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1H and 13C NMR identification of unexpected 3,4-dihydroquinoxalines in the syntheses of 1,5-benzodiazepine derivatives.

Magnetic resonance in chemistry : MRC (2005-04-30)
E M Tjiou, E G Lhoussaine, D Virieux, A Fruchier
RESUMEN

The reaction between o-phenylenediamines, dehydroacetic acid and aromatic aldehydes is shown to give not only the expected 1,5-benzodiazepine derivative but also a 3,4-dihydroquinoxaline, the structure of which was determined by its 1H and 13C 1D and 2D NMR spectra.

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Sigma-Aldrich
Dehydroacetic acid, ≥98.0% (T)