Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271560Erstellt: 25. Oktober 2026

Cesium carbonate → Tert-butyl 4-(6-fluoropyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/271560

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
EduktBinap, (A+-)-HCID 634876—
EduktTert-butyl Piperazine-1-carboxylate HydrochlorideHCID 2755973—
Edukt5-Bromo-2-fluoropyridineHCID 2783168—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 4-(6-fluoropyridin-3-yl)piperazine-1-carboxylateHCID 5983473543%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A suspension of piperazine-1-carboxylic acid tert-butyl ester hydrochloride (0.75 mmol), 5-bromo-2-fluoropyridine (0.90 mmol), (R)-2,2′-bis(diphenylphosphino)-1, 1′-binaphthyl (0.038 mmol), palladium acetate (0.038 mmol) and cesium carbonate (1.8 mmol) in toluene is stirred at 80° C. for 7 h and then 100° C. for 4 h, and poured into water. The mixture is extracted with AcOEt. The organic layer is washed with water, dried over magnesium sulfate, and concentrated. The crude product is purified by silica gel column chromatography to give the product in 43% yield. Rf=0.61 (n-hexane:AcOEt=1:1)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07452886B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-61ffb66676194eb78c51d58eeeef3fb6
Quellennotizuspto-grants-2008_11