http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2694200-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0bf0928b608797b70bbc2b91c7e52e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80 |
| classificationIPCInventive | 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/C07D257-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-14 |
| filingDate | 2013-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2018-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f563ee76724805c7105f241eeacb1e6c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7eefb0e8db7580dd821642045428e94 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1709f66e5bd0b424e005b7beb1c403d7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5344f02df01770dfcba3c76709d8f82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7b8d175a7581cf8d9386a294f26c047 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e6d5b9182fbb582592377ff01d064ab http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5eb7e40053b585f0142f9d0c8ff1a855 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6cf54d776d46b86f572bab628f0af255 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ae87d518384ecc1aa4610e06cac8354 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_807a7c6926bc5488085496d4a1f66805 |
| publicationDate | 2018-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2694200-T3 |
| titleOfInvention | Compounds of substituted N- (tetrazol-5-yl) and N- (triazol-5-yl) arylcarboxamide and their use as herbicides |
| abstract | N- (tetrazol-5-yl) - and N- (triazol-5-yl) arylcarboxamides of formula I, ** Formula ** wherein B is N or CH; R is selected from the group consisting of hydrogen, C1-C6-alkyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, where the C3-C7 cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or totally halogenated, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C1-C4-alkoxy-C1-C4-alkyl, C1- C4-haloalkoxy-C1-C4-alkyl, Rb-S (O) n-C1-C3-alkyl, Rc-C (> = O) -C1-C3-alkyl, RdO-C (> = O) -C1- C3-alkyl, ReRfN-C (> = O) -C1-C3-alkyl, RgRhN-C1-C3-alkyl, phenyl-Z and heterocyclyl-Z, where heterocyclyl is an aromatic, partially unsaturated or monocyclic aromatic heterocycle of 5 or 6 members or 8, 9 or 10 members, containing 1, 2, 3 or 4 heteroatoms as ring members, which are selected from the group consisting of O, N and S, where phenyl and heterocyclyl are unsubstituted or substituted with 1, 2, 3 or 4 R 'groups, which are identical or different; R1 is selected from the group consisting of cyano-Z1, halogen, nitro, C1-C6-alkyl, C2-C8-alkenyl, C2-C8-alkynyl, C1-C8-haloalkyl, C1-C8-alkoxy, C1-C4- C1-C4-alkoxy-C1-C4-C1-C4-alkoxy-Z1, C1-C4-alkyl-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkylthio-Z1, C2- C6-alkenyloxy, C2-C6-alkynyloxy, C1-C6-haloalkoxy, C1-C4-haloalkoxy-C1-C4-alkyl, C1-C4-haloalkoxy-C1-C4-alkoxy-Z1, R1b-S (O) kZ1, phenoxy-Z1, and heterocyclyloxy-Z1, where heterocyclyloxy is a 5- or 6-membered or 5, 9 or 10-membered monocyclic aromatic heterocyclic, or oxygen-linked heterocycle, containing 1, 2, 3 or 4 heteroatoms as ring members, which are selected from the group consisting of O, N and S, where the cyclic groups in phenoxy and heterocyclyloxy are unsubstituted or substituted with 1, 2, 3 or 4 R11 groups, which are identical or different; R2, R3 are identical or different and are independently selected from the group consisting of hydrogen, halogen, OH-Z2, NO2-Z2, cyano-Z2, C1-C6-alkyl, C2-C8-alkenyl, C2-C8-alkynyl, C3-C10-cycloalkyl-Z2, C3-C10-cycloalkoxy-Z2, where the C3-C10 cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or totally halogenated, C1-C8-haloalkyl, C1-C8-alkoxy- Z2, C1-C8-haloalkoxy-Z2, C1-C4-alkoxy-C1-C4-alkoxy-Z2, C1-C4-alkylthio-C1- C4-alkylthio-Z2, C2-C8-alkenyloxy-Z2, C2-C8- alkynyloxy-Z2, C2-C8-haloalkenyloxy-Z2, C2-C8-haloalkyloxy-Z2, C1-C4-haloalkoxy-C1-C4-alkoxy-Z2, (tri-C1-C4-alkyl) silyl-Z2, R2b-S (O) k-Z2, R2c-C (> = O) -Z2, R2dO-C (> = O) -Z2, R2eR2f NC (> = O) -Z2, R2gR2hN-Z2, phenyl-Z2a and heterocyclyl-Z2a , where heterocyclyl is an aromatic, partially unsaturated or monocyclic aromatic heterocycle of 3, 4, 5 or 6 members or monocyclic of 8, 9 or 10 members., which contains 1, 2, 3 or 4 heteroatoms as ring members, which are s choose from the group consisting of O, N and S, where the cyclic groups in phenyl-Z2a and heterocyclyl-Z2a are unsubstituted or substituted with 1, 2, 3 or 4 R21 groups, which are identical or different; R4 is selected from the group consisting of hydrogen, halogen, cyano, nitro, C1-C4-alkyl and C1-C4-haloalkyl; R5 is selected from the group consisting of halogen, C1-C4-alkyl and C1-C4-haloalkyl; n is 0, 1 or 2; k is 0, 1 or 2; R ', R11, R21 independently from each other are selected from the group consisting of halogen, NO2, CN, C1-C6-alkyl, C3-C7-cycloalkyl, C3-C7-halocycloalkyl, C1-C6-haloalkyl, C2-C6- alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C1-C6-alkoxy, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-haloalkoxy-C1-C4-alkyl, C1-C4-alkoxy-C1-C4-alkoxy, C3-C7-cycloalkoxy and C1-C6-haloalkyloxy, or two neighboring radicals R ', R11or R21 together can form a group > = O; Z, Z1, Z2 independently of each other are selected from the group consisting of a covalent bond