JP2006515288A5 - - Google Patents
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- Publication number
- JP2006515288A5 JP2006515288A5 JP2004556132A JP2004556132A JP2006515288A5 JP 2006515288 A5 JP2006515288 A5 JP 2006515288A5 JP 2004556132 A JP2004556132 A JP 2004556132A JP 2004556132 A JP2004556132 A JP 2004556132A JP 2006515288 A5 JP2006515288 A5 JP 2006515288A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- formula
- compound
- cycloalkyl
- haloalkyl
- 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
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 40
- 229910052736 halogen Inorganic materials 0.000 claims description 16
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 15
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 12
- 150000002367 halogens Chemical class 0.000 claims description 11
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 6
- 125000001475 halogen functional group Chemical group 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- -1 R 5 is H Chemical group 0.000 claims description 3
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 3
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 3
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 31
- 150000003839 salts Chemical class 0.000 claims 17
- 125000005843 halogen group Chemical group 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 3
- 230000010933 acylation Effects 0.000 claims 3
- 238000005917 acylation reaction Methods 0.000 claims 3
- 230000029936 alkylation Effects 0.000 claims 3
- 238000005804 alkylation reaction Methods 0.000 claims 3
- 125000001072 heteroaryl group Chemical group 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 230000006103 sulfonylation Effects 0.000 claims 3
- 238000005694 sulfonylation reaction Methods 0.000 claims 3
- 125000006414 CCl Chemical group ClC* 0.000 claims 2
- 241000607479 Yersinia pestis Species 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 125000002541 furyl group Chemical group 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 125000004306 triazinyl group Chemical group 0.000 claims 2
- 125000001425 triazolyl group Chemical group 0.000 claims 2
- 239000000273 veterinary drug Substances 0.000 claims 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 239000003905 agrochemical Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 0 *CCC(C=C(*)C=C(C*)C1)=C1[n]1nc(C(N(*)*)=N*)c(*)c1N(*)C=* Chemical compound *CCC(C=C(*)C=C(C*)C1)=C1[n]1nc(C(N(*)*)=N*)c(*)c1N(*)C=* 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02027064 | 2002-12-03 | ||
| EP02027064.1 | 2002-12-03 | ||
| PCT/EP2003/012620 WO2004050633A1 (en) | 2002-12-03 | 2003-11-12 | Pesticidal 1-ayl-3-amidoxime-pyrazole derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006515288A JP2006515288A (ja) | 2006-05-25 |
| JP2006515288A5 true JP2006515288A5 (enExample) | 2006-09-14 |
| JP4839463B2 JP4839463B2 (ja) | 2011-12-21 |
Family
ID=32405693
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004556132A Expired - Fee Related JP4839463B2 (ja) | 2002-12-03 | 2003-11-12 | 農薬としての１−アリール−３−アミドキシム−ピラゾール誘導体 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7514428B2 (enExample) |
| EP (1) | EP1599451B1 (enExample) |
| JP (1) | JP4839463B2 (enExample) |
| KR (1) | KR101146546B1 (enExample) |
| CN (1) | CN100408565C (enExample) |
| AR (1) | AR042256A1 (enExample) |
| AU (1) | AU2003289709B2 (enExample) |
| BR (2) | BR0316996B1 (enExample) |
| CA (1) | CA2508330C (enExample) |
| CO (1) | CO5690508A2 (enExample) |
| EA (1) | EA009644B1 (enExample) |
| ES (1) | ES2417016T3 (enExample) |
