JP2015535834A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015535834A5 JP2015535834A5 JP2015533561A JP2015533561A JP2015535834A5 JP 2015535834 A5 JP2015535834 A5 JP 2015535834A5 JP 2015533561 A JP2015533561 A JP 2015533561A JP 2015533561 A JP2015533561 A JP 2015533561A JP 2015535834 A5 JP2015535834 A5 JP 2015535834A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- alkyl
- different
- alkylsilyl
- 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
- -1 substituted Chemical class 0.000 claims 67
- 125000000623 heterocyclic group Chemical group 0.000 claims 41
- 125000005103 alkyl silyl group Chemical group 0.000 claims 27
- 229910052736 halogen Inorganic materials 0.000 claims 27
- 150000002367 halogens Chemical class 0.000 claims 27
- 229910052739 hydrogen Inorganic materials 0.000 claims 27
- 239000001257 hydrogen Substances 0.000 claims 26
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 23
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 16
- 125000005842 heteroatom Chemical group 0.000 claims 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 15
- 229910052799 carbon Inorganic materials 0.000 claims 15
- 125000004432 carbon atom Chemical group C* 0.000 claims 15
- 125000003118 aryl group Chemical group 0.000 claims 14
- NHFDIUPJVYYTLG-UHFFFAOYSA-N carbononitridic isocyanide Chemical compound [C-]#[N+]C#N NHFDIUPJVYYTLG-UHFFFAOYSA-N 0.000 claims 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 12
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims 11
- 150000002431 hydrogen Chemical class 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 7
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 6
- 125000001769 aryl amino group Chemical group 0.000 claims 6
- 125000005163 aryl sulfanyl group Chemical group 0.000 claims 6
- 125000004104 aryloxy group Chemical group 0.000 claims 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 6
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 6
- 125000001475 halogen functional group Chemical group 0.000 claims 6
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 6
- 241001481833 Coryphaena hippurus Species 0.000 claims 5
- 241000233866 Fungi Species 0.000 claims 5
- 125000005018 aryl alkenyl group Chemical group 0.000 claims 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 5
- 125000005292 haloalkynyloxy group Chemical group 0.000 claims 5
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 5
- 244000005700 microbiome Species 0.000 claims 5
- 230000003032 phytopathogenic effect Effects 0.000 claims 5
- 125000005122 aminoalkylamino group Chemical group 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- 125000004434 sulfur atom Chemical group 0.000 claims 3
- FNJPMIYMKZBZCC-UHFFFAOYSA-N 4,5-dihydro-1,2-oxazole quinoline Chemical class C1CC=NO1.N1=CC=CC2=CC=CC=C21 FNJPMIYMKZBZCC-UHFFFAOYSA-N 0.000 claims 2
- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims 2
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 125000005647 linker group Chemical group 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 230000009261 transgenic effect Effects 0.000 claims 2
- XMCAJYZIJTWANG-HUQDXCLPSA-N (1R,2R)-4-(dimethylamino)-1-[6-[(E)-hydroxyiminomethyl]-2-methoxyquinolin-3-yl]-2-naphthalen-1-yl-1-phenylbutan-2-ol Chemical compound CN(CC[C@]([C@H](C1=CC=CC=C1)C=1C(=NC2=CC=C(C=C2C1)/C=N/O)OC)(O)C1=CC=CC2=CC=CC=C12)C XMCAJYZIJTWANG-HUQDXCLPSA-N 0.000 claims 1
