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    • 1. 发明申请
    • PESTICIDAL ACTIVE MIXTURES COMPRISING AMINOTHIAZOLINE COMPOUNDS
    • 包含氨基苯甲酸化合物的农药活性混合物
    • WO2009118297A2
    • 2009-10-01
    • PCT/EP2009/053402
    • 2009-03-24
    • BASF SEKORDES, MarkusVEZOUET, Ronan LeLANGEWALD, JürgenPAULINI, RalphCULBERTSON, Deborah L.ANSPAUGH, Douglas D.JOSE, Luiz AntonioOLOUMI-SADEGHI, Hassan
    • KORDES, MarkusVEZOUET, Ronan LeLANGEWALD, JürgenPAULINI, RalphCULBERTSON, Deborah L.ANSPAUGH, Douglas D.JOSE, Luiz AntonioOLOUMI-SADEGHI, Hassan
    • A01N43/78A01P5/00A01P7/02A01P7/04
    • A01N43/78A01N43/08A01N43/40A01N43/54A01N43/56A01N43/58A01N43/707A01N43/88A01N43/90A01N47/02A01N47/06A01N47/30A01N47/34A01N47/40A01N51/00A01N53/00A01N2300/00
    • The present invention relates to pesticidal mixtures comprising as active compounds 1 ) at least one aminothiazoline compound (I) of formula (I), tautomer a), b) wherein R 1 is selected from hydrogen, COCH 3 , COCH 2 CH 3 or COCH 2 C(CH 3 ) 3 ; R 2 and R 3 together with the carbon atoms of the phenyl ring to which they are attached form a ring which, depending on the tautomeric formula I a) or b) is depicted as: a benzene ring, a saturated 5-, 6-, or 7-membered carbocycle, a partially unsaturated 5-, 6-, or 7-membered carbocycle, a 5-, 6-, or 7-membered saturated heterocycle, a partially unsaturated 5-, 6-, or 7-membered heterocycle, which heterocycles contain 1, 2, or 3 heteroatoms selected from O, S and N as ring members, and a 5- or 6- membered heteroaromatic ring which contains 1, 2, or 3 heteroatoms selected from O, S and N as ring members, and wherein the ring is unsubstituted or may carry any combination of 1, 2, 3, or 4 radicals selected from the group consisting of halogen, CH 3 , CH 2 CH 3 , CF 3 , CH 3 O, cyano and (=0) (oxo); R 4 is selected from hydrogen, fluoro, chloro, bromo, CF 3 , CH 3 O or CH 3 ; R 5 , R 6 are selected from hydrogen, chloro, fluoro, bromo, CH 3 , CH 3 O or CF 3 , wherein at least one of R 5 or R 6 is not hydrogen; with the proviso that R 2 and R 3 together do not form a -OCH 2 -O- or a -OCF 2 O-group; or the tautomers, enantiomers, diastereomers or salts thereof, and 2) at least one active compound Il selected from group A as defined in the description, use of these mixtures for combating insects, acarids, or nematodes, and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites using these mixtures.
    • 本发明涉及包含作为活性化合物的至少一种式(I)的至少一种氨基噻唑啉化合物(I),互变异构体a),b)其中R 1选自氢,COCH 3,COCH 2 CH 3或COCH 2 C(CH 3)3的农药混合物; R2和R3与它们所连接的苯环的碳原子一起形成环,其取决于互变异构体式a a)或b)被描述为:苯环,饱和的5-,6-或 7元碳环,部分不饱和5-,6-或7-元碳环,5-,6-或7-元饱和杂环,部分不饱和5-,6-或7-元杂环,其中 杂环含有选自O,S和N作为环成员的1,2或3个杂原子,以及含有1,2或3个选自O,S和N作为环成员的杂原子的5-或6-元杂芳族环, 并且其中所述环是未取代的或可以携带选自卤素,CH 3,CH 2 CH 3,CF 3,CH 3 O,氰基和(= O)(氧代)的1,2,3或4个基团的任何组合。 R4选自氢,氟,氯,溴,CF 3,CH 3 O或CH 3; R5,R6选自氢,氯,氟,溴,CH3,CH3O或CF3,其中R5或R6中的至少一个不是氢; 条件是R2和R3一起不形成-OCH2-O-或-OCF2O-基团; 或其互变异构体,对映异构体,非对映异构体或其盐,以及2)选自如说明书中定义的组A的至少一种活性化合物II,这些混合物用于防治昆虫,螨虫或线虫的用途,以及治疗,控制 ,防止或保护动物免受使用这些混合物的寄生虫的感染或感染。
    • 2. 发明申请
    • RESORCINE DERIVATIVES AND THEIR USE AS PESTICIDES
    • WO2007054558A3
    • 2007-05-18
    • PCT/EP2006/068329
    • 2006-11-10
    • BASF AKTIENGESELLSCHAFTPUHL, MichaelKORDES, MarkusPOHLMAN, MatthiasGÖTZ, NorbertRACK, MichaelLANGEWALD, JürgenSCHNEIDER, FelixANSPAUGH, Douglas D.CULBERTSON, Deborah L.OLOUMI-SADEGHI, HassanKUHN, David G.
