HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1112020Erstellt: 26. Oktober 2026
Dimethyl Sulfoxide → 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole
https://huagongshe.com/reaction/1112020
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Cysteamine | HCID 6058 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Thiourea dioxide | HCID 61274 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | 2-aminoethanethiol Dihydrochloride | HCID 10154133 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole | HCID 665568 | — |
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 (MgSO4) and evaporated to dryness to give 4-(2-aminoethyl)thiomethyl-5-methylimidazole.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04119781 |
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| Quelldatensatz | uspto-grants-1978_10 |
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| ORD ID | ord-cb1ee3e0d85f49028f59fb31004d75d9 |
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| Quellennotiz | uspto-grants-1978_10 |
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