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2-(5-溴吡啶-2-基氧基)乙酸甲酯 | 845890-35-9

中文名称
2-(5-溴吡啶-2-基氧基)乙酸甲酯
中文别名
2-[(5-溴-2-吡啶基)氧基]乙酸甲酯
英文名称
methyl 2-((5-bromopyridin-2-yl)oxy)acetate
英文别名
methyl [(5-bromo-2-pyridinyl)oxy]acetate;Methyl 2-[(5-Bromo-2-pyridyl)oxy]acetate;methyl 2-(5-bromopyridin-2-yl)oxyacetate
2-(5-溴吡啶-2-基氧基)乙酸甲酯化学式
CAS
845890-35-9
化学式
C8H8BrNO3
mdl
——
分子量
246.06
InChiKey
LRXINRZZHRWYRF-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:
    278.0±25.0 °C(Predicted)
  • 密度:
    1.544±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    48.4
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2,5-二溴吡啶羟乙酸甲酯 在 sodium hydride 、 盐酸 作用下, 以 DMF (N,N-dimethyl-formamide) 、 mineral oil 为溶剂, 反应 16.0h, 以73%的产率得到2-(5-溴吡啶-2-基氧基)乙酸甲酯
    参考文献:
    名称:
    [EN] 2-SUBSTITUTED BENZOIC ACID DERIVATIVES AS HM74A RECEPTOR AGONISTS
    [FR] DERIVES D'ACIDE BENZOIQUE 2-SUBSTITUE EN TANT QU'AGONISTE DU RECEPTEUR HM74A
    摘要:
    公开了具有以下式(I)中定义的R1、R2和Z的治疗活性的邻氨基苯甲酸衍生物,制备所述衍生物的方法,含有活性化合物的药物配方以及化合物在治疗中的用途,特别是在HM74A受体的低活化导致疾病或激活受体将有益的疾病的治疗中。
    公开号:
    WO2005016870A1
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文献信息

  • [EN] 4-(2-FLUORO-4-METHOXY-5-3-(((1-METHYLCYCLOBUTYL)METHYL)CARBAMOYL)BICYCLO[2.2.1]HEPTAN-2-YL)CARBAMOYL)PHENOXY)-1-METHYLCYCLOHEXANE-1-CARBOXYLIC ACID DERIVATIVES AND SIMILAR COMPOUNDS AS RXFP1 MODULATORS FOR THE TREATMENT OF HEART FAILURE<br/>[FR] DÉRIVÉS D'ACIDE 4-(2-FLUORO-4-MÉTHOXY-5-3-(((1-MÉTHYLCYCLOBUTYLE)MÉTHYL)CARBAMOYL)BICYCLO[2.2.1]HEPTAN-2-YL) CARBAMOYL)PHÉNOXY)-1-MÉTHYLCYCLOHEXANE-1-CARBOXYLIQUE ET COMPOSÉS SIMILAIRES COMME MODULATEURS DE RXFP1 POUR LE TRAITEMENT DE L'INSUFFISANCE CARDIAQUE
    申请人:ASTRAZENECA AB
    公开号:WO2022122773A1
    公开(公告)日:2022-06-16
    The present invention relates to 4-(2-Fluoro-4-methoxy-5-3-(((l- methylcyclobutyl)methyl)carbamoyl)bicyclo[2.2.1]heptan-2-yl) carbamoyl)phenoxy)-l-methylcyclohexane-l-carboxylic acid derivatives and similar compounds of formula (I) as RXFP1 modulators for the treatment of heart failure, heart failure with preserved ejection fraction, heart failure with mid-range ejection fraction, heart failure with reduced ejection fraction, chronic kidney disease and acute kidney injury. The present invention also relates to crystalline forms of such compounds. An exemplary compound is e.g. (A).
    本发明涉及4-(2-氟-4-甲氧基-5-3-(((1-甲基环丁基)甲基)氨基)双环[2.2.1]庚烷-2-基)氨基苯氧基)-1-甲基环己烷-1-羧酸衍生物及类似化合物,其为RXFP1调节剂,用于治疗心力衰竭、保留射血分数的心力衰竭、中等射血分数的心力衰竭、降低射血分数的心力衰竭、慢性肾脏病和急性肾损伤。本发明还涉及这种化合物的晶体形式。一个示例化合物是例如(A)。
  • Organic compounds
    申请人:Novartis AG
    公开号:EP2177518A1
    公开(公告)日:2010-04-21
    3,4-substituted piperidine compounds, these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (= disorder) that depends on activity of renin; the use of a compound of that class for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; pharmaceutical formulations comprising a 3,4-substituted piperidine compound, and/or a method of treatment comprising administering a 3,4-substituted piperidine compound, a method for the manufacture of a 3,4-substituted piperidine compound, and novel intermediates and partial steps for their synthesis are disclosed. The 3,4-disubstituted piperidine compounds have the formula I, wherein the symbols have the meanings defined in the specification.
    3,4-取代的哌啶化合物,这些化合物用于温血动物的诊断和治疗,特别是用于治疗依赖于肾素活性的疾病(=失调);该类化合物用于制备治疗依赖于肾素活性的疾病的药物制剂;公开了该类化合物在治疗依赖肾素活性的疾病中的用途;包含3,4-取代的哌啶化合物的药物制剂,和/或包括施用3,4-取代的哌啶化合物的治疗方法,3,4-取代的哌啶化合物的制造方法,以及新型中间体及其合成的部分步骤。3,4-二取代哌啶化合物具有式 I、 其中符号具有本说明书中定义的含义。
  • SUBSTITUTED PIPERIDINES AS RENIN INHIBITORS
    申请人:Novartis AG
    公开号:EP1833816A1
    公开(公告)日:2007-09-19
  • ORGANIC COMPOUNDS
    申请人:Breitenstein Werner
    公开号:US20090312304A1
    公开(公告)日:2009-12-17
    3,4-substituted piperidine compounds, these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; the use of a compound of that class for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; pharmaceutical formulations comprising a 3,4-substituted piperidine compound, and/or a method of treatment comprising administering a 3,4-substituted piperidine compound, a method for the manufacture of a 3,4-substituted piperidine compound, and novel intermediates and partial steps for their synthesis are disclosed. The 3,4-disubstituted piperidine compounds have the formula I,
  • Organic Compounds
    申请人:BREITENSTEIN Werner
    公开号:US20110263560A1
    公开(公告)日:2011-10-27
    3,4-substituted piperidine compounds, these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; the use of a compound of that class for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; pharmaceutical formulations comprising a 3,4-substituted piperidine compound, and/or a method of treatment comprising administering a 3,4substituted piperidine compound, a method for the manufacture of a 3,4-substituted piperidine compound, and novel intermediates and partial steps for their synthesis are disclosed. The 3,4-disubstituted piperidine compounds have the formula (I), wherein the symbols have the meanings defined in the specification.
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