反应详情

The title compound was prepared as described in Example 18 starting with 6-bromo-5,6-dihydro-7-hydroxy-5,5-dimethyl-7H-thieno[3,2-b]pyran (1.5 g, 5.7 mmol) and piperidine (1.7 mL, 17.1 mmol) in N,N-dimethylformamide (25 mL) to give an off white solid, 0.977 (64%): mp 68°-70° C.; IR (KBr): 2937, 1549 and 1396 cm-1 ; MS: m/z 162 (MH+); 1H NMR (CDCl3): δ1.20(s, 3H), 1.50(s, 3H), 1.52(m, 2H), 1.61(m, 4H), 2.65(m, 2H), 2.78(m, 2H), 3.20(bs, 1H, exchanges with D2O), 3.55(d, J=9.3 Hz, 1H), 3.68(d, J=9.3 Hz, 1H), 6.58(d, J=5.4 Hz, 1H) and 7.04(d, J=5.4 Hz, 1H).