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1. 发明申请

US20080153824A1 Method for Controlling Fungal Diseases in Leguminous Plants 审中-公开
标题翻译：豆科植物真菌病防治方法
公开(公告)号：US20080153824A1
公开(公告)日：2008-06-26
申请号：US11793617
申请日：2005-12-16
申请人： John-Bryan Speakman , Reinhard Stierl , Siegfried Strathmann , Peter Dombo , Matthias Niedenbruck , Egon Haden , Dirk Voeste , Ulf Groeger
发明人： John-Bryan Speakman , Reinhard Stierl , Siegfried Strathmann , Peter Dombo , Matthias Niedenbruck , Egon Haden , Dirk Voeste , Ulf Groeger
IPC分类号： A01N37/50 , A01N43/653 , A01P3/00 , A01N43/50 , A01N43/56 , A01N43/54 , A01N43/34 , A01N43/36 , A01N43/84 , A01N47/28 , A01N37/00
CPC分类号： A01N37/50 , A01N2300/00
摘要： Method for controlling rust infections in leguminous plants by using orysastrobin, mixtures of orysastrobin and a fungicidally active compound II from the group of the azoles, acylalanines, amine derivatives, anilinopyrimidines, dicarboximides, dithiocarbamates, heterocylic compounds, phenylpyrroles, cinnamides, and analogs, or other fungicides according to the description, and also compositions and seed comprising these mixtures.
摘要翻译：通过使用orysastrobin来控制豆科植物中的生锈感染的方法，或者来自唑烷类的混合物和来自唑类，酰基丙氨酸，胺衍生物，苯胺基嘧啶，二甲酰亚胺，二硫代氨基甲酸酯，杂环化合物，苯基吡咯，肉桂酸酯和类似物的混合物，或根据描述的其它杀真菌剂，以及包含这些混合物的组合物和种子。

2. 发明申请

US20080039320A1 Use Of Menadione 审中-公开
公开(公告)号：US20080039320A1
公开(公告)日：2008-02-14
申请号：US11791464
申请日：2005-11-24
申请人： Harald Kohle , Reinhard Stierl , Randall Gold , Felix Gorth , John-Bryan Speakman , Peter Dombo , Martin Semar , Dieter Strobel , Matthias Niedenbruck , Hans Bestman
发明人： Harald Kohle , Reinhard Stierl , Randall Gold , Felix Gorth , John-Bryan Speakman , Peter Dombo , Martin Semar , Dieter Strobel , Matthias Niedenbruck , Hans Bestman
IPC分类号： A01N35/06 , A01C1/06 , A01N43/40 , A01N43/56 , A01N43/84 , A01P3/00 , A01N43/653 , A01N43/50 , A01N25/00
CPC分类号： A01N35/06 , A01N2300/00
摘要： The use of menadione or one of its plant-compatible acid addition salts for enhancing the activity of agrochemicals against phytopathogenic fungi, mixtures of menadione and at least one active compound selected from the following groups: A) azoles, such as cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, hexaconazole, imazalil, metconazole, myclobutanil, penconazole, prochloraz, prothioconazole, tebuconazole, triadimefon, triadimenol, triflumizole; B) strobilurins, such as azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin or trifloxystrobin; C) acylalanines, such as benalaxyl, metalaxyl, mefenoxam, ofurace, oxadixyl; D) amine derivatives, such as spiroxamine; E) anilinopyrimidines, such as pyrimethanil, mepanipyrim or cyprodinil; F) dicarboximides, such as iprodione, procymidone, vinclozolin; G) cinnamides and analogs, such as dimethomorph, flumetover or flumorph; H) dithiocarbamates, such as ferbam, nabam, maneb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb; I) heterocylic compounds, such as benomyl, boscalid, carbendazim, dithianon, famoxadone, fenamidone, picobenzamid, proquinazid, quinoxyfen, thiophanate-methyl, triforine, 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine, N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)-[1,2,4]triazole-1-sulfonamide or thiophene derivatives of the formula II; K) sulfur and copper fungicides, such as Bordeaux mixture, copper acetate, copper oxychloride, basic copper sulfate; L) nitrophenyl derivatives, such as dinocap; M) phenylpyrroles, such as fenpiclonil or fludioxonil; N) sulfenic acid derivatives, such as captafol, dichlofluanid, tolylfluanid; 0) other fungicides selected from the group consisting of benthiavalicarb, chlorothalonil, cyflufenamid, diclofluanid, diethofencarb, ethaboxam, fenhexamid, fluazinam, iprovalicarb, metrafenone, zoxamide; oxime ether derivatives of the formula III, phenylamidine derivatives of the formula IV, compounds of the formula V, where in the formulae III to V the substituents are defined according to the description; in a synergistically effective amount, methods for controlling harmful fungi using mixtures of menadione with active compounds from groups A) to O) and compositions comprising these mixtures.

