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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721863Generated: October 29, 2026

Toluene → N-(2,4-Difluorobenzoyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,3-dimethylphenyl}thiourea

https://huagongshe.com/reaction/721863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2,4-Difluorobenzoyl chlorideHCID 588081—
Reactant2,4-Difluorobenzoyl isothiocyanateHCID 13715284—
Reactant4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylanilineHCID 21890439—
SolventEthanolHCID 702—
Product2,4-Difluorobenzoyl isothiocyanateHCID 13715284—
ProductN-(2,4-Difluorobenzoyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,3-dimethylphenyl}thioureaHCID 2189015074%

Reaction Steps

2,4-Difluoro-1-benzenecarbonyl isothiocyanate was prepared using commercially available 2,4-difluoro-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 2,4-Difluoro-1-benzenecarbonyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylaniline (50 mg), toluene (5 ml), and ethanol (1 ml) were 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 (60 mg, yield 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-e12f88090e65428daca17a84962573bb
Source noteuspto-grants-2006_11