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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852454Generated: November 1, 2026

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

https://huagongshe.com/reaction/852454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-[1-(phenylmethyl)-4-piperidinyl]phenyl]-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamideHCID 22499370—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-[4-(4-piperidinyl)phenyl]-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamideHCID 2249936872.6%

Reaction Steps

A mixture of intermediate (16) (0.025 mol) in methanol (250 ml) was hydrogenated at 50° C. overnight with Pd/C 10% (2 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 dried, yielding 7.7 g N-[4-(4-piperidinyl)phenyl]-4′-(trifluoromethyl)-[1,1′-biphenyl]-2-carboxamide (intermediate 17).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253157B2
Source datasetuspto-grants-2007_08
ORD IDord-ad7009f7bb144796aa69cc58afaf7489
Source noteuspto-grants-2007_08