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3-(2-methoxyphenyl)-4-(methylthio)-1H-pyrrole-2,5-dione | 398130-18-2

中文名称
——
中文别名
——
英文名称
3-(2-methoxyphenyl)-4-(methylthio)-1H-pyrrole-2,5-dione
英文别名
3-(2-Methoxyphenyl)-4-methylsulfanylpyrrole-2,5-dione
3-(2-methoxyphenyl)-4-(methylthio)-1H-pyrrole-2,5-dione化学式
CAS
398130-18-2
化学式
C12H11NO3S
mdl
——
分子量
249.29
InChiKey
DCASEWUDIBTIHU-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

物化性质

  • 沸点:
    440.9±45.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    80.7
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    3-(2-methoxyphenyl)-4-(methylthio)-1H-pyrrole-2,5-dione碘甲烷potassium carbonate 作用下, 以 丙酮 为溶剂, 以94%的产率得到3-(2-Methoxyphenyl)-1-methyl-4-methylsulfanylpyrrole-2,5-dione
    参考文献:
    名称:
    Synthesis of 3-Methylthio-4-aryl-3-pyrroline-2,5-diones and 3-Arylpyrrolidine-2,5-diones by Reaction of Nitroketene Dithioacetal with Arylacetonitriles
    摘要:
    The reaction of nitroketene dithioacetal (1a), i.e., 2,2-bis(methylthio)-1-nitroethylene, with arylacetonitriles (2a-I) in the presence of the base like sodium hydroxide gave 4-nitrobut-2-enenitriles (3a-I) which were converted into 5-hydroxyimino-4-methylthio-3-phenyl-3-pyrrolin-2-ones (4a-i) under refluxing in methanol. Title compounds (5a-i) were readily obtained by the treatment of 4a-i with hydrochloric acid and were finally led to N-methylated products (6a-I) with methyl iodide. The reduction of maleimides (4-6) with zinc dust in acetic acid afforded the corresponding 3-arylpyrrolidine-2,5-diones (7a-i) that can be converted to pharmacologycally active compounds like mesembrines.
    DOI:
    10.3987/com-01-9336
  • 作为产物:
    参考文献:
    名称:
    Synthesis of 3-Methylthio-4-aryl-3-pyrroline-2,5-diones and 3-Arylpyrrolidine-2,5-diones by Reaction of Nitroketene Dithioacetal with Arylacetonitriles
    摘要:
    The reaction of nitroketene dithioacetal (1a), i.e., 2,2-bis(methylthio)-1-nitroethylene, with arylacetonitriles (2a-I) in the presence of the base like sodium hydroxide gave 4-nitrobut-2-enenitriles (3a-I) which were converted into 5-hydroxyimino-4-methylthio-3-phenyl-3-pyrrolin-2-ones (4a-i) under refluxing in methanol. Title compounds (5a-i) were readily obtained by the treatment of 4a-i with hydrochloric acid and were finally led to N-methylated products (6a-I) with methyl iodide. The reduction of maleimides (4-6) with zinc dust in acetic acid afforded the corresponding 3-arylpyrrolidine-2,5-diones (7a-i) that can be converted to pharmacologycally active compounds like mesembrines.
    DOI:
    10.3987/com-01-9336
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文献信息

  • Diverse 3-Methylthio-4-Substituted Maleimides through a Novel Rearrangement Reaction: Synthesis and Selective Cell Imaging
    作者:Luan V. Meirelles、Pedro P. de Castro、Saulo T. A. Passos、Bernardo B. P. P. Carvalho、Chris H. J. Franco、José R. Correa、Brenno A. D. Neto、Giovanni W. Amarante
    DOI:10.1021/acs.joc.1c02714
    日期:2022.3.4
    metal-free protocol for the preparation of fluorescent and non-fluoresent 3-methylthio-4-arylmaleimides in a single step through a new rearrangement from thiazolidine-2,4-diones is described. By employing the optimized reaction conditions, a broad scope of derivatives was prepared in ≤97% yield. The reaction tolerated several substituted aryl groups, including the challenging preparation of pyridyl-containing
    描述了通过从 thiazolidine-2,4-diones 进行新的重排,一步制备荧光和非荧光 3-methylthio-4-arylmaleimides 的无过渡属协议。通过采用优化的反应条件,以≤97%的收率制备了广泛的衍生物。该反应耐受几个取代的芳基,包括具有挑战性的含吡啶基衍生物的制备。一系列对照实验强烈表明新的重排涉及关键的异氰酸酯中间体和与原位生成的甲基代甲基乙酸酯的进一步反应。还研究了一些合成衍生物的光物理性质及其在活细胞成像中的用途,
  • Convergent integration of three self-sorting domino sequences: three-component direct synthesis of 3-methylthio-4-aryl-maleimides from methyl ketones with acetonitrile and DMSO
    作者:Qinghe Gao、Shan Liu、Xia Wu、Anxin Wu
    DOI:10.1016/j.tetlet.2014.09.099
    日期:2014.11
    converted to DMS in situ, which subsequently served as a methylthiolation reagent in the reaction. To the best of our knowledge, this protocol provided the first known example of convergent integration of three self-sorting domino sequences.
    描述了由I 2促进的三组分偶联反应,用于由甲基酮与乙腈DMSO构建3-(甲基)-4-芳基-1 H-吡咯-2,5-二酮。该转化涉及α-酮酰亚胺的原位产生和应用。此外,DMSO原位转化为DMS,随后在反应中用作甲基醇化试剂。据我们所知,该协议提供了三个自排序多米诺骨牌序列的融合整合的第一个已知示例。
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