein R′ is any suitable substituent.

[0057] The term “heterocyclic” represents a saturated, partially saturated, or fully unsaturated (aromatic) cyclic group containing from 3 to 18 ring atoms, which includes 1 to 5 heteroatoms selected from nitrogen, oxygen and sulfur, and which may be unsubstituted or substituted by one or more of the substituents described herein below. The term “heterocyclic” is intended to encompass mono-, bi- and tri-cyclic saturated, partially saturated, or fully unsaturated heteroatom-containing cyclic groups; for example, heterocycloalkyl, heterocycloalkenyl and heteroaryl groups. The term “heterocyclic” is also intended to encompass bi- and tri-cyclic groups which contain any combination of ring moieties that are saturated, partially saturated, or fully unsaturated (aromatic). Partially saturated heterocycles include, for example, dihydroheteroarenes (e.g., dihydroindole) or tetrahydro-heteroarenes (e.g. tetrahydroquinoline), wherein any one or more points of saturation may occur in any ring moiety of the heterocycle. In addition, it is understood that bonding between any bi- or tri-cyclic heterocyclic group and any other substituent or variable group may be made at any suitable position of the heterocycle (i.e., there is no restriction that a substituent or variable group must be bonded to the heteroatom-containing moiety of a bi- or tri-cyclic heterocyclic group). The term “heterocyclic-aliphatic” group is intended to encompass aliphatic groups having a heterocyclic substituent (e.g., pyridylmethyl-, thiazolylmethyl-, tetrahydrofuranylmethyl-, etc.) wherein the heterocyclic moiety and the aliphatic moiety thereof may be independently substituted by one or more suitable substituents.

[0058] “Heterocycloalkyl” represents a group comprising a saturated monovalent monocyclic, bicyclic, or tricyclic radical, containing 3 to 18 ring atoms, which includes 1 to 5 heteroatoms selected from nitrogen, oxygen and sulfur, and which may be unsubstituted or substituted by one or more of the substituents described below. Illustrative examples of heterocycloalkyl groups include, but are not limited to, azetidinyl, pyrrolidyl, piperidyl, piperazinyl, morpholinyl, tetrahydro-2H-1,4-thiazinyl, tetrahydrofuryl, tetrahydropyranyl, 1,3-dioxolanyl, 1,3-dioxanyl, 1,4-dioxanyl, 1,3-oxathiolanyl, 1,3-oxathianyl, 1,3-dithianyl, azabicylo[3.2.1]octyl, azabicylo[3.3.1]nonyl, azabicylo[4.3.0]nonyl, oxabicylo[2.2.1]heptyl, 1,5,9-triazacyclododecyl, and the like. Illustrative examples of heterocycloalkyl groups include the following:

[0059] wherein R is H, alkyl, hydroxyl or represents a compound according to Formula I, and the bond depicted as “” represents bonding to either face of the bi-cyclic moiety (i.e., endo or exo).

[0060] The term “heterocycloalkenyl” is used herein to represent a non-aromatic, monovalent monocyclic, bicyclic, or tricyclic radical, containing 4 to 18 ring atoms, which may include from 1 to 5 heteroatoms selected from nitrogen, oxygen and sulfur, and which may be unsubstituted or substituted by one or more of the substituents described below and which contains at least one carbon-carbon or carbon-heteroatom double bond. Exemplary monocyclic heterocycloalkenyls include groups having from 4-8, preferably 5-6, ring atoms. Illustrative examples of heterocycloalkenyl groups include, but are not limited to, dihydrofuryl, dihydropyranyl, isoxazolinyl, dihydropyridyl, tetrahydropyridyl, and the like. Illustrative examples of heterocycloalkenyl groups include the following:

[0061] wherein R is H, alkyl, hydroxyl or represents a compound according to Formula I.

[0062] “Heteroaryl” represents a group comprising an aromatic monovalent monocyclic, bicyclic, or tricyclic radical, containing 5 to 18 ring atoms, including 1 to 5 heteroatoms selected from nitrogen, oxygen and sulfur, which may be unsubstituted or substituted by one or more of the substituents described below. As used herein, the term “heteroaryl” is also intended to encompass the N-oxide derivative (or N-oxide derivatives, if the heteroaryl group contains more than one nitrogen such that more than one N-oxide derivative may be formed) of the nitrogen-containing heteroaryl groups described herein. Illustrative examples of heteroaryl groups include, but are not limited to, thienyl, pyrrolyl, imidazolyl, pyrazolyl, furyl, isothiazolyl, furazanyl, isoxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl, benzo[b]thienyl, naphtho[2,3-b]thianthrenyl, isobenzofuranyl, chromenyl, xanthenyl, phenoxathienyl, indolizinyl, isoindolyl, indolyl, indazolyl, purinyl, isoquinolyl, quinolyl, phthalazinyl, naphthyridinyl, quinoxyalinyl, quinzolinyl, benzothiazolyl, benzimidazolyl, tetrahydroquinolinyl, cinnolinyl, pteridinyl, carbazolyl, beta-carbolinyl, phenanthridinyl, acridinyl, perimidinyl, phenanthrolinyl, phenazinyl, isothiazolyl, phenothiazinyl, and phenoxazinyl. Illustrative examples of N-oxide derivatives of heteroaryl groups include, but are not limited to, pyridyl N-oxide, pyrazinyl N-oxide, pyrimidinyl N-oxide, pyridazinyl N-oxide, triazinyl N-oxide, isoquinolyl N-oxide, and quinolyl N-oxide. Further examples of heteroaryl groups include the following moieties:

[0063] wherein R is H, alkyl, hydroxyl or represents a compound according to Formula I.

[0064] The term “heterocyclic” also to encompasses mixed bi- and tri-cyclic heterocycloalkyl/heterocycloalkenyl/heteroaryl groups, which may be unsubstituted or substituted by one or more of the substituents described below. Illustrative examples of such mixed bi-and tri-cyclic heterocyclic groups include the following:

[0065] Illustrative examples of such bonding in mixed bi-and tri-cyclic heterocyclic groups include the following:

[0066] wherein R′ is any suitable substituent.

[0067] Unless otherwise stated, exemplary “suitable substituents” that may be present on any of the above aliphatic, carbocyclic, heterocyclic, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl or heteroaryl groups, described herein, include alkyl (except for alkyl), aryl, cycloalkyl, heterocycloalkyl, heteroaryl, nitro, amino, cyano, halogen, hydroxyl, alkoxy, alkylenedioxy, aryloxy, cycloalkoxy, heterocycloalkoxy, heteroaryloxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, arylcarbonyl, arylcarbonyloxy, aryloxycarbonyl, cycloalkylcarbonyl, cycloalkylcarbonyloxy, cycloalkyoxycarbonyl, heteroarylcarbonyl, heteroarylcarbonyloxy, heteroaryloxycarbonyl, heterocycloalkylcarbonyl, heterocycloalkylcarbonyloxy, heterocycloalkyoxycarbonyl, carboxyl, carbamoyl, formyl, keto (oxo), thioketo, sulfo, alkylamino, cycloalkylamino, arylamino, heterocycloalkylamino, heteroarylamino, dialkylamino, alkylaminocarbonyl, cycloalkylaminocarbonyl, arylaminocarbonyl, heterocycloalkylaminocarbonyl, heteroarylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, cycloalkylaminothiocarbonyl, arylaminothiocarbonyl, heterocycloalkylaminothiocarbonyl, heteroarylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, arylsulfonyl, alkylsulfenyl, arylsulfenyl, alkylcarbonylamino, cycloalkylcarbonylamino, arylcarbonylamino, heterocycloalkylcarbonylamino, heteroarylcarbonylamino, alkylthiocarbonylamino, cycloalkylthiocarbonylamino, arylthiocarbonylamino, heterocycloalkylthiocarbonylamino, heteroarylthiocarbonylamino, alkylsulfonyloxy, arylsulfonyloxy, alkylsulfonylamino, arylsulfonylamino, mercapto, alkylthio, arylthio, heteroarylthio, wherein any of the alkyl, alkylene, aryl, cycloalkyl, heterocycloalkyl, heteroaryl moieties present in the above substituents may be further substituted. The alkyl, alkylene, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl moieties of any of the above substituents may be optionally substituted by one or more of alkyl (except for alkyl), haloalkyl, aryl, nitro, amino, alkylamino, dialkylamino, halogen, hydroxyl, alkoxy, haloalkoxy, aryloxy, mercapto, alkylthio or arylthio groups.

[0068] If the substituents themselves are not compatible with the synthetic methods of this invention, the substituent may be protected with a suitable protecting group that is stable to the reaction conditions used in these methods. The protecting group may be removed at a suitable point in the reaction sequence of the method to provide a desired intermediate or target compound. Suitable protecting groups and the methods for protecting and de-protecting different substituents using such suitable protecting groups are well known to those skilled in the art; examples of which may be found in T. Greene and P. Wuts, Protecting Groups in Chemical Synthesis (3rd ed.), John Wiley & Sons, NY (1999), which is incorporated herein by reference in its entirety. In some instances, a substituent may be specifically selected to be reactive under the reaction conditions used in the methods of this invention. Under these circumstances, the reaction conditions convert the selected substituent into another substituent that is either useful in an intermediate compound in the methods of this invention or is a desired substituent in a target compound.

[0069] In the compounds of this invention, R1 and R2′ independently or taken together, may be a suitable nitrogen protecting group. As indicated above, nitrogen protecting groups are well known in the art and any nitrogen protecting group that is useful in the methods of preparing the compounds of this invention or may be useful in the HIV protease inhibitory compounds of this invention may be used. Exemplary nitrogen protecting groups include alkyl, substituted alkyl, carbamate, urea, amide, imide, enamine, sulfenyl, sulfonyl, nitro, nitroso, oxide, phosphinyl, phosphoryl, silyl, organometallic, borinic acid and boronic acid groups. Examples of each of these groups, methods for protecting nitrogen moieties using these groups and methods for removing these groups from nitrogen moieties are disclosed in T. Greene and P. Wuts, supra. Preferably, when R2 and/or R2′ are independently suitable nitrogen protecting groups, suitable R2 and R2′0 substituents include, but are not limited to, carbamate protecting groups such as alkyloxycarbonyl (e.g., Boc: t-butyloxycarbonyl) and aryloxycarbonyl (e.g., Cbz: benzyloxycarbonyl, or FMOC: fluorene-9-methyloxycarbonyl), alkyloxycarbonyls (e.g., methyloxycarbonyl), alkyl or arylcarbonyl, substituted alkyl, especially arylalkyl (e.g., trityl (triphenylmethyl), benzyl and substituted benzyl), and the like. When R2 and R2′ taken together are a suitable nitrogen protecting group, suitable R2/R2′ substituents include phthalimido and a stabase (1,2-bis (dialkylsilyl))ethylene).

[0070] The terms “halogen” and “halo” represent chloro, fluoro, bromo or iodo substituents. “Heterocycle” is intended to mean a heteroaryl or heterocycloalkyl group.

[0071] “Acyl” is intended to mean a —C(O)—R radical, where R is a substituted or unsubstituted alkyl, cycloalkyl, aryl, heterocycloalkyl or heteroaryl group. “Acyloxy” is intended to mean an —OC(O)—R radical, where R is a substituted or unsubstituted alkyl, cycloalkyl, aryl, heterocycloalkyl or heteroaryl group. “Thioacyl” is intended to mean a —C(S)—R radical, where R is a substituted or unsubstituted alkyl, cycloalkyl, aryl, heterocycloalkyl or heteroaryl group. “Sulfonyl” is intended to mean an —SO2— biradical. “Sulfenyl” is intended to mean an —SO— biradical. “Sulfo” is intended to mean an —SO2H radical. “Hydroxy” is intended to mean the radical —OH. “Amine” or “amino” is intended to mean the radical —NH2. “Alkylamino” is intended to mean the radical —NHRa, where Ra is an alkyl group. “Dialkylamino” is intended to mean the radical —NRaRb, where Ra and Rb are each independently an alkyl group, and is intended to include heterocycloalkyl groups, wherein Ra and Rb, taken together, form a heterocyclic ring that includes the amine nitrogen. “Alkoxy” is intended to mean the radical —ORa, where Ra is an alkyl group. Exemplary alkoxy groups include methoxy, ethoxy, propoxy, and the like. “Lower alkoxy” groups have alkyl moieties having from 1 to 4 carbons. “Alkoxycarbonyl” is intended to mean the radical —C(O)ORa, where Ra is an alkyl group. “Alkylsulfonyl” is intended to mean the radical —SO2Ra, where Ra is an alkyl group. “Alkylenedioxy” is intended to mean the divalent radical —ORaO— which is bonded to adjacent atoms (e.g., adjacent atoms on a phenyl or naphthyl ring), wherein Ra is a lower alkyl group. “Alkylaminocarbonyl” is intended to mean the radical —C(O)NHRa, where Ra is an alkyl group. “Dialkylaminocarbonyl” is intended to mean the radical —C(O)NRaRb, where Ra and Rb are each independently an alkyl group. “Mercapto” is intended to mean the radical —SH. “Alkylthio” is intended to mean the radical —SRa, where Ra is an alkyl group. “Carboxy” is intended to mean the radical —C(O)OH. “Keto” or “oxo” is intended to mean the diradical ═O. “Thioketo” is intended to mean the diradical ═S. “Carbamoyl” is intended to mean the radical —C(O)NH2. “Cycloalkylalkyl” is intended to mean the radical-alkyl-cycloalkyl, wherein alkyl and cycloalkyl are defined as above, and is represented by the bonding arrangement present in the groups —CH2-cyclohexane or —CH2-cyclohexene. “Arylalkyl” is intended to mean the radical-alkylaryl, wherein alkyl and aryl are defined as above, and is represented by the bonding arrangement present in a benzyl group. “Aminocarbonylalkyl” is intended to mean the radical-alkylC(O)NH2 and is represented by the bonding arrangement present in the group —CH2CH2C(O)NH2. “Alkylaminocarbonylalkyl” is intended to mean the radical-alkylC(O)NHRa, where Ra is an alkyl group and is represented by the bonding arrangement present in the group —CH2CH2C(O)NHCH3. “Alkylcarbonylaminoalkyl is intended to mean the radical-alkylNHC(O)-alkyl and is represented by the bonding arrangement present in the group —CH2NHC(O)CH3. “Dialkylaminocarbonylalkyl” is intended to mean the radical-alkylC(O)NRaRb, where Ra and Rb are each independently an alkyl group. “Aryloxy” is intended to mean the radical —ORc, where Rc is an aryl group. “Heteroaryloxy” is intended to mean the radical —ORd, where Rd is a heteroaryl group. “Arylthio” is intended to mean the radical —SRc, where Rc is an aryl group. “Heteroarylthio” is intended to mean the radical-Se, where Rd is a heteroaryl group.

[0072] One embodiment of this invention comprises the compounds depicted by Formula I-A:

[0073] wherein:

[0074] R1 is an aliphatic group, a bi- or tri-cyclic carbocyclic or heterocyclic group or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0075] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0076] R2′ is H or a C1-C6 alkyl group;

[0077] or R2 and R2′ taken together with the nitrogen atom to which they are attached form an unsubstituted or substituted carbocyclic or heterocyclic ring;

[0078] X is

[0079] wherein Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group, wherein Rx is H or one or more substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0080] n is 1 or 2;

[0081] R8 and R8′ are each independently H, halo or a C1-C4 aliphatic group;

[0082] Z is S, O, SO, SO2, CH2, CHF, CF2, CH(OH), CH(O—RZ), CH(N—RZRZ′), CH(S—RZ), C(═O), or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group and RZ′ is H or a C1-C6 aliphatic group;

[0083] R3 is H or a C1-C6 aliphatic group;

[0084] R4 and R5 are independently selected from H, halo, a C1-C6 aliphatic group or a group having the formula C(O)R4′, wherein R4′ is an aliphatic, carbocyclic or heterocyclic group;

[0085] R6 and R7 are independently selected from H, halo or a C1-C6 aliphatic group;

[0086] wherein any of said aliphatic groups are unsubstituted or substituted by one or more suitable substituents and saturated, partially unsaturated or fully unsaturated; and

[0087] wherein any of said carbocyclic or heterocyclic groups are mono-, bi- or tri-cyclic; saturated, partially unsaturated or fully unsaturated; or unsubstituted or substituted by one or more suitable substituents.

[0088] provided that R2 is not an aliphatic group, a phenyl group or a phenyl-substituted aliphatic group, when A is absent; Z is S, SO, SO2, CHF, O, or CH2; V is C═O; W is N; R2′, R3, R8 and R8′ are H or a C1-C4 alkyl group; R4, R5, R6 and R7 are H or a C1-C6 alkyl group; X is

[0089] R1 is a substituted or unsubstituted 5 or 6-membered mono-cyclic carbocyclic or heterocyclic group;

[0090] Another embodiment of this invention comprises the compounds depicted by Formula I-A, wherein:

[0091] R1 is a 3-, 4-, or 7-membered mono-cyclic carbocyclic or heterocyclic group.

[0092] In another embodiment, the compounds of this invention are depicted by Formula I-A, wherein:

[0093] R1 is a 5- or 6-membered monocyclic carbocyclic or heterocyclic group; and

[0094] R2 is cycloalkyl, cycloalkylalkyl, cycloalkenyl, cycloalkenylalkyl, a bi- or tri-cyclic carbocyclic group, a bi- or tri-cyclic carbocyclic-alkyl group, a bi- or tri-cyclic carbocyclic-alkenyl group, a bi- or tri-cyclic carbocyclic-alkynyl group, a heterocyclic group, a heterocyclic-alkyl group, a heterocyclic-alkenyl group or a heterocyclic-alkynyl group;

[0095] Another embodiment of this invention relates to compounds useful for inhibiting the activity of HIV-protease having Formula I-A, wherein:

[0096] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0097] X is

[0098] where Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group, n is 0, 1 or 2 and Rx is H or one or more suitable substituents independently selected from C1-C6 alkyl, nitro, amino, cyano, halogen, C1-C6 haloalkyl, hydroxyl, C1-C6 alkoxy, alkylenedioxy, C1-C6 alkylcarbonyl, C1-C6 alkyloxycarbonyl, C1-C6 alkylcarbonyloxy, carboxyl, carbamoyl, formyl, C1-C6 alkylamino, di-C1-C6 alkylamino, C1-C6 alkylaminocarbonyl, di-C1-C4 alkylaminocarbonyl, C1-C6 alkylaminothiocarbonyl, di-C1-C6-alkylaminothiocarbonyl, C1-C6 alkylsulfonyl, C1-C6 alkylsulfenyl, C1-C6 alkylcarbonylamino, C1-C6 alkylthiocarbonylamino, C1-C6 alkylsulfonyloxy, C1-C6 alkylsulfonylamino, mercapto, C1-C6 alkylthio and halo-C1-C6 alkylthio; and

[0099] R8 and R8″ are each independently H, halo or a C1-C4 aliphatic group provided that R8 and R8″ are not both H when X is

[0100] Another embodiment of this invention relates to compounds depicted by Formula I-A, wherein:

[0101] R1 is a bi- or tri-cyclic carbocyclic or heterocyclic group, wherein said carbocyclic or heterocyclic group is saturated, partially unsaturated or fully unsaturated; and unsubstituted or substituted by one or more suitable substitutents.

[0102] A specific embodiment of a compound of Formula I-A of this invention, wherein Z is S and R2′, R8 and R8′ are each H, may be represented as follows:

[0103] wherein the formula variables are as defined in Formula I-A, above.

[0104] Another embodiment of this invention comprises the compounds depicted by Formula I-B:

[0105] wherein

[0106] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0107] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0108] R2′ is H or a C1-C6 aliphatic group;

[0109] X is

[0110] wherein Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group; n is 1 or 2; and Rx is H or one or more suitable substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0111] R8 and R8″ are each independently H, halo or a C1-C4 aliphatic group;

[0112] Z is S, O SO, SO2, CH2, CHF, CF2, CH(OH), CH(O—RZ), CH(N—RZRZ′), CH(S—RZ), C(═O), or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group and RZ′ is H or a C1-C6 aliphatic group;

[0113] R3 is H or a C1-C6 aliphatic group;

[0114] R4 and R5 are independently selected from H, halo, a C1-C6 aliphatic group or a group having the formula C(O)R4′, wherein R4′ is an aliphatic, carbocyclic or heterocyclic group;

[0115] R6 and R7 are independently selected from H, halo or a C1-C6 aliphatic group;

[0116] where any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0117] where any of said carbocyclic or heterocyclic groups are optionally unsubstituted, substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0118] A specific embodiment of a compound of Formula I-B of this invention, wherein Z is S and R2′, R8 and R8′ are each H, may be represented as follows:

[0119] wherein the formula variables are as defined in Formula I-B, above.

[0120] In yet another embodiment, the compounds of this invention useful for inhibiting the activity of HIV-protease have the Formula I-C:

[0121] wherein

[0122] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0123] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0124] W is N, O or C;

[0125] when W is N or C, R2′ is H or a C1-C6 alkyl group or R2 and R2′ taken together with the atom W to which they are attached form an unsubstituted or substituted carbocyclic or heterocyclic ring;

[0126] when W is O, R2′ is absent;

[0127] X is

[0128] wherein Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group; n is 1 or 2; and Rx is H or one or more substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0129] R8 and R8′ are each independently H, halo or a C1-C4 aliphatic group;

[0130] Z is CF2, CH(OH), CH(O—RZ) or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group;

[0131] R3 is H or a C1-C6 aliphatic group;

[0132] R4 and R5 are independently selected from H, halo, a C1-C6 aliphatic group or a group having the formula C(O)R4′, wherein R4′ is an aliphatic, carbocyclic or heterocyclic group;

[0133] R6 and R7 are independently selected from H, halo or a C1-C6 aliphatic group;

[0134] where any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0135] where any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0136] A specific embodiment of a compound of Formula I-C of this invention, wherein Z is CF2 and R8 and R8′ are each H, may be represented as follows:

[0137] wherein the formula variables are as defined in Formula I-C, above.

[0138] Another embodiment of this invention comprises the compounds depicted by the Formula I-D, as follows:

[0139] wherein

[0140] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0141] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0142] W is N, O or C;

[0143] when W is N or C, R2′ is H or a C1-C6 alkyl group or R2 and R2′ taken together with the atom W to which they are attached form an unsubstituted or substituted carbocyclic or heterocyclic ring;

[0144] when W is O, R2′ is absent;

[0145] X is

[0146] wherein Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group; n is 1 or 2; and Rx is H or one or more suitable substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0147] R8 and R8′ are each independently H, halo or a C1-C4 aliphatic group;

[0148] Z is S, O, SO, SO2, CHF, CH2, CF2, CH(OH), CH(O—RZ), CH(N—RZRZ′), CH(S—RZ), C(═O), or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group and RZ′ is H or a C1-C6 aliphatic group;

[0149] R3 is H or a C1-C6 aliphatic group;

[0150] R4 and R5 are independently selected from H, halo, a C1-C6 aliphatic group or a group having the formula C(O)R4′, wherein R4′ is an aliphatic, carbocyclic or heterocyclic group;

[0151] R6 and R7 are independently selected from H, halo or a C1-C6 aliphatic group;

[0152] where any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0153] where any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0154] Another embodiment of this invention comprises the compounds depicted by the Formula I-E, as follows:

[0155] wherein

[0156] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0157] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0158] W is N, O or C;

[0159] when W is N or C, R2′ is H or a C1-C6 alkyl group or R2 and R2′ taken together with the atom W to which they are attached form an unsubstituted or substituted carbocyclic or heterocyclic ring;

[0160] when W is O, R2′ is absent;

[0161] X is

[0162] wherein Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group, wherein Rx is H or one or more suitable substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, alkylthio;

[0163] R8 and R8′ are each independently H, halo or a C1-C4 aliphatic group;

[0164] Z is S, O, SO, SO2, CH2, CHF, CF2, CH(OH), CH(O—RZ), CH(N—RZRZ′), CH(S—RZ), C(═O), or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group and RZ′ is H or a C1-C6 aliphatic group;

[0165] n is 1 or 2;

[0166] R3 is H or a C1-C6 aliphatic group;

[0167] R4 is selected from H, halo, a C1-C6 aliphatic group or a group having the formula C(O)R4′, wherein R4′ is an aliphatic, carbocyclic or heterocyclic group;

[0168] R7 is H, halo or a C1-C6 aliphatic group;

[0169] where any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0170] where any of said carbocyclic or heterocyclic groups are unsubstituted, substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0171] A specific embodiment of s compound of Formula I-E, wherein n is 2 and R8 and R8′ are each H, may be represented as follows:

[0172] wherein the formula variables are as defined above.

[0173] Another embodiment of this invention comprises the compounds of Formula I, wherein A is CH(RA), Z is CH(RZ) and RA and RZ taken together form a 5 or 6-membered carbocyclic ring, depicted by the Formula I-F, as follows:

[0174] wherein

[0175] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0176] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0177] W is N, O or C;

[0178] when W is N or C, R2′ is H or a C1-C6 alkyl group or R2 and R2′ taken together with the atom W to which they are attached form an unsubstituted or substituted carbocyclic or heterocyclic ring;

[0179] when W is O, R2′ is absent;

[0180] X is

[0181] wherein Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group, wherein IX is H or one or more substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0182] n is 1 or 2;

[0183] R3 is H or a C1-C6 aliphatic group;

[0184] R4 and R5 are independently selected from H, halo, a C1-C6 aliphatic group or a group having the formula C(O)R4′, wherein R4′ is an aliphatic, carbocyclic or heterocyclic group;

[0185] R6 and R7 are independently selected from H, halo or a C1-C6 aliphatic group;

[0186] R8 and R8′ are each independently H, halo or a C1-C4 aliphatic group;

[0187] where any of said aliphatic groups ar saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0188] where any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0189] A specific embodiment of a compound of Formula I-F, wherein n is 2 and R8 and R8′ are each H, may be represented as follows:

[0190] wherein the formula variables are as defined above.

[0191] In one embodiment, the compounds of Formula I-A of this invention, wherein R6 and R7, taken together with the atom to which they are bound, form a carbocyclic group, comprise spiro-fused bi-cyclic compounds having the Formula I-G:

[0192] wherein

[0193] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an aliphatic, carbocyclic or heterocyclic group, and R1″ is H or a C1-C6 aliphatic group or R1′ and R1′ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0194] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0195] W is N, O or C;

[0196] when W is N or C, R2′ is H or a C1-C6 alkyl group or R2 and R2′ taken together with the atom W to which they are attached form an unsubstituted or substituted carbocyclic or heterocyclic ring.

[0197] when W is O, R2′ is absent;

[0198] X is

[0199] wherein Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group, wherein Rx is H or one or more substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, alkylthio;

[0200] R8 and R8″ are each independently H, halo or a C1-C4 aliphatic group;

[0201] Z is S, O, SO, SO2, CHF, CH2, CF2, CH(OH), CH(O—RZ), CH(N—RZRZ′), CH(S—RZ), C(═O), or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group and RZ′ is H or a C1-C6 aliphatic group;

[0202] n is 1, 2, 3 or 4;

[0203] R3 is H or a C1-C6 aliphatic group;

[0204] R4 and R5 are independently selected from H, halo, a C1-C6 aliphatic group or a group having the formula C(O)R4, wherein R4′ is an aliphatic, carbocyclic or heterocyclic group;

[0205] where any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0206] where any of said carbocyclic or heterocyclic groups are unsubstituted, substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0207] In the compounds of this inventions, R2 may consist of a substituted aliphatic group; wherein R2 may be represented as —CH2—B, —CH2CH2—B, —CH(CH3)B, and the like, wherein B is a carbocyclic or heterocyclic group as described herein, and wherein the B group may be unsubstituted or substituted with one or more substituents selected from C1-C4 alkyl, halo, haloalkyl, hydroxy, alkoxy, halo alkoxy, alkylthio, haloalkylthio, amino, dialkylamino, alkyl-SO2, cyano, alkylcarbonylamino and cycloalkylalkyloxy.

[0208] Specific embodiments of the compounds of this invention comprise the compounds depicted by Formula I-A′:

[0209] wherein:

[0210] R1 is an alkyl, alkenyl, or alkynyl group, a bi- or tri-cyclic cycloalkyl, cycloalkenyl, aryl, heterocycloalkyl, heterocycloalkenyl or heteroaryl group or a group having the formula: OR1′, SR1′, NHR1′, N(R1′)R1″ or C(O)R1′, wherein R1′ is an alkyl, alkenyl, or alkynyl group, a bi- or tri-cyclic cycloalkyl, cycloalkenyl, aryl, heterocycloalkyl, heterocycloalkenyl or heteroaryl group, or a cycloalkylalkyl, cycloalkenylalkyl, arylalkyl, heterocycloalkylalkyl, heterocycloalkenylalkyl, heteroarylalkyl, cycloalkylalkenyl, cycloalkenylalkenyl, arylalkenyl, heterocycloalkylalkenyl, heterocycloalkenylalkenyl, heteroarylalkenyl, cycloalkylalkynyl, cycloalkenylalkynyl, arylalkynyl, heterocycloalkylalkynyl, heterocycloalkenylalkynyl, or heteroarylalkynyl group; and R1″ is H or a C1-C6 alkyl, alkenyl or alkynyl group or R1′ and R1″ together with the atom to which they are attached form a substituted or unsubstituted heterocyclic ring;

[0211] R2 is a cycloalkyl, cycloalkylalkyl, cycloalkenyl, or cycloalkenylalkyl group, a bi- or tri-cyclic aryl group, a bi- or tri-cyclic arylalkyl group, a bi- or tri-cyclic arylalkenyl group, a bi- or tri-cyclic arylalkynyl group, or a heterocycloalkyl, heterocycloalkylalkyl, heterocycloalkenyl, heterocycloalkenylalkyl, heteroaryl or heteroarylalkyl group;

[0212] R2′ is H or a C1-C6 alkyl group;

[0213] or R2 and R2′ taken together with the nitrogen atom to which they are attached form a heterocycloalkyl or heterocycloalkenyl ring;

[0214] X is

[0215] wherein Y′ and Y″ are independently selected from H, halo, or a C1-C6 aliphatic group, wherein Rx is H or one or more substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0216] Z is S, O, SO, SO2, CH2, CHF, CF2, CH(OH), CH(O—RZ), CH(N—RZRZ′), CH(S—RZ), C(═O), or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group and RZ′ is H or a C1-C6 aliphatic group;

[0217] R3 is H or a C1-C6 aliphatic group;

[0218] R4 and R5 are independently selected from H, halo, and a C1-C6 aliphatic group;

[0219] R6 and R7 are independently selected from H, halo and a C1-C6 aliphatic group;

[0220] where any of the alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heterocycloalkyl, heterocycloalkenyl or heteroaryl groups or the alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heterocycloalkyl, heterocycloalkenyl or heteroaryl moieties of the cycloalkylalkyl, cycloalkenylalkyl, arylalkyl, heterocycloalkylalkyl, heterocycloalkenylalkyl, heteroarylalkyl, cycloalkylalkenyl, cycloalkenylalkenyl, arylalkenyl, heterocycloalkylalkenyl, heterocycloalkenylalkenyl, heteroarylalkenyl, cycloalkylalkynyl, cycloalkenylalkynyl, arylalkynyl, heterocycloalkylalkynyl, and heterocycloalkenylalkynyl, heteroarylalkynyl groups are unsubstituted or substituted by one or more suitable substituents; and

[0221] where any of said carbocyclic or heterocyclic groups are optionally mono-, bi- or tri-cyclic; saturated, partially unsaturated or fully unsaturated; and unsubstituted or substituted by one or more suitable substituents.

[0222] provided that R2 is not an aliphatic group, a phenyl group or a phenyl-substituted aliphatic group, when Z is S, SO, SO2, CHF, O, or CH2; R2′, R3, R8 and R8″ are H or a C1-C4 alkyl group; R4, R5, R6 and R7 are H or a C1-C6 alkyl group; X is

[0223] R1 is a substituted or unsubstituted 5 or 6-membered mono-cyclic carbocyclic or heterocyclic group;

[0224] or provided that R2 is not t-butyl when R1 is substituted or unsubstituted phenyloxymethylene, or quinolylmethylenecarbonylaminomethylene; A is absent; Z is S; R2′, R3, R4, and R5, are H; R6 and R7 are H, methyl, ethyl or propyl; and X is

[0225] wherein Rx is H or methoxy,

[0226] In another embodiment, the compounds of this invention are depicted by Formula I-A; wherein:

[0227] Z is CF2, CH(OH), CH(O—Rz), CH(NRzRz′), CH(S—Rz), C═O or CH(Rz), where Rz is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group and Rz′ is H or a C1-C6 aliphatic group.

[0228] Specific examples of the compounds of Formula I-B comprise compounds having the formula I-B′

[0229] wherein

[0230] R1 is an aliphatic, carbocyclic or heterocyclic group,

[0231] R2 is an aliphatic group, a carbocyclic-aliphatic group, or a heterocyclic-aliphatic group;

[0232] R2′ is H or a C1-C6 alkyl group;

[0233] or R2 and R2′ taken together with the carbon atom to which they are both attached form an unsubstituted or substituted carbocyclic ring;

[0234] X is

[0235] wherein Rx is H or one or more substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0236] Z is S, O, SO, SO2, CHF, CH2, CF2, C(═O), or CH(RZ), where RZ is a C1-C6 aliphatic group or a carbocyclic or heterocyclic group;

[0237] R3 is H or a C1-C6 aliphatic group;

[0238] R4 and R5 are independently selected from H, halo, or a C1-C6 aliphatic group;

[0239] R6 and R7 are independently selected from H, halo or a C1-C6 aliphatic group;

[0240] wherein any of said aliphatic groups are saturated, partially saturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0241] wherein any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0242] More specific examples of the compounds of Formula I-B′ comprise compounds wherein

[0243] R1 is a carbocyclic group,

[0244] R2 is a C1-C6 aliphatic group or a carbocyclic-C1-C6-aliphatic group;

[0245] Z is S, O, CH2, CF2;

[0246] R3, R4 and R5 are each H; and

[0247] R6 and R7 are each a C1-C6 aliphatic group;

[0248] where any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0249] where any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0250] Specific examples of the compounds of Formula I-B′ comprise compounds wherein

[0251] R1 is a phenyl group, unsubstituted or substituted with one or more substituents selected from alkyl, hydroxyl, halo, halo alkyl, haloalkoxy, methylene dioxy, and di-fluoromethylene dioxy;

[0252] R2 is an alkenyl group, an aralkyl group or a straight or branched chain saturated alkyl;

[0253] X is

[0254] where Rx is H;

[0255] Z is S;

[0256] R3, R4 and R5 are each H; and

[0257] R6 and R7 are each methyl;

[0258] wherein any of said alkenyl, aralkyl, or alkyl groups are unsubstituted or substituted with one or more substituents, independently selected from methyl, halo, trifluoromethyl or methoxy.

[0259] Another specific emobdiment of the compounds of Formula I-B′ comprise compounds wherein

[0260] R1 is a phenyl group, unsubstituted or substituted with one or more substituents selected from alkyl, hydroxyl, halo, halo alkyl, haloalkoxy, methylene dioxy, and di-fluoromethylene dioxy;

[0261] R2 is an alkenyl group, an aralkyl group or a straight or branched chain saturated alkyl;

[0262] X is

[0263] where Rx is H;

[0264] Z is CF2;

[0265] R3, R4 and R5 are each H; and

[0266] R6 and R7 are each methyl;

[0267] Wherein any of said alkenyl, aralkyl, or alkyl groups are unsbstituted or substituted with one or more substitutents, independently selected from methyl, halo, trifluoromethyl or methoxy.

[0268] Other specific examples of this invention, comprise the compounds having the Formula I-C:

[0269] wherein

[0270] R1 is an aliphatic, carbocyclic or heterocyclic group, or a group having the formula: OR1′, wherein R1′ is a carbocyclic or heterocyclic group;

[0271] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0272] W is N;

[0273] R2′ is H or a C1-C6 alkyl group;

[0274] X is

[0275] wherein Rx is H; dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, or alkylthio;

[0276] Z is CF2, CH(OH) or C(═O);

[0277] R3, R4 and R5 are each H; and

[0278] R6 and R7 are each methyl.

[0279] More specific examples of this invention, comprise the compounds having the Formula I-C′, wherein:

[0280] R1 is an aryl group, an aryloxyalkyl group, an alkynyloxy group, a heterocycloalkyloxy group or heteroaryl group;

[0281] R2 is an alkyl, alkenyl, or alkynyl group, an arylalkyl group; a heteroarylalkyl group, an indanyl group, a chromanyl group, a tetrahydronaphthalene group, an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group; and

[0282] R2′ is H;

[0283] wherein the alkyl, alkenyl, alkynyl, arylalkyl; heteroarylalkyl, indanyl, chromanyl or tetrahydronaphthalene group is optionaaly unsubstituted or substitutee with one or more substituents independently selected from alkyl, hydroxy, halo, haloalkyl, cyano, alkoxy or methylenedioxy.

[0284] Specific examples of this invention, comprise the compounds having the Formula I-C′, wherein:

[0285] R1 is a phenyl group, a phenyoxymethyl group, a tetrahydrofuranyloxy group, a C1-C4 alkynyloxy group, or a isoxazolyl group, where the phenyl group, phenyoxymethyl group or isoxazolyl group is unsubstituted or substituted by hydroxyl or methyl;

[0286] R2 is an C1-C5 alkyl, C1-C6 alkenyl, or C1-C4 alkynyl group, a benzyl group; a furanylmethyl group, a thienylmehtyl group, an indanyl group, a chromanyl group, a tetrahydronaphthalene group, or a cyclohexenyl group, where the alkyl groups is unsubstituted or substituted with one or more halogen; and the phenyl group is unsubstituted or substituted with halogen, hydroxyl, methoxy, methylenedioxy or methyl;

[0287] R2′ is H;

[0288] X is

[0289] wherein Rx is H; and

[0290] Z is CF2;

[0291] Other specific embodiments of this invention comprise the compounds depicted by the Formula I-D′ or I-E′, as follows:

[0292] wherein

[0293] R1 is a carbocyclic or heterocyclic group,

[0294] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0295] W is N;

[0296] R2′ is H or a C1-C6 alkyl group;

[0297] X is

[0298] wherein Rx is H or one or more substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0299] Z is O, CH2, CHF, CF2, or CH(RZ), where RZ is a C1-C6 aliphatic group;

[0300] R3, R4, R5, R6 and R7 are each H; and

[0301] wherein any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0302] wherein any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0303] More specifically, embodiments of this invention, comprise compounds according to Formula I-D′ or I-E′ wherein

[0304] R1 is a carbocyclic group;

[0305] R2 is an arylalkyl group;

[0306] R2′ is H;

[0307] X is

[0308] wherein Rx is H; and

[0309] Z is CH2;

[0310] wherein said carbocyclic group and arylalkyl group are unsubstituted or substituted with one or more substituents selected from methyl, halo, or hydroxy.

[0311] Another specific embodiment of this invention comprises compounds of Formula I-F′, as follows:

[0312] wherein

[0313] R1 is a carbocyclic or heterocyclic group,

[0314] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0315] W is N;

[0316] R2′ is H or a C1-C6 alkyl group;

[0317] X is

[0318] wherein Rx is H or one or more substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0319] n is 1 or 2;

[0320] R3, R4 and R5 are each H; and

[0321] R7 is H;

[0322] wherein any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0323] wherein any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0324] More specifically, embodiments of this invention, comprise compounds according to Formula I-F′, wherein

[0325] R1 is a carbocyclic group;

[0326] R2 is an arylalkyl group;

[0327] R2′ is H;

[0328] X is

[0329] wherein Rx is H;

[0330] wherein said carbocyclic group, and arylalkyl group unsubstituted or substituted with one or more substituents selected from methyl, halo, or hydroxy.

[0331] In one embodiment, the compounds of Formula I-A of this invention, wherein R6 and R7, taken together with the atom to which they are bound, form a carbocyclic group, comprise spiro-fused bi-cyclic compounds having the Formula I-G′:

[0332] wherein

[0333] R1 is a carbocyclic or heterocyclic group;

[0334] R2 is an aliphatic group, a carbocyclic group, a carbocyclic-aliphatic group, a heterocyclic group, or a heterocyclic-aliphatic group;

[0335] W is N, C or CH;

[0336] R2′ is H

[0337] X is

[0338] wherein Rx is H or one or more suitable substituents independently selected from alkyl, nitro, amino, cyano, halogen, haloalkyl, hydroxyl, alkoxy, alkylenedioxy, alkylcarbonyl, alkyloxycarbonyl, alkylcarbonyloxy, carboxyl, carbamoyl, formyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, alkylsulfonyl, alkylsulfenyl, alkylcarbonylamino, alkylthiocarbonylamino, alkylsulfonyloxy, alkylsulfonylamino, mercapto, and alkylthio;

[0339] Z is S, O, CH2, CHF, CF2, or CH(RZ), where RZ is a C1-C6 aliphatic group;

[0340] n is 2, 3 or 4;

[0341] R3, R4 and R5 are each H;

[0342] wherein any of said aliphatic groups are saturated, partially unsaturated or fully unsaturated and unsubstituted or substituted by one or more suitable substituents; and

[0343] wherein any of said carbocyclic or heterocyclic groups are unsubstituted or substituted by one or more suitable substituents; saturated, partially unsaturated or fully unsaturated; or mono-, bi- or tri-cyclic.

[0344] More specific embodiments comprise the compounds of Formula I-G′ wherein:

[0345] R1 is a carbocyclic group;

[0346] R2 is an arylalkyl group;

[0347] W is N;

[0348] R2′ is H;

[0349] X is

[0350] wherein Rx is H; and

[0351] Z is CH2;

[0352] R3, R4, R and R7 are each H;

[0353] wherein said carbocyclic group and arylalkyl group unsubstituted or substituted with one or more substituents selected from methyl, halo, or hydroxy.

[0354] More specific embodiments comprise the compounds of Formula I-G′ wherein:

[0355] R1 is a carbocyclic group;

[0356] R2 is an arylalkyl group;

[0357] W is N;

[0358] R2′ is H;

[0359] X is

[0360] wherein Rx is H; and

[0361] Z is CF2;

[0362] R3, R4, R5 and R7 are each H;

[0363] wherein said carbocyclic group and arylalkyl group unsubstituted or substituted with one or more substituents selected from methyl, halo, or hydroxy.

[0364] More specific embodiments comprise the compounds of Formula I-G′ wherein:

[0365] R1 is a carbocyclic group;

[0366] R2 is an arylalkyl group;

[0367] W is N;

[0368] R2′ is H;

[0369] X is

[0370] wherein Rx is H; and

[0371] Z is S;

[0372] R3, R4, R5 and R7 are each H;

[0373] wherein said carbocyclic group and arylalkyl group unsubstituted or substituted with one or more substituents selected from methyl, halo, or hydroxy.

[0374] If an inventive compound is a base, a desired salt may be prepared by any suitable method known in the art, including treatment of the free base with an inorganic acid, such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like, or with an organic acid, such as acetic acid, maleic acid, succinic acid, mandelic acid, fumaric acid, malonic acid, pyruvic acid, oxalic acid, glycolic acid, salicylic acid, pyranosidyl acid, such as glucuronic acid or galacturonic acid, alpha-hydroxy acid, such as citric acid or tartaric acid, amino acid, such as aspartic acid or glutamic acid, aromatic acid, such as benzoic acid or cinnamic acid, sulfonic acid, such as p-toluenesulfonic acid or ethanesulfonic acid, or the like.

