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1. 发明授权

US07491729B2 3-Substituted 3,4-dihydro-thieno[2,3-d]pyrimidin-4-one derivatives, production and use thereof 有权
标题翻译： 3-取代的3,4-二氢 - 噻吩并[2,3-d]嘧啶-4-酮衍生物，的制备和用途
公开(公告)号：US07491729B2
公开(公告)日：2009-02-17
申请号：US10539708
申请日：2003-12-17
申请人： Margaretha Bakker , Wilfried Hornberger , Andreas Kling , Udo Lange , Helmut Mack , Achim Moeller , Reinhold Mueller , Kurt Schellhaas , Martin Schmidt , Gerd Steiner , Karsten Wicke
发明人： Margaretha Bakker , Wilfried Hornberger , Andreas Kling , Udo Lange , Helmut Mack , Achim Moeller , Reinhold Mueller , Kurt Schellhaas , Martin Schmidt , Gerd Steiner , Karsten Wicke
IPC分类号： A01N43/54 , A61K31/505 , C07D239/00 , C07D471/00 , C07D487/00 , C07D491/00
CPC分类号： C07D495/14
摘要： 3-Substituted 3,4-dihydrothieno[2,3-d]pyrimidin-4-one derivatives, production and use thereof. The invention relates to 3,4-dihydrothieno[2,3-d]pyrimidin-4-one derivatives which are substituted in position 3 by 5-membered heteroaryl which may be fused to an aryl or heteroaryl radical, where the heteroaryl and, if appropriate, the fused aryl or heteroaryl radical may have 1, 2 or 3 substituents selected independently of one another from C1-5-alkyl, C1-5-alkoxy, C1-5-alkylthio, halogen, CN, halo-C1-5-alkyl, halo-C1-5-alkoxy, hydroxy, —NH2, —N(R6)2, —NH(R6), aryl, aryloxy, aralkyl, aralkyloxy and heteroaryl, where the substituents aryl, aryloxy, aralkyl, aralkyloxy and heteroaryl may have 1, 2 or 3 substituents selected independently of one another from C1-5-alkyl, C1-5-alkoxy, C1-5-alkylthio, halogen, CN, halo-C1-5-alkyl, halo-C1-5-alkoxy, hydroxy, —NH2, —N(R6)2 and —NH(R6). The preparation and use of these derivatives, especially for therapeutic purposes, e.g. for the treatment of depressions, are likewise described.
摘要翻译： 3-取代的3,4-二氢噻吩并[2,3-d]嘧啶-4-酮衍生物，的制备和用途。本发明涉及在3位被5位杂芳基取代的3,4-二氢噻吩并[2,3-d]嘧啶-4-酮衍生物，其可以与芳基或杂芳基稠合，其中杂芳基和稠合的芳基或杂芳基可以具有1,2或3个彼此独立地选自C 1-5 - 烷基，C 1-5 - 烷氧基，C 1-5 - 烷硫基，卤素，CN，卤代-C 1-5 - 烷基，卤代C 1-5 - 烷氧基，羟基，-NH 2，-N（R 6）2，-NH（R 6），芳基，芳氧基，芳烷基，芳烷氧基和杂芳基，其中芳基，芳氧基，芳烷基，芳烷氧基和杂芳基可以具有1,2或3个彼此独立地选自C 1-5 - 烷基，C 1-5 - 烷氧基，C 1-5 - 烷硫基，卤素，CN，卤代C 1-5 - 烷基，卤代-C 1-5 - 烷氧基，羟基，-NH 2，-N（R 6）2和-NH（R 6）。这些衍生物的制备和使用，特别是用于治疗目的，例如为了处理凹陷，同样地描述。

