Insecticidal arylpyrrolines 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
EP2432762 A1 2012-03-28 [EP2432762]EP2432762 B1 2015-02-25 [EP2432762]EP2432762 B8 2015-04-08 [EP2432762] / 2012-03-282015-02-252015-04-08
申请号/申请日
2010EP-0720721 / 2010-05-18
发明人
MURATA TETSUYA;YONETA YASUSHI;KISHIKAWA HIDETOSHI;MIHARA JUN;YAMAZAKI DAIEI;HATAZAWA MAMORU;SASAKI NORIO;DOMON KEI;SHIMOJO EIICHI;ICHIHARA TERUYUKI;SHIBUYA KATSUHIKO;ATAKA MASASHI;GÖRGENS ULRICH;
申请人
BAYER INTELLECTUAL PROPERTY;
主分类号
IPC分类号
A01N-043/36C07D-207/20C07D-401/04C07D-401/14C07D-403/10C07D-403/14
摘要
(EP2432762) The invention relates to novel arylpyrroline compounds of formula (I) which have excellent insecticidal activity and which can thus be used as an insecticide.
机翻摘要
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地址
代理人
代理机构
;
优先权号
2009JP-0121267 2009-05-19 2010WO-EP03019 2010-05-18
主权利要求
(EP2432762) 1. Arylpyrroline compounds of formula (I) (see diagramm) wherein Q stands for a 2-pyridyl group, a 3-pyridyl group, or a 4-pyridyl group which may be substituted by at least one substituent X or X **1; X and X **1 each independently stand for fluorine, chlorine, bromine, iodine, C 1-12haloalkyl, nitro, C 1-12alkyl, or C 1-12alkoxyl, cyano, C 1-12haloalkoxyl, C 1-12alkylsulfenyl, C 1-12alkylsulfinyl, C 1-12alkylsulfonyl, C 1-12haloalkylsulfenyl, C 1-12haloalkylsulfinyl, or C 1-12haloalkylsulfonyl, hydroxyl, thiol, amino, C 1-12acylamino, C 1-12alkoxy-carbonylamino, C 1-12haloalkoxycarbonylamino, C 1-12alkoxyimino, C 1-12haloalkoxyimino, or C 1-12alkylsulfonylamino, or sulfur pentafluoride; A **1, A **2, A **3 and A **4 each independently stand for a carbon atom which may be substituted by a substituent Y, and whereas two adjacent substituents Y together with the carbon atoms to which they are attached may form a 5- or 6-membered aromatic ring, or A **1, A **2, A **3 and A **4 each independently stand for a nitrogen atom, under the proviso that only 2 of the chemical groups A **1, A **2, A **3 and A **4 stand at the same time for nitrogen; Y stands for fluorine, chlorine, bromine, iodine, C 1-12haloalkyl, nitro, C 1-12alkyl, C 3-8cycloalkyl, C 3-8cyclohaloalkyl, C 1-12alkoxyl, cyano, C 1-12haloalkoxyl, C 1-12alkylsulfenyl, C 1-12alkylsulfinyl, C 1-12alkylsulfonyl, C 1-12haloalkylsulfenyl, C 1-12haloalkylsulfinyl, C 1-12haloalkylsulfonyl, C 1-12alkylsulfonyloxy, C 1-12haloalkylsulfonyloxy, C 1-12alkylaminosulfonyl, C 1-12haloalkylaminosulfonyl, di(C 1-12)alkylaminosulfonyl, or di((C 1-12haloalkyl)aminosulfonyl, hydroxyl, thiol, amino, C 1-12alkylamino, di(C 1-12)alkylamino, C 1-12acylamino, C 1-12alkoxycarbonylamino, C 1-12haloalkoxycarbonylamino, C 1-12alkylsulfonylamino, C 1-12haloalkylsulfonylamino, C 1-12trialkylsilyl, C 1-12alkoxyimino, C 1-12 haloalkoxyimino, C 1-12alkoxyiminoalkyl, C 1-12haloalkoxyimino(C 1-12)alkyl, C 1-12alkylsulfinylimino, C 1-12alkylsulfinylimino(C 1-12)alkyl, C 1-12alkylsulfinylimino(C 1-12)alkylcarbonyl, C 1-12alkylsulfoxyimino, C 1-12alkylsulfoxyimino(C 1-12)alkyl, C 1-12alkoxycarbonyl, C 1-12alkylcarbonyl, aminocarbonyl, C 1-12alkylaminocarbonyl, aminothiocarbonyl, C 1-12alkylaminothiocarbonyl, di(C 1-12)alkylaminocarbonyl, or di(C 1-12)alkylaminothiocarbonyl; G stands for a heterocyclic group G1 to G9 having the following formula (see diagramm) which may be substituted by a substituent Z which is selected among fluorine, chlorine, bromine, iodine, C 1-6 haloalkyl, nitro, C 1-6alkoxy, cyano, C 1-6haloalkoxy, C 1-6alkylsulfenyl, C 