Synthesis of new 2-chloro-4-(3-aryl-2,4-diphenyl-3h-triazolidine-5-on- 1-yl)quinoline-3-carbonitriles by a cycloaddition route using carbodiimides and nitrones. A novel thermal decomposition to 4-aminoquinolines

Article abstract of DOI:10.1080/00397919808004913

A convenient synthesis of the triazolidinones-1-yl derivatives 7 via cycloaddition reactions and their thermolysis to afford 4-amino-2- chloroquinline-3-carbonitrile 10 is reported.

Full text of DOI:10.1080/00397919808004913

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Synthetic Communications:
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Synthetic Organic Chemistry
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Synthesis of New 2-Chloro-4-
(3-Aryl-2,4-Diphenyl-3H-
Triazolidine-5-on-1-
yl)Quinoline-3-Carbonitriles
by a Cyclo-Addition Route
Using Carbodiimides and
Nitrones. A Novel Thermal
Decomposition to 4-
Aminoquinolines
Ramadan AhmedMekheimer a
a Chemistry Department, Faculty of Science, El-
Minia University, 61519, El-Minia, A. R. Egypt
Version of record first published: 22 Aug 2006.
To cite this article: Ramadan AhmedMekheimer (1998): Synthesis of New 2-
Chloro-4-(3-Aryl-2,4-Diphenyl-3H-Triazolidine-5-on-1-yl)Quinoline-3-Carbonitriles
by a Cyclo-Addition Route Using Carbodiimides and Nitrones. A Novel Thermal
Decomposition to 4-Aminoquinolines, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 28:19,
3665-3674
To link to this article: http://dx.doi.org/10.1080/00397919808004913

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