HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 20339424, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3,4,4a-Tetrahydro-1H-pyrazino(1,2a)quinoxalin-5-(6H)one | HCID 156362 | — |
| Reactant | 4-(3-Chloropropyl)pyridine | HCID 205442 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20339424 | HCID 20339424 | — |
Reaction Steps
A solution of 6.1 g. (0.03 mole) of 2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)-one, 6.3 g. (0.04 mole) of 3-(4-pyridyl)-1-chloropropane, 10 g. of potassium carbonate, 5 g. of potassium iodide and 0.5 ml. of triethylamine was stirred and refluxed in 200 ml. of acetone for 48 hours, then cooled and filtered. The solvent was removed, and the residue was dissolved in ethanol-ether and treated with dry hydrogen chloride saturated ether. The product hyrochloride was filtered and recrystallized two times from methanol. Dried at 100° C./0.1 mm. Yield: 6.2 g. (44%) as the dihydrochloride salt, m.p. 188°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04203987 |
| Source dataset | uspto-grants-1980_05 |
| ORD ID | ord-81e4b6e868f94e8593a3eee1649ee259 |
| Source note | uspto-grants-1980_05 |