IP Library › Granted Patent US 11,174,270
Granted Patent B2
US 11,174,270 · App. 16/968,206 · Granted Nov 16, 2021

Crystal form of 3,4-dihydrothieno[3,2-d]pyrimidine compound and preparation method thereof

Inventors: Jian Xiong (Shanghai, CN); Jingjing Wang (Shanghai, CN); Boyu Hu (Shanghai, CN); Haizhong Tan (Shanghai, CN); Kevin X. Chen (Shanghai, CN); Jian Li (Shanghai, CN); Shuhui Chen (Shanghai, CN)
Assignee: Phaeno Therapeutics Co., Ltd.
C07D495/04C07B2200/13
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Quick Facts
Patent No.
US 11,174,270
App. No.
16/968,206
Granted
Nov 16, 2021
Kind
B2
Abstract

A crystal form A of a 3,4-dihydrothieno[3,2-d]pyrimidine compound (1), a preparation method therefor and an application thereof in the preparation of an anti-human cytomegalovirus (HCMV) drug.

Claims (15)

1. A crystal form A of compound 1, wherein the X-ray powder diffraction pattern thereof has characteristic diffraction peaks at the following 2θ angles: 17.69±0.2°, 20.00±0.2°, and 20.63±0.2°,

2. The crystal form A of compound 1 according to claim 1 , wherein the X-ray powder diffraction pattern thereof has characteristic diffraction peaks at the following 2θ angles: 9.15±0.2°, 11.06±0.2°, 11.95±0.2°, 17.69±0.2°, 19.03±0.2°, 19.46±0.2°, 20.00±0.2°, and 20.63±0.2°.

3. The crystal form A of compound 1 according to claim 2 , wherein the XRPD pattern thereof is shown in FIG. 1 .

4. The crystal form A of compound 1 according to claim 1 wherein the differential scanning calorimetry curve thereof has a starting point of the endothermic peak at 214.47±° C.

5. The crystal form A of compound 1 according to claim 4 , wherein the DSC curve thereof is shown in FIG. 2 .

6. The crystal form A of compound 1 according to claim 1 wherein the thermogravimetric analysis curve thereof has a weight loss of 0.1206% at 120.00±2° C.

7. The crystal form A of compound 1 according to claim 6 , wherein the TGA curve thereof is shown in FIG. 3 .

8. A method of preparing the crystal form A of compound 1,

comprising adding the compound 1 to a mixed solvent of alcoholic solvent and water, heating to dissolve, and then cooling and crystallizing.

9. The method of preparing the crystal form A of compound 1 according to claim 8 , wherein the alcoholic solvent is selected from the group consisting of methanol, ethanol and isopropanol.

10. The method of preparing the crystal form A of compound 1 according to claim 8 , wherein the mixed solvent of alcoholic solvent and water is a mixed solvent of ethanol and water.

11. The method of preparing the crystal form A of compound 1 according to claim 8 , wherein in the mixed solvent of alcoholic solvent and water, the volume ratio of the alcoholic solvent to water is selected from 1:0.2 to 1:1.5.

12. A method of treating a disease related to HCMV virus in a subject in need thereof, comprising administering to the subject the crystal form A of compound 1 according to claim 1 .

13. The crystal form A of compound 1 according to claim 4 , wherein the thermogravimetric analysis curve thereof has a weight loss of 0.1206% at 120.00±2° C.

14. The crystal form A of compound 1 according to claim 7 , wherein the TGA curve thereof is shown in FIG. 3 .

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2021
From: MEDSHINE DISCOVERY INC.
To: PHAENO THERAPEUTICS CO., LTD.
Reel/Frame 057856/0299 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 13, 2021
From: MEDSHINE DISCOVERY INC.
To: PHAENO THERAPEUTICS CO., LTD.
Reel/Frame 057777/0159 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2020
From: XIONG, JIAN; WANG, JINGJING; HU, BOYU; TAN, HAIZHONG; CHEN, KEVIN X.; LI, JIAN; CHEN, SHUHUI
To: MEDSHINE DISCOVERY INC.
Reel/Frame 054544/0499 →
Priority Claims (1)
CN 201810130625.8 · Feb 8, 2018 · national
Continuity (1)
Related Publication 20210024538A1 · Jan 28, 2021