Tetravalent platinum complex containing BET inhibitor and application
An inhibitor, tetravalent platinum technology, applied in the field of medicine, can solve problems such as unclear mechanism, and achieve the effect of solving drug resistance, excellent in vitro anti-tumor activity, and excellent synergistic anti-tumor effect
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Embodiment 1
[0037] Synthesis of compound 1:
[0038]
[0039] Take 1.0 g of cisplatin, compound II, and add 25 mL of 30% hydrogen peroxide, react at 60° C. for 2 h, filter with suction, and leave the filtrate to obtain 0.95 g of oxoplatin, compound III, as a yellow needle-like solid, with a yield of 85%.
[0040]
[0041] Compound IV (purchased from Jilin Zhongke Shen Technology Co., Ltd., 30mg, 0.075mmol), TBTU (31mg, 0.095mmol) and triethylamine (9.5mg, 0.095mmol) were sequentially added to 2mL of dry DMF, stirred at room temperature for 10min , added compound III (25mg, 0.075mmol), and stirred at room temperature for 12h under nitrogen protection. After the reaction, the solvent was evaporated to dryness, and the residue was purified by silica gel column chromatography (DCM:MeOH=20:1) to obtain compound 1 as a white solid (38 mg, yield 70%).
Embodiment 2
[0043] Synthesis of Compound 2
[0044]
[0045] Compound 1 (30mg, 0.042mmol) and compound IV (17mg, 0.043mmol) were added to DMF (2mL), HBTU (19mg, 0.05mmol) and DIPEA (6.5mg, 0.05mmol) were added, and the reaction was stirred at room temperature for 12h After the reaction, the solvent was evaporated to dryness, and the residue was purified by silica gel column chromatography to obtain light yellow solid compound 2 (22 mg, yield 48%).
Embodiment 3
[0047] Synthesis of Compound 3
[0048]
[0049] Compound 1 (30mg, 0.042mmol) and acetic anhydride (5.1mg, 0.050mmol) were dissolved in DMF (2mL) for reaction. After 12 hours of reaction, the solvent was evaporated to dryness, and the residue was purified by silica gel column chromatography to obtain a white solid compound 3 (22 mg, yield 69%).
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