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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54559Erstellt: 25. Oktober 2026

2-(1-Benzylpiperidin-4-yl)ethan-1-amine → 5-(Quinuclidin-3-yl)-3-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]-1,2,4-oxadiazole

https://huagongshe.com/reaction/54559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(1-Benzylpiperidin-4-yl)ethan-1-amineHCID 1867002—
Edukt3-Ethoxycarbonyl-5-(quinuclidin-3-yl)-1,2,4-oxadiazoleHCID 14685546—
Produkt5-(Quinuclidin-3-yl)-3-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]-1,2,4-oxadiazoleHCID 19959165—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 3-ethoxycarbonyl-5-(quinuclidin-3-yl)-1,2,4-oxadiazole (0.2 g) and 1-benzyl-4-(2-aminoethyl)piperidine (0.26 g) was stirred and heated at 100° C. for 2 hours. The cooled mixture was chromatographed on alumina eluting with chloroform to give 5-(quinuclidin-3-yl)-3-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]-1,2,4-oxadiazole as an oil. The compound was treated with an ethanol solution of hydrogen chloride, the solution was evaporated in vacuo and the residue was powdered with ether to give 5-(quinuclidin-3-yl)-3-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]-1,2,4-oxadiazole dihydrochloride (0.2 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05622976
Quelldatensatzuspto-grants-1997_04
ORD IDord-f63717e5f49849a488f00827e3ebbd54
Quellennotizuspto-grants-1997_04