Synthesis of zinc phenanthroline aminopolycarboxylate complex and application of complex in anti-tumor drugs
An aminopolycarboxylic acid, o-phenanthroline technology, applied in antitumor drugs, zinc organic compounds, drug combinations, etc. Problems such as drug resistance and poor water solubility of drugs are generated, and the effects of simple preparation method, small toxic and side effects, and fast precipitation time are achieved.
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Embodiment 1
[0019] Example 1: Add 1.5mmol o-phenanthroline, 2.5mmol iminodiacetic acid, and 2.5mmol zinc nitrate to a 50mL round-bottomed flask in sequence, stir and react at 80°C for 0.5h, and adjust the pH value to 4.0; filter, and place the filtrate in In a beaker, naturally volatilize to obtain the zinc complex of o-phenanthroline iminodiacetic acid ( Zn-ida complex ) as white crystals, the compound yield was 61%.
[0020] The product is analyzed by infrared spectroscopy, and the structure is as follows: IR (KBr, cm -1 ): V as (CO 2 ) 1625 vs, 1597 vs , 1518 m; V s (CO 2 ) 1426 m, 1387 s, 1297 m
[0021] The product was analyzed by elements, and the data are as follows: Experimental value (%): C, 47.30; H, 3.90; N, 12.33. Calculated value (%): C, 47.26; H, 3.87; N, 12.40.
Embodiment 2
[0022] Example 2: Add 1.0mmol o-phenanthroline, 1.5mmol iminodiacetic acid, and 1.0mmol zinc chloride successively to a 50mL round-bottomed flask, stir and react at 80°C for 1.0h, and adjust the pH value to 4.0; filter, and place the filtrate in into a beaker, naturally volatilized to obtain white crystals, and the compound yield was 56%.
Embodiment 3
[0023] Example 3: Add 2.0mmol o-phenanthroline, 1.5mmol iminodiacetic acid, and 1.5mmol zinc sulfate to a 50mL round bottom flask in sequence, stir and react at 80°C for 1.5h, and adjust the pH value to 2.0; filter, and place the filtrate in In the beaker, white crystals were obtained by natural volatilization, and the compound yield was 55%.
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