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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50655Erstellt: 26. Oktober 2026

1-(2-Methoxyphenyl)piperazine → 3-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/50655

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(2-Methoxyphenyl)piperazineHCID 1346—
EduktPotassium CarbonateHCID 11430—
Edukttert-Butyl 3-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylateHCID 22647269—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 21303201—

Reaktionsschritte

To a solution of 3-methanesulfonyloxymethyl-piperidine-1-carboxylic acid tert-butyl ester (11.06 g, 0.04 mol) in acetonitrile (180 mL) was added potassium carbonate (26 g, 0.19 mol) followed by 1-(2-methoxy-phenyl) piperazine (7.25 g, 0.04 mol). After completion of addition the reaction mixture was heated to reflux. After 12 h the reaction mixture was cooled down to room temperature and quenched with water. The aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organic layers were dried over sodium sulfate and concentrated to yield an oil. This crude material was purified using silica gel chromatography (7:3:0.05 Hexane:EtOAc:2M NH3 in EtOH) to afford the desired compound in good yield (8.0 g, 55%). C22H35N3O3,LRMS (m/z)=390 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713479B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-8ae9b22ad09f41dfbaab188226486b1d
Quellennotizuspto-grants-2004_03