反应详情

A solution of 2-methoxy-4-(methylthio)benzoic acid (5.0 g, 25.2 mmol) in dichloromethane (50 mL) was cooled to 0° C. and treated with oxalyl chloride (6.6 mL, 75.6 mmol). A drop of N,N-dimethylformamide was added and the reaction was heated to a gentle reflux for 2 h. After cooling to room temperature, the solution was concentrated in vacuo to remove the excess oxalyl chloride, diluted with dichloromethane (53 mL) and cooled to 0° C. The resulting solution was treated with N,N-diisopropylethylamine (11.6 mL, 67 mmol) and 4-bromo-2-fluorobenzylamine hydrochloride (9.7 g, 40.2 mmol). The resulting solution was stirred at room temperature overnight, concentrated in vacuo, diluted with ethyl acetate and successively washed with 2 N HCl and saturated NaCl. The organic layer was dried over MgSO4, filtered and concentrated. Rf 0.4 (40% ethyl acetate in heptane); 1H NMR (DMSO-d6 300 MHz) δ 8.63 (t, J=6 Hz, 1H), 7.70 (d, J=8.1 Hz, 1H), 7.50 (dd, J1=9.6 Hz, J2=2.1 Hz, 1H), 7.38 (dd, J1=8.4 Hz, J2=2.0 Hz , 1H), 7.28 (t, J=8.4 Hz, 1H), 6.94 (br s , 1H), 6.89 (dd, J1=5.7 Hz, J2=1.7 Hz, 1H), 4.46 (d, J=6 Hz, 2 H), 3.91 (s, 3H), 2.51 (s, 3H).

1. temperaturethe reaction was heated to
2. temperaturea gentle reflux for 2 h
3. concentrationthe solution was concentrated in vacuo
4. customto remove the excess oxalyl chloride
5. additiondiluted with dichloromethane (53 mL)
6. temperaturecooled to 0° C
7. concentrationconcentrated in vacuo
8. additiondiluted with ethyl acetate
9. washsuccessively washed with 2 N HCl and saturated NaCl
10. dry with materialThe organic layer was dried over MgSO4
11. filtrationfiltered
12. concentrationconcentrated