Heterocyclic amides as kinase inhibitors

Abstract

Disclosed are compounds having the formula:wherein R1, R2, and R3 are as defined herein, and methods of making and using the same.

1 - 26 . (canceled) 
     
     
         27 . A method of multiple sclerosis therapy in a human in need thereof, comprising administering to the human a therapeutically effective amount of a compound according to Formula (I): 
       
         
           
           
               
               
           
         
       
       wherein:
 R 1  is (C 1 -C 4 )alkoxy-CH 2 —, phenyl(C 1 -C 4 )alkoxy-CH 2 —, or a substituted or unsubstituted (C 2 -C 4 )alkynyl, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkyl-(C 1 -C 4 )alkyl-group, or a substituted or unsubstituted 5-6 membered heterocycloalkyl group further optionally substituted by halogen or (C 1 -C 4 )alkyl,
 wherein said substituted (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkyl-alkyl-, or 5-6 membered heterocycloalkyl group is substituted by 1, 2 or 3 substituents independently selected from hydroxyl, ((benzyloxy)carbonyl)amino, cyano, halogen, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )alkyl-CO—, cyano(C 1 -C 4 )alkyl-CO—, (C 1 -C 4 )alkoxy-(C 1 -C 4 )alkyl-CO—, (C 1 -C 4 )alkoxy-CO—, (C 1 -C 4 )alkylNHCO—, ((C 1 -C 4 )alkyl)((C 1 -C 4 )alkyl)NCO—, halo(C 1 -C 4 )alkyl-CO—, optionally substituted (C 3 -C 6 )cycloalkyl-CO—, optionally substituted (C 3 -C 6 )cycloalkyl-(C 1 -C 4 )alkyl-CO—, optionally substituted phenyl-CO—, optionally substituted phenyl-SO 2 —, optionally substituted phenyl(C 1 -C 4 )alkyl-CO—, optionally substituted 5-6 membered heteroaryl-CO—, and optionally substituted 9-10 membered heteroaryl-CO—,
 wherein said optionally substituted (C 3 -C 6 )cycloalkyl-CO—, optionally substituted (C 3 -C 6 )cycloalkyl-(C 1 -C 4 )alkyl-CO—, optionally substituted phenyl-CO—, optionally substituted phenyl-SO 2 —, optionally substituted phenyl(C 1 -C 4 )alkyl-CO—, optionally substituted 5-6 membered heteroaryl-CO—, or optionally substituted 9-10 membered heteroaryl-CO— is optionally substituted by 1 or 2 substituents independently selected from halogen, cyano, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )alkyl-CO—, halo(C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl-CO—, (C 3 -C 6 )cycloalkyl and 5-6 membered heterocycloalkyl; or 
 
 said substituted (C 2 -C 4 )alkynyl, (C 3 -C 6 )cycloalkyl or 5-6 membered heterocycloalkyl group is substituted by an optionally substituted phenyl, 5-6 membered heteroaryl or 9-membered heteroaryl group,
 wherein said phenyl, 5-6 membered heteroaryl or 9-membered heteroaryl group is optionally substituted by 1 or 2 substituents independently selected from halogen, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-CO—, halo(C 1 -C 4 )alkyl, and halo(C 1 -C 4 )alkyl-CO—; 
 
 
 R 2  is a substituted or unsubstituted phenyl, (C 3 -C 6 )cycloalkyl, 5-6 membered oxygen-containing heterocycloalkyl, 5-6 membered heteroaryl, 9-membered heteroaryl, 9-10 membered carbocyclic-aryl, or 9-10 membered heterocyclic-aryl group,
 wherein said substituted phenyl, (C 3 -C 6 )cycloalkyl, 5-6 membered heterocycloalkyl, 5-6 membered heteroaryl, 9-membered heteroaryl, 9-10 membered carbocyclic-aryl, or 9-10 membered heterocyclic-aryl group is substituted by 1, 2 or 3 substituents independently selected from halogen, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, halo(C 1 -C 4 )alkoxy, and cyano; 
 
 R 3  is H or halogen; 
 or pharmaceutically acceptable salt thereof, 
 provided the compound is not:
 cyclohexyl(5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)methanone. 
 
 
     
     
         28 . A method of multiple sclerosis therapy in a human in need thereof, comprising administering to the human a therapeutically effective amount of a compound according to Formula (I) which is (5)-1-(4-(5-(3,5-difluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbonyl)piperidin-1-yl)ethanone: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof. 
     
     
         29 . The method of  claim 28 , wherein the method comprises administering to the human a therapeutically effective amount of (S)-1-(4-(5-(3,5-difluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbonyl)piperidin-1-yl)ethanone: