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Evodiamine compounds, preparation method thereof and application thereof

A technology of evodiamine and its compounds, applied in the field of evodiamine compounds and their medicinal salts, can solve the problems of high toxicity and poor water solubility, and achieve good anti-tumor activity

Inactive Publication Date: 2012-01-11
SECOND MILITARY MEDICAL UNIV OF THE PEOPLES LIBERATION ARMY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the lactone structure necessary for the activity of this type of compound is hydrolyzed too quickly in the human body into an inactive carboxylate, and has poor water solubility and high toxicity

Method used

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  • Evodiamine compounds, preparation method thereof and application thereof
  • Evodiamine compounds, preparation method thereof and application thereof
  • Evodiamine compounds, preparation method thereof and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0060] Embodiment 1: the synthesis of 1-methyl evodiamine

[0061] A. Preparation of N-formyltryptamine

[0062] In a 50ml three-necked bottle, add 8g (50mmol) of tryptamine and 25g of ethyl formate, and reflux at 80°C for 12 hours. After the reaction, the solvent is evaporated to dryness to obtain a brown oil, which is left at room temperature for 2-3 days, and crystals slowly appear. Suction filtration obtained 7.3 g of the product with a yield of 87.1%.

[0063] B. Preparation of 3,4-dihydro-β-carboline

[0064] In a 100ml three-neck flask, add 50ml of dichloromethane, under stirring conditions, add 5g (26mmol) N-formyl tryptamine, cool to about 5°C in an ice-water bath, then slowly add 12.5ml of phosphorus oxychloride, ice React in the bath for 2 hours, and then react at room temperature for 2 hours. After the reaction, dichloromethane and unreacted phosphorus oxychloride were recovered by distillation under reduced pressure, and the residual solid was extracted three ti...

Embodiment 2

[0071] Example 2: Synthesis of 4-fluoroevodiamine

[0072] According to the method of Example 1, in step C, 6-fluoroanthranilic acid is used instead of 3-methylanthranilic acid to obtain 5-fluoropyridine red acid anhydride, and in step D, 5-fluoropyridine red acid anhydride is used instead of 8- Methylidine red anhydride to get N-methyl-5-fluoropyridine red anhydride, replace N-methyl-8-methylpyridine red anhydride with N-methyl-5-fluoropyridine red anhydride in step E to get gray powder 0.47g of 4-fluoroevodiamine, the total yield is 36.5%.

Embodiment 3

[0073] Embodiment 3: the synthesis of 4-chloroevodiamine

[0074] According to the method of Example 1, in step C, 3-methylanthranilic acid is replaced with 6-chloroanthranilic acid to obtain 5-chloropyridine red acid anhydride, and in step D, 5-chlororidine red acid anhydride is used to replace 8- Methylidine red anhydride to get N-methyl-5-chloropyridine red anhydride, in step E replace N-methyl-8-methylpyridine red anhydride with N-methyl-5-chlororidine red anhydride to get gray powder 0.64g of 4-chloroevodiamine, with a total yield of 47.5%.

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PUM

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Abstract

The invention relates to the technical field of medicines. The content of DNA topoisomerase I (TopoI) in tumor cells is substantially higher the content of the TopoI in normal tissues, and an inhibitor of the TopoI is listed as one of six types of antitumor drugs which are primarily researched by an American NCI (National Cancer Institute). The invention aims to obtain evodiamine derivatives withstrong antitumor activities by modifying the structure of evodiamine. The evodiamine structure of the evodiamine compounds is represented by general formula (I) in the specification. The invention also provides an application of the evodiamine compounds and medicinal salts thereof in preparing topoisomerase inhibitors and antitumor drugs.

Description

technical field [0001] The invention relates to the technical field of medicine, in particular to evodiamine compounds and their medicinal salts, their preparation methods and applications. Background technique [0002] DNA topoisomerase I (topoisomerase I, TopoI) is an essential enzyme for cell DNA replication, transcription, recombination and repair, and the content of TopoI in tumor cells, especially colon cancer, cervical cancer, ovarian cancer, etc. is much higher than that in normal tissues , so this type of drug has high selectivity for tumor cells. Inhibitors of this enzyme have been listed as one of the six major categories of anti-tumor drugs by the US NCI. [0003] Camptothecin is a classic topoisomerase I inhibitor. At present, three camptothecin compounds have entered clinical use, namely Irinotecan, Topotecan and Belotecan. . However, the lactone structure necessary for the activity of this type of compound is hydrolyzed too quickly in the human body into an...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D471/14A61K31/519A61P35/00
Inventor 盛春泉张万年董国强王胜正缪震元姚建忠张永强祝令建庄春林
Owner SECOND MILITARY MEDICAL UNIV OF THE PEOPLES LIBERATION ARMY
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