http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2380051-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/C07D233-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-427 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-427 |
| filingDate | 2006-11-15^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2012-05-08^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9335330bb61d6ae5ccee7ed71e9072c1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c50bc9d70ef8e2f49882e01a88e07f7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8676d05ade3cc86afa8c16fca50c503 |
| publicationDate | 2012-05-08^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2380051-T3 |
| titleOfInvention | Indanyl and tetrahydronaphthyl-amino-azoline compounds to combat animal pests |
| abstract | A tautomeric compound of Indanyl- or Tetrahydronaphthyl-amino-azoline of the formula I wherein n is 1 or 2; m is 1,2,3 or 4, where when m is greater than 1, the radicals R2 can have the same or different meanings X is O or NR3 where R3 is selected from hydrogen, cyano, nitro, formyl, C ( = O) R3c, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl, C1-C6-alkoxy C2-C6-alkylamino, di (C2-C6-alkynyl) amino, (C1-C6-alkoxy) methylene, C1-C6-alkylsulfinyl, C1-C6-alkylsulfenyl or C1-C6-alkylsulfonyl wherein the carbon atoms in the aliphatic radicals of the aforementioned groups can carry any combination of 1, 2 or 3 radicals, independently from each other selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, amino, carboxyl, C1-C6-alkyl, C1-C6-alkoxy, C2-C6-alkenyloxy, C2-C6-alkynyloxy, C1-C6-haloalkoxy and C1-C6-alkylthio, or C (O) NR3aR3b, (SO2) NR3aR3b, phenyl, phenyloxy or benzyl, each of the three radicals mentioned may be unsubstituted or substituted with 1 to 5 radicals, independently one of o tro selected from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkylthio, C1-C6-haloalkylthio, C1-C6-alkoxy and C1-C6-haloalkoxy; and wherein R3a and R3b are each independently hydrogen, C1-C6-alkyl, C1-C6-haloalkyl, C2-C6-alkenyl, or C2-C6-alkynyl. R3c is selected from hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl, C1-C6-alkylthio, C1-C6-alkoxy, (C1-C6-alkyl) amino , di (C1-C6-alkyl) amino, phenyl and heteroaryl, which may be a 5- to 10-membered heteroaromatic, mono or bicyclic ring, containing 1,2,3 or 4 heteroatoms selected from O, S and N; R1 is selected from hydrogen, cyano, nitro, formyl, C (= O) R1c, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl, C1-C6-alkoxy, ( C1-C6-alkoxy) methylene, C1-C6-alkylsulfinyl, C1-C6-alkylsulfenyl or C1-C6-alkylsulfonyl wherein the carbon atoms in the aliphatic radicals of the aforementioned groups can carry any combination of 1, 2 or 3 radicals, independently from each other selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, amino, carboxyl, C1-C6-alkyl, C1-C6-alkoxy, C2-C6-alkenyloxy, C2-C6-alkynyloxy, C1 -C6-haloalkoxy and C1-C6-alkylthio, or C (O) NR1aR1b, (SO2) NR1aR1b, phenyl, phenyloxy or benzyl, each of the three radicals mentioned may be unsubstituted or substituted with 1 to 5 radicals, independently one from another selected from the group consisting of halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C8-alkylthio, C1-C6-haloalkylthio, C1-C6-alkoxy and C1-C6-haloalkoxy; and wherein R1a and R1b are each independently hydrogen, C1-C6-alkyl, C1-C6-haloalkyl, C2-C6-alkenyl, or C2-C6-alkynyl. R1c is selected from hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cydoalkyl, C1-C6-alkylthio, C1-C6-alkoxy, (C1-C6-alkyl) amino , di (C1-C6-alkyl) amino, phenyl and heteroaryl, which may be a 5- to 10-membered heteroaromatic, mono or bicyclic ring, containing 1,2,3 or 4 heteroatoms selected from O, S and N; R2 is selected from halogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxy or C3-C8-cycloalkyl, wherein the radicals can be unsubstituted, partially or completely halogenated; or the enantiomers and / or acceptable salts thereof from the agricultural and / or veterinary point of view, with the proviso that the compound of the formula I is not 2- (4-thio-tert-butyl-1-indanylamino) -oxazoline. |
| priorityDate | 2005-11-25^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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