3. 发明申请

US20070259919A1 2-Substituted Pyridines, Processes for their Preparation and Their Use for Controlling Harmful Fungi 失效
标题翻译： 2-取代吡啶类，其制备方法及其用于控制有害真菌的应用
公开(公告)号：US20070259919A1
公开(公告)日：2007-11-08
申请号：US11630569
申请日：2005-06-18
申请人： Joachim Rheinheimer , Frank Schieweck , Thomas Grote , Carsten Blettner , Anja Schwogler , Markus Gewehr , Wassilios Grammenos , Udo Hunger , Bernd Muller , Peter Schafer , John-Bryan Speakman , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Joachim Rheinheimer , Frank Schieweck , Thomas Grote , Carsten Blettner , Anja Schwogler , Markus Gewehr , Wassilios Grammenos , Udo Hunger , Bernd Muller , Peter Schafer , John-Bryan Speakman , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A01N43/40 , A01N43/86 , A01P3/00 , C07D213/22 , C07D401/04 , C07D417/04
CPC分类号： C07D401/04 , A01N43/40 , A01N43/54 , A01N43/56 , A01N43/653 , A01N43/78 , C07D213/61 , C07D213/70 , C07D213/74 , C07D213/78 , C07D213/84 , C07D213/86 , C07D417/04
摘要： The invention relates to 2-substituted pyridines of the formula I in which the index n and the substituents R1 to R4 and L are as defined in the description and in each case one of the two ring members X1, X2 is N, the other is C—H or C-halogen; Y is a group —CH—R1—, —N—R1—, —O— or —S— and is five- or six-membered hetaryl comprising 1 to 3 heteroatoms selected from the group consisting of O, N and S or is phenyl, and to processes for their preparation, intermediates for their preparation, pesticidal compositions and methods for controlling harmful fungi and animal pests using the compounds according to the invention.
摘要翻译：本发明涉及式I中的2-取代吡啶，其中指数n和取代基R 1至R 4和L如说明书和每一个中所定义两个环成员X 1，X 2中的一个是N，另一个是CH或C-卤素; Y是基团-CH-R 1 - ，-NR 1 - ， - O-或-S-，并且是包含1至3个的五元或六元杂芳基选自O，N和S的杂原子或为苯基，并且其制备方法，其制备中间体，杀虫组合物和使用本发明化合物控制有害真菌和动物害虫的方法。