[0375] If an inventive compound is an acid, a desired salt may be prepared by any suitable method known to the art, including treatment of the free acid with an inorganic or organic base, such as an amine (primary, secondary, or tertiary); an alkali metal or alkaline earth metal hydroxide; or the like. Illustrative examples of suitable salts include organic salts derived from amino acids such as glycine and arginine; ammonia; primary, secondary, and tertiary amines; and cyclic amines, such as piperidine, morpholine, and piperazine; as well as inorganic salts derived from sodium, calcium, potassium, magnesium, manganese, iron, copper, zinc, aluminum, and lithium.

[0376] All compounds of this invention contain at least one chiral center and may exist as single stereoisomers (e.g., single enantiomers or single diastereomers), any mixture of stereosisomers (e.g., any mixture of enantiomers or diastereomers) or racemic mixtures thereof. All such single stereoisomers, mixtures and racemates are intended to be encompassed within the broad scope of the present invention. Compounds identified herein as single stereoisomers are meant to describe compounds that are present in a form that contains at least 90% of a single stereoisomer of each chiral center present in the compounds. Where the stereochemistry of the chiral carbons present in the chemical structures illustrated herein is not specified, the chemical structure is intended to encompass compounds containing either stereoisomer of each chiral center present in the compound. Preferably, however, the inventive compounds are used in optically pure, that is, stereoisomerically pure, form or substantially optically pure (substantially stereoisomerically pure) form. As used herein, the term “stereoisomeric” purity (or “optical” purity) refers to the “enantiomeric” purity and/or “diastereomeric” purity of a compound. Compounds that are substantially enantiomerically pure contain at least 90% of a single isomer and preferably contain at least 95% of a single isomer of each chiral center present in the enantiomer. Compounds that are substantially diastereomerically pure contain at least 90% of a single isomer of each chiral center present in the diastereomer, and preferably contain at least 95% of a single isomer of each chiral center. More preferably, the substantially enantiomerically and diasteriomerically pure compounds in this invention contain at least 97.5% of a single isomer and most preferably contain at least 99% of a single isomer of each chiral center in the compound. The term “racemic” or “racemic mixture” refers to a mixture of equal amounts of enantiomeric compounds, which encompasses mixtures of enantiomers and mixtures of enantiomeric diastereomers. The compounds of this invention may be obtained in stereoisomerically pure (i.e., enantiomerically and/or diastereomerically pure) or substantially stereoisomerically pure (i.e., substantially enantiomerically and/or diastereomerically pure) form. Such compounds may be obtained synthetically, according to the procedures described herein using optically pure or substantially optically pure materials. Alternatively, these compounds may be obtained by resolution/separation of a mixture of stereoisomers, including racemic mixtures, using conventional procedures. Exemplary methods that may be useful for the resolution/separation of stereoisomeric mixtures include chromatography and crystallization/re-crystallization. Other useful methods may be found in “Enantiomers, Racemates, and Resolutions,” J. Jacques et al., 1981, John Wiley and Sons, New York, N.Y., the disclosure of which is incorporated herein by reference. Preferred stereoisomers of the compounds of this invention are described herein.

[0377] Especially preferred embodiments of this invention comprise compounds, wherein the stereogenic centers (chiral carbons) have the following designated stereochemistry:

[0378] More preferably, at least two of the stereogenic centers have the following designated stereochemistry:

[0379] Even more preferably, at least three of the stereogenic centers have the following designated stereochemistry:

[0380] Exemplary compounds of this invention may be represented as follows:

[0381] wherein each of the formula variables are as defined above.

[0382] Exemplary compounds of this invention include the following. The abbreviation “Bn” in some of the following structures indicates a “benzyl” substituent.

[0383] and the prodrugs, pharmaceutically active metabolites, and pharmaceutically acceptable salts and solvates thereof.

[0384] The invention is also directed to the intermediates of Formula II, which are useful in the synthesis of certain compounds of Formula I:

[0385] The HIV protease inhibitor compounds of this invention include prodrugs, the pharmaceutically active metabolites, and the pharmaceutically acceptable salts and solvates thereof. In preferred embodiments, the compounds of Formula I, prodrugs, pharmaceutically acceptable salts, and pharmaceutically active metabolites and solvates thereof demonstrate an HIV-protease inhibitory activity, corresponding to Ki of at least 100 nM, an EC50 of at least 10 mM or an IC50 of at least 10 mM. Preferably, the compounds of this invention demonstrate an HIV-protease inhibitory activity, corresponding to a Ki of at least 10 nM, an EC50 of at least 1 mM or an IC50 of at least 1 mM. More preferably, the compounds of this invention demonstrate an HIV-protease inhibitory activity against mutant strains of HIV, corresponding to a Ki of at least 100 nM, an EC50 of at least 10 mM or an IC50 of at least 10 mM. Even more preferably, the compounds of this invention demonstrate protease inhibitory activity against mutant strains corresponding to a Ki of at least 10 nM, an EC50 of at least 1 mM or an IC50 of at least 1 mM.

[0386] A “prodrug” is intended to mean a compound that is converted under physiological conditions or by solvolysis or metabolically to a specified compound that is pharmaceutically active. A prodrug may be a derivative of one of the compounds of this invention that contains a moiety, such as for example —CO2R, —PO(OR)2 or —C═NR, that may be cleaved under physiological conditions or by solvolysis. Any suitable R substituent may be used that provides a pharmaceutically acceptable solvolysis or cleavage product. A prodrug containing such a moiety may be prepared according to conventional procedures by treatment of a compound of this invention containing, for example, an amido, carboxylic acid, or hydroxyl moiety with a suitable reagent. A “pharmaceutically active metabolite” is intended to mean a pharmacologically active compound produced through metabolism in the body of a specified compound. Prodrugs and active metabolites of compounds of this invention of the above-described Formulas may be determined using techniques known in the art, for example, through metabolic studies. See, e.g., “Design of Prodrugs,” (Bundgaard, ed.), 1985, Elsevier Publishers B.V., Amsterdam, The Netherlands. The following are examples of prodrugs that can be converted to the compounds of this invention under physiological conditions, by solvolysis or metabolically:

[0387] A “pharmaceutically acceptable salt” is intended to mean a salt that retains the biological effectiveness of the free acids and bases of a specified compound and that is not biologically or otherwise undesirable. Examples of pharmaceutically acceptable salts include sulfates, pyrosulfates, bisulfates, sulfites, bisulfites, phosphates, monohydrogenphosphates, dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides, bromides, iodides, acetates, propionates, decanoates, caprylates, acrylates, formates, isobutyrates, caproates, heptanoates, propiolates, oxalates, malonates, succinates, suberates, sebacates, fumarates, maleates, butyne-1,4-dioates, hexyne-1,6-dioates, benzoates, chlorobenzoates, methylbenzoates, dinitrobenzoates, hydroxybenzoates, methoxybenzoates, phthalates, sulfonates, xylenesulfonates, phenylacetates, phenylpropionates, phenylbutyrates, citrates, lactates, γ-hydroxybutyrates, glycollates, tartrates, methane-sulfonates (mesylates), propanesulfonates, naphthalene-1-sulfonates, naphthalene-2-sulfonates, and mandelates. A “solvate” is intended to mean a pharmaceutically acceptable solvate form of a specified compound that retains the biological effectiveness of such compound. Examples of solvates include compounds of the invention in combination with water, isopropanol, ethanol, methanol, DMSO, ethyl acetate, acetic acid, or ethanolamine. In the case of compounds, salts, or solvates that are solids, it is understood by those skilled in the art that the inventive compounds, salts, and solvates may exist in different crystal forms, all of which are intended to be within the scope of the present invention and specified formulas.

[0388] The present invention is also directed to a method of inhibiting HIV protease activity, comprising contacting the protease with an effective amount of a compound of Formula I, or a pharmaceutically acceptable salt, prodrug, pharmaceutically active metabolite, or solvate thereof. For example, HIV protease activity may be inhibited in mammalian tissue by administering a compound of Formula I or a pharmaceutically acceptable salt, prodrug, pharmaceutically active metabolite, or solvate thereof. More preferably, the present method is directed at inhibiting HIV-protease activity. “Treating” or “treatment” is intended to mean at least the mitigation of a disease condition in a mammal, such as a human, that is alleviated by the inhibition of the activity of HIV proteases. The methods of treatment for mitigation of a disease condition include the use of the compounds in this invention in any conventionally acceptable manner, for example, as a prophylactic. The activity of the inventive compounds as inhibitors of HIV protease activity may be measured by any of the suitable methods known to those skilled in the art, including in vivo and in vitro assays. Examples of suitable assays for activity measurements are escribed herein. Administration of the compounds of the Formula I and their pharmaceutically acceptable prodrugs, salts, active metabolites, and solvates may be performed according to any of the generally accepted modes of administration available to those skilled in the art. Illustrative examples of suitable modes of administration include oral, nasal, parenteral, topical, transdermal, and rectal.

[0389] An inventive compound of Formula I or a pharmaceutically acceptable salt, prodrug, active metabolite, or solvate thereof may be administered as a pharmaceutical composition in any pharmaceutical form recognizable to the skilled artisan as being suitable. Suitable pharmaceutical forms include solid, semisolid, liquid, or lyophilized formulations, such as tablets, powders, capsules, suppositories, suspensions, liposomes, and aerosols. Pharmaceutical compositions of the invention may also include suitable excipients, diluents, vehicles, and carriers, as well as other pharmaceutically active agents, depending upon the intended use or mode of administration. Acceptable methods of preparing suitable pharmaceutical forms of the pharmaceutical compositions may be routinely determined by those skilled in the art. For example, pharmaceutical preparations may be prepared following conventional techniques of the pharmaceutical chemist involving steps such as mixing, granulating, and compressing when necessary for tablet forms, or mixing, filling, and dissolving the ingredients as appropriate, to give the desired products for oral, parenteral, topical, intravaginal, intranasal, intrabronchial, intraocular, intraaural, and/or rectal administration.

[0390] The present invention includes pharmaceutical compositions useful for inhibiting HIV protease, comprising an effective amount of a compound of this invention, and a pharmaceutically acceptable carrier. Pharmaceutical compositions useful for treating infection by HIV, or for treating AIDS or ARC, are also encompassed by the present invention, as well as a method of inhibiting HIV protease, and a method of treating infection by HIV, or of treating AIDS or ARC. Additionally, the present invention is directed to a pharmaceutical composition comprising a therapeutically effective amount of a compound of the present invention in combination with a therapeutically effective amount of an HIV infection/AIDS treatment agent selected from:

[0391] 1) an HIV/AIDS antiviral agent,

[0392] 2) an anti-infective agent, and

[0393] 3) an immunomodulator.

[0394] The present invention also includes the use of a compound of the present invention as described above in the preparation of a medicament for (a) inhibiting HIV protease, (b) preventing or treating infection by HIV, or (c) treating AIDS or ARC.

[0395] The present invention further includes the use of any of the HIV protease inhibiting compounds of the present invention as described above in combination with one or more HIV infection/AIDS treatment agents selected from an HIV/AIDS antiviral agent, an anti-infective agent, and an immunomodulator for the manufacture of a medicament for (a) inhibiting HIV protease, (b) preventing or treating infection by HIV, or (c) treating AIDS or ARC, said medicament comprising an effective amount of the HIV protease inhibitor compound and an effective amount of the one or more treatment agents.

[0396] Solid or liquid pharmaceutically acceptable carriers, diluents, vehicles, or excipients may be employed in the pharmaceutical compositions. Illustrative solid carriers include starch, lactose, calcium sulfate dihydrate, terra alba, sucrose, talc, gelatin, pectin, acacia, magnesium stearate, and stearic acid. Illustrative liquid carriers include syrup, peanut oil, olive oil, saline solution, and water. The carrier or diluent may include a suitable prolonged-release material, such as glyceryl monostearate or glyceryl distearate, alone or with a wax. When a liquid carrier is used, the preparation may be in the form of a syrup, elixir, emulsion, soft gelatin capsule, sterile injectable liquid (e.g., solution), or a nonaqueous or aqueous liquid suspension. A dose of the pharmaceutical composition contains at least a therapeutically effective amount of the active compound (i.e., a compound of Formula I or a pharmaceutically acceptable salt, prodrug, active metabolite, or solvate thereof), and preferably is made up of one or more pharmaceutical dosage units. The selected dose may be administered to a mammal, for example, a human patient, in need of treatment mediated by inhibition of HIV protease activity, by any known or suitable method of administering the dose, including: topically, for example, as an ointment or cream; orally; rectally, for example, as a suppository; parenterally by injection; or continuously by intravaginal, intranasal, intrabronchial, intraaural, or intraocular infusion. A “therapeutically effective amount” is intended to mean the amount of an inventive agent that, when administered to a mammal in need thereof, is sufficient to effect treatment for disease conditions alleviated by the inhibition of the activity of one or more variant of the HIV protease. The amount of a given compound of the invention that will be therapeutically effective will vary depending upon factors such as the particular compound, the disease condition and the severity thereof, the identity of the mammal in need thereof, which amount may be routinely determined by artisans.

[0397] The compounds of this invention are also useful in the preparation and execution of screening assays for antiviral compounds. For example, the compounds of this invention are useful for isolating enzyme mutants that are excellent screening tools for more powerful antiviral compounds. Furthermore, the compounds of this invention are useful in establishing or determining the binding site of other antivirals to HIV protease, e.g., by competitive inhibition. Thus the compounds of this invention are commercial products to be sold for these purposes.

General Synthetic Methods

[0398] Preferably, the inventive compounds are prepared by the methods of the present invention, including the General Methods shown below. When stereochemistry is not specified in chemical structures, either stereocenter may be utilized. The following abbreviations also apply: Boc (tert-butoxycarbonyl), Ac (acetyl), Cbz (benzyloxycarbonyl), DMB (2,4-dimethoxybenzyl), TBS (tert-butyldimethylsilyl), TBDPS (tert-butyldiphenylsilyl), Ms (methanesulfonate), Ts (toluenesulfonate), Bn (benzyl), and Tr (triphenylmethyl)

[0399] All reactions were performed in septum-sealed flasks under a slight positive pressure of argon unless otherwise noted. All commercial reagents and solvents were used as received from their respective suppliers with the following exceptions: Tetrahydrofuran (THF) was distilled from sodium benzophenone ketyl prior to use. Dichloromethane (CH2Cl2) was distilled from calcium hydride prior to use. Flash chromatography was performed using silica gel 60 (Merck art. 9385). 1H NMR spectra were recorded at 300 MHz utilizing a Varian UNITYplus 300 spectrometer. Chemical shifts are reported in ppm (6) downfield relative to internal tetramethylsilane, and coupling constants are given in Hertz. Infrared absorption spectra were recorded using a Perkin-Elmer 1600 series FTIR spectrometer. Elemental analyses were performed by Atlantic Microlab, Inc., Norcross, Ga. Melting points are uncorrected.

[0400] All P2′ amine variants mentioned in General Methods A-E described hereinbelow were either purchased and used directly or synthesized as follows.

[0401] Method A: Representative Procedure for Reduction of Ketones to Alcohols.

[0402] 6,7-Dihydro-4-(5H)-benzofuranone (1) (1.00 g 7.34 mmol) was dissolved in methanol (55 mL). The mixture was cooled to 0° C. and NaBH4 (0.31 g, 8.08 mmol) was added in portions. The reaction was stirred for 2 h at 0° C. at which time the methanol was evaporated. The residue was dissolved in EtOAc and poured into NaHCO3 (saturated aqueous) and extracted with EtOAc (3×10 mL). The combined organic extracts were washed with brine (10 mL), passed over a short plug of Na2SO4, and concentrated in vacuo to give 2 (1.01 g, 99%, as a mixture of isomers) as a pale yellow, thick oil, which was of sufficient quality to be advanced to the next step without further purification. Rf (50% EtOAc/hexanes): 0.53.

[0403] Method B: Representative Procedure for Reduction of Acids to Alcohols.

[0404] Tiglic acid (1) (20.0 g, 0.200 mol) was dissolved in ether (80 ml) and added dropwise over 30 min to a suspension of LiAlH4 (15.0 g, 0.417 mol) in ether (80 ml) at 0° C. and the reaction mixture was allowed to warm to room temperature. After 3 h the mixture was re-cooled to 0° C. and quenched slowly by the addition of H2O (15 ml), 15% NaOH (15 ml) and H2O (15 ml). The reaction mixture was filtered to remove the granular precipitate and washed thoroughly with ether. The filtrate was washed successively with 1N HCl, NaHCO3 (saturated aqueous), and brine. The combined organic layers were dried over MgSO4 and concentrated in vacuo to give (E)-2-methyl-but-2-en-1-ol (2) as a clear oil (12.8 g, 74%).

[0405] Method C: Representative Procedure for Alkylation of Phenols Alcohols.

[0406] 3-Hydroxybenzylalcohol (1) (0.500 g 4.03 mmol) was dissolved in DMF (2 mL) at ambient temperature. Ethyl bromide (0.900 mL, 12.1 mmol) and finely crushed K2CO3 (2.78 g, 20.1 mmol) were added and the reaction mixture was stirred for 5 h. The DMF was then removed in vacuo and the residue was partitioned between EtOAc and H2O, and extracted with EtOAc (3×10 mL). The organic layers were washed with brine (10 mL) and passed over a short plug of Na2SO4. The solvents were removed in vacuo to give alcohol 2 (0.55 g, 90%) as a pale yellow, thick oil, which was of sufficient quality to be advanced to the next step without further purification. Rf (40% EtOAC/hexanes): 0.69.

[0407] Method D: Representative Procedure for Conversion of Alcohols to Amines.

[0408] 3-Ethoxy-phenyl-methanol (1) (1.23 g 8.08 mmol) was dissolved in CH2Cl2 (10 mL) at ambient temperature and diphenylphosphoryl azide (2.67 g, 9.70 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (1.45 mL, 9.70 mmol) were added. The mixture was stirred for 5 h at which time the CH2Cl2 was removed in vacuo and the crude residue was partitioned between EtOAc and H2O and extracted with EtOAc (3×10 mL). The combined organic layers were washed with brine (10 mL), passed over a short plug of Na2SO4, and concentrated in vacuo to give a yellow oil that was loaded directly onto a flash silica gel column and was quickly eluted with 10% EtOAc/hexanes. The solvents were removed in vacuo to give azide 2 (1.43 g, 84%) as a colorless oil. Rf (30% EtOAc/hexanes): 0.79.

[0409] 1-Azidomethyl-3-ethoxy-benzene (2) (1.19 g 6.71 mmol) was dissolved in MeOH (15 mL) and palladium 10% on activated carbon, wet (20% in weight) was added. The reaction was hydrogenated for 30 min at 40 PSI in a Parr Hydrogenator. The black suspension was then filtered through compacted celite and the methanol was removed in vacuo to give amine 3 (0.88 g, 88%) as a pale yellow, thick oil, which was of sufficient quality to be advanced to the coupling reactions without further purification.

[0410] Method E: Representative Procedure for Conversion of Alcohols to Bromides.

[0411] Cis-2-penten-1-ol (1) (1.00 g, 11.6 mmol) and carbon tetrabromide (3.85 g, 13.9 mmol) were dissolved in CH2Cl2 (75 mL). The mixture was cooled to 0° C. and triphenylphosphine (3.65 mL, 13.9 mmol) dissolved in CH2Cl2 (50 mL) was added dropwise. The mixture was allowed to warm to room temperature and was stirred overnight. The CH2Cl2 was removed in vacuo and the crude residue was loaded directly onto a flash silica gel column and eluted quickly with 20% EtOAc/hexanes. The solvents were removed in vacuo to give bromide 2 (1.53 g, 88%) as a colorless volatile oil. Rf (30% EtOAC/hexanes): 0.89.

[0412] Method F: Representative Procedure for Conversion of Bromides to Amines.

[0413] A mixture of bromide 1 (3.00 g, 20.1 mmol), di-tert-butyl-iminodicarboxylate (4.8 g, 22 mmol), and K2CO3 (3.10 g, 80.4 mmol) in DMF (30 ml) was stirred at ambient temperature overnight. The mixture was partitioned between 1N HCl and EtOAc. The organic layer was washed with H2O and brine, then dried over NaSO4. Concentration in vacuo affored a yellow oil which upon purification by flash column chromatography (hexanes to 5% EtOAc/Hexane gradient) yielded protected amine 2 as a clear oil (2.0 g, 35%).

[0414] A mixture of the diBOC amine 2 (2.0 g, 7.0 mmol), trifluoroacetic acid (2.7 ml, 35 mmol) and CH2Cl2 (40 ml) was stirred at ambient temperature overnight. The reaction mixture was concentrated in vacuo to give the TFA salt of (E)-2-methyl-but-2-enylamine (3).

[0415] Method G: Representative Procedure for Reduction of Aromatic Nitro Groups by Hydrogenation.

[0416] Compound 1 (2.04, 5.79 mmol) was dissolved in EtOAc (20 mL) and palladium 10% on activated carbon, wet (20% in weight) was added. The reaction was hydrogenated for 4 h at 45 PSI in a Parr Hydrogenator. The black suspension was then filtered through compacted celite and the methanol was removed in vacuo to give aniline 2 (1.65 g, 88%) as a pale yellow, thick oil, which was of sufficient quality to be advanced to the acetylation reaction without further purification.

[0417] Method H: Representative Procedure for Acetylation of Anilines.

[0418] Aniline 1 (1.65 g, 5.12 mmol) was dissolved in CH2Cl2 (25 mL) at ambient temperature. Acetyl chloride (0.48 g, 6.14 mmol) and N,N-Diisopropylethylamine (0.79 g, 6.14 mmol) were added, and the reaction was stirred overnight. The CH2Cl2 was removed in vacuo and the crude residue was partitioned between EtOAc and 5% KHSO4 and extracted with EtOAc (3×10 mL). The combined organic extracts were washed with NaHCO3 (saturated aqueous, 10 mL), brine (10 mL), and dried over Na2SO4. The solvents were removed in vacuo to give an orange oil which was of sufficient quality to be advanced to the next step without further purification. Rf (50% EtOAC/hexanes): 0.42.

[0419] Method I: Representative Procedure for Reduction of Aldehydes to Amines.

[0420] Hydroxyl amine hydrochloride (758 mg, 10.7 mmol) and pyridine (2.16 mL) was added to a solution of 2,2-difluoro-5-formyl benzodioxole (1) (2.00 g, 10.7 mmol) in MeOH (10 mL). After 18 hours the MeOH was removed in vacuo. The reaction mixture was diluted with EtOAc and was washed sequentially with H2O, 10% w/v CuSO4, and brine and then dried over MgSO4. The solution was concentrated in vacuo. The hydroxy imine was purified by column chromatography using 20% EtOAc/Hexanes to give 1.37 g (64% yield) of a white solid. Imine was then subjected to LAH reduction as described above to provide amine 3.

[0421] Method J: Representative Procedure for the Hydroxylation of a Substituted Benzoic Acid

[0422] 2,5-dimethyl-benzoic acid (1) (20 g, 133 mmol) was dissolved in concentrated H2SO4 (30 mL) and fuming H2SO4 (20% SO3, 70 mL). The reaction mixture was heated to 110° C. for 2 hours. After cooling, the solution was poured carefully into a beaker of ice H2O (400 mL) and was then neutralized with 20% aqueous NaOH (400 mL). The H2O was partially removed in vacuo until a white salt mixture started to form. The solid was collected on a sintered-glass funnel and was then dried in a vacuum oven. The dried salt mixture was placed in a ceramic crucible with KOH (160 g) and was melted together using a butane torch for 0.5 h. After cooling, the fused solid was dissolved in H2O (300 mL) and acidified with concentrated HCl (300 mL). The product was extracted from the aqueous solution with EtOAc (3×200 mL). The combined organic layers were washed with brine (100 mL) and dried over MgSO4. The solvents were removed in vacuo and the solid residue was recrystallized with 20% EtOAc/CHCl3 four times to afford 3-hydroxy-2,5-dimethyl-benzoic acid (2) as a light brown solid (9.8 g, 44%)

[0423]

1
H NMR (Acetone-d6) δ 10.93 (br s, 1H), 8.34 (br s, 1H), 7.20 (s, 1H), 6.86 (s, 1H), 2.37 (s, 3H), 2.24 (s, 3H).

REFERENCES

[0424] Fujiwara, A. N.; Acton, E. M. Can. J. Chem. 1970, 48, 1346-1349.

[0425] Charlesworth, E. H.; Levene, L. Can. J. Chem. 1963, 41, 1071-1077.

[0426] The following amines were synthesized for the corresponding example numbers:

EXAMPLE A35 AND EXAMPLE A36

[0427]

[0428] Amines were generated from reducing the corresponding ketone as described in method A above followed by conversion to the azide and reduction as described in method D above. The mixture of isomers was coupled to the chiral thiazolidine core and separated.

EXAMPLE A37 AND EXAMPLE A38

[0429]

[0430] Amines were generated as described for Examples A35 and A36, separating the diastereomers at the thiazolidine stage.

EXAMPLE A84 AND EXAMPLE A85

[0431]

[0432] Amines were generated as described for Examples A35 and A36, separating the diastereomers at the thiazolidine stage.

EXAMPLE A86 AND EXAMPLE A87

[0433]

[0434] Amines were generated as described for Example A35 and A36, separating the diastereomers at the thiazolidine stage.

EXAMPLE A43

[0435]

100

[0436] Amine was generated by alkylation of 3-hydroxybenzyl alcohol with ethyl bromide as describe in method C above followed by conversion of the alcohol to the amine as described in method D above provided desired amine.

EXAMPLE A44

[0437]

101

[0438] Amine was generated as described above for Example A43 using the cyclopropyl alkylating agent.

EXAMPLE A93

[0439]

102

[0440] Amine was generated as described above for Example A43 using propylbromide as the alkylating agent.

EXAMPLE A67

[0441]

103

[0442] Amine was generated from displacement of bromide in 3-nitrobenzylbromide with di BOC amine as described in method F above. Reduction of the nitro moiety to the aniline (method G above) followed by acetylation (method H above) and BOC removal (method F above) provided desired amine.

EXAMPLE A72, EXAMPLE A73 AND EXAMPLE A80

[0443]

104

[0444] Amines were generated from conversion of the corresponding primary alcohols as described in method E above. Displacement of the bromide with di BOC amine and deprotection with TFA (method F above) provided the desired amines.

EXAMPLE A77

[0445]

105

[0446] Amine was generated from 3-dimethylaminobenzyl alcohol as described in method D above.

EXAMPLE A48

[0447]

106

[0448] Amine was generated by bromination of the corresponding methyl compound (Nussbaumer, P., et. al. J. Med Chem., 1991, 34, 65-73.). Conversion of the bromide to the amine was accomplished by azide displacement of the bromide followed by reduction as described in method D above.

EXAMPLE A69

[0449]

107

[0450] Amine was generated by reduction of the corresponding methyl ester to the primary alcohol (Wipf, J. Org. Chem. 1994, 59, 4875-86.). Conversion to the bromide (method E above) followed by displacement with diBOC amine and deprotection (method F above) provided desired amine.

EXAMPLE A70 AND EXAMPLE A71

[0451]

108

[0452] Amines were generated from the corresponding carboxylic acids. Reduction of the acid as described in method B above followed by bromide displacement as described in method E above gave the primary bromide. Conversion of the bromide to the primary amine followed the procedure described in method F above.

EXAMPLE A74

[0453]

109

[0454] Amine was generated from the primary alcohol as described in method D above.

EXAMPLE A76

[0455]

110

[0456] Amine was generated by first reduction of the corresponding aldehyde with sodium borohydride to the primary alcohol (Dondoni, J. Org. Chem. 1995, 60, 4749-54.). The alcohol was then converted to the amine as described in method D above.

EXAMPLE A82 AND EXAMPLE A83

[0457]

111

[0458] Amines were generated by conversion of the primary alcohol as described in method D above. Tetrahydrofuran amine (Example A83) was the byproduct of over-reduction of A82.

EXAMPLE A91

[0459]

112

[0460] Amine was generated from the corresponding carboxylic acid. Reduction of the acid as described in method B above gave the primary alcohol. The alcohol was then converted to the amine using the procedure described in method D above.

EXAMPLE A92

[0461]

113

[0462] Amine was generated from 3-benzyloxybenzyl alcohol. Conversion to the azide and reduction of both the azide and benzyl protecting group were accomplished using method D as described above with longer hydrogenation time.

EXAMPLE A94

[0463]

114

[0464] Amine was generated by LiAlH4 reduction of 2-cyanophenol (Ludeman, S. M., et. al. J. Med. Chem. 1975, 18, 1252-3.).

EXAMPLE A88 AND EXAMPLE A89

[0465]

115

[0466] Amines were generated from the corresponding achiral ketone prepared by the method of Haunz (Huanz, et. al. Synth. Commun. 1998, 28, 1197-1200.). The ketone was reduced to the alcohol as a mixture of isomers using method A as described above. The mixture was converted to a mixture of amines by the procedure described in method D above. The amines were coupled to the thiazolidine core as a mixture and were then separated to provide Examples A88 and A89.

EXAMPLE A78 AND EXAMPLE A79

[0467]

116

[0468] Amines were generated from the corresponding achiral ketone prepared by the method of Bell (Bell, et. al. J. Med. Chem. 1998, 41, 2146-63.). The ketone was reduced to the alcohol as a mixture of isomers using method A as described above. The mixture was converted to a mixture of amines by the procedure described in method D above. The amines were coupled to the thiazolidine core as a mixture and were then separated to provide Examples A78 and A 79.

EXAMPLE A81

[0469]

117

[0470] Amine was generated from the corresponding carboxylic acid. Reduction of the acid using the procedure described in method A above provided the primary alcohol which was converted to the bromide using the method of Onda (Onda, M. et. al. Chem. Pharm. Bull. 1971, 10, 2013-19.). The bromide was then converted to the amine using the procedure described in method F above.

EXAMPLE A110

[0471]

118

[0472] Amine was generated from the condensation of o-tolualdehyde with 2-aminoethanol followed by reduction with sodium borohydride (Tetrahedron Assym. 1997, 8, 2367-74.).

EXAMPLE A103

[0473]

119

[0474] Amine was generated from the corresponding aldehyde by the reductive amination procedure described in method I above.

EXAMPLE A105

[0475]

120

[0476] Amine was generated by reduction of the corresponding methyl ester to the primary alcohol (Wipf, J. Org. Chem. 1994, 59, 4875-86.). The alcohol was converted to the amine by the procedure described in method D above.

EXAMPLE A107

[0477]

121

[0478] Amine was generated from reduction of the corresponding carboxylic acid to the primary alcohol as described in method A above. The alcohol was converted to the amine using the procedure described in method D above.

EXAMPLE A106 AND EXAMPLE A97

[0479]

122

[0480] Amines were generated by the borane reduction of the corresponding carboxylic acids to the primary alcohols. The alcohols were converted to the amines using the procedure described in method D above.

EXAMPLE A46

[0481]

123

[0482] Amine was generated by the condensation of ethylacetoacetate with cyanoacetamide followed by reaction with phosphorus oxychloride to provide 3-cyano-2,5-dihydroxy-4-methylpyridine. Hydrogenation with palladium dichloride gave the 3-cyano-4-methylpyridine which was hydrogenated with Raney nickel in ammonia and ethanol to afford the desired amine (J. Org. Chem. 1959, 25, 560.).

EXAMPLE A10

[0483]

124

[0484] Amine was generated by a reductive amination with the corresponding aldehyde (Arch. Pharm. 1987, 320, 647-54.).

EXAMPLE A109

[0485]

125

[0486] Amine was generated on the thiazolidine core as follows:

126

[0487] Diphenylchlorophosphate (1.0 ml, 4.2 mmol) followed by triethylamine (0.59 ml, 4.2 mmol) were added to a cooled 0° C. solution of BOC-DMTA 1 (1.0 g, 3.8 mmol) in EtOAc (10 ml). The mixture was stirred for 1 h and at which time triethylamine (0.59 ml, 4.2 mmol) and ethanolamine (0.25 ml, 4.2 mmol) were added. The reaction was left to stir overnight at ambient temperature and then partitioned between 1N HCl and EtOAc. The organic layer was washed with NaHCO3(saturated aqueous) and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to a pale yellow oil 2. The oil was stirred with thionyl chloride (2 ml) for 45 min at room temperature. The mixture was concentrated in vacuo and the residual oil was partitioned between 1N NaOH and EtOAc. The organic layer was extracted with 1N HCl (2×20 ml). The combined aqueous layers were made basic with 1N NaOH and then extracted with EtOAc (3×60 ml). The organic layers were washed with brine, dried over Na2SO4 and concentrated in vacuo to give (R)-5,5-Dimethyl-thiazolidine-4-carboxylic acid (2-chloro-ethyl)-amide 3 as a clear oil (0.39 g, 55%).

[0488] The following amines were prepared as described:

127

[0489] The above amines were prepared according to Carlsen, H. J., J. Heterocycle Chem. 1997, 34, 797-806.

128

[0490] The above amine was prepared according to O'Brien, P. M., J. Med. Chem. 1994, 37, 1810-1822.

129

[0491] The above amine was prepared according to Weinheim, G. Arch. Pharm. 1987, 320, 647-654.

[0492] General Method A

130

[0493] The synthesis of compounds with the general structure 5 is as follows. The boc-protected thiazolidine carboxylic acid 1 is coupled to the requisite amines 2 to yield amino amides 3 using a two step process. The process includes treatment of 1 with 2 in the presence of either diphenylchlophosphate or HATU, followed by exposure to methane sulfonic acid. Final compounds 5 are obtained by a DCC-mediated coupling of 3 and 4 followed by deprotection of the P2 phenol. Final compounds were purified either by flash chromatography or preparative HPLC.

131

[0494] An alternative approach to the general structure 5 is as follows. The thiazolidine ester 6 is coupled to acid 7 under carbodiimide reaction conditions, resulting in product 8 which is converted to acid 9 by mild base hydrolysis. Acid 9 is combined with various amines, using diphenylphosphoryl azide, followed by cleavage of the P2 acetate to yield final compounds 5. The products were purified by either flash chromatography or preparative HPLC.

[0495] Specific Method A.

EXAMPLE A1

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (1,2,3,4-tetrahydro-naphthalen-1-yl)-amide

[0496]

132

[0497] The title compound was prepared as follows. (R)-5,5-Dimethyl-thiazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 1 (0.3 g, 1.15 mmol) was dissolved in EtOAc (3 mL) and cooled to 0° C. Diphenyl chlorophosphate (0.26 mL, 1.26 mmol) was added followed by TEA (0.18 mL, 1.26 mmol). The reaction was stirred at 0° C. for 1 h, and treated with (S)-1,2,3,4-Tetrahydro-1-naphthylamine (0.19 g, 1.26 mmol). The reaction mixture was stirred at room temperature overnight, then partitioned between 1N HCl (5 mL) and EtOAc (10 mL). The organic layer was washed with saturated NaHCO3, brine, dried over Na2SO4 and concentrated to a light yellow oil. The resulting crude oil was dissolved in EtOAc (5 mL) and the cooled to 0° C. Methanesulfonic acid (0.36 mL, 5.32 mmol) was added and the solution was stirred at 0° C. for 15 minutes, then at room temperature for 1 h. The mixture was re-cooled to 0° C. and quenched with 5% Na2CO3 (5 mL) then extracted with EtOAc (10 mL). The organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo to give 3 as a yellow oil. The yellow oil 3 (0.34 g, 1.15 mmol) was dissolved in EtOAc (12 mL). AMB-AHPBA 4 (0.40 g, 1.09 mmol) was added followed by HOBt (0.15 g, 1.09 mmol). The mixture was stirred at room temperature 1 h, then cooled to 0° C. DCC (0.24 g, 1.15 mmol) was slowly added as solution in EtOAc (6 mL). The mixture was warmed to room temperature and stirred overnight. The mixture was filtered and the filtrate was washed with 1N HCl (10 mL), saturated NaHCO3 (10 mL), brine (10 mL), dried over Na2SO4 and concentrated to give a crude white solid (contaminated with DCU). The DCU was removed by flash chromatography (30% to 50% EtOAc in hexanes) to provide a white solid, which was dissolved in MeOH (2 mL) and treated with 4N HCl in 1,4-dioxane (0.26 mL, 1.1 mmol). The reaction was stirred at room temperature overnight then partitioned between 1N HCl (10 mL) and EtOAc (10 mL). The organic layer was washed with saturated NaHCO3, dried over Na2SO4 and concentrated to a residue which was purified by flash chromatography (60% EtOAc in hexanes) to provide the title compound as a white solid: mp=125-126° C.; IR (cm−1) 3320, 2932, 1704, 1644, 1530, 1454, 1361, 1284; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.28 (d, J=8.6, 1H), 8.21 (d, J=8.8, 1H), 7.35-6.91 (m, 10H), 6.76 (d, J=8.0, 1H), 6.54 (d, J=7.5, 1H), 5.34 (d, J=6.0, 1H), 5.13 (d, J=9.0, 1H), 5.02 (d, J=9.0, 1H), 4.60-4.30 (m, 4H), 2.81-2.68 (m, 4H), 1.81 (s, 3H), 1.78-1.60 (m, 4H), 1.48 (s, 3H), 1.45 (s, 3H); Anal. Calcd for C34H39N3O5S.1.5H2O: C, 64.95; H, 6.73; N, 6.68. Found: C, 64.88; H, 6.31; N, 6.18.

EXAMPLE A2

(R)-3-((2S,3R)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid 3-methoxy-benzylamide

[0498]

133

[0499] White solid: mp 108-110° C.; IR (neat, cm−1) 3310, 2965, 1644, 1586, 1531, 1455, 1359, 1284; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.40 (t, J=6.0, 1H), 8.09 (d, J=8.1, 1H), 7.31-6.52 (m, 12H), 5.49 (d, J=6.0, 1H), 5.12 (d, J=9.3, 1H), 5.00 (d, J=9.3, 1H), 4.44-4.35 (m, 3H), 4.42 (s, 1H), 4.09 (dd, J=15.0, 6.0, 1H), 3.69 (s, 3H), 2.87-2.67 (m, 2H), 1.82 (s, 3H), 1.49 (s, 3H), 1.34 (s, 3H); Anal. Calcd for C32H37N3O6S.0.75H2O: C, 63.50; H, 6.41; N, 6.94. Found: C, 63.60; H, 6.23; N, 6.80.

[0500] The following examples were prepared by the specific method outlined above using the requisite amine 2.

EXAMPLE A3

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (pyridin-2-ylmethyl)-amide

[0501]

134

[0502] IR (neat cm−1) 3315, 1642, 1529, 1437, 1372, 1284; 1H NMR (DMSO-d6) δ 9.38 (s, 1H), 8.59 (t, J=5.0, 1H), 8.45 (d, J=4.0, 1H), 8.15 (d, J=8.2, 1H), 7.65 (td, J=7.5, 1.8, 1H), 7.39 (d, J=7.9, 1H), 7.29-7.11 (m, 7H), 6.93 (t, J=7.7, 1H), 6.77 (d, J=8.1, 1H), 6.54 (d, J=7.0, 1H), 5.51 (d, J=6.6, 1H), 5.15 (d, J=9.2, 1H), 5.03 (d, J=9.2, 1H), 4.50-4.26 (m, 5H), 2.87-2.68 (m, 2H), 1.82 (s, 3H), 1.52 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C30H34N4O5SNa (M+Na)+ 585.2148, found 585.2141.

EXAMPLE A4

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (1,2,3,4-tetrahydro-naphthalen-1-yl)-amide

[0503]

135

[0504] White solid: mp=123-125° C.; IR (cm−1) 3314, 2932, 1704, 1644, 1584, 1530, 1454, 1360, 1284; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.42 (d, J=8.6, 1H), 8.23 (d, J=8.0, 1H), 7.38-6.90 (m, 10H), 6.77 (d, J=8.0, 1H), 6.45 (d, J=6.0, 1H), 5.45 (d, J=6.0, 1H,), 5.02 (d, J=9.0, 1H), 4.99 (d, J=9.0, 1H), 5.11-4.40 (m, 4H), 2.90-2.69 (m, 4H), 1.81 (s, 3H), 1.77-1.58 (m, 4H), 1.49 (s, 3H), 1.42 (s, 3H); Anal. Calcd for C34H39N3O5S.1.25H2O: C, 65.42; H, 6.70; N, 6.73. Found: C, 65.41; H, 6.46; N, 6.60.

EXAMPLE A5

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (pyridin-3-ylmethyl)-amide

[0505]

136

[0506] IR (neat cm−1) 3310, 2931, 1642, 1537, 1455, 1373, 1279; 1H NMR (DMSO-d6) δ 9.39 (s, 1H), 8.55-8.50 (m, 2H), 8.38 (s, 1H), 8.15 (d, J=8.2, 1H), 7.68 (d, J=8.1, 1H), 7.30-7.14 (m, 6H), 6.94 (t, J=7.5, 1H), 6.77 (d, J=8.1, 1H), 6.54 (d, J=7.7, 1H), 5.51 (d, J=6.6, 1H), 5.14 (d, J=9.2, 1H), 5.03 (d, J=9.2, 1H), 4.49-4.41 (m, 4H), 4.18 (dd, J=15.4, 5.5, 1H), 2.85-2.67 (m, 2H), 1.81 (s, 3H), 1.49 (s, 3H), 1.31 (s, 3H); HRMS (ESI) m/z calcd for C30H35N4O5S (M+H)+ 563.2323, found 563.233)7.

EXAMPLE A6

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiiazolidine-4-carboxylic Acid methyl-(3-methyl-thiophen-2-ylmethyl)-amide

[0507]

137

[0508] IR (neat or KBr cm−1) 3150, 3000, 2942, 2187, 1712, 1600, 1567, 1505; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.44 (t, J=7.98, 1H), 8.13-8.07 (m, 2H), 7.34-7.13 (m, 5H), 6.93 (t, J=7.9, 1H), 6.78 (d, J=7.7, 1H), 6.53 (d, J=7.1, 1H), 5.45 (d, J=7.0, 1H), 5.12 (dd, J=7.8, 8.2 1H), 4.51-4.31(m, 4H), 2.86-2.67 (m, 2H), 2.19 (s, 3H), 1.81 (s, 3H), 1.51 (s, 3H), 1.34 (s, 3H); Anal. Calcd for C30H35N3O5S2: calculated C, 61.94; H, 6.06; N, 7.22. Found C, 62.38; H, 6.23; N, 7.17.

EXAMPLE A7

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (benzo[b]thiophen-3-ylmethyl)-amide

[0509]

138

[0510] IR (neat cm−1) 3401, 2931, 1637, 1531, 1455, 1367, 1284, 1108; 1H NMR (DMSO-d6) δ 9.39 (s, 1H), 8.52 (t, J=5.7, 1H), 8.17 (d, J=8.2, 1H), 7.93 (d, J=6.4, 1H), 7.86 (d, J=6.9, 1H), 7.57 (s, 1H), 7.35-7.11 (m, 7H), 6.94 (t, J=7.9, 1H), 6.78 (d, J=7.9, 1H), 6.56 (d, J=7.5, 1H), 5.47 (d, J=5.0, 1H), 5.16 (d, J=9.2, 1H), 5.02 (d, J=9.2, 1H), 4.67 (dd, J=15.2, 5.9, 1H), 4.47-4.34 (m, 4H), 2.89-2.70 (m, 2H), 1.83 (s, 3H), 1.49 (s, 3H), 1.34 (s, 3H); HRMS (ESI) m/z calcd for C33H35N3O5S2Na (M+Na)+ 640.1910, found 640.1919; Anal. Calcd for C33H35N3O5S2.H2O: C, 62.34; H, 5.87; N, 6.61. Found: C, 62.93; H, 5.80; N, 6.57.