- MRFPRJAZMYOHJW-MKCMJLOXSA-N (1R,2R)-6-(dimethylamino)-1-[6-[(E)-hydroxyiminomethyl]-2-methoxyquinolin-3-yl]-2-naphthalen-2-yl-1-phenylhexan-2-ol Chemical compound CN(CCCC[C@]([C@H](C1=CC=CC=C1)C=1C(=NC2=CC=C(C=C2C1)/C=N/O)OC)(O)C1=CC2=CC=CC=C2C=C1)C MRFPRJAZMYOHJW-MKCMJLOXSA-N 0.000 claims 1
- XMCAJYZIJTWANG-BABVVNGDSA-N (1R,2S)-4-(dimethylamino)-1-[6-[(E)-hydroxyiminomethyl]-2-methoxyquinolin-3-yl]-2-naphthalen-1-yl-1-phenylbutan-2-ol Chemical compound CN(CC[C@@]([C@H](C1=CC=CC=C1)C=1C(=NC2=CC=C(C=C2C1)/C=N/O)OC)(O)C1=CC=CC2=CC=CC=C12)C XMCAJYZIJTWANG-BABVVNGDSA-N 0.000 claims 1
- MRFPRJAZMYOHJW-YHJIWIJTSA-N (1R,2S)-6-(dimethylamino)-1-[6-[(E)-hydroxyiminomethyl]-2-methoxyquinolin-3-yl]-2-naphthalen-2-yl-1-phenylhexan-2-ol Chemical compound CN(CCCC[C@@]([C@H](C1=CC=CC=C1)C=1C(=NC2=CC=C(C=C2C1)/C=N/O)OC)(O)C1=CC2=CC=CC=C2C=C1)C MRFPRJAZMYOHJW-YHJIWIJTSA-N 0.000 claims 1
- SBEPSOQMHPACTJ-HPMWZEIGSA-N (5R,6S)-6-[(1R)-1-hydroxyethyl]-3-[2-[(E)-hydroxyiminomethyl]phenanthridin-8-yl]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid Chemical compound O[C@H](C)[C@@H]1[C@H]2CC(=C(N2C1=O)C(=O)O)C1=CC2=CN=C3C=CC(=CC3=C2C=C1)/C=N/O SBEPSOQMHPACTJ-HPMWZEIGSA-N 0.000 claims 1
- DWAZFYIKSQOJPD-WUXMJOGZSA-N (NE)-N-[(5-nitroquinolin-6-yl)methylidene]hydroxylamine Chemical compound [O-][N+](=O)c1c(/C=N/O)ccc2ncccc21 DWAZFYIKSQOJPD-WUXMJOGZSA-N 0.000 claims 1
- DWAZFYIKSQOJPD-SDQBBNPISA-N (NZ)-N-[(5-nitroquinolin-6-yl)methylidene]hydroxylamine Chemical compound [O-][N+](=O)c1c(\C=N/O)ccc2ncccc21 DWAZFYIKSQOJPD-SDQBBNPISA-N 0.000 claims 1
- OPQQWAGBFJQALJ-KPKJPENVSA-N (ne)-n-(quinolin-6-ylmethylidene)hydroxylamine Chemical compound N1=CC=CC2=CC(/C=N/O)=CC=C21 OPQQWAGBFJQALJ-KPKJPENVSA-N 0.000 claims 1
- LIORMTVHNLXADF-AWNIVKPZSA-N (ne)-n-[(5-aminoquinolin-6-yl)methylidene]hydroxylamine Chemical compound C1=CC=C2C(N)=C(\C=N\O)C=CC2=N1 LIORMTVHNLXADF-AWNIVKPZSA-N 0.000 claims 1
- QEPYTBPNSWTPJK-UHFFFAOYSA-N 4,5-dihydro-1,2-oxazole-5-carbothioic S-acid quinoline Chemical compound SC(=O)C1CC=NO1.c1ccc2ncccc2c1 QEPYTBPNSWTPJK-UHFFFAOYSA-N 0.000 claims 1
- LDTYZQPHTJSMGY-UHFFFAOYSA-N 4,5-dihydro-1,2-oxazole-5-carboxylic acid quinoline Chemical compound O1N=CCC1C(=O)O.N1=CC=CC2=CC=CC=C12 LDTYZQPHTJSMGY-UHFFFAOYSA-N 0.000 claims 1
- 239000004606 Fillers/Extenders Substances 0.000 claims 1
- DIMCRNMCHZWYNQ-UHFFFAOYSA-N N-hydroxyquinoline-6-carboximidoyl chloride Chemical compound ON=C(Cl)c1ccc2ncccc2c1 DIMCRNMCHZWYNQ-UHFFFAOYSA-N 0.000 claims 1
- TYEZCLFGKKCDTG-UHFFFAOYSA-N N-hydroxyquinoline-6-carboximidoyl chloride hydrochloride Chemical compound Cl.ON=C(Cl)c1ccc2ncccc2c1 TYEZCLFGKKCDTG-UHFFFAOYSA-N 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- XDZGUHUIWVRDMX-HVYLCQPDSA-N [Na].O[C@H](C)[C@@H]1[C@H]2CC(=C(N2C1=O)C(=O)O)C1=CC2=CN=C3C=CC(=CC3=C2C=C1)/C=N/O Chemical compound [Na].O[C@H](C)[C@@H]1[C@H]2CC(=C(N2C1=O)C(=O)O)C1=CC2=CN=C3C=CC(=CC3=C2C=C1)/C=N/O XDZGUHUIWVRDMX-HVYLCQPDSA-N 0.000 claims 1
- 230000000895 acaricidal effect Effects 0.000 claims 1
- 239000000642 acaricide Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 230000000844 anti-bacterial effect Effects 0.000 claims 1
- 239000005667 attractant Substances 0.000 claims 1
- 239000003899 bactericide agent Substances 0.000 claims 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000002871 fertility agent Substances 0.000 claims 1
