JP2015508767A5 - - Google Patents
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- Publication number
- JP2015508767A5 JP2015508767A5 JP2014557065A JP2014557065A JP2015508767A5 JP 2015508767 A5 JP2015508767 A5 JP 2015508767A5 JP 2014557065 A JP2014557065 A JP 2014557065A JP 2014557065 A JP2014557065 A JP 2014557065A JP 2015508767 A5 JP2015508767 A5 JP 2015508767A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- halo
- heterocyclyl
- phenyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 434
- 229910052736 halogen Inorganic materials 0.000 claims description 42
- 150000002367 halogens Chemical class 0.000 claims description 42
- 229910052739 hydrogen Inorganic materials 0.000 claims description 41
- 239000001257 hydrogen Substances 0.000 claims description 41
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 38
- 125000000623 heterocyclic group Chemical group 0.000 claims description 36
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 34
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 30
- -1 cyano, thiocyanato Chemical group 0.000 claims description 28
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 24
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 24
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 20
- 125000001072 heteroaryl group Chemical group 0.000 claims description 20
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 17
- 125000004043 oxo group Chemical group O=* 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 13
- 150000002431 hydrogen Chemical class 0.000 claims description 13
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 11
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 8
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 6
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 2
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- RFMQOHXWHFHOJF-UHFFFAOYSA-N cyano thiocyanate Chemical compound N#CSC#N RFMQOHXWHFHOJF-UHFFFAOYSA-N 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 9
- 230000002363 herbicidal effect Effects 0.000 claims 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 125000005843 halogen group Chemical group 0.000 claims 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 150000003254 radicals Chemical class 0.000 claims 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
- FKTXDTWDCPTPHK-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical group FC(F)(F)[C](F)C(F)(F)F FKTXDTWDCPTPHK-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims 2
- 239000000460 chlorine Chemical group 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 125000004775 chlorodifluoromethyl group Chemical group FC(F)(Cl)* 0.000 claims 2
- 244000038559 crop plants Species 0.000 claims 2
- 125000004774 dichlorofluoromethyl group Chemical group FC(Cl)(Cl)* 0.000 claims 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 2
- 239000004009 herbicide Substances 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims 2
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 2
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims 2
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- 230000000895 acaricidal effect Effects 0.000 claims 1
- 239000000642 acaricide Substances 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 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 1
- 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 1
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 1
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 230000009261 transgenic effect Effects 0.000 claims 1
- 244000045561 useful plants Species 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12156310 | 2012-02-21 | ||
| EP12156310.0 | 2012-02-21 | ||
| PCT/EP2013/053151 WO2013124230A1 (de) | 2012-02-21 | 2013-02-18 | Herbizid wirksame sulfinimidoyl- und sulfonimidoylbenzoylderivate |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015508767A JP2015508767A (ja) | 2015-03-23 |
| JP2015508767A5 true JP2015508767A5 (enExample) | 2017-02-09 |
| JP6084988B2 JP6084988B2 (ja) | 2017-02-22 |
Family
ID=47716073
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014557065A Active JP6084988B2 (ja) | 2012-02-21 | 2013-02-18 | 除草剤スルフィンイミドイル−およびスルホンイミドイルベンゾイル誘導体 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9156784B2 (enExample) |
| EP (1) | EP2816896B1 (enExample) |
| JP (1) | JP6084988B2 (enExample) |
| CN (1) | CN104244713B (enExample) |
| AR (1) | AR090111A1 (enExample) |
| BR (1) | BR112014020601B1 (enExample) |
| WO (1) | WO2013124230A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2755484A1 (en) * | 2011-09-16 | 2014-07-23 | Bayer Intellectual Property GmbH | Use of 5-phenyl- or 5-benzyl-2 isoxazoline-3 carboxylates for improving plant yield |
