http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-092764-A1
Outgoing Links
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|---|---|
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| filingDate | 2013-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46c207f1b3a7831883960cc381d2e24a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c44a8ff42cb24828ebcb7794055e4c2b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8b6d3874b28455a35aa09780c44aa24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e59e852fa64086a7140f4e3ddd1d8a82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd08522b50f7a6abe2fe15932d613865 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9373b5cd2a121bbd1d4e0ea04cae0179 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af9f46297b34310c4ce08228217c7bfa http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f4e207e97eaabdf8ac76bd95635b4ae http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40733db66d0e11146aa9fc05cc1e52ba http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_acd6993efb4a395ece112a057139c627 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ec61a74176b0f761315d9a3b114472c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b4fb0d3c49de763f280ca31db41ac7b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d59a1690b94b2dc248dc0f5bd8ef595 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6285a39a1b5be6c9bddfaab7bd9f07c9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b2e8471d66c5c7c43c43d3abe5e492e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d8b6fe45618a280bead91b08333a600 |
| publicationDate | 2015-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-092764-A1 |
| titleOfInvention | HETEROCICLICAL COMPOUNDS AS PESTICIDES |
| abstract | Claim 1: Use of the compounds of the formula (1) wherein A represents a radical selected from the group of formulas (2) wherein the dotted line means the bond with Q and wherein A also carries m R² substituents; Q represents a radical selected from the group of formulas (3) where nitrogen is attached to ring A and the arrow means in each case the link with D, and D represents a radical of formula (4) where nitrogen is attached a Q and the arrow means the link with B; B represents a radical selected from the group of formulas (5) where the dotted line means the link with D and where B also carries n substituents R⁷; Y represents CR⁸ or nitrogen; Z represents oxygen or sulfur; R¹ represents a radical of the halogen, cyano, nitro, amino, hydroxy series, represents C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₆ cycloalkyl, C₁₋₆ alkoxy, C₃₋₆-oxy alkenyl , C₃₋₆-oxy alkynyl, C₃₋₆-oxy cycloalkyl, C₁₋₆-carbonyloxy alkyl, C₂₋₆-carbonyloxy alkenyl, C₂₋₆-carbonyloxy alkynyl, C₃₋₆-carbonyloxy cycloalkyl, C₁₋₆-carbonyloxy alkoxy, C₁₋₆-sulfonyloxy alkyl, C₁₋₆-amino alkyl, C₃₋₆-amino alkenyl, C₃₋₆-amino alkynyl, C₃₋₆-amino cycloalkyl, C₁₋₆-carbonylamino alkyl, C₂₋₆-carbonylamino alkenyl, alkynyl C₂₋₆-carbonylamino, C₃₋₆-carbonylamino cycloalkyl, C₁₋₆-carbonylamino alkoxy, C₁₋₆-sulfonylamino alkyl, C₁₋₆-thio alkyl, C₃₋₆-thio alkenyl, C₃₋₆-thio alkynyl, C₃ cycloalkyl ₋₆-thio, C₁₋₆-sulfinyl alkyl, C₁₋₆-sulfonyl alkyl, C₁₋₆-carbonyl alkyl, C₁₋₆-imin alkoxy o-C₁₋₆ alkyl, C₁₋₆-carbonyl alkoxy, aminocarbonyl, C₁₋₆-aminocarbonyl alkyl, di- (C₁₋₆ alkyl) -aminocarbonyl, aminothiocarbonyl, C₁₋₆-aminosulfonyl alkyl, C₁₋₆-sulfonylamino alkyl, C₁₋₆-carbonylamino alkyl, C₁₋₆-thiocarbonylamino alkyl, C₄₋₁₂ bicycloalkyl, aryl, aryloxy, arylamino, arylthio, heteroaryl, heteroaryloxy, heteroarylamino and heteroarylthio where appropriate mono- or polysubstituted, same or different, where the substituents are independently selected from each other of halogen, cyano, nitro, hydroxy, amino, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₃₋₆ cycloalkyl, C₁₋₆ haloalkoxy, C₁₋₆-thio alkyl, aryl, aryloxy, arylthio, heteroaryl, heteroaryloxy and heteroarylthio; R² represents a radical