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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 228637Erstellt: 24. Oktober 2026

1,2-Dichlorobenzene → N-Phenyl-5-chloro-2-[(6,7-dimethoxy-4-quinolyl)oxy]-benzamide

https://huagongshe.com/de/reaction/228637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichlorobenzeneHCID 7239—
EduktBenzamide, N-(4-chlorophenyl)-2-hydroxy-HCID 77253—
Edukt4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
ProduktN-Phenyl-5-chloro-2-[(6,7-dimethoxy-4-quinolyl)oxy]-benzamideHCID 5775642720%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

4-Chloro-6,7-dimethoxyquinoline (100 mg), 4′-chloro-salicylanilide (445 mg), and 4-dimethylaminopyridine (220 mg) were suspended in o-dichlorobenzene (1 ml), and the suspension was stirred at 140° C. for 4 hr. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-hexane to give the title compound (38 mg, yield 20%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560558B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-74797ef604f641848eec90d7f66fdfbb
Quellennotizuspto-grants-2009_07