US2016219879A1PendingUtilityA1
Fungicidal compositions
Est. expiryDec 14, 2031(~5.4 yrs left)· nominal 20-yr term from priority
Inventors:Ulrich Johannes HaasDietrich HermannGabriel Didier ScallietKurt NebelLong LuQiang LuJianzhong YangThomas James HoffmanRenaud BeaudegniesWerner ZambachOlivier Jacob
C07D 409/12C07D 409/04C07D 407/12C07D 413/12C07D 417/12A01N 43/653C07D 213/74A01N 43/52A01N 55/00A01N 43/54A01N 35/06A01N 43/40C07F 7/0814A01N 37/38C07C 59/08A01N 53/00C07F 7/0812A01N 43/42A01N 37/34A01N 59/20C07D 405/12A01N 43/80A01N 43/56A01N 41/10A01N 57/20A01N 47/42A01N 43/82A01N 43/22A01N 43/38A01N 37/10A01N 43/36A01N 37/18Y02P60/21A01N 47/40A01N 43/84A01N 43/88A01N 59/16
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Claims
Abstract
The present invention provides a composition comprising a combination of components A) and B), wherein component A) is a compound of formula (I) and the component (B) is a further fungicide, insecticide or herbicide.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A compound of formula (I)
wherein
R 1 and R 2 are each independently selected from hydrogen and C 1 -C 4 alkyl;
or R 1 and R 2 together with the nitrogen atom to which they are connected form pyrrolidine or piperidine;
R 3 represents hydrogen, halogen, cyano, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, amino, C 1 -C 2 alkylamino, di(C 1 -C 6 alkyl)amino, pyrrolidino, imidazolino, triazolino, formyl, phenyl, C 2 -C 4 alkylcarbonyl, C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfinyl, C 1 -C 6 alkylsulfonyl or C 1 -C 6 hydroxyalkyl;
R 4 is selected from fluorine, chlorine, bromine, C 1 -C 4 alkyl, C 1 -C 4 alkenyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy and C 3 -C 6 cycloalkyl;
R 5 is selected from G 5 , G 6 -G 7 and G 10 -G 11 ;
G 5 is C 3 -C 7 cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH 3 )—CH 2 —CH 2 —CH 3 , —CH—CH(CH 3 )—CH 2 —CH 3 , —CH 2 —CH 2 —CH(CH 3 )—CH 3 , —CH 2 —CH 2 —CH(CH 3 ) 2 , —CH(CH 3 )—CH(CH 3 ) 2 , C 2 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 3 -C 4 -alkenyloxy, phenoxy and C 1 -C 6 alkylthio;
G 6 is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, CN, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 3 -C 6 alkenyloxy, C 3 -C 6 alkynyloxy and C 1 -C 6 alkylthio;
G 7 is methylene;
G 10 is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, OH, SH, CHO, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 3 -C 6 alkenyloxy, C 3 -C 6 alkynyloxy, C 3 -C 6 cycloalkoxy, phenyl, C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfinyl and C 1 -C 6 alkylsulfonyl.
G 11 is methylene substituted by at least one group independently selected from C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, CN, C 1 -C 4 alkoxy and C 1 -C 4 haloalkoxy;
R 6 is hydrogen;
R 7 is selected from hydrogen and C 1 -C 4 alkyl;
or an agronomically acceptable salt, metallic complex, metalloidic complex, isomer, structural isomer, stereo-isomer, diastereoisomer, enantiomer, tautomer, or N-oxide thereof.
2 . A compound of formula (I) according to claim 1 wherein R 1 and R 2 are each C 1 -C 4 alkyl;
R 3 represents hydrogen, halogen, cyano, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl or C 1 -C 4 alkylsulfonyl;
R 4 is selected from methyl, ethyl, methoxy, fluorine and chlorine;
R 6 is hydrogen;
R 7 is hydrogen or C 1 -C 4 alkyl.
3 . A compound of formula (I) according to claim 1 wherein R 1 and R 2 are each independently selected from methyl, ethyl and isopropyl;
R 3 represents hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, cyclopropyl, ethynyl or C 1 -C 4 alkoxy;
R 4 is selected from methyl, methoxy, fluorine and chlorine;
R 6 is hydrogen;
R 7 is hydrogen.
