4-Bromo-3-methylisoxazol-5-amine → 3-Chloro-2,5-dimethyl-N-(4-bromo-3-methyl-5-isoxazolyl)benzenesulfonamide
反応式
[NH2:1][C:2]1[O:6][N:5]=[C:4]([CH3:7])[C:3]=1[Br:8].[Cl:9][C:10]1[C:11]([CH3:21])=[C:12]([S:17](Cl)(=[O:19])=[O:18])[CH:13]=[C:14]([CH3:16])[CH:15]=1>>[Cl:9][C:10]1[C:11]([CH3:21])=[C:12]([S:17]([NH:1][C:2]2[O:6][N:5]=[C:4]([CH3:7])[C:3]=2[Br:8])(=[O:19])=[O:18])[CH:13]=[C:14]([CH3:16])[CH:15]=1参加物
3
実験手順
3-Chloro-2,5-dimethyl-N-(4-bromo-3-methyl-5-isoxazolyl)benzenesulfonamide was prepared from 5-amino-4-bromo-3-methylisoxazole and 3-chloro-2,5-dimethylbenzenesulfonyl chloride according to the procedures described in Example 30. The crude product was purified by recrystallization from ethyl acetate/hexanes to give a crystalline solid, m.p. 148-150° C., yield 71%.
後処理
- customThe crude product was purified by recrystallization from ethyl acetate/hexanes
- customto give a crystalline solid, m.p. 148-150° C., yield 71%