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N-[2-(1-benzylpiperidin-4-yl)ethyl]acetamide | 203663-04-1

中文名称
——
中文别名
——
英文名称
N-[2-(1-benzylpiperidin-4-yl)ethyl]acetamide
英文别名
——
N-[2-(1-benzylpiperidin-4-yl)ethyl]acetamide化学式
CAS
203663-04-1
化学式
C16H24N2O
mdl
——
分子量
260.379
InChiKey
IVZYWMPKDTZXNJ-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):
    2.2
  • 重原子数:
    19
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    N-[2-(1-benzylpiperidin-4-yl)ethyl]acetamide 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 以85%的产率得到2-(1-benzylpiperidin-4-yl)-N-ethylethanamine
    参考文献:
    名称:
    Vidaluc; Calmel; Bigg, Journal of Medicinal Chemistry, 1994, vol. 37, # 5, p. 689 - 695
    摘要:
    DOI:
  • 作为产物:
    描述:
    4-(2-氨基乙基)-1-苄基哌啶乙酰氯三乙胺 作用下, 以 二氯甲烷 为溶剂, 以53%的产率得到N-[2-(1-benzylpiperidin-4-yl)ethyl]acetamide
    参考文献:
    名称:
    Vidaluc; Calmel; Bigg, Journal of Medicinal Chemistry, 1994, vol. 37, # 5, p. 689 - 695
    摘要:
    DOI:
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文献信息

  • Thienopyrrole compound and use thereof as HCV polymerase inhibitor
    申请人:Mizojiri Ryo
    公开号:US20060167246A1
    公开(公告)日:2006-07-27
    The present invention relates to a thienopyrrole compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable a salt thereof, and a hepatitis C virus (HCV) polymerase inhibitor and a therapeutic agent for hepatitis C containing this compound as an active ingredient. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及一种由下式[I]所表示的噻吡咯烷化合物,其中每个符号如规范中定义,或其药学上可接受的盐,以及一种丙型肝炎病毒(HCV)聚合酶抑制剂和含有该化合物作为活性成分的治疗剂。本发明的化合物基于HCV聚合酶抑制活性显示抗HCV活性,并且可用作丙型肝炎的预防或治疗剂。
  • 5-5-Membered fused heterocyclic compound and use thereof as HCV polymerase inhibitor
    申请人:Mizojiri Ryo
    公开号:US20090036444A1
    公开(公告)日:2009-02-05
    The present invention relates to a fused ring compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable a salt thereof, and a hepatitis C virus (HCV) polymerase inhibitor and a therapeutic agent for hepatitis C containing this compound. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及一种由以下式[I]表示的融合环化合物,其中每个符号如规范中所定义,或其药学上可接受的盐,以及一种丙型肝炎病毒(HCV)聚合酶抑制剂和治疗丙型肝炎的药物,本发明的化合物基于HCV聚合酶抑制活性具有抗HCV活性,是一种预防或治疗丙型肝炎的药剂。
  • Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor
    申请人:Oka Takahiro
    公开号:US20070049593A1
    公开(公告)日:2007-03-01
    The present invention relates to a tetracyclic fused heterocyclic compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable a salt thereof, and a hepatitis C virus (HCV) polymerase inhibitor and a therapeutic agent for hepatitis C containing this compound. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及一种四环融合杂环化合物,其化学式为[I],其中每个符号的定义如规范中所述,或其药学上可接受的盐,以及一种丙型肝炎病毒(HCV)聚合酶抑制剂和治疗丙型肝炎的药物,本发明的化合物表现出基于HCV聚合酶抑制活性的抗HCV活性,因此可用作预防或治疗丙型肝炎的药物。
  • TETRACYCLIC FUSED HETEROCYCLIC COMPOUND AND USE THEREOF AS HCV POLYMERASE INHIBITOR
    申请人:Oka Takahiro
    公开号:US20120070409A1
    公开(公告)日:2012-03-22
    The present invention relates to a tetracyclic fused heterocyclic compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable a salt thereof, and a hepatitis C virus (HCV) polymerase inhibitor and a therapeutic agent for hepatitis C containing this compound. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及一种四环融合杂环化合物,其表示为以下公式[I],其中每个符号如规范中所定义,或其药学上可接受的盐,以及一种丙型肝炎病毒(HCV)聚合酶抑制剂和治疗丙型肝炎的药物,本发明的化合物基于HCV聚合酶抑制活性显示出抗HCV活性,可用作预防或治疗丙型肝炎的药物。
  • 5-5-MEMBERED FUSED HETEROCYCLIC COMPOUND AND USE THEREOF AS HCV POLYMERASE INHIBITOR
    申请人:Mizojiri Ryo
    公开号:US20120020920A1
    公开(公告)日:2012-01-26
    The present invention relates to a fused ring compound represented by the following formula [I] wherein each symbol is as defined in the specification, or a pharmaceutically acceptable a salt thereof, and a hepatitis C virus (HCV) polymerase inhibitor and a therapeutic agent for hepatitis C containing this compound. The compound of the present invention shows an anti-HCV activity based on the HCV polymerase inhibitory activity, and useful as an agent for the prophylaxis or treatment of hepatitis C.
    本发明涉及一种由以下式[I]所表示的融合环化合物,其中每个符号如规范中所定义,或其药学上可接受的盐,以及一种丙型肝炎病毒(HCV)聚合酶抑制剂和治疗丙型肝炎的药物,本发明化合物基于HCV聚合酶抑制活性具有抗HCV活性,可用作预防或治疗丙型肝炎的药剂。
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