8-methyl-2,3-diphenyl-4H-chromen-4-one

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 异黄酮类化合物
• 英文名称: 8-methyl-2,3-diphenyl-4H-chromen-4-one
• 英文别名: 8-Methyl-2,3-diphenylchromen-4-one
• 化学式: C₂₂H₁₆O₂
• 分子量: 312.368
• InChiKey: PXKQLYHUYHWHGJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  24
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  8-methyl-2,3-diphenyl-4H-chromen-4-one 在 N-溴代丁二酰亚胺(NBS) 、 偶氮二异丁腈 作用下， 以 四氯化碳 、 二氯甲烷 为溶剂， 反应 7.0h， 生成 2-(4-oxo-2,3-diphenyl-4H-chromen-8-yl)acetonitrile
  参考文献：
  名称：

  Synthesis and anticancer activities of 3-arylflavone-8-acetic acid derivatives

  摘要：

  This paper describes the synthesis and the antiproliferative activities of compounds 9a-r, 3-aryl analogs of flavone-8-acetic acid that bear diverse substituents on the benzene rings at the 2- and 3-positions of the flavone nucleus. Their direct and indirect cytotoxicities were evaluated against HT-29 human colon adenocarcinoma cell lines, A549 lung adenocarcinoma cell lines and Human Peripheral Blood Mononuclear Cells (HPBMCs). The results indicate that most of the compounds bearing electron-withdrawing substituents (9b-m) exhibited moderate direct cytotoxicities. And compounds 9e and 9i showed comparable indirect cytotoxicities with 5, 6-dimethylxanthenone-4-acetic acid (DMXAA), and low direct cytotoxicities toward HPBMCs. Interestingly, the compounds 9n-r bearing methoxy groups at the 2- or 3-position of the flavone nucleus exhibited higher indirect cytotoxicities against A549 cell lines than DMXAA, and lower cytotoxicities against HPBMCs. In addition, compounds 9p-r were found to be able to induce tumor necrosis factor alpha (TNF-alpha) production in HPBMCs. (C) 2014 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2014.11.030
• 作为产物：
  描述：

  1-(2-羟基-3-甲基苯基)-2-苯基乙酮 在 吡啶 作用下， 以 甘油 为溶剂， 反应 7.0h， 生成 8-methyl-2,3-diphenyl-4H-chromen-4-one
  参考文献：
  名称：

  Synthesis and anticancer activities of 3-arylflavone-8-acetic acid derivatives

  摘要：

  This paper describes the synthesis and the antiproliferative activities of compounds 9a-r, 3-aryl analogs of flavone-8-acetic acid that bear diverse substituents on the benzene rings at the 2- and 3-positions of the flavone nucleus. Their direct and indirect cytotoxicities were evaluated against HT-29 human colon adenocarcinoma cell lines, A549 lung adenocarcinoma cell lines and Human Peripheral Blood Mononuclear Cells (HPBMCs). The results indicate that most of the compounds bearing electron-withdrawing substituents (9b-m) exhibited moderate direct cytotoxicities. And compounds 9e and 9i showed comparable indirect cytotoxicities with 5, 6-dimethylxanthenone-4-acetic acid (DMXAA), and low direct cytotoxicities toward HPBMCs. Interestingly, the compounds 9n-r bearing methoxy groups at the 2- or 3-position of the flavone nucleus exhibited higher indirect cytotoxicities against A549 cell lines than DMXAA, and lower cytotoxicities against HPBMCs. In addition, compounds 9p-r were found to be able to induce tumor necrosis factor alpha (TNF-alpha) production in HPBMCs. (C) 2014 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2014.11.030

文献信息

• Iridium-Catalyzed and Ligand-Controlled Carbonylative Synthesis of Flavones from Simple Phenols and Internal Alkynes
  作者：Fengxiang Zhu、Zechao Wang、Yahui Li、Xiao-Feng Wu

  DOI：10.1002/chem.201700233

  日期：2017.3.8

  Flavones are important natural products with diverse biological activities. In this study, a novel procedure for the carbonylative synthesis of flavones has been developed by using simple phenols and internal alkynes as the substrates. Various flavones were isolated in moderate to good yields with excellent regioselectivity and functional group tolerance by using an iridium catalyst system. Notably

