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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081724Generated: November 3, 2026

Triethylamine → 5-[6-(Phthalimido)hexylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(6-Bromohexyl)phthalimideHCID 141120—
ReactantHCID 178418687HCID 178418687—
SolventEthanolHCID 702—
Product5-[6-(Phthalimido)hexylthio]imidazo[1,2-a]pyridineHCID 1995699875.5%

Reaction Steps

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (1.50 g, 10 mmoles) and N-[6-(bromo)hexyl]phthalimide (3.10 g, 10 mmoles) in ethanol (100 ml) was added triethylamine (2.1 ml, 15 mmoles) and the mixture was stirred at room temperature for 12 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 2.86 g of the desired product (75.5%, light tan solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-e07c2d671bc1416f84fcaa97ebed6736
Source noteuspto-grants-1996_12