AR057996A1 - Compuestos, composiciones pesticidas y metodo par combatir pestes - Google Patents
Compuestos, composiciones pesticidas y metodo par combatir pestesInfo
- Publication number
- AR057996A1 AR057996A1 ARP060105757A ARP060105757A AR057996A1 AR 057996 A1 AR057996 A1 AR 057996A1 AR P060105757 A ARP060105757 A AR P060105757A AR P060105757 A ARP060105757 A AR P060105757A AR 057996 A1 AR057996 A1 AR 057996A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- radicals
- amino
- alkoxy
- alkenyl
- Prior art date
Links
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
- C07D417/12—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
Compuestos de 1-(azolin-2-il)-amino-alcano, que son utiles para combatir insectos, arácnidos y nemátodos. También un método para combatir pestes animales seleccionados entre insectos, arácnidos y nemátodos, y una composicion para combatir pestes animales. Reivindicacion 1: Compuestos de 1-(azolin-2-il)-amino-1-fenil-2-hetaril-etano, caracterizados porque tiene la formula general (1), en donde R1, R2, R3 son seleccionados entre hidrogeno, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, pudiendo los átomos de carbono en los radicales alifáticos de los grupos arriba mencionados llevar cualquier combinacion de uno, dos o tres radicales, seleccionados, independientemente entre sí, del grupo que comprende: halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alqueniloxi C2-6, aIquiniloxi C2-6, haloalcoxi C1-6, haloalquilo C1-6 y alquiltio C1-6; fenilo o bencilo, cada uno sustituido o no sustituido con cualquier combinacion de uno a cinco grupos de halogeno, uno a tres alquilo C1-6, haloalquilo C1-6, alquiltio C1-6, haloalquiltio C1-6, alcoxi C1-6 o haloalcoxi C1-6 grupos; A es un radical de las formulas A1 o A2, en donde X es azufre o oxígeno; R4a, R4b, R4c, R4d son seleccionados, independientemente entre sí, de hidrogeno, halogeno, alquilo C1-6, haloalquilo C1-6, alquilamino C1-6, alcoxi C1-6, cicloalquilo C3-6, pudiendo los átomos de carbono en los radicales alifáticos de los grupos arriba mencionados llevar cualquier combinacion de uno, dos o tres radicales, seleccionados, independientemente entre sí, del grupo que comprende halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6, haloalquilo C1-6 y alquiltio C1-6; R5, R6, R9 son seleccionados, independientemente entre sí, de hidrogeno, ciano, nitro, formilo, C(=O)R5c o C(=O)R6c o C(=O)R9c, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-8, alcoxi C1-6, (alcoxi C1-6)metileno, alquilsulfinilo C1-6, alquilsulfenilo C1-6 o alquilsulfonilo C1-6, pudiendo los átomos de carbono en los radicales alifáticos de los grupos arriba mencionados llevar cualquier combinacion de 1, 2 o 3 radicales, seleccionados independientemente entre sí, del grupo que comprende: halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6; C(O)NR5aR5b o C(O)NR6aR6b o C(O)NR9aR9b, (SO2)NR5aR5b, (SO2)NR6aR6b o (SO2)NR9aR9b, fenilo, feniloxi o bencilo, pudiendo cada uno de los tres ultimos radicales mencionados ser no sustituidos o sustituidos con 1 a 5 radicales, seleccionados, independientemente entre sí, del grupo que comprende: uno a cinco radicales halogeno, uno a tres radicales alquilo C1-6, uno a tres radicales haloalquilo C1-6, uno a tres radicales alquiltio C1-6, uno a tres radicales haloalquiltio C1-6, uno a tres radicales alcoxi C1-6 y. uno a tres radicales haloalcoxi C1-6; y en donde R5a, R6a, R9a, R5b, R6b, R9b, R5c,R6c y R9c tienen las definiciones abajo indicadas; B es un sistema de anillo fenilo opcionalmente sustituido W es un anillo heteroaromático de cinco a seis miembros, que puede contener 1 a 4 heteroátomos seleccionados entre oxígeno, nitrogeno y azufre, donde el anillo heteroaromático puede estar condensado, opcionalmente, con un anillo seleccionado entre fenilo y un anillo heterocíclico aromático saturado, parcialmente insaturado de 5 a 6 miembros, que puede contener 1 a 3 heteroátomos seleccionados entre oxígeno, nitrogeno y azufre, y donde el anillo heteroaromático de cinco a seis miembros o los respectivos sistemas de anillo condensados pueden ser no sustituidos u, opcionalmente, estar sustituidos por R9 y/o cualquier combinacion de 1 a 4 grupos R8 (formula (2)), donde n es 0, 1, 