AR058922A1 - Compuestos de piperazina con accion herbicida - Google Patents
Compuestos de piperazina con accion herbicidaInfo
- Publication number
- AR058922A1 AR058922A1 ARP070100044A ARP070100044A AR058922A1 AR 058922 A1 AR058922 A1 AR 058922A1 AR P070100044 A ARP070100044 A AR P070100044A AR P070100044 A ARP070100044 A AR P070100044A AR 058922 A1 AR058922 A1 AR 058922A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- amino
- phenyl
- alkoxy
- alkynyl
- Prior art date
Links
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical class C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 title abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 27
- -1 piperazine compound Chemical class 0.000 abstract 18
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 15
- 229910052739 hydrogen Inorganic materials 0.000 abstract 15
- 239000001257 hydrogen Substances 0.000 abstract 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 13
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 11
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 11
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 11
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 10
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 10
- 150000002431 hydrogen Chemical class 0.000 abstract 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 8
- 125000003282 alkyl amino group Chemical group 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 150000004885 piperazines Chemical class 0.000 abstract 6
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 5
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 5
- 125000004414 alkyl thio group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 4
- 125000001931 aliphatic group Chemical group 0.000 abstract 4
- 125000002947 alkylene group Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 3
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 3
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 239000004009 herbicide Substances 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 125000000033 alkoxyamino group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 2
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 abstract 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000002671 adjuvant Substances 0.000 abstract 1
- 125000005466 alkylenyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 125000006517 heterocyclyl carbonyl group Chemical group 0.000 abstract 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- GYNAVKULVOETAD-UHFFFAOYSA-N n-phenoxyaniline Chemical compound C=1C=CC=CC=1NOC1=CC=CC=C1 GYNAVKULVOETAD-UHFFFAOYSA-N 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- 230000008635 plant growth Effects 0.000 abstract 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-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
- C07D241/18—Oxygen or sulfur 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero 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
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/06—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members
- C07D241/08—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
-
- 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
- C07D403/06—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 only aliphatic carbon atoms
