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首页> 外文期刊>Chemistry of heterocyclic compounds >Synthesis and alkylation of N-Methylmorpholinium 4-Aryl-3-cyano-5-oxo-1,4, 5,6,7,8-hexahydroquinoline-2-selenolates
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Synthesis and alkylation of N-Methylmorpholinium 4-Aryl-3-cyano-5-oxo-1,4, 5,6,7,8-hexahydroquinoline-2-selenolates

机译:N-甲基吗啉鎓4-芳基-3-氰基-5-氧代-1,4,5,6,7,8-六氢喹啉-2-硒酸酯的合成和烷基化

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摘要

A multicomponent reaction of cyanoselenoacetamide with aromatic aldehydes, cyclohexane-1,3-dione, and N-methylmorpholine gave N-methylmorpholinium 4-aryl-3-cyano-5-oxo-1,4,5,6,7,8-hexahydro-quinoline-2-selenolates. Alkylation of the latter occurs under mild conditions with retention of the 1,4-dihydropyridine fragment to give 2-(2-R-methylseleno)-4-aryl-5-oxo-1,4,5,6, 7,8-hexahydro-quinoline-3-carbonitriles.
机译:氰基乙酰胺与芳族醛,环己烷-1,3-二酮和N-甲基吗啉的多组分反应生成N-甲基吗啉鎓4-芳基-3-氰基-5-氧代-1,4,5,6,7,8-六氢-喹啉-2-硒酸酯。后者的烷基化反应在温和的条件下进行,保留了1,4-二氢吡啶片段,得到2-(2-R-甲基硒基)-4-芳基-5-氧代-1,4,5,6,7,8-六氢喹啉-3-腈。

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