FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I)
,
where: ♦ R1 is a phenyl group, ♦ R2 is a hydrogen atom, ♦ R3 represents a hydrogen atom, a methyl group, -CH2-CH(CH3)2 group, -CH2-CF3 group, -C(O)-CH3 group, -C(O)-CH(CH3)2 group, -C(C-)-C(CH3)3 group, -C(O)-CH2-C(CH3)3 group, or -C(C-)-OC(CH3)3 group, ♦ n is an integer equal to 0, 1 or 2, ♦ W is a group
■ is
or ■ X is a carbon atom or a nitrogen atom, ■ R4 represents a hydrogen atom, a halogen atom, a linear or branched (C1-C6)alkyl group, a linear or branched (C2-C6)alkenyl group, a linear or branched (C2-C6)alkynyl group, -Y1-NR6R7 group, -Y1-OR6 group, a linear or branched halogen (C1-C6) alkyl group, an oxo group, -Y1-Cy1 group, -Cy1-R7 group, -Cy1-OR7 group or -Y1-NR6-C(O)-R7 group, ■ R5 represents a hydrogen atom, a halogen atom, a linear or branched (C1-C6)alkyl group, a piano group, or a hydroxy (C1-C6)alkyl group, ■ R6 represents a hydrogen atom, or a linear or branched (C1-C6)alkyl group, or -Y2-Si[(C1-C4)alkyl]3 group, ■ R7 is a hydrogen atom, a linear or branched (C1-C6)alkyl group or -Y2-Cy2 group, ■ Y1 and Y2 independently represent a bond or a linear or branched (C1-C4) alkylene group, ■ R8 represents a hydrogen atom or a linear or branched (C1-C6)alkyl group (other radical values are given in claim 1), which inhibits activity of USP7 protein, as well as containing pharmaceutical compositions and combinations thereof.
EFFECT: disclosed are novel piperidinyl derivatives, a method for preparing them and pharmaceutical compositions containing them.
23 cl, 1 tbl, 198 ex
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Authors
Dates
2021-02-15—Published
2017-06-09—Filed