公开(公告)号：JP2000080089A

公开(公告)日：2000-03-21

申请号：JP18237199

申请日：1999-06-28

Applicant: BASF AG

Inventor： WAGNER OLIVER ,  ROEHL FRANZ ,  GROSSMANN KLAUS ,  RALF-MICHAEL SCHMIDT ,  SONNEWALD UWE ,  HAJIREZAEI MOHAMMAD DR

IPC: A01N43/78 ,  C07D277/82

Abstract: PROBLEM TO BE SOLVED: To obtain a new ferredoxin: NADP reductase inhibitor expressed by a specific chemical structural formula, capable of being used by mixing with a noxious insecticide, a bactericide for plant pathogenic bacteria or the like, and useful as a herbicide, etc. SOLUTION: This ferredoxin: NADP reductase inhibitor is a compound of formula I [formula II expresses E/Z isomers; Y is CO or SO2; R1 to R3 are each H, a halogen, a 1-6C (halo)alkyl, a 1-6C (halo)alkoxy, a 1-6C alkoxyalkyl, a 1-6C alkylthio or the like; R4 is H or a 1-6C alkyl; R5 to R7 are each H, a halogen, cyano, a 1-30C alkyl, a 1-30C alkoxyalkyl, a 1-10C alkylthio, SO3H or the like]. Further, the compound of formula I is obtained e.g. by reacting a compound of formula III with a compound of formula IV in an inert organic solvent in the presence of a base such as triethylamine.

公开(公告)号：WO2006122740A3

公开(公告)日：2007-02-22

申请号：PCT/EP2006004573

申请日：2006-05-15

Applicant: BASF AG ,  WAGNER OLIVER

Inventor： WAGNER OLIVER

IPC: C07D487/04 ,  A01N43/90

CPC classification number: C07D487/04 ,  A01N43/90

Abstract: The invention relates to novel 7-amino-6-hetarylimidazolo[1,2-a]pyrimidine compounds of formula (I), the salts thereof, the use of said compounds for controlling harmful fungi, and agricultural pesticides containing at least one such compound as an active component. The substituents Het, X, Y 1 , and Y 2 in formula (I) have the following meanings: Het represents a five-membered or six-membered heteroaromatic radical which can contain one, two, three, or four heteroatoms selected among O, S, and N as ring members, said five-membered or six-membered heteroaromatic radical being optionally provided with one, two, three, or four identical or different substituents L; X represents hydrogen, OH, halogen, cyano, NR 3 R 4 , C 1 -C 8 alkyl, C 1 -C 8 alkoxy, C 1 -C 8 alkylthio, C 1 -C 8 alkylsulfinyl, C 1 -C 8 alkylsulfonyl, C 2 -C 8 alkenyl, or C 2 -C 8 alkinyl, the seven latter radicals being optionally halogenated in full or in part and/or optionally carrying one, two, or three substituents selected among nitro, cyano, C 1 -C 2 alkoxy, C 1 -C 4 alkoxycarbonyl, amino, C 1 -C 4 alkylamino, and di-C 1 -C 4 alkylamino. R 3 and R 4 independently have the meanings indicated for R 1 or R 2 ; Y 1 , Y 2 independently represent hydrogen, halogen, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkyl halide, C 3 -C 7 cycloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, or C 1 -C 4 haloalkoxy; and R 1 , R 2 have the meanings indicated in the claims and the description.

