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A kind of preparation method of roquinex

A technology of oxoquinoline and dihydrogen, which is applied in the preparation field of preparing a roquimec, can solve the problem of stability and mechanical strength, which have not been reported further, and that methanol cannot be completely separated from the system, affecting product content and yield. and other problems, to achieve the effect of shortening the reaction time, reducing the amount of solvent used, and improving the yield and purity

Active Publication Date: 2020-11-13
湖南速博生物技术有限公司
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  • Abstract
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  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] 1. Since the main reaction is an equilibrium reaction, the methanol produced by the reaction cannot be completely separated from the system, which affects the yield
[0009] 2. Due to the unavoidable existence of trace amounts of water in the system, the raw materials and products are hydrolyzed, which affects the product content and yield
[0010] 3. Separate the methanol and water in the solvent from the system by distillation. Although the method of adding fresh solvent at the same time can be used to promote the reaction balance to move to the right to a certain extent, the operation is cumbersome and the solvent loss is large. After recovery The solvent also needs to separate the methanol separately
[0011] 4. Long reaction time
[0013] There are also reports in the literature that permeable membranes are used for the separation of methanol and other solvents, such as literature (Methanolremoval from organic mixtures by pervaporation using polypyrrole membranes, Ming Zhou et al, Journal of Membrane Science, No. 117, No. 1-2, No. 303 -309 pages, published on August 21, 1996), using a polypyrrole membrane to separate methanol from other solvents, the membrane is kept in contact with the feed liquid during the separation process, the liquid mixture swells the membrane, and the feed liquid is circulated in the pool , and then apply a vacuum on the other side of the membrane to make methanol permeate through the membrane. The membrane is separated by direct contact with the liquid. Compared with the gas permeable membrane and the solvent gas contact, the membrane is not in contact with the high temperature solvent gas, and the separation efficiency Low, the film is an organic film, its thermal stability may be poor at high temperature, and its stability and mechanical strength have not been further reported

Method used

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  • A kind of preparation method of roquinex
  • A kind of preparation method of roquinex
  • A kind of preparation method of roquinex

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] 30.0 g 1,2-dihydro-4-hydroxy-1-methyl-2-oxoquinoline-3-carboxylic acid methyl ester (0.13 mol), 18.1 g N-methylaniline (0.17 mol) and 120 g Add n-heptane and 1.2 g of anhydrous calcium chloride into a 250 mL three-necked flask, connect the flask to the inlet of a type A molecular sieve pervaporation inorganic membrane device, stir and heat to reflux, and reflux for 3.5 h. During the reaction, the methanol in the organic vapor and The water mixture passes through the A-type molecular sieve to infiltrate and vaporize the inorganic membrane tube to separate the system, and the solvent is refluxed back to the kettle for reaction. At the end of the reaction, a total of 5.1 g of methanol and water were collected. The reaction solution was filtered at 70°C, the filter cake was used as a catalyst, the filtrate was cooled and crystallized and filtered, and the filter cake was dried to obtain 39.2 g of white solid with a content of 99.6% (external standard of liquid chromatograph...

Embodiment 2

[0034] 30.0 g 1,2-dihydro-4-hydroxy-1-methyl-2-oxoquinoline-3-carboxylic acid methyl ester (0.13 mol), 18.1 g N-methylaniline (0.17 mol) and 180 g Cyclohexane and 1.8 g of anhydrous calcium chloride were added to a 250 mL three-necked flask, and the flask was connected to the inlet of a type A molecular sieve pervaporation inorganic membrane device, stirred and heated to reflux, and refluxed for 2.5 h. During the reaction, the methanol in the organic vapor and The water mixture passes through the A-type molecular sieve to infiltrate and vaporize the inorganic membrane tube to separate the system, and the solvent is refluxed back to the kettle for reaction. At the end of the reaction, a total of 5.1 g of methanol and water were collected. The reaction solution was filtered at 60°C, the filter cake was used as a catalyst (for the next batch of reactions), the filtrate was cooled, crystallized and filtered, and the filter cake was dried to obtain 39.3 g of white solid, with a con...

Embodiment 3

[0036] 30.0 g 1,2-dihydro-4-hydroxy-1-methyl-2-oxoquinoline-3-carboxylic acid methyl ester (0.13 mol), 14.9 g N-methylaniline (0.14 mol) and 150 g Add n-heptane and 1.5 g of anhydrous calcium chloride into a 250 mL three-neck flask, connect the flask to the inlet of a type A molecular sieve pervaporation inorganic membrane device, stir and heat to reflux, and reflux for 3 h. During the reaction, methanol and The water mixture passes through the A-type molecular sieve to infiltrate and vaporize the inorganic membrane tube to separate the system, and the solvent is refluxed back to the kettle for reaction. After the reaction, a total of 5.2 g of methanol and water were collected. The reaction solution was filtered at 65°C, the filter cake was used as a catalyst, the filtrate was cooled and crystallized and filtered, and the filter cake was dried to obtain 39.3 g of white solid with a content of 99.5% (LC external standard) and a yield of 98.5% (with 1,2-dihydro -4-Hydroxy-1-met...

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Abstract

A preparation method of roquinimex comprises the following steps: carrying out a reflux reaction on 1, 2-dihydro-4-hydroxy-1-methyl-2-oxoquinoline-3-methyl formate shown as a formula II, N-methylaniline shown as a formula III and a catalyst calcium chloride in a solvent, removing methanol generated by reaction and trace water in the system by adopting an A-type molecular sieve pervaporation inorganic membrane, ending the reaction, filtering a reaction solution at 60-70 DEG C after the reaction is finished, cooling and crystallizing a filtrate, and carrying out filtering and drying to obtain the N-methyl-N-phenyl-1, 2-dihydro-4-hydroxy-1-methyl-2-oxoquinoline-3-formamide (roquinimex) shown in a formula I. The yield reaches 98.5%, and the product content reaches 99.7% (liquid spectrum external standard). The preparation method has the advantages of simple process, no need of distillation, high product purity and yield and the like.

Description

technical field [0001] The invention relates to a preparation method of roquinex. More specifically, the present invention relates to an improved and simplified process for the preparation of roquinex. Background technique [0002] Roquinex (Chinese name: N-methyl-N-phenyl-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxamide) was found to be An effective immunomodulator, it has therapeutic effects on various autoimmune diseases in animal experiments. Due to its pharmacological properties of high activity and low side effects, this compound is considered valuable in the treatment of diseases caused by pathological inflammation and autoimmune diseases, as well as various malignant tumors. N-methyl-N-phenyl-1,2-dihydro-4-hydroxy-1-methyl-2-oxoquinoline-3- Formamide. Said patent discloses four preparation methods. Compounds are prepared by reacting carboxylic acids with amines in the presence of pyridine or quinoline as an inert solvent. US5912349 discloses an impr...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07D215/56
CPCC07D215/56
Inventor 杨紫冬胡志彬
Owner 湖南速博生物技术有限公司
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