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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322041생성일: 2026년 10월 25일

3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamide → 3-Benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetra-hydro-4-oxo-5-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]-butanamide

https://huagongshe.com/reaction/322041

반응식

참여 물질

역할이름HCID투입량
반응물3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamideHCID 20641421—
반응물2'-[(t-Butoxycarbonylamino)methyl]-1,1-biphenyl-4-methanolHCID 22008472—
생성물3-Benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetra-hydro-4-oxo-5-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]-butanamideHCID 20641423—

반응 단계

The product of Step B is prepared from 3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamide (Step A) and 2′-[(t-butoxycarbonylamino)methyl]-1,1′-biphenyl-4-methanol, methanesulfonate ester (Example 1, Step G) according to the procedure for Example 1, Step H.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211174B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-42dc8f2981ef4db187b6a59d56bd0aa6
출처 메모uspto-grants-2001_04