JP2016529214A5 - - Google Patents
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- Publication number
- JP2016529214A5 JP2016529214A5 JP2016522421A JP2016522421A JP2016529214A5 JP 2016529214 A5 JP2016529214 A5 JP 2016529214A5 JP 2016522421 A JP2016522421 A JP 2016522421A JP 2016522421 A JP2016522421 A JP 2016522421A JP 2016529214 A5 JP2016529214 A5 JP 2016529214A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- group
- substituents
- groups
- 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
- 125000001424 substituent group Chemical group 0.000 claims 38
- 125000005842 heteroatom Chemical group 0.000 claims 30
- 125000000623 heterocyclic group Chemical group 0.000 claims 26
- 229910052739 hydrogen Inorganic materials 0.000 claims 25
- 239000001257 hydrogen Substances 0.000 claims 25
- 150000002431 hydrogen Chemical class 0.000 claims 22
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 21
- 229910052760 oxygen Inorganic materials 0.000 claims 20
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 19
- 150000001875 compounds Chemical class 0.000 claims 19
- 229910052717 sulfur Inorganic materials 0.000 claims 19
- 125000001931 aliphatic group Chemical group 0.000 claims 18
- 229910052736 halogen Inorganic materials 0.000 claims 18
- 150000002367 halogens Chemical class 0.000 claims 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 18
- 229920006395 saturated elastomer Polymers 0.000 claims 17
- -1 C 1 -C 6 -Alkoxy Chemical group 0.000 claims 15
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 14
- 229910052799 carbon Inorganic materials 0.000 claims 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims 13
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 12
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 11
- 241000607479 Yersinia pestis Species 0.000 claims 9
- 125000002723 alicyclic group Chemical group 0.000 claims 9
- 125000004438 haloalkoxy group Chemical group 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 8
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 7
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 7
- 125000004432 carbon atom Chemical group C* 0.000 claims 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 7
- 229910052757 nitrogen Inorganic materials 0.000 claims 7
- KWEDUNSJJZVRKR-UHFFFAOYSA-N carbononitridic azide Chemical compound [N-]=[N+]=NC#N KWEDUNSJJZVRKR-UHFFFAOYSA-N 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 5
- 241001465754 Metazoa Species 0.000 claims 5
- 125000000304 alkynyl group Chemical group 0.000 claims 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 5
- 239000000463 material Substances 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 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 4
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 4
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 3
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 3
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 230000009545 invasion Effects 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 2
- 125000002837 carbocyclic group Chemical group 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- 125000000232 haloalkynyl group Chemical group 0.000 claims 2
- 208000015181 infectious disease Diseases 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 2
- 125000006413 ring segment Chemical group 0.000 claims 2
- 239000002689 soil Substances 0.000 claims 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- GUUULVAMQJLDSY-UHFFFAOYSA-N 4,5-dihydro-1,2-thiazole Chemical class C1CC=NS1 GUUULVAMQJLDSY-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 238000009395 breeding Methods 0.000 claims 1
- 230000001488 breeding effect Effects 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 150000002466 imines Chemical class 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361838365P | 2013-06-24 | 2013-06-24 | |
| US61/838,365 | 2013-06-24 | ||
| US201461940506P | 2014-02-17 | 2014-02-17 | |
| US61/940,506 | 2014-02-17 | ||
| PCT/EP2014/063102 WO2014206908A1 (en) | 2013-06-24 | 2014-06-23 | Isothiazoline compounds substituted with a carbobicyclic group |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016529214A JP2016529214A (ja) | 2016-09-23 |
| JP2016529214A5 true JP2016529214A5 (enExample) | 2017-07-06 |
| JP6484233B2 JP6484233B2 (ja) | 2019-03-13 |
Family
ID=51033173
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016522421A Expired - Fee Related JP6484233B2 (ja) | 2013-06-24 | 2014-06-23 | 炭素二環式基により置換されているイソチアゾリン化合物 |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP3013808B1 (enExample) |
| JP (1) | JP6484233B2 (enExample) |
| CN (1) | CN105473563A (enExample) |
| BR (1) | BR112015032327A2 (enExample) |
| CA (1) | CA2916829A1 (enExample) |
| ES (1) | ES2818925T3 (enExample) |
| MX (1) | MX374349B (enExample) |
| WO (1) | WO2014206908A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3102563B1 (en) | 2014-02-03 | 2019-04-10 | Basf Se | Cyclopentene and cyclopentadiene compounds for controlling invertebrate pests |
| CN108314630B (zh) * | 2018-02-08 | 2020-11-06 | 广西民族大学 | 一种肟醚类衍生物及其制备方法与应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009286773A (ja) * | 2008-03-14 | 2009-12-10 | Bayer Cropscience Ag | 殺虫性縮環式アリール類 |
| EP2755969B1 (en) * | 2011-09-13 | 2017-01-18 | Syngenta Participations AG | Isothiazoline derivatives as insecticidal compounds |
| WO2014001121A1 (en) * | 2012-06-25 | 2014-01-03 | Syngenta Participations Ag | Isothiazole derivatives as insecticidal compounds |
-
2014
- 2014-06-23 JP JP2016522421A patent/JP6484233B2/ja not_active Expired - Fee Related
- 2014-06-23 WO PCT/EP2014/063102 patent/WO2014206908A1/en not_active Ceased
- 2014-06-23 ES ES14734070T patent/ES2818925T3/es active Active
- 2014-06-23 MX MX2015018014A patent/MX374349B/es active IP Right Grant
- 2014-06-23 CA CA2916829A patent/CA2916829A1/en not_active Abandoned
- 2014-06-23 EP EP14734070.7A patent/EP3013808B1/en active Active
- 2014-06-23 CN CN201480043334.5A patent/CN105473563A/zh active Pending
- 2014-06-23 BR BR112015032327A patent/BR112015032327A2/pt not_active Application Discontinuation
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