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. 发明申请

US20080248952A1 Substituted 6-Phenyl-7-Aminotriazolopyrimidines, Method for the Production Thereof, Their Use for Controlling Pathogenic Fungi, and Agents Containing These Compounds 审中-公开
标题翻译：取代的6-苯基-7-氨基三唑并嘧啶，其制备方法，其用于控制致病真菌和含有这些化合物的试剂
公开(公告)号：US20080248952A1
公开(公告)日：2008-10-09
申请号：US11631004
申请日：2005-07-06
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： C07D487/04 , A01N43/90 , A01N25/00
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, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, 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 or a group R1, R1 and R2 together with the nitrogen atom, to which they are attached, may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and which may comprise one to three further heteroatoms from the groups consisting of O, N and S as ring member and/or may be substituted according to the description; L is fluorine, chlorine or methyl; X is cyano, C1-C4-alkyl, C1-C4-alkoxy or C1-C2-haloalkoxy, where X is not methyl if R1 and R2 together are n-pentylene or 3-methyl-n-pentylene and L is fluorine, or R1 and R2 together are 3-methyl-n-pentylene and L is chlorine; processes and intermediates 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：式I的取代三唑并嘧啶：R 1是烷基，卤代烷基，环烷基，卤代环烷基，烯基，卤代烯基，环烯基，卤代环烯基，炔基，包含一至四个由O，N和S组成的组的杂原子的五或六元饱和的部分不饱和或芳族杂环，R 2是氢或基团R 1， R 1，R 2和R 2与它们所连接的氮原子一起也可以形成五元或六元杂环基或杂芳基，它们是通过N连接并且其可以包含一个至三个由O，N和S组成的基团的另外的杂原子作为环成员和/或可以根据描述被取代; L是氟，氯或甲基; X是氰基，C 1 -C 4 - 烷基，C 1 -C 4 - 烷氧基或C 1 -C 4 - 如果R 1和R 2一起都是正 - 亚戊基，其中X不是甲基，其中X不是甲基或3-甲基 - 正戊烯，L是氟，R 1和R 2一起是3-甲基 - 正戊烯，L是氯; 制备这些化合物的方法和中间体，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。

2. 发明申请

US20080227795A1 6(2-Chloro-5-Halophenyl)Triazolopyrimidines, Their Preparation And Their Use For Controlling Harmful Fungi, And Compositions Comprising These Compounds 审中-公开
标题翻译： 6（2-氯-5-卤代苯基）三唑并嘧啶，它们的制备及其用于控制有害真菌及其组合物的用途
公开(公告)号：US20080227795A1
公开(公告)日：2008-09-18
申请号：US10585992
申请日：2005-01-15
申请人： Jordi Tormo i Blasco , Carsten Blettner , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Jordi Tormo i Blasco , Carsten Blettner , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A01N43/90 , C07D487/04 , A01P3/00
CPC分类号： C07D487/04 , A01N43/90
摘要： The invention relates to substituted triazolopyrimidines of formula (I), with the substituents as follows: R1, R2=H, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkinyl, haloalkinyl, phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle, comprising one to four heteroatoms of the group O, N or S, R1 and R2 can, together with the nitrogen atom to which it is attached, form a five- or six-membered heterocycle or heteroaryl, bonded via N and containing one to three further heteroatoms from the group O, N and S as ring members, substituted as per the description, L1=fluorine, chlorine or bromine, L2=H, alkyl or alkoxy and X=halogen, cyano, alkyl, haloalkyl, alkoxy or haloalkoxy. The invention further relates to methods and intermediates for production of said compounds, agents comprising the same and use thereof for controlling fungal pests harmful to plants.
摘要翻译：本发明涉及式（I）的取代三唑并嘧啶，其取代基如下：R 1，R 2 = H，烷基，卤代烷基，环烷基，卤代环烷基，烯基，卤代烯基，环烯基，卤代环烯基，炔基，卤代炔基，苯基，萘基或五元或六元饱和的部分不饱和或芳族杂环，其包含一至四个O，N或S的杂原子， / SUP>和R 2可以与其所连接的氮原子一起形成五元或六元杂环或杂芳基，其通过N键合并含有一至三个其它杂原子基团O，N和S作为环成员，根据描述被取代，L 1 =氟，氯或溴，L 2 = H，烷基或烷氧基，X = 卤素，氰基，烷基，卤代烷基，烷氧基或卤代烷氧基。本发明还涉及用于生产所述化合物的方法和中间体，包含该化合物的试剂和用于控制对植物有害的真菌害虫的用途。

3. 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.

