2-cyclopropyl-1-(indolin-1-yl)ethan-1-one | 1353390-60-9

• 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: 2-cyclopropyl-1-(indolin-1-yl)ethan-1-one
• 英文别名: 2-Cyclopropyl-1-(indolin-1-yl)ethanone；2-cyclopropyl-1-(2,3-dihydroindol-1-yl)ethanone
• CAS: 1353390-60-9
• 化学式: C₁₃H₁₅NO
• 分子量: 201.268
• InChiKey: ZJZWWKSCYHNWCA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  2-cyclopropyl-1-(indolin-1-yl)ethan-1-one 在 吡啶 、 N-溴代丁二酰亚胺(NBS) 、 氨 、 氢气 作用下， 以 甲醇 、 水 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 20.0~70.0 ℃ 、4.0 MPa 条件下， 反应 104.0h， 生成 5-chloro-N-{[1-(cyclopropylacetyl)-2,3-dihydro-1H-indol-5-yl]methyl}thiophene-2-sulfonamide
  参考文献：
  名称：

  Identifying new lead structures to enhance tolerance towards drought stress via high-throughput screening giving crops a quantum of solace

  摘要：

  Novel synthetic lead structures interacting with RCAR/(PYR/PYL) receptor proteins were identified based on the results of a high-throughput screening campaign of a large compound library followed by focused SAR studies of the three most promising hit clusters. Whilst indolinylmethyl sulfonamides 8y,z and phenylsulfonyl ethylenediamines 9y,z showed strong affinities for RCAR/ (PYR/PYL) receptor proteins in wheat, thiotriazolyl acetamides 7f,s exhibited promising efficacy against drought stress in vivo (wheat, corn and canola) combined with confirmed target interaction in wheat and arabidopsis thaliana. Remarkably, binding affinities of several representatives of 8 and 9 were on the same level or even better than the essential plant hormone abscisic acid (ABA).

  DOI：

  10.1016/j.bmc.2019.115142
• 作为产物：
  描述：

  吲哚啉 、 ((cyclopropylethynyl)oxy)triisopropylsilane 在 对氟苯甲醇 、 三(4-甲氧苯基)膦 作用下， 以 甲苯 为溶剂， 以95%的产率得到2-cyclopropyl-1-(indolin-1-yl)ethan-1-one
  参考文献：
  名称：

  Three-component reaction discovery enabled by mass spectrometry of self-assembled monolayers

  摘要：

  多组分反应广泛应用于有机化学的许多领域。尽管取得了重大进展，但发现这种有利的转化仍具有挑战性。在此，我们介绍了一种并行、无标记反应发现平台的开发情况，该平台可用于鉴定新的多组分转化。我们的方法基于对自组装单层阵列上的界面化学反应进行平行质谱筛选。通过这种策略，我们发现了一种简单的有机膦，它可以催化硅氧炔、醛和胺的一种之前未知的缩合反应，以高效率和非对映选择性生成 3-羟基酰胺。利用溶液相方法对该反应进行了进一步优化。利用通用反应发现平台确定了一种新的多组分转化。这种方法需要利用质谱法快速分析自组装单层阵列上的界面化学反应。这样就能鉴定出一种简单的有机膦，它能催化一种以前未知的硅氧基炔、醛和胺的缩合反应。

  DOI：

  10.1038/nchem.1212

文献信息

• Free Amino Group Transfer via α‐Amination of Native Carbonyls
  作者：Minghao Feng、Anthony J. Fernandes、Ana Sirvent、Eleonora Spinozzi、Saad Shaaban、Nuno Maulide

  DOI：10.1002/anie.202304990

  日期：2023.7.10

  An amino group transfer strategy was developed to install free NH2 to the α-position of native carbonyls under mild conditions. The resulting primary α-aminated products are amenable to in situ peptide coupling or Pictet–Spengler cyclization in one-pot procedures. We anticipate this method to provide a general platform towards the synthesis of amines, ultimately opening exciting avenues in the synthesis