EXAMPLE A8

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (pyridin-4-ylmethyl)-amide

[0511]

139

[0512]

1
H NMR (DMSO-d6) δ 9.38 (s, 1H), 8.55 (t, J=6.2, 1H), 8.42 (m, 1H), 8.13 (d, J=8.2, 1H), 7.30-7.19 (m, 7H), 6.94 (t, J=7.7, 1H), 6.77 (d, J=7.7, 1H), 6.54 (d, J=7.1, 1H), 5.54 (d, J=6.8, 1H), 5.15 (d, J=9.1, 1H), 5.02 (d, J=9.1, 1H), 4.48-4.13 (m, 5H), 2.87-2.68 (m, 2H), 1.81 (s, 3H), 1.52 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C30H34N4O5SNa (M+Na)+ 585.2142, found 585.2153.

EXAMPLE A9

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (2,3-dihydro-benzofuran-5-ylmethyl)-amide

[0513]

140

[0514] IR (neat, cm−1) 3330, 2919, 1643, 1490, 1443, 11367, 1284, 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.35 (m, 1H), 8.12 (d, J=7.9, 1H), 7.32-7.09 (m, 6H), 6.99-6.91 (m, 2H), 6.77 (d, J=8.1, 1H), 6.68-6.53 (m, 2H), 5.45 (d, J=6.2, 1H), 5.12 (d, J=8.8, 1H), 5.00 (d, J=8.9, 1H), 4.50-4.39 (m, 6H), 4.29 (dd, J=14.5, 6.2, 1H), 4.14-4.04 (m, 2H), 3.15-2.99 (m, 2H), 1.81 (s, 3H), 1.48 (s, 3H), 1.33 (s, 3H); HRMS (ESI) m/z calcd for C33H37N3O6SNa (M+Na)+ 626.2295, found 626.2283.

EXAMPLE A10

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (3-methyl-pyridin-4-ylmethyl)-amide

[0515]

141

[0516]

1
H NMR (DMSO-d6) δ 9.34 (s, 1H), 8.47 (t, J=6.0, 1H), 8.29 (m, 2H), 8.11 (d, J=8.3, 1H), 7.32-7.14 (m, 6H), 6.94 (t, J=7.7, 1H), 6.78 (dd, J=7.7, 1.0, 1H), 6.55 (dd, J=7.7, 1.0, 1H), 5.49 (d, J=6.7, 1H), 5.16 (d, J=9.1, 1H), 5.03 (d, J=9.1, 1H), 4.51-4.38 (m, 3H), 4.49 (s, 1H), 4.13 (dd, J=16.4, 5.1, 1H), 2.88-2.69 (m, 2H), 2.25 (s, 3H), 1.83 (s, 3H), 1.53 (s, 3H), 1.37 (s, 3H); HRMS (ESI) m/z calcd for C31H37N4O5S (M+H)+ 577.2485, found 577.2463; Anal. Calcd for C31H36N4O5S.0.3H2O: C, 63.96; H, 6.34; N, 9.63; S, 5.51. Found: C, 63.95; H, 6.42; N, 9.51; S, 5.22.

EXAMPLE A11

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (naphthalen-1-ylmethyl)-amide

[0517]

142

[0518] IR (neat, cm−) 3425, 1643, 1531, 1455, 1378, 1290, 1108, 1H NMR (DMSO-d6) δ 9.39 (s, 1H), 8.50 (t, J=5.9, 1H), 8.15 (d, J=8.0, 2H), 8.07 (d, J=9.0, 1H), 7.90 (d, J=7.1, 1H), 7.81 (d, J=8.1, 1H), 7.54-7.12 (m, 9H), 6.95 (d, J=7.0, 1H), 6.78 (d, J=8.1, 1H), 6.56 (d, J=7.0, 1H), 5.15 (d, J=9.2, 1H), 5.01 (d, J=9.2, 1H), 4.95-4.86 (m, 1H), 4.76-4.48 (m, 4H), 2.90-2.71 (m, 2H), 1.84 (s, 3H), 1.47 (s, 3H), 1.34 (s, 3H); HRMS (ESI) m/z calcd for C35H37N3O5SNa (M+Na)+ 634.2346, found 634.2332.

EXAMPLE A12

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid [(R)-1-(tetrahydro-furan-2-yl)methyl]-amide

[0519]

143

[0520] White solid: mp=105-107° C.; IR (cm−1) 3339, 1644, 1537, 1454, 1372, 1285, 1079; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.12 (d, J=8.8, 1H), 8.01 (t, J=5.0, 1H), 7.34-7.15 (m, 5H), 6.93 (t, J=7.5, 1H), 6.76 (d, J=7.5, 1H), 6.53 (d, J=7.5, 1H), 5.45 (d, J=5.5, 1H), 5.07 (d, J=9.3, 1H), 4.99 (d, J=9.3, 1H), 4.50-4.10 (m, 3H), 3.83-3.55 (m, 5H), 3.20-3.00 (m, 2H); 2.90-2.60 (m, 2H), 1.90-1.70 (m, 2H), 1.79 (s, 3H), 1.48 (s, 3H), 1.34 (s, 3H); Anal. Calcd for C29H37N3O6S.0.5H2O: C, 61.68; H, 6.78; N, 7.44. Found: C, 61.46; H, 6.74; N, 7.47.

EXAMPLE A13

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiiazolidine-4-carboxylic Acid cyclohexylmethyl-amide

[0521]

144

[0522] IR (neat or KBr cm−1) 3743, 2924, 2360, 1868, 1844, 1771, 1699, 1646; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.13 (d, J=7.9 1H), 7.85 (t, J=7.2, 1H), 7.34-7.13 (m, 5H), 6.93 (t, J=7.9, 1H), 6.78 (d, J=7.7, 1H), 6.53 (d, J=7.1, 1H), 5.15 (d, J=7.0, 1H), 5.08 (d, J=7.8, 1H), 4.81 (s, 1H), 4.51 (d, J=6.2 1H), 4.46(s, 1H), 4.38 (d, J=6.32, 1H), 4.31(s, 6H) 2.86-2.67 (m, 4H), 2.55 (s, 1H), 1.81 (s, 3H), 1.64-1.54 (m, 6H), 1.51 (s, 3H), 1.39 (s, 3H), 1.18-1.08 (m, 4H), 0.99-0.78 (m, 3H); Anal. Calcd for C32H47N3O6S.0.3 TFA.0.75H2O: C, 61.67; H, 7.01; N, 6.83. Found: C, 61.78; H, 6.66; N, 6.63.

EXAMPLE A14

3-((2S,3S)-2-Hydroxy-3-{1[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (benzo[1,3]dioxol-5-ylmethyl)-amide

[0523]

145

[0524] IR (neat or KBr cm−1) 3302, 2922, 2351, 2333, 1768, 1750, 1646, 1537; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.44 (s, 1H), 8.13 (d, J=7.9 1H), 7.34-7.13 (m, 5H), 6.99-6.77 (m, 4H), 6.78 (d, J=7.7, 1H), 5.93 (d, J=7.1, 2H), 5.15 (d, J=7.0, 1H), 5.08 (d, J=7.8, 1H), 4.43 (d, J=9.32, 2H), 4.34 (m, 2H), 4.12(d, J=6.18, 1H), 4.08 (d, J=6.08, 1H), 2.86-2.67 (m, 2H), 2.55 (s, 1H), 1.81 (s, 3H), 1.51 (s, 3H), 1.39 (s, 3H); Anal. Calcd C32H35N3O7S.0.65 TFA.1.0H2O: C, 57.31; H, 5.44; N, 6.02. Found: C, 57.58; H, 5.47; N, 5.85.

EXAMPLE A15

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (furan-2-ylmethyl)-amide

[0525]

146

[0526] IR (neat or KBr cm−) 3311, 2931, 2360, 2333, 1732, 1718, 1695, 1646; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.44 (t, J=6.98, 1H), 8.13 (d, J=7.9 1H), 7.53 (s, 1H), 7.34-7.13 (m, 5H), 6.95 (t, J=7.8, 1H), 6.78 (d, J=7.7, 1H), 6.56 (d, J=7.4, 1H), 6.35 (d, J=7.1, 1H), 6.26 (d, J=7.12, 1H), 5.15 (d, J=7.0, 1H), 5.08 (d, J=7.8, 1H), 4.45 (d, J=7.5, 1H), 4.34-4.22 (m, 4H), 4.20 (m, 2H), 2.86-2.67 (m, 2H), 1.81 (s, 3H), 1.51 (s, 3H), 1.39 (s, 3H); Anal. Calcd C29H33N3O6S.0.2 TFA.1.0H2O: C, 59.60; H, 5.99; N, 7.09. Found C, 59.68; H, 5.73; N, 6.97.

EXAMPLE A16

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (R)-chroman-4-ylamide

[0527]

147

[0528] White solid: mp=135-136° C.; IR (cm−1) 3312, 2928, 1644, 1584, 1520, 1489, 1454, 1283, 1105; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.55 (d, J=8.2, 1H), 8.20 (d, J=8.9, 1H), 7.36 (d, J=7.2, 2H,) 7.26-7.07 (m, 5H); 6.95-6.90 (m, 1H), 6.81-6.73 (m, 3H), 6.54 (d, J=7.2, 1H), 5.47 (d, J=6.9, 1H), 5.16 (d, J=8.9, 1H), 5.01 (d, J=8.9, 1H), 4.54-4.32 (m, 4H), 4.22-4.12 (m, 2H), 2.94-2.64 (m, 2H), 2.10-1.90 (m, 2H), 1.80 (s, 3H), 1.49 (s, 3H), 1.41 (s, 3H); Anal. Calcd for C33H37N3O6S.1.25H2O: C, 63.29; H, 6.36; N, 6.71. Found: C, 63.22; H, 6.18; N, 6.51.

EXAMPLE A17

(R)-3-((2S,3S)-2-Hydroxy-3-{1[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-chroman-4-ylamide

[0529]

148

[0530] White solid: mp=135-136° C.; IR (cm−1) 3311, 2928, 1644, 1584, 1520, 1489, 1454, 1283, 1105; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.49 (d, J=8.2, 1H), 8.23 (d, J=8.4, 1H); 7.33-7.10 (m, 7H), 6.94-6.75 (m, 4H), 6.54 (d, J=7.7, 1H), 5.34 (d, J=7.2, 1H), 5.14 (d, J=8.9, 1H), 5.01 (d, J=8.9, 1H), 4.54-4.30 (m, 4H), 4.24-4.10 (m, 2H), 2.82-2.62 (m, 2H),2.10-1.90 (m, 2H), 1.79 (s, 3H), 1.49 (s, 3H), 1.45 (s, 3H); Anal. Calcd for C33H37N3O6S.0.25H2O: C, 65.17; H, 6.21; N, 6.91. Found: C, 65.24; H, 6.28; N, 6.95.

EXAMPLE A18

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (R)-thiochroman-4-ylamide

[0531]

149

[0532] White solid: mp=125-127° C.; IR (cm−1) 3313, 2926, 1644, 1585, 1520, 1455, 1285, 1081, 1048; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.61 (d, J=8.3, 1H), 8.20 (d, J=8.6, 1H), 7.38-6.90 (m, 10H), 6.76 (d, J=8.1, 1H), 6.54 (d, J=7.9, 1H), 5.46 (d, J=6.6, 1H), 5.17 (d, J=9.0, 1H), 5.01 (d, J=9.0, 1H), 4.56-4.21 (m, 4H), 3.20-2.61 (m, 4H), 2.30-2.00 (m, 2H), 1.79 (s, 3H), 1.49 (s, 3H), 1.41 (s, 3H); Anal. Calcd for C33H37N3O5S2.0.5H2O: C, 63.03; H, 6.09; N, 6.68. Found: C, 62.84; H, 6.29; N, 6.38.

EXAMPLE A19

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-thiochroman-4-ylamide

[0533]

150

[0534] White solid: mp=125-127° C.; IR (cm−1) 3312, 2927, 1644, 1585, 1520, 1455, 1372, 1285; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.47 (d, J=7.5, 1H), 8.23 (d, J=7.7, 1H), 7.37-6.91 (m, 10H), 6.76 (d, J=8.6, 1H), 6.54 (d, J=7.5, 1H), 5.33 (d, J=6.8, 1H), 5.15 (d, J=9.0, 1H), 5.00 (d, J=9.0, 1H), 4.60-4.30 (m, 4H), 3.20-2.62 (m, 4H), 2.30-2.10 (m, 2H), 1.79 (s, 3H), 1.49 (s, 3H), 1.46 (s, 3H); Anal. Calcd for C33H37N3O5S2.1.75H2O: C, 60.86; H, 6.27; N, 6.45. Found: C, 60.57; H, 5.90; N, 6.32.

EXAMPLE A20

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid cyclopropylmethyl-amide

[0535]

151

[0536]

1
H NMR (DMSO-d6) δ 9.32, (s, 1H), 8.08 (d, J=8.4, 1H), 7.98 (t, J=6.0, 1H), 7.33 (d, J=6.9, 2H), 7.24 (t, J=7.2, 2H), 7.16 (t, J=7.1, 1H), 6.94 (t, J=7.8, 1H), 6.88 (d, J=7.1, 1H), 6.55 (d, J=6.6, 1H), 5.09 (d, J=9.1, 1H), 5.00 (d, J=9.1, 1H), 4.46 (d, J=3.4, 1H), 4.41 (s, 1H), 4.40 (m, 1H), 2.95 (m, 2H), 2.87-2.65 (m, 2H), 1.82 (s, 3H), 1.50 (s, 3H), 1.38 (s, 3H), 0.89 (m, 1H), 0.38 (m, 2H), 0.16 (m, 2H); HRMS (ESI) m/z calcd for C27H35N3O5SNa (M+Na)+ 548.2190, found 548.2180.

EXAMPLE A21

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid cyclohexylamide

[0537]

152

[0538]

1
H NMR (DMSO-d6) δ 9.33, (s, 1H), 8.18 (d, J=8.4, 1H), 7.79 (d, J=8.0, 1H), 7.35-7.12 (m, 5H), 6.92 (t, J=7.9, 1H), 6.75 (d, J=8.1, 1H), 6.53 (d, J=7.5, 1H), 5.29 (d, J=7.0, 1H), 5.09 (d, J=9.2, 1H), 5.00 (d, J=9.2, 1H), 4.56-4.37 (m, 2H), 3.61-3.49 (m, 2H), 2.89-2.65 (m, 2H), 1.80 (s, 3H), 1.79-1.58 (m, 5H), 1.48 (s, 3H), 1.36 (s, 3H), 1.35-1.02 (m, 5H); Anal. Calcd for C30H39N3O5S: C, 65.07; H, 7.10; N, 7.59. Found: C, 65.39; H, 6.92; N, 7.32.

EXAMPLE A22

3-(2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic acid-(4-methyl-pyridin-3-ylmethyl) Amide

[0539]

153

[0540]

1
H NMR (DMSO-d6) δ 9.33 (s, 1H), 8.43 (s, 1H), 8.39 (t, J=6.0, 1H), 8.29 (d, J=4.9, 1H), 8.11 (d, J=8.2, 1H), 7.31 (d, J=7.0, 2H), 7.24 (d, J=7.0, 2H), 7.17 (m, 2H), 6.95 (t, J=7.7, 1H), 6.78 (d, J=9=7.3, 1H), 6.55 (d, J=7.0, 1H), 5.42 (d, J=6.7, 1H), 5.14 (d, J=9.1, 1H), 5.01 (d, J=9.2, 1H), 4.54-4.40 (m, 4H), 4.17 (dd, J=5.1, 15.1, 1H), 2.82 (dd, J=3.0, 14.1, 1H), 2.72 (dd, J=10.1, 14.2, 1H), 2.30 (s, 3H), 1.82 (s, 3H), 1.49 (s, 3H), 1.32 (s, 3H); Anal. Calcd for C31H36N4O5S.2H2O: C, 60.76; H, 6.58; N, 9.14; S, 5.23. Found: C, 60.89; N, 6.26; H, 8.90; S, 5.05.

EXAMPLE A23

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (thiophen-2-ylmethyl)-amide

[0541]

154

[0542]

1
H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.51 (t, J=6.0, 1H), 8.08 (d, J=8.4, 1H), 7.40-7.12 (m, 6H), 7.04-6.88 (m, 3H), 6.80 (d, J=7.4, 1H), 6.57 (d, J=7.4, 1H), 5.12 (d, J=9.0, 1H), 5.02 (d, J=9.0, 1H), 4.58-4.30 (m, 5H), 2.97-2.67 (m, 2H), 1.84 (s, 3H), 1.50 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C29H33N3O5S2Na (M+Na)+ 590.1754, found 590.1762; Anal. Calcd for C29H33N3O5S2.0.5H2O, 0.2 TFA: C, 58.90; H, 5.75; N, 7.01. Found: C, 58.85; N, 5.71; H, 6.95.

EXAMPLE A24

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (5-chloro-benzo[b]thiophen-3-ylmethyl)-amide

[0543]

155

[0544] IR (neat, cm−1) 3401, 1643, 1531, 1443, 1284, 1H NMR (DMSO-d6) δ 937 (s, 1H, 8.54 (t, J=5.7, 1H), 8.16 (d, J=8.4, 1H), 8.00-7.95 (m, 2H), 7.67 (s, 1H), 7.38 (dd, J=8.6, 2.0, 1H), 7.3)2-7.11 (m, 5H), 6.97 (t, J=7.7, 1H), 6.77 (d, J=7.9, 1H), 6.55 (d, J=7.1, 1H), 5.46 (s br, 1H), 5.14 (d, J=9.3, 1H), 5.02 (d, J=9.5, 1H), 4.62-4.40 (m, 5H), 2.87-2.67 (m, 2H), 1.82 (s, 3H), 1.47 (s, 3H), 1.30 (s, 3H); HRMS (ESI) m/z calcd for C33H34N3O5S2ClNa (M+Na)+ 674.1521, found 674.1547; Anal. Calcd for C33H34ClN3O5S2.H2O: C, 59.13; H, 5.41; N, 6.27. Found: C, 59.19; H, 5.41; N, 6.08.

EXAMPLE A25

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid Cyclopropylamide

[0545]

156

[0546]

1
H NMR (DMSO-d6) δ 9.32, (s, 1H), 8.20 (d, J=8.4, 1H), 7.80 (d, J=8.0, 1H), 7.36-7.10 (m, 5H), 6.90 (t, J=7.9, 1H), 6.75 (d, J=8.1, 1H), 6.55 (d, J=7.5, 1H), 5.35 (d, J=7.0, 1H), 5.15 (d, J=9.2, 1H), 5.02 (d, J=9.2, 1H), 4.59-4.30 (m, 3H), 2.89-2.65 (m, 3H), 1.82 (s, 3H), 1.48 (s, 3H), 1.36 (s, 3H), 0.73-0.59 (m, 2H) 0.57-0.33 (m, 2H); Anal. Calcd for C27H33N3O5S. C, 63.38; H, 6.50; N, 8.21. Found: C, 63.39; H, 6.82; N, 8.32.

EXAMPLE A26

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid Cyclobutylamide

[0547]

157

[0548]

1
H NMR (DMSO-d6) δ 9.33, (s, 1H), 8.18 (d, J=8.4, 1H), 7.79 (d, J=8.0, 1H), 7.40-7.12 (m, 5H), 6.90 (t, J=7.9, 1H), 6.75 (d, J=8.1, 1H), 6.47 (d, J=7.5, 1H), 5.34 (d, J=7.0, 1H), 5.14 (d, J=9.2, 1H), 4.99 (d, J=9.2, 1H), 4.55-4.32 (m, 3H), 2.90-2.65 (m, 3H), 1.81 (s, 3H), 1.49 (s, 3H), 1.36 (s, 3H) 1.34-1.02 (m, 6H); Anal. Calcd for C28H35N3O5S: C, 63.97; H, 6.71; N, 7.99. Found: C, 64.05; H, 6.55; N, 8.07.

EXAMPLE A27

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid Cyclopentylamide

[0549]

158

[0550]

1
H NMR (DMSO-d6) δ 9.33, (s, 1H), 8.15 (d, J=8.4, 1H), 7.80 (d, J=8.0, 1H), 7.38-7.11 (m, 5H), 6.88 (t, J=7.9, 1H), 6.75 (d, J=8.1, 1H), 6.52 (d, J=7.4, 1H), 5.30 (d, J=7.0, 1H), 5.12 (d, J=9.2, 1H), 4.99 (d, J=9.2, 1H), 4.63-4.42 (m, 3H), 2.96-2.67 (m, 3H), 1.81 (s, 3H), 1.78-1.57 (m, 4H), 1.50 (s, 3H), 1.36 (s, 3H) 1.34-1.02 (m, 4H); Anal. Calcd for C29H37N3O5S: C, 64.54; H, 6.91; N, 7.79. Found: C, 64.22; H, 6.78; N, 7.93.

EXAMPLE A28

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (2-phenyl-cyclopropyl)-amide

[0551]

159

[0552] IR (neat, cm1) 3425, 1637, 1525, 1455, 1278, 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.26(m, 1H), 8.17 (d, J=7.7, 1H), 7.36-7.05 (m, 10H), 6.93 (t, J=7.7, 1H), 6.77 (d, J=8.1, 1H), 6.54 (d, J=7.0, 1H), 5.38 (d, J=6.2, 1H), 5.12 (d, J=9.0, 1H), 5.01 (d, J=9.3, 1H), 4.49-4.36 (m, 3H), 2.84-2.68 (m, 2H), 1.92-1.82 (m, 2H), 1.81 (s, 3H), 1.50 (s, 3H), 1.37 (s, 3H), 1.22-1.09 (m, 2H); HRMS (ESI) m/z calcd for C33H37N3O5SNa (M+Na)+ 610.2346, found 610.2335; Anal. Calcd for C33H37N3O5S.0.8H2O: C, 65.82; H, 6.46; N, 6.98. Found: C, 65.77; H, 6.34; N, 6.84.

EXAMPLE A29

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (R)-indan-1-ylamide

[0553]

160

[0554] White solid: mp 128-130° C.; IR (neat, cm−1) 3306, 1632, 1537, 1454, 1286; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.37 (d, J=8.1, 1H), 8.17 (d, J=8.4, 1H), 7.38-7.06 (m, 9H), 6.93 (t, J=7.5, 1H), 6.77 (d, J=7.5, 1H), 6.54 (d, J=7.5, 1H), 5.44 (d, J=6.9, 1H), 5.35 (dd, J=16.7, 8.1, 1H), 5.15 (d, J=8.8, 1H), 5.01 (d, J=8.8, 1H), 4.58-4.32 (m, 3H), 2.95-2.70 (m, 2H), 2.40-2.20 (m, 2H), 1.90-1.70 (m, 2H), 1.81 (s, 3H), 1.51 (s, 3H), 1.43 (s, 3H); Anal. Calcd for C33H37N3O5S.0.75H2O: C, 65.92; H, 6.45; N, 6.99. Found: C, 65.57; H, 6.31; N, 6.82.

EXAMPLE A30

N-{(1S,2S)-1-Benzyl-3-[(R)-5,5-dimethyl-4-(1-morpholin-4-yl-methanoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-3-hydroxy-2-methyl-benzamide

[0555]

161

[0556] IR (neat, cm−) 3341, 2955, 1640, 1524, 1455, 1284, 1113, 1H NMR (DMSO-d6) δ 9.36(s, 1H), 8.24 (d, J=8.6, 1H,), 7.36-7.13 (m, 5H), 6.94 (t, J=7.7, 1H), 6.78 (d, J=7.5, 1H), 6.53 (d, J=7.5, 1H), 5.34 (m, 1H), 5.12 (d, J=9.2, 1H), 5.04 (d, J=9.2, 1H), 4.50 (m, 1H), 4.33-4.30 (m, 2H), 3.78-3.51 (m, 8H), 2.81-2.62 (m, 2H), 1.80 (s, 3H), 1.56 (s, 3H), 1.38 (s, 3H); HRMS (ESI) m/z calcd for NaC28H35N3O6S (M+Na)+ 564.2139, found 564.2116.

EXAMPLE A31

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid Cycloheptylamide

[0557]

162

[0558]

1
H NMR (DMSO-d6) δ 9.32, (s, 1H), 8.20 (d, J=8.4, 1H), 7.78 (d, J=8.0, 1H), 7.40-7.12 (m, 5H), 6.92 (t, J=7.9, 1H), 6.73 (d, J=8.1, 1H), 6.50 (d, J=7.5, 1H), 5.29 (d, J=7.0, 1H), 5.19 (d, J=9.2, 1H), 5.03 (d, J=9.2, 1H), 4.62-4.37 (m, 3H), 2.92-2.67 (m, 3H), 1.80 (s, 3H), 1.79-1.01 (m, 18H); Anal. Calcd for C31H41N3O5S: C, 65.58; H, 7.28; N, 7.40. Found: C, 65.74; H, 7.07; N, 7.53.

EXAMPLE A32

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-cyclohex-2-enylamide

[0559]

163

[0560] White solid: mp 177-179° C.; IR (neat, cm−1) 3319, 2943, 1637, 1531, 1455, 1361, 1284; 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.16 (d, J=7.6, 1H), 7.95 (d, J=7.7, 1H), 7.38-7.10 (m, 5H), 6.93 (t, J=7.6, 1H), 6.76 (d, J=7.6, 1H), 6.53 (d, J=7.6, 1H), 5.80-5.70 (m,1H), 5.50-5.40 (m, 1H), 5.35 (d, J=6.9, 1H), 5.11 (d, J=9.2, 1H), 4.99 (d, J=9.2, 1H), 4.55-4.30 (m, 4H), 2.84-2.62 (m, 2H), 2.00-1.62 (m, 9H), 1.48 (s, 3H), 1.37 (s, 3H); Anal. Calcd for C30H37N3O5S.0.5H2O: C, 64.26; H, 6.83; N, 7.49. Found: C, 64.21; H, 6.74; N, 7.36.

EXAMPLE A33

N-{(1S,2S)-1-Benzyl-3-[(R)-5,5-dimethyl-4-(1-thiomorpholin-4-yl-methanoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-3-hydroxy-2-methyl-benzamide

[0561]

164

[0562]

1
H NMR (DMSO-d6) δ 9.40 (s, 1H), 8.30 (d, J=8.4, 1H), 7.40-7.16 (m, 5H), 6.97 (t, J=7.5, 1H), 6.80 (d, J=8.1, 1H), 6.57 (d, J=7.1, 1H), 5.40 (d, J=7.1, 1H), 5.18 (d, J=9.2, 1H), 5.06 (d, J=9.7, 1H), 4.54 (m, 1H), 4.35-4.19 (m, 2H), 3.68-3.59 (m, 2H), 3.28-3.10 (m, 2H), 2.87-2.44 (m, 6H), 1.83 (s, 3H), 1.60 (s, 3H), 1.37 (s, 3H); HRMS (ESI) m/z calcd for C28H35N3O5S2Na (M+Na)+ 580.1910, found 580.1922.

EXAMPLE A34

N-{(1S,2S)-1-Benzyl-3-[(R)-5,5-dimethyl-4-(1-piperidin-1-yl-methanoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-3-hydroxy-2-methyl-benzamide

[0563]

165

[0564] IR (neat, cm−1) 3389, 2931, 1631, 1461, 1284, 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.05 (d, J=8.1, 1H), 7.38-7.12 (m, 5H), 6.94 (t, J=7.7, 1H), 6.77 (d, J=7.3), 1H), 6.53 (d, J=7.3, 1H), 5.29 (d, J=7.1, 1H), 5.14-5.01 (m, 2H), 4.50 (m, 1H), 4.3)2-4.19 (m, 2H), 3.78-3.67 (m, 2H), 3.42-3.09 (m, 2H), 2.81-2.62 (m, 2H), 1.80 (s, 3H), 1.75-1.35 (m, 6H), 1.57 (s, 3H), 1.36 (s, 3H); HRMS (ESI) m/z calcd for C29H37N3O5SNa (M+Na)+ 562.2346, found 562.2327; Anal. Calcd for C29H37N3O5S.0.8H2O: C, 62.86; H, 7.02; N, 7.58. Found: C, 62.83; H, 6.95; N, 7.38.

EXAMPLE A35

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-(S)-indan-1-ylamide

[0565]

166

[0566] White solid: mp 204-206° C.; IR (neat, cm−1) 3307, 1633, 1537, 1454, 1287; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.37 (d, J=8.1, 1H), 8.17 (d, J=8.4, 1H), 7.38-7.06 (m, 9H), 6.93 (t, J=7.5, 1H), 6.77 (d, J=7.5, 1H), 6.54 (d, J=7.5, 1H), 5.44 (d, J=6.9, 1H), 5.35 (dd, J=16.7, 8.1, 1H), 5.13 (d, J=8.8, 1H), 5.04 (d, J=8.8, 1H), 4.58-4.32 (m, 3H), 2.95-2.70 (m, 2H), 2.40-2.20 (m, 2H), 1.90-1.70 (m, 2H), 1.81 (s, 3H), 1.51 (s, 3H), 1.43 (s, 3H); Anal. Calcd for C33H37N3O5S: C, 67.44; H, 6.35; N, 7.15. Found: C, 67.10; H, 6.43; N, 7.02.

EXAMPLE A36

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (4-methyl-cyclohexyl)-amide

[0567]

167

[0568] White solid: mp 192-194° C.; IR (neat, cm−1) 3298, 2955, 1638, 1531, 1449, 1349, 1284, 1099; 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.22-8.21 (m, 1H), 7.82-7.70 (m, 1H), 7.34-7.14 (m, 5H), 6.95-6.90 (m, 1H), 6.76 (d, J=8.1, 1H), 6.53 (d, J=7.3, 1H), 5.33 (d, J=5.9, 1H), 5.13-4.94 (m, 2H), 4.60-4.30 (m, 3H), 3.80-3.40 (m, 1H), 2.81-2.68 (m, 2H), 1.79 (s, 3H), 1.80-1.13 (m, 15H), 0.89-0.82 (m, 3H); Anal. Calcd for C31H41N3O5S.1H2O: C, 63.57; H, 7.40; N, 7.17. Found: C, 63.73; H, 7.36; N, 6.91.

EXAMPLE A37

(R)-3-((2S,3S)-2-Hydroxy-3-(1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (tetrahydro-furan-2-ylmethyl)-amide

[0569]

168

[0570]

1
H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.14 (d, J=8.8, 1H), 8.03 (t, J=5.0, 1H), 7.32-7.15 (m, 5H), 6.94 (t, J=7.5, 1H), 6.79 (d, J=7.5, 1H), 6.57 (d, J=7.5, 1H), 5.49 (d, J=5.5, 1H), 5.12 (d, J=9.3, 1H), 5.02 (d, J=9.3, 1H), 4.52-4.12 (m, 3H), 3.79-3.53 (m, 5H), 3.31-3.20 (m, 2H); 2.92-2.62 (m, 2H), 1.90-1.71 (m, 2H), 1.69 (s, 3H), 1.48 (s, 3H), 1.34 (s, 3H); Anal. Calcd for C29H37N3O6S.0.5H2O: C, 61.68; H, 16.78; N, 7.44. Found: C, 61.52; H, 6.62; N, 7.53.

EXAMPLE A38

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (R)-cyclohex-2-enylamide

[0571]

169

[0572] White solid: mp=193-195° C.; IR (neat, cm−1) 3316, 2931, 1637, 1584, 1519, 1449, 1349, 1279, 1085; 1H NMR (DMSO-d6) δ 9.34 (s, 1H), 8.14 (d, J=8.4, 1H), 8.03 (d, J=8.1, 1H), 7.35-7.12 (m, 5H), 6.93 (t, J=7.2, 1H), 6.77 (d, J=7.2, 1H), 6.53 (d, J=7.2, 1H), 5.79(d, J=9.9, 1H), 5.52 (d, J=9.9, 1H), 5.36 (d, J=6.8, 1H), 5.10 (d, J=9.2, 1H), 4.99 (d, J=9.2, 1H), 4.48-4.20 (m, 4H), 2.84-2.62 (m, 2H), 2.00-1.85 (m, 2H), 1.80 (s, 3H), 1.80-1.40 (m, 4H), 1.48 (s, 3H), 1.37 (s, 3H); Anal. Calcd for C30H37N3O5S.0.25H2O: C, 64.60; H, 6.78; N, 7.53. Found: C, 64.83; H, 6.72; N, 7.44.

EXAMPLE A39

(R)-3-((2S,3S)-2-Hydroxy-3-{1[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (cyclopent-1-enylmethyl)-amide

[0573]

170

[0574]

1
H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.11 (d, J=7.9, 1H), 8.06 (t, J=5.7, 1H), 7.33-7.13 (m, 5H), 6.94 (t, J=7.7, 1H), 6.77 (d, J=8.1, 1H), 6.53 (d, J=7.5, 1H), 5.50 (s, 1H), 5.45 (d, J=6.6, 1H), 5.11 (d, J=9.0, 1H), 4.98 (d, J=9.2, 1H), 4.47-4.38 (m, 3H), 3.81 (dd, J=15.8, 6.4, 1H), 3.61 (dd, J=15.9, 5.3, 1H), 2.84-2.67 (m, 2H), 2.20-2.15 (m, 4H), 1.83-1.73 (m, 2H), 1.80 (s, 3H), 1.49 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C30H37N3O5SNa (M+Na)+ 574.2346, found 574.2354.

EXAMPLE A40

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (thiophen-3-ylmethyl)-amide

[0575]

171

[0576]

1
H NMR (DMSO-d6) δ 9.40 (s, 1H), 8.44 (t, J=5.7, 1H), 8.16 (d, J=8.1, 1H), 7.45 (m, 1H), 7.35-7.15 (m, 6H), 7.05 (d, J=6.0, 1H), 6.97 (t, J=7.7, 1H), 6.80 (d, J=8.1, 1H), 6.57 (d, J=7.3, 1H), 5.52 (d, J=6.4, 1H), 5.15 (d, J=9.3, 1H), 5.03 (d, J=9.2, 1H), 5.12-4.37 (m, 4H), 2.86-2.67 (m, 2H), 4.18 (dd, J=15.2, 5.1, 1H), 2.89-2.70 (m, 2H), 1.84 (s, 3H), 1.52 (s, 3H), 1.36 (s, 3H); HRMS (ESI) m/z calcd for C29H33N3O5S2Na (M+Na)+ 590.1754, found 590.1734; Anal. Calcd for C29H33N3O5S2.0.6H2O: C, 60.20; H, 5.96; N, 7.26. Found: C, 60.26; H, 6.02; N, 7.08.

EXAMPLE A41

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (thiazol-2-ylmethyl)-amide

[0577]

172

[0578]

1
H NMR (DMSO-d6) δ 9.38 (s, 1H), 8.82 (t, J=5.9, 1H), 8.11 (d, J=8.2, 1H), 7.68 (d, J=3.3, 1H), 7.57 (d, J=3.1, 1H), 7.33-7.13 (m, 5H), 6.94 (t, J=7.7, 1H), 6.77 (d, J=7.3, 1H), 6.54 (d, J=6.6, 1H), 5.49 (d, J=6.4, 1H), 5.11 (d, J=9.3, 1H), 5.02 (d, J=9.3, 1H), 4.64-4.38 (m, 5H), 2.88-2.68 (m, 2H), 1.82 (s, 3H), 1.51 (s, 3H), 1.36 (s, 3H); HRMS (ESI) m/z calcd for C28H32N4O5S2Na (M+Na)+ 591.1706, found 591.1710.

EXAMPLE A42

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (5,6,7,8-tetrahydro-quinolin-5-yl)-amide

[0579]

173

[0580] Purified by Prep HPLC using 15% CH3CN/H2O (0.1% TFA) to 95% CH3CN at 254 nm. White foam; IR (cm−1) 3298, 2943, 1637, 1584, 1531, 1447, 1366; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.34-8.28 (m, 2H), 8.20 (d, J=8.6, 1H), 7.55 (d, J=6.9, 1H), 7.27-6.90 (m, 7H), 6.76 (d, J=8.1, 1H), 6.53 (d, J=7.5, 1H), 5.37 (d, J=6.7, 1H), 5.10-5.00 (m, 1H), 5.14 (d, J=9.3, 1H), 5.01 (d, J=9.3, 1H), 4.58-4.40 (m, 2H),), 4.40 (s, 1H), 2.90-2.60 (m, 2H), 2.00-1.80 (m, 6H), 1.79 (s, 3H), 1.49 (s, 3H), 1.42 (s, 3H); Anal. Calcd for C33H38N4O5S.0.5 TFA.0.6H2O: C, 60.90; H, 5.97; N, 8.36. Found: C, 60.87; H, 6.28; N, 8.44.

EXAMPLE A43

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (5,6,7,8-tetrahydro-quinolin-5-yl)-amide

[0581]

174

[0582] Purified by Prep HPLC using 15% CH3CN/H2O (0.1% TFA) to 95% CH3CN at 254 mm. White foam; IR (cm−) 3298, 2942, 1637, 1584, 1531, 1447, 1366, 1208, 1091; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.47 (d, J=8.8, 1H), 8.30 (dd, J=4.8, 1.2, 1H), 8.18 (d, J=8.4, 1H), 7.63 (d, J=7.2, 1H), 7.37-6.90 (m, 7H), 6.76 (d, J=8.1, 1H), 6.55 (d, J=7.5, 1H), 5.45 (d, J=6.9, 1H), 5.50-5.05 (m, 1H), 5.16 (d, J=8.9, 1H), 5.01 (d, J=8.9, 1H), 4.52-4.49 (m, 2H),), 4.42 (s, 1H), 3.00-2.65 (m, 2H), 2.00-1.60 (m, 6H), 1.80 (s, 3H), 1.50 (s, 3H), 1.42 (s, 3H); Anal. Calcd for C33H38N4O5S.0.5 TFA.0.6H2O: C, 60.90; H, 5.97; N, 8.36. Found: C, 60.87; H, 6.28; N, 8.44.

EXAMPLE A44

3-(2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (1H-indazol-3-ylmethyl)-amide

[0583]

175

[0584]

1
H NMR (DMSO-d6) δ 12.81 (s, 1H), 9.34 (s, 1H), 8.51 (t, J=5.5, 1H), 8.14 (d, J=8.2, 1H) 7.86-6.56 (m, 12H), 5.35 (d, J=6.6, 1H), 5.12 (d, J=9.1, 1H), 5.03 (d, J=9.1, 1H), 4.74-4.41 (m, 5H), 4.49 (s, 1H), 2.91-2.69 (m, 2H), 1.84 (s, 3H), 1.47 (s, 3H), 1.30 (s, 3H); Anal. Calcd for C32H35N5O5S.0.5 EtOAc: C, 63.23; H, 6.09; N, 10.85; S, 4.97. Found: C, 63.12; H, 6.27; N, 10.78; S, 4.86.

EXAMPLE A45

(R)-3-((2S,3S)-2-Hydroxy-3-{1[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (furan-3-ylmethyl)-amide

[0585]

176

[0586]

1
H NMR (DMSO-d6) δ 9.40 (s, 1H), 8.34 (t, J=5.7, 1H), 8.18 (d, J=8.4, 1H), 7.57 (m, 2H), 7.36-7.15 (m, 5H), 6.97 (t, J=7.7, 1H), 6.80 (d, J=7.9, 1H), 6.57 (d, J=7.3, 1H), 6.41 (s, 1H), 5.47 (d, J=6.2, 1H), 5.12 (d, J=9.2, 1H), 5.00 (d, J=9.2, 1H), 4.46-4.39 (m, 3H), 4.22-3.98 (m, 2H), 2.85-2.67 (m, 2H), 1.81 (s, 3H), 1.48 (s, 3H), 1.32 (s, 3H); HRMS (ESI) m/z calcd for C29H34N3O6S (M+H)+ 552.2168, found 551.2173; Anal. Calcd for C29H33N3O6S: C, 61.63; H, 6.15; N, 7.43. Found: C, 61.76; H, 6.10; N, 7.24.

EXAMPLE A46

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (tetrahydro-furan-3-ylmethyl)-amide

[0587]

177

[0588]

1
H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.14-8.03 (m, 2H), 7.34-7.13 (m, 5H), 6.93 (t, J=7.9, 1H), 6.76 (d, J=8.1, 1H), 6.52 (d, J=7.5, 1H), 5.43 (m, 1H), 5.10 (d, J=9.3, 1H), 4.99 (d, J=9.2, 1H), 4.46-4.35 (m, 3H), 3.69-3.50 (m, 4H), 3.40-3.22 (m, 1H), 3.12-2.95 (m, 2H), 2.84-2.66 (m, 2H), 2.36-2.27 (m, 1H), 1.87-1.76 (m, 1H), 1.80 (s, 3H), 1.49 (s, 3H), 1.34 (s, 3H); HRMS (ESI) m/z calcd for C29H37N3O6SNa (M+Na)+ 556.2470, found 556.2481; Anal. Calcd for C29H37N3O6S.0.75H2O: C, 61.19; H, 6.72; N, 7.38. Found: C, 61.24; H, 6.59; N, 7.01.

EXAMPLE A47

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (4,5,6,7-tetrahydro-benzofuran-4-yl)-amide

[0589]

178

[0590] White foam; IR (cm−) 3331, 2943, 1643, 1590, 1522, 1445, 1364, 1282; 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.21-8.16 (m, 2H), 7.42-7.14 (m, 6H), 6.96-6.90 (m, 1H), 6.76 (d, J=8.2, 1H), 6.54 (d, J=7.2, 1H), 6.28 (d, J=1.8, 1H), 5.39 (d, J=6.9, 1H), 5.13 (d, J=9.0, 1H), 5.02 (d, J=9.0, 1H), 4.90-4.70 (m, 1H), 4.55-4.30 (m, 3H), 2.89-2.68 (m, 2H), 1.81 (s, 3H), 2.00-1.50 (m, 6H), 1.48 (s, 3H), 1.39 (s, 3H); Anal. Calcd for C32H37N3O6S.0.5H2O: C, 63.98; H, 6.38; N, 6.99. Found: C, 63.93; H, 6.44; N, 6.68.

EXAMPLE A48

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (4,5,6,7-tetrahydro-benzofuran-4-yl)-amide

[0591]

179

[0592] White foam; IR (cm−1) 3316, 2935, 1754, 1657, 1642, 1584, 1530, 1454, 1357, 1284, 1209; 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.19 (d, J=8.8, 1H), 8.14 (d, J=8.1, 1H), 7.43-7.14 (m, 6H), 6.96-6.91 (m, 1H), 6.77 (d, J=7.9, 1H), 6.54 (d, J=7.5, 1H), 6.38 (d, J=1.9, 1H), 5.32 (d, J=6.9, 1H), 5.13 (d, J=9.0, 1H), 5.00 (d, J=9.0, 1H), 4.83-4.50 (m, 1H), 4.52-4.12 (m, 3H), 2.82-2.62 (m, 2H), 1.79 (s, 3H), 2.00-1.50 (m, 6H), 1.47 (s, 3H), 1.41 (s, 3H); Anal. Calcd for C32H37N3O6S.0.5H2O: C, 63.98; H, 6.38; N, 6.99. Found: C, 64.03; H, 6.37; N, 6.66.

