FIELD: chemistry.
SUBSTANCE: compounds have c-Met inhibiting properties. In the formula I
B is absent, represents O, S, OCH2 or SCH2; each of the R1, R2, R3 and R4 independently represents hydrogen, halogen, unsubstituted C1-6alkyl, C1-6alkyl substituted by hydroxyl or 3-6 membered heterocyclyl with one heteroatom selected from N; carbamoyl; R1 and R2 or R3 and R4 form = O or cyclopropyl together; A represents N or CH; n equals 0, 1 or 2; each of the R5 independently represents halogen or unsubstituted C1-6alkyl; Z is NHR6 or is represented by formula II
,
where each of the R18 and R19 independently represents an unsubstituted C1-8alkyl or phenyl substituted by halogen; R6 is represented by formula
,
when R6 represented by formula VII, B represents O, S,OCH2 or SCH2; B1 represents
where each of the Q1 independently represents C(R7)2; B2 represents NHQ2, and Q2 represents phenyl substituted by halogen; Q3 represents hydrogen or phenyl substituted by halogen; each of the R7, R8, R9 and R10 independently represents hydrogen or phenyl substituted by halogen. The invention also relates to a pharmaceutical composition, to use of pharmaceutical composition to prepare a medical agent; to use of a compound to prepare a medical agent.
EFFECT: obtaining novel condensed derivatives of formula I, having a high inhibitory activity on c-Met.
36 cl, 2 tbl, 73 ex
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Authors
Dates
2017-05-12—Published
2013-07-01—Filed