참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 5-Bromonicotinamide | HCID 1808 | — |
| 용매 | Phosphorus oxychloride | HCID 24813 | — |
| 생성물 | 5-Bromonicotinonitrile | HCID 736793 | 70% |
반응 단계
5-Bromo-3-pyridinylcarboxamide (10 g, 49.7 mmol) in phosphorus oxychloride (25 mL) was warmed to reflux for 18 h, allowed to cool to 25° C., concentrated in vacuo and carefully treated with satd. aqueous sodium bicarbonate (˜500 mL) until neutralized. The reaction mixture was diluted with CH2Cl2 (200 mL), stirred for 4 h, and the layers were separated. The aqueous layer was washed with CH2Cl2 (2×100 mL), and the organic layers were combined and dried (MgSO4). The resulting solution was concentrated in vacuo to afford the title compound (6.35 g, 70%) as a white solid. MS 184 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713455B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-30c79bf012b64918808d4c344a0bd047 |
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| 출처 메모 | uspto-grants-2004_03 |
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