Bipiperidine substituted isoflavone compound and uses thereof
A technology of compound and composition, applied in the field of isoflavone compounds substituted by bispiperidine
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[0039] 1. Preparation of Compound I
[0040] Synthesis of 3-(4-methoxyphenyl)-7-(4-bromobutoxy)-4H-chromogen-4-one (2)
[0041] In a 1000mL single-mouth flask, add formononetin (5g, 18.6mmol), finely ground anhydrous potassium carbonate powder (30g, 217mmol), 500mL acetone, and then add 1,4-dibromobutane (24mL, 198mmol) ), the reaction mixture was heated under reflux for 10 hours, the reaction mixture was concentrated under reduced pressure, the residue was added with water, stirred, and filtered with suction. The filter cake was washed with water and dried to obtain 6.62 g of white solid with a yield of 88.6%. mp: 152.8-154.0°C. 1H NMR (400MHz, CDCl3) δ: 8.21 (d, J = 8.8Hz, 1H), 7.91 (s, 1H), 7.50 (d, J = 8.8Hz, 2H), 6.99-6.96 (m, 3H), 6.84 (d,J=2.4Hz,1H),4.10(t,J=6.0Hz,2H),3.84(s,3H),3.51(t,J=6.0Hz,2H),2.14-1.98(m,4H) ; 13C NMR (100MHz, CDCl3) δ: 175.8, 163.2, 159.6, 157.9, 152.0, 130.1, 127.8, 124.9, 124.2, 118.5, 114.7, 114.0, 100.6, 67.6, 55.3, 33.2, 29.3, 27.6. ESI-MS ( m...
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