2-(7-bromo-5-methyl-1H-indol-3-yl)ethanamine hydrochloride → 6-Methyl-7-bromotryptamine hydrochloride

反応式

[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]2

参加物

反応物 2

HCID 164953872-(7-bromo-5-methyl-1H-indol-3-yl)ethanamine hydrochloride

HCID 70197338(2-Bromo-3-methylphenyl)hydrazine hydrochloride

生成物 1

HCID 187022556-Methyl-7-bromotryptamine hydrochloride

実験手順

6-Methyl-7-bromotryptamine hydrochloride was prepared (2.42 g) as described for 5-methyl-7-bromotryptamine hydrochloride in Example 4, except using 2-bromo-3-methylphenylhydrazine hydrochloride as starting material. ##STR35##

出典と根拠

ORDレコード: ord-b4078e8ddee246f38c406044b594f8a1
出典データセット: uspto-grants-1999_01
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US05861425

反応ノート

読み込み中…