IP Library › Granted Patent US 11,447,488
Granted Patent B2
US 11,447,488 · App. 16/753,630 · Granted Sep 20, 2022

Heterocyclic compounds

Inventors: Tomoaki Hasui (Kanagawa, JP); Shinji Nakamura (Kanagawa, JP); Satoshi Mikami (Kanagawa, JP); Tohru Yamashita (Kanagawa, JP)
Assignee: TAKEDA PHARMACEUTICAL COMPANY LIMITED
C07D471/04C07D407/12C07D413/10C07D413/14
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,447,488
App. No.
16/753,630
Granted
Sep 20, 2022
Kind
B2
Abstract

The present invention aims to provide a heterocyclic compound having an AMPA receptor potentiator effect, which is expected to be useful as an agent for the prophylaxis or treatment of depression, Alzheimer's disease, schizophrenia, attention deficit hyperactivity disorder (ADHD) and the like. The present invention relates to a compound represented by the formula (I): wherein each symbol is as described in the specification, or a salt thereof.

Claims (156)

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

wherein

R 1 and R 2 are each independently a hydrogen atom or a substituent, or R 1 and R 2 are bonded to each other to form, together with the adjacent nitrogen atom, a non-aromatic nitrogen-containing heterocycle that is unsubstituted or that is substituted with from one to three substituents independently selected from Substituent Group A,

R 3 is a C 1-6 alkyl group that is unsubstituted or that is substituted with from one to five substituents independently selected from Substituent Group A,

X is CR 4 or N,

R 4 , R 5 and R 6 are each independently a hydrogen atom, a halogen atom, a C 1-6 alkyl group that is unsubstituted or that is substituted with from one to five substituents independently selected from Substituent Group A or a C 1-6 alkoxy group that is unsubstituted or that is substituted with from one to five substituents independently selected from Substituent Group A, and

Ring A is a 6-membered aromatic ring optionally further substituted by 1 to 4 substituents selected from (i) a halogen atom, (ii) a C 1-6 alkyl group and (iii) a C 1-6 alkoxy group,

or a salt thereof,

wherein Substituent Group A is the group consisting of:

(1) a halogen atom,

(2) a nitro group,

(3) a cyano group,

(4) an oxo group,

(5) a hydroxy group,

(6) a C 1-6 alkoxy group,

(7) a C 6-14 aryloxy group,

(8) a C 7-16 aralkyloxy group,

(9) a 5- to 14-membered aromatic heterocyclyloxy group,

(10) a 3- to 14-membered non-aromatic heterocyclyloxy group,

(11) a C 1-6 alkyl-carbonyloxy group,

(12) a C 6-14 aryl-carbonyloxy group,

(13) a C 1-6 alkoxy-carbonyloxy group,

(14) a mono- or di-C 1-6 alkyl-carbamoyloxy group,

(15) a C 6-14 aryl-carbamoyloxy group,

(16) a 5- to 14-membered aromatic heterocyclylcarbonyloxy group,

(17) a 3- to 14-membered non-aromatic heterocyclylcarbonyloxy group,

(18) an C 1-6 alkylsulfonyloxy group,

(19) a C 6-14 arylsulfonyloxy group,

(20) an C 1-6 alkylthio group,

(21) a 5- to 14-membered aromatic heterocyclic group,

(22) a 3- to 14-membered non-aromatic heterocyclic group,

(23) a formyl group,

(24) a carboxy group,

(25) an C 1-6 alkyl-carbonyl group,

(26) a C 6-14 aryl-carbonyl group,

(27) a 5- to 14-membered aromatic heterocyclylcarbonyl group,

(28) a 3- to 14-membered non-aromatic heterocyclylcarbonyl group,

(29) a C 1-6 alkoxy-carbonyl group,

(30) a C 6-14 aryloxy-carbonyl group,

(31) a C 7-16 aralkyloxy-carbonyl group,

(32) a carbamoyl group,

(33) a thiocarbamoyl group,

(34) a mono- or di-C 1-6 alkyl-carbamoyl group,

(35) a C 6-14 aryl-carbamoyl group,

(36) a 5- to 14-membered aromatic heterocyclylcarbamoyl group,

(37) a 3- to 14-membered non-aromatic heterocyclylcarbamoyl group,

(38) a C 1-6 alkylsulfonyl group,

(39) a C 6-14 arylsulfonyl group,

(40) a 5- to 14-membered aromatic heterocyclylsulfonyl group,

(41) a C 1-6 alkylsulfinyl group,

(42) a C 6-14 arylsulfinyl group,

(43) a 5- to 14-membered aromatic heterocyclylsulfinyl group,

(44) an amino group,

(45) a mono- or di-C 1-6 alkylamino group,

(46) a mono- or di-C 6-14 arylamino group,

(47) a 5- to 14-membered aromatic heterocyclylamino group,

(48) a C 7-16 aralkylamino group,

(49) a formylamino group,

(50) a C 1-6 alkyl-carbonylamino group,

(51) a (C 1-6 alkyl)(C 1-6 alkyl-carbonyl) amino group,

(52) a C 6-14 aryl-carbonylamino group,

(53) a C 1-6 alkoxy-carbonylamino group,

(54) a C 7-16 aralkyloxy-carbonylamino group,

(55) a C 1-6 alkylsulfonylamino group,

(56) a C 6-14 arylsulfonylamino group,

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

(58) a C2-6 alkenyl group,

(59) a C 2-6 alkynyl group,

(60) a C 3-10 cycloalkyl group,

(61) a C 3-10 cycloalkenyl group, and

(62) a C 6-14 aryl group.

