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HRID 230375作成日:2026年10月25日

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

https://huagongshe.com/reaction/230375

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-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl esterHCID 57762568—
溶媒TetrahydrofuranHCID 8028—
生成物(S,E)-2-(2,6-dichlorobenzamido)-5-[4-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acidHCID 116850490.1%

反応条件

温度0 °C

反応手順

A solution of (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl ester (526.2 g) in THF (15 ml) was cooled to 0° C. To the solution, 0.1N aqueous lithium hydroxide solution (15.4 ml) was added, and the resulting mixture was stirred at 0° C. for 40 minutes. Water (20 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-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid (420.7 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566724B2
出典データセットuspto-grants-2009_07
ORD IDord-11c301b2141643b080adbaad33b2c362
出典メモuspto-grants-2009_07