JP2018529702A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2018529702A5 JP2018529702A5 JP2018515805A JP2018515805A JP2018529702A5 JP 2018529702 A5 JP2018529702 A5 JP 2018529702A5 JP 2018515805 A JP2018515805 A JP 2018515805A JP 2018515805 A JP2018515805 A JP 2018515805A JP 2018529702 A5 JP2018529702 A5 JP 2018529702A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- cycloalkyl
- alkylthio
- alkylsulfinyl
- 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 80
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 48
- -1 cyano, nitro , Hydroxy, amino, carboxy, carbamoyl Chemical group 0.000 claims 34
- 125000001424 substituent group Chemical group 0.000 claims 32
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 27
- 229910052736 halogen Inorganic materials 0.000 claims 26
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 24
- 150000002367 halogens Chemical class 0.000 claims 24
- 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 claims 22
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 20
- 125000001072 heteroaryl group Chemical group 0.000 claims 19
- 125000004093 cyano group Chemical group *C#N 0.000 claims 16
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 15
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 15
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 14
- 125000003282 alkyl amino group Chemical group 0.000 claims 14
- 229910052739 hydrogen Inorganic materials 0.000 claims 14
- 239000001257 hydrogen Substances 0.000 claims 14
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 13
- 125000005159 cyanoalkoxy group Chemical group 0.000 claims 13
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 12
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 12
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims 12
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims 12
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 11
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 11
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 11
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 11
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 11
- 125000004414 alkyl thio group Chemical group 0.000 claims 11
- 150000002431 hydrogen Chemical class 0.000 claims 11
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 10
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 10
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 10
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 10
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 10
- 125000005103 alkyl silyl group Chemical group 0.000 claims 10
- 125000000232 haloalkynyl group Chemical group 0.000 claims 10
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 10
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 9
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 9
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 9
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 9
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims 9
- 125000003118 aryl group Chemical group 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 9
- 125000000262 haloalkenyl group Chemical group 0.000 claims 9
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 229920006395 saturated elastomer Polymers 0.000 claims 9
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 8
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 8
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 8
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 claims 8
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 8
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 8
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 8
- 125000004683 alkyl sulfoxy imino group Chemical group 0.000 claims 8
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 8
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 8
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 8
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 8
- 125000004758 (C1-C4) alkoxyimino group Chemical group 0.000 claims 7
- 125000004760 (C1-C4) alkylsulfonylamino group Chemical group 0.000 claims 7
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims 7
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 7
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 7
