IP Library Granted Patent US 11,834,409
Granted Patent B2
US 11,834,409 · App. 18/087,233 · Granted Dec 5, 2023

Heterocyclic NMDA antagonists

Inventors: Shuhei Ikeda (Fujisawa, JP); Makoto Kamata (Fujisawa, JP); Yuya Oguro (Fujisawa, JP); Masataka Murakami (Fujisawa, JP); Minoru Nakamura (Fujisawa, JP); Fumie Yamaguchi (Fujisawa, JP); Takafumi Yukawa (Fujisawa, JP)
Assignee: Takeda Pharmaceutical Company Limited
C07D207/263A61P25/18C07D401/06
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Quick Facts
Patent No.
US 11,834,409
App. No.
18/087,233
Granted
Dec 5, 2023
Kind
B2
Abstract

A compound of formula (I), or a salt thereof that may have an antagonistic action against an NMDA receptor that includes an NR2B subunit and may be useful as a prophylactic or therapeutic agent for depression, bipolar disorder, migraine, pain, a symptom peripheral to dementia, or the like.

Claims (22)

1. A compound which is (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one or a salt thereof.

2. A compound which is crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at 8.5°±0.2°, 11.2°±0.2°, 13.5°±0.2°, 14.6°±0.2°, 14.9°±0.2°, 19.8°±0.2°, 21.5°±0.2° and 22.5°±0.2° degrees two theta.

3. A compound which is crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at at least three degrees two theta chosen from 8.5°±0.2°, 11.2°±0.2°, 13.5°±0.2°, 14.6°±0.2°, 14.9°±0.2°, 19.8°±0.2°, 21.5°±0.2° and 22.5°±0.2° degrees two theta.

4. A compound which is crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at at least four degrees two theta chosen from 8.5°±0.2°, 11.2°±0.2°, 13.5°±0.2°, 14.6°±0.2°, 14.9°±0.2°, 19.8°±0.2°, 21.5°±0.2° and 22.5°±0.2° degrees two theta.

5. A compound which is crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at 5.1°±0.2°, 10.3°±0.2°, 14.3°±0.2°, 16.5°±0.2°, 17.6°±0.2°, 22.3°±0.2° and 25.2°±0.2° degrees two theta.

6. A compound which is crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at at least three degrees two theta chosen from 5.1°±0.2°, 10.3°±0.2°, 14.3°±0.2°, 16.5°±0.2°, 17.6°±0.2°, 22.3°±0.2° and 25.2°±0.2° degrees two theta.

7. A compound which is crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at at least four degrees two theta chosen from 5.1°±0.2°, 10.3°±0.2°, 14.3°±0.2°, 16.5°±0.2°, 17.6°±0.2°, 22.3°±0.2° and 25.2°±0.2° degrees two theta.

8. A pharmaceutical composition comprising (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one or a salt thereof, and a pharmaceutically acceptable carrier.

9. The pharmaceutical composition according to claim 8 , the pharmaceutical composition comprising crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one characterized by a powder X-ray diffraction pattern comprising peaks at 8.5°±0.2°, 11.2°±0.2°, 13.5°±0.2°, 14.6°±0.2°, 14.9°±0.2°, 19.8°±0.2°, 21.5°±0.2° and 22.5°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

10. The pharmaceutical composition according to claim 8 , the pharmaceutical composition comprising crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at at least three degrees two theta chosen from 8.5°±0.2°, 11.2°±0.2°, 13.5°±0.2°, 14.6°±0.2°, 14.9°±0.2°, 19.8°±0.2°, 21.5°±0.2° and 22.5°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

11. The pharmaceutical composition according to claim 8 , the pharmaceutical composition comprising crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at at least four degrees two theta chosen from 8.5°±0.2°, 11.2°±0.2°, 13.5°±0.2°, 14.6°±0.2°, 14.9°±0.2°, 19.8°±0.2°, 21.5°±0.2° and 22.5°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

12. The pharmaceutical composition according to claim 8 , the pharmaceutical composition comprising crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at 5.1°±0.2°, 10.3°±0.2°, 14.3°±0.2°, 16.5°±0.2°, 17.6°±0.2°, 22.3°±0.2° and 25.2°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

13. The pharmaceutical composition according to claim 8 , the pharmaceutical composition comprising crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at at least three degrees two theta chosen from 5.1°±0.2°, 10.3°±0.2°, 14.3°±0.2°, 16.5°±0.2°, 17.6°±0.2°, 22.3°±0.2° and 25.2°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

14. The pharmaceutical composition according to claim 8 , the pharmaceutical composition comprising crystalline (4S,5S)-1-({6-[4-(difluoromethyl)-2-fluorophenoxy]pyridin-3-yl}methyl)-4-hydroxy-5-methylpyrrolidine-2-one, characterized by a powder X-ray diffraction pattern comprising peaks at at least four degrees two theta chosen from 5.1°±0.2°, 10.3°±0.2°, 14.3°±0.2°, 16.5°±0.2°, 17.6°±0.2°, 22.3°±0.2° and 25.2°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

15. A compound which is (5S)-1-{[2-(2,4-difluorophenoxy)pyrimidin-5-yl]methyl}-5-methylpyrrolidine-2-one or a salt thereof.

