1-Ethyl-imidazoles of the formula ##SPC1## Or a pharmaceutically acceptable nontoxic salt thereof, are produced by A. reacting a compound of the formula ##SPC2## With imidazole; or B. when R.sup.1 is hydrogen, reacting a compound of the formula ##SPC3## With imidazole in the presence of an acid binding agent. In the case of the salts the free base produced is reacted with an appropriate acid. The 1-ethyl-imidazoles are useful for their antimycotic activity.
公式为##
SPC1##的
1-乙基咪唑,或其药学上可接受的无毒盐,可通过以下方法制备:A.将公式为##
SPC2##的化合物与
咪唑反应;或B.当R.sup.1为氢时,在酸性结合剂的存在下将公式为##
SPC3##的化合物与
咪唑反应。对于盐的情况,将产生的自由碱基与适当的酸反应。
1-乙基咪唑由于其抗真菌活性而有用。