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Preparation of substituted piperazinones via tandem reductive amination-(N,N'-acyl transfer)-cyclization
Douglas C Beshore1, Christopher J Dinsmore
1Department of Medicinal Chemistry, Merck Research Laboratories, West Point, Pennsylvania 19486, USA. douglas_beshore@merck.com
Organic Letters
|April 2, 2002
Abstract:
[reaction: see text] A one-pot, tandem reductive amination-transamidation-cyclization reaction was employed to produce substituted piperazin-2-ones in good yields. Various amino acid methyl esters and transferable acyl groups were examined to establish the reaction's scope.