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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2361986생성일: 2026년 10월 24일

Fmoc-L-Tyr(tBu)-OH → (9H-fluoren-9-yl)methyl (S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-1-oxopropan-2-ylcarbamate

https://huagongshe.com/ko/reaction/2361986

반응식

참여 물질

역할이름HCID투입량
반응물Fmoc-L-Tyr(tBu)-OHHCID 10895791—
반응물(S)-1,1-diethoxy-N-(naphthalen-1-ylmethyl)propan-2-amineHCID 67075196—
생성물(9H-fluoren-9-yl)methyl (S)-3-(4-tert-butoxyphenyl)-1-(((S)-1,1-diethoxypropan-2-yl)(naphthalen-1-ylmethyl)amino)-1-oxopropan-2-ylcarbamateHCID 8669852679.1%

반응 단계

According to the procedure described in the synthesis method of Compound III-5, (S)-1,1-diethoxy-N-(naphthalen-1-ylmethyl)propan-2-amine (Compound IX-6) (686 mg, 2.4 mmol) was coupled with (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-tert-butoxyphenyl)propanoic acid (1.15 g, 2.51 mmol) and the obtained residue was purified by Büch silica gel column chromatography (eluent: n-hexane:ethyl acetate=7:3) to obtain the title compound (1.384 g, 79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691819B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-d0083259c19e4c049c2e897761335378
출처 메모uspto-grants-2014_04