JP2002529450A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2002529450A5 JP2002529450A5 JP2000580992A JP2000580992A JP2002529450A5 JP 2002529450 A5 JP2002529450 A5 JP 2002529450A5 JP 2000580992 A JP2000580992 A JP 2000580992A JP 2000580992 A JP2000580992 A JP 2000580992A JP 2002529450 A5 JP2002529450 A5 JP 2002529450A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- optionally
- phenyl
- alkoxy
- substituted
- 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.)
- Withdrawn
Links
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 25
- 229910052739 hydrogen Inorganic materials 0.000 description 21
- 239000001257 hydrogen Substances 0.000 description 21
- 229910052736 halogen Inorganic materials 0.000 description 16
- 150000002367 halogens Chemical class 0.000 description 16
- 229910052760 oxygen Inorganic materials 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 13
- 239000001301 oxygen Substances 0.000 description 13
- 125000004093 cyano group Chemical group *C#N 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- 150000002431 hydrogen Chemical class 0.000 description 10
- 229910052717 sulfur Chemical group 0.000 description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 8
- 239000011593 sulfur Chemical group 0.000 description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
- 239000011737 fluorine Substances 0.000 description 7
- 229910052731 fluorine Inorganic materials 0.000 description 7
- 125000001072 heteroaryl group Chemical group 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 125000001153 fluoro group Chemical group F* 0.000 description 5
- 125000000547 substituted alkyl group Chemical group 0.000 description 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 125000005842 heteroatom Chemical group 0.000 description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 125000003884 phenylalkyl group Chemical group 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 description 2
- 241000790917 Dioxys <bee> Species 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- -1 phenoxy, benzyloxy Chemical group 0.000 description 2
- 125000006413 ring segment Chemical group 0.000 description 2
- 125000000335 thiazolyl group Chemical group 0.000 description 2
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 description 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 description 1
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 description 1
- CYVFHNCRFJQILT-UHFFFAOYSA-N 5-(3,4-dimethoxyphenyl)pyrrolidine-2-thione Chemical class C1=C(OC)C(OC)=CC=C1C1NC(=S)CC1 CYVFHNCRFJQILT-UHFFFAOYSA-N 0.000 description 1
- GUCFLOJYYAMVPQ-UHFFFAOYSA-N 5-phenylpyrrolidine-2-thione Chemical compound N1C(=S)CCC1C1=CC=CC=C1 GUCFLOJYYAMVPQ-UHFFFAOYSA-N 0.000 description 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 description 1
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241001553014 Myrsine salicina Species 0.000 description 1
- YUWFDIPZXPGFBD-UHFFFAOYSA-N N#CC(C1NCCC1)C(c1ccccc1Cl)=O Chemical compound N#CC(C1NCCC1)C(c1ccccc1Cl)=O YUWFDIPZXPGFBD-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000005620 boronic acid group Chemical class 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 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 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003624 transition metals Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19851986A DE19851986A1 (de) | 1998-11-11 | 1998-11-11 | Phenyl-substituierte zyklische Enaminone |
| DE19851986.9 | 1998-11-11 | ||
| PCT/EP1999/008366 WO2000027812A1 (de) | 1998-11-11 | 1999-11-02 | Phenyl-substituierte zyklische enaminone |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002529450A JP2002529450A (ja) | 2002-09-10 |
