Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5437Generated: October 28, 2026

1-Bromo-3-chloropropane → 5-[3-(Chloro)propylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/5437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantTriethylamineHCID 8471—
ReactantHCID 178418687HCID 178418687—
SolventEthanolHCID 702—
Product5-[3-(Chloro)propylthio]imidazo[1,2-a]pyridineHCID 2336288172.1%

Reaction Steps

To a suspension of 5-mercaptoimidazo[1,2-a]pyridine (5.02 g, 33.4 mmoles) and 1-bromo-3-chloropropane (5.26 g, 33.4 mmoles) in ethanol (100 ml) was added triethylamine (4.66 ml, 33.4 mmoles) and the mixture was stirred at room temperature for 17 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) to obtain 5.46 g of the desired product (72.0%, light brown oily product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-877f58037d2241b39b1ba3a388bcb737
Source noteuspto-grants-1993_09