ZA200506245B - Pyrazole compounds - Google Patents
Pyrazole compounds Download PDFInfo
- Publication number
- ZA200506245B ZA200506245B ZA200506245A ZA200506245A ZA200506245B ZA 200506245 B ZA200506245 B ZA 200506245B ZA 200506245 A ZA200506245 A ZA 200506245A ZA 200506245 A ZA200506245 A ZA 200506245A ZA 200506245 B ZA200506245 B ZA 200506245B
- Authority
- ZA
- South Africa
- Prior art keywords
- alkyl
- formula
- pyrazole compound
- halogen
- hydrogen
- Prior art date
Links
- 150000003217 pyrazoles Chemical class 0.000 title description 4
- -1 pyrazole compound Chemical class 0.000 claims description 143
- 229910052739 hydrogen Inorganic materials 0.000 claims description 59
- 239000001257 hydrogen Substances 0.000 claims description 59
- 229910052736 halogen Inorganic materials 0.000 claims description 51
- 150000002367 halogens Chemical group 0.000 claims description 51
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 51
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 46
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 46
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 33
- 229910052801 chlorine Inorganic materials 0.000 claims description 33
- 239000000460 chlorine Substances 0.000 claims description 33
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 32
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 26
- 125000003342 alkenyl group Chemical group 0.000 claims description 24
- 125000000304 alkynyl group Chemical group 0.000 claims description 24
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 24
- 125000000262 haloalkenyl group Chemical group 0.000 claims description 24
- 125000000232 haloalkynyl group Chemical group 0.000 claims description 24
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 23
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 23
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 23
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 23
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 22
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims description 14
- 241000238421 Arthropoda Species 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 230000001473 noxious effect Effects 0.000 claims description 12
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000001301 oxygen Substances 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 125000001188 haloalkyl group Chemical group 0.000 claims description 9
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 description 34
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 16
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 230000001276 controlling effect Effects 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 2
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 2
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 description 1
- 125000006183 2,4-dimethyl benzyl group Chemical group [H]C1=C(C([H])=C(C(=C1[H])C([H])([H])*)C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000006280 2-bromobenzyl group Chemical group [H]C1=C([H])C(Br)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000000069 2-butynyl group Chemical group [H]C([H])([H])C#CC([H])([H])* 0.000 description 1
- 125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004847 2-fluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000006040 2-hexenyl group Chemical group 0.000 description 1
- 125000002927 2-methoxybenzyl group Chemical group [H]C1=C([H])C([H])=C(C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 description 1
- 125000006179 2-methyl benzyl group Chemical group [H]C1=C([H])C(=C(C([H])=C1[H])C([H])([H])*)C([H])([H])[H] 0.000 description 1
- 125000006022 2-methyl-2-propenyl group Chemical group 0.000 description 1
- 125000006024 2-pentenyl group Chemical group 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- 125000006186 3,5-dimethyl benzyl group Chemical group [H]C1=C(C([H])=C(C([H])=C1C([H])([H])[H])C([H])([H])*)C([H])([H])[H] 0.000 description 1
- 125000006279 3-bromobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Br)=C1[H])C([H])([H])* 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- 125000000474 3-butynyl group Chemical group [H]C#CC([H])([H])C([H])([H])* 0.000 description 1
- 125000003852 3-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Cl)=C1[H])C([H])([H])* 0.000 description 1
- 125000006284 3-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(F)=C1[H])C([H])([H])* 0.000 description 1
- 125000006041 3-hexenyl group Chemical group 0.000 description 1
- 125000006497 3-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 description 1
- 125000006180 3-methyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1[H])C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000005917 3-methylpentyl group Chemical group 0.000 description 1
- 125000006281 4-bromobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Br)C([H])([H])* 0.000 description 1
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
- 125000004176 4-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1F)C([H])([H])* 0.000 description 1
