1-(2-(3-bromophenyl)-2-oxoethyl)pyridin-1-ium bromide | 26031-67-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-(2-(3-bromophenyl)-2-oxoethyl)pyridin-1-ium bromide
• 英文别名: 1-[2-(3-Bromophenyl)-2-oxoethyl]pyridin-1-ium bromide；1-(3-bromophenyl)-2-pyridin-1-ium-1-ylethanone;bromide
• CAS: 26031-67-4
• 化学式: Br*C₁₃H₁₁BrNO
• 分子量: 357.044
• InChiKey: WAIHPYSAZRZQOW-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  -0.38
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  21
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(2-(3-bromophenyl)-2-oxoethyl)pyridin-1-ium bromide 在 1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 ammonium acetate 、 potassium acetate 、 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 1,4-二氧六环 、 甲醇 为溶剂， 反应 36.0h， 生成
  参考文献：
  名称：

  신규한 전자 수송 물질 및 이를 이용한 유기 발광 소자

  摘要：

  This invention relates to a novel electronic transport material and an organic light-emitting device including the same. By using the electronic transport material according to the present invention, it is possible to manufacture an organic light-emitting device with improved luminous characteristics and enhanced driving voltage, thereby inducing an increase in power efficiency and producing an organic light-emitting device with improved power consumption.

  公开号：

  KR101548686B1
• 作为产物：
  描述：

  吡啶 、 2,3-二溴苯乙酮 以 丙酮 为溶剂， 反应 10.0h， 生成 1-(2-(3-bromophenyl)-2-oxoethyl)pyridin-1-ium bromide
  参考文献：
  名称：

  含吡啶鎓盐的电子不足的烯烃的可见光诱导的Carbo-2-吡啶基化

  摘要：

  据报道，用容易获得的N-苯甲酰基甲基吡啶鎓溴化物，对缺电子的烯烃进行了简单，实用的可见光诱导的Carbo-2-吡啶基化。提出了40多个实例，并以优异的区域选择性和非对映选择性进行了平均收率超过80％的研究。

  DOI：

  10.1002/anie.201704385

文献信息

• DMAP-Catalyzed Annulation Approach for Modular Assembly of Furan-Fused Chromenes
  作者：Xinwei He、Ruxue Li、Pui Ying Choy、Tianyi Liu、Junya Wang、On Ying Yuen、Man Pan Leung、Yongjia Shang、Fuk Yee Kwong

  DOI：10.1021/acs.orglett.0c03374

  日期：2020.12.18

  With a tandem DMAP-catalyzed reaction between o-AQM, in which it is generated in situ from propargylic amine, and acyl carbene surrogate (from pyridinium ylide), a variety of polyarylated chromenes are assembled in good yields. This process does not require transition-metal catalyst and exhibits easy manipulation of the arene group and good functional group compatibility, particularly the −Br group

  通过邻位AQM（由炔丙基胺原位生成）和酰基卡宾替代物（由吡啶鎓内鎓盐）之间的串联DMAP催化反应，可以高收率组装各种聚芳基苯并二甲基苯酮。该方法不需要过渡金属催化剂，并且表现出对芳烃基团的容易操纵和良好的官能团相容性，特别是-Br基团，其可以通过交叉偶联反应进一步转化为其他官能团。o- AQM基板的模块化功能和简单的操作程序为该合成方法增加了更多优势。
• General and Direct Synthesis of Indolizine-1-carbaldehydes by 1,3-Dipolar Cycloaddition of Phenylpropiolaldehyde with Pyridinium Ylides
  作者：Tao Gao、Xiuling Chen、Longqiang Jiang、Minghu Wu、Haibing Guo、Jian Wang、Shaofa Sun、Jeremy Oiler、Yalan Xing

  DOI：10.1002/ejoc.201600945

  日期：2016.10

  An efficient and one-step synthesis of indolizine-1-carbaldehydes from phenylpropiolaldehyde and pyridinium ylides was developed. The elegant methodology afforded functionalized indolizines with easy operation under mild reaction conditions and with wide substrate scope.

