JPWO2020201398A5 - - Google Patents
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- JPWO2020201398A5 JPWO2020201398A5 JP2021559151A JP2021559151A JPWO2020201398A5 JP WO2020201398 A5 JPWO2020201398 A5 JP WO2020201398A5 JP 2021559151 A JP2021559151 A JP 2021559151A JP 2021559151 A JP2021559151 A JP 2021559151A JP WO2020201398 A5 JPWO2020201398 A5 JP WO2020201398A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- halogen
- haloalkyl
- substituted
- alkoxy
- 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
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- 150000001875 compounds Chemical class 0.000 claims description 33
- 229910052736 halogen Inorganic materials 0.000 claims description 30
- 150000002367 halogens Chemical group 0.000 claims description 28
- 125000001188 haloalkyl group Chemical group 0.000 claims description 24
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 17
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims description 16
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 8
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical group C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 8
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 241000607479 Yersinia pestis Species 0.000 claims description 6
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 6
- 150000002431 hydrogen Chemical group 0.000 claims description 6
- -1 stereoisomers Chemical class 0.000 claims description 6
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 4
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims description 4
- 241000238631 Hexapoda Species 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 241000237852 Mollusca Species 0.000 claims description 4
- 241000244206 Nematoda Species 0.000 claims description 4
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Chemical group C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 4
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 4
- 125000004995 haloalkylthio group Chemical group 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical group C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 3
- 244000045947 parasite Species 0.000 claims description 3
- HCMJWOGOISXSDL-UHFFFAOYSA-N (2-isothiocyanato-1-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(CN=C=S)C1=CC=CC=C1 HCMJWOGOISXSDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 2
- 241000238876 Acari Species 0.000 claims description 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 2
- 241001465754 Metazoa Species 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- 230000000895 acaricidal effect Effects 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000000232 haloalkynyl group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 230000000749 insecticidal effect Effects 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004971 nitroalkyl group Chemical group 0.000 claims description 2
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical group ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002013 molluscicidal effect Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP19167690.7 | 2019-04-05 | ||
| EP19167690 | 2019-04-05 | ||
| EP19196235 | 2019-09-09 | ||
| EP19196235.6 | 2019-09-09 | ||
| EP20151656.4 | 2020-01-14 | ||
| EP20151656 | 2020-01-14 | ||
| PCT/EP2020/059338 WO2020201398A1 (en) | 2019-04-05 | 2020-04-02 | Pesticidally active diazine-amide compounds |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| JP2022527548A JP2022527548A (ja) | 2022-06-02 |
| JP2022527548A5 JP2022527548A5 (https=) | 2023-04-07 |
| JPWO2020201398A5 true JPWO2020201398A5 (https=) | 2023-04-07 |
| JP7611848B2 JP7611848B2 (ja) | 2025-01-10 |
