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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

Inactive Publication Date: 2020-04-14
JINAN UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

It has been reported in many literatures that the introduction of DG is relatively easy, but the conditions for removing DG are quite harsh. For example, these conditions generally require the use of particularly active metals such as sodium or potassium, and they are still under high temperature conditions. In these literatures, a lot of risk factors have been subtly added to the experiment. What is more serious is that the conditions of these reactions are difficult to achieve in the stage of mass production in practical application. If the company follows this traditional old method to In terms of operation, even small batches of gram-level reactions are difficult to achieve

Method used

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  • A class of o-aminophenol derivatives and preparation method thereof
  • A class of o-aminophenol derivatives and preparation method thereof
  • A class of o-aminophenol derivatives and preparation method thereof

Examples

Experimental program
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Effect test

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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Abstract

The invention first discloses a preparation method of an ortho-aminophenol derivative. The preparation method comprises the following steps: (1) by adopting an aryl amine compound as a substrate and 2-chloro-5-nitropyridine as a guiding base, reacting in acetonitrile, thus obtaining a pyridine aryl amine compound intermediate; (2) catalyzing the pyridine aryl amine compound intermediate in step (1) to make C-H activation reaction in a solvent by using iodobenzene diacetate as an oxidant and palladium acetate as a catalyst, thus obtaining an acetoxylation aniline derivative, draining, and thenperforming the chromatographic separation and purification; and (3) enabling the acetoxylation aniline derivative in step (2) to react in a tetrahydrofuran solvent for 30 min at a normal temperature by virtue of hydrazine hydrate, thus obtaining the ortho-aminophenol derivative, quenching, washing, extracting, drying, draining, and performing the chromatographic separation and purification. The invention also discloses the ortho-aminophenol derivative prepared by the method.

Description

technical field [0001] The invention belongs to the field of chemical synthesis, and in particular relates to a class of o-aminophenol derivatives and a preparation method thereof. Background technique [0002] In recent years, with the rise of transition metal-catalyzed C–H bond functionalization, directing groups assist C sp2 -H bond functionalization has attracted extensive attention. Various directing groups such as amines, imines, oximes, diazenes, amides, pyridines, pyrimidines, carboxylic acids, etc., were used to achieve regioselective C–H functionalization. Although the introduction and removal of the introducing group usually adds two steps to the overall synthesis, it can become more manipulable if the directing group (DG) is only briefly attached to the substrate molecule during the functionalization step. However, only very limited success examples have been obtained, and only a few reports have been recorded, and the substrates are limited to amines and forma...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07D239/42C07C213/00C07C215/76C07D401/04C07D403/12C07D409/12C07D401/12
CPCC07C213/00C07C215/76C07D239/42C07D401/04C07D401/12C07D403/12C07D409/12
Inventor 冯鹏举陈填烽陈俊丰黄译锋
Owner JINAN UNIVERSITY
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