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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54100Generated: October 25, 2026

Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylate → 1-Piperazinecarboxamide

https://huagongshe.com/reaction/54100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylateHCID 4063013—
Reactant(2S,3S)-1,2-Epoxy-3-(Cbz-amino)-4-phenylbutaneHCID 9861019—
SolventIsopropanolHCID 3776—
Product1-PiperazinecarboxamideHCID 258192—

Reaction Steps

0.395 g of 4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide was dissolved in 50 ml of dry isopropanol and treated with 0.413 g of 3(S)-(benzyloxyformamido)-1,2(S)-epoxy-4-phenylbutane. The mixture was stirred at room temperature for 72 hours. The solvent was removed by evaporation to give a brown semi-solid material which was purified by flash chromatography on silica gel using 5% methanol in dichloromethane for the elution. There was obtained 0.234 g of 1-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-4-(tert.butoxycarbonyl)-N-tert.butyl-2(R or S)-piperazinecarboxamide as a mixture of diastereomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620987
Source datasetuspto-grants-1997_04
ORD IDord-c7b15625057f47b2ab0684bbedde28e0
Source noteuspto-grants-1997_04