反应详情

The title compound was prepared as described in Example 3 starting with 6-bromo-7-hydroxy-5,6-dihydro-5,5-dimethyl-7H-thieno[3,2-b]pyran (4.5 g, 17.1 mmol) and 4-trifluoromethylbenzamide (7.43 g, 39.3 mmol) in N,N-dimethylformamide (75 mL) to give the product, 1.96 g (31%), as a colorless solid: mp 162°-163° C.; IR (KBr): 3396, 1664, 1534 and 1507 cm-1 ; MS: m/z 372 (MH+); 1H NMR (DMSO-d6): δ 1.21 (s, 3H), 1.40 {s, 3H), 3.80 (m, 1H, simplifies to d, J=8.7 Hz, with D2O), 5.01 (m, 1H, simplifies to d, J=8.7 Hz, with D2O), 5.68 (d, J=6.0 Hz, 1H, exchanges with D2O), 6.59 (d, J=5.7 Hz, 1H), 7.31 (d, J= 5.7 Hz, 1H), 7.88 (d, J=8.3 Hz, 2H), 8.11 (d, J=8.3 Hz, 2H) and 9.05 (d, J=8.4 Hz, 1H exchanges with D2O).

1. customto give the product, 1.96 g (31%)