HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287186Generated: November 1, 2026
Cysteamine Hydrochloride → 2-(((5-Methyl-1H-imidazol-4-yl)methyl)thio)ethylamine dihydrochloride
https://huagongshe.com/reaction/1287186
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cysteamine Hydrochloride | HCID 9082 | — |
| Reactant | 4-Methylimidazol-5-ylmethanolhydrochloride | HCID 3084707 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-(((5-Methyl-1H-imidazol-4-yl)methyl)thio)ethylamine dihydrochloride | HCID 3015999 | — |
Reaction Steps
A solution of 4-hydroxymethyl-5-methylimidazole hydrochloride (30.0 g) and cysteamine hydrochloride (23.0 g) in acetic acid (200 ml) was heated under reflux for 10 hours. Following cooling to 15°-20°, the solid which crystallised was collected and washed with isopropyl alcohol to give 4-methyl-5-[(2-aminoethyl)thiomethyl]imidazole dihydrochloride m.p. 189°-192°. Potassium carbonate (7.75 g) was added to a solution of 4-methyl-5-[(2-aminoethyl)thiomethyl]imidazole dihydrochloride (14.6 g) in water (120 ml). The solution was stored at room temperature for 15 minutes and methyl isothiocyanate (5.15 g) was added. After heating under reflux for 30 minutes, the solution was slowly cooled to 5°. The product was collected and recrystallised from water to give N-methyl-N'-[2-((5-methyl-4-imidazolyl)methylthio)ethyl]thiourea, m.p.150°-152°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03984293 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-3d6ee36469bf406f9a917cb439cd8246 |
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| Source note | uspto-grants-1976_10 |
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