HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → [2-[(5-Bromo-3-carbamoyl-2-thienyl)amino]-1,1-dimethyl-2-oxo-ethyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | [2-[(3-Carbamoyl-2-thienyl)amino]-1,1-dimethyl-2-oxo-ethyl]acetate | HCID 117717784 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | [2-[(5-Bromo-3-carbamoyl-2-thienyl)amino]-1,1-dimethyl-2-oxo-ethyl]acetate | HCID 117717729 | — |
Reaction Steps
Intermediate 10 (46.5 g, 172 mmol) is dissolved in AcOH (700 mL). To the resulting suspension, NBS (32.2 g, 181 mmol) is added. The mixture is stirred at room temperature, after which it is evaporated to give a slurry. This slurry is taken up in water to give a suspension that is filtered. Resulting precipitate is dried in the vacuum oven and used as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09382254B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-be3a8bf432934a80b6093a77f65b2733 |
| Source note | uspto-grants-2016_07 |