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5-Phenyl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carbonitrile | 296796-42-4

中文名称
——
中文别名
——
英文名称
5-Phenyl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carbonitrile
英文别名
5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile
5-Phenyl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carbonitrile化学式
CAS
296796-42-4
化学式
C14H7F3N4
mdl
——
分子量
288.23
InChiKey
MJGNWUULORTGBF-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

  • 密度:
    1.41±0.1 g/cm3(Predicted)
  • 溶解度:
    1.6 [ug/mL]

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    54
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • [EN] PYRAZOLO AND IMIDAZO-PYRIMIDINE DERIVATIVES<br/>[FR] DERIVES DE PYRAZOLO-PYRIMIDINE ET D'IMIDAZO-PYRIMIDINE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2005040171A1
    公开(公告)日:2005-05-06
    The present invention relates to novel pyrazolo- and imidazo-pyrimidine derivatives of formula (I) wherein A, D, E, L, M, Q, R1, R2 and R3 are as defined in the description and claims and to processes for their preparation, pharmaceutical compositions containing said derivatives and their use in the prevention and treatment of diseases.
    本发明涉及公式(I)中的新型吡唑啉和咪唑嘧啶生物,其中A、D、E、L、M、Q、R1、R2和R3如描述和索赔中所定义,并涉及其制备方法、含有所述衍生物的药物组合物以及它们在预防和治疗疾病中的用途。
  • Pyrazolo-pyridine
    申请人:Wichmann Juergen
    公开号:US20050130992A1
    公开(公告)日:2005-06-16
    The present invention relates to novel pyrazolo- and imidazo-pyrimidine derivatives of formula I wherein A, D, E, L, M, Q, R 1 , R 2 and R 3 are as defined hereinabove. The present invention also relates to a process for their preparation, a pharmaceutical composition containing said derivatives and a method of treating or preventing acute or chronic neurological disorder comprising administering to a patient in need of such treatment a pharmaceutical composition comprising a therapeutically effective amount of at least one such derivatives. These disorders include acute and chronic disorders
    本发明涉及式I的新型吡唑咪唑嘧啶生物,其中A、D、E、L、M、Q、R1、R2和R3如上所定义。本发明还涉及它们的制备方法,含有该衍生物的药物组合物以及治疗或预防急性或慢性神经障碍的方法,包括向需要该治疗的患者给予含有至少一种该类衍生物的治疗剂量的药物组合物。这些障碍包括急性和慢性障碍。
  • HETEROCYCLIC COMPOUND
    申请人:Mochizuki Michiyo
    公开号:US20110118236A1
    公开(公告)日:2011-05-19
    An object of the present invention is to provide a novel AMPA receptor potentiator. A compound represented by the following formula (I) or a salt thereof: wherein in formula (I) R 1 represents (1) a halogen atom, or (2) cyano group, or the like; Ra and Rb each independently represent a hydrogen atom or C 1-4 alkyl; L represents a bond, or a spacer in which the number of atoms in the main chain is 1 to 8; Ring A represents (1) a non-aromatic carbon ring of 4-8 carbon atoms, or (2) a 4- to 8-membered non-aromatic heterocycle either of which is optionally substituted with 1 or more substituents selected from (a) halogen atoms, and (b) cyano group; and Ar represents a substituted phenyl group, or optionally substituted 5- or 6-membered aromatic heterocyclic group.
    本发明的目的是提供一种新型AMPA受体增强剂。化合物由以下式(I)或其盐所表示:其中在式(I)中,R1表示(1)卤素原子或(2)基等;Ra和Rb各自独立地表示氢原子或C1-4烷基;L表示键或主链中原子数为1至8的间隔物;环A表示(1)4-8个碳原子的非芳香碳环,或(2)4-至8个成员的非芳香杂环,其中任一环均可以选择性地用1个或多个取代基所取代,所述取代基选择自(a)卤素原子和(b)基;Ar表示取代苯基或可选择性取代的5-或6-成员芳香杂环基。
  • PYRAZOLO AND IMIDAZO-PYRIMIDINE DERIVATIVES
    申请人:F. Hoffmann-Roche AG
    公开号:EP1670801A1
    公开(公告)日:2006-06-21
  • US7329662B2
    申请人:——
    公开号:US7329662B2
    公开(公告)日:2008-02-12
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