JP2004503552A5 - - Google Patents
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- JP2004503552A5 JP2004503552A5 JP2002510475A JP2002510475A JP2004503552A5 JP 2004503552 A5 JP2004503552 A5 JP 2004503552A5 JP 2002510475 A JP2002510475 A JP 2002510475A JP 2002510475 A JP2002510475 A JP 2002510475A JP 2004503552 A5 JP2004503552 A5 JP 2004503552A5
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- 150000001875 compounds Chemical class 0.000 description 12
- 239000003085 diluting agent Substances 0.000 description 11
- 125000000217 alkyl group Chemical group 0.000 description 10
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 150000002431 hydrogen Chemical class 0.000 description 6
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical group 0.000 description 5
- 125000005842 heteroatom Chemical group 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 0 CC(C(*1O)=O)=C(*)C1(C(F)(F)F)P Chemical compound CC(C(*1O)=O)=C(*)C1(C(F)(F)F)P 0.000 description 3
- 125000006350 alkyl thio alkyl group Chemical group 0.000 description 3
- 125000001072 heteroaryl group Chemical group 0.000 description 3
- -1 polyalkoxyalkyl Chemical group 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- 150000001266 acyl halides Chemical class 0.000 description 1
- 125000005108 alkenylthio group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- NBYQXBYMEUOBON-UHFFFAOYSA-N carbamothioyl chloride Chemical compound NC(Cl)=S NBYQXBYMEUOBON-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- LRYSUGTXBIPBGB-UHFFFAOYSA-N chloromethanedithioic acid Chemical compound SC(Cl)=S LRYSUGTXBIPBGB-UHFFFAOYSA-N 0.000 description 1
- KTRFZWJCHOQHMN-UHFFFAOYSA-N chloromethanethioic s-acid Chemical compound SC(Cl)=O KTRFZWJCHOQHMN-UHFFFAOYSA-N 0.000 description 1
- 125000005366 cycloalkylthio group Chemical group 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002540 isothiocyanates Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 description 1
- 125000003884 phenylalkyl 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
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10029077A DE10029077A1 (de) | 2000-06-13 | 2000-06-13 | Thiazolylsubstituierte Heterocyclen |
| DE10029077.9 | 2000-06-13 | ||
| PCT/EP2001/006174 WO2001096333A1 (de) | 2000-06-13 | 2001-05-31 | Hetarylsubstituierte heterocyclen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004503552A JP2004503552A (ja) | 2004-02-05 |
| JP2004503552A5 true JP2004503552A5 (cg-RX-API-DMAC7.html) | 2008-07-17 |
| JP5156164B2 JP5156164B2 (ja) | 2013-03-06 |
Family
ID=7645557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002510475A Expired - Fee Related JP5156164B2 (ja) | 2000-06-13 | 2001-05-31 | ヘタリール−置換複素環式化合物 |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US6767864B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1296979B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5156164B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR100820600B1 (cg-RX-API-DMAC7.html) |
| CN (2) | CN1230435C (cg-RX-API-DMAC7.html) |
| AR (1) | AR028698A1 (cg-RX-API-DMAC7.html) |
| AT (1) | ATE315037T1 (cg-RX-API-DMAC7.html) |
| AU (2) | AU2001276354B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR0111625A (cg-RX-API-DMAC7.html) |
| CA (1) | CA2411111C (cg-RX-API-DMAC7.html) |
| DE (2) | DE10029077A1 (cg-RX-API-DMAC7.html) |
| DK (1) | DK1296979T3 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2254453T3 (cg-RX-API-DMAC7.html) |
| MX (1) | MXPA02012400A (cg-RX-API-DMAC7.html) |
