8-tert-butyl-1-methyl-2,3-dihydroquinolin-4(1H)-one O-methyl oxime | 1034770-75-6

• 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-tert-butyl-1-methyl-2,3-dihydroquinolin-4(1H)-one O-methyl oxime
• 英文别名: 8-tert-Butyl-1-methyl-2,3-dihydroquinolin-4(1H)-one O-methyl oxime；8-tert-butyl-N-methoxy-1-methyl-2,3-dihydroquinolin-4-imine
• CAS: 1034770-75-6
• 化学式: C₁₅H₂₂N₂O
• 分子量: 246.352
• InChiKey: OHYVAXITPKCDKX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  24.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  8-tert-butyl-1-methyl-2,3-dihydroquinolin-4(1H)-one O-methyl oxime 在 氨 、 氢气 、 N,N-二异丙基乙胺 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 20.0 ℃ 、413.7 kPa 条件下， 反应 4.5h， 生成
  参考文献：
  名称：

  Chroman and tetrahydroquinoline ureas as potent TRPV1 antagonists

  摘要：

  Novel chroman and tetrahydroquinoline ureas were synthesized and evaluated for their activity as TRPV1 antagonists. It was found that aryl substituents on the 7- or 8-position of both bicyclic scaffolds imparted the best in vitro potency at TRPV1. The most potent chroman ureas were assessed in chronic and acute pain models, and compounds with the ability to cross the blood-brain barrier were shown to be highly efficacious. The tetrahydroquinoline ureas were found to be potent CYP3A4 inhibitors, but replacement of bulky substituents at the nitrogen atom of the tetrahydroisoquinoline moiety with small groups such as methyl can minimize the inhibition. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.01.056
• 作为产物：
  描述：

  甲氧基胺盐酸盐 、 8-tert-Butyl-1-methyl-2,3-dihydroquinolin-4(1H)-one 在 乙酸乙酯 、 水 、 Brine 、 Sodium sulfate-III 、 silica gel 、 正己烷 作用下， 以 吡啶 为溶剂， 反应 16.0h， 生成 8-tert-butyl-1-methyl-2,3-dihydroquinolin-4(1H)-one O-methyl oxime
  参考文献：
  名称：

  ANTAGONISTS OF THE TRPV1 RECEPTOR AND USES THEREOF

  摘要：

  本申请涉及的是化合物，其为TRPV1拮抗剂，具有式（I），其中变量Ar1、L1、R1、R2、R3、R4、R5、Y1、Y2和Y3如说明书所定义，对于治疗由vanilloid受体活性引起或加剧的疾病有用。

  公开号：

  US20130165479A1

文献信息

• Antagonists of the TRPV1 receptor and uses thereof
  申请人：Abbott Laboratories

  公开号：US08030504B2

  公开（公告）日：2011-10-04

  The present application is directed to compounds that are TRPV1 antagonists and have formula (I) wherein variables Ar1, L1, R1, R2, R3, R4, R5, Y1, Y2, and Y3, are as defined in the description, which are useful for treating disorders caused by or exacerbated by vanilloid receptor activity.

  本申请涉及化合物，其为TRPV1拮抗剂，具有公式(I)，其中变量Ar1、L1、R1、R2、R3、R4、R5、Y1、Y2和Y3如描述中所定义，其可用于治疗由vanilloid受体活性引起或加重的疾病。
• ANTAGONISTS OF THE TRPV1 RECEPTOR AND USES THEREOF
  申请人：Bayburt Erol K.

  公开号：US20080153871A1

  公开（公告）日：2008-06-26

  The present application is directed to compounds that are TRPV1 antagonists and have formula (I) wherein variables Ar 1 , L 1 , R 1 , R 2 , R 3 , R 4 , R 5 , Y 1 , Y 2 , and Y 3 , are as defined in the description, which are useful for treating disorders caused by or exacerbated by vanilloid receptor activity.

  本申请涉及的化合物是TRPV1拮抗剂，其化学式为（I），其中变量Ar1，L1，R1，R2，R3，R4，R5，Y1，Y2和Y3如描述中所定义，对于治疗由辣椒素受体活性引起或加剧的疾病是有用的。
• Chroman and tetrahydroquinoline ureas as potent TRPV1 antagonists
  作者：Robert G. Schmidt、Erol K. Bayburt、Steven P. Latshaw、John R. Koenig、Jerome F. Daanen、Heath A. McDonald、Bruce R. Bianchi、Chengmin Zhong、Shailen Joshi、Prisca Honore、Kennan C. Marsh、Chih-Hung Lee、Connie R. Faltynek、Arthur Gomtsyan

  DOI：10.1016/j.bmcl.2011.01.056

  日期：2011.3

  Novel chroman and tetrahydroquinoline ureas were synthesized and evaluated for their activity as TRPV1 antagonists. It was found that aryl substituents on the 7- or 8-position of both bicyclic scaffolds imparted the best in vitro potency at TRPV1. The most potent chroman ureas were assessed in chronic and acute pain models, and compounds with the ability to cross the blood-brain barrier were shown to be highly efficacious. The tetrahydroquinoline ureas were found to be potent CYP3A4 inhibitors, but replacement of bulky substituents at the nitrogen atom of the tetrahydroisoquinoline moiety with small groups such as methyl can minimize the inhibition. (C) 2011 Elsevier Ltd. All rights reserved.