专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

1. 发明授权

US07030063B1 Cyclohexenonquinolinoyl-derivatives as herbicidal agents 失效
标题翻译：环己烯醌喹啉基衍生物作为除草剂
公开(公告)号：US07030063B1
公开(公告)日：2006-04-18
申请号：US09763704
申请日：1999-08-27
申请人： Matthias Witschel , Ulf Misslitz , Ernst Baumann , Wolfgang von Deyn , Klaus Langemann , Guido Mayer , Ulf Neidlein , Roland Götz , Norbert Götz , Michael Rack , Stefan Engel , Martina Otten , Karl-Otto Westphalen , Helmut Walter
发明人： Matthias Witschel , Ulf Misslitz , Ernst Baumann , Wolfgang von Deyn , Klaus Langemann , Guido Mayer , Ulf Neidlein , Roland Götz , Norbert Götz , Michael Rack , Stefan Engel , Martina Otten , Karl-Otto Westphalen , Helmut Walter
IPC分类号： A01N43/42 , C07D401/08
CPC分类号： C07D401/06 , A01N43/42 , C07D215/14 , C07D215/18 , C07D215/36 , C07D401/08 , C07D405/12 , C07F9/60
摘要： Cyclohexenonequinolinoyl derivatives of the formula I where: R1 is hydrogen, nitro, halogen, cyano, alkyl, haloalkyl, alkoxyiminomethyl, alkoxy, haloalkoxy, alkylthio, C1–C6-haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, unsubstituted or substituted amino sulfonyl, unsubstituted or substituted sulfonyl amino, unsubstituted or substituted phenoxy, unsubstituted or substituted heterocyclyloxy, unsubstituted or substituted phenylthio or unsubstituted or substituted heterocyclylthio; R2, R3 are hydrogen, alkyl, haloalkyl or halogen; R4 is substituted (3-oxo-1-cyclohexen-2-yl)carbonyl or substituted (1,3-dioxo-2-cyclohexyl)methylidene; and their agriculturally useful salts; processes for preparing the cyclohexenonequinolinoyl derivatives; compositions comprising them, and the use of these derivatives or compositions comprising them for controlling undesirable plants are described.
摘要翻译：式I的环己烯酮喹啉基衍生物其中：R 1是氢，硝基，卤素，氰基，烷基，卤代烷基，烷氧基亚氨基甲基，烷氧基，卤代烷氧基，烷硫基，C 1 -C 未取代或取代的磺酰基氨基，未取代或取代的苯氧基，未取代或取代的杂环氧基，未取代或取代的苯硫基或未取代或取代的杂环硫基; R 2，R 3是氢，烷基，卤代烷基或卤素; R 4是取代的（3-氧代-1-环己烯-2-基）羰基或取代的（1,3-二氧代-2-环己基）亚甲基; 及其农业用盐; 制备环己烯醌喹啉基衍生物的方法; 描述了包含它们的组合物以及包含它们的这些衍生物或组合物用于防治不期望的植物的用途。

2. 发明授权

US06727385B1 Method for producing o-chloromethyl benzoic acid chlorides 失效
标题翻译：邻氯甲基苯甲酸氯化物的生产方法
公开(公告)号：US06727385B1
公开(公告)日：2004-04-27
申请号：US10130825
申请日：2002-08-12
申请人： Roland Götz , Norbert Götz , Michael Keil , Bernd Wolf , Adrian Steinmetz , Armin Stamm , Jochem Henkelmann
发明人： Roland Götz , Norbert Götz , Michael Keil , Bernd Wolf , Adrian Steinmetz , Armin Stamm , Jochem Henkelmann
IPC分类号： C07C5536
CPC分类号： C07C51/60 , C07C63/04 , C07C63/10
摘要： A process for preparing o-chloromethylbenzoyl chlorides of the formula I, in which R1 to R4 can be identical or different and are hydrogen, C1-C4-alkyl, halogen or trifluoromethyl, by reacting benzo-fused lactones of the formula II, in which R1 to R4 are as defined above, with thionyl chloride, which comprises carrying out the reaction in the presence of catalytic amounts of boric acid, boric anhydride, borate, boronic acid or boronic acid esters and catalytic amounts of a quaternary ammonium salt is described.
摘要翻译：制备式I的邻氯甲基苯甲酰氯的方法，其中R 1至R 4可以相同或不同，并且是氢，C 1 -C 4 - 烷基，卤素或三氟甲基，通过使苯并稠合的内酯与其中R 1至R 4如上所定义的式II与亚硫酰氯反应，其包括在催化量的硼酸，硼酸酐，硼酸盐，硼酸或硼酸的存在下进行反应描述了酯和催化量的季铵盐。

