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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497857Generated: October 31, 2026

Sulfuric Acid → Ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/1497857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantEthyl 2-chloro-3-hydroxyacrylate potassium saltHCID 86677443—
SolventEthanolHCID 702—
ProductEthyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 22031055—

Reaction Conditions

Temperature78 °C

Reaction Steps

To a stirring suspension of 5-bromopyridin-2-amine (1.2 g, 7.05 mmol) and ethyl 2-chloro-3-hydroxyacrylate potassium salt (6.6 g, 28.19 mmol) (prepared in a similar manner as 22) in EtOH (100 mL) at room temperature was added sulfuric acid (751 L, 14.10 mmol) dropwise. The reaction mixture was heated at 78° C. overnight. The reaction was cooled to room temperature and the solvent was concentrated. The residue was taken in water and the pH was adjusted between 6-8 with saturated sodium bicarbonate. The crude product was extracted with ethyl acetate. The organic was washed with brine and dried over anhydrous sodium sulfate. The crude product was purified by silica chromatography to yield ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate (24s). MS m/z 270.2 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199981B2
Source datasetuspto-grants-2015_12
ORD IDord-7666b4a41a024df381e0edef1a0c6dd6
Source noteuspto-grants-2015_12