How to cite this paper
Khalafy, J., Farajzadeh, S., Marjani, A & Asl, H. (2014). Single crystal X-ray structure of 3-amino-5-(4-chlorophenyl)pyridazine-4-carbonitrile.Current Chemistry Letters, 3(1), 1-6.
Refrences
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2. Rohet F., Rubat C., Coudert P., and Couquelet J. (1997) Synthesis and analgesic effects of 3-substituted 4,6-diarylpyridazine derivatives of the arylpiperazine class. Bioorg. Med. Chem., 5, 655-659.
3. Deeb A., Mourad E., and Elenany D. (2009) Pyridazine Derivatives and Related Compounds, Part 221: Synthesis, Reactions, and Insecticidal Activity of 3-Amino-5,6-diaryl-1H-pyrazolo[3,4-c]pyridazines. Phosphorus, Sulfur, and Silicon and the Related Elements., 185, 222-231.
4. Foks H., Wisterowicz K., Miszke A., Brozewicz K., Wisniewska K., and Dabrowska-Szponar M. (2009) Synthesis, Fungicidal and Antibacterial Activity of New Pyridazine Derivatives. Heterocycles., 78, 961-976.
5. Lamberth C., Trah S., Wendeborn S., Dumeunier R., Courbot M., Godwin J., and Schneiter P. (2012) Synthesis and fungicidal activity of tubulin polymerisation promoters. Part 2: Pyridazines. Bioorg. Med. Chem., 20, 2803–2810.
6. Smolyar N. N., Yutilov Yu. M., and Gres?ko, S. V. (2009) Synthesis of 4-amino-6-(hetaryl)pyridazin-3-ones as analogs of pyridazine-based cardiotonic agents. Pharm. Chem. J., 43, 87-88.
7. Ungureanu M., Mangalagiu I., Grosu G., and Petrovanu M. (1997) Antimicrobial activity of new pyridazine derivatives. Ann. Pharm. Fr., 55, 69-72.
8. Amer A. M., El-Mobayed M., Ateya A. M., and Muhdi T. S. (2002) On Condensation Reactions of Aceanthrene Quinone: Novel Heterocycles. Monatsh. Chem., 133, 79-88.
9. Gomaa M. Abdel-Motaal. (2003) An efficient and facile synthesis of substituted cinnoline and benzo[h]cinnoline. Tetrahedron Lett., 44, 3493-3496.
10. Al-Mousawi S. M., Moustafa M. S., Meier H., Kolshorn H., and Elnagdi M. H. (2009) Polyfunctional Nitriles in Organic Syntheses: A Novel Route to Aminopyrroles, Pyridazines and Pyrazolo[3,4-c]pyridazines. Molecules, 14, 798-806.
11. Abdelrazek F. M., Fadda A. A., and Elsayed A. N. (2011) Novel Synthesis of Some New Pyridazine and Pyridazino[4,5-d]pyridazine Derivatives. Synth. Com., 41, 1119-1126.
12. Eicher T., and Hauptmann S. (2003) The Chemistry of Heterocycles, 2nd Ed, Wiely-VCH Veriag GmbH, 392.
13. Tisler M., and Stanovnik R. (1968) Pyridazines. Adv. Heterocycl. Chem., 9, 211-320.
14. Schmidt P., and Druey J. (1954) Heilmittelchemische Studien in der heterocyclischen Reihe. 5. Mitteilung. Pyridazine II. Eine neue Pyridazinsynthese. Helv. Chim. Acta., 37, 134-140.
15. Khalafy J., Rimaz M., Ezzati M., and Prager R. H. (2012) A Green One-Pot Protocol for Regioselective Synthesis of New Substituted 7,8-Dihydrocinnoline-5(6H)-ones, Bull. Korean Chem. Soc., 33, 2890-2896.
16. Khalafy J., Rimaz M., Panahi L., and Rabiei H. (2011). A regiospecific one-pot, three component synthesis of 4-aryl-6,8-dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones as new potential monoamine oxidase inhibitors. Bull. Korean Chem. Soc., 32, 2428-2432.
