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PhP/I 介导的由芳基异硫氰酸酯合成 N,N',N″-取代的胍和 2-亚氨基咪唑啉-4-酮。

PhP/I-Mediated Synthesis of N,N',N″-Substituted Guanidines and 2-Iminoimidazolin-4-ones from Aryl Isothiocyanates.

机构信息

Department of Chemistry, Faculty of Science, ‡Graduate School, §Center of Excellence in Materials Science and Technology, and ∥Center of Excellence for Innovation in Chemistry, Faculty of Science, Chiang Mai University , Chiang Mai 50200, Thailand.

出版信息

J Org Chem. 2017 Oct 6;82(19):10331-10340. doi: 10.1021/acs.joc.7b01794. Epub 2017 Sep 12.

Abstract

A convenient one-pot procedure for the synthesis of acyclic and cyclic guanidines mediated by the PhP/I system is described. Sequential condensation of aryl isothiocyanates with amines followed by dehydrosulfurization and guanylation could lead to both symmetric and unsymmetric N,N',N″-substituted derivatives. Through a tandem guanylation-cyclization, a series of 2-iminoimidazolin-4-ones could also be prepared in good yields from the reaction of aryl isothiocyanates with amino acid methyl esters.

摘要

描述了由 PhP/I 体系介导的无环和环状胍的方便一锅法合成。芳基异硫氰酸酯与胺的顺序缩合,然后进行脱水脱硫和胍化,可以得到对称和不对称的 N,N′,N″-取代衍生物。通过串联的胍化-环化反应,芳基异硫氰酸酯与氨基酸甲酯反应也可以以良好的收率得到一系列 2-亚氨基咪唑啉-4-酮。

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