Abstract translation: 本发明涉及新颖的7-氨基-6- hetarylimidazolo [1,2-A]下式的嘧啶化合物，其包含至少一种这样的化合物作为有效成分的I和其盐以及在防治有害真菌中使用这些化合物中，和植物保护剂 ， 在式I中，取代基的Het，X，Y ^{1 和Y 2 具有以下含义：的Het：含有5-或6-元杂芳基1，2 ，3或4个可以是O，S和N的已选择的杂原子作为环成员，其中所述5元或6元杂芳族残基1，2，3或4个相同或不同的取代基L可以包括，X：氢，OH，卤素， 氰基，NR 3 - [R 4 ，C _{1 -C 8 烷基，C 1 -C 8 烷氧基，C 1 -C 8 烷硫基，C 1 -C 8 烷基亚磺酰基，C 1 -C 8 烷基磺酰基，C 2 -C 8 链烯基或C 2 -C 8 炔基，其中所述7最后提到的基团可以部分或完全卤化和/或一个，两个或三个选自硝基取代基取代， 氰基，C 1 -C 2 烷氧基，C 1 -C 4 烷氧基羰基，氨基，C < SUB> 1 -C 4 -A lkylamino和二C 1 -C 4可以烷基氨基磨损，且其中R 3 和R 4 独立地 从对方， 2 具有对于R所给出的含义 1 或R; ÿ 1 ，Y 2 彼此独立地为氢，卤素，氰基，C 1 -C 4 烷基， ç 1 -C 4 卤代烷基，C 3 -C 7 环烷基，C 1 < / SUB> -C 4 烷氧基，C 1 -C 4 烷硫基，C 1 -C < SUB> 4 烷基亚磺酰基，C 1 -C 4 烷基磺酰基或C 1 -C 4 卤代烷氧基; [R 1 ，R 2 具有权利要求书和说明书中给出的含义。}}

公开(公告)号：WO2005087770A3

公开(公告)日：2005-12-08

申请号：PCT/EP2005002424

申请日：2005-03-08

Applicant: BASF AG ,  TORMO I BLASCO JORDI ,  BLETTNER CARSTEN ,  MUELLER BERND ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NIEDENBRUECK MATTHIAS ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD ,  HUENGER UDO

Inventor： TORMO I BLASCO JORDI ,  BLETTNER CARSTEN ,  MUELLER BERND ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NIEDENBRUECK MATTHIAS ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD ,  HUENGER UDO

IPC: C07D487/04

CPC classification number: C07D487/04

Abstract: The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R represents alkyl, alkoxyalkyl, alkenyl or alkynyl; R represents alkyl, alkoxyalkyl, alkenyl or alkynyl, R and/or R being substituted according to the description. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.

Abstract translation: 5,6-二烷基 - 7-氨基三唑并嘧啶，其中取代基具有式（I）的以下含义：R t <1>是烷基，烷氧基烷基，烯基或炔基; [R <2>是烷基，烷氧基烷基，烯基或炔基; 其中R <1>和/或R <2>取代根据描述; 一种用于制备这些化合物，含有它们和它们在防治植物病原性有害真菌的用途的组合物的过程。

公开(公告)号：WO2005095404A3

公开(公告)日：2006-04-06

申请号：PCT/EP2005003208

申请日：2005-03-26

Applicant: BASF AG ,  BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  RACK MICHAEL ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

Inventor： BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  RACK MICHAEL ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

IPC: C07D487/04 ,  A01N43/90

CPC classification number: A01N43/90 ,  C07D487/04

Abstract: The invention relates to the 6-(2-fluorophenyl)-triazolopyrimidines of formula (I), wherein the substituents are defined as follows: R

Abstract translation: 本申请公开了式-6-（2-氟苯基） - 三唑并嘧啶予其中的取代基具有下列含义：R t

公开(公告)号：WO2005095405A3

公开(公告)日：2005-12-22

申请号：PCT/EP2005004187

申请日：2005-03-29

Applicant: BASF AG ,  BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  RACK MICHAEL ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

Inventor： BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  RACK MICHAEL ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

IPC: A01N43/90 ,  C07D487/04

CPC classification number: A01N43/90 ,  C07D487/04

Abstract: The invention relates to 6-(2,6-dichlorophenyl)-triazolopyrimidines of formula (I) wherein the substituents have the following designations: R and R represent hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, halogencycloalkenyl, alkinyl, halogenalkinyl or phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group containing O, N or S; R and R can also form, together with the nitrogen atom to which they are bound, a five-membered or six-membered heterocycle or heteroaryl which is bound by N and contains between one and three other heteroatoms from the group containing O, N and S as a cyclic member and is substituted according to the description; and X represents alkyl, cyano, alkoxy, halogenalkoxy, alkenyloxy or halogenalkenyloxy, but does not represent C1-C4 alkyl when R and R together represent piperidin-1-yl or 4-methylpiperidin-1-yl. The invention also relates to a method for producing said compounds, agents containing the same, and the use thereof for controlling plant pathogenic fungi.

