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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20083생성일: 2026년 10월 23일

Acetic Acid → Benzyl 4-{[1-(methoxycarbonyl)but-3-en-1-yl]amino}piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/20083

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물Methyl 2-aminopent-4-enoateHCID 10877146—
용매1,1-DichloroethaneHCID 6365—
생성물Benzyl 4-{[1-(methoxycarbonyl)but-3-en-1-yl]amino}piperidine-1-carboxylateHCID 22293179103.4%

반응 단계

Sodium triacetoxyborohydride (11.2 g, 52.6 mmol) was added to a solution of methyl 2-aminopent-4-enoate (3.4 g, 26.3 mmol), acetic acid (2.37 g, 39.5 mmol) and benzyl 4-oxopiperidine-1-carboxylate (9.21 g, 39.5 mmol) in dichloroethane (60 mL) at room temperature. After 3 h, the reaction was quenched with saturated aqueous sodium bicarbonate, extracted with methylene chloride (3×), dried over sodium sulfate, filtered and evaporated to give the crude product. This was purified by chromatography (silica gel, 0 to 8% methanol in methylene chloride gradient elution), which gave the title compound (9.42 g). MS 347.2 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745427B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-33c0580e28f64c06ae5e7467e5c2b669
출처 메모uspto-grants-2010_06