Furo- and thieno-pyridine carboxamide compounds useful as pim kinase inhibitors
US-9556197-B2 · Jan 31, 2017 · US
US9862705B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9862705-B2 |
| Application number | US-201615260695-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 9, 2016 |
| Priority date | Sep 9, 2015 |
| Publication date | Jan 9, 2018 |
| Grant date | Jan 9, 2018 |
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The present invention relates to salt forms of the Pim kinase inhibitor N-{(7R)-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, including methods of preparation thereof, and intermediates in the preparation thereof, where the compound is useful in the treatment of Pim kinase-related diseases such as cancer.
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What is claimed is: 1. A salt having the formula: 2. The salt of claim 1 wherein the salt is crystalline. 3. The salt of claim 2 which is hydrated. 4. The salt of claim 3 which is a hemihydrate. 5. A pharmaceutical composition comprising the salt of claim 1 and at least one pharmaceutically acceptable carrier. 6. A solid oral dosage form comprising the pharmaceutical composition of claim 5 . 7. A pharmaceutical composition comprising the salt of claim 2 and at least one pharmaceutically acceptable carrier. 8. A solid oral dosage form comprising the pharmaceutical composition of claim 7 . 9. A pharmaceutical composition comprising the salt of claim 3 and at least one pharmaceutically acceptable carrier. 10. A solid oral dosage form comprising the pharmaceutical composition of claim 9 . 11. A pharmaceutical composition comprising the salt of claim 4 and at least one pharmaceutically acceptable carrier. 12. A solid oral dosage form comprising the pharmaceutical composition of claim 11 .
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