Da Settimo A, Livi O, Biagi G, Primofiore G, Masoni G
Farmaco Sci. 1982 Nov;37(11):728-39.
Several 1,2,3-triazolederivatives of aryloxyalcanoic acids of general formula (II) were synthesized. Some derivatives were obtained by the cycloaddition reaction of 4-azidophenoxyacetic acid (III) to activated methylene compounds, but the largest part were prepared by nucleophilic substitution reactions of three new (4-hydroxyphenyl)triazole derivatives and alyphatic bromoesters. Some compounds, tested as prostaglandin-synthetase inhibitors of rat spleen in vitro, showed practically no activity; moderate activities as herbicides, insecticides and antimicrobials were detected.
合成了通式(II)的几种芳氧基链烷酸的1,2,3 - 三唑衍生物。一些衍生物是通过4-叠氮苯氧基乙酸(III)与活性亚甲基化合物的环加成反应得到的,但大部分是通过三种新型(4-羟基苯基)三唑衍生物与脂肪族溴代酯的亲核取代反应制备的。一些化合物在体外作为大鼠脾脏前列腺素合成酶抑制剂进行测试时,几乎没有活性;检测到它们作为除草剂、杀虫剂和抗菌剂具有中等活性。