2,4-Difluoroaniline → 2,4-Difluoro-N-(4-sulfamoylbenzylidene)aniline
反応式
[S:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=O)=[CH:7][CH:6]=1)(=[O:4])(=[O:3])[NH2:2].[F:13][C:14]1[CH:20]=[C:19]([F:21])[CH:18]=[CH:17][C:15]=1[NH2:16]>>[F:13][C:14]1[CH:20]=[C:19]([F:21])[CH:18]=[CH:17][C:15]=1[N:16]=[CH:9][C:8]1[CH:11]=[CH:12][C:5]([S:1](=[O:4])(=[O:3])[NH2:2])=[CH:6][CH:7]=1参加物
3
実験手順
Following a procedure similar to that described in Example 1(i), but using 4-sulfamoylbenzaldehyde and 2,4-difluoroaniline as starting materials, the title compound was obtained as a white powder (yield 47%).
出典と根拠
- ORDレコード
- ord-14c331b86cf94667b413c9b53c779491
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- USRE039420E1
反応ノート
読み込み中…