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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15768Erstellt: 24. Oktober 2026

Cesium carbonate → Tert-butyl 4-(2-methylquinolin-5-yl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/15768

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
EduktBinap, (A+-)-HCID 634876—
Edukt2-Methylquinolin-5-yl trifluoromethanesulfonateHCID 49851899—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelTolueneHCID 1140—
ProduktTert-butyl 4-(2-methylquinolin-5-yl)piperazine-1-carboxylateHCID 4985190062%

Reaktionsschritte

tert-Butyl 1-piperazine carboxylate (1.6 g; 1.2 eq), cesium carbonate (1.7 g; 1.5 eq), palladium acetate (0.33 g; 0.14 eq) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.97 mg; 0.15 eq) were added to a solution of 2-methyl-5-quinolinyl trifluoromethanesulfonate (D1) in toluene (20 mL) under an inert atmosphere. The reaction mixture was stirred at reflux under nitrogen for 8 hours. The reaction was quenched at room temperature using a saturated aqueous solution of ammonium chloride (15 mL) and extracted into ethyl acetate (3×20 mL). The organic layers were combined, dried over Na2SO4 and concentrated under reduced pressure. The crude was purified by flash chromatography, eluting with ethyl acetate/cyclohexane (3/7) affording the title compound in 62% yield (1.4 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732600B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-8a5315f9c363403ea8321f3dfc2a3dea
Quellennotizuspto-grants-2010_06