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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649152Generated: October 29, 2026

Ethanol → 7-Chloro-3-(1-imidazolylmethyl)-2-methylimidazo[2,1-a]isoquinoline

https://huagongshe.com/reaction/649152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantImidazoleHCID 795—
Reactant7-Chloro-2-methyl-3-trimethylammoniomethylimidazo[2,1-a]isoquinoline methylsulfateHCID 13821864—
SolventDimethyl SulfoxideHCID 679—
Product7-Chloro-3-(1-imidazolylmethyl)-2-methylimidazo[2,1-a]isoquinolineHCID 7041980641%

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethanol (50 ml) was added to a mixture of 7-chloro-2-methyl-3-trimethylammoniomethylimidazo[2,1-a]isoquinoline methylsulfate (2.3 g) and imidazole (0.95 g) in dimethyl sulfoxide (20 ml) and heated at 100° C. with stirring for 5 hours. After the removal of ethanol by distillation, the residue was poured into water. The resulting precipitates were collected by filtration, dried and recrystallized from ethyl acetate. The obtained crystals were chromatographed on silica gel (16 g) with a mixture of chloroform and methanol (10:1) as an eluent. The eluates were evaporated in vacuo and the residual solid was recrystallized from ethyl acetate to give 7-chloro-3-(1-imidazolylmethyl)-2-methylimidazo[2,1-a]isoquinoline (0.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04738967
Source datasetuspto-grants-1988_04
ORD IDord-d3fcd37c1fb04a1a9f81100b2f53b7e0
Source noteuspto-grants-1988_04