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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728200Generated: October 28, 2026

HCID 54000152, compound → HCID 15171525, compound

https://huagongshe.com/reaction/728200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54000152HCID 54000152—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 15171525HCID 1517152568.6%

Reaction Steps

A solution of 2-[2-(3-benzyloxy-4-nitrophenyl)vinyl]imidazo[1,2-a]pyridine (40 g) in ethanol (600 ml) was hydrogenated over 10% palladium on carbon (10 g) at 4 to 6 atmospheric pressure of hydrogen gas for 4 hours at 40° to 70° C. The catalyst was removed by filtration an the filtrate was evaporated in vacuo to give a crystalline residue, which was washed with diethyl ether and dried to give 2-[2-(4-amino-3-hydroxyphenyl)ethyl]-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine (19.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05047411
Source datasetuspto-grants-1991_09
ORD IDord-161b2af48e6f4e4997d37111f4f39ff5
Source noteuspto-grants-1991_09