反应详情

The title compound was synthesized in a similar manner as described for Example 1.1 using 8-bromo-1-(1-isopropyl-3-methyl-1H-pyrazol-4-yl)-3-methyl-1,3-dihydro-imidazo[4,5-c]quinolin-2-one (Intermediate G, 50 mg, 0.125 mmol) and 2-(dimethylamino)pyridine-5-boronic acid hydrate (Fluorochem Ltd., Derbyshire, United Kingdom, 31 mg, 0.163 mmol) to give the title compound as a yellow solid. (HPLC: tR 2.31 min (Method A); M+H=442 MS-ES; 1H-NMR (d6-DMSO, 400 MHz) 8.90 (s, 1H), 8.27-8.18 (m, 2H), 8.07-7.99 (m, 1H), 7.90-7.82 (m, 1H), 7.62-7.55 (m, 1H), 7.41 (s, 1H), 6.70-6.61 (m, 1H), 4.62-4.49 (m, 1H), 3.56 (s, 3H), 3.04 (s, 6H), 1.96 (s, 3H), 1.49 (s, 6H))

1. customThe title compound was synthesized in a similar manner