HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 67148260, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 67147764 | HCID 67147764 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 67148260 | HCID 67148260 | — |
Reaction Steps
A mixture of methyl 3-(benzoyloxy)-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepine-2-carboxylate, N-bromo-succinimide (2 eq.) and α,α′-azoisobutyronitrile (0.45 eq.) in carbon tetrachloride was stirred under reflux for 14 hour. The mixture was cooled to room temperature, the succinimide was filtered off and the solvent was removed under reduced pressure. Methyl 3-(benzoyloxy)-10-bromo-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepine-2-carboxylate was obtained after flash chromatography (eluents petroleum ether/ethyl acetate, 8:2) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414045B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-8e25f124c51d45db97221a8361f9e441 |
| Source note | uspto-grants-2008_08 |