HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → HCID 15788933, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 20097024 | HCID 20097024 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15788933 | HCID 15788933 | — |
Reaction Steps
A mixture of 3.56 g (15 mmol) of N-(4-bromo-butyl)-4-chloropyrazole, 2.43 g (15 mmol) of 1-phenyl-piperazine and 2.76 g (20 mmol) of potassium carbonate in 50 ml of dimethylformamide is refluxed for 24 hours. The reaction mixture is evaporated under vacuum, chloroform is added, the mixture is washed with water, dried over sodium sulphate and evaporated under vacuum and 3.1 g of 4-chloro-1-[4-(4-phenyl-1-piperazinyl)-butyl]-1H-pyrazole are obtained, which may be recrystallised from ethyl ether with a melting point of 58°-61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292739 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-93cb3eb348914d13884b42ba49102c6f |
| Source note | uspto-grants-1994_03 |