関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Pentyl nitrite | HCID 10026 | — |
| 反応物 | 18-Crown-6 | HCID 28557 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 反応物 | Methyl 4-amino-3-methylbenzoate | HCID 2736799 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Methyl 1-acetyl-1H-indazole-5-carboxylate | HCID 22591332 | 47.4% |
反応手順
To a stirred mixture of methyl 3-methyl-4-aminobenzoate (5.0 g, 30.0 mmol) and potassium acetate (2.94 g, 30.0 mmol) in chloroform (50 mL) is added acetic anhydride (5.66 mL, 60.0 mmol). The mixture is stirred for 30 min at rt, followed by the addition of 18-crown-6 (1.58 g, 6.0 mmol) and n-amyl nitrite (7.78 g, 66.0 mmol). The mixture is heated to reflux for 16 h, followed by cooling to rt. The mixture is washed sequentially with aqueous sodium bicarbonate solution (2×), water and brine. The organic layer is dried over MgSO4, filtered and concentrated in vacuo. The crude product is purified by flash chromatography on silica gel. Elution with hexanes-EtOAc (80:20) gives 3.1 g (47%) of methyl 1-acetyl-1H-indazole-5-carboxylate as a yellow solid: 1H NMR (400 MHz, CDCl3) δ 8.52-8.50, 8.3, 8.2, 4.0, 2.8.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06849620B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-6062662749034ec397236ef61309513e |
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| 出典メモ | uspto-grants-2005_02 |
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