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1-(quinolin-2-yl)-1H-pyrrolo[2,3-b]pyridine | 808138-02-5

中文名称
——
中文别名
——
英文名称
1-(quinolin-2-yl)-1H-pyrrolo[2,3-b]pyridine
英文别名
2-pyrrolo[2,3-b]pyridin-1-ylquinoline
1-(quinolin-2-yl)-1H-pyrrolo[2,3-b]pyridine化学式
CAS
808138-02-5
化学式
C16H11N3
mdl
——
分子量
245.283
InChiKey
FVOXXVWYCCZRJP-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:
    450.7±33.0 °C(Predicted)
  • 密度:
    1.24±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    30.7
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-(quinolin-2-yl)-1H-pyrrolo[2,3-b]pyridine三氟乙酸酐碳酸氢钠 、 solid 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 20.0~60.0 ℃ 、359.97 kPa 条件下, 反应 132.0h, 以5.92 g of 3-trifluoroacetyl-1-(quinolin-2-yl)-1H-pyrrolo[2,3-b]pyridine were thus obtained in the form of a brown solid melting at 198° C. which的产率得到3-trifluoroacetyl-1-(quinolin-2-yl)-1H-pyrrolo[2,3-b]pyridine
    参考文献:
    名称:
    Derivatives of 3-(Guanidinocarbonyl) heterocycle, methods of preparation and intermediates thereof, their use as medicaments, and pharmaceutical compositions therefrom
    摘要:
    本发明揭示和声明了式I的化合物及其药学上可接受的盐,并且揭示了使用该式I的化合物,无论是单独使用还是与其他药物联合使用,作为具有心脏保护成分的抗心律失常药物,用于预防或治疗梗死,治疗心绞痛,并作为抑制与缺血引起的损伤发展相关的病理生理过程的药物,特别是在触发缺血诱发的心脏心律失常和心力衰竭方面。还揭示和声明了包含式I化合物或式I化合物与一个或多个其他药物组合的制药组合物,以及制备式I化合物的方法。
    公开号:
    US07230007B2
  • 作为产物:
    描述:
    7-氮杂吲哚2-氯喹啉 在 sodium hydride 作用下, 以 DMF (N,N-dimethyl-formamide) 为溶剂, 反应 15.5h, 生成 1-(quinolin-2-yl)-1H-pyrrolo[2,3-b]pyridine
    参考文献:
    名称:
    [EN] 3-(GUANIDINOCARBONYL)HETEROCYCLE DERIVATIVES, PREPARATION PROCESS AND INTERMEDIATES OF THIS PROCESS, THEIR USE AS MEDICAMENTS, AND PHARMACEUTICAL COMPOSITIONS INCLUDING THEM
    [FR] DERIVES HETEROCYCLIQUES 3-(GUANIDINOCARBONYLE), LEUR PROCEDE DE PREPARATION ET INTERMEDIAIRES POUR LEDIT PROCEDE, LEUR UTILISATION EN TANT QUE MEDICAMENTS ET COMPOSITIONS PHARMACEUTIQUE LES COMPRENANT
    摘要:
    本发明涉及公式(I)的新化合物及其药学上可接受的盐。这些新化合物适用于例如心律失常药物,其具有心脏保护成分,用于预防和治疗心肌梗死以及治疗心绞痛。它们还能预防性地抑制与缺血性损伤发展相关的病理生理过程,特别是在诱发缺血性心律失常和心力衰竭方面。
    公开号:
    WO2004111048A1
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文献信息

  • Derivatives of 3-(guanidinocarbonyl) heterocycle, methods of preparation and intermediates thereof, their use as medicaments, and pharmaceutical compositions therefrom
    申请人:Carry Jean-Christophe
    公开号:US20050014758A1
    公开(公告)日:2005-01-20
    The present invention discloses and claims compounds of formula I and their pharmaceutically acceptable salts, and methods of using said compounds of formula I, either alone or in combination with other medicaments, as antiarrhythmic medicaments with a cardioprotective component for prophylaxis or treatment of infarction, for the treatment of angina pectoris, and as inhibitors of pathophysiological processes associated with the development of ischemia-induced damage, in particular in the triggering of ischemia-induced cardiac arrhythmias and of heart failure. Pharmaceutical compositions comprising compounds of formula I or compounds of formula I in combination with one or more other medicaments and processes for the preparation of compounds of formula I are also disclosed and claimed.
