Patent Application
20120108422
The present invention relates to novel triazole compounds of the formulae I and II as defined below which carry a sulfur substituent, to agricultural compositions containing them, to their use as fungicides and to intermediate compounds used in the method of producing them.
The control of plant diseases caused by phythopathogenic fungi is extremely important for achieving high crop efficiency. Plant disease damage to ornamental, vegetable, field, cereal, and fruit crops can cause significant reduction in productivity and thereby result in increased costs to the consumer.
DE 19528046, DE 19617461, DE 19617282, DE 19620407, DE 19620590, WO96/16048 and WO 97/43269 describe sulfurized triazolyl derivatives. The compounds are used for combating harmful fungi.
There is a continuous need for new compounds which are more effective, less costly, less toxic, environmentally safer and/or have different modes of action.
Accordingly, it is an object of the present invention to provide compounds having a better fungicidal activity and/or a better crop plant compatibility.
Surprisingly, these objects are achieved by triazole compounds of the general formulae I and II, defined below, and by the agriculturally acceptable salts of the compounds I and II.
Accordingly, the present invention relates to triazole compounds of the formulae I and II and to agriculturally useful salts thereof
wherein
The present invention also provides the use of triazole compounds of the formulae I and II and/or their agriculturally useful salts for controlling harmful fungi.
The invention further provides fungicidal compositions comprising these triazole compounds of the formulae I and/or II (and/or also of the formula IV; see below) and/or their agriculturally acceptable salts and suitable carriers. Suitable agriculturally acceptable carriers are described below.
The compounds I and II can exist as one or more stereoisomers. The various stereoisomers include enantiomers, diastereomers, atropisomers and geometric isomers. One skilled in the art will appreciate that one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate, enrich, and/or to selectively prepare said stereoisomers. The compounds of the invention may be present as a mixture of stereoisomers, e.g. a racemate, individual stereoisomers, or as an optically active form.
Compounds I and II can be understood as positional/double bond isomers of each other, at least in case the radicals R6/R6a are identical. In case R6 (and of course also R6a) is hydrogen, the respective compounds I and II are tautomers.
Suitable agriculturally useful salts are especially the salts of those cations or the acid addition salts of those acids whose cations and anions, respectively, have no adverse effect on the fungicidal action of the compounds I and II. Thus, suitable cations are in particular the ions of the alkali metals, preferably sodium and potassium, of the alkaline earth metals, preferably calcium, magnesium and barium, and of the transition metals, preferably manganese, copper, zinc and iron, and also the ammonium ion which, if desired, may carry one to four C1-C4-alkyl substituents and/or one phenyl or benzyl substituent, preferably diisopropylammonium, tetramethylammonium, tetrabutylammonium, trimethylbenzylammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(C1-C4-alkyl)sulfonium and sulfoxonium ions, preferably tri(C1-C4-alkyl)sulfoxonium.
Anions of useful acid addition salts are primarily chloride, bromide, fluoride, hydrogensulfate, sulfate, dihydrogenphosphate, hydrogenphosphate, phosphate, nitrate, bicarbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate, and also the anions of C1-C4-alkanoic acids, preferably formate, acetate, propionate and butyrate. They can be formed by reacting I or II with an acid of the corresponding anion, preferably hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid or nitric acid.
In the definitions of the variables given in the formulae above, collective terms are used which are generally representative for the substituents in question. The term Cn-Cm indicates the number of carbon atoms possible in each case in the substituent or substitutent moiety in question:
Halogen: fluorine, chlorine, bromine and iodine;
Alkyl and the alkyl moieties in alkoxy, alkoxyalkyl, alkoxyalkoxy, alkylcarbonyl, alkylthiocarbonyl, aminoalkyl, alkylamino, dialkylamino, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthio, alkylsulfonyl and the like: saturated straight-chain or branched hydrocarbon radicals having 1 to 2 (C1-C2-alkyl), 2 or 3 (C2-C3-alkyl), 1 to 4 (C1-C4-alkyl), 1 to 6 (C1-C6-alkyl), 1 to 8 (C1-C8-alkyl) or 1 to 10 (C1-C10-alkyl) carbon atoms. C2-C3-Alkyl is ethyl, n-propyl or isopropyl. C1-C2-Alkyl is methyl or ethyl. C1-C4-Alkyl is methyl, ethyl, propyl, isopropyl, butyl, 1-methylpropyl (sec-butyl), 2-methylpropyl (isobutyl) or 1,1-dimethylethyl (tert-butyl). C1-C6-Alkyl is additionally also, for example, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl, or 1-ethyl-2-methylpropyl. C1-C8-Alkyl is additionally also, for example, heptyl, octyl, 2-ethylhexyl and positional isomers thereof. C1-C10-Alkyl is additionally also, for example, nonyl, decyl, 2-propylheptyl, 3-propylheptyl and positional isomers thereof.
Haloalkyl: straight-chain or branched alkyl groups having 1 to 2 (C1-C2-haloalkyl), 1 to 3 (C1-C3-haloalkyl), 1 to 4 (C1-C4-haloalkyl), 1 to 6 (C1-C6-haloalkyl), 1 to 8 (C1-C8-haloalkyl), 1 to 10 (C1-C10-haloalkyl) or 2 to 10 (C2-C10-haloalkyl) carbon atoms (as mentioned above), where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above: in particular C1-C2-haloalkyl, such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, or pentafluoroethyl. C1-C3-Haloalkyl is additionally, for example, 1,1,1-trifluoroprop-2-yl, 3,3,3-trifluoropropyl or heptafluoropropyl. C1-C4-Haloalkyl is additionally, for example, 1-chlorobutyl, 2-chlorobutyl, 3-chlorobutyl or 4-chlorobutyl.
