Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081722Generated: October 26, 2026

Triethylamine → 5-[3-(Phthalimido)propylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1081722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-3-BromopropylphthalimideHCID 21611—
ReactantHCID 178418687HCID 178418687—
SolventEthanolHCID 702—
Product5-[3-(Phthalimido)propylthio]imidazo[1,2-a]pyridineHCID 2336294171.1%

Reaction Steps

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (3.00 g, 20 mmoles) and N-[3-(bromo)propyl]phthalimide (5.90 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 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 4.79 g of the desired product (71.1%, colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587383
Source datasetuspto-grants-1996_12
ORD IDord-566c385a011a4d188b5d3a19881006c7
Source noteuspto-grants-1996_12