AR070680A1 - Derivados herbicidas de piridazinona - Google Patents

Derivados herbicidas de piridazinona

Info

Publication number
AR070680A1
AR070680A1 ARP080105555A ARP080105555A AR070680A1 AR 070680 A1 AR070680 A1 AR 070680A1 AR P080105555 A ARP080105555 A AR P080105555A AR P080105555 A ARP080105555 A AR P080105555A AR 070680 A1 AR070680 A1 AR 070680A1
Authority
AR
Argentina
Prior art keywords
alkyl
independently
ring
cycloalkyl
alkylaminocarbonyl
Prior art date
Application number
ARP080105555A
Other languages
English (en)
Inventor
Andrew E Taggi
Thomas Martin Stevenson
Eric Allen Marshall
Original Assignee
Du Pont
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Du Pont filed Critical Du Pont
Publication of AR070680A1 publication Critical patent/AR070680A1/es

Links

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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/14—Oxygen atoms
    • C07D237/16—Two oxygen atoms
    • 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
    • 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
    • C07D403/10—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 linked by a carbon chain containing aromatic 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
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D417/04—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 directly linked by a ring-member-to-ring-member bond
    • 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

Abstract

También se describen composiciones que contienen los compuestos de formula (1) y métodos para controlar la vegetacion indeseable que comprenden poner en contacto la vegetacion indeseable o su ambiente con una cantidad eficaz de un compuesto o una composicion de la presente. Reivindicacion 1: Un compuesto caracterizado porque se selecciona entre la formula (1), sus N-oxidos y sales, donde R1 es H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, cicloalquilcicloalquilo C6-14, halocicloalquilalquilo C4-10, alquilcicloalquilalquilo C5-12, cicloalquenilo C3-8, halocicloalquenilo C3-8, alcoxialquilo C2-8, cicloalcoxialquilo C4-10, alcoxialcoxialquilo C3-10, alquiltioalquilo C2-8, alquilsulfinilalquilo C2-8, alquilsulfonilalquilo C2-8, tetrahidropiranilo, -C(=W6)R4, -C(=W2)W3R5, -S(=O)2R6, -P(=W4)R7R8 o -C(=W5)NR9R10; R2 es H, halogeno, ciano, -C(=O)OH, -C(=O)NH2, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, cicloalquilcicloalquilo C6-14, halocicloalquilalquilo C4-10, alquilcicloalquilalquilo C5-12, cicloalquenilo C3-8, halocicloalquenilo C3-8, alcoxialquilo C2-8, cicloalcoxialquilo C4-10, alcoxialcoxialquilo C3-10, alquiltioalquilo C2-8, alquilsulfinilalquilo C2-8, alquilsulfonilalquilo C2-8, alcoxicarbonilo C2-8, cicloalcoxicarbonilo C4-10, cicloalquilalcoxicarbonilo C5-12, alquilaminocarbonilo C2-8, dialquilaminocarbonilo C3-10, cicloalquilaminocarbonilo C4-10, alcoxi C1-6, haloalcoxi C1-6, alquiltio C1-6, haloalquiltio C1-6, nitro, cicloalcoxi C3-6 o