4. 发明申请

US20070275981A1 (Hetero)Cyclycarboxamides for Controlling Pathogenic Fungi 审中-公开
公开(公告)号：US20070275981A1
公开(公告)日：2007-11-29
申请号：US11661922
申请日：2005-09-05
申请人： Markus Gewehr , Thomas Grote , Bernd Muller , Wassilios Grammenos , Anja Schwogler , Joachim Rheinheimer , Carsten Blettner , Peter Schafer , Frank Schieweck , Oliver Wagner , Jan Rether , Siefgried Strathmann , Reinhard Stierl , Maria Scherer
发明人： Markus Gewehr , Thomas Grote , Bernd Muller , Wassilios Grammenos , Anja Schwogler , Joachim Rheinheimer , Carsten Blettner , Peter Schafer , Frank Schieweck , Oliver Wagner , Jan Rether , Siefgried Strathmann , Reinhard Stierl , Maria Scherer
IPC分类号： A01N43/40 , A01N43/54 , A01P3/00 , C07D239/28 , C07D401/04
CPC分类号： A01N43/78 , A01N43/56 , C07D213/82 , C07D231/40 , C07D277/56 , C07D333/38 , C07D401/12 , C07D403/12 , C07D409/12 , C07D417/12
摘要： The invention relates to the use of (hetero)cyclylcarboxamides of general formula (I) and to the agriculturally useful salts thereof for controlling plant pathogenic fungi, the variables in formula (I) having the following designations: A represents phenyl or an at least monosaturated five-membered or six-membered heterocycle with 1, 2 or 3 heteroatoms as ring members selected from N, O, S, S(═O) and S(═O)2, where phenyl and the at least monosaturated five-membered or six-membered heterocycle can be unsubstituted or substituted according to the description; Y represents oxygen or sulphur; R1 represents H, OH, alkyl, cycloalkyl, alkoxy, halogenalkyl, halogencycloalkyl or halogenalkoxy; R2 and R3 represent H, halogen, nitro, CN, alkyl, cycloalkyl, alkenyl, alkinyl, alkoxy, halogenalkyl, halogencycloalkyl, halogenalkenyl, halogenalkinyl or halogenalkoxy; R4 represents halogen, nitro, CN, alkyl, cycloalkyl, alkenyl, alkinyl, alkoxy, halogenalkyl, halogencycloalkyl, halogenalkenyl, halogenalkinyl or halogenalkoxy; R5 represents hydrogen, halogen, nitro, CN, OH, alkyl, cycloalkyl, alkenyl, alkinyl, alkoxy, alkenyloxy, alkinyloxy, alkoxyalkoxy, halogenalkyl, halogencycloalkyl, halogenalkenyl, halogenalkinyl or halogenalkoxy; alklthio, halogenalkylthio, alkylsulfinyl, halogenalkylsulfinyl, alkylsulfonyl, halogenalkylsulfonyl, —(CR6)═NOR7, —C(O)R8, NR9R10, —C(O)NR9R10, —C(S)NR9R10, phenyl or phenylalkyl, the phenyl ring in the last two radicals optionally comprising between 1 and 4 of the radicals cited for R4; R6, R7, R8, R9 and R10 have the designations cited in the description; the two radicals R4 and R5 bound to adjacent carbon atoms can also represent an alkylene chain with 3 to 5 members, wherein 1 or 2 non-adjacent CH2 groups can also be replaced by O or S, and part or all of the hydrogens can be replaced by halogen; Ar represents phenyl, naphtyl or a five-membered or six-membered heteroaromatic radical with 1, 2 or 3 heteroatoms as ring members selected from N, O, and S, that can optionally also carry a fused benzene ring; and n represents 0, 1, 2, 3, or 4. The invention also relates to crop protection agents containing said compounds.

