9-(bromomethyl)-2,3,6,7-tetramethoxyphenanthrene | 1150647-83-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 菲及其衍生物
• 英文名称: 9-(bromomethyl)-2,3,6,7-tetramethoxyphenanthrene
• CAS: 1150647-83-8
• 化学式: C₁₉H₁₉BrO₄
• 分子量: 391.261
• InChiKey: RBQVETBRSFPPGP-UHFFFAOYSA-N

物化性质

• 熔点：
  195-197 °C(Solv: benzene (71-43-2))
• 沸点：
  513.3±45.0 °C(Predicted)
• 密度：
  1.381±0.06 g/cm3(Predicted)
• 溶解度：
  溶于氯仿

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  24
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  36.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  9-(bromomethyl)-2,3,6,7-tetramethoxyphenanthrene 在 盐酸 、 正丁基锂 、 二异丙胺 作用下， 以 四氢呋喃 、 乙醇 、 水 为溶剂， 反应 21.33h， 生成 methyl 2,3,6,7-tetramethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline-13a-carboxylate
  参考文献：
  名称：

  Design, synthesis, antiviral activity, and SARs of 13a-substituted phenanthroindolizidine alkaloid derivatives

  摘要：

  On the basis of our previous structure-activity relationship (SAR) and antiviral mechanism studies, a series of 13a-substituted phenanthroindolizidine alkaloid analogues (3a-16a, 3b, 4b, 6b, 7b, 10b, and 14b) were designed targeting tobacco mosaic virus (TMV) RNA, synthesized, and evaluated for their antiviral activity against TMV for the first time. The bioassay results showed that most of the synthesized compounds (such as 4a, 6a, 7a, 11a, 14a, 6b, and 14b) exhibited good to excellent antiviral activity against TMV both in vitro and in vivo. Especially, for inactivation effect and curative effect, compounds 4a, 6a, 7a, 11a, 14a, and 14b showed higher activity at both concentrations (500 mu g mL(-1) and 100 mu g mL(-1)) than commercial Ningnanmycin. Preliminary SARs showed that the substituted groups with hydrogen donor at 13a position were found to be favorable for keeping high antiviral activity. The present work demonstrates that 13a-substituted phenanthroindolizidines can be used as possible lead compounds for developing anti-TMV agents. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2014.04.101
• 作为产物：
  描述：

  methyl (E)-2,3-bis(3,4-dimethoxyphenyl)acrylate 在 lithium aluminium tetrahydride 、 甲烷磺酸 、 三溴化磷 、 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 16.5h， 生成 9-(bromomethyl)-2,3,6,7-tetramethoxyphenanthrene
  参考文献：
  名称：

  N,N-二苄基氨基乙腈连续烷基化全合成苯哌啶类生物碱

  摘要：

  Tylophorine 和 cryptopleurine 是通过金属化的 α-氨基腈与溴甲基菲缩合得到完全取代的 α-氨基腈合成的，然后进行还原脱氰以形成高苄胺。从这些中间体中，分别通过末端离去基团的置换和晚期 Pictet-Spengler 缩合形成 tylophorine 和 cryptopleurine 的 E 和 D 环。

  DOI：

  10.1002/ejoc.202101131

文献信息

• Collective Asymmetric Synthesis of (−)-Antofine, (−)-Cryptopleurine, (−)-Tylophorine, and (−)-Tylocrebrine with <i>tert-</i>Butanesulfinamide as a Chiral Auxiliary
  作者：Yanlong Zheng、Yuxiu Liu、Qingmin Wang

  DOI：10.1021/jo500013e

  日期：2014.4.18

  A collective asymmetric synthesis of phenanthroindolizidine and phenanthroquinolizidine alkaloids (−)-antofine, (−)-cryptopleurine, (−)-tylophorine, and (−)-tylocrebrine was achieved by means of a reaction sequence involving efficient generation of chiral homoallylic amine intermediates by asymmetric allylation of the corresponding tert-butanesulfinyl imine. From these intermediates, the pyrrolidine

  菲咯啉吲哚和菲咯啉喹嗪生物碱（-）-antofine，（-）-cryptopleurine，（-）-酪氨酸和（-）-酪蛋白的集体不对称合成是通过涉及通过有效生成手性均烯丙基胺中间体的反应序列实现的对应的叔丁烷亚磺酰基亚胺的不对称烯丙基化。从这些中间体，吡咯烷和哌啶环通过分子内S的装置构造Ñ分别2取代反应和闭环复分解反应，。是由一个的InCl的装置产生tylocrebrine - （ - ）的不寻常的C5-甲氧基取代的菲部分3的催化的的反应环异构ø -炔丙基二芳基化合物。
• D and E Rings May Not Be Indispensable for Antofine: Discovery of Phenanthrene and Alkylamine Chain Containing Antofine Derivatives as Novel Antiviral Agents against Tobacco Mosaic Virus (TMV) Based on Interaction of Antofine and TMV RNA
  作者：Ziwen Wang、Peng Wei、Yuxiu Liu、Qingmin Wang

