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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722307Generated: October 31, 2026

Sodium Iodide → 8-Azaspiro(4.5)decane-7,9-dione, 8-(4-(4-(5-methoxy-1H-indol-3-yl)-1-piperidinyl)butyl)-

https://huagongshe.com/reaction/1722307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantSodium CarbonateHCID 10340—
Reactant5-Methoxy-3-(piperidin-4-yl)-1H-indoleHCID 43224—
ReactantHCID 86743285HCID 86743285—
Product8-Azaspiro(4.5)decane-7,9-dione, 8-(4-(4-(5-methoxy-1H-indol-3-yl)-1-piperidinyl)butyl)-HCID 3088095—

Reaction Steps

A mixture of 2.3 g of 5-methoxy-3-(4-piperidinyl)-1H-indole, 2.58 g of 8-[4-chlorobutyl-8-azaspiro[4,5]decane-7,9-dione, 2.12 g of sodium carbonate, 150 mg of sodium iodide and 50 ml of butanone was refluxed under an inert atmosphere with stirring for 20 hours and after another 1.29 g of the dione were added. Reflux was continued for 6 hours. The mixture was filtered and washed with acetone and the filtrate was evaporated to dryness. The residue was crystallized from 60% ethanol to obtain 3.4 g of 8-[4-{4-(5-methoxy-1H-indol-3-yl)-1-piperidinyl}-butyl]-8-azaspiro[4,5]decane-7,9-dione melting at ≈150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855302
Source datasetuspto-grants-1989_08
ORD IDord-fd829c56d3214d779d39c0b9dbfe9085
Source noteuspto-grants-1989_08