RU2004130832A - Бициклические конденсированные пиридиниламиды и преимущественные композиции на их основе для использования в качестве фунгицидов - Google Patents
Бициклические конденсированные пиридиниламиды и преимущественные композиции на их основе для использования в качестве фунгицидов Download PDFInfo
- Publication number
- RU2004130832A RU2004130832A RU2004130832/04A RU2004130832A RU2004130832A RU 2004130832 A RU2004130832 A RU 2004130832A RU 2004130832/04 A RU2004130832/04 A RU 2004130832/04A RU 2004130832 A RU2004130832 A RU 2004130832A RU 2004130832 A RU2004130832 A RU 2004130832A
- Authority
- RU
- Russia
- Prior art keywords
- compound according
- halogen
- group
- fused
- haloalkoxy
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims 8
- 239000000417 fungicide Substances 0.000 title claims 5
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical class NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 title 1
- 125000002619 bicyclic group Chemical group 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 19
- 229910052736 halogen Inorganic materials 0.000 claims 10
- 150000002367 halogens Chemical class 0.000 claims 10
- -1 C 1 -C 4 alkoxy Chemical group 0.000 claims 6
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 5
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 4
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 4
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims 3
- 230000000855 fungicidal effect Effects 0.000 claims 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 229930182558 Sterol Natural products 0.000 claims 2
- 230000015572 biosynthetic process Effects 0.000 claims 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 244000000004 fungal plant pathogen Species 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 150000003432 sterols Chemical class 0.000 claims 2
- 235000003702 sterols Nutrition 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 claims 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- BBCAHRBPRAIHNL-UHFFFAOYSA-N 2,4-dichloro-n-[[3-chloro-5-(trifluoromethyl)pyridin-2-yl]methyl]-5,6,7,8-tetrahydroquinoline-3-carboxamide Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CNC(=O)C1=C(Cl)N=C(CCCC2)C2=C1Cl BBCAHRBPRAIHNL-UHFFFAOYSA-N 0.000 claims 1
- FGZONTDHYXDWJJ-UHFFFAOYSA-N 3-bromo-n-[1-(5-bromo-3-chloropyridin-2-yl)ethyl]isoquinoline-4-carboxamide Chemical compound BrC=1N=CC2=CC=CC=C2C=1C(=O)NC(C)C1=NC=C(Br)C=C1Cl FGZONTDHYXDWJJ-UHFFFAOYSA-N 0.000 claims 1
- YCIPQJTZJGUXND-UHFFFAOYSA-N Aglaia odorata Alkaloid Natural products C1=CC(OC)=CC=C1C1(C(C=2C(=O)N3CCCC3=NC=22)C=3C=CC=CC=3)C2(O)C2=C(OC)C=C(OC)C=C2O1 YCIPQJTZJGUXND-UHFFFAOYSA-N 0.000 claims 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 1
- 239000005756 Cymoxanil Substances 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 101000615488 Homo sapiens Methyl-CpG-binding domain protein 2 Proteins 0.000 claims 1
- 102100021299 Methyl-CpG-binding domain protein 2 Human genes 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 claims 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 1
- 239000012990 dithiocarbamate Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 230000002538 fungal effect Effects 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 230000002438 mitochondrial effect Effects 0.000 claims 1
- FGKZFRZCDYHPJY-UHFFFAOYSA-N n-[1-(5-bromo-3-chloropyridin-2-yl)ethyl]-3-fluoroisoquinoline-4-carboxamide Chemical compound FC=1N=CC2=CC=CC=C2C=1C(=O)NC(C)C1=NC=C(Br)C=C1Cl FGKZFRZCDYHPJY-UHFFFAOYSA-N 0.000 claims 1
- 125000005543 phthalimide group Chemical class 0.000 claims 1
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims 1
- 230000000241 respiratory effect Effects 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000007787 solid Substances 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36576702P | 2002-03-19 | 2002-03-19 | |
| US60/365,767 | 2002-03-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2004130832A true RU2004130832A (ru) | 2005-04-10 |
Family
ID=28454714
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2004130832/04A RU2004130832A (ru) | 2002-03-19 | 2003-02-20 | Бициклические конденсированные пиридиниламиды и преимущественные композиции на их основе для использования в качестве фунгицидов |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20050020644A1 (enExample) |
| EP (1) | EP1485372A2 (enExample) |
| JP (1) | JP2005526100A (enExample) |