3. 发明授权

US06713436B1 1-cycloalkylpyrazolyl-benzoyl derivatives 失效
标题翻译： 1-环烷基吡唑基 - 苯甲酰基衍生物
公开(公告)号：US06713436B1
公开(公告)日：2004-03-30
申请号：US10048949
申请日：2002-02-06
申请人： Ulf Neidlein , Norbert Götz , Ulf Misslitz , Roland Götz , Ernst Baumann , Wolfgang von Deyn , Steffen Kudis , Klaus Langemann , Guido Mayer , Matthias Witschel , Martina Otten , Karl-Otto Westphalen , Helmut Walter
发明人： Ulf Neidlein , Norbert Götz , Ulf Misslitz , Roland Götz , Ernst Baumann , Wolfgang von Deyn , Steffen Kudis , Klaus Langemann , Guido Mayer , Matthias Witschel , Martina Otten , Karl-Otto Westphalen , Helmut Walter
IPC分类号： A01N4380
CPC分类号： C07D413/10
摘要： The present invention relates to 1-cycloalkylpyrazolylbenzoyl derivatives of the formula I wherein all variables are as defined in the specification, their agriculturally useful salts, processes for their preparation, and for the use of these compounds or compositions comprising them, for controlling undesirable plants.
摘要翻译：本发明涉及式I的1-环烷基吡唑基苯甲酰基衍生物，其中所有变量如本说明书中所定义，其农业上有用的盐，其制备方法以及用于这些化合物或包含它们的组合物用于防治不期望的植物。

4. 发明授权

US06441236B1 Method for preparing trion-bis(oxime ether) derivatives andrion-mono and trion-bis(oxime ether) derivatives obtained therewith 有权
标题翻译：制备得到的三 - 双（肟醚）衍生物和单 - 和三 - 双（肟醚）衍生物的方法
公开(公告)号：US06441236B1
公开(公告)日：2002-08-27
申请号：US09787950
申请日：2001-03-23
申请人： Thomas Grote , Bernd Wolf , Michael Rack , Roland Götz , Andreas Gypser , Adrian Steinmetz , Hubert Sauter , Michael Keil , Horst Mayer
发明人： Thomas Grote , Bernd Wolf , Michael Rack , Roland Götz , Andreas Gypser , Adrian Steinmetz , Hubert Sauter , Michael Keil , Horst Mayer
IPC分类号： C07C24900
CPC分类号： C07C251/38 , C07C249/08 , C07D317/28 , C07D319/06
摘要： The present invention relates to a method for the production of trion-bis(oxime ether) derivatives of formula (I), wherein the substituents have the following meaning: R1, R3 represent unsubstituted, partially or totally halogenated C1-C6-alkyl or C3-C6-cycloalkyl; R2, R4 represent C1-C4-alkyl or a methyl substituted by C2-C4-alkenyl, C2-C4-alkinyl or phenyl and X represents oxygen or N—OH. The invention also relates to the intermediate products obtained with said method.
摘要翻译：本发明涉及制备式（I）的三 - 双（肟醚）衍生物的方法，其中取代基具有以下含义：R 1，R 3表示未取代的，部分或全部卤代的C 1 -C 6烷基或C 3 -C 6-环烷基 R 2，R 4表示C 1 -C 4 - 烷基或被C 2 -C 4 - 烯基，C 2 -C 4 - 炔基或苯基取代的甲基，X表示氧或N-OH。本发明还涉及用所述方法获得的中间产物。

