JP2005531621A5 - - Google Patents
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- Publication number
- JP2005531621A5 JP2005531621A5 JP2004516728A JP2004516728A JP2005531621A5 JP 2005531621 A5 JP2005531621 A5 JP 2005531621A5 JP 2004516728 A JP2004516728 A JP 2004516728A JP 2004516728 A JP2004516728 A JP 2004516728A JP 2005531621 A5 JP2005531621 A5 JP 2005531621A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- formula
- alkoxy
- haloalkyl
- 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
- 150000001875 compounds Chemical class 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 150000003839 salts Chemical group 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 239000000575 pesticide Substances 0.000 claims description 2
- 241000607479 Yersinia pestis Species 0.000 claims 3
- 239000012872 agrochemical composition Substances 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 239000002671 adjuvant Substances 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 13
- 125000001424 substituent group Chemical group 0.000 description 10
- -1 C 1 -C 6 alkyl Chemical group 0.000 description 8
- 125000006765 (C2-C6) haloalkenyloxy group Chemical group 0.000 description 7
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 description 5
- 125000004737 (C1-C6) haloalkoxy 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
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 4
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 3
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 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 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH11232002 | 2002-06-28 | ||
| PCT/EP2003/006846 WO2004002943A1 (en) | 2002-06-28 | 2003-06-27 | 4-(3,3-dihalo-allyloxy)phenoxy alkyl derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005531621A JP2005531621A (ja) | 2005-10-20 |
| JP2005531621A5 true JP2005531621A5 (https=) | 2010-02-18 |
| JP4468805B2 JP4468805B2 (ja) | 2010-05-26 |
Family
ID=29783979
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004516728A Expired - Lifetime JP4468805B2 (ja) | 2002-06-28 | 2003-06-27 | ４−（３，３−ジハロ−アリルオキシ）フェノキシアルキル誘導体 |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US7192965B2 (https=) |
| EP (1) | EP1517881B1 (https=) |
| JP (1) | JP4468805B2 (https=) |
| CN (1) | CN1681771A (https=) |
| AT (1) | ATE469879T1 (https=) |
| AU (1) | AU2003246623A1 (https=) |
| BR (1) | BR0312287A (https=) |
| CO (1) | CO5631428A2 (https=) |
| DE (1) | DE60332835D1 (https=) |
| IL (1) | IL165221A0 (https=) |
| MX (1) | MXPA04012429A (https=) |
| TW (1) | TW200406370A (https=) |
| WO (1) | WO2004002943A1 (https=) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200406152A (en) * | 2002-08-30 | 2004-05-01 | Syngenta Participations Ag | 4-(3,3-Dihalo-allyloxy) phenol derivatives having pesticidal properties |
| TW200507752A (en) | 2003-06-23 | 2005-03-01 | Syngenta Participations Ag | Pesticidally active ketone and oxime derivatives |
| EP1659863A2 (en) | 2003-08-26 | 2006-05-31 | Syngenta Participations AG | Pesticidally active phenol derivatives |
| US20090209598A1 (en) * | 2005-11-14 | 2009-08-20 | Michael Puhl | Resorcine Derivatives and Their Use as Pesticides |
| TW201111358A (en) * | 2009-06-18 | 2011-04-01 | Intervet Int Bv | Anthelmintic agents and their use |
| CN103965048B (zh) * | 2014-05-06 | 2016-02-17 | 西北农林科技大学 | 反式肉桂酸酯类化合物及其合成方法和应用 |
| CA3026211A1 (en) | 2016-06-13 | 2017-12-21 | Glaxosmithkline Intellectual Property Development Limited | Substituted pyridines as inhibitors of dnmt1 |