  黄酮是具有多种生物活性的重要天然产物。在这项研究中，通过使用简单的苯酚和内部炔烃作为底物，开发了一种黄酮羰基合成的新方法。通过使用铱催化剂体系，以中度到良好的收率分离出各种黄酮，具有出色的区域选择性和官能团耐受性。值得注意的是，这是直接将未预活化的苯酚和炔烃进行羰基环化以生成黄酮的例子，而配体的选择对这种转化的成功至关重要。
• Palladium-Catalyzed Carbonylative Synthesis of 2,3-Disubstituted Chromones
  作者：Chaoren Shen、Wanfang Li、Hongfei Yin、Anke Spannenberg、Troels Skrydstrup、Xiao-Feng Wu

  DOI：10.1002/adsc.201500858

  日期：2016.2.4

  An unexpected palladium‐catalyzed carbonylative synthesis of 2,3‐disubstituted chromones has been developed. Starting from 2‐bromofluorobenzenes and ketones, the corresponding chromones were produced in good yields. By control experiments, this transformation was found to proceed through a sequential carbonylation/Claisen–Hasse rearrangement/intramolecular nucleophilic aromatic substitution approach

  已经开发出了出乎意料的钯催化的2,3-二取代色酮的羰基合成。从2-溴氟苯和酮开始，以高收率生产了相应的色酮。由对照实验中，这种转变被发现通过连续的羰基化/克莱森-哈斯重排/分子内的亲核芳香取代的方法（S进行Ñ AR）。更具体地说，反应顺序始于酮与邻溴氟苯的钯催化羰基化反应，得到乙烯基苯甲酸酯，随后通过克莱森-哈斯重排将其转化为1,3-二酮。最终产物的分子内年代后产生Ñ的氩反应原位形成1,3-二酮。
• Nickel-catalyzed C–O/O–H Annulation of Salicylate Esters with Alkynes: Activation of C–O Bond in Esters
  作者：Yasuaki Iyori、Naoto Chatani

  DOI：10.1246/cl.200885

  日期：2021.3.5

  The Ni-catalyzed C−O/O−H annulation of salicylate esters with alkynes, leading to the production of chromone derivatives is reported. The key step in the reaction is the cleavage of an acyl C-O bond. The presence of a base is essential for the reaction to proceed.

  据报道，Ni催化水杨酸酯与炔烃的C-O / O-H环化反应，导致色酮衍生物的产生。反应中的关键步骤是裂解酰基CO键。碱的存在对于反应进行是必不可少的。
• Synthesis and anticancer activities of 3-arylflavone-8-acetic acid derivatives
  作者：Guang-Hua Yan、Xiao-Fang Li、Bing-Chen Ge、Xiu-Dong Shi、Yu-Fang Chen、Xue-Mei Yang、Jiang-Ping Xu、Shu-Wen Liu、Pei-Liang Zhao、Zhong-Zhen Zhou、Chun-Qiong Zhou、Wen-Hua Chen

  DOI：10.1016/j.ejmech.2014.11.030

  日期：2015.1

  This paper describes the synthesis and the antiproliferative activities of compounds 9a-r, 3-aryl analogs of flavone-8-acetic acid that bear diverse substituents on the benzene rings at the 2- and 3-positions of the flavone nucleus. Their direct and indirect cytotoxicities were evaluated against HT-29 human colon adenocarcinoma cell lines, A549 lung adenocarcinoma cell lines and Human Peripheral Blood Mononuclear Cells (HPBMCs). The results indicate that most of the compounds bearing electron-withdrawing substituents (9b-m) exhibited moderate direct cytotoxicities. And compounds 9e and 9i showed comparable indirect cytotoxicities with 5, 6-dimethylxanthenone-4-acetic acid (DMXAA), and low direct cytotoxicities toward HPBMCs. Interestingly, the compounds 9n-r bearing methoxy groups at the 2- or 3-position of the flavone nucleus exhibited higher indirect cytotoxicities against A549 cell lines than DMXAA, and lower cytotoxicities against HPBMCs. In addition, compounds 9p-r were found to be able to induce tumor necrosis factor alpha (TNF-alpha) production in HPBMCs. (C) 2014 Elsevier Masson SAS. All rights reserved.