Benzenepropanoic acid, 4-hydroxy-, methyl ester → 3-[4-(2-Isopropylsulfanyl-5-methyl-pyridin-3-ylmethoxy)-phenyl]-propionic acid

関与物質

反応手順

3-Chloromethyl-2-isopropylsulfanyl-5-methyl-pyridine (0.052 g, 0.24 mmol) obtained in Step D of Preparation Example 30 and 3-(4-hydroxy-phenyl)-propionic acid methyl ester (0.043 g, 0.24 mol) obtained in Preparation Example 4 were used to react sequentially in the same manner as in Steps A and B of Example 1 to obtain the title compound (55%).

情報源と証拠