CN104098569B - A kind of purification process of medicinal folic acid - Google Patents

A kind of purification process of medicinal folic acid Download PDF

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CN104098569B
CN104098569B CN201410376142.8A CN201410376142A CN104098569B CN 104098569 B CN104098569 B CN 104098569B CN 201410376142 A CN201410376142 A CN 201410376142A CN 104098569 B CN104098569 B CN 104098569B
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folic acid
acid
heated
purified water
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CN104098569A (en
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张颖
刘真豪
刘鹏
郑良文
朱玉正
高国锐
王学斌
刘元鑫
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Jinan Kanghe Medical Technology Co., Ltd.
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JINAN KANGHE MEDICAL TECHNOLOGY Co Ltd
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D475/00Heterocyclic compounds containing pteridine ring systems
    • C07D475/02Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4
    • C07D475/04Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4 with a nitrogen atom directly attached in position 2

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Abstract

The invention provides a kind of purification process for medicinal folic acid, the systematic acid-base method that used of the method carries out purifying to folic acid crude product, preparation that can be repeated meets the folic acid finished product of standards of pharmacopoeia, its Folic Acid purity is more than 99%, and in the folic acid after refining, pteroic acid impurity content is below 0.1%. This method is refined for the more difficult pteroic acid impurity of removing in folic acid crude product, and its purification process is with low cost, easy and simple to handle, be easy to amplify; Purity and the production efficiency that can effectively improve on the other hand folic acid, be conducive to Application and Development in large-scale production.

Description

A kind of purification process of medicinal folic acid
Technical field
The invention belongs to compound preparation field, be specifically related to a kind of purification process of medicinal folic acid.
Technical background
Folic acid (folicacid) is a kind of B family vitamin being extensively present in green vegetable fruit. Nineteen forty-one, the people such as American scholar Mitchell have found this compound with anti-anaemia effect in spinach, because this compound mainly comes from plant leaf blade, so called after folic acid. 1945, the people such as Angier synthesized folic acid and have completed the mensuration of its structure.
Folic acid is called as Cobastab9Or Bc, its chemistry pteroylglutamic acid by name. In the structure of folic acid, comprise pteridine, p-aminobenzoic acid and glutamic acid structure. Folic acid finished product is a kind of orange-yellow crystal, is heated to 250 DEG C of decomposition. Folic acid is the necessary type organic matter in body normal activities process that sustains life, and after being absorbed, can participate in each process of vital movement by metabolism composition various active coenzyme by body. Its main application comprises: (a) participate in the synthetic of nucleic acid, promote division and the breeding of cell. (b) important component of formation hemoglobin. (c) conversion of promotion several amino acids. (d) supply with the important chemical substance that nerve endings generates and transmission is got excited.
The insufficiency of intake of folic acid can cause multiple corresponding deficiency disease, evidence suggests: the shortage of folic acid and neonate's deformity, macrocytic anemia and angiocardiopathy have significant correlation. The shortage of folic acid also has direct or indirect relation with various diseases such as senile dementia, parasitic disease, scurvy and rheumatoid arthritis. Current research also finds, folic acid also has suitable active anticancer, although anticancer mechanism is not clear, and being found to be us and further understanding, control of folic acid active anticancer, and then treatment cancer provides new method and approach. In recent years, medical research also finds, folic acid also has mitigation to schizophrenia, can treat atrophic gastritis, suppress bronchus squamous and transform, the diseases such as the coronary sclerosis that prevention and treatment cause because of homocysteine blood and cardiac damage, miocardial infarction.
The correlated product of folic acid and folic acid has been widely used in food, medicine, feed, scientific research and chemical industry. As far back as 1998, U.S. food and Drug Administration (FDA) just implemented the folic acid strengthening regulation for cereal products. British government or with within 2015, carry out folic acid fortified flour policy. China is also by iterative method " 7+1 " enriched nutritive flour, and folic acid is one of seven kinds of basic components wherein. According to incompletely statistics, in developing country, the related industry of folic acid and folic acid can relate to approximately 7%~9% GDP. The acquisition of folic acid at present mainly relies on chemical synthesis, and the common method of domestic production folic acid is now: N-NSC 71042, trichloroacetone and TAHMS are prepared folic acid crude product as intermediate. Folic acid is the valuable source that is related to national economy, and folic acid industrial expansion is also the important embodiment of a national strength.
At present, the total output of global folic acid is about 900-1000 ton; This wherein high-purity folic acid of 5% be medicinal folic acid. And the demand of medicinal folic acid also presents the situation of cumulative year after year. The method of folic acid purifying can be divided into salt refining method and the large class of acid treating method two.
