Thiazolecarboxamides and pyridinecarboxamide compounds useful as Pim kinase inhibitors
The present disclosure describes thiazole and pyridine carboxamide derivatives, their compositions and methods of use. The compounds inhibit the activity of the Pim kinases and are useful in the treatment of diseases related to the activity of Pim kinases including, e.g., cancer and other diseases.
1. A method of treating a solid tumor comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound, wherein the compound is selected from:
N-{4-[3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide;
N-{4-[(3R,4R,5S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide;
N-{4-[(3R,4R,5S,7R)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide; and
N-{4-[(3R,4R,5S,7S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide;
or a pharmaceutically acceptable salt thereof,
wherein the solid tumor is colon cancer, esophageal cancer, renal cancer, hepatic cancer, gastric cancer, breast cancer, lung cancer, a cancer of the head or neck, or bladder cancer.
2. The method of claim 1 , wherein the compound is N-{4-[3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide, or a pharmaceutically acceptable salt thereof.
3. The method of claim 1 , wherein the compound is N-{4-[(3R,4R,5S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide, or a pharmaceutically acceptable salt thereof.
4. The method of claim 1 , wherein the compound is N-{4-[(3R,4R,5S,7R)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide, or a pharmaceutically acceptable salt thereof.
5. The method of claim 1 , wherein the compound is N-{4-[(3R,4R,5S,7S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide, or a pharmaceutically acceptable salt thereof.
6. The method of claim 1 , wherein the solid tumor is esophageal cancer.
7. The method of claim 1 , wherein the solid tumor is a cancer of the head or neck.
8. A method of treating a hematological cancer comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound, wherein the compound is selected from:
N-{4-[3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide;
N-{4-[(3R,4R,5S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamine;
N-{4-[(3R,4R,5S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide; and
N-{4-[(3R,4R,5S,7S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide;
or a pharmaceutically acceptable salt thereof,
wherein the hematological cancer is acute lymphoblastic leukemia (ALL), chronic lymphocytic leukemia (CLL), mantle cell lymphoma, non-Hodgkin lymphoma, or Hodgkin lymphoma.
9. The method of claim 8 , wherein the compound is N-{4-[3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide, or a pharmaceutically acceptable salt thereof.
10. The method of claim 8 , wherein the compound is N-{4-[(3R,4R,5S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide, or a pharmaceutically acceptable salt thereof.
11. The method of claim 8 , wherein the compound is N-{4-[(3R,4R,5S,7R)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide, or a pharmaceutically acceptable salt thereof.
12. The method of claim 8 , wherein the compound is N-{4-[(3R,4R,5S,7S)-3-amino-4-hydroxy-5-methylpiperidin-1-yl]-7-hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-3-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide, or a pharmaceutically acceptable salt thereof.
13. The method of claim 8 , wherein the hematological cancer is mantle cell lymphoma.
14. The method of claim 1 , wherein the solid tumor is colon cancer.
15. The method of claim 1 , wherein the solid tumor is renal cancer.
16. The method of claim 1 , wherein the solid tumor is hepatic cancer.
17. The method of claim 16 , wherein the hepatic cancer is hepatocellular cancer.
18. The method of claim 1 , wherein the solid tumor is gastric cancer.
19. The method of claim 1 , wherein the solid tumor is breast cancer.
20. The method of claim 1 , wherein the solid tumor is lung cancer.
21. The method of claim 1 , wherein the solid tumor is bladder cancer.
22. The method of claim 8 , wherein the hematological cancer is acute lymphoblastic leukemia (ALL).
23. The method of claim 8 , wherein the hematological cancer is chronic lymphocytic leukemia (CLL).
24. The method of claim 8 , wherein the hematological cancer is non-Hodgkin lymphoma.
25. The method of claim 24 , wherein the non-Hodgkin lymphoma is relapsed non-Hodgkin lymphoma, refractory non-Hodgkin lymphoma, or recurrent follicular non-Hodgkin lymphoma.
26. The method of claim 8 , wherein the hematological cancer is Hodgkin lymphoma.