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5-chloro-4-nitro-1H-indazole → 5-Chloro-1H-indazol-4-amine

HRID 1869402
Notes
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Reaction equation

HRID 1869402 reaction equation
[Cl:1][C:2]1[C:3]([N+:11]([O-])=O)=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][N:6]=[CH:5]2>[Pd]>[Cl:1][C:2]1[C:3]([NH2:11])=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][N:6]=[CH:5]2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 179892685-chloro-4-nitro-1H-indazole

Product 1

HCID 179892615-Chloro-1H-indazol-4-amine

Reagents, catalysts & solvents 1

HCID 23938PalladiumCatalyst

Procedure

A solution that consists of 5-chloro-4-nitro-1H-indazole (872 mg, 4.41 mmol) is mixed with 150 mg of palladium on carbon (10%) and stirred under hydrogen atmosphere at room temperature. After 45 minutes, the catalyst is suctioned off on one frit and washed with methanol. The filtrate is concentrated by evaporation, and the residue is taken up in 200 ml of ethyl acetate and heated. After renewed suctioning-off and concentration by evaporation of the filtrate, the purification on silica gel is carried out with hexane/ethyl acetate (100-33% hexane). 296 mg (40% of theory) of the product is obtained.

Workup

  1. washwashed with methanol
  2. concentration
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
The filtrate is concentrated by evaporation
  • temperatureheated
  • concentrationconcentration
  • customby evaporation of the filtrate
  • customthe purification on silica gel
  • custom296 mg (40% of theory) of the product is obtained
  • Sources & evidence

    ORD record
    ord-8ec87901cb0c4796b9a0c1d7c65f51b7
    Source dataset
    uspto-grants-2009_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07638515B2

    Reaction notes

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