Compounds and methods for inhibiting JAK
Disclosed are compounds of formula (I), pharmaceutical compositions comprising such compounds and methods/uses of using the same, for example, for treating a JAK-related disorder, such as cancer, cancer cachexia or an immune disorder: wherein R 1 is methyl or ethyl; R 2 is selected from methyl, ethyl, methoxy and ethoxy; R 3 is selected from hydrogen, chlorine, fluorine, bromine and methyl; R 4 is selected from methyl, ethyl and —CH 2 OCH 3 ; R 5 and R 6 are each individually methyl or hydrogen; and R 7 is selected from methyl, ethyl, —(CH 2 ) 2 OH and —(CH 2 ) 2 OCH 3 , or a pharmaceutically acceptable salt thereof.
1. A solvate form of compound of (2R)—N-(3-{2-[(3-methoxy-1-methyl-1H-pyrazol-4-yl)amino]pyrimidin-4-yl}-1H-indol-7-yl)-2-(4-methylpiperazin-1-yl)propanamide, or a pharmaceutically acceptable salt thereof.
2. The solvate form of claim 1 , which is hemi-toluene solvate form or hemi-EtOAc solvate form.
3. The solvate form of claim 2 , which has a crystalline structure.
4. The solvate form of claim 1 , which is hemi-toluene solvate form of (2R)—N-(3-{2-[(3-methoxy-1-methyl-1H-pyrazol-4-yl)amino]pyrimidin-4-yl}-1H-indol-7-yl)-2-(4-methylpiperazin-1-yl)propanamide.
5. The solvate form of claim 1 , which is hemi-EtOAc solvate form of (2R)—N-(3-{2-[(3-methoxy-1-methyl-1H-pyrazol-4-yl)amino]pyrimidin-4-yl}-1H-indol-7-yl)-2-(4-methylpiperazin-1-yl)propanamide.
6. The compound of claim 5 , which has an X-ray powder diffraction (XRPD) pattern comprising at least one, two or three specific peaks expressed as 2θ (±0.2°) selected from the peaks listed in Table 20.
7. The solvate form of claim 5 , which has an XRPD pattern comprising at least one specific peak expressed as 2θ (±0.2°) selected from 18.6°, 24.1°, 25.8°, 28.9°, 32.1°, 33.0°, 36.5° and 38.9°.
8. The solvate form of claim 5 , which has an XRPD pattern comprising at least three specific peaks expressed as 2θ (±0.2°) selected from 18.6°, 24.1°, 25.8°, 28.9°, 32.1°, 33.0°, 36.5° and 38.9°.
9. The solvate form of claim 5 , which has an XRPD pattern comprising peaks expressed as 2θ (±0.2°)=18.6°, 24.1°, 25.8°, 28.9°, 32.1°, 33.0°, 36.5° and 38.9°.
10. The solvate form of claim 5 , which has an XRPD pattern substantially similar to FIG. 7 .
11. The solvate form of claim 5 , which has a DSC thermogram comprising an endotherm with a desolvation onset at about 116° C. and a peak at about 119° C.
12. The solvate form of claim 5 , which has a TGA thermogram exhibiting a mass loss of about 8.0% upon heating from about 25° C. to about 200° C.
13. The solvate form of claim 5 , which has a TGA thermogram substantially similar to FIG. 8 .
14. The compound of claim 4 , which has an XRPD pattern comprising at least one, two or three specific peaks expressed as 2θ (±0.2°) selected from the peaks listed in Table 18.
15. The solvate form of claim 4 which has an XRPD pattern comprising at least one specific peak expressed as 2θ (±0.2°) selected from 16.3°, 23.9°, 24.4°, 25.1°, 28.1°, 29.3°, 31.8°, 32.7° and 37.5°.
16. The solvate form of claim 4 , which has an XRPD pattern comprising at least three specific peaks expressed as 2θ (±0.2°) selected from 16.3°, 23.9°, 24.4°, 25.1°, 28.1°, 29.3°, 31.8°, 32.7°, 37.5°.
17. The solvate form of claim 4 , which has an XRPD pattern comprising at least peaks expressed as 2θ (±0.2°)=16.3°, 23.9°, 24.4°, 25.1°, 28.1°, 29.3°, 31.8°, 32.7° and 37.5°.
18. The solvate form of claim 4 , which has an XRPD pattern substantially similar to FIG. 3 .
19. The solvate form of claim 4 , which has a DSC thermogram comprising an endotherm with a desolvation onset at about 112° C. and a peak at about 117° C.
20. The solvate form of claim 4 which has a TGA thermogram exhibiting a mass loss of about 10.0% upon heating from about 25° C. to about 200° C.
21. The solvate form of claim 4 , which has a TGA thermogram substantially similar to FIG. 4 .
22. A pharmaceutical composition, which comprises the solvate form of claim 1 and a pharmaceutically acceptable carrier, diluent or excipient.