(C8H6N)CH(Ts)(4-NO2-C6H4)

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: (C8H6N)CH(Ts)(4-NO2-C6H4)
• 英文别名: 3-[(4-methylphenyl)sulfonyl-(4-nitrophenyl)methyl]-1H-indole
• 化学式: C₂₂H₁₈N₂O₄S
• 分子量: 406.462
• InChiKey: FUPYFSYEOIVORD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  29
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  104
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (C8H6N)CH(Ts)(4-NO2-C6H4) 、 N-二苯亚甲基-甘氨酸叔丁酯 在 (3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-(1-phenyl-ethyl)-amine 、 silver(I) chloride 、 caesium carbonate 作用下， 以 甲苯 为溶剂， 反应 24.08h， 以93%的产率得到(2S,3S)-tert-butyl-2-(diphenylmethyleneamino)-3-(1H-indol-3-yl)-3-(4-nitrophenyl)propanoate
  参考文献：
  名称：

  Ag-Catalyzed Diastereo- and Enantioselective Synthesis of β-Substituted Tryptophans from Sulfonylindoles

  摘要：

  The asymmetric catalytic synthesis of beta-substituted tryptophan derivatives was realized in high diastereo- and enantioselectivity by the reaction of glycine derivatives with sulfonylindoles in the presence of catalyst derived from AgCl and a commercially available chiral monodentate phosphoramidite ligand. The resulting adduct was readily converted to beta-substituted tryptophan in 95% overall yield for two steps, which presented a highly efficient route to chiral beta-substituted tryptophan.

  DOI：

  10.1021/ol100161n
• 作为产物：
  描述：

  吲哚 、 α-<4-Nitrophenyl>-N--urethan 在 montmorillonite K-10 作用下， 反应 15.0h， 以71%的产率得到(C8H6N)CH(Ts)(4-NO2-C6H4)
  参考文献：
  名称：

  Solventless Clay-Promoted Friedel−Crafts Reaction of Indoles with α-Amido Sulfones:  Unexpected Synthesis of 3-(1-Arylsulfonylalkyl) Indoles

  摘要：

  Friedel-Crafts reaction of indoles with alpha-amido sulfones in the presence of montmorillonite K-10 leads unexpectedly to 3-(1-arylsulfonylalkyl) indoles in good yield. The obtained products can be further desulfonylated under reductive or alkylative conditions giving linear and branched 3-substituted indoles.

  DOI：

  10.1021/ol061604w

文献信息

• Asymmetric Addition of α-Diazomethylphosphonate to Alkylideneindolenine Catalyzed by a Trifunctional BINAP-Based Monophosphonium Salt
  作者：Peng Zhu、Yi Yang、Yan Liu、Yungui Peng

  DOI：10.1021/acs.orglett.2c00213

  日期：2022.3.4

  were developed and used in the asymmetric addition of α-diazomethylphosphonates to vinylogous imines formed in situ from sulfonylindoles. This methodology tolerates a broad scope of 2-unsubstituted sulfonyl indoles, which have seldom achieved high enantioselectivities in similar asymmetric reactions with other nucleophiles. Chiral 3-sec-alkyl-substituted indoles containing α-diazophosphonate were afforded

  开发了一系列基于 BINAP 的三官能单鏻相转移催化剂，并用于将 α-重氮甲基膦酸酯不对称加成到由磺酰基吲哚原位形成的乙烯基亚胺中。这种方法可以容忍广泛的 2-未取代的磺酰基吲哚，它们在与其他亲核试剂的类似不对称反应中很少实现高对映选择性。以高达 99% 的产率和 95% 的ee提供了含有 α-重氮膦酸盐的手性 3 - sec-烷基取代的吲哚。
• Catalyst-free synthesis of 3-(1-arylsulfonylalkyl)indoles via three-component reaction of indoles, carbonyls, and arenesulfinic acids
  作者：Wenzhong Huang、Juan Yang、Xiangguang Li、Lin Yuan、Yinhai Ma、Qinglong Zhou、Deqiang Liang

  DOI：10.1080/10426507.2015.1100182

  日期：2016.5.3

  ABSTRACT A catalyst-free three-component reaction of indoles, carbonyls, and arenesulfinic acids performed at room temperature provides direct access to biologically important 3-(1-arylsulfonylalkyl)indoles. This process features mild conditions, low cost, broad substrate scope, and high yields, and mechanistically bis(indolyl)methanes were identified as the key intermediates. GRAPHICAL ABSTRACT

  摘要 在室温下进行的吲哚、羰基化合物和芳烃亚磺酸的无催化剂三组分反应提供了直接获得生物学上重要的 3-（1-芳基磺酰基烷基）吲哚的途径。该工艺具有条件温和、成本低、底物适用范围广、收率高等特点，在机理上双（吲哚基）甲烷被确定为关键中间体。图形概要
• Highly diastereo- and enantioselective synthesis of syn-β-substituted tryptophans via asymmetric Michael addition of a chiral equivalent of nucleophilic glycine and sulfonylindoles
  作者：Jiang Wang、Shengbin Zhou、Daizong Lin、Xiao Ding、Hualiang Jiang、Hong Liu

  DOI：10.1039/c1cc12619a

  日期：——

  The asymmetric synthesis of syn-beta-substituted tryptophan derivatives was carried out by the Michael addition of chiral equivalent of nucleophilic glycine with sulfonylindoles, and high diastereo- and enantioselectivities were achieved. The resulting adducts were readily converted to syn-beta-substituted tryptophans in 96% yield, indicating that the proposed method is a highly efficient route to

  通过将亲核甘氨酸的手性当量与磺酰吲哚的迈克尔加成，进行了β-取代色氨酸衍生物的不对称合成，并获得了高非对映选择性和对映选择性。所得的加合物易于以96％的产率转化为合成β-取代的色氨酸，表明所提出的方法是制备手性合成β-取代的色氨酸的高效途径。
• Solventless Clay-Promoted Friedel−Crafts Reaction of Indoles with α-Amido Sulfones:  Unexpected Synthesis of 3-(1-Arylsulfonylalkyl) Indoles
  作者：Roberto Ballini、Alessandro Palmieri、Marino Petrini、Elisabetta Torregiani

  DOI：10.1021/ol061604w

  日期：2006.8.1

  Friedel-Crafts reaction of indoles with alpha-amido sulfones in the presence of montmorillonite K-10 leads unexpectedly to 3-(1-arylsulfonylalkyl) indoles in good yield. The obtained products can be further desulfonylated under reductive or alkylative conditions giving linear and branched 3-substituted indoles.
• Ag-Catalyzed Diastereo- and Enantioselective Synthesis of β-Substituted Tryptophans from Sulfonylindoles
  作者：Bao-Hui Zheng、Chang-Hua Ding、Xue-Long Hou、Li-Xin Dai

  DOI：10.1021/ol100161n

  日期：2010.4.16

  The asymmetric catalytic synthesis of beta-substituted tryptophan derivatives was realized in high diastereo- and enantioselectivity by the reaction of glycine derivatives with sulfonylindoles in the presence of catalyst derived from AgCl and a commercially available chiral monodentate phosphoramidite ligand. The resulting adduct was readily converted to beta-substituted tryptophan in 95% overall yield for two steps, which presented a highly efficient route to chiral beta-substituted tryptophan.