  开发了氨基转移策略以在温和条件下将游离NH 2安装到天然羰基的α位。所得初级 α-胺化产物适合在一锅程序中进行原位肽偶联或 Pictet-Spengler 环化。我们预计这种方法将为胺的合成提供一个通用平台，最终为肽模拟物的合成和医学研究开辟令人兴奋的途径。
• Identifying new lead structures to enhance tolerance towards drought stress via high-throughput screening giving crops a quantum of solace
  作者：Jens Frackenpohl、Linn Schneider、Luka J.B. Decker、Jan Dittgen、Franz Fenkl、Christian Fischer、Jana Franke、Joerg Freigang、Rahel Getachew、Susana M. Gonzalez Fernandez-Nino、Hendrik Helmke、Martin J. Hills、Sabine Hohmann、Jochen Kleemann、Karoline Kurowski、Gudrun Lange、Peter Luemmen、Nicole Meyering、Fabien Poree、Dirk Schmutzler、Sebastian Wrede

  DOI：10.1016/j.bmc.2019.115142

  日期：2019.12

  Novel synthetic lead structures interacting with RCAR/(PYR/PYL) receptor proteins were identified based on the results of a high-throughput screening campaign of a large compound library followed by focused SAR studies of the three most promising hit clusters. Whilst indolinylmethyl sulfonamides 8y,z and phenylsulfonyl ethylenediamines 9y,z showed strong affinities for RCAR/ (PYR/PYL) receptor proteins in wheat, thiotriazolyl acetamides 7f,s exhibited promising efficacy against drought stress in vivo (wheat, corn and canola) combined with confirmed target interaction in wheat and arabidopsis thaliana. Remarkably, binding affinities of several representatives of 8 and 9 were on the same level or even better than the essential plant hormone abscisic acid (ABA).
• Three-component reaction discovery enabled by mass spectrometry of self-assembled monolayers
  作者：Timothy J. Montavon、Jing Li、Jaime R. Cabrera-Pardo、Milan Mrksich、Sergey A. Kozmin

  DOI：10.1038/nchem.1212

  日期：2012.1

  Multicomponent reactions are employed extensively in many areas of organic chemistry. Despite significant progress, the discovery of such enabling transformations remains challenging. Here, we present the development of a parallel, label-free reaction-discovery platform that can be used in the identification of new multicomponent transformations. Our approach is based on parallel mass spectrometric screening of interfacial chemical reactions on arrays of self-assembled monolayers. This strategy enabled the identification of a simple organic phosphine that can catalyse a previously unknown condensation of siloxyalkynes, aldehydes and amines to produce 3-hydroxyamides with high efficiency and diastereoselectivity. The reaction was further optimized using solution-phase methods. A general reaction-discovery platform has been used for identification of a new multicomponent transformation. The approach entails rapid analysis of interfacial chemical reactions on arrays of self-assembled monolayers using mass spectrometry. This enabled identification of a simple organic phosphine that catalyses a previously unknown condensation of siloxy alkynes, aldehydes and amines.

  多组分反应广泛应用于有机化学的许多领域。尽管取得了重大进展，但发现这种有利的转化仍具有挑战性。在此，我们介绍了一种并行、无标记反应发现平台的开发情况，该平台可用于鉴定新的多组分转化。我们的方法基于对自组装单层阵列上的界面化学反应进行平行质谱筛选。通过这种策略，我们发现了一种简单的有机膦，它可以催化硅氧炔、醛和胺的一种之前未知的缩合反应，以高效率和非对映选择性生成 3-羟基酰胺。利用溶液相方法对该反应进行了进一步优化。利用通用反应发现平台确定了一种新的多组分转化。这种方法需要利用质谱法快速分析自组装单层阵列上的界面化学反应。这样就能鉴定出一种简单的有机膦，它能催化一种以前未知的硅氧基炔、醛和胺的缩合反应。