Реакция #70907

Уравнение реакции

3-amino-6-(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine

3-Amino-6-(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine

isonicotinoyl chloride hydrochloride

→

title compound

Выход 68.0%

N-[6-(4-Fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]isonicotinamide

Выход 68.0%

Растворители

pyridine

Условия реакции

Обработка

1. 1
   workup.ADDITIONwere introduced under argon atmosphere
2. 2
   КонцентрированиеIt was concentrated
3. 3
   workup.DISSOLUTIONthe residue dissolved in a mixture of CHCl3 and 1 N HCl
4. 4
   ДругоеThe phases were separated
5. 5
   Экстракцияthe aqueous phase was extracted with CHCl3 (×2)
6. 6
   workup.ADDITIONThe aqueous phase was basified by slow addition of 1 N NaOH
7. 7
   workup.ADDITIONBrine was added
8. 8
   Экстракцияextracted with CHCl3 and EtOAc
9. 9
   СушкаThe organic phase was dried over Na2SO4
10. 10
    Концентрированиеconcentrated to dryness
11. 11
    ДругоеThe crude product obtained
12. 12
    Другоеwas purified by chromatography on silica gel
13. 13
    Температураof increasing polarity as eluent

Методика

In a volumetric flask, 3-amino-6-(4-fluorophenyl)-5-(4-pyridyl)-1H-pyrazolo[3,4-b]pyridine (0.20 g, 0.7 mmol, obtained in example 70), isonicotinoyl chloride hydrochloride (0.12 g, 0.7 mmol, obtained in section a) and pyridine (1 mL) were introduced under argon atmosphere. This was stirred at room temperature for 2 days. It was concentrated and the residue dissolved in a mixture of CHCl3 and 1 N HCl. The phases were separated and the aqueous phase was extracted with CHCl3 (×2). The aqueous phase was basified by slow addition of 1 N NaOH. Brine was added and extracted with CHCl3 and EtOAc. The organic phase was dried over Na2SO4 and concentrated to dryness. The crude product obtained was purified by chromatography on silica gel using CHCl3-MeOH mixtures of increasing polarity as eluent, to afford 98 mg of the title compound (yield: 68%).

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