    • PUHL, MichaelKORDES, MarkusPOHLMAN, MatthiasGÖTZ, NorbertRACK, MichaelLANGEWALD, JürgenSCHNEIDER, FelixANSPAUGH, Douglas D.CULBERTSON, Deborah L.OLOUMI-SADEGHI, HassanKUHN, David G.
    • C07C43/29C07D213/16C07D213/26C07D277/22A01N29/10
    • This invention relates to resorcine derivatives of formula (I) wherein R 1 is phenyl or a 5- to 6-membered heteroaromatic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl or the heteroaromatic ring may be fused to a ring selected from phenyl and a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl or the 5- to 6-membered heteroaromatic ring or the respective fused ring systems may be unsubstituted or substituted by any combination of 1 to 6 optionally substituted groups R 3 , wherein R 3 is halogen, cyano, nitro, hydroxy, mercapto, amino, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, haloalkyl, haloalkenyl, haloalkynyl, halocycloalkyl, halocycloalkenyl, alkoxy, alkenyloxy, alkynyloxy, haloalkoxy, haloalkenyloxy, haloalkynyloxy, alkylthio, alkenylthio, alkynylthio, haloalkylthio, haloalkenylthio, haloalkynylthio, alkylamino, alkenylamino, alkynylamino, dialkylamino, dialkenylamino, dialkynylamino, alkyl-alkenylamino, alkyl-alkynylamino, alkenyl- alkynylamino, trialkylsilyl, or phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which phenyl and which heteroaromatic ring may be bonded via an oxygen or a sulfur atom, or -C(=G)R a , -C(=G)OR a , -C(=G)NR a 2 , -C(=G)[N=SR a 2 ], -C(=NOR a )R a , -C(=NOR a )NR a 2 , -C(=NNR a 2 )R a , -OC(=G)-OC(=G)OR a , N=SR a 2 , -NR a C(=G)R a , -N[C(=G)R a ] 2 , - NR a C(=G)OR a , -C(=G)NR a -NR a 2 , -C(=G)NR a -NR a [C(=G)R a ], -NR a -C(=G)NR a 2 , -NR a -NR a C(=G)R a , -NR a -N[C(=G)R a ] 2 , -N[(C=G)R a ]-NR a 2 , -NR a -NR a [(C=G)GR a ], -NR a [(C=G)NR a 2 , -NR a [C=NR a ]R a , -NR a (C=NR a )NR a 2 , -O-NR a 2 , -O-NR a (C=G)R a , - SO 2 NR a 2 , -NR a SO 2 R a , -S(=O)R a , -S(=O) 2 R a , -SO 2 OR a , or -OSO 2 R a , wherein G is oxygen or sulfur and Ra is as defined in the description, R 2 is hydrogen, halogen, cyano, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkoxy, or haloalkoxy, x is 2, 3, 4, 5, 6, or 7, or the diastereomers, enantiomers, salts or N-oxides thereof, with the proviso that R 1 is not 5-chloro-2,2,-dimethyl-2,3-dihydrobenzo[b]furan-7-yl when R 2 is hydrogen and x is 3 or 4, processes and intermediates for the preparation of compounds I, use of compounds I for combating insects, acarids, or nematodes, and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites using compounds I.
    • 10. 发明申请
    • DICYANO ALKANOIC ACID AMIDES FOR COMBATING ANIMAL PESTS
    • DICYANO ALKANOIC ACIDES用于组合动物乳制品
    • WO2007014899A1
    • 2007-02-08
    • PCT/EP2006/064728
    • 2006-07-27
    • BASF AKTIENGESELLSCHAFTHOFMANN, MichaelBASTIAANS, Henricus, Maria, MartinusLANGEWALD, JürgenOLOUMI-SADEGHI, HassanCULBERTSON, Deborah, L.
