IP Library Granted Patent US 10,752,601
Granted Patent B2
US 10,752,601 · App. 16/482,149 · Granted Aug 25, 2020

Crystal form and salt of 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole

Inventors: Junichiro Uda (Saitama, JP); Seiichi Kobashi (Saitama, JP); Misa Hasegawa (Saitama, JP)
Assignee: Fuji Yakuhin Co., Ltd
C07D277/62C07B2200/13
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Quick Facts
Patent No.
US 10,752,601
App. No.
16/482,149
Granted
Aug 25, 2020
Kind
B2
Abstract

A type II crystal of 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole, having characteristic peaks at least around 15.1, 18.1, 22.8, 23.7, and 24.0 degrees in a diffraction angle (2θ) by X-ray powder diffraction, and method for producing said type II crystal.

Claims (14)

1. A type II crystal of 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole, having characteristic peaks at least around 15.1, 18.1, 22.8, 23.7, and 24.0 degrees in a diffraction angle (20) by X-ray powder diffraction.

2. The type II crystal according to claim 1 , characterized by having a heat absorption peak around 212° C. in DSC analysis.

3. A pharmaceutical composition containing a crystal according to claim 1 and a pharmaceutically acceptable carrier.

4. A method for producing a type II crystal of 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole, comprising:

crystallization of a compound from an organic solvent to form the type II crystal of 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole.

5. The method according to claim 4 , wherein the organic solvent for crystallization comprises a mixture of a dissolving solvent and a poor solvent.

6. The method according to claim 5 , wherein the poor solvent comprises one of 2-propanol, ethanol, n-hexane, cyclohexane, cumene, paraxylene, methylcyclohexane, 2,2,4-trimethylpentane, toluene, n-pentane, n-heptane, and acetonitrile.

7. The method according to claim 5 , wherein the dissolving solvent comprises one of tetrahydrofuran, ethyl acetate, and dimethylsulfoxide.

8. The method according to claim 4 , further comprising:

dissolving the 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole compound in the organic solvent by heating.

9. The method according to claim 8 , further comprising:

after the step of dissolving the 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole compound in the organic solvent by heating, cooling the dissolved 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole compound.

10. The method according to claim 4 , wherein the type II crystal of 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole is characterized by peaks at least around 15.1, 18.1, 22.8, 23.7, and 24.0 degrees in a diffraction angle (20) by X-ray powder diffraction.

11. The method according to claim 10 , wherein the type II crystal of 3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole is characterized by a heat absorption peak around 212° C. in DSC analysis.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2019
From: UDA, JUNICHIRO; KOBASHI, SEIICHI; HASEGAWA, MISA
To: FUJI YAKUHIN CO., LTD.
Reel/Frame 050136/0922 →
Priority Claims (1)
JP 2017-099334 · Apr 28, 2017 · national
Continuity (1)
Related Publication 20190389818A1 · Dec 26, 2019