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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613618Generated: October 26, 2026

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

https://huagongshe.com/reaction/613618

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[l,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 numberUS06008229
Source datasetuspto-grants-1999_12
ORD IDord-f97c040479424b2abc671c7b18c9c9cf
Source noteuspto-grants-1999_12