4-(2-fluoropropan-2-yl)benzenecarbonitrile | 1085453-68-4

• 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-(2-fluoropropan-2-yl)benzenecarbonitrile
• 英文别名: 4-(2-fluoropropan-2-yl)benzonitrile
• CAS: 1085453-68-4
• 化学式: C₁₀H₁₀FN
• 分子量: 163.195
• InChiKey: PDIMKSZACVVORK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  23.8
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-(2-fluoropropan-2-yl)benzenecarbonitrile 在 盐酸羟胺 、 三乙胺 作用下， 以 乙醇 为溶剂， 反应 1.0h， 以93%的产率得到4-(2-fluoropropan-2-yl)-N'-hydroxybenzenecarboximide amide
  参考文献：
  名称：

  WO2008/141731

  摘要：

  公开号：
• 作为产物：
  描述：

  4-(2-hydroxypropan-2-yl)benzonitrile 在 二乙胺基三氟化硫 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 以67%的产率得到4-(2-fluoropropan-2-yl)benzenecarbonitrile
  参考文献：
  名称：

  HETEROCYCLICALLY SUBSTITUTED ARYL COMPOUNDS AS HIF INHIBITORS

  摘要：

  本申请涉及具有杂环取代基的新型芳基化合物，其制备方法，它们用于治疗和/或预防疾病以及用于制备治疗和/或预防疾病的药物，特别是用于治疗和/或预防过度增殖和血管生成性疾病以及那些由于代谢适应缺氧状态而引起的疾病。这种治疗可以作为单独治疗进行，也可以与其他药物或进一步治疗措施结合使用。

  公开号：

  US20130196964A1

文献信息

• HETEROAROMATIC COMPOUNDS FOR USE AS HIF INHIBITORS
  申请人：Härter Michael

  公开号：US20110301122A1

  公开（公告）日：2011-12-08

  The present application relates to novel substituted aryl compounds, processes for their preparation, their use for treatment and/or prevention of diseases and their use for the preparation of medicaments for treatment and/or prevention of diseases, in particular for treatment and/or prevention of hyperproliferative and angiogenic diseases and those diseases which arise from metabolic adaptation to hypoxic states. Such treatments can be carried out as monotherapy or also in combination with other medicaments or further therapeutic measures.

  本申请涉及新型取代芳基化合物，其制备方法，它们用于治疗和/或预防疾病以及用于制备治疗和/或预防疾病的药物，特别是用于治疗和/或预防过度增殖和血管生成性疾病以及那些由于代谢适应缺氧状态而引起的疾病。这种治疗可以作为单独治疗进行，也可以与其他药物或进一步的治疗措施结合使用。
• Aryl compounds with aminoalkyl substituents and their use
  申请人：Härter Michael

  公开号：US20110312930A1

  公开（公告）日：2011-12-22

  The present application relates to novel aryl compounds with aminoalkyl substituents, to processes for their preparation, to their use for treatment and/or prevention of diseases and to their use for the preparation of medicaments for treatment and/or prevention of diseases, in particular for treatment and/or prevention of hyperproliferative and angiogenic diseases and those diseases which arise from metabolic adaptation to hypoxic states. Such treatments can be carried out as monotherapy or also in combination with other medicaments or further therapeutic measures.

  本申请涉及具有氨基烷基取代基的新型芳基化合物，涉及其制备方法，涉及它们用于治疗和/或预防疾病以及用于制备治疗和/或预防疾病的药物的用途，特别是用于治疗和/或预防过度增殖和血管生成性疾病以及那些由于代谢适应低氧状态而引起的疾病。这种治疗可以作为单独治疗进行，也可以与其他药物或进一步的治疗措施结合使用。
• HETEROARYL SUBSTITUTED PYRAZOLE DERIVATIVES USEFUL FOR TREATING HYPER-PROLIFERATIVE DISORDERS AND DISEASES ASSOCIATED WITH ANGIOGENESIS
  申请人：Boyer Stephen

  公开号：US20100249085A1

  公开（公告）日：2010-09-30

  This invention relates to novel heteroaryl substituted pyrazole compounds, pharmaceutical compositions containing such compounds and the use of those compounds or compositions for treating hyper-proliferative and/or angiogenesis disorders, as a sole agent or in combination with other active ingredients or therapeutic measures.

  本发明涉及新型杂环取代吡唑化合物、含有这些化合物的药物组合物以及用于治疗过度增殖和/或血管生成障碍的这些化合物或组合物的用途，作为单一药物或与其他活性成分或治疗措施联合使用。
• Heteroaryl substituted pyrazole derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis
  申请人：Boyer Stephen

  公开号：US08796253B2

  公开（公告）日：2014-08-05

  This invention relates to novel heteroaryl substituted pyrazole compounds, pharmaceutical compositions containing such compounds and the use of those compounds or compositions for treating hyper-proliferative and/or angiogenesis disorders, as a sole agent or in combination with other active ingredients or therapeutic measures.

  本发明涉及新型杂环取代吡唑化合物、含有这些化合物的药物组合物以及将这些化合物或组合物用于治疗过度增殖和/或血管生成障碍的方法，作为单一药物或与其他活性成分或治疗措施联合使用。
• Chemo‐ and Site‐Selective Electro‐Oxidative Alkane Fluorination by C(sp ³ )−H Cleavage
  作者：Maximilian Stangier、Alexej Scheremetjew、Lutz Ackermann

  DOI：10.1002/chem.202201654

  日期：2022.10.26

  AbstractElectrochemical fluorinations of C(sp3)−H bonds with a nucleophilic fluoride source have been accomplished in a chemo‐ and site‐selective fashion, avoiding the use of electrophilic F+ sources and stoichiometric oxidants. The introduced metal‐free strategy exhibits high functional group tolerance, setting the stage for late‐stage fluorinations of biorelevant motifs. The synthetic utility of the C(sp3)−H fluorination was reflected by subsequent one‐pot arylation of the generated benzylic fluorides.