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首页> 外文期刊>Russian Journal of Organic Chemistry >Synthesis of Heterocyeles Based on Arylation Products of Unsaturated Compounds:XVII. Arylation of 2-Acetylfuran and Synthesis of 3-R-6-(5-Aryl-2-furyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines
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Synthesis of Heterocyeles Based on Arylation Products of Unsaturated Compounds:XVII. Arylation of 2-Acetylfuran and Synthesis of 3-R-6-(5-Aryl-2-furyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines

机译:基于不饱和化合物:XVII的芳基化产物的杂藻类化合物的合成。 2-乙酰基呋喃的丙烯酸化和3-R-6-(5-芳基-2-呋喃基)-7H- [1,2,4]三唑[3,4-b] [1,3,4]噻二嗪的合成

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摘要

Reaction of 2-acetylfuran with arenediazonium chlorides under Meerwein reaction conditions led to the formation of 5-aryl-2-acetylfurans.The bromination of these compounds gave 2-bromo-1-(5-aryl-2-furyl)-ethanones that reacted with 4-amino-4H-5-R-1,2,4-triazole-3-fhiols to form 3-R-6-(5-aryl-2-furyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines.
机译:在Meerwein反应条件下,2-乙酰基呋喃与氯化壬二唑反应导致生成5-芳基-2-乙酰基呋喃。这些化合物的溴化反应生成了2-溴-1-(5-芳基-2-呋喃基)-乙酮。与4-氨基-4H-5-R-1,2,4-三唑-3-酚形成3-R-6-(5-芳基-2-呋喃基)-7H- [1,2,4]三唑[3,4-b] [1,3,4]噻二嗪。

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