FIELD: biologically-active compounds. SUBSTANCE: invention provides naphthiridone carboxylic acid salts having formula I: (I) wherein R'H is pharmaceutically acceptable acid selected from group including R4SO3H, R4PO3H, and YH, R4 is C1-C6-alkyl and optionally C1-C6-alkyl-substituted phenyl or naphthyl, and Y is chlorine atom or nitrate residue. Compounds I are prepared by bringing compound of formula II: (II), wherein R2 is (C1-C6)-alkyl, aryl-(C1-C6)-alkyl, or hydrogen, and P3 is nitro group, into reaction with reduction agent optionally in presence of compound R'H (R' as defined above) and then, if necessary, reaction product is affected by compound R'H, the same or other than that in reduction reaction. Reaction intermediates show antibacterial activity. EFFECT: simplified procedure. 34 cl, 5 ex
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