• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The invention provides a novel method for producing phenylglycyl chloride hydrochlorides involving reaction of N-substituted phenylglycines with for example thionyl chloride and then gaseous hydrogen chloride, as well as certain novel starting materials for use in this process and certain end-products thereby produced.
    公开号:SU1205760A3
    申请号:SU802912501
    申请日:1980-04-25
    公开日:1986-01-15
    发明作者:Ашер Герд；Ридль Курт
    申请人:Биохеми Гмбх (Фирма)；
    IPC主号:
    专利说明:

    I
    The invention relates to an improved method for the preparation of phenylglydine derivatives of the general formula
    ABOUT
    CH-C-C
    H7.-HC1
    where P is hydrogen gTOM or hydroxy,
    used as intermediates in the preparation of derivatives of antibiotics.
    The aim of the invention is to simplify the process.
    The invention is illustrated by the following examples.
    Example 1. D - (-) - 4-hydroxyphenylglycyl chloride hydrochloride 5 hemisolvate dioxane,
    25 g of D - (-) - N-isopropoxycarbonyl-4-hydroxyphenylglycine are suspended in 250 ml of methylene chloride and 16 g of trichloroacetic acid are added to the mixture. While stirring and cooling on ice, 16 ml of thionyl chloride are added, after 10 minutes the mixture is heated to room temperature and stirred for 2-3 hours, after which the starting material is already absent according to those. After evaporation of the solvent, the residue is mixed with 300 ml of ethyl acetate and the solution is extracted once with 150 ml of water and then 100 ml of saturated brine. After drying with magnesium sulfate, the mixture is evaporated and the residue is mixed with 160 ml of dry dioxane and 80 ml of toluene. Gaseous HCV is introduced into the mixture, cooled with ice until complete crushing. After seeding with crystals and stirring at room temperature, crystallization soon begins. After stirring overnight, the crystals of the title compound are filtered and IR spectra are taken. Yield 28%.
    Example 2. D - (-) - phenylglycyl chloride hydrochloride, hemisolvate dioxane.
    According to the procedure of Example 1, 2.5 g of D - (-) - - isopropoxyphenylglycine, 25 ml of methylene chloride, 0.8 g of trichloro acetic acid and 1.2 ml of chloris 1207602 are introduced into the reaction.
    that thionyl. After 3 h, the mixture is cooled, 5 ml of dioxane are added and gaseous HC1 is passed through the mixture to g (most of them).
    g After the introduction of seed crystals, the mixture is stirred at room temperature for several hours, 5 and then the final product is removed. Yield 60%.
    Q Example 3. D - (-) - 4-hydroxyphenylglycyl hydrochloride, hemisolvate dioxane.
    2.5 g of D - (-) - H-isopropoxycarbonyl-4-hydroxyphenylglycine, 0.8 g of chloroacetic acid and 25 ml of L-hexane are mixed, cooling the reactants with ice .. with 1, 2 ml of thionyl chloride and the mixture - boil t for 1 h. The mixture is evaporated on a rotary actuator, the residue is mixed with 16 ml of dioxane and 8 ml of toluene. After saturation with gaseous NSB (carried out with cooling), introducing seed and stirring for several hours at room temperature, the product is filtered, washed with a mixture of dioxane - toluene (1: 1), then with a small amount of methylene chloride and dried. The product is identified by IR spectra and the formation of methylate (TLC). Yield 27%.
    Example 4, D - (-) - 4-hydroxyphenylglycyl chloride hydrochloride (hemisolvate dioxane).
    12.5 g of D - (-) - M-isopropoxycarbonyl-4-hydroxyphenylglycine are suspended in methylene chloride and 4 g of trichloroacetic acid and 8 ml of thionyl chloride are added. The mixture was boiled gently for 5 hours with stirring without access of moisture, and then cooled to 5 ° C. 25 ml of dioxane was added and gaseous HCf was passed through for 30 minutes. After the introduction of the seed mixture is stirred
     at room temperature until crystallization begins. After that, gaseous HC8 was bubbled through the mixture for 6 hours. The whole product is filtered under inert atmosphere.
     gas, rinse with a small amount of methylene chloride and dried over PjO. The yield is 78%.
