专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

41. 发明申请

US20090029855A1 Quinoline Derivatives and Their Use as Pesticides 审中-公开
标题翻译：喹啉衍生物及其作为农药的用途
公开(公告)号：US20090029855A1
公开(公告)日：2009-01-29
申请号：US12282608
申请日：2007-03-12
申请人： Michael Puhl , Wassilios Grammenos , Joachim Rheinheimer , Jan Klaas Lohmann , Michael Rack , Liliana Parra Rapado , Christopher Koradin , Jurgen Langewald , Deborah L. Culbertson , Douglas D. Anspaugh , Hassan Oloumi-Sadeghi , Henry Van Tuyl Cotter , David G. Kuhn
发明人： Michael Puhl , Wassilios Grammenos , Joachim Rheinheimer , Jan Klaas Lohmann , Michael Rack , Liliana Parra Rapado , Christopher Koradin , Jurgen Langewald , Deborah L. Culbertson , Douglas D. Anspaugh , Hassan Oloumi-Sadeghi , Henry Van Tuyl Cotter , David G. Kuhn
IPC分类号： A01N25/26 , C07D215/14 , A01N43/42 , A01N59/26 , A01P5/00 , A01P7/04
CPC分类号： C07D215/12 , C07D215/60
摘要： This invention relates to quinoline derivatives of formula I wherein R1, R2, R3 are each independently halogen, hydroxy, cyano, amino, nitro, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, C1-C6-alkoxy, C2-C6-alkenyloxy, C2-C6-alkynyloxy, C1-C4-alkoxy-C1-C4-alkoxy, C3-C7-cycloalkyl-C1-C4-alkoxy, C(OH)(CF3)2, C1-C6-haloalkyl, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, C(Ra)═O, C(Ra)═NORb, C(═O)ORx, or C(═O)NRxRy; Ra is hydrogen or C1-C4-alkyl; Rb is hydrogen, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-haloalkyl, or C2-C4-haloalkenyl; Rx, Ry are each independently hydrogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-thioalkyl-C1-C4-alkyl, C1-C4-alkyl-S(═O)C1-C4-alkyl, C1-C4-alkyl-S(═O)2C1-C4-alkyl, C3-C6-cyloalkyl, C1-C4-alkyl-C3-C6-cycloalkyl, C3-C6-alkenyl, C3-C6-alkinyl; R4, R5, R6, R7 are each independently hydrogen, halogen, cyano, amino, nitro, hydroxy, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-haloalkyl, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, or C(═O)ORc; Rc is hydrogen, C1-C6-alkyl, C2-C6-alkenyl, or C2-C6-alkinyl; m and n are each independently 1, 2, 3, 4, or 5; p is 0, 1, 2, 3, 4, or 5; and the N-oxides, enantiomers, diastereomers and salts thereof, processes and intermediates for the preparation of compounds I, use of compounds I for combating insects, acarids, or nematodes and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites using compounds I.
摘要翻译：本发明涉及式I的喹啉衍生物，其中R 1，R 2，R 3各自独立地为卤素，羟基，氰基，氨基，硝基，C 1 -C 6烷基，C 2 -C 6 - 烯基，C 2 -C 6炔基，C 3 -C 7 - 环烷基，C 3 -C 7 - 环烷基-C 1 -C 4 - 烷基，C 1 -C 6 - 烷氧基，C 2 -C 6 - 烯氧基，C 2 -C 6 - 炔氧基，C 1 -C 4烷氧基-C 1 -C 4烷氧基，C 3 -C 7 - 环烷基 - C 1 -C 6烷氧基，C（OH）（CF 3）2，C 1 -C 6卤代烷基，C 1 -C 6卤代烷氧基，C 1 -C 6烷硫基，C 1 -C 6卤代烷硫基，C 1 -C 6烷基亚磺酰基， C 1 -C 6烷基磺酰基，C 1 -C 6卤代烷基磺酰基，C（R a）-O，C（R a）-NOR b，C（-O）OR x或C（-O）NR x R y; R a是氢或C 1 -C 4 - 烷基; R b是氢，C 1 -C 4 - 烷基，C 2 -C 4 - 烯基，C 2 -C 4 - 炔基，C 1 -C 4卤代烷基或C 2 -C 4 - 卤代烯基; R x，R y各自独立地为氢，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基-C 1 -C 4烷基，C 1 -C 4 - 硫代烷基-C 1 -C 4烷基，C 1 -C 4烷基 - S（-O）C 1 -C 4 - 烷基，C 1 -C 4烷基-S（-O）2 C 1 -C 4烷基，C 3 -C 6 - 环烷基，C 1 -C 4烷基-C 3 -C 6环烷基，C 3 -C 6 - 烯基，C 3 -C 6 - 炔基; R4，R5，R6，R7各自独立地为氢，卤素，氰基，氨基，硝基，羟基，C1-C6-烷基，C1-C6-烷氧基，C1-C6-卤代烷基，C1-C6-卤代烷氧基，C1-C6- C 1 -C 6烷基亚磺酰基，C 1 -C 6烷基磺酰基，C 1 -C 6卤代烷基磺酰基或C（-O）OR c; R c是氢，C 1 -C 6 - 烷基，C 2 -C 6 - 烯基或C 2 -C 6 - 炔基; m和n各自独立地为1,2,3,4或5; p是0，1，2，3，4或5; 及其N-氧化物，对映异构体，非对映异构体及其盐，制备化合物I的方法和中间体，化合物I用于防治昆虫，螨虫或线虫的用途，以及用于治疗，控制，预防或保护动物免受感染或使用化合物I的寄生虫感染

