反应详情

Using the conditions of General Procedure B for Suzuki Coupling and Hydrolysis in Parallel Mode, 2-bromo-5-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-benzoic acid methyl ester (which may be prepared as described for Intermediate 6; 89 mg, 0.2 mmol) was reacted with and 2-chloro-5-methoxyphenylboronic acid (available from Combi-Blocks Inc.; 75 mg, 0.4 mmol). The resulting ester was hydrolyzed and the acid was purified to give 2′-chloro-4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-5′-methoxy-biphenyl-2-carboxylic acid (29 mg, 29%). 1H NMR (400 MHz, DMSO-d6) δ 13.04 (br s, 1H), 8.45-8.58 (m, 2H), 8.34 (d, J=2.0 Hz, 1H), 8.26 (dd, J=7.9, 1.9 Hz, 1H), 8.09 (dd, J=8.4, 1.9 Hz, 1H), 7.77 (d, J=8.5 Hz, 1H), 7.46 (d, J=8.0 Hz, 1H), 7.40 (d, J=8.8 Hz, 1H), 6.98 (dd, J=8.8, 3.0 Hz, 1H), 6.92 (d, J=3.0 Hz, 1H), 3.79 (m, 3H).

1. customthe acid was purified