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4-(PHENYLAMINO)PYRIDINE

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4-(PHENYLAMINO)PYRIDINE Basic information

Product Name:
4-(PHENYLAMINO)PYRIDINE
Synonyms:
  • N-(4-Pyridyl)aniline
  • 4-ANILINOPYRIDINE
  • 4-PYRIDINAMINE, N-PHENYL-
  • 4-(PHENYLAMINO)PYRIDINE
  • AKOS BC-0724
  • N-phenylpyridin-4-amine
  • phenyl-(4-pyridyl)amine
  • N-phenyl-4-pyridinamine
CAS:
22961-45-1
MF:
C11H10N2
MW:
170.21
EINECS:
245-352-8
Product Categories:
  • Pyridines, Pyrimidines, Purines and Pteredines
Mol File:
22961-45-1.mol
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4-(PHENYLAMINO)PYRIDINE Chemical Properties

Melting point:
177 °C
Boiling point:
324.0±15.0 °C(Predicted)
Density 
1.144±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
soluble in Methanol
form 
powder to crystalline
pka
6.90±0.10(Predicted)
color 
White to Orange to Green
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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4-(PHENYLAMINO)PYRIDINE Usage And Synthesis

Synthesis

1120-87-2

62-53-3

22961-45-1

The general procedure for the synthesis of N-phenylpyridin-4-amine from 4-bromopyridine and aniline was as follows: 3.16 g (20.0 mmol) of 4-bromopyridine, 2.79 g (30.0 mmol) of aniline, 0.37 g (0.4 mmol) of Pd2(dba)3, 0.08 g (0.4 mmol) of PtBu3 and 2.88 g (30.0 mmol ) KOtBu were dissolved in 60 mL of toluene to form a homogeneous solution. Subsequently, the reaction mixture was stirred at 85 °C for 4 hours. After completion of the reaction, the reaction solution was cooled to room temperature and extracted three times with 50 mL of water and 50 mL of diethyl ether. The organic phases were combined, dried with magnesium sulfate, and then the solvent was removed by rotary evaporation. Finally, the residue was separated and purified using silica gel column chromatography to afford 1.49 g of intermediate I-3 in 88% yield. The resulting compound was characterized by LC-MS.

References

[1] Patent: CN102850322, 2016, B. Location in patent: Paragraph 0150-0153
[2] Patent: CN108822041, 2018, A. Location in patent: Paragraph 0073; 0074; 0078

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