JP2018509391A5 - - Google Patents
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- JP2018509391A5 JP2018509391A5 JP2017541041A JP2017541041A JP2018509391A5 JP 2018509391 A5 JP2018509391 A5 JP 2018509391A5 JP 2017541041 A JP2017541041 A JP 2017541041A JP 2017541041 A JP2017541041 A JP 2017541041A JP 2018509391 A5 JP2018509391 A5 JP 2018509391A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- methyl
- alkoxy
- ethyl
- cycloalkyl
- 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.)
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 138
- -1 Cyano, nitro, hydroxy, amino, carboxy, carbamoyl Chemical group 0.000 claims description 74
- 229910052739 hydrogen Inorganic materials 0.000 claims description 70
- 239000001257 hydrogen Substances 0.000 claims description 69
- 150000002431 hydrogen Chemical class 0.000 claims description 53
- 125000001424 substituent group Chemical group 0.000 claims description 52
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 40
- 229910052736 halogen Inorganic materials 0.000 claims description 39
- 150000002367 halogens Chemical class 0.000 claims description 39
- 125000000623 heterocyclic group Chemical group 0.000 claims description 39
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 34
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 33
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 32
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 26
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 24
- 125000003118 aryl group Chemical group 0.000 claims description 23
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 22
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 22
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 22
- 229910052757 nitrogen Inorganic materials 0.000 claims description 22
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 21
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 21
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 20
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 20
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 19
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 19
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 18
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 15
- 229920006395 saturated elastomer Polymers 0.000 claims description 12
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 11
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 10
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 10
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 9
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 9
- 229910052717 sulfur Inorganic materials 0.000 claims description 9
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 8
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 8
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 8
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 8
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 8
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 claims description 8
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 8
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims description 8
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 8
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 8
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 6
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims description 6
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims description 5
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims description 4
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims description 4
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims description 4
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 4
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims description 4
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 4
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 2
- 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 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 71
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 58
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 47
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 41
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 35
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 29
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 26
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 24
- 150000001875 compounds Chemical class 0.000 claims 21
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 19
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 17
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 14
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 10
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 9
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims 9
- 125000006001 difluoroethyl group Chemical group 0.000 claims 7
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 7
