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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1099512생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1099512

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium BicarbonateHCID 516892—
반응물IsocyanocyclopropaneHCID 2758008—
반응물(S)-2-(dibenzylamino)pentanalHCID 44223341—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물(2S,3S)-1-(cyclopropylamino)-3-(dibenzylamino)-1-oxohexan-2-yl acetateHCID 44594157—

반응 조건

온도27.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143448B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-17fb77a7952b41eab4f32262ae1b570a
출처 메모uspto-grants-2012_03