| JP2002529450A5 true JP2002529450A5 (enExample) | 2006-12-14 |
Family
ID=7887420
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000580992A Withdrawn JP2002529450A (ja) | 1998-11-11 | 1999-11-02 | フェニル−置換された環式エナミノン類 |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US6455472B1 (enExample) |
| EP (1) | EP1129071B1 (enExample) |
| JP (1) | JP2002529450A (enExample) |
| KR (1) | KR100646082B1 (enExample) |
| CN (1) | CN1325472C (enExample) |
| AR (1) | AR021150A1 (enExample) |
| AT (1) | ATE307800T1 (enExample) |
| AU (1) | AU770205B2 (enExample) |
| BR (1) | BR9915260A (enExample) |
| CA (1) | CA2350305A1 (enExample) |
| DE (2) | DE19851986A1 (enExample) |
| ES (1) | ES2247838T3 (enExample) |
| HK (1) | HK1042702A1 (enExample) |
| PL (1) | PL348763A1 (enExample) |
| RU (1) | RU2001116103A (enExample) |
| WO (1) | WO2000027812A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19958164A1 (de) * | 1999-12-02 | 2001-06-07 | Bayer Ag | Aryl-substituierte heterozyklische Enaminone |
| DE10021900A1 (de) * | 2000-05-08 | 2001-11-15 | Bayer Ag | Phenyl-substituierte 2-Enamino-Ketonitrile |
| US8076267B2 (en) | 2002-03-01 | 2011-12-13 | W. Neudorff Gmbh Kg | Enhancers for water soluble selective auxin type herbicides |
| US6972273B2 (en) * | 2002-03-01 | 2005-12-06 | W. Neudorff Gmbh Kg | Composition and method for selective herbicide |
| JP2004137270A (ja) * | 2002-09-26 | 2004-05-13 | Nippon Nohyaku Co Ltd | 新規除草剤、その使用方法、新規置換チエノピリミジン誘導体及びその中間体並びにそれらの製造方法 |
| TW200410975A (en) * | 2002-09-26 | 2004-07-01 | Nihon Nohyaku Co Ltd | New pesticide and method for using it, new substituted thienopyrimidine derivative, its intermediate, and method for producing it |
| WO2004096139A2 (en) | 2003-04-24 | 2004-11-11 | Incyte Corporation | Aza spiro alkane derivatives as inhibitors of metalloproteases |
| DE102004049041A1 (de) * | 2004-10-08 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| WO2007143600A2 (en) * | 2006-06-05 | 2007-12-13 | Incyte Corporation | Sheddase inhibitors combined with cd30-binding immunotherapeutics for the treatment of cd30 positive diseases |
| CN102048718A (zh) * | 2009-11-02 | 2011-05-11 | 王泽君 | 烯胺酮类化合物的医疗应用 |
| TW201238487A (en) * | 2011-02-25 | 2012-10-01 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| US8808162B2 (en) | 2011-03-28 | 2014-08-19 | Ams Research Corporation | Implants, tools, and methods for treatment of pelvic conditions |
| US11589583B2 (en) * | 2013-12-03 | 2023-02-28 | Fmc Corporation | Pyrrolidinones herbicides |
| WO2016016131A1 (en) | 2014-07-31 | 2016-02-04 | Syngenta Participations Ag | Pesticidally active cyclic enaminones |
| US10156842B2 (en) | 2015-12-31 | 2018-12-18 | General Electric Company | Device enrollment in a cloud service using an authenticated application |
| CA3017740A1 (en) | 2016-03-16 | 2017-09-21 | Pearlie BURNETTE | Small molecules against cereblon to enhance effector t cell function |
| US11730726B2 (en) | 2018-07-11 | 2023-08-22 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Dimeric immuno-modulatory compounds against cereblon-based mechanisms |
| CN111848450A (zh) * | 2019-04-30 | 2020-10-30 | 帝斯曼知识产权资产管理有限公司 | 一种新的取代的烯胺化合物及其制备方法 |
| JP2025120512A (ja) * | 2022-06-29 | 2025-08-18 | 株式会社Adeka | アゼパンジオン誘導体又はその塩類及び該化合物を含有する有害生物防除剤並びにその使用方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2920183A1 (de) * | 1979-05-17 | 1981-04-30 | Schering Ag Berlin Und Bergkamen, 1000 Berlin | Thiazolyliden-oxo-propionitrile, insektizide mittel enthaltend diese verbindungen sowie verfahren zu ihrer herstellung |
| DE3529259A1 (de) * | 1985-08-16 | 1987-02-26 | Bayer Ag | Verfahren zur herstellung von halogensubstituierten benzoylacetonitrilen, 1-chlor-2-(2,4-dichlor-5-fluorphenyl)-ethan-2-on und seine herstellung |
