Method for synthesizing anticancer compound Na4Bi2Mn2W20C6H84N4O105
A na4bi2mn2w20c6h84n4o105, synthetic method technology, applied in the field of synthesis of anticancer compounds, to achieve good inhibition rate, strong proliferation inhibition effect
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specific Embodiment approach 1
[0008] Embodiment 1: The anticancer compound Na of this embodiment 4 Bi 2 Mn 2 W 20 C 6 H 84 N 4 O 105 The synthesis method of the compound is realized according to the following steps: 1. Under magnetic stirring, 4-5 mmol of Na 2 WO 4 Dissolve in 80~120ml deionized water, heat to 80~120℃, then add 6mol / L HCl dropwise to adjust pH to 5.0~7.0 to obtain solution A; 2. Put 0.5~1mmol 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, it was added to solution A, mixed and heated to 80-120 °C for 1-2 hours, then cooled to room temperature, filtered and left to stand 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 The synthesis of ; wherein the consumption of HCl in step 2 is 10mL.
[0009] The anticancer compound Na obtained in this embodiment 4 Bi 2 Mn 2 W 20 C 6 H 84 N 4 O 105 For the yellow bulk crystals.
[0010] The cooling in step 2 of this emb...
specific Embodiment approach 2
[0011] Embodiment 2: The difference between this embodiment and Embodiment 1 is that in step 1, 4 mmol of Na 2 WO 4 Dissolve in 80 ml of deionized water and heat to 80°C. Other steps and parameters are the same as in the first embodiment.
specific Embodiment approach 3
[0012] Embodiment 3: The difference between this embodiment and Embodiment 1 is that in step 1, 5 mmol of Na 2 WO 4 Dissolve in 120 ml of deionized water and heat to 120°C. Other steps and parameters are the same as in the first embodiment.
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