C1-C10-Hydroxyalkyl: straight-chain or branched alkyl groups having 1 to 2 (C1-C2-hydroxyalkyl), 1 to 4 (C1-C4-hydroxyalkyl), 2 to 4 (C2-C4-hydroxyalkyl), 1 to 6 (C1-C6-hydroxyalkyl), 2 to 6 (C2-C6-hydroxyalkyl), 1 to 8 (C1-C8-hydroxyalkyl), 2 to 8 (C2-C8-hydroxyalkyl), 1 to 10 (C1-C10-hydroxyalkyl) or 2 to 10 (C2-C10-hydroxyalkyl) carbon atoms (as mentioned above), where at least one of the hydrogen atoms is replaced by a hydroxyl group, such as in 2-hydroxyethyl or 3-hydroxypropyl.
Alkenyl and the alkenyl moieties in alkenyloxy, alkenylthio, alkenylcarbonyl and the like: monounsaturated straight-chain or branched hydrocarbon radicals having 2 to 4 (C2-C4-alkenyl), 2 to 6 (C2-C6-alkenyl), 2 to 8 (C2-C8-alkenyl), 3 to 8 (C3-C8-alkenyl), 2 to 10 (C2-C10-alkenyl) or 3 to 10 (C3-C10-alkenyl) carbon atoms and a double bond in any position, for example C2-C4-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl or 2-methyl-2-propenyl, or, for example, C2-C6-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl, 1-ethyl-2-methyl-2-propenyl and the like;
Haloalkenyl and the haloalkenyl moieties in haloalkenyloxy, haloalkenylcarbonyl and the like: unsaturated straight-chain or branched hydrocarbon radicals having 2 to 4 (C2-C4-haloalkenyl), 2 to 6 (C2-C6-haloalkenyl), 2 to 8 (C2-C8-haloalkenyl) or 2 to 10 (C2-C10-haloalkenyl) carbon atoms and a double bond in any position (as mentioned above), where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, in particular fluorine, chlorine and bromine, for example chlorovinyl, chloroallyl and the like;
Alkynyl and the alkynyl moieties in alkynyloxy, alkynylthio, alkynylcarbonyl and the like: straight-chain or branched hydrocarbon groups having 2 to 4 (C2-C4-alkynyl), 2 to 6 (C2-C6-alkynyl), 2 to 8 (C2-C8-alkynyl), 3 to 8 (C3-C8-alkynyl), 2 to 10 (C2-C10-alkynyl) or 3 to 10 (C3-C10-alkynyl) carbon atoms and one or two triple bonds in any position, for example C2-C4-alkynyl, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, or 1-methyl-2-propynyl, or, for example, C2-C6-alkynyl, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl, 1-ethyl-1-methyl-2-propynyl and the like;
Haloalkynyl and the haloalkynyl moieties in haloalkynyloxy, haloalkynylcarbonyl and the like: unsaturated straight-chain or branched hydrocarbon radicals having 2 to 4 (C2-C4-haloalkynyl), 2 to 6 (C2-C6-haloalkynyl), 2 to 8 (C2-C8-haloalkynyl) or 2 to 10 (C2-C10-haloalkynyl) carbon atoms and one or two triple bonds in any position (as mentioned above), where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, in particular fluorine, chlorine and bromine; Cycloalkyl and the cycloalkyl moieties in cycloalkoxy, cycloalkylcarbonyl and the like; monocyclic saturated hydrocarbon groups having 3 to 6 (C3-C6-cycloalkyl), 3 to 8 (C3-C8-cycloalkyl) or 3 to 10 (C3-C10-cycloalkyl) carbon ring members, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl and cyclodecyl;
Halocycloalkyl and the halocycloalkyl moieties in halocycloalkoxy, halocycloalkylcarbonyl and the like: monocyclic saturated hydrocarbon groups having 3 to 6 (C3-C6-halocycloalkyl), 3 to 8 (C3-C8-halocycloalkyl) or 3 to 10 (C3-C10-halocycloalkyl) carbon ring members (as mentioned above) in which some or all of the hydrogen atoms may be replaced by halogen atoms as mentioned above, in particular fluorine, chlorine and bromine;
Cycloalkenyl and the cycloalkenyl moieties in cycloalkenyloxy, cycloalkenylcarbonyl and the like; monocyclic monounsaturated hydrocarbon groups having 3 to 6 (C3-C6-cycloalkenyl), 3 to 8 (C3-C8-cycloalkenyl) or 3 to 10 (C3-C10-cycloalkenyl) carbon ring members, such as cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, cyclononenyl and cyclodecenyl;
Halocycloalkenyl and the halocycloalkenyl moieties in halocycloalkenyloxy, halocycloalkenylcarbonyl and the like: monocyclic monounsaturated hydrocarbon groups having 3 to 6 (C3-C6-halocycloalkenyl), 3 to 8 (C3-C8-halocycloalkenyl) or 3 to 10 (C3-C10-halocycloalkenyl) carbon ring members (as mentioned above) in which some or all of the hydrogen atoms may be replaced by halogen atoms as mentioned above, in particular fluorine, chlorine and bromine;
