Method for synthesizing anticancer compound Na4Bi2Mn2W20C6H84N4O105
A technology of na4bi2mn2w20c6h84n4o105 and a synthesis method is applied in the field of synthesis of anticancer compounds to achieve the effect of strong proliferation inhibition and good inhibition rate
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specific Embodiment approach 1
[0008] Specific embodiment one: the anticancer compound Na of this embodiment 4 Bi 2 mn 2 W 20 C 6 h 84 N 4 o 105 The synthetic method of is realized according to the following steps: one, under magnetic stirring, the Na of 4~5mmol 2 WO 4 Dissolve in 80-120ml of deionized water, and heat to 80-120°C, then add 6mol / L HCl dropwise to adjust the pH to 5.0-7.0 to obtain solution A; 2. Mix 0.5-1mmol of MnCl 2 , 0.8-1.2 mmol of solid imidazole and 0.3-0.8 mmol of Bi(NO) dissolved in 6 mol / L HCl 3 ) 3 At the same time, add it to solution A, mix it and heat it to 80-120°C for 1-2 hours, then cool it to room temperature, filter it and let it rest for 5-10 days to complete the anticancer compound Na 4 Bi 2 mn 2 W 20 C 6 h 84 N 4 o 105 Synthesis; wherein the amount of HCl in step 2 is 10mL.
[0009] The obtained anticancer compound Na in the present embodiment 4 Bi 2 mn 2 W 20 C 6 h 84 N 4 o 105 It is yellow blocky crystal.
[0010] The cooling in the second st...
specific Embodiment approach 2
[0011] Specific implementation mode 2: The difference between this implementation mode and specific implementation mode 1 is that in step 1, 4~? mmol Na 2 WO 4 Dissolve in 80ml of deionized water and heat to 80°C. Other steps and parameters are the same as those in Embodiment 1.
specific Embodiment approach 3
[0012] Specific embodiment three: the difference between this embodiment and specific embodiment one is that in step one, 5 mmol of Na 2 WO 4 Dissolve in 120ml of deionized water and heat to 120°C. Other steps and parameters are the same as those in Embodiment 1.
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