AR060253A1 - COMPUESTOS DE 3-AMINO-1, 2-BENZISOTIAZOL PARA COMBATIR PESTES ANIMALES, COMPOSICIONES PESTICIDAS Y SEMILLAS QUE LOS COMPRENDEN Y METODOS DE CONTROL DE PESTES ANIMALES Y DE PROTECCIoN DE PLANTAS QUE LOS UTILIZAN. - Google Patents
COMPUESTOS DE 3-AMINO-1, 2-BENZISOTIAZOL PARA COMBATIR PESTES ANIMALES, COMPOSICIONES PESTICIDAS Y SEMILLAS QUE LOS COMPRENDEN Y METODOS DE CONTROL DE PESTES ANIMALES Y DE PROTECCIoN DE PLANTAS QUE LOS UTILIZAN.Info
- Publication number
- AR060253A1 AR060253A1 ARP070101370A ARP070101370A AR060253A1 AR 060253 A1 AR060253 A1 AR 060253A1 AR P070101370 A ARP070101370 A AR P070101370A AR P070101370 A ARP070101370 A AR P070101370A AR 060253 A1 AR060253 A1 AR 060253A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- amino
- alkoxy
- group
- cycloalkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000000203 mixture Substances 0.000 title abstract 3
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 title 1
- 239000000575 pesticide Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 12
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 7
- -1 cyano, nitro, amino Chemical group 0.000 abstract 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 4
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 3
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 3
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- WIJQCPIRWXSWQG-UHFFFAOYSA-N 1,2-benzothiazol-3-amine Chemical class C1=CC=C2C(N)=NSC2=C1 WIJQCPIRWXSWQG-UHFFFAOYSA-N 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
- C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
Compuestos insecticidas de la formula 1 y sus derivados imino isomeros, los enantiomeros, diastereomeros y sales de los mismos y composiciones, que comprenden tales compuestos. Uso de los compuestos de 3-amino-1,2-benzisotiazol, de sus sales o de composiciones, que comprenden los mismos para combatir pestes animales. Además, métodos de aplicar tales compuestos. Reivindicacion 1: Compuestos de 3-amino-1,2-benzisotiazol caracterizados porque tienen la formula 1 en donde n es 0, 1 o 2; R1 es seleccionado entre alquilo C1-6, haloalquilo C1-6, aIquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquiniIo C2-6, cicloalquilo C3-8, halocIcloalquilo C3-6, alcoxi C1-6, haloalcoxi C1-6, pudiendo los radicales mencionados ser no sustituidos o llevar 1, 2 o 3 radicales, seleccionados del grupo, que abarca ciano, nitro, amino, alcoxi C1-4, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, haloalcoxi C1-4, haloalquiltio C1-4, alcoxi C1-4carbonilo, alquil C1-4amino, di(alquil C1- 4)amino, aminocarbonilo, (alquil C1-4)aminocarbonilo, di(alquil C1-4)aminocarbonilo, cicloalquilo C3-8 y fenilo, siendo posible que el fenilo sea no sustituido o esté parcial o completamente halogenado y/o lleve 1, 2 o 3 sustituyentes, seleccionados, independientemente entre si del grupo, que abarca CN, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 y haloalcoxi C1-4 y R2, R3 y R4 son seleccionados, independientemente