Family
ID=70058398
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021559151A Active JP7611848B2 (ja) | 2019-04-05 | 2020-04-02 | 殺有害生物的に活性なジアジン－アミド化合物 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US12527325B2 (https=) |
| EP (1) | EP3947359A1 (https=) |
| JP (1) | JP7611848B2 (https=) |
| KR (1) | KR20210149113A (https=) |
| CN (1) | CN113661165B (https=) |
| AU (1) | AU2020255265A1 (https=) |
| BR (1) | BR112021019987A2 (https=) |
| CA (1) | CA3131479A1 (https=) |
| CO (1) | CO2021013183A2 (https=) |
| IL (1) | IL286871A (https=) |
| JO (1) | JOP20210272A1 (https=) |
| MA (1) | MA55500A (https=) |
| MX (1) | MX2021012162A (https=) |
| PE (1) | PE20220171A1 (https=) |
| PY (1) | PY2018189A (https=) |
| TW (1) | TW202104205A (https=) |
| UY (1) | UY38649A (https=) |
| WO (1) | WO2020201398A1 (https=) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI853009B (zh) * | 2019-03-29 | 2024-08-21 | 瑞士商先正達農作物保護公司 | 殺有害生物活性之二-醯胺化合物 |
| TW202128650A (zh) * | 2019-10-11 | 2021-08-01 | 德商拜耳動物保健有限公司 | 作為殺蟲劑之新穎的雜芳基取代之吡𠯤衍生物 |
| EP4077322A1 (en) | 2019-12-18 | 2022-10-26 | Intervet International B.V. | Anthelmintic compounds comprising azaindoles structure |
| AU2020406093A1 (en) | 2019-12-18 | 2022-06-16 | Intervet International B.V. | Anthelmintic compounds comprising a quinoline structure |
| WO2021122645A1 (en) * | 2019-12-20 | 2021-06-24 | Syngenta Crop Protection Ag | Pesticidally active azole-amide compounds |
| EP3929189A1 (en) * | 2020-06-25 | 2021-12-29 | Bayer Animal Health GmbH | Novel heteroaryl-substituted pyrazine derivatives as pesticides |
| WO2022101265A1 (en) | 2020-11-13 | 2022-05-19 | Syngenta Crop Protection Ag | Pesticidally active fused bicyclic heteroaromatic compounds |
| US20240043446A1 (en) | 2020-12-11 | 2024-02-08 | Intervet Inc. | Anthelmintic compounds comprising a thienopyridine structure |
| WO2022233777A1 (en) | 2021-05-06 | 2022-11-10 | Bayer Aktiengesellschaft | Alkylamide substituted, annulated imidazoles and use thereof as insecticides |
| JP2024524883A (ja) * | 2021-06-09 | 2024-07-09 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺有害生物的に活性なジアジン－アミド化合物 |
| AU2022318251A1 (en) | 2021-07-29 | 2024-01-25 | Syngenta Crop Protection Ag | Pesticidally active fused bicyclic heteroaromatic compounds |
| US20250107528A1 (en) | 2021-08-23 | 2025-04-03 | Basf Se | Pyrazine compounds for the control of invertebrate pests |
| EP4140986A1 (en) | 2021-08-23 | 2023-03-01 | Basf Se | Pyrazine compounds for the control of invertebrate pests |
| WO2023025682A1 (en) | 2021-08-25 | 2023-03-02 | Bayer Aktiengesellschaft | Novel pyrazinyl-triazole compounds as pesticides |
| WO2023104714A1 (en) | 2021-12-10 | 2023-06-15 | Syngenta Crop Protection Ag | Pesticidally active pyridazinone compounds |
| WO2024110554A1 (en) | 2022-11-23 | 2024-05-30 | Syngenta Crop Protection Ag | N-[(1 -[2-[6-(pyridazin-3-yl]-1,2,4-triazol-3-yl]ethyl]-quinazolin-4-amine and n-[1-[3-(6-(pyridazin-3-yl)pyrazin-2-yl]ethyl]-8-quinazolin-4-amine derivatives as pesticides |
| WO2024133551A1 (en) | 2022-12-21 | 2024-06-27 | Syngenta Crop Protection Ag | Pesticidally active pyridazine compounds |
| WO2025186065A1 (en) | 2024-03-05 | 2025-09-12 | Bayer Aktiengesellschaft | Heteroaryl-substituted (aza)quinoxaline derivatives as pesticides |
| WO2025224076A1 (de) | 2024-04-23 | 2025-10-30 | Bayer Aktiengesellschaft | Substituierte arylpyrazine sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| WO2025257242A1 (de) | 2024-06-14 | 2025-12-18 | Bayer Aktiengesellschaft | Heterocyclyl-substituierte aryl- und heteroarylpyrazine sowie deren salze und ihre verwendung als herbizide wirkstoffe |
