Aluminium lithium hydride → 3-(1H-indol-2-yl)butan-1-amine
反応式
N1C2C(=CC=CC=2)C=C1CCCN.[NH:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[C:15]1[CH:23]([CH3:28])[CH2:24][C:25]([NH2:27])=O.[H-].[Al+3].[Li+].[H-].[H-].[H-]>>[NH:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[C:15]1[CH:23]([CH3:28])[CH2:24][CH2:25][NH2:27]参加物
4
実験手順
This compound was prepared in in the manner described above for (19a) using 3-indolyl-butyramide and lithium aluminum hydride. A 75% yield was obtained as a yellow solid: mp 51-53° C.
後処理
- customThis compound was prepared in in the manner
- customA 75% yield was obtained as a yellow solid
出典と根拠
- ORDレコード
- ord-a16917a4d9214c55ad7fa3a54f6cabc7
- 出典データセット
- uspto-grants-2000_09
- 特許番号
- US06121307
反応ノート
読み込み中…