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Synthesis of 4-Halofuro[3,4- c ]pyridin-3(1 H )-ones from 2-Halopyridine-3,4-dicarbonitriles
Russian Journal of Organic Chemistry ( IF 0.8 ) Pub Date : 2020-10-19 , DOI: 10.1134/s1070428020090067
S. V. Fedoseev , M. Yu. Belikov , O. V. Ershov , V. A. Tafeenko

Abstract

Heating of 2-halopyridine-3,4-dicarboxylic acids in propionic anhydride led to the formation of 4-halofuro[3,4-c]pyridine-1,3-diones as a result of intramolecular dehydration of the vicinal carboxy groups. The subsequent reduction of 4-halofuro[3,4-c]pyridine-1,3-diones with sodium tetrahydridoborate in THF at room temperature afforded 4-halofuro[3,4-c]pyridin-3(1H)-ones as the major products.



中文翻译:

从2-卤代吡啶-3,4-二甲腈合成4-卤代呋喃并[3,4-c]吡啶-3(1 H)-一

摘要

由于邻位羧基的分子内脱水,在丙酸酐中加热2-卤代吡啶-3,4-二羧酸导致4-卤代呋喃并[3,4- c ]吡啶-1,3-二酮的形成。随后在室温下用四氢硼酸钠在THF中还原4-卤代呋喃并[3,4- c ]吡啶-1,3-二酮,得到4-卤代呋喃并[3,4- c ]吡啶-3(1 H)-主要产品。

更新日期:2020-10-19
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