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N-[2-(methylthio)-4-oxoquinazolin-3(4H)-yl]methanesulfonamide | 1018471-60-7

中文名称
——
中文别名
——
英文名称
N-[2-(methylthio)-4-oxoquinazolin-3(4H)-yl]methanesulfonamide
英文别名
N-(2-methylsulfanyl-4-oxoquinazolin-3-yl)methanesulfonamide
N-[2-(methylthio)-4-oxoquinazolin-3(4H)-yl]methanesulfonamide化学式
CAS
1018471-60-7
化学式
C10H11N3O3S2
mdl
——
分子量
285.348
InChiKey
JWCSYWGZNUXYJF-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:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    113
  • 氢给体数:
    1
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    N-(methylsulfonyl)-N-[2-(methylthio)-4-oxoquinazolin-3(4H)-yl]methanesulfonamide氢氧化钾 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以86%的产率得到N-[2-(methylthio)-4-oxoquinazolin-3(4H)-yl]methanesulfonamide
    参考文献:
    名称:
    Copper‐Catalyzed Coupling Reaction of 2‐Thioxo‐4‐quinazolinone and Thieno[3,2‐d]pyrimidin‐4‐one Methane Sulphonamide with Aryl Iodides: Preparation of Potential COX‐2 Selective Inhibitors
    摘要:
    Thio-aryl methane sulfonamide derivatives of 4-quinazolinone and thieno[2,3-d]pyrimidin-4-one were synthesized using powdery copper/copper(I) iodide as catalyst; their structural elucidation is also reported. These derivatives were planned as sulfur bioisosteres of selective COX-2 inhibitor drugs.
    DOI:
    10.1080/00397910701820236
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文献信息

  • Copper‐Catalyzed Coupling Reaction of 2‐Thioxo‐4‐quinazolinone and Thieno[3,2‐<i>d</i>]pyrimidin‐4‐one Methane Sulphonamide with Aryl Iodides: Preparation of Potential COX‐2 Selective Inhibitors
    作者:Antonio Perdicaro、Giuseppe Granata、Agostino Marrazzo、Andrea Santagati
    DOI:10.1080/00397910701820236
    日期:2008.2.13
    Thio-aryl methane sulfonamide derivatives of 4-quinazolinone and thieno[2,3-d]pyrimidin-4-one were synthesized using powdery copper/copper(I) iodide as catalyst; their structural elucidation is also reported. These derivatives were planned as sulfur bioisosteres of selective COX-2 inhibitor drugs.
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