5. 发明申请

US20070249634A1 Triazolopyrimidine Compounds and Use Thereof for Controlling Harmful Fungi 审中-公开
公开(公告)号：US20070249634A1
公开(公告)日：2007-10-25
申请号：US11597409
申请日：2005-06-08
申请人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bern Muller , Matthias Niedenbruck , Joachim Rheinheimer , Petere Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Liliana Rapado , Michael Rack , Barbara Nave , Maria Schere , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Carsten Blettner , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Udo Hunger , Bern Muller , Matthias Niedenbruck , Joachim Rheinheimer , Petere Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Liliana Rapado , Michael Rack , Barbara Nave , Maria Schere , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A01N43/90 , A01P3/00
CPC分类号： A01N43/90
摘要： The invention relates to the use of triazolopyrimidines of the formula I In which: R1, R2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, alkadienyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl, C3-C6-cycloalkynyl, phenyl, naphthyl, or a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which contains one, two, three or four heteroatoms from the group consisting of O, N and S, where R1, R2 may be substituted as defined in the description or R1 and R2 together with the nitrogen atom to which they are attached may form five- to eight-membered heterocyclyl or heteroaryl which is attached via nitrogen and may contain one, two or three further heteroatoms from the group consisting of O, N and S as ring members and/or may be substituted as defined in the description; L independently of one another are halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyloxy, cyano, C(═O)A1, S(═O)mA2, NRcRd or NRc—(C═O)—Rd, where A1, A2, Rc, Rd and m are as defined in the description; L1 is halogen, alkyl or haloalkyl; L2 is nitro, a group —C(S)NR3R4, a group —C(═N—OR5)(NR6R7) or a group —C(═N—NR8R9)(NR10OR11); X is halogen, cyano, alkyl, alkoxy, haloalkyl or haloalkoxy; R3, R4, R5, R6, R7, R8, R9, R10 and R11 are independently of one another selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl and alkynyl, where the 4 last-mentioned radicals may be substituted as defined in the description; or R3 and R4, or R6 and R7, or R8 and R9 or R10 and R11 together with the nitrogen atom to which they are attached form a four, five, or six-membered saturated or partially unsaturated ring which may be substituted as defined in the description; n is 0, 1, 2 or 3; and the agriculturally acceptable salts thereof, novel triazolopyrimidines, crop protection compositions comprising at least one compound of the formula I and at least one solid or liquid carrier, and a method for controlling phytopathogenic harmful fungi.

6. 发明申请

US20070197389A1 Azolopyrimidine compounds and use thereof for combating parasitic fungi 审中-公开
标题翻译：偶氮嘧啶化合物及其用于防治寄生真菌的用途
公开(公告)号：US20070197389A1
公开(公告)日：2007-08-23
申请号：US10589496
申请日：2005-02-24
申请人： Anja Schwogler , Markus Gewehr , Bernd Muller , Thomas Grote , Wassilios Grammenos , Jordi Blasco , Joachim Rheinheimer , Carsten Blettner , Peter Schafer , Frank Schieweck , Oliver Wagner , Reinhard Stierl , Ulrich Schofl , Siegfried Strathmann , Maria Scherer
发明人： Anja Schwogler , Markus Gewehr , Bernd Muller , Thomas Grote , Wassilios Grammenos , Jordi Blasco , Joachim Rheinheimer , Carsten Blettner , Peter Schafer , Frank Schieweck , Oliver Wagner , Reinhard Stierl , Ulrich Schofl , Siegfried Strathmann , Maria Scherer
IPC分类号： A01N43/713 , C07D487/02
CPC分类号： C07D487/04
摘要： The invention relates to azolopyrimidine compounds of general formula (I), wherein A represents N or C—R6; X and Y, independent of one another, represent a chemical compound or oxygen, sulphur or a group N—R7; the variables R1, R2, R3, R4, R5, R6 and R7 have the meanings cited in the claims and the description. The invention also relates to tautomers of compounds of formula (I) and to the agriculturally compatible salts of compounds (I) and of the tautomers thereof. The invention further relates to the use of azolopyrimidine compounds of general formula (I), to the tautomers thereof and to the agriculturally compatible salts thereof which are used to combat phytopathogenic fungi, and to a method for combating phytopathogenic fungi and means for combating fungi, said means containing at least one compound of general formula (I), a tautomer of formula (I) and/or an agriculturally compatible salt thereof or the tautomer thereof and at least one liquid or solid carrier medium.
摘要翻译：本发明涉及通式（I）的偶氮嘧啶化合物，其中A代表N或C-R 6; X和Y彼此独立地表示化合物或氧，硫或基团N-R 7; 变量R 1，R 2，R 3，R 4，R 5，...，SUP >，R 6和R 7具有权利要求书和说明书中引用的含义。本发明还涉及式（I）化合物和化合物（I）的农业相容盐及其互变异构体的互变异构体。本发明还涉及通式（I）的偶氮嘧啶化合物与其互变异构体及其与植物致病真菌的农业相容盐的用途，以及用于防治植物病原性真菌的方法和对抗真菌的方法，所述方法含有至少一种通式（I）的化合物，式（I）的互变异构体和/或其农业上相容的盐或其互变异构体和至少一种液体或固体载体介质。