1-6alkylsulfinyl, C 1-6alkylsulfonyl, C 1-6haloalkylsulfenyl, C 1-6haloalkylsulfinyl, C 1-6haloalkylsulfonyl, hydroxyl and thiol,  or represents a chemical group G10 characterized by the following formula: (see diagramm) wherein R **1 and R **2 each independently stand for hydrogen, C 1-12alkyl, C 3-8cycloalkyl, C 1-12haloalkyl, C 3-8cyclohaloalkyl, C 2-12alkenyl, C 2-12alkynyl, C 2-12haloalkenyl, C 2-12haloalkynyl, cyano, C 1-12alkoxycarbonyl, or C 1-12 alkoxythiocarbonyl, or R **1 and R **2, together with the carbon atom to which they are attached, form a 3 to 6-membered carbocyclic ring; R **3 represents hydrogen, amino, hydroxyl, C 1-12alkoxy, C 1-12alkylcarbonylamino, C 1-12alkylimino, C 1-12alkyl, C 3-8cycloalkyl, or C 1-12haloalkyl, cyano, or C 2-12alkenyl, C 2-12alkynyl, or C 1-12alkylcarbonyl, or is selected from the following groups CH 2-R **5,C(=O)R **5, C(=S)R **5, R **4 represents a chemical group selected among hydrogen, cyano, C 1-12alkylcarbonyl, C 1-12alkylthiocarbonyl, C 1-12haloalkylcarbonyl, C 1-12haloalkylthiocarbonyl, C 1-12 alkylaminocarbonyl, C 1-12alkylaminothiocarbonyl, di(C 1-12)alkylaminocarbonyl, di(C 1-12)alkyl-aminothiocarbonyl, C 1-12alkoxyaminocarbonyl, C 1-12alkoxyaminothiocarbonyl, C 1-12alkoxycarbonyl,  C 1-12alkoxythiocarbonyl, C 1-12thioalkoxycarbonyl, C 1-12thioalkoxythiocarbonyl, C 1-12alkylsulfonyl,  C 1-12haloalkylsulfonyl, C 3-8cycloalkylcarbonyl, C 2-12alkenylcarbonyl, C 2-12alkynylcarbonyl, C 3-8cycloalkyl-(C 1-12)alkylcarbonyl, C 1-12alkylsulfonyl(C 1-12)alkylcarbonyl, C 1-12alkylsulfinyl(C 1-12)alkylcarbonyl, C 1-12alkylsulfonyl(C 1-12)alkylcarbonyl, C 1-12alkylcarbonyl(C 1-12)alkylcarbonyl, C 3-8cycloalkylaminocarbonyl, C 2-12 alkenylaminocarbonyl, C 2-12alkynylaminocarbonyl, C 1-12alkoxy(C 1-12)alkyl, or is selected from the groups C(=O)R **5 and C(=S)R **5, or R **3 and R **4, together with the nitrogen atom to which they are bound, form a 3- to 6-membered heterocyclic ring which may be substituted with a substituent X or X **1, or may be substituted with a keto, thioketo or nitroimino group; and R **5 represents optionally substituted phenyl, or an optionally substituted heterocyclic ring. 2. Arylpyrroline compounds according to claim 1, wherein in formula (I) the grouping (see diagramm) stands for a grouping selected among P1 to P4 (see diagramm) wherein Y is as defined herein, and k stands for 0, 1, 2, 3 or 4. 3. Composition, comprising at least one compound according to any one of claims 1 or 2 for controlling animal pests. 4. Use of at least one compound according to any one of claims 1 or 2 for preparing compositions for controlling arthropods. 5. Use of compounds according to any one of claims 1 or 2 for treating seed of conventional or transgenic plants. 6. Compounds according to any one of claims 1 or 2 for use against animal parasitic pests 7. Compounds according to any one of claims 1 or 2 for use for controlling arthropods which attack animals.
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code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=SE  MEMBER STATE LEGAL DETAILS FOR SI  Actual or expected expiration date=2016-02-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=SI     Event publication date=2016-02-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=SI  MEMBER STATE LEGAL 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EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member sta(...)
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