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000006181 4-methyl benzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000000173 4-trifluoromethoxy benzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC(F)(F)F)C([H])([H])* 0.000 description 1
- 125000001318 4-trifluoromethylbenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])*)C(F)(F)F 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (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)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003082385 | 2003-03-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200506245B true ZA200506245B (en) | 2007-09-26 |
Family
ID=33094917
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200506245A ZA200506245B (en) | 2003-03-25 | 2004-02-03 | Pyrazole compounds |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7442801B2 (ko) |
| EP (1) | EP1607390B1 (ko) |
| KR (1) | KR101021452B1 (ko) |
| CN (4) | CN1761654A (ko) |
| AT (1) | ATE481390T1 (ko) |
| AU (1) | AU2004224033B2 (ko) |
| BR (1) | BRPI0408755A (ko) |
| CO (1) | CO5611064A2 (ko) |
| DE (1) | DE602004029143D1 (ko) |
| EG (1) | EG24798A (ko) |
| ES (1) | ES2349635T3 (ko) |
| IL (1) | IL170056A (ko) |
| MX (1) | MXPA05010144A (ko) |
| PT (1) | PT1607390E (ko) |
| TW (1) | TW200505338A (ko) |
| WO (1) | WO2004085405A1 (ko) |
| ZA (1) | ZA200506245B (ko) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI344340B (en) | 2004-02-05 | 2011-07-01 | Sumitomo Chemical Co | Pyrazole compounds and use thereof |
| CN101747276B (zh) * | 2008-11-28 | 2011-09-07 | 中国中化股份有限公司 | 具有含氮五元杂环的醚类化合物及其应用 |
| JP2023547770A (ja) | 2020-09-25 | 2023-11-14 | ニューロポア セラピーズ インコーポレイテッド | Ｔｌｒシグナル伝達の調節剤としての化合物及び組成物 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6253970A (ja) | 1985-09-03 | 1987-03-09 | Nippon Nohyaku Co Ltd | ピラゾ−ル誘導体及びその製法 |
| US4843068A (en) * | 1985-12-27 | 1989-06-27 | Nihon Nohyaku Co., Ltd. | Pyrazole oxime derivatives and compositions |
| IL111252A0 (en) * | 1993-10-19 | 1994-12-29 | Sumitomo Chemical Co | Dihalopropene compound, insecticide/acaricide containing said dihalopropene compound as active ingredient,and intermediate compound for use in production of said dihalopropene compound |
| JPH08208551A (ja) * | 1995-02-01 | 1996-08-13 | Sumitomo Chem Co Ltd | ジハロプロペン化合物およびそれを有効成分とする殺虫、殺ダニ剤 |
| CN1072211C (zh) | 1997-01-23 | 2001-10-03 | 化学工业部沈阳化工研究院 | 作为农用杀菌剂和杀虫杀螨的吡唑类化合物及其制剂 |
| AU5020400A (en) * | 1999-05-20 | 2000-12-12 | E.I. Du Pont De Nemours And Company | Heteroaryloxypyrimidine insecticides and acaricides |
| JP2001354659A (ja) * | 2000-06-13 | 2001-12-25 | Kureha Chem Ind Co Ltd | 新規ピラゾリン誘導体、その製造方法、及び有害生物防除剤 |
| DE10063865A1 (de) * | 2000-12-21 | 2002-06-27 | Bayer Ag | Verwendung von Pyrazoloximen als Parasitizide |
-
2004
- 2004-02-03 MX MXPA05010144A patent/MXPA05010144A/es active IP Right Grant
- 2004-02-03 ES ES04707666T patent/ES2349635T3/es not_active Expired - Lifetime
- 2004-02-03 CN CNA2004800076819A patent/CN1761654A/zh active Pending
- 2004-02-03 AT AT04707666T patent/ATE481390T1/de not_active IP Right Cessation
- 2004-02-03 KR KR1020057017673A patent/KR101021452B1/ko not_active IP Right Cessation
- 2004-02-03 ZA ZA200506245A patent/ZA200506245B/en unknown
- 2004-02-03 PT PT04707666T patent/PT1607390E/pt unknown
- 2004-02-03 CN CN200910141408A patent/CN101704784A/zh active Pending
- 2004-02-03 BR BRPI0408755-0A patent/BRPI0408755A/pt active Search and Examination
- 2004-02-03 DE DE602004029143T patent/DE602004029143D1/de not_active Expired - Lifetime
- 2004-02-03 WO PCT/JP2004/001071 patent/WO2004085405A1/ja active Application Filing
- 2004-02-03 EP EP04707666A patent/EP1607390B1/en not_active Expired - Lifetime
- 2004-02-03 US US10/545,066 patent/US7442801B2/en not_active Expired - Fee Related
- 2004-02-03 CN CN200910141409A patent/CN101712651A/zh active Pending
- 2004-02-03 AU AU2004224033A patent/AU2004224033B2/en not_active Ceased
- 2004-02-03 CN CN2009101414107A patent/CN101701010B/zh not_active Expired - Fee Related
- 2004-02-10 TW TW093103089A patent/TW200505338A/zh not_active IP Right Cessation
-
2005
- 2005-08-03 IL IL170056A patent/IL170056A/en not_active IP Right Cessation
- 2005-09-05 CO CO05088702A patent/CO5611064A2/es active IP Right Grant
- 2005-09-24 EG EGNA2005000569 patent/EG24798A/xx active
Also Published As
| Publication number | Publication date |
|---|---|
| AU2004224033A1 (en) | 2004-10-07 |
| IL170056A (en) | 2010-11-30 |
| CN101712651A (zh) | 2010-05-26 |
| US20060142367A1 (en) | 2006-06-29 |
| KR20050111609A (ko) | 2005-11-25 |
| CN1761654A (zh) | 2006-04-19 |
| EP1607390A4 (en) | 2008-03-26 |
| US7442801B2 (en) | 2008-10-28 |
| EP1607390A1 (en) | 2005-12-21 |
| CN101701010B (zh) | 2012-06-13 |
| ES2349635T3 (es) | 2011-01-07 |
| CO5611064A2 (es) | 2006-02-28 |
| EG24798A (en) | 2010-09-15 |
| MXPA05010144A (es) | 2005-11-16 |
| TW200505338A (en) | 2005-02-16 |
| KR101021452B1 (ko) | 2011-03-16 |
| TWI321036B (ko) | 2010-03-01 |
| CN101704784A (zh) | 2010-05-12 |
| DE602004029143D1 (en) | 2010-10-28 |
| WO2004085405A1 (ja) | 2004-10-07 |
| EP1607390B1 (en) | 2010-09-15 |
| BRPI0408755A (pt) | 2006-03-28 |
| ATE481390T1 (de) | 2010-10-15 |
| AU2004224033B2 (en) | 2009-10-22 |
| CN101701010A (zh) | 2010-05-05 |
| PT1607390E (pt) | 2010-10-12 |
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