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

US20070117852A1 (Hetero)cyclyl carboxanilides for controlling harmful fungi 审中-公开
标题翻译：（异构）环状羧酰苯胺，用于控制有害真菌
公开(公告)号：US20070117852A1
公开(公告)日：2007-05-24
申请号：US10582040
申请日：2004-12-22
申请人： Markus Gewehr , Bernd Muller , Thomas Grote , Wassilios Grammenos , Jordi Tormo i Blasco , Anja Schwogler , Joachim Rheinheimer , Carsten Blettner , Peter Schafer , Frank Schieweck , Oliver Wagner , John-Bryan Speakman , Jan Rether , Siegfried Strathmann , Reinhard Stierl
发明人： Markus Gewehr , Bernd Muller , Thomas Grote , Wassilios Grammenos , Jordi Tormo i Blasco , Anja Schwogler , Joachim Rheinheimer , Carsten Blettner , Peter Schafer , Frank Schieweck , Oliver Wagner , John-Bryan Speakman , Jan Rether , Siegfried Strathmann , Reinhard Stierl
IPC分类号： A01N43/56 , A01N43/40 , A01N43/78 , C07D213/24
CPC分类号： C07D213/82 , A01N43/40 , A01N43/56 , A01N43/78 , A01N47/48 , C07C251/38 , C07D207/34 , C07D231/14 , C07D263/34 , C07D277/56 , C07D279/12 , C07D307/30 , C07D307/54 , C07D307/71 , C07D333/38
摘要： The present invention relates to (hetero)cyclylcarboxanilides of the formula I, in which n is 0, 1, 2, 3 or 4; and m is 1, 2 or 3, Y is oxygen or sulfur; A is unsubstituted or substituted phenyl or is an at least monounsaturated, unsubstituted or substituted 5- or 6-membered heterocycle, R1, R2, R3m, R4m, R5 and R6 are as defined in claim 1, and their agriculturally useful salts. Moreover, the present invention relates to the use of the (hetero)cyclylcarboxanilides of the formula I and their agriculturally useful salts as fungicides, and to crop protection compositions comprising these compounds.
摘要翻译：本发明涉及式（I）的（杂）环己基甲酰苯胺，其中n为0,1,2,3或4; m为1,2或3，Y为氧或硫; A是未取代或取代的苯基，或至少是一个不饱和的，未取代的或取代的5元或6元杂环，R 1，R 2，R 3， R 4，R 5，R 5和R 6如权利要求1所定义，及其农业上有用的盐。此外，本发明涉及式I的（杂）环己基甲酰苯胺及其农业上有用的盐作为杀真菌剂，以及包含这些化合物的作物保护组合物的用途。

