How to cite this paper
Khandebharad, A., Sarda, S., Soni, M., Gill, C., Kulkarni, P & Agrawal, B. (2018). NaCl: a facile, environmentally benign catalyst for the synthesis of pyrazole 4-carbonitrile in aqueous media.Current Chemistry Letters, 7(2), 57-64.
Refrences
1. Bye J. W., and Falconer R. J. (2015) A study of the relationship between water and anions of the Hofmeister series using pressure perturbation calorimetry. Phys Chem Chem Phys, 17 (21) 14130–14137.
2. Dandia A., Gupta S. L., and Parewa V. (2014) An efficient ultrasound-assisted one-pot chemoselective synthesis of pyrazolo[3,4-b] pyridine-5-carbonitriles in aqueous medium using NaCl as a catalyst. RSC Adv, 4 (14) 6908-6915.
3. Gujar J. B., Chaudhari M. A., Kawade D. S., and Shingare M. S. (2014) Sodium chloride: A proficient additive for the synthesis of pyridine derivatives in aqueous medium. Tetrahedron Lett, 55 (50) 6939–6942.
4. Chanda A., and Fokin V. V. (2009) Organic synthesis “on water.” Chem Rev, 109 (2) 725-748.
5. Tisseh Z. N., Dabiri M., Nobahar M., Khavasi H. R., and Bazgir A. (2012) Catalyst-free, aqueous and highly diastereoselective synthesis of new 5-substituted 1H-tetrazoles via a multi-component domino Knoevenagel condensation/1,3 dipolar cycloaddition reaction. Tetrahedron, 68 (6) 1769–1773.
6. Balbi A., Anzaldi M., MacCi C., Aiello C., Mazzei M., Gangemi R., and Viale M. (2011) Synthesis and biological evaluation of novel pyrazole derivatives with anticancer activity. Eur J Med Chem, 46 (11) 5293–5309.
7. El-Sayed M. A.-A., Abdel-Aziz N. I., Abdel-Aziz A. A.-M., El-Azab A. S., Asiri Y. A., and ElTahir K. E. H. (2011) Design, synthesis, and biological evaluation of substituted hydrazone and pyrazole derivatives as selective COX-2 inhibitors: Molecular docking study. Bioorg. Med. Chem., 19 (11) 3416–3424.
8. Bandgar B. P., Chavan H. V., Adsul L. K., Thakare V. N., Shringare S. N., Shaikh R. and Gacche R. N. (2013) Design, synthesis, characterization and biological evaluation of novel pyrazole integrated benzophenones. Bio Med Chem Lett, 23 (3) 912–916.
9. Szabó G., Fischer J., Kis-Varga Á. and Gyires K. (2008) New celecoxib derivatives as anti-inflammatory agents. J Med Chem, 51 (1) 142–147.
10. Tanitame A., Oyamada Y., Ofuji K., Terauchi H., Kawasaki M., Wachi M., and Yamagishi J. (2005) Synthesis and antibacterial activity of a novel series of DNA gyrase inhibitors: 5-[(E)-2-arylvinyl]pyrazoles. Bio Med Chem Lett, 15 (19) 4299–4303.
11. Dias L. R. S., and Salvador R. R. S. (2012) Pyrazole carbohydrazide derivatives of pharmaceutical interest. Pharmaceuticals, 5 (3) 317–324.
12. Ismail N. S. M., Ali G. M. E., Ibrahim D. A., and Elmetwali A. M. (2016) Medicinal attributes of pyrazolo[1,5-a]pyrimidine based scaffold derivatives targeting kinases as anticancer agents. Future J Pharm Sci, 2 (2) 60–70.
13. Genin M. J., Biles C., Keiser B. J., Poppe S. M., Swaney S. M., Tarpley W. G. and Romero, D. L. (2000). Novel 1,5-diphenylpyrazole nonnucleoside HIV-1 reverse transcriptase inhibitors with enhanced activity versus the delavirdine-resistant P236L mutant: Lead identification and SAR of 3- and 4-substituted derivatives. J Med Chem, 43 (5) 1034–1040.
14. Momose Y., Maekawa T., and Odaka H, K. H. (2001) 5-membered n-heterocyclic compounds with hypoglycemic and hypolipidemic activity.US patent 7179823
15. Penning T. D., Talley J. J., Bertenshaw S. R., Carter J. S., Collins P. W., Docter, S.,and Isakson P. C. (1997) Synthesis and biological evaluation of the 1,5-diarylpyrazole class of cyclooxygenase-2 inhibitors: identification of 4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benze nesulfonamide (SC-58635, celecoxib). J Med Chem, 40 (9) 1347–1365.