C3-C6-cycloalkyl-C1-C2-alkyl: a C1-C2-alkyl residue, as described above, wherein one of the hydrogen atoms is replaced by a C3-C6-cycloalkyl group. Examples are cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, cyclopropyl-1-ethyl, cyclobutyl-1-ethyl, cyclopentyl-1-ethyl, cyclohexyl-1-ethyl, cyclopropyl-2-ethyl, cyclobutyl-2-ethyl, cyclopentyl-2-ethyl, cyclohexyl-2-ethyl and the like. C3-C10-cycloalkyl-C1-C4-alkyl is a C1-C4-alkyl residue, as described above, wherein one of the hydrogen atoms is replaced by a C3-C10-cycloalkyl group. Examples are, apart those mentioned above for C3-C6-cycloalkyl-C1-C4-alkyl, cycloheptylmethyl, cyclooctylmethyl, cyclononylmethyl, cyclodecylmethyl, cycloheptyl-1-ethyl, cyclooctyl-1-ethyl, cyclononyl-1-ethyl, cyclodecyl-1-ethyl, cycloheptyl-2-ethyl, cyclooctyl-2-ethyl, cyclononyl-2-ethyl, cyclodecyl-2-ethyl, cyclopropyl-1-propyl, cyclopropyl-2-propyl, cyclopropyl-3-propyl, cyclobutyl-1-propyl, cyclobutyl-2-propyl, cyclobutyl-3-propyl, cyclopentyl-1-propyl, cyclopentyl-2-propyl, cyclopentyl-3-propyl, cyclohexyl-1-propyl, cyclohexyl-2-propyl, cyclohexyl-3-propyl, cycloheptyl-1-propyl, cycloheptyl-2-propyl, cycloheptyl-3-propyl, cyclooctyl-1-propyl, cyclooctyl-2-propyl, cyclooctyl-3-propyl, cyclononyl-1-propyl, cyclononyl-2-propyl, cyclononyl-3-propyl, cyclodecyl-1-propyl, cyclodecyl-2-propyl, cyclodecyl-3-propy, cyclopropyl-1-butyl, cyclopropyl-2-butyl, cyclopropyl-3-butyl, cyclopropyl-4-butyl, cyclobutyl-1-butyl, cyclobutyl-2-butyl, cyclobutyl-3-butyl, cyclobutyl-4-butyl, cyclopentyl-1-butyl, cyclopentyl-2-butyl, cyclopentyl-3-butyl, cyclopentyl-4-butyl, cyclohexyl-1-butyl, cyclohexyl-2-butyl, cyclohexyl-3-butyl, cyclohexyl-4-butyl, cycloheptyl-1-butyl, cycloheptyl-2-butyl, cycloheptyl-3-butyl, cycloheptyl-4-butyl, cyclooctyl-1-butyl, cyclooctyl-2-butyl, cyclooctyl-3-butyl, cyclooctyl-4-butyl, cyclononyl-1-butyl, cyclononyl-2-butyl, cyclononyl-3-butyl, cyclononyl-4-butyl, cyclodecyl-1-butyl, cyclodecyl-2-butyl, cyclodecyl-3-butyl, cyclodecyl-4-butyl, and the like.
C3-C6-halocycloalkyl-C1-C2-alkyl: a C1-C2-alkyl residue, as described above, wherein one of the hydrogen atoms is replaced by a C3-C6-halocycloalkyl group. Examples are 1-chlorocyclopropylmethyl, 1-chlorocyclobutylmethyl, 1-chlorocyclopentylmethyl, 1-chlorocyclohexylmethyl, 1-chlorocyclopropyl-1-ethyl, 1-chlorocyclobutyl-1-ethyl, 1-chlorocyclopentyl-1-ethyl, 1-chlorocyclohexyl-1-ethyl, 1-chlorocyclopropyl-2-ethyl, 1-chlorocyclobutyl-2-ethyl, 1-chlorocyclopentyl-2-ethyl, 1-chlorocyclohexyl-2-ethyl, 2-chlorocyclopropylmethyl, 2-chlorocyclobutylmethyl, 2-chlorocyclopentylmethyl, 2-chlorocyclohexylmethyl, 2-chlorocyclopropyl-1-ethyl, 2-chlorocyclobutyl-1-ethyl, 2-chlorocyclopentyl-1-ethyl, 2-chlorocyclohexyl-1-ethyl, 2-chlorocyclopropyl-2-ethyl, 2-chlorocyclobutyl-2-ethyl, 2-chlorocyclopentyl-2-ethyl, 2-chlorocyclohexyl-2-ethyl, 1-fluorocyclopropylmethyl, 1-fluorocyclobutylmethyl, 1-fluorocyclopentylmethyl, 1-fluorocyclohexylmethyl, 1-fluorocyclopropyl-1-ethyl, 1-fluorocyclobutyl-1-ethyl, 1-fluorocyclopentyl-1-ethyl, 1-fluorocyclohexyl-1-ethyl, 1-fluorocyclopropyl-2-ethyl, 1-fluorocyclobutyl-2-ethyl, 1-fluorocyclopentyl-2-ethyl, 1-fluorocyclohexyl-2-ethyl, 2-fluorocyclopropylmethyl, 2-fluorocyclobutylmethyl, 2-fluorocyclopentylmethyl, 2-fluorocyclohexylmethyl, 2-fluorocyclopropyl-1-ethyl, 2-fluorocyclobutyl-1-ethyl, 2-fluorocyclopentyl-1-ethyl, 2-fluorocyclohexyl-1-ethyl, 2-fluorocyclopropyl-2-ethyl, 2-fluorocyclobutyl-2-ethyl, 2-fluorocyclopentyl-2-ethyl, 2-fluorocyclohexyl-2-ethyl, and the like. C3-C10-halocycloalkyl-C1-C4-alkyl is a C1-C4-alkyl residue, as described above, wherein one of the hydrogen atoms is replaced by a C3-C10-halocycloalkyl group.
Alkoxy: an alkyl group attached via oxygen. C1-C2-Alkoxy is methoxy or ethoxy. C1-C3-Alkoxy is additionally, for example, n-propoxy or 1-methylethoxy (isopropoxy). Alkoxy is additionally, for example, butoxy, 1-methylpropoxy (sec-butoxy), 2-methylpropoxy (isobutoxy) or 1,1-dimethylethoxy (tert-butoxy). C1-C6-Alkoxy is additionally, for example, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy or 1-ethyl-2-methylpropoxy. C1-C8-Alkoxy is additionally, for example, heptyloxy, octyloxy, 2-ethylhexyloxy and positional isomers thereof. C1-C10-Alkoxy is additionally, for example, nonyloxy, decyloxy and positional isomers thereof. C2-C10-Alkoxy is like C1-C10-alkoxy with the exception of methoxy.
