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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Dihydroxypyrimidine >  4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI)

4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI)

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4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI) Basic information

Product Name:
4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI)
Synonyms:
  • 5-fluoro-4-hydroxy-2-methyl-1H-pyrimidin-6-one
  • 5-Fluoro-6-hydroxy-2-methyl-4(1H)-pyrimidinone
  • 4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI)
  • 4(3H)-PyriMidinone,5-fluoro-6-hydroxy-2-Methyl-
  • 5-Fluoro-4,6-dihydroxy-2-methylpyrimidine
  • NSC 33038
  • 5-Fluoro-6-hydroxy-2-methylpyrimidin-4(3H)-one
  • 4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI) ISO 9001:2015 REACH
CAS:
1598-63-6
MF:
C5H5FN2O2
MW:
144.1
Product Categories:
  • PYRIMIDINE
Mol File:
1598-63-6.mol
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4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI) Chemical Properties

Melting point:
>310℃
Density 
1.59±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
4.19±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933599590
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4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI) Usage And Synthesis

Synthesis

344-14-9

124-42-5

1598-63-6

Part A: Synthesis of 5-fluoro-4,6-dihydroxy-2-methylpyrimidine. A methanolic solution of 25% sodium methanolate (0.84 mol) was diluted in 200 mL of methanol. To this solution, acetamidine hydrochloride (40 g, 0.42 mol) was added and white precipitate formation was observed. Subsequently, dimethyl fluoromalonate (70 g, 0.46 mol) was added. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the solvent was removed by vacuum concentration to give a dry residue. The residue was redissolved in 300 mL of hot water. After the aqueous solution was cooled to room temperature, concentrated hydrochloric acid was slowly added and the pH was adjusted to about 5. The formation of fine white prismatic crystals was observed. Concentrated hydrochloric acid was continued to be added dropwise to pH 3 and then the crystals were collected by filtration. The crystals were washed with 1 M hydrochloric acid and dried under vacuum to afford 5-fluoro-4,6-dihydroxy-2-methylpyrimidine (65.5 g, yield >100%).LCMS analysis showed (M + H)+: 145.

References

[1] Patent: WO2009/61879, 2009, A1. Location in patent: Page/Page column 60-61
[2] Patent: WO2013/82388, 2013, A1. Location in patent: Page/Page column 66-67

4(1H)-Pyrimidinone, 5-fluoro-6-hydroxy-2-methyl- (9CI)Supplier

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