SYNTHESIS OF 1,2-DIHYDROINDOLO[1,7-AB][1,5]BENZODIAZEPINES AND RELATED STRUCTURES - NEW HETEROCYCLIC RING-SYSTEM

The synthesis of the novel 1,2‐dihydroindolo [1,7‐ab][1,5]benzodiazepine ring system 4 is described. Condensation of 2‐fluoronitrobenzene with indoline provided the starting material for the synthesis, 1‐(2‐nitrophenyl)indoline (1a) in high yield. The nitro group was reduced catalytically and the resulting amino function was acylated to afford the heterocycle percursor amide 3. Refluxing this amide in phosphorus oxychloride brought about a Bischler‐Napieralski type cyclodehydration to form the target 1,2‐dihydroindolo[1,7‐ab][1,5]benzodiazepine ring system. Dehydrogenation of the latter led to the fully aromatic indolo[1,7‐ab][1,5]benzodiazepine structure 5, while reduction with sodium borohydride provided the 1,2,6,7‐tetrahydroindolo[1,7‐ab]‐[1,5]benzodiazepine tetracycle 6. Copyright © 1979 Journal of Heterocyclic Chemistry