Heterocyclic amides as kinase inhibitors
Disclosed are compounds having the formula: wherein R 1 , R 2 , and R 3 are as defined herein, and methods of making and using the same.
1. A method of alleviating or mitigating a neurological disease or disorder 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.
2. The method of claim 1 , wherein the neurological disease or disorder is traumatic brain injury.
3. The method of claim 1 , wherein the neurological disease or disorder is stroke.
4. The method of claim 1 , wherein the neurological disease or disorder is multiple sclerosis.
5. The method of claim 1 , wherein the neurological disease or disorder is Alzheimer's disease.
6. The method of claim 1 , wherein the neurological disease or disorder is Parkinson's disease.
7. The method of claim 1 , wherein the neurological disease or disorder is amyotrophic lateral sclerosis.
8. A method of alleviating or mitigating a neurological disease or disorder in a human in need thereof comprising administering to the human a therapeutically effective amount of a compound according to Formula (I) which is (S)-1-(4-(5-(3,5-difluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbonyl)piperidin-1-yl)ethanone:
or a pharmaceutically acceptable salt thereof.
9. The method of claim 8 , wherein the neurological disease or disorder is traumatic brain injury.
10. The method of claim 8 , wherein the neurological disease or disorder is stroke.
11. The method of claim 8 , wherein the neurological disease or disorder is multiple sclerosis.
12. The method of claim 8 , wherein the neurological disease or disorder is Alzheimer's Disease.
13. The method of claim 8 , wherein the neurological disease or disorder is Parkinson's Disease.
14. The method of claim 8 , wherein the neurological disease or disorder is amyotrophic lateral sclerosis.
15. A method of alleviating or mitigating a gastrointestinal inflammation disease or condition 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 a pharmaceutically acceptable salt thereof,
provided the compound is not:
cyclohexyl(5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)methanone.
16. The method of claim 15 , wherein the gastrointestinal inflammation disease or condition is inflammatory bowel disease.
17. The method of claim 16 , wherein the inflammatory bowel disease is Crohn's disease or ulcerative colitis.
18. A method of alleviating or mitigating an inflammatory bowel disease in a human in need thereof comprising administering to the human a therapeutically effective amount of a compound according to Formula (I) which is (S)-1-(4-(5-(3,5-difluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbonyl)piperidin-1-yl)ethanone:
or a pharmaceutically acceptable salt thereof.
19. The method of claim 18 , wherein the inflammatory bowel disease is Crohn's disease.
20. The method of claim 18 , wherein the inflammatory bowel disease is ulcerative colitis.
21. A method of alleviating or mitigating a neurological disease or disorder in a human in need thereof comprising administering to the human a therapeutically effective amount of a compound according to Formula (I) which is (S)-1-(4-(5-(3,5-difluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbonyl)piperidin-1-yl)ethanone:
22. The method of claim 21 , wherein the neurological disease or disorder is traumatic brain injury.
23. The method of claim 21 , wherein the neurological disease or disorder is stroke.
24. The method of claim 21 , wherein the neurological disease or disorder is multiple sclerosis.
25. The method of claim 21 , wherein the neurological disease or disorder is Alzheimer's Disease.
26. The method of claim 21 , wherein the neurological disease or disorder is Parkinson's Disease.
27. The method of claim 21 , wherein the neurological disease or disorder is amyotrophic lateral sclerosis.
28. A method of alleviating or mitigating an inflammatory bowel disease in a human in need thereof comprising administering to the human a therapeutically effective amount of a compound according to Formula (I) which is (S)-1-(4-(5-(3,5-difluorophenyl)-4,5-dihydro-1H-pyrazole-1-carbonyl)piperidin-1-yl)ethanone:
29. The method of claim 28 , wherein the inflammatory bowel disease is Crohn's disease.
30. The method of claim 28 , wherein the inflammatory bowel disease is ulcerative colitis.