BR112017001433B1 - Amidas de ácido arilcarboxílico bicíclico e seu uso como herbicidas - Google Patents
Amidas de ácido arilcarboxílico bicíclico e seu uso como herbicidas Download PDFInfo
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- BR112017001433B1 BR112017001433B1 BR112017001433-5A BR112017001433A BR112017001433B1 BR 112017001433 B1 BR112017001433 B1 BR 112017001433B1 BR 112017001433 A BR112017001433 A BR 112017001433A BR 112017001433 B1 BR112017001433 B1 BR 112017001433B1
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- Brazil
- Prior art keywords
- alkyl
- halo
- alkoxy
- cycloalkyl
- heterocyclyl
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- 239000004009 herbicide Substances 0.000 title claims description 20
- 150000001408 amides Chemical class 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 52
- 238000000034 method Methods 0.000 claims abstract description 23
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 196
- -1 cyano, formyl Chemical group 0.000 claims description 189
- 229910052736 halogen Inorganic materials 0.000 claims description 80
- 150000002367 halogens Chemical group 0.000 claims description 80
- 125000000623 heterocyclic group Chemical group 0.000 claims description 53
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 49
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 45
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 44
- 239000001257 hydrogen Substances 0.000 claims description 43
- 229910052739 hydrogen Inorganic materials 0.000 claims description 43
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 39
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 35
- 150000003839 salts Chemical class 0.000 claims description 35
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 34
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 32
- 229910052760 oxygen Inorganic materials 0.000 claims description 32
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 30
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 30
- 125000001072 heteroaryl group Chemical group 0.000 claims description 29
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 28
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 28
- 239000001301 oxygen Substances 0.000 claims description 28
- 125000004043 oxo group Chemical group O=* 0.000 claims description 24
- 230000009261 transgenic effect Effects 0.000 claims description 21
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- 238000009472 formulation Methods 0.000 claims description 18
- 230000002363 herbicidal effect Effects 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 125000002619 bicyclic group Chemical group 0.000 claims description 16
- 244000038559 crop plants Species 0.000 claims description 16
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 16
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 16
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 14
- 125000006557 (C2-C5) alkylene group Chemical group 0.000 claims description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 13
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 12
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 11
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 10
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 10
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 8
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 8
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims description 8
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 8
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 claims description 7
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 6
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 6
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims description 6
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- 101100044057 Mesocricetus auratus SYCP3 gene Proteins 0.000 claims description 6
- 101100080600 Schizosaccharomyces pombe (strain 972 / ATCC 24843) nse6 gene Proteins 0.000 claims description 6
- GRHZLQBPAJAHDM-SPRQWYLLSA-N [(3as,4r,6ar)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-4-yl] n-[(2s,4s,5s)-5-[[2-(2,6-dimethylphenoxy)acetyl]amino]-4-hydroxy-1,6-diphenylhexan-2-yl]carbamate Chemical compound CC1=CC=CC(C)=C1OCC(=O)N[C@H]([C@@H](O)C[C@H](CC=1C=CC=CC=1)NC(=O)O[C@@H]1[C@@H]2CCO[C@@H]2OC1)CC1=CC=CC=C1 GRHZLQBPAJAHDM-SPRQWYLLSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 150000001721 carbon Chemical group 0.000 claims description 6
