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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333718Generated: October 26, 2026

2-Amino-6-benzothiazolol → 2-(4-Nitrophenyl)imidazo[2,1-b]benzothiazol-7-ol

https://huagongshe.com/reaction/333718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-6-benzothiazololHCID 33462—
Reactant2-Bromo-4'-nitroacetophenoneHCID 66840—
CatalystTetrabutylammonium IodideHCID 67553—
SolventEthanolHCID 702—
Product2-(4-Nitrophenyl)imidazo[2,1-b]benzothiazol-7-olHCID 29933257—

Reaction Steps

2-Amino-6-hydroxybenzothiazole, 2-Bromo-4-nitroacetophenone and absolute Ethanol are added together and heated to reflux for approximately 24 hours. Tetrabutylammonium iodide is added and the reaction is refluxed an additional 12 hours. The resulting yellow suspension is cooled and the solids collected and washed with Ethanol and Diethyl ether. The solids are dried under vacuum to give Intermediate 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883783B2
Source datasetuspto-grants-2014_11
ORD IDord-996d97c419bc40769811793a3d83e76c
Source noteuspto-grants-2014_11