Abstract translation: 6-（2,6-二氯苯基） - 三唑并嘧啶的式（I）的其中取代基具有以下含义：R t <1>，R <2>是氢，烷基，卤代烷基，环烷基，卤代环烷基，烯基，卤代烯基，环烯基，卤代环烯基 基，炔基，卤代炔基，或苯基，萘基，或含有选自O，N，或S，R <1>和R <2>也可以，一起一至四个杂原子的五元或六元饱和，部分不饱和或芳族杂环 形成一个五元或六元杂环基或杂芳基的氮原子与它们所连接，这是经N个附接和选自O，N和S的一至三个另外的杂原子作为环成员，并且可以根据该描述被取代; X为烷基，氰基，烷氧基，卤代烷氧基，烯氧基或卤代链烯氧基，其中X不为C1-C4烷基，当R <1>和R <2>是常见的哌啶-1-基或4-甲基 - 哌啶-1-基; 一种用于制备这些化合物，含有它们和它们在防治植物病原性有害真菌的用途的组合物的过程。

公开(公告)号：WO2005110080A2

公开(公告)日：2005-11-24

申请号：PCT/EP2005005070

申请日：2005-05-11

Applicant: BASF AG ,  BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

Inventor： BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

IPC: A01N20060101 ,  A01N43/90 ,  A01N

CPC classification number: A01N43/90 ,  A01N59/06 ,  A01N59/02 ,  A01N57/12 ,  A01N47/38 ,  A01N47/34 ,  A01N47/24 ,  A01N47/04 ,  A01N43/50 ,  A01N43/76 ,  A01N43/653 ,  A01N43/36 ,  A01N43/40 ,  A01N43/32 ,  A01N37/48 ,  A01N37/46 ,  A01N37/38 ,  A01N37/34 ,  A01N2300/00

Abstract: The invention relates to fungicidal mixtures containing in the form of active components 1) 5-methyl-7-amino-triazolopyrimidine of formula (I), wherein R is alkyl, halogenalkyl, alkenyl or cyclopentyl, R is hydrogen or alkyl, R and R together with the nitrogen atom to which they are bound may form a piperidinyl cycle substitutable by a methyl group, L is fluorine or chlorine, L , L are independently from each other hydrogen, fluorine or chlorine and 2) at least one type of active substance selected from groups A) azoles, B) strobilurins, C) acyl alanines, D) amine derivatives, E) anilinopyrimidines; F) dicarboximides; G) cinnamic acid amides and analogues thereof, H) antibiotics, K) dithiocarbamates, L) heterocyclic compounds, M) sulphur and copper fungicides, N) nitrophenyl derivatives, O) phenylpyrroles, P) sulfenic acid derivatives, Q) other fungicides and R) growth retardants according to the descriptions, wherein said mixtures contain the compounds in a synergically efficient amount. Novel triazolopyrimidines, methods for controlling pathogenic fungi using the mixtures of the compound (I) with active substances of the groups A) and R), the use the compounds (I) with the active substances of the groups A) and R) for producing said mixtures and agents containing said mixtures are also disclosed.

