JP2013505901A5 - - Google Patents
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- JP2013505901A5 JP2013505901A5 JP2012530156A JP2012530156A JP2013505901A5 JP 2013505901 A5 JP2013505901 A5 JP 2013505901A5 JP 2012530156 A JP2012530156 A JP 2012530156A JP 2012530156 A JP2012530156 A JP 2012530156A JP 2013505901 A5 JP2013505901 A5 JP 2013505901A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- cor
- halogen
- alkenyl
- 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.)
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 141
- -1 cyano, nitro, methyl sulfenyl Chemical group 0.000 claims description 132
- 229910052736 halogen Inorganic materials 0.000 claims description 46
- 150000002367 halogens Chemical group 0.000 claims description 40
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 30
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 30
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 24
- 239000001257 hydrogen Substances 0.000 claims description 24
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 22
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 13
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 12
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 101100440696 Caenorhabditis elegans cor-1 gene Proteins 0.000 claims description 11
- 125000000623 heterocyclic group Chemical group 0.000 claims description 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 8
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 8
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 8
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 claims description 8
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims description 8
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims description 8
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 8
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 claims description 6
- HNJBEVLQSNELDL-UHFFFAOYSA-N gamma-butyrolactam Natural products O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 6
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims description 4
- 125000001766 1,2,4-oxadiazol-3-yl group Chemical group [H]C1=NC(*)=NO1 0.000 claims description 4
- 125000001305 1,2,4-triazol-3-yl group Chemical group [H]N1N=C([*])N=C1[H] 0.000 claims description 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
- 125000004284 isoxazol-3-yl group Chemical group [H]C1=C([H])C(*)=NO1 0.000 claims description 4
- 125000004287 oxazol-2-yl group Chemical group [H]C1=C([H])N=C(*)O1 0.000 claims description 4
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims description 2
- 125000001724 1,2,3-oxadiazol-4-yl group Chemical group [H]C1=C(*)N=NO1 0.000 claims description 2
- 125000004503 1,2,3-oxadiazol-5-yl group Chemical group O1N=NC=C1* 0.000 claims description 2
- 125000004512 1,2,3-thiadiazol-4-yl group Chemical group S1N=NC(=C1)* 0.000 claims description 2
- 125000001359 1,2,3-triazol-4-yl group Chemical group [H]N1N=NC([*])=C1[H] 0.000 claims description 2
- 125000001506 1,2,3-triazol-5-yl group Chemical group [H]N1N=NC([H])=C1[*] 0.000 claims description 2
- 125000004505 1,2,4-oxadiazol-5-yl group Chemical group O1N=CN=C1* 0.000 claims description 2
- 125000004515 1,2,4-thiadiazol-3-yl group Chemical group S1N=C(N=C1)* 0.000 claims description 2
- 125000004516 1,2,4-thiadiazol-5-yl group Chemical group S1N=CN=C1* 0.000 claims description 2
- 125000001414 1,2,4-triazol-5-yl group Chemical group [H]N1N=C([H])N=C1[*] 0.000 claims description 2
- 125000004507 1,2,5-oxadiazol-3-yl group Chemical group O1N=C(C=N1)* 0.000 claims description 2
- 125000004518 1,2,5-thiadiazol-3-yl group Chemical group S1N=C(C=N1)* 0.000 claims description 2
- 125000004521 1,3,4-thiadiazol-2-yl group Chemical group S1C(=NN=C1)* 0.000 claims description 2
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
- 230000001548 androgenic effect Effects 0.000 claims description 2
- 125000003037 imidazol-2-yl group Chemical group [H]N1C([*])=NC([H])=C1[H] 0.000 claims description 2
- 125000002140 imidazol-4-yl group Chemical group [H]N1C([H])=NC([*])=C1[H] 0.000 claims description 2
- 125000000336 imidazol-5-yl group Chemical group [H]N1C([H])=NC([H])=C1[*] 0.000 claims description 2
- 125000001793 isothiazol-3-yl group Chemical group [H]C1=C([H])C(*)=NS1 0.000 claims description 2
- 125000004500 isothiazol-4-yl group Chemical group S1N=CC(=C1)* 0.000 claims description 2
- 125000004501 isothiazol-5-yl group Chemical group S1N=CC=C1* 0.000 claims description 2
- 125000004498 isoxazol-4-yl group Chemical group O1N=CC(=C1)* 0.000 claims description 2
- 125000004499 isoxazol-5-yl group Chemical group O1N=CC=C1* 0.000 claims description 2
- 125000003145 oxazol-4-yl group Chemical group O1C=NC(=C1)* 0.000 claims description 2
