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2-deuterio-3,5-bis(phenylsulfonyl)-1-benzyl-2-phenyl-1,2,5,6-tetrahydropyridine | 133167-15-4

中文名称
——
中文别名
——
英文名称
2-deuterio-3,5-bis(phenylsulfonyl)-1-benzyl-2-phenyl-1,2,5,6-tetrahydropyridine
英文别名
——
2-deuterio-3,5-bis(phenylsulfonyl)-1-benzyl-2-phenyl-1,2,5,6-tetrahydropyridine化学式
CAS
133167-15-4
化学式
C30H27NO4S2
mdl
——
分子量
530.673
InChiKey
CTWWMGFTISMBBL-KHRVYUSUSA-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):
    5.44
  • 重原子数:
    37.0
  • 可旋转键数:
    7.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    71.52
  • 氢给体数:
    0.0
  • 氢受体数:
    5.0

反应信息

  • 作为产物:
    参考文献:
    名称:
    Formation of polysubstituted 1,2,5,6-tetrahydropyridines from the 4+2 cycloaddition reaction of bis(phenylsulfonyl)butadienes with aryl imines
    摘要:
    The reaction of 2,3-bis(phenylsulfonyl)-1,3-butadiene with aryl imines affords N-alkyl-3,5-bis(phenylsulfonyl)-1,2,5,6-tetrahydropyridines in high yield. The formation of the rearranged cycloadducts proceeds by a mechanism that involves addition of benzenesulfinate anion onto the terminal pi-bond of the activated diene. The resulting carbanion undergoes proton transfer followed by aryl sulfinate ejection to give 1,3-bis(phenylsulfonyl)-1,3-butadiene as a transient intermediate. This reactive diene undergoes a rapid 4 + 2 cycloaddition followed by a subsequent hydrogen 1,3-shift. Support for the proposed mechanism is provided by the observation that a mixed cycloadduct is obtained from the reaction of a 1:1 mixture of 2,3-bis(phenylsulfonyl)- and 2,3-bis[(o-nitrophenyl)sulfonyl]butadiene with N-benzylidenemethylamine. An additional piece of supporting data for the proposed mechanism is the much shorter reaction time necessary for the reaction to go to completion when a small amount of sodium benzenesulfinate is added to the reaction mixture. 1,3-Bis(phenylsulfonyl)butadiene was independently synthesized by two different routes. This diene was found to rapidly react with a variety of imines to give the same cycloadducts as those derived from the 2,3-isomer. The reaction of several 4-substituted 1,3-bis(phenylsulfonyl)butadienes with aryl imines was found to give related 4 + 2 cycloadducts.
    DOI:
    10.1021/jo00008a026
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