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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5473Generated: October 29, 2026

Triethylamine → HCID 23363004, compound

https://huagongshe.com/reaction/5473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-[2-(Bromo)ethyl]isoindolin-1-oneHCID 14624177—
ReactantHCID 178418687HCID 178418687—
SolventEthanolHCID 702—
ProductHCID 23363004HCID 2336300477%

Reaction Steps

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (150 mg, 1 mmole) and 2-[2-(bromo)ethyl]isoindolin-1-one (240 mg, 1 mmole) in ethanol (15 ml) was added triethylamine (0.21 ml, 1.5 mmoles) and the mixture Was stirred at room temperature for 12 hours and heated at reflux for 2 hours. After the solvent was distilled off, chloroform was added to the residue which was washed with water and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography [eluent: ethyl acetate/ethanol (15:1)] to obtain 238 mg of the desired product (77.0%, light brown solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-3bef49f4277949b99b8d263b16800965
Source noteuspto-grants-1993_09