Reaktion #43413

ord-1f05eff2dd94404e9c600e754f9a6940

Reaktionsgleichung

O=S([O-])[O-].[Na+].[Na+]
sodium sulphite
[Na+].[O-]Cl
sodium hypochlorite
C=C(C)c1c(F)cnc2cc(F)c(OC)nc12
3,7-difluoro-8-(1-methylethenyl)-2-(methyloxy)-1,5-naphthyridine
O.O.O.O.O.O.O.[Ce+3].[Cl-].[Cl-].[Cl-]
cerium(III) chloride heptahydrate
C=C(CCl)c1c(F)cnc2cc(F)c(OC)nc12
8-[1-(Chloromethyl)ethenyl]-3,7-difluoro-2-(methyloxy)-1,5-naphthyridine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGAfter 15 minutes stirring the mixture
  2. 2
    Extraktionwas extracted with ether (3×200 ml)
  3. 3
    TrocknenThe combined organic extracts were dried over magnesium sulphate
  4. 4
    Sonstigeevaporated
  5. 5
    SonstigeThe residue was chromatographed on silica eluting a gradient of 0-50% ethyl acetate in hexane affording a white solid (320 mg, 34%)

Vorschrift

A solution of 3,7-difluoro-8-(1-methylethenyl)-2-(methyloxy)-1,5-naphthyridine (820 mg, 3.5 mmol) in tert-butanol (50 ml) under argon was treated with cerium(III) chloride heptahydrate (1.29 g, 3.5 mmol) followed by a solution of sodium hypochlorite (12% w/v, 2.6 ml, 4.2 mmol). After 30 minutes stirring, saturated aqueous sodium sulphite solution (20 ml) was added. After 15 minutes stirring the mixture was extracted with ether (3×200 ml). The combined organic extracts were dried over magnesium sulphate and evaporated. The residue was chromatographed on silica eluting a gradient of 0-50% ethyl acetate in hexane affording a white solid (320 mg, 34%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732460B2uspto-grants-2010_06