JP2005506341A5 - - Google Patents
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- Publication number
- JP2005506341A5 JP2005506341A5 JP2003535546A JP2003535546A JP2005506341A5 JP 2005506341 A5 JP2005506341 A5 JP 2005506341A5 JP 2003535546 A JP2003535546 A JP 2003535546A JP 2003535546 A JP2003535546 A JP 2003535546A JP 2005506341 A5 JP2005506341 A5 JP 2005506341A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- independently
- chloro
- alkoxy
- halogen
- 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
- 229910052799 carbon Inorganic materials 0.000 claims 25
- 229910052736 halogen Inorganic materials 0.000 claims 24
- 150000002367 halogens Chemical class 0.000 claims 24
- -1 C 1 -C 4 alkoxy Chemical group 0.000 claims 21
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 19
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 18
- 125000001424 substituent group Chemical group 0.000 claims 15
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 14
- 150000001875 compounds Chemical class 0.000 claims 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 12
- 125000001072 heteroaryl group Chemical group 0.000 claims 11
- 229910052739 hydrogen Inorganic materials 0.000 claims 11
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 10
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 10
- 125000004663 dialkyl amino group Chemical group 0.000 claims 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 7
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000000262 haloalkenyl group Chemical group 0.000 claims 5
- 238000000034 method Methods 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 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 125000004473 dialkylaminocarbonyl group Chemical group 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
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 241000607479 Yersinia pestis Species 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims 2
- 150000001204 N-oxides Chemical class 0.000 claims 2
- 229910052789 astatine Inorganic materials 0.000 claims 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 229910052740 iodine Inorganic materials 0.000 claims 2
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical group C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 2
- LGHATAABPWJILK-UHFFFAOYSA-N 2-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazol-3-yl]-8-methyl-n-propan-2-yl-3,1-benzoxazin-4-imine Chemical compound N=1C2=C(C)C=CC=C2C(=NC(C)C)OC=1C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl LGHATAABPWJILK-UHFFFAOYSA-N 0.000 claims 1
- VQBJVERORJHCCN-UHFFFAOYSA-N 2-[5-bromo-2-(3-chloropyridin-2-yl)pyrazol-3-yl]-6-chloro-8-methyl-n-propan-2-yl-3,1-benzoxazin-4-imine Chemical compound N=1C2=C(C)C=C(Cl)C=C2C(=NC(C)C)OC=1C1=CC(Br)=NN1C1=NC=CC=C1Cl VQBJVERORJHCCN-UHFFFAOYSA-N 0.000 claims 1
- PBMPZEQGCZRCOJ-UHFFFAOYSA-N 2-[5-bromo-2-(3-chloropyridin-2-yl)pyrazol-3-yl]-8-methyl-n-propan-2-yl-3,1-benzoxazin-4-imine Chemical compound N=1C2=C(C)C=CC=C2C(=NC(C)C)OC=1C1=CC(Br)=NN1C1=NC=CC=C1Cl PBMPZEQGCZRCOJ-UHFFFAOYSA-N 0.000 claims 1
