反応式
[C:1]1(=[O:11])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][NH:2]1.[Cl:12][S:13](O)(=[O:15])=[O:14]>>[O:11]=[C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([S:13]([Cl:12])(=[O:15])=[O:14])[CH:9]=2)[CH2:4][CH2:3][NH:2]1参加物
3
実験手順
To Chlorosulfonic acid (30 mL) is added 3,4-Dihydro-2H-isoquinolin-1-one (5 g, 34 mmol) at 0° C. After stirring at rt during 1 h, the mixture is heated at 50° C. during 16 h, then it is poured carefully into an ice bath and stirred at 0° C. during 30 min. The precipitate is filtered and dried in oven at 60° C. to give the title compound.
後処理
- temperaturethe mixture is heated at 50° C. during 16 h
- additionit is poured carefully into an ice bath
- stirringstirred at 0° C. during 30 min
- filtrationThe precipitate is filtered
- customdried in oven at 60° C.
出典と根拠
- ORDレコード
- ord-0cdbec0b6c6740fdb45be0f8d044b403
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07888351B2
関連ノート
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