ALKYNYL-SUBSTITUTED HETEROCYCLIC COMPOUND, METHOD FOR PRODUCTION THEREOF AND USE THEREOF IN MEDICINE Russian patent published in 2020 - IPC C07D231/14 C07D231/44 C07D401/04 C07D401/06 C07D401/14 C07D403/04 C07D403/06 C07D403/14 A61K31/4155 A61K31/454 A61P35/00 

Abstract RU 2729069 C1

FIELD: chemistry.

SUBSTANCE: invention relates to organic chemistry and specifically to a compound of formula (II), or an isomer thereof, or a pharmaceutically acceptable salt thereof:

.

In formula II: R1 denotes H or -NHR3; R3 represents H, C1-6 alkyl or 4–6 membered heterocyclyl, wherein alkyl and heterocyclyl is optionally substituted with halo, -OR5, C1-6 alkyl, C3-6 cycloalkyl, or 4–6 membered heterocyclyl; X is absent or represents C1-6 alkylene; Y is absent or is C3-6 cycloalkylene or 4–6-member heterocyclylene; Z is cyano,

bond a is a double bond or triple bond; in the event that said bond is a double bond, each Ra, Rb and Rc are independently H, halogen or C1-6 alkyl, wherein alkyl is optionally substituted with -OC1-2 alkyl or -N(C1-2 alkyl)2; in the event that said bond is a triple bond, Ra and Rc are absent and Rb is H or C1-6 alkyl; Ga, Gb, Gc and Gd, each independently selected from a group consisting of H, halogen, -OR5 and -C(O)NR6R7; R4, R5, R6 and R7, each independently represent H or C1-6 alkyl, wherein n in formula II is optionally substituted by 2N. Also presented is a pharmaceutical composition and a method of treating.

EFFECT: technical result: novel organic compounds acting as fibroblast growth factor receptor (FGFR) inhibitor.

11 cl, 2 tbl, 34 ex

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RU 2 729 069 C1

Authors

Chen, Xiangyang

Gao, Insiangao, Yingxiang

Kong, Norman Xianglong

Dates

2020-08-04Published

2017-01-25Filed