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1. 发明申请

US20130065922A1 NOVEL AMIDES AS FUNGICIDES 审中-公开
标题翻译：新陈代谢作为防腐剂
公开(公告)号：US20130065922A1
公开(公告)日：2013-03-14
申请号：US13699619
申请日：2011-05-04
申请人： Stephan Trah , Laura Quaranta , Renaud Beaudegnies , Fiona Murphy Kessabi , Guillaume Berthon , Clemens Lamberth
发明人： Stephan Trah , Laura Quaranta , Renaud Beaudegnies , Fiona Murphy Kessabi , Guillaume Berthon , Clemens Lamberth
IPC分类号： C07D215/36 , A01N43/42 , A01P3/00 , C07D215/20
CPC分类号： C07D213/30 , C07D213/32
摘要： Compounds of the general formula (I), wherein the substituents are as defined in claim 1, are useful as fungicides.
摘要翻译：通式（I）的化合物，其中取代基如权利要求1中所定义，可用作杀真菌剂。

2. 发明申请

US20130096156A1 QUINOLINE DERIVATIVES AS FUNGICIDES 审中-公开
标题翻译：喹啉衍生物作为防腐剂
公开(公告)号：US20130096156A1
公开(公告)日：2013-04-18
申请号：US13703340
申请日：2011-05-23
申请人： Laura Quaranta , Stephan Trah , Renaud Beaudegnies , Fiona Murphy Kessabi , Guillaume Berthon , Clemens Lamberth
发明人： Laura Quaranta , Stephan Trah , Renaud Beaudegnies , Fiona Murphy Kessabi , Guillaume Berthon , Clemens Lamberth
IPC分类号： A01N43/42 , C07D215/20
CPC分类号： A01N43/42 , C07D215/18 , C07D215/20
摘要： Compounds of the general formula (I) wherein the substituents are as defined in claim 1, are useful as fungicides.
摘要翻译：其中取代基如权利要求1中所定义的通式（I）的化合物可用作杀真菌剂。

3. 发明申请

US20140045890A1 NOVEL COMPOUNDS 审中-公开
标题翻译：新型化合物
公开(公告)号：US20140045890A1
公开(公告)日：2014-02-13
申请号：US14007355
申请日：2012-03-28
申请人： Guillaume Berthon , Fiona Kessabi Murphy , Renaud Beaudegnies , Clemens Lamberth , Laura Quaranta , Stephan Trah
发明人： Guillaume Berthon , Fiona Kessabi Murphy , Renaud Beaudegnies , Clemens Lamberth , Laura Quaranta , Stephan Trah
IPC分类号： A01N43/80 , A01N43/42
CPC分类号： A01N43/80 , A01N43/42 , A01N43/78 , C07D401/12 , C07D409/14 , C07D413/12 , C07D417/12
摘要： Compounds of the general formula (I) wherein the substituents are as defined in claim 1, are useful as fungicides.
摘要翻译：其中取代基如权利要求1中所定义的通式（I）的化合物可用作杀真菌剂。

4. 发明申请

US20130281467A1 NOVEL MICROBICIDES 审中-公开
标题翻译：新型微生物
公开(公告)号：US20130281467A1
公开(公告)日：2013-10-24
申请号：US13881648
申请日：2011-10-28
申请人： Stephan Trah , Laura Quaranta , Clemens Lamberth , Martin Pouliot
发明人： Stephan Trah , Laura Quaranta , Clemens Lamberth , Martin Pouliot
IPC分类号： A01N43/54 , A01N43/90
CPC分类号： A01N43/54 , A01N43/90 , C07D401/04 , C07D491/04 , C07D491/10
摘要： Compounds of formula (I), wherein G represents together with the two carbon atoms of the pyrimidine ring to which it is attached, a 5- to 7-membered aliphatic carbocyclic or heterocyclic ring system which contain 0 to 2 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur; and wherein said 5- to 7-membered aliphatic carbocyclic or heterocyclic ring system can be mono-, di- or trisubstituted by substituents selected from the group consisting of halogen, keto, C1-C6alkyl, C1-C6alkoxy, C1-C6alkyloximino and C1-C6alkylendioxy; and wherein the other substituents R1, R2, R3, R4, R5 and R6 are as defined in claim 1, and their use as microbicides.
摘要翻译：式（I）化合物，其中G代表与其连接的嘧啶环的两个碳原子一起，含有0至2个选自以下的杂原子的5-至7-元脂族碳环或杂环系：的氮，氧和硫; 并且其中所述5-至7-元脂族碳环或杂环系统可以被选自卤素，酮，C 1 -C 6烷基，C 1 -C 6烷氧基，C 1 -C 6烷氧基肟基和C 1 -C 6烷氧基的取代基单，二或三取代， C6烷基二氧基; 并且其中其它取代基R 1，R 2，R 3，R 4，R 5和R 6如权利要求1中所定义，及其作为杀微生物剂的用途。

