Glyoxal → Lcb-2183

HRID 1681049Notes

Reaction equation

HRID 1681049 reaction equation
S(S([O-])=O)([O-])=O.[Na+].[Na+].[NH2:9][C:10]1[N:15]=[C:14]([CH2:16][O:17][CH2:18][CH3:19])[NH:13][C:12](=[O:20])[C:11]=1[N:21]=O.[CH:23]([CH:25]=O)=O>O>[CH2:18]([O:17][CH2:16][C:14]1[NH:13][C:12](=[O:20])[C:11]2[C:10](=[N:9][CH:23]=[CH:25][N:21]=2)[N:15]=1)[CH3:19]

Participants

5

Procedure

A solution of 19.1 g (0.11 mole) of sodium dithionite in 88 ml of water is added dropwise to a suspension, maintained at 20° C., of 10.0 g (0.050 mole) of 6-amino-2-(ethoxymethyl)-5-nitroso-4(3H)-pyrimidinone in 50 ml of water. After being stirred for 30 minutes at room temperature, the reaction mixture, still maintained at 20° C., is treated with 47.9 g (0.33 mole) of a 40% aqueous solution of glyoxal. Stirring is continued for 20 hours at room temperature. The solution obtained is then extracted with dichloromethane. These organic extracts are dried over sodium sulphate and concentrated to dryness under reduced pressure. The solid residue is recrystallized from methanol in the presence of Norit. Yld: 6.5 g (63%), m.p. 168°-169° C. The product is identical to that obtained in Example 1.

Workup

  1. temperaturethe reaction mixture, still maintained at 20° C.
  2. stirringStirring
  3. waitis continued for 20 hours at room temperature
  4. customThe solution obtained
  5. extractionis then extracted with dichloromethane
  6. dry with materialThese organic extracts are dried over sodium sulphate
  7. concentrationconcentrated to dryness under reduced pressure
  8. customThe solid residue is recrystallized from methanol in the presence of Norit
  9. customthat obtained in Example 1

Sources & evidence

ORD record
ord-035e51675bb04319929f044616797ab6
Source dataset
uspto-grants-1992_12
Patent number
US05167949

Reaction notes

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