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3-[3-(dimethylamino)prop-2-enoyl]-1-pyridin-4-ylpyridazin-4(1H)-one | 1240649-13-1

中文名称
——
中文别名
——
英文名称
3-[3-(dimethylamino)prop-2-enoyl]-1-pyridin-4-ylpyridazin-4(1H)-one
英文别名
3-((E)-3-dimethylamino-acryloyl)-1-pyridin-4-yl-1H-pyridazin-4-one;3-[(E)-3-(dimethylamino)prop-2-enoyl]-1-pyridin-4-ylpyridazin-4-one
3-[3-(dimethylamino)prop-2-enoyl]-1-pyridin-4-ylpyridazin-4(1H)-one化学式
CAS
1240649-13-1
化学式
C14H14N4O2
mdl
——
分子量
270.291
InChiKey
WWULWJUFBDFUPV-WEVVVXLNSA-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):
    0.7
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    65.9
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    3-[3-(dimethylamino)prop-2-enoyl]-1-pyridin-4-ylpyridazin-4(1H)-one2-氯-6-肼基吡啶溶剂黄146 作用下, 以 乙醇 为溶剂, 反应 0.75h, 以12%的产率得到3-[2-(6-chloropyridin-2-yl)-2H-pyrazol-3-yl]-1-pyridin-4-yl-1H-pyridazin-4-one
    参考文献:
    名称:
    HETEROARYL SUBSTITUTED PYRIDAZINONE DERIVATIVES
    摘要:
    本发明涉及具有如下式(I)的新型吡啶并嗪酮衍生物,其中R1、R2、R3和R4如描述和索赔中所定义,并且其生理上可接受的盐和酯。这些化合物抑制PDE10A并可用作药物。
    公开号:
    US20100216793A1
  • 作为产物:
    描述:
    3-(pyridin-4-ylazo)pentane-2,4-dioneN,N-二甲基甲酰胺二甲基缩醛 反应 1.0h, 以55%的产率得到3-[3-(dimethylamino)prop-2-enoyl]-1-pyridin-4-ylpyridazin-4(1H)-one
    参考文献:
    名称:
    HETEROARYL SUBSTITUTED PYRIDAZINONE DERIVATIVES
    摘要:
    本发明涉及具有如下式(I)的新型吡啶并嗪酮衍生物,其中R1、R2、R3和R4如描述和索赔中所定义,并且其生理上可接受的盐和酯。这些化合物抑制PDE10A并可用作药物。
    公开号:
    US20100216793A1
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文献信息

  • Pyridazinone compounds
    申请人:Taniguchi Takahiko
    公开号:US20100197651A1
    公开(公告)日:2010-08-05
    The present invention provides a compound which has the effect of PDE inhibition, and which is useful as a medicament for preventing or treating schizophrenia or so on. A compound of formula (I 0 ): wherein R 1 represents a substituent, R 2 represents a hydrogen atom, or a substituent, R 3 represents a hydrogen atom, or a substituent, Ring A represents an aromatic ring which can be substituted, and Ring B represents a 5-membered heteroaromatic ring which can be substituted, or a salt thereof.
    本发明提供了一种具有PDE抑制作用并且用作预防或治疗精神分裂症等病症的药物的化合物。该化合物的公式为(I0):其中,R1代表一个取代基,R2代表一个氢原子或一个取代基,R3代表一个氢原子或一个取代基,环A代表一个可被取代的芳香环,而环B代表一个可被取代的5元杂芳环,或其盐。
  • PYRIDAZINONE COMPOUNDS
    申请人:TANIGUCHI Takahiko
    公开号:US20120277204A1
    公开(公告)日:2012-11-01
    The present invention provides a compound which has the effect of PDE inhibition, and which is useful as a medicament for preventing or treating schizophrenia or so on. A compound of formula (I 0 ), wherein R1 represents a substituent; R2 represents a hydrogen atom, or a substituent; R3 represents a hydrogen atom, or a substituent; Ring A represents an aromatic ring which can be substituted, and Ring B represents a 5-membered heteroaromatic ring which can be substituted, or a salt thereof.
    本发明提供了一种具有PDE抑制作用的化合物,可用作预防或治疗精神分裂症等药物。化合物的式子为(I0),其中R1代表取代基;R2代表氢原子或取代基;R3代表氢原子或取代基;环A代表可取代的芳香环,环B代表可取代的五元杂环芳基环或其盐。
  • PYRIDAZINONE COMPOUNDS AS PHOSPHODIESTERASE INHIBITORS AND METHODS OF TREATING DISORDERS
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US20150099757A1
    公开(公告)日:2015-04-09
    The present invention provides a compound which has the effect of PDE inhibition, and which is useful as a medicament for preventing or treating schizophrenia or so on. A compound of formula (I 0 ): wherein R 1 represents a substituent, R 2 represents a hydrogen atom, or a substituent, R 3 represents a hydrogen atom, or a substituent, Ring A represents an aromatic ring which can be substituted, and Ring B represents a 5-membered heteroaromatic ring which can be substituted, or a salt thereof.
    本发明提供了一种具有PDE抑制作用的化合物,可用作预防或治疗精神分裂症等药物。该化合物的化学式为(I0),其中R1代表取代基,R2代表氢原子或取代基,R3代表氢原子或取代基,环A代表可被取代的芳香环,环B代表可被取代的五元杂环芳香环,或其盐。
  • Substituted pyridazines as PDE10A inhibitors
    申请人:Alberati Daniela
    公开号:US09187455B2
    公开(公告)日:2015-11-17
    The present invention is concerned with novel pyridazinone derivatives of formula (I) wherein R1, R2, R3 and R4 are as defined in the description and in the claims, as well as physiologically acceptable salts and esters thereof. These compounds inhibit PDE10A and can be used as pharmaceuticals.
    本发明涉及式(I)的新型吡啶并咪唑酮衍生物,其中R1、R2、R3和R4如描述和权利要求中所定义,以及其生理上可接受的盐和酯。这些化合物抑制PDE10A并可用作药物。
  • US8354411B2
    申请人:——
    公开号:US8354411B2
    公开(公告)日:2013-01-15
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