Haloalkoxy: an alkoxy radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, preferably by fluorine. C1-C2-Haloalkoxy is, for example, OCH2F, OCHF2, OCF3, OCH2Cl, OCHCl2, OCCl3, chlorofluoromethoxy, dichlorofluoromethoxy, chlorodifluoromethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy or OC2F5. C1-C4-Haloalkoxy is additionally, for example, 2-fluoropropoxy, 3-fluoropropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy, 2-chloropropoxy, 3-chloropropoxy, 2,3-dichloropropoxy, 2-bromopropoxy, 3-bromopropoxy, 3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy, OCH2—C2F5, OCF2—C2F5, 1-(CH2F)-2-fluoroethoxy, 1-(CH2Cl)-2-chloroethoxy, 1-(CH2Br)-2-bromoethoxy, 4-fluorobutoxy, 4-chlorobutoxy, 4-bromobutoxy or nonafluorobutoxy. C1-C6-Haloalkoxy is additionally, for example, 5-fluoropentoxy, 5-chloropentoxy, 5-brompentoxy, 5-iodopentoxy, undecafluoropentoxy, 6-fluorohexoxy, 6-chlorohexoxy, 6-bromohexoxy, 6-iodohexoxy or dodecafluorohexoxy.
Alkenyloxy: alkenyl as mentioned above which is attached via an oxygen atom, for example C2-C10-alkenyloxy, such as 1-ethenyloxy, 1-propenyloxy, 2-propenyloxy, 1-methylethenyloxy, 1-butenyloxy, 2-butenyloxy, 3-butenyloxy, 1-methyl-1-propenyloxy, 2-methyl-1-propenyloxy, 1-methyl-2-propenyloxy, 2-methyl-2-propenyloxy, 1-pentenyloxy, 2-pentenyloxy, 3-pentenyloxy, 4-pentenyloxy, 1-methyl-1-butenyloxy, 2-methyl-1-butenyloxy, 3-methyl-1-butenyloxy, 1-methyl-2-butenyloxy, 2-methyl-2-butenyloxy, 3-methyl-2-butenyloxy, 1-methyl-3-butenyloxy, 2-methyl-3-butenyloxy, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyloxy, 1,2-dimethyl-1-propenyloxy, 1,2-dimethyl-2-propenyloxy, 1-ethyl-1-propenyloxy, 1-ethyl-2-propenyloxy, 1-hexenyloxy, 2-hexenyloxy, 3-hexenyloxy, 4-hexenyloxy, 5-hexenyloxy, 1-methyl-1-pentenyloxy, 2-methyl-1-pentenyloxy, 3-methyl-1-pentenyloxy, 4-methyl-1-pentenyloxy, 1-methyl-2-pentenyloxy, 2-methyl-2-pentenyloxy, 3-methyl-2-pentenyloxy, 4-methyl-2-pentenyloxy, 1-methyl-3-pentenyloxy, 2-methyl-3-pentenyloxy, 3-methyl-3-pentenyloxy, 4-methyl-3-pentenyloxy, 1-methyl-4-pentenyloxy, 2-methyl-4-pentenyloxy, 3-methyl-4-pentenyloxy, 4-methyl-4-pentenyloxy, 1,1-dimethyl-2-butenyloxy, 1,1-dimethyl-3-butenyloxy, 1,2-dimethyl-1-butenyloxy, 1,2-dimethyl-2-butenyloxy, 1,2-dimethyl-3-butenyloxy, 1,3-dimethyl-1-butenyloxy, 1,3-dimethyl-2-butenyloxy, 1,3-dimethyl-3-butenyloxy, 2,2-dimethyl-3-butenyloxy, 2,3-dimethyl-1-butenyloxy, 2,3-dimethyl-2-butenyloxy, 2,3-dimethyl-3-butenyloxy, 3,3-dimethyl-1-butenyloxy, 3,3-dimethyl-2-butenyloxy, 1-ethyl-1-butenyloxy, 1-ethyl-2-butenyloxy, 1-ethyl-3-butenyloxy, 2-ethyl-1-butenyloxy, 2-ethyl-2-butenyloxy, 2-ethyl-3-butenyloxy, 1,1,2-trimethyl-2-propenyloxy, 1-ethyl-1-methyl-2-propenyloxy, 1-ethyl-2-methyl-1-propenyloxy and 1-ethyl-2-methyl-2-propenyloxy and the like;
Haloalkenyloxy: an alkenyloxy radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, preferably by fluorine.
Alkynyloxy: alkynyl as mentioned above which is attached via an oxygen atom, for example C2-C10-alkynyloxy, such as 2-propynyloxy, 2-butynyloxy, 3-butynyloxy, 1-methyl-2-propynyloxy, 2-pentynyloxy, 3-pentynyloxy, 4-pentynyloxy, 1-methyl-2-butynyloxy, 1-methyl-3-butynyloxy, 2-methyl-3-butynyloxy, 1-ethyl-2-propynyloxy, 2-hexynyloxy, 3-hexynyloxy, 4-hexynyloxy, 5-hexynyloxy, 1-methyl-2-pentynyloxy, 1-methyl-3-pentynyloxy and the like;
Haloalkynyloxy: an alkynyloxy radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, preferably by fluorine.
Cycloalkoxy: cycloalkyl as mentioned above which is attached via an oxygen atom, for example C3-C10-cycloalkoxy or C3-C8-cycloalkoxy, such as cyclopropoxy, cyclopentoxy, cyclohexoxy, cycloheptoxy, cyclooctoxy, cyclononyloxy, cyclodecyloxy and the like;
Cycloalkenyloxy: cycloalkenyl as mentioned above which is attached via an oxygen atom, for example C3-C10-cycloalkenyloxy, C3-C8-cycloalkenyloxy or, preferably, C5-C6-cycloalkenyloxy, such as cyclopent-1-enoxy, cyclopent-2-enoxy, cyclohex-1-enoxy and cyclohex-2-enoxy;
Alkoxyalkyl: alkyl as defined above having 1 to 10, 1 to 8, 1 to 6 or 1 to 4, in particular 1 to 3, carbon atoms, in which one hydrogen atom is replaced by an alkoxy group having 1 to 8, 1 to 6, 1 to 4 or 1 to 3 carbon atoms, for example methoxymethyl, 2-methoxyethyl, ethoxymethyl, 3-methoxypropyl, 3-ethoxypropyl and the like.