| TW (1) | TWI290142B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2001096333A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10331675A1 (de) * | 2003-07-14 | 2005-02-10 | Bayer Cropscience Ag | Hetarylsubstituierte Pyrazolidindion-Derivate |
| JP4568361B2 (ja) * | 2005-04-22 | 2010-10-27 | アラントス・ファーマシューティカルズ・ホールディング・インコーポレーテッド | ジペプチジルペプチダーゼ−ｉｖ阻害剤 |
| GB0712653D0 (en) | 2007-06-28 | 2007-08-08 | Syngenta Ltd | Novel herbicides |
| GB0717082D0 (en) * | 2007-09-03 | 2007-10-10 | Syngenta Ltd | Novel herbicides |
| GB0812310D0 (en) * | 2008-07-03 | 2008-08-13 | Syngenta Ltd | Novel herbicides |
| KR101925162B1 (ko) | 2011-03-11 | 2018-12-04 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 시스-알콕시-치환된 스피로시클릭 1-h-피롤리딘-2,4-디온 유도체 |
| WO2013021044A1 (de) | 2011-08-11 | 2013-02-14 | Bayer Intellectual Property Gmbh | 1,2,4-triazolyl-substituierte ketoenole |
| US9353072B2 (en) * | 2012-10-31 | 2016-05-31 | Purdue Research Foundation | Antimicrobial substituted thiazoles and methods of use |
| EP3658551B1 (en) * | 2017-07-24 | 2022-01-19 | Redag Crop Protection Ltd | Benzoxazinone derivatives useful as herbicides |
| CN114149433A (zh) * | 2020-09-07 | 2022-03-08 | 海利尔药业集团股份有限公司 | 一种含氮螺环衍生物或其作为农药可接受的盐、组合物及其用途 |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1139940A (en) * | 1913-01-03 | 1915-05-18 | Myrtle Desk Company | Locking device for desks and the like. |
| NL130759C (cg-RX-API-DMAC7.html) | 1965-10-07 | |||
| EP0000539A1 (en) * | 1977-07-27 | 1979-02-07 | Ciba-Geigy Ag | Copper complexes of N-pyrazole, N-imidazole and N-triazole acetanilides, their preparation and their use as fungicides |
| MA18800A1 (fr) * | 1979-04-10 | 1980-12-31 | Ciba Geigy Ag | Naphtylamines acylees,procede pour leur preparation et leur application comme phytofongicides |
| DE2915026A1 (de) * | 1979-04-12 | 1980-10-30 | Bayer Ag | N,n-disubstituierte ethylglycin (thiol)ester, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
| US4296237A (en) | 1979-09-11 | 1981-10-20 | Merck & Co., Inc. | 4-(Pyridyl, piperazinyl and thiazolyl substituted thiazolyl)-3-hydroxy-3-pyrroline-2,5-diones |
| US4298743A (en) | 1979-09-11 | 1981-11-03 | Merck & Co., Inc. | 4-(Substituted phenyl thiazolyl)-3-hydroxy-3-pyrroline-2,5-diones |
| US4379791A (en) * | 1979-09-11 | 1983-04-12 | Merck & Co., Inc. | 4-(Substituted thiazolyl)-3-hydroxy-3-pyrroline-2,5-dione inhibitors of glycolic acid oxidase |
| US4377588A (en) * | 1979-09-11 | 1983-03-22 | Merck Sharp & Dohme (I.A.) Corp. | 4-(Substituted thiazolyl)-3-hydroxy-3-pyrroline-2,5-dione inhibitors of glycolic acid oxidase |
| DE3126083A1 (de) * | 1981-07-02 | 1983-01-20 | Basf Ag, 6700 Ludwigshafen | N-substituierte 2-methylnaphthylamide, verfahren zu ihrer herstellung und diese enthaltende fungizide |
| CN1003445B (zh) | 1984-10-03 | 1989-03-01 | 武田药品工业株式会社 | 噻唑烷二酮衍生物，其制备方法和用途 |
| GB8531608D0 (en) | 1985-12-23 | 1986-02-05 | Beecham Group Plc | Treatment |
| WO1989008652A1 (en) | 1988-03-08 | 1989-09-21 | Pfizer Inc. | Thiazolidinedione derivatives as hypoglycemic agents |
| DE3811120A1 (de) * | 1988-03-31 | 1989-10-12 | Merckle Gmbh | Neopentylesterderivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| GB8826035D0 (en) * | 1988-11-07 | 1988-12-14 | Ici Plc | Herbicidal compositions |
| DE3841732A1 (de) * | 1988-12-10 | 1990-06-13 | Hoechst Ag | Dipeptid-derivate mit enzym-inhibitorischer wirkung |
| ES2081863T3 (es) * | 1989-03-22 | 1996-03-16 | Ciba Geigy Ag | Plaguicidas. |
| EP0516069B1 (en) * | 1991-05-31 | 1996-04-24 | Sumitomo Pharmaceuticals Company, Limited | Leukotriene B4 antagonist |