Abstract translation: 一种杀真菌混合物，其包含作为活性组分：1）式（I）的5-甲基-7-氨基三唑并嘧啶，其中R <1>是烷基，卤代烷基，链烯基或环戊基; [R <2>是氢或烷基; [R <1>和R <2>也可以与氮原子一起与它们所连接的形式，其可以由甲基取代的哌啶环; →<1>是氟或氯; →<2>，L <3>独立地是氢，氟或氯; 和2）选自组A）唑类中的至少一种活性化合物; B）嗜球果伞素; C）酰基丙氨酸类; D）胺衍生物; E）苯胺基嘧啶; F）二甲酰亚胺; G）肉桂酸和类似物; 1H）抗生素; K）二硫代氨基甲酸酯; L）杂环化合物; M）硫和铜杀真菌剂; N）硝基苯基衍生物; O）苯基吡咯; P）Sulfensäurederivate; Q）其他杀菌剂; R）Wachstumsretardantien; 根据描述; 在协同有效量; 新的三唑并嘧啶，用于控制使用I化合物的混合物与基团A），以R的活性成分）包含这些混合物的有害真菌及其制造这样的混合物使用I化合物与基团A）至R）的活性成分和组合物的方法 ，

公开(公告)号：WO2005087771A3

公开(公告)日：2005-12-01

申请号：PCT/EP2005002425

申请日：2005-03-08

Applicant: BASF AG ,  TORMO I BLASCO JORDI ,  BLETTNER CARSTEN ,  MUELLER BERND ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NIEDENBRUECK MATTHIAS ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

Inventor： TORMO I BLASCO JORDI ,  BLETTNER CARSTEN ,  MUELLER BERND ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  RHEINHEIMER JOACHIM ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NIEDENBRUECK MATTHIAS ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

IPC: C07D487/04

CPC classification number: C07D487/04

Abstract: The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R represents alkyl or alkoxyalkyl; R represents alkyl, R and/or R being substituted according to the description. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.

Abstract translation: 式（I）的5,6-二烷基 - 7-氨基 - 三唑并嘧啶，其中取代基具有以下含义：R t <1>是烷基或烷氧基烷基，R <2>是烷基，其中R <1>和/或R <2> 可以如上所述被替换; 这些化合物的制备方法，含有它们的试剂及其用于防治植物病原性有害真菌的用途。

公开(公告)号：WO2005080396A2

公开(公告)日：2005-09-01

申请号：PCT/EP2005001965

申请日：2005-02-24

Applicant: BASF AG ,  SCHWOEGLER ANJA ,  GEWEHR MARKUS ,  MUELLER BERND ,  GROTE THOMAS ,  GRAMMENOS WASSILIOS ,  TORMO I BLASCO JORDI ,  RHEINHEIMER JOACHIM ,  BLETTNER CARSTEN ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  WAGNER OLIVER ,  STIERL REINHARD ,  SCHOEFL ULRICH ,  STRATHMANN SIEGFRIED ,  SCHERER MARIA

Inventor： SCHWOEGLER ANJA ,  GEWEHR MARKUS ,  MUELLER BERND ,  GROTE THOMAS ,  GRAMMENOS WASSILIOS ,  TORMO I BLASCO JORDI ,  RHEINHEIMER JOACHIM ,  BLETTNER CARSTEN ,  SCHAEFER PETER ,  SCHIEWECK FRANK ,  WAGNER OLIVER ,  STIERL REINHARD ,  SCHOEFL ULRICH ,  STRATHMANN SIEGFRIED ,  SCHERER MARIA

IPC: A01N43/90 ,  C07D487/04 ,  C07D487/00

CPC classification number: C07D487/04

Abstract: The invention relates to azolopyrimidine compounds of general formula (I), wherein A represents N or C-R ; X and Y, independent of one another, represent a chemical compound or oxygen, sulphur or a group N-R ; the variables R , R , R , R , R , R and R have the meanings cited in the claims and the description. The invention also relates to tautomers of compounds of formula (I) and to the agriculturally compatible salts of compounds (I) and of the tautomers thereof. The invention further relates to the use of azolopyrimidine compounds of general formula (I), to the tautomers thereof and to the agriculturally compatible salts thereof which are used to combat phytopathogenic fungi, and to a method for combating phytopathogenic fungi and means for combating fungi, said means containing at least one compound of general formula (I), a tautomer of formula (I) and/or an agriculturally compatible salt thereof or the tautomer thereof and at least one liquid or solid carrier medium.

