FIELD: organic chemistry, heterocyclic compounds. SUBSTANCE: invention describes derivatives of imidazopyridine of the general formula (I):
where X is CH or N; Z means -CH=CH or S; A means -CH2CH2, CH=CH, CH(OH)-CH2 or CO-CH2; B means directed bond or -CH2-,-CH(CH3)2- or when Z means CH=CH. B can form cyclopentane ring fused with the bound benzene ring; Y completes the condensed benzo- or thienyl ring that is substituted optionally with haloid- or C1-C4-alkyl; n = 0, 1 or 2 and m = 0 or 1. Synthesized compounds are antagonists of both ТАФ and histamine H1, and can be used for treatment of patients with allergic inflammatory diseases (allergic rhinitis). Invention describes also a method of synthesis of derivatives of imidazopyridine of the formula (I)
and pharmaceutical composition based on thereof. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 15 cl, 3 tbl
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