http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-101021-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/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-84 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-42 |
| filingDate | 2015-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e64b678abaebbade804d9ef5a1566a7c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99fbc103215ab919b71d70d4d543b763 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75a2bf9a51138a37d38beda228f33afe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa09d9440efa53a9f93b36bc98932b63 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b7d959b90e8c5308e21a5f442d221b8d |
| publicationDate | 2016-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-101021-A1 |
| titleOfInvention | DERIVATIVES OF 2-AMINO-5-CETO-PYRIDIMINE AND ITS USE TO COMBAT INDESATED PLANTAGE GROWTH |
| abstract | Its use in the area of plant protection. Claim 1: Compounds of the general formula (1) and their agrochemically compatible salts in which R¹ is selected from the group consisting of C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ alkylcarbonyl-C₁₋₄ alkyl; C₁₋₆-alkoxycarbonyl-C alquilo-alkyl, C₁₋₆-haloalkoxycarbonyl-C₁₋₆-alkyl, C₁₋₆-alkoxycarbonyl-C₁₋₆-haloalkoxycarbonyl-C₁₋₆-haloalkyl; C₂₋₆ alkenyl, C₂₋₆ haloalkenyl; C₂₋₆ alkynyl, C₂₋₆ haloalkynyl; tri-C₁₋₆-Cils-alkynyl-alkynyl, C₁₋₆-di-C-alkylsilyl, C alqu-C-alkylsilyl-C-alkynyl; C₂₋₆-phenylsilyl-alkynyl; C₆₋₁₄ aryl, which may be substituted in each case in the aryl part with halogen, C₁₋₆ alkyl and / or C₁₋₆ haloalkyl; aryl C₆₋₁₄-C alquilo alkyl; aminocarbonyl-C₁₋₆ alkyl; C₁₋₆-C₁₋₆-alkoxy; C₃₋₈ cycloalkyl, which may be substituted in the cycloalkyl moiety with C₁₋₆ alkyl and / or halogen; C₃₋₈ cycloalkyl-C₁₋₆-alkyl, C₃₋₈-cycloalkyl-C₁₋₆-cycloalkenyl, C₃₋₈-cycloalkenyl-C₁₋₆-cycloalkenyl-C₃₋₈-haloalkyl-C₁₋₆-hydroxy-C₁₋₆-alkyl , cyano-C₁₋₆ alkyl; C₁₋₆-alkylsulfonyl-C₁₋₆-alkyl, C₁₋₆-alkylthio-C₁₋₆-alkyl, C-alkylsulfinyl-C₁₋₆-alkyl, haloalkylsulfonyl-C halo-C alquilo-alkyl, halo-C₁₋₆-alkyl-C₁₋₆-alkyl, C₁₋₆-haloalkylsulfinyl-C alquilo-alkyl, C₁₋₆-alkylsulfonyl-C halo-haloalkyl, C alqu-alkylthio-Cal -alkyl alkyl, C--alkylsulfinyl-C₁₋₆-haloalkyl, C₁₋₆-haloalkylsulfonyl, C₁₋₆ haloalkylthio-C₁₋₆-haloalkyl, C₁₋₆-haloalkylsulfinyl-C₁₋₆-haloalkyl; and R²ᵃ and R²ᵇ, each independently selected from each other from the group consisting of hydrogen, halogen, hydroxy, cyano, nitro, C (O) OH, C (O) NH₂; C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ alkylcarbonyl, C₁₋₆ haloalkylcarbonyl, C₁₋₆ alkylcarbonyloxy, C₁₋₆ haloalkylcarbonyloxy, C₁₋₆ alkylcarbonyl; C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₁₋₆ alkoxycarbonyl, C₁₋₆ haloalkoxycarbonyl, C₁₋₆ alkoxycarbonyl, C₁₋₆ haloalkoxycarbonyl, C