Metal organic gold (iii) complexes and their synthesis methods and applications
A synthesis method and compound technology, applied in the field of medicine, can solve the problems that have not been found in activity research, and achieve the effects of cheap and easy-to-obtain reaction raw materials, good proliferation inhibitory activity, resistance to drug resistance, and high physiological stability
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Embodiment 1
[0021] Embodiment 1: the synthesis of target product Cyc-Au-1
[0022] Take KAuCl 4 (0.2mmol) and 3,4-dimethoxyphenethylamine (0.2mmol) are placed in the container, then add 30mL in the mixed solvent that is made up of dichloromethane and methanol (the volume ratio of dichloromethane and methanol is 1 : 1), the resulting mixture was refluxed and stirred for 24 hours under dark conditions, the resulting reactant was filtered, the filtrate was collected, and left to stand, yellow crystals were precipitated, the crystals were collected, and vacuum-dried to obtain a yellow solid product with a yield of 55%.
[0023] The product obtained in this embodiment is characterized:
[0024] 1) proton nuclear magnetic spectrum analysis, the obtained spectral data are as follows:
[0025] H NMR spectrum: 1 H NMR (400MHz, DMSO-d 6 )δ6.84(d,J=8.1Hz,1H),6.70(dd,J=8.1,1.6Hz,1H),3.74(s,3H),3.72(s,3H),2.81–2.67(t,J =5.4Hz 2H), 2.57(t, J=7.2Hz, 2H).
[0026] 2) Electrospray mass spectrometry ...
Embodiment 2
[0034] Embodiment 2: the synthesis of target product Cyc-Au-1
[0035] Example 1 was repeated except that the mixed solvent consisting of dichloromethane and methanol was replaced with chloroform. Yield 58%.
[0036] The product obtained in this example was analyzed by proton nuclear magnetic spectrum, electrospray mass spectrometry and X-ray single crystal diffraction, and it was determined that the product obtained in this example was the target product Cyc-Au-1.
Embodiment 3
[0037] Embodiment 3: the synthesis of target product Cyc-Au-1
[0038] Example 1 was repeated, except that the reaction was carried out at 25° C., and the reaction time was 48 hours. Yield 46%.
[0039] The product obtained in this example was analyzed by proton nuclear magnetic spectrum, electrospray mass spectrometry and X-ray single crystal diffraction, and it was determined that the product obtained in this example was the target product Cyc-Au-1.
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