JPWO2020182649A5 - - Google Patents
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- JPWO2020182649A5 JPWO2020182649A5 JP2021553291A JP2021553291A JPWO2020182649A5 JP WO2020182649 A5 JPWO2020182649 A5 JP WO2020182649A5 JP 2021553291 A JP2021553291 A JP 2021553291A JP 2021553291 A JP2021553291 A JP 2021553291A JP WO2020182649 A5 JPWO2020182649 A5 JP WO2020182649A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- compound according
- cycloalkyl
- halogen
- haloalkyl
- 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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- 150000001875 compounds Chemical class 0.000 claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims description 33
- 229910052736 halogen Inorganic materials 0.000 claims description 21
- 150000002367 halogens Chemical class 0.000 claims description 19
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 16
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 14
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 6
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims description 6
- 241000607479 Yersinia pestis Species 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 5
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 4
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 4
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 4
- 241000238631 Hexapoda Species 0.000 claims description 4
- 241000237852 Mollusca Species 0.000 claims description 4
- 150000001204 N-oxides Chemical class 0.000 claims description 4
- 241000244206 Nematoda Species 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
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 241000238876 Acari Species 0.000 claims description 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 3
- 125000004770 (C1-C4) haloalkylsulfanyl group Chemical group 0.000 claims description 2
- 125000006660 (C3-C4) halocycloalkyl group Chemical group 0.000 claims description 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- -1 2-pyrimidyl 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
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 2
- 230000000895 acaricidal effect Effects 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 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
- SXZIXHOMFPUIRK-UHFFFAOYSA-N diphenylmethanimine Chemical compound C=1C=CC=CC=1C(=N)C1=CC=CC=C1 SXZIXHOMFPUIRK-UHFFFAOYSA-N 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
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 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
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 244000045947 parasite Species 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- PQDJYEQOELDLCP-UHFFFAOYSA-N trimethylsilane Chemical compound C[SiH](C)C PQDJYEQOELDLCP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 231100000167 toxic agent Toxicity 0.000 claims 1
- 239000003440 toxic substance Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000004966 cyanoalkyl group Chemical group 0.000 description 2
- 125000004995 haloalkylthio group Chemical group 0.000 description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000004428 fluoroalkoxy group Chemical group 0.000 description 1
- 230000002013 molluscicidal effect Effects 0.000 description 1
- 125000004971 nitroalkyl group Chemical group 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP19161558 | 2019-03-08 | ||
| EP19161558.2 | 2019-03-08 | ||
| PCT/EP2020/055989 WO2020182649A1 (en) | 2019-03-08 | 2020-03-06 | Pesticidally active azole-amide compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022523434A JP2022523434A (ja) | 2022-04-22 |
| JP2022523434A5 JP2022523434A5 (https=) | 2023-03-10 |
| JPWO2020182649A5 true JPWO2020182649A5 (https=) | 2023-03-10 |
Family
ID=65729184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021553291A Ceased JP2022523434A (ja) | 2019-03-08 | 2020-03-06 | 殺有害生物的に活性なアゾール－アミド化合物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20220167618A1 (https=) |
