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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1033428생성일: 2026년 10월 26일

3-t-butoxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-2-oxo-1H-benzazepin-3(R)-yl]butanamide → N-[1-[[(2'-Acetoxy)[1,1'-biphenyl]-4-yl]methyl]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3(R)-yl]-3-t-butoxycarbonylamino-3-methylbutanamide

https://huagongshe.com/reaction/1033428

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'-Bromomethyl-2-acetoxy-1,1'-biphenylHCID 21836594—
생성물N-[1-[[(2'-Acetoxy)[1,1'-biphenyl]-4-yl]methyl]-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-3(R)-yl]-3-t-butoxycarbonylamino-3-methylbutanamideHCID 22877467—

반응 단계

Prepared from 4-'-bromomethyl-2-acetoxy-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. 1H NMR (200 MHz, CDCl3): 1.38 (s,6H), 1.45 (s,9H), 1.85 (m,1H), 2.02 (s,3H), 2.35-2.65 (m,5H), 4.52 (m,1H), 4.84 (d,15 Hz,1H), 5.30 (d,15 Hz,1H), 6.71 (d,7 Hz,1H), 7.1-7.4 (m, 12 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05310737
출처 데이터셋uspto-grants-1994_05
ORD IDord-c341ac0138b84df0b15ac961afe80893
출처 메모uspto-grants-1994_05