RU2765282C2 - Пестицидно активные гетероциклические производные с серосодержащими заместителями - Google Patents
Пестицидно активные гетероциклические производные с серосодержащими заместителями Download PDFInfo
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- RU2765282C2 RU2765282C2 RU2017125267A RU2017125267A RU2765282C2 RU 2765282 C2 RU2765282 C2 RU 2765282C2 RU 2017125267 A RU2017125267 A RU 2017125267A RU 2017125267 A RU2017125267 A RU 2017125267A RU 2765282 C2 RU2765282 C2 RU 2765282C2
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
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- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cultivation Of Plants (AREA)
- Catching Or Destruction (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
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| EP14198495.5 | 2014-12-17 | ||
| EP14198495 | 2014-12-17 | ||
| PCT/EP2015/079188 WO2016096584A1 (en) | 2014-12-17 | 2015-12-10 | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
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| RU2017125267A RU2017125267A (ru) | 2019-01-17 |
| RU2017125267A3 RU2017125267A3 (https=) | 2019-05-30 |
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| CN (2) | CN110526911B (https=) |
| AU (1) | AU2015366548B2 (https=) |
| BR (1) | BR112017012638B1 (https=) |
| CA (1) | CA2969600C (https=) |
| CL (1) | CL2017001533A1 (https=) |
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| US10005775B2 (en) * | 2014-08-12 | 2018-06-26 | Syngenta Participations, Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| UA121319C2 (uk) * | 2014-11-07 | 2020-05-12 | Сінгента Партісіпейшнс Аг | Пестицидно активні поліциклічні похідні з сірковмісними замісниками |
| CN107001352B (zh) * | 2014-12-01 | 2021-06-04 | 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酰胺杂环衍生物 |
| US10323030B2 (en) * | 2014-12-17 | 2019-06-18 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| TWI696612B (zh) | 2015-01-29 | 2020-06-21 | 日商日本農藥股份有限公司 | 具有環烷基吡啶基的稠合雜環化合物或其鹽類及含有該化合物的農園藝用殺蟲劑以及其使用方法 |
| KR102435080B1 (ko) * | 2016-07-19 | 2022-08-22 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 해충 방제제로서의 축합 바이시클릭 헤테로사이클 유도체 |
| EP3523299B1 (de) | 2016-10-06 | 2021-04-14 | Bayer CropScience Aktiengesellschaft | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlings-bekämpfungsmittel |
| 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 |
| EP3554242A1 (en) | 2016-12-15 | 2019-10-23 | Syngenta Participations AG | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| UA123249C2 (uk) | 2016-12-27 | 2021-03-03 | Ніхон Нохіяку Ко., Лтд. | Сполука 4н-піролопіридину або її сіль, сільськогосподарський і садівницький інсектицид, який включає зазначену сполуку або її сіль, і спосіб застосування інсектициду |
| AU2018208422B2 (en) | 2017-01-10 | 2021-11-11 | Bayer Aktiengesellschaft | Heterocyclene derivatives as pest control agents |
| MX2019008229A (es) | 2017-01-10 | 2019-10-24 | Bayer Ag | Derivados heterociclicos como agentes de control de plagas. |
| TWI793104B (zh) | 2017-02-21 | 2023-02-21 | 瑞士商先正達合夥公司 | 具有含硫取代基的殺有害生物活性雜環衍生物 |
| US20200216441A1 (en) | 2017-04-25 | 2020-07-09 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| WO2018215304A1 (en) | 2017-05-22 | 2018-11-29 | Syngenta Participations Ag | Tetracyclic pyridazine sulphur containing compounds and their use as pesticides |
| JPWO2019059244A1 (ja) * | 2017-09-21 | 2020-11-05 | 日本農薬株式会社 | シクロプロピルピリジル基を有するベンゾイミダゾール化合物又はその塩類、及びそれらの化合物を含有する農園芸用殺虫剤並びにその使用方法 |
