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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184199Generated: October 31, 2026

Diphenyl sulfide → Ethyl 3-(4-methoxybutyl)imidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/1184199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl sulfideHCID 8766—
Reactantethyl 3-[(1E)-4-methoxybut-1-en-1-yl]imidazo[1,2-a]pyridine-2-carboxylateHCID 58355141—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(4-methoxybutyl)imidazo[1,2-a]pyridine-2-carboxylateHCID 5835556148.7%

Reaction Steps

Ethyl 3-[(1E)-4-methoxybut-1-en-1-yl]imidazo[1,2-a]pyridine-2-carboxylate (530 mg) and diphenyl sulfide (3.6 mg) were dissolved in ethyl acetate (13 ml), 10% palladium carbon (50% in water) (53 mg) was added and the mixture was stirred in a hydrogen stream at ambient temperature and normal pressure for 2.5 hr. The catalyst was filtered off, and the to filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate was concentrated under reduced pressure to give the object product (260 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664380B2
Source datasetuspto-grants-2014_03
ORD IDord-30789a064d5c474bbe193cf12ef89f39
Source noteuspto-grants-2014_03