5. 发明申请

US20100273804A1 PYRIDAZINE DERIVATIVES USEFUL AS FUNGICIDES AND FOR THE TREATMENT OF CANCER 审中-公开
标题翻译：用作杀真菌剂和治疗癌症的吡咯烷酮衍生物
公开(公告)号：US20100273804A1
公开(公告)日：2010-10-28
申请号：US12809604
申请日：2008-12-19
申请人： Clemens Lamberth , Stephan Trah , Raphael Dumeunier , Sebastian Volker Wendeborn
发明人： Clemens Lamberth , Stephan Trah , Raphael Dumeunier , Sebastian Volker Wendeborn
IPC分类号： A61K31/501 , A01N43/58 , C07D403/04 , C07D237/08 , A01P3/00 , A61K31/50 , A61P35/00
CPC分类号： C07D237/12 , A01N43/58 , C07D237/14
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: formula (I) wherein R1 is C1-C6alkyl, C1-C6haloalkyl or C3-C6cycloalkyl; R2 is hydrogen or an optionally substituted alkyl, aryl or heteroaryl; R3 is hydrogen, C1-C6alkyl or C1-C6haloalkyl; R4 is hydrogen, C1-C6alkyl or C1-C6haloalkyl; or R3 and R4 together can be part of a carbocyclic or heterocyclic 3- to 8-membered ring; R5 is optionally substituted aryl or heteroaryl; and R6 is hydroxy, halogen, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylthio or C1-C6haloalkylthio; or an agrochemically usable salt form thereof.
摘要翻译：本发明涉及具有杀微生物活性，特别是杀真菌活性的作为活性成分的式（I）的新哒嗪衍生物：式（I）其中R 1是C 1 -C 6烷基，C 1 -C 6卤代烷基或C 3 -C 6环烷基; R 2是氢或任选取代的烷基，芳基或杂芳基; R3是氢，C1-C6烷基或C1-C6卤代烷基; R4是氢，C1-C6烷基或C1-C6卤代烷基; 或者R 3和R 4一起可以是碳环或杂环的3至8元环的一部分; R5是任选取代的芳基或杂芳基; R 6为羟基，卤素，C 1 -C 6烷氧基，C 1 -C 6卤代烷氧基，C 1 -C 6烷硫基或C 1 -C 6卤代烷硫基; 或其农业化学上可用的盐形式。

6. 发明申请

US20110142802A1 FUNGICIDAL COMPOSITIONS 审中-公开
标题翻译：杀真菌剂
公开(公告)号：US20110142802A1
公开(公告)日：2011-06-16
申请号：US12863372
申请日：2009-01-14
申请人： Jeremy R. Godwin , Stephan Trah , Clemens Lamberth , Raphael Dumeunier , Valeria Grasso , Sebastian Volker Wendeborn
发明人： Jeremy R. Godwin , Stephan Trah , Clemens Lamberth , Raphael Dumeunier , Valeria Grasso , Sebastian Volker Wendeborn
IPC分类号： A01N63/04 , A01N59/26 , A01N59/20 , A01N59/18 , A01N59/16 , A01N59/00 , A01N65/26 , A01N65/08 , A01N43/16 , A01N57/20 , A01N37/18 , A01N43/62 , A01N43/88 , A01N43/58 , A01N43/90 , A01P3/00
CPC分类号： A01N43/58 , A01N37/34 , A01N43/54 , A01N43/653 , A01N47/14 , A01N51/00 , A01N2300/00
摘要： A fungicidal composition suitable for control of disease caused by phytopathogens comprising (A) a compound of formula (I), wherein R1 is methyl, ethyl or isopropyl; R2 is 2-chloro-6-fluoro-phenyl, 2,4,6-trifluorophenyl or 2,6-difluoro-4-methoxy-phenyl; R3 is chloro, fluoro or methoxy; and (B) a compound selected, for example, from the group consisting of (B1) a strobilurin fungicide, (B2) an azole fungicide, (B3) a morpholine fungicide, and (B4) an anilinopyrimidine fungicide.
摘要翻译：一种适于控制由植物病原体引起的疾病的杀真菌组合物，其包含（A）式（I）化合物，其中R 1为甲基，乙基或异丙基; R2是2-氯-6-氟 - 苯基，2,4,6-三氟苯基或2,6-二氟-4-甲氧基 - 苯基; R3是氯，氟或甲氧基; 和（B）选自例如（B1）嗜球果伞素杀真菌剂，（B2）唑类杀真菌剂，（B3）吗啉杀真菌剂和（B4）苯胺基嘧啶杀真菌剂的组合的化合物。

