• 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 present invention relates to methods for the preparation of anilinofumarate, a useful intermediate in the preparation of quinoline-2,3-dicarboxylic acid and in the preparation of 2-(2-imidazolin-z-yl) quinoline-3-carboxylic acid herbicidal agents.
    公开号:SU1736334A3
    申请号:SU4203226
    申请日:1987-08-28
    公开日:1992-05-23
    发明作者:Рой Молдинг Дональд
    申请人:Американ Цианамид Компани (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to an improved method for producing alkyl-aniline fumarates, compounds used as intermediates for the synthesis of quinoline-2,3-dicarboxylic acids, precursors of pyridine- and quinoline-imidazoline germicidal substances.
    A known method for producing alkyl-anilnum fumarates by reacting aniline with ketoesters and dialkylamino-dicarbokshgatami. Such as, for example, diethyloxalacetate and diethyl ether aceylenedicarboxylic acid. However, their availability is limited.
    The purpose of the invention is to simplify the process.
    This goal is achieved by using more available dichlorosuccinate and aniline reagents to form the anilinofumarate.
    The method of obtaining alkylamino fumarate by the formula
    CHCQOR 4ffl-C-CQQR
    ()
    one
    oo
    05
    with so
    J

    s
    where R is C —C-alkyl,
    carried out using an aliphatic dicarboxylic acid ester and aniline in an inert organic solvent at boiling, and dichlorosuccinate of the general formula
    C1-GH-GOOR HOOK-COOR
    18
    where R is C C -alkyl, which is reacted with a threefold molar excess of amine of the general formula
    R, R2NH, No.
    where RJ and R2 are hydrogen or C -C-al-and-kil, provided that only one of R, j and R2 is hydrogen, or R | and R "taken together
    five
    20
    Examples 2-4. Ethyl diethyl ether floor and 3-diethylamino succinic acid diethyl ester
    Cl-fH-GOiCiHj + (CtH CCH-OODNd / D
    HC-SOD + (Tt-C
    Shn-s-SOGS
    Liethylamine (2.41 g, 0, is added dropwise to the solution of tartaric acid diethyl ester (2.59 g, 0 15 ml of toluene).
    After cooling the reaction temperature at room temperature, water and water (15 ml) are separated and the mixture is evaporated under pressure to obtain 2.07 g of diethyl ether diethyl acid and indicated in chloramine ester
    with the nitrogen atom to which they are bonded, form five or six "" bj X liS l f ".L in VXJ 4-Ј GUL E WJOOJDIU
    the membered ring containing 25 is heated at 80-85 ° C for 8 hours; no more than two heteroatoms are consumed,
    for 8 hours at boiling point and the resulting mixture of alkylamino maleate or alkylamino fumarate of the general formula
    JJH-COOR.
    RiRtu-c-cooR
    and chloraminosuccinate of the general formula
    Cl-Ctt-COOR
    U & U-CH-COOR
    subjected to interaction with a molar equivalent of aniline in an inert organic solvent containing an organic acid, at 80-85 ° C for 4 hours.
    Example 1. Preparation of dichlorosuccinate.
    H-CDQfyHs ethanol H-iboCzHs catalyst
     a-CR-CQOCiHs
    ci-k-eoociHs
    Chlorine gas is bubbled into a solution of diethyl maleate in ethylene dichloride containing ethanol (0.1-mo

