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Synthesis of benzthiazole derivatives grouping with substituted azetidinone ring and its functional behaviour

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Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series of Schiff derivatives (5a-q) and azetidinone by way of amide linkage analogues (6a-q) containing 2-amino benzthiazole have been synthesized. Amide linkage were adapted from acid via reaction with hydrazine hydrate followed by reaction with different substituted aldehyde derived various Arylidene derivatives comprising with various donor and acceptor functional group. The structures of the new synthesized azetidinone derivatives were characterized on the basis of 1H-NMR, Mass, IR and elemental analysis data.
Słowa kluczowe
Rocznik
Strony
223--232
Opis fizyczny
Bibliogr. 16 poz., tab., wz.
Twórcy
  • Department of Chemistry (DST-FIST & UGC-SAP Funded), National Facility for Drug Discovery New Chemical Entities Development and Instrumentation Support to Small Manufacturing Pharma Enterprises, Saurashtra University, Rajkot - 360005, India
autor
  • Department of Chemistry (DST-FIST & UGC-SAP Funded), National Facility for Drug Discovery New Chemical Entities Development and Instrumentation Support to Small Manufacturing Pharma Enterprises, Saurashtra University, Rajkot - 360005, India
  • Department of Chemistry (DST-FIST & UGC-SAP Funded), National Facility for Drug Discovery New Chemical Entities Development and Instrumentation Support to Small Manufacturing Pharma Enterprises, Saurashtra University, Rajkot - 360005, India
autor
  • Department of Chemistry (DST-FIST & UGC-SAP Funded), National Facility for Drug Discovery New Chemical Entities Development and Instrumentation Support to Small Manufacturing Pharma Enterprises, Saurashtra University, Rajkot - 360005, India
Bibliografia
  • 1] Bradshaw, T. D.; Wrigley, S.; Shi, D. F.; Schulz, R. J.; Paull, K. D.; Stevens, M. F. G. Br., J. Cancer 77(1998) 745.
  • [2] Pratt, A. J.; Getzoff, E. D.; Perry J. J., Degener. Neurol. Neuromuscul. Dis. (2012) 1-14.
  • [3] Glicksman, M. A., Expert Opin. Drug Discov. 6 (2011) 1127-1138.
  • [4] Van Heusden, et al., J. Cancer 86 (2002) 605.
  • [5] Ali R., Siddiqui N. Journal of Chemistry 2013, Article ID 345198,12.
  • [6] Junne S.B., Kadam A. B., Zangade S. B., Shinde S. L. and Vibhute Y. B., International Multidisciplinary Research Journal 6 (2012) 44-47.
  • [7] Lourenco M.C.S., Souza M.V.N., Pinheiro A.C., Ferreira M.L., Goncalves R.S.B., Nogueira T.C.M., Peraltab M.A., Arkivoc 15 (2007) 181-191/
  • [8] Navin B. Patel, Jaymin C. Patel, Arabian Journal of Chemistry 4 (2011) 403-411.
  • [9] S. Sharma, V.K. Srivastava, A. Kumar, Eur. J. Med. Chem. 37 (2002) 689-697.
  • [10] P. Vicini, M. Incerti, I.A. Doytchinova, P.L. Colla, B. Busonera, R. Loddo,. J. Med. Chem. 41 (2006) 624-632.
  • [11] J.V. Ragavendran, D. Sriram, S.K. Patel, I.V. Reddy, N. Bharathwajan, J. Stables, P. Yogeeswari, Eur. J. Med. Chem. 42 (2007) 146-151.
  • [12] Alcaide B, Almendros P., Chem. Soc. Rev. 30 (2001) 226-240.
  • [13] Rajasekaran, A., Periasamy, M., Venkatesan, S., J Dev Bio and Tiss Eng. 2 (2010) 5.
  • [14] Pandey, V. K., Gupta, V. D., Upadhyay, M., Singh, V. K., Tandon, M.. Ind J Chem. 44 (2005) 158.
  • [15] Kagthara, P., Teja, S., Rajeev, D., Parekh, H. H., Ind J Hetero Chem. 10 (2000) 9.
  • [16] Mehta P. D., Sengar N. P. S., Subrahmanyam E. V. S.,Satyanarayana D., Ind J Pharm Sci. 68 (2006) 103.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-05f4b1ef-1028-435b-a0b9-855e69133689
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