Fused heterocyclic compounds as selective BMP inhibitors
US-10196392-B2 · Feb 5, 2019 · US
US10745400B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10745400-B2 |
| Application number | US-201916353745-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 14, 2019 |
| Priority date | Mar 14, 2018 |
| Publication date | Aug 18, 2020 |
| Grant date | Aug 18, 2020 |
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Provided herein are substituted imidazo[1,2-a]pyridines useful as inhibitors of BMP signaling. The invention further provides pharmaceutical compositions of the compounds of the invention. The invention also provides medical uses of substituted imidazo[1,2-a]pyridines.
Opening claim text (preview).
What is claimed is: 1. A compound having a structure of Formula I or a pharmaceutically acceptable salt thereof: wherein R 1 and R 2 are each independently H or halo; A is X 1 is O or NH; X 2 is CR 4 R 5 or —CH 2 CH 2 —; X 3 is CR 8 R 9 or NH; R 3 , R 4 , and R 5 are each independently H or alkyl, or R 4 and R 5 combine to form an optionally substituted 4-, 5-, or 6-membered ring; R 6 and R 7 combine to form an optionally substituted 4-, 5-, or 6-membered ring; and R 8 and R 9 are each independently H or alkyl, or R 8 and R 9 combine to form an optionally substituted 4-, 5-, or 6-membered ring. 2. The compound of claim 1 , wherein R 1 is F and R 2 is F. 3. The compound of claim 1 , wherein X 1 is O. 4. The compound of claim 1 , wherein X 1 is NH. 5. The compound of claim 1 , wherein R 4 and R 5 combine to form an optionally substituted 5 or 6-membered ring. 6. The compound of claim 1 , wherein X 3 is NH. 7. The compound of claim 1 , wherein R 6 and R 7 combine to form an optionally substituted 4- or 5-membered ring. 8. The compound of claim 1 , wherein R 8 and R 9 combine to form an optionally substituted 4-, 5- or 6-membered ring. 9. The compound of claim 1 , wherein A is 10. A compound having the structure of Formula II or a pharmaceutically acceptable salt thereof: wherein G is and J is selected from optionally substituted heteroaryl or 11. The compound of claim 10 , wherein G is 12. The compound of claim 10 , wherein J is 13. The compound of claim 10 , wherein J is 14. A compound selected from: or a pharmaceutically acceptable salt thereof. 15. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier. 16. A pharmaceutical composition comprising a compound of claim 10 and a pharmaceutically acceptable carrier. 17. A pharmaceutical composition comprising a compound of claim 14 and a pharmaceutically acceptable carrier.
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