alquilo alkoxycarbonyl, C₁₋₆ alkoxycarbonyl, C₁₋₆ haloalkoxycarbonyl-C₁₋₆ haloalkyl; C₂₋₆ alkenyl, C₂₋₆ haloalkenyl, C₂₋₆ alkenylcarbonyl, C₂₋₆ haloalkenylcarbonyl, C₂₋₆ alkenyloxy, C₂₋₆ haloalkenyloxy, C₂₋₆ alkenyloxycarbonyl, C₂₋₆ haloalkenyloxycarbonyl; C₂₋₆ alkynyl, C₂₋₆ haloalkynyl, C₂₋₆ alkynylcarbonyl, C₂₋₆ haloalkynylcarbonyl, C₂₋₆ haloalkyloxy, C₂₋₆ alkyloxycarbonyl, C₂₋₆ haloalkyloxycarbonyl; tri-C₁₋₆-Cils-alkynyl-alkynyl, C₁₋₆-di-C-alkylsilyl, C alqu-C-alkylsilyl-C-alkynyl; C₂₋₆-phenylsilyl-alkynyl; C₆₋₁₄ aryl, C₆₋₁₄ aryloxy, C₆₋₁₄ arylcarbonyl and C₆₋₁₄ aryloxycarbonyl which may each be substituted on the aryl part with halogen, C₁₋₆ alkyl and / or C₁₋₆ haloalkyl; C₆₋₁₄-C₁₋₆-C alquilo-alkyl, C₆₋₁₄-C₁₋₆-alkoxy, C₆₋₁₄-C₁₋₆-carbonyl aryl, C₆₋₁₄-C₁₋₆-carbonyloxy-aryl, C₆₋₁₄-alkoxycarbonyl aryl C₁₋₆, Cil-C-alkoxycarbonyloxy aryl; aminocarbonyl-C₁₋₆-alkyl, di-C-alkylaminocarbonyl-C alquilo-alkyl; N- (haloalkanoyl C₁₋₆) -amino-carbonyl, mono- (aryl C₆₋₁₄) -amino-carbonyl, di- (aryl C₆₋₁₄) -aminocarbonyl; C₁₋₆-C₁₋₆-alkoxy, C₁₋₆-C alco-alkoxy, C₁₋₆-alkoxycarbonyl-C₁₋₆-alkoxy; C₃₋₈ cycloalkyl, which may be substituted in the cycloalkyl moiety with C₁₋₆ alkyl and / or halogen; C₃₋₈ cycloalkoxy, C₃₋₈ cycloalkyl-C₁₋₆ alkyl, C₃₋₈ cycloalkyl-C₁₋₆ -cycloalkyl, C₃₋₈ -cycloalkyl, C₃₋₈ -cycloalkyl-Cal-haloalkoxy, C₃₋₈-cycloalkylcarbonyl, C₃₋₈ cycloalkoxycarbonyl, C₃₋₈ cycloalkyl-C₁₋₆ alkylcarbonyl, C₃₋₈ -cycloalkylcarbonylcarbonyl C₁₋₆, cycloalkylC₃₋₈ -alkoxycarbonyl C₁₋₆, cycloalkyl C₃₋₈-haloalkoxycarbonyl C₁₋₆, cycloalkylcarbonyloxyC₃₋₈, C₃₋₈ cycloalkoxycarbonyloxy, C₃₋₈-cycloalkyl-C₁₋₆-alkylcarbonyloxy, C₁₋₆-cycloalkylcarbonyloxy, C₃₋₈-cycloalkyl-Cx-alkoxycarbonyloxy, C₃₋₈-cycloalkyl-alkoxycarbonyloxy; C₃₋₈ cycloalkenyl, C₃₋₈ cycloalkenyloxy, C₃₋₈ cycloalkenyl-C₁₋₆-alkyl, C ciclo-cycloalkenyl-C₁₋₆ -cycloalkenyl, C alco-C alco-alkoxy, C₃₋₈ -cycloalkenyl-C₁₋₆-haloalkoxy C₃₋₈ cycloalkenylcarbonyl, C₃₋₈ cycloalkenyloxycarbonyl, C₃₋₈ cycloalkenyl C₁₋₆, C₃₋₈ cycloalkenyl C halo-haloalkylcarbonyl C₁₋₆, C₁₋₆ cycloalkenyl-C₃₋₈-haloalkoxycarbonyl C₁₋₆, C₃₋₈ cycloalkenylcarbonyloxy, C₃₋₈ cycloalkenyloxycarbonyloxy, C₁₋₆ cycloalkenyl Cil, C ciclo cycloalkenyl C₁₋₆-haloalkylcarbonyloxy C₁₋₆, C₁₋₆ cycloalkenyl C₁₋₆-C₃₋₈-haloalkoxycarbonyloxy Cilo; hydroxy-C₁₋₆-alkyl, hydroxy-C₁₋₆-alkoxy-C₁₋₆-alkoxy, cyano-C₁₋₆-alkyl; and C₁₋₆ alkylsulfonyl, C₁₋₆ alkylthio, C₁₋₆ alkylsulfinyl, C₁₋₆ haloalkylsulfonyl, C₁₋₆ haloalkylthio, C₁₋₆ haloalkylsulfinyl, C₁₋₆ alkylsulfonyl C-alkyl, C₁₋₆ alkylthio , C₁₋₆-alkylsulfinyl-C alquilo-alkyl, C₁₋₆-haloalkylsulfonyl-C alquilo-alkyl, C₁₋₆-haloalkylthio-C halo-haloalkylsulfinyl-C₁₋₆-alkylsulfonyl-C₁₋₆-haloalkyl , C₁₋₆-C-haloalkyl-C₁₋₆-alkyl, Cul-C-haloalkyl-alkyl, C₁₋₆-haloalkyl