JP2018525328A5 - - Google Patents
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- Publication number
- JP2018525328A5 JP2018525328A5 JP2017563077A JP2017563077A JP2018525328A5 JP 2018525328 A5 JP2018525328 A5 JP 2018525328A5 JP 2017563077 A JP2017563077 A JP 2017563077A JP 2017563077 A JP2017563077 A JP 2017563077A JP 2018525328 A5 JP2018525328 A5 JP 2018525328A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydrogen
- formula
- tautomer
- stereoisomer
- 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
- 229910052739 hydrogen Inorganic materials 0.000 claims description 34
- 239000001257 hydrogen Substances 0.000 claims description 34
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 18
- 229910052760 oxygen Inorganic materials 0.000 claims description 18
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 16
- 150000002431 hydrogen Chemical class 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 14
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 13
- 150000001204 N-oxides Chemical class 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 229910052736 halogen Inorganic materials 0.000 claims description 11
- 150000002367 halogens Chemical class 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 11
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- 239000001301 oxygen Substances 0.000 claims description 10
- 229910052717 sulfur Chemical group 0.000 claims description 10
- 239000011593 sulfur Chemical group 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 241000607479 Yersinia pestis Species 0.000 claims description 6
- -1 chloro, fluoro, methoxy Chemical group 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 241000282414 Homo sapiens Species 0.000 claims description 2
- 230000000895 acaricidal effect Effects 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 230000000855 fungicidal effect Effects 0.000 claims description 2
- 230000000749 insecticidal effect Effects 0.000 claims description 2
- 230000001069 nematicidal effect Effects 0.000 claims description 2
- 230000000361 pesticidal effect Effects 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 description 55
- 125000004093 cyano group Chemical group *C#N 0.000 description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
- 125000003545 alkoxy group Chemical group 0.000 description 11
- 125000005347 halocycloalkyl group Chemical group 0.000 description 10
- 125000001188 haloalkyl group Chemical group 0.000 description 9
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 7
- 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 description 7
- 125000001424 substituent group Chemical group 0.000 description 7
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 6
- 125000006310 cycloalkyl amino group Chemical group 0.000 description 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 5
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 description 5
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 description 5
- 125000000232 haloalkynyl group Chemical group 0.000 description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 description 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- 125000004663 dialkyl amino group Chemical group 0.000 description 4
- 125000002541 furyl group Chemical group 0.000 description 4
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- 125000003373 pyrazinyl group Chemical group 0.000 description 4
- 125000002098 pyridazinyl group Chemical group 0.000 description 4
- 125000004076 pyridyl group Chemical group 0.000 description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 description 4
- 125000001544 thienyl group Chemical group 0.000 description 4
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 description 3
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 description 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 125000000000 cycloalkoxy group Chemical group 0.000 description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- 125000006809 haloalkylaminocarbonyl group Chemical group 0.000 description 2
- 125000001072 heteroaryl group Chemical group 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- 125000000842 isoxazolyl group Chemical group 0.000 description 2