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D413/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Uso de compuestos de piperazina de formula (1) o de las sales aceptables para uso agrícola de compuestos de piperazina de formula (1) como herbicidas. También medios, que además de los adyuvantes usuales para la formulacion de herbicidas, contienen compuestos de piperazina de formula (1) o las sales aceptables para uso agrícola de (1), así como un procedimiento para la preparacion de estos medios. Además determinados compuestos de piperazina de Formula (1), a un procedimiento para combatir el crecimiento indeseado de plantas, en el que se trata las plantas, sus semillas y/o su hábitat con al menos un compuesto de piperazina de formula (1) Reivindicacion 1: Uso de compuestos de piperazina de formula (1) o de las sales aceptables para uso agrícola de compuestos de piperazina de formula (1) como herbicidas, donde las variables en formula (1) presentan los siguientes significados: R1 y R2 significan independientemente entre sí: ciano, alquilo C1-6, cicloalquilo C3-6, alquenilo C3-6, cicloalquenilo C3-6, alquinilo C3-6, cicloalquinilo C3-6, fenilo, fenil-alquilo C1-6, heterociclilo, heterociclil-alquilo C1-6; fenil-[alcoxicarbonil-C1-6]-alquilo C1-6 o fenilheterociclil-alquilo C1-6; o COR21, donde R21 significa hidrogeno, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, cicloalquenilo C3-6, alquinilo C2-6, cicloalquinilo C3-6, hidroxi, alcoxi C1-6, alqueniloxi C3-6, alquiniloxi C3-6, amino, alquilamino C1-6, [di- alquilo (C1-6)]amino, alquenilamino C3-6, alquinilamino C3-6, alquilsulfonilamino C1-6, N-(alquenilo C2-6)-N-(alquil-C1-6)-amino, N(alquinilo C2-6)-N-(alquil-C1-6)-amino, N-(alcoxi C1-6)-N-(alquil-C1-C6)-amino, N-(alquenilo C2-6)-N-(alcoxi-C1-6)-amino, N-(alquinilo C2-6)-N-(alcoxi-C1-6)- amino, fenilo, fenilamino, fenoxi, naftilo o heterociclilo; o NR22R23, donde R22 y R23 independientemente entre sí significan hidrogeno, alquilo C1-6, cicloalquilo C3-6, alquenilo C3-6, cicloalquenilo C3-6, alquinilo C3-6, cicloalquinilo C3-6 o alquilcarbonilo C1-6; o OR24, donde R24 significa alquilo, C1-6, cicloalquilo C3-6, alquenilo C3-6, cicloalquenilo C3-6, alquinilo C3-6, cicloalquinilo C3-6, fenilo o fenilalquilo C1-6); o SO2R25, donde R25 es alquilo C1-6 o fenilo; donde las partes alifáticas, cíclicas o aromáticas mencionadas de los sustituyentes de R1 y R2 pueden estar halogenadas en forma parcial o total y/o pueden portar uno a tres de los siguientes grupos: ciano, hidroxi, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, alcoxi C1-4, alquiltio C1-4, [di-alquil-(C1- 4)]-amino, alquilcarbonilo C1-4, hidroxicarbonilo, alcoxicarbonilo C1-4, aminocarbonilo, alquilaminocarbonilo C1-4, [di-alquil-(C1-4)]aminocarbonilo o alquilcarboniloxi C1-4; y donde R1 puede además ser hidrogeno; R3 es hidrogeno, halogeno, ciano, alquilo C1x-6x, cicloalquilo C3-6, alquenilo C2-6, cicloalquenilo C3-6, alquinilo C2-6, cicloalquinilo C3-6, fenilo, fenilalquilo C1-6, heterociclilo, heterociclil-alquilo (C1-6); fenil-[alcoxicarbonil-C1- 6]-alquilo C1-6 o fenilheterociclil-alquilo C1-6; o un resto COR26, NR27R28, OR29, SO2R30 o N(OR31)R32, wobei, R26 significa hidrogeno, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, cicloalquenilo C3-6, alquinilo C2-6, cicloalquinilo C3-6, hidroxi, alcoxi C1-6, alqueniloxi C3-6, alquiniloxi C3-6, amino, alquilamino C1-6, [di- alquilo (C1-6)]amino, alcoxiamino C1-6, [di-(C1-6)-alcoxi]amino, alquilsulfonilamino C1-6, alquilamino C1-6sulfonilamino, [di-alquilamino (C1-6)]sulfonilamino, alquenilamino C3-6, alquinilamino C3-6, N-(alquenilo C2-6)-N-(alquil-C1-6)-amino, N-(alquinilo C2-6)-N- (alquil-C1-6)-amino, N(alcoxi C1-6)-N-(alquil-C1-6)-amino, N(alquenilo C2-6)-N-(alcoxi-C1-6)-amino, N-(alquinil C2-6)-N-(alcoxi-C1- 6)-amino, fenilo, fenoxi, fenilamino, naftilo o heterociclilo; o R27 y R28 significan independientemente entre sí hidrogeno, alquilo C1-6, arilo o heteroarilo; R29 significa alquilo C1-6, R30 significa alquilo C1-6 o fenilo; R31 significa hidrogeno, alquilo C1-6, fenilo o fenil-alquilo (C1-6); R32 significa