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首页> 外文期刊>American Chemical Society >Synthesis of Functionalized 2-Aminohydropyridines and 2-Pyridinones via Domino Reactions of Arylamines, Methyl Propiolate, Aromatic Aldehydes, and Substituted Acetonitriles
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Synthesis of Functionalized 2-Aminohydropyridines and 2-Pyridinones via Domino Reactions of Arylamines, Methyl Propiolate, Aromatic Aldehydes, and Substituted Acetonitriles

机译:通过芳基胺,丙酸甲酯,芳香醛和取代的乙腈的多米诺反应合成功能化的2-氨基氢吡啶和2-吡啶酮

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摘要

An efficient and practical synthetic method for the functionalized 2-amino hydropyridines and 2-pyridinones was successfully developed via the domino reactions of arylamines, methyl propiolate, aromatic aldehydes and the substituted acetonitriles with triethylamine as base catalyst. Reactions involving malononitrile and cyanoacetamide gave exclusively the 2-aminohydropyridines. On the other hand ethyl cyanoacetate resulted in the 2-pyridinones as main products.Keywords: dihydropyridine; 2-pyridinone; electron-deficient alkyne; β-enamino ester; domino reaction
机译:通过芳基胺,丙酸甲酯,芳族醛和取代的乙腈与三乙胺作为基础催化剂的多米诺反应,成功开发了一种功能化的2-氨基氢吡啶和2-吡啶酮的高效实用合成方法。涉及丙二腈和氰基乙酰胺的反应仅产生2-氨基氢吡啶。另一方面,氰基乙酸乙酯产生了2-吡啶基酮为主要产物。 2-吡啶酮;缺电子炔烃β-烯胺酯;多米诺骨牌反应

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