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Synthesis of Novel Pyridazinonylbenzotriazoles
Corresponding Author(s) : S. Shashidhar Reddy
Asian Journal of Chemistry,
Vol. 27 No. 10 (2015): Vol 27 Issue 10
Abstract
4-Chlorobenzaldehyde (1) was reacted with crotononitrile (2) in the presence of sodium cyanide yielding 4-(4-chlorophenyl)-3-methyl-4-oxobutyronitrile (3) which on refluxing with concentrated HCl gave 4-(4-chlorophenyl)-3-methyl-4-oxobutyric acid (4). The latter, on treatment with fuming nitric acid, yielded 4-(4-chloro-3-nitrophenyl)-3-methyl-4-oxobutyric acid (5), which on treatment with hydrazine hydrate gave 6-(4-chloro-3-nitrophenyl)-5-methyl-4,5-dihydro-2H-pyridazine-3-one (6). Azidation and reduction of 6 with sodium azide gave the amino derivative 7 which on reductive alkylation gave 10(a-i) followed by reduction with commercially available sodium hydrogen sulphide solution gave the substituted diamine derivative 11(a-i). The compound 7 directly undergoes reduction with sodium hydrogen sulphide yielding (8). Finally, 8 and 11(a-i) was converted into the target compounds by diazotized-cyclization with sodium nitrite giving pyridazinonylbenzotriazoles 9 and 12( a-i).
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- E. Sotelo, N. Fraiz, M. Yáñez, R. Laguna, E. Cano and E. Raviña, Chem. Pharm. Bull. (Tokyo), 50, 1574 (2002); doi:10.1248/cpb.50.1574.
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A. Montero-Lastres, N. Fraiz, R. Laguna, E. Cano, I. Estevez and E. Ravina, Biol. Pharm. Bull., 22, 1376 (1999); doi:10.1248/bpb.22.1376.
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A.A. Siddiqui, S.R. Ahmad and S.A. Hussian, Acta Pol. Pharm., 64, 223 (2008).
A.A. Siddiqui, R. Mishra and M. Shaharyar, Eur. J. Med. Chem., 45, 2283 (2010); doi:10.1016/j.ejmech.2010.02.003.
W.V. Curran and A. Ross, J. Med. Chem., 17, 273 (1974); doi:10.1021/jm00249a004.
G. Szasz and Z. Budvavi-Bavauy, Pharmaceutical Chemistry of Antihypertensive Agents, CRC Press, Boca Raton, pp. 3-265 (1991).
G. Cignarella, D. Barlocco, G.A. Pinna, M. Loriga, M. Curzu, O. Tofanetti, M. Germini, P. Cazzulani and E. Cavalletti, Eur. J. Med. Chem., 32, 2277 (1989); doi:10.1021/jm00130a009.
A. Anees, A. Siddiqui, S.R. Ahmad, M. Shehroz, S. Akhtar, M. Raish and R. Kaur, Acta Pol. Pharm., 65, 223 (2008).
S.A. Abubshait, Molecules, 12, 25 (2007); doi:10.3390/12010025.
A.A. Ikizler and F. Ucar, Indian J. Heterocycl. Chem., 61, 271 (1999).
(a) H. Emilsson, H. Salendar and J. Gaarder, Eur. J. Med. Chem., 21, 333 (1985); (b) A. Monge, P. Parrado, M. Font and E. Fernandez-Alvarez, J. Med. Chem., 30, 1029 (1987); doi:10.1021/jm00389a012.
G.H. Sayed, M.A. Sayed, M.R. Mahmoud and S.S. Shaaban, Egypt. J. Chem., 45, 767 (2002).
R.R. Kassab, Egypt. J. Chem., 45, 1055 (2002).
M.F. Sahina, B. Badicoglu, M. Gökce, E. Küpeli and E. Yesilada, Arch. Pharm., 337, 445 (2004); doi:10.1002/ardp.200400896.
E. Banoglu, C. Akoglu, S. Unlu, E. Kupeli, E. Yesilada and M.F. Sahin, Arch. Pharm. Pharm. Med. Chem, 337, 7 (2004); doi:10.1002/ardp.200200738.
B. Okcelik, S. Unlu, E. Banoglu, E. Kupeli, E. Yesilada and M.F. Sahin, Arch. Pharm. Pharm. Med. Chem., 336, 406 (2003); doi:10.1002/ardp.200300778.
D.G.H. Livermore, R.C. Bethell, N. Cammack, A.P. Hancock, M.M. Hann, D.V.S. Green, R.B. Lamont, S.A. Noble and D.C. Orr, J. Med. Chem., 36, 3784 (1993); doi:10.1021/jm00076a005.
D.A. Williams and T.L. Lemke, Principles of Medicinal Chemistry, Lippincott Williams and Wilkins, edn 5 (2002).
M.S. Sudhir and R. VenkataNadh, J. Pharm. Res., 7, 47 (2013); doi:10.1016/j.jopr.2013.01.004.
A. Dubey, S.K. Srivastava and S.D. Srivastava, Bioorg. Med. Chem. Lett., 21, 569 (2011); doi:10.1016/j.bmcl.2010.10.057.
A.R. Katritzky, X. Lan, J.Z. Yang and O.V. Denisko, Chem. Rev., 98, 409 (1998); doi:10.1021/cr941170v.
D.W. Robertson, N.D. Jones, J.H. Krushinski, G.D. Pollock, J.K. Swartzendruber and J.S. Hayes, J. Med. Chem., 30, 623 (1987); doi:10.1021/jm00387a007.
D.W. Robertson, J.H. Krushinski, G.D. Pollock, H. Wilson, R.F. Kauffman and J.S. Hayes, J. Med. Chem., 30, 824 (1987); doi:10.1021/jm00388a014.
I. Sircar, R.E. Weishaar, D. Kobylarz, W.H. Moos and J.A. Bristol, J. Med. Chem., 30, 1955 (1987); doi:10.1021/jm00394a005.
V. Austel, J. Heider, W. Ebetlein, W. Diederne and W. Haarmann, Ger. Offen. DE, 2837161 (1978).
A. Bomhard, V. Austel, N. Hauel and W. Diederen, Actual. Chim. Ther., 16, 259 (1989).
F.J. McEvoy and G.R. Allen, J. Org. Chem., 38, 4044 (1973); doi:10.1021/jo00987a019.
J.D. Albright, F.M. McEvoy and D.B. Moran, J. Heterocycl. Chem., 15, 881 (1978); doi:10.1002/jhet.5570150601.
H. Stetter and M. Schrekenberg, Chem. Ber., 107, 210 (1974); doi:10.1002/cber.19741070127.
R. Jonas, M. Klockow, I. Lues, H. Prücher, H.J. Schliep and H. Wurziger, Eur. J. Med. Chem., 28, 129 (1993); doi:10.1016/0223-5234(93)90005-Y.
Y. Goriya and C.V. Ramana, Tetrahedron, 66, 7642 (2010); doi:10.1016/j.tet.2010.07.032.