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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613489Generated: October 26, 2026

Imidazole → 8-(2,6-Dichlorobenzoylamino)-3-(imidazol-1-ylmethyl)quinoline

https://huagongshe.com/reaction/613489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantN-bromobutanimideHCID 67184—
Reactant2,2'-Azobis(2,4-dimethyl-4-methoxyvaleronitrile)HCID 85867—
Reactant3-Bromomethyl-8-(2,6-dichlorobenzoylamino)quinolineHCID 19592388—
Reactant8-(2,6-Dichlorobenzoylamino)-3-methylquinolineHCID 19592707—
Solvent1,2-DichloroethaneHCID 11—
SolventCarbon TetrachlorideHCID 5943—
Product8-(2,6-Dichlorobenzoylamino)-3-(imidazol-1-ylmethyl)quinolineHCID 19592660—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 8-(2,6-dichlorobenzoylamino)-3-methylquinoline (104 mg), N-bromosuccinimide (67.1 mg) and 2,2'-azobis(2,4-dimethyl-4-methoxyvaleronitrile) (20.1 mg) in carbon tetrachloride (3 ml) was refluxed for 2 hours. After cooling, the mixture was washed with water, saturated sodium bicarbonate solution and brine, dried over magnesium sulfate and evaporated in vacuo to give a residue containing 3-bromomethyl-8-(2,6-dichlorobenzoylamino)quinoline. The residue was dissolved in ethylene chloride, and imidazole (64.1 mg) was added thereto. After stirring for 2.5 hours at 60° C., the mixture was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (ethyl acetate-dichloromethane) to give 8-(2,6-dichlorobenzoylamino)-3-(imidazol-1-ylmethyl)quinoline (36.2 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008230
Source datasetuspto-grants-1999_12
ORD IDord-08c53389d8a24d998fde806acea60354
Source noteuspto-grants-1999_12