Patent Application
20110257137
Disclosed herein are new heterocyclic compounds and compositions and their application as pharmaceuticals for the treatment of disease. Methods of inhibition of histamine receptor activity in a human or animal subject are also provided for the treatment of allergic diseases, inflammation, asthma, rhinitis, chronic obstructive pulmonary disease, conjunctivitis, rheumatoid arthritis, and general and localized pruritis.
Histamine, a low molecular weight biogenic amine, is a potent chemical mediator of normal and pathological physiology. Histamine functions as a secreted signal in immune and inflammatory responses, as well as a neurotransmitter. The functions of histamine are mediated through 4 distinct cell surface receptors (H1R, H2R, H3R and H4R). Histamine receptors vary in expression, signaling, function and histamine affinity, and therefore have different potential therapeutic applications (Zhang M, Thurmond R L, and Dunford P J Pharmacology & Therapeutics. 2007).
All 4 histamine receptors are G protein-coupled receptors (GPCRs). Upon histamine or other agonist binding, they activate distinct signaling pathways through different heterotrimeric G proteins. The H1R couples to the Gq family of G proteins, whose primary signaling cascade induces second messenger calcium mobilization from intracellular stores, followed by multiple downstream effects. H1R can also increase cyclic GMP (cGMP) production and activate NFκB, a potent, positive transcriptional regulator of inflammation. The H2R couples to the Gs family of G proteins and increases cyclic AMP (cAMP) formation by stimulating adenylate cyclase, although it can also induce calcium mobilization in some cell types. The H3R mediates its function through Gi/o proteins and decreases cAMP formation by inhibiting adenylate cyclase. Like other Gi/o-coupled receptors, H3R also activates the mitogen-activated protein/extracellular-signal regulated protein (MAP/ERK) kinase pathway. H4R has also been demonstrated to couple to Gi/o proteins, with canonical inhibition of cAMP formation and MAP kinase activation. However, H4R also couples to calcium mobilization in certain cell types. In fact, H4R signaling in mast cells is primarily through calcium mobilization with little to no impact on cAMP formation.
The H1R is expressed in many cell types, including endothelial cells, most smooth muscle cells, cardiac muscle, central nervous system (CNS) neurons, and lymphocytes. H1R signaling causes smooth muscle contraction (including bronchoconstriction), vasodilation, and increased vascular permeability, hallmarks of allergic and other immediate hypersensitivity reactions. In the CNS, H1R activation is associated with wakefulness. Its activation is also associated with pruritus and nociception in skin and mucosal tissues. For many years, the anti-allergic and anti-inflammatory activities of H1R antagonists have been utilized to treat acute and chronic allergic disorders and other histamine-mediated pathologies, such as itch and hives.
The H2R is expressed similarly to the H1R, and can also be found in gastric parietal cells and neutrophils. H2R is best known for its central role in gastric acid secretion but has also been reported to be involved in increased vascular permeability and airway mucus production. Antagonists of H2R are widely used in treating peptic ulcers and gastroesophageal reflux disease. These drugs are also used extensively to reduce the risk of gastrointestinal (GI) bleeding associated with severe upper GI ulcers and GI stress in the inpatient setting.
The H3R is primarily found in the CNS and peripheral nerves innervating cardiac, bronchial, and GI tissue. H3R signaling regulates the release of multiple neurotransmitters, such as acetylcholine, dopamine, serotonin, and histamine itself (where it acts as a CNS autoreceptor). In the CNS, H3R participates in the processes of cognition, memory, sleep, and feeding behaviors. H3R antagonists may be used potentially for treating cognition disorders (such as Alzheimer's disease), sleep and wakefulness disorders, attention disorders, and metabolic disorders (especially related to obesity).
Existence of the H4R was predicted in the early 1990s, but its cloning by multiple groups was not reported until 2000. In contrast to the other histamine receptors, the H4R has a distinctly selective expression profile in bone marrow and on certain types of hematopoietic cells. H4R signaling modulates the function of mast cells, eosinophils, dendritic cells, and subsets of T cells. The H4R appears to control multiple behaviors of these cells, such as activation, migration, and cytokine and chemokine production (Zhang M, Thurmond R L, and Dunford P J Pharmacology & Therapeutics. 2007).
Of the 4 known histamine receptors, H1R, H2R and H4R have been shown clearly to affect inflammation and other immune responses and are proposed therapeutic targets for treating immune and inflammatory disorders (Jutel et al., 2002; Akdis & Simons, 2006). The H1R was the first described histamine receptor, and ligands targeting this receptor were initially developed in the 1930s and in widespread use by the 1940s. Common H1R antagonist drugs currently approved for use include systemic agents such as diphenhydramine (Benadryl, also used topically), cetirizine (Zyrtec), fexofenadine (Allegra), loratadine (Claritin) and desloratadine (Clarinex), and topical agents such as olopatadine (Patanol, Pataday, Patanase), ketotifen, azelastine (Optivar, Astelin) and epinastine (Elestat). Traditional uses have included allergic diseases and reactions such as asthma, rhinitis, and other chronic obstructive pulmonary disorders, ocular disorders such as allergic conjunctivitis, and pruritis of varying etiologies.
However, H1 receptor antagonists have certain deficiencies as therapeutic agents in the treatment of diseases where histamine is an important mediator. First, their effects are often only moderate and reduce allergic symptoms by only 40 to 50%. In particular, H1 receptor antagonists, especially systemic agents, have little to no effect in relieving nasal congestion. In allergic asthma, despite the fact that histamine levels rapidly increase in the airways and in plasma (correlating with disease severity), H1 receptor antagonists have largely failed as a therapeutic strategy, though some effect is seen with administration during the priming phase as opposed to the challenge phase (Thurmond R L et al., Nat Rev Drug Discov, 2008, 7:41-53). Additionally, although the efficacy of H1 receptor antagonists against pruritus in acute urticarias, associated with hives and insect stings, and in chronic idiopathic urticaria is well proven, H1R antagonists are mostly ineffective in the treatment of atopic dermatitis-associated pruritus, with the only modest benefits derived from some first-generation compounds likely a consequence of their sedative properties (Sharpe, G. R. & Shuster, S. Br. I Dermatol. 1993, 129:575-9). Finally, sedation caused by H1R antagonists that cross the blood-brain barrier, among other side effects, limits the utility of many H1R antagonists in diseases for which they would otherwise be efficacious. These deficiencies render H1R antagonists amenable to replacement by or supplementation with other agents.
Consequently, attention has focused on the more recently discovered H4 receptor as a therapeutic target. Given the ability of H4R to modulate the cellular function of eosinophils, mast cells, dendritic cells and T cells (M. Zhang et al., Pharmacol Ther 2007), it is natural to speculate that the H4R may be involved in various inflammatory diseases, and that H4R antagonists would have therapeutic potential (Jutel et al., 2006). Indeed, both in vitro and in vivo evidence has been demonstrated for the utility of H4R antagonists as anti-inflammatory agents in inflammatory bowel disease (IBD) (Sander L E et al., Gut 2006; 55:498-504). The finding that H4 receptor antagonists inhibit histamine-induced migration of mast cells and eosinophils in vitro and in vivo, both of which are important effector cells in the allergic response, raises the possibility that this class of compounds could reduce the allergic hyper-responsiveness developed upon repeated exposure to antigens, which is characterized by an increase in the number of mast cells and other inflammatory cells in the nasal and bronchial mucosa (Fung-Leung W P et al., Curr Opin Inves Drugs, 2004 5:11 1174-1182). In contrast to some of the H1R antagonists, H4R antagonists given during the allergen challenge phase of a mouse model of asthma are equally effective to those given during sensitization (Thurmond R L et al., Nat Rev Drug Discov, 2008, 7:41-53). In two recent mouse studies, a selective H4R agonist was shown to induce itch, whereas these responses, and those of histamine, were blocked by pretreatment with H4R antagonists. Similarly, histamine or H4 receptor agonist-induced itch was markedly attenuated in H4 receptor-deficient animals (Dunford, P. J. et al., J. Allergy Clin. Immunol, 2007, 119:176-183). The presence of the H4R in nasal tissue was first discovered by Nakaya et al. (Nakaya, M. et al., Ann Otol Rhinol Laryngol, 2004, 113: 552-557). In addition, a more recent finding showed that there is a significant increase in the level of H4R in human nasal polyp tissue taken from patients with chronic rhinosinusitis (infection of the nose and nasal cavities) when compared to normal nasal mucosa. Jóküti et al. suggest that the administration of H4R antagonists might be a new way to treat nasal polyps and chronic rhinosinusitis. The administration of H4R antagonists may prevent the accumulation of eosinophils as a result of impaired cell chemotaxis toward polypous tissue (Jóküti, A. et al., Cell Biol Int, 2007, 31: 1367). Although scientific data on the role of the H4R in rhinitis is limited, at present, it is the only indication for which an H4R inverse agonist (CZC=13788) is reported to be in preclinical development (Hale, R. A. et al., Drug News Perspect, 2007, 20: 593-600).
Current research efforts include both a focus on H4R selective agents and an alternate path toward dual H1R/H4R agents. Johnson & Johnson have developed a well-characterized H4R antagonist, JNJ-7777120, which is 1000-fold selective over H1, H2, and H3 receptors, and equipotent across human and several nonhuman species. An exemplary H1R/H4R dual agent has yet to publish as of the time of this writing, and the ideal proportion of H1R versus H4R antagonism is a nascent topic of debate. Nevertheless, the concept of dual activity via a single agent is well-precedented, and the design of multiply active ligands is a current topic in pharmaceutical discovery (Morphy R and Rankovic Z, J Med. Chem. 2005; 48(21):6523-43). Additional reports have shown potential for H4R antagonists, or potentially, H1R/H4R dual antagonists, in the treatment of metabolic disorders such as obesity (Jorgensen E et al., Neuroendocrinology. 2007; 86(3):210-4), vascular or cardiovascular diseases such as atherosclerosis (Tanihide A et al., TCM 2006: 16(8): 280-4), inflammation and pain (Coruzzi G et al., Eur J Pharmacol. 2007 Jun. 1; 563(1-3):240-4), rheumatoid arthritis (Grzybowska-Kowalczyk A et al., Inflamm Res. 2007 April; 56 Suppl 1:S59-60) and other inflammatory and autoimmune diseases including systemic lupus erythematosus (Zhang M, Thurmond R L, and Dunford P J Pharmacology & Therapeutics. 2007). What is clear is that a need still exists in the art for improved and varied antihistamines for the treatment of disease, and that compounds with H4R and/or H1R/H4R antagonist activity may fill this need.
Histamine is reportedly implicated in allergic rhinitis by acting on three HR subtypes, the H1R, H3R and H4R. For many years, the classical application of H1R antagonists (antihistamines) has been the treatment of allergic rhinitis. H1R antagonists relieve edema and vasoconstriction, both important symptoms of the disease, but these drugs do not affect the underlying inflammatory responses. After the discovery of the H3R and H4R subtypes, the traditional role for H1R antagonists in rhinitis has been reappraised. It has been shown that the H3R agonist (R)-α-methyl-histamine can induce the dilatation of nasal blood vessels and that this effect can be counteracted by the H3R antagonist/H4R agonist clobenpropit (Taylor-Clark, T., et al, Pulm Pharm Ther, 2008, 21: 455-460). Although a role for the H4R cannot be ruled out, this H3R antagonist-mediated mechanism in nasal decongestion has certainly caught the attention of scientists from Pfizer Inc. Recently, patient recruitment started for a Phase II clinical trial to test a H3R antagonist (PF-03654746, unpublished structure) as a novel nasal decongestant in patients with seasonal allergic rhinitis. A dual target approach is being pursued by GSK that is currently recruiting patients to test a systemic H1/H3 antagonist (GSK835726, unpublished structure) for seasonal allergic rhinitis in a Phase I clinical trial. A second Phase I trial with another H1/H3 antagonist (GSK1004723, unpublished structure) for intranasal administration to treat rhinitis has recently been completed. With these compounds, the mode of action of the classical H1R antagonist is combined with the potential clinical benefit of added nasal decongestion by H3R blockade. The synergistic role of the H1R and H3R has been demonstrated in vivo in experiments performed at Schering-Plough. In view of the role of the H4R in allergic rhinitis, other potential treatment paradigms may also be considered, such as combining H1/H4, H3/H4 or even H1/H3/H4 antagonists/inverse agonist activity in the same molecule approach is being pursued by GSK that is currently recruiting patients to test a systemic H1/H3 antagonist (GSK835726, unpublished structure) for seasonal allergic rhinitis in a Phase I clinical trial. A second Phase I trial with another H1/H3 antagonist (GSK1004723, unpublished structure) for intranasal administration to treat rhinitis has recently been completed. With these compounds, the mode of action of the classical H1R antagonist is combined with the potential clinical benefit of added nasal decongestion by H3R blockade. The synergistic role of the H1R and H3R has been demonstrated in vivo in experiments performed at Schering-Plough. In view of the role of the H4R in allergic rhinitis, other potential treatment paradigms may also be considered, such as combining H1/H4, H3/H4 or even H1/H3/H4 antagonists/inverse agonist activity in the same molecule.
Novel compounds and pharmaceutical compositions, certain of which have been found to inhibit the histamine type-1 receptor (H1R) and/or the histamine type-4 receptor (H4R) have been discovered, together with methods of synthesizing and using the compounds including methods for the treatment of histamine receptor-mediated diseases in a patient by administering the compounds.
Provided herein are compounds of structural Formula (I), or a salt thereof, wherein
or a salt thereof, wherein:
A is an optionally substituted 5- or 6-membered, aromatic heterocycle;
X1 and X5 are independently chosen from C, CH and N;
X6 is chosen from CH and N;
Y1 is chosen from a bond, lower alkyl, lower alkoxy, OR15, NR16R17, and lower aminoalkyl;
R1 is selected from the group consisting of:
aryl, heterocycloalkyl, cycloalkyl, and heteroaryl, any of which may be optionally substituted, when Y1 is a bond; and
null, when Y1 is chosen from OR15, NR16R17, lower alkyl, lower alkoxy, or lower aminoalkyl;
R2, R3, R4, and R5 are independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, C(O)OR24, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
R15 and R16 are independently chosen from aminoalkyl, alkylaminoalkyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, ether, heterocycloalkyl, lower alkylaminoheterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
R17 is independently chosen from hydrogen, aminoalkyl, alkylaminoalkyl aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, ether, heterocycloalkyl, lower alkylaminoheterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; and
R24 is chosen from hydrogen and lower alkyl.
Also provided herein are compounds of structural Formula (II), or a salt thereof, wherein
the ring comprising X1-X5 is aromatic;
X1 and X5 are independently chosen from C, CH and N;
X2 is chosen from [C(R6)(R7)]1, NR8, O and S;
X3 is chosen from [C(R9)(R10)]m, NR11, O, and S;
X4 is chosen from [C(R12)(R13)], NR14, O and S;
n and m are each an integer from 1 to 2;
Y1 is chosen from a bond, lower alkyl, lower alkoxy, OR15, NR16R17, and lower aminoalkyl;
R1 is selected from the group consisting of:
aryl, heterocycloalkyl, cycloalkyl, and heteroaryl, any of which may be optionally substituted, when Y1 is a bond; and
null, when Y1 is chosen from OR15, NR16R17, lower alkyl, lower alkoxy, or lower aminoalkyl;
R2, R3, R4, and R5 are independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
R6, R7, R9, R10, R12, and R13 are independently chosen from null, hydrogen, alkyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
R8, R11, and R14 are independently chosen from null, hydrogen, alkyl, heteroalkyl, alkoxy, haloalkyl, perhaloalkyl, aminoalkyl, C-amido, carboxyl, acyl, hydroxy, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
R15 and R16 are independently chosen from aminoalkyl, alkylaminoalkyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, ether, heterocycloalkyl, lower alkylaminoheterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; and
R17 is independently chosen from hydrogen, aminoalkyl, alkylaminoalkyl aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, ether, heterocycloalkyl, lower alkylaminoheterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted.
Certain compounds disclosed herein may possess useful histamine receptor inhibitory activity, and may be used in the treatment or prophylaxis of a disease or condition in which H1R and/or H4R plays an active role. Thus, in broad aspect, certain embodiments also provide pharmaceutical compositions comprising one or more compounds disclosed herein together with a pharmaceutically acceptable carrier, as well as methods of making and using the compounds and compositions. Certain embodiments provide methods for inhibiting H1R and/or H4R. Other embodiments provide methods for treating a H1R- and/or H4R-mediated disorder in a patient in need of such treatment, comprising administering to said patient a therapeutically effective amount of a compound or composition according to the present invention. Also provided is the use of certain compounds disclosed herein for use in the manufacture of a medicament for the treatment of a disease or condition ameliorated by the inhibition of H1R and/or H4R.
In certain embodiments provided herein,
X1 and X5 are independently chosen from C and N;
X2 is chosen from [C(R6)(R7)]n, NR8, and O;
X3 is chosen from [C(R9)(R10)]m, NR11, and O;
X4 is chosen from NR14, O, and S; and
Y1 is chosen from bond, OR15, and NR16R17; R1 is selected from the group consisting of:
null, when Y1 is chosen from OR15 and NR16R17; and
optionally substituted heterocycloalkyl, when Y1 is a bond.
In certain embodiments provided herein, R8, R11, and R14 are independently chosen from null, hydrogen, and C1-C3 alkyl.
In other embodiments provided herein,
Y1 is bond;
X4 is NR14;
R1 is heterocycloalkyl; and
R14 is null.
Also provided herein are compounds of structural Formula (III), or a salt thereof, wherein,
X2 is selected from the group consisting of:
CH and N;
X3 is selected from the group consisting of:
CR9 and N;
with the proviso that at least one of X2 and X3 is N;
R1 is chosen from heterocycloalkyl, which may be optionally substituted;
R2, R3, R4, and R5 are independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; and
R9 is chosen from hydrogen, alkyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
with the provisos that
when X3 is CR9; and R9 is 2-furanyl; and R1 is chosen from piperazin-1-yl and 4-(2-hydroxyethyl)piperazin-1-yl; then R2, R3, R4, and R5 are not all hydrogen; and
when X3 is N; then R1 is chosen from 4-methylpiperazin-1-yl, piperazin-1-yl, and 4-(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl); and
when compounds have structural Formula (Ma), wherein:
p is an integer from 0 to 3; and
R18 is chosen from hydrogen and methyl; and
R20 is chosen from hydrogen and chlorine; and
R19 is independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; then R19 are not all hydrogen; and
when compounds have structural Formula (Ma), wherein:
p is an integer from 0 to 3; and
R18 is methyl;
R20 is nitro;
R19 is independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; then R19 are not all hydrogen; and
R26 is chosen from hydrogen and lower alkyl; and
when compounds have structural Formula (IIIb), wherein:
q is an integer from 0 to 3; and
R21 is methyl; and
R23 is chosen from hydrogen and methyl; and
R22 is independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; then R22 are not all hydrogen; and
when compounds have structural Formula (IIIb), wherein:
R21 and R23 are hydrogen; and
R22 is independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; then R22 are not all hydrogen.
In certain embodiments provided herein,
X2 is CH;
X3 is N; and
R1 is chosen from 4-methylpiperazin-1-yl and piperazin-1-yl.
In certain embodiments provided herein,
X2 is N;
X3 is CR9; and
R9 is chosen from hydrogen, lower alkyl, halogen, haloalkyl, perhaloalkyl, amino, carboxyl, cyano, nitro, aryl, cycloalkyl, heterocycloalkyl, any of which may be optionally substituted.
In other embodiments provided herein,
X2 and X3 are N;
R1 is chosen from 4-methylpiperazin-1-yl and piperazin-1-yl; and
R4 is chosen from cyano, halogen, haloalkyl, perhaloalkyl, and perhaloalkoxy.
Provided herein are compounds of structural Formula (IV), or a salt thereof, wherein,
or a salt, wherein:
the 5-membered ring comprising X2, X3, and X5 is aromatic;
X5 is chosen from C and N;
X2 is selected from the group consisting of:
N, when X5 is N; and
O and CR6, when X5 is C;
X3 is chosen from CR9 and O, when X5 is C; and
CR9, when X5 is N;
R1 is heterocycloalkyl, which may be optionally substituted;
R2, R3, R4, and R5 are independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; and
R6 and R9 are independently chosen from hydrogen, alkyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
with the provisos that
when X5 is N; then R1 is chosen from 4-methylpiperazin-1-yl, piperazin-1-yl and bicyclic heterocycloalkyl;
when X2 is O; and X3 is CR9; and X5 is C; then R1 cannot be 4-morpholino, 4-piperidinyl, or 4-phenylpiperidin-4-ol;
when X2 is N; and X3 is CR9; and X5 is N; and R1 is 4-methylpiperazin-1-yl; and R4 is hydrogen; then R2, R3, R5, and R9 are not all hydrogen; and
when X2 is N; and X3 is CR9; and X5 is N; and R1 is piperazin-1-yl; and R4 is methyl; then R2, R3, R5, and R9 are not all hydrogen; and
when X2 is N; and X3 is CR9; and X5 is N; and R1 is 4-methylpiperazin-1-yl; and R4 is methoxy; then R3 cannot be methoxy.
In certain embodiments provided herein, X5 is N.
In other embodiments provided herein,
X2 is N;
X3 is CR9;
R4 is chosen from halogen, haloalkyl, lower alkenyl, perhaloalkyl, and perhaloalkoxy; and
R9 is chosen from hydrogen and lower alkyl.
In further embodiments provided herein, X5 is C.
In yet further embodiments provided herein,
X2 is CR6; and
X3 is O.
In certain embodiments provided herein,
X2 is O;
X3 is CR9; and
R1 is chosen from a 5-membered heterocycloalkyl and a 6-membered heterocycloalkyl containing at least two nitrogens.
In certain embodiments provided herein, compounds of Formula I have a structural formula chosen from:
wherein R28 is chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted.
In certain embodiments provided herein,
R2, R3, R4, and R5 are independently chosen from hydrogen, C1-C10 alkyl, C1-C10 alkenyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, cyano, and nitro; and
R9 is chosen from hydrogen, C1-C10 alkyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, amino, carboxyl, cyano, nitro, aryl, heteroaryl, cycloalkyl, heterocycloalkyl, any of which may be optionally substituted.
In other embodiments provided herein,
R2, R3, and R5 are independently chosen from hydrogen, cyano, lower alkyl, lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy; and
R4 is chosen from cyano, lower alkyl, lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy.
In further embodiments provided herein,
R2, R3, and R5 are independently chosen from hydrogen, cyano lower alkyl, lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy; and
R4 is chosen from lower alkyl, cyano, lower alkenyl, bromine, fluorine, perhaloalkyl, haloalkyl, and perhaloalkoxy.
In certain embodiments provided herein,
R2 is chosen from lower alkyl, lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy;
R3 and R5 are independently chosen from hydrogen, lower alkyl, lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy; and
R4 is chosen from lower alkyl, cyano, lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy.
In certain embodiments provided herein,
R2 and R5 are independently chosen from hydrogen, lower alkyl, lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy;
R3 is chosen from lower alkyl, lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy; and
R4 is chosen from lower alkyl, cyano lower alkenyl, halogen, perhaloalkyl, haloalkyl, and perhaloalkoxy.
In other embodiments provided herein, R2, R3, R4, and R5 are independently chosen from hydrogen, cyano, lower alkyl, halogen, haloalkyl, perhaloalkyl, and perhaloalkoxy.
In further embodiments provided herein, R2, R3, and R5 are independently chosen from hydrogen, halogen, haloalkyl, lower alkyl, lower alkenyl, alkoxy, perhaloalkyl, and perhaloalkoxy.
In yet further embodiments provided herein, R2, R3 and R5 are independently chosen from hydrogen, halogen, haloalkyl, lower alkyl, perhaloalkyl, and perhaloalkoxy.
In other embodiments provided herein, R4 is chosen from cyano, halogen, lower alkyl, lower alkenyl, perhaloalkoxy, and perhaloalkyl.
In certain embodiments provided herein, R4 is chosen from cyano, halogen, C1-C3 alkyl, and perhaloakyl.
In certain embodiments provided herein, wherein R4 is chosen from cyano, methyl, halogen, and perhaloalkyl.
In other embodiments provided herein, wherein R4 is chosen from cyano, methyl, bromine, chlorine, and perhaloalkyl
In further embodiments provided herein, R4 is chosen from cyano, halogen, and perhaloalkyl.
In yet further embodiments provided herein, R4 is chosen from cyano, bromine, chlorine, and perhaloalkyl.
In certain embodiments provided herein, R4 is perhaloalkyl.
In other embodiments provided herein, R4 is halogen.
In other embodiments provided herein, R4 is cyano.
In other embodiments provided herein, R3 and R4 are halogen.
In further embodiments provided herein, R2 and R3 are independently chosen from hydrogen and halogen.
In yet further embodiments provided herein, R2 and R3 are independently chosen from hydrogen, chlorine, and fluorine.
In yet further embodiments provided herein, R2 and R3 are hydrogen.
In certain embodiments provided herein, R3 is chosen from hydrogen, C1-C3 alkyl, halogen, and perhaloalkyl.
In other embodiments provided herein, R3 is hydrogen.
In other embodiments provided herein, R3 is halogen.
In further embodiments provided herein, R2 and R5 are independently chosen from hydrogen, lower alkyl, halogen, and perhaloalkyl.
In certain embodiments provided herein, R2 and R5 are independently chosen from hydrogen and halogen.
In other embodiments provided herein, R5 is hydrogen.
In other embodiments provided herein, R2 is halogen.
In further embodiments provided herein, R2 is hydrogen.
In further embodiments provided herein,
R1 is piperazin-1-yl;
R2 is hydrogen; and
R4 is chosen from cyano, halogen, and perhaloalkyl.
In yet further embodiments provided herein,
R2 is hydrogen;
R3 is halogen; and
R4 is methyl.
In yet further embodiments provided herein,
R2 and R4 are halogen; and
R3 is hydrogen.
In yet further embodiments provided herein,
R2 and R3 are hydrogen; and
R4 is perhaloalkyl.
In certain embodiments provided herein, R9 is chosen from hydrogen and C1-C3 alkyl.
In other embodiments provided herein, R9 is chosen from hydrogen and methyl.
In other embodiments provided herein,
R3 is hydrogen; and
R9 is methyl.
In certain embodiments provided herein, R6 is hydrogen.
In certain embodiments, R1 is chosen from 4-methylpiperazin-1-yl and piperazin-1-yl.
In other embodiments provided herein, R1 is 4-methylpiperazin-1-yl.
In further embodiments provided herein, R1 is piperazin-1-yl.
A compound chosen from Examples 251-519, or a salt thereof.
Provided herein are compounds of structural Formula (V):
or a salt thereof, wherein:
X1 and X5 are independently chosen from C, CH and N;
X2 is chosen from [C(R6)(R7)]n, NR8, and O;
X3 is chosen from [C(R9)(R10)]m and NR11, and O;
X4 is chosen from [C(R12)(R13)] and NR14;
the ring comprising X1-X5 is aromatic and comprises at least two heteroatoms;
R1 is optionally substituted 4- to 7-membered monocyclic heterocycloalkyl;
R4 is chosen from halogen, perhalomethyl, perhalomethoxy, and cyano;
R2, R3, are independently chosen from hydrogen, halogen, perhalomethyl, perhalomethoxy, and cyano;
R6, R7, R9, R10, R12, and R13 are independently chosen from null, hydrogen, lower alkyl, heteroalkyl, lower alkoxy, halogen, lower haloalkyl, lower amino, carboxyl, hydroxy, cyano, and nitro, any of which may be optionally substituted; and
R8, R11, and R14 are independently chosen from null, hydrogen, lower alkyl, lower heteroalkyl, lower alkoxy, and lower haloalkyl, any of which may be optionally substituted;
and with the proviso that:
when X1 is C, X2 is NR8, R8 is null, X3 [C(R9)(R10)]m, m is 1, R9 is null, X4 is NR14, R14 is null, X5 is N, R1 is methylpiperazine, R4 is perfluoromethyl, and R5 is fluoro,
then R10 is hydrogen.
In certain embodiments, R6, R8, R10, and R14 are independently chosen from null and hydrogen.
A compound of structural Formula (Va):
or a salt thereof, wherein:
In certain embodiments provided herein, compounds of Formula V have a structural formula chosen from:
or a salt thereof, wherein:
In certain embodiments provided herein, compounds of Formula V have a structural formula chosen from:
or a salt thereof, wherein:
In certain embodiments, one of R3 and R4 is hydrogen.
In certain embodiments, R5 is fluoro.
In certain embodiments, R4 is chosen from bromine, chlorine, and CF3.
In certain embodiments:
R4 is chosen from bromine, chlorine, and CF3; and
R5 is fluoro.
In certain embodiments provided herein, compounds of Formula V have a structural formula chosen from:
or a salt thereof, wherein:
R1 is optionally substituted 4- to 7-membered monocyclic heterocycloalkyl;
R5 is chosen from halogen, perhalomethyl, perhalomethoxy, and cyano;
R3 and R4 are independently chosen from hydrogen, halogen, perhalomethyl, perhalomethoxy, and cyano; and
R7, R9, and R11 are independently chosen from hydrogen and lower alkyl.
In certain embodiments, one of R3 and R4 is hydrogen.
In certain embodiments, R5 is fluoro.
In certain embodiments, R4 is chosen from bromine, chlorine, and CF3.
In certain embodiments, R3 is fluoro.
In certain embodiments,
R4 is chosen from bromine, chlorine, and CF3; and
R5 is fluoro.
Provided herein are compounds of structural Formula (VI)
or a salt thereof, wherein:
Provided herein are compounds of structural Formula (VII)
or a salt thereof, wherein:
Provided herein are compounds of structural Formula (VIII)
or a salt thereof, wherein:
In certain embodiments:
X8 is CH;
m and n are each 1; and
R24 is chosen from hydrogen, amino, and lower alkyl.
In certain embodiments, R24 is lower amino.
In certain embodiments, R24 is NHCH3.
In certain embodiments:
X8 is N;
m and n are each 2; and
R24 is chosen from hydrogen and lower alkyl.
In certain embodiments, R24 is chosen from hydrogen and methyl.
In certain embodiments, R24 is methyl.
Provided herein are compounds of structural Formula (IX)
or a salt thereof, wherein:
X8 is chosen from CH and N;
p and q are each an integer chosen from 1 and 2;
R5 is chosen from halogen, perhalomethyl, perhalomethoxy, and cyano;
R3 and R4 are independently chosen from hydrogen, halogen, perhalomethyl, perhalomethoxy, and cyano;
R9 is chosen from hydrogen and lower alkyl; and
R24 is chosen from hydrogen, amino, and lower alkyl.
In certain embodiments, R9 is chosen from hydrogen and methyl.
In certain embodiments:
X8 is CH;
m and n are each 1; and
R24 is chosen from hydrogen, amino, and lower alkyl.
In certain embodiments, R24 is lower amino.
In certain embodiments, R5 is fluoro.
In certain embodiments, R4 is chosen from bromine, chlorine, and CF3.
In certain embodiments, R3 is fluoro.
In certain embodiments, R24 is NHCH3.
In certain embodiments:
X8 is N;
m and n are each 2; and
R24 is chosen from hydrogen and lower alkyl.
In certain embodiments, R5 is fluoro.
In certain embodiments, R4 is chosen from bromine, chlorine, and CF3.
In certain embodiments, R3 is fluoro.
In certain embodiments, R24 is chosen from hydrogen and methyl.
In certain embodiments, R24 is methyl.
Also provided herein is a compound of structural Formula (X):
or a salt thereof, wherein:
X1 and X5 are independently chosen from C, CH and N;
X2 is chosen from [C(R6)(R7)]1, NR8, O and S;
X3 is chosen from [C(R9)(R10)]m, NR11, O, and S;
X4 is chosen from [C(R12)(R13)], NR14, O and S;
n and m are each an integer from 1 to 2;
Y1 is chosen from a bond, lower alkyl, lower alkoxy, OR15, NR16R17, and lower aminoalkyl;
R2, R3, R4, and R5 are independently chosen from hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, perhaloalkoxy, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
R6, R7, R9, R10, R12, and R13 are independently chosen from null, hydrogen, alkyl, heteroalkyl, alkoxy, halogen, haloalkyl, perhaloalkyl, amino, aminoalkyl, amido, carboxyl, acyl, hydroxy, cyano, nitro, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
R8, R11, and R14 are independently chosen from null, hydrogen, alkyl, heteroalkyl, alkoxy, haloalkyl, perhaloalkyl, aminoalkyl, C-amido, carboxyl, acyl, hydroxy, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted;
R15 and R16 are independently chosen from aminoalkyl, alkylaminoalkyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, ether, heterocycloalkyl, lower alkylaminoheterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted; and
R17 is independently chosen from hydrogen, aminoalkyl, alkylaminoalkyl aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, ether, heterocycloalkyl, lower alkylaminoheterocycloalkyl, heterocycloalkylalkyl, heteroaryl, and heteroarylalkyl, any of which may be optionally substituted.
In certain embodiments, compounds have structural Formula (XI):
or a salt thereof, wherein:
X1 and X5 are independently chosen from C, CH and N;
X2 is chosen from [C(R6)(R7)]n, NR8, and O;
X3 is chosen from [C(R9)(R10)]m and NR11, and O;
X4 is chosen from [C(R12)(R13)] and NR14;
R1 is optionally substituted 4- to 7-membered monocyclic heterocycloalkyl;
R2, R3, R4, and R5 are independently chosen from hydrogen, halogen, perhalomethyl, perhalomethoxy, and cyano;
R6, R7, R9, R10, R12, and R13 are independently chosen from null, hydrogen, lower alkyl, heteroalkyl, lower alkoxy, halogen, lower haloalkyl, lower amino, carboxyl, hydroxy, cyano, and nitro, any of which may be optionally substituted;
R8, R11, and R14 are independently chosen from null, hydrogen, lower alkyl, lower heteroalkyl, lower alkoxy, and lower haloalkyl, any of which may be optionally substituted; and
R24 is chosen from hydrogen, lower amino, and lower alkyl;
with the proviso that
when X1 is N, X2 is [C(R6)(R7)]n, X3 is NR11, X4 is NR14, X5 is C, R2 is hydrogen, R3 is hydrogen, R5 is hydrogen, R6-R10 and R12-R14 are chosen from null and hydrogen, and R24 is NH2,
then R5 is not chlorine.
In certain embodiments are provided compounds having a structural formula chosen from:
In certain embodiments:
R7, R9, and R11 are independently chosen from null, hydrogen, and lower alkyl; and
R24 is chosen from hydrogen, lower amino, and lower alkyl.
In certain embodiments, R24 is lower amino.
In certain embodiments, R24 is NHCH3.
In certain embodiments, R3 and R5 are independently chosen from hydrogen and fluorine.
In certain embodiments, R4 is chosen from cyano, bromine, chlorine, and CF3.
In certain embodiments, R5 is fluoro.
In certain embodiments:
R2 is hydrogen; and
at least one of R3 and R5 is hydrogen.
In certain embodiments, R4 is chosen from cyano, bromine, chlorine, and CF3.
In certain embodiments, R4 is cyano.
In certain embodiments, R24 is NHCH3.
In certain embodiments, R2 is hydrogen.
In certain embodiments, R2, R3, and R5 are hydrogen.
Also provided are compounds having structural Formula (XII)
or a salt thereof, wherein:
X3 is chosen from C(R9) and N;
R2, R3, R4, and R5 are independently chosen from hydrogen, halogen, perhalomethyl, perhalomethoxy, and cyano;
R9 is chosen from hydrogen and lower alkyl; and
R24 is chosen from hydrogen, lower amino, and lower alkyl.
Also provided are compounds having structural Formula (XIII):
or a salt thereof, wherein:
In certain embodiments are provided compounds having a structural formula chosen from:
In certain embodiments are provided compounds having a structural formula chosen from:
Also provided herein is a pharmaceutical composition comprising a compound as disclosed herein, together with a pharmaceutically acceptable carrier.
In certain embodiments, the pharmaceutical composition comprises at least one compound chosen from those recited in Examples 251-415 and 417-519 or a salt thereof, together with a pharmaceutically acceptable carrier.
Also provided is a pharmaceutical composition comprising:
In certain embodiments, the other therapeutic agent is chosen from acrivastine, alcaftadine, antazoline, azelastine, bromazine, brompheniramine, cetirizine, chlorpheniramine, clemastine, desloratidine, diphenhydramine, diphenylpyraline, ebastine, emedastine, epinastine, fexofenadine, hydroxyzine, ketotifen, levocabastine, levocetirizine, loratidine, methdilazine, mizolastine, promethazine, olopatadine, triprolidine, fluticasone, budesonide, beclomethasone, mometasone and ciclesonide.
Also provided herein is a method of treatment of an H4R-mediated disease comprising the administration, to a patient in need thereof, of a therapeutically effective amount of a compound as disclosed herein.
In certain embodiments provided herein, said treatment is systemic.
In certain embodiments, said administration is topical.
In certain embodiments, said disease is chosen from an inflammatory disease, an autoimmune disease, an allergic disorder, and an ocular disorder.
In certain embodiments, disease is chosen from pruritus, eczema, atopic dermatitis, asthma, chronic obstructive pulmonary disease (COPD), allergic rhinitis, non-allergic rhinitis, rhinosinusitis, nasal inflammation, nasal congestion, sinus congestion, otic inflammation dry eye, ocular inflammation, allergic conjunctivitis, vernal conjunctivitis, vernal keratoconjunctivitis, and giant papillary conjunctivitis.
In certain embodiments, said topical administration is to the skin.
In certain embodiments, said topical administration is to the eye.
In certain embodiments, said topical administration is intranasal, otic, or by inhalation.
Also provided herein is the use of a compound as disclosed herein in the manufacture of a medicament for the treatment of an H4R-mediated disease comprising the administration of:
a therapeutically effective amount of a compound as recited herein; and
another therapeutic agent.
Also provided herein is a method for achieving an effect in a patient comprising the administration of a therapeutically effective amount of a compound as disclosed herein to a patient, wherein the effect is chosen from reduction in the number of mast cells, inhibition of eosiniphil migration optionally to the nasal mucosa, the eye, or the wound site, reduction in inflammatory markers, reduction in inflammatory cytokines, reduction in scratching, relief of symptoms and/or signs of nasal congestion from allergic and non-allergic causes, decreased watering or redness of the eyes, and reduction in ocular pain.
Also provided herein is a compound as recited herein for use as a medicament.
Also provided herein is a compound as recited herein for use in the manufacture of a medicament for the prevention or treatment of a disease or condition ameliorated by the inhibition of H1R and/or H4R.
Also provided herein is a compound as disclosed herein for use as a medicament.
Also provided herein is a compound as disclosed herein for use in the manufacture of a medicament for the prevention or treatment of a disease or condition ameliorated by the inhibition of H1R and/or H4R.
Also provided herein is use of a compound as disclosed herein in the manufacture of a medicament for the prevention or treatment of a disease or condition ameliorated by the inhibition of H4R.
In certain embodiments, the medicament is formulated for systemic administration. In other embodiments, the medicament is formulated for topical administration.
Also provided herein is use of a compound as disclosed herein in the manufacture of a combination medicament for reduction in the number of mast cells; inhibition of inflammatory cell (e.g., granulocytes including eosinophils, basophils, and neutrophils, mast cells, lymphocytes, and dendritic cells) migration to the nasal mucosa, the ear, the eye, or the wound site; reduction in inflammatory markers; reduction in inflammatory cytokines; reduction in scratching; relief of symptoms of nasal congestion from allergic or non-allergic causes; decreased watering or redness of the eyes; or reduction in ocular pain.
Also provided herein is use of a compound as disclosed herein in the manufacture of a medicament for the treatment of the pain or inflammation resulting from cataract surgery.
Also provided herein is use of a compound as disclosed herein in the manufacture of a combination medicament for the prevention or treatment of an H4R-mediated disease, together with another therapeutic agent.
Also provided herein is use of a compound as disclosed herein, together with another therapeutic agent, in the manufacture of a combination medicament for reduction in the number of mast cells; inhibition of inflammatory cell (e.g., granulocytes including eosinophils, basophils, and neutrophils, mast cells, lymphocytes, and dendritic cells) migration to the nasal mucosa, the ear, the eye, or the wound site; reduction in inflammatory markers; reduction in inflammatory cytokines; reduction in scratching; relief of symptoms of nasal congestion from allergic or non-allergic causes; decreased watering or redness of the eyes; or reduction in ocular pain.
Also provided herein is the use of a compound as disclosed herein in the inhibition of H4R comprising contacting H4R with a compound as recited herein.
In certain embodiments, the contacting causes inhibition which is competitive with histamine.
As used herein, the terms below have the meanings indicated.
When ranges of values are disclosed, and the notation “from n1 . . . to n2” is used, where n1 and n2 are the numbers, then unless otherwise specified, this notation is intended to include the numbers themselves and the range between them. This range may be integral or continuous between and including the end values. By way of example, the range “from 2 to 6 carbons” is intended to include two, three, four, five, and six carbons, since carbons come in integer units. Compare, by way of example, the range “from 1 to 3 μM (micromolar),” which is intended to include 1 μM, 3 μM, and everything in between to any number of significant figures (e.g., 1.255 μM, 2.1 μM, 2.9999 μM, etc.).
The term “about,” as used herein, is intended to qualify the numerical values which it modifies, denoting such a value as variable within a margin of error. When no particular margin of error, such as a standard deviation to a mean value given in a chart or table of data, is recited, the term “about” should be understood to mean that range which would encompass the recited value and the range which would be included by rounding up or down to that figure as well, taking into account significant figures.
The term “acyl,” as used herein, alone or in combination, refers to a carbonyl attached to an alkenyl, alkyl, aryl, cycloalkyl, heteroaryl, heterocycle, or any other moiety where the atom attached to the carbonyl is carbon. An “acetyl” group refers to a —C(O)CH3 group. An “alkylcarbonyl” or “alkanoyl” group refers to an alkyl group attached to the parent molecular moiety through a carbonyl group. Examples of such groups include methylcarbonyl and ethylcarbonyl. Examples of acyl groups include formyl, alkanoyl and aroyl.
The term “alkenyl,” as used herein, alone or in combination, refers to a straight-chain or branched-chain hydrocarbon group having one or more double bonds and containing from 2 to 20 carbon atoms. In certain embodiments, said alkenyl will comprise from 2 to 6 carbon atoms. The term “alkenylene” refers to a carbon-carbon double bond system attached at two or more positions such as ethenylene [(—CH═CH—), (—C::C—)]. Examples of suitable alkenyl groups include ethenyl, propenyl, 2-methylpropenyl, 1,4-butadienyl and the like. Unless otherwise specified, the term “alkenyl” may include “alkenylene” groups.
The term “alkoxy,” as used herein, alone or in combination, refers to an alkyl ether group, wherein the term alkyl is as defined below. Examples of suitable alkyl ether groups include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, iso-butoxy, sec-butoxy, tert-butoxy, and the like.
The term “alkyl,” as used herein, alone or in combination, refers to a straight-chain or branched-chain alkyl group containing from 1 to 20 carbon atoms. In certain embodiments, said alkyl group will comprise from 1 to 10 carbon atoms. In further embodiments, said alkyl group will comprise from 1 to 6 carbon atoms. Alkyl groups may be optionally substituted as defined herein. Examples of alkyl groups include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, octyl, noyl and the like. The term “alkylene,” as used herein, alone or in combination, refers to a saturated aliphatic group derived from a straight or branched chain saturated hydrocarbon attached at two or more positions, such as methylene (—CH2—). Unless otherwise specified, the term “alkyl” may include “alkylene” groups.
The term “alkylamino,” as used herein, alone or in combination, refers to an alkyl group attached to the parent molecular moiety through an amino group. Suitable alkylamino groups may be mono- or dialkylated, forming groups such as, for example, N-methylamino, N-ethylamino, N,N-dimethylamino, N,N-ethylmethylamino and the like.
The term “alkylidene,” as used herein, alone or in combination, refers to an alkenyl group in which one carbon atom of the carbon-carbon double bond belongs to the moiety to which the alkenyl group is attached.
The term “alkylthio,” as used herein, alone or in combination, refers to an alkyl thioether (R—S—) group wherein the term alkyl is as defined above and wherein the sulfur may be singly or doubly oxidized. Examples of suitable alkyl thioether groups include methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, iso-butylthio, sec-butylthio, tert-butylthio, methanesulfonyl, ethanesulfinyl, and the like.
The term “alkynyl,” as used herein, alone or in combination, refers to a straight-chain or branched chain hydrocarbon group having one or more triple bonds and containing from 2 to 20 carbon atoms. In certain embodiments, said alkynyl group comprises from 2 to 6 carbon atoms. In further embodiments, said alkynyl group comprises from 2 to 4 carbon atoms. The term “alkynylene” refers to a carbon-carbon triple bond attached at two positions such as ethynylene (—C:::C—, —C≡C—). Examples of alkynyl groups include ethynyl, propynyl, hydroxypropynyl, butyn-1-yl, butyn-2-yl, pentyn-1-yl, 3-methylbutyn-1-yl, hexyn-2-yl, and the like. Unless otherwise specified, the term “alkynyl” may include “alkynylene” groups.
The terms “amido” and “carbamoyl,” as used herein, alone or in combination, refer to an amino group as described below attached to the parent molecular moiety through a carbonyl group, or vice versa. The term “C-amido” as used herein, alone or in combination, refers to a —C(═O)—NR2 group with R as defined herein. The term “N-amido” as used herein, alone or in combination, refers to a RC(═O)NH— group, with R as defined herein. The term “acylamino” as used herein, alone or in combination, embraces an acyl group attached to the parent moiety through an amino group. An example of an “acylamino” group is acetylamino (CH3C(O)NH—).
The term “amino,” as used herein, alone or in combination, refers to NRR′, wherein R and R′ are independently chosen from hydrogen, alkyl, acyl, heteroalkyl, aryl, cycloalkyl, heteroaryl, and heterocycloalkyl, any of which may themselves be optionally substituted. Additionally, R and R′ may combine to form heterocycloalkyl, either of which may be optionally substituted.
The term “aryl,” as used herein, alone or in combination, means a carbocyclic aromatic system containing one, two or three rings wherein such polycyclic ring systems are fused together. The term “aryl” embraces aromatic groups such as phenyl, naphthyl, anthracenyl, and phenanthryl.
The term “arylalkenyl” or “aralkenyl,” as used herein, alone or in combination, refers to an aryl group attached to the parent molecular moiety through an alkenyl group.
The term “arylalkoxy” or “aralkoxy,” as used herein, alone or in combination, refers to an aryl group attached to the parent molecular moiety through an alkoxy group.
The term “arylalkyl” or “aralkyl,” as used herein, alone or in combination, refers to an aryl group attached to the parent molecular moiety through an alkyl group.
The term “arylalkynyl” or “aralkynyl,” as used herein, alone or in combination, refers to an aryl group attached to the parent molecular moiety through an alkynyl group.
The term “arylalkanoyl” or “aralkanoyl” or “aroyl,” as used herein, alone or in combination, refers to an acyl group derived from an aryl-substituted alkanecarboxylic acid such as benzoyl, naphthoyl, phenylacetyl, 3-phenylpropionyl (hydrocinnamoyl), 4-phenylbutyryl, (2-naphthyl)acetyl, 4-chlorohydrocinnamoyl, and the like.
The term aryloxy as used herein, alone or in combination, refers to an aryl group attached to the parent molecular moiety through an oxy.
The terms “benzo” and “benz,” as used herein, alone or in combination, refer to the divalent group C6H4=derived from benzene. Examples include benzothiophene and benzimidazole.
The term “carbamate,” as used herein, alone or in combination, refers to an ester of carbamic acid (—NHCOO—) which may be attached to the parent molecular moiety from either the nitrogen or acid end, and which may be optionally substituted as defined herein.
The term “O-carbamyl” as used herein, alone or in combination, refers to a —OC(O)NRR′ group, with R and R′ as defined herein.
The term “N-carbamyl” as used herein, alone or in combination, refers to a ROC(O)NR′— group, with R and R′ as defined herein.
The term “carbonyl,” as used herein, when alone includes formyl [—C(O)H] and in combination is a —C(O)— group.
The term “carboxyl” or “carboxy,” as used herein, refers to —C(O)OH or the corresponding “carboxylate” anion, such as is in a carboxylic acid salt. An “O-carboxy”group refers to a RC(O)O— group, where R is as defined herein. A “C-carboxy” group refers to a —C(O)OR groups where R is as defined herein.
The term “cyano,” as used herein, alone or in combination, refers to —CN.
The term “cycloalkyl,” or, alternatively, “carbocycle,” as used herein, alone or in combination, refers to a saturated or partially saturated monocyclic, bicyclic or tricyclic alkyl group wherein each cyclic moiety contains from 3 to 12 carbon atom ring members and which may optionally be a benzo fused ring system which is optionally substituted as defined herein. In certain embodiments, said cycloalkyl will comprise from 5 to 7 carbon atoms. Examples of such cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, tetrahydronaphthyl, indanyl, octahydronaphthyl, 2,3-dihydro-1H-indenyl, adamantyl and the like. “Bicyclic” and “tricyclic” as used herein are intended to include both fused ring systems, such as decahydronaphthalene, octahydronaphthalene as well as the multicyclic (multicentered) saturated or partially unsaturated type. The latter type of isomer is exemplified in general by bicyclo[1,1,1]pentane, camphor, adamantane, and bicyclo[3,2,1]octane.
The term “ester,” as used herein, alone or in combination, refers to a carboxy group bridging two moieties linked at carbon atoms.
The term “ether,” as used herein, alone or in combination, refers to an oxy group bridging two moieties linked at carbon atoms.
The term “halo,” or “halogen,” as used herein, alone or in combination, refers to fluorine, chlorine, bromine, or iodine.
The term “haloalkoxy,” as used herein, alone or in combination, refers to a haloalkyl group attached to the parent molecular moiety through an oxygen atom.
The term “haloalkyl,” as used herein, alone or in combination, refers to an alkyl group having the meaning as defined above wherein one or more hydrogens are replaced with a halogen. Specifically embraced are monohaloalkyl, dihaloalkyl and polyhaloalkyl groups. A monohaloalkyl group, for one example, may have an iodo, bromo, chloro or fluoro atom within the group. Dihalo and polyhaloalkyl groups may have two or more of the same halo atoms or a combination of different halo groups. Examples of haloalkyl groups include fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, pentafluoroethyl, heptafluoropropyl, difluorochloromethyl, dichlorofluoromethyl, difluoroethyl, difluoropropyl, dichloroethyl and dichloropropyl. “Haloalkylene” refers to a haloalkyl group attached at two or more positions. Examples include fluoromethylene (—CFH—), difluoromethylene (—CF2—), chloromethylene (—CHCl—) and the like.
The term “heteroalkyl,” as used herein, alone or in combination, refers to a stable straight or branched chain, or cyclic hydrocarbon group, or combinations thereof, fully saturated or containing from 1 to 3 degrees of unsaturation, consisting of the stated number of carbon atoms and from one to three heteroatoms chosen from O, N, and S, and wherein the nitrogen and sulfur atoms may optionally be oxidized and the nitrogen heteroatom may optionally be quaternized. The heteroatom(s) O, N and S may be placed at any interior position of the heteroalkyl group. Up to two heteroatoms may be consecutive, such as, for example, —CH2—NH—OCH3.
The term “heteroaryl,” as used herein, alone or in combination, refers to a 3 to 7 membered unsaturated heteromonocyclic ring, or a fused monocyclic, bicyclic, or tricyclic ring system in which at least one of the fused rings is aromatic, which contains at least one atom chosen from O, S, and N. In certain embodiments, said heteroaryl will comprise from 5 to 7 carbon atoms. The term also embraces fused polycyclic groups wherein heterocyclic rings are fused with aryl rings, wherein heteroaryl rings are fused with other heteroaryl rings, wherein heteroaryl rings are fused with heterocycloalkyl rings, or wherein heteroaryl rings are fused with cycloalkyl rings. Examples of heteroaryl groups include pyrrolyl, pyrrolinyl, imidazolyl, pyrazolyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazolyl, pyranyl, furyl, thienyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, thiadiazolyl, isothiazolyl, indolyl, isoindolyl, indolizinyl, benzimidazolyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolinyl, indazolyl, benzotriazolyl, benzodioxolyl, benzopyranyl, benzoxazolyl, benzoxadiazolyl, benzothiazolyl, benzothiadiazolyl, benzofuryl, benzothienyl, chromonyl, coumarinyl, benzopyranyl, tetrahydroquinolinyl, tetrazolopyridazinyl, tetrahydroisoquinolinyl, thienopyridinyl, furopyridinyl, pyrrolopyridinyl and the like. Exemplary tricyclic heterocyclic groups include carbazolyl, benzidolyl, phenanthrolinyl, dibenzofuranyl, acridinyl, phenanthridinyl, xanthenyl and the like.
The terms “heterocycloalkyl” and, interchangeably, “heterocycle,” as used herein, alone or in combination, each refer to a saturated, partially unsaturated, or fully unsaturated monocyclic, bicyclic, or tricyclic heterocyclic group containing at least one heteroatom as a ring member, wherein each said heteroatom may be independently chosen from nitrogen, oxygen, and sulfur. In certain embodiments, said heterocycloalkyl will comprise from 1 to 4 heteroatoms as ring members. In further embodiments, said heterocycloalkyl will comprise from 1 to 2 heteroatoms as ring members. In certain embodiments, said heterocycloalkyl will comprise from 3 to 8 ring members in each ring. In further embodiments, said heterocycloalkyl will comprise from 3 to 7 ring members in each ring. In yet further embodiments, said heterocycloalkyl will comprise from 5 to 6 ring members in each ring. “Heterocycloalkyl” and “heterocycle” are intended to include sulfones, sulfoxides, N-oxides of tertiary nitrogen ring members, and carbocyclic fused and benzo fused ring systems; additionally, both terms also include systems where a heterocycle ring is fused to an aryl group, as defined herein, or an additional heterocycle group. Examples of heterocycle groups include aziridinyl, azetidinyl, 1,3-benzodioxolyl, dihydroisoindolyl, dihydroisoquinolinyl, dihydrocinnolinyl, dihydrobenzodioxinyl, dihydro[1,3]oxazolo[4,5-b]pyridinyl, benzothiazolyl, dihydroindolyl, dihy-dropyridinyl, 1,3-dioxanyl, 1,4-dioxanyl, 1,3-dioxolanyl, isoindolinyl, morpholinyl, piperazinyl, pyrrolidinyl, tetrahydropyridinyl, piperidinyl, thiomorpholinyl, and the like. The heterocycle groups may be optionally substituted unless specifically prohibited.
The term “hydrazinyl” as used herein, alone or in combination, refers to two amino groups joined by a single bond, i.e., —N—N—.
The term “hydroxy,” as used herein, alone or in combination, refers to —OH.
The term “hydroxyalkyl,” as used herein, alone or in combination, refers to a hydroxy group attached to the parent molecular moiety through an alkyl group.
The term “imino,” as used herein, alone or in combination, refers to ═N—.
The term “iminohydroxy,” as used herein, alone or in combination, refers to ═N(OH) and ═N—O—.
The phrase “in the main chain” refers to the longest contiguous or adjacent chain of carbon atoms starting at the point of attachment of a group to the compounds of any one of the formulas disclosed herein.
The term “isocyanato” refers to a —NCO group.
The term “isothiocyanato” refers to a —NCS group.
The phrase “linear chain of atoms” refers to the longest straight chain of atoms independently selected from carbon, nitrogen, oxygen and sulfur.
The term “lower,” as used herein, alone or in a combination, where not otherwise specifically defined, means containing from 1 to and including 6 carbon atoms.
The term “lower aryl,” as used herein, alone or in combination, means phenyl or naphthyl, which may be optionally substituted as provided.
The term “lower heteroalkyl,” as used herein, alone or in combination, refers to a stable straight or branched chain, or cyclic hydrocarbon group, or combinations thereof, fully saturated or containing from 1 to 3 degrees of unsaturation, consisting of one to six atoms in which one to three may be heteroatoms chosen from O, N, and S, and the remaining atoms are carbon. The nitrogen and sulfur atoms may optionally be oxidized and the nitrogen heteroatom may optionally be quaternized. The heteroatom(s) O, N and S may be placed at any interior or terminal position of the heteroalkyl group. Up to two heteroatoms may be consecutive, such as, for example, —CH2—NH—OCH3.
The term “lower heteroaryl,” as used herein, alone or in combination, means either 1) monocyclic heteroaryl comprising five or six ring members, of which between one and four said members may be heteroatoms chosen from O, S, and N, or 2) bicyclic heteroaryl, wherein each of the fused rings comprises five or six ring members, comprising between them one to four heteroatoms chosen from O, S, and N.
The term “lower cycloalkyl,” as used herein, alone or in combination, means a monocyclic cycloalkyl having between three and six ring members. Lower cycloalkyls may be unsaturated. Examples of lower cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
The term “lower heterocycloalkyl,” as used herein, alone or in combination, means a monocyclic heterocycloalkyl having between three and six ring members, of which between one and four may be heteroatoms chosen from O, S, and N. Examples of lower heterocycloalkyls include pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl, piperazinyl, and morpholinyl. Lower heterocycloalkyls may be unsaturated.
The term “lower amino,” as used herein, alone or in combination, refers to —NRR′, wherein R and R′ are independently chosen from hydrogen, lower alkyl, and lower heteroalkyl, any of which may be optionally substituted. Additionally, the R and R′ of a lower amino group may combine to form a five- or six-membered heterocycloalkyl, either of which may be optionally substituted.
The term “mercaptyl” as used herein, alone or in combination, refers to an RS— group, where R is as defined herein.
The term “nitro,” as used herein, alone or in combination, refers to —NO2.
The terms “oxy” or “oxa,” as used herein, alone or in combination, refer to —O—.
The term “oxo,” as used herein, alone or in combination, refers to ═O.
