Issue 23, 2009

Synthesis of novel synthetic intermediates from the reaction of benzimidazole and triazolecarbenes with ketenimines and their application in the construction of spiro-pyrroles

Abstract

2-(2-Alkoxycarbonyl-1-arylamino-1-propenyl)benzimidazolium and 5-(2-alkoxycarbonyl-1-arylamino-1-propenyl)triazolium salts were synthesized in good yields from the reaction of benzimidazole and triazole carbenes with ketenimines. Upon treatment with a base, both salts were converted into novel 1,3-dipoles which underwent [3+2] cycloaddition reactions with electron-deficient alkynes and allenes to produce benzimidazole-spiro-pyrroles or triazole-spiro-pyrroles. This work provides novel synthons for the construction of multifunctional spiro-pyrrole derivatives that are not easy accessible by other synthetic methods and are potentially amenable to further transformations.

Graphical abstract: Synthesis of novel synthetic intermediates from the reaction of benzimidazole and triazole carbenes with ketenimines and their application in the construction of spiro-pyrroles

Supplementary files

Article information

Article type
Paper
Submitted
27 Jul 2009
Accepted
14 Sep 2009
First published
14 Oct 2009

Org. Biomol. Chem., 2009,7, 5010-5019

Synthesis of novel synthetic intermediates from the reaction of benzimidazole and triazole carbenes with ketenimines and their application in the construction of spiro-pyrroles

J. Mo, Y. Ma and Y. Cheng, Org. Biomol. Chem., 2009, 7, 5010 DOI: 10.1039/B915215F

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