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1256821-98-3

1256821-98-3 Structure

1256821-98-3 Structure
IdentificationBack Directory
[Name]

6-Amino-5-methoxy-nicotinonitrile
[CAS]

1256821-98-3
[Synonyms]

6-Amino-5-methoxy-nicotinonitrile
3-Pyridinecarbonitrile, 6-amino-5-methoxy-
[Molecular Formula]

C7H7N3O
[MDL Number]

MFCD18261105
[MOL File]

1256821-98-3.mol
[Molecular Weight]

149.15
Chemical PropertiesBack Directory
[Boiling point ]

308.0±42.0 °C(Predicted)
[density ]

1.25±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

4.83±0.10(Predicted)
[Appearance]

Light yellow to yellow Solid
Spectrum DetailBack Directory
[Spectrum Detail]

6-Amino-5-methoxy-nicotinonitrile(1256821-98-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

ZINC CYANIDE

557-21-1

5-BROMO-3-METHOXYPYRIDIN-2-AMINE

42409-58-5

6-Amino-5-methoxy-nicotinonitrile

1256821-98-3

Under nitrogen protection, 5-bromo-3-methoxypyridin-2-amine (3.00 g, 14.8 mmol) was dissolved in N,N-dimethylformamide (55 mL), and zinc(II) cyanide (2.78 g, 23.6 mmol) and tetrakis(triphenylphosphine)palladium(0) (2.06 g, 1.77 mmol) were added sequentially. The reaction mixture was stirred at 100 °C for 4 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate and washed sequentially with saturated ammonium hydroxide solution and brine. The organic and aqueous phases were separated, and the organic phase was dried with anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent ratio: ethyl acetate/cyclohexane=1:5) to afford 6-amino-5-methoxypyridine-3-carbonitrile (1.2 g, 54% yield). The product characterization data were as follows: 1H NMR (400 MHz, CDCl3) δ 7.99 (s, 1H), 6.99 (s, 1H), 3.88 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 152.83, 144.58, 141.27, 118.32, 115.52, 97.66, 55.65; LC-MS (Method B): retention time 0.69 min, m/z 150 ([M+H]+).

[References]

[1] Patent: WO2013/37755, 2013, A1. Location in patent: Page/Page column 24
[2] Patent: EP2570404, 2013, A1. Location in patent: Paragraph 0075; 0076
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