OA16344A

OA16344A - Oxadiazole inhibitors of leukotriene production.

Info

Publication number: OA16344A
Application number: OA1201300100
Authority: OA
Inventors: Alessandra Bartolozzi; Todd Bosanac; Zhidong Chen; Lombaert Stéphane De; Jonathon Alan Dines; John D. Huber; Weimin Liu; Pui Leng Loke; Tina Marie Morwick; Alan Olague; Doris Riether; Heather Tye; Lifen Wu; Renee M. Zindell
Original assignee: Boehringer Ingelheim International Gmbh
Priority date: 2010-09-23
Filing date: 2011-09-20
Publication date: 2015-05-11

Abstract

The present invention relates to compounds of formula (I) and (IA) : and pharmaceutically acceptable salts thereof, wherein R1 - R5 are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.The present invention relates to compounds of formula (I) and (IA): and pharmaceutically acceptable salts thereof, wherein R1 - R5 are as defined herein. The invention also relates to pharmaceutical processes comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, for preparing these compounds and intermediates useful in these processes.

Description

This invention relates to oxadiazoles that are useful as inhibitors of five lipoxygenase activating protein (FLAP) and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the actîvity of ieukotrienes including asthma, allergy, rheumatoid arthritis, multiple sclerosis, inflammatory pain, acute chest syndrome and cardiovascular diseases including atherosclerosîs, myocardial infarction and stroke. This invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.

BACKGROUND OF THE INVENTION

Leukotrienes (LTs) and the biosynthetic pathway from arachidonîc acid leading to their production hâve been the targets of drug discovery efforts for over twenty years. LTs are produced by several cell types including neutrophils, mast cells, eosinophils, basophils monocytes and macrophages. The first committed step in the intracellular synthesis of LTs involves oxidation of arachidonîc acid by 5-lipoxygenase (5-LO) to LTA4, a process requiring the presence of the 18 kD intégral membrane protein 5-lipoxygenase-activatîng protein (FLAP) (D.K. Miller et al., Nature, 1990, 343, 278-281; R.A.F. Dixon et al., Nature, 1990, 343, 282-284). Subséquent metabolism of LTA₄ leads to LTB₄, and the cysteinyl LTs- LTC₄, LTD₄ and LTE₄ (B. Samuelsson, Science, 1983, 220, 568-575). The cysteinyl LTs hâve potent smooth muscle constricting and bronchoconstricting effects and they stimulate mucous sécrétion and vascular leakage. LTB₄ is a potent chemotactic agent for leukocytes, and stimulâtes adhesion, aggregation and enzyme release.

Much of the early drug dîscovery effort in the LT area was directed towards the treatment of allergy, asthma and other inflammatory conditions. Research efforts hâve been directed towards numerous targets in the pathway including antagonists of LTB₄ and the cysteinyl leukotrienes LTC₄, LTD₄ and LTE₄, as well as inhibitors of 5-lipoxygenase (5LO), LTA4 hydrolase and inhibitors of 5-Iipoxygenase actîvating protein (FLAP) (R.W. Friesen and D. Rîendeau, Leukotriene Biosynthesis Inhibitors, Ann. Rep. Med. Chem., 2005, 40, 199-214). Years of effort in the above areas hâve yielded a few marketed products for the treatment of asthma including a 5-LO inhibitor, zileuton, and LT antagonists, monteiukast, pranlukast and zafirlukast.

More recent work has implîcated LTs in cardiovascular disease, including myocardîal infarction, stroke and atherosclerosis (G. Riccioni et al., J. Leukoc. Biol., 2008, 13741378). FLAP and 5-LO were among the components ofthe 5-LO and LT cascade found in atherosclerotic lésions, suggesting their involvement in atherogenesis (R. Spanbroek et al., Proc. Natl. Acad. Sci. U.S.A., 2003, 100, 1238-1243). Pharmacological inhibition of FLAP has been reported to decrease atherosclerotic lésion size in animai models. In one study, oral dosing ofthe FLAP inhibitor MK.-886 to apoE/LDL-R double knockout mice fed a high-fat diet from 2 months of âge to 6 months led to a 56% decrease în plaque coverage în the aorta and a 43% decrease in the aortic root (J. Jawien et al., Eur. J. Clin. Invest., 2006, 36, 141-146). This plaque effect was coupled with a decrease in plaquemacrophage content and a concomitant increase in collagen and smooth muscle content which suggests a conversion to a more stable plaque phenotype. In another study, it was reported that administration of MK-886 via infusion to ApoE^_/_xCD4dnTpRlI mice (apoE KO mice expressing a dominant-negative TGF-beta receptor which effectively removes ail TGF-beta from the System) resulted in about a 40% decrease in plaque area în the aortic root (M. Back et al., Cire. Res., 2007, 100, 946-949). The mice were only treated for four weeks after plaque growth was already somewhat mature (12 weeks) thus raising the possibility of therapeutically treating atherosclerosis via this mechanism. In a study examining human atherosclerotic lésions, it was found that the expression of FLAP, 5-LO and LTA₄ hydrolase was significantly increased compared to healthy controls (H. Qiu et al., Proc. Natl. Acad. Sci. U.S.A., 103, 21, 8161-8166). Similar studies suggest that inhibition ofthe LT pathway, for example by inhibition of FLAP, would be useful for the treatment of atherosclerosis (for revîews, see M. Back Curr. Athero. Reports, 2008 10, 244-251 and Curr. Pharm. Des., 2009, 15, 3 i 16-3132).

In addition to the work cited above, many other studîes hâve been directed towards understandîng the biological actions of LTs and the rôle of LTs in disease. These studies hâve implicated LTs as having a possible rôle în numerous diseases or conditions (for a review, see M. Peters-Golden and W.R. Henderson, Jr., M.D., N. Engl. J. Med., 2007, 357, 1841-1854). In addition to the spécifie diseases cited above, LTs hâve been implicated as having a possible rôle in numerous allergie, pulmonary, fibrotic, inflammatory and cardiovascular diseases, as well as cancer. Inhibition of FLAP is also reported to be useful for treating rénal diseases such as diabetes-induced proteinuria (see for example J. M. Valdivieso et al., Journal of Nephrology, 2003, 16, 85-94 and A Montero et al., Journal of Nephrology, 2003, 16, 682-690).

A number of FLAP inhibitors hâve been reported in the scientific lîterature (see for example J.F. Evans et al., Trends în Pharmacological Sciences, 2008, 72-78) and in U.S. patents. Some hâve been evaluated in clinical trials for asthma, including MK.-886, MK591, and BAY XI005, also known as DG-031. More recently, the FLAP inhibitor AM103 (J.H. Hutchînson et al., J. Med. Chem. 52, 5803-5815) has been evaluated in clinical trials, based on its anti-inflammatory properties (D.S. Lorrain et al., J. Pharm. Exp. Ther., 2009, DOL10.1124/jpet. 109.158089). Subsequently, it was replaced by the back-up compound AM-803 (GSK-2190915) for the treatment of respiratory diseases. DG-031 has also been in clinical trials to evaluate its effect on biomarkers for myocardial infarction risk and showed a dose-dependent suppression of several biomarkers for the disease (H. Hakonarson et al., JAMA, 2005, 293, 2245-2256). MK.-591 was shown in a clinical trial to reduce proteinuria in human glomerulonephritis (see for example A. Guash et al., Kidney International, 1999, 56, 291-267).

However, to date, no FLAP inhibitor has been approved as a marketed drug.

BRIEF SUMMARY OF THE INVENTION

The présent invention provides novel compounds which inhibît 5-lipoxygenase activatîng protein (FLAP) and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the activity of leukotrienes, including allergie, pulmonary, fibrotic, inflammatory and cardiovascular diseases and cancer. This invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.

DETAILED DESCRIPTION OF THE INVENTION

In its first broadest embodiment, the présent invention relates to a compound of formula

I:

wherein:

R¹ and R² together with the carbon atom to which they are attached form a C₃_iq carbocyclic ring or a 5-11 membered heterocyclic ring, wherein each carbocycle or heterocycle îs optionally independently substituted with one to two groups selected from Ci-6 alkyl and halogen;

R³ îs 5-11 membered heteroaryl ring containing one to three heteroatoms selected from nitrogen, oxygen and sulfur, wherein each R is optionally independently substituted with one to three groups selected from Cm alkyl, Cm alkoxy, Cm alkylhydroxy, -CN, amino, Cm alkylamîno and Cm dialkylamino; νΛ

R⁴ is hydrogen, halogen, Cm alkyl or nitrile;

R⁵ is Ci-6 alkyl, C₃.jo carbocycle, 5-l l membered heterocycle, aryl, 5-11 membered heteroaryl, -C(O)-R⁶ or -NR⁷R^K, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R¹

R⁶ is C₃.₈ heterocycle, amino, Ci_₃ alkylamino, Ci.₃ dialkylamino or -NH-5-6 membered heterocycle, each optionally independently substituted with one to three groups selected from R⁹, R^t0 and R¹¹;

R and R are each independently hydrogen, -S(O)_nCi_6alkyl or Cm alkyl;

R⁹, R¹⁰ and R¹¹ are independently selected from (a)-H, (b)-OH, (c) halogen, (d)-CN, (e)-CF (f) C].6alkyl optionally substituted with one to three -OH, -N(R^l2)(R¹³) , aryl, -O-C|.₂alkyl-aryl, 3-6 membered heterocycle, -C(O)- 3-6 membered heterocycle, C|.<,aikoxy , -S(O)_nCMalkyl, -CO₂R¹², halogen, -CN or -C(O)N(R^,2)(R'³), (g) Ci.₆alkoxy, (h) -N(R¹²)(R¹³), (i) -S(O)_nCi.₆alkyl, (j) -€O₂R¹², (k) -C(O)N(R^,2)(R¹³), (l) -S(O)₂N(R¹²)(R^lî), (m) a 3-10 membered heterocyclic group optionally substituted with one to three groups selected from -OH, Cm alkyl, Cj.6alkylhydroxy, Ci_₆alkyl-CO'R¹², -S(O)nC|. «alkyl, oxo, -C(O)N(R^I2)(R¹³), and -CO2R¹², (n’) oxo, (o) -C(0)-C|.3 alkyl, (p) -C(O)-3-6 membered heterocycle optionally substituted with one to three groups selected from halogen hydroxy and C|.t,alkoxy, (q) -OR¹², (r) 5-11 membered heteroaryl;

R¹² and R¹³ are each independently selected from -H, -C(.6alkyl, -C(O)-C|_6 alkyl, Cj.io carbocycle and a 3-6 membered heterocyclic group, each of which is optionally independently substituted with one to three -OH, Ci.6 alkyl, Ci-ôalkoxy, C(O)N(R^l4)(R¹⁵), -S(O)BC_Malkyl, CN, C₃.₁₀ carbocycle, -CO₂R¹⁴, CF₃,3-6 membered heterocycle,halogen; or i 3

R and R together with the nitrogen atom to which they are attached form a heterocyclyl ring optionally substituted with one to three -OH, CN, Ci.6alkoxy or oxo;

R¹⁴ and R^li are each independently selected from -H and -Cj^alkyl;

n is 0, 1 or 2;

or a pharmaceutically acceptable sait thereof.

In a second embodiment, the présent invention relates to a cornpound as described in the broadest embodiment above, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, 2.2.1 bicycloheptyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidînyl, tetrahydrothienyl, wherein each carbocycle or heterocycle is optionally independently substituted with one to two groups selected from Cj.6 alkyl and halogen;

R³ îs pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, imidazolyl, thienyl, furanyl or thiazolyl, wherein each R³ is optionally independently substituted with one to three groups selected from C1-3 alkyl, Ci.3 alkoxy, C|_₃ alkylhydroxy, -CN, amino, Cj.₃alkylamino and C]_₃ dialkylamino;

R⁴ is hydrogen, halogen or methyl;

R⁵ is methyl, ethyl, propyl, isopropyl, butyl, îsobutyl, tert. butyl, pentyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, phenyl, piperidinyl, pîperazinyl, morpholinyl, thiomorpholinyl, pyrrolidinyl, tetrahydropyranyl, pyrrolyl, thienyl, furanyl, thiazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, triazolyl, dihydropyridinyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quinolinyl, isoquinolinyl, indolyl, pyrrolopyridinyl, pyrrolopyrimidinyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, -C(O)-R⁶, hydroxy or NR⁷R\ wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R¹¹;

R⁶ is azetidinyl, pyrrolidinyl, piperidinyl, pîperazinyl, tetrahydropyranyl, morpholinyl, thiomorpholinyl, amino, C_t.₃ alkylamino, C].₃ dialkylamino or-NH-5-6 membered heterocycle, each optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R^u;

R⁷and R⁸ are each independently hydrogen, C1.5 alkyl or -S(O)_nCi__ftalkyl;

R⁹, R¹⁰ and R¹¹ are independently selected from (a)-H, (b)-OH, (c) halogen, (d)-CN, (e)-CF (f) Ci-^alkyl optionally substituted with one to three -OH, -N(R^,3)(R¹³) , phenyl, benzyl, phenethyl, azetidinyl, pyrrolidinyl, piperidinyl, pîperazinyl, morpholinyl,

C(O)- 3-6 membered heterocycle, C ^alkoxy, -S(O)_nCi.₆alkyl, -CO₂R¹², halogen, CN or -C(O)N(R^I2)(R¹³), (g) Ci.₆alkoxy, (h) -N(R^]2)(R¹³), (i) -S(O)_tlC_l.₆alkyl, (j) CO₂R¹², (k) -C(O)N(R^,2)(R¹³), (l) -S(O)₂N(Rⁱ²)(R¹³), (m) oxetanyl, tetrahydrofuranyi, tetrahydropyranyl, azetidinyl, pyrrolidinyl, tetrahydrothienyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl or thiomorpholinyldioxide, optionally substituted with one to three groups selected from -OH, Ci-6alkyl, Ci.₆ alkylhydroxy, Cj.6 alkyl-CO₂R¹², -S(O)_nC|.6alkyl, oxo, C(O)N(R^l2)(R¹³), and COjY.

(n’) oxo, (o) -C(O)-Cj_₃ alkyl, (p) -C(O)-3-6 membered heterocycle optionally substituted with one to three groups selected from halogen hydroxy and C|.₆alkoxy, (q) -OR¹², (r) imidazolyl, pyrrolyl, pyrazolyl, thienyl or furanyl;

R¹² and R¹³ are each independently selected from -H, -Ci^alkyl, -C(O)-Ci-6 alkyl, cyclopropyl, cyclobutyl, cyclopentyl and a 3-6 membered heterocyclic group, each of which is optionally independently substituted with one to three -OH, Ci-e alkyl, Ci. 6alkoxy, -C(O)N(R¹⁴)(R¹⁵), -S(O)nCK₆aikyl, CN, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, -CO₂R¹⁴, CF₃, 3-6 membered heterocycle, halogen; or

R¹² and R¹³ together with the nitrogen atom to which they are attached form a heterocyclyl ring optionally substituted with one to three -OH, CN, C].6alkoxy or oxo;

R¹⁴ and R^1S are each independently selected from -H and —Cj.₆alkyl;

n is 0 or 2; à/'' or a pharmaceutically acceptable sait thereof.

In a third embodiment, the présent invention relates to a compound as described in any of the preceding embodiments above, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl, cyclopentyl cyclohexyl, or tetrahydropyranyl wherein each carbocycle or heterocycle is optionally independently substituted with one to two groups selected from Cj.₃ alkyl and halogen;

or a pharmaceutically acceptable sait thereof.

In a fourth embodiment there îs provided a compound of formula (I) as described in any of the preceding embodiments above, wherein:

R is pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl, wherein each R is optionally independently substituted with one to three groups selected from C|.₃ alkyl, Cm alkoxy, Ci-3 alkylhydroxy, -CN, amino, Cm alkylamino and Cm dialkylamino;

or a pharmaceutically acceptable sait thereof.

In a fifth embodiment there is provided a compound as described in any of the preceding embodiments above, wherein:

R⁵ is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert. butyl, pentyl, hexyl, phenyl, piperidinyl, piperazînyl, morpholinyl, thiomorpholinyl, pyrrolidinyl, furanyl, thîazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, triazolyl, dihydropyridinyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quînolinyl, isoquinolinyl, indolyl, pyrrolopyridinyl, pyrrolopyrimidinyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, -C(O)-R⁶, hydroxy or-NR⁷R⁸, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R¹¹;

R⁶ is azetidinyl, pyrrolidinyl, piperidînyl, piperazinyl, morpholinyl, amino, C(.₃ alkylamino or Cm dialkylamino;

R⁷and R⁸ are each independently hydrogen, C].₅ alkyl or -S(O)₂Ci_₆alkyl;

R⁹,Rⁱ⁰ andR are independently selected from (a)-H, (b)-OH, (c) halogen, (d)-CN, (e)-CF (f) Ci.₆alkyl optionally substituted with one to three -OH, -N(R¹²)(R^I3) , phenyl, benzyl, phenethyl, azetidinyl, pyrrolidinyl, piperidînyl, piperazinyl, morpholinyl, C(O)- 3-6 membered heterocycle, C|.₆alkoxy, -S(O)_nC].₆alkyl, -CO₂R¹², halogen, CN or -C(O)N(R¹²)(R¹³), (g) Ci_₆alkoxy, (h) -N(R¹²)(R¹³), (i) -S(O)₂C].₆alkyl, (j) -CO₂R¹², (k) -C(O)N(R^l2)(R^!3), (l) -S(O)₂N(R^l2)(R¹³), (m) oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, tetrahydrothîenyl, azetidinyl, pyrrolidinyl, piperidînyl, piperazinyl, morpholinyl, thiomorpholinyl or thiomorpholinyldioxide, optionally substituted with one to three groups selected from -OH, C_t_6alkyl, Ci_6alkylhydroxy, C].6alkyl-CO₂R¹², -S(O)_nCi_6alkyl, oxo, C(O)N(R¹²)(R¹³), and-COiR¹², (n’) oxo, (o) -C(O)-C|_3 alkyl, (p) -C(O)-3-6 membered heterocycle optionally substituted with one to three groups selected from halogen hydroxy and Ci_6alkoxy, (q) -OR¹², (r) imidazolyl, pyrrolyl, pyrazolyl, thienyl or furanyl;

R¹² and R¹³ are each independently selected from -H, -Cj^alkyl, -C(O)-C|.6 alkyl, cyclopropyl, cyclobutyl, cyclopentyl and a 3-6 membered heterocyclic group, each of which is optionally independently substituted with one to three -OH, Ci^ alkyl, C]. 6alkoxy, -C(O)N(R^l4)(R¹⁵), -S(O)nCi_₆alkyl, CN, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, -CO2R¹⁴, CF3, 3-6 membered heterocycle, halogen; or

R and R together with the nitrogen atom to which they are attached form a heterocyclyl ring optionally substituted with one to three -OH, CN, Ci »,alkoxy or oxo;

R¹⁴ and R¹⁵ are each independently selected from -H and -C|._ôalkyl;

n = 2;

or a pharmaceutically accepted sait thereof.

In a sixth embodiment there is provided a compound of formula (I) as described in the first or second embodiment above, wherein:

O

R and R together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl each optionally independently substituted with one to two groups selected from methyl and fluoro;

R³ is pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl, wherein each R³ îs optionally independently substituted with one to three groups selected from methyl, -CN, -NH-CH3 and an amino group;

R⁴ is hydrogen;

R⁵ îs phenyl, piperidinyl, piperazinyl, pyrrolidinyl, thiazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, triazolyl, dihydropyridinyl, pyridinyl, pyrimidinyl, pyrazinyl, ^/ pyridazinyl, pyrazolopyrimidinyl, îmidazopyridinyl, indazolyl, or -NR⁷R⁸, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰and R¹¹;

R and R are each independently hydrogen or C 1.3 alkyl ;

R⁹, R¹⁰ and R¹¹ are independently selected from (a)-H, (b)-OH, (c) halogen, (d)-CN, (e) -CFj, (i) Ci.₆alkyl optionally substituted with one to three -OH, -N(R^,2)(R¹³), phenyl, benzyl, phenethyl, azetidînyl, pyrrolîdinyl, piperidinyl, piperazînyl, morpholinyl, C(O)- 3-6 membered heterocycle, Ci.₆alkoxy, -S(O)2Cj_₆alkyl, -CO2R¹², halogen, CN or -C(O)N(R^l2)(R¹³), (g) Ci.₆alkoxy, (h) -N(R^l2)(R¹³), (i) -S(O)₂C,.₆alkyl,

G)^CO₂R¹², (k) -C(O)N(R^]2)(R^lî), (l) -S(O)₂N(R¹²)(R¹³), (m) oxetanyl, tetrahydrothienyl, pyrrolîdinyl, piperidinyl, piperazînyl, morpholinyl, thiomorpholinyl or thiomorpholinyldioxide, optionally substituted with one to three groups selected from -OH, Cj 4 alkyl, Ci.₆alkylhydroxy, C]_₆alkyl-CO₂R¹², -S(O)2Ci. 6alkyl, oxo, -C(O)N(R^l2)(R¹³), and -CO2R¹², (n’) oxo, (o) -C(O)-C,.₃ alkyl, (p) -C(O)-piperidinyl or^C(O)-pyrrolidinyl each optionally substituted with one to three groups selected from halogen hydroxy and C].₆alkoxy, (q) -OR¹², (r) imidazolyl, pyrrolyl or pyrazolyl;

R¹² and R¹³ are each independently selected from -H, -Ci_6alkyl, C(O)-C|.b alkyl, cyclopropyl, cyclobutyl, cyclopentyl and a 3-6 membered heterocyclic group, each of which is optionally independently substituted with one to three -OH, Ci^ alkyl, Ci. ^alkoxy, -C(O)N(R¹⁴)(R¹⁵), -S(O)2Cj.6alkyl, CN, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, -CO2R¹⁴, CF3,3-6 membered heterocycle, halogen; or

R¹² and R¹³ together with the nitrogen atom to which they are attached form a heterocyclyl ring optionally substituted with one to three -OH, CN, Ci.₆alkoxy or oxo;

R¹⁴ and R¹⁵ are each independently selected from -H and -Cj^alkyl;

or a pharmaceutically accepted sait thereof.

In a seventh embodiment there is provided a compound as described in the embodiment above, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl; or a pharmaceutically acceptable sait thereof.

In an eighth embodiment there is provided a compound as described in the sixth embodiment above, wherein:

R¹ and R² together with the carbon atom to which they are attached is tetrahydropyranyl; or a pharmaceutically acceptable sait thereof.

In a ninth embodiment there is provided a compound as described in the sixth embodiment above, wherein:

R³ is selected from

or a pharmaceutically acceptable sait thereof.

In a tenth embodîment there is provided a compound as described in the sixth embodîment above, wherein:

R⁵ is selected from imidazolyl, pyrazolyl, triazolyl, thiazolyl, oxazolyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, dihydropyridinyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolidinyl, and phenyl, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R^u;

or a pharmaceutically acceptable sait thereof.

In an eleventh embodîment there is provided a compound as described in the sixth embodîment above, wherein:

7 8 9 10

R Îs-NR R , optionally substituted with oneto three groups selected from R , R and R¹¹;

or a pharmaceutically acceptable sait thereof.

In a twelfth embodîment there is provided a compound as described in the sixth embodîment above, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl ;

R³ is selected from

R⁴ is hydrogen;

R⁵ îs selected from imidazolyl, pyrazolyl, triazolyl, thiazolyl, oxazolyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolidinyl, and phenyl, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R^l° and R^u;

or a pharmaceutically acceptable sait thereof.

In a thirteenth embodiment there îs provided a compound as described in the sixth embodiment above, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl;

R³ is selected from

H J and II h₂n^^n

R⁴ is hydrogen ;

7 8* ♦ 9 10

R is -NR R optionally substituted with one to three groups selected from R , R and

or a pharmaceutically acceptable sait thereof.

In another first broadest embodiment, the présent invention relates to a compound of formula IA: y/'

ΙΑ wherein:

l 2

R and R together with the carbon atom to which they are attached form a C₃._lucarbocyclîc ring or a 5-l l membered heterocyclic ring, wherein each carbocycle or heterocycle îs optionally independently substituted with one to two groups selected from Ci-6 alkyl and halogen;

R is 5-11 membered heteroaryl ring contaîning one to three heteroatoms selected from nitrogen, oxygen and sulfur, wherein each R³is optionally independently substituted with one to three amino groups;

R⁴ is hydrogen, Cj.₃ alkyl or halogen;

R⁵ is 5-l l membered heteroaryl optionally independently substituted with one to three Ci_6 alkyl groups;

or a pharmaceutically acceptable sait thereof.

In a second embodiment, the présent invention relates to a compound of formula (IA) as described in the broadest embodiment above, wherein:

R and R together with the carbon atom to which they are attached is cyclopropyl, cyclobutyl, cyclopentyl, tetrahydrofuranyl, tetrahydropyranyl, wherein each carbocycle or heterocycle is optionally independently substituted with one to two groups selected from C|.6 alkyl and halogen;

R³ is pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, wherein each R³ is optionally independently substituted with one to three amino groups;

R⁴ is hydrogen;

R⁵ is pyrrolyl, thienyl, furanyl, thîazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, triazolyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quinolinyl, isoquinolinyl, indolyl, pyrrolopyridinyl, pyrrolopyrimidinyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, wherein each R⁵ is optionally substituted with one to three Cj._(l alkyl groups; or a pharmaceutically acceptable sait thereof.

In a third embodiment, the présent invention relates to a compound of formula (IA) as described in any of the preceding embodiments above, wherein:

R and R together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl;

or a pharmaceutically acceptable sait thereof.

In a fourth embodiment there is provided a compound of formula (IA) as described in any of the preceding embodiments above, wherein:

R³ is pyrimidinyl substituted with an amino group; or a pharmaceutically acceptable sait thereof.

In a fifth embodiment there îs provided a compound of formula (IA) as described in any of the preceding embodiments above, wherein:

R⁵ is pyrazolyl or, pyridinyl, each optionally substituted with one to three C|.j alkyl groups;

or a pharmaceutically acceptable sait thereof.

ln a sixth embodiment there is provided a compound of formula (IA) as described in the second embodiment above, wherein:

I 9

R³ is pyrimidinyl substituted with an amino group;

R⁴ is H

R⁵ is pyrazolyl or, pyridinyl, each optionally substituted with one to three methyl groups; or a pharmaceutically acceptable sait thereof.

