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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5451Generated: October 25, 2026

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

https://huagongshe.com/reaction/5451

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 (3.00g, 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 numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-2142af33e93641faaf0996e15f201439
Source noteuspto-grants-1993_09