تفاعل #792212

معادلة التفاعل

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

المذيبات

DMF

ظروف التفاعل

المعالجة

1. 1
   أخرىThe entire reaction mixture
2. 2
   تركيزwas then concentrated under reduced pressure
3. 3
   أخرىgave
4. 4
   أخرىan alkaline reaction (pH=9)
5. 5
   استخلاصthe mixture was extracted four times with ethyl acetate
6. 6
   تجفيفthe combined organic phases were dried with sodium sulfate
7. 7
   تركيزconcentrated under reduced pressure
8. 8
   أخرىThe residue was purified by chromatography on silica gel (mobile phase: cyclohexane/acetone)

الإجراء التجريبي

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.

المصدر