cicloalquilalcoxi C4-8; R3 es H, -C(=W6)R4, -C(=W2)W3R5, -S(=O)2R6, -P(=W4)R7R8 o -C(=W5)NR9R10; G es un anillo fenilo o un anillo heteroaromático de 5 o 6 miembros, cada anillo se sustituye opcionalmente con RX sobre los nitrogenos miembros del anillo y se sustituye opcionalmente con hasta 4 sustituyentes seleccionados entre RW sobre carbonos miembros del anillo; J es un anillo fenilo o un anillo heteroaromático de 5 o 6 miembros, cada anillo se sustituye opcionalmente con hasta 5 sustituyentes seleccionados en forma independiente entre RU; cada R4 es en forma independiente alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, alquilcicloalquilalquilo C5-12, cicloalquenilo C3-8, alcoxialquilo C2-8, cicloalcoxialquilo C4-10, alcoxialcoxialquilo C3-10, alquiltioalquilo C2-8, alquilsulfinilalquilo C2-8, alquilsulfonilalquilo C2-8, alquilaminoalquilo C2-8, dialquilaminoalquilo C3-10, haloalquilaminoalquilo C2-8, o cicloalquilaminoalquilo C4-10, naftalenilo o -(CR11R12)nGA; cada R5 es en forma independiente alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, alquilcicloalquilalquilo C5-12, cicloalquenilo C3-10, alcoxialquilo C2-8, cicloalcoxialquilo C4-10, alcoxialcoxialquilo C3-10, alquiltioalquilo C2-8, alquilsulfinilalquilo C2-8, alquilsulfonilalquilo C2-8, alquilaminoalquilo C2-8, dialquilaminoalquilo C3-10, haloalquilaminoalquilo C2-8, cicloalquilaminoalquilo C4-10, naftalenilo o -(CR11R12)nGA; cada R6 es en forma independiente alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, halocicloalquilo C4-10, alquilcicloalquilalquilo C5-12, cicloalquenilo C3-8, alcoxialquilo C2-8, cicloalcoxialquilo C4-10, alcoxialcoxialquilo C3-10, alquiltioalquilo C2-8, alquilsulfinilalquilo C2-8, alquilsulfonilalquilo C2-8, alquilaminoalquilo C2-8, dialquilaminoalquilo C3-10, haloalquilaminoalquilo C2-8, cicloalquilaminoalquilo C4-10, alquilamino C1-6, dialquilamino C2-8, haloalquilamino C2-6, halodialquilamino C2-8, cicloalquilamino C3-8, alquilcarbonilamino C2-8, haloalquilcarbonilamino C2-8, alquilsulfonilamino C1-6, haloalquilsulfonilamino C1-6, naftalenilo o -(CR11R12)nGA; cada R7 y R8 es en forma independiente alquilo C1-6, alcoxi C1-6, alquilamino C1-6, dialquilamino C2-8, haloalquilamino C2-6, halodialquilamino C2-8, cicloalquilamino C3-8, naftalenilo o -(CR11R12)nGA; cada R9 es en forma independiente H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, alquilcicloalquilalquilo C5-12, cicloalquenilo C3-8, alcoxialquilo C2-8, cicloalcoxialquilo C4-10, alcoxialcoxialquilo C3-10, alquiltioalquilo C2-8, alquilsulfinilalquilo C2-8, alquilsulfonilalquilo C2-8, alquilaminoalquilo C2-8, dialquilaminoalquilo C4-10, naftalenilo o -(CR11R12)nGA; cada R10 es en forma independiente H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, haloalquenilo C2-6, haloalquinilo C2-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, o cicloalquilalquilo C4-10, o R9 y R10 se toman juntos con el nitrogeno al cual se encuentran unidos