JP2016523228A5 - - Google Patents
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- Publication number
- JP2016523228A5 JP2016523228A5 JP2016517255A JP2016517255A JP2016523228A5 JP 2016523228 A5 JP2016523228 A5 JP 2016523228A5 JP 2016517255 A JP2016517255 A JP 2016517255A JP 2016517255 A JP2016517255 A JP 2016517255A JP 2016523228 A5 JP2016523228 A5 JP 2016523228A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- group
- alkoxy
- substituted
- cycloalkyl
- 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
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 65
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 35
- 125000001424 substituent group Chemical group 0.000 claims 35
- 150000001875 compounds Chemical class 0.000 claims 31
- 229910052736 halogen Inorganic materials 0.000 claims 31
- 150000002367 halogens Chemical class 0.000 claims 31
- -1 cyano, hydroxy Chemical group 0.000 claims 30
- 229910052717 sulfur Inorganic materials 0.000 claims 30
- 229910052760 oxygen Inorganic materials 0.000 claims 29
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 24
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 24
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 23
- 125000004432 carbon atom Chemical group C* 0.000 claims 22
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 19
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 17
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims 17
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 15
- 229910052757 nitrogen Inorganic materials 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 13
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 12
- 125000005842 heteroatom Chemical group 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 11
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 11
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 11
- 125000002947 alkylene group Chemical group 0.000 claims 11
- 229910052799 carbon Inorganic materials 0.000 claims 11
- 125000004093 cyano group Chemical group *C#N 0.000 claims 11
- 150000003254 radicals Chemical class 0.000 claims 11
- 150000003839 salts Chemical class 0.000 claims 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 10
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 10
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 10
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 10
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 9
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 9
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 9
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 8
- 125000001309 chloro group Chemical group Cl* 0.000 claims 7
- 125000004122 cyclic group Chemical group 0.000 claims 7
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 claims 6
- 125000004438 haloalkoxy group Chemical group 0.000 claims 6
- 150000002431 hydrogen Chemical class 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 5
- 239000000460 chlorine Substances 0.000 claims 5
- 125000004433 nitrogen atom Chemical class N* 0.000 claims 5
- 125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Substances 0.000 claims 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 4
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 125000002950 monocyclic group Chemical group 0.000 claims 4
- 125000004043 oxo group Chemical group O=* 0.000 claims 4
- 125000006413 ring segment Chemical group 0.000 claims 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 4
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 4
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 3
- 125000005862 (C1-C6)alkanoyl group Chemical group 0.000 claims 3
- 125000002015 acyclic group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 125000003367 polycyclic group Chemical group 0.000 claims 3
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 2
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 2
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims 2
- 125000006763 (C3-C9) cycloalkyl group Chemical group 0.000 claims 2
- YKYIFUROKBDHCY-ONEGZZNKSA-N (e)-4-ethoxy-1,1,1-trifluorobut-3-en-2-one Chemical group CCO\C=C\C(=O)C(F)(F)F YKYIFUROKBDHCY-ONEGZZNKSA-N 0.000 claims 2
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 claims 2
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 239000004009 herbicide Substances 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 2
- 239000005648 plant growth regulator Substances 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 1
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 230000000895 acaricidal effect Effects 0.000 claims 1