alquilo C1-6, fenilo o fenil-alquilo (C1-6); donde las partes alifáticas, cíclicas o aromáticas mencionadas de los sustituyentes de R3 o bien R26, R27, R28, R29, R30, R31 y R32 pueden estar halogenadas en forma parcial .o total y/o pueden portar uno a tres de los siguientes grupos: ciano, hidroxi, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, alcoxi C1-4, alquiltio C1-4, [di-alquil-(C1-4)]-amino, alquilcarbonilo C1-4, hidroxicarbonilo; alcoxicarbonilo C1-4, aminocarbonilo, alquilaminocarbonilo C1-4, [di-alquil-(C1-4]aminocarbonilo o alquilcarboniloxi C1-4; R4, R5, R6 independientemente entre sí pueden ser hidrogeno, hidroxi, alquilo C1x-6x, alcoxi C1-C6, donde las partes alifáticas mencionadas de los sustituyentes de R4, R5 o R6 pueden estar halogenadas en forma parcial o total y/o pueden portar uno a tres de los siguientes grupos: ciano, hidroxi, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, alcoxi C1-4, alquiltio C1-4, [di-alquil-(C1- 4)]-amino, alquilcarbonilo C1-4, hidroxicarbonilo, alcoxicarbonilo C1-4, aminocarbonilo, alquilaminocarbonilo C1-4, [di-alquil-(C1-4)]aminocarbonilo o alquilcarboniloxi C1-4; A1 es arilo o heteroarilo; A2 es arilo o heteroarilo, salvo indolilo; Ra es halogeno, ciano, nitro, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, cicloalquenilo C3-6, alcandienilo C4-10, alquinilo C2-6, [Tri-alquil-(C1-6)-silil]-alquinilo (C2-6), cicloalquinilo C3-6, alquiltio C1-6, alquilsulfinilo C1-6, arilo, fenil-alquilo (C1-6), fenil-alquenilo-(C2-6), fenilsulfonil-alquilo (C1-6), heterociclilo, heterociclil-alquilo (C1-6) o fenil-[alcoxicarbonil-C1-6]-alquilo (C1- 6), Z1P(O)(OR9)2, Z2B(OR10)2, donde R9 y R10 en su caso significan hidrogeno o alquilo C1-6 y R10 en Z2B(OR10)2 pueden formar conjuntamente una cadena alquileno C2-4 o Z3COR11, donde R11 hidrogeno, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, cicloalquenilo C3-6, alquinilo C2-6, cicloalquinilo C3-6, hidroxi, alcoxi C1-6, alqueniloxi C3-6, alquiniloxi C3-6, amino, alquilamino C1-C6, [di- alquilo (C1-6)]amino, alcoxiamino C1-6, [di-(C1-6)-alcoxi]amino, alquilsulfonilamino C1-6, alquilamino C1-6sulfonilamino, [di-alquilamino (C1- 6)]sulfonilamino, alquenilamino C3-6, alquinilamino C3-6, N (alquenilo C2-6)-N-(alquil-C1-6)-amino, N-(alquinilo C2-6)-N-(alquil-C1- 6)-amino, N-(alcoxi C1-6)-N-(alquil-C1-6)-amino, N-(alquenilo C2-6)-N-(alcoxi-C1-6)-amino, N-(alquinilo C2-6)-N- (alcoxi-C1-6)-amino, fenilo, fenoxi, fenilamino, naftilo o heterociclilo; o Z4NR12R13, donde R12 y R13 independientemente entre sí significan hidrogeno, alquilo C1-6, cicloalquilo C3-6, alquenilo C3-6, cicloalquenilo C3-6, alquinilo C3-6, cicloalquinilo C3-6, alquilcarbonilo C1-6, cicloalquilcarbonilo C3-6, [di-alquilamino (C1-6)}carbonilo, alcoxicarbonilo C1-6, alcoxicarbonil- C1-6-alquilo (C1-6), alquilsulfonilo C1-6, alquilaminosulfonilo C1-6, [di-alquilamino (C1-6)]sulfonilo, fenilcarbonilo, fenilaminocarbonilo, fenilsulfonilo, fenilsulfonilaminocarbonilo o heterociclilcarbonilo; o Z5CH=N-O-R14, donde R14 significa hidrogeno o alquilo C1-6 o Z6OR15, donde R15 es hidrogeno, alquilo C1-6, cicloalquilo C3-6, alquenilo C3- 6, cicloalquenilo C3-6, alquinilo C3-6, cicloalquinilo C3-6, alquilcarbonilo C1-6, alcoxicarbonil-C1-6-alquilo (C1-6), [di-alcoxicarbonil-(C1-6)]- alquilo (C1-6), fenilo o fenil-alquilo (C1-6); o Z7SO2R16, donde R16 significa alquilo C1-6 o fenilo; y donde Z1, Z2, Z3, Z4, Z5, Z6, Z7 independientemente entre sí significan una union, -CH2-, -CH2-CH2, -O-CH(R17)-, -S-CH(R18)-, -S(O)-CH(R19)- o -SO2CH(R20)-, y donde R17, R18, R19 y R20 independientemente entre sí significan hidrogeno o alquilo C1-6 y donde las partes alifáticas, cíclicas o aromáticas mencionadas del