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tert-butyl [5-(5-(ethoxymethoxy)-2-benzofuranyl)-(6-nitro-2-pyridinyl)](methyl)carbamate | 1211333-20-8

中文名称
——
中文别名
——
英文名称
tert-butyl [5-(5-(ethoxymethoxy)-2-benzofuranyl)-(6-nitro-2-pyridinyl)](methyl)carbamate
英文别名
[5-(5-ethoxymethoxy-benzofuran-2-yl)-6-nitro-pyridin-2-yl]-methyl-carbamic acid tert-butyl ester;([5-(5-Ethoxymethoxy-benzofuran-2-yl)-6-nitro-pyridin-2-yl]-methyl-carbamic acid tert-butyl ester);tert-butyl N-[5-[5-(ethoxymethoxy)-1-benzofuran-2-yl]-6-nitropyridin-2-yl]-N-methylcarbamate
tert-butyl [5-(5-(ethoxymethoxy)-2-benzofuranyl)-(6-nitro-2-pyridinyl)](methyl)carbamate化学式
CAS
1211333-20-8
化学式
C22H25N3O7
mdl
——
分子量
443.456
InChiKey
YDLUIXGYKWYMMC-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:
    593.4±50.0 °C(Predicted)
  • 密度:
    1.275±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    32
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    120
  • 氢给体数:
    0
  • 氢受体数:
    8

制备方法与用途

[AZD4694前体][18F]AZD4694是一种用于合成[18F]AZD4694的化合物,后者是一种用于成像淀粉样β斑块的配体,并对淀粉样β斑块具有高度亲和力。

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Compounds Suitable As Precursors to Compounds that are Useful for Imaging Amyloid Deposits
    申请人:Bjõrk Seth
    公开号:US20100056796A1
    公开(公告)日:2010-03-04
    The present invention relates to novel derivatives that are suitable as precursors to compounds that are useful for imaging amyloid deposits in living patients, their compositions, methods of use and processes to make such compounds. The compounds deriving from these precursors are useful in methods of imaging amyloid deposits in brain in vivo to allow antemortem diagnosis of Alzheimer's disease by positron emission tomography (PET) as well as measuring clinical efficacy of Alzheimer's disease therapeutic agents. Furthermore, the present invention also discloses the precursor compounds in crystalline form.
    本发明涉及新型衍生物,适用于成为有用于在活体患者中成像淀粉样沉积的化合物的前体,以及它们的组成、使用方法和制造这些化合物的过程。从这些前体衍生的化合物在体内成像淀粉样沉积的方法中非常有用,以允许通过正电子发射断层扫描(PET)进行临床前诊断阿尔茨海默病,并测量阿尔茨海默病治疗药物的临床疗效。此外,本发明还披露了晶体形式的前体化合物。
  • Compounds suitable as precursors to compounds that are useful for imaging amyloid deposits
    申请人:AstraZeneca AB
    公开号:US08193363B2
    公开(公告)日:2012-06-05
    The present invention relates to novel derivatives that are suitable as precursors to compounds that are useful for imaging amyloid deposits in living patients, their compositions, methods of use and processes to make such compounds. The compounds deriving from these precursors are useful in methods of imaging amyloid deposits in brain in vivo to allow antemortem diagnosis of Alzheimer's disease by positron emission tomography (PET) as well as measuring clinical efficacy of Alzheimer's disease therapeutic agents. Furthermore, the present invention also discloses the precursor compounds in crystalline form.
    本发明涉及新型衍生物,适用于成像活体患者中淀粉样沉积物的化合物的前体,以及它们的组成、使用方法和制备这种化合物的过程。从这些前体衍生的化合物在体内成像淀粉样沉积物的方法中非常有用,可以通过正电子发射断层扫描(PET)进行阿尔茨海默病的临床前诊断,以及测量阿尔茨海默病治疗药物的临床疗效。此外,本发明还披露了晶体形式的前体化合物。
  • COMPOUNDS SUITABLE AS PRECURSORS TO COMPOUNDS THAT ARE USEFUL FOR IMAGING AMYLOID DEPOSITS
    申请人:AstraZeneca AB
    公开号:US20140296534A1
    公开(公告)日:2014-10-02
    The present invention relates to novel derivatives that are suitable as precursors to compounds that are useful for imaging amyloid deposits in living patients, their compositions, methods of use and processes to make such compounds. The compounds deriving from these precursors are useful in methods of imaging amyloid deposits in brain in vivo to allow antemortem diagnosis of Alzheimer's disease by positron emission tomography (PET) as well as measuring clinical efficacy of Alzheimer's disease therapeutic agents. Furthermore, the present invention also discloses the precursor compounds in crystalline form.
    本发明涉及新型衍生物,适用于成为有用于成像活体患者中淀粉样沉积物的化合物的前体,以及它们的组成、使用方法和制备这种化合物的过程。从这些前体衍生的化合物在体内成像淀粉样沉积物的方法中非常有用,可以通过正电子发射断层扫描(PET)进行抗死前诊断阿尔茨海默病,以及测量阿尔茨海默病治疗剂的临床疗效。此外,本发明还揭示了晶体形式的前体化合物。
  • Synthesis and evaluation of pyridylbenzofuran, pyridylbenzothiazole and pyridylbenzoxazole derivatives as 18F-PET imaging agents for β-amyloid plaques
    作者:Britt-Marie Swahn、Johan Sandell、David Pyring、Margareta Bergh、Fredrik Jeppsson、Anders Juréus、Jan Neelissen、Peter Johnström、Magnus Schou、Samuel Svensson
    DOI:10.1016/j.bmcl.2012.05.011
    日期:2012.7
    The synthesis and SAR of new beta-amyloid binding agents are reported. Evaluation of important properties for achieving good signal-to-background ratio is described. Compounds 27, 33, and 36 displayed desirable lipophilic and pharmacokinetic properties. Compound 27 was further evaluated with autoradiographic studies in vitro on human brain tissue and in vivo in Tg2576 mice. Compound 27 showed an increased signal-to-background ratio compared to flutemetamol 4, indicating its suitability as PET ligand for b-amyloid deposits in AD patients. The preparation of the corresponding F-18-labeled PET radioligand of compound 27 is presented. (C) 2012 Elsevier Ltd. All rights reserved.
  • NEW BENZOFURANS SUITABLE AS PRECURSORS TO COMPOUNDS THAT ARE USEFUL FOR IMAGING AMYLOID DEPOSITS
    申请人:AstraZeneca AB
    公开号:EP2328891A1
    公开(公告)日:2011-06-08
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