関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 反応物 | Mucobromic Acid | HCID 3033972 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | Propionimidamide hydrochloride | HCID 12301253 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-Bromo-2-ethylpyrimidine-4-carboxylic acid | HCID 66977702 | 37% |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08461157B2 |
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| 出典データセット | uspto-grants-2013_06 |
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| ORD ID | ord-50672b3b031641a89651b56c4c1cebcc |
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| 出典メモ | uspto-grants-2013_06 |
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