  DOI：10.1021/jf5028894

  日期：2014.10.29

  (TMV) RNA, a series of phenanthrene and alkylamine chain containing antofine derivatives 1–41 were designed, synthesized, and systematically evaluated for their antiviral activity against TMV. The results showed that most of these compounds exhibited good to excellent anti-TMV activity, which indicated that the D and E rings of antofine may not be indispensable. Phenanthrene is important for these

  在antofine和烟草花叶病毒（TMV）RNA相互作用的基础上，设计，合成了一系列包含菲和烷基胺链的antofine衍生物1 – 41，并系统地评估了它们对TMV的抗病毒活性。结果表明，这些化合物中的大多数都表现出良好至优异的抗TMV活性，这表明antofine的D和E环可能不是必不可少的。菲对这些化合物很重要，但越多越好。菲，苯环和含烷基胺链的化合物表现出良好的抗病毒活性。最佳化合物，10，18，和19与前体antofine和市售利巴韦林相比，其具有更高的活性，因此成为新的先导化合物。新颖简洁的结构为抗病毒研究提供了另一个新模板。
• Synthesis of Phenanthro[9,10-<i>b</i>]indolizidin-9-ones, Phenanthro[9,10-<i>b</i>]quinolizidin-9-one, and Related Benzolactams by Pd(OAc)₂-Catalyzed Direct Aromatic Carbonylation
  作者：Satoshi Yamashita、Nobuhito Kurono、Hisanori Senboku、Masao Tokuda、Kazuhiko Orito

  DOI：10.1002/ejoc.200801047

  日期：2009.3

  10-b]indolizidin-9-ones, phenanthro[9,10-b]quinolizidin-9-one, and related benzolactams were synthesized by benzolactam ring formation using Pd(OAc)2-catalyzed direct aromatic carbonylation. This also constitutes a formal synthesis of the representative phenanthroindolizidine and -quinolizidine alkaloids (±)-tylophorine, (±)-antofine, and (±)-cryptopleurine.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany

  菲 [9,10-b] indolizidin-9-ones、菲 [9,10-b] quinolizidin-9-one 和相关苯并内酰胺是通过使用 Pd(OAc)2 催化的直接芳香羰基化通过苯内酰胺环形成合成的。这也构成了代表性的菲吲哚里西啶和-喹唑西啶生物碱 (±)-tylophorine、(±)-antofine 和 (±)-cryptopleurine 的正式合成。 (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
• Design, Synthesis, Antiviral Activity, and Structure–Activity Relationships (SARs) of Two Types of Structurally Novel Phenanthroindo/quinolizidine Analogues
  作者：Bo Su、Fazhong Chen、Lizhong Wang、Qingmin Wang

  DOI：10.1021/jf405562r

  日期：2014.2.12

  skeletons of natural phenanthroindo/quinolizidine alkaloids on antiviral activities, two types of structurally totally novel analogues 7a, 7b, 16a, and 16b were designed, synthesized, and evaluated against tobacco mosaic virus (TMV) for the first time. Bioassay results indicated that all four of the newly designed analogues showed good to excellent antiviral activities, among which analogue 16a dispalyed

  为了研究天然菲咯菌素/喹喔啉生物碱的原始骨架变化对抗病毒活性的影响，设计，合成并评估了两种类型的结构新颖的类似物7a，7b，16a和16b，以抵抗烟草花叶病毒（TMV）。首次。生物测定结果表明，所有四个新设计的类似物均表现出良好的抗病毒活性，其中类似物16a与宁南霉素（可能是最成功的商业抗病毒药物之一）相比，其活性降低了，因此逐渐成为植物病毒的潜在抑制剂，并成为进一步优化的新途径。还讨论了进一步的构效关系，这首次证明菲咯啉吲哚和菲咯啉喹嗪的原始骨架的相同变化表现出完全不同的抗病毒活性，提供了一些有关维持高活性的优先构象的有用的原始信息。
• Total Synthesis of the Proposed Structure of Tyloindane and Its Diastereoisomer
  作者：Qingmin Wang、Bo Su、Hui Zhang

  DOI：10.1055/s-0037-1610789

  日期：2022.4

  with phenanthroindolizidine alkaloids, contains no nitrogen atom. Attracted by its unique structure and uncovered biological activity, we synthesized the proposed structure of tyloindane and its diastereoisomer. To achieve this goal, several strategies that include an aryl/alkene oxidative coupling, radical cyclization, and intramolecular Parham alkylation, were explored. The 1H NMR data of the synthesized

  有趣的是，与菲并吲哚里西啶生物碱一起分离出来的泰洛茚烷不含氮原子。受其独特的结构和未发现的生物活性所吸引，我们合成了所提出的泰洛茚烷及其非对映异构体的结构。为了实现这一目标，探索了几种策略，包括芳基/烯烃氧化偶联、自由基环化和分子内 Parham 烷基化。合成化合物的1 H NMR 数据与分离样品 (tyloindane) 的数据不匹配，表明应该重新分配 tyloindane 的结构。