反应详情

To a solution of ethyl 2-(5-acetamido-3-(4-fluorophenyl)-4-(phenylethynyl)-1H-pyrazol-1-yl)acetate (1 g, 2.5 mmol) in ethanol (40 mL) and methanol (10 ml) was added sodium borohydride (466 mg, 12.3 mmol and the reaction stirred at room temperature for 16 h. The reaction mixture was concentrated in vacuo and the residue was dissolved in CH2Cl2 and washed with a dilute NH4Cl solution. The aqueous was extracted with CH2Cl2 and the combined organic extracts were dried over MgSO4, filtered and evaporated. The crude product was suspended in CH2Cl2 (20 ml), heated to reflux, allowed to cool and the product was filtered and dried in vacuo to give N-(3-(4-fluorophenyl)-1-(2-hydroxyethyl)-4-(phenylethynyl)-1H-pyrazol-5-yl)acetamide as a white solid (659 mg), which was used as such in the subsequent step.

1. concentrationThe reaction mixture was concentrated in vacuo
2. dissolutionthe residue was dissolved in CH2Cl2
3. washwashed with a dilute NH4Cl solution
4. extractionThe aqueous was extracted with CH2Cl2
5. dry with materialthe combined organic extracts were dried over MgSO4
6. filtrationfiltered
7. customevaporated
8. temperatureheated
9. temperatureto reflux
10. temperatureto cool
11. filtrationthe product was filtered
12. customdried in vacuo