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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721907Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/721907

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
Edukt3-(2-Methylphenyl)propionic acidHCID 30938—
Edukt4-(6,7-Dimethoxyquinazolin-4-yloxy)anilineHCID 11616363—
Edukt3-(2-Methylphenyl)propanoyl chlorideHCID 13029201—
Edukt3-(2-Methylphenyl)propanoyl isothiocyanateHCID 21890701—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
ProduktN-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[3-(2-methylphenyl)propanoyl]thioureaHCID 2188995757%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 3-(2-methylphenyl)propanoic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 3-(2-methylphenyl)propanoyl isothiocyanate was prepared using the resultant 3-(2-methylphenyl)propanoyl chloride as a starting compound according to the description of the literature. 4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]aniline (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 3-(2-methylphenyl)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 (48 mg, yield 57%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135466B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-35ea3f3fc5f64d2f83ebe787358ae9e2
Quellennotizuspto-grants-2006_11