反応式
Br[C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([CH3:9])[CH:3]=1.B([C:13]1[CH:21]=[CH:20][C:16]([C:17]([OH:19])=[O:18])=[CH:15][C:14]=1[CH3:22])(O)O>>[NH2:6][C:5]1[CH:7]=[CH:8][C:2]([C:13]2[CH:21]=[CH:20][C:16]([C:17]([OH:19])=[O:18])=[CH:15][C:14]=2[CH3:22])=[CH:3][C:4]=1[CH3:9]参加物
3
実験手順
The title compound was prepared from 4-bromo-2-methylaniline and 4-borono-3-methylbenzoic acid (D29) using a similar procedure to Description 1 as a brown solid (41%). This was used in the next step without further purification.
後処理
- customThis was used in the next step without further purification
出典と根拠
- ORDレコード
- ord-3834fa6b35b140f99b470d78d13eaf95
- 出典データセット
- uspto-grants-2000_08
- 特許番号
- US06100272
関連ノート
読み込み中…