Compounds I ##STR1## where A equals CH or N; Ar equals naphthyl, thienyl or phenyl; R.sup.1 equals alkyl, F or Cl; g equals zero, 1 or 2; and Y equals various heterocyclic bases, and the acid-addition salts thereof, are described. Several preparation processes are described. The compounds IIIa ##STR2## where R.sup.1, g and Y are as specified in the case of the formula I, serve as intermediates for the preparation of these compounds. Processes are also specified for the preparation of IIIa. I represent valuable antimycotics.
描述了化合物I ##STR1## 其中A等于CH或N; Ar等于
萘基,
噻吩基或苯基; R.sup.1等于烷基,F或Cl; g等于零,1或2; Y等于各种杂环碱及其酸加成盐。描述了几种制备过程。化合物IIIa ##STR2## 其中R.sup.1,g和Y如公式I所述,用作这些化合物的制备中间体。还指定了IIIa的制备过程。I代表有价值的抗真菌药物。