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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608608Generated: October 29, 2026

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

https://huagongshe.com/reaction/1608608

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 numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-eede9b486e8a4a14bc30dcc894b76cf1
Source noteuspto-grants-1995_03