    本发明揭示和声明了I式化合物及其药物可接受的盐,以及使用该I式化合物,单独或与其他药物联合使用,作为具有心脏保护成分的抗心律失常药物,用于预防或治疗梗死,治疗心绞痛,并作为与缺血诱导损伤发展相关的病理生理过程的抑制剂,特别是在诱发缺血诱导的心脏心律失常和心力衰竭方面。本发明还揭示和声明了包括I式化合物或I式化合物与一种或多种其他药物组合的制药组合物,以及制备I式化合物的方法。
  • 3-(GUANIDINOCARBONYL)HETEROCYCLE DERIVATIVES, PREPARATION PROCESS AND INTERMEDIATES OF THIS PROCESS, THEIR USE AS MEDICAMENTS, AND PHARMACEUTICAL COMPOSITIONS INCLUDING THEM
    申请人:Sanofi-Aventis Deutschland GmbH
    公开号:EP1641791A1
    公开(公告)日:2006-04-05
  • US7230007B2
    申请人:——
    公开号:US7230007B2
    公开(公告)日:2007-06-12
  • [EN] 3-(GUANIDINOCARBONYL)HETEROCYCLE DERIVATIVES, PREPARATION PROCESS AND INTERMEDIATES OF THIS PROCESS, THEIR USE AS MEDICAMENTS, AND PHARMACEUTICAL COMPOSITIONS INCLUDING THEM<br/>[FR] DERIVES HETEROCYCLIQUES 3-(GUANIDINOCARBONYLE), LEUR PROCEDE DE PREPARATION ET INTERMEDIAIRES POUR LEDIT PROCEDE, LEUR UTILISATION EN TANT QUE MEDICAMENTS ET COMPOSITIONS PHARMACEUTIQUE LES COMPRENANT
    申请人:AVENTIS PHARMA GMBH
    公开号:WO2004111048A1
    公开(公告)日:2004-12-23
    The present invention relates to the novel compounds of the formula (I) and their pharmaceutically acceptable salts. The inventive compounds are suitable, for example, as antiarrhythmic medicaments with a cardioprotective component for infarction prophylaxis and infarction treatment and for the treatment of angina pectoris. They also inhibit in a preventive manner the pathophysiologicaI processes associated with the development of ischemia-induced damage, in particular in the triggering of ischemia-induced cardiac arrhythmias and of heart failure.
    本发明涉及公式(I)的新化合物及其药学上可接受的盐。这些新化合物适用于例如心律失常药物,其具有心脏保护成分,用于预防和治疗心肌梗死以及治疗心绞痛。它们还能预防性地抑制与缺血性损伤发展相关的病理生理过程,特别是在诱发缺血性心律失常和心力衰竭方面。
  • Derivatives of 3-(Guanidinocarbonyl) heterocycle, methods of preparation and intermediates thereof, their use as medicaments, and pharmaceutical compositions therefrom
    申请人:Sanofi-Aventis Deutschland GmbH
    公开号:US07230007B2
    公开(公告)日:2007-06-12
    The present invention discloses and claims compounds of formula I and their pharmaceutically acceptable salts, and methods of using said compounds of formula I, either alone or in combination with other medicaments, as antiarrhythmic medicaments with a cardioprotective component for prophylaxis or treatment of infarction, for the treatment of angina pectoris, and as inhibitors of pathophysiological processes associated with the development of ischemia-induced damage, in particular in the triggering of ischemia-induced cardiac arrhythmias and of heart failure. Pharmaceutical compositions comprising compounds of formula I or compounds of formula I in combination with one or more other medicaments and processes for the preparation of compounds of formula I are also disclosed and claimed.
    本发明揭示和声明了式I的化合物及其药学上可接受的盐,并且揭示了使用该式I的化合物,无论是单独使用还是与其他药物联合使用,作为具有心脏保护成分的抗心律失常药物,用于预防或治疗梗死,治疗心绞痛,并作为抑制与缺血引起的损伤发展相关的病理生理过程的药物,特别是在触发缺血诱发的心脏心律失常和心力衰竭方面。还揭示和声明了包含式I化合物或式I化合物与一个或多个其他药物组合的制药组合物,以及制备式I化合物的方法。
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