反应详情

To a solution of (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-(2-bromo-5-fluorobenzyl)-4-methyl-1,3-oxazolidin-2-one (1.0 g, 2.0 mmol) in 1,4-dioxane (6 mL) was added (4-fluoro-5-isopropyl-2-methoxyphenyl)boronic acid (509 mg, 2.4 mmol), [1,1′-bis(diphenylphosphino) ferrocene]dichloropalladium (II) (82 mg, 5 mol %) and aq. potassium hydroxide (1.3 mL, 3M, 2 eq.). The reaction mixture was purged with nitrogen and then sealed in a microwave vessel. The reaction vessel was subject to microwave irradiation at 150° C. for 40 min. Crude mixture was worked up with water. Volatiles were evaporated. The resulting mixture was extracted with EtOAc. The combined extracts were dried over Na2SO4. The resulting purple residue was purified by SiO2 (Biotage 40+M cartridge, eluted by EtOAc/hexane, gradient; 5% to 25%). The titled compound was obtained as clear solid. LC-MS: 588.23 (M+1)+. 1H NMR (CDCl3, 500 MHz) δ 6:4 mixture of rotamers δ 7.85 (s, 1 H), 7.69 (s, 2 H), 7.16-7.21 (m, 1.5 H), 7.04-7.13 (m, 1.5 H), 6.96 (dd, J=14.3, 8.80 Hz, 1 H), 6.65 (d, J=10.0 Hz, 1H), 5.59 (d, J=8.0 Hz, 0.6H), 5.43 (d, J=8.0 Hz, 0.4H), 4.85 (d, J=15.8 Hz, 0.6H), 4.82 (d, J=15.8 Hz, 0.4H), 4.02 (d, J=15.8 Hz, 0.6 H), 3.85 (m, 0.6 H), 3.76-3.81 (m, 0.8 H), 3.75 (s, 1.8H), 3.73 (s, 1.2H), 3.19 (m, 1H), 1.14-1.26 (m, 6 H), 0.56 (d, J=6.6 Hz, 1.2 H), 0.38 (d, J=6.6 Hz, 1.8 H).

1. customThe reaction mixture was purged with nitrogen
2. customsealed in a microwave vessel
3. customirradiation at 150° C. for 40 min
4. customVolatiles were evaporated
5. extractionThe resulting mixture was extracted with EtOAc
6. dry with materialThe combined extracts were dried over Na2SO4
7. customThe resulting purple residue was purified by SiO2 (Biotage 40+M cartridge, eluted by EtOAc/hexane, gradient; 5% to 25%)