IP Library › Granted Patent US 10,807,987
Granted Patent B2
US 10,807,987 · App. 16/366,710 · Granted Oct 20, 2020

Heterocyclic compound and use thereof

Inventors: Yuya Oguro (Fujisawa, JP); Shigemitsu Matsumoto (Fujisawa, JP); Takeshi Wakabayashi (Fujisawa, JP); Norihito Tokunaga (Fujisawa, JP); Taku Kamei (Fujisawa, JP); Mitsuhiro Ito (Fujisawa, JP); Satoshi Mikami (Fujisawa, JP); Masaki Seto (Fujisawa, JP); Shinji Morimoto (Fujisawa, JP); Shinji Nakamura (Fujisawa, JP); Sachie Takashima (Fujisawa, JP); Masataka Murakami (Fujisawa, JP); Masaki Daini (Fujisawa, JP); Makoto Kamata (Fujisawa, JP); Minoru Nakamura (Fujisawa, JP); Yasufumi Wada (Fujisawa, JP); Hiroyuki Kakei (Fujisawa, JP); Kazuaki Takami (Fujisawa, JP); Taisuke Tawaraishi (Fujisawa, JP); Jumpei Aida (Fujisawa, JP); Kouichi Iwanaga (Fujisawa, JP); Satoshi Yamamoto (Fujisawa, JP)
Assignee: Takeda Pharmaceutical Company Limited
C07D487/04A61K9/2095A61K9/4833A61P25/00C07D471/04
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Quick Facts
Patent No.
US 10,807,987
App. No.
16/366,710
Granted
Oct 20, 2020
Kind
B2
Abstract

The present invention provides a heterocyclic compound having an antagonistic action on an NMDA receptor containing the NR2B subunit, and expected to be useful as an agent for the prophylaxis or treatment of major depression, bipolar disorder, migraine, pain, behavioral and psychological symptoms of dementia and the like. The present invention relates to a compound represented by the formula (I): wherein each symbol is as described in the description, or a salt thereof.

Claims (90)

1. A compound represented by the formula (I):

wherein

the group represented by

is a group represented by

X a1 is CH or a nitrogen atom;

X a2 is

(1) CR a wherein R a is

(a) a hydrogen atom,

(b) a halogen atom, or

(c) a C 1-6 alkyl group, or

(2) a nitrogen atom;

X a3 is

(1) CR a wherein R a is

(a) a hydrogen atom, or

(b) a C 1-6 alkyl group, or

(2) a nitrogen atom;

X a4 is

(1) CR a wherein R a is

(a) a hydrogen atom, or

(b) a C1-6 alkyl group, or

(2) a nitrogen atom; and

X a5 is

(1) CR a wherein R a is

(a) a hydrogen atom,

(b) a C 1-6 alkyl group optionally substituted by 1 to 3 substituents selected from a halogen atom and a C 1-6 alkoxy group,

(c) a C 1-6 alkoxy group, or

(d) a C 3-10 cycloalkyl group, or

(2) a nitrogen atom;

provided that when X a5 is CR a , then at least one of X a1 , X a2 and X a3 is a nitrogen atom;

X b1 is CH or a nitrogen atom;

X b2 is CR b wherein R b is

(a) a hydrogen atom, or

(b) a C 1-6 alkyl group;

X b3 is a nitrogen atom optionally substituted by a C 1-6 alkyl group optionally substituted by 1 to 3 halogen atoms; and

X b4 is CR b wherein R b is

(a) a hydrogen atom, or

(b) a C 1-6 alkyl group;

R 1 and R 2 are each a hydrogen atom; and

R 3 is a group represented by

R 4 is

(1) a C 1-6 alkyl group optionally substituted by 1 to 3 halogen atoms,

(2) a C 1-6 alkoxy group optionally substituted by 1 to 3 halogen atoms,

(3) a C 3-10 cycloalkyloxy group, or

(4) a halogen atom;

Y is a nitrogen atom or CR 6 wherein R 6 is a hydrogen atom or a halogen atom; and

Ring C 1 is a benzene ring (i.e., Y is CR 6 ) or a pyridine ring (i.e., Y is N), each of which is optionally further substituted by one halogen atom;

R 5 is a C 1-6 alkyl group optionally substituted by 1 to 3 halogen atoms; and

Ring C 2 is a thiophene ring substituted by only R 5 ,

or a salt thereof.

