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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322041Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-benzyloxycarbonylamino-3-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1H-naphtho[2,1-b]azepin-3(R)-yl]butanamideHCID 20641421—
Reactant2'-[(t-Butoxycarbonylamino)methyl]-1,1-biphenyl-4-methanolHCID 22008472—
Product3-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—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211174B1
Source datasetuspto-grants-2001_04
ORD IDord-42dc8f2981ef4db187b6a59d56bd0aa6
Source noteuspto-grants-2001_04