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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1254511생성일: 2026년 10월 27일

Piperidine → (S)-2-amino-3-(4-tert-butoxyphenyl)-N-((S)-1,1-diethoxypropan-2-yl)-N-(naphthalen-1-ylmethyl)propanamide

https://huagongshe.com/reaction/1254511

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물(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 86698526—
생성물(S)-2-amino-3-(4-tert-butoxyphenyl)-N-((S)-1,1-diethoxypropan-2-yl)-N-(naphthalen-1-ylmethyl)propanamideHCID 6707524299.5%

반응 단계

According to the procedure described in the synthesis method of Compound IV-1, (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 (Compound III-2) 1.34 g (1.84 mmol) was treated with piperidine and purified on silica gel column chromatography (n-hexane:ethyl acetate=9:1, chloroform:methanol=100:0 and 8:2) to obtain the title compound 928 mg (99%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08455488B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-c8a63030cc49415293a7934a7efbc207
출처 메모uspto-grants-2013_06