EXAMPLE A49

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (4,5,6,7-tetrahydro-benzo[b]thiophen-4-yl)-amide

[0593]

180

[0594] White foam; IR (cm−) 3317, 2943, 1643, 1525, 1455, 1367, 1256; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.36 (d, J=8.6, 1H), 8.18 (d, J=8.2, 1H), 7.37 (d, J=7.2, 1H), 7.28-6.75 (m, 8H), 6.54 (d, J=7.2, 1H), 5.41 (d, J=6.9, 1H), 5.14 (d, J=8.8, 1H), 4.99 (d, J=8.8, 1H), 5.00-4.56 (m, 1H),), 4.52-4.30 (m, 3H), 2.80-2.60 (m, 2H), 1.81 (s, 3H), 2.00-1.60 (m, 6H), 1.49 (s, 3H), 1.41 (s, H); Anal. Calcd for C32H37N3O5S2.0.5H2O: C, 62.31; H, 6.21; N, 6.81. Found: C, 62.30; H, 6.17; N, 6.60.

EXAMPLE A50

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (4,5,6,7-tetrahydro-benzo[b]thiophen-4-yl)-amide

[0595]

181

[0596] White foam; IR (cm−) 3321, 2935, 1642, 1585, 1530, 1372, 1283, 1045; 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.24 (d, J=8.8, 1H), 8.20 (d, J=8.4, 1H), 7.31 (d, J=7.2, 1H), 7.23-6.70 (m, 8H), 6.54 (d, J=7.2, 1H), 5.32 (d, J=6.4, 1H), 5.13 (d, J=9.2, 1H), 5.01 (d, J=9.2, 1H), 5.00-4.60 (m, 1H), 4.60-4.30 (m, 3H), 2.80-2.60 (m, 2H), 1.80 (s, 3H), 2.00-1.60 (m, 6H), 1.47 (s, 3H), 1.42 (s, 3H); Anal. Calcd for C32H37N3O5S2: C, 63.24; H, 6.14; N, 6.91. Found: C, 63.59; H, 6.20; N, 6.68.

EXAMPLE A51

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (6,7-dihydro-5H-[1]pyrindin-5-yl)-amide

[0597]

182

[0598] Purified by Prep HPLC using 15% CH3CN/H2O (0.1% TFA) to 95% CH3CN at 254 nm. White foam; IR (cm−1) 3296, 2966, 1644, 1538, 1554, 1373, 1284, 1046; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.41 (d, J=7.3, 1H), 8.33 (d, J=4.4, 1H), 8.19 (d, J=9.2, 1H), 7.55 (d, J=7.2, 1H), 7.36 (d, J=7.2, 1H), 7.28-6.90 (m, 6H), 6.76 (d, J=7.9, 1H), 6.53 (d, J=6.6, 1H), 5.39 (d, J=7.2, 1H), 5.32 (dd, J=14.9, 7.3, 1H), 5.15 (d, J=9.0, 1H), 5.02 (d, J=9.0, 1H), 4.54-4.34 (m, 3H), 3.00-2.60 (m, 4H), 2.44-2.30 (m, 1H), 1.98-1.81 (m, 1H), 1.79 (s, 3H), 1.48 (s, 3H), 1.40 (s, 3H); Anal. Calcd for C32H36N4O5S.0.25 TFA.0.5H2O: C, 62.33; H, 6.00; N, 8.95. Found: C, 62.58; H, 6.15; N, 8.95.

EXAMPLE A52

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (6,7-dihydro-5H-[1]pyrindin-5-yl)-amide

[0599]

183

[0600] Purified by Prep HPLC using 15% CH3CN/H2O (0.1% TFA) to 95% CH3CN at 254 nm. White foam; IR (cm−) 3296, 2966, 1643, 1539, 1554, 1373, 1284, 1045; 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.59 (d, J=8.0, 1H), 8.32 (d, J=4.0, 1H), 8.16 (d, J=8.4, 1H), 7.57 (d, J=7.7, 1H), 7.36 (d, J=7.7, 1H), 7.25-6.90 (m, 6H), 6.76 (d, J=8.0, 1H), 6.54 (d, J=7.7, 1H), 5.43 (d, J=6.9, 1H), 5.36 (dd, J=16.0, 8.0, 1H), 5.14 (d, J=9.0, 1H), 5.01 (d, J=9.0, 1H), 4.54-4.36 (m, 3H), 2.90-2.70 (m, 4H), 2.44-2.30 (m, 1H), 1.84-1.70 (m, 1H), 1.80 (s, 3H), 1.51 (s, 3H), 1.42 (s, 3H); Anal. Calcd for C32H36N4O5S.0.25 TFA.0.5H2O: C, 62.33; H, 6.00; N, 8.95. Found: C, 62.41; H, 6.38; N, 8.81.

EXAMPLE A53

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (2-methyl-furan-3-ylmethyl)-amide

[0601]

184

[0602]

1
H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.20 (m, 1H), 8.14 (d, J=7.9, 1H), 7.35-7.13 (m, 6H), 6.94 (t, J=7.7, 1H), 6.75 (d, J=8.0, 1H), 6.53 (d, J=7.5, 1H), 6.28 (s, 1H), 5.42 (d, J=6.6, 1H), 5.11 (d, J=9.0, 1H), 4.99 (d, J=9.1, 1H), 4.46-4.38 (m, 3H), 4.12-3.92 (m, 2H), 2.84-2.66 (m, 2H), 2.20 (s, 3H), 1.80 (s, 3H), 1.46 (s, 3H), 1.30 (s, 3H); HRMS (ESI) m/z calcd for C30H36N3O6S (M+H)+ 566.2332, found 566.2325.; Anal. Calcd for C30H35N3O6S.0.5H2O: C, 62.70; H, 6.31; N, 7.31. Found: C, 62.82; H, 6.19; N, 7.09.

EXAMPLE A54

(R)-3-[(2S,3S)-2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (3-methyl-benzofuran-2-ylmethyl)-amide

[0603]

185

[0604]

1
H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.55 (t, J=5.5, 1H), 8.15 (d, J=8.3, 1H), 7.52 (d, J=6.9, 1H, 7.51-7.36 (m, 3H), 7.28-7.18 (m, 5H), 6.96 (t, J=7.8, 1H), 6.78 (d, J=8.0, 1H), 6.55 (d, J=7.4, 1H), 5.42 (br s, 1H), 5.12 (d, J=9.1, 1H), 5.00 (d, J=9.1, 1H), 4.48-4.39 (m, 5H), 2.83 (m, 1H), 2.72 (dd, J=13.5, 10.7, 1H), 2.20 (s, 3H), 1.99 (s, 3H), 1.46 (s, 3H), 1.27 (s, 3H); HRMS (ESI) m/z calcd for C34H38N3O6S (M+H)+ 616.2481, found 616.2464; Anal. Calcd for C34H37N3O6S: C, 66.32; H, 6.06; N, 6.82. Found: C, 60.06; H, 6.04; N, 6.71.

EXAMPLE A55

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid ((S)-6,8-difluoro-chroman-4-yl)-amide

[0605]

186

[0606] White solid: 1H NMR (DMSO) δ 9.36 (s, 1H), 8.49 (d, J=8.1, 1H), 8.21 (d, J=8.6, 1H), 7.30-6.50 (m, 10H), 5.34 (d, J=6.2, 1H), 5.16 (d, J=9.3, 1H), 5.10-4.90 (m, 2H), 4.55-4.20 (m, 3H), 2.80-2.60 (m, 2H), 2.10-1.95 (m, 2H), 1.78 (s, 3H), 1.50 (s, 3H), 1.43 (s, 3H), 1.40-1.35 (m, 1H), 1.30-1.20 (m, 1H); HRMS (ESI) m/z calcd for C33H36N3O6F2S (M+H)+ 640.2293, found 640.2284.

EXAMPLE A56

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid ((S)-5-fluoro-indan-1-yl)-amide

[0607]

187

[0608] White solid: 1H NMR (DMSO) δ 9.36 (s, 1H), 8.33 (d, J=7.8, 1H), 8.20 (d, J=8.6, 1H), 7.30-6.50 (m, 1H), 5.37 (d, J=6.9, 1H), 5.30-5.20 (m, 1H), 5.14 (d, J=8.9, 1H), 5.02 (d, J=8.9, 1H), 4.60-4.30 (m, 3H), 3.00-2.60 (m, 4H), 2.50-2.30 (m, 1H), 2.00-1.80 (m, 1H), 1.19 (s, 3H), 1.48 (s, 3H), 1.41 (s, 3H).; HRMS (ESI) m/z calcd for C33H37N3O5FS (M+H)+ 606.2438, found 606.2441.

EXAMPLE A57

N-{(1S,2S)-1-Benzyl-3-[(R)-5,5-dimethyl-4-(N′-methyl-N′-phenyl-hydrazinocarbonyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-3-hydroxy-2-methyl-benzamide

[0609]

188

[0610]

1
H NMR (DMSO-d6) δ 10.12 (s, 1H), 9.37 (s, 1H), 8.18 (d, 1H, J=8.2), 7.26-7.11 (m, 7H), 6.96-6.87 (m, 3H), 6.77 (d, 1H, J=7.3), 6.68 (t, 1H, J=7.1), 6.54 (d, 1H, J=7.5), 5.55 (d, 1H, J=6.6), 5.16 (d, 1H, J=9.3), 5.04 (d, 1H, J=9.2), 4.48 (d, 1H, J=4.5), 4.42-4.32 (m, 1H), 4.40 (s, 1H), 3.05 (s, 3H), 2.86-2.68 (m, 2H), 1.81 (s, 3H), 1.55 (s, 3H), 1.47 (s, 3H). Exact mass calculated for C31H37N4O5S (M+H)+ 577.2485, found 577.2469.

EXAMPLE A58

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiiazolidine-4-carboxylic Acid (ethyl-morpholino)-amide

[0611]

189

[0612] White solid: 1H NMR (DMSO-d6) δ 9.81, (s 1H), 9.40 (s, 1H), 8.18 (s, 1H), 7.41-6.91 (m, 10H), 6.62 (d, J=7.7, 1H), 5.12 (q, J=9.3, 1H), 4.44-4.35 (m, 3H), 4.08-2.78 (m, 12H), 2.81-2.67 (m, 2H), 1.88 (s, 3H), 1.49 (s, 3H), 1.34 (s, 3H); Anal. (C30H40N4O6S.1.0H2O.0.5 TFA) calculated C, (56.13); H, (6.45); N, (8.42). found C, (56.31); H, (6.55); N, (7.83). HRMS (ESI) m/z calcd for 585.2740, found 585.2747.

EXAMPLE A59

(R)-3-((2S,3S)-2-Hydroxy-3-{1[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (2,2-difluoro-benzo[1,3]dioxol-5-ylmethyl)-amide

[0613]

190

[0614]

1
H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.55 (t, J=5.8, 1H), 8.14 (d, J=8.4, 1H), 7.29-7.11 (m, 8H), 6.94 (t, J=7.8, 1H), 6.77 (d, J=7.9, 1H), 6.54 (d, J=7.4, 1H), 5.58 (d, J=8.2, 1H), 5.17 (d, J=9.2, 1H), 5.02 (d, J=9.2, 1H), 4.49-4.39 (m, 3H), 4.43 (s, 1H), 4.21 (dd, J=5.4, 15.3, 1H), 2.83 (m, 1H), 2.71 (dd, J=13.5, 10.7, 1H), 2.20 (s, 3H), 1.51 (s, 3H), 1.34 (s, 3H); HRMS (ESI) m/z calcd for C32H34F2N3O7S (M+H)+ 642.2086, found 642.2099; Anal. Calcd for C32H33F2N3O7S: C, 59.90; H, 5.18; N, 6.55. Found: C, 60.01; H, 5.27; N, 6.29.

EXAMPLE A60

(R)-3-[(2S,3S)-2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (1H-benzoimidazol-2-ylmethyl)-amide

[0615]

191

[0616]

1
H NMR (D M SO-d6) δ 9.37 (s, 1H), 8.72 (t, J=5.5, 1H), 8.18 (d, J=8.3, 1H), 7.33-7.11 (m, 10H), 6.95 (t, J=7.9, 1H), 6.79 (d, J=8.1, 1H), 6.57 (d, J=7.1, 1H), 5.54 (d, J=6.6, —1H), 5.14 (d, J=9.3, 1H), 5.05 (d, J=9.3, 1H), 4.75 (m, 1H), 4.55-4.28 (m, 3H), 4.09 (dd, J=10.4, 5.2, 1H), 2.86 (m, 1H), 2.72 (dd, J=13.5, 10.7, 1H), 1.82 (s, 3H), 1.53 (s, 3H), 1.36 (s, 3H); HRMS (ESI) m/z calcd for C32H36N5O5S (M+H)+ 602.2437, found 602.2424; Anal. Calcd for C32H35N5O5S.0.4H2O: C, 63.12; H, 5.93; N, 11.50. Found: C, 63.02; H, 5.99; N, 11.49.

EXAMPLE A61

(R)-3-[(2S,3S)-2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (1H-indol-2-ylmethyl)-amide

[0617]

192

[0618]

1
H NMR (DMSO-d6) δ 10.74 (s, 1H), 9.39 (s, 1H), 8.46 (t, J=4.9, 1H), 8.17 (d, J=8.3, 1H), 7.45 (d, J=7.7, 1H), 7.37 (t, J=7.9, 2H), 7.26 (t, J=7.1, 2H), 7.18 (d, J=7.2, 1H), 7.10 (t, J=7.2, 1H), 6.99 (d, J=7.6, 1H), 6.95 (d, J=7.5, 1H), 6.79 (d, J=7.7, 1H), 6.57 (d, J=7.1, 1H), 6.41 (s, 1H), 5.49 (br s, 1H), 5.15 (d, J=9.1, 1H), 5.02 (d, J=9.2, 1H), 4.69-4.39 (m, 4H), 2.86 (m, 1H), 2.74 (dd, J=13.5, 10.6, 1H), 1.83 (s, 3H), 1.50 (s, 3H), 1.38 (s, 3H); HRMS (ESI) m/z calcd for C33H37N4O5S (M+H)+ 601.2485, found 605.2460.

EXAMPLE A62

(R)-3-[(2S,3S)-2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (benzofuran-2-ylmethyl)-amide

[0619]

193

[0620]

1
H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.55 (t, J=5.5, 1H), 8.15 (d, J=8.3, 1H), 7.52 (d, J=6.9, 1H), 7.51-7.36 (m, 3H), 7.28-7.18 (m, 5H), 6.96 (t, J=7.8, 1H), 6.78 (d, J=8.0, 1H), 6.61 (s, 1H), 6.55 (d, J=7.4, 1H), 5.42 (br s, 1H), 5.12 (d, J=9.1, 1H), 5.00 (d, J=9.1, 1H), 4.48-4.39 (m, 5H), 2.83 (m, 1H), 2.72 (dd, J=13.5, 10.7, 1H), 1.99 (s, 3H), 1.46 (s, 3H), 1.27 (s, 3H); HRMS (ESI) m/z calcd for C33H36N3O6S (M+H)+ 602.2325, found 602.2326.

EXAMPLE A63

(R)-3-[(2S,3S)-2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (1-methyl-1H-indol-2-ylmethyl)-amide

[0621]

194

[0622]

1
H NMR (DMSO-d6) δ 9.39 (s, 1H), 8.46 (t, J=4.9, 1H), 8.17 (d, J=8.3, 1H), 7.45 (d, J=7.7, 1H), 7.37 (t, J=7.9, 2H), 7.26 (t, J=7.1, 2H), 7.18 (d, J=7.2, 1H), 7.10 (t, J=7.2, 1H), 6.99 (d, J=7.6, 1H), 6.95 (d, J=7.5, 1H), 6.79 (d, J=7.7, 1H), 6.57 (d, J=7.1, 1H), 6.41 (s, 1H), 5.49 (br s, 1H), 5.15 (d, J=9.1, 1H), 5.02 (d, J=9.2, 1H), 4.66 (dd, J=15.5, 6.4, 1H), 4.49 (s, 1H), 4.44 (m, 1H), 4.34 (dd, J=15.5, 4.2, 1H), 3.67 (s, 3H), 2.86 (m, 1H), 2.74 (dd, J=13.5, 10.6, 1H), 1.83 (s, 3H), 1.50 (s, 3H), 1.38 (s, 3H); HRMS (ESI) m/z calcd for C34H39N4O5S (M+H)+ 615.2641, found 615.2628; Anal. Calcd for C34H38N4O5S.0.3H2O: C, 65.85; H, 6.27; N, 9.03. Found: C, 65.80; H, 6.23; N, 8.91.

EXAMPLE A64

(R)-3-[(2S,3S)-2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (3-methyl-benzofuran-2-ylmethyl)-amide

[0623]

195

[0624]

1
H NMR (DMSO-d6) δ 9.3)7 (s, 1H), 8.55 (t, J=5.5, 1H), 8.15 (d, J=8.3), 1H), 7.52 (d, J=6.9, 1H, 7.51-7.36 (m, 3H), 7.28-7.18 (m, 5H), 6.96 (t, J=7.8, 1H), 6.78 (d, J=8.0, 1H), 6.55 (d, J=7.4, 1H), 5.42 (br s, 1H), 5.12 (d, J=9.1, 1H), 5.00 (d, J=9.1, 1H), 4.48-4.39 (m, 5H), 2.83 (m, 1H), 2.72 (dd, J=13.5, 10.7, 1H), 2.20 (s, 3H), 1.99 (s, 3H), 1.46 (s, 3H), 1.27 (s, 3H); HRMS (ESI) m/z calcd for C34H38N3O6S (M+H)+ 616.2481, found 616.2464; Anal. Calcd for C34H37N3O6S: C, 66.32; H, 6.06; N, 6.82. Found: C, 60.06; H, 6.04; N, 6.71.

EXAMPLE A64

(R)-3-[(2S,3S)-2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid (3-methyl-benzofuran-2-ylmethyl)-amide

[0625]

196

[0626]

1
H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.55 (t, J=5.5, 1H), 8.15 (d, J=8.3, 1H), 7.52 (d, J=6.9, 1H, 7.51-7.36 (m, 3H), 7.28-7.18 (m, 5H), 6.96 (t, J=7.8, 1H), 6.78 (d, J=8.0, 1H), 6.55 (d, J=7.4, 1H), 5.42 (br s, 1H), 5.12 (d, J=9.1, 1H), 5.00 (d, J=9.1, 1H), 4.48-4.39 (m, 5H), 2.83 (m, 1H), 2.72 (dd, J=13.5, 10.7, 1H), 2.20 (s, 3H), 1.99 (s, 3H),

EXAMPLE A65

3-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiiazolidine-4-carboxylic Acid (propyl-morpholino)-amide

[0627]

197

[0628] White solid: 1H NMR (DMSO-d6) δ 9.81, (s 1H), 9.40 (s, 1H), 8.18 (s, 1H), 7.41-6.91 (m, 10H), 6.62 (d, J=7.7, 1H), 5.12 (dd, J=9.3, 1H), 4.44-4.35 (m, 3H), 4.08-2.78 (m, 13H), 2.81-2.67 (m, 2H), 1.88 (s, 3H), 1.49 (s, 3H), 1.34 (s, 3H); Anal. (C31H42N4O6S.0.18H2O) calculated C, (51.56); H, (5.53); N, (9.36). found C, (52.05); H, (5.95); N, (6.51). HRMS (ESI) m/z calcd for 599.2902, found 599.2903.

[0629] General Method B

198

[0630] Amides of the general structure 3 (synthesized in the same manor as in the Methods A section) are coupled to boc-protected acid 15, and exposed to methane sulfonic acid to yield amines 16. Subjecting amines 16 to the reaction conditions depicted yielded a series of amides 17, carbamates 18, and ureas 19.

[0631] Synthesis of Amines of the General Type 16.

199

[0632] The title compound was prepared as follows. (R)-5,5-Dimethyl-thiazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 1 (1.95 g, 7.47 mmol) was dissolved in EtOAc (25 mL) and cooled to 0° C. Diphenyl chlorophosphate (1.71 mL, 8.23 mmol) was added followed by TEA (1.14 mL, 8.23 mmol). The reaction was stirred at 0° C. for 1 h, and treated with (S)-Cyclohex-2-enylamine (0.8 g, 8.23 mmol). The reaction mixture was stirred at room temperature overnight, then partitioned between 1N HCl (25 mL) and EtOAc (30 mL). The organic layer was washed with saturated NaHCO3, brine, dried over Na2SO4 and concentrated to a yellow oil. The resulting oil (2.54 g, 7.47 mmol) was dissolved in EtOAc (30 mL) and then cooled to 0° C. Methanesulfonic acid (2.27 mL, 33.62 mmol) was added and the solution was stirred at 0° C. for 15 minutes, then at room temperature for 4 h. The mixture was re-cooled to 0° C. and quenched with 10% Na2CO3 (30 mL) then extracted with EtOAc (30 mL). Organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo to give a yellow oil 3. The resulting yellow oil (1.86 g, 7.74 mmol) was dissolved in EtOAc (77 mL). BOC-AHPBA 4 (2.29 g, 7.74 mmol) was added followed by HOBt (1.05 g, 7.74 mmol). The mixture was stirred at room temperature 1 h, then cooled to 0° C. DCC (1.60 g, 7.74 mmol) was slowly added as solution in EtOAc (30 mL). The mixture was allowed to gradually warm to room temperature and stirred overnight. The mixture was filtered and the filtrate was washed with 1N HCl (40 mL), saturated NaHCO3 (40 mL), brine (40 mL), dried over Na2SO4 and concentrated to give a crude white solid (contaminated with DCU). The DCU was removed by flash chromatography (30% to 50% EtOAc in hexanes) to provide a white solid (4 g, 7.73 mmol), which was dissolved in EtOAc (30 mL) and then cooled to 0° C. Methanesulfonic acid (2.35 mL, 34.76 mmol) was added and the solution was stirred at 0° C. for 15 minutes, then at room temperature for 3 h. The mixture was re-cooled to 0° C. and quenched with 10% Na2CO3 (35 mL) then extracted with EtOAc (30 mL). Organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo to give a material which was recrystalized from 60% EtOAc in hexanes to provide B1 (2.41 g, 80%) as a white solid. 1H NMR (DMSO-d6) δ 8.21 (d, J=8.1, 1H), 7.31-7.17 (m, 5H), 5.80 (d, J=5.6, 1H), 5.52-5.48 (m, 2H), 5.30-5.25 (m, 2H), 4.89 (s, 2H), 4.26 (s, 1H), 4.21-4.00 (m, 3H), 3.15-2.70 (m, 2H), 2.50-2.00 (m, 2H), 2.00-1.00 (m, 4H), 1.49 (s,-3H), 1.31 (s, 3H); Anal. Calcd for C22H31N3O3S: C, 63.28; H, 7.48; N, 10.06. Found: C, 63.40; H, 7.20; N, 9.98.

[0633] The following amines 16b-k were prepared by the specific method outlined above using the requisite amine.

200

[0634]

1
H NMR (DMSO-d6) δ 8.36 (t, J=6.0, 1H), 7.36-7.14 (m, 5H), 5.70 (m, 1H), 5.34 (s br, 1H), 5.12 (d, J=17.0, 1H), 4.96-4.88 (m, 3H), 4.34 (s, 1H), 4.10 (d, J=7.0, 1H), 3.80-3.55 (m, 2N), 3.06 (d, J=13.0, 1H), 2.87 (t, J=9.0, 1H), 20.38 (dd, J=13.0, 10.0, 1H), 1.52 (s, 3N), 1.33 (s, 3N)).

201

202

[0635]

1
H NMR (DMSO-d6) δ 8.69 (t, J=5.3, 1H), 7.34-7.14 (m, 5H), 5.34 (s br, 1H), 4.90 (s, 2H), 4.29 (s, 1H), 4.08 (d, J=7.0, 1H), 3.90-3.70 (m, 2H), 3.07 (dd, J=13.4, 2.5, 1H), 2.96 (t, J=2.6, 1H), 2.88, (ddd, J=9.8, 8.0, 2.8, 1H), 2.37 (dd, J=13.2, 9.9, 1H), 1.50 (s, 3H), 1.32 (s, 3H).

203

[0636]

1
H NMR (DMSO-d6) δ 8.74 (t, J=5.4, 1H), 7.36 (m, 1H), 7.34-7.14 (m, 5H), 6.24 (m, 1H), 6.16 (d, J=3.3, 1H), 5.32 (s br, 1H), 4.90 (s, 2H), 4.32 (s, 1H), 4.30-4.10 (m, 2H), 4.07 (d, J=9.0, 1H), 3.09 (dd, J=13.1, 2.6, 1H), 2.80 (ddd, J=10.0, 8.0, 2.7, 1H), 2.33 (dd, J=13.1, 10.0, 1H), 1.50 (s, 3H), 1.28 (s, 3H).

204

[0637]

1
H NMR (DMSO-d6) δ 8.36 (t, J=5.4, 1H), 7.33-7.15 (m, 5H), 5.30 (s br, 1H), 4.90 (s, 2H), 4.30 (s, 1H), 4.09 (d, J=7.9, 1H), 3.06 (dd, J=13.2, 2.0, 1H), 3.02-2.77 (m, 3H), 2.47 (dd, J=13.4, 10.1, 1H), 1.50 (s, 3H), 1.34 (s, 3H), 0.80 (m, 1H), 0.28 (m, 2H), 0.06 (m, 2H).

205

[0638]

1
H NMR (DMSO-d6) δ 8.59 (d, J=7.3, 1H), 7.29-7.20 (m, 5H), 7.04 (d, J=6.8, 1H), 6.89 (d, J=7.2, 1H), 6.76-6.72 (m, 1H), 6.53-6.46 (m, 1H), 5.32 (d, J=5.9, 1H), 4.89 (s, 2H), 4.89-4.80 (m, 1H), 4.24 (s, 1H), 4.17-3.90 (m, 2H), 3.08-3.04 (m, 2H), 2.20-1.70 (m, 4H), 1.52 (s, 3H), 1.35 (s, 3H); Anal. Calcd for C25H31N3O4S: C, 63.94; H, 6.65; N, 8.95. Found: C, 63.76; H, 6.60; N, 8.98.

206

[0639]

1
H NMR (DMSO-d6) δ 8.37 (d, J=7.3, 1H), 7.30-6.66 (m, 9H), 5.29 (d, J=8.2, 1H), 4.86 (s, 2H), 4.86-4.80, (m, 1H), 4.23 (s, 1H), 4.05-3.97 (m, 1H), 3.08-3.04 (m, 1H), 2.70-2.40 (m, 4H), 2.20-2.00 (m, 2H), 1.70-1.55 (m, 4H), 1.52 (s, 3H), 1.36 (s, 3H); Anal. Calcd for C26H33N3O3S: C, 66.78; H, 7.11; N, 8.99. Found: C, 66.90; H, 7.01; N, 8.98.

207

[0640]

1
H NMR (DMSO-d6) δ 8.47 (d, J=8.6, 1H), 7.28-6.82 (m, 9H), 5.33 (d, J=5.9, 1H), 5.25-5.19 (m, 1H), 4.91 (d, J=9.2, 1H), 4.85 (d, J=9.2, 1H), 4.29 (s, 1H), 4.03 (d, J=8.1, 1H), 3.08-3.05 (m, 1H), 2.77-2.60 (m, 2H), 2.30-2.10 (m, 2H), 1.70-1.50 (m, 2H), 1.52 (s, 3H), 1.36 (s, 3H); Anal. Calcd for C25H31N3O3S: C, 66.20; H, 6.89; N, 9.26. Found: C, 66.35; H, 7.01; N, 8.98.

208

[0641]

1
H NMR (DMSO-d6) δ 8.35 (t, J=5.7, 1H), 7.31-7.16 (m, 5H), 5.24 (d, J=8.1, 1H), 4.92 (d, J=9.2, 1H), 4.88 (d, J=9.2, 1H), 4.31 (s, 1H), 4.09 (m, 1H), 3.83-3.51 (m, 2H), 3.42-3.31 (m, 1H), 3.23-3.07 (m, 2H), 2.99-2.91 (m, 1H), 2.86-2.79 (m, 1H), 2.34 (dd, J=13.0, 10.1, 1H), 1.80-1.42 (m, 6H), 1.50 (s, 3H), 1.31 (s, 3H).

209

[0642]

1
H NMR (DMSO-d6) δ 8.13 (t, J=5.4, 1H), 7.35-7.15 (m, 5H), 5.28 (d, J=8.1, 1H), 4.79 (m, 2H), 4.27 (s, 1H), 4.07 (t, J=7.1, 1H), 3.10-2.71 (m, 4H), 2.37 (dd, J=13.2, 9.9, 1H), 1.49 (s, 3H), 1.34 (m, 2H), 1.33 (s, 3H), 0.77 (t, J=7.4, 3H).

210

[0643] Isolated yield: 84%; MS (APCI, m/z): 461, 463 (M+H)

211

[0644] Isolated yield: 93%; MS (APCI, m/z): 464 (M+H).

212

[0645] Isolated yield: 86%; MS (APCI, m/z): 496 (M+H).

213

[0646] Isolated yield: 87%. MS-APCI (m/z+): 458.

214

[0647] Isolated yield: 45%. MS-APCI (m/z+): 341, 429.

[0648] Synthesis of Final Products of the General Type 17, 18 and 19 from 16a-k, General Methods:

[0649] Carbamate formation #1—The corresponding amine, of general structure 16, triethylamine (2 eq.) and chloroformate (1.1-1.2 eq.) were taken in dichloromethane and stirred at room temperature under nitrogen. (1.5 hr to overnight). The solvent was then removed in vacuo and the resulting residue subjected to flash silica gel chromatography or preparative HPLC to afford the desired product.

[0650] Carbamate formation #2—The corresponding alcohol was treated with phosgene (1.7 eq.) in toluene followed by diisopropylethylamine (1.1 eq.) and the amine of general structure 16. The solvent was then removed in vacuo and the resulting residue subjected to flash silica gel chromatography or preparative HPLC to afford the desired product.

[0651] Amide formation—To a solution of acid, amine 16 and HOBT in CH2Cl2 was added EDC and the solution stirred overnight at room temperature. The solution was concentrated in vacuo and the residue dissolved in ethyl acetate and a small portion of water. The solution was washed with saturated NH4Cl or 0.5N HCl (2×), saturated NaHCO3 (2×), brine (1×), dried with MgSO4 and concentrated in vacuo. The resulting residue subjected to flash silica gel chromatography or preparative HPLC to afford the desired product.

[0652] Urea formation #1-The corresponding amine and isocyanate (1.1-1.2 eq.) were taken in dichloromethane and stirred at room temperature under nitrogen. (1.5 hr to overnight). The solvent was then removed in vacuo and the resulting residue subjected to flash silica gel chromatography or preparative HPLC to afford the desired product.

[0653] Urea formation #2—The corresponding amine was dissolved in CH2Cl2 and treated with diisopropylethylamine (1.5 eq.) and phosgene (1 eq., 20% soln. in toluene) at −78° C. The resulting solution was warmed to room temperature and treated with the amine of general structure 16. The resulting residue subjected to flash silica gel chromatography or preparative HPLC to afford the desired product.

Specific Carbamate Synthesis

EXAMPLE B1

{1-Benzyl-3-[5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid tetrahydropfuran-3-yl-ester

[0654]

215

[0655] (S)-(+)-3-Hydroxytetrahydrofuran (0.11 mL, 1.37 mmol) was dissolved in toluene (1 mL) and cooled to 0° C. with magnetic stirring. To this was added Phosgene as a 20% solution in toluene (1.2 mL, 2.34 mmol). The resulting solution was stirred for 24 h at 23° C. then concentrated. The residue was dissolved in dry THF (3 mL) and treated with Diisopropylethylamine (0.25 mL, 1.40 mmol). 16c was added as a slurry in THF (0.3 g, 0.73 mmol) and resulting amber solution was stirred at 23° C. for 3 h. The solution was diluted with EtOAc (10 mL) and washed with 10% citric acid (25 mL) dried over Na2SO4, filtered, and concentrated to a white solid.

[0656]

1
H NMR (CDCl3) δ 7.23-7.09 (m, 9H), 6.79 (s br, 1H), 5.90 (s br, 1H), 5.16-3.63 (m, 17H), 1.55 (s, 3H), 1.50 (s, 3H), 1.45 (s, 3H); HRMS (ESI) m/z calcd for C29H37N3O6SNa (M+Na)+ 578.2301, found 578.2288; Anal. Calcd for C29H37N3O6S.1H2O: C, 60.71; H, 6.85; N, 7.32. Found: C, 60.97; H, 6.47; N, 6.91.

Specific Amide Synthesis

EXAMPLE B2

1,2,3,4-Tetrahydro-quinoline-5-carboxylic Acid {(1S,2S)-1-benzyl-3-[(R)-5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-amide

[0657]

216

[0658] The amine 16c (0.21 g, 0.48 mmol) and 1,2,3,4-Tetrahydroquinoline-5-carboxylic acid (0.085 g, 0.48 mmol) were dissolved in dry CH2Cl2 (5 mL) at 23° C. with magnetic stirring. The solution was treated sequentially with EDC (0.18 g, 0.96 mmol), HOBt (0.13 g, 0.96 mmol), and Triethylamine (0.14 mL, 0.96 mmol). The result was stirred for 24 h and then poured into H2O (25 mL). The mixture was extracted with EtOAc (2×25 mL). The combined organics were washed sequentially with saturated NaHCO3 (1×50 mL), 0.5N HCl (1×50 mL), and H2O (1×50 mL). The result was dried over Na2SO4, filtered, and concentrated. The residue was purified by flash column chromatography (40%-60% EtOAc in hexanes) to yield the title compound as a pale yellow solid (0.21 g, 72%).

[0659]

1
H NMR (DMSO-d6) δ 8.32 (t, J=5.1, 1H,), 8.04 (d, J=8.4, 1H,), 7.33-7.10 (m, 9H), 6.79 (t, J=7.7, 1H,), 6.41 (d, J=8.1, 1H), 6.22 (d, J=7.3, 1H), 5.71 (s br, 1H), 5.46 (d, J=6.8, 1H), 5.14 (d, J=9.2, 1H), 5.01 (d, J=9.2, 1H), 4.48-4.37 (m, 4H), 4.11 (dd, J=15.0, 4.8, 1H), 3.07 (m, 2H), 2.84-2.67 (m, 2H), 2.32-2.26 (m, 2H), 2.26 (s, 3H), 1.59 (m, 2H), 1.49 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C34H40N4O4SNa (M+Na)+ 623.2662, found 623.2669; Anal. Calcd for C34H40N4O4S: C, 66.97; H, 6.78; N, 9.18. Found: C, 66.97; H, 6.73; N, 9.12.

Specific Urea Synthesis

EXAMPLE B3

3-(2-hydroxy-3-{[1-(3-hydroxy-pyrrolidin-yl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic acid-2-methyl-benzylamide

[0660]

217

[0661] (R)-Pyrrolidin-3-ol (0.21 g, 2.40 mmol) was dissolved in dry CH2Cl2 (15 mL) and cooled to −78° C. under argon with magnetic stirring. To this solution was added Diisopropylethylamine (0.63 mL, 3.63 mmol) followed by Phosgene as a 20% solution in toluene (1.2 mL, 2.40 mmol). The resulting yellow solution was stirred for 20 min at −78-C then allowed to warm to room temperature. The solution was concentrated and re-dissolved in dry CH2Cl2 (5 mL) and THF (5 mL). To this was added Diisopropylethylamine (0.31 mL, 1.81 mmol) followed by 16c. The result was stirred for 16 h at 23° C. then diluted with EtOAc (50 mL). The mixture was washed sequentially with 10% citric acid (1×50 mL), saturated NaHCO3 (1×50 mL), H2O (1×50 mL). The organics were dried over Na2SO4, filtered, and concentrated. The residue was purified by flash column chromatography (5% MeOH in EtOAc) to yield the title compound (0.12 g, 18%) as a white foam.

[0662]

1
H NMR (DMSO-d6) δ 8.38 (t, J=5.7, 1H), 7.34-7.09 (m, 10H), 5.99 (d, J=8.3, 1H), 5.04 (d, J=9.5, 1H), 4.96 (d, J=9.5, 1H), 4.49 (s, 1H), 4.48-4.38 (m, 3H), 4.22-3.83 (m, 4H), 3.29-3.04 (m, 3H), 2.77-2.70 (m, 2H), 2.28 (s, 3H), 1.52 (s, 3H), 1.32 (s, 3H), 1.82-1.69 (m, 2H); HRMS (ESI) m/z calcd for C29H38N4O5SNa (M+Na)+ 577.2455, found 577.2440; Anal. Calcd for C29H38N4O5S.2H2O: C, 58.96; H, 7.17; N, 9.48; S, 5.43. Found: C, 58.90; H, 6.40; N, 9.23; S, 5.24.

[0663] The following examples were prepared by the corresponding specific method outlined above using the requisite P2 fragment.

EXAMPLE B4

3-{2-Hydroxy-4-phenyl-3-[2-(2H-[1,2,4t]triazol-3-ylsufanyl)-ethanoylamino]-butanoyl}5,5-dimethyl-thiazolidine-4-carboxylic acid-2-methyl-benzylamide

[0664]

218

[0665]

1
H NMR (DMSO-d6) δ 14.00 (s br, 1H), 8.54 (s br, 1H), 8.35 (t, J=5.7, 1H), 8.30) (s br, 1H), 7.32-7.06 (m, 10H), 4.98 (d, J=9.2, 1H), 4.92 (d, J=9.2, 1H), 4.50 (s, 1H), 4.43-4.36 (m, 2H), 4.12 (m, 2H), 3.77 (s br, 2H), 2.76-2.58 (m, 2H), 2.26 (s, 3H), 1.50 (s, 3H), 1.32 (s, 3H); HRMS (ESI) m/z calcd for C28H34N6O4S2Na (M+Na)+ 605.1975, found 605.1988; Anal. Calcd for C28H34N6O4S2.0.25H2O: C, 57.27; H, 5.92; N, 14.31; S, 10.92. Found: C, 57.21; H, 5.97; N, 14.10; S, 10.71.

EXAMPLE B5

{(1S,2S)-1-Benzyl-3-[(R)-5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid (R)-2-isopropyl-tetrahydro-thiophen-3-yl Ester

[0666]

219

[0667]

1
H NMR (DMSO-d6) δ 8.38 (s br, 2H), 7.42-7.09 (m, 9H), 5.12 (s, 1H), 4.99 (s, 2H), 4.52-3.80 (m, 5H), 3.19-2.79 (m, 6H), 2.29 (s, 3H), 1.99-1.71 (m, 3H), 1.51 (s, 3H), 1.39 (s, 3H), 0.99 (m, 6H); Anal. Calcd for C32H43N3O5S2: C, 62.61; H, 7.06; N, 6.85. Found: C, 62.45; H, 6.84; N, 7.04.

EXAMPLE B6

2,3-Dihydro-1H-indole-4-carboxylic Acid {(1S,2S)-1-benzyl-3-[(R)-5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-amide

[0668]

220

[0669] Pale yellow solid; IR (neat, cm−1) 3417, 1644, 1529, 1453, 1114; 1H NMR (DMSO-d6) δ 8.35 (t, J=5.1, 1H), 8.06 (d, J=8.6, 1H), 7.34-7.11 (m, 9H), 6.91 (t, J=7.7, 1H), 6.78 (d, J=5.5, 1H), 6.70 (d, J=7.5, 1H), 6.53 (d, J=7.7, 1H), 5.58 (s, 1H), 5.10 (d, J=9.2, 1H), 5.00 (d, J=9.2, 1H), 4.51-4.36(m, 4H), 4.13 (dd, J=15.0, 4.6, 1H), 3.34-3.29 (m, 2H), 2.80-2.00 (m, 4H), 2.25 (s, 3H), 1.50 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C33H38N4O4SNa (M+Na)+ 609.2506, found 609.2485.

EXAMPLE B7

(R)-3-{(2S,3S)-3-[2-(2,6-Dimethylphenoxy)-ethanoylamino]-2-hydroxy-4-phenyl-butanoyl}-5,5-dimethylthiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0670]

221

EXAMPLE B8

1H-Indole-4-carboxylic Acid {(1S,2S)-1-benzyl-3-[(R)-5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-amide

[0671]

222

[0672] White solid; IR (neat, cm−1) 3422, 1642, 1520, 1349, 1114; 1H NMR (DMSO-d6) δ 11.24 (s, 1H), 8.36 (t, J=6.1, 1H), 8.18 (d, J=8.2, 1H), 7.50 (d, J=8.1, 1H), 7.51-7.06 (m, 12H), 6.71 (s, 1H), 5.48 (d, J=6.4, 1H), 5.11 (d, J=9.3, 1H), 5.04 (d, J=9.3, 1H), 4.58-4.49 (m, 3H), 4.39 (dd, J=15.2, 6.6, 1H), 4.14 (dd, J=15.2, 4.9, 1H), 2.86 (m, 2H), 2.25 (s, 3H), 1.51 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C33H36N4O4SNa (M+Na)+ 607.2349, found 607.2350.

EXAMPLE B9

1H-Indazle-4-carboxylic Acid {1-benzyl-3-[5,5-dimethyl-4-(2-methyl-benzyl carbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-amide

[0673]

223

[0674]

1
H NMR (DMSO-d6) δ 13.18 (s, 1H), 8.46 (d, J=8.2, 1H), 8.35 (t, J=5.6, 1H), 8.20 (s, 1H), 7.68-7.06 (m, 12H), 5.53 (d, J=6.6, 1H), 5.13 (d, J=9.1, 1H), 5.06 (d, J=9.1, 1H), 4.61-4.54 (m, 2H), 4.51 (s, 1H), 4.40 (dd, J=14.9, 6.2, 1H), 4.16 (dd, J=14.9, 4.7, 1H), 2.91-2.89 (m, 2H), 2.51 (s, 3H), 1.53 (s, 1), 1.31 (s, 3H); HRMS (ESI) m/z calcd for C32H35N5O4SNa (M+Na)+ 608.2302, found 608.2273; Anal. Calcd for C32H35N5O4S.0.35H2O: C, 64.92; H, 6.08; N, 11.83; S, 5.42. Found: C, 65.15; H, 6.21; N, 11.44; S, 5.13.

EXAMPLE B10

{(1S,2S)-1-Benzyl-3-[(R)-5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid prop-2-ynyl Ester

[0675]

224

[0676] Isolated yield: 83%; 1H-NMR (400 MHz, dmso-d6): δ 8.30 (t, 1H), 7.48 (d, 1H), 7.0-7.3 (m, 10H), 5.35 (d, 1H), 4.96 (q, 2H), 4.48-4.31 (m, 5H), 4.14 (dd, 1H), 3.87 (m, 1H), 3.44 (s, 1H), 2.7 (dd, 1H), 2.61 (t, 1H), 2.26 (s, 3H), 1.48 (s, 3H), 1.35 (s, 3H); IR (KBr in cm−1): 3302, 1711, 1643, 1528, 1237, 1047; MS (APCI, m/z): 524 (M+H): C28H33N3O5S1.0.21H2O Calculated: C, 63.76; H, 6.39; N, 7.97, Observed: C, 64.22; H, 6.35; N, 8.02. HPLC: Rf (min.) 20.177; Purity: 99%.

