methyl (E)-3-(4-oxo-4H-chromen-3-yl)acrylate | 115237-36-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: methyl (E)-3-(4-oxo-4H-chromen-3-yl)acrylate
• 英文别名: methyl (E)-3-(4-oxochromen-3-yl)prop-2-enoate
• CAS: 115237-36-0
• 化学式: C₁₃H₁₀O₄
• 分子量: 230.22
• InChiKey: XUWOEDIFNCTUHW-VOTSOKGWSA-N

物化性质

• 熔点：
  138-139 °C
• 沸点：
  347.3±42.0 °C(Predicted)
• 密度：
  1.346±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  三乙胺 、 methyl (E)-3-(4-oxo-4H-chromen-3-yl)acrylate 在 rhodamine 6G 作用下， 以 氯仿 为溶剂， 以83 %的产率得到Methyl 3-(2-hydroxybenzoyl)benzoate
  参考文献：
  名称：

  通过双惰性 C(sp3)–H 键激活可见光促进二烯和烷基胺的 [4π + 2σ] 成环

  摘要：

  在此，可见光促进的二烯和烷基胺的[4π + 2σ]成环是通过烷基胺的双C(sp 3 )–H键功能化实现的。难以捉摸的烯胺前体在温和的条件下通过光氧化还原催化生成，被二烯有效地成环，并同时用两个脂肪族 C(sp 3 )–H 键进行官能化，从而高效合成新的芳环。芳环结构可直接以高产率（高达 90%）获得 2-羟基二苯甲酮衍生物。该[4π+2σ]环化反应反应条件温和，反应效率高，具有广泛的官能团耐受性，该合成方案已可用于天然产物和商业药物的后期转化。

  DOI：

  10.1021/acs.orglett.4c01470
• 作为产物：
  描述：

  色酮-3-甲醛 在 盐酸 作用下， 以 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 16.33h， 生成 methyl (E)-3-(4-oxo-4H-chromen-3-yl)acrylate
  参考文献：
  名称：

  杂二烯环加成反应：一些取代的吡喃并[4,3- b ] [1]苯并吡喃的制备和转化

  摘要：

  4-氧代-4 H -1-苯并吡喃在C-3处具有甲酰基，乙酰基或羧基取代基的异二烯环加成反应会生成3-烷氧基-或3,3-二烷氧基-4， 4a-二氢吡喃并[4,3- b ] [1]苯并吡喃-10-酮，在某些情况下，能够在多种条件下进行多种选择性转化，包括酸诱导的差向异构和/或逆环加成，还原，水解和醇解非常温和的条件。

  DOI：

  10.1016/s0040-4020(01)85668-4

文献信息

• The Domino Chromone Annulation and a Transient Halogenation-Mediated C–H Alkenylation toward 3-Vinyl Chromones
  作者：Leiqing Fu、Zhongrong Xu、Jie-Ping Wan、Yunyun Liu

  DOI：10.1021/acs.orglett.0c03548

  日期：2020.12.18

  Reported in this paper is a step economical method toward the general synthesis of 3-vinyl chromones via the reactions between readily available o-hydroxyphenyl enaminones and various alkenes. The domino C–H alkenylation and chromone annulation of the enaminones are involved, which enables the synthesis of 3-vinyl chromone products using both terminal and internal alkenes via a key process of transient C–H

  本文报道的是一种通过经济实用的步骤逐步实现3-乙烯基色酮的合成的方法，该方法是通过容易获得的邻-羟基苯基烯胺酮与各种烯烃之间的反应进行的。涉及烯胺酮的多米诺骨化CHH烯基化和色酮环化，这可以通过瞬态CHH卤化的关键过程使用末端烯烃和内部烯烃合成3-乙烯基色酮产物。
• Synthesis of Conjugated Dienes via a Biomimetic Aerobic Oxidative Coupling of Two C_vinylH Bonds
  作者：Nicolas Gigant、Jan-E. Bäckvall

  DOI：10.1002/chem.201301771

  日期：2013.8.12

  A time to dienes: A highly efficient and general method has been developed to prepare conjugated dienes through a biomimetic approach. This aerobic oxidative coupling, involving two CvinylH bonds, proceeds under low Pd catalyst loading and employs catalytic amounts of p‐benzoquinone and iron phthalocyanine as electron‐transfer mediators (ETMs) under ambient oxygen pressure (see scheme).