- 239000003337 fertilizer Substances 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 150000002527 isonitriles Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000005645 nematicide Substances 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000004548 quinolin-3-yl group Chemical group N1=CC(=CC2=CC=CC=C12)* 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 0 CC1(*)C(c2c(*)c(*)c3nc(*)c(*)c(*)c3c2*)=NOC1(C)C(N(*)**)=* Chemical compound CC1(*)C(c2c(*)c(*)c3nc(*)c(*)c(*)c3c2*)=NOC1(C)C(N(*)**)=* 0.000 description 5
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12186485 | 2012-09-28 | ||
| EP12186485.4 | 2012-09-28 | ||
| PCT/EP2013/069893 WO2014048940A2 (en) | 2012-09-28 | 2013-09-25 | Nitrogen-containing heterocyclic compounds for plant disease control |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015535834A JP2015535834A (ja) | 2015-12-17 |
| JP2015535834A5 true JP2015535834A5 (enExample) | 2016-06-23 |
| JP6118907B2 JP6118907B2 (ja) | 2017-04-19 |
Family
ID=47048991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015533561A Active JP6118907B2 (ja) | 2012-09-28 | 2013-09-25 | 植物病害を防除するための窒素含有ヘテロ環式化合物 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US9510598B2 (enExample) |
| EP (1) | EP2900661B1 (enExample) |
| JP (1) | JP6118907B2 (enExample) |
| CN (1) | CN104812751B (enExample) |
| AR (1) | AR092727A1 (enExample) |
| BR (1) | BR112015007159A2 (enExample) |
| TW (1) | TWI579281B (enExample) |
| WO (1) | WO2014048940A2 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5976837B2 (ja) * | 2011-12-29 | 2016-08-24 | 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 | 殺菌性３−［（１，３−チアゾール−４−イルメトキシイミノ）（フェニル）メチル］−２−置換−１，２，４−オキサジアゾール−５（２ｈ）−オン誘導体 |
| JP2017095353A (ja) * | 2014-03-27 | 2017-06-01 | 日本曹達株式会社 | イソオキサゾリン−５−カルボキサミド化合物および有害生物防除剤 |
| CN105753853B (zh) | 2014-12-16 | 2020-08-04 | 沈阳中化农药化工研发有限公司 | 一种含异恶唑啉的脲嘧啶类化合物及其用途 |
| HUE056695T2 (hu) | 2017-06-13 | 2022-03-28 | Bayer Ag | Tetrahidro- és dihidrofurán-karbonsav-amidok gyomirtó 3-fenilizoxazolin-5-karboxamidjai |
| EP3638665B1 (de) | 2017-06-13 | 2021-07-21 | Bayer Aktiengesellschaft | Herbizid wirksame 3-phenylisoxazolin-5-carboxamide von tetrahydro- und dihydrofurancarbonsäuren und -estern |
| US20200369630A1 (en) | 2017-08-17 | 2020-11-26 | Bayer Aktiengesellschaft | Herbicidally active 3-phenyl-5-trifluoromethylisoxazoline-5-carboxamides of cyclopentylcarboxylic acids and esters |
| JP7217751B2 (ja) | 2018-01-25 | 2023-02-03 | バイエル・アクチエンゲゼルシヤフト | 除草活性を示すシクロペンテニルカルボン酸誘導体の３－フェニルイソオキサゾリン－５－カルボキサミド類 |
| CN108913698B (zh) * | 2018-07-25 | 2021-10-26 | 安徽农业大学 | 一种与小麦穗发芽抗性/感性相关的caps标记及其应用 |
| CA3133025A1 (en) | 2019-03-12 | 2020-09-17 | Bayer Aktiengesellschaft | Herbicidally active 3-phenylisoxazoline-5-carboxamides of s-containing cyclopentenyl carboxylic acid esters |
| ES2980695T3 (es) * | 2019-04-19 | 2024-10-02 | Lg Chemical Ltd | Profármaco de inhibidor de caspasas |
| CN113891704A (zh) * | 2019-05-31 | 2022-01-04 | 株式会社Lg化学 | 半胱天冬酶抑制剂前药注射用组合物 |
| US12617803B2 (en) * | 2020-05-05 | 2026-05-05 | Basf Se | Condensed isoxazoline derivatives and their use as herbicides |
| JP7844432B2 (ja) | 2020-07-23 | 2026-04-13 | バイエル アクチェンゲゼルシャフト | アミノフランの調製方法 |
| WO2022128746A1 (en) | 2020-12-14 | 2022-06-23 | Elanco Tiergesundheit Ag | Quinoline derivatives as endoparasiticides |
| KR102636905B1 (ko) | 2021-09-15 | 2024-02-15 | 한국화학연구원 | 살균제로서의 7번 위치가 치환된 5-니트로 퀴놀린 화합물 |
