Chlorogenic acid derivative capable of clearing away heat and toxic materials and preparation method thereof
A heat-clearing and detoxifying, chlorogenic acid technology, which is applied in the field of heat-clearing and detoxifying chlorogenic acid derivatives and its preparation, can solve the problems of difficult transdermal absorption, gastric mucosal irritation, unstable double bonds, etc., and achieve significant and significant inhibitory activity Inhibitory effect, good effect of inhibitory effect
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Embodiment 1
[0021] (1) Under the protection of nitrogen, dissolve 20 g of chlorogenic acid in 120 mL of methanol solution at room temperature, add 2 g of p-toluenesulfonic acid in batches, raise the temperature to 100 ° C, stir and reflux for 20 h, and TLC detects that the reaction is complete. Wash with saturated sodium bicarbonate solution and water successively, extract with ethyl acetate, combine the organic phases, dry over anhydrous sodium sulfate, and concentrate under reduced pressure to obtain Compound A;
[0022] (2) Dissolve 15.6g of Compound A in 100mL of chloroform, add 5.1g of 2-amino-3-ethylpyridine, heat up to 80°C, react for 7h, TLC detects that the reaction is complete, let stand and cool to room temperature, and vacuum the filtrate Suction filtration and drying; then transfer the dried product to a reaction container, slowly add 8.4 g of thioacetic acid dropwise at room temperature, after the dropwise addition, react for 3 hours, and when the reaction ends, add saturated...
Embodiment 2
[0025] Embodiment 2 The compound of the present invention is to the pharmacodynamics test of heat-clearing and toxic substances removing
[0026] 1. In vitro antibacterial activity experiment of medicine of the present invention
[0027] Tested strains: Staphylococcus aureus (a), Staphylococcus epidermidis (b), Candida albicans (c), Pneumococcus pneumoniae (d), Pseudomonas aeruginosa (e), beta-hemolytic streptococcus (f).
[0028] Dissolve the chlorogenic acid derivative of the present invention in absolute ethanol, dilute to 1000 μg / mL with tryptone soybean broth culture solution, continue to dilute with culture solution to make the drug concentration 256-0.25 μg / mL, and obtain the experimental solution and Qingkailing injection with a concentration range of 256-0.25 μg / mL was prepared as a positive control group (control group 1); the same method was used to prepare chlorogenic acid as a control group 2. Add a drug solution with a concentration range of 256-0.25 μg / mL and 1...
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