HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 20339407, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 18377410 | HCID 18377410 | — |
| Reactant | HCID 20339423 | HCID 20339423 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20339407 | HCID 20339407 | — |
Reaction Steps
To a solution of 6.2 g. (0.03 mole) of 2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)-one, hydrochloride in 200 ml. acetone is added 15 g. of powdered potassium carbonate, 0.5 ml. of triethylamine, 5 g. of potassium iodide, and 7 g. (0.038 mole) of 5-(4-pyridyl)pentyl bromide. The suspension is stirred and refluxed for 72 hours, cooled, and filtered. The filtrate is concentrated under reduced pressure and the residue is dissolved in methylene dichloride, washed with saline, and dried. The dried organic layer is concentrated and the residue purified by column chromatography using Silicar CC-7. This title compound is obtained as base and converted to hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04203987 |
| Source dataset | uspto-grants-1980_05 |
| ORD ID | ord-706e70e2f2584cf983baf16f7d399824 |
| Source note | uspto-grants-1980_05 |