Acetonitrile → benzhydryl 7-amino-3-[(Z)-2-(3-pyridyl)vinylthio]-3-cephem-4-carboxylate

HRID 2351141ノート

反応式

HRID 2351141 の反応式
[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

  1. temperaturecooling
  2. stirringThe reaction mixture was stirred for 10 minutes at the same temperature
  3. filtrationThe insoluble material was filtered off
  4. concentrationThe filtrate was concentrated in vacuo
  5. dissolutionthe residue was dissolved in ethyl acetate
  6. washThe ethyl acetate solution was washed with water and brine
  7. dry with materialdried over magnesium sulfate
  8. 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

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