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6-氟-2-甲基-喹啉-3-羧酸 | 461026-47-1

中文名称
6-氟-2-甲基-喹啉-3-羧酸
中文别名
——
英文名称
6-Fluoro-2-methylquinoline-3-carboxylic acid
英文别名
——
6-氟-2-甲基-喹啉-3-羧酸化学式
CAS
461026-47-1
化学式
C11H8FNO2
mdl
MFCD03085774
分子量
205.18
InChiKey
ZPRUQEILFHQVHS-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):
    2.2
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    50.2
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 危险性防范说明:
    P261,P264,P270,P271,P280,P301+P312,P302+P352,P304+P340,P305+P351+P338,P330,P332+P313,P337+P313,P362,P403+P233,P405,P501
  • 危险性描述:
    H302,H315,H319,H335

反应信息

  • 作为反应物:
    描述:
    2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)phenylamine6-氟-2-甲基-喹啉-3-羧酸 生成 6-fluoro-2-methyl-quinoline-3-carboxylic acid [2-methyl-4-(2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenyl]-amide
    参考文献:
    名称:
    Substituted N-phenyl-bipyrrolidine carboxamides and therapeutic use thereof
    摘要:
    本发明披露和声明了一系列公式(I)的取代N-苯基双吡咯烷羧酰胺化合物。其中R、R1、R2、R3和R4如本文所述。更具体地说,本发明的化合物是H3受体调节剂,因此在治疗和/或预防包括与中枢神经系统相关的多种H3受体调节的疾病中,特别是作为药物剂量,是非常有用的。此外,本发明还披露了取代N-苯基双吡咯烷羧酰胺化合物及其中间体的制备方法。
    公开号:
    US08618159B2
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文献信息

  • [EN] SUBSTITUTED N-PHENYL-BIPYRROLIDINE CARBOXAMIDES AND THERAPEUTIC USE THEREOF<br/>[FR] CARBOXAMIDES DE N-PHÉNYL-BIPYRROLIDINE SUBSTITUÉS ET LEUR UTILISATION THÉRAPEUTIQUE
    申请人:SANOFI AVENTIS
    公开号:WO2009052065A1
    公开(公告)日:2009-04-23
    The present invention discloses and claims a series of substituted N-phenyl-bipyrrolidine carboxamides of formula (I), Wherein R, R1, R2, R3 and R4 are as described herein. More specifically, the compounds of this invention are modulators of H3 receptors and are, therefore, useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of diseases modulated by H3 receptors including diseases associated with the central nervous system. Additionally, this invention also discloses methods of preparation of substituted N-phenyl-bipyrrolidine carboxamides and intermediates therefor.
    本发明公开并声明了一系列式(I)的取代N-苯基-双吡咯烷羧酰胺,其中R、R1、R2、R3和R4如本文所述。更具体地说,本发明的化合物是H3受体调节剂,因此在制药方面特别有用,尤其是在治疗和/或预防通过H3受体调节的各种疾病,包括与中枢神经系统相关的疾病。此外,本发明还公开了取代N-苯基-双吡咯烷羧酰胺及其中间体的制备方法。
  • SUBSTITUTED N-PHENYL-BIPYRROLIDINE CARBOXAMIDES AND THERAPEUTIC USE THEREOF
    申请人:CZECHTIZKY Werngard
    公开号:US20100173897A1
    公开(公告)日:2010-07-08
    The present invention discloses and claims a series of substituted N-phenyl-bipyrrolidine carboxamides of formula (I). Wherein R, R 1 , R 2 , R 3 and R 4 are as described herein. More specifically, the compounds of this invention are modulators of H3 receptors and are, therefore, useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of diseases modulated by H3 receptors including diseases associated with the central nervous system. Additionally, this invention also discloses methods of preparation of substituted N-phenyl-bipyrrolidine carboxamides and intermediates therefor.
    本发明揭示和声明了一系列取代的N-苯基双吡咯烷羧酰胺化合物,其化学式为(I),其中R、R1、R2、R3和R4如本文所述。更具体地,本发明的化合物是H3受体调节剂,因此在治疗和/或预防包括与中枢神经系统相关的多种H3受体调节的疾病方面,特别是作为药物剂量是有用的。此外,本发明还揭示了取代的N-苯基双吡咯烷羧酰胺及其中间体的制备方法。
  • US8618159B2
    申请人:——
    公开号:US8618159B2
    公开(公告)日:2013-12-31
  • Substituted N-phenyl-bipyrrolidine carboxamides and therapeutic use thereof
    申请人:Czechtizky Werngard
    公开号:US08618159B2
    公开(公告)日:2013-12-31
    The present invention discloses and claims a series of substituted N-phenyl-bipyrrolidine carboxamides of formula (I). Wherein R, R1, R2, R3 and R4 are as described herein. More specifically, the compounds of this invention are modulators of H3 receptors and are, therefore, useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of diseases modulated by H3 receptors including diseases associated with the central nervous system. Additionally, this invention also discloses methods of preparation of substituted N-phenyl-bipyrrolidine carboxamides and intermediates therefor.
    本发明披露和声明了一系列公式(I)的取代N-苯基双吡咯烷羧酰胺化合物。其中R、R1、R2、R3和R4如本文所述。更具体地说,本发明的化合物是H3受体调节剂,因此在治疗和/或预防包括与中枢神经系统相关的多种H3受体调节的疾病中,特别是作为药物剂量,是非常有用的。此外,本发明还披露了取代N-苯基双吡咯烷羧酰胺化合物及其中间体的制备方法。
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