反応式
[CH3:1][C:2]1[CH:7]=[C:6]([S:8](=[O:11])(=[O:10])[NH2:9])[CH:5]=[CH:4][C:3]=1[NH:12][C:13]([C:15]1[CH:20]=[C:19](Cl)[N:18]=[CH:17][N:16]=1)=[O:14].[CH2:22]([NH:25][CH:26]([CH3:28])[CH3:27])[CH2:23][CH3:24]>>[NH2:9][S:8]([C:6]1[CH:5]=[CH:4][C:3]([NH:12][C:13]([C:15]2[CH:20]=[C:19]([N:25]([CH:26]([CH3:28])[CH3:27])[CH2:22][CH2:23][CH3:24])[N:18]=[CH:17][N:16]=2)=[O:14])=[C:2]([CH3:1])[CH:7]=1)(=[O:11])=[O:10]参加物
3
実験手順
Following the general method as outlined in Example 20, starting from 6-chloro-pyrimidine-4-carboxylic acid (2-methyl-4-sulfamoyl-phenyl)amide (Intermediate 17) and propyl-isopropylamine (Matrix), the title compound was obtained as a white solid.
出典と根拠
- ORDレコード
- ord-da86d518e5f949a9ac26f4b180ef861f
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08399448B2
関連ノート
読み込み中…