FIELD: organic chemistry, pharmacy. SUBSTANCE: invention describes method of synthesis of 2-[2,4-difluorophenyl]-1,3-bis-[1H-1,2,4-triazole-2-ol (fluconazol) and its pharmaceutically acceptable salts. Method involves interaction of compound of the formula (IV) where R is hydrogen atom and Z is triazole with s-triazine. Fluconazol is an antifungal agent. Method ensures to prevent formation of nondesirable by-side products. EFFECT: improved method of synthesis, increased yield. 2 cl, 4 dwg, 25 ex
Authors
Dates
2001-07-20—Published
1996-12-20—Filed