Crystalline form of ATR inhibitor and use thereof
Crystalline forms of an ATR inhibitor, preparation methods therefor, and the use thereof in the preparation of a drug for treating ATR-related diseases. In particular, crystalline forms of an ATR inhibitor represented by formula (I), physicochemical and biochemical properties of the same, preparation methods for, and uses of the same, in the preparation of a drug for treating ATR-related diseases.
1 . A crystal form of a compound of formula (I):
which is selected from the group consisting of:
(1) Crystal Form A, wherein,
the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 20 angles: 8.10±0.20°, 18.33±0.20° and 22.63±0.20°;
(2) Crystal Form B, wherein,
the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 20 angles: 8.45±0.20°, 10.87±0.20° and 20.56±0.20°.
2 . The crystal form according to claim 1 , which is
the Crystal Form A having an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 20 angles: 7.46±0.20°, 8.10±0.20°, 13.03±0.20°, 15.07±0.20°, 15.58±0.20°, 16.19±0.20°, 18.33±0.20° and 22.63±0.20°.
3 . The crystal form according to claim 2 , wherein,
the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 20 angles: 7.46±0.20°, 8.10±0.20°, 13.03±0.20°, 13.46±0.20°, 15.07±0.20°, 15.58±0.20°, 16.19±0.20°, 18.33±0.20°, 21.17±0.20° and 22.63±0.20°.
4 . The crystal form according to claim 3 , wherein,
the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 20 angles: 7.46°, 8.10°, 11.24°, 13.03°, 13.46°, 15.07°, 15.58°, 15.98°, 16.19°, 17.70°, 18.33°, 19.60°, 21.17°, 22.63°, 23.84°, 25.56° and 26.57°.
5 . The crystal form according to claim 4 , wherein,
the Crystal Form A has an XRPD pattern as shown in FIG. 1 .
6 . The crystal form according to claim 1 , which is
the Crystal Form B having an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 20 angles: 8.45±0.20°, 10.87±0.20°, 14.83±0.20°, 15.54±0.20°, 17.33±0.20°, 20.56±0.20°, 22.00±0.20° and 22.63±0.20°.
7 . The crystal form according to claim 6 , wherein,
the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 20 angles: 8.45±0.20°, 10.87±0.20°, 14.83±0.20°, 15.54±0.20°, 17.33±0.20°, 20.08±0.20°, 20.56±0.20°, 22.00±0.20°, 22.63±0.20° and 25.26±0.20°.
8 . The crystal form according to claim 7 , wherein,
the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 20 angles: 8.45°, 9.20°, 10.87°, 12.57°, 14.14°, 14.53°, 14.83°, 15.54°, 16.80°, 17.33°, 18.43°, 19.84°, 20.08°, 20.56°, 21.39°, 22.00°, 22.44°, 22.63°, 23.26°, 25.26°, 25.85° and 26.98°.
9 . The crystal form according to claim 8 , wherein,
the Crystal Form B has an XRPD pattern as shown in FIG. 2 .
10 . The crystal form according to claim 1 , which is
the Crystal Form B having a Differential Scanning Calorimetry curve (DSC) having one onset point of endothermic peak at 174.3±3° C.
11 . The crystal form according to claim 10 , wherein,
the Crystal Form B has a DSC pattern as shown in FIG. 3 .
12 . The crystal form according to claim 1 , which is
the Crystal Form B having a Thermogravimetric Analysis curve (TGA), wherein the weight loss at 150°±3° C. is 1.49%.
13 . The crystal form according to claim 12 , wherein,
the Crystal Form B has a TGA pattern as shown in FIG. 4 .
14 . A process for preparing the Crystal Form A of the compound of formula (I) as defined in claim 1 , comprising:
1) adding the compound of formula (I) into ethanol solvent;
2) adding water;
3) stirring for 100-120 h;
4) performing recrystallization at room temperature to obtain the Crystal Form A.
15 . A process for preparing the Crystal Form B of the compound of formula (I) as defined in claim 1 , comprising:
1) adding the compound of formula (I) into a solvent;
2) heating to a temperature with stirring for 2.5-120 h;
3) performing recrystallization at room temperature to obtain the Crystal Form B.
16 . The process according to claim 15 , wherein
the solvent is methanol, methyl tertiary butyl ether, methanol/water (VN, 1:0.3-1), acetone/water (V/V, 1:1), isopropanol/water (V/V, 1:1), ethyl acetate/n-heptane (V/V, 1:1), isopropyl acetate/n-heptane (V/V, 1:1), ethanol/n-heptane (V/V, 1:1), acetonitrile/n-heptane (V/V, 1:1), isopropanol/n-heptane (V/V, 1:1) or dichloromethane/n-heptane (V/V, 1:1).
17 . The process according to claim 16 , wherein
the temperature is 25-70° C.
18 . The process according to claim 15 , wherein
the concentration range of the compound of formula (I) is selected from the group consisting of 25 mg/mL-50 mg/mL.
19 . A method for treating colorectal cancer, comprising administering the crystal form according to claim 1 to a subject in need thereof.
20 . A pharmaceutical composition, comprising the crystal form according to claim 1 .