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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788940Generated: October 30, 2026

3-Chloro-2,4-pentanedione → 3-Acetyl-7-chloro-2-methylimidazo[2,1-a]isoquinoline

https://huagongshe.com/reaction/1788940

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2,4-pentanedioneHCID 74328—
Reactant5-Chloroisoquinolin-1-amineHCID 13821825—
SolventChloroformHCID 6212—
Product3-Acetyl-7-chloro-2-methylimidazo[2,1-a]isoquinolineHCID 201424379%

Reaction Steps

To a suspension of 1-amino-5-chloroisoquinoline (10 g) in chloroform (150 ml) was added dropwise 3-chloro-2,4-pentanedione (11.3 g). The mixture was refluxed for 6 hours and then allowed to stand at room temperature over night. The mixture was washed successively with aqueous sodium bicarbonate and water, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (200 g) with chloroform as an eluent to afford a solid. This solid was recrystallized from ethyl acetate to give 3-acetyl-7-chloro-2-methylimidazo[2,1-a]isoquinoline (1.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686227
Source datasetuspto-grants-1987_08
ORD IDord-ede232d689f540df962a4f077637f4cb
Source noteuspto-grants-1987_08