RU2306310C2 - Замещенные тиазолилом карбоциклические 1,3-дионы в качестве средств для борьбы с вредителями - Google Patents
Замещенные тиазолилом карбоциклические 1,3-дионы в качестве средств для борьбы с вредителями Download PDFInfo
- Publication number
- RU2306310C2 RU2306310C2 RU2003133144/04A RU2003133144A RU2306310C2 RU 2306310 C2 RU2306310 C2 RU 2306310C2 RU 2003133144/04 A RU2003133144/04 A RU 2003133144/04A RU 2003133144 A RU2003133144 A RU 2003133144A RU 2306310 C2 RU2306310 C2 RU 2306310C2
- Authority
- RU
- Russia
- Prior art keywords
- carbon atoms
- hydrogen
- alkyl
- mean
- oxygen
- Prior art date
Links
- 241000607479 Yersinia pestis Species 0.000 title abstract 2
- 125000002837 carbocyclic group Chemical class 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 56
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 42
- 239000001257 hydrogen Substances 0.000 claims abstract 42
- 229910052799 carbon Inorganic materials 0.000 claims abstract 12
- 150000001875 compounds Chemical class 0.000 claims abstract 5
- 125000003118 aryl group Chemical group 0.000 claims abstract 2
- 150000002431 hydrogen Chemical class 0.000 claims 29
- 125000000217 alkyl group Chemical group 0.000 claims 27
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 18
- 229910052760 oxygen Inorganic materials 0.000 claims 18
- 239000001301 oxygen Substances 0.000 claims 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 15
- 150000001721 carbon Chemical group 0.000 claims 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 10
- 229910052801 chlorine Inorganic materials 0.000 claims 10
- 239000000460 chlorine Substances 0.000 claims 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 7
- 229910052731 fluorine Inorganic materials 0.000 claims 7
- 239000011737 fluorine Substances 0.000 claims 7
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 7
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 7
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 5
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 239000011593 sulfur Substances 0.000 claims 5
- 229910052717 sulfur Inorganic materials 0.000 claims 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 125000001153 fluoro group Chemical group F* 0.000 claims 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 4
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- -1 chloro, phenyl Chemical group 0.000 claims 2
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- SQQWBSBBCSFQGC-JLHYYAGUSA-N ubiquinone-2 Chemical compound COC1=C(OC)C(=O)C(C\C=C(/C)CCC=C(C)C)=C(C)C1=O SQQWBSBBCSFQGC-JLHYYAGUSA-N 0.000 claims 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Health & Medical Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10118310A DE10118310A1 (de) | 2001-04-12 | 2001-04-12 | Hetarylsubstituierte carbocyclische 1,3-Dione |
| DE10118310.0 | 2001-04-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2003133144A RU2003133144A (ru) | 2005-05-10 |
| RU2306310C2 true RU2306310C2 (ru) | 2007-09-20 |
Family
ID=7681383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2003133144/04A RU2306310C2 (ru) | 2001-04-12 | 2002-04-02 | Замещенные тиазолилом карбоциклические 1,3-дионы в качестве средств для борьбы с вредителями |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7595404B2 (enExample) |
| EP (1) | EP1381596B1 (enExample) |
| JP (1) | JP4413497B2 (enExample) |
| KR (1) | KR100862892B1 (enExample) |
| CN (2) | CN1272329C (enExample) |
| AR (1) | AR035454A1 (enExample) |
| AT (1) | ATE340787T1 (enExample) |
| BR (1) | BR0209082B1 (enExample) |
| CA (1) | CA2443642C (enExample) |
| DE (2) | DE10118310A1 (enExample) |
| DK (1) | DK1381596T3 (enExample) |
| ES (1) | ES2271332T3 (enExample) |
| MX (1) | MXPA03009315A (enExample) |
| PL (1) | PL364391A1 (enExample) |
| RU (1) | RU2306310C2 (enExample) |
| UA (1) | UA76749C2 (enExample) |
| WO (1) | WO2002088098A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7338969B2 (en) * | 2002-03-08 | 2008-03-04 | Quonova, Llc | Modulation of pathogenicity |
| DE10331675A1 (de) * | 2003-07-14 | 2005-02-10 | Bayer Cropscience Ag | Hetarylsubstituierte Pyrazolidindion-Derivate |
| GB0704652D0 (en) * | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| GB0712653D0 (en) | 2007-06-28 | 2007-08-08 | Syngenta Ltd | Novel herbicides |
