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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349748Generated: October 30, 2026

Ethyl bromopyruvate → Ethyl 6-fluoroimidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/349748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
SolventDiethyl EtherHCID 3283—
ProductEthyl 6-fluoroimidazo[1,2-a]pyridine-2-carboxylateHCID 40148106—

Reaction Steps

To a solution of 2-amino-5-fluoropyridine (1.12 g) in diethyl ether (25 ml) was added ethyl bromopyruvate (1.25 ml). the mixture was stirred for 1 hour. The resultant solid was filtered off, suspended in ethanol and heated at reflux for 4 hours. The solvent was removed by evaporation and the residue partitioned between ethyl acetate (100 ml) and aqueous sodium bicarbonate solution (100 ml). The organic layer was separated, dried, (magnesium sulfate) and the solvent removed by evaporation. The residue was purified by flash chromatography (silica) eluting with ethyl acetate:hexane (3:1) to give the sub-title compound as a colourless solid (1.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179922B2
Source datasetuspto-grants-2007_02
ORD IDord-4dd1b4c92530425f8f6e2a44d2029e20
Source noteuspto-grants-2007_02