反应详情

温度

110 °C

7-bromo-3-chloro-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (1.05 g, 3.30 mmol), Pd2(dba)3 (8 mg, 0.00825 mmol), BINAP (15 mg, 0.0248 mmol) and benzophenone imine (0.662 mL, 3.95 mmol) were combined in a dry flask. The flask was charged with 40 mL of dry toluene, followed by sodium tert-butoxide (0.444 g, 4.62 mmol). Argon was bubbled through the solution for 5 minutes. The reaction solution was heated to 110° C. and stirred under argon. After 2.5 hours, the reaction was concentrated, 20 mL of THF and 1 mL of 6N hydrochloric acid were added and the resulting solution was stirred. After 2 hours, the solution was poured into 300 mL of ethyl acetate, 100 mL of saturated sodium bicarbonate and 200 mL of water. The organic layers were separated, dried with magnesium sulfate, filtered, concentrated, and purified by flash column chromatography (0-30% ethyl acetate/hexanes gradient) to afford the title compound. 1H NMR (600 MHz, CDCl3) δ 8.77 (d, 1H); 8.55 (d, 1H); 7.58 (d, 1H); 7.44 (d, 1H); 7.18 (d, 1H); 7.14 (d, 1H); 7.01 (dd, 1H); 4.15 (s, 2H). LRMS (APCI) calculated for C14H10ClN2O [M+H]+, 257.0; found 257.1.

1. customArgon was bubbled through the solution for 5 minutes
2. concentrationthe reaction was concentrated
3. addition20 mL of THF and 1 mL of 6N hydrochloric acid were added
4. stirringthe resulting solution was stirred
5. waitAfter 2 hours
6. additionthe solution was poured into 300 mL of ethyl acetate, 100 mL of saturated sodium bicarbonate and 200 mL of water
7. customThe organic layers were separated
8. dry with materialdried with magnesium sulfate
9. filtrationfiltered
10. concentrationconcentrated
11. custompurified by flash column chromatography (0-30% ethyl acetate/hexanes gradient)