17. Rimaz M., and Khalafy J. (2010) Novel one-pot, three component synthesis of alkyl 6-aryl-3-methylpyridazine-4-carboxylates in water. Arkivoc, ii, 110-117.
18. Rimaz M., Khalafy J., and Najafi Moghadam P. (2010) A regioselective one-pot, three component synthesis of 6-aryl-4-cyano-3(2H)-pyridazinones in water. Aust. J. Chem., 63, 1396-1401.
19. Rimaz M., Noroozi Pesyan N., and Khalafy J. (2010) Tautomerism and isotopic multiplets in the 13C-NMR spectra of partially deuterated 3-arylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones and their sulfur analogs-evidence for elucidation of the structure backbone and tautomeric forms. Magn. Reson. Chem., 48, 276-285.
20. Rimaz M., Khalafy J., Noroozi Pesyan N., and Prager R. H. (2010) A simple one-pot, three component synthesis of 3-arylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones and their sulfur analogues as potential monoamine oxidase inhibitors. Aust. J. Chem., 63, 507-510.
21. Khalafy J., Rimaz M., and Ezzati M. (2012) Regioselective one-pot, three component synthesis of ethyl 6-aryl-3-propylpyridazine-4-carboxylates in water, Curr. Chem. Lett., 1, 115-122.
22. Khalafy J., Parsa Habashi B., Poursattar Marjani A., and Najafi Moghadam P. (2012) The synthesis of 2-arylquinoxaline derivatives. Curr. Chem. Lett., 1, 139-46.
23. Khalafy J., Rimaz M., Farajzadeh S., and Ezzati M. (2013) A simple three-component synthesis of 3-amino-5-arylpyridazine-4-carbonitriles. S. Afri. J. Chem., 66, 179-182.
24. Riley H. A., and Gray A. R. (1943) Organic Syntheses, Collect. Vol. II, p. 509 (Wiley & Sons: New York, NY).
25. Bruker, SMART. Bruker AXS Inc., Madison, Wisconsin, USA 2002.
26. Bruker SAINT & SADABS. Bruker AXS Inc., Madison, Wisconsin, USA, 2008.
27. Sheldrick G. M. (2008) A short history of SHELX, Acta Crystallographica., A64, 112-122.
2. Rohet F., Rubat C., Coudert P., and Couquelet J. (1997) Synthesis and analgesic effects of 3-substituted 4,6-diarylpyridazine derivatives of the arylpiperazine class. Bioorg. Med. Chem., 5, 655-659.
3. Deeb A., Mourad E., and Elenany D. (2009) Pyridazine Derivatives and Related Compounds, Part 221: Synthesis, Reactions, and Insecticidal Activity of 3-Amino-5,6-diaryl-1H-pyrazolo[3,4-c]pyridazines. Phosphorus, Sulfur, and Silicon and the Related Elements., 185, 222-231.
4. Foks H., Wisterowicz K., Miszke A., Brozewicz K., Wisniewska K., and Dabrowska-Szponar M. (2009) Synthesis, Fungicidal and Antibacterial Activity of New Pyridazine Derivatives. Heterocycles., 78, 961-976.
5. Lamberth C., Trah S., Wendeborn S., Dumeunier R., Courbot M., Godwin J., and Schneiter P. (2012) Synthesis and fungicidal activity of tubulin polymerisation promoters. Part 2: Pyridazines. Bioorg. Med. Chem., 20, 2803–2810.
6. Smolyar N. N., Yutilov Yu. M., and Gres?ko, S. V. (2009) Synthesis of 4-amino-6-(hetaryl)pyridazin-3-ones as analogs of pyridazine-based cardiotonic agents. Pharm. Chem. J., 43, 87-88.
7. Ungureanu M., Mangalagiu I., Grosu G., and Petrovanu M. (1997) Antimicrobial activity of new pyridazine derivatives. Ann. Pharm. Fr., 55, 69-72.
8. Amer A. M., El-Mobayed M., Ateya A. M., and Muhdi T. S. (2002) On Condensation Reactions of Aceanthrene Quinone: Novel Heterocycles. Monatsh. Chem., 133, 79-88.