4. 发明申请

US20080076785A1 7-Aminomethyl-1,2,4-Triazolo[1,5-A]Pyrimidine Compounds And Their Use For Controlling Pathogenic Fungi 审中-公开
标题翻译： 7-氨基甲基-1,2,4-三唑并[1,5-A]嘧啶化合物及其用于控制致病真菌
公开(公告)号：US20080076785A1
公开(公告)日：2008-03-27
申请号：US11663982
申请日：2005-09-27
申请人： Carsten Blettner , Jordi Tormo i Blasco , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , John-Bryan Speakman , Thorsten Jabs , Siegfried Strathmann , Ulrich Schofl , Maria Scherer , Reinhard Stierl
发明人： Carsten Blettner , Jordi Tormo i Blasco , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , John-Bryan Speakman , Thorsten Jabs , Siegfried Strathmann , Ulrich Schofl , Maria Scherer , Reinhard Stierl
IPC分类号： A01N43/54 , A01P3/00 , C07D239/70
CPC分类号： A01N43/90 , C07D487/04
摘要： The invention relates to 7-aminomethyl-1,2,4-triazolo[1,5-a]pyrimidine compounds of general formula (I) and the agriculturally compatible salts of said compounds. In said formula: R1 and R2 represent hydrogen, alkyl, haloalkyl, alkoxy, cycloalkyl, bicycloalkyl, halocycloalkyl, alkenyl, alkadienyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a 5- or 6-membered saturated, partially unsaturated or aromatic heterocycle, containing 1 to 4 heteroatoms from the group containing O, N or S, or R1 and R2, together with the nitrogen atom to which they are bonded, can also form a five- or six-membered heterocyclyl or heteroaryl, which is bonded by means of N and can contain 1 to 3 additional heteroatoms from the group containing O, N and S as the ring member and can be substituted according to the description; R3 and R4 represent hydrogen, alkyl, haloalkyl, haloalkoxy, alkoxy, or alkoxyalkyl; X represents halogen, cyano, a 5- or 6-membered saturated, partially unsaturated or aromatic heterocycle, containing 1, 2 or 3 heteroatoms from the group containing O, N or S as the ring member, alkyl, alkoxy, alkenyl or alkynyl, whereby the latter 4 groups can be substituted according to the description; L is defined as cited in the claims and the description; and m represents 0, 1, 2, 3, 4 or 5. The invention also relates to the use of the triazolopyrimidine compounds of general formula (I) and their agriculturally compatible salts for controlling plant-pathogenic fungi, to a method for controlling plant-pathogenic fungi, containing at least one compound of general formula (I) and/or an agriculturally compatible salt of said compound and at least one liquid or solid carrier.
摘要翻译：本发明涉及通式（I）的7-氨基甲基-1,2,4-三唑并[1,5-a]嘧啶化合物和所述化合物的农业上相容的盐。在所述式中：R 1和R 2表示氢，烷基，卤代烷基，烷氧基，环烷基，二环烷基，卤代环烷基，烯基，链烯基，卤代烯基，环烯基，卤代环烯基，炔基，卤代炔基或苯基，萘基或5-或6-元饱和，部分不饱和或芳族杂环，含有1至4个含有O，N或S的杂原子，或R 1和R 2与它们所键合的氮原子一起也可以形成五元或六元杂环基或杂芳基，其通过N键合并且可以含有来自含有O，N和S的基团的1至3个另外的杂原子作为环成员，并且可以根据描述进行取代; R3和R4代表氢，烷基，卤代烷基，卤代烷氧基，烷氧基或烷氧基烷基; X代表卤素，氰基，含有1,2或3个杂原子的5-或6-元饱和的部分不饱和或芳族杂环，所述杂环含有作为环成员的O，N或S，烷基，烷氧基，烯基或炔基，由此后4个组可以根据描述被替代; L定义为权利要求书和说明书中引用的; 和m表示0,1,2,3,4或5.本发明还涉及通式（I）的三唑并嘧啶化合物及其农业上相容的盐用于控制植物致病真菌的用途，用于控制植物的方法致病真菌，含有至少一种通式（I）的化合物和/或所述化合物的农业上相容的盐和至少一种液体或固体载体。

5. 发明申请

US20070270311A1 6-Phenyl-7-Aminotriazolopyrimidines, Processes For Their Preparation And Their Use For Controlling Harmful Fungi, And Also Compositions Comprising Them 审中-公开
公开(公告)号：US20070270311A1
公开(公告)日：2007-11-22
申请号：US11661566
申请日：2005-09-02
申请人： Carsten Blettner , Jordi Blasco , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Jochen Dietz , John-Bryan Speakman , Thorsten Jabs , Siegfried Strathmann , Ulrich Schofl , Maria Scherer , Reinhard Stierl
发明人： Carsten Blettner , Jordi Blasco , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Jochen Dietz , John-Bryan Speakman , Thorsten Jabs , Siegfried Strathmann , Ulrich Schofl , Maria Scherer , Reinhard Stierl
IPC分类号： A01N43/90 , A01P3/00 , C07D487/02
CPC分类号： A01N43/90 , A01N47/06 , A01N47/12 , A01N47/16 , C07D487/04
摘要： 6-Phenyl-7-aminotriazolopyrimidines of the formula I in which the substituents are as defined below: R1 is hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle, which comprises one to four heteroatoms from the group consisting of O, N and S, R2 is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which comprises one to four heteroatoms from the group consisting of O, N and S, R3,R4,R5,R6,R7 are hydrogen or one of the groups mentioned under R2, R4, together with R3 or R6, may also form a five- or six-membered saturated or unsaturated ring which, in addition to carbon atoms, may comprise one to three further heteroatoms from the group consisting of O, N and S as ring members; R2 with R3, R4 with R5, R6 with R7 may in each case together, with formation of spiro groups, also form a C2-C5-alkylene, or alkenylene or alkynylene chain which may be interrupted by one to three heteroatoms from the group consisting of O, N and S; p is zero or 1; L is halogen, alkyl, haloalkyl, alkoxy, cyano, nitro, amino, alkylamino, dialkylamino, alkylcarbonylamino, C(O)—R, S(O)n—R; where n is zero, 1 or 2; R is hydrogen, alkyl, haloalkyl, alkoxy, alkenyloxy, alkynyloxy, amino, alkylamino, dialkylamino; m is 1, 2, 3, 4 or 5; X is halogen, cyano, alkyl, alkoxy, alkenyloxy, alkynyloxy or haloalkoxy; Y is oxygen or sulfur; Z is hydrogen, alkyl, haloalkyl, cycloalkyl, alkylcarbonyl, cycloalkylcarbonyl, alkenyl, haloalkenyl, cycloalkenyl, alkynyl, haloalkynyl, phenyl, naphthyl, a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which comprises one to four heteroatoms from the group consisting of O, N and S; or Z together with R4 or R6 may also form a five- or six-membered saturated or unsaturated ring which, in addition to carbon atoms and Y, may comprise one or two further heteroatoms from the group consisting of O, N and S as ring members the groups R1 to R7, Z and R may be substituted according to the description; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.

