Aluminium lithium hydride → 3-(4-((3-(4-Ethylphenyl)-5-methylthiophen-2-yl)methoxy)-2,3-difluorophenyl)propan-1-ol
反応式
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH2:7]([C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:19]=[C:18]([CH3:20])[S:17][C:16]=2[CH2:21][O:22][C:23]2[CH:28]=[CH:27][C:26]([CH2:29][CH2:30][C:31](OCC)=[O:32])=[C:25]([F:36])[C:24]=2[F:37])=[CH:11][CH:10]=1)[CH3:8]>>[CH2:7]([C:9]1[CH:10]=[CH:11][C:12]([C:15]2[CH:19]=[C:18]([CH3:20])[S:17][C:16]=2[CH2:21][O:22][C:23]2[CH:28]=[CH:27][C:26]([CH2:29][CH2:30][CH2:31][OH:32])=[C:25]([F:36])[C:24]=2[F:37])=[CH:13][CH:14]=1)[CH3:8]参加物
3
実験手順
The title compound was prepared according to the procedure described in Example 223 by LAH reduction of ethyl 3-(4-((3-(4-ethylphenyl)-5-methylthiophen-2-yl)methoxy)-2,3-difluoro phenyl)propanoate to give the desired product as off-white oil. 1H NMR (400 MHz, CDCl3) δ 7.35 (d, J=7.0 Hz, 2H), 7.24 (d, J=7.1 Hz, 2H), 6.78 (s, 1H), 6.72 (m, J=5.8 Hz, 1H), 6.62 (m, J=7.2 Hz, 1H), 5.11 (s, 2H), 3.72 (t, J=8.1 Hz, 2H), 2.72 (m, J=5.2 Hz, 2H), 2.65 (m, J=7.5 Hz, 2H), 2.49 (s, 3H), 1.82 (m, J=5.8 Hz, 2H), 1.70 (br, s, 1H), 1.28 (t, J=7.2 Hz, 3H).