Synthesis of Linear Azolo and Pyrido Quinolines from Quinoline Derivatives

Author(s): Paola Corona, Sandra Piras, Michele Palomba, Antonio Carta

Journal Name: Mini-Reviews in Organic Chemistry

Volume 5 , Issue 4 , 2008


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Abstract:

Angular N-tricyclic systems as triazolo[4,5-f]quinolines, triazolo[4,5-h]quinolines, imidazo[4,5-f]quinolines, imidazo[4,5- h]quinolines were in the past obtained by connection of either f or h sides of the quinoline ring and both the adjacent carbon atoms of five-membered rings containing nitrogen atoms. Several attempts at obtaining the corresponding linear N-tricycles were made in the last century, but only the angular derivatives were obtained. Since 2000 a new simple pathway, involving suitable quinoline derivatives, which afforded the linear azolo and pyrido quinolines (imidazo[4,5-g]quinolines, triazolo[4,5-g]quinolines and pyrido[2,3- g]quinoxalines) has been developed. Several linear N-tricyclic derivatives have shown some interesting pharmaceutical activity.

Keywords: Imidazo[4,5-g]quinolines, triazolo[4,5-g]quinolines, pyrido[2,3-g]quinoxalines, aminoquinolines, antitubercular activity, antifungal activity, anticancer activity, antiviral activity

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Article Details

VOLUME: 5
ISSUE: 4
Year: 2008
Page: [295 - 302]
Pages: 8
DOI: 10.2174/157019308786242197
Price: $65

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