Acetic Acid → HCID 19137005, compound

HRID 1756788Notes

Reaction equation

HRID 1756788 reaction equation
C(O)(=O)C.CC(O)C.[CH3:9][N:10]([CH3:23])[C:11]1[C:16]([N+:17]([O-])=O)=[C:15]([O:20][CH2:21][CH3:22])[N:14]=[CH:13][N:12]=1.C(=O)([O-])[O-].[K+].[K+]>O.[Fe].CC(C)=O>[NH2:17][C:16]1[C:11]([N:10]([CH3:9])[CH3:23])=[N:12][CH:13]=[N:14][C:15]=1[O:20][CH2:21][CH3:22]

Participants

8

Conditions

Temperature
80 °C

Procedure

A mixture of 3 g of iron dust, 0.3 g of acetic acid and 2.5 ml of water was refluxed with heating for 30 minutes, allowed to cool at 80° C. and mixed with 10 ml of 2-propanol and gradually 2.33 g of 4-dimethylamino-6-ethoxy-5-nitropyrimidine. The resultant mixture was stirred at the same temperature for 1 hour, allowed to cool at 40° C., mixed with solution of 0.9 g of potassium carbonate in 1.5 ml of water and stirred for further 1 hour. Acetone was added to the mixture, which was filtered through Celite. The filtrate was concentrated in vacuo, and the residue was mixed with water and shaken with ether. The organic layer was washed with water and saturated saline in order, dried over anhydrous sodium sulfate and the solvent evaporated to give 1.80 g of the titled compound.

Workup

  1. temperaturewas refluxed
  2. temperaturewith heating for 30 minutes
  3. temperatureto cool at 40° C.
  4. filtrationwas filtered through Celite
  5. concentrationThe filtrate was concentrated in vacuo
  6. additionthe residue was mixed with water
  7. stirringshaken with ether
  8. washThe organic layer was washed with water and saturated saline in order
  9. dry with materialdried over anhydrous sodium sulfate
  10. customthe solvent evaporated

Sources & evidence

ORD record
ord-af901d3a5c564a869eb08a30e01364b6
Source dataset
uspto-grants-1995_08
Patent number
US05442060

Reaction notes

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