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2-(chloromethyl)-5,6,7,8-tetrahydroquinazolin-4(3H)-one | 145475-35-0

中文名称
——
中文别名
——
英文名称
2-(chloromethyl)-5,6,7,8-tetrahydroquinazolin-4(3H)-one
英文别名
2-(chloromethyl)-5,6,7,8-tetrahydro-4(3H)-quinazolinone;2-(Chloromethyl)-5,6,7,8-tetrahydroquinazolin-4(3H)-one;2-(chloromethyl)-5,6,7,8-tetrahydro-3H-quinazolin-4-one
2-(chloromethyl)-5,6,7,8-tetrahydroquinazolin-4(3H)-one化学式
CAS
145475-35-0
化学式
C9H11ClN2O
mdl
——
分子量
198.652
InChiKey
YOEVSDYLLYABRV-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):
    1.1
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    41.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    氯乙酰胺盐酸盐2-环己酮甲酸乙酯三乙胺 作用下, 以 甲醇 为溶剂, 反应 60.0h, 以13%的产率得到2-(chloromethyl)-5,6,7,8-tetrahydroquinazolin-4(3H)-one
    参考文献:
    名称:
    [EN] NOVEL 2-PIPERIDIN-1-YL-ACETAMIDE COMPOUNDS FOR USE AS TANKYRASE INHIBITORS
    [FR] NOUVEAUX COMPOSÉS 2-PIPERIDIN-1-YL-ACETAMIDE UTILISABLES EN TANT QU'INHIBITEURS DE TANKYRASE
    摘要:
    本发明提供了式(I)的化合物,其中R1-R5和L在此处定义。本发明还提供了包含式(I)化合物的药物组合物和组合物,以及将这些化合物用作坦基酶抑制剂以及用于治疗Wnt信号和坦基酶1和2信号相关疾病的用途,包括但不限于癌症。
    公开号:
    WO2013012723A1
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文献信息

  • [EN] BENZOXAZINONE DERIVATIVES FOR THE TREATMENT OF GLYTL MEDIATED DISORDERS<br/>[FR] DÉRIVÉS DE BENZOXAZINONE POUR TRAITER DES TROUBLES INDUITS PAR GLYTL
    申请人:GLAXO GROUP LTD
    公开号:WO2011012622A1
    公开(公告)日:2011-02-03
    The present invention relates to benzoxazinone derivatives, processes for their preparation, pharmaceutical compositions and medicaments containing them and to their use in treating disorders mediated by GlyT1, including neurological and neuropsychiatric disorders, in particular psychoses, dementia or attention deficit disorder.
    本发明涉及苯并噁唑酮衍生物,其制备方法,含有它们的药物组合物和药物,以及它们在治疗由GlyT1介导的疾病中的应用,包括神经系统和神经精神疾病,特别是精神病、痴呆或注意力缺陷障碍。
  • NOVEL 2-PIPERIDIN-1-YL-ACETAMIDE COMPOUNDS FOR USE AS TANKYRASE INHIBITORS
    申请人:Cheung Atwood Kim
    公开号:US20150025070A1
    公开(公告)日:2015-01-22
    The present invention provides for compounds of formula (I): wherein R 1 -R 5 and L are defined herein. The present invention also provides for pharmaceutical compositions and combinations comprising a compound of formula (I) as well as for the use of such compounds as tankyrase inhibitors and in the treatment of Wnt signaling and tankyrase 1 and 2 signaling related disorders which include, but are not limited to, cancer.
    本发明提供了公式(I)的化合物:其中R1-R5和L在此定义。本发明还提供了含有公式(I)化合物的药物组合物和组合物,以及将这些化合物用作坦克酶抑制剂和治疗与Wnt信号和坦克酶1和2信号相关的疾病的用途,包括但不限于癌症。
  • 2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors
    申请人:Cheung Atwood Kim
    公开号:US09181266B2
    公开(公告)日:2015-11-10
    The present invention provides for compounds of formula (I): wherein R1-R5 and L are defined herein. The present invention also provides for pharmaceutical compositions and combinations comprising a compound of formula (I) as well as for the use of such compounds as tankyrase inhibitors and in the treatment of Wnt signaling and tankyrase 1 and 2 signaling related disorders which include, but are not limited to, cancer.
    本发明提供了式(I)的化合物,其中R1-R5和L如本文所定义。本发明还提供了包含式(I)化合物的药物组合物和制剂,以及将这些化合物用作坦克酶抑制剂和治疗Wnt信号和与坦克酶1和2信号相关的疾病的用途,包括但不限于癌症。
  • A novel ring transformation of oxazinones and azetidinones into pyrimidinones
    作者:Shinichi Kawamura、Yuzuru Sanemitsu
    DOI:10.1021/jo00054a026
    日期:1993.1
    Azetidinones or oxazinones, being easily prepared from enamines and acyl isocyanates, were transformed into highly substituted 4(3H)-pyrimidinones upon treatment with ammonium acetate. This novel ring transformation was also accomplished through a one-pot reaction without isolation of the adduct.
  • US9181266B2
    申请人:——
    公开号:US9181266B2
    公开(公告)日:2015-11-10
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