Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260024Generated: November 1, 2026

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

https://huagongshe.com/reaction/1260024

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 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 numberUS08466282B2
Source datasetuspto-grants-2013_06
ORD IDord-9af3acb91191432cbc2b5c5c5242b88f
Source noteuspto-grants-2013_06