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HRID 1099512作成日:2026年10月27日

Acetic Acid → (2S,3S)-1-(cyclopropylamino)-3-(dibenzylamino)-1-oxohexan-2-yl acetate

https://huagongshe.com/reaction/1099512

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium BicarbonateHCID 516892—
反応物IsocyanocyclopropaneHCID 2758008—
反応物(S)-2-(dibenzylamino)pentanalHCID 44223341—
溶媒DichloromethaneHCID 6344—
溶媒HexaneHCID 8058—
生成物(2S,3S)-1-(cyclopropylamino)-3-(dibenzylamino)-1-oxohexan-2-yl acetateHCID 44594157—

反応条件

温度27.5 °C

反応手順

To a cooled (0-5° C.) solution of (S)-2-(dibenzylamino)pentanal in dichloromethane (210 mL) was added cyclopropylisonitrile followed by acetic acid at 0-5° C. The reaction mixture temperature was raised to 25-30° C. over 40-60 minutes, and stirred for 16-18 hours at 25-30° C. Progress of the reaction was monitored by TLC analysis. When the reaction was complete, the mixture was cooled to 0-5° C., and saturated sodium bicarbonate solution (200 mL) was added. The organic layer was separated and the aqueous layer was extracted with dichloromethane twice. The combined organic layers were washed with water (1×200 mL), brine (1×200 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The crude product thus obtained was slurried in hexane (150 mL) and stirred for one hour at 25-35° C. The slurry was filtered and the solid washed with hexane and dried under reduced pressure to provide 17.0 g of (2S,3S)-1-(cyclopropylamino)-3-(dibenzylamino)-1-oxohexan-2-yl acetate as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143448B2
出典データセットuspto-grants-2012_03
ORD IDord-17fb77a7952b41eab4f32262ae1b570a
出典メモuspto-grants-2012_03