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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494402Erstellt: 24. Oktober 2026

1-Benzyl-4-(4'-trifluoromethylbiphenyl-2-carbonylamino)piperidine → N-(Piperidin-4-yl)-4'-(trifluoromethyl)-biphenyl-2-carboxamide

https://huagongshe.com/de/reaction/494402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzyl-4-(4'-trifluoromethylbiphenyl-2-carbonylamino)piperidineHCID 22995692—
KatalysatorPalladium hydroxideHCID 9942167—
LösungsmittelTetrahydrofurfuryl alcoholHCID 7360—
ProduktAmmoniaHCID 222—
ProduktN-(Piperidin-4-yl)-4'-(trifluoromethyl)-biphenyl-2-carboxamideHCID 9928271176,4%

Reaktionsschritte

To a solution of the 1-benzyl-4-(4′-trifluoromethylbiphenyl-2-carbonylamino)piperidine (1.47 g) obtained in Example 8a) in tetrahydrofuran-methanol (1:1; 50 mL) was added palladium hydroxide (300 mg) in a stream of argon under ice-cooling. The mixture was stirred for one day at normal pressure under hydrogen atmosphere, and further stirred for one day at normal pressure under hydrogen atmosphere after further addition of palladium hydroxide (300 mg). The reaction mixture was filtered through a Celite pad and washed with methanol. The filtrate and the washings were combined, concentrated in vacuo and purified by column chromatography on silica gel with chloroform:methanol:aqueous ammonia=100:10:1 to give the title compound (1.03 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538140B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-acf22412513b4430899df264ef800621
Quellennotizuspto-grants-2009_05