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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 534158생성일: 2026년 10월 25일

Acetic Acid → Tert-butyl 4-(2-(((trans)-2-phenylcyclopropyl)amino)ethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/534158

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물(1R,2S)-TranylcypromineHCID 19493—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물tert-Butyl 4-(2-oxoethyl)piperidine-1-carboxylateHCID 10353694—
용매ChloroformHCID 6212—
생성물Tert-butyl 4-(2-(((trans)-2-phenylcyclopropyl)amino)ethyl)piperidine-1-carboxylateHCID 68385104—

반응 단계

A mixture of [trans-2-phenylcyclopropyl]amine (668 mg, 5.02 mmol), 1,1-dimethylethyl 4-(2-oxoethyl)-1-piperidinecarboxylate (1.04 g, 4.58 mmol) and AcOH (1 μL, 0.017 mmol) in chloroform (5 mL) was stirred at room temperature for 18 hours. Sodium triacetoxyborohydride (1.03 g, 4.86 mmol) was added and stirring continued for 18 hours. Upon completion, saturated NaHCO3 was added to the reaction mixture and the mixture was extracted with THF—CHCl3 (2×50 mL). The organics were combined, dried over Na2SO4 and concentrated. The residue was adsorbed onto silica and purified via column chromatography on the ISCO Companion (gradient 0-100% 80:20:2 [CHCl3/MeOH/NH4OH]/CHCl3; 12 g column) to yield the desired product. This product was further purified via reverse phase column chromatography on Gilson ((C18 column: 0.1% Formic acid H2O/CH3CN, 95-5%) affording the title compound (222 mg, 13% yield) as a yellow oil: LC-MS (ES) m/z=345 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853408B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-27b640b3e8264b11b96f921a5fb267b8
출처 메모uspto-grants-2014_10