Reaktion #11878
ord-1bfc78b0e9c34df2912beabf6aeef46e
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1WaschenThe reaction mixture was washed with hexanes (50 mL×3)
- 2Sonstigethe supernatant was decanted off after each time
- 3workup.DISSOLUTIONThe residue was dissolved in ethyl acetate (100 mL)
- 4Waschensuccessively washed with saturated aqueous ammonium chloride solution (30 mL), water (30 mL) and brine (30 mL)
- 5Trocknendried over anhydrous sodium sulfate
- 6Filtrationfiltered
- 7Einengenconcentrated in vacuo
- 8SonstigeThe crude product was then triturated with ethyl acetate-hexanes
- 9FiltrationThe resulting solid was collected by filtration
- 10Waschenwashed with diethyl ether
Vorschrift
A mixture of 2-(3,5-bis-trifluoromethyl-phenyl)-3-(2,4-dichloro-pyrimidin-5-yl)-propionic acid methyl ester (0.35 g, 0.78 mmol) (from Example 8b supra) and aniline (2.0 mL) (Aldrich) was heated at 120° C. for 1 hour. The reaction mixture was washed with hexanes (50 mL×3) and the supernatant was decanted off after each time. The residue was dissolved in ethyl acetate (100 mL) and successively washed with saturated aqueous ammonium chloride solution (30 mL), water (30 mL) and brine (30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The crude product was then triturated with ethyl acetate-hexanes. The resulting solid was collected by filtration and washed with diethyl ether to give crude 3-(2,4-diphenylamino-pyrimidin-5-yl)-2-(3,5-bis-trifluoromethyl-phenyl)-propionic acid methyl ester as an off-white solid which was used in the next step without further purification. (Yield 0.47 g).