HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 23152327, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 23152701 | HCID 23152701 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 23152327 | HCID 23152327 | 78% |
Reaction Steps
To a solution of ethyl 3-cyclohexyl-1-ethoxycarbonylmethyl-1H-pyrrolo[2,3-b]pyridine-6-carboxylate (463 mg, 1.34 mmol) in carbon tetrachloride (10 ml) was added N-bromosuccinimide (287 mg, 1.61 mmol), and the mixture was heated under reflux for 4 hr. The mixture was allowed to cool to room temperature and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate-5:1) to give ethyl 2-bromo-3-cyclohexyl-1-ethoxycarbonylmethyl-1H-pyrrolo[2,3-b]pyridine-6-carboxylate (457 mg, yield 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977331B1 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-09c5f4eafe33415ca42082ad841df6d4 |
| Source note | uspto-grants-2011_07 |