http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002509917-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06 |
| filingDate | 1999-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2002-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2002509917-A |
| titleOfInvention | Use of 2-oxopyrrole as crop protectant and novel 2-oxopyrrole |
| abstract | (57) [Summary]nFormula InEmbedded imagen [However, R 1 Is an aryl or heteroaryl {provided that these groups independently of one another are 1 to 5 of the following groups: hydrogen, halogen, cyano, nitro, hydroxyl, mercapto, thiocyanato, carboxyl, amino, C 1 ~ C 6 Alkyl, C 1 ~ C 6 Cyanoalkyl, C Two ~ C 6 Alkenyl, C 1 ~ C 6 Alkoxy-C Two ~ C 6 Alkenyl, C Three ~ C 6 Alkynyl, C 1 ~ C 6 Alkoxy-C Three ~ C 6 Alkynyl, C Three ~ C 6 Alkynyl-C 1 ~ C 6 Alkoxy, C Three ~ C 7 Cycloalkyl, C 1 ~ C 6 Alkyl-C Three ~ C 7 Cycloalkyl, C 1 ~ C 6 Alkoxy-C Three ~ C 7 Cycloalkyl, C Three ~ C 7 Cycloalkyloxy, C Three ~ C 7 Cyanocycloalkyloxy, C 1 ~ C 6 Alkyl-C Three ~ C 7 Cycloalkyloxy, C Three ~ C 7 Halocycloalkyl, C Three ~ C 7 Cyanocycloalkyl, C Three ~ C 7 Halocycloalkyloxy, C Five ~ C 7 Cycloalkenyl, C 1 ~ C 6 Alkyl-C Five ~ C 7 Cycloalkenyl, C 1 ~ C 6 Alkoxy-C Five ~ C 7 Cycloalkenyl, C Five ~ C 7 Cyanocycloalkenyl, C Five ~ C 7 Halocycloalkenyl, C 1 ~ C 6 Alkoxy-C 1 ~ C 6 Alkyl, C 1 ~ C 6 Haloalkyl, C Two ~ C 6 Haloalkenyl, C Three ~ C 6 Haloalkynyl, C Two ~ C 6 Cyanoalkenyl, C Three ~ C 6 Cyanoalkynyl, C 1 ~ C 6 Alkoxy, C 1 ~ C 6 Cyanoalkoxy, C 1 ~ C 6 Haloalkoxy, C Two ~ C 6 Alkenyloxy, C Two ~ C 6 Cyanoalkenyloxy, C Two ~ C 6 Haloalkenyloxy, C Two ~ C 6 Alkynyloxy, C 1 ~ C 6 Alkylthio, C 1 ~ C 6 Cyanoalkylthio, C 1 ~ C 6 Haloalkylthio, C 1 ~ C 6 Alkoxy-C 1 ~ C 6 Alkylthio, C 1 ~ C 6 Alkoxycarbonyl, C 1 ~ C 6 Alkylcarbonyl, C 1 ~ C 6 Alkylcarboxy-C 1 ~ C 6 Alkyl, C 1 ~ C 6 Alkylcarbonyl-C 1 ~ C 6 Alkyl, C 1 ~ C 6 Alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfonyl, heteroarylsulfinyl, heteroarylsulfonyl, aryl-C 1 ~ C 6 Alkyl, aryl-C Two ~ C 6 Alkenyl, aryl-C Three ~ C 6 Alkynyl, heteroaryl-C 1 ~ C 6 Alkyl, heteroaryl-C Two ~ C 6 Alkenyl, heteroaryl-C Three ~ C 6 Alkynyl, aryl-C 1 ~ C 6 Alkoxy, aryl C Two ~ C 6 Alkenyloxy, aryl-C Three ~ C 6 Alkynyloxy, heteroaryl-C 1 ~ C 6 Alkoxy, heteroaryl-C Two ~ C 6 Alkenyloxy, heteroaryl-C Three ~ C 6 Alkynyloxy, C 1 ~ C 6 Alkylsulfinyl, C 1 ~ C 6 Alkylsulfonyl, C Two ~ C 6 Alkenylsulfinyl, C Two ~ C 6 Alkenylsulfonyl, C 1 ~ C 6 Alkylamino, di-C 1 ~ C 6 Alkylamino, HC = NOH, C 1 ~ C 6 Alkyl-C = NOH, HC = N-O-C 1 ~ C 6 Alkyl, HC = NO-C 1 ~ C 6 Alkyl-aryl, C 1 ~ C 6 Alkyl-C = N-O-C 1 ~ C 6 Alkyl, HC = N-O-C Two ~ C 6 Alkenyl, C 1 ~ C 6 Alkyl-C = N-O-C Two ~ C 6 Alkenyl, HC = N-O-aryl, C 1 ~ C 6 Alkyl-C = NO-aryl, aryl, aryloxy, heteroaryl, heteroaryloxy, arylthio, heteroarylthio may have one to five of these cyclic groups independently of each other. The following groups: hydrogen, halogen, cyano, nitro, hydroxyl, mercapto, thiocyanato, carboxyl, amino, C 1 ~ C 6 Alkyl, C 1 ~ C 6 Cyanoalkyl, C Two ~ C 6 Alkenyl, C 1 ~ C 6 Alkoxy-C Two ~ C 6 Alkenyl, C Three ~ C 6 Alkynyl, C 1 ~ C 6 Alkoxy-C Three ~ C 6 Alkynyl, C Three ~ C 6 Alkynyl-C 1 ~ C 6 Alkoxy, C Three ~ C 7 Cycloalkyl, C 1 ~ C 6 Alkyl-C Three ~ C 