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.
Authors
- Sandeep Chandrashekharappa (ORCID: https://orcid.org/0000-0003-2475-7270)
- Subrata Barick
- Kaustav Dhara
Institutions
- National Institute of Pharmaceutical Education and Research (IN)
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
Funders
- National Institute of Pharmaceutical Education and Research, Raebareli