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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613617Generated: October 25, 2026

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

https://huagongshe.com/reaction/613617

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 30 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 numberUS06008229
Source datasetuspto-grants-1999_12
ORD IDord-c73c14e2cff948938980e69f1e0397eb
Source noteuspto-grants-1999_12