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(S)-1-methyl-3-(2-(methylthio)ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

中文名称
——
中文别名
——
英文名称
(S)-1-methyl-3-(2-(methylthio)ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione
英文别名
(3S)-1-methyl-3-(2-methylsulfanylethyl)-3,4-dihydro-1,4-benzodiazepine-2,5-dione
(S)-1-methyl-3-(2-(methylthio)ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione化学式
CAS
——
化学式
C13H16N2O2S
mdl
——
分子量
264.348
InChiKey
MWYCNRQMMIBKGY-JTQLQIEISA-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):
    1.4
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    74.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (S)-1-methyl-3-(2-(methylthio)ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione4-二甲氨基吡啶双(三甲基硅烷基)氨基钾三乙胺 作用下, 以 四氢呋喃甲苯 为溶剂, 反应 13.0h, 生成 tert-butyl (R)-(1-methyl-3-(2-(methylthio)ethyl)-2,4-dioxo-1,2,3,4-tetrahydroquinolin-3-yl)carbamate
    参考文献:
    名称:
    Enantioselective Deprotonative Ring Contraction of N1-Methyl-N4-Boc-benzo[e][1,4]diazepine-2,5-diones
    摘要:
    N1-Methyl-N4-Boc-benzo[e][1,4] diazepine 2,5-diones were prepared in good yield an high stereo chemical purity from five amino acids Upon deprotonation these compounds undergo ring contraction to the corresponding quinolone 2,4-diones withhigh enantioselectivity, providing efficient entry to a potentially useful drug scaffold Mechanistic commentary and comparisons to related reactions are provided.
    DOI:
    10.1021/ol502586n
  • 作为产物:
    描述:
    L-蛋氨酸1-甲基苯唑溶剂黄146 作用下, 反应 18.0h, 以60%的产率得到(S)-1-methyl-3-(2-(methylthio)ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione
    参考文献:
    名称:
    Enantioselective Deprotonative Ring Contraction of N1-Methyl-N4-Boc-benzo[e][1,4]diazepine-2,5-diones
    摘要:
    N1-Methyl-N4-Boc-benzo[e][1,4] diazepine 2,5-diones were prepared in good yield an high stereo chemical purity from five amino acids Upon deprotonation these compounds undergo ring contraction to the corresponding quinolone 2,4-diones withhigh enantioselectivity, providing efficient entry to a potentially useful drug scaffold Mechanistic commentary and comparisons to related reactions are provided.
    DOI:
    10.1021/ol502586n
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