反应详情

温度

140 °C

A mixture of 3-hydroxy-N-(1-methyl-1H-pyrazol-3-yl)-5-[(3S)-tetrahydrofuran-3-yloxy]benzamide (539 mg, 1.77 mmol), N-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-3-chloro-2,4-difluoro-N-methylbenzamide (539 mg, 1.77 mmol) and potassium carbonate (490 mg, 3.55 mmol) in acetonitrile (15 mL) was placed in a Smith Creator microwave reactor and heated to 140° C. for 6 hours. Distilled water was added to the reaction and the aqueous layer extracted with DCM (3×30 mL). The combined organic phase was washed with brine (30 mL), dried (MgSO4), filtered and evaporated to give a yellow oil. This was purified by column chromatography, eluting with 20-100% ethyl acetate in isohexane, to give the title compound (290 mg). 1H NMR δ (CDCl3): 2.09-2.15 (1H, m), 2.18-2.27 (1H, m), 3.23 (3H, s), 3.59 (2H, t), 3.76 (3H, s), 3.86-3.92 (1H, m), 3.94-4.00 (3H, m), 4.54 (2H, t), 4.95 (1H, d), 6.68 (1H, d), 6.78-6.81 (2H, m), 7.04-7.05 (1H, m), 7.16-7.17 (1H, m), 7.28 (1H, d), 7.70 (1H, d), 8.75 (1H, s); m/z 513 (M+H)+.

1. extractionthe aqueous layer extracted with DCM (3×30 mL)
2. washThe combined organic phase was washed with brine (30 mL)
3. dry with materialdried (MgSO4)
4. filtrationfiltered
5. customevaporated
6. customto give a yellow oil
7. customThis was purified by column chromatography
8. washeluting with 20-100% ethyl acetate in isohexane