Reaktion #61798

ord-73b1284b5d64434fa84306f89f2d7488

Reaktionsgleichung

O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
OB(O)c1ccc(C(F)(F)F)cc1
4-(trifluoromethyl)phenyl boronic acid
COC(=O)c1cncc(Br)c1
methyl-5-bromo-pyridine-3-carboxylate
COC(=O)c1cncc(-c2ccc(C(F)(F)F)cc2)c1
5-(4-Trifluoromethyl-phenyl)-nicotinic acid methyl ester
Ausbeute 76.8%

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was cooled to room temperature
  2. 2
    Filtrationfiltered
  3. 3
    Sonstigethe filtrate evaporated
  4. 4
    Waschenwashed twice with water
  5. 5
    Trocknendried over sodium sulphate
  6. 6
    Sonstigeevaporated

Vorschrift

81 mg (0.07 mmol)Pd(PPh3)4 was added under argon at room temperature to a solution of 1.0 g (4.63 mmol) methyl-5-bromo-pyridine-3-carboxylate in 23 ml N,N-dimethylformamide and the mixture was heated to 80° C. Then 2.26 g (6.94 mmol) cesium carbonate and 0.97 g (5.09 mmol) of 4-(trifluoromethyl)phenyl boronic acid were added and the mixture was stirred at 80° C. over night. The reaction mixture was cooled to room temperature, filtered, and the filtrate evaporated. The residue was taken up with ethyl acetate, washed twice with water, dried over sodium sulphate and evaporated. Chromatography on silica (eluent: ethyl acetate/n-heptane 1:3) gave 1.0 g (68%) of 5-(4-Trifluoromethyl-phenyl)-nicotinic acid methyl ester

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07429605B2uspto-grants-2008_09