HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-6-benzothiazolol → 2-(4-Nitrophenyl)imidazo[2,1-b]benzothiazol-7-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-6-benzothiazolol | HCID 33462 | — |
| Reactant | 2-Bromo-4'-nitroacetophenone | HCID 66840 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Nitrophenyl)imidazo[2,1-b]benzothiazol-7-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883783B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-996d97c419bc40769811793a3d83e76c |
| Source note | uspto-grants-2014_11 |