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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Cysteamine | HCID 6058 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Thiourea dioxide | HCID 61274 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-aminoethanethiol Dihydrochloride | HCID 10154133 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04267337 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-6575deb9d3d24334bad58998b8e773a5 |
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| Source note | uspto-grants-1981_05 |
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