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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261096Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/261096

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktCysteamineHCID 6058—
EduktSodium hydrideHCID 24758—
EduktThiourea dioxideHCID 61274—
EduktSodiumHCID 5360545—
Edukt2-aminoethanethiol DihydrochlorideHCID 10154133—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 66556845%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04163858
Quelldatensatzuspto-grants-1979_08
ORD IDord-77e8e0a94005434c9bcf97a7ff593841
Quellennotizuspto-grants-1979_08