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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238645Generated: October 31, 2026

8-Methylimidazo(1,2-a)pyridine → 8-Methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/2238645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Methylimidazo(1,2-a)pyridineHCID 327957—
CatalystNickelHCID 935—
Solvent1-ButanolHCID 263—
Product8-Methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridineHCID 1044175879.9%

Reaction Conditions

Temperature65 °C

Reaction Steps

1 g of 8-methylimidazo[1,2-a]pyridine [3-1] was dissolved in 20 mL of 1-butanol, and a catalytic amount of Raney nickel of was added thereto. The mixture was stirred under a hydrogen atmosphere (5 atmospheric pressure) at 65° C. for 4 days. After cooling the reaction mixture back to room temperature, the insolubles were filtered through celite, and washed with methanol. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography, to obtain 823.3 mg of 8-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine [46-1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718801B2
Source datasetuspto-grants-2010_05
ORD IDord-8f3eeb8f5b18457c8a4ed2edf6b5570b
Source noteuspto-grants-2010_05