FIELD: chemistry.
SUBSTANCE: invention relates to a compound of formula (II), (III), (IV) or (V), or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof. In the above formulas, the values of the variables are as follows: G is selected from a group consisting of an optionally substituted C6-aryl, optionally substituted 5–6 membered heteroaryl having one or more heteroatoms selected from N and S, optionally substituted 5–8 membered heterocyclyl having one or more heteroatoms selected from O and N, C2-C10 alkynyl and a direct bond; L is selected from a group consisting of –CH=, -CHR4-, -(CH2)q-, -NR5-, -O-, -O(CH2)q-, -C(O)-, -C(O)(CH2)q-, -SO2- and direct communication, in which each q is individually and independently integer from 1 to 4; Z is selected from the group consisting of hydrogen, deuterium, halogen, C1-C4 alkyl, C1-C4 alkylamine, C1-C4 dialkylamine and optionally substituted 4–7 membered heterocyclyl or a heterocyclic spiro compound; R1 is selected from a group consisting of hydrogen and deuterium; R2 is selected from the group consisting of hydrogen, deuterium, halogen and C1-C6 alkyl; R3 is selected from the group consisting of hydrogen, deuterium and C1-C6 alkyl; R4 is selected from the group consisting of deuterium and C1-C6 alkyl; and R5 is selected from the group consisting of hydrogen and C1-C6 alkyl. Also disclosed is a pharmaceutical composition containing said compound, and a method of treating using said compound.
EFFECT: disclosed compounds inhibit RTK class III kinases, such as kinases FLT3, PDGFR, and can be used to treat diseases or disorders mediated by such kinases, particularly cancer.
10 cl, 7 tbl, 6 ex
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Authors
Dates
2025-01-13—Published
2020-08-22—Filed