http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2760546-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_173bc2c63b34988699010ba05e5b1376 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C53-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 |
| filingDate | 2016-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2020-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e0c0afb38c007bf9aa74b7ffa400e499 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3867e8c13985f63c93a927fef127155 |
| publicationDate | 2020-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2760546-T3 |
| titleOfInvention | Herbicide compounds |
| abstract | A compound of formula (I) ** Formula ** (I), or a salt or N-oxide thereof, R1 is selected from the group consisting of C1-C4 alkyl, C3-C6 cycloalkyl, C1-C2 alkoxy-alkyl C1-C2, C2-C4 alkenyl, C1-C4 haloalkyl, C2-C4 haloalkenyl, C2-C4 alkynyl and C2-C4 haloalkynyl; R2 is selected from the group consisting of hydrogen, halogen, cyano, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 haloalkoxy, C1-C3 haloalkoxy-C1-C3 alkyl, C1-C6 alkoxy, C1-C3 alkoxy C1-C3 alkyl, C1-C3 alkoxy-C1-C3 alkoxy-C1-C3- alkyl, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C1-C6- hydroxyalkyl, C1- alkylcarbonyl C6-, C1-C6 alkyl-S (O) m-, amino, C1-C6 alkylamino, C1-C6 dialkylamino, -C (C1-C3 alkyl) = NO-C1-C3 alkyl and C2-C6 haloalkynyl; G is hydrogen or C (O) R3; R3 is selected from the group consisting of C1-C6 alkyl, C1-C6 alkenyl, C1-C6 alkynyl, C1-C6 alkoxy, C1-C6 alkyl-S-, -NR4R5, and phenyl optionally substituted with one or more R6; R4 and R5 are independently selected from the group consisting of C1-C6 alkyl and C1-C6 alkoxy, or R4 and R5 together may form a morpholinyl ring; R6 is selected from the group consisting of halogen, cyano, nitro, C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, and C1-C3 haloalkoxy; and T is a 5- or 6-membered monocyclic heteroaryl ring system containing 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen, and sulfur, said 5-membered ring system being substituted with one or more radicals selected from X, Y and R7, and said 6-membered ring system being substituted with one or more radicals selected from X1, X2, X3, X4, and R7, and wherein the oxy-alkyl-D moiety and the pyridazine-dione / pyridazinone moiety are joined by the ring T, so that they are located ortho with respect to each other; or T is a substituted phenyl ring of formula (Tp) ** Formula ** each X, X3, X23 and each Y are independently hydrogen, C1-C3 alkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy or halogen; X1 is oxo, C1-C3 alkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy or halogen; X2 and X4 are independently hydrogen, C1-C3 alkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy, oxo or halogen; X21 is C1-C3 alkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy or halogen; X22 and X24 are independently hydrogen, C1-C3 alkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy or halogen; R7 is hydrogen, C1-C3 alkyl, C1-C3 alkoxy, C1-C3 haloalkyl, C1-C3 haloalkoxy; A indicates the point of adhesion to the oxy-alkyl-D moiety and B indicates the point of adhesion to the pyridazinedione / pyridazinone moiety; and D is a substituted or unsubstituted 5- or 6-membered monocyclic heteroaryl ring containing 1, 2, or 3 heteroatoms independently selected from oxygen, nitrogen, and sulfur, and wherein, when D is substituted, it is substituted on at least one atom. of ring carbon with R8 and / or on a ring nitrogen atom with R9; each R8 is independently oxygen, hydroxyl, halogen, cyano, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 haloalkoxy, C1-C3 haloalkoxy- C1-C3- alkyl, C1-C6 alkoxy, C1-C3 alkoxy-C1 alkyl -C3, C1-C3 alkoxy-C1-C3 alkoxy-C1-C3- alkyl, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C1-C6- hydroxyalkyl, C1-C6 alkylcarbonyl -, C1-C6 alkyl-S (O) m-, amino, C1-C6 alkylamino, C1-C6 dialkylamino, -C (C1-C3 alkyl) = NO-C1-C3 alkyl and C2-C6 haloalkynyl; each R9 is independently, C1-C4 alkyl, C3-C6 alkoxy, C1-C2 alkoxy-C1-C2 alkyl, C2-C4 alkenyl, C1-C4 haloalkyl, C2-C4 haloalkenyl, C2-C4 alkynyl, or C2-C4 haloalkynyl; and m is an integer of 0, 1, or 2. |
| priorityDate | 2015-04-30-04:00^^<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: 558.