http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-103192-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/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D275-03 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D275-03 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 |
| filingDate | 2015-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99fbc103215ab919b71d70d4d543b763 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fcbb87f64b59ff3a9f64154b2bd88e8a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_680666f3375bef565e1eeb26d12fdeb8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bd2711a3d2bcb49c7ddabd7671354261 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a8b0b52f3c0b9a5bbe4fe5f241d98f5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_422191584d03d2924017b6c0af4059ff http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef8a54a2754176acf74ee1583653682a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1dd188796646eb59961b4a32f1e4d66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b7d959b90e8c5308e21a5f442d221b8d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa09d9440efa53a9f93b36bc98932b63 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f9838d8c2ecd0318dd1c3d6626b40b2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5cd990761edf63b000002e04cef25cee http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3fb0bfeadeb6a88ca6374b49ad42a22d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0087b8f917976bff7c78ead95b40a28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a557e072a65306e5b06cfc3ec80cfec5 |
| publicationDate | 2017-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-103192-A1 |
| titleOfInvention | ISOTIAZOLAMIDS, PROCESSES FOR THEIR PREPARATION AND ITS USE AS HERBICIDES AND / OR REGULATORS OF VEGETABLE GROWTH |
| abstract | Herbicides and / or plant growth regulators. Specifically, isothiazolamides, and compositions comprising said isothiazolamides. In addition, processes to prepare said isothiazolamides and their use as herbicides and / or plant growth regulators. Claim 1: Use of one or more compounds of the formula (1) and / or their salts, wherein A is CR⁶R⁷; W is O or S; R¹ is hydrogen, C₁₋₁₂-alkyl, C₁₋₁₂-haloalkyl, C₂₋₁₂-alkenyl, C₂₋₁₂-haloalkenyl, C₂₋₁₂-alkynyl, C₂₋₁₂-haloalkynyl, NR¹³R¹⁴, R¹³R¹⁴N-C₁₋₆-alkyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-haloalkoxy-C₁₋₃-alkyl, C₁₋₆-alkoxy-C₁₋₃-alkyl, C₁₋₆-alkoxy-C₂₋₆-alkoxy-C₁₋ ₃-alkyl, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkylthio-C₁₋₃- alkyl, C₁₋₄-alkylsulfoxy-C₁₋₃-alkyl, C₁₋₄-alkylsulfonyl-C₁₋₃-alkyl, C₁₋₄-haloalkylthio-C₁₋₃-alkyl, C₁₋₄-haloalkylsulfoxy-C₁₋₃-alkyl, C₁₋₄-haloalkylsulfonyl-C₁₋₃-alkyl, C₃₋₁₂-cycloalkyl, C₃₋₈-cycloalkenyl, C₃₋₁₂-cycloalkyl-C₁₋₆-alkyl, C₃₋₈-cycloalkenyl-C₁₋₆-alkyl, C₃₋ ₈-c icloalkoxy, C₃₋₈-cycloalkyl-C₁₋₆-alkoxy, aryl, aryl-C₁₋₃-alkyl, heteroaryl, heteroaryl-C₁₋₃-alkyl, heterocyclyl, heterocyclyl-C₁₋₃-alkyl, aryloxy, heteroaryloxy, heterocyclyloxy, a bicyclic or heterobicyclic residue, where each of the 17 residues mentioned last is not substituted or is substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁ ₋₄-haloalkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄ -haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl , hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N-carbonyl, and dond and the heterocyclyl has q oxo groups, and where each of the mentioned heterocyclic residues, in addition to the carbon atoms, has in each case p members of the ring selected from the group consisting of N (R¹²) ₘ, O and S ( O) ₙ; R² is