HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-Bromoacetamide → 1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-methylsulfonyl-2-azetidinone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-Bromoacetamide | HCID 4353 | — |
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | Sodium Thiosulfate | HCID 24477 | — |
| Edukt | 1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-(methylthio)-2-azetidinone | HCID 86737252 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-methylsulfonyl-2-azetidinone | HCID 86737251 | — |
Reaktionsschritte
1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-(methylthio)-2-azetidinone (0.44 g.) is dissolved in methanol (20 ml.) and treated with N-bromoacetamide (0.52 g.) for two hours. Sodium thiosulfate (10 ml.; 0.1N) is then added and the mixture is allowed to stir for five minutes. At the end of this time, the reaction mixture shows no positive reaction to starch iodide paper. The reaction mixture is saturated with sodium chloride and extracted with methylene chloride. The methylene chloride extract is dried and evaporated. The residue is chromatographed to afford 1-(benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-methylsulfonyl-2-azetidinone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04957912 |
| Quelldatensatz | uspto-grants-1990_09 |
| ORD ID | ord-428b98e828e94a269771bea05d804bbe |
| Quellennotiz | uspto-grants-1990_09 |