Crystals of quinazoline derivative and preparation method therefor
The invention relates to Crystal form I, Crystal form II and Crystal form III of N-(4-((3-chloro-4-fluorophenyl)amino)-7-((7-methyl-7-azaspiro[3.5]nonan-2-yl)methoxy)quinazolin-6-yl)acrylamide represented by the following Formula (I), and preparation methods thereof, wherein the Crystal form I has an X-ray powder diffraction pattern having characteristic peaks at the 2θ positions of 6.7±0.2°, 7.9±0.2°, 8.6±0.2°, 12.0±0.2°, 13.9±0.2°, 15.9±0.2°, 17.3±0.2°, 18.3±0.2°, 18.7±0.2°, 21.0±0.2°, and 23.0±0.2°, as determined by using Cu-Kα radiation; the Crystal form II has an X-ray powder diffraction pattern having characteristic peaks at the 2θ positions of 6.9±0.2°, 8.5±0.2°, 14.8±0.2°, 15.6±0.2°, 16.7±0.2°, 17.1±0.2°, 17.9±0.2°, 18.7±0.2°, 19.1±0.2°, 21.5±0.2°, 23.5±0.2°, and 25.7±0.2°, as determined by using Cu-Kα radiation; and the Crystal form III has an X-ray powder diffraction pattern having characteristic peaks at the 2θ positions of 4.9±0.2°, 6.1±0.2°, 7.4±0.2°, 11.4±0.2°, 12.2±0.2°, 16.6±0.2°, and 18.4±0.2°, as determined by using Cu-Kα radiation.
1. Crystal form I of N-(4-((3-chloro-4-fluorophenyl)amino)-7-((7-methyl-7-azaspiro[3.5]nonan-2-yl)methoxy)quinazolin-6-yl)acrylamide represented by Formula (I), wherein the Crystal form I exhibits an X-ray powder diffraction pattern having characteristic peaks at the 2θ positions of 6.7±0.2°, 7.9±0.2°, 8.6±0.2°, 12.0±0.2°, 13.9±0.2°, 15.9±0.2°, 17.3±0.2°, 18.3±0.2°, 18.7±0.2°, 21.0±0.2°, and 23.0±0.2°, as determined by using Cu-Kα radiation,
2. The Crystal form I according to claim 1 , wherein the X-ray powder diffraction pattern further has characteristic peaks at the 2θ positions of 16.2±0.2°, 23.0±0.2°, 23.4±0.2°, 25.3±0.2°, 26.0±0.2°, 26.5±0.2°, 27.7±0.2°, and 28.0±0.2°, as determined by using Cu-Kα radiation.
3. The Crystal form I according to claim 2 , wherein the X-ray powder diffraction pattern further has characteristic peaks at the 2θ positions of 13.6±0.2°, 21.5±0.2°, 21.9±0.2°, and 32.2±0.2°, as determined by using Cu-Kα radiation.
4. The Crystal form I according to claim 1 , which exhibits a DSC thermogram having an endothermic conversion peak at 75-150° C., and a maximum endothermic conversion temperature of 113-114° C.
5. The Crystal form I according to claim 1 , which is a hydrate having a water content of 2.5%-4%.
6. The Crystal form I according to claim 1 , which is a monohydrate.
7. A method for preparing the Crystal form I according to claim 1 , comprising the following steps: N-(4-((3-chloro-4-fluorophenyl)amino)-7-((7-methyl-7-azaspiro[3.5]nonan-2-yl)methoxy)quinazolin-6-yl)acrylamide is dissolved in a lower nitrile organic solvent or in a mixed solvent of a lower ester organic solvent and a lower alcohol organic solvent, and then subjected to addition of a poor solvent or recrystallization to produce a crystal, and then the crystal is subjected to filtration and drying to obtain Crystal form I.
8. The method according to claim 7 , wherein the lower nitrile organic solvent is acetonitrile; the lower ester organic solvent is ethyl acetate or ethyl formate; the lower alcohol organic solvent is selected from the group consisting of methanol, ethanol and isopropanol; and the poor solvent is selected from water and/or n-heptane.
