Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721869Generated: October 30, 2026

Toluene → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-methylphenyl}-N'-(2-fluorobenzoyl)thiourea

https://huagongshe.com/reaction/721869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-Fluorobenzoyl chlorideHCID 9808—
Reactant2-Fluorobenzoyl isothiocyanateHCID 15650508—
Reactant4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2-methylanilineHCID 21890510—
SolventEthanolHCID 702—
Product2-Fluorobenzoyl isothiocyanateHCID 15650508—
ProductN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-methylphenyl}-N'-(2-fluorobenzoyl)thioureaHCID 2189028352%

Reaction Steps

2-Fluoro-1-benzenecarbonyl isothiocyanate was prepared using commercially available 2-fluoro-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 2-Fluoro-1-benzenecarbonyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-methylaniline (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 (41 mg, yield 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-433ff339f75f4152a3705b5da99e287c
Source noteuspto-grants-2006_11