Patent US2694710 and US2634271 have introduced respectively the method for purifying folic acid, and the sample that the purification process of above-mentioned patent Introduction obtains after testing, can not meet present pharmaceutical folic acid quality standard. And existing additive method, or be to realize industrialization, or purifying cost is higher, therefore, searches out a process for purification not only economical and practical but also easy and simple to handle and becomes very urgent.
Summary of the invention:
The present invention is directed to the refining technical deficiency of existing folic acid, a kind of purification process of medicinal folic acid is provided, it utilizes acid-base method to carry out purifying to folic acid crude product, and preparation that can be repeated meets the folic acid finished product of standards of pharmacopoeia; It is with low cost, easy and simple to handle, be easy to amplify; Purity and the production efficiency that can effectively improve on the other hand folic acid, be conducive to Application and Development in large-scale production.
The present invention realizes by the following technical solutions:
A purification process for medicinal folic acid, is characterized in that comprising the following steps:
(1) folic acid crude product is joined in purified water, be heated to 90~100 DEG C, add solid base in batches, regulate pH=11-13, treat that solid dissolves completely, add active carbon, be heated to seethe with excitement and keep micro-45min of boiling, filter while hot; Mother liquor slowly drips acid solution while hot, regulates pH=2.5-3.5, cooling stirring and crystallizing, suction filtration, dry;
(2) sulfuric acid solution of 30-50% is slowly joined in the folic acid of above-mentioned primary purification, control temperature 45-60 DEG C, stir, until solid dissolves completely, stir half an hour; Slowly drip purified water, temperature control 55-75 DEG C, strengthens stirring dynamics, and solid is separated out, cooling, and suction filtration, a small amount of ethanol is washed, dry;
(3) above-mentioned secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add solid base in batches, regulate pH=11-13, treat that solid dissolves completely, add active carbon, be heated to seethe with excitement and keep micro-45min of boiling, filter while hot; Mother liquor slowly drips acid solution while hot, regulates pH=2.5-3.5, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying, yield is 68-75%.
Preferably, in step (1) and (3), described solid base is NaOH or potassium hydroxide, and described acid solution is hydrochloric acid, sulfuric acid, phosphoric acid, nitric acid or the formic acid solution of 6-12M concentration; Preferred, described solid base is NaOH or potassium hydroxide, and described acid solution is the hydrochloric acid solution of 6M concentration.
Preferably, in step (2), described sulfuric acid solution concentration is 40%, 55 DEG C of acid adding control temperature, and adding water management temperature is 55-60 DEG C, mixing speed 600-750 rev/min.
Further preferred, the purification process of described medicinal folic acid, comprises the following steps:
(1) folic acid crude product is joined in purified water, be heated to 90~100 DEG C, add solid sodium hydroxide in batches, regulate pH=12.0, treat that solid dissolves completely, add the active carbon of mass ratio 5%, be heated to seethe with excitement and keep micro-45min of boiling, filter while hot; Mother liquor slowly drips the hydrochloric acid solution of 6M while hot, regulates pH=3.0, cooling stirring and crystallizing, and suction filtration is dry;
(2) 40% sulfuric acid solution is slowly joined in the folic acid of above-mentioned primary purification, control 55 DEG C of temperature, stir, until solid dissolves completely, stir half an hour; Slowly drip purified water, temperature control 55-60 DEG C, mixing speed is 750 revs/min, solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry;
(3) above-mentioned secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add NaOH in batches, regulate pH=12.0, treat that solid dissolves completely, add the active carbon of mass ratio 5%, be heated to the 45min that seethes with excitement, filter while hot; Mother liquor slowly drips 6M hydrochloric acid solution while hot, regulates pH=3.0, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying.
With respect to prior art, the invention has the beneficial effects as follows:
Major impurity in folic acid purge process and troublesome impurity are mainly pteroic acid. First the present invention uses alkali solution technique, the most of impurity in crude product and the higher impurity of content is removed, then impurity content is further reduced by acid-soluble method, and at this moment pteroic acid content can slightly increase, and finally re-uses alkali solution technique, and the content of pteroic acid is down to standards of pharmacopoeia. The systematic acid-base method that used of the present invention carries out purifying to folic acid crude product, and preparation that can be repeated meets the folic acid finished product of standards of pharmacopoeia, and its Folic Acid purity is more than 99%, and in the folic acid after refining, pteroic acid impurity content is below 0.1%. This method is for the more difficult pteroic acid impurity of removing in folic acid crude product, with low cost, easy and simple to handle, be easy to amplify, yield is high; Purity and the production efficiency that can effectively improve folic acid, be conducive to Application and Development in large-scale production.
