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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788938Generated: November 4, 2026

Acetic Anhydride → 3-Acetoxymethyl-7-chloro-2-methylimidazo[2,1-a]isoquinoline

https://huagongshe.com/reaction/1788938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant7-Chloro-3-hydroxymethyl-2-methylimidazo[2,1-a]isoquinolineHCID 13821860—
SolventPyridineHCID 1049—
Product3-Acetoxymethyl-7-chloro-2-methylimidazo[2,1-a]isoquinolineHCID 1382186135.8%

Reaction Steps

Acetic anhydride (0.71 g) was added dropwise to a suspension of 7-chloro-3-hydroxymethyl-2-methylimidazo[2,1-a]isoquinoline (1.43 g) in pyridine (14 ml) and the mixture was stirred at room temperature for 24 hours. The mixture was evaporated in vacuo and the residue was extracted with chloroform after an addition of water to it. The extract was washed with water, dried over magnesium sulfate, treated with activated charcoal and evaporated in vacuo. The crystalline residue was recrystallized from a mixture of ethyl acetate and diisopropyl ether to give 3-acetoxymethyl-7-chloro-2-methylimidazo[2,1-a]isoquinoline (0.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686227
Source datasetuspto-grants-1987_08
ORD IDord-1dc58f9bdebb49a9ac8f93e49b2889db
Source noteuspto-grants-1987_08