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An efficient synthesis of imidazo[2,1-b][1,3,4] thiadiazol-7-ium hydroxides by a one-pot, three-component reaction in water

机译:通过一个罐,三分组分反应在水中有效合成咪唑诺[2,1-B] [1,3,4]噻二唑-7-Ium氢氧化物

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摘要

An improved synthesis of 2-ethyl-5-(2-hydroxy-4-oxoquinolin-3(4H)-ylidene)-6-aryl-5,6-dihydroimidazo[2,1-b][1,3,4]thiadiazol-7-ium hydroxide derivatives 4a-k via the reaction of aryl glyoxal monohydrates 1a-k, quinoline-2,4-diol 2 and 2-amino-[1,3,4]thiadiazole (3) in the presence of Et3N/sulfamic acid in H2O is described. This green protocol is characterized by the use of the readily available catalyst and reactants, short reaction times, operational simplicity and high yields of products. The structures of all compounds were characterized by H-1 NMR, C-13 NMR and Fourier-transform infrared (FT-IR) spectral data and microanalyses.
机译:改进的2-乙基-5-(2-羟基-4-氧代喹啉-3(4h) - 亚胺)-6-芳基-5,6-二氢咪唑[2,1-B] [1,3,4]的合成合成。 噻二唑-7-Ium氢氧化物衍生物4a-k通过芳基乙二醛单水合物1a-k,喹啉-2,4-二醇2和2-氨基-[1,3,4]噻二唑(3)在ET3N存在下 描述了H 2 O中的/氨基磺酸。 该绿色方案的特征在于使用易于使用的催化剂和反应物,反应时间短,操作简单性和高产率的产品。 所有化合物的结构都是通过H-1 NMR,C-13 NMR和傅立叶变换红外(FT-IR)光谱数据和微阳离子。

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