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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1033429생성일: 2026년 10월 27일

3-t-butoxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]butanamide → 3-[[1-[[2'-nitrophenoxy-[1,1'-biphenyl]-4-yl]methyl]-2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]amino]-1,1-dimethyl-3-oxopropylcarbamic acid, 1,1-dimethyethyl ester

https://huagongshe.com/reaction/1033429

반응식

참여 물질

역할이름HCID투입량
반응물3-t-butoxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]butanamideHCID 10474604—
반응물4'-Bromoethyl-2-(4-nitrophenoxy)-1,1'-biphenylHCID 54141217—
생성물3-[[1-[[2'-nitrophenoxy-[1,1'-biphenyl]-4-yl]methyl]-2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]amino]-1,1-dimethyl-3-oxopropylcarbamic acid, 1,1-dimethyethyl esterHCID 131718402—

반응 단계

Prepared from 4'-bromoethyl-2-(4-nitrophenoxy) -1,1'-biphenyl and 3-t-butoxycarbonylamino-3-methyl -N-[2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3-(R) -yl]-butanamide (Example 57, Step A) by the procedure described in Example 69, Step D. 1NMR (200 MHz, CDCl3): 1.32 (s,6H), 1.38 (s,9H), 1.78 (m,1H), 2.3-2.7 (m,5H), 4.47 (m,1H), 4.75 (d,15 Hz,1H), 5.13 (d,15 Hz,1H), 6.63 (d,7 Hz,1H), 6.75 (d,8 Hz,2H), 7.05-7.50 (m,/11H), 7.97 (s,1H), 7.98 (d,8 Hz,2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05310737
출처 데이터셋uspto-grants-1994_05
ORD IDord-a730f94af2f147009082b756213500c8
출처 메모uspto-grants-1994_05