http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-082828-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_981a37900e6991fb373304ed2ba5a703 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-6518 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-6524 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-10 |
| filingDate | 2011-08-31^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ef20b2e72b440dc4fd4ed76850eec41 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c55f26799802e4aae46ce053f3560628 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1da161522672ad12fb3e7bf2846ec254 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_974b8433ef3f39171ce9e16249caf9f7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67ed82c3a5bee183e4aa7e24cca3a215 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6767ee9415d0cd6f944a316dc525972 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_05ad8c9185e6697ba2cc017a3b3c00fb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffa7418ec5d73e57c879440aa3ea2f8e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_988b0539355e0da0d17000e8a1a295e7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad96dfa845c697ca1abdfd1bc7777301 |
| publicationDate | 2013-01-09^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-082828-A1 |
| titleOfInvention | N- (TETRAZOL-5-IL) - AND N- (TRIAZOL-5-IL) USEFUL ARILCARBOXAMIDS AS HERBICIDES, HERBICIDE COMPOSITIONS THAT CONTAIN THEM AND A PROCEDURE TO CONTROL THE GROWTH OF INDESATED PLANTS |
| abstract | Claim 1: An N- (tetrazol-4-yl) - or N- (triazol-3-yl) arylcarboxamide of the formula (1) or a salt thereof in which A represents N or CY; B represents N or CH; X represents nitro, halogen, cyano, formyl, thiocyanate, C1-6 alkyl, halo C1-6 alkyl, C2-6 alkenyl, C2-6 halo-alkenyl, C2-6 alkynyl, C3-6 halo-alkynyl, C3 cycloalkyl -6, C3-6 halocycloalkyl, C3-6 cycloalkyl-C1-6 alkyl, haloC3-6cycloalkyl C1-6 alkyl, COR1, COOR1, OCOOR1, NR1COOR1, C (O) N (R1) 2, NR1C (O) N (R1) 2, OC (O) N (R1) 2, C (O) NR1OR1, OR1, OCOR1, OSO2R2, S (O) nR2, SO2OR1, SO2N (R1) 2, NR1SO2R2, NR1COR1, C1-6-S (O) nR2 alkyl, C1-6-OR1 alkyl, C1-6-OCOR1 alkyl, C1-6-OSO2R2 alkyl, C1-6-CO2R1 alkyl, C1-6-SO2OR1 alkyl, C1-6 alkyl -CON (R1) 2, C1-6-SO2N alkyl (R1) 2, C1-6-NR1COR1 alkyl, C1-6-NR1SO2R2 alkyl, NR1R2, P (O) (OR5) 2, CH2P (O) (OR5) 2, C1-6 alkyl heteroaryl, C1-6 alkyl heterocyclyl, in which each of the last two radicals mentioned is substituted by halogen radicals, C1-6 alkyl, halo C1-6 alkyl, S (O) n-C1-6 alkyl, C1-6 alkoxy, halo- C1-6 alkoxy, and in which the heterocyclyl has 0 to 2 oxo groups; Y represents hydrogen, nitro, halogen, cyano, thiocyanate, C1-6 alkyl, halo- C1-6 alkyl, C2-6 alkenyl, C2-6 halo-alkenyl, C2-6 alkynyl, C2-6 halo-alkynyl, C3 cycloalkyl -6, C3-6 cycloalkenyl, C3-6 halocycloalkyl, C3-6 cycloalkyl-C1-6 alkyl, haloC3-6cycloalkyl-C1-6 alkyl, COR1, COOR1, OCOOR1, NR1COOR1, C (O) N (R1 ) 2, NR1C (O) N (R1) 2, OC (O) N (R1) 2, CO (NOR1) R1, NR1SO2R2, NR1COR1, OR1, OSO2R2, S (O) nR2, SO2OR1, SO2N (R1) 2 , C1-6-S (O) nR2 alkyl, C1-6-OR1 alkyl, C1-6-OCOR1 alkyl, C1-6-OSO2R2 alkyl, C1-6-CO2R1 alkyl, C1-6-CN alkyl, C1- alkyl 6-SO2OR1, C1-6-CON alkyl (R1) 2, C1-6-SO2N alkyl (R1) 2, C1-6-NR1COR1 alkyl, C1-6-NR1SO2R2 alkyl, N (R1) 2, P (O) (OR5) 2, CH2P (O) (OR5) 2, C 1-6 alkyl phenyl, C 1-6 alkyl heteroaryl, C 1-6 alkyl heteroaryl, C 1-6 alkyl heterocyclyl, phenyl, heteroaryl or heterocyclyl, in the that each of the last 6 radicals mentioned is substituted with s radicals of the group consisting of halogen, nitro, cyano, C1-6 alkyl, halo-alkyl or C1-6, C3-6 cycloalkyl, S (O) n-C1-6 alkyl, C1-6 alkoxy, halo C1-6 alkoxy, C1-6 alkoxy-C1-4 alkyl and cyanomethyl, and in which the heterocyclyl has 0 to 2 oxo groups; Z represents halogen, cyano, thiocyanate, halo C1-6 alkyl, C2-6 alkenyl, C2-6 halo-alkenyl, C2-6 alkynyl, halo C2-6 