and C1-C4-alkanediyl; Z2a is selected from the group consisting of a covalent bond, C1-C4-alkanediyl, O-C1-C4-alkanediyl, C1-C4-alkanediyl-O and C1-C4-alkanediyl-O-C1-C4-alkanediyl; Rb, R1b, R2b independently from each other are selected from the group consisting of C1-C6-alkyl, C3-C7-cycloalkyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl , C2-C6-haloalkynyl, phenyl and heterocyclyl, where heterocyclyl is a saturated, partially unsaturated or aromatic 5 or 6 membered monocyclic heterocycle, containing 1, 2, 3 or 4 heteroatoms as ring members, which are selected from the group that It consists of O, N and S, where phenyl and heterocyclyl are unsubstituted or substituted with 1, 2, 3 or 4 groups, which are identical or different and are selected from the group consisting of halogen, C1-C4-alkyl, C1- C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy; Rc, R2c independently from each other are selected from the group consisting of hydrogen, C1-C6-alkyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, where the C3-C7 cycloalkyl groups in the two The aforementioned radicals are unsubstituted or partially or totally halogenated, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C1-C4-alkoxy-C1- C4-alkyl, phenyl, benzyl and heterocyclyl, where heterocyclyl is a saturated 5- or 6-membered monocyclic heterocycle, partially unsaturated or aromatic, containing 1, 2, 3 or 4 heteroatoms as ring members, which are selected from the group consisting in O, N and S, where phenyl, benzyl and heterocyclyl are unsubstituted or substituted with 1, 2, 3 or 4 groups, which are identical or different and are selected from the group consisting of halogen, C1-C4-alkyl, C1 -C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy; Rd, R2d independently from each other are selected from the group consisting of C1-C6-alkyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, where the C3-C7 cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or fully halogenated, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C1-C4-alkoxy-C1-C4-alkyl , phenyl and benzyl, where phenyl and benzyl are unsubstituted or substituted with 1, 2, 3 or 4 groups, which are identical or different and are selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl , C1-C4-alkoxy and C1-C4-haloalkoxy; Re, Rf independently from each other are selected from the group consisting of hydrogen, C1-C6-alkyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, where the C3-C7 cycloalkyl groups in the two radicals Above mentioned are unsubstituted or partially or totally halogenated, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C1-C4-alkoxy-C1-C4 -alkyl, phenyl and benzyl, where phenyl and benzyl are unsubstituted or substituted with 1, 2, 3 or 4 groups, which are identical or different and are selected from the group consisting of halogen, C1-C4-alkyl, C1-C4 -haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy, or Re, Rf together with the nitrogen atom, to which they are attached can form a 5, 6 or 7-membered N-linked heterocyclic radical, saturated or unsaturated, which may carry an additional heteroatom selected from O, S and N as a member of the ring and which is not substituted or that may carry 1, 2, 3 or 4 groups, which are identical os or different and are selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy; R2e, R2f independently of each other have the meanings given for Re, Rf; Rg is selected from the group consisting of hydrogen, C1-C6-alkyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, where the C3-C7 cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or totally halogenated, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C1-C4-alkoxy-C1-C4-alkyl, phenyl and benzyl, where phenyl and benzyl are unsubstituted or substituted with 1, 2, 3 or 4 groups, which are identical or different and are selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1- C4-alkoxy and C1-C4-haloalkoxy; Rh is selected from the group consisting of hydrogen, C1-C6-alkyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, where the C3-C7 cycloalkyl groups in the two aforementioned radicals are unsubstituted or partially or fully halogenated, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C1-C4-alkoxy-C1-C4-alkyl, to radical C (> = O) -Rk, phenyl and benzyl, where phenyl and benzyl are unsubstituted or substituted with 1, 2, 3 or 4 groups, which are identical or different and are selected from the group consisting of halogen, C1-C4 -alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy, or Rg, Rh together with the nitrogen atom, to which they are attached can form an N-linked heterocyclic radical of 5, 6 or 7 members, saturated or unsaturated, which may carry as an ring member an additional heteroatom selected from O, S and N and which is not substituted or which may carry 1, 2, 3 or 4 groups, which are identical or different s and are selected from the group consisting of> = O, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy; R2g, R2h independently of each other have the meanings given for Rg, Rh; Rk has the meanings given for Rc; an N-oxide or an appropriate agricultural salt thereof. |
| priorityDate | 2012-04-27-04:00^^<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: 1743.