sulfonyl-C₁₋₆-haloalkyl, C₁₋₆-haloalkyl-C₁₋₆-haloalkyl-C₁₋₆-haloalkyl-Cfin-haloalkyl , C₁₋₆ alkylsulfonyloxy, C₁₋₆ haloalkylsulfonyloxy, C₁₋₆ alkylthiocarbonyl, C₁₋₆ haloalkylthiocarbonyl, C₁₋₆ alkylthiocarbonyloxy, C₁₋₆ haloalkylthiocarbonyloxy, C₁₋₆ alkylthio, alkylthio C₁₋₆-C₁₋₆ alkoxy, C₁₋₆ alkylthio-C₁₋₆ alkylcarbon, C₁₋₆ alkylthio-Cilt alkylcarbonyloxy; C₄₋₁₄ arylsulfonyl, C₆₋₁₄ arylthio, C₆₋₁₄ arylsulfinyl, C₃₋₈ cycloalkylthio, C₃₋₈ alkenylthio, C₃₋₈ cycloalkenylthio and C₃₋₆ alkynylthio; and R¹ with R²ᵃ can be linked together by means of a bond, so that together with carbons 4 (or carbon 6) and 5 of the pyrimidine and the carbonyl group at position 5 of the pyrimidine it results in a carbocycle or a heterocycle of 5 to 7 partially hydrogenated members that may also be substituted; R³ is selected from the group consisting of hydrogen, C₁₋₆ alkyl C₁₋₆ alkoxy, C₁₋₆ alkoxy-C₁₋₆ alkyl, C₁₋₆-carbonyl alkoxy and aminocarbonyl; R⁴ and R⁵ are each independently selected from each other from the group consisting of hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, hydroxy, C₁₋₆ alkoxy and C₁₋₆ haloalkoxy; or the R⁴ and R⁵ moieties together with the carbon atom to which they are attached, form a ring of three to seven members; and R⁶ and R⁷, each independently selected from each other from the group consisting of hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₆₋₁₄ aryl, C₆₋₁₄ aryloxy, C₆₋₁₄ arylcarbonyl and C₆₋₁₄ aryloxycarbonyl; or the R⁶ and R⁷ moieties together form a C₁₋₇ alkylene group which may contain one or more oxygen and / or sulfur atoms, the C₁₋₇ alkylene group may be mono or polysubstituted with halogen and the respective halogen substituents may be the same or different, and n is the current number 0, 1 or 2 and R⁸, R⁹, R¹⁰ and R¹¹, are each independently selected from each other from the group consisting of hydrogen, halogen, cyano, C (O) OH, C (O ) NH₂, C₁₋₆ alkyl, C₁₋₆ alkylcarbonyl, C₁₋₆ alkyloxycarbonyl, C₁₋₆ alkylaminocarbonyl, C₁₋₆ di-alkylaminocarbonyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₂₋₆ haloalkynyl, C₂₋₆ alkynylcarbonyl, C₂₋₆ haloalkynylcarbonyl, C₂₋₆ haloalkyloxy, C₂₋₆ alkynyloxycarbonyl, C₂₋₆ haloalkyloxycarbonyl and nitro; X represents a bond (in case n = 1 on = 2), CH₂, O, S, carbonyl, NH, CR¹²R¹³ and NR¹⁴ or CH₂O, CH₂S, being that in the two last mentioned groups, the carbon atom is attached to the aromatic part and the heteroatom O or S is attached to the partially hydrogenated part of the amine; and R¹² and R¹³, each independently selected from each other from the group consisting of hydrogen, C₁₋₆ alkyl and C₁₋₆ haloalkyl; and R¹⁴ is selected from the group consisting of hydrogen, C₁₋₆ alkyl and C₁₋₆ haloalkyl. |
| priorityDate | 2014-07-01-04:00^^<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: 32.