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methanesulfonic acid cyclopropyl-[5-(2-fluoro-5-methyl-phenyl)-isoxazol-3-yl]-methyl ester | 657425-03-1

中文名称
——
中文别名
——
英文名称
methanesulfonic acid cyclopropyl-[5-(2-fluoro-5-methyl-phenyl)-isoxazol-3-yl]-methyl ester
英文别名
Methanesulfonic acid cyclopropyl-[5-(2-fluoro-5-methyl-phenyl)-isoxazol-3-yl]-methyl ester;[cyclopropyl-[5-(2-fluoro-5-methylphenyl)-1,2-oxazol-3-yl]methyl] methanesulfonate
methanesulfonic acid cyclopropyl-[5-(2-fluoro-5-methyl-phenyl)-isoxazol-3-yl]-methyl ester化学式
CAS
657425-03-1
化学式
C15H16FNO4S
mdl
——
分子量
325.361
InChiKey
KYUQMSSPLNSYTK-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:
    512.7±50.0 °C(Predicted)
  • 密度:
    1.367±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    77.8
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

点击查看最新优质反应信息

文献信息

  • New compounds
    申请人:AstraZeneca AB and NPS Pharmaceuticals, Inc.
    公开号:US20040132726A1
    公开(公告)日:2004-07-08
    The present invention relates to new compounds of formula I, 1 wherein P, Q, X 1 , X 2 , X 3 , X 4 , X 4 , R, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , m, n, o, p and q are defined as in any one of claims 1 to 12, a process for their preparation and new intermediates prepared therein, pharmaceutical formulations containing said compounds and to the use of said compounds in therapy.
    本发明涉及公式I的新化合物,其中P、Q、X1、X2、X3、X4、X4、R、R1、R2、R3、R4、R5、R6、R7、m、n、o、p和q如权利要求书1至12中的任一项所定义,以及其制备过程和制备其中的新中间体,含有该化合物的药物配方和在治疗中使用该化合物的用途。
  • OXADIAZOLES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR-5
    申请人:AstraZeneca AB
    公开号:EP1536790A2
    公开(公告)日:2005-06-08
  • [EN] NEW COMPOUNDS<br/>[FR] NOUVEAUX COMPOSES
    申请人:ASTRAZENECA AB
    公开号:WO2004014370A2
    公开(公告)日:2004-02-19
    The present invention relates to new compounds of formula (I), wherein P, Q, X1, X2, X3, X4, R, R1, R2, R3, R4, R5, R6, R7, m, n, o, p and q are defined as in any one of claims 1 to 12, a process for their preparation and new intermediates prepared therein, pharmaceutical formulations containing said compounds and to the use of said compounds in therapy. It has been found that the compounds according to the present invention, or salts therof, exhibit a high degree of potency and selectivity for individual metabotropic glutamate receptor (mGluR) subtypes. In particular there are compounds according to the present invention that are potent and selective for the mGluR Group I receptor and more particularly for mGluR5. Thus, it is expected that the compounds of the invention are well suited for the prevention and/or treatment of mGluR5 receptor-mediated disorders such as acute and chronic neurological and psychiatric disorders and chronic and acute pain disorders.
  • [EN] OXADIAZOLES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR-5<br/>[FR] NOUVEAUX COMPOSES
    申请人:ASTRAZENECA AB
    公开号:WO2004014370A3
    公开(公告)日:2004-10-21
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