反応式
F[C:2]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[S:15]([NH2:18])(=[O:17])=[O:16])[CH:6]=[CH:5][C:3]=1[NH2:4].[CH3:19]C1C=C(Br)C=CC=1N.FC1C=C(Br)C=CC=1N>>[CH3:19][C:2]1[CH:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[S:15]([NH2:18])(=[O:17])=[O:16])[CH:6]=[CH:5][C:3]=1[NH2:4]参加物
4
実験手順
This compound was prepared by the method described for 2-fluoro-4-(2-aminosulfonylphenyl)aniline described in EXAMPLE 8 by starting with 2-methyl-4-bromoaniline rather than 2-fluoro-4-bromoaniline.
後処理
- customThis compound was prepared by the method
出典と根拠
- ORDレコード
- ord-d05acb640ff64d9e8cd8fc67f549f565
- 出典データセット
- uspto-grants-2002_06
- 特許番号
- US06403620B1
関連ノート
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