JP2016534037A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016534037A5 JP2016534037A5 JP2016520645A JP2016520645A JP2016534037A5 JP 2016534037 A5 JP2016534037 A5 JP 2016534037A5 JP 2016520645 A JP2016520645 A JP 2016520645A JP 2016520645 A JP2016520645 A JP 2016520645A JP 2016534037 A5 JP2016534037 A5 JP 2016534037A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- haloalkyl
- halogen
- group
- 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
- 229910052736 halogen Inorganic materials 0.000 claims description 71
- 150000002367 halogens Chemical class 0.000 claims description 71
- 125000000217 alkyl group Chemical group 0.000 claims description 60
- 150000001875 compounds Chemical class 0.000 claims description 45
- 229910052739 hydrogen Inorganic materials 0.000 claims description 45
- 239000001257 hydrogen Substances 0.000 claims description 45
- 150000002431 hydrogen Chemical group 0.000 claims description 36
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 31
- 229910052760 oxygen Inorganic materials 0.000 claims description 31
- 125000003545 alkoxy group Chemical group 0.000 claims description 30
- 229910052717 sulfur Inorganic materials 0.000 claims description 27
- -1 C 1 -C 4 alkyl Chemical group 0.000 claims description 26
- 125000005842 heteroatom Chemical group 0.000 claims description 24
- 125000001188 haloalkyl group Chemical group 0.000 claims description 21
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 21
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 19
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
- 229920006395 saturated elastomer Polymers 0.000 claims description 16
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 15
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 13
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 13
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 125000004429 atom Chemical group 0.000 claims description 9
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 9
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 8
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 8
- 125000002619 bicyclic group Chemical group 0.000 claims description 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 230000002363 herbicidal effect Effects 0.000 claims description 7
- 125000001072 heteroaryl group Chemical group 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000002950 monocyclic group Chemical group 0.000 claims description 7
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 5
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims description 4
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 4
- 241000196324 Embryophyta Species 0.000 claims description 4
- 150000001204 N-oxides Chemical class 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 239000004009 herbicide Substances 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 150000003839 salts Chemical group 0.000 claims description 4
- 244000045561 useful plants Species 0.000 claims description 4
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 3
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 3
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 3
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims description 3
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 3
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 3
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 3
- 125000000304 alkynyl group Chemical group 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 125000004104 aryloxy group Chemical group 0.000 claims description 3
- 239000002671 adjuvant Substances 0.000 claims description 2
- 125000005200 aryloxy carbonyloxy group Chemical group 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 125000000262 haloalkenyl group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000004966 cyanoalkyl group Chemical group 0.000 description 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 4
- 125000006002 1,1-difluoroethyl group Chemical group 0.000 description 2
- 125000003302 alkenyloxy group Chemical group 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000002757 morpholinyl group Chemical group 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- IGERFAHWSHDDHX-UHFFFAOYSA-N 1,3-dioxanyl Chemical group [CH]1OCCCO1 IGERFAHWSHDDHX-UHFFFAOYSA-N 0.000 description 1
- JPRPJUMQRZTTED-UHFFFAOYSA-N 1,3-dioxolanyl Chemical group [CH]1OCCO1 JPRPJUMQRZTTED-UHFFFAOYSA-N 0.000 description 1
