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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32464생성일: 2026년 10월 24일

N-(9-Fluorenylmethoxycarbonyloxy)succinimide → n-[(r)-2-[(9h-Fluoren-9-ylmethoxycarbonyl)(1-isopropyl-piperidin-4-ylmethyl)amino]-1-phenylethyl]carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/32464

반응식

참여 물질

역할이름HCID투입량
반응물N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
반응물N-[(R)-2-[(1-Isopropylpiperidin-4-ylmethyl)amino]-1-phenyl-ethyl]carbamic acid tert-butyl esterHCID 69307988—
생성물n-[(r)-2-[(9h-Fluoren-9-ylmethoxycarbonyl)(1-isopropyl-piperidin-4-ylmethyl)amino]-1-phenylethyl]carbamic acid tert-butyl esterHCID 69309681113.5%

반응 단계

Using coupling method B, N-[(R)-2-[(1-isopropylpiperidin-4-ylmethyl)amino]-1-phenylethyl]carbamic acid tert-butyl ester (1.1 g, 2.8 mmol) and 9-fluorenylmethyl N-succinimidyl carbonate (Fmoc-OSu, 962 mg, 2.9 mmol) afforded 1.9 g of the title compound as a crude residue, that was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427632B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-e4a11d44c2f74fedb928844e4d48c9a0
출처 메모uspto-grants-2008_09