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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081725Generated: November 2, 2026

Triethylamine → 5-[2-[2-(Phthalimido)ethyloxy]ethylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(2-(2-bromoethoxy)ethyl)-2,3-dihydro-1H-isoindole-1,3-dioneHCID 13028611—
ReactantHCID 178418687HCID 178418687—
SolventEthanolHCID 702—
Product5-[2-[2-(Phthalimido)ethyloxy]ethylthio]imidazo[1,2-a]pyridineHCID 2336290354.5%

Reaction Steps

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (3.00 g, 20 mmoles) and N-[2-[2-(bromo)ethyloxy]ethyl]phthalimide (5.96 g, 20 mmoles) in ethanol (200 ml) was added triethylamine (4.2 ml, 30 mmoles) and the mixture was stirred at room temperature for 12 hours and heated at reflux for 3 hours. After the solvent was distilled off, chloroform was added to the residue, which was washed with water, dried over anhydrous magnesium sulfate and the solvent was distilled off. Then, the residue was purified by column chromatography (eluent:ethyl acetate) to obtain 4.00 g of the desired product (54.5%, light tan solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-85766a43882944b6a87496b14444f38e
Source noteuspto-grants-1996_12