反应详情

温度

100 °C

To a degassed solution of 2-(2-methoxypyridin-4-yl)-N-methyl-6-(N-methylmethylsulfonamido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzofuran-3-carboxamide (60 mg, 0.12 mmol), 2-chloro-11-fluoro-6H-pyrido[2′,3′:5,6][1,3]oxazino[3,4-a]indole (35 mg, 0.13 mmol) and Na2CO3 (25 mg, 0.23 mmol) in dioxane (1.5 mL) and H2O (0.1 mL) was added Pd2(dba)3 (3 mg) and X-Phos (3 mg) under N2. Then the mixture was stirred at 100° C. for 2 hours. The reaction mixture was cooled to RT and filtered. The filtrate was washed with H2O and dried over Na2SO4. After concentrated, the residue was purified by prep-HPLC to give the product of 5-(11-fluoro-6H-pyrido[2′,3′:5,6][1,3]oxazino[3,4-a]indol-2-yl)-2-(2-methoxypyridin-4-yl)-N-methyl-6-(N-methylmethylsulfonamido)benzofuran-3-carboxamide (35 mg, yield: 48%). 1H-NMR (CDCl3, 400 MHz) δ 8.29 (s, 1H), 8.28 (s, 1H), 7.98 (s, 1H), 7.69 (s, 2H), 7.40˜7.49 (m, 1H), 7.30 (s, 1H), 7.19˜7.24 (m, 2H), 7.10˜7.18 (m, 1H), 6.82˜6.87 (m, 1H), 6.11 (s, 1H), 5.99 (s, 2H), 3.99 (s, 3H), 3.36 (s, 3H), 3.04 (d, J=4.8 Hz, 3H), 2.75 (s, 3H). MS (M+H)+: 628.

1. temperatureThe reaction mixture was cooled to RT
2. filtrationfiltered
3. washThe filtrate was washed with H2O
4. dry with materialdried over Na2SO4
5. concentrationAfter concentrated
6. customthe residue was purified by prep-HPLC