HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → Ethyl 2-(3-bromo-6-methyl-2-oxopyrazin-1(2H)-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | HCID 178472615 | HCID 178472615 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 2-(3-bromo-6-methyl-2-oxopyrazin-1(2H)-yl)acetate | HCID 1514288 | — |
Reaction Steps
A stirred slurry of 505 mg (2.38 mmol) of 1-(ethoxycarbonyl-methyl)-3-hydroxy-6-methylpyrazinone and 756 mg (2.64 mmol) of phosphorous oxybromide in 1.7 ml of CHCl3 was stirred at 50° C. under a slow stream of Ar for 1.5 h, then allowed to cool to rt overnight. The reaction mixture was diluted with CHCl3 and ice water, basified with NH4OH, and extracted with CHCl3. The combined organic layers were dried over Na2SO4, treated with activated carbon, filtered and concentrated to give 2-5 as an orange colored solid: 1H NMR (CDCl3) δ7.06 (s, 1H), 4.77 (s, 2H), 4.27 (q, 2H, 7.2 Hz), 2.24 (s, 3H), 1.31 (t, 3H, 7.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06462050B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-fce419494014425188b09ebe29bceaba |
| Source note | uspto-grants-2002_10 |