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Expedient Synthesis of 6-Aryl Derivatives of 3,4-Dihydro-1,4,4a,6a-tetraaza-benzo[a]fluoren-2-one: A New Heterocyclic Framework.

Authors :
Reddy, GadeSrinivas
Rajasekhar, Kadaboina
Praveen, Cherukupally
Mukkanti, Kaga
Reddy, PadiPratap
Source :
Synthetic Communications. 2008, Vol. 38 Issue 22, p3884-3893. 10p. 1 Diagram, 2 Charts.
Publication Year :
2008

Abstract

3,4-Dihydro-1,4,4a,6a-tetraaza-benzo[a]fluoren-2-one, a new tetracyclic heterocyclic framework, is designed through a simple and convenient synthetic sequence. Its 6-aryl derivatives are synthesized starting from 1H-indole-2-carboxylic acid. The reaction of differently substituted phenacyl bromides with 1H-indole-2-carboxylic acid and POCl3-mediated cyclization of the resultant 1H-indole-2-carboxylic acid phenacyl ester provided 2-oxa-4a-aza-fluoren-1-one, and its sequential reaction with hydrazine and 2-chloro-acetamide furnished the desired new heterocyclic compounds 7a-f. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00397911
Volume :
38
Issue :
22
Database :
Academic Search Index
Journal :
Synthetic Communications
Publication Type :
Academic Journal
Accession number :
34870817
Full Text :
https://doi.org/10.1080/00397910802238742