2. 发明申请

US20060142317A1 3-Substituted 3,4-dihydro-thieno[2,3-d]pyrimidin-4-one derivatives, production and use thereof 有权
标题翻译： 3-取代的3,4-二氢 - 噻吩并[2,3-d]嘧啶-4-酮衍生物，的制备和用途
公开(公告)号：US20060142317A1
公开(公告)日：2006-06-29
申请号：US10539708
申请日：2003-12-17
申请人： Margaretha Bakker , Wilfried Hornberger , Andreas Kling , Udo Lange , Helmut Mack , Achim Moeller , Reinhold Mueller , Kurt Schelhaas , Martin Schmidt , Gerd Steiner , Karsten Wicke
发明人： Margaretha Bakker , Wilfried Hornberger , Andreas Kling , Udo Lange , Helmut Mack , Achim Moeller , Reinhold Mueller , Kurt Schelhaas , Martin Schmidt , Gerd Steiner , Karsten Wicke
IPC分类号： A61K31/519 , C07D498/14
CPC分类号： C07D495/14
摘要： The invention relates to 3,4-dihydro-thieno[2,3-d]pyrimidin-4-one derivatives which are substituted in position 3 by 5-membered heteroaryl which may be fused to an aryl or heteroaryl radical, where the heteroaryl and, if appropriate, the fused aryl or heteroaryl radical may have 1, 2 or 3 substituents selected independently of one another from C1-5-alkyl, C1-5-alkoxy, C1-5-alkylthio, halogen, CN, halo-C1-5-alkyl, halo-C1-5-alkoxy, hydroxy, —NH2, —N(R6)2, —NH(R6), aryl, aryloxy, aralkyl, aralkyloxy and heteroaryl, where the substituents aryl, aryloxy, aralkyl, aralkyloxy and heteroaryl may have 1, 2 or 3 substituents selected independently of one another from C1-5-alkyl, C1-5-alkoxy, C1-5-alkylthio, halogen, CN, halo-C1-5-alkyl, halo-C1-5-alkoxy, hydroxy, —NH2, —N(R6)2 and —NH(R6). The preparation and use of these derivatives, especially for therapeutic purposes, e.g. for the treatment of depressions, are likewise described.
摘要翻译：本发明涉及在3位被5元杂芳基取代的3,4-二氢 - 噻吩并[2,3-d]嘧啶-4-酮衍生物，其可以与芳基或杂芳基稠合，其中杂芳基和如果合适，稠合的芳基或杂芳基可以具有1,2或3个彼此独立地选自C 1-5 - 烷基，C 1-5 - 烷氧基，C 1-5 - 烷硫基，卤素，CN，卤代-C 1-5 - 烷基，卤代C 1-5 - 烷氧基，羟基，-NH 2，-N（R 6）2，-NH（R 6），芳基，芳氧基，芳烷基，芳烷氧基和杂芳基，其中取代基芳基，芳氧基，芳烷基，芳烷氧基和杂芳基可以具有1,2或3个选自C 1-5 - 烷基，C 1-5 - 烷氧基，C 卤代C 1 -C 5烷基，卤素，CN，卤代-C 1-5烷基，卤代-C 1-5烷氧基，羟基，-NH 2，-N（R 6）2和-NH（R 6）。这些衍生物的制备和使用，特别是用于治疗目的，例如为了处理凹陷，同样地描述。