The following are représentative compounds of the invention which can be made by the general synthetic schemes, the examples, and known methods in the art.

Table I

Example	Structure	Name
i	A J N	tert-butyl 4-[5-(3-{l -[6(2-aminopyrimidin-5yl)pyridin-3yl]cyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-yl]piperazine-1carboxylate
2	Άι ^{N h}=ⁿ h₂n n' °	A-2-[5-(3-{1-(6-(2- aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridin-

		2-yl]glycinamîde
3	A» VApC^NHn^A? ^Ν'° η₂νΑ	5-(5-(1-(5-(6- (piperazin-1 -yl)pyridin3-yl]-1,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
4	rAvr^ _Νγ-Μ N-_Oy-- A J η₂ν ν	5-(5- {1 - [ 5-( 1 H-pyrazol3-yl)-l,2,4-oxadiazol-3yl]cyclobutyl} pyridin-2yl)pyrimidin-2-amine
5	Γ^ν-Ο ν^Αα ^ν'° Λ J η₂ν ν	5-(5-( 1-(5-(3methylphenyl)-1,2,4oxadiazol-3yl Jcyclobutyl} pyrîdin-2 yl)pyrimidin-2-amine
6	yAo-- νΧν ⁰ A J η₂ν ν	5-(5-(1-(5-(4- methylphenyl)-1,2,4oxadîazol-3yljcyclobutyl} pyridin-2yl)pyrimidÎn-2-amine
7	rAv-Or ν AV ^Ν° ⁰ Λ 3 η₂ν ν	5-(5-(1-(5-(4- (rnethylsulfonyl)phenyl] -l,2,4-oxadiazol-3yl}cyclobutyl)pyridîn-2yl]pyrimidin-2-amine
8	AVa ν'Υν ^ο / Λ J η₂ν ν	5-(5-(1-(5-(6(ethyl amino)pyridin-3 yl]-l,2,4-oxadiazol-3y 1} cyclobutyl )pyridin-2yl]pyrimidin-2-amine

9	JX _N H ^Nv n A' N ⁰ D> aJ h₂n n	5-[5-(l-{5-[6- (cyclopropylamino)pyri din-3-yl]-l,2,4oxadiazol-3yl} cyclobut yl)pyridin-2yl]pyrimidin-2-amine
ΙΟ	X/ NH, _L Jl S-c/ n-nh n-yn ^u A J h₂n n	5-(5-{l-[5-(5-amino- l H-pyrazol-3-yl)-1,2,4oxadîazol-3yl]cyclobutyl}pyridîn-2yl)pyrimidin-2-amine
11	n^v-Q ^N o '/ X 2 o \ h₂n n	5-[5-(l-{5-[3(methylsulfonyl)phenyl] -l,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
12	Ai ^ho7\ h₂n n	l-{[5-(3-[l-[6-(2- aminopyrimidin-5yl)pyridin-3yl]cyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-yl]amino}-2methyipropan-2-ol
13	Υχ ^N of h₂n n °	ethyl 7V-[5-(3-{ l-[6-(2aminopyri midin-5 yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-yl]glycînate

14	nAJ ⁿ~° ⁿ ^N Λ J h₂n n	5-(5-{l-[5-(lH-l,2,3triazol-4-yl)-l,2,4oxadiazol-3yl]cyclobutyl}pyridin-2- yl)pyrimidin-2-aniine
15	aaJAC-N / il J N-o ^X N N ^u A J H₂N N	5-(5-(1-(5(dimethylamino)-1,2,4oxadiazol-3yljcyclobutyl} pyridin-2yl)pyrimidîn-2-amine
16	^Α>Χν Λ^ν\_Η _XTI_o>AJa TA^N ° _HCA h/AA ⁰	7/-(5-(3-(1-(6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-yl]glycine
17	r^y-Or™²nAJ -A ⁰Λ J h₂n n	4-(3-(1-(6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5yl)benzenesulfonamide
18	,α-,Λ-ν /=^N\_ h fjI₀A7A A J ^{N HO}i h₂n n	1-(((5-(3-(1-(6-(2amînopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2yl]amino} methyl )cyclop ropanol

A

19	NH, /\ °'S-~ AX Λ 2 h₂n n	3-(3-{l-[6-(2- aminopyrimidin-5yl)pyridin-3yl]cyclobutyl} -1,2,4oxadiazol-5yl)benzenesulfonamide
20	nVn^{j ν}'ο\?^ν H₂N N F F	5-[5-(l-{5-[l-methyl-3- (trifluoromethyl)-1Hpyrazol-4-yl]-1,2,4oxadiazol-3yl} cyclobutyl)pyridin-2yl]pyrimidin-2-amine
21	^i\Y\^N /=N h x j y ύυυ ^N'° HO^ h₂n^Y	2-{[5-(3-{ 1-(6-(2- aminopyriniidin-5yl)pyridin-3yljcyclobutyl] -1,2,4oxadiazol-5-yl)pyridin2-yl]amino}-2methylpropan-1 -ol
22	ί^Ί\| if^N)— _NyA/ J A J ^H0 h₂n n	2-{[5-(3-( 1-(6-(2- aminopyrimidin-5yl)pyridin-3yl]cyclobutyl}-l,2,4oxadîazoi-5-yl)pyridin- 2-yljoxy} éthanol
23	N^''' Y ^νό N Λ J h₂n n	5-(5-( 1-(5-( 1,3-thiazol- 4-yl)~ 1,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine

24	pXjA./° JL J N-rj ^kΝ' Ν ηρ Ν ^U Λ J h₂n n	5-(5-{l-[5-(l,3-oxazol- 4-yl)-1,2,4-oxadiazol-3yl]cyclobutyl] pyridin-2yl)pyrimidin-2-amine
25	jfjj Hi _NxJ/ ^N'O Y > A J HjN N	5-(5-{ l-[5- (pyrazolo[l,5a]pyrimidin-3-yl)-1,2,4oxadiazol-3yl]cyclobutyl} pyridin-2yl)pyrimidin-2-amine
26	h₂n^n'	5-(3-{l-[6-(2aminopyrimidin-5yl)pyridin-3yl]cyclobutyl} -1,2,4oxadiazol-5-yl)-lmethylpyridin-2( 1H)one
27	XJn- j N '^:- N ^u Λ J H_:N N	5-(5-{l-[5-(imidazo[l,2a]pyridin-6-yl)-1,2,4oxadîazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
28	/\ ^0. aXa /Ύ jf Y X W nYX ^N~° h/Y	5-[5-(l-{5-[l-(2- methoxyethyl)-1Hpyrazol-4-yl]-1,2,4oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine

29	O X^0H f T S aU n'V'A^ ⁿ'° A J h₂n n	2-(4-(3-(1-(6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)- i Hpyrazol-1 -yljpropan-1 ol
30	o jc°^H xuïA-n A J h₂n n	2-(4-(3-(1-(6-(2- aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)-1Hpyrazol-l-yl]-2methylpropan-1 -ol
31	ΓΛ^νΑ>Αν n'XV ^N-o ^K=N A J Η₂Ν N	5-(5-(1-(5-(6-( 1Himidazol-1 -yl)pyridin-3yl]-l,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
32	fnMA .A fi N-o N Y N ^u A J h₂n n	4-(3-( 1-(6-(2- aminopyrimidin-5yl)pyridin-3yljcyclobutyl}-1,2,4oxadiazol-5-yl)phenol
33	N > N ⁰ _Hn_/ A J h₂n n	2-((5-(3-(1-(6-(2- aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-yl] amino (propane1,3-diol

34	η,ν^Λν^ ⁰ _; ^N	l-[5-(3-{l-[6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-yl ]-M7V-d imethyl-Lprolinamide
35	Ν Υ Ν ⁰ 1 ° °^H	1- [5-(3-{l-[6-(2- aminopyrimidin-5yl)pyridin-3yljcyclobutyl}-1,2,4oxadiazol-5-yl)pyridin- 2- yl]-L-proline
36		methyl 1-(5-(3-( l-[6-(2aminopyrimidin-5yl)pyridîn-3yl]cyclobutyl] -1,2,4oxadiazol-5-yl)pyridin2-yl]-L-prolinate
37	mvi Ai J N-o N'^N N N ^υ A J h₂n n	5-(5-{l-[5-(4-methyl- 4H-l,2,4-triazol-3-yl)- l,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
38	^τΛ:α>ο^η N -'·- N ⁰ „ i J! J °^ H/Ttl f	methyl (2Æ)-l-[5-(3-{l- [6-(2-aminopyrimidin-5yl)pyridin-3yl]cyclobutyl} -1,2,4oxadiazol-5-yl)pyridîn2-yl]piperazine-2carboxylate

39	ïV^{n N}'° H χ Α ⁰	methyl (25)-4-(5-(3-( l[6-(2-aminopyrimidin-5yl)pyridin-3yl]cyclobutyl}-1,2,4oxadiazol-5-yl)pyridin2-yl]piperazine-2carboxylate
40	f’fl* v<AO^h nAXi ^N~° Y-0 A J o^{r x} HjN N	methyl (2λ)-4-[5-(3-{1 - [6-(2-aminopyrimidin-5yl)pyridin-3yljcyclobutyl )-1,2,4oxadiazol-5-yl)pyridin2-yl]piperazine-2carboxylate
41	nSvCrO^H ⁰ ^OH η₂ν^ΛΑ ⁰	(25)-4-(5-(3-(1-(6-(2aminopyrimidin-5yl)pyridin-3- yl (cyclobutyl) -1,2,4oxadiazol-5-yl)pyridin2-yl]piperazine-2carboxylic acid
42	ⁿ ° y oh η₂ν^ΛΑ ⁰	(2R)-4-[5-(3-(1-(6-(2aminopyrimidin-5yl)pyridin-3yl (cyclobutyl) -1,2,4oxadiazol-5-yl)pyridin2-yl]piperazine-2carboxylic acid

43	•.A·,^{1 Ν}-° η₂ν^'ν'	(37?)-1-(5-(3-{1-(6-(2aminopyriinidin-5yl)pyridin-3yljcyclobutyl} - i ,2,4oxadiazol-5-yl)pyridin2-yl]pyrrolidin-3-ol
44	_z<xJX.,n Α\ Η ïj ^{Ν ηο}\	(2/?)-1-((5-(3-{1-(6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadîazol-5-yl)pyridin2-yl]amino}propan-2-ol
45	ναΛγ ^ν'° ( A J oh h₂n n	{(22?)-1-(5-(3-( 1-(6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridîn2-yl]pyrrolidin-2yl} methanol
46	AÛÛT-cHZH 7 ^N HO^-/ h₂n^A	(2S)-1-((5-(3-{1-(6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyrîdîn2-yl]amino}propan-2-ol
47	αΛ^νηαΟ~μ A J h₂n n	ethyl 3-{4-(5-(3-{1-[6(2-aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol -5 -yl)pyridin2-yl]piperazin-l-

		yl}propanoatc
48	^N O h₂n'^'n^	(3S)-l-[5-(3-{ l-[6-(2aminopyrimidin-5yl)pyrîdin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-yl]pyrrolidin-3-ol
49	ΐΡΥγ^N z V^{- N}CZ/^S' o n^vM N-cO^^{7 0} Λ J h₂n n	5-[5-(l-(5-[6-(l,ldioxidothiomorpholin-4yl)pyridin-3-yl]-l,2,4oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
50	ί Ύ Ύ r\j n^An^ ^N-° Λ 3 h₂n n	5-{5-[l-(5-{6-[4(methylsu lfonyl )piperazi n-l-yl]pyridin-3-yl}l,2,4-oxadiazol-3yl)cyclobutyl]pyridin-2yl} pyriinidin-2-amine
51	J n-0^ ^=^9 ) N N ^u -S' η₂Λ^ o	5-(5-( l-[5-(6-{[2(methylsulfonyl)ethylja mîno}pyridin-3-yl)l,2,4-oxadîazol-3yljcyclobutyl} pyridin-2yl)pyrimidin-2-amine
52	O 0 Λ J h₂n n	5-{5-[l-(5-{6-[3- (methyisulfonyl)pyrrolid in-l-yl]pyridin-3-yl}l,2,4-oxadiazol-3yl)cyclobutyl]pyridin-2yi! pyrimidin-2-amine

53	OH fil \|T —Ç /)—N ⁰ _EV«^J A 7 h₂n n	3-{4-[5-(3-{ l-[6-(2aminopyrimidin-5yl)pyridîn-3yl]cyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-yl]piperazin-lyl}propanoic acid
54	^ΑΎν-.ϊ^'-Χ,η N A' N ^OH H₂N^A	l-[4-(3-{l-[6-(2aminopyrimidin-5yl)pyridîn-3yljcyclobutyl} -1,2,4oxadiazol-5-yi)-l H- pyrazol-l-yl]-2methylpropan-2-ol
55	/'ÂyA /^n n-AÎ^-^a h₂AA	5-[5-( l - {5-[ l-(oxetan-3yl)-1 H-pyrazol-4-yl]l,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
56	ZX A N-n Ν 'V N ⁰ 0- A J H₂N N	5-{5-[l-(5-{5-[(2methoxyethyl)amino]py razin-2-yl}-1,2,4oxadiazol-3yl)cyclobutyl]pyridin-2yl}pyrimidin-2-ainine
57	CjsⁿAAA nAV ⁿ-° ⁿ A J h₂n n	5-[5-(l-{5-[5- (ethylamino)pyrazin-2yl]-l,2,4-oxadiazol-3yl]cyclobutyl)pyridin-2yl]pyrimidin-2-amine

58	/==n hn' X JX ⁰ ° A fi H₂N N	2-[4-(3-{l-[6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)-lHpyrazoi-l-ylJWmethylacetamide
59	Λ-A ,N /=?N 0	2-[4-(3-{l-[6-(2- aminopyrimidin-5yl)pyridîn-3yl]cyclobutyl}-l,2,4oxadîazol-5-yl)-1Hpyrazol-1-yiJ-jVWdimethylacetamide
60	πΛμΎΟπ n^zSA ⁿ-° ⁿ A fi h₂n n	5-[5-(l-{5-[5- (piperazin- i -yl)pyrazîn2-yl]-l ,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
61	fÂUlO' Ν-γΜ ^N~° ^N A fi h₂n n	5-[5-(l-{5-[5-(4methylpiperazin-1 yl)pyrazin-2-yl]-1,2,4oxadiazol-3yl} cyclobutyl)pyridin-2yl]pyrimidin-2-amine
62	ΑΖ^νΑ>Α^νη /χ Ζ fi N-o N Z n ^U A fi h₂n n	5-[5-(l-{5-[4- (piperazin-1 -yl)phenyl]l,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine

63	aA^AA n A^ n ⁰ A J h₂n n	5-(5-{ l-[5-(l -ethyl-1Hpyrazol-4-yl)-1,2,4oxadiazol-3yljcyclobutyl} pyridin-2yl)pyrimidin-2-amine
64	^Υγ N /¾ N -A J LcPV A J ' h₂n n	5-[5-( 1 -{5-[ 1 -(propan-2yl)-1 H-pyrazol-4-yl]- 1,2,4-oxadîazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
65	yA^An AN a y lh-nj nAn ⁰ A h₂n'^'n' ^{0 0H}	2-[4-(3-{l-[6-(2aminopyrimidin-5yl)pyridin-3yl]cyclobutyl} -1,2,4oxadiazol-5-yl)-1Hpyrazol-l-yl]-2methylpropanoic acid
66	Y^yA-n an J n^Af N A N ^u [ A J F h₂n n	5-[5-(l-{5-[l(difluoromethyl)-l Hpyrazol-4-yl]-1,2,4oxadiazol-3yl}cyclobutyI)pyridin-2yl]pyrimidin-2-amine
67	^'A/N, an ,,A^JA<s A 0 h₂n n	5-[5-(l-{5-[l-(2fluoroethyl)-lHpyrazol-4-yl]-1,2,4oxadiazol-3yl} cyclobutyl )pyridin-2yl]pyrimidin-2-amine

68	Α\Λ /^n _f I N N ^υ F Λ J h₂n n	5-[5-( l-{5-[ 1-(2,2difluoroethyl)-1Hpyrazol-4-yl]-l,2,4oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
69	<+\Xa. /^N F AUîKn U N N ^u F A J H,N N	5-[5-( l-{5-[ 1-(2,2,2- trifluoroethyl)-lHpyrazol-4-yi]-1,2,4oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
70	AA-. N ΛΝ jf J jf Avn. ⁰ 1 A A o' 'nh₂ h₂n n ²	2-[4-(3-{l-[6-(2aminopyrimidin-5yl)pyridin-3yl]cyclobutyl}-1,2,4oxadîazol-5-yl)-1Hpyrazol-1 -yljacetamide
71	AA^AtAx-A^ il \| ï W_xN 'T N ^U 1 A A H₂N N 0	5-{5-[l-(5-{l- [(methylsulfonyl)rn ethyl ]-1 H-pyrazol-4-yl} - 1,2,4-oxadiazol-3- yl)cyclobutyi]pyridin-2yl} pyrimidin-2-amine
72	0 AA-o n A n ^u A A h₂n n	5-(5- {4-[5-(pyridin-3- yl)-1,2,4-oxadiazol-3- yl]tetrahydro-2H-pyran- 4-yl}pyridin-2- yl)pyrimidin-2-amine

73	/= N ^ΝΌ^ A J Η₂Ν Ν	5-(5-{l-[5-(pyridin-3- yl)-l ,2,4-oxadiazol-3yl]cyclobutyl}pyrîdin-2- yl)pyrimidin-2-amine
74	Λ 2 η₂ν ν	5-(5-{l-[5-(6methylpyridin-3-yi)l,2,4-oxadiazol-3yljcyclobutyl} pyridin-2yI)pyrimidin-2-amine
75	Ο η AZV %_/¥ /Λ¹ ‘Ο A 3 η₂ν ν	5-(5-{ 1-(5-( 1Himidazol-4-yl)-1,2,4oxadiazol-3yljcyclobutyl} pyridin-2yl)pyrimidin-2-amine
76	îjitVnQ η₂ν^ι<	5-(5- {1 -[5-(pynOlidin- 1 -yl)-1,2,4-oxadiazol-3yljcyclobutyl} pyridin-2yl)pyrimidin-2-amine
77	COM3 Ν'Χ'Ν^ ^Ν'Ο V\ Λ J ⁰ η₂ν ν	3-(3-(1-(6-(2ammopyrimidin-5yl)pyridin-3yl]cyclobutyl}-l,2,4oxadiazol-5-yl)-lmethylpyridin-2( 1H)one
78	\Ζ Η JJUy¹ Ν Ν ^υ / A J η₂ν ν	5-(5-( I-[5-(3-methyl- 1 H-pyrazol-4-yl)-1,2,4oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine

79	ⁿ° ^M^n Λ J HjN N	5-(5-{l-[5-(lH-indazol- 5-yl)-1,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
80	<X> H /^N~N hï^/Y ° Λ b h₂n n	5-(5-{l-[5-(3-methyl- l H-pyrazol-5-yl)-1,2,4oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
81	AA/w A J N-o 0 N N ^U A J h₂n n	methyl 5-(3-{ l-[6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridine2-carboxylate
82	\Z κι r-N OH yuiaCA nAn ⁰ A X h₂n n	2-[5-(3-{l-[6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl}-1,2,4oxadiazol-5-yl)pyridin2-yl]propan-2-ol
83	rA'Mj ’ⁿ A fi N-_O ^z N > N ^υ A b h₂n n	5-(3-{l-[6-(2aminopyrimidin-5yl)pyridin-3yl]cyclobutyl} -1,2,4oxadiazol-5-yl)pyridine2-carbonitrile

84	/A V-C3* XX Ν-οΧ-Ν Η₂Ν'^>Χ'Ν'^>	5-(5-{1-[5-(2- chloropyridin-3-yl)l,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
85	π^ν-Ο ^{Ν 0} / ^Ν Λ J η₂ν ν	5-(5- {I-(5-(2methylpyridin-3-yl)l,2,4-oxadiazol-3yljcyc lobu t yl} pyridin-2yl)pyrimidin-2-amine
86	Γ J Ύ XvV ^ν'° ν	5-(5-(1-(5-(4methoxypyridin-3-yl)l,2,4-oxadiazol-3yljcyclobutyl} pyridin-2yl)pyrimidin-2-amine
87	οΧ-Ο Ν^Ν ^{Ν 0} A A η₂ν ν	5-(5-{l-[5-(pyridin-4- yl)-1,2,4-oxadiazol-3yl]cyclobutyl} pyridîn-2- yI)pyriinidin-2-amine
88	τ\Χ-·-ν r=\ xTl ^Cl η₂ν ν	5-(5-( 1-(5-(4chloropyridin-3-yl)l,2,4-oxadîazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
89	[*ΥΥ\_A \-Ν^/_^^ΧΟ ^Ν^° η₂ν^'ν'	5-(5-(1-(5-(6- (morpholin-4yl)pyridîn-3-yl]-1,2,4oxadiazol-3yl(cyclobutyl)pyridin-2yl]pyrimidin-2-amine

90	,-''Av^N. /’-’nh A- F n-o' ^n N Y N ^u A J h₂n n	5-(5-{ l-[5-(lH-pyrazol- 4-yl)- l ,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
91	N '^An ^{N 0 V}~ _OH H,N Y'	4-(3-( l-[6-(2aminopyrimidin-5 yl)pyridin-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)pyridin2-ol
92	rAv-O ⁿ'° ⁿ Λ d h₂n n	5-(5- {l -[5-(pyrimidin-4- yl)-1,2,4-oxadiazol-3- yl]cyclobutyl}pyridin-2- yl)pyrimidin-2-amine
93	rorvo N^/A ^{N 0} Ad ° h₂n n	5-(5-(1-(5-(2- methoxypyridin-4-yl)l,2,4-oxadîazol-3yl]cyclobutyl}pyridin-2yl)pyrimîdin-2-amine
94	rrryA nYZV ⁿ'° ^s^ h₂n'^n'	5-(5-(1-(5-(2,4- dimethyl-1,3-thiazol-5yl)-1,2,4-oxadîazol-3yl]cyclobutyl}pyridin-2yl)pyrimîdin-2-amine
95	<A °w ^H A J h₂n n	3-(3-(1-(6-(2aminopyrimidîn- 5 yl)pyridin-3yl (cyclobutyl) -1,2,4oxadiazol-5-yl)pyridin-

		2(lH)-one
96	pXry£yo_x ^N-O >^Nh/J	5-(5-( 1-(5-(2,6- dimethoxypyridin-3-yl)l,2,4-oxadiazol-3yl]cyciobutyl}pyridin-2yl)pyrimidin-2-amine
97	CCîVO N^r_fr^{J N}-° >^Na J ^H0 h₂n n	3-(3-(1-(6-(2aminopyrimidin-5yl)pyridin-3yl]cyc lobutyl}-1,2,4oxadiazol-5-yl)-6methylpyridin-2-ol
98	X/ ”'O °^J A 4 h₂n n	5-(5- {1 -[5-( 1,3-oxazol- 5-yl)-1,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
99	^X-yj-yc, y/ ⁿ~° A 4 h₂n n	5-(5-(1-(5-(6chloropyridin-3-yl)l,2,4-oxadiazol-3yl ]cyc lobutyl} pyridin-2 yl)pyrimidin-2-amine
ΙΟΟ	n^v-O X fi N-η n yr N ^υ A fi H₂N N	5-(5-( l-[5-(pyrimidin-5yl)-1,2,4-oxadiazol-3yl]cyclobutyl}pyridîn-2yl)pyrimidin-2-amine
101	rpy-O ⁿ-° a A 4 h₂n n	5-(5-(1-(5-(2- methylpyridin-4-yl)l,2,4-oxadîazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine

102	J Ν-Π Λ J η₂ν ν	5-(5- {1-(5-( 1-methyl- 1 H-pyrazol-4-yl)-1,2,4oxadiazol-3yljcyc lobutyl} pyridin-2 yl)pyrimîdîn-2-amine
103	(ΥϊΑνΑ L Jl L'y ν Υν ° / ηΑ	5-(5-(1-(5-(3,5dimethyl-1 H-pyrazol-4yl)-1,2,4-oxadiazol-3yljcyclobutyl} pyridin-2 yl)pyrimidin-2-amine
104	Α^νγΟ nXV ^Ν'θ ^χ=νΛ J η₂ν ν	5-(5- (1 -[5-(pyridazin-4yl)-1,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
105	<Α ^Η2^Ν Ν ^:>' Ν ⁰ Λ ) η₂ν ν	5-(5-(1-(5-(2- aminopyridin-3-yl)l,2,4-oxadîazol-3yl] cyc lobutyl} pyridin-2 yl)pyrimidin-2-amine
106	r/^v-O _ΝΑγ ^Ν'° f Λ ) ^Η*^Ν η₂ν ν	5-(5-(1-(5-(4aminopyridm-3-yl)l,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
107	\/ Γ-Ν νΧΥ ^Ν-θ ν A J ^Η0 η₂ν ν	3-(3-(1-(6-(2aminopyrimidin-5yl)pyridin-3yl]cyclobutyl}-l,2,4oxadiazol-5-yl)pyridin4-o 1

108	^N'O ^Vn A k ^H h₂n n	5-(3-(1-(6-(2aminopyrimidin- 5yl)pyridîn-3yljcyclobutyl} -1,2,4oxadiazol- 5 -yl )pyridin2(1 H)-one
109	X J N-O A N Ί ^N F-A ^{F F}	5-[5-(l-{5-[2- ( tri fluoromethyl)pyridin -3-yl]-1,2,4-oxadiazol- 3-yl]cyclobutyl)pyridin- 2-yl]pyrimidin-2-amine
HO	AnAA nA^{n 0} A k h₂n n	5-(5-(1-(5-(6- (dimethylamino)pyridin3-yl]-l,2,4-oxadiazol-3yl} cyclobutyl)pyridin-2yl]pyrimidin-2-amine
lll	A-Mn /=\_ ⁰ A J h₂n n	5-(5-( 1-(5-(6- aminopyridin-3-yl)l,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
112	Αχχ Ν'^γ^Ν ⁰ h₂n'^'n'^x	5-(5-( 1-(5-(6- (pyrrolidin-l-yl)pyridin- 3-yl]-l,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
113	υ··-Α<,·ν A Ad _X.AA4/'' Ν 'γ \ ° A J h₂n n	5-(5-(1-(5-(6(methylamino)pyridin3-yl]-1,2,4-oxadiazol-3yl} cyclobutyl)pyridin-2yl]pyrimidin-2-amine

