Crystal form of casein kinase 1ϵ inhibitor and preparation method and use thereof
The present disclosure discloses a crystal form of a casein kinase 1ε inhibitor and a preparation method and use of the crystal form. Specifically, the present disclosure relates to a crystal form of the compound (S)-2-(1-(4-amino-3-(2,3-difluoro-4-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-5-chloro-3-phenylquinazoline-4(3H)one methanesulfonate and a preparation method and use of the crystal form. The crystal form of the casein kinase 1ε inhibitor compound of the present disclosure has good water solubility and oral absorption, and can be better used for the treatment of malignant tumors and autoimmune diseases that benefit from the inhibition of casein kinase 1ε activity.
1 . A crystal form A of a casein kinase 1c inhibitor as shown in a formula (I), wherein the crystal form A has characteristic peaks in an X-ray powder diffraction pattern when a 2θ value is 7.848±0.2°, 11.618±0.2°, 15.562±0.2°, 15.853±0.2°, 20.185±0.2° and 25.655±0.2°:
2 . A method for preparing the crystal form A according to claim 1 , comprising: heating the compound as shown in the formula (I) for dissolution in a solvent I, conducting heat filtration optionally, and conducting cooling crystallization on a resulting dissolved clarification solution to obtain the crystal form A, wherein the solvent I is selected from acetone, 1,4-dioxane, tetrahydrofuran/isopropanol, tetrahydrofuran/acetone, tetrahydrofuran/ethyl acetate and 1,4-dioxane/isopropanol.
3 . A crystal form B of the compound as shown in the formula (I), wherein the crystal form B has characteristic peaks in an X-ray powder diffraction pattern when a 2θ value is 10.739±0.2°, 11.961±0.2°, 13.726±0.2°, 14.374±0.2°, 23.714±0.2°, 24.057±0.2° and 25.033±0.2°:
4 . A method for preparing the crystal form B according to claim 3 , comprising: dissolving the compound as shown in the formula (I) in a solvent II at room temperature, and conducting standing for volatilization crystallization to obtain the crystal form B, wherein the solvent II is selected from tetrahydrofuran, butanone, acetonitrile/methyl tert-butyl ether and butanone/acetone.
5 . A crystal form C of the compound as shown in the formula (I), wherein the crystal form C has characteristic peaks in an X-ray powder diffraction pattern when a 2θ value is 7.319±0.2°, 8.092±0.2°, 11.763±0.2°, 14.728±0.2°, 15.855±0.2° and 16.265±0.2°:
6 . A method for preparing the crystal form C according to claim 5 , comprising: heating the compound as shown in the formula (I) for dissolution in a solvent III, conducting heat filtration optionally, and conducting cooling crystallization on a resulting dissolved clarification solution to obtain the crystal form C, wherein the solvent III is selected from methyl isobutyl ketone.
7 . A crystal form D of the compound as shown in the formula (I), wherein the crystal form D has characteristic peaks in an X-ray powder diffraction pattern when a 2θ value is 11.308±0.2°, 17.237±0.2°, 18.568±0.2°, 20.213±0.2°, 21.148±0.2° and 21.293±0.2°:
8 . A method for preparing the crystal form D according to claim 7 , comprising: heating the compound as shown in the formula (I) for dissolution in a solvent IV, conducting heat filtration optionally, and conducting cooling crystallization on a resulting dissolved clarification solution to obtain the crystal form D, wherein the solvent IV is selected from methanol/isopropanol.
9 . A crystal form E of the compound as shown in the formula (I), wherein the crystal form E has characteristic peaks in an X-ray powder diffraction pattern when a 2θ value is 7.114±0.2°, 7.936±0.2°, 9.973±0.2°, 11.040±0.2°, 14.484±0.2°, 15.504±0.2°, 16.507±0.2°, 20.071±0.2° and 21.555±0.2°:
10 . A method for preparing the crystal form E according to claim 9 , comprising: heating the compound as shown in the formula (I) for dissolution in a solvent V, conducting heat filtration optionally, and conducting cooling crystallization on a resulting dissolved clarification solution to obtain the crystal form E, wherein the solvent V is selected from 1,4-dioxane/ethyl acetate.
11 . A crystal form F of the compound as shown in the formula (I), wherein the crystal form F has characteristic peaks in an X-ray powder diffraction pattern when a 2θ value is 9.959±0.2°, 13.604±0.2°, 14.830±0.2°, 20.645±0.2°, 23.717±0.2° and 26.262±0.2°:
12 . A method for preparing the crystal form F according to claim 11 , comprising: heating the compound as shown in the formula (I) for dissolution in an appropriate amount of a solvent VI, conducting heat filtration optionally, and conducting cooling crystallization on a resulting dissolved clarification solution to obtain the crystal form F, wherein the solvent VI is selected from dichloromethane/methyl tert-butyl ether.
13 . A crystal form I of the compound as shown in the formula (I), wherein the crystal form I has characteristic peaks in an X-ray powder diffraction pattern when a 2θ value is 7.321±0.2°, 7.538±0.2°, 12.317±0.2°, 14.643±0.2°, 15.839±0.2° and 19.458±0.2°:
14 . A method for preparing the crystal form I according to claim 13 , comprising: heating the compound as shown in the formula (I) for dissolution in an appropriate amount of a solvent VII, conducting heat filtration optionally, and conducting cooling crystallization on a resulting dissolved clarification solution, wherein the solvent VII is selected from ethyl acetate and ethanol.