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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783831Generated: October 31, 2026

2-Aminothiazole → HCID 57433652, compound

https://huagongshe.com/reaction/1783831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-(2-Bromoacetyl)benzonitrileHCID 2735867—
SolventEthanolHCID 702—
ProductHCID 57433652HCID 5743365281%

Reaction Steps

To a mixture of 2-aminothiazole (3.29 g, 32.9 mmol) and 2-bromo-3′-cyano-acetophenone (7.37 g, 32.9 mmol) was added absolute ethanol (250 mL). The reaction was allowed to reflux with vigorous stirring for 20 hours. The reaction mixture was reduced to half its original volume in vacuo. The remaining suspension was poured onto ice-water (200 mL) and the resulting mixture was basified by addition of ammonium hydroxide solution (30%, 100 mL). Product was collected by filtration and washed with water (50 mL), dried in a vacuum oven at 50° C. to provide 6-(3-cyanophenyl)-imidazo[2,1-b]thiazole (6.0 g, 81%). It was used with out further purification. LCMS: 226 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501430B2
Source datasetuspto-grants-2009_03
ORD IDord-d81fd74075da410cb9bfee6494225657
Source noteuspto-grants-2009_03