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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2061043생성일: 2026년 10월 27일

Methyl iodide → 1-(2-(3-(Benzyloxycarbonylamino)-3-methylbutanoyloxy)ethyl)-1-methylpiperidinium iodide

https://huagongshe.com/reaction/2061043

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물2-(Piperidin-1-yl)ethyl 3-(benzyloxycarbonylamino)-3-methylbutanoateHCID 60134458—
용매DichloromethaneHCID 6344—
생성물1-(2-(3-(Benzyloxycarbonylamino)-3-methylbutanoyloxy)ethyl)-1-methylpiperidinium iodideHCID 6731061666.4%

반응 단계

A batch of 2-(piperidin-1-yl)ethyl 3-(benzyloxycarbonylamino)-3-methylbutanoate (9.45 g, 26.1 mmol) was dissolved in a solution of dichloromethane (40 ml) and methyl iodide (16.3 ml, 262 mmole). The mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated in vacuo, and the crude material was purified by pre-HPLC to give 8.74 g (66%) of 1-(2-(3-(benzyloxycarbonylamino)-3-methylbutanoyloxy)ethyl)-1-methylpiperidinium iodide. 1H NMR (CD3OD) δ 7.39-7.27 (m, 5 H), 5.05 (s, 2 H), 4.52-4.47 (m, 2 H), 3.70-3.64 (m, 2 H), 3.44-3.37 (m, 4 H), 3.09 (s, 3 H), 2.84 (s, 2 H), 1.92-1.86 (m, 4 H), 1.73-1.59 (m, 2 H), 1.39 (s, 6 H). MS (ESI+) calculated for C21H33N2O4+: 377.24, Found: 377.2 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08278482B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-ee26e2c2ed8b41c7b912640d4d442c61
출처 메모uspto-grants-2012_10