http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0419944-A2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-34 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-74 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-34 |
| filingDate | 1990-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0db24d3aaa0435e342930be41dd8b312 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a591e9071fc250112279fbce8278881 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8605dfcc48c8e6a4baa462a55b30582 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_989440272453cfaf28ed82a8e40563b9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4933440f37aeb97f5cc2937cb1a872cc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_185741e5f2b496ee0478b652ad61e849 |
| publicationDate | 1991-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0419944-A2 |
| titleOfInvention | Oxazole and thiazole carboxylic acid amines |
| abstract | X Sauerstoff oder Schwefel; R 1 Wasserstoff; Halogen; gegebenenfalls substituiertes C 1 -C 6 -Alkyl, Benzyl, Cycloalkyl, Alkenyl, Alkinyl, Phenyl, Phenoxy oder Phenylthio; Alkoxy; Alkylthio; Halogenalkoxy; Halogenalkylthio; oder einen gegebenenfalls substituierten 5- bis 6-gliedrigen heterocyclischen Rest; R 2 Formyl, 4,5-Dihydrooxazol-2-yl oder den Rest -COYR 5 ; Y Sauerstoff oder Schwefel; R 5 Wasserstoff; Cycloalkyl; gegebenenfalls substituiertes Alkyl, Phenyl, Benzyl, Alkenyl, Cycloalkenyl oder Alkinyl; einen gegebenenfalls substituierten 5- oder 6-gliedrigen heterocyclischen Rest; Phthalimido; Tetrahydrophthalimido; Succinimido; Maleinimido; ein Äquivalent eines Kations; oder einen Rest -N = CR 6 R 7 ; R 6 , R 7 Wasserstoff; Alkyl; Cycloalkyl; Phenyl; Furyl oder zusammen eine Methylenkette mit 4 bis 7 Kettengliedern; R 3 Wasserstoff oder gegebenenfalls substituiertes Alkyl oder Cycloalkyl; R 4 Hydroxy; Alkoxy; gegebenenfalls substituiertes Alkyl, Cycloalkyl, Alkenyl, Alkinyl, Phenyl oder Naphthyl; einen gegebenenfalls substituierten 5- bis 6-gliedrigen heterocyclischen Rest; oder R 3 und R 4 gemeinsam einen Rest der Struktur -(CH 2 ) n -Y P -(CH 2 ) q -, wobei n und q 1, 2 oder 3, p 0 oder 1 und Y Sauerstoff, Schwefel oder N-Methyl bedeuten oder den Rest der Formel -(CH 2 ) 3 -CO- bilden, sowie deren umweltverträgliche Salze, nwobei in der Formel Ib X nicht Schwefel bedeutet, wenn R 1 3-Pyridyl, R 2 C0 2 CH 2 CH 3 oder R 3 Wasserstoff bedeutet, und wobei in der Formel la X nicht Schwefel oder R 1 nicht Thien-2-yl bedeutet, wenn YR 5 für OH steht und R 3 Wasserstoff und R 4 Methyl bedeutet, Verfahren zur Herstellung und herbizide Mittel, die die Verbindungen der Formeln la oder Ib als Wirkstoffe enthalten.Oxazole or thiazolecarboxamides of the formulas Ia and Ib in which the substituents have the following meaning: X oxygen or sulfur; R 1 is hydrogen; Halogen; optionally substituted C 1 -C 6 alkyl, benzyl, cycloalkyl, alkenyl, alkynyl, phenyl, phenoxy or phenylthio; Alkoxy; Alkylthio; Haloalkoxy; Haloalkylthio; or an optionally substituted 5- to 6-membered heterocyclic radical; R 2 formyl, 4,5-dihydrooxazol-2-yl or the radical -COYR 5 ; Y is oxygen or sulfur; R 5 is hydrogen; Cycloalkyl; optionally substituted alkyl, phenyl, benzyl, alkenyl, cycloalkenyl or alkynyl; an optionally substituted 5- or 6-membered heterocyclic radical; Phthalimido; Tetrahydrophthalimido; Succinimido; Maleinimido; one equivalent of a cation; or a residue -N = CR 6 R 7 ; R 6 , R 7 are hydrogen; Alkyl; Cycloalkyl; Phenyl; Furyl or together a methylene chain with 4 to 7 chain links; R 3 is hydrogen or optionally substituted alkyl or cycloalkyl; R 4 hydroxy; Alkoxy; optionally substituted alkyl, cycloalkyl, alkenyl, alkynyl, phenyl or naphthyl; an optionally substituted 5- to 6-membered heterocyclic radical; or R 3 and R 4 together represent a radical of the structure - (CH 2 ) n -Y P - (CH 2 ) q -, where n and q are 1, 2 or 3, p 0 or 1 and Y is oxygen, sulfur or N - Are methyl or form the rest of the formula - (CH 2 ) 3 -CO-, and their environmentally compatible salts, where in the formula Ib X is not sulfur when R 1 is 3-pyridyl, R 2 CO 2 CH 2 CH 3 or R 3 is hydrogen, and in the formula la X is not sulfur or R 1 is not thien-2-yl when YR 5 is OH and R 3 is hydrogen and R 4 is methyl, process for the preparation and herbicidal compositions which comprise the compounds of the formulas Ia or Ib as active ingredients. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11697666-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7645773-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9375008-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112159417-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8815924-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7071355-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5693594-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005049018-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006045350-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1321463-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007082808-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7365094-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7846951-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004056797-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007082808-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8710056-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8729083-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2757856-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9204647-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7915297-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8642597-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9427983-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9125414-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2140865-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112159417-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11767337-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8232302-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011003796-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9029639-B2 |
| priorityDate | 1989-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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