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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403615Generated: November 1, 2026

HCID 68106402, compound → HCID 70570910, compound

https://huagongshe.com/reaction/2403615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68106402HCID 68106402—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70570910HCID 7057091074.9%

Reaction Steps

Benzyl 4-[3′-({[N-(tert-butoxycarbonyl)glycyl](methyl)amino}methyl)biphenyl-4-yl]piperazine-1-carboxylate (1.5 g) was dissolved in a mixed solution of MeOH (15 ml) and THF (15 ml). 10% Pd—C (150 mg) was added thereto, followed by stirring at room temperature for 1 day under a hydrogen atmosphere. The reaction mixture was filtered using Celite as a filtration assistant, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain tert-butyl (2-{methyl [(4′-piperazin-1-ylbiphenyl-3-yl)methyl]amino}-2-oxoethyl)carbamate (860 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802679B2
Source datasetuspto-grants-2014_08
ORD IDord-a9483bd5ec7a4b1c8ac9cb303b5cdf6e
Source noteuspto-grants-2014_08