5. 发明授权

US06344589B1 Method and intermediate products for producing bis(oxime)monoethers 失效
标题翻译：用于生产双（肟）单醚的方法和中间产物
公开(公告)号：US06344589B1
公开(公告)日：2002-02-05
申请号：US09830970
申请日：2001-05-03
申请人： Wassilios Grammenos , Hubert Sauter , Andreas Gypser , Herbert Bayer , Norbert Götz , Roland Götz
发明人： Wassilios Grammenos , Hubert Sauter , Andreas Gypser , Herbert Bayer , Norbert Götz , Roland Götz
IPC分类号： C07C24900
CPC分类号： C07C249/06 , C07C249/08 , C07C251/40
摘要： A process for preparing bis(oxime) monoethers of the formula I, where: R1 is unsbustituted C1-C4-alkyl or C2-C4-alkenyl-, C2-C4-alkynyl- or phenyl-substituted methyl; R2,R4 independently of one another are hydrogen or methyl; R3,R5 independently of one another are hydrogen or C1-C4-alkyl, trifluoromethyl or phenyl, and intermediates which are obtainable by this process are described.
摘要翻译：制备式I的双（肟）单醚的方法，其中：R1是未取代的C1-C4-烷基或C2-C4-烯基 - ，C2-C4-炔基或苯基取代的甲基; R2，R4独立地为一另一个是氢或甲基; R 3，R 5彼此独立地是氢或C 1 -C 4 - 烷基，三氟甲基或苯基，以及可通过该方法获得的中间体。

6. 发明授权

US06329359B1 Substituted benzyl oximino compounds 失效
标题翻译：取代的苄基肟基化合物
公开(公告)号：US06329359B1
公开(公告)日：2001-12-11
申请号：US09402878
申请日：1999-10-13
申请人： Wassilios Grammenos , Hubert Sauter , Herbert Bayer , Thomas Grote , Andreas Gypser , Reinhard Kirstgen , Bernd Müller , Arne Ptock , Franz Röhl , Roland Götz , Gisela Lorenz , Eberhard Ammermann , Siegfried Strathmann , Volker Harries
发明人： Wassilios Grammenos , Hubert Sauter , Herbert Bayer , Thomas Grote , Andreas Gypser , Reinhard Kirstgen , Bernd Müller , Arne Ptock , Franz Röhl , Roland Götz , Gisela Lorenz , Eberhard Ammermann , Siegfried Strathmann , Volker Harries
IPC分类号： A61K3115
CPC分类号： C07D203/08 , A01N37/50 , A01N43/20 , C07C251/60 , C07C255/64 , C07C2601/02 , C07D303/36
摘要： The present invention relates to benzyloxyimino compounds of the formula I, where: R1 to R4, X, Y, and Z are as defined in the specification.
摘要翻译：本发明涉及式I的苄氧基亚氨基化合物，其中：R1至R4，X，Y和Z如说明书中所定义。