3. 发明授权

US06159962A 3-substituted 3,4-dihydro-thieno[2,3-D]pyrimidine derivatives and production and use of the same 有权
标题翻译： 3-取代的3,4-二氢 - 噻吩并[2,3-D]嘧啶衍生物及其制备和应用
公开(公告)号：US06159962A
公开(公告)日：2000-12-12
申请号：US445222
申请日：1999-12-06
申请人： Gerd Steiner , Uta Dullweber , Dorothea Starck , Alfred Bach , Karsten Wicke , Hans-Jurgen Teschendorf , Francisco-Javier Garcia-Ladona , Franz Emling
发明人： Gerd Steiner , Uta Dullweber , Dorothea Starck , Alfred Bach , Karsten Wicke , Hans-Jurgen Teschendorf , Francisco-Javier Garcia-Ladona , Franz Emling
IPC分类号： A61K31/519 , A61P25/00 , A61P25/24 , A61P43/00 , C07D495/04 , C07D417/06 , A61K31/551 , A61K31/559 , C07D417/14
CPC分类号： C07D495/04
摘要： 3-Substituted 3,4-dihydrothieno[2,3-d]pyrimidine derivatives of the formula I ##STR1## where R.sup.1 and R.sup.2 are a hydrogen atom or a C.sub.1 -C.sub.4 -alkyl group,R.sup.3 is a phenyl, pyridyl, pyrimidinyl or pyrazinyl group which is unsubstituted or mono- or disubstituted by halogen atoms, C.sub.1 -C.sub.4 -alkyl, trifluoromethyl, trifluoromethoxy, hydroxyl, C.sub.1 -C.sub.4 -alkoxy, amino, monomethylamino, dimethylamino, cyano or nitro groups and which may be fused to a benzene nucleus which may be unsubstituted or mono- or disubstituted by halogen atoms, C.sub.1 -C.sub.4 -alkyl, hydroxyl, trifluoromethyl, C.sub.1 -C.sub.4 -alkoxy, amino, cyano or nitro groups, and may contain 1 nitrogen atom, or to a 5- or 6-membered ring, which may contain 1-2 oxygen atoms,A is NH or an oxygen atom,Y is CH.sub.2, CH.sub.2 --CH.sub.2, CH.sub.2 --CH.sub.2 --CH.sub.2 or CH.sub.2 --CH,Z is a nitrogen atom, carbon atom or CH, it being possible for the linkage between Y and Z also to be a double bond,and n is 2, 3 or 4, and the physiologically tolerated salts thereof.
摘要翻译： PCT No.PCT / EP98 / 03230 Sec。 371 1999年12月6日第 102（e）日期1999年12月6日PCT提交1998年5月29日PCT公布。第WO98 / 56792号公报日期：19983年12月17日 - 取代的式I的3,4-二氢噻吩并[2,3-d]嘧啶衍生物，其中R 1和R 2是氢原子或C 1 -C 4 - 烷基，R 3是苯基，吡啶基， C 1 -C 4 - 烷基，三氟甲基，三氟甲氧基，羟基，C 1 -C 4 - 烷氧基，氨基，一甲基氨基，二甲基氨基，氰基或硝基被单取代或被二取代的嘧啶基或吡嗪基， C 1 -C 4烷基，羟基，三氟甲基，C 1 -C 4 - 烷氧基，氨基，氰基或硝基可被未被取代或单取代或被二取代的苯核，并且可以含有1个氮原子或5个 - 或6-元环，其可以含有1-2个氧原子，A是NH或氧原子，Y是CH 2，CH 2 -CH 2，CH 2 -CH 2 -CH 2或CH 2 -CH，Z是氮原子，碳原子或CH，Y和Z之间的连接也可以是双键，n是2,3或4，以及其生理上耐受的盐。

4. 发明授权

US06346622B1 2-substituted 1,2-benzisothiazole derivatives and their use as serotonin antagonists (5-HT1A, 5HT1B and 5-HT1D) 有权
标题翻译： 2-取代的1,2-苯并异噻唑衍生物及其用作5-羟色胺拮抗剂（5-HT1A，5HT1B和5-HT1D）
公开(公告)号：US06346622B1
公开(公告)日：2002-02-12
申请号：US09529828
申请日：2000-04-20
申请人： Wilfried Lubisch , Uta Dullweber , Dorothea Starck , Gerd Steiner , Alfred Bach , Franz Emling , Xavier Garcia-Ladona , Hans-Jürgen Teschendorf , Karsten Wicke
发明人： Wilfried Lubisch , Uta Dullweber , Dorothea Starck , Gerd Steiner , Alfred Bach , Franz Emling , Xavier Garcia-Ladona , Hans-Jürgen Teschendorf , Karsten Wicke
IPC分类号： A61K31425
CPC分类号： C07D275/06 , C07D417/04 , C07D417/06 , C07D417/12
摘要： where the substituents have the meanings indicated in the description, their preparation and use as serotonin antagonists.
摘要翻译：其中取代基具有说明书中所示的含义，其制备和用作血清素拮抗剂。

5. 发明授权

US06387912B1 Utilization of pyrimidine derivatives for preventing and treating cerebral ischaemia 失效
标题翻译：利用嘧啶衍生物预防和治疗脑缺血
公开(公告)号：US06387912B1
公开(公告)日：2002-05-14
申请号：US09889162
申请日：2001-07-11
申请人： Gerd Steiner , Kurt Schellhaas , Wilfried Lubisch , Uta Holzenkamp , Dorothea Starck , Monika Knopp , Laszlo Szabo , Franz Emling , Francisco Javier Garcia-Ladona , Hans-Peter Hofmann , Liliane Unger
发明人： Gerd Steiner , Kurt Schellhaas , Wilfried Lubisch , Uta Holzenkamp , Dorothea Starck , Monika Knopp , Laszlo Szabo , Franz Emling , Francisco Javier Garcia-Ladona , Hans-Peter Hofmann , Liliane Unger
IPC分类号： A61K31513
CPC分类号： A61K31/505
摘要： Use of pyrimidine derivatives of the formula I where the substituents are as defined in the description, and of their physiologically tolerated salts for producing medicaments for the prophylaxis and treatment of cerebral ischemia and strokes.
摘要翻译：使用式I的嘧啶衍生物，其中取代基如说明书中所定义，以及它们用于制备用于预防和治疗脑缺血和中风的药物的生理学耐受盐。