7. 发明申请

US20100144674A1 PYRIDAZINE DERIVATIVES 审中-公开
标题翻译：吡啶衍生物
公开(公告)号：US20100144674A1
公开(公告)日：2010-06-10
申请号：US12447028
申请日：2007-10-23
申请人： Stephan Trah , Clemens Lamberth , Sebastian Wendeborn
发明人： Stephan Trah , Clemens Lamberth , Sebastian Wendeborn
IPC分类号： A01N57/00 , C07D237/02 , A01N43/58 , A01N43/54 , A01N43/84 , A01P3/00 , A01P15/00
CPC分类号： C07D237/14 , A01N43/58 , C07D237/08 , C07D237/12 , C07D307/60 , C07D307/79 , C07D401/04 , C07D401/12 , C07D403/04 , C07D405/04 , C07D405/12 , C07D407/04 , C07D409/04 , C07D409/12 , C07D413/04 , C07D417/04
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R1 is hydrogen, C1-C6alkyl, C1-C8haloalkyl or C3-C6cycloalkyl; R2 is cycloalkyl, cycloalkylalkyl, halocycloalkyl, cycloalkoxy, halocycloalkoxy, cycloalkylalkoxy, halocycloalkylalkoxy, alkoxyalkyl, cycloalkoxyalkoxyalkyl, haloalkoxyalkyl, trialkylsilyl, alkylthioalkyl, haloalkylthioalkyl, cycloalkylthio, halocycloalkylthio, cycloalkylalkylthio, halocycloalkylalkylthio, alkylsulfinylalkyl, alkylsulfonylalkyl, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, C2-C6alkenyl, C2-C6alkynyl, optionally substituted arylsulfonyl, optionally substituted aryloxy, optionally optionally substituted heteroaryloxy, optionally substituted arylthio, optionally substituted heteroarylthio; or R2 together with an adjacent carbon atom forms an optionally substituted fused ring; R3 is an optionally substituted aryl; R4 is hydrogen, halogen, C1-C6alkyl, C1-C6haloalkyl, C1-C8alkoxy, C1-C6haloalkoxy, hydroxy or cyano; and n is a whole number from 1 to 4; or an agrochemically usable salt form thereof.
摘要翻译：本发明涉及具有杀微生物活性，特别是杀真菌活性的活性成分的式（I）的新哒嗪衍生物，其中R1是氢，C1-C6烷基，C1-C8卤代烷基或C3-C6环烷基; R 2是环烷基，环烷基烷基，卤代环烷基，环烷氧基，卤代环烷氧基，环烷基烷氧基，卤代环烷基烷氧基，烷氧基烷基，环烷氧基烷氧基烷基，卤代烷氧基烷基，三烷基甲硅烷基，烷硫基烷基，卤代烷硫基烷基，环烷硫基，卤代环烷硫基，环烷基烷硫基，卤代环烷基烷硫基，烷基亚磺酰基烷基，烷基磺酰基烷基，烷基亚磺酰基，卤代烷基亚磺酰基，烷基磺酰基，卤代烷基磺酰基， C 6链烯基，C 2 -C 6炔基，任选取代的芳基磺酰基，任选取代的芳氧基，任选任选取代的杂芳氧基，任选取代的芳硫基，任选取代的杂芳硫基; 或R 2与相邻的碳原子一起形成任选取代的稠环; R3是任选取代的芳基; R4是氢，卤素，C1-C6烷基，C1-C6卤代烷基，C1-C8烷氧基，C1-C6卤代烷氧基，羟基或氰基; n为1〜4的整数; 或其农业化学上可用的盐形式。

