HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenylpiperidine-4-carboxamide monohydrochloride | HCID 3017129 | — |
| Reactant | 2-[3-(3,4-Dichloro-phenyl)-1-(3,5-dimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl-methanesulfonate | HCID 23194310 | — |
| Product | 2-[3-(3,4-Dichloro-phenyl)-1-(3,5-dimethoxy-benzoyl)-pyrrolidin-3-yl-ethyl]-4-phenyl-piperidine-4-carboxylic acid amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05635510 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-fd7b279c7e734274a91713a9aac780dd |
| Source note | uspto-grants-1997_06 |