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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 546485생성일: 2026년 10월 26일

Ethyl 1-aminocyclopropane-1-carboxylate hydrochloride → (1R*,2S*)-N,N-Bis(tert-butoxycarbonyl)-4-[(1-ethoxycarbonyl)cyclopropan-1-yl]amino-1,2-cyclohexanediamine

https://huagongshe.com/reaction/546485

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 1-aminocyclopropane-1-carboxylate hydrochlorideHCID 386203—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(1R*,2S*)-N,N-bis(tert-butoxycarbonyl)-4-oxo-1,2-cyclohexanediamineHCID 68905437—
용매DichloromethaneHCID 6344—
생성물(1R*,2S*)-N,N-Bis(tert-butoxycarbonyl)-4-[(1-ethoxycarbonyl)cyclopropan-1-yl]amino-1,2-cyclohexanediamineHCID 68910855—

반응 단계

Ethyl 1-aminocyclopropanecarboxylate hydrochloride (1.63 g) was dissolved in dichloromethane (60 ml), and (1R*,2S*)-N,N-bis(tert-butoxycarbonyl)-4-oxo-1,2-cyclohexanediamine (3.0 g) and sodium triacetoxy-borohydride (2.51 g) were added to stir the mixture at room temperature for 3 hours. An aqueous solution of sodium hydrogencarbonate was added to separate an organic layer. The organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=3:1→1:1) to obtain the title compounds (Stereoisomer A: 1.43 g and Stereoisomer B: 2.17 g) as colorless amorphous solids.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07935824B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-c8777d626f9b4526bff323eb4b050885
출처 메모uspto-grants-2011_05