2, 3, o 4; y R8 tiene las definiciones abajo indicadas; y R9 tiene las definiciones arriba indicadas y en donde R8 es seleccionado entre halogeno, OH, SH, NH2, SO3H, COOH, ciano, azido, nitro, formilo, CONH2, CSNH2, CH=N-OH, CH=N-O-(C1-C6)-alquilo C1-6, C(=O)R8c, C(=S)R8c, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-8, alquilamino C1-6, alquenilamino C2-6, alquinilamino C2-6, di(alquil C1-6)amino, di(alquenil C2-6)amino, di(alquinil C2-6)amino, alquiltio C1-6, alqueniltio C2-6, alquiniltio C2-6, alquilsulfonilo C1-6, alquenilsulfonilo C2-6, alquinilsulfonilo C2-6, (alquil C1-6)carbonilo, (alquenil C2-6)-carbonilo, (alquinil C2-6)-carbonilo, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, (alcoxi C1-6)carbonilo, (alqueniloxi C2-6)carbonilo, (alquiniloxi C2-6)- carbonilo, (alquil C1-6)carboniloxi, (alquenil C2-6)carbonil-oxi, (alquinil C2-6)carboniloxi, (alquil C1-6)carbonil-amino, (alquenil C2-6)carbonil-amino, (alquinil C2-6)carbonil-amino, pudiendo los átomos de carbono en los radicales alifáticos de los grupos arriba mencionados llevar cualquier combinacion de uno, dos o tres radicales, seleccionados, independientemente entre sí, del grupo que comprende: halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6, haloalquilo C1-6 y alquiltio C1-6; C(O)NR8aR8b, (SO2)NR8aR8b; donde R8a, R8b y R8c tienen las definiciones abajo indicadas, un radical Y-Ar o un radical Y-Cy, en donde Y es un enlace simple, O, S, NH, alcanodiilo C1-6 o alcanodiiloxi C1-6; Ar es fenilo, naftilo o un anillo heteroaromático mono o bicíclico de 5 a 10 miembros, que contiene 1, 2, 3 o 4 heteroátomos seleccionados entre 1 o 2 átomos de oxígeno 1 o 2 átomos de azufre y 1 a 3 átomos de nitrogeno como miembros de anillo, donde Ar no lleva sustituyente o puede llevar cualquier combinacion de uno a cinco radicales, seleccionados, independientemente entre sí, del grupo que comprende: halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6; Cy es cicloalquilo C3-12, que es no sustituido o sustituido con :uno a cinco radicales, seleccionados, independientemente entre sí, del grupo que comprende halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6; y en donde R5a, R6a, R8a y R5b, R6b, R8b son seleccionados, independientemente entre sí, de: hidrogeno, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, o alquinilo C2-6, pudiendo los átomos de carbono en los radicales alifáticos de los grupos arriba mencionados llevar cualquier combinacion de uno, dos o tres radicales, seleccionados, independientemente entre sí, del grupo que comprende halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6, haloalquilo C1-6 y alquiltio C1-6; y R5c, R6c, R8c y R9c son seleccionados, independientemente, entre sí de: hidrogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3- 8, alquiltio C1-6, alcoxi C1-6, (alquil C1-6)amino, di(alquil C1-6)amino, hidracino, (alquil C1-6)hidracino, di(alquil C1-6)hidracino, fenilo y heteroarilo, que puede ser un anillo heteroaromático mono o bicíclico de 5 a 10 miembros, que contiene 1, 2, 3 o 4 heteroátomos seleccionados entre O, S y N o los enantiomeros, diastereomeros o sales de los mismos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US75336705P | 2005-12-22 | 2005-12-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR057996A1 true AR057996A1 (es) | 2008-01-09 |
Family
ID=37836703
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060105757A AR057996A1 (es) | 2005-12-22 | 2006-12-21 | Compuestos, composiciones pesticidas y metodo par combatir pestes |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US20080312085A1 (es) |
| EP (1) | EP1968974A1 (es) |
| JP (1) | JP2009520746A (es) |
| KR (1) | KR20080081052A (es) |
| CN (1) | CN101346374A (es) |
| AP (1) | AP2008004547A0 (es) |
| AR (1) | AR057996A1 (es) |
| AU (1) | AU2006328589A1 (es) |
| BR (1) | BRPI0620200A2 (es) |
| CA (1) | CA2631148A1 (es) |
| CR (1) | CR10117A (es) |
| EC (1) | ECSP088606A (es) |
| IL (1) | IL191572A0 (es) |
| MA (1) | MA30148B1 (es) |
| PE (1) | PE20071001A1 (es) |
| RU (1) | RU2008129627A (es) |
| TW (1) | TW200734330A (es) |
| UA (1) | UA91395C2 (es) |
| UY (1) | UY30063A1 (es) |
| WO (1) | WO2007071585A1 (es) |
| ZA (1) | ZA200806257B (es) |
