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HRID 1752094作成日:2026年10月25日

Barium hydroxide, octahydrate → (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid

https://huagongshe.com/reaction/1752094

反応式

関与物質

役割名称HCID仕込み量
反応物Barium hydroxide, octahydrateHCID 17749109—
反応物(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl esterHCID 57762529—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acidHCID 1153340664.6%

反応条件

温度0 °C

反応手順

In a mixed solvent of THF (250 ml) and water (125 ml), (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl ester (9.80 g) was dissolved, and the resulting mixture was cooled to 0° C. Barium hydroxide octahydrate (3.14 g) was added thereto and the resulting mixture was stirred at 0° C. for 8 hours. The reaction solution was concentrated to remove THF, and water (150 ml) was added thereto, followed by washing the resulting mixture with ether. Aqueous layer was acidified by adding 1N hydrochloric acid in small portions thereto and extracted 3 times with ethyl acetate. Organic layers were washed with saturated brine and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: chloroform/methanol=10/1). The obtained crude product was further purified by column chromatography (silica gel, eluent: cyclohexane/ethyl acetate=1/1→ethyl acetate) to obtain (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(4-methoxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid (6.15 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09162988B2
出典データセットuspto-grants-2015_10
ORD IDord-7d015e262b4541d1a628450748d8f32a
出典メモuspto-grants-2015_10