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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608609Generated: October 31, 2026

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

https://huagongshe.com/reaction/1608609

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 numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-11bc45c644d84b67a8ec4b84d9abf7bb
Source noteuspto-grants-1995_03