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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033043Generated: October 31, 2026

Benzoyl chloride → 4-(5-Acetylaminomethylfuran-2-yl)-2-(3-benzoylthioureido)thiazole

https://huagongshe.com/reaction/1033043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium thiocyanateHCID 15666—
Reactant150208-26-7HCID 7064095—
SolventAcetoneHCID 180—
Product4-(5-Acetylaminomethylfuran-2-yl)-2-(3-benzoylthioureido)thiazoleHCID 10692374—

Reaction Steps

Benzoyl chloride (2.67 ml) was dropped to a refluxing solution of ammonium thiocyanate (1.92 g) in acetone (50 ml) and the mixture was refluxed for 15 minutes. 4-(5-Acetylaminomethylfuran-2-yl)-2-aminothiazole (5.20 g) was added portionwise to the refluxing mixture. After the mixture was refluxed for further two hours, the solvent was evaporated in vacuo and the residue was mixed with water and ethyl acetate. The resulting precipitate was collected by filtration and washed with ethyl acetate to afford 4-(5-acetylaminomethylfuran-2-yl)-2-(3-benzoylthioureido)thiazole (5.50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308857
Source datasetuspto-grants-1994_05
ORD IDord-0116f2f87fcd4d84a341fdcc19af44b4
Source noteuspto-grants-1994_05