4 . A compound of formula (I) according to claim 1 wherein
R 1 is methyl;
R 2 is ethyl;
R 3 is selected from hydrogen, bromine, iodine, methyl, CHF 2 , cyclopropyl, ethynyl and methoxy;
R 4 is methyl;
R 6 is hydrogen;
R 7 is hydrogen.
5 . A compound of formula (I) according to claim 1 wherein R 5 is G 5 ; and
G 5 is C 6 cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH 3 )—CH 2 —CH 2 —CH 3 , —CH—CH(CH 3 )—CH 2 —CH 3 , —CH 2 —CH 2 —CH(CH 3 )—CH 3 , —CH 2 —CH 2 —CH(CH 3 ) 2 and —CH(CH 3 )—CH(CH 3 ) 2 .
6 . A compound according to claim 1 wherein R 5 is G 6 -G 7 ;
G 6 is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more halogen, CHF 2 , CF 3 and C 1 -C 4 alkyl; and
G 7 is methylene.
7 . A compound according to claim 1 wherein R 5 is G 10 -G 11 ;
G 10 is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, methyl, ethyl, n-propyl, iso-propyl, methoxy, CHF 2 , CF 3 and OCHF 2 and
G 11 is methylene substituted by at least one group independently selected from methyl, CF 3 and ethyl.
8 . A compound according to claim 1 wherein
R 1 is methyl;
R 2 is ethyl;
R 3 is selected from hydrogen, bromine, iodine, methyl, CHF 2 , cyclopropyl, ethynyl and methoxy;
R 4 is methyl;
R 5 is selected from G 5 , G 6 -G 7 and G 10 -G 11 ;
G 5 is C 6 cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH 3 )—CH 2 —CH 2 —CH 3 , —CH—CH(CH 3 )—CH 2 —CH 3 , —CH 2 —CH 2 —CH(CH 3 )—CH 3 , —CH 2 —CH 2 —CH(CH 3 ) 2 and —CH(CH 3 )—CH(CH 3 ) 2 ;
G 6 is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more halogen, CHF 2 , CF 3 and C 1 -C 4 alkyl;
G 7 is methylene;
G 10 is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, methyl, ethyl, n-propyl, iso-propyl, methoxy, CHF 2 , CF 3 and OCHF 2 ;
G 11 is methylene substituted by at least one group independently selected from methyl, CF 3 and ethyl;
R 6 is hydrogen; and
R 7 is hydrogen;
and agronomically acceptable salts/metallic complexes/metalloidic complexes/isomers/structural isomers/stereo-isomers/diastereoisomers/enantiomers/tautomers/N-oxides of those compounds.
9 . A fungicidal composition comprising a compound of formula (I) according to any one of claims 1 to 8 , an inert carrier and, optionally, an adjuvant.
10 . A fungicidal composition, comprising a combination of components A) and B), wherein component A) is a compound of formula (I) as defined in any of claims 1 to 8 , and agronomically acceptable salts/metallic complexes/metalloidic complexes/isomers/structural isomers/stereo-isomers/diastereoisomers/enantiomers/tautomers/N-oxides of those compounds, and component B) is a strobilurin fungicide, a sterol biosynthesis inhibitor, a triazole fungicide, a pro-triazole fungicide, a DMI fungicide, a SDHI fungicide, or a compound selected from the group consisting of Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid, Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin, Mefenoxam, Orocymedone, Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos, Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron, Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione, Tembotrione, Sulcotrione, Auxins, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese, Cyflufenamid, Tebufloquin and Copper.
11 . A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a compound of formula (I) according to any one of claims 1 to 8 or a fungicidal composition according to claim 9 or claim 10 .
12 . A method of protecting natural substances of plant origin, which have been taken from their natural life cycle, and/or their processed forms, which comprises applying to said natural substances of plant origin or their processed forms a compound of formula (I) according to any one of claims 1 to 8 or a fungicidal composition according to claim 9 or claim 10 .Join the waitlist — get patent alerts
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