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

HRID 2351141Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2351141
[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

Komponenten

4

Versuchsvorschrift

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).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-28f01401d39e466cb67a7457e858887a
Quelldatensatz
uspto-grants-1989_10
Patentnummer
US04871730

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