The term “perhaloalkoxy” refers to an alkoxy group where all of the hydrogen atoms are replaced by halogen atoms.
The term “perhaloalkyl” as used herein, alone or in combination, refers to an alkyl group where all of the hydrogen atoms are replaced by halogen atoms.
The terms “sulfonate,” “sulfonic acid,” and “sulfonic,” as used herein, alone or in combination, refer to the —SO3H group and its anion as the sulfonic acid is used in salt formation.
The term “sulfanyl,” as used herein, alone or in combination, refers to —S—.
The term “sulfinyl,” as used herein, alone or in combination, refers to —S(O)—.
The term “sulfonyl,” as used herein, alone or in combination, refers to —S(O)2—.
The term “N-sulfonamido” refers to a RS(═O)2NR′— group with R and R′ as defined herein.
The term “S-sulfonamido” refers to a —S(═O)2NRR′, group, with R and R′ as defined herein.
The terms “thia” and “thio,” as used herein, alone or in combination, refer to a —S— group or an ether wherein the oxygen is replaced with sulfur. The oxidized derivatives of the thio group, namely sulfinyl and sulfonyl, are included in the definition of thia and thio.
The term “thiol,” as used herein, alone or in combination, refers to an —SH group.
The term “thiocarbonyl,” as used herein, when alone includes thioformyl —C(S)H and in combination is a —C(S)— group.
The term “N-thiocarbamyl” refers to an ROC(S)NR′— group, with R and R′ as defined herein.
The term “O-thiocarbamyl” refers to a —OC(S)NRR′ group with R and R′ as defined herein.
The term “thiocyanato” refers to a —CNS group.
Any definition herein may be used in combination with any other definition to describe a composite structural group. By convention, the trailing element of any such definition is that which attaches to the parent moiety. For example, the composite group alkylamido would represent an alkyl group attached to the parent molecule through an amido group, and the term alkoxyalkyl would represent an alkoxy group attached to the parent molecule through an alkyl group.
When a group is defined to be “null,” what is meant is that said group is absent.
The term “optionally substituted” means the anteceding group may be substituted or unsubstituted. When substituted, the substituents of an “optionally substituted” group may include, without limitation, one or more substituents independently selected from the following groups or a particular designated set of groups, alone or in combination: lower alkyl, lower alkenyl, lower alkynyl, lower alkanoyl, lower heteroalkyl, lower heterocycloalkyl, lower haloalkyl, lower haloalkenyl, lower haloalkynyl, lower perhaloalkyl, lower perhaloalkoxy, lower cycloalkyl, phenyl, aryl, aryloxy, lower alkoxy, lower haloalkoxy, oxo, lower acyloxy, carbonyl, carboxyl, lower alkylcarbonyl, lower carboxyester, lower carboxamido, cyano, hydrogen, halogen, hydroxy, amino, lower alkylamino, arylamino, amido, nitro, thiol, lower alkylthio, lower haloalkylthio, lower perhaloalkylthio, arylthio, sulfonate, sulfonic acid, trisubstituted silyl, N3, SH, SCH3, C(O)CH3, CO2CH3, CO2H, pyridinyl, thiophene, furanyl, lower carbamate, and lower urea. Two substituents may be joined together to form a fused five-, six-, or seven-membered carbocyclic or heterocyclic ring consisting of zero to three heteroatoms, for example forming methylenedioxy or ethylenedioxy. An optionally substituted group may be unsubstituted (e.g., —CH2CH3), fully substituted (e.g., —CF2CF3), monosubstituted (e.g., —CH2CH2F) or substituted at a level anywhere in-between fully substituted and monosubstituted (e.g., —CH2CF3). Where substituents are recited without qualification as to substitution, both substituted and unsubstituted forms are encompassed. Where a substituent is qualified as “substituted,” the substituted form is specifically intended. Additionally, different sets of optional substituents to a particular moiety may be defined as needed; in these cases, the optional substitution will be as defined, often immediately following the phrase, “optionally substituted with.”
The term R or the term R′, appearing by itself and without a number designation, unless otherwise defined, refers to a moiety chosen from hydrogen, alkyl, cycloalkyl, heteroalkyl, aryl, heteroaryl and heterocycloalkyl, any of which may be optionally substituted. Such R and R′ groups should be understood to be optionally substituted as defined herein. Whether an R group has a number designation or not, every R group, including R, R′ and Rn where n=(1, 2, 3, . . . n), every substituent, and every term should be understood to be independent of every other in terms of selection from a group. Should any variable, substituent, or term (e.g. aryl, heterocycle, R, etc.) occur more than one time in a formula or generic structure, its definition at each occurrence is independent of the definition at every other occurrence. Those of skill in the art will further recognize that certain groups may be attached to a parent molecule or may occupy a position in a chain of elements from either end as written. Thus, by way of example only, an unsymmetrical group such as —C(O)N(R)— may be attached to the parent moiety at either the carbon or the nitrogen.
Asymmetric centers exist in the compounds disclosed herein. These centers are designated by the symbols “R” or “S,” depending on the configuration of substituents around the chiral carbon atom. It should be understood that the invention encompasses all stereochemical isomeric forms, including diastereomeric, enantiomeric, and epimeric forms, as well as d-isomers and 1-isomers, and mixtures thereof. Individual stereoisomers of compounds can be prepared synthetically from commercially available starting materials which contain chiral centers or by preparation of mixtures of enantiomeric products followed by separation such as conversion to a mixture of diastereomers followed by separation or recrystallization, chromatographic techniques, direct separation of enantiomers on chiral chromatographic columns, or any other appropriate method known in the art. Starting compounds of particular stereochemistry are either commercially available or can be made and resolved by techniques known in the art. Additionally, the compounds disclosed herein may exist as geometric isomers. The present invention includes all cis, trans, syn, anti, entgegen (E), and zusammen (Z) isomers as well as the appropriate mixtures thereof. Additionally, compounds may exist as tautomers; all tautomeric isomers are provided by this invention. Additionally, the compounds disclosed herein can exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like. In general, the solvated forms are considered equivalent to the unsolvated forms.
The term “bond” refers to a covalent linkage between two atoms, or two moieties when the atoms joined by the bond are considered to be part of larger substructure. A bond may be single, double, or triple unless otherwise specified. A dashed line between two atoms in a drawing of a molecule indicates that an additional bond may be present or absent at that position.
The term “disease” as used herein is intended to be generally synonymous, and is used interchangeably with, the terms “disorder” and “condition” (as in medical condition), in that all reflect an abnormal condition of the human or animal body or of one of its parts that impairs normal functioning, is typically manifested by distinguishing signs and symptoms, and causes the human or animal to have a reduced duration or quality of life.
The term “combination therapy” means the administration of two or more therapeutic agents to treat a therapeutic condition or disorder described in the present disclosure. Such administration encompasses co-administration of these therapeutic agents in a substantially simultaneous manner, such as in a single capsule having a fixed ratio of active ingredients or in multiple, separate capsules for each active ingredient. In addition, such administration also encompasses use of each type of therapeutic agent in a sequential manner. In either case, the treatment regimen will provide beneficial effects of the drug combination in treating the conditions or disorders described herein.
The term “inhibition” (and by extension, “inhibitor”) as used herein encompasses all forms of functional protein (enzyme, kinase, receptor, channel, etc., for example) inhibition, including neutral antagonism, inverse agonism, competitive inhibition, and non-competitive inhibition (such as allosteric inhibition). Inhibition may be phrased in terms of an IC50, defined below. Compounds disclosed herein may be allosteric antagonists. Additionally, compounds disclosed herein may be agonists in one species and antagonists in another. Methods are known in the art, and are disclosed herein and can be adapted by those of skill in the art, to ascertain whether a compound is, for example, a suitable H4R antagonist in a species of interest.
In certain embodiments, “H1R inhibitor” is used herein to refer to a compound that exhibits an IC50 with respect to the histamine type-1 receptor of no more than about 100 μM and more typically not more than about 50 μM, as measured in the in vitro histamine receptor cell-based assays described generally hereinbelow. Similarly, “H3R inhibitor” is used herein to refer to a compound that exhibits an IC50 with respect to the histamine type-3 receptor of no more than about 100 μM and more typically not more than about 50 μM, as measured in the in vitro histamine receptor cell-based assays described generally hereinbelow. Also similarly, “H4R inhibitor” is used herein to refer to a compound that exhibits an IC50 with respect to the histamine type-4 receptor of no more than about 100 μM and more typically not more than about 50 μM, as measured in the in vitro histamine receptor cell-based assays described generally hereinbelow. In either of these scenarios, the term “EC50” may also be used. In vitro or in vivo, “EC50” refers to the concentration of a compound required to achieve half of the maximal effect in an assay or protocol, typically as compared to a reference standard. A “H1/H4 inhibitor” is used herein to refer to a compound that exhibits an IC50 with respect to both the histamine type-1 receptor and the histamine type-4 receptor of no more than about 100 μM and more typically not more than about 50 μM, as measured in the in vitro histamine receptor cell-based assays described generally hereinbelow; the amount of inhibition need not be equivalent at each receptor, but should not be negligible. In certain embodiments, such as, for example, in the case of an in vitro ligand-binding assay protocol, “IC50” is that concentration of inhibitor which is required to displace a natural ligand or reference standard to a half-maximal level. In other embodiments, such as, for example, in the case of certain cellular or in vivo protocols which have a functional readout, “IC50” is that concentration of inhibitor which reduces the activity of a functional protein (e.g., H1R and/or H4R) to a half-maximal level. Certain compounds disclosed herein have been discovered to exhibit inhibitory activity against H1R and/or H4R. In certain embodiments, compounds will exhibit an IC50 with respect to H1R and/or H4R of no more than about 10 μM; in further embodiments, compounds will exhibit an IC50 with respect to H1R and/or H4R of no more than about 5 μM; in yet further embodiments, compounds will exhibit an IC50 with respect to H1R and/or H4R of not more than about 1 μM; in yet further embodiments, compounds will exhibit an IC50 with respect to H1R and/or H4R of not more than about 200 nM, as measured in the H1R and/or H4R assay described herein.
The phrase “therapeutically effective” is intended to qualify the amount of active ingredients used in the treatment of a disease or disorder. This amount will achieve the goal of reducing or eliminating the said disease or disorder.
The term “therapeutically acceptable” refers to those compounds (or salts, prodrugs, tautomers, zwitterionic forms, etc.) which are suitable for use in contact with the tissues of patients without undue toxicity, irritation, and allergic response, are commensurate with a reasonable benefit/risk ratio, and are effective for their intended use.
As used herein, reference to “treatment” of a patient is intended to include prophylaxis. The term “patient” means all mammals including humans. Examples of patients include humans, cows, dogs, cats, goats, sheep, pigs, and rabbits. Preferably, the patient is a human.
The term “prodrug” refers to a compound that is made more active in vivo. Certain compounds disclosed herein may also exist as prodrugs, as described in Hydrolysis in Drug and Prodrug Metabolism: Chemistry, Biochemistry, and Enzymology (Testa, Bernard and Mayer, Joachim M. Wiley-VHCA, Zurich, Switzerland 2003). Prodrugs of the compounds described herein are structurally modified forms of the compound that readily undergo chemical changes under physiological conditions to provide the compound. Additionally, prodrugs can be converted to the compound by chemical or biochemical methods in an ex vivo environment. For example, prodrugs can be slowly converted to a compound when placed in a transdermal patch reservoir with a suitable enzyme or chemical reagent. Prodrugs are often useful because, in some situations, they may be easier to administer than the compound, or parent drug. They may, for instance, be bioavailable by oral administration whereas the parent drug is not. The prodrug may also have improved solubility in pharmaceutical compositions over the parent drug. A wide variety of prodrug derivatives are known in the art, such as those that rely on hydrolytic cleavage or oxidative activation of the prodrug. An example, without limitation, of a prodrug would be a compound which is administered as an ester (the “prodrug”), but then is metabolically hydrolyzed to the carboxylic acid, the active entity. Additional examples include peptidyl derivatives of a compound.
The compounds disclosed herein can exist as therapeutically acceptable salts. The present invention includes compounds listed above in the form of salts, including acid addition salts. Suitable salts include those formed with both organic and inorganic acids. Such acid addition salts will normally be pharmaceutically acceptable. However, salts of non-pharmaceutically acceptable salts may be of utility in the preparation and purification of the compound in question. Basic addition salts may also be formed and be pharmaceutically acceptable. For a more complete discussion of the preparation and selection of salts, refer to Pharmaceutical Salts: Properties, Selection, and Use (Stahl, P. Heinrich. Wiley-VCHA, Zurich, Switzerland, 2002).
The term “therapeutically acceptable salt,” as used herein, represents salts or zwitterionic forms of the compounds disclosed herein which are water or oil-soluble or dispersible and therapeutically acceptable as defined herein. The salts can be prepared during the final isolation and purification of the compounds or separately by reacting the appropriate compound in the form of the free base with a suitable acid. Representative acid addition salts include acetate, adipate, alginate, L-ascorbate, aspartate, benzoate, benzenesulfonate (besylate), bisulfate, butyrate, camphorate, camphorsulfonate, citrate, digluconate, formate, fumarate, gentisate, glutarate, glycerophosphate, glycolate, hemisulfate, heptanoate, hexanoate, hippurate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethansulfonate (isethionate), lactate, maleate, malonate, DL-mandelate, mesitylenesulfonate, methanesulfonate, naphthylenesulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, pamoate, pectinate, persulfate, 3-phenylproprionate, phosphonate, picrate, pivalate, propionate, pyroglutamate, succinate, sulfonate, tartrate, L-tartrate, trichloroacetate, trifluoroacetate, phosphate, glutamate, bicarbonate, para-toluenesulfonate (p-tosylate), and undecanoate. Also, basic groups in the compounds disclosed herein can be quaternized with methyl, ethyl, propyl, and butyl chlorides, bromides, and iodides; dimethyl, diethyl, dibutyl, and diamyl sulfates; decyl, lauryl, myristyl, and steryl chlorides, bromides, and iodides; and benzyl and phenethyl bromides. Examples of acids which can be employed to form therapeutically acceptable addition salts include inorganic acids such as hydrochloric, hydrobromic, sulfuric, and phosphoric, and organic acids such as oxalic, maleic, succinic, and citric. Salts can also be formed by coordination of the compounds with an alkali metal or alkaline earth ion. Hence, the present invention contemplates sodium, potassium, magnesium, and calcium salts of the compounds disclosed herein, and the like.
Basic addition salts can be prepared during the final isolation and purification of the compounds by reacting a carboxy group with a suitable base such as the hydroxide, carbonate, or bicarbonate of a metal cation or with ammonia or an organic primary, secondary, or tertiary amine. The cations of therapeutically acceptable salts include lithium, sodium, potassium, calcium, magnesium, and aluminum, as well as nontoxic quaternary amine cations such as ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, diethylamine, ethylamine, tributylamine, pyridine, N,N-dimethylaniline, N-methylpiperidine, N-methylmorpholine, dicyclohexylamine, procaine, dibenzylamine, N,N-dibenzylphenethylamine, 1-ephenamine, and N,N-dibenzylethylenediamine. Other representative organic amines useful for the formation of base addition salts include ethylenediamine, ethanolamine, diethanolamine, piperidine, and piperazine.
While it may be possible for the compounds of the subject invention to be administered as the raw chemical, it is also possible to present them as a pharmaceutical formulation. Accordingly, provided herein are pharmaceutical formulations which comprise one or more of certain compounds disclosed herein, or one or more pharmaceutically acceptable salts, esters, prodrugs, amides, or solvates thereof, together with one or more pharmaceutically acceptable carriers thereof and optionally one or more other therapeutic ingredients. The carrier(s) must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof. Proper formulation is dependent upon the route of administration chosen. Any of the well-known techniques, carriers, and excipients may be used as suitable and as understood in the art; e.g., in Remington's Pharmaceutical Sciences. The pharmaceutical compositions disclosed herein may be manufactured in any manner known in the art, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or compression processes.
The formulations include those suitable for oral, parenteral (including subcutaneous, intradermal, intramuscular, intravenous, intraarticular, and intramedullary), intraperitoneal, transmucosal, transdermal, rectal and topical (including dermal, buccal, sublingual, ocular, intranasal and intraocular) administration although the most suitable route may depend upon for example the condition and disorder of the recipient. The formulations may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. Typically, these methods include the step of bringing into association a compound of the subject invention or a pharmaceutically acceptable salt, ester, amide, prodrug or solvate thereof (“active ingredient”) with the carrier which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association the active ingredient with liquid carriers or finely divided solid carriers or both and then, if necessary, shaping the product into the desired formulation.
Formulations of the compounds disclosed herein suitable for oral administration may be presented as discrete units such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient; as a powder or granules; as a solution or a suspension in an aqueous liquid or a non-aqueous liquid; or as an oil-in-water liquid emulsion or a water-in-oil liquid emulsion. The active ingredient may also be presented as a bolus, electuary or paste.
Pharmaceutical preparations which can be used orally include tablets, push-fit capsules made of gelatin, as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol. Tablets may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared by compressing in a suitable machine the active ingredient in a free-flowing form such as a powder or granules, optionally mixed with binders, inert diluents, or lubricating, surface active or dispersing agents. Molded tablets may be made by molding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent. The tablets may optionally be coated or scored and may be formulated so as to provide slow or controlled release of the active ingredient therein. All formulations for oral administration should be in dosages suitable for such administration. The push-fit capsules can contain the active ingredients in admixture with filler such as lactose, binders such as starches, and/or lubricants such as talc or magnesium stearate and, optionally, stabilizers. In soft capsules, the active compounds may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols. In addition, stabilizers may be added. Dragee cores are provided with suitable coatings. For this purpose, concentrated sugar solutions may be used, which may optionally contain gum arabic, talc, polyvinyl pyrrolidone, carbopol gel, polyethylene glycol, and/or titanium dioxide, lacquer solutions, and suitable organic solvents or solvent mixtures. Dyestuffs or pigments may be added to the tablets or dragee coatings for identification or to characterize different combinations of active compound doses.
Examples of fillers or diluents for use in oral pharmaceutical formulations such as capsules and tablets include, without limitation, lactose, mannitol, xylitol, dextrose, sucrose, sorbitol, compressible sugar, microcrystalline cellulose (MCC), powdered cellulose, cornstarch, pregelatinized starch, dextrates, dextran, dextrin, dextrose, maltodextrin, calcium carbonate, dibasic calcium phosphate, tribasic calcium phosphate, calcium sulfate, magnesium carbonate, magnesium oxide, poloxamers such as polyethylene oxide, and hydroxypropyl methyl cellulose. Fillers may have complexed solvent molecules, such as in the case where the lactose used is lactose monohydrate. Fillers may also be proprietary, such in the case of the filler PROSOLV® (available from JRS Pharma). PROSOLV is a proprietary, optionally high-density, silicified microcrystalline cellulose composed of 98% microcrystalline cellulose and 2% colloidal silicon dioxide. Silicification of the microcrystalline cellulose is achieved by a patented process, resulting in an intimate association between the colloidal silicon dioxide and microcrystalline cellulose. ProSolv comes in different grades based on particle size, and is a white or almost white, fine or granular powder, practically insoluble in water, acetone, ethanol, toluene and dilute acids and in a 50 g/l solution of sodium hydroxide.
Examples of disintegrants for use in oral pharmaceutical formulations such as capsules and tablets include, without limitation, sodium starch glycolate, sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, croscarmellose sodium, povidone, crospovidone (polyvinylpolypyrrolidone), methyl cellulose, microcrystalline cellulose, powdered cellulose, low-substituted hydroxy propyl cellulose, starch, pregelatinized starch, and sodium alginate.
Additionally, glidants and lubricants may be used in oral pharmaceutical formulations to ensure an even blend of excipients upon mixing. Examples of lubricants include, without limitation, calcium stearate, glyceryl monostearate, glyceryl palmitostearate, hydrogenated vegetable oil, light mineral oil, magnesium stearate, mineral oil, polyethylene glycol, sodium benzoate, sodium lauryl sulfate, sodium stearyl fumarate, stearic acid, talc, and zinc stearate. Examples of glidants include, without limitation, silicon dioxide (SiO2), talc cornstarch, and poloxamers. Poloxamers (or LUTROL®, available from the BASF Corporation) are A-B-A block copolymers in which the A segment is a hydrophilic polyethylene glycol homopolymer and the B segment is hydrophobic polypropylene glycol homopolymer.
Examples of tablet binders include, without limitation, acacia, alginic acid, carbomer, carboxymethyl cellulose sodium, dextrin, ethylcellulose, gelatin, guar gum, hydrogenated vegetable oil, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, copolyvidone, methyl cellulose, liquid glucose, maltodextrin, polymethacrylates, povidone, pregelatinized starch, sodium alginate, starch, sucrose, tragacanth, and zein.
The compounds may be formulated for parenteral administration by injection, e.g., by bolus injection or continuous infusion. Formulations for injection may be presented in unit dosage form, e.g., in ampoules or in multi-dose containers, with an added preservative. The compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents. The formulations may be presented in unit-dose or multi-dose containers, for example sealed ampoules and vials, and may be stored in powder form or in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example, saline or sterile pyrogen-free water, immediately prior to use. Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described.
Formulations for parenteral administration include aqueous and non-aqueous (oily) sterile injection solutions of the active compounds which may contain antioxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the blood of the intended recipient; and aqueous and non-aqueous sterile suspensions which may include suspending agents and thickening agents. Suitable lipophilic solvents or vehicles include fatty oils such as sesame oil, or synthetic fatty acid esters, such as ethyl oleate or triglycerides, or liposomes. Aqueous injection suspensions may contain substances which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol, or dextran. Optionally, the suspension may also contain suitable stabilizers or agents which increase the solubility of the compounds to allow for the preparation of highly concentrated solutions.
In addition to the formulations described previously, the compounds may also be formulated as a depot preparation. Such long acting formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection. Thus, for example, the compounds may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.
For buccal or sublingual administration, the compositions may take the form of tablets, lozenges, pastilles, or gels formulated in conventional manner. Such compositions may comprise the active ingredient in a flavored basis such as sucrose and acacia or tragacanth.
The compounds may also be formulated in rectal compositions such as suppositories or retention enemas, e.g., containing conventional suppository bases such as cocoa butter, polyethylene glycol, or other glycerides.
Certain compounds disclosed herein may be administered topically, that is by non-systemic administration. This includes the application of a compound disclosed herein externally to the epidermis or the buccal cavity and the instillation of such a compound into the ear, eye and nose, such that the compound does not significantly enter the blood stream. In contrast, systemic administration refers to oral, intravenous, intraperitoneal and intramuscular administration.
Formulations suitable for topical administration include liquid or semi-liquid preparations suitable for penetration through the skin to the site of inflammation such as gels, liniments, lotions, creams, ointments or pastes, and drops suitable for administration to the eye, ear or nose. The active ingredient for topical administration may comprise, for example, from 0.001% to 10% w/w (by weight) of the formulation. In certain embodiments, the active ingredient may comprise as much as 10% w/w. In other embodiments, it may comprise less than 5% w/w. In certain embodiments, the active ingredient may comprise from 2% w/w to 5% w/w. In other embodiments, it may comprise from 0.1% to 2% w/w of the formulation.
Topical ophthalmic, otic, and nasal formulations of the present invention may comprise excipients in addition to the active ingredient. Excipients commonly used in such formulations include, but are not limited to, tonicity agents, preservatives, chelating agents, buffering agents, and surfactants. Other excipients comprise solubilizing agents, stabilizing agents, comfort-enhancing agents, polymers, emollients, pH-adjusting agents and/or lubricants. Any of a variety of excipients may be used in formulations of the present invention including water, mixtures of water and water-miscible solvents, such as C1-C7-alkanols, vegetable oils or mineral oils comprising from 0.5 to 5% non-toxic water-soluble polymers, natural products, such as alginates, pectins, tragacanth, karaya gum, guar gum, xanthan gum, carrageenin, agar and acacia, starch derivatives, such as starch acetate and hydroxypropyl starch, and also other synthetic products such as polyvinyl alcohol, polyvinylpyrrolidone, polyvinyl methyl ether, polyethylene oxide, preferably cross-linked polyacrylic acid and mixtures of those products. The concentration of the excipient is, typically, from 1 to 100,000 times the concentration of the active ingredient. In preferred embodiments, the excipients to be included in the formulations are typically selected on the basis of their inertness towards the active ingredient component of the formulations.
Relative to ophthalmic, otic, and nasal formulations, suitable tonicity-adjusting agents include, but are not limited to, mannitol, dextrose, sodium chloride, glycerin, sorbitol and the like. Suitable buffering agents include, but are not limited to, phosphates, citrates, borates, acetates and the like. Suitable surfactants include, but are not limited to, ionic and nonionic surfactants (though nonionic surfactants are preferred), polysorbate 80, RLM 100, POE 20 cetylstearyl ethers such as Procol® CS20 and poloxamers such as Pluronic® F68. Formulations may contain substances which increase the viscosity of the solution or suspension, such as sodium carboxymethyl cellulose, hypromellose, micro crystalline cellulose, sorbitol, or dextran. Optionally, the formulation may also contain suitable stabilizers or agents which increase the solubility of the compounds to allow for the preparation of highly concentrated solutions, including but not limited to ethanol, benzyl alcohol, polyethylene glycol, phenylethyl alcohol and glycerin.
The formulations set forth herein may comprise one or more preservatives. Examples of such preservatives include benzalkonium chloride, p-hydroxybenzoic acid ester, sodium perborate, sodium chlorite, alcohols such as chlorobutanol, benzyl alcohol or phenyl ethanol, guanidine derivatives such as polyhexamethylene biguanide, sodium perborate, polyquaternium-1, amino alcohols such as AMP-95, or sorbic acid. In certain embodiments, the formulation may be self-preserved so that no preservation agent is required.
For ophthalmic, otic, or nasal administration, the formulation may be a solution, a suspension or a gel. In preferred aspects, the formulations for topical application to the eye or ear are in aqueous solution or suspension in the form of drops. In preferred aspects, the formulations for topical application to the nose in aqueous solution or suspension are in the form of drops, spray or aerosol. The term “aqueous” typically denotes an aqueous formulation wherein the formulation is >50%, more preferably >75% and in particular >90% by weight water. These drops may be delivered from a single dose ampoule which may preferably be sterile and thus render bacteriostatic components of the formulation unnecessary. Alternatively, the drops may be delivered from a multi-dose bottle which may preferably comprise a device which extracts any preservative from the formulation as it is delivered, such devices being known in the art. Solution and suspension formulations may be nasally administered using a nebulizer. Intranasal delivery as a solution, suspension or dry powder may also facilitated by propellant-based aerosol systems, which include but are not limited to hydrofluoroalkane-based propellants.
For ophthalmic disorders, components of the invention may be delivered to the eye as a concentrated gel or a similar vehicle, or as dissolvable inserts that are placed beneath the eyelids.
The formulations of the present invention that are adapted for topical administration to the eye are preferably isotonic, or slightly hypotonic in order to combat any hypertonicity of tears caused by evaporation and/or disease. This may require a tonicity agent to bring the osmolality of the formulation to a level at or near 210-320 milliosmoles per kilogram (mOsm/kg). The formulations of the present invention generally have an osmolality in the range of 220-320 mOsm/kg, and preferably have an osmolality in the range of 235-300 mOsm/kg. The ophthalmic formulations will generally be formulated as sterile aqueous solutions.
In certain ophthalmic embodiments, the compositions of the present invention are formulated with one or more tear substitutes. A variety of tear substitutes are known in the art and include, but are not limited to: monomeric polyols, such as, glycerol, propylene glycol, and ethylene glycol; polymeric polyols such as polyethylene glycol; cellulose esters such hydroxypropylmethyl cellulose, carboxy methylcellulose sodium and hydroxy propylcellulose; dextrans such as dextran 70; vinyl polymers, such as polyvinyl alcohol; and carbomers, such as carbomer 934P, carbomer 941, carbomer 940 and carbomer 974P. Certain formulations of the present invention may be used with contact lenses or other ophthalmic products.
Preferred formulations are prepared using a buffering system that maintains the formulation at a pH of about 4.0 to a pH of about 8. A most preferred formulation pH is from 6.5 to 7.5.
In particular embodiments, a formulation of the present invention is administered once a day. However, the formulations may also be formulated for administration at any frequency of administration, including once a week, once every 5 days, once every 3 days, once every 2 days, twice a day, three times a day, four times a day, five times a day, six times a day, eight times a day, every hour, or any greater frequency. Such dosing frequency is also maintained for a varying duration of time depending on the therapeutic regimen. The duration of a particular therapeutic regimen may vary from one-time dosing to a regimen that extends for months or years. The formulations are administered at varying dosages, but typical dosages are one to two drops at each administration, or a comparable amount of a gel or other formulation. One of ordinary skill in the art would be familiar with determining a therapeutic regimen for a specific indication.
Gels for topical or transdermal administration may comprise, generally, a mixture of volatile solvents, nonvolatile solvents, and water. In certain embodiments, the volatile solvent component of the buffered solvent system may include lower (C1-C6) alkyl alcohols, lower alkyl glycols and lower glycol polymers. In further embodiments, the volatile solvent is ethanol. The volatile solvent component is thought to act as a penetration enhancer, while also producing a cooling effect on the skin as it evaporates. The nonvolatile solvent portion of the buffered solvent system is selected from lower alkylene glycols and lower glycol polymers. In certain embodiments, propylene glycol is used. The nonvolatile solvent slows the evaporation of the volatile solvent and reduces the vapor pressure of the buffered solvent system. The amount of this nonvolatile solvent component, as with the volatile solvent, is determined by the pharmaceutical compound or drug being used. When too little of the nonvolatile solvent is in the system, the pharmaceutical compound may crystallize due to evaporation of volatile solvent, while an excess may result in a lack of bioavailability due to poor release of drug from solvent mixture. The buffer component of the buffered solvent system may be selected from any buffer commonly used in the art; in certain embodiments, water is used. A common ratio of ingredients is about 20% of the nonvolatile solvent, about 40% of the volatile solvent, and about 40% water. There are several optional ingredients which can be added to the topical composition. These include, but are not limited to, chelators and gelling agents. Appropriate gelling agents can include, but are not limited to, semisynthetic cellulose derivatives (such as hydroxypropylmethylcellulose) and synthetic polymers, galactomannan polymers (such as guar and derivatives thereof) and cosmetic agents.
Lotions include those suitable for application to the skin or eye. An eye lotion may comprise a sterile aqueous solution optionally containing a bactericide and may be prepared by methods similar to those for the preparation of drops. Lotions or liniments for application to the skin may also include an agent to hasten drying and to cool the skin, such as an alcohol or acetone, and/or a moisturizer such as glycerol or an oil such as castor oil or arachis oil.
Creams, ointments or pastes are semi-solid formulations of the active ingredient for external application. They may be made by mixing the active ingredient in finely-divided or powdered form, alone or in solution or suspension in an aqueous or non-aqueous fluid, with the aid of suitable machinery, with a greasy or non-greasy base. The base may comprise hydrocarbons such as hard, soft or liquid paraffin, glycerol, beeswax, a metallic soap; a mucilage; an oil of natural origin such as almond, corn, arachis, castor or olive oil; wool fat or its derivatives or a fatty acid such as stearic or oleic acid together with an alcohol such as propylene glycol or a macrogel. The formulation may incorporate any suitable surface active agent such as an anionic, cationic or non-ionic surfactant such as a sorbitan ester or a polyoxyethylene derivative thereof. Suspending agents such as natural gums, cellulose derivatives or inorganic materials such as silicaceous silicas, and other ingredients such as lanolin, may also be included.
Drops or sprays may comprise sterile aqueous or oily solutions or suspensions and may be prepared by dissolving the active ingredient in a suitable aqueous solution of a bactericidal and/or fungicidal agent and/or any other suitable preservative, and, in certain embodiments, including a surface active agent. The resulting solution may then be clarified by filtration, transferred to a suitable container which is then sealed and sterilized by autoclaving or maintaining at 98-100° C. for half an hour. Alternatively, the solution may be sterilized by filtration and transferred to the container by an aseptic technique. Examples of bactericidal and fungicidal agents suitable for inclusion in the drops are phenylmercuric nitrate or acetate (0.002%), benzalkonium chloride (0.01%) and chlorhexidine acetate (0.01%). Suitable solvents for the preparation of an oily solution include glycerol, diluted alcohol and propylene glycol.
Formulations for topical administration in the mouth, for example buccally or sublingually, include lozenges comprising the active ingredient in a flavored basis such as sucrose and acacia or tragacanth, and pastilles comprising the active ingredient in a basis such as gelatin and glycerin or sucrose and acacia.
For administration by inhalation, compounds may be conveniently delivered from an insufflator, nebulizer pressurized packs or other convenient means of delivering an aerosol spray. Pressurized packs may comprise a suitable propellant such as hydrofluoroalkane, dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas. In the case of a pressurized aerosol, the dosage unit may be determined by providing a valve to deliver a metered amount. Alternatively, for administration by inhalation or insufflation, the compounds according to the invention may take the form of a dry powder composition, for example a powder mix of the compound and a suitable powder base such as lactose or starch. The powder composition may be presented in unit dosage form, in for example, capsules, cartridges, gelatin or blister packs from which the powder may be administered with the aid of an inhalator or insufflator.
Preferred unit dosage formulations are those containing an effective dose, as herein below recited, or an appropriate fraction thereof, of the active ingredient.
It should be understood that in addition to the ingredients particularly mentioned above, the formulations described above may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral or intranasal administration may include flavoring agents.
Compounds may be administered orally or via injection at a dose of from 0.1 to 500 mg/kg per day. The dose range for adult humans is generally from 5 mg to 2 g/day. Tablets or other forms of presentation provided in discrete units may conveniently contain an amount of one or more compounds which is effective at such dosage or as a multiple of the same, for instance, units containing 5 mg to 500 mg, usually around 10 mg to 200 mg.
The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
The compounds can be administered in various modes, e.g. orally, topically, or by injection. The precise amount of compound administered to a patient will be the responsibility of the attendant physician. The specific dose level for any particular patient will depend upon a variety of factors including the activity of the specific compound employed, the age, body weight, general health, sex, diets, time of administration, route of administration, rate of excretion, drug combination, the precise disorder being treated, and the severity of the indication or condition being treated. Also, the route of administration may vary depending on the condition and its severity.
In certain instances, it may be appropriate to administer at least one of the compounds described herein (or a pharmaceutically acceptable salt, ester, or prodrug thereof) in combination with another therapeutic agent. By way of example only, if one of the side effects experienced by a patient upon receiving one of the compounds herein is hypertension, then it may be appropriate to administer an anti-hypertensive agent in combination with the initial therapeutic agent. Or, by way of example only, the therapeutic effectiveness of one of the compounds described herein may be enhanced by administration of an adjuvant (i.e., by itself the adjuvant may only have minimal therapeutic benefit, but in combination with another therapeutic agent, the overall therapeutic benefit to the patient is enhanced). Or, by way of example only, the benefit of experienced by a patient may be increased by administering one of the compounds described herein with another therapeutic agent (which also includes a therapeutic regimen) that also has therapeutic benefit. By way of example only, in a treatment for diabetes involving administration of one of the compounds described herein, increased therapeutic benefit may result by also providing the patient with another therapeutic agent for diabetes. In any case, regardless of the disease, disorder or condition being treated, the overall benefit experienced by the patient may simply be additive of the two therapeutic agents or the patient may experience a synergistic benefit.
Non-limiting examples of possible combination therapies include use of certain compounds of the invention with H1R antagonists, H3R antagonists and/or intranasal corticosteroids. Specific, non-limiting examples of possible combination therapies include use of certain compounds of the invention with H1R antagonists such as acrivastine, alcaftadine, antazoline, azelastine, bromazine, brompheniramine, cetirizine, chlorpheniramine, clemastine, desloratidine, diphenhydramine, diphenylpyraline, ebastine, emedastine, epinastine, fexofenadine, hydroxyzine, ketotifen, levocabastine, levocetirizine, loratidine, methdilazine, mizolastine, promethazine, olopatadine, and triprolidine, or intranasal corticosteroids such as fluticasone, budesonide, beclomethasone, mometasone and ciclesonide.
In any case, the multiple therapeutic agents (at least one of which is a compound disclosed herein) may be administered in any order or even simultaneously. If simultaneously, the multiple therapeutic agents may be provided in a single, unified form, or in multiple forms (by way of example only, either as a single pill or as two separate pills). One of the therapeutic agents may be given in multiple doses, or both may be given as multiple doses. If not simultaneous, the timing between the multiple doses may be any duration of time ranging from a few minutes to four weeks.
Thus, in another aspect, certain embodiments provide methods for treating H1R and/or H4R-mediated disorders in a human or animal subject in need of such treatment comprising administering to said subject an amount of a compound disclosed herein effective to reduce or prevent said disorder in the subject, in combination with at least one additional agent for the treatment of said disorder that is known in the art. In a related aspect, certain embodiments provide therapeutic compositions comprising at least one compound disclosed herein in combination with one or more additional agents for the treatment of H1R and/or H4R-mediated disorders.
Specific diseases to be treated by the compounds, compositions, and methods disclosed herein include inflammation and related diseases, including autoimmune diseases. The compounds are useful to treat arthritis, including but not limited to rheumatoid arthritis, spondyloarthropathies, gouty arthritis, osteoarthritis, systemic lupus erythematosus, juvenile arthritis, acute rheumatic arthritis, enteropathic arthritis, neuropathic arthritis, psoriatic arthritis, and pyogenic arthritis. The compounds are also useful in treating osteoporosis and other related bone disorders. These compounds can also be used to treat gastrointestinal conditions such as reflux esophagitis, diarrhea, inflammatory bowel disease, Crohn's disease, gastritis, irritable bowel syndrome and ulcerative colitis. The compounds may also be used in the treatment of upper respiratory inflammation, such as, but not limited to, seasonal allergic rhinitis, non-seasonal allergic rhinitis, acute non-allergic rhinitis, chronic non-allergic rhinitis, Sampter's triad, non-allergic rhinitis with eosinophilia syndrome, nasal polyposis, atrophic rhinitis, hypertrophic rhinitis, membranous rhinitis, vasomotor rhinitis, rhinosinusitis, chronic rhinopharyngitis, rhinorrhea, occupational rhinitis, hormonal rhinitis, drug-induced rhinitis, gustatory rhinitis, as well as pulmonary inflammation, such as that associated with viral infections and cystic fibrosis. In addition, compounds disclosed herein are also useful in organ transplant patients either alone or in combination with conventional immunomodulators.
Moreover, compounds disclosed herein may be used in the treatment of tendonitis, bursitis, skin-related conditions such as psoriasis, allergic dermatitis, atopic dermatitis and other variants of eczema, allergic contact dermatitis, irritant contact dermatitis, seborrhoeic eczema, nummular eczematous dermatitis, autosensitization dermatitis, Lichen Simplex Chronicus, dyshidrotic dermatitis, neurodermatitis, stasis dermatitis, generalized ordinary urticaria, acute allergic urticaria, chronic allergic urticaria, autoimmune urticaria, chronic idiopathic urticaria, drug-induced urticaria, cholinergic urticaria, chronic cold urticaria, dermatographic urticaria, solar urticaria, urticaria pigmentosa, mastocytosis, acute or chronic pruritis associated with skin-localized or systemic diseases and disorders, such as pancreatitis, hepatitis, burns, sunburn, and vitiligo.
Further, the compounds disclosed herein can be used to treat respiratory diseases, including therapeutic methods of use in medicine for preventing and treating a respiratory disease or condition including: asthmatic conditions including allergen-induced asthma, exercise-induced asthma, pollution-induced asthma, cold-induced asthma, and viral-induced-asthma; chronic obstructive pulmonary diseases including chronic bronchitis with normal airflow, chronic bronchitis with airway obstruction (chronic obstructive bronchitis), emphysema, asthmatic bronchitis, and bullous disease; and other pulmonary diseases involving inflammation including bronchioectasis cystic fibrosis, pigeon fancier's disease, farmer's lung, acute respiratory distress syndrome, pneumonia, aspiration or inhalation injury, fat embolism in the lung, acidosis inflammation of the lung, acute pulmonary edema, acute mountain sickness, acute pulmonary hypertension, persistent pulmonary hypertension of the newborn, perinatal aspiration syndrome, hyaline membrane disease, acute pulmonary thromboembolism, heparin-protamine reactions, sepsis, status asthamticus and hypoxia.
The compounds disclosed herein are also useful in treating tissue damage in such diseases as vascular diseases, periarteritis nodosa, thyroiditis, sclerodoma, rheumatic fever, type I diabetes, neuromuscular junction disease including myasthenia gravis, white matter disease including multiple sclerosis, sarcoidosis, nephritis, nephrotic syndrome, Behcet's syndrome, polymyositis, gingivitis, periodontis, hypersensitivity, and swelling occurring after injury.
The compounds disclosed herein can be used in the treatment of otic diseases and otic allergic disorders, including eustachian tube itching.
The compounds disclosed herein can be used in the treatment of ophthalmic diseases, such as ophthalmic allergic disorders, including allergic conjunctivitis, vernal conjunctivitis, vernal keratoconjunctivitis, and giant papillary conjunctivitis, dry eye, glaucoma, glaucomatous retinopathy, diabetic retinopathy, retinal ganglion degeneration, ocular ischemia, retinitis, retinopathies, uveitis, ocular photophobia, and of inflammation and pain associated with acute injury to the eye tissue. The compounds can also be used to treat post-operative inflammation or pain as from ophthalmic surgery such as cataract surgery and refractive surgery. In preferred embodiments, the compounds of the present invention are used to treat an allergic eye disease chosen from allergic conjunctivitis; vernal conjunctivitis; vernal keratoconjunctivitis; and giant papillary conjunctivitis.
Compounds disclosed herein are useful in treating patients with inflammatory pain such as reflex sympathetic dystrophy/causalgia (nerve injury), peripheral neuropathy (including diabetic neuropathy), and entrapment neuropathy (carpel tunnel syndrome). The compounds are also useful in the treatment of pain associated with acute herpes zoster (shingles), postherpetic neuralgia (PHN), and associated pain syndromes such as ocular pain. Pain indications include, but are not limited to, pain resulting from dermal injuriesand pain-related disorders such as tactile allodynia and hyperalgesia. The pain may be somatogenic (either nociceptive or neuropathic), acute and/or chronic.
The present compounds may also be used in co-therapies, partially or completely, in place of other conventional anti-inflammatory therapies, such as together with steroids, NSAIDs, COX-2 selective inhibitors, 5-lipoxygenase inhibitors, LTB4 antagonists and LTA4 hydrolase inhibitors. The compounds disclosed herein may also be used to prevent tissue damage when therapeutically combined with antibacterial or antiviral agents.
Besides being useful for human treatment, certain compounds and formulations disclosed herein may also be useful for veterinary treatment of companion animals, exotic animals and farm animals, including mammals, rodents, and the like. More preferred animals include horses, dogs, and cats.
All references, patents or applications, U.S. or foreign, cited in the application are hereby incorporated by reference as if written herein in their entireties. Where any inconsistencies arise, material literally disclosed herein controls.
The following schemes can be used to practice the present invention.
The invention is further illustrated by the following examples, which may be made my methods known in the art and/or as shown below. Additionally, these compounds may be commercially available.
A 100 mL round bottom flask was charged with 4-chlorobenzene-1,2-diamine (5.3 g, 37 mmol) and diethyl oxalate (31 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the precipitate was collected by filtration, washed with EtOH (20 mL) and dried, to afford 7.0 g (96%) of the product as light yellow solid. 1H NMR (300 MHz, DMSO-d6) δ: 11.96 (br, 2H), 7.11 (m, 3H). MS m/z: 195 (M−H+).
A 50 mL round bottom flask was charged with 6-chloroquinoxaline-2,3(1H,4H)-dione (7.0 g, 36 mmol) and phosphorus oxychloride (16 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was cooled to room temperature and cautiously poured over ice water. The solid was collected by filtration and re-dissolved in EtOAc (150 mL) then washed with brine (100 mL), dried over anhydrous Na2SO4, and concentrated in vacuo, to afford 7.4 g (89%) of the product as light yellow solid. 1H NMR (300 MHz, DMSO-d6) δ: 8.23 (d, J=2.4 Hz, 1H), 8.12 (d, J=8.7 Hz, 1H), 7.97 (dd, J=8.7, 2.4 Hz, 1H).
A 250 mL round bottom flask was charged with 2,3,6-trichloroquinoxaline (4.6 g, 20 mmol) and EtOH (150 mL). To the above was added dropwise hydrazine hydrate (2.2 g, 44 mmol). The resulting solution was stirred overnight at room temperature. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the resulting light yellow solid was collected by filtration, washed with water (50 mL) then ethyl acetate (50 mL), and dried, to give 1.5 g (34%) of the product as pink solid. 1H NMR (300 MHz, DMSO-d6) δ: 9.14 (br, 1H), 7.75 (d, J=8.7 Hz, 1H), 7.66 (s, 1H), 7.39 (d, J=8.7 Hz, 1H). MS m/z: 229 (M+H+).
A 50 mL round bottom flask was charged with 2,6-dichloro-3-hydrazinylquinoxaline (1.5 g, 6.6 mmol) and triethyl orthoformate (18 mL). The resulting mixture was stirred at 100° C. for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the resulting solid was collected by filtration, washed with MeOH (20 mL×2), and dried, to give 1.5 g (96%) of the product as light yellow powder. 1H NMR (300 MHz, DMSO-d6) δ: 10.20 (s, 1H), 8.70 (d, J=2.1 Hz, 1H), 8.06 (d, J=9.0 Hz, 1H), 7.78 (dd, J=9.0, 2.1 Hz, 1H). MS m/z: 239 (M+H+).
A 250 mL 3-necked round bottom flask was charged with 4,8-dichloro-[1,2,4]triazolo[4,3-a]quinoxaline (Example 1, 1.5 g, 6.27 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (2.1 g, 6.90 mmol), K2CO3 (2.6 g, 6.52 mmol), (1,1′-bis(diphenylphosphino)ferrocene)dichloropalladium(II) (0.51 g, 0.63 mmol), 1,4-dioxane (45 mL) and water (15 mL). The resulting mixture was stirred at 80° C. for 2 h under N2 atmosphere. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1). Work-up: the reaction mixture was diluted with EtOAc (150 mL) and washed with brine (100 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 10-40% EtOAc in petroleum ether, to afford 1.8 g (74%) of the product as light yellow crystals. 1H NMR (300 MHz, DMSO-d6) δ: 10.11 (s, 1H), 8.62 (d, J=2.1 Hz, 1H), 8.28 (br, 1H), 7.98 (d, J=9.0 Hz, 1H), 7.69 (dd, J=9.0, 2.1 Hz, 1H), 4.23 (d, J=9.6 Hz, 2H), 3.64-3.59 (m, 2H), 2.77 (br, 2H), 1.45 (s, 9H). MS m/z: 386 (M+H+).
A 50 mL round bottom flask was charged with tert-butyl 4-(8-chloro-[1,2,4]triazolo[4,3-a]quinoxalin-4-yl)-5,6-dihydropyridine-1(2H)-carboxylate (1.05 g, 2.72 mmol) and CH2Cl2 (25 mL). To the above was added dropwise trifluoroacetic acid (2 mL) at 0° C. The resulting solution was stirred at room temperature for 4 h. Reaction progress was monitored by TLC (MeOH/CH2Cl2=1:10). Work-up: the reaction solution was concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel with a 1:10 MeOH/CH2Cl2, to afford 0.67 g (82%) of the product as light yellow crystals. 1H NMR (300 MHz, DMSO-d6) δ: 10.11 (s, 1H), 8.63 (d, J=2.1 Hz, 1H), 8.34 (t, J=3.3 Hz, 1H), 8.00 (d, J=8.7 Hz, 1H), 7.70 (dd, J=8.7, 2.4 Hz, 1H), 3.64 (m, 2H), 3.01 (m, 2H), 2.66 (m, 2H). MS m/z: 286 (M+H+).
A 10 mL round bottom flask was charged with 8-chloro-4-(1,2,3,6-tetrahydropyridin-4-yl)-[1,2,4]triazolo[4,3-a]quinoxaline (140 mg, 0.489 mmol), HCHO (38%, 78 mg, 0.979 mmol), AcOH (35 mg, 0.587 mmol), CH2Cl2 (2 mL) and MeOH (2 mL). To the above was added NaB(OAc)3H (160 mg, 0.734 mmol) in several batches. The resulting mixture was stirred at room temperature for 1.5 h. Reaction progress was monitored by TLC (MeOH/CH2Cl2=1:10). Work-up: the reaction solution was concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel with a 1:10 MeOH/CH2Cl2, to afford 75 mg (55%) of the product as light yellow solid. 1H NMR (300 MHz, CDCl3) δ: 9.24 (s, 1H), 8.46 (t, J=3.6 Hz, 1H), 8.02 (d, J=8.7 Hz, 1H), 7.92 (d, J=2.1 Hz, 1H), 7.60 (dd, J=8.7, 2.1 Hz, 1H), 3.63 (br, 2H), 3.04 (br, 4H), 2.66 (s, 3H). MS m/z: 300 (M+H+).
A 50 mL round bottom flask was charged with tert-butyl 4-(8-chloro-[1,2,4]triazolo[4,3-a]quinoxalin-4-yl)-5,6-dihydropyridine-1(2H)-carboxylate (prepared as in Example 1, 80 mg, 0.21 mmol) and CH2Cl2 (4 mL). To the above was added dropwise trifluoroacetic acid (0.48 g, 4.14 mmol) at 0° C., followed by addition of triethylsilane (150 mg, 1.24 mmol). The resulting solution was stirred room temperature for 3 days. Reaction progress was monitored by TLC (MeOH/CH2Cl2=1:10). Work-up: the reaction solution was concentrated under reduced pressure. The residue was recrystallized from a 1:3 ethyl acetate/hexane, to afford 45 mg (53%) of the product as light yellow solid. 1H NMR (300 MHz, CD3OD) δ: 9.91 (d, J=0.9 Hz, 1H), 8.46 (t, J=2.1 Hz, 1H), 8.07 (d, J=8.7 Hz, 1H), 7.71 (m, 1H), 3.91 (m, 1H), 3.60 (m, 2H), 3.35-3.29 (m, 2H), 2.47-2.29 (m, 4H). MS m/z: 288 (M+H+).
The title compound was prepared as described in Example 2, except that 8-chloro-4-(piperidin-4-yl)-[1,2,4]triazolo[4,3-a]quinoxaline was substituted for 8-chloro-4-(1,2,3,6-tetrahydropyridin-4-yl)-[1,2,4]triazolo[4,3-a]quinoxaline in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.90 (s, 1H), 8.46 (d, J=2.1 Hz, 1H), 8.07 (d, J=8.4 Hz, 1H), 7.72 (dd, J=8.4, 2.1 Hz, 1H), 3.90 (m, 1H), 3.68 (m, 2H), 3.35 (m, 2H), 2.96 (s, 3H), 2.52-2.44 (m, 4H). MS m/z: 302 (M+H+).
A 250 mL 3-necked round bottom flask was charged with 2,3,6-trichloroquinoxaline (described in step 2 of Example 1, 4.46 g, 19.1 mmol) and EtOH (50 mL). To the above was added dropwise a solution of 2-aminoethanol (2.44 g, 40.1 mmol) in EtOH (20 mL) with the temperature maintained below 35° C. The resulting mixture was stirred at room temperature for 4 h and then cooled to 0° C. The precipitate was collected by filtration, washed with a 1:1 n-hexane/EtOAc and dried, to afford 4.0 g (81%) of the product.
A 100 mL round bottom flask was charged with 2-(3,7-dichloroquinoxalin-2-ylamino)ethanol (4.0 g, 15.5 mmol), SOCl2 (20 mL) and CHCl3 (20 mL). The resulting solution was heated at reflux for 2 h then concentrated in vacuo. The residue was co-evaporated several times with CHCl3 then EtOAc. The crude product thus obtained was washed with EtOAc to afford 2.4 g (65%) of the product.
A 50 mL round bottom flask was charged with 4,8-dichloro-1,2-dihydroimidazo[1,2-a]quinoxaline (500 mg, 2.1 mmol), N-methylpiperazine (700 mg, 7.0 mmol) and EtOH (3 mL). The resulting solution was heated at reflux for 16 h then concentrated in vacuo. The residue was purified by flash column chromatography on silica gel to afford 500 mg (79%) of the product. 1H NMR (300 MHz, CDCl3) δ: 7.24 (d, J=8.4 Hz, 1H), 6.93 (dd, J=8.4, 2.4 Hz, 1H), 6.64 (d, J=2.4 Hz, 1H), 4.21-4.09 (m, 6H), 3.92 (m, 2H), 2.54 (m, 4H), 2.34 (s, 3H). MS m/z: 304 (M+H+).
The title compound was prepared as described in Example 5, except that piperazine was substituted for N-methylpiperazine in step 3 of that route. 1H NMR (300 MHz, CD3OD/D2O) δ: 7.82 (d, J=8.7 Hz, 1H), 7.62 (d, J=2.1 Hz, 1H), 7.56 (dd, J=8.7, 2.1 Hz, 1H), 4.81 (m, 2H), 4.32 (m, 2H), 3.79 (m, 4H), 3.47 (m, 4H). MS m/z: 290 (M+H+).
A 250 mL round bottom flask was charged with 8-chloro-4-(4-methylpiperazin-1-yl)-1,2-dihydroimidazo[1,2-a]quinoxaline (Example 5, 300 mg, 0.99 mmol), chloranil (1 g, 4 mmol) and xylene (100 mL). The resulting solution was heated at reflux for 16 h then cooled to room temperature. The reaction mixture was washed several times with diluted aqueous NaOH solution until the aqueous phase became colorless. The organic layer was concentrated under reduced pressure and the residue was purified by flash column chromatography on silica gel to afford 220 mg (74%) of the product. 1H NMR (300 MHz, CDCl3) δ: 7.90 (d, J=1.2 Hz, 1H), 7.66 (d, J=2.1 Hz, 1H), 7.62-7.58 (m, 2H), 7.34 (dd, J=8.7, 2.1 Hz, 1H), 4.42 (m, 4H), 2.61 (m, 4H), 2.37 (s, 3H). MS m/z: 302 (M+H+).
The title compound was prepared as described in Example 7, except that 8-chloro-4-(piperazin-1-yl)-1,2-dihydroimidazo[1,2-a]quinoxaline (Example 7) was substituted for 8-chloro-4-(4-methylpiperazin-1-yl)-1,2-dihydroimidazo[1,2-a]quinoxaline (Example 5) in step 1 of that route. 1H NMR (300 MHz, D2O) δ: 8.01 (d, J=1.2 Hz, 1H), 7.58 (m, 2H), 7.32 (d, J=9.0 Hz, 1H), 7.22 (d, J=1.8 Hz, 1H), 4.24 (m, 4H), 3.41 (m, 4H). MS m/z: 288 (M+H+).
A 500 mL 3-necked round bottom flask was charged with 2,3,6-trichloroquinoxaline (described in step 2 of Example 1, 5.0 g, 21.4 mmol) and EtOH (100 mL). To the above was added dropwise a solution of 2-aminopropan-1-ol (3.7 mL, 47.5 mmol) in EtOH (50 mL). The resulting solution was heated at reflux for 4 h then concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel with 20% EtOAc in petroleum ether, to afford 2.5 g (54%) of the product as a mixture of two isomers.
A 50 mL round bottom flask was charged with the mixture of 2-(3,7-dichloroquinoxalin-2-ylamino)propan-1-ol and 2-(3,6-dichloroquinoxalin-2-ylamino)propan-1-ol (1.8 g, 6.6 mmol), SOCl2 (10 mL) and CHCl3 (10 mL). The resulting solution was heated at reflux for 2 h then concentrated in vacuo. The residue was poured into saturated aqueous Na2CO3 and extracted with CH2Cl2. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 2% EtOAc in petroleum ether to afford 1.08 g (64%) of 4,8-dichloro-2-methyl-1,2-dihydroimidazo[1,2-a]quinoxaline (1H NMR (300 MHz, CDCl3) δ: 8.15 (d, J=8.7 Hz, 1H), 7.00 (dd, J=8.4, 2.1 Hz, 1H), 6.68 (d, J=2.4 Hz, 1H), 4.50 (m, 1H), 4.16 (m, 1H), 3.60 (m, 1H), 1.44 (d, J=6.6 Hz, 3H)), and 270 mg (0.16%) of 4,7-dichloro-2-methyl-1,2-dihydroimidazo[1,2-a]quinoxaline (1H NMR (300 MHz, CDCl3) δ: 7.57 (d, J=1.8 Hz, 1H), 7.33 (dd, J=8.4, 2.1 Hz, 1H), 6.65 (d, J=8.4 Hz, 1H), 4.52 (m, 1H), 4.20 (m, 1H), 3.62 (m, 1H), 1.45 (d, J=6.9 Hz, 3H)) as yellow solids.
A 50 mL round bottom flask was charged with 4,8-dichloro-2-methyl-1,2-dihydroimidazo[1,2-a]quinoxaline (300 mg, 1.2 mmol), N-methylpiperazine (0.16 mL, 1.4 mmol), Et3N (0.35 mL, 2.5 mmol) and anhydrous EtOH (20 mL). The resulting solution was heated at reflux for 2 h then concentrated in vacuo. The residue was dissolved in CH2Cl2, washed with brine, dried over MgSO4, and concentrated in vacuo, to afford 360 mg (96%) of the product as yellow oil. 1H NMR (300 MHz, DMSO-d6) δ: 7.15 (d, J=8.7 Hz, 1H), 6.92 (dd, J=8.4, 2.4 Hz, 1H), 6.85 (d, J=2.1 Hz, 1H), 4.77 (m, 1H), 4.35 (m, 1H), 3.99 (m, 4H), 3.49 (m, 1H), 2.37 (m, 4H), 2.19 (s, 3H), 1.28 (d, J=6.0 Hz, 1H). MS m/z: 317 (M+H+).