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- RFMQOHXWHFHOJF-UHFFFAOYSA-N cyano thiocyanate Chemical group N#CSC#N RFMQOHXWHFHOJF-UHFFFAOYSA-N 0.000 claims description 6
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims description 6
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 5
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 4
- HCUOEKSZWPGJIM-YBRHCDHNSA-N (e,2e)-2-hydroxyimino-6-methoxy-4-methyl-5-nitrohex-3-enamide Chemical compound COCC([N+]([O-])=O)\C(C)=C\C(=N/O)\C(N)=O HCUOEKSZWPGJIM-YBRHCDHNSA-N 0.000 claims description 4
- 125000001766 1,2,4-oxadiazol-3-yl group Chemical group [H]C1=NC(*)=NO1 0.000 claims description 4
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
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- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 4
- NWBNORAVIXIZTL-UHFFFAOYSA-N nitro thiocyanate Chemical compound [O-][N+](=O)SC#N NWBNORAVIXIZTL-UHFFFAOYSA-N 0.000 claims description 4
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 4
- 125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims description 3
- 239000013543 active substance Substances 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
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- 125000005843 halogen group Chemical group 0.000 claims description 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Chemical group SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 3
- 239000002917 insecticide Substances 0.000 claims description 3
- 239000000575 pesticide Substances 0.000 claims description 3
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims description 2
- 230000000895 acaricidal effect Effects 0.000 claims description 2
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- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- OAWUUPVZMNKZRY-UHFFFAOYSA-N cyprosulfamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC2CC2)C=C1 OAWUUPVZMNKZRY-UHFFFAOYSA-N 0.000 claims description 2
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims description 2
- 239000000417 fungicide Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical group C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 claims description 2
- 230000001012 protector Effects 0.000 claims description 2
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 claims description 2
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 claims 2
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- 125000002971 oxazolyl group Chemical group 0.000 description 1
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- 239000007800 oxidant agent Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
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- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
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- 125000000565 sulfonamide group Chemical group 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
- C07D257/06—Five-membered rings with nitrogen atoms directly attached to the ring carbon atom
-
- 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
- A01N43/82—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 three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
- C07D249/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/08—1,2,5-Oxadiazoles; Hydrogenated 1,2,5-oxadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
- C07D271/113—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D409/12—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 chain containing hetero atoms as chain links
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14178795 | 2014-07-28 | ||
| EP14178795.2 | 2014-07-28 | ||
| PCT/EP2015/066955 WO2016016107A1 (de) | 2014-07-28 | 2015-07-24 | Bicyclische arylcarbonsäureamide und ihre verwendung als herbizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR112017001433A2 BR112017001433A2 (pt) | 2017-12-05 |
| BR112017001433B1 true BR112017001433B1 (pt) | 2021-08-10 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR112017001433-5A BR112017001433B1 (pt) | 2014-07-28 | 2015-07-24 | Amidas de ácido arilcarboxílico bicíclico e seu uso como herbicidas |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US9914710B2 (enExample) |
| EP (1) | EP3174871B1 (enExample) |
| JP (1) | JP6643315B2 (enExample) |
| CN (1) | CN106715403B (enExample) |
| AR (1) | AR101230A1 (enExample) |
