反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.[Cl-].[CH3:12][O:13][C:14]1[CH:25]=[CH:24][CH:23]=[CH:22][C:15]=1[CH:16]=[N+:17]1[CH2:21][CH2:20][CH2:19][CH2:18]1>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH:16]([C:15]1[CH:22]=[CH:23][CH:24]=[CH:25][C:14]=1[O:13][CH3:12])[N:17]1[CH2:21][CH2:20][CH2:19][CH2:18]1参加物
3
実験手順
The preparation was carried out in accordance with general synthesis instructions 4 from 5-chloro-1H-indole and 1-(2-methoxy-benzylidene)-pyrrolidinium chloride, which had been prepared in accordance with example 24.
後処理
- customhad been prepared in accordance with example 24
出典と根拠
- ORDレコード
- ord-caea7a624f0243c3b2e28a344715d0ec
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07091220B2
関連ノート
読み込み中…