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Potassium Hydroxide → 3-Bromo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 4-Nitroindazole | HCID 18057 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 6-Chloromethyl-2-methylpyridinium chloride | HCID 76545 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-Bromo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole | HCID 67259864 | 80.3% |
反応手順
4-Nitro-1H-indazole (1.0 g, 6.1 mmol) and N-bromosuccinimide (1.1 g, 6.4 mmol) were mixed with anhydrous DMF (10 mL) in a 20 mL vial. The reaction was stirred at ambient temperature for 5 minutes. KOH (1.1 g, 18.3 mmol) and 2-(chloromethyl)-6-methylpyridine hydrochloride (1.4 g, 7.6 mmol) were added to the vial and the reaction mixture was stirred for 18 hours. The product was precipitated from solution by addition of H2O (10 mL) to the reaction mixture. The solids were collected vacuum filtration, washed with H2O and dried under vacuum to afford 3-bromo-1-((6-methylpyridin-2-yl)methyl)-4-nitro-1H-indazole (1.7 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08841455B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-dcb6ec09e098432b8505ca359813cc51 |
| 出典メモ | uspto-grants-2014_09 |