Acetonitrile → benzhydryl 7-amino-3-[(Z)-2-(3-pyridyl)vinylthio]-3-cephem-4-carboxylate
反応式
[NH2:1][CH:2]1[C:30](=[O:31])[N:4]2[C:5]([C:14]([O:16][CH:17]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[O:15])=[C:6](OS(C)(=O)=O)[CH2:7][S:8][C@H:3]12.C[Si](N[C:37]([NH:39][Si](C)(C)C)=O)(C)C.[C:44](#N)[CH3:45]>>[NH2:1][CH:2]1[C:30](=[O:31])[N:4]2[C:5]([C:14]([O:16][CH:17]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)=[O:15])=[C:6]([S:8]/[CH:7]=[CH:6]\[C:5]3[CH:14]=[N:39][CH:37]=[CH:45][CH:44]=3)[CH2:7][S:8][C@H:3]12参加物
4
実験手順
The mixture was stirred for 30 minutes. To the mixture was added a solution of benzhydryl 7-amino-3-mesyloxy-3-cephem-4-carboxylate (9.21 g) and bis-(trimethylsilyl)urea (12.26 g) in acetonitrile (276 ml) under ice-cooling. The reaction mixture was stirred for 10 minutes at the same temperature. The insoluble material was filtered off. The filtrate was concentrated in vacuo and the residue was dissolved in ethyl acetate. The ethyl acetate solution was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo to give benzhydryl 7-amino-3-[(Z)-2-(3-pyridyl)vinylthio]-3-cephem-4-carboxylate (6.17 g).
後処理
- temperaturecooling
- stirringThe reaction mixture was stirred for 10 minutes at the same temperature
- filtrationThe insoluble material was filtered off
- concentrationThe filtrate was concentrated in vacuo
- dissolutionthe residue was dissolved in ethyl acetate
- washThe ethyl acetate solution was washed with water and brine
- dry with materialdried over magnesium sulfate
- customevaporated in vacuo
出典と根拠
- ORDレコード
- ord-28f01401d39e466cb67a7457e858887a
- 出典データセット
- uspto-grants-1989_10
- 特許番号
- US04871730
反応ノート
読み込み中…