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4-Ethyl-1,1-dioxo-2,3-dihydro-1lambda6,2,4-benzothiadiazine-7-carboxylic acid | 945388-14-7

中文名称
——
中文别名
——
英文名称
4-Ethyl-1,1-dioxo-2,3-dihydro-1lambda6,2,4-benzothiadiazine-7-carboxylic acid
英文别名
4-ethyl-1,1-dioxo-2,3-dihydro-1λ6,2,4-benzothiadiazine-7-carboxylic acid
4-Ethyl-1,1-dioxo-2,3-dihydro-1lambda6,2,4-benzothiadiazine-7-carboxylic acid化学式
CAS
945388-14-7
化学式
C10H12N2O4S
mdl
——
分子量
256.282
InChiKey
UVQMKMWZHPPHKY-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):
    0.8
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    95.1
  • 氢给体数:
    2
  • 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

  • 作为反应物:
    描述:
    4-Ethyl-1,1-dioxo-2,3-dihydro-1lambda6,2,4-benzothiadiazine-7-carboxylic acid苯酚N,N'-羰基二咪唑1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 以32%的产率得到Phenyl 4-ethyl-1,1-dioxo-2,3-dihydro-1lambda6,2,4-benzothiadiazine-7-carboxylate
    参考文献:
    名称:
    Design, Synthesis, and Pharmacology of Novel 7-Substituted 3,4-Dihydro-2H-1,2,4-benzothiadiazine 1,1-Dioxides as Positive Allosteric Modulators of AMPA Receptors
    摘要:
    A series of 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxides have been synthesized and evaluated as potentiators of AMPA receptors. Attention was paid to the impact of the substituent introduced at the 7-position of the heterocycle. The biological evaluation was achieved by measuring the AMPA current in rat cortex mRNA-injected Xenopus oocytes. The most potent compound, 4-ethyl-7-fluoro-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide (12a) was found to be active in an object recognition test in rats demonstrating cognition enhancing effects in vivo after oral administration.
    DOI:
    10.1021/jm070120i
  • 作为产物:
    描述:
    methyl 4H-1,2,4-benzothiadiazine-7-carboxylate 1,1-dioxide 在 sodium hydroxide 、 sodium tetrahydroborate 、 potassium carbonate 作用下, 以 甲醇异丙醇乙腈 为溶剂, 反应 4.25h, 生成 4-Ethyl-1,1-dioxo-2,3-dihydro-1lambda6,2,4-benzothiadiazine-7-carboxylic acid
    参考文献:
    名称:
    Design, Synthesis, and Pharmacology of Novel 7-Substituted 3,4-Dihydro-2H-1,2,4-benzothiadiazine 1,1-Dioxides as Positive Allosteric Modulators of AMPA Receptors
    摘要:
    A series of 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxides have been synthesized and evaluated as potentiators of AMPA receptors. Attention was paid to the impact of the substituent introduced at the 7-position of the heterocycle. The biological evaluation was achieved by measuring the AMPA current in rat cortex mRNA-injected Xenopus oocytes. The most potent compound, 4-ethyl-7-fluoro-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide (12a) was found to be active in an object recognition test in rats demonstrating cognition enhancing effects in vivo after oral administration.
    DOI:
    10.1021/jm070120i
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文献信息

  • Design, Synthesis, and Pharmacology of Novel 7-Substituted 3,4-Dihydro-2<i>H</i>-1,2,4-benzothiadiazine 1,1-Dioxides as Positive Allosteric Modulators of AMPA Receptors
    作者:Pierre Francotte、Pascal de Tullio、Eric Goffin、Gaëlle Dintilhac、Emmanuel Graindorge、Pierre Fraikin、Pierre Lestage、Laurence Danober、Jean-Yves Thomas、Daniel-Henri Caignard、Bernard Pirotte
    DOI:10.1021/jm070120i
    日期:2007.6.1
    A series of 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxides have been synthesized and evaluated as potentiators of AMPA receptors. Attention was paid to the impact of the substituent introduced at the 7-position of the heterocycle. The biological evaluation was achieved by measuring the AMPA current in rat cortex mRNA-injected Xenopus oocytes. The most potent compound, 4-ethyl-7-fluoro-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide (12a) was found to be active in an object recognition test in rats demonstrating cognition enhancing effects in vivo after oral administration.
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