AR039004A1 - Herbicidas selectivos a base de aminotriazinonas substituidas y de benzoilciclohexanodionas substituidas - Google Patents
Herbicidas selectivos a base de aminotriazinonas substituidas y de benzoilciclohexanodionas substituidasInfo
- Publication number
- AR039004A1 AR039004A1 ARP030100940A ARP030100940A AR039004A1 AR 039004 A1 AR039004 A1 AR 039004A1 AR P030100940 A ARP030100940 A AR P030100940A AR P030100940 A ARP030100940 A AR P030100940A AR 039004 A1 AR039004 A1 AR 039004A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- case
- phenyl
- substituted
- dichloro
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 244000038559 crop plants Species 0.000 abstract 3
- MHULQDZDXMHODA-UHFFFAOYSA-N 1-(2,2-dichloroacetyl)-3,3,8a-trimethyl-2,4,7,8-tetrahydropyrrolo[1,2-a]pyrimidin-6-one Chemical compound C1C(C)(C)CN(C(=O)C(Cl)Cl)C2(C)N1C(=O)CC2 MHULQDZDXMHODA-UHFFFAOYSA-N 0.000 abstract 2
- -1 1-methyl-hexyl ester Chemical class 0.000 abstract 2
- QWWHRELOCZEQNZ-UHFFFAOYSA-N 2,2-dichloro-1-(1-oxa-4-azaspiro[4.5]decan-4-yl)ethanone Chemical compound ClC(Cl)C(=O)N1CCOC11CCCCC1 QWWHRELOCZEQNZ-UHFFFAOYSA-N 0.000 abstract 2
- MCNOFYBITGAAGM-UHFFFAOYSA-N 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound C1N(C(=O)C(Cl)Cl)C(C)(C)OC1C1=CC=CO1 MCNOFYBITGAAGM-UHFFFAOYSA-N 0.000 abstract 2
- ZAWPDPLWGKAAHU-UHFFFAOYSA-N 2,2-dichloro-n-[2-oxo-2-(prop-2-enylamino)ethyl]-n-prop-2-enylacetamide Chemical compound ClC(Cl)C(=O)N(CC=C)CC(=O)NCC=C ZAWPDPLWGKAAHU-UHFFFAOYSA-N 0.000 abstract 2
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 abstract 2
- OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 abstract 2
- XKLPBDMZJSWRBL-UHFFFAOYSA-N 3-benzoylcyclohexane-1,2-dione Chemical class C=1C=CC=CC=1C(=O)C1CCCC(=O)C1=O XKLPBDMZJSWRBL-UHFFFAOYSA-N 0.000 abstract 2
- VKJMPYGLTDMUPZ-UHFFFAOYSA-N 5-amino-1h-triazin-6-one Chemical class NC1=CN=NNC1=O VKJMPYGLTDMUPZ-UHFFFAOYSA-N 0.000 abstract 2
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 abstract 2
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 abstract 2
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 abstract 2
- YNQSILKYZQZHFJ-UHFFFAOYSA-N R-29148 Chemical compound CC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 YNQSILKYZQZHFJ-UHFFFAOYSA-N 0.000 abstract 2
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical compound CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical compound C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- OISQRMLHYOLTJL-UHFFFAOYSA-N 2,2-dichloro-n-(1,3-dioxolan-2-ylmethyl)-n-prop-2-enylacetamide Chemical compound ClC(Cl)C(=O)N(CC=C)CC1OCCO1 OISQRMLHYOLTJL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract 1
- HCEJOAJCHSLTDV-UHFFFAOYSA-N 2-(8-chloroquinoxalin-5-yl)oxyacetic acid Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=N1 HCEJOAJCHSLTDV-UHFFFAOYSA-N 0.000 abstract 1
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 abstract 1
- GMBRUAIJEFRHFQ-UHFFFAOYSA-N Fenchlorazole-ethyl Chemical compound N1=C(C(=O)OCC)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl GMBRUAIJEFRHFQ-UHFFFAOYSA-N 0.000 abstract 1
