反应详情

温度

80 °C

A solution of 2-(morpholin-4-yl)-8-(trimethylstannyl)-5,6-dihydro-4H-[1,3]thiazolo[5,4-c]azepin-4-one (0.160 g, 0.386 mmol) and methyl-2-bromo-5-chlorobenzoate (0.116 g, 0.464 mmol) in DMF (3.74 mL) was purged with Argon, then added cesium fluoride (0.205 g, 1.35 mmol), copper(I) iodide (0.0184 g, 0.0966 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.0446 g, 0.0386 mmol). The mixture was stirred at 80° C. for 2 hours. The solution was cooled to room temperature, then evaporated some of the solvent. The residue was diluted with EA and water. The layers were separated and the aqueous layer was extracted twice more with EA. The combined organic layer was then washed with water and brine then dried over anhydrous sodium sulfate and concentrated. The residue was purified using column chromatography on silica gel (24 gr Analogix column, gradient DCM to 5% MeOH in DCM over 20 minutes) to give the product (0.129 g, 80%). LCMS: (AA) ES+ 420, 422. 1H NMR (300 MHz, d6-DMSO) δ: 7.95 (t, J=5.0 Hz, 1H), 7.71-7.67 (m, 1H), 7.66-7.59 (m, 1H), 7.39 (d, J=8.2 Hz, 1H), 6.28 (t, J=6.9 Hz, 1H), 3.66-3.57 (m, 6H), 3.47 (s, 3H), 3.30-3.25 (m, 4H).

1. temperatureThe solution was cooled to room temperature
2. customevaporated some of the solvent
3. additionThe residue was diluted with EA and water
4. customThe layers were separated
5. extractionthe aqueous layer was extracted twice more with EA
6. washThe combined organic layer was then washed with water and brine
7. dry with materialthen dried over anhydrous sodium sulfate
8. concentrationconcentrated
9. customThe residue was purified
10. customon silica gel (24 gr Analogix column, gradient DCM to 5% MeOH in DCM over 20 minutes)