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US 2026/0216197 A1Published application
Wrn helicase inhibitor
AssigneeSuzhou Puhe Biopharma Co., Ltd.
InventorsBin Liu, Feng Gao, Yongqi Guo, Yongyong Wu, Liandong Jing, Zhizhong Li, Zhuo Wu
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Abstract
The present invention provides a WRN helicase inhibitor as represented by the compound in formula (I) or a pharmaceutically acceptable salt, isotopic variant, tautomer or stereoisomer thereof.
Claims16
A compound of formula (I), or a pharmaceutically acceptable salt, isotopic variant, tautomer, or stereoisomer thereof:
- wherein,
- represents a single bond or a double bond;
- X and Y are each independently selected from CH and N, and at least one of X and Y is N;
- R1 is selected from
- alternatively, R1 is selected from
- and the R1 is optionally substituted with 1 or 2 Rx;
- R2 is selected from H, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 alkylthio and C3-6 cycloalkyl;
- R3 is independently selected from H, halogen, CN, C1-6 alkyl, C1-6 haloalkyl and C3-6 cycloalkyl;
- or two R3 on the same or different carbon atoms are connected to form a 3- to 6-membered spiro or bridged ring;
- R4 is independently selected from H, halogen, CN, SF5, —SCF3, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkylthio, C3-6 cycloalkyl and 4- to 10-membered heterocyclyl;
- Ring A and the benzene ring to which it is connected together form a fused ring, and Ring A is selected from 5- to 6-membered heteroaryl and 5- to 7-membered heterocyclyl;
- R5 is selected from H, halogen, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 alkylthio and C3-6 cycloalkyl;
- Rx is selected from H, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, CN, NH2, —C(O)Ra, —C(O)ORa, —(CH2)p—ORa, —P(O)—(Ra)2 and —S(O)2—Ra;
- Ra is selected from H, C1-6 alkyl and C3-6 cycloalkyl;
- m is selected from 0, 1, 2 and 3;
- n is selected from 0, 1 and 2;
- p is selected from 0, 1 and 2.
14 more elements
A compound, or a tautomer, stereoisomer or pharmaceutically acceptable salt thereof, wherein the compound is selected from:
(canceled)
(canceled)
Dependencies are inferred from the claim text.