AR076798A1 - Pirazinilpirazoles y composiciones que comprenden dichos compuestos - Google Patents
Pirazinilpirazoles y composiciones que comprenden dichos compuestosInfo
- Publication number
- AR076798A1 AR076798A1 ARP100101827A ARP100101827A AR076798A1 AR 076798 A1 AR076798 A1 AR 076798A1 AR P100101827 A ARP100101827 A AR P100101827A AR P100101827 A ARP100101827 A AR P100101827A AR 076798 A1 AR076798 A1 AR 076798A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- alkoxy
- halogen
- polysubstituted
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 125000003545 alkoxy group Chemical group 0.000 abstract 14
- 125000001188 haloalkyl group Chemical group 0.000 abstract 14
- 229910052736 halogen Inorganic materials 0.000 abstract 12
- 125000005843 halogen group Chemical group 0.000 abstract 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 8
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 7
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 7
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 6
- 125000004414 alkyl thio group Chemical group 0.000 abstract 6
- -1 cyano, formyl Chemical group 0.000 abstract 6
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 abstract 6
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 abstract 6
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 6
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 3
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- XBSVVLLAMHTBPS-UHFFFAOYSA-N 2-(1h-pyrazol-5-yl)pyrazine Chemical class N1N=CC=C1C1=CN=CC=N1 XBSVVLLAMHTBPS-UHFFFAOYSA-N 0.000 abstract 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 2
- 125000005392 carboxamide group Chemical group NC(=O)* 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 125000005432 dialkylcarboxamide group Chemical group 0.000 abstract 2
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000004686 alkyl sulfanyl alkyl group Chemical group 0.000 abstract 1
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 abstract 1
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 abstract 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005225 alkynyloxycarbonyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 230000000590 parasiticidal effect Effects 0.000 abstract 1
- 239000002297 parasiticide Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
- C07D417/14—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 three or more hetero rings
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)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Se desvelan pirazin-2-ilpirazoles, como en el uso de los mismos como insecticidas y/o parasiticidas. Además, se describen procedimientos para su preparacion y composiciones que comprenden dichos pirazin-2-ilpirazoles. Reivindicacion 1: Pirazinilpirazoles de formula general (1) en la que X es fenilo, 2-piridilo o 3-piridilo, cada uno de los cuales está sustituido con uno o más sustituyentes seleccionados entre el grupo constituido por halogeno, alquilo, haloalquilo, alcoxi, alcoxialquilo, alcoxialcoxi, cicloalquilo, alqueniloxi, alquiniloxi, benciloxi, cicloalquilalcoxi, haloalcoxi, haloalcoxialquilo, alquilsulfanilo, haloalquilsulfanilo, alquilsulfinilo, haloalquilsulfinilo, alquilsulfonilo, haloalquilsulfonilo, ciano, nitro, alquilcarbonilo, alcoxicarbonilo, alcoxicarbonilalquilo, carboxilo, carboxamida, dialquilcarboxamida, trialquilsililo, amino, alquilamino, dialquilamino, aIquilsulfonilamino, dialquilsulfonilamino, formilo, -CH=NO-H, -CH=NO-alquilo, -CH=NO-haloalquilo, -C(CH3)=NO-H, -C(CH3)=NO-alquilo, -C(CH3)=NO-haloalquilo; o