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 7
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims 7
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 7
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 claims 7
- 125000004995 haloalkylthio group Chemical group 0.000 claims 7
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims 6
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 claims 6
- 125000005089 alkenylaminocarbonyl group Chemical group 0.000 claims 6
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims 6
- 229910052801 chlorine Inorganic materials 0.000 claims 6
- 239000000460 chlorine Substances 0.000 claims 6
- 125000004122 cyclic group Chemical group 0.000 claims 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 5
- 229910052799 carbon Inorganic materials 0.000 claims 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 5
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 5
- 239000003905 agrochemical Substances 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 125000002619 bicyclic group Chemical group 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 125000005842 heteroatom Chemical group 0.000 claims 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 241000607479 Yersinia pestis Species 0.000 claims 3
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 claims 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 3
- 229910052794 bromium Inorganic materials 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 3
- 239000011737 fluorine Substances 0.000 claims 3
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 3
- LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 claims 2
- CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000006001 difluoroethyl group Chemical group 0.000 claims 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 2
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims 2
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 2
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 claims 1
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000005153 alkyl sulfamoyl group Chemical group 0.000 claims 1
- 150000008051 alkyl sulfates Chemical class 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 125000004788 dichlorofluoromethoxy group Chemical group ClC(O*)(F)Cl 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000006337 tetrafluoro ethyl group Chemical group 0.000 claims 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15187145 | 2015-09-28 | ||
| EP15187145.6 | 2015-09-28 | ||
| PCT/EP2016/072697 WO2017055185A1 (de) | 2015-09-28 | 2016-09-23 | 2-(het)aryl-substituierte kondensierte heterocyclen-derivate als schädlingsbekämpfungsmittel |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018529702A JP2018529702A (ja) | 2018-10-11 |
| JP2018529702A5 true JP2018529702A5 (enExample) | 2019-10-31 |
| JP6871917B2 JP6871917B2 (ja) | 2021-05-19 |
Family
ID=54207414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018515805A Active JP6871917B2 (ja) | 2015-09-28 | 2016-09-23 | 有害生物防除剤としての２−（ヘタ）アリール−置換縮合二環式ヘテロ環誘導体 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US10745398B2 (enExample) |
| EP (1) | EP3356362B1 (enExample) |
| JP (1) | JP6871917B2 (enExample) |
| KR (1) | KR102629107B1 (enExample) |
| CN (1) | CN108290886B (enExample) |
| AR (1) | AR106165A1 (enExample) |
| AU (1) | AU2016330299B2 (enExample) |
| BR (1) | BR112018006198B1 (enExample) |
| CA (1) | CA2999790A1 (enExample) |
| CL (1) | CL2018000741A1 (enExample) |
| CO (1) | CO2018003427A2 (enExample) |
| ES (1) | ES2866911T3 (enExample) |
| IL (1) | IL258089A (enExample) |
| MX (1) | MX2018003761A (enExample) |
| PE (1) | PE20181094A1 (enExample) |
| PH (1) | PH12018500638B1 (enExample) |
| RU (1) | RU2018116054A (enExample) |
| TW (1) | TWI720023B (enExample) |
| UY (1) | UY36918A (enExample) |
| WO (1) | WO2017055185A1 (enExample) |
| ZA (1) | ZA201802797B (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017065183A1 (ja) * | 2015-10-13 | 2017-04-20 | 日本農薬株式会社 | オキシム基を有する縮合複素環化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法 |
| RU2018129199A (ru) | 2016-01-11 | 2020-02-13 | Байер Кропсайенс Акциенгезельшафт | Гетероциклические производные в качестве средства для борьбы с вредителями |
