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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 720029Erstellt: 25. Oktober 2026

Pyridine → N-BOC-3(R)-methylsulfonyloxymethyl-piperidine

https://huagongshe.com/reaction/720029

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktMethanesulfonyl chlorideHCID 31297—
Edukttert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-BOC-3(R)-methylsulfonyloxymethyl-piperidineHCID 10108453—

Reaktionsschritte

To a stirred solution of N-BOC-3-piperidinemethanol (0.50 g, 0.002 mmole) in DCM (10 mL) was added dropwise pyridine (2.42 mL, 0.03 mmole) followed by the addition of methanesulfonyl chloride (0.774 mL, 0.01 mmole). The reaction mixture continued stirring at RT overnight. The reaction mixture was quenched with water. The aqueous layer was extracted with EtOAc (3×5 mL). Combined organic layers were dried over Na2SO4 and concentrated to yield a crude oil, 68, which was used in the next step without further purification. LRMS: 193 (M+-BOC group).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07132551B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-cec5e9591b3749c19449595e86e364ad
Quellennotizuspto-grants-2006_11