7. 发明授权

US06187816B1 Phenylketiminooxybenzyl compounds, method for the production and use thereof 失效
标题翻译：苯基亚甲氧基苄基化合物，其制备方法和用途
公开(公告)号：US06187816B1
公开(公告)日：2001-02-13
申请号：US09381048
申请日：1999-09-14
申请人： Wassilios Grammenos , Hubert Sauter , Herbert Bayer , Thomas Grote , Andreas Gypser , Reinhard Kirstgen , Bernd Müller , Arne Ptock , Franz Röhl , Roland Götz , Gisela Lorenz , Eberhard Ammermann , Siegfried Strathmann , Volker Harries
发明人： Wassilios Grammenos , Hubert Sauter , Herbert Bayer , Thomas Grote , Andreas Gypser , Reinhard Kirstgen , Bernd Müller , Arne Ptock , Franz Röhl , Roland Götz , Gisela Lorenz , Eberhard Ammermann , Siegfried Strathmann , Volker Harries
IPC分类号： A01N3700
CPC分类号： C07C251/60 , A01N37/50
摘要： Phenylketiminooxybenzyl compounds of the general formula I where: X is O or NH; R1 is fluorine, chlorine, alkyl, haloalkyl, alkoxy and haloalkoxy; R2 is halogen, alkyl, haloalkyl and alkoxy; R3 is halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, cycloalkyl, unsubstituted or substituted phenyl, unsubstituted or substituted phenoxy or CRa═NORb (Ra=hydrogen or alkyl; Rb=alkyl, alkenyl or alkynyl); n is 1, 2 or 3, and salts thereof, processes for their preparation and their use for controlling animal pests and harmful fungi.
摘要翻译：苯基亚甲氧基苄基化合物，其通式为：其中X为O或NH; R 1为氟，氯，烷基，卤代烷基，烷氧基和卤代烷氧基; R 2为卤素，烷基，卤代烷基和烷氧基; R 3为卤素，烷基，卤代烷基，烷氧基，卤代烷氧基，环烷基，未取代或取代的苯基，未取代或取代的苯氧基或CR a = NORb（R a =氢或烷基; R b =烷基，烯基或炔基）; n为1,2或3及其盐，其制备方法及其用途用于控制动物害虫和有害真菌。

8. 发明授权

US07056941B1 2-[pyrazolyl and triazolyl-3′-oxymethylene]-phenyl-isoxazolones, triazolones and tetrazolones as pesticides and fungicides 失效
标题翻译： 2- [吡唑基和三唑基-3'-氧亚甲基] - 苯基 - 异恶唑酮，三唑酮和四唑酮作为农药和杀真菌剂
公开(公告)号：US07056941B1
公开(公告)日：2006-06-06
申请号：US09462647
申请日：1998-07-02
申请人： Bernd Müller , Hubert Sauter , Herbert Bayer , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Andreas Gypser , Arne Ptock , Reinhard Kirstgen , Norbert Götz , Roland Götz , Franz Röhl , Eberhard Ammermann , Volker Harries , Gisela Lorenz , Siegfried Strathmann
发明人： Bernd Müller , Hubert Sauter , Herbert Bayer , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Andreas Gypser , Arne Ptock , Reinhard Kirstgen , Norbert Götz , Roland Götz , Franz Röhl , Eberhard Ammermann , Volker Harries , Gisela Lorenz , Siegfried Strathmann
IPC分类号： A01N43/653 , C07D249/12
CPC分类号： A01N43/80 , A01N43/653 , C07D249/12
摘要： 2-[Pyrazolyl- and triazolyl-3′-oxymethylene]phenylisoxazolones, -triazolones and -tetrazolones of formula I where: X is a group A, B or C, where # denotes the bond with the phenyl ring, Ra is hydrogen, halogen, alkyl or alkoxy, Rb is alkyl; Y is N or CRc, where Rc is hydrogen, halogen or alkyl; n is 0, 1, 2, 3 or 4, where the substituents R1 may be different if n is greater than 1; R1 is nitro, cyano, halogen, alkyl with or without substitution or alkoxy with or without substitution or is additionally, if n is 2, an optionally substituted 3 or 4 membered bridge which forms together with the ring to which it is attached a bicyclic partially unsaturated or aromatic radical; R2 is hydrogen, nitro, cyano, halogen, alkyl, haloalkyl, alkoxy, alkylthio or alkoxycarbonyl; R3 is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl or optionally substituted hetaryl, their preparation and their use for controlling unwanted animal pests or harmful fungi.
摘要翻译： 2- [吡唑基 - 和三唑基-3'-甲醛]苯基异恶唑酮，式I的三唑酮和四唑酮其中：X是A，B或C基团，其中＃表示与苯环的键，R a 氢，卤素，烷基或烷氧基，R b是烷基; Y是N或CR，其中R c是氢，卤素或烷基; n为0,1,2,3或4，其中如果n大于1，则取代基R 1可以不同; R 1是硝基，氰基，卤素，具有或不具有取代的烷基或具有或不具有取代的烷氧基，或者另外，如果n是2，则与环一起形成的任选取代的3或4元桥其连接有双环部分不饱和或芳族基团; R 2是氢，硝基，氰基，卤素，烷基，卤代烷基，烷氧基，烷硫基或烷氧基羰基; R 3是任选取代的烷基，任选取代的环烷基，任选取代的芳基或任选取代的杂芳基，它们的制备及其用于防治有害动物害虫或有害真菌的用途。

