• 专利附录
  • 专利说明
  • 权利要求
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    • 专利摘要:
    6-Fluoro-4-chromanone, a sorbinil intermediate, is regenerated from enantiomeric and mixtures of enantiomeric and racemic compounds obtained as major by-products in the synthesis of sorbinil. The regenerated intermediate is useful in the synthesis of additional sorbinil.
    公开号:SU1240358A3
    申请号:SU843757904
    申请日:1984-07-02
    公开日:1986-06-23
    发明作者:Венделл Кью Беркели (Младший)；Дитрих Хаммен Филип；Сарджент Массетт Стефен；Милдс Мур Бернард；Джон Сиско Роберт
    申请人:Пфайзер Инк (Фирма)；
    IPC主号:
    专利说明:

      I -
    This invention relates to a new method for regenerating purified 6-fluoro-4-chromenone, which it finds. application in the synthesis of sorbnyl as a starting product, which is used to prevent or. reducing the chronic complications of diabetes. .
    The purpose of the invention is a new method of regeneration of purified 6-ftop-4-xpo-ma1done, which allows the utilization of sorbinyl synthesis waste and, at the same time, increases the yield of sorbinyl.
    Limer 1. Sorbinyl through its (d) -3-aminomethylpinan salt.
    9.5 g (46.6 mol) of (-) - 3-aminomethyl-phenanhydride chloride, 186 ml of ethyl acetate and 93 ml of sodium hydroxide 1 and are subjected to intensive sleeping for 10 minutes. The organic layer is separated, washed with 93 ml of water, dried; over sulf-rym magnesium and extrude to obtain 75.5g of the 99% yield of (-) - 3-aminobhylpinan-free. bases in the form of butter; and - - -54.85 (c - TV in methanol), which is then dissolved in 20 ml of methanol. .. . .
    10.0 g (42, Cmmo) of racemic 6-fluorospiro 4H-1-benzopyran-4,4-im dazolin -2, 5-dione is dissolved in 214 MP of 2-propanol and 194 ml of methanol is boiled off. Under a reflux condenser, a solution of amine solution of amine is added to this solution, as a result of which a clear solution is obtained at reflux temperature (71 ° C). This solution is then slowly cooled (crystallization began at a temperature of 27 ° C) and subjected to stirring at room temperature for 6 hours. As a result, filtration and drying, in vacuum at 40 ° C, 6.81 g of solid (-X- 3-amino-methyl-pinane salt of sorbinyl with the melting point of 127.5-196 C (with decomposition) (d -8.2 ° (s -1, in methanol). The product yield from the stage is 79.6%.: Derived from it The mother liquor is evaporated to dryness to obtain crude (-) - 3-aminomethyl-pinane salt of sorbinyl enantiometer, the main contaminant being (-) - 3 amino amino methyl salt of sorbinyl.
    6.7 with sorbinyl CO. PI is dissolved at boiling point in
    240358.
    80.4 ml of a 1: 1 mixture of methanol with isopropanol is slowly cooled to room temperature and the resulting solid material is granulated for 2 hours. Purified. the salt was filtered off using 4 ml of a 1: 1 mixture of methanol and isopropanol for
    washes, then dried under vacuum at 40 ° C to obtain 4.42 g of product with a melting point of 119-208 ° C (with decomposition); oi +3.9 (s -1, V; methanol). Vyosod from the stage
    66%. . ......-.
    4.33 g (10.7 mmol) of purified salt is distributed between 107.5 ml of ethyl acetate and 53.8 ml of 1 n hydrochloric acid. The organic slab is separated, washed with 54 ml of 1N hydrochloric acid, 5 ml of water and -54 MP brine, dried over magnesium sulfate, filtered, evaporated in vacuo to give a suspension, washed with 3 portions, 50 ml of ethyl acetate to a final volume of 12 ml, granulated for 3 hours, filtered and dried under vacuum at 40 ° C to obtain 2.18 g of sorbinyl with a melting point of 234-242 °; s
    - + 51.2 (s -1, methanol) 4 Output from the stage 86.2%. Alternatively
    The dried organic layer is subjected to an extraction treatment with an equivalent amount of 1N sodium hydroxide solution. The extract is separated and freeze dried to obtain the sodium salt of sorbinyl, the first salt.