entre si, del grupo, que abarca hidrogeno, halogeno, ciano, azido, nitro, alquilo C1-6, cicloalquilo C3-8, haloalquilo C1-4, alcoxi C1-4, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, haloalcoxi C1-4, haloalquiltio C1-4, alquenilo C2-6, alquinilo C2-6, (alcoxi C1-4)carbonilo, amino, (alquil C1- 4)amino, di(alquil C1-4)amino, aminocarbonilo, (alquil C1-4)aminocarbonilo, di(alquil C1-4)aminocarbonilo, sulfonilo, sulfonilamino, sulfenilamino, sulfanilamino y C(=O)R2a o C(=O)R3a o C(=O)-R4a, y en donde, R2a o R3a o R4a son seleccionados del grupo, que abarca hidrogeno, hidroxi, alcoxi C1-6, amino, alquilo C1-6, arilo, aril-C1-6-alquilo, (alquil C1-6)-amino, di-(alquil C1-6)-amino, de tres a siete miembros heteroarilo o heteroaril-C1-4-alquilo, conteniendo el anillo heteroarilo como miembros de anillo 1, 2 o 3 heteroátomos, seleccionados del grupo, que abarca nitrogeno, oxigeno, azufre, un grupo SO, SO2 o NR2b o NR3b o NR4b, y en donde R2b o R3b o R4b significan hidrogeno, alquilo C1-6 o (alquil C1-6)-carbonilo; R5 es seleccionado del grupo, que comprende hidrogeno, OR5a, alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-10, aril-C1-4-alquilo, hetaril-C1-4-alquilo, heterociclil-C1-4-alquilo, pudiendo estos radicales ser no sustituidos o estar parcial o completamente halogenados y/o llevar 1-4 radicales seleccionados del grupo, que abarca alcoxi C1-10, alquiltio C1-10,alquilsulfinilo C1-10, alquilsulfonilo C1-10, haloalcoxi C1-10, haloalquiltio C1-10, ( alcoxi C1-10)carbonilo, ciano, nitro, amino, (alquil C1-10)amino, di-(alquil C1-10)amino, cicloalquilo C3-10 y fenilo, siendo posible que el fenilo sea no sustituido o esté parcial o completamente halogenado y/o lleve 1-3 sustituyentes seleccionados del grupo, que abarca CN, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, y en donde R5a es seleccionado entre hidrogeno, alquilo C1-10, acilo C1-10, cicloalquilo C3-10, alquenilo C2-10, alquinilo C2-10, arilo, aril-C1-4-alquilo, heteroarilo y heteroaril-C1-4- alquilo, heterociclilo o heterociclil-C1-4-alquilo y ciclilo, pudiendo todos los radicales ser no sustituidos, estar parcial o completamente halogenados y/o llevar 1, 2 o 3 radicales, seleccionados del grupo, que abarca ciano, nitro, amino, alcoxi C1-4, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, haloalcoxi C1-4, haloalquiltio C1-4, (alcoxi C1-4)carbonilo, (alquil C1-4)amino, di(alquil C1-4)amino y cicloalquilo C3-8; o los enantiomeros, diastereomeros o sales de los mismos, siendo preciso que si n es 0, R5 no es hidrogeno.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US78780906P | 2006-03-31 | 2006-03-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR060253A1 true AR060253A1 (es) | 2008-06-04 |
Family
ID=38229118
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070101370A AR060253A1 (es) | 2006-03-31 | 2007-03-30 | COMPUESTOS DE 3-AMINO-1, 2-BENZISOTIAZOL PARA COMBATIR PESTES ANIMALES, COMPOSICIONES PESTICIDAS Y SEMILLAS QUE LOS COMPRENDEN Y METODOS DE CONTROL DE PESTES ANIMALES Y DE PROTECCIoN DE PLANTAS QUE LOS UTILIZAN. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8017554B2 (es) |
