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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228640Generated: October 29, 2026

Bromosalicylchloranilide → HCID 57756539, compound

https://huagongshe.com/reaction/228640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromosalicylchloranilideHCID 77254—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 57756539HCID 5775653925.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

4-Chloro-6,7-dimethoxyquinoline (100 mg), 5-bromo-4′-chlorosalicylanilide (653 mg), and 4-dimethylaminopyridine (244 mg) were suspended in o-dichlorobenzene (1 ml), and the suspension was stirred at 120° C. overnight. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-hexane to give the title compound (59 mg, yield 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-490f7a0df62946948cde51cb5fbc5628
Source noteuspto-grants-2009_07