Alkoxyalkoxy: alkoxy as defined above having 1 to 10, 1 to 8, 1 to 6 or 1 to 4, in particular 1 to 3, carbon atoms, in which one hydrogen atom is replaced by an alkoxy group having 1 to 8, 1 to 6 or in particular 1 to 4 carbon atoms, for example 2-methoxyethoxy, 2-ethoxyethoxy, 3-methoxypropoxy, 3-ethoxypropoxy and the like.
Alkylcarbonyl: group of the formula R—CO— in which R is an alkyl group as defined above, for example C1-C10-alkyl, C1-C8-alkyl, C1-C6-alkyl, C1-C4-alkyl, C1-C2-alkyl or C3-C4-alkyl. Examples are acetyl, propionyl and the like. Examples for C3-C4-alkylcarbonyl are propylcarbonyl, isopropylcarbonyl, n-butylcarbonyl, sec-butylcarbonyl, isobutylcarbonyl and tert-butylcarbonyl.
Haloalkylcarbonyl: group of the formula R—CO— in which R is a haloalkyl group as defined above, for example C1-C10-haloalkyl, C1-C8-haloalkyl, C1-C6-haloalkyl, C1-C4-haloalkyl, C1-C2-haloalkyl or C3-C4-haloalkyl. Examples are difluoromethylcarbonyl, trifluoromethylcarbonyl, 2,2-difluoroethylcarbony, 2,2,3-trifluoroethylcarbonyl and the like.
Alkoxycarbonyl: group of the formula R—CO— in which R is an alkoxy group as defined above, for example C1-C10-alkoxy, C1-C8-alkoxy, C1-C6-alkoxy, C1-C4-alkoxy or C1-C2-alkoxy. Examples for C1-C4-alkoxycarbonyl are methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, sec-butoxycarbonyl, isobutoxycarbonyl and tert-butoxycarbonyl.
Haloalkoxycarbonyl: group of the formula R—CO— in which R is a haloalkoxy group as defined above, for example C1-C10-haloalkoxy, C1-C8-haloalkoxy, C1-C6-haloalkoxy, C1-C4-haloalkoxy or C1-C2-haloalkoxy. Examples for C1-C4-haloalkoxycarbonyl are difluoromethoxycarbonyl, trifluoromethoxycarbonyl, 2,2-difluoroethoxycarbony, 2,2,3-trifluoroethoxycarbonyl and the like.
Alkylaminocarbonyl: group of the formula R—NH—CO— in which R is an alkyl group as defined above, for example C1-C10-alkyl, C1-C8-alkyl, C1-C6-alkyl, C1-C4-alkyl, C1-C2-alkyl or C3-C4-alkyl. Examples for C1-C4-alkylaminocarbonyl are methylaminocarbonyl, ethylaminocarbonyl, propylaminocarbonyl, isopropylaminocarbonyl, butylaminocarbonyl, sec-butylaminocarbonyl, isobutylaminocarbonyl and tert-butylaminocarbonyl.
Dialkylaminocarbonyl: group of the formula RR′N—CO— in which R and R′, independently of each other, are an alkyl group as defined above, for example C1-C10-alkyl, C1-C8-alkyl, C1-C6-alkyl, C1-C4-alkyl, C1-C2-alkyl or C3-C4-alkyl. Examples for di-(C1-C4-alkyl)aminocarbonyl are dimethylaminocarbonyl, diethylaminocarbonyl, dipropylaminocarbonyl, diisopropylaminocarbonyl and dibutylaminocarbonyl.
Aminoalkyl: group of the formula R—NH2 in which R is an alkyl group as defined above, for example C1-C10-alkyl, C1-C2-alkyl or C3-C4-alkyl. Examples are aminomethyl, 1- and 2-aminoethyl, 1-, 2- and 3-aminopropyl, 1- and 2-amino1-methylethyl, 1-, 2-, 3- and 4-aminobutyl and the like.
Alkylsulfonyl: group of the formula R—S(O)2— in which R is an alkyl group as defined above, for example C1-C10-alkyl, C1-C4-alkyl or C1-C2-alkyl. Examples for C1-C4-alkylsulfonyl are methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, sec-butylsulfonyl, isobutylsulfonyl and tert-butylsulfonyl.
Alkylthio: alkyl as defined above which is attached via a sulfur atom.
Haloalkylthio: haloalkyl as defined above which is attached via a sulfur atom.
Alkenylthio: alkenyl as defined above which is attached via a sulfur atom.
Haloalkenylthio: haloalkenyl as defined above which is attached via a sulfur atom.
Alkynylthio: alkynyl as defined above which is attached via a sulfur atom.
Haloalkynylthio: haloalkynyl as defined above which is attached via a sulfur atom.
Cycloalkylthio: cycloalkyl as defined above which is attached via a sulfur atom.
Aryl is a carbocyclic aromatic monocyclic or polycyclic ring containing 6 to 16 carbon atoms as ring members. Examples are phenyl, naphthyl, anthracenyl, phenanthrenyl, fluorenyl and azulenyl. Preferably, aryl is phenyl or naphthyl, and especially phenyl.
Phenyl-C1-C4-alkyl: C1-C4-alkyl (as defined above), where a hydrogen atom is replaced by a phenyl group, such as benzyl, phenethyl and the like.
Phenyl-C1-C4-alkoxy: C1-C4-alkoxy (as defined above), where one hydrogen atom is replaced by a phenyl group, such as benzyloxy, phenethyloxy and the like.
3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated or maximum unsaturated carbocyclic radical: cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclobutadienyl, cyclopentadienyl, cyclohexadienyl, cycloheptadienyl or cycloheptatrienyl. Formally, phenyl is also included in this definition, but as it is also encompassed in the term aryl, it is not listed here.
3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated or maximum unsaturated heterocycle which contains 1, 2 or 3 heteroatoms or heteroatom containing groups selected from oxygen, nitrogen (as N or NR) and sulfur (as S, SO or SO2) and optionally 1 or 2 groups selected from C(═O) and C(═S) as ring members:
C2-C5-Alkylene: divalent branched or preferably unbranched chains having 2 to 5 carbon atoms, for example CH2CH2, —CH(CH3)—, CH2CH2CH2, CH(CH3)CH2, CH2CH(CH3), CH2CH2CH2CH2, CH2CH2CH2CH2CH2.