A 50 mL round bottom flask was charged with 8-chloro-2-methyl-4-(4-methylpiperazin-1-yl)-1,2-dihydroimidazo[1,2-a]quinoxaline (360 mg, 1.13 mmol), 2,3-dichloro-5,6-dicyano-p-benzoquinone (515 mg, 2.26 mmol) and xylene (10 mL). The resulting solution was heated at reflux for 3 h then concentrated in vacuo. The residue was dissolved in 1 M aqueous NaOH (10 mL) and extracted with CH2Cl2. The organic layer was dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 3% MeOH in CH2Cl2, to afford 95 mg (26%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 7.60 (m, 3H), 7.31 (dd, J=8.7, 2.4 Hz, 1H), 4.40 (br, 4H), 2.62 (m, 4H), 2.46 (d, J=0.6 Hz, 3H), 2.38 (s, 3H). MS m/z: 315 (M+H+).
The title compound was prepared as described in Example 9, except that piperazine was substituted for N-methylpiperazine in step 3 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.17 (s, 1H), 8.05 (d, J=2.1 Hz, 1H), 7.65 (d, J=8.7 Hz, 1H), 7.41 (dd, J=8.7, 2.4 Hz, 1H), 4.51 (t, J=5.4 Hz, 4H), 3.40 (t, J=5.4 Hz, 4H), 2.45 (s, 3H). MS m/z: 301 (M+H+).
The title compound was prepared as described in Example 9, except that 4,7-dichloro-2-methyl-1,2-dihydroimidazo[1,2-a]quinoxaline was substituted for 4,8-dichloro-2-methyl-1,2-dihydroimidazo[1,2-a]quinoxaline in step 3 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.06 (s, 1H), 7.85 (d, J=8.4 Hz, 1H), 7.59 (d, J=2.4 Hz, 1H), 7.26 (dd, J=9.0, 2.4 Hz, 1H), 4.33 (m, 4H), 2.62 (t, J=5.4 Hz, 4H), 2.43 (s, 3H), 2.35 (s, 3H). MS m/z: 315 (M+H+).
A 250 mL round bottom flask was charged with 2-amino-5-chlorobenzoic acid (17.2 g, 0.1 mol) and urea (30 g, 0.5 mol). The resulting mixture was heated to 200° C. for 3 h. Work up: the reaction mixture was washed by water and filtered. The solid was dried to give 18.5 g (94%) of the product. MS m/z: 196 (M+H+).
The title compound was prepared as described in Example 1, except that 6-chloroquinazoline-2,4(1H,3H)-dione was substituted for 6-chloroquinoxaline-2,3(1H,4H)-dione in step 2 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.24 (d, J=2.1 Hz, 1H), 7.99-7.90 (m, 2H).
A 100 mL round bottom flask was charged with 2,4,6-trichloroquinazoline (1 g, 4.3 mmol) and ethanol (50 mL). To the above was added dropwise hydrazine hydrate (0.492 g, 9.8 mmol) at 0-5° C. The resulting mixture was stirred for 0.5 h below 10° C. then 2 h at room temperature. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:4, Rf=0.3). Work-up: the resulting solid was collected by filtration, washed with ethanol and dried, to give 0.94 g (96%) of the product. 1H NMR (300 MHz, DMSO-d6) δ: 8.34 (s, 1H), 7.76 (m, 1H), 7.58 (m, 1H). MS m/z: 229 (M+H+).
A 250 mL round bottom flask was charged with 2,6-dichloro-4-hydrazinylquinazoline (1 g, 4.4 mmol), piperazine (1.13 g, 13.1 mmol) and absolute ethanol (100 mL). The resulting mixture was heated at reflux for 8 h. Work-up: the reaction mixture was concentrated under reduced pressure. The resulting solid was collected by filtration, washed with ethanol and dried, to give 0.9 g (74%) of the product. MS m/z: 279 (M+H+).
A 250 mL round bottom flask was charged with 6-chloro-4-hydrazinyl-2-(piperazin-1-yl)quinazoline (1.6 g, 5.75 mmol) and 0.2 M HCl (80 mL). To the above was added dropwise a solution of NaNO2 (0.6 g, 8.62 mmol) in water (2 mL) at 0-5° C. The resulting mixture was stirred at 5° C. for 1 h. Work up: the reaction mixture was washed with ethyl acetate (50 mL×3). The aqueous layer was basified to PH 8 by saturated aqueous Na2CO3. The precipitate was collected by filtration, washed with water and dried, to give 670 mg (40%) of the product. 1H NMR (300 MHz, DMSO-d6) δ: 8.36 (d, J=2.4 Hz, 1H), 7.84 (dd, J=9.0, 2.4 Hz, 1H), 7.72 (d, J=9.0 Hz, 1H), 3.98 (m, 4H), 2.92 (m, 4H). MS m/z: 290 (M+H+).
The title compound was prepared as described in Example 12, except that N-methylpiperazine was substituted for piperazine in step 4 of that route. MS m/z: 304 (M+H+).
The title compound was prepared as described in Collection of Czechoslovak Chemical Communications (1984), 49(8), 1795-9, using 6-chloro-4-hydrazinyl-2-(4-methylpiperazin-1-yl)quinazoline described in step 3 of Example 12. MS m/z: 303 (M+H+).
The title compound was obtained from a commercial source.
A 100 mL round bottom flask was charged with 2,3,6-trichloroquinoxaline (described in step 2 of Example 1, 1.0 g, 4.27 mmol), NaN3 (2.5 g, 38.46 mmol) and EtOH (50 mL). The resulting mixture was stirred at 60° C. overnight. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was concentrated under reduced pressure. The residue was mixed with water (30 mL) and extracted with EtOAc (50 and 20 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous Na2SO4, concentrated in vacuo, to afford 1.0 g (quantitative) of the product as yellow amorphous powder. 1H NMR (300 MHz, CDCl3) δ: 8.76 (d, J=2.1 Hz, 1H), 8.70 (d, J=9.0 Hz, 1H), 7.96 (dd, J=9.0, 2.1 Hz, 1H).
A 5 mL microwave reaction tube was charged with 4,7-dichlorotetrazolo[1,5-a]quinoxaline (0.27 g, 1.13 mmol), piperazine (0.15 g, 1.69 mmol), Cs2CO3 (1.14 g, 3.39 mmol) and DMF (4 mL). The resulting mixture was heated at 140° C. for 1 h in a Biotage microwave reactor. Work-up: the reaction mixture was diluted with EtOAc (30 mL) and washed with H2O (30 mL). The organic layer was dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 5-10% MeOH in CH2Cl2 to provide 0.25 g of yellow solid. It was further purified by recrystallization from EtOAc, to afford 120 mg (37%) of the product as light yellow solid. 1H NMR (300 MHz, CD3OD) δ: 8.29 (d, J=8.7 Hz, 1H), 7.71 (d, J=2.4 Hz, 1H), 7.43 (dd, J=8.7, 2.4 Hz, 1H), 4.37 (br, 4H), 3.02 (m, 4H). MS m/z: 290 (M+H+).
The title compound was prepared as described in Example 16, except that N-methylpiperazine was substituted for piperazine in step 2 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.29 (d, J=8.7 Hz, 1H), 7.76 (d, J=2.1 Hz, 1H), 7.38 (dd, J=8.7, 2.1 Hz, 1H), 4.50 (br, 4H), 2.61 (t, J=5.1 Hz, 4H), 2.34 (s, 3H). MS m/z: 304 (M+H+).
A 250 mL round bottom flask was charged with 4-methylbenzene-1,2-diamine (9.76 g, 0.08 mol) and diethyl oxalate (86 mL, 0.64 mol). The resulting mixture was heated at 140° C. overnight. Work-up: the reaction mixture was filtered and the solid was washed with ethanol and dried to give 13 g (92%) of the product. MS m/z: 175 (M+H+).
The title compound was prepared as described in Example 1, except that 6-methylquinoxaline-2,3(1H,4H)-dione was substituted for 6-chloroquinoxaline-2,3(1H,4H)-dione in step 2 of that route. 1H NMR (300 MHz, CDCl3) δ: 7.92 (m, 1H), 7.79 (s, 1H), 7.54 (m, 1H), 2.59 (s, 3H).
The title compound was prepared as described in Example 12, except that 2,3-dichloro-6-methylquinoxaline was substituted for 2,4,6-trichloroquinazoline in step 3 of that route. MS m/z: 209 (M+H+).
The title compound was prepared as described in Example 12, except that 2-chloro-3-hydrazinyl-6-methylquinoxaline was substituted for 2,6-dichloro-4-hydrazinylquinazoline in step 4 of that route. MS m/z: 259 (M+H+).
The title compound was prepared as described in Example 12, except that 3-hydrazinyl-6-methyl-2-(piperazin-1-yl)quinoxaline was substituted for 6-chloro-4-hydrazinyl-2-(piperazin-1-yl)quinazoline in step 5 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.04 (s, 1H), 7.55 (d, J=8.7 Hz, 1H), 7.38 (m, 1H), 4.28 (m, 4H), 3.03 (m, 4H), 2.50 (s, 3H). MS m/z: 270 (M+H+).
The title compound was prepared as described in Example 12, except that 2,6-dichloro-3-hydrazinylquinoxaline (prepared in Example 1) was substituted for 2,6-dichloro-4-hydrazinylquinazoline in step 4 of that route. MS m/z: 279 (M+H+).
The title compound was prepared as described in Example 12, except that 6-chloro-3-hydrazinyl-2-(piperazin-1-yl)quinoxaline was substituted for 6-chloro-4-hydrazinyl-2-(piperazin-1-yl)quinazoline in step 5 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.42 (d, J=2.4 Hz, 1H), 7.80 (d, J=9.0 Hz, 1H), 7.68 (dd, J=9.0, 2.4 Hz, 1H), 4.64 (m, 4H), 3.46 (m, 4H). MS m/z: 290 (M+H+).
The title compound was prepared as described in Example 19, except that N-methylpiperazine was substituted for piperazine in step 1 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.37 (d, J=2.7 Hz, 1H), 7.68 (d, J=8.7 Hz, 1H), 7.55 (dd, J=8.7, 2.4 Hz, 1H), 4.43 (br, 4H), 2.62 (m, 4H), 2.38 (s, 3H). MS m/z: 304 (M+H+).
A 100 mL round bottom flask was charged with 2-chloro-3-hydrazinyl-6-methylquinoxaline (prepared in Example 18 step 1-3, 2.39 g, 11.4 mmol) and trimethyl orthoformate (40 mL). The resulting mixture was heated at reflux for 1.5 h. Work-up: the reaction mixture was filtered and the solid was washed with ethanol and dried to give 1.55 g (62%) of the product. MS m/z: 219 (M+H+).
The title compound was prepared as described in Example 12, except that 4-chloro-8-methyl-[1,2,4]triazolo[4,3-a]quinoxaline was substituted for 2,6-dichloro-4-hydrazinylquinazoline, and N-methylpiperazine for piperazine in step 4 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.15 (s, 1H), 7.56 (m, 2H), 7.28 (m, 1H), 4.42 (br, 4H), 2.59 (m, 4H), 2.48 (s, 3H), 2.35 (s, 3H). MS m/z: 283 (M+H+).
The title compound was prepared as described in Example 21, except that piperazine was substituted for N-methylpiperazine in step 2 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.14 (s, 1H), 7.55 (m, 2H), 7.29 (m, 1H), 4.41 (br, 4H), 3.10 (m, 4H), 2.50 (s, 3H). MS m/z: 269 (M+H+).
A 100 mL round bottom flask was charged with 4-(trifluoromethyl)benzene-1,2-diamine (5.3 g, 37 mmol) and diethyl oxalate (31 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the precipitate was collected by filtration, washed with EtOH (20 mL) and dried, to afford 7.0 g (96%) of the product as light yellow solid.
A 100 mL round bottom flask was charged with 6-(trifluoromethyl)-1,4-dihydroquinoxaline-2,3-dione (7.0 g, 36 mmol) and phosphorus oxychloride (16 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was cooled to room temperature and cautiously poured into ice water. The solid was collected by filtration and re-dissolved in EtOAc (150 mL) then washed with brine (100 mL), dried over anhydrous Na2SO4, and concentrated in vacuo, to afford 7.4 g (89%) of the product as light yellow solid.
A 250 mL round bottom flask was charged with 2,3-dichloro-6-(trifluoromethyl)quinoxaline (4.6 g, 17.2 mmol) and EtOH (50 mL). To the above was added dropwise N-methylpiperazine (1.7 g, 17.2 mmol). The resulting solution was stirred overnight at room temperature. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in EtOAc (50 mL) and washed with brine (20 mL). The organic layer was dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 10-20% EtOAc in petroleum ether, to afford 3.0 g (52%) of the product as white solid. MS m/z: 331 (M+H+).
A 100 mL round bottom flask was charged with 3-chloro-2-(4-methylpiperazinyl)-6-(trifluoromethyl)quinoxaline (3.0 g, 9.1 mmol), hydrazine hydrate (9.0 g, 182 mmol) and EtOH (50 mL). The resulting solution was refluxed for 0.5 h. Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in CH2Cl2 (50 mL) and washed with brine (20 mL). The organic layer was dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with a 1:10 MeOH/CH2Cl2, to afford 1.5 g (50%) of the product as light yellow crystals. MS m/z: 327 (M+H+).
A 100 mL round bottom flask was charged with 3-hydrazinyl-2-(4-methylpiperazin-1-yl)-6-(trifluoromethyl)quinoxaline (1.3 g, 3.9 mmol) and triethyl orthoformate (20 mL). The resulting mixture was stirred at 100° C. for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=2:1). Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in EtOAc (50 mL) and washed with brine (20 mL). The organic layer was dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 10-40% EtOAc in petroleum ether, to afford 0.7 g (54%) of the product as white solid. 1H NMR (300 MHz, CD3OD) δ: 9.91 (s, 1H), 8.45 (s, 1H), 7.73 (m, 2H), 4.49 (m, 4H), 2.69 (m, 4H), 2.39 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Example 23, except that piperazine was substituted for N-methylpiperazine in step 3 of that route. 1H NMR (300 MHz, CD3OD) δ: 10.10 (s, 1H), 8.57 (s, 1H), 7.82 (m, 2H), 4.73 (m, 4H), 3.46 (m, 4H). MS m/z: 323 (M+H+).
The title compound was prepared as described in Examples 50 and 21, except that 4-(trifluoromethyl)benzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 9.81 (s, 1H), 8.20 (d, J=8.7 Hz, 1H), 7.53 (d, J=2.1 Hz, 1H), 7.56 (dd, J=8.7, 2.1 Hz, 1H), 4.46 (m, 4H), 2.67 (m, 4H), 2.37 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Example 25, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 9.87 (s, 1H), 8.25 (d, J=8.1 Hz, 1H), 7.94 (d, J=1.5 Hz, 1H), 7.64 (dd, J=8.7, 1.8 Hz, 1H), 4.60 (m, 4H), 2.67 (m, 4H). MS m/z: 323 (M+H+).
The title compound was prepared as described in Examples 23 and 16, except that 3-chloro-2-(4-methylpiperazinyl)-6-(trifluoromethyl)quinoxaline (prepared as described in Example 90 step 3) was substituted for 2,3,6-trichloroquinoxaline in step 1 of Example 16. 1H NMR (300 MHz, CD3OD) δ: 8.62 (s, 1H), 7.88 (m, 2H), 4.49-4.46 (m, 4H), 2.68 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 338 (M+H+).
The title compound was prepared as described in Example 27, except that 2-chloro-3-(4-methylpiperazinyl)-6-(trifluoromethyl)quinoxaline was obtained in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.35 (d, J=8.7 Hz, 1H), 7.86 (d, J=0.9 Hz, 1H), 7.63 (dd, J=8.7, 0.9 Hz, 1H), 4.42-4.38 (br, 4H), 2.67 (t, J=5.1 Hz, 4H), 2.39 (s, 3H). MS m/z: 338 (M+H+).
The title compound was prepared as described in Example 27, except that tert-butyl piperazinecarboxylate was substituted for N-methylpiperazine and tert-butyl 4-[3-chloro-6-(trifluoromethyl)quinoxalin-2-yl]piperazinecarboxylate was obtained in step 1 of that route. BOC group was then removed by methanolic HCl in EtOAc. 1H NMR (300 MHz, CD3OD) δ: 8.70 (d, J=2.1 Hz, 1H), 7.97 (d, J=9.0 Hz, 1H), 7.93 (dd, J=9.0, 2.1 Hz, 1H), 4.74-4.70 (br, 4H), 3.48 (t, J=5.1 Hz, 4H). MS m/z: 324 (M+H+).
The title compound was prepared as described in Example 29, except that tert-butyl 4-[3-chloro-7-(trifluoromethyl)quinoxalin-2-yl]piperazinecarboxylate was obtained in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.61 (d, J=8.4 Hz, 1H), 8.13 (d, J=1.8 Hz, 1H), 7.83 (dd, J=8.4, 1.8 Hz, 1H), 4.70 (t, J=5.1 Hz, 4H), 3.48 (t, J=5.1 Hz, 4H). MS m/z: 324 (M+H+).
The title compound was prepared as described in Example 23, except that 4-chloro-5-fluorobenzene-1,2-diamine was substituted for 4-(trifluoromethyl)benzene-1,2-diamine in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.80 (s, 1H), 8.36 (d, J=7.2 Hz, 1H), 7.53 (d, J=9.9 Hz, 1H), 5.45-3.28 (m, 8H), 2.97 (s, 3H). MS m/z: 321 (M+H+).
The title compound was prepared as described in Example 31, except that piperazine was substituted for N-methylpiperazine in step 3 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.86 (s, 1H), 8.39 (d, J=7.2 Hz, 1H), 7.54 (d, J=9.9 Hz, 1H), 4.67 (t, J=5.1 Hz, 4H), 3.42 (t, J=5.1 Hz, 4H). MS m/z: 307 (M+H+).
The title compound was prepared as described in Examples 50 and 21, except that 5-chloro-4-fluorobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, DMSO-d6) δ: 9.93 (s, 1H), 8.38 (d, J=9.9 Hz, 1H), 7.72 (d, J=7.2 Hz, 1H), 4.30-4.27 (m, 4H), 3.34-3.31 (m, 4H), 2.23 (s, 3H). MS m/z: 321 (M+H+).
A 100 mL round bottom flask was charged with 4-fluoro-3-methylaniline (9.0 g, 0.072 mol) and acetyl acetate (32 mL). The resulting mixture was stirred 1 h at 0° C. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the reaction solution was diluted with H2O (100 mL) and neutralized with ammonia. The precipitate was collected by filtration, washed with H2O, and dried under vacuum, to afford 12 g (quantitative yield) of product as white solids. MS m/z: 168 (M+H+).
A 100 mL round bottom flask was charged with N-(4-fluoro-3-methylphenyl)acetamide (10.5 g, 0.063 mol) and nitric acid (68%, 15 mL). To the solution was added dropwise fuming nitric acid (12 mL). The reaction solution was stirred 1 h at room temperature. Work-up: the reaction solution was diluted with H2O (100 mL). The precipitate was collected by filtration, washed with H2O, and dried under vacuum. It was further purified by column chromatography on silica gel with a 1:20 EtOAc/CH2Cl2, giving 8.47 g (64%) of the product as yellow solids. 1H NMR (300 MHz, CDCl3) δ: 10.28 (s, 1H), 8.65 (d, J=6.6 Hz, 1H), 7.87 (d, J=9.3 Hz, 1H), 2.36 (d, J=2.1 Hz, 3H), 2.28 (s, 3H).
A 250 mL round bottom flask was charged with N-(4-fluoro-5-methyl-2-nitrophenyl)acetamide (4.0 g, 0.019 mol), KOH (1.06 g, 0.019 mol), H2O (30 mL) and MeOH (80 mL). The solution was kept in a 60° C. water-bath for 15 min. H2O (30 mL) was added and the reaction mixture was kept in the bath for another 15 min before it was cooled in an ice-bath. The precipitates were collected by filtration, washed with cold water, and dried under vacuum, giving 3.15 g (98%) of the product as orange solids.
A 250 mL round bottom flask was charged with 4-fluoro-5-methyl-2-nitrophenylamine (3.12 g, 0.018 mol), Na2S2O4 (9.58 g, 0.055 mol), H2O (45 mL) and EtOH (90 mL). The mixture was heated at reflux for 1 h. Work-up: the solvent was evaporated. The residue was suspended in triethylamine (15 mL) and ethyl acetate (300 mL), and then filtered. The filtrate was concentrated in vacuo, giving 2.1 g (82%) of the product as pale-red solids.
The title compound was prepared as described in Example 23, except that 5-fluoro-4-methylbenzene-1,2-diamine was substituted for 4-(trifluoromethyl)benzene-1,2-diamine in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.68 (s, 1H), 7.93 (d, J=7.5 Hz, 1H), 7.25 (d, J=10.8 Hz, 1H), 4.38 (m, 4H), 2.64 (t, J=4.9 Hz, 4H), 2.39 (s, 3H), 2.37 (s, 3H). MS m/z: 301 (M+H+).
The title compound was prepared as described in Example 34, except that piperazine was substituted for N-methylpiperazine in step 7 of that route. 1H NMR (300 MHz, D2O) δ: 8.40 (s, 1H), 7.36 (d, J=8.1 Hz, 1H), 7.00 (d, J=10.5 Hz, 1H), 3.92 (t, J=5.1 Hz, 4H), 3.35 (t, J=5.1 Hz, 4H), 2.19 (s, 3H). MS m/z: 287 (M+H+).
The title compound was prepared as described in Examples 50 and 21, except that 5-fluoro-4-methylbenzene-1,2-diamine (prepared in Example 34 step 1-4) was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CDCl3) δ: 9.05 (s, 1H), 7.62 (d, J=7.8 Hz, 1H), 7.37 (d, J=8.7 Hz, 1H), 4.42 (m, 4H), 2.60 (t, J=4.8 Hz, 4H), 2.37 (s, 6H). MS m/z: 301 (M+H+).
The title compound was prepared as described in Examples 50 and 21, except that 4,5-difluorobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 9.67 (s, 1H), 8.08 (dd, J=10.5, 7.5 Hz, 1H), 7.45 (dd, J=11.4, 7.8, 1H), 4.38 (m, 4H), 2.63 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 305 (M+H+).
The title compound was prepared as described in Example 37, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 9.68 (s, 1H), 8.09 (dd, J=10.5, 7.8 Hz, 1H), 7.46 (dd, J=11.7, 7.8 Hz, 1H), 4.35 (t, J=4.8 Hz, 4H), 2.99 (t, J=5.1 Hz, 4H). MS m/z: 291 (M+H+).
The title compound was prepared as described in Example 23, except that 4,5-dichlorobenzene-1,2-diamine was substituted for 4-(trifluoromethyl)benzene-1,2-diamine in step 1 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.09 (s, 1H), 7.80 (s, 1H), 7.76 (s, 1H), 4.50-4.47 (m, 4H), 2.59 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Example 34, except that 4-fluoro-3-trifluoromethylaniline was substituted for 4-fluoro-3-methylaniline in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.95 (s, 1H), 8.54 (d, J=6.0 Hz, 1H), 7.56 (d, J=12.0 Hz, 1H), 4.88-4.82 (m, 4H), 3.52-3.47 (m, 4H), 2.97 (s, 3H). MS m/z: 355 (M+H+).
The title compound was prepared as described in Example 40, except that N-BOC piperazine was substituted for N-methylpiperazine. 1H NMR (300 MHz, CD3OD) δ: 9.86 (s, 1H), 8.44 (d, J=6.0 Hz, 1H), 7.41 (d, J=12.0 Hz, 1H), 4.47-4.43 (m, 4H), 3.02-2.99 (m, 4H). MS m/z: 341 (M+H+).
The title compound was prepared as described in Examples 50 and 21, except that 5-fluoro-4-trifluoromethylbenzene-1,2-diamine (prepared in Example 40 step 1-4) was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 9.77 (s, 1H), 8.14 (d, J=12.0 Hz, 1H), 7.90 (d, J=9.0 Hz, 1H), 4.43-4.40 (m, 4H), 2.67-2.64 (m, 4H), 2.38 (s, 3H). MS m/z: 355 (M+H+).
The title compound was prepared as described in Example 42, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 9.75 (s, 1H), 8.11 (d, J=12.0 Hz, 1H), 7.86 (d, J=9.0 Hz, 1H), 4.39-4.36 (m, 4H), 3.00-2.96 (m, 4H). MS m/z: 341 (M+H+).
The title compound was prepared as described in Example 34 step 1-4, except that 4-chloro-3-trifluoromethylaniline was substituted for 4-fluoro-3-methylaniline as the starting material of that route.
The title compound was prepared as described in Examples 50 and 21, except that 4-chloro-5-(trifluoromethyl)benzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 9.81 (s, 1H), 8.39 (s, 1H), 7.95 (s, 1H), 4.46 (m, 4H), 2.64 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 371 (M+H+).
The title compound was prepared as described in Example 44, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 10.12 (s, 1H), 8.73 (s, 1H), 7.96 (s, 1H), 4.58 (m, 4H), 3.28 (m, 4H). MS m/z: 357 (M+H+).
The title compound was prepared as described in Example 23, except that 4-chloro-5-(trifluoromethyl)benzene-1,2-diamine (prepared in Example 44 step 1-4) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 9.89 (s, 1H), 8.49 (s, 1H), 7.71 (s, 1H), 4.50 (m, 4H), 2.64 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 371 (M+H+).
The title compound was prepared as described in Example 46, except that piperazine was substituted for N-methylpiperazine in step 3 of that route. 1H NMR (300 MHz, CD3OD) δ: 10.22 (s, 1H), 8.76 (s, 1H), 7.80 (s, 1H), 4.64 (m, 4H), 3.21 (m, 4H). MS m/z: 357 (M+H+).
The title compound was prepared as described in Example 34, except that 2-fluoro-4-trifluoromethylaniline was substituted for 4-fluoro-3-methylaniline in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.89 (s, 1H), 8.29 (s, 1H), 7.53 (d, J=9.3 Hz, 1H), 4.52 (m, 4H), 2.66 (d, J=4.8 Hz, 4H), 2.37 (s, 3H). MS m/z: 355 (M+H+).
The title compound was prepared as described in Example 48, except that piperazine was substituted for N-methylpiperazine in step 7 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.86 (s, 1H), 8.24 (s, 1H), 7.48 (d, J=9.9 Hz, 1H), 4.45 (m, 4H), 3.00 (m, 4H). MS m/z: 341 (M+H+).
The title compound was prepared as described in Examples 50 and 21, except that 4-(trifluoromethoxy)benzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, DMSO-d6) δ: 10.03 (s, 1H), 8.34 (d, J=1.2 Hz, 1H), 7.65 (d, J=9.0 Hz, 1H), 7.45 (dd, J=9.0, 1.2 Hz, 1H), 4.31 (br, 4H), 2.49-2.46 (m, 4H), 2.22 (s, 3H). MS m/z: 353 (M+H+).
The HCl salt of the title compound was prepared as described in Example 50, except that piperazine was substituted for N-methylpiperazine in step 5 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 10.01 (s, 1H), 8.32 (s, 1H), 7.63 (d, J=8.4 Hz, 1H), 7.43 (d, J=8.7 Hz, 1H), 4.25 (br, 4H), 2.84 (br, 4H). MS m/z: 339 (M+H+).
The title compound was prepared as described in Examples 50 and 21, except that 4-bromobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material, and N-BOC piperazine for N-methylpiperazine in the last step of that route. It was separated from the other regio-isomer by column chromatography on silica gel with a 1:1:2 EtOAc/CH2Cl2/petroleum ether. 1H NMR (300 MHz, CDCl3) δ: 9.14 (s, 1H), 7.88 (m, 1H), 7.56 (m, 2H), 4.42 (m, 4H), 3.63 (m, 4H), 1.50 (s, 9H).
The title compound was prepared as described in Examples 50 and 21, except that 4-bromobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material, and N-BOC piperazine for N-methylpiperazine in the last step of that route. It was separated from the other regio-isomer by column chromatography on silica gel with a 1:1:2 EtOAc/CH2Cl2/petroleum ether. 1H NMR (300 MHz, CDCl3) δ: 9.14 (s, 1H), 7.85 (d, J=2.1 Hz, 1H), 7.59 (d, J=8.7 Hz, 1H), 7.41 (dd, J=8.7, 2.1 Hz, 1H), 4.44 (m, 4H), 3.63 (t, J=5.1 Hz, 4H), 1.50 (s, 9H).
A 50 mL round bottom flask was charged with tert-butyl 4-(8-bromo-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate (0.13 g, 0.28 mmol), THF (15 mL) and concentrate HCl (0.5 mL). The reaction mixture was heated at reflux for 1 h. Work-up: the solid was collected by filtration, washed with THF, and dried under vacuum, giving 0.11 g (99%) of the product as white solids. 1H NMR (300 MHz, D2O) δ: 9.19 (s, 1H), 7.49 (d, J=1.8 Hz, 1H), 7.15 (dd, J=6.6, 2.1 Hz, 1H), 6.98 (d, J=5.7 Hz, 1H), 4.27 (t, J=5.1 Hz, 4H), 3.37 (t, J=5.1 Hz, 4H). MS m/z: 333 (M+H+).
The HCl salt of the title compound was prepared as described in Example 52, except that tert-butyl 4-(7-bromo-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate was substituted for tert-butyl 4-(8-bromo-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate in the last step of that route. 1H NMR (300 MHz, D2O) δ: 9.30 (s, 1H), 7.26 (d, J=8.7 Hz, 1H), 7.22 (s, 1H), 7.04 (d, J=8.4 Hz, 1H), 4.29 (t, J=5.4 Hz, 4H), 3.36 (t, J=5.1 Hz, 4H). MS m/z: 333 (M+H+).
A 100 mL round bottom flask was charged with 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (1.30 g, 3.6 mmol), formaldehyde (40%, 6 mL), CH2Cl2 (20 mL), MeOH (20 mL) and NaBH3(CN) (0.68 g, 0.011 mol). The resulting mixture was stirred at room temperature for 1 h. Work-up: the reaction mixture was diluted with H2O (100 mL) and extracted with CH2Cl2 (50 mL×2). The combined organic layers was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by column chromatography on silica gel with 3% MeOH in CH2Cl2, giving 0.94 g (77%) of the product as white solids. 1H NMR (300 MHz, CDCl3) δ: 9.12 (s, 1H), 7.89 (m, 1H), 7.63 (m, 2H), 4.46 (m, 4H), 2.60 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 347 (M+H+).
The title compound was obtained from commercial sources.
The title compound was prepared analogously to Example 54. MS m/z: 389 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 289 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 269 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 289 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 303 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 329 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 329 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 275 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 329 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 329 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 303 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 301 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 317 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 315 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 263 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 333 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 276 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 303 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 304 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 290 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 318 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 291 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 305 (M+H+).
The title compound was prepared analogously to Example 54. MS m/z: 277 (M+H+).
The title compound was prepared analogously to Example 54. MS M/Z: 278 (M+H+).
The title compound was prepared analogously to Example 54. MS M/Z: 303 (M+H+).
The title compound was prepared analogously to Example 54. MS M/Z: 317 (M+H+).
The title compound was prepared analogously to Example 54. MS M/Z: 317 (M+H+).
The title compound was prepared analogously to Example 54. MS M/Z: 317 (M+H+).
The title compound was prepared analogously to Example 54. MS M/Z: 303 (M+H+).
The title compound was prepared analogously to Example 54. MS M/Z: 331 (M+H+).
The title compound was prepared analogously to Example 54. MS M/Z: 345 (M+H+).
A 100 mL round bottom flask was charged with 8-bromo-4-(4-methylpiperazinyl)-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline (Example 54, 0.86 g, 2.48 mmol), LiCl (0.21 g, 5.0 mmol), tri-n-butyl(vinyl)tin (0.94 g, 3.0 mmol), bis(triphenyphosphine)palladium(II) chloride (0.12 g, 0.2 mmol) and DMF (25 mL). The mixture was heated at 90° C. overnight. Work-up: the reaction solution was diluted with H2O (100 mL) and extracted with EtOAc (100 mL×2). The combined organic layers was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by column chromatography on silica gel with 4% MeOH in CH2Cl2, giving 0.48 g (66%) of the product as white solids. 1H NMR (300 MHz, CDCl3) δ: 9.17 (s, 1H), 7.68-7.61 (m, 3H), 6.78 (dd, J=17.4, 11.1 Hz, 1H), 5.82 (d, J=17.4 Hz, 1H), 5.34 (d, J=11.1 Hz, 1H), 4.46 (m, 4H), 2.60 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 295 (M+H+).
The HCl salt of the title compound was prepared as described in Example 52, except that tert-butyl 4-(8-vinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate (prepared as described in Example 88 from tert-butyl 4-(8-bromo-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate) was substituted for tert-butyl 4-(8-bromo-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate in step 6 of that route. 1H NMR (300 MHz, D2O) δ: 8.89 (s, 1H), 6.68 (m, 3H), 6.08 (dd, J=17.4, 10.8 Hz, 1H), 5.36 (d, J=17.4 Hz, 1H), 5.06 (d, J=10.8 Hz, 1H), 4.07 (t, J=5.1 Hz, 4H), 3.28 (t, J=5.1 Hz, 4H). MS m/z: 281 (M+H+).
A 100 mL round bottom flask was charged with 4-(4-methylpiperazinyl)-8-vinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline (Example 88, 0.26 g, 0.88 mol), Pd/C (0.10 g) and THF (30 mL). The mixture was stirred under H2 atmosphere for 1 h. Work-up: The reaction mixture was filtered. The filtrate was concentrated in vacuo, giving 0.18 g (69%) of the product as white solids. 1H NMR (300 MHz, CDCl3) δ: 9.17 (s, 1H), 7.61 (d, J=8.4 Hz, 1H), 7.62 (d, J=1.8 Hz, 1H), 7.31 (dd, J=8.4, 1.8 Hz, 1H), 4.43 (m, 4H), 2.79 (q, J=7.5 Hz, 2H), 2.60 (t, J=6.0 Hz, 4H), 2.37 (s, 3H), 1.32 (t, J=7.5 Hz, 3H). MS m/z: 297 (M+H+).
The HCl salt of the title compound was prepared as described in Example 52, except that tert-butyl 4-(8-ethyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate (prepared as described in Example 90 and 88 from tert-butyl 4-(8-bromo-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate) was substituted for tert-butyl 4-(8-bromo-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate in step 6 of that route. 1H NMR (300 MHz, D2O) δ: 9.17 (s, 1H), 7.10-6.98 (m, 3H), 4.19 (t, J=4.8 Hz, 1H), 3.37 (t, J=5.4 Hz, 4H), 2.45 (q, J=7.5 Hz, 2H), 1.05 (t, J=7.5 Hz, 3H). MS m/z: 283 (M+H+).
A 100 mL round bottom flask was charged with 2-amino-5-chlorobenzonitrile (0.76 g, 5.0 mmol), methyl chloroformate (0.43 mL, 5.40 mmol), NaHCO3 (0.5 g, 6.0 mmol) and 2-butanone (25 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was filtered and the solid was washed more 2-butanone (20 mL×2). The filtrate was concentrated in vacuo, to give 0.95 g (97%) of the product as white solid.
A 100 mL round bottom flask was charged with methyl 4-chloro-2-cyanophenylcarbamate (0.9 g, 4.26 mmol), formic hydrazide (0.3 g, 5.12 mmol) and 1-methyl-2-pyrrolidone (25 mL). The resulting mixture was heated at 180° C. for 1.5 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the solvent was evaporated under reduced pressure and the residue was poured into EtOAc (20 mL) and well-mixed by stirring. The solid was collected by filtration, washed with EtOAc (20 mL) and dried, to give 0.88 g (85%) of the product as light yellow crystalline solid. 1H NMR (300 MHz, DMSO-d6) δ: 12.45 (s, 1H), 8.55 (s, 1H), 8.12 (d, J=2.4 Hz, 1H), 7.75 (dd, J=9.0, 2.4 Hz, 1H), 7.45 (d, J=9.0 Hz, 1H). MS m/z: 219 (M−H+).
A 50 mL round bottom flask was charged with 9-chloro-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one (0.88 g, 4.0 mmol) and phosphorus oxychloride (15 mL). To the above was added dropwise N,N-diisopropylethylamine (1.38 g, 8.0 mmol). The resulting mixture was heated at reflux for 8 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:8). Work-up: the solvent was evaporated under reduced pressure and the residue was poured into EtOAc (20 mL) and well-mixed by stirring. The solid was collected by filtration, washed with CH2Cl2 (20 mL), and dried, to give 0.77 g (81%) of the product as light yellow crystalline solid. 1H NMR (300 MHz, CDCl3) δ: 8.51 (dd, J=2.4, 0.3 Hz, 1H), 8.48 (s, 1H), 7.97 (d, J=9.0 Hz, 1H), 7.81 (dd, J=9.0, 2.4 Hz, 1H). MS m/z: 239 (M+H+).
A 5 mL microwave reaction tube was charged with 5,9-dichloro-[1,2,4]triazolo[1,5-c]quinazoline (0.12 g, 0.50 mmol), piperazine (0.103 g, 0.55 mmol) and EtOH (4 mL). The resulting mixture was heated at 130° C. for 1.5 h in a Biotage microwave reactor. Work-up: the solvent was evaporated under reduced pressure. The solid was collected by filtration, washed with H2O (10 mL) and dried, to give 0.18 g (92%) of the product as light yellow crystalline solid. 1H NMR (300 MHz, CD3OD) δ: 8.52 (s, 1H), 8.32 (m, 1H), 7.75 (m, 2H), 4.33 (t, J=5.1 Hz, 4H), 3.48 (t, J=5.4 Hz, 4H). MS m/z: 289 (M+H+).
A 10 mL round bottom flask was charged with 2-amino-4-chlorobenzonitrile (0.2 g, 1.31 mmol), N-chlorosuccinimide (0.19 g, 1.44 mmol) and DMF (5 mL). The resulting mixture was stirred at 25° C. overnight. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was diluted with EtOAc (40 mL) and washed with brine (40 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a 1:10 EtOAc/Petroleum ether, to afford 170 mg (47%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 7.45 (s, 1H), 6.88 (s, 1H), 4.48 (br, 2H).
The title compound was prepared as described in Example 92, except that N-methylpiperazine was substituted for piperazine in step 4,2-amino-4,5-dichlorobenzonitrile for 2-amino-5-chlorobenzonitrile in step 1, and acetic hydrazide for formic hydrazide in step 2. 1H NMR (300 MHz, CD3OD) δ: 8.26 (s, 1H), 7.77 (s, 1H), 4.12 (t, J=5.1 Hz, 4H), 2.67 (t, J=5.1 Hz, 4H), 2.58 (s, 3H), 2.38 (s, 3H). MS m/z: 351 (M+H+).
The title compound was prepared as described in Example 93, except that piperazine was substituted for N-methylpiperazine in step 5 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.22 (s, 1H), 7.73 (s, 1H), 4.08 (m, 4H), 3.06 (m, 4H), 2.58 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Example 93, except that 2-amino-4-fluorobenzonitrile was substituted for 2-amino-4-chlorobenzonitrile in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.22 (d, J=8.1 Hz, 1H), 7.42 (d, J=10.5 Hz, 1H), 4.12 (t, J=4.8 Hz, 4H), 2.66 (t, J=4.8 Hz, 4H), 2.57 (s, 3H), 2.37 (s, 3H). MS m/z: 335 (M+H+).
The title compound was prepared as described in Example 95, except that piperazine was substituted for N-methylpiperazine in step 5 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.26 (d, J=7.8 Hz, 1H), 7.46 (d, J=10.8 Hz, 1H), 4.08 (m, 4H), 3.03 (m, 4H), 2.58 (s, 3H). MS m/z: 321 (M+H+).
A 100 mL round bottom flask was charged with 4,5-difluoro-2-nitrobenzoic acid (5.08 g, 25 mmol) and SOCl2 (15 mL). The mixture was refluxed for 1 h then concentrated in vacuo. To the residue was added slowly 25% aqueous ammonia (30 mL) at 0° C. and the reaction mixture was stirred for further 2 h at 0° C. The reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1, Rf=0.4). Work-up: the solid was collected by filtration and dried to afford 4.06 g (80%) of the product as brown solid.
A 250 mL round bottom flask was charged with 4,5-difluoro-2-nitrobenzamide (4.06 g, 20 mmol), (CF3C0)2O (5.6 mL, 40 mmol), Et3N (5.6 mL, 40 mmol) and CH2Cl2 (120 mL). The resulting mixture was stirred for 1 h at room temperature. The reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:4, Rf=0.7). Work-up: the reaction mixture was diluted with more CH2Cl2 (120 mL), washed with saturated aqueous NaHCO3 (250 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. The oil residue solidified after 1 h at room temperature, to afford 4.5 g (quantitative yield) of the product as orange solid. 1H NMR (300 MHz, DMSO-d6) δ: 8.70 (dd, J=10.3, 7.3 Hz, 1H), 8.58 (dd, J=10.1, 7.5 Hz, 1H).
A 250 mL round bottom flask was charged with 4,5-difluoro-2-nitrobenzonitrile (3.68 g, 20 mmol), Na2S2O4 (85% purity, 8.19 g, 40 mmol), EtOH (150 mL) and H2O (20 mL). The resulting mixture was stirred at reflux overnight and then concentrated to dryness under reduced pressure. The residue was suspended in saturated aqueous NaHCO3 (200 mL) and extracted with ethyl ether (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 then concentrated in vacuo, to afford 1.2 g (39%) of the product as yellow solid. 1H NMR (300 MHz, DMSO-d6) δ: 7.64 (dd, J=10.8, 8.9 Hz, 1H), 6.72 (dd, J=13.1, 7.1 Hz, 1H), 6.24 (br, 2H).
A 100 mL round bottom flask was charged with 2-amino-4,5-difluorobenzonitrile (1.1 g, 7.1 mmol), ethyl chloroformate (25 mL, 260 mmol) and NaHCO3 (0.72 g, 8.6 mmol). The resulting mixture was refluxed overnight (16 h) then cooled to room temperature. It was diluted with CH2Cl2 (200 mL) then filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel with 10% AcOEt in petroleum ether, to afford 1.36 g (84%) of the product as white solid. 1H NMR (300 MHz, DMSO-d6) δ: 9.91 (s, 1H), 8.11 (dd, J=10.4, 8.5 Hz, 1H), 7.65 (dd, J=12.1, 7.4 Hz, 1H), 4.16 (q, J=7.1 Hz, 2H), 1.25 (t, J=7.1 Hz, 3H).
A 50 mL round bottom flask was charged with ethyl 2-cyano-4,5-difluorophenylcarbamate (1.36 g, 6.0 mmol), acetic hydrazide (0.535 g, 7.2 mmol) and 1-methyl-2-pyrrolidone (15 mL). The resulting solution was refluxed for 2 h. The 1-methyl-2-pyrrolidone was then removed under reduced pressure, to afford 1.42 g (quantitative) of the product as orange solid. It was used directly in the next step.
A 100 mL round bottom flask was charged with 8,9-difluoro-2-methyl-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one (1.42 g, 6.0 mmol) and POCl3 (20 mL). After N,N-diisopropylethylamine (2.1 mL, 12 mmol) was added dropwise at 0° C., the resulting mixture was refluxed overnight (16 h) and then concentrated under reduced pressure. The residue was carefully diluted with saturated aqueous NaHCO3 (150 mL), then extracted with CH2Cl2 (150 mL×2). The combined organic layers were washed with brine (150 mL), dried over anhydrous Na2SO4 then concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 20-50% AcOEt in CH2Cl2 (containing 1% Et3N), to afford 0.96 g (63%) of the product as light-orange solid. 1H NMR (300 MHz, CDCl3) δ: 8.19 (dd, J=9.4, 8.1 Hz, 1H), 7.75 (dd, J=10.3, 7.1 Hz, 1H), 2.66 (s, 3H).
A 100 mL round bottom flask was charged with 5-chloro-8,9-difluoro-2-methyl-[1,2,4]triazolo[1,5-c]quinazoline (0.2 g, 0.8 mmol), N-methylpiperazine (0.1 mL, 0.9 mmol), Et3N (0.5 mL, 3.6 mmol), DMF (10 mL) and THF (10 mL). The resulting solution was stirred at room temperature for 1 h, and then was concentrated under reduced pressure. The residue was mixed with saturated aqueous NaHCO3 (100 mL), then extracted with CHCl3 (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 2-4% MeOH in CH2Cl2 (saturated with NH3), to afford 0.085 g (34%) of the product as off-white solid. 1H NMR (300 MHz, CDCl3) δ: 8.05 (dd, J=9.8, 8.5 Hz, 1H), 7.46 (dd, J=11.4, 7.2 Hz, 1H), 4.09 (t, J=4.8 Hz, 4H), 2.66 (t, J=4.8 Hz, 4H), 2.62 (s, 3H), 2.40 (s, 3H). MS m/z: 319 (M+H+).
The title compound was prepared as described in Example 97, except that piperazine was substituted for N-methylpiperazine in step 7 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.05 (dd, J=9.9, 8.4 Hz, 1H), 7.46 (dd, J=11.4, 7.1 Hz, 1H), 4.01 (t, J=5.1 Hz, 4H), 3.10 (t, J=5.1 Hz, 4H), 2.62 (s, 3H). MS m/z: 305 (M+H+).
A 100 mL round bottom flask was charged with 2-amino-5-methylbenzonitrile (3.5 g, 26.5 mmol), Na2CO3 (5.8 g, 54.7 mmol) and methyl chloroformate (50 mL). The resulting solution was heated at reflux overnight. The reaction mixture was concentrated. The resulting precipitate was collected by filtration, to afford 2.6 g (52%) of the product as yellow solid.
A 100 mL round bottom flask was charged with methyl 2-cyano-4-methylphenylcarbamate (2.6 g, 13.7 mmol), acetic hydrazide (1.2 g, 16.2 mmol) and 1-methyl-2-pyrrolidone (50 mL). The resulting solution was heated at 180° C. for 1 h then concentrated in vacuo. The resulting precipitate was collected by filtration, washed with EtOAc and dried, to afford 2 g (68%) of the product.
A 100 mL round bottom flask was charged with 2,9-dimethyl-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one (1 g, 1.07 mmol), N,N-dimethylanaline (0.26 mL, 2.14 mmol) and POCl3 (10 mL). The resulting solution was heated at reflux for 3 h then concentrated in vacuo. The residue was poured into saturated aqueous Na2CO3 and extracted with CH2Cl2. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 300 mg (27%) of the product as white solid. MS m/z: 233 (M+H+).
A 20 mL microwave reaction tube was charged with 5-chloro-2,9-dimethyl-[1,2,4]triazolo[1,5-c]quinazoline (150 mg, 0.64 mmol), N-methylpiperazine (0.22 mL, 1.98 mmol) and anhydrous EtOH (10 mL). The resulting solution was heated at 130° C. for 1 h in a Biotage microwave reactor. The solvent was evaporated and the residue was purified by flash column chromatography on silica gel with 10% MeOH in CH2Cl2 to afford 110 mg (57%) of the product as white solid. 1H NMR (300 MHz, CD3OD) δ: 8.00 (s, 1H), 7.53 (m, 2H), 3.99 (br, 4H), 2.66 (t, J=5.1 Hz, 4H), 2.57 (s, 3H), 2.48 (s, 3H), 2.37 (s, 3H). MS m/z: 297 (M+H+).
The title compound was prepared as described in Example 99, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.06 (d, J=1.2 Hz, 1H), 7.63 (d, J=8.7 Hz, 1H), 7.56 (dd, J=8.4, 1.5 Hz, 1H), 3.93 (m, 4H), 3.04 (m, 4H), 2.59 (s, 3H), 2.50 (s, 3H). MS m/z: 283 (M+H+).
A 100 mL round bottom flask was charged with 5-methoxy-2-nitrobenzoic acid (1.5 g, 7.61 mmol), DMF (1 mL) and SOCl2 (15 mL). The resulting mixture was heated at reflux for 1 h then concentrated in vacuo. The residue was re-dissolved in DMF (3 mL) and the solution was added dropwise to aqueous ammonia (25%, 15 mL) at 0° C. with vigorous stirring. Work-up: the resulting solid was collected by filtration, washed with H2O (20 mL) and dried, to give 1.2 g (80%) of the product as white solid.
A 100 mL round bottom flask was charged with 5-methoxy-2-nitrobenzamide (2.1 g, 0.01 mol), trifluoroacetic anhydride (2.2 mL), triethylamine (2.9 mL) and CH2Cl2 (30 mL). The resulting solution was stirred at room temperature for 1 h. Work-up: the reaction solution was washed with H2O (30 mL×2). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo, to give 1.75 g (92%) of the product as white solid. MS m/z: 179 (M+H+).
A 100 mL round bottom flask was charged with 5-methoxy-2-nitrobenzonitrile (1.7 g, 9.55 mmol), sodium dithionite (4.99 g, 29 mmol), water (15 mL) and EtOH (50 mL). The resulting mixture was heated at reflux for 1 h. Work-up: the reaction mixture was concentrated in vacuo to remove ethanol then extracted with EtOAc (50 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 1.4 g (quantitative) of the product as yellow oil. It was used in the next step without further purification.
The title compound was prepared as described in Examples 92, except that N-methylpiperazine was substituted for piperazine in step 4,2-amino-5-methoxybenzonitrile for 2-amino-5-chlorobenzonitrile in step 1, and acetic hydrazide for formic hydrazide in step 2. 1H NMR (300 MHz, CDCl3) δ: 7.67 (m, 2H), 7.29 (dd, J=9.0, 2.7 Hz, 1H), 3.99 (m, 4H), 3.93 (s, 3H), 2.68 (m, 4H), 2.65 (s, 3H), 2.40 (s, 3H). MS m/z: 313 (M+H+).
The title compound was prepared as described in Example 101, except that piperazine was substituted for N-methylpiperazine in step 7 of that route. 1H NMR (300 MHz, CD3OD) δ: 7.66 (m, 2H), 7.32 (dd, J=9.0, 3.0 Hz, 1H), 3.96-3.92 (m, 7H), 3.12 (t, J=5.1 Hz, 4H), 2.59 (s, 3H). MS m/z: 299 (M+H+).
The title compound was prepared as described in Examples 92, except that N-methylpiperazine was substituted for piperazine in step 4,2-amino-5-(trifluoromethyl)benzonitrile for 2-amino-5-chlorobenzonitrile in step 1, and acetic hydrazide for formic hydrazide in step 2. 1H NMR (300 MHz, CD3OD) δ: 8.52 (s, 1H), 7.89 (dd, J=9.0, 2.4 Hz, 1H), 7.78 (dd, J=9.0, 0.6 Hz, 1H), 4.19 (t, J=5.1 Hz, 4H), 2.67 (t, J=5.1 Hz, 4H), 2.60 (s, 3H), 2.37 (s, 3H). MS m/z: 351 (M+H+).
The title compound was prepared as described in Example 103, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.45 (d, J=0.3 Hz, 1H), 7.85 (dd, J=8.7, 2.4 Hz, 1H), 7.72 (d, J=8.7 Hz, 1H), 4.11 (m, 4H), 3.02 (t, J=4.8 Hz, 4H), 2.57 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Examples 92, except that N-methylpiperazine was substituted for piperazine in step 4,2-amino-4-chlorobenzonitrile for 2-amino-5-chlorobenzonitrile in step 1, and acetic hydrazide for formic hydrazide in step 2. 1H NMR (300 MHz, CDCl3) δ: 8.23 (d, J=8.7 Hz, 1H), 7.71 (d, J=2.1 Hz, 1H), 7.37 (dd, J=8.7, 2.1 Hz, 1H), 4.12 (m, 4H), 2.63 (m, 7H), 2.38 (s, 3H). MS m/z: 317 (M+H+).
The title compound was prepared as described in Example 105, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.23 (d, J=8.4 Hz, 1H), 7.72 (d, J=1.8 Hz, 1H), 7.38 (dd, J=8.7, 2.1 Hz, 1H), 4.17 (t, J=4.8 Hz, 4H), 3.20 (t, J=4.8 Hz, 4H), 2.63 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared as described in Example 101, except that 4-fluoro-2-nitrobenzoic acid was substituted for 5-methoxy-2-nitrobenzoic acid in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.26 (dd, J=8.7, 6.0 Hz, 1H), 7.35 (dd, J=10.5, 2.4 Hz, 1H), 7.24 (m, 1H), 4.12 (m, 4H), 2.68 (m, 4H), 2.58 (s, 3H), 2.37 (s, 3H). MS m/z: 301 (M+H+).
The title compound was prepared as described in Example 107, except that piperazine was substituted for N-methylpiperazine in step 7 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.25 (dd, J=9.0, 6.0 Hz, 1H), 7.33 (dd, J=10.5, 2.7 Hz, 1H), 7.22 (m, 1H), 4.05 (m, 4H), 3.30 (m, 4H), 2.58 (s, 3H). MS m/z: 287 (M+H+).
The title compound was prepared as described in Example 101, except that 2-nitro-4-(trifluoromethyl)benzoic acid was substituted for 5-methoxy-2-nitrobenzoic acid in step 1 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.40 (d, J=8.4 Hz, 1H), 7.92 (s, 1H), 7.59 (d, J=8.4 Hz, 1H), 4.14 (br, 4H), 2.65 (m, 7H), 2.38 (s, 3H). MS m/z: 351 (M+H+).
The title compound was prepared as described in Example 109, except that piperazine was substituted for N-methylpiperazine in step 7 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.35 (d, J=8.4 Hz, 1H), 7.92 (s, 1H), 7.63 (dd, J=8.4, 1.5 Hz, 1H), 4.08 (m, 4H), 3.04 (m, 4H), 2.60 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Examples 92, except that N-methylpiperazine was substituted for piperazine in step 4. 1H NMR (300 MHz, CDCl3) δ: 8.29 (d, J=2.4 Hz, 1H), 7.61 (m, 2H), 4.08 (br, 4H), 2.64 (m, 7H), 2.38 (s, 3H). MS m/z: 317 (M+H+).
The title compound was prepared as described in Example 111, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. MS m/z: 317 (M+H+).
The title compound was prepared as described in Example 111, except that 5,9-dichloro-2-methyl-[1,2,4]triazolo[1,5-c]quinazoline was substituted for 5,9-dichloro-[1,2,4]triazolo[1,5-c]quinazoline in the final step of that route. 1H NMR (300 MHz, CD3OD) δ: 8.19 (s, 1H), 7.67 (m, 2H), 4.01 (m, 4H), 3.03 (t, J=5.1 Hz, 4H), 2.59 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared as described in Examples 92, except that N-methylpiperazine was substituted for piperazine in step 4, and propionic hydrazide for formic hydrazide in step 2. 1H NMR (300 MHz, CDCl3) δ: 8.30 (d, J=2.1 Hz, 1H), 7.60 (m, 2H), 4.09 (br, 4H), 2.97 (q, J=7.5 Hz, 2H), 2.65 (t, J=4.8 Hz, 4H), 2.38 (s, 3H), 1.44 (t, J=7.8 Hz, 3H). MS m/z: 331 (M+H+).
The title compound was prepared as described in Example 114, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.15 (s, 1H), 7.59 (s, 2H), 4.01 (t, J=5.1 Hz, 4H), 3.03 (t, J=4.8 Hz, 4H), 2.94 (q, J=7.5 Hz, 2H), 1.42 (t, J=7.2 Hz, 3H). MS m/z: 317 (M+H+).
The title compound was prepared as described in Example 92, except that N-methylpiperazine was substituted for piperazine in step 4, and isobutyric hydrazide for formic hydrazide in step 2. 1H NMR (300 MHz, CD3OD) δ: 8.25 (t, J=1.5 Hz, 1H), 7.63 (d, J=1.5 Hz, 2H), 4.09 (t, J=4.5 Hz, 4H), 3.29 (m, 1H), 2.67 (t, J=4.5 Hz, 4H), 2.37 (s, 3H), 1.45 (d, J=6.9 Hz, 6H). MS m/z: 345 (M+H+).
The title compound was prepared as described in Example 116, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.27 (m, 1H), 7.65 (m, 2H), 4.04 (m, 4H), 3.29 (m, 1H), 3.03 (m, 4H), 1.45 (d, J=6.9 Hz, 6H). MS m/z: 331 (M+H+).
A 100 mL round bottom flask was charged with 2-amino-5-chlorobenzonitrile (0.76 g, 5.0 mmol), methyl chloroformate (0.43 mL, 5.40 mmol), NaHCO3 (0.5 g, 6.0 mmol) and 2-butanone (25 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was filtered and the solid was washed more 2-butanone (20 mL×2). The filtrate was concentrated in vacuo, to give 0.95 g (97%) of the product as white solid.
A 50 mL round bottom flask was charged with methyl 4-chloro-2-cyanophenylcarbamate (500 mg, 2.38 mmol), 2-phenylacetic hydrazide (430 mg, 2.86 mmol) and 1-methyl-2-pyrrolidone (20 mL). The resulting solution was heated at 180° C. for 1.5 h then concentrated in vacuo. The resulting precipitate was collected by filtration, washed with EtOAc and dried, to afford 610 mg (82%) of the product.
A 50 mL round bottom flask was charged with 2-benzyl-9-chloro-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one (610 mg, 1.97 mmol) and POCl3 (15 mL). The resulting solution was heated at reflux for 1 h then concentrated in vacuo. The residue was poured into saturated aqueous Na2CO3 and extracted with CH2Cl2. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 330 mg (51%) of the product as white solid.