fenilo, 2-piridilo y 3-piridilo opcionalmente sustituido con uno o más átomos de halogeno, ciano, nitro, alquilo, alcoxi o haloalquilo, donde los grupos alquilo, haloalquilo, alcoxi y/o haloalcoxi vecinos en el sustituyente fenilo, el sustituyente 2-piridilo o el sustituyente 3-piridilo, junto con los átomos de carbono a los que están unidos, pueden formar un sistema cíclico de cinco a siete miembros que contiene de 0 a 2 átomos de oxígeno o nitrogeno, donde dos átomos de oxígeno no están unidos directamente entre sí, y cuyo resto alquilo puede estar opcionalmente sustituido con uno o más átomos de halogeno y/o radicales alquilo adicionales; R1 es hidrogeno, alquilo que está opcionalmente mono- o independientemente polisustituido con alcoxi, haloalcoxi, alquilsulfanilo, haloalquilsulfanilo, alquilsulfinilo, haloalquilsulfinilo, alquilsulfonilo, haloalquilsulfonilo, alquilcarbonilo, alcoxicarbonilo, hidroxilo y/o cicloalquilo; alquenilo que está opcionalmente mono- o independientemente polisustituido con halogeno, alcoxi, haloalcoxi, alquilsulfanilo, haloalquilsulfanilo, alquilsulfinilo, haloalquilsulfinilo, alquilsulfonilo, haloalquilsulfonilo, alquilcarbonilo, alcoxicarbonilo y/o cicloalquilo; cicloalquilo que está opcionalmente mono- o independientemente polisustituido con alquilo, haloalquilo y/o halogeno; haloalquilo que está opcionalmente mono- o independientemente polisustituido con alcoxi, alquilsulfanilo, haloalquilsulfanilo, alquilsulfinilo, haloalquilsulfinilo, alquilsulfonilo, haloalquilsulfonilo y/o fenilo, opcionalmente mono- o independientemente polisustituido con halogeno, alquilo, haloalquilo y/o alcoxi; fenilo que está opcionalmente mono- o independientemente polisustituido con halogeno, alquilo, haloalquilo y/o alcoxi; bencilo que está opcionalmente mono- o independientemente polisustituido con halogeno, alquilo, haloalquilo y/o alcoxi; ciano, formilo, alquilcarbonilo, -CH=NO-H, -CH=NO-alquilo, -CH=NO-haloalquilo, -C(CH3)=NO-H, -C(CH3)=NO-alquilo o -C(CH3)=NO-haloalquilo; R2 es amino opcionalmente sustituido, donde el amino puede estar mono- o independientemente disustituido con alquilo, haloalquilo, alcoxialquilo, alquilsulfanilalquilo, alquilsulfinilalquilo, alquilsulfonilalquilo, alquilcarbonilo, cicloalquilo, cicloalquilalquilo, alquenilo, donde los radicales anteriores están opcionalmente sustituidos con halogeno, ciano, alcoxi, alcoxicarbonilo o fenilo, donde el anillo de fenilo está opcionalmente mono- o polisustituido con uno o más sustituyentes seleccionados independientemente entre halogeno, alquilo, haloalquilo y alcoxi; alquinilo, alcoxicarbonilo, alqueniloxicarbonilo, alquiniloxicarbonilo, alcoxicarbonilalquilo, alcoxicarbonilcarbonilo, heterociclilo, heteroarilo, heterociclilalquilo o heteroarilalquilo, donde el anillo heterocíclico o heteroaromático puede estar opcionalmente mono- o polisustituido con uno o más sustituyentes seleccionados independientemente entre halogeno, alquilo, haloalquilo y alcoxi; bencilo o fenilcarbonilo, donde el anillo de fenilo en el bencilo y fenilcarbonilo está opcionalmente mono- o polisustituido con uno o más sustituyentes seleccionados