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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322040Generated: October 26, 2026

Hydrochloric Acid → 2-Benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1-[[2'-(aminomethyl)[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]propanamide, hydrochloride

https://huagongshe.com/reaction/322040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetra-hydro-4-oxo-1-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]-propanamideHCID 20641419—
SolventMethanolHCID 887—
Product2-Benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1-[[2'-(aminomethyl)[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]propanamide, hydrochlorideHCID 131722473—

Reaction Steps

To a solution of of 2-benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1-[[2′-[(t-butoxycarbonylamino)methyl][1,1′-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]propanamide (Step H) in methanol is added 9N aqueous hydrochloric acid. The reaction mixture is stirred overnight at room temperature then the solvent is removed under vacuum. The resulting oil is dissolved in methanol and the solvent is removed under vacuum to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211174B1
Source datasetuspto-grants-2001_04
ORD IDord-a1aba9dea2c448f69284bb84b08e3918
Source noteuspto-grants-2001_04