http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-114976-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_173bc2c63b34988699010ba05e5b1376 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N51-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-647 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-506 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P7-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4439 |
| filingDate | 2019-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_17a6817bfa5e2a59535104d8c2232122 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7ba10e9f77cb3ae6514b406fb613d75 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c21e486eb73c8ea964370449c10168ce http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c0594ed85257279508c8d99cd8b762fb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a35eee8169220ef6e0f503f316395e3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98a4a634c90ecd19279d8cd71592864b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_421b0812f09ab7e12a77fdaee3fd66dd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82b63f796e3fee4ec4c25342bc090c15 |
| publicationDate | 2020-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-114976-A1 |
| titleOfInvention | PESTICIDALLY ACTIVE AZOL-AMIDE COMPOUNDS |
| abstract | The compounds of formula (1), where the substituents are as defined in claim 1, and the agrochemically acceptable salts, stereoisomers, enantiomers, tautomers and N-oxides of these compounds, can be used as insecticides. Claim 1: A compound of formula (1), where: A¹ and A² are independently CR⁵ or N; R¹ is hydrogen, C₁₋₆ alkyl, C₁₋₆ cyanoalkyl, C₁₋₆ aminocarbonylalkyl, C₁₋₆ hydroxycarbonylalkyl, C₁₋₆ nitroalkyl, C₁₋₆ trimethylsilanoalkyl, C₁₋₆ haloalkyl; C₂₋₆ alkenyl, C₂₋₆ haloalkenyl, C₂₋₆ alkynyl, C₂₋₆ haloalkynyl, C₃₋₄ cycloalkyl-C₁₋₂ alkyl, wherein the C₃₋₄ cycloalkyl is optionally substituted with 1 or 2 halogen atoms, oxethane -3-yl-CH₂- or benzyl optionally substituted with halogen or C₁₋₃ haloalkyl; Q is phenyl, pyridine, pyrimidine, pyrazine, or pyridazine, where phenyl, pyridine, pyrimidine, pyrazine, or pyridazine is substituted with R² where n is 1 or 2 and, regardless of ring type, is optionally substituted with Rʸ, where m can be 0, 1 or 2; R² is C₃₋₆ cycloalkyl, phenyl, or heteroaryl, each of which, independently of one another, is optionally substituted with one to three substituents independently selected from Rˣ; OR⁶; piperidin-2-one-1-yl optionally substituted with one to two substituents independently selected from Rˣ; pyridin-2-one-1-yl optionally substituted with one to two substituents independently selected from Rˣ; azetidin-1-yl optionally substituted with one to two substituents independently selected from Rˣ; pyrrolidin-1-yl optionally substituted with one to two substituents independently selected from Rˣ; C₃₋₆cycloalkyl-C₁₋₃ alkyl optionally substituted with one to two substituents independently selected from Rˣ; C₃₋₆ cycloalkyl-C alco alkoxy optionally substituted with one to two substituents independently selected from Rˣ; C₁₋₅ cyanoalkyl; C₁₋₅ cyanoalkoxy; C₁₋₄ alkylsulfonyl optionally substituted with one to two substituents independently selected from Rˣ or C₁₋₄ alkylsulfinyl optionally substituted with one to two substituents independently selected from Rˣ; Rʸ is selected from C₁₋₃ alkyl, C₁₋₃ haloalkyl, C₁₋₃ haloalkylthio, C₁₋₃ alkoxy, C₁₋₃ haloalkoxy, halogen, NO₂, SF₅, CN, C (O) NH₂, C (O) OH and C (S) NH₂; R³ is C₁₋₃ alkyl or C₁₋₃ haloalkyl; R⁴ is pyridine, pyrimidine, pyrazine, or pyridazine, wherein pyridine, pyrimidine, pyrazine or pyridazine is optionally substituted with a substituent selected from: C alqu alkyl, C₁₋₃ haloalkyl, C₁₋₃ alkoxy, C₃₋₄ cycloalkyl, halogen or hydroxyl; R⁵ is hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₃₋₆ cycloalkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkyl, C₁₋₆ alkoxycarbonyl, or di (C₁₋₆ alkoxy) methine; R⁶ is phenyl, benzyl, heteroaryl, or C₃₋₆ cycloalkyl, each of which, independently of one another, is optionally substituted with one to three substituents independently selected from Rˣ; and Rˣ is independently selected from halogen, C₁₋₃ alkyl, C₁₋₃ haloalkyl, C₁₋₃ alkoxy, C₁₋₃ haloalkyl, NO₂, SF₅, CN, CONH₂, C (S) NH₂, C₁₋₄ haloalkylsulfanyl, C₁₋ haloalkylsulfinyl ₄, C₁₋₄ haloalkylsulfonyl, C₁₋₄ alkylsulfanyl, C₁₋₄ alkylsulfinyl, and C₁₋₄ alkylsulfonyl; or N-oxides, tautomers, enantiomers, stereoisomers and agrochemically acceptable salts of the compounds of formula (1). |
| priorityDate | 2018-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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