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1,3-diphenyl-5-(pyridin-4-yl)-1H-pyrazole | 37738-16-2

中文名称
——
中文别名
——
英文名称
1,3-diphenyl-5-(pyridin-4-yl)-1H-pyrazole
英文别名
1,3-Diphenyl-5-isonicotinylpyrazole;4-(2,5-diphenyl-2H-pyrazol-3-yl)-pyridine;4-(1,3-diphenyl-1H-pyrazol-5-yl)pyridine;4-(2,5-diphenylpyrazol-3-yl)pyridine
1,3-diphenyl-5-(pyridin-4-yl)-1H-pyrazole化学式
CAS
37738-16-2
化学式
C20H15N3
mdl
——
分子量
297.359
InChiKey
DRWKUZUAJDESPQ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    30.7
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    二硫代苯甲酸甲酯 在 sodium hydride 作用下, 以 乙醇N,N-二甲基甲酰胺 为溶剂, 反应 5.0h, 生成 1,3-diphenyl-5-(pyridin-4-yl)-1H-pyrazole
    参考文献:
    名称:
    Cyclocondensation of Arylhydrazines with 1,3-Bis(het)arylmonothio-1,3-diketones and 1,3-Bis(het)aryl-3-(methylthio)-2-propenones: Synthesis of 1-Aryl-3,5-bis(het)arylpyrazoles with Complementary Regioselectivity
    摘要:
    Two efficient highly regioselective routes for the synthesis of unsymmetrically substituted 1-aryl-3,5-bis(het)arylpyrazoles with complementary regioselectivity starting from active methylene ketones have been reported. In the first protocol, the newly synthesized 1,3-bis(het)aryl-monothio-1,3-diketone precursors (prepared by condensation of active methylene ketones with het(aryl) dithioesters in the presence of sodium hydride) were reacted with arylhydrazines in refluxing ethanol under neutral conditions, furnishing 1-aryl-3,5-bis(het)arylpyrazoles 7, in which the het(aryl) moiety attached to the thiocarbonyl group of monothio-1,3-diketones is installed at the 3-position. In the second method, the corresponding 3-(methylthio)-1,3-bis(het)aryl-2-propenones (prepared in situ by base-induced alkylation of 1,3-monothiodiketones) were condensed with arylhydrazines in the presence of potassium tert-butoxide in. refluxing tert-butyl alcohol, yielding 1-aryl-3,5-bis(het)arylpyrazoles 9 with complementary regioselectivity (method A). The efficiency of this protocol was further improved by developing a one-pot, three-component procedure for the synthesis of pyrazoles 9, directly from active methylene ketones, by reacting in situ generated 3-(methylthio)-1,3-bis(het)aryl-2-propenones with arylhydrazines in the presence of sodium hydride (instead of potassium tert-butoxide as base). The structures and regiochemistry of newly synthesized pyrazoles were confirmed from their spectral and analytical data along with X-ray crystallographic data of three pairs of regioisomers.
    DOI:
    10.1021/jo400599e
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文献信息

  • Fulmer, Tammy D.; Dasher, Lisette P.; Bobb, Bonni L., Journal of Heterocyclic Chemistry, 1980, vol. 17, p. 799 - 800
    作者:Fulmer, Tammy D.、Dasher, Lisette P.、Bobb, Bonni L.、Wilson, Jana D.、Sides, Kimberly L.、Beam, Charles F.
    DOI:——
    日期:——
  • FULMER T. D.; DASHER L. P.; BOBB B. L.; WILSON J. D.; SIDES K. L.; BEAM C+, J. HETEROCYCL. CHEM., 1980, 17, NO 4, 799-800
    作者:FULMER T. D.、 DASHER L. P.、 BOBB B. L.、 WILSON J. D.、 SIDES K. L.、 BEAM C+
    DOI:——
    日期:——
  • Methods and Compositions for the Treatment of RAS Associated Disorders
    申请人:Ratner Nancy
    公开号:US20120302581A1
    公开(公告)日:2012-11-29
    The instant disclosure relates to compositions that may be useful as therapeutic agents for the treatment of disorders associated or caused by Ras deregulation or dysregulation, for example, disorders associated with alterations in the NF1 gene such as neurofibromatosis type I, fungal infections such as those caused by Candida albicans , and proliferative disorders such as glioblastoma.
  • CASEIN KINASE 1delta (CK 1delta) INHIBITORS AND THEIR USE IN THE TREATMENT OF NEURODE-GENERATIVE DISEASES SUCH AS TAUOPATHIES
    申请人:Sheridan Joseph M.
    公开号:US20140031547A1
    公开(公告)日:2014-01-30
    The invention relates to pharmaceutical compositions comprising casein kinase 1 delta (CK1δ) and to the use of said inhibitors in the treatment of neurodegenerative disorders such as Alzheimer's disease.
  • CASEIN KINASE 1delta (CK 1delta) INHIBITORS AND THEIR USE IN THE TREATMENT OF NEURODEGENERATIVE DISEASES SUCH AS TAUOPATHIES
    申请人:Electrophoretics Limited
    公开号:US20160354375A1
    公开(公告)日:2016-12-08
    The invention relates to pharmaceutical compositions comprising casein kinase 1 delta (CK1δ) and to the use of said inhibitors in the treatment of neurodegenerative disorders such as Alzheimer's disease.
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