FIELD: chemistry.
SUBSTANCE: invention relates to 1,3,4-oxadiazolamide derivative represented by following formula I, stereoisomer or pharmaceutically acceptable salt thereof, where L1, L2 or L3 each independently represent a bond or -(C1-C2 alkylene)-; Z1 - Z4 each independently represent N or CRZ, where three or four of Z1 - Z4 each independently represents CRZ, and RZ is -H or -X; R1 is -CX2H or -CX3; R2 is -(C1-C4 alkyl), -(C3-C6 cycloalkyl), -phenyl, pyridinyl, or . Y is -N-, -O- or -S(=O)2-, when Y is -N-, R4 and R8 each independently represent -H, -(C1-C4 alkyl), -C(=O)-(C1-C4 alkyl), -C(=O)-(C3-C6 cycloalkyl), -C(=O)-O(C1-C4 alkyl), -C(=O)-CF3, -S(=O)2-(C1-C4 alkyl), -oxetanyl or benzyl, and when Y is -O- or -S(=O)2-, R4 and R8 are absent; R5 -R8 each independently represent -H, - (C1-C4 alkyl), -OH, -CH2OH or -C(=O)-NH2, and a - c each independently represent an integer having value of 1 or 2; R3 is phenyl, -phenyl, which can be substituted with -X, and X is F, Cl, Br or I.
(I).
EFFECT: compounds of the invention are intended for preparing a drug for treating histone deacetylase of 6-mediated disease.
10 cl, 2 tbl, 101 ex
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