FIELD: organic chemistry, heterocyclic compounds. SUBSTANCE: invention describes the novel compounds, phenyloxazolidinones substituted with heteroaromatic rings in ring of the formula (Ia) or its pharmaceutically acceptable salts where: Q means heteroaromatic 5-membered ring bound with aromatic ring (1) in nitrogen atom of the structural formulas: (Ia), (I) , (II) , (III) , (IV) , (V) , (VI) , (VII) , (VIII) or (IX) or in other variant Q can mean heteroaromatic 5-membered ring condensed with benzene and bound with aromatic ring (1) of the structural formula (X) ; R1 means independently H, F or Cl; R2 means independently C1-C8-alkyl optionally substituted with one or more atoms of F or Cl; R3 each is taken independently among of: (a) H; (b) OR4; (c) SR4; (d) NHSO2R4; (e) CO2R4; (f) COR4; (g) saturated or unsaturated C1-C8-alkyl that can be direct or branched and optionally substituted with one or more substituent taken among of (e), (j) -C(R5)=NR6 where R5 means C1-C6-alkyl and R6 means OH orOC1-C6 OC1-C6-alkyl; R4 means: (a) H; (b) C1-C6-direct or branched alkyl chain. These compounds are useful antibacterial agents showing activity against human and animal pathogens including gram-positive aerobic bacteria, for example, multiple-resistant staphylococci, streptococci and enterococci and also anaerobic microorganisms, for example, Bacteroides spp. , Clostridium spp. and acid-fast microorganisms, for example, Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp. EFFECT: new compounds indicated above, valuable antibacterial properties. 11 cl, 8 dwg, 1 tbl
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Authors
Dates
2000-08-20—Published
1996-01-29—Filed