42. 发明申请

US20080227636A1 Isothiazolopyridin-3-Ylenamines for Combating Animal Pests 审中-公开
标题翻译：异噻唑啉-3-烯胺用于防治动物害虫
公开(公告)号：US20080227636A1
公开(公告)日：2008-09-18
申请号：US12090599
申请日：2006-10-12
申请人： Florian Kaiser , Wolfgang von Deyn , Matthias Pohlman , Henricus Maria Martinus Bastiaans , Douglas D. Anspaugh , Deborah L. Culbertson , Henry Van Tuyl Cotter
发明人： Florian Kaiser , Wolfgang von Deyn , Matthias Pohlman , Henricus Maria Martinus Bastiaans , Douglas D. Anspaugh , Deborah L. Culbertson , Henry Van Tuyl Cotter
IPC分类号： C07D513/04 , A01N43/90 , A01C1/06
CPC分类号： A01N43/90 , C07D513/04
摘要： The present invention relates to Isothiazolopyridin-3-ylenamine compounds of the general formula I and to the agriculturally useful salts thereof and to compositions comprising such compounds. The invention also relates to the use of the Isothiazolopyridin-3-ylenamine compounds, of their salts or of compositions comprising them for combating animal pests. A Isothiazolopyridin-3-ylenamine compound of the present invention is represented by the following formula I:
摘要翻译：本发明涉及通式I的异噻唑并吡啶-3-基胺化合物及其农业上有用的盐以及包含这些化合物的组合物。本发明还涉及异噻唑啉-3-基胺化合物，其盐或其组合物用于对抗动物害虫的用途。本发明的异噻唑啉-3-基胺化合物由下式I表示：

43. 发明申请

US20080214394A1 N-(4-Pyridyl)Methylsulfonamides For Combating Arthropodal Pests 审中-公开
公开(公告)号：US20080214394A1
公开(公告)日：2008-09-04
申请号：US11908744
申请日：2006-03-15
申请人： Michael Puhl , Christopher Koradin , Joachim Rheinheimer , Wassilios Grammenos , Jan Klaas Lohmann , Ernst Baumann , Wolfgang von Deyn , Jurgen Langewald , Norbert Gotz , Douglas D. Anspaugh , Deborah L. Culbertson , Henry Van Tuyl Cotter , Hassan Olumi-Sadeghi
发明人： Michael Puhl , Christopher Koradin , Joachim Rheinheimer , Wassilios Grammenos , Jan Klaas Lohmann , Ernst Baumann , Wolfgang von Deyn , Jurgen Langewald , Norbert Gotz , Douglas D. Anspaugh , Deborah L. Culbertson , Henry Van Tuyl Cotter , Hassan Olumi-Sadeghi
IPC分类号： A01N43/40 , C07D215/36 , C07D401/12 , A61K31/44
CPC分类号： C07D213/42 , A01N43/40 , A01N43/42 , C07D215/12 , C07D409/12
摘要： N-(4-Pyridyl)methylsulfonamides for combating arthropodal pests The present invention relates to the use of N-(4-pyridyl)methylsulfonamides of the formula for combating arthropodal pests (harmful arthropodes) and for protecting materials against infestation and/or destruction by said pests: (I) where the substituents are as follows: R1 is hydrogen, C1-C4-alkyl, C1-C4-alkoxy, C2-C4-alkenyl, C2-C4-alkynyl or benzyl; R2, R3, R4, R5 independently of one another are hydrogen, halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkoxy or C1-C4-haloalkyl; R2 and R3 or R4 and R5 together with the carbon atoms to which they are attached may also form a condensed 5- or 6-membered hydro-carbon ring, it being possible for the hydrocarbon ring to carry one or two groups R2′, R3′, R2′, R3′ independently of one another are halogen, C1-C4-alkyl, C1-C4-alkoxy, halomethoxy or halomethyl; X is a cyclic radical selected from phenyl, naphthyl and five- or six-membered saturated, partially unsaturated or aromatic heterocycles, the heterocycle being attached to the sulfur atom via a carbon atom and containing 1, 2 or 4 heteroatoms selected from the group consisting of O, N and S, where the cyclic radical X may carry 1, 2, 3 or 4 substituents Ra.