| MX2019001918A (es) | 2016-08-15 | 2019-09-06 | Bayer Cropscience Ag | Derivados del heterociclo biciclico condensado como agentes de control de plagas. |
| TWI762568B (zh) | 2017-02-06 | 2022-05-01 | 德商拜耳作物科學股份有限公司 | 製備鹵化咪唑並吡啶衍生物之方法 |
| TW201833107A (zh) | 2017-02-06 | 2018-09-16 | 德商拜耳廠股份有限公司 | 作為殺蟲劑之經２－（雜）芳基取代的稠合雜環衍生物 |
| US11203590B2 (en) | 2017-07-13 | 2021-12-21 | Sumitomo Chemical Company, Limited | Heterocyclic compound and harmful-arthropod control agent containing same |
| EP3733672B1 (en) | 2017-12-25 | 2023-03-22 | Sumitomo Chemical Company, Limited | Heterocyclic compounds and noxious arthropod control agent containing same |
| WO2019131575A1 (ja) | 2017-12-26 | 2019-07-04 | 住友化学株式会社 | 複素環化合物及びそれを含有する有害節足動物防除剤 |
| WO2019138018A1 (en) | 2018-01-15 | 2019-07-18 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| US11019821B2 (en) | 2018-02-21 | 2021-06-01 | Bayer Aktiengesellschaft | Fused bicyclic heterocycle derivatives as pesticides |
| ES2980209T3 (es) | 2018-06-26 | 2024-09-30 | Bayer Ag | Derivados heterocíclicos como plaguicidas |
| JP7399589B2 (ja) * | 2018-09-12 | 2023-12-18 | 日本化薬株式会社 | 有害生物防除剤 |
| WO2021009311A1 (en) | 2019-07-17 | 2021-01-21 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2021033141A1 (en) | 2019-08-20 | 2021-02-25 | Pi Industries Ltd. | Fused heterocyclic compounds and their use as pest control agents |
| CN111825585B (zh) | 2019-09-23 | 2021-12-14 | 山东康乔生物科技有限公司 | 一种含苄胺结构的芳基硫化物及其合成方法和应用 |
| CN112824402B (zh) * | 2019-11-21 | 2023-02-28 | 浙江省化工研究院有限公司 | 一类苯并咪唑类衍生物、其制备方法及应用 |
| AR121344A1 (es) | 2020-02-18 | 2022-05-11 | Pi Industries Ltd | Compuestos heterocíclicos fusionados y su uso como agentes para el control de plagas |
| US20230212163A1 (en) | 2020-04-21 | 2023-07-06 | Bayer Aktiengesellschaft | 2-(het)aryl-substituted condensed heterocyclic derivatives as pest control agents |
| CN116940236B (zh) * | 2021-02-07 | 2026-04-14 | 山东康乔生物科技有限公司 | 含有苄胺类杀螨剂的组合物及其应用 |
| EP4337661A1 (de) | 2021-05-12 | 2024-03-20 | Bayer Aktiengesellschaft | 2-(het)aryl-substituierte kondensierte heterocyclen-derivate als schädlingsbekämpfungsmittel |
| EP4405348B1 (en) | 2021-09-20 | 2026-02-25 | Basf Se | Heterocyclic compounds for the control of invertebrate pests |
| CN120882309A (zh) | 2023-03-14 | 2025-10-31 | 先正达农作物保护股份公司 | 对杀昆虫剂具有抗性的有害生物的控制 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI1015315B1 (pt) | 2009-04-28 | 2020-02-04 | Sumitomo Chemical Co | composto heterocíclico fundido, seu uso, composição e método de controlar um artrópode nocivo |
| TW201136919A (en) * | 2010-03-02 | 2011-11-01 | Merck Sharp & Amp Dohme Corp | Inhibitors of hepatitis C virus NS5B polymerase |
| JP5790440B2 (ja) | 2010-12-01 | 2015-10-07 | 住友化学株式会社 | ピリミジン化合物およびその有害生物防除用途 |
| EP3006429B1 (en) | 2010-12-24 | 2019-02-06 | Sumitomo Chemical Co., Ltd. | Fused heterocyclic compound and use for pest control thereof |
| TWI545119B (zh) | 2011-08-04 | 2016-08-11 | 住友化學股份有限公司 | 稠合雜環化合物及其在病蟲害防制上之用途 |
| JP6168055B2 (ja) | 2012-06-18 | 2017-07-26 | 住友化学株式会社 | 縮合複素環化合物 |
| UY35421A (es) | 2013-03-15 | 2014-10-31 | Nihon Nohyaku Co Ltd | Compuesto heterocíclico condensado o su sal, insecticida agrícola u hortícola que comprende el comp uesto y método de uso del insecticida |
| WO2014148451A1 (ja) | 2013-03-19 | 2014-09-25 | 日本農薬株式会社 | 縮合複素環化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法 |
| US9920050B2 (en) | 2013-07-01 | 2018-03-20 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and pest control use thereof |
| CA2917262A1 (en) * | 2013-07-02 | 2015-01-08 | Syngenta Participations Ag | Pesticidally active bi- or tricyclic heterocycles with sulfur containing substituents |
| EP2873668A1 (en) | 2013-11-13 | 2015-05-20 | Syngenta Participations AG. | Pesticidally active bicyclic heterocycles with sulphur containing substituents |
| CN105829324B (zh) | 2013-12-20 | 2018-12-14 | 先正达参股股份有限公司 | 具有含硫取代基的杀有害生物活性经取代的5,5-二环杂环 |
| MX388484B (es) * | 2014-02-17 | 2025-03-20 | Bayer Cropscience Ag | Derivados de heterociclos bicíclicos condensados sustituidos con 2-(het) arilo como agentes para combatir parásitos. |
| AR099677A1 (es) | 2014-03-07 | 2016-08-10 | Sumitomo Chemical Co | Compuesto heterocíclico fusionado y su uso para el control de plagas |
| WO2015198817A1 (en) | 2014-06-26 | 2015-12-30 | Sumitomo Chemical Company, Limited | Method for producing fused heterocyclic compound |