- BJUPQUWZTOPDNZ-UHFFFAOYSA-N 2-[5-bromo-2-(3-chloropyridin-2-yl)pyrazol-3-yl]-n-tert-butyl-8-methyl-3,1-benzoxazin-4-imine Chemical compound CC1=CC=CC(C(O2)=NC(C)(C)C)=C1N=C2C1=CC(Br)=NN1C1=NC=CC=C1Cl BJUPQUWZTOPDNZ-UHFFFAOYSA-N 0.000 claims 1
- LGIKLOQGMRLUBW-UHFFFAOYSA-N 6-chloro-2-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazol-3-yl]-8-methyl-n-propan-2-yl-3,1-benzoxazin-4-imine Chemical compound N=1C2=C(C)C=C(Cl)C=C2C(=NC(C)C)OC=1C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl LGIKLOQGMRLUBW-UHFFFAOYSA-N 0.000 claims 1
- CRYCGVUSMMFXPQ-UHFFFAOYSA-N 6-chloro-2-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazol-3-yl]-n,8-dimethyl-3,1-benzoxazin-4-imine Chemical compound N=1C2=C(C)C=C(Cl)C=C2C(=NC)OC=1C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl CRYCGVUSMMFXPQ-UHFFFAOYSA-N 0.000 claims 1
- DEFDNYDOZUXEMX-UHFFFAOYSA-N 6-chloro-2-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazol-3-yl]-n-ethyl-8-methyl-3,1-benzoxazin-4-imine Chemical compound N=1C2=C(C)C=C(Cl)C=C2C(=NCC)OC=1C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl DEFDNYDOZUXEMX-UHFFFAOYSA-N 0.000 claims 1
- ADIYMGNJUFSKBW-UHFFFAOYSA-N 6-chloro-2-[5-chloro-2-(3-chloropyridin-2-yl)pyrazol-3-yl]-8-methyl-n-propan-2-yl-3,1-benzoxazin-4-imine Chemical compound N=1C2=C(C)C=C(Cl)C=C2C(=NC(C)C)OC=1C1=CC(Cl)=NN1C1=NC=CC=C1Cl ADIYMGNJUFSKBW-UHFFFAOYSA-N 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- ORCDYENSSHCORS-UHFFFAOYSA-N n-tert-butyl-6-chloro-2-[2-(3-chloropyridin-2-yl)-5-(trifluoromethyl)pyrazol-3-yl]-8-methyl-3,1-benzoxazin-4-imine Chemical compound CC1=CC(Cl)=CC(C(O2)=NC(C)(C)C)=C1N=C2C1=CC(C(F)(F)F)=NN1C1=NC=CC=C1Cl ORCDYENSSHCORS-UHFFFAOYSA-N 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32939201P | 2001-10-15 | 2001-10-15 | |
| PCT/US2002/032845 WO2003032731A1 (en) | 2001-10-15 | 2002-10-15 | Iminobenzoxazines, iminobenzthiazines and iminoquinazolines for controlling invertebrate pests |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005506341A JP2005506341A (ja) | 2005-03-03 |
| JP2005506341A5 true JP2005506341A5 (cg-RX-API-DMAC10.html) | 2005-12-22 |
| JP4317752B2 JP4317752B2 (ja) | 2009-08-19 |
Family
ID=23285170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003535546A Expired - Fee Related JP4317752B2 (ja) | 2001-10-15 | 2002-10-15 | 無脊椎害虫を防除するためのイミノベンゾオキサジン、イミノベンズチアジンおよびイミノキナゾリン |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US7148217B2 (cg-RX-API-DMAC10.html) |
| EP (1) | EP1435785B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP4317752B2 (cg-RX-API-DMAC10.html) |
| KR (1) | KR100840083B1 (cg-RX-API-DMAC10.html) |
| CN (1) | CN100503604C (cg-RX-API-DMAC10.html) |
| AU (1) | AU2002343512B2 (cg-RX-API-DMAC10.html) |
| BR (1) | BR0213646A (cg-RX-API-DMAC10.html) |
| DE (1) | DE60230651D1 (cg-RX-API-DMAC10.html) |
| ES (1) | ES2319972T3 (cg-RX-API-DMAC10.html) |
| MX (1) | MXPA04003445A (cg-RX-API-DMAC10.html) |
| RU (1) | RU2298007C2 (cg-RX-API-DMAC10.html) |