    The aqueous salts after the removal of the sorbene, binil are combined (226 ml) with 11.3 ml of dichloromethane and the pH value of the acid is adjusted to 10.0 by adding 25%
    sodium hydroxide. The aqueous layer is separated and subjected to an exection. Processing of 55 ml of a fresh portion of dichloromethane. The dichloromethane layers are combined, dried in vacuo to a residual volume of 60 ml, rinsed with 30 ml of water, dried over magnesium sulfate and embedded in a separation of 1.58 g of (-) - 3-aminomethylphenane as an oil-like product; oi -55,5 ° (s -1, methanol).
    Srrbinil is subjected to further purification by dissolving in 20 ml of hot ethanol, concentrated to half the volume and granulated for 4 hours at room temperature. Purified sorbinyl was filtered and dried at 40 ° C under vacuum.
    3
    obtaining 1.82 g of product with a melting point of 234-24-1.5 ° C; about +53.1. The output from the stage of 91%. Total yield 41.2%.
    By the same technology. Extraction crude. (-) - Z-aminomethylpinano-. Sorbinil enantiomer is converted to (-) - 3-aminomethylphenyl suitable for recycling, and sorbinyl enantiomer contaminated with racemate.
    EXAMPLE 2: 6-fluoro-4-chromanone from the sorbinyl enantiomer and racemate.
    100 g (0.432 mmol) of levravrakak tsego (R-) and / or racemic (PS-) - 6-fluorospir- (chroman-4,4-imidazolidine) -2, 5-dione are suspended in 750 MP of water. Then, 267.0 g (0.846 mol) of barium oxide octahydrate are added to the suspension and the liquid suspension formed is boiled under reflux for 48 hours. The thick suspension formed is cooled to 60-65 ° C and added 100 g (0.876 mol) of ammonium carbonate are put into it. Then the spam is stirred for 30 minutes and filtered at 50-55 C using 300 ml of warm water to wash in the collected inorganic salts. The combined filtrate and washing liquid is acidified with hydrochloric acid, bringing the pH from 8.5 to 4.5-5.0. In an acidified solution, 57.0 (0.427 mol) of N-chlorosuccinimide are added in separate portions over a period of 30-45 minute intervals. The resulting suspension is stirred for 17 hours at room temperature and then for 1 hour at 15 seconds. The resulting solid product is filtered, dissolved in dichloromethane, the solution is treated with activated carbon and dichloromethane is replaced with hexane to a boiling point of 68-69 s and a final volume of 400-500 ml, and crystallization occurs during this replacement. After cooling and leaching for 1 hour at 20-25 ° C, the purified target product was filtered by filtration, 50.2-g, the physical properties of the product being identical to the physical properties of the known material.
    The target product obtained in this way, as an impurity contains
    3584.
    6-fluoro-4-chloroiminochroman, which affects the further use of the product in the process of synthesis of additional sorbinil. Said impurity is removed (after conversion to the desired 6-fluoro 2 -chromanone).
