Ionic liquid catalyzed one pot green synthesis of isoxazolone derivatives via multicomponent reaction

被引:0
|
作者
Shirole, G. D. [1 ]
Tambe, A. S. [1 ]
Shelke, S. N. [2 ,3 ]
机构
[1] ASC Coll, Dept Chem, Rahata, India
[2] Dada Patil Mahavidyalaya, Dept Chem, Karjat 414402, India
[3] Univ Pune, Pune, Maharashtra, India
关键词
1,3-Diaryl-1H-pyrazole-4-carboxyaldehyde; isoxazolone; ionic liquid; ultrasound; microwave; MICROWAVE IRRADIATION; IMIDAZOLE DERIVATIVES; EFFICIENT SYNTHESIS; IN-VITRO; 3,4-DIHYDROPYRIMIDIN-2(1H)-ONES; CYCLOADDITION; PROTOCOL;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of 3-methyl-4-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)isoxazol-5(4H)-one derivatives have been efficiently synthesized by environmentally benign, one-pot three component condensation of substituted 1,3-diaryl-1H-pyrazole-4-carboxyaldehyde, beta-keto ester and hydroxyl amine hydrochloride in the presence of ionic liquid [HNMP][HSO4] as a catalyst in ethanol. These derivatives have been synthesized by conventional, ultrasound and microwave irradiation methods. The combination of ionic liquid with ultrasound as well as microwave irradiation makes the protocol fascinating and environmentally benign. In addition, it has several benefits such as simple work-up procedure, clean reaction profile, short reaction time and good yields.
引用
收藏
页码:459 / 464
页数:6
相关论文
共 50 条
  • [21] Green synthesis of naphthyridine derivatives in ionic liquid via three-component reaction
    Jing Xu
    Yi-Sen Cao
    Yu-Ling Li
    Yun Liu
    Xiang-Shan Wang
    Research on Chemical Intermediates, 2015, 41 : 3873 - 3884
  • [22] [BCMIM][Cl] ionic liquid catalyzed diastereoselective synthesis of β-amino ketones via facile, one-pot, multicomponent Mannich reaction under solvent-free condition
    Mohurle, Shital
    Devi, C. Vishnu
    Pasuparthy, Sai Deepak
    Talamarla, Deepthi
    Kali, Venkatesan
    Maiti, Barnali
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2023, 60 (09) : 1545 - 1557
  • [23] Ionic liquid catalyzed one pot four-component coupling reaction for the synthesis of functionalized pyrroles
    Gupta, Neeru
    Singh, Kamal N.
    Singh, Jasvinder
    JOURNAL OF MOLECULAR LIQUIDS, 2014, 199 : 470 - 473
  • [24] Synthesis of novel spirooxindole derivatives by one pot multicomponent reaction and their antimicrobial activity
    Bhaskar, Gangaru
    Arun, Yuvaraj
    Balachandran, Chandrasekar
    Saikumar, Chandrasekara
    Perumal, Paramasivan T.
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2012, 51 : 79 - 91
  • [25] Synthesis of pyrimidine derivatives via multicomponent reaction catalyzed by ferric chloride
    Xian, Liang
    Ma, Cui-Ting
    Ouyang, Ying-Gen
    Di, Jia-Qi
    Zhang, Zhan-Hui
    APPLIED ORGANOMETALLIC CHEMISTRY, 2020, 34 (11)
  • [26] Glycine and its derivatives catalyzed one-pot multicomponent synthesis of bioactive heterocycles
    Kaur, Manmeet
    Priya, Anu
    Sharma, Aditi
    Singh, Arvind
    Banerjee, Bubun
    SYNTHETIC COMMUNICATIONS, 2022, 52 (16) : 1635 - 1656
  • [27] One-Pot Synthesis of Spirooxazino Derivatives via EnzymeInitiated Multicomponent Reactions
    Wang, Jun-Liang
    Chen, Xiao-Yang
    Wu, Qi
    Lin, Xian-Fu
    ADVANCED SYNTHESIS & CATALYSIS, 2014, 356 (05) : 999 - 1005
  • [28] Green One-Pot Asymmetric Synthesis of Peptidomimetics via Sequential Organocatalyzed Aziridination and Passerini Multicomponent Reaction
    dos Santos, Deborah A.
    da Silva, Allan R.
    Ellena, Javier
    da Silva, Cecilia C. P.
    Paixao, Marcio W.
    Correa, Arlene G.
    SYNTHESIS-STUTTGART, 2020, 52 (07): : 1076 - 1086
  • [29] Green Synthesis of Novel Pyridines via One-Pot Multicomponent Reaction and Their Anti-Inflammatory Evaluation
    El-Lateef, Hany M. Abd
    Abdelhamid, Antar A.
    Khalaf, Mai M.
    Gouda, Mohamed
    Elkanzi, Nadia. A. A.
    El-Shamy, Hemdan
    Ali, Ali M.
    ACS OMEGA, 2023, 8 (12): : 11326 - 11334
  • [30] Ionic liquid-catalyzed green synthesis of cyclohexanone diesters via double addition reaction
    Pourian, Somayeh
    Ashouri, Akram
    RESEARCH ON CHEMICAL INTERMEDIATES, 2025, 51 (03) : 1341 - 1355