反応式
[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2.[S:11]([C:15]1[CH:20]=[CH:19][C:18]([S:21](Cl)(=[O:23])=[O:22])=[CH:17][CH:16]=1)(=[O:14])(=[O:13])[NH2:12]>N1C=CC=CC=1>[NH:9]1[C:10]2[C:6](=[CH:5][CH:4]=[CH:3][C:2]=2[NH:1][S:21]([C:18]2[CH:17]=[CH:16][C:15]([S:11](=[O:14])(=[O:13])[NH2:12])=[CH:20][CH:19]=2)(=[O:23])=[O:22])[CH:7]=[CH:8]1参加物
実験手順
The synthesis of the present compound can be carried out according to the process disclosed in JP-A-7-165708. For example, the present compound can be synthesized as follows. After dissolving 264 mg (2 mmol) of 7-amino-1H-indole in pyridine, 767 mg (3 mmol) of 4-sulfamoylbenzenesulfonyl chloride is added thereto under stirring at room temperature. After the mixture is stirred overnight at room temperature, the solvent is evaporated under reduced pressure. Ethyl acetate and 0.2 N hydrochloric acid are added to the resulting residue. The organic layer is separated, washed with water, and dried over magnesium sulfate, followed by evaporation of the solvent. The resulting residue is purified by silica gel column chromatography to give 445 mg of N-(1H-indol-7-yl)-4-sulfamoylbenzenesulfonamide.
後処理
- customThe synthesis of the present compound
- additionis added
- stirringAfter the mixture is stirred overnight at room temperature
- customthe solvent is evaporated under reduced pressure
- additionEthyl acetate and 0.2 N hydrochloric acid are added to the resulting residue
- customThe organic layer is separated
- washwashed with water
- dry with materialdried over magnesium sulfate
- customfollowed by evaporation of the solvent
- customThe resulting residue is purified by silica gel column chromatography
出典と根拠
- ORDレコード
- ord-43a8760c721b4de49c9f488aa7441b9f
- 出典データセット
- uspto-grants-2000_05
- 特許番号
- US06060498
関連ノート
読み込み中…