    to

    five
    20

    personal equivalent). After the mixture was stirred at room temperature for 8 hours, it was flushed with nitrogen gas for 5 minutes, the solvent was removed under reduced pressure, to obtain dichlorosuccinate in 94% yield.
    Examples 2-4. Preparation of diethylamino maleic acid diethyl ether and 2-chloro-3-diethylamino-succinic acid diethyl ester
    Cl-fH-GOiCiHj + (CtH5) iNH CCH-OODNd / D
    HC-SOD + (Tt-ChCOiCtfs
    shn-s-sOGSy (sd-so & ts
    n Liethylamine (2.41 g, 0.033 mol) is added dropwise to a stirred solution of diethyl dichloric tartaric acid (2.59 g, 0.01 mol) in 15 ml of toluene. The resulting mixture
    and then boiling under reflux for 3 hours. After cooling the reaction mixture to room temperature, it is washed with water (15 ml), the toluene layer is separated and evaporated under reduced pressure to give 2.07 g (85%) of diethylamino maleino diethyl ether mixture - howl acid and title succinic ester of succinic acid
    35 with a ratio of maleate and succinate equal to 7.51.
    Using the above procedure and replacing the corresponding amine with diethylamine, the products listed in the table are obtained.
    “ЬЈ чГ X liS Л f“ .L at VXJ Ь4- ЬГЪЛ Э WJOOJDIU
    25 heated at 80-85 ° C 8 h 30
    Fumarate example
    5. Getting aniline
    no-seven
    ShgNv-SogS
    &
    ns-sogs5
    (C H-C-COiCiHs
    SPLA
    GzH5OzCCH
    Aniline (0.93 g, 0.01 mol) is added to a solution of acetic acid (3.0 g, 0.05 mol) in 20 ml of toluene and a mixture of diethylamino maleic acid diethyl ether and 2-chloro-3-diethylaminate diethyl ether. acid. The resulting solution is heated at 80-85 ° C for 4 hours. After cooling the reaction mixture to room temperature, it is washed with water (10 ml) and then with an aqueous solution of hydrogen chloride (12% by weight, 2 ml).
    According to the analysis of the obtained toluene solution by gas-liquid chromatography and isolation of the product, it was found that the total yield over all stages, starting with diethyl metalate, is 69%.
    Example 6. Preparation of diethyl oxalacetate and subsequent preparation of diethylaniline fumarate.
    17 airshad
    (Shk-s-hell,
    n-moSa (sha-with-with
    Hifl-coififls
    o i-coi№
    adgot
    H-iUo & V
    aniline
    Toluene solution — 15 ml of a mixture of diethylamine diethylamino maleic acid and diethyl ether 2-chloro-3-diethylamino-succinic acid (2.43 g, 0.01 mol) is stirred with water (5.0 g) containing 2.15 g (0.015 mol) of concentrated hydrochloric acid, for 2 h 30 min. . The toluene layer containing diethyloxalacetate is separated and aniline (0.93 g, 0.01 mol) is added. The resulting solution is stirred at room temperature for 30 minutes and then heated to reflux for 1 hour and 30 minutes, and the water formed is collected in a Dean and Stark trap. Analysis of the cooled toluene solution by gas-liquid chromatography showed that the yield of diethylaniline fumarate is 55%.