para formar un anillo heterocíclico de 3 a 7 miembros que contiene, además del nitrogeno de la union, miembros del anillo seleccionados entre carbono y opcionalmente O, S y NR13, los carbonos miembros del anillo opcionalmente en forma de C(=O), y el anillo opcionalmente sustituido sobre carbonos miembros del anillo con hasta 4 sustituyentes en forma independiente seleccionados entre el grupo que consiste en halogeno, -CN, alquilo C1-3 y alcoxi C1-3; cada R11 y R12 es en forma independiente H o alquilo C1-3; cada R13 es en forma independiente H o alquilo C1-3; cada GA es en forma independiente un anillo fenilo o un anillo heteroaromático de 5 o 6 miembros, cada anillo se sustituye opcionalmente con hasta 5 sustituyentes seleccionados en forma independiente entre RU, o un sistema de anillos naftaleno opcionalmente sustituido con hasta 5 sustituyentes seleccionados en forma independiente entre RU; cada RU es en forma independiente halogeno, ciano, hidroxi, amino, nitro, -CHO, -C(=O)OH, -C(=O)NH2, -SO2NH2, SF5, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, halocicloalquilalquilo C4-10, alquilcicloalquilalquilo C5-12, alquilcarbonilo C2-8, haloalquilcarbonilo C2-8, alcoxicarbonilo C2-8, cicloalcoxicarbonilo C4-10, cicloalquilalcoxicarbonilo C5-12, alquilaminocarbonilo C2-8, dialquilaminocarbonilo C3-10, alcoxi C1-6, haloalcoxi C1-6, alquilcarboniloxi C2-8, alquiltio C1-6, haloalquiltio C1-6, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, alquilaminosulfonilo C1-6, dialquilaminosulfonilo C2-8, trialquilsililo C3-10, alquilamino C1-6, dialquilamino C2-8, alquilaminocarbonilo C2-8, alquilsulfonilamino C1-6, fenilo, piridinilo o tienilo; cada RW es en forma independiente halogeno; ciano, hidroxi, amino, nitro, -CHO, -C(=O)OH, -C(=O)NH2, -SO2NH2, SF5, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6, cicloalquilo C3-8, halocicloalquilo C3-8, alquilcicloalquilo C4-10, cicloalquilalquilo C4-10, halocicloalquilalquilo C4-10, alquilcicloalquilalquilo C5-12, alquilcarbonilo C2-8, haloalquilcarbonilo C2-8, alcoxicarbonilo C2-8, cicloalcoxicarbonilo C4-10, cicloalquilalcoxicarbonilo C5-12, alquilaminocarbonilo C2-8, dialquilaminocarbonilo C3-10, alcoxi C1-6, haloalcoxi C1-6, alquilcarboniloxi C2-8, alquiltio C1-6, haloalquiltio C1-6, alquilsulfinilo C1-6, haloalquilsulfinilo C1-6, alquilsulfonilo C1-6, haloalquilsulfonilo C1-6, alquilaminosulfonilo C1-6, dialquilaminosulfonilo C2-8, trialquilsililo C3-10, alquilamino C1-6, dialquilamino C2-8, alquilaminocarbonilo C2-8, alquilsulfonilamino C1-6, naftalenilo, -O(CR11R12)nGA o -(CR11R12)nGA; cada RX es en forma independiente H, alquilo C1-3 o cicloalquilo C3-7; cada W1, W2, W3, W4, W5 y W6 es en forma independiente O o S; y cada n es en forma independiente un entero seleccionado de entre 0 y 3.
ARP080105555A 2007-12-21 2008-12-19 Derivados herbicidas de piridazinona AR070680A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US886107P 2007-12-21 2007-12-21

