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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731362Generated: November 3, 2026

HCID 20228695, compound → HCID 20228735, compound

https://huagongshe.com/reaction/1731362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20228695HCID 20228695—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20228735HCID 2022873563.6%

Reaction Steps

A solution of 5-(8-benzyloxy-3-methylimidazo[1,2-a]pyridin-2-yl)-3-methyl-2-benzoxazolinone (1.6 g) in a mixture of ethanol (200 ml) and tetrahydrofuran (100 ml) was hydrogenated over 10% palladium on carbon (wet, 0.5 g) under an atmospheric pressure of hydrogen at ambient temperature for an hour. The catalyst and an insoluble material were filtered off and the filtrate was evaporated in vacuo. The residue was recrystallized from a mixture of tetrahydrofuran and ethanol to give 5-(8-hydroxy-3-methylimidazo[1,2-a]pyridin-2-yl)-3-methyl-2-benzoxazolinone (0.78 g). mp. >280° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04621084
Source datasetuspto-grants-1986_11
ORD IDord-881a0eb97db44b7995636447c18dd973
Source noteuspto-grants-1986_11