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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371282Generated: October 31, 2026

Acetic Acid → (S)-3-{(S)-4-Methyl-2-[2-(naphthalen-1-yloxy)-acetylamino]-pentanoylamino}-4-oxo-butyric acid

https://huagongshe.com/reaction/1371282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
Reactant(3 S)-3-[N-((1-naphthyloxy)acetyl)leucinyl]amino-4-oxobutanoic acid semicarbazoneHCID 178446027—
SolventFormaldehydeHCID 712—
SolventWaterHCID 962—
Product(S)-3-{(S)-4-Methyl-2-[2-(naphthalen-1-yloxy)-acetylamino]-pentanoylamino}-4-oxo-butyric acidHCID 982307479%

Reaction Steps

A solution of (3S)-3-[N-((1-naphthyloxy)acetyl)leucinyl]amino-4-oxobutanoic acid semicarbazone (0.320 g, 0.68 mmol) in 37% aqueous formaldehyde(1.0 mL)-acetic acid(1.0 mL)-methanol(3.0 mL) was stirred at room temperature under nitrogen for 3.5 hrs. The resulting solution was diluted with water and extracted with EtOAc. The extract was washed with water and saturated NaCl solution, dried over anhydrous Na2SO4 and evaporated to dryness. The residue was taken up in EtOAc, filtered through Celite and evaporated to dryness. The product was taken up in a small amount of dioxane, diluted with water, frozen and lyophilized to give the title compound (0.222 g, 79%) as a fluffy white solid. TLC(EtOAc-pyridine-AcOH-H2O; 60:20:5:10) Rf=0.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157430B2
Source datasetuspto-grants-2007_01
ORD IDord-f9f3d418cfa242729fd21b2b28cc085a
Source noteuspto-grants-2007_01