6. 发明授权

US06355647B1 3-substituted 3,4,5,7-tetrahedropyrrolo[3′,4′:4,5]thieno-[2,3-d]pyrimidine derivatives, their preparation and use 有权
标题翻译： 3-取代的3,4,5,7-四
取吡咯并[3'，4'：4,5]噻吩并[2,3-d]嘧啶衍生物，其制备和用途
公开(公告)号：US06355647B1
公开(公告)日：2002-03-12
申请号：US09485188
申请日：2000-02-07
申请人： Gerd Steiner , Uta Dullweber , Dorothea Starck , Alfred Bach , Karsten Wicke , Hans-Jürgen Teschendorf , Francisco-Javier Garcia-Ladona , Franz Emling
发明人： Gerd Steiner , Uta Dullweber , Dorothea Starck , Alfred Bach , Karsten Wicke , Hans-Jürgen Teschendorf , Francisco-Javier Garcia-Ladona , Franz Emling
IPC分类号： C07D49514
CPC分类号： C07D495/14
摘要： 3-Substituted 3,4,5,7-tetrahydropyrrolo[3′,4′:4,5]thieno-[2,3-d]pyrimidine derivatives of the formula I in which the substituents have the meanings stated in the description, their preparation and their use as drugs.
摘要翻译： 3-取代的式Iin的3,4,5,7-四氢吡咯并[3'，4'：4,5]噻吩并[2,3-d]嘧啶衍生物，其取代基具有如说明书中所述的含义，它们准备和用作药物。

7. 发明授权

US06414157B1 3-Substituted tetrahydropyridopyrimidinone derivatives, method for producing the same, and their use 有权
标题翻译： 3-取代的四氢吡啶并嘧啶酮衍生物，其制备方法及其用途
公开(公告)号：US06414157B1
公开(公告)日：2002-07-02
申请号：US09529231
申请日：2000-04-10
申请人： Wilfried Lubisch , Uta Dullweber , Dorothea Starck , Gerd Steiner , Alfred Bach , Franz Emling , Xavier Garcia-Ladona , Hans-Jürgen Teschendorf , Karsten Wicke
发明人： Wilfried Lubisch , Uta Dullweber , Dorothea Starck , Gerd Steiner , Alfred Bach , Franz Emling , Xavier Garcia-Ladona , Hans-Jürgen Teschendorf , Karsten Wicke
IPC分类号： C07D47100
CPC分类号： C07D471/04
摘要： 3-substituted tetrahydropyridopyrimidinone derivatives of the formula (I) wherein the radicals have the meanings given in the Description, to a method for producing said derivatives and, to their use for producing active ingredients for drugs.
摘要翻译：式（I）的3-取代四氢吡啶并嘧啶酮衍生物，其中基团具有说明书中给出的含义，所述衍生物的制备方法及其制备用于药物的活性成分的用途。

