N-(dimethylsulfamoyl)cinnamaldehyde | 764660-93-7

• 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: N-(dimethylsulfamoyl)cinnamaldehyde
• CAS: 764660-93-7
• 化学式: C₁₁H₁₄N₂O₂S
• 分子量: 238.31
• InChiKey: YRPRMTKPFVOJIO-IZSRKLPESA-N

物化性质

• 沸点：
  376.6±35.0 °C(Predicted)
• 密度：
  1.10±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.58
• 重原子数：
  16.0
• 可旋转键数：
  4.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  49.74
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  烯丙基三丁基锡 、 N-(dimethylsulfamoyl)cinnamaldehyde 在 resorcinolbis[(diphenyl)phosphinite] palladium trifluoroacetate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 16.0h， 以68%的产率得到
  参考文献：
  名称：

  P′CP′-Pincer palladium complex-catalyzed allylation of N,N-dimethylsulfamoyl-protected aldimines

  摘要：

  The P'CP'-pincer palladium complex-catalyzed allylation of N,N-dimethylsulfamoyl-protected aldimines with allyl(tributyl)stannane is investigated for the preparation of N-homoallylic sulfamides. The desired N,N-dimethylsulfamoyl-protected products are obtained in moderate to high yields in DMF under very mild conditions and a high yielding and convenient deprotection of the N,N-dimethylsulfamoyl group is also demonstrated. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2009.02.187
• 作为产物：
  描述：

  反式肉桂醛 、 N,N-二甲基磺酰胺 以 水 、 甲苯 为溶剂， 反应 16.0h， 生成 N-(dimethylsulfamoyl)cinnamaldehyde
  参考文献：
  名称：

  P′CP′-Pincer palladium complex-catalyzed allylation of N,N-dimethylsulfamoyl-protected aldimines

  摘要：

  The P'CP'-pincer palladium complex-catalyzed allylation of N,N-dimethylsulfamoyl-protected aldimines with allyl(tributyl)stannane is investigated for the preparation of N-homoallylic sulfamides. The desired N,N-dimethylsulfamoyl-protected products are obtained in moderate to high yields in DMF under very mild conditions and a high yielding and convenient deprotection of the N,N-dimethylsulfamoyl group is also demonstrated. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2009.02.187

文献信息

• Novel synthesis of 4(5)-monosubstituted imidazoles via cycloaddition of tosylmethyl isocyanide to aldimines
  作者：Ronald ten Have、Marco Huisman、Auke Meetsma、Albert M van Leusen

  DOI：10.1016/s0040-4020(97)00717-5

  日期：1997.8

  4(5)-Monosubstituted imidazoles (9) have been prepared via base-induced cycloaddition of tosylmethyl isocyanide (TosMIC) to N-(dimethylsulfamoyl)aldimines (2) or N-tosylaldimines (3). In the first case, N-(dimethylsulfamoyl)imidazoles 8 are the initial reaction products, from which the dimethylsulfamoyl group is readily removed with aqueous HBr. In the second case, the tosyl group of 1-tosylimidazoles

  4（5）-单取代的咪唑（9）是通过将甲苯磺酰基甲基异氰化物（TosMIC）与N-（二甲基氨磺酰基）醛亚胺（2）或N-甲苯磺酰基亚胺（3）进行碱诱导的环加成而制备的。在第一种情况下，N-（二甲基氨磺酰基）咪唑8是初始反应产物，可以用HBr水溶液很容易地从中除去二甲基氨磺酰基。在第二种情况下，在一个操作中，1-甲苯基咪唑10的甲苯磺酰基自发地丢失，得到4（5）-单取代的咪唑9。