Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334548Generated: October 25, 2026

2-Aminopyridine → Ethyl imidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/334548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantEthyl bromopyruvateHCID 66144—
SolventEthanolHCID 702—
ProductEthyl imidazo[1,2-a]pyridine-2-carboxylateHCID 81880762.8%

Reaction Steps

A solution of 2-amino-pyridine (2 g, 21 mmol) and ethyl bromopyruvate (4.14 g, 21 mmol) in ethanol (31 mL) was stirred under reflux for 24 h. The solvent was evaporated, and the residue was dissolved in a minimum volume of water. The solution was neutralized (pH=8) with saturated NaHCO3. The aqueous layer was extracted with AcOEt and the organic layer was washed with saturated NaCl. The solvent was removed under pressure to afford 2.51 g of ethyl imidazo[1,2-a]pyridine-2-carboxylate (Yield: 62%) as an orange oil which can be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-365fa8e003334baa88f3d985f4ade44a
Source noteuspto-grants-2014_11