4-(1-methyl-1H-pyrrol-2-yl)aniline | 1397709-49-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: 4-(1-methyl-1H-pyrrol-2-yl)aniline
• 英文别名: 4-(1-methylpyrrol-2-yl)phenylamine；4-(1-Methylpyrrol-2-yl)aniline
• CAS: 1397709-49-7
• 化学式: C₁₁H₁₂N₂
• 分子量: 172.23
• InChiKey: GOOWQKXUHFIGAS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  31
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  2-(4-nitrophenyl)-1H-pyrrole 在 铁粉 、 sodium hydride 、 氯化铵 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 1.5h， 生成 4-(1-methyl-1H-pyrrol-2-yl)aniline
  参考文献：
  名称：

  [EN] HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES
  [FR] INHIBITEURS DE BIOSYNTHÈSE D'HÉPARANE SULFATE POUR TRAITER DES MALADIES

  摘要：

  公开号：

  WO2016057834A9

文献信息

• Cyanopyrrole-phenyl progesterone receptor modulators and uses thereof
  申请人：McComas Cameron Casey

  公开号：US20070027125A1

  公开（公告）日：2007-02-01

  Progesterone receptor modulators of formula I, or a pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , and R 7 are as defined herein. These compounds are useful for contraception and hormone replacement therapy. Also provided are products containing these compounds.

  公式I的孕酮受体调节剂，或其药用盐， 其中R1，R2，R3，R4，R5，R6和R7如本文所定义。这些化合物对避孕和激素替代疗法有用。还提供含有这些化合物的产品。
• A case of chain propagation: α-aminoalkyl radicals as initiators for aryl radical chemistry
  作者：Timothée Constantin、Fabio Juliá、Nadeem S. Sheikh、Daniele Leonori

  DOI：10.1039/d0sc04387g

  日期：——

  The generation of aryl radicals from the corresponding halides by redox chemistry is generally considered a difficult task due to their highly negative reduction potentials. Here we demonstrate that α-aminoalkyl radicals can be used as both initiators and chain-carriers for the radical coupling of aryl halides with pyrrole derivatives, a transformation often employed to evaluate new highly reducing

  通过氧化还原化学法从相应的卤化物产生芳基通常被认为是一项艰巨的任务，因为它们的还原电位很高。在这里，我们证明了α-氨基烷基自由基既可以用作引发剂，也可以用作链载体，用于芳基卤化物与吡咯衍生物的自由基偶联，这种转化通常用于评估新型的高度还原性光催化剂。这种反应方式避免了使用强还原性物质，并且还可以形成sp 2 C–P键。机理研究描述了触发芳基自由基生成并传播链过程的一些关键特征。
• Cyanopyrrole-phenyl amide progesterone receptor modulators and uses thereof
  申请人：McComas Cameron Casey

  公开号：US20080064673A1

  公开（公告）日：2008-03-13

  Progesterone receptor modulators of formula I, or a pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined herein. These compounds are useful for contraception and hormone replacement therapy. Also provided are products containing these compounds.

  公开了一种化学式I的孕激素受体调节剂，或其药学上可接受的盐，其中R1、R2、R3、R4、R5、R6和R7的定义如本文所述。这些化合物对于避孕和激素替代疗法有用。还提供了含有这些化合物的产品。
• Palladium-Catalysed Direct Arylation of Heteroaromatics Using Unprotected Iodoanilines with Inhibition of the Amination Reaction
  作者：Hamed Ammar、Henri Doucet、Anissa Beladhria、Kassem Beydoun、Ridha Salem

  DOI：10.1055/s-0031-1291124

  日期：2012.7

  The palladium-catalysed direct arylation of heteroaromatics with unprotected iodoanilines proceeds in moderate to high yields using only 1 mol% Pd(OAc)(2) as the catalyst and potassium acetate as the base. No amination reaction was observed under these conditions. A wide variety of heteroarenes have been successfully employed.
• HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES
  申请人：BioMarin Pharmaceutical Inc.

  公开号：US20190151312A1

  公开（公告）日：2019-05-23

  Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions in need of inhibition of heparan sulfate biosynthesis.