9. 发明申请

US20070105873A1 2-Substituted pyrimidines 失效
标题翻译： 2-取代的嘧啶
公开(公告)号：US20070105873A1
公开(公告)日：2007-05-10
申请号：US10564013
申请日：2004-07-15
申请人： Anja Schwogler , Markus Gewehr , Bernd Muller , Thomas Grote , Wassilios Grammenos , Jordi Blasco , Andreas Gypser , Joachim Rheinheimer , Carsten Blettner , Peter Schafer , Frank Schieweck , Oliver Wagner , Reinhard Stierl , Ulrich Schofl , Siegfried Strathmann , Maria Scherer
发明人： Anja Schwogler , Markus Gewehr , Bernd Muller , Thomas Grote , Wassilios Grammenos , Jordi Blasco , Andreas Gypser , Joachim Rheinheimer , Carsten Blettner , Peter Schafer , Frank Schieweck , Oliver Wagner , Reinhard Stierl , Ulrich Schofl , Siegfried Strathmann , Maria Scherer
IPC分类号： A01N43/54
CPC分类号： C07D239/42
摘要： The invention relates to 2-substituted pyrimidines of the formula I in which the index n and the substituents R1 to R3 and L are as defined in the description and R4 corresponds to one of the formulae in which Ra, X and Rb are as defined in the description; and also to processes for preparing these compounds, to pesticidal compositions comprising these compounds and to their use as pesticides.
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 3和L如说明书中所定义， SUP> 4 对应于其中R a，S，X和R b的定义之一如说明书中所定义; 以及制备这些化合物的方法，包括这些化合物的农药组合物及其作为农药的用途。

10. 发明申请

US20060229328A1 2-Substituted pyrimidines 失效
公开(公告)号：US20060229328A1
公开(公告)日：2006-10-12
申请号：US10549936
申请日：2004-03-30
申请人： Jordi i Blasco , Carsten Blettner , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Andreas Gypser , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
发明人： Jordi i Blasco , Carsten Blettner , Bernd Muller , Markus Gewehr , Wassilios Grammenos , Thomas Grote , Andreas Gypser , Joachim Rheinheimer , Peter Schafer , Frank Schieweck , Anja Schwogler , Oliver Wagner , Maria Scherer , Siegfried Strathmann , Ulrich Schofl , Reinhard Stierl
IPC分类号： A01N43/54 , C07D239/02
CPC分类号： A01N43/54 , C07D239/28 , C07D239/30
摘要： 2-Substituted pyrimidines of the formula I in which the index n and the substituents L, Ra, Rb, Rc, Rz, Ru, Rv, A′, A″ and A′″ are as defined in the description and: R1 is C3-C10-alkyl, C3-C10-alkenyl, C3-C10-alkynyl, C3-C12-cycloalkyl, C3-C10-cycloalkenyl or a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which is attached via carbon and contains one to four heteroatoms from the group consisting of O, N and S, R2 is halogen, cyano, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-alkoxy, C3-C4-alkenyloxy or C3-C4-alkynyloxy, where the alkyl, alkenyl and alkynyl radicals of R2 may be substituted by halogen, cyano, nitro, C1-C2-alkoxy or C1-C4-alkoxycarbonyl, and R3 is cyano, CO2Ra, C(═O)NRzRb, C(═O)—N—ORb, C(═S)—NRaRb, C(═NORa)NRzRb, C(═NRa)NRzRb, C(═O)NRa—NRzRb, C(═N—NRzRc)NRaRb, C(═O)Ra, C(═NORb)Ra, C(═N—NRzRb)Ra, CRaRb—ORz, CRaRb—NRzRc, ON(═CRaRb), O—C(═O)Ra, NRaRb′, NRa(C(═O)Rb), NRa(C(═O)ORb), NRa(C(═O)—NRzRb), NRa(C(═NRc)Rb), NRa(N═CRcRb), NRa—NRzRb, NRz—ORa, NRa(C(═NRc)—NRzRb), NRa(C(═NORc)Rb), processes for preparing these compounds, compositions comprising these compounds and their pesticidal use are described.

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