| CA3102190A1 (en) | 2018-06-06 | 2019-12-12 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfoximine containing substituents |
| JP7353310B2 (ja) | 2018-06-26 | 2023-09-29 | 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 |
| EP3835301B1 (en) | 2018-07-10 | 2024-10-09 | Nihon Nohyaku Co., Ltd. | Benzimidazole compound having alkylenedioxy group which may be halogenated or salt thereof, agricultural and horticultural pesticide containing said compound, and method of using same |
| TW202035404A (zh) | 2018-10-24 | 2020-10-01 | 瑞士商先正達農作物保護公司 | 具有含亞碸亞胺的取代基之殺有害生物活性雜環衍生物 |
| PL3878842T3 (pl) * | 2018-10-29 | 2025-03-31 | Nippon Soda Co., Ltd. | Związki (hetero)aryloimidazolu i środki do zwalczania szkodliwych organizmów |
| JP7535532B2 (ja) | 2019-02-26 | 2024-08-16 | 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縮合二環式複素環式誘導体 |
| WO2020175491A1 (ja) | 2019-02-26 | 2020-09-03 | 日本曹達株式会社 | ピリジン ｎ－オキサイド化合物および有害生物防除剤 |
| TW202120479A (zh) | 2019-11-27 | 2021-06-01 | 瑞士商先正達農作物保護公司 | 用於製備具有3-含硫取代基的5-氯-吡啶-2-羧酸及羧酸酯之方法 |
| TW202134214A (zh) | 2020-03-04 | 2021-09-16 | 瑞士商先正達農作物保護公司 | 用於製備具有3-含硫取代基的5-氯-吡啶-2-甲酸醯胺以及甲酸鹽之方法 |
| US20230247994A1 (en) | 2020-07-02 | 2023-08-10 | Bayer Aktiengesellschaft | Heterocyclene derivatives as pest control agents |
| WO2022043468A1 (en) | 2020-08-26 | 2022-03-03 | Syngenta Crop Protection Ag | Process for the preparation of 2,2-difluoro-1,3-benzodioxole derivatives with sulfur containing substituents |
| BR112023025278A2 (pt) | 2021-06-02 | 2024-02-27 | Syngenta Crop Protection Ag | Derivados heterocíclicos com substituintes contendo sulfoximina ativos em termos pesticidas |
| EP4680028A1 (en) | 2023-03-14 | 2026-01-21 | Syngenta Crop Protection AG | Control of pests resistant to insecticides |
| 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 |
| WO2026037853A1 (en) | 2024-08-14 | 2026-02-19 | Basf Se | Benzoxazole derivatives as pesticidal compounds |
| WO2026041702A1 (en) | 2024-08-21 | 2026-02-26 | Basf Se | Benzoxazole derivatives as pesticidal compounds |
| WO2026046760A1 (en) | 2024-08-29 | 2026-03-05 | Basf Se | Pesticidal mixtures comprising an ethylsulfone compound |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2036195C1 (ru) * | 1991-06-03 | 1995-05-27 | Сумитомо Кемикал Компани, Лимитед | Производные бензимидазола и промежуточные соединения для их получения |
| WO2010125985A1 (en) * | 2009-04-28 | 2010-11-04 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use thereof |
| WO2011040629A1 (en) * | 2009-09-30 | 2011-04-07 | Sumitomo Chemical Company, Limited | Composition and method for controlling arthropod pests |
| WO2012086848A1 (en) * | 2010-12-24 | 2012-06-28 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use for pest control thereof |
| WO2013018928A1 (en) * | 2011-08-04 | 2013-02-07 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use thereof for pest control |
| WO2013180194A1 (ja) * | 2012-05-30 | 2013-12-05 | 住友化学株式会社 | 縮合複素環化合物 |
| WO2014119494A1 (ja) * | 2013-01-31 | 2014-08-07 | 住友化学株式会社 | 有害生物防除組成物及び有害生物の防除方法 |
| JP2014208695A (ja) * | 2014-07-04 | 2014-11-06 | 住友化学株式会社 | 有害生物防除組成物およびその用途 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES8401486A1 (es) * | 1981-11-10 | 1983-12-01 | Wellcome Found | Un procedimiento para la preparacion de nuevos derivados de imidazo (4,5-c)piridina. |
| US4772600A (en) * | 1986-06-09 | 1988-09-20 | A. H. Robins Company, Inc. | Fused imidazoheterocyclic compounds and pharmaceutical compositions |
