• 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:
    Quinoxaline-1,4-derivatives are described having the general formula /I/ and biologically acceptable salts thereof, <IMAGE> wherein Q is hydrogen or methyl, R1 represents hydrogen, cyano, lower alkanoyl or nitro or halogen, R2 stands for cyano, lower alkanoyl, or a group of the general formula -COOR3, -CONR4R5 or -CO-NH-NR4R5, and R3 represents hydrogen or C1-18 alkyl, C6-12 aryl or C6-10 aryl-/C1-4 alkyl/ optionally substituted by halogen or hydroxy, whereby the aromatic ring of the said groups may optionally contain 1-3 identical or different substituents selected from lower alkyl or alkoxy, amino, nitro, halogen and/or hydroxy, R4 and R5 are various substituents, or R4 and R5 represent, together with the adjacent nitrogen atom, a 5 or 6 membered heterocyclic group optionally substituted by a further nitrogen or oxygen atom, with the proviso that if Q represents hydrogen and R2 stands for carboxy, R1 may denote only other than hydrogen. Processes for the preparation of the above compounds and fodder concentrates, fodder additives or fodders containing the said compounds are also described. The new compounds of the general formula /I/ possess weight-gain increasing and antibacterial effects and can be used to advantage in animal husbandry.
    公开号:SU1230468A3
    申请号:SU823472649
    申请日:1982-08-03
    公开日:1986-05-07
    发明作者:Бенко Пал；Божинг Даниель；Гундель Янош；Мадьяр Карой
    申请人:Эдьт Дьедьсерведьесети Дьяр (Инопредприятие)；
    IPC主号:
    专利说明:


    O4
    The invention relates to a method for producing new quinoxaline-1, 4-dioxide, which have properties that increase the weight of animals, and can be used in agriculture.
    The aim of the invention is a method for producing new quinoxa- lin-1,4-dioxide derivatives, possessing animal-weight-enhancing properties in a series of quinoxaline.
    Example 1. 15.85 g (0.12 mol of malonic acid monoethyl ester is mixed with 40 ml of pyridine. 19 g (0.1 mol of 2-formylchinoxalin-1,4-dioxide) are added with stirring and 0.86 g (0.8 0.01 mol) of piperidine. The reaction mixture is heated for 4 h, cooled and poured into ice-cold water. The precipitated product is filtered off, washed with water and acetone to give 19.5 g of ethyl ether, p- (2-, - quinoxaline-1, 4-dioxide) acrylic acid. Yield 75%, mp 190-191 ° C
    Example 2. A mixture of 13 g (0.05 mol) of ethyl ester of p- (2-α-quoxalinyl-1,4-dioxide) acrylic acid, 70 ml of methanol and 7 ml of 1N. an aqueous solution of sodium hydroxide. heated for half an hour at 50 ° C. The reaction mixture was cooled and the precipitated product was filtered off. 8.9 g of E- (2-quinoxalinyl-1,4-dioxide) acrylic acid methyl ester are obtained. Exit 73%, so pl. 207-208 S.
    Example 3. A mixture of 19 g (0.1 mol) of 2-formylquinoxalin-1,4-dioxide, 9.9 g (0.1 mol) of methyl ether-cyanoacetic acid, 160 ml of isopropanol and 3.5 ml of 10% aqueous The sodium hydroxide solution is heated at room temperature for 2 hours. The reaction mixture is cooled to 5 ° C and the precipitated product is filtered off. 22.1 g of ci-cyano-p -, (2-quinoxalinyl-1., 4-; dioxide) acrylic acid methyl ester are obtained. Output
    82%, Red crystals melt at 198-199 C.
    Example 4. The procedure of Example 3 is followed with the difference that 2-formylquinoxalin-1, 4-dioxide is introduced into
    interaction with cyanoenzoic acid ethyl ester. Ethyl ester of ci-cyano-p, - (2-quinox salinyl-1, 4-dioxid) acrylic acid is obtained with a yield of 85.5%, so pl. 160-161 ° C.
    Example 5. A mixture of 9.5 g (0.05 mol) of 2-formylquinoxalin-1,4-dioxide, 5.8 g (0.05 mol) of methyl acetoacetate, 120 ml of isopropanol and 2 ml of 10%
    The aqueous sodium hydroxide solution is stirred at room temperature for 2 hours. After cooling, the mixture is filtered. Obtain 10.8 g of methyl ester of os-acetyl-pr- (2-quinoxalinyl-1, 4-dioxide) acrylic 15, acids, Yield 75%, so pl. 159160 S. I
    Example 6. Follow the technique.
    of example 5 with the difference that instead of the methyl ester of acetoacetic acid used amide of cyanoacetic acid, A1CHID oi-cyano-3 - (2-quinoxaline-1,4-dioxide) acrylic acid
    get with the release of 75%, so pl. 212C
    . The results of the use of the proposed compounds are listed in the table.
    ; The table shows that five new
    compounds have an effective effect in terms of weight gain and p- (2-quinoxalinyl-1,4-dioxide) acrylic acid (s) of a similar structure does not increase the weight when it is added to
    stern.
    Example
    Test compounds
    p- (2-quinoxalinyl- -1,4-dioxide) ethyl ester of acrylic acid
    / 5 - (2-quinoxalinyl- -1, 4-dioxide) methyl ester of acrylic acid
    0 cyano- / 3- (2-quinoxalinyl-, 4-dioxide) methyl ester of acrylic acid
    oi-cyano-p- (2-quinoxinyl-1,4-dioxide) ethyl ester of acrylic acid
    j3 - (2-quinoxalinyl- -1,4-dioxide) acrylic acid 2,6-dimethyl-anilide
    Control (without active substance)
    Editor G. Volkova
    Compiled by T. Yakunin
    Tehred L. Serdgokova Corrector I. Erdeyi
    Order 2463/60 Circulation 379 Subscription
    VNIIPI USSR State Committee
    for inventions and discoveries 1П035, Moscow, Ж-35, Raushsk nab., 4/5
    Production and printing company, Uzhgorod, st. Project, 4

