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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494401Erstellt: 24. Oktober 2026

4'-(Trifluoromethyl)(1,1'-biphenyl)-2-carboxylic acid → 1-Benzyl-4-(4'-trifluoromethylbiphenyl-2-carbonylamino)piperidine

https://huagongshe.com/de/reaction/494401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4'-(Trifluoromethyl)(1,1'-biphenyl)-2-carboxylic acidHCID 55251—
Edukt1-Benzyl-4-piperidylamineHCID 415852—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Benzyl-4-(4'-trifluoromethylbiphenyl-2-carbonylamino)piperidineHCID 2299569290,7%

Reaktionsschritte

4′-Trifluoromethyl-biphenyl-carboxylic acid (5.0 g) was dissolved in dimethylformamide (50 mL), and to this solution were added at room temperature 4-amino-1-benzylpiperidine (3.55 g), 1-hydroxybenzotriazole hydrate (3.0 g) and 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride (3.58 g). The mixture was stirred at room temperature overnight, and the reaction solution was concentrated in vacuo to precipitate crystals. The crystals were washed successively with saturated aqueous sodium bicarbonate and water, and dried in vacuo to give the title compound (7.42 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538140B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-a99ba96bcbe94e9f809d866deea4b699
Quellennotizuspto-grants-2009_05