44. 发明授权

US06699874B2 Fungicidal mixtures 失效
标题翻译：杀菌混合物
公开(公告)号：US06699874B2
公开(公告)日：2004-03-02
申请号：US10314594
申请日：2002-12-10
申请人： Henry Van Tuyl Cotter , Leslie May , Gunter Reichert , Ewald Sieverding
发明人： Henry Van Tuyl Cotter , Leslie May , Gunter Reichert , Ewald Sieverding
IPC分类号： A01N4354
CPC分类号： A01N43/90 , A01N2300/00
摘要： Fungicidal compositions comprising an acceptable carrier and/or surface active agent and synergistically effective amounts of (a) at least one azolopyrimidine of formula I in which R1, R2, L1, L2 and L3 have the meaning given in claim 1; and (b) at least one fungicidal active ingredient selected from benomyl, carboxin, captan, chlorothalonil, copper oxychloride, cyprodinil, dimethomorph, dithianon, dodine, famoxadone, fenhexamid, fenpiclonil, fenpropimorph, fluazinam, mancozeb, metalaxyl, pyrimethanil, quinoxifen, sulfur, triforine, vinclozolin, a fungicidal triazole derivative, and a synthetic strobilurine derivative. The invention also provides a method of controlling the growth of phytopathogenic fungi at a locus by applying synergistically effective amounts of at least one azolopyrimidine of formula I and at least one fungicidal active ingredient (b) to the locus.
摘要翻译：包含可接受的载体和/或表面活性剂和协同有效量的（a）至少一种R 1，R 2，L 1，L 2和L 3的式Iin的偶氮嘧啶的杀真菌组合物 >具有权利要求1中给出的含义; 和（b）至少一种杀真菌活性成分，其选自苯菌灵，呋喃丹，克拉曼，百菌清，氯氧化铜，西酞替尼，烯酰吗啉，二噻吩，十二烷，恶唑酮，芬己酰，芬替尼，芬卡芬，氟啶胺，代森锰锌，甲霜灵，嘧霉胺，喹喔啉，，triperine，长春菌素，杀真菌三唑衍生物和合成次溴酸衍生物。本发明还提供了一种通过将协同有效量的至少一种式I的偶氮嘧啶和至少一种杀真菌活性成分（b）施用于该基因座来控制植物病原真菌在一个场所生长的方法。

