Sodium Hydroxide → 1H-Pyrrolo[2,3-b]pyridine, 6-chloro-2-Methyl-
反応式
COC([N:5]1[C:9]2=[N:10][C:11]([Cl:14])=[CH:12][CH:13]=[C:8]2[CH:7]=[C:6]1[CH3:15])=O.[OH-].[Na+]>CO>[Cl:14][C:11]1[N:10]=[C:9]2[NH:5][C:6]([CH3:15])=[CH:7][C:8]2=[CH:13][CH:12]=1参加物
4
実験手順
6-Chloro-2-methyl-pyrrolo[2,3-b]pyridine-1-carboxylic acid methyl ester (0.225 g, 1 mmol) is dissolved in methanol (30 ml) and 1M NaOH (10 ml) and stirred at room temperature overnight. The methanol is removed in vacuo and the resulting white suspension is extracted with chloroform (3×20 ml), dried (MgSO4) and concentrated in vacuo to yield a white powder which is dried under high vacuum to yield the titled product. (MH+ 167).
後処理
- customThe methanol is removed in vacuo
- extractionthe resulting white suspension is extracted with chloroform (3×20 ml)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customto yield a white powder which
- customis dried under high vacuum
出典と根拠
- ORDレコード
- ord-4460029ef2f7407d806a045a5e408d54
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08791256B2
反応ノート
読み込み中…