| CA2075154A1 (en) * | 1991-08-06 | 1993-02-07 | Neelakantan Balasubramanian | Peptide aldehydes as antithrombotic agents |
| JP3232350B2 (ja) * | 1992-03-25 | 2001-11-26 | 武田薬品工業株式会社 | 縮環したチアジアゾール誘導体、その製造法および用途 |
| US5728720A (en) | 1993-12-27 | 1998-03-17 | Japan Tobacco Inc. | Isoxazolidinedione compounds and use thereof |
| EP0792272A1 (de) * | 1994-11-17 | 1997-09-03 | Bayer Ag | Substituierte thiophenderivate als schädlingsbekämpfungsmittel und herbizide |
| IL118325A0 (en) * | 1995-05-25 | 1996-10-31 | Pont Merck And Pharmaceutical | Integrin receptor antagonists and pharmaceutical compositions containing them |
| US5674242A (en) * | 1995-06-06 | 1997-10-07 | Quanam Medical Corporation | Endoprosthetic device with therapeutic compound |
| BR9708425B1 (pt) * | 1996-04-02 | 2012-02-22 | fenilcetoenóis substituìdos, processo para preparação e uso dos mesmos, bem como pesticidas ou herbicidas e método para controle de pragas e ervas daninhas. | |
| CN1156470C (zh) * | 1996-05-10 | 2004-07-07 | 拜尔公司 | 新的取代的吡啶基酮烯醇 |
| AR011164A1 (es) * | 1997-02-28 | 2000-08-02 | Lilly Co Eli | Compuestos heterociclicos, composiciones farmaceuticas que los comprenden, y metodos para inhibir la liberacion del peptido beta-amiloide y/o su sintesismediante el uso de dichos compuestos |
| AR012443A1 (es) * | 1997-04-16 | 2000-10-18 | Uriach & Cia Sa J | Nuevas carboxamidas como inhibidores de la agregacion plaquetaria, procedimiento para su preparacion, composiciones farmaceuticas que loscontienen y uso de los mismos en la manufactura de medicamentos |
| US6514977B1 (en) * | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
| GB9726989D0 (en) * | 1997-12-22 | 1998-02-18 | Ciba Geigy Ag | Organic compounds |
| JP3538107B2 (ja) * | 2000-03-14 | 2004-06-14 | 日本碍子株式会社 | 放射性廃棄物の投入容器カバー及びこれを用いた放射性廃棄物の投入方法 |
| DE10152005A1 (de) * | 2001-10-22 | 2003-04-30 | Bayer Cropscience Ag | Pyrazolylsubstituierte Heterocyclen |
-
2000
- 2000-06-13 DE DE10029077A patent/DE10029077A1/de not_active Withdrawn
-
2001
- 2001-05-31 CN CNB018111475A patent/CN1230435C/zh not_active Expired - Fee Related
- 2001-05-31 BR BR0111625-8A patent/BR0111625A/pt not_active IP Right Cessation
- 2001-05-31 MX MXPA02012400A patent/MXPA02012400A/es active IP Right Grant
- 2001-05-31 AT AT01953967T patent/ATE315037T1/de not_active IP Right Cessation
- 2001-05-31 EP EP01953967A patent/EP1296979B1/de not_active Expired - Lifetime
- 2001-05-31 JP JP2002510475A patent/JP5156164B2/ja not_active Expired - Fee Related
- 2001-05-31 ES ES01953967T patent/ES2254453T3/es not_active Expired - Lifetime
- 2001-05-31 CN CNB2005100754029A patent/CN100363361C/zh not_active Expired - Fee Related
- 2001-05-31 WO PCT/EP2001/006174 patent/WO2001096333A1/de not_active Ceased
- 2001-05-31 DK DK01953967T patent/DK1296979T3/da active
- 2001-05-31 AU AU2001276354A patent/AU2001276354B2/en not_active Ceased
- 2001-05-31 CA CA2411111A patent/CA2411111C/en not_active Expired - Fee Related
- 2001-05-31 AU AU7635401A patent/AU7635401A/xx active Pending
- 2001-05-31 KR KR1020027015595A patent/KR100820600B1/ko not_active Expired - Fee Related
- 2001-05-31 US US10/297,873 patent/US6767864B2/en not_active Expired - Lifetime
- 2001-05-31 DE DE50108624T patent/DE50108624D1/de not_active Expired - Lifetime
- 2001-06-08 TW TW090113900A patent/TWI290142B/zh active
- 2001-06-11 AR ARP010102756A patent/AR028698A1/es active IP Right Grant
-
2004
- 2004-05-21 US US10/850,679 patent/US7141533B2/en not_active Expired - Fee Related
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