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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49710Generated: October 30, 2026

Ammonium formate → (RS) Methyl 3-{6-[2-(4-amino-3-hydroxy-phenyl)-acetylamino]-pyridin-3-yl}-butyrate

https://huagongshe.com/reaction/49710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant(RS) methyl 3-{6-[2-(3-hydroxy-4-nitrophenyl)-acetylamino]-pyridin-3-yl}-butanoateHCID 17946660—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(RS) Methyl 3-{6-[2-(4-amino-3-hydroxy-phenyl)-acetylamino]-pyridin-3-yl}-butyrateHCID 1794666680.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

Ammonium formate (1.7 g) and 10% palladium on charcoal were added to a solution of (RS) methyl 3-{6-[2-(3-hydroxy-4-nitrophenyl)-acetylamino]-pyridin-3-yl}-butanoate (180 mg, Reference Example 15) in ethanol (15 mL). The mixture was stirred at 60° C. for 1 hour, then cooled to room temperature and then filtered through a pad of diatomaceous earth. The filter pad was washed with ethanol. The combined filtrate and washings were evaporated and the residue was dissolved in ethyl acetate. This solution was washed with water, then dried over magnesium sulphate and then evaporated to give the title compound (134 mg) as a pale brown oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706738B2
Source datasetuspto-grants-2004_03
ORD IDord-4bb36f5b667c4fed8088862929155d19
Source noteuspto-grants-2004_03