| WO (1) | WO2003032731A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| MY142967A (en) | 2001-08-13 | 2011-01-31 | Du Pont | Method for controlling particular insect pests by applying anthranilamide compounds |
| TW200724033A (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
| CN100349890C (zh) * | 2002-01-22 | 2007-11-21 | 纳幕尔杜邦公司 | 用于防治无脊椎害虫的喹唑啉(二)酮 |
| CN100335477C (zh) * | 2002-06-13 | 2007-09-05 | 纳幕尔杜邦公司 | 吡唑甲酰胺杀虫剂 |
| AU2003295491B2 (en) * | 2002-11-15 | 2009-10-08 | E.I. Du Pont De Nemours And Company | Novel anthranilamide insecticides |
| CL2004000234A1 (es) * | 2003-02-12 | 2005-04-15 | Biogen Idec Inc | Compuestos derivados 3-(piridin-2-il)-4-heteroaril-pirazol sustituidos, antagonistas de aik5 y/o aik4; composicion farmaceutica y uso del compuesto en el tratamiento de desordenes fibroticos como esclerodermia, lupus nefritico, cicatrizacion de herid |
| BRPI0515221A (pt) * | 2004-08-17 | 2008-07-15 | Du Pont | composto, composição para controlar uma peste invertebrada, composições spray e de isca, dispositivo de armadilha, métodos para controlar uma peste invertebrada e métodos de controle |
| 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 |
| EP1924575A1 (en) * | 2005-08-24 | 2008-05-28 | E.I.Du pont de nemours and company | Anthranilamides for controlling invertebrate pests |
| EP2008521A1 (en) * | 2007-06-28 | 2008-12-31 | Syngeta Participations AG | Methods of controlling insects |
| US8110608B2 (en) | 2008-06-05 | 2012-02-07 | Ecolab Usa Inc. | Solid form sodium lauryl sulfate (SLS) pesticide composition |
| US20090318393A1 (en) * | 2008-06-23 | 2009-12-24 | Shalaby Shalaby W | Film-forming liquid formulations for controlled release of pesticides |
| RU2555404C2 (ru) * | 2010-04-27 | 2015-07-10 | Сумитомо Кемикал Компани, Лимитед | Пестицидная композиция и способ борьбы с вредителями |
| JP5712504B2 (ja) | 2010-04-27 | 2015-05-07 | 住友化学株式会社 | 有害生物防除組成物およびその用途 |
| WO2011135828A1 (en) | 2010-04-27 | 2011-11-03 | Sumitomo Chemical Company, Limited | Pesticidal composition and its use |
| PL2563135T3 (pl) | 2010-04-28 | 2017-06-30 | Sumitomo Chemical Company, Limited | Kompozycja do kontrolowania chorób roślin i jej zastosowanie |
| NZ603844A (en) * | 2010-04-28 | 2014-08-29 | Sumitomo Chemical Co | Pesticidal composition and its use |
| JP5789918B2 (ja) * | 2010-04-28 | 2015-10-07 | 住友化学株式会社 | 植物病害防除組成物およびその用途 |
| JP5724211B2 (ja) | 2010-04-28 | 2015-05-27 | 住友化学株式会社 | 植物病害防除組成物およびその用途 |
| RU2572758C2 (ru) * | 2010-07-20 | 2016-01-20 | Байер Интеллектуэль Проперти Гмбх | Гелевая приманка для борьбы с ползающими вредными насекомыми |
| US8968757B2 (en) | 2010-10-12 | 2015-03-03 | Ecolab Usa Inc. | Highly wettable, water dispersible, granules including two pesticides |
| JP6457942B2 (ja) * | 2012-10-05 | 2019-01-23 | ライジェル ファーマシューティカルズ， インコーポレイテッド | Ｇｄｆ−８阻害剤 |
| WO2018019765A1 (en) * | 2016-07-27 | 2018-02-01 | Basf Se | Herbicidal pyrimidine compounds |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4146718A (en) * | 1978-04-10 | 1979-03-27 | Bristol-Myers Company | Alkyl 5,6-dichloro-3,4-dihydro-2(1h)-iminoquinazoline-3-acetate hydrohalides |