alkynyl, C3-6 cycloalkyl, C3-6 halocycloalkyl , C3-6 cycloalkyl-C1-6 alkyl, halo-C3-6 -cycloalkyl-C1-6 alkyl, COR1, COOR1, OCOOR1, NR1COOR1, C (O) N (R1) 2, NR1C (O) N (R1) 2 , OC (O) N (R1) 2, C (O) NR1OR1, OSO2R2, S (O) nR2, SO2OR1, SO2N (R1) 2, NR1SO2R2, NR1COR1, C1-6-S (O) nR2 alkyl, C1 alkyl -6-OR1, C1-6-OCOR1 alkyl, C1-6-OSO2R2 alkyl, C1-6-CO2R1 alkyl, C1-6-SO2OR1 alkyl, C1-6-CON (R1) 2 alkyl, C1-6-SO2N alkyl (R1) 2, C1-6-NR1COR1 alkyl, C1-6-NR1SO2R2 alkyl, N (R1) 2, P (O) (OR5) 2, heteroaryl, heterocyclyl or phenyl, in which each of the last three radicals mentioned above is substituted by radicals of the group consisting of halogen, nitro, cyano, C1-6 alkyl, halo- C1-6 alkyl, cycloalkylC3-6, S (O) n-C1-6 alkyl, C1-6 alkoxy and C1-6 halo-alkoxy, and in which the heterocyclyl has 0 to 2 oxo groups, or Z may also represent hydrogen, alkyl C1-6 yl or C1-6 alkoxy if Y represents the radical S (O) nR2; R represents C1-6 alkyl, C3-7 cycloalkyl, halo- C1-6 alkyl, C2-6 alkenyl, C2-6 halo-alkenyl, C2-6 alkynyl, C2-6 halo-alkynyl, CH2R6, heteroaryl, heterocyclyl or phenyl , wherein each of the last three radicals mentioned is substituted with s radicals of the group consisting of halogen, nitro, cyano, C1-6 alkyl, halo- C1-6 alkyl, C3-6 cycloalkyl, S (O) n -C 1-6 alkyl, C 1-6 alkoxy, C 1-6 halo-alkoxy, C 1-6 alkoxy-C 1-4 alkyl; R1 represents hydrogen, C1-6 alkyl, C1-6 haloalkyl, C2-6 alkenyl, C2-6 haloalkenyl, C2-6 alkynyl, C2-6 haloalkynyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, C3-6 halocycloalkyl, alkyl C1-6-O-C1-6 alkyl, C3-6 cycloalkyl-C1-6 alkyl, phenyl, phenyl-C1-6 alkyl, heteroaryl, C1-6 alkyl-heteroaryl, heterocyclyl, C1-6 alkyl-heterocyclyl, C1 alkyl -6-O-heteroaryl, C1-6-O-heterocyclyl alkyl, C1-6-NR3-heteroaryl alkyl, C1-6-NR3-heterocyclyl alkyl, in which each of the last 21 radicals mentioned is substituted with radicals from the group consisting of cyano, halogen, nitro, thiocyanate, OR3, S (O) nR4, N (R3) 2, NR3OR3, COR3, OCOR3, SCOR4, NR3COR3, NR3SO2R4; CO2R3, COSR4, CON (R3) 2 and C1-4 alkoxy-C2-6 alkoxycarbonyl, and in which the heterocyclyl has 0 to 2 oxo groups; R 2 represents C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 haloalkenyl, C 2-6 alkynyl, C 2-6 haloalkynyl, C 3-6 cycloalkyl, C 3-6 cycloalkenyl, C 3-6 halocycloalkyl, C 1-6 alkyl 6-O-C 1-6 alkyl, C 3-6 cycloalkyl-C 1-6 alkyl, phenyl, phenyl-C 1-6 alkyl, heteroaryl, C 1-6 alkyl-heteroaryl, heterocyclyl, C 1-6 alkyl-heterocyclyl, C 1-6 alkyl -O-heteroaryl, C1-6-O-heterocyclyl alkyl, C1-6-NR3-heteroaryl alkyl, C1-6-NR3-heterocyclyl alkyl, in which each of the last 21 radicals mentioned is substituted with radicals of the group consisting of cyano, halogen, nitro, thiocyanate, OR3, S (O) nR4, N (R3) 2, NR3OR3, COR3, OCOR3, SCOR4, NR3COR3, NR3SO2R4, CO2R3, COSR4, CON (R3) 2 and C1-alkoxy C2-6 4-alkoxycarbonyl, and in which the heterocyclyl has 0 to 2 oxo groups; R3 represents hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl or C3-6 cycloalkyl-C1-6 alkyl; R4 represents C1-6 alkyl, C2-6 alkenyl or C2-6 alkynyl; R5 represents methyl or ethyl; R6 represents acetoxy, acetamido, N-methylacetamido, benzoyloxy, benzamido, N-methylbenzamido, methoxycarbonyl, ethoxycarbonyl, benzoyl, methylcarbonyl, piperidinylcarbonyl, morpholinylcarbonyl, trifluoromethylcarbonyl, aminocarbonyl, methylaminocarbonyl, dimethylaminocarbonyl, C1-6 alkoxy, C3-6 cycloalkyl or heteroaryl represents , heterocyclyl or phenyl, each of which is substituted with radicals of the group consisting of methyl, ethyl, methoxy, trifluoromethyl and halogen; n represents 0, 1 or 2; s represents 0, 1, 2 or 3; with the proviso that none of X and Z represents chlorine and B does not represent nitrogen if R represents n-propyl. |
| priorityDate | 2010-09-01^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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