TW200407075A - Pyridinyl amides and advantageous compositions thereof for use as fungicides - Google Patents
Pyridinyl amides and advantageous compositions thereof for use as fungicides Download PDFInfo
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- TW200407075A TW200407075A TW092104247A TW92104247A TW200407075A TW 200407075 A TW200407075 A TW 200407075A TW 092104247 A TW092104247 A TW 092104247A TW 92104247 A TW92104247 A TW 92104247A TW 200407075 A TW200407075 A TW 200407075A
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- 239000000203 mixture Substances 0.000 title claims abstract description 133
- 239000000417 fungicide Substances 0.000 title claims abstract description 43
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical class NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 148
- 201000010099 disease Diseases 0.000 claims abstract description 49
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 49
- 238000000034 method Methods 0.000 claims abstract description 16
- 229930182558 Sterol Natural products 0.000 claims abstract description 14
- 150000003432 sterols Chemical class 0.000 claims abstract description 14
- 235000003702 sterols Nutrition 0.000 claims abstract description 14
- 230000002538 fungal effect Effects 0.000 claims abstract description 8
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000001204 N-oxides Chemical class 0.000 claims abstract description 6
- 230000002438 mitochondrial effect Effects 0.000 claims abstract description 6
- 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 abstract description 5
- 230000000241 respiratory effect Effects 0.000 claims abstract description 5
- 230000027756 respiratory electron transport chain Effects 0.000 claims abstract description 4
- 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 abstract 2
- 239000005756 Cymoxanil Substances 0.000 claims abstract 2
- 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 abstract 2
- -1 C2-C6 li fast Chemical group 0.000 claims description 74
- 241000196324 Embryophyta Species 0.000 claims description 35
- 230000000855 fungicidal effect Effects 0.000 claims description 18
- 240000006365 Vitis vinifera Species 0.000 claims description 15
- 235000014787 Vitis vinifera Nutrition 0.000 claims description 15
- 230000015572 biosynthetic process Effects 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 235000009754 Vitis X bourquina Nutrition 0.000 claims description 13
- 235000012333 Vitis X labruscana Nutrition 0.000 claims description 13
- 244000052769 pathogen Species 0.000 claims description 12
- 235000007688 Lycopersicon esculentum Nutrition 0.000 claims description 10
- 240000003768 Solanum lycopersicum Species 0.000 claims description 10
- WJZHMLNIAZSFDO-UHFFFAOYSA-N manganese zinc Chemical compound [Mn].[Zn] WJZHMLNIAZSFDO-UHFFFAOYSA-N 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 230000001717 pathogenic effect Effects 0.000 claims description 8
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- 125000001188 haloalkyl group Chemical group 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 125000004414 alkyl thio group Chemical group 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 125000003282 alkyl amino group Chemical group 0.000 claims description 5
- 125000000304 alkynyl group Chemical group 0.000 claims description 5
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 4
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
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- 125000005347 halocycloalkyl group Chemical group 0.000 claims description 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
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- 239000005772 Famoxadone Substances 0.000 claims description 2
- 239000005802 Mancozeb Substances 0.000 claims description 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 2
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- 150000003431 steroids Chemical class 0.000 claims description 2
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 claims 1
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
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- 229940025084 amphetamine Drugs 0.000 claims 1
- 230000001195 anabolic effect Effects 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 230000017858 demethylation Effects 0.000 claims 1
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- 244000053095 fungal pathogen Species 0.000 claims 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 1
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- 101000615488 Homo sapiens Methyl-CpG-binding domain protein 2 Proteins 0.000 abstract description 5
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- 150000003053 piperidines Chemical class 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 242
- 238000012360 testing method Methods 0.000 description 65
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- OPFJDXRVMFKJJO-ZHHKINOHSA-N N-{[3-(2-benzamido-4-methyl-1,3-thiazol-5-yl)-pyrazol-5-yl]carbonyl}-G-dR-G-dD-dD-dD-NH2 Chemical compound S1C(C=2NN=C(C=2)C(=O)NCC(=O)N[C@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(N)=O)=C(C)N=C1NC(=O)C1=CC=CC=C1 OPFJDXRVMFKJJO-ZHHKINOHSA-N 0.000 description 23
