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2-thiaspiro[3.5]nonan-1-one | 1146929-20-5

中文名称
——
中文别名
——
英文名称
2-thiaspiro[3.5]nonan-1-one
英文别名
2-Thiaspiro[3.5]nonan-3-one
2-thiaspiro[3.5]nonan-1-one化学式
CAS
1146929-20-5
化学式
C8H12OS
mdl
——
分子量
156.249
InChiKey
XWOWFCPGZJUMAY-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:
    286.5±9.0 °C(Predicted)
  • 密度:
    1.15±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-thiaspiro[3.5]nonan-1-one2,4-二硝基氟苯2-苯乙胺caesium carbonate4-氯苯硫酚 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以80%的产率得到1-[(2,4-dinitrophenylsulfanyl)methyl]-N-phenethylcyclohexanecarboxamide
    参考文献:
    名称:
    βN-硫代内酯(硫丹-2-酮)的S N 2型亲核开环作为偶联反应的硫代酸来源
    摘要:
    在3位上被烷基和氨基甲酰基单取代的β-硫内酯通过涉及S N的过程被芳硫醇盐进行亲核开环在4位上发生2型攻击,导致在3位上取代了3-芳基硫代丙酸酯。这些硫代羧酸盐可以通过亲山芳烃取代过程由Mukaiyama试剂或Sanger试剂原位捕获,从而导致高度活化的硫酯,然后使它们与伯胺或仲胺进一步反应,总体上导致一锅,三组分合成在2-位带有各种取代基的3-芳基硫代丙酰胺。或者,可用2,4-二硝基苯磺酰胺代替电子不足的芳基卤化物和胺的捕集组合,导致整体形成相同的产物,同时在磺酰胺中掺入潜伏胺到最终的酰胺产物中。在另一个实施例中,N-芳烃磺酰基3-芳基硫代丙酰胺衍生物。
    DOI:
    10.1021/jo9001728
  • 作为产物:
    描述:
    1-(mercaptomethyl)cyclohexanecarboxylic acid三乙胺氯甲酸异丁酯 作用下, 以 二氯甲烷 为溶剂, 反应 0.75h, 以1.08 g的产率得到2-thiaspiro[3.5]nonan-1-one
    参考文献:
    名称:
    βN-硫代内酯(硫丹-2-酮)的S N 2型亲核开环作为偶联反应的硫代酸来源
    摘要:
    在3位上被烷基和氨基甲酰基单取代的β-硫内酯通过涉及S N的过程被芳硫醇盐进行亲核开环在4位上发生2型攻击,导致在3位上取代了3-芳基硫代丙酸酯。这些硫代羧酸盐可以通过亲山芳烃取代过程由Mukaiyama试剂或Sanger试剂原位捕获,从而导致高度活化的硫酯,然后使它们与伯胺或仲胺进一步反应,总体上导致一锅,三组分合成在2-位带有各种取代基的3-芳基硫代丙酰胺。或者,可用2,4-二硝基苯磺酰胺代替电子不足的芳基卤化物和胺的捕集组合,导致整体形成相同的产物,同时在磺酰胺中掺入潜伏胺到最终的酰胺产物中。在另一个实施例中,N-芳烃磺酰基3-芳基硫代丙酰胺衍生物。
    DOI:
    10.1021/jo9001728
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文献信息

  • SUBSTITUTED 4-ALKOXYPICOLINAMIDE ANALOGS AS MGLUR5 NEGATIVE ALLOSTERIC MODULATORS AND METHODS OF MAKING AND USING THE SAME
    申请人:VANDERBILT UNIVERSITY
    公开号:US20170247366A1
    公开(公告)日:2017-08-31
    Disclosed are negative allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with glutamate dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
  • [EN] SUBSTITUTED 4-ALKOXYPICOLINAMIDE ANALOGS DS MGLUR5 NEGATIVE ALLOSTERIC MODULATORS<br/>[FR] ANALOGUES SUBSTITUÉS DE 4-ALCOXYPICOLINAMIDE EN TANT QUE MODULATEURS ALLOSTÉRIQUES NÉGATIFS DE MGLUR5
    申请人:UNIV VANDERBILT
    公开号:WO2015200682A1
    公开(公告)日:2015-12-30
    Disclosed are negative allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5); synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with glutamate dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
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