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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744133Generated: October 31, 2026

HCID 69151040, compound → HCID 69152735, compound

https://huagongshe.com/reaction/1744133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69151040HCID 69151040—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 69152735HCID 69152735—

Reaction Steps

To 4-methoxybenzyl N-(1-(tert-butoxycarbonyl)4-{4-[4-(tert-butoxycarbonyl)piperazin-1-yl]phenyl}-1H-pyrazol-3-yl)leucinate (1.14 g, 1.68 mmol) in EtOH (30 mL) was added the catalyst palladium on carbon (10%, 500 mg) and the reaction was stirred under a hydrogen atmosphere overnight. After degassing with nitrogen, CH2Cl2 was added and the reaction mixture was filtered on celite, washed with EtOH, concentrated in vacuo and purified by flash chromatography over silica gel (AcOH/EtOAc/Hex, 1/49/50) to afford N-(1-(tert-butoxycarbonyl)-4-{4-[4-(tert-butoxycarbonyl)piperazin-1-yl]phenyl}-1H-pyrazol-3-yl)leucine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012075B2
Source datasetuspto-grants-2006_03
ORD IDord-47648e10a9494e28bec2f81dd787e0c2
Source noteuspto-grants-2006_03