反応式
[CH3:1][O:2][C:3]1[CH:18]=[CH:17][C:6]([CH2:7][S:8][CH:9]2[CH:14]3[CH2:15][CH2:16][N:11]([CH2:12][CH2:13]3)[CH2:10]2)=[CH:5][CH:4]=1.[F:19][S:20]([O:23][CH3:24])(=[O:22])=[O:21]>C(Cl)Cl>[F:19][S:20]([O-:23])(=[O:22])=[O:21].[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][S:8][CH:9]2[CH:14]3[CH2:13][CH2:12][N+:11]([CH3:24])([CH2:16][CH2:15]3)[CH2:10]2)=[CH:17][CH:18]=1参加物
4
実験手順
The procedure described in preparation 6-(3) was repeated, but using 756 mg of 3-(4-methoxybenzylthio) quinuclidine and 271 μl of methyl fluorosulfonate in the presence of 5 ml of methylene chloride, to afford 1.078 g of the title compound as an oil.
後処理
- customThe procedure described in preparation 6-(3)
出典と根拠
- ORDレコード
- ord-d6f53c977c6a4da88b5af247b46a3d95
- 出典データセット
- uspto-grants-1992_04
- 特許番号
- US05104867
関連ノート
読み込み中…