• 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 chemical plant protection products and allows using it as a fungicidal agent for controlling diseases of tomato and grape plants. An increase in fungicidal activity up to 100% at C 100 h / ml in g, b is achieved by using an emulsion concentrate containing the active substance (in wt.%) Of the formula (A) (B) C CR., - CX-e , where A -, BY- (CR CRf), in which R is hydrogen, alkyl Sc,, cyano, and also chlorine or bromine, if k is 0; Rj is hydrogen, amino, nitro, methyl, methoxy, chlorine, bromine; RJ is hydrogen, alkyl, amino, acetamino, halogen, methoxy, trifluoromethyl, hydroxy, difluoromethoxy, RI and Rj together — OCH, 0 or R — hydrogen, hydroxy, amino, methyl, ethyl, butyl, methoxy, propoxy, chlorine, bromine, nitro, allyloxy, dimethylamino, N-methyl, N-butyl-amino, methylthio, trifluoromethyl, difluoromethoxy; R and R, are the same or different and mean hydrogen, methyl; R and Y together mean - (W,) f Y - cyclohexyl, pyridyl, furanyl, naphthyl, 4-methoxy-naphthalen-1-yl, benzyl, cyclopentyl, cyclohexenyl, alkyl C, -C, hexyl, and also methyl, if k means 1 or group, where R, is hydrogen, hydroxy, chlorine, nitro, methyl, methoxy; hydrogen, chlorine, bromine, methyl, nitro, methoxy, trifluoromethyl; Rg is hydrogen, fluorine, chlorine, bromine, amino, nitro, dime-Tylamino, alkyl, methoxy, ethoxy, phenyl, cyclohexyl or Rg and Rg OCHjO; k is 0.1 or 2; X - oxygen, sulfur; Q is the group NR, o R, oN (CH) R, 3 OR, 2 (CH.), (CHCHSNCH; N (CHg) SI ,; N (CH.). Osn (snz); tUcHTTTCH; -S ( CH2) 40, f5 (CH) o, N (CH2), j (C, Hj) 2, where R and R are the same or different mean hydrogen alkyl C, -C, benzyl, allyl or n-dodecyl; R hydrogen, methyl , ethyl, butyl; R, j is hydrogen, methyl, and both radicals A and B do not simultaneously denote phenyl, monohalophenyl, mononitrophenyl mono aminophenyl (0.5), solvent - acetone (98.5), surfactant - tri-n-propylamine salt n-dodecylbenzenesulfonic acid (1.0). 7 table. g U) co with Oi with co
    公开号:SU1336938A3
    申请号:SU853903101
    申请日:1985-06-07
    公开日:1987-09-07
    发明作者:Никкель Йозеф；Пипер Гельмут；Куртце Юрген；Драндаревски Кристо；Луст Зигмунд
    申请人:Целамерк Гмбх Унд Ко,Кг (Фирма)；
    IPC主号:
    专利说明:

    1P369382
    This invention relates to chemical agents.
    KIM means of plant protection, and the names listed in Table 1. Active
    but to the fungicidal agent in the form of a substance the agent is acylated
    emulsion concentrate.
    The purpose of the invention is to increase the fungicidal activity.
    by the addition of appropriately substituted acrylic acid derivatives with carboxylic acid derivatives in the presence of an acid activating or dehydrating agent,
    The invention is illustrated by examples in which, as active
    Derivatives of saturated carboxylic acid A.
    C CI -CO-Q 6
    by the addition of appropriately substituted acrylic acid derivatives with carboxylic acid derivatives in the presence of an acid activating agent or its dehydrating agent,
    Table 1
    Cis / trans isomers 3: 2
    cis / trans 3: 2 trans-isomer
    C1
    C1
    C1
    1JH C1
    , C1

    C1
    Oq
    Qo
    : G.
    140-144
    150-155 168-171
    256-258 165-180
    Table 2 carboxylic acid
    soa
    97 S-CHjA-CH O
    NtCH,)
    0.56
    The analysis of oily products is listed in Table 3.
    The analysis of oily products is given in Table 4.

    70.87 59.72 62.99 79.05 65.03 58.34 75.59 74.75 59.72 74.30 70.98 75.62 65.97 72.42
    70.71 59.87 63.20 78.96 64.74 58.67 75.89 74.55 59.91 74.61 71.06 75.61 65.73 72.54
    Analysis of the products is given in table., 5,
    Table 3
    Table 4

