(2-pyridinecarbaldehyde)-2,6 pyridine bisacylhydrazone copper compound, preparation method and application thereof
A technology of pyridine bisacylhydrazone copper and pyridine bisacylhydrazone, which is applied in the field of preparation of -2,6 pyridine bisacylhydrazone copper compound, and achieves the effects of good fat solubility, high anticancer activity and simple preparation method
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Embodiment 1
[0016] The steps are: 0.25mmol (2-pyridinecarbaldehyde)-2,6 pyridine bisacylhydrazone (H 2 L) (92.8mg) and 0.75mmolCu(NO 3 )·3H 2 O (181mg) was dissolved in 20mL of methanol, stirred at room temperature for 5h, filtered, and the filtrate was placed in 6 test tubes at an average of 3ml each, and diffused with ethanol and ether. After one week, dark green flaky crystals were obtained, and the yield of 6 test tubes was 64.93 mg, yield 28.4%. Melting point greater than 300 ° C. The highest yield of this compound was 68.6%.
[0017] The copper compound of the present invention is analyzed through X-single crystal diffraction, and gained crystallographic data is as follows: this compound belongs to monoclinic system, and space group is P2(1) / n, and unit cell parameter is: a = 11.3200(9)Å, b = 13.2506(11) Å, c =30.683(3) Å, α =90°, β =92.639(2) °, gamma = 90°, V =3021.4(4) Å 3 , Z = 4, D c =1.930Mg·m -3 , μ =2.194mm -1 , F(000) =1756, 2.52 3 , the independent...
Embodiment 2
[0019] 0.2mmo(2-pyridinecarbaldehyde)-2,6pyridine bisacylhydrazone (H 2 L) and 0.6mmol Cu(NO 3 )·3H 2 O mixed and dissolved in 15mL of methanol, stirred at room temperature for 5h, filtered, the filtrate evaporated, the filtrate was placed in 5 test tubes with an average of 3ml each, and ethanol and ether were added dropwise to diffuse. After 5 days, dark green flaky crystals were obtained, with a melting point greater than 300°C . The highest yield of this compound was 67.0%.
Embodiment 3
[0021] 0.15mmo(2-pyridinecarbaldehyde)-2,6pyridine bisacylhydrazone (H 2 L) and 0.45mmol Cu(NO 3 )·3H 2 O mixed and dissolved in 15mL of methanol, stirred at room temperature for 8h, filtered, and the filtrate was volatilized, and the filtrate was placed in 5 test tubes with an average of 3ml each, and diffused by dropping ethanol and ether. After 4 days, dark green flaky crystals were obtained, with a melting point greater than 300°C . The highest yield of this compound was 66.1%.
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