참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl 3-aminopyrazinecarboxylate | HCID 72669 | — |
| 반응물 | N-Iodosuccinimide | HCID 120273 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Methyl 3-amino-6-iodopyrazine-2-carboxylate | HCID 11087124 | 88% |
반응 단계
1.5 equivalents of N-iodosuccinimide are added at room temperature to 5 g (32.7 mmol) of a methyl 3-aminopyrazine-2-carboxylate solution in 25 ml of dimethylformamide. The reaction medium is heated at 65° C. for 1 hour, added together with 0.5 equivalents of N-iodosuccinimide and maintained at 65° C. for 24 hours. After returning to room temperature, the solvent is evaporated and then the product is extracted several times with dichloromethane. The organic phases are combined, washed with 10% sodium bisulfite solution, dried on magnesium sulfate and concentrated to yield 8 g (88%) of methyl 3-amino-6-iodopyrazine-2-carboxylate in the form of a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09381195B2 |
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| 출처 데이터셋 | uspto-grants-2016_07 |
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| ORD ID | ord-595a4a987c054d4fa6209b857f337209 |
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| 출처 메모 | uspto-grants-2016_07 |
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