• 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 relates to heterocyclic compounds, in particular to the preparation of 1-C3-mercapto- (25) -methyl-propionyl-pyrrolidine- (2S) -carboxylic acid, which has a blood pressure reducing effect. The goal is to increase the yield and purity of the target product. The preparation is carried out by the reaction of omega-halogen-acylproline with thiourea and subsequent hydrolysis of the isothiuro1-nium compound thus obtained. The process is carried out in an organic dipolar alroton solvent, such as N, N (-dimethylformamide, M, m -dimethylacetamide or dimethylsulfoxide.
    公开号:SU1650007A3
    申请号:SU874202836
    申请日:1987-06-26
    公开日:1991-05-15
    发明作者:Фишер Янош；Фодор Тамаш；Добаи Ласло；Штефко Бела
    申请人:Эгиш Дьедьсердьяр (Инопредприятие)；
    IPC主号:
    专利说明:

    This invention relates to an improved process for the preparation of 1-Gz-mercapto- (2S) -methylpropionyl-pyrrolidine- (23) -carboxylic acid (captopril), which has a blood pressure reducing effect.
    The purpose of the invention is to increase the yield and purity of the target product by carrying out the process in an organic dipolar aprotic solvent, such as M, K-dimethylformamide, NjN-dimethylacetamide, or methyl sulfoxide G
    The invention is illustrated by the following examples.
    Example 1. 1- 3-mercapto- (28) -methyl-propionyl-pyrrolidine- (2S) -carboxylic acid.
    10.56 g (0.0374 mol) of 1-3-bromo- (2) -methylpropionyl-pyrrolidine- (2S) carboxylic acid and 3.04 g (0.0040 mol) of thiourea are dissolved in 30 ml of M, N- dimethylacetamide in a nitrogen atmosphere, the reaction mixture is stirred at 60 ° C in a nitrogen atmosphere for 15-20 hours. The solvent is evaporated under reduced pressure and the residue is dissolved in 50 ml of distilled water. While cooling with ice water and under nitrogen atmosphere, 6.00 g (0.12 mol) of hydrazine hydrate is added to the resulting solution, the reaction mixture is stirred for 30 minutes while cooling with ice-water, and the next 30 minutes at room temperature. To the reaction mixture are added 100 ml of a 5% aqueous solution of sulfuric acid, the white precipitate is filtered off, washed with water and then with dichloromethane. The filtrate is extracted four times05
    SP
     s
    Dissolve the dichloromethane portions in SO2 ml9 (the combined organic solutions are washed twice with water in 20 ml portions and the organic phase is extracted twice with 15 ml dichloromethane. The organic phases are combined, dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. 7.54 g (99% of theory) of the oil remains, from which 25 ml of trichloroethylene is recrystallized.
    So, get 6.10 g of the target product.
    ten
    The precipitated precipitate is filtered with water and then dichlorum 10 g of chlorate sodium is added to the aqueous phase and the mixture is diluted four times with dichloromethane in portions of 30 ml. The combined organics are dried over anhydrous magnesium sulfate, filtered, and evaporated under reduced pressure. The remainder is recrystallized from 20 ml of chloroethylene.
    This gives 3.33 g of the target tar which melts at 106
    a product that melts at 104-106 C-j. The yield is 82% of theory.
    20
    2S
    thirty
    The yield is 80% of theory. BO -129.5 ° (, ethanol). EXAMPLE 2. 1-Gz-Mercapto- {23) - methylpropionyl-3-pyrrolidine- (28) -carboxylic acid.
    2.64 g (0.01 mol-3-bromo (28) -methylpropionic) -pyrrolidine- (2S) -carboxylic acid and 0576 g (0.01 mol) of thiourea are dissolved in K) ml of dimethyl sulfoxide and the resulting solution; stirred at 60-70 ° C for 24 hours, then treated with 30 ml of 10% sodium hydroxide solution and stirred for an hour. The pH is adjusted with a 20% hydrochloric acid solution under ice-cooling, and the solution is extracted four times with dichloromethane in 20 ml portions, dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure. The residual oil is recrystallized from trichlorethylene.
    Thus, 1.64 g of the title compound is obtained, which melts at 104-106 ° C. The yield is 81% of theory. S Ј -129.5 ° (, ethanol).
    Example 1- 3-Mercapto- (28) -methylpropionide -pyrrolidine- (28) -carboxylic acid.
    5.28 g (0.02 mol) 1- | 3-bromo- (2S) -methylpropionyl-nrrolidine (2S) -carboxylic acid and 1E67 g (0.022 mol) of thiourea are dissolved in 15 ml of N, N-dimethylformamite, the resulting solution is stirred at 60 ° C for 24 hours. Solvent evaporation under reduced pressure, the residue is dissolved in 30 ml of distilled water, the resulting solution is treated with 6.00 g of a 60% hydrazine solution while being cooled with ice water and slowly stirred during the next hour while cooling. 60 ml of a 5% sulfuric acid solution are added to the reaction mixture.
