AR058203A1 - Metodos insecticidas que utilizan derivados de 3- amino -1,2- bencisotiazol - Google Patents
Metodos insecticidas que utilizan derivados de 3- amino -1,2- bencisotiazolInfo
- Publication number
- AR058203A1 AR058203A1 ARP060105080A ARP060105080A AR058203A1 AR 058203 A1 AR058203 A1 AR 058203A1 AR P060105080 A ARP060105080 A AR P060105080A AR P060105080 A ARP060105080 A AR P060105080A AR 058203 A1 AR058203 A1 AR 058203A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- amino
- alkoxy
- group
- haloalkoxy
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 6
- 239000002917 insecticide Substances 0.000 title 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 14
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 13
- 125000000217 alkyl group Chemical group 0.000 abstract 13
- -1 cyano, azido, amino Chemical group 0.000 abstract 10
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 7
- 241000238631 Hexapoda Species 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 5
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 4
- 241000239223 Arachnida Species 0.000 abstract 4
- 241000244206 Nematoda Species 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 4
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 3
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 3
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 3
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl 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
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 239000002689 soil Substances 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 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 1
- 206010061217 Infestation Diseases 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 1
- 238000009395 breeding Methods 0.000 abstract 1
- 230000001488 breeding effect Effects 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
- 150000007971 urates Chemical class 0.000 abstract 1
Classifications
-
- 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
-
- 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
-
- 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
- C07D417/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/06—Peri-condensed systems
Abstract
Métodos insecticidas que utilizan compuestos de 3-amino-1,2-bencisotiazol de formula (1). Métodos de combatir o reprimir insectos, arácnidos o nematodos, métodos para proteger las plantas en crecimiento contra el ataque o la infestacion por insectos, arácnidos o nematodos, y métodos para la proteccion de las semillas contra los insectos del suelo y de las raíces y brotes de las plantas jovenes contra insectos del suelo y de las hojas. Reivindicacion 1: Un método para combatir o reprimir insectos, arácnidos o nematodos caracterizado porque comprende poner en contacto un insecto, arácnido o nematodo o su suministro de alimentacion, hábitat o suelos de reproduccion con una cantidad eficaz como plaguicida de al menos un compuesto de 3-amino-1,2-bencisotiazol de la formula (1) o una composicion que comprende al menos un compuesto de formula (1) en donde: n es 0, 1 o 2; R1 es H, nitro, ciano, azido, amino, halogeno, sulfonilamino, sulfenilamino, sulfinilamino, C(=O)R1a, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-8, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, (alquil C1-6)amino, di(alquil C1-6)amino, alquilsulfinilo C1-6 o alquilsulfonilo C1-6, en donde los once ultimos radicales mencionados pueden estar insustituidos, parcial o totalmente halogenados y/o pueden llevar 1, 2 o 3 radicales, seleccionados del grupo constituido por 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, cicloalquilo C3-8 y fenilo, siendo posible que fenilo esté insustituido, parcial o totalmente halogenado y/o lleve 1, 2 o 3 sustituyentes, seleccionados independientemente unos de otros del grupo constituido por alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 y haloalcoxi C1-4, en donde R1a se selecciona del grupo constituido por H, alcoxi C1-6, amino, (alquil C1-6)amino, di(alquil C1- 6)amino, alquilo C1-6, arilo, aril-alquilo C1-6, heteroarilo de 3 a 7 miembros o heteroaril-alquilo C1-4, en donde el anillo heteroarilo contiene como miembros del anillo 1, 2 o 3 heteroátomos seleccionados del grupo constituido por N, O, S, un grupo SO, SO2 o N-Rn, en donde Rn es H, alquilo C1-6 o (alquil C1-6)carbonilo; R2, R3 y R4 se seleccionan, independientemente unos de otros, del grupo constituido por H, 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, (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 se seleccionan del grupo constituido por H, hidroxi, alcoxi C1-6, amino, alquilo C1-6, arilo, aril-alquilo C1-6, (alquil C1-6)amino, di(alquil C1-6)amino, heteroarilo