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| BR112015014191B1 (pt) | 2012-12-19 | 2019-08-27 | Bayer Cropscience Ag | indanil carboxamidas difluorometilnicotínicas |
| SI3129355T1 (sl) | 2014-04-11 | 2019-03-29 | Syngenta Participations Ag | Fungicidni derivati N'-(2-metil-6-(2-alkoksi-etoksi)-3-piridil)-N-alkil-formamida za uporabo v poljedelstvu |
| HUE058009T2 (hu) | 2014-12-09 | 2022-06-28 | Bayer Ag | 1,3-Tiazol-2-il szubsztituált benzamid-származékok |
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| EA035584B1 (ru) | 2015-08-12 | 2020-07-10 | Зингента Партисипейшнс Аг | Микробиоцидные гетеробициклические производные |
| KR20180037267A (ko) | 2015-08-14 | 2018-04-11 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 트리아졸 유도체, 그의 중간체 및 살진균제로서의 그의 용도 |
| HUE050030T2 (hu) | 2015-10-02 | 2020-11-30 | Syngenta Participations Ag | Mikrobiocid oxadiazol-származékok |
| MX2018003845A (es) | 2015-10-02 | 2018-06-18 | Syngenta Participations Ag | Derivados de oxadiazol microbicidas. |
| CN108289448B (zh) | 2015-12-02 | 2021-10-22 | 先正达参股股份有限公司 | 杀微生物的噁二唑衍生物 |
| UY37062A (es) | 2016-01-08 | 2017-08-31 | Syngenta Participations Ag | Derivados de aryl oxadiazol fungicidas |
| CA3015449C (en) | 2016-03-10 | 2021-11-23 | Syngenta Participations Ag | Microbiocidal quinoline (thio)carboxamide derivatives |
| TWI696615B (zh) * | 2016-05-05 | 2020-06-21 | 瑞士商伊蘭科動物健康公司 | 雜芳基-1,2,4-三唑及雜芳基-三唑化合物 |
| AR108745A1 (es) | 2016-06-21 | 2018-09-19 | Syngenta Participations Ag | Derivados de oxadiazol microbiocidas |
| JP7077313B2 (ja) | 2016-10-06 | 2022-05-30 | シンジェンタ パーティシペーションズ アーゲー | 殺微生物オキサジアゾール誘導体 |
| WO2018153707A1 (en) | 2017-02-22 | 2018-08-30 | Basf Se | Crystalline forms of a strobilurin type compound for combating phytopathogenic fungi |
| UY37623A (es) | 2017-03-03 | 2018-09-28 | Syngenta Participations Ag | Derivados de oxadiazol tiofeno fungicidas |
| EP3618629A1 (en) | 2017-05-02 | 2020-03-11 | Basf Se | Fungicidal mixture comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles |
| WO2018228896A1 (en) | 2017-06-14 | 2018-12-20 | Syngenta Participations Ag | Fungicidal compositions |
| EP3720846A1 (en) | 2017-12-04 | 2020-10-14 | Syngenta Participations AG | Microbiocidal phenylamidine derivatives |
| PY1980182A (es) | 2018-10-02 | 2020-08-21 | Syngenta Participations Ag | Compuestos de benceno y azina-amida activos como plaguicidas |
-
2020
- 2020-04-02 JP JP2021559151A patent/JP7611848B2/ja active Active
- 2020-04-02 CN CN202080027187.8A patent/CN113661165B/zh active Active
- 2020-04-02 MX MX2021012162A patent/MX2021012162A/es unknown
- 2020-04-02 EP EP20715878.3A patent/EP3947359A1/en active Pending
- 2020-04-02 CA CA3131479A patent/CA3131479A1/en active Pending
- 2020-04-02 MA MA055500A patent/MA55500A/fr unknown
- 2020-04-02 PE PE2021001670A patent/PE20220171A1/es unknown
- 2020-04-02 WO PCT/EP2020/059338 patent/WO2020201398A1/en not_active Ceased
- 2020-04-02 AU AU2020255265A patent/AU2020255265A1/en not_active Abandoned
- 2020-04-02 BR BR112021019987A patent/BR112021019987A2/pt active IP Right Grant
- 2020-04-02 US US17/594,118 patent/US12527325B2/en active Active
- 2020-04-02 KR KR1020217035474A patent/KR20210149113A/ko not_active Withdrawn
- 2020-04-03 UY UY0001038649A patent/UY38649A/es not_active Application Discontinuation
- 2020-04-06 TW TW109111495A patent/TW202104205A/zh unknown
- 2020-05-05 PY PY202002018189A patent/PY2018189A/es unknown
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2021
- 2021-09-30 CO CONC2021/0013183A patent/CO2021013183A2/es unknown
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- 2021-10-04 JO JOP/2021/0272A patent/JOP20210272A1/ar unknown
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