    45
    55
    SF 129.5e (, ethanol)
    Example 4. A. 1- (28) -Me isothiouranium propenyl-pyrrole or carboxylate
    5.64 g of CO, 02 mol of 1-Ј3-bromo- (28) -methylpropionyl | lidine (25) carboxylic acid monohydra is p-rted in 50 ml of dchloromethane, the semi-solution is mixed with 5 g of aqueous magnesium sulfate for over. The drying agent is filtered off with 10 ml of dichloromethane, the combined solutions are combined and the mixture is reduced under reduced pressure. The solution was dissolved in 15 ml of anhydrous M methylformamide, treated with 1, (0.02 mol) anhydrous thiouma and stirred for 24 hours in a 2% nitrogen stream. During the reaction, the temperature in the flask with the reaction mixture is maintained at an oil level of not 70 ° C. The mixture is then cooled with ice and diluted with 2.8 ml (0.02 mol) of triethipamine in 20 ml of tonitrile with stirring in those 30-40 minutes. The reaction mixture was perched for the next 2 hours, the filter cake was suspended in 2 acetonitrile5, filtered, again washed with 20 ml of acetonitrile, filmed and dried. Thus, 4 target compounds are obtained, which are at 187-189 ° C. The yield is from theory.
    MPE 1 ° (, acetic acid4. Thin layer chromatography of a mixture of pyridine, water and glacial hydrochloric acid in the ratio of 20: 11-6 ethyl acetate -, M; mixture of bottles
    glacial acetic acid and in
    la
    in the ratio 7: 1: 43, 2.
    you, the precipitated precipitate is filtered off, washed with water and then with dichloromethane. 10 g of sodium chloride are added to the aqueous phase and the mixture is extracted four times with 30 ml of dichloromethane. The combined organic phases are dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure. The residual oil is recrystallized from 20 ml of trichloroethylene.
    Thus, 3.33 g of the title compound is obtained, which melts at 106 ° C.
    The yield is 82% of theory.
    SF 129.5e (, ethanol)
    Example 4. A. 1- (28) -Methyl-3-isothiouronium propenyl-pyrrolyl- (2S) -carboxylate
    0
    S
    0
    40
    45
    5.64 g of CO, 02 mol of 1-Ј3-bromo- (28) -methylpropionyl | pyrrolidine (25) carboxylic acid monohydrate is dissolved in 50 ml of dchloromethane, the resulting solution is mixed with 5 g of magnesium sulfate base for hours The drying medium is filtered, washed with 10 ml of dichloromethane, the organic solutions are combined and evaporated under reduced pressure. The residue is dissolved in 15 ml of anhydrous M, i-dimethylformamide, treated with 1.52 g (0.02 mol) of anhydrous thioumara and stirred for 24 hours in an atmosphere of nitrogen. During the reaction, the temperature in the flask with the reaction mixture was maintained at an oil bath of 70 ° C. The mixture is then cooled with ice water and diluted with 2.8 ml (0.02 mol) of triethipamine in 20 ml of acetonitrile with stirring for 30-40 minutes. The reaction mixture is stirred for the next 2 h, the filter cake is filtered off, suspended in 20 ml of acetonitrile, filtered, again suspended in 20 ml of acetonitrile, filtered and dried. Thus, 4.2 g of the title compound are obtained, which melt at 187-189 ° C. The yield is 81% of theory.
    Mse 1 ° (, acetic acid4. Thin-layer chromatography; 6 h of a mixture of pyridine, water and glacial acetic acid in the ratio of 20: 11-6.4 h, ethyl acetate -, M; mixture of butanoled acetic acid and water
    la
    in the ratio 7: 1: 43, 2.
    . 1-Ј3-Metzuto- (25) -methylpropiopyrrole- (23) -carboxylic acid.
    2 ml (0.02 mol) of 50% hydrazine are added in a droplet to a stirred and cooled with ice water solution of 2959 g (0.01 mol) of 1- (2S) -methyl-3-isothiuronium propiokyl} -pyrrolidine - (23) -carboxylate in 25 ml of water in the atmosphere of Achota. The reaction mixture is stirred for another 30 minutes while cooling, then the cooling bath is removed and the mixture is stirred
    extracted with 20 ml vop.y. The organic phase is dried over anhydrous magnesium sulphate and evaporated. 6.40 g (95% of theory) of 1-Hz-bromo-2-methylpropionyl-pyrrolidine- (2) -carboxylic acid benzyl ester are obtained in the form of a pale yellow oil.
