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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814511Generated: November 1, 2026

Imidazole → 1-(1-Imidazolyl)-3-(4-methoxyphenyl)isoquinoline hydrochloride

https://huagongshe.com/reaction/1814511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium hydrideHCID 24758—
Reactant1-Chloro-3-(4-methoxyphenyl)isoquinolineHCID 22502659—
SolventDimethylformamideHCID 6228—
Product1-(1-Imidazolyl)-3-(4-methoxyphenyl)isoquinoline hydrochlorideHCID 22503455—

Reaction Conditions

Temperature80 °C

Reaction Steps

1-Chloro-3-(4-methoxyphenyl)isoquinoline (405 mg) and imidazole (204 mg) were dissolved in N,N-dimethylformamide (5 ml), followed by the addition of 60% sodium hydride (60 mg), and the resulting mixture was stirred at 80° C. for 6 hr. The reaction mixture was partitioned between ethyl acetate and water. The resulting organic layer was washed with water, dried (over MgSO4) and evaporated. The resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), and then the resulting product was converted into a hydrochloride in a conventional manner, to give the hydrochloride of the title compound as a pale yellow amorphous (255 mg, yield; 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-6723cbde7b994c71aa53c70825652cae
Source noteuspto-grants-2005_04