使用 N,N-二甲基乙酰胺作为亲电碳源合成 N-杂环化合物。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Dayoung Chun, Seok Beom Lee, Simin Chun, Seung Hyun Choi, Junhwa Hong, Honghui Lee, Jinwoo Lee and Suckchang Hong
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引用次数: 0

摘要

本研究使用含氮亲核底物和来自 N,N-二甲基乙酰胺(DMAc)的亲电碳源合成了 N-杂环化合物。根据亲核基团的不同,生成了 4-喹唑啉酮、吡咯-喹喔啉和二氢苯并噻二嗪二恶英等 N 型杂环化合物。在 FeCl3-6H2O 和二叔丁基过氧化物(DTBP)的作用下,DMAc 中与氮相邻的碳被活化。这一过程被认为是一种经济的合成方法,因为它利用了铁催化剂和 DMAc 作为亲电碳源和溶剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis of N-heterocyclic compounds using N,N-dimethylacetamides as an electrophilic carbon source†

Synthesis of N-heterocyclic compounds using N,N-dimethylacetamides as an electrophilic carbon source†

In this study, N-heterocyclic compounds were synthesized using nitrogen-containing nucleophilic substrates and electrophilic carbon sources derived from N,N-dimethylacetamide (DMAc). Depending on the nucleophilic groups, N-heterocyclic compounds such as 4-quinazolinones, pyrrole-quinoxalines, and dihydro-benzothiadiazine dioxides were produced. Carbon, adjacent to the nitrogen in DMAc, was activated in the presence of FeCl3·6H2O and di-t-butyl peroxide (DTBP). This procedure was considered an economical synthetic method because it utilized iron catalysts and DMAc as an electrophilic carbon source and a solvent.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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