of the halogen, cyano, nitro, amino, hydroxy series, represents C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₆ cycloalkyl, C₁₋₆ alkoxy, C₃₋₆-oxy alken , C₃₋₆-oxy alkyl, C₃₋₈ cycloalkoxy, C₁₋₆-carbonyloxy alkyl, C₂₋₆-carbonyloxy alkenyl, C₂₋₆-carbonyloxy alkynyl, C₃₋₆-carbonyloxy cycloalkyl, C₁₋₆-carbonyloxy alkoxy, C₁ alkyl ₋₆-sulfonyloxy, C₁₋₆-amino alkyl, di- (C₁₋₆ alkyl) -amino, C₃₋₆-amino alkenyl, C₃₋₆-amino alkynyl, C₃₋₆-amino cycloalkyl, C₁₋₆-carbonylamino alkyl , C₂₋₆-carbonylamino alkenyl, C₂₋₆-carbonylamino alkynyl, C₃₋₆-carbonylamino cycloalkyl, C₁₋₆-carbonylamino alkoxy, C₁₋₆-sulfonylamino alkyl, C₁₋₆-thio alkyl, C₃₋₆-thio alkenyl, C₃₋₆-thio alkynyl, C₃₋₆-thio cycloalkyl, C₁₋₆-sulfinyl alkyl, C₁₋₆-sulfonyl alkyl, C₁₋₆-carbonyl alkyl, C₁₋₆-imino-C₁₋₆-alkoxy, C₁₋₆-carbonyl alkoxy, aminocarbonyl, C₁₋₆-aminocarbonyl alkyl, di- (C₁₋₆-alkyl) -aminocarbonyl, aminothiocarbonyl, C₁₋₆-aminosulfonyl alkyl, C₁ alkyl Sulf-sulfonylamino, C₁₋₆-carbonylamino alkyl, C₁₋₆-thiocarbonylamino alkyl, C₄₋₁₂ bicycloalkyl, aryl, aryloxy, arylamino, arylthio, heteroaryl, heteroaryloxy, heteroarylamino, and heteroaryl optionally mono- or polysubstituted, same or different , wherein the substituents are independently selected from halogen, cyano, nitro, hydroxy, amino, C alquilo alkyl, C₁₋₆ alkoxy, C₃₋₆ cycloalkyl, C₁₋₆ haloalkoxy and C₁₋₆ alkyl thio, aryl, aryloxy, arylthio, heteroaryl, heteroaryloxy and heteroarylthio; R³ represents a radical of the hydrogen, halogen, cyano, nitro, amino, hydroxy, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkyl and C₁₋₆ haloalkoxy series; R⁴ represents a radical of the series of hydrogen, halogen, amino, hydroxy, C alquilo alkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkyl and C₁₋₆ haloalkoxy; R⁵ represents a radical of the hydrogen series, C₁₋₆ alkyl, C₃₋₆ cycloalkyl, C₁₋₆ haloalkyl, C₂₋₆ alkenyl, C₃₋₆ alkynyl, C₃₋₆ cycloalkyl-C₁₋₆ alkyl, cyano-C₁₋ alkyl ₆, C₁₋₆-carbonyl alkyl, C₂₋₆-carbonyl alkenyl, C₁₋₆-carbonyl haloalkyl, C₂₋₆-carbonyl haloalkenyl, C₁₋₆-C₁₋₆ alkoxy, C₁₋₆-carbonyl alkoxy, C₁₋ alkyl ₆-sulfonyl and halo-C₁₋₆-sulfonyl alkyl or represents C (= O) -B; R⁶ represents a hydrogen series radical (only in radicals B-26, B-33, B-36 and B-42), halogen, cyano, nitro, amino, hydroxy, carboxyl, represents C₁₋₆ alkyl, alkenyl C₂₋₆, C₂₋₆ alkynyl, C₃₋₆ cycloalkyl, C₁₋₆ alkoxy, C₃₋₆-oxy alken, C₃₋₆-oxy alkyne, C₃₋₆ cycloalkoxy, C₁₋₆-carbonyloxy alkyl, C₂₋₆-alkenyl carbonyloxy, C₂₋₆-alkyloxycarbonyloxy, C₃₋₆-carbonyloxycycloalkyl, C₁₋₆-carbonyloxy alkoxy, C₁₋₆-sulfonyloxy alkyl, C₁₋₆-carbonylamino alkyl, C₂₋₆-carbonylamino alkenyl, C₂₋₆-carbonylamino alkynyl , C₃₋₆-carbonylamino cycloalkyl, C₁₋₆-carbonylamino alkoxy, C₁₋₆-sulfonylamino alkyl, C₁₋₆-thio alkyl, C₁₋₆-sulfinyl alkyl, C₁₋₆-sulfonyl alkyl, C₁₋₆-carbonyl alkyl, C₁₋₆-imino-C₁₋₆-alkoxy, C₁₋₆-carbonyl alkoxy, aminocarbonyl, C₁₋₆-aminocarbonyl alkyl, di- (C₁₋ alkyl ) -aminocarbonyl, aminothiocarbonyl, C₁₋₆-aminosulfonyl alkyl, C₁₋₆-sulfonylamino alkyl, C₁₋₆-carbonylamino alkyl, C₁₋₆-carbonylamino alkyl, C₁₋₆-thiocarbonylamino alkyl, C₄₋₁₂ alkylcycloalkyl, aryl, aryloxy, heteroaryl, heteroaryloxy, if necessary mono- or polysubstituted, the same or different, where the substituents are independently selected from halogen, cyano, nitro, hydroxy, amino, C₁₋₆ alkyl, C₁₋₆ alkoxy, cycloalkyl C₃₋₆, C₁₋₆ haloalkoxy and C₁₋₆-thio alkyl; R⁷ represents a radical of the halogen series, nitro, cyano, amino, hydroxy, represents C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₃₋₆ cycloalkyl, C₁₋₆ alkoxy, C₃₋₆-oxy alken , C₃₋₆-oxy alkyl, C₃₋₆ cycloalkoxy, C₁₋₆-carbonyloxy alkyl, C₂₋₆-carbonyloxy alkenyl, C₂₋₆-carbonyloxy alkynyl, C₃₋₆-carbonyloxy cycloalkyl, C₁₋₆-carbonyloxy alkoxy, C₁ alkyl ₋₆-sulfonyloxy, C₁₋₆-carbonylamino alkyl, C₂₋₆-carbonylamino alkenyl, C₂₋₆-carbonylamino alkynyl, cycloalkyl |
| priorityDate | 2012-10-02-04:00^^<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: 72.