反应详情

温度

92.5 °C

A mixture of 7-(1-(2,6-Dichloro-3-fluorophenyl)ethoxy)-3-bromo-6-nitrofuro[3,2-c]pyridine (12.6 g, 28.1 mmol), tert-butyl 5,6-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-1(2H)-carboxylate (9.56 g, 30.9 mmol) and dioxane/water (4:1, 120 mL/30 mL) in a 500-mL round-bottom flask was stirred and degassed with nitrogen for 15 min. To the solution, Pd(PPh3)2Cl2 (400 mg, 0.57 mmol) was added followed by potassium carbonate (5.82 g, 42.19 mmol) was added and degassed with nitrogen for another 5 min. The mixture was heated at 90-95° C. for 2.5 h. TLC (5% methanol in dichloromethane) indicated completion of the reaction. The mixture was cooled to RT, and solvent was removed on rotary evaporator. To the residue, water (60 mL) and dichloromethane (150 mL) were added. The organic layer was separated and the aqueous layer was extracted with dichloromethane (2×60 mL). All organic layers were combined and washed with brine solution (60 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with 1:1 ethyl acetate and dichloromethane to give the title compound. 1H NMR (CDCl3, 300 MHz): δ=1.45 (s, 9H), 1.95 (d, J=6.6 Hz, 3H), 2.45 (brs, 2H), 3.62 (t, J=6.0 Hz, 2H), 4.18 (t, J=3.0 Hz, 2H), 6.25 (brs, 1H), 6.63 (t, J=6.0 Hz, 1H), 7.05 (m, 1H), 7.21 (m, 1H), 7.69 (s, 1H), 8.60 (s, 1H).

1. customdegassed with nitrogen for 15 min
2. additionwas added
3. customdegassed with nitrogen for another 5 min
4. customcompletion of the reaction
5. temperatureThe mixture was cooled to RT
6. customsolvent was removed on rotary evaporator
7. additionTo the residue, water (60 mL) and dichloromethane (150 mL) were added
8. customThe organic layer was separated
9. extractionthe aqueous layer was extracted with dichloromethane (2×60 mL)
10. washwashed with brine solution (60 mL)
11. dry with materialdried over anhydrous sodium sulfate
12. filtrationfiltered
13. concentrationconcentrated under reduced pressure
14. customThe residue was purified by column chromatography on silica gel eluting with 1:1 ethyl acetate and dichloromethane