C4-C5-Alkylene: divalent branched or preferably unbranched chains having 4 to 5 carbon atoms, for example CH2CH2CH2CH2 or CH2CH2CH2CH2CH2.
The group —SM is more correctly spoken a group —S−M+, where M+ is a metal cation equivalent or an ammonium cation as defined above. A metal cation equivalent is more correctly spoken 1/a Ma+, where a is the valence of the metal and is in general 1, 2 or 3.
The protective group in the definition of R2 may be any oxygen-protective group (to be more precise: an OH protective group) known in the art. OH groups, for instance, can be protected by means of a benzyl group, introduced by reaction with benzyl chloride for example; by a silyl protective group, for example trimethylsilyl (TMS), tert-butyldimethylsilyl (TBDMS) or tert-butyldiphenylsilyl (TBDPS), which is introduced by reaction with the corresponding chloride; by the tetrahydropyranyl protective group; by an alkyl group, such as C1-C6-alkyl; by a haloalkyl group, such as C1-C4-haloalkyl; by an alkenyl group, such as C2-C6-alkenyl; by a haloalkenyl group, such as C2-C4-haloalkenyl; by an alkylcarbonyl group, such as C1-C4-alkylcarbonyl; by a haloalkylcarbonyl group, such as C1-C4-haloalkylcarbonyl; by an alkoxycarbonyl protective group, such as C1-C4-alkoxycarbonyl; by a haloalkoxycarbonyl protective group, such as 2,2,2-trichloroethoxycarbonyl (TROC); or by an alkyl- or dialkylaminocarbonyl protective group, such as C1-C4alkylaminocarbonyl or di-(C1-C4alkyl)-aminocarbonyl.
The statements made below with respect to suitable and preferred features of the compounds according to the invention, especially with respect to their substituents R1, R2; R3; R4, R5; R6; R6a, R7; R8, R9; R10, R11, R12, R13, R14, R15, R16, R17, Ra; Rb; Rc; Rd; Q, M and the indices m and n, and to their use, are valid both per se and, in particular, in every possible combination with one another.
n is preferably 3, 4 or 5 and is specifically 3.
R1 is preferably selected from C1-C6-alkyl, C1-C4-haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C3-C6-cycloalkyl-C1-C2-alkyl, C3-C6-halocycloalkyl-C1-C2-alkyl, where the cycloalkyl moiety in the 4 last-mentioned radicals may carry 1 or 2 substituents R8, where R8 is preferably selected from methyl, difluoromethyl and trifluoromethyl; phenyl which may carry 1, 2, 3, 4 or 5, preferably 1, 2 or 3 and in particular 1 or 2, substituents R7, and a 5- or 6-membered heteroaromatic ring containing 1, 2 or 3 heteroatoms selected from N, O and S as ring members, where the heteroaromatc ring may carry 1, 2 or 3 substituents R7. More preferably, R1 is selected from C1-C6-alkyl, C1-C4haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C3-C6-cycloalkyl-C1-C2-alkyl, C3-C6-halocycloalkyl-C1-C2-alkyl, where the cycloalkyl moiety in the 4 last-mentioned radicals may carry 1 substituent R8 selected from methyl, difluoromethyl and trifluoromethyl, and phenyl which may carry 1, 2, 3, 4 or 5, preferably 1, 2 or 3 and in particular 1 or 2, substituents R7.
Even more preferably, R1 is selected from C1-C4alkyl (preferably C1-C4alkyl), cyclopropyl, 1-methylcyclopropyl, 1-chlorocyclopropyl, 1-cyclopropylethyl and phenyl which may carry 1, 2, 3, 4 or 5, preferably 1, 2 or 3 and in particular 1 or 2, substituents and particularly preferably from tert-butyl, cyclopropyl, 1-methylcyclopropyl, 1-chlorocyclopropyl, 1-cyclopropylethyl and phenyl. Specifically, R1 is tert-butyl.
The protective group in the definition of R2 is preferably selected from benzyl, a silyl protective group, such as trimethylsilyl (TMS), tert-butyldimethylsilyl (TBDMS) or tert-butyldiphenylsilyl (TBDPS), C1-C6-alkyl, C1-C4-haloalkyl, C2-C6-alkenyl, C2-C4-haloalkenyl, C1-C4-alkylcarbonyl, C1-C4-haloalkylcarbonyl, C1-C4-alkoxycarbonyl, C1-C4-haloalkoxycarbonyl, C1-C4-alkylaminocarbonyl, and di-(C1-C4alkyl)-aminocarbonyl. More preferably, the protective group in the definition of R2 is selected from C1-C6-alkyl, C1-C4haloalkyl, C2-C6-alkenyl, C2-C4-haloalkenyl, C1-C4alkylcarbonyl, haloalkylcarbonyl, C1-C4-alkoxycarbonyl, C1-C4-haloalkoxycarbonyl, C1-C4-alkylaminocarbonyl, and di-(C1-C4-alkyl)-aminocarbonyl.
R2 is preferably selected from hydrogen and the above listed preferred and more preferred protective groups. More preferably, R2 is hydrogen.
R3 and R4, independently of each other and independently of each occurrence, are preferably selected from hydrogen, halogen and C1-C4-alkyl and more preferably from hydrogen, F, Cl, methyl and ethyl. Even more preferably, one of the radicals R3 and R4 is selected from hydrogen, F, Cl, methyl and ethyl and the remaining radicals R3 and R4 are all hydrogen. Particularly preferably, one of the radicals R3 and R4 is methyl and the remaining radicals R3 and R4 are all hydrogen or all radicals R3 and R4 are hydrogen.
R5 is preferably selected from phenyl which may carry 1, 2 or 3 substituents R9, and a 5- or 6-membered heteroaromatic ring containing 1, 2 or 3 heteroatoms selected from N, O and S as ring members, where the heteroaromatic ring may carry 1, 2 or 3 substituents R10.
More preferably, R5 is phenyl which may carry 1, 2 or 3, preferably 1 or 2 substituents R9.
