Synthesis of 3-Amino-1,5-benzodiazepine-2-one Derivatives from Dehydroalanine Derivatives

Abstract

A convenient method was developed for synthesizing 3-amino-1,5-benzodiazepine-2-one derivatives via a Michael addition reaction of o-phenylenediamine with dehydroalanine HFI or HOBt ester derivatives (HFI = 1,1,1,3,3,3-hexafluoro-2-propyl; HOBt = 1,2,3-benzotriazol-1-ol monohydrate), followed by cyclization. Interestingly, the regio- and diastereoselectivities were confirmed by comparing the HFI and HOBt esters. These simple methods were used to synthesize various N-substituted 3-amino-1,5-benzodiazepine-2-one derivatives in good yields.

Key words

1,5-benzodiazepines - Michael additions - o-phenylenediamine - dehydroalanine - intramolecular cyclization

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