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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385571Generated: October 30, 2026

(5-(Benzyloxy)-4-(2-((tert-butoxycarbonyl)amino)ethoxy)pyridin-2-yl)methyl acetate → (4-(2-((Tert-butoxycarbonyl)amino)ethoxy)-5-hydroxypyridin-2-yl)methyl acetate

https://huagongshe.com/reaction/385571

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-(Benzyloxy)-4-(2-((tert-butoxycarbonyl)amino)ethoxy)pyridin-2-yl)methyl acetateHCID 57815373—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product(4-(2-((Tert-butoxycarbonyl)amino)ethoxy)-5-hydroxypyridin-2-yl)methyl acetateHCID 5781550870.5%

Reaction Steps

To a solution of 3.8 g of (5-(benzyloxy)-4-(2-((tert-butoxycarbonyl)amino)ethoxy)pyridin-2-yl)methyl acetate in 91 mL of ethanol, 1.1 g of 10% palladium carbon was added, and the mixture was stirred at room temperature for 5 hours under a hydrogen atmosphere. The insoluble substance was filtered off, and the solvent was distilled off under reduced pressure. Thereto were added chloroform and diethyl ether, and the solid was filtered off to obtain 2.1 g of (4-(2-((tert-butoxycarbonyl)amino)ethoxy)-5-hydroxypyridin-2-yl)methyl acetate as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-91ab084c0efb4c5cbb8ab031418a633e
Source noteuspto-grants-2013_02