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乙炔基乙烯酮 - S,S - 缩醛:高反应活性的富电子亲双烯体及其在通过一锅三组分反应合成4 - 官能化喹啉中的应用。

Ethynyl ketene-S,S-acetals: the highly reactive electron-rich dienophiles and applications in the synthesis of 4-functionalized quinolines via a one-pot three-component reaction.

作者信息

Zhao Yu-Long, Zhang Wei, Wang Shuang, Liu Qun

机构信息

Department of Chemistry, Northeast Normal University, Changchun, 130024, People's Republic of China.

出版信息

J Org Chem. 2007 Jun 22;72(13):4985-8. doi: 10.1021/jo070069q. Epub 2007 May 25.

Abstract

An efficient synthetic method for 4-functionalized quinoline derivatives, 4-((1,3-dithian-2-ylidene)methyl)quinolines, has been developed. Mediated by trifluoromethanesulfonic acid, ethynyl ketene-S,S-acetals can react in a one-pot procedure with various arylamines and aldehydes under mild conditions to give the corresponding quinoline derivatives in good to high yields via a consecutive arylimine formation, regiospecific aza-Diels-Alder (Povarov) reaction, and reductive amination.

摘要

已开发出一种用于合成4-官能化喹啉衍生物4-((1,3-二硫杂环戊烯-2-亚基)甲基)喹啉的有效方法。在三氟甲磺酸介导下,乙炔基乙烯酮-S,S-缩醛可在温和条件下与各种芳胺和醛一锅反应,通过连续形成芳基亚胺、区域特异性氮杂狄尔斯-阿尔德(波瓦罗夫)反应和还原胺化反应,以良好至高产率得到相应的喹啉衍生物。

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