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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721916Erstellt: 25. Oktober 2026

Cyclopropanecarbonyl chloride, 2-phenyl- → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethyl-N'-[(2-phenylcyclopropyl)carbonyl]thiourea

https://huagongshe.com/reaction/721916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopropanecarbonyl chloride, 2-phenyl-HCID 523092—
Edukt2-Phenyl-1-cyclopropanecarbonyl isothiocyanateHCID 21890726—
EduktN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethylamineHCID 21891226—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
Produkt2-Phenyl-1-cyclopropanecarbonyl isothiocyanateHCID 21890726—
ProduktN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethyl-N'-[(2-phenylcyclopropyl)carbonyl]thioureaHCID 7240726153%

Reaktionsschritte

2-Phenyl-1-cyclopropanecarbonyl isothiocyanate was prepared using commercially available 2-phenyl-1-cyclopropanecarbonyl chloride (80 mg) 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 2-phenyl-1-cyclopropanecarbonyl 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 (43 mg, yield 53%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135466B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-3fcea6a5dd0d4d86b507d1bd7d04d35a
Quellennotizuspto-grants-2006_11