| AU (1) | AU2015295590A1 (enExample) |
| BR (1) | BR112017001433B1 (enExample) |
| CA (1) | CA2956302A1 (enExample) |
| EA (1) | EA201790281A1 (enExample) |
| MX (1) | MX2017001320A (enExample) |
| WO (1) | WO2016016107A1 (enExample) |
| ZA (1) | ZA201700704B (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018114663A1 (de) | 2016-12-22 | 2018-06-28 | Bayer Cropscience Aktiengesellschaft | Substituierte azolylpyrrolone und azolylhydantoine sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| US20200196601A1 (en) * | 2017-05-04 | 2020-06-25 | Bayer Cropscience Aktiengesellschaft | Herbicide safener compositions containing quinazolinedione-6carbonyl derivatives |
| BR112020017575A2 (pt) * | 2018-02-28 | 2020-12-22 | Bayer Aktiengesellschaft | Benzamidas bicíclicas herbicidamente ativas |
| CN110669016B (zh) * | 2018-09-29 | 2021-05-25 | 山东先达农化股份有限公司 | 三酮类化合物及其制备方法和应用以及一种除草剂 |
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| JPS4924073B2 (enExample) * | 1971-06-12 | 1974-06-20 | Adeka Argus Chemical Co Ltd | |
| CN1153515A (zh) * | 1994-06-10 | 1997-07-02 | 拜尔公司 | N-杂环基-杂芳氧基乙酰胺 |
| EP1101758A4 (en) * | 1998-07-28 | 2002-04-03 | Nihon Nohyaku Co Ltd | CONDENSED HETEROCYCLIC DICARBONIC ACID DIAMOND DERIVATIVES OR SALTS THEREOF, HERBICIDES AND THEIR USE |
| DK2611785T3 (da) * | 2010-09-01 | 2014-08-25 | Bayer Ip Gmbh | N-(tetrazol-5yl)- og n- (triazol-5-yl) arylcarboxylsyreamider og deres anvendelse som herbicider |
| EA023169B1 (ru) * | 2011-03-15 | 2016-04-29 | Байер Интеллектуэль Проперти Гмбх | Амиды n-(1,2,5-оксадиазол-3-ил)-, n-(тетразол-5-ил)- и n-(триазол-5-ил)бициклоарилкарбоновых кислот и гербицидные средства |
| PT2688885T (pt) * | 2011-03-22 | 2016-09-06 | Bayer Ip Gmbh | Amidas de ácido n-(1,3,4-oxadiazol-2-il)-arilcarboxílico e a utilização das mesmas como herbicidas |
| EP2589598A1 (de) * | 2011-11-03 | 2013-05-08 | Bayer CropScience AG | 5-Phenylsubstituierte N-(Tetrazol-5-yl)- und N-(Triazol-5-yl)arylcarbonsäureamide und ihre Verwendung als Herbizide |
| AU2012338879A1 (en) * | 2011-11-16 | 2014-06-05 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides II |
| WO2013072450A1 (en) * | 2011-11-18 | 2013-05-23 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides iii |
| PL2793589T3 (pl) * | 2011-12-21 | 2018-05-30 | Syngenta Limited | Związki herbicydowe |
| BR112014026823A2 (pt) * | 2012-04-27 | 2017-06-27 | Basf Se | compostos de n-(tetrazol-5-il) e n-(triazol-5-il)arilcarboxamida substituída e seu uso como herbicidas. |
| US20150216171A1 (en) * | 2012-09-05 | 2015-08-06 | Bayer Cropscience Ag | Herbicidally active bicycloaryl carboxylic acid amides |
| WO2014086737A1 (de) * | 2012-12-06 | 2014-06-12 | Bayer Cropscience Ag | Kondensierte 2-pyridon-3-carboxamide und ihre verwendung als herbizide |
| WO2014086746A1 (de) * | 2012-12-07 | 2014-06-12 | Bayer Cropscience Ag | N-(isoxazol-3-yl)-arylcarbonsäureamide und ihre verwendung als herbizide |
-
2015
- 2015-07-17 AR ARP150102275A patent/AR101230A1/es unknown
- 2015-07-24 EP EP15738948.7A patent/EP3174871B1/de active Active
- 2015-07-24 BR BR112017001433-5A patent/BR112017001433B1/pt active IP Right Grant
- 2015-07-24 CA CA2956302A patent/CA2956302A1/en not_active Abandoned
- 2015-07-24 MX MX2017001320A patent/MX2017001320A/es unknown
- 2015-07-24 US US15/328,253 patent/US9914710B2/en active Active
- 2015-07-24 CN CN201580051066.6A patent/CN106715403B/zh active Active
- 2015-07-24 JP JP2017504417A patent/JP6643315B2/ja active Active
- 2015-07-24 AU AU2015295590A patent/AU2015295590A1/en not_active Abandoned
- 2015-07-24 EA EA201790281A patent/EA201790281A1/ru unknown
- 2015-07-24 WO PCT/EP2015/066955 patent/WO2016016107A1/de not_active Ceased
-
2017
- 2017-01-27 ZA ZA2017/00704A patent/ZA201700704B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN106715403A (zh) | 2017-05-24 |
| JP2017523186A (ja) | 2017-08-17 |
| CA2956302A1 (en) | 2016-02-04 |
| AU2015295590A1 (en) | 2017-02-16 |
| BR112017001433A2 (pt) | 2017-12-05 |
| EA201790281A1 (ru) | 2017-11-30 |
| AR101230A1 (es) | 2016-11-30 |
| JP6643315B2 (ja) | 2020-02-12 |
| US20170217909A1 (en) | 2017-08-03 |
| CN106715403B (zh) | 2020-06-02 |
| WO2016016107A1 (de) | 2016-02-04 |
| ZA201700704B (en) | 2018-05-30 |
| MX2017001320A (es) | 2017-05-09 |
| EP3174871A1 (de) | 2017-06-07 |
| EP3174871B1 (de) | 2018-11-21 |
| US9914710B2 (en) | 2018-03-13 |
| AU2015295590A2 (en) | 2017-03-16 |
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