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(6-bromopyrazolo[1,5-a]pyrimidin-2-yl)(3,4-dihydroisoquinolin-2(1H)-yl)methanone

中文名称
——
中文别名
——
英文名称
(6-bromopyrazolo[1,5-a]pyrimidin-2-yl)(3,4-dihydroisoquinolin-2(1H)-yl)methanone
英文别名
(6-bromopyrazolo[1,5-a]pyrimidin-2-yl)-(3,4-dihydro-1H-isoquinolin-2-yl)methanone
(6-bromopyrazolo[1,5-a]pyrimidin-2-yl)(3,4-dihydroisoquinolin-2(1H)-yl)methanone化学式
CAS
——
化学式
C16H13BrN4O
mdl
——
分子量
357.2
InChiKey
PPFVMPKRZPPZFQ-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):
    2.3
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    50.5
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • Pyrazolopyrimidines, a process for their preparation and their use as medicine
    申请人:Danysz Wojciech
    公开号:US20080032998A1
    公开(公告)日:2008-02-07
    Substituted pyrazolopyrimidine derivatives of formula (I) wherein R 1 represents chloro or bromo; R 2 , R 3 , R 4 , R 5 , R 6 and R 7 independently represent e.g. hydrogen or C 1-6 -alkyl; R 8 represents a radical R 9 or a radical R 10 , whereby one of the two radicals R 8 represents R 9 and the other radical R 8 represents Ret; R 9 represents e.g. a phenyl or thiophene group, and R 10 represents e.g. hydrogen or methyl; are potent mGluR5 modulators and are useful for the prevention of acute and chronic neurological disorders.
    取代吡唑嘧啶生物的公式(I) 其中 R1代表; R2、R3、R4、R5、R6和R7独立代表例如氢或C1-6-烷基; R8代表R9的基团或R10的基团,其中两个R8基团之一代表R9,另一个R8基团代表Ret;R9代表例如苯基或噻吩基团,R10代表例如氢或甲基; 是有效的mGluR5调节剂,可用于预防急性和慢性神经障碍。
  • Substituted pyrazolopyrimidines, a process for their preparation and their use as medicine
    申请人:Danysz Wojciech
    公开号:US20080039458A1
    公开(公告)日:2008-02-14
    Substituted pyrazolopyrimidine derivatives of formula (I) wherein Y 1 , Y 2 , Y 3 , Y 4 represent N or C—, whereby at least two of the groups Y 1 to Y 4 represent a carbon atom, R 1 represents chloro or bromo, R 2 to R 7 represent e.g. hydrogen, methyl or ethyl; and R 10 and R 11 independently represent e.g. hydrogen or C 1 -C 6 alkyl, are potent mGluR5 modulators and are useful for the prevention of acute and chronic neurological disorders.
    式(I)中的取代嘧唑嘧啶生物,其中Y1、Y2、Y3、Y4代表N或C—,其中至少两个Y1到Y4代表碳原子,R1代表,R2到R7代表氢、甲基或乙基等,而R10和R11独立地代表氢或C1-C6烷基。这些衍生物是有效的mGluR5调节剂,并可用于预防急性和慢性神经系统疾病。
  • Pyrazolopyrimidines for treating CNS disorders
    申请人:Danysz Wojciech
    公开号:US20110212956A1
    公开(公告)日:2011-09-01
    Substituted pyrazolopyrimidine derivatives of formula (I) wherein Y 1 , Y 2 , Y 3 , Y 4 represent N or C—, whereby at least two of the groups Y 1 to Y 4 represent a carbon atom, R 1 represents chloro or bromo, R 2 to R7 represent e.g. hydrogen, methyl or ethyl; and R 10 and R 11 independently represent e.g. hydrogen or C 1 -C 6 alkyl, are potent mGluR5 modulators and are useful for the prevention of acute and chronic neurological disorders.
    公式(I)的替代嘧唑嘧啶生物,其中Y1,Y2,Y3,Y4代表N或C-,其中至少有两个Y1至Y4代表碳原子,R1代表,R2至R7代表氢,甲基或乙基等基团; 而R10和R11分别代表氢或C1-C6烷基,是有效的mGluR5调节剂,并可用于预防急性和慢性神经系统疾病。
  • PYRAZOLOPYRIMIDINES, A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICINE
    申请人:Henrich Markus
    公开号:US20110003820A1
    公开(公告)日:2011-01-06
    The invention relates to pyrazolopyrimidine derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are mGluR5 modulators and are therefore useful for the control and prevention of acute and/or chronic neurological disorders.
    本发明涉及吡唑嘧啶生物及其药学上可接受的盐。本发明还涉及制备这些化合物的方法。本发明的化合物是mGluR5调节剂,因此对于控制和预防急性和/或慢性神经系统疾病有用。
  • SUBSTITUTED PYRAZOLOPYRIMIDINES, A PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICINE
    申请人:Merz Pharma GmbH & Co. KGaA
    公开号:EP2054416A1
    公开(公告)日:2009-05-06
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