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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721780Generated: October 26, 2026

2,5-Dimethylbenzoic acid → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2,5-dimethylbenzoyl)thiourea

https://huagongshe.com/reaction/721780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dimethylbenzoic acidHCID 11892—
ReactantThionyl ChlorideHCID 24386—
Reactant4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
Reactant2,5-Dimethylbenzoyl chlorideHCID 12351885—
Reactant2,5-Dimethyl-1-benzenecarbonyl isothiocyanateHCID 21890996—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(2,5-dimethylbenzoyl)thioureaHCID 2189065891%

Reaction Conditions

Temperature100 °C

Reaction Steps

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 2,5-dimethylbenzoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 2,5-dimethyl-1-benzenecarbonyl isothiocyanate was prepared using the resultant 2,5-dimethyl-1-benzenecarbonyl chloride as a starting compound according to the description of the literature. 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 2,5-dimethyl-1-benzenecarbonyl isothiocyanate in ethanol (1 ml) was 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 (75 mg, yield 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-2d14b514439e41238dce0d9920696bd5
Source noteuspto-grants-2006_11