Abstract translation: 本发明涉及通式（I）的唑基嘧啶化合物，其中A是N或C-R 6; X，Y彼此独立地代表化学键或氧，硫或基团N-R 7; 其中变量R <1>，R <2>，R <3>，R <4>，R <5> - [R <6>和R <7>具有权利要求书所给出的含义和描述中，互变异构体 式（I）化合物和化合物I及其互变异构体的农业上可接受的盐。 本发明还涉及使用通式（I）的唑并嘧啶化合物，它们的互变异构体以及它们用于防治植物致病真菌（=有害真菌），以及用于防治植物病原性有害真菌的方法和用于防治有害真菌的手段农业上可接受的盐，含 至少一种通式（I）的化合物，（I）的互变异构体和/或其农业上可接受的盐或其互变异构体以及至少一种液体或固体载体。

公开(公告)号：WO03090539A8

公开(公告)日：2004-12-16

申请号：PCT/EP0304136

申请日：2003-04-22

Applicant: BASF AG ,  WAGNER OLIVER ,  RACK MICHAEL ,  WITSCHEL MATTHIAS ,  ZAGAR CYRILL ,  LANDES ANDREAS

Inventor： WAGNER OLIVER ,  RACK MICHAEL ,  WITSCHEL MATTHIAS ,  ZAGAR CYRILL ,  LANDES ANDREAS

IPC: A01N43/80 ,  C07D261/08 ,  C07D413/04 ,  C07D413/14 ,  C07D417/04

CPC classification number: C07D413/04 ,  A01N43/80 ,  C07D261/08 ,  C07D413/14 ,  C07D417/04

Abstract: The invention relates to 3-heteroaryl substituted isoxazolines of formula (I), or to their salts that can be used for agricultural purposes. In said formula, the variables are defined as follows: X represents a substituted 5-membered heteroaryl comprising between one and four nitrogen atoms, or between one and three nitrogen atoms and one oxygen or sulphur atom, or one oxygen or sulphur atom, or represents a substituted 6-membered heteroaryl comprising between one and four nitrogen atoms, whereby the aforementioned 5-membered heteroaryl is not pyrazolyl or thienyl; R - R represent hydrogen, alkyl or haloalkyl; Y represents an optionally substituted aryl, or benzo[1,4]dioxonyl, benzo[1,3]dioxolanyl, 2,3-dihydrobenzofuranyl or benzimidazole, or an optionally substituted 5- to 6-membered heteroaryl. The invention also relates to methods and intermediate products for the production of said compounds, in addition to the use thereof or of agents containing the compounds for controlling undesired plants.

Abstract translation: 本发明涉及式（I）的3- heteroarylsubstituerte异恶唑啉：其中各变量具有以下含义：X为取代的具有一至四个氮原子或具有一至三个氮原子和一个氧或硫原子，或具有5元杂芳基 一个氧或硫原子; 的或取代的具有一至四个氮原子的6元杂芳基; 其中，上述的5元杂芳基未被吡唑基或噻吩基; [R <1> - R的<7>是氢，烷基或卤代烷基; Y是任选取代的芳基，或苯并[1,4] dioxonyl，苯并[1,3]二氧戊环基，2,3-二氢苯并呋喃基或苯并咪唑; 或任选取代的5-至6-元杂芳基; 及其可农用盐，它们的制备方法和中间体; 和使用这些化合物或包含用于控制不希望的植物的装置这些化合物。

公开(公告)号：WO9957111A9

公开(公告)日：2001-03-01

申请号：PCT/EP9902703

申请日：1999-04-22

Applicant: BASF AG ,  WITSCHEL MATTHIAS ,  LANGEMANN KLAUS ,  DEYN WOLFGANG VON ,  MISSLITZ ULF ,  BAUMANN ERNST ,  ENGEL STEFAN ,  MAYER GUIDO ,  NEIDLEIN ULF ,  WAGNER OLIVER ,  GOETZ ROLAND ,  OTTEN MARTINA ,  WESTPHALEN KARL OTTO ,  WALTER HELMUT

