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5-chloro-2-phenyl-1-tosyl-1H-indole

中文名称
——
中文别名
——
英文名称
5-chloro-2-phenyl-1-tosyl-1H-indole
英文别名
5-Chloro-1-(4-methylphenyl)sulfonyl-2-phenylindole;5-chloro-1-(4-methylphenyl)sulfonyl-2-phenylindole
5-chloro-2-phenyl-1-tosyl-1H-indole化学式
CAS
——
化学式
C21H16ClNO2S
mdl
——
分子量
381.883
InChiKey
VSVHOUQNAJFYSX-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):
    5.9
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    47.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2,4-二氯苯胺吡啶双(乙腈)氯化钯(II) 、 Cy-DHTP*HBF4lithium tert-butoxide 作用下, 以 二氯甲烷均三甲苯 为溶剂, 反应 4.17h, 生成 5-chloro-2-phenyl-1-tosyl-1H-indole
    参考文献:
    名称:
    One-Pot Synthesis of 2,4-Disubstituted Indoles fromN-Tosyl-2,3-dichloroaniline Using Palladium–Dihydroxyterphenylphosphine Catalyst
    摘要:
    4-Chloroindoles were synthesized from readily available 2,3-dichloroaniline derivatives and terminal alkynes. The catalyst composed of palladium and dicyclohexyl(dihydroxyterphenyl)phosphine (Cy-DHTP) enabled ortho-selective Sonogashira coupling, and subsequent cyclization afforded 4-chloroindoles in high yields. This transformation was successfully applied to the one-pot synthesis of 2,4-disubstituted indoles via Suzuki-Miyaura coupling after indole formation.
    DOI:
    10.1021/ol500711z
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文献信息

  • Silver(I)-Mediated CH Amination of 2-Alkenylanilines: Unique Solvent-Dependent Migratory Aptitude
    作者:So Won Youn、Tae Yun Ko、Min Jung Jang、Su San Jang
    DOI:10.1002/adsc.201400759
    日期:2015.1.12
    A highly effective silver(I)‐mediated CH amination of 2‐alkenylanilines has been developed to afford a diverse range of substituted indoles. High functional group tolerance, broad substrate scope, simple/fast/high‐yielding reaction, and recovery/reuse of the inexpensive silver oxidant are noteworthy. Furthermore, an uncommon migratory process of β‐monosubstituted 2‐alkenylanilines with solvent‐dependence
    已开发出一种高效的银(I)介导的2-烯基苯胺的CH胺化反应,以提供各种取代的吲哚。值得注意的是,高官能团耐受性,广泛的底物范围,简单/快速/高产率的反应以及廉价的银氧化剂的回收/再利用。此外,还证明了具有溶剂依赖性的β-单取代2-烯基苯胺的不常见迁移过程。
  • Et<sub>2</sub>Zn-Catalyzed Intramolecular Hydroamination of Alkynyl Sulfonamides and the Related Tandem Cyclization/Addition Reaction
    作者:Yan Yin、Wenying Ma、Zhuo Chai、Gang Zhao
    DOI:10.1021/jo070681h
    日期:2007.7.1
    Intramolecular hydroamination of alkynyl amides was effected by a catalytic amount of Et2Zn (20 mol %) to form indole derivatives, and a tandem cyclization/nucleophilic addition procedure involving reaction of the indole zinc salt intermediate with acid chlorides or halides was developed to provide an efficient approach to C3-substituted indole derivatives when an excess of Et2Zn (120 mol %) was used
    通过催化量的Et 2 Zn(20 mol%)进行炔酰胺的分子内加氢胺化反应,以形成吲哚衍生物,并开发了涉及吲哚锌盐中间体与酰氯或卤化物反应的串联环化/亲核加成方法,以提供当使用过量的Et 2 Zn(120 mol%)时,一种有效的C3取代的吲哚衍生物的方法。
  • Supported palladium nanoparticles-catalyzed decarboxylative coupling approaches to aryl alkynes, indoles and pyrrolines synthesis
    作者:C. Bal Reddy、Richa Bharti、Sandeep Kumar、Pralay Das
    DOI:10.1039/c6ra12046f
    日期:——
    The polystyrene supported palladium (Pd@PS) nanoparticles (NPs) catalyzed decarboxylative coupling (DC) of arylhalides and alkynyl carboxylic acids was developed for the synthesis of diaryl alkynes. Indole and 3-pyrroline heterocycles were also synthesized from 2-iodo anilines/amino benzocycloheptene bromide and alkynyl carboxylic acids, following a domino decarboxylative coupling-cyclization (DCC)
    聚苯乙烯负载的钯(Pd @ PS)纳米粒子(NPs)催化芳基卤化物和炔基羧酸的脱羧偶联(DC)用于合成二芳基炔烃。在相同的催化条件下,按照多米诺脱羧偶联-环化(DCC)方法,还从2-碘苯胺/氨基苯并环庚烯溴化物​​和炔基羧酸合成了吲哚和3-吡咯啉杂环。Pd @ PS的结合锚固和催化性能使该方法有利于产物的形成。
  • Facile synthesis of indoles by K 2 CO 3 catalyzed cyclization reaction of 2-ethynylanilines in water
    作者:Zhi Chen、Xiao-Xiao Shi、Dong-Qin Ge、Zhen-Zhen Jiang、Qi-Qi Jin、Hua-Jiang Jiang、Jia-Shou Wu
    DOI:10.1016/j.cclet.2016.07.022
    日期:2017.2
    Abstract The cyclization reaction of 2-ethynyl- N -sulfonylanilides proceeded efficiently in water with the presence of a catalytic amount of K 2 CO 3 under transition metal-free condition to give indoles in high yields. The recovery and reusability of the present catalytic system were investigated.
    摘要在无过渡金属条件下,在催化量的K 2 CO 3存在下,2-乙炔基-N-磺酰腈在水中的环化反应有效地进行,从而获得了高产率的吲哚。研究了本催化体系的回收率和可重复使用性。
  • DMSO/SOCl<sub>2</sub>-mediated C(sp<sup>2</sup>)–H amination: switchable synthesis of 3-unsubstituted indole and 3-methylthioindole derivatives
    作者:Jingran Zhang、Xiaoxian Li、Xuemin Li、Haofeng Shi、Fengxia Sun、Yunfei Du
    DOI:10.1039/d0cc07453e
    日期:——
    The reaction of 2-alkenylanilines with SOCl2 in DMSO was found to selectively afford 3-unsubstituted indoles and 3-methylthioindoles. This switchable approach was found to be temperature-dependent: at room temperature, the reaction afforded 3-unsubstituted indoles through intramolecular cyclization and elimination; while at higher temperature, the reaction gave 3-methylthioindoles via further electrophilic
    发现2-烯基苯胺与SOCl 2在DMSO中的反应选择性地提供3-未取代的吲哚和3-甲基硫代吲哚。发现这种可转换的方法是温度依赖性的:在室温下,该反应通过分子内环化和消除得到3-未取代的吲哚;在较高温度下,反应通过进一步的亲电甲基硫醇化反应生成3-甲基硫吲哚。
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