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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339014생성일: 2026년 10월 24일

Pyridine → (S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoate

https://huagongshe.com/ko/reaction/339014

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Benzyl chloroformateHCID 10387—
반응물N-Boc-L-serine methyl esterHCID 7019177—
용매DichloromethaneHCID 6344—
생성물(S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoateHCID 7098417589.4%

반응 단계

A solution of N-(tert-butoxycarbonyl)-L-serine methyl ester (25.0 g, 114 mmol) in DCM (570 mL) was cooled to −50° C. Pyridine (23.0 mL, 285 mmol) was added. CBZ-Cl (18.9 mL, 125 mmol) was added dropwise over 1 hour. The reaction mixture was warmed to ambient temperature and stirred overnight. The reaction mixture was then diluted with DCM, washed with 10% citric acid and brine, dried and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (5:1 hexanes/EtOAc) to give (S)-methyl 3-(benzyloxycarbonyloxy)-2-(tert-butoxycarbonylamino)propanoate (36.0 g, 89%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889704B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-93ab199918194d77951dc27dd95c2847
출처 메모uspto-grants-2014_11