| DE2934543A1 (de) | 1979-08-27 | 1981-04-02 | Basf Ag, 6700 Ludwigshafen | Substituierte n-benzoylanthranilsaeurederivate und deren anydroverbindungen, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
| NO179282C (no) * | 1991-01-18 | 1996-09-11 | Rhone Poulenc Agrochimie | Nye 1-(2-pyridyl)pyrazolforbindelser til kontroll av skadeinsekter |
| NL9202078A (nl) | 1992-11-30 | 1994-06-16 | Rijkslandbouwhogeschool | Nieuwe N-acyl-antranilzuurverbindingen en toepassing van N-acyl-antranilzuurverbindingen bij de bestrijding van insecten. |
| US5602126A (en) | 1993-11-22 | 1997-02-11 | E. I. Du Pont De Nemours And Company | Arthropodicidal anilides |
| WO1995018116A1 (en) | 1993-12-29 | 1995-07-06 | E.I. Du Pont De Nemours And Company | Arthropodicidal oxadiazine-, thiadiazine- or triazine-carboxanilides |
| DE4428380A1 (de) | 1994-08-11 | 1996-02-15 | Bayer Ag | 4-Trifluormethylbenzamide |
| WO1996038419A1 (en) | 1995-05-31 | 1996-12-05 | Nissan Chemical Industries, Ltd. | 5-pyrazolecarboxamide derivatives and plant disease control agent |
| TW515786B (en) | 1997-11-25 | 2003-01-01 | Nihon Nohyaku Co Ltd | Phthalic acid diamide derivatives, agricultural and horticultural insecticides, and a method for application of the insecticides |
| DE19840322A1 (de) | 1998-09-04 | 2000-03-09 | Bayer Ag | Pyrazol-carboxanilide |
| GT199900185A (es) * | 1998-11-06 | 2001-04-18 | Novedosa pirimidin-4-enamina como fungicida. | |
| AU780574B2 (en) * | 1999-04-15 | 2005-04-07 | Devgen N.V. | Compound screening method |
| AR030154A1 (es) | 1999-07-05 | 2003-08-13 | Nihon Nohyaku Co Ltd | Derivado de ftalamida, derivado de amina heterociclico util como intermediario para la produccion del mismo, insecticida agrohorticola y metodo para utilizar dicho insecticida |
| EP1226123A1 (en) | 1999-11-03 | 2002-07-31 | Du Pont Pharmaceuticals Company | Cyano compounds as factor xa inhibitors |
| MY138097A (en) | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
-
2002
- 2002-10-15 KR KR1020047005481A patent/KR100840083B1/ko not_active Expired - Fee Related
- 2002-10-15 US US10/488,233 patent/US7148217B2/en not_active Expired - Fee Related
- 2002-10-15 CN CNB028203585A patent/CN100503604C/zh not_active Expired - Fee Related
- 2002-10-15 EP EP02780457A patent/EP1435785B1/en not_active Expired - Lifetime
- 2002-10-15 AU AU2002343512A patent/AU2002343512B2/en not_active Ceased
- 2002-10-15 JP JP2003535546A patent/JP4317752B2/ja not_active Expired - Fee Related
- 2002-10-15 WO PCT/US2002/032845 patent/WO2003032731A1/en not_active Ceased
- 2002-10-15 ES ES02780457T patent/ES2319972T3/es not_active Expired - Lifetime
- 2002-10-15 DE DE60230651T patent/DE60230651D1/de not_active Expired - Lifetime
- 2002-10-15 MX MXPA04003445A patent/MXPA04003445A/es not_active Application Discontinuation
- 2002-10-15 BR BR0213646-5A patent/BR0213646A/pt not_active Application Discontinuation
- 2002-10-15 RU RU2004114856/04A patent/RU2298007C2/ru not_active IP Right Cessation
-
2006
- 2006-07-21 US US11/490,898 patent/US7326704B2/en not_active Expired - Fee Related
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