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HRID 462236作成日:2026年10月26日

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

https://huagongshe.com/reaction/462236

反応式

関与物質

役割名称HCID仕込み量
反応物1-[3-(Dimethylamino)propyl]piperazineHCID 2736234—
反応物2-(2-Chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazoleHCID 21390801—
溶媒1,4-DioxaneHCID 31275—
生成物2-{2-[4-(3-Dimethylaminopropyl)-1-piperazinyl]-5-thiadiazolyl}-1-methyl-5-nitroimidazoleHCID 21390803—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04065567
出典データセットuspto-grants-1977_12
ORD IDord-c2bace9bd66849a0a94a28186d1478c3
出典メモuspto-grants-1977_12