2-Cyano-5-bromomethylpyridine
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
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
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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