4-bromo-3-methyl-8-(trifluoromethyl)quinoline | 936352-89-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 4-bromo-3-methyl-8-(trifluoromethyl)quinoline
• CAS: 936352-89-5
• 化学式: C₁₁H₇BrF₃N
• 分子量: 290.082
• InChiKey: BNDFGHDMMLWMQD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  16
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  12.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-bromo-3-methyl-8-(trifluoromethyl)quinoline 在 四(三苯基膦)钯 lithium hydroxide 、 三乙酰氧基硼氢化钠 、 sodium carbonate 、 溶剂黄146 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 水 、 甲苯 、 乙腈 为溶剂， 反应 2.0h， 生成 2-{4-[({3-[3-Methyl-8-(trifluoromethyl)quinolin-4-yl]phenyl}amino)methyl]phenyl}acetic acid
  参考文献：
  名称：

  Further modification on phenyl acetic acid based quinolines as liver X receptor modulators

  摘要：

  A series of phenyl acetic acid based quinolines was prepared as LXR modulators. An SAR study in which the C-3 and C-8 positions of the quinoline core were varied led to the identification of two potent LXR agonists 23 and 27. Both compounds displayed good binding affinity for LXR beta and LXR alpha, and increased expression of ABCAl in THP-1 cells. These two compounds also had desirable pharmacokinetic profiles in mice and displayed in vivo efficacy in a 12-week Apo E knockout mouse lesion model. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2007.03.013
• 作为产物：
  描述：

  邻氨基三氟甲苯 在 diphenyl ether-biphenyl eutectic 、 sodium hydride 、 三溴氧磷 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 2.0h， 生成 4-bromo-3-methyl-8-(trifluoromethyl)quinoline
  参考文献：
  名称：

  Further modification on phenyl acetic acid based quinolines as liver X receptor modulators

  摘要：

  A series of phenyl acetic acid based quinolines was prepared as LXR modulators. An SAR study in which the C-3 and C-8 positions of the quinoline core were varied led to the identification of two potent LXR agonists 23 and 27. Both compounds displayed good binding affinity for LXR beta and LXR alpha, and increased expression of ABCAl in THP-1 cells. These two compounds also had desirable pharmacokinetic profiles in mice and displayed in vivo efficacy in a 12-week Apo E knockout mouse lesion model. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2007.03.013

文献信息

• Quinoline Acids
  申请人：Wrobel Jay E.

  公开号：US20090069373A1

  公开（公告）日：2009-03-12

  This invention relates generally to quinoline-based modulators of Liver X receptors (LXRs) and related methods.

  这项发明通常涉及喹啉基调节肝X受体（LXRs）的调节剂和相关方法。
• NOVEL QUINOLINE ESTERS USEFUL FOR TREATING SKIN DISORDERS
  申请人：Bernotas Ronald Charles

  公开号：US20120010205A1

  公开（公告）日：2012-01-12

  Disclosed are quinoline esters of Formula (I): which are useful as Liver X receptors (LXR) modulators. Pharmaceutical compositions containing quinoline esters of Formula (I) and the use of quinoline esters of Formula (I) in the safe treatment of various skin disorders are also disclosed. Methods for preparing and using quinoline esters are further described.

  公开了式(I)的喹啉酯化合物，这些化合物可用作肝X受体（LXR）调节剂。还公开了含有式(I)的喹啉酯化合物的药物组合物，以及在安全治疗各种皮肤疾病中使用式(I)的喹啉酯化合物。进一步描述了制备和使用喹啉酯的方法。
• [EN] QUINOLINE COMPOUNDS<br/>[FR] COMPOSÉS DE QUINOLÉINE
  申请人：WYETH CORP

  公开号：WO2008049047A2

  公开（公告）日：2008-04-24

  [EN] This invention relates generally to quinoline-based modulators of Liver X receptors (LXRs) and related methods.
  [FR] La présente invention concerne de manière générale des modulateurs à base de quinoléine des récepteurs X du foie (LXR) et des procédés associés.
• [EN] NOVEL QUINOLINE ESTERS USEFUL FOR TREATING SKIN DISORDERS<br/>[FR] NOUVEAUX ESTERS DE QUINOLÉINE UTILES POUR LE TRAITEMENT DE TROUBLES CUTANÉS
  申请人：WYETH LLC

  公开号：WO2012004748A1

  公开（公告）日：2012-01-12

  Disclosed are quinoline esters of Formula (I):(I) which are useful as Liver X receptors (LXR) modulators. Pharmaceutical compositions containing quinoline esters of Formula (I) and the use of quinoline esters of Formula (I) in the safe treatment of various skin disorders are also disclosed. Methods for preparing and using quinoline esters are further described.
• Further modification on phenyl acetic acid based quinolines as liver X receptor modulators
  作者：Baihua Hu、James Jetter、David Kaufman、Robert Singhaus、Ronald Bernotas、Rayomand Unwalla、Elaine Quinet、Dawn Savio、Anita Halpern、Michael Basso、James Keith、Valerie Clerin、Liang Chen、Qiang-Yuan Liu、Irene Feingold、Christine Huselton、Farooq Azam、Annika Goos-Nilsson、Anna Wilhelmsson、Ponnal Nambi、Jay Wrobel

  DOI：10.1016/j.bmc.2007.03.013

  日期：2007.5

  A series of phenyl acetic acid based quinolines was prepared as LXR modulators. An SAR study in which the C-3 and C-8 positions of the quinoline core were varied led to the identification of two potent LXR agonists 23 and 27. Both compounds displayed good binding affinity for LXR beta and LXR alpha, and increased expression of ABCAl in THP-1 cells. These two compounds also had desirable pharmacokinetic profiles in mice and displayed in vivo efficacy in a 12-week Apo E knockout mouse lesion model. (c) 2007 Elsevier Ltd. All rights reserved.