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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871118Generated: October 26, 2026

N-bromobutanimide → 8-Acetoxy-3-bromo-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1871118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant8-Acetoxy-2-methylimidazo[1,2-a]pyridineHCID 18321926—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product8-Acetoxy-3-bromo-2-methylimidazo[1,2-a]pyridineHCID 1832187486.9%

Reaction Steps

To a solution of 8-acetoxy-2-methylimidazo[1,2-a]pyridine (100 mg) in ethanol (1 ml) was added N-bromosuccinimide (103 mg) under ice-cooling, and the mixture was stirred for 30 minutes at the same temperature. The mixture was diluted with ethyl acetate and washed with saturated sodium bicarbonate solution, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin layer chromatography (ethyl acetate) to give 8-acetoxy-3-bromo-2-methylimidazo[1,2-a]pyridine (123 mg) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100284
Source datasetuspto-grants-2000_08
ORD IDord-ab465fad7c0c4172b287edfb65c3b9e9
Source noteuspto-grants-2000_08