114	n^y-O-y _NaV ⁿ'° / Λ J h₂n n	5 - [5-( 1 -{5-[6-(propan-2ylamino)pyridin-3-yl]l,2,4-oxadîazol-3yl}cyclobutyl)pyridîn-2yl]pyrimidin-2-amine
ll5	ααΜα ζ=Λ H ΑΠχΑ Tj ^N hoV h₂n^n^	2-((5-(3-( 1-(6-(2- aminopyrimidîn-5yl)pyridin-3yljcyclobutyl}-1,2,4oxadiazol-5-yl)pyridin- 2-yl] amino} éthanol
H6	.^AACn /=N / jfjy xOⁿ^^ohnAt ™ ⁰ A J h₂n n	2-((5-(3-(1-(6-(2aminopyrimidin-5yl)pyridin-3yljcyclobutyl}-1,2,4oxadiazol-5-yl)pyridin2yl](methyl)amino}ethan ol
H7	^AA-n /=N / N'At’N ⁰ A J h₂n n	5-(5-(1-(5-(6-((2methoxyethyl)(methyl)a mino]pyridin-3-yl}- l,2,4-oxadiazol-3yl)cyclobutyl]pyridin-2yl} pyrimidin-2-amine
118	S.AC„ N /=N H 1Y1 yAA ⁿ'° A J h₂n n	5-(5-(1-(5-(6-((2methoxyethyl)amino]py ridin-3-yl}-1,2,4oxadiazol-3yl)cyclobutyl]pyridîn-2yl} pyrimidin-2-amine

ll9	XAv'^N A^N \ /LO ΥΠΑΗ N '^f N ⁰ A J h₂n n	5-[5-(l-{5-[6(methylsulfonyl )pyridin3-yl]-l,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2yl]pyrimidin-2-amine
120	/A Γ II Y J—NH Νγ_Ν ^{; n}-° ⁿh₂n^Zn^	5-(5-( 1-(5-(1 H-1,2,4tri azol-3-yl)-1,2,4oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amîne
I2l	pYyYY N-oA'N A J ^z H₂N N	5-(5-(1-(5-(1,3dimethyl-1 H-pyrazol-5yl)-l,2,4-oxadiazol-3yljcyclobutyl} pyridin-2yl)pyrimidin-2-amine
122	xFA n^a n ⁰ A J h₂n n	5-(5-(1-(5-(2(methylamino)pyridin3-yl]-l,2,4-oxadiazol-3yl} cyclo butyl )pyridin-2yl]pyrimidin-2-amine
123	nXvo /M A F N-_o s N 7 N ^υ A J h₂n n	5-(5-( 1 -[5-( 1,3-thiazol- 5-yl )-1,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
124	Aisⁿ'>Aⁿ ,/7/ ^N~° ,^N A J h₂n n	5-(5-( 1-(5-( 1-methyl- 1 H-pyrazol-5-yl)-l ,2,4oxadîazol-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine

125	z\ 0 X _N «N /Ά Aï AAZAⁿ_-^nh A J h₂n n	4-(5-(3-( 1-(6-(2- aminopyrimidin-5yl)pyridin-3yl]cyclobutyl}-1,2,4oxadiazol-5-yl)pyridin2-yl]piperazin-2-one
126	yX _Ν.χχ_Ν	5-(5-(1-(5-(2(dimethylamino)pyridin3-yl]-1,2,4-oxadiazol-3yl} cyclobutyl)pyridin-2yl]pyrimidin-2-amine
127	n^v-A Av ⁿ-° ⁿ H₂N'^n'^X	5-(5-( 1-(5-( 1-methyl- 1 H-pyrazol-3-yl)-1,2,4oxadîazol-3yljcyclobutyl} pyridin-2yl)pyrimidin-2-amine
128	/'TV ⁿ~0 >N A O CW	5-(5-(1-(5-(2- (morpholin-4yl)pyridin-3-yl]-1,2,4oxadiazol-3yl} cyclobutyl )pyridin-2yl]pyrimidin-2-amine
129	n^vp X- A JJ N-n^Z x—N N Ά N ^u A J h₂n n	5-(5- {l-[5-(pyrazin-2- yl)-l,2,4-oxadiazoi-3yl]cyclobutyl}pyridin-2- yl)pyrimidin-2-amine
130	n^v-A A JJ N-n ^-^N N ^' N ⁰ A J h₂n n	5-(5-(1-(5-(5- methylpyrazin-2-yl)l,2,4-oxadiazol-3yljcyclobutyl} pyridin-2yl)pyrîmidin-2-amine

131	nA/ 'O N' A J H₂N N	5-(5-{l-[5-(l-methyl- l H-imidazol-4-yl)- l,2,4-oxadiazoi-3yl]cyclobutyl}pyridin-2yl)pyrimidin-2-amine
132	A J h₂n n	5-(6-{l-[5-(lH-pyrazol- 4-yl)-1,2,4-oxadiazol-3yl]cyclobutyl}pyridin-3- yl)pyrimidin-2-amine
133	\ / ^H Yx X^N N-N \|ÏA AA A N-ο x-A η₂ν^γτ	5-(6-{l-[5-(3-methyl- l H-pyrazol-5-yl)-1,2,4oxadiazol-3yl]cyclobutyl} pyridin-3 yl)pyrimidin-2-amine
134	^AAL-n λ=^ν ATA yAvA _n^yxA/N n-o A 7 H₂N N	5-(6-{l-[5-(l-methyllH-pyrazol-4-yl)-1,2,4oxadiazol-3yl]cyclobutyl}pyridin-3- yl)pyrimidin-2-amine
135	YW _nz/A^{n n}o T A J h₂n n	5-(6-{l-[5-(3-methyllH-pyrazol-4-yl)-l,2,4oxadiazol-3yl]cyclobutyl}pyridin-3yl)pyrimidin-2-amine
136	0 xXn i r T A w > _n^AU a a A J ^x h₂n n	5-(6-{4-[5-(l,3dimethyl-1 H-pyrazol-5yl)-1,2,4-oxadiazol-3yl]tetrahydro-2H-pyran- 4-yl}pyridin-3- yI)pyrimidin-2-amine

137	zJXz Z\ AUV---n αΊ) h₂n n	5-(6- {4-[5-(pyridîn-3 yl)-l,2,4-oxadiazol-3yl ] tetrahydro-2 H-pyran4-yl}pyridin-3- yl)pyrimidin-2-amine
138	0 /N-JXL-N AAi ÎJ h₂n n	5-(6-{4-[5-(pyridin-4- yl)-l,2,4-oxadiazol-3yl]tetrahydro-2H-pyran4-yl}pyridin-3yl)pyrimidin-2-amine
139	xaJAAn /=n ATi-₀Z»_rP n >'n Lv-'o H₂N' 'N	5-[5-(l-{5-[l-(l,ldioxidotetrahydrothioph en-3-yl)-1 H-pyrazol-4yl]-1,2,4-oxadiazol-3yl} cyclobutyl )pyridin-2yl]pyrimidin-2-amine
140	/*n ^XjijAn na< n ^υ / η₂ν^ΛΧ A^o	5-{5-[l-(5-{ l-[2(morpholin-4-yl)ethyl]l H-pyrazol-4-yl} -1,2,4oxadiazol-3yl)cyclobutyl]pyridin-2yl}pyrimidin-2-amine
I4l	Χαζ /=n zjjïo^^N^ N N ^u A J n h₂n n n	[4-(3-{l-[6-(2aminopyrimidin-5yl)pyridin-3yl]cyc lobutyl}-1,2,4oxadiazol-5-yl)-1Hpyrazol-l-yl]acetonitrile

142	υΧλ a h T « Avn_x /•YY N-o Ί νΥν ^υ I _ A J X h₂n n I	5-{5-[]-(5-{l-[2(dimethylamino)ethyl]l H-pyrazol-4-yl} -1,2,4oxadiazol-3yl)cyclobutyl]pyridin-2yl} p yrimidin-2-amine
143	ΑΠ-οΑ A J cAa h₂n n	2-[4-(3-{l-[6-(2aminopyrimidin-5yl)pyridîn-3yljcyclobutyl} -1,2,4oxadiazol-5-yl)-1Hpyrazol-1 -yl]-N-tertbutyl-Nmethylacetamide
144	ATXA N N ^U A J <ΥΝΗ h₂n n	2-(4-(3-(l-[âYaminopyrimidin-Syl)pyridin-3yljcyclobutyl}-! ,2,4oxadiazoI-5-yI)- ï Hpyrazoi-1 -yl]-N-tertbutylacetamide
145	/-'>,.Χ_ν,Ν /==N h₂n n	5-(5-( l-[5-(l-oxetan-3yl-1 H-pyrazol-4-yl)- [ l ,2,4]oxadiazol-3-yIJcyclobutyl} -pyridin-2yl)-pyrazin-2-yl amine

146	H, AfT / °^H	l-[4-(3-{i-[6-(5-aminopyrazin-2-yl)-pyridin-3yl]-cyclobutyl}[l,2,4]oxadiazol-5-yl)pyrazol -1 -yl ]-2-methylpropan-2-ol
147	\ A. . N A^N AAA· A J Λ° H,N N Γ ² nh₂	3-[4-(3- {l-[6-(2-amino- pyrimidin-5-yl)-pyridin- 3-yl]-cyclobutyl}- [l,2,4]oxadiazol-5-yl)pyrazol-l-yl]-2,2dimethyl-propionamide
148	zaAA-n aⁿ ARaS/ 1T^N bb h₂n n	3-[4-(3- {1 -[6-(2-amino- pyrimidin-5-yl)-pyridîn- 3-yl]-cyclobutyl}- [l,2,4]oxadiazol-5-yl)pyrazol-l-yl]-2,2dimethyl-propionitrile

149	yxJA-n λν „,ί Τ ϊ₀Κυ, Ν Ν ^υ Γ η₂ν^ΛΧ ^{0 ΝΗ}>	2-[4-(3 - {I -[6-(2-aminopyrimidin-5-yl)-pyridin3-yl]-cyclobutyl}[ l ,2,4]oxadiazol-5-yl)pyrazol-l-yl]isobutyramîde
150	X ν-Α νΥν ° Α η₂ν^ΛΧ ^ηΑ	5-(5-( l-{5-[l-(2-amino- 2-methyl-propyl)-1Hpyrazol-4-yl][l,2,4]oxadiazol-3-yl}cyclobutyl)-pyridin-2yl ]-pyrimidin-2-yl amine
I5l	Αϊ ΎχΥγ Ν Ν ^υ η₂ν'^'ν' ν	2-[4-(3-{ l-[6-(2-aminopyrimidin-5-yl)-pyridin3-yl]-cyciobutyl}[ l ,2,4]oxadiazol-5-yl)pyrazol-1 -yi]-2-methylpropionitrile
152	^ΑΑ^ν /=ν ΑΠΑγ A ΑΧ Ν ^υ Vo η/ίΆ	5- {l -[5-( l -oxetan-3-yllH-pyrazol-4-yl)[ l ,2₎4]oxadiazoI-3-yl]cyclobutyl}jZ^^bipyridinyl-ô'ylamine
153	^\XLn /=ν _χ _/^Χ1ν'Ο^'^Ν ^^οη γ[^{Ν υ} η₂νΑ	l-(4-{3-[l-(6'-amino[2,3']bipyridinyl-5-yl)cyclobutyl]- [ l ,2,4]oxadiazol-5-yl} -

155	A'.jK/N /*n h κιΎ HN^O H₂N n	2-[4-(3-{l-[6-(2-Aminopyrimidin-5-yl)-pyridin3-yl]-cyclobutyI}- [ 1,2,4]oxadiazol-5-yl)pyrazol-l-yl]-Ncyciopropyl-acetamide
156	ζαΑ··Ν /=n aïu-a N N ^u n HN'Sd H,N N I X	2-(4-(3-( l-tô-tf-aminopyrimidin-S-yO-pyridin3-yl]-cyclobutyl}- [ 1,2,4]oxadiazol-5-yl)pyrazol-l-yl]-N(tetrahydro-furan-2ylmethyl)-acetamide
157	/n Ν-γΟ^^{0 x Ν}γ ÂJ HN^O H₂N N ^Ax.	2- (4-(3- {1 -[6-(2-amino- pyrimidin-5-yl)-pyridin- 3- yl]-cyclobuty 1)-(1,2, 4]oxadiazoi-5-yl)pyrazol-l-yi]-N-i sopropyl-acetamide
158	ΑΥΧτΑ ..A J HlAo h₂n n	2- (4-(3- {1 -[6-(2-aminopyrimidin-5-yl)-pyridin- 3- yl]-cyciobutyI}-[ 1,2, 4]oxadiazol-5-yl)- pyrazol-l-yl]-N-ethylacetamide

159	N ^{x Ν}χ Λ ) -ν^Λο l-LN N I Z	2- [4-(3-{ l-[6-(2-amino- pyrimidin-5-yl)-pyridin- 3- yl]-cyclobutyl}-[l,2, 4]oxadiazol-5-yl)pyrazol-1 -yl]-N-methyl- N-(tetrahydro-furan-2ylmethyl)-acetamîde
160	/=n N +/ N ^υ 1 Λ J ν^Λο H₂N N	2- [4-(3-{ l-[6-(2-aminopyrimidin-5-yl)-pyridin- 3- yl]-cyclobutyl}-[ 1,2, 4]oxadiazol-5-yl)- pyrazol-l-yl]-Ncyclopropyl-N -methyl acetamide

161	υΑΑν λ=ν UUÏoA A J Λν^ζ:ϊό h₂n n - o	2- [4-(3-{ l-[6-(2-aminopyrimidin-5-yl)-pyridin- 3- yl]-cyclobutyl}-[!,2, 4]oxadiazol-5-yl)pyrazol-l-yl]-l-(3- methoxy-pyrrolidin-1 yl)-ethanone
162	^{X Ν}Ί A J Ao h₂n n	2- [4-(3-{l-[6-(2-aminopyrimidin-5-yl)-pyridin- 3- yl]-cyclobutyl}-[l,2, 4]oxadiazol-5-yl)- pyrazol-1 -yl]-N-ethyl- N-methyl-acetamide
163	^υ>Αν /=n o ΑΠ-ο^ ηΑ’Ν	2-(4-{3-[l-(6'-amino- [2,3’]bipyridinyl-5-yl)cyclobutyl]- [ 1,2,4] oxadîazol-5-yl} - pyrazol-l-yl)-N,Ndimethyl-acetamide
164	ζ-υΑ,Λ A^N rA A, Η,Ν^Ν^ ⁰ N	2-[4-(3-{l-[6-(5-aminopyrazin-2-yl)-pyridin-3yl]-cyclobutyl}[ 1,2,4]oxadiazol-5-yl)pyrazol-1 -yl]-N,Ndimethyl-acetamide

165	/=sn ηΑγΑ Γ oh I	2-Methyl-l-[4-(3-{l-[6(2-methylaminopyrimidin-5-yl)-pyridin3-yl]-cyclobutyl}[ l ,2,4]oxadîazol-5-yl)pyrazol-1 -yl]-propan-2ol
166	χ+AvN. /^Ν _χ ^Ν <α-ⁿà_h	6’-Amino-5-( l-{5-[ l -(2hydroxy-2-methylpropyl)-1 H-pyrazol-4yl]-[ l,2,4]oxadiazol-3yl}-cyclobutyl)[2,3']bipyridinyl-5’carbonitrile
167	-î^AA-n /*ν ^Ν U, H-.N'^hT	6’-Amino-5-{l-[5-(l- oxetan-3-yl-1 H-pyrazol4-yl)-[ l ,2,4]oxadiazol3-yl]-cyclobutyl}fZ^'Jbipyridinyl-S'carbonitrile
168	Α·Αν_χ /=ν [ Il « A^vn^ <^ΝγΑ ^Ν'° Η	Methyl-[5-(5-{l-[5-( l methyl-1 H-pyrazol-4yl)-[ l ,2,4]oxadiazol-3yl]-cyclobutyl}-pyridin2-yl)-pyrazin-2-yI]amine
169	ζ<''-νΑ..=.Ν /=Ν ί Y “ αΥν ΑχΑ ^N-°^r₀ Η₂Ν^>''ν'·'''	6-Methyl-5-(5-{ l-fS-floxetan-S -yl- 1 H-pyrazo 1 4-yl)-[l,2,4]oxadiazol3-yl]-cyclobutyl}pyridin-2-yl)-pyrazin-2-

		ylamine
170	.A-Αγ /*n Γ II « >Ύν A ,γΜ NV η₂ν^ν^	[4-(3- {1 -[6-(5-Aminopyrazin-2-yl)-pyridin-3yl]-cyclobutyl}- [ l,2,4]oxadiazol-5-yl)pyrazol-l-yl]acetonitrile
171	HjN^N	5-(5-( 1 -(5-(1-(2Methoxy-ethyl)-1Hpyrazol-4-yl]- [ l^^oxadiazol-S-ylîcyclobutylJ-pyridin-Zyll-pyrazm-Z -ylamine
172	/==:Ν ϊξΑΑ Η_?Ν Ν ^ν / ΟΗ	1-(4-(3-( l-[6-(5-Amino- 3-methyl-pyrazin-2-yl)pyridin-3-yl]cyclobutyl}- (l,2,4]oxadiazol-5-yl)pyrazol-1 -yl]-2-methylpropan-2-ol
173	^xJxLm /=Ν n £ ϊ S Υ > <^ΝγΎ ^Ν'° ην^Α 1	[4-(3-(1-(6-(5- Methylamino-pyrazin-2yl)-pyridin-3-yl]cyclobutyl}- [ 1,2,4]oxadiazol-5-yl)pyrazol-l-yl]acetonitrile

174	h₂n X	5-(5-{ 1-(5-( 1-Methyl- lH-pyrazol-4-yl)- [l,2,4]oxadiazol-3-yl]cyclobutyl}-pyridin-2yl)-pyrazîn-2-ylamine
175	yAxAti /=*n _{x z} 1 £ J S Ali,A AV ⁿ-° ^oh A J h₂n n	1-(4-(3-( 1-(6-(2-Amîno- 4-methyl-pyrimidin-5yl)-pyridin-3-yl]cyclobutyl}- [ 1,2,4]oxadiazol-5-yl)pyrazol-1 -yl]-2-methylpropan-2-ol
176	jJa» ^xnAo HN^N 1	Methyl-[5-(5-( 1-(5-(1oxetan-3-yl-1 H-pyrazol- 4-yl)-[ 1,2,4]oxadiazol3-yl]-cyclobutyl(pyridin-2-yl)-pyrazin-2yl]-amine
177	/Vy\ Λν HN^IT / θ^Η 1	2-Methyl-l -(4-(3-(1 -(6(5-methylaminopyrazin-2-yl)-pyridin-3yl ]-cyc lo butyl }[ 1,2,4]oxadiazol-5-yl)pyrazol-l-yl]-propan-2ol

or the pharmaceutically acceptable salts thereof

In one embodiment, the invention relates to any of the compounds depicted in Table l above and the pharmaceutically acceptable sait thereof.

Représentative compounds ofthe invention show activity in the FLAP binding assay and in the human whole blood LTB₄ production inhibition assay, described in the assessment of biological properties section, as shown in Table IL

Table II

Example	FLAP SPA IC₅o (nM)	hWB LTB₄ IC_so (nM)
l	3.8	280
2	5.0	740
3	2.7	150
4	17	430
5	8.8	1100
6	5.8	830
7	11	690
8	2.0	110
9	2.9	320
10	30	650
11	78	2200
12	2.1	140
13	3.9	170
14	140	>5000
15	280	2600
16	11	2200
17	8.7	>5000
18	1.8	95
19	58	>5000
20	9.2	530
21	2.6	250
22	2.5	140
23	26	430
24	110	1000

25	4.0	46
26	110	730
27	12.4	420
28	17	210
29	35	320
30	33	400
31	1.9	300
32	2.9	140
33	2.2	2600
34	40	1800
35	43	>5000
36	5.9	1400
37	110	790
38	3.2	75
39	3.7	86
40	3.3	92
41	7.7	>5000
42	7.7	>5000
43	1.2	170
44	2.7	100
45	3.1	750
46	2.4	110
47	3.4	170
48	2.2	140
49	3.7	180
50	2.7	150
51	4.8	150
52	2.6	180
53	2.6	2600
54	28	120

55	13	52
56	3.2	24
57	2.4	34
58	22	250
59	83	610
60	7.9	150
61	1.8	41
62	2.6	72
63	8.8	190
64	7.2	170
65	590	>5000
66	7.4	200
67	9.5	69
68	6.1	160
69	7.6	170
70	150	2100
71	58	390
72	610	2300
73	25	460
74	4.5	210
75	19	580
76	92	920
77	51	490
78	4.7	220
79	4.0	68
80	5.5	160
8I	25	790
82	17	480
83	52	410
84	4.1	280

85	21	1000
86	18	llOO
87	55	1000
88	7.3	490
89	2.7	180
90	7.0	140
91	24	330
92	130	2200
93	9.6	400
94	8.1	650
95	29	>5000
96	7.3	HOO
97	19	>5000
98	HO	>5000
99	7.5	660
ΙΟΟ	120	960
ΙΟΙ	24	820
102	13	270
103	14	1000
104	HO	2100
105	17	570
106	31	840
107	190	4000
108	48	720
109	14	1500
HO	2.4	310
lll	4.2	74
ll2	3.3	570
U3	2.4	100
H4	1.5	280

115	1.9	49
116	4.3	140
117	3.0	120
118	2.8	84
119	62	230
120	200	>5000
121	28	1800
122	28	3800
123	31	790
124	11	210
125	1.8	160
126	34	>5000
127	40	640
128	66	2700
129	47	630
130	26	350
131	52	300
132	46	370
133	43	340
134	81	790
135	27	400
136	540	>5000
137	580	3000
138	970	>5000
139	28	340
140	15	110
141	11	85
142	16	250
143	14	260
144	14	190

145	8.3	29
146	15	43
147	65	340
148	25	200
I49	160	430
150	68	370
I5l	18	94
152	13	100
153	34	190
154	170	590
155	63	550
156	97	620
157	79	560
158	100	550
159	83	510
160	95	540
I6l	250	1100
162	130	490
163	110	300
164	43	170
165	73	280
166	200	740
167	140	680
168	33	99
169	-	21
170	48	51
171	50	76
172	-	51
173	-	18
174	39	74

175	830	620
176	23	73
177	32	160

The invention also relates to pharmaceutical préparations, containing as active substance one or more compounds of the invention, or the pharmaceutically acceptable dérivatives thereof, optionally combined with conventional excipients and/or carriers.

Compounds ofthe invention also include their isotopically-labelled forms. An isotopically-labelled form of an active agent of a combination of the présent invention is identical to said active agent but for the fact that one or more atoms of said active agent hâve been replaced by an atom or atoms having an atomic mass or mass number different from the atomic mass or mass number of said atom which is usually found in nature. Examples of isotopes which are readily available commercially and which can be incorporated into an active agent of a combination of the présent invention in accordance with well established procedures, include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine and chlorine, e.g., ²H, ³H, ^l3C, ^l4C, ^l5N, ¹⁸O, ^l70,³¹ P, ³²P, ³⁵S, ^lltF, and ³⁶C1, respectively. An active agent of a combination of the présent invention, a prodrug thereof, or a pharmaceutically acceptable sait of either which contaîns one or more of the above-mentioned isotopes and/or other isotopes of other atoms is contemplated to be within the scope of the présent invention.

The invention includes the use of any compounds of described above containing one or more asymmetric carbon atoms may occur as racemates and racemic mixtures, single enantiomers, diastereomeric mixtures and individual diastereomers. Isomers shall be defined as being enantiomers and diastereomers. Ail such isomeric forms of these compounds are expressly included in the présent invention. Each stéréo génie carbon may be in the R or S configuration, or a combination of configurations.

Some of the compounds of the invention can exist in more than one tautomeric form. The invention includes methods using ail such tautomers.

Ail terms as used herein in this spécification, unless otherwise stated, shall be understood in their ordinary meaning as known in the art. For example, “Cm alkoxy” is a Cmalkyl with a terminal oxygen, such as methoxy, ethoxy, propoxy, butoxy. Ail alkyl, alkenyl, and alkynyl groups shall be understood as being branched or unbranched where structurally possible and unless otherwise specified. Other more spécifie définitions are as follows:

The term “alkyl” refers to both branched and unbranched alkyl groups. It should be understood that any combination term using an “alk” or “alkyl” prefix refers to analogs according to the above définition of “alkyl”. For example, terms such as “alkoxy”, “aikythîo” refer to alkyl groups linked to a second group via an oxygen or sulfur atom. “Alkanoyl” refers to an alkyl group linked to a carbonyl group (C=O).

In ail alkyl groups or carbon chains, one or more carbon atoms can be optionally replaced by heteroatoms such as O, S or N. It shall be understood that if N is not substituted then it is NH. It shall also be understood that the heteroatoms may replace either terminal carbon atoms or internai carbon atoms within a branched or unbranched carbon chain. Such groups can be substituted as herein above described by groups such as oxo to resuit in définitions such as but not limited to: alkoxycarbonyl, acyl, amido and thioxo.

As used herein, “nitrogen” and “sulfur” include any oxidized form of nitrogen and sulfur and the quatemized form of any basic nitrogen. For example, for a -S-Cm alkyl radical, unless otherwise specified, shall be understood to include -S(O)-Cm alkyl and -S(O)2-Cm alkyl.

The term Cm hydroxy also means Cijalkylhydroxy or Ci.^alkyl-OH.

The term “C3.10carbocycle” or “Cj.iocycloalkyl” refers to a nonaromatic 3 to IOmembered (but preferably, 3 to 6-membered) monocyclic carbocyclic radical or a nonaromatic 6 to 10-membered fused bicyclic, bridged bicyclic, or spirocyclic carbocyclic radical. The C3-10 carbocycle may be either saturated or partially unsaturated, and the carbocycle may be attached by any atom of the cycle which results in the création of a stable structure. Non-limiting examples of 3 to 10-membered monocyclic carbocycles include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptanyl, cycloheptenyl, and cyclohexanone. Nonlimiting examples ofô to 10-membered fused bicyclic carbocyclic radicals include bicyclo[3.3.0]octane, bicyclo[4.3.0]nonane, and bicyclo[4.4.0]decanyl (decahydronaphthalenyl). Non-limiting examples of 6 to 10-membered bridged bicyclic carbocyclic radicals include bicyclo [2.2.2]heptanyl, bicyclo[2.2.2]octanyl, and bicyclo[3.2.l]octanyl. Non-limiting examples of 6 to 10-membered spirocyclic carbocyclic radicals include but are not limited to spiro[3,3]heptanyl, spiro[3,4]octanyl and spiro[4,4]heptanyl.

