(2S,4R,5S)-4-(methoxycarbonylmethyl)-2-methyl-5-phenyl-1-(p-toluenesulfonyl)piperidine | 1254356-13-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (2S,4R,5S)-4-(methoxycarbonylmethyl)-2-methyl-5-phenyl-1-(p-toluenesulfonyl)piperidine
• 英文别名: methyl 2-[(2S,4R,5S)-2-methyl-1-(4-methylphenyl)sulfonyl-5-phenylpiperidin-4-yl]acetate
• CAS: 1254356-13-2
• 化学式: C₂₂H₂₇NO₄S
• 分子量: 401.527
• InChiKey: UZSJKAXXHGCGKH-FBBABVLZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  72.1
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  (3S)-(p-toluenesulfonyl)amino-butyronitrile 在 偶氮二异丁腈 、 三正丁基氢锡 、 三溴化磷 、 二异丁基氢化铝 、 caesium carbonate 作用下， 以 二氯甲烷 、 甲苯 、 乙腈 为溶剂， 反应 54.75h， 生成 (2S,4R,5S)-4-(methoxycarbonylmethyl)-2-methyl-5-phenyl-1-(p-toluenesulfonyl)piperidine 、 (2S,4S,5S)-4-(methoxycarbonylmethyl)-2-methyl-5-phenyl-1-(p-toluenesulfonyl)piperidine
  参考文献：
  名称：

  Stereoselective Synthesis of 2,4,5-Trisubstituted Piperidines via Radical Cyclization

  摘要：

  A novel approach to 2,4,5-trisubstituted piperidines is reported, involving the 6-exo cyclization of stabilized radicals onto alpha,beta-unsaturated esters. Only two of the four possible diastereoisomers are observed, with diastereomeric ratios ranging from 3:2 to 40:1 when the radical stabilizing group is vinyl or phenyl. Cyclization of a (triethylsilyl)vinyl-stabilized radical gives the corresponding piperidine radical as a single diastereoisomer that may either be trapped by tributyltin hydride to afford the 2,4,5-trisubstituted piperidine or undergo a second 5-endo cyclization onto the (triethylsilyl)vinyl substituent to produce the 3,5,7-trisubstituted octahydro[2]pyrindene as a single diastereoisomer.

  DOI：

  10.1021/jo101631y

文献信息

• Stereoselective Synthesis of 2,4,5-Trisubstituted Piperidines via Radical Cyclization
  作者：Maria-Eleni Ragoussi、Stephen M. Walker、Andrea Piccanello、Benson M. Kariuki、Peter N. Horton、Neil Spencer、John S. Snaith

  DOI：10.1021/jo101631y

  日期：2010.11.5

  A novel approach to 2,4,5-trisubstituted piperidines is reported, involving the 6-exo cyclization of stabilized radicals onto alpha,beta-unsaturated esters. Only two of the four possible diastereoisomers are observed, with diastereomeric ratios ranging from 3:2 to 40:1 when the radical stabilizing group is vinyl or phenyl. Cyclization of a (triethylsilyl)vinyl-stabilized radical gives the corresponding piperidine radical as a single diastereoisomer that may either be trapped by tributyltin hydride to afford the 2,4,5-trisubstituted piperidine or undergo a second 5-endo cyclization onto the (triethylsilyl)vinyl substituent to produce the 3,5,7-trisubstituted octahydro[2]pyrindene as a single diastereoisomer.