    6.10 5.21 4.67 7.78 5.77 5.25 7.69 7.01 5.12 6.73 6.68 7.35 5.91 7.26
    3.94
    3.32
    3.87
    4.01
    3.61
    3.24
    3.83
    4.15 3, 32
    4.33
    8.28
    3.84
    7.33
    3.67
    4.05 3.17 3.70 3.86 3.60 3.22 3.69 4.17 3.18 4.01 8.16 4.03 7.19 3.50
    Table 5
    eleven
    Continuation of table 6
    1336938
    12 Continuation of table 6
    mopara vlticola.
    21133693822
    Continued tabl.7
    Fungicidal agent in the form of an emulsion — where R is hydrogen, hydroxy, chlorine,
    Zionic concentrate containing ak-nitro, methyl, methoxy;
    A tive substance derived from the non-R-hydrogen, chlorine, bromine, methyl,
    carboxylic acid, soluble nitro, methoxy or trifluorotel and surface active substance methyl
    2313369382D
    Rg is hydrogen, fluorine, chlorine, bromine, fluorine, chlorine, bromine, methyl, amino, nntro, dimethylamino, methoxy, ethoxy.
    amio, nitro, dimethylamino,., - alkyl, methoxy, ethoxy, phenyl or cyclohexyl, or Rg and P, together mean OCHjO,
    k 0.1 or 2;
    X is oxygen or sulfur;
    O. - group of formulas
    5 (U) 0 -NH-Nr) oi
    ten
    15
    Vb / RiZ
    ABOUT
     V-0
    SNS
    -0, X- oxygen, (i is the forp group, py
    liQo or Qo
    RIIsnz
    R, 2 is hydrogen, methyl, ethyl, butyl, R is hydrogen, methyl;
    07.03.83 with Rj and Rj together mean 0-CH2-0, R4 allyloxy, R j- and R j - the same or different methyl, Ry and Y together mean the group - (CH) -, Y - pyridyl, furanyl, naphthyl, C2-C4-alkyl, hexyl, a group of general formula
    where and R is the same or different, hydrogen, alkyl, benzyl, allyl, or n-dodecyl;
     hydrogen, methyl, ethyl, butyl R, - hydrogen, methyl; A and B do not simultaneously mean phenyl, monohalophenyl, mononitrophenyl and monoamine-phenyl,
    acetone is used as a solvent, and n-dodecylbenzenesulfonic acid tri-n-propylamine salt is used as a surfactant in the following proportion of components, (wt.%):
    The compound of General formula (1) 0.5
    Acetone98.5
    Tri-n-propyl amino salt of n-dodecylbenzene sulfonic acid 1.0 Priority on the basis of:
    28, 83 with R, is hydrogen or C -C alkyl, I is hydrogen, alkyl, chlorine, bromine, nitro, methyl, methoxy, amino, RJ is hydrogen, C, -Cj -pakyl, amino, halogen, methoxy, R is hydrogen, hydroxyl, amino, methyl, ethyl, butyl methoxy, propoxy, chlorine, bromine, nitro dimethylamino, M-methyl, N-butylamino, R and R, is hydrogen, Y is a radical of the general formula
    "eight.
    R is hydrogen, chlorine, nitro, methyl, methoxy, Rj is hydrogen, chlorine, bromine, methyl, nitro, methoxy, Rg is hydrogen.

    po, dimethylamino, methoxy, ethoxy.

    -0, X- oxygen, (i is the forp group, py
    liQo or Qo
    RIIsnz
    R, 2 is hydrogen, methyl, ethyl, butyl, R is hydrogen, methyl;
    07.03.83 with Rj and Rj together mean 0-CH2-0, R4 allyloxy, R j- and R j - the same or different methyl, Ry and Y together mean the group - (CH) -, Y - pyridyl, furanyl, naphthyl, C2-C4-alkyl, hexyl, a group of general formula
     R-7
    9
    k 1, R is hydroxy, Q is a group of formulas
    NR-ic H
    HN-T4 (0
    RIO and “11
    - identical or different, hydrogen, -alkyl, benzyl;
    27., 02.84 with R, is cyano, and also chlorine and bromine, if, R is acetates, mino, trifluoromethyl, hydroxyl, difluoromethoxy, R4 methylthio, trifluoromethyl, difluoromethoxy, together mean, Y is cyclohexyl, 4- methoxy-naphthapin-1-yl, benzyl, cyclopentyl, cyclohexenyl, and also methyl, sly, a group of the general formula RT
    go
    9
    where Rg is trifluoromethyl, Nd is 45 alkyl, phenyl, cyclohexyl, Rg and Rg together mean,,, 0. is a group of the formula
    NR, o 11.
    ABOUT

