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1. 发明授权

US09288996B2 Fungicidal compositions comprising a phosphate solubilizing microorganism and a fungicidally active compound 有权
标题翻译：包含磷酸盐增溶微生物和杀真菌活性化合物的杀真菌组合物
公开(公告)号：US09288996B2
公开(公告)日：2016-03-22
申请号：US13634890
申请日：2011-03-14
申请人： Thorsten Jabs , Paul Cavell , Sarah Dunker , Alexander Wissemeier , Egon Haden , Tom Wetjen
发明人： Thorsten Jabs , Paul Cavell , Sarah Dunker , Alexander Wissemeier , Egon Haden , Tom Wetjen
IPC分类号： A01N25/26 , A01N63/04
CPC分类号： A01N63/04 , A01N2300/00
摘要： The present invention relates to a composition, comprising a microorganism of species Penicillium bilaji and at least one compound (II) in a synergistically effective amount.
摘要翻译：本发明涉及一种组合物，其包含物质青霉属微生物和至少一种协同有效量的化合物（II）。

2. 发明申请

US20130017949A1 Fungicidal Compositions Comprising a Phosphate Solubilizing Microorganism and a Fungicidally Active Compound 有权
标题翻译：包含磷酸盐溶解微生物和杀真菌活性化合物的杀真菌组合物
公开(公告)号：US20130017949A1
公开(公告)日：2013-01-17
申请号：US13634890
申请日：2011-03-14
申请人： Thorsten Jabs , Paul Cavell , Sarah Dunker , Alexander Wissemeier , Egon Haden , Tom Wetjen
发明人： Thorsten Jabs , Paul Cavell , Sarah Dunker , Alexander Wissemeier , Egon Haden , Tom Wetjen
IPC分类号： A01N63/04 , A01C1/06 , A01P3/00
CPC分类号： A01N63/04 , A01N2300/00
摘要： The present invention relates to a composition, comprising a microorganism as defined in the description and at least one compound (II) selected from groups A) to F) as defined in the description in a synergistically effective amount.
摘要翻译：本发明涉及一种组合物，其包含如说明书中所定义的微生物和至少一种选自组合A）至F）的化合物（II），如协同有效量的描述中所定义。

3. 发明申请

US20130040813A1 Fungicidal mixtures II comprising quinazolines 审中-公开
标题翻译：杀真菌混合物II包含喹唑啉
公开(公告)号：US20130040813A1
公开(公告)日：2013-02-14
申请号：US13640592
申请日：2011-04-12
申请人： Bernd Mueller , Thorsten Jabs , Jan Klaas Lohmann , Wassilios Grammenos , Marianna Vrettou-Schultes , Egon Haden
发明人： Bernd Mueller , Thorsten Jabs , Jan Klaas Lohmann , Wassilios Grammenos , Marianna Vrettou-Schultes , Egon Haden
IPC分类号： A01N43/54 , A01C1/06 , A01P3/00
CPC分类号： A01N43/54 , A01N37/34 , A01N37/50 , A01N43/42 , A01N43/56 , A01N43/653 , A01N47/24 , A01N2300/00
摘要： The present invention relates to fungicidal mixtures, comprising at least one quinazoline compound I and one compound II as defined in the description, and to compositions comprising these mixtures.
摘要翻译：本发明涉及杀真菌混合物，其包含至少一种如说明书中定义的喹唑啉化合物I和一种化合物II以及包含这些混合物的组合物。

4. 发明申请

US20130035229A1 FUNGICIDAL MIXTURES I COMPRISING QUINAZOLINES 审中-公开
标题翻译：真菌混合物包括喹诺酮类
公开(公告)号：US20130035229A1
公开(公告)日：2013-02-07
申请号：US13640361
申请日：2011-04-12
申请人： Bernd Müller , Thorsten Jabs , Jan Klaas Lohmann , Wassilios Grammenos , Marianna Vrettou-Schultes , Egon Haden
发明人： Bernd Müller , Thorsten Jabs , Jan Klaas Lohmann , Wassilios Grammenos , Marianna Vrettou-Schultes , Egon Haden
IPC分类号： A01N43/54 , A01P3/00 , A01N63/02 , A01N63/04 , A01C1/06 , A01N43/56
CPC分类号： A01N43/54 , A01N43/36 , A01N43/56 , A01N43/653 , A01N63/00 , A01N2300/00
摘要： The present invention relates to fungicidal mixtures, comprising at least one quinazo-line compound I and one compound II as defined in the description, and to compositions comprising these mixtures.
摘要翻译：本发明涉及杀真菌混合物，其包含至少一种如说明书中所定义的喹唑啉化合物I和一种化合物II，以及包含这些混合物的组合物。

