Bifendate derivative containing halogen substituent, preparation method and application
A bifendate, halogen-containing technology, applied in the field of chemical medicine, can solve the problems of inability to achieve healing effect, rebound, etc.
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Embodiment 1
[0293] Example 1: 4,4'-dimethoxy-5,6,5',6'-two methylenedioxy-2,2'-biphenyl dicarboxylic acid (compound 2)
[0294] 10g of 4,4'-dimethoxy-5,6,5',6'-dimethoxy-2,2'-biphenyl dicarboxylate (compound 1) 10g, add 15g KOH and 300ml water, Heat to reflux for 6 hours, TLC detects that the reaction is complete, cool to room temperature and filter to remove insoluble matter, adjust the pH to 2 with concentrated hydrochloric acid, at this time a large amount of white solid powder precipitates, filter and wash with water until neutral, and vacuum dry to obtain 8.34g of white solid powder , yield 89.5%. 1 H-NMR (d 6 -DMSO, 400MHz) δ: 3.88(s, 6H), 5.96(s, 2H), 5.99(s, 2H), 7.26(s, 2H), 12.36(s, 2H).MS(ESI, m / z) : 389.19[M-H] - .
Embodiment 2
[0295] Example 2: Preparation of 4,4'-dimethoxy-5,6,5',6'-dimethoxy-2,2'-biphenyl dicarboxylic anhydride (compound 3)
[0296] Add 50ml of acetic anhydride to 8.3g of compound 2, heat and reflux for 12h, cool to room temperature after the reaction is complete, spin off the solvent to obtain a light yellow solid powder, add the obtained solid powder to 50ml of anhydrous toluene, mix well, filter with suction, and wash with anhydrous toluene Three times, 6.1 g of white solid powder was obtained, with a yield of 73.6%. The obtained product was directly used in the next reaction without further purification.
Embodiment 3
[0297] Example 3: Preparation of 4,4'-dimethoxy-5,6,5',6'-dimethoxy-2-methoxycarbonyl-2'-carboxylic acid biphenyl (compound 4)
[0298] Weigh 6.1g of compound 3, add 200ml of methanol, add reflux for 10h, TLC detects that the reaction is complete, cool to room temperature, spin off most of the methanol, filter with suction, wash the filter cake twice with ethanol, and dry to obtain 5.9g of white solid powder , yield 96.7%. 1 H-NMR (d 6 -DMSO, 400MHz) δ: 3.58(s, 3H), 3.89(s, 6H), 5.97-6.01(m, 4H), 7.24(s, 1H), 7.27(s, 1H), 12.34(s, 1H) .MS (ESI, m / z): 427.16 [M+Na] + .
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