Research on nitrogen and sulfur heterocyclic compounds: Synthesis of 10H‐pyrrolo[1,2‐a]thieno[3,4‐e][1,4]‐diazepin‐5(4H)‐one and some derivatives
Identifieur interne : 001459 ( France/Analysis ); précédent : 001458; suivant : 001460Research on nitrogen and sulfur heterocyclic compounds: Synthesis of 10H‐pyrrolo[1,2‐a]thieno[3,4‐e][1,4]‐diazepin‐5(4H)‐one and some derivatives
Auteurs : Abdelali Daich [France] ; Jean Morel [France] ; Bernard Decroix [France]Source :
- Journal of Heterocyclic Chemistry [ 0022-152X ] ; 1994-03.
Abstract
The synthesis of 10H‐pyrrolo[1,2‐a]thieno[3,4‐e][1,4]diazepin‐5(4H)‐one (16) and some derivatives are described from methyl 3‐bromomethylthiophene‐4‐carboxylate (5). The key step of these sequences is the intramolecular cyclization of the carbonylazides 12 and 13.
Url:
DOI: 10.1002/jhet.5570310214
Affiliations:
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ISTEX:4A2BA0EDC5F6EFFB50D8D69A8C50092DD9E9A77ELe document en format XML
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ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract">The synthesis of 10H‐pyrrolo[1,2‐a]thieno[3,4‐e][1,4]diazepin‐5(4H)‐one (16) and some derivatives are described from methyl 3‐bromomethylthiophene‐4‐carboxylate (5). 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