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61. 发明授权

US07208169B2 Biphenyl carboxamides 有权
标题翻译：联苯甲酰胺
公开(公告)号：US07208169B2
公开(公告)日：2007-04-24
申请号：US10512706
申请日：2003-04-16
申请人： Ralf Dunkel , Hans-Ludwig Elbe , Heiko Rieck , Robert Markert , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck , Martin Kugler , Thomas Jaetsch
发明人： Ralf Dunkel , Hans-Ludwig Elbe , Heiko Rieck , Robert Markert , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck , Martin Kugler , Thomas Jaetsch
IPC分类号： A01N25/00 , C07D241/00 , C07D241/02 , C07D419/00 , C07D405/00
CPC分类号： A01N43/30 , A01N43/32 , A01N43/56 , A01N43/78 , C07D317/58 , C07D319/20 , C07D405/12 , C07D407/12 , C07D409/12 , C07D417/12
摘要： The invention relates to novel biphenylcarboxamides of the formula (I) in which R1, R2, m, n, R3, Y and A are as defined in the disclosure, to a plurality of processes for preparing these substances and their use for controlling unwanted microorganisms, and to novel intermediates and their preparation.
摘要翻译：本发明涉及式（I）的新型联苯甲酰胺，其中R 1，R 2，m，n，R 3，Y和 A如本公开所定义，涉及制备这些物质的多种方法及其用于控制不需要的微生物的用途，以及新型中间体及其制备方法。

62. 发明申请

US20060148886A1 Methylthiophene carboxanilides 有权
标题翻译：甲基噻吩甲酰苯胺
公开(公告)号：US20060148886A1
公开(公告)日：2006-07-06
申请号：US10511742
申请日：2003-04-15
申请人： Ralf Dunkel , Heiko Rieck , Hans-Ludwig Elbe , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck
发明人： Ralf Dunkel , Heiko Rieck , Hans-Ludwig Elbe , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck
IPC分类号： A01N43/06 , C07D333/22
CPC分类号： A01N43/10 , C07D333/38
摘要： This invention relates to novel methylthiophenecarboxanilides of the formula (I) in which R1, R2, R3, R4, R5 and R6 are as defined in the disclosure, to a plurality of processes for preparing these substances and their use for controlling unwanted micro-organisms, and to novel intermediates and their preparations.
摘要翻译：本发明涉及式（I）的新的甲基噻吩甲酰苯胺，其中R 1，R 2，R 3，R 4，对于制备这些物质的多种方法及其用于控制不想要的微生物的方法，R 5和R 6如本公开所定义，以及以新颖的中间体及其制备方法。

63. 发明申请

US20050272785A1 Biphenyl carboxamides 有权
标题翻译：联苯甲酰胺
公开(公告)号：US20050272785A1
公开(公告)日：2005-12-08
申请号：US10512706
申请日：2003-04-16
申请人： Ralf Dunkel , Hans-Ludwig Elbe , Heiko Rieck , Robert Markert , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck , Martin Kugler , Thomas Jaetsch
发明人： Ralf Dunkel , Hans-Ludwig Elbe , Heiko Rieck , Robert Markert , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck , Martin Kugler , Thomas Jaetsch
IPC分类号： C07D317/62 , A01N43/30 , A01N43/32 , A01N43/56 , A01N43/78 , C07B61/00 , C07D317/58 , C07D319/20 , C07D405/12 , C07D407/12 , C07D409/12 , C07D417/12 , A61K31/427 , A61K31/381 , A61K31/4025 , C07D417/02 , C07D45/02 , C07D49/02
CPC分类号： A01N43/30 , A01N43/32 , A01N43/56 , A01N43/78 , C07D317/58 , C07D319/20 , C07D405/12 , C07D407/12 , C07D409/12 , C07D417/12
摘要： Novel biphenylcarboxamides of the formula (I) in which R1, R2, m, n, R3, Y and A are as defined in the description, a plurality of processes for preparing these substances and their use for controlling unwanted microorganisms, and also novel intermediates and their preparation.
摘要翻译：其中R 1，R 2，m，n，R 3，Y和A的式（I）的新型联苯基甲酰胺如上定义在描述中，制备这些物质的多种方法及其用于防治有害微生物的用途，以及新型中间体及其制备方法。

