Synthesis of Ethyl 3‐phenylimidazo[1,2‐ <i>a</i> ]pyridine‐2‐carboxylate by Using 2‐Aminopyridines, Diethyl Oxalate, and Benzyl Bromides

A convenient new synthetic strategy was discovered for the synthesis of C3‐arylated imidazopyridines through alkylation of benzyl bromides with 2‐aminopyridines and base‐mediated condensation with diethyl oxalate. A series of C3‐arylated imidazopyridines was obtained in moderate to good yield. This protocol has the advantages of a mild reaction condition, broad substrate scope, and the absence of catalyst or additives.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-11-19
DOI
https://doi.org/10.1002/ejoc.202500958
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of Ethyl 3‐phenylimidazo[1,2‐ a ]pyridine‐2‐carboxylate by Using 2‐Aminopyridines, Diethyl Oxalate, and Benzyl Bromides

Sandeep Chandrashekharappa, Subrata Barick, Kaustav Dhara
European Journal of Organic Chemistry
Synthesis and Reactivity of Heterocycles
article

Synthesis of Ethyl 3‐phenylimidazo[1,2‐ a ]pyridine‐2‐carboxylate by Using 2‐Aminopyridines, Diethyl Oxalate, and Benzyl Bromides

Sandeep Chandrashekharappa, Subrata Barick, Kaustav Dhara
article en

Abstract

A convenient new synthetic strategy was discovered for the synthesis of C3‐arylated imidazopyridines through alkylation of benzyl bromides with 2‐aminopyridines and base‐mediated condensation with diethyl oxalate. A series of C3‐arylated imidazopyridines was obtained in moderate to good yield. This protocol has the advantages of a mild reaction condition, broad substrate scope, and the absence of catalyst or additives.

European Journal of Organic ChemistryVol. 28(48)
National Institute of Pharmaceutical Education and Research (IN)
National Institute of Pharmaceutical Education and Research, Raebareli
Openalex Percentile: Top 73%
Synthesis and Reactivity of Heterocycles
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