| WO2012033548A2 (en) * | 2010-09-07 | 2012-03-15 | E. I. Du Pont De Nemours And Company | Herbicidal bis-nitrogen-containing oxo and sulfono heterocycles |
| 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 |
| WO2015121136A1 (de) * | 2014-02-17 | 2015-08-20 | Bayer Cropscience Ag | 2-(het)aryl-substituierte kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| EP3194394B1 (en) * | 2014-09-16 | 2019-01-09 | Syngenta Participations AG | Pesticidally active tetracyclic derivatives with sulphur containing substituents |
| US10323030B2 (en) * | 2014-12-17 | 2019-06-18 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
-
2015
- 2015-12-10 US US15/536,820 patent/US10323030B2/en active Active
- 2015-12-10 BR BR112017012638-9A patent/BR112017012638B1/pt active IP Right Grant
- 2015-12-10 HU HUE15807678A patent/HUE050562T2/hu unknown
- 2015-12-10 CN CN201910793016.5A patent/CN110526911B/zh active Active
- 2015-12-10 JP JP2017532702A patent/JP6675404B2/ja active Active
- 2015-12-10 KR KR1020177016823A patent/KR102540827B1/ko active Active
- 2015-12-10 PL PL15807678T patent/PL3233851T3/pl unknown
- 2015-12-10 UA UAA201707453A patent/UA122781C2/uk unknown
- 2015-12-10 WO PCT/EP2015/079188 patent/WO2016096584A1/en not_active Ceased
- 2015-12-10 RS RS20201031A patent/RS60709B1/sr unknown
- 2015-12-10 AU AU2015366548A patent/AU2015366548B2/en active Active
- 2015-12-10 CA CA2969600A patent/CA2969600C/en active Active
- 2015-12-10 ES ES15807678T patent/ES2813952T3/es active Active
- 2015-12-10 SI SI201531332T patent/SI3233851T1/sl unknown
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- 2015-12-10 RU RU2017125267A patent/RU2765282C2/ru active
- 2015-12-10 MX MX2017007900A patent/MX394806B/es unknown
- 2015-12-10 PT PT158076786T patent/PT3233851T/pt unknown
- 2015-12-10 DK DK15807678.6T patent/DK3233851T3/da active
- 2015-12-10 LT LTEP15807678.6T patent/LT3233851T/lt unknown
- 2015-12-10 EP EP15807678.6A patent/EP3233851B1/en active Active
- 2015-12-10 CN CN201580068692.6A patent/CN107001365B/zh active Active
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-
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- 2017-06-01 PH PH12017501013A patent/PH12017501013A1/en unknown
- 2017-06-12 CO CONC2017/0005790A patent/CO2017005790A2/es unknown
- 2017-06-14 CL CL2017001533A patent/CL2017001533A1/es unknown
-
2019
- 2019-06-17 US US16/443,596 patent/US11072608B2/en active Active
-
2021
- 2021-06-17 US US17/350,374 patent/US20210317119A1/en active Pending
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2036195C1 (ru) * | 1991-06-03 | 1995-05-27 | Сумитомо Кемикал Компани, Лимитед | Производные бензимидазола и промежуточные соединения для их получения |
| WO2010125985A1 (en) * | 2009-04-28 | 2010-11-04 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use thereof |
| WO2011040629A1 (en) * | 2009-09-30 | 2011-04-07 | Sumitomo Chemical Company, Limited | Composition and method for controlling arthropod pests |
| WO2012086848A1 (en) * | 2010-12-24 | 2012-06-28 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use for pest control thereof |
| WO2013018928A1 (en) * | 2011-08-04 | 2013-02-07 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use thereof for pest control |
| WO2013180194A1 (ja) * | 2012-05-30 | 2013-12-05 | 住友化学株式会社 | 縮合複素環化合物 |
| WO2014119494A1 (ja) * | 2013-01-31 | 2014-08-07 | 住友化学株式会社 | 有害生物防除組成物及び有害生物の防除方法 |
| JP2014208695A (ja) * | 2014-07-04 | 2014-11-06 | 住友化学株式会社 | 有害生物防除組成物およびその用途 |
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