Process of synthesizing fexofenadine intermediate
A synthesis method and technology of ligands are applied in the field of synthesis of intermediates of fexofenadine, which can solve the problems of high environmental control pressure, harm to human body, difficult control and the like, and achieve low environmental pollution, short reaction period and product quality. Good results
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Embodiment 1
[0041] Embodiment 1: 4-[4-[4-(hydroxyl diphenylmethyl)-1-piperidinyl]-butenyl]-α, the synthesis of α-dimethylphenylacetic acid methyl ester
[0042] Its reaction equation is:
[0043]
[0044] 4.45g (495g / mol, 8.99mmol) starting material (IV), 300ml ethanol, 0.38g 5%Pd / CaCO 3 successively added to a 500ml three-necked flask. After stirring at room temperature, 20 drops of quinoline (about 1 ml) were added dropwise. Stirring was stopped, and the air in the system was replaced with nitrogen for 3 times, and hydrogen for 1 time. Keep the hydrogen pressure at 0.02MPa, stir and react at 30°C for 10h, stop the reaction, vent, filter, concentrate and refine to obtain 4.02g of product (V). The conversion rate reaches 90%. 1 H NMR (CDCl 3 ): 7.1~7.5(aromatics, 14H), 6.40(d, 1H), 5.60(m, 1H), 3.63(s, 3H), 2.95(d, 2H), 2.41~2.52(m, 5H), 1.94~ 1.98 (m, 2H), 1.56 (s, 6H), 1.46~1.51 (m, 4H).
Embodiment 2
[0045] Example 2: (±)-4-[1-hydroxyl-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-butyl]-a,a-dimethylphenylacetic acid methyl Synthesis of esters
[0046] Its reaction equation is:
[0047]
[0048] Compound (V) 4.02g (497g / mol, 8.09mmol), manganese acetate (0.64mmol), Schiff base ligand (0.64mmol) and NaBH 4 (16.18mmol) add 150ml of mixed solvent of toluene and ethanol (1:1), at room temperature and normal pressure, stir and introduce oxygen to react for 4 hours, point the plate to track, after the reaction of the reactant is complete, remove the ethanol under reduced pressure, add water to wash the organic phase, the organic phase was dried with magnesium sulfate, filtered and the filtrate was taken, and the solvent was removed to obtain a crude product. 3.65 g of the target product (I) was obtained by column separation with a yield of 90%. 1 HNMR (CDCl 3 ): 7.1~7.5(aromatics, 14H), 4.59(d, 1H), 3.15(d, 1H), 2.98(d, 1H), 2.40~2.50(m, 4H), 2.1(t, 1H), 2.00( t, 1H), 1.48...
Embodiment 3
[0050] The reaction solvent was changed to methanol, and the others were the same as in Example 1 to obtain 3.98 g of product (V) (yield 89%).
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