HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 21701663, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | tert-Butyl piperazin-1-ylcarbamate | HCID 21701658 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21701663 | HCID 21701663 | — |
Reaction Steps
To a solution of N-(1-piperazinyl)-tert-butoxycarboxamide (15 g) in dichloromethane (200 ml) was added acetic anhydride (7.74 ml) and pyridine (6.63 ml). The mixture was stirred at ambient temperature for 1 hour. The solution was washed with saturated aqueous solution of sodium hydrogen carbonate and brine. The organic layer was collected, dried over magnesium sulfate, and concentrated. The residue was triturated with n-hexane to give N-(4-acetyl-1-piperazinyl)-tert-butoxycarboxamide (16.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06291464B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-7bfd8d3e7cd641c5bbe22ae679bd922f |
| Source note | uspto-grants-2001_09 |