HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Cyclohexylpiperazine → HCID 22870248, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Cyclohexylpiperazine | HCID 87298 | — |
| Reactant | HCID 86750415 | HCID 86750415 | — |
| Product | HCID 22870248 | HCID 22870248 | — |
Reaction Steps
In 30 ml of acetonitrile (R)-3-(2-methanesulfonyloxyethyl)-3-(3,4-dichlorophenyl)-1-[(2-chloro-6-fluorophenyl)acetyl]pyrrolidine (3.17 g), prepared as described, supra, is mixed with an equimolar amount of 1-cyclohexylpiperazine. The reaction mixture is then heated to reflux and refluxed for about ten hours. The mixture is then concentrated under vacuum and the residue is taken up in methylene chloride and washed with a 3N solution of hydrochloric acid, followed by a wash with brine. The organic fraction is dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue precipitates from an acetone/diethyl ether mixture to give the desired title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05607947 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-0f9f21d7bce043588649174876637e27 |
| Source note | uspto-grants-1997_03 |