http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2417016-T3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_331acb2d2e4707f43b8f6c3cf6f79ab2 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00 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/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 |
| filingDate | 2003-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2013-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2f5edd7269f5b937678601296337a81 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3263c0dda7d8ce8325514ddead11023 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1565c59ea1df6ed18289d8b3a4153b07 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5773dc9a9433fffb1124ba36508ca640 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe3a82edc4bc9eb0ed5f5a40bb13036c |
| publicationDate | 2013-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-2417016-T3 |
| titleOfInvention | Pesticide derivatives of 1-aryl-3-amidoximapyrazol |
| abstract | A compound of formulas (Ia) or (Ib): wherein: R1 is aryl unsubstituted or substituted with one or more radicals R15; X and Y are each independently H, C3-C6 alkenyl, C3-C6 haloalkenyl, C3-C6 alkynyl, C3-C6 haloalkynyl, C3-C7-cycloalkyl-C3-C7-cycloalkyl, -CO2-C1-alkyl -C6, CONR7R8, CONR8R9, -CO2- (CH2) qR7, - (CH2) qR7, - (CH2) qR10, COR8, SO2R13 or COR17; or C1-C6 alkyl unsubstituted or substituted with one or more radicals R11; W is N, C-CH3 or C-halogen; R2 is hydrogen, CH3, or halogen; R3 is halogen, C1-C3 alkyl, C1-C3 halogenoalkyl, C1-C3 halogenoalkoxy, S (O) p-C1-C3 halogenoalkyl or SF5; R4 is H, C3-C6 alkenyl, C3-C6 haloalkyl, C3-C6 alkynyl, C3-C6 haloalkynyl, C3-C7 cycloalkyl, -CO2-C3-C7 cycloalkyl; -CO2-C1-C4-alkyl-C3-C7-cycloalkyl, -CO2-C3-C6-alkenyl, -CO2- (CH2) qR7, CONR8R9, -CO2- (CH2) qR10, - (CH2) qR10, - (CH2) qR10 , COR8 or COCH2O-C1-C4-alkyl; or C1-C6 alkyl unsubstituted or substituted with one or more radicals R11; R5 is H, C2-C6 alkynyl, -CO2-C1-C6 alkyl, C3-C7 cycloalkyl or -SO2R12; or C1-C6-alkyl, C2-C6-alkenyl or CO-C1-C6-alkyl, said last three groups being unsubstituted or substituted with one or more radicals R11; R6 and R13 are each independently C1-C6 alkyl, C1-C6 haloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl or C3-C7 cycloalkyl; R7 is phenyl unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, C1-C6 alkyl, halogenoC1-C6 alkyl, C1-C6 alkoxy, C1-C6 halogenoalkoxy, CN, NO2, S (O) pR13 and NR9R14 ; R8 is H, C1-C6 alkyl, C1-C6 halogenoalkyl, C3-C7 cycloalkyl, -C1-C4 alkyl-C3-C7 cycloalkyl, - (CH2) qR7 or (CH2) qR10; R9 and R14 are each independently H, C1-C6-alkyl, C1-C6-haloalkyl, C3-C7-cycloalkyl or -C1-C4-alkyl-C3-C7-cycloalkyl; or R8 and R9, together with the attached N atom, form a 5- or 6-membered saturated ring optionally containing an additional ring heteroatom which is selected from O, S and N, the ring being unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, C1-C6 alkyl, halogenoC1-C6 alkyl, and halogen; R11 is halogen, C1-C6 alkoxy, C1-C6 halogenoalkoxy, C3-C7 cycloalkyl, S (O) pR13, -CO2-C1-C6-alkyl, -O (C> = O) C1-C6-alkyl, CO-C1-alkyl -C6, CO-C1-C6 halogenoalkyl, NR8R9, CONR8R9, SO2NR8R9, OH, CN, NO2, OR7, NR8COR14, NR8SO2R13 or OR10; R12 is C3-C7 cycloalkyl, C2-C6 alkenyl, C2-C6 haloalkenyl or R10; or phenyl unsubstituted or substituted with one or more radicals selected from R15; or is C1-C6 alkyl unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, C1-C6 alkoxy, halogenoC1-C6 alkoxy, C3-C6 alkylene-oxyl, halogenoC3-C6-oxyl, C3-C6 alkynyl -oxyl, halogenoalquinyl C3-C6-oxyl, cycloalkyl C3-C7, S (O) pR7, S (O) pR10, S (O) pR13, CN, NO2, OH, COR8, NR8COR14, NR8SO2R13, CONR8R9, NR8R9, OR7 , OR10, R16, R10 and CO2R8; R15 is halogen, C1-C6 alkyl, halogeno C1-C6 alkyl, C1-C6 alkoxy, halogeno C1-C6 alkyl, CN, NO2, S (O) pR13, NR8R9, COR13, COR7, CONR8R9, SO2NR8R9, R7, SF5, OH, OR7, R18, OR18, SO3H or C1-C6-imino-alkylidene; R16 is phenyl unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, C1-C6 alkyl, halogenoC1-C6 alkyl, C1-C6 alkoxy, C1-C6 halogenoalkoxy, CN, NO2, S (O) pR13, NR8R9 , COR13, COR7, CONR8R9, SO2NR8R9, OH, SO3H and C1-C6-imino alkylidene; R17 is C1-C5 alkyl which is substituted with C1-C6 alkoxy, S (O) p-C1-C6 alkyl, or S (O) p-C1-C5 halogenoalkyl; R18 is a heteroaromatic radical selected from the group consisting of pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, thienyl, thiazolyl, thiadiazolyl, oxazolyl, isoxazolyl, furyl, pyrrolyl, pyrazolyl, imidazolyl, and substituted with one or plus radicals selected from the group consisting of halogen, C1-C6 alkyl, halogenoC1-C6 alkyl, and C1-C6 alkoxy; m is 1 or 2; n and p are each independently 0, 1 or 2; q is 0 or 1; or a pesticidally acceptable salt thereof. |
| priorityDate | 2002-12-03-04:00^^<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: 416.