2-(7-bromo-5-methyl-1H-indol-3-yl)ethanamine hydrochloride → 4-Fluoro-5-methyltryptamine hydrochloride
反応式
[ClH:1].[CH3:2][C:3]1[CH:14]=[C:13]2[C:6]([NH:7][CH:8]=[C:9]2[CH2:10][CH2:11][NH2:12])=[C:5](Br)[CH:4]=1.Cl.[F:17]C1C=C(NN)C=CC=1C>>[ClH:1].[F:17][C:14]1[C:3]([CH3:2])=[CH:4][CH:5]=[C:6]2[C:13]=1[C:9]([CH2:10][CH2:11][NH2:12])=[CH:8][NH:7]2参加物
3
実験手順
4-Fluoro-5-methyltryptamine hydrochloride was prepared (2.20 g) as described for 5-methyl-7-bromotryptamine hydrochloride in Example 4, except using 3-fluoro-4-methylphenylhydrazine hydrochloride (6.00 g) as starting material.
出典と根拠
- ORDレコード
- ord-f4f686ff5da34437bca8c65bdff2cf4f
- 出典データセット
- uspto-grants-1998_01
- 特許番号
- US05705519
反応ノート
読み込み中…