A 50 mL round bottom flask was charged with 2-benzyl-5,9-dichloro-[1,2,4]triazolo[1,5-c]quinazoline (160 mg, 0.488 mmol), Et3N (0.14 mL, 1.0 mmol), N-methylpiperazine (0.07 ml, 0.65 mmol) and anhydrous EtOH (15 mL). The resulting solution stirred at room temperature for 1.5 h then concentrated in vacuo. The resulting solid was washed with H2O to give 115 mg (60%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 8.31 (d, J=2.1 Hz, 1H), 7.62 (d, J=8.7 Hz, 1H), 7.56 (dd, J=9.0, 2.4 Hz, 1H), 7.43-7.24 (m, 5H), 4.29 (s, 2H), 4.08 (m, 4H), 2.64 (t, J=4.8 Hz, 4H), 2.38 (s, 3H). MS m/z: 393 (M+H+).
The title compound was prepared as described in Example 118, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.23 (s, 1H), 7.64 (m, 2H), 7.38-7.21 (m, 5H), 4.27 (s, 2H), 4.02 (t, J=4.8 Hz, 4H), 3.02 (t, J=4.8 Hz, 4H). MS m/z: 379 (M+H+).
A 25 mL round bottom flask was charged with 2-amino-5-(trifluoromethyl)benzenecarbonitrile (1.0 g, 5.4 mmol), Na2CO3 (1.14 g, 10.8 mmol) and ethyl chloroformate (15 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:6). Work-up: the mixture was filtered and the filter cake was washed 2-butanone (20 mL×2). The filtrate was concentrated to dryness, giving 1.35 g (98%) of the product as light yellow solids.
A 25 mL round bottom flask was charged with N-[2-cyano-4-(trifluoromethyl)phenyl]ethoxycarboxamide (0.3 g, 1.2 mmol), hydrazine hydrate (0.07 g, 1.4 mmol) and THF (7 mL). The resulting mixture was heated at 60° C. overnight. Work-up: the precipitate was collected by filtration and washed with THF (20 mL×2), to afford 0.15 g (52%) of the product as light yellow solids. The filtrate was recovered and heated again at 60° C., to get another batch of 50 mg of the product in the same manner. MS m/z: 245 (M+H+).
A 15 mL tube was charged with 3-amino-4-imino-6-(trifluoromethyl)-3,4-dihydroquinazolin-2(1H)-one (0.24 g, 1.0 mmol) and trifluoroacetic anhydride (3 mL). The tube was sealed and the reaction mixture was heated at 85° C. overnight. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=2:1). Work-up: the solvent was evaporated under reduced pressure. The crude material was purified by flash column chromatography on silica gel with a 1:40 MeOH/CH2Cl2, to afford 0.29 g (91%) of the product as light yellow crystals. 1H NMR (300 MHz, DMSO-d6) δ: 11.14 (s, 1H), 8.71 (d, J=1.8 Hz, 1H), 8.00 (dd, J=8.7, 1.8 Hz, 1H), 7.76 (d, J=8.7 Hz, 1H). MS m/z: 321 (M−H+).
A 25 mL round bottom flask was charged with 2,9-bis(trifluoromethyl)-5,7-dihydro-1,2,4-triazolo[1,5-c]quinazolin-6-one (0.16 g, 0.50 mmol) and phosphorus oxychloride (4 mL). To the resulting solution was added N,N-diisopropylethylamine (0.17 mL, 1.0 mmol). The mixture was heated at reflux for 1.5 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=2:1). Work-up: the solvent was evaporated under reduced pressure. The crude material was purified by flash column chromatography on silica gel with a 1:15 EtOAc/Petroleum ether, to afford 0.16 g (95%) of the product as light yellow solids.
A 25 mL round bottom flask was charged with N-methylpiperazine (0.11 mL, 0.94 mmol) and acetonitrile (2 mL). To the resulting solution was added dropwise a solution of 5-chloro-2,9-bis(trifluoromethyl)-[1,2,4]triazolo[1,5-c]quinazoline (0.16 g, 0.47 mmol) in acetonitrile (2 mL). The mixture was stirred at room temperature for 30 minutes. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:8). Work-up: the solvent was evaporated under reduced pressure. The residue was mixed with water (10 mL) and stirred for 20 minutes at room temperature. The solid was collected by filtration, washed with water (5 mL), and dried, to give 0.17 g (90%) of the product as light yellow crystals. 1H NMR (300 MHz, CD3OD) δ: 8.63 (d, J=1.8 Hz, 1H), 7.99 (dd, J=9.0, 1.8 Hz, 1H), 7.87 (d, J=9.0 Hz, 1H), 4.19 (t, J=4.5 Hz, 4H), 2.70 (t, J=4.5 Hz, 4H), 2.38 (s, 3H). MS m/z: 405 (M+H+).
The title compound was prepared as described in Example 120, except that piperazine was substituted for N-methylpiperazine in step 5 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.61 (d, J=0.6 Hz, 1H), 7.95 (dd, J=8.7, 0.6 Hz, 1H), 7.85 (d, J=8.7 Hz, 1H), 4.14 (t, J=4.8 Hz, 4H), 3.07 (t, J=4.8 Hz, 4H). MS m/z: 391 (M+H+).
A 250 mL 3-necked round bottom flask was charged with 3-chloro-4-(trifluoromethyl)aniline (4.5 g, 0.02 mol) and MeOH (50 mL). To the above was added dropwise a solution of IC1 (4.8 g, 0.03 mol) in CH2Cl2 (100 mL) at 0° C. The resulting mixture was stirred at room temperature for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:20, Rf=0.6). Work-up: the mixture was concentrated in vacuo. The residue was re-dissolved in CH2Cl2, washed with water, dried over anhydrous Na2SO4 and concentrated in vacuo, to give 6.9 g (93%) of the product. MS m/z: 320 (M−H+).
A 250 mL round bottom flask was charged with 5-chloro-2-iodo-4-(trifluoromethyl)aniline (6.9 g, 0.02 mol), CuCN (3.85 g, 0.04 mol) and DMF (100 mL). The resulting mixture was stirred at 130° C. overnight. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:4, Rf=0.5). Work-up: the mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 20% EtOAc in petroleum ether, to afford 3 g (63%) of the product. MS m/z: 221 (M+H+).
The HCl salt of the title compound was prepared as described in Example 93, except that 2-amino-4-chloro-5-(trifluoromethyl)benzenecarbonitrile was substituted for 2-amino-4,5-dichlorobenzonitrile in steps 2-5 of that route. 1H NMR (300 MHz, D2O) δ: 7.87 (s, 1H), 7.36 (s, 1H), 4.94-4.91 (m, 2H), 3.53-3.51 (m, 4H), 3.25-3.22 (m, 2H), 2.90 (s, 3H), 2.45 (s, 3H). MS m/z: 385 (M+H+).
The HCl salt of the title compound was prepared as described in Example 122, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, D2O) δ: 7.83 (s, 1H), 7.32 (s, 1H), 4.18 (t, J=5.4 Hz, 4H), 3.04 (t, J=4.8 Hz, 4H), 2.45 (s, 3H). MS m/z: 371 (M+H+).
The title compound was prepared as described in Example 122, except that 3-fluoro-4-(trifluoromethyl)aniline was substituted for 3-chloro-4-(trifluoromethyl)aniline in step 1 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 11.65 (s, 1H), 8.43 (d, J=8.1 Hz, 1H), 7.67 (d, J=12.6 Hz, 1H), 5.08 (d, J=12.9 Hz, 2H), 3.75-3.24 (m, 6H), 2.78 (s, 3H), 2.55 (s, 3H). MS m/z: 369 (M+H+).
The title compound was prepared as described in Example 124, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 9.45 (s, 2H), 8.47 (d, J=7.8 Hz, 1H), 7.69 (d, J=12.3 Hz, 1H), 4.35 (t, J=4.5 Hz, 4H), 3.30 (t, J=4.5 Hz, 4H), 2.55 (s, 3H). MS m/z: 355 (M+H+).
The title compound was prepared as described in Example 124, except that 3-fluoro-2-iodo-4-(trifluoromethyl)aniline, which was also obtained as the other isomer in step 1, was substituted for 5-fluoro-2-iodo-4-(trifluoromethyl)aniline in step 2 of that route. 1H NMR (300 MHz, CD3OD) δ: 7.94 (t, J=8.4 Hz, 1H), 7.66 (d, J=8.7 Hz, 1H), 5.35 (d, J=14.4 Hz, 2H), 3.73-3.62 (m, 4H), 3.43-3.35 (m, 2H), 2.99 (s, 3H), 2.64 (s, 3H). MS m/z: 369 (M+H+).
The title compound was prepared as described in Example 122, except that 2-fluoro-4-(trifluoromethyl)aniline was substituted for 3-chloro-4-(trifluoromethyl)aniline in step 1 of that route. 1H NMR (300 MHz, D2O) δ: 7.68 (s, 1H), 7.49 (d, J=10.5 Hz, 1H), 4.97 (d, J=14.4 Hz, 2H), 3.65 (d, J=12.8 Hz, 2H), 3.55-3.46 (m, 2H), 3.30-3.22 (m, 2H), 2.92 (s, 3H), 2.46 (s, 3H). MS m/z: 369 (M+H+).
The title compound was prepared as described in Example 127, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, D2O) δ: 7.70 (s, 1H), 7.49 (d, J=10.5 Hz, 1H), 4.20 (br, 4H), 3.41 (br, 4H), 2.46 (s, 3H). MS m/z: 355 (M+H+).
The title compound was prepared as described in Example 122, except that 4-fluoro-3-(trifluoromethyl)aniline was substituted for 3-chloro-4-(trifluoromethyl)aniline in step 1 of that route. 1H NMR (300 MHz, D2O) δ: 7.61 (d, J=6.0 Hz, 1H), 7.37 (d, J=12.0 Hz, 1H), 4.76-4.68 (m, 2H), 3.65-3.23 (m, 6H), 2.91 (s, 3H), 2.45 (s, 3H). MS m/z: 369 (M+H+).
The title compound was prepared as described in Example 129, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, D2O) δ: 7.61 (d, J=6.0 Hz, 1H), 7.39 (d, J=12.0 Hz, 1H), 4.07-4.04 (m, 4H), 3.40-3.36 (m, 4H), 2.46 (s, 3H). MS m/z: 355 (M+H+).
The title compound was prepared as described in Example 122, except that 4-chloro-3-(trifluoromethyl)aniline was substituted for 3-chloro-4-(trifluoromethyl)aniline in step 1 of that route. 1H NMR (300 MHz, D2O) δ: 7.57 (s, 1H), 7.56 (s, 1H), 4.83 (d, J=14.4 Hz, 2H), 3.62 (d, J=12.8 Hz, 2H), 3.51-3.41 (m, 2H), 3.29-3.24 (m, 2H), 2.90 (s, 3H), 2.46 (s, 3H). MS m/z: 385 (M+H+).
The title compound was prepared as described in Example 131, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, D2O) δ: 7.60 (br, 2H), 4.11 (br, 4H), 3.40 (br, 4H), 2.47 (s, 3H). MS m/z: 371 (M+H+).
The title compound was prepared as described in Example 122, except that 4-(trifluoromethoxy)aniline was substituted for 3-chloro-4-(trifluoromethyl)aniline in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.19 (dd, J=2.4, 1.2 Hz, 1H), 7.88 (d, J=9.0 Hz, 1H), 7.72-7.68 (m, 1H), 5.17 (dd, J=14.1, 2.1 Hz, 2H), 3.72-3.58 (m, 4H), 3.46-3.42 (m, 2H), 2.99 (s, 3H), 2.65 (s, 3H). MS m/z: 367 (M+H+).
The title compound was prepared as described in Example 133, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 9.50 (br, 2H), 8.10 (d, J=0.6 Hz, 1H), 7.81 (d, J=9.3 Hz, 1H), 7.73 (dd, J=9.3, 0.6 Hz, 1H), 4.23 (t, J=5.1 Hz, 4H), 3.29 (br, 4H), 2.55 (s, 3H). MS m/z: 353 (M+H+).
The HCl salt of the title compound was prepared as described in Example 93, except that 2-amino-5-bromobenzonitrile was substituted for 2-amino-4,5-dichlorobenzonitrile in steps 2-5 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.31 (d, J=2.1 Hz, 1H), 7.88 (dd, J=8.7, 2.1 Hz, 1H), 7.65 (d, J=8.7 Hz, 1H), 5.18-5.13 (m, 2H), 3.70-3.58 (m, 4H), 3.43-3.39 (m, 2H), 2.98 (s, 3H), 2.63 (s, 3H). MS m/z: 361 (M+H+).
The HCl salt of the title compound was prepared as described in Example 135, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.42-8.40 (m, 1H), 7.88 (dd, J=8.7, 2.4 Hz, 1H), 7.67-7.64 (m, 1H), 4.32 (t, J=5.1 Hz, 4H), 3.49-3.31 (m, 4H), 2.64 (s, 3H). MS m/z: 347 (M+H+).
The HCl salt of the title compound was prepared as described in Example 88, except that 9-bromo-2-methyl-5-(4-methylpiperazin-1-yl)-[1,2,4]triazolo[1,5-c]quinazoline was substituted for 8-bromo-4-(4-methylpiperazin-1-yl)-[1,2,4]triazolo[4,3-a]quinoxaline, in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.27 (d, J=1.8 Hz, 1H), 8.02 (dd, J=8.7, 2.1 Hz, 1H), 7.80 (d, J=8.4 Hz, 1H), 6.92 (dd, J=17.7, 11.1 Hz, 1H), 5.99 (d, J=17.4 Hz, 1H), 5.44 (d, J=11.4 Hz, 1H), 5.10-5.05 (m, 2H), 3.73-3.66 (m, 4H), 3.45-3.37 (m, 2H), 2.99 (s, 3H), 2.71 (s, 3H). MS m/z: 309 (M+H+).
The HCl salt of the title compound was prepared as described in Example 89, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.28 (d, J=1.8 Hz, 1H), 8.01 (dd, J=8.4, 2.1 Hz, 1H), 7.79 (d, J=8.4 Hz, 1H), 6.92 (dd, J=17.7, 11.1 Hz, 1H), 5.98 (d, J=17.4 Hz, 1H), 5.44 (d, J=10.8 Hz, 1H), 4.31 (t, J=5.1 Hz, 4H), 3.49 (t, J=5.1 Hz, 4H), 2.70 (s, 3H). MS m/z: 295 (M+H+).
The HCl salt of the title compound was prepared as described in Example 90, except that 2-methyl-5-(4-methylpiperazin-1-yl)-9-vinyl-[1,2,4]triazolo[1,5-c]quinazoline was substituted for 4-(4-methylpiperazin-1-yl)-8-vinyl-[1,2,4]triazolo[4,3-a]quinoxaline, in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.14 (s, 1H), 7.80 (m, 2H), 5.05-5.00 (m, 2H), 3.72-3.58 (m, 4H), 3.46-3.37 (m, 2H), 2.99 (s, 3H), 2.88 (q, J=7.8 Hz, 2H), 2.71 (s, 3H), 1.35 (t, J=7.8 Hz, 3H). MS m/z: 311 (M+H+).
The HCl salt of the title compound was prepared as described in Example 91, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.15 (s, 1H), 7.83 (m, 2H), 4.29 (t, J=4.8 Hz, 4H), 3.49 (t, J=5.1 Hz, 4H), 2.89 (q, J=7.5 Hz, 2H), 2.85 (s, 3H), 1.35 (t, J=7.8 Hz, 3H). MS m/z: 297 (M+H+).
A 500 mL 3-necked round bottom flask was charged with 2-amino-5-chlorobenzoic acid (17 g, 0.1 mol) and 1,2-dichloroethane (200 mL). To the above was added dropwise a solution of triphosgene (21 g, 0.21 mol) in 1,2-dichloroethane (100 mL) at 80° C. The resulting mixture was heated at 80° C. for further 3 h then cooled in ice-water. The precipitate was collected by filtration and dried to afford 19 g (97%) of the product as white solid. 1H NMR (300 MHz, DMSO-d6) δ: 11.85 (br, 1H), 7.88 (d, J=2.4 Hz, 1H), 7.78 (dd, J=8.7, 2.4 Hz, 1H), 7.15 (d, J=8.7 Hz, 1H).
A 500 mL 3-necked round bottom flask was charged with ethyl nitroacetate (16 mL, 144 mmol), Et3N (20 mL, 144 mmol) and anhydrous THF (400 mL). To the above was added dropwise a solution of 6-chloro-1H-benzo[d]1,3-oxazine-2,4-dione (19 g, 96 mmol) in THF (100 mL). The resulting solution was heated at 55° C. overnight then concentrated under reduced pressure. The residue was washed with Et2O then dissolved in water and acidified with 6 M HCl. The precipitate was collected by filtration and dried to afford 8 g (34%) of the product as yellow solid. 1H NMR (300 MHz, DMSO-d6) δ: 11.85 (br, 1H), 8.00 (d, J=2.7 Hz, 1H), 7.64 (dd, J=8.4, 2.1 Hz, 1H), 7.31 (d, J=9.0 Hz, 1H).
A 250 mL round bottom flask was charged with 6-chloro-4-hydroxy-3-nitrohydroquinolin-2-one (2.4 g, 10 mmol) and 1 M NaOH aqueous solution (100 mL). To the above was added Na2S2O4 (12 g, 59 mmol) portion-wise. The resulting solution was stirred in the dark for 30 min. It was then cooled to 0° C. and acidified with 6 M HCl. The precipitate was collected by filtration, washed with small amount of acetone, and dried, to afford 2 g (83%) of the product as white solid. 1H NMR (300 MHz, DMSO-d6) δ: 12.06 (br, 1H), 8.04 (d, J=2.4 Hz, 1H), 7.54 (dd, J=9.3, 2.4 Hz, 1H), 7.35 (d, J=8.7 Hz, 1H), 5.0 (br, 3H). MS m/z: 211 (M+H+).
A 100 mL round bottom flask was charged with 3-amino-6-chloro-4-hydroxyhydroquinolin-2-one hydrochloride salt (2 g, 8.1 mmol) and triethylorthoformate (30 mL). The resulting solution was heated at reflux for 30 min then cooled in ice-water. The precipitate was collected by filtration, washed with CH2Cl2, and dried, to afford 1.5 g (84%) of the product as yellow solid. 1H NMR (300 MHz, DMSO-d6) δ: 12.15 (br, 1H), 8.87 (s, 1H), 7.96 (d, J=2.1 Hz, 1H), 7.62 (dd, J=8.7, 2.1 Hz, 1H), 7.50 (d, J=8.4 Hz, 1H). MS m/z: 221 (M+H+).
A 100 mL round bottom flask was charged with 8-chloro-5-hydro-1,3-oxazolo[4,5-c]quinolin-4-one (1.7 g, 7.7 mmol) and POCl3 (20 mL). The resulting solution was heated at reflux for 20 min then concentrated in vacuo. The residue was mixed with saturated aqueous Na2CO3 and extracted with CH2Cl2. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. It was further purified by flash column chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 480 mg (26%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 9.19 (s, 1H), 8.38 (dd, J=2.4, 0.3 Hz, 1H), 8.15 (dd, J=9.0, 0.3 Hz, 1H), 7.91 (dd, J=8.7, 2.4 Hz, 1H). MS m/z: 239 (M+H+).
A 20 mL microwave reaction tube was charged with 4,8-dichlorooxazolo[4,5-c]quinoline (320 mg, 1.3 mmol), N-methylpiperazine (0.16 mL, 1.4 mmol), Et3N (0.6 mL, 4.3 mmol) and anhydrous EtOH (15 mL). The resulting solution was heated at 130° C. for 1 h in a Biotage microwave reactor. The solvent was evaporated and the residue was purified by flash column chromatography on silica gel with 10% MeOH in CH2Cl2, to afford 100 mg (25%) of the product as white solid. 1H NMR (300 MHz, CD3OD) δ: 8.51 (s, 1H), 7.94 (d, J=2.7 Hz, 1H), 7.69 (d, J=9.0 Hz, 1H), 7.49 (dd, J=9.0, 2.7 Hz, 1H), 4.26 (t, J=5.1 Hz, 4H), 2.65 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared as described in Example 141, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.60 (s, 1H), 8.05 (d, J=2.4 Hz, 1H), 7.78 (d, J=9.0 Hz, 1H), 7.58 (dd, J=9.0, 2.4 Hz, 1H), 4.47 (t, J=5.4 Hz, 4H), 3.36 (t, J=5.4 Hz, 4H). MS m/z: 289 (M+H+).
A 500 mL round bottom flask was charged with 3-amino-6-chloro-4-hydroxyhydroquinolin-2-one hydrochloride salt (prepared in Example 141 step 1-3, 6.8 g, 28 mmol) and anhydrous THF (150 mL). To the above were added dropwise anhydrous Et3N (9.6 mL, 69 mmol) and acetyl chloride (3 mL, 42 mmol). The resulting solution was heated at reflux for 6 h, cooled to room temperature, diluted with H2O and acidified with 6N HCl. The precipitate was collected by filtration and washed with H2O, to afford 6 g (86%) of the product as yellow solid. 1H NMR (300 MHz, DMSO-d6) δ: 12.07 (br, 1H), 11.94 (br, 1H), 9.76 (br, 1H), 7.79 (d, J=2.7 Hz, 1H), 7.54 (dd, J=8.7, 2.4 Hz, 1H), 7.29 (d, J=8.7 Hz, 1H), 2.23 (s, 3H).
A 500 mL round bottom flask was charged with N-(6-chloro-4-hydroxy-2-oxo-3-hydroquinolyl)acetamide (3 g, 12 mmol) and xylene (250 mL). The resulting solution was heated at 190° C. for 4 h. The solvent was evaporated under reduced pressure and the residue was re-dissolved in EtOAc and washed with H2O. The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 1 g (36%) of the product which was used as such in the next step. 1H NMR (300 MHz, DMSO-d6) δ: 12.06 (br, 1H), 7.89 (d, J=2.1 Hz, 1H), 7.59 (dd, J=9.0, 2.4 Hz, 1H), 7.48 (d, J=9.0 Hz, 1H), 2.65 (s, 3H).
A 50 mL round bottom flask was charged with 8-chloro-2-methyloxazolo[4,5-c]quinolin-4(5H)-one (1.0 g, 4.3 mmol) and POCl3 (20 mL). The resulting solution was heated at reflux for 20 min. After evaporation of the solvent, the residue was poured into saturated aqueous Na2CO3 and extracted with CH2Cl2. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 730 mg (68%) of the product as white solid. MS m/z: 328 (M+H+).
A 20 mL microwave reaction tube was charged with 4,8-dichloro-2-methyloxazolo[4,5-c]quinoline (300 mg, 1.2 mmol), N-methylpiperazine (0.16 mL, 1.4 mmol), Et3N (0.31 ml, 2.2 mmol) and anhydrous EtOH (15 mL). The resulting solution was heated at 100° C. for 1 h in a Biotage microwave reactor. The solvent was evaporated and the residue was purified by flash column chromatography on silica gel with 10% MeOH in CH2Cl2, to afford 110 mg (29%) of the product as white solid. 1H NMR (300 MHz, CD3OD) δ: 7.81 (d, J=2.4 Hz, 1H), 7.63 (d, J=8.7 Hz, 1H), 7.44 (dd, J=9.0, 2.4 Hz, 1H), 4.19 (t, J=4.5 Hz, 4H), 2.67 (s, 3H), 2.60 (t, J=4.8 Hz, 4H), 2.35 (s, 3H). MS m/z: 316 (M+H+).
The title compound was prepared as described in Example 143, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 7.87 (d, J=2.7 Hz, 1H), 7.65 (d, J=9.0 Hz, 1H), 7.46 (dd, J=9.0, 2.4 Hz, 1H), 4.16 (t, J=5.4 Hz, 4H), 2.97 (t, J=5.1 Hz, 4H), 2.69 (s, 3H). MS m/z: 302 (M+H+).
The title compound was prepared as described in Example 141, except that 2-amino-4,5-difluorobenzoic acid was substituted for 2-amino-5-chlorobenzoic acid in step 1, and ethyl orthoacetate was substituted for ethyl orthoformate in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 7.65-7.63 (m, 1H), 7.45-7.43 (m, 1H), 4.18 (t, J=4.8 Hz, 4H), 2.67 (s, 3H), 2.59 (t, J=5.1 Hz, 4H), 2.35 (s, 3H). MS m/z: 319 (M+H+).
The title compound was prepared as described in Example 145, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 7.87-7.85 (m, 1H), 7.56-7.54 (m, 1H), 4.04 (t, J=4.8 Hz, 4H), 2.82 (t, J=5.1 Hz, 4H), 2.69 (s, 3H). MS m/z: 305 (M+H+).
A 100 mL round bottom flask was charged with furan-2-carboxylic acid (1.0 g, 7.8 mmol) and SOCl2 (15 mL). The resulting mixture was stirred at reflux for 2.5 h then concentrated in vacuo. The residue was dissolved in CH2Cl2 (10 mL) and to the solution was added dropwise a solution of 4-chloro-2-iodophenylamine (1.8 g, 7.1 mmol) and Et3N (1.3 mL, 9.2 mmol) in CH2Cl2 (20 mL) at 0° C. The resulting solution was stirred at room temperature for 18 h, then diluted with CH2Cl2 (200 mL) and washed with H2O (100 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 4% EtOAc in petroleum ether, to afford 2.0 g (71%) of the product. MS m/z: 347 (M+H+).
A 100 mL round bottom flask was charged with N-(4-chloro-2-iodophenyl)furan-2-carboxamide (3.70 g, 10.6 mmol), 4-dimethylaminopyridine (1.30 g, 10.6 mmol) and DMF (30 mL). To the above was added dropwise a solution of di-tert-butyl dicarbonate (7.0 g, 31.8 mmol) in DMF (10 mL) at 0° C. The resulting solution was stirred at 60° C. for 18 h then cooled to room temperature. It was diluted with H2O (100 mL) and extracted with EtOAc (100 mL×3). The combined organic layers were washed with brine (100 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a 1:16 EtOAc/Petroleum ether, to give 2.50 g (53%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 7.90 (d, J=2.3 Hz, 1H), 7.56 (dd, J=1.8, 0.8 Hz, 1H), 7.38 (dd, J=8.3, 2.3 Hz, 1H), 7.20 (d, J=8.3 Hz, 1H), 7.14 (dd, J=3.5, 0.8 Hz, 1H), 6.54 (dd, J=3.5, 1.8 Hz, 1H), 1.40 (s, 9H).
A 20 mL microwave reaction tube was charged with tert-butyl 4-chloro-2-iodophenyl(furan-2-carbonyl)carbamate (0.45 g, 1.0 mmol), palladium(II) acetate (0.023 g, 0.1 mmol), tricyclohexylphosphine (0.028 g, 0.1 mmol), K2CO3 (0.28 g, 2.0 mmol) and N,N-dimethylacetamide (10 mL). After the air was purged by bubbling argon into the reaction solution, the tube was sealed and heated at 140° C. for 1 h in a Biotage microwave reactor. It was diluted with H2O (100 mL) and extracted with EtOAc (100 mL×2). The combined organic layers were washed with brine (100 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 20-100% EtOAc in petroleum ether, to afford 0.10 g (53%) of the product as white solid.
A 100 mL round bottom flask was charged with 8-chlorofuro[2,3-c]quinolin-4(5H)-one (100 mg, 0.46 mmol) and POCl3 (20 mL). The resulting solution was heated at reflux for 2 h then concentrated under reduced pressure. The residue was mixed with saturated aqueous Na2CO3 and extracted with EtOAc (50 mL×4). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The resulting solid was washed with EtOH to afford 100 mg (93%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 8.10-8.05 (m, 2H), 7.95 (d, J=2.0 Hz, 1H), 7.65 (dd, J=9.1, 2.1 Hz, 1H), 7.30 (d, J=2.1 Hz, 1H).
A 20 mL microwave reaction tube was charged with 4,8-dichlorofurano[2,3-c]quinoline (110 mg, 0.46 mmol), N-methylpiperazine (0.15 mL, 1.4 mmol) and anhydrous iPrOH (10 mL). The resulting solution was heated at 130° C. for 1 h in a Biotage microwave reactor. The solvent was evaporated and the residue was purified by flash column chromatography on silica gel with 10% MeOH in CH2Cl2 to afford 100 mg (72%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 7.85 (d, J=2.4 Hz, 1H), 7.75 (m, 2H), 7.53 (dd, J=6.3, 2.4 Hz, 1H), 7.13 (d, J=1.8 Hz, 1H), 4.06 (t, J=5.1 Hz, 4H), 2.61 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 302 (M+H+).
The title compound was prepared as described in Example 147, except that piperazine was substituted for N-methylpiperazine in step 5 of that route. 1H NMR (300 MHz, D2O) δ: 8.14 (d, J=1.5 Hz, 1H), 8.00 (s, 1H), 7.73 (d, J=9.0 Hz, 1H), 7.59 (m, 1H), 7.35 (s, 1H), 4.31 (t, J=5.1 Hz, 4H), 3.48 (t, J=5.1 Hz, 4H). MS m/z: 288 (M+H+).
The title compound was prepared as described in Example 147, except that thiophene-2-carboxylic acid was substituted for furan-2-carboxylic acid in step 1 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.07 (d, J=2.1 Hz, 1H), 7.83 (m, 2H), 7.73 (d, J=5.4 Hz, 1H), 7.50 (m, 1H), 3.85 (t, J=5.1 Hz, 4H), 2.66 (t, J=4.8 Hz, 4H), 2.40 (s, 3H). MS m/z: 318 (M+H+).
A 500 mL 3-necked round bottom flask was charged with 5-chloroindole (15.2 g, 0.10 mol), pyridine (10.5 mL) and anhydrous ethyl ether (200 mL). To the above was added dropwise a solution of ethyl oxalylchloride (16.4 g, 0.12 mol) in anhydrous ethyl ether (50 mL) at 0-5° C. The resulting mixture was stirred at 0° C. for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1, Rf=0.3). Work-up: the mixture was concentrated in vacuo. The resulting solid was washed with a small amount of ethyl ether, then with water, and dried, to give 19.3 g (77%) of the product. MS m/z: 252 (M+H+).
A 250 mL round bottom flask was charged with ethyl 2-(5-chloro-1H-indol-3-yl)-2-oxoacetate (3 g, 12 mmol), methylhydrazine hydrochloride salt (3 g, 16 mmol), absolute ethanol (150 mL) and acetic acid (3 mL). The resulting mixture was heated at reflux for 24 h. Work-up: the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel with a 1:40 MeOH/CH2Cl2, to give 2.2 g (79%) of the product. 1H NMR (300 MHz, DMSO-d6) δ: 11.43 (s, 1H), 8.68 (s, 1H), 7.99 (s, 1H), 7.39-7.30 (m, 2H), 4.12 (s, 3H). MS m/z: 234 (M+H+).
A 100 mL round bottom flask was charged with 8-chloro-2-methyl-2H-pyrazolo[3,4-c]quinolin-4(5H)-one (2.2 g, 9.4 mmol), PCl5 (0.28 g, 1.9 mmol) and POCl3 (40 mL). The resulting mixture was heated at reflux for 2 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10, Rf=0.3). Work-up: POCl3 was evaporated under reduced pressure. The residue was carefully poured into ice-cooled saturated aqueous NaHCO3 (100 mL) and extracted with CH2Cl2 (50 mL×4). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a 1:4 EtOAC/Petroleum ether, to give 1.67 g (70%) of the product. MS m/z: 253 (M+H+).
A 100 mL round bottom flask was charged with 4,8-dichloro-2-methyl-2H-pyrazolo[3,4-c]quinoline (0.504 g, 2 mmol), N-methylpiperazine (0.6 g, 6 mmol), Et3N (0.84 mL, 6.1 mmol) and absolute ethanol (35 mL). The resulting mixture was heated at reflux for 24 h. Work-up: the reaction mixture was concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel with a 1:20 MeOH/CH2Cl2, to give 300 mg (47%) of the product. 1H NMR (300 MHz, CD3OD) δ: 8.44 (s, 1H), 7.84 (d, J=2.7 Hz, 1H), 7.54 (d, J=8.7 Hz, 1H), 7.30 (dd, J=8.7, 2.4 Hz, 1H), 4.36 (br, 4H), 4.18 (s, 3H), 2.91 (t, J=5.1 Hz, 4H), 2.57 (s, 3H). MS m/z: 316 (M+H+).
The HCl salt of the title compound was prepared as described in Example 150, except that tert-butyl piperazine-1-carboxylate was substituted for N-methylpiperazine in step 4 of that route. The resulting tert-butyl 4-(8-chloro-2-methyl-2H-pyrazolo[3,4-c]quinolin-4-yl)piperazine-1-carboxylate was treated with 3 M HCl in methanol solution overnight at room temperature. The solid was collected by filtration, washed with methanol, and dried, to afford the HCl salt of the title compound as white solid. 1H NMR (300 MHz, DMSO-d6) δ: 9.83 (br, 2H), 9.04 (s, 1H), 8.35 (m, 1H), 8.22 (d, J=2.1 Hz, 1H), 7.57 (dd, J=8.7, 2.1 Hz, 1H), 4.72 (br, 4H), 4.22 (s, 3H), 3.78 (m, 4H). MS m/z: 288 (M+H+).
A 500 mL 3-necked round bottom flask was charged with hydrazine hydrate (40 g, 0.80 mol) and EtOH (280 mL). To the above solution was added dropwise a solution of 4-methoxybenzylchloride (12.5 g, 0.080 mol) in EtOH (30 mL) at room temperature. The resulting mixture was stirred at 90° C. for 2 h. Work-up: the reaction mixture was concentrated in vacuo then re-dissolved in EtOH (150 mL). The solution was acidified with 5 M HCl (120 mL) at 0° C. The resulting precipitate was collected by filtration and dried to afford 8.72 g (72%) of the product as white solid. MS m/z: 153 (M+H+).
The title compound was prepared as described in Example 150, except that (4-methoxybenzyl)hydrazine HCl salt was substituted for methylhydrazine HCl salt in step 2 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 11.43 (s, 1H), 8.77 (s, 1H), 8.01 (d, J=2.1 Hz, 1H), 7.38-7.29 (m, 4H), 6.96-6.93 (m, 2H), 5.52 (s, 2H), 3.74 (s, 3H). MS m/z: 340 (M+H+).
The title compound was prepared as described in Example 150, except that 8-chloro-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-c]quinolin-4(5H)-one was substituted for 8-chloro-2-methyl-2H-pyrazolo[3,4-c]quinolin-4(5H)-one in step 3 of that route. MS m/z: 359 (M+H+).
The title compound was prepared as described in Example 150, except that 4,8-dichloro-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-c]quinoline was substituted for 4,8-dichloro-2-methyl-2H-pyrazolo[3,4-c]quinoline in step 4 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.20 (s, 1H), 7.83 (s, 1H), 7.52 (m, 1H), 7.38-7.22 (m, 3H), 6.88 (m, 2H), 5.52 (s, 2H), 4.29 (m, 4H), 3.74 (s, 3H), 2.66 (m, 4H), 2.38 (s, 3H). MS m/z: 422 (M+H+).
A 50 mL 3-necked round bottom flask was charged with 8-chloro-2-(4-methoxybenzyl)-4-(4-methylpiperazin-1-yl)-2H-pyrazolo[3,4-c]quinoline (1.28 g, 3.0 mmol), trifluoroacetic acid (30 mL), anisole (881 mg, 8.2 mmol) and concentrated H2SO4 (0.45 mL). The resulting mixture was stirred at 0° C. for 2 h and then at 50° C. overnight. Work-up: the reaction solution was added dropwise to an ice-cooled saturated aqueous Na2CO3 (100 mL) and extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a 1:20 MeOH/CH2Cl2, to afford 400 mg (44%) of the product. 1H NMR (300 MHz, CD3OD) δ: 8.57 (s, 1H), 7.97 (d, J=2.1 Hz, 1H), 7.60 (d, J=8.7 Hz, 1H), 7.33 (dd, J=8.7, 2.4 Hz, 1H), 4.22 (m, 4H), 2.64 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 302 (M+H+).
The title compound was prepared as described in Example 152, except that tert-butyl piperazine-1-carboxylate was substituted for N-methylpiperazine in step 5 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.93 (s, 1H). 8.24 (d, J=2.1 Hz, 1H), 8.00 (d, J=9.0 Hz, 1H), 7.60 (dd, J=8.7, 2.1 Hz, 1H), 3.62 (m, 4H), 3.30 (m, 4H). MS m/z: 288 (M+H+).
A 25 mL 3-necked round bottom flask was charged with 8-chloro-4-(4-methylpiperazin-1-yl)-2H-pyrazolo[3,4-c]quinoline (152, 200 mg, 0.664 mmol) and KOH (372 mg, 6.64 mmol) and H2O (10 mL). To the above was added dropwise a solution of dimethyl sulfate (418 mg, 3.32 mmol) in acetone (2 mL). The resulting mixture was stirred at room temperature for 0.5 h. Reaction progress was monitored by TLC (MeOH/CH2Cl2=10:1, Rf=0.3). Work-up: the reaction mixture was concentrated under reduced pressure and the residue was purified by preparative HPLC to give 100 mg (46%) of the product. 1H NMR (300 MHz, DMSO-d6) δ: 8.91 (s, 1H), 8.12 (d, J=2.1 Hz, 1H), 7.60 (d, J=8.7 Hz, 1H), 7.42 (dd, J=8.7, 2.4 Hz, 1H), 4.55 (br, 4H), 4.22 (s, 3H), 3.60 (m., 4H), 3.24 (s, 6H). MS m/z: 330 (M+H+).
The title compound was prepared as described in Example 150, except that 5-trifluoromethylindole was substituted for 5-chloroindole in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.57 (s, 1H), 8.18 (s, 1H), 7.67 (d, J=9.0 Hz, 1H), 7.55 (d, J=9.0 Hz, 1H), 4.36-4.32 (m, 4H), 4.21 (s, 3H), 2.64-2.61 (m, 4H), 2.36 (s, 3H). MS m/z: 350 (M+H+).
The title compound was prepared as described in Example 155, except that piperazine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.98 (s, 1H), 8.51 (s, 1H), 8.18 (d, J=9.0 Hz, 1H), 7.88 (d, J=9.0 Hz, 1H), 4.34 (s, 3H), 3.66-3.63 (m, 4H), 3.31-3.29 (m, 4H). MS m/z: 336 (M+H+).
The HCl salt of the title compound was prepared as described in Example 152.
A 500 mL 3-necked round bottom flask was charged with 4-(trifluoromethyl)aniline (22.5 g, 0.14 mol) and MeOH (100 mL). To the above was added dropwise a solution of IC1 (25 g, 0.15 mol) in CH2Cl2 (100 mL) at 0° C. The resulting mixture was stirred at room temperature for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10, Rf=0.5). Work-up: the mixture was concentrated in vacuo. The residue was re-dissolved in CH2Cl2, washed with water, dried over anhydrous Na2SO4 and concentrated in vacuo, to give 37.8 g (97%) of the product. 1H NMR (300 MHz, CDCl3) δ: 7.86 (d, J=1.2 Hz, 1H), 7.36 (dd, J=8.4, 1.8 Hz, 1H), 6.73 (d, J=8.7 Hz, 1H), 4.41 (br, 2H).
A 500 mL 3-necked round bottom flask was charged with 2-iodo-4-(trifluoromethyl)aniline (63 g, 0.22 mol) and pyridine (300 mL). To the above was added dropwise ethyl chloroformate (36 g, 0.33 mol) at 0° C. The resulting mixture was stirred at room temperature for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:20, Rf=0.5). Work-up: the mixture was concentrated in vacuo. The residue was re-dissolved in CH2Cl2, washed with saturated NH4Cl, dried over anhydrous Na2SO4 and concentrated in vacuo, to give 43.5 g (55%) of the product. MS m/z: 358 (M−H+).
A 250 mL 3-necked round bottom flask was charged with ethoxy-N-[2-iodo-4-(trifluoromethyl)phenyl]carboxamide (50 g, 0.14 mol), CuI (1.5 g, 7.87 mmol), (1,1′-bis(diphenylphosphino)ferrocene)dichloropalladium(II) (5.0 g, 7.2 mmol), Et3N (200 mL) and THF (400 mL). To the above was added dropwise 2,2-dimethyl-2-silabut-3-yne (21.7 mL, 0.15 mol). The resulting mixture was stirred at room temperature for 0.5 h under N2 atmosphere. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:20). Work-up: the mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 5% EtOAc in petroleum ether, to afford 31.5 g (74%) of the product. 1H NMR (300 MHz, DMSO-d6) δ: 8.28 (d, J=8.7 Hz, 1H), 7.64 (m, 1H), 7.55 (m, 2H), 4.26 (q, J=6.9 Hz, 2H), 1.34 (t, J=7.2 Hz, 3H), 0.31 (s, 9H).
A 250 mL 3-necked round bottom flask was charged with N-[2-(3,3-dimethyl-3-silabut-1-ynyl)-4-(trifluoromethyl)phenyl]ethoxycarboxamide (31.5 g, 0.1 mol), EtONa (32.5 g, 0.48 mol) and ethanol (200 mL). The resulting mixture was heated at reflux for 2 h. Work-up: the mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 25% EtOAc in petroleum ether, to afford 14 g (77%) of the product. 1H NMR (300 MHz, DMSO-d6) δ: 8.36 (s, 1H), 7.96-7.94 (m, 1H), 7.46-7.44 (m, 2H), 7.32-7.30 (m, 1H), 6.66-6.64 (m, 1H).
The HCl salt of the title compound was prepared as described in Example 152, except that 5-(trifluoromethyl)indole was substituted for 5-chloroindole in step 2 of that route. 1H NMR (300 MHz, D2O) δ: 8.52-8.50 (m, 1H), 8.12-8.10 (m, 1H), 7.72-7.69 (m, 1H), 7.62-7.59 (m, 1H), 5.38-5.35 (m, 2H), 3.74-3.71 (m, 4H), 3.32-3.28 (m, 2H), 2.87 (s, 3H). MS m/z: 336 (M+H+).
A 100 mL round bottom flask was charged with NaOH (2.33 g, 0.058 mol) and H2O (10 mL). To the above was added dropwise nitromethane (3.1 mL, 3.56 g, 0.058 mol) at room temperature. The resulting solution was slowly warmed to 45° C. for 5 min then cooled to 0° C. and acidified with concentrated HCl. It was added to a suspension of 2-amino-5-chlorobenzoic acid (5.0 g, 0.029 mol) in concentrated HCl (50 mL) and H2O (20 mL). The reaction solution was allowed to stand overnight at room temperature. The solid was collected by filtration, washed with H2O, and dried, to afford 4.7 g (66%) of the product.
A 500 mL round bottom flask was charged with 5-chloro-2-(2-nitroethylideneamino)benzoic acid (25 g, 0.10 mol), K2CO3 (42.6 g, 0.30 mol) and acetic anhydride (250 mL). The resulting mixture was heated to 90° C. for 1 h. Work-up: the resulting solid was collected by filtration, washed with water and dried to give 17.5 g (76%) of the product as grey solid. 1H NMR (300 MHz, DMSO-d6) δ: 9.12 (s, 1H), 8.15 (s, 1H), 7.72 (s, 2H). MS m/z: 224 (M+H+).
A 500 mL round bottom flask was charged with 6-chloro-3-nitroquinolin-4-ol (2.41 g, 10.8 mmol), acetonitrile (50 mL), N,N-diisopropylethylamine (2.49 g, 21.6 mmol) and POCl3 (1.5 mL, 16.2 mmol). The resulting solution was heated at reflux for 1 h. Work-up: the solvent was removed, and the residue was purified by flash column chromatography on silica gel with a 1:15 EtOAc/Petroleum ether, to give 2.0 g (77%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 9.23 (s, 1H), 8.40 (d, J=2.1 Hz, 1H), 8.16 (d, J=9.0 Hz, 1H), 7.89 (dd, J=9.0, 2.4 Hz, 1H).
A 100 mL round bottom flask was charged with 4,6-dichloro-3-nitroquinoline (2.0 g, 8.3 mmol) and THF (50 mL). To the above was added methylamine (2 M in THF, 6.2 mL) at 0° C. The resulting solution was stirred at room temperature for 1 h. Work-up: the solvent was removed. The residue was dissolved in CH2Cl2 (300 mL) and washed with water (50 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. It was further purified by flash column chromatography on silica gel with a 1:2:2 EtOAc/Petroleum ether/CH2Cl2, to give 1.8 g (91%) of the product as yellow solid. MS m/z: 238 (M+H+).
A 100 mL round bottom flask was charged with 6-chloro-N-methyl-3-nitroquinolin-4-amine (1.1 g, 4.6 mmol), sodium dithionite (1.62 g, 9.2 mmol), water (10 mL) and EtOH (50 mL). The resulting mixture was heated at reflux for 1 h. Work-up: the solvent was removed and the residue was washed with water (5 mL) and dried to afford 0.96 g (quantitative) of the product, which was used as such for the next step. MS m/z: 208 (M+H+).
A 100 mL round bottom flask was charged with 6-chloro-N4-methylquinoline-3,4-diamine (0.96 g, 4.6 mmol), HCOOH (30 mL) and concentrated HCl (5 mL). The resulting mixture was heated at reflux for 30 min. Work-up: the solvent was removed. The residue was poured into 50% aqueous NaOH at 0° C. and extracted with CH2Cl2 (100 mL×4). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. It was further purified by flash column chromatography on silica gel with 33% EtOAc in petroleum ether then 3% MeOH in CH2Cl2, to give 0.47 g (46%) of the product as white solid. 1H NMR (300 MHz, CDCl3) δ: 9.30 (s, 1H), 8.23 (d, J=4.2 Hz, 1H), 8.19 (s, 1H), 7.94 (s, 1H), 7.63 (d, J=6.6 Hz, 1H), 4.28 (s, 3H). MS m/z: 218 (M+H+).
A 50 mL round bottom flask was charged with 8-chloro-1-methyl-1H-imidazo[4,5-c]quinoline (1.4 g, 6.46 mmol), 30% H2O2 (1.5 mL) and acetic acid (20 mL). The reaction mixture was stirred at 80° C. overnight then concentrated under reduced pressure. The residue was neutralized with saturated aqueous NaHCO3 and the resulting precipitate was collected by filtration and dried. It was re-suspended in acetic anhydride (15 mL) and heated at reflux for 1 h. The solvent was removed and methanol (10 mL) was added to the residue, followed by dropwise addition of a solution of 28% sodium methoxide in methanol until PH 10. The solid was collected by filtration and dried to give 0.40 g (27%) of the product as yellow solid. 1H NMR (300 MHz, DMSO-d6) δ: 11.70 (s, 1H), 8.12 (s, 1H), 8.05 (s, 1H), 7.53-7.44 (m, 2H), 4.17 (s, 3H). MS m/z: 234 (M+H+).
A 50 mL round bottom flask was charged with 8-chloro-1-methyl-1H-imidazo[4,5-c]quinolin-4(5H)-one (0.20 g, 0.86 mmol) and POCl3 (5 mL). The mixture was heated at reflux for 1 h. Work-up: the solvent was removed under reduced pressure. The residue was treated with saturated aqueous Na2CO3 at 0° C., extracted with CH2Cl2 (50 mL×2), concentrated in vacuo and further purified by flash column chromatography on silica gel with 5% MeOH in CH2Cl2, to give 0.12 g (56%) of the product as yellow solid. MS m/z: 252 (M+H+).
A 20 mL microwave reaction tube was charged with 4,8-dichloro-1-methyl-1H-imidazo[4,5-c]quinoline (0.21 g, 0.84 mmol), piperazine (0.14 g, 1.68 mmol) and EtOH (10 mL). The resulting mixture was heated at 140° C. for 2 h in a Biotage microwave reactor. Work-up: the solvent was removed. The residue was diluted with CH2Cl2 (50 mL) and washed with water (30 mL×2). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was then treated with 3 M HCl (2.0 mL) and THF (20 mL). The resulting white solid was collected by filtration and dried, to give 160 mg (57%) of the HCl salt of the product as white solid. 1H NMR (300 MHz, D2O) δ: 8.17 (s, 1H), 7.93 (d, J=2.1 Hz, 1H), 7.70 (d, J=9.3 Hz, 1H), 7.44 (dd, J=9.0, 2.1 Hz, 1H), 4.53 (t, J=5.4 Hz, 4H), 4.03 (s, 3H), 3.50 (t, J=5.4 Hz, 4H). MS m/z: 302 (M+H+).
The title compound was prepared as described in Example 158, except that N-methylpiperazine was substituted for piperazine in step 9 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.32 (s, 1H), 8.22 (d, J=2.1 Hz, 1H), 7.73 (d, J=8.7 Hz, 1H), 7.54 (dd, J=9.0, 2.1 Hz, 1H), 4.26 (s, 3H), 3.26 (br, 8H), 2.75 (s, 3H). MS m/z: 316 (M+H+).
The title compound was prepared as described in Example 158, except that 2,4-dimethoxybenzylamine was substituted for methylamine in step 4 of that route. MS m/z: 373 (M+H+).
The title compound was prepared as described in Example 158, except that 6-chloro-N-(2,4-dimethoxybenzyl)-3-nitroquinolin-4-amine was substituted for 6-chloro-N-methyl-3-nitroquinolin-4-amine in step 5 of that route.
The title compound was prepared as described in Example 158, except that 6-chloro-N4-(2,4-dimethoxybenzyl)quinoline-3,4-diamine was substituted for 6-chloro-N4-methylquinoline-3,4-diamine, and methyl orthoformate for HCOOH and concentrated HCl in step 6 of that route.
A 100 mL round bottom flask was charged with 8-chloro-1-(2,4-dimethoxybenzyl)-1H-imidazo[4,5-c]quinoline (2.10 g, 5.94 mmol), 3-chloroperbenzoic acid (1.23 g, 7.13 mmol) and CH2Cl2 (50 mL). The resulting solution was stirred at room temperature for 3 h. Reaction progress was monitored by TLC (MeOH/CH2Cl2=1:20, Rf=0.4). Work-up: the mixture was concentrated and the residue was purified by flash column chromatography on silica gel with a 1:20 MeOH/CH2Cl2, to give 1.7 g (77%) of white solid, which was suspended in acetic anhydride (20 mL) and stirred at reflux for 1 h. The mixture was concentrated and the residue was diluted with methanol (5 mL), followed by dropwise addition of a solution of 28% sodium methoxide in methanol until PH 10. The solid was collected by filtration and dried to give 1.5 (68%) of the product as white solid. 1H NMR (300 MHz, DMSO-d6) δ: 8.17 (s, 1H), 7.60 (s, 1H), 7.34 (d, J=8.1 Hz, 1H), 7.25 (d, J=7.8 Hz, 1H), 6.68 (s, 1H), 6.53 (d, J=8.4 Hz, 1H), 6.40 (d, J=9.0 Hz, 1H), 5.61 (s, 2H), 3.94 (s, 3H), 3.71 (s, 3H).
A 50 mL round bottom flask was charged with 8-chloro-1-(2,4-dimethoxybenzyl)-1H-imidazo[4,5-c]quinolin-4(5H)-one (0.80 g, 2.17 mmol), POCl3 (15 mL) and N,N-diisopropylethylamine (0.50 g, 4.34 mmol). The resulting mixture was stirred overnight at reflux. Work-up: the mixture was concentrated and the residue was purified by flash column chromatography on silica gel with a 1:20 MeOH/CH2Cl2, to give 0.20 g (40%) of the product as white solid. MS m/z: 238 (M+H+).
The title compound was prepared as described in Example 158, except that 4,8-dichloro-1H-imidazo[4,5-c]quinoline was substituted for 4,8-dichloro-1-methyl-1H-imidazo[4,5-c]quinoline, and N-methylpiperazine for piperazine in step 9 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.33 (s, 1H), 8.17 (d, J=1.8 Hz, 1H), 7.61 (d, J=8.7 Hz, 1H), 7.42 (dd, J=9.0, 2.7 Hz, 1H), 4.24 (br, 4H), 2.49 (m, 4H), 2.22 (s, 3H). MS m/z: 302 (M+H+).
The title compound was prepared as described in Example 160, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.18 (s, 1H), 8.03 (d, J=2.1 Hz, 1H), 7.70 (d, J=9.0 Hz, 1H), 7.42 (dd, J=9.0, 2.4 Hz, 1H), 4.15 (t, J=5.0 Hz, 4H), 3.03 (t, J=5.1 Hz, 4H). MS m/z: 288 (M+H+).
The title compound was prepared as described in Example 160, except that triethyl orthoacetate was substituted for triethyl orthoformate in step 3 of that route. 1H NMR (300 MHz, CD3OD) δ: 7.97 (d, J=2.4 Hz, 1H), 7.74 (d, J=9.0 Hz, 1H), 7.45 (dd, J=9.0, 2.4 Hz, 1H), 4.88 (m, 4H), 3.39 (m, 4H), 2.92 (s, 3H), 2.64 (s, 3H). MS m/z: 316 (M+H+).
The title compound was prepared as described in Example 162, except that piperazine was substituted for N-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, D2O) δ: 7.49 (d, J=9.0 Hz, 1H), 7.24 (dd, J=9.0, 2.1 Hz, 1H), 7.19 (d, J=2.1 Hz, 1H), 4.42 (t, J=5.1 Hz, 4H), 3.45 (t, J=5.1 Hz, 4H), 2.45 (s, 3H). MS m/z: 302 (M+H+).
A 500 mL round bottom flask was charged with 5-chloro-2-nitroaniline (17.25 g, 0.1 mol) and 6 N HCl (100 mL). To the above was added dropwise a solution of NaNO2 (7.7 g, 0.105 mol) in water (30 mL) at 0-5° C. and the resulting mixture was stirred for 1 h. The diazotized solution was filtered and added slowly with stirring to an ice cold solution of SnCl2 (56.4 g, 0.25 mol) in concentrated HCl (70 mL). The reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:4, Rf=0.3). Work up: the yellow precipitate was collected by filtration, then partitioned between EtOAc (300 mL) and saturated aqueous NaOAc solution (200 mL). The organic layer was separated, dried over anhydrous MgSO4, and concentrated in vacuo, to give 8.4 g (45%) of the product. 1H NMR (300 MHz, CDCl3) δ: 8.94 (s, 1H), 8.06 (d, J=10.8 Hz, 1H), 7.70 (d, J=2.4 Hz, 1H), 6.66-6.62 (m, 1H), 3.81 (s, 2H).
A 250 mL round bottom flask was charged with 5-chloro-2-nitrophenylhydrazine (8.06 g, 0.043 mol), ethyl acetimidate hydrochloride (5.3 g, 0.043 mol) and pyridine (120 mL). The resulting mixture was stirred at room temperature overnight. The reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1, Rf=0.4). Work up: the solvent was evaporated under reduced pressure. The residue was partitioned between EtOAc (200 mL) and saturated aqueous Na2CO3 solution (200 mL). The organic layer was separated, dried over anhydrous MgSO4, and concentrated in vacuo, to give 6.4 g (65%) of the product. 1H NMR (300 MHz, CDCl3) δ: 9.56 (s, 1H), 8.07 (d, J=9.0 Hz, 1H), 7.54 (d, J=2.4 Hz, 1H), 6.66 (dd, J=9.0, 2.1 Hz, 1H), 4.73 (s, 2H), 2.10 (s, 3H). MS m/z: 229 (M+H+).
A 500 mL round bottom flask was charged with (1Z)-2-amino-1-azaprop-1-enyl)(5-chloro-2-nitrophenyl)amine (6.4 g, 28 mmol) and ethyl ether (25 mL). To the above was added dropwise a solution of ethyl 2-(chlorocarbonyl)acetate (7.65 g, 56 mmol) in ethyl ether (20 mL) at room temperature. The resulting mixture turned yellow from red. The reaction mixture was stirred at room temperature for 1 h, then mixed with anhydrous toluene (200 mL) and heated at reflux for 1 h. Work up: the reaction mixture was filtered. The filtrate was concentrated in vacuo, to give 4.2 g of the product, which was used directly in the next step without further purification.
A 50 mL round bottom flask was charged with ethyl (N-{(1Z)-2-[(5-chloro-2-nitrophenyl)amino]-1-methyl-2-azavinyl}carbamoyl)formate (4.2 g). It was heated at 180° C. for 1 h under N2. The reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1, Rf=0.3). Work up: the cooled mass was dissolved in CH2Cl2 (100 mL), washed with 0.5 N KOH solution (20 mL) and brine (30 mL) subsequently. The organic layer was dried over anhydrous MgSO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with a 1:6 EtOAc/Petroleum ether, to give 1.8 g of the product. 1H NMR (300 MHz, CDCl3) δ: 8.20 (d, J=8.7 Hz, 1H), 7.66 (dd, J=9.3, 2.4 Hz, 1H), 7.60 (d, J=2.1 Hz, 1H), 4.38-4.31 (m, 2H), 2.53 (s, 3H), 1.37-1.25 (m, 3H).
A 100 mL round bottom flask was charged with ethyl 1-(5-chloro-2-nitrophenyl)-3-methyl-1,2,4-triazole-5-carboxylate (1.8 g, 5.8 mmol), iron powder (5.87 g, 87 mmol) and HOAc (40 mL). The resulting mixture was heated at 90° C. for 1 h. Work up: the reaction mixture was filtered. The filtrate was concentrated in vacuo and mixed with 6 N HCl (50 mL). The precipitate formed was collected by filtration and dried, to give 0.8 g of the product which was used directly in the next step without further purification. MS m/z: 233 (M−H+).
The title compound was prepared as described in Example 92, except that 8-chloro-2-methyl-[1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one was substituted for 9-chloro-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one in step 3 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.39 (d, J=2.1 Hz, 1H), 8.04 (d, J=8.7 Hz, 1H), 7.65 (dd, J=9.0, 2.4 Hz, 1H), 2.75 (s, 3H).
