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
  • [41] An Efficient Synthesis of New 5-(1-Aryl-1H-pyrazole-4-yl)-1H-tetrazoles from 1-Aryl-1H-pyrazole-4-carbonitriles via [3+2] Cycloaddition Reaction
    dos Santos, Mauricio S.
    Bernardino, Alice M. R.
    Pinheiro, Luiz C. S.
    Canto-Cavalheiro, Marilene M.
    Leon, Leonor L.
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2012, 49 (06) : 1425 - 1428
  • [42] Microwave-Assisted Molybdenum-Catalyzed Reductive Cyclization of o-Nitrobenzylidene Amines to 2-Aryl-2H-indazoles
    Moustafa, Ahmed H.
    Malakar, Chandi C.
    Aljaar, Nayyef
    Merisor, Elena
    Conrad, Juergen
    Beifuss, Uwe
    SYNLETT, 2013, 24 (12) : 1573 - 1577
  • [43] MICROWAVE-ASSISTED PREPARATION OF 1D NCs FOR PHOTODEGRADATION PROCESS OF ORGANIC DYES
    Zaba, A.
    Matras-Postolek, K.
    Sovinska, S.
    Bogdal, D.
    17TH INTERNATIONAL CONFERENCE ON MICROWAVE AND HIGH FREQUENCY HEATING (AMPERE 2019), 2019, : 418 - 424
  • [44] SYNTHESIS OF 1-ARYL-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACIDS AND ESTERS
    BECK, JR
    WRIGHT, FL
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1987, 24 (03) : 739 - 740
  • [45] Thermal Effect in the Microwave-assisted Aminolysis of Benzoates and Amines
    Yang, Dongqiang
    Xu, Jiaxi
    CURRENT MICROWAVE CHEMISTRY, 2020, 7 (01) : 74 - 82
  • [46] N-arylsubstituted-1-aryl-3,4-diphenyl-5-pyrazole amines with analgesic and antiarrhythmic properties
    Bruno, O
    Schenone, S
    Ranise, A
    Bondavalli, F
    Falcone, G
    Filippelli, W
    Marabese, I
    Motula, G
    FARMACO, 1997, 52 (10): : 615 - 618
  • [47] Microwave-Assisted Cadogan Reaction for the Synthesis of 2-Aryl-2H-indazoles, 2-Aryl-1H-benzimidazoles, 2-Carbonylindoles, Carbazole, and Phenazine
    Cuevas Creencia, Evelyn
    Kosaka, Masahiro
    Muramatsu, Toshikatsu
    Kobayashi, Masashi
    Iizuka, Tomohiro
    Horaguchi, Takaaki
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2009, 46 (06) : 1309 - 1317
  • [48] Amidination of amines under microwave conditions using recyclable polymer-bound 1H-pyrazole-1-carboxamidine
    Solodenko, W
    Bröker, P
    Messinger, J
    Schön, U
    Kirschning, A
    SYNTHESIS-STUTTGART, 2006, (03): : 461 - 466
  • [49] Microwave-assisted synthesis of aryl and heteroaryl derivatives of benzimidazole
    Yu, H
    Kawanishi, H
    Koshima, H
    HETEROCYCLES, 2003, 60 (06) : 1457 - 1460
  • [50] One-pot, microwave-assisted synthesis of polymethylene-bridged bis (1H-1,2,4-triazol-5(3)-amines) and their tautomerism
    Lim, Felicia Phei Lin
    Hu, Lee Ming
    Tiekink, Edward R. T.
    Dolzhenko, Anton V.
    TETRAHEDRON LETTERS, 2018, 59 (42) : 3792 - 3796