Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399968Generated: October 26, 2026

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

https://huagongshe.com/reaction/399968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Phenylpiperidine-4-carboxamide monohydrochlorideHCID 3017129—
Reactant2-[1-(2,4-Dimethoxy-benzoyl)-3-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethyl-methanesulfonateHCID 86750905—
SolventTetrahydrofuranHCID 8028—
Product1-[2-[3-(3,4-Dichloro-phenyl)-1-(2,4-dimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid amideHCID 4421228436.4%

Reaction Steps

2-[1-(2,4-Dimethoxy-benzoyl)-3-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethyl-methanesulfonate (343 mg, 0.68 mmol) was dissolved in THF (8 mL) and the 4-phenyl-piperidine-4-carboxylic acid amide hydrochloride (170 mg, 0.71 mmol, 1.04 eq.), potassium carbonate (200 mg, 1.45 mmol, 2.1 eq.), and water (2 mL) were added and the solution was heated at reflux for 16 hours. The solution was concentrated in vacuo and the aqueous phase was extracted with dichloromethane, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel (40 g) with a gradient of ethyl acetate to 6% methanol in dichloromethane to give 151 mg (36%) of the title compound. Analysis: calculated for C33H37Cl2N3O4.0.6 H2O C 63.86; H 6.20; N 6.76. Found C 63.61; H 6.13; N 6.67.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05824690
Source datasetuspto-grants-1998_10
ORD IDord-b97b817277074793a2f002eaf6be63c8
Source noteuspto-grants-1998_10