The title compound was prepared as described in Example 92, except that 4,8-dichloro-2-methyl-[1,2,4]triazolo[1,5-a]quinoxaline was substituted for 5,9-dichloro-[1,2,4]triazolo[1,5-c]quinazoline in step 1 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.16-8.15 (m, 1H), 7.62-7.59 (m, 1H), 7.41-7.37 (m, 1H), 4.33-4.30 (m, 4H), 3.07-3.04 (m, 4H), 2.64 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared as described in Example 164, except that N-methylpiperazine was substituted for piperazine in step 7 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.17 (d, J=2.4 Hz, 1H), 7.62 (d, J=9.0 Hz, 1H), 7.40 (dd, J=8.7, 2.4 Hz, 1H), 4.38-4.35 (m, 4H), 2.64 (s, 3H), 2.61-2.58 (m, 4H), 2.37 (s, 3H). MS m/z: 317 (M+H+).
A 250 mL round bottom flask was charged with glycine ethyl ester hydrochloride (40 g, 0.29 mol), concentrated HCl (24 mL, 0.29 mol) and water (55 mL). To the above was added dropwise a solution of sodium nitrite (20 g, 0.29 mol) in water (30 mL) at −5° C. A second equivalent of hydrochloric acid and sodium nitrite were then added in the same manner. The resulting mixture was stirred at −5° C. for 20 min then extracted with ethyl ether (250 mL). The extract was dried over anhydrous MgSO4 and concentrated in vacuo. The yellowish oil residue was crystallized from hexane to afford 17 g (39%) of the product as white crystals. 1H NMR (300 MHz, CDCl3) δ: 9.92 (br, 1H), 4.39 (q, J=7.1 Hz, 2H), 1.38 (t, J=7.1 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 158.5, 132.9, 63.8, 13.9.
A 500 mL round bottom flask was charged with potassium t-butoxide (17.8 g, 0.16 mol) and dry DMF (200 mL). To the above was added dropwise a solution of 1-chloro-4-nitrobenzene (10 g, 0.063 mol) and ethyl chloroacetate (7.1 mL, 0.067 mol) in dry DMF (50 mL) at −5° C. The resulting dark-blue mixture was stirred at −5° C. for further 20 min then poured into 1 M HCl (500 mL) and extracted with ethyl ether (100 mL×5). The combined organic layers were washed with saturated aqueous NaHCO3 (250 mL) and brine (250 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 2-4% ethyl ether in petroleum ether, to afford 11.8 g (76%) of the product as orange oil. 1H NMR (300 MHz, CDCl3) δ: 8.06 (d, J=8.8 Hz, 1H), 7.42 (dd, J=8.8, 2.3 Hz, 1H), 7.34 (d, J=2.3 Hz, 1H), 4.16 (q, J=7.1 Hz, 2H), 3.98 (s, 2H), 1.24 (t, J=7.1 Hz, 3H). MS m/z: 242 (M−H+).
A 250 mL 3-necked round bottom flask was charged with ethyl 2-(5-chloro-2-nitrophenyl)acetate (2.0 g, 8.2 mmol) and dry ethyl ether (50 mL). To the above was added dropwise a solution of 1.5 M diisobutylaluminum hydride in toluene (11 ml, 16.5 mmol) at −78° C. The resulting mixture was stirred at −78° C. for further 1 h then quenched by slow addition of methanol (10 mL). The mixture was poured into 1 M HCl (200 mL) and extracted with ethyl ether (100 mL×2). The combined organic layers were washed with saturated aqueous NaHCO3 (100 mL) and brine (100 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 4-20% ethyl ether in petroleum ether, to afford 1.1 g (70%) of the product as orange oil. 1H NMR (300 MHz, CDCl3) δ: 9.83 (t, J=0.7 Hz, 1H), 8.12 (d, J=8.8 Hz, 1H), 7.46 (dd, J=8.8, 2.3 Hz, 1H), 7.31 (d, J=2.3 Hz, 1H), 4.13 (s, 2H). MS m/z: 198 (M−H+).
A 1 L round bottom flask was charged with 2-(5-chloro-2-nitrophenyl)acetaldehyde (8.5 g, 43 mmol), pyrrolidine (4.3 mL, 51 mmol), crushed 4A molecular sieves (18 g) and dry toluene (50 mL). The reaction mixture was stirred for 2 h at room temperature under N2 and developed a dark-red color.
To the above dark-red mixture were added Et3N (12 mL, 86 mmol) and THF (150 mL), followed by a very slow addition in the dark of a solution of ethyl chlorooximidoacetate (13 g, 86 mmol) in THF (250 mL). The resulting mixture was stirred in the dark overnight at room temperature, and then filtered and concentrated in vacuo.
The residue was added to EtOH (150 mL) and concentrated HCl (36 mL, 0.43 mol). The resulting mixture was stirred at 50° C. overnight then concentrated in vacuo. It was poured into saturated aqueous NaHCO3 (300 mL) and extracted with CHCl3 (100 mL×5). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 40-100% CH2Cl2 in petroleum ether, to afford 8.8 g (70%) of the product as dark-red oil. 1H NMR (300 MHz, CDCl3) δ: 8.59 (s, 1H), 8.18 (d, J=8.8 Hz, 1H), 7.57 (dd, J=8.8, 2.2 Hz, 1H), 7.39 (d, J=2.2 Hz, 1H), 4.31 (q, J=7.1 Hz, 2H), 1.29 (t, J=7.1 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ: 159.3, 157.3, 152.9, 146.6, 139.7, 132.6, 129.9, 126.6, 125.2, 118.1, 62.5, 13.8.
A 250 mL round bottom flask was charged with ethyl 4-(5-chloro-2-nitrophenyl)isoxazole-3-carboxylate (3.4 g, 11 mmol), Na2S2O4 (85% purity, 4.7 g, 23 mmol), EtOH (120 mL) and H2O (50 mL). The resulting mixture was stirred at reflux overnight and then concentrated in vacuo. The residue was mixed with saturated aqueous NaHCO3 (200 mL) and extracted with CHCl3 (100 mL×5). The combined organic layers were dried over anhydrous Na2SO4 then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 5-20% MeOH in CH2Cl2, to afford 1.2 g (47%) of the product as white solid. 1H NMR (300 MHz, DMSO-d6) δ: 11.83 (br, 1H), 10.05 (s, 1H), 8.14 (s, 1H), 7.48 (d, J=8.7 Hz, 1H), 7.31 (d, J=8.7 Hz, 1H).
A 100 mL round bottom flask was charged with 8-chloroisoxazolo[3,4-c]quinolin-4(5H)-one (1.2 g, 5.5 mmol) and POCl3 (50 mL). After N,N-diisopropylethylamine (0.95 mL, 5.5 mmol) was added dropwise at 0° C., the resulting mixture was refluxed overnight (16 h) and then concentrated under reduced pressure. The residue was carefully diluted with saturated aqueous NaHCO3 (150 mL), then extracted with CH2Cl2 (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 then concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with CH2Cl2 (containing 1% Et3N), to afford 0.50 g (38%) of the product as light-yellow solid. 1H NMR (300 MHz, CDCl3) δ: 9.47 (s, 1H), 7.99 (d, J=2.4 Hz, 1H), 7.96 (d, J=8.9 Hz, 1H), 7.62 (dd, J=8.9, 2.4 Hz, 1H).
A 20 mL microwave reaction tube was charged with 4,8-dichloroisoxazolo[3,4-c]quinoline (200 mg, 0.84 mmol), N-methylpiperazine (0.28 mL, 2.5 mmol) and THF (10 mL). The tube was sealed and heated at 90° C. for 1 h in a Biotage microwave reactor. Work-up: the reaction mixture was poured into saturated aqueous NaHCO3 (100 mL) and extracted with CH2Cl2 (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with CH2Cl2 (saturated with NH3), to afford 150 mg (59%) of the product as tan solid. 1H NMR (300 MHz, CD3OD) δ: 9.73 (s, 1H), 7.91 (d, J=2.4 Hz, 1H), 7.47 (d, J=8.8 Hz, 1H), 7.35 (dd, J=8.8, 2.4 Hz, 1H), 4.23 (m, 4H), 2.62 (m, 4H), 2.36 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared as described in Example 166, except that piperazine was substituted for N-methylpiperazine in step 9 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.72 (s, 1H), 7.90 (d, J=2.4 Hz, 1H), 7.46 (d, J=8.8 Hz, 1H), 7.35 (dd, J=8.8, 2.4 Hz, 1H), 4.18 (m, 4H), 2.97 (m, 4H). MS m/z: 289 (M+H+).
The title compound was prepared as described in Example 39, except that piperazine was substituted for N-methylpiperazine in step 3 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.70 (s, 1H), 8.22 (s, 1H), 7.62 (s, 1H), 4.41-4.38 (m, 4H), 3.08 (t, J=5.4 Hz, 4H). MS m/z: 323 (M+H+).
The title compound was prepared as described in Example 236, except that piperazine was substituted for N-methylpiperazine in step 8 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.40 (d, J=2.4 Hz, 1H), 7.61 (t, J=8.4 Hz, 1H), 7.47 (d, J=8.4 Hz, 1H), 4.55 (br, 4H), 3.08 (t, J=5.4 Hz, 4H). MS m/z: 341 (M+H+).
The title compound was prepared as described in Example 21, except that 2,3-dichloro-5-fluoro-6-(trifluoromethyl)quinoxaline (prepared as described in Example 132, step 7) was substituted for 2,3-dichloro-6-methylquinoxaline as the starting material. 1H NMR (300 MHz, DMSO-d6) δ: 10.08 (s, 1H), 8.17 (d, J=8.7 Hz, 1H), 7.64 (t, J=6.9 Hz, 1H), 4.34 (br, 4H), 2.52 (m, 4H), 2.23 (s, 3H). MS m/z: 355 (M+H+).
The title compound was prepared as described in Example 27, except that 2,3-dichloro-5-fluoro-6-(trifluoromethyl)quinoxaline (prepared as described in Example 132, step 7) was substituted for 2,3-dichloro-6-(trifluoromethyl)quinoxaline as the starting material. 1H NMR (300 MHz, DMSO-d6) δ: 7.89 (t, J=8.7 Hz, 1H), 7.62 (d, J=8.7 Hz, 1H), 4.46 (br, 4H), 2.53 (t, J=5.4 Hz, 4H), 2.24 (s, 3H). MS m/z: 356 (M+H+).
The title compound was prepared as described in Example 171, except that piperazine was substituted for N-methylpiperazine in step 1 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 7.77 (t, J=8.4 Hz, 1H), 7.53 (d, J=9.0 Hz, 1H), 4.56 (m, 4H), 3.44 (m, 4H). MS m/z: 342 (M+H+).
The title compound was prepared as described in Examples 88 and 90, except that 2-(tributylstannyl)propene was substituted for tri-n-butyl(vinyl)tin as the coupling reactant. 1H NMR (300 MHz, CDCl3) δ: 9.17 (s, 1H), 7.62 (d, J=8.4 Hz, 1H), 7.53 (s, 1H), 7.37 (d, J=8.7 Hz, 1H), 4.44 (br, 4H), 3.06 (m, 1H), 2.61 (t, J=5.1 Hz, 4H), 2.37 (s, 3H), 1.33 (d, J=6.9 Hz, 6H). MS m/z: 310 (M+H+).
The title compound was prepared as described in Example 88, except that 1-propenyltributyltin was substituted for tri-n-butyl(vinyl)tin as the coupling reactant. 1H NMR (300 MHz, CDCl3) δ: 9.14 (s, 1H), 7.64-7.57 (m, 2H), 7.48 (m, 1H), 6.53-6.45 (m, 1H), 6.39-6.27 (m, 0.5H), 5.95-5.84 (m, 0.5H), 4.48 (br, 4H), 2.65 (t, J=4.8 Hz, 4H), 2.40 (s, 3H), 1.98-1.92 (m, 3H). MS m/z: 308 (M+H+).
The title compound was prepared as described in Example 90, except that (E)-4-(4-methylpiperazin-1-yl)-8-(prop-1-enyl)-[1,2,4]triazolo[4,3-a]quinoxaline (Example 174) was substituted for 4-(4-methylpiperazin-1-yl)-8-vinyl-[1,2,4]triazolo[4,3-a]quinoxaline (Example 88) as the starting material. 1H NMR (300 MHz, CDCl3) δ: 9.15 (s, 1H), 7.59 (d, J=8.4 Hz, 1H), 7.50 (s, 1H), 7.28 (d, J=8.1 Hz, 1H), 4.43 (br, 4H), 2.71 (t, J=7.6 Hz, 2H), 2.60 (t, J=4.8 Hz, 4H), 2.36 (s, 3H), 1.71 (m, 2H), 0.97 (t, J=7.4 Hz, 3H). MS m/z: 310 (M+H+).
A 50 mL round bottom flask was charged with 8-bromo-4-(4-methylpiperazin-1-yl)-[1,2,4]triazolo[4,3-a]quinoxaline (Example 54, 0.20 g, 0.6 mmol), isopropylamine (1 mL), L-proline (0.13 g, 1.13 mmol), CuI (0.11 g, 0.6 mmol), K3PO4 (0.11 g, 1.2 mmol) and DMSO (20 mL). The resulting mixture was heated at 90° C. overnight. Work-up: the reaction mixture was diluted with water (100 mL) and extracted with EtOAc (100 mL×2). The combined organic layers were dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 5% MeOH in CH2Cl2, to afford 80 mg (43%) of the product as yellow solid. 1H NMR (300 MHz, CDCl3) δ: 9.05 (s, 1H), 7.51 (d, J=9.0 Hz, 1H), 6.77 (s, 1H), 6.75 (d, J=8.4 Hz, 1H), 4.31 (t, J=4.8 Hz, 4H), 3.72 (m, 1H), 2.63 (t, J=5.1 Hz, 4H), 2.38 (s, 3H), 1.28 (d, J=6.0 Hz, 6H). MS m/z: 326 (M+H+).
The title compound was prepared as described in Example 54, except that 4-(piperazin-1-yl)-8-(trifluoromethyl)imidazo[1,2-a]quinoxaline hydrochloride (EXAMPLE 178) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, CDCl3) δ: 8.00 (d, J=1.5 Hz, 1H), 7.90 (s, 1H), 7.72 (d, J=8.7 Hz, 1H), 7.65-7.59 (m, 2H), 4.52 (br, 4H), 2.63 (t, J=4.8 Hz, 4H), 2.39 (s, 3H). MS m/z: 336 (M+H+).
The title compound was prepared as described as in Example 180, except that 4-(trifluoromethyl)benzene-1,2-diamine was substituted for 4-chloro-5-fluorobenzene-1,2-diamine as the starting material. 1H NMR (300 MHz, D2O) δ: 8.10 (d, J=1.5 Hz, 1H), 7.88 (s, 1H), 7.59 (d, J=1.5 Hz, 1H), 7.54-7.47 (m, 2H), 4.34 (t, J=5.1 Hz, 4H), 3.42 (t, J=5.1 Hz, 4H). MS m/z: 322 (M+H+).
The title compound was prepared as described in Example 54, except that 8-chloro-7-fluoro-4-(piperazin-1-yl)imidazo[1,2-a]quinoxaline HCl salt (Example 180) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, CDCl3) δ: 7.85 (d, J=1.5 Hz, 1H), 7.67 (d, J=6.9 Hz, 1H), 7.60 (d, J=1.5 Hz, 1H), 7.39 (d, J=10.2 Hz, 1H), 4.44 (t, J=4.5 Hz, 4H), 2.58 (t, J=5.1 Hz, 4H), 2.35 (s, 3H). MS m/z: 320 (M+H+).
A 50 mL round bottom flask was charged with tert-butyl 4-(3,6-dichloro-7-fluoroquinoxalin-2-yl)piperazinecarboxylate (prepared as described in Example 31, 1.5 g, 3.6 mmol) and 2,2-diethoxyethylamine (10 mL). The resulting mixture was stirred at reflux for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:5). Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in EtOAc (200 mL) and washed with brine (100 mL). The organic layer was dried over anhydrous Na2SO4 and then concentrated in vacuo to afford the title compound.
A 50 mL round bottom flask was charged with tert-butyl 4-{3-[(2,2-diethoxyethyl)amino]-6-chloro-7-fluoroquinoxalin-2-yl}piperazinecarboxylate from step 4, p-toluenesulfonic acid (1.37 g, 7.3 mmol) and isopropanol (25 mL). The resulting mixture was stirred at reflux for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:3). Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in EtOAc (200 mL) and washed with brine (100 mL). The organic layer was dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with a 1:3 EtOAc/Petroleum ether to afford the title compound.
The HCl salt of the title compound was prepared as described in Example 52 step 6, except that tert-butyl 4-(8-chloro-7-fluoro-10-hydroimidazo[1,2-a]quinoxalin-4-yl)piperazinecarboxylate was substituted for tert-butyl 4-(8-bromo-10-hydro-1,2,4-triazolo[4,3-a]quinoxalin-4-yl)piperazinecarboxylate. 1H NMR (300 MHz, CDCl3) δ: 7.83 (d, J=5.4 Hz, 1H), 7.66 (d, J=6.9 Hz, 1H), 7.59 (s, 1H), 7.38 (d, J=9.9 Hz, 1H), 4.34 (br, 4H), 3.02 (br, 4H). MS m/z: 306 (M+H+).
The title compound was prepared as described in Examples 37 and 179, except that 2,3-dichloro-6,7-difluoroquinoxaline was substituted for 2,3,7-trichloro-6-fluoroquinoxaline in step 3 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.61 (d, J=1.5 Hz, 1H), 8.38 (dd, J=11.1, 7.8 Hz, 1H), 7.68 (d, J=1.2 Hz, 1H), 7.56 (dd, J=12.0, 8.1 Hz, 1H), 4.31 (br, 4H), 2.49 (m, 4H), 2.23 (s, 3H). MS m/z: 304 (M+H+).
The title compound was prepared as described in Example 181, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 8.29 (d, J=1.5 Hz, 1H), 7.98 (dd, J=11.1, 7.8 Hz, 1H), 7.60 (d, J=1.5 Hz, 1H), 7.46 (dd, J=11.7, 8.1 Hz, 1H), 4.29 (t, J=5.1 Hz, 4H), 3.00 (t, J=5.1 Hz, 4H). MS m/z: 290 (M+H+).
The title compound was prepared as described as in Example 178. It was separated from the other regio-isomer by flash column chromatography. 1H NMR (300 MHz, DMSO-d6) δ: 9.60 (br, 2H), 8.83 (d, J=1.8 Hz, 1H), 8.41 (d, J=8.4 Hz, 1H), 7.92 (d, J=1.5 Hz, 1H), 7.77 (d, J=1.5 Hz, 1H), 7.70 (dd, J=8.4, 1.8 Hz, 1H), 4.62 (br, 4H), 3.28 (br, 4H). MS m/z: 322 (M+H+).
The HCl salt of the title compound was prepared as described in Example 34, except that 4-bromo-3-fluoroaniline was substituted for 4-fluoro-3-methylaniline as the starting material. 1H NMR (300 MHz, DMSO-d6) δ: 9.97 (s, 1H), 8.65 (d, J=6.6 Hz, 1H), 7.46 (d, J=10.5 Hz, 1H), 4.37 (br, 4H), 3.01 (t, J=5.1 Hz, 4H). MS m/z: 351 (M+H+).
The title compound was prepared as described in Example 54, except that 8-bromo-7-fluoro-4-(piperazin-1-yl)-[1,2,4]triazolo[4,3-a]quinoxaline HCl salt (Example 184) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, DMSO-d6) δ: 9.95 (s, 1H), 8.62 (d, J=6.6 Hz, 1H), 7.45 (d, J=10.2 Hz, 1H), 4.32 (br, 4H), 3.29 (m, 4H), 2.22 (s, 3H). MS m/z: 365 (M+H+).
The HCl salt of the title compound was prepared as described in Example 29, except that 5-fluoro-4-(trifluoromethyl)benzene-1,2-diamine (prepared according to Example 34) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material. 1H NMR (300 MHz, DMSO-d6) δ: 9.59 (br, 1H), 8.64 (d, J=7.2 Hz, 1H), 7.84 (d, J=11.7 Hz, 1H), 4.65-4.33 (m, 8H). MS m/z: 342 (M+H+).
The title compound was prepared as described in Example 54, except that 7-fluoro-4-(piperazin-1-yl)-8-(trifluoromethyl)tetrazolo[1,5-a]quinoxaline HCl salt was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt as the starting material. 1H NMR (300 MHz, CDCl3) δ: 8.62 (d, J=6.9 Hz, 1H), 7.50 (d, J=11.4 Hz, 1H), 4.80-4.22 (m, 4H), 2.63 (m, 4H), 2.40 (s, 3H). MS m/z: 356 (M+H+).
The HCl salt of the title compound was prepared as described in Examples 29 and 180, except that 4-chloro-5-fluorobenzene-1,2-diamine was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material. 1H NMR (300 MHz, DMSO-d6) δ: 8.48 (d, J=7.2 Hz, 1H), 7.67 (d, J=10.8 Hz, 1H), 4.23 (br, 4H), 2.86 (m, 4H). MS m/z: 307 (M+H+).
The title compound was prepared as described in Example 54, except that 8-chloro-7-fluoro-4-(piperazin-1-yl)tetrazolo[1,5-a]quinoxaline HCl salt (Example 188) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, DMSO-d6) δ: 8.52 (d, J=7.5 Hz, 1H), 7.72 (d, J=10.2 Hz, 1H), 4.30 (br, 4H), 2.57 (br, 4H), 2.28 (s, 3H). MS m/z: 321 (M+H+).
The title compound was prepared as described in Examples 37 and 27, except that 2,3-dichloro-6,7-difluoroquinoxaline was substituted for 2,3-dichloro-6-(trifluoromethyl)quinoxaline as the starting material of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.02 (dd, J=10.2, 7.8 Hz, 1H), 7.78 (dd, J=11.4, 7.8 Hz, 1H), 4.26 (br, 4H), 2.50 (m, 4H), 2.24 (s, 3H). MS m/z: 306 (M+H+).
The HCl salt of the title compound was prepared as described in Examples 37 and 29, except that 2,3-dichloro-6,7-difluoroquinoxaline was substituted for 2,3-dichloro-6-(trifluoromethyl)quinoxaline as the starting material of that route. 1H NMR (300 MHz, DMSO-d6) δ: 9.65 (br, 3H), 8.55 (dd, J=10.2, 7.8 Hz, 1H), 7.87 (dd, J=11.7, 7.8 Hz, 1H), 4.50 (br, 4H), 3.30 (m, 4H). MS m/z: 292 (M+H+).
The HCl salt of the title compound was prepared as described in Examples 23 and 196, except that 5-chloro-3-fluorobenzene-1,2-diamine was substituted for 4-(trifluoromethyl)benzene-1,2-diamine. 1H NMR (300 MHz, DMSO-d6) δ: 9.59 (s, 1H), 7.46-7.39 (m, 2H), 4.29 (br, 4H), 2.87 (br, 4H). MS m/z: 307 (M+H+).
The title compound was prepared as described in Example 54, except that 7-bromo-4-(piperazin-1-yl)-[1,2,4]triazolo[4,3-a]quinoxaline HCl salt (Example 53) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, CDCl3) δ: 9.12 (s, 1H), 7.83 (d, J=2.1 Hz, 1H), 7.57 (d, J=8.7 Hz, 1H), 7.38 (dd, J=8.7, 2.1 Hz, 1H), 4.48 (br, 4H), 2.60 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 347 (M+H+).
The title compound was prepared as described in Examples 29 and 52, except that 4-bromobenzene-1,2-diamine was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material. 1H NMR (300 MHz, DMSO-d6) δ: 9.58 (s, 2H), 8.30 (d, J=9.0 Hz, 1H), 7.96 (s, 1H), 7.70 (d, J=9.0 Hz, 1H), 4.52 (br, 4H), 3.29 (br, 4H). MS m/z: 334 (M+H+).
The title compound was prepared as described in Example 54, except that 7-bromo-4-(piperazin-1-yl)tetrazolo[1,5-a]quinoxaline hydrochloride (Example 194) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, CDCl3) δ: 8.21 (d, J=8.4 Hz, 1H), 7.92 (s, 1H), 7.51 (d, J=8.7 Hz, 1H), 4.44 (br, 4H), 2.61 (t, J=4.8 Hz, 4H), 2.37 (s, 3H). MS m/z: 348 (M+H+).
The title compound was prepared as described in Example 122 step 1, except that 4-chloro-2-fluoroaniline was substituted for 3-chloro-4-(trifluoromethyl)aniline.
The title compound was prepared as described in Example 236 step 5, except that 4-chloro-2-fluoro-6-iodoaniline was substituted for 6-bromo-2-fluoro-3-(trifluoromethyl)aniline.
The HCl salt of the title compound was prepared as described in Example 21, except that 5-chloro-3-fluorobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material. 1H NMR (300 MHz, DMSO-d6) δ: 9.99 (s, 1H), 8.23 (s, 1H), 7.49 (d, J=10.8 Hz, 1H), 4.26 (br, 4H), 2.85 (br, 4H). MS m/z: 307 (M+H+).
The title compound was prepared as described in Example 54, except that 8-chloro-6-fluoro-4-(piperazin-1-yl)-[1,2,4]triazolo[4,3-a]quinoxaline HCl salt (Example 196) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, DMSO-d6) δ: 9.99 (s, 1H), 8.24 (s, 1H), 7.53 (d, J=10.5 Hz, 1H), 4.33 (br, 4H), 3.30 (br, 4H), 2.23 (s, 3H). MS m/z: 321 (M+H+).
The HCl salt of the title compound was prepared as described in Examples 21 and 184, except that 4-bromo-5-fluorobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine. 1H NMR (300 MHz, DMSO-d6) δ: 9.86 (s, 1H), 8.27 (d, J=9.3 Hz, 1H), 7.73 (d, J=6.6 Hz, 1H), 4.21 (br, 4H), 2.80 (br, 4H). MS m/z: 351 (M+H+).
The title compound was prepared as described in Example 54, except that 7-bromo-8-fluoro-4-(piperazin-1-yl)-[1,2,4]triazolo[4,3-a]quinoxaline HCl salt (Example 198) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, DMSO-d6) δ: 9.90 (s, 1H), 8.31 (d, J=9.6 Hz, 1H), 7.79 (d, J=6.6 Hz, 1H), 4.27 (br, 4H), 2.46 (br, 4H), 2.22 (s, 3H). MS m/z: 365 (M+H+).
The HCl salt of the title compound was prepared as described in Examples 18 and 186, except that 5-fluoro-4-(trifluoromethyl)benzene-1,2-diamine (prepared according to Example 34) was substituted for 4-methylbenzene-1,2-diamine as the starting material. 1H NMR (300 MHz, CDCl3) δ: 8.19 (d, J=9.3 Hz, 1H), 8.04 (d, J=6.6 Hz, 1H), 4.41 (br, 4H), 3.09 (m, 4H). MS m/z: 342 (M+H+).
The title compound was prepared as described in Example 54, except that 8-fluoro-4-(piperazin-1-yl)-7-(trifluoromethyl)tetrazolo[1,5-a]quinoxaline HCl salt was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt as the starting material. 1H NMR (300 MHz, CDCl3) δ: 8.19 (d, J=9.3 Hz, 1H), 8.04 (d, J=6.3 Hz, 1H), 4.44 (br, 4H), 2.62 (m, 4H), 2.38 (s, 3H). MS m/z: 356 (M+H+).
The title compound was prepared as described in Example 18, except that 4-chloro-5-fluorobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CDCl3) δ: 8.14 (d, J=8.1 Hz, 1H), 7.83 (d, J=7.2 Hz, 1H), 4.38 (br, 4H), 3.08 (t, J=5.1 Hz, 4H). MS m/z: 308 (M+H+).
The title compound was prepared as described in Example 54, except that 7-chloro-8-fluoro-4-(piperazin-1-yl)tetrazolo[1,5-a]quinoxaline (Example 202) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, CDCl3) δ: 8.14 (d, J=7.8 Hz, 1H), 7.83 (d, J=6.9 Hz, 1H), 4.42 (br, 4H), 2.61 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 322 (M+H+).
The title compound was prepared as described in Example 18, except that 4-bromobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material and N-methylpiperazine for piperazine in step 4 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.52 (d, J=2.1 Hz, 1H), 7.68 (dd, J=8.7, 2.1 Hz, 1H), 7.60 (d, J=8.7 Hz, 1H), 4.43 (br, 4H), 2.62 (t, J=5.3 Hz, 4H), 2.38 (s, 3H). MS m/z: 348 (M+H+).
The title compound was prepared as described in Example 18, except that 4-bromobenzene-1,2-diamine was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CDCl3) δ: 8.50 (d, J=2.1 Hz, 1H), 7.67 (dd, J=8.7, 2.1 Hz, 1H), 7.59 (d, J=8.7 Hz, 1H), 4.38 (br, 4H), 3.08 (m, 4H). MS m/z: 334 (M+H+).
The title compound was prepared as described in Example 29, except that 3-fluoro-5-(trifluoromethyl)benzene-1,2-diamine (prepared as described in Example 48 steps 1-4) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, DMSO-d6) δ: 9.58 (br, 2H), 8.48 (s, 1H), 8.07 (dd, J=10.8, 1.8 Hz, 1H), 4.61 (br, 4H), 3.33 (t, J=5.1 Hz, 4H). MS m/z: 342 (M+H+).
The title compound was prepared as described in Example 54, except that 6-fluoro-4-(piperazin-1-yl)-8-(trifluoromethyl)tetrazolo[1,5-a]quinoxaline hydrochloride (Example 206) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, DMSO-d6) δ: 8.38 (s, 1H), 7.97 (dd, J=10.8, 2.1 Hz, 1H), 4.37 (br, 4H), 2.54 (t, J=5.1 Hz, 4H), 2.25 (s, 3H). MS m/z: 356 (M+H+).
The title compound was prepared as described in Example 196, except that 4-bromo-2-fluoroaniline was substituted for 4-chloro-2-fluoroaniline in step 1, and N-methylpiperazine for N-BOC piperazine in step 7 of that route. 1H NMR (300 MHz, CD3OD) δ: 9.75 (s, 1H), 8.14 (d, J=1.5 Hz, 1H), 7.44 (dd, J=9.6, 1.8 Hz, 1H), 4.45 (br, 4H), 2.64 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 365 (M+H+).
The title compound was prepared as described in Example 208, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 9.75 (s, 1H), 8.13 (d, J=1.5 Hz, 1H), 7.44 (dd, J=9.6, 1.8 Hz, 1H), 4.41 (br, 4H), 3.01 (t, J=5.1 Hz, 4H). MS m/z: 351 (M+H+).
The title compound was prepared as described in Example 18, except that 5-bromo-3-fluorobenzene-1,2-diamine (prepared as described in Example 208, steps 1-2) was substituted for 4-methylbenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 8.34 (t, J=1.8 Hz, 1H), 7.50 (dd, J=9.9, 1.8 Hz, 1H), 4.47 (br, 4H), 2.63 (t, J=5.1 Hz, 4H), 2.39 (s, 3H). MS m/z: 366 (M+H+).
The HCl salt of the title compound was prepared as described in Example 29, except that 4-bromo-5-fluorobenzene-1,2-diamine (prepared as described in Example 184 steps 1-4) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, DMSO-d6) δ: 9.45 (br, 2H), 8.70 (d, J=6.6 Hz, 1H), 7.75 (d, J=9.9 Hz, 1H), 4.52 (br, 4H), 3.30 (t, J=5.7 Hz, 4H). MS m/z: 352 (M+H+).
The title compound was prepared as described in Example 54, except that 8-bromo-7-fluoro-4-(piperazin-1-yl)tetrazolo[1,5-a]quinoxaline HCl salt (Example 211) was substituted for 8-bromo-4-piperazinyl-10-hydro-1,2,4-triazolo[4,3-a]quinoxaline HCl salt (Example 52). 1H NMR (300 MHz, CDCl3) δ: 8.57 (d, J=6.9 Hz, 1H), 7.46 (d, J=9.3 Hz, 1H), 4.46 (br, 4H), 2.61 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 366 (M+H+).
A 25 mL round bottom flask was charged with 2,6-dichloro-3-hydrazinylquinoxaline (prepared as described in Example 1, steps 1-3, 0.1 g, 0.44 mmol) and 1N aqueous HCl solution (2 mL). To the suspension was added dropwise a solution of sodium nitrite (45 mg, 0.44 mmol) in water (0.5 mL) at 0° C. The resulting mixture was stirred at 0-5° C. for further 0.5 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1). Work-up: the precipitate was collected by filtration and washed with water to afford 100 mg (95%) of the product as light yellow solids. 1H NMR (300 MHz, DMSO-d6) δ: 8.70 (d, J=2.1 Hz, 1H), 8.27 (d, J=8.7 Hz, 1H), 8.00 (dd, J=8.7, 2.1 Hz, 1H).
The title compound was prepared as described in Example 19, except that octahydropyrrolo[1,2-a]pyrazine was substituted for piperazine in that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.33 (d, J=2.1 Hz, 1H), 7.72 (d, J=8.7 Hz, 1H), 7.66 (dd, J=8.7, 2.1 Hz, 1H), 5.44-5.37 (m, 2H), 3.33-3.16 (m, 2H), 3.08-2.92 (m, 2H), 2.29-2.21 (m, 1H), 2.14-2.05 (m, 2H), 1.90-1.66 (m, 3H), 1.50-1.41 (m, 1H). MS m/z: 330 (M+H+).
The title compound was prepared as described in Example 141, except that 2-amino-5-(trifluoromethyl)benzoic acid was substituted for 2-amino-5-chlorobenzoic acid as the starting material, and ethyl orthoacetate was substituted for ethyl orthoformate in step 4 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.21 (s, 1H), 7.79 (m, 2H), 4.21 (br, 4H), 2.73 (s, 3H), 2.49 (m, 4H), 2.24 (s, 3H). MS m/z: 351 (M+H+).
The title compound was prepared as described in Example 214, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.19 (s, 1H), 7.77 (m, 2H), 4.15 (m, 4H), 2.85 (m, 4H), 2.72 (s, 3H). MS m/z: 337 (M+H+).
A 500 mL 3-necked round bottom flask was charged with 2-amino-4-fluorobenzoic acid (5.0 g, 32.3 mmol) and anhydrous DMF (75 mL). To the above was added N-chlorosuccinimide (4.3 g, 32.3 mmol) in several portions at room temperature. The resulting mixture was heated at 50° C. for 2.5 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1, Rf=0.4). Work-up: the mixture was poured into water and filtered. The solid collected was washed with water and dried, to afford 4.53 g (74%) of the product, which was used in the next step without further purification.
The title compound was prepared as described in Example 141, except that 2-amino-5-chloro-4-fluorobenzoic acid was substituted for 2-amino-5-chlorobenzoic acid in step 1, and ethyl orthoacetate was substituted for ethyl orthoformate in step 4 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.07 (d, J=7.8 Hz, 1H), 7.55 (d, J=11.4 Hz, 1H), 4.15 (t, J=4.8 Hz, 4H), 2.70 (s, 3H), 2.46 (t, J=4.8 Hz, 4H), 2.23 (s, 3H). MS m/z: 335 (M+H+).
The title compound was prepared as described in Example 216, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.02 (d, J=8.4 Hz, 1H), 7.50 (d, J=11.7 Hz, 1H), 4.08 (t, J=4.8 Hz, 4H), 2.83 (t, J=4.5 Hz, 4H), 2.69 (s, 3H). MS m/z: 321 (M+H+).
The title compound was prepared as described in Example 166, except that 4-nitrobenzotrifluoride was substituted for 1-chloro-4-nitrobenzene as the starting material. 1H NMR (300 MHz, CDCl3) δ: 9.33 (s, 1H), 8.02 (s, 1H), 7.66 (s, 2H), 4.35 (t, J=3.3 Hz, 4H), 2.61 (t, J=4.5 Hz, 4H), 2.38 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Example 218, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CDCl3) δ: 9.33 (s, 1H), 8.02 (s, 1H), 7.66 (s, 2H), 4.33 (t, J=3.3 Hz, 4H), 3.09 (t, J=4.2 Hz, 4H). MS m/z: 323 (M+H+).
The title compound was prepared as described in Example 166, except that 3-nitrobenzotrifluoride was substituted for 1-chloro-4-nitrobenzene as the starting material. 1H NMR (300 MHz, CDCl3) δ: 9.32 (s, 1H), 7.85 (m, 2H), 7.42 (dd, J=8.1, 1.2 Hz, 1H), 4.32 (m, 4H), 2.60 (m, 4H), 2.37 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Example 220, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CDCl3) δ: 9.33 (s, 1H), 7.86 (m, 2H), 7.42 (dd, J=7.8, 1.5 Hz, 1H), 4.27 (m, 4H), 3.06 (m, 4H). MS m/z: 323 (M+H+).
The title compound was prepared as described in Example 166, except that 1-bromo-4-nitrobenzene was substituted for 1-chloro-4-nitrobenzene as the starting material. 1H NMR (300 MHz, CDCl3) δ: 9.24 (s, 1H), 7.79 (d, J=1.8 Hz, 1H), 7.48 (m, 2H), 4.28 (t, J=4.8 Hz, 4H), 2.59 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 347 (M+H+).
The title compound was prepared as described in Example 222, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CDCl3) δ: 9.24 (s, 1H), 7.89 (d, J=2.1, 1H), 7.48 (m, 2H), 4.24 (t, J=4.8 Hz, 4H), 3.06 (t, J=5.1 Hz, 4H). MS m/z: 333 (M+H+).
A 250 mL round bottom flask was charged with 4-chloro-2-nitrotoluene (10.0 g, 58.3 mmol), N,N-dimethylformamide dimethyl acetal (23 mL) and DMF (100 mL). The resulting mixture was stirred at reflux overnight. Work-up: the reaction mixture was concentrated in vacuo. The residue was used as such for the next step. 1H NMR (300 MHz, CDCl3) δ: 7.85 (d, J=2.1 Hz, 1H), 7.38 (d, J=8.7 Hz, 1H), 7.26 (m, 1H), 6.93 (d, J=16.2 Hz, 1H), 5.83 (d, J=13.5 Hz, 1H), 2.91 (s, 6H).
The title compound was prepared as described in Example 166, except that (E)-2-(4-chloro-2-nitrophenyl)-N,N-dimethylethenamine was substituted for [(1E)-2-(5-chloro-2-nitrophenyl)vinyl]pyrrolidine in step 4 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.23 (s, 1H), 7.68 (d, J=8.4 Hz, 1H), 7.61 (d, J=1.8 Hz, 1H), 7.18 (dd, J=8.4, 2.1 Hz, 1H), 4.23 (t, J=4.8 Hz, 1H), 2.58 (t, J=5.1 Hz, 1H), 2.36 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared as described in Example 224, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, DMSO-d6) δ: 10.15 (s, 1H), 7.99 (d, J=8.4 Hz, 1H), 7.46 (d, J=2.1 Hz, 1H), 7.26 (dd, J=8.1, 2.1 Hz, 1H), 4.09 (t, J=4.5 Hz, 1H), 2.83 (t, J=5.1 Hz, 1H). MS m/z: 289 (M+H+).
The title compound was prepared as described in Example 224, except that 4,5-difluoro-2-nitrotoluene was substituted for 4-chloro-2-nitrotoluene as the starting material. 1H NMR (300 MHz, CDCl3) δ: 9.19 (s, 1H), 7.51 (dd, J=10.0, 8.2 Hz, 1H), 7.37 (dd, J=12.0, 7.8 Hz, 1H), 4.26 (t, J=5.1 Hz, 4H), 2.59 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 305 (M+H+).
The title compound was prepared as described in Example 226, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, D2O) δ: 9.70 (s, 1H), 7.76 (m, 1H), 7.53 (m, 1H), 4.55 (br, 4H), 3.55 (t, J=5.1 Hz, 4H). MS m/z: 291 (M+H+).
The title compound was prepared as described in Example 224, except that 4-bromo-2-nitrotoluene was substituted for 4-chloro-2-nitrotoluene as the starting material. 1H NMR (300 MHz, CDCl3) δ: 9.24 (s, 1H), 7.78 (d, J=1.8 Hz, 1H), 7.61 (d, J=8.1 Hz, 1H), 7.31 (dd, J=8.1, 1.8 Hz, 1H), 4.29 (t, J=4.8 Hz, 4H), 2.58 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 347 (M+H+).
The title compound was prepared as described in Example 228, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CDCl3) δ: 9.25 (s, 1H), 7.78 (d, J=1.8 Hz, 1H), 7.61 (d, J=8.4 Hz, 1H), 7.31 (dd, J=8.1, 1.8 Hz, 1H), 4.26 (t, J=5.1 Hz, 4H), 3.06 (m, 4H). MS m/z: 333 (M+H+).
The HCl salt of the title compound was prepared as described in Example 166, except that 1,4-diazabicyclo[4.3.0]nonane was substituted for N-methylpiperazine in the last step. 1H NMR (300 MHz, CD3OD) δ: 9.85 (s, 1H), 8.04 (d, J=2.4 Hz, 1H), 7.59 (d, J=8.7 Hz, 1H), 7.45 (dd, J=9.0, 2.4 Hz, 1H), 5.52 (br, 1H), 4.57 (br 1H), 3.60 (br, 6H), 2.35-1.90 (m, 5H). MS: m/z 329 (M+H+).
The HCl salt of the title compound was prepared as described in Example 157, except that piperazine was substituted for N-methylpiperazine in step 9 of that route. 1H NMR (300 MHz, D2O) δ: 8.60 (s, 1H), 8.20 (s, 1H), 7.79 (d, J=8.7 Hz, 1H), 7.69 (d, J=8.7 Hz, 1H), 4.60 (br, 4H), 3.54 (t, J=4.8 Hz, 4H). MS m/z: 322 (M+H+).
The title compound was prepared as described in Example 152, except that 5-bromoindole was substituted for 5-chloroindole as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 8.56 (s, 1H), 8.13 (d, J=2.1 Hz, 1H), 7.54 (d, J=8.7 Hz, 1H), 7.45 (dd, J=8.7, 2.1 Hz, 1H), 4.22 (m, 4H), 2.64 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 346 (M+H+).
The HCl salt of the title compound was prepared as described in Example 153, except that 5-bromoindole was substituted for 5-chloroindole as the starting material of that route. 1H NMR (300 MHz, D2O) δ: 8.46 (s, 1H), 7.83 (s, 1H), 7.45 (s, 2H), 4.65 (br, 4H), 3.54 (m, 4H). MS m/z: 332 (M+H+).
The title compound was prepared as described in Example 150, except that 5-bromoindole was substituted for 5-chloroindole as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 8.44 (s, 1H), 8.00 (d, J=2.1 Hz, 1H), 7.46 (d, J=4.8 Hz, 1H), 7.43 (dd, J=4.8, 2.1 Hz, 1H), 4.27 (t, J=5.1 Hz, 4H), 4.18 (s, 3H), 2.61 (t, J=5.1 Hz, 4H), 2.35 (s, 3H). MS m/z: 360 (M+H+).
The title compound was prepared as described in Example 234, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 8.42 (s, 1H), 7.98 (d, J=2.1 Hz, 1H), 7.44 (d, J=4.8 Hz, 1H), 7.43 (dd, J=4.8, 2.1 Hz, 1H), 4.22 (t, J=5.1 Hz, 4H), 4.17 (s, 3H), 2.98 (t, J=5.1 Hz, 4H). MS m/z: 346 (M+H+).
A 1 L round bottom flask was charged with 2-fluoro-3-(trifluoromethyl)aniline (25 g, 0.14 mol), di-tert-butyl dicarbonate (91 g, 0.42 mol), 4-(dimethylamino)pyridine (1.7 g, 14 mmol) and THF (500 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in EtOAc (500 mL) and washed with brine (100 mL). The organic layer was dried over anhydrous Na2SO4 and then concentrated in vacuo, to afford 43 g (81%) of the product as white oil.
A 1 L round bottom flask was charged with tert-butyl {(tert-butoxy)-N-[2-fluoro-3-(trifluoromethyl)phenyl]carbonylamino}formate (43 g, 0.11 mol), K2CO3 (31 g, 0.22 mol) and MeOH (300 mL). The resulting mixture was stirred at reflux for 2 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:30). Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in EtOAc (200 mL) and washed with 0.5 N HCl (50 mL). The organic layer was dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 2% EtOAc in petroleum ether, to afford 16 g (52%) of the product as white oil. 1H NMR (300 MHz, CDCl3) δ: 8.34-8.29 (m, 1H), 7.25-7.16 (m, 2H), 6.78 (s, 1H), 1.53 (s, 9H).
A 1 L 3-necked round bottom flask was charged with tert-butyl 2-fluoro-3-(trifluoromethyl)phenylcarbamate (10 g, 35.8 mmol) and dry THF (300 mL). To the above was added dropwise t-BuLi solution (1.3 M, 55.2 mL, 71.8 mmol) at −70° C. The resulting mixture was stirred at −50° C. for 1 h, followed by dropwise addition of a solution of CBr4 (13.1 g, 39.5 mmol) in THF (50 mL) at −70° C. The reaction mixture was stirred at room temperature for further 1 h. It was then carefully mixed with ice water and extracted with Et2O. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 2-5% EtOAc in petroleum ether, to afford 9.4 g (73%) of the product as yellow solid. 1H NMR (300 MHz, CDCl3) δ: 7.49 (d, J=8.4 Hz, 1H), 7.35 (t, J=8.4 Hz, 1H), 6.07 (s, 1H), 1.50 (s, 9H).
A 1 L 3-necked round bottom flask was charged with tert-butyl 6-bromo-2-fluoro-3-(trifluoromethyl)phenylcarbamate (9.4 g, 26 mmol), trifluoroacetic acid (40 mL) and CH2Cl2 (50 mL). The resulting mixture was stirred at room temperature for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in EtOAc (200 mL) and washed with brine (50 mL). The organic layer was dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 5% EtOAc in petroleum ether, to afford 6.2 g (91%) of the product.
A 200 mL pressure tube was charged with 6-bromo-2-fluoro-3-(trifluoromethyl)aniline (7.0 g, 27 mmol), Cu2O (1.0 g, 7.0 mmol), CuCl (1.0 g, 10 mmol) and saturated methanolic ammonia solution (100 mL). The tube was sealed and the resulting mixture was stirred at 150° C. overnight. Work-up: the reaction mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 30% EtOAc in petroleum ether, to afford 2.8 g (53%) of the product. 1H NMR (300 MHz, CDCl3) δ: 6.91 (t, J=7.5 Hz, 1H), 6.48 (d, J=8.4 Hz, 1H), 3.80 (s, 2H), 3.36 (s, 2H).
The title compound was prepared as described in Example 23, except that 3-fluoro-4-(trifluoromethyl)benzene-1,2-diamine was substituted for 4-(trifluoromethyl)benzene-1,2-diamine in step 1 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.40 (d, J=2.4 Hz, 1H), 7.63 (t, J=8.1 Hz, 1H), 7.48 (d, J=10.2 Hz, 1H), 4.58 (br, 4H), 2.62 (t, J=4.8 Hz, 4H), 2.38 (s, 3H). MS m/z: 355 (M+H+).
A 250 mL round bottom flask was charged with 1-bromo-2,5-difluoro-4-nitrobenzene (5.0 g, 21 mmol) and ethanol (70 mL). To the solution was added dropwise hydrazine hydrate (2.1 mL, 42 mmol) at 0° C. The resulting mixture was stirred overnight at room temperature. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:3). Work-up: the reaction mixture was partitioned between EtOAc (200 mL) and brine (100 mL). The organic layer was dried over anhydrous Na2SO4 then concentrated in vacuo to afford 5.2 g (quantitative yield) of the product, which was fairly pure and used in next step without further purification.
The title compound was prepared as described in Example 165 steps 2-7, except that (5-bromo-4-fluoro-2-nitrophenyl)hydrazine was substituted for 5-chloro-2-nitrophenylhydrazine in step 2 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.36 (d, J=7.2 Hz, 1H), 7.40 (d, J=9.6 Hz, 1H), 4.39 (br, 4H), 2.63 (s, 3H), 2.58 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 379 (M+H+).
The title compound was prepared as described in Example 237, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.35 (d, J=6.9 Hz, 1H), 7.39 (d, J=9.6 Hz, 1H), 4.34 (t, J=5.1 Hz, 4H), 3.05 (t, J=5.1 Hz, 4H), 2.63 (s, 3H). MS m/z: 365 (M+H+).
The title compound was prepared as described in Example 237, except that 2,5-difluoro-4-nitrotoluene was substituted for 1-bromo-2,5-difluoro-4-nitrobenzene as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 7.93 (d, J=7.2 Hz, 1H), 7.26 (d, J=10.8 Hz, 1H), 4.30 (t, J=4.8 Hz, 4H), 2.62 (t, J=5.1 Hz, 4H), 2.58 (s, 3H), 2.39 (d, J=1.5 Hz, 3H), 2.36 (s, 3H). MS m/z: 315 (M+H+).
The title compound was prepared as described in Example 239, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 7.89 (d, J=7.5 Hz, 1H), 7.23 (d, J=10.8 Hz, 1H), 4.31 (t, J=4.8 Hz, 4H), 3.09 (t, J=5.4 Hz, 4H), 2.57 (s, 3H), 2.38 (d, J=2.1 Hz, 3H). MS m/z: 301 (M+H+).
The title compound was prepared as described in Example 237, except that 1-bromo-3-fluoro-4-nitrobenzene was substituted for 1-bromo-2,5-difluoro-4-nitrobenzene as the starting material of that route. 1H NMR (300 MHz, CDCl3) δ: 8.33 (m, 1H), 7.55 (m, 2H), 4.37 (t, J=4.8 Hz, 4H), 2.64 (s, 3H), 2.60 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 361 (M+H+).
The title compound was prepared as described in Example 241, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CDCl3) δ: 8.33 (m, 1H), 7.54 (m, 2H), 4.32 (t, J=5.1 Hz, 4H), 3.06 (t, J=4.8 Hz, 4H), 2.64 (s, 3H). MS m/z: 347 (M+H+).
A 500 mL round bottom flask was charged with 5-chloro-2-nitroaniline (14.8 g, 0.086 mol), concentrated HCl (40 mL), ethanol (20 mL) and water (20 mL). To the above was added dropwise a solution of NaNO2 (6.5 g, 0.094 mol) in water (50 mL) at 0-5° C., followed by the addition of a cold solution of ethyl 2-chloroacetoacetate (12.7 g, 0.086 mol) and sodium acetate (8.08 g, 0.097 mol) in ethanol (370 mL) and water (40 mL). The reaction mixture was stirred at −5° C. for 4 h. Work up: The reaction was quenched with water (1.5 L) and stirred for further 2 h. The solid was collected and recrystallized from ethanol to give 20.5 g (78%) of the product. 1H NMR (300 MHz, CDCl3) δ: 11.39 (s, 1H), 8.20 (d, J=9.0 Hz, 1H), 7.95 (d, J=1.8 Hz, 1H), 7.06-7.02 (m, 1H), 4.48-4.40 (m, 2H), 1.46-1.41 (m, 3H).
A 500 mL round bottom flask was charged with (Z)-ethyl 2-chloro-2-(2-(5-chloro-2-nitrophenyl)hydrazono)acetate (20.5 g, 0.067 mol) and THF (250 mL). Ammonia gas was introduced by bubbling through the reaction solution for 4 h. The reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:4, Rf=0.5). Work up: The reaction solution was concentrated in vacuo to give 19.1 g (quantitative yield) of the product. MS m/z: 286 (M+H+).
The title compound was prepared as described in Example 164 steps 3-5, except that (Z)-ethyl 2-amino-2-(2-(5-chloro-2-nitrophenyl)hydrazono)acetate was substituted for ((1Z)-2-amino-1-azaprop-1-enyl)(5-chloro-2-nitrophenyl)amine in step 3 of that route. MS m/z: 293 (M+H+).
A 500 mL round bottom flask was charged with ethyl 8-chloro-4-oxo-4,5-dihydro-[1,2,4]triazolo[1,5-a]quinoxaline-2-carboxylate (1.5 g, 5.1 mmol), NaOH (4.0 g, 0.1 mol), water (85 mL) and ethanol (85 mL). The resulting mixture was heated at reflux for 3 h. The reaction progress was monitored by LC-MS. Work up: the solid was collected and dissolved in water (20 mL). To the aqueous solution was added dropwise 6N HCl (2 mL). The precipitate was collected by filtration, washed with water and dried, to afford 1.35 g (99%) of the product. 1H NMR (300 MHz, DMSO-d6) δ: 12.52 (s, 1H), 8.07 (s, 1H), 7.60 (d, J=8.1 Hz, 1H), 7.46 (d, J=8.1 Hz, 1H). MS m/z: 263 (M−H+).
A 50 mL round bottom flask was charged with 8-chloro-4-oxo-4,5-dihydro-[1,2,4]triazolo[1,5-a]quinoxaline-2-carboxylic acid (1.35 g, 5.1 mmol), Cu2O (20 mg, 0.13 mmol) and HO(CH2CH2O)2H (30 mL). The resulting mixture was heated at 135° C. overnight. The reaction progress was monitored by LC-MS. Work up: the solid was collected by filtration, washed with 0.5 M aqueous NaHCO3 (10 mL) and then with a few drops of ammonia/ammonium chloride buffer (PH 9), and dried, to afford 0.84 g (75%) of the product. MS m/z: 219 (M−H+).
The title compound was prepared as described in Example 164 steps 6-7, except that 8-chloro-[1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one was substituted for 8-chloro-2-methyl-[1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one in step 6 and N-methylpiperazine for piperazine in step 7 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.37 (s, 1H), 8.23 (d, J=2.1 Hz, 1H), 7.65 (d, J=9.0 Hz, 1H), 7.44 (dd, J=9.0, 2.1 Hz, 1H), 4.38 (t, J=5.0 Hz, 4H), 2.60 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared as described in Example 164 steps 6-7, except that ethyl 8-chloro-4-oxo-4,5-dihydro-[1,2,4]triazolo[1,5-a]quinoxaline-2-carboxylate (prepared as described in Example 243, steps 1-5) was substituted for 8-chloro-2-methyl-[1,2,4]triazolo[1,5-a]quinoxalin-4(5H)-one in step 6 and N-methylpiperazine for piperazine in step 7 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.36 (d, J=2.1 Hz, 1H), 7.65 (d, J=9.0 Hz, 1H), 7.48 (dd, J=9.0, 2.1 Hz, 1H), 4.58 (q, J=7.2 Hz, 2H), 4.41 (br, 4H), 2.60 (t, J=5.1 Hz, 4H), 2.37 (s, 3H), 1.50 (t, J=7.2 Hz, 3H). MS m/z: 375 (M+H+).
The title compound was prepared as described in Example 111, except that 1,4-diazabicyclo[4.3.0]nonane was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.12 (d, J=2.4 Hz, 1H), 7.70 (dd, J=8.7, 2.4 Hz, 1H), 7.63 (d, J=8.7 Hz, 1H), 4.90 (m, 2H), 3.28-2.99 (m, 3H), 2.85 (m, 1H), 2.52 (s, 3H), 2.34-2.27 (m, 1H), 2.14-2.05 (m, 2H), 1.83-1.64 (m, 3H), 1.40-1.35 (m, 1H). MS m/z: 343 (M+H+).
The title compound was prepared as described in Example 122, except that 4-chloro-2-fluoroaniline was substituted for 3-chloro-4-(trifluoromethyl)aniline as the starting material of that route. 1H NMR (300 MHz, CDCl3) δ: 8.08 (dd, J=2.1, 1.2 Hz, 1H), 7.37 (dd, J=10.2, 2.4 Hz, 1H), 4.17 (t, J=4.8 Hz, 4H), 2.64 (t, J=5.4 Hz, 4H), 2.64 (s, 3H), 2.38 (s, 3H). MS m/z: 335 (M+H+).
The title compound was prepared as described in Example 246, except that piperazine was substituted for N-methylpiperazine in the last step of that route. 1H NMR (300 MHz, CD3OD) δ: 7.92 (dd, J=2.4, 1.8 Hz, 1H), 7.46 (dd, J=10.2, 2.4 Hz, 1H), 4.12 (t, J=5.1 Hz, 4H), 3.09 (t, J=5.1 Hz, 4H), 2.59 (s, 3H). MS m/z: 321 (M+H+).
The title compound was prepared as described in Example 122, except that 4-bromo-2-fluoroaniline was substituted for 3-chloro-4-(trifluoromethyl)aniline as the starting material of that route. 1H NMR (300 MHz, CDCl3) δ: 8.25 (dd, J=2.1, 1.5 Hz, 1H), 7.50 (dd, J=9.9, 2.1 Hz, 1H), 4.23 (t, J=4.8 Hz, 4H), 2.72 (t, J=5.1 Hz, 4H), 2.63 (s, 3H), 2.43 (s, 3H). MS m/z: 379 (M+H+).
A 20 mL microwave reaction tube was charged with 3-chloro-2-cyanopyridine (1.00 g, 7.2 mmol), 4-chloro-2-fluorophenylboronic acid (1.51 g, 8.7 mmol), Pd(PPh3)4 (417 mg, 0.36 mmol), K3PO4 (3.8 g, 18 mmol) and DMF (15 mL). After O2 was purged by bubbling N2 into the reaction solution, the tube was sealed and heated at 150° C. for 0.5 h in a Biotage microwave reactor. Work-up: the reaction mixture was poured into water (150 mL) and extracted with EtOAc (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 50% CH2Cl2 in petroleum ether, to afford 0.53 g (32%) of the product as white solids. 1H NMR (300 MHz, CDCl3) δ: 8.73 (dd, J=4.8, 1.6 Hz, 1H), 7.85 (dt, J=8.0, 1.4 Hz, 1H), 7.60 (dd, J=8.0, 4.7 Hz, 1H), 7.41 (t, J=8.2 Hz, 1H), 7.33-7.26 (m, 2H).