- 125000004776 1-fluoroethyl group Chemical group [H]C([H])([H])C([H])(F)* 0.000 description 1
- 0 CC(C)(C)OC(N*I)=N Chemical compound CC(C)(C)OC(N*I)=N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 description 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000005133 alkynyloxy group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 125000002636 imidazolinyl group Chemical group 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 230000000116 mitigating effect Effects 0.000 description 1
- 125000006574 non-aromatic ring group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000004621 quinuclidinyl group Chemical group N12C(CC(CC1)CC2)* 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN2977/DEL/2013 | 2013-10-07 | ||
| IN2977DE2013 IN2013DE02977A (OSRAM) | 2013-10-07 | 2014-10-02 | |
| PCT/EP2014/071167 WO2015052076A1 (en) | 2013-10-07 | 2014-10-02 | Herbicidal compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016534037A JP2016534037A (ja) | 2016-11-04 |
| JP2016534037A5 true JP2016534037A5 (OSRAM) | 2017-11-09 |
| JP6419171B2 JP6419171B2 (ja) | 2018-11-07 |
Family
ID=51659651
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016520645A Active JP6419171B2 (ja) | 2013-10-07 | 2014-10-02 | 除草性化合物 |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US20160264547A1 (OSRAM) |
| EP (1) | EP3054773B1 (OSRAM) |
| JP (1) | JP6419171B2 (OSRAM) |
| KR (1) | KR20160067950A (OSRAM) |
| CN (2) | CN111961033A (OSRAM) |
| AR (1) | AR097936A1 (OSRAM) |
| AU (1) | AU2014333967B2 (OSRAM) |
| BR (1) | BR112016007356B1 (OSRAM) |
| CA (1) | CA2924243C (OSRAM) |
| EA (1) | EA032393B1 (OSRAM) |
| ES (1) | ES2910437T3 (OSRAM) |
| HK (1) | HK1222980A1 (OSRAM) |
| IN (1) | IN2013DE02977A (OSRAM) |
| UA (1) | UA118035C2 (OSRAM) |
| UY (1) | UY35769A (OSRAM) |
| WO (1) | WO2015052076A1 (OSRAM) |
| ZA (1) | ZA201601788B (OSRAM) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201505852D0 (en) * | 2015-04-07 | 2015-05-20 | Syngenta Participations Ag | Herbicidal mixtures |
| GB201604970D0 (en) * | 2016-03-23 | 2016-05-04 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| GB201604969D0 (en) * | 2016-03-23 | 2016-05-04 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| ES2899104T3 (es) * | 2016-03-23 | 2022-03-10 | Syngenta Participations Ag | Herbicidas |
| CA3019878A1 (en) * | 2016-04-29 | 2017-11-02 | Syngenta Participations Ag | Process for the preparation of herbicidal compounds |
| AR108107A1 (es) * | 2016-04-29 | 2018-07-18 | Syngenta Participations Ag | Proceso para preparar compuestos herbicidas |
| US11547706B2 (en) | 2016-06-08 | 2023-01-10 | President And Fellows Of Harvard College | Methods and compositions for reducing tactile dysfunction and anxiety associated with autism spectrum disorder, Rett syndrome, and Fragile X syndrome |
| GB201612748D0 (en) | 2016-07-22 | 2016-09-07 | Syngenta Participations Ag | Method of controlling plants |
| JP2019526547A (ja) | 2016-08-11 | 2019-09-19 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 置換されているピラゾリニル誘導体、それらを製造する方法、並びに、除草剤及び／又は植物成長調節剤としてのそれらの使用 |
| GB201617050D0 (en) * | 2016-10-07 | 2016-11-23 | Syngenta Participations Ag | Herbicidal mixtures |
| GB201617062D0 (en) * | 2016-10-07 | 2016-11-23 | Syngenta Participations Ag | Herbicidal mixtures |
| WO2019006358A1 (en) * | 2017-06-30 | 2019-01-03 | Syngenta Participations Ag | HERBICIDE COMPOSITION AND METHOD OF USE |
| GB201715324D0 (en) * | 2017-09-22 | 2017-11-08 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| EP3797097A4 (en) | 2018-05-22 | 2022-03-09 | President and Fellows of Harvard College | Compositions and methods for reducing tactile dysfunction, anxiety, and social impairment |
| US11434244B2 (en) | 2018-05-29 | 2022-09-06 | President And Fellows Of Harvard College | Compositions and methods for reducing tactile dysfunction, anxiety, and social impairment |
| GB201818117D0 (en) | 2018-11-06 | 2018-12-19 | Syngenta Participations Ag | Enantioselective process |
| GB201901559D0 (en) * | 2019-02-05 | 2019-03-27 | Syngenta Crop Protection Ag | Herbicidal compositions |
| WO2020164925A1 (en) | 2019-02-15 | 2020-08-20 | Syngenta Crop Protection Ag | Herbicidal compositions |
| WO2020198275A1 (en) | 2019-03-25 | 2020-10-01 | President And Fellows Of Harvard College | Compositions and methods for reducing tactile dysfunction, anxiety, and social impairment |
| CN113045548B (zh) * | 2020-07-15 | 2022-01-28 | 周银平 | 一种化合物、除草组合物及其用途 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2194369B1 (OSRAM) * | 1972-08-04 | 1980-04-25 | Roussel Uclaf | |
