首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Iodine-ammonium acetate promoted reaction between 2-aminopyridine and aryl methyl ketones: a novel approach towards the synthesis of 2-arylimidazo[1,2-a]pyridines
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Iodine-ammonium acetate promoted reaction between 2-aminopyridine and aryl methyl ketones: a novel approach towards the synthesis of 2-arylimidazo[1,2-a]pyridines

机译:碘乙酸铵促进2-氨基吡啶与芳基甲基酮之间的反应:合成2-芳基咪唑并[1,2-a]吡啶的新方法

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摘要

I-2-NH4OAc was found to be an efficient system for the metal-free synthesis of diversely substituted imidazo[1,2-a]pyridines 3a-r from 2-aminopyridine 1 and aryl methyl ketones 2a-r in one pot. 2-Arylimidazo[1,2-a]pyridines 3a-r were obtained in good to excellent yields via in situ generation of an Ortoleva-King intermediate (pyridinium iodide), followed by NH4OAc-assisted cyclization. (C) 2016 Elsevier Ltd. All rights reserved.
机译:发现I-2-NH4OAc是一种有效的系统,可在一锅中从2-氨基吡啶1和芳基甲基酮2a-r进行无金属合成多样化取代的咪唑并[1,2-a]吡啶3a-r。通过原位产生Ortoleva-King中间体(碘化吡啶),然后进行NH4OAc辅助环化,可以很好地获得2-Arylimidazoazo [1,2-a]吡啶3a-r。 (C)2016 Elsevier Ltd.保留所有权利。

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