A 20 mL microwave reaction tube was charged with 3-(4-chloro-2-fluorophenyl)picolinonitrile (0.44 g, 1.9 mmol), KOH (0.53 g, 9.5 mol) and methanol (10 mL). The tube was sealed and heated at 120° C. for 1 h in a Biotage microwave reactor. Work-up: the reaction mixture was poured into water (100 mL) and extracted with EtOAc (100 mL×4). The combined organic layers were dried over anhydrous Na2SO4 and then concentrated in vacuo, to afford 0.24 g (55%) of the product as white solids. 1H NMR (300 MHz, DMSO-d6) δ: 11.94 (br, 1H), 8.93-8.87 (m, 2H), 8.41 (d, J=8.8 Hz, 1H), 7.83 (dd, J=8.2, 4.4 Hz, 1H), 7.39 (d, J=2.0 Hz, 1H), 7.30 (dd, J=8.8, 2.0 Hz, 1H).
A 100 mL round bottom flask was charged with 8-chlorobenzo[f][1,7]naphthyridin-5(6H)-one (0.24 g, 1.0 mmol) and POCl3 (50 mL). The resulting mixture was refluxed for 3 h and then concentrated in vacuo. The residue was carefully diluted with saturated aqueous NaHCO3 (150 mL) and extracted with EtOAc (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 0-2% CH3OH in CH2Cl2, to afford 0.20 g (77%) of the product as white solids. 1H NMR (300 MHz, CDCl3) δ: 9.16 (dd, J=4.4, 1.5 Hz, 1H), 8.86 (dd, J=8.5, 1.5 Hz, 1H), 8.40 (d, J=8.8 Hz, 1H), 8.13 (d, J=2.2 Hz, 1H), 7.85 (dd, J=8.5, 4.4 Hz, 1H), 7.69 (dd, J=8.8, 2.2 Hz, 1H).
A 20 mL microwave reaction tube was charged with 5,8-dichlorobenzo[f][1,7]naphthyridine (0.24 g, 0.96 mmol), N-methylpiperazine (0.33 mL, 3.0 mmol) and THF (10 mL). The tube was sealed and heated at 90° C. for 1 h in a Biotage microwave reactor. Work-up: the reaction mixture was poured into saturated aqueous NaHCO3 (60 mL) and extracted with CH2Cl2 (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with CH2Cl2 (saturated with NH3), to afford 0.26 g (86%) of the product as off-white solids. 1H NMR (300 MHz, CDCl3) δ: 8.91 (dd, J=4.3, 1.7 Hz, 1H), 8.74 (dd, J=8.4, 1.7 Hz, 1H), 8.19 (d, J=8.7 Hz, 1H), 7.84 (d, J=2.1 Hz, 1H), 7.66 (dd, J=8.4, 4.3 Hz, 1H), 7.36 (dd, J=8.7, 2.1 Hz, 1H), 4.13 (t, J=4.7 Hz, 4H), 2.70 (t, J=5.0 Hz, 4H), 2.39 (s, 3H). MS: m/z 313 (M+H+).
The title compound was prepared as described in Example 229, except that 2-chloro-3-cyanopyrazine was substituted for 3-chloro-2-cyanopyridine as the starting material. 1H NMR (300 MHz, CDCl3) δ: 8.96 (d, J=1.9 Hz, 1H), 8.82 (d, J=1.9 Hz, 1H), 8.71 (d, J=8.7 Hz, 1H), 7.80 (d, J=2.1 Hz, 1H), 7.39 (dd, J=8.7, 2.1 Hz, 1H), 4.14 (t, J=5.0 Hz, 4H), 2.68 (t, J=5.0 Hz, 4H), 2.39 (s, 3H). MS: m/z 314 (M+H+).
A 50 mL round bottom flask was charged with ethyl 3,3-diethoxypropionate (1.7 g, 8.9 mmol), LiOH (0.75 g, 18 mmol), THF (5 mL) and H2O (10 mL). The mixture was heated at 80° C. for 1 h then cooled to room temperature and acidified with concentrated HCl. The product was extracted with EtOAc. The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 1.43 g of the product as bright yellow oil. It was then treated with thionyl chloride (7 mL) at 80° C. for 1 h. Evaporation of the solvent provided the title compound as yellow oil with quantitative yield, which was used in next step without further purification.
A 50 mL round bottom flask was charged with 3-chloroaniline (1.12 g, 8.80 mmol), pyridine (1.5 mL, 8.8 mmol) and dichloromethane (15 mL). To the mixture was added dropwise a solution of 3-ethoxyacryloyl chloride (2.2 g, 16 mmol) in dichloromethane (5 mL). The resulting solution was stirred overnight at room temperature. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:4). Work-up: the reaction mixture was diluted with EtOAc (50 mL). The organic solution was washed with brine (40 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 1.5 g (74%) of the product as light yellow crystals.
A 50 mL round bottom flask was charged with concentrated sulfuric acid (15 mL). To the above was added in portions N-(3-chlorophenyl)-3-ethoxyacrylamide (1.5 g, 13 mmol). The resulting mixture was stirred at room temperature for 1.5 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1). Work-up: the reaction mixture was poured into ice water and stirred for 15 min. The white precipitate was collected by filtration and washed with more water. It was recrystallized from acetic acid, to afford 0.94 g (40%) of the product as white crystals.
A 50 mL round bottom flask was charged with 7-chloroquinolin-2(1H)-one (0.37 g, 2.1 mmol) and DMF (15 mL). To the solution was added N-bromosuccinimide (0.56 g, 3.1 mmol). The resulting mixture was heated at 60° C. for 3 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:1). Work-up: the reaction mixture was poured into water and extracted with EtOAc. The organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 50% EtOAc in petroleum ether, to afford 0.38 g (68%) of the product as light yellow crystals.
A 50 mL round bottom flask was charged with 3-bromo-7-chloroquinolin-2(1H)-one (0.40 g, 1.6 mmol) and phosphorus oxychloride (10 mL). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: after the reaction mixture was cooled to room temperature, it was cautiously poured into ice water. The precipitate was collected by filtration and re-dissolved in EtOAc (20 mL). The organic solution was washed with brine (20 mL), dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 0.31 g (72%) of the product as white solid.
A 50 mL round bottom flask was charged with 3-bromo-2,7-dichloroquinoline (0.31 g, 1.1 mmol) and EtOH (10 mL). To the solution was added dropwise hydrazine hydrate (0.10 g, 2.8 mmol). The solution was heated at 60° C. overnight. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the reaction mixture was filtered. The filtrate was concentrated then petroleum ether (20 mL) was added. The resulting solid was collected by filtration and dried, to afford 0.23 g (77%) of the product as light yellow solid.
A 50 mL round bottom flask was charged with 3-bromo-7-chloro-2-hydrazinylquinoline (0.34 g, 1.3 mmol) and triethyl orthoformate (10 mL). The resulting mixture was stirred at 130° C. for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the resulting solid was collected by filtration, washed with EtOH (10 mL×2) and dried, to afford 0.27 g (78%) of the product as light yellow powder.
A 50 mL round bottom flask was charged with 4-bromo-8-chloro-[1,2,4]triazolo[4,3-a]quinoline (0.15 g, 0.53 mmol), N-methylpiperazine (0.11 g, 1.1 mmol), CuI (0.20 g, 1.1 mmol), L-proline (0.061 g, 0.53 mmol), K3PO4 (0.23 g, 1.1 mmol) and DMSO (5 mL). The resulting mixture was heated at 120° C. for 1 h under N2 atmosphere. Work-up: the reaction mixture was poured into brine (20 mL) and extracted with CH2Cl2 (30 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash chromatography on silica gel with 5% MeOH in CH2Cl2, to afford 30 mg (21%) of the product as light yellow crystals. 1H NMR (300 MHz, CDCl3) δ: 9.15 (s, 1H), 7.84 (d, J=1.8 Hz, 1H), 7.57 (d, J=8.4 Hz, 1H), 7.38 (dd, J=8.4, 1.8 Hz, 1H), 6.59 (s, 1H), 3.69 (t, J=4.5 Hz, 4H), 2.71 (t, J=5.1 Hz, 4H), 2.39 (s, 3H). MS m/z: 302 (M+H+).
The title compound was prepared as described in Example 166, except that N-BOC-piperazine was substituted for N-methylpiperazine in the last step of that route.
A 250 mL 3-necked round bottom flask was charged with tert-butyl 4-(8-chloroisoxazolo[3,4-c]quinolin-4-yl)piperazine-1-carboxylate (˜7 mmol, crude) and ethanol (100 mL). The reaction mixture was refluxed for 6 h and NaBH4 (0.89 g×4, 94 mmol) was added in portions. It was cooled to room temperature and poured into 0.2 M HCl (150 mL). The resulting mixture was stirred for 10 min and extracted with ethyl acetate (100 mL×3). The combined organic layers were washed with saturated aqueous NaHCO3 (100 mL) and brine (100 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 20-60% ethyl acetate in petroleum ether, to afford 1.0 g (36%) of the product as light-brown solid. 1H NMR (300 MHz, CDCl3) δ: 7.73 (d, J=1.8 Hz, 1H), 7.72 (d, J=8.7 Hz, 1H), 7.30 (dd, J=8.7, 2.1 Hz, 1H), 5.03 (s, 2H), 4.70 (br, 2H), 3.61 (t, J=5.2 Hz, 4H), 3.19 (t, J=5.2 Hz, 4H), 1.48 (s, 9H).
A 250 mL round bottom flask was charged with tert-butyl 4-(3-amino-6-chloro-4-(hydroxymethyl)quinolin-2-yl)piperazine-1-carboxylate (1.0 g, 2.5 mmol), MnO2 (5.5 g, freshly prepared from MnSO4 and KMnO4, 63 mmol) and CHCl3 (100 mL). The suspension was stirred for 20 h at 40° C. under N2. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the mixture was filtered through Celite and the solids were washed with EtOAc (500 mL). The combined solutions were concentrated in vacuo and the residue was purified by flash column chromatography on silica gel with 10-20% ethyl acetate in petroleum ether, to afford 0.78 g (78%) of the product as orange solid. 1H NMR (300 MHz, CDCl3) δ: 10.78 (s, 1H), 8.19 (s, 1H), 7.87 (d, J=8.6 Hz, 1H), 7.38 (d, J=8.6 Hz, 1H), 3.67 (br, 4H), 3.28 (br, 4H), 1.49 (s, 9H).
Each of two 20 mL microwave reaction tubes was charged with tert-butyl 4-(3-amino-6-chloro-4-formylquinolin-2-yl)piperazine-1-carboxylate (0.39 g, 1.0 mmol), formamide (15 mL) and acetic acid (2 mL). Both tubes were sealed and heated at 100° C. for 4 h in a Biotage microwave reactor. Work-up: the reaction mixtures were combined and poured into saturated aqueous NaHCO3 (150 mL) and extracted with ethyl aceate (150 mL×2). The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 4-20% ethyl acetate in CH2Cl2, to afford 0.31 g (39%) of the product as light-brown solid. 1H NMR (300 MHz, CDCl3) δ: 9.96 (s, 1H), 9.46 (s, 1H), 8.35 (d, J=2.1 Hz, 1H), 7.78 (d, J=8.7 Hz, 1H), 7.62 (dd, J=8.7, 2.1 Hz, 1H), 4.08 (t, J=5.1 Hz, 4H), 3.69 (t, J=5.1 Hz, 4H), 1.50 (s, 9H).
A 100 mL round bottom flask was charged with tert-butyl 4-(9-chloropyrimido[4,5-c]quinolin-5-yl)piperazine-1-carboxylate (0.30 g, 0.75 mmol) and THF (25 mL). To the solution was added concentrated HCl (5 mL) and the resulting slurry was refluxed for 20 min. The reaction mixture was then allowed to cool to room temperature and neutralized with Na2CO3. It was diluted with water and extracted with CH2Cl2 (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with CH2Cl2, to afford 0.11 g (49%) of the product as yellow solid. 1H NMR (300 MHz, CD3OD/CDCl3) δ: 10.04 (s, 1H), 9.40 (s, 1H), 8.47 (d, J=2.2 Hz, 1H), 7.75 (d, J=9.0 Hz, 1H), 7.60 (dd, J=9.0, 2.2 Hz, 1H), 4.06 (t, J=5.1 Hz, 4H), 3.09 (t, J=5.1 Hz, 4H). MS m/z: 300 (M+H+).
The title compound was prepared as described in Example 252, except that N-methylpiperazine was substituted for N-BOC-piperazine in step 8 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.91 (s, 1H), 9.44 (s, 1H), 8.29 (d, J=0.6 Hz, 1H), 7.74 (d, J=8.4 Hz, 1H), 7.58 (dd, J=8.7, 1.2 Hz, 1H), 4.21 (br, 4H), 2.81 (br, 4H), 2.47 (s, 3H). MS m/z: 314 (M+H+).
A 1 L 3-necked round bottom flask was charged with ethyl nitroacetate (16 mL, 144 mmol), Et3N (20 mL, 144 mmol) and anhydrous THF (400 mL). To the above was added dropwise a solution of 6-chloro-1H-benzo[d]1,3-oxazine-2,4-dione (19 g, 96 mmol) in THF (100 mL). The resulting solution was heated at 55° C. overnight then concentrated under reduced pressure. The residue was washed with Et2O then dissolved in water and acidified with 6 M HCl. The precipitate was collected by filtration, washed with H2O and dried, to afford 16 g (90%) of the product as yellow solid. 1H NMR (300 MHz, DMSO-d6) δ: 11.85 (br, 1H), 8.00 (d, J=2.7 Hz, 1H), 7.64 (dd, J=8.4, 2.1 Hz, 1H), 7.31 (d, J=9.0 Hz, 1H).
A 100 mL round bottom flask was charged with 6-chloro-4-hydroxy-3-nitroquinolin-2(1H)-one (5.0 g, 21 mmol) and pyridine (5 mL). To the mixture was added dropwise POCl3 (25 mL) over a period of 1 h while keeping the temperature below 50° C. The suspension was heated at reflux for 2.5 h then cooled to room temperature and concentrated in vacuo. The residue was poured into saturated aqueous NaHCO3 and extracted with EtOAc. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash chromatography on silica gel with 2.5% EtOAc in petroleum ether, to afford 3.5 g (70%) of the product as white solid.
A 250 mL round bottom flask was charged with 2,4,6-trichloro-3-nitroquinoline (3.5 g, 13 mmol) and ammonia in 1.4-dioxane solution (150 mL). The mixture was heated at 30° C. for 4 h then concentrated in vacuo. The residue was poured into saturated aqueous NaHCO3 and extracted with EtOAc. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash chromatography on silica gel with 20% EtOAc in petroleum ether, to afford 3.0 g (86%) of the product as white solid. MS m/z: 258 (M+H+).
A 20 mL microwave reaction tube was charged with 2,6-dichloro-3-nitroquinolin-4-amine (1.0 g, 3.9 mmol), N-methylpiperazine (0.78 g, 7.8 mmol) and EtOH (15 mL). The resulting solution was heated at 130° C. for 1 h in a Biotage microwave reactor. The solvent was evaporated and the residue was purified by flash chromatography on silica gel with 10% MeOH in CH2Cl2, to afford 0.8 g (80%) of the product as white solid. MS m/z: 321 (M+H+).
A 250 mL round bottom flask was charged with 6-chloro-2-(4-methylpiperazin-1-yl)-3-nitroquinolin-4-amine (3.2 g, 10 mmol), Na2S2O4 (8.0 g, 45 mmol), H2O (45 mL) and EtOH (90 mL). The mixture was heated at reflux for 1 h. Work-up: the solvent was evaporated. The residue was suspended in triethylamine (15 mL) and ethyl acetate (300 mL), and then filtered. The filtrate was concentrated in vacuo, to afford 2.3 g (72%) of the product as pale-red solid. MS m/z: 292 (M+H+).
A 50 mL round bottom flask was charged with 6-chloro-2-(4-methylpiperazin-1-yl)quinoline-3,4-diamine (0.30 g, 1.0 mmol) and CH3COOH (10 mL). To the above was added dropwise a solution of NaNO2 (0.10 g, 1.5 mmol) in water (1 mL) at 10° C. The resulting mixture was stirred at 10° C. for 1 h. Work up: the reaction mixture was neutralized with saturated aqueous Na2CO3 and extracted with ethyl acetate (20 mL×3). The combined organic layers were concentrated in vacuo and the residue was purified by flash column chromatography on silica gel with 10% MeOH in CH2Cl2, to afford 0.10 g (33%) of the product as white solid. 1H NMR (300 MHz, CD3OD) δ: 8.14 (d, J=3.3 Hz, 1H), 7.71 (d, J=8.7 Hz, 1H), 7.51 (dd, J=9.0, 2.4 Hz, 1H), 4.50 (br, 4H), 3.30 (t, J=5.1 Hz, 4H), 2.65 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared as described in Example 254, except that piperizine was substituted for N-methylpiperazine in step 4 of that route. 1H NMR (300 MHz, CD3OD) δ: 7.52 (m, 2H), 7.41 (m, 1H), 4.52 (m, 4H), 3.47 (m, 4H). MS m/z: 289 (M+H+).
The following examples were prepared analogously to previously illustrated examples, as indicated in Table 1, but using appropriate starting materials.
A suspension of 3,4-diaminobenzonitrile (6.28 g, 47.2 mmol, 100 mol %) and oxalic acid (6.15 g, 68.3 mmol, 145 mol %) in 4M aqueous HCl (60 mL) was refluxed for 3 h. The reaction was cooled to room temperature and filtered. The solid was washed with water and azeotropically dried with 3×10 mL portions of toluene to afford the title compound as a light tan solid (8.44 g, 96%). MS, m/z=188 for [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ: 12.21 (s, 1H), 12.02 (s, 1H), 7.51 (dd, J=8 Hz, 2 Hz, 1H), 7.40 (d, J=2 Hz, 1H), 7.22 (d, J=8 Hz, 1H). 13C NMR (100 MHz, DMSO-d6) δ: 155.06 (C), 154.70 (C), 129.79 (C), 126.80 (CH), 126.31 (CH), 118.63 (C), 118.26 (CH), 115.96 (CH). 104.55 (C). Both the 1H and 13C NMR spectra indicated the presence of tautomeric 2,3-dihydroxyquinoxaline-6-carbonitrile (shown below) as a minor component (˜10%).
A suspension of 2,3-dioxo-1,2,3,4-tetrahydroquinoxaline-6-carbonitrile (8.40 g, 44.9 mmol, 100 mol %), SOCl2 (9.2 mL, 15 g, 130 mol %), N,N,-dimethylformamide (0.52 mL, 490 mg, 6.7 mmol, 15 mol %), and 1,2-dichloroethane (60 mL) was refluxed for 5 h, cooled to room temperature, and added to 150 mL of ice water. The precipitate was filtered, washed with water and CH2Cl2, and azeotropically dried with toluene to afford the title compound (10.92 g, >100% nominal yield), which contained residual toluene by 1H NMR analysis. 1H NMR (400 MHz, CDCl3) δ: 8.40 (dd, J=2 Hz, 1 Hz, 1H), 8.15 (dd, J=9 Hz, 1 Hz, 1H), 7.97 (dd, J=9 Hz, 2 Hz, 1H). 13C NMR (100 MHz, CDCl3) δ: 148.57 (C), 147.85 (C), 141.87 (C), 139.66 (C), 133.78 (CH), 132.16 (CH), 129.85 (CH), 117.20 (C), 114.86 (C).
A suspension of 2,3-dichloroquinoxaline-6-carbonitrile (2.73 g, 12.2 mmol, 100 mol %) and tert-butyl piperazine-1-carboxylate (3.25 g, 17.4 mmol, 143 mol %) in absolute ethanol (50 mL) was stirred at room temperature for 18 h. Water (50 mL) was added and the suspension was filtered to afford a solid (2.25 g) and a filtrate. The filtrate was extracted with ethyl acetate (2×100 mL), dried (MgSO4), and filtered. This filtrate was combined with the previously isolated solid and concentrated on silica gel (6.5 g). The residue was chromatographed on silica gel (100 g) eluting with a 10%→25%→40% gradient of ethyl acetate in hexanes to afford the title compound as a yellow solid (2.73 g, 59%). MS, m/z=274 for [M+H—CO2But]+. 1H NMR (400 MHz, DMSO-d6) δ: 8.46 (d, J=2 Hz, 1H), 8.01 (dd, J=8 Hz, 2 Hz, 1H), 7.88 (dd, J=8 Hz, 1 Hz, 1H), 3.64-3.62 (br m, 4H), 3.55-3.53 (br m, 4H), 1.44 (s, 9H). 13C NMR (100 MHz, DMSO-d6) δ: 153.94 (C), 152.92 (C), 142.67 (C), 141.72 (C), 136.26 (C), 132.96 (CH), 131.86 (CH), 127.80 (CH), 118.36 (C), 108.78 (C), 79.16 (C), 48.15 (CH2), 42.5 (br, CH2), 28.03 (CH3).
A suspension of tert-butyl 4-(3-chloro-6-cyanoquinoxalin-2-yl)piperazine-1-carboxylate (1.67 g, 4.47 mmol, 100 mol %), sodium azide (2.46 g, 37.8 mmol, 846 mol %), and absolute ethanol (47 mL) was refluxed for 20 h. After cooling to room temperature, 70 mL of a 1:1 v:v mixture of water:ethyl acetate was added to the suspension, which was then filtered to afford the title compound as an ivory solid (1.00 g, 59%). MS, m/z=281 for [M+H—CO2But]+. 1H NMR (400 MHz, DMSO-d6) δ: 8.83 (d, J=2 Hz, 1H), 8.01 (d, J=8 Hz, 1H), 7.80 (d, J=8 Hz, 1H), 4.4 (br s, 4H), 3.59 (t, J=5 Hz, 4H), 1.46 (s, 9H). 13C NMR (100 MHz, DMSO-d6) δ: 153.54 (C), 144.89 (C), 139.36 (C), 138.04 (C), 131.42 (CH), 126.50 (CH), 120.83 (C), 119.52 (CH), 116.89 (C), 106.45 (C), 79.64 (C), 42.87 (CH2), 27.84 (CH3).
To a 0° C. solution of tert-butyl 4-(8-cyanotetrazolo[1,5-a]quinoxalin-4-yl)piperazine-1-carboxylate (940 mg, 2.47 mmol) in CH2Cl2 (33 mL) was added trifluoroacetic acid (6 mL). After 30 min the reaction was warmed to room temperature. After an additional 2.5 h the reaction was concentrated to afford a viscous orange oil. Addition of warm MeOH (15 mL) afforded a white precipitate, which was filtered to afford the title compound (582 mg, 60%). MS, m/z=281 for [M+H]+of free base. 1H NMR (400 MHz, DMSO-d6) δ: 9.28 (br s, 2H), 8.91 (d, J=2 Hz, 1H), 8.07 (dd, J=8 Hz, 2 Hz, 1H), 7.87 (d, J=8 Hz, 1H), 4.58 (br s, 4H), 3.38 (t, J=5 Hz, 4H). 13C NMR (100 MHz, DMSO-d6) δ: 158.28 (q, J=31 Hz, C), 146.58 (C), 139.89 (C), 139.55 (C), 132.61 (CH), 127.14 (CH), 122.04 (C), 120.54 (CH), 118.12 (C), 106.40 (C), 43.0 (very br, CH2), 42.50 (CH2). Elemental analysis for C13H12N8.CF3CO2H: calculated, C 45.69%, H 3.32%, N 28.42%; found, C 45.56%, H 3.21%, N 28.43%.
To a mixture of 4-(piperazin-1-yl)-4,5-dihydrotetrazolo[1,5-a]quinoxaline-8-carbonitrile trifluoroacetate (192 mg, 0.487 mmol, 100 mol %), 37% aqueous formaldehyde (1.2 mL=440 mg of active formaldehyde, 15 mmol, 3000 mol %), MeOH (3 mL), and CH2Cl2 (3 mL) was added NaCNBH3 (93 mg, 1.5 mmol, 310 mol %). After 2 h aqueous saturated NaHCO3 was added to quench the reaction, and the mixture was extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with saturated aqueous NaCl (2×5 mL), dried (MgSO4), filtered, and concentrated to afford a yellow oil. Addition of warm MeOH (10 mL) precipated the title compound as an ivory solid (78 mg after filtration, 55%). MS, m/z=295 for {M+H]+. 1H NMR (400 MHz, DMSO-d6) δ: 8.81 (d, J=2 Hz, 1H), 8.00 (dd, J=9 Hz, 2 Hz, 1H), 7.79 (d, J=9 Hz, 1H), 4.38 (very br s, 4H), 2.55 (t, J=5 Hz, 4H), 2.27 (s, 3H). 13C NMR (100 MHz, DMSO-d6) δ: 146.36 (C), 140.54 (C), 139.56 (C), 132.38 (CH), 126.75 (C), 121.85 (C), 120.38 (CH), 118.29 (C), 105.35 (C), 54.33 (CH2), 45.50 (CH3).
The title compound was prepared analogously to Example 145. 1H NMR (300 MHz, CDCl3) δ: 8.17 (d, J=6.9 Hz, 1H), 7.42 (d, J=10.8 Hz, 1H), 4.37 (br, 4H), 2.71 (s, 3H), 2.58 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 326 (M+H+).
A 100 mL round bottom flask was charged with 2-amino-6-fluorobenzonitrile (6.8 g, 50 mmol), N-bromosuccinimide (8.9 g, 50 mmol), and DMF (70 mL). The resulting solution was stirred at room temperature for 20 minutes. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:4). Work-up: the reaction mixture was poured into ice water. The white precipitate was collected by filtration and washed with water. It was further purified by recrystallization from 5% MeOH in petroleum ether to afford 8.7 g (61%) of the product. 1H NMR (400 MHz, CDCl3) δ: 7.42 (t, J=8.8 Hz, 1H), 6.45 (d, J=8.8 Hz, 1H), 4.62 (br, 2H).
A 100 mL round bottom flask was charged with 6-amino-3-bromo-2-fluorobenzonitrile (4.3 g, 20 mmol), Na2CO3 (4.2 g, 40 mmol) and ethyl chloroformate (70 mL). The resulting solution was stirred overnight at reflux. Work-up: the reaction mixture was concentrated in vacuo. The residue was re-dissolved in dichloromethane (150 mL) and filtered. The filtrate was concentrated in vacuo, to afford 5.6 g (98%) of the product. MS m/z: 287 (M+H+).
A 100 mL round bottom flask was charged with ethyl (4-bromo-2-cyano-3-fluorophenyl)carbamate (2.87 g, 10 mmol), formic hydrazide (0.72 g, 12 mmol) and 1-methyl-2-pyrrolidone (70 mL). The resulting mixture was heated at 180° C. for 1.5 h. Work-up: the reaction mixture was poured into ice water. The precipitate was collected by filtration and dried to afford 2.8 g (92%) of the product. 1H NMR (400 MHz, DMSO-d6) δ: 12.61 (br, 1H), 8.60 (s, 1H), 7.96 (dd, J=8.8, 8.0 Hz, 1H), 7.21 (d, J=8.8 Hz, 1H). MS m/z: 281 (M−H+).
A 100 mL round bottom flask was charged with 9-bromo-10-fluoro-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one (2.8 g, 9.9 mmol) and POCl3 (50 mL). After N,N-diisopropylethylamine (1.9 g, 15.0 mmol) was added dropwise at 0° C., the resulting solution was heated at reflux for 3 days then concentrated in vacuo. The residue was carefully mixed with saturated aqueous Na2CO3 and extracted with EtOAc. The combined organic layers were dried over anhydrous Na2SO4 and then concentrated in vacuo. It was further purified by recrystallization from 20% EtOAc in petroleum ether to afford 1.66 g (55%) of the product. MS m/z: 299 (M−H+).
A 50 mL round bottom flask was charged with 9-bromo-5-chloro-10-fluoro-[1,2,4]triazolo[1,5-c]quinazoline (301 mg, 1.0 mmol), N-Boc-piperazine (372 mg, 2.0 mmol) and EtOH (5 mL). The resulting solution was stirred at room temperature for 1 h then concentrated in vacuo. The residue was purified by flash column chromatography on silica gel to afford 208 mg (46%) of the product. 1H NMR (400 MHz, CDCl3) δ: 8.43 (s, 1H), 7.78 (dd, J=8.8, 7.6 Hz, 1H), 7.43 (d, J=8.8 Hz, 1H), 4.10 (t, J=4.8 Hz, 4H), 3.68 (t, J=4.8 Hz, 4H), 1.51 (s, 9H). MS m/z: 451 (M+H+).
A 25 mL round bottom flask was charged with tert-butyl 4-(9-bromo-10-fluoro-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)piperazine-1-carboxylate (100 mg, 0.22 mmol), trifluoroacetic acid (2 mL) and dichloromethane (5 mL). The resulting solution was stirred at room temperature for 2 h. Work-up: the reaction solution was neutralized with saturated aqueous Na2CO3 and extracted with dichloromethane (10 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and then concentrated in vacuo, to afford 70 mg (90%) of the product. It was then converted into the corresponding HCl salt by treating with the HCl in EtOAc solution. 1H NMR (400 MHz, D2O) δ: 8.58 (s, 1H), 7.90 (dd, J=8.8, 7.6 Hz, 1H), 7.43 (d, J=8.8 Hz, 1H), 4.27 (t, J=5.2 Hz, 4H), 3.57 (t, J=5.2 Hz, 4H). MS m/z: 351 (M+H+).
A 2 L round bottom flask was charged with 3-fluoro-4-(trifluoromethyl)aniline (150 g, 0.84 mol), di-tert-butyl dicarbonate (850 g, 3.89 mol), triethylamine (423 g, 4.19 mol) and THF (1.5 L). The resulting mixture was stirred overnight at reflux. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the reaction mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a 1:100 EtOAc/Petroleum ether, to afford 328 g (quantitative) of the di-Boc protected aniline product.
A 2 L round bottom flask was charged with the above di-Boc protected aniline product (100 g, 0.26 mol), K2CO3 (73 g, 0.53 mol) and MeOH (1 L). The resulting mixture was stirred at room temperature for 1 h. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:20). Work-up: the reaction mixture was filtered. The filtrate was concentrated in vacuo. The solid obtained was rinsed with water, and dried to afford 70 g (97%) of the product. 1H NMR (300 MHz, CDCl3) δ: 7.52-7.43 (m, 2H), 7.03 (m, 1H), 6.68 (br, 1H), 1.52 (s, 9H).
A 2 L 3-necked round bottom flask was charged with tert-butyl (3-fluoro-4-(trifluoromethyl)phenyl)carbamate (90 g, 0.32 mol) and dry THF (500 mL). To the above was added dropwise n-BuLi solution (2.5 M, 0.9 L, 2.25 mol) with the inner temperature kept below −65° C. The resulting mixture was stirred at −78° C. for 1 h, followed by dropwise addition of a solution of I2 (571 g, 2.25 mmol) in dry THF (1.3 L) with the inner temperature kept below −65° C. The reaction mixture was allowed to warm to room temperature and stirred at that temperature overnight. Saturated aqueous NH4Cl (100 mL) was added slowly, followed by the addition of saturated aqueous NaHSO3 (1 L). The mixture was extracted with ethyl acetate (500 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo to remove 90% of the solvent. To the hot residue was added MeOH (300 mL). The precipitate was collected by filtration and dried, to afford 50 g (38%) of the product as a white solid. The remained crude product from the filtrate was purified by flash column chromatography on silica gel, to afford 21 g (16%) more of the product. 1H NMR (300 MHz, CDCl3) δ: 8.06 (d, J=8.7 Hz, 1H), 7.54 (t, J=8.7 Hz, 1H), 7.13 (br, 1H), 1.55 (s, 9H).
A 500 mL round bottom flask was charged with tert-butyl (3-fluoro-2-iodo-4-(trifluoromethyl)phenyl)carbamate (64 g, 0.16 mol), THF (300 mL) and 12 M HCl (80 mL). The resulting mixture was stirred at 60° C. overnight. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:10). Work-up: the solvent was evaporated to dryness, to afford 47 g (97%) of the product as a white solid. 1H NMR (300 MHz, CDCl3) δ: 7.32 (t, J=8.4 Hz, 1H), 6.52 (d, J=8.4 Hz, 1H), 4.61 (br, 2H).
A 500 mL round bottom flask was charged with 3-fluoro-2-iodo-4-(trifluoromethyl)aniline (40 g, 0.13 mol), CuCN (22 g, 0.25 mol), Pd(PPh3)4 (6.6 g, 5.7 mmol) and DMF (200 mL). The resulting mixture was heated at 110° C. overnight. The solvent was evaporated and the residue was purified by flash column chromatography on silica gel, to afford 17 g (63%) of the product as a white solid. MS m/z: 203 (M−H+).
A 1 L round bottom flask was charged with 6-amino-2-fluoro-3-(trifluoromethyl)benzonitrile (17 g, 83 mmol), Na2CO3 (26 g, 250 mmol) and ethyl chloroformate (300 mL). The resulting mixture was heated at reflux for 24 h. Work-up: the reaction mixture was filtered. The filtrate was concentrated in vacuo to remove 90% of the solvent. To the hot residue was added EtOAc (90 mL). The precipitate was collected by filtration and dried, to afford 12 g (52%) of the product as a yellow solid. The remained crude product from the filtrate was purified by flash column chromatography on silica gel, to afford 10 g (43%) more of the product. MS m/z: 275 (M−H+).
A 500 mL round bottom flask was charged with ethyl (2-cyano-3-fluoro-4-(trifluoromethyl)phenyl)carbamate (22 g, 80 mmol), formic hydrazide (7.1 g, 120 mmol) and 1-methyl-2-pyrrolidinone (150 mL). The resulting mixture was heated at 180° C. for 1.5 h. Work-up: the reaction mixture was cooled to room temperature and poured into water (300 mL). The precipitate was collected by filtration, washed with EtOH, and dried, to afford 12 g (55%) of the product as a white solid.
A 500 mL round bottom flask was charged with 10-fluoro-9-(trifluoromethyl)-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one (20 g, 73 mmol) and POCl3 (150 mL). To the above was added dropwise N,N-diisopropylethylamine (25 mL). The resulting mixture was heated at 120° C. overnight. Work-up: the solvent was evaporated. The residue was washed with EtOAc and the solid was collected by filtration and dried, to afford 10 g (47%) of the product. The remained crude product from the filtrate was purified by flash column chromatography on silica gel, to afford 2 g (9%) more of the product.
A 250 mL round bottom flask was charged with 5-chloro-10-fluoro-9-(trifluoromethyl)-[1,2,4]triazolo[1,5-c]quinazoline (10 g, 34 mmol), N-Boc piperizine (8.2 g, 44 mmol), triethylamine (11 g, 0.11 mol) and EtOH (100 mL). The resulting solution was stirred at room temperature for 1 h and a white precipitate was developed. The solid was collected by filtration and dried, to afford 16 g (quantitative) of the product.
A 250 mL round bottom flask was charged with tert-butyl 4-(10-fluoro-9-(trifluoromethyl)-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)piperazine-1-carboxylate (16 g, 34 mmol), dichloromethane (100 mL) and trifluoroacetic acid (40 mL). The resulting solution was stirred at room temperature overnight. Work-up: the solvent was evaporated. The residue was neutralized with saturated aqueous NaHCO3 and extracted with EtOAc (150 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel, to afford 12 g (quantitative) of the product as a white solid. 1H NMR (300 MHz, CD3OD) δ: 8.57 (s, 1H), 7.93 (t, J=8.4 Hz, 1H), 7.64 (d, J=8.4 Hz, 1H), 4.31 (t, J=5.1 Hz, 4H), 3.22 (t, J=5.1 Hz, 4H), MS m/z: 341 (M+H+).
The title compound was prepared as described in Example 419, except that N-methylpiperazine was substituted for N-Boc-piperazine in step 9 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.75 (s, 1H), 7.97 (t, J=8.5 Hz, 1H), 7.59 (d, J=8.5 Hz, 1H), 4.15 (t, J=4.8 Hz, 4H), 2.55 (t, J=4.8 Hz, 4H), 2.25 (s, 3H). MS m/z: 355 (M+H+).
The HCl salt of the title compound was prepared as described in Example 418, except that N-methylpiperazine was substituted for N-Boc-piperazine in step 5 of that route. The compound was converted into the corresponding HCl salt by treatment with HCl/EtOAc. 1H NMR (400 MHz, D2O) δ: 8.53 (s, 1H), 7.78 (t, J=8.8 Hz, 1H), 7.26 (d, J=8.8 Hz, 1H), 4.96 (d, J=14.0 Hz, 2H), 3.79 (d, J=12.8 Hz, 2H), 3.64 (t, J=13.2 Hz, 2H), 3.47 (t, J=11.6 Hz, 2H), 3.06 (s, 3H). MS m/z: 365 (M+H+).
The title compound was prepared as described in Example 419, except that 3-(N-tert-butoxycarbonyl-N-methylamino)azetidine was substituted for N-Boc-piperazine in step 9 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.42 (s, 1H), 7.76 (t, J=8.6 Hz, 1H), 7.35 (d, J=8.6 Hz, 1H), 4.73 (br, 2H), 4.32 (br, 2H), 3.78-3.70 (m, 1H), 2.41 (s, 3H). MS m/z: 341 (M+H+).
The title compound was prepared as described in Example 418, except that 2-amino-4-fluorobenzonitrile was substituted for 2-amino-6-fluorobenzonitrile as the starting material, and 3-(N-tert-butoxycarbonyl-N-methylamino)azetidine for N-Boc-piperazine in step 5 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.49 (d, J=7.5 Hz, 1H), 8.24 (s, 1H), 7.36 (d, J=9.9 Hz, 1H), 4.80-4.74 (m, 2H), 4.33-4.28 (m, 2H), 3.83-3.77 (m, 1H), 2.48 (s, 3H). MS m/z: 351 (M+H+).
The title compound was prepared as described in Example 418, except that 2-amino-5-bromobenzonitrile was substituted for 6-amino-3-bromo-2-fluorobenzonitrile in step 2, and 3-(N-tert-butoxycarbonyl-N-methylamino)azetidine for N-Boc-piperazine in step 5 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.43 (dd, J=2.4, 0.6 Hz, 1H), 8.26 (s, 1H), 7.70 (dd, J=8.8, 2.4 Hz, 1H), 7.52 (dd, J=8.8, 0.6 Hz, 1H), 4.76 (br, 2H), 4.30 (br, 2H), 3.81-3.76 (m, 1H), 2.48 (s, 3H). MS m/z: 333 (M+H+).
The HCl salt of the title compound was prepared as described in Example 419, except that 4-chloro-3-fluoroaniline was substituted for 3-fluoro-4-(trifluoromethyl)aniline as the starting material, N-methylpiperazine for N-Boc-piperazine in Step 9 of that route. 1H NMR (300 MHz, CD3OD) δ: 8.59 (s, 1H), 7.82 (dd, J=9.0, 7.8 Hz, 1H), 7.60 (dd, J=9.0, 1.2 Hz, 1H), 5.30-5.00 (br, 2H), 3.60-3.50 (br, 6H), 3.00 (s, 3H). MS m/z: 321 (M+H+).
The title compound was prepared as described in Example 418, except that 2-amino-5-(trifluoromethyl)benzonitrile was substituted for 6-amino-3-bromo-2-fluorobenzonitrile in Step 2, and 3-(N-tert-butoxycarbonyl-N-methylamino)azetidine for N-Boc-piperazine in Step 5 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.58-8.57 (m, 1H), 8.28 (s, 1H), 7.80 (dd, J=8.7, 1.8 Hz, 1H), 7.70 (d, J=8.7 Hz, 1H), 4.83-4.77 (m, 2H), 4.37-4.31 (m, 2H), 3.83-3.77 (m, 1H), 2.49 (s, 3H). MS m/z: 323 (M+H+).
The title compound was prepared as described in Example 418, except that 2-amino-4-fluoro-5-(trifluoromethyl)benzonitrile (prepared from 3-fluoro-4-(trifluoromethyl)aniline as described in Example 122) was substituted for 6-amino-3-bromo-2-fluorobenzonitrile in step 2, and 3-(N-tert-butoxycarbonyl-N-methylamino)azetidine for N-Boc-piperazine in step 5 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.56 (d, J=7.5 Hz, 1H), 8.26 (s, 1H), 7.36 (d, J=12.0 Hz, 1H), 4.91-4.75 (m, 2H), 4.42-4.25 (m, 2H), 3.90-3.76 (m, 1H), 2.49 (s, 3H). MS m/z: 341 (M+H+).
The title compound was prepared as described in Example 418, except that 2-amino-5-chlorobenzonitrile was substituted for 6-amino-3-bromo-2-fluorobenzonitrile in Step 2, and 3-(N-tert-butoxycarbonyl-N-methylamino)azetidine for N-Boc-piperazine in Step 5 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.28-8.26 (m, 2H), 7.61-7.53 (m, 2H), 4.76 (dd, J=9.6, 7.2 Hz, 2H), 4.30 (dd, J=9.6, 4.8 Hz, 2H), 3.81-3.76 (m, 1H), 2.48 (s, 3H). MS m/z: 289 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 122. 1H NMR (300 MHz, CD3OD) δ: 7.82 (s, 1H), 7.58 (d, J=8.7 Hz, 1H), 7.32 (d, J=8.7 Hz, 1H), 4.94 (d, J=14.7 Hz, 2H), 3.64 (d, J=12.9 Hz, 2H), 3.56-3.46 (m, 2H), 3.35-3.26 (m, 2H), 2.91 (s, 3H), 2.46 (s, 3H). MS m/z: 308 (M+H+).
The title compound was prepared analogously to Example 122. 1H NMR (300 MHz, CDCl3) δ: 8.64 (d, J=7.2 Hz, 1H), 8.33 (s, 1H), 7.39 (d, J=10.5 Hz, 1H), 4.32 (t, J=5.1 Hz, 4H), 2.64 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 312 (M+H+).
The title compound was prepared analogously to Example 97. 1H NMR (300 MHz, D2O) δ: 8.37 (s, 1H), 7.94 (d, J=8.1 Hz, 1H), 7.35 (d, J=11.1 Hz, 1H), 4.84 (d, J=14.4 Hz, 2H), 3.63 (d, J=12.6 Hz, 2H), 3.53-3.43 (m, 2H), 3.32-3.25 (m, 2H), 2.90 (s, 3H). MS m/z: 371 (M+H+).
The title compound was prepared analogously to Example 114. 1H NMR (300 MHz, DMSO-d6) δ: 8.42 (d, J=1.8 Hz, 1H), 7.95 (dd, J=8.4, 1.8 Hz, 1H), 7.76 (d, J=8.4 Hz, 1H), 4.09 (t, J=5.1 Hz, 4H), 2.91 (q, J=7.6 Hz, 2H), 2.55-2.48 (m, 4H), 2.24 (s, 3H), 1.36 (t, J=7.6 Hz, 3H). MS m/z: 365 (M+H+).
The title compound was prepared analogously to Example 122. 1H NMR (300 MHz, CDCl3) δ: 8.68 (d, J=1.8 Hz, 1H), 8.36 (s, 1H), 7.80 (dd, J=8.4, 1.8 Hz, 1H), 7.72 (d, J=8.4 Hz, 1H), 4.30-4.27 (m, 4H), 2.68 (t, J=5.1 Hz, 4H), 2.41 (s, 3H). MS m/z: 294 (M+H+).
The title compound was prepared analogously to Example 97. 1H NMR (300 MHz, CDCl3) δ: 8.31 (s, 1H), 8.11 (dd, J=9.9, 8.4 Hz, 1H), 7.50 (dd, J=11.1, 7.2 Hz, 1H), 4.11 (t, J=4.8 Hz, 4H), 2.65 (t, J=4.8 Hz, 4H), 2.39 (s, 3H). MS m/z: 305 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 97. 1H NMR (300 MHz, DMSO-d6) δ: 10.91 (br, 1H), 8.74 (s, 1H), 8.20 (d, J=8.7 Hz, 1H), 8.13 (d, J=6.6 Hz, 1H), 4.93 (d, J=14.7 Hz, 2H), 3.62-3.57 (m, 4H), 3.30-3.24 (m, 2H), 2.83 (d, J=4.5 Hz, 3H). MS m/z: 365 (M+H+).
The title compound was prepared analogously to Example 127. 1H NMR (300 MHz, CDCl3) δ: 8.41 (s, 1H), 7.52 (dd, J=10.2, 1.5 Hz, 1H), 4.34 (br, 4H), 2.64 (br, 4H), 2.39 (s, 3H), 1.81 (s, 3H). MS m/z: 326 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 122. 1H NMR (400 MHz, D2O) δ: 8.52 (s, 1H), 7.59 (d, J=8.4 Hz, 1H), 7.53 (d, J=6.4 Hz, 1H), 4.87 (d, J=14.0 Hz, 2H), 3.78 (d, J=12.8 Hz, 2H), 3.58 (t, J=12.8 Hz, 2H), 3.47-3.40 (m, 2H), 3.06 (s, 3H). MS m/z: 321 (M+H+).
The HCl salt of the title compound was prepared as described in Example 419, except that 4-chloro-3-fluoroaniline was substituted for 3-fluoro-4-(trifluoromethyl)aniline as the starting material of that route. 1H NMR (300 MHz, D2O) δ: 8.28 (s, 1H), 7.30 (t, J=8.8 Hz, 1H), 6.91 (d, J=8.8 Hz, 1H), 4.06 (t, J=5.1 Hz, 4H), 3.42 (t, J=5.1 Hz, 4H). MS m/z: 307 (M+H+).
The title compound was prepared analogously to Example 122. 1H NMR (300 MHz, DMSO-d6) δ: 8.62 (s, 1H), 8.57 (d, J=1.8 Hz, 1H), 7.96 (dd, J=8.7, 1.8 Hz, 1H), 7.64 (d, J=8.7 Hz, 1H), 4.68 (br, 2H), 4.25 (br, 2H), 3.69-3.61 (m, 1H), 2.29 (s, 3H). MS m/z: 280 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 122. 1H NMR (300 MHz, D2O/DMSO-d6) δ: 8.77 (d, J=6.9 Hz, 1H), 8.67 (s, 1H), 7.70 (d, J=10.5 Hz, 1H), 4.50 (t, J=4.8 Hz, 4H), 3.51 (t, J=4.8 Hz, 4H). MS m/z: 298 (M+H+).
The title compound was prepared as described in Example 122 step 1, except that 2-amino-5-chlorobenzonitrile was substituted for 3-chloro-4-(trifluoromethyl)aniline.
The title compound was prepared as described in Example 92, except that 2-amino-5-chloro-3-iodobenzonitrile was substituted for 2-amino-5-chlorobenzonitrile, ethyl chloroformate for methyl chloroformate in step 1, acetic hydrazide for formic hydrazide in step 2, and 1-methylpiperazine for piperazine in step 4 of that route.
Reference for introducing cyano group: D M Tschaen et al, Synth. Commun. 1994, 24(6), 887-890. The title compound was obtained as the corresponding HCl salt. 1H NMR (300 MHz, D2O) δ: 7.77 (d, J=2.4 Hz, 1H), 7.75 (d, J=2.4 Hz, 1H), 5.09 (d, J=14.7 Hz, 2H), 3.68-3.53 (m, 4H), 3.32-3.23 (m, 2H), 2.92 (s, 3H), 2.52 (s, 3H). MS m/z: 342 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 122. 1H NMR (300 MHz, D2O) δ: 11.33 (br, 1H), 8.69 (s, 1H), 8.28 (s, 1H), 7.98 (s, 1H), 4.91 (d, J=14.4 Hz, 2H), 3.75-3.50 (m, 4H), 3.30-3.20 (m, 2H), 2.81 (d, J=4.5 Hz, 3H), 2.54 (s, 3H). MS m/z: 361 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 97. 1H NMR (300 MHz, D2O) δ: 8.40 (s, 1H), 8.13 (d, J=8.1 Hz, 1H), 7.50 (d, J=11.4 Hz, 1H), 4.15 (t, J=5.1 Hz, 4H), 3.42 (t, J=5.1 Hz, 4H). MS m/z: 357 (M+H+).
The title compound was prepared analogously to Example 118. 1H NMR (300 MHz, CDCl3) δ: 8.32 (dd, J=2.4, 0.6 Hz, 1H), 7.63 (dd, J=8.7, 0.6 Hz, 1H), 7.57 (dd, J=8.7, 2.4 Hz, 1H), 7.28 (dd, J=4.8, 3.0 Hz, 1H), 7.21 (dd, J=3.0, 1.2 Hz, 1H), 7.15 (dd, J=4.8, 1.2 Hz, 1H), 4.31 (s, 2H), 4.11-4.07 (m, 4H), 2.64 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 399 (M+H+).
The title compound was prepared analogously to Example 122. 1H NMR (300 MHz, CD3OD) δ: 8.51-8.48 (m, 1H), 7.88-7.84 (m, 1H), 7.71-7.67 (m, 1H), 4.18 (t, J=5.1 Hz, 4H), 3.03 (t, J=5.1 Hz, 4H), 2.60 (s, 3H). MS m/z: 294 (M+H+).
The title compound was prepared analogously to Example 122. 1H NMR (300 MHz, CD3OD) δ: 8.73 (dd, J=2.1, 0.6 Hz, 1H), 8.57 (s, 1H), 7.99 (dd, J=8.7, 2.1 Hz, 1H), 7.86 (dd, J=8.7, 0.6 Hz, 1H), 4.46 (t, J=5.1 Hz, 4H), 3.46 (t, J=5.1 Hz, 4H). MS m/z: 280 (M+H+).
The title compound was prepared analogously to Example 118. 1H NMR (300 MHz, CDCl3) δ: 8.32 (dd, J=2.4, 0.6 Hz, 1H), 7.63 (dd, J=8.7, 0.6 Hz, 1H), 7.58 (dd, J=8.7, 2.4 Hz, 1H), 7.20 (dd, J=5.1, 1.2 Hz, 1H), 7.04 (dd, J=3.3, 1.2 Hz, 1H), 6.96 (dd, J=5.1, 3.3 Hz, 1H), 4.50 (s, 2H), 4.12-4.08 (m, 4H), 2.65 (t, J=5.1 Hz, 4H), 2.39 (s, 3H). MS m/z: 399 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 97. 1H NMR (300 MHz, DMSO-d6) δ: 9.27 (br, 1H), 8.72 (s, 1H), 8.20 (d, J=8.4 Hz, 1H), 8.11 (d, J=6.6 Hz, 1H), 4.22 (t, J=5.1 Hz, 4H), 3.33 (br, 4H). MS m/z: 351 (M+H+).
The title compound was prepared analogously to Example 97. 1H NMR (300 MHz, CDCl3) δ: 8.31 (s, 1H), 8.11 (dd, J=9.9, 8.7 Hz, 1H), 7.50 (dd, J=11.4, 7.5 Hz, 1H), 4.05 (t, J=5.1 Hz, 4H), 3.11 (t, J=5.1 Hz, 4H). MS m/z: 291 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 122. 1H NMR (400 MHz, D2O) δ: 8.54 (s, 1H), 7.61 (d, J=9.2 Hz, 1H), 7.55 (d, J=6.8 Hz, 1H), 4.22 (t, J=5.0 Hz, 4H), 3.60 (t, J=5.0 Hz, 4H). MS m/z: 307 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 115. 1H NMR (400 MHz, DMSO-d6) δ: 9.58 (s, 2H), 8.50 (s, 1H), 8.03 (dd, J=8.8, 2.4 Hz, 1H), 7.86 (d, J=8.8 Hz, 1H), 4.36-4.33 (m, 4H), 3.33 (br, 4H), 2.94 (q, J=7.6 Hz, 2H), 1.38 (t, J=7.6 Hz, 3H). MS m/z: 351 (M+H+).
The title compound was prepared analogously to Example 119. 1H NMR (300 MHz, CDCl3) δ: 8.32 (dd, J=2.1, 0.6 Hz, 1H), 7.63 (dd, J=9.0, 0.6 Hz, 1H), 7.57 (dd, J=9.0, 2.1 Hz, 1H), 7.28 (dd, J=4.8, 3.0 Hz, 1H), 7.21 (dd, J=3.0, 1.5 Hz, 1H), 7.16 (dd, J=4.8, 1.5 Hz, 1H), 4.31 (s, 2H), 4.04-4.00 (m, 4H), 3.12-3.08 (m, 4H). MS m/z: 385 (M+H+).
The title compound was prepared analogously to Example 119. 1H NMR (300 MHz, CDCl3) δ: 8.33 (dd, J=2.4, 0.6 Hz, 1H), 7.63 (dd, J=8.7, 0.6 Hz, 1H), 7.58 (dd, J=8.7, 2.4 Hz, 1H), 7.20 (dd, J=5.1, 1.2 Hz, 1H), 7.04 (dd, J=3.3, 1.2 Hz, 1H), 6.96 (dd, J=5.1, 3.3 Hz, 1H), 4.50 (s, 2H), 4.05-4.01 (m, 4H), 3.12-3.08 (m, 4H). MS m/z: 385 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 116. 1H NMR (300 MHz, DMSO-d6) δ: 8.25 (d, J=1.8 Hz, 1H), 7.85-7.74 (m, 2H), 3.60 (t, J=7.2 Hz, 2H), 3.42 (br, 8H), 3.08 (br, 2H), 2.87 (s, 6H), 2.76 (s, 3H). MS m/z: 374 (M+H+).
The title compound was prepared analogously to Example 113. 7,7-difluorooctahydropyrrolo[1,2-a]pyrazine was prepared according to WO2008/124083 A2 Example 385. 1H NMR (400 MHz, CDCl3) δ: 8.32 (d, J=2.0 Hz, 1H), 7.65 (d, J=8.8 Hz, 1H), 7.60 (dd, J=8.8, 2.0 Hz, 1H), 5.04-4.97 (m, 2H), 3.31-3.52 (m, 2H), 3.14-3.00 (m, 2H), 2.74-2.56 (m, 3H), 2.65 (s, 3H), 2.43-2.38 (m, 1H), 2.12-2.04 (m, 1H). MS m/z: 379 (M+H+).
The HCl salt of the title compound was prepared as described in Example 418, except that 2-amino-5-(trifluoromethyl)benzonitrile was substituted for 6-amino-3-bromo-2-fluorobenzonitrile in step 2, acetic hydrazide for formic hydrazide in step 3, and 3-(N-tert-butoxycarbonyl-N-methylamino)azetidine for N-Boc-piperazine in step 5 of that route, as well as the Boc group was removed by HCl/THF without neutralization during the work-up. 1H NMR (300 MHz, CD3OD) δ: 8.55 (s, 1H), 7.94 (dd, J=8.7, 1.8 Hz, 1H), 7.81 (d, J=8.7 Hz, 1H), 5.03-4.93 (m, 2H), 4.85-4.67 (m, 2H), 4.30-4.22 (m, 1H), 2.82 (s, 3H), 2.62 (s, 3H). MS m/z: 337 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 122. 1H NMR (300 MHz, D2O) δ: 7.21 (s, 1H), 7.13 (s, 1H), 4.70-4.60 (m, 2H), 3.64 (d, J=11.1 Hz, 2H), 3.50-3.20 (m, 4H), 2.92 (s, 3H), 2.46 (s, 3H), 2.02 (s, 3H). MS m/z: 377 (M+H+).
The title compound was prepared analogously to Example 418. 1H NMR (300 MHz, CDCl3) δ: 8.72 (dd, J=7.2, 0.3 Hz, 1H), 7.32 (dd, J=9.3, 0.3 Hz, 1H), 4.14 (t, J=4.8 Hz, 4H), 2.63 (t, J=4.8 Hz, 4H), 2.61 (s, 3H), 2.38 (s, 3H). MS m/z: 427 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 111. 1H NMR (400 MHz, CD3OD) δ: 8.62 (s, 1H), 8.60 (s, 1H), 7.97 (d, J=8.8 Hz, 1H), 7.87 (d, J=8.8 Hz, 1H), 4.74 (dd, J=16.4, 3.2 Hz, 1H), 4.41-4.36 (m, 1H), 4.36-4.19 (m, 2H), 3.94-3.89 (m, 1H), 3.73-3.63 (m, 2H), 3.62-3.49 (m, 1H), 2.99 (s, 3H), 2.49-2.43 (m, 2H). MS m/z: 351 (M+H+).
The title compound was prepared analogously to Example 92. 1H NMR (400 MHz, DMSO-d6) δ: 8.65 (s, 1H), 8.41 (s, 1H), 7.92 (d, J=8.2 Hz, 1H), 7.69 (d, J=8.2 Hz, 1H), 4.23-4.19 (m, 4H), 3.01-2.98 (m, 2H), 2.79-2.75 (m, 2H), 2.36 (br, 1H), 1.91-1.87 (m, 2H). MS m/z: 337 (M+H+).
The title compound was prepared analogously to Example 111. 1H NMR (400 MHz, CDCl3) δ: 8.59 (s, 1H), 8.29 (s, 1H), 7.79 (dd, J=8.4, 1.6 Hz, 1H), 7.69 (d, J=8.4 Hz, 1H), 4.34-4.18 (m, 4H), 3.05 (br, 2H), 2.74-2.59 (m, 4H), 2.36 (s, 3H). MS m/z: 363 (M+H+).
The title compound was prepared analogously to Example 92. 1H NMR (400 MHz, CDCl3) δ: 8.60 (s, 1H), 8.29 (s, 1H), 7.80 (dd, J=8.8, 1.6 Hz, 1H), 7.70 (d, J=8.8 Hz, 1H), 4.36-4.14 (m, 4H), 3.22-3.19 (m, 2H), 3.01-2.92 (m, 4H). MS m/z: 349 (M+H+).
The title compound was prepared analogously to Example 36. 1H NMR (300 MHz, CDCl3) δ: 9.10 (s, 1H), 7.57 (dd, J=0.9 Hz, 1H), 7.32 (dd, J=1.1 Hz, 1H), 4.46-4.47 (m, 4H), 2.60-2.63 (m, 4H), 2.59 (s, 3H), 2.38 (s, 3H). MS m/z: 317 (M+H+).
