JP2008507494A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2008507494A5 JP2008507494A5 JP2007521922A JP2007521922A JP2008507494A5 JP 2008507494 A5 JP2008507494 A5 JP 2008507494A5 JP 2007521922 A JP2007521922 A JP 2007521922A JP 2007521922 A JP2007521922 A JP 2007521922A JP 2008507494 A5 JP2008507494 A5 JP 2008507494A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- halogen atoms
- halogenoalkyl
- halogen
- 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.)
- Pending
Links
- 125000005843 halogen group Chemical group 0.000 claims description 102
- -1 formyloxy group Chemical group 0.000 claims description 55
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 9
- 125000003277 amino group Chemical group 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 6
- 125000001188 haloalkyl group Chemical group 0.000 claims description 6
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 6
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 4
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims description 4
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 4
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 4
- 125000004011 3 membered carbocyclic group Chemical group 0.000 claims description 4
- 125000001845 4 membered carbocyclic group Chemical group 0.000 claims description 4
- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims description 4
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims description 4
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 4
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 4
- 125000004647 alkyl sulfenyl group Chemical group 0.000 claims description 4
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 4
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 4
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000001544 thienyl group Chemical group 0.000 claims description 4
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 2
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 239000002184 metal Chemical class 0.000 claims description 2
- 229910052752 metalloid Inorganic materials 0.000 claims description 2
- 150000002738 metalloids Chemical class 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 15
- 238000000034 method Methods 0.000 claims 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 claims 2
- 239000002689 soil Substances 0.000 claims 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 1
- 241000233866 Fungi Species 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 235000013399 edible fruits Nutrition 0.000 claims 1
- 230000000855 fungicidal effect Effects 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 150000004678 hydrides Chemical class 0.000 claims 1
- 238000005984 hydrogenation reaction Methods 0.000 claims 1
- 230000003032 phytopathogenic effect Effects 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 230000001988 toxicity Effects 0.000 claims 1
- 231100000419 toxicity Toxicity 0.000 claims 1
- BDWAQSDWIAGNLC-UHFFFAOYSA-N n-(2-pyridin-3-ylethyl)formamide Chemical class O=CNCCC1=CC=CN=C1 BDWAQSDWIAGNLC-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04356136 | 2004-07-23 | ||
| PCT/EP2005/009191 WO2006008194A1 (en) | 2004-07-23 | 2005-07-21 | 3-pyridinylethylcarboxamide derivatives as fungicides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008507494A JP2008507494A (ja) | 2008-03-13 |
| JP2008507494A5 true JP2008507494A5 (enExample) | 2008-05-08 |
Family
ID=34931755
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007521922A Pending JP2008507494A (ja) | 2004-07-23 | 2005-07-21 | 殺菌剤としての３−ピリジニルエチルカルボキサミド誘導体 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20080096932A1 (enExample) |
| EP (1) | EP1773812A1 (enExample) |
| JP (1) | JP2008507494A (enExample) |
| WO (1) | WO2006008194A1 (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110207771A1 (en) * | 2006-06-08 | 2011-08-25 | Syngenta Crop Protection, Inc. | N-(l-alkyl-2-phenylethyl)-carboxamide derivatives and use thereof as fungicides |
| WO2007144174A1 (en) | 2006-06-16 | 2007-12-21 | Syngenta Participations Ag | Ethenyl carboxamide derivatives useful as microbiocides |
| EP1992617A1 (en) * | 2007-05-15 | 2008-11-19 | Syngeta Participations AG | Optically active ethyl amides |
| US10793515B2 (en) | 2008-03-19 | 2020-10-06 | Aurimmed Pharma, Inc. | Compounds advantageous in the treatment of central nervous system diseases and disorders |
| WO2009117515A2 (en) | 2008-03-19 | 2009-09-24 | Aurimmed Pharma, Inc. | Novel compounds advantageous in the treatment of central nervous system diseases and disorders |
