7,8-dimethoxy-6'-oxospiro[3,4-dihydro-1H-2-benzazepine-5,3'-cyclohexa-1,4-diene]-2-carbaldehyde | 717865-67-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯氮卓类
• 英文名称: 7,8-dimethoxy-6'-oxospiro[3,4-dihydro-1H-2-benzazepine-5,3'-cyclohexa-1,4-diene]-2-carbaldehyde
• CAS: 717865-67-3
• 化学式: C₁₈H₁₉NO₄
• 分子量: 313.353
• InChiKey: IVYALXPDDROXBU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  23
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  55.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  7,8-dimethoxy-6'-oxospiro[3,4-dihydro-1H-2-benzazepine-5,3'-cyclohexa-1,4-diene]-2-carbaldehyde 在 palladium diacetate 吡啶 、 甲酸 、 甲烷磺酸 、 三乙胺 、 三苯基膦 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 80.0h， 生成 N-formyl-2,3-dimethoxy-5,6,7,8-tetrahydrodiben[c,e]azocine
  参考文献：
  名称：

  Synthesis of Amaryllidaceae alkaloids, siculine, oxocrinine, epicrinine, and buflavine

  摘要：

  Three crinane type of alkaloids isolated from Amaryllidaceae family were synthesized by taking advantage of the PIFA-mediated intramolecular p-p' diphenol coupling reaction of norbelladine derivatives. Furthermore, buflavine was also prepared by using the p-p' diphenol coupling followed by dienone-phenol rearrangement as a key step. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2004.03.087
• 作为产物：
  描述：

  对羟基苯乙胺 在 2,2,2-三氟乙醇 、 [双(三氟乙酰氧基)碘]苯 作用下， 以 甲醇 为溶剂， 反应 34.5h， 生成 7,8-dimethoxy-6'-oxospiro[3,4-dihydro-1H-2-benzazepine-5,3'-cyclohexa-1,4-diene]-2-carbaldehyde
  参考文献：
  名称：

  Synthesis of Amaryllidaceae alkaloids, siculine, oxocrinine, epicrinine, and buflavine

  摘要：

  Three crinane type of alkaloids isolated from Amaryllidaceae family were synthesized by taking advantage of the PIFA-mediated intramolecular p-p' diphenol coupling reaction of norbelladine derivatives. Furthermore, buflavine was also prepared by using the p-p' diphenol coupling followed by dienone-phenol rearrangement as a key step. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2004.03.087

文献信息

• A General Electro‐Synthesis Approach to Amaryllidaceae Alkaloids
  作者：Dennis Pollok、Luca M. Großmann、Torsten Behrendt、Till Opatz、Siegfried R. Waldvogel

  DOI：10.1002/chem.202201523

  日期：2022.9.6

  Highly pharmaceutically relevant Amaryllidaceae alkaloids have been accessed by a versatile electro-organic key transformation, including a precursor of the acetylcholinesterase inhibitor galantamine, used as FDA-approved drug for the treatment of Alzheimer's disease. Spirodienone-type intermediates were obtained in a regioselective and sustainable anodic key transformation from nature-derived starting

  高度药学相关的石蒜科生物碱已通过多功能电有机关键转化获得，其中包括乙酰胆碱酯酶抑制剂加兰他敏的前体，该药物被 FDA 批准用作治疗阿尔茨海默病的药物。螺二烯酮型中间体是通过区域选择性和可持续的阳极关键转化从天然原料中获得的