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5,7-bibromo-2-phenyl-1H-indole | 5326-35-2

中文名称
——
中文别名
——
英文名称
5,7-bibromo-2-phenyl-1H-indole
英文别名
5,7-dibromo-2-phenyl-1H-indole;5,7-dibromo-2-phenyl-indole;5,7-Dibrom-2-phenyl-indol
5,7-bibromo-2-phenyl-1H-indole化学式
CAS
5326-35-2
化学式
C14H9Br2N
mdl
——
分子量
351.04
InChiKey
KLNUDQHISIUUAS-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):
    5.1
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    15.8
  • 氢给体数:
    1
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    5,7-bibromo-2-phenyl-1H-indole 在 Selectfluor 作用下, 以 乙醇 为溶剂, 反应 0.5h, 以0.049 g的产率得到5,7-dichloro-3,3-difluoro-2-phenyl-3H-indole
    参考文献:
    名称:
    One-Pot Gold-Catalyzed Aminofluorination of Unprotected 2-Alkynylanilines
    摘要:
    A tandem gold(I)-catalyzed aminocylization/fluorination and a two-step, one-pot gold(III)-catalyzed cyclization/electrophilic fluorination provide a convenient and general method for the synthesis of 3,3-difluoro-2-substituted-3H-indoles in good yield under mild conditions. Extension of the procedure to the synthesis of 2-aryl-3-fluoro-1H-indoles is described. The reaction proceeds smoothly in green ethanol and does not require any base, acid, or N-protective group.
    DOI:
    10.1021/ol401098b
  • 作为产物:
    描述:
    2,4-二氯-6-乙炔基苯胺 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodidesodium tetrachloroaurate(III) dihyrate二乙胺 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 12.5h, 生成 5,7-bibromo-2-phenyl-1H-indole
    参考文献:
    名称:
    One-Pot Gold-Catalyzed Aminofluorination of Unprotected 2-Alkynylanilines
    摘要:
    A tandem gold(I)-catalyzed aminocylization/fluorination and a two-step, one-pot gold(III)-catalyzed cyclization/electrophilic fluorination provide a convenient and general method for the synthesis of 3,3-difluoro-2-substituted-3H-indoles in good yield under mild conditions. Extension of the procedure to the synthesis of 2-aryl-3-fluoro-1H-indoles is described. The reaction proceeds smoothly in green ethanol and does not require any base, acid, or N-protective group.
    DOI:
    10.1021/ol401098b
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文献信息

  • The Development of a Palladium-Catalyzed Tandem Addition/Cyclization for the Construction of Indole Skeletons
    作者:Shuling Yu、Linjun Qi、Kun Hu、Julin Gong、Tianxing Cheng、Qingzong Wang、Jiuxi Chen、Huayue Wu
    DOI:10.1021/acs.joc.7b00148
    日期:2017.4.7
    A palladium-catalyzed tandem addition/cyclization of 2-(2-aminoaryl)acetonitriles with arylboronic acids has been developed for the first time, achieving a new strategy for direct construction of indole skeletons. This system shows good functional group tolerance and remarkable chemoselectivity. In particular, the halogen (e.g., bromo and iodo) substituents are amenable to further synthetic elaborations
    首次开发了钯催化的2-(2-氨基芳基)乙腈与芳基硼酸的串联串联加成/环化反应,实现了直接构建吲哚骨架的新策略。该系统显示出良好的官能团耐受性和出色的化学选择性。特别地,卤素(例如,溴和碘)取代基适合于进一步的合成精细化,从而扩大了产物的多样性。初步的机械实验表明,这种转化涉及相继的亲核加成,然后进行分子内环化。
  • Palladium-catalyzed tandem addition/cyclization in aqueous medium: synthesis of 2-arylindoles
    作者:Shuling Yu、Kun Hu、Julin Gong、Linjun Qi、Jianghe Zhu、Yetong Zhang、Tianxing Cheng、Jiuxi Chen
    DOI:10.1039/c7ob00572e
    日期:——
    was developed through palladium-catalyzed tandem addition/cyclization of potassium aryltrifluoroborates with aliphatic nitriles in aqueous medium. The use of water as the reaction medium makes the synthesis process environmentally benign. A plausible mechanism for the formation of 2-arylindoles involving sequential nucleophilic addition followed by an intramolecular cyclization is proposed. Moreover
    通过在水性介质中钯催化的芳基三氟硼酸钾与脂肪族腈的串联/串联加成/环化反应,开发了构建2-芳基吲哚的有效方案。使用水作为反应介质使合成过程对环境无害。提出了一个合理的机制,形成2-芳基吲哚涉及亲核加成顺序,然后进行分子内环化。此外,这种催化串联转化的效用也在有效的克级合成中得到了证明。该方法提供了另一种可替代的合成工具,可用于获得更多种类的2-芳基吲哚。
  • Process for production of vinyl chloride polymer
    申请人:Shin-Etsu Chemical Co., Ltd.
    公开号:EP0172427A2
    公开(公告)日:1986-02-26
    This process is a process for production of a vinyl chloride polymer by suspension polymerization or emulsion polymerization of vinyl chloride monomer or a mixture of vinyl chloride monomer with a vinyl monomer copolymerizable with said vinyl chloride monomer in an aqueous medium, characterized in that the polymerization is carried out in a polymerizer, the inner wall surface and portions of the auxiliary equipment thereof which may come into contact with the monomer during polymerization being previously coated with a scaling preventive comprising at least one selected from dyes, pigments and aromatic or heterocyclic compounds having at least 5 conjugated π bonds, while controlling the chloride ion concentration in the reaction mixture to not higher than 100 ppm. According to said process, scaling onto the inner wall surface of a polymerizer, etc. during polymerization can be prevented effectively and surely.
    该工艺是通过氯乙烯单体或氯乙烯单体与可与所述氯乙烯单体共聚的乙烯基单体混合物在水介质中进行悬浮聚合或乳液聚合来生产氯乙烯聚合物的工艺,其特征在于聚合是在聚合器中进行的、内壁表面及其辅助设备中可能在聚合过程中与单体接触的部分事先涂上一层防垢剂,该防垢剂至少包括一种选自染料、颜料和至少有 5 个共轭 π 键的芳香族或杂环化合物的防垢剂,同时控制反应混合物中的氯离子浓度不高于 100 ppm。根据上述工艺,可有效、可靠地防止聚合过程中聚合器等内壁表面结垢。
  • The Fischer Indole Synthesis. IV. Halogen Interchange during the Zinc Halide Induced Fischer Reactions of Acetophenone 2,6-Dihalophenylhydrazones<sup>1</sup>
    作者:Robert B. Carlin、Gerald W. Larson
    DOI:10.1021/ja01561a043
    日期:1957.2
  • US4757124A
    申请人:——
    公开号:US4757124A
    公开(公告)日:1988-07-12
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