The terrn “C^o aryl” or “aryl” refers to aromatic hydrocarbon rings containing from six to ten carbon ring atoms. The terrn C^-io aryl includes monocyclic rings and bicyclic rings where at least one of the rings is aromatic. Non-limiting examples of Cô.io aryls include phenyl, indanyl, indenyl, benzocyclobutanyl, dihydronaphthyl, tetrahydronaphthyl, naphthyl, benzocycloheptanyl and benzocycloheptenyl.

The terrn ”5 to 11-membered heterocycle” refers to a stable nonaromatic 4-8 membered monocyclic heterocyclic radical or a stable nonaromatic 6 to l l-membered fused bicyclic, bridged bicyclic or spirocyclic heterocyclic radical. The 5 to 1 l-membered heterocycle consists of carbon atoms and one or more, preferably from one to four heteroatoms chosen from nitrogen, oxygen and sulfur. The heterocycle may be either saturated or partially unsaturated. Non-limiting examples of nonaromatic 4-8 membered monocyclic heterocyclic radicals include tetrahydrofuranyl, tetrahydropyranyl, oxetanyl, azetidinyl, pyrrolidinyl, dihydropyridinyl, pyranyl, tetrahydropyranyl, dioxanyl, thiomorpholinyl, l,l-dioxo-lk⁶-thiomorpholinyl, morpholinyl, piperidînyl, piperazinyl, and azepinyl. Non-limiting examples of nonaromatic 6 to 1 l-membered fused bicyclic radicals include octahydroindolyl, octahydrobenzofuranyl, and Ά octahydrobenzothiophenyl. Non-limiting examples of nonaromatic 6 to 11-membered bridged bicyclic radîcals include 2-azabicyclo[2.2. IJheptanyl, 3azabicyclo[3.l.0]hexanyl, and 3-azabicyclo[3.2.l]octanyl. Non-limiting examples of nonaromatic 6 to 11-membered spirocyclic heterocyclic radicals include 7-azaspiro[3,3]heptanyl, 7-spiro[3,4]octanyl, and 7-aza-spiro[3,4]octanyl.

The term “5 to 11-membered heteroaryl” shall be understood to mean an aromatic 5 to 6membered monocyclic heteroaryl or an aromatic 7 to 11-membered heteroaryl bicyclic ring where at least one of the rings is aromatic, wherein the heteroaryl ring contains l-4 heteroatoms such as N, O and S. Non-limiting examples of 5 to 6-membered monocyclic heteroaryl rings include furanyl, oxazolyl, isoxazolyl, oxadîazolyl, thîazolyl, pyrazolyl, pyrrolyl, îmidazolyl, tetrazolyl, triazolyl, thienyl, thiadiazolyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, and purînyl. Non-limiting examples of 7 to 11membered heteroaryl bicyclic heteroaryl rings include benzimidazolyl, quinolinyl, dihydro-2/7-quinolinyl, isoquinolinyl, quinazolinyl, indazolyl, thieno[2,3-d]pyrimidinyl, indolyl, isoindolyl, pyrazolopyrîmidinyl, imidazopyrimidinyl, benzofuranyl, benzopyranyl, benzodioxolyl, benzoxazolyl and benzothiazolyl.

It will be understood that one to three carbon ring moieties in the each of the C3.10 carbocyclic rings, the 5 to 1 l-meinbered heterocyclic rings, the nonaromatic portion of the bicyclic aryl rings, and the nonaromatic portion of the bicyclic heteroaryl rings can independently be replaced with a carbonyl, thiocarbonyl, or iminyl moiety, i.e., -C(=O)-, -C(=S)- and -C(=NR⁸)-, respectively, where R^K is as defined above.

The term “heteroatom” as used herein shall be understood to mean atoms other than carbon such as O, N, and S.

The term “halogen” as used in the présent spécification shall be understood to mean bromine, chlorine, fluorine or iodîne. The définitions “halogenated”, “partially or fully halogenated”; partially or fully fluorinated; “substituted by one or more halogen atoms”, includes for example, mono, di or tri halo dérivatives on one or more carbon atoms. For alkyl, a non-limiting example would be -CH2CHF2, -CF3 etc. A'”

Each alkyl, carbocycle, heterocycle or heteroaryl, or the analogs thereof, described herein shall be understood to be optionally partially or fully halogenated.

The compounds of the invention are only those which are contemplated to be ‘chemically stable’ as will be appreciated by those skilled in the art. For example, a compound which would hâve a ‘dangling valency’, or a ‘carbanion’ are not compounds contemplated by the inventive methods disclosed herein.

The invention includes pharmaceutically acceptable dérivatives of compounds of formula (I). A pharmaceutically acceptable dérivative refers to any pharmaceutically acceptable sait or ester, or any other compound which, upon administration to a patient, is capable of providing (directly or indirectly) a compound useful for the invention, or a pharmacologically active métabolite or pharmacologically active residue thereof. A pharmacologically active métabolite shall be understood to mean any compound ofthe invention capable of being metabolîzed enzymatically or chemically. This includes, for example, hydroxylated or oxidized dérivative compounds of the invention.

Pharmaceutically acceptable salts include those derived from pharmaceutically acceptable inorganic and organic acids and bases. Examples of suitable acids include hydrochloric, hydrobromic, sulfuric, nitric, perchlorîc, fumaric, maleic, phosphorîc, glycolic, lactic, salicylic, succînic, toluene-p-sulfuric, tartaric, acetic, citric, methanesulfonic, formic, benzoic, malonic, naphthalene-2-sulfuric and benzenesulfonic acids. Other acids, such as oxalic acid, while not themselves pharmaceutically acceptable, may be employed in the préparation of salts useful as intermedîates in obtaining the compounds and their pharmaceutically acceptable acid addition salts. Salts derived from appropriate bases include alkali métal (e.g., sodium), alkaline earth métal (e.g., magnésium), ammonium and N-(C 1-C4 alkyl)4⁺ salts.

In addition, within the scope of the invention is use of prodrugs of compounds of the invention. Prodrugs include those compounds that, upon simple chemical transformation, are modified to produce compounds of the invention. Simple chemical transformations include hydrolysis, oxidation and réduction. Specifically, when a prodrug is administered to a patient, the prodrug may be transformed into a compound disclosed hereinabove, thereby imparting the desired pharmacological effect.

The compounds of formula I may be made using the general synthetic methods described below, which also constitute part of the invention.

GENERAL SYNTHETIC METHODS

The invention also provides processes for making compounds of Formula (I). In ail Schemes, unless specified otherwise, R¹, R², R³, R⁴ and R⁵ in the Formulas below shall hâve the meaning ofR^R^R⁵, R⁴ and R⁵ în Formula (I) of the invention described herein above.

Optimum reaction conditions and reaction times may vary depending on the particular reactants used. Unless otherwise specified, solvents, températures, pressures, and other reaction conditions may be readily selected by one of ordinary skill in the art. Spécifie procedures are provided in the Synthetic Examples section. Typically, reaction progress may be monitored by thin layer chromatography (TLC) or LC-MS, if desired, and intermediates and products may be purified by chromatography on silica gel and/or by recrystallization.

The examples which follow are illustrative and, as recognized by one skilled in the art, particular reagents or conditions could be modified as needed for individual compounds without undue expérimentation. Starting materials and intermediates used, in the Schemes below, are either commercially available or easily prepared from commercially available materials by those skilled in the art.

The compounds of Formula (I) may be synthesized according to Scheme 1 : <\Υ '~

Scheme 1

As illustrated in scheme 1, reaction of a compound of formula II with a boronic acid or the corresponding boronic acid ester shown in the above scheme, in a suitable solvent, in the presence of a suitable a suitable catalyst, provides a compound of formula (I). Ra and Rb are hydrogen or Ra and Rb together with the oxygen atoms to which they are attached form a 5-6 membered ring optionally substituted with 2-4 methyl groups.

Altematively, reaction of a compound of formula II with a diborane, under standard reaction conditions, provides a compound of formula III. Coupling the intermediate of formula 111 with a halide or triflate R³X, in a suitable solvent, in the presence of a suitable catalyst, provides a compound of formula (I). X is chloro,bromo, triflate, or iodo.

The compounds of Formula (I) may be prepared according to Scheme 2: Y

R⁵COCI

or

R⁵COOH

I

Scheme 2

As illustrated in scheme 2, reaction of a compound of formula IV with an acid chloride

R⁵COCl, in a suitable solvent, in the presence of a suitable base, provides a compound of formula (I).

Altematively, reaction of a compound of formula IV with an acid R⁵COOH, in a suitable solvent, în the presence of carbonyl diimidazole, or other suitable amide coupling reagent, provides a compound of formula (I).

Addîtionally, reaction of a compound of formula IV with trichloromethyl anhydride, provides a compound of formula (I) wherin R⁵ is trichloromethyl. The trichloromethyl group may be further converted to another group by using procedures known to one skilled în the art.

The intermediate of formula II may be synthesized as outlined in Scheme 3:

X-(CH₂)_n-X _V| base

R⁵COCl or R⁵COOH

Scheme 3

As illustrated in scheme 3, reaction of a nitrile of formula V with a dihalide VI wherein one of the carbon atoms in the alkyl chain may be optionally substituted with O, S or N, in a suitable solvent, in the presence of a suitable base such as sodium hydride, provides a substituted nitrile of formula VII. R¹ and R² together with the carbon atom to which they are attached form a CX carbocyclic or heterocyclic ring. X is chloro, bromo, or iodo. Reaction of the compound of formula VII with hydroxylamine, under standard reaction conditions, provides a compound of formula VIII. Reaction of the compound of formula VIII with an acid chloride R⁵COC1, in a suitable solvent, in the presence of a suitable base, provides a compound of formula II. Altematively, reaction of a compound of formula VIII with an acid R⁵COOH, in a suitable solvent, in the presence of carbonyi diimidazole, or other suitable amide coupling reagent, provides a compound of formula II.

Intermediate of formula VIII may also be converted to the trichloromethyl intermediate of formula IX by reacting it with a reagent such as trichloromethyl anhydride, under standard conditions. Reaction ofthe intermediate IX with R⁵H when R^SH contains a primary or secondary amino group, in a suitable solvent provides an intermediate of formula il

The intermediate of formula IV may be synthesized according to Scheme 4:

As illustrated above in scheme 4, reaction of a nitrile of formula VII with a boronic acid or the corresponding boronic acid ester shown in the above scheme, in a suitable solvent, in the presence of a suitable catalyst, provides a compound of formula X. Ra and Rb are hydrogen or Ra and Rb together with the oxygen atoms to which they are attached form a 5-6 membered ring optionally substituted with 2-4 methyl groups. Altematively, coupling may also be achieved by reacting R³-(Sn (CHQ Y with a starting material of formula VII, in the presence of a suitable catalyst, to provide a compound of formula X. Reaction of a compound of formula X with hydroxylamine, under standard reaction conditions, provides a compound of formula IV.

The nitrile intermediate of formula XIII may be synthesized according to Scheme 5:

R¹\ R²

Base

Br

XI

XIII

Scheme S

As illustrated above in scheme 5, reaction of a dihalide of formula XI with a nitrile of formula XII, under standard reaction conditions, in the presence of a suitable base, provides an intermediate of formula XIII. The intermediate of formula XIII may be converted to a compound of formula (IA) by the sequence of reactions shown in scheme 3.

Compounds of formula (IA) may be synthesized using any of the above schemes by using the appropriate staring materials and reagents.

Further modification ofthe initial product of Formula (I) and (IA), by methods known in the art, such as alkylation of heterocycles, and illustrated in the Examples below, may be used to préparé addîtional compounds of this invention.

SYNTHETIC EXAMPLES

Préparation of Intermediates

Nitrile Intermediates

Synthesis of l-(6-chloro-pvridin-3-vD-cyclobutanecarbonitrile (Intermediate 1-1.1) γ

To a solution of compound RI (65 g, 0.426 mol) in DMF (500 mL) at 0 “C is added NaH (60% in oil suspension, 37.5g, 0.937 mol) portion-wise over 20 minutes. The mixture is stirred for a further 20 minutes and R2 (44.1 mL, 0.435 mol) is added. The réaction mixture is warmed to room température and stirring is continued for l hour. The reaction is then quenched by the addition of water (200 mL) and concentrated în vacuo. The residue is partitioned between ethyl acetate (EtOAc) and saturated aqueous NaHCO; and the phases are separated. The organic phase is dried over Na₂SÛ4, filtered and concentrated in vacuo. The residue is purified by flash column chromatography (SiO₂,

20-60% ethyl acetate/heptane) to yield intermediate I-l.l (63 g); m/z 193 [M+l].

The following intermediate is synthesized in a similar fashion from the appropriate reagents:

Intermediate	Structure	m/z [M+H]
1-1.2	XX CK N	223

Synthesis of l-(5-Bromo-Dvridin-2-vO-cvclobutanecarbonitrile (Intermediate 1-1.3)

N

R4

R6

R5 (1.41 mL, 10.0 mmol) is added to THF (20 mL) and the resultîng mixture is cooled to -10 °C. To the resultîng mixture is added R6 (1.6M in hexanes, 6.25 mL, 10.0 mmol) and the reaction is stirred for 30 minutes. The mixture is then cooled to -78 ^rtC and R4 (811 mg, 10.0 mmol) îs then added and the reaction is stirred at -78 °C for 45 minutes. At this time a mixture of R3 (1.90 g, 8.02 mmol) in THF (5 mL) is added and the mixture is allowed to warm to room température and stirred overnight. The resulting mixture îs concentrated and the residue is partitîoned between water and ethyl acetate. The phases are separated and the aqueous phase is extracted with ethyl acetate. The organic phases are combined, washed with brine, dried over Na₂SO4, and concentrated. The crude residue is purified by flash chromatography (SiO₂, ethyl acetate/heptane gradient) to yield întermediate 1-1.3 (1.10 g); m/z 237.2, 239.1 [M+H for⁷⁹Br and ^R1Br].

The following întermediate is synthesized in a similar fashion from the appropriate reagents:

Intermediate	Structure	m/z [M+H]
1-1.4	Br	267

Synthesis of l-[5-(2-Aniino-Dyrimidin-5-yl)-pyridin-2-vl|-cvclobutanecarbonitrile (Intermediate 1-1.5)

R7 (553 mg, 2.00 mmol) and palladium (Ii) acetate-dicyclohexylphenylphosphine PE fibers (FibreCat 1007, 167 mg, 0.100 mmol) are combined in a microwave vial. 1-1.3 (474 mg, 2.50 mmol), THF (10.0 mL), and 2M aqueous Na₂CO₃ (4.00 mL) are then added and the reaction is heated in the micro wave at 120 °C for 45 minutes. The resulting mixture îs diluted with water and ethyl acetate and filtered. The organic phase is collected, washed with brine, dried over NaiSOi, and concentrated. The crude residue ' is purified by flash chromatography (SiCl·, ethyl acetate/heptane gradient) to yield intermediate I-l .5 (300 mg); m/z 252.2 [M+H].

Synthesis of l-[6-(2-amino-pyrimidin-5-vl)-pvridin-3-yl]-cvclobutanecarbonitrite (Intermediate 1-1.6)

(THF)

Pd(PPh₃)₄sat’d Na₂CO₃

To a suspension of 1-1.1 (3.00 g, 15.6 mmol) and R8 (4.13 g, 18.7 mmol) in THF (30 mL) is added Pd(PPh₃)₄ (1.8 g, 1.56 mmol) and saturated aqueous Na₂CO₃ (10 mL). The mixture is heated to reflux overnight. The reaction mixture is concentrated in vacuo and 10 purified by flash chromatography (S1O2, 0-3% methanol/CHîCL) to afford the title intermediate 1-1.6 (3.7 g); m/z 252 [M+H].

Intermediate	Structure	m/z [M+H]
1-1.7	W H	279.9

Synthesis of l-[6-(5-Methvlamino-pvrazin-2-vl)-pyridin-3-vllcyclobutanecarbonitrile (Intermediate I-L8)

R76 ^R64

(THF)

Pd(PPh₃)₄

R76 (500 mg, 2.66 mmol) îs treated with R64 (0.96 g, 2.93 mmol) and THF (12 mL) and the resulting mixture is degassed with argon and treated with Pd(PPhj)4 (307 mg, 0.266 mmol mmol). The mixture is heated at 95 °C for 2 hours at which time it is treated with I5 l.l (0.61 g, 3.19 mmol) and Pd(PPh₃)₄ (307 mg, 0.266 mmol mmol) again and heated at °C overnight. The reaction mixture is concentrated in vacuo and purified by flash chromatography (S1O2, 0-8% methanol/CH₂Cl2) to afford the title intermediate 1-1.8 (1.00 g); m/z 267.2 [M+H].The following intermediates are synthesized in a similar fashion from the appropriate reagents:

Intermediate	Structure	m/z [M+H]
1-1.9	ΙΓ h₂n n	266.4
1-1.10	H T X N. X Y ΙΓ h₂n n	252.4

Carboxamidine Intermediate

Synthesis of l-(6-chloro-i)vridin-3-vl)- V-hvdroxv-cvclobutanecarboxamidine (Intermediate 1-2.1)

1-1.1 h₂n-oh

R9

To a solution of I-l.l (30 g, 0.156 mol) in éthanol (400 mL) is added R9 (50% aqueous solution, 95.4 mL, 1.56 mol). The reaction mixture is stirred at 80 °C for 18 h. The reaction is cooled to room température, the éthanol is evaporated in vacuo, and the concentrated mixture is extracted with CH2CI2 (DCM). The combined organics are dried with NioSO.j. filtered and concentrated in vacuo to give the title intermediate I-2.1 (29.8 g); m/z 226 [M+H].

The following intermediates are synthesized in a similar fashion from the appropriate reagents:

Intermediate	Structure	m/z [M+H]
1-2.2	.0 X JI cr N OH	256
1-2.3	.0 bAⁿ %h	256

ÎO Synthesis of l-l6-(2-amino-pvrimidin-5-vl)-pvridin-3-vl|-7V-hvdroxycyclobutanecarboxamidine (Intermediate 1-3.1)

To a solution of 1-1.6 (8.85 g, 35.2 mmol) in éthanol (40 mL) is added R9 (50% aqueous solution, 20 mL, 326 mmol). The reaction mixture is stirred at reflux for 18 hours. The 15 reaction mixture is cooled to room température, the éthanol is evaporated in vacuo, and the precipitate is collected via filtration to yield the title intermediate 1-3.1 (8.80 g); m/z .

285 [M+H].

Intermediate	Structure	m/z [M+H]
i-3.2	_nUv'n %_h Λ J h₂n n	285.2
1-3.3	N N OH A J HN N 1	299.2
1-3.4	j-yA N'oh HN A 1	299.2
1-3.5	^J>Çnh₂ [fAU A h₂n n^	299.9
1-3.6	At ï^NH2ij^nJ ^ohh₂n n	285.1

Pyridyl Halide Intermediates

Synthesis of 2-Chloro-5-ll-(5-pvridin-3-vl-l,2,4-oxadiazol-3-vO-cvclobutyll-pyridine (Intermediate

nh₂

OH +

RIO (356 mg, 2.00 mmol) is treated with pyridine (2 mL) and I-2.1 (500 mg, 1.33 mmol) and the resulting mixture is heated at 110 °C until the starting material is consumed. The reaction is cooled to room température and the solvent is removed in vacuo. The residue is diluted with ethyl acetate and saturated aqueous NaHCCL and the phases are separated. The aqueous phase is extracted twice more with ethyl acetate and the combined organics are washed twice with saturated aqueous Nal l CO; and once with brine. The organics are collected, dried over Na2SO₄, filtered, and the solvent is removed in vacuo to give 1-4.1 (285 mg); m/z 313 [M+H].

Synthesis of 2-Ch lor o-5- [ 1-15-(1 7/-pvrazol-4-y 1)-1.2,4-oxadiazol-3-yl 1-cyclobutyl ]pyridine (Intermediate 1-4.2)

1-2.1 +

H N-N

R11

Cl, s=o

Cl'

R12

RI 1 (156 mg, 1.40 mmol) is treated with pyridine (10.0 mL) and R12 (116 pL, 1.60 mmol) and the resulting mixture is stirred for 30 minutes. 1-2.1 (300 mg, 1.33 mmol) is then added and the reaction is stirred at 110 °C for 18 hours. The resulting mixture is cooled to room température and the solvent is removed in vacuo. The residue is partitioned between CH2CI2 and saturated aqueous NaHCOj and the phases are separated. The organic phase is dried over Na₂SO₄, filtered, and the solvent is removed in vacuo to give 1-4.2 (187 mg); m/z 301.9 [M+H].

Synthesis of 2-(4-(3-1 l-(6-chloro-pvridin-3-yl)-cvclobntyll-l,2_Î4-oxadiazol-5-vUpyrazol-l-vl)-/V-methyl-acetamide (Intermediate 1-4.3) 0/^

Ι-4.2 (NMP) '4.3

1-4.2 (23 wt% with NMP, 691 mg, 0.527 mmol) îs treated with DMF (4.0 mL), R13 (84.1 mg, 0.553 mmol), and K.2CO3 (109 mg, 0.790 mmol) and the reaction is heated at 80 °C for 17 hours at which time R13 (8 mg, 0.0.026 mmol) and K₂CO₃ (3.6 mg, 0.026 mmol) are again added and the reaction is heated at 80 °C for 16 hours. The solvent is removed in vacuo and the residue is partitîoned between water and ethyl acetate. The layers are separated and the aqueous is again extracted with ethyl acetate. The combined organic phases are washed with brine and the solvent is removed in vacuo to give 1-4.3 (195 mg); m/z 373.3 [M+H],

Synthesis of (4-13-1 l-(6-chloro-pvridin-3-vl)-cvclobutyll-L2.4-oxadiazol-5-vlÎpyrazol-l-yl)-acetic acid ethyl ester (Intermediate 1-4.4)

1-4.2

R14

I-4.4

1-4.4 is prepared according to the method for 1-4.3 using RI 5 in place of R13 to give 1-4.4 (259 mg); m/z 388 [M+H].

Synthesis of 2-(4-{3-|l-(6-chloro-pvridin-3-vl)-cvclobutvll-L2,4-oxadiazol-5-yllpvrazol-l-vl)-V,A-diinethyl-acetaniide (Intermediate 1-4.5)

I-4.4

H-Ci

R15

I /Al_s

R16

RI5 (164 mg, 2.00 mmol) is treated with toluene (6 mL) and RJ 6 (2M in toluene, 0.280 mL, 2.00 mmol) and the resulting mixture is stirred for 30 minutes. 1-4.4 (259 mg, 0.669 mmol) is then added and the mixture is stirred at 100 °C for 2 hours. The reaction is cooied to room température and water is added. The layers are separated and the organics are dried with Na₂SC>4, filtered, and the solvent removed in vacuo to provide I4.5 (200 mg); m/z 387 [M+H].

Synthesis of 2-chloro-5-14-(5-pvridin-3-vl-1.2_<4-oxadiazol-3-yh-tetrahvdro-pyran-4yll-pyridine (Intermediate 1-4.6)

1-2.2

R17

I-4.6

1-2.2 (500 mg, 1.96 mmol) is treated with pyridine (5 mL), and R17 (522 mg, 2.93 mmol) and heated at 110 °C for 1 hour. The reaction is cooied to room température and the solvent is removed in vacuo. The residue is diluted with ethyl acetate and saturated aqueous NaHCO₃ and the phases are separated. The aqueous phase is extracted twice more with ethyl acetate and the combined organics are washed with saturated NaHCO₃twice, then brine. The organic phase is collected, dried with Na₂SO4, filtered, and the solvent removed in vacuo to provide 1-4.6 (525 mg); m/z 343 [M+H].

The following intermediate are synthesîzed in a similar fashion from the appropriate reagents:

Intermediate

Structure

m/z [M+H]

A'·

Synthesis of 2-(4-i3-H-(6-chloro-pvridin-3-vh-cvclobutyl|-l,2.4-oxadiazol-5-vlîpyrazol-l-vl)-2-methvl-propan-l-ol (Intermediate 1-4.10)

R18

Li’ BH₄

R20

Step 2

Step 1: Synthesis of2-(4-{3-[l-(6-chloro-pyridin-3-yl)-cyclobutyl]-l,2,4-oxadiazol-5yl}-pyrazol-l-yl)-2-methyl-propionic acid methyl ester (R 19)

R19 is prepared according to the method for 1-4.6 using RI8 in place of R13; m/z 402 [M+H].

Step 2: Synthesis of 2-(4-{3-[l-(6-chloro-pyridin-3-yl)-cyclobutyl]-l,2,4-oxadiazol-5yl} -pyrazol-1 -yl)-2-methyl-propan-1 -ol (1-4.10)

R19 (83.1 mg, 0.207 mmol) is treated with THF (2.0 mL) and cooled to 0 °C. R20 (9.0 mg, 0.41 mmol) is then added and the reaction is warmed to room température and stirred for 2 hours at which time the solvent is removed in vacuo. The residue is partitioned between saturated aqueous NaHCO₃ and ethyl acetate and the organic layer is collected, dried with Na₂SO4, filtered, and the solvent removed in vacuo to afford I-4.10 (78 mg);

m/z 374 [M+H].

Synthesis of 2-(4-(3-1 l-(6-clili)ro-pvridin-3-vl)-cvclobutyl|-L2.4-oxadiazol-5-vllpvrazol-l-vlÎ-2-methvl-propan-l-ol (Intermediate 1-4.Il)

Step

OH

Li* BH₄

R20

Step 2

1-4.11 is prepared according to the procedure for 1-4.10 using the appropriate reagents;

m/z 360 [M+H].

Synthesis of (5-f3-|l-(6-Chloro-pvridin-3-vl)-cvclobutvll-l,2,4-oxadiazol-5-vIÎpvrazin-2-vl)-(2-niethoxv-ethyl)-amine (Intermediate 1-4.12)

R23 R24 R25

R26

R27

(HATU)

Step 1 : synthesis of 5-chloro-pyrazine-2-carboxylic acid methyl ester (R24)

R23 (2.00 g, 14.3 mmol) is treated with R12 (10.0 mL) and to the resulting mixture is added DMF (0.1 mL) dropwise. The reaction mixture is then heated at reflux for 4 hours.

