참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | Mucobromic Acid | HCID 3033972 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | Propionimidamide hydrochloride | HCID 12301253 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 5-Bromo-2-ethylpyrimidine-4-carboxylic acid | HCID 66977702 | 37% |
반응 단계
Sodium (356 mg, 15.5 mmol) was carefully added to ethanol (5.9 mL) to prepare sodium ethoxide solution in ethanol. The above freshly prepared ethanol solution (3.5 mL) was added to a stirred suspension of propionimidamide hydrochloride (1.05 g, 9.69 mmol). The mixture was warmed to 55° C., then the heating bath was removed and a solution of mucobromic acid (1 g, 3.87 mmol) in ethanol was added dropwise at a rate which maintained a constant temperature, followed by a further sodium ethoxide solution (2 mL). After cooling, the mixture was filtered and evaporated to a residue which was shaken vigorously with hydrochloric acid (2 M×2.4 mL). The brown precipitate was filtered off and washed with cold water, then freeze-dried to give 5-Bromo-2-ethylpyrimidine-4-carboxylic acid (330 mg, 37%) as a yellow solid. LCMS: 231 [M+1]+, 1H NMR (400 MHz, DMSO-d6): δ 1.25 (t, J=7.6 Hz, 3H), 2.88 (q, J=7.6 Hz, 2H), 9.05 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08461157B2 |
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| 출처 데이터셋 | uspto-grants-2013_06 |
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| ORD ID | ord-50672b3b031641a89651b56c4c1cebcc |
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| 출처 메모 | uspto-grants-2013_06 |
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