8. 发明授权

US06222034B1 3-substituted pyrido[4′,3′:4,5]thieno[2,3-d]pyrimidine derivatives, their preparation and their use 有权
标题翻译： 3-取代的吡啶并[4'，3'：4,5]噻吩并[2,3-d]嘧啶衍生物，其制备及其用途
公开(公告)号：US06222034B1
公开(公告)日：2001-04-24
申请号：US09254449
申请日：1999-03-10
申请人： Gerd Steiner , Wilfried Lubisch , Alfred Bach , Franz Emling , Karsten Wicke , Hans-Jürgen Teschendorf , Berthold Behl , Sharon Cheetham , Frank Kerrrigan
发明人： Gerd Steiner , Wilfried Lubisch , Alfred Bach , Franz Emling , Karsten Wicke , Hans-Jürgen Teschendorf , Berthold Behl , Sharon Cheetham , Frank Kerrrigan
IPC分类号： C07D49514
CPC分类号： C07D495/14
摘要： A 3-substituted 3,4,5,6,7,8-hexahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidine compound of formula I wherein R1 is hydrogen, C1-C4-alkyl, acetyl or benzoyl, optionally substituted phenyl-C1-C4-alkyl, naphthyl-C1-C3-alkyl, phenyl-C2-C3-alkanone or a phenylcarbamoyl-C2-alkyl, R2 is optionally substituted phenyl, pyridyl, pyrimidyl or pyrazinyl, or an optionally substituted bicyclus wherein one of the two fused rings is a phenyl, a pyridyl, a pyrimidyl or a pyrazinyl ring, A is NH or oxygen, B is hydrogen or methyl, C is hydrogen, methyl or hydroxyl, X is nitrogen, Y is CH2, CH2—C2, CH2—C2—CH2 or CH2—CH, Z is nitrogen, C or CH, and the linkage between Y and Z is a single or a double bond, and n is 2, 3 or 4, or a physiologically tolerated salt thereof, and compositions comprising them and their use as antagonists of 5HT1B and 5HT1A and for the treatment of depression and related disorders.
摘要翻译：式I的3-取代的3,4,5,6,7,8-六氢吡啶并[4'，3'：4,5]噻吩并[2,3-d]嘧啶化合物，其中R1为氢，C1-C4-烷基，乙酰基或苯甲酰基，任选取代的苯基-C 1 -C 4 - 烷基，萘基-C 1 -C 3 - 烷基，苯基-C 2 -C 3 - 烷酮或苯基氨基甲酰基-C 2 - 烷基，R 2是任选取代的苯基，吡啶基，嘧啶基或吡嗪基，或任选取代的双环，其中两个稠合环之一为苯基，吡啶基，嘧啶基或吡嗪基，A为NH或氧，B为氢或甲基，C为氢，甲基或羟基，X为氮，Y 是CH2，CH2-C2，CH2-C2-CH2或CH2-CH，Z是氮，C或CH，Y和Z之间的键是单键或双键，并且是2,3或4，或生理上耐受的盐，以及包含它们的组合物及其作为5HT1B和5HT1A的拮抗剂的用途以及用于治疗抑郁症和相关疾病的用途。

9. 发明授权

US6159981A 3-substituted pyrido [3',4':4,5] Thieno [2,3-d] pyrimidine derivatives, and production and use of the same 有权
标题翻译： 3-取代的吡啶并[3'，4'：4,5]噻吩并[2,3-d]嘧啶衍生物及其制备和使用
公开(公告)号：US6159981A
公开(公告)日：2000-12-12
申请号：US445178
申请日：1999-12-08
申请人： Gerd Steiner , Uta Dullweber , Dorothea Starck , Alfred Bach , Karsten Wicke , Hans-Jurgen Teschendorf , Francisco-Javier Garcia-Ladona , Franz Emling
发明人： Gerd Steiner , Uta Dullweber , Dorothea Starck , Alfred Bach , Karsten Wicke , Hans-Jurgen Teschendorf , Francisco-Javier Garcia-Ladona , Franz Emling
IPC分类号： A61K31/519 , A61P25/00 , A61P25/24 , A61P43/00 , C07D495/14 , A61K31/495 , A61K31/505
CPC分类号： C07D495/14
摘要： 3-Substituted 3,4,5,6,7,8-hexahydropyrido [3',4':4,5]-thieno[2,3-d]pyrimidine derivatives of the formula I ##STR1## where R.sup.1 is a hydrogen atom, a C.sub.1 -C.sub.4 -alkyl group, an acetyl group, a phenylalkyl C.sub.1 -C.sub.4 radical, the aromatic system being unsubstituted or substituted by halogen, C.sub.1 -C.sub.4 -alkyl, trifluoromethyl, hydroxyl, C.sub.1 -C.sub.4 -alkoxy, amino, cyano or nitro groups, or is a phenylalkanone radical, it being possible for the phenyl group to be substituted by halogen,R.sup.2 is a phenyl, pyridyl, pyrimidinyl or pyrazinyl group which is unsubstituted or mono- or disubstituted by halogen atoms, C.sub.1 -C.sub.4 -alkyl, trifluoromethyl, trifluoromethoxy, hydroxyl, C.sub.1 -C.sub.4 -alkoxy, amino, monomethylamino, dimethylamino, cyano or nitro groups and which may be fused to a benzene nucleus which can be unsubstituted or mono- or disubstituted by halogen atoms, C.sub.1 -C.sub.4 -alkyl, hydroxyl, trifluoromethyl, C.sub.1 -C.sub.4 -alkoxy, amino, cyano or nitro groups and may contain 1 nitrogen atom, or to a 5- or 6-membered ring which may contain 1-2 oxygen atoms,A is NH or an oxygen atom,Y is CH.sub.2, CH.sub.2 --CH.sub.2, CH.sub.2 --CH.sub.2 --CH.sub.2 or CH.sub.2 --CH,Z is a nitrogen atom, carbon atom or CH, it also being possible for the linkage between Y and Z to be a double bond,and n is 2, 3 or 4, and the physiologically tolerated salts thereof.
摘要翻译： PCT No.PCT / EP98 / 03231 Sec。 371 1999年12月8日第 102（e）日期1999年12月8日PCT提交1998年5月29日PCT公布。第WO98 / 56793号公报日期：19983年12月17日 - 取代式I的3,4,5,6,7,8-六氢吡啶并[3'，4'：4,5] - 噻吩并[2,3-d]嘧啶衍生物，其中R1是一个氢原子，一个C 1 -C 4烷基，一个乙酰基，一个苯基烷基C 1 -C 4基团，该芳族体系是未被取代的或被卤素，C 1 -C 4烷基，三氟甲基，羟基，C 1 -C 4烷氧基，氨基氰基或硝基，或者是苯基烷酮基，苯基可以被卤素取代，R2是苯基，吡啶基，嘧啶基或吡嗪基，其是未被取代的或被卤原子单取代或被C1- C4-烷基，三氟甲基，三氟甲氧基，羟基，C 1 -C 4 - 烷氧基，氨基，一甲基氨基，二甲基氨基，氰基或硝基，并且它们可以与苯核稠合，苯核可被未被取代或被卤素原子， C 4 - 烷基，羟基，三氟甲基，C 1 -C 4 - 烷氧基，氨基，氰基或硝基，并且可以含有1个氮原子，或可以含有5或6元环，含有1-2个氧原子，A是NH或氧原子，Y是CH 2，CH 2 -CH 2，CH 2 -CH 2 -CH 2或CH 2 -CH，Z是氮原子，碳原子或CH，也可以是 Y与Z之间的连接为双键，n为2,3或4，以及其生理上耐受的盐。

