HCID 178418546, compound → 5-Nitro-1H-indazole-3-carbonitrile

HRID 1430935Notes

Reaction equation

HRID 1430935 reaction equation
I[C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[CH:9]=2)[NH:4][N:3]=1.[Cu][C:15]#[N:16]>CN1C(=O)CCC1.CCOC(C)=O>[N+:11]([C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[NH:4][N:3]=[C:2]2[C:15]#[N:16])([O-:13])=[O:12]

Participants

5

Reactant 2

HCID 178418546HCID 178418546, compoundHCID 178526495HCID 178526495, compound

Product 1

HCID 225672195-Nitro-1H-indazole-3-carbonitrileYield 20.3%

Reagents, catalysts & solvents 2

HCID 8857Ethyl AcetateSolventHCID 13387N-methyl-2-pyrrolidoneSolvent

Conditions

Temperature
160 °C

Procedure

3-iodo-5-nitro-1H-indazole (6.9 g, 23.87 mmol) was taken up in NMP (90 mL) and copper (I) cyanide (4.28 g, 47.7 mmol) was added. The reaction was heated at 160° C. for 1 h, then cooled to rt. The reaction mixture was diluted with EtOAc and filtered through celite, rinsing with EtOAc. The filtrate was washed 2× with water and 2× with brine. The organic layer was dried over Na2SO4, filtered, and concentrated. The crude material was purified by flash column chromatography eluting with 0%-50% EtOAc/Hex. 0.91 g of 5-nitro-1H-indazole-3-carbonitrile was obtained.

Workup

  1. temperaturecooled to rt
  2. filtrationfiltered through celite
  3. washrinsing with EtOAc
  4. washThe filtrate was washed 2× with water and 2× with brine
  5. dry with materialThe organic layer was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude material was purified by flash column chromatography
  9. washeluting with 0%-50% EtOAc/Hex

Sources & evidence

ORD record
ord-8bd21e51ddb74fa4a8a3b9f6a7321863
Source dataset
uspto-grants-2015_01
Patent number
US08940736B2

Reaction notes

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