Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1697089Erstellt: 26. Oktober 2026

Potassium Carbonate → 2-acetyl-7-chloro-3-[4-(4-hydroxypiperidine-1-sulfonyl)-benzyl]-1-phenyl-1H-quinolin-4-one

https://huagongshe.com/reaction/1697089

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktN-(5-chloro-2-{3-[4-(4-hydroxypiperidine-1-sulfonyl)-phenyl]-propionyl}-phenyl)-2-oxo-N-phenyl-propionamideHCID 66817005—
LösungsmittelMethanolHCID 887—
Produkt2-acetyl-7-chloro-3-[4-(4-hydroxypiperidine-1-sulfonyl)-benzyl]-1-phenyl-1H-quinolin-4-oneHCID 59846195—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To N-(5-chloro-2-{3-[4-(4-hydroxypiperidine-1-sulfonyl)-phenyl]-propionyl}-phenyl)-2-oxo-N-phenyl-propionamide in MeOH was added K2CO3 (0.096 g), and the mixture heated at 80° C. for 1.5 h, then concentrated. The residue was taken up in EtOAc/H2O, and the aqueous layer washed with EtOAc (2×25 mL). The combined organic layers were dried over Na2SO4, and the solvent removed under reduced pressure. The residue was chromatographed on anhydrous silica (20% EtOAc/hexanes 0-5 min; 60% EtOAc/hexanes 15-20 min; 100% EtOAc 22-35 min) to provide 2-acetyl-7-chloro-3-[4-(4-hydroxypiperidine-1-sulfonyl)-benzyl]-1-phenyl-1H-quinolin-4-one (compound 70). Mp=145.5-147.2° C.; M+H 551.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163906B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-a6f655b445d240e496b4ad5c96638f30
Quellennotizuspto-grants-2012_04