Publications (1)

Publication Number Publication Date
AR070680A1 true AR070680A1 (es) 2010-04-28

Family

ID=40456320

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080105555A AR070680A1 (es) 2007-12-21 2008-12-19 Derivados herbicidas de piridazinona

Country Status (18)

Country Link
US (1) US20100267561A1 (es)
EP (1) EP2225211B1 (es)
JP (1) JP2011507893A (es)
KR (1) KR20100099735A (es)
CN (1) CN101945856A (es)
AR (1) AR070680A1 (es)
AU (1) AU2008343031A1 (es)
BR (1) BRPI0819528A2 (es)
CA (1) CA2707520A1 (es)
CL (1) CL2008003785A1 (es)
CO (1) CO6280580A2 (es)
IL (1) IL206131A0 (es)
MY (1) MY150588A (es)
NZ (1) NZ585728A (es)
RU (1) RU2010130559A (es)
UA (1) UA99494C2 (es)
UY (1) UY31553A1 (es)
WO (1) WO2009086041A1 (es)

Families Citing this family (83)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7344702B2 (en) 2004-02-13 2008-03-18 Bristol-Myers Squibb Pharma Company Contrast agents for myocardial perfusion imaging
US20080200431A1 (en) * 2005-07-08 2008-08-21 Astrazeneca Ab Heterocyclic Sulfonamide Derivatives as Inhibitors of Factor Xa
DE102007026341A1 (de) 2007-06-06 2008-12-11 Merck Patent Gmbh Benzoxazolonderivate
GB0712653D0 (en) * 2007-06-28 2007-08-08 Syngenta Ltd Novel herbicides
DE102007032507A1 (de) 2007-07-12 2009-04-02 Merck Patent Gmbh Pyridazinonderivate
GB0714981D0 (en) 2007-08-01 2007-09-12 Syngenta Ltd Novel herbicides
US8097712B2 (en) 2007-11-07 2012-01-17 Beelogics Inc. Compositions for conferring tolerance to viral disease in social insects, and the use thereof
DE102007061963A1 (de) 2007-12-21 2009-06-25 Merck Patent Gmbh Pyridazinonderivate
DK2257315T3 (da) 2008-02-29 2020-01-27 Lantheus Medical Imaging Inc Kontrastmidler til anvendelser omfattende perfusionsbilleddannelse
DE102008019907A1 (de) 2008-04-21 2009-10-22 Merck Patent Gmbh Pyridazinonderivate
DE102008028905A1 (de) 2008-06-18 2009-12-24 Merck Patent Gmbh 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate
EP2204366A1 (de) * 2008-12-19 2010-07-07 Bayer CropScience AG Herbizid und insektizid wirksame phenylsubstituierte Pyridazinone
US8586599B2 (en) 2008-12-22 2013-11-19 Merck Patent Gmbh Polymorphic forms of 6-(1-methyl-1H-pyrazol-4-yl)-2-{3-[5-(2-morpholin-4-yl-ethoxy)-pyrimidin-2-yl]-benzyl}-2H-pyridazin-3-one dihydrogenphosphate and processes of manufacturing thereof
JP2010235591A (ja) * 2009-03-13 2010-10-21 Sumitomo Chemical Co Ltd 除草用組成物
US20120028988A1 (en) * 2009-03-30 2012-02-02 Sumitomo Chemical Company, Limited Use of pyridazinone compound for control of harmful arthropod pests
US20100267706A1 (en) * 2009-04-20 2010-10-21 Institute For Oneworld Health Compounds, Compositions and Methods Comprising Pyridazine Derivatives
JP5795581B2 (ja) 2009-07-31 2015-10-14 シンジェンタ リミテッド 除草活性を有するヘテロアリール置換環状ジオンまたはその誘導体
WO2011035878A1 (de) * 2009-09-25 2011-03-31 Bayer Cropscience Ag Herbizid wirksame phenylsubstituierte pyridazinone
GB201117019D0 (en) * 2011-10-04 2011-11-16 Syngenta Ltd Herbicidal compounds
EP2308866A1 (de) * 2009-10-09 2011-04-13 Bayer CropScience AG Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide
US8962584B2 (en) 2009-10-14 2015-02-24 Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. Compositions for controlling Varroa mites in bees
