Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857211Generated: October 31, 2026

4-Chloro-6,7-dimethoxyquinoline → HCID 22132766, compound

https://huagongshe.com/reaction/1857211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
ReactantHCID 12299666HCID 12299666—
ReactantChloroform methanolHCID 21584188—
SolventDiglymeHCID 8150—
ProductHCID 22132766HCID 2213276633.1%

Reaction Conditions

Temperature160 °C

Reaction Steps

Under argon, 4-cyclohexylcarbonyl-1-hydroxybenzene (273 mg) obtained in Example 142 and 4-chloro-6,7-dimethoxyquinoline (100 mg) were dissolved in diethylene glycol dimethyl ether (0.2 ml), and the solution was refluxed at 160° C. for 30 minutes. The reaction mixture was partitioned between saturated aqueous sodium hydrogen carbonate and chloroform, and the chloroform layer was washed with brine and then dried with anhydrous magnesium sulfate. After removing the solvent by reduced-pressure distillation, the resulting residue was purified by chromatography on silica gel eluting with hexane/acetone and then with chloroform/methanol to obtain 58 mg of the title compound (yield: 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143764
Source datasetuspto-grants-2000_11
ORD IDord-dac9b0bb37bc4721b0b0270719c4f018
Source noteuspto-grants-2000_11