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2-[6-(3-fluorophenylethynyl)-pyridin-3-yl]-5,5-dimethylpyrazolidin-3-one | 1429404-13-6

中文名称
——
中文别名
——
英文名称
2-[6-(3-fluorophenylethynyl)-pyridin-3-yl]-5,5-dimethylpyrazolidin-3-one
英文别名
2-[6-[2-(3-Fluorophenyl)ethynyl]pyridin-3-yl]-5,5-dimethylpyrazolidin-3-one
2-[6-(3-fluorophenylethynyl)-pyridin-3-yl]-5,5-dimethylpyrazolidin-3-one化学式
CAS
1429404-13-6
化学式
C18H16FN3O
mdl
——
分子量
309.343
InChiKey
QMRRRSXADHVFTE-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):
    2.5
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    45.2
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • ETHYNYL DERIVATIVES
    申请人:Hoffmann-La Roche Inc.
    公开号:US20130090332A1
    公开(公告)日:2013-04-11
    The present invention relates to ethynyl derivatives of formula I wherein U, V, Y, R 1 , R 2 , R 2′ , R 3 , R 3′ and R 8 are described herein. It has been found that the compounds of general formula I are allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5).
    本发明涉及公式I的乙炔生物,其中U、V、Y、R1、R2、R2'、R3、R3'和R8如本文所述。已发现通式I的化合物是代谢型谷酸受体亚型5(mGluR5)的变构调节剂。
  • [EN] ETHYNYL DERIVATIVES AS MGLUR5 ALLOSTERIC MODULATORS<br/>[FR] DÉRIVÉS D'ÉTHYNYLE COMME MODULATEURS ALLOSTÉRIQUES DE MGLUR5
    申请人:HOFFMANN LA ROCHE
    公开号:WO2013050454A1
    公开(公告)日:2013-04-11
    The present invention relates to ethynyl derivatives of formula (I) wherein U is N or CH, R8 is hydrogen, halogen, lower alkyl or lower alkoxy;Y is –N(R4)-, -O- or –C(R5R5')-; wherein R4 is hydrogen or lower alkyl and R5/R5' are independently hydrogen, hydroxy, lower alkyl or lower alkoxy; V is –N(R6)- or –C(R7R7'), wherein R6 is hydrogen or lower alkyl and R7/R7' are independently from each other hydrogen, lower alkyl, CH2-lower alkoxy or may form together with the carbon atom to which they are attached a C3-C6-cycloalkyl; R1 is phenyl or heteroaryl, which are optionally substituted by halogen, lower alkyl or lower alkoxy; m is 0 or 1; in case m is 1, R3/R3' are independently from each other hydrogen, lower alkyl, CH2-lower alkoxy or may form together with the carbon atom to which they are attached a C3-C6-cycloalkyl; n is 0 or 1; in case n is 1, R2/R2' are independently from each other hydrogen, lower alkyl, CH2-lower alkoxy or may form together with the carbon atom to which they are attached a C3-C6-cycloalkyl; or if m is 1 and n is 0, R3 and R7 may form together with the carbon atoms to which they are attached a C4-6-cycloalkyl; or if m is 1 and n is 1, R2 and R3 or R3 and R7 may form together with the carbon atoms to which they are attached a C4-6-cycloalkyl; or to a pharmaceutically acceptable acid addition salt, to a racemic mixture, or to its corresponding enantiomer and/or optical isomer and/or stereoisomer thereof. It has been found that the compounds of general formula (I) are allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5).
    本发明涉及公式(I)的乙炔生物,其中U为N或CH,R8为氢、卤素、低烷基或低烷氧基;Y为-N(R4)-、-O-或-C(R5R5')-;其中R4为氢或低烷基,R5/R5'分别独立地为氢、羟基、低烷基或低烷氧基;V为-N(R6)-或-C(R7R7'),其中R6为氢或低烷基,R7/R7'独立地为氢、低烷基、CH2-低烷氧基或可能与其附着的碳原子一起形成C3-C6环烷基;R1为苯或杂环烷基,可以选择性地被卤素、低烷基或低烷氧基取代;m为0或1;如果m为1,则R3/R3'独立地为氢、低烷基、 -低烷氧基或可能与其附着的碳原子一起形成C3-C6环烷基;n为0或1;如果n为1,则R2/R2'独立地为氢、低烷基、 -低烷氧基或可能与其附着的碳原子一起形成C3-C6环烷基;或者如果m为1且n为0,R3和R7可以与其附着的碳原子一起形成C4-6环烷基;或者如果m为1且n为1,R2和R3或R3和R7可以与其附着的碳原子一起形成C4-6环烷基;或者是其对应的药用酸盐、消旋混合物,或其相应的对映体和/或光学异构体和/或立体异构体。已经发现,一般式(I)的化合物是代谢型谷酸受体亚型5(mGluR5)的别构调节剂。
  • ETHYNYL DERIVATIVES AS MGLUR5 ALLOSTERIC MODULATORS
    申请人:F.Hoffmann-La Roche AG
    公开号:EP2763977A1
    公开(公告)日:2014-08-13
  • US8969338B2
    申请人:——
    公开号:US8969338B2
    公开(公告)日:2015-03-03
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