Method for compounding tri-substituted pyridine derivatives
A derivative and three-substitution technology, applied in the field of synthesis of pyridine derivatives, can solve the problems of difficult by-products, harsh reaction conditions, high reaction temperature, etc., and achieve the effects of easy separation and purification, mild reaction conditions, and simple operation
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Embodiment 1
[0023] The preparation of 2,6-diphenyl-4-p-picoline: add acetophenone 1mmol (120mg), p-methylbenzylamine 0.75mmol (91.6mg), catalyst HOTf0.05mmol (7.5mg) in the reaction vessel . React in an oil bath at 120°C for 24 hours, cool to room temperature, add water to quench the reaction, wash three times with ethyl acetate, separate the layers, combine the organic layers, decolorize with activated carbon, filter, dry over anhydrous sodium sulfate, concentrate under reduced pressure, and the product passes through Purified by column chromatography, the eluent was petroleum ether:ethyl acetate=50:1 (v / v), and a white solid product was obtained with a yield of 92% and a purity of 99.9%. 1 HNMR (400MHz, DMSO- d 6 ) δ ppm: δ8.33(d, J =7.2Hz, 4H), 8.18(s, 2H), 7.96(d, J =8.4Hz, 2H), 7.49-7.58(m, 6H), 7.38(d, J =8.0Hz, 2H); 13 CNMR (100MHz, DMSO- d 6 ) δ ppm: δ156.4, 149.9, 139.5, 139.3, 135.2, 130.2, 129.7, 129.2, 127.6, 127.4, 116.7, 21.3; HRMS (EI) Calcd.forC 24 h 19 N:[M +...
Embodiment 2
[0025] The preparation of 4-(4-fluorophenyl)-2,6-diphenylpyridine: add acetophenone 1mmol (120mg), p-fluorobenzylamine 0.75mmol (93.8mg), catalyst HOTf0.05mmol ( 7.5mg). React in an oil bath at 120°C for 24 hours, cool to room temperature, add water to quench the reaction, wash three times with ethyl acetate, separate the layers, combine the organic layers, decolorize with activated carbon, filter, dry over anhydrous sodium sulfate, concentrate under reduced pressure, and the product passes through Purified by column chromatography, the eluent is petroleum ether:ethyl acetate=50:1 (v / v), to obtain a white solid product with a yield of 78% and a purity of 99.8% 1 HNMR (400MHz, DMSO- d 6 ) δ ppm: δ8.36(d, J =7.6Hz, 4H), 8.21(s, 2H), 8.15(q, 2H), 7.49-7.60(m, 6H), 7.43(t, 2H); 13 CNMR (100MHz, DMSO- d 6 ) δ ppm: δ164.7, 162.2, 157.0, 148.9, 139.2, 134.6, 130.1, 129.7, 129.2, 127.4, 116.5; HRMS (EI) Calcd.forC 23 h 16 NF: [M + ], 325.1267. Found: m / z 325.1268.
Embodiment 3
[0027]The preparation of 2,6-diphenyl-4-m-picoline: add acetophenone 1mmol (120mg), m-methylbenzylamine 0.75mmol (91.6mg), catalyst HOTf0.05mmol (7.5mg) in the reaction vessel . React in an oil bath at 120°C for 24 hours, cool to room temperature, add water to quench the reaction, wash three times with ethyl acetate, separate the layers, combine the organic layers, decolorize with activated carbon, filter, dry over anhydrous sodium sulfate, concentrate under reduced pressure, and the product passes through Purified by column chromatography, the eluent was petroleum ether: ethyl acetate = 50:1 (v / v), to obtain a white solid product with a yield of 91% and a purity of 99.9%. 1 HNMR (400MHz, CDCl 3 ) δ ppm: δ8.22(d, J =7.6Hz, 4H), 7.87(q, 2H), 7.41-7.55(m, 9H), 7.29(s, 1H); 13 CNMR (100MHz, CDCl 3 ) δ ppm: δ157.5, 150.4, 139.7, 139.1, 138.9, 129.8, 129.1, 128.8, 128.0, 127.2, 127.2, 124.4, 117.2, 21.6; HRMS (EI) Calcd.forC 24 h 19 N:[M + ], 321.1517. Found: m / z 321.1519....
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