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(RS)-[3-fluoro-5-(3-fluoro-phenylethynyl)-pyridin-2-yl]-(4-hydroxy-2,2-dimethyl-piperidin-1-yl)-methanone | 1403771-10-7

中文名称
——
中文别名
——
英文名称
(RS)-[3-fluoro-5-(3-fluoro-phenylethynyl)-pyridin-2-yl]-(4-hydroxy-2,2-dimethyl-piperidin-1-yl)-methanone
英文别名
[3-Fluoro-5-[2-(3-fluorophenyl)ethynyl]pyridin-2-yl]-(4-hydroxy-2,2-dimethylpiperidin-1-yl)methanone
(RS)-[3-fluoro-5-(3-fluoro-phenylethynyl)-pyridin-2-yl]-(4-hydroxy-2,2-dimethyl-piperidin-1-yl)-methanone化学式
CAS
1403771-10-7
化学式
C21H20F2N2O2
mdl
——
分子量
370.399
InChiKey
WRUPHINGSCUMEA-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):
    3.4
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    53.4
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • PHENYL OR PYRIDINYL-ETHYNYL DERIVATIVES
    申请人:Jaeschke Georg
    公开号:US20120270852A1
    公开(公告)日:2012-10-25
    The present invention relates to ethynyl derivatives of formula I wherein Y is N or C—R 3 ; R 3 is hydrogen, methyl, halogen or nitrile; R 1 is phenyl or pyridinyl, each of which is optionally substituted by halogen, lower alkyl or lower alkoxy; R 2 /R 2′ are each independently hydrogen, lower alkyl or lower alkyl substituted by halogen, or R 2 and R 2′ together with the N-atom to which they are attached form a morpholine ring, a piperidine ring or an azetidine ring, each of which is unsubstituted or substituted one or more substituents selected from lower alkoxy, halogen, hydroxy and methyl; R 4 /R 4′ are each independently hydrogen or lower alkyl, or R 4 and R 4′ together form a C 3-5 cycloalkyl-, tetrahydrofuran- or an oxetane-ring; 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. Compounds of formula I are positive allosteric modulators (PAM) of the metabotropic glutamate receptor subtype 5 (mGluR5).
    本发明涉及公式I的乙炔生物,其中Y为N或C—R3;R3为氢、甲基、卤素或腈基;R1为苯基或吡啶基,每个基团可选择地被卤素、低烷基或低烷氧基取代;R2/R2′各自独立地为氢、低烷基或被卤素取代的低烷基,或者R2和R2′与它们连接的N原子一起形成一个吗啉环、哌啶环或氮杂环,每个环未取代或取代一个或多个从低烷氧基、卤素、羟基和甲基中选取的取代基;R4/R4′各自独立地为氢或低烷基,或者R4和R4′一起形成一个C3-5环烷基、四氢呋喃环或噁唑环;或者形成药用可接受的酸盐、对映体混合物,或其对应的对映体和/或光学异构体和/或立体异构体。公式I的化合物是代谢型谷酸受体亚型5(mGluR5)的正向变构调节子(PAM)。
  • [EN] 5-(PHENYL/PYRIDINYL-ETHINYL)-2-PYRIDINE/ 2-PYRIMIDINE-CARBORXAMIDES AS MGLUR5 MODULATORS<br/>[FR] 5-(PHÉNYL/PYRIDINYL-ÉTHINYL)-2-PYRIDINE/2 PYRIMIDINE-CARBOXAMIDES COMME MODULATEUR DE MGLUR5
    申请人:HOFFMANN LA ROCHE
    公开号:WO2012143340A1
    公开(公告)日:2012-10-26
    The present invention relates to ethynyl derivatives of formula (I), wherein, Y is N or C-R3;and R3 is hydrogen, methyl, halogen or nitrile; R1 is phenyl or pyridinyl, which are optionally substituted by halogen, lower alkyl or lower alkoxy; R2/R2' are independently from each other hydrogen, lower alkyl or lower alkyl substituted by halogen, or R2 and R2' may form together with the N-atom to which they are attached a morpholine ring, a piperidine ring or an azetidine ring, which are unsubstituted or substituted one or more substituents selected from lower alkoxy, halogen, hydroxy or methyl; R4/R4' are independently from each other hydrogen or lower alkyl, or R4 and R4' form together a C3-5 cycloalkyl-, tetrahydrofuran- or an oxetane-ring; 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 now surprisingly been found that the compounds of general formula (I) are positive allosteric modulators (PAM) of the metabotropic glutamate receptor subtype 5 (mGluR5).
    本发明涉及公式(I)的乙炔生物,其中,Y是N或C-R3;R3是氢、甲基、卤素或腈基;R1是苯基或吡啶基,可以选择地被卤素、低烷基或低烷氧基取代;R2/R2'分别是氢、低烷基或被卤素取代的低烷基,或者R2和R2'可以与它们连接的N原子一起形成吗啡啉环、哌啶环或氮杂环,该环未被取代或被一个或多个从低烷氧基、卤素、羟基或甲基中选择的取代基取代;R4/R4'分别是氢或低烷基,或者R4和R4'一起形成C3-5环烷基、四氢呋喃环或氧杂环;或者是药学上可接受的酸盐,或者是消旋混合物,或者是其对应的对映体和/或光学异构体和/或立体异构体。令人惊讶的是发现,通用公式(I)的化合物是代谢型谷酸受体亚型5(mGluR5)的阳性变构调节剂(PAM)。
  • 5-(PHENYL/PYRIDINYL-ETHINYL)-2-PYRIDINE/ 2-PYRIMIDINE-CARBORXAMIDES AS MGLUR5 MODULATORS
    申请人:F. Hoffmann-La Roche AG
    公开号:EP2699547A1
    公开(公告)日:2014-02-26
  • 5-(PHENYL/PYRIDINYL-ETHINYL)-2-PYRIDINE/2-PYRIMIDINE-CARBORXAMIDES AS MGLUR5 MODULATORS
    申请人:F. Hoffmann-La Roche AG
    公开号:EP2699547B1
    公开(公告)日:2015-03-04
  • US8772300B2
    申请人:——
    公开号:US8772300B2
    公开(公告)日:2014-07-08
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