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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1647122생성일: 2026년 10월 27일

Tert-butyl (2S)-2-amino-3-[4-(tert-butoxy)phenyl]propanoate → Piperidine

https://huagongshe.com/reaction/1647122

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl (2S)-2-amino-3-[4-(tert-butoxy)phenyl]propanoateHCID 7350495—
반응물N-[(9H-fluoren-9-yloxy)carbonyl]-3-(t-butoxycarbonyl)-L-alanineHCID 54139735—
생성물PiperidineHCID 8082—
생성물N-[N-[(9H-fluoren-9-yloxy)carbonyl]-3-(t-butoxycarbonyl)-L-alanyl]-3-(p-t-butoxyphenyl)-L-alanine t-butyl esterHCID 22849520—

반응 단계

N-[(9H-fluoren-9-yloxy)carbonyl]-3-(t-butoxycarbonyl)-L-alanine and 3-(p-t-butoxyphenyl)-L-alanine t-butyl ester were coupled to give N-[N-[(9H-fluoren-9-yloxy)carbonyl] -3-(t-butoxycarbonyl)-L-alanyl]-3-(p-t-butoxyphenyl)-L-alanine t-butyl ester and 5 ml of piperidine and the reaction solution was evaporated. The residue was suspended in methanol and insoluble material was filtered off. The filtrate was evaporated and chromatographed on silica gel using ethyl acetate to yield 2 g of 3-(t-butoxyphenyl)-N-[3-(p-t-butoxy-carbonyl)-L-alanyl]-L-alanine t-butyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05430024
출처 데이터셋uspto-grants-1995_07
ORD IDord-7f5bcbe068aa4c0da47b21ff0835966c
출처 메모uspto-grants-1995_07