  开发了一种从苯丙醛和吡啶鎓叶立德高效一步合成 indolizine-1-carbaldehydes 的方法。优雅的方法提供了功能化的吲哚嗪，在温和的反应条件下易于操作，底物范围广。
• Synthesis and biological activities of indolizine derivatives as alpha-7 nAChR agonists
  作者：Yu Xue、Jingshu Tang、Xiaozhuo Ma、Qing Li、Bingxue Xie、Yuchen Hao、Hongwei Jin、Kewei Wang、Guisen Zhang、Liangren Zhang、Lihe Zhang

  DOI：10.1016/j.ejmech.2016.03.016

  日期：2016.6

  Human α7 nicotinic acetylcholine receptor (nAChR) is a promising therapeutic target for the treatment of schizophrenia accompanied with cognitive impairment. Herein, we report the synthesis and agonistic activities of a series of indolizine derivatives targeting to α7 nAChR. The results show that all synthesized compounds have affinity to α7 nAChR and some give strong agonistic activity, particularly

  人α7烟碱乙酰胆碱受体（nAChR）是治疗伴有认知障碍的精神分裂症的有前途的治疗靶标。在本文中，我们报告了一系列针对α7nAChR的吲哚嗪衍生物的合成和激动活性。结果表明，所有合成的化合物均对α7nAChR具有亲和力，并且某些化合物具有很强的激动活性，特别是大多数活性激动剂均显示出比对照EVP-6124更高的效力。对接和结构-活性关系研究为开发更有效的新型α7nAChR激动剂提供了见识。
• 1,2-Dicarbofunctionalization of Trifluoromethyl Alkenes with Pyridinium Salts via a Cycloaddition/Visible-Light-Enabled Fragmentation Cascade
  作者：Shu-Jie Chen、Guo-Shu Chen、Tao Deng、Jia-Hui Li、Zhi-Qing He、Li-Shan Liu、Hai Ren、Yun-Lin Liu

  DOI：10.1021/acs.orglett.1c04148

  日期：2022.1.21

  Although trifluoromethyl alkenes have great synthetic potential, their 1,2-difunctionalization has been a challenge. In this Letter, we disclose the first 1,2-dicarbofunctionalization of trifluoromethyl alkenes with pyridinium salts via a cascade process involving a base-promoted [3 + 2] cycloaddition followed by a visible-light-mediated Norrish-type-II fragmentation. This protocol allows for the formation

  尽管三氟甲基烯烃具有巨大的合成潜力，但它们的 1,2-双官能化一直是一个挑战。在这封信中，我们公开了三氟甲基烯烃与吡啶鎓盐的第一个 1,2-二碳官能化反应，该反应通过一个级联过程进行，包括碱促进的 [3 + 2] 环加成，然后是可见光介导的 Norrish-II 型片段化。该协议允许在温和条件下以中等至优异的产率形成带有三氟甲基取代的季铵中心的吡啶。
• Bipiridine derivative and organic electroluminescence element containing the same
  申请人：Yamagata Promotional Organization for Industrial Technology

  公开号：EP2275409A1

  公开（公告）日：2011-01-19

  The present invention provides a new bipyridine derivative which is suitable for an electron transport material of an organic electronics element and which has bipyridyl central rings as a core, and further provides an organic electroluminescence element containing the derivative. The bipyridine derivative is expressed by the following general formula. (where A1, A2: represent an aromatic heterocyclic group (except for a carbazolyl group) and an aromatic hydrocarbon group and the aromatic heterocyclic group may be combined; a, b = 1 or 2; Ar1, Ar2: represent a divalent or trivalent aromatic hydrocarbon group which may be substituted by hydrogen atom, an alkyl group, a cycloalkyl group, or an alkoxy group; B1, B2: represent hydrogen atom, an alkyl group, a cycloalkyl group, an alkoxy group, an aromatic hydrocarbon group, or an aromatic heterocyclic group; and ring E1, ring E2: represent a pyridine ring, and may have hydrogen atom, an alkyl group, a cycloalkyl group, or an alkoxy group.), which is used as an electron transport material.

  本发明提供了一种新的联吡啶衍生物，适用于有机电子元件的电子传输材料，并且具有联吡啶中心环作为核心，并进一步提供了含有该衍生物的有机电致发光元件。联吡啶衍生物由以下一般公式表示（其中A1、A2：代表芳香杂环基团（除了吲哚基团）和芳香烃基团，芳香杂环基团可以结合；a，b = 1或2；Ar1，Ar2：代表可由氢原子、烷基、环烷基或烷氧基取代的二价或三价芳香烃基团；B1，B2：代表氢原子、烷基、环烷基、烷氧基、芳香烃基团或芳香杂环基团；环E1，环E2：代表吡啶环，并且可以具有氢原子、烷基、环烷基或烷氧基）。该衍生物用作电子传输材料。