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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721902Erstellt: 25. Oktober 2026

3,5-Dimethylbenzoic acid → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-phenyl}-N'-(3,5-dimethylbenzoyl)thiourea

https://huagongshe.com/reaction/721902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-Dimethylbenzoic acidHCID 10356—
EduktThionyl ChlorideHCID 24386—
Edukt3,5-Dimethylbenzoyl ChlorideHCID 81088—
Edukt4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
Edukt3,5-Dimethyl-1-benzenecarbonyl isothiocyanateHCID 16775643—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
ProduktN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-phenyl}-N'-(3,5-dimethylbenzoyl)thioureaHCID 2189001847%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Toluene (20 ml) and thionyl chloride (1 ml) was added to commercially available 3,5-dimethylbenzoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 3,5-dimethyl-1-benzenecarbonyl isothiocyanate was prepared using the resultant 3,5-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 3,5-dimethyl-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 (39 mg, yield 47%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135466B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-39d7d2021a6c4803a3a713f129fc5114
Quellennotizuspto-grants-2006_11