HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-3-bromo-5-methylpyrazine → 3-Methoxy-5-methyl-2-pyrazinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-3-bromo-5-methylpyrazine | HCID 9899043 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Methoxy-5-methyl-2-pyrazinamine | HCID 10701894 | 75% |
Reaction Steps
2-Amino-3-bromo-5-methylpyrazine (0.374 g) was added to a freshly prepared solution of sodium methoxide in methanol (made by addition of sodium (0.115 g) to methanol (6 ml)). The reaction was heated under reflux for 18 hours, cooled to ambient temperature and the solvent removed by evaporation. Water (5 ml) was added to the residue and extracted with dichloromethane (3×20 ml). The combined organic extracts were dried (MgSO4) and the solvent removed by evaporation. The residue was purified by chromatography on silica gel, eluting with dichloromethane to give 2-amino-3-methoxy-5-methylpyrazine as a white crystalline solid (0.208 g, 75%), m.p. 67°-69° C.; mass spectrum (+ve CI): 140 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861401 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-cb964fb0305349d4bd397da6bf4028e8 |
| Source note | uspto-grants-1999_01 |