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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699184Generated: October 26, 2026

Pyridine → 8-Acetoxy-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1699184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Methylimidazo[1,2-a]pyridin-8-olHCID 820953—
SolventDichloromethaneHCID 6344—
Product8-Acetoxy-2-methylimidazo[1,2-a]pyridineHCID 18321926102%

Reaction Steps

A mixture of 8-hydroxy-2-methylimidazo[1,2-a]pyridine (10 g), acetic anhydride (10.3 g) and pyridine (10.7 g) in anhydrous dichloromethane (100 ml) was stirred for 1 hour at ambient temperature and allowed to stand overnight. The mixture was washed with water, and the organic layer was separated. The aqueous layer was neutralized with sodium bicarbonate and extracted with chloroform. The combined organic layers were washed with saturated sodium bicarbonate solution, dried over magnesium sulfate and evaporated in vacuo to give 8-acetoxy-2-methylimidazo[1,2-a]pyridine (13.1 g) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344462B1
Source datasetuspto-grants-2002_02
ORD IDord-9a7b640f5bd64282a9a78867344fc1f9
Source noteuspto-grants-2002_02