Novel chemical synthesis method for adenine

A chemical synthesis, adenine technology, applied in the field of chemical synthesis of adenine, can solve the problems of many side reactions, difficult to obtain pure products, cumbersome post-processing, etc., achieve low production cost, shorten the route steps, and improve production efficiency.

Inactive Publication Date: 2013-01-23
YANGZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

Route 3 adopts the "one pot cooking" method, but there are many side reactions in actual production, the post...

Method used

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  • Novel chemical synthesis method for adenine
  • Novel chemical synthesis method for adenine
  • Novel chemical synthesis method for adenine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] Embodiment 1: the synthesis of raw material 4,6-dihydroxypyrimidine

[0052] Add 2500 mL of absolute ethanol to a 5000 mL three-necked round bottom flask equipped with stirring, and then slowly add 150 g of metallic sodium until the metallic sodium basically disappears to obtain a transparent solution. Begin to heat up slowly. Measure 200 mL of formamide, and slowly drop it into the sodium ethoxide solution with a constant pressure dropping funnel. At 65-70° C., continue to slowly add 310 mL of diethyl malonate dropwise after the drop, and the solution starts to turn white. After dropping, adjust the temperature to 110° C., and continue heating and stirring overnight. After the solution was cooled to room temperature, most of the ethanol was distilled off under reduced pressure. Then, the remaining residue was treated with a mixed solution of 450 mL of concentrated hydrochloric acid and 750 mL of ice water at 0°C. Suction filter, wash with ice water, and dry under r...

Embodiment 2

[0053] Example 2: Synthesis of 4,6-dihydroxy-5-nitropyrimidine

[0054]Pour 500mL of concentrated nitric acid and 100mL of concentrated sulfuric acid into a 2500mL three-neck flask equipped with stirring. Weigh 112g of 4,6-dihydroxypyrimidine, and add it to the mixed acid solution in batches under ice-bath conditions, and keep stirring. The solution turned dark red. After the addition, the reaction was continued at 0°C for 90 minutes, and then continued at room temperature for 3 hours. The reaction solution was poured into 5000 mL of crushed ice, solids were precipitated, filtered, washed with water, recrystallized from absolute ethanol, and dried in vacuo. 110 g of solid were obtained. The yield is about 70%.

Embodiment 3

[0055] Example 3: Synthesis of 4,6-dichloro-5-nitropyrimidine

[0056] Add 500mL POCI to the three-necked flask 3 , and then slowly added 80g of 4,6-dihydroxy-5-nitropyrimidine, heated to 50°C and added 100mL of N,N-dimethylaniline, heated to reflux for 2h. After the solution was cooled to room temperature, excess phosphorus oxychloride was recovered by distillation under reduced pressure. After concentration, the dark black solution obtained was poured into 5000 mL of ice water and extracted with ethyl acetate (3×500 mL). The organic layers were combined and dried over anhydrous magnesium sulfate. The ethyl acetate solution was concentrated under reduced pressure to obtain a black solid, which was recrystallized from petroleum ether at 60-90°C to obtain 75 g of yellow crystals, with a yield of about 76%.

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Abstract

The invention discloses a method for synthesizing adenine represented by a formula (I), wherein the method comprises the following steps of making formamide react with diethyl malonate in an ethanol solution of sodium ethoxide to obtain a raw material 4,6-dihydroxypyrimidine represented by a formula (VI); nitrifying the 4,6-dihydroxypyrimidine to obtain 4,6-dihydroxy-5-nitropyrimidine represented by a formula (V); carrying out chlorination reaction on the 4,6-dihydroxy-5-nitropyrimidine (V) to obtain 4,6-dichloro-5-nitropyrimidine represented by a formula (IV), carrying out aminolysis reaction on the 4,6-dichloro-5-nitropyrimidine (IV) and an saturated aminoethanol solution to obtain 4,6-diamino-5-nitropyrimidine represented by a formula (III); carrying out catalytic hydrogenation on the 4,6-diamino-5-nitropyrimidine (III), and reducing a nitro group to obtain 4,5,6-triaminopyrimidine represented by a formula (II); making the 4,5,6-triaminopyrimidine (II) react with ethyl orthoformate in acetic anhydride to obtain the adenine represented by the formula (I). The method provided by the invention has the advantages of cheap and easily-obtained raw materials, mild reaction conditions, single product, high total yield, low production cost and easiness in industrial production.

Description

technical field [0001] The invention relates to a chemical synthesis method of adenine, in particular to a novel chemical synthesis method of adenine. Background technique [0002] Adenine (Compound I), English name: Adenine, Chinese name: 6-aminopurine, CAS number: 73-24-5, molecular formula is C 5 h 5 N 5 . It is an important pharmaceutical raw material and intermediate. It is used for biochemical research and drug analysis such as the production of adenosine, ATP, ADP, new anti-AIDS drugs, vitamin B4 and plant growth hormone 6-benzyl adenine, and can prevent and treat leukopenia caused by various reasons. At the same time, it is also a component of nucleic acid, participates in the synthesis of RNA and DNA in organisms, and can promote white blood cell proliferation when white blood cells are lacking. It can also be used for blood storage, and other medical and biochemical research. [0003] The currently publicly reported synthetic routes mainly include the followi...

Claims

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Application Information

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IPC IPC(8): C07D473/34
Inventor 韩莹邓瑜袁宇张扬
Owner YANGZHOU UNIV
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