Uses
5-Bromonicotinonitrile serves as a reagent in the synthesis of 5-[(1R,5S)-3,6-Diazabicyclo[3.2.0]heptan-6-yl]nicotinonitrile (A-366833, a novel nicotinic
acetylcholine receptor (nAChR) ligand), reacting with (1S,5S)-benzyl 3,6-diazabicyclo[3.2.0]heptane-3-carboxylate[2].
Synthesis
General procedure for the synthesis of 3-cyano-5-bromopyridine from 3,5-dibromopyridine: iPrMgCl (2M in THF, 4.1 mL) and THF (5 mL) were added to a flask containing dry LiCl (0.35 g, 8.24 mmol) at 15 °C. After stirring for 15 min, a solution of 3-bromo-1-benzylnitrile (1.46 g, 8.03 mmol) in THF (1 mL) was slowly added to the reaction mixture and stirring was continued for 15 min. Subsequently, DMF (1.3 mL, 12 mmol) was added dropwise at 0 °C and the mixture was stirred for 2 hours. Upon completion of the reaction, aqueous NH3 (7 mL, 28-30%) and I2 (4.06 g, 16 mmol) were added to the mixture. After stirring for 2 h at room temperature, the reaction mixture was poured into saturated aqueous Na2SO3 solution and extracted with CHCl3 (3 x 30 mL). The organic layers were combined, dried with Na2SO4 and filtered. After removing the solvent under reduced pressure, the residue was purified by silica gel short column chromatography (eluent: hexane/ethyl acetate = 9:1, v/v) to afford pure 3-cyano-5-bromopyridine (0.73 g) in 71% yield. Most of the nitrile compounds involved in this study were commercially available and were identified by comparison with real samples.
References
[1] Tetrahedron, 2013, vol. 69, # 5, p. 1462 - 1469
[2] Ji, J., Bunnelle, W. H., Anderson, D. J., Faltynek, C., Dyhring, T., Ahring, P. K., Rueter, L. E., Curzon, P., Buckley, M. J., Marsh, K. C., Kempf-Grote, A., & Meyer, M. D. (2007). A-366833: A novel nicotinonitrile-substituted 3,6-diazabicyclo[3.2.0]-heptane α4β2 nicotinic acetylcholine receptor selective agonist: Synthesis, analgesic efficacy and tolerability profile in animal models. Biochemical Pharmacology, 74(8), 1253–1262.
https://doi.org/10.1016/j.bcp.2007.08.010