WO2011045271A1 (de) 2009-10-15 2011-04-21 Bayer Cropscience Ag Herbizid wirksame heterocyclylsubstituierte pyridazinone
CN109200296B (zh) 2010-02-08 2021-12-14 兰休斯医疗成像公司 用于合成显像剂和其中间体的方法和装置
US9121022B2 (en) 2010-03-08 2015-09-01 Monsanto Technology Llc Method for controlling herbicide-resistant plants
EP2614053B1 (en) 2010-09-08 2016-03-23 Sumitomo Chemical Company Limited Method for producing pyridazinone compounds and intermediates thereof
JP5842594B2 (ja) * 2010-12-27 2016-01-13 住友化学株式会社 ピリダジノン化合物、それを含有する除草剤及び有害節足動物防除剤
AU2012308659B2 (en) 2011-09-13 2017-05-04 Monsanto Technology Llc Methods and compositions for weed control
US10806146B2 (en) 2011-09-13 2020-10-20 Monsanto Technology Llc Methods and compositions for weed control
UA116090C2 (uk) 2011-09-13 2018-02-12 Монсанто Текнолоджи Ллс Спосіб та композиція для боротьби з бур'янами (варіанти)
US10760086B2 (en) 2011-09-13 2020-09-01 Monsanto Technology Llc Methods and compositions for weed control
AU2012308694B2 (en) 2011-09-13 2018-06-14 Monsanto Technology Llc Methods and compositions for weed control
AU2012308686B2 (en) 2011-09-13 2018-05-10 Monsanto Technology Llc Methods and compositions for weed control
US10829828B2 (en) 2011-09-13 2020-11-10 Monsanto Technology Llc Methods and compositions for weed control
CN103975068A (zh) 2011-09-13 2014-08-06 孟山都技术公司 用于杂草控制的方法和组合物
WO2013040021A1 (en) 2011-09-13 2013-03-21 Monsanto Technology Llc Methods and compositions for weed control
MX348495B (es) 2011-09-13 2017-06-14 Monsanto Technology Llc Metodos y composiciones para el control de malezas.
GB201206598D0 (en) * 2012-04-13 2012-05-30 Syngenta Ltd Herbicidal compounds
AR091143A1 (es) 2012-05-24 2015-01-14 Seeds Ltd Ab Composiciones y metodos para silenciar la expresion genetica
AU2013203000B9 (en) * 2012-08-10 2017-02-02 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
WO2014031971A1 (en) * 2012-08-24 2014-02-27 E. I. Du Pont De Nemours And Company Herbicidal pyridazinones
US10683505B2 (en) 2013-01-01 2020-06-16 Monsanto Technology Llc Methods of introducing dsRNA to plant seeds for modulating gene expression
BR112015015975A2 (pt) 2013-01-01 2018-11-06 A. B. Seeds Ltd. moléculas de dsrna isoladas e métodos de uso das mesmas para silenciamento das moléculas alvo de interesse.
WO2014119770A1 (ja) * 2013-01-30 2014-08-07 住友化学株式会社 ピリダジノン化合物及びそれを含有する除草剤
UY35385A (es) 2013-03-13 2014-09-30 Monsanto Technology Llc ?métodos y composiciones para el control de malezas?.
AU2014249015B2 (en) 2013-03-13 2020-04-16 Monsanto Technology Llc Methods and compositions for weed control
US10568328B2 (en) 2013-03-15 2020-02-25 Monsanto Technology Llc Methods and compositions for weed control
RU2703498C2 (ru) 2013-07-19 2019-10-17 Монсанто Текнолоджи Ллс Композиции и способы борьбы с leptinotarsa
US9850496B2 (en) 2013-07-19 2017-12-26 Monsanto Technology Llc Compositions and methods for controlling Leptinotarsa
GB201317791D0 (en) * 2013-10-08 2013-11-20 Syngenta Ltd Herbicidal compounds
GB2519092A (en) * 2013-10-08 2015-04-15 Syngenta Ltd Herbicidal Compounds
AU2014341879B2 (en) 2013-11-04 2020-07-23 Beeologics, Inc. Compositions and methods for controlling arthropod parasite and pest infestations
WO2015084936A1 (en) * 2013-12-04 2015-06-11 The Scripps Research Institute Novel compounds as jnk kinase inhibitors
