首页> 美国卫生研究院文献>Beilstein Journal of Organic Chemistry >One-pot synthesis of substituted pyrrolo34-bpyridine-45-diones based on the reaction of N-(1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-2-oxo-2-arylethyl)acetamide with amines
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One-pot synthesis of substituted pyrrolo34-bpyridine-45-diones based on the reaction of N-(1-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)-2-oxo-2-arylethyl)acetamide with amines

机译:基于N-(1-(4-羟基-6-甲基-2-氧-2-氧-2H-吡喃-3-)的反应一锅合成取代的吡咯并34-b吡啶-45-二酮胺基)-2-氧代-2-芳基乙基)乙酰胺

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摘要

The condensation of primary amines with -(1-(4-hydroxy-6-methyl-2-oxo-2 -pyran-3-yl)-2-oxo-2-arylethyl)acetamides was explored. Thus, a previously unknown recyclization of the starting material was observed in acidic ethanol in the presence of an amine, which provided the corresponding dihydropyrrolone derivative as the major reaction product. Based on this transformation, a practical and convenient one-pot synthetic method for substituted pyrrolo[3,4- ]pyridin-5-ones could be devised.
机译:研究了伯胺与-(1-(4-羟基-6-甲基-2-氧代-2-吡喃-3-基)-2-氧代-2-芳基乙基)乙酰胺的缩合。因此,在胺存在下在酸性乙醇中观察到原料的先前未知的再循环,这提供了相应的二氢吡咯烷酮衍生物作为主要反应产物。基于这种转化,可以设计出一种实用,方便的一锅合成吡咯并[3,4-]吡啶-5-酮的方法。

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