Microwave-Assisted Preparation of 1-Aryl-1H-pyrazole-5-amines

被引:0
|
作者
Law, Jarvis [1 ]
Manjunath, Aashrita [1 ]
Schioldager, Ryan [1 ]
Eagon, Scott [1 ]
机构
[1] Calif Polytech State Univ San Luis Obispo, Dept Chem & Biochem, San Luis Obispo, CA 93407 USA
来源
关键词
Chemistry; Issue; 148; pyrazole-5-amines; microwave synthesis; heterocycles; green chemistry; cyclization; phenylhydrazine; alpha-cyanoketone; 3-aminocrotononitrile; DERIVATIVES; DISCOVERY;
D O I
10.3791/59896
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A synthetic process for the preparation of a variety of 1-aryl-1H-pyrazole-5-amines was developed. The microwave-mediated nature of this method makes it efficient in both time and resources and utilizes water as the solvent. 3-Aminocrotononitrile or an appropriate a-cyanoketone is combined with an aryl hydrazine and dissolved in 1 M HCl. The mixture is then heated in a microwave reactor at 150 degrees C, typically for 10-15 min. The product can be readily obtained by basifying the solution with 10% NaOH and isolating the desired compound with a simple vacuum filtration. The use of water as a solvent in this reaction lends to its ease and utility in production, and this method is easily reproducible with a variety of functional groups. Typical isolated yields range from 70-90%, and reactions can be performed on the milligram to gram scale with little to no change in observed yields. Some of the applications of these molecules and their derivatives include pesticides, anti-malarials, and chemotherapeutics, among many others.
引用
收藏
页数:4
相关论文
共 50 条
  • [31] Halogenations of 3-Aryl-1 H -pyrazol-5-amines
    He, Jing
    Wei, Yueting
    Feng, Yijiao
    Li, Chuntian
    Dai, Bin
    Liu, Ping
    SYNTHESIS-STUTTGART, 2022, 54 (07): : 1793 - 1802
  • [32] Microwave-assisted preparation of 1,4-dihydropyridines from 1,3-diones and hexamethylenetetramine
    Hannon, Mary T.
    Sommer, Roger D.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [33] Microwave-assisted preparation of affinity medium
    Solanki, Kusum
    Mondal, Kalyani
    Gupta, Munishwar N.
    ANALYTICAL BIOCHEMISTRY, 2007, 360 (01) : 123 - 129
  • [34] Microwave-assisted preparation of silver nanoparticles
    Yamamoto, T
    Wada, Y
    Sakata, T
    Mori, H
    Goto, M
    Hibino, S
    Yanagida, S
    CHEMISTRY LETTERS, 2004, 33 (02) : 158 - 159
  • [35] Microwave-assisted preparation of aryltetrazoleboronate esters
    Schulz, MJ
    Coats, SJ
    Hlasta, DJ
    ORGANIC LETTERS, 2004, 6 (19) : 3265 - 3268
  • [36] Microwave-assisted preparation of titanate nanotubes
    Wang, YA
    Yang, JJ
    Zhang, JW
    Liu, HJ
    Zhang, ZJ
    CHEMISTRY LETTERS, 2005, 34 (08) : 1168 - 1169
  • [37] Microwave-assisted preparation of semiconducting polymers
    Galbrecht, Frank
    Buennagel, Torsten W.
    Scherf, Ullrich
    Farrell, Tony
    MACROMOLECULAR RAPID COMMUNICATIONS, 2007, 28 (04) : 387 - 394
  • [38] A convenient synthesis of 4(5)-(hetero)aryl-1H-imidazoles via microwave-assisted Suzuki-Miyaura cross-coupling reaction
    Vichier-Guerre, Sophie
    Dugue, Laurence
    Pochet, Sylvie
    TETRAHEDRON LETTERS, 2014, 55 (46) : 6347 - 6350
  • [39] Microwave-assisted oxidation of 1-substituted tetrazole-5-thiones
    Efimova, Yu. A.
    Artamonova, T. V.
    Hrabalek, A.
    Koldobskii, G. I.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2010, 46 (01) : 153 - 154
  • [40] Microwave-assisted oxidation of 1-substituted tetrazole-5-thiones
    Yu.A. Efimova
    T.V. Artamonova
    A. Hrabalek
    G. I. Koldobskii
    Russian Journal of Organic Chemistry, 2010, 46 : 153 - 154