反应详情

温度

100 °C

A suspension of 3-acetyl-1-[2-fluoro-4-(1H-pyrazol-1-yl)phenyl]-5-methoxypyridazin-4(1H)-one (393 mg, 1.20 mmol) in N,N-dimethylformamide dimethyl acetal (4.0 mL) was stirred at 100° C. for 1 h. The reaction mixture was concentrated in vacuo. To the residue were added AcOH (4 mL) and 3-chlorophenylhydrazine hydrochloride (429 mg, 2.40 mmol). The mixture was stirred at 100° C. for 1 h. After solvent evaporated, the residue was diluted with saturated NaHCO3 aqueous solution (25 mL) and extracted with AcOEt (25 mL×3). The combined organic phase was washed with brine (40 mL), dried with MgSO4, and evaporated. The residue was crystallized from AcOEt to give a coarse solid, which was recrystallized from EtOH/hexane to give the title compound (242 mg, 44% yield) as an orange solid: mp 186-190° C.; 1H NMR (300 MHz, DMSO-d6): δ ppm 3.80 (3H, s), 6.64 (1H, d, J=1.9 Hz), 7.05 (1H, d, J=1.9 Hz), 7.27-7.34 (1H, m), 7.44 (3H, dd, J=16.6, 10.2 Hz), 7.34-7.52 (1H, m), 7.84 (3H, dd, J=3.6, 1.7 Hz), 8.00 (1H, dd, J=12.3, 2.1 Hz), 8.56 (1H, d, J=1.9 Hz), 8.67 (1H, d, J=2.6 Hz): LC-MS (ESI) m/z 463 [M+H]+. Anal. Calcd for C23H16ClFN6O2.0.03H2O: C, 59.61; H, 3.49; N, 18.14. Found: C, 59.32; H, 3.50; N, 17.92.

1. concentrationThe reaction mixture was concentrated in vacuo
2. stirringThe mixture was stirred at 100° C. for 1 h
3. customAfter solvent evaporated
4. additionthe residue was diluted with saturated NaHCO3 aqueous solution (25 mL)
5. extractionextracted with AcOEt (25 mL×3)
6. washThe combined organic phase was washed with brine (40 mL)
7. dry with materialdried with MgSO4
8. customevaporated
9. customThe residue was crystallized from AcOEt
10. customto give a coarse solid, which
11. customwas recrystallized from EtOH/hexane