The solvent is removed in vacuo and the residue is treated with méthanol ( 10.0 mL) and pyridine ( l .39 mL, 17.1 mmol) and the resulting mixture is stirred overnight. The solvent is removed in vacuo and the residue is purified by flash chromatography (SÎO₂, 20% ethyl acetate/cyclohexane) to give R24 (L 12 g); m/z 173 [M+H].

Step 2; synthesis of 5-(2-methoxy-ethylamino)-pyrazine-2-carboxylic acid methyl ester (R26)

R24 (200 mg, L16 mmol) îs treated with dimethyl suifoxide (DMSO) (4.00 mL) and R25 (I5l mL, 1.74 mmol) and the resulting mixture is heated at 80 °C for 2 hours. The mixture is diluted with water (5 mL) and acidified to approximately pH 2 with 2M aqueous HCl. The resulting mixture is extracted 3 times with ethyl acetate and the combined organic phases are washed with saturated brine, collected, dried over MgSO₄, filtered, and the solvent is removed in vacuo. The crude residue is purified by flash chromatography (SÎO₂, 90% ethyl acetate/cyclohexane) to give R26 (143 mg); m/z 212 [M+H],

Step 3: synthesis of 5-(2-methoxy-ethylamîno)-pyrazine-2-carboxylîc acid (R22)

R26 (143 mg, 0.701 mmol) is treated with THF (1.50 mL), water (1.50 mL) and lithium hydroxide (25.2 mg, 1.05 mmol) and the resulting mixture is stirred at room température overnight. The solvent is removed in vacuo to give crude R27 (138 mg); m/z 196 [M+H],

Step 4: synthesis of(5-[3-[l-(6-Chloro-pyridin-3-yl)-cyclobutyl]-l,2,4-oxadiazol-5-yl}pyrazin-2-yi)-(2-methoxy-ethyl)-amine (Intermediate 1-4.12)

R27 (138 mg, 0.700 mmol) is treated with DMF (7.00 mL), HATU (266 mg, 0.700 mmol), and triethylamine (TEA) (0.10 mL, 0.700 mmol) and the resulting mixture is stirred for 5 minutes at which time 1-2.1 (158 mg, 0.700 mmol) is added and the reaction is stirred at 90 °C overnight. The solvent is removed in vacuo and the resulting residue is partitioned between ethyl acetate and saturated aqueous NaHCO₃ and the layers are separated. The aqueous phase is extracted twice more with ethyl acetate and the combined organics are washed with water, brine, collected, dried over MgSO₄, filtered, and the solvent is removed in vacuo. The crude residue is purified by flash chromatography (SiO₂, 50% ethyl acetate/cyclohexane) to give 1-4.12 (181 mg); m/z 387 [M+H].

Synthesis of 2-Chloro-5-(l-|5-(l-oxetan-3-yl-l ll-pvrazol-4-xl)-U.2,4|oxadiazol-3-yl|cvclobutvIÎ-pyridine (Intermediate 4.13)

R38

1-4.13 is prepared according to the method for 1-4.3 using R38 in place of RI3 to afford the title compound (500 mg).

Synthesis of 1-(4-(3-11-(6-Chloro-pvridin-3-yI)-cyclobiitvl|-|1.2.4|oxadiazol-5-yliPvrazol-l-yl)-2-methyl-propan-2-ol (Intermediate 1-4.14)

1-4.2

R37

1-4.14 is prepared according to the method for 1-4.3 using R37 in place of R13 to afford the title compound (600 mg).

Synthesis of 5-(5-ll-|5-(lH-Pvrazol-4-vl)-|1.2,41oxadiazol-3-vll-cyclobutvl)-pvridin15 2-vi)-pyrazin-2-ylamine (Intermediate 1-5,1)

I-5.1 is prepared according to method 10 to afford the title compound (470 mg).

Intermediate	Structure	m/z [M+H]
1-5.2	T\|i^No ii^{N N} x H₂N N n^^NH	375.2
1-5.3	rrv^No . X X h N N < ,N H N H	374.9

Method 1:

Synthesis of 5-(5-[l-15-(6-chloroDvridin-3-vl)-l,2,4-oxadiazol-3-yltcvclobutvlIpvridin-2-vl)-pyrimidin-2-amine (Example 99, Table 1)

0 II	Ο 11 \Z Z?
★ ^H0 τΊ	(CDD

R28

R28 (5.41 g, 19.0 mmol) is treated with THF (25 mL) and CDI (3.09 g, 19.0 mmol) and heated at 50 °C for 20 minutes at which time 1-3.1 is added and the reaction is refluxed overnight. The reaction is cooled to room température and the resulting precipitate is collected by filtration and recrystallized from acetonitrile to afford the title compound (5.68 g); m/z 406.2 [M+H],

Examples in table 1 listed with method 1 are synthesized in a similar fashion. Example

32 uses NMP as solvent and the second stage is heated at 100 °C overnight. Example 57 uses DMF as solvent and is heated at 100 °C for 3 hours. Examples 81 and 83 use NMP V-Z” as solvent, the first stage is run at room température, and the second stage is at 70 °C for 30 minutes. Examples 88 and 94 use NMP as solvent and the second stage is run at 80 °C for 2 hours. Example 120 uses NMP as the solvent and the second stage is run at 130 °C for 2 hours. Example 132 uses dimethylacetamide as solvent and is heated at 140 °C for 55 minutes.

Method 2:

Synthesis of 5-15-(1 -{5-|6-(propan-2-vlamino)pyridin-3-yl|-l,2,4-oxadiazoI-3-ylicvclobut¥l)pvridin-2-yllpvrimidin-2-amine (Example 114, Table 1)

Example 99 (50 mg, 0.123 mmol) is treated with THF (2 mL) and R29 (0.5 mL) and the resulting mixture is heated at 100 °C for 2 hours. The solvent is removed in vacuo and the resulting residue is suspended in water. The precipitate is collected by filtration and recrystallized from acetonitrile/methanol to afford the title compound (50 mg); m/z 429.6 [M+H],

Examples in table 1 listed with method 2 are synthesized in a similar fashion. Examples 43, 45, and 47-49 are run at 60 °C overnight; example 125 is run in NMP at 100 °C for 3 days with 3 équivalents of TEA added; example 21 is run în THF at 100 °C for 3 days; example 111 is run at 100 °C for 24 hours; examples 50 and 52 are run in NMP at 100 °C overnight; examples 34 and 116-118 are run neat at 80 °C for 2 hours; example i 12 is run neat at 100 °C for 2 days; example 13 is run in NMP at 100 °C for 6 hours with 3 équivalents of TEA added; example 51 is run in NMP at 100 °C overnight with 3 équivalents of TEA added; example 2 is run in NMP at 100 °C for 6 hours.

Method 3:

Synthesis of 3-Î4-|5-(3-il-|6-(2-aminopvrimidin-5-vl)pyridin-3-yllcvclobutylÎ-l,2,4oxadiazol-5-yl)pvridin-2-vl]piperazin-l-ylÎpropanoic acid (Example 53, Table 1)

Ex. 47

Ex. 53

Example 47 (400 mg, 0.720 mmol) îs treated with THF (2 mL), methanol (2 mL) and 5M aqueous NaOH (2 mL) and stirred overnight. The solvent is removed in vacuo and the resulting residue is acidified with concentrated aqueous HCl and the solvents are again removed in vacuo. The residue is purified b y reverse-phase préparative HPLC to afford the title compound (162 mg); m/z 528.2 [M+H].

Method 4:

Synthesis of methyl (27?)-l-l5-(3-il-l6-(2-amÎnopvrimidin-5-vl)pvridin-3vl|cyclobutvll-l,2.4-oxadiazol-5-vl)pvridin-2-vl|piperazine-2-carboxylate (Example

38, Table 1)

R30

Example 99 ( 120 mg, 0.296 mmol) is treated with R30 (361 mg, 1.48 mmol) and NMP (0.150 mL) and heated at 80 °C for 48 hours. The resulting mixture is cooled to room température and treated with 4N HCl in 1,4-dioxane (1.50 mL) and stirred for 1.5 hours. The resulting mixture is purified by reverse-phase préparative HPLC (C-l 8 silica, 1030% acetonitrile/water/0.1% trifluoroacetic acid over 20 minutes) to afford the title compound as a trifluoroacetic acid sait (110 mg), m/z 514.8 [M+H].

Examples in table 1 listed with method 4 are synthesized in a similar fashion.

Method 5:

Synthesis of (25)-4-|5-(3-Îl-16-(2-aminopvrimidin-5-vhpyridin-3-vllcvclobutvlll,2_Î4-oxadiazol-5-vl)pyridin-2-yllpiperazine-2-carboxylic acid (Example 41, Table 1)

Example 39 (135 mg, 0.215 mmol) is treated with methanol (l.00 mL) and 5M aqueous NaOH (l.OO mL) and the resulting mixture is heated at 70 °C for 2 hours. The mixture is then cooled to room température and filtered to afford the title compound (35 mg); m/z

500.7 [M+H].

Examples in table l listed with method 5 are synthesized in a similar fashion. Example 16 used sodium methoxîde in place of NaOH with water as a co-solvent.

Method 6:

Synthesis of methyl 1-15-(3-( l-|6-(2-aminopvrimidin-5-vbpvridin-3-yllcvclobutvl}1.2.4-oxadiazol-5-vnpvridin-2-vl]-L-prolinate (Example 36. Table 1) and 1-15-(3-(1[6-(2-aminopvrimidin-5-v])pvridin-3-y]lcvclobutyl}-l,2,4-oxadiazol-5-vl)pyridin-2-

Ex. 99

R31

Example 99 (100 mg, 0.246 mmol) is treated with R3 1 (204 mg, 1.23 mmol), NMP (0.5 mL), and TEA (0.5 mL) and the resulting mixture is heated at 80 °C for 2 hours. The crude mixture containing both title products îs directly purified by reverse-phase ά/ préparative HPLC (C-18 silica, 10-50% acetonitrile/water/0.1% trifluoroacetic acid over minutes) to afford the title compounds example 35 (24 mg), m/z 499.8 [M+H] and example 36 (24 mg), m/z 512.8 [M+H].

Method 7:

Synthesis of 5-|5-(l-i5-|6-(lH-imidazol-l-vl)pvridin-3-yll-l,2,4-oxadiazol-3vllcyclobutyl)Pvritiin-2-vl|pvrimidin-2-amine (Example 31. Table 1)

\

R28 (1.21 g, 7.74 mmol) is treated with N MP (7.00 mL) and CDI (1.25 g, 7.74 mmol) and heated at 50 °C for 20 minutes. To this mixture is then added 1-3.1 (2.00 g, 7.03 mmol) and the resulting mixture is heated at 130 °C for 2 hours. The mixture is cooied to room température and treated with water (70 mL) and the solid is collected by filtration. This crude mixture is purified by flash chromatography (SiO₂, 0-10% methanol/CH₂Ci₂) to afford the title compound (245 mg); m/z 438.6 [M+H],

Method 8:

Synthesis of 5-i5-(l-i5-i5-(4-methvlpiperazin-l-vl)pyrazin-2-vl|-l,2.4-oxadiazol-3vllcvclobutvlÎPvridin-2-vl|pvrimidin-2-amine (Example 61, Table I)

Step l: synthesis of 5-(5-( l-[5-(5-imidazol-l-yI-pyrazin-2-yI)-1,2,4-oxadiazoI-3-yl]cyclobutyl}-pyridin-2-yl)-pyrimidin-2-ylamine (R33).

R32 (300 mg, 1,89 mmol) is treated with DMF (5,00 mL) and CDI (306 mg, 1.89 mmol) and stirred at 50 °C for 20 minutes. To this mixture is added 1-3.1 (488 mg, 1.72 mmol) and the resulting mixture is heated at 110 °C for 2 hours. The solvent is removed in vacuo and the resulting residue is partitioned between ethyl acetate and saturated aqueous NaHCO₃. The phases are separated and the resulting precipitate in the aqueous phase is collected by filtration. The organic phase îs dried over Na₂SO₄, filtered, and the solvent is removed in vacuo. The collected solids from the aqueous layer and the residue from the organics are combined to afford R33 (384 mg); m/z 439.0 [M+H],

Step 2: synthesis of 5-[5-(l-(5-[5-(4-methylpiperazin-l-yl)pyrazin-2-yl]-l,2,4-oxadiazol3-yl}cyclobutyl)pyridin-2-yl]pyrimidin-2-amine (example 61).

R33 (284 mg, 0.389 mmol) is treated with DMSO (1.00 mL), K₂CO₃ (53.7 mg, 0,389 mmol), and R34 (64.7 pL, 0.583 mmol) and the mixture is heated at 80 °C for 1 hour. The mixture is cooled to room température and diluted with water (3 mL) and rendered basic (pH >9) by addition of 2M aqueous NaOH. The resulting mixture is extracted 3 times with CH₂C1₂ and the combined organic phases are washed with brine, dried over Na₂SO4, filtered, and the solvent is removed in vacuo. This crude mixture is purified by flash chromatography (SiO₂, 0-10% methanol/CH₂Cl₂) to afford the title compound (90.8 mg); m/z 470.2 [M+H].

Method 9:

Synthesis of 5-[5-(Î-f5-[6-(methvlsulfonvl)pvridin-3-yl|-L2,4-oxadiazol-3vl}cvclobutvl)pvridin-2-vllpyrimidin-2-amine Example 119, Table 1)

R35

Ex. 119

Ex. 99

Example 99 (50.0 mg, 0.123 mmol) is treated with NMP (0.75 mL) and R35 (148 mg) and the resulting mixture is heated at 80 °C for 2 hours. The mixture is cooled to room température and filtered. The filtrate is purifîed by reverse-phase HPLC (15-65% acetonitrile/water/0.1% trifluoroacetic acid) to afford the title compound (23.0 mg); m/z 450.2 [M+H].

Method 10:

Synthesis of 5-(5-]l-[5-(l-methvl-lH-pyrazol-4-vl)-l,2,4-oxadiazol-3vllcvclobutvlÎpvridin-2-vl)pyrimidin-2-amine (Example 102. Table 1)

o

R36

Ex. 102

R.36 (53.2 mg, 0.422 mmol) is treated with NMP ( l .50 mL), diisopropylethylamine (DIEA) (0.08 mL, 0.42 mmol) and HATU (161 mg, 0.422 mmol) and stirred for 15 minutes. To this mixture is added 1-3.1 (100 mg, 0.352 mmol) and the resulting mixture is heated at 100 °C for 4 hours. The reaction mixture is directly purifîed by reverse-phase HPLC ( 10 to 35% acetonitrile/water/0.1% trifluoroacetic acid) to afford the title compound (46.0 mg); m/z 375.2 [M+H].

Examples in table 1 listed with method 10 are synthesized in a similar fashion. Example is heated at 130 °C for 6 hours. Examples 4, 123-124, and 127 use TEA in place of

DIEA and are heated at 100 °C for 16 hours. Examples 5-7, 11, 17, 19, 93, 96-98, 101, and 129-130 use TEA in place of DIEA and are heated at 80 °C overnight. Example 14 uses TEA în place of DIEA and is heated at 100 °C for 1 hour. Example 20 uses TEA in place of DIEA and is heated at 100 °C for 2 hours. Examples 23-26 use TEA in place in

DMF and are heated at 110 °C for 2 hours. Example 27 uses TEA in place of DIEA in DMF and is heated at 80 °C overnight. Example 28 uses TEA in place of DIEA and is heated at 110 °C overnight. Example 74 uses no base and is heated at 80 °C for 2 hours. Example 86usesTEA in place of DIEA in DMF and is heated at 120 °C for 1 hour.

Examples 91 and 92 use TEA in place of DIEA in DMF and is heated at 80 °C for 2 hours. Example 100 and 109 use TEA in place of DIEA and is heated at 80 °C for 2 hours. Example 104 is heated at 130 °C for 2 hours. Examples 75, 77-80, and 131 use

TEA in place of DIE A in DMF and are stirred at room température overnight prior to heating at 110 °C for 4 hours. Example 133 uses dimethylacetamîde as solvent and is heated at 100 °C for 1.5 hours. Example 134 uses dioxane as solvent and is heated at 90 °C for 16 hours, then 100 °C for 8 hours. Example 135 uses dimethylacetamîde as solvent and is heated first at 100 °C for 1.5 hours, then 45 °C for 16 hours, then 90 °C for 5 hours.

Method 11 :

Synthesis of l-r4-(3-{l-16-(2-aminopvrimidin-5-v0pvridin-3-vllevclobutvlÎ-l,2,4oxadiazol-5-vl)-lH-pyrazol-l-yll-2-methvlpropan-2-ol (Example 54, Table 1)

Example 90 (5.00 g, 13.9 mmol) is treated with R37 (4.00 g, 36.8 mmol), K₂CO₂ (2.88 g, 20.8 mmol) and DMF (50 mL) and the resulting mixture is heated at 80 °C for 60 hours. The reaction mixture îs diluted with ethyl acetate and washed with water and brine. The organic phase is dried over Na₂SO4, filtered, and the solvent is removed in vacuo. This crude mixture is purified by flash chromatography (SÎO₂, 0-5% 2M NH₃ in methanol/CLLCb) to afford the title compound (2.58 g); m/z 433.4 [M+H].

Examples in table 1 listed with method 11 are synthesized in a similar fashion. Examples 63-64, 67-68, and 171 are stirred at room température for 18 hours. Example 69 is stirred first at room température for 18 hours, then 65 °C for 18 hours. Example 70 is stirred at room température for 4 hours. Examples 170 and 173 are stirred at room température for 18 hours. Example 172 is stirred at 75 °C for 18 hours.

Method 12:

Synthesis of 5-15-(l-{5-ll-(oxetan-3-vn-lH-pyrazol-4-vll-l,2,4-oxadiazol-3vncvclobutvl)pvridin-2-vllpvrimidin-2-amine (Example 55, Table 1)

R38

Example 90 (500 mg, 1.39 mmol) is treated with R38 (510 mg, 2.77 mmol), K₃CO₃ (383 mg, 2.77 mmol) and DMF (8 mL) and the resulting mixture is heated at 50 °C for 18 hours. A second charge of R38 (510 mg, 2.77 mmol) is then added and the mixture Îs heated at 80 °C for 18 hours. The reaction mixture is diluted with ethyl acetate and washed with water and brine. The organic phase is dried over NaiSOi, filtered, and the solvent is removed in vacuo. The crude mixture is purified by flash chromatography (S1O2, 0-5% 2M NH3 in methanol/CFLCh) to give a residue which is recrystallized from acetonitrile to afford the title compound (265 mg); m/z 417.4 [M+H].

Examples in table 1 listed with method 12 are synthesized in a similar fashion. Example ! 76 uses a single treatment at 80 °C for 18 hours.

Method 13

Synthesis of 5-(5-11-15-(4-methyl-4H-l,2,4-triazol-3-vl)-l,2,4-oxadiazol-3vllcvclobutvl)pvridin-2-vl)pvrimidin-2-amine (Example 37, Table 1)

Example 120 (147 mg, 0.407 mmol) is treated with K.2CO3 (84.3 mg, 0.610 mmol), DMF (1.0 mL), and Mel (69.3 mg, 0.488 mmol) and the resulting mixture is stirred for 30 minutes. The mixture is purified directly by préparative reverse-phase HPLC (10-35% acetonitrile/water with 0.1% TFA) to afford the title compound (28.0 mg); m/z 376.6 [M+H].

Method 14:

Synthesis of 5-{5-|l-(5-Îl-[(methylsnlfonvnmethvll-lH-pyrazol-4-vU-1.2,4oxadiazol-3-vOcvclobutvl|pvridin-2-vllpvrimidin-2-amine (Example 71, Table 1)

'η Step 2 mCPBA

Ex. 71

Step l : synthesis of 5-(5- {l-[5-( 1 -methylsulfanylmethyl-l/7-pyrazol-4-yl)-1,2,4oxadiazol-3-yl]-cyclobutyl}-pyridin-2-yl)-pyrimidin-2-ylamine (R40).

R40 is synthesized according to method 11 at room température for 16 hours.

Step 2: synthesis of 5-{5-(1-(5-{l-[(methylsulfonyl)methyl]-lH-pyrazol-4-yI}-1,2,4oxadiazoi-3-y!)cyclobutyl]pyridin-2-yl}pyrimidin-2-amine (Example 71).

Crude R40 (120 mg, 0.285 mmol) is treated with CH2CI2 (2.0 mL) and metachloroperbenzoic acid (mCPBA) (155 mg, 0.628 mmol) and stirred for 3 hours. The resulting mixture is diluted with saturated aqueous NaHCO₃ and CH₂C1₂ and the phases are separated. The organic phase is dried over MgSO₄, filtered, and the solvent is removed in vacuo. The crude residue is purified by préparative reverse-phase HPLC (1050% acetonitrile/water with 0.1% TFA). The resulting residue îs partitioned between NaHCOî and CH2CI2 and the phases are separated. The organic phase is dried over MgSO₄, filtered, and the solvent is removed in vacuo to afford the title compound (6.0 mg); m/z 453.4 [M+H].

Method 15î

Synthesis of 5-[5-(1-ί5-[1-(όΐΠ»θί·οιη£ίΙιν1)-1Η-ρνΓ3ζο1-4-ν11-1,2,4-θΧ3άΪ3ζο1-3vl}cvclobutvl)pvridin-2-vllpyrimidin-2-amine (Example 66, Table 1)

Ο

R41

Example 90 (150 mg, 0.416 mmol) is treated with R41 (72.0 mg, 0.498 mmol), CS2CO3 (676 mg, 2.08 mmol), and DMF (4.0 mL) and the resulting mixture îs stirred at 60 °C for 24 hours. The resulting mixture is diluted with ethyl acetate and water and the phases are 5 separated. The organic phase is washed with brine, dried over Na₂SO₄, filtered, and the solvent is removed in vacuo. The crude residue is purified by flash chromatography (SiO₂, 0-8% 2M NH3 in methanol/CH₂Cl₂) to afford the title compound (42 mg); m/z

411.4 [M+H].

Method 16:

Synthesis of 2-14-(3-1 l-|6-(2-aminODvrimidin-5-vl)pvridin-3-vl|cvclobutvH-1.2.4oxadiazol-5-vl)-lH-pvrazol-l-vll-2-methylpropanoic acid (Example 65. Table 1)

Step 1: synthesis of2-[4-(3-{l-[6-(2-Amino-pyrimidin-5-yl)-pyridin-3-yl]-cyclobutyl}15 l,2,4-oxadiazol-5-yl)-pyrazol-l-yl]-2-methyl-propionic acid methyl ester (R43).

R43 is synthesized according to method 11 with stirring at room température for 72 hours (819 mg); m/z 461.4 [M+H]..

Step 2: synthesis of 2-[4-(3-{ l-[6-(2-aminopyrimidin-5-yl)pyridin-3-yl]cyclobutyl}- l,2,4-oxadiazol-5-yl)-lH-pyrazol-l-yl]-2-methylpropanoic acid (Example 65)

R43 (200 mg, 0.434 mmol) is treated with THF (2.0 mL), methanol (2.0 mL), and 2M NaOH (2.0 mL) and the resulting mixture is stirred at 50 °C for 16 hours. The resulting mixture is extracted with ethyl acetate four times, and the combined organic phases are dried over Na₂SO₄, filtered, and the solvent is removed in vacuo. The aqueous phase is concentrated and the resulting solids are extracted with methanol and the extracts combined with the organic phase residue. The combined crude residue is purified by préparative reverse-phase HPLC (153 mg); m/z 447.3 [M+H].

Method 17:

Synthesis of 2-15-(3-1 l-|6-(2-aminopvriinidin-5-vl)pvridin-3-vl|cvclobutyl 1-1,2,4oxadiazol-5-vl)pyridin-2-yHpropan-2-ol (Exampie 82, Table 1)

Example 81 (59.0 mg, 0.137 mmol) is treated with THF (2.0 mL) and R44 (1.4M in toluene:THF 3:1, 0.49 mL, 0.69 mmol) and the resulting mixture is stirred for 2 hours. The mixture is then partitioned between water and CH₂C1₂ and the phases are separated. The organic phase is washed with brine, dried over Na₂SÛ4, filtered, and the solvent is removed in vacuo. The resulting mixture is purified directly by préparative reverse-phase HPLC (25-75% acetonitrile/water with 0.1% TFA) to afford the title compound (6.0 mg); m/z [M+H].

Method 18:

Synthesis of 5-(5-] 1-15-(5-amino-l H-pyrazol-3-yl)-l,2,4-oxadiazol-3vUcvclobutvlÎPvridin-2-vl)pvriniidin-2-amine (Example 10. Table 1)

R46

Step l: synthesis of 5-(5-{ l-[5-(5-nitro-2H-pyrazol-3-yl)-l ,2,4-oxadiazol-3-yl]cyclobutyl}-pyridin-2-yl)-pyrimidin-2-ylamine (R46).

R46 is synthesized according to the procedure for method 10 heating for l hour (180 mg); m/z 406.6 [M+H].

Step 2: Synthesis of 5-(5-{l-[5-(5-amino-lH-pyrazol-3-yl)-l,2,4-oxadiazol-3yl]cyclobutyl}pyridin-2-yl)pyrimidin-2-amine (Example 10).

R46 ( 180 mg, 0.444 mmol) is treated with ammonium formate (280 mg, 4.44 mmol), palladium on carbon (10 wt% palladium, 50.0 mg, 0.047 mmol), and méthanol (8.0 mL) 10 and the resultîng mixture is heated at 65 °C for 3 hours. The mixture is cooled to room température, filtered through celite, and concentrated in vacuo and the residue is purified by flash chromatography (SiCb, 0-10% methanol/CHoCL). The resultîng residue is treated with acetonitrile and heated at 70 °C for 2 hours and then filtered to afford the title compound (10 mg); m/z 376.6 [M+H].

Method 19:

Synthesis of 5-15-(l-i5-|6-(piperazin-l-vDpyridin-3-yl[-L2.4-oxadiazol-3vl}cvclobutvl)pyridin-2-vllpvrimidin-2-amine (Example 3, table 1)

>0

Ex. 3 ο

Ex., X

Example l ( l i 5 mg, 0.207 mmol) îs treated with 4.0M HCl in dioxane and stirred for 6 hours. The resulting solid is collected by filtration and dried to afford the title compound as the hydrochloride sait (55.0 mg); m/z 456.7 [M+H].

