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N-(1-Methyl-1,2,3,4-tetrahydro-quinolin-8-yl)-acetamide | 908595-93-7

中文名称
——
中文别名
——
英文名称
N-(1-Methyl-1,2,3,4-tetrahydro-quinolin-8-yl)-acetamide
英文别名
N-(1-methyl-3,4-dihydro-2H-quinolin-8-yl)acetamide
N-(1-Methyl-1,2,3,4-tetrahydro-quinolin-8-yl)-acetamide化学式
CAS
908595-93-7
化学式
C12H16N2O
mdl
MFCD24392124
分子量
204.272
InChiKey
JOOWWUPNMHASEI-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):
    1.6
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.416
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    N-(1-Methyl-1,2,3,4-tetrahydro-quinolin-8-yl)-acetamide盐酸4-二甲氨基吡啶盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 生成 N-(1-methyl-3,4-dihydro-2H-quinolin-8-yl)-4-phenylbenzamide
    参考文献:
    名称:
    N-Tetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl biaryl carboxamides as antagonists of TRPV1
    摘要:
    Starting from the high throughput screening hit (3), novel N-tetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl carboxamides have been identified as potent antagonists of the ion channel TRPV1. The N-quinolinylnicotinamide (46) showed excellent potency at human, guinea pig and rat TRPV1, a favourable in vitro DMPK profile and activity in an in vivo model of inflammatory pain. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.06.026
  • 作为产物:
    描述:
    参考文献:
    名称:
    N-Tetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl biaryl carboxamides as antagonists of TRPV1
    摘要:
    Starting from the high throughput screening hit (3), novel N-tetrahydroquinolinyl, N-quinolinyl and N-isoquinolinyl carboxamides have been identified as potent antagonists of the ion channel TRPV1. The N-quinolinylnicotinamide (46) showed excellent potency at human, guinea pig and rat TRPV1, a favourable in vitro DMPK profile and activity in an in vivo model of inflammatory pain. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.06.026
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