    • HOFMANN, MichaelBASTIAANS, Henricus, Maria, MartinusLANGEWALD, JürgenOLOUMI-SADEGHI, HassanCULBERTSON, Deborah, L.
    • A01N37/34C07C255/19C07C253/30
    • A01N37/34C07C255/19C07C255/20C07C255/21C07C317/44
    • Dicyano alkanoic acid amides of formula (I), wherein R 1 is H, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, or haloalkynyl; R 2 is H, CN, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkyl, halocycloalkyl, alkoxy, or haloalkoxy; R 3 and R 4 are H, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkyl, halocycloalkyl, cycloalkenyl, halocycloalkenyl, or R 3 and R 4 together can be alkylene, haloalkylene, alkenylene or haloalkenylene; X is O or S; R 5 and R 6 are H, alkyl, optionally substituted with 1 to 3 groups CN, NO 2 , OH, NR 7 R 8 , alkoxy, haloalkoxy, alkylthio, haloalkylthio, cycloalkyl, halocycloalkyl and optionally substituted phenyl; or haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, NR 7 R 8 , alkoxycarbonyl, haloalkoxycarbonyl, alkenyloxycarbonyl, haloalkenyloxycarbonyl, alkylcarbonyl, haloalkylcarbonyl, R 7 R 8 N-C(=O)-, phenylcarbonyl, benzylcarbonyl or phenyl wherein phenylcarbonyl, benzylcarbonyl and phenyl are optionally substituted; or R 5 and R 6 are a saturated, partially unsaturated or unsaturated 5- to 6-membered heterocyclic radical which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur and which radical may be bonded via a carbonyl (C(=O)) linkage, and which radical is optionally substituted; R 7 , R 8 are H, alkyl, haloalkyl, alkylcarbonyl, haloalkylcarbonyl, benzyl, phenyl, phenylcarbonyl, alkylsulfonyl, or haloalkylsulfonyl; or the enantiomers or diastereomers or salts thereof, processes for the preparation of compounds of formula (I), use of compounds of formula (I) for combating insects, acarids, or nematodes, and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites using compounds of formula (I).
    • 式(I)的二氰基链烷酸酰胺,其中R 1是H,烷基,卤代烷基,烯基,卤代烯基,炔基或卤代炔基; R 2是H,CN,烷基,卤代烷基,烯基,卤代烯基,炔基,卤代炔基,环烷基,卤代环烷基,烷氧基或卤代烷氧基。 R 3和R 4是H,烷基,卤代烷基,烯基,卤代烯基,炔基,卤代炔基,环烷基,卤代环烷基,环烯基,卤代环烯基或R 3, SO 2和R 4一起可以是亚烷基,卤代亚烷基,亚烯基或卤代亚烯基; X是O或S; R 5和R 6是H,烷基,任选被1至3个基团CN,NO 2,OH,NR 7取代 烷氧基,卤代烷氧基,烷硫基,卤代烷硫基,环烷基,卤代环烷基和任意取代的苯基; 或卤代烷基,环烷基,卤代环烷基,烯基,卤代烯基,炔基,卤代炔基,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,NR 8 R 8,烷氧基羰基,卤代烷氧基羰基,烯氧基羰基,卤代链烯氧基羰基, 烷基羰基,卤代烷基羰基,R 7 R 8 NC(= O) - ,苯基羰基,苄基羰基或苯基,其中苯基羰基,苄基羰基和苯基任选被取代; 或R 5和R 6是饱和的,部分不饱和的或不饱和的5至6元杂环基,其可以含有1至4个选自氧,氮和硫的杂原子 并且该基团可以通过羰基(C(= O))键键合,并且该基团任选被取代; R 7,R 8是H,烷基,卤代烷基,烷基羰基,卤代烷基羰基,苄基,苯基,苯基羰基,烷基磺酰基或卤代烷基磺酰基; 或其对映体或非对映异构体或其盐,式(I)化合物的制备方法,式(I)化合物用于防治昆虫,螨虫或线虫的用途,以及用于治疗,控制,预防或保护动物的方法 使用式(I)化合物对寄生虫的感染或感染。