Human breast cancer cell inhibitor and preparation method thereof
A technology of human breast cancer cells and inhibitors, which is applied in the direction of pharmaceutical formulations, medical preparations containing active ingredients, drug combinations, etc., can solve problems such as prone to complications, serious physical damage, and low immunity, and the method is simple Easy to operate, good stability, and growth-inhibiting effect
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Embodiment 1
[0050] One, preparation method of the present invention:
[0051] (1) The preparation method of 2,2'-bisbenzimidazole is as follows: Weigh 1.42 grams (10 mmol) of ammonium oxalate and 2.16 grams of o-phenylenediamine (20 mmol) as reactants, add 15 mL of glycerol, and mix well Finally, put it into the microwave rapid reaction system and react for 10 minutes at a power of 200w and a temperature of 250°C; then react at a power of 300w and a temperature of 165°C for 11 minutes. Filter and wash with distilled water two to three times to obtain the crude product. Recrystallize the crude product with 100mL of ethylene glycol, filter it with suction, put the product in a drying oven at 80°C, and bake it for 2 hours to obtain a yellow powder compound that is 2,2'-bisbenzimidazole; it was analyzed by infrared spectroscopy Determination, the obtained infrared spectrum is as follows figure 2 shown.
[0052] (1) Zn(NO 3 ) 2 ·6H 2 O (0.5 mmol), 2,2'-bisbenzimidazole (0.25 mmol), 5-hy...
Embodiment 2
[0073] One, preparation method of the present invention:
[0074] (1) The preparation method of 2,2'-bisbenzimidazole is as follows: Weigh 2.84 g (20 mmol) of ammonium oxalate and 4.32 g of o-phenylenediamine (40 mmol) as reactants, add 20 mL of glycerol, and mix well Finally, put it into the microwave rapid reaction system, react at a power of 250w and a temperature of 230°C for 12min; Filter and wash three times with distilled water to obtain the crude product. Recrystallize the crude product with 100mL of ethylene glycol, filter it with suction, put the product in a drying oven at 85°C, and bake it for 1.5h to obtain a yellow powder compound, namely 2,2'-bisbenzimidazole;
[0075] (2) Zn(NO 3 ) 2 ·6H 2 O (0.75mmol), 2,2'-bisbenzimidazole (0.25mmol), 5-hydroxyisophthalic acid (0.50mmol) and 20mL water were placed in a beaker, and then the pH value of the solution was adjusted with triethylamine to 9.0, stir evenly to form a raw material solution, the stirring time is 5m...
Embodiment 3
[0095] One, preparation method of the present invention:
[0096] (1) The preparation method of 2,2'-bisbenzimidazole is as follows: Weigh 2.13 grams (15 mmol) of ammonium oxalate and 3.24 grams of o-phenylenediamine (30 mmol) as reactants, add 23 mL of glycerol, and mix well Finally, put it into the microwave rapid reaction system and react for 15 minutes at a power of 230w and a temperature of 250°C; then react at a power of 320w and a temperature of 160°C for 12 minutes. Filter and wash twice with distilled water to obtain the crude product. Recrystallize the crude product with 100mL of ethylene glycol, filter it with suction, put the product in a drying oven at 90°C, and bake it for 1 hour to obtain a yellow powdery compound that is 2,2'-bisbenzimidazole;
[0097] (2) Zn(NO 3 ) 2 ·6H 2 O (0.5mmol), 2,2'-bisbenzimidazole (0.25mmol), 5-hydroxyisophthalic acid (0.5mmol) and 20mL water were placed in a beaker, and then the pH value of the solution was adjusted with triethy...
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