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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728145Generated: October 30, 2026

HCID 67836422, compound → HCID 15684647, compound

https://huagongshe.com/reaction/728145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67836422HCID 67836422—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
ProductHCID 15684647HCID 1568464762.8%

Reaction Steps

A solution of 2-[2-(3-benzyloxy-4-nitrophenyl)vinyl]-7-ethoxy-3-methylimidazo[1,2-a]pyridine (3.8 g) in N,N-dimethylformamide (80 ml) was subjected to catalytic reduction over 10% palladium on carbon (1.9 g) under atmospheric pressure of hydrogen gas at 40° to 60° C. for hours. The catalyst was removed by filtration and the filtrate was evaporated in vacuo. The residue was triturated with a mixture of diethyl ether and diisopropyl ether and the precipitate was collected by filtration to give 2-[2-(4-amino-3-hydroxyphenyl)ethyl]-7-ethoxy-3-methylimidazo[1,2-a]pyridine (1.73 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05047411
Source datasetuspto-grants-1991_09
ORD IDord-1d2b97bf4d524af2a7a5fe2793fc2358
Source noteuspto-grants-1991_09