64. 发明申请

US20050222173A1 Triazolopyrimidines 审中-公开
标题翻译：三唑并嘧啶
公开(公告)号：US20050222173A1
公开(公告)日：2005-10-06
申请号：US10508402
申请日：2003-03-10
申请人： Christiane Boie , Ralf Dunkel , Hans-Ludwig Elbe , Herbert Gayer , Olaf Gebauer , Bernd-Wieland Kruger , Ulrich Heinemann , Arnd Voerste , Oliver Guth , Ronald Ebbert , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik
发明人： Christiane Boie , Ralf Dunkel , Hans-Ludwig Elbe , Herbert Gayer , Olaf Gebauer , Bernd-Wieland Kruger , Ulrich Heinemann , Arnd Voerste , Oliver Guth , Ronald Ebbert , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik
IPC分类号： A01N25/30 , A01N43/90 , C07D249/10 , C07D249/14 , C07D487/04 , A61K31/519 , C07D487/02
CPC分类号： C07D249/10 , C07D487/04
摘要： Novel triazolopyrimidines of the formula in which R1 represents amino, represents in each case optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, alkylamino, dialkylamino, alkenylamino, alkynylamino, cycloalkylamino, N-cycloalkyl-N-alkylamino, alkylideneamino or heterocyclyl, and R2 represents hydrogen or represents in each case optionally substituted alkyl, alkenyl, alkynyl or cycloalkyl, or R1 and R2 together with the nitrogen atom to which they are attached form an optionally substituted heterocyclic ring, R3 represents aryl which is optionally mono- to tetrasubstituted, R4 represents halogen, cyano or represents in each case optionally substituted alkoxy or dialkylamino and X represents halogen, a process for preparing these novel substances and their use for controlling unwanted microorganisms. Novel intermediates of the formulae and processes for their preparation.
摘要翻译：其中R 1表示氨基的新型三唑并嘧啶代表在每种情况下为任选取代的烷基，烯基，炔基，环烷基，烷氧基，烯氧基，炔氧基，环烷氧基，烷基氨基，二烷基氨基，烯基氨基，炔基氨基，环烷基氨基，N-环烷基-N-烷基氨基，亚烷基氨基或杂环基，R 2表示氢或在各种情况下表示任选取代的烷基，烯基，炔基或环烷基，或R 1， R 2和它们所连接的氮原子一起形成任选取代的杂环，R 3表示任选被单取代至四取代的芳基， 4代表卤素，氰基或在每种情况下代表任选取代的烷氧基或二烷基氨基，X代表卤素，制备这些新物质的方法及其用于控制不想要的微生物的用途。新型中间体的配方及其制备方法。

65. 发明申请

US20050182120A1 Pyrazolyl biphenyl carboxamides and the use thereof for controlling undesirable microorganisms 失效
标题翻译：吡唑基联苯甲酰胺及其用于控制不期望的微生物的用途
公开(公告)号：US20050182120A1
公开(公告)日：2005-08-18
申请号：US11050306
申请日：2005-02-02
申请人： Hans-Ludwig Elbe , Heiko Rieck , Ralf Dunkel , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck , Martin Kugler , Thomas Jaetsch
发明人： Hans-Ludwig Elbe , Heiko Rieck , Ralf Dunkel , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck , Martin Kugler , Thomas Jaetsch
IPC分类号： A01N43/56 , A61K31/4155 , A61K31/4439 , A61P31/00 , C07B61/00 , C07C45/68 , C07C47/546 , C07C223/06 , C07C249/12 , C07C251/48 , C07D213/30 , C07D231/16 , C07D401/12 , C07F5/02 , A01N43/40 , A01N41/02 , C07D231/14 , C07D43/02
CPC分类号： C07D213/30 , C07C223/06 , C07C251/48 , C07D231/16 , C07D401/12
摘要： Novel pyrazolylbiphenylcarboxamides of the formula (I) in which R1, R2, X, m, Y and n are each as defined in the description, a plurality of processes for preparing these substances and their use for controlling undesirable microorganisms, and also novel intermediates and their preparation.
摘要翻译：其中R 1，R 2，X，m，Y和n各自如说明书中所定义的式（I）的新型吡唑基联苯甲酰胺，制备这些物质及其用于控制不良微生物的用途，以及新型中间体及其制备方法。

66. 发明申请

US20050009703A1 Fungicidal active substance combinations containing trifloxystrobin 有权
标题翻译：含有肟菌酯的杀真菌活性物质组合
公开(公告)号：US20050009703A1
公开(公告)日：2005-01-13
申请号：US10486663
申请日：2002-08-05
申请人： Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Christoph Erdelen , Angelika Lubos-Erdelen , Hirohisa Ohtake
发明人： Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Christoph Erdelen , Angelika Lubos-Erdelen , Hirohisa Ohtake
IPC分类号： A01N37/36 , A01N37/50 , A01N43/40 , A01N47/40 , A01N47/42 , A01N51/00 , A01N43/36 , A01N43/56 , A01N43/647 , A01N43/713 , A01N43/72
CPC分类号： A01N43/78 , A01N37/50 , A01N43/08 , A01N43/40 , A01N43/72 , A01N51/00 , A01N47/40 , A01N2300/00
摘要： The Present invention relates to novel active compound combinations comprising a known oxime ether derivative (trifloxystrobin) and imidacloprid, which combinations are highly suitable for controlling phytopathogenic fungi and insects.
摘要翻译：本发明涉及包含已知的肟醚衍生物（肟菌酯）和吡虫啉的新型活性化合物组合，其组合非常适用于防治植物病原真菌和昆虫。

