FIELD: organic chemistry.
SUBSTANCE: invention relates to a compound of formula (1) or a pharmaceutically acceptable salt thereof, wherein one of Y and Z is R3 and the other is Ar2; Q1 is C1-4 alkylene group, optionally containing one substitute selected from hydroxy, provided that, in the presence of a hydroxy substituent between the hydroxy substituent and the nitrogen atom to which Q2 is bonded, there are at least two carbon atoms; Q2 represents a bond or C1-3 alkylene group; R1 is selected from hydrogen, NRxRy and Cy1 group; Rx and Ry are identical or different and each represents C1-4 alkyl; Cy1 is C-linked morpholine; all R2, R3 and R4 are hydrogen; Ar1 is a phenyl ring optionally containing 1 or 2 substituents R5, which are identical or different and are selected from a halogen and a group Ra-Rb; Ra is a bond, O or NRcSO2; Rb is selected from hydrogen, C1-8 alkyl group; Rc is hydrogen; and Ar2 is 5.6 a condensed heteroaromatic ring, containing 2, 3 or 4 nitrogen atoms as heteroatomic ring members, optionally containing 1 substituent R7, selected from C1-4 alkyl and cyano. Invention also relates to specific derivatives of the compound of formula (1), a pharmaceutical composition based on the compound of formula (1), a method of treating said diseases and use of the compound of formula (1).
EFFECT: obtaining novel heterocyclic compounds having P70S6K inhibitor properties.
12 cl, 4 dwg, 44 ex
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Authors
Dates
2020-11-11—Published
2016-09-30—Filed