Isopropylhex-5-en-1-amine | 1314913-55-7

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: Isopropylhex-5-en-1-amine
• 英文别名: 2-Methyloct-7-en-3-amine
• CAS: 1314913-55-7
• 化学式: C₉H₁₉N
• 分子量: 141.257
• InChiKey: WESXXXHDFXDQPX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  10
• 可旋转键数：
  5
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  Isopropylhex-5-en-1-amine 在 Hoveyda-Grubbs catalyst second generation 、 sodium carbonate 作用下， 以 乙醚 、 水 为溶剂， 反应 18.0h， 生成
  参考文献：
  名称：

  Iron-Catalyzed Synthesis of α-Dienyl Five- and Six-Membered N-Heterocycles

  摘要：

  The iron‐catalyzed synthesis of α‐dienyl N‐heterocycles is reported. The method is cost‐effective, atom‐economic, and led to a range of substituted α‐dienyl heterocycles in moderate to good yields and diastereoselectivities. The α‐dienyl piperidines are key synthetic intermediates as demonstrated by the preparation of a panel of α‐polyenyl N‐heterocycles.

  DOI：

  10.1002/ejoc.201700977
• 作为产物：
  描述：

  5-己烯醛 在 甲酸铵 、 pyridinium chlorochromate 作用下， 以 甲醇 、 乙醚 、 二氯甲烷 为溶剂， 反应 5.5h， 生成 Isopropylhex-5-en-1-amine
  参考文献：
  名称：

  Iron-Catalyzed Synthesis of α-Dienyl Five- and Six-Membered N-Heterocycles

  摘要：

  The iron‐catalyzed synthesis of α‐dienyl N‐heterocycles is reported. The method is cost‐effective, atom‐economic, and led to a range of substituted α‐dienyl heterocycles in moderate to good yields and diastereoselectivities. The α‐dienyl piperidines are key synthetic intermediates as demonstrated by the preparation of a panel of α‐polyenyl N‐heterocycles.

  DOI：

  10.1002/ejoc.201700977

文献信息

• HCV NS3 Protease Inhibitors
  申请人：Liverton Nigel J.

  公开号：US20100317623A1

  公开（公告）日：2010-12-16

  The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.

  本发明涉及式（I）的大环化合物，其作为丙型肝炎病毒（HCV）NS3蛋白酶的抑制剂，它们的合成以及它们用于治疗或预防HCV感染的用途。
• FeCl₃-Catalyzed Highly Diastereoselective Synthesis of Substituted Piperidines and Tetrahydropyrans
  作者：Amandine Guérinot、Anna Serra-Muns、Christian Gnamm、Charlélie Bensoussan、Sébastien Reymond、Janine Cossy

  DOI：10.1021/ol100422d

  日期：2010.4.16

  The eco-friendly and highly diastereoselective synthesis of substituted cis-2,6-piperidines and cis-2,6-tetrahydropyrans is described. The key step of this method is the iron-catalyzed thermodynamic equilibration of 2-alkenyl 6-substituted piperidines and 2-alkenyl 6-substituted tetrahydropyrans allowing the isolation of enriched mixtures of the most stable cis-isomers.
• US8138164B2
  申请人：——

  公开号：US8138164B2

  公开（公告）日：2012-03-20
• Iron-Catalyzed Synthesis of α-Dienyl Five- and Six-Membered N-Heterocycles
  作者：Laurine Gonnard、Amandine Guérinot、Janine Cossy

  DOI：10.1002/ejoc.201700977

  日期：2017.11.9

  The iron‐catalyzed synthesis of α‐dienyl N‐heterocycles is reported. The method is cost‐effective, atom‐economic, and led to a range of substituted α‐dienyl heterocycles in moderate to good yields and diastereoselectivities. The α‐dienyl piperidines are key synthetic intermediates as demonstrated by the preparation of a panel of α‐polyenyl N‐heterocycles.