EXAMPLE B11

{(1S,2S)-1-Benzyl-3-[(R)-5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid Allyl Ester

[0677]

225

[0678] Isolated yield: 83%; 1H-NMR (400 MHz, dmso-d6): δ 8.30 (t, 1H), 7.04-7.35 (m, 10H), 5.7-5.83 (m, 1H), 5.3 (d, 1H), 5.09 (d, 1H), 5.14 (d, 1H), 4.96 (q, 2H), 4.3 (s, 1H), 4.3-4.43 (m, 4H), 4.13 (dd, 1H), 3.87 (m, 1H) 2.74 (dd, 1H), 2.61 (dd, 1H), 2.26 (s, 3H), 1.48 (s, 3H), 1.30 (s, 3H); IR (KBr in cm−1): 3324, 1691, 1645, 1530, 1238, 1041; MS (APCI, m/z): 526 (M+H), 468; C28H35N3O5S1.0.35H2O Calculated: C, 63.22; H, 6.76; N, 7.90. Observed: C, 663.98; H, 6.71; N, 7.99. HPLC: Rf (min.) 20.97; Purity: 98%.

EXAMPLE B12

(R)-3-[(2S,3S)-2-Hydroxy-3-(2-methyl-butyrylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0679]

226

[0680] Isolated yield: 75%; 1H-NMR (400 MHz, dmso-d6): δ 8.37 (q, 1H), 7.71 (d, 1H), 7.04-7.37 (m, 9H), 5.24 (brd, 1H), 5.11 (t, 1H), 5.04 (dd, 1H), 4.5-4.28 (m, 3H), 4.15 (m, 2H), 2.75-2.54 (m, 2H), 2.28 (s, 3H), 2.11 (m, 1H), 1.5 (s, 3H), 1.27 (s, 3H). 1.02-1.24 (m, 2H), 0.93 (d)+0.7 (m)+0.41 (t) 6H; IR (KBr in cm−1): 3311, 2966, 1642, 1530; MS (APCI, m/z): 526 (M+H), 480, 265; C29H39N3O4S1.0.38H2O Calculated: C, 65.41; H, 7.53; N, 7.89. Observed: C, 66.26; H, 7.48; N, 7.99. HPLC: Rf (min.) 20.68; Purity: 100%.

EXAMPLE B13

(R)-3-[(2S,3S)-3-(3-Allyl-ureido)-2-hydroxy-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0681]

227

[0682] Isolated yield: 65%; 1H-NMR (400 MHz, dmso-d6): δ 8.35 (t, 1H), 7.35-7.04 (m, 10H), 6.13 (d, 1H), 5.96 (t, 1H), 5.70 (m, 1H), 5.13-4.87 (m, 5H), 4.5-4.35 (m, 2H), 4.17 (dd, 1H), 4.04 (t, 1H), 3.52 (m, 2H), 2.22 (s, 3H), 1.48 (s, 3H), 1.32 (s, 3H); MS (APCI, m/z): 541 (M+H), 442, 396, 277; HPLC: Rf (min.) 21.05; Purity: >95%.

EXAMPLE B14

{(1S,2S)-1-Benzyl-3-[(R)-5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid but-3-enyl Ester

[0683]

228

[0684] Isolated yield: 81%; 1H-NMR (400 MHz, dmso-d6): δ 8.26 (t, 1H), 7.0-7.27 (m, 10H) 5.7-5.56 (m, 1H), 5.27 (d, 1H), 4.83-5.04 (m, 4H), 4.4 (s, 1H), 4.35 (m, 2H), 4.13 (dd, 1H), 3.65-3.87 (m, 2H), 2.65 (d, 1H), 2.52 (m, 1H), 2.22 (s, 3H), 2.17 (m, 2H), 1.44 (s, 3H), 1.26 (s, 3H); MS (APCI, m/z): 540 (M+H), 468; HPLC: Rf (min.) 21.31; Purity: 96%.

EXAMPLE B15

3-[(S)-3-(Cyclopropanecarbonyl-amino)-2-hydroxy-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0685]

229

[0686] Isolated yield: 78%; 1H-NMR (400 MHz, dmso-d6): δ 8.35 (t, 1H), 8.26 (d, 1H), 7.0-7.26 (m, 10H), 5.174 (d, 1H), 5.0 (d, 1H), 4.87 (d, 1H), 4.44 (s, 1H), 4.3-4.44 (m, 2H), 4.17-4.04 (m, 2H), 2.30-2.70 (m, 2H), 1.52 (m, 1H), 1.44 (s, 3H), 1.30 (s, 3H), 0.52 (m, 2H), 0.44 (m, 2H); MS (APCI, m/z): 510 (M+H), 265; HPLC: Rf (min.) 19.857; Purity: 94%.

EXAMPLE B16

{(S)-1-Benzyl-3-[5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid Isopropyl Ester

[0687]

230

[0688] Isolated yield: 81%; 1H-NMR (400 MHz, dmso-d6): δ 8.26 (t, 1H), 7.0-7.30 (m, 10H), 5.26 (brs, 1H), 4.91 (q, 2H), 4.35-4.13 (m, 2H), 4.13 (dd, 1H), 4.83 (t, 1H), 3.7 (q, 1H), 2.66 (dd, 1H), 2.52 (t, 1H), 2.2 (s, 3H), 1.44 (s, 3H), 1.26 (s, 3H), 0.74 (t, 6H); MS (APCI, m/z): 528 (M+H), 468; HPLC: Rf (min.) 21.127; Purity: 98%.

EXAMPLE B17

3-[(S)-2-Hydroxy-3-(3-isopropyl-ureido)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0689]

231

[0690] Isolated yield: 81%; 1H-NMR (400 MHz, dmso-d6): δ 8.35 (t, 1H), 7.0-7.32 (m, 10H), 5.87 (d, 1H), 5.7 (d, 1H), 5.17 (d, 1H), 5.03 (d, 1H), 4.91 (d, 1H), 4.48-4.3 (m, 2H), 4.44 (s, 1H), 4.17 (dd, 1H), 4.0 (m, 1H), 3.52 (m, 1H), 2.65 (dd, 1H), 2.22 (s, 3H), 1.48 (s, 3H), 1.35 (s, 3H), 0.91 (d, 3H), 0.83 (d, 3H); MS (APCI, m/z): 527 (M+H), 442, 396, 263; HPLC: Rf (min.) 19.94; Purity: 95%.

EXAMPLE B18

(R)-3-((2S,3S)-2-Hydroxy-3-pent-4-ynoylamino-4-phenyl-butyryl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0691]

232

[0692] Isolated yield: 79%; 1H-NMR (400 MHz, dmso-d6): δ 8.35 (t, 1H), 8.08 (d, 1H), 7.35-7.0 (m, 10H), 5.26 (d, 1H), 5.04 (d, 1H), 5.87 (d, 1H), 4.48 (s, 1H), 4.38 (m, 2H), 4.15 (m, 2H), 2.74-2.52 (m, 2H), 2.22 (s, 3H), 2.17 (m, 4H), 1.48 (s, 3H), 1.30 (s, 3H); IR (KBr in cm−1): 3294, 1642, 1530, 744; MS (APCI, m/z): 522 (M+H), 476, 265; C30H36N4O4S1.2.44H2O Calculated: C, 60.80; H, 6.95; N, 9.45. Observed: C, 65.67; H, 6.61; N, 10.21. HPLC: Rf (min.) 19.787; Purity: 100%.

EXAMPLE B19

(R)-3-[(2S,3S)-2-Hydroxy-4-phenyl-3-(3,3,3-trifluoropropionylamino)-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0693]

233

[0694] Isolated yield: 72%; 1H-NMR (400 MHz, dmso-d6): δ 8.48 (d, 1H), 8.38 (t, 1H), 7.35-7.04 (m, 10H), 5.35 (d, 1H), 5.0 (d, 1H), 4.92 (d, 1H), 4.48 (s, 1H), 4.38 (m, 2H), 4.17 (m, 2H), 3.14 (m, 2H), 2.7 (d, 1H), 2.6 (t, 1H), 2.26 (s, 3H), 1.48 (s, 3H), 1.35 (s, 3H); IR (KBr in cm−1): 3305, 1649, 1534, 1239, 1110, 743; MS (APCI, m/z): 552 (M+H), 431, 265; C27H32N3O4S1F3.0.41H2O Calculated: C, 58.01; H, 5.92; N, 7.52. Observed: C, 58.79; H, 5.85; N, 7.62. HPLC: Rf (min.) 20.319; Purity: 100%.

EXAMPLE B20

(R)-3-((2S,3S)-3-Butyrylamino-2-hydroxy-4-phenyl-butyryl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0695]

234

[0696] Isolated yield: 72%; 1H-NMR (400 MHz, dmso-d6): δ 8.35 (t, 1H), 7.96 (d, 1H), 7.35-7.04 (m, 10H), 5.22 (d, 1H), 5.09 (d, 1H), 4.91 (d, 1H), 4.48 (s, 1H), 4.38 (m, 2H), 4.17 (m, 2H), 2.67 (d, 1H), 2.56 (t, 1H), 2.26 (s, 3H), 1.91 (t, 2H), 1.48 (s, 3H), 1.30 (s+m, 5H), 0.65 (t, 3H); IR (KBr in cm−1): 3308, 2967, 1641, 1534, 743; MS (APCI, m/z): 512 (M+H), 466, 265; C28H35N3O4S1.0.48H2O Calculated: C, 65.16; H, 7.03; N, 7.71. Observed: C, 65.16; H, 7.09; N, 8.44. HPLC: Rf (min.) 20.070; Purity: 95%.

EXAMPLE B21

2,3-Dihydro-1H-indole-4-carboxylic Acid [(1S,2S)-3-((R)-4-allylcarbamoyl-5,5-dimethyl-thiazolidin-3-yl)-1-benzyl-2-hydroxy-3-oxo-propyl]-amide

[0697]

235

[0698] Beige solid; 1H NMR (DMSO-d6) δ 8.09 (t, J=5.7, 1H), 8.00 (d, J=8.6, 1H), 7.70 (d, J=7.7, 1H), 7.34-7.11 (m, 6H), 6.91 (t, J=7.9, 1H), 6.68 (d, J=8.1, 1H), 5.80-5.71 (m, 1H), 5.58 (s, 1H), 5.44 (d, J=7.0, 1H), 5.23-5.01 (m, 4H), 4.47-4.39 (m, 4H), 3.73-3.61 (m, 2H), 2.99-2.81 (m, 4H), 1.50 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C28H34N4O4SNa (M+Na)+ 545.219, found 545.2205.

EXAMPLE B22

[(1S,2S)-3-((R)-4-Allylcarbamoyl-5,5-dimethyl-thiazolidin-3-yl)-1-benzyl-2-hydroxy-3-oxo-propyl]-carbamic Acid (S)-(tetrahydro-furan-3-yl) Ester

[0699]

236

[0700] White solid; 1H NMR (DMSO-d6) δ 8.06 (t, J=5.9, 1H), 7.27-7.12 (m, 6), 5.76 (m, 1H), 5.39 (d, J=7.1, 1H), 5.19 (dd, J=17.2, 1.7, 1H), 5.03-4.90 (m, 4H), 4.39-4.35 (m, 2H), 3.88 (m, 1H), 3.76-3.58 (m, 5H), 3.42 (d, J=10.4, 1H), 2.75-2.55 (m, 2H), 2.03 (m, 1H), 1.80 (m, 1H), 1.49 (s, 3H), 1.34 (s, 3H); HRMS (ESI) m/z calcd for C24H33N3O6SNa (M+Na)+ 514.1982, found 514.1967.

EXAMPLE B23

(R)-3-{(2S,3S)-3-[2-(2,6-Dimethyl-phenoxy)-ethanoylamino]-2-hydroxy-4-phenyl-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid Allylamide

[0701]

237

[0702] White solid; IR (neat, cm−1) 3418, 1651, 1532, 1454, 1372, 1264, 1195; 1H NMR (DMSO-d6) δ 8.15 (t, J=5.7, 1H), 8.10 (d, J=8.8, 1H), 7.32-7.13 (m, 5H), 7.00-6.89 (m, 3H), 5.83-5.71 (m, 1H), 5.48 (d, J=6.8, 1H), 5.21 (dd, J=17.2, 1.8, 1H), 5.03-4.91 (m, 3H), 4.49-4.36 (m, 3H), 4.16 (d, J=14.1, 1H), 3.98 (d, J=14.1, 1H), 3.72 (m, 2H), 2.79-2.76 (m, 2H), 2.13 (s, 6H), 1.50 (s, 3H), 1.36 (s, 3H); HRMS (ESI) m/z calcd for C29H37N3O5SNa (M+Na)+ 562.2346, found 562.2324.

EXAMPLE B24

1-H-indazole-4-carboxylic Acid [3-(4-allylcarbamoyl-5,5-dimethyl-thiazolidin-3-yl)-1-benzyl-2-hydroxy-3-oxo-propyl]-amide

[0703]

238

[0704]

1
H NMR (DMSO-d6) δ 13.18 (s, 1H), 8.42 (d, J=8.2, 1H), 8.19 (s, 1H), 8.10 (t, J=5.7, 1H), 7.68-7.11 (m, 8H), 5.81-5.72 (m, 1H), 5.52 (d, J=6.8, 1H), 5.24-4.83 (m, 4H), 4.57 (m, 2H), 4.42 (s, 1H), 3.74-3.66 (m, 2H), 2.90 (m, 2H), 1.53 (s, 3H), 1.37 (s, 3H); Anal. Calcd for C27H31N5O4S.0.25H2O: C, 61.63; H, 6.04; N, 13.31; S, 6.09. Found: C, 61.63; H, 6.09; N, 12.95; S, 5.95.

EXAMPLE B25

(R)-3-{(2S,3S)-2-Hydroxy-4-phenyl-3-[2-(1H-[1,2,4]triazol-3-ylsulfanyl)-ethanoylamino]-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid Allylamide

[0705]

239

EXAMPLE B26

{(1S,2S)-1-Benzyl-3-[(R)-4-(cyclopropylmethyl-carbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid (S)-(tetrahydro-furan-3-yl) Ester

[0706]

240

[0707] White solid; 1H NMR (DMSO-d6) δ 7.99 (t, J=5.7, 1H), 7.28-7.07 (m, 6H), 5.32 (d, J=7.3, 1H), 4.96-4.92 (m, 3H), 4.38 (s, 1H), 3.90 (m, 1H), 3.76-3.54 (m, 4H), 3.41 (d, J=10.4, 1H), 3.04-2.92 (m, 2H), 2.73-2.54 (m, 2H), 2.03 (m, 1H), 1.83 (m, 1H), 1.49 (s, 3H), 1.36 (s, 3H), 0.88 (m, 1H), 0.35 (m, 2H), 0.15 (m, 2H); HRMS (ESI) m/z calcd for C25H35N3O6SNa (M+Na)+ 528.2139, found 528.2121.

EXAMPLE B27

(R)-3-{(2S,3S)-3-[2-(2,6-Dimethyl-phenoxy)-ethanoylamino]-2-hydroxy-4-phenyl-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid cyclopropylmethyl-amide

[0708]

241

[0709] White solid; IR (neat, cm−) 3413, 1648, 1531, 1443, 1390, 1196; 1H NMR (DMSO-d6) δ 8.12 (d, J=9.0, 1H), 8.06 (t, J=5.7, 1H), 7.33-7.13 (m, 5H), 7.01-6.89 (m, 3H), 5.44 (d, J=6.8, 1H), 4.97 (d, J=9.0, 1H), 4.91 (d, J=9.0, 1H), 4.47-4.36 (m, 2H), 4.41 (s, 1H), 4.16 (d, J=14.2, 1H), 3.98 (d, J=14.2, 1H), 3.10-2.76 (m, 4H), 2.13 (s, 6H), 1.51 (s, 3H), 1.38 (s, 3H), 0.88 (m, 1H), 0.36 (m, 2H), 0.15 (m, 2H); HRMS (ESI) m/z calcd for C30H39N3O5SNa (M+Na)+ 576.2503, found 576.2503.

EXAMPLE 28

2,3-Dihydro-1H-indole-4-carboxylic Acid {(1S,2S)-1-benzyl-3-[(R)-4-(cyclopropylmethyl-carbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-amide

[0710]

242

[0711] Off white solid; 1H NMR (DMSO-d6) δ 8.03-8.01 (m, 2H), 7.35-7.11 (m, 5H), 6.91 (t, J=7.7, 1H), 6.69 (d, J=7.9, 1H), 6.52 (d, J=7.7, 1H), 5.58 (s br, 1H), 5.39 (d, J=6.8, 1H), 5.06 (d, J=9.2, 1H), 4.99 (d, J=9.2, 1H), 4.48-4.39 (m, 4H), 2.98-2.79 (m, 6H), 1.51 (s, 3H), 1.37 (s, 3H), 0.87 (m, 1H), 0.35 (m, 2H), 0.14 (m, 2H); HRMS (ESI) m/z calcd for C29H36N4O4SNa (M+Na)+ 559.2349, found 559.2353.

EXAMPLE B29

2,3-Dihydro-1H-indole-4-carboxylic Acid {(1S,2S)-1-benzyl-3-[(R)-4-((S)-chroman-4-ylcarbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-amide

[0712]

243

[0713] Beige solid; 1H NMR (DMSO-d6) δ 8.52 (d, J=8.1, 1H), 8.21 (d, J=8.4, 1H), 7.54-6.72 (m, 13H), 5.40 (d, J=5.9, 1H), 5.20-4.90 (m, 3H), 4.70-4.12 (m, 3H), 3.10-2.80 (m, 4H), 2.20-1.90 (m, 6H), 1.51 (s, 3H), 1.49 (s, 3H); HRMS (ESI) m/z calcd for C34H38N4O5SNa (M+Na)+ 685.2303, found 685.2319; Anal. Calcd for C34H38N4O5S.0.5H2O: C, 65.47; H, 6.30; N, 8.98. Found: C, 65.34; H, 6.02; N, 8.75.

EXAMPLE B30

(R)-3-{(2S,3S)-3-[2-(2,6-Dimethyl-phenoxy)-ethanoylamino]-2-hydroxy-4-phenyl-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-chroman-4-ylamide

[0714]

244

[0715] White solid: mp=105-107° C.; 1H NMR (DMSO-d6) δ 8.49 (d, J=7.7, 1H), 8.14 (d, J=8.6, 1H), 7.40-6.65 (m, 12H), 5.44 (d, J=7.3, 1H), 4.96 (d, J=8.6, 1H), 4.94 (d, J=8.6, 1H), 4.44-3.94 (m, 8H), 2.82-2.70 (m, 2H), 2.15 (s, 6H), 2.10-1.90 (m, 2H), 1.49 (s, 3H), 1.45 (s, 3H); HRMS (ESI) m/z calcd for C35H41N3O6SNa (M+Na)+ 654.2608, found 654.2622; Anal. Calcd for C35H41N3O6S: C, 66.54; H, 6.54; N, 6.65. Found: C, 66.54; H, 6.68; N, 6.69

EXAMPLE B31

(R)-3-{(2S,3S)-2-Hydroxy-4-phenyl-3-[2-(1H-[1,2,4]triazol-3-ylsulfanyl)-ethanoylamino]-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-chroman-4-ylamide

[0716]

245

[0717]

1
H NMR (DMSO-d6) δ 8.47 (d, J=8.2, 1H), 8.37 (d, J=8.6, 1H), 8.23 (s br, 1H), 7.20-7.08 (m, 7H), 6.85-6.74 (m, 2H), 5.26 (d, J=6.6, 1H), 4.98-4.89 (m, 3H), 4.41 (s, 1H), 4.30-4.20 (m, 4H), 3.75 (dd, J=22.2, 14.5, 2H), 2.75-2.50 (m, 2H), 2.20-1.90 (m, 2H), 1.48 (s, 3H), 1.44 (s, 3H); HRMS (ESI) m/z calcd for C29H34N6O5S2Na (M+Na)+ 633.1924, found 633.1930.

EXAMPLE B32

((1S,2S)-1-Benzyl-3-{(R)-5,5-dimethyl-4-[(S)-(1,2,3,4-tetrahydro-naphthalen-1-yl)carbamoyl]-thiazolidin-3-yl}-2-hydroxy-3-oxo-propyl)-carbamic Acid 2,6-dimethyl-benzyl Ester

[0718]

246

[0719] White solid: mp=88-90° C.; 1H NMR (DMSO-d6) δ 8.30 (d, J=8.9, 1H), 8.15 (d, J=9.3, 1H), 7.35-6.85 (m, 12H), 5.45 (d, J=6.0, 1H), 5.20-4.90 (m, 2H), 4.45-390 (m, 6H), 2.80-2.62 (m, 2H), 2.14 (s, 6H), 1.90-1.60 (m, 6H), 1.49 (s, 3H), 1.45 (s, 3H); HRMS (ESI) m/z calcd for C36H43N3O5SNa (M+Na)+ 652.2816, found 652.2836; Anal. Calcd for C36H43N3O5S: C, 68.65; H, 6.88; N, 6.67. Found: C, 68.45; H, 6.98; N, 6.58.

EXAMPLE B33

((1S,2S)-1-Benzyl-3-((R)-5,5-dimethyl-4-[(S)-(1,2,3,4-tetrahydro-acid (S)-(tetrahydro-furan-3-yl) Ester

[0720]

247

[0721] White solid: mp=103-105° C.; 1H NMR (DMSO-d6) δ 8.26 (d, J=7.9, 1H), 7.30-7.08 (m, 10H), 5.50 (d, J=7.9, 1H), 5.00-4.90 (m, 3H), 4.42-4.38 (m, 3H), 4.00-3.30 (m, 5H), 3.00-2.40 (m, 4H), 1.90-1.60 (m, 4H), 1.47 (s, 3H), 1.43 (s, 3H), 1.40-1.38 (m, 2H); HRMS (ESI) m/z calcd for C31H39N3O6SNa (M+Na)+ 604.2452, found 604.2430; Anal. Calcd for C31H39N3O6S.0.25H2O: C, 63.51; H, 6.79; N, 7.17. Found: C, 63.40; H, 6.73; N, 7.08.

EXAMPLE B34

2,3-Dihydro-1H-indole-4-carboxylic Acid [(1S,2S)-1-benzyl-3-((R)-5,5-dimethyl-4-prop-2-ynylcarbamoyl-thiazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-amide

[0722]

248

[0723] Orange solid; 1H NMR (DMSO-d6) δ 8.41 (t, J=5.0, 1H), 8.01 (d, J=8.3, 1H), 7.34-7.11 (m, 5H), 6.91 (t, J=7.7, 1H), 6.68 (d, J=7.5, 1H), 6.52 (d, J=7.9, 1H), 5.58 (s br, 1H), 5.45 (d, J=6.8, 1H), 5.06 (d, J=9.3, 1H), 4.99 (d, J=9.5, 1H), 4.48-4.37 (m, 4H), 3.84 (m, 2H), 3.09 (m, 1H), 2.98-2.81 (m, 4H), 1.50 (s, 3H), 1.35 (s, 3H); HRMS (ESI) m/z calcd for C28H32N4O4SNa (M+Na)+ 543.2036, found 543.2039.

EXAMPLE B35

1-H-indazole-4-carboxylic Acid [1-benzyl-3-(5,5-dimethyl-4-prop-2-ynylcarbamoyl-thiazolidin-3-yl)-2-hydroxy-3-oxo-propyl-amide

[0724]

249

[0725]

1
H NMR (DMSO-d6) δ 13.18 (s, 1H), 8.42 (m, 2H), 8.19 (s, 1H), 7.68-7.12 (m, 8H), 5.54 (d, J=5.6, 1H), 5.10 (d, J=9.3, 1H), 5.08 (d, J=9.3, 1H), 4.54 (m, 2H), 4.41 (s, 1H), 3.87 (m, 2H), 3.03 (t, J=2.5, 1H), 2.89 (m, 2H), 1.53 (s, 3H), 1.38 (s, 3H); HRMS (ESI) m/z calcd for C27H29N5O4SNa (M+Na)+ 542.1832, found 542.1855; Anal. Calcd for C27H29N5O4S.0.25H2O: C, 61.87; H, 5.67; N, 13.36; S, 6.12. Found: C, 61.85; H, 5.64; N, 13.19; S, 6.08.

EXAMPLE B36

(R)-3-{(2S,3S)-3-[2-(2,6-Dimethyl-phenoxy)-ethanoylamino]-2-hydroxy-4-phenyl-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid prop-2-ynylamide

[0726]

250

[0727] White solid; IR (neat, cm−1) 3418, 1658, 1530, 1378, 1196; 1H NMR (DMSO-d6) δ 8.46 (t, J=5.1, 1H), 8.10 (d, J=9.0, 1H), 7.33-7.14 (m, 5H), 7.01-6.89 (m, 3H), 5.49 (d, J=6.8, 1H), 4.97 (d, J=9.2, 1H), 4.92 (d, J=9.0, 1H), 4.48-4.35 (m, 2H), 4.40 (s, 1H), 4.15 (d, J=14.3, 1H), 3.99 (d, J=14.1, 1H), 3.93-3.86 (m, 2H), 3.10 (s, 1H), 2.77 (m, 2H), 1.50 (s, 3H), 1.37 (s, 3H), 2.13 (s, 6H); HRMS (ESI) m/z calcd for C29H35N3O5SNa (M+Na)+ 560.2190, found 560.2168.

EXAMPLE B37

1-H-indazole-4-carboxylic Acid (1-benzyl-3-4 [(furan-2-ylmethyl)-carbamoyl]-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl)-amide

[0728]

251

[0729]

1
H NMR (DMSO-d6) δ 13.18 (s, 1H), 8.44 (m, 2H), 8.19 (s, 1H), 7.68-7.12 (m, 9H), 6.34 (m, 1H), 6.26 (m, 1H), 5.54 (d, J=6.6, 1H), 5.10 (d, J=9.2, 1H), 5.06 (d, J=9.2, 1H), 4.55 (m, 2H), 4.44 (s, 1H), 4.29 (m, 2H), 2.90 (m, 2H), 1.51 (s, 3H), 1.30 (s, 3H); HRMS (ESI) m/z calcd for C29H31N5O5SNa (M+Na)+ 584.1938, found 584.1922; Anal. Calcd for C29H31N5O5S.0.5H2O: C, 61.03; H, 5.65; N, 12.27; S, 5.62. Found: C, 61.14; H, 5.60; N, 12.17; S, 5.60.

EXAMPLE B38

(R)-3-{(2S,3S)-3-[2-(2,6-Dimethyl-phenoxy)-ethanoylamino]-2-hydroxy-4-phenyl-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (furan-2-ylmethyl)-amide

[0730]

252

[0731] White solid; IR (neat, cm−1) 3409, 1657, 1530, 1452, 1371, 1195; 1H NMR (DMSO-d6) δ 8.47 (t, J=5.7, 1H), 8.12 (d, J=8.8, 1H), 7.52 (s, 1H), 7.32-7.14 (m, 5H), 7.01-6.89 (m, 3H), 6.33 (m, 1H), 6.26 (m, 1H), 5.50 (d, J=7.0, 1H), 4.97 (d, J=9.0, 1H), 4.92 (d, J=9.0, 1H), 4.46-4.27 (m, 5H), 4.15 (d, J=14.3, 1H), 4.00 (d, J=14.3, 1H), 2.79 (m, 2H), 2.14 (s, 6H), 1.48 (s, 3H), 1.31 (s, 3H); HRMS (ESI) m/z calcd for C31H37N3O6SNa (M+Na)+ 602.2295, found 602.2310.

EXAMPLE B39

2,3-Dihydro-1H-indole-4-carboxylic Acid ((1S,2S)-1-benzyl-3-{(R)-4-[(furan-2-ylmethyl)-carbamoyl]-5,5-dimethyl-thiazolidin-3-yl}-2-hydroxy-3-oxo-propyl)-amide

[0732]

253

[0733] Pale pink solid; 1H NMR (DMSO-d6) δ 8.42 (t, J=5.3, 1H), 8.02 (d, J=8.2, 1H), 7.53 (s, 1H), 7.34-7.11 (m, 6H), 6.91 (t, J=7.7, 1H), 6.69 (d, J=7.7, 1H), 6.52 (d, J=7.7, 1H), 6.34 (m, 1H), 6.25 (m, 1H), 5.58 (s br, 1H), 5.46 (d, J=6.6, 1H), 5.06 (d, J=9.2, 1H), 4.99 (d, J=9.2, 1H), 4.48-4.18 (m, 5H), 4.40 (s, 1H), 3.00-2.79 (m, 4H), 1.48 (s, 3H), 1.30 (s, 3H).

EXAMPLE B40

(R)-3-{(2S,3S)-2-Hydroxy-4-phenyl-3-[((S)-1-tetrahydro-furan-2-yl-methanoyl)-amino]-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (furan-2-ylmethyl)-amide

[0734]

254

[0735] Off white solid; 1H NMR (DMSO-d6) δ 8.44 (t, J=5.3, 1H), 7.57 (d, J=9.0, 1H), 7.53 (s, 1H), 7.23-7.15 (m, 5H), 6.34 (m, 1H), 6.26 (m, 1H), 5.45 (d, J=6.8, 1H), 4.94 (s, 2H), 4.39 (s, 2H), 4.28 (m, 3H), 4.10 (m, 1H), 3.79-3.64 (m, 2H), 2.79-2.64 (m, 2H), 1.98-1.87 (m, 2H), 1.65-1.33 (m, 2H), 1.47 (s, 3H), 1.30 (s, 3H); HRMS (ESI) m/z calcd for C26H33N3O6SNa (M+Na)+ 538.1982, found 538.1997.

EXAMPLE B41

2,3-Dihydro-1H-indole-4-carboxylic Acid {(1S,2S)-1-benzyl-3-[(R)-4-((S)-cyclohex-2-enylcarbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-amide

[0736]

255

[0737]

1
H NMR (DMSO-d6) δ 8.01 (d, J=8.2, 1H), 7.94 (d, J=7.7, 1H), 7.36-7.06 (m, 5H), 6.90 (t, J=7.6, 1H), 6.69 (d, J=7.6, 1H), 6.52 (d, J=7.6, 1H), 5.80-5.68 (m, 1H), 5.35 (d, J=6.7, 1H), 5.07 (d, J=9.2, 1H), 4.98 (d, J=9.2, 1H), 4.49-4.32 (m, 3H), 4.32-4.20 (m, 1H), 3.00-2.71 (m, 6H), 2.00-1.60 (m, 6H), 1.49 (s, 3H), 1.37 (s, 3H); HRMS (ESI) m/z calcd for C31H38N4O4SNa (M+Na)+ 585.2506, found 585.2500; Anal. Calcd for C31H38N4O4S.1H2O: C, 64.11; H, 6.94; N, 9.65. Found: C, 64.38; H, 6.72; N, 9.54.

EXAMPLE B42

2,3-Dihydro-1H-indole-4-carboxylic Acid {(1S,2S)-1-benzyl-2-hydroxy-3-[(R)-4-((S)-indan-1-ylcarbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-3-oxo-propyl-amide

[0738]

256

[0739]

1
H NMR (DMSO-d6) δ 8.32 (d, J=8.1, 1H), 8.06 (d, J=8.6, 1H), 7.33-7.11 (m, 9H), 6.91 (t, J=7.6, 1H), 6.71 (d, J=7.6, 1H), 6.53 (d, J=7.6, 1H), 5.36-5.25 (m, 2H), 5.09 (d, J=9.2, 1H), 5.01 (d, J=9.2, 1H), 4.50 (d, J=3.6, 1H), 4.44 (s, 1H), 4.42-4.32 (m, 1H), 2.97-2.71 (m, 6H), 2.39-2.34 (m, 2H), 1.87-1.80 (m, 2H), 1.50 (s, 3H), 1.44 (s, 3H); HRMS (ESI) m/z calcd for C34H38N4O4SNa (M+Na)+ 621.2506, found 621.2519; Anal. Calcd for C34H38N4O4S.0.25H2O: C, 67.69; H, 6.43; N, 9.29. Found: C, 67.73; H, 6.26; N, 8.98.

EXAMPLE B43

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2,4-dimethyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-indan-1-ylamide

[0740]

257

[0741]

1
H NMR (DMSO-d6) δ 8.33 (d, J=7.7, 1H), 8.24 (s, 1H), 8.14 (d, J=8.4, 1H), 7.32-7.12 (m, 9H), 6.86 (d, J=7.7, 1H), 6.53 (d, J=7.7, 1H), 5.38-5.26 (m, 2H), 5.14 (d, J=9.2, 1H), 5.03 (d, J=9.2, 1H), 4.60-4.30 (m, 4H), 2.95-2.64 (m, 3H), 2.42-2.30 (m, 1H), 1.90-1.80 (m, 1H), 2.12 (s, 3H), 1.85 (s, 3H), 1.49 (s, 3H), 1.44 (s, 3H); HRMS (ESI) m/z calcd for C34H39N3O5SNa (M+Na)+ 624.2503, found 624.2509; Anal. Calcd for C34H39N3O5S: C, 67.86; H, 6.53; N, 6.98. Found: C, 67.77; H, 6.50; N, 6.79.

EXAMPLE B44

2,3-Dihydro-1H-indole-4-carboxylic Acid [(1S,2S)-1-benzyl-3-((R)-5,5-dimethyl-4-1[(R)-1-(tetrahydro-furan-2-yl)methyl]-carbamoyl]-thiazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-amide

[0742]

258

[0743] White solid; IR (neat, cm) 3401, 2978, 2861, 1643, 1531, 1455, 1372, 1279, 1073; 1H NMR (DMSO-d6) δ 8.04 (m, 2H), 7.35-7.11 (m, 6H), 6.90 (t, J=7.7, 1H), 6.68 (d, J=7.7, 1H), 6.52 (d, J=7.7, 1H), 5.58 (s br, 1H), 5.39 (d, J=6.8, 1H), 5.06 (d, J=9.2, 1H), 4.97 (d, J=9.3, 1H), 4.49-4.36 (m, 3H), 3.83-3.56 (m, 4H), 3.15 (m, 2H), 2.99-2.78 (m, 4H), 1.78 (m, 4H), 1.50 (s, 3H), 1.36 (s, 3H); HRMS (ESI) m/z calcd for C30H38N4O5SNa (M+Na)+ 589.2455, found 589.2440.

EXAMPLE B45

2,3-Dihydro-1H-indole-4-carboxylic Acid [(1S,2S)-1-benzyl-3-((R)-5,5-dimethyl-4-propylcarbamoyl-thiazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-amide

[0744]

259

[0745] Pink solid; 1H NMR (DMSO-d6) δ 8.01 (d, J=8.2, 1H), 7.89 (t, J=5.3, 1H), 7.35-7.10 (m, 5H), 6.90 (t, J=7.8, 1H), 6.68 (d, J=7.8, 1H), 6.52 (d, J=7.8, 1H), 5.57 (s, 1H), 5.39 (d, J=6.9, 1H), 5.05 (d, J=9.2, 1H), 4.98 (d, J=9.2, 1H), 4.49-4.40 (m, 2H), 4.35 (s, 1H), 3.04-2.78 (m, 8H), 1.49 (s, 3H), 1.34 (s, 3H), 1.43-1.30 (m, 2H), 0.82 (t, J=7.5, 3H); HRMS (ESI) m/z calcd for C28H36N4O4SNa (M+Na)+ 547.2349, found 547.2323; Anal. Calcd for C28H36N4O54S.0.25H2O: C, 63.55; H, 6.95; N, 10.59. Found: C, 63.33; H, 6.60; N, 10.46.

EXAMPLE B46

3-[(2S,3S)-3-[3-(2-Chloro-benzyl)-ureido]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-chloro-benzylamide

[0746]

260

[0747] 1H-NMR (400 MHz, dmso-d6): 7.00-7.40 (m, 13H), 4.00-4.80 (m, 9H), 2.60 (m, 2H), 1.50, 1.40 (s, 3H), 1.26, 1.22 (s, 3H); MS (APCI, m/z): 628, 630; C31H34Cl2N4O4S Calculated: C, 58.14; H, 5.44; N, 8.90, Observed: C, 58.54; H, 5.41; N, 8.71.

EXAMPLE B47

{(1S,2S)-1-Benzyl-3-[(R)-4-(2-chloro-benzylcarbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid Allyl Ester

[0748]

261

[0749] Isolated yield: 68%; 1H-NMR (400 MHz, dmso-d6): 7.00-7.40 (m, 9H), 6.60 (m, 1H), 5.80 (m, 1H), 5.32 (m, 1H), 5.19 (m, 1H), 4.00-5.00 (m, 9H), 2.75 (m, 2H), 1.56, 1.51 (s, 3H), 1.36, 1.33 (s, 3H);

[0750] MS (APCI, m/z): 548 (M+H); C27H32ClN3O5S. 0.89H2O Calculated: C, 57.69; H, 6.06; N, 7.22. Observed: C, 57.30; H, 5.70; N, 7.22.

EXAMPLE B48

{1-Benzyl-3-[4-(2-chloro-benzylcarbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid prop-2-ynyl Ester

[0751]

262

[0752] Isolated yield: 45%; 1H-NMR (400 MHz, dmso-d 6): 6.88-7.62 (m, 9H), 4.20-5.00 (m, 9H), 2.70-2.90 (m, 2H), 2.42 (t, J=2.5 Hz, 1H), 1.56, 1.50 (s, 3H), 1.37, 1.32 (s, 3H); MS (APCI, m/z): 545 (M+H); C27H30ClN3O5S.0.65H2O Calculated: C, 58.35; H, 5.68; N, 7.56. Observed: C, 57.96; H, 5.48; N, 7.37.

EXAMPLE B49

3-{(2S,3S)-3-[3-(2,6-Difluoro-benzyl)-ureido]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2,6-difluoro-benzylamidea)

[0753]

263

[0754] Isolated yield: 42%; 1H-NMR (400 MHz, dmso-d6): 6.60-7.40 (m, 11H), 4.00-4.80 (m, 9H), 2.60 (m, 2H), 1.50, 1.37 (s, 3H), 1.30, 1.13 (s, 3H); MS (APCI, m/z): 633; C31H32F4N4O4S Calculated: C, 58.85; H, 5.10; N, 8.86. Observed: C, 58.54; H, 5.00; N, 8.71.

EXAMPLE B50

{(1S,2S)-1-Benzyl-3-[(R)-4-(2,6-difluoro-benzylcarbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid Allyl Ester

[0755]

264

[0756] Isolated yield: 71%; 1H-NMR (400 MHz, dmso-d6): 6.60-7.40 (m, 8H), 5.80 (m, 1H), 5.05-5.35 (m, 2H), 4.00-5.00 (m, 9H), 2.75 (m, 2H), 1.56, 1.52 (s, 3H), 1.37, 1.35 (s, 3H); MS (APCI, m/z): 548 (M+H); C27H32ClN3O5S. 0.13H2O Calculated: C, 58.97; H, 5.73; N, 7.64. Observed: C, 58.58; H, 5.61; N, 7.53.

EXAMPLE B51

{1-Benzyl-3-[4-(2,6-difluoro-benzylcarbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid prop-2-ynyl

[0757]

265

[0758] Isolated yield: 73%; 1H-NMR (400 MHz, dmso-d6): 6.60-7.40 (m, 8H), 4.20-5.00 (m, 9H), 2.70-2.90 (m, 2H), 2.42 (m, 1H), 1.56, 1.50 (s, 3H), 1.38, 1.34 (s, 3H); MS (APCI, m/z): 546 (M+H); C27H30ClN3O5S Calculated: C, 59.44; H, 5.36; N, 7.70. Observed: C, 59.33; H, 5.39; N, 7.56.

EXAMPLE B52

3-{(2S,3S)-2-Hydroxy-4-phenyl-3-[3-(2-trifluoromethyl-benzyl)-ureido]-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-trifluoromethyl-benzylamide

[0759]

266

[0760] Isolated yield: 82%; 1H-NMR (400 MHz, dmso-d6): 7.00-7.57 (m, 13H), 4.00-4.80 (m, 9H), 2.60 (m, 2H), 1.46, 1.40 (s, 3H), 1.25, 1.22 (s, 3H); MS (APCI, m/z): 697 (M+H); C33H34F6N4O4S Calculated: C, 56.89; H, 4.92; N, 8.04, Observed: C, 56.33; H, 4.78; N, 7.94.

EXAMPLE B53

{(1S,2S)-1-Benzyl-3-[5,5-dimethyl-4-(2-trifluoromethyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid Allyl Ester

[0761]

267

[0762] Isolated yield: 80%; 1H-NMR (400 MHz, dmso-d6): 7.00-7.70 (m, 9H), 5.80 (m, 1H), 5.20 (m, 2H), 4.00-5.00 (m, 9H), 2.75 (m, 2H), 1.56, 1.50 (s, 3H), 1.40, 1.29 (s, 3H); MS (APCI, m/z): 580 (M+H); C28H32F3N3O5S. 0.56H2O Calculated: C, 57.70; H, 5.60; N, 7.21. Observed: C, 57.31; H, 5.31; N, 6.83.

EXAMPLE B54

{1-Benzyl-3-15,5-dimethyl-4-(2-trifluoromethyl-benzylcarbamoyl)-thiazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid prop-2-ynyl Ester

[0763]

268

[0764] Isolated yield: 61%; 1H-NMR (400 MHz, dmso-d6): 6.90-7.60 (m, 9H), 4.20-5.00 (m, 9H), 2.60-2.80 (m, 2H), 2.42 (m, 1H), 1.55, 1.48 (s, 3H), 1.40, 1.28 (s, 3H); MS (APCI, m/z): 578 (M+H); C28H30F3N3O5S Calculated: C, 58.17; H, 5.24; N, 7.27. Observed: C, 57.78; H, 5.25; N, 6.94.

EXAMPLE B55

3-{(2S,3S)-3-[3-(3-Fluoro-phenyl)-ureido]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0765]

269

[0766] Isolated yield: 40%. 1H NMR (400 MHz, DMSO-d6): δ 8.73 (s, 1H), 8.39 (t, 1H), 7.36-7.10 (m, 1H), 6.91 (d, 1H), 6.65 (t, 1H), 6.45 (d, 1H), 5.33 (br s, 1H), 4.98 (s, 2H), 4.49 (s, 2H), 4.38 (dd, 1H), 4.22-4.12 (m, 2H), 2.58 (d, 2H), 2.55 (m, 1H), 2.24 (s, 3H), 1.49 (s, 3H), 1.35 (s, 3H); MS-APCI (m/z+): 315, 579 (M+H).

EXAMPLE B56

N-[(1S,2S)-3-(4-Allylcarbamoyl-5,5-dimethyl-thiazolidin-3-yl)-1-benzyl-2-hydroxy-3-oxo-propyl]-nicotinamide

[0767]

270

[0768] White solid: 1H NMR (DMSO-d6) δ 8.81 (d, J=8.6, 1), 8.77 (d, J=6.2, 1H), 8.12 (m, 1H), 7.99 (m, 1H), 7.63 (m, 1H), 7.32-7.12 (m, 7H), 5.78 (m, 1H), 5.18 (m,2H), 4.56(m,3H), 4.40 (m, 4H), 2.87-2.67 (m, 2H), 1.49 (s, 3H), 1.34 (s, 3H); Anal. (C26H32N4O4S.0.5H2O.0.5 TFA) calculated C, (57.65); H, (6.36); N, (10.19). found C, (57.73); H, (5.91); N, (10.15). HRMS (ESI) m/z calcd for 483.2075, found 497.2066.

