JP2005516038A5 - - Google Patents
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- JP2005516038A5 JP2005516038A5 JP2003562104A JP2003562104A JP2005516038A5 JP 2005516038 A5 JP2005516038 A5 JP 2005516038A5 JP 2003562104 A JP2003562104 A JP 2003562104A JP 2003562104 A JP2003562104 A JP 2003562104A JP 2005516038 A5 JP2005516038 A5 JP 2005516038A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl ring
- group
- halogen
- chloro
- alkyl
- 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.)
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 45
- 229910052736 halogen Inorganic materials 0.000 claims description 38
- 150000002367 halogens Chemical class 0.000 claims description 37
- 125000001424 substituent group Chemical group 0.000 claims description 21
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 9
- 229910052740 iodine Inorganic materials 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 150000001204 N-oxides Chemical class 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 29
- -1 C 1 -C 4 alkoxy Chemical group 0.000 description 17
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 12
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 11
- 229910052799 carbon Inorganic materials 0.000 description 11
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 10
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 description 9
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 description 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 3
- 241000607479 Yersinia pestis Species 0.000 description 3
- 125000004663 dialkyl amino group Chemical group 0.000 description 3
- 125000000262 haloalkenyl group Chemical group 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000995027 Empoasca fabae Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 description 1
- AALVFNLYRMIBLF-UHFFFAOYSA-N 1-[5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-6,8-dichloro-3-methyl-2h-quinazolin-4-one Chemical compound C12=C(Cl)C=C(Cl)C=C2C(=O)N(C)CN1C(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl AALVFNLYRMIBLF-UHFFFAOYSA-N 0.000 description 1
- QHCXISNFHMEFAW-UHFFFAOYSA-N 1-[5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-6,8-dichloro-3-propan-2-yl-2h-quinazolin-4-one Chemical compound C12=C(Cl)C=C(Cl)C=C2C(=O)N(C(C)C)CN1C(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl QHCXISNFHMEFAW-UHFFFAOYSA-N 0.000 description 1
- FHRJKCAOBDJIIY-UHFFFAOYSA-N 1-[5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-6-chloro-3,8-dimethyl-2h-quinazolin-4-one Chemical compound C12=C(C)C=C(Cl)C=C2C(=O)N(C)CN1C(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl FHRJKCAOBDJIIY-UHFFFAOYSA-N 0.000 description 1
- WHXJBPOMUIMDOV-UHFFFAOYSA-N 1-[5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-6-chloro-8-methyl-3-propan-2-yl-2h-quinazolin-4-one Chemical compound C12=C(C)C=C(Cl)C=C2C(=O)N(C(C)C)CN1C(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl WHXJBPOMUIMDOV-UHFFFAOYSA-N 0.000 description 1
- QGIUWOGFAKDUAF-UHFFFAOYSA-N 1-[5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-8-methyl-3-propan-2-yl-2h-quinazolin-4-one Chemical compound C12=C(C)C=CC=C2C(=O)N(C(C)C)CN1C(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl QGIUWOGFAKDUAF-UHFFFAOYSA-N 0.000 description 1
- GFJOUIQLXCWIII-UHFFFAOYSA-N 6,8-dichloro-1-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazole-3-carbonyl]-2,3-dihydroquinazolin-4-one Chemical compound N1=C(C(F)(F)F)C=C(C(=O)N2C3=C(Cl)C=C(Cl)C=C3C(=O)NC2)N1C1=NC=CC=C1Cl GFJOUIQLXCWIII-UHFFFAOYSA-N 0.000 description 1
- VVSUTQZXADBCHF-UHFFFAOYSA-N 6,8-dichloro-1-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazole-3-carbonyl]-3-methyl-2h-quinazolin-4-one Chemical compound C12=C(Cl)C=C(Cl)C=C2C(=O)N(C)CN1C(=O)C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl VVSUTQZXADBCHF-UHFFFAOYSA-N 0.000 description 1