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

R 1 and R 2 are each independently

(1) a hydrogen atom,

(2) a C 1-6 alkyl group optionally substituted by 1 to 3 substituents selected from

(a) a cyano group, and

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

(3) a 3- to 14-membered non-aromatic heterocyclic group, or

R 1 and R 2 are bonded to each other to form, together with the adjacent nitrogen atom, a 3- to 14-membered non-aromatic nitrogen-containing heterocycle optionally further substituted by 1 to 3 substituents selected from

(a) a halogen atom,

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

(c) a C 1-6 alkoxy group;

R 3 is a C 1-6 alkyl group optionally substituted by 1 to 3 substituents selected from

(a) a halogen atom,

(b) a cyano group, and

(c) a C 1-6 alkoxy group;

X is CR 4 or N;

R 4 is

(1) a hydrogen atom,

(2) a halogen atom, or

(3) a C 1-6 alkyl group;

R 5 is

(1) a hydrogen atom, or

(2) a C 1-6 alkyl group;

R 6 is a hydrogen atom; and

Ring A is

(1) a benzene ring optionally further substituted by 1 to 4 substituents selected from (i) a halogen atom, and (ii) a C 1-6 alkoxy group, or

(2) a pyridine ring optionally further substituted by 1 to 4 halogen atoms.

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

R 1 and R 2 are each independently

(1) a hydrogen atom,

(2) a C 1-6 alkyl group optionally substituted by 1 to 3 substituents selected from

(a) a cyano group, and

(b) a C 3-6 cycloalkyl group, or

(3) a tetrahydropyranyl group, or

R 1 and R 2 are bonded to each other to form, together with the adjacent nitrogen atom,

(1) a morpholine ring optionally further substituted by 1 to 3 substituents selected from

(a) a halogen atom, and

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

(2) an oxazepane ring optionally further substituted by 1 to 3 halogen atoms,

(3) an azetidine ring optionally further substituted by 1 to 3 halogen atoms,

(4) a pyrrolidine ring optionally further substituted by 1 to 3 C 1-6 alkoxy groups,

(5) a piperidine ring optionally further substituted by 1 to 3 C 1-6 alkoxy groups, or

(6) a 5-oxa-8-azaspiro[2.6]nonane ring;

R 3 is a C 1-6 alkyl group optionally substituted by 1 to 3 substituents selected from

(a) a halogen atom,

(b) a cyano group, and

(c) a C 1-6 alkoxy group;

X is CR 4 or N;

R 4 is

(1) a hydrogen atom,

(2) a halogen atom, or

(3) a C 1-6 alkyl group;

R 5 is

(1) a hydrogen atom, or

(2) a C 1-6 alkyl group;

R 6 is a hydrogen atom; and

Ring A is

(1) a benzene ring optionally further substituted by 1 to 4 substituents selected from (i) a halogen atom, and (ii) a C 1-6 alkoxy group, or

(2) a pyridine ring optionally further substituted by 1 to 4 halogen atoms.

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

R 1 and R 2 are bonded to each other to form, together with the adjacent nitrogen atom,

(1) a morpholine ring, or

(2) an oxazepane ring optionally further substituted by 1 to 3 halogen atoms;

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

X is CH or N;

R 5 is a hydrogen atom;

R 6 is a hydrogen atom; and

Ring A is

(1) a benzene ring optionally further substituted by 1 or 2 halogen atoms, or

(2) a pyridine ring optionally further substituted by 1 or 2 halogen atoms.

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

R 1 and R 2 are bonded to each other to form, together with the adjacent nitrogen atom,

(1) a morpholine ring, or

(2) an oxazepane ring;

R 3 is a C 1-6 alkyl group substituted by two halogen atoms;

X is CH or N;

R 5 is a hydrogen atom;

R 6 is a hydrogen atom; and

Ring A is

(1) a benzene ring optionally further substituted by one halogen atom, or

(2) a pyridine ring optionally further substituted by one halogen atom.

6. (4-(1-(2,2-Difluoroethyl)-2-(trifluoromethyl)-1 H-imidazo[4,5-c]pyridin-4-yl)-2-fluorophenyl)(morpholin-4-yl)methanone, or a salt thereof.

7. (4-(1-(2,2-Difluoroethyl)-2-(trifluoromethyl)-1 H-imidazo[4,5-c]pyridin-4-yl)-2-fluorophenyl)(1,4-oxazepan-4-yl)methanone, or a salt thereof.

8. (5-(1-(2,2-Difluoroethyl)-2-(trifluoromethyl)-1 H-benzimidazol-4-yl)-3-fluoropyridin-2-yl)(morpholin-4-yl)methanone, or a salt thereof.

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

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE SECOND INVENTOR'S FIRST NAME PREVIOUSLY RECORDED ON REEL 053165 FRAME 0420. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jul 10, 2020
From: HASUI, TOMOAKI; NAKAMURA, SHINJI; MIKAMI, SATOSHI; YAMASHITA, TOHRU
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 053181/0624 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2020
From: HASUI, TOMOAKI; NAKAMURA, SHINHI; MIKAMI, SATOSHI; YAMASHITA, TOHRU
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 053165/0420 →
Priority Claims (1)
JP JP2017-195906 · Oct 6, 2017 · national
Continuity (1)
Related Publication 20200247801A1 · Aug 6, 2020