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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60900생성일: 2026년 10월 25일

Carbamate → (2S,3R)-Allyl 2-(aminomethyl)-3-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/60900

반응식

참여 물질

역할이름HCID투입량
반응물CarbamateHCID 276—
반응물Allyl chloroformateHCID 18052—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물DiisopropylethylamineHCID 81531—
반응물2-(((2S,3R)-3-Methylpiperidin-2-yl)methyl)isoindoline-1,3-dioneHCID 117727630—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물(2S,3R)-Allyl 2-(aminomethyl)-3-methylpiperidine-1-carboxylateHCID 89748216—

반응 단계

To a solution of 2-(((2S,3R)-3-methylpiperidin-2-yl)methyl)isoindoline-1,3-dione (5 g, 19.4 mmol) in CH2Cl2 at 0° C. was added DIPEA (3.8 mL), followed by allyl chloroformate (2.6 mL). The reaction was allowed to warm to rt overnight. After 16 h, the reaction was concentrated to remove the CH2Cl2, and then re-suspended in EtOAc and washed with 1 M HCl (2×), brine (2×), dried (MgSO4) and concentrated to give the crude carbamate which was used without further purification. A mixture of the crude carbamate and hydrazine hydrate (2 g, 39 mmol) in MeOH (100 mL) was heated at 60° C. for 2 h. The mixture was cooled to rt and the solvent was removed in vacuo. The crude was dissolved in EtOAc and washed with 2 N NaOH (2×), brine, and then dried (Na2SO4). The solvent was removed in vacuo to obtain the title compound which was used without further purification. ESI-MS (m/z): 213 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440982B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-fbf016bb74e441ada4a45e7d402b144f
출처 메모uspto-grants-2016_09