Tetrahydrofuran → (5-(5-(3-Chloro-4-isobutylphenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methanol

関与物質

反応手順

The crude product of the title compound was synthesized by conducting the similar reaction to that mentioned in Example 12 (12a) using 3-chloro-4-isobutylbenzoic acid (0.13 g, 0.61 mmol) that was obtained in Example 24 (24h), 1-hydroxybenzotriazole (86 mg, 0.64 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.12 g, 0.64 mmol), 6-({[t-butyl(dimethyl)silyl]oxy}methyl)-N′-hydroxypyridine-3-carboximidamide (0.16 g, 0.58 mmol) that was obtained in Example 23 (23c), and a 1.0 M solution of tetrabutylammonium fluoride in tetrahydrofuran (1.2 ml, 1.2 mmol). Subsequently, the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (2:3 to 1:1) as the eluent to afford the title compound (0.19 g) in a yield of 94% as a white crystalline solid.

情報源と証拠