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(3R)-3-(methoxymethyl)piperidine

中文名称
——
中文别名
——
英文名称
(3R)-3-(methoxymethyl)piperidine
英文别名
——
(3R)-3-(methoxymethyl)piperidine化学式
CAS
——
化学式
C7H15NO
mdl
——
分子量
129.202
InChiKey
ZVNNEPYIBDITIW-SSDOTTSWSA-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):
    0.4
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    21.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    (3R)-3-(methoxymethyl)piperidine氯乙酰胺 在 sodium hydroxide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 以21%的产率得到3-amino-4-[(3R)-3-(methoxymethyl)piperidin-1-yl]thieno[2,3-b]pyridine-2-carboxamide
    参考文献:
    名称:
    Discovery of 3-amino-4-{(3S)-3-[(2-ethoxyethoxy)methyl]piperidin-1-yl}thieno[2,3-b]pyridine-2-carboxamide (DS96432529): A potent and orally active bone anabolic agent
    摘要:
    DOI:
    10.1016/j.bmcl.2021.128440
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文献信息

  • 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。
  • Fused heterotetracyclic compounds and use thereof as hcv polymerase inhibitor
    申请人:Japan Tobacco, Inc.
    公开号:EP2206715A1
    公开(公告)日:2010-07-14
    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.
    本发明涉及由下式[I]表示的四环融合杂环化合物 其中各符号如说明书中所定义,或其药学上可接受的盐,以及含有该化合物的丙型肝炎病毒(HCV)聚合酶抑制剂和丙型肝炎治疗剂。本发明的化合物具有基于 HCV 聚合酶抑制活性的抗 HCV 活性,可用作丙型肝炎的预防或治疗剂。
  • FUSED HETEROTETRACYCLIC COMPOUNDS AND USE TEHREOF AS HCV POLYMERASE INHIBITOR
    申请人:Japan Tobacco, Inc.
    公开号:EP1719773B1
    公开(公告)日:2009-04-15
  • US7667036B2
    申请人:——
    公开号:US7667036B2
    公开(公告)日:2010-02-23
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