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2-(2,6-diethylphenyl)-4-methoxy-N-(5-methoxynaphthalen-1-yl)-N-methyl-5,6,7,8-tetrahydroquinolin-5-amine | 1028330-75-7

中文名称
——
中文别名
——
英文名称
2-(2,6-diethylphenyl)-4-methoxy-N-(5-methoxynaphthalen-1-yl)-N-methyl-5,6,7,8-tetrahydroquinolin-5-amine
英文别名
——
2-(2,6-diethylphenyl)-4-methoxy-N-(5-methoxynaphthalen-1-yl)-N-methyl-5,6,7,8-tetrahydroquinolin-5-amine化学式
CAS
1028330-75-7
化学式
C32H36N2O2
mdl
——
分子量
480.65
InChiKey
NACXQSITAPZCKT-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    7.7
  • 重原子数:
    36
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.34
  • 拓扑面积:
    34.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    5-氯-2-(2,6-二乙基苯基)-4-甲氧基-5,6,7,8-四氢喹啉 、 N-methylamino-5-methoxynaphthalenepotassium carbonate 作用下, 以 乙腈 为溶剂, 生成 2-(2,6-diethylphenyl)-4-methoxy-N-(5-methoxynaphthalen-1-yl)-N-methyl-5,6,7,8-tetrahydroquinolin-5-amine
    参考文献:
    名称:
    Synthesis and characterization of 5,6,7,8-tetrahydroquinoline C5a receptor antagonists
    摘要:
    A novel series of substituted 2-aryl-5-amino-5,6,7,8-tetrahydroquinoline C5a receptor antagonists is reported. Synthetic routes were developed that allow the substituents on the tetrahydroquinoline core to be efficiently varied, facilitating determination of structure-activity relationships. Members of the series display high binding affinity for the C5a receptor and are potent functional antagonists. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.03.049
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文献信息

  • Synthesis and characterization of 5,6,7,8-tetrahydroquinoline C5a receptor antagonists
    作者:J. Kent Barbay、Yong Gong、Mieke Buntinx、Jian Li、Concha Claes、Pamela J. Hornby、Guy Van Lommen、Jean Van Wauwe、Wei He
    DOI:10.1016/j.bmcl.2008.03.049
    日期:2008.4
    A novel series of substituted 2-aryl-5-amino-5,6,7,8-tetrahydroquinoline C5a receptor antagonists is reported. Synthetic routes were developed that allow the substituents on the tetrahydroquinoline core to be efficiently varied, facilitating determination of structure-activity relationships. Members of the series display high binding affinity for the C5a receptor and are potent functional antagonists. (c) 2008 Elsevier Ltd. All rights reserved.
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