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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608604Generated: October 26, 2026

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

https://huagongshe.com/reaction/1608604

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 numberUS05395839
Source datasetuspto-grants-1995_03
ORD IDord-aa89be8d96504f4cb91fb287211e894a
Source noteuspto-grants-1995_03