16. Abadi A. H., Eissa A. A. H., and Hassan G. S. (2003) Synthesis of novel 1,3,4-trisubstituted pyrazole derivatives and their evaluation as antitumor and antiangiogenic agents. Chem Pharm Bulletin, 51 (7) 838–44.
17. Kumari S., Shekhar A. and Pathak D. D. (2016) Graphene oxide-TiO2 composite: An efficient heterogeneous catalyst for the green synthesis of pyrazoles and pyridines. New J Chem, 40 (6) 5053-5060.
18. Srivastava M., Rai P., Singh J. and Singh J. (2014) Efficient iodine-catalyzed one pot synthesis of highly functionalised pyrazoles in water. New J Chem, 38 (1) 302–307.
19. Srivastava M., Rai P., Singh J., and Singh J. (2013) An environmentally friendlier approach—ionic liquid catalysed, water promoted and grinding induced synthesis of highly functionalised pyrazole derivatives. RSC Adv, 3 (38) 16994-16998.
20. Zolfigol M. A., Afsharnadery F., Baghery S., Salehzadeh S., and Maleki F. (2015) Catalytic applications of {[HMIM]C(NO2)3}: as a nano ionic liquid for the synthesis of pyrazole derivatives under green conditions and a mechanistic investigation with a new approach. RSC Adv, 5 (92) 75555–75568.
21. Esfandiary N., Nakisa A., Azizi K., Azarnia J., Radfar I., and Heydari A. (2017) Glucose-coated superparamagnetic nanoparticle-catalysed pyrazole synthesis in water. App Org Chemistry, 31 (7) https://doi.org/10.1002/aoc.3641
22. Rakhtshah J., Salehzadeh S., Godwini E., Maleki F., Baghery S., and Zolfigol M. A. (2016) Synthesis of pyrazole derivatives in the presence of a dioxomolybdenum complex supported on silica-coated magnetite nanoparticles as an efficient and easily recyclable catalyst. RSC Adv, 6 (106) 104875–104885.
23. Maddila S., Rana S., Pagadala R., Kankala S., Maddila S. and Jonnalagadda S. B. (2015) Synthesis of pyrazole-4-carbonitrile derivatives in aqueous media with CuO/ZrO2 as recyclable catalyst. Cat Comm, 61 26–30.
24. Yadav S., Rai P., Srivastava M., Singh J., Tiwari K. P., and Singh J. (2015) Atmospheric oxygen mediated synthesis of pyrazole under visible irradiation. Tetrahedron Lett, 56 (43) 5831–5835.
25. Hasaninejad A. and Firoozi S. (2013) Catalyst-free, one-pot, three-component synthesis of 5-amino-1,3-aryl-1- pyrazole-4-carbonitriles in green media. Mol Diversity, 17 (3) 459–469.
26. Nemati F., Nikkhah S. H. and Elhampour A. (2015) An environmental friendly approach for the catalyst-free synthesis of highly substituted pyrazoles promoted by ultrasonic radiation. Chin Chem Lett, 26 (11) 1397–1399.
27. Corradi A., Leonelli C., Rizzuti A., Rosa R., Veronesi P., Grandi R., Baldasari S., and Villa C. (2007) New “Green” Approaches to the Synthesis of Pyrazole Derivatives.Moleecule, 12 (7) 1482–1495.
28. Bhale P. S., Dongare S. B. and Chanshetti U. B. (2014) Simple Grinding, Catalyst-free, One-Pot, Three-Component Synthesis of Polysubstituted Amino Pyrazole. Res J Chem Sci, 4 (9) 2231–606.
29. Sarda S. R., Kale J. D., Wasmatkar S. K., Kadam V. S., Ingole P. G., Jadhav W. N. and Pawar R. P. (2009) An efficient protocol for the synthesis of 2-amino-4,6-diphenylpyridine-3-carbonitrile using ionic liquid ethylammonium nitrate. Mol Diversity, 13 (4) 545–549.
30. Bowen W. R. and Yousef H. N. S. (2003) Effect of salts on water viscosity in narrow membrane pores. J Coll Int Sci, 264 (2) 452–457.
31. Endo S., Pfennigsdorff A., and Goss K. U. (2012) Salting-out effect in aqueous NaCl solutions: Trends with size and polarity of solute molecules. Environ Sci Technol, 46 (3) 1496–1503.
32. Hasseine A., Meniai A. H., and Korichi, M. (2009) Salting-out effect of single salts NaCl and KCl on the LLE of the systems (water + toluene + acetone), (water + cyclohexane + 2-propanol) and (water + xylene + methanol). Desalination, 242 (1–3), 264–276.