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005574 MCPA Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 abstract 1
- 230000002708 enhancing effect Effects 0.000 abstract 1
- COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- CMCJQHLLWDPWPK-UHFFFAOYSA-N n-[4-(cyclopropylcarbamoyl)phenyl]sulfonyl-2-methoxy-5-methylbenzamide Chemical compound COC1=CC=C(C)C=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC2CC2)C=C1 CMCJQHLLWDPWPK-UHFFFAOYSA-N 0.000 abstract 1
- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 230000002195 synergetic effect Effects 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/707—1,2,3- or 1,2,4-triazines; Hydrogenated 1,2,3- or 1,2,4-triazines
Landscapes
- 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
La presente se refiere a nuevas combinaciones de productos activos herbicidas, sinérgicas, que comprenden, por un lado, aminotriazinonas sustituidas, conocidas, y, por otro lado, benzoilciclohexanodionas sustituidas, conocidas y , si fuera adecuado además un compuesto mejorador de la compatibilidad para con las plantas de cultivo y que pueden emplearse, con un éxito especialmente bueno para la lucha selectiva contra las malas hierbas en diversos cultivos de plantas útiles. Reivindicación 1: Agentes herbicidas, caracterizados porque tienen un contenido activo de una combinación de productos activos, que comprende: a) al menos una aminotriazinona sustituida de la fórmula general (1) en la que: R1' significa alquilo de cadena lineal o de cadena ramificada con 1 hasta 6 átomos de carbono o significa fenilo; y R2 significa en cada caso alquilo o alquiltio, respectivamente de cadena lineal o de cadena ramifica con 1 hasta 6 átomos de carbono, ("productos activos del grupo 1"); y b) al menos una benzoilciclohexanodiona sustituida de la fórmula (2) en la que: R3 significa nitro, ciano, halógeno, o significa en cada caso, alquilo, alcoxi, alquiltio, alquilsulfinilo o alquilsulfonilo en cada caso con 1 hasta 6 átomos de carbono, en cada caso de cadena lineal o de cadena ramificada, sustituidos por halógeno; y R4 significa nitro, ciano, halógeno, significa en cada caso alquilo, alcoxi, alquiltio, alquilsulfinilo o alquilsulfonilo en cada caso con 1 hasta 6 átomos de carbono, opcionalmente sustituidos por halógeno, por alcoxi C1-4, por alquiltio C1-4, por alquilsulfinilo C1-4 o por alquilsulfonilo C1-4, en cada caso de cadena lineal o de cadena ramificada, o significa alquilamino, dialquilamino, dialquilaminocarbonilo o dialquilaminosulfonilo en cada caso con 1 hasta 6 átomos de carbono en los grupos alquilo, en cada caso de cadena lineal o de cadena ramificada, ("productos activos del grupo 2") así como, si fuera adecuado; además c) un compuesto mejorador de la compatibilidad para las plantas de cultivo del grupo siguiente de compuestos: 4-dicloroacetil-1-oxa-4-aza-spiro[4.5]-decano (AD-67), 1-dicloroacetil-hexahidro-3,3,8a-trimetilpirrolo[1,2-a]-pirimidin-6(2H)-ona (BAS-145138), 4-dicloroacetil-3,4-dihidro-3-metil-2H-1,4-benzoxazina (Benoxacor), ácido 5-cloro-quinoxalin-8-oxi-acético-(éster de 1-metil-hexilo) (Cloquintocet-mexilo), ?