FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to method of synthesis and/or purification of clavulanic acid or its pharmaceutically acceptable salt or ester that involves the following stages: addition of additional solvent taken among -C1-C6-alcohols and their mixtures to clavulanic acid solution and water-nonmixable solvent; contact of solution with amine of the formula (I) where R1,R2,R3,R4 mean independently hydrogen atom, linear or branched C1-C8-alkyl, C2-C4,- hydroxyalkyl or groups NR1R2 and NR3R4 in common mean heterocyclic group containing 3-6 methylene groups possibly substituted with oxygen, sulfur atom or imino-group; R5 means hydrogen atom or methyl group; n is a whole number 1-3; isolation of formed clavulanic acid amine salt; and conversion of amine salt to clavulanic acid or its pharmaceutically acceptable salt or ester. Invention relates to also method of separation of clavulanic acid or its pharmaceutically acceptable salt or ester from impurity of clavam-2-carboxylic acid containing in filtered off broth using stages described above. EFFECT: new and simplified method of synthesis. 10 cl, 11 tbl, 15 ex
Authors
Dates
2001-05-10—Published
1996-04-17—Filed