Families Citing this family (70)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7989394B2 (en) | 2006-06-30 | 2011-08-02 | Basf Se | Substituted 1-(azolin-2-yl)-amino-2-aryl-1-hetaryl-ethane compounds |
| JP2010513374A (ja) * | 2006-12-21 | 2010-04-30 | ビーエーエスエフ ソシエタス・ヨーロピア | 害虫駆除のための置換1−(アゾリン−2−イル)−アミノ−1,2−ヘテロシクリル−エタン化合物 |
| US8153560B2 (en) | 2007-03-01 | 2012-04-10 | Basf Se | Pesticidal active mixtures comprising aminothiazoline compounds |
| EP1992228A1 (en) * | 2007-05-14 | 2008-11-19 | Bayer CropScience AG | Insecticidal substituted thiourea derivatives |
| CA2691573A1 (en) | 2007-07-03 | 2009-01-08 | Basf Se | 1-(azolin-2-yl)amino-1,2-diphenylethane compounds for combating animal pests |
| CA2712190A1 (en) * | 2008-01-18 | 2009-07-23 | Allergan, Inc. | Oxazolidine and thiazolidine selective subtype alpha 2 adrenergic agents and methods for use thereof |
| US8809379B2 (en) * | 2008-01-18 | 2014-08-19 | Allergan, Inc. | Selective subtype alpha 2 adrenergic agents and methods for use thereof |
| WO2009153238A1 (en) * | 2008-06-20 | 2009-12-23 | Basf Se | Aminothiazoline compounds for combating insects, arachnids and nematodes |
| WO2010007060A1 (en) * | 2008-07-17 | 2010-01-21 | Basf Se | Azolin-2-ylamino compounds for combating animal pests |
| US8695707B2 (en) * | 2009-06-16 | 2014-04-15 | Schlumberger Technology Corporation | Asphaltene removal composition and methods |
| JP2013503169A (ja) * | 2009-08-28 | 2013-01-31 | ビー・エイ・エス・エフ、コーポレーション | 発泡性駆除薬組成物および施用方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4419587A1 (de) * | 1994-06-03 | 1995-12-07 | Bayer Ag | Heterocyclische Imino-Derivate |
| US6482840B2 (en) * | 2000-05-22 | 2002-11-19 | Merck & Co., Inc. | Substituted cyclic amidine derivatives as inhibitors of cell adhesion |
| WO2005063724A1 (en) * | 2003-12-23 | 2005-07-14 | Basf Aktiengesellschaft | 1-(azolin-2-yl) amino-1,2-diphenylethane compounds for combatting insects, arachnids and nematodes |
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2006
- 2006-12-11 UA UAA200809261A patent/UA91395C2/ru unknown
- 2006-12-11 WO PCT/EP2006/069525 patent/WO2007071585A1/en not_active Ceased
- 2006-12-11 KR KR1020087017743A patent/KR20080081052A/ko not_active Withdrawn
- 2006-12-11 PE PE2006001578A patent/PE20071001A1/es not_active Application Discontinuation
- 2006-12-11 AP AP2008004547A patent/AP2008004547A0/xx unknown
- 2006-12-11 CN CNA2006800485307A patent/CN101346374A/zh active Pending
- 2006-12-11 US US12/158,261 patent/US20080312085A1/en not_active Abandoned
- 2006-12-11 JP JP2008546368A patent/JP2009520746A/ja not_active Withdrawn
- 2006-12-11 CA CA002631148A patent/CA2631148A1/en not_active Abandoned
- 2006-12-11 EP EP06830499A patent/EP1968974A1/en not_active Withdrawn
- 2006-12-11 RU RU2008129627/04A patent/RU2008129627A/ru not_active Application Discontinuation
- 2006-12-11 BR BRPI0620200A patent/BRPI0620200A2/pt not_active IP Right Cessation
- 2006-12-11 AU AU2006328589A patent/AU2006328589A1/en not_active Abandoned
- 2006-12-21 AR ARP060105757A patent/AR057996A1/es unknown
- 2006-12-22 UY UY30063A patent/UY30063A1/es unknown
- 2006-12-22 TW TW095148529A patent/TW200734330A/zh unknown
-
2008
- 2008-05-20 IL IL191572A patent/IL191572A0/en unknown
- 2008-06-26 CR CR10117A patent/CR10117A/es not_active Application Discontinuation
- 2008-07-07 EC EC2008008606A patent/ECSP088606A/es unknown
- 2008-07-07 MA MA31093A patent/MA30148B1/fr unknown
- 2008-07-18 ZA ZA200806257A patent/ZA200806257B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2006328589A1 (en) | 2007-06-28 |
| PE20071001A1 (es) | 2007-10-26 |
| US20080312085A1 (en) | 2008-12-18 |
| IL191572A0 (en) | 2008-12-29 |
| UA91395C2 (ru) | 2010-07-26 |
| TW200734330A (en) | 2007-09-16 |
| JP2009520746A (ja) | 2009-05-28 |
| CN101346374A (zh) | 2009-01-14 |
| CA2631148A1 (en) | 2007-06-28 |
| AP2008004547A0 (en) | 2008-08-31 |
| MA30148B1 (fr) | 2009-01-02 |
| CR10117A (es) | 2008-09-22 |
| ZA200806257B (en) | 2009-12-30 |
| BRPI0620200A2 (pt) | 2016-08-23 |
| UY30063A1 (es) | 2007-07-31 |
| RU2008129627A (ru) | 2010-01-27 |
| ECSP088606A (es) | 2008-08-29 |
| KR20080081052A (ko) | 2008-09-05 |
| EP1968974A1 (en) | 2008-09-17 |
| WO2007071585A1 (en) | 2007-06-28 |
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