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 myeloproliferative disorder 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-methylpiperidin1-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 myeloproliferative disorder is polycythemia vera (PV), essential thrombocythemia (ET), primary myelofibrosis (PMF), myelofibrosis with myeloid metaplasia (MMM), post-polycythemia vera/essential thrombocythemia myelofibrosis (Post-PV/ET MF), post-essential thrombocythemia myelofibrosis (Post-ET MF) or post-polycythemia vera myelofibrosis (Post-PV MF).
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 myeloproliferative disorder is polycythemia vera (PV).
7. The method of claim 1 , wherein the myeloproliferative disorder is essential thrombocythemia (ET).
8. The method of claim 1 , wherein the myeloproliferative disorder is primary myelofibrosis (PMF).
9. The method of claim 1 , wherein the myeloproliferative disorder is myelofibrosis with myeloid metaplasia (MMM).
10. The method of claim 1 , wherein the myeloproliferative disorder is post-polycythemia vera/essential thrombocythemia myelofibrosis (Post-PV/ET MF).
11. The method of claim 1 , wherein the myeloproliferative disorder is post-essential thrombocythemia myelofibrosis (Post-ET MF).
12. The method of claim 1 , wherein the myeloproliferative disorder is post-polycythemia vera myelofibrosis (Post-PV MF).
13. A method of treating a myeloproliferative disorder comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound, wherein the compound is N-{4-[(3R,4R,5S,7R)-3-amino-4-hydroxy-5-methylpiperidin-l-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 myeloproliferative disorder is polycythemia vera (PV), essential thrombocythemia (ET), primary myelofibrosis (PMF), myelofibrosis with myeloid metaplasia (MMM), post-polycythemia vera/essential thrombocythemia myelofibrosis (Post-PV/ET MF), post-essential thrombocythemia myelofibrosis (Post-ET MF) or post-polycythemia vera myelofibrosis (Post-PV MF).
14. The method of claim 13 , wherein the myeloproliferative disorder is polycythemia vera (PV).
15. The method of claim 13 , wherein the myeloproliferative disorder is essentia thrombocythemia (ET).
16. The method of claim 13 , wherein the myeloproliferative disorder is primary myelofibrosis (PMF).
17. The method of claim 13 , wherein the myeloproliferative disorder is myelofibrosis with myeloid metaplasia (MMM).
18. The method of claim 13 , wherein the myeloproliferative disorder is post- polycythemia vera/essential thrombocythemia myelofibrosis (Post-PV/ET MF).
19. The method of claim 13 , wherein the myeloproliferative disorder is post-essential thrombocythemia myelofibrosis (Post-ET MF).
20. The method of claim 13 , wherein the myeloproliferative disorder is post- polycythemia vera myelofibrosis (Post-PV MF).