-(cianometoximino)-fenilacetonitrilo (Ciometrinil), ácido 2,4-dicloro-fenoxiacético (2,4-D), 2,2-dicloro-N-(2-oxo-2-(2-propenilamino)-etil)-N-(2-propenil)-acetamida (DKA-24), 2,2-dicloro-N,N-di-2-propenil-acetimida (Diclormid), N-(4-metil-fenil)-N'-(1-metil-1-fenil-etil)-urea (Daimuron, Dymron), 4,6-dicloro-2-fenil-pirimidina (Fenclorim), 1-(2,4-dicloro-fenil)-5-triclorometil-1H-1,2,4-triazol-3-carboxilato de etilo (Fenclorazol-etilo), 2-cloro-4-triflúormetil-tiazol-5-carboxilato de fenil-metilo (Flurazol), 4-cloro-N-(1,3-dioxolan-2-il-metoxi)-?-triflúor-acetofenonoxima (Fluxofenim), 3-dicloroacetil-5-(2-furanil)-2,2-dimetil-oxazolidina (Furilazol, MON-13900), etil-4,5-dihidro-5,5-difenil-3-isoxazolcarboxilato (Isoxadifen-etilo), ácido (4-cloro-2-metil-fenoxi)-acético (MCPA), ácido (+/-)-2-(4-cloro-2-metil-fenoxi)-propanoico (Mecoprop), dietil-1-(2,4-diclorofenil)-4,5-dihidro-5-metil-1H-pirazol-3,5-dicarboxilato (Mefenpir-dietilo), 2-diclorometil-2-metil-1,3-dioxolano (MG-191), anhídrido del ácido 1,8-naftálico, ?-(1,3-dioxolan-2-il-metoximino)-fenilacetonitrilo (Oxabetrinil), 2,2-dicloro-N-(1,3-dioxolan-2-il-metil)-N-(2-propenil)-acetamida (PPG-1292), 3-dicloroacetil-2,2,5-trimetil-oxazolidina (R-29148), N-ciclopropil-4-[[(2-metoxi-5-metil-benzoil)-amino]-sulfonil]-benzamida, N-[[(4-metoxiacetilamino)-fenil]-sulfonil]-2-metoxi-benzamida y N-[[(4-metilaminocarbonilamino)-fenil]-sulfonil]-2-metoxi-benzamida (estas últimas conocidas, en cada caso, por la WO-A-99/66795, ("productos activos del grupo 3").
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10212887A DE10212887A1 (de) | 2002-03-22 | 2002-03-22 | Selektive Herbizide auf Basis von substituierten Aminotriazinonen und substituierten Benzoylcyclohexandionen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR039004A1 true AR039004A1 (es) | 2005-02-02 |
Family
ID=27798090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030100940A AR039004A1 (es) | 2002-03-22 | 2003-03-18 | Herbicidas selectivos a base de aminotriazinonas substituidas y de benzoilciclohexanodionas substituidas |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7612017B2 (es) |
| EP (1) | EP1489907B1 (es) |
| AR (1) | AR039004A1 (es) |
| AT (1) | ATE468750T1 (es) |
| AU (1) | AU2003222756A1 (es) |
| BR (1) | BR0308661B1 (es) |
| DE (2) | DE10212887A1 (es) |
| MX (1) | MXPA04009156A (es) |
| WO (1) | WO2003079789A1 (es) |
| ZA (1) | ZA200407640B (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA117816C2 (uk) * | 2012-11-06 | 2018-10-10 | Байєр Кропсайєнс Акцієнгезелльшафт | Гербіцидна комбінація для толерантних соєвих культур |
| CA3016498A1 (en) | 2016-03-07 | 2017-09-14 | Bayer Cropscience Aktiengesellschaft | Herbicidal compositions containing active substances from the group comprising hppd inhibitors, safeners and triazines |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1542873C3 (de) * | 1966-04-16 | 1978-07-13 | Bayer Ag, 5090 Leverkusen | Herbizides Mittel auf Basis von 4-Amino-1,2,4-triazin-5-onen |
| US3966715A (en) * | 1966-04-16 | 1976-06-29 | Bayer Aktiengesellschaft | Herbicidal agents |
