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5,6-tetramethylene-4-carboethixy-2-pyridone | 126814-00-4

中文名称
——
中文别名
——
英文名称
5,6-tetramethylene-4-carboethixy-2-pyridone
英文别名
ethyl 2-oxo-1,2,5,6,7,8-hexahydroquinoline-4-carboxylate;Ethyl 1,2,5,6,7,8-hexahydro-2-oxoquinoline-4-carboxylate;ethyl 2-oxo-5,6,7,8-tetrahydro-1H-quinoline-4-carboxylate
5,6-tetramethylene-4-carboethixy-2-pyridone化学式
CAS
126814-00-4
化学式
C12H15NO3
mdl
——
分子量
221.256
InChiKey
SMRKOKAMQPFGLS-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):
    0.9
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    55.4
  • 氢给体数:
    1
  • 氢受体数:
    3

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:
    5,6-tetramethylene-4-carboethixy-2-pyridone一水合肼 作用下, 以 乙醇 为溶剂, 反应 10.0h, 以75%的产率得到2-oxo-1,2,5,6,7,8-hexahydroquinoline-4-carbohydrazide
    参考文献:
    名称:
    Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents
    摘要:
    A series of fused and functionalized pyridine derivatives were designed, synthesized and tested for their potential antitubercular properties. All these novel compounds were prepared by using multistep methods involving the construction of pyridine ring as a key synthetic step. Some of these compounds were found to be interesting when tested for their antitubercular properties in vitro and one of them appeared as an attractive and potential antitubercular agent. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.05.096
  • 作为产物:
    描述:
    环己酮乙醇硫酸 、 sodium hydride 、 乙酰氯 作用下, 反应 42.0h, 生成 5,6-tetramethylene-4-carboethixy-2-pyridone
    参考文献:
    名称:
    Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents
    摘要:
    A series of fused and functionalized pyridine derivatives were designed, synthesized and tested for their potential antitubercular properties. All these novel compounds were prepared by using multistep methods involving the construction of pyridine ring as a key synthetic step. Some of these compounds were found to be interesting when tested for their antitubercular properties in vitro and one of them appeared as an attractive and potential antitubercular agent. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.05.096
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文献信息

  • Antiinflammation agents
    申请人:Browner F. Michelle
    公开号:US20070135464A1
    公开(公告)日:2007-06-14
    Compounds, compositions and methods that are useful in the treatment of inflammatory, immunoregulatory, metabolic and cell proliferative conditions or diseases are provided herein. In particular, the invention provides compounds which modulate the expression and/or function of proteins involved in inflammation, metabolism and cell proliferation. The subject compounds contain fused carbocyclic or heterocyclic rings.
    本文提供了在治疗炎症、免疫调节、代谢和细胞增殖状况或疾病中有用的化合物、组合物和方法。特别地,本发明提供了调节参与炎症、代谢和细胞增殖的蛋白质表达和/或功能的化合物。所述化合物包含融合的碳环或杂环环。
  • Lowe, John A.; Ewing, Frank E.; Drozda, Susan E., Synthetic Communications, 1989, vol. 19, # 17, p. 3027 - 3036
    作者:Lowe, John A.、Ewing, Frank E.、Drozda, Susan E.
    DOI:——
    日期:——
  • US7186841B2
    申请人:——
    公开号:US7186841B2
    公开(公告)日:2007-03-06
  • Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents
    作者:Balakrishna Dulla、Baojie Wan、Scott G. Franzblau、Ravikumar Kapavarapu、Oliver Reiser、Javed Iqbal、Manojit Pal
    DOI:10.1016/j.bmcl.2012.05.096
    日期:2012.7
    A series of fused and functionalized pyridine derivatives were designed, synthesized and tested for their potential antitubercular properties. All these novel compounds were prepared by using multistep methods involving the construction of pyridine ring as a key synthetic step. Some of these compounds were found to be interesting when tested for their antitubercular properties in vitro and one of them appeared as an attractive and potential antitubercular agent. (C) 2012 Elsevier Ltd. All rights reserved.
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