Methanol → [8-Chloro-3-(4-chlorobenzyl)-4-methoxy-2-methylquinolin-5-yloxy]acetic acid

反応式

C[O:2][C:3](=[O:28])[CH2:4][O:5][C:6]1[CH:15]=[CH:14][C:13]([Cl:16])=[C:12]2[C:7]=1[C:8]([O:26][CH3:27])=[C:9]([CH2:18][C:19]1[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=1)[C:10]([CH3:17])=[N:11]2.CO.[OH-].[Li+]>O>[Cl:16][C:13]1[CH:14]=[CH:15][C:6]([O:5][CH2:4][C:3]([OH:28])=[O:2])=[C:7]2[C:12]=1[N:11]=[C:10]([CH3:17])[C:9]([CH2:18][C:19]1[CH:20]=[CH:21][C:22]([Cl:25])=[CH:23][CH:24]=1)=[C:8]2[O:26][CH3:27]

参加物

実験手順

A mixture of [8-chloro-3-(4-chlorobenzyl)-4-methoxy-2-methylquinolin-5-yloxy]acetic acid methyl ester (0.059 g), methanol (2.0 mL), saturated aqueous lithium hydroxide solution (0.25 mL) and water (0.4 mL) was stirred at room temperature for 15 hours, The methanol was removed under reduced pressure and the pH of the residue adjusted to 1 by the addition of 1.0 M aqueous hydrochloric acid. Purification by preparative reverse-phase HPLC using a gradient over 30 minutes of acetonitrile in water (20% to 80% of organic modifier) gave title compound as a yellow solid, 0.060 g.