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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081720Generated: October 25, 2026

Triethylamine → 5-(Phthalimidomethylthio)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-HCID 79244—
ReactantHCID 178418687HCID 178418687—
SolventEthanolHCID 702—
Product5-(Phthalimidomethylthio)imidazo[1,2-a]pyridineHCID 2336286469.4%

Reaction Steps

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (3.00 g, 20 mmoles) and N-bromomethylphthalimide (5.28 g, 22 mmoles) in ethanol (200 ml) was added triethylamine (4.2 ml, 30 mmoles) and the mixture was stirred at room temperature for 1 hour. 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 4.29 g of the desired product (69.4%, pale yellow crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-c57c98a354744f8c9454cf2b026a4a06
Source noteuspto-grants-1996_12