de 3 a 7 miembros o heteroaril-alquilo C1-4, en donde el anillo heteroarilo contiene como miembros de anillo 1, 2 o 3 heteroátomos, seleccionados del grupo constituido por N, O, S, un grupo SO, SO2 o N-Rn, en donde Rn es H, alquilo C1-6 o (alquil C1-6)carbonilo; R5 se selecciona del grupo constituido por OR5a, alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-10, en donde estos radicales pueden estar insustituidos, parcial o totalmente halogenados y/o pueden llevar 1-4 radicales seleccionados del grupo constituido por 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 fenilo esté insustituido, parcial o totalmente halogenado y/o lleve 1-3 sustituyentes, seleccionados del grupo constituido por alquilo C1-6, haloalquilo C1-6, alcoxi C1-6 y haloalcoxi C1-6 y en donde R5a se selecciona de H, alquilo C1-10, acilo C1-10, cicloalquilo C3-10, alquenilo C2-10, alquinilo C2-10, arilo, aril-alquilo C1-4, heteroarilo y heteroaril- alquilo C1-4, heterociclilo o heterociclil-alquilo C1-4 y en donde los átomos de C de los radicales pueden estar insustituidos, parcial o totalmente halogenados y/o pueden llevar 1, 2 o 3 radicales seleccionados del grupo constituido por 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; R6 se selecciona del grupo constituido por alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-10, en donde los cuatro ultimos radicales mencionados pueden estar insustituidos, parcial o totalmente halogenados y/o peden llevar 1-4 radicales seleccionados del grupo constituido por 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 fenilo esté insustituido, parcial o totalmente halogenado y/o lleve 1-3 sustituyentes seleccionados del grupo constituido por alquilo C1-6, haloalquilo C1-6, alcoxi C1-6 y haloalcoxi C1-6, o R5/R5a y R6 pueden unirse para formar un anillo de 3-10 miembros, opcionalmente sustituido y que contiene opcionalmente, además de alquilo C1-5 opcionalmente sustituido, independientemente 1 a 3 restos N, NRn, O, S, SO, SO2, que pueden ser opcionalmente insaturados, y en donde Rn es H, alquilo C1-6 o (alquil C1-6)carbonilo; o los enantiomeros o diastereoisomeros, sales o ésteres del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73844305P | 2005-11-21 | 2005-11-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR058203A1 true AR058203A1 (es) | 2008-01-23 |
Family
ID=38048999
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060105080A AR058203A1 (es) | 2005-11-21 | 2006-11-20 | Metodos insecticidas que utilizan derivados de 3- amino -1,2- bencisotiazol |
Country Status (9)
Country | Link |
---|---|
US (1) | US20090069317A1 (es) |
EP (1) | EP1954138A2 (es) |
JP (1) | JP2009516667A (es) |
AR (1) | AR058203A1 (es) |
BR (1) | BRPI0618810A2 (es) |
PE (1) | PE20070847A1 (es) |
TW (1) | TW200803739A (es) |
UY (1) | UY29951A1 (es) |
WO (1) | WO2007057407A2 (es) |
Families Citing this family (117)
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DE1670907B2 (de) * | 1967-08-16 | 1976-07-22 | Bayer Ag, 5090 Leverkusen | N-disubstituierte 3-amino-1,2benzisothiazole und verfahren in ihrer herstellung |
DE1915387A1 (de) * | 1969-03-26 | 1970-10-01 | Basf Ag | Herbizid |
JPS4824735B1 (es) * | 1970-01-26 | 1973-07-24 | ||
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 |
EP0110829B1 (de) * | 1982-11-26 | 1990-12-27 | Ciba-Geigy Ag | Schädlingsbekämpfungsmittel |
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 |
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 |
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 |
US8017554B2 (en) * | 2006-03-31 | 2011-09-13 | Basf Se | 3-amino-1,2-benzisothiazole compounds for combating animal pest |
-
2006
- 2006-11-15 PE PE2006001454A patent/PE20070847A1/es not_active Application Discontinuation
- 2006-11-15 US US12/094,342 patent/US20090069317A1/en not_active Abandoned
- 2006-11-15 EP EP06819483A patent/EP1954138A2/en not_active Withdrawn
- 2006-11-15 JP JP2008540609A patent/JP2009516667A/ja active Pending
- 2006-11-15 BR BRPI0618810A patent/BRPI0618810A2/pt not_active IP Right Cessation
- 2006-11-15 WO PCT/EP2006/068469 patent/WO2007057407A2/en active Application Filing
- 2006-11-20 AR ARP060105080A patent/AR058203A1/es not_active Application Discontinuation
- 2006-11-21 TW TW095142924A patent/TW200803739A/zh unknown
- 2006-11-21 UY UY29951A patent/UY29951A1/es unknown
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BRPI0618810A2 (pt) | 2016-11-22 |
EP1954138A2 (en) | 2008-08-13 |
JP2009516667A (ja) | 2009-04-23 |
WO2007057407A2 (en) | 2007-05-24 |
TW200803739A (en) | 2008-01-16 |
WO2007057407A3 (en) | 2007-11-29 |
UY29951A1 (es) | 2007-06-29 |
PE20070847A1 (es) | 2007-09-21 |
US20090069317A1 (en) | 2009-03-12 |
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