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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804429Generated: October 31, 2026

N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-[1,1'-biphenyl]-2-carboxamide → N-[4-(1-piperazinyl)phenyl]-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/1804429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-[1,1'-biphenyl]-2-carboxamideHCID 22499373—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-[4-(1-piperazinyl)phenyl]-[1,1'-biphenyl]-2-carboxamideHCID 2249936981.1%

Reaction Steps

A mixture of intermediate (9) (0.1 mole) in methanol (500 ml) was hydrogenated for two hours with palladium-on-carbon (10%) (10 g) as a catalyst. After uptake of hydrogen (1 equivalent), the catalyst was filtered off and the filtrate was evaporated. The residue was triturated in 2-propanol. The precipitate was filtered off and dried, yielding 29 g of N-[4-(1-piperazinyl)phenyl]-[1,1′-biphenyl]-2-carboxamide (intermediate 10, melting point 176° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354402B2
Source datasetuspto-grants-2013_01
ORD IDord-199a44b75cd042d397704bed6b3d428f
Source noteuspto-grants-2013_01