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2-carbamoylmethylthio-4-chloro-N-(3,4-dihydro-4-oxoquinazolin-2-yl)-5-methylbenzenesulfonamide | 1421611-04-2

中文名称
——
中文别名
——
英文名称
2-carbamoylmethylthio-4-chloro-N-(3,4-dihydro-4-oxoquinazolin-2-yl)-5-methylbenzenesulfonamide
英文别名
——
2-carbamoylmethylthio-4-chloro-N-(3,4-dihydro-4-oxoquinazolin-2-yl)-5-methylbenzenesulfonamide化学式
CAS
1421611-04-2
化学式
C17H15ClN4O4S2
mdl
——
分子量
438.915
InChiKey
UFHSFJLDRMNYLQ-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

反应信息

  • 作为产物:
    描述:
    邻氨基苯甲酸甲酯溶剂黄146 为溶剂, 以41%的产率得到2-carbamoylmethylthio-4-chloro-N-(3,4-dihydro-4-oxoquinazolin-2-yl)-5-methylbenzenesulfonamide
    参考文献:
    名称:
    Synthesis and antibacterial activity of novel 4-chloro-2-mercaptobenzenesulfonamide derivatives
    摘要:
    Few series of novel 4-chloro-2-mercaptobenzenesulfonamides have been synthesized by the reactions of N-(benzenesulfonyl) cyanamide potassium salts 7-15 with corresponding hydrazinecarbodithioic acid esters, 1-substituted carbothioic acid hydrazides, methyl 3-aminothiophene-2-carboxylate, methyl 2-aminobenzoate, 2-aminophenol or 2-aminothiophenol. The synthesized compounds (16-49) were screened in vitro for their antibacterial activity. Some of the tested compounds 16, 17, 23, 24, 31, 32 and 48 showed the promising activity against many of anaerobic Gram-positive bacteria strains.
    DOI:
    10.3109/14756366.2011.625024
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