A class of o-aminophenol derivatives and preparation method thereof
A technology for o-aminophenol and derivatives, applied in the field of o-aminophenol derivatives and their preparation, can solve problems such as being difficult to achieve mass production, difficult to realize, etc., and achieve a wide range of substrates, convenient operation, and high price. cheap effect
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Embodiment 1
[0033] Embodiment 1, the preparation method of synthetic 2-((5-nitropyrimidin-2-yl) amino) phenyl acetate
[0034] Step 1: Vacuumize a dry 50mL reaction flask with nitrogen three times, then add aniline (93.1mg, 1.0mmol, 1.0equiv) to the reaction flask, add 10.0mL of dried acetonitrile and stir until the aniline is completely Dissolve, and then add 2-chloro-5-nitropyrimidine (0.1593g, 1.0mmol, 1.0equiv) into the reaction eggplant bottle. The whole mixture was reacted under nitrogen pressure for 4-5 hours. The process of the reaction was detected by TLC, if it was detected that all the aniline had reacted completely, the reaction could be stopped. The experimental treatment is to drain the solution in the reaction; dissolve the solute in the reaction bottle with ethyl acetate, and transfer it to a 100mL round-bottomed flask, add 2mL (200-300 mesh) of silica gel spinner to the round-bottomed flask Dry with (petroleum ether and ethyl acetate) through silica gel on the column. ...
Embodiment 2
[0040] Embodiment 2, the method for the preparation of synthetic 3-methyl-2-((5-nitropyrimidin-2-yl) amino) phenyl acetate
[0041]The first step: vacuumize a dry 50mL reaction eggplant bottle with nitrogen three times, then add o-toluidine (107mg, 1.0mmol, 1.0equiv) to the reaction eggplant bottle, add 10.0mL of dried acetonitrile and stir until the aniline Completely dissolved, and then added 2-chloro-5-nitropyrimidine (0.1593g, 1.0mmol, 1.0equiv) into the reaction eggplant bottle. The whole mixture was reacted under nitrogen pressure for 5 hours. The process of the reaction was detected by TLC, if it was detected that all the aniline had reacted completely, the reaction could be stopped. The experimental treatment is to drain the solution in the reaction; dissolve the solute in the reaction bottle with ethyl acetate, and transfer it to a 100mL round-bottomed flask, add 2mL (200-300 mesh) of silica gel spinner to the round-bottomed flask Dry with (petroleum ether and ethyl...
Embodiment 3
[0047] Embodiment 3, the method for the preparation of synthetic 4-methyl-2-((5-nitropyrimidin-2-yl) amino) phenyl acetate
[0048] Step 1: Vacuumize a dry 50mL reaction flask with nitrogen three times, then add aniline (107mg, 1.0mmol, 1.0equiv) to the reaction flask, add 10.0mL of dried acetonitrile and stir until m-toluidine Completely dissolved, and then added 2-chloro-5-nitropyrimidine (0.1593g, 1.0mmol, 1.0equiv) into the reaction eggplant bottle. The whole mixture was reacted under nitrogen pressure for 4-5 hours. The process of the reaction was detected by TLC, if it was detected that all the aniline had reacted completely, the reaction could be stopped. The experimental treatment is to drain the solution in the reaction; dissolve the solute in the reaction bottle with ethyl acetate, and transfer it to a 100mL round-bottomed flask, add 2mL (200-300 mesh) of silica gel spinner to the round-bottomed flask Dry with (petroleum ether and ethyl acetate) through silica gel ...
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