2-(7-bromo-5-methyl-1H-indol-3-yl)ethanamine hydrochloride → 6-Methyl-7-bromotryptamine hydrochloride
Reaktionsgleichung
[ClH:1].C[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:15])[CH:4]=1.Cl.Br[C:18]1C(C)=CC=CC=1NN>>[ClH:1].[CH3:18][C:4]1[C:5]([Br:15])=[C:6]2[C:13](=[CH:14][CH:3]=1)[C:9]([CH2:10][CH2:11][NH2:12])=[CH:8][NH:7]2Komponenten
3
Versuchsvorschrift
6-Methyl-7-bromotryptamine hydrochloride was prepared (2.42 g) as described for 5-methyl-7-bromotryptamine hydrochloride in Example 7, except using 2-bromo-3-methylphenylhydrazine hydrochloride as starting material. ##STR43##
Quellen und Nachweise
- ORD-Eintrag
- ord-de143f91adb24f958b8ec10f61958388
- Quelldatensatz
- uspto-grants-1996_01
- Patentnummer
- US05488053
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