Potassium Hydroxide → 5-Bromo-3-iodo-1H-pyrrolo(2,3-b)pyridine
反応式
[Br:1][C:2]1[CH:3]=[C:4]2[CH:10]=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1.[OH-].[K+].[I:13]N1C(=O)CCC1=O.[O-]S([O-])(=S)=O.[Na+].[Na+]>C(Cl)Cl>[I:13][C:10]1[C:4]2[C:5](=[N:6][CH:7]=[C:2]([Br:1])[CH:3]=2)[NH:8][CH:9]=1参加物
6
実験手順
To a solution of 5-bromo-1H-pyrrolo[2,3-b]-pyridine (commercial product, 1 g, 5.10 mmol) in 200 ml of CH2Cl2 is added KOH (145 mg, 2.55 mmol) at room temperature. After 30 minutes, N-iodosuccinimide (1.2 g, 5.10 mmol) is added and the solution is stirred for 15 hours, neutralized with saturated Na2S2O3 solution and extracted several times with CH2Cl2. The organic phases are combined, dried on MgSO4 and concentrated under reduced pressure. The expected product is obtained with a quantitative yield and used in the following step without additional purification.
後処理
- extractionextracted several times with CH2Cl2
- customdried on MgSO4
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-96d829c812d74501a86acdbdb74a4796
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09447093B2
反応ノート
読み込み中…