Reaktion #48600

ord-abb1c6f593064b278921ff370239f3b1

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethen evaporated under reduced pressure
  2. 2
    SonstigeThe residue was partitioned between ethyl acetate and brine
  3. 3
    Sonstigethe ethyl acetate layer was separated
  4. 4
    Trocknendried (MgSO4)
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigeevaporated
  7. 7
    SonstigeThe crude material was purified by flash column chromatography
  8. 8
    Wascheneluting with 1:3 ethyl acetate/hexane
  9. 9
    workup.ADDITIONthe product containing fractions
  10. 10
    Sonstigeevaporated

Vorschrift

A solution of 4-iodo-1H-pyrazole-3-carboxylic acid phenylamide (670 mg; 2.14 mmol) in acetonitrile (10 ml) was treated with potassium carbonate (360 mg; 2.57 mmol)) followed by 4-methoxybenzyl chloride (320 μl; 2.35 mmol). The mixture was stirred at room temperature overnight then evaporated under reduced pressure. The residue was partitioned between ethyl acetate and brine; the ethyl acetate layer was separated, dried (MgSO4), filtered and evaporated. The crude material was purified by flash column chromatography eluting with 1:3 ethyl acetate/hexane and the product containing fractions combined and evaporated to give 660 mg of 4-iodo-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745638B2uspto-grants-2010_06