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2-Cyano-5-bromomethylpyridine

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2-Cyano-5-bromomethylpyridine Basic information

Product Name:
2-Cyano-5-bromomethylpyridine
Synonyms:
  • 5-(BROMOMETHYL)PYRIDINE-2-CARBONITRILE
  • 5-(Bromomethyl)-2-cyanopyridine, 5-(Bromomethyl)picolinonitrile
  • 2-cyano-5-broMide-Methyl pyridine
  • 5-(broMoMethyl)-2-pyridinecarbonitrile
  • 2-Pyridinecarbonitrile, 5-(broMoMethyl)-
  • 2-Cyano-5-bromomethylpyridine
  • 5-(bromomethyl)picolinonitrile
  • 2-Cyano-5-bromomethylpyridine ISO 9001:2015 REACH
CAS:
308846-06-2
MF:
C7H5BrN2
MW:
197.03
Product Categories:
  • Methyl Halides
  • Methyl Halides
  • Pyridines
Mol File:
308846-06-2.mol
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2-Cyano-5-bromomethylpyridine Chemical Properties

Boiling point:
329.5±32.0 °C(Predicted)
Density 
1.60±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-1.23±0.10(Predicted)
Appearance
Light brown to brown Solid
InChI
InChI=1S/C7H5BrN2/c8-3-6-1-2-7(4-9)10-5-6/h1-2,5H,3H2
InChIKey
VEPVNICICSNYPW-UHFFFAOYSA-N
SMILES
C1(C#N)=NC=C(CBr)C=C1
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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2-Cyano-5-bromomethylpyridine Usage And Synthesis

Synthesis

1620-77-5

308846-06-2

General procedure for the synthesis of 5-(bromomethyl)-2-cyanopyridine using 2-cyano-5-methylpyridine as starting material: commercially available 2-cyano-5-methylpyridine (1.90 g, 16.1 mmol) was dissolved in chloroform (100 mL), followed by the addition of N-bromosuccinimide (4.29 g, 24.1 mmol) and α,α-azobisisobutyronitrile (0.792 g, 4.82 mmol). The reaction mixture was stirred at 60 °C for 6 hours. After completion of the reaction, the mixture was cooled in an ice bath, the precipitate was separated by filtration and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to afford the target compound 5-(bromomethyl)-2-cyanopyridine (1.69 g, 53% yield).1H NMR (CDCl3) δ (ppm): 4.80 (s, 2H), 8.03 (dd, J = 0.92, 8.07 Hz, 1H), 8.12 (dd, J = 2.20, 8.07 Hz. 1H), 8.81 (d, J = 1.83 Hz, 1H).

References

[1] Patent: EP2163554, 2010, A1. Location in patent: Page/Page column 52-53
[2] Patent: WO2007/28083, 2007, A2. Location in patent: Page/Page column 69-70
[3] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 7, p. 1017 - 1022
[4] Journal of Medicinal Chemistry, 2003, vol. 46, # 17, p. 3612 - 3622
[5] Patent: WO2011/20615, 2011, A1. Location in patent: Page/Page column 57; 58

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