反应详情

Prepared in a similar manner to Example 1 from 2-(4-bromophenyl)-N-isobutyl-2-methylpropanamide (example 1a) and 3-(methoxymethyl)phenylboronic acid. Yield: 91%. 1H NMR (400 MHz, DMSO): δ 0.72-0.74 (d, 6H), 1.46 (s, 6H), 1.68 (m, 1H), 2.83 (t, 2H), 3.29 (s, 3H), 4.45 (s, 2H), 7.27-7.29 (d, 1H), 7.33 (t, 1H), 7.36-7.38 (d, 2H), 7.41 (t, 1H), 7.53-7.55 (d, 2H), 7.58-7.60 (d, 2H). MS (M+H, 340).