HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 1-Piperazinecarboxamide, N-methyl-N-((methylamino)carbonyl)-4-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | 2,4-Dimethylallophanoyl chloride | HCID 12226934 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Piperazinecarboxamide, N-methyl-N-((methylamino)carbonyl)-4-phenyl- | HCID 3066934 | 72.6% |
Reaction Steps
Into 40 ml of dichloromethane, was dissolved 6.5 g of 1-phenylpiperazine. To the solution, while being stirred and cooled in ice, was added dropwise 3.0 g of 2,4-dimethylallophanoyl chloride. After 0.5 hour of reaction at room temperature, the reaction mixture was washed with water and dried over anhydrous sodium sulfate. The solvent was removed by distillation and the residue was recrystallized from a mixture of ethanol and petroleum ether to obtain 4.0 g (72% yield) of 1-(2,4-dimethyl-allophanoyl)-4-phenylpiperazine having a melting point of 79°-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666911 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-95be9d2502e649edbdb9921d6fe62e13 |
| Source note | uspto-grants-1987_05 |