反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]([S:10][CH3:11])=[N:7][C:6]=2[CH:12]=1.[C:13]1([CH3:24])[CH:18]=[CH:17][C:16]([S:19]([O:22]C)(=[O:21])=[O:20])=[CH:15][CH:14]=1>>[S:19]([C:16]1[CH:17]=[CH:18][C:13]([CH3:24])=[CH:14][CH:15]=1)([O-:22])(=[O:21])=[O:20].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]([S:10][CH3:11])=[N+:7]([CH3:13])[C:6]=2[CH:12]=1参加物
3
実験手順
5-Chloro-2-(Methylthio)benzothiazole (5.0 g, 0.023 mol) and 4.40 g methyl p-toluenesulfonate were heated to 152° C. for 7 minutes. Upon cooling, the mixture solidified and then was triturated with acetone to give 7.82 g (84%), mp 170°-185° C.
後処理
- temperatureUpon cooling
- customwas triturated with acetone
- customto give 7.82 g (84%), mp 170°-185° C.
出典と根拠
- ORDレコード
- ord-ccf7747bc7e0489c849ed2b64f55902a
- 出典データセット
- uspto-grants-1992_04
- 特許番号
- US05102781
関連ノート
読み込み中…