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Preparation method of 2-azanoradamantane-N-Oxyl

A non-adamantane, free radical technology, applied in the field of preparation of Nor-AZADO, can solve the problems of not strictly optimized reaction conditions parameters, limited application and promotion, too many acidic wastewater, etc., and achieves easy industrialized large-scale production and great economic value. and social values, mild and safe effects of reaction conditions

Active Publication Date: 2017-02-01
深圳市宏辉浩医药科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In the synthetic route of the prior art, the first step uses acetic acid and water as the solvent of the reaction system, the reaction process is messy, the purity of the target product obtained is not high, and the acid waste water produced is more difficult to handle; the second step uses giant Toxic and carcinogenic benzene is used as a reaction solvent, which is basically banned in R&D and production; the third step is to use sodium-hydrogen to form a salt, and sodium-hydrogen is extremely active, and the reaction process produces flammable and explosive hydrogen gas, which increases research and development. and production hazards, and use N,N-dimethylformamide (referred to as "DMF") as a solvent, which is difficult to recycle, produces a large amount of nitrogen-containing wastewater, and endangers the environment; the parameters of the fourth and fifth step reaction conditions are not strictly optimized , the yield is low, the yield of the whole route is only 13.2%, and a large amount of waste is generated
[0006] Therefore, the Nor-AZADO preparation method of the prior art cannot carry out large-scale commercial production, and only a small amount of reagents are provided at present, limiting its application and promotion in the fine chemical industry field of the pharmaceutical industry

Method used

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  • Preparation method of 2-azanoradamantane-N-Oxyl
  • Preparation method of 2-azanoradamantane-N-Oxyl

Examples

Experimental program
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Effect test

example 1

[0048] In said step 1, the compound 9-benzyl-9-azabicyclo-[3,3,1]nonan-3-one was prepared according to the following scheme:

[0049] Benzylamine (5.0g, 47mmol) and Na 2 HPO 4 12H 2 O (5.0g) was dissolved in 50ml of water, acetone dicarboxylic acid (3.5g, 24mmol, 1.2eq) was added, and a concentration of 25% glutaraldehyde (8g, 20mmol, 1.0eq) was added dropwise in an ice-water bath, and maintained After 60 minutes, rise to room temperature and react for 24 hours, then dropwise add concentrated hydrochloric acid to adjust the pH value to 3, stir and react in an oil bath at 50°C for 2 hours, cool to room temperature, and adjust the pH value to 10 with 20% NaOH solution. Then extract twice with dichloromethane, combine the organic phases, wash the organic phase once with saturated brine, and concentrate under reduced pressure to obtain 9-benzyl-9-azabicyclo-[3,3,1]nonan-3-one soil The crude yellow solid was crystallized and purified with ethyl acetate and petroleum ether at a v...

example 2

[0051] In said step 1, the compound 9-benzyl-9-azabicyclo-[3,3,1]nonan-3-one was prepared according to the following scheme:

[0052] Benzylamine (50g, 1.2eq) and Na 2 HPO 4 12H 2 O (40.83g, 0.4eq) was dissolved in 400mL of water, acetone dicarboxylic acid (35g, 240mmol, 1.2eq) was added to adjust the pH value to 4.8-5.2, and a concentration of 25% glutaraldehyde ( 80g, 200mmol, 1eq), and maintained for 30 minutes, raised to room temperature and reacted for 24 hours, added dropwise concentrated hydrochloric acid to adjust the pH value to 3, then stirred and reacted in 70°C oil bath for 1 hour, after the reaction was cooled to room temperature, used 20% NaOH solution adjusted the pH value to 10, filtered, the filtrate was extracted twice with dichloromethane, the organic phases were combined, the organic phase was washed once with saturated brine, and concentrated under reduced pressure to obtain a reddish-brown oil, with a volume ratio of 1: 5 ethyl acetate and petroleum et...

example 3

[0054] In the step 1, the compound 9-benzyl-9-azabicyclo-[3,3,1]nonan-3-one was prepared according to the following scheme.

[0055] Add 400g of disodium hydrogen phosphate, 300g of citric acid, and 3.2Kg of deionized water into a 10L reaction bottle, stir at room temperature for 20 minutes, use ice salt to adjust the temperature to about 5°C, and then add 1000g of glutaraldehyde with a concentration of 25% at one time , control the reaction temperature below 10°C, add 537g of benzylamine hydrochloride, adjust the pH value between 4.5-5.5, add 500g of acetone dicarboxylic acid in batches, control the reaction temperature at about 10°C, and a small amount of bubbles will be generated. After the addition is complete, use 20% NaOH solution to adjust the pH value to about 4.8-5.2, stir overnight at room temperature, add concentrated hydrochloric acid dropwise to adjust the pH value to 2-3, then stir and react in an oil bath at 55°C for 1 hour, and wait for the reaction to cool Aft...

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Abstract

The invention discloses a preparation method of 2-azanoradamantane-N-Oxyl (Nor-AZADO). The method comprises the following steps: placing acetonedicarboxylic acid, glutaraldehyde and benzylamine in an aqueous hydrophosphate solution, and carrying out condensation and decondensation to obtain 9-benzyl-9-azabicyalo-[3,3,1]-nonyl-3-one; carrying out condensation dehydration on 9-benzyl-9-azabicyalo-[3,3,1]-nonyl-3-one and benzene or benzene ring substituted sulfohydrazide, and adding an alkali to obtain 2-(9-benzyl-9-azabicyalo-[3,3,1]-nonane-3-ylidene)-1-benzene or benzene ring substituted sulfohydrazide sodium / potassium salt; carrying out refluxing ring closing on the 2-(9-benzyl-9-azabicyalo-[3,3,1]-nonane-3-ylidene)-1-benzene or benzene ring substituted sulfohydrazide sodium / potassium salt in an organic solvent to obtain N-benzyl-2-azanoradamantane; debenzylating N-benzyl-2-azanoradamantane to obtain 2-azanoradamantane; and oxidizing 2-azanoradamantane by a peroxide oxidant to obtain the Nor-AZADO. The preparation method has the advantages of great increase of the synthesis yield, greenness and environmental protection, high efficiency, low cost, and easiness in industrial large-scale production.

Description

technical field [0001] The invention relates to catalyst organic synthesis technology, in particular to a preparation method of Nor-AZADO. Background technique [0002] 2-Azanonadamantane N-Oxyl (2-Azanoradamantane N-Oxyl, Nor-AZADO) is an unpaired N, N-disubstituted N-oxyl radical. It can exist stably, and can be widely used in the production process of oxidizing alcohol. In the process of catalyzing the oxidation of alcohol, it has super high catalytic activity and catalytic ability. European Patent No. EP2594550 describes in detail the synthesis method of Nor-AZADO as a catalyst to oxidize alcohols to aldehydes and ketones. In the synthesis method, sodium hypochlorite and air are used as oxidants, and alcohols are oxidized into aldehydes or ketones under the condition of 0 degrees to room temperature; the method is mild and safe, and the by-products are environmentally friendly and non-toxic, meeting the requirements of the current pharmaceutical industry and fine chemic...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D471/08
CPCC07D471/08
Inventor 王灿辉童建宏侯利媛
Owner 深圳市宏辉浩医药科技有限公司
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