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4-amino-3,5-dichloro-6-fluoro-2-pyridone

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4-amino-3,5-dichloro-6-fluoro-2-pyridone Basic information

Product Name:
4-amino-3,5-dichloro-6-fluoro-2-pyridone
Synonyms:
  • 4-amino-3,5-dichloro-6-fluoro-2-pyridone
  • 4-AMINO-3,5-DICHLORO-6-FLUORO-2(1H)-PYRIDINONE
  • 4-amino-3,5-dichloro-6-difluoro-2(1H)-pyridinone
  • 4-Amino-3,5-dichloro-6-fluoropyridin-2(1H)-one
  • 4-Amino-3,5-dichloro-6-fluoropyridin-2-ol
  • 2-Hydroxy-3,5-dichloro-4-aMino-6-fluoropyridine
  • 4-Amino-3,5-dichloro-6-fluoro-1H-pyridin-2-one
  • Fluroxypyr pyridinol
CAS:
94133-62-7
MF:
C5H3Cl2FN2O
MW:
196.99
EINECS:
302-724-5
Mol File:
94133-62-7.mol
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4-amino-3,5-dichloro-6-fluoro-2-pyridone Chemical Properties

Boiling point:
134.7±40.0 °C(Predicted)
Density 
1.69±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
3.54±0.20(Predicted)
Appearance
White to off-white Solid
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4-amino-3,5-dichloro-6-fluoro-2-pyridone Usage And Synthesis

Synthesis

2840-00-8

94133-62-7

The general procedure for the synthesis of 6-fluoro-3,5-dichloro-4-amino-2-hydroxypyridine using 2,6-difluoro-3,5-dichloro-4-aminopyridine as starting material was as follows: accurately weighed 80 mmol of 2,6-difluoro-3,5-dichloro-4-amino-pyridine in a reaction flask, and 5,000 mL of N,N-dimethylacetamide (DMAC) was added to dissolve it completely. A 40 wt% aqueous sodium hydroxide solution was slowly added dropwise with continuous stirring. After the dropwise addition was completed, the reaction system was warmed up to 100 °C and the reaction was maintained at this temperature for 3 hours. After completion of the reaction, the mixture was cooled to room temperature and the target compound 6-fluoro-3,5-dichloro-4-amino-2-hydroxypyridine (Compound I) was isolated by suitable method in 94.5% yield.

References

[1] Patent: CN107311924, 2017, A. Location in patent: Paragraph 0060-0064; 0065-0069; 0070-0074

4-amino-3,5-dichloro-6-fluoro-2-pyridoneSupplier

Chiba Pharmaceutical Science and technology Co, Ltd.
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