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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751479Generated: October 28, 2026

N-Methoxycarbonyl-2-phenylglycine → Methyl (S)-1-((S)-2-(5-(4'-(2-((1R,3S,4S)-2-((S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetyl)-2-azabicyclo[2.2.1]heptan-3-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamate

https://huagongshe.com/reaction/1751479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxycarbonyl-2-phenylglycineHCID 596264—
Reactant2-(tert-Butoxycarbonyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acidHCID 15056388—
Reactant1-((Tert-butoxy)carbonyl)-4,4-difluoropyrrolidine-2-carboxylic acidHCID 23512514—
Reactant2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic acidHCID 58516241—
Reactant(S)-benzyl 2-(5-(2-bromonaphthalen-6-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylateHCID 70653414—
ReactantHCID 86708747HCID 86708747—
ProductMethyl (S)-1-((S)-2-(5-(4'-(2-((1R,3S,4S)-2-((S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetyl)-2-azabicyclo[2.2.1]heptan-3-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamateHCID 86708751—

Reaction Steps

The title compound was prepared as described for {2-[4,4-Difluoro-2-(5-{4-[6-(2-{1-[2-methoxycarbonylamino-2-(tetrahydro-pyran-4-yl)-acetyl]-pyrrolidin-2-yl}-3H-imidazol-4-yl)-naphthalen-2-yl]-phenyl}-1H-imidazol-2-yl)-pyrrolidin-1-yl]-2-oxo-1-phenyl-ethyl}-carbamic acid methyl ester, substituting (S)-benzyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate for (S)-benzyl 2-(5-(6-bromonaphthalen-2-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate, 2-Azabicyclo[2.2.1]heptane-2,3-dicarboxylic acid 2-tert-butyl ester for 4,4-Difluoro-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester, and Methoxycarbonylamino-(tetrahydro-pyran-4-yl)-acetic acid for Methoxycarbonylamino-phenyl-acetic acid. LCMS-ESI+: calculated for C44H55N8O7: 807.4; observed [M+1]+: 807.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-82c078b321704c85b165ad1fa801bba0
Source noteuspto-grants-2015_10