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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038311Generated: October 26, 2026

Bicarbonate Ion → 2-(4-Nitrophenyl)imidazo[2,1-b]benzothiazol-7-ol

https://huagongshe.com/reaction/1038311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicarbonate IonHCID 769—
ReactantCarbonate IonHCID 19660—
Reactant2-Amino-6-benzothiazololHCID 33462—
Reactant2-Bromo-4'-nitroacetophenoneHCID 66840—
ReactantSodium BicarbonateHCID 516892—
Solvent1-ButanolHCID 263—
SolventEthanolHCID 702—
SolventIsopropanolHCID 3776—
Product2-(4-Nitrophenyl)imidazo[2,1-b]benzothiazol-7-olHCID 29933257—

Reaction Conditions

Temperature112.5 °C

Reaction Steps

Alternatively, the reaction may be carried out in the presence of a base, for example, in the presence of one or more carbonate or bicarbonate salt. For example, sodium bicarbonate is added to a mixture of 2-amino-6-hydroxybenzothiazole and 2-bromo-4-nitroacetophenone in a suitable solvent such as ethanol, isopropanol or n-butanol, and the resulting mixture is stirred at a suitable temperature, for example, to reflux and maintained at reflux (110-115° C.) for 2-3 h or until the reaction is substantially complete.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551963B2
Source datasetuspto-grants-2013_10
ORD IDord-0f8120178e0f487cad158d5a5ce7024f
Source noteuspto-grants-2013_10