- UEISRGHJWJEKTH-UHFFFAOYSA-N 6,8-dichloro-1-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazole-3-carbonyl]-3-propan-2-yl-2h-quinazolin-4-one Chemical compound C12=C(Cl)C=C(Cl)C=C2C(=O)N(C(C)C)CN1C(=O)C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl UEISRGHJWJEKTH-UHFFFAOYSA-N 0.000 description 1
- FSTJCJUBVFTDMM-UHFFFAOYSA-N 6,8-dichloro-1-[5-chloro-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-3-methyl-2h-quinazolin-4-one Chemical compound C12=C(Cl)C=C(Cl)C=C2C(=O)N(C)CN1C(=O)C1=CC(Cl)=NN1C1=NC=CC=C1Cl FSTJCJUBVFTDMM-UHFFFAOYSA-N 0.000 description 1
- BHRRQKKYRCUMTF-UHFFFAOYSA-N 6,8-dichloro-1-[5-chloro-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-3-propan-2-yl-2h-quinazolin-4-one Chemical compound C12=C(Cl)C=C(Cl)C=C2C(=O)N(C(C)C)CN1C(=O)C1=CC(Cl)=NN1C1=NC=CC=C1Cl BHRRQKKYRCUMTF-UHFFFAOYSA-N 0.000 description 1
- KOJCBLUZIAINAO-UHFFFAOYSA-N 6-bromo-1-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazole-3-carbonyl]-3,8-dimethylquinazoline-2,4-dione Chemical compound CC1=CC(Br)=CC(C(N(C)C2=O)=O)=C1N2C(=O)C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl KOJCBLUZIAINAO-UHFFFAOYSA-N 0.000 description 1
- MKHMZLZFYMPDIJ-UHFFFAOYSA-N 6-bromo-1-[5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-3,8-dimethylquinazoline-2,4-dione Chemical compound CC1=CC(Br)=CC(C(N(C)C2=O)=O)=C1N2C(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl MKHMZLZFYMPDIJ-UHFFFAOYSA-N 0.000 description 1
- WSOMGQXDTYFMEO-UHFFFAOYSA-N 6-bromo-1-[5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-8-methyl-3-propan-2-ylquinazoline-2,4-dione Chemical compound C12=C(C)C=C(Br)C=C2C(=O)N(C(C)C)C(=O)N1C(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl WSOMGQXDTYFMEO-UHFFFAOYSA-N 0.000 description 1
- SJVAZPXRKGKGIN-UHFFFAOYSA-N 6-chloro-1-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazole-3-carbonyl]-3,8-dimethyl-2h-quinazolin-4-one Chemical compound C12=C(C)C=C(Cl)C=C2C(=O)N(C)CN1C(=O)C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl SJVAZPXRKGKGIN-UHFFFAOYSA-N 0.000 description 1
- LRNIRWRPYJXUGJ-UHFFFAOYSA-N 6-chloro-1-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazole-3-carbonyl]-8-methyl-3-propan-2-yl-2h-quinazolin-4-one Chemical compound C12=C(C)C=C(Cl)C=C2C(=O)N(C(C)C)CN1C(=O)C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl LRNIRWRPYJXUGJ-UHFFFAOYSA-N 0.000 description 1
- VSQCHSNHIWPDQI-UHFFFAOYSA-N 6-chloro-1-[5-chloro-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-3,8-dimethyl-2h-quinazolin-4-one Chemical compound C12=C(C)C=C(Cl)C=C2C(=O)N(C)CN1C(=O)C1=CC(Cl)=NN1C1=NC=CC=C1Cl VSQCHSNHIWPDQI-UHFFFAOYSA-N 0.000 description 1
- PDBNHPOQFNFYQV-UHFFFAOYSA-N 6-chloro-1-[5-chloro-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]-8-methyl-3-propan-2-yl-2h-quinazolin-4-one Chemical compound C12=C(C)C=C(Cl)C=C2C(=O)N(C(C)C)CN1C(=O)C1=CC(Cl)=NN1C1=NC=CC=C1Cl PDBNHPOQFNFYQV-UHFFFAOYSA-N 0.000 description 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 description 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 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 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35063202P | 2002-01-22 | 2002-01-22 | |
| PCT/US2003/001482 WO2003062226A1 (en) | 2002-01-22 | 2003-01-16 | Quinazoline(di) ones for invertebrate pest control |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005516038A JP2005516038A (ja) | 2005-06-02 |
| JP2005516038A5 true JP2005516038A5 (https=) | 2006-11-02 |
| JP4394953B2 JP4394953B2 (ja) | 2010-01-06 |
Family
ID=27613409
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003562104A Expired - Lifetime JP4394953B2 (ja) | 2002-01-22 | 2003-01-16 | 無脊椎有害生物防除のためのキナゾリン（ジ）オン |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US7241767B2 (https=) |
| EP (1) | EP1467988B1 (https=) |
| JP (1) | JP4394953B2 (https=) |
| KR (1) | KR101011837B1 (https=) |
| CN (2) | CN100349890C (https=) |
| AU (2) | AU2003212811B2 (https=) |
