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Ethyl 4-(4,7-dichloro-1,8-naphthyridin-2-yl)piperazine-1-carboxylate | 210643-21-3

中文名称
——
中文别名
——
英文名称
Ethyl 4-(4,7-dichloro-1,8-naphthyridin-2-yl)piperazine-1-carboxylate
英文别名
——
Ethyl 4-(4,7-dichloro-1,8-naphthyridin-2-yl)piperazine-1-carboxylate化学式
CAS
210643-21-3
化学式
C15H16Cl2N4O2
mdl
——
分子量
355.224
InChiKey
SDOWCXAXYMMRDE-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):
    3.5
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    58.6
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    Ethyl 4-(4,7-dichloro-1,8-naphthyridin-2-yl)piperazine-1-carboxylatesodium hydroxide 作用下, 以 甲醇 为溶剂, 反应 12.0h, 生成 4-Chloro-7-methoxy-2-piperazin-1-yl-1,8-naphthyridine
    参考文献:
    名称:
    Synthesis of 1,8-naphthyridine derivatives: Potential antihypertensive agents — Part VII
    摘要:
    A series of 2-(carbethoxypiperazinyl)- and 2-piperazinyl-1,8-naphthyridine derivatives, variously substituted, have been synthesized and pharmacologically investigated for their antihypertensive activity. Some of them exhibited a significant and prolonged decrease of the mean arterial pressure (MAP) on spontaneously hypertensive rats. For this series of compounds, on the basis of the pharmacological results obtained, no structure-activity relationship can be deduced at this time. Moreover, the most active and representative compounds 11b, 12a and 16b were investigated by means of in vitro pharmacological functional studies and in vivo, as diuretic agents, to determine a possible mechanism of the antihypertensive activity, which is unknown for the moment. (C) Elsevier, Paris.
    DOI:
    10.1016/s0223-5234(98)80014-7
  • 作为产物:
    描述:
    2,6-二氨基吡啶ammonium hydroxide硫酸三乙胺 、 sodium nitrite 、 三氯氧磷 作用下, 以 二苯醚 为溶剂, 反应 35.0h, 生成 Ethyl 4-(4,7-dichloro-1,8-naphthyridin-2-yl)piperazine-1-carboxylate
    参考文献:
    名称:
    Synthesis of 1,8-naphthyridine derivatives: Potential antihypertensive agents — Part VII
    摘要:
    A series of 2-(carbethoxypiperazinyl)- and 2-piperazinyl-1,8-naphthyridine derivatives, variously substituted, have been synthesized and pharmacologically investigated for their antihypertensive activity. Some of them exhibited a significant and prolonged decrease of the mean arterial pressure (MAP) on spontaneously hypertensive rats. For this series of compounds, on the basis of the pharmacological results obtained, no structure-activity relationship can be deduced at this time. Moreover, the most active and representative compounds 11b, 12a and 16b were investigated by means of in vitro pharmacological functional studies and in vivo, as diuretic agents, to determine a possible mechanism of the antihypertensive activity, which is unknown for the moment. (C) Elsevier, Paris.
    DOI:
    10.1016/s0223-5234(98)80014-7
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文献信息

  • Synthesis of 1,8-naphthyridine derivatives: Potential antihypertensive agents — Part VII
    作者:Pier Luigi Ferrarini、Claudio Mori、Muwaffag Badawneh、Vincenzo Calderone、Lorella Calzolari、Tiziana Loffredo、Enrica Martinotti、Giuseppe Saccomanni
    DOI:10.1016/s0223-5234(98)80014-7
    日期:1998.6
    A series of 2-(carbethoxypiperazinyl)- and 2-piperazinyl-1,8-naphthyridine derivatives, variously substituted, have been synthesized and pharmacologically investigated for their antihypertensive activity. Some of them exhibited a significant and prolonged decrease of the mean arterial pressure (MAP) on spontaneously hypertensive rats. For this series of compounds, on the basis of the pharmacological results obtained, no structure-activity relationship can be deduced at this time. Moreover, the most active and representative compounds 11b, 12a and 16b were investigated by means of in vitro pharmacological functional studies and in vivo, as diuretic agents, to determine a possible mechanism of the antihypertensive activity, which is unknown for the moment. (C) Elsevier, Paris.
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