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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-[4-(pyrrolidin-1-ylcarbonyl)piperid-1-yl]propyl]piperidine hydrochloride | HCID 22741714 | — |
| Edukt | 4-Amino-4-phenylpiperidine dibenzenesulfonate | HCID 22741754 | — |
| Lösungsmittel | acetonitrile N,N-dimethylformamide | HCID 21891449 | — |
| Produkt | 3-[3-(4-Amino-4-phenylpiperid-1-yl)propyl]-1-benzoyl-3-(3,4-dichlorophenyl)-piperidine | HCID 15285591 | 74,6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06710042B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-7452e02e40fe423e8265ad2b71445983 |
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| Quellennotiz | uspto-grants-2004_03 |
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