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A Facile Three-Steps, One-Pot Synthesis of Novel 2-Alkylamino and 2-Dialkylamino-4H-Pyrido [1, 2-A][1,3,5] Triazin-4-Ones from 2-Aminopyridine and 2-Aminopicolines

Authors: Dagdag, Said; Belbahloul, Mounir; Anouar, Mohamed; Kopp, Maria; Anouar, Abdellah; Hmyene, Mohamed;

A Facile Three-Steps, One-Pot Synthesis of Novel 2-Alkylamino and 2-Dialkylamino-4H-Pyrido [1, 2-A][1,3,5] Triazin-4-Ones from 2-Aminopyridine and 2-Aminopicolines

Abstract

Abstract : A straightforward approach to novel 2-dialkylamino-4H-pyrido[1,2-a][1,3,5]triazin-4-ones synthesis is presented. The construction of these compounds was achieved by one-pot synthesis involving condensation of 2-aminopyridine or 2-aminopicolines with ethoxycarbonylisothiocianate, followed by amination of the thioureas, and finally thermal ring closure of resulting guanidines. This allowed access to the unreported title heterocycles. We described an efficient, facile, one-pot synthesis of a novel 2-dialkylamino-4H-pyrido[1,2-a][1,3,5]triazin-4-ones in order to obtain a library of pyridotriazines which will be used as building blocks in medicinal chemistry.

Keywords

Heterocycles, Infrared and Masse Spectroscopy, NMR spectroscopy, pyridotriazines, Synthesis.

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This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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