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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721961Generated: October 26, 2026

p-Octylbenzoic acid → N-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(4-octylbenzoyl)thiourea

https://huagongshe.com/reaction/721961

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Octylbenzoic acidHCID 19147—
ReactantThionyl ChlorideHCID 24386—
ReactantBenzoyl chloride, 4-octyl-HCID 170865—
Reactant3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]anilineHCID 11739027—
Reactant4-Octyl-1-benzenecarbonyl isothiocyanateHCID 21890973—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductN-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(4-octylbenzoyl)thioureaHCID 2189081858%

Reaction Conditions

Temperature100 °C

Reaction Steps

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 4-octylbenzoic acid (40 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 4-octyl-1-benzenecarbonyl isothiocyanate was prepared using the resultant 4-octyl-1-benzenecarbonyl chloride 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-octyl-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 (53 mg, yield 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-f733f7bfb067432b870060d7f83b7889
Source noteuspto-grants-2006_11