HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-(4-benzyloxycarbonylaminophenyl)-3-methyl-2(1H)-pyrazinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Pyrazine, 2-chloro-3-methyl- | HCID 66769 | — |
| Reactant | benzyl N-hydroxy-N-phenylcarbamate | HCID 12358018 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-benzyloxycarbonylaminophenyl)-3-methyl-2(1H)-pyrazinone | HCID 13853561 | — |
Reaction Steps
To a stirred suspension of sodium hydride (2.1 g, 50% in oil) in dry dimethylformamide (35 ml) with external cooling was added portionwise, benzyl N-hydroxy-N-phenylcarbamate (10.6 g). After 5 minutes a brown solution was obtained to which was added 2-chloro-3-methylpyrazine (5.5 g) and the mixture was allowed to attain room temperature. The solution was poured into water (200 ml) and the aqueous phase decanted from the dark oil. The aqueous solution deposited a yellow solid which was collected and washed with ethanol to give 5-(4-benzyloxycarbonylaminophenyl)-3-methyl-2(1H)-pyrazinone (1.55 g. m.p. 238°-240° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04556711 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-b3f42ff6bd44464ba312d37428adc2a6 |
| Source note | uspto-grants-1985_12 |