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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Methylpyrimidine >  4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINE

4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINE

Basic information Safety Supplier Related

4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINE Basic information

Product Name:
4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINE
Synonyms:
  • 4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINE
  • 2-Methyl-4,6-dichloro-5-fluoropyrimidine
  • PyriMidine, 4,6-dichloro-5-fluoro-2-Methyl-
  • 4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINE ISO 9001:2015 REACH
CAS:
105806-13-1
MF:
C5H3Cl2FN2
MW:
181
Product Categories:
  • Fluorine series
Mol File:
105806-13-1.mol
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4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINE Chemical Properties

Boiling point:
221℃
Density 
1.504
Flash point:
87℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-4.96±0.39(Predicted)
Appearance
Off-white to light green Solid
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933599590
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4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINE Usage And Synthesis

Synthesis

1598-63-6

105806-13-1

Part B: Synthesis of 4,6-dichloro-5-fluoro-2-methylpyrimidine. 5-Fluoro-4,6-dihydroxy-2-methylpyrimidine (60 g, 0.42 mol) was dissolved in 300 mL of phosphorus oxychloride (POCl3) and reacted at 120 °C for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated under reduced pressure until the rate of evaporation of the solvent decreased to less than 1 drop/sec. Care was taken to avoid over-concentration to prevent loss of product due to volatilization. The concentrated crude product was slowly poured into crushed ice and the slurry was stirred for 1 hour and allowed to warm naturally to room temperature. The precipitated yellow solid was collected by filtration, washed with cold water and briefly air dried to a flow-through state. Finally, the solid was thoroughly dried in a desiccator filled with phosphorus pentoxide (P2O5) to give pure 4,6-dichloro-5-fluoro-2-methylpyrimidine (59 g, 79% yield). LCMS analysis showed (M + H)+ peaks located at 181/183.

References

[1] Patent: WO2009/61879, 2009, A1. Location in patent: Page/Page column 61
[2] Patent: WO2013/82388, 2013, A1. Location in patent: Page/Page column 67
[3] Patent: WO2007/75852, 2007, A2. Location in patent: Page/Page column 32
[4] Patent: US2007/197523, 2007, A1. Location in patent: Page/Page column 7
[5] Patent: US4617393, 1986, A

4,6-DICHLORO-5-FLUORO-2-METHYLPYRIMIDINESupplier

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