2-(5-formyl-2,4-dimethoxy-phenyl)-indole-1-carboxylic acid tert-butyl ester | 552845-78-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 2-(5-formyl-2,4-dimethoxy-phenyl)-indole-1-carboxylic acid tert-butyl ester
• 英文别名: 2-(5-FORMYL-2,4-DIMETHOXYPHENYL)INDOLE-1-CARBOXYLIC acid tert-butyl ester；tert-butyl 2-(5-formyl-2,4-dimethoxyphenyl)indole-1-carboxylate
• CAS: 552845-78-0
• 化学式: C₂₂H₂₃NO₅
• 分子量: 381.428
• InChiKey: YMEQXPIMQVIGDI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  66.8
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-(5-formyl-2,4-dimethoxy-phenyl)-indole-1-carboxylic acid tert-butyl ester 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 反应 96.0h， 以30%的产率得到5-(1H-indol-2-yl)-2,4-dimethoxybenzaldehyde
  参考文献：
  名称：

  [EN] PROCESS OF MAKING CHALCONE DERIVATIVES
  [FR] PROCEDE DE FABRICATION DE DERIVES DE CHALCONE

  摘要：

  公开号：

  WO2004056727A3
• 作为产物：
  描述：

  5-溴-2,4-二甲氧基苯甲醛 、 1-Boc-吲哚-2-硼酸 生成 2-(5-formyl-2,4-dimethoxy-phenyl)-indole-1-carboxylic acid tert-butyl ester
  参考文献：
  名称：

  Chalcone derivatives and their use to treat diseases

  摘要：

  本发明涉及通式或其药学上可接受的盐或酯的化合物、制药组合物及使用化合物的方法，其中取代基在申请中定义。

  公开号：

  US07094801B2

文献信息

• Sulfonamide-substituted chalcone derivatives and their use to treat diseases
  申请人：Worsencroft J. Kimberly

  公开号：US20050049236A1

  公开（公告）日：2005-03-03

  The invention relates to compounds, pharmaceutical compositions and methods of using compounds of the general formula or its pharmaceutically acceptable salt or ester, wherein the substituents are defined in the application.

  该发明涉及一般式的化合物、药物组成物和使用该化合物的方法，或其药学上可接受的盐或酯，其中取代基在申请中有定义。
• Process of making chalcone derivatives
  申请人：——

  公开号：US20040181075A1

  公开（公告）日：2004-09-16

  This invention is a novel methods of manufacturing chalcones that includes reacting a carbon-linked heteroaryl or heterocyclic substituted benzaldehyde with an acetophenone in a solvent or mixture of solvents in the presence of LiOMe. Also provided are new chalcones for the treatment of medical conditions.

  这项发明涉及一种新的合成查尔酮的方法，包括在溶剂或混合溶剂中，在LiOMe的存在下，将含有碳链的杂芳基或杂环取代苯甲醛与苯乙酮反应。同时提供了用于治疗医疗状况的新型查尔酮。
• Carboxylated, Heteroaryl-Substituted Chalcones as Inhibitors of Vascular Cell Adhesion Molecule-1 Expression for Use in Chronic Inflammatory Diseases
  作者：Charles Q. Meng、Liming Ni、Kimberly J. Worsencroft、Zhihong Ye、M. David Weingarten、Jacob E. Simpson、Jason W. Skudlarek、Elaine M. Marino、Ki-Ling Suen、Charles Kunsch、Amy Souder、Randy B. Howard、Cynthia L. Sundell、Martin A. Wasserman、James A. Sikorski

  DOI：10.1021/jm0614230

  日期：2007.3.1

  Starting from a simple chalcone template, structure-activity relationship (SAR) studies led to a series of carboxylated, heteroaryl-substituted chalcone derivatives as novel, potent inhibitors of vascular cell adhesion molecule-1 (VCAM-1) expression. Correlations between lipophilicity determined by calculated logP values and inhibitory efficacy were observed among structurally similar compounds of the series. Various substituents were found to be tolerated at several positions of the chalcone backbone as long as the compounds fell into the right range of lipophilicity. The chalcone alpha,beta-unsaturated ketone moiety seemed to be the pharmacophore required for inhibition of VCAM-1 expression. Compound 19 showed significant antiinflammatory effects in a mouse model of allergic inflammation, indicating that this series of compounds might have therapeutic value for human asthma and other inflammatory disorders.
• US7094801B2
  申请人：——

  公开号：US7094801B2

  公开（公告）日：2006-08-22
• US7173129B2
  申请人：——

  公开号：US7173129B2

  公开（公告）日：2007-02-06