HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 8-Azaspiro(4.5)decane-7,9-dione, 8-(4-(4-(5-methoxy-1H-indol-3-yl)-1-piperidinyl)butyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Methoxy-3-(piperidin-4-yl)-1H-indole | HCID 43224 | — |
| Reactant | HCID 86743285 | HCID 86743285 | — |
| Product | 8-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855302 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-fd829c56d3214d779d39c0b9dbfe9085 |
| Source note | uspto-grants-1989_08 |