Synthesis and pharmacological properties of some novel pyrazolidine and pyrazole derivatives

被引:0
|
作者
Bharat Parashar
Abhilasha Jain
Sudhir Bharadwaj
V. K. Sharma
机构
[1] Geetanjali College of Pharmacy,Microwave Chemistry Laboratory
[2] St. Xavier’s College,undefined
[3] College of Pharmacy,undefined
[4] University College of Science,undefined
来源
关键词
Synthesis; Microwave irradiation; Conventional heating; Isonicotinohydrazide; Ethyl 2-cyanoacetate; Hexane-2; 4-Dione; Pyrazolidine and pyrazole;
D O I
暂无
中图分类号
学科分类号
摘要
Microwave synthesis technique opens new avenues for the synthesis of many compounds. A novel and simple method has been developed for the synthesis of 1-(2,4-dinitrophenyl) pyrazolidine-3,5-dione and 1-(2,4-dinitrophenyl)-3,5-dimethyl-1H-pyrazole derivatives under microwave irradiation. These compounds exhibit mild to moderate antimircrobial activity against different strains of bacteria (e.g. E. coli,P.aeruginosa, S. aureus and B subtilis) and fungi (e.g. C. albicans and A. niger). All these synthesised compounds have been characterised by employing various techniques like TLC, Elemental analysis, IR, NMR and MS spectra. In addition to this, the yields of these compounds have been compared with the same compounds, obtained by conventional heating procedures. And the results show that by microwave irradiation method, the product yield is either high or may be same but it takes a very short period of time for reaction. Moreover, this technique provides ecofriendly or green chemical pathway for the synthesis of these compounds. Thus, the microwave irradiation method is more useful than the conventional method because of the shorter reaction time, better yield, conservation of energy and ecofriendly nature.
引用
收藏
页码:1692 / 1699
页数:7
相关论文
共 50 条
  • [21] Synthesis and Cytotoxicity Evaluation of Some Novel Tetrahydronaphthalene-Pyrazole Derivatives
    El-Karim, Somaia S. Abd
    Elsadek, M.
    Baraka, M.
    El-Zahar, M. I.
    Rabou, M. S. Abd
    EGYPTIAN JOURNAL OF CHEMISTRY, 2014, 57 (02): : 143 - 163
  • [22] Synthesis of some novel heterocyclic dyes derived from pyrazole derivatives
    Rizk, H. F.
    El-Badawi, M. A.
    Ibrahim, S. A.
    El-Borai, M. A.
    ARABIAN JOURNAL OF CHEMISTRY, 2011, 4 (01) : 37 - 44
  • [23] Synthesis and Pharmacological Activities of Pyrazole and Oxadiazole Derivatives: a Review
    Vahora, M. S.
    Boruah, J. J.
    Das, S. P.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2023, 59 (05) : 846 - 869
  • [24] Synthesis and Pharmacological Activities of Pyrazole and Oxadiazole Derivatives: a Review
    M. S. Vahora
    J. J. Boruah
    S. P. Das
    Russian Journal of Organic Chemistry, 2023, 59 : 846 - 869
  • [25] NOVEL SYNTHESIS OF PYRAZOLE AND PYRAZOLINE DERIVATIVES
    MATSUMURA, N
    KUNUGIHARA, A
    YONEDA, S
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1985, 22 (05) : 1169 - 1172
  • [26] Synthesis, pharmacological and biological screening of some novel pyrimidine derivatives
    Bhat, K. Ishwar
    Kumar, Abhishek
    Nisar, Muhammed
    Kumar, Pankaj
    MEDICINAL CHEMISTRY RESEARCH, 2014, 23 (07) : 3458 - 3467
  • [27] Synthesis, pharmacological and biological screening of some novel pyrimidine derivatives
    K. Ishwar Bhat
    Abhishek Kumar
    Muhammed Nisar
    Pankaj Kumar
    Medicinal Chemistry Research, 2014, 23 : 3458 - 3467
  • [28] Synthesis, optical properties and application of a set of novel pyrazole nopinone derivatives
    Yang, Jinlai
    Xu, Xu
    Rui, Jian
    Wang, Zhonglong
    Zhang, Yan
    Wang, Shifa
    Wu, Liangru
    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2017, 183 : 60 - 67
  • [29] SYNTHESIS AND PHARMACOLOGICAL PROPERTIES OF SOME DERIVATIVES OF P-AMINOPHENYLETHANOLAMINE
    TEOTINO, UM
    FRIZ, LP
    STEIS, G
    DELLABELLA, D
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 1963, 15 (01) : 26 - &
  • [30] A Review on Synthesis, Characterization, and Pharmacological Properties of Some Sydnone Derivatives
    Khan, Takallum
    Yadav, Ritu
    Kesharwani, Amul Kumar
    Chourasia, Karuna
    MINI-REVIEWS IN ORGANIC CHEMISTRY, 2025, 22 (04) : 359 - 380