http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-109821-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/C07D235-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-52 |
| filingDate | 2017-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_085f09e9aef13552e6596e032bc2a276 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_055e32ea4c54e0fc58c1f27a0954942b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9d49aa1146e03bfa6f7698ebddca238 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0feef88a6940fecbf38a242cd938d10b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa8c1b10f648434f51091379eb1f13ff http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de483dc917a3ecaf7dece3dade08ba19 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1602bf93c1f3423571b0951f56895df http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15761e04730c8f82a3e06fe2fc20db3d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d4b1df61a256dc0ad41ef18cb8840c6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c12d37c109f7b824f40b5e83172a096 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6c82ae64a5a381bed0ace7e3830de5a |
| publicationDate | 2019-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-109821-A1 |
| titleOfInvention | DERIVATIVES OF HETEROCICLES AS PESTICIDES |
| abstract | Claim 1: Compounds of the formula (1) characterized in that Q represents C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl-C₃₋₈-alkyl, C₁₋₆-alkyl-C₃₋₈-cycloalkyl, halogenC₁₋₆-Cquil -cycloalkyl-alkyl, alkoxy C₁₋₆-C₃₋₈-cycloalkyl, C₁₋₆-halogen-C₃₋₈-cycloalkyl, C₃₋₈-halogen-cyclo-C₃₋₈-cycloalkyl, or represents aryl or heteroaryl, where appropriate mono- or polysubstituted, equally or differently, where (in the case of hetaryl) it may contain at least one carbonyl group and where substituents are considered in each case: cyano, carboxyl, halogen, nitro, acetyl, hydroxy, amino, SCN, SF₅, tri-alkylsilyl C₁₋₆, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl C₃₋₈, C₁₋₆ alkyl-C₃₋₈ cycloalkyl, halogen C₁₋₆ alkyl-C₃₋₈ cycloalkyl, Cógeno halocycloalkyl, C₃₋₈ cyclocycloalkyl , here C₁₋₆, halogen C₁₋₆ alkyl, C₁₋₆ cyanoalkyl, C₁₋₆ hydroxyalkyl, hydroxycarbonyl-C₁₋₆-alkoxy, C₁₋₆ alkoxycarbonyl-C₁₋₆-alkyl, C₁₋₆-alkoxy-C₁₋₆-alkyl, C₂-alkenyl ₋₆, C₂₋₆ halogenoalkenyl, C₂₋₆ cyanoalkenyl, C₂₋₆ alkynyl, C₂₋₆ haloalkynyl, C₂₋₆ cyanoalkynyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₁₋₆ cyanoalkoxy, C₁₋₆ alkoxycarbonyl ₋₆, C₁₋₆ alkoxy-C₁₋₆ alkoxy, C₁₋₆ alkoxyimino, Cógeno haloalkoxyimino, C alqu alkylthio, C₁₋₆ halogenalkyl, C alco alkoxy-C₁₋₆ alkylthio, C₁₋₆ alkylthio-C₁ alkyl ₋₆, C₁₋₆ alkylsulfinyl, C₁₋₆ halogenoalkylsulfinyl, C₁₋₆ alkoxy-Cul alkylsulfinyl, C₁₋₆ alkylsulfinyl-C₁₋₆ alkyl, C₁₋₆ alkylsulfonyl, C₁₋₆ halogenoalkylsulfonyl, C₁₋₆-alkylsulfonyl C₁ alkoxy ₋₆, alkylsulf C₁₋₆-C₁₋₆-alkyl, Culf-alkylsulfonyloxy, C₁₋₆-halogeno-alkylsulfonyloxy, C₁₋₆-alkylcarbonyl, C₁₋₆ -alkylcarbonyloxy, C₁₋₆-alkoxycarbonyl, C₁₋₆ -alkoxycarbonyl, aminocarbonyl, C₁₋-alkylaminocarbonyl ₆, dialkyl C₁₋₆-aminocarbonyl, halogenalkylaminocarbonyl C₁₋₆, alkenylaminocarbonyl C₂₋₆, dialkenylaminocarbonyl C₂₋₆, cycloalkylaminocarbonyl C₃₋₈, alkylsulfonylamino