8-[(3-N-ethylamino-2,6-dichlorobenzyl)oxy]-2-methyl quinoline | 617721-11-6

• 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: 8-[(3-N-ethylamino-2,6-dichlorobenzyl)oxy]-2-methyl quinoline
• 英文别名: 2,4-dichloro-N-ethyl-3-[(2-methylquinolin-8-yl)oxymethyl]aniline
• CAS: 617721-11-6
• 化学式: C₁₉H₁₈Cl₂N₂O
• 分子量: 361.271
• InChiKey: MPHODDGQYGDYCS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  24
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  34.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  [5-(4-cyano-benzoyl)-1-methyl-1H-pyrrol-2-yl]-acetyl chloride 、 8-[(3-N-ethylamino-2,6-dichlorobenzyl)oxy]-2-methyl quinoline 在 4-二甲氨基吡啶 作用下， 以 二氯甲烷 为溶剂， 生成 2-[5-(4-Cyano-benzoyl)-1-methyl-1H-pyrrol-2-yl]-N-[2,4-dichloro-3-(2-methyl-quinolin-8-yloxymethyl)-phenyl]-N-ethyl-acetamide
  参考文献：
  名称：

  Synthesis and structure–Activity relationships of aroylpyrrole alkylamide bradykinin (B2) antagonists

  摘要：

  The synthesis and structure-activity relationships of a novel series of aroylpyrrole alkylamindes as potent selective bradykinin 132 receptor antagonists are described. Several members of this series display nanomolar affinity at the B-2 receptor and show activity in an animal model of antinociception. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00104-5
• 作为产物：
  描述：

  8-(2,6-dichloro-3-aminobenzyloxy)-2-methylquinoline 在 sodium tetrahydroborate 、 sodium hydride 作用下， 以 甲醇 、 氯仿 、 N,N-二甲基甲酰胺 为溶剂， 生成 8-[(3-N-ethylamino-2,6-dichlorobenzyl)oxy]-2-methyl quinoline
  参考文献：
  名称：

  Synthesis and structure–Activity relationships of aroylpyrrole alkylamide bradykinin (B2) antagonists

  摘要：

  The synthesis and structure-activity relationships of a novel series of aroylpyrrole alkylamindes as potent selective bradykinin 132 receptor antagonists are described. Several members of this series display nanomolar affinity at the B-2 receptor and show activity in an animal model of antinociception. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00104-5

文献信息

• Novel heteroaryl alkylamide derivatives useful as bradykinin receptor modulators
  申请人：——

  公开号：US20040192720A1

  公开（公告）日：2004-09-30

  This invention is directed towards novel alkylamide derivatives as bradykinin receptor antagonists useful for the treatment of bradykinin modulated disorders such as pain, inflammation, asthma and allergy. Furthermore, the present invention is directed to novel alkylamide derivatives as bradykinin receptor agonists useful for the treatment of bradykinin modulated disorders such as hypertension and the like.

  这项发明涉及新颖的烷基酰胺衍生物，作为布雷金肽受体拮抗剂，用于治疗布雷金肽调节的疾病，如疼痛、炎症、哮喘和过敏。此外，该发明涉及新颖的烷基酰胺衍生物，作为布雷金肽受体激动剂，用于治疗布雷金肽调节的疾病，如高血压等。
• US6958349B2
  申请人：——

  公开号：US6958349B2

  公开（公告）日：2005-10-25
• US7358261B2
  申请人：——

  公开号：US7358261B2

  公开（公告）日：2008-04-15
• Synthesis and structure–Activity relationships of aroylpyrrole alkylamide bradykinin (B2) antagonists
  作者：Mark A. Youngman、John R. Carson、Jung S. Lee、Scott L. Dax、Sui-Po Zhang、Ray W. Colburn、Dennis J. Stone、Ellen E. Codd、Michele C. Jetter

  DOI：10.1016/s0960-894x(03)00104-5

  日期：2003.4

  The synthesis and structure-activity relationships of a novel series of aroylpyrrole alkylamindes as potent selective bradykinin 132 receptor antagonists are described. Several members of this series display nanomolar affinity at the B-2 receptor and show activity in an animal model of antinociception. (C) 2003 Elsevier Science Ltd. All rights reserved.