Quinazolines and 1,4-benzodiazepines. Part XXXII. The acetic anhydride rearrangement of 1,4-benzodiazepinones to isoindoles
Abstract
1,3-Dihydro-5-phenyl-2H-1,4-benzodiazepin-2-ones unsubstituted in the 1-position rearrange to 1-acetyliso-indoles in the presence of acetic anhydride and pyridine. The structure of the rearranged products has been established by alternative syntheses, and the mechanism of the rearrangement is discussed.
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