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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721702Generated: October 30, 2026

2-Bromobenzoyl chloride → N-(2-Bromobenzoyl)-N'-{3-chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}thiourea

https://huagongshe.com/reaction/721702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzoyl chlorideHCID 23542—
Reactant3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]anilineHCID 11739027—
Reactant2-Bromobenzoyl isothiocyanateHCID 13362324—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product2-Bromobenzoyl isothiocyanateHCID 13362324—
ProductN-(2-Bromobenzoyl)-N'-{3-chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}thioureaHCID 2189079070%

Reaction Steps

2-Bromo-1-benzenecarbonyl isothiocyanate was prepared using commercially available 2-bromo-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]aniline (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 2-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 (61 mg, yield 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-2d36fedb04a14702980777823603b3f2
Source noteuspto-grants-2006_11