反应详情

To a solution of 2-(6-iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid benzylamide (100 mg, 0.23 mmol, 1.0 equiv) in dimethyl ether (1 mL) was added Na2CO3 (49 mg, 0.46 mmol, 2.0 equiv), trans-2-(4-fluorophenyl)vinyl boronic acid (95 mg, 0.57 mmol, 2.5 equiv), PdCl2(dppf) (17 mg, 0.02 mmol, 0.1 equiv) and water (0.1 mL) in a sealed tube. The reaction vessel was immersed in an oil bath preheated to 100° C. After stirring for 1 hr, the reaction mixture was cooled and the solvent was removed in vacuo. The crude product was purified by column chromatography [SiO2, methanol/dichloromethane, 0:100 to 5:95, v/v] and recrystallization (methanol/pentane) to give 2-{6-[(E)-2-(4-fluoro-phenyl)-vinyl]-pyrazin-2-yl}-4-methyl-thiazole-5-carboxylic acid benzylamide (59 mg, 60%). 1H NMR (400 MHz, CD2Cl2) δ 9.17 (s, 1H), 8.63 (s, 1H), 7.81 (d, J=16.0 Hz, 1H), 7.61-7.64 (m, 2H), 7.27-7.37 (m, 5H), 7.09-7.13 (m, 3H), 6.23 (bs, 1H), 4.61 (d, J=8.0 Hz, 2H), 2.74 (s, 3H); HRMS (M+H)+=431.13.

1. customThe reaction vessel was immersed in an oil bath
2. custompreheated to 100° C
3. temperaturethe reaction mixture was cooled
4. customthe solvent was removed in vacuo
5. customThe crude product was purified by column chromatography [SiO2, methanol/dichloromethane, 0:100 to 5:95, v/v] and recrystallization (methanol/pentane)