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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54561Erstellt: 24. Oktober 2026

Water → 3-[3-(1-Benzylpiperidin-4-yl)propyl]-5-(quinuclidin-3-yl)-1,2,4-oxadiazole

https://huagongshe.com/de/reaction/54561

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
EduktMethyl quinuclidine-3-carboxylateHCID 2736953—
Edukt4-(1-Benzylpiperidin-4-yl)butanamide oximeHCID 86750726—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-[3-(1-Benzylpiperidin-4-yl)propyl]-5-(quinuclidin-3-yl)-1,2,4-oxadiazoleHCID 1995916043,8%

Reaktionsschritte

A mixture of 4-(1-benzylpiperidin-4-yl)butanamide oxime (1.0 g), sodium hydride (0.15 g) and molecular sieves 4A (2.0 g) in tetrahydrofuran (50 ml) was stirred at ambient temperature for 30 minutes. To the mixture was added dropwise a solution of methyl 3-quinuclidine carboxylate (0.49 g) in tetrahydrofuran (10 ml) and refluxed for 6 hours. After cooling to room temperature, the mixture was poured into water and extracted with ethyl acetate. The extracts were successively washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on alumina eluting with chloroform to give 3-[3-(1-benzylpiperidin-4-yl)propyl]-5-(quinuclidin-3-yl)-1,2,4-oxadiazole (0.5 g) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05622976
Quelldatensatzuspto-grants-1997_04
ORD IDord-50dec5ff3d014dcb9434de57ce76d919
Quellennotizuspto-grants-1997_04