5-Azaindole → 3-Chloro-1H-pyrrolo[3,2-c]pyridine
反応式
[NH:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[CH:2]1.[Cl:10]N1C(=O)CCC1=O>ClCCl>[Cl:10][C:3]1[C:4]2[CH:5]=[N:6][CH:7]=[CH:8][C:9]=2[NH:1][CH:2]=1参加物
4
実験手順
A solution of 1H-pyrrolo[3,2-c]pyridine (200 mg, 1.69 mmol) in dichloromethane (10 ml) was treated with N-chlorosuccinimide (339 mg, 2.5 mmol) and stirred at room temperature for 5 hours. The reaction mixture was diluted with dichloromethane and washed with aqueous sodium hydrogen carbonate solution, brine, dried over anhydrous sodium sulfate and concentrated. Purification from silica gel column chromatography using methanol and dichloromethane gradient afforded 3-chloro-1H-pyrrolo[3,2-c]pyridine (98 mg, 40%).
後処理
- washwashed with aqueous sodium hydrogen carbonate solution, brine
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated
- customPurification from silica gel column chromatography
出典と根拠
- ORDレコード
- ord-33c1d451262c4cfea337a15c8de83587
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08980911B2
反応ノート
読み込み中…