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 (https=) | 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 (https=) |
| EP (1) | EP3303285B1 (https=) |
| JP (1) | JP6807876B2 (https=) |
| CN (1) | CN107667090B (https=) |
| BR (1) | BR112017025822B8 (https=) |
| ES (1) | ES2788633T3 (https=) |
| WO (1) | WO2016193284A1 (https=) |
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 |
| TR199900124T2 (xx) * | 1996-07-24 | 1999-03-22 | Novartis Ag | Ha�ere �ld�r�c� bile�imler |
| BR9913745B1 (pt) | 1998-09-15 | 2011-05-31 | cetonas de piridina, composição herbicida e inibidora do crescimento de plantas, seu uso, método para controle de crescimento de plantas indesejáveis, bem como método para inibir o crescimento de plantas. | |
| 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 |
| AP2007004257A0 (en) | 2005-06-03 | 2007-12-31 | Basf Ag | Composition for impregnation of fibres fabrics andnettings imparting a protective activity against pests |
| ES2586569T3 (es) | 2006-02-03 | 2016-10-17 | Basf Se | Procedimiento para el tratamiento de sustratos textiles |
| JP5230731B2 (ja) | 2007-06-12 | 2013-07-10 | ビーエーエスエフ ソシエタス・ヨーロピア | 害虫からの保護活性を付与するための非生物材料への含浸用水性製剤及び含浸方法 |
| CN101998963B (zh) | 2008-02-12 | 2014-09-24 | 陶氏益农公司 | 杀虫组合物 |
| 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 | |
| ES2656040T3 (es) | 2011-02-07 | 2018-02-22 | Dow Agrosciences Llc | Composiciones pesticidas y procedimientos relacionados con las mismas |
| NZ627331A (en) | 2012-02-02 | 2016-03-31 | 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 |
| WO2014011429A1 (en) | 2012-07-09 | 2014-01-16 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
-
2016
- 2016-06-01 WO PCT/EP2016/062335 patent/WO2016193284A1/en not_active Ceased
- 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 BR BR112017025822A patent/BR112017025822B8/pt not_active IP Right Cessation
- 2016-06-01 CN CN201680032422.4A patent/CN107667090B/zh active Active
- 2016-06-01 EP EP16726113.0A patent/EP3303285B1/en active Active
- 2016-06-01 JP JP2017563077A patent/JP6807876B2/ja not_active Expired - Fee Related
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