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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573021Generated: October 28, 2026

4-Oxobutanoic acid → HCID 66548074, compound

https://huagongshe.com/reaction/573021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Oxobutanoic acidHCID 1112—
Reactant1,4-DioxaneHCID 31275—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86678358HCID 86678358—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 66548074HCID 66548074—

Reaction Steps

17.1 mg (18 μmol) N-methyl-L-valyl-N-[(3R,4S,5S)-3-methoxy-1-{(2S)-2-[(1R,2R)-1-methoxy-2-methyl-3-oxo-3-{[(1R)-2-phenyl-1-(5-phenyl-1,3,4-oxadiazol-2-yl)ethyl]-amino}propyl]pyrrolidin-1-yl}-5-methyl-1-oxoheptan-4-yl]-N-methyl-L-valinamide trifluoroacetic acid salt (intermediate 22) was dissolved in 0.6 mL dioxane/water (1:1) and reacted with a 15% aqueous solution of 4-oxobutanoic acid in the presence of sodium cyanoborohydride in a process similar to the synthesis process in Example 1. After lyophilization from dioxane, 14.8 mg (89% of the theoretical) of the title compound was obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029406B2
Source datasetuspto-grants-2015_05
ORD IDord-b1a7af7167944419ad2e7763bb1e857e
Source noteuspto-grants-2015_05