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2-methyl-3-(4-{4-[4-(trifluoromethoxy)phenoxy]piperidin-1-yl}phenoxy)propane-1,2-diol | 1318734-91-6

中文名称
——
中文别名
——
英文名称
2-methyl-3-(4-{4-[4-(trifluoromethoxy)phenoxy]piperidin-1-yl}phenoxy)propane-1,2-diol
英文别名
2-methyl-3-[4-[4-[4-(trifluoromethoxy)phenoxy]piperidin-1-yl]phenoxy]propane-1,2-diol
2-methyl-3-(4-{4-[4-(trifluoromethoxy)phenoxy]piperidin-1-yl}phenoxy)propane-1,2-diol化学式
CAS
1318734-91-6
化学式
C22H26F3NO5
mdl
——
分子量
441.447
InChiKey
HLDIJEYVAMSFEY-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:
    572.4±50.0 °C(Predicted)
  • 密度:
    1.297±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.3
  • 重原子数:
    31
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    71.4
  • 氢给体数:
    2
  • 氢受体数:
    9

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:
    参考文献:
    名称:
    [EN] SYNTHETIC INTERMEDIATE OF OXAZOLE COMPOUND AND METHOD FOR PRODUCING THE SAME
    [FR] INTERMÉDIAIRE SYNTHÉTIQUE D'UN COMPOSÉ OXAZOLE ET PROCÉDÉ DE PRODUCTION ASSOCIÉ
    摘要:
    本发明的目的是提供一种高产率生产噁唑化合物的方法。该目的可以通过由式(11)表示的化合物实现:其中R1是氢原子或较低的烷基基团;R2是在4-位被取代的1-哌啶基团,所述取代基选自(A1a)苯氧基在苯基上取代一个或多个卤素取代的较低烷氧基团,(A1b)苯氧基取代的较低烷基基团在苯基上取代一个或多个卤素取代的较低烷基基团,(A1c)苯基取代的较低烷氧基较低烷基基团在苯基上取代卤素,(A1d)苯基取代的较低烷基基团在苯基上取代一个或多个卤素取代的较低烷氧基团,(A1e)氨基取代的苯基取代一个或多个卤素取代的较低烷氧基团和较低烷基基团,以及(A1f)苯基取代的较低烷氧基团在苯基上取代一个或多个卤素取代的较低烷氧基团;n是1到6之间的整数;X3是有机磺酰氧基团。
    公开号:
    WO2011093529A1
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文献信息

