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5-{4-[6-fluoro-1-(2-thiophen-3-yl-ethyl)-1H-indol-3-yl]-piperidin-1-ylmethyl}-2-methoxy-benzoic acid | 423173-22-2

中文名称
——
中文别名
——
英文名称
5-{4-[6-fluoro-1-(2-thiophen-3-yl-ethyl)-1H-indol-3-yl]-piperidin-1-ylmethyl}-2-methoxy-benzoic acid
英文别名
5-[[4-[6-Fluoro-1-(2-thiophen-3-ylethyl)indol-3-yl]piperidin-1-yl]methyl]-2-methoxybenzoic acid
5-{4-[6-fluoro-1-(2-thiophen-3-yl-ethyl)-1H-indol-3-yl]-piperidin-1-ylmethyl}-2-methoxy-benzoic acid化学式
CAS
423173-22-2
化学式
C28H29FN2O3S
mdl
——
分子量
492.614
InChiKey
HUYSKCNNHCZXOK-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):
    3
  • 重原子数:
    35
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    82.9
  • 氢给体数:
    1
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    6-fluoro-3-piperidin-4-yl-1-(2-thiophen-3-yl-ethyl)-1H-indoleethyl 3-(bromomethyl)-4-methoxybenzoate 以29%的产率得到5-{4-[6-fluoro-1-(2-thiophen-3-yl-ethyl)-1H-indol-3-yl]-piperidin-1-ylmethyl}-2-methoxy-benzoic acid
    参考文献:
    名称:
    Indolylpiperidine derivatives as antihistaminic aand antiallergic agents
    摘要:
    该发明涉及式(I)的吲哚基哌啶衍生物,其中:A1代表烷基、烷氧基、硫代烷基、烷酰基或羟基烷基基团;A2代表烷基、烷氧基、硫代烷基、烷酰基或烷氧基烷基基团;W1代表苯基、呋喃基或吡啶基,该基团未取代或被一个或多个卤素原子、烷氧基和/或烷基取代;W2代表含有1至3个杂原子的3-10元成员的单环或双环基团,该基团未取代或被一个或多个卤素原子、烷基、烷氧基和/或氧代基取代;R1代表氢原子或卤素原子或烷基、烷氧基或甲氧基氨基基团;R2代表羧基;及其药学上可接受的盐;其制备方法;含有它们的药物组合物;以及它们作为抗组胺和抗过敏药物的医药用途。
    公开号:
    US20040116471A1
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文献信息

  • INDOLYLPIPERIDINE DERIVATIVES AS ANTIHISTAMINIC AND ANTIALLERGIC AGENTS
    申请人:Almirall Prodesfarma, S.A.
    公开号:EP1330453B1
    公开(公告)日:2006-03-29
  • US7189741B2
    申请人:——
    公开号:US7189741B2
    公开(公告)日:2007-03-13
  • [EN] INDOLYLPIPERIDINE DERIVATIVES AS ANTIHISTAMINIC AND ANTIALLERGIC AGENTS<br/>[FR] DERIVES D'INDOLYLPIPERIDINE UTILISES COMME AGENTS ANTIHISTAMINIQUES ET ANTIALLERGIQUES
    申请人:ALMIRALL PRODESFARMA SA
    公开号:WO2002036589A1
    公开(公告)日:2002-05-10
    The invention relates to indolyl piperidinyl derivatives of formula (I) wherein: A1 represents an alkylene, alkyleneoxy, alkylenethio, alkanoylene or hydroxyalkylene group; A2 represents an alkylene, alkyleneoxy, alkylenethio, alkanoylene or an alkyleneoxyalkylene group; W1 represents a phenylene, furanylene or pyridinylene group which is unsubstituted or substituted by one or more halogen atoms, alkoxy groups and/or alkyl groups; W2 represents a 3-10 membered monocyclic or bicyclic group containing from 1 to 3 heteroatoms said group being unsubstituted or substituted by one or more halogen atoms, alkyl groups, alkoxy groups and/or oxo groups; R1 represents a hydrogen or halogen atom or an alkyl, alkoxy or methylamino group; and R2 represents a carboxyl group; and pharmaceutically acceptable salts thereof; to processes for their preparation; to pharmaceutical compositions containing them; and to their medical use as antihistaminic and antiallergic agents.
  • Indolylpiperidine derivatives as antihistaminic aand antiallergic agents
    申请人:——
    公开号:US20040116471A1
    公开(公告)日:2004-06-17
    The invention relates to indolyl piperidinyl derivatives of formula (I) wherein: A 1 represents an alkylene, alkyleneoxy, alkylenethio, alkanoylene or hydroxyalkylene group; A 2 represents an alkylene, alkyleneoxy, alkylenethio, alkanoylene or an alkyleneoxyalkylene group; W 1 represents a phenylene, furanylene or pyridinylene group which is unsubstituted or substituted by one or more halogen atoms, alkoxy groups and/or alkyl groups; W 2 represents a 3-10 membered monocyclic or bicyclic group containing from 1 to 3 heteroatoms said group being unsubstituted or substituted by one or more halogen atoms, alkyl groups, alkoxy groups and/or oxo groups; R 1 represents a hydrogen or halogen atom or an alkyl, alkoxy or methylamino group; and R 2 represents a carboxyl group; and pharmaceutically acceptable salts thereof; to processes for their preparation; to pharmaceutical compositions containing them; and to their medical use as antihistaminic and antiallergic agents.
    该发明涉及式(I)的吲哚基哌啶衍生物,其中:A1代表烷基、烷氧基、硫代烷基、烷酰基或羟基烷基基团;A2代表烷基、烷氧基、硫代烷基、烷酰基或烷氧基烷基基团;W1代表苯基、呋喃基或吡啶基,该基团未取代或被一个或多个卤素原子、烷氧基和/或烷基取代;W2代表含有1至3个杂原子的3-10元成员的单环或双环基团,该基团未取代或被一个或多个卤素原子、烷基、烷氧基和/或氧代基取代;R1代表氢原子或卤素原子或烷基、烷氧基或甲氧基氨基基团;R2代表羧基;及其药学上可接受的盐;其制备方法;含有它们的药物组合物;以及它们作为抗组胺和抗过敏药物的医药用途。
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