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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCysteamine HydrochlorideHCID 9082—
Reactant4-Methylimidazol-5-ylmethanolhydrochlorideHCID 3084707—
SolventAcetic AcidHCID 176—
Product2-(((5-Methyl-1H-imidazol-4-yl)methyl)thio)ethylamine dihydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03984293
Source datasetuspto-grants-1976_10
ORD IDord-3d6ee36469bf406f9a917cb439cd8246
Source noteuspto-grants-1976_10