hydrogen, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₁₋₆-haloalkenyl, C₂₋₆-alkynyl, C₂₋₆-haloalkynyl, C₁₋₄-alkylsulfonyl, C₁₋₄- haloalkylsulfonyl, C₁₋₆-alkylcarbonyl, C₂₋₆-alkenylcarbonyl, C₂₋₆-alkynylcarbonyl, C₁₋₆-haloalkylcarbonyl, C₂₋₆-haloalkenylcarbonyl, C₂₋₆-haloalkynylcarbonyl, C₁₋₆-alkoxycarbonyl, di (C₁₋₆- alkyl) -aminocarbonyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkyl-C₁₋₆-alkyl, C₃₋₈-cycloalkylcarbonyl, C₃₋₈-cycloalkyl-C₁₋₆-alkylcarbonyl, heteroarylcarbonyl, or arylcarbonyl, where each of The 6 residues mentioned last are not substituted or substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy , C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋ ₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N-carbonyl, or R¹ and R², together with the nitrogen atom and (A ) ʸ attached thereto, they form a 5- or 6- membered heterocyclic or heteroaromatic ring, comprising in each case, in addition to the carbon atoms and the nitrogen atom, p ring members selected from the group consisting of N (R¹²) ₘ, O and S (O) ₙ and where said ring is not substituted or is substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁ ₋₄-haloalkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋ ₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆- cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N-carbonyl and has q oxo groups; R³ is hydrogen, halogen, azido, isocyanate, isothiocyanate, nitro, cyano, hydroxyl, NR¹³R¹⁴, triC₁₋₆-alkylsilyl, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₂₋₆-haloalkynyl, C₁₋₆-alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-haloalkoxy-C₁₋₃-alkyl, C₁₋₆-alkoxy-C₁₋₃-alkyl, C₁₋ ₆-alkoxy-C₂₋₆-alkoxy-C₁₋₃-alkyl, C₁₋₆-alkylcarbonyloxy, C₁₋₆-haloalkylcarbonyloxy, C₂₋₆-alkenylcarbonyloxy, C₂₋₆-alkynylcarbonyloxy, C₁₋₄-alkylthio, C₁₋₄- alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkylthio-C₁₋₃-alkyl, C₁₋₄-alkylsulfoxy-C₁₋₃-alkyl, C₁₋₄-alkylsulfonyl-C₁₋₃-alkyl, C₁₋₄-haloalkylthio-C₁₋₃-alkyl, C₁₋₄-haloalkylsulfoxy-C₁₋₃-alkyl, C₁₋₄-haloalkylsulfonyl-C ₋₃-alkyl, C₁₋₆-alkoxycarbonyl, C₁₋₆-haloalkoxycarbonyl, C₂₋₆-alkenyloxycarbonyl, C₂₋₆-haloalkenyloxycarbonyl, C₂₋₆-alkyloxycarbonyl, C₂₋₆-haloalkyloxycarbonyl, C₁₋₆-alkylcarbonyl, C₁₋₆ -haloalkylcarbonyl, C₂₋₆-alkenylcarbonyl, C₂₋₆-haloalkenylcarbonyl, C₂₋₆-alkynylcarbonyl, C₂₋₆-haloalkynylcarbonyl, R¹³R¹⁴N-carbonyl, arylthio, arylsulfoxy, arylsulfonyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkenyl, C₃-cycloalkenyl ₋₈-cycloalkyl-C₁₋₆-alkyl, C₃₋₈-cycloalkenyl-C₁₋₆-alkyl, C₃₋₈-cycloalkoxy, aryl, aryloxy, arylcarbonyloxy, aryl-C₁₋₃-alkyl, heteroaryl, heteroaryloxy, heteroaryl-C₁ ₋₃-alkyl, heterocyclyl, heterocyclyloxy, or heterocyclyl-C₁₋₃-alkyl, where each of the 18 residues mentioned above is not substituted or is substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl , ci ano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄- haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N-carbonyl, and where the heterocyclyl has q oxo groups; R⁴, R⁵ is each independently hydrogen, C₁₋₁₂-alkyl, C₁₋₁₂-haloalkyl, C₂₋₁₂-alkenyl, C₂₋₁₂-haloalkenyl, C₂₋₁₂-alkynyl, C₂₋₁₂-haloalkynyl, C₁₋₆ -alkoxy-C₁₋₃-alkyl, C₁₋₆-alkoxy-C₂₋₆-alkoxy-C₁₋₃-alkyl, C₁₋₆-alkoxy-C₁₋₃-alkylcarbonyl, C₁₋₆-alkoxy-C₂₋₆-alkoxy -C₁₋₃-alkylcarbonyl, C₁₋₆-alkoxycarbonyl, C₁₋₆-haloalkoxycarbonyl, C₂₋₆-alkenyloxycarbonyl, C₂₋₆-haloalkenyloxycarbonyl, C₂₋₆-alkynyloxycarbonyl, C₂₋₆-haloalkyloxycarbonyl, C₁₋₆-alkylcarbonyl, C₁ ₋₆-haloalkylcarbonyl, C₂₋₆-alkenylcarbonyl, C₂₋₆-haloalkenylcarbonyl, C₂₋₆-alkynylcarbonyl, C₂₋₆-haloalkynylcarbonyl, R¹³R¹⁴N-carbonyl, C₁₋₄-alkylthio, C₁₋₄-haloalkylthio, C₁₋₈-alkylthiocarbonyl , C₁₋₈-haloalkylthiocarbonyl, C₁₋₄-alkylsulfoxy, C₁₋₄-haloalkylsulfoxy , C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkylthio-C₁₋₃-alkyl, C₁₋₄-alkylsulfoxy-C₁₋₃-alkyl, C₁₋₄-alkylsulfonyl-C₁₋₃-alkyl, C₁ ₋₄-alkylthio-C₁₋₃-alkylcarbonyl, C₁₋₄-alkylsulfoxy-C₁₋₃-alkylcarbonyl, C₁₋₄-alkylsulfonyl-C₁₋₃-alkylcarbonyl, C₁₋₁₂-alkylcarbonyl, C₁₋₁₂-haloalkylcarbonyl, C₂₋₁₂ -alkenylcarbonyl, C₂₋₁₂-haloalkenylcarbonyl, C₂₋₁₂-alkynylcarbonyl, C₂₋₁₂-haloalkynylcarbonyl, C₁₋₁₂-alkoxycarbonylcarbonyl, C₁₋₁₂-alkoxycarbonyl-C₁₋₃-alkylcarbonyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkenyl , C₃₋₈-cycloalkyl-C₁₋₆-alkyl, C₃₋₈-cycloalkenyl-C₁₋₆-alkyl, C₃₋₈-cycloalkylcarbonyl, C₃₋₈-cycloalkenylcarbonyl, C₃₋₈-cycloalkyl-C₁₋₆-alkylcarbonyl, C₃ ₋₈-cycloalkenyl-C₁₋₆-alkylcarbonyl, aryl, aryl-C₁₋₃-alkyl, hete roaryl heteroaryl-C₁₋₃-alkyl, heterocyclyl, heterocyclyl-C₁₋₃-alkyl, arylcarbonyl, aryl-C₁₋₆-alkylcarbonyl, heteroarylcarbonyl, heteroaryl-C₁₋₆-alkylcarbonyl, heterocyclylcarbonyl, or heterocyclyl-C₁₋₆-alkylcarbonyl, where each of the 20 residues mentioned last is not substituted or is substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁ ₋₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄ -alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁ ₋₄-alkyl, R¹³R¹⁴N-carbonyl, and dond and the heterocyclyl has q oxo groups, where R⁴ and R⁵ are not both an alkyl residue, or NR⁴R⁵ is -N = CR⁸R⁹ or -N = S (O) R¹⁰R¹¹; R⁶, R⁷ are each independently hydrogen, cyano, halogen, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, or C₃₋₈-cycloalkyl, or R⁶ and R⁷, together with the atom of carbon to which they are attached, form a 3- to 6-membered carbocyclic or heterocyclic ring, comprising in each case, in addition to the carbon atoms, p ring members selected from the group consisting of N (R¹²) ₘ, O and S (O) ₙ and where said ring is not substituted or is substituted by one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C alquilo ₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄- alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cic Loalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N-carbonyl and have q oxo groups; R⁸, R⁹ is each independently hydrogen, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₂₋₆-haloalkynyl, C₁₋₆ -alkoxy, C₁₋₆-haloalkoxy, C₁₋₆-haloalkoxy-C₁₋₃-alkyl, C₂₋₆-alkenyloxy, C₂₋₆-haloalkenyloxy, C₂₋₆-alkynyloxy, C₂₋₆-haloalkyloxy, NR¹³R¹⁴, C₁₋₆ -alkoxy-C₁₋₃-alkyl, halogen-C₁₋₆-alkoxy-C₁₋₆-alkyl, C₁₋₆-alkoxy-C₂₋₆-alkoxy-C₁₋₃-alkyl, C₁₋₄-alkylthio-C₁₋₃ -alkyl, C₁₋₄-alkylsulfoxy-C₁₋₃-alkyl, C₁₋₄-alkylsulfonyl-C₁₋₃-alkyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkenyl, C₃₋₈-cycloalkyl-C₁₋₆-alkyl , C₃₋₈-cycloalkenyl-C₁₋₆-alkyl, aryl, aryl-C₁₋₃-alkyl, heteroaryl, heteroaryl-C₁₋₃-alkyl, heterocyclyl, heterocyclyl-C₁₋₃-alkyl, where each of the 10 residues mentioned last term ino is not substituted or is substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy , C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁ ₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N-carbonyl and has q oxo groups, or R⁸ and R⁹, together with the carbon atom to which they are attached, form an unsaturated, partially saturated or saturated ring of 3 to 8 members, comprising in each case, in addition to the carbon atoms, p ring members selected from the group consisting of N (R¹²) ₘ, O and S (O) ₙ and where said ring is not substituted or is substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, C₁ ₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄ -haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N -carbonyl and has q oxo groups; R¹⁰, R¹¹ is each independently C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₂₋₆-haloalkenyl, C₂₋₆-alkynyl, C₂₋₆-haloalkynyl, C₁₋₆-alkoxy -C₁₋₃-alkyl, halogen-C₁₋₆-alkoxy-C₁₋₆-alkyl, C₁₋₆-alkoxy-C₂₋₆-alkoxy-C₁₋₃-alkyl, C₁₋₄-alkylthio-C₁₋₃-alkyl , C₁₋₄-alkylsulfoxy-C₁₋₃-alkyl, C₁₋₄-alkylsulfonyl-C₁₋₃-alkyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkenyl, C₃₋₈-cycloalkyl-C₁₋₆-alkyl, C₃ ₋₈-cycloalkenyl-C₁₋₆-alkyl, aryl, aryl-C₁₋₃-alkyl, heteroaryl, heteroaryl-C₁₋₃-alkyl, heterocyclyl or heterocyclyl-C₁₋₃-alkyl, where each of the 10 residues mentioned in Last term is not substituted or is substituted by one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, C₁ ₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄ -haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N -carbonyl and where the heterocyclyl has q oxo groups, or R¹⁰ and R¹¹, together with the sulfur atom to which they are attached form an unsaturated ring, partially saturated or saturated with 3 to 8 members, which comprises in each case, in addition to the carbon atoms and in addition to the sulfur atom, p ring members selected from the group consisting of N (R¹²) ₘ, O and S (O) ₙ and where said ring is not substituted or is substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NR¹³R¹⁴ , C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁ ₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄ -alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl, R¹³R¹⁴N-carbonyl and has q oxo groups; R¹² is hydrogen, C₁₋₁₂-alkyl, C₁₋₁₂-haloalkyl, C₂₋₁₂-alkenyl, C₂₋₁₂-haloalkenyl, C₂₋₁₂-alkynyl, C₂₋₁₂-haloalkynyl, C₃₋₈-cycloalkyl, C₃₋₈- halocycloalkyl, C₃₋₈-cycloalkenyl, C₃₋₈-cycloalkyl-C₁₋₆-alkyl, C₃₋₈-cycloalkenyl-C₁₋₆-alkyl, C₁₋₁₂-alkylcarbonyl or C₁₋₁₂-haloalkylcarbonyl; R¹³, R¹⁴ is each independently hydrogen, C₁₋₁₂-alkyl, C₁₋₁₂-haloalkyl, C₂₋₁₂-alkenyl, C₂₋₁₂-haloalkenyl, C₂₋₁₂-alkynyl, C₂₋₁₂-haloalkynyl, C₁₋₁₂ -alkylcarbonyl, C₂₋₁₂-alkenylcarbonyl, C₂₋₁₂-alkynylcarbonyl, C₁₋₁₂-haloalkylcarbonyl, C₁₋₄-alkylsulfonyl, C₃₋₈-cycloalkyl, C₃₋₈-cycloalkenyl, C₃₋₈-cycloalkyl-C₁₋₆-alkyl , C₃₋₈-cycloalkenyl-C₁₋₆-alkyl, C₃₋₈-cycloalkylcarbonyl, C₃₋₈-cycloalkenylcarbonyl, C₃₋₈-cycloalkyl-C₁₋₆-alkylcarbonyl, C₃₋₈-cycloalkenyl-C₁₋₆-alkylcarbonyl, aryl , arylcarbonyl, arylsulfonyl, heteroaryl, heteroarylcarbonyl, heteroaryl sulfonyl, heterocyclyl, heterocyclylcarbonyl, heterocyclylsulfonyl, where each of the 17 residues mentioned last is not substituted or substituted with one or more residues of the group consisting of halogen, nitro, hydroxy, cyano, NH₂, C₁₋₆-alkylamine, C₁₋₆-dialkylamine, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋₄-alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋ ₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl-C₁₋₄-alkyl and where the heterocyclyl has q oxo groups, or R¹³ and R¹⁴ , together with the nitrogen atom to which they are attached, form an unsaturated, partially saturated or saturated ring of 3 to 8 members, comprising in each case, in addition to the carbon atoms and in addition to the nitrogen atom, p selected ring members between the group consisting of N (R¹²) ₘ, O and S (O) ₙ and where said ring does not is substituted or substituted with one or more residues of the group consisting of halogen, nitro, hydroxyl, cyano, NH₂, C₁₋₆-alkylamine, C₃₋₆-dialkylamine, C₁₋₄-alkyl, C₁₋₄-haloalkyl, C₁₋₄-alkoxy, C₁₋₄-haloalkoxy, C₁₋₄-alkylthio, C₁₋₄-alkylsulfoxy, C₁₋₄-alkylsulfonyl, C₁₋₄-haloalkylthio, C₁₋₄-haloalkylsulfoxy, C₁₋₄-haloalkylsulfonyl, C₁₋ ₄-alkoxycarbonyl, C₁₋₄-haloalkoxycarbonyl, C₁₋₄-alkylcarboxy, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, C₁₋₄-alkoxycarbonyl-C₁₋₄-alkyl, hydroxycarbonyl, hydroxycarbonyl- C₁₋₄-alkyl and has q oxo groups; n is independently selected from 0, 1 or 2; m is independently selected from 0 or 1; p is independently selected from 0, 1, 2 or 3; q is independently selected from 0, 1 or 2; y is 0 or 1; how |
| priorityDate | 2014-12-22-04:00^^<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: 46.