Paper
Synthesis and Structural Studies of (2-Oxo-2,3-dihydroimidazo[1,2-a]-pyridin-3-yl)acetic Acids
Published 2004 · W. Chui, A. Dolzhenko, N. Kolotova
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Abstract
(2-Oxo-2,3-dihydroimidazo[1,2-a]pyridin-3-yl)acetic acids (4a-c, 9a-c) were prepared from 2-aminopyridines by acylation with maleic or citraconic anhydrides and followed by Michael addition. Formation of 3-methyl substituted derivatives (9a-c) from citraconic anhydride was found to be regioselective. The molecular conformations of the products in the solution and in the crystal form were discussed based on 1 H NMR spectral and X-Ray data.
This study demonstrates the regioselective synthesis of (2-Oxo-2,3-dihydroimidazo[1,2-a]pyridin-3-yl)acetic acids from 2-aminopyridines using maleic or citraconic anhydrides and Michael addition, with
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