HCID 23086769, compound → 1-(4-Aminophenyl)pyrazin-2(1H)-one

HRID 18539Notes

Reaction equation

HRID 18539 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[CH:15]=[CH:14][N:13]=[CH:12][C:11]2=[O:16])=[CH:6][CH:5]=1)([O-])=O>C(OCC)(=O)C.C(O)C>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([N:10]2[CH:15]=[CH:14][N:13]=[CH:12][C:11]2=[O:16])=[CH:8][CH:9]=1

Participants

4

Reactant 1

HCID 23086769HCID 23086769, compound

Product 1

HCID 230867681-(4-Aminophenyl)pyrazin-2(1H)-one

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 8857Ethyl AcetateSolvent

Procedure

To a solution of 520 mg 1-(4-Nitro-phenyl)-1H-pyrazin-2-one in 26 mL ethyl acetate and 1.3 mL ethanol, 2.7 g SnCl2 dihydrate were added and the reaction mixture was heated to reflux for 6 h. Then, after cooling to RT the mixture was stirred for 16 h. The precipitated product was collected by filtration and was pure enough for the next reaction step. Yield: 450 mg.

Workup

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux for 6 h
  3. filtrationThe precipitated product was collected by filtration
  4. customwas pure enough for the next reaction step

Sources & evidence

ORD record
ord-6aa73413b96e48a6a0c5bd166d0a548c
Source dataset
uspto-grants-2010_06
Patent number
US07741341B2

Reaction notes

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