Dimethylformamide → 6-tert-Butyl-2-(2-methyl-3-(5-(5-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-ylamino)-6-oxo-1,6-dihydropyridazin-3-yl)phenyl)isoindolin-1-one

関与物質

反応手順

A 250-mL single-neck round-bottomed flask equipped with a magnetic stirrer and nitrogen inlet was charged with 107e (890 mg, 2.20 mmol), 101m (441 mg, 1.57 mmol), sodium carbonate (832 mg, 7.85 mmol), DMF (5 mL), water (5 mL) and 1,4-dioxane (15 mL). After bubbling nitrogen through the resulting suspension for 30 min, tetrakis(triphenylphosphine)palladium(0) (363 mg, 0.314 mmol) was added. A reflux condenser was attached to the flask, and the reaction mixture was heated at reflux for 16 h. After this time, the mixture was diluted with ethyl acetate (100 mL) and water (50 mL), and the layers were separated. The aqueous layer was extracted with ethyl acetate (2×100 mL), and the combined organic layers were washed with brine (100 mL) and dried over sodium sulfate. The drying agent was removed by filtration. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by flash column chromatography (silica, 95:5 methylene chloride/methanol) to afford 107 in 27% yield (222 mg) as an amorphous white solid: mp 208-210° C.; 1H NMR (500 MHz, DMSO-d6) δ 12.97 (s, 1H), 9.21 (s, 1H), 7.79 (s, 1H), 7.75 (s, 1H), 7.75-7.73 (m, 1H), 7.60 (d, J=9.0 Hz, 1H), 7.48 (dd, J=7.5, 2.0 Hz, 1H), 7.40-7.38 (m, 2H), 5.96 (s, 1H), 4.84 (s, 2H), 3.97 (t, J=5.5 Hz, 2H), 3.51 (s, 2H), 2.79 (t, J=6.0 Hz, 2H), 2.35 (s, 3H), 2.10 (s, 3H), 1.36 (s, 9H); MS (ESI+) m/z 524.3 (M+H).

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