反応式
[CH3:1][C:2]1[C:3]([N+:11]([O-:13])=[O:12])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([NH2:7])=[O:6].[F:14][B-:15]([F:18])([F:17])[F:16].[CH3:19][O+](C)C>ClCCl>[F:14][B-:15]([F:18])([F:17])[F:16].[CH3:1][C:2]1[C:3]([N+:11]([O-:13])=[O:12])=[C:4]([C:5](=[NH:7])[O:6][CH3:19])[CH:8]=[CH:9][CH:10]=1参加物
4
実験手順
To a solution of the title compound of Step A (1.07 g, 5.9 mmol) in dichloromethane (15 mL) was added trimethyloxonium tetrafluoroborate (1.06 g, 7.1 mmol) and the mixture was stirred overnight at ambient temperature. Concentration gave the title compound of Step B as a white solid (1.7 g).
後処理
- concentrationConcentration
出典と根拠
- ORDレコード
- ord-5d2eafe787294387a2a9834fa6d2e2b4
- 出典データセット
- uspto-grants-2008_05
- 特許番号
- US07375232B2
関連ノート
読み込み中…