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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327526생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/327526

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 번호US05273982
출처 데이터셋uspto-grants-1993_12
ORD IDord-a8aadd92f54c4cd1a120c3378232101b
출처 메모uspto-grants-1993_12