    Example 5. D - (-) - 4-oxyfensh1- glycyl chloride hydrochloride,
    55 (hemisolvate dioxane).
    2 ,, 25 g D - (-) - M-methoxycarbonsch: - 4-hydroxyphenylglycine is dissolved in 20 ml of dioxane and 0.02 g is added
    thirty
    3
    trichloroacetic acid. After a solution of 0.8 ml of thionyl chloride in 5 ml of dioxane was added dropwise to the mixture, it was stirred, protected from moisture for 4 hours at. The mixture is then stirred with 8 ml of toluene, cooled to approximately O ° C, and gaseous HCB is passed through for 1 hour. The cooling agents are removed and, after seeding, the mixture is stirred for several hours at room temperature. The precipitate is filtered off, washed with methylene chloride and dried. Yield 27%
    PRI me R 6. D - (-) - D-hydroxyphenyl-glycyl chloride hydrochloride, (hemisolvate dioxane).
    2.25 g of D - (-) - N-methoxycarbonyl-4-hydroxyphenylglycine are suspended in 25 ml of methylene chloride, 0.8 ml of trichloroacetic acid is added, and then, with stirring, 1.4 ml are added dropwise at room temperature. thionyl chloride. The mixture is slowly boiled under stirring and removing moisture for 4-5 hours. The mixture is cooled, mixed with 7 ml of dioxane, and then hydrogen chloride gas is flushed for 30 minutes. After seeding, the mixture is stirred at 20–25 ° C until crystallization begins. After this, a weak stream of gaseous gas is bubbled in for several hours, the product is filtered off, protected from moisture, washed with methylene chloride and dried in a desiccator over silica gel. Yield 52%.
    Example 7. D - (-) - 4-hydroxyphenyl glycyl chloride, hydrochloric, (hemisolvate dioxane).
    2.4 g of D - (-) - M-ethoxycarbonyl-4-hydroxyphenylglycine is treated as described in Example 6, except that 1.6 g of trichloroacetic acid are used instead of 0.8 g. The yield is 30%.
    PRI me R 8. D - (-) - 4-hydroxyphenyl-glycyl chloride hydrochloride (hemisolvate dioxane).
    2.7 g of D - (-) - t-butoxycarbonyl-4-hydroxyphenylglycine are treated under the conditions described in Example 6. Yield 70%.
    Example 9. D - (-) - 4-hydroxyphenyl glycyl chloride hydrochloride (hemisolvate dioxane).
    057o
    3 g of D-wasp-benzyloxycarbonylamino. -4-hydroxy-acetic acid are dissolved in 20 ml of dioxane, 0.05 g of trichloroacetic acid is added and
    5 0.8 ml of thionyl chloride, the temperature of the mixture is maintained at 50 ° C for 1 h without access of moisture with stirring on a magnetic stirrer. After adding 8 ml of toluene mixture
    10 is cooled to -5 and for 1 h, gaseous HC2 is passed through it. After seeding, the mixture is stirred for 4 hours at room temperature, after which the desired product precipitates. It is filtered and dried in a vacuum desiccator over silica gel. Yield 56%.
    Example 10: D - (-) - 4-hydroxyphenyl hydrochloride nilglycyl chloride.
    To a solution of 12.5 g of D - (-) - N-isopropoxycarbonyl-4-hydroxyphenylglycine in 125 ml of methylene chloride and 8 g of trichloroacetic acid, is added 8 ml of thionyl chloride. The process is carried out at 40 ° C for 3 hours. The mixture is cooled with ice water, 100 ml of diisopropyl ether are added and the mixture is passed through .JQ for about 1.5 hours through gaseous HCP. After stirring at room temperature overnight, a well crystallized, non-solvated product is formed. Yield 80%.
    Example 11. D - (-) - 4-hydroxyphenylglycyl chloride hydrochloride.
    The mixture obtained after reacting thionyl chloride with D - (-) - N - isopropoxycarbonyl-4-hydroxyphenylglycine, described in Example 10, is mixed with 100 ML of di-n-butyl ether and the desired product is obtained by passing a mixture of HCB through a mixture. Yield 81%.