| US5747424A (en) * | 1989-09-11 | 1998-05-05 | Rhone-Poulenc Agriculture Ltd. | Herbicidal 4-substituted isoxazol |
| GB8928524D0 (en) * | 1989-12-18 | 1990-02-21 | Shell Int Research | Herbicidal acrylonitrile derivatives |
| DE4040021A1 (de) * | 1990-12-14 | 1992-06-17 | Bayer Ag | Substituierte 2,2-difluor-1,3-benzodioxyl-4-ketone |
| US5804532A (en) * | 1991-01-25 | 1998-09-08 | Rhone-Poulenc Agriculture Limited | Herbicidal 2-cyano-1,3-diones |
| FR2682379B1 (fr) * | 1991-10-09 | 1994-02-11 | Rhone Poulenc Agrochimie | Nouveaux phenylpyrazoles fongicides. |
-
1998
- 1998-11-11 DE DE19851986A patent/DE19851986A1/de not_active Withdrawn
-
1999
- 1999-11-02 BR BR9915260-6A patent/BR9915260A/pt not_active IP Right Cessation
- 1999-11-02 CA CA002350305A patent/CA2350305A1/en not_active Abandoned
- 1999-11-02 DE DE59912719T patent/DE59912719D1/de not_active Expired - Fee Related
- 1999-11-02 KR KR1020017004969A patent/KR100646082B1/ko not_active Expired - Fee Related
- 1999-11-02 PL PL99348763A patent/PL348763A1/xx not_active Application Discontinuation
- 1999-11-02 ES ES99955944T patent/ES2247838T3/es not_active Expired - Lifetime
- 1999-11-02 WO PCT/EP1999/008366 patent/WO2000027812A1/de not_active Ceased
- 1999-11-02 JP JP2000580992A patent/JP2002529450A/ja not_active Withdrawn
- 1999-11-02 AT AT99955944T patent/ATE307800T1/de not_active IP Right Cessation
- 1999-11-02 CN CNB99813208XA patent/CN1325472C/zh not_active Expired - Fee Related
- 1999-11-02 AU AU12688/00A patent/AU770205B2/en not_active Ceased
- 1999-11-02 HK HK02104242.6A patent/HK1042702A1/zh unknown
- 1999-11-02 RU RU2001116103/04A patent/RU2001116103A/ru not_active Application Discontinuation
- 1999-11-02 US US09/831,261 patent/US6455472B1/en not_active Expired - Fee Related
- 1999-11-02 EP EP99955944A patent/EP1129071B1/de not_active Expired - Lifetime
- 1999-11-11 AR ARP990105739A patent/AR021150A1/es not_active Application Discontinuation
-
2002
- 2002-07-26 US US10/206,426 patent/US20030130125A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002529450A5 (enExample) | ||
| JP2004538327A5 (enExample) | ||
| JP2003506352A5 (enExample) | ||
| JP2005522484A5 (enExample) | ||
| JP2007526271A5 (enExample) | ||
| JP2005503419A5 (enExample) | ||
| JP2002518389A5 (enExample) | ||
| EP0377893A3 (de) | 3-Aryl-pyrrolidin-2,4-dion-Derivate | |
| HU9302651D0 (en) | Fungicides containing carboxylic acid anilides and process for producing active ingredients thereof | |
| RU2008135317A (ru) | Фунгицидные -циклоалкилбензиламидные производные | |
| ATE106392T1 (de) | Arylpyrrole als insektizide, acarizide und nematizide mittel und verfahren zu ihrer herstellung. | |
| JP2005502658A5 (enExample) | ||
| HUT67924A (en) | Fungicidal compositions containing 2-(substituted phenyl)-3-methoxy-propenecarboxylates as active ingredients, process for producing the active ingredients, and method for combatting fungi | |
| EP0055105A3 (en) | Triazolinones, and their production and use | |
| MA32749B1 (fr) | Composes insecticides | |
| KR940014307A (ko) | N-아세토닐벤즈아미드 화합물들 및 살균제로서의 그 용법 | |
| RU2018103198A (ru) | Новые соединения циклического n-карбоксамида, применяемые в качестве гербицидов | |
| WO2002048146A3 (de) | Verwendung von substituierten imidazoazinen, neue imidazoazine, verfahren zu deren herstellung, sowie sie enthaltende mittel | |
| JP2004501144A5 (enExample) | ||
| JP2003529613A5 (enExample) | ||
| RU2007113188A (ru) | Замещенные изоксазолы в качестве фунгицидов | |
| BR9915534A (pt) | 1-piridil substituìdo)-1,2,4-triazóis inseticidas | |
| JPH09110611A5 (enExample) | ||
| KR950703504A (ko) | 살충성 플루오로올레핀(pesticidal fluoroolefins) | |
| JP2004524299A5 (enExample) |