Selective C-acylation of 2-aminoimidazo[1,2- a ]pyridine: Application to the synthesis of imidazopyridine-fused [1,3]diazepinones

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Abstract

A series of 20 optically pure 3,4-dihydro-5H-pyrido[1′,2′:1,2] imidazo[4,5-d][1,3]diazepin-5-ones which form a new family of azaheterocycle-fused [1,3]diazepines were synthesized in four steps with 17-66% overall yields. The key step consists of a selective C-acylation reaction of easily accessible 2-aminoimidazo[1,2-a]pyridine at C-3. © 2012 American Chemical Society.

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Masurier, N., Aruta, R., Gaumet, V., Denoyelle, S., Moreau, E., Lisowski, V., … Maillard, L. T. (2012). Selective C-acylation of 2-aminoimidazo[1,2- a ]pyridine: Application to the synthesis of imidazopyridine-fused [1,3]diazepinones. Journal of Organic Chemistry, 77(7), 3679–3685. https://doi.org/10.1021/jo300364d

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