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Cesium Carbonate as a Heterogeneous Base Catalyst for Synthesis of 2-Aminothiophenes via Gewald Reaction

机译:碳酸铯作为非均相催化剂,通过Gewald反应合成2-氨基噻吩

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摘要

The synthesis of substituted 2-amrnothiophenes is attractive to chemical researchers as they are important intermediates in organic synthesis and frequently used as the scaffold motif of a variety of agrochemicals, dyes, and biologically active products. Thus, because of their wide utility, researchers have synthesized the substituted 2-aminothiophenes via efficient and convenient methods. The one-pot cyclocondensation of ketones with an activated α-hydrogen, a cyanomethylene containing an electron-withdrawing group such as cyanoacetate and elemental sulfur in the presence of organic base, for example, morpholine, di-ethylamine, etc, known as the Gewald reaction, has been one of the most well-studied multicomponent reactions in recent years. To extend the scope of the reaction, many alterations have been made to the original Gewald's base-catalyzed, two-component combination of α-mercapto ketones with cyanoacetate by varying the components and the conditions.
机译:取代的2-氨苯并噻吩的合成对化学研究人员具有吸引力,因为它们是有机合成中的重要中间体,并经常用作多种农用化学品,染料和生物活性产品的骨架基序。因此,由于其广泛的用途,研究人员已经通过有效且方便的方法合成了取代的2-氨基噻吩。在有机碱(例如吗啉,二乙胺等)的存在下,将酮与活化的α-氢,含有吸电子基团的氰基亚甲基(如氰基乙酸酯和元素硫)进行一锅式环缩合反应是近年来研究最深入的多组分反应之一。为了扩大反应范围,已经通过改变组分和条件对原始的Gewald碱催化的α-巯基酮与氰基乙酸酯的两组分组合进行了许多改变。

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