9. Gomaa M. Abdel-Motaal. (2003) An efficient and facile synthesis of substituted cinnoline and benzo[h]cinnoline. Tetrahedron Lett., 44, 3493-3496.
10. Al-Mousawi S. M., Moustafa M. S., Meier H., Kolshorn H., and Elnagdi M. H. (2009) Polyfunctional Nitriles in Organic Syntheses: A Novel Route to Aminopyrroles, Pyridazines and Pyrazolo[3,4-c]pyridazines. Molecules, 14, 798-806.
11. Abdelrazek F. M., Fadda A. A., and Elsayed A. N. (2011) Novel Synthesis of Some New Pyridazine and Pyridazino[4,5-d]pyridazine Derivatives. Synth. Com., 41, 1119-1126.
12. Eicher T., and Hauptmann S. (2003) The Chemistry of Heterocycles, 2nd Ed, Wiely-VCH Veriag GmbH, 392.
13. Tisler M., and Stanovnik R. (1968) Pyridazines. Adv. Heterocycl. Chem., 9, 211-320.
14. Schmidt P., and Druey J. (1954) Heilmittelchemische Studien in der heterocyclischen Reihe. 5. Mitteilung. Pyridazine II. Eine neue Pyridazinsynthese. Helv. Chim. Acta., 37, 134-140.
15. Khalafy J., Rimaz M., Ezzati M., and Prager R. H. (2012) A Green One-Pot Protocol for Regioselective Synthesis of New Substituted 7,8-Dihydrocinnoline-5(6H)-ones, Bull. Korean Chem. Soc., 33, 2890-2896.
16. Khalafy J., Rimaz M., Panahi L., and Rabiei H. (2011). A regiospecific one-pot, three component synthesis of 4-aryl-6,8-dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones as new potential monoamine oxidase inhibitors. Bull. Korean Chem. Soc., 32, 2428-2432.
17. Rimaz M., and Khalafy J. (2010) Novel one-pot, three component synthesis of alkyl 6-aryl-3-methylpyridazine-4-carboxylates in water. Arkivoc, ii, 110-117.
18. Rimaz M., Khalafy J., and Najafi Moghadam P. (2010) A regioselective one-pot, three component synthesis of 6-aryl-4-cyano-3(2H)-pyridazinones in water. Aust. J. Chem., 63, 1396-1401.
19. Rimaz M., Noroozi Pesyan N., and Khalafy J. (2010) Tautomerism and isotopic multiplets in the 13C-NMR spectra of partially deuterated 3-arylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones and their sulfur analogs-evidence for elucidation of the structure backbone and tautomeric forms. Magn. Reson. Chem., 48, 276-285.
20. Rimaz M., Khalafy J., Noroozi Pesyan N., and Prager R. H. (2010) A simple one-pot, three component synthesis of 3-arylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones and their sulfur analogues as potential monoamine oxidase inhibitors. Aust. J. Chem., 63, 507-510.
21. Khalafy J., Rimaz M., and Ezzati M. (2012) Regioselective one-pot, three component synthesis of ethyl 6-aryl-3-propylpyridazine-4-carboxylates in water, Curr. Chem. Lett., 1, 115-122.
22. Khalafy J., Parsa Habashi B., Poursattar Marjani A., and Najafi Moghadam P. (2012) The synthesis of 2-arylquinoxaline derivatives. Curr. Chem. Lett., 1, 139-46.
23. Khalafy J., Rimaz M., Farajzadeh S., and Ezzati M. (2013) A simple three-component synthesis of 3-amino-5-arylpyridazine-4-carbonitriles. S. Afri. J. Chem., 66, 179-182.
24. Riley H. A., and Gray A. R. (1943) Organic Syntheses, Collect. Vol. II, p. 509 (Wiley & Sons: New York, NY).
25. Bruker, SMART. Bruker AXS Inc., Madison, Wisconsin, USA 2002.
26. Bruker SAINT & SADABS. Bruker AXS Inc., Madison, Wisconsin, USA, 2008.
27. Sheldrick G. M. (2008) A short history of SHELX, Acta Crystallographica., A64, 112-122.