EXAMPLE B57

3-[(2S,3S)-3-(5-Bromo-thiophene-2-sulfonylamino)-2-hydroxy-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0769]

271

[0770] Isolated yield: 33%. MS-APCI (m/z+): 667 (M+H); HPLC: Rf (min) 20.98; Purity: 97%.

EXAMPLE B58

3-[(2S,3S)-3-(4-Cyano-benzenesulfonylamino)-2-hydroxy-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0771]

272

[0772] Isolated yield: 25%. MS-APCI (m/z+): 607 (M+H); HPLC: Rf (min) 20.71; Purity: 96%.

EXAMPLE B59

3-[(2S,3S)-3-(3-Benzyl-ureido)-2-hydroxy-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0773]

273

[0774] Isolated yield: 69%. 1H NMR (400 MHz, DMSO-d6): δ 8.35 (t, 1H), 7.29 (d, 1H), 7.25-7.6 (m, 13H), 6.31 (t, 1H), 6.18 (d, 1H), 5.11 (d, 1H), 5.01 (d, 1H), 4.95 (d, 1H), 4.48-4.45 (s, 2H), 4.37 (dd, 1H), 4.19-4.03 (m, 4H), 2.70 (d, 1H), 2.53-2.46 (m, partially obscured by DMSO, 1H), 2.24 (s, 3H), 1.49 (s, 3H), 1.33 (s, 3H); MS-APCI (m/z+): 575 (M+H); HPLC: Rf (min.) 20.66; Purity: 97%, C32H38N4O4S.0.4H2O calculated: 66.05, 6.72, 9.63; found: 66.18, 6.70, 9.61.

EXAMPLE B60

3-{(S)-2-Hydroxy-3-[3-(4-methoxy-benzyl)-ureido]-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0775]

274

[0776] Isolated yield: 41%. 1H NMR (400 MHz, DMSO-d6): δ 8.36 (t, 1H), 7.30-7.05 (m, 11H), 7.00 (d, 1H), 6.79 (d 1H), 6.23 (t, 1H), 6.12 (d, 1H), 5.10 (d, 1H), 5.02 (d, 1H), 4.94 (d, 1H), 4.48-4.44 (m, 2H), 4.38 (dd, 1H), 4.14 (dd, 1H), 4.08-3.96 (m, 4H), 3.69 (s, 3H), 2.68 (d, 1H), 2.24 (s, 3H), 1.49 (s, 3H), 1.33 (s, 3H); MS-APCI (m/z+): 605 (M+H).

EXAMPLE B61

3-[(2S,3S)-3-(3-Benzyl-ureido)-2-hydroxy-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid benzylamide

[0777]

275

[0778] Isolated yield: 53%. 1H NMR (400 MHz, DMSO-d6): δ 8.48 (t, 1H), 7.29-7.16 (m, 13H), 7.06 (d, 2H), 6.31-6.25 (m, 2H), 6.17 (d, 1H), 5.14 (d, 1H), 5.00 (d, 1H), 4.95 (d, 1H), 4.47-4.34 (m, 2H), 4.25-4.03 (m, 4H), 2.72 (d, 1H), 1.48 (s, 3H), 1.31 (s, 3H); MS-APCI (m/z+): 561; C31H36N4O4S.0.3H2O calculated: C, 65.77; H, 6.52; N, 9.90, found: C, 65.70; H, 6.50; N, 9.90.

EXAMPLE B62

3-{(2S,3S)-2-Hydroxy-3-[3-(2-methyl-benzyl)-ureido]-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0779]

276

[0780] Isolated yield: 84%. 1H NMR (400 MHz, DMSO-d6): δ 8.36 (t, 1H), 7.30-7.04 (m, 12H), 6.97 (d, 1H), 6.21-6.15 (m, 2H), 5.11 (d, 1H), 5.02 (d, 1H), 4.93 (d, 1H), 4.48-4.44 (m, 2H), 4.39 (dd, 1H), 4.19-4.04 (m, 4H), 2.67 (d, 2H), 2.24 (s, 3H), 2.14 (s, 3H), 1.48 (s, 3H), 1.33 (s, 3H); MS-APCI (m/z+): 589; HPLC: Rf (min) 21.25; Purity: 100%.

EXAMPLE B63

33-{(2S,3S)-2-Hydroxy-3-[3-(4-methoxy-benzyl)-ureido]-4-phenyl-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 4-methoxy-benzylamide

[0781]

277

[0782] Isolated yield: 59%. 1H NMR (400 MHz, DMSO-d6): δ 8.41 (t, 1H), 7.22-7.14 (m, 8H), 7.00 (d, 2H), 6.83-6.77 (m, 3H), 6.23-6.21 (m, 2H), 6.11 (d, 1H), 5.11 (d, 1H), 5.00 (d, 1H), 4.94 (d, 1H), 4.46-4.41 (m, 2H), 4.29-3.96 (m, 4H), 3.69 (s, 3H), 3.65 (s, 3H), 2.68 (d, 1H), 1.47 (s, 3H), 1.28 (s, 3H); MS-APCI (m/z+): 121, 621; HPLC: Rf (min) 20.68; Purity: 98%.

EXAMPLE B64

{(1S,2S)-1-Benzyl-2-hydroxy-3-[4-(4-methoxy-benzylcarbamoyl)-5,5-dimethyl-thiazolidin-3-yl]-3-oxo-propyl}-carbamic Acid prop-2-ynyl Ester

[0783]

278

[0784] Isolated yield: 64%. 1H NMR (400 MHz, DMSO-d6): δ 8.39 (t, 1H), 7.46 (d, 1H), 7.27-7.13 (m, 8H), 6.79 (d, 2H), 5.34 (d, 1H), 4.93 (dd, 2H), 4.50 (s, 2H), 4.40(s, 2H), 4.29 (dd, 1H), 4.14 (dd, 1H), 3.97-3.88 (m, 1H), 3.67 (s, 3H), 2.72-2.58 (m, 2H), 1.48 (s, 3H), 1.27 (s, 3H); MS-APCI (m/z+): 540; HPLC: Rf (min) 19.07; Purity: 100%; C28H33N3O6S.0.4H2O: calcd: C, 61.50; H, 6.23; N, 7.68. found: C, 61.54; H, 6.37; N, 7.63.

EXAMPLE B65

3-[(2S,3S)-2-Hydroxy-3-((S)-2-methyl-butyrylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0785]

279

[0786] Isolated yield: 98%. 1H NMR (400 MHz, DMSO-d6): δ 8.36 (t, 1H), 7.92 (d, 1H), 7.31-7.26 (m, 3H), 7.18-7.08 (m, 6H), 5.19 (d, 1H), 5.10 (d, 1H), 4.92 (d, 1H), 4.48 (s, 1H), 4.40 (dd, 1H), 4.19-4.14 (m, 2H), 2.69-2.57 (m, 2H), 2.26 (s, 3H), 2.13-2.08 (m, 1H), 1.48 (s, 3H), 1.44-1.36 (m, 1H) 1.33 (s, 3H); 1.20-1.14 (m, 1H), 0.75-0.65 (m, 6H): MS-APCI (m/z+): 265, 526 (M+H); C29H39N3O4S: calcd: C, 66.26; H, 7.48; N, 7.99. found: C, 65.93; H, 7.59; N, 7.83.

EXAMPLE B66

3-{(2S,3S)-2-Hydroxy-3-[3-(2-methyl-benzyl)-ureido]-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (pyridin-4-ylmethyl)-amide

[0787]

280

[0788] Isolated yield: 41%. MS-APCI (m/z+): 225, 576; HPLC: Rf (min) 17.93; Purity: 98%; C31H37N5O4S.0.6H2O: calcd: C, 63.48; H, 6.56; N, 11.94; found: C, 63.41; H, 6.44; N, 11.87.

EXAMPLE B67

((1S,2S)-1-Benzyl-3-{5,5-dimethyl-4-[(pyridin-4-ylmethyl)-carbamoyl]-thiazolidin-3-yl}-2-hydroxy-3-oxo-propyl)-carbamic Acid prop-2-ynyl Ester

[0789]

281

[0790] Isolated yield: 22%. 1H NMR (400 MHz, DMSO-d6): δ 8.55 (t, 1H), 8.49 (d 2H), 7.46 (d, 1H), 7.28 (d, 2H), 7.26-7.09 (m, 6H), 5.42 (d, 1H), 4.97 (d, 1H), 4.47-4.38 (m, 5H), 4.93 (d, 1H), 4.23 (dd, 1H), 3.92-3.88 (m, 1H), 2.72-2.56 (m, 2H), 1.51 (s, 3H), 1.33 (s, 3H); MS-APCI (m/z+): 455, 511; HPLC: Rf (min) 16.76; Purity: 100%.

EXAMPLE B68

3-{(2S,3S)-2-Hydroxy-3-[(1-methyl-1H-pyrrole-3-carbonyl)-amino]-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (pyridin-4-ylmethyl)-amide

[0791]

282

[0792] Isolated yield: 21%. 1H NMR (400 MHz, DMSO-d6): δ 8.57 (t, 1H), 8.41 (d 2H), 7.90 (d, 1H), 7.30 (d, 2H), 7.25 (d, 2H), 7.21-7.19 (m, 1H), 7.14 (t, 1H), 7.07 (t, 1H), 6.81-6,78 (m, 2H), 5.95-5.92 (m, 1H), 5.45 (d, 1H), 5.12 (d, 1H), 5.00 (d, 1H), 4.49-4.34 (m, 3H), 4.32-4.29 (m, 1H), 4.22 (dd, 1H), 3.68 (s, 3H), 2.81-2.76 (m, 2H), 1.52 (s, 3H), 1.34 (s, 3H); MS-APCI (m/z+): 536; HPLC: Rf (min) 17.58; Purity: 96%.

EXAMPLE B69

3-{3-[3-(2,4-Dimethyl-benzyl)-ureido]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0793]

283

[0794] Isolated yield: 17%; MS-APCI (m/z+): 603; HPLC: Rf (min) 21.96; Purity: 97%.

EXAMPLE B70

3-{2-Hydroxy-3-[3-(2-methoxy-benzyl)-ureido]-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0795]

284

[0796] Isolated yield: 18%; MS-APCI (m/z+): 605; HPLC: Rf (min) 21.72; Purity: 94%.

EXAMPLE B71

3-{3-[3-(2,4-Difluoro-benzyl)-ureido]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0797]

285

[0798] Isolated yield: 12%; MS-APCI (m/z+): 611; HPLC: Rf (min) 21.00; Purity: 86%.

EXAMPLE B72

3-{3-[3-(2-Bromo-benzyl)-ureido]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0799]

286

[0800] Isolated yield: 16%; MS-APCI (m/z+): 442, 468, 655; HPLC: Rf (min) 21.59; Purity: 94%.

EXAMPLE B73

3-{3-[3-(4-Bromo-benzyl)-ureido]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0801]

287

[0802] Isolated yield: 5%; MS-APCI: 652 (M−H); HPLC: Rf (min) 22.12; Purity: 95%.

EXAMPLE B74

(R)-3-{(2S,3S)-3-[3-(3,4-Dimethoxy-benzyl)-ureido]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0803]

288

[0804] Isolated yield: 24%; MS-APCI (m/z+): 635; HPLC: Rf (min) 19.44; Purity: 88%.

EXAMPLE B75

(R)-3-{(2S,3S)-2-Hydroxy-4-phenyl-3-[3-(3-trifluoromethyl-benzyl)-ureido]-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0805]

289

[0806] Isolated yield: 19%; MS-APCI (m/z+): 643; HPLC: Rf (min) 21.87; Purity: 95%.

EXAMPLE B76

(R)-3-{(2S,3S)-2-Hydroxy-3-[3-(3-methoxy-benzyl)-ureido]-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0807]

290

[0808] Isolated yield: 35% MS-APCI (m/z+): 605; HPLC: Rf (min) 20.63; Purity: 95%.

EXAMPLE B77

(R)-3-{(2S,3S)-3-[2-(2,6-Dichloro-phenoxy)-acetylamino]-2-hydroxy-4-phenyl-butyryl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0809]

291

[0810] Isolated yield: 75%. 1H NMR (400 MHz, DMSO-d6): δ 8.36 (t, 1H), 8.12 (d, 1H), 7.47 (d, 2H), 7.30-7.22 (m, 3H), 7.20-7.06 (m, 7H), 5.49 (d, 1H), 4.96 (d, 1H), 4.94 (d, 1H), 4.48-4.45 (m, 2H), 4.40-4.33 (m, 3H), 4.23-4.14 (m, 2H), 2.78-2.69 (m, 2H), 2.24 (s, 3H), 1.49 (s, 3H), 1.334 (s, 3H); MS-APCI (m/z+): 644, 646. HPLC: Rf (min) 22.23; Purity: 98%.

EXAMPLE B78

(R)-3-{(2S,3S)-2-Hydroxy-4-phenyl-3-[(1-o-tolyl-methanoyl)-amino]-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-indan-1-ylamide

[0811]

292

[0812] IR (neat, cm−) 3311, 3026, 2966, 1655, 1538, 1454, 1222, 1H NMR (DMSO) 68.40-8.25 (m, 2H), 7.40-7.10 (m, 13H), 5.43 (d, J=6.9, 1H), 5.30 (dd, J=15.0, 7.6, 1H), 5.14 (d, J=9.3, 1H), 5.04 (d, J=9.3, 1H), 4.54-4.30 (m, 3H), 3.00-2.60 (m, 4H), 2.42-2.30 (m, 1H), 2.02 (s, 3H), 1.90-1.80 (m, 1H), 1.49 (s, 3H), 1.44 (s, 3H)HRMS (ESI) m/z calcd for C33H38N3O4S (M+H)+ 572.2581, found 572.2583.

EXAMPLE B79

(R)-3-{(2S,3S)-2-Hydroxy-4-phenyl-3-[(1-o-tolyl-methanoyl)-amino]-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (thiophen-2-ylmethyl)-amide

[0813]

293

[0814] IR (neat, cm−) 3306, 3062, 2966, 1651, 1538, 1454, 1369, 1222, 1110, 700, 1H NMR (DMSO) δ 8.54 (t, J=6.0, 1H), 8.21 (d, J=7.9, 1H), 7.40-7.10 (m, 1H), 6.90 (dd, J=5.0, 3.5, 1H), 5.51 (d, J=6.6, 1H), 5.10 (d, J=9.3, 1H), 5.01 (d, J=9.3, 1H), 4.60-4.30 (m, 5H), 2.92-2.62 (m, 2H), 2.04 (s, 3H), 1.48 (s, 3H), 1.32 (s, 3H)HRMS (ESI) m/z calcd for C29H34N3O4S2 (M+H)+ 552.1989, found 552.1991.

EXAMPLE B80

(R)-3-{(2S,3S)-2-Hydroxy-4-phenyl-3-[(1-o-tolyl-methanoyl)-amino]-butanoyl}-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-cyclohex-2-enylamide

[0815]

294

[0816] IR (neat, cm−1) 3316, 2932, 1632, 1530, 1452, 1242, 1109, 1H NMR (DMSO) 88.25 (d, J=8.2, 1H), 7.95 (d, J=7.9, 1H), 7.40-7.05 (m, 9H), 5.80-5.70 (m, 2H), 5.50-5.40 (m, 1H), 5.39 (d, J=6.9, 1H), 5.12 (d, J=9.2, 1H), 5.00 (d, J=9.2, 1H), 4.54-4.20 (m, 3H), 2.90-2.62 (m, 2H), 2.02 (s, 3H), 2.00-1.60 (m, 6H), 1.48 (s, 3H), 1.37 (s, 3H); HRMS (ESI) m/z calcd for C30H38N3O4S (M+H)+ 536.2568, found 536.2583.

EXAMPLE B81

(R)-3-((2S,3S)-3-{[1-(3-Fluoro-2-methyl-phenyl)-methanoyl]-amino}-2-hydroxy-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)--cyclohex-2-enylamide

[0817]

295

[0818] White solid: 1H NMR (DMSO) δ 8.37 (d, J=8.8, 1H), 7.95 (d, J=7.7, 1H), 7.40-6.90 (m, 8H), 5.80-5.70 (m, 2H), 5.50-5.40 (m, 2H), 5.10 (d, J=8.9, 1H), 5.00 (d, J=8.9, 1H), 4.60-4.20 (m, 3H), 2.90-2.60 (m, 2H), 2.00-1.89 (m, 2H), 1.88 (s, 3H), 1.80-1.60 (m, 4H), 1.48 (s, 3H), 1.37 (s, 3H); HRMS (ESI) m/z calcd for C30H37N3O4SF (M+H)+ 554.2502, found 554.2489.

EXAMPLE B82

(R)-3-((2S,3S)-3-{[1-(3-Fluoro-2-methyl-phenyl)-methanoyl]-amino}-2-hydroxy-4-phenyl-butanoyl)-5,5-dimethyl-thiazolidine-4-carboxylic Acid (S)-indan-1-ylamide

[0819]

296

[0820] White solid: 1H NMR (DMSO) δ 8.43 (d, J=8.8, 1H), 8.34 (d, J=7.9, 1H), 7.40-7.10 (m, 11H), 6.95 (d, J=7.2, 1H), 5.47 (d, J=6.8, 1H), 5.30 (dd, J=15.6, 7.9, 1H), 5.13 (d, J=9.2, 1H), 5.04 (d, J=9.2, 1H), 4.50-4.30 (m, 3H), 3.00-2.60 (m, 4H), 2.42-2.30 (m, 1H), 1.89 (s, 3H), 1.90-1.79 (m, 1H), 1.49 (s, 3H), 1.41 (s, 3H); HRMS (ESI) m/z calcd for C33H37N3O4FS (M+H)+ 590.2489, found 590.2486.

EXAMPLE B83

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.4]nonane-4-carboxylic Acid (S)-indan-1-ylamide

[0821]

297

[0822]

1
H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.33 (d, 1H, J=8.1), 8.20 (d, 1H, J=8.4), 7.30-7.13 (m, 9H), 6.94 (t, 1H, J=8.24), 6.76 (d, 1H, J=7.9), 6.54 (d, 1H, J=7.9), 5.40 (d, 1H, J=6.4), 5.29 (m, 1H), 5.13 (d, 1H, J=9.3), 4.98 (d, 1H, J=9.3), 4.60 (s, 1H), 4.51 (m, 1H), 4.40 (m, 1H), 2.96-2.63 (m, 4H), 2.54-2.26 (m, 2H), 2.04-1.68 (m, 8H), 1.79 (s, 3H). Exact mass calculated for C35H40N3O5S (M+H)+ 614.2689, found 614.2678.

EXAMPLE B84

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.5]decane-4-carboxylic Acid (S)-cyclohex-2-enylamide

[0823]

298

[0824]

1
H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.14 (d, 1H, J=8.6), 8.01 (d, 1H, J=7.9), 7.34-7.13 (m, 5H), 6.90 (t, 1H, J=7.9), 6.78 (d, 1H, J=5.3), 6.52 (d, 1H, J=7.3), 5.57-5.72 (m, 1H), 5.48-5.44 (m, 1H), 5.36 (d, 1H, J=7.0), 5.05 (d, 1H, J=9.0), 4.91 (d, 1H, J=9.0), 4.55 (s, 1H), 4.49-4.46 (m, 1H), 4.42-4.28 (m, 2H), 2.79-2.69 (m, 2H), 1.93 (m, 2H), 1.79 (s, 3H), 1.77-1.45 (m, 14H). Exact mass calculated for C33H42N3O5S (M+H)+ 592.2845, found 592.2842.

EXAMPLE B85

(R)-3-[(2S,3S)-2-Hydroxy-3-(4-hydroxy-butyrylamino)-4-phenyl-butyryl]-5,5-dimethyl-thiazolidine-4-carboxylic Acid 2-methyl-benzylamide

[0825]

299

[0826]

1
H NMR (DMSO-d6) δ 8.36 (t, 1H, J=5.9), 7.97 (d, 1H, J=8.2), 7.31-7.09 (m, 9H), 5.23 (d, 1H, J=7.2), 5.05 (d, 1H, J=9.2), 4.92 (d, 1H, J=9.2), 4.48 (s, 1H), 4.44-4.34 (m, 2H), 4.19-4.13 (m, 2H), 3.26-3.20 (m, 2H), 2.72-2.54 (m, 2H), 2.25 (s, 3H), 2.04-1.98 (m, 2H), 1.49 (s, 3H), 1.47-1.38 (m, 2H), 1.34 (s, 3H). (no peak for primary OH) Exact mass calculated for C28H38N3O5S (M+H)+ 528.2532, found 528.2540. Anal. Calcd for C28H37N3O5S.0.3H2O: C, 63.08; H, 7.11; N, 7.88. Found: C, 62.95; H, 6.88; N, 7.56.

[0827] General Methods C

300

[0828] The synthesis of compounds with the general structure 24 is as follows. The boc-protected carboxylic acids 20a-j are coupled to the requisite amines 2 to yield amino amides 23 using a two step process. The process includes treatment of 20 with 2 in the presence of either diphenyl chlorophosphate or EDCI, followed by exposure to HCl or methane sulfonic acid. Final compounds 24 are obtained by a DCC-mediated coupling of 23 and 4 followed by deprotection of the P2 phenol. Final compounds were purified either by flash chromatography or preventive HPLC.

[0829] Additional General Method C

301

[0830] The synthesis of compounds of the general structure 31 (where P2 is not 2-methyl-3-hydroxy benzamide) is as follows. Amino amides of the general structure 23 were coupled to the Boc-acid intermediate 15 using DCC coupling conditions. The resulting intermediate 29 was deprotected under acidic conditions to yield amine of the general structure 30. Final compounds were obtained by modification of amine 30 by methods described in General Methods B section to give P2 amides, ureas, and carbamates.

[0831] Methods used for Synthesis of Compounds with P1 Variations.

[0832] EDCI coupling—To a solution of acid, amine and HOBT in CH2Cl2 was added EDCI and the solution stirred overnight at room temperature. The solution was concentrated in vacuo and the residue dissolved in ethyl acetate and a small portion of water. The solution was washed with saturated NH4Cl (2×), saturated NaHCO3 (2×), brine (1×), dried with MgSO4 and concentrated in vacuo. The crude used without further purification unless otherwise noted.

[0833] DCC coupling—A solution of acid, amine and HOBT was prepared in ethyl acetate. To the solution was then added DCC in an EtOAc solution at 0° C. and the mixture was stirred overnight at room temperature. The mixture was filtered and the filtrate was concentrated in vacuo. The residue dissolved in ethyl acetate washed with saturated NH4Cl (1×), saturated NaHCO3 (1×), brine (1×), dried over Na2SO4 and concentrated in vacuo. The crude was used without further purification unless otherwise noted.

[0834] 4N HCl Boc deprotection—To a solution of Boc-amine in dioxane was added 4N HCl solution in dioxane and the solution stirred overnight at room temperature. The solution was poured into saturated NaHCO3 and the product was extracted into ethyl acetate. The organic solution was washed with brine, dried over Na2SO4 and concentrated in vacuo. The crude was used without further purification unless otherwise noted.

[0835] MeSO3H Boc deprotection—To a solution of Boc-amine in ethyl acetate at 0° C. was added methane sulfonic acid and the solution stirred 3-6 h at room temperature. The solution was cooled to 0° C. and sufficient saturated NaHCO3 was added to quench the acid. The solution was diluted with ethyl acetate, washed with saturated NaHCO3 and brine, dried over Na2SO4 and concentrated in vacuo. The crude used without further purification unless otherwise noted.

[0836] KCN Phenolic acetate deprotection—A solution of phenolic acetate and KCN in ethanol was heated at 50° C. overnight. The solution was concentrated in vacuo. The residue was purified by flash chromatography eluted with 0 to 5% methanol in CH2Cl2 unless otherwise noted. NaOMe/MeOH Phenolic acetate deprotection—0.5 N NaOCH3/MeOH Phenolic acetate deprotection—A solution of phenolic acetate in EtOAc and methanol was cooled to 0° C. in an ice bath. 0.5 N NaOCH3/MeOH was then added dropwise and then stirred at 0° C. for 1.5-2 hrs following addition. Additional EtOAc was then added, the 0.15 N HCl (4.5 eq.) added dropwise. The phases were separated and organic phase washed with 2.5% Na2CO3 aqueous solution, then with 0.1 N HCl/brine (2:1), followed with brine, dried with MgSO4 and concentrated in vacuo. The resulting residue subjected to flash silica gel chromatography to afford the desired product unless otherwise noted.

[0837] HCl/MeOH Phenolic acetate deprotection—To a solution of phenolic acetate in methanol was added 4N HCl in dioxane and the solution stirred at room temperature ca. 4 h. The solution was concentrated in vacuo. The residue was purified by flash chromatography eluted with 0 to 5% methanol in CH2Cl2 unless otherwise noted.

[0838] Fragments of the General Structure 20.

302

303

[0839] Source of Boc-carboxylic Acids 20a-j

[0840] Boc-acids 20a, 20b and 20c were prepared following the procedure of Demange, L.; Menez, A.; Dugave, C. Tet. Lett. 1998, 39, 1169.

[0841] Boc-acid 20d was prepared in the following way.

304

[0842] (2S)-3,3-Dimethyl-4-oxo-N-(9-phenylfluorenyl)proline Methyl Ester (F2):

[0843] The known ketone F1 (Blanco, M.-J.; Sardina, F. J. J. Org. Chem. 1996, 61, 4748)(14.2 g, 37 mmol) was dimethylated following the procedure of Sharma and Lubell (Sharma, R.; Lubell, W. D. J. Org. Chem. 1996, 61, 202) for the benzyl ester analog. The crude was purified by flash chromatography eluted with 0 to 10% ethyl acetate in hexanes. Isolated yield: 7.86 g (52%). 1H NMR (400 MHz, CDCl3): δ 7.74 (d, 1H), 7.67 (d, 1H), 7.43-7.23 (m, 11H), 3.97 (d, 1H), 3.75 (d, 1H), 3.43 (s, 1H), 2.95 (s, 3H), 1.38 (s, 3H), 0.84 (s, 3H); MS-APCI (m/z+): 412, 241.

[0844] (2S)-3,3-Dimethyl-4-oxo-N-(Boc)proline Methyl Ester (F3):

[0845] To a solution of 9-phenylfluorene-protected amine F2 (300 mg, 0.73 mmol) and di-tert-butyl dicarbonate (320 mg, 1.5 mmol) in tetrahydrofuran (50 mL) was added 20 wt % palladium on carbon (100 mg), and the slurry was treated with 50 psi hydrogen gas for 40 h. The solution was filtered and concentrated in vacuo. The crude was purified by chromatography eluted with hexane, 10% ethyl acetate/hexane, and 25% ethyl acetate/hexane. Isolated yield: 182 mg (92%). 1H NMR (400 MHz, CDCl3): δ 4.42 (s)+4.31 (s) (1H), 4.05 (d)+4.01 (d) (1H), 3.96 (d)+3.94 (d) (1H), 3.72 (s, 3H), 1.48 (s)+1.45 (s) (9H), 1.29 (s)+1.27 (s) (3H), 1.07 (s)+1.06 (s) (3H); MS-APCI (m/z+): 172.

[0846] (2S)-4,4-Difluoro-3,3-dimethyl-N-(Boc)proline Methyl Ester (F4):

[0847] A solution of ketone F3 (1.1 g, 4.1 mmol) and diethylaminosulfur trifluoride (4.3 mL, 32 mmol) in anhydrous dichloroethane (40 mL) was heated at 70° C. for 11 h. The solution was then cooled to ambient temperature and poured slowly into ice-cooled satd. NaHCO3 soln (75 mL). The solution was diluted with ethyl acetate (100 mL) and washed with the NaHCO3 soln, water (1×100 mL) and brine (1×100 mL), dried with magnesium sulfate and concentrated in vacuo. The crude was purified by flash chromatography eluted with 0 to 10% ethyl acetate in hexanes. Isolated yield: 0.75 g (63%). 1H NMR (400 MHz, DMSO-d6): δ 4.15 (s)+4.07 (s) (1H), 3.88-3.77 (m, 2H), 3.76 (s)+3.75 (s) (3H), 1.47 (s)+1.41 (s) (9H), 1.27 (s, 3H), 1.06 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −112.8 (dt, J=230, 13 Hz)+−114.2 (dt, J=230, 15 Hz) (1F), −114.2 (dt, J=230, 14 Hz)+−115.1 (dt, J=230, 11 Hz) (1F); MS-APCI (m/z+): 194.

[0848] (2S)-4,4-Difluoro-3,3-dimethyl-N-(Boc)proline (20d):

[0849] To a solution of methyl ester F4 (4.7 g, 16 mmol) in methanol (100 mL) was added a solution of LiOH (6.8 g, 160 mmol) in water (50 mL) and the solution was heated at 50° C. for 14 h. The methanol was removed in vacuo and the remaining solution was diluted with water (200 mL). The aqueous solution was extracted with ether (2×200 mL), acidified with 1N HCl (200 mL) and extracted again with ether (2×200 mL). The combined organics were washed with brine (1×200 mL), dried with magnesium sulfate and concentrated in vacuo. The while solid was dried overnight at 40° C. under vacuum. Isolated yield: 4.3 g (95%). 1H NMR (400 MHz, DMSO-d6): δ 12.95 (bs, 1H), 3.93 (s, 1H), 3.84-3.74 (m, 2H), 1.38 (s)+1.33 (s) (9H), 1.19 (s, 3H), 1.01 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −111.4 (dt, J=227, 13 Hz)+−112.4 (dt, J=227, 13 Hz) (1F), −113.5 (dt, J=227, 14 Hz)+−113.9 (dt, J=227, 15 Hz) (1F); MS-APCI (m/z+): 180.1, (m/z−): 278.

[0850] Boc-acids 20e, 20f, 20g and 20h were prepared following the procedure of Karanewsky, D.; et al. J. Med. Chem. 1990, 33, 1459.

[0851] Boc-acids of the general structure 20i were prepared by the following method.

305

[0852] Example for n=2:

[0853] The known amino thiol (n=2) (Nagasawa, H. T.; et al. J. Med. Chem. 1987, 30, 1373.) (0.78 g, 3.7 mmol) was stirred in H2O (10 mL) at room temp. The mixture was treated with 37% aqueous formaldehyde (0.36 mL, 4.8 mmol) and the result was stirred overnight at room temp. Next, Boc anhydride (0.96 g, 4.4 mmol) was added as a soln. in THF (5 mL). The result was stirred overnight at room temp. The desired product was isolated and purified by acid-base extraction. (2N HCl, sat. bicarb, and EtOAc).

[0854] The result 20i (n 2) was a white solid. Yield: (92%). 1H NMR (CDCl3): δ 4.82-4.35 (m, 3H), 2.21-1.79 (m, 8H), 1.54 (s, 9H).

[0855] Boc-acid 20j was prepared following the procedure of Hursthouse, M. B., et al. J. Chem. Soc. Perkin Trans. 1, 1995, 2419-2425.

[0856] Boc-acid 20k was obtained by mild base hydrolysis of intermediate F3 from the preparation of Boc-acid 20d.

[0857] Specific Method C

EXAMPLE C1

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-pyrrolidine-2-carboxylic Acid 2-methyl-benzylamide

[0858]

306

[0859] The title compound was prepared according to general methods using carboxylic acid 20a (0.96 g, 3.8 mmol), o-methylbenzyl amine (0.57 mL, 4.6 mmol), HOBT (0.62 g, 4.6 mmol), EDCI (0.88 g, 4.6 mmol), CH2Cl2 (50 mL). To give the crude Boc-amide (MS-APCI (m/z+): 355, 255) (1.35 g, 3.8 mmol). The Boc was removed using the general 4N HCl Boc deprotection. 4N HCl in 1,4-dioxane (5 mL), 1,4-dioxane (5 mL). The result was amino amide of general structure 23. Isolated yield: 0.79 g (71%, 2 steps). 1H NMR (400 MHz, DMSO-d6): δ 9.02 (t, 1H), 7.24-7.14 (m, 4H), 4.55 (t, 1H), 4.35 (dd, 1H), 4.30 (dd, 1H), 3.73 (m, 2H), 2.94 (m, 2H), 2.52 (m, 1H), 2.27 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −95.3 (dq, J=235, 15 Hz, 1F), −96.5 (dq, J=235, 12 Hz, 1F); MS-APCI (m/z+): 255.

[0860] Amino amide 23 (100 mg, 0.34 mmol) was coupled to carboxylic acid 4 (140 mg, 0.38 mmol) using the general DCC coupling method outlined above. HOBT (51 mg, 0.38 mmol), DCC (78 mg, 0.38 mmol), TEA (50 μL, 0.36 mmol), CH2Cl2 (10 mL). The crude was purified by chromatography eluted with 10% acetone in CH2Cl2. Isolated yield: 0.13 g (63%). MS-APCI (m/z+): 608. This material was subjected to the general KCN phenolic acetate deprotection conditions (130 mg, 0.21 mmol), KCN (1 mg, 15 mmol), ethanol (10 mL). The crude was precipitated from diethyl ether and ethyl acetate with hexanes at −78° C. Isolated yield: 0.10 g (84%). 1H NMR (400 MHz, DMSO-d6): δ 9.37 (s, 1H), 8.36 (t, 1H), 8.16 (d, 1H), 7.32-7.09 (m, 9H), 6.93 (t, 1H), 6.76 (d, 1H), 6.54 (d, 1H), 5.49 (d, 1H), 4.66 (dd, 1H), 4.34-4.15 (m, 6H), 2.85-2.67 (m, 3H), 2.40 (m, 1H), 2.22 (s, 3H), 1.79 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −98.7 (m, 2F); MS-APCI (m/z+): 566; HPLC Purity: 100%; Rf (min.) 19.01; Anal. C31H33N3O5F2.0.3H2° C., H, N calcd: C, 65.21; H, 5.93; N, 7.36. found: C, 65.11; H, 5.90; N, 7.17.

EXAMPLE C2

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-pyrrolidine-2-carboxylic Acid (S)-indan-1-ylamide

[0861]

307

[0862] White solid; IR (neat, cm−1) 3308, 3070, 2962, 1651, 1585, 1538, 1372, 1259, 1098; 1H NMR (DMSO-d6) δ 9.34 (s, 1H), 8.36 (d, J=8.2, 1H), 8.21 (d, J=7.9, 1H), 7.33-7.14 (m, 9H), 6.96-6.91 (m, 1H), 6.77 (d, J=8.2, 1H), 6.55 (d, J=7.7, 1H), 5.41 (d, J=6.6, 1H), 5.28 (dd, J=15.0, 7.9, 1H), 4.68 (d, J=5.5, 1H), 4.63 (d, J=5.5, 1H), 4.40-4.20 (m, 3H), 3.00-2.62 (m, 4H), 2.50-2.30 (m, 4H), 1.79 (s, 3H); HRMS (ESI) m/z calcd for C32H34N3O5F2 (M+H)+ 578.2467, found 578.2476; Anal. Calcd for C32H33N3O5F2: C, 66.54; H, 5.76; N, 7.27. Found: C, 66.35; H, 5.70; N, 7.20.

EXAMPLE C3

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-pyrrolidine-2-carboxylic Acid (1,2,3,4-tetrahydro-naphthalen-1-yl)-amide

[0863]

308

[0864] IR (neat, cm−1) 3300, 2934, 1651, 1520, 1455, 1368, 1284; 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.35 (d, J=8.2, 1H), 8.21 (d, J=8.2, 1H), 7.34-7.10 (m, 9H), 6.96-6.91 (m, 1H), 6.77 (d, J=8.1, 1H), 6.55 (d, J=7.5, 1H), 5.40 (d, J=6.4, 1H), 5.00-4.90 (m, 1H), 4.65 (d, J=6.2, 1H), 4.63 (d, J=6.2, 1H), 4.40-4.20 (m, 3H), 3.00-2.60 (m, 4H), 2.50-2.40 (m, 2H), 1.90-1.60 (m, 4H), 1.79 (s, 3H); HRMS (ESI) m/z calcd for C33H36N3O5F2 (M+H)+ 592.2623, found 592.2610; Anal. Calcd for C33H35N3O5F2.1H2O: C, 65.01; H, 6.12; N, 6.89. Found: C, 65.07; H, 5.99; N, 6.75.

EXAMPLE C4

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{1[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-pyrrolidine-2-carboxylic Acid (S)-cyclohex-2-enylamide

[0865]

309

[0866] White solid; IR (neat, cm−1) 3002, 2944, 1650, 1535, 1456, 1371, 1282, 1100; 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.18 (d, J=8.2, 1H), 8.01 (d, J=8.2, 1H), 7.35-7.13 (m, 5H), 6.96-6.91 (m, 1H), 6.76 (d, J=8.1, 1H), 6.54 (d, J=7.5, 1H), 5.77-5.73 (m, 1H), 5.49-5.45 (m, 1H), 5.39 (d, J=6.7, 1H), 4.60 (d, J=5.9, 1H), 4.56 (d, J=5.9, 1H), 4.40-4.10 (m, 4H), 2.90-2.60 (m, 4H), 2.50-2.30 (m, 2H), 1.79 (s, 3H), 1.78-1.60 (m, 2H), 1.60-1.38 (m, 2H); HRMS (ESI) m/z calcd for C29H34N3O5F2 (M+H)+ 542.2467, found 542.2460; Anal. Calcd for C29H33N3O5F2.0.75H2O: C, 62.75; H, 6.26; N, 7.57. Found: C, 62.77; H, 6.14; N, 7.37.

EXAMPLE C5

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-pyrrolidine-2-carboxylic Acid 3-fluoro-2-methyl-benzylamide

[0867]

310

[0868] White solid; IR (neat, cm−1) 3310, 1648, 1584, 1531, 1467, 1361, 1284, 1101; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.43 (t, J=5.5, 1H), 8.16 (d, J=7.5, 1H), 7.31-6.90 (m, 9H), 6.76 (d, J=8.2, 1H), 6.54 (d, J=7.3, 1H), 5.33 (d, J=8.9, 1H), 4.67 (d, J=5.7, 1H), 4.64 (d, J=5.7, 1H), 4.38-4.17 (m, 5H), 2.90-2.60 (m, 4H), 2.14 (s, 3H), 1.79 (s, 3H); HRMS (ESI) m/z calcd for C31H33N3O5F3 (M+H)+ 584.2372, found 584.2397; Anal. Calcd for C31H32N3O5F3.1H2O: C, 62.83; H, 5.61; N, 7.09. Found: C, 62.52; H, 5.63; N, 6.76.

EXAMPLE C6

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-pyrrolidine-2-carboxylic Acid 5-fluoro-2-methyl-benzylamide

[0869]

311

[0870] White solid; IR (neat, cm−1) 3310, 1651, 1585, 1531, 1455, 1372, 1283, 1099; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.45 (t, J=5.5, 1H), 8.15 (d, J=7.5, 1H), 7.30-6.90 (m, 9H), 6.76 (d, J=8.2, 1H), 6.55 (d, J=7.7, 1H), 5.54 (d, J=6.2, 1H), 4.68 (d, J=5.6, 1H), 4.65 (d, J=5.6, 1H), 4.40-4.00 (m, 5H), 3.00-2.60 (m, 4H), 2.19 (s, 3H), 1.79 (s, 3H); HRMS (ESI) m/z calcd for C31H33N3O5F3 (M+H)+ 584.2372, found 584.2391; Anal. Calcd for C31H32N3O5F3.1H2O: C, 62.83; H, 5.61; N, 7.09. Found: C, 62.73; H, 5.65; N, 6.77.

EXAMPLE C7

4,4-Difluoro-1-[2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-pyrrolidine-2-carboxylic Acid propylamide

[0871]

312

[0872]

1
H-NMR (400 MHz, dmso-d6): δ 9.30 (s, 1H), 8.13 (d, 1H), 7.87 (t, 1H), 7.35-7.08 (m, 5H), 6.91 (t, 1H), 6.74 (d, 1H), 6.52 (d, 1H), 5.44 (d, 1H), 4.57 (m, 1H), 4.35-4.09 (m, 3H), 2.96 (m, 2H), 2.83 (d, 1H), 2.7 (m, 2H), 2.35 (m, 1H), 1.8 (s, 3H), 1.35 (q, 2H), 0.78 (t, 3H); IR (KBr in cm−1): 3301, 1641, 1524, 1284; MS (APCI, m/z): 504 (M+H), 486, 312, 179.

EXAMPLE C8

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-pyrrolidine-2-carboxylic Acid ((E)-2-methyl-but-2-enyl)-amide

[0873]

313

[0874] White solid; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.13 (d, J=7.9, 1H), 8.02 (t, J=6.0, 1H), 7.33-7.13 (m, 5H), 6.93 (t, J=7.9, 1H), 6.76 (d, J=8.1, 1H), 6.54 (d, J=7.5, 1H), 5.49 (d, J=6.0, 1H), 5.29 (m, 1H), 4.60 (dd, J=9.3, 5.5, 1H), 4.33-4.16 (m, 4H), 3.66 (dd, J=15.2, 5.5, 1H), 3.52 (dd, J=15.2, 5.5, 1H), 2.86-2.66 (m, 3H), 2.37 (dd, J=14.5, 5.5, 1H), 1.79 (s, 3H), 1.50 (s, 6H); HRMS (ESI) m/z calcd for C28H34N3O5F2 (M+H) 530.2467, found 530.2464.

EXAMPLE C9

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-pyrrolidine-2-carboxylic Acid (3-methyl-but-2-enyl)-amide

[0875]

314

[0876] White solid; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.15 (d, J=8.2, 1H), 7.97 (t, J=5.5, 1H), 7.35-7.14 (m, 5H), 6.94 (t, J=7.7, 1H), 6.76 (d, J=8.2, 1H), 6.53 (d, J=6.8, 1H), 5.47 (d, J=6.6, 1H), 5.07 (m, 1H), 4.57 (dd, J=9.2, 5.3, 1H), 4.32-4.15 (m, 4H), 3.70-3.60 (m, 2H), 2.86-2.64 (m, 3H), 2.38 (dd, J=14.1, 5.1, 1H), 1.79 (s, 3H), 1.62 (s, 3H), 1.58 (s, 3H); HRMS (ESI) m/z calcd for C28H34N3O5F2 (M+H)+ 530.2467, found 530.2463.

EXAMPLE C10

4,4-Difluoro-1-[2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-pyrrolidine-2-carboxylic Acid 2-chloro-benzylamide

[0877]

315

[0878]

1
H-NMR (400 MHz, dmso-d6): 9.35 (s, 1H), 9.3 (d, 1H), 8.52 (t, 1H), 8.13 (d, 1H), 7.44-7.09 (m, 9H), 6.91 (t, 1H), 6.74 (d, 1H), 6.48 (d, 1H), 5.35 (d, 1H), 4.65 (m, 1H), 4.44-4.17 (m, 5H), 2.96-2.57 (m, 3H), 2.41 (m, 1H), 1.74 (s, 3H); IR (KBr, cm−1): 3300, 1640, 1522, 1283; MS (APCI, m/z): 586, 588 (M+H), 445, 330, 284.