5. 发明授权

US08716487B2 Process for preparing 4-hydroxypyridines 有权
标题翻译：制备4-羟基吡啶的方法
公开(公告)号：US08716487B2
公开(公告)日：2014-05-06
申请号：US13805567
申请日：2011-06-20
申请人： Volker Maywald , Frederik Menges , Uwe Josef Vogelbacher , Michael Rack , Michael Keil , Wassilios Grammenos , Marianna Vrettou-Schultes , Jan Klaas Lohmann , Bernd Mueller , Thorsten Jabs
发明人： Volker Maywald , Frederik Menges , Uwe Josef Vogelbacher , Michael Rack , Michael Keil , Wassilios Grammenos , Marianna Vrettou-Schultes , Jan Klaas Lohmann , Bernd Mueller , Thorsten Jabs
IPC分类号： C07D213/08 , C07D213/68
CPC分类号： C07D213/68 , C07D213/08 , C07D213/61
摘要： The present invention relates to a process for preparing 4-hydroxypyridines of formula I wherein R1, R2, R3 and R4 have the meanings defined in the description.
摘要翻译：本发明涉及制备式I的4-羟基吡啶的方法，其中R1，R2，R3和R4具有说明书中定义的含义。

6. 发明申请

US20080146593A1 Substituted 5-Phenyl Pyrimidines I In Therapy 审中-公开
公开(公告)号：US20080146593A1
公开(公告)日：2008-06-19
申请号：US11815042
申请日：2006-01-30
申请人： Joachim Rheinheimer , Thomas Grote , Bernd Muller , Barbara Nave , Frank Schieweck , Anja Schwogler , Thorsten Jabs , Carsten Blettner
发明人： Joachim Rheinheimer , Thomas Grote , Bernd Muller , Barbara Nave , Frank Schieweck , Anja Schwogler , Thorsten Jabs , Carsten Blettner
IPC分类号： A61K31/505 , A61K31/513 , A61P35/00
CPC分类号： C07D239/48 , C07D239/42 , C07D401/04 , C07D403/04 , C07D417/04
摘要： The present invention relates to substituted 5-phenyl pyrimidines I, which carry a radical X in the 4-position of the pyrimidine ring, a radical Y in the 6-position of the pyrimidine ring, the radical X denoting a group of the formula NR1R2, OR1a or SR1a, in which R1, R2, independently of each other, denote hydrogen, C1-C10-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C10-haloalkyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, phenyl, or 5- or 6-membered heteroaryl or 5- or 6-membered heterocyclyl, containing 1, 2, 3 or 4 nitrogen atoms or 1, 2 or 3 nitrogen atoms and one sulfur or oxygen atom as ring members, which radicals may be unsubstituted or may carry 1, 2, 3 or 4 radicals Ra1; or the radical NR1R2 may also form a 5- or 6-membered optionally substituted heterocyclic ring, containing 1, 2, 3 or 4 nitrogen atoms or 1, 2 or 3 nitrogen atoms and one sulfur or oxygen atom as ring members, which are non-adjacent to the nitrogen of NR1R2, in which two adjacent C atoms or one N atom and one adjacent C atom can be linked by a C1-C4-alkylene chain and wherein the heterocyclic ring may be unsubstituted or may carry 1, 2, 3 or 4 radicals Ra1 as defined in claim 1, R1a has one of the meanings given for R1 except for hydrogen; the radical Y being selected from the group consisting of halogen, cyano, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C3-C6-cycloalkyl, C1-C4-alkoxy, C3-C4-alkenyloxy, C3-C4-alkynyloxy, C1-C6-alkylthio, di-(C1-C6-alkyl)amino or C1-C6-alkylamino, where the alkyl, alkenyl and alkynyl radicals of Y may be substituted by halogen, cyano, nitro, C1-C2-alkoxy or C1-C4-alkoxycarbonyl; and wherein the pyrimidine radical may also carry a radical different from hydrogen in the 2-position and wherein the phenyl ring in the 5-position of the pyrimidine ring may be unsubstituted or carry 1, 2, 3, 4 or 5 radicals L which are different from hydrogen, and the pharmaceutically acceptable salts substituted 5-phenyl pyrimidines for use in therapy, in particular in therapy or treatment of cancerous diseases.