    Example 12. D - (-) - 4-hydroxyphenylglycyl chloride hydrochloride. Under the conditions described in Example 10, but using instead of 100 mc diisopropyl ether or 75 ml of anisole, 50 ml of tetrahydrofuran or 75 ml
    50 diethyl ether, receive the specified connection. Yield,%: anisole 47, tetrahydrofuran 72, diethyl ether 83.
    Example 13. D - (-) - 4-hydroxyne 55 nilglycyl chloride hydrochloride.
    A mixture of 38 g of p-toluenesulfonic acid, 125 ml of methylene chloride and 15 ml of thionyl chloride.
    40
    45
    and dpt for 1-1.5 hours. Add g of D - (-) - M-nsopropoxycarbonyl-α-oxyphenylglycine and 30 ml of tononyl chloride, and the mixture is gently boiled for 2 hours. After the addition. 200 ml of dry butyl acetate are cooled with gaseous NSO, and then the mixture is stirred for 1 hour while gaseous HC is passed through again (30 minutes). After an additional 30 minutes of stirring at 15 ° C. Adding 400-500 ml of dry methylene chloride, the mixture is stirred for 15 hours at room temperature and the reaction product is filtered off, protected from elagi. After washing with methylene chloride, the products are dried at room temperature in a vacuum desiccator. Yield 85%, Example 14. D - (-) - 4-hydroxyphenylglycyl chloride hydrochloride (hemisolvate dioxane), 190 g) -toluene sulfonic acid (water in 625 ml of methylene chloride is stirred for a short period of time with 119 g of thionyl chloride. 253 g of D - (-) - N-isopropoxycarbonyl-4-hydroxyphenylglycinyl and 238 g of thionyl chloride are added, the mixture is boiled for 2.5-3-h, after which a clear solution is formed after a short period of time. The mixture is cooled to C, and after adding 500 ml of dioxane, about 170 g of gaseous HC is introduced into the mixture, cooling it until the HC content is 100 mg / ml. The mixture is finally stirred for 10 hours at room temperature, the precipitated product is filtered off, washed with a mixture of dioxane - methipene chloride (1: 1) and methylene chloride and dried 24 hours under vacuum. 86% yield.
    Identification of D - (- 1-4-hydroxyphenyl-glycyl chloride hydrochloride (hemisolvate dioxane):
     (, her).
    Solvent content (gx): dioxane 16%; CILC6 0.2%. IR spectra, cm: 3280 (5), 1770 (S); 1735 (S), 1210 (5), 1170 (5), 865 (S).
    Identification of the unsolvated, crystalline D - (-) - oxyphenylphenylporide hydrochloride:
    c, j -ii2 ° (, her)
    0
    five
    0
    five
    0
    five
    0
    five
    Solvent content (tx); butyl acetate Oj 5%; 0.2%. Absorption bands of IR spectra, cm: 3000 (Vg); 1735 (S) -, 1170 (5); ZZS.
    The melting point was not determined by JJ due to decomposition.
    The examples below illustrate the preparation of the starting compounds of the compound;
    a) D - (-) - M-isopropoxycarbonyl - 4-hydroxyphenylglycine „
    1) 40 g of D - () - 4-hydroxyphenylglycine are suspended in 320 ml of water and mixed with a solution of 9.6 g of sodium hydroxide in 80 ml of water at room temperature. A clear solution is formed with a pH of 9.7. At the same time, two other solutions are prepared: 9.9 g of sodium hydroxide in 80 ml of water and 29.2 ml of isopropyl chloroformate in 50 ml of acetone, are added dropwise so that the pH remains in the range of 9.5 to 9.7 and the temperature is not exceeds more than 25 ° C. The mixture is stirred for 2 hours at room temperature. The final pH value is 9.6. The acetone is evaporated and the aqueous solution is extracted once with 50 ml of ether, acidified with hydrochloric acid (1: 1) and the acylation product is extracted three times with ethyl acetate, the total amount is 250 ml. The purified extracts are dried and the ethyl acetate is evaporated as fully as possible. The residue is mixed with chloroform, dissolved in it with heating, and the mixture is evaporated to more completely remove ethyl acetate. The residue is mixed with 150 ml of chloroform, re-heated, and the crystallization process is completed by adding 60 ml of hexane. After drying, the melting point of the product is 163-164 ° C.
