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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615880Generated: October 31, 2026

Water → 4-(4-Chlorothiophen-2-yl)-1,3-thiazol-2-amine

https://huagongshe.com/reaction/1615880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThioureaHCID 2723790—
Reactant2-Acetyl-4-chlorothiopheneHCID 11105655—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventBromineHCID 24408—
Product4-(4-Chlorothiophen-2-yl)-1,3-thiazol-2-amineHCID 2303067845.6%

Reaction Steps

To a solution of 4.18 g of 4-chloro-2-acetylthiophene in 30 ml of diethylether, 1.5 ml of bromine was added under ice cooling, and the mixture was stirred at room temperature for 2 hours. Water was added to the reaction solution, and the organic phase was extracted. The obtained organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to obtain brominated compound. To a solution of the brominated compound in 30 ml of EtOH, 2.1 g of thiourea was added at room temperature, and the mixture was stirred at 80° C. overnight. The precipitate was filtered, and obtained solution was evaporated under reduced pressure. Chloroform was added and then an organic layer was washed with aqueous potassium carbonate and brine, and dried over sodium sulfate. The residue obtained by the evaporation of the solvent under reduced pressure was washed with hexane:EtOAc=1:1 to obtain 2.57 g of 2-amino-4-(4-chlorothiophen-2-yl)thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765764B2
Source datasetuspto-grants-2014_07
ORD IDord-3712e64fc75d434d890adbb2a3cc28d0
Source noteuspto-grants-2014_07