| CN120794925A (zh) * | 2024-04-10 | 2025-10-17 | 青岛清原化合物有限公司 | 3-苯基异噁唑啉-5-甲酰胺类化合物及其制备方法、除草组合物和应用 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1369233A (en) * | 1971-04-15 | 1974-10-02 | Science Union & Cie | Thiohydroxamic acid derivatives and processes for preparing them |
| UA78548C2 (en) * | 2002-03-29 | 2007-04-10 | Janssen Pharmaceutica Nv | Radiolabelled quinoline and quinolinone derivatives and use thereof as metabotropic ligands of glutamate receptor |
| WO2006090234A1 (en) * | 2005-02-22 | 2006-08-31 | Ranbaxy Laboratories Limited | Heterocyclic derivatives as cell adhesion inhibitors |
| KR100774999B1 (ko) * | 2005-02-26 | 2007-11-09 | 주식회사 엘지생명과학 | 이소옥사졸린 유도체 및 그의 제조 방법 |
| MX2009004786A (es) * | 2006-10-31 | 2009-06-05 | Schering Corp | Derivados de anilinopiperazina y sus metodos de uso. |
| JP2009286773A (ja) * | 2008-03-14 | 2009-12-10 | Bayer Cropscience Ag | 殺虫性縮環式アリール類 |
| EP2394995B1 (en) * | 2009-02-03 | 2014-01-15 | Kumiai Chemical Industry CO., LTD. | Ring-fused 2-pyridone derivatives and herbicides |
| JP2011098956A (ja) * | 2009-10-09 | 2011-05-19 | Sumitomo Chemical Co Ltd | イソオキサゾリン化合物及びその用途 |
-
2013
- 2013-09-25 WO PCT/EP2013/069893 patent/WO2014048940A2/en not_active Ceased
- 2013-09-25 BR BR112015007159A patent/BR112015007159A2/pt active Search and Examination
- 2013-09-25 JP JP2015533561A patent/JP6118907B2/ja active Active
- 2013-09-25 CN CN201380061985.2A patent/CN104812751B/zh not_active Expired - Fee Related
- 2013-09-25 US US14/430,919 patent/US9510598B2/en not_active Expired - Fee Related
- 2013-09-25 EP EP13766959.4A patent/EP2900661B1/en not_active Not-in-force
- 2013-09-27 AR ARP130103500A patent/AR092727A1/es unknown
- 2013-09-27 TW TW102134912A patent/TWI579281B/zh not_active IP Right Cessation
-
2016
- 2016-10-27 US US15/335,832 patent/US9776993B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5608676B2 (ja) | イソオキサゾリン誘導体及びその殺虫剤としての使用 | |
| JP2018502912A5 (enExample) | ||
| WO2006078621A3 (en) | 2-phenoxy-n- (1, 3 , 4-thiadizol-2-yl) pyridin-3-amine derivatives and related compounds as p2y1 receptor inhibitors for the treatment of thromboembolic disorders | |
| EA200500304A1 (ru) | Производные 3-(сульфонамидоэтил)индола, предназначенные для использования в качестве миметиков глюкокортикоидов при лечении воспалительных, аллергических и пролиферативных заболеваний | |
| JP2018509417A5 (enExample) | ||
| JP2017538785A5 (enExample) | ||
| JP2018509418A5 (enExample) | ||
| RU2010107171A (ru) | Фунгицидные n-циклоалкилбензилтиокарбоксамиды или n-циклоалкилбензил-n, -замещенные амидиновые производные | |
| JP2019514956A5 (enExample) | ||
| JP2013501720A5 (enExample) | ||
| JP2006524222A5 (enExample) | ||
| JP2007513901A5 (enExample) | ||
| JP2007537172A5 (enExample) | ||
| JP2017537882A5 (enExample) | ||
| WO2007125405A3 (en) | Substituted 2-amino-fused heterocyclic compounds | |
| JP2010534716A5 (enExample) | ||
| JP2009532437A5 (enExample) | ||
| JP2016504378A5 (enExample) | ||
| AR045389A1 (es) | Inhibidores del c-kit con estructura de pirazolil-amidil-benzoimidazolilo n-sustituido | |
| UA98652C2 (uk) | Похідна n-циклоалкілкарбоксаміду, фунгіцидна композиція та спосіб боротьби із фітопатогенними грибами сільськогосподарських культур | |
| WO2009016218A3 (en) | Fungicide n-cycloalkyl-n-bicyclic-carboxamide derivatives | |
| JP2017511378A5 (enExample) | ||
| JP2018505876A5 (enExample) | ||
| JP2005516037A5 (enExample) | ||
| JP2006511446A5 (enExample) |