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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163518Generated: October 26, 2026

Pyridine → 2-Bromo-4-chloroacetamidothiazole

https://huagongshe.com/reaction/2163518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium AcetateHCID 517045—
Reactant2-Bromo-1,3-thiazol-4-amineHCID 20294042—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-chloroacetamidothiazoleHCID 2029403329.7%

Reaction Steps

The starting material was prepared as follows. 4-Amino-2-bromothiazole (15.6 g) and chloroacetyl chloride (7.6 g) were suspended in methylene chloride (100 ml) with stirring and treated with pyridine (16 ml) over 15 min., maintaining reaction temperature at 0° C. with an ice bath. After the addition was complete, the reaction mixture was stirred at room temperature for 3 hours, then poured onto 20% aqueous sodium acetate (500 ml) and stirred for 30 minutes. The mixture was separated and the organic layer washed with 2N hydrochloric acid, water, sodium carbonate solution and water. The organic layer was dried (MgSO4) and the solvent removed in vacuo and the residue recrystallised twice from carbon tetrachloride to give 2-bromo-4-chloroacetamidothiazole (5.1 g). m.p. 146°-8° C. (Found: C, 24.1; H, 1.7; N, 11.2. C5H4ClBrN2OS requires C, 23.5; H, 1.6; N, 11.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134984
Source datasetuspto-grants-1979_01
ORD IDord-b37682b65571438395ad71d0a04b2d08
Source noteuspto-grants-1979_01