戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 261096作成日:2026年10月27日

Dimethyl Sulfoxide → 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole

https://huagongshe.com/reaction/261096

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物CysteamineHCID 6058—
反応物Sodium hydrideHCID 24758—
反応物Thiourea dioxideHCID 61274—
反応物SodiumHCID 5360545—
反応物2-aminoethanethiol DihydrochlorideHCID 10154133—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 66556845%

反応手順

Triphenyl β-acetylvinylphosphonium bromide (4.11 g, 0.01 mole) was added in one portion to a stirred suspension of 1.1 g (0.01 mole) of formamidine sulfinic acid in 20 ml of dimethylsulfoxide containing 0.25 g of sodium hydride. The mixture was stirred at ambient temperature for 1 hour then at 80° for an additional hour. A solution of 0.99 g (0.01 mole) of the sodium salt of cysteamine, prepared by addition of two equivalents of sodium methoxide to cysteamine dihydrochloride, in 10 ml of methanol was added and the resulting mixture was heated at 70°-80° for 4 hours. The mixture was diluted with twice its volume of water and the triphenyl phosphine was removed by filtration. The filtrate was extracted with 100 ml of toluene and with two 100 ml portions of chloroform. The chloroform extracts were combined, dried and evaporated to dryness to give 4-(2-aminoethyl)thiomethyl-5-methylimidazole in 45% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04163858
出典データセットuspto-grants-1979_08
ORD IDord-77e8e0a94005434c9bcf97a7ff593841
出典メモuspto-grants-1979_08