Hydrochloric Acid → 4-bromo-1H-indazole

HRID 1692735Notes

Reaction equation

HRID 1692735 reaction equation
[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[N:5][N:6]2C(=O)C.Cl>CO>[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[N:5][NH:6]2

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 454801851-Acetyl-4-bromo-1H-indazole

Product 1

HCID 223525484-bromo-1H-indazole

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of the 1-(4-bromo-indazol-1-yl)-ethanone A (3.09 g, 12.9 mmol) in MeOH (50 mL) was added 6N aqueous HCl (30 mL) and the mixture was stirred at room temperature for 7 h. The MeOH was evaporated and the mixture partitioned between EtOAc (2 50 mL) and water (50 mL). The combined organic layers were washed with brine (50 mL), separated and dried (MgSO4). The solvent was removed by evaporation under reduced pressure to give 4-bromo-1H-indazole B (2.36 g, 93%).

Workup

  1. customThe MeOH was evaporated
  2. customthe mixture partitioned between EtOAc (2 50 mL) and water (50 mL)
  3. washThe combined organic layers were washed with brine (50 mL)
  4. customseparated
  5. dry with materialdried (MgSO4)
  6. customThe solvent was removed by evaporation under reduced pressure

Sources & evidence

ORD record
ord-6e73e4956fec4a7e97c863e925b7c553
Source dataset
uspto-grants-2012_04
Patent number
US08158626B2

Reaction notes

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