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 7
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 7
- 125000006337 tetrafluoro ethyl group Chemical group 0.000 claims 7
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 7
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 6
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 5
- 125000003226 pyrazolyl group Chemical group 0.000 claims 5
- 125000004076 pyridyl group Chemical group 0.000 claims 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 239000000460 chlorine Substances 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Substances 0.000 claims 4
- 125000004760 (C1-C4) alkylsulfonylamino group Chemical group 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 3
- 241000607479 Yersinia pestis Species 0.000 claims 3
- 239000003905 agrochemical Substances 0.000 claims 3
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 3
- 238000009472 formulation Methods 0.000 claims 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 101150114085 soc-2 gene Proteins 0.000 claims 3
- 125000000335 thiazolyl group Chemical group 0.000 claims 3
- 125000004758 (C1-C4) alkoxyimino group Chemical group 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 125000004788 dichlorofluoromethoxy group Chemical group ClC(O*)(F)Cl 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 230000000361 pesticidal effect Effects 0.000 claims 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 2
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims 1
- JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 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
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15153948 | 2015-02-05 | ||
| EP15153948.3 | 2015-02-05 | ||
| EP15171696 | 2015-06-11 | ||
| EP15171696.6 | 2015-06-11 | ||
| PCT/EP2016/052105 WO2016124557A1 (de) | 2015-02-05 | 2016-02-02 | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018509391A JP2018509391A (ja) | 2018-04-05 |
| JP2018509391A5 true JP2018509391A5 (enExample) | 2019-03-14 |
| JP6738341B2 JP6738341B2 (ja) | 2020-08-12 |
Family
ID=55272500
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017541041A Active JP6738341B2 (ja) | 2015-02-05 | 2016-02-02 | 有害生物防除剤としての２−（ヘト）アリール置換された縮合二環式複素環誘導体 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US10654845B2 (enExample) |
| EP (1) | EP3253757B1 (enExample) |
| JP (1) | JP6738341B2 (enExample) |
| KR (1) | KR102524177B1 (enExample) |
| CN (1) | CN107428759B (enExample) |
| AU (1) | AU2016214496B2 (enExample) |
| BR (1) | BR112017016832B1 (enExample) |
| CA (1) | CA2975659A1 (enExample) |
| CL (1) | CL2017001977A1 (enExample) |
| CO (1) | CO2017007847A2 (enExample) |
| ES (1) | ES3029411T3 (enExample) |
| MX (1) | MX2017010124A (enExample) |
| PH (1) | PH12017501381A1 (enExample) |
| TW (1) | TWI725953B (enExample) |
| UY (1) | UY36547A (enExample) |
| WO (1) | WO2016124557A1 (enExample) |
| ZA (1) | ZA201706030B (enExample) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3331870B1 (de) * | 2015-08-07 | 2021-06-16 | Bayer CropScience Aktiengesellschaft | 2-(het)aryl-substituierte kondensierte heterocyclen-derivate als schädlingsbekämpfungsmittel |
| CA3000803C (en) * | 2015-10-13 | 2020-03-24 | Nihon Nohyaku Co., Ltd. | Oxime group-containing condensed heterocyclic compound or salt thereof, agricultural and horticultural insecticide comprising the compound, and method for using the insecticide |
| KR102666624B1 (ko) | 2015-10-26 | 2024-05-16 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 농약으로서의 융합된 비사이클릭 헤테로사이클 유도체 |
| WO2017093180A1 (de) | 2015-12-01 | 2017-06-08 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| CN108779118A (zh) | 2016-01-11 | 2018-11-09 | 拜耳作物科学股份公司 | 作为害虫防治剂的杂环衍生物 |
| WO2017144341A1 (de) | 2016-02-23 | 2017-08-31 | Bayer Cropscience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| WO2017174414A1 (de) | 2016-04-05 | 2017-10-12 | Bayer Cropscience Aktiengesellschaft | Naphthalin-derivate als schädlingsbekämpfungsmittel |
| EP3487860B1 (de) | 2016-07-19 | 2021-04-14 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| RU2019107162A (ru) | 2016-08-15 | 2020-09-15 | Байер Кропсайенс Акциенгезельшафт | Конденсированные бициклические гетероциклические производные в качестве средств для борьбы с вредителями |
| KR102420235B1 (ko) * | 2016-08-16 | 2022-07-12 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 3H-이미다졸[4,5-c]피리딘 유도체와 유기금속 아연-아민 염기의 반응에 의한 2-(3,6-디할로피리딘-2-일)-3H-이미다졸[4,5-c]피리딘 유도체 및 관련 화합물의 제조 방법 |
| MA46264A (fr) | 2016-09-19 | 2019-07-31 | Bayer Ag | Dérivés pyrazolo[1,5-a]pyridine et leur utilisation en tant qu'agents de lutte antiparasitaire |
| ES2877814T3 (es) * | 2016-10-06 | 2021-11-17 | Bayer Cropscience Ag | Derivados de heterociclos bicíclicos condensados sustituidos con 2-(het)arilo como pesticidas |