EXAMPLE C11

4,4-Difluoro-1-[2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-pyrrolidine-2-carboxylic Acid (benzo[1,3]dioxol-5-ylmethyl)-amide

[0879]

316

[0880]

1
H-NMR (400 MHz, dmso-d6): δ 9.35 (s, 1H), 8.38 (t, 1H), 8.13 (d, 1H), 7.35-7.09 (m, 5H), 6.91 (t, 1H), 6.74 (m, 4H), 6.52 (d, 1H), 5.91 (d, 2H), 5.52 (d, 1H), 4.61 (m, 1H), 4.17-4.38 (m, 4H), 4.09 (dd, 1H), 2.87 (d, 1H), 2.70 (q, 2H), 2.38 (dd, 1H), 0.78 (s, 3H); IR (KBr, cm−1): 3299, 1643, 1492, 1445, 1237, 1038; MS (APCI, m/z): 531 (M+H), 340, 225, 180; HPLC: Rf (min.) 18.226; Purity: 95%.

EXAMPLE C12

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butryl]-pyrrolidine-2-carboxylic Acid 3-methoxy-benzylamide

[0881]

317

[0882] Isolated material was subjected to flash silica gel chromatography, eluting with 30% EtOAc/hexanes then with EtOAc/hexanes (4:1) to afford the title compound. Isolated yield: 89%. 1H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.45 (t, 1H), 8.13 (d, 1H), 7.29 (d, 2H), 7.24-7.19 (m, 3H), 7.17-7.14 (m, 2H), 6.92 (t, 1H), 6.82-6.80 (m, 2H), 6.76-6.73 (m, 1H), 6.54 (d, 1H), 5.60-5.50 (m, 1H), 4.64 (dd, 1H), 4.37-4.13 (m, 6H), 3.69 (s, 3H), 2.88-2.67 (m, 3H), 2.41 (dd, 1H), 1.79 (s, 3H); MS-APCI (m/z+): 582. Anal. C31H33N3O6F2.0.2H2O calcd: 63.62, 5.75, 7.18; found: 63.62, 5.93, 6.92.

EXAMPLE C13

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-pyrrolidine-2-carboxylic Acid 4-methoxy-benzylamide

[0883]

318

[0884] Isolated material was subjected to flash silica gel chromatography, eluting with EtOAc/hexanes (1:1) then with EtOAc/hexanes (4:1) to afford the title compound. Isolated yield: 91%. 1H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.40 (t, 1H), 8.14 (d, 1H), 7.30 (d, 2H), 7.21 (d, 2H), 7.17-7.14 (m, 3H), 6.92 (t, 1H), 6.82-6.80 (m, 2H), 6.76-6.73 (m, 1H), 6.54 (d, 1H), 5.60-5.50 (m, 1H), 4.64 (dd, 1H), 4.37-4.13 (m, 6H), 3.69 (s, 3H), 2.88-2.67 (m, 3H), 2.41 (dd, 1H), 1.79 (s, 3H); MS-APCI (m/z+): 582. HPLC: Rf (min.) 18.53; Purity: 100%.

EXAMPLE C14

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-pyrrolidine-2-carboxylic Acid 2-chloro-6-fluoro-benzylamide

[0885]

319

[0886] Isolated material was subjected to flash silica gel chromatography, eluting with EtOAc/hexanes gradient then with 2% MeOH/CH2Cl2 to afford the title compound. Isolated yield: 49%. 1H NMR (400 MHz, DMSO-d6): δ 9.38 (s, 1H), 8.38 (t, 1H), 8.36 (d, 1H), 7.38-7.29 (m, 3H), 7.25-7.13 (m, 5H), 6.93 (t, 1H), 6.75 (d, 1H), 6.53 (d, 1H), 5.37 (d, 1H), 4.62 (dd, 1H), 4.47-4.18 (m, 6H), 2.90-2.64 (m, 3H), 2.35-2.26 (m, 1H), 1.78 (s, 3H); MS-APCI (m/z+): 312, 604. HPLC: Rf (min.) 19.02; Purity: 94%; Anal. C30H29N3O5F2Cl 0.2H2O calcd: 59.30, 4.88, 6.92, found: 59.27, 4.74, 6.69.

EXAMPLE C15

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid 2-methyl-benzylamide

[0887]

320

[0888]

1
H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.30 (t, 1H), 8.17 (d, 1H), 7.33-7.10 (m, 9H), 6.93 (t, 1H), 6.76 (d, 1H), 6.53 (d, 1H), 5.51 (d, 1H), 4.50-4.25 (m, 6H), 4.15 (dd, 1H), 2.86 (d, 1H), 2.68 (t, 1H), 2.26 (s, 3H), 1.79 (s, 3H), 1.18 (s, 3H), 1.01 (s, 3H); 19F NMR (376 MHz, DMSO-d6): 8-107.5 (dt, 1 F), −114.2 (d, 1F); MS-APCI (m/z+): 594; HPLC Purity: 97%.: Rf (min.) 19.47; Anal. C33H37N3O5F2.0.2H2O calcd: C, 66.36; H, 6.31; N, 7.04. found: C, 66.30; H, 6.38; N, 6.75.

EXAMPLE C16

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid (S)-indan-1-ylamide

[0889]

321

[0890]

1
H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.30 (d, 1H), 8.20 (d, 1H), 7.32 (d, 2H), 7.24-7.12 (m, 7H), 6.93 (t, 1H), 6.76 (d, 1H), 6.53 (d, 1H), 5.45 (d, 1H), 5.29 (dd, 1H), 4.46 (dd, 1H), 4.38-4.20 (m, 4H), 2.98-2.74 (m, 3H), 2.67 (t, 1H), 2.42-2.32 (m, 1H), 1.86-1.80 (m, 1H), 1.78 (s, 3H), 1.18 (s, 3H), 1.10 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −109.1 (d, 1F), −113.5 (d, 1F); MS-APCI (m/z+): 606; HPLC Purity: 95%, Rf (min.) 21.30; Anal. C34H37N3O5F2.0.4H2O calcd: C, 66.63; H, 6.22; N, 6.86. found: C, 66.62; H, 6.19; N, 6.79.

EXAMPLE C17

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid prop-2-ynylamide

[0891]

322

[0892] The title compound was purified by flash chromatography eluting with 0 to 5% MeOH/CH2Cl2, another column was run which was eluted with 50 to 100% ethyl acetate/hexanes. 1H NMR (400 MHz, DMSO-d6): δ 9.35 (s, 1H), 8.40 (t, 1H), 8.13 (d, 1H), 7.32 (d, 2H), 7.24 (t, 2H), 7.15 (t, 1H), 6.93 (t, 1H), 6.75 (d, 1H), 6.51 (d, 1H), 5.54 (d, 1H), 4.43 (dd, 1H), 4.36-4.22 (m, 3H), 4.20 (s, 1H), 3.86 (m, 2H), 3.11 (s, 1H), 2.85 (d, 1H), 2.67 (t, 1H), 1.77 (s, 3H), 1.18 (s, 3H), 1.02 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −108.0 (d, 1F), −114.5 (d, 1F); MS-APCI (m/z+): 528, 312; HPLC: Rf (min.) 18.00; Purity: 97%. Anal. C28H31N3O5F2 C, H, N calcd: C, 63.75; H, 5.92; N, 7.96. found: C, 63.67; H, 6.21; N, 7.85.

EXAMPLE C18

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-3,3-dimethyl-pyrrolidine-2-carboxylic Acid 2-chloro-4-fluoro-benzylamide

[0893]

323

[0894] Isolated material was subjected preparative HPLC purification, eluting with EtOAc/hexanes to afford the title compound. 1H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.52 (t, 1H), 8.16 (d, 1H), 7.49 (dd, 1H), 7.40 (d, 1H), 7.28 (d, 2H), 7.24-7.19 (m, 3H), 7.15-7.10 (m, 2H), 6.92 (t, 1H), 6.75 (d, 1H), 6.52 (d, 1H), 5.55 (d, 1H), 4.46 (dd, 1H), 4.39-4.24 (m, 5H), 2.84 (d, 1H), 2.69-2.64 (m, 1H), 1.78 (s, 3H), 1.19 (s, 3H), 1.00 (s, 3H); MS-APCI (m/z+): 312, 632. HPLC: Rf (min.) 16.83; Purity: 93%.

EXAMPLE C19

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-3,3-dimethyl-pyrrolidine-2-carboxylic Acid Propylamide

[0895]

324

[0896]

1
H NMR (400 MHz, DMSO-d6): δ 9.35 (s, 1H), 8.13 (d, 1H), 7.89 (bs, 1H), 7.32 (d, 2H), 7.23 (t, 2H), 7.15 (t, 1H), 6.92 (t, 1H), 6.75 (d, 1H), 6.51 (d, 1H), 5.48 (d, 1H), 4.40 (dd, 1H), 4.34-4.14 (m, 4H), 3.01 (m, 2H), 2.84 (d, 1H), 2.67 (t, 1H), 1.78 (s, 3H), 1.39 (m, 2H), 1.17 (s, 3H), 1.01 (s, 3H), 0.83 (t, 3H); 19F NMR (376 MHz, DMSO-d6): δ −108.3 (d, 1F), −114.0 (d, 1F); MS-APCI (m/z+): 532, 312; HPLC Purity: 100%, Rf (min.) 18.22; Anal. C28H35N3O5F2.0.2H2O calcd, C, 62.84; H, 6.67; N, 7.85. found: C, 62.71; H, 6.65; N, 7.64.

EXAMPLE C20

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid (furan-2-ylmethyl)-amide

[0897]

325

[0898]

1
H NMR (400 MHz, DMSO-d6): δ 9.35 (s, 1H), 8.40 (t, 1H), 8.13(d, 1H), 7.54 (s, 1H), 7.32 (d, 2H), 7.24 (t, 2H), 7.15 (t, 1H), 6.93 (t, 1H), 6.75 (d, 1H), 6.52 (d, 1H), 6.36 (s, 1H), 6.25 (s, 1H), 5.53 (d, 1H), 4.42 (dd, 1H), 4.36-4.24 (m, 6H), 2.85 (d, 1H), 2.68 (t, 1H), 1.79 (s, 3H), 1.16 (s, 3H), 0.97 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −108.2 (d, 1F), −114.3 (d, 1F); MS-APCI (m/z+): 570; HPLC: Rf (min.) 18.73; Purity: 100%. Anal. C30H33N3O6F2 calcd: C, 63.26; H, 5.84; N, 7.38, found: C, 63.35; H, 5.71; N, 7.20.

EXAMPLE C21

4,4-Difluoro-1-[2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid isobutyl-amide

[0899]

326

[0900]

1
H NMR (400 MHz, DMSO-d6): δ 9.35 (s, 1H), 8.14 (d, 1H), 7.90 (t, 1H), 7.33 (d, 2H), 7.23 (t, 2H), 7.15 (t, 1H), 6.93 (t, 1H), 6.76 (d, 1H), 6.52 (d, 1H), 5.46 (d, 1H), 4.41 (dd, 1H), 4.34-4.20 (m, 4H), 2.92-2.80 (m, 3H), 2.67 (t, 1H), 1.78 (s, 3H), 1.67 (m, 1H), 1.18 (s, 3H), 1.02 (s, 3H), 0.83 (d, 6H); 19F NMR (376 MHz, DMSO-d6): δ −108.2 (dt, 1F), −113.9 (d, 1F); MS-APCI (m/z+): 546; HPLC Purity: 100%, Rf (min.) 18.81; Anal. C29H37N3O5F2.0.2H2O calcd: C, 63.42; H, 6.85; N, 7.65. found: C, 63.29; H, 6.77; N, 7.49.

EXAMPLE C22

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid (thiophen-2-ylmethyl)-amide

[0901]

327

[0902]

1
H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.53 (t, 1H), 8.13 (d, 1H), 7.36 (dd, 1H), 7.33 (d, 2H), 7.24 (t, 2H), 7.15 (t, 1H), 6.97 (t, 1H), 6.92 (m, 2H), 6.76 (d, 1H), 6.53 (d, 1H), 5.53 (d, 1H), 4.49-4.26 (m, 6H), 4.23 (s, 1H), 2.88 (d, 1H), 2.69 (dd, 1H), 1.79 (s, 3H), 1.17 (s, 3H), 1.00 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −108.6 (dt, 1F), −114.2 (d, 1F); MS-APCI (m/z+): 586; HPLC Purity: 100%, Rf (min.) 19.07; Anal. C30H33N3O5F2S calcd: C, 61.52; H, 5.68; N, 7.17, found: C, 61.23; H, 5.64; N, 6.90.

EXAMPLE C23

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid (2,2,2-trifluoro-ethyl)-amide

[0903]

328

[0904]

1
H NMR (400 MHz, DMSO-d6): δ 9.35 (s, 1H), 8.66 (t, 1H), 8.14 (d, 1H), 7.31 (d, 2H), 7.24 (t, 2H), 7.15 (t, 1H), 6.93 (t, 1H), 6.75 (d, 1H), 6.51 (d, 1H), 5.56 (d, 1H), 4.45 (dd, 1H), 4.38-4.25 (m, 4H), 4.04-3.94 (m, 1H), 3.90-3.80 (m, 1H), 2.85 (d, 1H), 2.66 (dd, 1H), 1.77 (s, 3H), 1.19 (s, 3H), 1.01 (s, 3H); 19F NMR (376 MHz, DMSO-d6): 8-71.0 (t, J=10 Hz, 3F), −108.0 (dm, J=227 Hz, 1F), −114.6 (d, J=227 Hz, 1F); MS-APCI (m/z+): 572, 312; HPLC Purity: 100%, Rf (min.) 18.98; Anal. C27H30N3O5F5 calcd: C, 56.74; H, 5.29; N, 7.35. found: C, 56.56; H, 5.43; N, 7.15.

EXAMPLE C24

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid (S)-1-benzopyran-4-y

[0905]

329

[0906] Isolated material was subjected to flash silica gel chromatography, eluting with 45% EtOAc/hexanes to afford the title compound. 1H NMR (400 MHz, DMSO-d6): δ 9.35 (s, 1H), 8.47 (d, 1H), 8.20 (d, 1H), 7.33 (d, 2H), 7.23 (t, 2H), 7.17-7.12 (m, 3H), 6.93 (t, 1H), 6.87 (t, 1H), 6.79 (t, 2H), 6.53 (d, 1H), 5.40 (d, 1H), 4.96 (dd, 1H), 4.47 (dd, 1H), 4.34-4.14 (m, 6H), 2.82 (d, 1H), 2.67 (t, 1H), 2.03-1.98 (m, 1H), 1.93-1.89 (m, 1H), 1.79 (s, 3H), 1.17 (s, 3H), 1.12 (s, 3H); MS-APCI (m/z+): 622. HPLC: Rf (min.) 19.65; Purity: 94%; C34H37N3O6F2.0.5H2O calcd: 64.75, 6.07, 6.66, found: 64.77, 6.24, 6.54

EXAMPLE C25

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid 4-methoxy-benzylamide

[0907]

330

[0908] Isolated material was subjected to flash silica gel chromatography, eluting with 45% EtOAc/hexanes to afford the title compound. 1H NMR (400 MHz, DMSO-d6): δ 9.36 (s, 1H), 8.34 (t, 1H), 8.13 (d, 1H), 7.31 (d, 2H), 7.25-7.13 (m, 5H), 6.93 (t, 1H), 6.83 (d, 2H), 6.76 (d, 1H), 6.53 (d, 1H), 5.54 (d, 1H), 4.43 (dd, 1H), 4.34-4.25 (m, 5H), 4.13 (dd, 1H), 3.68 (s, 3H), 2.88 (d, 1H), 2.68 (dd, 1H), 1.79 (s, 3H), 1.17 (s, 3H), 0.99 (s, 3H); MS-APCI (m/z+): 610; C33H37N3O6F2.0.4H2O calcd: 64.25, 6.18, 6.81, found: 64.19, 6.13, 6.73.

EXAMPLE C26

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid (1,3-benzodioxol-5-ylmethyl)-amide

[0909]

331

[0910] Isolated material was subjected to flash silica gel chromatography, eluting with 45% EtOAc/hexanes to afford the title compound. 1H NMR (400 MHz, DMSO-d6): δ 9.33 (s, 1H), 8.35 (t, 1H), 8.12 (d, 1H), 7.29 (d, 2H), 7.21 (t, 2H), 7.12 (t, 1H), 6.91 (t, 1H), 6.81-6.71 (m, 4H), 6.51 (d, 1H), 5.91 (d, 2H), 5.53 (d, 1H), 4.43 (dd, 1H), 4.30-4.23 (m, 5H), 4.07 (dd, 1H), 2.86 (d, 1H), 2.66 (t, 1H), 1.77 (s, 3H), 1.16 (s, 3H), 0.98 (s, 3H); MS-APCI (m/z+): 135, 312, 624. HPLC: Rf (min.) 19.00; Purity: 97%; C33H35N3O7F2.0.6H2O calcd: 62.47, 5.75, 6.62, found, 62.41, 5.65, 6.36.

EXAMPLE C27

(S)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-oxazolidine-4-carboxylic Acid (S)-indan-1-ylamide

[0911]

332

[0912]

1
H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.31 (d, J=8.1, 1H), 8.13 (d, J=9.0, 1H), 7.30-7.13 (m, 9H), 6.94 (t, J=7.9, 1H), 6.76 (d, J=7.9, 1H), 6.55 (d, J=7.5, 1H), 5.72 (d, J=6.2, 1H), 5.46 (d, J=4.0, 1H), 5.31 (dd, J=15.6, 7.7, 1H), 5.24 (d, J=3.9, 1H), 4.36 (m, 1H), 4.19 (m, 1H), 4.16 (s, 1H), 2.94-2.64 (m, 4H), 2.41-2.34 (m, 1H), 1.86-1.77 (m, 1H), 1.77 (s, 3H), 1.29 (s, 3H), 1.27 (s, 3H); HRMS (ESI) m/z calcd for C33H38N3O6 (M+H)+ 572.2761, found 572.2768.

EXAMPLE C28

(4S,5S)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5-methyl-oxazolidine-4-carboxylic Acid (S)-cyclohex-2-enylamide

[0913]

333

[0914]

1
H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.12 (d, J=8.2, 1H), 7.92 (d, J=8.2, 1H), 7.31-7.13 (m, 5H), 6.94 (t, J=7.9, 1H), 6.76 (d, J=7.9, 1H), 6.56 (d, J=7.3, 1H), 5.77-5.73 (m, 1H), 5.66 (d, J=6.4, 1H), 5.51 (d, J=3.7, 1H), 5.50-5.44 (m, 1H), 5.06 (d, J=3.7, 1H), 4.40-4.15 (m, 5H), 2.97-2.65 (m, 2H), 1.94 (m, 2H), 1.79-1.67 (m, 2H), 1.77 (s, 3H), 1.57-1.44 (m, 2H), 1.20 (d, J=6.2, 3H); HRMS (ESI) m/z calcd for C29H36N3O6 (M+H)+ 522.2604, found 522.2623.

EXAMPLE C29

(S)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5,5-dimethyl-oxazolidine-4-carboxylic Acid (S)-cyclohex-2-enylamide

[0915]

334

[0916]

1
H NMR (DMSO-d6) δ 9.36 (s br, 1H), 8.11 (d, J=8.6, 1H), 7.97 (d, J=7.9, 1H), 7.32-7.15 (m, 5H), 6.93 (t, J=7.7, 1H), 6.76 (d, J=8.1, 1H), 6.54 (d, J=7.3 1H), 5.76 (m, 1H), 5.67 (d, J=6.4, 1H), 5.54-5.41 (m, 1H), 5.43 (d, J=3.8, 1H), 5.21 (d, J=3.8, 1H), 4.40-4.28 (m, 2H), 4.19-4.14 (m, 2H), 2.88 (m, 1H), 2.70 (m, 1H), 1.95 (m, 2H), 1.78 (s, 3H), 1.82-1.68 (m, 2H), 1.58-1.45 (m, 2H), 1.28 (s, 3H), 1.22 (s, 3H); HRMS (BSI) m/z calcd for C30H38N3O6 (M+H)+ 536.2761, found 536.2751; Anal. Calcd for C30H37N3O6: C, 67.27; H, 6.96; N, 7.85. Found: C, 67.07; H, 7.00; N, 7.71.

EXAMPLE C30

3-(2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.4]nonane-4-carboxylic Acid 2-methyl-benzamide

[0917]

335

[0918] White solid; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.38 (t, J=5.5, 1H), 8.26 (d, J=8.1, 1H), 7.31-6.85 (m, 10H), 6.76 (d, J=8.1, 1H), 6.53 (d, J=7.7, 1H), 5.54 (d, J=6.4, 1H), 5.12 (d, J=9.2, 1H), 4.95 (d, J=9.2, 1H), 4.55 (s, 1H), 4.50-4.10 (m, 3H), 4.01 (m, 1H), 2.90-2.60 (m, 2H), 2.20 (s, 3H), 2.10-1.85 (m, 4H), 1.81 (s, 3H), 1.80-1.50 (m, 4H); Anal. Calcd for C34H39N3O5S: C, 67.86; H, 6.53; N, 6.98. Found: C, 67.50; H, 6.23; N, 6.70.

EXAMPLE C31

3-(2-Hydroxy-3-{[1-(2-methyl-3-hydroxy-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.5]decane-4-carboxylic Acid 2-methyl-benzylamide

[0919]

336

[0920] White solid; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.36 (t, J=5.5, 1H), 8.28 (d, J=8.1, 1H), 7.34-6.83 (m, 10H), 6.74 (d, J=8.1, 1H), 6.60 (d, J=7.7, 1H), 5.57 (d, J=6.4, 1H), 5.09 (d, J=9.2, 1H), 4.97 (d, J=9.2, 1H), 4.65 (s, 1H), 4.55-4.06 (m, 3H), 4.01 (m, 1H), 2.91-2.50 (m, 2H), 2.22 (s, 3H), 2.10-1.83 (m, 5H), 1.80 (s, 3H), 1.78-1.50 (m, 5H); Anal. Calcd for C35H41N3O5S: C, 68.26; H, 6.71; N, 6.82. Found: C, 68.44; H, 6.53; N, 6.73.

EXAMPLE C32

7-(2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5-thia-7-aza-spiro[3.4]octane-8-carboxylic acid-2-methyl Benzylamide

[0921]

337

[0922] White solid; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.40 (t, J=5.5, 1H), 8.33 (d, J=8.1, 1H), 7.34-6.92 (m, 101H), 6.81 (d, J=8.1, 1H), 6.51 (d, J=7.7, 1H), 5.48 (d, J=6.4, 1H), 5.09 (d, J=9.2, 1H), 4.87 (d, J=9.2, 1H), 4.63 (s, 1H), 4.58-4.17 (m, 3H), 4.05 (m, 1H), 2.89-2.62 (m, 2H), 2.26 (s, 3H), 2.13-1.86 (m, 3H), 1.80 (s, 3H), 1.79-1.50 (m, 3H); Anal. Calcd for C33H37N3O5S: C, 67.44; H, 6.35; N, 7.15. Found: C, 67.57; H, 6.13; N, 7.22.

EXAMPLE C33

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.4]nonane-4-carboxylic Acid Propylamide

[0923]

338

[0924]

1
H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.11 (d, J—8.4, 1H), 7.86 (t, J—5.5, 1H), 7.34-7.13 (m, 5H), 6.93 (t, J=7.7, 1H), 6.80 (d, J=8.1, 1H), 6.52 (d, J=7.3, 1H), 5.44 (d, J=7.0, 1H), 5.08 (d, J—9.0, 1H), 4.95 (d, J=9.3, 1H), 4.47 (s, 1H), 4.44 (m, 2H), 3.04-2.95 (m, 2H), 2.85-2.70 (m, 2H), 1.93 (m, 2H), 1.81-1.61 (m, 6H), 1.80 (s, 3H), 1.31 (m, 2H), 0.82 (t, J=7.3, 3H); HRMS (ESI) m/z calcd for C29H38N3O5S (M+H)+ 540.2532, found 540.2531.

EXAMPLE C34

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.4]nonane-4-carboxylic Acid ((E)-2-methyl-but-2-enyl)-amide

[0925]

339

[0926]

1
H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.08 (d, J=8.1, 1H), 7.92 (t, J=5.7, 1H), 7.33-7.15 (m, 5H), 6.93 (t, J=7.7, 1H), 6.77 (d, J=8.1, 1H), 6.53 (d, J=7.3, 1H), 5.48 (d, J=6.2, 1H), 5.32 (m, 1H), 5.08 (d, J=9.3, 1H), 4.92 (d, J=9.2, 1H), 4.49 (s, 1H), 4.43 (m, 2H), 3.74-3.67 (m, 1H), 3.42 (m, 1H), 2.85-2.72 (m, 2H), 1.98-1.90 (m, 2H), 1.82-1.62 (m, 6H), 1.81 (s, 3H), 1.49-(s, 6H); HRMS (ESI) m/z calcd for C31H40N3O5S (M+H)+ 566.2689, found 566.2685.

EXAMPLE C35

(S)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.4]nonane-4-carboxylic Acid (S)-cyclohex-2-enylamide

[0927]

340

[0928]

1
H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.15 (d, J=8.4, 1H), 7.91 (d, J=7.9, 1H), 7.34-7.12 (m, 5H), 6.96-6.91 (m, 1H), 6.76 (d, J=8.1, 1H), 6.53 (d, J=7.5, 1H), 5.80-5.65 (m, 1H), 5.48-5.40 (m, 1H), 5.36 (d, J=7.2, 1H), 5.10 (d, J=9.2, 1H), 4.94 (d, J=9.2, 1H), 4.54 (s, 1H), 4.50-4.20 (m, 3H), 2.90-2.60 (m, 2H), 2.10-1.82 (m, 4H), 1.79 (s, 3H), 1.78-1.40 (m, 10H); Anal. Calcd for C32H39N3O5S: C, 66.53; H, 6.80; N, 7.27. Found: C, 66.34; H, 6.62; N, 6.96.

EXAMPLE C36

(R)-3-((2S,3S)-2-Hydroxy-3-{1[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.4]nonane-4-carboxylic Acid 5-fluoro-2-methyl-benzylamide

[0929]

341

[0930] White solid; 1H NMR (DMSO-d6) δ 9.37 (s, 1H), 8.38 (t, J=5.5, 1H), 8.26 (d, J=8.1, 1H), 7.31-6.85 (m, 9H), 6.76 (d, J=8.1, 1H), 6.53 (d, J=7.7, 1H), 5.54 (d, J=6.4, 1H), 5.12 (d, J=9.2, 1H), 4.95 (d, J=9.2, 1H), 4.55 (s, 1H), 4.50-4.10 (m, 3H), 4.01 (dd, J=16.0, 5.5, 1H), 2.90-2.60 (m, 2H), 2.20 (s, 3H), 2.10-1.85 (m, 4H), 1.81 (s, 3H), 1.80-1.50 (m, 4H); Anal. Calcd for C34H38N3O5SF: C, 65.51; H, 6.21; N, 6.74. Found: C, 65.50; H, 6.23; N, 6.70.

EXAMPLE C37

(R)-3-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-1-thia-3-aza-spiro[4.4]nonane-4-carboxylic Acid (1,2,3,4-tetrahydro-naphthalen-1-yl)-amide

[0931]

342

[0932] White solid; 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.26 (d, J=8.4, 1H), 8.20 (d, J=8.4, 1H), 7.30-6.89 (m, 10H), 6.76 (d, J=8.1, 1H), 6.54 (d, J=7.3, 1H), 5.36 (d, J=6.8, 1H), 5.12 (d, J=9.2, 1H), 4.98-4.90 (m, 2H), 4.60-4.30 (m, 3H), 2.90-2.60 (m, 4H), 2.07 (s, 3H), 2.05-1.50 (m, 12H); Anal. Calcd for C36H41N3O5S: C, 68.87; H, 6.58; N, 6.69. Found: C, 68.80; H, 6.41; N, 6.60.

EXAMPLE C38

(R)-7-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5-thia-7-aza-spiro[3.4]octane-8-carboxylic Acid Propylamide

[0933]

343

[0934]

1
H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.11 (d, J=8.4, 1H), 7.96 (t, J=5.9, 1H), 7.33-7.13 (m, 5H), 6.93 (t, J=7.9, 1H), 6.76 (d, J=7.3, 1H), 6.53 (d, J=7.5, 1H), 5.41 (d, J=6.9, 1H), 4.96 (d, J=9.3, 1H), 4.92 (d, J=9.5, 1H), 4.50 (s, 1H), 4.45 (d, J=5.1, 1H), 4.37 (m, 1H), 3.03 (m, 2H), 2.82-2.66 (m, 2H), 2.56-2.42 (m, 2H), 2.16-1.80 (m, 4H), 1.80 (s, 3H), 1.39 (m, 2H), 0.82 (t, J=7.5, 3H); HRMS (ESI) m/z calcd for C28H36N3O5S (M+H)+ 526.2376, found 526.2375.

EXAMPLE C39

(R)-7-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-5-thia-7-aza-spiro[3.4]octane-8-carboxylic Acid (S)-cyclohex-2-enylamide

[0935]

344

[0936] White solid; 1H NMR (DMSO-d6) δ 9.38 (s, 1H), 8.18 (d, J=8.2, 1H), 8.07 (d, J=8.1, 1H), 7.36-7.18 (m, 5H), 6.96 (t, J=8.2, 1H), 6.79 (d, J=8.3, 1H), 6.56 (d, J=7.1, 1H), 5.77 (m, 1H), 5.56-5.47 (m, 1H), 5.36 (d, J=7.0, 1H), 5.02 (d, J=9.3, 1H), 4.95 (d, J=9.3, 1H), 4.58 (s, 1H), 4.51 (m, 1H), 4.39-4.31 (m, 2H), 2.75-2.70 (m, 2H), 2.60-2.44 (m, 2H), 2.15 (m, 1H), 2.04-1.88 (m, 5H), 1.82 (s, 3H), 1.80-1.64 (m, 2H), 1.55-1.46 (m, 2H); HRMS (ESI) m/z calcd for C31H38N3O5S (M+H)+ 564.2532, found 564.2523.

EXAMPLE C40

1-{3-[2-(2,6-Dimethyl-phenoxy)-acetylamino]-2-hydroxy-4-phenyl-butyryl}-4,4-difluoro-pyrrolidine-2-carboxylic Acid 2-methyl-benzylamide

[0937]

345

[0938]

1
H NMR (400 MHz, DMSO-d6): δ 8.36 (t, 1H), 8.13 (d, 1H), 7.29 (d, 2H), 7.25-7.08 (m, 7H), 6.99 (d, 2H), 6.91 (dd, 1H), 5.53 (d, 1H), 4.66 (dd, 1H), 4.33-4.10 (m, 7H), 3.94 (d, 1H), 2.86-2.73 (m, 4H), 2.46-2.38 (m, 1H), 2.22 (s, 3H), 2.12 (s, 6H); 19F NMR (376 MHz, DMSO-d6): δ −98.1 (dq, 1F), −100.0 (dq, 1F); MS-APCI (m/z+): 594; HPLC Purity: 100%, Rf (min.) 21.97; Anal. C33H37N3O5F2.0.3H2O calcd: C, 66.16; H, 6.33; N, 7.01. found: C, 66.23; H, 6.57; N, 7.12.

EXAMPLE C41

{(1S,2S)-1-Benzyl-3-[(S)-4,4-difluoro-2-(2-methyl-benzylcarbamoyl)-pyrrolidin-1-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid (S)-(tetrahydro-furan-3-yl) Ester

[0939]

346

[0940] White solid; 1H NMR (DMSO-d6) δ 8.34 (t, J=5.5, 1H), 7.31-7.09 (m, 10H), 5.40 (d, J=7.0, 1H), 4.95 (m, 1H), 4.65 (dd, J=9.2, 5.7, 1H), 4.35-4.09 (m, 5H), 3.81 (m, 1H), 3.75-3.56 (m, 3H), 3.40 (d, J=10.0, 1H), 2.80-2.36 (m, 4H), 2.23 (s, 3H), 2.05-1.95 (m, 1H), 1.81 (m, 1H); HRMS (ESI) m/z calcd for C28H34N3O6F2 (M+H)+ 546.2416, found 546.2418.

EXAMPLE C42

(S)-4,4-Difluoro-1-((2S,3S)-2-hydroxy-3-{[1-(3-hydroxy-2,4-dimethyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-pyrrolidine-2-carboxylic Acid 2-methyl-benzylamide

[0941]

347

[0942] White solid; 1H NMR (DMSO-d6) δ 8.35 (t, J=5.7, 1H), 8.25 (s br, 1H), 8.09 (d, J=7.9, 1H), 7.33-7.08 (m, 9H), 6.85 (d, J=7.7, 1H), 6.53 (d, J=7.5, 1H), 5.49 (d, J=6.2, 1H), 4.67 (dd, J=9.3, 5.5, 1H), 4.35-4.14 (m, 6H), 2.86-2.67 (m, 4H), 2.23 (s, 3H), 2.13 (s, 3H), 1.85 (s, 3H); HRMS (ESI) m/z calcd for C32H36N3O5F2 (M+H)+ 580.2623, found 580.2650.

EXAMPLE C43

3,5-Dimethyl-isoxazole-4-carboxylic Acid {1-benzyl-3-[4,4-difluoro-2-(2-methyl-benzylcarbamoyl)-pyrrolidin-1-yl]-2-hydroxy-3-oxo-propyl}-amide

[0943]

348

[0944] The crude was purified by chromatography eluted with 10% and 20% acetone in CH2Cl2. 1H NMR (400 MHz, DMSO-d6): δ 8.41 (t, 1H), 8.13 (d, 1H), 7.29 (d, 2H), 7.24-7.09 (m, 7H), 5.54 (d, 1H), 4.66 (dd, 1H), 4.40 (dd, 1H), 4.34-4.28 (m, 3H), 4.25-4.18 (m, 2H), 2.87-2.68 (m, 3H), 2.43-2.36 (m, 1H), 2.25 (s, 3H), 2.22 (s, 3H), 2.07 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −98.0 (dq, 1F), −99.9 (dq, 1F); MS-APCI (m/z+): 555;; HPLC Purity: 100%, Rf (min.) 19.63; Anal. C29H32N4O5F2.0.3H2O calcd: C, 62.20; H, 5.87; N, 10.00; found: C, 62.25; H, 6.00; N, 9.65.

EXAMPLE C44

{1-Benzyl-3-[4,4-difluoro-2-(2-methyl-benzylcarbamoyl)-pyrrolidin-1-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid prop-2-ynyl Ester

[0945]

349

[0946] The crude was purified by chromatography eluted with 10% acetone in CH2Cl2. 1H NMR (400 MHz, DMSO-d6): δ 8.37 (t, 1H), 7.53 (d, 1H), 7.28 (d, 2H), 7.24-7.10 (m, 7H), 5.36 (d, 1H), 4.65 (dd, 1H), 4.54-4.42 (m, 2H), 4.35-4.18 (m, 4H), 4.11 (dd, 1H), 3.8 (m, 1H), 3.43 (t, 1H), 2.79-2.69 (m, 2H), 2.59 (dd, 1H), 2.42-2.34 (m, 1H); 19F NMR (376 MHz, DMSO-d6): δ −98.2 (dq, 1F), −99.7 (dq, 1F); MS-APCI (m/z+): 514; HPLC Purity: 92%, Rf (min.) 19.80; Anal. C27H29N3O5F2 calcd: C, 63.15; H, 5.69; N, 8.18. found: C, 63.00; H, 6.02; N, 8.02.

EXAMPLE C45

1-{3-[2-(2,6-Dimethyl-phenoxy)-acetylamino]-2-hydroxy-4-phenyl-butyryl}-4,4-difluoro-pyrrolidine-2-carboxylic Acid Propylamide

[0947]

350

[0948]

1
H-NMR (400 MHz, dmso-d6): 8.09 (d, 1H), 7.91 (t, 1H), 6.8-7.35 (m, 8H), 5.48 (d, 1H), 4.6 (m, 1H), 3.87-4.4 (m, 5H), 3.04 (d, 2H), 2.61-2.87 (m, 3H), 2.35 (m, 1H), 2.35 (s, 3H), 2.13 (s, 6H), 1.4 (q, 2H), 0.8 (t, 3H); IR (KBr in cm−1): 3278, 2931, 1657, 1534, 1449, 1194; MS (APCI, m/z): 531 (M+H), 340, 225, 180; HPLC: Rf (min.) 20.57; Purity: 95%.

EXAMPLE C46

(S)-1-{(2S,3S)-3-[2-(2,6-Dimethyl-phenoxy)-acetylamino]-2-hydroxy-4-phenyl-butyryl}-4,4-difluoro-3,3-dimethyl-pyrrolidine-2-carboxylic Acid 2-methyl-benzylamide

[0949]

351

[0950]

1
H NMR (400 MHz, DMSO-d6): δ 8.33 (t, 1H), 8.14 (d, 1H), 7.33-7.28 (m, 3H), 7.22 (t, 2H), 7.16 (d, 1H), 7.14-7.06 (m, 3H), 7.02-6.86 (m, 2H), 6.91 (t, 1H), 5.50 (d, 1H), 4.36 (dd, 1H), 4.34-4.18 (m, 6H), 4.14 (d, 1H), 3.98 (d, 1H), 2.84-2.70 (m, 2H), 2.25 (s, 3H), 2.13 (s, 6H), 1.19 (s, 3H), 1.02 (s, 3H); 19F NMR (376 MHz, DMSO-d6): δ −109.1 (dt, 1F), −113.3 (dt, 1F); MS-APCI (m/z+): 622; HPLC Purity: 94%, Rf (min.) 23.90; Anal. C35H41N3O5F2 calcd: C, 67.62; H, 6.65; N, 6.76. found: C, 67.54; H, 7.02; N, 7.09.

EXAMPLE C47

{(1S,2S)-1-Benzyl-3-[(S)-5,5-dimethyl-4-(2-methyl-benzylcarbamoyl)-oxazolidin-3-yl]-2-hydroxy-3-oxo-propyl}-carbamic Acid (S)-(tetrahydro-furan-3-yl) Ester

[0951]

352

[0952]

1
H NMR (DMSO-d6) δ 8.29 (t, J=8.7, 1H), 7.25-7.13 (m, 10H), 5.60 (d, J=6.8, 1H), 5.31 (d, J=4.0, 1H), 5.16 (d, J=4.0, 1H), 4.88 (m, 1H), 4.47-4.05 (m, 5H), 3.86 (m, 1H), 3.72-3.54 (m, 3H), 2.80 (m, 1H), 2.60 (m, 1H), 2.26 (s, 3H), 2.04-1.94 (m, 1H), 1.81-1.76 (m, 1H), 1.29 (s, 3H), 1.16 (s, 3H)HRMS (ESI) m/z calcd for C29H38N3O7 (M+H)+ 540.2710, found 540.2706.

EXAMPLE C48

1-[2-Hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-4-oxo-pyrrolidine-2-carboxylic Acid 2-methyl-benzylamide

[0953]

353

[0954] The product was recrystallized from ethyl acetate, ethyl ether and hexanes. 1H NMR (400 MHz, DMSO-d6): δ 9.34 (s, 1H), 8.73 (t, 1H), 8.18 (d, 1H), 7.26-7.05 (m, 9H), 6.92 (t, 1H), 6.75 (d, 1H), 6.51 (d, 1H), 5.56 (d, 1H), 4.75 (s, 1H), 4.55 (d, 1H), 4.40-4.32 (m, 4H), 4.14 (dd, 1H), 2.85 (d, 1H), 2.66 (dd, 1H), 2.23 (s, 3H), 1.75 (s, 3H), 1.11 (s, 3H), 0.94 (s, 3H); MS-APCI (m/z+): 572; HPLC Purity: 100%, Rf (min.) 19.31.

EXAMPLE C49

(3S,4aS,8aS)-2-((2S,3S)-2-Hydroxy-3-{[1-(3-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-decahydro-isoquinoline-3-carboxylic Acid 2-methyl-benzylamide

[0955]

354

[0956] White solid: 1H NMR (DMSO) δ 9.38 (s, 1H), 8.45-8.15 (m, 2H), 7.40-6.40 (m, 12H), 5.18 (d, J=7.0, 1H), 5.00-3.35 (m, 5H), 3.00-1.00 (m, 22H); Anal. Calcd for C36H43N3O5.0.25H2O: C, 71.80; H, 7.28; N, 6.98. Found: C, 71.83; H, 7.40; N, 7.13.

EXAMPLE C50

2-(2-Hydroxy-3-{[1-(-hydroxy-2-methyl-phenyl)-methanoyl]-amino}-4-phenyl-butanoyl)-2-aza-bicyclo[2.2.1]-heptane-3-carboxylic acid-2-methyl-benzylamide

[0957]

355

[0958]

1
I NMR (DMSO) δ 9.34 (s, 1H), 8.25-8.17 (m, 2H), 7.40-7.16 (m, 9H), 6.96 (q, J=7.7, 1H), 6.80 (d, J=7.7, 1H), 6.58 (d, J=7.7, 1H), 4.91 (d, J=5.7, 1H), 4.74 (s, 1H), 4.46-4.00 (m, 5H), 2.85-2.66 (m, 3H), 2.28 (s, 3H), 1.88 (s, 3H), 1.85-1.50 (m, 6H); HRMS (ESI) m/z calcd for C33H37N3O5Na (M+Na)+ 578.2625, found 578.2604.

[0959] General Methods D

356

[0960] The synthesis of compounds with the general structure 27 is as follows. The boc-protected thiazolidine carboxylic acid 1 is converted to amino-ketones 26 with requisite grignard reagents 25 in the presence of oxalyl chloride. Final compounds 27 are obtained by a DCC-mediated coupling of 26 and 4 followed by deprotection of the P2 phenol. Final compounds were purified either by flash chromatography or preparative HPLC.

[0961] Specific Method D

EXAMPLE D1

N-[(1S,2S)-1-Benzyl-3-((R)-5,5-dimethyl-4-pent-4-enoyl-thiazolidin-3-yl)-2-hydroxy-3-oxo-propyl]-3-hydroxy-2-methyl-benzamide

[0962]

357

[0963] The title compound was prepared as follows. (R)-5,5-Dimethyl-thiazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 1 (1.0 g, 3.80 mmol) was dissolved in benzene (10 mL) and cooled to 0° C. with magnetic stirring. Two drops of DMF were added followed by a drop wise addition of oxalyl chloride (0.33 mL, 3.80 mmol). When gas evolution ceased, the solution was concentrated to a yellow/red residue. The material was dissolved in dry THF (10 mL) and cooled to −78° C. with magnetic stirring. The grignard reagent, 3-butenylmagnesium bromide (7.7 mL, 3.80 mmol) was added dropwise over 10 min. The result was stirred at −78° C. for 1 h then at −55° C. for 30 min. The reaction was quenched at −55° C. with sat NH4Cl soln.(3 mL) and then poured into H2O (50 mL). The mixture was extracted with EtOAc (2×50 mL). The combined organics were washed with brine (1×100 mL), dried over Na2SO4, filtered, and concentrated. The result was the amino ketone 26 that was sufficiently pure to use in the subsequent step. The clear oil 26 (0.24 g, 1.15 mmol) was dissolved in EtOAc (10 mL). AMB-AHPBA 4 (0.40 g, 1.09 mmol) was added followed by HOBt (0.15 g, 1.09 mmol). The mixture was stirred at room temperature 1 h, then cooled to 0° C. DCC (0.24 g, 1.15 mmol) was slowly added as solution in EtOAc (6 mL). The mixture was warmed to room temperature and stirred overnight. The mixture was filtered and the filtrate was washed with 1N HCl (10 mL), saturated NaHCO3 (10 mL), brine (10 mL), dried over Na2SO4 and concentrated to give a crude white solid (contaminated with DCU). The DCU was removed by flash chromatography (30% to 50% EtOAc in hexanes) to provide a white solid, which was dissolved in MeOH (2 mL) and treated with 4N HCl in 1,4-dioxane (0.26 mL, 1.1 mmol). The reaction was stirred at room temperature overnight then partitioned between 1N HCl (10 mL) and EtOAc (10 mL). The organic layer. was washed with saturated sat. NaHCO3 (1×25 mL) dried over Na2SO4, filtered, and concentrated to a residue which was purified by flash chromatography (60% EtOAc in hexanes) to provide the title compound as a white amorphous solid: 1H NMR (DMSO-d6) δ 9.36 (s, 1H), 8.23 (d, J=8.1, 1H), 7.35-7.14 (m, 5H), 6.96 (t, J=7.5, 1H), 6.78 (d, J=8.2, 1H), 6.52 (d, J=7.5, 1H), 5.81-5.69 (m. 2H), 5.32 (d, J=9.7, 1H), 5.11-5.91 (m, 3H), 4.40 (m, 3H), 2.89-2.61 (m, 4H), 2.37-2.14 (m, 2H), 1.81 (s, 3H), 1.55 (s, 3H), 1.30 (s, 3H); Anal. Calcd for C28H34N2O5S: C, 65.86; H, 6.71; N, 5.49. Found: C, 65.52; H, 6.55; N, 5.81.