45. 发明授权

US06498194B2 Fungicidal mixtures 有权
标题翻译：杀菌混合物
公开(公告)号：US06498194B2
公开(公告)日：2002-12-24
申请号：US10046190
申请日：2002-01-16
申请人： Henry Van Tuyl Cotter , Gunther Reichert , Ewald Sieverding , Petrus Martinus Franciscus Emanuel Jegerings
发明人： Henry Van Tuyl Cotter , Gunther Reichert , Ewald Sieverding , Petrus Martinus Franciscus Emanuel Jegerings
IPC分类号： A01N3500
CPC分类号： A01N35/04 , A01N59/20 , A01N59/02 , A01N55/00 , A01N47/44 , A01N47/38 , A01N47/14 , A01N47/04 , A01N43/90 , A01N43/84 , A01N43/82 , A01N43/76 , A01N43/653 , A01N43/60 , A01N43/56 , A01N43/54 , A01N43/40 , A01N43/42 , A01N43/36 , A01N43/32 , A01N43/30 , A01N37/50 , A01N37/46 , A01N37/38 , A01N37/34 , A01N37/06 , A01N2300/00
摘要： The invention relates to a novel fungicidal composition comprising a fungicidally acceptable carrier and/or surface active agent together with, and synergistically effective amounts of (a) at least one benzophenone of formula I wherein R1, R2, R3, R4, R5, R6, R7, m and n have the meaning given; at least one fungicidal active ingredient selected from the following groups (A), (B), (C), (D) and (E): (A) an ergosterol biosynthesis inhibitor; (B) a strobilurine derivative, (C) a melanin biosynthesis inhibitor; (D) a compound selected from the group consisting of acibenzolar, benomyl, captan, carboxin, chlorothalonil, copper, cyprodinil, dinocap, dithianon, dimethomorph, dodine, ethirimol, famoxadone, fenpiclonil, fluazinam, mancozeb, metalaxyl, pyrifenox, sulfur, vinclozolin and (E) an azolopyrimidine of formula II in which R8, R9, R10, R11, A, L and p have the meaning given; and to a method of controlling the growth of phytopathogenic fungi at a locus which comprises applying synergistically effective amounts of (a) at least one benzophenones of formula I and (b) at least one fungicidal active ingredient selected from the groups (A), (B), (C), (D) and (E) to the locus.
摘要翻译：本发明涉及一种新颖的杀真菌组合物，其包含杀真菌剂可接受的载体和/或表面活性剂以及协同有效量的（a）至少一种式I的二苯甲酮，其中R 1，R 2，R 3，R 4，R 5，R 6， R7，m和n具有给定的含义;至少一种选自以下组（A），（B），（C），（D）和（E）:( A）麦芽甾醇生物合成抑制剂的杀真菌活性成分; B）嗜苯西林嘌呤衍生物，（C）黑色素生物合成抑制剂;（D）选自由以下组成的组的化合物：苯偶姻，苯菌灵，克拉曼，羧酸，百菌清，铜，嘧菌胺，二氮烯，二噻吩，烯酰吗啉，，fenpiclonil，氟啶胺，代森锰锌，甲霜灵，pyrifenox，硫，连环素和（E）式II的偶氮嘧啶，其中R8，R9，R10，R11，A，L和p具有给定的含义; 包括应用协同效应的植物病原真菌的生长（a）至少一种式I的二苯甲酮和（b）至少一种选自（A），（B），（C），（D）和（E）的杀真菌活性成分。

46. 发明授权

US06346535B1 Fungicidal mixtures 有权
公开(公告)号：US06346535B1
公开(公告)日：2002-02-12
申请号：US09240412
申请日：1999-01-29
申请人： Henry Van Tuyl Cotter , Gunther Reichert , Ewald Sieverding , Petrus Martinus Franciscus Emanuel Jegerings
发明人： Henry Van Tuyl Cotter , Gunther Reichert , Ewald Sieverding , Petrus Martinus Franciscus Emanuel Jegerings
IPC分类号： A01N4354
CPC分类号： A01N35/04 , A01N59/20 , A01N59/02 , A01N55/00 , A01N47/44 , A01N47/38 , A01N47/14 , A01N47/04 , A01N43/90 , A01N43/84 , A01N43/82 , A01N43/76 , A01N43/653 , A01N43/60 , A01N43/56 , A01N43/54 , A01N43/40 , A01N43/42 , A01N43/36 , A01N43/32 , A01N43/30 , A01N37/50 , A01N37/46 , A01N37/38 , A01N37/34 , A01N37/06 , A01N2300/00
摘要： The invention relates to a novel fungicidal composition comprising synergistically effective amounts of at least one benzophenone of formula I wherein R1 represents a halogen atom, an optionally substituted alkyl, alkanoyloxy or alkoxy group; or a hydroxy group, R2 represents a halogen atom or an optionally substituted alkyl group, R3 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group or a nitro group; m is 0 or an integer of 1 to 3; R4 represents a halogen atom, a cyano, carboxy, hydroxy or nitro group or an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulphinyl, alkylsulphonyl or amino group; R5 represents an optionally substituted alkyl group; R6 represents a halogen atom or a nitro group, an optionally substituted alkyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy, aryloxy group; R7 independently represents a halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkoxy group; n is 0 or 1; and at least one fungicidally active ingredient selected from the groups consisting of (A), (B), (C), (D) and (E) wherein: (A) is an ergosterol biosynthesis inhibitor; (B) is a strobilurine derivative, (C) is a melanin biosynthesis inhibitor; (D) is a compound selected from the group consisting of acibenzolar, benomyl, captan, carboxin, chlorothalonil, copper, cyprodinil, dinocap, dithianon, dimethomorph, dodine, ethirimol, famoxadone, fenpiclonil, fluazinam, mancozeb, metalaxyl, pyrifenox, sulfur, vinclozolin and (E) is an azolopyrimidine of formula II iwherein R8 and R9 each independently represent hydrogen or an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl, aryl, heteroaryl, cycloalkyl, bicycloalkyl or heterocyclyl group, or R8 and R9 together with the interjacent nitrogen atom represent an optionally substituted heterocyclic ring, R10 represents hydrogen or an alkyl or aryl group, R11 represents a hydrogen or halogen atom or an alkyl or alkoxy group, L independently represents a halogen atom or an optionally substituted alkyl or alkoxy group, p is 0 or an integer from 1 to 5; and A represents N or CR2, wherein R12 has the meaning given for R10; together with a fungicidally acceptable carrier and/or surface active agent, and to a method of controlling the growth of phytopathogenic fungi which comprises applying synergistically effective amounts of the composition to the locus.

