Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721933Generated: October 29, 2026

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

https://huagongshe.com/reaction/721933

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichlorobenzoyl chlorideHCID 76191—
Reactant4-(6,7-Dimethoxyquinazolin-4-yloxy)anilineHCID 11616363—
ReactantHCID 16774862HCID 16774862—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 16774862HCID 16774862—
ProductN-(3,5-Dichlorobenzoyl)-N'-{4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}thioureaHCID 2189066045%

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. 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 3,5-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 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-ec548bd942c94ccf99369c65e78e6b78
Source noteuspto-grants-2006_11