4-(4-Chloro-3-dimethylsulfamoylphenyl)-3-methyl-2-(2,4-dimethylphenyl-imino)thiazolidin-4-ol hydrobromide → 4-(4-Chloro-3-dimethylsulfamoylphenyl)-3-methyl-2-(2,4-dimethylphenyl-imino)-4-thiazoline hydrobromide
反応式
[BrH:1].[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2(O)[CH2:13][S:12][C:11](=[N:14][C:15]3[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][C:16]=3[CH3:22])[N:10]2[CH3:23])=[CH:5][C:4]=1[S:25](=[O:30])(=[O:29])[N:26]([CH3:28])[CH3:27]>C(O)(=O)C>[BrH:1].[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:10]([CH3:23])[C:11](=[N:14][C:15]3[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][C:16]=3[CH3:22])[S:12][CH:13]=2)=[CH:5][C:4]=1[S:25](=[O:30])(=[O:29])[N:26]([CH3:28])[CH3:27]参加物
3
実験手順
Obtained by a procedure analogous to that indicated in Example 1 (b), from 4-(4-chloro-3-dimethylsulfamoylphenyl)-3-methyl-2-(2,4-dimethylphenyl-imino)thiazolidin-4-ol hydrobromide. Colorless crystals; melting point 264° C. (from glacial acetic acid).