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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721934Generated: October 30, 2026

3,5-Dichlorobenzoyl chloride → N-{2-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3,5-dichlorobenzoyl)thiourea

https://huagongshe.com/reaction/721934

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichlorobenzoyl chlorideHCID 76191—
Reactant4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-chloroanilineHCID 11221223—
ReactantHCID 16774862HCID 16774862—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 16774862HCID 16774862—
ProductN-{2-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3,5-dichlorobenzoyl)thioureaHCID 2189103647%

Reaction Steps

3,5-Dichloro-1-benzenecarbonyl isothiocyanate was prepared using commercially available 3,5-dichloro-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 2-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 3,5-dichloro-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 (40 mg, yield 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-45fdf49099a64cf1a5fd04e6a8323b7e
Source noteuspto-grants-2006_11