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1-(2,4-二氯苯基)-5-(4-羟基苯基)-4-甲基-1H-吡唑-3-羧酸 | 501426-61-5

中文名称
1-(2,4-二氯苯基)-5-(4-羟基苯基)-4-甲基-1H-吡唑-3-羧酸
中文别名
——
英文名称
1-(2,4-dichlorophenyl)-5-(4-hydroxyphenyl)-4-methyl-1H-pyrazole-3-carboxylic acid
英文别名
1-(2,4-dichloro-phenyl)-5-(4-hydroxyphenyl)-4-methyl-1H-pyrazole-3-carboxylic acid;1-(2,4-dichlorophenyl)-5-(4-hydroxyphenyl)-4-methylpyrazole-3-carboxylic acid
1-(2,4-二氯苯基)-5-(4-羟基苯基)-4-甲基-1H-吡唑-3-羧酸化学式
CAS
501426-61-5
化学式
C17H12Cl2N2O3
mdl
——
分子量
363.2
InChiKey
SKDFIUKEZBOAAC-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

  • 熔点:
    >260 °C
  • 沸点:
    569.2±50.0 °C(Predicted)
  • 密度:
    1.47±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.7
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    75.4
  • 氢给体数:
    2
  • 氢受体数:
    4

SDS

SDS:a10fffd14658b51674232631efa1dba1
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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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Pyrazole Derivatives as Cb1 Modulators
    申请人:Cheng Leifeng
    公开号:US20080287517A1
    公开(公告)日:2008-11-20
    The present invention relates to compounds of formula I wherein R 1 represents a group R 5 O— in which R 5 represents a C 3-7 alkyl group substituted by one or more fluoro or R 5 represents a C 3-7 alkylsulphonyl group which is optionally substituted by one or more fluoro; R 2 represents a C 1-4 alkyl group, hydroxy, fluoro, chloro or cyano wherein each R 2 is independently selected when n is >1; R 3 represents a) cyclohexyl optionally substituted by one or more of the following: hydroxy, fluoro, amino, mono or diC 1-3 alkylamino, carboxy or a C 1-4 alkoxycarbonyl group b) piperidino substituted by one or more hydroxy c) unsubstituted piperidino but only when one of the following applies: R 4 represents cyano or R 1 represents 3-fluoropropylsulphonyloxy or R 1 represents 3,3,3-trifluoropropoxy or R 1 represents 3-fluoropropoxy or R 2 is methyl d) phenyl substituted by one or more of the following: hydroxy, halo or a C 1-4 alkyl group e) pyridyl substituted by a C 1-4 alkyl group or f) a C 4-9 alkyl group; R 4 represents cyano or methyl; and n is 1, 2 or 3 and pharmaceutically acceptable salts thereof and processes for preparing such compounds, their use in the treatment of obesity, psychiatric and neurological disorders, to methods for their therapeutic use and to pharmaceutical compositions containing them.
    本发明涉及一种式I的化合物,其中R1表示R5O-基团,其中R5表示一个C3-7烷基基团,该基团被一个或多个代或R5表示一个C3-7烷基磺酰基团,该基团可被一个或多个代取代;R2表示C1-4烷基基团,羟基,,其中当n>1时,每个R2是独立选择的;R3表示a)环己基,可选地被以下一种或多种取代:羟基,基,单或双C1-3烷基基,羧基或C1-4烷氧羰基基团b)哌啶取代的羟基或多个羟基c)未取代的哌啶,但仅当以下之一适用时:R4表示基或R1表示3-丙基磺酰氧基或R1表示3,3,3-三丙氧基或R1表示3-丙氧基或R2为甲基d)苯基,可选地被以下一种或多种取代:羟基,卤素或C1-4烷基基团e)吡啶基,取代为C1-4烷基基团或f)C4-9烷基基团;R4表示基或甲基;n为1、2或3,以及其药学上可接受的盐和制备这种化合物的过程,它们在肥胖症、精神和神经疾病的治疗中的用途,以及它们的治疗用途的方法和包含它们的制药组合物。
  • Therapeutic Agents
    申请人:Cheng Leifeng
    公开号:US20080146614A1
    公开(公告)日:2008-06-19
    The present invention relates to 1,5-diphenylpyrazole compounds of formula I (A chemical formula should be inserted here—please see paper copy enclosed herewith) and processes for preparing such compounds, their use in the treatment of obesity, psychiatric and neurological disorders, to methods for their therapeutic use and to pharmaceutical compositions containing them.
    本发明涉及式I的1,5-二苯基吡唑化合物(化学式应在此处插入-请参见随附的纸质副本)以及制备这些化合物的过程,它们在肥胖症、精神和神经疾病的治疗中的应用,以及它们的治疗应用方法和含有它们的制药组合物。
  • THERAPEUTIC AGENTS
    申请人:Cheng Leifeng
    公开号:US20100234439A1
    公开(公告)日:2010-09-16
    The present invention relates to a 1,5-diphenylpyrazole compound and its use in the treatment of obesity, psychiatric and neurological disorders, to methods for the its therapeutic use and to pharmaceutical compositions containing them.
    本发明涉及一种1,5-二苯基吡唑化合物及其在肥胖症、精神和神经疾病治疗中的应用,以及其治疗应用的方法和包含它们的制药组合物。
  • WO2007/148062
    申请人:——
    公开号:——
    公开(公告)日:——
  • Synthesis, Structure−Activity Relationship, and Evaluation of SR141716 Analogues:  Development of Central Cannabinoid Receptor Ligands with Lower Lipophilicity
    作者:Reeti Katoch-Rouse、Olga A. Pavlova、Tara Caulder、Alexander F. Hoffman、Alexey G. Mukhin、Andrew G. Horti
    DOI:10.1021/jm020157x
    日期:2003.2.1
    Exploration of the central CB1 cannabinoid receptors using positron emission tomography (PET) will allow for an understanding of the pharmacological and physiological role played by these receptors in the CNS. Current tracers are highly lipophilic compounds that exhibit very high nonspecific to specific binding ratios and as a result are inapt for use in humans. We have synthesized a series of less lipophilic analogues of SR141716 to serve as potential radioligands. Binding affinities of the series and a functional electrophysiological assay of three of our compounds have been presented.
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