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4-[2-(3-imino-3H-benzo[f]chromen-2-yl)thiazol-4-yl]-N,N-dimethylbenzenesulfonamide | 1180657-43-5

中文名称
——
中文别名
——
英文名称
4-[2-(3-imino-3H-benzo[f]chromen-2-yl)thiazol-4-yl]-N,N-dimethylbenzenesulfonamide
英文别名
4-[2-(3-iminobenzo[f]chromen-2-yl)-1,3-thiazol-4-yl]-N,N-dimethylbenzenesulfonamide
4-[2-(3-imino-3H-benzo[f]chromen-2-yl)thiazol-4-yl]-N,N-dimethylbenzenesulfonamide化学式
CAS
1180657-43-5
化学式
C24H19N3O3S2
mdl
——
分子量
461.565
InChiKey
DGRWEHAISTXJHG-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):
    4.8
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    120
  • 氢给体数:
    1
  • 氢受体数:
    7

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-[2-(3-imino-3H-benzo[f]chromen-2-yl)thiazol-4-yl]-N,N-dimethylbenzenesulfonamide盐酸溶剂黄146 作用下, 以 为溶剂, 反应 2.0h, 以79%的产率得到N,N-dimethyl-4-[2-(3-oxo-3H-benzo[f]chromen-2-yl)thiazol-4-yl]benzenesulfonamide
    参考文献:
    名称:
    Heteroaromatization with Sulfonamido Phenyl Ethanone, Part II: Synthesis of Novel Thiazolyl Acetonitriles and Thiazolyl Acrylonitriles and Their Derivatives Containing Dimethylsulfonamide Moiety
    摘要:
    Thiazolyl acetonitrile (2) was prepared and converted to pyrazolo[5,1-c][1,2,4]triazine (5), thiazoline-4-one derivatives (10,12), thiazolo[3,2-a]pyridine (13), coumarin (14), and benzo[f]coumarin (16) derivatives through reactions with a variety of organic electrophiles and nucleophiles. Thiazolyl acrylonitrile derivatives (17, 18, 21, 26-28, 31-33) were also prepared, and their activity with a variety of reagents was investigated. The structure of these compounds was elucidated on the basis of elemental analysis, IR, 1H-NMR, and mass spectra. The antimicrobial and antifungal activities of the prepared compounds are also reported.
    DOI:
    10.1080/10426500802176523
  • 作为产物:
    描述:
    4-(2-cyanomethylthiazol-4-yl)-N,N-dimethylbenzenesulfonamide2-羟基-1-萘甲醛哌啶 作用下, 以 乙醇 为溶剂, 反应 5.0h, 以80%的产率得到4-[2-(3-imino-3H-benzo[f]chromen-2-yl)thiazol-4-yl]-N,N-dimethylbenzenesulfonamide
    参考文献:
    名称:
    Heteroaromatization with Sulfonamido Phenyl Ethanone, Part II: Synthesis of Novel Thiazolyl Acetonitriles and Thiazolyl Acrylonitriles and Their Derivatives Containing Dimethylsulfonamide Moiety
    摘要:
    Thiazolyl acetonitrile (2) was prepared and converted to pyrazolo[5,1-c][1,2,4]triazine (5), thiazoline-4-one derivatives (10,12), thiazolo[3,2-a]pyridine (13), coumarin (14), and benzo[f]coumarin (16) derivatives through reactions with a variety of organic electrophiles and nucleophiles. Thiazolyl acrylonitrile derivatives (17, 18, 21, 26-28, 31-33) were also prepared, and their activity with a variety of reagents was investigated. The structure of these compounds was elucidated on the basis of elemental analysis, IR, 1H-NMR, and mass spectra. The antimicrobial and antifungal activities of the prepared compounds are also reported.
    DOI:
    10.1080/10426500802176523
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文献信息

  • Heteroaromatization with Sulfonamido Phenyl Ethanone, Part II: Synthesis of Novel Thiazolyl Acetonitriles and Thiazolyl Acrylonitriles and Their Derivatives Containing Dimethylsulfonamide Moiety
    作者:Saber M. Hassan、Mahmoud M. Abdel Aal、Ahmed A. El-Maghraby、Mahmoud S. Bashandy
    DOI:10.1080/10426500802176523
    日期:2009.2.3
    Thiazolyl acetonitrile (2) was prepared and converted to pyrazolo[5,1-c][1,2,4]triazine (5), thiazoline-4-one derivatives (10,12), thiazolo[3,2-a]pyridine (13), coumarin (14), and benzo[f]coumarin (16) derivatives through reactions with a variety of organic electrophiles and nucleophiles. Thiazolyl acrylonitrile derivatives (17, 18, 21, 26-28, 31-33) were also prepared, and their activity with a variety of reagents was investigated. The structure of these compounds was elucidated on the basis of elemental analysis, IR, 1H-NMR, and mass spectra. The antimicrobial and antifungal activities of the prepared compounds are also reported.
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