sustituyente Ra pueden estar halogenadas en forma parcial o total y/o pueden portar uno a tres de los siguientes grupos: ciano, hidroxi, alquilo C1-4, haloalquilo C1- 4, cicloalquilo C3-6, alcoxi C1-4, alquiltio C1-4, [di-alquil-(C1- 4)]-amino, alquilcarbonilo C1-4, hidroxicarbonilo, alcoxicarbonilo C1-4, aminocarbonilo, alquilaminocarbonilo C1-4, [di-alquil-(C1-4)]aminocarbonilo o alquilcarboniloxi C1-4; y Rb, Rc, Rd, Re y Rf en cada caso independientemente entre sí equivalen a hidrogeno o tienen un significado indicado para Ra y donde dos restos Ra, Rb o Rc unidos a átomos cíclicos adyacentes A1 o dos restos Rd, Re o Rf unidos a átomos cíclicos adyacentes A2 también representan alquileno C3-6 lineal, que puede estar total o parcialmente halogenada y que pueden portar uno a tres de los siguientes grupos: ciano, hidroxi, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, alcoxi C1-4, alquiltio C1-4, [di-alquil-(C1-4)]-amino, alquilcarbonilo C1-4, hidroxicarbonilo, alcoxicarbonilo C1-4, aminocarbonilo, alquilaminocarbonilo C1-4, [di-alquil-(C1-4)]aminocarbonilo o alquilcarboniloxi C1-4, donde un grupo CH2 en alquileno-C3-6 puede estar sustituido con un grupo carbonilo, grupo tiocarbonilo o grupo sulfonilo y donde uno o dos grupos CH2 no adyacentes en alquileno-C3-6 pueden estar sustituidos en cada caso con oxigeno, azufre o un grupo NR34, donde R34 presenta un significado indicado para R12.
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| BRPI0812955A2 (pt) * | 2007-06-12 | 2014-12-09 | Basf Se | Compostos de piperazina, uso de um composto de piperazina, composição, e, método para combater vegetação indesejada |
| JP2010529168A (ja) * | 2007-06-12 | 2010-08-26 | ビーエーエスエフ ソシエタス・ヨーロピア | 除草作用を有するピペラジン化合物 |
| CL2008001864A1 (es) * | 2007-06-22 | 2009-09-25 | Basf Se | Compuestos derivados de piperazina -2,5-dionas; agente herbicida que los contiene; procedimiento de preparacion de dichos agentes herbicidas; uso de dichos compuestos; y procedeimiento para combatir el crecimiento de plantas no deseadas |
| US8097712B2 (en) | 2007-11-07 | 2012-01-17 | Beelogics Inc. | Compositions for conferring tolerance to viral disease in social insects, and the use thereof |
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| EP2318379A1 (de) | 2008-08-13 | 2011-05-11 | Basf Se | Verfahren zur herstellung von piperazindion-derivaten |
| KR20110063849A (ko) | 2008-10-02 | 2011-06-14 | 바스프 에스이 | 제초 효과를 갖는 피페라진 화합물 |
| KR20110080178A (ko) * | 2008-10-31 | 2011-07-12 | 바스프 에스이 | 제초 효과를 갖는 피페라진 화합물 |
| WO2010069819A1 (de) * | 2008-12-19 | 2010-06-24 | Basf Se | Verfahren zur herstellung von piperazindion-derivaten |
| 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 |
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| WO2013040057A1 (en) | 2011-09-13 | 2013-03-21 | Monsanto Technology Llc | Methods and compositions for weed control |
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| US10829828B2 (en) | 2011-09-13 | 2020-11-10 | Monsanto Technology Llc | Methods and compositions for weed control |
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| BR112014005795A2 (pt) | 2011-09-13 | 2020-12-08 | Monsanto Technology Llc | métodos de controle de plantas, de redução da expressão de um gene de hppd de uma planta, de preparação de um nucleotídeo, e de identificação de polinucleotídeos úteis na modulação da expressão do gene de hppd no tratamento externo de uma planta, composições e cassete de expressão microbiana |
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| CA2848669A1 (en) | 2011-09-13 | 2013-03-21 | Monsanto Technology Llc | Methods and compositions for weed control targeting epsps |
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