9. 发明授权

US07034181B1 Method for producing o-chloromethyl benzoic acid chlorides 失效
标题翻译：邻氯甲基苯甲酸氯化物的生产方法
公开(公告)号：US07034181B1
公开(公告)日：2006-04-25
申请号：US10130821
申请日：2000-11-27
申请人： Roland Götz , Norbert Götz , Michael Keil , Bernd Wolf , Adrian Steinmetz , Armin Stamm , Jochem Henkelmann
发明人： Roland Götz , Norbert Götz , Michael Keil , Bernd Wolf , Adrian Steinmetz , Armin Stamm , Jochem Henkelmann
IPC分类号： C07C51/58
CPC分类号： C07C51/60 , C07C63/10
摘要： The invention relates to a method for producing o-chloromethyl benzoic acid chlorides of formula (I), in which R1 to R4 can be the same or different and represent hydrogen C1–C4 alkyl, halogen or trifluoromethyl, by reaction benzo condensed lactones of formula (II), in which R1 to R4 have the above-mentioned meaning, with thionyl chloride. The inventive method is characterized in that the reaction is carried out in the presence of catalytic quantities of a Lewis acid and in the presence of catalytic quantities of a phosphine derivative.
摘要翻译：本发明涉及一种制备式（I）的邻氯甲基苯甲酰氯的方法，其中R 1至R 4可以相同或不同，表示氢 C 1 -C 4烷基，卤素或三氟甲基，通过反应式（II）的苯并稠合内酯，其中R 1至R 4， SUP> 4 具有上述含义，与亚硫酰氯。本发明的方法的特征在于反应在催化量的路易斯酸存在下和在催化量的膦衍生物的存在下进行。

10. 发明授权

US06472538B1 Method for producing 1-substituted 5-hydroxypyrazoles 失效
标题翻译： 1-取代的5-羟基吡唑的制备方法
公开(公告)号：US06472538B1
公开(公告)日：2002-10-29
申请号：US09830350
申请日：2001-04-25
申请人： Norbert Götz , Roland Götz , Michael Rack
发明人： Norbert Götz , Roland Götz , Michael Rack
IPC分类号： C07D23120
CPC分类号： C07C243/30 , C07D231/20
摘要： A process for preparing compounds of the formula I in which R1 is hydrogen, an aliphatic group having 1-8 carbon atoms, C1-C6-alkoxycarbonyl, C1-C6-alkylthiocarbonyl or a cyclic ring system having 3-14 ring atoms, and R2 is hydrogen, an aliphatic group having 1-8 carbon atoms, or R1 and R2 together with the carbon atom to which they are bound form a cyclic or bicyclic ring system having 3-14 ring atoms, comprises the preparation of compounds of the formula II in which R3 and R4 are readily detachable groups and R1 and R2 are as defined above, as starting materials or intermediates and the cyclization of these under suitable reaction conditions to give compounds of the formula I.
摘要翻译：制备式Iin的化合物的方法，其中R 1是氢，具有1-8个碳原子的脂族基团，C 1 -C 6烷氧基羰基，C 1 -C 6烷硫基羰基或具有3-14个环原子的环状体系，R 2是氢，具有1-8个碳原子的脂族基团，或R 1和R 2与它们所连接的碳原子一起形成具有3-14个环原子的环状或双环体系，包括制备式II化合物，其中R 3 并且R 4是容易拆分的基团，并且R 1和R 2如上所定义，作为原料或中间体，并在合适的反应条件下环化，得到式I化合物。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式