IP Library Granted Patent US 10,016,433
Granted Patent B2
US 10,016,433 · App. 15/647,911 · Granted Jul 10, 2018

Salt of fused heterocyclic derivative and crystal thereof

Inventors: Kazumichi Jo (Joetsu, JP); Hideki Takeuchi (Joetsu, JP)
Assignee: KISSEI PHARMACEUTICAL CO., LTD.
A61K31/519A61K9/0053A61K31/14C07D495/04C07B2200/13
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Quick Facts
Patent No.
US 10,016,433
App. No.
15/647,911
Granted
Jul 10, 2018
Kind
B2
Abstract

The present invention provides 3-[2-fluoro-5-(2,3-difluoro-6-methoxybenzyl-oxy)-4-methoxyphenyl]-2,4-dioxo-1,2,3,4-tetrahydrothieno[3,4-d]pyrimidine-5-carboxylic acid choline salt having excellent solubility and storage stability.

Claims (15)

1. A method of treating precocious puberty in a subject, said method comprising administering to said subject a therapeutically effective amount of a compound represented by the formula:

2. The method of claim 1 , wherein said compound is administered orally.

3. The method of claim 1 , wherein said subject is a human.

4. The method of claim 1 , wherein said compound is crystalline.

5. The method of claim 4 , wherein said compound exhibits characteristic peaks at diffraction angles (2θ(°)) of 7.1, 11.5, 19.4, 20.3, 21.5, 22.0, 22.6, 23.5, and 26.2 in a powder X-ray diffraction diagram.

6. The method of claim 4 , wherein said compound is characterized by an X-ray powder diffraction spectrum substantially as depicted in FIG. 1 .

7. The method of claim 4 , wherein said compound exhibits characteristic peaks at chemical shift values (δ(ppm)) of 155.8, 149.8, 145.3, 118.0, 113.7, 111.6, 110.3, 98.1, 69.8, 58.7, 57.1, and 55.5 in a 13 C solid-state nuclear magnetic resonance (NMR) spectrum.

8. The method of claim 4 , wherein said compound is characterized by a 13 C solid-state NMR spectrum substantially as depicted in FIG. 3 .

9. The method of claim 4 , wherein said compound exhibits characteristic peaks at chemical shift values (δ(ppm)) of −131.6, −145.2, and −151.8 in a 19 F solid-state NMR spectrum.

10. The method of claim 4 , wherein said compound is characterized by a 19 F solid-state NMR spectrum substantially as depicted in FIG. 5 .

11. The method of claim 4 , wherein said compound exhibits an endotherm at about 213° C. as measured by differential thermal analysis.

12. The method of claim 4 , wherein said compound is characterized by a differential thermal analysis curve substantially as depicted in FIG. 2 .

13. The method of claim 4 , wherein said compound is characterized by a thermogravimetric analysis curve substantially as depicted in FIG. 2 .

14. The method of claim 1 , said method comprising administering to said subject a pharmaceutical composition comprising said therapeutically effective amount of said compound.

15. The method of claim 14 , wherein said pharmaceutical composition is a tablet or capsule.

Priority Claims (1)
JP 2010-027806 · Feb 10, 2010 · national
Continuity (3)
Continuation 14867501 · Sep 28, 2015
Division 13577832
Related Publication 20170319588A1 · Nov 9, 2017
Cited By (1)
US 12,280,052