Glyoxal → HCID 178517228, compound

HRID 1031108Notes

Reaction equation

HRID 1031108 reaction equation
[NH2:1][C:2]1[C:11]([NH2:12])=[C:10]([Cl:13])[CH:9]=[C:8]2[C:3]=1[N:4]=[C:5]([OH:15])[C:6]([OH:14])=[N:7]2.[CH:16]([CH:18]=O)=O.C(=O)([O-])[O-].[Na+].[Na+]>O>[Cl:13][C:10]1[CH:9]=[C:8]2[N:7]=[C:6]([OH:14])[C:5]([OH:15])=[N:4][C:3]2=[C:2]2[C:11]=1[N:12]=[CH:18][CH:16]=[N:1]2

Participants

5

Reactant 3

HCID 7860GlyoxalHCID 10340Sodium CarbonateHCID 178507817HCID 178507817, compound

Product 1

HCID 178517228HCID 178517228, compoundYield 100.6%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
50 °C

Procedure

A mixture of 0,5 g (2,24 mmol) 5,6-diamino-7-chloro-2,3-dihydroxyquinoxaline in 20 ml water was added 0,5 ml (3,36 mmol) 40% aqueous glyoxal and 0,35 g (3,36 mmol) sodium carbonate. The reaction mixture was stirred at 50° C. for 3 h. After cooling to 25° C., the precipitate was filtered off. The crude product was stirred with water and added 1N hydrochloric acid to pH 2-3 to give 0,56 g (100%) 6-chloro-2,3-dihydroxypyrazino(2,3-f)quinoxaline, m.p. >300° C. NMR (DMSO-d6): 9.0 (2H,s), 7.73 (1H,s).

Workup

  1. temperatureAfter cooling to 25° C.
  2. filtrationthe precipitate was filtered off
  3. stirringThe crude product was stirred with water
  4. additionadded 1N hydrochloric acid to pH 2-3

Sources & evidence

ORD record
ord-da2cc388ce674539a16f8c7aa1c84d14
Source dataset
uspto-grants-1992_04
Patent number
US05109001

Reaction notes

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