    MO
    and R, aplil, n-dodecyl.
    权利要求:
    Claims (1)
    [1]
    Claim
    A fungicidal agent in the form of an emulsion concentrate containing an active substance derived from an unsaturated carboxylic acid, a solvent and a surfactant, where R - hydrogen, hydroxy, chlorine, nitro, methyl, methoxy;
    R g “hydrogen, chloro, bromo, methyl, nitro, methoxy or trifluoromethyl;
    fluorine, chlorine, bromine, methyl, amino, nit> ro, dimethylamino, methoxy, ethoxy, k = O, X is oxygen, Q is a group of the formula or
    R12
    R, is hydrogen, fluoro, chloro, bromo, amino, nitro, dimethylamino, C 1 -C, alkyl, methoxy, ethoxy, phenyl or cyclohexyl, or Rg and R, together mean OCH g O, k = 0.1 or 2;
    X is oxygen or sulfur;
    Q, is the group of formulas
    F 3
    NR 10 R u -nQ) o> -NH-nQ / 0,
    Riz
    Ή
    Y-o sn 3 R n R 13 A and
    R is the same or different, hydrogen, C 1 -C 4 alkyl, benzyl, allyl, or n-dodecyl;
    hydrogen, methyl, ethyl, butyl; hydrogen, methyl;
    at the same time do not denote phenyl, monohalogenophenyl, mononitrophenyl and monoaminophenyl, acetone as a solvent, and the tri-n-propylamine salt of n-dodecylbenzenesulfonic acid as a surfactant in the following quantitative components (wt.%):
    Compound of the general formula (1) Acetone Tri-n-propylamine salt of n-dodecibenzenesulfonic acid Priority:
    02/28/83 at R, is hydrogen or C 1 ~ C 4 alkyl, Rj is hydrogen, alkyl, chlorine, bromine, nitro, methyl, methoxy, amino, Rj is hydrogen, C, -C 3 -alkyl, amino, halogen, methoxy, R 4 - hydrogen, hydroxyl, amino, methyl, ethyl, butyl, methoxy, propoxy, chlorine, bromine, nitro, dimethylamino, N-methyl, N-butylamino, Rj and - hydrogen, Y - radical of the general formula in the ratio ·
    0.5
    98.5
    1.0 about at
    R - hydrogen, chlorine, nitro, methyl, methoxy, R - hydrogen, chlorine, bromine, methyl, nitro, methoxy, Rg - hydrogen, sn 3 methyl, ethyl, butyl, methyl;
    and R
    R (Z %
    - hydrogen
    - hydrogen
    03/07/83 when R 2 and R 3 together mean O-CH 2 -O, R 4 - allyloxy, R f and R fc - the same or different f methyl, R and Y together mean a group - (CH 2 ) S “, Y - pyridyl, furanyl, naphthyl, C 2 -C 4 -alkyl, hexyl, a group of the general formula k = mule
    1, R-,
    NR R *>
    hydroxy, Q - group form30 HN_N C / ° and R „ R io
    27..02.84 identical or different, hydrogen, C 1 -C 4 -alkyl, benzyl;
    at R, - cyano, as well as chlorine and bromine, if k = 0, R 5 - acetamino, trifluoromethyl, hydroxyl, difluoromethoxy, R 4 - methylthio, trifluoromethyl, difluoromethoxy, R ^ JLR.i together mean 0CH 2 CH, 0, Y is cyclohexyl, 4-methoxynaphthalen-1-yl, benzyl, cyclopentyl, cyclohexenyl, and also methyl, if k = 1, a group of the general formula “A in 9 where R g is trifluoromethyl, Rg is C -C 4 alkyl, phenyl, cyclohexyl, R g and Rg together mean OCH ^ O, k = 2, X = sulfur, Q. is a group of the formula
    NR ( 0 R tt >
    N
    -ABOUT
    -N
    -nQo and R „allyl, n-dodecyl.
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE1222926C2|1960-03-09|1976-07-15|General Aniline & Filme Corporation, New York, N.Y. |PROTECT ORGANIC SUBSTANCES AGAINST UV RADIATION|
    FR1259830A|1960-05-19|1961-04-28|Bayer Ag|Protective filter against ultraviolet rays consisting of a substituted aryl-ethyl product|
    FR4305M|1964-04-06|
    NL295240A|1963-02-05|
    US4342781A|1981-05-29|1982-08-03|Pfizer Inc.|Diphenylpropenamides as SRS-A antagonists|USRE35985E|1983-02-28|1998-12-08|American Cyanamid Company|Fungicidal compositions|
    US5910496A|1984-02-27|1999-06-08|American Cyanamid Company|Fungicidal compositions|
    US4781750A|1985-08-27|1988-11-01|Rohm And Haas Company|Herbicidally active enols|
    EP0219756B1|1985-10-09|1994-01-05|Shell Internationale Researchmaatschappij B.V.|Acrylic amides|
    US5182301A|1986-03-17|1993-01-26|Eisai Co., Ltd.|Diphenylethylene derivatives pharmaceutical compositions containing same and treatment methods|
    FI92189C|1986-03-17|1994-10-10|Eisai Co Ltd|A process for preparing a diphenylmethane derivative useful as a medicament|
    DE3643403A1|1986-12-19|1988-06-30|Shell Agrar Gmbh & Co Kg|BENZOPHENONE AND METHOD FOR THE PRODUCTION THEREOF|
    US5157028A|1987-01-30|1992-10-20|Shell Research Limited|Fungicidal compositions|
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    US5262414A|1987-01-30|1993-11-16|Shell Research Limited|Fungicidal compositions|
    DE3719488A1|1987-06-11|1988-12-29|Shell Agrar Gmbh & Co Kg|METHOD FOR PRODUCING 3,3-DIARYLACRYLIC ACID AMIDES|
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    优先权:
    申请号 | 申请日 | 专利标题
    DE19833306996|DE3306996A1|1983-02-28|1983-02-28|Acrylomorpholides, their preparation and use|
    DE19833308045|DE3308045A1|1983-03-07|1983-03-07|Acrylamides, their preparation and use|
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