47. 发明授权

US6127570A Fungicidal substituted 2-hydroxybenzophenones 失效
标题翻译：杀真菌剂取代的2-羟基二苯甲酮
公开(公告)号：US6127570A
公开(公告)日：2000-10-03
申请号：US329712
申请日：1999-06-10
申请人： Juergen Curtze , Gerd Morschhaeuser , Henry Van Tuyl Cotter
发明人： Juergen Curtze , Gerd Morschhaeuser , Henry Van Tuyl Cotter
IPC分类号： C07C45/67 , C07C49/84 , C07C67/307 , C07C69/017 , C07L69/00
CPC分类号： C07C69/21 , C07C45/673 , C07C49/84 , C07C67/08 , C07C67/293 , C07C67/307
摘要： Substituted 2-hydroxybenzophenone compounds are disclosed, having the formula: ##STR1## The compounds are useful as fungicides having high systemicities.
摘要翻译：公开了具有下式的取代的2-羟基二苯甲酮化合物：该化合物可用作具有高系统性的杀真菌剂。

48. 发明授权

US6090806A Fungicidal mixtures 有权
标题翻译：杀菌混合物
公开(公告)号：US6090806A
公开(公告)日：2000-07-18
申请号：US143806
申请日：1998-08-31
申请人： Henry Van Tuyl Cotter
发明人： Henry Van Tuyl Cotter
IPC分类号： A01N43/76 , A01N31/535
CPC分类号： A01N43/76
摘要： The invention relates to fungicidal compositions comprising synergistically effective amounts ofat least one acrylic acid morpholide of formula I ##STR1## in which R.sup.1 and R.sup.2 have the meaning given in claim 1 and at least one fungicidal oxazolidinone of formula II ##STR2## in which R.sup.3.sub.1 R.sup.4 and Ar have the meaning given in claim 1, and to a method of controlling the growth of phythopathogenic fungi and/or the plant disease caused by them at a locus which comprises applying synergistically effective amounts of at least one acrylic acid morpholide of formula I (a) and at least one fungicidal compound of formula II (b) to the locus, together with a fungicidally acceptable carrier and/or surface active agent.
摘要翻译：本发明涉及杀真菌组合物，其包含协同有效量的式I的至少一种丙烯酸吗啉，其中R 1和R 2具有权利要求1中给出的含义，和至少一种式II的杀真菌恶唑烷酮，其中R 31 R 4和Ar具有权利要求1的方法，以及一种控制由它们引起的植物病原真菌和/或植物疾病生长的方法，所述方法包括将协同有效量的至少一种式I（a）的丙烯酸吗啉代和至少一种杀真菌剂式II（b）的化合物与杀真菌剂可接受的载体和/或表面活性剂。

49. 发明授权

US6001883A Fungicidal 2-methoxybenzophenones 失效
公开(公告)号：US6001883A
公开(公告)日：1999-12-14
申请号：US103887
申请日：1998-06-24
申请人： Juergen Curtze , Gerd Morschhaeuser , Henry Van Tuyl Cotter
发明人： Juergen Curtze , Gerd Morschhaeuser , Henry Van Tuyl Cotter
IPC分类号： A01N35/04 , C07C45/46 , C07C45/67 , C07C45/68 , C07C45/70 , C07C45/71 , C07C49/84 , C07C65/21 , C07C65/24 , C07C205/45 , A01N31/16
CPC分类号： C07C205/45 , A01N35/04 , C07C45/46 , C07C45/673 , C07C45/676 , C07C45/68 , C07C45/70 , C07C45/71 , C07C49/84 , C07C65/21 , C07C65/24
摘要： Substituted benzophenone compounds are disclosed, having the formula: ##STR1## The compounds are useful as fungicides having high systemicities.

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