    Thin layer chromatography: silica gel, 3 parts of benzene, T. of the following acetic acid: 44 and 0.48, the ratio of diastereoisomers is 1: 1.
    The resulting oil is dissolved in 60 ml of ethyl acetate and to solution to
    30 min. The reaction mixture is cooled again. 0.6 g of 10% palladium is added to the mixture and the mixture is treated to 10 ° C and treated with a mixture of saturated coal 8 as a catalyst and 2 ml of concentrated hydrochloric acid. The suspension is hydrogenated at
    lots and 2 ml of water and stirred for 30 minutes. After adding 6-10 g of sodium chloride, the product is extracted three times with dichloromethane in 20 ml portions. The organic solutions are combined, washed with 15 ml of water and the aqueous phase is extracted with 5 ml of dichloromethane. The organic phases are combined, dried over anhydrous magnesium sulphate, filtered and evaporated under reduced pressure. (2.03 g of an oily residue is recrystallized from 10 ml of trichlorethylene. The crystals are washed with n-hexane and dried.
    Thus, 1.62 g of the title compound is obtained, which melts at 103 - 104 ° C. The yield is 80% of theory.
    "
    (XJs -129-130 ° (, ethanol). Preparation of the starting compound: 1-GZ-bromine monohydrate of (23) -methyl-pro-pyOH-β-pyrrschidine- (23) -carboxylic acid.
     3.34 (0.02 mol) of 3-bromo-2-methyl-propionic acid and 4.60 g (0.02 mol) of (H) -roline benzyl ester hydrochloride are dissolved in 50 ml of anhydrous d-sul-methane and to obtain the mu solution, add a mixture of 1.9 g of triethyla a and 5 ml of anhydrous dichloromethane and then 3.92 g of (0.01 / 9 mol) dissolved in doshormetane (20 ml) of N-di-cyclohexyl-carbodiimide at 0 ° C with stirring and cooling. The reaction mixture was stirred for another 2 hours at 0 ° C and then for another 12 hours at room temperature. The reaction mixture is filtered and the filtrate is extracted with 20 ml of 9% hydrochloric acid solution, 20 ml of water, 5% sodium hydrogen carbonate solution, l immediately after
    komkatnoy temperature and at atmospheric pressure. When the starting compound is no longer detectable by thin layer chromatography, the catalyst is filtered off, washed with ethyl acetate, the organic solvent is evaporated and the residue is recrystallized from water. Thus, 2.00 g of the title compound is obtained, which melts at 69-72 C.
    The yield is 42.5% of theory. ry-jЈS -88.1 ° (, ethanol).
    thirty
    权利要求:
    Claims (1)
    [1]
    Invention Formula
    The method of obtaining 1- 3-mercapto- (2S) -methylpropionic {-pyrrolidine, - (2S) - carboxylic acid of formula
    9nz
    (S) HS-CH2-CH-CO-N-S
    soon
    cs)
    U
    the interaction of omega-halogen-acyl-proline formula
    CH-,
    1 JK1
     Hotl-CHj-CH-CO-N-UNV (S, O
    with t urea and subsequent hydrolysis of the isothiourium compound thus obtained with the formula
    ,with
    sn,
    2 / C-S-CH9-CH-CO-N-fCOOH 55 HN (S) O
    characterized in that, in order to increase the yield and purity of the target product, the process is carried out in
    716500078
    organic dipolar aprotein tilformamide, M.L.-dimethylacetamide
    a solvent such as N.N-dime or dimethyl sulfoxide.