    PRI me R 3. Purification of the crude 6-fluoro-4-chromanone by hydrogenation. Chromanone containing as
    impurities 5.0 g of 6-fluoro-4-chloroiminochromanone 0.25 g of 5% palladium on coal. (50% moisture) and 100 mp of a mixture of water and ethanol in a 1: 1 ratio are mixed and the mixture is subjected to hydrogenation under pressure. 45 psi, 3.16 kg / sq. Cm, 4 atm of hydrogen for 2 h, and after this period of time the thick-layer chromatographic
    silica gel analysis (using toluene: methyl ethyl ketone: acetic acid in a ratio of 5: 2: 1 as eluent) shows the absence of more highly mobile
    chloramine (Rf-0,8) in 6-fluoro-4-chro. manona (Rf-0.7). The reaction mixture was diluted with 100 ml of methanol (which caused complete dissolution of the solid material, in addition to the catalyst), the catalyst was removed by vacuum filtration on a layer of diatomaceous earth, and the filtrate was evaporated in vacuo to a residual volume of 50 ° C (in a water bath at 45 ° C) cool down
    granulated for 15 minutes and filtered to obtain 2.65 g of purified product with a melting point of 108-112 seconds, with the data of a thin layer analysis above. ,
    PRI me R 4.: K5-4-Amino-6-fluoro; chroman-4-carboxylic acid, 78 g (0.33 mol) K8-6-ft6rspiro (chroman4, 4-imidazolidine) -2, 5-dione and 208.3 g (0.66 MOJjb) hydrate oxide hydrate suspension .and bari in 585 ml of water are slowly heated to boiling point (for 3 hours) and boiled under reflux for about 16 hours. Then this suspension is cooled to 80 ° C and added in separate portions for 5 minutes. 78 g of powdered ammonium carbonate. Note moderate foaming. After stirring for 1.5 hours at 80 ° G, the mixture is cooled to 60 ° C and filtered through diatomaceous earth using two
    portions of 100 ml of hot water. The combined filtrate and industrial liquid. the bones are evaporated to a volume of 200 MP and set to stand for j overnight. Then 600 ml of 2-propanol are added and the mixture is stirred at 70 ° C to dissolve the precipitated solids. The hot solution is treated with activated carbon, filtered through diatomaceous earth and washed with a hot mixture of water with 2-propanol in a 1: 1 ratio. The combined filtrate and washings were evaporated to a residual volume of 200 #i and water was displaced by 3 portions per ml of fresh 2-propanol. The prepared thick suspension is diluted with 200 ml of additional 2-propanol, cooled to 5 ° C, granulated for 0.5 h, filtered and air-dried to obtain the title product example in an amount of 63.6 g (yield 91.2%)., The melting point of which is 25 25-53 s (with decomposition).
    ., Example 5. RS-6-Fluoro-ureidochroman-4-carboxylic acid.
    A. 21.1: g (0.1 mol) of RS-4-amino-6-fluorochroman-4-carboxylic acid is suspended in 250 ml of water. In separate portions, 16.2 g (0.2 mol) of KOCN are added over 2.5 minutes.
    After almost complete dissolution the mixture is stirred for 2.2 hours at 35, during which the pH of the mixture increased from 6.8 to 9.1 and the dissolution process was completed. AT
    19.0 mp of concentrated hydrochloric acid is added over 1 hour, maintaining the solution temperature in the range of 25–29 ° C. The resulting suspension is granulated for 1 hour at a pH of 3.2–3.5, filtered by using 150 ml of water for rinsing from the target product, which was then partially air-dried, after which it was dried in vacuo for 50 hours at 50-55 ° C to obtain 20.0 g of material (79% yield).
    B. Exodus nya imid az OLI n (47.2 g,
    0.2 mol) and 28 g (0.7 mol) of sodium hydroxide are mixed in 600 ml of water and held 55 at reflux temperature for 40 hours. The reaction mixture is cooled to 24 ° C and led
    The pH is lowered from .11.8 to 5.0 by the addition of 6N hydrochloric acid. When the pH value is below 8, the occurrence of gas is noted. After stirring the suspension for 20 minutes at a pH of 5 for 32 minutes, 32.5 g (0.4 mol) of KOCN was added to it, the mixture was stirred for another 20 hours, and a small amount of water was washed through filtering with 50 ml of water for washing. amount of solid material. The value of the .pH of the combined filtrate and the washer fluid was adjusted from 8.5 to 4.0 by the addition of 6 ns of SOLIC acid. The precipitated product is filtered, washed with warm water and air dried to give 39.7 g (78% yield) of the substance, the melting point of which is 199 ° C (with decomposition).
    The hydrolysis step using sodium hydroxide is carried out at 11.8 ° C and an overpressure of 27 psig, 1.9 atm for 18 hours. As a result of the subsequent reaction with KOCN and separation, 38.8 g of the desired product are obtained ( yield 76.4%) with a melting point of 199-200 s (with decomposition). . . Instead of hydroxide, sodium, 26.4 g (0.4 mol) of 85% potassium hydroxide are used and reflux is held for 22 hours. As a result of reaction with KOCN and separation, 36 are obtained in the same manner as above. , 8 g (yield 72.4%) of the desired product with a melting point of 198-199 0 (with decomposition).
