| abstract |
A process for the preparation of fluconazole, which is a well blown antifungal agent,nand of pharmaceutically acceptable salts thereof is disclosed, wherein a novel compoundnof the formula (IV)n nwherein R represents H, benzyl, triphenylmethyl and COOR 1 with R 1 being alkyl ornaryl, preferably tert-butyl or ethyl, and Z represents a triazole radical or hydrazinenradical optionally substituted by R being defined as above, optionally in the salt form,nis reacted with s-triazine. The novel compound (IV) is an object of the invention asnwell. |