| CN (1) | CN1642940A (enExample) |
| AR (1) | AR039028A1 (enExample) |
| AU (1) | AU2003216364A1 (enExample) |
| BR (1) | BR0308458A (enExample) |
| IL (1) | IL162892A0 (enExample) |
| MX (1) | MXPA04009002A (enExample) |
| PL (1) | PL372988A1 (enExample) |
| RU (1) | RU2004130832A (enExample) |
| TW (1) | TW200306159A (enExample) |
| WO (1) | WO2003080596A2 (enExample) |
| ZA (1) | ZA200405643B (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200407075A (en) * | 2002-03-19 | 2004-05-16 | Du Pont | Pyridinyl amides and advantageous compositions thereof for use as fungicides |
| JP2009542599A (ja) * | 2006-07-06 | 2009-12-03 | バイエル・クロツプサイエンス・エス・アー | 防かび剤としてのｎ−［（ピリジン−２−イル）メトキシ］複素環式カルボキサミド誘導体及び関連化合物 |
| WO2008059370A2 (en) | 2006-11-17 | 2008-05-22 | Pfizer Japan Inc. | Substituted bicyclocarboxyamide compounds |
| JP2009114178A (ja) * | 2007-10-15 | 2009-05-28 | Sumitomo Chemical Co Ltd | アミド化合物及びその植物病害防除用途 |
| JP2009120587A (ja) * | 2007-10-23 | 2009-06-04 | Sumitomo Chemical Co Ltd | アミド化合物及びその用途 |
| CN102448937A (zh) * | 2009-05-29 | 2012-05-09 | 拉夸里亚创药株式会社 | 作为钙或钠通道阻滞剂的芳基取代羧酰胺衍生物 |
| RU2535671C1 (ru) * | 2010-10-18 | 2014-12-20 | Раквалиа Фарма Инк. | Производные ариламидов в качестве блокаторов ttx-s |
| WO2013003315A2 (en) * | 2011-06-26 | 2013-01-03 | President And Fellows Of Harvard College | Methods for preparing isoquinolines |
| BR112017023448A2 (pt) * | 2015-04-29 | 2018-07-31 | The State Of Israel, Ministry Of Agriculture & Rural Development, Agricultural Research Organization (Aro) (Volcani Center) | composições anti-fitopatogênicas |
| ES2894762T3 (es) * | 2017-09-13 | 2022-02-15 | Syngenta Participations Ag | Derivados de quinolina (tio)carboxamida microbiocidas |
| CN111050558B (zh) * | 2017-09-13 | 2022-05-27 | 先正达参股股份有限公司 | 杀微生物的喹啉(硫代)羧酰胺衍生物 |
| BR112020004933A2 (pt) * | 2017-09-13 | 2020-09-15 | Syngenta Participations Ag | derivados microbiocidas de (tio)carboxamida de quinolina |
| WO2021063736A1 (en) * | 2019-10-02 | 2021-04-08 | Basf Se | Bicyclic pyridine derivatives |
| WO2022150962A1 (en) * | 2021-01-12 | 2022-07-21 | Westlake Pharmaceutical (Hangzhou) Co., Ltd. | Protease inhibitors, preparation, and uses thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1228691A3 (de) * | 1997-12-18 | 2002-08-14 | Basf Aktiengesellschaft | Fungizide Mischungen auf der Basis von Pyridincarboxamidverbindungen |
| GB9919588D0 (en) * | 1999-08-18 | 1999-10-20 | Hoechst Schering Agrevo Gmbh | Fungicidal compounds |
| EP1322614A2 (en) * | 2000-09-18 | 2003-07-02 | E. I. du Pont de Nemours and Company | Pyridinyl amides and imides for use as fungicides |
-
2003
- 2003-02-19 TW TW092103415A patent/TW200306159A/zh unknown
- 2003-02-20 WO PCT/US2003/005383 patent/WO2003080596A2/en not_active Ceased
- 2003-02-20 PL PL03372988A patent/PL372988A1/xx not_active Application Discontinuation
- 2003-02-20 MX MXPA04009002A patent/MXPA04009002A/es unknown
- 2003-02-20 CN CN03806571.1A patent/CN1642940A/zh active Pending
- 2003-02-20 EP EP03745079A patent/EP1485372A2/en not_active Withdrawn
- 2003-02-20 BR BR0308458-2A patent/BR0308458A/pt not_active IP Right Cessation
- 2003-02-20 AU AU2003216364A patent/AU2003216364A1/en not_active Abandoned
- 2003-02-20 IL IL16289203A patent/IL162892A0/xx unknown
- 2003-02-20 JP JP2003578350A patent/JP2005526100A/ja not_active Withdrawn
- 2003-02-20 RU RU2004130832/04A patent/RU2004130832A/ru not_active Application Discontinuation
- 2003-02-20 US US10/501,258 patent/US20050020644A1/en not_active Abandoned
- 2003-03-19 AR ARP030100969A patent/AR039028A1/es not_active Application Discontinuation
-
2004
- 2004-07-15 ZA ZA200405643A patent/ZA200405643B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2003216364A1 (en) | 2003-10-08 |
| CN1642940A (zh) | 2005-07-20 |
| JP2005526100A (ja) | 2005-09-02 |
| WO2003080596A2 (en) | 2003-10-02 |
| TW200306159A (en) | 2003-11-16 |
| US20050020644A1 (en) | 2005-01-27 |
| IL162892A0 (en) | 2005-11-20 |
| AU2003216364A8 (en) | 2003-10-08 |
| EP1485372A2 (en) | 2004-12-15 |
| AR039028A1 (es) | 2005-02-02 |
| MXPA04009002A (es) | 2004-12-07 |
| BR0308458A (pt) | 2005-01-18 |
| ZA200405643B (en) | 2005-07-15 |
| WO2003080596A3 (en) | 2004-04-01 |
| PL372988A1 (en) | 2005-08-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA92 | Acknowledgement of application withdrawn (lack of supplementary materials submitted) |
Effective date: 20070214 |