| GB0714981D0 (en) * | 2007-08-01 | 2007-09-12 | Syngenta Ltd | Novel herbicides |
| GB0717082D0 (en) | 2007-09-03 | 2007-10-10 | Syngenta Ltd | Novel herbicides |
| GB0819205D0 (en) | 2008-10-20 | 2008-11-26 | Syngenta Ltd | Novel herbicides |
| US9051300B2 (en) * | 2009-07-31 | 2015-06-09 | Syngenta Limited | Herbicides |
| CN103857661B (zh) * | 2011-08-11 | 2016-11-16 | 拜耳知识产权有限责任公司 | 1,2,4‑三唑基取代的酮烯醇 |
| IL310022B2 (en) * | 2021-07-12 | 2024-11-01 | Fortephest Ltd | Novel derivatives of non-coded amino acids and their use as herbicides |
| CN116196314B (zh) * | 2023-05-04 | 2023-08-15 | 广州市妇女儿童医疗中心 | Ri-1或其盐在制备防治胃肠道疾病的药物中的应用 |
| CN116589393A (zh) * | 2023-05-19 | 2023-08-15 | 开封博凯生物化工有限公司 | 以二正丁胺为缚酸剂生产溴虫腈的工艺 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1567300A (en) * | 1977-03-28 | 1980-05-14 | Union Carbide Corp | Synthesis of biocidal 2-aryl-1,3-cycloalkane-diones and their enol esters |
| US4659372A (en) * | 1977-03-28 | 1987-04-21 | Union Carbide Corporation | Biocidal 2-aryl-1,3-cyclohexanedione enol ester compounds |
| EP0368592A1 (en) * | 1988-11-07 | 1990-05-16 | Imperial Chemical Industries Plc | Herbicidal compositions |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL130759C (enExample) * | 1965-10-07 | |||
| CN1003445B (zh) * | 1984-10-03 | 1989-03-01 | 武田药品工业株式会社 | 噻唑烷二酮衍生物，其制备方法和用途 |
-
2001
- 2001-04-12 DE DE10118310A patent/DE10118310A1/de not_active Withdrawn
-
2002
- 2002-02-04 UA UA20031110185A patent/UA76749C2/uk unknown
- 2002-04-02 JP JP2002585400A patent/JP4413497B2/ja not_active Expired - Fee Related
- 2002-04-02 KR KR1020037013128A patent/KR100862892B1/ko not_active Expired - Fee Related
- 2002-04-02 CN CNB028116569A patent/CN1272329C/zh not_active Expired - Fee Related
- 2002-04-02 BR BRPI0209082-1A patent/BR0209082B1/pt not_active IP Right Cessation
- 2002-04-02 AT AT02766566T patent/ATE340787T1/de not_active IP Right Cessation
- 2002-04-02 ES ES02766566T patent/ES2271332T3/es not_active Expired - Lifetime
- 2002-04-02 PL PL02364391A patent/PL364391A1/xx not_active Application Discontinuation
- 2002-04-02 DE DE50208258T patent/DE50208258D1/de not_active Expired - Lifetime
- 2002-04-02 CN CNB2006100956330A patent/CN100537551C/zh not_active Expired - Fee Related
- 2002-04-02 US US10/474,308 patent/US7595404B2/en not_active Expired - Fee Related
- 2002-04-02 DK DK02766566T patent/DK1381596T3/da active
- 2002-04-02 MX MXPA03009315A patent/MXPA03009315A/es active IP Right Grant
- 2002-04-02 WO PCT/EP2002/003620 patent/WO2002088098A1/de not_active Ceased
- 2002-04-02 CA CA2443642A patent/CA2443642C/en not_active Expired - Fee Related
- 2002-04-02 RU RU2003133144/04A patent/RU2306310C2/ru not_active IP Right Cessation
- 2002-04-02 EP EP02766566A patent/EP1381596B1/de not_active Expired - Lifetime
- 2002-04-05 AR ARP020101269A patent/AR035454A1/es not_active Application Discontinuation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1567300A (en) * | 1977-03-28 | 1980-05-14 | Union Carbide Corp | Synthesis of biocidal 2-aryl-1,3-cycloalkane-diones and their enol esters |
| US4659372A (en) * | 1977-03-28 | 1987-04-21 | Union Carbide Corporation | Biocidal 2-aryl-1,3-cyclohexanedione enol ester compounds |
| EP0368592A1 (en) * | 1988-11-07 | 1990-05-16 | Imperial Chemical Industries Plc | Herbicidal compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2443642A1 (en) | 2002-11-07 |
| DE10118310A1 (de) | 2002-10-17 |
| UA76749C2 (uk) | 2006-09-15 |
| CN100537551C (zh) | 2009-09-09 |
| CN1880308A (zh) | 2006-12-20 |
| EP1381596B1 (de) | 2006-09-27 |
| CN1272329C (zh) | 2006-08-30 |
| RU2003133144A (ru) | 2005-05-10 |
| ATE340787T1 (de) | 2006-10-15 |
| AR035454A1 (es) | 2004-05-26 |
| PL364391A1 (en) | 2004-12-13 |
| KR100862892B1 (ko) | 2008-10-13 |
| DE50208258D1 (de) | 2006-11-09 |
| ES2271332T3 (es) | 2007-04-16 |
| JP4413497B2 (ja) | 2010-02-10 |
| CA2443642C (en) | 2011-03-08 |
| EP1381596A1 (de) | 2004-01-21 |
| US20070135630A1 (en) | 2007-06-14 |
| MXPA03009315A (es) | 2004-02-12 |
| KR20040067869A (ko) | 2004-07-30 |
| DK1381596T3 (da) | 2007-02-05 |
| WO2002088098A1 (de) | 2002-11-07 |
| BR0209082A (pt) | 2004-08-10 |
| CN1514830A (zh) | 2004-07-21 |
| BR0209082B1 (pt) | 2014-10-07 |
| US7595404B2 (en) | 2009-09-29 |
| JP2004528350A (ja) | 2004-09-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20110403 |