Perchloric Acid Catalyzed Condensation of Amine and Aldehydes: Synthesis and Antibacterial Activities of Some Aryl (E)-Imines

Perumal Mayavel, Kannan Thirumurthy, Selladurai Dineshkumar, Ganesamoorthy Thirunarayanan

Abstract


A series of Schiff’s bases (aryl E-imines) have been derived from the perchloric acid catalyzed condensation of aryl amines and substituted benzaldehydes. The yield of the Schiff’s bases are more than 80%. The synthesized Schiff’s bases are characterized by their physical constants, analytical and spectroscopical data. The antibacterial activities of these Schiff’s bases have been studied using Bauer-Kirby method.

Full Text:

PDF

References


K.Y. Lau, A. Mayr, K.K. Cheung, Inorg. Chim. Acta, 285, 223, (1999).

A.S. Shawali, N.M.S. Harb, K.O. Badahdah, J. Heterocycl. Chem., 22, 1397, (1985).

S. France, M.H. Shah, A. Weatherwax, H. Wack, J.P. Roth, T. Lectka, J. Am. Chem. Soc., 127, 1206, (2005).

C.K.Z. Andrade, S.C.S. Takeda, L.M. Alves, J.P. Rodrigues, P.A.Z. Suarez, R.F. Brandao, V.C.D. Soares, Synlett, 12, 2135, (2004).

M. Abid, M. Savolainen, S. Landge, J. Hu, G.K. Surya Prakash, G.A. Olah, B. Torok, J. Fluorine Chem., 128, 587, (2007).

D.A. Barr, G. Donegn, R. Grigg, J. Chem. Soc. Perkin Trans. 1, 1550, (1989).

L. Blackburn, R.J.K. Taylor, Org. Lett., 3, 1637, (2001).

M. Gopalakrishnan, P. Sureshkumar, V. Kanagarajan, J. Thanusu, J. Res. Chem. Intermed., 33, 541, (2007). [9] R.T. McBurney, F. Portela-Cubillo, J.C. Walton, RSC Adv., 2, 1264, (2012).

A.K. Chakraborti, S. Bhagat, S. Rudrawar, Tetrahedron Lett., 45, 7641, (2004).

R.S. Varma, Green Chem., 1, 43, (1999).

A. Hasaninejad, A. Zare, H. Sharghi, M. Shekouhy, Arkivoc, 11, 64, (2008).

C.M. Bode, A. Ting, S.E. Schaus, Tetrahedron, 62, 11499, (2006).

M.A. Vazquez, M. Landa, L. Reyes, M.J. Tamariz, D. Francisco, Synth. Commun., 34, 2705, (2004).

M. Hudlicky, Oxidations in Organic Chemistry, ACS Monograph Series 186, American Chemical Society, Washington DC, (1990), p. 174.

S.M. Landge, V. Atanassova, M. Thimmaiah, B. Torok, Tetrahedron Lett., 48, 5161, (2007).

A. Kundu, N.A. Shakil, D.B. Saxena, J. Pankaj Kumar, S. Walia, J. Environ. Sci. Health B, 44, 428, (2009).

S.F. Martin, Pure Appl. Chem., 81, 195, (2009).

S.E. Denmark, G.L. Beutner, Angew. Chem. Int. Ed., 47, 1560, (2008).

P.K. Kabada, J. Heterocycl. Chem., 12, 143, (1975).

P.K. Kabada, J. Med. Chem., 31, 196, (1998).

D. Bandyopadhyay, S. Mukherjee, R.R. Rodriguez, B.K. Banik, Molecules, 15, 4207, (2010).

V. Tiwari, J. Meshram, P. Ali, Der. Pharm. Chem., 2, 187, (2010).

M. Sayyed, S. Mokle, M. Bokhare, A. Mankar, S. Surwase, S. Bhusare, Y. Vibhute, Arkivoc, 2, 187, (2006).

A.A. Bakibaev, V.K. Gorshkova, O.V. Arbit, V.D. Filimonov, A.S. Saratikov, Pharm. Chem. J., 28, 335, (1994).

S. Kantevari, T. Yempala, P. Yogeeswari, D. Sriram, B. Sridhar, Bioorg. Med. Chem. Lett., 21, 4316, (2011).

R. Yadav, S.D. Srivastava, S.K. Srivastava, Indian J. Chem., 44B, 1262, (2005).

B.W. Bauer, W.M.M. Kirby, J.C. Sherris, M. Truck, Am. J. Clin. Pathol., 45, 493, (1966).

R. Suresh, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, R. Sundararajan, S.P. Sakthinathan, S. Vijayakumar, K. Sathiyamoorthi, V. Mala, G. Vanangamudi, K. Thirumurthy, P. Mayavel, G. Thirunarayanan, Spectrochim. Acta A, 101, 239, (2013).




DOI: http://dx.doi.org/10.2478/umcschem-2013-0016
Date of publication: 2015-05-23 17:08:45
Date of submission: 2015-05-14 13:06:22


Statistics


Total abstract view - 1398
Downloads (from 2020-06-17) - PDF - 427

Indicators



Refbacks

  • There are currently no refbacks.


Copyright (c) 2015 Annales Universitatis Mariae Curie-Sklodowska, sectio AA – Chemia