4-cyclopropyl-3-fluoroaniline | 1208083-48-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-cyclopropyl-3-fluoroaniline
• CAS: 1208083-48-0
• 化学式: C₉H₁₀FN
• mdl: MFCD14585553
• 分子量: 151.184
• InChiKey: XGGDMIHKUNLGQE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.333
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-cyclopropyl-3-fluoroaniline 、 联硼酸频那醇酯 在 亚硝酸特丁酯 作用下， 以 乙腈 为溶剂， 以48 %的产率得到2-(4-cyclopropyl-3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  参考文献：
  名称：

  [EN] CYCLOPROPYL-(HETERO)ARYL-SUBSTITUTED ETHYLSULPHONYLPYRIDINE DERIVATIVES
  [FR] DÉRIVÉS D'ÉTHYLSULFONYLPYRIDINE À SUBSTITUTION CYCLOPROPYLE- (HÉTÉRO)ARYLE

  摘要：

  The present invention relates to cyclopropyl-(hetero)aryl substituted ethylsulphonyl-pyridine derivatives of formula (I),wherein the variables are as defined in the description and in the claims, which can be used as antiparasitic agents for the treatment, prevention and/or control of parasitic infections and/or infestations in animals.

  公开号：

  WO2023036934A1
• 作为产物：
  描述：

  1-cyclopropyl-2-fluoro-4-nitrobenzene 在 铁粉 、 氯化铵 作用下， 以 甲醇 、 水 为溶剂， 以96 %的产率得到4-cyclopropyl-3-fluoroaniline
  参考文献：
  名称：

  [EN] CYCLOPROPYL-(HETERO)ARYL-SUBSTITUTED ETHYLSULPHONYLPYRIDINE DERIVATIVES
  [FR] DÉRIVÉS D'ÉTHYLSULFONYLPYRIDINE À SUBSTITUTION CYCLOPROPYLE- (HÉTÉRO)ARYLE

  摘要：

  The present invention relates to cyclopropyl-(hetero)aryl substituted ethylsulphonyl-pyridine derivatives of formula (I),wherein the variables are as defined in the description and in the claims, which can be used as antiparasitic agents for the treatment, prevention and/or control of parasitic infections and/or infestations in animals.

  公开号：

  WO2023036934A1

文献信息

• [EN] IDO INHIBITORS<br/>[FR] INHIBITEURS D'IDO
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2015031295A1

  公开（公告）日：2015-03-05

  There are disclosed compounds that modulate or inhibit the enzymatic activity of indoleamine 2,3-dioxygenase (IDO), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders, such as cancer, viral infections and/or autoimmune diseases utilizing the compounds of the invention.

  所公开的化合物能够调节或抑制吲哚胺2,3-双加氧酶（IDO）的酶活性，包含该化合物的药物组合物以及使用本发明的化合物治疗增殖性疾病的方法，如癌症、病毒感染和/或自身免疫疾病。
• [EN] INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF THEIR USE<br/>[FR] INHIBITEURS DE L'INDOLÉAMINE 2,3-DIOXYGÉNASE ET LEURS PROCÉDÉS D'UTILISATION
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2020023356A1

  公开（公告）日：2020-01-30

  The present invention provides compounds of formula (I) wherein all of the variables are as defined herein. These compounds are inhibitors of indoleamine 2,3-dioxygenase (IDO), which may be used as medicaments for the treatment of proliferative disorders, such as cancer, viral infections and/or autoimmune diseases.

  本发明提供了式（I）的化合物，其中所有变量如本文所定义。这些化合物是色氨酸2,3-二氧化酶（IDO）的抑制剂，可用作治疗增生性疾病，如癌症、病毒感染和/或自身免疫疾病的药物。
• (Chlorosulfonyl)benzenesulfonyl Fluorides—Versatile Building Blocks for Combinatorial Chemistry: Design, Synthesis and Evaluation of a Covalent Inhibitor Library
  作者：Kateryna A. Tolmachova、Yurii S. Moroz、Angelika Konovets、Maxim O. Platonov、Oleksandr V. Vasylchenko、Petro Borysko、Sergey Zozulya、Anastasia Gryniukova、Andrey V. Bogolubsky、Sergey Pipko、Pavel K. Mykhailiuk、Volodymyr S. Brovarets、Oleksandr O. Grygorenko

  DOI：10.1021/acscombsci.8b00130

  日期：2018.11.12

  Multigram synthesis of (chlorosulfonyl)benzenesulfonyl fluorides is described. Selective modification of these building blocks at the sulfonyl chloride function under parallel synthesis conditions is achieved. It is shown that the reaction scope includes the use of (hetero)aromatic and electron-poor aliphatic amines (e.g., amino nitriles). Utility of the method is demonstrated by preparation of the

  描述了（氯磺酰基）苯磺酰氟的多克合成。在平行合成条件下，实现了这些构件在磺酰氯官能团上的选择性修饰。结果表明，反应范围包括使用（杂）芳族和贫电子的脂族胺（例如氨基腈）。通过制备潜在用作共价片段的磺酰氟文库证明了该方法的实用性，这是通过计算机模拟和针对胰蛋白酶作为模型酶的体外筛选相结合来证明的。结果，鉴定了几种抑制剂，其活性与已知抑制剂相当。
• Substituted Phenylureas and Phenylamides as Vanilloid Receptor Ligands
  申请人：FRANK Robert

  公开号：US20120258946A1

  公开（公告）日：2012-10-11

  Substituted phenylureas and phenylamides, processes for their preparation, pharmaceutical compositions containing these compounds, and the use of these compounds for preparing pharmaceutical compositions.

  取代苯基脲和苯基酰胺，其制备过程，含有这些化合物的制药组合物以及使用这些化合物制备制药组合物的用途。
• IDO INHIBITORS
  申请人：Bristol-Myers Squibb Company

  公开号：US20160200674A1

  公开（公告）日：2016-07-14

  There are disclosed compounds that modulate or inhibit the enzymatic activity of indoleamine 2,3-dioxygenase (IDO), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders, such as cancer, viral infections and/or autoimmune diseases utilizing the compounds of the invention.

  本发明揭示了一些化合物，可调节或抑制吲哚胺2,3-二氧化酶（IDO）的酶活性，包括含有该化合物的制药组合物，以及利用本发明中的化合物治疗增生性疾病（如癌症、病毒感染和/或自身免疫疾病）的方法。