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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721682Generated: October 29, 2026

2-(Trifluoromethyl)benzoyl chloride → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-phenyl}-N'-[2-(trifluoromethyl)benzoyl]thiourea

https://huagongshe.com/reaction/721682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
Reactant4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
ReactantHCID 16776691HCID 16776691—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 16776691HCID 16776691—
ProductN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-phenyl}-N'-[2-(trifluoromethyl)benzoyl]thioureaHCID 2188999895%

Reaction Steps

2-(Trifluoromethyl)-1-benzenecarbonyl isothiocyanate was prepared using commercially available 2-(trifluoromethyl)-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 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-(trifluoromethyl)-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 (83 mg, yield 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-57396457530c485b9d0d911cf70d62e4
Source noteuspto-grants-2006_11