Detailed description of the invention:
In order further to set forth technical scheme of the present invention, describe below in conjunction with embodiment. In the present embodiment, folic acid crude product is selected and is taked N-NSC 71042, trichloroacetone and TAHMS to come synthetic folic acid product, content >=90% of folic acid, pteroic acid content≤3.0% as intermediate. Should be noted that embodiment is to the further illustrating and explaining of summary of the invention, but not restriction to protection domain.
Embodiment 1
40% sulfuric acid solution 470ml is slowly joined to (pharmacopeia HPLC method detects, folic acid purity 91.1%, pteroic acid content 2.8%) in 50g folic acid crude product, control 55 DEG C of left and right of temperature, stir, until solid dissolves completely, stir half an hour. Slowly drip purified water 1.6L, temperature control≤60 DEG C, mixing speed is 750 revs/min, solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry. Highly finished product are joined in purified water, be heated to 90~100 DEG C, add NaOH 5.8g in batches, regulate pH=11.9 to treat that solid dissolves completely, add the active carbon of 2.5g, be heated to the 45min that seethes with excitement, filter while hot. Mother liquor slowly drips 6M hydrochloric acid solution while hot, regulates pH=2.9, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying. Yield is that 86%, HPLC detects folic acid purity 98.2%, pteroic acid 1.1%.
Embodiment 2
Folic acid crude product 50g(pharmacopeia HPLC method is detected, folic acid purity 91.1%, pteroic acid content 2.8%) join in purified water 1.5L, be heated to 90~100 DEG C, add solid sodium hydroxide 8.3g in batches, regulate pH=11.8, treat that solid dissolves completely, add 2.5g active carbon, be heated to the 45min that seethes with excitement, filter while hot. Mother liquor slowly drips while hotConcentrated hydrochloric acid solution, regulate pH=2.2, cooling stirring and crystallizing, suction filtration is dry. 40% sulfuric acid solution 450ml is slowly joined in the folic acid of primary purification, control 55 DEG C of left and right of temperature, stir, until solid dissolves completely, stir half an hour. Slowly drip purified water 1.5L, temperature control≤60 DEG C, mixing speed is 750 revs/min, solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry. Secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add NaOH 6.0g in batches, regulate pH=12.0, treat that solid dissolves completely, add the active carbon of 2.5g, be heated to the 45min that seethes with excitement, filter while hot. Mother liquor slowly drips concentrated hydrochloric acid solution while hot, regulates pH=2.1, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying. Yield is that 61%, HPLC detects folic acid purity 98.9%, pteroic acid 0.3%.
Embodiment 3
Folic acid crude product 50g(pharmacopeia HPLC method is detected, folic acid purity 91.1%, pteroic acid content 2.8%) join in 1.5L purified water, be heated to 90~100 DEG C, add solid sodium hydroxide 8.5g in batches, regulate pH=12.1, treat that solid dissolves completely, the active carbon that adds 2.5g, is heated to the 45min that seethes with excitement, and filters while hot. Mother liquor slowly drips the hydrochloric acid solution of 6M while hot, regulates pH=3.1, cooling stirring and crystallizing, and suction filtration is dry. Will50% sulfuric acid solution440ml slowly joins in the folic acid of primary purification, controls 55 DEG C of left and right of temperature, stirs, until solid dissolves completely, stirs half an hour. Slowly drip purified water 1.5L, temperature control≤60 DEG C, mixing speed is 750 revs/min, solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry. Secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add NaOH 5.8g in batches, regulate pH=12.2, treat that solid dissolves completely, add the active carbon of 2.5g, be heated to the 45min that seethes with excitement, filter while hot. Mother liquor slowly drips 6M hydrochloric acid solution while hot, regulates pH=3.0, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying. Yield is that 72%, HPLC detects folic acid purity 99.0%, pteroic acid 0.3%.
