3-(3',4'-dimethoxyphenyl)-8-methoxycoumarin | 54208-22-9

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 异黄酮类化合物
• 英文名称: 3-(3',4'-dimethoxyphenyl)-8-methoxycoumarin
• 英文别名: 3-(3,4-dimethoxyphenyl)-8-methoxy-2H-chromen-2-one；3-(3,4-dimethoxy-phenyl)-8-methoxy-chromen-2-one；3-(3,4-dimethoxyphenyl)-8-methoxychromen-2-one
• CAS: 54208-22-9
• 化学式: C₁₈H₁₆O₅
• mdl: MFCD06644425
• 分子量: 312.322
• InChiKey: PLZMPTVQPGFVSD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  54
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-(3',4'-dimethoxyphenyl)-8-methoxycoumarin 在 1,10-菲罗啉 、 copper(l) chloride 、 sodium hydroxide 作用下， 以 二甲基亚砜 为溶剂， 反应 24.0h， 以36%的产率得到2-(3,4-dimethoxyphenyl)-7-methoxybenzofuran
  参考文献：
  名称：

  Copper-catalyzed decarboxylative intramolecular C–O coupling: synthesis of 2-arylbenzofuran from 3-arylcoumarin

  摘要：

  建立了一种铜催化的脱羧分子内 CâO 偶联反应。在氯化铜/1,10-菲罗啉存在的有氧条件下，以 3-芳基香豆素为原料一锅制备了多种 2-芳基苯并呋喃，收率从 26% 到 84%不等。

  DOI：

  10.1039/c3ra46414h
• 作为产物：
  描述：

  3,4-二甲氧基苯乙酸 、 邻香草醛 在 乙酸酐 、 三乙胺 作用下， 反应 8.0h， 以65%的产率得到3-(3',4'-dimethoxyphenyl)-8-methoxycoumarin
  参考文献：
  名称：

  3-Arylcoumarins: Synthesis and potent anti-inflammatory activity

  摘要：

  Chronic inflammation is the persistent and excessive immune response and can lead to a variety of diseases. Aiming to discover new compounds with anti-inflammatory activity, we report herein the synthesis and biological evaluation of 3-arylcoumarins. Thirty five 3-arylcoumarins were prepared through Perkin condensation and further acid-promoted hydrolysis if necessary. In lipopolysaccharide-activated mouse macrophage RAW264.7 cells, 6,8-dichloro-3-(2-methoxyphenyl) coumarin (16) and 6-bromo-8-methoxy-3-(3-methoxyphenyl) coumarin (25) exhibited nitric oxide production inhibitory activity with the IC50 values of 8.5 mu M and 6.9 mu M, respectively, providing a pharmacological potential as anti-inflammatory agents. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2014.10.033

文献信息

• A one-pot domino C–H, C–C activation in coumarins: a fast track to 2,3-diaryl benzo[<i>b</i>]furans
  作者：Mehdi Khoobi、Fatemeh Molaverdi、Farnaz Jafarpour、Masoumeh Abbasnia、Maciej Kubicki、Abbas Shafiee

  DOI：10.1039/c5cc01427a

  日期：——

  An approach to synthesize 2,3-diaryl benzo[b]furans using coumarins and aryl bromides is developed.

  使用香豆素和芳基溴化物合成2,3-二芳基苯并呋喃的方法已经开发。
• 2-Phenylbenzo[ b ]furans: Synthesis and promoting activity on estrogen biosynthesis
  作者：Wenchen Pu、Yun Yuan、Danfeng Lu、Xin Wang、Hanwei Liu、Chun Wang、Fei Wang、Guolin Zhang

  DOI：10.1016/j.bmcl.2016.10.013

  日期：2016.11

  2-phenylbenzo[b]furan glycosides could promote estrogen biosynthesis. To find high active 2-phenylbenzo[b]furans, fifty-four 2-phenylbenzo[b]furans were prepared via four strategies according to corresponding substrate scopes. Biological evaluation in HEK293A cells showed that some compounds exhibited promotive activity on estrogen biosynthesis. 2-(4-Chlorophenyl)-7-methoxybenzo[b]furan possessed the

  雌激素的生物合成对人类的许多生理过程至关重要。雌激素水平异常与多种疾病密切相关，包括乳腺癌和骨质疏松症。以前我们发现2-苯基苯并[b]呋喃糖苷可以促进雌激素的生物合成。为了找到高活性的2-苯基苯并[b]呋喃，根据相应的底物范围，通过四种策略制备了五十四种2-苯基苯并[b]呋喃。HEK293A细胞的生物学评估表明，某些化合物对雌激素的生物合成具有促进作用。2-（4-氯苯基）-7-甲氧基苯并[b]呋喃具有最高的活性，EC50值为14.68μM。此外，这些化合物不会影响HEK292A细胞中的芳香化酶表达，
• Synthesis and Evaluation of Coumarin–Resveratrol Hybrids as 15-Lipoxygenaze Inhibitors
  作者：Samira Rahmani-Nezhad、Leila Khosravani、Mina Saeedi、Kouros Divsalar、Loghman Firoozpour、Yaghoub Pourshojaei、Yaghoub Sarrafi、Hamid Nadri、Alireza Moradi、Mohammad Mahdavi、Abbas Shafiee、Alireza Foroumadi

  DOI：10.1080/00397911.2014.979947

  日期：2015.3.19

  A series of coumarin-resveratrol hybrids, 3-arylcoumarin derivatives 3a-u, were synthesized through the intermolecular condensation reaction of various salicylaldehydes and phenylacetic acids in the presence of 1,4-diazabicyclo[2.2.2]octane under solvent-free conditions. All the synthesized compounds were screened for their inhibitory potency against soybean 15-lipoxygenase. Among them, three compounds (3c, 3j, and 3q) showed good enzyme-inhibitory activities.
• (Z)-2-Acetoxy-3,3',4'-trimethoxystilbene
  作者：S. Li、K. Lundquist、R. Stomberg

  DOI：10.1107/s0108270196011079

  日期：1996.12.15

  The crystal structure determination demonstrates unambiguously that the title compound, 2-[(Z)-3,4-dimethoxyphenylethenyl]-6-methoxypheenyl acetate, C19H20O5, has the Z configuration. The title compound was prepared by decarboxylation of (E)-3-(2-acetoxy-3 -methoxyphenyl)-2-(3,4-dimethoxyphenyl)propenoic acid; this compound was in turn obtained by condensation of 2-acetoxy-3-methoxybenzaldehyde with (3,4-dimethoxyphenyl)acetic acid. H-1 NMR data for the titie compound and the isomeric (E)-2-acetoxy-3,3',4'-trimethoxystilbene are reported.