反应详情

To a solution of (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-[(4-bromo-4′-fluoro-5′-isopropyl-2′-methoxybiphenyl-2-yl)methyl]-4-methyl-1,3-oxazolidin-2-one (82.5 mg, 0.13 mmol) in 1,4-dioxane (1 mL) was added trimethylboroxin (39 mg, 0.31 mmol), Pd(PPh3)4 (15 mg, 10 mol %) and potassium carbonate (35 mg, 0.25 mmol). The resulting reaction mixture was purged with nitrogen and sealed in a microwave vessel. The vessel was subject to microwave irradiation at 130° C. for 15 min. The crude mixture was diluted with brine and extracted with EtOAc. The combined organic extracts were dried over Na2SO4. The titled compound was obtained as a glassy material after two preparative TLC plates developed respectively by 20% EtOAc in hexanes and dichloromethane. LC-MS: 584.08 (M+1)+. 1H NMR (CDCl3, 500 MHz) δ 1:1 mixture of rotamers δ 7.84 (s, 1 H), 7.65-7.70 (m, 2 H), 7.29 (s, 0.5), 7.18-7.22 (m, 1.5 H), 7.10-7.15 (m, 1 H), 7.01 (d, J=8.0 Hz, 0.5 H), 6.98 (d, J=8.5 Hz, 0.5 H), 6.66 (d, J=5.0 Hz, 0.5 H), 6.64 (d, J=5.5 Hz, 0.5 H), 5.54 (d, J=8.5 Hz, 0.5H), 5.31 (d, J=8.0 Hz, 0.5H), 4.82 (d, J=15.5 Hz, 1 H), 4.02 (d, J=15 Hz, 0.5 H), 3.71-3.82 (m, 5 H), 3.15-3.24 (m, 1 H), 2.42 (s, 1.5 H), 2.41 (s, 1.5 H), 1.13-1.27 (m, 6 H), 0.48 (d, J=6.5 Hz, 1.5 H), 0.31 (d, J=6.5 Hz, 1.5 H).

1. customThe resulting reaction mixture
2. customwas purged with nitrogen
3. customsealed in a microwave vessel
4. customirradiation at 130° C. for 15 min
5. additionThe crude mixture was diluted with brine
6. extractionextracted with EtOAc
7. dry with materialThe combined organic extracts were dried over Na2SO4