New Method of Synthesis of Biologically Active Get(aryl)chalcogenylacetates of Tris(2-hydroxyethyl)ammonium
作者:S. N. Adamovich、Е. N. Oborina、I. А. Ushakov、А. N. Mirskova
DOI:10.1134/s1070363218100353
日期:2018.10
Physiologically and pharmacologically active het(aryl)chalcogenylacetates of tris(2-hydroxyethyl)ammonium of pharmacopeial purity have been synthesized by the reaction of het(aryl)chalcogenylacetic acids with sodium (potassium) hydroxide and triethanolamine hydrochloride by one-pot method in quantitative yield (up to 99.8%).
通过一锅法使杂芳基
硫属酰基
乙酸与
氢氧化钠(
钾)和
三乙醇胺盐酸盐反应,定量合成了药理学纯度的三(2-羟乙基)
铵的生理和药理学活性的杂芳基
硫属
乙酸酯。 (高达99.8%)。