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Some nucleophilic substitutions in 2-cyano-3-nitroimidazo[1,2-a]pyridine

✍ Scribed by Lucina Arias; Héactor Salgado-Zamora; Elena Campos; Alicia Reyes; Humberto Cervantes; Edward C. Taylor


Publisher
Journal of Heterocyclic Chemistry
Year
2006
Tongue
English
Weight
296 KB
Volume
43
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

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In some nucleophilic substitution reactions of 2‐cyano‐3‐nitroimidazo[1,2‐a]pyridine, nitrogen (alkylamines, guanidine) and oxygen nucleophiles (alkoxides) underwent substitution of the 2‐cyano group, while sulfur nucleophiles (alkylthiols) underwent substitution of the 3‐nitro group.


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## Abstract Previously unknown 3‐fluoro‐2‐trifluoromethylimidazo[1,2‐a]pyridines (IV) are synthesized via cyclization of readily available imines (III).