67. 发明授权

US06294543B1 Plant protection agents 失效
标题翻译：植物保护剂
公开(公告)号：US06294543B1
公开(公告)日：2001-09-25
申请号：US09319550
申请日：1999-06-08
申请人： Paul Margot , Gertrude Knauf-Beiter , Astrid Mauler-Machnik
发明人： Paul Margot , Gertrude Knauf-Beiter , Astrid Mauler-Machnik
IPC分类号： A01N4354
CPC分类号： A01N37/50 , A01N43/82 , A01N43/76 , A01N43/54 , A01N43/42 , A01N43/36 , A01N43/30 , A01N37/24 , A01N2300/00
摘要： Microbicide composition for plants, containing at least two active ingredient components in an amount producing synergistic activity, together with an appropriate filler, characterised in that component I is the compound 2-[&agr;-{[(&agr;-methyl-3-trifluoromethyl-benzyl)imino]-oxy}-o-tolyl]-yoxylic acid-methylester-O-methyloxime, and component II is a compound selected from the group IIA) 5,7-dichloro-4-(4-fluorophenoxy)quinoline (“Quinoxyfen”); IIB) 4-cyclopropyl-methyl-N-phenyl-2-pyrimidinamine (“Cyprodinil”); IIC) benzo(1,2,3)thiadiazole-7-carbothio-acid-S-methylester (“Acibenzolar-S-methyl”); IID) 3-anilino-5methyl-5(4-phenoxyphenyl)-1,3-oxazolidine-2,4-ione (“Famoxadone”); IIE) 8-(1,1-dimethylethyl)-N-ethyl-N-propyl-1,4-dioxaspiro[4.5]decane-2-methanamine (“Spiroxamin”); IIF) 4-(2,2-difluoro-1,3-benzodioxol-4-yl)pyrrole-3-carbonitrile (“Fludioxonil”); IIG) 4-(2,3-dichlorophenyl)pyrrole-3-carbonitrile (“Fenpiclonil”); IIH) 1-methyl-cyclohexanecarboxylic acid-(2,3-dichloro-4-hydroxy-phenyl)-amide (“Fenhexamid”); IIJ) 2-{2-[6-(2-cyano-phenoxy)-pyrimidin-4-yloxy]-phenyl}-3-methoxy-acrylic acid methyl ester (“Azoxystrobin”); IIK) Methoximino-(2-o-tolyloxymethyl-phenyl)-acetic acid methyl ester (“Kresoxim-methyl”); or repectively one of the salts or metal complexes of components I and II.
摘要翻译：用于植物的杀微生物剂组合物，含有至少两种产生协同活性的量的活性成分组分以及合适的填料，其特征在于组分I是化合物2-β-{[（α-甲基-3-三氟甲基 - 苄基）亚氨基] - 氧基} - 对 - 甲苯基] - 甲氧基 - 甲基酯-O-甲基肟，组分II是选自ⅡA）5,7-二氯-4-（4-氟苯氧基）喹啉（“Quinoxyfen”）的化合物; IIB）4-环丙基 - 甲基-N-苯基-2-嘧啶胺（“Cyprodinil”）; IIC）苯并（1,2,3）噻二唑-7-硫代甲酸S-甲酯（“Acibenzolar-S- ）; IID）3-苯胺基-5-甲基-5（4-苯氧基苯基）-1,3-恶唑烷-2,4-离子（“Famoxadone”）; IIE）8-（1,1-二甲基乙基）-N-乙基 - N-丙基-1,4-二氧杂螺[4.5]癸烷-2-甲胺（“螺螺心”）; IIF）4-（2,2-二氟-1,3-苯并间二氧杂环戊烯-4-基）吡咯-3-甲腈 “二氯苯基”）; IIG）4-（2,3-二氯苯基）吡咯-3-腈（“Fenpiclonil”）; IIH）1-甲基 - 环己烷羧酸 - （2,3-二氯-4-羟基 - 苯基）一个酰胺（“Fenhexamid”）; IIJ）2- {2- [6-（2-氰基 - 苯氧基） - 嘧啶-4-基氧基] - 苯基} -3-甲氧基 - 丙烯酸甲酯（“Azoxystrobin”）; IIK ）肟基 - （2-邻甲苯氧基甲基 - 苯基） - 乙酸甲酯（“Kresoxim-methyl”）;或分别是组分I和II的盐或金属配合物之一。