| WO2015198859A1 (ja) | 2014-06-26 | 2015-12-30 | 住友化学株式会社 | 縮合複素環化合物 |
| US9775353B2 (en) | 2014-07-08 | 2017-10-03 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| US9949483B2 (en) | 2014-08-07 | 2018-04-24 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| CN107074846B (zh) | 2014-08-12 | 2020-05-19 | 先正达参股股份有限公司 | 具有含硫取代基的杀有害生物活性杂环衍生物 |
| WO2016026848A1 (en) | 2014-08-21 | 2016-02-25 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| TW201625522A (zh) | 2014-09-12 | 2016-07-16 | Nihon Nohyaku Co Ltd | 咪唑嗒化合物或其鹽類及含有該化合物之農園藝用殺蟲劑及其使用方法 |
| WO2016041819A1 (en) | 2014-09-16 | 2016-03-24 | Syngenta Participations Ag | Pesticidally active tetracyclic derivatives with sulphur containing substituents |
| WO2016046071A1 (en) | 2014-09-25 | 2016-03-31 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| GB2535976C (en) | 2015-02-02 | 2017-03-29 | Drayson Tech (Europe) Ltd | Inverter for inductive power transfer |
| UY36548A (es) | 2015-02-05 | 2016-06-01 | Bayer Cropscience Ag | Derivados heterocíclicos condensados bicíclicos sustituidos por 2-(het)arilo como pesticidas |
-
2016
- 2016-09-23 KR KR1020187010246A patent/KR102629107B1/ko active Active
- 2016-09-23 PE PE2018000432A patent/PE20181094A1/es unknown
- 2016-09-23 EP EP16770499.8A patent/EP3356362B1/de active Active
- 2016-09-23 WO PCT/EP2016/072697 patent/WO2017055185A1/de not_active Ceased
- 2016-09-23 AU AU2016330299A patent/AU2016330299B2/en not_active Ceased
- 2016-09-23 CA CA2999790A patent/CA2999790A1/en not_active Abandoned
- 2016-09-23 BR BR112018006198-0A patent/BR112018006198B1/pt active IP Right Grant
- 2016-09-23 RU RU2018116054A patent/RU2018116054A/ru not_active Application Discontinuation
- 2016-09-23 JP JP2018515805A patent/JP6871917B2/ja active Active
- 2016-09-23 PH PH1/2018/500638A patent/PH12018500638B1/en unknown
- 2016-09-23 MX MX2018003761A patent/MX2018003761A/es unknown
- 2016-09-23 ES ES16770499T patent/ES2866911T3/es active Active
- 2016-09-23 US US15/763,168 patent/US10745398B2/en active Active
- 2016-09-23 CN CN201680069088.XA patent/CN108290886B/zh active Active
- 2016-09-26 TW TW105130960A patent/TWI720023B/zh not_active IP Right Cessation
- 2016-09-26 UY UY0001036918A patent/UY36918A/es not_active Application Discontinuation
- 2016-09-27 AR ARP160102944A patent/AR106165A1/es unknown
-
2018
- 2018-03-13 IL IL258089A patent/IL258089A/en unknown
- 2018-03-21 CL CL2018000741A patent/CL2018000741A1/es unknown
- 2018-03-27 CO CONC2018/0003427A patent/CO2018003427A2/es unknown
- 2018-04-26 ZA ZA2018/02797A patent/ZA201802797B/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2018529702A5 (enExample) | ||
| RU2018116054A (ru) | 2-(гет)арил-замещенные конденсированные гетероциклические производные в качестве средства для борьбы с вредителями | |
| JP2018536639A5 (enExample) | ||
| AU2009206468B2 (en) | Fungicidal heterocyclic compounds | |
| AU2009206522B2 (en) | Fungicidal amides | |
| EP3239137B1 (en) | (5r)-4,5-dihydro-isoxazole derivatives as well as 1-(2-chloroacetyl)-4-piperidine-carbonitrile and -carboxamide derivatives as intermediates in the preparation of e.g. 4-[4-[(5r)-4,5-dihydro-isoxazol-3-yl]-thiazol-2-yl]-piperidine derivatives as fungicides for crop protection | |
| US8618137B2 (en) | Fungicidal heterocyclic compounds | |
| AU2008316880B2 (en) | Fungicidal compounds and mixtures | |
| RU2018108149A (ru) | 2-(гет)арил-замещенные конденсированные гетероциклические производные в качестве средства для борьбы с вредителями | |
| CN101622245B (zh) | 杀真菌酰胺 | |
| AU2011204323B2 (en) | Fungicidal heterocyclic compounds | |
| WO2008091594A2 (en) | Fungicidal mixtures | |
| AU2006272551A1 (en) | Fungicidal carboxamides | |
| JP2012510520A5 (enExample) | ||
| JP2010523570A5 (enExample) | ||
| JP2010509190A5 (enExample) | ||
| EP2768829A1 (en) | Microbiocidal pyrazole derivatives | |
| RU2019104378A (ru) | Конденсированные бициклические гетероциклические производные в качестве средств для борьбы с вредителями | |
| RU2017105902A (ru) | Соединения для применения в дегельминтизации | |
| HRP20250562T1 (hr) | Spojevi i pripravci kao inhibitori sppl2a | |
| AU2014202324B2 (en) | Fungicidal compounds and mixtures | |
| US9604962B2 (en) | Fungicidal azocyclic amides |