ChemicalBook--->CAS DataBase List--->98139-15-2

98139-15-2

98139-15-2 Structure

98139-15-2 Structure
IdentificationBack Directory
[Name]

4-AMINOPYRIDINE-2-CARBONITRILE
[CAS]

98139-15-2
[Synonyms]

4-AMINO-2-CYANOPYRIDINE
4-Aminopyridine-2-carbonitrile
2-Pyridinecarbonitrile, 4-amino-
2-Pyridinecarbonitrile,4-amino-(9CI)
4-AMINOPYRIDINE-2-CARBONITRILE ISO 9001:2015 REACH
[Molecular Formula]

C6H5N3
[MDL Number]

MFCD07374351
[MOL File]

98139-15-2.mol
[Molecular Weight]

119.12
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[RIDADR ]

UN2811
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

4-AMINOPYRIDINE-2-CARBONITRILE(98139-15-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

ZINC CYANIDE

557-21-1

4-Amino-2-chloropyridine

14432-12-3

4-aminopicolinonitrile

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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