| WO2018065288A1 (de) | 2016-10-07 | 2018-04-12 | Bayer Cropscience Aktiengesellschaft | 2-[2-phenyl-1-(sulfonylmethyl)vinyl]-imidazo[4,5-b]pyridin-derivate und verwandte verbindungen als schädlingsbekämpfungsmittel im pflanzenschutz |
| CN117624038A (zh) | 2016-12-01 | 2024-03-01 | 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 |
| AU2017388692B2 (en) * | 2016-12-27 | 2020-12-03 | Nihon Nohyaku Co., Ltd. | Oxime group-containing condensed heterocyclic compound or salt thereof, agricultural and horticultural insecticide comprising the compound or the salt, and method for using the insecticide |
| MX2019008230A (es) | 2017-01-10 | 2019-10-24 | Bayer Ag | Derivados heterociclicos como agentes de control de plagas. |
| JP7101177B2 (ja) | 2017-01-10 | 2022-07-14 | バイエル・アクチエンゲゼルシヤフト | 有害生物防除剤としてのヘテロサイクレン誘導体 |
| WO2018138050A1 (de) | 2017-01-26 | 2018-08-02 | Bayer Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| 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 |
| 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 |
| WO2018202501A1 (de) * | 2017-05-02 | 2018-11-08 | Bayer Aktiengesellschaft | 2-(het)aryl-substituierte kondensierte heterocyclen-derivate als schädlingsbekämpfungsmittel |
| EP3619203A1 (en) * | 2017-05-02 | 2020-03-11 | Syngenta Participations AG | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2018202494A1 (de) * | 2017-05-02 | 2018-11-08 | Bayer Aktiengesellschaft | 2-(het)aryl-substituierte kondensierte heterocyclen-derivate als schädlingsbekämpfungsmittel |
| WO2019076778A1 (en) | 2017-10-16 | 2019-04-25 | Syngenta Participations Ag | HETEROCYCLIC DERIVATIVES HAVING PESTICIDAL ACTIVITY HAVING SUBSTITUENTS CONTAINING SULFUR AND SULFONIMIDAMIDES |
| MA51609A (fr) * | 2018-01-15 | 2021-04-21 | Syngenta Participations Ag | Dérivés hétérocycliques à activité pesticide comportant des substituants contenant du soufre |
| US11019821B2 (en) | 2018-02-21 | 2021-06-01 | Bayer Aktiengesellschaft | Fused bicyclic heterocycle derivatives as pesticides |
| KR20200130263A (ko) * | 2018-03-12 | 2020-11-18 | 닛뽕소다 가부시키가이샤 | 헤테로아릴피리미딘 화합물 및 유해 생물 방제제 |
| WO2019229088A1 (en) | 2018-05-30 | 2019-12-05 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2019229089A1 (en) | 2018-05-31 | 2019-12-05 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| MX2020013767A (es) | 2018-06-26 | 2021-03-02 | Bayer Ag | Derivados heterociclicos como plaguicidas. |
| KR20210133984A (ko) | 2019-02-26 | 2021-11-08 | 바이엘 악티엔게젤샤프트 | 해충 방제제로서의 축합된 비시클릭 헤테로시클릭 유도체 |
| CN113710669A (zh) | 2019-02-26 | 2021-11-26 | 拜耳公司 | 作为农药的稠合双环杂环衍生物 |
| WO2021009311A1 (en) | 2019-07-17 | 2021-01-21 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| CN115715290A (zh) | 2020-04-21 | 2023-02-24 | 拜耳公司 | 作为农药的2-(杂)芳基取代的稠杂环衍生物 |
| US20230247994A1 (en) | 2020-07-02 | 2023-08-10 | Bayer Aktiengesellschaft | Heterocyclene derivatives as pest control agents |
| EP4303214A4 (en) * | 2021-03-01 | 2025-02-19 | Nihon Nohyaku Co., Ltd. | CONDENSED HETEROCYCLIC COMPOUND HAVING A SULFONAMIDE GROUP OR SALT THEREOF, AGRICULTURAL/HORTICULTURAL PESTICIDE AND EXTERNAL OR INTERNAL ANIMAL PARASITE CONTAINING SAID COMPOUND OR SALT THEREOF, AND METHOD OF USING THE SAME |
| US20240294533A1 (en) | 2021-05-12 | 2024-09-05 | Bayer Aktiengesellschaft | 2-(het)aryl-substituted condensed heterocycle derivatives as pest control agents |
| CN113912533B (zh) * | 2021-11-23 | 2023-06-20 | 西安凯立新材料股份有限公司 | 一种制备3,6-二氯吡啶甲酸的方法 |
| 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 |
| WO2025026738A1 (en) | 2023-07-31 | 2025-02-06 | Bayer Aktiengesellschaft | 6-[5-(ethylsulfonyl)-1-methyl-1h-imidazol-4-yl]-7-methyl-3-(pentafluoroethyl)-7h-imidazo[4,5-c]pyridazine derivatives as pesticides |
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-
2016
- 2016-02-01 UY UY0001036547A patent/UY36547A/es not_active Application Discontinuation
- 2016-02-02 CN CN201680020466.5A patent/CN107428759B/zh active Active
- 2016-02-02 KR KR1020177024260A patent/KR102524177B1/ko active Active
- 2016-02-02 EP EP16702149.2A patent/EP3253757B1/de active Active
- 2016-02-02 US US15/547,871 patent/US10654845B2/en active Active
- 2016-02-02 WO PCT/EP2016/052105 patent/WO2016124557A1/de not_active Ceased
- 2016-02-02 AU AU2016214496A patent/AU2016214496B2/en active Active
- 2016-02-02 MX MX2017010124A patent/MX2017010124A/es unknown
- 2016-02-02 TW TW105103219A patent/TWI725953B/zh not_active IP Right Cessation
- 2016-02-02 CA CA2975659A patent/CA2975659A1/en not_active Abandoned
- 2016-02-02 BR BR112017016832-4A patent/BR112017016832B1/pt active IP Right Grant
- 2016-02-02 JP JP2017541041A patent/JP6738341B2/ja active Active
- 2016-02-02 ES ES16702149T patent/ES3029411T3/es active Active
-
2017
- 2017-08-01 PH PH12017501381A patent/PH12017501381A1/en unknown
- 2017-08-02 CO CONC2017/0007847A patent/CO2017007847A2/es unknown
- 2017-08-02 CL CL2017001977A patent/CL2017001977A1/es unknown
- 2017-09-05 ZA ZA2017/06030A patent/ZA201706030B/en unknown
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