The title compound was prepared as described in Example 34, except that 2-bromo-4-(trifluoromethyl)aniline was substituted for 4-fluoro-3-methylaniline as the starting material, tert-butyl piperazine-1-carboxylate for 1-methylpiperazine in step 7 of that route, and one extra step (step 10, described below) was included in that route. 1H NMR (300 MHz, DMSO-d6) δ: 10.13 (s, 1H), 8.49 (s, 1H), 7.67 (s, 1H), 4.38 (br, 4H), 2.56 (s, 3H), 2.53-2.48 (m, 4H), 2.46 (s, 3H). MS m/z: 351 (M+H+).
A 35 mL pressure tube was charged with tert-butyl 4-(6-bromo-8-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]quinoxalin-4-yl)piperazine-1-carboxylate (1.90 g, 3.8 mmol), trimethylboroxine (1.0 g, 8.3 mmol), Pd(dppf)Cl2 (310 mg, 0.38 mmol), K2CO3 (1.0 g, 7.8 mmol) and DMF (15 mL). After O2 was purged by bubbling N2 into the reaction solution, the tube was sealed and heated at 100° C. for 2 days. Work-up: the reaction mixture was poured into water (150 mL) and extracted with EtOAc (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 20% EtOAc in petroleum ether, to afford 1.2 g (72%) of the product as a yellow solid. 1H NMR (300 MHz, CDCl3) δ: 9.21 (s, 1H), 7.83 (s, 1H), 7.58 (s, 1H), 4.54-4.22 (br, 4H), 3.67-3.63 (m, 4H), 2.64 (s, 3H), 1.50 (s, 9H). MS m/z: 437 (M+H+).
The title compound was prepared analogously to Example 34. 1H NMR (300 MHz, DMSO-d6) δ: 10.00 (s, 1H), 8.06-8.00 (m, 1H), 7.41 (dd, J=17.4, 9.9 Hz, 1H), 4.38 (br, 4H), 2.53-2.49 (m, 4H), 2.24 (s, 3H). MS m/z: 305 (M+H+).
The title compound was prepared as described in Example 192, except that 2-amino-5-(trifluoromethyl)benzonitrile was substituted for 4-chloro-2-fluoroaniline in step 1 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.25 (s, 1H), 8.10 (d, J=1.4 Hz, 1H), 7.98 (d, J=1.4 Hz, 1H), 4.99 (br, 2H), 4.32 (br, 2H), 2.64 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 362 (M+H+).
The title compound was prepared analogously to Example 36. 1H NMR (300 MHz, DMSO-d6) δ: 9.67 (d, J=2.4 Hz, 1H), 7.55 (dd, J=18.6, 9.3 Hz, 1H), 7.43-7.38 (m, 1H), 4.32 (br, 4H), 2.50 (br, 4H), 2.24 (s, 3H). MS m/z: 305 (M+H+).
The HCl salt of the title compound was prepared as described in Example 192, except that 2-amino-5-(trifluoromethyl)benzonitrile was substituted for 4-chloro-2-fluoroaniline in step 1 of that route. 1H NMR (300 MHz, CDCl3) δ: 9.24 (s, 1H), 8.09 (s, 1H), 7.98 (s, 1H), 4.97 (br, 2H), 4.30 (br, 2H), 3.11 (t, J=5.1 Hz, 4H). MS m/z: 348 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 36. 1H NMR (300 MHz, DMSO-d6) δ: 10.04 (s, 1H), 8.28 (d, J=2.2 Hz, 1H), 7.45 (d, J=2.2 Hz, 1H), 4.53 (br, 4H), 3.29 (br, 4H), 2.53 (s, 3H). MS m/z: 303 (M+H+).
The HCl salt of the title compound was prepared as described in Example 464 step 11. 1H NMR (300 MHz, DMSO-d6) δ: 10.20 (s, 1H), 9.54 (br, 2H), 8.56 (s, 1H), 7.72 (s, 1H), 6.01-5.93 (br, 4H), 4.62-4.58 (br, 4H), 2.60 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Example 1 steps 1-3.
A 100 mL round bottom flask was charged with 2,6-dichloro-3-hydrazinylquinoxaline (1.2 g, 5.2 mmol), triethylamine (0.77 g, 7.8 mmol) and THF (30 mL). To the mixture was added dropwise 2-(thiophen-2-yl)acetyl chloride (0.92 g, 5.7 mmol) at 0° C. The resulting solution was stirred at room temperature for 15 minutes. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:1). Work-up: the reaction mixture was diluted with EtOAc (80 mL). The organic solution was washed with brine (60 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 20% EtOAc in petroleum ether, to afford 1.2 g (65%) of the product.
A 100 mL round bottom flask was charged with POCl3 (30 mL). To the above was added N′-(3,7-dichloroquinoxalin-2-yl)-2-(thiophen-2-yl)acetohydrazide (1.2 g, 3.4 mmol). The resulting mixture was heated at 120° C. for 30 minutes. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:3). Work-up: the reaction mixture was concentrated in vacuo. The residue was poured into ice-water and extracted with EtOAc. The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 15% EtOAc in petroleum ether, to afford 1.0 g (80%) of the product.
A 100 mL round bottom flask was charged with 4,8-dichloro-1-(thiophen-2-ylmethyl)-[1,2,4]triazolo[4,3-a]quinoxaline (0.2 g, 0.6 mmol), 1-methylpiperazine (0.18 g, 1.8 mmol) and THF (60 mL). The resulting solution was stirred at room temperature for 1 h. Reaction progress was monitored by TLC (methanol/dichloromethane=1:20). Work-up: the reaction mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 10% MeOH in dichloromethane, to afford 0.21 g (85%) of the product. 1H NMR (300 MHz, CDCl3) δ: 7.85 (d, J=2.1 Hz, 1H), 7.56 (d, J=8.8 Hz, 1H), 7.33 (dd, J=8.8, 2.1 Hz, 1H), 7.23 (dd, J=5.1, 1.2 Hz, 1H), 6.94 (dd, J=5.1, 3.6 Hz, 1H), 6.84 (dd, J=3.6, 1.2 Hz, 1H), 4.98 (s, 2H), 4.46 (br, 4H), 2.63 (t, J=5.1 Hz, 4H), 2.39 (s, 3H). MS m/z: 399 (M+H+).
The title compound was prepared as described in Example 471, except that 2-(thiophen-3-yl)acetyl chloride was substituted for 2-(thiophen-2-yl)acetyl chloride in step 4 of that route. 1H NMR (300 MHz, CDCl3) δ: 7.80 (d, J=2.1 Hz, 1H), 7.54 (d, J=8.7 Hz, 1H), 7.36-7.31 (m, 2H), 7.05-6.95 (m, 2H), 4.80 (s, 2H), 4.46 (br, 4H), 2.62 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 399 (M+H+).
The title compound was prepared as described in Example KLP-471, except that piperazine was substituted for 1-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, CDCl3) δ: 7.85 (d, J=2.4 Hz, 1H), 7.55 (d, J=8.8 Hz, 1H), 7.33 (dd, J=8.8, 2.4 Hz, 1H), 7.23 (dd, J=5.1, 1.2 Hz, 1H), 6.94 (dd, J=5.1, 3.6, 1H), 6.85 (dd, J=3.6, 1.2 Hz, 1H), 4.98 (s, 2H), 4.44 (br, 4H), 3.10 (t, J=5.1 Hz, 4H). MS m/z: 385 (M+H+).
The title compound was prepared as described in Example 471, except that 2-(thiophen-3-yl)acetyl chloride was substituted for 2-(thiophen-2-yl)acetyl chloride in step 4, piperazine for 1-methylpiperazine in step 6 of that route. 1H NMR (300 MHz, CDCl3) δ: 7.80 (d, J=2.4 Hz, 1H), 7.54 (d, J=8.7 Hz, 1H), 7.35-7.30 (m, 2H), 7.05-6.95 (m, 2H), 4.81 (s, 2H), 4.42 (br, 4H), 3.08 (t, J=5.1 Hz, 4H). MS m/z: 385 (M+H+).
The title compound was prepared analogously to Example 243. 1H NMR (300 MHz, CD3OD) δ: 8.51 (s, 1H), 8.02 (t, J=2.1 Hz, 1H), 7.37 (dd, J=10.2, 2.4 Hz, 1H), 4.42 (br, 4H), 2.64 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 321 (M+H+).
The title compound was prepared analogously to Example 241. 1H NMR (300 MHz, CDCl3) δ: 8.45 (dd, J=1.8, 0.6 Hz, 1H), 7.69 (dd, J=8.7, 0.6 Hz, 1H), 7.64 (dd, J=8.7, 1.8 Hz, 1H), 4.48 (br, 4H), 2.65 (s, 3H), 2.61 (t, J=5.1 Hz, 4H), 2.37 (s, 3H). MS m/z: 308 (M+H+).
The title compound was prepared analogously to Example 243. 1H NMR (300 MHz, DMSO-d6) δ: 8.72 (s, 1H), 7.94 (t, J=2.0 Hz, 1H), 7.59 (dd, J=10.8, 2.0 Hz, 1H), 4.18 (br, 4H), 2.87-2.81 (m, 4H). MS m/z: 307 (M+H+).
The title compound was prepared analogously to Example 243. 1H NMR (300 MHz, CDCl3) δ: 8.39-8.37 (m, 2H), 7.58 (s, 2H), 5.67-5.56 (m, 2H), 3.36-3.14 (m, 3H), 2.99-2.90 (m, 1H), 2.42-2.34 (m, 1H), 2.24-2.02 (m, 2H), 2.01-1.70 (m, 3H), 1.60-1.52 (m, 1H). MS m/z: 373 (M+H+).
The HCl salt of the title compound was prepared as described in Example 181, except that 4-bromobenzene-1,2-diamine was substituted for 4-chlorobenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 8.44 (d, J=1.6 Hz, 1H), 8.28-8.26 (m, 1H), 7.65 (d, J=1.6 Hz, 1H), 7.59-7.58 (m, 2H), 4.50 (t, J=5.4 Hz, 4H), 3.33-3.31 (m, 4H). MS m/z: 332 (M+H+).
The HCl salt of the title compound was prepared as described in Example 181, except that 4-bromobenzene-1,2-diamine was substituted for 4-chlorobenzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CD3OD) δ: 8.69 (d, J=1.5 Hz, 1H), 8.47 (d, J=2.1 Hz, 1H), 7.88 (d, J=1.5 Hz, 1H), 7.81 (d, J=9.0 Hz, 1H), 7.73 (dd, J=9.0, 2.1 Hz, 1H), 5.57-5.51 (m, 2H), 3.82-3.73 (m, 4H), 3.46-3.42 (m, 2H), 3.00 (s, 1H). MS m/z: 346 (M+H+).
The title compound was prepared analogously to Example 180. 1H NMR (300 MHz, CDCl3) δ: 7.96-7.94 (m, 2H), 7.69-7.60 (m, 3H), 4.54 (br, 4H), 2.60 (t, J=5.1 Hz, 4H), 2.36 (s, 3H). MS m/z: 293 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 180. 1H NMR (300 MHz, CD3OD) δ: 8.60 (d, J=2.7 Hz, 1H), 8.41 (d, J=6.9 Hz, 1H), 7.83 (d, J=2.7 Hz, 1H), 7.67 (d, J=9.9 Hz, 1H), 5.59 (d, J=14.4 Hz, 2H), 3.80-3.68 (m, 4H), 3.34-3.26 (m, 4H), 1.42 (t, J=7.5 Hz, 3H). MS m/z: 334 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 9. 1H NMR (300 MHz, DMSO-d6) δ: 10.56 (s, 1H), 8.53 (s, 1H), 8.43 (s, 1H), 7.59-7.56 (m, 2H), 5.60-5.51 (m, 2H), 3.59-3.49 (m, 4H), 3.25-3.11 (m, 2H), 2.79 (s, 3H), 2.40 (s, 3H). MS m/z: 360 (M+H+).
The HCl salt of the title compound was prepared as described in Example 180, except that 4-bromobenzene-1,2-diamine was substituted for 4-chlorobenzene-1,2-diamine as the starting material, and the other regio-isomer in the reaction with 2-aminoethanol was isolated, of that route. 1H NMR (300 MHz, CD3OD) δ: 8.61 (d, J=1.4 Hz, 1H), 8.07 (d, J=8.7 Hz, 1H), 8.02 (d, J=2.1 Hz, 1H), 7.84 (d, J=1.4 Hz, 1H), 7.65 (dd, J=8.7, 2.1 Hz, 1H), 5.62-5.56 (m, 2H), 3.75-3.66 (m, 4H), 3.43-3.37 (m, 2H), 3.00 (s, 3H). MS m/z: 346 (M+H+).
The HCl salt of the title compound was prepared as described in Example 180, except that 4-bromobenzene-1,2-diamine was substituted for 4-chlorobenzene-1,2-diamine as the starting material, and the other regio-isomer in the reaction with 2-aminoethanol was isolated, of that route. 1H NMR (300 MHz, CD3OD) δ: 8.50 (d, J=1.4 Hz, 1H), 7.99 (d, J=8.4 Hz, 1H), 7.93 (d, J=2.1 Hz, 1H), 7.74 (d, J=1.4 Hz, 1H), 7.57 (dd, J=8.4, 2.1 Hz, 1H), 4.62 (t, J=5.4 Hz, 4H), 3.46 (t, J=5.4 Hz, 4H). MS m/z: 332 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 11. 1H NMR (400 MHz, DMSO-d6) δ: 10.94 (br, 1H), 8.48 (s, 1H), 8.08 (d, J=8.8 Hz, 1H), 7.79 (d, J=2.0 Hz, 1H), 7.54 (dd, J=8.8, 2.0 Hz, 1H), 5.60 (d, J=13.6 Hz, 2H), 3.62-3.55 (m, 4H), 3.20-3.15 (m, 2H), 2.79 (d, J=4.4 Hz, 3H), 2.41 (s, 3H). MS m/z: 346 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 9. 1H NMR (300 MHz, DMSO-d6) δ: 9.56 (br, 1H), 8.53 (s, 1H), 8.43-8.42 (m, 1H), 7.58-7.57 (m, 2H), 4.54 (br, 4H), 3.26 (br, 4H), 2.40 (s, 3H). MS m/z: 346 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 11. 1H NMR (400 MHz, DMSO-d6) δ: 9.23 (br, 1H), 8.47 (s, 1H), 8.07 (d, J=8.8 Hz, 1H), 7.77 (d, J=1.8 Hz, 1H), 7.53 (dd, J=8.8, 1.8 Hz, 1H), 4.54 (br, 4H), 3.28 (br, 4H), 2.40 (s, 3H). MS m/z: 360 (M+H+).
The title compound was prepared as described in Example 12, except that 2-amino-5-iodobenzoic acid was substituted for 2-amino-5-chlorobenzoic acid as the starting material and N-methylpiperazine for piperazine (Reference for introducing cyano group in step 2: D M Tschaen et al, Synth. Commun. 1994, 24(6), 887-890). The compound exists as a mixture of cyclic tetrazolo structure and linear azido structure. 1H NMR (300 MHz, CD3OD) δ: 8.76 (d, J=1.8 Hz, 0.33H), 8.16 (d, J=1.8 Hz, 0.67H), 8.02 (dd, J=8.7, 1.8 Hz, 0.33H), 7.80 (dd+d, J=8.7, 1.8 Hz, 0.67H+0.33H), 7.51 (d, J=8.7 Hz, 0.67H), 4.33 (t, J=5.1 Hz, 1.33H), 4.04 (t, J=5.1 Hz, 2.67H), 2.76 (t, J=5.1 Hz, 1.33H), 2.69 (t, J=5.1 Hz, 2.67H), 2.46 (s, 2.00H), 2.43 (s, 1.00H). 1H NMR (300 MHz, CDCl3) δ: 8.79 (d, J=1.8 Hz, 0.2H), 8.12 (d, J=1.8 Hz, 0.8H), 7.90 (dd, J=8.8, 1.8 Hz, 0.2H), 7.77 (d, J=8.8 Hz, 0.2H), 7.70 (dd, J=8.8, 1.8 Hz, 0.8H), 7.47 (d, J=8.8 Hz, 0.8H), 4.36 (t, J=5.1 Hz, 0.8H), 4.00 (t, J=5.1 Hz, 3.2H), 2.67 (t, J=5.1 Hz, 0.8H), 2.50 (t, J=5.1 Hz, 3.2H), 2.40 (s, 0.6H), 2.36 (s, 2.4H). MS m/z: 295 (M+H+).
The title compound was prepared analogously to Example 201. 1H NMR (300 MHz, CDCl3) δ: 8.24 (d, J=2.4 Hz, 1H), 7.45 (d, J=2.4 Hz, 1H), 4.42 (br, 4H), 2.65-2.62 (m, 4H), 2.61 (s, 3H), 2.39 (s, 3H). MS m/z: 318 (M+H+).
The title compound was prepared as described in Example 27, except that 3,4-diamino-5-fluorobenzonitrile (prepared as described in Example 196 steps 1-2, except that 4-amino-3-fluorobenzonitrile was substituted for 4-chloro-2-fluoroaniline) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CDCl3) δ: 8.47 (t, J=1.6 Hz, 1H), 7.56 (dd, J=9.4, 1.6 Hz, 1H), 4.83 (br, 2H), 4.26 (br, 2H), 2.66-2.62 (m, 4H), 2.39 (s, 3H). MS m/z: 313 (M+H+).
The title compound was prepared analogously to Example 187. 1H NMR (300 MHz, DMSO-d6) δ: 8.17-8.11 (m, 1H), 7.57-7.47 (m, 1H), 4.33 (br, 4H), 2.56-2.48 (m, 4H), 2.26 (s, 3H). MS m/z: 306 (M+H+).
The title compound was prepared as described in Example 27, except that 2,3-diamino-5-(trifluoromethyl)benzonitrile (prepared as described in Example 196 steps 1-2, except that 2-amino-5-(trifluoromethyl)benzonitrile was substituted for 4-chloro-2-fluoroaniline) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material of that route. 1H NMR (300 MHz, CDCl3) δ: 8.78 (s, 1H), 8.11 (s, 1H), 4.89 (br, 2H), 4.35 (br, 2H), 2.68-2.64 (m, 4H), 2.39 (s, 3H). MS m/z: 363 (M+H+).
The title compound was prepared as described in Example 187, except that 2-bromo-4-(trifluoromethyl)aniline was substituted for 4-fluoro-3-(trifluoromethyl)aniline as the starting material of that route, and one extra step (step 9, as described in Example 464 step 10, except that tert-butyl 4-(6-bromo-8-(trifluoromethyl)tetrazolo[1,5-a]quinoxalin-4-yl)piperazine-1-carboxylate was substituted for tert-butyl 4-(6-bromo-8-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]quinoxalin-4-yl)piperazine-1-carboxylate) was included in that route. 1H NMR (300 MHz, CDCl3) δ: 8.51 (s, 1H), 7.68 (s, 1H), 4.53-4.48 (br, 4H), 2.68 (s, 3H), 2.64 (t, J=5.4 Hz, 4H), 2.39 (s, 3H). MS m/z: 352 (M+H+).
The title compound was prepared analogously to Example 201. 1H NMR (300 MHz, DMSO-d6) δ: 7.81-7.71 (m, 1H), 7.61-7.55 (m, 1H), 4.28 (br, 4H), 2.55-2.48 (m, 4H), 2.26 (s, 3H). MS m/z: 306 (M+H+).
The HCl salt of the title compound was prepared as described in Example 27, except that 3,4-diamino-5-fluorobenzonitrile (prepared as described in Example 196 steps 1-2, except that 4-amino-3-fluorobenzonitrile was substituted for 4-chloro-2-fluoroaniline) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material, and tert-butyl piperazine-1-carboxylate for 1-methylpiperazine of that route. 1H NMR (300 MHz, CD3OD/DMSO-d6) δ: 7.96 (s, 1H), 7.20 (d, J=7.5 Hz, 1H), 4.00 (br, 4H), 2.75-2.70 (m, 4H). MS m/z: 299 (M+H+).
The title compound was prepared as described in Example 27, except that 3,4-diamino-5-fluorobenzonitrile (prepared as described in Example 196 steps 1-2, except that 4-amino-3-fluorobenzonitrile was substituted for 4-chloro-2-fluoroaniline) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material, and octahydropyrrolo[1,2-a]pyrazine for 1-methylpiperazine of that route. 1H NMR (300 MHz, CDCl3) δ: 8.48 (t, J=1.5 Hz, 1H), 7.56 (dd, J=9.6, 1.5 Hz, 1H), 6.22-6.08 (m, 1H), 5.46-5.30 (m, 1H), 3.66-2.35 (m, 5H), 2.27-1.79 (m, 6H). MS m/z: 339 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 201. 1H NMR (300 MHz, DMSO-d6) δ: 8.26 (s, 1H), 7.70 (s, 1H), 4.49 (br, 4H), 3.33 (br, 4H), 2.60 (s, 3H). MS m/z: 304 (M+H+).
The HCl salt of the title compound was prepared as described in Example 27, except that 2,3-diamino-5-(trifluoromethyl)benzonitrile (prepared as described in Example 196 steps 1-2, except that 2-amino-5-(trifluoromethyl)benzonitrile was substituted for 4-chloro-2-fluoroaniline) was substituted for 4-(trifluoromethyl)benzene-1,2-diamine as the starting material, and tert-butyl piperazine-1-carboxylate for 1-methylpiperazine of that route. 1H NMR (300 MHz, DMSO-d6) δ: 9.73 (br, 2H), 8.90 (s, 1H), 8.67 (s, 1H), 4.92 (br, 2H), 4.42 (br, 2H), 3.37 (br, 4H). MS m/z: 349 (M+H+).
The HCl salt of the title compound was prepared as described in Example 494 step 10. 1H NMR (300 MHz, DMSO-d6) δ: 9.41-9.39 (br, 2H), 8.48 (s, 1H), 7.96 (s, 1H), 4.61-4.54 (br, 4H), 3.42-3.31 (br, 4H), 2.68 (s, 3H). MS m/z: 338 (M+H+).
A 250 mL round bottom flask was charged with fuming HNO3 (17 mL) and concentrated H2SO4 (2.5 mL) at −20° C. To the above was added in portions 1-(3-chlorophenyl)ethanone (5.0 g, 32.3 mmol) over 15 minutes. The mixture was allowed to warm to −10° C. and stirred for 5 h at this temperature, after which ice-water (75 mL) was added and the reaction mixture was extracted with dichloromethane (50 mL×2). The combined organic layers were washed with brine (30 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 2% EtOAc in petroleum ether, to afford 5.0 g (78%) of the product as an off-white crystal.
A 100 mL round bottom flask was charged with 1-(5-chloro-2-nitrophenyl)ethanone (4.00 g, 20.2 mmol), N,N-dimethylformamide dimethyl acetal (2.65 g, 22.3 mmol) and DMF (25 mL). The mixture was heated at 100° C. for 2 h under N2. It was then concentrated under reduced pressure to dryness. The residue was mixed with ethyl ether (20 mL). The solid was collected by filtration, washed with more ethyl ether (10 mL×2), and dried to afford 3.15 g (62%) of the product as a yellow solid.
A 100 mL round bottom flask was charged with 1-(5-chloro-2-nitrophenyl)-3-(dimethylamino)prop-2-en-1-one (3.15 g, 12.5 mmol), hydrazine hydrate (0.69 g, 13.8 mmol) and ethanol (32 mL). The mixture was stirred at 90° C. for 9.5 h under N2. It was then concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 2.3 g (83%) of the product as an off-white crystal.
A 100 mL round bottom flask was charged with 5-(5-chloro-2-nitrophenyl)-1H-pyrazole (2.3 g, 10.4 mmol), Na2S2O4 (5.4 g, 31.0 mmol), methanol (23 mL) and water (10 mL). The mixture was heated at reflux for 0.5 h under N2. It was then concentrated in vacuo. The residue was basified with saturated aqueous NaHCO3 (20 mL) to pH 9 and extracted with EtOAc (30 mL×2). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 0.76 g (38%) of the product as a yellow crystal.
A 100 mL round bottom flask was charged with 4-chloro-2-(1H-pyrazol-5-yl)aniline (0.76 g, 3.9 mmol), K2CO3 (0.81 g, 5.9 mmol) and THF (40 mL). To the above was added in portions triphosgene (1.39 g, 4.7 mmol). The mixture was heated at reflux for 4 h under N2. It was then concentrated under reduced pressure to dryness. The solid residue was washed with water (20 mL) and dichloromethane (20 mL×2) and dried, to afford 0.63 g (74%) of the product as an off-white solid.
A 50 mL round bottom flask was charged with 9-chloropyrazolo[1,5-c]quinazolin-5(6H)-one (0.41 g, 1.87 mmol), phosphorus oxychloride (10 mL) and diisopropylethylamine (2 mL). The resulting mixture was heated at reflux for 3 h under N2. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:5). Work-up: the mixture was concentrated in vacuo. The residue was cautiously poured into ice water, neutralized with saturated aqueous NaHCO3 (20 mL) and extracted with EtOAc (20 mL×3). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 0.30 g (68%) of the product as a white solid.
A 50 mL round bottom flask was charged with 5,9-dichloropyrazolo[1,5-c]quinazoline (0.30 g, 1.27 mmol), 1-methylpiperazine (0.14 g, 1.40 mmol), triethylamine (0.38 g, 3.81 mmol) and THF (10 mL). The mixture was heated at 60° C. for 0.5 h under N2. It was then concentrated in vacuo. The residue was mixed with water (20 mL) and extracted with dichloromethane (20 mL×3). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 0.38 g (99%) of the product as an off-white solid. To the solution of the product in EtOAc (20 mL) was added a solution (2 mL) of HCl in EtOAc with stifling. The precipitate was collected by filtration, washed with ethyl ether (10 mL×2) and dried, to afford 0.39 g (92%) of the corresponding HCl salt as an off-white solid. 1H NMR (300 MHz, D2O) δ: 7.97 (d, J=2.1 Hz, 1H), 7.47 (s, 1H), 7.30-7.10 (m, 2H), 6.76 (s, 1H), 4.60-4.40 (m, 2H), 3.75-3.55 (m, 2H), 3.45-3.25 (m, 4H), 2.96 (s, 3H). MS m/z: 302 (M+H+).
A 1 L round bottom flask was charged with 4-(trifluoromethyl)aniline (50.0 g, 0.31 mol), IC1 (60.0 g, 0.37 mol), methanol (100 mL) and dichloromethane (300 mL). The resulting mixture was stirred for 1 h at room temperature. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:20). Work-up: the reaction solution was diluted with saturated Na2SO3 (500 mL) and then extracted with CH2Cl2 (600 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with petroleum ether, to afford 60.0 g (67%) of the product as a light-red oil. MS m/z: 288 (M+H+).
A 1 L round bottom flask was charged with 2-iodo-4-(trifluoromethyl)aniline (60 g, 0.21 mol) and triethylamine (300 mL). To the above solution was added trimethylsilylacetylene (88 mL, 0.62 mol), followed by the addition of PdCl2(PPh3)2 (4.4 g, 6.3 mmol) and cuprous iodide (1.6 g, 8.4 mmol). The resulting mixture was stirred for 1 h at room temperature under N2 atmosphere. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:20). Work-up: the reaction solution was diluted with saturated aqueous NaHCO3 (300 mL) and then extracted with EtOAc (400 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with petroleum ether, to afford 50.0 g (93%) of the product as a light-red oil. MS m/z: 258 (M+H+).
A 1 L round bottom flask was charged with 4-(trifluoromethyl)-2-((trimethylsilyl)ethynyl)aniline (50.0 g, 0.19 mol) and methanol (300 mL). To the above solution was added K2CO3 (29 g, 0.21 mol). The resulting mixture was stirred for 0.5 h at room temperature. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:20). Work-up: the reaction solution was diluted with saturated aqueous NaHCO3 (300 mL) and then extracted with EtOAc (400 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with petroleum ether, to afford 30.0 g (83%) of the product as a light-red oil. MS m/z: 186 (M+H+).
A 300 mL pressure vessel was charged with 2-ethynyl-4-(trifluoromethyl)aniline (12.0 g, 65 mmol), CuI (0.35 g, 1.8 mmol), azidotrimethylsilane (8.2 g, 71 mmol), methanol (8 mL) and DMF (72 mL). The vessel was sealed and the reaction mixture was magnetically stirred at 100° C. for 12 h. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:10). Work-up: the reaction solution was diluted with saturated aqueous NaHCO3 (100 mL) and then extracted with EtOAc (150 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with petroleum ether, to afford 9.0 g (61%) of the product as a light-red oil. MS m/z: 229 (M+H+).
A 1 L round bottom flask was charged with 2-(1H-1,2,3-triazol-5-yl)-4-(trifluoromethyl)aniline (20.0 g, 88 mmol) and THF (300 mL). To the above solution were added K2CO3 (18.2 g, 0.13 mol) and thiophosgene (15.1 g, 0.13 mol). The resulting mixture was stirred for 10 h at reflux. Reaction progress was monitored by TLC (EtOAc/petroleum ether=3:1). Work-up: the reaction solution was concentrated in vacuo. The resulting crystalline solid was collected by filtration, washed with water (50 mL) and ethyl ether (100 mL), and dried to afford 16.0 g (68%) of the product as a red solid. MS m/z: 271 (M+H+).
A 1 L round bottom flask was charged with 9-(trifluoromethyl)-[1,2,3]triazolo[1,5-c]quinazoline-5(6H)-thione (16.0 g, 59 mmol), 1-methylpiperazine (11.9 g, 0.12 mol) and 1,4-dioxane (500 mL). To the above solution was added 30% aqueous H2O2 (5 mL) at 0° C. The resulting mixture was stirred for 0.5 h at that temperature. Reaction progress was monitored by TLC (EtOAc/petroleum ether=3:1). Work-up: the reaction solution was diluted with saturated aqueous Na2SO3 (200 mL) and then extracted with CH2Cl2 (300 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 4% MeOH in CH2Cl2, to afford 8.0 g (40%) of the product as a light-orange solid. 1H NMR (300 MHz, CDCl3) δ: 8.39 (s, 1H), 8.19 (s, 1H), 7.78 (s, 2H), 4.28 (t, J=4.8 Hz, 4H), 2.68 (t, J=4.8 Hz, 4H), 2.40 (s, 3H). MS m/z: 337 (M+H+).
The title compound was prepared as described in Example 502, except that 4-bromo-3-fluoroaniline was substituted for 4-(trifluoromethyl)aniline in step 1 of that route. 1H NMR (300 MHz, CDCl3) δ: 8.27 (s, 1H), 8.12 (d, J=7.2 Hz, 1H), 7.42 (d, J=9.6 Hz, 1H), 4.22 (t, J=4.8 Hz, 4H), 2.67 (t, J=4.8 Hz, 4H), 2.39 (s, 3H). MS m/z: 365 (M+H+).
The title compound was prepared analogously to Example 502. 1H NMR (300 MHz, CDCl3) δ: 8.32 (s, 1H), 7.92 (dd, J=2.4, 0.3 Hz, 1H), 7.65 (dd, J=8.7, 0.3 Hz, 1H), 7.54 (dd, J=8.7, 2.4 Hz, 1H), 4.17 (t, J=5.1 Hz, 4H), 2.68 (t, J=5.1 Hz, 4H), 2.40 (s, 3H). MS m/z: 303 (M+H+).
The title compound was prepared analogously to Example 502. 1H NMR (400 MHz, CDCl3) δ: 8.38 (s, 1H), 8.25 (s, 1H), 7.78 (d, J=8.8 Hz, 1H), 7.72 (d, J=8.8 Hz, 1H), 4.33 (br, 4H), 2.68 (br, 4H), 2.40 (s, 3H). MS m/z: 294 (M+H+).
The title compound was prepared analogously to Example 501. 1H NMR (300 MHz, CDCl3) δ: 8.03 (d, J=1.8 Hz, 1H), 7.99 (d, J=2.1 Hz, 1H), 7.59 (dd, J=8.7, 2.1 Hz, 1H), 7.54 (d, J=8.7 Hz, 1H), 6.90 (d, J=1.8 Hz, 1H), 4.04 (br, 4H), 2.67 (t, J=5.1 Hz, 4H), 2.39 (s, 3H). MS m/z: 346 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 501. 1H NMR (300 MHz, D2O) δ: 7.90 (d, J=2.1 Hz, 1H), 7.41 (d, J=2.1 Hz, 1H), 7.22 (dd, J=8.7, 2.1 Hz, 1H), 6.98 (d, J=8.7 Hz, 1H), 6.62 (d, J=2.1 Hz, 1H), 3.84 (br, 4H), 3.48-3.42 (m, 4H). MS m/z: 332 (M+H+).
The HCl salt of the title compound was prepared as described in Example 501, except that 1-(3-bromo-4-fluorophenyl)ethanone was substituted for 1-(3-chlorophenyl)ethanone in step 1, and N,N-dimethylformamide di-tert-butyl acetal for N,N-dimethylformamide dimethyl acetal in step 2 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 11.16 (s, 1H), 8.66 (d, J=7.5 Hz, 1H), 8.23 (d, J=1.8 Hz, 1H), 8.56 (d, J=9.9 Hz, 1H), 7.43 (d, J=1.8 Hz, 1H), 4.97 (d, J=14.1 Hz, 2H), 3.65-3.55 (m, 4H), 3.33-3.25 (m, 2H), 2.81 (d, J=4.8 Hz, 3H). MS m/z: 364 (M+H+).
The title compound was prepared analogously to Example 501. 1H NMR (300 MHz, CDCl3) δ: 8.14 (d, J=1.5 Hz, 1H), 7.68 (dd, J=8.7, 1.5 Hz, 1H), 7.63 (d, J=8.7 Hz, 1H), 6.75 (s, 1H), 4.23 (br, 4H), 2.74 (br, 4H), 2.52 (s, 3H), 2.44 (s, 3H). MS m/z: 307 (M+H+).
The HCl salt of the title compound was prepared as described in Example 501, except that 1-(3-bromo-4-fluorophenyl)ethanone was substituted for 1-(3-chlorophenyl)ethanone in step 1, N,N-dimethylformamide di-tert-butyl acetal for N,N-dimethylformamide dimethyl acetal in step 2, and piperazine for 1-methylpiperazine in step 7 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.62 (d, J=7.8 Hz, 1H), 8.21 (d, J=2.4 Hz, 1H), 7.55 (d, J=10.2 Hz, 1H), 7.39 (d, J=2.4 Hz, 1H), 4.20 (t, J=5.1 Hz, 4H), 3.32 (t, J=5.1 Hz, 4H). MS m/z: 350 (M+H+).
The title compound was prepared as described in Example 501, except that 1-(3-bromophenyl)ethanone was substituted for 1-(3-chlorophenyl)ethanone in step 1, and N,N-dimethylacetamide dimethyl acetal for N,N-dimethylformamide dimethyl acetal in step 2 of that route. 1H NMR (300 MHz, CDCl3) δ: 7.96 (d, J=2.1 Hz, 1H), 7.57 (dd, J=7.8, 2.1 Hz, 1H), 7.52 (d, J=7.8 Hz, 1H), 6.68 (s, 1H), 4.02 (br, 4H), 2.66 (t, J=5.1 Hz, 4H), 2.51 (s, 3H), 2.38 (s, 3H). MS m/z: 360 (M+H+).
The title compound was prepared analogously to Example 501, except that N,N-dimethylacetamide dimethyl acetal was substituted for N,N-dimethylformamide dimethyl acetal in step 2 of that route. 1H NMR (300 MHz, DMSO-d6) δ: 8.19 (dd, J=2.1, 1.2 Hz, 1H), 7.57-7.50 (m, 2H), 7.16 (s, 1H), 3.92 (t, J=4.8 Hz, 4H), 2.53-2.48 (m, 4H), 2.44 (s, 3H), 2.24 (s, 3H). MS m/z: 316 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 501. 1H NMR (300 MHz, D2O) δ: 7.86 (s, 1H), 7.53 (d, J=8.7 Hz, 1H), 7.38 (d, J=8.7 Hz, 1H), 6.59 (s, 1H), 4.60-4.55 (m, 2H), 3.62-3.57 (m, 2H), 3.36-3.28 (m, 4H), 2.90 (s, 3H), 2.33 (s, 3H). MS m/z: 350 (M+H+).
A 50 mL round bottom flask was charged with 4-chloro-2-fluoro-1-nitrobenzene (2.0 g, 11.4 mmol), dimethyl 1H-imidazole-4,5-dicarboxylate (2.3 g, 12.5 mmol), Cs2CO3 (4.5 g, 13.7 mmol) and DMF (30 mL). The mixture was heated at 80° C. for 12 h then cooled to room temperature and diluted with water (100 mL). The mixture was extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine (50 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 1% methanol in dichloromethane, to afford 3.1 g (81%) of the product as a yellow crystal.
A 50 mL round bottom flask was charged with dimethyl 1-(5-chloro-2-nitrophenyl)-1H-imidazole-4,5-dicarboxylate (1.5 g, 4.40 mmol), iron powder (0.99 g, 17.2 mmol) and acetic acid (15 mL). The mixture was heated at 100° C. for 12 h and then concentrated under reduced pressure to dryness. 1 M HCl (50 mL) was then added slowly to remove any unreacted iron. The solid remained was collected by filtration and dried to afford 2.2 g of the product as a gray solid, which was used in the next step without further purification.
A 100 mL round bottom flask was charged with methyl 8-chloro-4-oxo-4,5-dihydroimidazo[1,5-a]quinoxaline-3-carboxylate (2.2 g crude from last step, 4.40 mmol), LiOH (0.92 g, 22.0 mmol), THF (30 mL) and water (30 mL). The mixture was stirred at 25° C. for 12 h and then concentrated in vacuo. The solid was collected by filtration and dried, to afford 1.0 g (86% for 2 steps) of the product as an off-white solid.
A 50 mL round bottom flask was charged with 8-chloro-4-oxo-4,5-dihydroimidazo[1,5-a]quinoxaline-3-carboxylic acid (0.60 g, 2.27 mmol) and diphenyl ether (20 mL). The mixture was heated at 250° C. for 2.5 h under N2 then cooled to room temperature. It was diluted with petroleum ether (50 mL). The solid was collected by filtration and dried, to afford 0.41 g (82%) of the product as a gray solid.
A 50 mL round bottom flask was charged with 8-chloroimidazo[1,5-a]quinoxalin-4(5H)-one (0.41 g, 1.86 mmol), phosphorus oxychloride (10 mL) and diisopropylethylamine (2 mL). The resulting mixture was stirred at reflux overnight. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:2). Work-up: the mixture was concentrated in vacuo. The residue was cautiously poured into ice water, neutralized with saturated aqueous NaHCO3 (50 mL) and extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine (30 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 0.60 g of the product as a yellow solid.
A 50 mL round bottom flask was charged with 4,8-dichloroimidazo[1,5-a]quinoxaline (0.60 g, 2.52 mmol), 1-methylpiperazine (0.76 g, 7.55 mmol) and THF (15 mL). The mixture was heated at 60° C. for 12 h and then cooled to room temperature. It was diluted with water (20 mL) and extracted with EtOAc (20 mL×3). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 2% methanol in dichloromethane, to afford 0.16 g (29% for 2 steps) of the free base of the product as an off-white solid. To its solution in THF (15 mL) was added slowly a solution (2 mL) of HCl in EtOAc with stirring. The precipitate was collected by filtration, washed with ethyl ether (10 mL×2), and dried, to afford 0.12 g of the corresponding HCl salt as an off-white solid. 1H NMR (300 MHz, D2O) δ: 9.42 (s, 1H), 8.23 (s, 1H), 8.00 (s, 1H), 7.51 (d, J=8.7 Hz, 1H), 7.43 (d, J=8.7 Hz, 1H), 4.60-4.40 (m, 2H), 3.75-3.50 (m, 4H), 3.40-3.20 (m, 2H), 2.90 (s, 3H). MS m/z: 302 (M+H+).
A 50 mL round bottom flask was charged with 4-chloro-2-fluoro-1-nitrobenzene (2.0 g, 11.4 mmol), methyl 1H-pyrrole-2-carboxylate (1.4 g, 11.4 mmol), Cs2CO3 (4.5 g, 13.7 mmol) and DMF (35 mL). The mixture was heated at 60° C. for 24 h and then cooled to room temperature. It was diluted with water (100 mL) and extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine (50 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 1% EtOAc in petroleum ether, to afford 2.8 g (88%) of the product as a yellow crystal.
A 50 mL round bottom flask was charged with methyl 1-(5-chloro-2-nitrophenyl)-1H-pyrrole-2-carboxylate (1.2 g, 4.30 mmol), iron powder (0.96 g, 17.2 mmol) and AcOH (12 mL). The mixture was heated at 100° C. for 12 h and then concentrated under reduced pressure to dryness. 1 M HCl (50 mL) was then added slowly to remove any unreacted iron. The solid remained was collected by filtration and dried to afford 0.86 g (92%) of the product as a gray solid.
A 50 mL round bottom flask was charged with 8-chloropyrrolo[1,2-a]quinoxalin-4(5H)-one (0.86 g, 3.94 mmol), phosphorus oxychloride (10 mL) and diisopropylethylamine (2 mL). The resulting mixture was heated at reflux for 1 h under N2. Reaction progress was monitored by TLC (EtOAc/Petroleum ether=1:20). Work-up: the mixture was concentrated in vacuo. The residue was cautiously poured into ice water, neutralized with saturated aqueous NaHCO3 (50 mL) and extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine (30 mL), dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 0.87 g (94%) of the product as a gray solid.
A 50 mL round bottom flask was charged with 4,8-dichloropyrrolo[1,2-a]quinoxaline (0.40 g, 1.7 mmol), 1-methylpiperazine (0.51 g, 5.1 mmol) and THF (10 mL). The mixture was heated at 60° C. for 12 h and then cooled to room temperature. It was diluted with water (20 mL) and extracted with dichloromethane (20 mL×3). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 1% methanol in dichloromethane, to afford 0.47 g (92%) of the product as an off-white solid. 1H NMR (300 MHz, CDCl3) δ: 7.73 (dd, J=2.7, 1.5 Hz, 1H), 7.70 (d, J=2.1 Hz, 1H), 7.57 (d, J=8.7 Hz, 1H), 7.26 (dd, J=8.7, 2.1 Hz, 1H), 6.90-6.60 (m, 2H), 3.83 (t, J=5.1 Hz, 4H), 2.61 (t, J=5.1 Hz, 4H), 2.38 (s, 3H). MS m/z: 301 (M+H+).
The HCl salt of the title compound was prepared as described in Example 515, except that 1-Boc-piperazine was substituted for 1-methylpiperazine in step 4 of that route. The Boc group was removed by HCl/THF solution. 1H NMR (300 MHz, D2O) δ: 7.91 (dd, J=2.7, 1.2 Hz, 1H), 7.57 (d, J=2.1 Hz, 1H), 7.44 (dd, J=4.5, 1.2 Hz, 1H), 7.35 (d, J=8.7 Hz, 1H), 7.15 (dd, J=8.7, 2.1 Hz, 1H), 6.93 (dd, J=4.5, 2.7 Hz, 1H), 4.19 (t, J=5.4 Hz, 4H), 3.53 (t, J=5.4 Hz, 4H). MS m/z: 287 (M+H+).
A 50 mL round bottom flask was charged with 4-chloro-2-iodoaniline (1.01 g, 4.0 mmol), di-tert-butyl dicarbonate (1.04 g, 4.8 mmol), 4-dimethylaminopyridine (0.49 g, 4.0 mmol) and pyridine (15 mL). The mixture was stirred at 70° C. for 2 h. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:20, Rf=0.7). Work-up: the solvent was evaporated. The residue was mixed with brine and extracted with EtOAc. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 1.08 g (76%) of the product. MS m/z: 354 (M+H+).
A 100 mL round bottom flask was charged with tert-butyl (4-chloro-2-iodophenyl)carbamate (1.24 g, 3.5 mmol), Pd(PPh3)4 (202 mg, 0.17 mmol), Cs2CO3 (1.15 g, 3.5 mmol), 1,4-dioxane (36 mL), water (12 mL) and (1-(tert-butoxycarbonyl)-1H-pyrrol-2-yl)boronic acid (886 mg, 4.2 mmol). The resulting mixture was stirred under N2 atmosphere at 90° C. overnight. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:10). Work-up: the reaction mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 5-10% EtOAc in petroleum ether, to afford 0.324 g (31%) of the product, together with 0.665 g (48%) of tert-butyl 2-(2-((tert-butoxycarbonyl)amino)-5-chlorophenyl)-1H-pyrrole-1-carboxylate.
A 50 mL round bottom flask was charged with tert-butyl (4-chloro-2-(1H-pyrrol-2-yl)phenyl)carbamate (0.324 g, 1.1 mmol) and trifluoroacetic acid (15 mL). The solution was stirred at 25° C. for 2 h. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:4). Work-up: the solvent was evaporated. The residue was mixed with saturated aqueous NaHCO3 and extracted with EtOAc (30 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo, to afford 0.21 g (quantitative) of the product. MS m/z: 193 (M+H+).
A 50 mL round bottom flask was charged with 4-chloro-2-(1H-pyrrol-2-yl)aniline (210 mg, 1.09 mmol), K2CO3 (228 mg, 1.65 mmol), triphosgene (420 mg, 1.42 mmol) and THF (20 mL). The mixture was stirred at 75° C. for 20 h. Reaction progress was monitored by TLC (MeOH/CH2Cl2=1:20, Rf=0.3). Work-up: the solvent was evaporated. The residue was washed with water and dried to afford 166 mg (70%) of the product as a solid. MS m/z: 219 (M+H+).
A 50 mL round bottom flask was charged with 9-chloropyrrolo[1,2-c]quinazolin-5(6H)-one (166 mg, 0.76 mmol), phosphorus oxychloride (15 mL) and diisopropylethylamine (100 mg, 0.76 mmol). The resulting mixture was heated at reflux overnight. Work-up: the reaction mixture was concentrated in vacuo. The residue was cautiously poured into ice water, neutralized with saturated aqueous NaHCO3 and extracted with EtOAc. The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 10% EtOAc in petroleum ether, to afford 60 mg (33%) of the product. MS m/z: 237 (M+H+).
A 50 mL round bottom flask was charged with 5,9-dichloropyrrolo[1,2-c]quinazoline (60 mg, 0.25 mmol), 1-methylpiperazine (76 mg, 0.76 mmol) and THF (10 mL). The mixture was stirred at 60° C. for 1 h. Reaction progress was monitored by TLC. Work-up: the solvent was evaporated. The residue was purified by preparative-TLC, to afford 14 mg (18%) of the product. 1H NMR (300 MHz, CDCl3) δ: 7.84 (d, J=2.4 Hz, 1H), 7.57 (d, J=8.7 Hz, 1H), 7.34 (dd, J=3.0, 1.5 Hz, 1H), 7.31 (dd, J=8.7, 2.4 Hz, 1H), 6.88 (dd, J=3.6, 1.5 Hz, 1H), 6.76 (dd, J=3.6, 3.0 Hz, 1H), 3.48 (t, J=5.0 Hz, 4H), 2.66 (t, J=5.0 Hz, 4H), 2.40 (s, 3H). MS m/z: 301 (M+H+).
The title compound was prepared as described in Example 12.
A 100 mL 3-necked round bottom flask was charged with NaH (383 mg, 9.42 mmol) and THF (20 mL). To the above suspension was added dropwise a solution of diethyl 2-acetamidomalonate (1.40 g, 6.42 mmol) in THF (10 mL) at 0° C. The mixture was allowed to warm to room temperature and stirred for 0.5 h at that temperature. A solution of 2,4,6-trichloroquinazoline (1.00 g, 4.28 mmol) in THF (10 mL) was then added dropwise at 0° C. The resulting solution was stirred at room temperature for 2 h, followed by the addition of N-methylpiperazine (556 mg, 5.56 mmol) and triethylamine (1.55 g, 12.8 mmol). The reaction solution was stirred at room temperature for another 2 h. Work-up: the reaction mixture was diluted with water and extracted with EtOAc. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 2% methanol in CH2Cl2, to afford 1.18 g (57%) of the product as a red solid.
A 25 mL round bottom flask was charged with diethyl 2-acetamido-2-(6-chloro-2-(4-methylpiperazin-1-yl)quinazolin-4-yl)malonate (0.86 g, 1.80 mmol), 8 M aqueous NaOH (0.90 mL, 7.20 mmol) and ethanol (3 mL). The resulting mixture was stirred at room temperature for 2 h then cooled to 5° C. and acidified to pH 2 with 6 M aqueous HCl. Ethanol was evaporated and to the residue was added more 6 M aqueous HCl (1.3 mL). The resulting suspension was stirred at 80° C. for 4 h then room temperature overnight. Work-up: the reaction mixture was basified to pH 10 and extracted with CH2Cl2. The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 5%-20% methanol in CH2Cl2, to afford 250 mg (47%) of the product as a solid. 1H NMR (300 MHz, CDCl3) δ: 7.72-7.71 (m, 1H), 7.57-7.50 (m, 2H), 4.31 (s, 2H), 4.02 (t, J=5.2 Hz, 4H), 2.52 (t, J=5.2 Hz, 4H), 2.36 (s, 3H).
A 10 mL round bottom flask was charged with formic acid (0.5 mL) and acetic anhydride (0.5 mL). The resulting solution was heated at 50° C. for 0.5 h then cooled to room temperature. It was then added into a solution of (6-chloro-2-(4-methylpiperazin-1-yl)quinazolin-4-yl)methanamine (230 mg, 0.788 mmol) in dichloromethane (5 mL). The reaction solution was stirred at room temperature overnight. Work-up: the solvent was evaporated and the residue was purified by flash column chromatography on silica gel with 2%-5% methanol in CH2Cl2, to afford 107 mg (42%) of the product as a light yellow solid.
A 10 mL round bottom flask was charged with N-((6-chloro-2-(4-methylpiperazin-1-yl)quinazolin-4-yl)methyl)formamide (0.100 g, 0.313 mmol) and POCl3 (5 mL). The resulting solution was heated at reflux for 1 h. Work-up: the solvent was evaporated and the residue was purified by flash column chromatography on silica gel with 10% methanol in CH2Cl2, to afford 8 mg (8%) of the product as a light yellow solid. 1H NMR (400 MHz, CDCl3) δ: 8.17 (s, 1H), 7.86 (d, J=2.4 Hz, 1H), 7.76 (s, 1H), 7.59 (d, J=8.6 Hz, 1H), 7.39 (dd, J=8.6, 2.4 Hz, 1H), 3.55 (t, J=4.6 Hz, 4H), 2.69 (t, J=4.6 Hz, 4H), 2.42 (s, 3H). MS m/z: 302 (M+H+).
The HCl salt of the title compound was prepared analogously to Example 501. 1H NMR (300 MHz, D2O/DMSO-d6) δ: 8.53 (s, 1H), 7.86-7.74 (m, 2H), 7.34 (s, 1H), 4.28 (br, 4H), 3.34 (br, 4H), 2.40 (s, 3H). MS m/z: 336 (M+H+).
The following compounds, represented as structures or as SMILES strings below, can generally be made using the methods known in the art and/or as shown above. It is expected that these compounds when made will have activity similar to those that have been made in the examples above. Some of these compounds may have been made and tested, and if so, are represented above in the Examples; if any discrepancy in nomenclature occurs, the Examples control.
The following compounds are represented herein using the Simplified Molecular Input Line Entry System, or SMILES. SMILES is a modern chemical notation system, developed by David Weininger and Daylight Chemical Information Systems, Inc., that is built into all major commercial chemical structure drawing software packages. Software is not needed to interpret SMILES text strings, and an explanation of how to translate SMILES into structures can be found in Weininger, D., J. Chem. Inf. Comput. Sci. 1988, 28, 31-36. All SMILES strings used herein, as well as numerous IUPAC names, were generated using CambridgeSoft's ChemDraw ChemBioDraw Ultra 11.0.
