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    Phenyl-imidazolyl acetic acid amino alkanol esters and amides
    3.
    发明授权
    Phenyl-imidazolyl acetic acid amino alkanol esters and amides 失效
    苯基咪唑啉酮酸性氨基酸烷基酯和氨基酸

    公开(公告)号：US3872117A

    公开(公告)日：1975-03-18

    申请号：US13928471

    申请日：1971-04-30

    Applicant: BAYER AG

    Inventor： MEISER WERNER ,  METZGER CARL ,  BUCHEL KARL HEINZ ,  PLEMPEL MANFRED

    IPC: C07D233/54 ,  C07D233/56 ,  C07D249/08 ,  C07D521/00 ,  C07D87/42

    CPC classification number: C07D231/12 ,  C07D233/56 ,  C07D249/08

    Abstract: Antimicrobial aminoalkyl phenyl-azolylalkanoates and N(aminoalkyl)phenyl-azolylalkanamides and salts thereof are prepared by treatment of the corresponding phenyl-halo-alkanoate or alkanamide with an azolyl compound or saalt thereof, treatment of the corresponding phenyl-hydroxyalkanoate or phenylhydroxyalkanamide with an azole compound under dehydration conditions or with a thionyl-bis-azole, or transesterification or amidation of a (lower)alkyl phenyl-azolylalkanoate. A typical embodiment is diphenyl-imidazolyl-acetic acid 1-dimethylamino-2propyl ester.

    Abstract translation: 通过用唑基化合物或其盐处理相应的苯基 - 卤代 - 链烷酸酯或烷酰胺，处理相应的苯基 - 羟基链烷酸酯或苯基 - 羟基链烷酰胺来制备抗微生物氨基烷基苯基 - 唑基烷酰胺和N-（氨基烷基）苯基 - 唑基烷酰胺及其盐 在脱水条件下或与亚硫酰基 - 双 - 唑的唑化合物，或（低级）烷基苯基 - 唑基烷酸酯的酯交换或酰胺化。 典型的实施方案是二苯基 - 咪唑基 - 乙酸1-二甲基氨基-2-丙基酯。

    Combating fungi with 1-ethylimidazoles
    4.
    发明授权
    Combating fungi with 1-ethylimidazoles 失效
    抗真菌与1-乙基咪唑

    公开(公告)号：US3914427A

    公开(公告)日：1975-10-21

    申请号：US43888774

    申请日：1974-02-01

    Applicant: BAYER AG

    Inventor： KRAMER WOLFGANG ,  BUCHEL KARL HEINZ ,  MEISER WERNER ,  FROHBERGER PAUL-ERNST ,  SCHEINPFLUG HANS

    IPC: A01N43/50 ,  A01P3/00 ,  C07C45/63 ,  C07C45/75 ,  C07D233/60 ,  C07D521/00 ,  A01N9/22

    CPC classification number: C07D231/12 ,  C07C45/63 ,  C07C45/75 ,  C07D233/56 ,  C07D249/08 ,  C07C49/255

    Abstract: Compositions containing and methods of using 1-ethylimidazoles of the formula

    in which R1 and R3 each individually is hydrogen, alkyl, alkenyl, cycloalkyl, cycloalkenyl, optionally substituted aryl or optionally substituted aralkyl, R2 is alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, optionally substituted aryl or optionally substituted aralkyl, Y is oxygen or sulfur, and X is a keto group or a functional derivative of a keto group, AS SUCH OR IN THE FORM OF SALTS, FOR COMBATING FUNGI.