  • SYNTHETIC INTERMEDIATE OF OXAZOLE COMPOUND AND METHOD FOR PRODUCING THE SAME
    申请人:Yamamoto Akihiro
    公开号:US20120302757A1
    公开(公告)日:2012-11-29
    An object of the present invention is to provide a method for producing an oxazole compound in a high yield. The object can be achieved by a compound represented by Formula (11): wherein R 1 is a hydrogen atom or lower-alkyl group; R 2 is a 1-piperidyl group substituted at the 4-position with a substituent selected from (A1a) a phenoxy group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups, (A1b) a phenoxy-substituted lower-alkyl group substituted on the phenyl moiety with one or more halogen-substituted lower-alkyl groups, (A1c) a phenyl-substituted lower-alkoxy lower-alkyl group substituted on the phenyl moiety with halogen, (A1d) a phenyl-substituted lower-alkyl group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups, (A1e) an amino group substituted with a phenyl group substituted with one or more halogen-substituted lower-alkoxy groups, and a lower-alkyl group, and (A1f) a phenyl-substituted lower-alkoxy group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups; n is an integer from 1 to 6; and X 3 is an organic sulfonyloxy group.
    本发明的目的是提供一种高产率制备噁唑化合物的方法。该目的可以通过式(11)表示的化合物实现:其中R1是氢原子或低烷基基团;R2是在4-位被取代的1-哌啶基团,所述取代基被选择自(A1a)在苯基上取代一个或多个卤素取代低烷氧基的苯氧基,(A1b)在苯基上取代一个或多个卤素取代低烷基的苯氧基取代低烷基基团,(A1c)在苯基上取代卤素的苯基取代低烷氧基低烷基基团,(A1d)在苯基上取代一个或多个卤素取代低烷氧基的苯基取代低烷基基团,(A1e)取代有苯基的氨基取代一个或多个卤素取代低烷氧基的苯基和低烷基基团,以及(A1f)在苯基上取代一个或多个卤素取代低烷氧基的苯基取代低烷氧基基团;n是1到6的整数;X3是有机磺酰氧基团。
  • Synthetic intermediate of oxazole compound and method for producing the same
    申请人:Yamamoto Akihiro
    公开号:US08598358B2
    公开(公告)日:2013-12-03
    An object of the present invention is to provide a method for producing an oxazole compound in a high yield. The object can be achieved by a compound represented by Formula (11): wherein R1 is a hydrogen atom or lower-alkyl group; R2 is a 1-piperidyl group substituted at the 4-position with a substituent selected from (A1a) a phenoxy group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups, (A1b) a phenoxy-substituted lower-alkyl group substituted on the phenyl moiety with one or more halogen-substituted lower-alkyl groups, (A1c) a phenyl-substituted lower-alkoxy lower-alkyl group substituted on the phenyl moiety with halogen, (A1d) a phenyl-substituted lower-alkyl group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups, (A1e) an amino group substituted with a phenyl group substituted with one or more halogen-substituted lower-alkoxy groups, and a lower-alkyl group, and (A1f) a phenyl-substituted lower-alkoxy group substituted on the phenyl moiety with one or more halogen-substituted lower-alkoxy groups; n is an integer from 1 to 6; and X3 is an organic sulfonyloxy group.
    本发明的目的是提供一种高产率合成噁唑化合物的方法。该目的可以通过公式(11)所表示的化合物实现:其中,R1是氢原子或低烷基基团;R2是在4位被取代的1-哌啶基团,所述取代基被选择自:(A1a)苯基取代苯基部分上带有一种或多种卤素取代的低烷氧基取代基的苯氧基;(A1b)苯基取代苯基部分上带有一种或多种卤素取代的低烷基取代基的苯氧基取代基;(A1c)苯基取代苯基部分上带有卤素的低烷氧基低烷基取代基的苯基取代基;(A1d)苯基取代苯基部分上带有一种或多种卤素取代的低烷氧基取代基的苯基取代基;(A1e)氨基取代一种带有一种或多种卤素取代的低烷氧基的苯基取代的苯基,以及一种低烷基基团;和(A1f)苯基取代苯基部分上带有一种或多种卤素取代的低烷氧基取代基的苯基取代基。n是1到6的整数;X3是有机磺酰氧基团。
  • METHOD FOR PRODUCING 1-(4-HYDROXYPHENYL)-4-(4-TRIFLUOROMETHOXYPHENOXY)PIPERIDINE OR SALT THEREOF
    申请人:Otsuka Pharmaceutical Co., Ltd.
    公开号:EP3275862A1
    公开(公告)日:2018-01-31
    The present invention provides a method for producing 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine or a salt thereof, the method including the step of heating hydroquinone and 4-(4-trifluoromethoxyphenoxy)piperidine. This method can produce 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine or a salt thereof in an industrially advantageous manner.
    本发明提供了一种生产1-(4-羟基苯基)-4-(4-三氟甲氧基苯氧基)哌啶或其盐的方法,该方法包括加热对苯二酚和4-(4-三氟甲氧基苯氧基)哌啶的步骤。该方法能以工业上有利的方式生产 1-(4-羟基苯基)-4-(4-三氟甲氧基苯氧基)哌啶或其盐。
  • Method for producing 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine or salt thereof
    申请人:OTSUKA PHARMACEUTICAL CO., LTD.
    公开号:US10252995B2
    公开(公告)日:2019-04-09
    The present invention provides a method for producing 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine or a salt thereof, the method including the step of heating hydroquinone and 4-(4-trifluoromethoxyphenoxy)piperidine. This method can produce 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine or a salt thereof in an industrially advantageous manner.
    本发明提供了一种生产1-(4-羟基苯基)-4-(4-三氟甲氧基苯氧基)哌啶或其盐的方法,该方法包括加热对苯二酚和4-(4-三氟甲氧基苯氧基)哌啶的步骤。该方法能以工业上有利的方式生产 1-(4-羟基苯基)-4-(4-三氟甲氧基苯氧基)哌啶或其盐。
  • US8598358B2
    申请人:——
    公开号:US8598358B2
    公开(公告)日:2013-12-03
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