HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → HCID 15233926, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | HCID 19024280 | HCID 19024280 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 15233926 | HCID 15233926 | 72.5% |
Reaction Steps
To a solution of 69.4 mg of the compound of Example 16 dissolved in 10 ml of dioxane was added 109 mg (3 equivalents) of N-phenylpiperazine, and the mixture heated under reflux for 17 hours. The reaction treatment and purification were conducted in the same manner as in Example 17 to obtain 63.5 mg of the desired compound (yield 72.5%). The fumarate was obtained by converting the product to fumarate in a conventional manner, followed by recrystallization from acetoneether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05312625 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-39545351c7df427abd1ad5805973b23e |
| Source note | uspto-grants-1994_05 |