Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1857175Erstellt: 26. Oktober 2026

N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3-nitrophenyl)urea → N-(3-Aminophenyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}urea

https://huagongshe.com/reaction/1857175

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3-nitrophenyl)ureaHCID 11259708—
KatalysatorHCID 178502593HCID 178502593—
LösungsmittelN,N-dimethylformamide ethyl acetateHCID 22989253—
ProduktN-(3-Aminophenyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}ureaHCID 2213277551%

Reaktionsschritte

N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N'-(3-nitrophenyl)urea (28 mg) was dissolved in N,N-dimethylformamide/ethyl acetate (5 ml/2.5 ml), 20% palladium hydroxide-carbon (97 mg) was added, and the admixture was stirred at room temperature under hydrogen for 3 hours. The reaction mixture was filtered using Celite, the filtrate was washed with brine and then dried with anhydrous sodium sulfate. The solvent was then removed by reduced-pressure distillation to obtain 13 mg of the title compound (yield: 51%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06143764
Quelldatensatzuspto-grants-2000_11
ORD IDord-805ad1393c7e4bbfb2305e195a563881
Quellennotizuspto-grants-2000_11