HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 178519375, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1H-Indazole-5-carboxaldehyde | HCID 21250644 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178519375 | HCID 178519375 | 100.2% |
Reaction Steps
To a solution of 20 g (137 mmol) 1H-indazole-5-carbaldehyde in acetonitrile (580 ml), 28 g (157 mmol) 1-bromopyrrolidine-2,5-dione were added over 20 min at room temperature. The resulting suspension was stirred under reflux for 30 min, then cooled to room temperature and concentrated under reduced pressure. The residue was dissolved in ethyl acetate (1500 ml), and the solution was washed with water and with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was triturated with ethyl acetate. After filtration, the precipitate was dried under vacuum to yield the title compound as a white solid (30.9 g, 75% of th.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759341B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-b8b6c263bfa54189bdec42d7427ead77 |
| Source note | uspto-grants-2014_06 |