Synthesis, structural characterization and antimicrobial evaluation of some novel piperidin-4-one oxime esters

被引:5
|
作者
Krishnan, K. Gokula [1 ]
Sivakumar, R. [1 ]
Thanikachalam, V. [1 ]
机构
[1] Annamalai Univ, Dept Chem, Annamalainagar 608002, Tamil Nadu, India
关键词
piperidin-4-one oxime; aromatic acid; mixed anhydride; gauche interaction; conformation; single crystal XRD; DERIVATIVES; INHIBITORS; ANALOGS;
D O I
10.2298/JSC141113037K
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fifteen novel biologically active piperidin-4-one oxime esters 8-22 were synthesized in good yields. These compounds were prepared in reactions of carboxylic acids, in situ activated using POCl3 and pyridine, with piperidin-4-one oximes. The structures of the title compounds were elucidated based on FTIR, NMR (1D and 2D) and mass spectral analyses. Single crystal XRD studies of compounds 12 and 20 provided further unambiguous evidence for the proposed structure. All the synthesized compounds were tested for their in vitro antibacterial and antifungal activities. Many of these derivatives exhibited good activity against Bacillus subtilis, Pseudomonas aeruginosa, Escherichia coli, Trichoderma viride and Aspergillus flavus.
引用
收藏
页码:1101 / +
页数:17
相关论文
共 50 条
  • [11] Synthesis, characterization, computational calculation and biological studies of some 2,6-diaryl-1-(prop-2-yn-1-yl)piperidin-4-one oxime derivatives
    Sundararajan, G.
    Rajaraman, D.
    Srinivasan, T.
    Velmurugan, D.
    Krishnasamy, K.
    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2015, 139 : 108 - 118
  • [12] An efficient synthesis of some substituted piperidin-4-one thiosemicarbazone derivatives as potential anticonvulsant under microwave irradiation
    Rastogi, Sameer
    Rastogi, Harshita
    INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 2010, 49 (05): : 547 - 553
  • [13] Design, synthesis, structural, in silico, and in vitro exploration of structurally modified hydrazones of piperidin-4-one with acetyl & ester moieties
    Karthiga, A. R.
    Divyabharathi, S.
    Shalo, R. Reshwen
    Rajeswari, K.
    Vidhyasagar, T.
    JOURNAL OF MOLECULAR STRUCTURE, 2025, 1322
  • [14] Novel asymmetric 3,5-bis(arylidene) piperidin-4-one derivatives: synthesis, crystal structures and cytotoxicity
    Yao, Binrong
    Li, Ning
    Wang, Chunhua
    Hou, Guige
    Meng, Qingguo
    Yan, Ke
    ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 2018, 74 : 659 - 665
  • [15] t-3-benzyl-r-2,c-6-bis(4-methoxyphenyl)-piperidin-4-one oxime
    Jayabharathi, J.
    Thangamani, A.
    Balamurugan, S.
    Thiruvalluvar, A.
    Linden, A.
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2008, 64 : O1211 - U1418
  • [16] In-silico molecular docking, ADMET and DFT evaluation of piperidin-4-one furoic hydrazone derivatives as antimicrobial, antioxidant and anticancer agents
    Sivanandhan, Monisha
    Seeman, Umamatheswari
    Parasuraman, Amutha
    JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2024, 21 (02) : 463 - 478
  • [17] In-silico molecular docking, ADMET and DFT evaluation of piperidin-4-one furoic hydrazone derivatives as antimicrobial, antioxidant and anticancer agents
    Monisha Sivanandhan
    Umamatheswari Seeman
    Amutha Parasuraman
    Journal of the Iranian Chemical Society, 2024, 21 : 463 - 478
  • [18] Synthesis, characterization, docking study and antiviral evaluation of new 3,5-Bis(benzylidene)piperidin-4-one Derivatives bearing phosphonate group
    Al Zahrani, Nourah A.
    JOURNAL OF MOLECULAR STRUCTURE, 2025, 1335
  • [19] Synthesis and Anti-leukemia Activity of 1-Substituted Piperidin-4-one Arylformylhydrazones
    Ni, Zhenjie
    Xue, Sijia
    Wang, Jing
    Meng, Weng
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2011, 31 (02) : 222 - 226
  • [20] Synthesis, spectral and antimicrobial evaluation of some novel 1-methyl-3-alkyl-2,6-diphenylpiperidin-4-one oxime carbonates
    Sivakumar, Rajamanickam
    Krishnan, Kannan Gokula
    Thanikachalam, Venugopal
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (11) : 3195 - 3199