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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757756Generated: November 2, 2026

1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide → Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1757756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamideHCID 19031938—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylateHCID 406301358.8%

Reaction Steps

1.1 g of 1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide were dissolved in 40 ml of ethanol. 0.1 g of 10% palladium-on-carbon was added and the mixture was hydrogenated at room temperature and under atmospheric pressure for 2 hours. The catalyst was filtered off. The filtrate was evaporated to give 0.74 g of crude product which was purified by flash chromatography on silica gel using 5% methanolin dichloromethane for the elution. After evaporation of the solvents therewas obtained 0.44 g of 4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide as an oil: MS: m/e 286 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446161
Source datasetuspto-grants-1995_08
ORD IDord-3005a8f761bd40d1a588fdf4dfed825a
Source noteuspto-grants-1995_08