Reaktion #322949

ord-bc39318e70384a0c8e0c0f336d08e311

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe catalyst was filtered off
  2. 2
    Einengenthe filtrate was concentrated to half of the original volume
  3. 3
    EinengenThe aqueous concentrate
  4. 4
    Waschenwas washed three times with diethyl ether
  5. 5
    Sonstigeevaporated in vacuo
  6. 6
    workup.DISSOLUTIONThe residue was dissolved in water (25 ml)
  7. 7
    workup.ADDITIONpotassium chloride (1.25 g) was added
  8. 8
    SonstigeThe aqueous solution was chromatographed on non-ionic adsorption resin "Diaion HP-20 AG" (1.35×17.5 cm)
  9. 9
    Wascheneluting with water (100 ml) and 10% aqueous isopropyl alcohol (100 ml)

Vorschrift

A mixture of 4-nitrobenzyl (5R,6R)-6-[1-methyl-1-(4-nitrobenzyloxycarbonyloxy)ethyl]-3-(1-methyl-1H-tetrazol-5-ylthio)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (50 mg) and platinum (IV) oxide monohydrate (25 mg) in a mixture of dioxane (10 ml), ethanol (0.5 ml), 0.1M aqueous dipotassium hydrogen phosphate (2.35 ml) and water (3.5 ml) was shaken for an hour under a hydrogen atmosphere (40 psi) at ambient temperature. The catalyst was filtered off and the filtrate was concentrated to half of the original volume. The aqueous concentrate was washed three times with diethyl ether and evaporated in vacuo. The residue was dissolved in water (25 ml) and potassium chloride (1.25 g) was added thereto. The aqueous solution was chromatographed on non-ionic adsorption resin "Diaion HP-20 AG" (1.35×17.5 cm), eluting with water (100 ml) and 10% aqueous isopropyl alcohol (100 ml). The fractions, whose UV spectra showed λmax 289 nm, were combined and lyophilized to give potassium (5R,6R)-6-(1-hydroxy-1-methylethyl)-3-(1-methyl-1H-tetrazol-5-ylthio)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (17 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04640915uspto-grants-1987_02