Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462236Generated: October 25, 2026

1-[3-(Dimethylamino)propyl]piperazine → 2-{2-[4-(3-Dimethylaminopropyl)-1-piperazinyl]-5-thiadiazolyl}-1-methyl-5-nitroimidazole

https://huagongshe.com/reaction/462236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[3-(Dimethylamino)propyl]piperazineHCID 2736234—
Reactant2-(2-Chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazoleHCID 21390801—
Solvent1,4-DioxaneHCID 31275—
Product2-{2-[4-(3-Dimethylaminopropyl)-1-piperazinyl]-5-thiadiazolyl}-1-methyl-5-nitroimidazoleHCID 21390803—

Reaction Steps

A solution of 2-(2-chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazole in 200 ml. of dioxane is treated with 5.1 g. of 1-(3-dimethylaminopropyl)piperazine, and the mixture stirred at room temperature for 18 hours. The precipitate is collected, dissolved in 100 ml. of water, made alkaline with sodium hydroxide solution, and then extracted with 500 ml. of chloroform. The chloroform extract is dried and the solvent removed under reduced pressure. The yellow residue is recrystallized from 100 ml. of ethanol to give 2.9 g. of product, melting at 174°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04065567
Source datasetuspto-grants-1977_12
ORD IDord-c2bace9bd66849a0a94a28186d1478c3
Source noteuspto-grants-1977_12