3,5-BIS(TRIFLUOROMETHYL)PYRAZOLE AND SOME N-SUBSTITUTED DERIVATIVES

被引:41
|
作者
CLAIRE, PPK
COE, PL
JONES, CJ
MCCLEVERTY, JA
机构
[1] School of Chemistry, University of Birmingham, Birmingham, B15 2TT
关键词
D O I
10.1016/S0022-1139(00)80298-5
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The pyrazoles [CF3]2C3HN2R [R = H, COPh, C6F5, C6H4NO2-4 and C6H3[NO2]2-2,4] have been prepared in yields ranging from 27% [R = C6F5] to 78% [R = C6H3[NO2]2-2,4] by the reaction between 1,1,1,5,5,5-hexafluoropentane-2,4-dione and the appropriately substituted hydrazine, NH2NHR.
引用
收藏
页码:283 / 289
页数:7
相关论文
共 50 条
  • [41] THE EFFECT OF 3,5-DINITROBENZAMIDE AND ITS N-SUBSTITUTED DERIVATIVES ON COCCIDIOSIS IN CHICKENS
    MOREHOUSE, NF
    MCGUIRE, WC
    POULTRY SCIENCE, 1957, 36 (05) : 1143 - 1143
  • [42] Synthesis and Antimicrobial Activity of Some New N-Substituted Quinoline Derivatives of 1H-Pyrazole
    Thumar, Nilesh J.
    Patel, Manish P.
    ARCHIV DER PHARMAZIE, 2011, 344 (02) : 91 - 101
  • [43] NK1 RECEPTOR BINDING OF A FEW LOW MOLECULAR WEIGHT 3,5-BIS(TRIFLUOROMETHYL)BENZENE DERIVATIVES
    Lipinski, Piotr f. j.
    Matalinska, Joanna
    ACTA POLONIAE PHARMACEUTICA, 2023, 80 (03): : 363 - 372
  • [44] Adducts of triangular silver(i) 3,5-bis(trifluoromethyl)pyrazolate with thiophene derivatives: a weak interaction model of desulfurization
    Liu, Rongrong
    Zhang, Wenhua
    Wei, Donghui
    Chen, Jing-Huo
    Ng, Seik Weng
    Yang, Guang
    DALTON TRANSACTIONS, 2019, 48 (43) : 16162 - 16166
  • [45] An Efficient and Green Procedure for the Synthesis of Quinoxaline Derivatives using 3,5-Bis(trifluoromethyl)phenylammonium triflate (BFPAT) Organocatalyst
    Alipour, Mandana
    Hossaini, Zinatossadat
    Khaksar, Samad
    Rostami-Charati, Faramarz
    LETTERS IN ORGANIC CHEMISTRY, 2021, 18 (03) : 183 - 186
  • [46] Trinuclear Copper(I) and Silver(I) Adducts of 4-Chloro-3,5-bis(trifluoromethyl)pyrazolate and 4-Bromo-3,5-bis(trifluoromethyl)pyrazolate
    Hettiarachchi, Champika V.
    Rawashdeh-Omary, Manal A.
    Korir, Daniel
    Kohistani, Jehan
    Yousufuddin, Muhammed
    Dias, H. V. Rasika
    INORGANIC CHEMISTRY, 2013, 52 (23) : 13576 - 13583
  • [47] NITROGEN INVERSION IN N-SUBSTITUTED 2,2-BIS(TRIFLUOROMETHYL)AZIRIDINES
    KOSTYANOVSKY, RG
    TCHERVIN, II
    FOMICHOV, AA
    SAMOJLOV.ZE
    MAKAROV, CN
    ZEIFMAN, YV
    DYATKIN, BL
    TETRAHEDRON LETTERS, 1969, (46) : 4021 - +
  • [48] 3,5-bis(trifluoromethyl)phenyl sulfones in the direct Julia-Kocienski olefination
    Alonso, DA
    Fuensanta, M
    Nájera, C
    Varea, M
    JOURNAL OF ORGANIC CHEMISTRY, 2005, 70 (16): : 6404 - 6416
  • [49] 3,5-bis(trifluoromethyl)pyrazoles: A novel class of NFAT transcription factor regulator
    Djuric, SW
    BaMaung, NY
    Basha, A
    Liu, HQ
    Luly, JR
    Madar, DJ
    Sciotti, RJ
    Tu, NP
    Wagenaar, FL
    Wiedeman, PE
    Zhou, X
    Ballaron, S
    Bauch, J
    Chen, YW
    Chiou, XG
    Fey, T
    Gauvin, D
    Gubbins, E
    Hsieh, GC
    Marsh, KC
    Mollison, KW
    Pong, M
    Shaughnessy, TK
    Sheets, MP
    Smith, M
    Trevillyan, JM
    Warrior, U
    Wegner, CD
    Carter, GW
    JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (16) : 2975 - 2981
  • [50] SYNTHESIS OF ELECTRON-DEFICIENT SECONDARY PHOSPHINE OXIDES AND SECONDARY PHOSPHINES: BIS[3,5BIS(TRIFLUOROMETHYL) PHENYL] PHOSPHINE OXIDE and BIS[3,5-BIS( TRIFLUOROMETHYL) PHENYL] PHOSPHINE
    Busacca, Carl A.
    Lorenz, Jon C.
    Sabila, Paul
    Haddad, Nizar
    Senanayake, Chris H.
    ORGANIC SYNTHESES, 2007, 84 : 242 - +