2,4,5-trichloro-6-(2,6-dibromo-4-(trifluoromethoxy)phenylamino)isophthalonitrile | 1416419-97-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 2,4,5-trichloro-6-(2,6-dibromo-4-(trifluoromethoxy)phenylamino)isophthalonitrile
• 英文别名: 2,4,5-Trichloro-6-[2,6-dibromo-4-(trifluoromethoxy)anilino]benzene-1,3-dicarbonitrile；2,4,5-trichloro-6-[2,6-dibromo-4-(trifluoromethoxy)anilino]benzene-1,3-dicarbonitrile
• CAS: 1416419-97-0
• 化学式: C₁₅H₃Br₂Cl₃F₃N₃O
• 分子量: 564.371
• InChiKey: DLFBLTDFEHNPIE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.9
• 重原子数：
  27
• 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：
  68.8
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  2,4,5-trichloro-6-(4-(trifluoromethoxy)phenylamino)isophthalonitrile 在 N-溴代丁二酰亚胺(NBS) 、 过氧化苯甲酰 作用下， 以 四氯化碳 为溶剂， 反应 5.0h， 以69%的产率得到2,4,5-trichloro-6-(2,6-dibromo-4-(trifluoromethoxy)phenylamino)isophthalonitrile
  参考文献：
  名称：

  Synthesis and fungicidal activity of fluorine-containing chlorothalonil derivatives

  摘要：

  Fourteen new fluorine-containing chlorothalonil derivatives were synthesized by using intermediate derivatization method (IDM) in order to discover novel antifungal compounds for controlling corn rust. The structures of synthesized compounds were confirmed by H-1 NMR, C-13 NMR, F-19 NMR, elemental analysis, HRMS and X-ray. The bioassay results indicated that compound 2,4,5-trichloro-6-(2,6-dichloro-4-[trifluoromethyl]phenylamino)isophthalonitrile (3j, R-n is 2,6-Cl2-4-CF3) had the optimal structure with best fungicidal activity against corn rust (98%, 70% controls) at 25 and 6.25 mg/L concentration, respectively, much better than chlorothalonil and fluazinam, highlighting the importance of trifluoromethyl group on 4-position of benzene ring. The structure-activity relationship of the synthesized compounds was discussed as well. (C) 2014 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jfluchem.2014.01.006

文献信息

• SUBSTITUTE DIPHENYLAMINE COMPOUNDS USE THEREOF AS ANTITUMOR AGENTS
  申请人：SINOCHEM CORPORATION

  公开号：US20150011628A1

  公开（公告）日：2015-01-08

  The invention relates to substituted diphenylamine compounds using as antitumor agents. The structure of the compounds is represented as the general formula (I): The groups are as defined as specification. The compound represented by formula (I) showed potent antitumor activity, especially to cure or alleviate the cancer causing by cancer cells of human tissue or organ. The preferred cancers are: colon cancer, liver cancer, lymph cancer, lung cancer, esophageal cancer, breast cancer, central nervous system cancer, melanoma, ovarian cancer, cervical cancer, renal cancer, leukemia, prostatic cancer, pancreatic cancer, bladder cancer, rectal cancer, osteosarcoma, nasopharynx cancer or stomach cancer.

  该发明涉及以取代二苯胺化合物作为抗肿瘤药剂。化合物的结构表示为通式(I)：其中各个基团如规范所定义。由通式(I)表示的化合物显示出强效的抗肿瘤活性，特别是用于治疗或缓解由人体组织或器官的癌细胞引起的癌症。首选的癌症包括：结肠癌、肝癌、淋巴癌、肺癌、食管癌、乳腺癌、中枢神经系统癌、黑色素瘤、卵巢癌、宫颈癌、肾癌、白血病、前列腺癌、胰腺癌、膀胱癌、直肠癌、骨肉瘤、鼻咽癌或胃癌。
• Design, Synthesis, and Structure–Activity Relationship of Novel Aniline Derivatives of Chlorothalonil
  作者：Ai-Ying Guan、Chang-Ling Liu、Guang Huang、Hui-Chao Li、Shu-Lin Hao、Ying Xu、Zhi-Nian Li

  DOI：10.1021/jf403739e

  日期：2013.12.11

  chlorine groups in the phenyl ring in phenyl amine with other functional groups. These functional groups with various electronic properties and spatial characteristics were considered to explore the relationship between structure and fungicidal activity. The results indicate that the electron-withdrawing group NO2 on the 4 position on the right phenyl ring plays a unique role on enhancing the fungicidal

  具有低成本和低毒性的氯噻酮是在农业化学领域中广泛使用的杀真菌剂。该化合物上亲核基团的存在允许进一步的化学修饰以获得新的百菌清衍生物。另一种具有广谱杀真菌谱的可商购药物Fluazinam具有二芳基胺结构的支架。为了模拟该主链结构，使用多种（未）取代的苯胺作为亲核试剂与百菌清进行反应，从而获得具有二苯胺结构的化合物。通过优雅的设计，形成了两个引线2,4,5-三氯-6-（2,4-二氯苯基氨基）间苯二甲腈（7）和2,4,5-三氯-6-（2,4,6-三氯苯基氨基）间苯二甲腈（11），经过初步的生物测定筛选后发现具有潜在的杀真菌活性。通过将苯胺中苯环中的氯基团替换为其他官能团，进一步修饰了这两种铅，以获得最终产物。这些具有各种电子特性和空间特征的官能团被认为是探索结构与杀真菌活性之间的关系。结果表明，吸电子基团NO 2在右苯环的4位上的化合物在增强杀真菌活性方面起着独特的作用。通过质子核磁共振和元素分
• USE OF SUBSTITUTED DIPHENYLAMINE COMPOUNDS IN PREPARING ANTI-TUMOUR DRUGS
  申请人：Sinochem Corporation

  公开号：EP2826474B1

  公开（公告）日：2021-05-26
• US9376376B2
  申请人：——

  公开号：US9376376B2

  公开（公告）日：2016-06-28
• Synthesis and fungicidal activity of fluorine-containing chlorothalonil derivatives
  作者：Aiying Guan、Changling Liu、Guang Huang、Huichao Li、Shulin Hao、Ying Xu、Yong Xie、Zhinian Li

  DOI：10.1016/j.jfluchem.2014.01.006

  日期：2014.4

  Fourteen new fluorine-containing chlorothalonil derivatives were synthesized by using intermediate derivatization method (IDM) in order to discover novel antifungal compounds for controlling corn rust. The structures of synthesized compounds were confirmed by H-1 NMR, C-13 NMR, F-19 NMR, elemental analysis, HRMS and X-ray. The bioassay results indicated that compound 2,4,5-trichloro-6-(2,6-dichloro-4-[trifluoromethyl]phenylamino)isophthalonitrile (3j, R-n is 2,6-Cl2-4-CF3) had the optimal structure with best fungicidal activity against corn rust (98%, 70% controls) at 25 and 6.25 mg/L concentration, respectively, much better than chlorothalonil and fluazinam, highlighting the importance of trifluoromethyl group on 4-position of benzene ring. The structure-activity relationship of the synthesized compounds was discussed as well. (C) 2014 Elsevier B.V. All rights reserved.