Synthetic Communications ( IF 2.1 ) Pub Date : 2021-01-08 Gurpreet Kaur, Radha Moudgil, Mussarat Shamim, Vivek Kumar Gupta, Bubun Banerjee
Abstract
A simple, mild, eco-friendly, general, and convenient approach has been developed for the synthesis of structurally diverse 2-arylbenzothiazole derivatives from the reactions of 2-aminothiophenol and various aromatic aldehydes using camphor sulfonic acid a low cost, commercially available, efficient organo-catalyst in aqueous ethanol at room temperature. Under the same optimized conditions, a series of 2-arylbenzimidazoles was also synthesized starting from o-phenylenediamines and various aldehydes whereas synthesis of 3H-spiro[benzo[d]thiazole-2,3′-indolin]-2′-ones was accomplished from the reactions of 2-aminothiophenol and substituted isatins.
中文翻译:
樟脑磺酸在室温下催化简单,容易且通用的合成2-芳基苯并噻唑,2-芳基苯并咪唑和3H-螺[苯并[d]噻唑-2,3'-吲哚] -2'-的方法。
摘要
已经开发了一种简单,温和,环保,通用且方便的方法,用于使用樟脑磺酸由2-氨基硫酚与各种芳族醛的反应合成结构多样的2-芳基苯并噻唑衍生物。有机催化剂在室温下于乙醇水溶液中。在相同的优化条件下,还从邻苯二胺和各种醛开始合成了一系列的2-芳基苯并咪唑,而合成了3 H-螺[苯并[ d ]噻唑-2,3'-吲哚] -2'-一个。由2-氨基苯硫酚与取代的靛红的反应完成。