Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1504202Erstellt: 25. Oktober 2026

Methanol → 1-methyl-6-[3-(quinolin-6-ylamino)propoxy]-1H-quinolin-2-one

https://huagongshe.com/reaction/1504202

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt6-AminoquinolineHCID 11373—
Edukt6-(3-iodopropoxy)-1-methyl-1H-quinolin-2-oneHCID 66960607—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-methyl-6-[3-(quinolin-6-ylamino)propoxy]-1H-quinolin-2-oneHCID 6696154748%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

6-Aminoquinoline(360 mg) was added to the methanol solution(10 ml) of 6-(3-iodopropoxy)-1-methyl-1H-quinolin-2-one(172 mg) and stirred at 60° C. for 17 hours. The reaction mixture was added to ice water, and extraction with dichloromethane was performed. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate: methanol=10:0→4:1). The purified product was condensed under reduced pressure to give the title compound(86.4 mg) as a yellow amorphous solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09212187B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-407ad6b5484b43eba21dcedd0c932c71
Quellennotizuspto-grants-2015_12