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Novel preparation process of linagliptin

A one-pot, reaction technology, applied in metabolic diseases, organic chemistry, drug combination, etc., can solve the problems of three wastes, high cost, and few varieties

Inactive Publication Date: 2021-01-12
山东永丞制药有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0014] 1) The cost of starting materials and reagents; 2) The cost of equipment, safety, and environmental protection; 3) The cost of three wastes treatment; 4) Labor cost
[0015] After a comprehensive analysis, 2-4 are the key points of cost, and one of the keys is the problem of the three wastes: the generation of the three wastes directly leads to the treatment cost of the three wastes, the cost of safety and environmental protection, and the cost of labor
In the traditional synthesis method of linagliptin, potassium carbonate and the like need to be added as an acid-binding agent during the reaction process, and acid-base neutralization produces a large amount of salt, and the waste water has obvious defects;
[0017] ②Microchannel reaction: Among the emerging synthesis methods in recent years, microchannel reaction has undergone a lot of publicity and reports, and it is still in the preliminary stage in China, and it is still immature, and there are many areas that need to be improved. There are still fewer varieties produced by channel reaction, and the cost is very high, which does not match the current demand for centralized procurement;
[0019] In the current relevant literature reports, there is no report on the three-step reaction "one-pot stew" preparation method of linagliptin

Method used

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  • Novel preparation process of linagliptin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044]Step 1: Preparation of 8-bromo-7-(2-butyne)-3-methyl-1H-purine-2,6(3,7-dihydro)-dione

[0045] 100 g 8-bromo-3-methylxanthine, 57 g 1-bromo-2-butyne (1.05 eq), 900 ml DMF, 63.3 g DIPEA (1.2 eq) were added to the reaction flask. Stir at room temperature, TLC detection, complete reaction in 18 hours, and an off-white solid is obtained.

[0046] Step 2: Preparation of 8-bromo-7-(2-butyn-1-yl)-3,7-dihydro-3-methyl-1-[(4-methyl-2-quinazolinyl)methanol base]-1H-purine-2,6-dione

[0047] Add 82.5 g of 2-chloromethyl-4-methylquinazole (1.05 eq) to the reaction flask of the first step above, stir at 60-70° C., detect by TLC, the reaction is complete in 13 hours, and it is directly used in the next step.

[0048] Step 3: Preparation of Linagliptin

[0049] Add 74.2g of (R)-3-aminopiperidine dihydrochloride (1.05eq) to the reaction flask of the second step above, continue to stir at 60-70°C, detect by TLC, and the reaction is complete in 7 hours. Evaporate the solvent under red...

Embodiment 2

[0051] Different from Example 1: the catalyst triethylamine is 49.6g (1.2 equivalents), the total yield of the three-step reaction is 76.3%, and the HPLC purity is 99.68%.

Embodiment 3

[0053] Different from Example 1: the amount of DIPEA is 68.6g (1.3 equivalents), the total yield of the three-step reaction is 77.9%, and the HPLC purity is 99.72%.

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Abstract

The invention discloses a novel preparation process of linagliptin. 8-bromo-3-methyl xanthine (SM1) is used as an initial raw material, DMF is used as a solvent and reacts with 1-bromo-2-butyne (SM2)under the alkaline condition to obtain an intermediate I, then the intermediate I reacts with 2-chloromethyl-4-methyl quinazol (SM3) under the solvent system to obtain an intermediate II, the intermediate II and (R) 3-aminopiperidine dihydrochloride (SM4) are subjected to a substitution reaction, and finally anti-type 2 diabetes drug linagliptin (I) is prepared. By adopting a one-pot method, the method has the advantages that the raw material cost is low, the yield is high, the post-treatment operation of each step of chemical reaction in multi-step reaction is reduced, the production period is greatly shortened, few impurities are generated in the reaction, the product quality is high, the use amount of chemical reagents is relatively reduced, and the method is relatively green and environment-friendly, and is beneficial to industrial production.

Description

technical field [0001] The invention belongs to the technical field of medicine synthesis, and in particular relates to a new preparation process of linagliptin, a medicine for treating type 2 diabetes. Background technique [0002] According to the research statistics of the World Health Organization, there are more than 400 million people with diabetes worldwide, most of whom are type 2 diabetes. According to the results of the "China Chronic Disease Monitoring and Diabetes Special Survey" released by the China Health Education Center, in 2012, there were about 97 million adult diabetic patients nationwide, of which type 2 diabetes accounted for 90% of the total patients. It is estimated that by 2025 or 2030, the number of people with diabetes in developed countries like Europe and the United States will increase by 130%. According to the British Medical Journal report on April 28 this year, the latest epidemiological data on diabetes were released, and the total number o...

Claims

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Application Information

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IPC IPC(8): C07D473/04A61P3/10
CPCC07D473/04A61P3/10
Inventor 陈胜
Owner 山东永丞制药有限公司
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