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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033048Generated: October 25, 2026

N-{[5-(2-chloroacetyl)furan-2-yl]methyl}acetamide → 4-(5-Acetylaminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazole

https://huagongshe.com/reaction/1033048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-{[5-(2-chloroacetyl)furan-2-yl]methyl}acetamideHCID 2393628—
ReactantAmidinothioureaHCID 2724563—
SolventEthanolHCID 702—
Product4-(5-Acetylaminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazoleHCID 1177836646.6%

Reaction Steps

A solution of 5-acetylaminomethyl-2-chloroacetylfuran (39.9 g) and diaminomethylenethiourea (21.9 g) in ethanol (400 ml) was refluxed for two hours with stirring. The solvent was evaporated in vacuo and the residue was dissolved in water (300 ml). The solution was basified with an aqueous potassium carbonate. The resulting precipitate was collected by filtration, washed with water and recrystallized from a mixture of methanol, tetrahydrofuran and diisopropyl ether to afford 4-(5-acetylaminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazole (24.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308857
Source datasetuspto-grants-1994_05
ORD IDord-8a22acb0dcf145649c406210ab4bf3a1
Source noteuspto-grants-1994_05