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- 239000000243 solution Substances 0.000 description 23
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- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 18
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- 125000004354 sulfur functional group Chemical group 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000005936 tau-Fluvalinate Substances 0.000 description 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 229940035936 ubiquinone Drugs 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229940011671 vitamin b6 Drugs 0.000 description 1
- 235000019386 wax ester Nutrition 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 229940118149 zinc sulfate monohydrate Drugs 0.000 description 1
- RNZCSKGULNFAMC-UHFFFAOYSA-L zinc;hydrogen sulfate;hydroxide Chemical compound O.[Zn+2].[O-]S([O-])(=O)=O RNZCSKGULNFAMC-UHFFFAOYSA-L 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Information Transfer Between Computers (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36576602P | 2002-03-19 | 2002-03-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW200407075A true TW200407075A (en) | 2004-05-16 |
Family
ID=28454713
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW092104247A TW200407075A (en) | 2002-03-19 | 2003-02-27 | Pyridinyl amides and advantageous compositions thereof for use as fungicides |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20050009889A1 (enExample) |
| EP (1) | EP1484969A1 (enExample) |
| JP (1) | JP2005520838A (enExample) |
| CN (1) | CN1665395A (enExample) |
| AR (1) | AR039030A1 (enExample) |
| AU (1) | AU2003220358A1 (enExample) |
| BR (1) | BR0308459A (enExample) |
| IL (1) | IL162894A0 (enExample) |
| MX (1) | MXPA04009000A (enExample) |
| PL (1) | PL372569A1 (enExample) |
| RU (1) | RU2004130839A (enExample) |
| TW (1) | TW200407075A (enExample) |
| WO (1) | WO2003079787A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200306155A (en) * | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
| DE10248335A1 (de) | 2002-10-17 | 2004-05-06 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| FR2928070A1 (fr) * | 2008-02-27 | 2009-09-04 | Sumitomo Chemical Co | Composition agricole, utilisation d'un compose pour sa production et procede pour matriser ou prevenir les maladies des plantes. |
| US9302991B2 (en) | 2010-10-18 | 2016-04-05 | Raqualia Pharma Inc. | Arylamide derivatives as TTX-S blockers |
| CN102084865B (zh) * | 2011-03-25 | 2013-10-30 | 陕西先农生物科技有限公司 | 粉唑醇·丙森锌杀菌组合物 |
| JP2017206440A (ja) * | 2014-09-10 | 2017-11-24 | 日本曹達株式会社 | ピリジン化合物およびその用途 |
| US12376898B2 (en) | 2016-07-01 | 2025-08-05 | Cynosure, Llc | Non-invasive, uniform and non-uniform RF methods and systems related applications |
| WO2020070049A1 (en) * | 2018-10-02 | 2020-04-09 | Syngenta Participations Ag | Pesticidally active benzene- and azine-amide compounds |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0710841A (ja) * | 1993-06-21 | 1995-01-13 | Ishihara Sangyo Kaisha Ltd | 4−トリフルオロメチルピリジン−3−カルボキサミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 |
| JPH0725853A (ja) * | 1993-07-14 | 1995-01-27 | Ishihara Sangyo Kaisha Ltd | アミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 |
| DE59806215D1 (de) * | 1997-12-18 | 2002-12-12 | Basf Ag | Fungizide mischungen auf der basis von amidverbindungen |
| GB9919588D0 (en) * | 1999-08-18 | 1999-10-20 | Hoechst Schering Agrevo Gmbh | Fungicidal compounds |
| AU2002211233A1 (en) * | 2000-09-18 | 2002-03-26 | E.I. Du Pont De Nemours And Company | Pyridinyl amides and imides for use as fungicides |
| TW200306159A (en) * | 2002-03-19 | 2003-11-16 | Du Pont | Bicyclic fused pyridinyl amides and advantageous compositions thereof for use as fungicides |
-
2003
- 2003-02-27 TW TW092104247A patent/TW200407075A/zh unknown
- 2003-03-18 CN CN03806453.7A patent/CN1665395A/zh active Pending
- 2003-03-18 JP JP2003577630A patent/JP2005520838A/ja not_active Withdrawn
- 2003-03-18 IL IL16289403A patent/IL162894A0/xx unknown
- 2003-03-18 RU RU2004130839/04A patent/RU2004130839A/ru not_active Application Discontinuation
- 2003-03-18 WO PCT/US2003/008186 patent/WO2003079787A1/en not_active Ceased
- 2003-03-18 PL PL03372569A patent/PL372569A1/xx not_active Application Discontinuation
- 2003-03-18 MX MXPA04009000A patent/MXPA04009000A/es unknown
- 2003-03-18 BR BR0308459-0A patent/BR0308459A/pt not_active IP Right Cessation
- 2003-03-18 EP EP03716658A patent/EP1484969A1/en not_active Withdrawn
- 2003-03-18 AU AU2003220358A patent/AU2003220358A1/en not_active Abandoned
- 2003-03-18 US US10/501,853 patent/US20050009889A1/en not_active Abandoned
- 2003-03-19 AR ARP030100971A patent/AR039030A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1484969A1 (en) | 2004-12-15 |
| US20050009889A1 (en) | 2005-01-13 |
| PL372569A1 (en) | 2005-07-25 |
| WO2003079787A9 (en) | 2004-02-12 |
| RU2004130839A (ru) | 2005-04-10 |
| AU2003220358A1 (en) | 2003-10-08 |
| WO2003079787A1 (en) | 2003-10-02 |
| MXPA04009000A (es) | 2004-12-07 |
| BR0308459A (pt) | 2005-01-18 |
| JP2005520838A (ja) | 2005-07-14 |
| CN1665395A (zh) | 2005-09-07 |
| AR039030A1 (es) | 2005-02-02 |
| IL162894A0 (en) | 2005-11-20 |
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