反应详情

The title compound was prepared from 2,6-diisopropyl-3-hydroxymethyl-4-(4-fluorophenyl)-5butylpyridine (Example 24) according to the procedures described in Example 101. 1H NMR (300 MHz, CDCl3): δ 7.1 (m, 4 H), 4.7 (dq, J=3 Hz, 1 H), 3.7 (septet, J=7 Hz, 1 H), 3.2 (septet, J=7 Hz, 1 H), 2.2 (t, J=1.5 Hz, 2 H), 1.6 (d, J=5 Hz, 1 H), 1.4 (d, J=7 Hz, 3 H), 1.3 (m, 16 H), 0.8 (t, J=7Hz, 3H). FAB-MS: calcd for (C23H32FNO) 357, found 358 (M+H). mp 103-104° C. Rf=0.2 (60% CH2Cl2/hexane).