UA119253C2 (uk) 2013-12-10 2019-05-27 Біолоджикс, Інк. Спосіб боротьби із вірусом у кліща varroa та у бджіл
AU2015206585A1 (en) 2014-01-15 2016-07-21 Monsanto Technology Llc Methods and compositions for weed control using EPSPS polynucleotides
WO2015153339A2 (en) 2014-04-01 2015-10-08 Monsanto Technology Llc Compositions and methods for controlling insect pests
PT3137456T (pt) 2014-04-29 2021-08-06 Fmc Corp Herbicidas de piridazinona
AU2015280252A1 (en) 2014-06-23 2017-01-12 Monsanto Technology Llc Compositions and methods for regulating gene expression via RNA interference
US11807857B2 (en) 2014-06-25 2023-11-07 Monsanto Technology Llc Methods and compositions for delivering nucleic acids to plant cells and regulating gene expression
GB201412735D0 (en) * 2014-07-17 2014-09-03 Syngenta Participations Ag Herbicidal compounds
RU2021123470A (ru) 2014-07-29 2021-09-06 Монсанто Текнолоджи Ллс Композиции и способы борьбы с насекомыми-вредителями
US10202361B2 (en) 2014-08-29 2019-02-12 Fmc Corporation Pyridazinones as herbicides
WO2016118762A1 (en) 2015-01-22 2016-07-28 Monsanto Technology Llc Compositions and methods for controlling leptinotarsa
GB201507464D0 (en) 2015-04-30 2015-06-17 Syngenta Participations Ag Herbicidal compounds
UY36703A (es) 2015-06-02 2016-12-30 Monsanto Technology Llc Composiciones y métodos para la administración de un polinucleótido en una planta
WO2016196782A1 (en) 2015-06-03 2016-12-08 Monsanto Technology Llc Methods and compositions for introducing nucleic acids into plants
GB201511631D0 (en) 2015-07-02 2015-08-19 Syngenta Participations Ag Improvements in or relating to organic compounds
EP3368523B1 (en) 2015-10-28 2021-07-14 FMC Corporation Novel pyridazinone herbicides
US10913719B2 (en) 2015-10-28 2021-02-09 Fmc Corporation Intermediates to prepare pyridazinone herbicides, and a process to prepare them
LT3438095T (lt) 2016-03-30 2021-09-10 Ishihara Sangyo Kaisha, Ltd. Piridazinono junginys arba jo druska ir jį turintis herbicidas
TWI785022B (zh) 2017-03-28 2022-12-01 美商富曼西公司 新穎噠嗪酮類除草劑
WO2019005484A1 (en) 2017-06-30 2019-01-03 Fmc Corporation 4- (3,4-DIHYDRONAPHTH-1-YL OR 2H-CHROMEN-4-YL) -5-HYDROXY-2H-PYRADIZIN-3-ONES AS HERBICIDES
JP2021008405A (ja) * 2017-09-27 2021-01-28 石原産業株式会社 ピリダジノン系化合物又はその塩、及びそれらを含有する除草剤
GB201800305D0 (en) 2018-01-09 2018-02-21 Syngenta Participations Ag Herbicidal compounds
US20210045385A1 (en) 2018-01-21 2021-02-18 Fmc Corporation Pyridazinone-substituted ketoximes as herbicides
CN108997325B (zh) * 2018-07-06 2020-08-04 浙江工业大学 一种芳基联噻唑类化合物和应用
GB201819747D0 (en) 2018-12-04 2019-01-16 Syngenta Participations Ag Herbicidal compositions
US11700850B2 (en) * 2018-12-05 2023-07-18 Valent U.S.A., Llc Aqueous herbicidal compositions and methods of use thereof
JPWO2020204112A1 (es) * 2019-04-01 2020-10-08
GB201910291D0 (en) 2019-07-18 2019-09-04 Syngenta Crop Protection Ag Herbicidal compounds
GB201910290D0 (en) 2019-07-18 2019-09-04 Syngenta Crop Protection Ag Herbicidal compounds
GB202012651D0 (en) 2020-08-13 2020-09-30 Syngenta Crop Protection Ag Herbicidal compositions
JP2024517155A (ja) 2021-04-27 2024-04-19 バイエル・アクチエンゲゼルシヤフト 置換ピリダジノン、その塩またはｎ－オキシドおよび除草活性物質としてのそれらの使用
WO2023189602A1 (ja) * 2022-03-30 2023-10-05 石原産業株式会社 ピリダジノン系化合物又はその塩及びそれらを含有する有害生物防除剤