Examples in table I listed with method 19 are synthesized in a similar fashion.

Method 20:

Synthesîs of 5-|5-(l-{5-|5-(piperazin-l-vl)pvrazin-2-vl|-l,2,4-oxadiazol-3vlÎcvclobutvlÎpvridin-2-vl|pvrimidin-2-amine (Example 60, Table 1)

Step l: synthesis of 2,3,5,6-tetrahydro-[l,2^,]bipyrazinyl-4,5'-dicarboxylic acid 4-iertbutyl ester 5'-methyl ester (R49).

R47 (646 mg, 3.47 mmol) is treated with R48 (598 mg, 3.49 mmol), TEA (580 pL, 4.16 mmol), and NMP (10.0 mL) and the mixture is heated at 60 °C for 30 minutes. The reaction is cooled to room température and poured into ice water and the resulting solid îs collected by filtration to afford R49 ( L03 g); m/z 323.1 [M+H].

Step 2: synthesis of 2,3,5,6-Tetrahydro-[l,2']bipyrazinyl-4,5'-dicarboxylic acid 4-lertbutyl ester (R50).

R49 (890 mg, 2.76 mmol) is treated with éthanol (25 mL) and 5N NaOH (2.76 mL, 13.8 mmol). The mixture is stirred for several minutes at which time water (approximately 10 mL) is added and the reaction is stirred for 24 hours. The resulting mixture is diluted with water, acidified with acetic acid., and extracted twice with CH2CI2. The combined organic phases are washed with brine, dried over MgSO₄, filtered, and the solvent is removed in vacuo to afford R50 (690 mg); m/z 309.4 [M+H]. x^X'''

Step 3: synthesis of 5'-(3-{l-[6-(2-amîno-pyrimidin-5-yl)-pyridin-3-yl]-cyclobutyl}- l,2,4-oxadiazoi-5-yl)-2,3,5,6-tetrahydro-l,2’-bipyrazinyl-4-carboxylic acid tert-butyl ester (R51 ).

R50 (690 mg, 2.24 mmol) is treated with THF (10.00 mL) and CDI (370.7 mg, 2.29 mmol) and stirred at 50 °C for 30 minutes. To this mixture is added 1-3.1 (600 mg, 2.11 mmol) and the resulting mixture îs heated at 80 °C for 3 hours. The mixture is cooled to room température, acetic acid (1.8 mL) îs added, and the mixture is heated at 80 °C for 16 hours. The resulting mixture is cooled to room température, diluted with water and ethyl acetate and the phases are separated. The aqueous phase is extracted twice with ethyl acetate and the combined organic phases are washed twice each with water and saturated aqueous NaHCOj, dried over X1gSO₄. filtered, and the solvent is removed in vacuo to afford R51 (970 mg).

Step 4: synthesis of 5-[5-(l-{5-[5-(piperazin-l-yl)pyrazin-2-yl]-l,2,4-oxadiazol-3yl}cyclobutyl)pyridin-2-yl]pyrimidin-2-amine (Example 60).

Methanol (10.0 mL) is cooled to -5 °C and treated with acetyl chloride ( 1.00 mL). To this mixture is added R51 (0.50 g, 0.90 mmol) and the resulting mixture is stirred for 16 hours. The resulting mixture is treated with 7N ammonia in methanol until basic by pH paper and concentrated in vacuo. The resulting solid îs treated with acetonitrile and diluted with water. The mixture is filtered and the filtrate is treated with saturated NaHCO₃ (3 mL) and the solid is collected by filtration to afford the title compound (90.00 mg). m/z 457.3 [M+H].

Method 21:

Synthesis of 5-(5-il-[5-(2-chloropyridin-3-vl)-l,2,4-oxadiazol-3vI|cvclobutvIlpvridin-2-vl)pyrimidin-2-amine (Example 84, Table 1)

Cl

O

H,N N h₂n n

1-3.1

R52

Ex. 84

100

1-3.1 (280 mg, 0.985 mmol) is treated with NMP (1 mL), DIEA (0.5 mL) and R52 (180 mg, 1.00 mmol) and the resulting mixture is stirred at 120 °C for 1 hour. The crude residue is purified by flash chromatography (SiO₂₎ 0-10% methanol/C^Ch) to afford the title compound (20 mg); m/z 406.4 [M+H].

Examples in table 1 listed with method 21 are synthesized in a similar fashion.

Method 22:

Synthesis of 5-(5-( l-|5-(2-aminopyridin-3-yl)-1.2,4-oxadiazol-3vllcyclobutvl}pvridin-2-vl)pyrimidin-2-amine (Example 105, Table 1)

Example 84 (50 mg, 0.12 mmol) is treated with THF (2.0 mL) and the mixture is cooled to -40 °C. Ammonia gas is bubbled through this solution for 5 minutes and the resulting mixture is heated in a sealed vessel at 100 °C for 24 hours. The solvent is removed in vacuo, the residue is treated with water (2.0 mL), and the resulting precipitate is collected by filtration and purified by flash chromatography (SiO₂, 0-10% methanol/CHiCh) to afford the title compound (20 mg); m/z 387.6 [M+H].

Examples listed in table 1 under method 22 are synthesized in a similar fashion from appropriate reagents.

Method 23:

Synthesis of 5-|5-(l-{5-|2-(methvlaniino)pyridin-3-vl]-l,2.4-oxadiazol-3vUcvcIobutvDpvridin-2-vUpvrimïdin-2-amine (Example 122, Table 1)

101

Example 84 (50 mg, 0.12 mmol) is treated with 2M methylamine in THF (2.0 mL, 0.4 mmol) and heated in a sealed vessel at 100 °C for 2 hours. The resulting mixture îs diluted with water (2.0 mL) and the resulting precipitate is collected by filtration and purified by préparative reverse-phase HPLC (50 mg); m/z 401.7 [M+H].

Examples in table l listed with method 22 are synthesîzed in a similar fashion.

Method 24:

Synthesis of 3-(3-( l-f6-(2-aminopvrimîdin-5-vl)pvridin-3-yl|cvclobutylÎ-l,2,4oxadiazol-5-yl)pYridin-2(lH)-one (Example 95, Table 1)

Ex. 84

Example 84 (50 mg, 0.12 mmol) is treated with 1,4-dioxane (2.0 mL) and lithium hydroxide (10% in water, 3 drops) and the mixture is heated at 70 °C for 24 hours. The resulting mixture is diluted with water (2.0 mL) and the precipitate is collected by filtration and purified by préparative reverse-phase HPLC (30 mg); m/z 388.5 [M+H]. Examples in table 1 listed with method 24 are synthesîzed in a similar fashion from appropriate reagents.

Method 25:

Synthesis of 5-(5-(l-I5-(pyrrolidin-l-vh-l_<2,4-oxadiazol-3-yl|cvclobutyHpvridin-2yllpvrimidin-2-amine (Example 76, Table 1) w/

102

Step 2

Step 1: synthesisof 5-{5-[l-(5-trichloromethyl-l,2,4-oxadiazol-3-yl)-cyclobutyl]pyridin-2-yl] -pyrimidin-2-ylamine (R55).

1- 3.1 (300 mg, 1.06 mmol) is treated with toluene (10.0 mL) and R54 (0.23 mL, 1.3 mmol) and the reaction is stirred at 110 °C for 2 hours. The resulting mixture is cooled to room température and partitioned between ethyl acetate and water. The phases are separated and the organic phase is washed with water and saturated aqueous NaHCO,·. The organic phase is dried over MgSO₄, filtered, and the solvent is removed in vacuo to afford R55 (354 mg); m/z 413 [M+H].

Step 2: synthesis of 5-(5- {i-[5-(pyrrolidin- 1-yl)-1,2,4-oxadiazol-3-yl]cyclobutyl)pyridîn-

2- yl)pyrimidin-2-amine (example 76).

R56 (0.07 mL, 0.9 mmol) is treated with DMF (5.0 mL) and R55 (354 mg, 0.860 mmol) and the resulting mixture is stirred for 30 minutes. The reaction is diluted with water and ethyl acetate and the phases are separated. The organic phase is washed twice more with water, dried over MgSO₄, filtered, and the solvent is removed in vacuo. The crude residue is purified by flash chromatography (SiO₂, 3% methanol/CH₂Cl₂) to afford the title compound (76.9 mg); m/z 364 [M+H].

Method 26:

Synthesis of 5-(5- ί 1 - 15-(dimethvlami ηοΐ-1,2.4-oxadiazol-3-vl 1 cvclob utvl 1 pyridin-2vDpyrimidin-2-amine (Example 15, Table 1) y

103

R57 (75.0 mg, 0.539 mmol) îs treated with HATU (284 mg, 0.746 mmol), TEA (0.30 mL, 2.16 mmol), and NMP (5.00 mL) and the mixture is stirred for 5 minutes. I-3.1 (153 mg, 0.539 mmol) is then added and the mixture is heated at 80 °C for 16 hours. The mixture is purified directly by préparative reverse-phase HPLC to afford the title compound (I6l mg); m/z 338.2 [M+H].

Method 27:

Synthesis of 2-[4-(3-n-[6-(2-amino-pvrimidin-5-vl)-pvridin-3-vl]-cvclobutylÎ-l,2,4oxadiazol-5-vl)-Pvrazol-l-vll-/VJV-dimethvl-acetamide (Example 59, Table 1)

R7

1-4.5 (200 mg, 0.516 mmol) is treated with DMF (2.0 mL), R7 (342 mg, 1.55 mmol), 2M Na₂CO3 (0.52 mL, 1.03 mmol), and bis(triphenylphosphine)palladium(n) dichloride (72 mg, 0.103 mmol) and the resulting mixture is heated at 80 °C overnight. The reaction is passed through a PTFE filter, the solvent is removed in vacuo, and the residue is partitioned between CH2CI2 and water. The phases are separated and the organic phase is washed with saturated aqueous NaHCO₃, dried over Na₂SO4, filtered, and the solvent is removed in vacuo. The crude residue is purified by reverse phase préparative HPLC to afford the title compound (40 mg); m/z 446 [M+H].

Examples in table 1 listed with method 27 are synthesized in a similar fashion from the appropriate intermediates 1-4. Examples 152, 153, 166, and 175 use tetrakistriphenylphosphinepalladium(O) as catalyst.

104

Method 28:

Synthesis of 5-(5-|l-(5-Pvridin-3-vl-1.2,4-oxadiazol-3-vB-cyclobutyl]-pyridin-2-vHpyrimidin-2-ylartiine (Example 73, Table 1)

1-4.1 (115 mg, 0.37 mmol) is treated with toluene/ethanol mixture (1:4 3.0 mL), R7 (61 mg, 0.44 mmol), 2M NazCO-, (0.40 mL, 0.81 mmol), 1,1 ’-bisdiphenylphosphinofeiTocene (20 mg, 0.04 mmol), and dichloro(i,l’-bisdiphenylphosphinoferrocene)palladium(II) (30 mg, 0.04 mmol) and the resulting mixture is heated at 90 °C for 3 hours. The resulting mixture is cooled to room température, filtered through celite and the crude residue is purified by préparative reverse-phase HPLC to afford the title compound (34 mg); m/z 372 [M+H].

Examples in table 1 listed with method 28 are synthesized in a similar fashion from the appropriate intermediate 1-4.

Method 29:

Synthesis of5-(5-H-(5-il-f2-(morpholin-4-ylÎethvl|-lH-pvrazol-4-vl]-1.2,4oxadiazol-3-vhcyclobutvl|pvridin-2-ylÎpyrimidin-2-amine (Example 140)

Example 90 (75.0 mg, 0.208 mmol) is treated with DMF (1.50 mL), Cs₂CO₃ (153 mg, 0.468 mmol), and R58 (77.5 mg, 0.416 mmol) and the resulting mixture is stirred at 60 °C for 1 hour. At this time R58 (25 mg, 0.134 mmol) and Cs₂CÛ3 (50 mg, 0.153 mmol) are added and the reaction is heated at 70 °C for 1 hour. The mixture îs purified directly by reverse-phase HPLC (10 to 70% acetonitrile/water/0.1% trifluoroacetic acid) to afford the title compound (18.0 mg); m/z 474.4 [M+H],

105

Examples in table l iisted with method 29 are synthesized in a similar fashion. Example 139 is heated at 70 °C for 1 hour and no second addition of reagents is needed. Example 141 is heated at 60 °C for 1 hour, then 1.5 équivalents of halide and 2.25 équivalents of base are added and heating was continued for an additional hour. Example 142 was heated at 70 °C for 1 hour, then room température over a weekend.

Method 30:

Synthesis of 2-|4-(3-H-[6-(2-aniinopvrimidin-5-vl)pviidin-3-vl|cvclohiitvl}-L2,4oxadiazol-5-vl)-lH-pyrazol-l-vll-N-tert-butvl-N-methvlacetamide (Example 143)

Step 1: Synthesis of [4-(3-{l-[6-(2-Amino-pyrimidin-5-yl)-pyridin-3-yl]-cyclobutyl}- l,2,4-oxadiazol-5-yl)-pyrazol-l-yl]-acetic acid ethyl ester (R60).

R60 is prepared according to the procedure for Example 65 step 1 using R59; m/z 447.4.

Step 2: Synthesis of [4-(3-( 1-(6-(2-Amino-pyrimidin-5-yl)-pyridin-3-yl]-cyclobutyl}-

1.2.4- oxadiazol-5-yl)-pyrazol-l-yl]-acetic acid (R61)

R61 is prepared according to the procedure for Example 65 step 2 using R60.

Step 3: Synthesis of 2-[4-(3-{l-[6-(2-Amino-pyrimidin-5-yl)-pyridin-3-yl]-cyclobutyl}-

1.2.4- oxadiazoi-5-yl)-pyrazol-l-yl]-/V-tert-butyl-A-methyl-acetamide (Example 143).

R61 (13.2 mg, 0.180 mmol) is added to a reaction vial. A stock solution of HATU (1.71 g) in dimethylacetamide (20 mL) is prepared and added (0.800 mL, 0.180 mmol) followed by a stock solution of R61 (502 mg) and DIEA (0.627 mL) in dimethylacetamide (DMA) (9.0 mL) (0.965 mL, 0.12 mmol R60 and 0.36 mmol DIEA).

The resulting mixture is shaken overnight at room température and the residue îs purified uA

106 by reverse-phase HPLC (acetonitrile/water/O.l% formic acid) to afford the title compound (23.1 mg); m/z 488.4 [M+H].

Examples in table l listed with method 30 are synthesîzed in a similar fashion.

Method 31

Synthesis of 5-il-f5-(l-Oxetan-3-yl-lH-pvrazol-4-vl)-H.2,4|oxadiazol-3-vl]cvclobutvlLI2.3^,lbipyridinvl-6'-vlamine (Example 145)

R64 1-1.1 R65

R63

Step 2

NH₂OH

H

R11

R67

Step 4

R38

R66

Example 145

Step 1: Synthesis of l-[6-(5-amino-pyrazin-2-yl)-pyridin-3-yl]-cyclobutanecarbonitrile (R65) ln a 20 ml microwave reaction vessel are combined R63 (250 mg, 1.44 mmol) and R64 (520 mg, 1.59 mmol) in toluene (8 ml). The mixture is degassed using argon after which

107 tetrakis(triphenylphosphine) palladium (0) (100 mg, 0.09 mmol) is added. The réaction is degassed once more, capped and warmed to 115^l'C for lh. Upon cooling to ambient température, I-l.l is introduced along with tetrakis(triphenylphosphîne) palladium (0) ( 120 mg, 0.10 mmol). The vessel îs capped and warmed to 115°C overnight. After this time the reaction is cooled and concentrated. The crude is suspended in DCM/MeOH, treated with silica gel and concentrated. The resulting solid is purifîed via flash chromatography (Silica gel, 0-10% MeOH/DCM) to give R65 (220 mg); m/z 252.2 [M+H],

Step 2: Synthesis of l-[6-(5-amino-pyrazin-2-yl)-pyridin-3-yl]-N-hydroxycyclobutanecarboxamidine (R66)

To a stirred suspension of R65 (220 mg, 0.88 mmol) in éthanol (4 ml) is added hydroxylamine (50% aq. solution, 1 ml). The resulting mixture is stirred at 80°C overnight and cooled to room température. The reaction is concentrated and the remaining residue is diluted with water. The precipitated yellow solid is collected via filtration and washed with water to give R66 (115 mg).

Step 3: Synthesis of 5-(5-( 1-(5-( lH-pyrazol-4-yl)-[ 1,2,4]oxadiazol-3-yl]-cyclobutyl}pyridin-2-yl)-pyrazin-2-ylamine (R67)

To a suspension of RI 1 (68 mg, 0.61 mmol) in THF (5 ml) is added CD! (98 mg, 0.61 mmol) at room température. The mixture is stirred at 50°C for 30 minutes after which time R66 (115 mg, 0.40 mmol) is added. The resulting mixture îs heated at 80°C for 3 hours, cooled to room température and treated with acetic acid (AcOH) (8 ml). The reaction is warmed to 80°C and stirred overnight. Upon cooling to room température, the reaction îs concentrated and diluted with water. The product is extracted into DCM (2x). The combined organics are washed with brine, dried (MgSO4), filtered and concentrated. The remaining residue is purifîed via flash chromatography (Silica gel, 0-10% MeOH/DCM) to afford R67 (50 mg); m/z 361.2 [M+H],

Step 4: Synthesis of 5-{l-[5-(l-Oxetan-3-yi-lH-pyrazol-4-yl)-[l,2,4]oxadiazol-3-yljcyclobutyl}-[2,3']bipyridinyl-6’-ylamine (Example 145)

A mixture of R67 (50 mg, 0.14 mmol), R38 (51 mg, 0.28 mmol) and potassium carbonate (38 mg, 0.28 mmol) in DMF (2 ml) are stirred at 80°C over night. After this time the reaction is cooled to room température and poured into water and EtOAc. The layers are

108 separated and the aqueous phase is extracted twice more with EtOAc. The combined organics are dried (MgSO4), filtered and concentrated. The remaining residue is purified via flash chromatography (Silica gel, 0-8%MeOH/DCM) to afford the title compound (35 mg); m/z 417.3 [M+H].

Examples in table l listed with method 31 are synthesized in a similar fashion.

Method 32

Synthesîs of 1(3 ] l-|6-(2-Ainino-pvrimidin-5-yl)-Dvridin-3-vl|-cvclobutvll-|1.2.4|o xadiazol-5-vB-piperidîn-4-ol (Example 154)

1-2.1

Step 1

COI

CH3CN

Step 2

POCI3 pyridine

Example 154

THF

Step 4

Pd(PPh₃)_asat'd Na₂CO₃

R7

Step 1: Synthesîs of3-[l-(6-chloro-pyridin-3-yl)-cyclobutyl]-[ 1,2,4]oxadiazol-5-ol (R68)

To a solution of 1-2.1 (2 g, 8.862 mmol) in CH₃CN (50 mL) is added CDI (3.593 g, 22.16 mmol) in a pressure flask. The reaction mixture is stirred at 75°C for 18 hours. After this time, the reaction mixture is concentrated in vacuo and the resulting residue is quenched

IN HCl aqueous solution and extracted with ethyl acetate twice. The organics are combined and washed with brine, dried over Na₂SO₄, filtered and concentrated in vacuo to afford the title compound (2,13 g) as an off white solid; m/z 252.4 [M+1].

109

Step 2: Synthesis of 2-Chloro-5-[l-(5-chloro-[l,2,4]oxadiazol-3-yl)-cyclobutyl]-pyridine (R69)

To a solution of R68 (300 mg, L192 mmol) in DCM (4 mL) îs added POCI₃ (0.175 mL,

I. 910 mmol) and pyridine (0.481 mL, 5.960 mmol) in a pressure flask. The reaction mixture is heated in a microwave at 120°C for 1 hour. After this time, the reaction mixture is poured into ice water and extracted with DCM twice. The organics are combined and washed with brine, dried over Na₂SO₄, filtered and concentrated in vacuo, The crude is purified by flash chromatography (SiO₂, 5-40% EtOAc/heptanes) to afford the title compound (98 mg) as a light yellow oil; m/z 270.2 [M],

Step 3: Synthesis of l-{3-[l-(6-chloro-pyridin-3-yl)-cyclobutyl]-[l,2,4]oxadiazol·5-yl}piperidin-4-ol (R71 )

To a solution of R68 (98 mg, 0.363 mmol) in DMSO (1.5 mL) is added R70 (44.1 mg, 0.436 mmol) and DIEA (0.158 mL, 0.908 mmol). The reaction mixture is stirred at room température for 1 hour. After this time, the reaction mixture is quenched with water and extracted with EtOAc twice. The organics are combined and washed with brine, dried over Na₂SO₄, filtered and concentrated in vacuo to afford the title compound (121 mg) as a light yellow oil; m/z 335.1 [M+1].

Step 4: Synthesis of l-(3-{ l-[6-(2-amino-pyrimidin-5-yl)-pyridin-3-yl]-cyclobutyl}- [l,2,4]oxadiazol-5-yl)-piperidin-4-ol (Example 154)

To a mixture of R7 (96.4 mg, 0.436 mmol) and Pd(PPh₃)₄ (42 mg, 0.036 mmol) in a microwave vial is added the DMF (4 mL) solution of R71 (121 mg, 0.363 mmol) and 2M Na₂CO₃ aqueous solution (0.726 mL). The reaction mixture is purged with argon and then heated in a microwave at 110°C for 45 minutes. After this time, the reaction mixture is quenched with water and extracted with EtOAc twice. The organics are combined and washed with brine, dried over Na₂SO₄, filtered and concentrated in vacuo. The crude îs purified by flash chromatography (SiO₂, 1.2-10% MeOH/DCM) to afford the title compound (22 mg) as a white solid; m/z 394.2 [M+1].

Method 33

Synthesis of 3-14-(3-il-16-(2-amino-pvrimidin-5-vh-Pvridin-3-vl|-cyclobutyl}-

II, 2,4loxadiazol-5-y0-pyrazol-l-vll-2,2-dimethvl-propionaniide (Example 147)

110

Step 3

Step l: Synthesis of3-[4-(3-{l-[6-(2-amino-pyrimidin-5-yl)-pyridin-3-yl]-cyclobutyl}- [1.2.4] oxadiazol-5-yl)-pyrazol-l-yl]-2,2-dimethyl-propionic acid ethyl ester (R73)

To a solution of Example 90 (300 mg, 0.832 mmol) in NMP (10.0 mL) is added R72 (343 mg, 2.08 mmol) and CS2CO3 (325 mg, 0.999 mmol) and the resulting mixture is stirred at l00°C for 4 hours. At this time another charge of R72 (27 mg, O.l64 mmol) is added and the reaction is heated at 100 °C ovemight. The resulting mixture is cooled and diluted with ethyl acetate and water. The phases are then separated and the organic phase is washed with water and brine, collected, dried over \a2SO4. filtered, and concentrated in vacuo. The residue is purified by flash chromatography eluting 0-10% methanol/DCM to give the title compound (170 mg); m/z 489.4 [M+H],

Step 2: Synthesis of 3-[4-(3-{ l-[6-(2-amino-pyrimidin-5-yl)-pyridin-3-yl]-cyclobutyl}- [1.2.4] oxadiazol-5-yl)-pyrazol-1 -yl]-2,2-dimethyl-propîonic acid (R74)

R73 (170 mg, 0.348 mmol) is treated with THF (1.60 mL), water (0.80 mL), methanol (0.40 mL), and lithium hydroxide monohydrate (43.9 mg, 1.04 mmol) and the resulting mixture is stirred at 45 °C for 1 hour. The reaction is quenched with IN HCl (1.04 mL, 1.04 mmol) and the mixture is concentrated in vacuo to give the title compound (160 mg).

Step 3: Synthesis of 3-14-(3-(1 - [6-(2-amino-pvrimidin-5-yl)-pyridin-3 -yll-cyc lobutyl} [ 1,2.41oxadiazol-5-vl)-pyrazol-1 -vl1-2,2-dimethyl-propionamide (Example 147)

111 _R74 (160 mg, 0.348 mmol) is treated with HATU (186 mg, 0.488 mmol) and DMF (3.5 mL). Ammonia gas is then bubbled through this mixture for 2 minutes twice with 5 minutes in between and the vessel is capped and stirred for l hour. The resulting mixture is then purified dîrectly by reverse-phase préparative HPLC (20-80% acetonitrile/water/0.1% trifluoroacetic acid (TFA)) to give the title compound (122 mg). Examples in table l listed with method 33 are synthesized in a similar fashion.

Method 34

Synthesis of 3-14-(3-]l-[6-(2-amino-pvrimidin-5-vD-pvridin-3-vll-cyclobutvn10 11.2.4|oxadiazol-5-vlÎ-pyrazol-l-vll-2,2-dimethyl-propionitrile (Example 148)

TFAA (73 pL, 0.522 mmol) is treated with CH₂C1₂ (1.0 mL) and pyridine (42.2 pL, 0.522 mmol) and cooled to 0 °C. To this mixture îs added a solution of Example 147 (48.0 mg, 0.104 mmol) în CH2CI2 (0.5 mL) and the resulting mixture is warmed to room température and stirred for 1 hour. The reaction is then quenched by the addition of saturated NaHCO; and stirred for 30 minutes. The mixture is diluted with CH₂C12and water and the layers separated. The aqueous layer is extracted again with CtLCTand the combined organics are dried over Na₂SO₄, filtered, and concentrated. The crude residue is then treated with THF (1.0 mL), water (0.5 mL), methanol (0.2 mL), and lithium hydroxide monohydrate (8.6 mg, 0.21 mmol) and the resulting mixture is heated at 40 °C for 30 minutes. The mixture is then diluted with saturated NaHCOj and ethyl acetate and the layers separated. The aqueous is then extracted with ethyl acetate again and the combined organics are dried over Na₂SÛ4, filtered, and concentrated. The resulting residue is triturated with acetonitrile to give the title compound (12.0 mg).

Examples in table 1 listed with method 34 are synthesized in a similar fashion.

