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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113287Generated: October 26, 2026

Hydrochloric Acid → 2-Bromoimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/2113287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5-Bromo-2-formylaminomethylthiazoleHCID 23088762—
SolventTolueneHCID 1140—
Product2-Bromoimidazo[5,1-b]thiazoleHCID 1046546860.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

Toluene (1.0 L) was added to 104 g of 5-bromo-2-formylaminomethylthiazole, and the mixture was heated to 90° C. and was stirred. A solution of 65.8 g of phosphorus oxychloride in 100 ml of toluene was added to the reaction mixture, and the mixture was stirred at that temperature for 1.5 hr. After standing to cool, 2 L of a 0.5 N aqueous hydrochloric acid solution was added, and the aqueous layer was separated. The aqueous layer was adjusted to pH 6.2 by the addition of a 5 N aqueous sodium hydroxide solution and was extracted with 1.5 L of ethyl acetate and then with 1.0 L of ethyl acetate. The organic layers were combined, were washed with a 5% aqueous sodium bicarbonate solution and a 20% aqueous sodium chloride solution in that order, and were dried over anhydrous magnesium sulfate. The solvent was removed to bring the volume to about 100 ml, 500 ml of ethyl acetate:hexane=1:4 solution was added thereto, and the mixture was stirred in an ice-water bath for crystallization to give 57.6 g of 2-bromimidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524951B2
Source datasetuspto-grants-2009_04
ORD IDord-64c5115226264193a440122c238141f9
Source noteuspto-grants-2009_04