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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751433Generated: October 28, 2026

(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid → HCID 178502332, compound

https://huagongshe.com/reaction/1751433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acidHCID 59540170—
ReactantHCID 178502334HCID 178502334—
ProductHCID 178502332HCID 178502332—

Reaction Steps

Title compound was prepared by methods analogous to those described for methyl (S)-1-((S)-2-(7-(4-(2-((1R,3S,4S)-2-((2S,3R)-2-methoxycarbonylamino-3-methoxybutanoyl)-2-azabicyclo[2.2.1]heptan-3-yl)-1H-imidazol-5-yl)phenyl)-1H-naphtho[1,2-d]imidazol-2-yl)pyrrolidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamate, substituting (S)-2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic acid for (2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid. (ESI) m/z 831 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-852dc592a2f84638b8c9d63a9959cd96
Source noteuspto-grants-2015_10