112

Method 35

Synthesis of 5-|5-(l-(5-l l-(2-amino-2-methvl-propvl)-lH-pyrazol-4-vl)H,2,4|oxadiazol-3-vl}-cyclobutyl)-pvridin-2-vl|-pvrimidin-2-vlainine (Example 150)

Step 1: Synthesis of {2-[4-(3-{l-[6-(2-amino-pyrimidin-5-yl)-pyridin-3-yI]-cycIobutyl}- [l,2,4]oxadiazol-5-yl)-pyrazol-l-yl]-l,l-dimethyl-ethyl}-carbamic acid tert-butyl ester (R75)

R74 (110 mg, 0.202 mmol) is treated with toluene (1.00 mL), D1EA (70.3 pL, 0.403 mmol), Fbutanol (1.00 mL), and diphenylphosphoryl azide (69.4 mg, 0.252 mmol) and the resulting mixture is stirred at 85 °C overnight. An additional charge of t-butanol (0.5 mL) is then added and the heating is contînued again overnight. The resulting mixture is diluted with ethyl acetate and washed with water and then saturated NaHCOj. The organics are dried over Na₂SO₄, filtered, and concentrated and the resulting residue is purified by flash chromatography eluting 0-10% methanol/CH₂Cl₂ to give the title compound (33.0 mg).

Step 2 Synthesis of 5-(5-( 1 - {5-Γ1 -(2-amino-2-methyl-propyl)-1 H-pyrazol-4-yl][ 1,2,41oxadiazoÎ-3-vH -cycÎobutyl)-pvridin-2-yll-pyrimidin-2-ylamine (Example 150) jlA

113

R75 (33.0 mg, 0.062 mmol) is treated with CH₂Cl₂ (i.O mL) and TFA (0.25 mL) and the resulting mixture is stirred for l .5 hours. The mixture is then concentrated to dryness and purified directly by reverse-phase préparative HPLC to give the title compound (21.0 mg).

Table 1. Final compounds.

Exa mpl e	Structure	Method	Rétention time	m/z	LCMS method
1	O __ _N .—s oA— nYJ θ A J H₂N N	10	6.56	556.8	E
2	/Xr H ï A ⁰ Ά h₂n A ⁰	2	4.10	444.7	E
3	Aj _X /“L \h M^YY ^N'O A J h₂n n	19	3.79	456.7	E
4	N Y N ^u A J h₂n n	10	4.35	361.6	E
5	rYvQ ΑγΧ ^{n 0} \ h₂nY	10	2.33	385.1	I

114

6	νΧ-^Ν ⁰ Λ 2 η₂ν ν	10	2.27	385.0	I
Ί	rlvOr JL f Ν-η ⁰ Ν-γ-^'Ν ⁰ η₂νΊ^χ	10	1.58	448.9	1
8	^ΓΓΙ>-4Α^ν> n Ar ν ^ϋ / Λ J η₂ν ν	2	4.51	415.6	Ε
9	αΛ-^ν λΑα ΤΤΙΤ V Ν'^Τ'Ν ⁰ [> A J η₂ν ν	2	6.11	427.6	Β
10	\Ζ ΝΗ„ AVW J -οΝ-^νη Ν Α^ Ν ^U Λ J η₂ν ν	18	3.97	376.6	Ε
11	Γ^νΟ nAV ^Ν'° Τ^ο Αχ °'^ η₂ν ν	10	2.14	449.2	C

115

12	/=Ν _Η λΑ ^{ν ηο} \ η₂ν ν	2	5.95	459.6	Β
13	ατΛηΗ ΑΑν ⁰ Η₂Γ+ ⁰	2	6.70	473.6	Β
14	ΑΑν-Υ JI ν-οΎγ-ν Ν Ν ^υ A X η₂ν ν	ΙΟ	4.23	362.6	Ε
15	_ζυΧ-ν ^ζf Ύ Η Α\ νΑΎ ^N'û ^ΧA J η₂ν ν	26	1.87	338.2	C
16	Λ^ν\Α ΐΥΥ Ηθ/ η,νΎ ⁰	5	4.36	445.7	Ε
17	γΑΧαΧυ Ν ΥΧ «-Ο ·^ ° A 7 η₂ν ν	ΙΟ	1.97	450.2	C

ll6

18	-+X.AA....N Η ΑΑ ^ηοΑ η₂ν ν	2	5.93	457.6	Β
19	NFL ζ\ Ο'ς'-Α /\ ?Ό Α^ΑΑΓ^νχ_-/~7 ν'^Α^Α ^ν~° Η-,Ν^Α	10	2.01	450.2	C
20	^ν-α Η₂Ν^Α F ^F	10	7.04	443.6	Β
21	-γΟΑ^-Ν /=\ Η Γ Τ “ +Α νΆ*ν“ ^ν'° Τι Τ ^Η°~⁷	2	6.19	459.6	Β
22	nArVO-o _νΑΑ n-cTW > η₂ν^Λ'Α ^οη	2	6.17	432.6	Β
23	AÛAA A ν Α' Ν' ^νό Ν A A η₂ν Ν	10	3.33	378	G

117

24	Aya A ⁿ° ^N Λ J h₂n n	10	3.23	362	G
25	zA\.+ ΛΝ ijjf Ha nAV ⁿ'° il Λ J ⁿa H₂N N	10	3.23	412	G
26	^AAn χ Q ^-¾. _JL J N~o \=/ N Ύ N ^u Λ J h₂n n	10	3.22	402	G
27	N Ύ N ° Λ J h₂n N	10	2.76	411	G
28	/ΐΑγ AA [i T μ άαν ’lA'¹'^ °	10	3.42	418	G
29	O a^oh Αλζ¹* AJ 1<A^NnAn ^u Λ J H_ZN N	27	3.19	419	G
30	A A^{H 1} γΑγΝ AA f J ï Aan nA^n^ ⁿ'° Λ J H₂N N	27	3.37	433	G

118

31	AvM ^Ν-0 η₂ν'^'ν'	7	4.02	438.6	E
32	jA^y-xy™ /¾. At fi N-o n Ar n ^υ A X h₂n n	1	2.05	387.2	C
33	Λαα ^N’° Λ J ^H h₂n n	2	3.93	461.7	E
34	^aCn /=n. /> ΓΤ AA /Aⁿ A νΑΑγ ^N'° A J ° N H₂N N /	2	4.82	512.8	E
35	^xSA-n /=n, /> _ Π Ϊ'ΑΑν n A'_N ⁰ jf η,νΑ ⁰ °^H	6	4.88	485.7	E
36	,γ\Α> /=\ /A ΠΪΚ/ν N^A 'N ⁰ A y ⁰ O H₂N N /	6	5.70	499.8	E
37	Sa* _,n nyV ^Ν'θ ⁿ'ⁿη,ν^Α	13	4.24	376.6	E

119

38	Ον ^N-°Ay’ ιι J ^x η₂ν^Λν _z°	4	3.98	514.8	E
39	Ajx ⁿ>^AⁿQ^nh Aj n ⁰ A°\ h₂n^AA ⁰	4	3.97	514.8	E
40	fTyvCXM rX^'N ° y-o A J <T h₂n n	4	3.99	514.8	E
41	îyiAV-A /Α^νΟ^νη Or ^N c°^H h₂nO ⁰	5	3.87	500.7	E
42	f j^{N 0} >-OH h₂nO ⁰	5	3.89	500.7	E
43	iAfyo-<A_Hn + n ^u A ') h₂n n	2	1.86	457.2	C
44	aAL-N /=\ H AÎAA XA ^{n ho} \ h₂n n	2	4.23	445.7	E

120

45	N N ^υ χ A J ^0H h₂n n	2	1.33	471.2	F
46	AHoMl·) 'ί, ΐ” HO A A h₂n n	2	4.23	445.7	B
47	Λ J ^A h₂n n	2	1.12	556.2	F
48	.Ao<x. nVn ⁰ A J h₂n n	2	1.26	457.2	F
49	Ά — N Γ~'·° _N-Vn^{zJ N}'° A 9 h₂n n	2	2.05	505.2	C
50	_naA? ⁿ'° A J h₂n n	2	2.22	534.2	C
51	pAyAp n-AX ⁿ-°AP	2	1.84	493.2	C

I2l

52	⁰ 0 A J h₂n n	2	1.97	519.2	C
53	A\ OH ,/ÀA r=\ r~\ _/~3 r Y Y *_/ ,y-_N n·^ o ν-Av HahAbT	3	1.10	528.2	F
54	Aγγ N/* N hA'+r'MM ^N° ^0H h₂iA^z	11	1.27	433.4	A
55	γχΛΑ /^N JÛr ^N A, h₂n n	12	1.27	417.4	A
56	nAy-OV A fi N-_O ^Z ^-N N A N ^υ 0 A fi h₂n n	27	3.41	445	G
57	vA/A nAn^{zJ n}'° ⁿ A / H₂N N	1	3.51	415	G
58	.zAAⁿ /^n hn ΑΤΧ^α N A IM ^υ A fi h₂n n	27	3.07	432.2	G

I22

59	,Ν /-Ν 0 [ι Τ ΧΆΑ A ^Ν'Ο A J η₂ν ν	27	3.15	446	G
60	γγΧΑ-Ν ^νη [ Τ ϊ f-X υΑ Αγν ^Ν~° ^Ν A fi η₂ν ν	20	0.60	457.3	F
61	rAvzyO' Λ A f Ν-ο ^Ν Ν +/ Ν ^υ Λ fi η₂ν ν	8	2.75	470.2	G
62	//ΥγΖΥθ^ΗnXV ^Ν-° A fi η₂ν ν	19	1.75	455.4	C
63	Αν Ν Ν ⁰ A fi η₂ν ν	II	1.37	389.4	A
64	ΆΥΥγΆ A fi ' η₂ν ν	11	1.47	403.4	A
65	ζ\Α-ν /-ν _ΧΥΙ/Υρ Ν Ν ^υ ί η,ν^ΛΧ °^Λ°^η	16	1.31	447.4	A

123

66	AYrV-C' J N-o' Vn F N YY N ^υ j A J F h₂n N	15	1.43	411.4	A
67	ΑΠΑχ N Y N ^υ F A J H₂N N	11	1.33	407.4	A
68	xA\AAn Λ-n F ΑΠΑυ N Y N ^{υ F} A J h₂n n	11	1.38	425.5	A
69	xî^;îx''AA-'-N Λ-ν f ΑΠΥΧ N V N ^U F A J h₂n N	11	1.48	443.4	A
70	i 7 A rvk A N~o > nY n ^υ 1 A J cAnh₂ H₂N N ²	il	3.97	418.3	E
71	yAA A' ί Ύ A xvk A A N-o Ί N Y N ^υ ' A J ^οχΑ H₂N N 0	14	1.72	453.4	C
72	.0 Ayo N Y N ^υ A J h₂n n	27	3.10	402	G

124

73	Γ^ττ^ΝναΧ ^ν'°^ Αα Λ J η₃ν ν	28	1.69	372	H
74	χΥ_ν-Ν /=Ν ^xy νΑν ^Ν ο A J η₂ν ν	10	6.45	386.5	B
75	AaSt^v-Yj χ'ΐχ. A Ν-ίΐ^ A Ν Ν ^υ A J η₂ν ν	10	2.94	361	G
76	jTjyVnQ n'AYV ^ν'Ο^Ζη₂ν^Λν^	25	3.53	364	G
77	A J Ν-_Ο ^Ζ \-Ν ν AA ν A ^λ A J ⁰ η₂ν ν	10	2.96	402	G
78	ΧΧΑΑν _/A ίι Τ ί. ΥΎΰ N AA N ^υ / YN^'iA	!O	3.26	375	G
79	/Υν^Νκ AVU Π Ί A Ai A nAA ^N'°	10	3.59	410	G

125

80	A> ^h αΑύ' ⁿa—/A /V J N- Q '7\ N ^Y N ^u A J h₂n n	10	3.34	375	G
8!	^AvCA’ zx A J N-O ^=^{7 0} N N ^υ A J H₂N N	l	1.25	430.2	F
82	V κι Λ-N OH î9A;AA N» N ^U A J h₂n n	17	1.33	430.2	F
83	Πμ^γΝ>Α/^^ν N N ^u h₂n\^z	l	1.58	397.6	F
84	nAA-A AJ h₂n n	21	5.57	406.4	D
85	zî;^ /v? N-~r> N 'Y N ^u / h₂n^A	21	2.34	386.2	F
86	_Λ A m A=N /Y-vy / \ f j Y HJ nY> ⁿ-° _> H_;W N'	10	2.02	402.2	C

126

87	N-yV ^Ν'°	21	5.14	372.4	D
88	>Α^ν.Τ> Jl Τ Ύ SJ N^sy^sN-^{J N}-° S A J ^a h₂n n	1	6.66	406.5	B
89	A ^X0 _NAv ^N'° A A h₂n n	10	1.23	457.2	F
90	yyAA ^Ny—A n ^H-À J n-o^AA N Y n ^u A A h₂n n	10	4.84	361.6	D
91	AvO jAj ^N ^{N 0} OH η₂νΆ	10	1.74	388.2	E
92	Aîvo A? ⁿ~° ⁿΗ₂Ν^Ά	10	1.86	373.2	C

127

93	rpiV-Q nV'n'^{J N}'O 'o H,_NV	10	2.53	402.2	C
94	fr^v-^A n^Z5/n^{J N}'O ^S '	l	6.78	406.5	B
95	O °x\ ^H nY- n ⁰ A J h₂n n	24	5.57	388.5	B
96	nXn^{J n}'° >ⁿ A J °s h₂n n	10	2.72	432.2	C
97	nV'n'-J A J ^H0 h₂n n	10	1.75	402.2	C
98	yAaⁿ _x /T^N _ΝγΑτ °^J η,ν^'Α	10	1.92	362.2	C

128

99	Αγ/γ_α ⁿ'° h₂n^A	l	1.58	406.2	A
ιοο	nA ⁿ'° A 5 h₂n n	10	4.88	373.5	D
ΙΟΙ	nA^A ⁿ”° ' \	10	2.13	386.2	C
102	Α/ΥγΑ< ^A 7 N-AAn N N ^υ A J h₂n n	10	1.92	375.2	C
103	ΑΑνΑ -A JJ Ν-οΎ^Ν N A N ^υ / h/i^nT	10	2.08	389.2	F
104	mv-O nAV ⁿ'° ^VnA J h₂n n	10	1.80	373.2	C

129

105	/\ ^Η2^Ν n V'_N ⁰	22	5.97	387.6	Β
106	1 \|Γ η ^χ)—<^ζ 7 νΑΎ ^Ν'° V A 7 ^Η*^Ν η₂ν ν	22	4.43	387.6	D
107	_Λ \Ζ Μ <-Ν Ζγ ΥΤί 7 η,Ζ/	24	4.34	388.6	D
108	ΓΑΓΑΓζ χγζ ^ν~° ν Λ 7 η₂ν ν	24	5.75	388.5	Β
109	ΓΥΓαΥ-Α η A J Ν-ο VN Ν ν ^υ J A J ^fTf Η₂Ν ν ^{f f}	10	5.75	440.5	D
I ΙΟ	y\zLn Λ^Ν\ ^ζ ν^Τ'ν ⁰ A J η₂ν ν	2	5.50	415.7	D

130

11)	nX' N ⁰ A fi η₂ν ν	2	5.59	387.5	Β
H2	⁰ η₂ΖΖ	2	6.35	441.6	Β
Ü3	A\J\/N /=\ Η νυν ⁰ Λ fi η₂ν ν	2	4.55	401.6	D
H4	αΑζζ Ν Ν ^υ ' A fi η₂ν ν	2	6.36	429.6	Β
ll5	Ν^’- Ν ⁰ _ΗηΑ aJ η₂ν ν	2	4.47	43 1.7	D
H6	A-ALn /=\ ^ζ ΠΓΎ η/ν^ΗZZV ^Ν'Ο A fi η₂ν ν	2	2.04	445.2	C
ll7	Ζττ Ζ_Ζ^ Α- ν ο nXv ^A^;jr A fi η₂ν ν	2	2.51	459.2	C

131

ns	/=N h N^:'>'V ⁰ Λ J h₂n n	2	2.14	445.2	C
ll9	XjXvcA⁰ A 9 h₂n n	9	2.04	450.2	C
120	.y-Ay /a C ji n <>^NHnVv ⁿ° ⁿ Λ F h₂n n	1	3.99	362.6	E
121	AⁿA _N-yM ⁿ~° r^NA J ^z H₂N N	21	6.78	389.5	E
122	Aa A 9 h₂n n	23	5.32	401.7	D
123	X- J n-c? ^xN '^ N ^υ A J h₂n n	10	4.86	378.5	E

132

124	Λ -) η₂ν ν	10	4.53	375.6	Ε
125	___ S< Ν /=^Ν γΧ Ν ''' _Ν ⁰ A J η₂ν ν	2	4.78	470.7	D
126	n-(?)=n η₂ν^ΑΑ ^χ	23	6.60	415.6	Β
127	»χΑα. Λ X η₂ν ν	10	4.64	375.6	Ε
128	Γ ϊ Τ >—< / νΆ'Χ ^ν~ο >^ν«zJ π	23	5.14	457.7	Ε
129	nAORaQ	10	3.40	373	G
130	γΛχΑ λ A J Ν-η ^Ν nVn ^ν Ο A J η₂ν ν	10	3.47	387	G

I33

I3l	ΑγΥ/Υ _NXJ -o ⁿ' A J h₂n n	10	3.10	375	G
132	γΑγΝΧΝ XJ XH A y H₂N N	1	1.56	361.2	I
133	\ / ^HγΑγΝ. ,^N'N r T y i ,<_X/A.N N'O N X< ^u h_znV	10	1.77	375.2	I
134	f Y Y _nyXvN No A ) h₂n n	10	1.71	375.2	I
135	ζ^ΥΑν Xnh r iï Y Y—C ¹II f \yN n-o Xⁿn / η₂ν'^Ύ	10	1.68	375.2	I
I36	o ^n?><Ln i _NAn_oA Η,_ΝΧ	28	3.47	419.2	G

134

137	,0 χΝΥχΑν Α\ μ X « A ^-ν Ν \|Γ A JI Η₂Ν Ν	28	3.12	402.2	G
138	Ο yJACy αχ, _naûax° Ν \|f ο aJ η₂ν ν	28	3.11	402.1	G
139	jfyX’V'CA ο ϊ'γΧ ⁰ Χλο Η₂Ι\Γ Ν	29	1.06	479.2	F
140	/=?ν ΑΪΧΑ Ν V Ν ^υ / Αο	29	0.94	474.4	F
141	/αΑΑν υν ΑΪΙ_ΟΑ A J n η₂ν ν ν	29	1.08	400.4	F
142	ΑΖυΑΗ ί Ύ » ΧΑν_χ Λ J Χχ η₂ν Ν 1	29	0.88	432.4	F

135

143	A A F* N A l 0^ΛΧ H₂N N	30	0.91	474.3	J
144	_zaA ,N /*n ΑΠ-χΑ N^YN ⁰ ] hX'A °	30	0.95	488.4	J
145	/vAa aⁿ \|vQaxS?₀ h₂n A	31	0.65	417.3	J
146	_r/-'_?.X^A_k /%n H₂fAY /OH	31	1.05	433.4	F
147	χαΆΆ-Ν /=n j II T hVN Q Av ^N-° χΑ η,ν'Α	33	1.08	460.4	F
148	Al J 1 AA a AA X h₂n n	34	1.2	442.4	F

136

149	/=N zdïlTW nVn ^{n 0} Τ' HjN'^'n' ^{0 NH}2	33	l .06	446.4	F
150	A\A,'N /n £ j s a%A nAV ^N'° A H_zN^k ^H^N	35	0.95	432.4	F
I5l	ζ'^<ΧγΑ,Ν /=^N y_:,x y i-o^-v </ N N ^υ \| _w kA£ iii h₂n N n	34	0.76	428.3	J
152	a^a£n an Îl Ί ^N Vo H/l lX	27	0.58	416.3	J
153	XjjVCX < Y N ^U h₂n^n^	27	0.59	432.3	J
154	Μί£ΧΑ” N X N ° A J h₂n n	32	0.59	394.2	J

137

155	γΑΑ^Ν Ν ^νΑγ^{>ν ν ο} X ηΖΧ '7 ⁰	30	0.73	458.3	J
156	αΑΟ^ν αν <Α A ην Ad Η,Ν Ν 1 Ο⁷	30	0.75	502.3	J
157	,_;ΑΑ Α’^ν _νΑΠΑ\ u ιΑιΑ ΗνΆ η₂ν ν	30	0.78	460.3	J
158	ΑχΑα Α--Ν ,ΑΥνΆ Ν Ν ^υ u ,Α A ην Ad η₂ν ν Jj	30	0.73	466.3	J
159	ααα A J 'Λ Η,Ν Ν 1 A	30	0.79	516.4	J

138

160	Λ J η₂ν ν	A Ν	χΑ-Ν Η N-q	Αν	30	0.8	472.3	J
Λ	A
161	Α X η₂ν ν	A ' Ν	\Αν Η ^χ) Ν-ο	/=Ν A	ς	30	0.75	502.3	J
				—ο
162	Ar A J η₂ν ν	XX Ν	ΧΑ-ν Η ^χ) Ν-ο	/^Ν Αχ Ά		30	0.77	460.3	J
163	A η₂ν ν	Ο Ν	Ίί γ- N-Q	/=Ν 0 VnAÎ	Ν'' 1	27	0.52	445.2	J
164	,Ν. X J η₂ν ν	XX Ν	>Αν τ > Ν~ο	/=Ν X ο	Ν I	31	0.56	446.3	J
165	ΝΑ A J UN Ν 1	Λ J Ν	>Αν Τ V Ν-ο	/=Ν χ_;	ΟΗ	11	0.93	447.3	J

I39

166	Α''''_ν·Α.A ÆN . ί ϊ Ν Χζγγ ^Ν0 ^ ΟΗ	27	1.58	457.2	1
167	ΥαΑΑν λν ΑτΑΑΑ ^χνά₀ η-,ν^Ό	27	1.53	441.2	I
168	\ if a y-V^N^ ΑγΜ Ν-ο H	ΙΟ	0.66	389.3	J
169	AaAaj /^n _M L ï I AA îW ^N'° Vo	ΙΟ	0.61	431	J
170	aACn /SN n LJ! H+a _ryV ^N'° h.n ή	II	0.64	401.3	J
I7l	γΑ*Α-Ν /= N jfAA Ν-0^^Νχ^θ Η-,Ν^Ν	11	0.67	419.3	J

140

172	/γΧΑ-Ν An H,N / OH	11	0.62	447.4	J
173	» 1 J ! YM' f'pr ⁿ-° HN A 1	11	0.66	415.5	J
174	a\JY. ,. n Y’N aAXAcYA γ/	10	0.9	375.2	J
175	_zAY-N /=5N _x if J IcA YoH nYYn ^{0 0H} A J h₂n n	27	0.61	447.4	J
176	zA-A/N^ an χΑΤγΑγθ HN^Y 1	12	0.65	431.3	J
177	Αχ,Χ.^Ν, A_N χγ HN^Y / OH 1	II	0.66	447.2	J

Analytîcal Methods LC-MS Method A ,

I4l

Column	Agîlent Zorbax Cl8 SB 3.5pm, 4.6x30mm Ambient température
Mobile phase	A = Formic acid (aq) 0.1 % B = Formic acid (acetonitrile) 0.1%
Flow rate	2.5 ml/min
Injection volume	7 μΐ
Detector	200-600 nm (nominal)
Gradient	Time (mins)	%B
	0	5
	1.7	95
	2	95
	2.1	5
	2.3	5

LC-MS Method B

Column	Agilent Zorbax Eclipse XDB- C8 5pm, 4.6x150mm Ambient température
Mobile phase	A = Formic acid (aq) 0.1% B = Formic acid (acetonitrile) 0.1%
Flow rate	1.5 ml/min
Injection volume	7μ1
Detector	200-600 nm (nominal)
Gradient	Time (mins)	%B
	0	1

142

2	20
7	95
9	95
9.3	l
10	I

LC-MS Method C

Column	Agilent SB-C18 l.8pm, 3x50mm Ambient température
Mobile phase	A = Formic acid (aq) 0.1% B = Formic acid (acetonitrile) 0.1%
Flow rate	1.5 ml/min
Injection volume	3μ1
Detector	220 and 254 nm (nominal)
Gradient	Time (mins)	%B
	0	5
3.8	90
4.5	100

LC-MS Method D

Column	Agilent Zorbax Eclipse XDB- C8 5μιη, 4.6x150mm Ambient température
Mobile phase	A = Formic acid (aq) 0.1% B = Formic acid (acetonitrile) 0.1%

143

Flow rate	l .5 ml/min
Injection volume	7μ1
Detector	200-600 nm (nominal)
Gradient	Time (mins)	%B
	0	l
2	l
7	5
9	95
9.3	95
10	5

LC-MS Method E

Column	Agilent Zorbax Eclipse XDB- C8 5 pm, 4.6x150mm Ambient température
Mobile phase	A = Formic acid (aq) 0.1% B = Formic acid (acetonitrile) 0.1%
Flow rate	1.5 ml/min
Injection volume	7μ1
Detector	200-600 nm (nominal)
Gradient	Time (mins)	%B
	0	5
7	95
9	95
9.3	5
10	5

LC-MS Method F yy'

144

Column	Agilent SB-C18 1.8 pm, 3x50mm column Ambient température
Mobile phase	A = Formic acid (aq) 0.1% B = Formic acid (acetonitrile) 0.1%
Flow rate	1.5 ml/min
Injection volume	3μ1
Detector	220 and 254 nm (nominal)
Gradient	Time (mins)	%B
	0	12
	0.25	30
	0.3	40
	1.19	95
	1.75	100

LC-MS Method G

Column	Waters Atlantis dC18 100 x 2.1mm, 3μηι column 40 °C
Mobile phase	A - 0.1% Formic acid (water) B - 0.1% Formic acid (acetonitrile)
Flow rate	0.6 ml/min
Injection volume	3 pl
Detector	215nm (nominal)
Gradient	Time (mins)	%B
	0	5

145

ΙΟΟ

5.4	100
5.42	5

LC-MS Method H

Column	Atlantis dC18 2.1 x 50mm, 3Cm
Mobile phase	A = Formic acid (aq) 0.1% B = Formic acid (acetonitrile) 0.1%
Flow rate	1 ml/min
Injection volume	3 μΐ
Detector	215 nm (nominal)
Gradient	Time (mins)	%B
	0	5
	2.5	100
	2.7	100
	2.71	5
	3	5

LC-MS Method I

Column	Waters BEHC18 1.7pm , 2.1x50mm Ambient température
Mobile phase	A = Formic acid (aq) 0.1% B = Formic acid (acetonitrile) 0.1%
Flow rate	0.8 ml/min
Injection volume	3 μΐ

146

Detector	254 nm (nominal)
Gradient	Time (mins)	%B
	0	10
4.5	95
4.58	95

LC-MS Method J

Column	WatersBEHCl8 Ι.7μπι, 2.1x50mm Ambient température
Mobile phase	A = Formic acid (aq) 0.1% B = Formic acid (acetonitrile) 0.1%
Flow rate	0.8 ml/min
Injection volume	3μ1
Detector	254 nm (nominal)
Gradient	Time (mins)	%B
	0	10
1.19	95
1.7	95

Assessment of Biological Properties

l. Binding Assay:

Compounds are assessed for the ability to bind to FLAP in a binding assay that measures compound-specific dïsplacement of an iodinated (^l25I) FLAP inhibitor via a Scintillation Proximity Assay format (adapted from S. Charleson et al., Mol. PharmacoL, 1992, 41, 873-879).