    2, the procedure described in example 1a is repeated until the acetone is evaporated. The resulting solution is filtered, mixed with 40 ml of concentrated ammonia or an appropriate amount of sodium hydroxide and left to stand at room temperature for 1-2 hours. Then the mixture is acidified with hydrochloric acid (1: 1) with cooling and slow stirring until pH 1, 5-2 and the appearance of turbidity. Stirring is continued until the crystallization process is complete. The product is identified by titration and IR spectroscopy.
    3. 500 g of D - (.-) - 4-hydroxyphenylglycine is suspended in 4 l of water, the suspension is cooled to 2-5 ° C and a solution of 360 g of sodium hydroxide in 1 l of water is slowly added dropwise. The temperature is maintained below ori. Then, 900 ml of isopropyl chloroformate are added and the temperature is kept at 5 ° C. The mixture is stirred for 1 hour in an ice bath, and then 780 ml of 10 N, NaOH is added. After 30 minutes the mixture was filtered, the filtrate was acidified with sulfuric acid until it became turbid. After 5–10 min from the beginning of the crystalline process, some more sulfuric acid is added with stirring to pH 2.0. To complete the crystallization, the mixture is stirred for 15 ° Z. my, cooling it on ice. The mixture is washed with water and dried under vacuum, first at 50 ° C :, and then at YO-90 C. The compound obtained in this way is pure according to TLC data, and so on. 162-164 ° C and the specific angle of rotation (in methanol).
    b) D - (-) - M-methoxycarbonyl-4-oxiphenylglycine.
    40 g of D - (-) - 4-hydroxyphenylglycine in 320 ml of water are mixed with a solution of 9.6 g of NaOH in 80 ml of water. To it is added a mixture of 9.6 g of NaOH in 80 ml of water and 19.8 ml of methyl chloroformate in 40 ml of acetone, cooling the mixture with water, dropwise so that the pH is between 9.5 and 9.8. Additionally, 35 ml 3N is required. NaOH.
    Editor M.Nedoluzhenko
    Order 8548/61 Circulation 379 Subscription
    VNIIPI USSR State Committee
    for inventions and discoveries 113035, Moscow, Zh-35, Raushsk nab., 4/5
    Branch PPP Patent, Uzhgorod, st. Project, 4
    0
    five
    five
    0
    five
    0
    five
    After stirring for 2 hours at room temperature, the final pH is 9.5. The acetone is evaporated, the mixture is poured and the aqueous phase is acidified with hydrochloric acid (1: 1), then extracted with ethyl acetate. The mixture is evaporated and the residue is recrystallized from chloroform-hexane to obtain the pure compound, so pl. 134-137 s.
    c) D - (-) - M-isopropoxycarbonyl-phenylglycine.
    -
    113.1 g of D - (-) - phenylglycine are suspended in 1 l of water and the pH is adjusted to 10.2-10.4 with 50% NaOH, cooled (ice water) and the mixture is stirred. At the same time, 225 ml of isopropyl chloroformate and 50% sodium hydroxide are added so as to maintain the pH at the indicated level. Then the reaction mixture is alkalinized to pH 12-13 and the pH is stirred with this for 40 minutes. The practically clear solution is acidified with concentrated hydrochloric acid while cooling to the appearance of turbidity. The mixture was seeded to start crystallization and after 20 minutes the pH was further lowered to 2.0. After 30 minutes from the beginning of crystallization, the mixture is filtered, the residue is washed with 100 ml of water and dried in a vacuum cabinet over silica gel at a temperature of 50-60 ° C, then dried for another 16-17 hours at 60-70 ° C, . 116-120 s (of zn acetate).
