| 摘要 |
There is disclosed a process for the preparation of fluconazol which is a well-known antifungic agent, as well as pharmaceutically acceptable salts thereof, wherein a new compound having the formula (IV) in which R is H, benzyl, triphenylmethyl and COOR<1>, R<1> being alkyl or aryl, preferably terc-butyl or ethyl and Z is a triazol radical or hydrazine radical, optionally substituted by R, defined as above, optionally in the form of a salt, is reacted with s-triazine. The new compound (IV) is also an object of the invention.
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