Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634390Generated: October 31, 2026

Ethyl pyruvate → N-(Phenyl-furazan-3-yl)-D,L-alanine

https://huagongshe.com/reaction/1634390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl pyruvateHCID 12041—
Reactant4-Phenyl-1,2,5-oxadiazol-3-amineHCID 139132—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
ProductN-(Phenyl-furazan-3-yl)-D,L-alanineHCID 22312046—

Reaction Steps

4-Phenyl-furazan-3-ylamine (Maybridge) and ethyl pyruvate (Aldrich) were dissolved in dry ethanol. Platinum on sulfide carbon (5%) was added and the resulting mixture was hydrogenated (1000 psi, H2) at 150° C. for 8 hours. The reaction mixture was then filtered through Celite and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography using CHCl3 as the eluant to provide the title compound as its ethyl ester. The ethyl ester was then hydrolyzed using General Procedure II-A, Method B (LiOH/H2O/dioxane) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506782B1
Source datasetuspto-grants-2003_01
ORD IDord-d1783252934642fab14a64c83d46719f
Source noteuspto-grants-2003_01