N-bromobutanimide → HCID 178519375, compound

HRID 408541Notes

Reaction equation

HRID 408541 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([CH:10]=[O:11])=[CH:7][CH:8]=2)[CH:3]=[N:2]1.[Br:12]N1C(=O)CCC1=O>C(#N)C>[Br:12][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[C:6]([CH:10]=[O:11])[CH:5]=2)[NH:1][N:2]=1

Participants

4

Reactant 2

HCID 67184N-bromobutanimideHCID 212506441H-Indazole-5-carboxaldehyde

Product 1

HCID 178519375HCID 178519375, compoundYield 100.2%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

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.).

Workup

  1. temperatureunder reflux for 30 min
  2. concentrationconcentrated under reduced pressure
  3. dissolutionThe residue was dissolved in ethyl acetate (1500 ml)
  4. washthe solution was washed with water and with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe crude product was triturated with ethyl acetate
  9. filtrationAfter filtration
  10. customthe precipitate was dried under vacuum

Sources & evidence

ORD record
ord-b8b6c263bfa54189bdec42d7427ead77
Source dataset
uspto-grants-2014_06
Patent number
US08759341B2

Reaction notes

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