Reacción #792212

Ecuación de reacción

3-(1H-pyrazol-4-yl)pyridine

2-(6-bromopyridin-2-yl)pyrimidine

potassium carbonate

→

2-{6-[4-(Pyridin-3-yl)-1H-pyrazol-1-yl]pyridin-2-yl}pyrimidine

Disolventes

DMF

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe entire reaction mixture
2. 2
   Concentraciónwas then concentrated under reduced pressure
3. 3
   Otrogave
4. 4
   Otroan alkaline reaction (pH=9)
5. 5
   Extracciónthe mixture was extracted four times with ethyl acetate
6. 6
   Secadothe combined organic phases were dried with sodium sulfate
7. 7
   Concentraciónconcentrated under reduced pressure
8. 8
   OtroThe residue was purified by chromatography on silica gel (mobile phase: cyclohexane/acetone)

Procedimiento

DMF was added to 0.8 g (5.5 mmol) of 3-(1H-pyrazol-4-yl)pyridine (Angew. Chemie, 2006, 118 (8) 1304), 1.3 g (5.5 mmol) of 2-(6-bromopyridin-2-yl)pyrimidine (WO 2010/006713), 0.29 g (0.82 mmol) of copper-8-hydroxyquinoline complex (cf. Tetrahedron Lett, 2006, 149) and 2.28 g (16.5 mmol) of potassium carbonate, and the mixture was stirred at 120° C. under argon for 16 hours. The entire reaction mixture was then concentrated under reduced pressure. The residue was admixed with aqueous citric acid, aqueous sodium chloride, ethyl acetate and diluted aqueous sodium hydroxide solution until the mixture gave an alkaline reaction (pH=9), the mixture was extracted four times with ethyl acetate and the combined organic phases were dried with sodium sulfate and concentrated under reduced pressure. The residue was purified by chromatography on silica gel (mobile phase: cyclohexane/acetone). This gave 0.56 g (32% of theory) of 2-{6-[4-(pyridin-3-yl)-1H-pyrazol-1-yl]pyridin-2-yl}pyrimidine.

Fuente