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2-(3-甲氧基吡啶-2-基)乙醇 | 90087-19-7

中文名称
2-(3-甲氧基吡啶-2-基)乙醇
中文别名
——
英文名称
2-(2-Hydroxy-ethyl>-3-methoxy-pyridin
英文别名
2-(3-methoxy-pyridin-2-yl)-ethanol;2-(3-Methoxypyridin-2-YL)ethanol
2-(3-甲氧基吡啶-2-基)乙醇化学式
CAS
90087-19-7
化学式
C8H11NO2
mdl
——
分子量
153.181
InChiKey
MZBQVMSHCQRSQQ-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):
    0.4
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    42.4
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • [EN] KRAS G12D INHIBITORS<br/>[FR] INHIBITEURS DE KRAS G12D
    申请人:MIRATI THERAPEUTICS INC
    公开号:WO2021041671A1
    公开(公告)日:2021-03-04
    The present invention relates to compounds that inhibit KRas G12D. In particular, the present invention relates to compounds that inhibit the activity of KRas G12D, pharmaceutical compositions comprising the compounds and methods of use therefor.
    本发明涉及抑制KRas G12D的化合物。具体地,本发明涉及抑制KRas G12D活性的化合物,包括这些化合物的药物组合物以及使用方法。
  • 2-CARBOXAMIDE-7-PIPERAZINYL-BENZOFURAN DERIVATIVES 774
    申请人:ANDERSSON Johan
    公开号:US20100331341A1
    公开(公告)日:2010-12-30
    The present invention relates to compounds of formula (I), wherein R 1 is heteroaryl or heterocyclyl, optionally substituted; R 2 is C 1-4 alkyl, heterocyclyl, C 1-4 alkylaryl, C 1-4 alkylheteroaryl, carbocyclyl, C 1-4 alkylheterocyclyl, heterocyclyl-heteroaryl, aryl-heterocyclyl, carbocyclyl-heteroaryl, heterocyclyl-aryl, optionally substituted; R 3 is hydrogen or C 1-4 alkyl, or R 2 and R 3 may together with the nitrogen atom, form a saturated ring system containing 4, 5 or 6 ring forming atoms, and optionally substituted; R 4 is hydrogen, halogen, methyl or methoxy; to pharmaceutical composition containing said compounds and to the use of said compounds in therapy, for instance in treating cognitive disorders. The present invention further relates to new intermediates useful in the preparation thereof.
    本发明涉及公式(I)的化合物,其中R1是杂环芳基或杂环烷基,可选择性取代;R2是C1-4烷基,杂环烷基,C1-4烷基芳基,C1-4烷基杂环芳基,环烷基,C1-4烷基杂环烷基,杂环烷基-杂环芳基,芳基-杂环烷基,环烷基-杂环芳基,杂环烷基-芳基,可选择性取代;R3是或C1-4烷基,或R2和R3可以与原子一起形成含有4、5或6个环形成原子的饱和环系统,并可选择性取代;R4是,卤素,甲基或甲基;含有所述化合物的药物组合物以及所述化合物在治疗中的使用,例如用于治疗认知障碍。本发明还涉及制备中间体的新方法。
  • 2-Carboxamide-7-Piperazinyl-Benzofuran Derivatives
    申请人:ASTRAZENECA AB
    公开号:US20130296296A1
    公开(公告)日:2013-11-07
    The present invention relates to compounds of formula (I), wherein R 1 is heteroaryl or heterocyclyl, optionally substituted; R 2 is C 1-4 alkyl, heterocyclyl, C 1-4 alkylaryl, C 1-4 alkylheteroaryl, carbocyclyl, C 1-4 alkylheterocyclyl, heterocyclyl-heteroaryl, aryl-heterocyclyl, carbocyclyl-heteroaryl, heterocyclyl-aryl, optionally substituted; R 3 is hydrogen or C 1-4 alkyl, or R 2 and R 3 may together with the nitrogen atom, form a saturated ring system containing 4, 5 or 6 ring forming atoms, and optionally substituted; R 4 is hydrogen, halogen, methyl or methoxy; to pharmaceutical composition containing said compounds and to the use of said compounds in therapy, for instance in treating cognitive disorders. The present invention further relates to new intermediates useful in the preparation thereof.
    本发明涉及式(I)的化合物,其中R1是杂环芳基或杂环基,可选地被取代;R2是C1-4烷基,杂环基,C1-4烷基芳基,C1-4烷基杂环芳基,环基,C1-4烷基杂环基,杂环基-杂环芳基,芳基-杂环基,环基-杂环芳基,杂环基-芳基,可选地被取代;R3是或C1-4烷基,或R2和R3可以与原子一起形成4、5或6个环形成原子的饱和环系统,可选地被取代;R4是、卤素、甲基或甲基;以及含有所述化合物的制药组合物和所述化合物在治疗中的用途,例如用于治疗认知障碍。本发明还涉及在其制备中有用的新中间体
  • 2-CARBOXAMIDE-7-PIPERAZINYL-BENZOFURAN DERIVATIVES
    申请人:AstraZeneca AB
    公开号:EP2448934B1
    公开(公告)日:2014-05-21
  • KRAS G12D INHIBITORS
    申请人:Mirati Therapeutics, Inc.
    公开号:EP4021444A1
    公开(公告)日:2022-07-06
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