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FC5=CC(═CC1=C5(N═C(C=2N═CSC1=2)N3CCN4CCCC4(C3)))C(F)(F)F CN1CCN(CC1)C4=NC=2C(F)═C(F)C(═CC=2C3=C4(N═CS3))C(F)(F)F FC4=C(F)C(═CC1=C4(N═C(C=2N═CSC1=2)N3CCNCC3))C(F)(F)F FC5=C(F)C(═CC1=C5(N═C(C=2N═CSC1=2)N3CCN4CCCC4(C3)))C(F)(F)F CN1CCN(CC1)C4=NC=2C═C(C(═CC=2C3=C4(N═CS3))C(F)(F)F)C1FC(F)(F)C1=CC2=C(C═C1C1)N═C(C=3N═CSC2=3)N4CCNCC4FC(F)(F)C1=CC2=C(C═C1C1)N═C(C=3N═CSC2=3)N4CCN5CCCC5(C4) CN1CCN(CC1)C4=NC=2C═C(F)C(═CC=2C3=CC═NN34)Br FC2=CC=3N═C(N1CCNCC1)N4N═CC═C4(C=3(C═C2Br)) FC3=CC=4N═C(N1CCN2CCCC2(C1))N5N═CC═C5(C=4(C═C3Br)) CN1CCN(CC1)C4=NC=2C═CC(═CC=2C3=CC═NN34)Br C=2C═C3C=4C═C(C═CC=4(N═C(N1CCNCC1)N3(N=2)))Br C1CC2CN(CCN2(C1))C5=NC=3C═CC(═CC=3C4=CC═NN45)Br CN1CCN(CC1)C3=NC=4C(F)═CC(═CC=4(C2=CC═NN23))Br FC2=CC(═CC=3C1=CC═NN1C(═NC2=3)N4CCNCC4)Br FC2=CC(═CC=3C1=CC═NN1C(═NC2=3)N4CCN5CCCC5(C4))Br CN1CCN(CC1)C3=NC=4C(F)═C(F)C(═CC=4(C2=CC═NN23))Br FC2=C(F)C(═CC=3C1=CC═NN1C(═NC2=3)N4CCNCC4)Br FC2=C(F)C(═CC=3C1=CC═NN1C(═NC2=3)N4CCN5CCCC5(C4))Br 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C1=CC=2C=4C═C(C═CC=4(N═C(C=2(N═N1))N3CCNCC3))C1CN1CCN(CC1)C4=NC=2C═CC(═CC=2C=3C═CN═NC=34)C1C1CC2CN(CCN2(C1))C5=NC=3C═CC(═CC=3C=4C═CN═NC=45)C1FC1=CC=2N═C(C=3N═NC═CC=3(C=2(C═C1C1)))N4CCNCC4CN1CCN(CC1)C4=NC=2C═C(F)C(═CC=2C=3C═CN═NC=34)C1FC1=CC=2N═C(C=3N═NC═CC=3 (C=2(C═C1C1)))N4CCN5CCCC5(C4) FC2=CC(═CC=3C=1C═CN═NC=1C(═NC2=3)N4CCNCC4)C1CN1CCN(CC1)C3=NC=4C(F)═CC(═CC=4(C=2C═CN═NC=23))C1FC2=CC(═CC=3C=1C═CN═NC=1C(═NC2=3)N4CCN5CCCC5(C4))C1FC2=C(F)C(═CC=3C=1C═CN═NC=1C(═NC2=3)N4CCNCC4)C1CN1CCN(CC1)C3=NC=4C(F)═C(F)C(═CC=4(C=2C═CN═NC=23))C1FC2=C(F)C(═CC=3C=1C═CN═NC=1C(═NC2=3)N4CCN5CCCC5(C4))C1FC(F)(F)C1=CC2=C(C═C1C1)N═C(C=3N═NC═CC2=3)N4CCNCC4CN1CCN(CC1)C4=NC=2C═C(C(═CC=2C=3C═CN═NC=34)C(F)(F)F)C1FC(F)(F)C1=CC2=C(C═C1C1)N═C(C=3N═NC═CC2=3)N4CCN5CCCC5(C4) FC(F)(F)C(F)(F)C1=CC═C2N═C(C3=NN═CN3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC═C(C═C2N4C═NN═C34)C(F)(F)C(F)(F)F FC(F)(F)C(F)(F)C1=CC═C2N═C(C3=NN═CN3(C2(=C1)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C3=NN═CN3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC(F)═C(C═C2N4C═NN═C34)C(F)(F)C(F)(F)F FC=1C═C2N═C(C3=NN═CN3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCN5CCCC5(C4) FC=4C═C(C═C1C=4(N═C(C2=NN═CN12)N3CCNCC3))C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C═C(C═C2N4C═NN═C34)C(F)(F)C(F)(F)F FC=5C═C(C═C1C=5(N═C(C2=NN═CN12)N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F FC=4C(F)═C(C═C1C=4(N═C(C2=NN═CN12)N3CCNCC3))C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4C═NN═C34)C(F)(F)C(F)(F)F FC=5C(F)═C(C═C1C=5(N═C(C2=NN═CN12)N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F N#CC1=CC═C2N═C(C3=NN═CN3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC═C(C#N)C═C2N4C═NN═C34 N#CC1=CC═C2N═C(C3=NN═CN3(C2(=C1)))N4CCN5CCCC5(C4) N#CC=1C═C2C(═CC=1(F))N═C(C3=NN═CN23)N4CCNCC4CN1CCN(CC1)C3=NC2=CC(F)═C(C#N)C═C2N4C═NN═C34 N#CC=1C═C2C(═CC=1(F))N═C(C3=NN═CN23)N4CCN5CCCC5(C4) N#CC=4C═C1C(N═C(C2=NN═CN12)N3CCNCC3)=C(F)C=4(F) CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C#N)C═C2N4C═NN═C34 N#CC=5C═C1C(N═C(C2=NN═CN12)N3CCN4CCCC4(C3))=C(F)C=5(F) FC=4C(F)═C(C═C1C=4(N═C(C2=NN═CN12)N3CCNCC3))Br CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4C═NN═C34)Br FC=5C(F)═C(C═C1C=5(N═C(C2=NN═CN12)N3CCN4CCCC4(C3)))Br FC=4C(F)═C(C═C1C=4(N═C(C2=NN═CN12)N3CCNCC3))C1CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4C═NN═C34)C1FC=5C(F)═C(C═C1C=5(N═C(C2=NN═CN12)N3CCN4CCCC4(C3)))C1FC=4C(F)═C(C═C1C=4(N═C(C2=NN═CN12)N3CCNCC3))C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4C═NN═C34)C(F)(F)F FC=5C(F)═C(C═C1C=5(N═C(C2=NN═CN12)N3CCN4CCCC4(C3)))C(F)(F)F CC1=CC(F)═C2N═C(C3=NN═CN3(C2(=C1)))N4CCNCC4CC1=CC(F)═C2N═C(C3=NN═CN3(C2(=C1)))N4CCN(C)CC4CC1=CC(F)═C2N═C(C3=NN═CN3(C2(=C1)))N4CCN5CCCC5(C4) CC=4C═C1C(N═C(C2=NN═CN12)N3CCNCC3)=C(F)C=4(F) CC=4C═C1C(N═C(C2=NN═CN12)N3CCN(C)CC3)=C(F)C=4(F) CC=5C═C1C(N═C(C2=NN═CN12)N3CCN4CCCC4(C3))=C(F)C=5(F) FC=4C═C1C(N═C(C2=NN═CN12)N3CCNCC3)=C(F)C=4(F) CN1CCN(CC1)C3=NC2=C(F)C(F)═C(F)C═C2N4C═NN═C34 FC=5C═C1C(N═C(C2=NN═CN12)N3CCN4CCCC4(C3))=C(F)C=5(F) FC(F)(F)C=1C═C2N═C(C3=NN═CN3(C2(=CC=1C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC(═C(C═C2N4C═NN═C34)C(F)(F)F)C(F)(F)F FC(F)(F)C=1C═C2N═C(C3=NN═CN3(C2(=CC=1C(F)(F)F)))N4CCN5CCCC5(C4) FC2(F)(C=1C═C3N═C(C4=NN═CN4(C3(=CC=1C(F)(F)C2(F)(F))))N5CCNCC5) CN1CCN(CC1)C3=NC2=CC5=C(C═C2N4C═NN═C34)C(F)(F)C(F)(F)C5(F)(F) FC2(F)(C=1C═C3N═C(C4=NN═CN4(C3(=CC=1C(F)(F)C2(F)(F))))N5CCN6CCCC6(C5)) CC=2N═C3C4=CC(═CC═C4(N═C(N1CCNCC1)N3(N=2)))C(F)(F)C(F)(F)F CC=2N═C3C4=CC(═CC═C4(N═C(N1CCN(C)CC1)N3(N=2)))C(F)(F)C(F)(F)F CC=3N═C4C5=CC(═CC═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))C(F)(F)C(F)(F)F CC=2N═C3C4=CC(═C(F)C═C4(N═C(N1CCNCC1)N3(N=2)))C(F)(F)C(F)(F)F CC=2N═C3C4=CC(═C(F)C═C4(N═C(N1CCN(C)CC1)N3(N=2)))C(F)(F)C(F)(F)F CC=3N═C4C5=CC(═C(F)C═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))C(F)(F)C(F)(F)F CC=2N═C3C4=CC(═CC(F)═C4(N═C(N1CCNCC1)N3(N=2)))C(F)(F)C(F)(F)F CC=2N═C3C4=CC(═CC(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)))C(F)(F)C(F)(F)F CC=3N═C4C5=CC(═CC(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))C(F)(F)C(F)(F)F CC=2N═C3C4=CC(═C(F)C(F)═C4(N═C(N1CCNCC1)N3(N=2)))C(F)(F)C(F)(F)F CC=2N═C3C4=CC(═C(F)C(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)))C(F)(F)C(F)(F)F CC=3N═C4C5=CC(═C(F)C(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))C(F)(F)C(F)(F)F CC=2N═C3C4=CC(C#N)=C(F)C═C4(N═C(N1CCNCC1)N3(N=2)) CC=2N═C3C4=CC(C#N)=C(F)C═C4(N═C(N1CCN(C)CC1)N3(N=2)) CC=3N═C4C5=CC(C#N)=C(F)C═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)) CC=2N═C3C4=CC(C#N)=CC═C4(N═C(N1CCNCC1)N3(N=2)) CC=2N═C3C4=CC(C#N)=CC═C4(N═C(N1CCN(C)CC1)N3(N=2)) CC=3N═C4C5=CC(C#N)=CC═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)) CC=2N═C3C4=CC(C#N)=CC(F)═C4(N═C(N1CCNCC1)N3(N=2)) CC=2N═C3C4=CC(C#N)=CC(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)) CC=3N═C4C5=CC(C#N)=CC(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)) CC=2N═C3C4=CC(C#N)=C(F)C(F)═C4(N═C(N1CCNCC1)N3(N=2)) CC=2N═C3C4=CC(C#N)=C(F)C(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)) CC=3N═C4C5=CC(C#N)=C(F)C(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)) CC=2N═C3C4=CC(═C(F)C(F)═C4(N═C(N1CCNCC1)N3(N=2)))Br CC=2N═C3C4=CC(═C(F)C(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)))Br CC=3N═C4C5=CC(═C(F)C(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))Br CC=2N═C3C4=CC(═C(F)C(F)═C4(N═C(N1CCNCC1)N3(N=2)))C1CC=2N═C3C4=CC(═C(F)C(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)))C1CC=3N═C4C5=CC(═C(F)C(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))C1CC=2N═C3C4=CC(═C(F)C(F)═C4(N═C(N1CCNCC1)N3(N=2)))C(F)(F)F CC=2N═C3C4=CC(═C(F)C(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)))C(F)(F)F CC=3N═C4C5=CC(═C(F)C(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))C(F)(F)F CC=2N═C3C4=CC(C)=C(F)C═C4(N═C(N1CCNCC1)N3(N=2)) CC=2N═C3C4=CC(C)=C(F)C═C4(N═C(N1CCN(C)CC1)3(N=2)) CC=3N═C4C5=CC(C)=C(F)C═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)) CC2=CC(F)═C3N═C(N1CCNCC1)N4N═C(C)N═C4(C3(=C2)) CC2=CC(F)═C3N═C(N1CCN(C)CC1)N4N═C(C)N═C4(C3(=C2)) CC3=CC(F)═C4N═C(N1CCN2CCCC2(C1))N5N═C(C)N═C5(C4(=C3)) CC=2N═C3C4=CC(C)=C(F)C(F)═C4(N═C(N1CCNCC1)N3(N=2)) CC=2N═C3C4=CC(C)=C(F)C(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)) CC=3N═C4C5=CC(C)=C(F)C(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)) CC=2N═C3C4=CC(F)═C(F)C(F)═C4(N═C(N1CCNCC1)N3(N=2)) CC=2N═C3C4=CC(F)═C(F)C(F)═C4(N═C(N1CCN(C)CC1)N3(N=2)) CC=3N═C4C5=CC(F)═C(F)C(F)═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)) CC=2N═C3C4=CC(═C(C═C4(N═C(N1CCNCC1)N3(N=2)))C(F)(F)F)C(F)(F)F CC=2N═C3C4=CC(═C(C═C4(N═C(N1CCN(C)CC1)N3(N=2)))C(F)(F)F)C(F)(F)F CC=3N═C4C5=CC(═C(C═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))C(F)(F)F)C(F)(F)F CC=2N═C3C4=CC5=C(C═C4(N═C(N1CCNCC1)N3(N=2)))C(F)(F)C(F)(F)C5(F)(F) CC=2N═C3C4=CC5=C(C═C4(N═C(N1CCN(C)CC1)N3(N=2)))C(F)(F)C(F)(F)C5(F)(F) CC=3N═C4C5=CC6=C(C═C5(N═C(N1CCN2CCCC2(C1))N4(N=3)))C(F)(F)C(F)(F) C6(F)(F) FC(F)(F)C(F)(F)C1=CC═C2N═C(C3=NN═NN3(C2(=C1)))N4CCNCC4FC=1C═C2N═C(C3=NN═NN3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCNCC4FC=4C═C(C═C1C=4(N═C(C2=NN═NN12)N3CCNCC3))C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC2=CC═C(C═C2N4N═NN═C34)C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC2=CC(F)═C(C═C2N4N═NN═C34)C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C═C(C═C2N4N═NN═C34)C(F)(F)C(F)(F)F FC(F)(F)C(F)(F)C1=CC═C2N═C(C3=NN═NN3(C2(=C1)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C3=NN═NN3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCN5CCCC5(C4) FC=5C═C(C═C1C=5(N═C(C2=NN═NN12)N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F FC=4C(F)═C(C═C1C=4(N═C(C2=NN═NN12)N3CCNCC3))C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4N═NN═C34)C(F)(F)C(F)(F)F FC=5C(F)═C(C═C1C=5(N═C(C2=NN═NN12)N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC2=CC═C(C#N)C═C2N4N═NN═C34 N#CC=1C═C2C(═CC=1(F))N═C(C3=NN═NN23)N4CCNCC4CN1CCN(CC1)C3=NC2=CC(F)═C(C#N)C═C2N4N═NN═C34 N#CC=1C═C2C(═CC=1(F))N═C(C3=NN═NN23)N4CCN5CCCC5(C4) N#CC1=CC(F)═C2N═C(C3=NN═NN3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C3=NC2=C(F)C═C(C#N)C═C2N4N═NN═C34 N#CC1=CC(F)═C2N═C(C3=NN═NN3(C2(=C1)))N4CCN5CCCC5(C4) N#CC=4C═C1C(N═C(C2=NN═NN12)N3CCNCC3)=C(F)C=4(F) CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C#N)C═C2N4N═NN═C34 N#CC=5C═C1C(N═C(C2=NN═NN12)N3CCN4CCCC4(C3))=C(F)C=5(F) FC=4C(F)═C(C═C1C=4(N═C(C2=NN═NN12)N3CCNCC3))Br CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4N═NN═C34)Br FC=5C(F)═C(C═C1C=5(N═C(C2=NN═NN12)N3CCN4CCCC4(C3)))Br CC1=CC(F)═C2N═C(C3=NN═NN3(C2(=C1)))N4CCNCC4CC=4C═C1C(N═C(C2=NN═NN12)N3CCNCC3)=C(F)C=4(F) FC=4C═C1C(N═C(C2=NN═NN12)N3CCNCC3)=C(F)C=4(F) FC2(F)(C=1C═C3N═C(C4=NN═NN4(C3(=CC=1C(F)(F)C2(F)(F))))N5CCNCC5) FC(F)(F)OC1=CC═C2N═C(C3=NN═NN3(C2(=C1)))N4CCNCC4 CN1CCN(CC1)C3=NC2=CC═C(C═C2N4N═NN═C34)OC(F)(F)F FC(F)(F)OC1=CC═C2N═C(C3=NN═NN3(C2(=C1)))N4CCN5CCCC5(C4) FC(F)(F)C1=CC═C2N═C(C3=NN═NN3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC═C(C═C2N4N═NN═C34)C(F)(F)F FC(F)(F)C1=CC═C2N═C(C3=NN═NN3(C2(=C1)))N4CCN5CCCC5(C4) CN1CCN(CC1)C3=NC2=CC5=C(C═C2N4N═NN═C34)C(F)(F)C(F)(F)C5(F)(F) FC2(F)(C=1C═C3N═C(C4=NN═NN4(C3(=CC=1C(F)(F)C2(F)(F))))N5CCN6CCCC6(C5)) CC1=CC(F)═C2N═C(C3=NN═NN3(C2(=C1)))N4CCN(C)CC4CC=4C═C1C(N═C(C2=NN═NN12)N3CCN(C)CC3)=C(F)C=4(F) CN1CCN(CC1)C3=NC2=C(F)C(F)═C(F)C═C2N4N═NN═C34 CC1=CC(F)═C2N═C(C3=NN═NN3(C2(=C1)))N4CCN5CCCC5(C4) CC=5C═C1C(N═C(C2=NN═NN12)N3CCN4CCCC4(C3))=C(F)C=5(F) FC=5C═C1C(N═C(C2=NN═NN12)N3CCN4CCCC4(C3))=C(F)C=5(F) FC=4C(F)═C(C═C1C=4(N═C(C2=NN═NN12)N3CCNCC3))C1CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4N═NN═C34)C1FC=5C(F)═C(C═C1C=5(N═C(C2=NN═NN12)N3CCN4CCCC4(C3)))C1FC=4C(F)═C(C═C1C=4(N═C(C2=NN═NN12)N3CCNCC3))C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4N═NN═C34)C(F)(F)F FC=5C(F)═C(C═C1C=5(N═C(C2=NN═NN12)N3CCN4CCCC4(C3)))C(F)(F)F CC=1C═C2C(═CC=1(F))N═C(C3=NN═NN23)N4CCNCC4CC=1C═C2C(═CC=1(F))N═C(C3=NN═NN23)N4CCN(C)CC4CC=1C═C2C(═CC=1(F))N═C(C3=NN═NN23)N4CCN5CCCC5(C4) CC=2N═C3C(═NC1=CC═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCNCC4CC=2N═C3C(═NC1=CC═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCN(C)CC4CC=2N═C3C(═NC1=CC═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCN5CCCC5(C4) CC=2N═C3C(═NC1=CC(F)═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCNCC4CC=2N═C3C(═NC1=CC(F)═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCN(C)CC4CC=2N═C3C(═NC1=CC(F)═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCN5CCCC5(C4) CC=2N═C3C(═NC1=C(F)C═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCNCC4CC=2N═C3C(═NC1=C(F)C═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCN(C)CC4CC=2N═C3C(═NC1=C(F)C═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCN5CCCC5(C4) CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCNCC4CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))C(F)(F)C(F)(F)F)N4CCN(C)CC4CC=2N═C3C(═NC1=CC═C(C#N)C═C1N3(N=2))N4CCNCC4CC=2N═C3C(═NC1=C(F)C═C(C#N)C═C1N3(N=2))N4CCNCC4CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))Br)N4CCNCC4CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))Br)N4CCN(C)CC4CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))Br)N4CCN5CCCC5(C4) CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))C1)N4CCNCC4CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))C1)N4CCN(C)CC4CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))C1)N4CCN5CCCC5(C4) CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))C(F)(F)F)N4CCNCC4CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))C(F)(F)F)N4CCN(C)CC4CC=2N═C3C(═NC1=C(F)C(F)═C(C═C1N3(N=2))C(F)(F)F)N4CCN5CCCC5(C4) CC=2N═C3C(═NC1=CC(F)═C(C═C1N3(N=2))C(F)(F)F)N4CCNCC4CC=2N═C3C(═NC1=CC(F)═C(C═C1N3(N=2))C(F)(F)F)N4CCN(C)CC4CC=2N═C3C(═NC1=CC(F)═C(C═C1N3(N=2))C(F)(F)F)N4CCN5CCCC5(C4) FC(F)(F)C(F)(F)C1=CC═C2N═C(C3=NC═NN3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC═C(C═C2N4N═CN═C34)C(F)(F)C(F)(F)F 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FC=1C(F)═C2N═C(C3=NOC═C3(C2(=CC=1Br)))N4CCNCC4CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CON═C23))Br FC=1C(F)═C2N═C(C3=NOC═C3(C2(=CC=1Br)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C3=NOC═C3(C2(=CC=1C1)))N4CCNCC4FC=1C═C2N═C(C3=NOC═C3(C2(=CC=1C1)))N4CCN5CCCC5(C4) FC=2C═C(C═C3C1=CON═C1C(═NC=23)N4CCNCC4)C1CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CON═C23))C1FC=2C═C(C═C3C1=CON═C1C(═NC=23)N4CCN5CCCC5(C4))C1FC=1C(F)═C2N═C(C3=NOC═C3(C2(=CC=1C1)))N4CCNCC4CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CON═C23))C1FC=1C(F)═C2N═C(C3=NOC═C3(C2(=CC=1C1)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C3=NOC═C3(C2(=CC=1C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CON═C34)C(F)(F)F FC=1C═C2N═C(C3=NOC═C3(C2(=CC=1C(F)(F)F)))N4CCN5CCCC5(C4) FC=2C═C(C═C3C1=CON═C1C(═NC=23)N4CCNCC4)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CON═C23))C(F)(F)F FC=2C═C(C═C3C1=CON═C1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)F FC=1C(F)═C2N═C(C3=NOC═C3(C2(=CC=1C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CON═C23))C(F)(F)F 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CN1CCN(CC1)C4=NC2=C(F)C(F)═C(C═C2C3=NN═NN34)C(F)(F)F FC=5C(F)═C(C═C3C=5(N═C(N1CCN2CCCC2(C1))N4N═NN═C34))C(F)(F)F CC=1C═C3C(═CC=1(F))N═C(N2CCNCC2)N4N═NN═C34 CC=1C═C3C(═CC=1(F))N═C(N2CCN(C)CC2)N4N═NN═C34 CC=1C═C4C(═CC=1(F))N═C(N2CCN3CCCC3(C2))N5N═NN═C45 CC2=CC(F)═C3N═C(N1CCNCC1)N4N═NN═C4(C3(=C2)) CC2=CC(F)═C3N═C(N1CCN(C)CC1)N4N═NN═C4(C3(=C2)) CC3=CC(F)═C4N═C(N1CCN2CCCC2(C1))N5N═NN═C5(C4(=C3)) CC2=NC=3C(═NC1=CC(F)═C(C═C1C=3(O2))Br)N4CCNCC4CC2=NC=3C(═NC1=CC(F)═C(C═C1C=3(O2))Br)N4CCN(C)CC4CC2=NC=3C(═NC1=CC(F)═C(C═C1C=3(O2))Br)N4CCN5CCCC5(C4) CC2=NC=3C(═NC1=C(F)C═C(C═C1C=3(O2))Br)N4CCNCC4CC2=NC=3C(═NC1=C(F)C═C(C═C1C=3(O2))Br)N4CCN(C)CC4CC2=NC=3C(═NC1=C(F)C═C(C═C1C=3(O2))Br)N4CCN5CCCC5(C4) CC2=NC=3C(═NC1=C(F)C(F)═C(C═C1C=3(O2))Br)N4CCNCC4CC2=NC=3C(═NC1=C(F)C(F)═C(C═C1C=3(O2))Br)N4CCN(C)CC4CC2=NC=3C(═NC1=C(F)C(F)═C(C═C1C=3(O2))Br)N4CCN5CCCC5(C4) CC2=NC=3C(═NC1=CC(F)═C(C═C1C=3(O2))C1)N4CCNCC4CC2=NC=3C(═NC1=CC(F)═C(C═C1C=3(O2))C1)N4CCN(C)CC4CC2=NC=3C(═NC1=CC(F)═C(C═C1C=3(O2))C1)N4CCN5CCCC5(C4) CC2=NC=3C(═NC1=C(F)C═C(C═C1C=3(O2))C1)N4CCNCC4CC2=NC=3C(═NC1=C(F)C═C(C═C1C=3(O2))C1)N4CCN(C)CC4CC2=NC=3C(═NC1=C(F)C═C(C═C1C=3 (O2))C1)N4CCN5CCCC5(C4) CC2=NC=3C(═NC1=C(F)C(F)═C(C═C1C=3(O2))C1)N4CCNCC4CC2=NC=3C(═NC1=C(F)C(F)═C(C═C1C=3(O2))C1)N4CCN(C)CC4CC2=NC=3C(═NC1=C(F)C(F)═C(C═C1C=3(O2))C1)N4CCN5CCCC5(C4) FC(F)(F)C(F)(F)C1=CC═C2N═C(C=3N═COC=3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC═C(C═C2C=4OC═NC3=4)C(F)(F)C(F)(F)F FC(F)(F)C(F)(F)C1=CC═C2N═C(C=3N═COC=3(C2(=C1)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C=3N═COC=3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC(F)═C(C═C2C=4OC═NC3=4)C(F)(F)C(F)(F)F FC=1C═C2N═C(C=3N═COC=3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCN5CCCC5(C4) FC=4C═C(C═C1C=4(N═C(C=2N═COC1=2)N3CCNCC3))C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C═C(C═C2C=4OC═NC3=4)C(F)(F)C(F)(F)F FC=5C═C(C═C1C=5(N═C(C=2N═COC1=2)N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F FC=1C═C2N═C(C=3N═COC=3(C2(=CC=1Br)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC(F)═C(C═C2C=4OC═NC3=4)Br FC=1C═C2N═C(C=3N═COC=3(C2(=CC=1Br)))N4CCN5CCCC5(C4) 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FC=4C═C(C═C1C=4(N═C(C2=NC═CN12)N3CCNCC3))Br CN1CCN(CC1)C3=NC2=C(F)C═C(C═C2N4C═CN═C34)Br FC=5C═C(C═C1C=5(N═C(C2=NC═CN12)N3CCN4CCCC4(C3)))Br FC=4C(F)═C(C═C1C=4(N═C(C2=NC═CN12)N3CCNCC3))Br CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4C═CN═C34)Br FC=5C(F)═C(C═C1C=5(N═C(C2=NC═CN12)N3CCN4CCCC4(C3)))Br FC=4C═C(C═C1C=4(N═C(C2=NC═CN12)N3CCNCC3))C1CN1CCN(CC1)C3=NC2=C(F)C═C(C═C2N4C═CN═C34)C1FC=5C═C(C═C1C=5(N═C(C2=NC═CN12)N3CCN4CCCC4(C3)))C1FC=4C(F)═C(C═C1C=4(N═C(C2=NC═CN12)N3CCNCC3))C1CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4C═CN═C34)C1FC=5C(F)═C(C═C1C=5(N═C(C2=NC═CN12)N3CCN4CCCC4(C3)))C1FC(F)(F)C1=CC═C2N═C(C3=NC═CN3(C2(=C1)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C3=NC═CN3(C2(=CC=1C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C3=NC2=CC(F)═C(C═C2N4C═CN═C34)C(F)(F)F FC=1C═C2N═C(C3=NC═CN3(C2(=CC=1C(F)(F)F)))N4CCN5CCCC5(C4) FC=4C═C(C═C1C=4(N═C(C2=NC═CN12)N3CCNCC3))C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C═C(C═C2N4C═CN═C34)C(F)(F)F FC=5C═C(C═C1C=5(N═C(C2=NC═CN12)N3CCN4CCCC4(C3)))C(F)(F)F FC=4C(F)═C(C═C1C=4(N═C(C2=NC═CN12)N3CCNCC3))C(F)(F)F CN1CCN(CC1)C3=NC2=C(F)C(F)═C(C═C2N4C═CN═C34)C(F)(F)F FC=5C(F)═C(C═C1C=5(N═C(C2=NC═CN12)N3CCN4CCCC4(C3)))C(F)(F)F CC1=CC═C2N═C(C3=NC═CN3(C2(=C1)))N4CCNCC4 CC1=CC═C2N═C(C3=NC═CN3(C2(=C1)))N4CCN(C)CC4CC1=CC═C2N═C(C3=NC═CN3(C2(=C1)))N4CCN5CCCC5(C4) CC=1C═C2C(═CC=1(F))N═C(C3=NC═CN23)N4CCNCC4CC=1C═C2C(═CC=1(F))N═C(C3=NC═CN23)N4CCN(C)CC4CC=1C═C2C(═CC=1(F))N═C(C3=NC═CN23)N4CCN5CCCC5(C4) FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C3=NC═CN23)N4CCNCC4CN1CCN(CC1)C3=NC2=CC(═C(C═C2N4C═CN═C34)C(F)(F)F)C1FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C3=NC═CN23)N4CCN5CCCC5(C4) FC=1C═C2C(═CC=1C(F)(F)F)N═C(C3=NC═CN23)N4CCNCC4FC2(F)(C=1C═C3N═C(C4=NC═CN4(C3(=CC=1C(F)(F)C2(F)(F))))N5CCNCC5) FC(F)(F)OC1=CC═C2N═C(C3=NC═CN3(C2(=C1)))N4CCNCC4FC(F)(F)C(F)(F)C1=CC═C2N═C(C3=NNC═C3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC═C(C═C2C3=CNN═C34)C(F)(F)C(F)(F)F FC(F)(F)C(F)(F)C1=CC═C2N═C(C3=NNC═C3(C2(=C1)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C3=NNC═C3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CNN═C34)C(F)(F)C(F)(F)F FC=1C═C2N═C(C3=NNC═C3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCN5CCCC5(C4) FC=2C═C(C═C3C1=CNN═C1C(═NC=23)N4CCNCC4)C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CNN═C23))C(F)(F)C(F)(F)F FC=2C═C(C═C3C1=CNN═C1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)C(F)(F)F N#CC1=CC(F)═C2N═C(C3=NNC═C3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C3=NC4=C(F)C═C(C#N)C═C4(C2=CNN═C23) N#CC1=CC(F)═C2N═C(C3=NNC═C3(C2(=C1)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C3=NNC═C3(C2(=CC=1Br)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CNN═C34)Br FC=1C═C2N═C(C3=NNC═C3(C2(=CC=1Br)))N4CCN5CCCC5(C4) FC=2C(F)═C(C═C3C1=CNN═C1C(═NC=23)N4CCNCC4)Br CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CNN═C23))Br FC=2C(F)═C(C═C3C1=CNN═C1C(═NC=23)N4CCN5CCCC5(C4))Br FC=1C═C2N═C(C3=NNC═C3(C2(=CC=1C1)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CNN═C34)C1 FC=1C═C2N═C(C3=NNC═C3(C2(=CC=1C1)))N4CCN5CCCC5(C4) FC=2C═C(C═C3C1=CNN═C1C(═NC=23)N4CCNCC4)C1CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CNN═C23))C1FC=2C═C(C═C3C1=CNN═C1C(═NC=23)N4CCN5CCCC5(C4))C1FC=2C(F)═C(C═C3C1=CNN═C1C(═NC=23)N4CCNCC4)C1CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CNN═C23))C1FC=2C(F)═C(C═C3C1=CNN═C1C(═NC=23)N4CCN5CCCC5(C4))C1FC=1C═C2N═C(C3=NNC═C3(C2(=CC=1C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CNN═C34)C(F)(F)F FC=1C═C2N═C(C3=NNC═C3(C2(=CC=1C(F)(F)F)))N4CCN5CCCC5(C4) FC=2C═C(C═C3C1=CNN═C1C(═NC=23)N4CCNCC4)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CNN═C23))C(F)(F)F FC=2C═C(C═C3C1=CNN═C1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)F FC=2C(F)═C(C═C3C1=CNN═C1C(═NC=23)N4CCNCC4)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CNN═C23))C(F)(F)F FC=2C(F)═C(C═C3C1=CNN═C1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)F FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C3=NNC═C23)N4CCNCC4CN1CCN(CC1)C4=NC2=CC(═C(C═C2C3=CNN═C34)C(F)(F)F)C1FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C3=NNC═C23)N4CCN5CCCC5(C4) CN1CCN(CC1)C4=NC2=CC═C(C═C2C3=CN(C)N═C34)C(F)(F)C(F)(F)F CN1C═C2C5=CC(═CC═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CN(C)N═C34)C(F)(F)C(F)(F)F CN1C═C2C5=CC(═C(F)C═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CN(C)N═C23))C(F)(F)C(F)(F)F CN1C═C2C5=CC(═CC(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CN(C)N═C23))C(F)(F)C(F)(F)F CN1C═C2C5=CC(═C(F)C(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F CN1CCN(CC1)C4=NC2=CC═C(C#N)C═C2C3=CN(C)N═C34 CN1C═C2C5=CC(C#N)=CC═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)) CN1CCN(CC1)C4=NC2=CC(F)═C(C#N)C═C2C3=CN(C)N═C34 CN1C═C2C5=CC(C#N)=C(F)C═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)) CN1CCN(CC1)C3=NC4=C(F)C═C(C#N)C═C4(C2=CN(C)N═C23) CN1C═C2C5=CC(C#N)=CC(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)) CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CN(C)N═C34)Br CN1C═C2C5=CC(═C(F)C═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))Br CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CN(C)N═C23))Br CN1C═C2C5=CC(═CC(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))Br CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CN(C)N═C23))Br CN1C═C2C5=CC(═C(F)C(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))Br CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CN(C)N═C34)C1CN1C═C2C5=CC(═C(F)C═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C1CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CN(C)N═C23))C1CN1C═C2C5=CC(═CC(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C1CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CN(C)N═C23))C1CN1C═C2C5=CC(═C(F)C(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C1CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C3=CN(C)N═C34)C(F)(F)F CN1C═C2C5=CC(═C(F)C═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C2=CN(C)N═C23))C(F)(F)F CN1C═C2C5=CC(═CC(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C2=CN(C)N═C23))C(F)(F)F CN1C═C2C5=CC(═C(F)C(F)═C5(N═C(C2(=N1))N3CCN4CCCC4(C3)))C(F)(F)F CC1=CC═C2N═C(C3=NN(C)C═C3(C2(=C1)))N4CCN(C)CC4CC1=CC═C2N═C(C3=NN(C)C═C3(C2(=C1)))N4CCN5CCCC5(C4) CC=1C═C2C(═CC=1(F))N═C(C3=NN(C)C═C23)N4CCN(C)CC4CC=1C═C2C(═CC=1(F))N═C(C3=NN(C)C═C23)N4CCN5CCCC5(C4) CC1=CC(F)═C2N═C(C3=NN(C)C═C3(C2(=C1)))N4CCN(C)CC4CC1=CC(F)═C2N═C(C3=NN(C)C═C3(C2(=C1)))N4CCN5CCCC5(C4) C1CN(CCN1)C4=NC2=CC═C(C═C2C=3NC═NC=34)Br CN1CCN(CC1)C4=NC2=CC═C(C═C2C=3NC═NC=34)Br C1CC2CN(CCN2(C1))C5=NC3=CC═C(C═C3C=4NC═NC=45)Br FC=1C═C2N═C(C=3N═CNC=3(C2(=CC=1Br)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C=3NC═NC=34)Br FC=1C═C2N═C(C=3N═CNC=3(C2(=CC=1Br)))N4CCN5CCCC5(C4) FC=4C═C(C═C1C=4(N═C(C=2N═CNC1=2)N3CCNCC3))Br CN1CCN(CC1)C4=NC2=C(F)C═C(C═C2C=3NC═NC=34)Br FC=5C═C(C═C1C=5(N═C(C=2N═CNC1=2)N3CCN4CCCC4(C3)))Br FC=1C═C2N═C(C=3N═CNC=3(C2(=CC=1C1)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C=3NC═NC=34)C1FC=1C═C2N═C(C=3N═CNC=3(C2(=CC=1C1)))N4CCN5CCCC5(C4) FC=4C═C(C═C1C=4(N═C(C=2N═CNC1=2)N3CCNCC3))C1CN1CCN(CC1)C4=NC2=C(F)C═C(C═C2C=3NC═NC=34)C1FC=5C═C(C═C1C=5(N═C(C=2N═CNC1=2)N3CCN4CCCC4(C3)))C1CN1CCN(CC1)C4=NC2=CC═C(C═C2C=3NC═NC=34)C(F)(F)F FC(F)(F)C1=CC═C2N═C(C=3N═CNC=3(C2(=C1)))N4CCN5CCCC5(C4) CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C=3NC═NC=34)C(F)(F)F FC=1C═C2N═C(C=3N═CNC=3(C2(=CC=1C(F)(F)F)))N4CCN5CCCC5(C4) CN1CCN(CC1)C4=NC2=C(F)C═C(C═C2C=3NC═NC=34)C(F)(F)F FC=5C═C(C═C1C=5(N═C(C=2N═CNC1=2)N3CCN4CCCC4(C3)))C(F)(F)F FC(F)(C(C1=CC═C(N═C(N4CCNCC4)C3=C2C═NC═N3)C2=C1)(F)F)F FC(F)(F)C(F)(F)C1=CC═C2N═C(C=3N═CC═NC=3(C2(=C1)))N4CCNCC4FC(F)(F)C(F)(F)C1=CC═C2N═C(C=3N═CC═CC=3(C2(=C1)))N4CCNCC4CN(CC4)CCN4C2=NC1=CC═C(C(F)(C(F)(F)F)F)C═C1C3=C2N═CN═C3CN1CCN(CC1)C4=NC2=CC═C(C═C2C=3N═CC═NC=34)C(F)(F)C(F)(F)F CN1CCN(CC1)C4=NC2=CC═C(C═C2C=3C═CC═NC=34)C(F)(F)C(F)(F)F FC(F)(C(C1=CC═C(N═C(N4CCN(CCC5)C5C4)C3=C2C═NC═N3)C2=C1)(F)F)F FC(F)(F)C(F)(F)C1=CC═C2N═C(C=3N═CC═NC=3(C2(=C1)))N4CCN5CCCC5(C4) FC(F)(F)C(F)(F)C1=CC═C2N═C(C=3N═CC═CC=3(C2(=C1)))N4CCN5CCCC5(C4) FC1=C(C(F)(C(F)(F)F)F)C═C2C(N═C(N4CCNCC4)C3=C2C═NC═N3)=C1FC=1C═C2N═C(C=3N═CC═NC=3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCNCC4FC=1C═C2N═C(C=3N═CC═CC=3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCNCC4 CN(CC4)CCN4C2=NC1=CC(F)═C(C(F)(C(F)(F)F)F)C═C1C3=C2N═CN═C3 CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C=3N═CC═NC=34)C(F)(F)C(F)(F)F CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C=3C═CC═NC=34)C(F)(F)C(F)(F)F FC1=C(C(F)(C(F)(F)F)F)C═C2C(N═C(N4CCN(CCC5)C5C4)C3=C2C═NC═N3)=C1FC=1C═C2N═C(C=3N═CC═NC=3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C=3N═CC═CC=3(C2(=CC=1C(F)(F)C(F)(F)F)))N4CCN5CCCC5(C4) FC1=C(N═C(N4CCNCC4)C3=C2C═NC═N3)C2=CC(C(C(F)(F)F)(F)F)═C1FC=4C═C(C═C1C=4(N═C(C=2N═CC═NC1=2)N3CCNCC3))C(F)(F)C(F)(F)F FC=2C═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCNCC4)C(F)(F)C(F)(F)F CN(CC4)CCN4C2=NC1=C(F)C═C(C(C(F)(F)F)(F)F)C═C1C3=C2N═CN═C3 CN1CCN(CC1)C4=NC2=C(F)C═C(C═C2C=3N═CC═NC=34)C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C=2C═CC═NC=23))C(F)(F)C(F)(F)F FC1=C(N═C(N4CCN(CCC5)C5C4)C3=C2C═NC═N3)C2=CC(C(F)(C(F)(F)F)F)═C1FC=5C═C(C═C1C=5(N═C(C=2N═CC═NC1=2)N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F FC=2C═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)C(F)(F)F FC1=C(C(C(F)(F)F)(F)F)C═C2C(N═C(N4CCNCC4)C3=C2C═NC═N3)=C1F FC=4C(F)═C(C═C1C=4(N═C(C=2N═CC═NC1-2)N3CCNCC3))C(F)(F)C(F)(F)F FC=2C(F)═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCNCC4)C(F)(F)C(F)(F)F CN(CC4)CCN4C2=NC1=C(F)C(F)═C(C(F)(C(F)(F)F)F)C═C1C3=C2N═CN═C3 CN1CCN(CC1)C4=NC2=C(F)C(F)═C(C═C2C=3N═CC═NC=34)C(F)(F)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C=2C═CC═NC=23))C(F)(F)C(F)(F)F FC1=C(C(F)(C(F)(F)F)F)C═C2C(N═C(N4CCN(CCC5)C5C4)C3=C2C═NC═N3)=C1F FC=5C(F)═C(C═C1C=5(N═C(C=2N═CC═NC1-2)N3CCN4CCCC4(C3)))C(F)(F)C(F)(F)F FC=2C(F)═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)C(F)(F)F N#CC1=CC═C2N═C(C=3N═CN═CC=3(C2(=C1)))N4CCNCC4 N#CC1=CC═C2N═C(C=3N═CC═NC=3(C2(=C1)))N4CCNCC4N#CC1=CC═C2N═C(C=3N═CC═CC=3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC═C(C#N)C═C2C=3C═NC═NC=34 CN1CCN(CC1)C4=NC2=CC═C(C#N)C═C2C=3N═CC═NC=34 CN1CCN(CC1)C4=NC2=CC═C(C#N)C═C2C=3C═CC═NC=34 N#CC1=CC═C2N═C(C=3N═CN═CC=3(C2(=C1)))N4CCN5CCCC5(C4) N#CC1=CC═C2N═C(C=3N═CC═NC=3(C2(=C1)))N4CCN5CCCC5(C4) N#CC1=CC═C2N═C(C=3N═CC═CC=3(C2(=C1)))N4CCN5CCCC5(C4) N#CC=1C═C2C(═CC=1(F))N═C(C=3N═CN═CC2=3)N4CCNCC4N#CC=1C═C2C(═CC=1(F))N═C(C=3N═CC═NC2=3)N4CCNCC4N#CC=1C═C2C(═CC=1(F))N═C(C=3N═CC═CC2=3)N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C#N)C═C2C=3C═NC═NC=34 CN1CCN(CC1)C4=NC2=CC(F)═C(C#N)C═C2C=3N═CC═NC=34 CN1CCN(CC1)C4=NC2=CC(F)═C(C#N)C═C2C=3C═CC═NC=34 N#CC=1C═C2C(═CC=1(F))N═C(C=3N═CN═CC2=3)N4CCN5CCCC5(C4) N#CC=1C═C2C(═CC=1(F))N═C(C=3N═CC═NC2=3)N4CCN5CCCC5(C4) N#CC=1C═C2C(═CC=1(F))N═C(C=3N═CC═CC2=3)N4CCN5CCCC5(C4) FC=2C═C(C═C3C=1C═NC═NC=1C(═NC=23)N4CCNCC4)C1FC=4C═C(C═C1C=4(N═C(C=2N═CC═NC1-2)N3CCNCC3))C1FC=2C═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCNCC4)C1CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C=2C═NC═NC=23))C1CN1CCN(CC1)C4=NC2=C(F)C═C(C═C2C=3N═CC═NC=34)C1CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C=2C═CC═NC=23))C1FC=2C═C(C═C3C=1C═NC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C1FC=5C═C(C═C1C=5(N═C(C=2N═CC═NC1-2)N3CCN4CCCC4(C3)))C1FC=2C═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C1FC=2C(F)═C(C═C3C=1C═NC═NC=1C(═NC=23)N4CCNCC4)C1FC=4C(F)═C(C═C1C=4(N═C(C=2N═CC═NC1-2)N3CCNCC3))C1FC=2C(F)═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCNCC4)C1CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C=2C═NC═NC=23))C1CN1CCN(CC1)C4=NC2=C(F)C(F)═C(C═C2C=3N═CC═NC=34)C1 CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C=2C═CC═NC=23))C1FC=2C(F)═C(C═C3C=1C═NC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C1FC=5C(F)═C(C═C1C=5(N═C(C=2N═CC═NC1-2)N3CCN4CCCC4(C3)))C1FC=2C(F)═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C1FC(F)(F)C1=CC═C2N═C(C=3N═CN═CC=3(C2(=C1)))N4CCNCC4FC(F)(F)C1=CC═C2N═C(C=3N═CC═NC=3(C2(=C1)))N4CCNCC4FC(F)(F)C1=CC═C2N═C(C=3N═CC═CC=3(C2(=C1)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC═C(C═C2C=3C═NC═NC=34)C(F)(F)F CN1CCN(CC1)C4=NC2=CC═C(C═C2C=3N═CC═NC=34)C(F)(F)F CN1CCN(CC1)C4=NC2=CC═C(C═C2C=3C═CC═NC=34)C(F)(F)F FC(F)(F)C1=CC═C2N═C(C=3N═CN═CC=3(C2(=C1)))N4CCN5CCCC5(C4) FC(F)(F)C1=CC═C2N═C(C=3N═CC═NC=3(C2(=C1)))N4CCN5CCCC5(C4) FC(F)(F)C1=CC═C2N═C(C=3N═CC═CC=3(C2(=C1)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C=3N═CN═CC=3(C2(=CC=1C(F)(F)F)))N4CCNCC4FC=1C═C2N═C(C=3N═CC═NC=3(C2(=CC=1C(F)(F)F)))N4CCNCC4FC=1C═C2N═C(C=3N═CC═CC=3(C2(=CC=1C(F)(F)F)))N4CCNCC4CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C=3C═NC═NC=34)C(F)(F)F CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C=3N═CC═NC=34)C(F)(F)F CN1CCN(CC1)C4=NC2=CC(F)═C(C═C2C=3C═CC═NC=34)C(F)(F)F FC=1C═C2N═C(C=3N═CN═CC=3(C2(=CC=1C(F)(F)F)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C=3N═CC═NC=3(C2(=CC=1C(F)(F)F)))N4CCN5CCCC5(C4) FC=1C═C2N═C(C=3N═CC═CC=3(C2(=CC=1C(F)(F)F)))N4CCN5CCCC5(C4) FC=2C═C(C═C3C=1C═NC═NC=1C(═NC=23)N4CCNCC4)C(F)(F)F FC=4C═C(C═C1C=4(N═C(C=2N═CC═NC1=2)N3CCNCC3))C(F)(F)F FC=2C═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCNCC4)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C=2C═NC═NC=23))C(F)(F)F CN1CCN(CC1)C4=NC2=C(F)C═C(C═C2C=3N═CC═NC=34)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C═C(C═C4(C=2C═CC═NC=23))C(F)(F)F FC=2C═C(C═C3C=1C═NC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)F FC=5C═C(C═C1C=5(N═C(C=2N═CC═NC1-2)N3CCN4CCCC4(C3)))C(F)(F)F FC=2C═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)F FC=2C(F)═C(C═C3C=1C═NC═NC=1C(═NC=23)N4CCNCC4)C(F)(F)F FC=4C(F)═C(C═C1C=4(N═C(C=2N═CC═NC1-2)N3CCNCC3))C(F)(F)F FC=2C(F)═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCNCC4)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C=2C═NC═NC=23))C(F)(F)F CN1CCN(CC1)C4=NC2=C(F)C(F)═C(C═C2C=3N═CC═NC=34)C(F)(F)F CN1CCN(CC1)C3=NC4=C(F)C(F)═C(C═C4(C=2C═CC═NC=23))C(F)(F)F FC=2C(F)═C(C═C3C=1C═NC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)F FC=5C(F)═C(C═C1C=5(N═C(C=2N═CC═NC1-2)N3CCN4CCCC4(C3)))C(F)(F)F FC=2C(F)═C(C═C3C=1C═CC═NC=1C(═NC=23)N4CCN5CCCC5(C4))C(F)(F)F FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C=3N═CN═CC2=3)N4CCNCC4FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C=3N═CC═NC2=3)N4CCNCC4FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C=3N═CC═CC2=3)N4CCNCC4CN1CCN(CC1)C4=NC2=CC(═C(C═C2C=3C═NC═NC=34)C(F)(F)F)C1CN1CCN(CC1)C4=NC2=CC(═C(C═C2C=3N═CC═NC=34)C(F)(F)F)C1CN1CCN(CC1)C4=NC2=CC(═C(C═C2C=3C═CC═NC=34)C(F)(F)F)C1FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C=3N═CN═CC2=3)N4CCN5CCCC5(C4) FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C=3N═CC═NC2=3)N4CCN5CCCC5(C4) FC(F)(F)C=1C═C2C(═CC=1C1)N═C(C=3N═CC═CC2=3)N4CCN5CCCC5(C4) CN1CCN(C(C3=NN═CN34)=NC2=C4C═C(C#N)C═C2)CC1
The activity of the compounds in Examples 1-519 as H1R and/or H4R inhibitors is illustrated in the following assay. The other compounds listed above, which have not yet been made and/or tested, are predicted to have activity in these assays as well.
The cell-based assays utilize an aequorin dependent bioluminescence signal. Doubly-transfected, stable CHO-K1 cell lines expressing human H4, or H1, mitochondrion-targeted aequorin, and (H4 only) human G protein Gα16 are obtained from Perkin-Elmer. Cells are maintained in F12 (Ham's) growth medium, containing 10% (vol./vol.) fetal bovine serum, penicillin (100 IU/mL), streptomycin (0.1 mg/mL), zeocin (0.25 mg/mL) and geneticin (0.40 mg/mL). Cell media components are from Invitrogen, Inc. One day prior to assay, the growth medium is replaced with the same, excluding zeocin and geneticin. In some assays, cells previously frozen at “ready to use density” are thawed and immediately available for loading with coelenterazine-h dye as described below.
For assay preparation, growth medium is aspirated, and cells are rinsed with calcium-free, magnesium-free phosphate-buffered saline, followed by two to three minute incubation in Versene (Invitrogen, Inc.) at 37° C. Assay medium (DMEM:F12 [50:50], phenol-red free, containing 1 mg/mL protease-free bovine serum albumin) is added to collect the released cells, which are then centrifuged. The cell pellet is re-suspended in assay medium, centrifuged once more, and re-suspended in assay medium to a final density of 5×106 cells/mL. Coelenterazine-h dye (500 μM in ethanol) is added to a final concentration of 5 μM, and mixed immediately. The conical tube containing the cells is then wrapped with foil to protect the light-sensitive dye. The cells are incubated for four hours further at room temperature (approximately 21° C.) with end-over-end rotation to keep them in suspension.
Just before assay, the dye-loaded cells are diluted to 1.5×106 cells/mL (H4 receptor) or 0.75×106 cells/mL (H1 receptor) with additional assay medium. Cells are dispensed to 1536 well micro-titer plates at 3 μL/well. To assay receptor antagonism 60 nl of 100× concentration test compounds in 100% dimethyl sulfoxide (DMSO) are dispensed to the wells, one compound per well in concentration response array by passive pin transfer, and the plates are incubated for 15 minutes at room temperature. Assay plates are then transferred to a Lumilux bioluminescence plate reader (Perkin-Elmer) equipped with an automated 1536 disposable tip pipette. The pipette dispenses 3 μL/well of agonist (histamine, at twice the final concentration, where final concentration is a previously determined EC80) in assay medium, with concurrent bioluminescence detection. Potential agonist activity of test compounds is measured by separate assays that measure response to test compounds alone, without added histamine agonist. CCD image capture on the Lumilux includes a 5 second baseline read and generally a 40 second read per plate after agonist (or test compound only in agonist mode assay) addition. A decrease in bioluminescence signal (measured either as area-under-the-curve, or maximum signal amplitude minus minimum signal amplitude) correlates with receptor antagonism in a dose dependent manner. The negative control is DMSO lacking any test compound. For antagonist assays, the positive controls are JNJ7777120 (1-[(5-Chloro-1H-indol-2-yl)carbonyl]-4-methyl-piperazine, 10 μM final concentration, H4 receptor) and diphenhydramine (2-Diphenylmethoxy-N,N-dimethylethylamine, 10 μM final concentration, H1 receptor). For agonist assays, the positive control is histamine (10 μM final concentration). Efficacy is measured as a percentage of positive control activity.
All Examples except 415, 416, and 459-62 were tested in at least an antagonist assay with an H4 positive control. Selected compounds were also tested in an H1 antagonist assay and/or in an agonist assay. In the antagonist assays, certain compounds had an EC50 of ≦10 μM, and others had an EC50 of >10 μM. In the agonist assay, certain compounds had an EC50<10 μM, others had an EC50>10 μM but <100 μM, others had no activity to 10 μM, and others had no activity to 100 μM. In certain embodiments, desirable compounds are selective H4 antagonists. In other embodiments, desirable compounds are H1/H4 antagonists.
Other compounds disclosed herein may be similarly tested as well by one of skill in the art, and it is expected that many of these compounds when tested will be active and will have utility.
Female CD-1 mice (Charles River, Hollister, Calif.), approximately 10 weeks old were housed under controlled conditions (12 h light: 12 h dark, 21° C.) and allowed ad libitum access to food (Purina LabDiet 5P14) and water. Animals were deprived of access to food and water for 1 hour during the experimental itch protocol. All studies were performed under the guidelines of the Institutional Animal Care and Use Committee of Kalypsys, Inc.
At least 24 hours prior to study initiation, the hair on the rostral dorsum of the animal was clipped to clear a location for intradermal (i.d.) injection of pruritogen (histamine, dissolved in Dulbecco's PBS [pH 7.4] at a concentration of 10 μmol per 20 μL). Animals were dosed by oral gavage with vehicle (9/0.5/0.5/90 PEG-400/Tween-80/PVP-K30/1% carboxymethylcellulose in water) or test compounds (formulated as suspensions in vehicle) at 30 mg/kg in 200 μL by means of a 20 gauge 1.5″ feeding needle affixed to a 1 mL syringe. There were 8 mice per study group. Thirty minutes after oral dosing, animals were injected i.d. with 20 μL of histamine. Immediately afterward animals were placed into individual sections of a standard acrylic cage for observation, which was recorded digitally for a 20 minute period by video cameras (Panasonic SDR-S70/PC) for later review.
Quantitation of induced itch was measured as described previously (Bell, J. K. et al., British Journal of Pharmacology, 142:374-380, 2004) by counting the number of scratching bouts per animal in the 20 minute period after i.d. injection. A scratching bout was defined as three rapid scratch movements of the hind paw in the area of the injection site. Activity with the fore paws was deemed to be grooming and not scratching, and thus was not counted. All data were analyzed using GraphPad Prism (San Diego, Calif.) software, and reported as mean percentage reduction in scratching bouts versus vehicle control. The significance of antagonist effect on agonist-induced itching was analyzed using the nonparametric Mann-Whitney test with values <0.05 being designated as statistically significant.
Certain compounds disclosed herein, when tested according to the above protocol, caused a statistically significant reduction in the number of scratching bouts (measured as % change from vehicle control) according to the criteria outlined in the protocol above. Reduction ranged from 1% to 73% over the compounds tested. Several compounds were tested on two separate days and the results taken as the mean of the two experiments. Other compounds disclosed herein may be similarly tested as well by one of skill in the art, and it is expected that many of these compounds when tested will be active and will have utility.
Male Hartley VAF outbred guinea pigs were passively sensitized to ovalbumin by a single OD subconjunctival injection of undiluted guinea pig anti-ovalbumin antiserum 24 hours before OD topical challenge with 500 μg ovalbumin in saline. Control animals were injected with saline only and challenged with ovalbumin. To determine acute phase drug efficacy, 30 min after challenge animals were clinically scored by a masked observer for severity of signs of conjunctivitis based on a standard scale. Test compounds were administered topically 1 hour prior to challenge (QD protocol), or 1 hour prior to challenge and again 8 hours after challenge (BID protocol). Twenty-four hours after challenge, animals were euthanized and conjunctivae were harvested for determination of tissue eosinophil peroxidase (EPO) concentration as a marker of allergic inflammation. Homogenates of freshly collected tissues were prepared by shaking the tissues in 2 mL round-bottom tubes containing 0.5 mL of homogenization buffer (50 mM Tris HCl, pH 8.0, 6 mM KBr) and one 5-mm stainless steel bead on a Qiagen TissueLyser at 30 Hz for 5 min. Homogenates were frozen and thawed once, then centrifuged at 10,000 rpm for 5 min. EPO activity in supernatants was measured by reacting diluted homogenates with a solution of 6 mM o-phenylenediamine substrate and 8.8 mM H2O2 in homogenization buffer for 3 min. The reaction was stopped with 4M H2SO4 and absorbances were measured at 490 nM on a spectrophotometric plate reader. Total EPO in samples was calculated from a standard curve of recombinant human EPO in each assay. EPO activity was normalized to total protein concentration (Pierce BCA assay) in supernatants. Background EPO activity was determined from the unsensitized, antigen-challenged control group. Percent inhibition was calculated from the sensitized, antigen-challenged, vehicle-treated control group in each experiment. Ovalbumin-injected animals dosed topically with 0.1% w/v dexamethasone (dex) served as positive control. Groups were compared by ANOVA with Dunnett's or Tukey's post-hoc tests where appropriate with significance assigned at the 95% confidence level.
Compounds dosed at 0.01% bid and tested in this assay were deemed to be “active” if they were statistically equivalent to dexamethasone with respect to reduction of EPO activity. Several compounds tested met this standard. “Inactive” compounds were statistically inferior to dexamethasone and not different than vehicle. Compounds dosed at ≦0.1% qd were deemed to be “active” if they were statistically equivalent to dexamethasone with respect to reduction of EPO activity; several compounds tested met this standard. “Inactive” compounds were statistically inferior to dexamethasone and not different than vehicle.
Other compounds disclosed herein may be similarly tested as well by one of skill in the art, and it is expected that many of these compounds when tested will be active and will have utility.
Female BALB/c mice, 6-12 weeks of age, were obtained from Jackson Laboratories (Bar Harbor, Me.). All experimental animals used in this work were under a protocol approved by the Institutional Animal Care and Use Committee of the National Jewish Medical and Research Center, Denver, Colo.
The assay protocol is similar to that described in Miyahara, S. et al. (2005), J Allergy Clin Immunol., 116:1020-1027. The role of the H4 receptor in this model has been validated [Shiraishi, Y. et al. (2009), J Allergy Clin Immunol., 123:S56]. Briefly, mice received intraperitoneal injections of 20 μg ovalbumin (OVA, Grade V; Sigma-Aldrich, St. Louis, Mo.), previously emulsified in 2.25 mg of alum (Alumlmuject; Pierce, Rockford, Ill.) in a total volume of 100 μL (sensitization phase). Injections occurred on days 0 and 14. Starting on day 28 onward (challenge phase), mice received daily intranasal instillation of OVA (25 mg/ml in phosphate-buffered saline), 15 μl in each nostril without anesthesia. Instillations occurred for 6 days to evoke allergic nasal inflammation and congestion. Compounds were tested for the ability to prevent induction of nasal inflammation and congestion by intranasal instillation 2.5 hours prior to OVA instillation. Instillations of compounds were performed using 10 μl (0.03 to 0.1% weight/volume [0.3 to 1 mg/ml]) in each nostril without anesthesia, in formulation vehicle: either (a) unbuffered saline, [pH approximately 6.0], 0.2% v/v Tween-80 (Sigma-Aldrich, St. Louis, Mo.), or (b) 50 mM sodium acetate [pH 5.0], 100 mM sodium chloride, 0.2% v/v Tween-80. On day 4 (early phase) and day 7 (late phase) after starting OVA challenges, respiratory frequency (RF) was measured in conscious animals by single chamber restrained whole-body plethysmography (WBP) [Buxco Research Systems, Troy, N.Y.]. Because mice are obligate nasal breathers, OVA induced nasal inflammation and congestion results in decreased breathing frequency. Compounds that block OVA-induced nasal inflammation and congestion prevent the decrease in RF compared to positive control (instillation with formulation vehicle only prior to OVA challenge). The assay negative control measures baseline RF, where challenge is performed with phosphate-buffered saline lacking OVA. Compounds were also tested without OVA challenge to demonstrate no effect on RF alone. After whole-body plethysmography on day 7, nasal airflow impedance was measured as described (RNA, see Methods section for Miyahara S. et al. [above] in the online supplemental material at the Journal of Allergy and Clinical Immunology: www.jacionline.org), using a custom-designed ventilator (Flexivent; Scireq, Montreal, Quebec, Canada). After airflow impedance measurement, the study was terminated and animals were euthanized.
Certain compounds have been tested at a concentration of 0.1% w/v in the above assay and have been found to have activitythat is statistically significant compared to positive control. Certain other compounds tested at this concentration were either weakly active, or inactive (i.e., statistically indistinguishable from positive control). One compound was tested at 0.02% w/v, and was either weakly active or inactive. Other compounds disclosed herein may be similarly tested as well by one of skill in the art, and it is expected that many of these compounds when tested will be active and will have utility.
The following are examples of compositions which may be used to orally deliver compounds disclosed herein as a capsule.
A solid form of a compound of Formula (I) may be passed through one or more sieve screens to produce a consistent particle size. Excipients, too, may be passed through a sieve. Appropriate weights of compounds, sufficient to achieve the target dosage per capsule, may be measured and added to a mixing container or apparatus, and the blend is then mixed until uniform. Blend uniformity may be done by, for example, sampling 3 points within the container (top, middle, and bottom) and testing each sample for potency. A test result of 95-105% of target, with an RSD of 5%, would be considered ideal; optionally, additional blend time may be allowed to achieve a uniform blend. Upon acceptable blend uniformity results, a measured aliquot of this stock formulation may be separated to manufacture the lower strengths. Magnesium stearate may be passed through a sieve, collected, weighed, added to the blender as a lubricant, and mixed until dispersed. The final blend is weighed and reconciled. Capsules may then be opened and blended materials flood fed into the body of the capsules using a spatula. Capsules in trays may be tamped to settle the blend in each capsule to assure uniform target fill weight, and then sealed by combining the filled bodies with the caps.
10 mg Capsule: Total fill weight of capsule is 300 mg, not including capsule weight. Target compound dosage is 10 mg per capsule, but may be adjusted to account for the weight of counterions and/or solvates if given as a salt or solvated polymorph thereof. In such a case the weight of the other excipients, typically the filler, is reduced.
20 mg Capsule: Total fill weight of capsule is 300 mg, not including capsule weight. Target compound dosage is 20 mg per capsule, but may be adjusted to account for the weight of counterions and/or solvates if given as a salt or solvated polymorph thereof. In such a case the weight of the other excipients, typically the filler, is reduced.
The following are examples of compositions which may be used to topically deliver compounds disclosed herein, for example to the eye or nasal passages.
From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.
This application is a continuation-in-part of U.S. application Ser. No. 12/556,866 filed Sep. 10, 2009, which claims the benefit of U.S. Provisional Applications No. 61/095,826, filed Sep. 10, 2008, and No. 61/231,749, filed Aug. 6, 2009, the disclosures of which are hereby incorporated by reference as if written herein in their entireties. This application also claims the benefit of U.S. Provisional Applications No. 61/312,619, filed Mar. 10, 2010 the disclosure of which is hereby incorporated by reference as if written herein in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 61312619 | Mar 2010 | US | |
| 61095826 | Sep 2008 | US | |
| 61231749 | Aug 2009 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12556866 | Sep 2009 | US |
| Child | 13044906 | US |
