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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824514Generated: October 25, 2026

2-[4-[4-Hydroxybut-1-ynyl]phenyl]-7-methylimidazo[1,2-a]pyridine → 2-[4-[4-Hydroxybutyl]phenyl]-7-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1824514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[4-[4-Hydroxybut-1-ynyl]phenyl]-7-methylimidazo[1,2-a]pyridineHCID 22015594—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-[4-[4-Hydroxybutyl]phenyl]-7-methylimidazo[1,2-a]pyridineHCID 2201565592.6%

Reaction Steps

The product of Step B, Example 33 (0.3 g) in ethanol (15 mL) was hydrogenated over 5% palladium on barium sulfate (0.06 g) for 4.5 hours. The reaction mixture was filtered and evaporated to afford the title compound (0.282 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041827B2
Source datasetuspto-grants-2006_05
ORD IDord-8311ef7cf0ee4daa9a5d1170dc0d2a14
Source noteuspto-grants-2006_05