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HRID 1365709作成日:2026年10月26日

Water → (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(methyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid

https://huagongshe.com/reaction/1365709

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Lithium HydroxideHCID 3939—
反応物(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(methyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl esterHCID 57762554—
溶媒TetrahydrofuranHCID 8028—
生成物(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(methyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acidHCID 1151883981.3%

反応条件

温度0 °C

反応手順

A solution of (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(methyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl ester (1.28 g) in THF (45 ml) was cooled to 0° C. To the solution, 0.1N aqueous lithium hydroxide solution (40 ml) was added, and the resulting mixture was stirred at 0° C. for 40 minutes. Water (50 ml) was added to the reaction solution, and the resulting mixture was washed with ether. Aqueous layer was acidified by adding 1N hydrochloric acid in small portions thereto, and extracted twice 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 to dryness to obtain (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(methyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid (1.01 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893046B2
出典データセットuspto-grants-2011_02
ORD IDord-a54528950ffb4d0d9cf977e9fc0f848f
出典メモuspto-grants-2011_02