Embodiment 4
Folic acid crude product 50g(pharmacopeia HPLC method is detected, folic acid purity 91.1%, pteroic acid content 2.8%) join in 1.5L purified water, be heated to 90~100 DEG C, add solid sodium hydroxide 8.4g in batches, regulate pH=12.0, treat that solid dissolves completely, the active carbon that adds 2.6g, is heated to the 45min that seethes with excitement, and filters while hot. Mother liquor slowly drips the hydrochloric acid solution of 6M while hot, regulates pH=3.1, cooling stirring and crystallizing, and suction filtration is dry. Slow 40% sulfuric acid solution 460ml is joined in the folic acid of primary purification slowly, control 55 DEG C of left and right of temperature, stir, until solid dissolves completely, stir half an hour. Slowly drip purified water 1.5L,Temperature is 82-89 DEG C, mixing speed is 750 revs/min, solid is separated out, and cooling, suction filtration, a small amount of ethanol is washed, dry. Secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add NaOH 5.9g in batches, regulate pH=12.0, treat that solid dissolves completely, add the active carbon of 2.5g, be heated to the 45min that seethes with excitement, filter while hot. Mother liquor slowly drips 6M hydrochloric acid solution while hot, regulates pH=3.0, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying. Yield is that 68%, HPLC detects folic acid purity 98.5%, pteroic acid 1.0%.
Embodiment 5
Folic acid crude product 50g(pharmacopeia HPLC method is detected, folic acid purity 91.1%, pteroic acid content 2.8%) join in 1.6L purified water, be heated to 90~100 DEG C, add solid sodium hydroxide 8.2g in batches, regulate pH=12.0, treat that solid dissolves completely, the active carbon that adds 2.5g, is heated to the 45min that seethes with excitement, and filters while hot. Mother liquor slowly drips the hydrochloric acid solution of 6M while hot, regulates pH=3.1, cooling stirring and crystallizing, and suction filtration is dry. 40% sulfuric acid solution 465ml is slowly joined in the folic acid of primary purification, control 55 DEG C of left and right of temperature, stir, until solid dissolves completely, stir half an hour. Slowly drip purified water 1.5L, temperature control≤60 DEG C, mixing speed is 750 revs/min, solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry. Secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add NaOH 6.1g in batches, regulate pH=12.1, treat that solid dissolves completely, add the active carbon of 2.5g, be heated to the 45min that seethes with excitement, filter while hot. Mother liquor slowly drips 6M hydrochloric acid solution while hot, regulates pH=3.1, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying. Yield is that 75%, HPLC detects folic acid purity 99.4%, pteroic acid 0.1%.
Embodiment 6
Folic acid crude product 50g(pharmacopeia HPLC method is detected, folic acid purity 91.1%, pteroic acid content 2.8%) join in 1.5L purified water, be heated to 90~100 DEG C, add solid sodium hydroxide 8.1g in batches, regulate pH=11.8, treat that solid dissolves completely, the active carbon that adds 2.5g, is heated to the 45min that seethes with excitement, and filters while hot. Mother liquor slowly drips the hydrochloric acid solution of 6M while hot, regulates pH=3.2, cooling stirring and crystallizing, and suction filtration is dry. 40% sulfuric acid solution 457ml is slowly joined in the folic acid of primary purification, control 55 DEG C of left and right of temperature, stir, until solid dissolves completely, stir half an hour. Slowly drip purified water 1.5L, temperature control≤60 DEG C, mixing speed is 750 revs/min, solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry. Secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add NaOH 5.7g in batches, regulate pH=12.1, treat that solid dissolves completely, add the active carbon of 2.5g, be heated to the 45min that seethes with excitement, filter while hot. Mother liquor slowly drips 6M hydrochloric acid solution while hot, regulates pH=2.9, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying. Yield is that 71%, HPLC detects folic acid purity 99.5%, pteroic acid 0.1%.
Embodiment 7
Folic acid crude product 50g(HPLC official method is detected, folic acid purity 88.7%, pteroic acid content 3.0%) join in 1.6L purified water, be heated to 90~100 DEG C, add solid sodium hydroxide 8.2g in batches, regulate pH=11.7, treat that solid dissolves completely, the active carbon that adds 2.5g, is heated to the 45min that seethes with excitement, and filters while hot. Mother liquor slowly drips the hydrochloric acid solution of 6M while hot, regulates pH=3.1, cooling stirring and crystallizing, and suction filtration is dry. 40% sulfuric acid solution 451ml is slowly joined in the folic acid of primary purification, control 55 DEG C of left and right of temperature, stir, until solid dissolves completely, stir half an hour. Slowly drip purified water, temperature control≤60 DEG C, mixing speed is 750 revs/min, solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry. Secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add NaOH 5.5g in batches, regulate pH=12.2, treat that solid dissolves completely, add the active carbon of 2.6g, be heated to the 45min that seethes with excitement, filter while hot. Mother liquor slowly drips 6M hydrochloric acid solution while hot, regulates pH=3.0, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying. Yield is that 68%, HPLC detects folic acid purity 99.3%, pteroic acid 0.1%.