    Example 6. D - (+) - (1-Phenethyl) - ammonium-3-6-fluoro-4-ureidochroman-4-carboxylate. .
    10.0 g (39.4 mol) of E8-6-fluoro-4-ureidochroman-4-carboxylic acid are suspended in 400 ml of methanol at 45 + 5 ° C for 1 hour. For 4 minutes, the resulting liquid suspension is added are 4.87 g (40.1 mol) D - (+) -. (1-phenethyl) amine in 45 mp of methanol, resulting in a solution. The bath is then removed, the mixture is slowly cooled to room temperature, it is granulated for 16 hours and the crude target product is isolated by filtration, after which it is dried in air to obtain 6.4 g (yield 86.6%) of the substance with a temperature of
    melting point 206-210 ° C + 54.3 ° (s - 0.3 methanol). 6 g of the desired product are suspended in 180 ml of methanol at 4 ~ -5 ° C for 1 h,
    . Suspend suspension to room temperature, granulate for 3 hours. filtered and dried in air, as a result of which 4.4 g of purified target product is obtained, with a melting point of 214-216 ° s + 69 ° D
     (s - 0.3 methanol), -degree of recuperator-- give 73.3%, total yield 63.5%.
    The mother solution of the syphonic target product is extruded to obtain a mixture containing D - (+) - (} - enethyl) -ammonium-E-6-fluoro-4-ureidochroman-4-carboxylic acid. xylate together with the target product 8.3 g, melting point 198-200 sec ss -35.4 ° (s - 0.5 methanol), 20 acceptable for return to 6-fluoropa-4-x-mode. In one version this
     the mixture is distributed between ethyl acetate and water, initially bringing the pH to -10. The ethyl acetate layer is separated by 25 and the optically active amine recoids,. Reveal evaporated. Then the pH value of the aqueous phase is adjusted to 1-2 by addition of hydrochloric acid and subjected to extraction with fresh portions of ethyl acetate. The organic phase is washed with additional small portions of water, dried over magnesium sulfate and evaporated to obtain a mixture of R- and K8-6-fluoro-4-ureidochroman-5 4-carboxylic acid.
    , Example 7. Sorbinyl. P - (+) - (1- -phenethyl) - ammonium-8-fluoro-4-ureidochroman-4-carboxylate (4.3 g, 11 mol) is suspended in 30 ml of glacial acetic acid for a period of 2 hours, and a solution is formed after the first 15 minutes. Next, the solution is cooled to 60 ° C and evaporated to a residual volume of 10 MP. 21.5 Ml of water is added to the residue, heated to, as a result, the pY value of the resulting suspension is 3.5. After 5 minutes, the pH is adjusted to 4.5 by adding 4 mp of 4N sodium hydroxide (temperature is 28 ° C) and the mixture is cooled to 20 ° C over 30 minutes. Filtration is obtained by filtration. 2.35 g (yield 90.3%) of relatively pure sorbininyl with a melting point of 238-241 CM (s = 1, methanol). This sorbinol is purified by dissolving 2.2 g of the product in c. 27.4 ml of boiling acetone, which will be molded by hot filtration and evaporated. . residual volume of 3 mp. Formed slurry twice slowly diluted with 17.2 MP of hexane and evaporated to; a residual volume of 13 ml. As a result of filtration and air drying, 1.924 g (yield: 87.5%) is obtained. purified sorbinil with a temperature of: melting of 239.5-242.5 ° C, +54.5. (s - 1, methanol).
    56.2 g of relatively pure. Sorbinil with a melting point of 237-, (+52.3 (s-1, methanol), obtained in a similar way with a yield of 89.8% from) - (+) - 1- (phenethyl) ammonium- 8-6-fluoro-4-ureidochromanone-4-carboxes1 is dissolved in 700 mp of boiling acetone, the solution is clarified by filtration and evaporated to a residual volume of 300 mp. 400 ml of hexane is gradually added to this residue and the mixture is again evaporated to. residual volume of 300 MP. The steps of adding hexane and subsequent evaporation are repeated, and as a result, after vacuum drying, for 18 h, 54.9 g (HL 97.7%) of the desired product are obtained with a melting point of 236 g 241 C, 53.4 ° (from - 1, methanol) -.
