Biguanide derivative for preventing and treating infarction diseases and application thereof

A biguanide derivative and infarction technology, which is applied in blood diseases, extracellular fluid diseases, cardiovascular system diseases, etc., can solve the problems of lack of mode of action and mechanism, and ineffective effects, so as to reduce production costs and achieve high economic efficiency , simple structure and synthetic process

Active Publication Date: 2019-06-25
WEST CHINA HOSPITAL SICHUAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Evidence-based medicine has confirmed that in the treatment of diabetes, metformin can not only reduce sugar and improve blood lipid metabolism, but also reduce the morbidity and mortality of cardiovascular diseases, but there is still a lack of reports on its specif

Method used

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  • Biguanide derivative for preventing and treating infarction diseases and application thereof
  • Biguanide derivative for preventing and treating infarction diseases and application thereof
  • Biguanide derivative for preventing and treating infarction diseases and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] In this example, guanidinated metformin derivatives were synthesized, specifically including compounds 1-4.

[0024] 1. Synthesis of compound 1: N-(4-dimethylaminobenzylidene) metformin

[0025] Take 1.29g (10.0mmol) of metformin, 1.49g (10.0mmol) of 4-dimethylaminobenzaldehyde, 150mL of ethanol, and 2mL of acetic acid in a 250mL flask, and carry out a stirring reaction at 78°C. The progress of the reaction was detected by TCL, and the reaction was basically complete after about 6 hours. Add sodium bicarbonate to adjust the pH value to neutral to quench the reaction, then spin dry under reduced pressure to obtain a crude product, and then use petroleum ether: ethyl acetate = 2:1 (v / v) as an eluent to pass through a silica gel column, 2.3 g of compound 1 was obtained as a white powder with a yield of 90%. R f is 0.6 (dichloromethane:methanol:glacial acetic acid=9:1:0.025).

[0026] Compound 1 was detected by proton NMR spectrum, carbon NMR spectrum and mass spectrome...

Embodiment 2

[0045] In this example, sulfonamide metformin derivatives were synthesized, specifically including compounds 11-20.

[0046] 1. Synthesis of compound 11: N-(2,2,2-trifluoroethylsulfonyl) metformin

[0047] Take 1.29g (10.0mmol) metformin, 1.82g (10.0mmol) 2,2,2-trifluoroethylsulfonyl chloride, 300mL anhydrous acetone, 0.056g (1mmol) potassium hydroxide in a 500mL flask, and stir overnight at room temperature. Use TCL to detect the reaction process. When there is no obvious change in the reaction product, add dilute hydrochloric acid to adjust the pH value to neutral to quench the reaction, then spin dry under reduced pressure to obtain the crude product, and then use petroleum ether:ethyl acetate=2:1 (v / v) was used as an eluent to pass through a silica gel column to obtain 2.5 g of compound 11 as a white powder, with a yield of 90%. R f is 0.7 (dichloromethane:methanol:glacial acetic acid=9:1:0.025).

[0048] Compound 11 was detected by H NMR spectrum, C NMR spectrum and ma...

Embodiment 3

[0097] In this example, amidated metformin derivatives were synthesized, specifically including compounds 5-10.

[0098] 1. Synthesis of compound 5: N-(2,2,2-trifluoroacetyl) metformin

[0099] Take 1.29g (10.0mmol) metformin, 2.10g (10.0mmol) trifluoroacetic anhydride, 300mL anhydrous acetone, 0.056g (1mmol) potassium hydroxide in a 500mL flask, and stir overnight at room temperature. Use TCL to detect the reaction process. When there is no obvious change in the reaction product, add dilute hydrochloric acid to adjust the pH value to neutral to quench the reaction, then spin dry under reduced pressure to obtain the crude product, and then use petroleum ether:ethyl acetate=2:1 (v / v) was used as an eluent to pass through a silica gel column to obtain 2.0 g of white powder compound 5 with a yield of 89%. R f is 0.7 (dichloromethane:methanol:glacial acetic acid=9:1:0.025).

[0100] Compound 5 was detected by proton nuclear magnetic spectrum, carbon nuclear magnetic spectrum an...

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Abstract

The invention provides a biguanide derivative for preventing and treating infarction diseases and application of the biguanide derivative in preparation of a medicine for preventing and treating the infarction diseases. The biguanide derivative has an antiplatelet effect, has an obvious inhibition effect on formation of pulmonary embolism, arterial thrombosis and venous thrombosis, can effectivelyreduce cerebral infarction area and cardiac infarction area, and has an obvious improvement effect on cerebral infarction and myocardial infarction. The effect of the derivative is obviously better than that of a positive control medicine, aspirin. The biguanide derivative can also reduce gastrointestinal side effects and bleeding risks commonly existing in existing clinical antithrombotic drugs.

Description

technical field [0001] The invention belongs to the field of medicines, and relates to biguanide derivatives for preventing and treating infarction diseases, and the application of the biguanide derivatives in preparing medicines for preventing and treating infarction diseases. Background technique [0002] Nowadays, with the changes in people's lifestyle and diet structure, vascular diseases based on thrombosis have become the biggest threat to human life. At present, there are about 415 million diabetic patients in the world, and about 5 million people die from diabetes and its complications every year, and about 3.2 million diabetic patients die from its thrombotic complications. At present, antithrombotic drugs used clinically generally have increasing tolerance and side effects, among which bleeding risk and gastrointestinal side effects are the most common and serious side effects. For example, aspirin, the most widely used antithrombotic drug in clinical practice, ha...

Claims

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Application Information

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IPC IPC(8): C07C279/26C07C311/09C07C311/14C07C311/03A61P7/02A61P9/10
Inventor 黄文
Owner WEST CHINA HOSPITAL SICHUAN UNIV
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