反応式
[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[N:5][N:6]2C(=O)C.Cl>CO>[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[N:5][NH:6]2参加物
4
実験手順
To a solution of the 1-(4-bromo-indazol-1-yl)-ethanone A (3.09 g, 12.9 mmol) in MeOH (50 mL) was added 6N aqueous HCl (30 mL) and the mixture was stirred at room temperature for 7 h. The MeOH was evaporated and the mixture partitioned between EtOAc (2×50 mL) and water (50 mL). The combined organic layers were washed with brine (50 mL), separated and dried (MgSO4). The solvent was removed by evaporation under reduced pressure to give 4-bromo-1H-indazole B (2.36 g, 93%).
後処理
- customThe MeOH was evaporated
- customthe mixture partitioned between EtOAc (2×50 mL) and water (50 mL)
- washThe combined organic layers were washed with brine (50 mL)
- customseparated
- dry with materialdried (MgSO4)
- customThe solvent was removed by evaporation under reduced pressure
出典と根拠
- ORDレコード
- ord-0dbc0e1b6ef84b0882b268426ec4a69b
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09346817B2
関連ノート
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