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6-PHENYL-PYRIDIN-2-YLAMINE

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6-PHENYL-PYRIDIN-2-YLAMINE Basic information

Product Name:
6-PHENYL-PYRIDIN-2-YLAMINE
Synonyms:
  • 2-AMINO-6-PHENYLPYRIDINE
  • AKOS 205-07
  • 6-Phenyl-2-pyridinaMine
  • 6-phenylpyridin-2-amine
  • Pyridine, 2-amino-6-phenyl-
  • 2-Pyridinamine, 6-phenyl-
  • 6-PHENYL-PYRIDIN-2-YLAMINE
  • 6-AMINO-2-PHENYLPYRIDINE
CAS:
39774-25-9
MF:
C11H10N2
MW:
170.21
Product Categories:
  • Amines
  • Aromatics
  • Heterocycle-Pyridine series
  • pharmacetical
Mol File:
39774-25-9.mol
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6-PHENYL-PYRIDIN-2-YLAMINE Chemical Properties

Melting point:
71-72℃
Boiling point:
348℃
Density 
1.133
Flash point:
191℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
5.93±0.10(Predicted)
Appearance
Off-white to yellow Solid
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Safety Information

Risk Statements 
41
Safety Statements 
26-39
HS Code 
2933399990
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6-PHENYL-PYRIDIN-2-YLAMINE Usage And Synthesis

Uses

A derivative of 2-aminopyridinium as potent antimalarial.

Synthesis

45644-21-1

98-80-6

39774-25-9

GENERAL STEPS: To a sealed tube was added a solution of anhydrous 1,4-dioxane (30 v/v) in 2-amino-6-chloropyridine (1.0 eq.), followed by phenylboronic acid (1.5 eq.) and finely ground potassium phosphate (2.0 eq.). The reaction mixture was degassed by nitrogen bubbling for 5 minutes, then palladium acetate (5 mol%) and di-tert-butylphosphinoferrocene (5 mol%) were added and degassing continued for 5 minutes. The reaction tube was sealed under nitrogen atmosphere and heated at 100 °C with vigorous stirring for 5 hours. Upon completion of the reaction, it was cooled to room temperature and the reaction mixture was vacuum filtered through a diatomaceous earth pad and the precipitate was washed with 1,4-dioxane. The filtrates were combined, concentrated under reduced pressure and purified by fast column chromatography (elution gradient: pure hexane to 1:1 hexane/ethyl acetate containing 2.5 vol% triethylamine) to give 6-phenylpyridin-2-amine.

References

[1] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 8, p. 2742 - 2750
[2] Tetrahedron Letters, 2005, vol. 46, # 20, p. 3573 - 3577
[3] New Journal of Chemistry, 2017, vol. 41, # 24, p. 15420 - 15432

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