    PRI me R 8. b - (-) - Ephedrine salt 5-6-fluoro-4-ureidochroman-4-carboxylic acid.
    A. 36.6 g (0.14 mol) of b-fluoro-4-chroman It is suspended in 1.07 L of acetone, the suspension is stirred at reflux temperature for 30 minutes and cooled to. In one portion, 24.4 g (0.148 mol) of (L -) - ephedrine is added to it. The slurry becomes thinner and almost a solution is formed. After less than 2 minutes
    when rapid crystallization begins. The suspension is then boiled under reflux for 2 hours, cooled to 40 ° C and filtered off by filtration. sugar-like crystals 6.1 g of the desired product with a melting point of 204 ° C (with decomposition- eM) +37.0 (s-1, methanol).
    At room temperature, a second solution is obtained from the matrix solution, 1Ch, t, 3 g of solid material with a temperature of nnsBJjeHHH 180-185 0 (with decomposition); {oQ O (s-1, methanol).
    As a result of the concentration of the mother liquor, 32.9 g of 5 foam-like solid material with a melting temperature of 72-90 ° C (with decomposition) and -55, (s -1, nol) are obtained.
    The first portion of solid material 10 (25 g) is re-suspended in 250 ml of boiling acetone (under reflux) and after cooling to a temperature, 24 g of product are obtained with a melting point of 205 ° C (decomposition) +38.2 (s - 1, methanol). As a result of evaporation of the mother liquor to dryness, 1.2 g of product are obtained with the melting point of EO-IO C (with decomposition); M 20 +34.4 (s - 1, methanol).
    Once suspended, 13 g of solid material is resuspended in 260 ml of acetone boiling under reflux, after which 25 the suspension is cooled to -temperature and 11.7 g of product is removed; ot +39.3 (s - 1, methanol). As a result of incorporation of the mother liquor, an additional 1.1 g of 30 solid material is obtained.
    B. 6-Fluoro-4-chromanone (100 g) is stirred at reflux temperature (65 ° C) in 374 ml of methanol for 30 mc,. after which the mixture is cooled to a temperature of 59 ° C. Then 7.42 ml of water and 68 g of L - (-) - ephedrine are added, as a result of which a rapid precipitate occurs. The suspension is boiled under reflux (). During 45 minutes it is cooled to 27 ° C and as a result of filtration 70.4 g of high-purity target pro- is directly separated. Duct, Mr +44.36 (s - 1.04 in metro-45 nol). The filtrate is evaporated to obtain crude diastereomeric salt, L (-) - ephedrine-K-6-fluoro-4-ureidochromal-4-carboxylate, 116.3 g.
    PRI m e. R- and RS-6 -fluoro-4- ° ureidochroman-4-carboxylic acid.
    A. Recovered B - (+) - (1-phenethyl) -ammonium-K-6-fluoro-4-ureidochroman-4-carboxeshgat (32.3 g), containing also a small amount of corresponding trunk 55 -ammonium B-carboxylate salt, mixed with 215 ml of 1N hydrochloric acid and stirred at 16-23 ° C
    within 21 hours. The desired product was filtered by filtration to obtain; 20.6 g (94% yield) of a substance with a melting point of 195-198 ° C (with decomposition).
    B. A column containing 50 ml of the previously used ion exchange resin (Amberlite, 1 RA 900) is slowly washed successively with 250 np of demineralized water, 250 ml of 1N sodium oxide hydrate, 250 ml of nitrogen purged water, and 250 ml of methanol purged with nitrogen. 10 g of the crude enantiomeric salt is then placed in this 50 ml of methanol, eluted with an additional 100 ml of methanol and the eluate is evaporated in vacuo to give 0.0109 mol of ephedrine given as determined by titrometric testing using a 0.1 N solution of hydrogen chloride in methanol. Then the column is eluted with 150 ml of methanol containing 4.4 g of dry hydrogen chloride and finally 150 ml of fresh methanol. These latter eluates in methanol containing hydrogen chloride and simply in methanol are combined and evaporated in vacuo to give 5.86 g of enantiomeric (R) and racemic (K5) -6-fluoro-4-ureidochroman-4-carboxylic acid .
