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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597094Generated: October 26, 2026

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

https://huagongshe.com/reaction/1597094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Benzoyl-3-(3,4-dichlorophenyl)-3-[3-(methanesulfonyloxy)propyl]piperidineHCID 11812710—
Reactant4-Amino-4-phenylpiperidine dibenzenesulfonateHCID 22741754—
Solventacetonitrile N,N-dimethylformamideHCID 21891449—
Product3-[3-(4-Amino-4-phenylpiperid-1-yl)propyl]-1-benzoyl-3-(3,4-dichlorophenyl)-piperidineHCID 1528559159.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291672B1
Source datasetuspto-grants-2001_09
ORD IDord-857efcdcda5a48a29602cd1ec137f25e
Source noteuspto-grants-2001_09