    Compiled by I.Hropov
    Tehred T. Tulik Proofreader O. Lugov
    权利要求:
    Claims (2)
    [1]
    1. METHOD FOR PRODUCING Phenylglycine Derivatives of the General Formula
    ABOUT
    IN 2 -HC1 where R is a hydrogen atom or an oxy group, by the interaction of the corresponding phenylglycine derivative with an inorganic acid chloride in an inert organic solvent, followed by treatment of the intermediate with gaseous hydrogen chloride in an inert organic solvent, characterized in that, in order to simplify the process, as the phenylglycine derivative is a compound of the general formula -CH-COOH ^ R NH-C-0-Rj
    II about where R has the indicated meanings;
    R ( - lower alkyl or benzyl, as, inorganic acid chloride - thionyl chloride and the process is carried out in the presence of trichloroacetic or and-toluenesulfonic acid.
    [2]
    2. The method of pop. 1, characterized in that the processing of the intermediate product is carried out in an environment of dioxane, toluene or mixtures thereof.
    Priority by recognition to ”a m: 04.25.79 when R is a hydrogen atom; 09/04/79 when R is an oxy group.
    >
    eleven
    类似技术:
    公开号 | 公开日 | 专利标题
    RU2066324C1|1996-09-10|Crystalline azithromycin dehydrate, and process for preparation thereof
    SU1405705A3|1988-06-23|Method of producing 7-chloro-dioxylinecomycine in the form of its hydrochloride
    SU1205760A3|1986-01-15|Method of producing derivatives of phenylglycine
    SU651704A3|1979-03-05|Method of obtaining derivatives of dibenzocycloheptene, racemate or optically active salts thereof
    SU613725A3|1978-06-30|Method of obtaining 3-iminomethylrifamycin derivatives
    SU719499A3|1980-02-29|Method of preparing 1,2,3,4,6,7-hexahydro-11 b alpha-h-benzo|-quinolysin derivatives or their salts
    US4115648A|1978-09-19|2,5-Dihydroxy benzene sulfonic acid mono esters
    SU542474A3|1977-01-05|The method of obtaining derivatives of 7-amino-3-cephem-3 -4-carboxylic acid or their salts
    US4865765A|1989-09-12|Ursodeoxycholic acid derivatives and their inorganic and organic salts having therapeutic activity, and process for preparing the same
    SU1272988A3|1986-11-23|Method of producing ergolines or physiologically acceptable salts thereof
    US2772280A|1956-11-27|Synthesis of 4-amino-3-isoxazolidone and its derivatives
    SU703024A3|1979-12-05|Method of preparing dimeric 1-formylindole dihydroindole or its salts
    EA008883B1|2007-08-31|A process for the preparation of chirally pure n-|-d-phenylalanine and crystalline modifications thereof
    US2650232A|1953-08-25|2-methyl-3-amino-4,5-di-hydroxymethylpyridine and its salts and the preparation thereof
    US3299095A|1967-01-17|1-benzyl tetramic acid derivatives
    SU543355A3|1977-01-15|The method of obtaining derivatives of glucose
    US2740781A|1956-04-03|3, 26-dihydroxy-16, 22-imino-5-cholestenes, 3, 26-dihydroxy-16, 22-imino-5, 16, 20|-cholestatrienes and derivatives thereof
    US4346045A|1982-08-24|Process for resolving DL-S-benzoyl-β-mercaptoisobutyric acid, and products obtained
    SU502607A3|1976-02-05|The method of obtaining lactams
    US4272454A|1981-06-09|Process for the chlorination of α-aminoacids
    KR920004137B1|1992-05-25|Process for preparing imidazole derivatives
