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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50073Erstellt: 23. Oktober 2026

Potassium Carbonate → 3-[3-(4-Amino-4-phenylpiperid-1-yl)propyl]-1-benzoyl-3-(3,4-dichlorophenyl)-piperidine

https://huagongshe.com/de/reaction/50073

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-[4-(pyrrolidin-1-ylcarbonyl)piperid-1-yl]propyl]piperidine hydrochlorideHCID 22741714—
Edukt4-Amino-4-phenylpiperidine dibenzenesulfonateHCID 22741754—
Lösungsmittelacetonitrile N,N-dimethylformamideHCID 21891449—
Produkt3-[3-(4-Amino-4-phenylpiperid-1-yl)propyl]-1-benzoyl-3-(3,4-dichlorophenyl)-piperidineHCID 1528559174,6%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 6.81 g of 4-amino-4-phenylpiperidine dibenzenesulfonate, 5.2 g of the compound obtained in step B of EXAMPLE 1 and 6.1 g of K2CO3 in 30 ml of a DMF/acetonitrile mixture (50/50; v/v) is heated at 100° C. for 5 hours. It is concentrated under vacuum, the residue is taken up with water and extracted with AcOEt, the organic phase is washed with water and with saturated NaCl solution and dried over MgSO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica H using a DCM/MeOH mixture (from 99/1; v/v to 85/15; v/v) as the eluent to give 3.6 g of the expected product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710042B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-7452e02e40fe423e8265ad2b71445983
Quellennotizuspto-grants-2004_03