independientemente entre halogeno, alquilo, haloalquilo y alcoxi; y cada uno de R3 y R4 es independientemente hidrogeno, halogeno, alquilo, cicloalquilo, haloalquilo, ciano, hidroxilo, formilo, alquilcarbonilo, -CH=NO-H, -CH=NO-alquilo, -CH=NO-haloalquilo, -C(CH3)=NOH, -C(CH3)=NO-alquilo, -C(CH3)=NO-haloalquilo, nitro, hidroxilo, SH, alcoxi, alquilsulfanilo, haloalquilsulfanilo, alquilsulfinilo, haloalquilsulfinilo, alquilsulfonilo o haloalquilsulfonilo; R5 es halogeno, alquilo, haloalquilo, hidroxilo, alcoxi, alcoxialquilo, alcoxialcoxi, cicloalquilo, alqueniloxi, alquiniloxi, benciloxi, cicloalquilalcoxi, haloalcoxi, haloalcoxialquilo, -SH, alquilsulfanilo, haloalquilsulfanilo, alquilsulfinilo, haloalquilsulfinilo, alquilsulfonilo, haloalquilsulfonilo, ciano, nitro, alquilcarbonilo, alcoxicarbonilo, alcoxicarbonilalquilo, carboxilo, carboxamida, dialquilcarboxamida, trialquilsililo, nitro, amino, alquilamino, dialquilamino, alquilsulfonilamino, dialquilsulfonilamino, formilo, -CH=NO-H, -CH=NO-alquilo, -CH=NO-haloalquilo, -C(CH3)=NO-H, -C(CH3)NO-alquilo, -C(CH3)=NO-haloalquilo o heteroarilo, donde el anillo heteroaromático puede estar opcionalmente mono o polisustituido con uno o más sustituyentes seleccionados independientemente entre halogeno, alquilo, haloalquilo y alcoxi; y los N-oxidos y sales dejos compuestos de formula general (1).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09161568A EP2266973A1 (de) | 2009-05-29 | 2009-05-29 | Pyrazinylpyrazole |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR076798A1 true AR076798A1 (es) | 2011-07-06 |
Family
ID=40897591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100101827A AR076798A1 (es) | 2009-05-29 | 2010-05-26 | Pirazinilpirazoles y composiciones que comprenden dichos compuestos |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US20120190687A1 (es) |
| EP (2) | EP2266973A1 (es) |
| KR (1) | KR101758935B1 (es) |
| CN (1) | CN102459235B (es) |
| AR (1) | AR076798A1 (es) |
| AU (1) | AU2010252346B2 (es) |
| BR (1) | BRPI1012771A2 (es) |
| CA (1) | CA2763498A1 (es) |
| CO (1) | CO6470821A2 (es) |
| DO (1) | DOP2011000366A (es) |
| EC (1) | ECSP11011487A (es) |
| ES (1) | ES2409891T3 (es) |
| IL (1) | IL216337A (es) |
| MX (1) | MX2011012504A (es) |
| NI (1) | NI201100208A (es) |
| NZ (1) | NZ596681A (es) |
| PE (1) | PE20120320A1 (es) |
| TW (1) | TW201107310A (es) |
| UY (1) | UY32659A (es) |
| WO (1) | WO2010136145A1 (es) |
| ZA (1) | ZA201108637B (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2533798T3 (es) | 2009-10-12 | 2015-04-14 | Bayer Cropscience Ag | 1-(pirid-3-il)-pirazol y 1-(pirimid-5-il)- pirazol como agentes para combatir parásitos |
| AR078576A1 (es) * | 2009-10-12 | 2011-11-16 | Bayer Cropscience Ag | Amidas y tioamidas de diazol utiles para combatir parasitos animales, en particular insectos y procedimiento para prepararlas. |
| AR078947A1 (es) | 2009-11-11 | 2011-12-14 | Bayer Cropscience Ag | Compuestos de diazinil-pirazolilo y procesos de preparacion de los mismos |
| CA2803695A1 (en) | 2010-06-28 | 2012-01-05 | Bayer Intellectual Property Gmbh | Heteroaryl-substituted pyridine compounds for use as pesticides |
| DE102010063691A1 (de) * | 2010-12-21 | 2012-06-21 | Bayer Animal Health Gmbh | Ektoparasitizide Wirkstoffkombinationen |
| AU2012342564A1 (en) | 2011-11-21 | 2014-06-12 | Basf Se | Process for preparing N-substituted 1H-pyrazole-5-carboxylate compounds and derivatives thereof |
