反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8](Cl)(=[O:10])=[O:9])=[CH:4][C:3]=1[Cl:12].[NH:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1>C(Cl)Cl>[Cl:12][C:3]1[CH:4]=[C:5]([S:8]([N:13]2[CH2:18][CH2:17][O:16][CH2:15][CH2:14]2)(=[O:10])=[O:9])[CH:6]=[CH:7][C:2]=1[F:1]参加物
4
実験手順
4-fluoro-3-chlorobenzenesulphonyl chloride (0.9 g) was stirred in dry DCM (10 ml) and morpholine (0.69 ml) added. The mixture was allowed to stir at RT for 1 h and then quenched with water, extracted with DCM, dried (MgSO4) and evaporated under reduced pressure to give a white solid (1.10 g).
後処理
- customquenched with water
- extractionextracted with DCM
- dry with materialdried (MgSO4)
- customevaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-9630a25f50aa454dade9a9dfd6f7ac7e
- 出典データセット
- uspto-grants-2012_04
- 特許番号
- US08148572B2
関連ノート
読み込み中…