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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925215Generated: November 1, 2026

2-Aminothiazole → 6-(4-Fluorophenyl)imidazo[2,1-b][1,3]thiazole

https://huagongshe.com/reaction/1925215

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Bromo-1-(4-fluorophenyl)ethan-1-oneHCID 96749—
SolventEthanolHCID 702—
Product6-(4-Fluorophenyl)imidazo[2,1-b][1,3]thiazoleHCID 86819886%

Reaction Steps

To a mixture of 2-aminothiazole (23.7 g, 0.23 mol) and 2-bromo-4′-fluoroacetophenone (alternatively named: 2-bromo-1-(4-fluorophenyl)-ethanone) (50 g, 0.23 mol) is added absolute ethanol (600 ml). The reaction is allowed to reflux with vigorous stirring for 16 hours. The reaction mixture is reduced to half its original volume in vacuo. The remaining liquid is poured onto ice and the solution made basic by the addition of ammonium hydroxide solution (30%). The resulting fine solid is filtered and washed with water. The dark yellow solid so obtained is dried in a vacuum oven at 50° C. to provide 6-(4-fluorophenyl)-imidazo[2,1-b]thiazole (43.0 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178672B2
Source datasetuspto-grants-2012_05
ORD IDord-5e81ded710324c1ead31e5ea481fc1c1
Source noteuspto-grants-2012_05