FIELD: organic chemistry.
SUBSTANCE: invention relates to a heterocyclic compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein X is selected from a group consisting of NR6 and O; R1 and R2 are independently selected from a group consisting of hydrogen, halogen, C1-4 alkyl; R3 is C1-4 alkoxy; R4 is selected from a group consisting of [2-(dimethylamino)ethyl](methyl)amino and (2-hydroxyethyl)(methyl)amino; R5 is selected from a group consisting of hydrogen and C1-3 alkoxy C1-3 alkyl; R6 is selected from a group consisting of hydrogen and C1-4 alkyl. Invention also relates to a pharmaceutical composition based on a compound of formula (I) or a pharmaceutically acceptable salt thereof, a method of treating said diseases and using the compound of formula (I) or a pharmaceutically acceptable salt thereof or a pharmaceutical composition based thereon.
EFFECT: obtaining novel heterocyclic compounds having the properties of EGFR inhibitor and double mutant EGFR-L858R/T790M, useful in treating malignant lung tumor, including non-small-cell lung cancer, small-cell lung cancer, lung adenocarcinoma and squamous cell lung cancer.
12 cl, 2 tbl, 15 ex
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Authors
Dates
2020-10-23—Published
2016-07-15—Filed