    Amount of feed giving 1 kg of Ari weight relative to the control group

    78.7 106.9 100.0 101, 0
    92.56 100.0
    权利要求:
    Claims (1)
    [1]
    METHOD FOR PRODUCING CHINOXALINE-1,4-DIOXIDE DERIVATIVES total / 81 sn = s h
    Where R, is hydrogen or a cyano group;
    R about is a group of the formula COOR ^, (in which RjC, -C ,, is alkyl, are distinguished by the fact that the compound of formula e
    reacted with a compound of the general formula
    R s —CH 2 —C0 — R 4 wherein R s is a carboxy group or a cyano group;
    R q is C, —Ci, alkoxy, in the presence of a base such as pyridine or an alkali metal hydroxide, in an organic solvent at a temperature from room temperature to 60 C.
    SU s, 1230468 A 3
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    同族专利:
    公开号 | 公开日
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    CA1184913A|1985-04-02|
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    DD159072A5|1983-02-16|
    US4409219A|1983-10-11|
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    AR231834A1|1985-03-29|
    IT1211050B|1989-09-29|
    GR75255B|1984-07-13|
    SE8103258L|1981-11-24|
    YU82383A|1983-12-31|
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    CH648025A5|1985-02-28|
    BR8103208A|1982-02-16|
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    GB2076401B|1984-05-31|
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    ES502909A0|1983-01-01|
    PL128382B1|1984-01-31|
    DK227281A|1981-11-24|
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    SU29924A1|1932-03-21|1933-04-30|М.Д. Жанков|Decorticator for stems of bast plants|
    US3371090A|1964-09-16|1968-02-27|Pfizer & Co C|Novel antibacterial agents|
    GB1308370A|1969-12-09|1973-02-21|Research Corp|1-hydroxy-3-oxo-benzimidazoles quinoxaline-di-n-oxides andbenzimidazole-mono-and di-n-oxides|
    US3493572A|1968-07-05|1970-02-03|Pfizer & Co C|Process for producing quinoxaline-di-n-oxides|
    US3926992A|1972-11-03|1975-12-16|Pfizer|Aldol products of 2-quinoxalinecarboxaldehy-1,4-dioxides|
    HU169299B|1974-11-21|1976-11-28|
    US4128642A|1976-12-20|1978-12-05|International Minerals & Chemical Corp.|Method of promoting growth and improving feed efficiency of animals|
    US4100284A|1977-01-18|1978-07-11|Pfizer Inc.|1,4-Dioxo- and 4-oxoquinoxaline-2-carboxaldehyde sulfonylhydrazones and certain derivatives thereof|
    CS195508B1|1977-08-02|1980-02-29|Jaromir Hebky|Cyanacetylhydrazones of 2-formylquinoxalin-1,4-dioxide|
    US4224324A|1979-05-21|1980-09-23|International Minerals And Chemical Corporation|Nitro-olefin-substituted quinoxaline dioxides|HU184293B|1980-06-03|1984-07-30|Egyt Gyogyszervegyeszeti Gyar|Process for preparing quinoxaline-1,4-dioxide derivatives|
    FR2590575B1|1985-11-25|1988-01-29|Interox Sa|PROCESS FOR THE MANUFACTURE OF OXIDES OF AROMATIC TERTIARY AMINES AND PRODUCTS THUS OBTAINED|
    IE66512B1|1989-02-28|1996-01-10|Ici Plc|Heterocyclic ethers as 5-lipoxygenase inhibitors|
    WO2003032916A2|2001-10-16|2003-04-24|Structural Bioinformatics Inc.|Organosulfur inhibitors of tyrosine phosphatases|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    HU801298A|HU184772B|1980-05-23|1980-05-23|Process for preparing quinoxaline-1,4-dioxide derivatives|
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