3-(3-氯-苯氧基)-苯胺 | 105945-23-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-(3-氯-苯氧基)-苯胺
• 英文名称: 3-(3-chloro-phenoxy)-aniline
• 英文别名: 3-(3-Chlor-phenoxy)-anilin；3-(3-Chlorophenoxy)aniline
• CAS: 105945-23-1
• 化学式: C₁₂H₁₀ClNO
• 分子量: 219.671
• InChiKey: UJIZWPQGPAULGD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  35.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-氯-4-甲氧基嘧啶 、 3-(3-氯-苯氧基)-苯胺 在 对甲苯磺酸 作用下， 以 1,4-二氧六环 为溶剂， 反应 5.0h， 生成 N-[3-(3-chlorophenoxy)phenyl]-4-methoxy-pyrimidin-2-amine
  参考文献：
  名称：

  Efficient Discovery of Potent Anti-HIV Agents Targeting the Tyr181Cys Variant of HIV Reverse Transcriptase

  摘要：

  Non-nucleoside reverse transcriptase inhibitors (NNRTIs) that interfere with the replication of human immunodeficiency virus (HIV) are being pursued with guidance from molecular modeling including free-energy perturbation (FEP) calculations for protein inhibitor binding affinities. The previously reported pyrimidinylphenylamine 1 and its chloro analogue 2 are potent anti-HIV agents; they inhibit replication of wild-type HIV-1 in infected human T-cells with EC50 values of 2 and 10 nM, respectively. However, they show no activity against viral strains containing the Tyr181Cys (Y181C) mutation in HIV-RT. Modeling indicates that the problem is likely associated with extensive interaction between the dimethylallyloxy substituent and Tyr181. As an alternative, a phenoxy group is computed to be oriented in a manner diminishing the contact with Tyr181. However, this replacement leads to a roughly 1000-fold loss of activity for 3 (2.5 mu M). The present report details the efficient, computationally driven evolution of 3 to novel NNRTIs with sub-10 nM potency toward both wild-type HIV-1 and Y181C-containing variants. The critical contributors were FEP substituent scans for the phenoxy and pyrimidine rings and recognition of potential benefits of addition of a cyanovinyl group to the phenoxy ring.

  DOI：

  10.1021/ja2058583
• 作为产物：
  描述：

  间溴硝基苯 在 氢氧化钾 、 铜 、 一水合肼 作用下， 反应 2.0h， 生成 3-(3-氯-苯氧基)-苯胺
  参考文献：
  名称：

  Ikawa, Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1959, vol. 79, p. 273,275

  摘要：

  DOI：

文献信息

• Ketones
  申请人：Barton John Peter

  公开号：US20050272036A1

  公开（公告）日：2005-12-08

  Compounds of formula (I): wherein variable groups are as defined within; for use in the inhibition of 11βHSD1 are described.

  描述了式(I)的化合物：其中变量基团如定义的那样；用于抑制11βHSD1。
• AMINOMETHYL-4-IMIDAZOLES
  申请人：Galley Guido

  公开号：US20080119535A1

  公开（公告）日：2008-05-22

  The present invention relates to amino-4-methyl imidazoles and pharmaceutically-acceptable salts thereof. The compound may be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders such as schizophrenia, neurological diseases such as Parkinson's disease, neurodegenerative disorders such as Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse and metabolic disorders such as eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.

  本发明涉及氨基-4-甲基咪唑及其药学可接受的盐。该化合物可用于治疗抑郁症、焦虑症、双相障碍、注意力缺陷多动障碍（ADHD）、压力相关障碍、精神病性障碍如精神分裂症、神经系统疾病如帕金森病、神经退行性疾病如阿尔茨海默病、癫痫、偏头痛、高血压、物质滥用和代谢性疾病如进食障碍、糖尿病、糖尿病并发症、肥胖症、脂质代谢异常、能量消耗和吸收障碍、体温稳态的障碍和功能障碍、睡眠和昼夜节律障碍以及心血管疾病的治疗。
• Fungicidal heterocyclic aromatic amides, their compositions and methods of use
  申请人：Dow AgroSciences LLC

  公开号：EP1493733A2

  公开（公告）日：2005-01-05

  The present invention relates to the field of fungicidal compositions and methods. More particularly, the present invention concerns novel fungicidal heterocyclic aromatic amides of following formula I: wherein: represents a 5 membered heterocyclic aromatic ring, and methods involving application of fungicidally effective amounts of such compounds to the locus of a plant pathogen. The present invention also concerns methods useful in the preparation of heterocyclic aromatic amides and their fungicidal compositions.

  本发明涉及杀菌组合物和方法领域。更具体地说，本发明涉及下式 I 的新型杀菌杂环芳香酰胺： 其中 代表 5 个成员的杂环芳香环，以及将杀真菌有效量的此类化合物施用到植物病原体位点的方法。本发明还涉及用于制备杂环芳香酰胺及其杀菌组合物的方法。
• Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation
  申请人：Dow AgroSciences, LLC

  公开号：EP1516874B1

  公开（公告）日：2015-08-19
• CH557804
  申请人：——

  公开号：——

  公开（公告）日：——