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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037840Generated: October 31, 2026

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

https://huagongshe.com/reaction/2037840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant2-Amino-5-bromopyridineHCID 70622—
SolventEthanolHCID 702—
ProductEthyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylateHCID 714193973%

Reaction Steps

15.00 g of 2-amino-5-bromopyridine (3), 16.99 g of ethyl 3-bromo-2-oxopropanoate were dissolved in ethanol (100 mL), and the solution is heated at reflux for 8 hours. The reaction mixture was concentrated, and saturated aqueous NaHCO3 was added to the residue. The resulting precipitate was isolated by filtration, and washed with water to afford 17.01 g of the titled compound as colorless powder (yield: 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575337B2
Source datasetuspto-grants-2013_11
ORD IDord-08cab82af9174561b4e0b03e9ac52327
Source noteuspto-grants-2013_11