  二烯的时间：已经开发出一种高效且通用的方法来通过仿生方法制备共轭二烯。这种好氧氧化偶合，涉及两个C乙烯基H键，在低Pd催化剂负载下进行，并在环境氧压下采用催化量的对苯二醌和酞菁铁作为电子传递介质（ETM）（请参见方案）。
• Substituted 4H-1-benzopyran-4-ones (chromones): synthesis via palladium-catalysed coupling of their halogeno derivatives with alkenes
  作者：Stephen G. Davies、Bryan E. Mobbs、Christopher J. Goodwin

  DOI：10.1039/p19870002597

  日期：——

  into the carbon–halogen bond. The resultant species undergo coupling with alkenes leading to vinylated chromones. Vinylation occurs regiospecifically at the original site of bromination and therefore provides a method for the clean introduction of substituents into the chromone ring system. An anomalous reaction of a dibrominated chromone leading to a ring-opened product is described.

  溴色酮的活化是通过将Pd 0插入碳-卤素键来实现的。所得的物质与烯烃偶联，产生乙烯基化的色酮。乙烯基化区域特异性地在溴化的原始位置发生，因此提供了将取代基干净地引入色酮环系统的方法。描述了二溴苯甲酮的异常反应导致开环产物。
• Palladium(II)-Catalyzed Direct Intermolecular Alkenylation of Chromones
  作者：Donghee Kim、Sungwoo Hong

  DOI：10.1021/ol2018278

  日期：2011.8.19

  A new efficient method for the direct alkenylation of chromones via a palladium(II)-catalyzed C-H functionalization reaction was developed. The use of pivalic acid with Cu(OAc)(3)/Ag2CO3 provided superior reactivity in the cross-coupling of chromones with alkene partners. This approach represents a significant advance over the existing two-step method and afforded various 3-vinylchromone derivatives, which are privileged structures in many biologically active compounds and versatile synthetic building blocks.
• Synthesis, Antiproliferative, and c-Src Kinase Inhibitory Activities of 4-Oxo-4<i>H</i>-1-benzopyran Derivatives
  作者：Karam Chand、Rakesh K Tiwari、Sumit Kumar、Amir Nasrolahi Shirazi、Sweta Sharma、Erik V Van der Eycken、Virinder S Parmar、Keykavous Parang、Sunil K Sharma

  DOI：10.1002/jhet.2106

  日期：2015.3

  A new class of 4‐oxo‐4H‐1‐benzopyran derivatives were synthesized and their antiproliferative activity examined against a panel of three human cancer cell lines, that is, breast carcinoma (MDA‐MB‐468), ovarian adenocarcinoma (SK‐OV‐3), and colorectal adenocarcinoma (HT‐29). Two compounds, that is, 3‐hexyl‐7,8‐dihydroxy‐4‐oxo‐4H‐1‐benzopyran and (E)‐ethyl 3‐(7‐methoxy‐4‐oxo‐4H‐1‐benzopyran‐3‐yl)acrylate were found to be potent against all three cancer cell lines studied at 50 μM concentration. Also, the inhibitory potency of the compounds was evaluated against active Src kinase. A few of these compounds exhibited modest Src kinase inhibitory activity (IC50 = 52–57 μM). Structure‐activity relationship studies with respect to the nature and position of substituents on the lead compounds could be further exploited for the design and development of more potent antiproliferative agents and/or Src kinase inhibitors.