68. 发明授权

US07538073B2 Pyrazoylcarboxanilides as fungicides 有权
标题翻译：吡唑烷酰苯胺作为杀真菌剂
公开(公告)号：US07538073B2
公开(公告)日：2009-05-26
申请号：US10484108
申请日：2002-07-12
申请人： Hans-Ludwig Elbe , Heiko Rieck , Ralf Dunkel , Qin Zhu-Ohlbach , Astrid Mauler-Machnik , Ulrike Wachendorff-Neumann , Karl-Heinz Kuck
发明人： Hans-Ludwig Elbe , Heiko Rieck , Ralf Dunkel , Qin Zhu-Ohlbach , Astrid Mauler-Machnik , Ulrike Wachendorff-Neumann , Karl-Heinz Kuck
IPC分类号： A01N43/56
CPC分类号： A01N43/56 , C07D231/16
摘要： The present invention relates to novel pyrazolylcarboxanilides of the formula (I) in which R1, R2, G, R3 and n are as defined in the disclosure, to a plurality of processes for preparing these substances and their use for controlling undesirable microorganisms and to novel intermediates and their preparation.
摘要翻译：本发明涉及式（I）的新的吡唑基甲酰苯胺，其中R1，R2，G，R3和n如本公开所定义，涉及制备这些物质的多种方法及其用于控制不期望的微生物和新颖的中间体及其制备。

69. 发明授权

US07348350B2 Pyrazolyl biphenyl carboxamides and the use thereof for controlling undesirable microorganisms 失效
标题翻译：吡唑基联苯甲酰胺及其用于控制不期望的微生物的用途
公开(公告)号：US07348350B2
公开(公告)日：2008-03-25
申请号：US11050306
申请日：2005-02-02
申请人： Hans-Ludwig Elbe , Heiko Rieck , Ralf Dunkel , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck , Martin Kugler , Thomas Jaetsch
发明人： Hans-Ludwig Elbe , Heiko Rieck , Ralf Dunkel , Ulrike Wachendorff-Neumann , Astrid Mauler-Machnik , Karl-Heinz Kuck , Martin Kugler , Thomas Jaetsch
IPC分类号： A01N43/56 , C07D231/18
CPC分类号： C07D213/30 , C07C223/06 , C07C251/48 , C07D231/16 , C07D401/12
摘要： Novel pyrazolylbiphenylcarboxamides of the formula (I) in which R1, R2, X, m, Y and n are each as defined in the description, a plurality of processes for preparing these substances and their use for controlling undesirable microorganisms, and also novel intermediates and their preparation.
摘要翻译：其中R 1，R 2，X，m，Y和n各自如说明书中所定义的式（I）的新型吡唑基联苯甲酰胺，制备这些物质及其用于控制不良微生物的用途，以及新型中间体及其制备方法。

70. 发明授权

US07189680B2 5-halo-6-aryl[1,2,4]triazolo[1,5-a]pyrimidin-7-amines 失效
标题翻译： 5-卤代-6-芳基[1,2,4]三唑并[1,5-a]嘧啶-7-胺
公开(公告)号：US07189680B2
公开(公告)日：2007-03-13
申请号：US10475317
申请日：2002-04-16
申请人： Olaf Gebauer , Jörg Nico Greul , Ulrich Heinemann , Hans-Ludwig Elbe , Bernd-Wieland Krüger , Ralf Dunkel , Arnd Voerste , Ronald Ebbert , Astrid Mauler-Machnik , Ulrike Wachendorff-Neumann , Karl-Heinz Kuck , Yoshinori Kitagawa
发明人： Olaf Gebauer , Jörg Nico Greul , Ulrich Heinemann , Hans-Ludwig Elbe , Bernd-Wieland Krüger , Ralf Dunkel , Arnd Voerste , Ronald Ebbert , Astrid Mauler-Machnik , Ulrike Wachendorff-Neumann , Karl-Heinz Kuck , Yoshinori Kitagawa
IPC分类号： A01N43/90 , C07D487/04 , C07C269/04
CPC分类号： C07D487/04 , A01N43/90 , A01N47/04 , A01N47/34 , C07C211/15 , C07C211/24 , C07C239/20 , C07C271/12 , C07C271/16
摘要： The invention relates to novel triazolopyrimidines of the formula in which R1, R2, R3 and X have the meanings given in the disclosure, and acid addition salts thereof, to a plurality of processes for preparing these novel substances, and to their use for controlling unwanted microorganisms. The invention further relates to novel amines and carbamates of the formulae indicated in the description and to processes for preparing these intermediates.
摘要翻译：本发明涉及下式的新型三唑并嘧啶，其中R 1，R 2，R 3和X具有本公开中给出的含义，及其酸加成盐，用于制备这些新物质的多种方法及其用于防治有害微生物的用途。本发明还涉及本说明书中指出的通式的新型胺和氨基甲酸酯以及这些中间体的制备方法。

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