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3-methyl-6-(piperazin-1-yl)-2-((2-(trifluoromethyl)phenoxy)methyl)pyrimidin-4(3H)-one | 1191919-28-4

中文名称
——
中文别名
——
英文名称
3-methyl-6-(piperazin-1-yl)-2-((2-(trifluoromethyl)phenoxy)methyl)pyrimidin-4(3H)-one
英文别名
3-methyl-6-piperazin-1-yl-2-[[2-(trifluoromethyl)phenoxy]methyl]pyrimidin-4-one
3-methyl-6-(piperazin-1-yl)-2-((2-(trifluoromethyl)phenoxy)methyl)pyrimidin-4(3H)-one化学式
CAS
1191919-28-4
化学式
C17H19F3N4O2
mdl
——
分子量
368.359
InChiKey
NONLLKWVHQMTNE-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):
    1.7
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    57.2
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    哌嗪 、 6-chloro-3-methyl-2-((2-(trifluoromethyl)phenoxy)methyl)pyrimidin-4(3H)-one 以 乙醇 为溶剂, 生成 3-methyl-6-(piperazin-1-yl)-2-((2-(trifluoromethyl)phenoxy)methyl)pyrimidin-4(3H)-one
    参考文献:
    名称:
    Design and synthesis of piperazinylpyrimidinones as novel selective 5-HT2C agonists
    摘要:
    This Letter reports the design and synthesis of several novel series of piperazinyl pyrimidinones as 5-HT2C agonists. Several of the compounds presented exhibit good in vitro potency and selectivity over the closely related 5-HT2A and 5-HT2B receptors. Compound 11 was active in in vivo models of stress urinary incontinence. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.07.133
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文献信息

  • Design and synthesis of piperazinylpyrimidinones as novel selective 5-HT2C agonists
    作者:Mark D. Andrews、Martin P. Green、Charlotte M.N. Allerton、David V. Batchelor、Julian Blagg、Alan D. Brown、David W. Gordon、Gordon McMurray、Daniel J. Millns、Carly L. Nichols、Lesa Watson
    DOI:10.1016/j.bmcl.2009.07.133
    日期:2009.9
    This Letter reports the design and synthesis of several novel series of piperazinyl pyrimidinones as 5-HT2C agonists. Several of the compounds presented exhibit good in vitro potency and selectivity over the closely related 5-HT2A and 5-HT2B receptors. Compound 11 was active in in vivo models of stress urinary incontinence. (C) 2009 Elsevier Ltd. All rights reserved.
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