Platinum (II) complex, synthetic method and application thereof
A synthetic method and compound technology applied in the field of medicine to achieve good medicinal value and significant anti-tumor activity in vitro
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Embodiment 1
[0042] Accurately weigh 0.5 mmol of ligand L and 0.5 mmol of dichlorobis(dimethylsulfoxide) platinum (II), dissolve ligand L in 35 mL of 85% methanol, and dichloro Two (dimethyl sulfoxide) platinum (II) was dissolved in 20 mL of water, the two solutions were mixed, refluxed at 65 ° C for 36 hours, concentrated and evaporated to remove most of the solvent (75% of the solvent added), cooled After standing at room temperature, the reddish-brown target product was precipitated, and reddish-brown bulk crystals were precipitated after the filtrate was placed for 3 days, and the crystals and powder were collected to obtain the final product (96% yield, the product is the total mass of powder and crystals, the same below).
[0043] The resulting reddish-brown solid product is identified:
[0044] (1) Infrared spectrum:
[0045] IR(KBr):3412,3061,2968,2926,1585,1530,1478,1464,1421,1354,1266,1246,1216,1156,1124,1076,1040,1009,890,818,779,733,716,687,4651,62 -1 .
[0046] (2) Proton N...
Embodiment 2
[0059] Accurately weigh 0.5 mmol of ligand L and 0.5 mmol of dichlorobis(dimethylsulfoxide) platinum (II), and dissolve ligand L in a mixture of 95 mL of 75% methanol and 25% ethanol Solution (the volume ratio of methanol and ethanol is 5:1), dichloro two (dimethyl sulfoxide) platinum (II) is dissolved in the mixed solution of the water of 40mL and 90% methanol (volume of water and methanol ratio of 1:9), the two solutions were mixed, reflux reaction at 85 ° C for 24 hours, concentrated and evaporated to remove most of the solvent (90% of the solvent added), cooled to room temperature and left to stand, and the reddish-brown target product was precipitated. After filtration, reddish-brown crystals were precipitated after standing for 3 days, and the powder and crystals were collected to obtain the final product (yield 75%).
[0060] The resulting final product was analyzed by infrared spectroscopy, hydrogen nuclear magnetic resonance spectroscopy, carbon nuclear magnetic reson...
Embodiment 3
[0062] The amount of accurately weighed substance is 0.5mmol of ligand L and 0.5mmol of dichlorobis(dimethyl sulfoxide) platinum (II), and the ligand L is dissolved in 60mL of dimethyl sulfoxide. Chlorobis(dimethyl sulfoxide) platinum (II) was dissolved in 15 mL of 90% acetone solution, the two solutions were mixed, refluxed at 45°C for 56 hours, concentrated and evaporated to remove most of the solvent (solvent addition amount 82%), cooled to room temperature and stood still, the reddish-brown target product was precipitated, and after filtering, reddish-brown crystals were precipitated after standing for 3 days, and the powder and crystals were collected to obtain the final product (yield 85%).
[0063] The resulting final product was analyzed by infrared spectroscopy, hydrogen nuclear magnetic resonance spectroscopy, carbon nuclear magnetic resonance spectroscopy, electrospray mass spectroscopy and X-ray single crystal diffraction, and was determined to be the target product...
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