(4-chlorophenyl)(2-(4-chlorophenyl)-1H-indol-3-yl)methanone | 1330540-15-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: (4-chlorophenyl)(2-(4-chlorophenyl)-1H-indol-3-yl)methanone
• 英文别名: (4-chlorophenyl)-[2-(4-chlorophenyl)-1H-indol-3-yl]methanone
• CAS: 1330540-15-2
• 化学式: C₂₁H₁₃Cl₂NO
• 分子量: 366.246
• InChiKey: JFOQHOOKGZPPQP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.3
• 重原子数：
  25
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  32.9
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  对氯苯乙酮 在 甲烷磺酸 作用下， 生成 (4-chlorophenyl)(2-(4-chlorophenyl)-1H-indol-3-yl)methanone
  参考文献：
  名称：

  Unprecedented C-2 arylation of indole with diazonium salts: Syntheses of 2,3-disubstituted indoles and their antimicrobial activity

  摘要：

  A novel reaction of indole with aryldiazonium salts leading to the formation of 2-aryl-3-(arylazo)indoles was discovered. The products were found to possess potent anti-MRSA and anti-LLVRE activities. The SAR studies indicate that the potentially metabolically labile azo functionality can be replaced with ether oxygen and thioether sulfur atoms without any loss of activity. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.06.081

文献信息

• Antibiotic sensitivity-restoring and photosensitive agents
  申请人：NEW MEXICO TECH UNIVERSITY RESEARCH PARK CORPORATION

  公开号：US10239834B2

  公开（公告）日：2019-03-26

  The present disclosure describes a method to treat conditions, including bacterial infections and cancer, using a photosensitive compound that, upon exposure to white light, can be activated. The photosensitive compound can also interact synergistically with antibiotics used concomitantly to kill drug-resistant bacteria. The photosensitive compounds can also be used to inhibit the proliferation of cancer cells.

  本公开描述了一种使用光敏化合物治疗细菌感染和癌症等疾病的方法，该化合物在白光照射下可被激活。光敏化合物还能与同时使用的抗生素产生协同作用，杀死耐药细菌。光敏化合物还可用于抑制癌细胞的增殖。
• α-Hydroxydimethylacetal/ketal as an α-hydroxycarbonyl equivalent in interrupted Heyns/Amadori rearrangement: regioselective synthesis of substituted C2- and C3-acylindoles
  作者：Minakshi Altia、Pazhamalai Anbarasan

  DOI：10.1039/d4nj00771a

  日期：——

  intramolecular trapping of the aminoenol intermediate derived from o-acyl/formylanilines and α-hydroxydimethylacetals/ketals followed by rearrangement/aromatization in the presence of acid. Important features include the use of α-hydroxydimethylacetal/ketal as an α-hydroxycarbonyl equivalent, excellent regiocontrol, good functional group tolerance, selective synthesis of acylindoles, gram-scale synthesis, and

  海恩斯/阿马多里重排允许通过生成氨基烯醇中间体，从 α-羟基羰基和胺合成 α-氨基羰基化合物。在目前的工作中，原位生成的氨基烯醇中间体已被酮/醛有效捕获，用于构建N-杂环。该方法通过分子内捕获源自邻酰基/甲酰基苯胺和α-羟基二甲基缩醛/缩酮的氨基烯醇中间体，然后在酸存在下重排/芳构化，提供了具有高区域选择性的各种取代吲哚衍生物。重要特征包括使用α-羟基二甲基缩醛/缩酮作为α-羟基羰基等价物、优异的区域控制、良好的官能团耐受性、酰基吲哚的选择性合成、克级合成以及吲哚和抗肿瘤剂的高级类似物的合成。
• ANTIBIOTIC SENSITIVITY-RESTORING AND PHOTOSENSITIVE AGENTS
  申请人：New Mexico Tech Research Foundation

  公开号：US20180155286A1

  公开（公告）日：2018-06-07

  The present disclosure describes a method to treat conditions, including bacterial infections and cancer, using a photosensitive compound that, upon exposure to white light, can be activated. The photosensitive compound can also interact synergistically with antibiotics used concomitantly to kill drug-resistant bacteria. The photosensitive compounds can also be used to inhibit the proliferation of cancer cells.
• US9834514B2
  申请人：——

  公开号：US9834514B2

  公开（公告）日：2017-12-05
• [EN] ANTIBIOTIC SENSITIVITY-RESTORING AND PHOTOSENSITIVE AGENTS<br/>[FR] AGENTS PHOTOSENSIBLES ET DE RÉTABLISSEMENT DE LA SENSIBILITÉ AUX ANTIBIOTIQUES
  申请人：NEW MEXICO TECH RES FOUND

  公开号：WO2016172193A1

  公开（公告）日：2016-10-27

  The present disclosure describes a method to treat conditions, including bacterial infections and cancer, using a photosensitive compound that, upon exposure to white light, can be activated. The photosensitive compound can also interact synergistically with antibiotics used concomitantly to kill drug-resistant bacteria. The photosensitive compounds can also be used to inhibit the proliferation of cancer cells.