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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721915Generated: October 25, 2026

Thionyl Chloride → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethyl-N'-[3-(2-methoxyphenyl)propanoyl]thiourea

https://huagongshe.com/reaction/721915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-(o-Methoxyphenyl)propionic acidHCID 80652—
Reactant4-Phenylbutanoyl ChlorideHCID 11789865—
Reactant3-(2-Methoxyphenyl)propanoyl isothiocyanateHCID 21890064—
ReactantN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethylamineHCID 21891226—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethyl-N'-[3-(2-methoxyphenyl)propanoyl]thioureaHCID 2189105752%

Reaction Conditions

Temperature100 °C

Reaction Steps

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 3-(2-methoxyphenyl)propanoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 3-(2-methoxyphenyl)propanoyl isothiocyanate was prepared using the resultant 4-phenylbutanoyl chloride as a starting compound according to the description of the literature. N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethylamine (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 3-(2-methoxyphenyl)propanoyl 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 (44 mg, yield 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-0b8a5a599c614390bb76d4da292ab919
Source noteuspto-grants-2006_11