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5-[(5-bromopentyl)oxy]pent-1-yne | 452340-26-0

中文名称
——
中文别名
——
英文名称
5-[(5-bromopentyl)oxy]pent-1-yne
英文别名
1-Bromo-5-pent-4-ynoxypentane
5-[(5-bromopentyl)oxy]pent-1-yne化学式
CAS
452340-26-0
化学式
C10H17BrO
mdl
——
分子量
233.148
InChiKey
OBEVDZYJLFAPHA-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:
    266.2±25.0 °C(Predicted)
  • 密度:
    1.184±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    12
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and Structure−Activity Relationships of Long-acting β2 Adrenergic Receptor Agonists Incorporating Arylsulfonamide Groups
    摘要:
    A series of saligenin alkoxyalkylphenylsulfonamide beta(2) adrenoceptor agonists were prepared by reacting a protected saligenin oxazolidinone with alkynyloxyalkyl bromides, followed by Sonogashira reaction, hydrogenation, and deprotection. The meta-substituted primary sulfonamide was more potent than the para and the ortho-analogues. Primary sulfonamides were more potent than the secondary and tertiary analogues. The onset and duration of action in vitro of selected compounds was assessed on isolated superfused guinea pig trachea. Sulfonamide 29b had the best profile of potency, selectivity, onset, and duration of action on both guinea pig trachea and human bronchus. Furthermore, 29b was found to have low oral bioavailability in rat and dog and also to have long duration of action in an in vivo model of bronchodilation. Crystalline salts of 29b were identified that had suitable properties for inhaled administration. A proposed binding mode for 29b to the beta(2)-receptor is presented.
    DOI:
    10.1021/jm801016j
  • 作为产物:
    描述:
    1,5-二溴戊烷4-戊炔-1-醇四丁基硫酸氢铵 、 sodium hydroxide 作用下, 以 为溶剂, 反应 72.0h, 生成 5-[(5-bromopentyl)oxy]pent-1-yne
    参考文献:
    名称:
    Synthesis and Structure−Activity Relationships of Long-acting β2 Adrenergic Receptor Agonists Incorporating Arylsulfonamide Groups
    摘要:
    A series of saligenin alkoxyalkylphenylsulfonamide beta(2) adrenoceptor agonists were prepared by reacting a protected saligenin oxazolidinone with alkynyloxyalkyl bromides, followed by Sonogashira reaction, hydrogenation, and deprotection. The meta-substituted primary sulfonamide was more potent than the para and the ortho-analogues. Primary sulfonamides were more potent than the secondary and tertiary analogues. The onset and duration of action in vitro of selected compounds was assessed on isolated superfused guinea pig trachea. Sulfonamide 29b had the best profile of potency, selectivity, onset, and duration of action on both guinea pig trachea and human bronchus. Furthermore, 29b was found to have low oral bioavailability in rat and dog and also to have long duration of action in an in vivo model of bronchodilation. Crystalline salts of 29b were identified that had suitable properties for inhaled administration. A proposed binding mode for 29b to the beta(2)-receptor is presented.
    DOI:
    10.1021/jm801016j
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文献信息

  • Agonists of beta-adrenoceptors
    申请人:——
    公开号:US20040242890A1
    公开(公告)日:2004-12-02
    The present invention relates to novel compounds of formula (I), to a process for their manufacture, to pharmaceutical compositions containing them, and to their use in therapy, in particular their use in the prophylaxis and treatment of respiratory diseases. 1
    本发明涉及公式(I)的新化合物,其制造方法,包含它们的制药组合物以及它们在治疗中的应用,特别是在呼吸系统疾病的预防和治疗中的应用。
  • Phenethanolamine derivatives for treatment of respiratory diseases
    申请人:——
    公开号:US20040180876A1
    公开(公告)日:2004-09-16
    The present invention relates to novel compounds of Formula (I), to a process for their manufacture, to pharmaceutical compositions containing them, and to their use in therapy, in particular their use in the prophylaxis and treatment of respiratory diseases.
    本发明涉及一种新型化合物(I)、其制造方法、包含它们的药物组合物以及它们在治疗中的应用,特别是在呼吸系统疾病的预防和治疗中的应用。
  • PHENETHANOLAMINE DERIVATIVES FOR TREATMENT OF RESPIRATORY DISEASES
    申请人:BIGGADIKE Keith
    公开号:US20060287286A1
    公开(公告)日:2006-12-21
    The present invention relates to novel compounds of Formula (I), to a process for their manufacture, to pharmaceutical compositions containing them, and to their use in therapy, in particular their use in the prophylaxis and treatment of respiratory diseases.
    本发明涉及式(I)的新化合物、其制备方法、含有它们的制药组合物以及它们在治疗中的应用,特别是它们在预防和治疗呼吸系统疾病中的应用。
  • Methods using phenethanolamine derivatives for treatment of respiratory diseases
    申请人:Biggadike Keith
    公开号:US20070004807A1
    公开(公告)日:2007-01-04
    The present invention relates to novel compounds of Formula (I), to a process for their manufacture, to pharmaceutical compositions containing them, and to their use in therapy, in particular their use in the prophylaxis and treatment of respiratory diseases.
    本发明涉及式(I)的新化合物、其制造方法、含有它们的药物组合物,以及它们在治疗中的应用,特别是在呼吸系统疾病的预防和治疗中的应用。
  • AGONISTS OF BETA-ADRENORECEPTORS
    申请人:GLAXO GROUP LIMITED
    公开号:EP1366025B1
    公开(公告)日:2007-06-27
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