Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64402Generated: October 26, 2026

8-(benzyloxy)-N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide → N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/64402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-(benzyloxy)-N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-2-methylimidazo[1,2-a]pyridine-3-carboxamideHCID 86713410—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductN-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxamideHCID 8671340981.6%

Reaction Steps

To a solution of 5.2 g of 8-(benzyloxy)-N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide in 70 ml of ethanol was added 1.0 g of 10% palladium-carbon (wet), followed by stirring for 3 hours under a hydrogen atmosphere. The reaction mixture was filtered over Celite, the solvent was then evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography. To the obtained purified product were added hexane and diisopropyl ether, followed by stirring, and the resulting solid was collected by filtration and dried to obtain 3.5 g of N-[(1R)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-phenylethyl]-8-hydroxy-2-methylimidazo[1,2-a]pyridine-3-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447090B2
Source datasetuspto-grants-2016_09
ORD IDord-823888e42bcc4e1a9bffb8cb2a25fc5d
Source noteuspto-grants-2016_09