反应详情

温度

20 °C

In a 20-mL sealed tube was dissolved 4-(2-(4-(4-phenylphthalazin-1-ylamino)phenoxy)pyridin-3-yl)-1-H-pyrazole-3-carbonitrile (0.070 g, 0.145 mmol) in DMSO (1.0 mL). To this was added potassium carbonate (0.024 g, 0.174 mmol) and hydrogen peroxide (0.445 mL, 14.5 mmol) and the mixture was stirred at 20° C. for 3 days and quenched with water. The product was extracted into EtOAc, washed 1× saturated NaHCO3, 1×H2O, dried over Na2SO4, filtered through fritted funnel and concentrated. The title compound was purified using a Gilson reverse phase liquid chromatography system. The product fractions were extracted into CH2Cl2. The organic layers were washed organics 1× saturated NaHCO3, 1×H2O, dried with Na2SO4, filtered through fritted funnel and concentrated to yield 4-(2-(4-(4-phenylphthalazin-1-ylamino)phenoxy)pyridin-3-yl)-1-H-pyrazole-3-carboxamide as light yellow solid. MS m/z=500 [M+1]+. Calc'd for C29H21N7O2: 499.52.

1. customIn a 20-mL sealed tube
2. customquenched with water
3. extractionThe product was extracted into EtOAc
4. washwashed 1× saturated NaHCO3, 1×H2O
5. dry with materialdried over Na2SO4
6. filtrationfiltered through fritted funnel
7. concentrationconcentrated
8. customThe title compound was purified
9. extractionThe product fractions were extracted into CH2Cl2
10. washThe organic layers were washed organics 1× saturated NaHCO3, 1×H2O
11. dry with materialdried with Na2SO4
12. filtrationfiltered through fritted funnel
13. concentrationconcentrated