| CN116023531B (zh) * | 2021-10-26 | 2025-09-09 | 中国石油化工股份有限公司 | 芳香族酰胺化合物及其制备方法和应用 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR9506309A (pt) * | 1994-08-04 | 1997-08-05 | Sumitomo Chemical Co | Compostos de dihalopropeno agentes inseticidas/acaricidas contendo os mesmos e intermediários para a sua produção |
| TW307746B (https=) * | 1994-10-14 | 1997-06-11 | Sumitomo Chemical Co | |
| AU3856795A (en) | 1994-11-14 | 1996-06-06 | Sumitomo Chemical Company, Limited | Dihalopropene compounds, use thereof, and intermediates for production thereof |
| CA2211361A1 (en) * | 1995-03-20 | 1996-09-26 | Unilever Plc | Liquid cleansing formulations |
| DE69610204T2 (de) * | 1995-04-18 | 2001-05-03 | Sumitomo Chemical Co., Ltd. | Dihalopropen-verbindungen, diese enthaltende insektizide und intermediate zu ihrer herstellung |
| AU1399297A (en) * | 1996-01-24 | 1997-08-20 | Sumitomo Chemical Company, Limited | Dihalopropene compounds, their use as insecticides/acaricides and intermediates for their production |
| US6140274A (en) * | 1996-01-30 | 2000-10-31 | Sumitomo Chemical Company, Limited | Dihalopropene compounds, their use as insecticides/acaricides and intermediates for their production |
| ATE182575T1 (de) * | 1996-01-31 | 1999-08-15 | Sumitomo Chemical Co | Fluorpropenverbindung, diese enthaltendes insektizid, und zwischenverbindung zu deren herstellung |
| EP0975586B1 (en) * | 1997-04-08 | 2004-12-01 | Sumitomo Chemical Company, Limited | Oxime compounds, their use, and intermediates for their production |
| TW200406152A (en) * | 2002-08-30 | 2004-05-01 | Syngenta Participations Ag | 4-(3,3-Dihalo-allyloxy) phenol derivatives having pesticidal properties |
| AR042344A1 (es) * | 2002-12-11 | 2005-06-15 | Syngenta Participations Ag | Derivados de 4-(3,3 - dihalo - aliloxi) fenol con propiedades pesticidas |
| JP2006511565A (ja) * | 2002-12-23 | 2006-04-06 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | 殺昆虫及び殺ダニ作用を有する２，６−ジハロ−４−（３，３−ジクロロ−アリルオキシ）−ベンジルアルコール誘導体 |
| TW200507752A (en) * | 2003-06-23 | 2005-03-01 | Syngenta Participations Ag | Pesticidally active ketone and oxime derivatives |
| EP1659863A2 (en) | 2003-08-26 | 2006-05-31 | Syngenta Participations AG | Pesticidally active phenol derivatives |
| US7723362B2 (en) | 2004-01-08 | 2010-05-25 | Syngenta Crop Protection, Inc. | Pesticidal heterocyclic dihaloallyl compounds |
-
2003
- 2003-06-26 TW TW092117378A patent/TW200406370A/zh unknown
- 2003-06-27 CN CNA038153041A patent/CN1681771A/zh active Pending
- 2003-06-27 BR BR0312287-5A patent/BR0312287A/pt not_active Application Discontinuation
- 2003-06-27 DE DE60332835T patent/DE60332835D1/de not_active Expired - Fee Related
- 2003-06-27 MX MXPA04012429A patent/MXPA04012429A/es unknown
- 2003-06-27 EP EP03761545A patent/EP1517881B1/en not_active Expired - Lifetime
- 2003-06-27 IL IL16522103A patent/IL165221A0/xx unknown
- 2003-06-27 AT AT03761545T patent/ATE469879T1/de not_active IP Right Cessation
- 2003-06-27 AU AU2003246623A patent/AU2003246623A1/en not_active Abandoned
- 2003-06-27 US US10/518,888 patent/US7192965B2/en not_active Expired - Fee Related
- 2003-06-27 JP JP2004516728A patent/JP4468805B2/ja not_active Expired - Lifetime
- 2003-06-27 WO PCT/EP2003/006846 patent/WO2004002943A1/en not_active Ceased
-
2004
- 2004-12-21 CO CO04127244A patent/CO5631428A2/es not_active Application Discontinuation
-
2007
- 2007-02-15 US US11/675,149 patent/US7414064B2/en not_active Expired - Fee Related
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