| KR20150050527A (ko) | 2012-05-04 | 2015-05-08 | 바스프 에스이 | 치환된 피라졸-함유 화합물 및 이의 살충제로서의 용도 |
| BR112015007578B1 (pt) * | 2012-10-02 | 2020-05-05 | Bayer Cropscience Ag | Uso não terapêutico de compostos, compostos, composições emétodo não terapêutico para controlar pragas compreendendoos referidos compostos |
| BR112015009751A2 (pt) * | 2012-10-31 | 2017-07-11 | Bayer Cropscience Ag | novos compostos heterocíclicos como pesticidas |
| WO2016174049A1 (en) * | 2015-04-30 | 2016-11-03 | Bayer Animal Health Gmbh | Anti-parasitic combinations including halogen-substituted compounds |
| CN107635967B (zh) | 2015-06-18 | 2021-03-26 | 日本曹达株式会社 | 二芳基唑化合物和有害生物防除剂 |
| WO2017094790A1 (ja) * | 2015-11-30 | 2017-06-08 | 北興化学工業株式会社 | １，２，３－トリアゾール誘導体および当該誘導体を有効成分とする殺虫・殺ダニ剤 |
| EP3872068A1 (en) | 2015-12-16 | 2021-09-01 | Nippon Soda Co., Ltd. | Arylazole compound and pest control agent |
| US11078181B2 (en) | 2016-12-19 | 2021-08-03 | Nippon Soda Co., Ltd. | Diaryl pyrazole compound and formulation for controlling harmful organisms |
| CN110305115A (zh) * | 2019-08-19 | 2019-10-08 | 南通大学 | 一种含1-(6-氯吡嗪-2-基)-3-甲氧基吡唑单元的吡唑肟衍生物的制备和应用 |
| CA3181349A1 (en) * | 2020-04-29 | 2021-11-04 | Bayer Aktiengesellschaft | 1-pyrazinylpyrazolyl-3-oxyalkyl acids and their derivatives, and their use for control of undesired plant growth |
| WO2024121264A1 (en) | 2022-12-09 | 2024-06-13 | Syngenta Crop Protection Ag | Insecticidal compound based on pyrazole derivatives |
| WO2024121262A1 (en) | 2022-12-09 | 2024-06-13 | Syngenta Crop Protection Ag | Insecticidal compound based on pyrazole derivatives |
| WO2024121261A1 (en) | 2022-12-09 | 2024-06-13 | Syngenta Crop Protection Ag | Insecticidal compound based on pyrazole derivatives |
| WO2024121263A1 (en) | 2022-12-09 | 2024-06-13 | Syngenta Crop Protection Ag | Insecticidal compound based on pyrazole derivatives |
| CN120136787A (zh) * | 2023-12-13 | 2025-06-13 | 青岛清原化合物有限公司 | 一种吡唑取代的芳基硫化物类化合物及其应用 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL253320A (es) | 1959-07-03 | |||
| US4101540A (en) | 1975-09-30 | 1978-07-18 | Produits Chimiques Ugine Kuhlmann | 3-Trifluoromethyl-4-phenyl-pyrazolium azo dyestuffs |
| FR2326421A1 (fr) | 1975-09-30 | 1977-04-29 | Ugine Kuhlmann | Nouveaux trifluoromethyl-3-aryl-4 amino-5 pyrazoles et leur application comme bases diazotables pour la synthese de matieres colorantes |
| JPH08208620A (ja) | 1995-02-03 | 1996-08-13 | Takeda Chem Ind Ltd | アミノピラゾール誘導体、その製造法および用途 |
| DE19544799A1 (de) * | 1995-12-01 | 1997-06-05 | Bayer Ag | Substituierte 5-Aminopyrazole |
| CN1105707C (zh) | 1997-01-27 | 2003-04-16 | 第一制药株式会社 | 吡唑衍生物 |
| US6169086B1 (en) | 1997-01-27 | 2001-01-02 | Daiichi Pharmaceutical Co., Ltd. | Pyrazole derivatives |
| CA2297780A1 (en) | 1998-06-10 | 1999-12-16 | Boulder Scientific Company | Synthesis of aryl boronic acids |
| WO2001007413A1 (en) * | 1999-07-22 | 2001-02-01 | 3-Dimensional Pharmaceuticals, Inc. | 1-aryl-3-thioalkyl pyrazoles, the synthesis thereof and the use thereof as insecticides |
| US7514464B2 (en) | 2003-12-18 | 2009-04-07 | Pfizer Limited | Substituted arylpyrazoles |
| WO2007027842A1 (en) | 2005-08-31 | 2007-03-08 | Bayer Healthcare Llc | Anilinopyrazole derivatives useful for the treatment of diabetes |
