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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379839Generated: October 29, 2026

Bromine → 2-Acetylaminomethyl-4-bromoacetylthiazole

https://huagongshe.com/reaction/2379839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant4-Acetyl-2-(acetylaminomethyl)thiazoleHCID 10012967—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Acetylaminomethyl-4-bromoacetylthiazoleHCID 18953911—

Reaction Conditions

Temperature70 °C

Reaction Steps

Bromine (2.2 g) was added slowly to a solution of 4-acetyl-2-acetylaminomethylthiazole (2.2 g) in acetic acid (20 ml) and water (20 ml), and the mixture was heated at 70° C. for 4 hours. The solvent was removed under reduced pressure to give crude product of 2-acetylaminomethyl-4-bromoacetylthiazole. The above residue was dissolved in ethanol (50 ml). Diaminomethylenethiourea (1.3 g) was added to the solution and the mixture was refluxed for 4 hours. The solvent was removed under reduced pressure. The residue was dissolved in water and then the solution was alkalized with a saturated aqueous potassium carbonate solution. The resulting precipitate was collected by filtration. The filtrate was extracted by ethyl acetate and then the solvent was removed under reduced pressure. The residue and the precipitate were chromatographed on an alumina column eluting with a mixture of chloroform and methanol (10:1). Recrystallization from water afforded 4-(2-acetylaminomethylthiazol-4-yl)-2-(diaminomethyleneamino)thiazole (430 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364871
Source datasetuspto-grants-1994_11
ORD IDord-1190bdf8f6d549199703275e92ef27c8
Source noteuspto-grants-1994_11