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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1199486Erstellt: 25. Oktober 2026

Dimethylformamide → 8-[4-(4-Pyridinyl)butyl]-8-azaspiro[4.5]decane-7,9-dione

https://huagongshe.com/reaction/1199486

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktCesium carbonateHCID 10796—
Edukt8-Azaspiro(4.5)decane-7,9-dioneHCID 136843—
Edukt4-Pyridinylbutyl bromide hydrobromideHCID 70354558—
Produkt8-[4-(4-Pyridinyl)butyl]-8-azaspiro[4.5]decane-7,9-dioneHCID 1592573530%

Reaktionsschritte

To a stirred solution of 1.8 g. (0.011 mol) of 3,3-tetramethyleneglutarimide in 50 ml. of dimethylformamide is added 3 g. (0.011 mol) of cesium carbonate and 3.2 g. (0.011 mol) of 4-pyridinylbutyl bromide hydrobromide. The reaction mixture is stirred at room temperature for 48 hours, dimethylformamide is evaporated under reduced pressure and the residue is extracted with methylene chloride (3×200 ml.). The methylene chloride extracts are collected, washed with water, dried over anhydrous Na2SO4 and evaporated under reduced pressure. The semisolid residue was subjected to HPLC separated using ethyl acetate as eluent. Evaporation of the solvent from the desired fraction (TLC Rf 0.2) affords 1.0 g. (30% yield) of the titled compound which is converted to the hydrochloride salt by dissolving the free base in ethanol and adding ethanol saturated with hydrogen chloride; m.p. 155°-157° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04900835
Quelldatensatzuspto-grants-1990_02
ORD IDord-64d4e5b8eb75400cb40fd8fc76cd4e8a
Quellennotizuspto-grants-1990_02