| BR (1) | BR0307178A (https=) |
| ES (1) | ES2427141T3 (https=) |
| MX (2) | MX258385B (https=) |
| RU (1) | RU2315765C2 (https=) |
| WO (1) | WO2003062226A1 (https=) |
| ZA (1) | ZA200404022B (https=) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI312274B (en) * | 2001-08-13 | 2009-07-21 | Du Pont | Method for controlling particular insect pests by applying anthranilamide compounds |
| AR036872A1 (es) | 2001-08-13 | 2004-10-13 | Du Pont | Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados |
| AU2002331706B2 (en) * | 2001-08-15 | 2009-01-22 | E.I. Du Pont De Nemours And Company | Ortho-substituted aryl amides for controlling invertebrate pests |
| BR0212183B1 (pt) * | 2001-08-16 | 2014-10-21 | Du Pont | composto de antranilamida substituída, seus n-óxidos e sais, método para o controle de uma praga invertebrada e composição para o controle de uma praga invertebrada |
| TWI283164B (en) * | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
| US20040110777A1 (en) * | 2001-12-03 | 2004-06-10 | Annis Gary David | Quinazolinones and pyridinylpyrimidinones for controlling invertebrate pests |
| BR0307178A (pt) | 2002-01-22 | 2004-12-07 | Du Pont | Composto, composição e método para controle de pragas invertebradas |
| BR0311707A (pt) * | 2002-06-13 | 2005-03-15 | Du Pont | Composto, composição e método de controle de pelo menos uma praga invertebrada |
| MXPA05005025A (es) * | 2002-11-15 | 2005-08-03 | Du Pont | Nuevos insecticidas de antranilamida. |
| ES2424840T3 (es) | 2003-01-28 | 2013-10-09 | E.I. Du Pont De Nemours And Company | Insecticidas tipo ciano antranilamida |
| EP1631564A1 (en) * | 2003-06-12 | 2006-03-08 | E.I. Dupont De Nemours And Company | Method for preparing fused oxazinones |
| DE102004021564A1 (de) | 2003-11-14 | 2005-07-07 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| DE10353281A1 (de) | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
| DE10356550A1 (de) | 2003-12-04 | 2005-07-07 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
| US20070142327A1 (en) | 2003-12-04 | 2007-06-21 | Bayer Cropscience Aktiengesellschaft | Active compound combinations having insecticidal properties |
| KR20060135881A (ko) * | 2004-04-13 | 2006-12-29 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 안트라닐아미드 살충제 |
| GT200500179AA (es) | 2004-07-01 | 2008-10-29 | Mezclas sinergistas de agentes de antranilamida para el control de plagas de invertebrados | |
| DE102004035134A1 (de) | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von Halogenalkylnicotinsäurederivaten, Anthranilsäureamiden oder Phthalsäurediamiden und Safenern |
| MY140912A (en) * | 2004-07-26 | 2010-01-29 | Du Pont | Mixtures of anthranilamide invertebrate pest control agents |
| EP1789411A1 (en) * | 2004-08-17 | 2007-05-30 | E.I. Dupont De Nemours And Company | Novel anthranilamides useful for controlling invertebrate pests |
| AU2005306363B2 (en) * | 2004-11-18 | 2012-08-09 | E. I. Du Pont De Nemours And Company | Anthranilamide insecticides |
| TWI363756B (en) * | 2004-12-07 | 2012-05-11 | Du Pont | Method for preparing n-phenylpyrazole-1-carboxamides |
| AU2006283181A1 (en) * | 2005-08-24 | 2007-03-01 | E. I. Du Pont De Nemours And Company | Anthranilamides for controlling invertebrate pests |
| DE102005044108A1 (de) | 2005-09-15 | 2007-03-29 | Bayer Cropscience Ag | Dioxazin- und Oxdiazin-substituierte Arylamide |
| JP4587937B2 (ja) * | 2005-10-31 | 2010-11-24 | 日東電工株式会社 | スパイラル型分離膜エレメント |
| DE102006032168A1 (de) | 2006-06-13 | 2007-12-20 | Bayer Cropscience Ag | Anthranilsäurediamid-Derivate mit heteroaromatischen Substituenten |
| AU2008269144A1 (en) * | 2007-06-25 | 2008-12-31 | North Carolina State University | Compounds and compositions for the control of pests |
| US20090318393A1 (en) * | 2008-06-23 | 2009-12-24 | Shalaby Shalaby W | Film-forming liquid formulations for controlled release of pesticides |