| EP (1) | EP2003975B1 (es) |
| JP (1) | JP2009531374A (es) |
| AR (1) | AR060253A1 (es) |
| AT (1) | ATE448688T1 (es) |
| BR (1) | BRPI0710215A2 (es) |
| DE (1) | DE602007003332D1 (es) |
| ES (1) | ES2335318T3 (es) |
| PE (1) | PE20080052A1 (es) |
| TW (1) | TW200808750A (es) |
| UY (1) | UY30252A1 (es) |
| WO (1) | WO2007113119A1 (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1954138A2 (en) * | 2005-11-21 | 2008-08-13 | Basf Se | Insecticidal methods using 3-amino-1,2-benzisothiazole derivatives |
| ES2383101T3 (es) | 2007-01-26 | 2012-06-18 | Basf Se | Compuestos de 3-amino-1,2-bencisotiazol para combatir plagas animales II |
| DE102007024575A1 (de) * | 2007-05-25 | 2008-11-27 | Bayer Cropscience Ag | Insektizide Zusammensetzungen von 2-Cyanobenzolsulfonamidverbindungen und ihrer isomeren Formen mit verbesserter Wirkung |
| EP2123159A1 (de) | 2008-05-21 | 2009-11-25 | Bayer CropScience AG | (1,2-Benzisothiazol-3-yl)(thio)carbamate und (1,2-Benzisothiazol-3-yl)(thio)oxamate und deren Oxidationsformen als Pestizide |
| CN102066368A (zh) * | 2008-06-18 | 2011-05-18 | 巴斯夫欧洲公司 | 用于防治动物害虫的1,2-苯并异噻唑化合物 |
| GB0820710D0 (en) * | 2008-11-12 | 2008-12-17 | Syngenta Participations Ag | Chemical compounds |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1545842C3 (de) | 1965-07-28 | 1974-09-19 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von N-substituierten 3-Halogen-benzisothiazoliumhalogeniden |
| DE1670920A1 (de) | 1967-09-09 | 1971-04-01 | Bayer Ag | N-Disubstituierte 3-Amino-1,2-benzisothiazol-Derivate |
| DE1667970A1 (de) | 1968-02-29 | 1971-07-22 | Basf Ag | Schaedlingsbekaempfungsmittel |
| NL6802841A (es) * | 1968-02-29 | 1969-09-02 | ||
| DE1915387A1 (de) * | 1969-03-26 | 1970-10-01 | Basf Ag | Herbizid |
| DE2803755A1 (de) * | 1978-01-28 | 1979-08-02 | Bayer Ag | Verfahren zur herstellung von n-substituierten 3-amino-1.2-benzisothiazolen |
| EP0033984B1 (en) * | 1980-01-23 | 1984-06-06 | Duphar International Research B.V | New sulphonyl compounds, method of preparing the new compounds, as well as aphicidal compositions on the basis of the new compounds |
| US4492705A (en) | 1982-02-12 | 1985-01-08 | Ciba-Geigy Corporation | 3-Amidino-benzisothiazole-1,1-dioxides and their use for controlling pests |
| DE3382093D1 (de) * | 1982-11-26 | 1991-02-07 | Ciba Geigy Ag | Schaedlingsbekaempfungsmittel. |
| EP0133418A3 (de) * | 1983-08-09 | 1985-04-03 | Ciba-Geigy Ag | Die Verwendung von 3-Acylaminobenzisothiazolen in der Schädlingsbekämpfung |
| DE3478986D1 (en) | 1983-09-14 | 1989-08-24 | Ciba Geigy Ag | Pesticide |
| DE3343091A1 (de) * | 1983-11-29 | 1985-06-05 | Bayer Ag, 5090 Leverkusen | Verwendung von 3-amino-1,2-benzisothiazolen als mikrobizide zum schutz technischer materialien |
| DE3544436A1 (de) | 1984-12-18 | 1986-06-19 | Ciba-Geigy Ag, Basel | Neue dioxide |
