참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Methylglyoxal | HCID 880 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 2-Aminomalononitrile 4-toluenesulfonate | HCID 18796971 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Methyl 3-methoxy-5-methylpyrazine-2-carboxylate | HCID 21702987 | 27% |
반응 단계
Under argon, 5 g (19.3 mmol) of 2-aminomalononitrile-4-toluenesulfonate was initially charged in 50 g of methanol. 4.09 g (22.7 mmol) of sodium methoxide solution (30%) was added and the mixture was stirred at 2° C. for 2 hours. After neutralization with 0.204 g (3.4 mmol) of acetic acid, 3.6 g (19.9 mmol) of methylglyoxal solution (40%) was added. The mixture was stirred at 40° C. for 2 hours and then, at 20° C., 9.2 g (80 mmol) of hydrochloric acid (32%) was added and the mixture was stirred at 20° C. for 6 hours. The solvent was distilled off and the methyl 3-methoxy-5-methylpyrazine-2-carboxylate was extracted with methylene chloride. This gave 1 g of methyl 3-methoxy-5-methylpyrazine-2-carboxylate. The yield was 27 percent. Other data concerning the title product was:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06066736 |
|---|
| 출처 데이터셋 | uspto-grants-2000_05 |
|---|
| ORD ID | ord-07967dd299cb4f2fbe524c8cbef10734 |
|---|
| 출처 메모 | uspto-grants-2000_05 |
|---|