2-(7-Methyl-1-benzofuran-2-yl)acetaldehyde | 1599313-41-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并呋喃
• 英文名称: 2-(7-Methyl-1-benzofuran-2-yl)acetaldehyde
• 英文别名: 2-(7-methyl-1-benzofuran-2-yl)acetaldehyde
• CAS: 1599313-41-3
• 化学式: C₁₁H₁₀O₂
• 分子量: 174.199
• InChiKey: SPQHHOABAGFWBX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  30.2
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(7-Methyl-1-benzofuran-2-yl)acetaldehyde 、 苯甲酰基亚甲基三苯基膦 以 四氢呋喃 为溶剂， 反应 3.0h， 生成 (E)-4-(7-methylbenzofuran-2-yl)-1-phenylbut-2-en-1-one
  参考文献：
  名称：

  Asymmetric Dearomatic Diels–Alder Reactions of Diverse Heteroarenes via π-System Activation

  摘要：

  An asymmetric dearomatic Diels-Alder protocol for various heteroarenes, such as benzofuran, benzothiophene, or even furan, has been developed via pi-system activation. This method involves in situ generation of formal trienamine species embedding a heteroaromatic moiety, and an array of chiral fused frameworks with high molecular complexity and skeletal diversity were efficiently constructed in good to excellent stereoselectivity by the catalysis of a cinchona-based primary amine.

  DOI：

  10.1021/ol501217u
• 作为产物：
  描述：

  氯乙酸甲酯 、 7-甲基-1-苯并呋喃-2-甲醛 在 sodium 、 potassium hydroxide 、 potassium dihydrogenphosphate 、 水 作用下， 以 甲醇 、 水 、 二氯甲烷 为溶剂， 反应 7.0h， 生成 2-(7-Methyl-1-benzofuran-2-yl)acetaldehyde
  参考文献：
  名称：

  Asymmetric Dearomatic Diels–Alder Reactions of Diverse Heteroarenes via π-System Activation

  摘要：

  An asymmetric dearomatic Diels-Alder protocol for various heteroarenes, such as benzofuran, benzothiophene, or even furan, has been developed via pi-system activation. This method involves in situ generation of formal trienamine species embedding a heteroaromatic moiety, and an array of chiral fused frameworks with high molecular complexity and skeletal diversity were efficiently constructed in good to excellent stereoselectivity by the catalysis of a cinchona-based primary amine.

  DOI：

  10.1021/ol501217u

文献信息

• [EN] NEW ARYLALKENYLPROPARGYLAMINE DERIVATIVES EXHIBITING NEUROPROTECTIVE ACTION FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES<br/>[FR] NOUVEAUX DÉRIVÉS ARYLALCÉNYLPROPARGYLAMINE FAISANT PREUVE D'ACTION NEUROPROTECTRICE POUR LE TRAITEMENT DES MALADIES NEURODÉGÉNÉRATIVES
  申请人：SEMMELWEIS EGYETEM

  公开号：WO2015087094A1

  公开（公告）日：2015-06-18

  The invention relates to novel arylalkenylpropargylamine derivatives of general formula (I) or enantiomers or diastereomers thereof or salts, optionally pharmaceutically acceptable salts, or solvates of any of these. The compounds can be used in treating or preventing a disease or condition in a mammal related to monoamine oxidase dysfunction, especially in neurodegenerative diseases, e.g. Parkinson's disease, Alzheimer's disease or Huntington's disease.

  本发明涉及一类新型的芳基烯丙炔丙胺衍生物，其具有通用公式（I）或其对应的手性异构体或对映异构体或盐，可选用药物上可接受的盐，或者这些化合物的溶剂化物。这些化合物可用于治疗或预防哺乳动物与单胺氧化酶功能障碍相关的疾病或状况，特别是在神经退行性疾病中，例如帕金森病、阿尔茨海默病或亨廷顿病。
• Asymmetric Dearomatic Diels–Alder Reactions of Diverse Heteroarenes via π-System Activation
  作者：You-Cai Xiao、Cai-Zhen Yue、Peng-Qiao Chen、Ying-Chun Chen

  DOI：10.1021/ol501217u

  日期：2014.6.20

  An asymmetric dearomatic Diels-Alder protocol for various heteroarenes, such as benzofuran, benzothiophene, or even furan, has been developed via pi-system activation. This method involves in situ generation of formal trienamine species embedding a heteroaromatic moiety, and an array of chiral fused frameworks with high molecular complexity and skeletal diversity were efficiently constructed in good to excellent stereoselectivity by the catalysis of a cinchona-based primary amine.