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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730196Generated: October 26, 2026

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

https://huagongshe.com/reaction/1730196

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 numberUS03991200
Source datasetuspto-grants-1976_11
ORD IDord-c918647f07204f61a4b5a10fe41e0bad
Source noteuspto-grants-1976_11