| US20210130285A1 (en) | 2008-03-19 | 2021-05-06 | Aurimmed Pharma, Inc. | Novel compounds advantageous in the treatment of central nervous system diseases and disorders |
| US9212155B2 (en) | 2008-03-19 | 2015-12-15 | Aurimmed Pharma, Inc. | Compounds advantageous in the treatment of central nervous system diseases and disorders |
| WO2011151369A1 (en) | 2010-06-03 | 2011-12-08 | Bayer Cropscience Ag | N-[(het)arylethyl)] pyrazole(thio)carboxamides and their heterosubstituted analogues |
| US9290485B2 (en) | 2010-08-04 | 2016-03-22 | Novartis Ag | N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides |
| RU2609210C2 (ru) | 2010-12-23 | 2017-01-31 | Алектос Терапьютикс Инк. | Селективные ингибиторы гликозидазы и их применение |
| WO2012129651A1 (en) | 2011-03-31 | 2012-10-04 | Alectos Therapeutics Inc. | Selective glycosidase inhibitors and uses thereof |
| US9701693B2 (en) | 2011-06-27 | 2017-07-11 | Alectos Therapeutics Inc. | Selective glycosidase inhibitors and uses thereof |
| EP2589294A1 (en) | 2011-11-02 | 2013-05-08 | Bayer CropScience AG | Compounds with nematicidal activity |
| CN104023540A (zh) | 2011-11-02 | 2014-09-03 | 拜耳知识产权有限责任公司 | 具有杀线虫活性的化合物 |
| EP2589292A1 (en) | 2011-11-02 | 2013-05-08 | Bayer CropScience AG | Compounds with nematicidal activity |
| EP2606727A1 (en) | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | Compounds with nematicidal activity |
| EP2606728A1 (en) | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | Compounds with nematicidal activity |
| RU2608217C2 (ru) | 2011-11-02 | 2017-01-17 | Байер Интеллектуэль Проперти Гмбх | Соединения с нематоцидной активностью |
| EP2890676B1 (en) | 2012-08-31 | 2018-12-05 | Alectos Therapeutics Inc. | Glycosidase inhibitors and uses thereof |
| EP2890675A4 (en) | 2012-08-31 | 2016-01-13 | Alectos Therapeutics Inc | GLYCOSIDASE INHIBITORS AND USES THEREOF |
| KR20150079711A (ko) | 2012-10-31 | 2015-07-08 | 알렉토스 테라퓨틱스 인크. | 글리코시다아제 저해제 및 이의 용도 |
| UY35772A (es) | 2013-10-14 | 2015-05-29 | Bayer Cropscience Ag | Nuevos compuestos plaguicidas |
| WO2018116073A1 (en) * | 2016-12-21 | 2018-06-28 | Pi Industries Ltd. | 1, 2, 3-thiadiazole compounds and their use as crop protecting agent |
| JP7128189B2 (ja) * | 2016-12-21 | 2022-08-30 | 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 | ２－ピリジルエチルカルボキサミド誘導体を調製する方法 |
| CN108440444B (zh) * | 2018-05-17 | 2021-01-19 | 江苏再拓生物科技有限公司 | 一种2-甲基-4-三氟甲基-5-噻唑甲酰胺化合物 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE159938T1 (de) * | 1990-12-17 | 1997-11-15 | Sankyo Co | Pyrazolderivate mit herbizider wirkung, deren herstellung und verwendung |
| ATE270817T1 (de) * | 1999-08-18 | 2004-07-15 | Aventis Cropscience Gmbh | Fungizide |
| EP1513829A2 (en) * | 2002-06-14 | 2005-03-16 | Syngenta Participations AG | Nicotinoyl derivatives as herbicidal compounds |
| AU2003266316B2 (en) * | 2002-08-12 | 2007-10-25 | Bayer S.A.S. | Novel 2-pyridylethylbenzamide derivative |
-
2005
- 2005-07-21 JP JP2007521922A patent/JP2008507494A/ja active Pending
- 2005-07-21 US US11/572,366 patent/US20080096932A1/en not_active Abandoned
- 2005-07-21 EP EP05777362A patent/EP1773812A1/en not_active Withdrawn
- 2005-07-21 WO PCT/EP2005/009191 patent/WO2006008194A1/en not_active Ceased
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2008507494A5 (enExample) | ||
| JP6386035B2 (ja) | 金属酵素阻害剤化合物 | |
| JP2010534716A5 (enExample) | ||
| EP2018367B1 (en) | Novel microbiocides | |
| JP4769789B2 (ja) | ２−ピリジニルエチルカルボキサミド誘導体及びその殺菌剤としての使用 | |
| CA2516186A1 (en) | Pyridine derivatives as fungicidal compounds | |
| JP2018509418A5 (enExample) | ||
| AR056882A1 (es) | Derivados del fungicida n- cicloalquil- bencil- amida | |
| RU2009149497A (ru) | Фунгицид на основе гетероциклил-пиримидинил-аминопроизводных | |
| JP4931600B2 (ja) | ２−ピリジニルエチルカルボキサミド誘導体及び殺真菌剤としてのそれらの使用 | |
| AR113903A2 (es) | Derivados fungicidas de pirazol carboxamidas | |
| JP4774043B2 (ja) | 殺菌剤として有用な２−ピリジニルシクロアルキルカルボキサミド誘導体 | |
| CN101535275A (zh) | 哒嗪衍生物 | |
| JP2017523997A5 (enExample) | ||
| RU2010107281A (ru) | Фунгицидные производные n-6-членного конденсированного (гетеро)арилметилен-n-циклоалкилкарбоксамида | |
| JPH07507781A (ja) | 除草剤ピラゾール−（チオ）−カルボキサミド | |
| RU2013123035A (ru) | 1-(гетероциклический карбонил) 2-замещенные пирролидины | |
| JP2007514735A (ja) | 殺寄生虫剤としての置換アリールピラゾール類 | |
| ZA200604258B (en) | Herbicidal pyrimidines | |
| JP2007534721A (ja) | ２−ピリジニルシクロアルキルベンズアミド誘導体及びその殺菌剤としての使用 | |
| JP3025001B2 (ja) | 殺菌性化合物、その製造法及びそれを含有する殺菌剤組成物 | |
| JP3762949B2 (ja) | ブラシノステロイド生合成阻害剤 | |
| JPWO2023110664A5 (enExample) | ||
| JP2022507262A (ja) | 除草化合物 | |
| JPWO2006004062A1 (ja) | ２，６−ジクロロ−４−ピリジルメチルアミン誘導体および農園芸用病害防除剤 |