| CN118812500A (zh) * | 2024-07-12 | 2024-10-22 | 东北农业大学 | 一种具有除草活性的取代芳基二酮腈类化合物、制备方法及应用 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60500438A (ja) | 1983-01-17 | 1985-04-04 | モンサント カンパニ− | 植物細胞を形質転換するためのプラスミド |
| BR8404834A (pt) | 1983-09-26 | 1985-08-13 | Agrigenetics Res Ass | Metodo para modificar geneticamente uma celula vegetal |
| BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
| ATE80182T1 (de) | 1985-10-25 | 1992-09-15 | Monsanto Co | Pflanzenvektoren. |
| DE3765449D1 (de) | 1986-03-11 | 1990-11-15 | Plant Genetic Systems Nv | Durch gentechnologie erhaltene und gegen glutaminsynthetase-inhibitoren resistente pflanzenzellen. |
| US5013659A (en) | 1987-07-27 | 1991-05-07 | E. I. Du Pont De Nemours And Company | Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase |
| IL83348A (en) | 1986-08-26 | 1995-12-08 | Du Pont | Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase |
| ATE241007T1 (de) | 1990-03-16 | 2003-06-15 | Calgene Llc | Dnas, die für pflanzliche desaturasen kodieren und deren anwendungen |
| ATE212670T1 (de) | 1990-06-18 | 2002-02-15 | Monsanto Technology Llc | Erhöhter stärkegehalt in pflanzen |
| EP0536330B1 (en) | 1990-06-25 | 2002-02-27 | Monsanto Technology LLC | Glyphosate tolerant plants |
| SE467358B (sv) | 1990-12-21 | 1992-07-06 | Amylogene Hb | Genteknisk foeraendring av potatis foer bildning av staerkelse av amylopektintyp |
| GB9310203D0 (en) | 1993-05-18 | 1993-06-30 | Rhone Poulenc Agriculture | Compositions of new matter |
| DE4104782B4 (de) | 1991-02-13 | 2006-05-11 | Bayer Cropscience Gmbh | Neue Plasmide, enthaltend DNA-Sequenzen, die Veränderungen der Karbohydratkonzentration und Karbohydratzusammensetzung in Pflanzen hervorrufen, sowie Pflanzen und Pflanzenzellen enthaltend dieses Plasmide |
| GB9302049D0 (en) | 1993-02-03 | 1993-03-24 | Rhone Poulenc Agriculture | Compositions of new matter |
| KR20040029410A (ko) | 2001-08-08 | 2004-04-06 | 바스프 악티엔게젤샤프트 | 벤조일시클로헥세논 유도체 |
| WO2004052849A1 (ja) | 2002-12-12 | 2004-06-24 | Nippon Soda Co.,Ltd. | スルホキシイミン基を有するベンゾイル誘導体および除草剤 |
| TW201309635A (zh) | 2006-02-10 | 2013-03-01 | Dow Agrosciences Llc | 殺蟲性之ｎ-取代（６-鹵烷基吡啶-３-基）烷基磺醯亞胺（二） |
| CL2008000376A1 (es) * | 2007-02-09 | 2008-08-18 | Du Pont | Compuestos derivados de n-oxidos de piridina; composicion herbicida; y metodo para controlar el crecimiento de vegetacion indeseada. |
| US7511149B2 (en) | 2007-02-09 | 2009-03-31 | Dow Agrosciences Llc | Process for the oxidation of certain substituted sulfilimines to insecticidal sulfoximines |
| BRPI0721218A2 (pt) | 2007-02-09 | 2013-01-01 | Dow Agrosciences Llc | processo para a oxidação de determinadas sulfiliminas substituìdas para sulfoximinas inseticidas |
| AU2008219748B2 (en) | 2007-02-26 | 2012-05-03 | Corteva Agriscience Llc | Process for the preparation of certain substituted sulfilimines |
| EP1980556A1 (de) * | 2007-04-12 | 2008-10-15 | Bayer CropScience AG | 4-(4-Trifluormethyl-3-thiobenzoyl)pyrazole und ihre Verwendung als Herbizide |
| WO2008141843A1 (en) | 2007-05-24 | 2008-11-27 | Bayer Schering Pharma Aktiengesellschaft | Novel sulphoximine-substituted quinazoline and quinazoline derivatives as kinase inhibitors |
| EP2127521A1 (de) | 2008-05-29 | 2009-12-02 | Bayer CropScience Aktiengesellschaft | Herbizid wirksame 4-(3-Alkylsulfinylbenzoyl)pyrazole |
| WO2010016230A1 (ja) | 2008-08-05 | 2010-02-11 | 日本曹達株式会社 | スルホキシイミノ置換ベンゾイル誘導体及び除草剤 |
| ES2622872T3 (es) | 2008-08-27 | 2017-07-07 | Dow Agrosciences Llc | Composiciones plaguicidas que comprenden sulfoximinas N-sustituidas |
| EP2475646B1 (de) * | 2009-07-29 | 2017-06-21 | Bayer Intellectual Property GmbH | 4- (3-alkylthiobenzoyl) pyrazole und ihre verwendung als herbizide |
| KR101767519B1 (ko) | 2009-07-29 | 2017-08-11 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 2-(3-알킬티오벤조일)사이클로헥산디온 및 제초제로서의 그의 용도 |
| JP5280972B2 (ja) * | 2009-08-20 | 2013-09-04 | 日本曹達株式会社 | 殺ダニ剤および新規ウレア化合物 |
| WO2012010574A1 (de) * | 2010-07-21 | 2012-01-26 | Bayer Cropscience Ag | (4-trifluormethyl-3-thiobenzoyl)cyclohexandione und ihre verwendung als herbizide |
| WO2013124228A1 (de) * | 2012-02-21 | 2013-08-29 | Bayer Intellectual Property Gmbh | Herbizid wirksame 3 - ( sulfin- /sulfonimidoyl) - benzamide |
-
2013
- 2013-02-18 CN CN201380020923.7A patent/CN104244713B/zh active Active
- 2013-02-18 BR BR112014020601-5A patent/BR112014020601B1/pt active IP Right Grant
- 2013-02-18 JP JP2014557065A patent/JP6084988B2/ja active Active
- 2013-02-18 US US14/379,513 patent/US9156784B2/en active Active
- 2013-02-18 EP EP13704465.7A patent/EP2816896B1/de active Active
- 2013-02-18 WO PCT/EP2013/053151 patent/WO2013124230A1/de not_active Ceased
- 2013-02-21 AR ARP130100526A patent/AR090111A1/es unknown
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