- 239000000642 acaricide Substances 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 239000003905 agrochemical Substances 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 244000038559 crop plants Species 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000003337 fertilizer Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 239000005645 nematicide Substances 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13171035 | 2013-06-07 | ||
| EP13171035.2 | 2013-06-07 | ||
| PCT/EP2014/061328 WO2014195253A1 (en) | 2013-06-07 | 2014-06-02 | Substituted 5-hydroxy-2,3-diphenylpentanonitrile derivatives, processes for their preparation and their use as herbicides and/or plant growth regulators |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016523228A JP2016523228A (ja) | 2016-08-08 |
| JP2016523228A5 true JP2016523228A5 (https=) | 2017-07-20 |
| JP6466923B2 JP6466923B2 (ja) | 2019-02-06 |
Family
ID=48570008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016517255A Expired - Fee Related JP6466923B2 (ja) | 2013-06-07 | 2014-06-02 | 置換された５−ヒドロキシ−２，３−ジフェニルペンタノニトリル誘導体、それの製造方法、ならびにそれの除草剤および／または植物成長調節剤としての使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10021877B2 (https=) |
| EP (1) | EP3003036B1 (https=) |
| JP (1) | JP6466923B2 (https=) |
| CN (1) | CN105451553A (https=) |
| AR (1) | AR096517A1 (https=) |
| BR (1) | BR112015030196A2 (https=) |
| WO (1) | WO2014195253A1 (https=) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3203841B1 (de) | 2014-10-08 | 2018-06-13 | Bayer CropScience Aktiengesellschaft | Substituierte 5-hydroxy-2-phenyl-3-heteroarylpentanonitrilderivate, verfahren zu deren herstellung und deren verwendung als herbizide und/oder pflanzenwachstumsregulatoren |
| CN110672753B (zh) * | 2019-11-04 | 2022-05-20 | 青海省农林科学院 | 一种氟咯草酮异构体的拆分和检测方法 |
| CN111990400B (zh) * | 2020-07-29 | 2021-07-23 | 浙江工业大学 | 一种二芳基戊烷类化合物在除草剂中的应用 |
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| MA19709A1 (fr) | 1982-02-17 | 1983-10-01 | Ciba Geigy Ag | Application de derives de quinoleine a la protection des plantes cultivees . |
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| JPS6087254A (ja) | 1983-10-19 | 1985-05-16 | Japan Carlit Co Ltd:The | 新規尿素化合物及びそれを含有する除草剤 |
| FR2561918A1 (fr) * | 1984-03-30 | 1985-10-04 | Hoechst Lab | Nouveaux medicaments appartenant a la famille des tetrahydropyrones-2 a action psychostimulante et leur procede de preparation |
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| WO2007023719A1 (ja) | 2005-08-22 | 2007-03-01 | Kumiai Chemical Industry Co., Ltd. | 薬害軽減剤及び薬害が軽減された除草剤組成物 |
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| WO2011003775A2 (de) | 2009-07-09 | 2011-01-13 | Basf Se | Substituierte cyanobutyrate mit herbizider wirkung |
| WO2011003776A2 (de) | 2009-07-09 | 2011-01-13 | Basf Se | Substituierte cyanobutyrate mit herbizider wirkung |
| US20120121508A1 (en) | 2009-07-27 | 2012-05-17 | Merck Sharp & Dohme Corp. | Radiolabeled cgrp antagonists |
| WO2011042378A1 (de) | 2009-10-09 | 2011-04-14 | Basf Se | Substituierte cyanobutyrate mit herbizider wirkung |
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| WO2012076513A1 (en) | 2010-12-09 | 2012-06-14 | F. Hoffmann-La Roche Ag | 3-cyano-1-hydroxymethyl-2-phenylpyrrolidine derivatives as inhibitors of mdm2-p53 interactions useful for the treatment of cancer |
| EP2693878B8 (de) | 2011-03-18 | 2018-08-29 | Bayer CropScience Aktiengesellschaft | Substituierte (3r,4r)-4-cyan-3,4-diphenylbutanoate, verfahren zu deren herstellung und deren verwendung als herbizide und pflanzenwachstumsregulatoren |
| US20140087945A1 (en) | 2011-03-18 | 2014-03-27 | Bayer Intellectual Property Gmbh | Substituted 4-cyan-3-(2,6-difluorophenyl)-4-phenylbutanoates, method for the production thereof and use thereof as herbicides and plant growth regulators |
| EP2731933B1 (de) * | 2011-07-15 | 2015-09-30 | Bayer Intellectual Property GmbH | 2,3-diphenyl-valeronitrilderivate, verfahren zu deren herstellung und deren verwendung als herbizide und pflanzenwachstumsregulatoren |
-
2014
- 2014-05-30 AR ARP140102149A patent/AR096517A1/es unknown
- 2014-06-02 EP EP14727513.5A patent/EP3003036B1/en not_active Not-in-force
- 2014-06-02 US US14/895,343 patent/US10021877B2/en not_active Expired - Fee Related
- 2014-06-02 CN CN201480043764.7A patent/CN105451553A/zh active Pending
- 2014-06-02 WO PCT/EP2014/061328 patent/WO2014195253A1/en not_active Ceased
- 2014-06-02 BR BR112015030196A patent/BR112015030196A2/pt not_active Application Discontinuation
- 2014-06-02 JP JP2016517255A patent/JP6466923B2/ja not_active Expired - Fee Related
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