反应详情

To a mixture of 3-(2-methoxy-phenyl)-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine (504 mg, 1 mmol) and 3-(3-bromo-phenyl)-3-(1,1-dioxothiomorpholin-4-yl)-propionic acid (362 mg, 1.0 mmol) in a 20 mL microwave reaction flask was added THF (3 mL), acetonitrile (3 mL) and sodium carbonate (3 mL, 1 N aqueous solution, 3 mmol). The mixture was purged with nitrogen for 1 minute. Dichloro[1,1′-bis(diphenylphoshino)ferrocene]palladium(II) dichloromethane adduct (82 mg, 0.1 mol) was added and the purging continued for another minute. The flask was sealed and irradiated in a microwave reactor to 135° C. for 20 minutes. Saturated sodium chloride (10 mL) was added and the pH was adjusted to 5 using hydrochloric acid (1 N). The resulting mixture was extracted with ethyl acetate (10 mL×3). The combined organic layers were dried over sodium sulfate, filtered, and concentrated. The residue was purified by flash chromatography on silica gel using a gradient of methanol in dichloromethane to afford 3-(1,1-dioxothiomorpholin-4-yl)-3-{3-[3-(2-methoxy-phenyl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-phenyl}-propionic acid as a yellow solid (353 mg, 53% yield). MS: m/z 660 (M+H+).

1. customin a 20 mL microwave reaction flask
2. customThe mixture was purged with nitrogen for 1 minute
3. customThe flask was sealed
4. customirradiated in a microwave reactor to 135° C. for 20 minutes
5. extractionThe resulting mixture was extracted with ethyl acetate (10 mL×3)
6. dry with materialThe combined organic layers were dried over sodium sulfate
7. filtrationfiltered
8. concentrationconcentrated
9. customThe residue was purified by flash chromatography on silica gel using a gradient of methanol in dichloromethane