8. 发明申请

US20110112108A1 PYRIDAZINE FUNGICIDES 失效
标题翻译：吡咯烷类杀真菌剂
公开(公告)号：US20110112108A1
公开(公告)日：2011-05-12
申请号：US12863377
申请日：2009-01-14
申请人： Stephan Trah , Clemens Lamberth , Raphael Dumeunier , Sebastian Volker Wenderborn
发明人： Stephan Trah , Clemens Lamberth , Raphael Dumeunier , Sebastian Volker Wenderborn
IPC分类号： A61K31/501 , C07D401/04 , A01N43/48 , A61P35/00 , A01P3/00
CPC分类号： C07D401/04
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R1 is methyl, ethyl or isopropyl; R2 is chloro, fluoro, hydroxy or C1-C2alkoxy; R3 is H, chloro, fluoro, methoxy or C1-C3alkyl; R4 is chloro, fluoro or bromo; and R3 is H, fluoro or methoxy; or an agrochemically usable salt form thereof; with the proviso that when R1 is methyl, R2 is chloro and R3 is H, then R4 or R5 is different from fluoro.
摘要翻译：本发明涉及式（I）的新的哒嗪衍生物作为具有杀微生物活性的活性成分，特别是杀真菌活性：其中R1是甲基，乙基或异丙基; R2是氯，氟，羟基或C1-C2烷氧基; R3是H，氯，氟，甲氧基或C1-C3烷基; R4是氯，氟或溴; 且R 3为H，氟或甲氧基; 或其农业化学可用的盐形式; 条件是当R 1为甲基时，R 2为氯且R 3为H，则R 4或R 5不同于氟。

9. 发明申请

US20100029668A1 NOVEL PYRIDAZINE DERIVATIVES 审中-公开
标题翻译：新的吡咯烷酮衍生物
公开(公告)号：US20100029668A1
公开(公告)日：2010-02-04
申请号：US12374052
申请日：2007-07-16
申请人： Stephan Trah , Clemens Lamberth , Sebastian Volker Wendeborn
发明人： Stephan Trah , Clemens Lamberth , Sebastian Volker Wendeborn
IPC分类号： A01N43/58 , C07D405/04 , A01P3/00
CPC分类号： C07D401/14 , A01N43/58 , C07D403/14 , C07D405/14 , C07D407/14 , C07D409/14 , C07D417/14
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R1 is hydrogen, C1-C6alkyl, C1-C6haloalkyl or C3-C6cycloalkyl; R2 is an optionally substituted heteroaryl; R3 is an optionally substituted heteroaryl; and R4 is hydrogen, halogen, C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, hydroxy or cyano; or an agrochemically usable salt form thereof.
摘要翻译：本发明涉及具有杀微生物活性，特别是杀真菌活性的活性成分的式（I）的新哒嗪衍生物，其中R1是氢，C1-C6烷基，C1-C6卤代烷基或C3-C6环烷基; R2是任选取代的杂芳基; R3是任选取代的杂芳基; R4是氢，卤素，C1-C6烷基，C1-C6卤代烷基，C1-C6烷氧基，C1-C6卤代烷氧基，羟基或氰基; 或其农业化学上可用的盐形式。

10. 发明授权

US08658644B2 Pyridazine derivatives, processes for their preparation and their use as fungicides 失效
标题翻译：哒嗪衍生物，其制备方法及其作为杀真菌剂的用途
公开(公告)号：US08658644B2
公开(公告)日：2014-02-25
申请号：US13576945
申请日：2011-02-01
申请人： Stephan Trah , Clemens Lamberth
发明人： Stephan Trah , Clemens Lamberth
IPC分类号： C07D237/08 , C07D237/12 , C07D237/14 , A61K31/50
CPC分类号： C07D237/12 , A01N43/58 , C07D237/14 , C07D307/58 , C07D307/60
摘要： The present invention relates to novel pyridazine derivatives of formula (I) wherein R1 is methyl or ethyl; R2 is H or chloro; R3 is fluoro or chloro; R4 is fluoro or methoxy; and R5 is chloro or methoxy or an agrochemically usable salt from thereof, as active ingredients which have microbiodidal activity, in particular fungicidal activity.
摘要翻译：本发明涉及式（I）的新的哒嗪衍生物，其中R 1是甲基或乙基; R2是H或氯; R3是氟或氯; R4是氟或甲氧基; R5为氯或甲氧基或其农药可用盐，作为具有微生物活性的活性成分，特别是杀真菌活性。

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