JP2015512905A5 - - Google Patents
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- Publication number
- JP2015512905A5 JP2015512905A5 JP2015502278A JP2015502278A JP2015512905A5 JP 2015512905 A5 JP2015512905 A5 JP 2015512905A5 JP 2015502278 A JP2015502278 A JP 2015502278A JP 2015502278 A JP2015502278 A JP 2015502278A JP 2015512905 A5 JP2015512905 A5 JP 2015512905A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- group
- formula
- halogen
- compound
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 claims description 43
- 229910052736 halogen Inorganic materials 0.000 claims description 38
- 150000002367 halogens Chemical group 0.000 claims description 38
- 229910052739 hydrogen Inorganic materials 0.000 claims description 32
- 239000001257 hydrogen Substances 0.000 claims description 32
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 30
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 19
- 229910052717 sulfur Inorganic materials 0.000 claims description 19
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 18
- 241001465754 Metazoa Species 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 17
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 16
- 241000196324 Embryophyta Species 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 125000004414 alkyl thio group Chemical group 0.000 claims description 13
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 12
- -1 C 1 -C 6 - alkyl Chemical group 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 244000045947 parasite Species 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000000304 alkynyl group Chemical group 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
- 241000238631 Hexapoda Species 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 6
- 241000607479 Yersinia pestis Species 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 239000002689 soil Substances 0.000 claims description 6
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 4
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims description 4
- 241000239223 Arachnida Species 0.000 claims description 4
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims description 4
- 241000244206 Nematoda Species 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 125000002837 carbocyclic group Chemical group 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 208000015181 infectious disease Diseases 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 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 claims description 4
- 206010061217 Infestation Diseases 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 239000000575 pesticide Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 2
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 2
- 241000258937 Hemiptera Species 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 238000009395 breeding Methods 0.000 claims description 2
- 230000001488 breeding effect Effects 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001072 heteroaryl group Chemical group 0.000 claims description 2
- 230000009545 invasion Effects 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 230000000590 parasiticidal effect Effects 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 238000009331 sowing Methods 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 241000255777 Lepidoptera Species 0.000 claims 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
- 125000003341 7 membered heterocyclic group Chemical group 0.000 description 1
- 241000508744 Dichromothrips Species 0.000 description 1
- 241000233855 Orchidaceae Species 0.000 description 1
- 241001414989 Thysanoptera Species 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000004166 bioassay Methods 0.000 description 1
- 125000000232 haloalkynyl group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261617115P | 2012-03-29 | 2012-03-29 | |
| US61/617,115 | 2012-03-29 | ||
| PCT/EP2013/056285 WO2013144088A1 (en) | 2012-03-29 | 2013-03-25 | N-substituted hetero-bicyclic compounds and derivatives for combating animal pests ii |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015512905A JP2015512905A (ja) | 2015-04-30 |
| JP2015512905A5 true JP2015512905A5 (enExample) | 2017-06-01 |
Family
ID=47997497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015502278A Pending JP2015512905A (ja) | 2012-03-29 | 2013-03-25 | 有害動物を駆除するためのｎ−置換複素二環式化合物および誘導体ｉｉ |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9422280B2 (enExample) |
| EP (1) | EP2831076B1 (enExample) |
| JP (1) | JP2015512905A (enExample) |
| CN (1) | CN104220440B (enExample) |
| AR (1) | AR092313A1 (enExample) |
| ES (1) | ES2587954T3 (enExample) |
| MX (1) | MX2014011752A (enExample) |
| WO (1) | WO2013144088A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9334238B2 (en) | 2012-03-30 | 2016-05-10 | Basf Se | N-substituted pyridinylidenes for combating animal pests |