R9 is preferably selected from halogen, methyl, difluoromethyl, trifluoromethyl, methoxy, difluoromethoxy and trifluoromethoxy and preferably from halogen. Halogen is in this case preferably selected from fluorine, chlorine and bromine and more preferably from fluorine and chlorine.
Alternatively preferably, especially when R5 is phenyl, R9 is fluorine. More preferably in this case, R5 is phenyl which carries one fluorine substituent. More preferred groups R9 are thus 2-fluorophenyl, 3-fluorophenyl and 4-fluorophenyl.
In another alternatively preferred embodiment, R5 is phenyl which may carry 1, 2 or 3 substituents R9 selected from nitro, CN, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and NR15R16. More preferably, R5 is phenyl which may carry 1, 2 or 3 substituents R9 selected from C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy. Even more preferably, R5 is phenyl which may carry 1, 2 or 3 substituents R9 selected from methyl and trifluoromethyl. Examples therefore are 2,3-dimethylphenyl, 2,4-dimethylphenyl, 2,5-dimethylphenyl, 2,6-dimethylphenyl, 3,4-dimethylphenyl, 3,5-dimethylphenyl, 2,3-di(trifluoromethyl)phenyl, 2,4-di(trifluoromethyl)phenyl, 2,5-di(trifluoromethyl)phenyl, 2,6-di(trifluoromethyl)phenyl, 3,4-di(trifluoromethyl)phenyl and 2,6-di(trifluoromethyl)phenyl.
In yet another alternatively preferred embodiment, R5 is phenyl which carries 2 or 3 substituents selected from halogen, nitro, CN, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and NR15R16. In this case it is preferred that at least one of the 2 or 3 substituents is fluorine. Preferably, the second and, if present, the third substituent are selected from halogen, especially fluorine and chlorine, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy, more preferably from halogen, especially fluorine and chlorine, C1-C4-alkyl and C1-C4-haloalkyl, and in particular from fluorine, chlorine, methyl and trifluoromethyl. Examples for such radicals R5 are 2,3-difluorophenyl, 2,4-difluorophenyl, 2,5-difluorophenyl, 2,6-difluorophenyl, 3,4-difluorophenyl, 3,5-difluorophenyl, 2,3,4-trifluorophenyl, 2,4,6-trifluorophenyl, 3,4,5-trifluorophenyl, 2-chloro-3-difluorophenyl, 2-chloro-4-difluorophenyl, 2-chloro-5-difluorophenyl, 2-chloro-6-difluorophenyl, 3-chloro-4-difluorophenyl, 3-chloro-5-difluorophenyl, 3-chloro-2-difluorophenyl, 4-chloro-2-difluorophenyl, 5-chloro-2-difluorophenyl, 4-chloro-3-difluorophenyl, 2,4-dichloro-3-fluoro, 2,4-dichloro-5-fluoro, 2,4-dichloro-6-fluoro, 2,6-dichloro-3-fluoro, 2,6-dichloro-6-fluoro, 4-chloro-2,3-difluoro, 4-chloro-2,5-difluoro, 4-chloro-2,6-difluoro, 3-chloro-2,4-difluoro, 3-chloro-2,5-difluoro, 4-chloro-2,6-difluoro, and the like.
In yet another alternatively preferred embodiment, R5 is phenyl which carries 1 or 2 substituents selected from 2-Cl, 3-Cl, 2,3-Cl2, 2,4-Cl2, 2,5-Cl2, 3,4-Cl2 and 3,5-Cl2, relative to the 1-position of the attachment point of the phenyl ring to the remainder of the molecule.
Preferably, R7, R10 and R11 are independently of each other and independently of each occurrence selected from halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy and more preferably from methyl, difluoromethyl, trifluoromethyl, methoxy, difluoromethoxy and trifluoromethoxy.
Preferably, R8 is independently of each occurrence selected from C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and C1-C4-haloalkoxy and more preferably from methyl, difluoromethyl, trifluoromethyl, methoxy, difluoromethoxy and trifluoromethoxy.
R12 in the groups —C(═O)R12 and —S(O)2R12 is preferably selected from C1-C4-alkyl, C1-C2-haloalkyl, C1-C4-alkoxy, C1-C2-haloalkoxy, phenyl, phenoxy and NR15R16, more preferably from C1-C4-alkyl, C1-C2-haloalkyl, C1-C4-alkoxy, C1-C2-haloalkoxy and NR15R16 and even more preferably from C1-C4-alkyl, C1-C4-alkoxy and NR15R16. In the group —C(═O)R12, R12 is specifically C1-C4-alkyl, such as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl or tert-butyl, preferably methyl, or is C1-C4-alkoxy, such as methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy or tert-butoxy, preferably methoxy, and is more specifically methyl, and in the group —S(O)2R12, R12 is specifically methyl. Preferably, R15 is hydrogen and R16 is selected from hydrogen, C1-C4-alkyl and phenyl, preferably from hydrogen and C1-C4-alkyl, or the two of R15 and R16 are C1-C4-alkyl.
R6 is preferably selected from hydrogen, C1-C4-alkyl, —C(═O)R12, —S(O)2R12, —CN, M and a group of the formula III, where R12 has one of the above general meanings or, in particular, one of the above preferred meanings and M has one of the above general meanings or, in particular, one of the below-given preferred meanings.
R6 is more preferably selected from hydrogen, C1-C4-alkyl, C3-C4-alkylcarbonyl, C1-C4-alkoxycarbonyl, —C(═O)N(H)C1-C4-alkyl, —C(═O)N(C1-C4-alkyl)2, C1-C4-alkylsulfonyl, CN and a group of the formula III. In particular, R6 is selected from hydrogen, CN, methylcarbonyl, methoxycarbonyl and methyl. Specifically, R6 is hydrogen.
