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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467823Generated: October 25, 2026

Ethyl bromopyruvate → Ethyl 8-bromo-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/467823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant3-Bromo-5-(trifluoromethyl)pyridin-2-amineHCID 13064155—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductEthyl 8-bromo-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylateHCID 8666472178.9%

Reaction Steps

To a solution of 2-amino-3-bromo-5-(trifluoromethyl)pyridine (10.0 g, 41.5 mmol) in 1,2 dimethoxyethane (300 mL) at room temperature was added ethyl bromopyruvate (9.889 g, 45.64 mmol) dropwise. The reaction mixture was heated to reflux for 18 h. The 1,2-dimethoxyethane was removed under reduced pressure and the residual solid was recrystallized from 1-chlorobutane. The solid was isolated by filtration and dried to afford an off-white solid, 8-bromo-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid, ethyl ester (11.044 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623890B2
Source datasetuspto-grants-2014_01
ORD IDord-0b7f42c6d6d5439da1e9827d5f87c50a
Source noteuspto-grants-2014_01