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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058331Generated: October 25, 2026

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

https://huagongshe.com/reaction/2058331

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 numberUS04215217
Source datasetuspto-grants-1980_07
ORD IDord-a5226e266457499294ccd0db79a13a7d
Source noteuspto-grants-1980_07