Synthesis of novel fused thienodiazaphosphorine derivatives from 2-amino-3-cyanothiophenes and Lawesson's reagent

被引：11

作者：

Khalladi, Khaoula ^{[1
]}

Touil, Soufiane ^{[1
]}

机构：

[1] Univ Carthage, Dept Chem, Fac Sci Bizerta, Lab Heteroatom Organ Chem, Jarzouna 7021, Tunisia

来源：

JOURNAL OF SULFUR CHEMISTRY | 2012年 / 33卷 / 01期

关键词：

thiophenes; diazaphosphorines; Lawesson's reagent; thienodiazaphosphorines; fused heterocycles; Dimroth rearrangement; AMINOPHOSPHONOTHIOPHENE DERIVATIVES; BIOLOGICAL EVALUATION; GEWALD REACTION; 2-OXIDES; REACTIVITY; THIOPHENE; ACIDS;

D O I：

10.1080/17415993.2011.639021

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

In a simple one-pot procedure, treatment of 2-amino-3-cyanothiophenes with Lawesson's reagent (LR) leads to the new thieno[2,3-d][1,3,2]diazaphosphorine-6-thione-2-sulfides in good to excellent yields. A possible reaction mechanism, involving a Dimroth-type rearrangement, is proposed. The structure of obtained products was confirmed by NMR (H-1, P-31, and C-13) and IR spectroscopies and by mass spectrometry. [GRAPHICS] .

引用

页码：27 / 32

页数：6

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