反応式
[CH2:1]([N:3]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4]1)[CH3:2].[Cl-].[Cl:13][C:14]1[CH:23]=[CH:22][CH:21]=[C:20]([F:24])[C:15]=1[CH:16]=[N+:17]([CH3:19])[CH3:18].Cl[C:26]1[CH:33]=[CH:32][CH:31]=[C:30](F)[C:27]=1C=O.CNC>>[Cl:13][C:14]1[CH:23]=[CH:22][CH:21]=[C:20]([F:24])[C:15]=1[CH:16]([N:17]([CH3:19])[CH3:18])[C:5]1[C:6]2[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=2)[N:3]([CH2:1][CH3:2])[C:4]=1[C:26]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:27]=1参加物
5
実験手順
The preparation was carried out in accordance with general synthesis instructions 4 from 1-ethylindole and (2-chloro-6-fluoro-benzylidene)-dimethyl-ammonium chloride, which had been prepared in accordance with example 24 from 2-chloro-6-fluoro-benzaldehyde and dimethylamine.
出典と根拠
- ORDレコード
- ord-edbb3ab502d0484fa2274b7010e61a5c
- 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…