Reaktion #45877

ord-aa631540665a49e59cd3384132a16db5

Reaktionsgleichung

Cc1c(Br)c(F)c(O)c(N)c1C#N
2-Amino-5-bromo-4-fluoro-3-hydroxy-6-methylbenzonitrile
OB(O)c1cccc(Cl)c1
3-chlorophenylboronic acid
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CC1(C#N)CC(c2cccc(Cl)c2)=C(F)C(O)=C1N
compound
Ausbeute 78.0%
CC1(C#N)CC(c2cccc(Cl)c2)=C(F)C(O)=C1N
4-Amino-3′-chloro-6-fluoro-5-hydroxy-3-methylbiphenyl-3-carbonitrile
Ausbeute 78.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter cooling to room temperature
  2. 2
    Sonstigethe insoluble matter was separated by filtration
  3. 3
    Waschenwith washing with ethyl acetate
  4. 4
    EinengenThe filtrate was concentrated under reduced pressure
  5. 5
    SonstigeThe aqueous layer was separated
  6. 6
    Extraktionthis was further extracted twice with ethyl acetate
  7. 7
    Waschenwashed with saturated brine
  8. 8
    Trocknendried over anhydrous sodium sulfate
  9. 9
    SonstigeThe insoluble matter was separated by filtration
  10. 10
    Sonstigethe solvent was evaporated away
  11. 11
    Sonstigethe resulting residue was purified by middle-pressure liquid chromatography (eluent, chloroform

Vorschrift

2-Amino-5-bromo-4-fluoro-3-hydroxy-6-methylbenzonitrile (I-75) (2.0 g, 8.16 mmol), 3-chlorophenylboronic acid (2.63 g, 16.3 mmol) and cesium carbonate (5.32 g, 16.3 mmol) were dissolved in 1,4-dioxane (90 ml)/water (10 ml), and at room temperature, (tetrakistriphenylphosphine)palladium(0) (943 mg, 0.82 mmol) was added. The solution was stirred in a nitrogen steam at 100° C. for 12 hours. After cooling to room temperature, the insoluble matter was separated by filtration with washing with ethyl acetate. The filtrate was concentrated under reduced pressure, and the residue was fractionated with ethyl acetate and saturated brine. The aqueous layer was separated, this was further extracted twice with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, chloroform:ethyl acetate=95:5, v/v) to obtain the entitled compound (1.76 g, 78%) as a pale brown solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737166B2uspto-grants-2010_06