2. The compound or salt according to claim 1 , wherein

the group represented by

is a group represented by

X a1 is CH or a nitrogen atom;

X a2 is CH;

X a3 is CH or a nitrogen atom;

X a4 is CH; and

X a5 is CH or a nitrogen atom;

provided that when X a5 is CH, then at least one of X a1 and X a3 is a nitrogen atom;

X b1 is CH;

X b2 is CH;

X b3 is a nitrogen atom optionally substituted by a C 1-6 alkyl group; and

X b4 is CH;

R 1 and R 2 are both hydrogen atoms; and

R 3 is a group represented by

R 4 is a C 1-6 alkoxy group optionally substituted by 1 to 3 halogen atoms;

Y is a nitrogen atom or CH; and

Ring C 1 is a benzene ring (i.e., Y is CH) or a pyridine ring (i.e., Y is N), each of which is optionally further substituted by one halogen atom.

3. The compound or salt according to claim 1 , wherein

the group represented by

is a group represented by

X a1 is CH or a nitrogen atom;

X a2 is CH;

X a3 is CH;

X a4 is CH; and

X a5 is CH or a nitrogen atom;

provided that when X a5 is CH, then X a1 is a nitrogen atom;

X b1 is CH;

X b2 is CH;

X b3 is a nitrogen atom optionally substituted by a C 1-6 alkyl group; and

X b4 is CH;

R 1 and R 2 are both hydrogen atoms; and

R 3 is a group represented by

R 4 is a C 1-6 alkoxy group optionally substituted by 1 to 3 halogen atoms;

Y is a nitrogen atom or CH; and

Ring C 1 is a benzene ring (i.e., Y is CH) or a pyridine ring (i.e., Y is N), each of which is optionally further substituted by one halogen atom.

4. 6-(Difluoromethoxy)-5-fluoro-N-[(pyrazolo[1,5-b]pyridazin-3-yl)methyl]pyridine-3-carboxamide or a salt thereof.

5. 3-Fluoro-N-[([1,2,3]triazolo[1,5-a]pyridin-3-yl)methyl]-4-(trifluoromethoxy)benzamide or a salt thereof.

6. 6-(Difluoromethoxy)-5-fluoro-N-[(1-methyl-1H-imidazo[1,2-b]pyrazol-7-yl)methyl]pyridine-3-carboxamide or a salt thereof.

7. A pharmaceutical composition comprising the compound or salt according to claim 1 , and a pharmacologically acceptable carrier.

8. A method for the treatment of major depression, bipolar disorder, migraine, pain, or behavioral and psychological symptoms of dementia in a mammal, which comprises administering an effective amount of the compound or salt according to claim 1 to the mammal.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2019
From: OGURO, YUYA; MATSUMOTO, SHIGEMITSU; WAKABAYASHI, TAKESHI; TOKUNAGA, NORIHITO; KAMEI, TAKU; ITO, MITSUHIRO; MIKAMI, SATOSHI; SETO, MASAKI; MORIMOTO, SHINJI; NAKAMURA, SHINJI; TAKASHIMA, SACHIE; MURAKAMI, MASATAKA; DAINI, MASAKI; KAMATA, MAKOTO; NAKAMURA, MINORU; WADA, YASUFUMI; KAKEI, HIROYUKI; TAKAMI, KAZUAKI; TAWARAISHI, TAISUKE; AIDA, JUMPEI; IWANAGA, KOUICHI; YAMAMOTO, SATOSHI
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 049558/0407 →
Priority Claims (1)
JP 2018-062939 · Mar 28, 2018 · national
Continuity (1)
Related Publication 20190300536A1 · Oct 3, 2019
Cited By (2)
US 12,630,509 US 12,637,418