| EP (1) | EP3935053B1 (https=) |
| JP (1) | JP2022523434A (https=) |
| CN (1) | CN113544125A (https=) |
| BR (1) | BR112021017646A2 (https=) |
| ES (1) | ES2953140T3 (https=) |
| WO (1) | WO2020182649A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UY38184A (es) | 2018-04-17 | 2019-10-31 | Bayer Ag | Compuestos heteroarilo-triazol y heteroarilo-tetrazol novedosos como plaguicidas |
| BR112021018501A2 (pt) * | 2019-03-20 | 2021-11-30 | Syngenta Crop Protection Ag | Compostos de azolamida ativos em termos pesticidas |
| JP7689109B2 (ja) | 2019-07-23 | 2025-06-05 | バイエル・アクチエンゲゼルシヤフト | 農薬としての新規ヘテロアリール－トリアゾール化合物 |
| PH12022550862A1 (en) * | 2019-10-09 | 2023-04-24 | Bayer Ag | Novel heteroaryl-triazole compounds as pesticides |
| TW202134226A (zh) | 2019-11-18 | 2021-09-16 | 德商拜耳廠股份有限公司 | 作為殺蟲劑之新穎雜芳基-三唑化合物 |
| TW202136248A (zh) | 2019-11-25 | 2021-10-01 | 德商拜耳廠股份有限公司 | 作為殺蟲劑之新穎雜芳基-三唑化合物 |
| WO2021122645A1 (en) * | 2019-12-20 | 2021-06-24 | Syngenta Crop Protection Ag | Pesticidally active azole-amide compounds |
| EP4107151A1 (en) | 2020-02-18 | 2022-12-28 | Bayer Aktiengesellschaft | Heteroaryl-triazole compounds as pesticides |
| TWI907288B (zh) | 2020-05-06 | 2025-12-01 | 德商拜耳廠股份有限公司 | 作為殺蟲劑之新穎雜芳基三唑化合物 |
| WO2022233777A1 (en) | 2021-05-06 | 2022-11-10 | Bayer Aktiengesellschaft | Alkylamide substituted, annulated imidazoles and use thereof as insecticides |
| WO2023025682A1 (en) | 2021-08-25 | 2023-03-02 | Bayer Aktiengesellschaft | Novel pyrazinyl-triazole compounds as pesticides |
| AU2022361189B2 (en) | 2021-10-08 | 2025-01-23 | Nihon Nohyaku Co., Ltd. | Pyrimidinyl triazole compound or salt thereof, pest control agent containing said compound as active ingredient, and pest control method |
| WO2025186065A1 (en) | 2024-03-05 | 2025-09-12 | Bayer Aktiengesellschaft | Heteroaryl-substituted (aza)quinoxaline derivatives as pesticides |
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| US10738045B2 (en) * | 2015-11-23 | 2020-08-11 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur and cyclopropyl containing substituents |
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| 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 |
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| CA3015449C (en) | 2016-03-10 | 2021-11-23 | Syngenta Participations Ag | Microbiocidal quinoline (thio)carboxamide derivatives |
| JP6911052B2 (ja) | 2016-05-03 | 2021-07-28 | バイエル ファーマ アクチエンゲゼルシャフト | オキソアルキル置換フェニルトリアゾール誘導体およびその使用 |
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| 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 |
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| 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 |
| JP2021522181A (ja) * | 2018-04-20 | 2021-08-30 | バイエル・アクチエンゲゼルシヤフト | 殺有害生物剤としてのヘテロアリール−トリアゾール化合物及びヘテロアリール−テトラゾール化合物 |
| MX2020011275A (es) * | 2018-04-25 | 2020-11-13 | Bayer Ag | Novedosos compuestos de heteroaril-triazol y hetroaril[-]tetrazol como plaguicidas. |
| PY1986700A (es) * | 2018-10-19 | 2020-08-28 | Syngenta Participations Ag | Compuestos de azol-amida pesticidamente activos |
| EP3935056A1 (en) * | 2019-03-08 | 2022-01-12 | Syngenta Crop Protection AG | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| 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 |
-
2020
- 2020-03-06 WO PCT/EP2020/055989 patent/WO2020182649A1/en not_active Ceased
- 2020-03-06 BR BR112021017646A patent/BR112021017646A2/pt active Search and Examination
- 2020-03-06 JP JP2021553291A patent/JP2022523434A/ja not_active Ceased
- 2020-03-06 EP EP20708497.1A patent/EP3935053B1/en active Active
- 2020-03-06 CN CN202080019251.8A patent/CN113544125A/zh active Pending
- 2020-03-06 US US17/437,264 patent/US20220167618A1/en not_active Abandoned
- 2020-03-06 ES ES20708497T patent/ES2953140T3/es active Active
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