[0964] The following examples were synthesized using the specific method outlined above using the appropriate grignard reagent for the desired compound.

EXAMPLE D2

(R)-3-((2S,3R)-4,4-Difluoro-1-[4-(3-fluoro-phenyl)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-butyryl])-3,3-dimethyl-pyrrolidine-2-carboxylic Acid Allylamide

[0965]

358

[0966] The following represents synthesis of key intermediates for the synthesis of the title compound.

[0967] L-2-tert-Butoxycarbonylamino-3-(3-fluoro-phenyl)-propionic Acid.

[0968] A mixture of L-2-amino-3-(3-fluoro-phenyl)-propionic acid (20.0 g, 110 mmol, 1 eq) in H2O (100 mL) was treated with Na2CO3 (16.2 g, 153 mmol, 1.4 eq) in H2O (40 mL) followed by 1,4-dioxane (100 mL) and cooled to 0 C. The BOC2O was added and the reaction mixture was stirred at ambient temperature for 5 h after which the dioxane was evaporated. H2O (125 mL) was then added and the mixture then washed with Et2O (2×100 mL). The aqueous phase was acidified with 10% citric acid followed by extraction with EtOAc (2×300 mL). The combined EtOAc layers were washed with H2O (2×150 mL), brine (150 mL), dried (Na2SO4) and concentrated to give the acid as a colorless, viscous oil which slowly solidified upon standing (31 g, quant). 1H NMR (CDCl3) 7.33-7.26 (m,1H), 7.00-6.91 (m,3H), 4.96 (s,1H), 4.62 (bs,1H), 3.23 (dd, J=14, 5.3, 2H), 1.44 (s, 9H); Anal Calcd for C14H18NO4F: C, 59.36; H, 6.40; N, 4.94. Found: C, 59.29; H, 6.34; N, 4.90.

[0969] L-[2-(3-Fluoro-phenyl)-1-(methoxy-methyl-carbamoyl)-ethyl]-carbamic acid-tert-butyl Ester.

[0970] To a solution of L-2-tert-butoxycarbonylamino-3-(3-fluoro-phenyl)-propionic acid (30.9 g, 109 mmol) in THF (180 mL) was added carbonyldiimidazole (21.2 g, 131 mmol, 1.2 eq). After stirring the solution at ambient temperature for 45 min was added DMF (64 mL), N,O-dimethylhydroxylamine hydrochloride (11.7 g, 120 mmol, 1.1 eq) and diisopropylethylamine (20 mL, 113 mmol, 1.04 eq). After stirring for a total time of 2 h, the solvents were evaporated in vacuo and the oily residue dissolved in EtOAc (300 mL). The organic phase was washed with H2O (500 mL), 10% citric acid (2×150 mL), H2O (500 mL), sat'd Na2CO3 (200 mL), brine (200 mL), dried (Na2SO4) and concentrated to give the product suitable for further use (31.6 g, 89%). 1H NMR (CDCl3) 7.29-7.22 (m,1H), 6.98-6.89 (m,3H), 5.20 (bs, 1H), 4.96 (bs, 1H), 3.72 (s, 3H), 3.19 (s, 3H), 3.07 (dd, J=13.6, 5.9, 2H), 1.41 (s, 9H). Anal Calcd for C16H23N2O4F: C, 58.88; H, 7.10; N, 8.58. Found: C, 58.89; H, 7.19; N, 8.71.

[0971] L-[1-(3-Fluoro-benzyl)-2-oxo-ethyl]-carbamic Acid tert-butyl Ester.

[0972] To a 3-neck flask which purged with argon was added a 1 M solution of LAH in Et2O (106 mL, 1.1 eq) and cooled to 0 C. A solution of L-[2-(3-fluoro-phenyl)-1-(methoxy-methyl-carbamoyl)-ethyl]-carbamic acid-tert-butyl ester (31.6 g, 97 mmol, 1 eq) in THF (150 mL) was added over a period of 1 h such that the temperature remained below 5 C. After stirring for an additional 30 min the reaction was quenched with EtOAc (60 mL) followed by 5% KHSO4 (100 mL). EtOAc (500 mL) was added and the organic phase was washed with 1N HCl (3×100 mL), H2O (500 mL), brine (200 mL), dried (Na2SO4) and concentrated to a white solid which was filtered and washed with heptane (200 mL). The aldehyde was suitable for further use (17.6 g, 68%). 1H NMR (CDCl3) 9.65 (s, 1H), 7.33-7.26 (m, 1H), 7.01-6.89 (m, 3H), 5.06 (bs, 1H), 4.43 (broad m, 2H), 1.45 (s, 9H). Anal Calcd for C14H18NO3F: C, 62.91; H, 6.79; N, 5.24. Found: C, 62.73; H, 6.66; N, 5.21.

[0973] 3-tert-Butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric Acid (diastereomeric).

[0974] A solution of L-[1-(3-fluoro-benzyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester (17.6 g, 66 mmol, 1 eq) in MeOH (104 mL) was cooled to 0 C. A solution of sodium bisulfite in H2O (104 mL) was added and the mixture stirred for 5 h at 0C after which it was placed in a freezer for 7 h. The reaction mixture was then charged with a solution of NaCN (3.87 g, 79 mmol, 1.2 eq) in H2O (104 mL) followed by EtOAc (280 mL) and stirred at room temperature for 11 h after which the organic layer was separated, dried (Na2SO4) and concentrated to give the crude cyanohydrin as a waxy solid. This material was dissolved in 1,4 dioxane (265 mL), charged with anisole (11 mL) and cooled to 0 C. Concentrated HCl (265 mL) was added, with vigorous stirring, to the reaction mixture followed by heating at reflux for 1 h. The dioxane plus most of the water was evaporated in vacuo. The remaining residue was basified with 2N NaOH and washed with Et2O (3×200 mL). The aqueous phase was then charged with 1,4 dioxane (120 mL) followed by BOC2O (15.8 g, 1.1 eq). After stirring at ambient temperature for 3 h the dioxane was removed in vacuo and the remaining mixture acidified with 10% citric acid followed by extraction with EtOAc (2×300 ml). The combined organic layers were washed with H2O (300 mL), brine (200 mL), dried (Na2SO4) and concentrated to give the acid as diastereomeric mixture (ca 1:1) and orange solid (10.56 g, 51%) 1H NMR (DMSO) 7.35-7.25 (m,2H), 7.06-6.96 (m, 6H), 6.76 (d, J=9.0, 1H), 6.43 (d, J=9.6, 1H), 4.02-3.89 (m, 4H), 3.57 (m, 2H), 2.83 (dd, J=13.4, 6.1, 2H), 1.28 (s, 9H), 1.26 (s, 9H).

[0975] (2S,3R)-3-tert-Butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric Acid Methyl Ester.

[0976] To a solution of 3-tert-butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric acid (diastereomeric) (10.56 g, 33.8 mmol., 1 eq) in DMF (130 mL) was suspended K2CO3 (6.07 g, 43 mmol, 1.3 eq) followed by CH3I (4.2 mL, 68 mmol, 2 eq). After stirring for 2 h at ambient temperature the DMF was evaporated in vacuo. The remaining residue was dissolved in EtOAc (300 mL) and washed with H2O (2×100 mL), sodium thiosulfate solution (100 mL), brine (200 mL) dried (Na2SO4) and concentrated to give a crude orange solid (9.55 g). Purification by column chromatography (1:1 EtOAc/hexanes) afforded 6.96 g total (63%); of which 3.28 g being the desired diastereomer (2S,3R)-3-tert-Butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric acid methyl ester (cream colored solid), and 3.68 g being the undesired product (2R,3R)-3-tert-butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric acid methyl ester. (2S,3R) product: 1H NMR (CDCl3) 7.30-7.22 (m, 1H), 7.01-6.90 (m, 3H), 4.88 (d, J=8.2, 1H), 4.32 (m, 2H), 3.67 (s, 3H), 2.79 (t, J=6.9, 2H), 1.40 (s, 9H). (2R,3R) product: 1H NMR (CDCl3) 7.32-7.25 (m, 1H), 7.09-6.91 (m, 3H), 4.82 (d, J=9.8, 1H), 4.27 (dd, J=16.9, 7.6, 1H), 4.08 (d, J=3.2, 1H), 3.78 (s, 3H), 3.17 (d, J=4.5, 1H), 2.93(d, J=4.5, 1H), 1.40 (s, 9H).

[0977] (2S,3R)-3-tert-Butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric Acid.

[0978] A mixture of (2S,3R)-3-tert-Butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric acid methyl ester (3.28 g, 10.05 mmol, 1 eq), 4N NaOH (4 mL, 16 mmol, 1.6 eq), MeOH (42 mL) and 1,4-dioxane (63 mL) was stirred at ambient temperature for 1.5 h after which the solvents were evaporated. To the residue was added 10% citric acid (100 mL) followed by extraction with EtOAc (100 mL). The organic layer was washed with H2O (100 mL), brine (50 mL), dried (Na2SO4) and concentrated to give the desired product as a cream colored solid (3.06 g, 97%). 1H NMR (DMSO) 7.33-7.26 (m, 1H), 7.02-6.97 (m, 3H), 6.78 (d, J=5.2, 1H), 3.98 (d, J=5.5, 1H), 3.99-3.86 (m, 2H), 2.77-2.82 (m, 2H), 1.27 (s, 9H).

[0979] Conversion of Undesired (2R,3R) diastereomer-methylester to (2S,3R)-3-tert-butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric Acid.

[0980] (2S,3R)-3-tert-Butoxycarbonylamino-2-(2-chloro-acetoxy)-4-(3-fluoro-phenyl)-butyric Acid Methyl Ester.

[0981] A solution of of the (2R,3R)-3-tert-butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric acid methyl ester (8 g, 24.5 mmol, 1 eq), chloroacetic acid (5.79 g, 61.3 mmol, 2.5 eq), and PPh3 (16 g, 61.3 mmol, 2.5 eq) in benzene (340 mL) was cooled to 0 C followed by the addition of diethylazodicarboxylate (9.7 mL, 61.3 mmol, 2.5 eq) over a 20 min period. After the addition, the reaction mixture was stirred at ambient temperature for 2 h after which the reaction mixture was concentrated and the residue purified by column chromatography with 30% EtOAc/hexanes as eluant. Appropriate fractions were combined and concentrated to give a yellow solid which was shaken with heptane and filtered to remove the yellow DEAD residues. The product was thus obtained as a white solid (4.25 g, 43%) 1H NMR (CDCl3) 7.32 (m, 1H), 7.03-6.96 (m, 3H), 5.34 (d, J=3.5, 1H), 4.26 (s, 2H), 4.75-4.5 (series of m, 2H), 3.77 (s, 3H), 2.92 (bd, J=7, 2H), 1.43 (s, 9H).

[0982] (2S,3R)-3-tert-butoxycarbonylamino-4-(3-fluoro-phenyl)-2-hydroxy-butyric Acid.

[0983] A mixture of (2S,3R)-3-tert-butoxycarbonylamino-2-(2-chloro-acetoxy)-4-(3-fluoro-phenyl)-butyric acid methyl ester (4.56 g, 11.3 mmol, 1 eq), 4N NaOH (6.5 mL, 25.9 mmol, 2.3 eq), MeOH (48 mL) and 1.4-dioxane (72 mL) was stirred at ambient temperature for 4 h after which the solvents were removed in vacuo and the residue was charged with H2O (50 mL) and washed with Et2O (100 mL). The aqueous layer was made acidic with 10% citric acid and extracted with EtOAc (2×75 mL). The combined EtOAc layers were washed with H2O (3×50 mL) brine (50 mL), dried (Na2SO4), concentrated, shaken with heptane and filtered to give the desired acid as a white solid (3.3 g, 94%).

[0984]

1
H NMR (DMSO) 9.42 (s, 1H),8.26 (d, J=8.1, 1H), 8.17 (t, J=5.9, 1H), 7.32 (m, 1H), 7.18 (m, 2H), 7.00 (m, 2H), 6.79 (d, J=8.1, 1H), 6.56 (d, J=7.5, 1H), 5.79 (m, 1H), 5.51 (d, J=6.4, 1H), 5.24 (d, J=15.4, 1H),5.06 (d, J=10.4, 1H), 4.49-4.28 (series of m, 5H), 3.74 (broad m, 2H), 2.89-2.67 (m, 2H), 1.81 (s, 3H), 1.22 (s, 3H), 1.05 (s, 3H). Anal Calcd for C28H32N3O5F3x0.25H2O: C, 60.91; H, 5.93; N, 7.61. Found: C, 60.96; H, 6.05; N, 7.20.

EXAMPLE D3

(S)-4,4-Difluoro-1-[(2S,3S)-4-(3-fluoro-phenyl)-2-hydroxy-3-(3-hydroxy-2-methyl-benzoylamino)-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid isobutyl-amide

[0985]

359

[0986] White solid: 1H NMR (DMSO-d6) 9.14 (s, 1H), 8.03 (d, 1H, J=8.3), 7.76 (t, 1H, J=5.8), 7.09 (dd, 1H, J=7.4, 14.4), 6.99 (d, 2H, J=7.6), 6.81-6.73 (m, 2H), 6.58 (d, 1H, J=8.1), 6.34 (d, 1H, J=6.8), 5.23 (d, 1H, J=6.6), 4.25 (dd, 1H, J=12.2, 25.0), 4.15-4.08 (m, 3H), 2.77-2.46 (m, 4H), 1.59 (s, 3H), 1.52-1.43 (m, 1H), 1.00 (s, 3H), 0.83 (s, 3H), 0.65 (d, 6H, J=6.4); HRMS (ESI) m/z calcd for C30H37F3N3O5 (M+H)+ 564.6130, found: 564.2674; Anal. Calcd for C30H36F3N3O5: C, 61.80; H, 6.44; N, 7.46. Found: C, 61.58; H, 6.45; N, 7.34.

EXAMPLE D4

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2,5-dimethyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid Propylamide

[0987]

360

[0988] White solid: 1H NMR (DMSO-d6) 9.17 (s, 1H), 8.04 (d, 1H, J=8.1), 7.85 (t, 1H, J=5.1), 7.29-7.09 (m, 5H), 6.53 (s, 1H), 6.30 (s, 1H), 5.38 (d, 1H, J=6.1), 4.40-4.24 (m, 3H), 4.14 (s, 1H), 3.04-2.90 (m, 2H), 2.77 (d, 1H, J=2.2), 2.65-2.59 (m, 1H), 2.09 (s, 3H), 1.67 (3, 3H), 1.39-1.31 (m, 2H), 1.13 (s, 3H), 0.97 (s, 3H), 0.78 (s, 3H). HRMS (ESI) m/z calcd for C29H38F2N3O5 (M+H)+ 546.6230, found 546.2780; Anal. Calcd for C29H37F2N3O5: C, 63.84; H, 6.84; N, 7.70. Found: C, 63.44; H, 6.82; N, 7.52.

EXAMPLE D5

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2,5-dimethyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid isobutyl-amide

[0989]

361

[0990] White solid: 1H NMR (DMSO-d6) 9.24 (s, 1H), 8.11 (d, 1H, J=8.3), 7.94 (t, 1H, J=5.8), 7.37-7.16 (m, 5H), 6.60 (s, 1H), 6.38 (s, 1H), 5.44 (d, 1H, J=6.3), 4.48-4.29 (m, 3H), 4.25 (s, 1H), 2.94-2.83 (m, 3H), 2.73-2.64 (m, 1H), 2.16 (s, 3H), 1.75 (s, 3H), 1.74-1.65 (m, 1H), 1.21 (s, 3H), 1.05 (s, 3H), 0.86 (d, 6H, J=6.6); HRMS (ESI) m/z calcd for C30H40F2N3O5 (M+H)+ 560.6500, found: 560.2928; Anal. Calcd for C30H39F2N-305: C, 64.38; H, 7.02; N, 7.51. Found: C, 64.09; H, 7.05; N, 7.29.

EXAMPLE D6

(S)-4,4-Difluoro-1-[(2S,3S)-2-hydroxy-3-(3-hydroxy-2,5-dimethyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic Acid (2,2,2-trifluoro-ethyl)-amide

[0991]

362

[0992] (S)-4,4-Difluoro-1-[(2S,3 S)-2-hydroxy-3-(3-hydroxy-2,5-dimethyl-benzoylamino)-4-phenyl-butyryl]-3,3-dimethyl-pyrrolidine-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide White solid: 1H NMR (DMSO-d6) 9.27 (s, 1H), 8.72 (t, 1H, J=6.2), 8.15 (d, 1H, J=8.1), 7.37-7.19 (m, 5H), 6.63 (s, 1H), 6.39 (s, 1H), 5.57 (d, 1H, J=6.3), 4.52-4.33 (m, 4H), 4.10-3.94 (m, 1H), 3.93-3.88 (m, 1H), 2.87 (d, 1H, J=7.3), 2.75-2.69 (m, 1H), 2.19 (s, 3H), 1.77 (s, 3H), 1.25 (s, 3H), 1.06 (s, 3H); HRMS (ESI) m/z calcd for C28H33F3N3O5 (M+H)+ 586.5670, found 586.2340; Anal. Calcd for C28H32F3N3O5 0.4H2O: C, 56.73; H, 5.58; N, 7.09. Found: C, 56.64; H, 5.41; N, 6.94.

[0993] Combinatorial Chemistry Approach to HIV Protease P2′ Inhibitors

[0994] General Method E

363

[0995] The combinatorial building block, 8, is prepared using the following method. The boc-protected thiazolidine carboxylic acid, 1, is treated with allyl bromide in the presence of NaNCO3 to yield the boc-protected thiazolidine allyl ester, 2. Deprotection of boc-protected allyl ester, 2, with HCl (g) in EtOAc gives the HCl salt of the thiazolidine allyl ester amine, 3, which is treated with TEA and coupled to 4 in the presence of HOBT and DCC to give the building block precursor, 5. Deprotection of the building block, 5, with 4N HCl yields the phenol, 6. Loading the building block, 6, on to activated cross-linked trityl chloride polystyrene beads, 7, was accomplished in the following manner. The polystyrene cross-linked trityl alcohol was activated to the trityl chloride, 7, by treatment with 20% acetyl chloride in anhydrous CH2Cl2 at room temperature. The trityl chloride beads were combined with the phenol 6 in the presence of Hunig's base in anhydrous CH2Cl2 to yield the substrate loaded polystyrene beads 8. Intermediates were purified either by flash chromatography or preparative HPLC.

364

[0996] The synthesis of the HIV protease combinatorial library was carried out in the following fashion. The allyl ester was removed by treatment with Pd[PPh3]4 and NMM in anhydrous THF to give carboxylate 9, which was treated with pentafluorophenol, pentafluorophenol trifluoromethyl acetate and pyridine in DMF to yield the pentafluoro ester, 10. The pentafluoro ester 10 was treated with various primary amines in a 96-well plate format to give amides 12. The final products were cleaved from the polystyrene crowns with TFA to give products 13. Each product was analyzed by LCMS and HPLC. The following table typifies compounds synthesized by this combinatorial method.

1TABLE 1Ex-pected%MassObservedInhibi-P2′(LCMS)Masstion

365

582583(MH+)5

366

582583(MH+)5

367

529552(Na+)38

368

528529(MH+)4

369

591614(Na+)18

370

555578(Na+)19

371

611612(MH+)1

372

593594(MH+)6

373

576577(MH+)6

374

635658(Na+)5

375

656656(MH+)8

376

575598(Na+)86

377

525548(Na+)56

378

541564(Na+)63

379

529552(Na+)49

380

565588(Na+)42

381

587610(Na+)54

[0997]

382

[0998] The solid phase combinatorial synthesis of HIV protease inhibitors was performed using the IRORI Directed Sorting Technology. Commercial 4-formyl-3-methoxyphenoxymethyl polystyrene resin 1a (PS-MB-CHO, Argonaut Technologies) or 4-formyl-3,5-dimethoxyphenoxymethyl polystyrene resin 1b (PL-FDMP resin, Polymer Laboratories) was loaded into individual Minikans.

[0999] Step A. Reductive Amination with P2′ Amines

[1000] To separate flasks containing sorted MiniKans was added DCM (3 mL/MiniKan). The appropriate primary P2′ amine (3 eq), sodium triacetoxyborohydride (5 eq), and acetic acid (3 eq) were added, and the mixtures were placed under argon, agitated with periodic venting at room temperature for 1-2 hours, and allowed to react overnight. For resin 1a, the filtrates were poured off and the MiniKans were washed with DCM, MeOH (2×), DCM (2×), Et3N/DCM (1:3, 3×), DCM (2×), MeOH (3×), and DCM (4×). For resin 1b, a washing sequence of DCM, MeOH (2×), DCM (2×), Et3N/DCM (1:3, 3×), DCM (2×), DMF, 1M NaOH/DMF (1:5, 3×), DMF (3×), MeOH (3×), and DCM (3×) was used. The MiniKans were dried under vacuum and taken on in Step B.

[1001] Step B. Peptide Coupling with P1′ Amino Acids

[1002] To separate flasks containing the sorted MiniKans was added DMF (3 mL/MiniKan). The appropriate FMOC-protected amino acid (2.5 eq) and 1-hydroxy-7-azabenzotriazole (HOAT) (3 eq) were added and mixed until dissolved, and 1,3-diisopropylcarbodiimide (DIC) (3 eq) was added. The containers were placed under argon and agitated at room temperature overnight. The filtrates were poured off, and the MiniKans were washed with DMF (3×), MeOH (3×), DCM (2×), and DMF (2×). The MiniKans were taken directly on to Step C.

[1003] Step C. FMOC Deprotection

[1004] A container of MiniKans in DMF and piperidine (25%) with a total reaction volume of 3 mL/MiniKan was agitated under argon at room temperature for 45 minutes. The filtrate was removed, and the reaction procedure was repeated. The MiniKans were filtered and washed with DMF (3×), MeOH (2×), DCM (3×), and DMF, and taken directly on to Step D.

[1005] Step D. Peptide Coupling with FMOC-APNS

[1006] FMOC-Allophenylnorstatine (APNS) (3 eq) was added to the flask of MiniKans in DMF (3 mL/MiniKan). After dissolution, HOAT (3.5 eq) and DIC (3.5 eq) were added. The mixture was placed under argon and agitated at room temperature overnight. The reaction was filtered and the MiniKans were washed with DMF (3×), MeOH (3×), DCM (3×), and DMF. FMOC deprotection was carried out as in Step C, and the MiniKans were washed with DMF (3×), MeOH (2×), DCM (3×), dried under vacuum and taken on to Step E or F.

[1007] Step E. Peptide Coupling with P2 Acids

[1008] To separate flasks containing the sorted MiniKans in DMF (3 mL/MiniKan) was added the appropriate P2 acid (3 eq), HOBT hydrate (4 eq), and (3-(dimethylamino)propyl)ethylcarbodiimide hydrochloride (EDAC) (3.5 eq). The reaction was agitated under argon at room temperature for 3 hours. After filtration, the MiniKans were washed with DMF (3×), MeOH (3×), and DCM (3×), dried under vacuum, and taken on to Step G.

[1009] Step F. Reaction with P2 Isocyanates and Chloroformates

[1010] To separate flasks containing the sorted MiniKans in DCM (3 mL/MiniKan) was added the P2 isocyanate (3 eq) or P2 chloroformate (5 eq) and diisopropylethylamine (10 eq). The containers were agitated under argon at room temperature for 2-4 hours. After filtration, the MiniKans were washed with DCM (3×), MeOH (3×), and DCM (3×), dried under vacuum, and taken on to Step G.

[1011] Step G. Cleavage and Processing of the HIV Analogs

[1012] The individual MinKans were sorted into cleavage racks and a solution of 25% TFA in DCM (3 mL/MinKan) was added. The racks were agitated for 1.5 hours. The individual filtrates and DCM rinses were collected, concentrated, and purified by HPLC to provide the final compounds.

2TABLE 2

383

384

385

386

387

388

389

390

391

392

393

394

395

396

397

398

399

400

401

402

403

404

405

406

407

408

409

410

411

412

413

414

415

416

417

418

419

420

421

422

423

424

425

426

427

428

429

430

431

432

433

434

435

436

437

438

439

440

441

442

443

444

445

446

447

448

449

450

451

452

453

454

455

456

457

458

459

460

461

462

463

464

465

466

467

468

469

470

471

472

473

474

475

476

477

478

479

480

481

482

483

484

485

486

487

488

489

490

491

492

493

494

495

496

497

498

499

500

501

502

503

504

505

506

507

508

509

510

511

512

513

514

515

516

517

518

519

520

521

522

523

524

525

526

527

528

529

530

531

532

533

534

535

536

537

538

539

540

541

542

543

544

545

546

547

548

549

550

551

552

553

554

555

556

557

558

559

560

561

562

563

564

565

566

567

568

569

570

571

572

573

574

575

576

577

578

579

580

581

582

583

584

585

586

587

588

589

590

591

592

593

594

595

596

597

598

599

600

601

602

603

604

605

606

607

608

609

610

611

612

613

614

615

616

617

618

619

620

621

622

[1013]

623

[1014] Scheme 3 Experimental

[1015] The solid phase combinatorial synthesis of HJV protease inhibitors was performed using the IRORI Directed Sorting Technology. Commercial 4-formyl-3-methoxyphenoxymethyl polystyrene resin 1a (PS-MB-CHO, Argonaut Technologies) or 4-formyl-3,5-dimethoxyphenoxymethyl polystyrene resin 1b (PL-FDMP resin, Polymer Laboratories) was loaded into individual Minikans.

[1016] Step A. Reductive Amination with P2′ Amines

[1017] To separate flasks containing sorted MiniKans was added DCM (3 mL/MiniKan). The appropriate primary P2′ amine (3 eq), sodium triacetoxyborohydride (5 eq), and acetic acid (3 eq) were added, and the mixtures were placed under argon, agitated with periodic venting at room temperature for 1-2 hours, and allowed to react overnight. For resin 1a, the filtrates were poured off and the MiniKans were washed with DCM, MeOH (2×), DCM (2×), EBt3N/DCM (1:3, 3×), DCM (2×), MeOH (3×), and DCM (4×). For resin 1b, a washing sequence of DCM, MeOH (2×), DCM (2×), Et3N/DCM (1:3, 3×), DCM (2×), DMF, 1M NaOH/DMF (1:5, 3×), DMF (3×), MeOH (3×), and DCM (3×) was used. The MiniKans were dried under vacuum and taken on in Step B.

[1018] Step B. Peptide Coupling with P1′ Amino Acids

[1019] To separate flasks containing the sorted MiniKans was added DMF (3 mL/MiniKan). The appropriate FMOC-protected amino acid (2.5 eq) and 1-hydroxy-7-azabenzotriazole (HOAT) (3 eq) were added and mixed until dissolved, and 1,3-diisopropylcarbodiimide (DIC) (3 eq) was added. The containers were placed under argon and agitated at room temperature overnight. The filtrates were poured off, and the MiniKans were washed with DMF (3×), MeOH (3×), DCM (2×), and DMF (2×). The MiniKans were taken directly on to Step C.

[1020] Step C. FMOC Deprotection

[1021] A z A container of MiniKans in DMF and piperidine (25%) with a total reaction volume of 3 mL/MiniKan was agitated under argon at room temperature for 45 minutes. The filtrate was removed, and the reaction procedure was repeated. The MiniKans were filtered and washed with DMF (3×), MeOH (2×), DCM (3×), and DMF, and taken directly on to Step D.

[1022] Step D. Peptide Coupling with FMOC-APNS

[1023] FMOC-Allophenylnorstatine (APNS) (3 eq) was added to the flask of MiniKans in DMF (3 mL/MiniKan). After dissolution, HOAT (3.5 eq) and DIC (3.5 eq) were added. The mixture was placed under argon and agitated at room temperature overnight. The reaction was filtered and the MiniKans were washed with DMF (3×), MeOH (3×), DCM (3×), and DMF. FMOC deprotection was carried out as in Step C, and the MiniKans were washed with DMF (3×), MeOH (2×), DCM (3×), dried under vacuum and taken on to Step E or F.

[1024] Step E. Peptide Coupling with P2 Acids

[1025] To separate flasks containing the sorted MiniKans in DMF (3 mL/MiniKan) was added the appropriate P2 acid (3 eq), HOBT hydrate (4 eq), and (3-(dimethylamino)propyl)ethylcarbodiimide hydrochloride (EDAC) (3.5 eq). The reaction was agitated under argon at room temperature for 3 hours. After filtration, the MiniKans were washed with DMF (3×), MeOH (3×), and DCM (3×), dried under vacuum, and taken on to Step G.

[1026] Step F. Reaction with P2 Isocyanates and Chloroformates

[1027] To separate flasks containing the sorted MiniKans in DCM (3 mL/MiniKan) was added the P2 isocyanate (3 eq) or P2 chloroformate (5 eq) and diisopropylethylamine (10 eq). The containers were agitated under argon at room temperature for 2-4 hours. After filtration, the MiniKans were washed with DCM (3×), MeOH (3×), and DCM (3×), dried under vacuum, and taken on to Step G.

[1028] Step G. Cleavage and Processing of the HIV Analogs

[1029] The individual MinKans were sorted into cleavage racks and a solution of 25%

[1030] TFA in DCM (3 mL/MinKan) was added. The racks were agitated for 1.5 hours. The individual filtrates and DCM rinses were collected, concentrated, and purified by HPLC to provide the final compounds.

3TABLE 3

624

625

626

627

628

629

630

631

632

633

634

635

636

637

638

639

640

641

642

643

644

645

646

647

648

649

650

651

652

653

654

655

656

657

658

659

660

661

662

663

664

665

666

667

668

669

670

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

701

702

703

704

705

706

707

708

709

710

711

712

713

714

715

716

717

718

719

720

721

722

723

724

725

726

727

728

729

730

731

732

733

734

735

736

737

738

739

740

741

742

743

744

745

746

747

748

749

750

751

752

753

754

755

756

757

758

759

760

761

762

763

764

765

766

767

768

769

770

771

772

773

774

775

776

777

778

779

780

781

782

783

784

785

786

787

788

789

790

791

792

793

794

795

796

797

798

799

800

801

802

803

804

805

806

807

808

809

810

811

812

813

814

815

816

817

818

819

820

821

822

823

824

825

826

827

828

829

830

831

832

833

834

835

836

837

838

839

840

841

842

843

844

845

846

847

848

849

850

851

852

853

854

855

856

857

858

859

860

861

862

863

864

865

866

867

868

869

870

871

872

873

874

875

876

877

878

879

880

881

882

883

884

885

886

887

888

889

Biological Evaluation

[1031] Cells and Virus

[1032] T-cell lines, CEM-SS, and MT-2, and viruses HIV-1 RF and HIV-1 NL4-3 (pNL4-3) were obtained from the National Institutes of Health (AIDS Research and Reference Reagent Program, Bethesda, Md.). HIV-1 NL4-3(184V/L90M) was derived from a clinical isolate that exhibited the protease inhibitor-resistance associated substitutions 184V and L90M, by cloning of an reverse transcriptase-polymerase chain reaction amplified fragment into the unique Age I and Spe I restriction sites of pNL4-3.

[1033] Cytopathic Effect (CPE) Inhibition Assays

[1034] The ability of compounds to protect cells against HIV infection was measured by the MTT dye reduction method, essentially as described (See Pauwels, R. Balzarini, J. Baba, M. Snoeck, R. Schols, D. Herdewijn, P. Desmyter, J. and De Clercq, E. 1988, “Rapid and automated tetrazolium-based calorimetric assay for the detection of anti-HIV compounds,”. J. Virol. Methods., 20: 309-321 and Weislow, O. S. Kiser, R. Fine, D. L. Bader, J. Shoemaker, R. H. and Boyd, M. R. 1989. “New soluble-formazan assay for HIV-1 cytopathic effects: application to high-flux screening of synthetic and natural products for AIDS-antiviral activity”. J. Natl. Cancer Inst. 81:577-586). Subject cells were infected with test virus at an moi of 0.025 to 0.819 or mock infected with medium only and added at 2×104 cells per well into 96 well plates containing half-log dilutions of test compounds. Six days later, 50 μl of XTT (1 mg/ml XTT tetrazolium, 0.02 nM phenazine methosulfate) was added to the wells and the plate was reincubated for four hours. Viability, as determined by the amount of XTT formazan produced, was quantified spectrophotometrically by absorbance at 450 nm. Data from CPE assays were expressed as the percent of formazan produced in compound-treated cells compared to formazan produced in wells of uninfected, compound-free cells. The fifty percent effective concentration (EC50) was calculated as the concentration of compound that effected an increase in the percentage of formazan production in infected, compound-treated cells to 50% of that produced by uninfected, compound-free cells. The 50% cytotoxicity concentration (CC50) was calculated as the concentration of compound that decreased the percentage of formazan produced in uninfected, compound-treated cells to 50% of that produced in uninfected, compound-free cells. The therapeutic index was calculated by dividing the cytotoxicity (CC50) by the antiviral activity (EC50).

[1035] Susceptibility Assays

[1036] Compounds were tested in phenotypic susceptibility assays at Virologic, Inc., (See Petropoulos C. J., Parkin N. T., Limoli K. L., Lie Y. S., Wrin T., Huang W., Tian H., Smith D., Winslow G. A., Capon D J, Whitcomb J M. 2000, “A novel phenotypic drug susceptibility assay for human immunodeficiency virus type 1,” Antimicrob Agents Chemother 44(4):920-928) or using the assay described here. MT-2 cells were infected with either HIV-1 NL4-3 or HIV-1 NL4-3(184V/L90M) and incubated in the presence of serial 0.5 log dilutions of test compounds. Three days later, culture supernatants were collected and virus production, as determined by p24 ELISA, was assayed. Percent inhibition was calculated as p24 concentration in compound-treated samples as compared to infected, compound-free controls. Inhibition of viral replication is determined by measuring reduction in HIV p24 present in the culture supernatant, using a Beckman-Coulter p24 HIV-1 Ag EIA kit and following the supplied protocol. Absorbance is read on a MRX microplate reader (Dynex Technologies). The EC50 was calculated as the concentration of compound that effected a decrease in the p24 production by infected, compound-treated cells to 50% of that produced by infected, compound-free cells.

[1037] HIV-1 Protease RET Assay

[1038] Ki's for the inhibitors of HIV-1 protease were determined using a resonance energy transfer (RET) assay. A mutant form of this enzyme (Q7S) is used for this assay because it is more stable against auto-proteolysis than the wild-type protein. This enzyme is first partially purified as inclusion bodies from cell lysate. It is then solublized in 8M urea and passed through a Q-Sepharose column (Pharmnacia) for further purification. To refold this protein, samples containing Q7S is dialyzed into 50 mM sodium phosphate pH 7.0, 50 mM NaCl, 10 mM DTT, and 10% glycerol.

[1039] The commercially available peptide substrate (Molecular Probes Cat. # H-2930) RE(EDANS)SQNYPIVQK(DABCYL)R is used to assess activity and Ki's. This peptide is cleaved quantitatively by HIV-1 Pr at the Tyr-Pro bond. The EDANS fluorophore absorbs at 340 nm and emits at 490 nm. The reaction is carried out in a 96 well plate in a total volume of 100 μL and is run for 12 minutes at 37C under steady-state conditions with 5 μM substrate and 2 nM active dimer enzyme concentration. The literature value Km for this substrate and enzyme is 103+/−8 μM (See Matayoshi, et al., “Novel Fluorogenic Substrates for Assaying Retroviral Proteases by Resonance Energy Transfer,” Science 247, 954 (1990)). The buffer for this reaction is 0.1M sodium acetate pH 4.8, 1M NaCl, 1 mM EDTA, 5 mM dithiothreitol, 10% dimethyl sulfoxide and 1 mg/ml bovine serum albumin. Inhibition curves are fit using the Morrison tight binding equation.

4ExampleNo.Ave. Ki (nM)Ave CPE EC50 (mM)EC50 or IC50 (mM)A10.210.029A30.510.156A42.20.27A50.20.148A60.230.036A71.70.113A81.40.451A90.490.1381.081A10<0.10.1040.118*A110.50.144A125.50.127A133.40.4950.921*A140.320.0610.226*A15<0.10.0550.057*A160.430.254A17<0.10.0240.049*A180.30.027A190.210.015A200.160.0350.219*A21<0.10.0490.655*A22<0.10.1380.318A232.60.0170.048*A240.520.466A250.970.125A260.60.168A27<0.10.11A283.40.327A290.310.118A3010.90.586A310.440.062A32<0.10.0120.055*A335.10.749A341.40.386A35<0.10.0160.041*A360.780.343A373.70.416A38<0.10.038A39<0.10.1230.213A40<0.10.040.109A410.170.1450.242A42<0.10.0650.098A432.60.534A441.40.478A45<0.10.0340.048A461.10.469A470.270.196A48<0.10.0370.092A490.490.161A50<0.10.0240.125A51<0.10.1590.05A520.510.456A53<0.10.0280.07A544.51.231A550.210.0540.798A560.270.0420.378A575.61.531A5813% @ 64 nMA590.190.417A6066.6A610.991.061A629.62.261A634.51.189A650% @ 64 nMB10.270.0490.236*B20.350.087B32.50.905B430.707B51.20.314B60.310.0950.405*B7<0.10.2650.333*B80.630.474B91.10.452B100.570.386B110.860.5672.015B129.9>1B1321.458B142.71.661B151.32.305B162.61.566B174.8B180.561.25B191.41.5951.298B202.11.5632.084*B210.910.1090.547*B22120.246B230.150.294B248.30.512B2521>1B262.10.348B270.50.506B284.20.731B290.820.063B300.210.443B314.7>1B320.480.433B33<0.10.0450.604*B341.20.389B35110.564B36<0.10.519B377.40.529B380.160.6B391.90.372B4015.1>1B410.110.268B420.130.155B43<0.10.375B444.80.66B451.10.572B4693B471.91.477B480.831.478B49120B507.4B510.99>3.2B52120B542.31.659B55679B56153B5716% @ 64 nMB58240B592.11.815B601.1>3.2B6116.9B624.2B637.8B640.531.603B654.91.636B665.2B6711.4>3.2B6836B697.7B7021B716.4B726.6B7313B7439B7581B7611.2B77<0.10.1431.633B780.180.557B790.780.53B800.150.4191.383B810.350.878B820.191.286B83<0.10.0090.202B84<0.10.0090.686B851.30.363C10.380.6270.427C30.160.486C40.170.2361.903C50.60.6691.608C62.40.7441.944C730.347C81.50.1521.419C96.3C101.51.289C112.81.308C122.71.768C130.591.184C142.5C15<0.10.0250.057C16<0.10.0190.201C17<0.10.1150.186C18<0.10.1480.618C19<0.10.0550.084C20<0.10.035C21<0.10.0150.081C22<0.10.0150.062C23<0.10.0370.109C24<0.10.0190.074C25<0.10.0310.068C26<0.10.0760.131C270.130.1150.189C288.4C290.180.1421.359C30<0.10.0180.273C310.170.0311.067C32<0.10.0090.19C330.130.0451.27C34<0.10.0220.627C35<0.10.0030.289C36<0.10.050.666C370.610.0271.293C38<0.10.0421.313C39<0.10.0130.404C401.81.599C400.820.1741.796C411.31.433C4243.2C4321C4414.8C453.61.575C46<0.10.407C471.41.382C48<0.10.128C49150C507.90.997D1<0.10.0520.601D2<0.10.016D3<.010.013D4<0.10.009D5<0.10.011D6<0.10.018*IC50 (mM) Data was determined at Virologic Inc against the 46I, 84V, 90M virus

[1040] The following compounds have been prepared according to the procedures described herein and have demonstrated the noted activity:

5MOLSTRUCTUREK1EC50

890

0.10.014

891

892

0.340.04

893

422

894

468

895

152

896

6.8

897

0.10.126

898

14.2

899

900

901

7.6

902

0.10.027

903

904

0.10.041

905

148

906

368

907

908

13.9

909

910

911

912

913

914

0.390.332

915

125

916

6.1

917

0.760.573

918

919

8.1

920

0.250.879

921

6.40.901

922

4.71

923

7.8

924

20.488

925

926

3.8

927

1090.672

928

929

930

11.9

931

0.781

932

3.4

933

4.21

934

4.4

935

8.2

936

0.131.16

937

91.176

938

939

2.31.215

940

941

3.91.232

942

18.1

943

6.71.008

944

945

0.381.109

946

5.4

947

4.31.188

948

949

950

261.23

951

952

7.51.252

953

6.11.281

954

31.293

955

4.7

956

17.21.328

957

4.81.35

958

117

959

960

0.441.431

961

0.11.536

962

6.91.551

963

1.11.552

964

965

108

966

122

967

7.6

968

969

11.5

970

971

6.2

972

973

974

975

108

976

3.71.553

977

978

156

979

0.881.641

980

7.61.756

981

0.321.884

982

1.41.947

983

7.41.957

984

17.12.199

985

986

987

283.2

988

0.891.564

989

990

110

991

18.7

992

158

993

994

995

996

9.42.881

997

9.9

998

17.43.2

999

1000

1001

17.3

1002

1003

3.2

1004

12.63.2

1005

15.13.2

1006

12.9

1007

1853.916

1008

1.44.224

1009

4610

1010

823.2

1011

5.83.2

1012

4.43.2

1013

9.83.2

1014

12.73.2

1015

8.43.2

1016

3.63.2

1017

134

1018

18.43.995

1019

51.75.873

[1041] While the invention has been described in terms of preferred embodiments and specific examples, those skilled in the art will recognize that various changes and modifications can be made through routine experimentation without departing from the spirit and scope of the invention. Thus, the invention should be understood as not being limited by the foregoing detailed description, but as being defined by the appended claims and their equivalents.

	Number	Date	Country
	60297460	Jun 2001	US
	60297729	Jun 2001	US

HIV protease inhibitors, compositions containing the same, their pharmaceutical uses and materials for their synthesis

Information

Publication Number

Date Filed

Date Published

Inventors

CPC

US Classifications

International Classifications

Abstract

Description

Claims

Parent Case Info

Provisional Applications (2)