    类似技术:
    公开号 | 公开日 | 专利标题
    PL101471B1|1978-12-30|METHOD OF MAKING PYROLIDINE DERIVATIVES
    CH624932A5|1981-08-31|
    US4297282A|1981-10-27|Resolution of mercaptopropionic acids
    JP2691442B2|1997-12-17|Novel proline derivative
    SU719499A3|1980-02-29|Method of preparing 1,2,3,4,6,7-hexahydro-11 b alpha-h-benzo|-quinolysin derivatives or their salts
    SU1650007A3|1991-05-15|Method of producing 1-[3-mercapto-|-methylpropionil]-pyrrolidin-| carbonic acid
    SU1360583A3|1987-12-15|Method of producing pyrrolidinone derivatives
    EP0154490B1|1988-08-10|Process for the preparation of pyrrolidone derivatives
    US5110936A|1992-05-05|Process for the preparation of 3-|-l-thiazolidine-4-carboxylic acid derivatives
    SU888819A3|1981-12-07|Method of preparing derivatives of 5|-acylated benzimidazolcarboxylic-2 acids or their salts
    US4614806A|1986-09-30|Process for the asymmetric synthesis of chiral indoline-2-carboxylic acids
    Yamada et al.1978|Preparation of d-p-Hydroxyphenylglycine: Optical Resolution of dl-p-Hydroxyphenylglycine by Preferential Crystallization Procedure
    US5585500A|1996-12-17|Method of producing optically active pyrrolidines with high enantiomeric purity
    KR20000062263A|2000-10-25|Method of preparation of physostigmine carbamate derivatives from eseroline ethers
    US4456611A|1984-06-26|Derivatives of 2-[3-|2-amino propionyloxy] acetic acid, and seritoning increasing use thereof
    SU843738A3|1981-06-30|Method of preparing derivatives of aminopyrrole or its salts
    US4139700A|1979-02-13|Process for the preparation of bicyclothiadiazinones
    KR19980702282A|1998-07-15|Process for the preparation of indolin compounds and intermediates for their preparation
    KR100399854B1|2003-12-18|An Arthropodicidal Oxadiazine Intermediate
    US5202443A|1993-04-13|Process for preparing 1-|-3-mercapto-methyl-1-oxopropyl)-l-proline
    JPH069553A|1994-01-18|Preparation of 1-|- pyrrolidine-2s-carboxylic acid
    US3870708A|1975-03-11|Amine derivatives of penicillins and the method of their production
    US4727183A|1988-02-23|Process for the asymmetric synthesis of chiral α-hydroxy-2-nitrobenzenepropanoic acid
    SK13592001A3|2002-11-06|Synthesis of 3-amino-3-aryl propanoates
    SU351369A1|METHOD OF OBTAINING ALKALOIDS
    同族专利:
    公开号 | 公开日
    CS276394B6|1992-05-13|
    NO168941B|1992-01-13|
    ATA91186A|1992-01-15|
    FI872859A|1987-12-28|
    IT8721085D0|1987-06-26|
    CH673279A5|1990-02-28|
    JPS6327475A|1988-02-05|
    IT1206792B|1989-05-03|
    NO872690L|1987-12-28|
    PL266478A1|1988-06-09|
    FI872859A0|1987-06-26|
    AT395012B|1992-08-25|
    DE3721430A1|1988-01-28|
    FI87770C|1993-02-25|
    GR871012B|1987-11-02|
    YU46319B|1993-05-28|
    HUT44490A|1988-03-28|
    ES2004451A6|1989-01-01|
    DK329787D0|1987-06-26|
    CN87104388A|1988-03-02|
    AT387381B|1989-01-10|
    DK329787A|1987-12-28|
    KR880000392A|1988-03-25|
    DD263757A5|1989-01-11|
    SE462751B|1990-08-27|
    AR243159A1|1993-07-30|
    SE8702654D0|1987-06-26|
    NO872690D0|1987-06-26|
    FI87770B|1992-11-13|
    PT85190A|1987-07-01|
    KR900007217B1|1990-10-05|
    CS479487A3|1992-01-15|
    PT85190B|1990-03-30|
    SE8702654L|1987-12-28|
    ATA162087A|1988-06-15|
    PL153449B1|1991-04-30|
    YU118187A|1988-04-30|
    HU196959B|1989-02-28|
    NO168941C|1992-04-29|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE4123172A1|1990-09-21|1992-04-02|Egyt Gyogyszervegyeszeti Gyar|METHOD FOR PRODUCING 1----PROPIONYL) -PYRROLIDINE--CARBONIC ACID|AU509899B2|1976-02-13|1980-05-29|E.R. Squibb & Sons, Inc.|Proline derivatives and related compounds|
    IL58849A|1978-12-11|1983-03-31|Merck & Co Inc|Carboxyalkyl dipeptides and derivatives thereof,their preparation and pharmaceutical compositions containing them|
    GB2065643B|1979-12-13|1983-08-24|Kanegafuchi Chemical Ind|Optically active n-mercaptoalkanoylamino acids|
    IE54551B1|1982-01-22|1989-11-22|Ici Plc|Amide derivatives|
    KR860001391B1|1984-07-23|1986-09-22|보령제약 주식회사|Process for the preparation of pyrolidines|SE421551B|1980-03-26|1982-01-04|Sandvik Ab|DRILLING TOOL FOR ROTATION AND / OR DRILLING|
    JPH0149833B2|1985-11-21|1989-10-26|Kingu Purinteingu Kk|
    US6160008A|1996-09-26|2000-12-12|Meditor Pharmaceuticals Ltd.|Pharmaceutical compositions comprising S-alkylisothiouronium derivatives|
    CN103086939A|2011-10-28|2013-05-08|华中药业股份有限公司|Recrystallization method of 1-pyrrolidine-2-carboxylic acid|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    HU862689A|HU196959B|1986-06-27|1986-06-27|Process for producing merkapto-acyl-proline derivatives|
    [返回顶部]