IP Library Granted Patent US 12673941
Granted Patent B2
US 12673941 · App. 19/177,218 · Granted Jul 7, 2026

Tertiary amide derivatives substituted with 4-membered ring structure

Inventors: Shunichiro Uesugi (Osaka, JP); Yusuke Kamei (Osaka, JP); Hitoshi Ban (Osaka, JP); Seiji Kamioka (Osaka, JP); Yusuke Imazaki (Osaka, JP); Hideaki Ogiwara (Tokyo, JP); Mariko Sasaki (Tokyo, JP)
Assignees: Sumitomo Pharma Co., Ltd.; NATIONAL CANCER CENTER
C07D405/14A61K31/4184A61K31/4439A61K31/4545A61K31/4985A61K45/06A61P35/00C07D401/14C07D403/14C07D487/04
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 12673941
App. No.
19/177,218
Granted
Jul 7, 2026
Kind
B2
Abstract

[Problem] The present disclosure provides tertiary amide derivatives substituted with a 4-membered ring structure that are useful as medicines and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising the same, and therapeutic agents and/or prophylactic agents for conditions in which CBP/P300 is involved, comprising the composition. [Solving Means] More specifically, the present disclosure provides a compound represented by the following Formula (1): wherein A represents CHF, or CH 2 , B represents the following Formula (B-1): Ring Q represents an optionally substituted 6- to 10-membered aromatic hydrocarbon ring, or an optionally substituted 5- to 10-membered aromatic heterocycle, Z represents —O—, —N(R 7a )—, an optionally substituted 6- to 10-membered divalent aromatic ring group, an optionally substituted 5- to 10-membered divalent aromatic heterocyclic group, an optionally substituted 4- to 10-membered divalent non-aryl heterocyclic group, and R 1 , R 2a , R 2b , R 3 , R 4 , and R 5 are as described in the specification, or a pharmaceutically acceptable salt thereof.

Claims (14)

1 . A compound or a pharmaceutically acceptable salt thereof, wherein the compound is

2-[(1′S,3′R)-3′-fluoro-5′-{1-[1-(oxetan-3-yl)azetidin-3-yl]-1H-pyrazol-4-yl}-2,5-dioxo-2′,3′-dihydrospiro[imidazolidine-4,1′-inden]-1-yl]-N-[(5-fluoropyridin-2-yl)methyl]-N-[3-(trifluoromethyl)oxetan-3-yl]acetamide.

2 . A compound or a pharmaceutically acceptable salt thereof, wherein the compound is

2-[(1′S,3′R)-3′-fluoro-5′-(1-methyl-1H-pyrazol-4-yl)-2,5-dioxo-2′,3′-dihydrospiro[imidazolidine-4,1′-inden]-1-yl]-N-[(4-fluorophenyl)methyl]-N-[1-methyl-3-(trifluoromethyl)azetidin-3-yl]acetamide.

3 . A compound or a pharmaceutically acceptable salt thereof, wherein the compound is

2-[(1′S,3′R)-3′-fluoro-5′-(1-methyl-1H-pyrazol-4-yl)-2,5-dioxo-2′,3′-dihydrospiro[imidazolidine-4,1′-inden]-1-yl]-N-[(5-fluoropyridin-2-yl)methyl]-N-[1-methyl-3-(trifluoromethyl)azetidin-3-yl]acetamide.

4 . A compound or a pharmaceutically acceptable salt thereof, wherein the compound is

2-{(1′S,3′R)-3′-fluoro-5′-[1-(oxetan-3-yl)-1H-pyrazol-4-yl]-2,5-dioxo-2′,3′-dihydrospiro[imidazolidine-4,1′-inden]-1-yl}-N-[(5-fluoropyridin-2-yl)methyl]-N-[1-methyl-3-(trifluoromethyl)azetidin-3-yl]acetamide.

5 . A compound or a pharmaceutically acceptable salt thereof, wherein the compound is

2-[(1′S,3′R)-3′-fluoro-5′-{1-[(oxetan-3-yl)methyl]-1H-pyrazol-4-yl}-2,5-dioxo-2′,3′-dihydrospiro[imidazolidine-4,1′-inden]-1-yl]-N-[(5-fluoropyridin-2-yl)methyl]-N-[1-methyl-3-(trifluoromethyl)azetidin-3-yl]acetamide.

6 . A compound or a pharmaceutically acceptable salt thereof, wherein the compound is

2-[(1′S,3′R)-5′-(1-ethyl-1H-pyrazol-4-yl)-3′-fluoro-2,5-dioxo-2′,3′-dihydrospiro [imidazolidine-4,1′-inden]-1-yl]-N-[(4-fluorophenyl)methyl]-N-[1-methyl-3-(trifluoromethyl)azetidin-3-yl]acetamide.

7 . A pharmaceutical composition comprising the compound or the pharmaceutically acceptable salt thereof according to any one of claims 1 to 6 .

8 . A pharmaceutical composition comprising the compound or the pharmaceutically acceptable salt thereof according to any one of claims 1 to 6 , comprised as a combination with an additional drug, wherein the additional drug is at least one selected from the group consisting of a hormonal therapy agent, a chemotherapeutic agent, an immunotherapeutic agent, and an agent inhibiting a cell growth factor and a receptor action thereof.