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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600256Generated: October 30, 2026

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

https://huagongshe.com/reaction/600256

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 (H) (23.7 g, 0.23 mol) and 2-bromo-1-(4-fluorophenyl)-ethanone (I) (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 (J) (43.0 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902192B2
Source datasetuspto-grants-2011_03
ORD IDord-9da37d17db9847e7a8317c54098562e8
Source noteuspto-grants-2011_03