Abstract
The formation of metal complexes with acid hydrazides plays an important role in the growth of their biological activity. A simple synthetic strategy is described for the synthesis of novel 1,2,4-tri-azepine and 1,2,5-triazocine derivatives via electron donor–acceptor interaction. Thus when 2-aminobenzohydrazide reacted with tetracyanoethylene (TCNE) and 2-dicyanomethylene-indan-1,3-dione (CNIND) afforded 1,2,4-triazepine derivatives. While on reacting
References
1.
Miyazawa J.
,
Kawabata T.
, and
Ogasawara N.
, Physiol. Mol. Plant Pathol. , 1998 , 52 , 115 .
2.
Imam I.
,
Mandour A.
, and
Abd El-Azeem F.
, Orient. J. Chem. , 1992 , 8 , 160 .
3.
Sammaiah G.
,
Brahmeshwar G.
, and
Sarangapani M.
, J. Adv. Pharm. Sci. , 2011 , 1 , 111 .
4.
Singh B.
,
Srivastava R.
, and
Narang K.K.
, Synth. React. Inorg Met.-Org. Chem. , 2000 , 30 , 1175 .
5.
Narang K.K.
, and
Singh V.P.
, Synth. React. Inorg. Met.-Org. Chem. , 1993 , 23 , 971 .
6.
Cymerman-Craig J.
,
Willis D.
,
Rubbo S.P.
, and
Edgar S.
, Nature , 1995 , 176 , 34 .
7.
Malhorta R.
,
Kumar S.
, and
Dhidsa K.S.
, Ind. J. Chem. , 1993 , 32A , 5457 .
8.
Muhi-Eldeen Z.
,
Al-Obidi K.
,
Nadir M.
, and
Rochev F.
, Eur. J. Med. Chem. , 1992 , 27 , 101 .
9.
Abdelwahed M.G.
,
Adelwanees S.
,
Elgamel M.
, and
Abdelhaleem S.
, J. Serb. Chem. Soc. , 2004 , 69 , 255 .
10.
Smirnov G.A.
,
Sizova E.P.
,
Luk'yanov O.A.
,
Fedyanin I.V.
, and
Antipin M.Y.
, Russ. Chem. Bull. Intern. Ed. , 2003 , 52 , 2444 .
11.
Rezessy B.
,
Zubovics Z.
,
Kovacs J.
, and
Toth G.
, Tetrahedron , 1999 , 55 , 5909 .
12.
Ryng S.
,
Zimecki M.
,
Mczynski M.
,
Chodaczek G.
, and
Kociêba M.
, Pharm. Rep. , 2005 , 57 , 195 .
13.
Verardo G.
,
Toniutti N.
,
Gorassini A.
, and
Giumanini A.G.
, Eur. J. Org. Chem. , 1999 , 11 , 2943 .
14.
Yamamoto Y.
,
Shindo M.
, and
Nakamura T.
, PCT Int. Appl. WO 9747622 1998 [Chem. Abstr. 1998 , 128 , 75427 ].
15.
Sladowska H.
,
Bodetko M.
,
Sieklucka-Dziuba M.
,
Rajtar G.
,
Ziolkowska D.
, and
Kleinrok Z.
, Farmaco , 1997 , 52 , 657 .
16.
Dabholkar V.V.
, and
Moris G.D.
, Ind. J. Chem. , 2004 , 43b , 6824 .
17.
Sewell P.
,
Hawking F.
, and
Brit F.
, J. Pharmacol. , 1950 , 5 , 239 .
18.
Sayed A.A.R.
,
El-Shaieb K.M.
, and
Mourad A.-F.E.
, Arch. Pharm. Res. , 2012 , 35 , 69 .
19.
El-Shaieb K.M.
,
Hopf H.
, and
Jones P.G.
, Z. Naturforsch. , 2009 , 64b , 858 .
20.
El-Shaieb K.M.
J. Chin Chem. Soc. , 2008 , 55 , 1150 .
21.
Aly A.A.
, and
El-Shaieb K.M.
, J. Chem. Res. , 2007 , 207 .
22.
El-Shaieb K.M.
, J. Sulfur Chem. , 2007 , 28 , 223 .
23.
Abdel-Latif F.F.
,
El-Shaieb K.M.
, and
El-Deen A.G.
Z. Naturforsch. , 2011 , 66b , 965 .
24.
El-Shaieb K.M.
, J. Chem. Res. , 2010 , 34 , 137 .
25.
Abdel-Latif F.F.
,
El-Shaieb K.M.
, and
El-Deen A.G.
, J. Chem. Res. , 2010 , 34 , 449 .
26.
El-Shaieb K.M.
,
Abdel-Latif F.F.
, and
El-Din A.G.
, J. Chem. Res. , 2012 , 36 , 308 .
27.
El-Shaieb K.M.
,
Hassan A.A.
, and
Abdel-Aal A.S.
, J. Chem. Res. , 2011 , 35 , 592 .