10. 发明申请

US20070066627A1 Hydrazone derivatives for combatting harmful insects and arachnids 审中-公开
标题翻译：腙类衍生物用于防治有害昆虫和蜘蛛
公开(公告)号：US20070066627A1
公开(公告)日：2007-03-22
申请号：US10557881
申请日：2004-05-26
申请人： Michael Hofmann , Markus Kordes , Udo Lange , Ernst Baumann , Wolfgang von Deyn , Michael Puhl , Thomas Schmidt , Gerd Steiner , Michael Treacy , Deborah Culbertson , Toni Bucci , Hong-Ming Shieh , Lester Maravetz
发明人： Michael Hofmann , Markus Kordes , Udo Lange , Ernst Baumann , Wolfgang von Deyn , Michael Puhl , Thomas Schmidt , Gerd Steiner , Michael Treacy , Deborah Culbertson , Toni Bucci , Hong-Ming Shieh , Lester Maravetz
IPC分类号： A01N43/82 , A01N43/78 , A01N43/56 , A01N43/06 , A01N43/40 , A01N43/08 , A01N43/80 , A01N43/50
CPC分类号： A01N43/80 , A01N37/28 , A01N43/08 , A01N43/10 , A01N43/12 , A01N43/38 , A01N43/40 , A01N43/50 , A01N43/56 , A01N43/78 , A01N51/00
摘要： The present invention relates to a method for combating insects or arachnids which comprises contacting the insects or the arachnids, their habitat, breeding ground, food supply, plant, seed, soil, area, material or environment in which the insects or the arachnids are growing or may grow, or the materials, plants, seeds, soils, surfaces or spaces to be protected from insect or arachnid attack or infestation with a pesticidally effective amount of a compound of the general formula (I) or a salt thereof wherein: Ar is a cyclic radical, n is 0 or 1, X is CO or SO2 and R1 to R4 are as defined in claim 1.
摘要翻译：本发明涉及一种防治昆虫或蛛形纲的方法，包括使昆虫或蜘蛛，其栖息地，繁殖地，食物供应，植物，种子，土壤，区域，材料或昆虫或蜘蛛生长环境接触或可能生长的材料，植物，种子，土壤，表面或空间，以防止昆虫或蛛形纲虫攻击或侵染与杀虫有效量的通式（I）化合物或其盐，其中：Ar是环状基团，n为0或1，X为CO或SO 2，R 1至R 4如权利要求1所定义。

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