HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → N-methylpiperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Product | N-methylpiperazine-1-carboxamide | HCID 11672770 | — |
Reaction Steps
To the solution of piperazine (3 g) in dichloromethane (30 ml) was addedmethyl isocyanate (2.16 ml) in an ice water bath with stirring. After 10 minutes the mixture was stirred at ambient temperature for 1 hour. The reaction mixture was evaporated in vacuo. The residue was diluted with acetonitrile (15 ml) and crystals were filtered off. The filtrate was evaporated in vacuo. To the residue was added xylene and the solvent was azeotropically removed in vacuo to give N-methyl-1-piperazinecarboxamide (2.43 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06169095A |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-9eb280ed21d84f68806555f2a725ea1d |
| Source note | uspto-grants-2001_01 |