Urea → HCID 20295827, compound

HRID 1366382Notes

Reaction equation

HRID 1366382 reaction equation
[NH2:1][C:2]([NH2:4])=[O:3].[F:5][CH:6]([C:11](OC)=[O:12])[C:7](OC)=[O:8].C[O-].[Na+]>CO>[F:5][C:6]1[C:7](=[O:8])[NH:1][C:2](=[O:3])[NH:4][C:11]=1[OH:12]

Participants

5

Procedure

A mechanically stirred solution of urea (60.06 g, 1 mol) and dimethyl fluoromalonate (150.11 g, 1 mol) in methanol (1 L) was treated with 25 wt % NaOMe in methanol (˜4.6 M, 435 mL, 2 mol). The mixture was refluxed for 3 h and then allowed to cool to room temperature. The mixture was filtered, the wet cake was dissolved in warm water (˜1.2 L), and the resulting aqueous solution was acidified with concentrated aqueous HCl (˜160 mL) to pH=2 while stirring over 1 h. The mixture was allowed to cool to room temperature, and the product was filtered and washed thoroughly with water, then dried under vacuum to give 5-fluoro-6-hydroxy-2,4(1H,3H)-pyrimidinedione (80 g, 55%) as a white solid. LCMS: (M+H)+: 147.0.

Workup

  1. temperatureThe mixture was refluxed for 3 h
  2. filtrationThe mixture was filtered
  3. dissolutionthe wet cake was dissolved in warm water (˜1.2 L)
  4. temperatureto cool to room temperature
  5. filtrationthe product was filtered
  6. washwashed thoroughly with water
  7. customdried under vacuum

Sources & evidence

ORD record
ord-242e447d5010459a844501613bf645e7
Source dataset
uspto-grants-2011_02
Patent number
US07893056B2

Reaction notes

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