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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70752생성일: 2026년 10월 23일

N-(9-Fluorenylmethoxycarbonyloxy)succinimide → Fmoc-Pro(4-OH)-OMe

https://huagongshe.com/ko/reaction/70752

반응식

참여 물질

역할이름HCID투입량
반응물N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
반응물4-Hydroxy-L-proline methyl ester hydrochlorideHCID 11435319—
용매sodium carbonate THFHCID 70538864—
생성물Fmoc-Pro(4-OH)-OMeHCID 68974574—

반응 단계

L-hydroxyproline methylester hydrochloride is reacted with Fmoc-OSu in aqueous 1.0 N sodium carbonate/THF at room temperature. After completion of the reaction, Fmoc-Pro(4-OH)—OMe is isolated by precipitation. Fmoc-Pro(4-OH)—OMe is then added dropwise into a solution of trisphosgene (0.6 eq.) in THF to give a chlorocarbonate intermediate. After 1 h dimethylaminopyridine (1.0 eq.) and N-Boc-diaminoethane (6.0 eq.) are added and the reaction is stirred at room temperature. After completion of the reaction, the solvent is removed in vacuo and the resulting Fmoc-Pro(4-OCO—NH—CH2—CH2—NH-Boc)-OMe is extracted from a two phase system of ethyl acetate/0.1 M HCl to give crude product (MH+=554) which is purified by crystallization from ethyl acetate. The methyl ester is then cleaved to the free acid by treatment with 1N NaOH in dioxane/water and the product Fmoc-Pro(4-OCO—NH—CH2—CH2—NH-Boc)-OH is purified on silica gel, [(M+Na)]+=562).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822637B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d2279bb155c64892bee7d04a8788917a
출처 메모uspto-grants-2014_09