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4-aminopicolinonitrile

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4-aminopicolinonitrile Basic information

Product Name:
4-aminopicolinonitrile
Synonyms:
  • 2-Pyridinecarbonitrile,4-amino-(9CI)
  • 4-AMINO-2-CYANOPYRIDINE
  • 4-Aminopyridine-2-carbonitrile
  • 2-Pyridinecarbonitrile, 4-amino-
  • 4-AMINOPYRIDINE-2-CARBONITRILE ISO 9001:2015 REACH
  • 4-AMINOPICOLINONITRILE
CAS:
98139-15-2
MF:
C6H5N3
MW:
119.12
Product Categories:
  • Pyridine series
  • Pyridines
  • PYRIDINE
Mol File:
98139-15-2.mol
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4-aminopicolinonitrile Chemical Properties

Melting point:
145 °C
Boiling point:
368.2±22.0 °C(Predicted)
Density 
1.23±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
3.87±0.30(Predicted)
Appearance
Off-white to brown Solid
InChI
InChI=1S/C6H5N3/c7-4-6-3-5(8)1-2-9-6/h1-3H,(H2,8,9)
InChIKey
GMKRESMCPMIWGU-UHFFFAOYSA-N
SMILES
C1(C#N)=NC=CC(N)=C1
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Safety Information

RIDADR 
UN2811
HS Code 
2933399990
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4-aminopicolinonitrile Usage And Synthesis

Synthesis

557-21-1

14432-12-3

98139-15-2

2-Chloro-4-aminopyridine (0.642 g, 5 mmol), zinc cyanide (0.323 g, 2.75 mmol) and tetrakis(triphenylphosphine)palladium (0.288 g, 0.025 mmol) were mixed in 5 mL N,N-dimethylformamide (DMF). The reaction mixture was heated at 145°C for 20 hours. After completion of the reaction, it was cooled to room temperature and subsequently partitioned between ethyl acetate and water. The aqueous layer was extracted with additional ethyl acetate. The organic layers were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by fast column chromatography on silica gel, using 9:1 hexane/ethyl acetate as eluent to give 0.29 g (20% yield) of 4-aminopyridine-2-carbonitrile. Mass spectrum (DCI) m/e 120 (M + H)+; 1H NMR (300 MHz, DMSO-D6) δ 8.08 (d, J = 5.76 Hz, 1H), 6.94 (d, J = 2.34 Hz, 1H), 6.68 (dd, J = 5.76,2.37 Hz, 1H), 6.59 (s, 2H).

References

[1] Patent: WO2004/76424, 2004, A1. Location in patent: Page 131

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