HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-Piperazinecarboxamide, N-((methylamino)carbonyl)-4-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 4-Phenylpiperazine-1-carboximidic acid | HCID 250365 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Piperazinecarboxamide, N-((methylamino)carbonyl)-4-phenyl- | HCID 3066929 | 51.5% |
Reaction Steps
Into 70 ml of dichloromethane, were dissolved 4.1 g of 4-phenylpiperazine-1-carboxamide and 1.2 g of methyl isocyanate. To the solution, while being stirred and cooled in ice, was added dropwise 5.2 g of stannic chloride. After 15 hours of reaction at room temperature, water was added to separate an organic layer. The organic layer was dried over anhydrous sodium sulfate and freed from the solvent by distillation. The residue was recrystallized from ethanol to obtain 2.7 g (51% yield) of 1-(4-methylallophanoyl)-4-phenylpiperazine having a melting point of 198°-200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666911 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-2fd9087da28744bb97d7896d2407f40e |
| Source note | uspto-grants-1987_05 |