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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775319Generated: November 2, 2026

Triethylamine → tert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylate

https://huagongshe.com/reaction/1775319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactanttert-Butyl 4-cyanopiperazine-1-carboxylateHCID 14068968—
SolventEthanolHCID 702—
Producttert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylateHCID 178452346100.7%

Reaction Steps

To a solution of tert-butyl 4-cyanopiperazine-1-carboxylate (1.22 g, 5.77 mmol) in anhydrous ethanol (10 mL) were added hydroxylamine hydrochloride (420 mg, 6.04 mmol) and triethyl amine (843 L, 6.06 mmol). The reaction was heated to reflux for 45 min, after which TLC showed complete consumption of the starting material. The mixture was allowed to cool to room temperature overnight, and the resulting precipitate was removed by filtration. The filtrate was concentrated, yielding 1.42 g of a yellow gel that was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-3c2ded138b444e7cb9954cadb0ff5ad5
Source noteuspto-grants-2016_02