    Abstract translation: 含有式（I）的1-乙基咪唑的组合物和其中R 1和R 3各自独立地为氢，烷基，烯基，环烷基，环烯基，任选取代的芳基或任选地 取代的芳烷基，R 2是烷基，烯基，炔基，环烷基，环烯基，任选取代的芳基或任选取代的芳烷基，Y是氧或硫，X是酮基或酮基的官能衍生物， 用于组合真菌。

    Herbicidal agents
    5.
    发明授权
    Herbicidal agents 失效
    除草剂

    公开(公告)号：US3671523A

    公开(公告)日：1972-06-20

    申请号：US3671523D

    申请日：1970-01-28

    Applicant: BAYER AG

    Inventor： WESTPHAL KURT ,  MEISER WERNER ,  FUE LUDWIG ,  HACK HELMUTH

    IPC: A01N43/707 ,  C07D253/06 ,  C07D253/075 ,  C07D55/10

    CPC classification number: C07D253/075 ,  A01N43/707 ,  C07D253/06

    Abstract: 3-(HYDROGEN-, (UNSUBSTITUTED AND HALO, AMINO, ALKYLAMINO, NITRO, ALKYL, ALKOXY, ALKYLMERCAPTO, ARYLOXY AND/OR HALOARYLMERCAPTO, SUBSTITUTED) ALIPHATIC-, CYCLOALIPHATIC-, ARALIPHATIC-, ARYL-, OR N-heterocyclic- or O-alkanoyl-, -substituted oxy, mercapto or amino)- 4-(amino; mono and di (unsubstituted and cyano, hydroxy and/or halo, -substituted) alkyl- and/or alkanoyl-, -amino; N(unsubstituted and cycloalkyl, aryl, haloaryl, alkaryl, alkoxy aryl, nitroaryl, halo-nitro-aryl, aryl-alkenyl, heterocyclic and/or nitro- heterocyclic- -substituted) alkylidene-amino or cycloalkylidene- amino; or N-heterocyclic)-6-((unsubstituted and halo, nitro, carbo lower alkoxy, alkyl, alkoxy, aryloxy, alkylmercapto, arylmercapto and/or aralkylmercapto, -substituted) aliphatic, cycloaliphatic, araliphatic, aryl, heterocyclic or heterocyclic- alkyl)-1,2,4-triazine-5-ones, which possess herbicidal properties, and which may be produced by conventional methods; herbicidal compositions containing such compounds; and methods of using such compounds as herbicides.

    Abstract translation: 3- [氢 - ，（不含取代的和HALO，氨基，烷基氨基，NITRO，烷基，烷氧基，烷氧基，芳基和/或HALOARYLMERCAPTO，-SUBSTITUTED）烷基 - ，环烷基 - ，亚氨基 - ，芳基 - 或N-杂环 - O-烷酰基 - 取代的氧基，巯基或氨基] -4- [氨基; 单和二（未取代和氰基，羟基和/或卤素，取代的）烷基 - 和/或烷酰基 - ， - 氨基; N-（未取代的和环烷基，芳基，卤代芳基，烷芳基，烷氧基芳基，硝基芳基，卤代 - 硝基 - 芳基，芳基 - 烯基，杂环和/或硝基 - 杂环 - 取代的）亚烷基 - 氨基或亚环烷基 - 或N-杂环] -6 - [（未取代的和卤素，硝基，碳低级烷氧基，烷基，烷氧基，芳氧基，烷基巯基，芳基巯基和/或芳烷基巯基，取代的）脂族，脂环族，芳脂族，芳基，杂环或杂环烷基 ] -1,2,4-三嗪-5-酮，其具有除草性质，并且可以通过常规方法制备; 含有这些化合物的除草组合物; 以及使用这些化合物作为除草剂的方法。

    Phenyl-imidazolyl-alkanyl derivatives, their production and use
    6.
    发明授权
    Phenyl-imidazolyl-alkanyl derivatives, their production and use 失效
    苯基 - 咪唑烷基 - 烷基衍生物，其生产和使用

    公开(公告)号：US3892764A

    公开(公告)日：1975-07-01

    申请号：US34693973

    申请日：1973-04-02

    Applicant: BAYER AG

    Inventor： METZGER CARL ,  MEISER WERNER ,  BUECHEL KARL HEINZ ,  PLEMPEL MANFRED

    IPC: C07D521/00 ,  C07D49/36

    CPC classification number: C07D231/12 ,  C07D233/56 ,  C07D249/08

    Abstract: Phenyl-imidazolylalkanyl derivatives are antimycotic agents. They are prepared by a number of processes including acylation or sulfonylation of a phenyl-imidazolylalkanol, treatment of a phenyl-alkanyl-carbinol with a diimidazolyl sulfone, oxidation of a phenyl-imidazolylalkylmercaptan or reduction of a phenylimidazolylalkanoate or alkanonitrile. A typical embodiment is 1(1,1-diphenyl-2-acetoxyethyl)imidazole.