- 125000004304 oxazol-5-yl group Chemical group O1C=NC=C1* 0.000 claims description 2
- 125000004574 piperidin-2-yl group Chemical group N1C(CCCC1)* 0.000 claims description 2
- 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 claims description 2
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims description 2
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 2
- 125000004289 pyrazol-3-yl group Chemical group [H]N1N=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 claims description 2
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims description 2
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 2
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims description 2
- 125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 claims description 2
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 claims description 2
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 9
- 230000002363 herbicidal effect Effects 0.000 claims 8
- 244000038559 crop plants Species 0.000 claims 2
- 239000004009 herbicide Substances 0.000 claims 2
- 230000000895 acaricidal effect Effects 0.000 claims 1
- 239000000642 acaricide Substances 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 230000009261 transgenic effect Effects 0.000 claims 1
- 244000045561 useful plants Species 0.000 claims 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09012169 | 2009-09-25 | ||
| EP09012169.0 | 2009-09-25 | ||
| US24629509P | 2009-09-28 | 2009-09-28 | |
| US61/246,295 | 2009-09-28 | ||
| PCT/EP2010/005739 WO2011035874A1 (de) | 2009-09-25 | 2010-09-18 | N-(1,2,5-oxadiazol-3-yl)benzamide und ihre verwendung als herbizide |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013505901A JP2013505901A (ja) | 2013-02-21 |
| JP2013505901A5 true JP2013505901A5 (OSRAM) | 2015-03-26 |
| JP5728480B2 JP5728480B2 (ja) | 2015-06-03 |
Family
ID=41557691
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012530156A Active JP5728480B2 (ja) | 2009-09-25 | 2010-09-18 | Ｎ−（１，２，５−オキサジアゾール−３−イル）ベンズアミド類および除草剤としてのそれの使用 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US8288316B2 (OSRAM) |
| EP (1) | EP2480539B1 (OSRAM) |
| JP (1) | JP5728480B2 (OSRAM) |
| CN (1) | CN102639517B (OSRAM) |
| AR (1) | AR078312A1 (OSRAM) |
| AU (1) | AU2010297635B2 (OSRAM) |
| BR (1) | BR112012007442B1 (OSRAM) |
| CA (1) | CA2775104C (OSRAM) |
| ES (1) | ES2428104T3 (OSRAM) |
| IN (1) | IN2012DN03057A (OSRAM) |
| MX (1) | MX2012003377A (OSRAM) |
| PL (1) | PL2480539T3 (OSRAM) |
| RU (1) | RU2554349C9 (OSRAM) |
| UA (1) | UA107672C2 (OSRAM) |
| WO (1) | WO2011035874A1 (OSRAM) |
Families Citing this family (102)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8097712B2 (en) | 2007-11-07 | 2012-01-17 | Beelogics Inc. | Compositions for conferring tolerance to viral disease in social insects, and the use thereof |
| US8962584B2 (en) | 2009-10-14 | 2015-02-24 | Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. | Compositions for controlling Varroa mites in bees |
| CN102822350B (zh) | 2010-03-08 | 2015-05-06 | 孟山都技术公司 | 用于植物基因调控的多核苷酸分子 |
| WO2012123420A1 (de) * | 2011-03-15 | 2012-09-20 | Bayer Cropscience Ag | Herbizid-safener-zusammensetzungen |
| JP6008881B2 (ja) * | 2011-03-15 | 2016-10-19 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | Ｎ−（１，２，５−オキサジアゾール−３−イル）ピリジンカルボキサミド類及び除草剤としてのそれらの使用 |
| AU2012228355B2 (en) | 2011-03-15 | 2016-09-22 | Bayer Cropscience Aktiengesellschaft | N-(1,2,5-oxadiazol-3-yl)-, N-(tetrazol-5-yl)- and N-(triazol-5-yl)bicycloarylcarboxamides and their use as herbicides |
| JP5847920B2 (ja) * | 2011-03-25 | 2016-01-27 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | Ｈｐｐｄインヒビター除草剤に対して耐性であるトランスジェニック作物植物の領域において望まぬ植物を制御するためのｎ−（１，２，５−オキサジアゾール−３−イル）ベンズアミドの使用 |
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| AU2012331283A1 (en) * | 2011-11-03 | 2014-05-22 | Bayer Intellectual Property Gmbh | Herbicidally active oxime-ether-substituted benzoylamides |
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| CN104125949B (zh) * | 2012-02-21 | 2016-04-13 | 拜耳知识产权有限责任公司 | 除草的3-(亚磺酰亚氨基/磺酰亚氨基)-苯甲酰胺 |
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| JP6310936B2 (ja) * | 2012-12-07 | 2018-04-11 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | Ｎ−（イソオキサゾール−３−イル）−アリール−カルボン酸アミド類及び除草剤としてのそれらの使用 |
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| IT1196237B (it) * | 1984-08-29 | 1988-11-16 | Enichimica Secondaria | Composti eterociclici ad attivita' erbicida |
| SE0102764D0 (sv) * | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
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-
2010
- 2010-09-18 MX MX2012003377A patent/MX2012003377A/es active IP Right Grant
- 2010-09-18 WO PCT/EP2010/005739 patent/WO2011035874A1/de not_active Ceased
- 2010-09-18 PL PL10754896T patent/PL2480539T3/pl unknown
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