申请人:Shionogi & Co., Ltd.
公开号:US04612322A1
公开(公告)日:1986-09-16
A compound of the formula: ##STR1## (wherein Az is imidazolyl or triazolyl; R is C.sub.1 -C.sub.5 alkyl or phenyl optionally substituted by 1 to 3 members selected from halogen, C.sub.1 -C.sub.5 alkyl, and C.sub.1 -C.sub.5 alkoxy; X.sup.1 and X.sup.2 each is hydrogen, halogen, C.sub.1 -C.sub.5 alkyl, or C.sub.1 -C.sub.5 alkoxy; Y is C.dbd.O, C.dbd.S, S.dbd.O, or R.sup.1 --C--R.sup.2 ; and R.sup.1 and R.sup.2 each is hydrogen, C.sub.1 -C.sub.3 alkyl or, taken together may form C.sub.4 -C.sub.6 alkylene) or its acid addition salt being useful as an antimycotic agent is prepared by reacting a corresponding diol with a cyclizing agent.
以下化合物的公式:##STR1##(其中Az是咪唑基或三唑基;R是C.sub.1-C.sub.5烷基或苯基,可选地取代1至3个来自卤素,C.sub.1-C.sub.5烷基和C.sub.1-C.sub.5烷氧基的成员;X.sup.1和X.sup.2分别是氢,卤素,C.sub.1-C.sub.5烷基或C.sub.1-C.sub.5烷氧基;Y是C.dbd.O,C.dbd.S,S.dbd.O或R.sup.1--C--R.sup.2;R.sup.1和R.sup.2分别是氢,C.sub.1-C.sub.3烷基或一起形成C.sub.4-C.sub.6烷基)或其酸加成盐,作为抗真菌剂是通过将相应的二醇与环化剂反应制备的。