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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682982Generated: November 3, 2026

4-Phenylpiperidine-4-carboxamide monohydrochloride → 2-[3-(3,4-Dichloro-phenyl)-1-(3,5-dimethoxy-benzoyl)-pyrrolidin-3-yl-ethyl]-4-phenyl-piperidine-4-carboxylic acid amide

https://huagongshe.com/reaction/1682982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenylpiperidine-4-carboxamide monohydrochlorideHCID 3017129—
Reactant2-[3-(3,4-Dichloro-phenyl)-1-(3,5-dimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl-methanesulfonateHCID 23194310—
Product2-[3-(3,4-Dichloro-phenyl)-1-(3,5-dimethoxy-benzoyl)-pyrrolidin-3-yl-ethyl]-4-phenyl-piperidine-4-carboxylic acid amideHCID 86750911—

Reaction Steps

The method of example 3.3 was used with 2-[3-(3,4-dichloro-phenyl)-1-(3,5-dimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl-methanesulfonate (0.96 mmol) and 4-phenylpiperidine-4-carboxylic acid amide hydrochloride (1.06 mmol) to prepare the title compound. Chromatography on silica gel eluting sequentially with ethyl acetate, 6% methanol in dichloromethane, and then 10% methanol in dichloromethane gave the title compound:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05635510
Source datasetuspto-grants-1997_06
ORD IDord-fd7b279c7e734274a91713a9aac780dd
Source noteuspto-grants-1997_06