Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You or Your Team.

Learn More →

An aminoimidazole and its utility in heterocyclic synthesis

An aminoimidazole and its utility in heterocyclic synthesis Aminoacetonitrile (1) reacted with acetamidinium chloride to give 4‐aminoimidazole (4), which reacted with DMFDMA to yield imidazole derivative 7 and with benzylidinemalononitrile and ethoxymethylene malononitrile to give imidazo(1,5‐a)pyrimidine derivatives 12 and 15. Compound 1 reacted with β‐crotononitrile to yield pyridine derivative 20. Imidazo(1,2‐a)pyridine derivative 23 could be obtained via the reaction of 20 with DMFDMA. © 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:503–508, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10178 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

An aminoimidazole and its utility in heterocyclic synthesis

Heteroatom Chemistry , Volume 14 (6) – Jan 1, 2003

Loading next page...
 
/lp/wiley/an-aminoimidazole-and-its-utility-in-heterocyclic-synthesis-kX6owWwt1L

References (21)

Publisher
Wiley
Copyright
Copyright © 2003 Wiley Periodicals, Inc.
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/hc.10178
Publisher site
See Article on Publisher Site

Abstract

Aminoacetonitrile (1) reacted with acetamidinium chloride to give 4‐aminoimidazole (4), which reacted with DMFDMA to yield imidazole derivative 7 and with benzylidinemalononitrile and ethoxymethylene malononitrile to give imidazo(1,5‐a)pyrimidine derivatives 12 and 15. Compound 1 reacted with β‐crotononitrile to yield pyridine derivative 20. Imidazo(1,2‐a)pyridine derivative 23 could be obtained via the reaction of 20 with DMFDMA. © 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:503–508, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10178

Journal

Heteroatom ChemistryWiley

Published: Jan 1, 2003

There are no references for this article.