6. 发明申请

US20060258685A1 Substituted pyrazolopyrimidines, methods for the production thereof, use of the same for controlling pathogenic fungi, and agents containing said compounds 审中-公开
公开(公告)号：US20060258685A1
公开(公告)日：2006-11-16
申请号：US10558251
申请日：2004-05-27
申请人： Olivier Wagner , Thomas Grote , Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Andreas Gypser , Bernd Muller , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Jordi Blasco , Alan Akers , John-Bryan Speakman , Michael Rack , Reinhard Stierl , Maria Scherer , Ulrich Schofl , Siegfried Strathmann
发明人： Olivier Wagner , Thomas Grote , Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Andreas Gypser , Bernd Muller , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Jordi Blasco , Alan Akers , John-Bryan Speakman , Michael Rack , Reinhard Stierl , Maria Scherer , Ulrich Schofl , Siegfried Strathmann
IPC分类号： A61K31/519 , C07D487/04
CPC分类号： C07D487/04 , A01N43/90
摘要： The invention relates to substituted pyrazolopyrimidines of formula (I) wherein the substituents have the following designations: L represents halogen, alkyl, halogenalkyl, alkenyl, alkoxy, amino, NHR, NR2, cyano, S(═O)nA1 or C(═O)A2, R representing alkyl or alkylcarbonyl, A1 representing hydrogen, hydroxy, alkyl, alkylamino or dialkylamino, n representing 0, 1 or 2, and A2 representing alkenyl, alkoxy, halogenalkoxy or one of the groups cited for A1; m represents 0 or 1 to 5; R1 represents alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, alkadienyl, halogenalkenyl, cycloalkenyl, alkinyl, halogenalkinyl or cycloalkinyl, phenyl, naphthyl, or a five-membered to ten-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group O, N or S; and R2 represents hydrogen or one of the groups cited for R1. Together with the nitrogen atom to which they are bonded, R1 and R2 can form a five-membered to six-membered ring that can be interrupted by an atom from the groups O, N and S, and R1 and/or R2 can also be substituted according to the description. Furthermore, in formula (I): X represents halogen, cyano, OH, alkyl, alkoxy or halogenalkoxy; Y represents a five-membered to ten-membered saturated, partially unsaturated or aromatic heterocycle according to the description, or a group X or another group according to the description; p represents 1 or 2, the groups Y being potentially different when p=2; and p represents 0, when X is according to the description. The invention also relates to methods and intermediate products for producing said compounds, agents containing the same, and the use thereof for controlling phytopathogenic fungi.

