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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989854Generated: November 4, 2026

N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamide → 4'-Trifluoromethyl-biphenyl-2-carboxylic acid [4-(piperazinyl)-phenyl]-amide

https://huagongshe.com/reaction/1989854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamideHCID 22499401—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4'-Trifluoromethyl-biphenyl-2-carboxylic acid [4-(piperazinyl)-phenyl]-amideHCID 11201099—

Reaction Steps

A mixture of intermediate (1) (0.19 mol) in methanol (600 ml) and THF (600 ml) was hydrogenated overnight with palladium on carbon (10%; 3 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 DIPE. The precipitate was filtered off and dissolved in water. The mixture was alkalized with Na2CO3 and then extracted with DCM. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was triturated in DIPE. The precipitate was filtered off and dried, yielding N-[4-(1-piperazinyl)phenyl]-4′-(trifluoromethyl)-[1,1′-biphenyl]-2-carboxamide (intermediate 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642378B2
Source datasetuspto-grants-2010_01
ORD IDord-924f4b2c07ec456294b2e784cf8caad6
Source noteuspto-grants-2010_01