9. Crystal form II of quinazoline derivative N-(4-((3-chloro-4-fluorophenyl)amino)-7-((7-methyl-7-azaspiro[3.5]nonan-2-yl)methoxy)quinazolin-6-yl)acrylamide represented by Formula (I), wherein the Crystal form II exhibits a X-ray powder diffraction pattern having characteristic peaks at the 2θ positions of 6.9±0.2°, 8.5±0.2°, 11.6±0.2°, 14.0±0.2°, 14.8±0.2°, 15.6±0.2°, 16.0±0.2°, 16.7±0.2°, 17.1±0.2°, 17.3±0.2°, 17.9±0.2°, 18.7±0.2°, 19.1±0.2°, 19.7±0.2°, 20.6±0.2°, 21.5±0.2°, 22.1±0.2°, 22.4±0.2°, 23.5±0.2°, 24.5±0.2°, 25.7±0.2°, 26.1±0.2°, 28.3±0.2°, 28.6±0.2°, 31.7±0.2° and 34.6±0.2°, as determined by using Cu-Kα radiation,
10. The Crystal form II according to claim 9 , which exhibits a DSC thermogram having an endothermic conversion peak at 75-169° C., and a maximum endothermic conversion temperature of 123-124° C.
11. The Crystal form II according to claim 9 , which is a hydrate having a water content of 3%-4%.
12. The Crystal form II according to claim 9 , which is a monohydrate.
13. A method for preparing the Crystal form II according to claim 9 , comprising the following steps: N-(4-((3-chloro-4-fluorophenyl)amino)-7-((7-methyl-7-azaspiro[3.5]nonan-2-yl)methoxy)quinazolin-6-yl)acrylamide is dissolved in a lower ester organic solvent, an aromatic hydrocarbon organic solvent, or a mixed solvent of a lower ester organic solvent and a lower alcohol organic solvent, and then subjected to addition of a poor solvent or recrystallization to produce a crystal, and then the crystal is subjected to filtration and drying to obtain Crystal form II;
wherein the lower ester organic solvent is selected from the group consisting of ethyl acetate, ethyl formate, methyl acetate and isopropyl acetate; the aromatic hydrocarbon organic solvent is toluene; the lower alcohol organic solvent is selected from the group consisting of methanol, ethanol and isopropanol; and the poor solvent is water.
14. Crystal form III of N-(4-((3-chloro-4-fluorophenyl)amino)-74(7-methyl-7-azaspiro[3.5]nonan-2-yl)methoxy)quinazolin-6-yl)acrylamide represented by Formula (I), wherein the Crystal form III exhibits an X-ray powder diffraction pattern having characteristic peaks at the 2θ positions of 4.9±0.2°, 6.1±0.2°, 7.4±0.2°, 9.2±0.2°, 11.2±0.2°, 11.4±0.2°, 12.2±0.2°, 13.4±0.2°, 14.8±0.2°, 16.6±0.2°, 18.4±0.2°, 19.2±0.2°, 20.4±0.2°, 20.8±0.2°, 22.4±0.2°, 23.2±0.2°, 23.8±0.2°, 25.7±0.2°, 27.5±0.2° and 30.1±0.2°, as determined by using Cu-Kα radiation,
15. The Crystal form III according to claim 14 , which exhibits a DSC thermogram having an endothermic conversion peak at 50-125° C., and a maximum endothermic conversion temperature of 96-97° C.
16. The Crystal form III according to claim 14 , which is a hydrate having a water content of 2.5%-4%.
17. The Crystal form III according to claim 14 , which is a monohydrate.
18. A method for preparing the Crystal form III according to claim 14 , comprising the following steps: N-(4-(3-chloro-4-fluorophenyl)amino)-7-((7-methyl-7-azaspiro[3.5]nonan-2-yl)methoxy)quinazolin-6-yl)acrylamide is subjected to recrystallization using a lower alcohol organic solvent or a lower halo hydrocarbon organic solvent to produce a solid, and then the solid is subjected to filtration and drying to obtain Crystal form III;
wherein the lower alcohol organic solvent is selected from the group consisting of methanol, ethanol and isopropanol; and the lower halo hydrocarbon organic solvent is dichloromethane.
19. A method for preparing the Crystal form III according to claim 14 , comprising the following steps: N-(4-((3-chloro-4-fluorophenyl)amino)-7-((7-methyl-7-azaspiro[3.5]nonan-2-yl)methoxy)quinazolin-6-yl)acrylamide is dissolved in a lower ketone organic solvent, and then subjected to addition of an alicyclic hydrocarbon organic solvent dropwise to produce a solid, and then the solid is subjected to filtration and drying to obtain Crystal form III;
wherein the lower ketone organic solvent is selected from the group consisting of acetone and butanone; and the alicyclic hydrocarbon organic solvent is selected from the group consisting of cyclopentane and cyclohexane.
20. A pharmaceutical formulation, comprising the Crystal form I according to claim 1 , and one or more pharmaceutically acceptable carriers and/or diluents.