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL126015C (es) * 1964-02-12
DE4009761A1 (de) * 1989-07-28 1991-01-31 Bayer Ag 2h-pyridazinon-derivate
US5723411A (en) * 1995-10-31 1998-03-03 E. I. Du Pont De Nemours And Company Herbicidal pyridazinones
JPH11152273A (ja) * 1997-11-19 1999-06-08 Otsuka Chem Co Ltd 窒素含有６員環ジオン誘導体
DE10152005A1 (de) 2001-10-22 2003-04-30 Bayer Cropscience Ag Pyrazolylsubstituierte Heterocyclen
TWI375669B (en) * 2006-03-17 2012-11-01 Sumitomo Chemical Co Pyridazinone compound and use thereof
WO2007127479A2 (en) * 2006-04-28 2007-11-08 Redpoint Bio Corporation Triaryl substituted imidazole derivatives and taste-inhibiting uses thereof
JP4672695B2 (ja) * 2007-03-22 2011-04-20 三菱電機株式会社 制御システム開発支援装置、制御システム開発支援方法およびその方法をコンピュータに実行させるプログラム

Also Published As

Publication number Publication date
CN101945856A (zh) 2011-01-12
UA99494C2 (ru) 2012-08-27
RU2010130559A (ru) 2012-01-27
UY31553A1 (es) 2009-08-03
KR20100099735A (ko) 2010-09-13
MY150588A (en) 2014-01-30
JP2011507893A (ja) 2011-03-10
IL206131A0 (en) 2010-11-30
CO6280580A2 (es) 2011-05-20
AU2008343031A1 (en) 2009-07-09
EP2225211A1 (en) 2010-09-08
BRPI0819528A2 (pt) 2015-05-26
US20100267561A1 (en) 2010-10-21
CL2008003785A1 (es) 2009-10-09
EP2225211B1 (en) 2013-10-02
WO2009086041A1 (en) 2009-07-09
NZ585728A (en) 2011-11-25
CA2707520A1 (en) 2009-07-09

Similar Documents

Publication Publication Date Title
AR070680A1 (es) Derivados herbicidas de piridazinona
AR081139A1 (es) Uracilos herbicidas
AR074411A1 (es) Compuestos heterociclicos fungicidas
AR082869A1 (es) Pirazoles fungicidas
AR098673A1 (es) Herbicidas de pirrolidinona
AR082373A1 (es) Oximas e hidrazonas fungicidas
RU2017123114A (ru) 3-оксо-3-(ариламино)пропионаты, способ их получения и их применение в получении пирролидинонов
AR104420A1 (es) Butirolactonas como herbicidas
AR099122A1 (es) Derivados de pirimidiniloxi benceno como herbicidas
AR104808A1 (es) Amidas cíclicas sustituidas como herbicidas
AR059494A1 (es) Derivados biciclicos de bisamida con actividad pesticida
AR058896A1 (es) Isoxazolinas para controlar plagas de invertebrados
JP2011507893A5 (es)
AR073252A1 (es) Piridinas fungicidas
AR072459A1 (es) DERIVADOS DE DIONAS CICLICAS ACTIVAS COMO HERBICIDAS, PROCESO DE PREPARACIoN Y COMPOSICIONES QUE COMPRENDEN DICHOS COMPUESTOS
SMT201300098B (it) Forme solide di N-(4-(7-azabiciclo[2.2.1]eptan-7-il)-2-(trifluorometil)fenil-4-osso-5-trifluorometil)-1,4-diidrochinolina-3-carbossammide
JP2013530176A5 (es)
AR058358A1 (es) 5- aril isoxalinas para controlar plagas de invertebrados
AR081998A1 (es) Compuestos de isoxazolinas, composicion para el control de parasitos en base al compuesto, metodo de control de parasitos y uso del compuesto para tal fin
AR090098A1 (es) Pirazoles fungicidas
AR086296A1 (es) Derivados de dihidroisoxasol utiles como parasiticidas tanto en animales como en plantas
AR050967A1 (es) Derivados de bencimidazol utiles como moduladores de los receptores androgenicos (sarms)
AR063048A1 (es) Derivados de n-cicloaquil-carboxamida, tiocarboxamida y carboximidamida n-sustituida fungicidas
AR070803A1 (es) Proceso para la preparacion de derivados de acido 2- amino-5- cianobenzoico
HK1169984A1 (en) Diphenyl-pyrazolopyridine compounds, their preparation and their application as modulators of the nuclear receptor not

Legal Events

Date Code Title Description
FA Abandonment or withdrawal