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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474172Generated: November 2, 2026

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

https://huagongshe.com/reaction/1474172

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 numberUS09018228B2
Source datasetuspto-grants-2015_04
ORD IDord-6a03ad3f088f4e9fb9a07b0efd2649e4
Source noteuspto-grants-2015_04