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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286740Generated: October 25, 2026

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

https://huagongshe.com/reaction/2286740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantCysteamineHCID 6058—
ReactantSodium hydrideHCID 24758—
ReactantThiourea dioxideHCID 61274—
ReactantSodiumHCID 5360545—
Reactant2-aminoethanethiol DihydrochlorideHCID 10154133—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 665568—

Reaction Steps

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 (MgSO4) and evaporated to dryness to give 4-(2-aminoethyl)thiomethyl-5-methylimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04267337
Source datasetuspto-grants-1981_05
ORD IDord-6575deb9d3d24334bad58998b8e773a5
Source noteuspto-grants-1981_05