HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzo(d)thiazol-2-amine → ethyl imidazo[2,1-b][1,3]benzothiazole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzo(d)thiazol-2-amine | HCID 8706 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl imidazo[2,1-b][1,3]benzothiazole-2-carboxylate | HCID 1480574 | — |
Reaction Steps
Ethyl bromopyruvate (9.8 g, 50 mmol) was added dropwise to a stirred solution of 2-aminobenzothiazole (7.5 g, 50 mmol) in DMF (100 ml) at room temperature. After the addition, the reaction mixture was heated to reflux for 6 h. The reaction mixture was cooled to room temperature and quenched with ice cold water. The aqueous layer was neutralized with NH4OH and the separated solid was filtered. It was washed well with water and dried. The crude product obtained was taken to next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691842B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-826f3b8e42574ee88dab8d45fe1c9626 |
| Source note | uspto-grants-2010_04 |