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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721768Generated: October 31, 2026

4-Ethoxybenzoyl Chloride → N-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(4-ethoxybenzoyl)thiourea

https://huagongshe.com/reaction/721768

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Ethoxybenzoyl ChlorideHCID 140059—
Reactant3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]anilineHCID 11739027—
ReactantHCID 21891013HCID 21891013—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductN-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(4-ethoxybenzoyl)thioureaHCID 2189072389%
ProductHCID 21891013HCID 21891013—

Reaction Steps

4-Ethoxy-1-benzenecarbonyl isothiocyanate was prepared using commercially available 4-ethoxy-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 4-ethoxy-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 (72 mg, yield 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-14ca27b69a3e4e60ae4a292887647a0f
Source noteuspto-grants-2006_11