| ZA861026B (en) | 1985-02-13 | 1986-09-24 | Ciba Geigy Ag | Pesticidal compositions |
| DE3607343A1 (de) | 1985-03-19 | 1986-09-25 | Dr. Karl Thomae Gmbh, 88400 Biberach | Verfahren zur herstellung von 4-hydroxy-1,2-benzisothiazol-3(2h)-on-1,1-dioxid und seinen salzen |
| EP0207891A1 (de) | 1985-06-14 | 1987-01-07 | Ciba-Geigy Ag | Salze von 3-Acylaminobenzisothiazol-S,S-dioxiden, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung |
| JPH01319467A (ja) * | 1988-06-20 | 1989-12-25 | Ishihara Sangyo Kaisha Ltd | ベンゾイソチアゾール系化合物、それらの製造方法及びそれらを含有する殺虫剤 |
| DE3922088A1 (de) * | 1989-07-05 | 1991-01-17 | Basf Ag | 3-anilino-benzisothiazole und diese enthaltende fungizide |
| JPH06220030A (ja) | 1993-01-22 | 1994-08-09 | Sumitomo Pharmaceut Co Ltd | ３−アミノ−１，２−ベンズイソチアゾール誘導体の製造法 |
| DE59900096D1 (de) * | 1998-03-25 | 2001-06-28 | Basf Ag | Verfahren zur Herstellung von Saccharincarbonsäurehalogeniden |
| WO2003087072A1 (en) | 2002-03-29 | 2003-10-23 | Mochida Pharmaceutical Co., Ltd. | Therapeutic agent for endothelial disorder |
| UA79404C2 (en) * | 2003-10-02 | 2007-06-11 | Basf Ag | 2-cyanobenzenesulfonamide for controlling pests |
| JP2008531596A (ja) * | 2005-02-25 | 2008-08-14 | ライジェル ファーマシューティカルズ， インコーポレイテッド | Ｈｃｖ感染を治療または予防するのに有用なベンゾイソチアゾール |
| CN101277939A (zh) * | 2005-09-09 | 2008-10-01 | 布里斯托尔-迈尔斯斯奎布公司 | 无环ikur抑制剂 |
| EP1954138A2 (en) * | 2005-11-21 | 2008-08-13 | Basf Se | Insecticidal methods using 3-amino-1,2-benzisothiazole derivatives |
| ES2383101T3 (es) | 2007-01-26 | 2012-06-18 | Basf Se | Compuestos de 3-amino-1,2-bencisotiazol para combatir plagas animales II |
-
2007
- 2007-03-22 BR BRPI0710215-1A patent/BRPI0710215A2/pt not_active IP Right Cessation
- 2007-03-22 DE DE602007003332T patent/DE602007003332D1/de active Active
- 2007-03-22 JP JP2009502032A patent/JP2009531374A/ja not_active Ceased
- 2007-03-22 AT AT07727214T patent/ATE448688T1/de not_active IP Right Cessation
- 2007-03-22 US US12/294,753 patent/US8017554B2/en not_active Expired - Fee Related
- 2007-03-22 EP EP07727214A patent/EP2003975B1/en active Active
- 2007-03-22 WO PCT/EP2007/052738 patent/WO2007113119A1/en not_active Ceased
- 2007-03-22 ES ES07727214T patent/ES2335318T3/es active Active
- 2007-03-30 AR ARP070101370A patent/AR060253A1/es not_active Application Discontinuation
- 2007-03-30 TW TW096111451A patent/TW200808750A/zh unknown
- 2007-03-30 PE PE2007000391A patent/PE20080052A1/es not_active Application Discontinuation
- 2007-04-02 UY UY30252A patent/UY30252A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2003975A1 (en) | 2008-12-24 |
| BRPI0710215A2 (pt) | 2011-08-02 |
| ATE448688T1 (de) | 2009-12-15 |
| UY30252A1 (es) | 2007-05-31 |
| US20100167922A1 (en) | 2010-07-01 |
| PE20080052A1 (es) | 2008-04-06 |
| US8017554B2 (en) | 2011-09-13 |
| JP2009531374A (ja) | 2009-09-03 |
| ES2335318T3 (es) | 2010-03-24 |
| TW200808750A (en) | 2008-02-16 |
| EP2003975B1 (en) | 2009-11-18 |
| WO2007113119A1 (en) | 2007-10-11 |
| DE602007003332D1 (de) | 2009-12-31 |
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