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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15852Erstellt: 23. Oktober 2026

Cesium carbonate → 2-Methyl-5-[(3R)-3-methyl-1-piperazinyl]quinoline

https://huagongshe.com/de/reaction/15852

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
EduktBinap, (A+-)-HCID 634876—
Edukt2-Methylpiperazine, (R)-HCID 7330434—
Edukt2-Methylquinolin-5-yl trifluoromethanesulfonateHCID 49851899—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelTolueneHCID 1140—
Produkt2-Methyl-5-[(3R)-3-methyl-1-piperazinyl]quinolineHCID 5744433958%

Reaktionsschritte

(2R)-2-Methylpiperazine (0.550 g; 2 eq), caesium carbonate (1.78 g; 2 eq), palladium acetate (0.123 g; 0.2 eq) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.513 g; 0.3 eq) were added to a solution of 2-methyl-5-quinolinyl trifluoromethanesulfonate (D1) (0.8 g; 1 eq) in toluene (30 mL) under an inert atmosphere. The reaction mixture was stirred at reflux under nitrogen for 3 hours. The reaction cooled to room temperature, quenched using saturated aqueous ammonium chloride solution (15 mL) and extracted with ethyl acetate (3×20 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure. The crude was purified by flash chromatography on silica gel, eluting with dichloromethane-methanol (95:5) affording the title compound in 58% yield (0.383 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732600B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-cf90e6509db44c63a078279acad2d9c7
Quellennotizuspto-grants-2010_06