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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721750Generated: October 30, 2026

4-Bromobenzoyl chloride → N-(4-Bromobenzoyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-3-fluorophenyl}thiourea

https://huagongshe.com/reaction/721750

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzoyl chlorideHCID 68515—
Reactant4-bromobenzoyl isothiocyanateHCID 244995—
Reactant4-((6,7-Dimethoxyquinolin-4-yl)oxy)-3-fluorobenzenamineHCID 11426997—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product4-bromobenzoyl isothiocyanateHCID 244995—
ProductN-(4-Bromobenzoyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-3-fluorophenyl}thioureaHCID 2188991691%

Reaction Steps

4-Bromo-1-benzenecarbonyl isothiocyanate was prepared using commercially available 4-bromo-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-3-fluoroaniline (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 4-bromo-1-benzenecarbonyl isothiocyanate in ethanol (1 ml) was then added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (81 mg, yield 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-6b84ad7d513f4ff0ab2c3b77c2bb5473
Source noteuspto-grants-2006_11