6-(Benzyloxy)-4-chloro-7-methoxy-3-quinolinecarboxylic acid | 476193-58-5

• 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: 6-(Benzyloxy)-4-chloro-7-methoxy-3-quinolinecarboxylic acid
• 英文别名: 4-chloro-7-methoxy-6-phenylmethoxyquinoline-3-carboxylic acid
• CAS: 476193-58-5
• 化学式: C₁₈H₁₄ClNO₄
• 分子量: 343.766
• InChiKey: PKPULJQIMPSBKD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  24
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  68.6
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  6-(Benzyloxy)-4-chloro-7-methoxy-3-quinolinecarboxylic acid 在 氯化亚砜 作用下， 以 甲苯 为溶剂， 反应 2.0h， 生成 4-Chloro-7-methoxy-6-phenylmethoxyquinoline-3-carbonyl chloride
  参考文献：
  名称：

  Identification of 3-amido-4-anilinoquinolines as potent and selective inhibitors of CSF-1R kinase

  摘要：

  3-Amido-4-anilinoquinolines are potent and highly selective inhibitors of CSF-1R. Their synthesis and SAR is reported, along with initial efforts to optimize the physical properties and PK through modi. cations at the quinoline 6- and 7-positions. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.12.046
• 作为产物：
  描述：

  ethyl 6-(benzyloxy)-4-chloro-7-methoxyquinoline-3-carboxylate 在 sodium hydroxide 、 水 作用下， 以 甲醇 为溶剂， 生成 6-(Benzyloxy)-4-chloro-7-methoxy-3-quinolinecarboxylic acid
  参考文献：
  名称：

  Identification of 3-amido-4-anilinoquinolines as potent and selective inhibitors of CSF-1R kinase

  摘要：

  3-Amido-4-anilinoquinolines are potent and highly selective inhibitors of CSF-1R. Their synthesis and SAR is reported, along with initial efforts to optimize the physical properties and PK through modi. cations at the quinoline 6- and 7-positions. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.12.046

文献信息

• Novel 4-anilinoquinoline-3-carboxamides
  申请人：——

  公开号：US20040248923A1

  公开（公告）日：2004-12-09

  The present invention relates to novel compounds of formula (IA), which are JAK3 Kinase inhibitors, methods for their preparation and pharmaceutical compositions comprising them.

  本发明涉及公式（IA）的新型化合物，它们是JAK3激酶抑制剂，以及它们的制备方法和包含它们的药物组合物。
• 4-anilinoquinoline-3-carboxamides
  申请人：AstraZeneca AB

  公开号：US07037925B2

  公开（公告）日：2006-05-02

  The present invention relates to novel compounds of formula (IA), which are JAK3 Kinase inhibitors, methods for their preparation and pharmaceutical compositions comprising them.

  本发明涉及一种新型化合物（IA式），它们是JAK3激酶抑制剂，以及它们的制备方法和包含它们的药物组合物。
• NOVEL 4-ANILINOQUINOLINE-3-CARBOXAMIDES
  申请人：AstraZeneca AB

  公开号：EP1387830A1

  公开（公告）日：2004-02-11
• US7037925B2
  申请人：——

  公开号：US7037925B2

  公开（公告）日：2006-05-02
• [EN] NOVEL 4-ANILINOQUINOLINE-3-CARBOXAMIDES<br/>[FR] NOUVEAUX 4-ANILINOQUINOLINE-3-CARBOXAMIDES
  申请人：ASTRAZENECA AB

  公开号：WO2002092571A1

  公开（公告）日：2002-11-21

  The present invention relates to novel compounds of formula (IA), which are JAK3 Kinase inhibitors, methods for their preparation and pharmaceutical compositions comprising them.