147

Cell pellets produced from sf9 insect cells expressing recombinant human FLAP protein are resuspended in buffer A [15 mM Trîs-HCl (pH 7.5), 2 mM MgCl₂, 0.3 mM EDTA, l mM PMSF], The cells are lysed with a Dounce homogenizer and the material is centrifuged at 10,000 x g for 10 minutes. The supematant is then collected and centrifuged at 100,000 x g for 60 minutes. To préparé membrane protein for an assay, an aliquot of the 100,000 x g pellet is resuspended in 1 mi of buffer A, Dounce homogenized, and finally subjected to polytron mixing (30 seconds). Membrane protein (25 μΐ, 5 pg) îs mixed with WGA SPA beads (Amersham) and stirred for Ih. To an assay plate (Perkin Elmer FlexiPlate) is added 25 μΐ of test compound prepared in Binding buffer [100 mM Tris (pH 7.5), 140 mM NaCI, 5% glycerol, 2 mM EDTA, 0.5 mM TCEP, 0.05% Tween 20], 25 μΐ of [¹²⁵I]L-691,831 (an iodinated analog of MK.-591, Charleson et al. Mol. Pharmacol., 41, 873-879, 1992) and finally 50 μΐ of the bead/protein mixture, (final concentrations: beads, 200 pg/well; protein, 5pg/well; [¹²⁵I] probe, 0 08 nM/well(17 nCi/well). The plates are shaken for 2h before reading on a Mîcrobeta plate reader. Non-specific binding is determîned by the addition of 10 μΜ cold L-691,831 compound.

In general, the preferred potency range (IC50) of compounds in the above assay îs between 0.1 nM to 10 μΜ, the more preferred potency range is 0.1 nM to 1 μΜ, and the most preferred potency range is 0.1 nM to 100 nM.

2, Whole Blood Assay:

Compounds are additionally tested in a human whole blood assay to détermine their ability to inhibit the synthesis of LTB4 in a cellular system. Compounds are combined with heparinized human whole blood and incubated for 15 minutes at 37°C. Calcimycin (20μΜ final, prepared în phosphate-buffered saline, pH 7.4) is then added and the mixture is incubated for another 30 minutes at 37°C. The samples are centrifuged for 5 min at low speed (1500 x g) and the plasma layer is removed. Plasma LTB₄concentrations are then measured using an antibody-based homogenous time-resolved fluorescence method (CisBio, Bedford, MA).

148

In general, the preferred potency range (IC50) of compounds în the above assay is between ÎO nM to 10 μΜ, the more preferred potency range is 10 nM to 1 μΜ, and the most preferred potency range is 10 nM to 100 nM.

METHOD OF USE

The compounds of the invention are effective inhibitors of 5-lipoxygenase activating protein (FLAP) and thus inhibit leukotriene production. Therefore, in one embodiment of the invention, there is provided methods of treating leukotriene-mediated disorders using compounds of the invention. In another embodiment, there îs provided methods of treating cardiovascular, inflammatory, allergie, pulmonary and fibrotic diseases, rénal diseases and cancer using compounds of the invention.

Without wishing to be bound by theory, by inhibiting the activity of FLAP, the compounds of the invention block the production of LTs resulting from the oxidation of arachidonic acid by 5-LO and subséquent metabolism. Thus, the inhibition of FLAP activity îs an attractive means for preventing and treating a variety of diseases mediated by LTs. These include:

Cardiovascular diseases including atherosclerosis, myocardial infarction, stroke, aortic aneurysm, sickle cell crisis, ischemia-reperfusion injury, pulmonary arterial hypertension and sepsis;

Allergie diseases including asthma, allergie rhinitis, rhinosinusitis, atopie dermatitis and urticaria;

Fibrotic diseases including airway remodeling în asthma, idiopathic pulmonary fibrosis, scleroderma, asbestosis;

Pulmonary syndromes including adult respiratory distress syndrome, viral bronchiolitis, obstructive sleep apnea, chronic obstructive pulmonary disease, cystic fibrosis, and bronchopulmonary dysplasia;

149

Inflammatory diseases including rheumatoid arthritis, osteoarthritis, goût, glomerulonephritis, interstitial cystitis, psoriasis, inflammatory bowel disease, multiple sclerosis, inflammatory pain, systemic lupus erythematosus, transplant rejection, inflammatory and allergie ocular diseases;

Cancer including solid tumors, leukemias and lymphomas; and

Rénal diseases such as glomerulonephritis.

For treatment of the above-described diseases and conditions, a therapeutically effective dose will generally be in the range from about 0.01 mg to about 100 mg/kg of body weight per dosage of a compound ofthe invention; preferably, from about O.l mg to about 20 mg/kg of body weight per dosage. For example, for administration to a 70 kg person, the dosage range would be from about 0.7 mg to about 7000 mg per dosage of a compound of the invention, preferably from about 7.0 mg to about 1400 mg per dosage. Some degree of routine dose optimization may be required to détermine an optimal dosing level and pattern. The active ingrédient may be administered from 1 to 6 times a day.

General Administration and Pharmaceutical Compositions

When used as pharmaceuticals, the compounds of the invention are typically administered in the form of a pharmaceutical composition. Such compositions can be prepared using procedures well known in the pharmaceutical art and comprise at least one compound of the invention. The compounds of the invention may also be administered alone or in combination with adjuvants that enhance stability of the compounds of the invention, facilitate administration of pharmaceutical compositions containing them in certain embodiments, provide increased dissolution or dispersion, increased antagonist activity, provide adjunct therapy, and the like. The compounds according to the invention may be used on their own or in conjunction with other active substances according to the invention, optionally also in conjunction with other pharmacologically active substances. In general, the compounds of this invention are administered in a therapeutically or pharmaceutically effective amount, but may be administered in lower amounts for diagnostic or other purposes. kjY

150

Administration of the compounds of the invention, in pure form or in an appropriate pharmaceutical composition, can be carried out using any of the accepted modes of administration of pharmaceutical compositions. Thus, administration can be, for example, orally, buccally (e.g., sublingually), nasally, parenterally, topically, transdermally, vaginally, or rectally, in the form of solid, semi-sotid, lyophilized powder, or liquid dosage forms, such as, for example, tablets, suppositories, pills, soft elastic and hard gelatin capsules, powders, solutions, suspensions, or aérosols, or the like, preferably in unît dosage forms suitable for simple administration of précisé dosages. The pharmaceutical compositions will generally include a conventional pharmaceutical carrier or excipient and a compound of the invention as the/an active agent, and, in addition, may include other médicinal agents, pharmaceutical agents, carriers, adjuvants, diluents, vehicles, or combinations thereof. Such pharmaceutically acceptable excipients, carriers, or additives as well as methods of making pharmaceutical compositions for various modes or administration are well-known to those of skill in the art. The state of the art is evidenced, e.g., by Remington: The Science and Practice of Pharmacy, 20th Edition, A. Gennaro (ed.), Lippincott Williams & Wilkins, 2000; Handbook of Pharmaceutical Additives, Michael & Irene Ash (eds.), Gower, 1995; Handbook of Pharmaceutical Excipients, A.H. Kibbe (ed.), American Pharmaceutical Ass’n, 2000; H.C. Ansel and N .G. Popovish, Pharmaceutical Dosage Forms and Drug Delivery Systems, 5th ed., Lea and Febiger, 1990; each of which is incorporated herein by reference in their entiretîes to better describe the state of the art.

As one of skill in the art would expect, the forms of the compounds of the invention utilized in a particular pharmaceutical formulation will be selected (e.g., salts) that possess suitable physical characteristics (e.g., water solubility) that are required for the formulation to be efficacious. xjx/

Claims

wherein:

R^l and R² together with the carbon atom to which they are attached form a C3.10 carbocyclîc ring or a 5-l l membered heterocyclic ring, wherein each carbocycle or heterocycle is optionally independently substituted with one to two groups selected from C]_6 alkyl and halogen;

R³ is 5-11 membered heteroaryl ring contaîning one to three heteroatoms selected from nitrogen, oxygen and sulfur, wherein each R³ is optionally independently substituted with one to three groups selected from Cj.5 alkyl, Ci.5 alkoxy, Ci.3 alkylhydroxy, -CN, amino, Ci-3 alkylamino and C1.3 dialkylamino;

R⁴ is hydrogen, halogen, Ci.₃ alkyl or nitrile;

R⁵ is C].6 alkyl, C3.K} carbocycle, 5-l l membered heterocycle, aryl, 5-l 1 membered heteroaryl, -C(O)-R⁶ or-NR⁷R⁸, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R^iü and R¹¹ ; -a/

152

R⁶ is C3-8 heterocycle, amino, Ci_₃ alkylamîno, C].₃ dialkylamino or -NH-5-6 membered heterocycle, each optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R¹¹;

R and R are each independently hydrogen, -S(O)_nCi,_&alkyl or Ci_6 alkyl;

R⁹, R^lü and R¹¹ are independently selected from (a)-H, (b)-OH, (c) halogen, (d)-CN, (e) -CFj, (f) Ci^alkyl optionally substituted with one to three -OH, -N(R¹²)(Rⁱ³), aryl, -O-C1.2 alkyl-aryl, 3-6 membered heterocycle, -C(O)- 3-6 membered heterocycle, C|./,alkoxy , -S(O)_nC_walkyl, -CO₂R¹², halogen, -CN or-C(O)N(R^l2)(R¹³), (g) Cj.₆alkoxy, (h) -N(R^]2)(R¹³), (i) -S(O)_nCi.₆alkyl, (j) -CO₂R¹², (k) -C(O)N(R¹²)(R¹³), (l) -S(O)₂N(R^t2)(R¹³), (m) a 3-10 membered heterocyclic group optionally substituted with one to three groups selected from -OH, C|.₍, alkyl, Cj_6alkylhydroxy, C[._tlalkyl-CO₂R¹², -S(O)nCi. 6alkyl, oxo, -C(O)N(R¹²)(R¹³), and -CO2R¹², (n’) oxo, (o) -C(O)-C].₃ alkyl, (p) -C(O)-3-6 membered heterocycle optionally substituted with one to three groups selected from halogen hydroxy and Cj^alkoxy, (q) -OR¹², (r) 5-11 membered heteroaryl;

153

R¹² and R¹³ are each independently selected from -H, -C^alkyl, -C(O)-Ci.6 alkyl, C340 carbocycle and a 3-6 membered heterocyclic group, each of which is optionally independently substituted with one to three -OH, (Y, alkyl, C].6alkoxy, C(O)N(R^l4)(R¹⁵), -S(O)„Ci^alkyl, CN, C3.₁₀ carbocycle, -CO₂R¹⁴, CF₃, 3-6 membered heterocycle,halogen; or

R¹² and R¹³ together with the nitrogen atom to which they are attached form a heterocyclyl ring optionally substituted with one to three -OH, CN, Cj_6alkoxy or oxo;

R¹⁴ and R¹⁵ are each independently selected from -H and -C]^alkyl;

n is 0, 1 or 2;

or a pharmaceutically acceptable sait thereof.
2. A compound according to claim 1, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, 2.2.1 bicycloheptyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidînyl, tetrahydrothienyl, wherein each carbocycle or heterocycle is optionally independently substituted with one to two groups selected from CY alkyl and halogen;

R³ is pyridinyl, pyrimidinyl, pyrazinyl, pyrîdazînyl, pyrrolyl, imidazolyl, thienyl, furanyl or thiazolyl, wherein each R³ is optionally independently substituted with one to three groups selected from Cj_3 alkyl, Cm alkoxy, Cm alkylhydroxy, -CN, amino, Cm alkylamino and Cm dialkylamino;

R⁴ is hydrogen, halogen or methyl;

R⁵ is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert. butyl, pentyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, phenyl,

154 piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, pyrrolidinyl, tetrahydropyranyl, pyrrolyl, thienyl, furanyl, thiazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, triazolyl, dîhydropyridinyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quînolinyl, isoquînolinyl, indolyl, pyrrolopyridinyl, pyrrolopyrimidinyl, pyrazolopyrimidinyl, imidazopyridînyl, indazolyl, -C(O)-R⁶, hydroxy or -NR⁷R⁸, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R¹¹;

R⁶ is azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl, tetrahydropyranyl, morpholinyl, thiomorpholinyl, amino, Cj_3 alkylamino, C|.: dialkylamino or-NH-5-6 membered heterocycle, each optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R¹¹;

R⁷and R⁸ are each independently hydrogen, Ci.5 alkyl or -S(O)_nCj_₆alkyl;

R⁹, R¹⁰ and R^u are independently selected from (a)-H, (b)-OH, (c) halogen, (d)-CN, (e) -CFj, (f) Ci.₆alkyl optionally substituted with one to three -OH, -N(R¹²)(R¹³), phenyl, benzyl, phenethyl, azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, C(O)- 3-6 membered heterocycle, Ci_&alkoxy, -S(O)_nCi_6alkyl, -CO₂R¹², halogen, CN or -C(O)N(R^l2)(Rⁱ³), (g) Ci_₆alkoxy, (h) -N(R^]2)(R¹³), (i) -S(O)_nCi^alkyl, (j) -CO₂R¹², (k) -C(O)N(R^,2)(R^l3)>

(l) -S(O)₂N(R¹²)(R¹³), A

155 (m) oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, azetidinyl, pyrrolidinyl, tetrahydrothienyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl or thiomorpholinyldioxide, optionally substituted with one to three groups selected from -OH, Cj-6 alkyl, Ci.6alkylhydroxy, C[.6 alkyl-CO₂R¹², -S(O)nCi_6alkyl, oxo, C(O)N(R^I2)(R¹³), and-CO2R¹², (n’) oxo, (o) -C(O)-C].₃ alkyl, (p) -C(O)-3-6 membered heterocycle optionally substituted with one to three groups selected from halogen hydroxy and C'i ₆alkoxy, (q) -OR^]2, (r) imidazolyl, pyrrolyl, pyrazolyl, thienyl or furanyl;

R¹² and R¹³ are each independently selected from -H, -Cj^alkyl, -C(O)-C|.6 alkyl, cyclopropyl, cyclobutyl, cyclopentyl and a 3-6 membered heterocyclic group, each of which is optionally independently substituted with one to three -OH, Cjalkyl, Cj. 6alkoxy, -C(O)N(R^!4)(R^]5), -S(O)nCi.₆alkyl, CN, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, -CO₂R¹⁴, CF3, 3-6 membered heterocycle, halogen; or

R¹² and R¹³ together with the nitrogen atom to which they are attached form a heterocyclyl ring optionally substituted with one to three -OH, CN, Ci_6alkoxy or oxo;

R¹⁴ and R¹⁵ are each independently selected from -H and -C 1/.alkyl;

n is 0 or 2;

or a pharmaceutically acceptable sait thereof.
3. A compound according to claim 1 or 2, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl, cyclopentyl cyclohexyl, or tetrahydropyranyl wherein each carbocycle or heterocycle is optionally independently substituted with one to two groups selected from C1.3 alkyl and halogen;

156 or a pharmaceutically acceptable sait thereof.
4. A compound according to any of the claims l-3, wherein:

R³ is pyridinyl, pyrimidînyl, pyrazinyl or pyridazinyl, wherein each R³ is optionally independently substituted with one to three groups selected from C|.₃ alkyl, C].₃ alkoxy, C|.₃ alkylhydroxy, -CN, amino, Cj.₃ alkylamino and C].₃ dialkylamino;

or a pharmaceutically acceptable sait thereof.
5. A compound according to any of the claims l -4, wherein:

R⁵ is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert. butyl, pentyl, hexyl, phenyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholînyl, pyrrolidinyl, furanyl, thiazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, triazolyl, dihydropyridinyl, pyridinyl, pyrimidînyl, pyrazinyl, pyridazinyl, quinolinyl, isoquinolinyl, indolyl, pyrrolopyridinyl, pyrrolopyrimidinyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, -C(O)-R⁶, hydroxy or-NR⁷R⁸, wherein each R⁵ îs optionally independently substituted with one to three groups selected from R⁹, R^lû and Rⁿ;

R⁶ is azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, amino, C|.₃alkylamino orC^ dialkylamino;

R⁷and R⁸ are each independently hydrogen, Cj.₅ alkyl or -S(O)₂Ci.₆alkyl;

R⁹, R¹⁰ and R^u are independently selected from (a)-H, (b)-OH, (c) halogen, (d)-CN, (e) -CF₃, A

157 (f) C|.ί,alkyl optionally substituted with one to three -OH, -N(R^l2)(R¹³), phenyl, benzyi, phenethyl, azetidinyl, pyrrolidînyl, piperidinyl, piperazinyl, morpholinyl, C(O)- 3-6 membered heterocycle, Ci^alkoxy, -S(O)_nC].₆alkyl, -CO₂R¹², halogen, CN or -C(O)N(R¹²)(R¹³), (g) C].₆alkoxy, (h) -N(R^l2)(R¹³), (i) -S(O)₂C].₆alkyl, (j) -CO₂R¹², (k) -C(O)N(R^]2)(R¹³), (l) -S(O)₂N(R^l2)(R¹³), (m) oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, tetrahydrothienyl, azetidinyl, pyrrolidînyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl or thiomorpholinyldioxide, optionally substituted with one to three groups selected from -OH, Ci-₆alkyl, Ci.6alkylhydroxy, C|_₆ alkyl-CO₂R¹², -S(O)nCi.6alkyl, oxo, C(O)N(R^,2)(R¹³), and-CO2R¹², (n*) oxo, (0)-0(0)-0(.3 alkyl, (p) -C(O)-3-6 membered heterocycle optionally substituted with one to three groups selected from halogen hydroxy and Cj.6alkoxy, (q) -OR¹², (r) imidazolyl, pyrrolyl, pyrazolyl, thienyl or furanyl;

R¹² and R¹³ are each independently selected from -H, -Ci^alkyl, C(())-C| », alkyl, cyclopropyl, cyclobutyl, cyclopentyl and a 3-6 membered heterocyclic group, each of which is optionally independently substituted with one to three -OH, (Z, alkyl, C]. 6alkoxy, -C(O)N(R¹⁴)(R¹⁵), -S(O)nCi.₆alkyl, CN, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, --CO2R¹⁴, CF₃,3-6 membered heterocycle, halogen; or

R¹² and R¹³ together with the nitrogen atom to which they are attached form a heterocyclyl ring optionally substituted with one to three -OH, CN, C(.₆alkoxy or oxo; -γΥ''

158

R¹⁴ and R¹⁵ are each independently selected from -H and -Ci^alkyl;

n = 2;

or a pharmaceutically accepted sait thereof.
6. A compound according to claim 1 or 2, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl each optionally independently substituted with one to two groups selected from methyl and fluoro;

R³ is pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl, wherein each R³ is optionally independently substituted with one to three groups selected from methyl, -CN, -NH-CH3 and an amino group;

R⁴ is hydrogen;

R⁵ is phenyl, piperidinyl, piperazinyl, pyrrolidinyl, thiazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, triazolyl, dihydropyridinyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrazolopyrimidînyl, îmidazopyridinyl, indazolyl, or-NR⁷R⁸, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰and R¹¹;

R⁷and R⁸ are each independently hydrogen or C1.3 alkyl ;

R⁹, R¹⁰ and R^u are independently selected from (a)-H, (b)-OH, (c) halogen, (d)-CN, (e)-CF

159 (f) C i^alkyl optionally substituted with one to three-OH, -N(R^,2)(R^I3), phenyl, benzyl, phenethyl, azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, C(O)- 3-6 membered heterocycle, C)./,alkoxy, -S(O)_?(T ₆alkyl. -CO2R¹², halogen, CN or -C(O)N(R¹²)(R¹³), (g) Ci.₆alkoxy, (h) -N(R¹²)(R¹³), (i) -SiOhCrôalkyl, (j) -CO₂R¹², (k) -C(O)N(R^l2)(R¹³), (l) -S(O)₂N(R^]2)(R'³), (m) oxetanyl, tetrahydrothienyl, pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl or thiomorpholinyldioxide, optionally substituted with one to three groups selected from -OH, C]^alkyl, Ci-ftalkylhydroxy, C|_₆alkyl-CO₂R¹², -S(O)2Cj_ ftalkyl, oxo, -C(O)N(R^l2)(R¹³), and -CO2R¹², (n’) oxo, (o) -C(O)-C_w alkyl, (p) -C(O)-piperidînyl or -C(O)-pyrrolidinyl each optionally substituted with one to three groups selected from halogen hydroxy and Ci^alkoxy, (q) -OR¹², (r) imidazolyl, pyrrolyl or pyrazolyl;

R¹² and R¹³ are each independently selected from -H, -Cj^alkyl, -C(O)-Ci_6 alkyl, cyclopropyl, cyclobutyl, cyclopentyl and a 3-6 membered heterocyclic group, each of which is optionally independently substituted with one to three -OH, Ct_6 alkyl, Ct. 6alkoxy, -C(O)N(R^l4)(R¹⁵), -S(O)2Ci_6alkyl, CN, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, -CO₂R¹⁴, CF₃,3-6 membered heterocycle, halogen; or

R¹² and R¹³ together with the nitrogen atom to which they are attached form a heterocyclyl ring optionally substituted with one to three -OH, CN, C].₆alkoxy or oxo;

R¹⁴ and R¹⁵ are each independently selected from -H and -Ci.₆alkyl;

160 or a pharmaceutically accepted sait thereof.
7. A compound according to claim 6, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl;

or a pharmaceutically acceptable sait thereof.
8. A compound according to claim 6, wherein:

R¹ and R² together with the carbon atom to which they are attached is tetrahydropyranyl; or a pharmaceutically acceptable sait thereof.
9. A compound according to claim 6, wherein:

R³ is selected from or a pharmaceutically acceptable sait thereof.
10. A compound according to claim 6, wherein:

R^s is selected from imidazolyl, pyrazolyl, triazolyl, thîazolyl, oxazolyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, dihydropyridinyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolidinyl, and phenyl, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R^u;

or a pharmaceutically acceptable sait thereof.
11. A compound according to claim 6, wherein: \j</ ’

161

4 7 8 Ο 1Λ

R is-NR R , optionally substituted with one to three groups selected from R , R and or a pharmaceutically acceptable sait thereof.
12. A compound according to claim 6, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl ;

R³ is selected from

R⁴ is hydrogen;

R⁵ is selected from imidazolyl, pyrazolyl, triazolyl, thiazolyl, oxazolyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolidinyl, and phenyl, wherein each R⁵ is optionally independently substituted with one to three groups selected from R⁹, R¹⁰ and R¹¹;

or a pharmaceutically acceptable sait thereof.
13. A compound according to claim 6, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl;

R³ is selected from kaY^-

162

R⁴ is hydrogen ;

R⁵ is -NR⁷R^K optionally substituted with one to three groups selected from R⁹, R¹⁰ and R;

or a pharmaceutically acceptable sait thereof
14. A compound of formula IA:

IA wherein:

R¹ and R² together with the carbon atom to which they are attached form a C3.1Q carbocyclic ring or a 5-11 membered heterocyclic ring, wherein each carbocycle or heterocycle is optionally independently substituted with one to two groups selected from Ci-β alkyl and halogen;

R³ is 5-11 membered heteroaryl ring containing one to three heteroatoms selected from nitrogen, oxygen and sulfur, wherein each R³ is optionally independently substituted with one to three amino groups;

R⁴ is hydrogen, C/j alkyl or halogen; viX

163

R is 5-l l membered heteroaryl optionally independently substituted with one to three Ci-6 alkyl groups;

or a pharmaceutically acceptable sait thereof.
15. A compound of formula (IA) according to claim 14, wherein:

R and R together with the carbon atom to which they are attached is cyclopropyl, cyclobutyl, cyclopentyl, tetrahydrofuranyl, tetrahydropyranyl, wherein each carbocycle or heterocycle is optionally independently substituted with one to two groups selected from C]-5 alkyl and halogen;

R is pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, wherein each R is optionally independently substituted with one to three amino groups;

R⁴ is hydrogen;

R⁵ is pyrrolyl, thienyl, furanyl, thiazolyl, oxazolyl, isoxazolyl, pyrazolyl, imidazolyl, triazolyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quinolinyl, isoquinolinyl, indolyl, pyrrolopyridinyl, pyrrolopyrimîdinyl, pyrazolopyrimidinyl, imidazopyridinyl, indazolyl, wherein each R^s îs optionally substituted with one to three CY alkyl groups; or a pharmaceutically acceptable sait thereof.
16. A compound of formula (IA) according to claim 14 or 15, wherein:

R¹ and R² together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl;

or a pharmaceutically acceptable sait thereof.
17. A compound of formula (IA) according to claim 14-16, wherein:

R³ is pyrimidinyl substituted with an amino group;

164 or a pharmaceutically acceptable sait thereof.
18. A compound of formula (IA) according to claim 14 -17, wherein:

R⁵ is pyrazolyl or, pyridinyl, each optionally substituted with one to three Ct.₃ alkyl groups;

or a pharmaceutically acceptable sait thereof.
19. A compound of formula (IA) according to claim 14 or 15, wherein:

j 2

R and R together with the carbon atom to which they are attached is cyclobutyl or tetrahydropyranyl ;

R³ is pyrimidinyl substituted with an amino group;

R⁴is H

R⁵ is pyrazolyl or, pyridinyl, each optionally substituted with one to three methyl groups; or a pharmaceutically acceptable sait thereof.
20. A compound selected from the group consisting of: