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2-Amino-5-chloro-3-fluoropyridine

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2-Amino-5-chloro-3-fluoropyridine Basic information

Product Name:
2-Amino-5-chloro-3-fluoropyridine
Synonyms:
  • 2-Amino-5-chloro-3-fluoropyridine
  • 5-Chloro-3-fluoropyridin-2-amine
  • 2-Pyridinamine,5-chloro-3-fluoro-(9CI)
  • 2-Amino-5-chloro-3-fluoropyrid
  • 5-Chloro-3-fluoro-2-pyridinamine
  • 2-AMino-5-chloro-3-fluoropyridine
  • 2-Amino-5-chloro-3-fluoropyridine 97%
  • 2-Pyridinamine, 5-chloro-3-fluoro-
CAS:
246847-98-3
MF:
C5H4ClFN2
MW:
146.55
EINECS:
253-700-5
Product Categories:
  • Fluorine series
  • PYRIDINE
  • Amines
  • blocks
  • FluoroCompounds
  • Pyridines
  • Amines and Anilines
  • Heterocycles
Mol File:
246847-98-3.mol
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2-Amino-5-chloro-3-fluoropyridine Chemical Properties

Melting point:
91-95 °C
Boiling point:
195.9±35.0 °C(Predicted)
Density 
1.449±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
solid
pka
1.72±0.49(Predicted)
Appearance
White to light brown Solid
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Safety Information

Hazard Codes 
T,Xi
Risk Statements 
23/24/25-50
Safety Statements 
36/37-38-45-61-63
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
2
HazardClass 
IRRITANT
HS Code 
29333990
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2-Amino-5-chloro-3-fluoropyridine Usage And Synthesis

Synthesis

89402-43-7

246847-98-3

General procedure for the synthesis of 2-amino-3-fluoro-5-chloropyridine from 2,3-difluoro-5-chloropyridine: 5-chloro-2,3-difluoropyridine (100 g, 0.669 mol) and liquid ammonia (1.125 L, 8.025 mol) were placed in an autoclave. The kettle was sealed and the reaction was carried out at 120 °C for 24 hours. Upon completion of the reaction, the reaction mixture was cooled and formation of a yellowish solid precipitate was observed. The precipitate was separated by filtration and the filter cake was washed with deionized water. The filtrate was extracted with ethyl acetate, the organic layers were combined and dried with anhydrous sodium sulfate. Subsequently, the organic solvent was removed by distillation under reduced pressure, and a small amount of petroleum ether was added to the residue, which was filtered again to obtain a precipitate of the target compound 2-amino-3-fluoro-5-chloropyridine. The final product was obtained as 84.22 g in 85.94% yield.

References

[1] Patent: CN105669539, 2016, A. Location in patent: Paragraph 0058; 0059; 0060
[2] Patent: US2008/242695, 2008, A1. Location in patent: Page/Page column 34
[3] Patent: US2008/242695, 2008, A1. Location in patent: Page/Page column 34

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