Methanol → 4-Methoxy-1H-pyrrolo[2,3-b]pyridine
反応式
Cl[C:2]1[CH:10]=[CH:9][N:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2.[OH-:11].[Na+].[CH3:13]O>>[CH3:13][O:11][C:2]1[CH:10]=[CH:9][N:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2参加物
4
実験手順
4-methoxy-7-azaindole 20 was prepared by reacting 4-chloro-7-azaindole 24 (prepared as described in Example 9) with sodium hydroxide in methanol as described by Girgis, N. et. al., J. Heterocyclic. Chem. 1989, 26:317-325.
出典と根拠
- ORDレコード
- ord-9f513d54f62048019550891dba4f8e52
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08461169B2
反応ノート
読み込み中…