Inventor： WITSCHEL MATTHIAS ,  LANGEMANN KLAUS ,  VON DEYN WOLFGANG ,  MISSLITZ ULF ,  BAUMANN ERNST ,  ENGEL STEFAN ,  MAYER GUIDO ,  NEIDLEIN ULF ,  WAGNER OLIVER ,  GOETZ ROLAND ,  OTTEN MARTINA ,  WESTPHALEN KARL-OTTO ,  WALTER HELMUT

IPC: A01N43/08 ,  A01N43/18 ,  A01N43/32 ,  A01N43/36 ,  A01N43/54 ,  A01N43/56 ,  A01N43/653 ,  A01N43/80 ,  A01N43/84 ,  C07D335/06 ,  C07D339/08 ,  C07D409/06 ,  C07D409/08 ,  C07D413/06 ,  C07D413/08

CPC classification number: C07D335/06 ,  A01N43/08 ,  A01N43/18 ,  A01N43/36 ,  A01N43/54 ,  A01N43/56 ,  A01N43/653 ,  A01N43/80 ,  A01N43/84 ,  C07D339/08 ,  C07D409/08

Abstract: The invention relates to cyclohexenondioxothiochromanoyl derivatives of formula (I) wherein the variables have the following meanings: X is oxygen, sulphur, S=O, S(=O)2, CR R , C=O or C=NR ; R is hydrogen, nitro, halogen, cyano, alkyl, alkyl halide, alkoxy, halogenalkoxy, alkylthio, halogenalkylthio, alkylsulfinyl, halogenalkylsulfinyl, alkylsulfonyl, halogenalkylsulfonyl, optionally substituted aminosulfonyl or optionally substituted sulfonylamino; R is alkyl, alkyl halide, alkoxy or halogenalkoxy; R is hydrogen, alkyl or halogen; and R , R are hydrogen, nitro, halogen, cyano, alkyl, alkyl halide, alkoxy, halogenalkoxy, alkylthio, halogenalkylthio, alkylsulfinyl, halogenalkylsulfinyl, alkylsulfonyl, halogenalkylsulfonyl or substituted amino; or R and R together form a chain which can be substituted and/or interrupted by oxygen or sulphur; or an optionally substituted methylide group; l is 0 to 4; R is substituted (3-oxo-1-cyclohexen-2-yl)-carbonyl or substituted (1,3-dioxo-2-cyclohexyl-methylides. The invention also relates to the agriculturally usable salts of said derivatives, to methods for producing the derivatives, to substances containing them, and to the use of the derivatives or substances containing them for combating undesirable plants.

Abstract translation: 式（I），其中各变量具有以下含义的Cyclohexenondioxothiochromanoyl衍生物：X是氧，硫，S = O，S（= O）2，CR <4> - [R <5>，C = O或C = NR < 6>; [R <1>是氢，硝基，卤素，氰基，烷基，卤代烷基，烷氧基，卤代烷氧基，烷硫基，卤代烷硫基，烷基亚磺酰基，卤代烷，烷基磺酰基，卤代烷基磺酰基，任选子氨基磺酰基，磺酰氨基或可能子..; [R <2>是烷基，卤代烷基，烷氧基或卤代烷氧基; [R <3>是氢，烷基或卤素; [R <4>，R <5>为氢，硝基，卤素，氰基，烷基，卤代烷基，烷氧基，卤代烷氧基，烷硫基，卤代烷硫基，烷基亚磺酰基，卤代烷，烷基磺酰基，卤代烷基磺酰基或亚氨基。 或R <4>和R <5>一起形成取代和/或可以被氧或硫中断的链条; 或任选取代的亚甲基团的; 1 0至4; [R <7>取代的（3-氧代-1-环己烯-2-基） - 羰基，或取代的（1,3-二氧代-2-环己基）亚甲基; 及其可农用盐; 一种用于Cyclohexenondioxothiochromanoyl衍生物的制备方法; 含有它们并使用这些衍生物或包含它们用于控制不希望的植物的组合物的组合物。