    Example 10. Crude b-fluoro-4-chromanone from R and RS-6-fluor-4-ypeido-chroman-4-carboxylic acid.
    100 g of R and KZ-6-fluoro-4-ureidochroman-4-car & ampic acid are suspended in 475 ml of water. 32 g of a 50% hydrate of oxy is added to the suspension. sodium, resulting in incomplete dissolution. This mixture was kept for 40 minutes at boiling point XI00 ° C under reflux), due to which complete dissolution was achieved. The reflux was continued for 18 hours and then the mixture was cooled. PH value 9.6; thin layer chromatographic analysis showed incomplete reaction. The pH is raised to 12.0 by the addition of 13.8 g of a 50% sodium hydroxide solution and the mixture is again kept. boiling at reflux for 2.5 hours; after this period of time a thin layer chromatographic analysis on silica gel (a mixture of toluene
    with methyl ethyl ketone and acetic acid in the ratio of 5: 2: G as eluent) showed the presence of only traces of the starting material Rf-0.5 with a high concentration of the intermediate product, R and K5-6-fluoro-4-aminochroman-4-carboxylic acids (Rf - 0,0). The reaction mixture is cooled to 20 ° C and, while maintaining the temperature. At a level below 30 ° C, the pH is adjusted to 4.5 by adding concentrated hydrochloric acid to isolate the precipitate. Within 15 minutes, 53 g of N-chlorosuccinamide is added, maintaining the temperature below 30 ° C and a pH in the range of 4.0-4.5 simultaneously until 50 ml of 50% sodium hydroxide solution is added up to 7 ml. Reaction mixture stirred for 1 hour at a temperature of 25 seconds; moreover, during this period of time, the pH value was 5.2, and .bn-layer chromatographic analysis (in the described system) showed the complete don version of the intermediate amino acid into products. The pH is then adjusted to 9.6 by adding approximately 27 ml of 50% hydroxide oxide solution and sodium, the alkalized suspension is granulated for 2 hours at 20 seconds and the target product filtered by filtration (50.0 g) ; its melting point is 55-58 s (partial melting) and 65-73 s (complete melting, but the melt was not transparent); thin-layer chromatographic analysis (the above system). showed the presence of the target product (Rf - 0.7), containing about 6-. fluorine-4-chloriminochroman (Rf - 0.8).
    In the implementation of the proposed method, B - (+) - (1-phenethyl) ammonium-R- & -top-4-yreidoxy-4-carboxylate containing a small amount of corresponding D-ammonium is used. niy-3 to rboxylate. At the beginning. The stages of the process distribute the salt between a 50% sodium hydroxide solution and an equal volume of dichloromethane. The aqueous phase is carried out in 2 portions of 1/3 volume of dichloromethane. The organic layers were combined and evaporated to give 1) - (+) - (1-fethioyl) -amine acceptable for recycling. Waterway
    phase is passed through the rest STANDARD Order 3416/60 Circulation 379
    Produced gp. pr-tie, Uzhgorod, st. Project, 4
    , y 15 20 25 h
    ., -
    five
    din this method to obtain the target product.
    EXAMPLE 11. 6-Fluoro-4-chloroiminochroman from R and RS-6-fluoro-4-.yreidochroman.
    The experiment is repeated using
    one tenth of the quantities of the previous example, resulting in an intermediate R and RS-6-fluoro-4-aminochroman-4-carboxylic acid in sodium hydroxide solution. To this solution was added dropwise 48.2 ml of 15% solution of sodium chloride-chlorite, which is maintained in the range of 20–3 (fc. This mixture is stirred for 3.5 hours at 20–25 ° C; and During this period, thin-layer chromatographic analysis (the system is similar to that described in the previous example) showed the conversion of the amino acid to a practically pure target product, with insignificant traces of 6-fluoro-4-xp6manon. The desired product was filtered by filtration (3.8 g). Rf 0.8 systems.
