Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721896Generated: October 30, 2026

2,4-Dimethoxybenzoyl chloride → N-(2,4-Dimethoxybenzoyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2-fluorophenyl}thiourea

https://huagongshe.com/reaction/721896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dimethoxybenzoyl chlorideHCID 2734719—
Reactant4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-fluoroanilineHCID 11301470—
ReactantHCID 21890675HCID 21890675—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductN-(2,4-Dimethoxybenzoyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2-fluorophenyl}thioureaHCID 2189028767%
ProductHCID 21890675HCID 21890675—

Reaction Steps

2,4-Dimethoxy-1-benzenecarbonyl isothiocyanate was prepared using commercially available 2,4-dimethoxy-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-fluoroaniline (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 2,4-dimethoxy-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 (54 mg, yield 67%). Mass spectrometry value (ESI-MS, m/z): 538 (M++1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-b23d6cd3bfe9440e90b42f35bb535f57
Source noteuspto-grants-2006_11