FIELD: chemistry.
SUBSTANCE: invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof. In formula (I) the values of radicals are as follows: R1 is cyclopropyl substituted with one or two halogen groups; R2 and R3 are -H; R4 is selected from a group consisting of 6-membered aryl, ,
,
,
and
, wherein said 6-membered aryl is optionally substituted with one to three groups selected from the group consisting of halogen, hydroxyl, C1-C12alkyl, C3-C12cycloalkyl, C1-C12haloalkyl, C1-C12hydroxyalkyl, C1-C12alkoxy-C1-C12alkyl, C1-C12alkoxy-C1-C12alkoxy, di-C1-C12alkylaminoC1-C12alkyl, -CH2NHC(O)CH3, -NRaRb, -NRaC(=O)Rb, -ORa, -CN, -C(=O)Ra, -C(=O)ORa, -SRa, furanyl, pyrrolyl and pyrazolyl; Ra and Rb independently represent -H or C1-C12alkyl; R5 is H, halogen or C1-C12alkyl. Also disclosed is a compound selected from a group of individual compounds specified in the claim, and a pharmaceutical composition containing said compounds.
EFFECT: disclosed compounds are c-abl and/or LRRK2 kinase inhibitors and can be used to treat neurodegenerative diseases.
24 cl, 2 tbl, 14 ex
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Authors
Dates
2025-01-14—Published
2020-02-21—Filed