    Abstract translation: 苯基 - 咪唑烷基烷基衍生物是抗真菌剂。 它们通过许多方法制备，包括苯基 - 咪唑基烷醇的酰化或磺酰化，用二咪唑基砜处理苯基 - 烷基 - 甲醇，氧化苯基 - 咪唑烷基硫醇或还原苯基 - 咪唑烷基链烷酸酯或链烷腈。 典型的实施方案是1-（1,1-二苯基-2-乙酰氧基乙基）咪唑。

    1-Substituted-1,2,4-triazoles
    9.
    发明授权
    1-Substituted-1,2,4-triazoles 失效
    1-取代的-1,2,4-三唑

    公开(公告)号：US3912752A

    公开(公告)日：1975-10-14

    申请号：US31896372

    申请日：1972-12-27

    Applicant: BAYER AG

    Inventor： MEISER WERNER ,  BUCHEL KARL HEINZ ,  KRAMER WOLFGANG ,  GREWE FERDINAND

    IPC: A01N43/653 ,  A01P3/00 ,  C07C45/63 ,  C07C45/70 ,  C07C49/213 ,  C07D249/08 ,  C07D521/00

    CPC classification number: C07D231/12 ,  C07C45/63 ,  C07C45/70 ,  C07C49/213 ,  C07D233/56 ,  C07D249/08 ,  C07C49/255 ,  C07C49/233

    Abstract: in which X1 represents hydrogen or an alkyl radical, X2 represents hydrogen or an alkyl radical, R1 represents an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, R2 represents hydrogen or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, R3 represents hydrogen or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, and Y represents a keto group or a functional keto derivative, WHICH POSSESS FUNGICIDAL PROPERTIES.
    1-SUBSTITUTED-1,2,4-TRIAZOLES OF THE FORMULA

    Abstract translation: 其中X 1表示氢或烷基，X 2表示氢或烷基，R 1表示烷基，烯基，炔基，R 1表示烷基，链烯基，炔基， ，环烷基，环烯基或任选取代的芳基或芳烷基，R 2表示氢或烷基，烯基，炔基，环烷基，环烯基或任选取代的芳基或芳烷基，R 3表示氢或烷基，烯基，炔基，环烷基，环烯基或任选地 取代的芳基或芳烷基，Y表示酮基或官能酮衍生物，其具有无害的杀真菌性质。

    Imidazolyl ketones for treating mycotic infections
    10.
    发明授权
    Imidazolyl ketones for treating mycotic infections 失效
    用于治疗真菌感染的咪唑啉酮

    公开(公告)号：US3903287A

    公开(公告)日：1975-09-02

    申请号：US40205073

    申请日：1973-10-01

    Applicant: BAYER AG

    Inventor： MEISER WERNER ,  BUCHEL KARL HEINZ ,  PLEMPEL MANFRED

    Abstract: Imidazole derivatives of alkyl, cycloalkyl or aryl ketones are antimycotic agents. The compounds, of which 1-imidazolyl-1-(4''chlorophenoxy)-3,3-dimethylbutan-2-one is a typical embodiment, can be obtained from the corresponding hydroxy or halo ketone through treatment with imidazole.

    Abstract translation: 烷基，环烷基或芳基酮的咪唑衍生物是抗真菌剂。 其中1-咪唑基-1-（4'-氯苯氧基）-3,3-二甲基丁-2-酮的化合物是典型的实施方案，可以通过用咪唑处理从相应的羟基或卤代酮获得。

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