HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → tert-Butyl pyrazin-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Di-(t-butoxycarbonyl)aminopyrazine | HCID 22014485 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl pyrazin-2-ylcarbamate | HCID 21992941 | 74.2% |
Reaction Steps
Di-(t-butoxycarbonyl)aminopyrazine (2.1 g, 7.1 mM) in methanol (50 ml) under nitrogen, was treated with aqueous sodium hydroxide (2.5 M, 2.84 ml, 7.1 mM), and stirred at ambient temperature for 2 hours. The mixture was neutralised by the addition of water (25 ml) and solid carbon dioxide, then methanol evaporated. The residual aqueous solution was extracted with dichloromethane (2×20 ml), the extracts washed with brine (20 ml) and evaporated. The resulting solid was triturated with isohexane (50 ml) to give the title product as a white solid (1.03 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087629B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-5ffcee3aef244c46ad73a59445cc6d99 |
| Source note | uspto-grants-2006_08 |