    Example 12. 6-Fluoro-4-chronan from hlorin. . :
    3.6 g of 6-fluoro-4-chloroiminochroman and O, 18. g (in terms of dry weight) are 5% charged on coal at 50% moisture mixed with each other, in 72 MP mix of methanol with water in - 9: 1 wearing. The pH is adjusted to 2.0 by the addition of concentrated hydrochloric acid and the mixture is subjected to hydrogenation under spraying pressure of 40-50 psi, 2.8 - 3.2 kg / sq. Cm (3.7-4 atm) of hydrogen for 2 hours The catalyst was filtered through a bed of diatomaceous earth. A thin-layer chromatographic analysis of the filtrate (Rf - 0.7 in the system described in the precursors. Pax) showed that it contained only the desired product, easily evaporated in vacuo. Yield 90%. Thin-layer chromatographic analysis showed that a certain amount of product was retained on the filter cake from the catalyst, and this amount can be easily added to the suspension of the catalytic filter cake in methanol, then the target product is quantified in quantitative yield.
    Podyisnoe
    权利要求:
    Claims (1)
    [1]
    METHOD FOR GENERATION OF PURIFIED 6-ФТ0Р-4-ХР0МАН0НА, characterized in that the waste from the synthesis of sorbinyl is R or a mixture of R- and IZ-ft <erspiro (chroman-4,4-imidazolidine) —2,5-dione, or R- or a mixture of R- and KB-b-fluoro-4-ureidochroman
    4-carboxylic acid or its cationic salt is hydrolyzed in the presence of inorganic water. base when boiling, followed by acidification of the reaction medium to a pH of 4.5-5.0, the resulting R-or a mixture of R- and E5-amino-6-fluoro-chroman-4-carboxylic acid is destroyed by the action of a chlorinating agent in the presence of water, and the resulting mixture 6-fluoro-4-chromanone and b-fluoro-4-chlorimi-. Nochromanone is subjected to hydrogenation in an aqueous-organic medium over a noble metal catalyst under a pressure of 2.8-3.2 kg / cm 2 .
    SU number , „, 1240358 AZ
    1240358 2
    80.4 ml of a mixture of methanol with isopropanol in a ratio of 1: 1, slowly cooled to room temperature and the resulting solid material was granulated for 2 hours Purified. the salt is isolated by filtration using 4 ml of a mixture of methanol with Isopropanol in a ratio of 1: 1 for washing, after which it is dried in vacuum at 40 ° C to obtain "4.4'2 g of product with a melting point of 119208 ° C (with decomposition); [kJ = +3.9 β (s -1, in methanol). Exit from stage ι
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    HU191160B|1987-01-28|
    HK99587A|1987-12-31|
    CA1181754A|1985-01-29|
    IE832620L|1984-05-10|
    HUT36110A|1985-08-28|
    EP0111387A1|1984-06-20|
    PL142777B1|1987-11-30|
    US4431828A|1984-02-14|
    BG45387A3|1989-05-15|
    PH18265A|1985-05-14|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US4130714A|1977-05-23|1978-12-19|Pfizer Inc.|Hydantoin therapeutic agents|
    US4286098A|1980-03-28|1981-08-25|Pfizer Inc.|Process for the preparation of chiral hydantoins|US4620019A|1984-08-23|1986-10-28|Pfizer Inc.|S-6-fluoro-4-aminochroman-4-carboxylic acid derivatives useful as intermediates for sorbinil|
    US4551542A|1984-09-26|1985-11-05|Pfizer Inc.|Regeneration of 6-fluoro-4-chromanone from 6-fluoro-4-ureidochroman-4-carboxylic acid|
    US5340829A|1984-11-20|1994-08-23|Washington Research Foundation|Immunoregulatory agents|
    US4966911A|1984-11-20|1990-10-30|Washington Research Foundation|Immunoregulatory agents|
    US4841079A|1987-08-07|1989-06-20|Pfizer, Inc.|Process for the production of asymmetric hydantoins|
    US8579985B2|2006-12-07|2013-11-12|Ihip Surgical, Llc|Method and apparatus for hip replacement|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US06/440,657|US4431828A|1982-11-10|1982-11-10|Regeneration of 6-fluoro-4-chromanone from by-products in the synthesis of sorbinil|
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