Solid forms of (R)-N-(2-(5-fluoropyridin-3-yl)-8-isopropylpyrazolo[ 1,5-a][1,3,5]triazin-4-yl)-2,3,4,9-tetrahydro-1H-carbazol-3-amine maleate as aryl hydrocarbon receptor (AHR) inhibitors
The present invention provides solid forms of (R)—N-(2-(5-fluoropyridin-3-yl)-8-isopropylpyrazolo[1,5-a][1,3,5]triazin-4-yl)-2,3,4,9-tetrahydro-1H-carbazol-3-amine maleate (Compound 2) represented by the formula:
1. A compound represented by formula 2:
wherein 1≤X≤2.
2. A pharmaceutical composition comprising the compound according to claim 1 and a pharmaceutically acceptable carrier or excipient.
3. A method for inhibiting aryl hydrocarbon receptor (AHR) activity in a biological sample, wherein the method comprises contacting the biological sample with the compound according to claim 1 .
4. A method for inhibiting aryl hydrocarbon receptor (AHR) activity in a patient in need thereof, wherein the method comprises administering to the patient a therapeutically effective amount of the compound according to claim 1 .
5. The method according to claim 4 , wherein the patient has an AHR-mediated disorder selected from the group consisting of a cancer and an inflammatory disorder.
6. The method according to claim 5 , wherein the cancer is selected from the group consisting of acute myeloid leukemia, bladder cancer, esophageal cancer, head and neck squamous cell carcinoma, kidney cancer, leukemia, lung cancer, melanoma, ovarian cancer, and stomach cancer.
7. A process for preparing a compound represented by formula 2 according to claim 1 :
wherein 1≤X≤2;
wherein the process comprises the following step:
combining a compound represented by formula A:
with maleic acid represented by the following formula:
optionally in the presence of a solvent.
8. The process according to claim 7 , wherein the process further comprises combining the compound represented by formula A and maleic acid in a stoichiometric ratio of 2:1.
9. A crystal form of a compound represented by formula 2:
wherein the crystal form is crystal Form A; and
wherein crystal Form A is characterized by an X-ray powder diffraction pattern comprising at least one characteristic peak at an angle (°2θ) selected from the group consisting of 5.3°±0.2°2θ, 11.3°±0.2°2θ, and 16.0°±0.2°2θ.
10. The crystal form according to claim 9 , wherein the crystal form is further characterized by an X-ray powder diffraction pattern comprising at least two characteristic peaks at angles (°2θ) selected from the group consisting of 5.3°±0.2°2θ, 11.3°±0.2°2θ, and 16.0°±0.2°2θ.
11. The crystal form according to claim 9 , wherein the crystal form is further characterized by an X-ray powder diffraction pattern comprising three characteristic peaks at angles (°2θ) of 5.3°±0.2°2θ, 11.3°±0.2°2θ, and 16.0°±0.2°2θ.
12. The crystal form according to claim 9 , wherein the crystal form is further characterized by an X-ray powder diffraction pattern as depicted in FIG. 8 .
13. The crystal form according to claim 9 , wherein the crystal form is further characterized by a thermogravimetry/differential thermal analysis trace as depicted in FIG. 9 .
14. A pharmaceutical composition comprising the crystal form according to claim 9 and a pharmaceutically acceptable carrier or excipient.
15. A method for inhibiting aryl hydrocarbon receptor (AHR) activity in a biological sample, wherein the method comprises contacting the biological sample with the crystal form according to claim 9 .
16. A method for inhibiting aryl hydrocarbon receptor (AHR) activity in a patient in need thereof, wherein the method comprises administering to the patient a therapeutically effective amount of the crystal form according to claim 9 .
17. The method according to claim 16 , wherein the patient has an AHR-mediated disorder selected from the group consisting of a cancer and an inflammatory disorder.
18. The method according to claim 17 , wherein the cancer is selected from the group consisting of acute myeloid leukemia, bladder cancer, esophageal cancer, head and neck squamous cell carcinoma, kidney cancer, leukemia, lung cancer, melanoma, ovarian cancer, and stomach cancer.
19. A process for preparing the crystal form of a compound represented by formula 2 according to claim 9 :
wherein the crystal form is crystal Form A; and
wherein crystal Form A is characterized by an X-ray powder diffraction pattern comprising at least one characteristic peak at an angle (°2θ) selected from the group consisting of 5.3°±0.2°2θ, 11.3°±0.2°2θ, and 16.0°±0.2°2θ;
wherein the process comprises the following step:
combining a compound represented by formula A:
with maleic acid represented by the following formula:
optionally in the presence of a solvent.