6-nitro-1H-indole-2-carbonitrile → 6-Amino-1H-indole-2-carbonitrile

HRID 1847455Notes

Reaction equation

HRID 1847455 reaction equation
[N+:1]([C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]#[N:14])[NH:10]2)=[CH:6][CH:5]=1)([O-])=O>[Ni].CCO>[NH2:1][C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]#[N:14])[NH:10]2)=[CH:6][CH:5]=1

Participants

4

Reactant 1

HCID 574701946-nitro-1H-indole-2-carbonitrile

Product 1

HCID 451170156-Amino-1H-indole-2-carbonitrileYield 49%

Reagents, catalysts & solvents 2

HCID 935NickelCatalystHCID 702EthanolSolvent

Procedure

A mixture of 6-nitro-1H-indole-2-carbonitrile (2.5 g, 13 mmol) and Raney Nickel (500 mg) in EtOH (50 mL) was stirred at room temperature under H2 (1 atm) for 1 h. Raney, Nickel was removed via filtration and the filtrate was evaporated under reduced pressure to give a residue, which was purified by column chromatography on silica get to give 6-amino-1H-indole-2-carbonitrile (1.0 g, 49%). 1H NMR (DMSO-d6) δ 12.75 (br s, 1H), 7.82 (d, J=8 Hz, 1H), 7.57 (s, 1H), 7.42 (s, 1H), 7.15 (d, J=8 Hz, 1H); MS (ESI) m/e (M+H+) 158.2.

Workup

  1. customRaney, Nickel was removed via filtration
  2. customthe filtrate was evaporated under reduced pressure
  3. customto give a residue, which
  4. customwas purified by column chromatography on silica
  5. customget

Sources & evidence

ORD record
ord-ee4b7323e69e4ad3ac5a143c5343c3dc
Source dataset
uspto-grants-2015_02
Patent number
US08952050B2

Reaction notes

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