Potassium Hydroxide → 6-(dimethylamino)-1H-indole-2-carboxylic acid
反応式
[CH3:1][N:2]([C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]([O:15]C)=[O:14])[NH:10]2)=[CH:6][CH:5]=1)[CH3:3].[OH-].[K+]>>[CH3:3][N:2]([C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]([OH:15])=[O:14])[NH:10]2)=[CH:6][CH:5]=1)[CH3:1]参加物
3
実験手順
Following the general procedure of PREPARATION 63 and making non-critical variations but starting with methyl 6-(N,N-dimethylamino)indole-2-carboxylate (PREPARATION 88, 0.80 g), potassium hydroxide (0.25 g), the title compound is obtained, NMR (300 MHz, CD3OD) 7.62, 7.13, 7.11, 7.01, and 3.11 δ.
後処理
- customthe general procedure of PREPARATION 63
出典と根拠
- ORDレコード
- ord-351f068d2c5e4e2981f62b7c7d8a2302
- 出典データセット
- uspto-grants-1996_10
- 特許番号
- US05563142
反応ノート
読み込み中…