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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991362Generated: November 3, 2026

(+/-)-cis-1-[3,5-Bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-[4-(phenylmethyl)-1-piperazinyl]piperidine → (+/-)-1-[3,5-Bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-(1-piperazinyl)piperidine

https://huagongshe.com/reaction/991362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-cis-1-[3,5-Bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-[4-(phenylmethyl)-1-piperazinyl]piperidineHCID 86619157—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(+/-)-1-[3,5-Bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-(1-piperazinyl)piperidineHCID 18630855100%

Reaction Steps

A mixture of compound 16 (8.4 g) in methanol (250 ml) was hydrogenated at 50° C. with palladium on activated carbon (10%) (2 g) as a catalyst. After uptake of H2, the catalyst was filtered off and the filtrate was evaporated; yielding 7 g (100%) of (±)-1-[3,5-bis(trifluoromethyl) benzoyl]-2-(phenylmethyl)-4-(1-piperazinyl)piperidine (compound 15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037886E1
Source datasetuspto-grants-2002_10
ORD IDord-5129abb5c3b84e8e9f99cc07c781dd67
Source noteuspto-grants-2002_10