| CA1031349A (en) * | 1973-12-26 | 1978-05-16 | John Krenzer | Thiadiazolylimidazolidinones |
| US4130714A (en) * | 1977-05-23 | 1978-12-19 | Pfizer Inc. | Hydantoin therapeutic agents |
| US4426527A (en) * | 1982-02-12 | 1984-01-17 | Ppg Industries, Inc. | 3-[5- Or 3-substituted-1,2,4-oxadiazol-3- or -5-yl]-1-substituted-4-substituted-5-substituted or unsubstituted-2-imidazolidinones |
| JPS608290A (ja) * | 1983-06-27 | 1985-01-17 | ピーピージー・インダストリィズ・インコーポレイテッド | ３−〔５−もしくは３−置換−１・２・４−オキサジアゾル−３−もしくは−５−イル〕−１−置換−４−置換−５−置換もしくは非置換−２−イミダゾリジノン |
| ATE37182T1 (de) * | 1983-08-02 | 1988-09-15 | American Cyanamid Co | Imidazolinone und imidazolidinthione, verfahren zu deren herstellung und verwendung dieser verbindungen als herbizide. |
| AU568759B2 (en) * | 1984-07-17 | 1988-01-07 | Eli Lilly And Company | Pyridazinylimidazolinones |
| US4604127A (en) * | 1984-07-17 | 1986-08-05 | Eli Lilly And Company | Herbicidal pyridazinylimidazolidinone compounds |
| US4600430A (en) * | 1985-02-22 | 1986-07-15 | Eli Lilly And Company | Pyridinylimidazolidinone compounds |
| DE3604042A1 (de) * | 1986-02-08 | 1987-08-13 | Hoechst Ag | Imidazolidin(thi)on-derivate, verfahren zu ihrer herstellung sowie ihre verwendung im pflanzenschutz |
| FI90869C (fi) * | 1986-11-14 | 1994-04-11 | Tanabe Seiyaku Co | Menetelmä lääkeaineena käyttökelpoisten imidatsolidinonijohdannaisten valmistamiseksi |
| CN1175255A (zh) * | 1994-12-27 | 1998-03-04 | 财团法人相模中央化学研究院 | 乙内酰脲衍生物、它们的制备方法和含有这些衍生物作为活性组分的除草剂 |
| AU2006327217A1 (en) * | 2005-11-28 | 2007-06-28 | Mallinckrodt Inc. | Improved method of preparation for Imidazolepyridines |
-
2014
- 2014-02-10 UA UAA201604929A patent/UA118035C2/uk unknown
- 2014-10-02 CN CN202010834225.2A patent/CN111961033A/zh active Pending
- 2014-10-02 EA EA201600317A patent/EA032393B1/ru not_active IP Right Cessation
- 2014-10-02 WO PCT/EP2014/071167 patent/WO2015052076A1/en not_active Ceased
- 2014-10-02 US US15/027,768 patent/US20160264547A1/en not_active Abandoned
- 2014-10-02 KR KR1020167012003A patent/KR20160067950A/ko not_active Ceased
- 2014-10-02 JP JP2016520645A patent/JP6419171B2/ja active Active
- 2014-10-02 AU AU2014333967A patent/AU2014333967B2/en active Active
- 2014-10-02 HK HK16111452.0A patent/HK1222980A1/zh unknown
- 2014-10-02 CA CA2924243A patent/CA2924243C/en active Active
- 2014-10-02 EP EP14780489.2A patent/EP3054773B1/en active Active
- 2014-10-02 ES ES14780489T patent/ES2910437T3/es active Active
- 2014-10-02 IN IN2977DE2013 patent/IN2013DE02977A/en unknown
- 2014-10-02 CN CN201480055222.1A patent/CN105636439A/zh active Pending
- 2014-10-02 BR BR112016007356-8A patent/BR112016007356B1/pt active IP Right Grant
- 2014-10-03 UY UY0001035769A patent/UY35769A/es not_active Application Discontinuation
- 2014-10-06 AR ARP140103717A patent/AR097936A1/es active IP Right Grant
-
2016
- 2016-03-15 ZA ZA2016/01788A patent/ZA201601788B/en unknown
-
2018
- 2018-12-17 US US16/222,900 patent/US11608323B2/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2016534037A5 (OSRAM) | ||
| JP2012140432A5 (OSRAM) | ||
| MX2023006047A (es) | Degradadores selectivos del receptor de estrogeno. | |
| HRP20220899T1 (hr) | Spojevi policikličkog karbamoilpiridona i njihova farmaceutska uporaba | |
| JP2016536364A5 (OSRAM) | ||
| JP2016536363A5 (OSRAM) | ||
| RU2014140739A (ru) | Соединения на основе имидазо[1, 2-b]пиридазина, композиции таких соединений и способы их применения | |
| EP4248988A3 (en) | Alkenyl substituted 2,5-piperazinediones and their use in compositions for delivering an agent to a subject or cell | |
| MX384752B (es) | ANTAGONISTAS SOLUBLES DE RECEPTOR DE C5a (C5aR). | |
| EP4252848A3 (en) | Oxysterols and methods of use thereof | |
| JP2014525420A5 (OSRAM) | ||
| EA201692095A1 (ru) | Имидазо[4,5-c]хинолин-2-оновые соединения и их применение в лечении рака | |
| MY189118A (en) | Pyrazolo[1,5-a]pyrazin-4-yl derivatives | |
| JP2017509586A5 (OSRAM) | ||
| JP2016525135A5 (OSRAM) | ||
| JP2016525136A5 (OSRAM) | ||
| MX2019015371A (es) | Derivados de dihidro-pirrolo-piridina. | |
| JP2010539110A5 (OSRAM) | ||
| JP2019512535A5 (OSRAM) | ||
| JP2019504050A5 (OSRAM) | ||
| BR112012013511A2 (pt) | derivados de difenil-pirazolopiridinas, sua preparação e seu uso como não moduladores do receptor nuclear | |
| AU2018253590A1 (en) | Imidazopyridazine compounds | |
| AR102213A1 (es) | Inhibidores de la biosíntesis de sulfato de heparano para el tratamiento de enfermedades | |
| JP2012513416A5 (OSRAM) | ||
| JP2019514849A5 (OSRAM) |