Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5452Generated: October 26, 2026

Triethylamine → 5-[4-(Phthalimido)butylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/5452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(4-Bromobutyl)phthalimideHCID 93575—
ReactantHCID 178418687HCID 178418687—
SolventEthanolHCID 702—
Product5-[4-(Phthalimido)butylthio]imidazo[1,2-a]pyridineHCID 2336287164.1%

Reaction Steps

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (3.00g, 20 mmoles) and N-[4-(bromo)butyl]phthalimide (6.21 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 and heated at reflux for 45 minutes. After the solvent was distilled off, chloroform was added to the residue, which was washed with saturated saline, dried over anhydrous magnesium sulfate and the solvent was distilled off. Then, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 4.50 g of the desired product (64.1%, pale yellow crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-50be1fc82c544b38bf6a4a6ff7e52623
Source noteuspto-grants-1993_09