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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721939Generated: October 29, 2026

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

https://huagongshe.com/reaction/721939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorobenzoyl chlorideHCID 74376—
Reactant4-(6,7-Dimethoxyquinazolin-4-yloxy)anilineHCID 11616363—
Reactant3-Fluorobenzoyl isothiocyanateHCID 14984172—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product3-Fluorobenzoyl isothiocyanateHCID 14984172—
ProductN-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-(3-fluorobenzoyl)thioureaHCID 2189029275%

Reaction Steps

3-Fluoro-1-benzenecarbonyl isothiocyanate was prepared using commercially available 3-fluoro-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-fluoro-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 (60 mg, yield 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-c865f1e659e7476f86882e45e0aa244a
Source noteuspto-grants-2006_11