Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5217118 | Tetrahedron | 2013 | 5 Pages |
Abstract
A simple and convenient synthesis of a novel series of pyrido[1,2-a]benzimidazoles was efficiently achieved from the condensation reactions of 1H-benzimidazol-2-ylacetonitrile (1) with some 3-substituted chromones, chromone-3-carboxylic acids, chromone-3-carboxamides, ethyl chromone-3-carboxylates and chromone-3-carbonitriles. Reaction of compound 1 with 2-aminochromone-3-carboxaldehydes produced 2-amino-3-(1H-benzimidazol-2-yl)chromeno[2,3-b]pyridines. The reaction mechanisms and spectral data were also discussed.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Magdy A. Ibrahim,