Issue 25, 2012

Study of N1-alkylation of indoles from the reaction of 2(or 3)-aminoindole-3-(or 2)carbonitriles with DMF-dialkylacetals

Abstract

The condensation of 2-aminoindole-3-carbonitriles and their 3-aminoindole-2-carbonitrile isomers with various DMF-dialkoxyacetals was investigated under microwaves. The appearance of reactive and versatile alkoxyiminium species allowed convenient access to indole precursors of building blocks with potential biological activity. The experimental results have been rationalised using DFT calculations of theoretical descriptors based on the electrostatic potential.

Graphical abstract: Study of N1-alkylation of indoles from the reaction of 2(or 3)-aminoindole-3-(or 2)carbonitriles with DMF-dialkylacetals

Supplementary files

Article information

Article type
Paper
Submitted
27 Jan 2012
Accepted
04 May 2012
First published
04 May 2012

Org. Biomol. Chem., 2012,10, 4916-4925

Study of N1-alkylation of indoles from the reaction of 2(or 3)-aminoindole-3-(or 2)carbonitriles with DMF-dialkylacetals

Y. Loidreau, S. Melissen, V. Levacher, C. Logé, J. Graton, J. Le Questel and T. Besson, Org. Biomol. Chem., 2012, 10, 4916 DOI: 10.1039/C2OB25747E

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