    SU1268580A1|1986-11-07|Method of producing derivatives of 1-hydroxy-2-oxo-1,2-dihydropyrazine
    SU470957A3|1975-05-15|The method of obtaining 4-aminopyrrolin-3-one-2 derivatives or their salts
    RU1772103C|1992-10-30|Method of 2-aminobenzonitrile synthesis
    US3870708A|1975-03-11|Amine derivatives of penicillins and the method of their production
    同族专利:
    公开号 | 公开日
    EP0018546A2|1980-11-12|
    ES497800A0|1982-05-01|
    NO801171L|1980-10-27|
    PL223724A1|1981-02-13|
    CS214660B2|1982-05-28|
    FI801325A|1980-10-26|
    US4708825A|1987-11-24|
    YU41508B|1987-08-31|
    IL59902A|1983-11-30|
    PH22327A|1988-07-29|
    YU113580A|1983-06-30|
    EP0018546B1|1983-09-28|
    AU5772880A|1980-10-30|
    PL129239B1|1984-04-30|
    FI73968B|1987-08-31|
    DE3065012D1|1983-11-03|
    ES490858A0|1981-07-16|
    ES8204410A1|1982-05-01|
    DD151446A5|1981-10-21|
    IE800822L|1980-10-25|
    NO148920B|1983-10-03|
    EP0052094A1|1982-05-19|
    CA1148535A|1983-06-21|
    IL59902D0|1980-06-30|
    NZ193510A|1983-02-15|
    IE50176B1|1986-03-05|
    AU541678B2|1985-01-17|
    PT71129A|1980-05-01|
    EP0018546A3|1980-12-10|
    ES8106126A1|1981-07-16|
    FI73968C|1987-12-10|
    NO148920C|1984-01-11|
    MA18815A1|1980-12-31|
    AR228135A1|1983-01-31|
    DK174580A|1980-10-26|
    EP0084611A1|1983-08-03|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE500436C|1928-02-11|1930-06-20|I G Farbenindustrie Akt Ges|Process for the preparation of amino acid chlorides|
    US2516145A|1947-10-07|1950-07-25|Du Pont|Synthesis of n-carboanhydrides of alpha-amino acids|
    KR780000197B1|1972-12-26|1978-05-26|Bristol Myers Co|Method for preparing antibacterial agent|
    JPS5069039A|1973-10-23|1975-06-09|
    US3970651A|1974-01-07|1976-07-20|Bristol-Myers Company|Crystalline cephalosporin derivative|
    US3925418A|1974-06-19|1975-12-09|Bristol Myers Co|Hemisolvate of D--2-glycyl chloride hydrochloride and process|
    FI773020A|1977-10-12|1979-04-13|Fermion Oy|FOERFARANDE FOER FRAMSTAELLNING AV D-2- GLYCINCHLORIDE-HYDROCHLORIDE-DIOXANHEMISOLVAT|FR2493837B1|1980-11-13|1984-04-13|Sanofi Sa|
    FR2500827B1|1981-03-02|1984-01-06|Sanofi Sa|
    JPH0333149B2|1985-08-27|1991-05-16|Kanegafuchi Chemical Ind|
    DE3628795A1|1986-08-25|1988-03-03|Hoechst Ag|NEW THYRONE DERIVATIVES|
    IT1282955B1|1996-05-03|1998-04-02|Abres Associated Biotechnology|PROCESS FOR THE PREPARATION OF UREIDIC DERIVATIVES AND SUMMARY INTERMEDIATES|
    EP1678186A4|2003-10-30|2007-04-25|Cj Corp|Processes for the preparation of cephem derivatives|
    DE60325866D1|2003-11-28|2009-03-05|Xenocs S A|Method for producing an impression die and impression die|
    CN101613300A|2008-06-25|2009-12-30|河南新天地药业有限公司|Left-handed D-pHPG acyl chloride hydrochloride crude product synthetic technology|
    CN101613293A|2008-06-25|2009-12-30|河南新天地药业有限公司|Left-handed D-pHPG acyl chloride hydrochloride technique for purifying crude|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    AT308979A|ATA308979A|1979-04-25|1979-04-25|METHOD FOR PRODUCING-PHENYLGLYCYLCHLORIDE HYDROCHLORYD DERIVATIVES|
    AT585179A|AT372939B|1979-09-04|1979-09-04|METHOD FOR PRODUCING-- PHYDROXYPHENYLGLYCYL CHLORIDE HYDROCHLORIDE|
    AT585279A|AT372940B|1979-09-04|1979-09-04|METHOD FOR PRODUCING-- PHYDROXYPHENYLGLYCYL CHLORIDE HYDROCHLORIDE|
    [返回顶部]