反応式
[C:1]1([C:7]2[NH:8][C:9]3[C:14]([CH:15]=2)=[CH:13][CH:12]=[CH:11][CH:10]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl-].[Cl:17][C:18]1[CH:27]=[CH:26][CH:25]=[C:24]([F:28])[C:19]=1[CH:20]=[N+:21]([CH3:23])[CH3:22].ClC1C=CC=C(F)C=1C=O.CNC>>[Cl:17][C:18]1[CH:27]=[CH:26][CH:25]=[C:24]([F:28])[C:19]=1[CH:20]([N:21]([CH3:23])[CH3:22])[C:15]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[NH:8][C:7]=1[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
5
実験手順
The preparation was carried out in accordance with general synthesis instructions 4 from 2-phenylindole 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-024ef80f0453487d912adea4ad07485b
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07091220B2
関連ノート
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