HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 20454108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | HCID 642154 | HCID 642154 | — |
| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20454108 | HCID 20454108 | 42% |
Reaction Steps
A solution of 1.16 g (0.010 of 6H-1,2,4-oxadiazin-3,5-(2H,4H)-dione, 5 mg of ammonium sulfate, 2.49 g (0.029 mole) of piperazine and 20 ml of hexamethyldisilazane in 40 ml of dry freshly distilled dioxane is refluxed for 17 hours. After cooling, the dioxane and hexamethyldisilazane are removed in vacuo and the syrupy residue is dried on a vacuum pump for 2 hours. The resulting semi-solid residue is triturated with 100 ml of petroleum ether and filtered to yield 0.78 g (42 percent) of 5-(1-piperazinyl)-6H-1,2,4-oxadiazin-3(2H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04459403 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-439142bfb4d542a685f27f5f462644ec |
| Source note | uspto-grants-1984_07 |