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3-(4-methoxy-phenylthio)-4,5,6-trimethyl-1-phenyl-1H-pyridine-2-one | 918543-42-7

中文名称
——
中文别名
——
英文名称
3-(4-methoxy-phenylthio)-4,5,6-trimethyl-1-phenyl-1H-pyridine-2-one
英文别名
3-[(4-Methoxyphenyl)sulfanyl]-4,5,6-trimethyl-1-phenylpyridin-2(1H)-one;3-(4-methoxyphenyl)sulfanyl-4,5,6-trimethyl-1-phenylpyridin-2-one
3-(4-methoxy-phenylthio)-4,5,6-trimethyl-1-phenyl-1H-pyridine-2-one化学式
CAS
918543-42-7
化学式
C21H21NO2S
mdl
——
分子量
351.469
InChiKey
IODHUWFYLWQHBY-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):
    4.4
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    54.8
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    N-(1,2-dimethyl-3-oxo-1-butenyl)-2-(4-methoxy-phenylthio)-N-phenyl-acetamide 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 四氢呋喃 为溶剂, 反应 14.17h, 以47.8%的产率得到3-(4-methoxy-phenylthio)-4,5,6-trimethyl-1-phenyl-1H-pyridine-2-one
    参考文献:
    名称:
    WO2007/4543
    摘要:
    公开号:
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文献信息

  • PHARMACEUTICAL COMPOSITIONS CONTAINING 2-PYRIDONE DERIVATIVES AS EFFECTIVE COMPONENTS
    申请人:Kato Masatoshi
    公开号:US20090298889A1
    公开(公告)日:2009-12-03
    The present invention herein provides a 2-pyridone derivative which has a cell adhesion-inhibitory activity and which is useful for preventing and/or treating pathema or disease conditions including, for instance, inflammations which relate to leukocytic infiltration. The 2-pyridone derivative is a compound represented by the following general formula (1). In the formula, R 1 represents, for instance, a phenyl or pyridyl group, R 2 represents, for instance, a phenyl group, R 3 represents, for instance, a lower alkyl group, R 4 represents, for instance, a lower alkyl group, R 5 represents, for instance, a lower alkyl group, and R 6 represents, for instance, a lower alkyl group.
    本发明提供了一种2-吡啶酮衍生物,该衍生物具有细胞黏附抑制活性,并可用于预防和/或治疗包括与白细胞浸润有关的炎症在内的病理或疾病状况。2-吡啶酮衍生物是由以下通式(1)表示的化合物。在该式中,R1代表例如苯基或吡啶基,R2代表例如苯基,R3代表例如较低的烷基,R4代表例如较低的烷基,R5代表例如较低的烷基,R6代表例如较低的烷基。
  • PHARMACEUTICAL COMPOSITION COMPRISING 2-PYRIDONE DERIVATIVE AS ACTIVE INGREDIENT
    申请人:Sato Pharmaceutical Co. Ltd.
    公开号:EP1897870A1
    公开(公告)日:2008-03-12
    The present invention herein provides a 2-pyridone derivative which has a cell adhesion-inhibitory activity and which is useful for preventing and/or treating pathema or disease conditions including, for instance, inflammations which relate to leukocytic infiltration. The 2-pyridone derivative is a compound represented by the following general formula (1). In the formula, R1 represents, for instance, a phenyl or pyridyl group, R2 represents, for instance, a phenyl group, R3 represents, for instance, a lower alkyl group, R4 represents, for instance, a lower alkyl group, R5 represents, for instance, a lower alkyl group, and R6 represents, for instance, a lower alkyl group:
    本发明提供了一种 2-吡啶酮衍生物,它具有细胞粘附抑制活性,可用于预防和/或治疗病变或疾病,包括例如与白细胞浸润有关的炎症。2 吡啶酮衍生物是由以下通式(1)表示的化合物。式中,R1 代表苯基或吡啶基,R2 代表苯基,R3 代表低级烷基,R4 代表低级烷基,R5 代表低级烷基,R6 代表低级烷基:
  • WO2007/4543
    申请人:——
    公开号:——
    公开(公告)日:——
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