- 125000002971 oxazolyl group Chemical group 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- 125000000335 thiazolyl group Chemical group 0.000 description 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 1
- 125000005195 alkyl amino carbonyloxy group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- 125000005265 dialkylamine group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 125000000262 haloalkenyl group Chemical group 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15170862.5 | 2015-06-05 | ||
| EP15170862 | 2015-06-05 | ||
| PCT/EP2016/062335 WO2016193284A1 (en) | 2015-06-05 | 2016-06-01 | Pesticidally active oxime and hydrazone derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018525328A JP2018525328A (ja) | 2018-09-06 |
| JP2018525328A5 true JP2018525328A5 (enExample) | 2019-07-04 |
| JP6807876B2 JP6807876B2 (ja) | 2021-01-06 |
Family
ID=53284174
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017563077A Expired - Fee Related JP6807876B2 (ja) | 2015-06-05 | 2016-06-01 | 殺有害生物的に活性なオキシムおよびヒドラゾン誘導体 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10336691B2 (enExample) |
| EP (1) | EP3303285B1 (enExample) |
| JP (1) | JP6807876B2 (enExample) |
| CN (1) | CN107667090B (enExample) |
| BR (1) | BR112017025822B8 (enExample) |
| ES (1) | ES2788633T3 (enExample) |
| WO (1) | WO2016193284A1 (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105557698A (zh) * | 2014-10-16 | 2016-05-11 | 陕西美邦农药有限公司 | 一种含氟氧虫酰胺的高效杀虫组合物 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3525457B2 (ja) * | 1993-08-17 | 2004-05-10 | 日産化学工業株式会社 | セミカルバゾン誘導体及び有害生物防除剤 |
| JPH07215928A (ja) * | 1993-12-08 | 1995-08-15 | Nippon Nohyaku Co Ltd | ヒドラジン誘導体及び農園芸用殺虫剤 |
| US5631072A (en) | 1995-03-10 | 1997-05-20 | Avondale Incorporated | Method and means for increasing efficacy and wash durability of insecticide treated fabric |
| JP2000514815A (ja) * | 1996-07-24 | 2000-11-07 | ノバルティス アクチェンゲゼルシャフト | 農薬組成物 |
| EP1114030B1 (en) | 1998-09-15 | 2005-06-01 | Syngenta Participations AG | Pyridine ketones useful as herbicides |
| WO2003034823A1 (en) | 2001-10-25 | 2003-05-01 | Siamdutch Mosquito Netting Company Limited | Treatment of fabric materials with an insecticide |
| US20050132500A1 (en) | 2003-12-22 | 2005-06-23 | Basf Aktiengesellschaft | Composition for impregnation of fibers, fabrics and nettings imparting a protective activity against pests |
| DE102004023894A1 (de) | 2004-05-12 | 2005-12-08 | Basf Ag | Verfahren zur Behandlung von flexiblen Substraten |
| DE102005020889A1 (de) | 2005-05-04 | 2006-11-09 | Fritz Blanke Gmbh & Co.Kg | Verfahren zur antimikrobiellen Ausrüstung von textilen Flächengebilden |
| UA85488C2 (ru) | 2005-06-03 | 2009-01-26 | Басф Акциенгезелльшафт | Инсектицидная композиция, ее применение для нанесения на неживой материал, способ пропитки, пропитанный материал и способ покрытия |
| PT1984555T (pt) | 2006-02-03 | 2016-08-18 | Basf Se | Processo para o tratamento de substratos têxteis |
| WO2008151984A1 (en) | 2007-06-12 | 2008-12-18 | Basf Se | Aqueous formulation and process for the impregnation of non-living-materials imparting a protective activity against pests |
| NZ587143A (en) | 2008-02-12 | 2011-07-29 | Dow Agrosciences Llc | Pesticidal compositions |
| US20110030259A1 (en) | 2009-08-06 | 2011-02-10 | Castro Christopher R | Magazine and firearm with improved ammunition loading feature |
| UA108619C2 (xx) * | 2009-08-07 | 2015-05-25 | Пестицидні композиції | |
| CA2826146A1 (en) | 2011-02-07 | 2012-08-16 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| US8916183B2 (en) | 2012-02-02 | 2014-12-23 | Dow Agrosciences, Llc. | Pesticidal compositions and processes related thereto |
| CA2861353A1 (en) | 2012-02-02 | 2013-08-08 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| CN104602524A (zh) | 2012-07-09 | 2015-05-06 | 美国陶氏益农公司 | 杀虫组合物和与其相关的方法 |
-
2016
- 2016-06-01 WO PCT/EP2016/062335 patent/WO2016193284A1/en not_active Ceased
- 2016-06-01 CN CN201680032422.4A patent/CN107667090B/zh active Active
- 2016-06-01 JP JP2017563077A patent/JP6807876B2/ja not_active Expired - Fee Related
- 2016-06-01 ES ES16726113T patent/ES2788633T3/es active Active
- 2016-06-01 US US15/579,422 patent/US10336691B2/en active Active
- 2016-06-01 EP EP16726113.0A patent/EP3303285B1/en active Active
- 2016-06-01 BR BR112017025822A patent/BR112017025822B8/pt not_active IP Right Cessation
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