http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-107545-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cb64e9c79e4024fa943a53a54161a86f |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01G7-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N55-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N57-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N63-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-18 |
| filingDate | 2017-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7216025f8b305a293561747faa73d0bc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce25a3cada2828dcc03a6fc3924cae53 |
| publicationDate | 2018-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-107545-A1 |
| titleOfInvention | FUNGICIDE COMPOSITION |
| abstract | Claim 1: A fungicidal composition characterized in that it comprises: (a) at least one of a compound of the formula (1) {wherein T is CH or a nitrogen atom; R¹ is a hydrogen atom, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, a halogen, cyano or hydroxy atom; each of R², R³, R⁴ and R⁵ is, independently, a hydrogen atom, C₁₋₆ alkyl, C₃₋₆ cycloalkyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, a halogen atom , cyano or hydroxyl or R² together with R³ and R⁴ together with R⁵, are taken, independently, together with a carbon atom to which they are attached, to form a carbonyl group (C = O); each occurrence of R⁶ is, independently, oxo, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, a halogen, cyano or hydroxy atom; n is 0-2; each of X¹, X², X³ and X⁴ is, independently, a hydrogen atom, a halogen atom, cyano, hydroxy, nitro, formyl, mercapto, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl , C₁₋₆ haloalkyl, C₂₋₆ haloalkenyl, C₂₋₆ haloalkynyl, C₁₋₆ alkoxy, C₂₋₆-oxy alkenyl, C₂₋₆-oxy alkynyl, C₁₋₆ haloalkoxy, C₂₋₆-oxi haloalkenyl, C₂₋ haloalkynyl Ox-oxy, carboxy, carbamoyl, C₃₋₆ cycloalkyl, C₃₋₈ halocycloalkyl, C₃₋₆ cycloalkoxy, C₃₋₈ halocycloalkoxy, C₂₋₆ alkoxyalkyl C₄₋₁₀ haloalkoxyalkyl C₂₋₆, halocycloalkoxyalkyl C₄₋₁₀, alkoxyalkoxyalkyl C₃₋ ₈, C₂₋₆ alkoxyalkoxy, C₄₋₁₀ cycloalkylalkoxy, C₁₋₆ hydroxyalkyl, C₄₋₁₀ cycloalkylalkyl, C₄₋₁₀ alkylcycloalkyl, C₆₋₁₄ cycloalkyl alkyl, C₄₋₁₀ halocycloalkylalkyl, C₆₋₁₄ halocycloalkyl alkyl, C₄₋₁₀ haloalkylcycloalkyl, C₅₋₁₀ alkylcycloalkylalkyl, C₃₋₈ cycloalkenyl, C₃₋₈ halocycloalkenyl, -SR²⁵, -S (O) R²⁵, -S (O) ₂R²⁵, -OS (O) ₂R²⁵, - (C₁₋₆ alkyl ) S (O) ₂R²⁵, Cilt alkylthioalkyl, C₂₋₆ alkylsulfinyl alkyl, C₂₋₆ alkylsulfonylalkyl, C₂₋₆ alkylcarbonyl, C₂₋₆ haloalkylcarbonyl, C₄₋₈ cycloalkylcarbonyl, C₂₋₆-carbonyl alkoxy, C₂₋₆ haloalkoxycarbonyl , C₄₋₈-carbonyl cycloalkoxy, C₅₋₁₀-alkoxycarbonyl cycloalkyl, C₂₋₆-carbonyloxy alkyl, C₂₋₆-carbonyloxy alkyl, C₄₋₈-carbonyloxycycloalkyl, C₂₋₆-carbonyloxy alkoxy, C₂₋₆-carbonyloxy haloalkoxy, C₄₋₈-carbonyloxy cycloalkoxy, C₃₋₆-carbonylalkoxy alkyl, -NR²⁶R²⁷, C₂₋₆-aminoalkyl alkyl, (dialkylamino) C₃₋₈ alkyl, C₂₋₆ haloalkylaminoalkyl, C₄₋₁₀ cycloalkylaminoalkyl, C₁₋₆-sulfonylamino alkyl, haloalkyl C₁ ₋₆-sulfonylamino, C₂₋₆-aminocarbonyl alkyl, (dialkyl C₃₋₁₀-amino) carbonyl, C₄₋₈-aminocarbonyl cycloalkyl, (N-alkoxy-N-alkyl) amino C₂₋₈, (dialkylamino) oxyC₂₋₈ , trialkyl C₃₋₁₀-hydrazinyl, trialkyl C₃₋₁₀-silyl, trialkyl C₄₋₁₀-silylalkyl, trialkyl C₅₋₁₀-silylalkynyl, trialkyl C₃₋₁₀-silyloxy, trialkyl C₄₋₁₂-silyl-alkoxy, trialkyl C₅₋₁₂-silyl-alkoxyalkyl, Cquil-silylalkyloxy trialkyl, C₂₋₆-sulfonyloxyalkyl alkyl, C₂₋₆-sulfonyloxyalkyl haloalkyl, -C (= NOR²⁸) R²⁹, -C (= NR³⁰) R²⁹, C₂₋₆ cyanoalkyl, phenyl, phenoxy or benzyl or X¹ together with X², X² together with X³ and X³ together with X⁴ form a C₂₋₆ alkylene chain that can contain an oxygen atom, a sulfur atom or -NR³¹- or are taken together with a carbon atom to which they are attached, to form a thiophene ring, a pyridine ring, a pyrrole ring, an imi ring dazol, a benzene ring, a naphthalene ring, a pyrimidine ring, a furan ring, a pyrazine ring, a pyrazole ring or an oxazole ring; R²⁵ is C₁₋₈ alkyl, C₃₋₈ cycloalkyl, C₁₋₆ haloalkyl, C₃₋₈ halocycloalkyl, C₁₋₆-amino alkyl, phenyl or benzyl and phenyl or benzyl may be substituted with at least one R³²; R³² is C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₁₋₆ haloalkyl, C₁₋₆ alkoxy, C₃₋₈ haloalkoxy, C₃₋₈ halocycloalkyl, C₁₋₆-thio alkyl, C₁₋₆-sulfinyl alkyl , C₁₋₆-sulfonyl alkyl, C₁₋₆-thio haloalkyl, C₁₋₆-sulfinyl haloalkyl, C₁₋₆-sulfonyl haloalkyl, a halogen, cyano or hydroxy atom; each of R²⁶ and R²⁷ is, independently, a hydrogen atom, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₁₋₆ haloalkyl, C₃₋₈ halocycloalkyl, C₁₋₆ alkoxy, C₂₋₈-amino dialkyl, alkyl C₂₋₆-carbonyl, C₂₋₆ haloalkylcarbonyl, C₄₋₈ cycloalkylcarbonyl, C₂₋₆-carbonyl alkoxy, C₂₋₆-carbonyl haloalkoxy or (C₃₋₁₀-amino) carbonyl dialkyl; R²⁸ is a hydrogen atom, C₁₋₆ alkyl, C₁₋₆ haloalkyl or benzyl; R²⁹ is a hydrogen atom, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₁₋₆ haloalkyl, C₃₋₈ halocycloalkyl, C₄₋₁₀ cycloalkylalkyl, phenyl or benzyl; R³⁰ is C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₁₋₆ haloalkyl, C₃₋₈ halocycloalkyl, phenyl or benzyl; R³¹ is a hydrogen atom, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋₆ haloalkyl, C₂₋₆ haloalkenyl, C₂₋₆ haloalkynyl, C₂₋₆ alkoxyalkyl, C₃₋₆ cycloalkyl, C₃₋ halocycloalkyl ₆, Cilt alkylthioalkyl, C₂₋₆ alkylsulfinyl alkyl, C₂₋₆ alkylsulfonylalkyl, C₂₋₆ alkylcarbonyl, C₂₋₆ haloalkylcarbonyl, C₂₋₆ alkoxycarbonyl, C₃₋₆ alkoxycarbonylalkyl, C₂₋₆-aminocarbonyl alkyl, (dialkylamino ) C₃₋₆ carbonyl, C₁₋₆-sulfonyl alkyl or C halo-sulfonyl haloalkyl; each of R⁷ and R⁸ is, independently, C alquilo alkyl, a halogen atom, C₃₋₆ cycloalkyl or C₁₋₄ haloalkyl; each of R⁹ and R¹⁰ is independently a hydrogen atom, a halogen atom, cyano, hydroxy, C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ alkynyl, C₁₋₆ haloalkyl, C₂₋₆ haloalkenyl , C₂₋₆ haloalkynyl, C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, C₃₋₆ cycloalkyl, C₁₋₆-thio alkyl, C₁₋₆-sulfinyl alkyl, C₁₋₆-sulfonyl alkyl, C₁₋₆-thio haloalkyl, haloalkyl C₁₋₆ sulfinyl or haloalkyl C₁₋₆-sulfonyl; and G¹ is an oxygen atom or a sulfur atom}, one of its enantiomers or one of its mixtures or an acceptable salt in agriculture or horticulture of said compound; and (b) at least one of an agricultural or horticultural fungicide or one of its salts. Claim 2: The fungicidal composition according to claim 1, characterized in that the compound of the formula (1) is selected from: 4- [4- (6-Methylsulfonyloxy-1,5-dihydro-3H-2,4-benzodioxepin -3-yl) -2-thiazolyl] -1- [2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] acetyl] piperidine, 4- [4- (6-fluoro-9 -methylsulfonyloxy-1,5-dihydro-3H-2,4-benzodioxepin-3-yl) -2-thiazolyl] -1- [2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl ] acetyl] piperidine, 4- [4- (6-methylsulfonyloxy-1,5-dihydro-3H-2,4-benzodioxepin-3-yl) -2-thiazolyl] -1- [2- [3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] acetyl] piperidine and @@@ 4- [4- (6-fluoro-9-methylsulfonyloxy-1,5-dihydro-3H-2,4-benzodioxepin-3-yl ) -2-thiazolyl] -1- [2- [3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] acetyl] piperidine, or mixtures thereof. Claim 3: The fungicidal composition according to claim 1 or 2, characterized in that component (b) comprises at least one compound selected from bentiavalicarb, valifenalate, zoxamide, famoxadone, iprovalicarb, fenamidone, fluopicolide, ametoctradine, ciazofamide, mandipropamide, methalaxyl -M, etaboxam, dimetomorf, cymoxanil, basic copper sulfate, chlorothalonyl, mancozeb, propineb, captane, kresoxim-methyl, azoxystrobin, trifloxystrobin, fluazinam, piribencarb, pentiopirad, quinoxifene, pyrophenone, propamocarbonaceous, propamocarbonaceous, propamocarbonaceous, propamocarbonate, aluminum thiophanate-methyl, iprodione, tebuconazole, cyprodinyl, amisulbrom, triciclazole, polyoxin, tebufloquine, propiconazole, oxathiapiproline or salts thereof. Claim 5: A method of controlling a plant pest, characterized in that it comprises a step of treating a plant or its vicinity with (a) the compound of the formula (1) according to claim 1 and (b) a fungicide agricultural or horticultural or one of its salts, where compounds (a) and (b) are applied for treatment simultaneously, sequentially or separately. |
| priorityDate | 2016-02-08-04:00^^<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: 113.