C₁₋₆, alkylamino C₁₋₆, dialkylamino C₁₋₆, aminosulfonyl, alkylaminosulfonyl C₁₋₆ , C₁₋₆ dialkylaminosulfonyl, C₁₋₆ alkylsulfoximino, aminothiocarbonyl, C₁₋₆ alkylamino-thiocarbonyl, C₁₋₆ dialkylamino-thiocarbonyl, C₃₋₈ cycloalkylamino, NHCO-C₁₋₆ alkyl, NHCO-halogen C₁₋₆, N-C₁ alkyl ₋₄-CO-C₁₋₆ alkyl, N-C₁₋₄-CO-halogen Cal alkyl, NHCO-C₁₋ cycloalkyl ₆, N-C₁₋₄-CO-C ciclo-cycloalkyl alkyl, heteroaryl, oxo-heteroaryl, halogenhetaryl, halogen oxy-heteroaryl, cyano-heteroaryl, cyano-oxo-heteroaryl, halogen C₁₋₆-heteroaryl or halogen C₁₋₆-alkyl oxo-heteroaryl; R⁶ represents C₁₋₆ alkyl, C₁₋₆ cyanoalkyl, C₁₋₆ hydroxyalkyl, C₁₋₆ alkoxy-C₁₋₆ alkyl, halogen C₁₋₆ alkyl, C₂₋₄ alkenyl, C₂₋₄ halogenalkenyl, C₂₋₄ alkynyl, C₂₋ halogen ₄ or C₃₋₈ cycloalkyl; R⁷ represents hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ cyanoalkyl, C₁₋₆ hydroxyalkyl, C₁₋₆ alkoxy-C₁₋₆ alkyl, C₁₋₆ halogenalkoxy-C₁₋₆ alkyl, C₂₋₆ alkenyl, alkenyloxy C₂₋₆-C₁₋₆ alkyl, halogen C₂₋₆-alkyloxyC₁₋₆ alkyl, halogen C₂₋₆, cyanoalkenyl C₂₋₆, alkynyl C₂₋₆, alkynyloxy C₂₋₆-alkyl C₁₋₆, halogenoalkyloxy C₂₋₆-alkyl C₁₋₆, C₂₋₆ halogenoalkynyl, C₂₋₆ cyanoalkynyl, C₃₋₈ cycloalkyl, C₃₋₈ cycloalkyl, C₁₋₆ alkyl C₃₋₈ -cycloalkyl, C₃₋₈ halocycloalkyl, C₁₋₆-alkylthio C₁₋₆, halogen C₁₋₆-C₁₋₆-alkyl alkyl, C alqu alkylsulfinyl-C₁₋₆-alkyl, halogen-C₁₋₆-alkyl-C₁₋₆-alkyl, C₁₋₆-alkylsulfonyl-C₁₋₆-alkyl, halogen-C₁₋₆-alkyl alkylsulfonyl C₁ ₆, C₁₋₆ alkoxy-C₁₋₆-alkylthio-C alquilo-alkyl, Cils-alkoxy-Cils-alkylsulfinyl-C alquilo-alkyl, C₁₋₆-alkoxy-C₁₋₆-alkylsulfonyl-C₁₋₆-alkyl, C₁₋-alkylcarbonyl ₆-C₁₋₆ alkyl, halogen C₁₋₆-alkylcarbonyl-C₁₋₆-alkyl, C alco-alkoxycarbonyl-C₁₋₆-alkyl or halogen-alkoxy-C₁₋₆-carbonyl-C₁₋₆-alkyl; X represents a condensed heteroaromatic, tricyclic or bicyclic system of 9 or 12 members of the series H1 to H15 of the group of formulas (2); R⁸, R⁹ independently of each other represent hydrogen, cyano, halogen, C₁₋₄ alkyl, halogen C₁₋₄ alkyl, Cque alkenyl, C₂₋₄ haloalkenyl, C₂₋₄ alkynyl, C₂₋₄ halogenoalkynyl, C₃₋₆ cycloalkyl, C₃ cycloalkyl ₋₆-C₃₋₆ cycloalkyl, C₁₋₄-alkyl C₃₋₆-cycloalkyl, C₁₋₄-alkyl-C hal-cycloalkyl, Ciano-cyclo-cycloalkyl, C₃₋₆-halogeno-C₁₋₄-alkoxy, C alco-alkoxy, Cógeno-halogenoalkoxy C₁₋₄ alkoxy imino, C₁₋₄ halogenalkoxy imino, C₁₋₄ alkylthio, C₁₋₄ haloalkylthio, C₁₋₄ alkylsulfinyl, Cal haloalkylsulfinyl, C₁₋₄ alkylsulfonyl, halogen Cógeno alkylsulfonyloxy, halogenoalkylsulfonyloxy C₁₋₄, C₁₋₄ alkylcarbonyl, C₁₋₄ haloalkylcarbonyl, aminocarbonyl, C₁₋₄ alkylaminocarbonyl, C₁₋₄-aminocarbonyl dialkyl, alkylsulfonylamino C₁₋₄, C₁₋₄ alkylamino, C₁₋₄ dialkylamino, aminosulfonyl, C₁₋₄ alkylaminosulfonyl or C₁₋₄ dialkylaminosulfonyl; R¹⁰ represents hydrogen, C₁₋₄ alkyl, C₁₋₄ haloalkyl, C₁₋₄ cyanoalkyl, C₁₋₄ hydroxyalkyl, C₁₋₄ alkoxy-C₁₋₄ alkyl, C₁₋₄ halogenalkoxy-C₁₋₄ alkyl, C₂₋₄ alkenyl, alkenyloxy C₂₋₄-C₁₋₄ alkyl, halogen C₂₋₄-alkyloxy-C₁₋₄ alkyl, halogen C₂₋₄, cyanoalkenyl C₂₋₄, alkynyl C₂₋₄, halogenoalkynyl C₂₋₄, cycloalkyl C₃₋₆; and n represents 0, 1 or 2; where for the case that X represents the compound H3 of group of formulas (2), n represents 1 or 2. |
| priorityDate | 2016-10-07-04:00^^<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: 33.