7 Cycloalkyl, C 1 ~ C 6 Alkoxy-C Three ~ C 7 Cycloalkyl, C Three ~ C 7 Cycloalkyloxy, C Three ~ C 7 Cyanocycloalkyloxy, C 1 ~ C 6 Alkyl-C Three ~ C 7 Cycloalkyloxy, C Three ~ C 7 Halocycloalkyl, C Three ~ C 7 Cyanocycloalkyl, C Three ~ C 7 Halocycloalkyloxy, C Five ~ C 7 Cycloalkenyl, C 1 ~ C 6 Alkyl-C Five ~ C 7 Cycloalkenyl, C 1 ~ C 6 Alkoxy-C Five ~ C 7 Cycloalkenyl, C Five ~ C 7 Cyanocycloalkenyl, C Five ~ C 7 Halocycloalkenyl, C 1 ~ C 6 Alkoxy-C 1 ~ C 6 Alkyl, C 1 ~ C 6 Haloalkyl, C Two ~ C 6 Haloalkenyl, C Three ~ C 6 Haloalkynyl, C Two ~ C 6 Cyanoalkenyl, C Three ~ C 6 Cyanoalkynyl, C 1 ~ C 6 Alkoxy, C 1 ~ C 6 Cyanoalkoxy, C 1 ~ C 6 Haloalkoxy, C Two ~ C 6 Alkenyloxy, C Two ~ C 6 Cyanoalkenyloxy, C Two ~ C 6 Haloalkenyloxy, C Two ~ C 6 Alkynyloxy, C 1 ~ C 6 Alkylthio, C 1 ~ C 6 Cyanoalkylthio, C 1 ~ C 6 Haloalkylthio, C 1 ~ C 6 Alkoxy-C 1 ~ C 6 Alkylthio, C 1 ~ C 6 Alkoxycarbonyl, C 1 ~ C 6 Alkylcarbonyl, C 1 ~ C 6 Alkylcarboxy-C 1 ~ C 6 Alkyl, C 1 ~ C 6 Alkylcarbonyl-C 1 ~ C 6 Alkyl, C 1 ~ C 6 Alkylcarbonylamino, arylcarbonylamino, arylsulfinyl, arylsulfonyl, heteroarylsulfinyl, heteroarylsulfonyl, aryl-C 1 ~ C 6 Alkyl, aryl-C Two ~ C 6 Alkenyl, aryl-C Three ~ C 6 Alkynyl, heteroaryl-C 1 ~ C 6 Alkyl, heteroaryl-C Two ~ C 6 Alkenyl, heteroaryl-C Three ~ C 6 Alkynyl, aryl-C 1 ~ C 6 Alkoxy, aryl-C Two ~ C 6 Alkenyloxy, aryl-C Three ~ C 6 Alkynyloxy, heteroaryl-C 1 ~ C 6 Alkoxy, heteroaryl-C Two ~ C 6 Alkenyloxy, heteroaryl-C Three ~ C 6 Alkynyloxy, C 1 ~ C 6 Alkylsulfinyl, C 1 ~ C 6 Alkylsulfonyl, C Two ~ C 6 Alkenylsulfinyl, C Two ~ C 6 Alkenylsulfonyl, C 1 ~ C 6 Alkylamino, di-C 1 ~ C 6 Alkylamino, HC = NOH, C 1 ~ C 6 Alkyl-C = NOH, HC = N-O-C 1 ~ C 6 Alkyl, HC = N-O-C 1 ~ C 6 Alkyl-aryl, C 1 ~ C 6 Alkyl-C = N-O-C 1 ~ C 6 Alkyl, HC = N-O-C Two ~ C 6 Alkenyl, C 1 ~ C 6 Alkyl-C = N-O-C Two ~ C 6 Alkenyl, HC = N-O-aryl, C 1 ~ C 6 Alkyl-C = NO-aryl, aryl, aryloxy, heteroaryl, heteroaryloxy, arylthio, optionally having heteroarylthio}, or aryl or heteroaryl is a phenyl ring, C Three ~ C 6 It may be fused with a carbocycle or a 5- or 6-membered heterocycle to form a bicyclic ring system, and the fused ring system may have from 1 to 3 substituents for the above aryl groups. , R Two But C 1 ~ C 6 Alkyl or aryl or heteroaryl {wherein, aryl and heteroaryl are 1 to 3 R 1 May have the substituents mentioned for the aryl. }, C Three ~ C 7 Cycloalkyl or C 1 ~ C 6 A represents alkylaryl, and A represents COOR Three Or CONR Three R Four {Where R Three And R Four Are independently of each other hydrogen, C 1 ~ C 6 Alkyl, C Two ~ C 6 Alkenyl, C Three ~ C 7 Cycloalkyl or C 1 ~ C 6 Alkylaryl (but partially or completely halogenated or C 1 ~ C Four Alkoxy, C 1 ~ C Four Haloalkoxy, C 1 ~ C Four Alkylthio, C Three ~ C 7 Cycloalkyl, C Five ~ C 7 It may have 1 to 3 substituents selected from the group consisting of cycloalkenyl. ). }. And the use of agriculturally useful salts thereof as crop protection agents and novel 2-oxopyrazoles of the formula I. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9012493-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8222430-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010070910-A1 |
| priorityDate | 1998-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 479.