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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | 2-Amino-6-benzothiazolol | HCID 33462 | — |
| Reactant | 2-Bromo-4'-nitroacetophenone | HCID 66840 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-(4-Nitrophenyl)imidazo[2,1-b]benzothiazol-7-ol | HCID 29933257 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08551963B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-0f8120178e0f487cad158d5a5ce7024f |
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| Source note | uspto-grants-2013_10 |
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