7. 发明申请

US20060160811A1 Aryl-condensed 3-arylpridine compounds and use thereof for controlling pathogenic fungi 审中-公开
公开(公告)号：US20060160811A1
公开(公告)日：2006-07-20
申请号：US10563222
申请日：2004-07-15
申请人： Oliver Wagner , Thomas Grote , Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Andreas Gypser , Bernd Muller , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Jordi Blasco , Alan Akers , John-Bryan Speakman , Michael Rack , Reinhard Stierl , Maria Scherer , Siegfried Strathmann , Ulrich Schofl
发明人： Oliver Wagner , Thomas Grote , Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Andreas Gypser , Bernd Muller , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Jordi Blasco , Alan Akers , John-Bryan Speakman , Michael Rack , Reinhard Stierl , Maria Scherer , Siegfried Strathmann , Ulrich Schofl
IPC分类号： C07D487/02 , C07D471/02 , A61K31/53 , A61K31/519
CPC分类号： C07D471/04 , A01N43/90
摘要： The present invention relates to bicyclic compounds of general formula I, in which X, Y independently of one another are N or C—R4; n is 1, 2, 3, 4 or 5; Ra is halogen, cyano, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-haloalkyl, C1-C6-haloalkoxy, C2-C6-alkenyl, C2-C6-alkenyloxy or C(O)R5; R1 is halogen, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl which is optionally mono- or polysubstituted by alkyl and/or halogen, C5-C8-cycloalkenyl which is optionally mono- or polysubstituted by alkyl and/or halogen, OR6, SR6 or NR7R8; R2 is halogen, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl which is optionally mono- or polysubstituted by alkyl and/or halogen, C5-C8-cycloalkenyl which is optionally mono- or polysubstituted by alkyl and/or halogen, OR6, SR6 or NR7R8; R3 is hydrogen, C1-C6-alkyl, C1-C6-haloalkyl or C3-C6-cycloalkyl which is optionally mono- or polysubstituted by alkyl and/or halogen; and the agriculturally acceptable salts of compounds I, plant protection agents, containing at least one compound of general formula I and/or one agriculturally-acceptable salt of I and at least one liquid or solid carrier substance, as well as a method for controlling phytopathogenic fungi.

8. 发明授权

US07695728B2 2-substituted pyridines, processes for their preparation and their use for controlling harmful fungi 失效
标题翻译： 2-取代的吡啶，其制备方法及其用于控制有害真菌的用途
公开(公告)号：US07695728B2
公开(公告)日：2010-04-13
申请号：US11630569
申请日：2005-06-18
申请人： Joachim Rheinheimer , Frank Schieweck , Thomas Grote , Carsten Blettner , Anja Schwögler , Markus Gewehr , Wassilios Grammenos , Udo Hünger , Bernd Müller , Peter Schäfer , John-Bryan Speakman , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
发明人： Joachim Rheinheimer , Frank Schieweck , Thomas Grote , Carsten Blettner , Anja Schwögler , Markus Gewehr , Wassilios Grammenos , Udo Hünger , Bernd Müller , Peter Schäfer , John-Bryan Speakman , Maria Scherer , Siegfried Strathmann , Ulrich Schöfl , Reinhard Stierl
IPC分类号： C07D401/04 , C07D213/61 , C07D417/04 , C07D213/70 , C07D213/86 , C07D213/78 , A01N43/40
CPC分类号： C07D401/04 , A01N43/40 , A01N43/54 , A01N43/56 , A01N43/653 , A01N43/78 , C07D213/61 , C07D213/70 , C07D213/74 , C07D213/78 , C07D213/84 , C07D213/86 , C07D417/04
摘要： The invention relates to 2-substituted pyridines of the formula I in which the index n and the substituents R1 to R4 and L are as defined in the description and in each case one of the two ring members X1, X2 is N, the other is C—H or C-halogen; Y is a group —CH—R1—, —N—R1—, —O— or —S— and is five- or six-membered hetaryl comprising 1 to 3 heteroatoms selected from the group consisting of O, N and S or is phenyl, and to processes for their preparation, intermediates for their preparation, pesticidal compositions and methods for controlling harmful fungi and animal pests using the compounds according to the invention.
摘要翻译：本发明涉及式I中的2-取代吡啶，其中指数n和取代基R 1至R 4和L如说明书中所定义，并且在每种情况下，两个环成员X1，X2中的一个为N，另一个为 C-H或C-卤素; Y是基团-CH-R 1，-N-R 1，-O-或-S-，是包含1至3个选自O，N和S的杂原子的五元或六元杂芳基，或者是苯基，及其制备方法，其制备中间体，杀虫组合物和使用本发明化合物控制有害真菌和动物害虫的方法。

