3-chloro-5-(5-chloro-2-methoxybenzoyl)benzonitrile | 329944-63-0

• 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: 3-chloro-5-(5-chloro-2-methoxybenzoyl)benzonitrile
• CAS: 329944-63-0
• 化学式: C₁₅H₉Cl₂NO₂
• 分子量: 306.148
• InChiKey: AOBVGWHEOIZDMM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  50.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-chloro-5-(5-chloro-2-methoxybenzoyl)benzonitrile 在 三溴化硼 、 potassium carbonate 作用下， 以 二氯甲烷 、 丙酮 为溶剂， 反应 6.41h， 生成 Ethyl 2-[4-chloro-2-(3-chloro-5-cyanobenzoyl)phenoxy]acetate
  参考文献：
  名称：

  Structure−Activity Relationship Studies of Novel Benzophenones Leading to the Discovery of a Potent, Next Generation HIV Nonnucleoside Reverse Transcriptase Inhibitor

  摘要：

  Despite the progress of the past two decades, there is still considerable need for safe, efficacious drugs that target human immunodeficiency virus (HIV). This is particularly true for the growing number of patients infected with virus resistant to currently approved HIV drugs. Our high throughput screening effort identified a benzophenone template as a potential nonnucleoside reverse transcriptase inhibitor (NNRTI). This manuscript describes our extensive exploration of the benzophenone structure-activity relationships, which culminated in the identification of several compounds with very potent inhibition of both wild type and clinically relevant NNRTI-resistant mutant strains of HIV. These potent inhibitors include 70h (GW678248), which has in vitro antiviral assay IC50 values of 0.5 nM against wild-type HIV, 1 nM against the K103N mutant associated with clinical resistance to efavirenz, and 0.7 nM against the Y181C mutant associated with clinical resistance to nevirapine. Compound 70h has also demonstrated relatively low clearance in intravenous pharmacokinetic studies in three species, and it is the active component of a drug candidate which has progressed to phase 2 clinical studies.

  DOI：

  10.1021/jm050670l
• 作为产物：
  描述：

  5-氯-2-甲氧基苯甲酸 在 copper(l) iodide 、 四(三苯基膦)钯 、 正丁基锂 、 草酰氯 、 三乙胺 、 N,N-二甲基甲酰胺 作用下， 以 乙醚 、 正己烷 、 二氯甲烷 、 氯仿 、 乙腈 为溶剂， 反应 39.67h， 生成 3-chloro-5-(5-chloro-2-methoxybenzoyl)benzonitrile
  参考文献：
  名称：

  Structure−Activity Relationship Studies of Novel Benzophenones Leading to the Discovery of a Potent, Next Generation HIV Nonnucleoside Reverse Transcriptase Inhibitor

  摘要：

  Despite the progress of the past two decades, there is still considerable need for safe, efficacious drugs that target human immunodeficiency virus (HIV). This is particularly true for the growing number of patients infected with virus resistant to currently approved HIV drugs. Our high throughput screening effort identified a benzophenone template as a potential nonnucleoside reverse transcriptase inhibitor (NNRTI). This manuscript describes our extensive exploration of the benzophenone structure-activity relationships, which culminated in the identification of several compounds with very potent inhibition of both wild type and clinically relevant NNRTI-resistant mutant strains of HIV. These potent inhibitors include 70h (GW678248), which has in vitro antiviral assay IC50 values of 0.5 nM against wild-type HIV, 1 nM against the K103N mutant associated with clinical resistance to efavirenz, and 0.7 nM against the Y181C mutant associated with clinical resistance to nevirapine. Compound 70h has also demonstrated relatively low clearance in intravenous pharmacokinetic studies in three species, and it is the active component of a drug candidate which has progressed to phase 2 clinical studies.

  DOI：

  10.1021/jm050670l

文献信息

• Synthesis of Functionalized Ketones from Acid Chlorides and Organolithiums by Extremely Fast Micromixing
  作者：Aiichiro Nagaki、Kengo Sasatsuki、Satoshi Ishiuchi、Nobuyuki Miuchi、Masahiro Takumi、Jun‐ichi Yoshida

  DOI：10.1002/chem.201900743

  日期：2019.4

  Synthesis of ketones containing various functional groups from acid chlorides bearing electrophilic functional groups and functionalized organolithiums was achieved using a flow microreactor system. Extremely fast mixing is important for high chemoselectivity.

  使用流动微反应器系统，可以从带有亲电官能团的酰基氯和官能化的有机锂合成含各种官能团的酮。极快的混合对于高化学选择性很重要。
• Visible light-driven direct synthesis of ketones from aldehydes via C H bond activation using NiCu nanoparticles adorned on carbon nano onions
  作者：Zahra Khorsandi、S. Fatemeh Mohammadi Metkazini、Akbar Heydari、Rajender S. Varma

  DOI：10.1016/j.mcat.2021.111987

  日期：2021.11

  An efficient, straightforward and high yield synthetic approach is described for the direct synthesis of diaryl ketones via the CH bond activation of aldehydes using NiCu nanoparticles adorned on carbon nano onions as an efficient heterogeneous catalyst under the irradiation of a mercury-vapor lamp (400 w) via simple workup. This CH bond activation reaction appears simple and convenient with a wide

  描述了一种高效、直接和高收率的合成方法，用于通过醛的 CH键活化直接合成二芳基酮，使用装饰在碳纳米洋葱上的 NiCu 纳米粒子作为高效的多相催化剂，在汞蒸气灯 (400 w) 通过简单的检查。这种C H键活化反应因其优异的合成能力而显得简单方便，底物范围广，如在更绿色温和的反应条件下制备新批准的抗阿尔茨海默病和抗HIV药物化合物所示；催化剂可以循环使用5次，催化活性没有任何损失。
• Benzophenones as inhibitors of reverse transcriptase
  申请人：SmithKline Beecham Corporation

  公开号：US06995283B2

  公开（公告）日：2006-02-07

  The present invention is directed to beazophenone compounds useful in the inhibition of HIV reverse transcriptase, particularly its resistant varieties.

  本发明涉及苯并酮化合物，其在抑制HIV逆转录酶方面具有用处，特别是在抑制其耐药品种方面。
• WO2007/121415
  申请人：——

  公开号：——

  公开（公告）日：——
• BENZOPHENONES AS INHIBITORS OF REVERSE TRANSCRIPTASE
  申请人：GLAXO GROUP LIMITED

  公开号：EP1208091B1

  公开（公告）日：2006-05-03