| WO2007048733A1 (de) | 2005-10-28 | 2007-05-03 | Basf Se | Verwendung von 5-amino-pyrazolen zur bekämpfung pflanzenpathogener schadpilze, neue 5-amino-pyrazole, verfahren zu ihrer herstellung und sie enthaltende mittel |
| DE102007003036A1 (de) | 2006-12-20 | 2008-06-26 | Bayer Cropscience Ag | Pyrimidinylpyrazole |
| WO2009156090A2 (de) * | 2008-06-26 | 2009-12-30 | Bayer Cropscience Aktiengesellschaft | Insektizide schwefel-derivatisierte 1-azinylpyrazole |
| AR078947A1 (es) * | 2009-11-11 | 2011-12-14 | Bayer Cropscience Ag | Compuestos de diazinil-pirazolilo y procesos de preparacion de los mismos |
-
2009
- 2009-05-29 EP EP09161568A patent/EP2266973A1/de not_active Withdrawn
-
2010
- 2010-05-19 ES ES10721330T patent/ES2409891T3/es active Active
- 2010-05-19 CA CA2763498A patent/CA2763498A1/en not_active Abandoned
- 2010-05-19 WO PCT/EP2010/003060 patent/WO2010136145A1/de not_active Ceased
- 2010-05-19 US US13/375,164 patent/US20120190687A1/en not_active Abandoned
- 2010-05-19 NZ NZ596681A patent/NZ596681A/en not_active IP Right Cessation
- 2010-05-19 AU AU2010252346A patent/AU2010252346B2/en not_active Ceased
- 2010-05-19 CN CN201080033587.6A patent/CN102459235B/zh not_active Expired - Fee Related
- 2010-05-19 MX MX2011012504A patent/MX2011012504A/es active IP Right Grant
- 2010-05-19 EP EP10721330A patent/EP2435420B1/de not_active Not-in-force
- 2010-05-19 BR BRPI1012771A patent/BRPI1012771A2/pt not_active Application Discontinuation
- 2010-05-19 PE PE2011002013A patent/PE20120320A1/es not_active Application Discontinuation
- 2010-05-19 KR KR1020117031386A patent/KR101758935B1/ko not_active Expired - Fee Related
- 2010-05-25 UY UY0001032659A patent/UY32659A/es not_active Application Discontinuation
- 2010-05-26 AR ARP100101827A patent/AR076798A1/es unknown
- 2010-05-28 TW TW099117101A patent/TW201107310A/zh unknown
- 2010-05-28 US US12/801,253 patent/US8513260B2/en not_active Expired - Fee Related
-
2011
- 2011-11-14 IL IL216337A patent/IL216337A/en not_active IP Right Cessation
- 2011-11-24 ZA ZA2011/08637A patent/ZA201108637B/en unknown
- 2011-11-24 CO CO11161605A patent/CO6470821A2/es not_active Application Discontinuation
- 2011-11-25 DO DO2011000366A patent/DOP2011000366A/es unknown
- 2011-11-28 EC EC2011011487A patent/ECSP11011487A/es unknown
- 2011-11-28 NI NI201100208A patent/NI201100208A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| UY32659A (es) | 2010-12-31 |
| BRPI1012771A2 (pt) | 2016-03-29 |
| DOP2011000366A (es) | 2011-12-15 |
| NI201100208A (es) | 2012-08-17 |
| WO2010136145A1 (de) | 2010-12-02 |
| KR101758935B1 (ko) | 2017-07-17 |
| EP2435420A1 (de) | 2012-04-04 |
| TW201107310A (en) | 2011-03-01 |
| CN102459235B (zh) | 2015-03-11 |
| IL216337A (en) | 2015-09-24 |
| NZ596681A (en) | 2015-09-25 |
| ZA201108637B (en) | 2013-01-30 |
| IL216337A0 (en) | 2012-01-31 |
| CO6470821A2 (es) | 2012-06-29 |
| PE20120320A1 (es) | 2012-03-30 |
| MX2011012504A (es) | 2011-12-12 |
| US20110021539A1 (en) | 2011-01-27 |
| EP2435420B1 (de) | 2013-04-03 |
| CN102459235A (zh) | 2012-05-16 |
| KR20120061779A (ko) | 2012-06-13 |
| EP2266973A1 (de) | 2010-12-29 |
| AU2010252346A1 (en) | 2011-12-22 |
| CA2763498A1 (en) | 2010-12-02 |
| ES2409891T3 (es) | 2013-06-28 |
| US8513260B2 (en) | 2013-08-20 |
| ECSP11011487A (es) | 2011-12-30 |
| US20120190687A1 (en) | 2012-07-26 |
| AU2010252346B2 (en) | 2015-11-19 |
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