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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573018Generated: October 31, 2026

4-Oxobutanoic acid → HCID 66547906, compound

https://huagongshe.com/reaction/573018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Oxobutanoic acidHCID 1112—
Reactant1,4-DioxaneHCID 31275—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86678362HCID 86678362—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 66547906HCID 66547906—

Reaction Steps

15.5 mg (10 μmol) N-methyl-L-valyl-N-[(3R,4S,5S)-1-{(2S)-2-[(1R,2R)-3-{[(2S,3E)-1,4-diphenylbut-3-en-2-yl]amino}-1-methoxy-2-methyl-3-oxopropyl]pyrrolidin-1-yl}-3-methoxy-5-methyl-1-oxoheptan-4-yl]-N-methyl-L-valinamide trifluoroacetic acid salt (intermediate 19) was dissolved in 1.0 mL dioxane/water (1:1) and reacted with a 15% aqueous solution of 4-oxobutanoic acid in the presence of sodium cyanoborohydride, by analogy with the synthesis in Example 1. After lyophilization from dioxane, 10.3 mg (68% 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-e9e0074ab90b414cb06c52a42d077fd2
Source noteuspto-grants-2015_05