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1-[2-Amino-3-(2,6-dimethoxy-benzoyl)-4,7-dihydro-5H-thieno[2,3-c]pyridin-6-yl]-ethanone | 847951-04-6

中文名称
——
中文别名
——
英文名称
1-[2-Amino-3-(2,6-dimethoxy-benzoyl)-4,7-dihydro-5H-thieno[2,3-c]pyridin-6-yl]-ethanone
英文别名
——
1-[2-Amino-3-(2,6-dimethoxy-benzoyl)-4,7-dihydro-5H-thieno[2,3-c]pyridin-6-yl]-ethanone化学式
CAS
847951-04-6
化学式
C18H20N2O4S
mdl
——
分子量
360.434
InChiKey
MERLPAHOICOHFK-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

物化性质

  • 沸点:
    658.6±55.0 °C(Predicted)
  • 密度:
    1.303±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.48
  • 重原子数:
    25.0
  • 可旋转键数:
    4.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    81.86
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    1-[2-Amino-3-(2,6-dimethoxy-benzoyl)-4,7-dihydro-5H-thieno[2,3-c]pyridin-6-yl]-ethanone 、 alkaline earth salt of/the/ methylsulfuric acid 在 吡啶 作用下, 生成 N-[6-acetyl-3-(2,6-dimethoxybenzoyl)-5,7-dihydro-4H-thieno[2,3-c]pyridin-2-yl]acetamide
    参考文献:
    名称:
    Synthesis and bioactivities of novel 4,5,6,7-Tetrahydrothieno[2,3-c]pyridines as inhibitors of tumor necrosis factor-α (TNF-α) production
    摘要:
    Novel 4,5,6,7-tetraliydrothieno[2,3-c]pyridine derivatives were synthesized and evaluated for their abilities to inhibit lipopolysaccharide (LPS)-stimulated production of TNF-alpha in rat whole blood. Several of these compounds exhibited potent inhibitory activity. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00228-7
  • 作为产物:
    参考文献:
    名称:
    Synthesis and bioactivities of novel 4,5,6,7-Tetrahydrothieno[2,3-c]pyridines as inhibitors of tumor necrosis factor-α (TNF-α) production
    摘要:
    Novel 4,5,6,7-tetraliydrothieno[2,3-c]pyridine derivatives were synthesized and evaluated for their abilities to inhibit lipopolysaccharide (LPS)-stimulated production of TNF-alpha in rat whole blood. Several of these compounds exhibited potent inhibitory activity. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00228-7
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