7. 发明申请

US20070185099A1 Triazolopyrimidine compounds and their use for controlling pathogenic fungi 审中-公开
标题翻译：三唑并嘧啶化合物及其用于控制致病真菌的用途
公开(公告)号：US20070185099A1
公开(公告)日：2007-08-09
申请号：US11628852
申请日：2005-06-24
申请人： Carsten Blettner , Frank Schieweck , Jordi i Blasco , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Joachim Rheinheimer , Peter Schafer , Anja Schwogler , Oliver Wagner , John-Bryan Speakman , Thorsten Jabs , Siegfried Strathmann , Ulrich Schofl , Maria Scherer , Reinhard Stierl
发明人： Carsten Blettner , Frank Schieweck , Jordi i Blasco , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Joachim Rheinheimer , Peter Schafer , Anja Schwogler , Oliver Wagner , John-Bryan Speakman , Thorsten Jabs , Siegfried Strathmann , Ulrich Schofl , Maria Scherer , Reinhard Stierl
IPC分类号： A01N43/90 , C07D487/04
CPC分类号： A01N43/90 , C07D487/04
摘要： The present invention relates to novel triazolopyrimidine compounds of the formula I in which: X is halogen, cyano, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1-C2-haloalkoxy; W is oxygen or sulfur; Y is O—R4 or a group NR5R6; A is a chemical bond or a group CR7R8; and the variables L, R1 to R7 are as defined in claim 1. The present invention furthermore provides the use of the triazolopyrimidine compounds of the formula I, their tautomers and their agriculturally acceptable salts for controlling phytopathogenic fungi (=harmful fungi) and a method for controlling phytopathogenic harmful fungi, which method comprises treating the fungi or the materials, plants, the soil or seed to be protected against fungal attack with an effective amount of a compound of the formula I, a tautomer of I and/or an agriculturally acceptable salt of I or a tautomer thereof.
摘要翻译：本发明涉及新的式I的三唑并嘧啶化合物，其中：X为卤素，氰基，C 1 -C 4 - 烷基，C 1〜 C 1 -C 4 - 低级烷基，C 1 -C 4 - 烷氧基或C 1 -C 3 > 2 - 卤代烷氧基; W是氧或硫; Y是O-R 4或NR 5或R 6基团; A是化学键或基团CR 7 R 8; 变量L，R 1至R 7如权利要求1中所定义。本发明还提供式I的三唑并嘧啶化合物，其互变异构体和其用于控制植物病原真菌（=有害真菌）的农业上可接受的盐和控制植物病原性有害真菌的方法，所述方法包括用有效量的有效量处理待保护的真菌或植物，土壤或种子免受真菌侵袭式I的化合物，I的互变异构体和/或I的农业上可接受的盐或其互变异构体。

8. 发明申请

US20130096312A1 Process for Preparing 4-hydroxypyridines 有权
标题翻译： 4-羟基吡啶的制备方法
公开(公告)号：US20130096312A1
公开(公告)日：2013-04-18
申请号：US13805567
申请日：2011-06-20
申请人： Volker Maywald , Frederik Menges , Uwe Josef Vogelbacher , Michael Rack , Michael Keil , Wassilios Grammenos , Marianna Vrettou-Schultes , Jan Klaas Lohmann , Bernd Mueller , Thorsten Jabs
发明人： Volker Maywald , Frederik Menges , Uwe Josef Vogelbacher , Michael Rack , Michael Keil , Wassilios Grammenos , Marianna Vrettou-Schultes , Jan Klaas Lohmann , Bernd Mueller , Thorsten Jabs
IPC分类号： C07D213/68 , C07D213/61
CPC分类号： C07D213/68 , C07D213/08 , C07D213/61
摘要： The present invention relates to a process for preparing 4-hydroxypyridines of formula I wherein R1, R2, R3 and R4 have the meanings defined in the description.
摘要翻译：本发明涉及制备式I的4-羟基吡啶的方法，其中R1，R2，R3和R4具有说明书中定义的含义。

9. 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。

10. 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.

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