| CH495110A (de) * | 1966-04-16 | 1970-08-31 | Bayer Ag | Herbizides Mittel |
| US4036632A (en) * | 1966-04-16 | 1977-07-19 | Bayer Aktiengesellschaft | Herbicidal agents |
| US4346220A (en) * | 1966-11-28 | 1982-08-24 | E. I. Du Pont De Nemours And Company | 1,2,4-Triazin-5-ones |
| BE786840A (fr) * | 1971-07-29 | 1973-01-29 | Bayer Ag | Procede de preparation de 1,2,4-triazine -5-ones |
| US4946981A (en) * | 1982-03-25 | 1990-08-07 | Ici Americas Inc. | Certain 2-(2-substituted benzoyl)-1,3-cyclohexanediones |
| US4780127A (en) * | 1982-03-25 | 1988-10-25 | Stauffer Chemical Company | Certain 2-(substituted benzoyl)-1,3-cyclohexanediones and their use as herbicides |
| US5006162A (en) * | 1982-03-25 | 1991-04-09 | Ici Americas Inc. | Certain 2-(2-substituted benzoyl)-1,3,5-cyclohexanetriones |
| DE3937475A1 (de) * | 1989-11-10 | 1991-05-16 | Bayer Ag | Selektiv-herbizide mittel, enthaltend metribuzin in kombination mit bromoxynil |
| GB9313210D0 (en) * | 1993-06-25 | 1993-08-11 | Sandoz Ltd | Novel combinations |
| US5506195A (en) * | 1994-11-01 | 1996-04-09 | Zeneca Limited | Selective 1,3-cyclohexanedione corn herbicide |
| DE19827855A1 (de) * | 1998-06-23 | 1999-12-30 | Hoechst Schering Agrevo Gmbh | Kombinationen aus Herbiziden und Safenern |
| GB0022932D0 (en) | 2000-09-18 | 2000-11-01 | Aventis Cropscience Sa | New herbicidal composition |
| GB0114198D0 (en) * | 2001-06-11 | 2001-08-01 | Syngenta Ltd | Herbicidal composition |
| GB0116956D0 (en) | 2001-07-11 | 2001-09-05 | Syngenta Ltd | Weed control process |
| AU2002362498A1 (en) * | 2001-09-27 | 2003-04-14 | Syngenta Participations Ag | Herbicidal composition |
-
2002
- 2002-03-22 DE DE10212887A patent/DE10212887A1/de not_active Withdrawn
-
2003
- 2003-03-10 BR BRPI0308661-5B1A patent/BR0308661B1/pt active IP Right Grant
- 2003-03-10 DE DE50312742T patent/DE50312742D1/de not_active Expired - Lifetime
- 2003-03-10 AT AT03718682T patent/ATE468750T1/de active
- 2003-03-10 WO PCT/EP2003/002416 patent/WO2003079789A1/de not_active Ceased
- 2003-03-10 MX MXPA04009156A patent/MXPA04009156A/es active IP Right Grant
- 2003-03-10 EP EP03718682A patent/EP1489907B1/de not_active Expired - Lifetime
- 2003-03-10 AU AU2003222756A patent/AU2003222756A1/en not_active Abandoned
- 2003-03-10 US US10/508,503 patent/US7612017B2/en not_active Expired - Fee Related
- 2003-03-18 AR ARP030100940A patent/AR039004A1/es unknown
-
2004
- 2004-09-21 ZA ZA2004/07640A patent/ZA200407640B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR0308661A (pt) | 2005-02-15 |
| US20050143261A1 (en) | 2005-06-30 |
| EP1489907B1 (de) | 2010-05-26 |
| AU2003222756A1 (en) | 2003-10-08 |
| EP1489907A1 (de) | 2004-12-29 |
| BR0308661B1 (pt) | 2013-12-10 |
| DE50312742D1 (de) | 2010-07-08 |
| ZA200407640B (en) | 2005-11-30 |
| WO2003079789A1 (de) | 2003-10-02 |
| US7612017B2 (en) | 2009-11-03 |
| DE10212887A1 (de) | 2003-10-02 |
| MXPA04009156A (es) | 2004-12-07 |
| ATE468750T1 (de) | 2010-06-15 |
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Legal Events
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| FB | Suspension of granting procedure |