| US9963451B2 (en) | 2013-01-31 | 2018-05-08 | Mitsui Chemicals Agro, Inc. | Fused ring pyrimidine compound and pest control agent containing the same |
| EA201600270A1 (ru) | 2013-09-19 | 2016-08-31 | Басф Се | N-ацилимино гетероциклические соединения |
| WO2016039444A1 (ja) * | 2014-09-12 | 2016-03-17 | 日本農薬株式会社 | イミダゾピリダジン化合物又はその塩類及び該化合物を含有する農園芸用殺虫剤並びにその使用方法 |
| US11570992B2 (en) * | 2016-04-01 | 2023-02-07 | Basf Se | Bicyclic compounds |
| SG10201800971RA (en) * | 2018-02-05 | 2019-09-27 | Nec Asia Pacific Pte Ltd | Method and system for motor function rehabilitation and monitoring a patient’s recovery |
| WO2020011808A1 (en) | 2018-07-13 | 2020-01-16 | Syngenta Crop Protection Ag | Pesticidally-active bicyclic heteroaromatic compounds |
| WO2020025658A1 (en) | 2018-08-03 | 2020-02-06 | Syngenta Crop Protection Ag | Pesticidally-active bicyclic heteroaromatic compounds |
| EP3833663A1 (en) | 2018-08-07 | 2021-06-16 | Syngenta Crop Protection AG | Pesticidally-active bicyclic heteroaromatic compounds |
| WO2020030754A1 (en) | 2018-08-10 | 2020-02-13 | Syngenta Crop Protection Ag | Pesticidally-active mesoionic bicyclic heteroaromatic compounds |
| WO2020035565A1 (en) | 2018-08-17 | 2020-02-20 | Syngenta Crop Protection Ag | Pesticidally-active mesoionic bicyclic heteroaromatic compounds |
| WO2020120694A1 (en) | 2018-12-14 | 2020-06-18 | Syngenta Participations Ag | Pesticidally-active bicyclic heteroaromatic compounds |
| WO2021144354A1 (en) | 2020-01-15 | 2021-07-22 | Syngenta Crop Protection Ag | Pesticidally-active bicyclic heteroaromatic compounds |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH461489A (de) | 1965-03-26 | 1968-08-31 | Geigy Ag J R | Verfahren zur Herstellung von neuen Oxazolderivaten |
| JPH07121909B2 (ja) | 1986-09-10 | 1995-12-25 | 日本バイエルアグロケム株式会社 | 新規複素環式化合物及び殺虫剤 |
| DE3639877A1 (de) | 1986-11-21 | 1988-05-26 | Bayer Ag | Hetarylalkyl substituierte 5- und 6-ringheterocyclen |
| JPH0710865B2 (ja) | 1987-06-26 | 1995-02-08 | 日本バイエルアグロケム株式会社 | ニトロ置換ヘテロ環式化合物及び殺虫剤 |
| EP0639569A4 (en) | 1991-03-11 | 1995-09-20 | Nippon Soda Co | NEW HETEROCYCLIC COMPOUND. |
| US5585492A (en) * | 1994-10-11 | 1996-12-17 | G. D. Searle & Co. | LTA4 Hydrolase inhibitors |
| US6015817A (en) * | 1996-12-05 | 2000-01-18 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| DE19838138A1 (de) | 1997-08-25 | 1999-03-04 | Novartis Ag | Isoxazol-Derivate |
| NZ528961A (en) * | 2001-04-20 | 2005-04-29 | Bayer Cropscience Ag | Novel insecticidal azoles |
| DE102006015456A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Bicyclische Enamino(thio)carbonylverbindungen |
| DE102006015467A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| DE102006015470A1 (de) | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
| UY30267A1 (es) * | 2006-04-13 | 2007-11-30 | Astrazeneca Ab | Nuevos derivados de la tioxantina , composiciones farmacéuticas que los contienen, procedimientos de preparacion y aplicaciones |
| WO2007125984A1 (ja) | 2006-04-28 | 2007-11-08 | Nihon Nohyaku Co., Ltd. | イソキサゾリン誘導体及び有害生物防除剤並びにその使用方法 |
| US20090054468A1 (en) * | 2007-08-23 | 2009-02-26 | Astrazeneca Ab | New Use 938 |
| EP2107058A1 (de) | 2008-03-31 | 2009-10-07 | Bayer CropScience AG | Substituierte Enaminothiocarbonylverbindungen |
| WO2010005692A2 (en) | 2008-06-16 | 2010-01-14 | E. I. Du Pont De Nemours And Company | Insecticidal cyclic carbonyl amidines |
| EP2959775A1 (en) | 2010-08-31 | 2015-12-30 | Meiji Seika Pharma Co., Ltd. | Pest control agent |
| AR085872A1 (es) | 2011-04-08 | 2013-10-30 | Basf Se | Derivados heterobiciclicos n-sustituidos utiles para combatir parasitos en plantas y/o animales, composiciones que los contienen y metodos para combatir dichas plagas |
| WO2013144223A1 (en) | 2012-03-30 | 2013-10-03 | Basf Se | N-substituted pyrimidinylidene compounds and derivatives for combating animal pests |
| US9334238B2 (en) | 2012-03-30 | 2016-05-10 | Basf Se | N-substituted pyridinylidenes for combating animal pests |
| WO2013149903A1 (en) | 2012-04-03 | 2013-10-10 | Basf Se | N- substituted hetero - bicyclic furanone derivatives for combating animal |
-
2013
- 2013-03-25 EP EP13712246.1A patent/EP2831076B1/en not_active Not-in-force
- 2013-03-25 MX MX2014011752A patent/MX2014011752A/es unknown
- 2013-03-25 WO PCT/EP2013/056285 patent/WO2013144088A1/en not_active Ceased
- 2013-03-25 ES ES13712246.1T patent/ES2587954T3/es active Active
- 2013-03-25 US US14/387,600 patent/US9422280B2/en not_active Expired - Fee Related
- 2013-03-25 JP JP2015502278A patent/JP2015512905A/ja active Pending
- 2013-03-25 CN CN201380018078.XA patent/CN104220440B/zh not_active Expired - Fee Related
- 2013-03-27 AR ARP130101055A patent/AR092313A1/es unknown
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