2-(5-bromoindolin-2-yl)-5-chloro-3-fluorophenol | 1620450-60-3

• 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: 2-(5-bromoindolin-2-yl)-5-chloro-3-fluorophenol
• 英文别名: 2-(5-Bromo-2,3-dihydro-1H-indol-2-yl)-5-chloro-3-fluorophenol；2-(5-bromo-2,3-dihydro-1H-indol-2-yl)-5-chloro-3-fluorophenol
• CAS: 1620450-60-3
• 化学式: C₁₄H₁₀BrClFNO
• 分子量: 342.595
• InChiKey: QVWUHQWCIQNZAE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  32.3
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(5-bromoindolin-2-yl)-5-chloro-3-fluorophenol 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 三乙胺 、 三氟乙酸 、 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 N,N-二甲基甲酰胺 、 甲苯 、 乙腈 为溶剂， 20.0~110.0 ℃ 、344.75 kPa 条件下， 反应 65.5h， 生成 methyl 3-chloro-6-(2-cyclopropyl-1,3-thiazol-5-yl)-1-fluoro-6H-indolo[1,2-c][1,3]benzoxazine-10-carboxylate
  参考文献：
  名称：

  [EN] HETEROCYCLE-SUBSTITUTED TETRACYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR TREATMENT OF VIRAL DISEASES
  [FR] COMPOSÉS TÉTRACYCLIQUES SUBSTITUÉS PAR UN HÉTÉROCYCLE ET PROCÉDÉS POUR LES UTILISER POUR LE TRAITEMENT DE MALADIES VIRALES

  摘要：

  公开号：

  WO2014110705A9
• 作为产物：
  描述：

  2-(5-bromo-1H-indol-2-yl)-5-chloro-3-fluorophenol 在 三氟乙酸 、 锌 作用下， 反应 24.0h， 以53.3%的产率得到2-(5-bromoindolin-2-yl)-5-chloro-3-fluorophenol
  参考文献：
  名称：

  [EN] THIOPHENE-SUBSTITUTED TETRACYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR TREATMENT OF VIRAL DISEASES
  [FR] COMPOSÉS TÉTRACYCLIQUES À SUBSTITUTION THIOPHÈNE ET LEURS MÉHODES D'UTILISATION POUR LE TRAITEMENT DE MALADIES VIRALES

  摘要：

  式(I)的噻吩取代四环化合物及其药用可接受的盐，其中A、A'、R2、R3、R4和R5如本文所定义。还提供了包含至少一种噻吩取代四环化合物的组合物，以及使用这些噻吩取代四环化合物治疗或预防患者HCV感染的方法。

  公开号：

  WO2014110706A1

文献信息

• [EN] THIOPHENE- SUB STITUED TETRACYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES<br/>[FR] COMPOSÉS TÉTRACYCLIQUES À SUBSTITUTION THIOPHÈNE ET LEURS PROCÉDÉS D'UTILISATION POUR LE TRAITEMENT DES MALADIES VIRALES
  申请人：MERCK SHARP & DOHME

  公开号：WO2014110688A1

  公开（公告）日：2014-07-24

  Disclosed are novel Thiophene-Subsituted Tetracyclic Compounds of Formula (I). And pharmaceutically acceptable salts thereof, wherein A, A', R2, R3, R4 and R5 are as defined herein. The compositions comprising at least one Thiophene-Subsituted Tetracyclic Compounds, and methods of using the Thiophene-Subsituted Tetracyclic Compounds for treating or preventing HCV infection in a patient are also disclosed.

  本发明涉及一种新颖的式(I)的噻吩取代四环化合物，以及其药学上可接受的盐，其中A、A'、R2、R3、R4和R5如本文所定义。还公开了包含至少一种噻吩取代四环化合物的组合物，以及使用这些噻吩取代四环化合物治疗或预防患者HCV感染的方法。
• [EN] THIOPHENE-SUBSTITUTED TETRACYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR TREATMENT OF VIRAL DISEASES<br/>[FR] COMPOSÉS TÉTRACYCLIQUES À SUBSTITUTION THIOPHÈNE ET LEURS MÉHODES D'UTILISATION POUR LE TRAITEMENT DE MALADIES VIRALES
  申请人：MERCK SHARP & DOHME

  公开号：WO2014110706A1

  公开（公告）日：2014-07-24

  Thiophene-substituted tetracyclic compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein A, A', R2, R3, R4 and R5 are as defined herein. The compositions comprising at least one thiophene-substituted tetracyclic compound, and methods of using the thiophene-substituted tetracyclic compounds for treating or preventing HCV infection in a patient are also provided.

  式(I)的噻吩取代四环化合物及其药用可接受的盐，其中A、A'、R2、R3、R4和R5如本文所定义。还提供了包含至少一种噻吩取代四环化合物的组合物，以及使用这些噻吩取代四环化合物治疗或预防患者HCV感染的方法。
• Discovery of MK-6169, a Potent Pan-Genotype Hepatitis C Virus NS5A Inhibitor with Optimized Activity against Common Resistance-Associated Substitutions
  作者：Wensheng Yu、Ling Tong、Oleg Selyutin、Lei Chen、Bin Hu、Bin Zhong、Jinglai Hao、Tao Ji、Shuai Zan、Jingjun Yin、Rebecca T. Ruck、Stephanie Curry、Patricia McMonagle、Sony Agrawal、Laura Rokosz、Donna Carr、Paul Ingravallo、Karin Bystol、Frederick Lahser、Rong Liu、Shiying Chen、Kung-I Feng、Mark Cartwright、Ernest Asante-Appiah、Joseph A. Kozlowski

  DOI：10.1021/acs.jmedchem.7b01927

  日期：2018.5.10

  We describe the discovery of MK-6169, a potent and pan-genotype hepatitis C virus NS5A inhibitor with optimized activity against common resistance-associated substitutions. SAR studies around the combination of changes to both the valine and aminal carbon region of elbasvir led to the discovery of a series of compounds with substantially improved potency against common resistance-associated substitutions in the major genotypes, as well as good pharmacokinetics in both rat and dog. Through further optimization of key leads from this effort, MK-6169 (21) was discovered as a preclinical candidate for further development.
• HETEROCYCLE-SUBSTITUTED TETRACYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES
  申请人：MERCK SHARP & DOHME CORP.

  公开号：US20150335648A1

  公开（公告）日：2015-11-26

  The present invention relates to novel Heterocycle-Substituted Tetracyclic Compounds of Formula (I): (I) and pharmaceutically acceptable salts thereof, wherein A, A′, R 2 R 3 , R 4 and R are as defined herein. The present invention also relates to compositions comprising at least one Heterocycle-Substituted Tetracyclic Compound, and methods of using the Heterocycle-Substituted Tetracyclic Compounds for treating or preventing HCV infection in a patient.
• THIOPHENE-SUBSTITUTED TETRACYCLIC COMPOUNDS AND METHODS OFUSE THEREOF FOR THE TREATMENT OF VIRAL DISEASES
  申请人：MERCK SHARP & DOHME CORP.

  公开号：US20160257697A1

  公开（公告）日：2016-09-08

  Thiophene-substituted tetracyclic compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein A, A′, R 2 , R 3 , R 4 and R 5 are as defined herein. The compositions comprising at least one thiophene-substituted tetracyclic compound, and methods of using the thiophene-substituted tetracyclic compounds for treating or preventing HCV infection in a patient are also provided.