1-cyclopropyl-3,3-dimethyl-1-(1-phenylpent-3-yn-1-yl)urea | 1428157-06-5

• 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: 1-cyclopropyl-3,3-dimethyl-1-(1-phenylpent-3-yn-1-yl)urea
• CAS: 1428157-06-5
• 化学式: C₁₇H₂₂N₂O
• 分子量: 270.374
• InChiKey: NREWSDZPFBVYTK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.29
• 重原子数：
  20.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  23.55
• 氢给体数：
  0.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  一氧化碳 、 1-cyclopropyl-3,3-dimethyl-1-(1-phenylpent-3-yn-1-yl)urea 在 bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate 、 三[3,4-双(三氟甲基)苯基]膦 作用下， 以 苯甲腈 为溶剂， 130.0 ℃ 、101.33 kPa 条件下， 反应 24.0h， 以45%的产率得到N,N,4-trimethyl-5-oxo-2-phenyl-2,3,5,6,7,7a-hexahydro-1H-indole-1-carboxamide
  参考文献：
  名称：

  Directed carbonylative (3+1+2) cycloadditions of amino-substituted cyclopropanes and alkynes: reaction development and increased efficiencies using a cationic rhodium system

  摘要：

  Urea-directed carbonylative insertion of Rh(I)-catalysts into one of the two proximal C-C bonds of aminocyclopropanes generates rhodacyclopentanone intermediates. These are trapped by N-tethered alkynes to provide a (3+1+2) cycloaddition protocol that accesses N-heterobicyclic enones. Stoichiometric studies on a series of model rhodacyclopentanone complexes outline key structural features and provide a rationale for the efficacy of urea directing groups. A comprehensive evaluation of cycloaddition scope and a 'second generation' cationic Rh(I)-system, which provides enhanced yields and reaction rates for challenging substrates, are presented. (C) 2015 The Authors. Published by Elsevier Ltd.

  DOI：

  10.1016/j.tet.2015.08.052
• 作为产物：
  描述：

  苯甲醛 在 正丁基锂 、 1,2-二碘乙烷 、 magnesium sulfate 、 三乙胺 、 锌 作用下， 以 四氢呋喃 、 正己烷 、 二氯甲烷 、 甲苯 为溶剂， 反应 121.5h， 生成 1-cyclopropyl-3,3-dimethyl-1-(1-phenylpent-3-yn-1-yl)urea
  参考文献：
  名称：

  Directing Group Enhanced Carbonylative Ring Expansions of Amino-Substituted Cyclopropanes: Rhodium-Catalyzed Multicomponent Synthesis of N-Heterobicyclic Enones

  摘要：

  Aminocyclopropanes equipped with suitable N-directing groups undergo efficient and regioselective Rh-catalyzed carbonylative C-C bond activation. Trapping of the resultant metallacycles with tethered alkynes provides an atom-economic entry to diverse N-heterobicyclic enones. These studies provide a blueprint for myriad N-heterocyclic methodologies.

  DOI：

  10.1021/ja401936c