ChemInform Abstract: Synthesis of Pyrrolo[3,4‐e][1,4]diazepine Derivatives. Part l. 2,3‐Dihydro‐5‐aryl‐7‐aryl‐pyrrolo[3,4‐e][1,4]diazepine‐6‐thioxo‐8‐(lH,7H)‐ones.
“…A modification of the above route,53 leading to 1,4-diazepine derivatives 52, consisted in the formation of pyrrolidine derivatives by cyclocondensation between Schiff bases 59 of ethylenediamine (61) or aryl-3-oxo thioanilides and oxalyl chloride. The so obtained compounds 60 Scheme 18underwent intramolecular cyclization in alkaline medium to afford fused pyrrolo[3,4-e]-1,4-diazepines 52 (Scheme 19).54,55,59 All compounds of this series are of interest because of their potential biological activity. One of the sulfur analogs, 6-thioxopyrrolo[3,4-e]-1,4-diazepine, exhibits particularly strong analgesic and anti-inflammatory activity 57.…”
This review article, covering the literature from 1891 to 1999, deals with the methods of preparation of pyrrolidinetrione derivatives, emphasis being placed on methods of reasonable efficiency. A general applicability of these compounds as versatile building blocks in synthesis of fused heterocyclic systems is in focus. Pyrrolidine-2,3,4-trione Derivatives in the Synthesis of Anellated Nitrogen-Containing 5,5-Ring Systems 4 Hydrogenation of Pyrrolidine-2,3,5-triones 5 Su mmary
“…A modification of the above route,53 leading to 1,4-diazepine derivatives 52, consisted in the formation of pyrrolidine derivatives by cyclocondensation between Schiff bases 59 of ethylenediamine (61) or aryl-3-oxo thioanilides and oxalyl chloride. The so obtained compounds 60 Scheme 18underwent intramolecular cyclization in alkaline medium to afford fused pyrrolo[3,4-e]-1,4-diazepines 52 (Scheme 19).54,55,59 All compounds of this series are of interest because of their potential biological activity. One of the sulfur analogs, 6-thioxopyrrolo[3,4-e]-1,4-diazepine, exhibits particularly strong analgesic and anti-inflammatory activity 57.…”
This review article, covering the literature from 1891 to 1999, deals with the methods of preparation of pyrrolidinetrione derivatives, emphasis being placed on methods of reasonable efficiency. A general applicability of these compounds as versatile building blocks in synthesis of fused heterocyclic systems is in focus. Pyrrolidine-2,3,4-trione Derivatives in the Synthesis of Anellated Nitrogen-Containing 5,5-Ring Systems 4 Hydrogenation of Pyrrolidine-2,3,5-triones 5 Su mmary
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