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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639326Generated: October 25, 2026

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

https://huagongshe.com/reaction/1639326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant8-Azaspiro(4.5)decane-7,9-dioneHCID 136843—
Reactant4-Pyridinylbutyl bromide hydrobromideHCID 70354558—
Product8-[4-(4-Pyridinyl)butyl]-8-azaspiro[4.5]decane-7,9-dioneHCID 1592573530%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04883875
Source datasetuspto-grants-1989_11
ORD IDord-2eeac32f7cfd427b9f3b3d45cb31da9e
Source noteuspto-grants-1989_11