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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267153Generated: October 31, 2026

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

https://huagongshe.com/reaction/2267153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHydroxylamine HClHCID 21645—
Reactanttert-Butyl 4-cyanopiperazine-1-carboxylateHCID 14068968—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Producttert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylateHCID 17845234686.4%

Reaction Steps

In a nitrogen atmosphere, a suspension of 7.52 g of tert-butyl 4-cyanopiperazine-1-carboxylate (JMC, 1988, 31, 1036), 7.46 g of hydroxyammonium chloride and 19.7 g of potassium carbonate in 40 ml of ethanol was heated to reflux for 2 hours. The residue prepared by evaporation of the solvent was diluted with ethyl acetate, washed with water and then with a saturated saline solution and dried over sodium sulfate. The solvent was evaporated in vacuo to give 7.51 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858800B2
Source datasetuspto-grants-2010_12
ORD IDord-7907d2e4b2ce4cc387d562b55774d64c
Source noteuspto-grants-2010_12