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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721734Generated: October 30, 2026

3-(Trifluoromethyl)benzoyl chloride → N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[3-(trifluoromethyl)benzoyl]thiourea

https://huagongshe.com/reaction/721734

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
Reactant4-(6,7-Dimethoxyquinazolin-4-yloxy)anilineHCID 11616363—
Reactant3-(trifluoromethyl)benzoyl isothiocyanateHCID 21784176—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product3-(trifluoromethyl)benzoyl isothiocyanateHCID 21784176—
ProductN-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[3-(trifluoromethyl)benzoyl]thioureaHCID 2189100785%

Reaction Steps

3-(Trifluoromethyl)-1-benzenecarbonyl isothiocyanate was prepared using commercially available 3-(trifluoromethyl)-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 3-(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 (75 mg, yield 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-d1c75313a51144afb0947d82c57b2a18
Source noteuspto-grants-2006_11