    36334
    ten
    15
    20
    25
    thirty
    35
    40
    Example 7. Obtaining quinoline-2,3-dicarboxylic acid.
    Vilsmaier reagent is prepared by adding 4.61 g (0.03 mol) GOSP phosphorus oxychloride dropwise to a solution of 2.19 g (0.03 mol) of dimethylformamide in 12 ml of toluene, maintaining the temperature at 20-30 ° C. These two layers are stirred at 20-30 ° C for 60 minutes and then treated, dropwise, with a solution of 5.26 g (0.02 mol) of anilino fumaric acid diethyl ester in 40 ml of toluene, maintaining the temperature at 20-30 ° C . The solution, which is formed by heating, is refluxed for 2 hours, cooled until the condensate has stopped, and poured into 60 ml of water. The dark, syrupy material that settles is dissolved, with stirring, for 30 minutes at room temperature. Analysis of the toluene solution by gas-liquid chromatography showed that the yield is 72%. Upon evaporation of the diester solution, an oily low melting solid is formed, which, upon recrystallization from isopropyl alcohol, gives 4.05 g of a brown solid. M.p. 53-56 ° C.
    The two phases, which formed from 4.1 g (0.015 mol) of the diester in 25 ml of toluene and 16 ml of a 15% sodium hydroxide solution, are heated to reflux with good stirring for 8 hours. The two phases are cooled to 50%. 55 ° C and diluted with water (20 ml). The aqueous phase is separated and added dropwise to 11 ml of 35% sulfuric acid, keeping the temperature lower than 40 ° C, and the resulting thick mixture is filtered, the solid is collected and dried overnight at 45–60 ° C and a pressure of 30 -50 mmHg to obtain quinoline-2,3-dicarboxylic acid with a yield of 3.19 g.
    权利要求:
    Claims (1)
    [1]
    The implementation of the proposed method makes it possible to obtain alkylaniline fumarate from the available products, with a good yield, and thus simplifies the process of obtaining valuable pyridine- and quinoline imidazoline herbicidal substances. Invention Formula
    The method of obtaining alkylaminomers General formula
    (MOOR fVffl-C-GOOR
    where R is C -C-alkyl, using an aliphatic dicarboxylic acid ester and aniline in an inert organic solvent at boiling, characterized in that, to simplify the process, dichloro succinate of the general formula is used as an ester
    CI-CH-CQOR
    ci-k-eooR
    where R is C C -alkyl, which is reacted with a threefold molar excess of amine of the general formula
    R, R2NH,
    where X and R2 are hydrogen or alkyl, provided that
    is hydrogen, or R, (and R2, taken together with the nitrogen atom to which they are bound, form a five- or six-membered ring containing not more than two heteroatoms,
    for 8 hours at boiling point and the resulting mixture of alkylamino malate or alkylamino fumarate of the general formula
    15
    CH-COOR RtRjK-C-COOR
    and chloraminosuccinate of the general formula
    2
    CI-CH-CQQR RWHH-COOR
    subjected to interaction with a molar equivalent of aniline in an inert organic solvent containing an organic acid, at 80-85 ° C in those
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US3929432A|1970-05-29|1975-12-30|De Beers Ind Diamond|Diamond particle having a composite coating of titanium and a metal layer|
    DE3276432D1|1981-03-24|1987-07-02|Ciba Geigy Ag|Acyl quinolinone derivatives, processes for their preparation, pharmaceutical compositions containing them and their use|
    US4459409A|1982-05-25|1984-07-10|American Cyanamid Company|Process for the preparation of 2,3-quinolinedicarboxylic acids|
    US4518780A|1982-05-25|1985-05-21|American Cyanamid Company|Process for the preparation of 2-nicotinic acids and quinoline-3-carboxylic acids|US4843162A|1982-05-25|1989-06-27|American Cyanamid Company|Alkyl esters of substituted 2-methyl-3-quinolinecarboxylic acid and quinoline-2,3-dicarboxylic acid|
    US4910327A|1982-05-25|1990-03-20|American Cyanamid Company|Alkyl esters of substituted 2-methyl-3-quinolinecarboxylic acid and quinoline-2,3-dicarboxylic acid: dialkyl 3-phenylaminobut-2-ene-dioates and methods for the preparation thereof|
    US5001254A|1986-08-29|1991-03-19|American Cyanamid Co|Novel method for the preparation of quinoline-2,3-dicarboxylic|
    US4847405A|1987-03-19|1989-07-11|American Cyanamid Company|Method for the preparation of anilinofumarate [quinoline-2,3- dicarboxylic]|
    US4814486A|1987-10-01|1989-03-21|American Cyanamid Company|Method for the preparation of anilinofumarate|
    DE3872136T2|1987-10-01|1992-12-03|American Cyanamid Co|METHOD FOR PRODUCING DICHLORBERSTEINSAUREDIALKYLESTER.|
    US4904816A|1989-06-15|1990-02-27|American Cyanamid Company|Process for the manufacture of anilinofumarate via chloromaleate or chlorofumarate or mixtures thereof|
    US5322948A|1989-08-31|1994-06-21|Hoechst Celanese Corporation|Process for preparing pyridinecarboxylic acid derivatives|
    US5405987A|1989-08-31|1995-04-11|Hoechst Celanese Corporation|Process for preparing pyridine and quinoline derivatives|
    法律状态:
    2006-12-27| REG| Reference to a code of a succession state|Ref country code: RU Ref legal event code: MM4A Effective date: 20050829 |
    优先权:
    申请号 | 申请日 | 专利标题
    US06/902,274|US4675432A|1986-08-29|1986-08-29|Method for the preparation of anilinofumarate|LTRP984A| LT2505B|1986-08-29|1993-09-16|THE BACKGROUND OF ALKILANILINOFUMARATE RECEPTION|
    LV931142A| LV5699A3|1986-08-29|1993-10-08|Attenuation for obtaining aniline esters of aniline fumaric acid|
    MD94-0094A| MD116C2|1986-08-29|1994-04-27|Method of obtaining of alkylanikine fumarate|
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