HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596733Generated: October 25, 2026
Acetic Acid → 3-Methoxy-5-methylpyrazine-2-carboxamide
https://huagongshe.com/reaction/1596733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methylglyoxal | HCID 880 | — |
| Reactant | 2-Amino-2-cyanoacetamide | HCID 98341 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Methoxy-5-methylpyrazine-2-carboxamide | HCID 11062776 | 50% |
Reaction Steps
Under argon, 6 g (60.5 mmol) of 2-amino-2-cyanoacetamide was initially charged in 67 g of methanol. 1.67 g (9.3 mmol) of sodium methoxide solution (30%) was added and the mixture was stirred for at 20° C. 2 hours. After nuetralization with 0.558 g (9.3 mmol) of acetic acid, 11.55 g (64.1 mmol) of methylglyoxal solution (40%) was added. The mixture was stirred at 20° C. for 2 hours and then at 50° C. for 2 hours. The solvent was distilled off and the 3-methoxy-5-methylpyrazine-2-carboxamide was purified by column chromatography (eluent: ethyl acetate/methanol 4:1). This gave 5 g of 3-methoxy-5-methylpyrazine-2-carboxamide. The yield was 50 percent. Other data concerning the title product was:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06291674B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-dc871d675fd241ffa1958f90ccd2e7a4 |
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| Source note | uspto-grants-2001_09 |
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