FIELD: chemistry; pharmaceutics.
SUBSTANCE: invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof. In formula (I): X is selected from a group consisting of N and CH; R1 is hydrogen; R2 is selected from the group consisting of C1-6 alkyl, deuterated C1-6 alkyl, C3-6 cycloalkyl and C1-6 haloalkyl; R3 is -NR9(CH2)2NR9’R9’’; R4 is ; R5, R6 and R7 are independently selected from the group consisting of hydrogen and halogen; R8 is selected from the group consisting of hydrogen, C1-6 alkyl and C1-6 haloalkyl; R 9 is selected from a group consisting of hydrogen, C1-6 alkyl, deuterated C1-6 alkyl and C1-6 haloalkyl; R9' and R9'' are independently selected from the group consisting of hydrogen, C1-6 alkyl, C3-6 cycloalkyl, deuterated C1-6 alkyl and C1-6 haloalkyl, or R9' and R9'' together with a nitrogen atom bonded thereto, form a heterocycle, said heterocycle is unsubstituted or optionally substituted with 1–3 groups selected from the group consisting of halogen, C1-6 alkyl, C1-3 alkoxy, methylthio, methanesulfonyl and C1-6 haloalkyl; R10 is hydrogen and R11 is hydrogen.
EFFECT: disclosed compounds can selectively inhibit the activity of epidermal growth factor receptor (EGFR) mutants, demonstrate a high inhibitory effect on the EGFR mutant and antiproliferative activity against cancer cells and can be used for treating cancer.
2 cl, 1 dwg, 7 tbl, 1 ex
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Authors
Dates
2025-01-10—Published
2020-07-02—Filed