4-(3-phenylpropoxy)benzonitrile | 18859-07-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 4-(3-phenylpropoxy)benzonitrile
• CAS: 18859-07-9
• 化学式: C₁₆H₁₅NO
• mdl: MFCD09718491
• 分子量: 237.301
• InChiKey: OWLIMDVGNCFIIC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.187
• 拓扑面积：
  33
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-(3-phenylpropoxy)benzonitrile 以43%的产率得到
  参考文献：
  名称：

  WAGNER G.; HORN H., PHARMAZIE , 1975, 30, NO 6, 353-357

  摘要：

  DOI：
• 作为产物：
  描述：

  3-苯丙醇 、 对氟苯腈 在 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 生成 4-(3-phenylpropoxy)benzonitrile
  参考文献：
  名称：

  [EN] INHIBITORS OF SPINSTER HOMOLOG 2 (SPNS2) FOR USE IN THERAPY
  [FR] INHIBITEURS DE L'HOMOLOGUE 2 DE SPINSTER (SPNS2) DESTINÉS À ÊTRE UTILISÉS EN THÉRAPIE

  摘要：

  本公开提供了根据公式I提供的SPNS2抑制剂化合物及其药学上可接受的盐，以及/或在公开中描述的互变异构体，并且公开提供了它们的药物组合物以及在治疗中使用的方法。

  公开号：

  WO2020154431A1

文献信息

• Activation of Remote <i>meta</i> -C−H Bonds in Arenes with Tethered Alcohols: A Salicylonitrile Template
  作者：Lanlan Zhang、Chaoyue Zhao、Yang Liu、Jiancong Xu、Xiufang Xu、Zhong Jin

  DOI：10.1002/anie.201705495

  日期：2017.9.25

  Palladium‐catalyzed activation of remote meta‐C−H bonds in arenes containing tethered alcohols was achieved with high regioselectivity by using a nitrile template. Computational studies on the macrocyclic transition state of the regioselectivity‐determining C−H activation steps revealed that both the C‐N‐Ag angles and gauche comformations of phenyl ether play an extremely important role in the meta selectivity

  通过使用腈模板，在具有区域选择性的情况下，钯催化了含拴链醇的芳烃中偏碳氢键的活化。上的区域选择性决定C-H活化步骤的大环过渡态的计算研究显示，无论是C-N-银角和苯基的笨拙comformations醚起到极其重要的作用的元 的选择性。
• 1,2,4-oxadiazole derivatives having monoamine oxidase B
  申请人：Wakamoto Pharmaceutical Co., Ltd.

  公开号：US05356916A1

  公开（公告）日：1994-10-18

  A 1,2,4-oxadiazole derivative is represented by the following general formula (I): ##STR1## wherein R.sup.1 represents a lower alkyl or cycloalkyl group, a lower alkyl group substituted with a halogen atom, a lower alkylamino group or a phenyl group; R.sup.2 represents a hydrogen atom, a lower dialkylamino group, a cyclic alkylamino group, a cyclic amino group having an oxygen or nitrogen atom in the ring, a phenyl group which may be substituted with a halogen atom, a pyridyl group, an imidazolyl group, an alkylimidazolyl group, a benzimidazolyl group or a 2-oxopyrrolidinyl group; and n is 1, 2 or 3. The derivative has excellent monoamine oxidase-inhibitory activity and is effective as a medicine for treating Parkinson's disease.

  一种1,2,4-噁二唑衍生物的通式(I)如下：##STR1##其中，R1代表低碳基或环烷基、低碳基取代的卤素基、低碳基氨基或苯基；R2代表氢原子、低二烷基氨基基团、环烷氨基基团、环氧原子或氮原子在环中的环氨基基团、苯基（可取代卤素原子）、吡啶基、咪唑基、烷基咪唑基、苯并咪唑基或2-氧代吡咯烷基；n为1、2或3。该衍生物具有出色的单胺氧化酶抑制活性，是治疗帕金森病的有效药物。
• Room-Temperature, Transition-Metal-Free Arylation of Alcohols with Aryl Bromides
  作者：Yanqing Wang、David J. Young、Hong-Xi Li、Da-Liang Zhu、Jie Li、Qi Wu

  DOI：10.1055/a-1932-6146

  日期：2023.2

  Sodium tert-butoxide promotes the efficient etherification of alcohols with aryl bromides at room temperature. This simple procedure has a broad substrate scope, providing a practical pathway to aryl alkyl ethers in good yields without the addition of any transition metal species.

  叔丁醇钠促进醇与芳基溴在室温下的有效醚化。这种简单的过程具有广泛的底物范围，为在不添加任何过渡金属物质的情况下以高收率制备芳基烷基醚提供了一条实用途径。
• Design and optimization of hybrid of 2,4-diaminopyrimidine and arylthiazole scaffold as anticancer cell proliferation and migration agents
  作者：Wenbo Zhou、Anling Huang、Yong Zhang、Qingxiang Lin、Weikai Guo、Zihua You、Zhengfang Yi、Mingyao Liu、Yihua Chen

  DOI：10.1016/j.ejmech.2015.04.027

  日期：2015.5

  Therapeutics of metastatic or triple-negative breast cancer are still challenging in clinical. Herein we demonstrated the design and optimization of a series of hybrid of 2,4-diaminopyrimidine and arylthiazole derivatives for their anti-proliferative properties against two breast cancer cell lines (MCF-7 as human breast cancer and MDA-MB-231 as triple-negative breast cancer). More importantly, some of those compounds with potent antiproliferative activities also indicated excellent inhibitory activities against MDA-MB-231 cell migration. These results suggested that the new series of hybridation of arylthiazoles and aminopyrimidines could be identified and developed as novel highly potential anticancer agents against the triple-negative breast cancer as well as metastatic one in the future. (C) 2015 Elsevier Masson SAS. All rights reserved.
• 1,2,4-Oxadiazole derivatives having monoamine oxidase B enzyme-inhibitory activity and method for preparing same
  申请人：Wakamoto Pharmaceutical Co., Ltd.

  公开号：EP0504574B1

  公开（公告）日：1996-02-28