16. A compound which is crystalline (5S)-1-{[2-(2,4-difluorophenoxy)pyrimidin-5-yl]methyl}-5-methylpyrrolidine-2-one characterized by a powder X-ray diffraction pattern comprising peaks at 7.4°±0.2°, 10.3°±0.2°, 10.5°±0.2°, 14.5°±0.2°, 16.4°±0.2°, 17.8°±0.2°, 18.6°±0.2°, 19.5°±0.2°, 20.6°±0.2° and 21.3°±0.2° degrees two theta.

17. A compound which is crystalline (5S)-1-{[2-(2,4-difluorophenoxy)pyrimidin-5-yl]methyl}-5-methylpyrrolidine-2-one characterized by a powder X-ray diffraction pattern comprising peaks at at least three degrees two theta chosen from 7.4°±0.2°, 10.3°±0.2°, 10.5°±0.2°, 14.5°±0.2°, 16.4°±0.2°, 17.8°±0.2°, 18.6°±0.2°, 19.5°±0.2°, 20.6°±0.2° and 21.3°±0.2° degrees two theta.

18. A compound which is crystalline (5S)-1-{[2-(2,4-difluorophenoxy)pyrimidin-5-yl]methyl}-5-methylpyrrolidine-2-one characterized by a powder X-ray diffraction pattern comprising peaks at at least four degrees two theta chosen from 7.4°±0.2°, 10.3°±0.2°, 10.5°±0.2°, 14.5°±0.2°, 16.4°±0.2°, 17.8°±0.2°, 18.6°±0.2°, 19.5°±0.2°, 20.6θ+0.2θ and 21.3°±0.2θ degrees two theta.

19. A pharmaceutical composition comprising (5S)-1-{[2-(2,4-difluorophenoxy)pyrimidin-5-yl]methyl}-5-methylpyrrolidine-2-one or a salt thereof and a pharmaceutically acceptable carrier.

20. The pharmaceutical composition according to claim 19 , the pharmaceutical composition comprising crystalline (5S)-1-{[2-(2,4-difluorophenoxy)pyrimidin-5-yl]methyl}-5-methylpyrrolidine-2-one characterized by a powder X-ray diffraction pattern comprising peaks at 7.4°±0.20, 10.3°±0.2°, 10.5°±0.20, 14.5°±0.20, 16.4°±0.20, 17.8°±0.20, 18.6°±0.20, 19.5°±0.20, 20.6°±0.2° and 21.3°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

21. The pharmaceutical composition according to claim 19 , the pharmaceutical composition comprising crystalline (5S)-1-{[2-(2,4-difluorophenoxy)pyrimidin-5-yl]methyl}-5-methylpyrrolidine-2-one characterized by a powder X-ray diffraction pattern comprising peaks at at least three degrees two thetas of 7.4°±0.2°, 10.3°±0.2°, 10.5°±0.2°, 14.5°±0.2°, 16.4°±0.2°, 17.8°±0.2°, 18.6°±0.2°, 19.5°±0.2°, 20.6°±0.2° and 21.3°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

22. The pharmaceutical composition according to claim 19 , the pharmaceutical composition comprising crystalline (5S)-1-{[2-(2,4-difluorophenoxy)pyrimidin-5-yl]methyl}-5-methylpyrrolidine-2-one characterized by a powder X-ray diffraction pattern comprising peaks at at least four degrees two thetas of 7.4°±0.2°, 10.3°±0.2°, 10.5°±0.2°, 14.5°±0.2°, 16.4°±0.2°, 17.8°±0.2°, 18.6°±0.2°, 19.5°±0.2°, 20.6°±0.2° and 21.3°±0.2° degrees two theta, and a pharmaceutically acceptable carrier.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2023
From: IKEDA, SHUHEI; KAMATA, MAKOTO; OGURO, YUYA; AIDA, JUMPEI; TAWARAISHI, TAISUKE; WAKABAYASHI, TAKESHI; OYABU, NORIO; OCHIDA, ATSUKO; IWANAGA, KOUICHI; YAMAMOTO, SATOSHI; MURAKAMI, MASATAKA; NAKAMURA, MINORU; YAMAGUCHI, FUMIE; YUKAWA, TAKAFUMI
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 065263/0402 →
Priority Claims (1)
JP 2019-206311 · Nov 14, 2019 · national
Continuity (2)
Continuation 17755907
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