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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462205Generated: November 1, 2026

Piperazine → HCID 20454108, compound

https://huagongshe.com/reaction/1462205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHexamethyldisilazaneHCID 13838—
ReactantHCID 642154HCID 642154—
ReactantAmmonium SulfateHCID 6097028—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20454108HCID 2045410842%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04459403
Source datasetuspto-grants-1984_07
ORD IDord-439142bfb4d542a685f27f5f462644ec
Source noteuspto-grants-1984_07