http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-119411-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7f5c2637e6843347aa47a60dcf3fd5ed |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-647 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D237-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D237-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-10 |
| filingDate | 2020-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73818a62ee22b685552a6c3241bc567a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2a6af15f1cfdca8af5d783671836f67 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d981784c46f094c3be12fab29e9bdfe3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0142611a522cc33370c9f2efd958431a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_065b08df71be95210eda5bf0910bda8b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99b835e57421b03c58cdf15439d4d197 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ffcc582db67e06a7fb447afc0fa3480 |
| publicationDate | 2021-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-119411-A1 |
| titleOfInvention | HERBICIDE COMPOUNDS |
| abstract | Claim 1: A compound of formula (1) or a salt or N-oxide thereof, wherein R¹ is selected from the group consisting of C₁₋₄-alkyl, C₃₋₆-cycloalkyl, C₃₋₆-alkoxy, C₁₋₂-alkoxy- C₁₋₂-alkyl, C₂₋₄-alkenyl, C₁₋₄-haloalkyl, C₁₋₄-cyano-alkyl, C₂₋₄-haloalkenyl, C₂₋₄-alkynyl, and C₂₋₄-haloalkynyl; R² is selected from the group consisting of hydrogen, halogen, cyano, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ haloalkoxy, C₁₋₃ haloalkoxy-C₁₋₃ alkyl-, C₁₋₆ alkoxy, C₁₋₃ alkoxy -C₁₋₃-alkyl-, C₁₋₃-alkoxy-C₁₋₃-alkoxy-C₁₋₃-alkyl-, C₃₋₆-cycloalkyl, C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₁₋₆-hydroxyalkyl, hydroxyalkylcarbonyl-, C₁₋₆-, -S(O)ₘ-C₁₋₆-alkyl, amino, C₁₋₆-alkylamino, C₁₋₆-dialkylamino, -C(C₁₋₃-alkyl)=NO-C₁₋₃-alkyl and C₂₋₆-haloalkynyl; G is hydrogen or C(O)R³; R³ is selected from the group consisting of C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋₆-S-alkyl, C₁₋₆ alkoxy, -NR⁴R⁵, and phenyl optionally substituted with one or more R⁶; each R⁴ and R⁵ is independently selected from the group consisting of hydrogen, C₁₋₆ alkyl, C₁₋₆ alkoxy, and C₃₋₆ cycloalkyl, or R⁴ and R⁵ together may form a morpholinyl ring; and, R⁶ is selected from the group consisting of halogen, cyano, nitro, C₁₋₃ alkyl, C₁₋₃ haloalkyl, C₁₋₃ alkoxy, and C₁₋₃ haloalkoxy; X and Y are each independently hydrogen, C₁₋₃ alkyl, cyclopropyl, C₁₋₃ alkoxy, C₁₋₃ haloalkyl, C₁₋₃ haloalkoxy, or halogen; D is a substituted or unsubstituted naphthalene ring system, or a substituted or unsubstituted bicyclic 8-10 membered saturated, partially saturated or unsaturated heterocyclic ring system containing 1, 2, 3 or 4 heteroatoms independently selected from oxygen, nitrogen and sulfur, and wherein, when D is substituted, it is substituted on at least one ring carbon atom by R⁸ and/or on at least one ring nitrogen atom by R⁹; each R⁸ is independently oxygen, hydroxyl, halogen, cyano, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₃₋₆ cycloalkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₁₋₃ alkoxy-C₁₋₃ alkyl, C₁₋ haloalkoxy ₃-C₁₋₃-alkyl-, C₁₋₃-alkoxy-C₁₋₃-alkoxy-C₁₋₃-alkyl-, C₂₋₆ alkenyl, C₂₋₆ haloalkenyl, C₂₋₆ alkynyl, C₂₋₆ haloalkynyl, C₁₋-₋ hydroxyalkyl C₁₋₆-alkylcarbonyl-, C₁₋₆-haloalkylcarbonyl-, C₃₋₆-cycloalkylcarbonyl-, C₁₋₆-alkyl-S(O)ₘ-, -S(O)ₘ-C₁₋₆-haloalkyl, -S(O)ₘ-cycloalkyl C₃₋₆, -OS(O)₂C₁₋₃-alkyl, -C₁₋₃-alkyl-S(O)ₘ-C₁₋₆-alkyl, -C₁₋₃-alkyl-S(O)ₘ-C₁₋₆-haloalkyl, -alkyl C₁₋₃-S(O)ₘ-C₃₋₆-cycloalkyl, cyano-C₁₋₆-alkyl-, -NR⁴R⁵, -C(C₁₋₃-alkyl)=NO-C₁₋₃-alkyl, -C(S)NH₂, alkylaminothiocarbonyl C₁₋₆-, di(C₁₋₆-alkyl)aminothiocarbonyl-, C₃₋₆-cycloalkylamino-thiocarbonylS(O)₂NH₂, -S(O)₂NHC(O)C₁₋₃-alkyl, C₁₋₆-alkylaminosulfonyl-, di(C₁-alkyl ₋₆)aminosulfonyl-, C₃₋₆-cycloalkylamino-sulfonyl-, -C(O)OH, -C(O)O-C₁₋₆-alkyl, -C(O)NHS-(O)₂C₁₋₆-alkyl, -C (O)NR⁴R⁵, -NR⁴C(O)NR⁴R⁵, alkylcar C₁₋₆-bonyl(C₁₋₆-alkyl)amino-, C₁₋₆-haloalkylcarbonylamino-, C₁₋₆-haloalkylcarbonyl(C₁₋₆-alkyl)amino-, C₁₋₆-alkoxycarbonylamino-, C₁₋₆-alkoxycarbonyl(C₁₋₆-alkyl)amino- , C₁₋₆-alkylsulfonylamino-, C₁₋₆-alkylsulfonyl(C₁₋₆-alkyl)amino-, C₁₋₆-haloalkylsulfonylamino-, C₁₋₆-haloalkylsulfonyl(C₁₋₆-alkyl)amino-, C₃₋₆-cycloalkylsulfonylamino-, C₃₃-cycloalkylsulfonyl C₁₋₆-alkyl)amino-, C₁₋₆-alkylaminocarbonylamino-, C₁₋₆-alkylaminocarbonyl(C₁₋₆-alkyl)amino, di(C₁₋₆-alkyl)aminocarbonylamino-, C₁₋₆-haloalkylaminocarbonylamino, C₁₋₆-haloalkylaminocarbonyl C₁₋₆)amino, di(C₁₋₆-haloalkyl)aminocarbonylamino-, di(C₁₋₆-haloalkyl)amino-carbonyl(C₁₋₆-alkyl)amino-, hydroxyamino-, hydroxy(C₁₋₆-alkyl)amino, C₁₋-alkoxyamino ₆, C₁₋₆-alkoxy(C₁₋₆-alkyl)amino, C₁₋₆-haloalkoxyamino, C₁₋₆-haloalkoxy(C₁₋₆-alkyl)amino; or a ring system selected from the group consisting of: a phenyl ring, a 5-6 membered heteroaryl ring and a 3-6 membered heterocyclyl ring, wherein said ring system is substituted with 0 to 5 R¹⁶; m is an integer of 0, 1 or 2; each R⁹ is independently C₁₋₆ alkyl, C₁₋₆ haloalkyl, hydroxy, C₁₋₄ alkoxy, C₁₋₄ alkylthio, C₃₋₆ cycloalkyl, C₁₋₃ alkoxy-C₁₋₃ alkyl, C₁₋₃₋ haloalkoxy-C₁ alkyl -, C₁₋₃-alkoxy-C₁₋₃-alkoxy-C₁₋₃-alkyl-, C₁₋₆-hydroxyalkyl-, -C₁₋₃-alkyl-S(O)ₘ-C₁₋₆-alkyl, -C₁₋₃-alkyl-S(O )ₘ-C₁₋₆-haloalkyl, -C₁₋₃-alkyl-S(O)ₘ-C₃₋₆-cycloalkyl, cyano-C₁₋₆-alkyl-, or a ring system selected from the group consisting of: a phenyl ring, a 5-6 membered heteroaryl ring and a 3-6 membered heterocyclyl ring, wherein said ring system is substituted with 0 to 5 R¹⁶; each R¹⁶ is independently halogen, cyano, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, or C₁₋₆ haloalkoxy; and, W is a compound of the group of formulas (2), where "a" indicates the point of attachment to the phenylpyridazinone/phenylpyridazine moiety, "b" indicates the point of attachment to ring D; R¹⁰, R¹², R¹⁴ and R¹⁵ are each independently hydrogen, C₁₋₃ alkyl, or C₁₋₃ haloalkyl; or R¹⁰ and R¹² together with the carbon atoms to which they are attached form a C₃₋₆ carbocyclic ring; and R¹¹ and R¹³ are each independently hydrogen, halogen, C₁₋₃ alkyl, or C₁₋₃ haloalkyl, with the proviso that when one of R¹¹ or R¹³ is halogen, C₁₋₃ alkyl, or C₁₋₃ haloalkyl, the other is hydrogen. |
| priorityDate | 2019-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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