| MX (1) | MXPA05005900A (enExample) |
| NZ (1) | NZ540463A (enExample) |
| WO (1) | WO2004050633A1 (enExample) |
| ZA (1) | ZA200503744B (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5041536B2 (ja) * | 2004-12-07 | 2012-10-03 | メリアル リミテッド | 農薬化合物としての５−アミノピラゾール誘導体 |
| WO2006125641A2 (en) * | 2005-05-25 | 2006-11-30 | Basf Aktiengesellschaft | Pyridine compounds for combating arthropod pests and nematodes |
| DE102006014653A1 (de) * | 2006-03-28 | 2007-10-04 | Bayer Cropscience Ag | Verwendung von Tetramsäurederivaten zur Bekämpfung von Insekten durch Angiessen, Tröpfchenapplikation oder Bodeninjektion |
| UA120354C2 (uk) | 2013-09-30 | 2019-11-25 | Фмк Корпорейшн | Піноутворювальний препарат і пристрій для доставки |
| AR100936A1 (es) | 2014-06-24 | 2016-11-09 | Fmc Corp | Formulaciones de espumas y concentrados emulsionables |
| AU2016378184B2 (en) | 2015-12-23 | 2022-04-21 | Fmc Corporation | In situ treatment of seed in furrow |
| CN108148049B (zh) * | 2018-01-17 | 2020-03-10 | 河北大学 | 一种三嗪酮结构的5-吡唑酰胺类化合物制备方法与应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4631211A (en) | 1985-03-25 | 1986-12-23 | Scripps Clinic & Research Foundation | Means for sequential solid phase organic synthesis and methods using the same |
| GB8713768D0 (en) * | 1987-06-12 | 1987-07-15 | May & Baker Ltd | Compositions of matter |
| NO179282C (no) * | 1991-01-18 | 1996-09-11 | Rhone Poulenc Agrochimie | Nye 1-(2-pyridyl)pyrazolforbindelser til kontroll av skadeinsekter |
| BR9408026A (pt) * | 1993-11-09 | 1996-12-17 | Idemitsu Kosan Co | Derivados de pirazol e herbicidas contendo os mesmos |
| CN1167683C (zh) * | 1996-01-30 | 2004-09-22 | 住化武田农药株式会社 | 芳基吡唑化合物、其制备方法、含其的农药组合物及其用途 |
| US6350771B1 (en) * | 1996-12-24 | 2002-02-26 | Rhone-Poulenc, Inc. | Pesticidal 1-arylpyrazoles |
| ZA9711534B (en) * | 1996-12-24 | 1998-06-24 | Rhone Poulenc Agrochimie | Pesticidal 1-arylpyrazoles. |
| ZA981776B (en) * | 1997-03-10 | 1998-09-03 | Rhone Poulenc Agrochimie | Pesticidal 1-arylpyrazoles |
| ZA200601794B (en) * | 2003-09-04 | 2007-04-25 | Bayer Cropscience Sa | Pesticidal 5-substituted-oxyalkylamino-1-arylpyrazole derivatives |
-
2003
- 2003-11-12 BR BRPI0316996-0B1A patent/BR0316996B1/pt active IP Right Grant
- 2003-11-12 BR BRPI0316996A patent/BRPI0316996B8/pt not_active IP Right Cessation
- 2003-11-12 AU AU2003289709A patent/AU2003289709B2/en not_active Ceased
- 2003-11-12 EA EA200500931A patent/EA009644B1/ru not_active IP Right Cessation
- 2003-11-12 KR KR1020057009949A patent/KR101146546B1/ko not_active Expired - Fee Related
- 2003-11-12 WO PCT/EP2003/012620 patent/WO2004050633A1/en not_active Ceased
- 2003-11-12 CN CNB2003801048582A patent/CN100408565C/zh not_active Expired - Fee Related
- 2003-11-12 NZ NZ540463A patent/NZ540463A/en not_active IP Right Cessation
- 2003-11-12 ES ES03779896T patent/ES2417016T3/es not_active Expired - Lifetime
- 2003-11-12 JP JP2004556132A patent/JP4839463B2/ja not_active Expired - Fee Related
- 2003-11-12 EP EP03779896.4A patent/EP1599451B1/en not_active Expired - Lifetime
- 2003-11-12 CA CA2508330A patent/CA2508330C/en not_active Expired - Fee Related
- 2003-11-12 US US10/537,466 patent/US7514428B2/en not_active Expired - Lifetime
- 2003-11-12 MX MXPA05005900A patent/MXPA05005900A/es active IP Right Grant
- 2003-12-01 AR ARP030104422A patent/AR042256A1/es not_active Application Discontinuation
-
2005
- 2005-05-10 ZA ZA200503744A patent/ZA200503744B/en unknown
- 2005-05-31 CO CO05052702A patent/CO5690508A2/es active IP Right Grant
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