| MX2011006319A (es) | 2008-12-18 | 2011-06-24 | Bayer Cropscience Ag | Amidas del acido antranilico sustituidas con tetrazol como plaguicidas. |
| BR112012019973B1 (pt) | 2010-02-09 | 2019-02-05 | Bayer Cropscience Ag | Derivados de ácido antranílico hidrazina-substituídos, misturas, compostos precursores,composições agroquímicas, processos para preparação dos referidos compostos e composições, uso dos compostos, das misturas ou das composições, e método para o controle de pragas animais |
| BR112012026523B1 (pt) | 2010-04-16 | 2018-11-27 | Bayer Intellectual Property Gmbh | antranilamidas substituídas com triazol, composições agroquímicas para controlar insetos prejudiciais e composições para controlar insetos prejudiciais as compreendendo, seu processo para preparar composições agroquímicas e uso, bem como método para controlar pragas animais ou fungos fitopatogênicos |
| CN103068820A (zh) | 2010-06-15 | 2013-04-24 | 拜耳知识产权有限责任公司 | 新的邻位取代的芳基酰胺衍生物 |
| CN103249729B (zh) | 2010-06-15 | 2017-04-05 | 拜耳知识产权有限责任公司 | 具有环状侧链的邻甲酰胺基苯甲酰胺衍生物 |
| CN103068814B (zh) | 2010-06-15 | 2015-11-25 | 拜耳知识产权有限责任公司 | 邻氨基苯甲酸衍生物 |
| MX2012014958A (es) | 2010-06-15 | 2013-02-12 | Bayer Ip Gmbh | Derivados de diamida antranilica. |
| CN102285971B (zh) * | 2010-06-21 | 2013-12-18 | 中国中化股份有限公司 | 吡唑基喹唑啉酮类化合物及其应用 |
| BR112013000583B1 (pt) | 2010-07-09 | 2018-06-12 | Bayer Intellectual Property Gmbh | Derivados de antranilamida como pesticidas, misturas dos referidos compostos, processo para preparar os compostos, composições, composições agroquímicas, processo para produzir as composições agroquímicas, uso do composto e método para controlar pragas animais |
| WO2012028578A1 (de) * | 2010-09-03 | 2012-03-08 | Bayer Cropscience Ag | Substituierte anellierte pyrimidinone und dihydropyrimidinone |
| CN102260245A (zh) * | 2011-06-02 | 2011-11-30 | 南开大学 | 2,3-二氢喹唑啉酮类衍生物及其制备方法和应用 |
| JP2014529618A (ja) * | 2011-09-02 | 2014-11-13 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | アリールキナゾリノン化合物を含む殺虫活性混合物 |
| WO2013092519A1 (en) | 2011-12-19 | 2013-06-27 | Bayer Cropscience Ag | Use of anthranilic acid diamide derivatives for pest control in transgenic crops |
| EP2606732A1 (en) | 2011-12-19 | 2013-06-26 | Bayer CropScience AG | Use of an anthranilic diamide derivatives with heteroaromatic and heterocyclic substituents in combination with a biological control agent |
| BR112015020830A2 (pt) | 2013-03-06 | 2017-07-18 | Bayer Cropscience Ag | diamidas de ácido antranílico substituídas com alcoximino como pesticidas |
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2003
- 2003-01-16 BR BR0307178-2A patent/BR0307178A/pt not_active Application Discontinuation
- 2003-01-16 JP JP2003562104A patent/JP4394953B2/ja not_active Expired - Lifetime
- 2003-01-16 US US10/496,724 patent/US7241767B2/en not_active Expired - Fee Related
- 2003-01-16 RU RU2004125582/04A patent/RU2315765C2/ru active
- 2003-01-16 ES ES03708845T patent/ES2427141T3/es not_active Expired - Lifetime
- 2003-01-16 EP EP03708845.7A patent/EP1467988B1/en not_active Expired - Lifetime
- 2003-01-16 WO PCT/US2003/001482 patent/WO2003062226A1/en not_active Ceased
- 2003-01-16 KR KR1020047011257A patent/KR101011837B1/ko not_active Expired - Fee Related
- 2003-01-16 MX MXPA04007018 patent/MX258385B/es active IP Right Grant
- 2003-01-16 CN CN03802557.4A patent/CN100349890C/zh not_active Expired - Fee Related
- 2003-01-16 CN CNA2007101529366A patent/CN101134755A/zh active Pending
- 2003-01-16 AU AU2003212811A patent/AU2003212811B2/en not_active Ceased
-
2004
- 2004-05-24 ZA ZA2004/04022A patent/ZA200404022B/en unknown
- 2004-07-20 MX MX2007014932A patent/MX283161B/es unknown
-
2006
- 2006-05-04 US US11/417,454 patent/US7683201B2/en not_active Expired - Lifetime
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2009
- 2009-07-16 AU AU2009202871A patent/AU2009202871B2/en not_active Expired
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