FIELD: organic chemistry.
SUBSTANCE: invention relates to organic chemistry, namely to a compound of formula (I) or to isomers thereof, where X1 and X2 each constitute ; R1 constitutes -NHR3, -NHCOR3, -NHSO2R3, -NHCOOR3, non-substituted 5-membered heteroaryl, wherein the non-substituted 5-membered heteroaryl in R1 contains three N atoms; R3 is independently selected from an atom of hydrogen, substituted or non-substituted C1-C4 alkyl, non-substituted 3-6-membered cycloalkyl, non-substituted 4-membered heterocyclyc group, non-substituted 5-6-membered heteroaryl; wherein said non-substituted 4-membered heterocyclyc group and said non-substituted 5-6-membered heteroaryl in R3 contain between one and three heteroatoms selected from N or O; the substituents in R3 are each independently selected from F, C1-C3 alkyle; R2 constitutes a non-substituted , non-substituted , non-substituted ; Y1 constitutes -S-, -S(=O)-, -S(O2)-, -C(F2)-; Y2 constitutes -O-; a, b, c, d, e and f each equals 1. The invention also relates to a method of synthesis of a compound of the formula (I), a pharmaceutical composition based on the compound of the formula (I) and application thereof.
EFFECT: technical result: new heterocyclic compounds are synthesized, said compounds useful in treatment and/or prevention of the microbial infection induced by Mycobacterium tuberculosis.
13 cl, 4 tbl, 39 ex
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Authors
Dates
2021-03-15—Published
2018-03-28—Filed