The Purifying Process of Folic Acid contrast test that embodiment 1 is prior art.
Embodiment 2-3 is the preferred contrast test of Purifying Process of Folic Acid acid concentration of the present invention, and wherein embodiment 2 is for adopting the contrast test of concentrated hydrochloric acid, and embodiment 3 is for adopting the contrast test of 50% sulfuric acid solution.
Embodiment 4 is the preferred contrast test of Purifying Process of Folic Acid temperature of the present invention, and the sulfuric acid solution that embodiment 4 is 40% slowly joins in the folic acid of above-mentioned primary purification, controls 55 DEG C of left and right of temperature, stirs, until solid dissolves completely, stirs half an hour; Slowly drip purified water, temperature control 82-89 DEG C, strengthens stirring dynamics, and solid is separated out, cooling, and suction filtration, a small amount of ethanol is washed, dry.
Embodiment 5-7 is the test of the optimal procedure parameters of Purifying Process of Folic Acid of the present invention.
Can be found out by above-described embodiment 2-7, in the present invention, the processing step of optimization, technological parameter be the concentration, the temperature control effect while dripping of concentration, the sulfuric acid of hydrochloric acid especially, very large to the relationship between quality of folic acid final finished. And use method of the present invention can repeatability the qualified folic acid finished product of preparation pharmacopeia.

Claims (4)

1. a purification process for medicinal folic acid, is characterized in that comprising the following steps:
(1) folic acid crude product is joined in purified water, be heated to 90~100 DEG C, add solid base in batches, regulate pH=11-13, treat that solid dissolves completely, add active carbon, be heated to seethe with excitement and keep micro-45min of boiling, filter while hot; Mother liquor slowly drips acid solution while hot, regulates pH=2.5-3.5, cooling stirring and crystallizing, suction filtration, dry;
(2) 40% sulfuric acid solution is slowly joined in the folic acid of above-mentioned primary purification, control 55 DEG C of temperature, stir, until solid dissolves completely, stir half an hour; Slowly drip purified water, temperature control 55-60 DEG C, strengthens stirring dynamics, mixing speed 600-750 rev/min, and solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry;
(3) above-mentioned secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add solid base in batches, regulate pH=11-13, treat that solid dissolves completely, add active carbon, be heated to seethe with excitement and keep micro-45min of boiling, filter while hot; Mother liquor slowly drips acid solution while hot, regulates pH=2.5-3.5, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying;
Described in step (1) and (3), solid base is NaOH or potassium hydroxide, and described acid solution is hydrochloric acid, sulfuric acid, phosphoric acid, nitric acid or the formic acid solution of 6-12M concentration.
2. the purification process of medicinal folic acid according to claim 1, is characterized in that: in step (1) and (3), adjust alkali pH=12, acid adjustment pH=3.0.
3. the purification process of medicinal folic acid according to claim 1, is characterized in that: in step (1) and (3), described solid base is preferably NaOH, and described acid solution is the hydrochloric acid solution of 6M concentration.
4. the purification process of medicinal folic acid according to claim 1, is characterized in that comprising the following steps:
(1) folic acid crude product is joined in purified water, be heated to 90~100 DEG C, add solid sodium hydroxide in batches, regulate pH=12.0, treat that solid dissolves completely, add the active carbon of mass ratio 5%, be heated to seethe with excitement and keep micro-45min of boiling, filter while hot; Mother liquor slowly drips the hydrochloric acid solution of 6M while hot, regulates pH=3.0, cooling stirring and crystallizing, and suction filtration is dry;
(2) 40% sulfuric acid solution is slowly joined in the folic acid of above-mentioned primary purification, control 55 DEG C of temperature, stir, until solid dissolves completely, stir half an hour; Slowly drip purified water, temperature control 55-60 DEG C, mixing speed is 750 revs/min, solid is separated out, cooling, suction filtration, a small amount of ethanol is washed, dry;
(3) above-mentioned secondary fine goods are joined in purified water, be heated to 90~100 DEG C, add NaOH in batches, regulate pH=12.0, treat that solid dissolves completely, add the active carbon of mass ratio 5%, be heated to the 45min that seethes with excitement, filter while hot; Mother liquor slowly drips 6M hydrochloric acid solution while hot, regulates pH=3.0, cooling stirring and crystallizing, and suction filtration, respectively with sodium bicarbonate solution, purified water and a small amount of ethanol washing, forced air drying.
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