9. 发明申请

US20080132522A1 2-Substituted Pyrimidines, Method for Their Production and Their Use for Controlling Pathogenic Fungi 审中-公开
标题翻译： 2-取代嘧啶，其生产方法及其用于控制病原真菌
公开(公告)号：US20080132522A1
公开(公告)日：2008-06-05
申请号：US11631006
申请日：2005-07-12
申请人： Joachim Rheinheimer , Frank Schieweck , Thomas Grote , Carsten Blettner , Anja Schwogler , Markus Gewehr , Wassilios Grammenos , Udo Hunger , Bernd Muller , Peter Schafer , Jochen Dietz , John-Bryan Speakman , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Joachim Rheinheimer , Frank Schieweck , Thomas Grote , Carsten Blettner , Anja Schwogler , Markus Gewehr , Wassilios Grammenos , Udo Hunger , Bernd Muller , Peter Schafer , Jochen Dietz , John-Bryan Speakman , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A01N43/54 , C07D401/04 , A01P3/00 , A01P13/00 , A01P15/00
CPC分类号： C07D239/34 , C07D401/04 , C07D403/12
摘要： The invention relates to 2-substituted pyrimidines of the formula I in which the index n and the substituents R1 to R4, B and L are as defined in the description and Y is a group —O— or —S—, and to processes for their preparation, pesticidal compositions and methods for controlling harmful fungi and animal pests using the compounds according to the invention.
摘要翻译：本发明涉及式I的2-取代嘧啶，其中指数n和取代基R 1至R 4，B和L如说明书中所定义，以及 Y是基团-O-或-S-，并且使用本发明的化合物进行制备，杀虫组合物和控制有害真菌和动物害虫的方法。

10. 发明申请

US20080032889A1 6-(2-Fluorophenyl)-Triazolopyrimidines, Method For The Production Thereof, Use Thereof For Controlling Harmful Fungi, And Agents Containing The Same 审中-公开
标题翻译： 6-（2-氟苯基） - 三唑并嘧啶，其生产方法，用于控制有害真菌及其含有药剂
公开(公告)号：US20080032889A1
公开(公告)日：2008-02-07
申请号：US11630558
申请日：2005-06-14
申请人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bernd Muller , Matthias Niedenbruck , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Barbara Nave , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A01N43/90 , A01C1/06 , C07D487/04
CPC分类号： A01N43/90 , C07D487/04
摘要： Substituted triazolopyrimidines of the formula I in which the substituents are as defined below: R1 is alkyl, halocycloalkyl, alkenyl, cycloalkyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle comprising one to four heteroatoms from the group consisting of O, N and S, R2 is hydrogen, alkyl or one of the groups mentioned under R1; R1 and/or R2 may carry one to four identical or different groups Ra: Ra is chlorine, bromine, iodine, cyano, nitro, hydroxyl, alkyl, alkylcarbonyl, cycloalkyl, alkoxy, haloalkoxy, alkoxycarbonyl, alkylthio, alkylamino, dialkyl-amino, alkenyl, cycloalkenyl, alkenyloxy, haloalkenyloxy, alkynyl, halo-alkynyl, alkynyloxy, haloalkynyloxy, cycloalkoxy, cycloalkenyloxy, oxyalkylenoxy, naphthyl, a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle comprising one to four heteroatoms from the group consisting of O, N and S, where these aliphatic, alicyclic or aromatic groups for their part may be substituted according to the description; and X is halogen; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
摘要翻译：取代基如下定义的式I的取代三唑并嘧啶：R 1是烷基，卤代环烷基，烯基，环烷基，环烯基，卤代环烯基，炔基，卤代炔基或萘基，或五或六元环，包含一至四个由O，N和S组成的组的杂原子的2-元饱和的，部分不饱和的或芳族的杂环，R 2是氢，烷基或R 1上提到的基团之一， / SUP>; R 1和/或R 2可以携带一至四个相同或不同的基团R a是：R a是氯，溴，碘，氰基，硝基，羟基，烷基，烷基羰基，环烷基，烷氧基，卤代烷氧基，烷氧基羰基，烷硫基，烷基氨基，二烷基氨基，烯基，环烯基，烯氧基，卤代烯氧基，炔基，卤代炔基，炔氧基，卤代炔氧基，环烷氧基，环烯氧基，氧亚烷基氧基，萘基，五至十元饱和的部分不饱和或芳族杂环，其包含一至四个由O，N和S组成的组的杂原子，其中这些脂族，脂环族或芳族基团可以根据描述进行替代; X为卤素; 制备这些化合物的方法，包含它们的组合物及其用于控制植物病原性有害真菌的用途。

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