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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772033Generated: November 1, 2026

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

https://huagongshe.com/reaction/1772033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantEthyl bromopyruvateHCID 66144—
SolventTetrahydrofuranHCID 8028—
ProductEthyl imidazo[1,2-a]pyridine-2-carboxylateHCID 81880760.3%

Reaction Steps

A solution of 2-aminopyridine (5.0 g, 53.2 mmol) in THF (150 mL) was treated with ethyl bromopyruvate (10.32 g, 57.0 mmol) at room temperature followed by heating the mixture at reflux for 16 h. The resulting white precipitate was collected by Filtration and washed with THF (10 mL). Recrystallization of the solids from boiling EtOH (20 mL) gave ethyl imidazo[1,2-a]pyridine-2-carboxylate (6.10 g, 60% yield). ESI MS: m/z 191 [M+1]+. See, e.g., J. Med. Chem., 2003, 46, 3914-29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249162B2
Source datasetuspto-grants-2016_02
ORD IDord-87fb08b070ce4000aa0c90363e3cacba
Source noteuspto-grants-2016_02