M is preferably selected from an alkali metal cation, an earth alkaline metal cation equivalent, a cation equivalent of Cu, Zn, Fe or Ni or an ammonium cation of formula (NRaRbRcRd)+), wherein one of Ra, Rb, Rc and Rd is hydrogen and three of Ra, Rb, Rc and Rd, independently of each other, are selected from C1-C10-alkyl. More preferably, M is selected from Li+, Na+, K+, ½Mg2+, a cation equivalent of Cu, Zn, Fe or Ni and an ammonium cation of formula (NRaRbRcRd)+, wherein one of Ra, Rb, Rc and Rd is hydrogen and three of Ra, Rb, Rc and Rd, independently of each other, are selected from C1-C10-alkyl. Even more preferably, M is selected from Na+, K+, ½Mg2+; ½Cu2+; ½Zn2+; ½Fe2+; ½Ni2+, triethylammonium and trimethylammonium.
In the group of formula III, the variables preferably have the same meanings as in the remainder of the molecule I. Thus, the remarks made above as to preferred meanings of the radicals apply to this moiety, too.
R6a is preferably selected from hydrogen, C1-C10-alkyl, C1-C4-haloalkyl, phenyl, phenyl-C1-C4-alkyl, —C(═O)R12 and —S(O)2R12, where R12 has one of the above given general or, in particular, one of the above-given preferred meanings. More preferably, R6a is selected from hydrogen, C1-C4-alkyl, C1-C4-haloalkyl, phenyl, benzyl, —C(═O)R12 and —S(O)2R12, where R12 has one of the above given general or, in particular, one of the above-given preferred meanings, and more preferably from hydrogen, C1-C4-alkyl, C1-C4-haloalkyl, —C(═O)R12 and —S(O)2R12, where R12 has one of the above given general or, in particular, one of the above-given preferred meanings. In particular, R6a is hydrogen, C1-C4-alkyl, preferably methyl, or —C(═O)R12, more particularly hydrogen, C1-C4-alkyl, preferably methyl, methylcarbonyl or methoxycarbonyl, even more particularly hydrogen or C1-C4-alkyl, preferably methyl, and is specifically hydrogen.
If m is 1, the oxygen atom is preferably bound via a double bond to the sulfur atom, the radical —S(O)m—R6 thus resulting in a group —S(═O)—R6. If m is 2, the two oxygen atoms are preferably both bound via a double bond to the sulfur atom, the radical —S(O)m—R6 thus resulting in a group —S(═O)2—R6. If m is 3, the radical —S(O)m—R6 is a group —S(═O)2—O—R6.
m is preferably 0.
In a particularly preferred embodiment, in compounds I, m is 0 and R6 is H (or, alternatively, in compounds II, R6a is H).
Particularly preferred compounds I are compounds of formula I.A and I.B
wherein n is 3, 4 or 5 and R91, R92, R93, R94 and R95 are hydrogen or have one of the general or, in particular, one of the preferred meanings given for R9.
Preferably, in compounds I.A the combination of n, R91, R92, R93, R94 and R95 is as given in following table:
Preferably, in compounds I.B the combination of R91, R92, R93, R94 and R95 is as given in following table:
Particular compounds I/II/IA/IB are the following:
Examples for preferred compounds I and Hare compounds of formulae I.1 to I.10 and II.1 to II.5, where the variables have one of the general or, in particular, one of the preferred meanings given above. Examples of preferred compounds are the individual compounds compiled in the tables 1 to 2610 below. Moreover, the meanings mentioned below for the individual variables in the tables are per se, independently of the combination in which they are mentioned, a particularly preferred embodiment of the substituents in question.
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is H
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is methyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ethyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is propyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is isopropyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is n-butyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is sec-butyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is isobutyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is tert-butyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is phenyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is 4-methylphenyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is Li+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is Na+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is K+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ½Mg2+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ½Cu2+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ½Zn2+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ½Fe2+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ½Ni2+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is NH(CH3)3+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is NH(C2H5)3+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is NH(CH2CH2CH2)3+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is NH(CH(CH3)2)3+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is NH(CH2CH2CH2CH2)3+
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is methylcarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ethylcarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is propylcarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is isopropylcarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is methoxycarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ethoxycarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is propoxycarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is isopropoxycarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is phenoxycarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is methylaminocarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ethylaminocarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is propylaminocarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is isopropylaminocarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is phenylaminocarbonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is methylsulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ethylsulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is propylsulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is isopropylsulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is phenylsulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is methoxysulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is ethoxysulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is propoxysulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is isopropoxysulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is phenoxysulfonyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6 is CN
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6 is as defined in any of tables 1 to 49 and R1 is cyclopropyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6 is as defined in any of tables 1 to 49 and R1 is 1-methylcyclopropyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6 is as defined in any of tables 1 to 49 and R1 is 1-chlorocyclopropyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6 is as defined in any of tables 1 to 49 and R1 is cyclopropylmethyl
Compounds of the formula I.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6 is as defined in any of tables 1 to 49 and R1 is 1-cyclopropylethyl
Compounds of the formula I.2 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and the combination of R1 and R6 is as defined in any of tables 1 to 294
Compounds of the formula I.3 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and the combination of R1 and R6 is as defined in any of tables 1 to 294
Compounds of the formula I.4 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and the combination of R1 and R6 is as defined in any of tables 1 to 294
Compounds of the formula I.5 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and the combination of R1 and R6 is as defined in any of tables 1 to 294
Compounds of the formula I.6 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is tert-butyl
Compounds of the formula I.6 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is cyclopropyl
Compounds of the formula I.6 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is 1-methylcyclopropyl
Compounds of the formula I.6 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is 1-chlorocyclopropyl
Compounds of the formula I.6 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is cyclopropylmethyl
Compounds of the formula I.6 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is 1-cyclopropylethyl
Compounds of the formula I.7 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is as defined in any of tables 1471 to 1476
Compounds of the formula I.8 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is as defined in any of tables 1471 to 1476
Compounds of the formula I.9 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is as defined in any of tables 1471 to 1476
Compounds of the formula I.10 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and R1 is as defined in any of tables 1471 to 1476
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is H
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is methyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is ethyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is n-propyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is isopropyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is n-butyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is sec-butyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is isobutyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is tert-butyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is phenyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is 4-methylphenyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is methylcarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is ethylcarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is propylcarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is isopropylcarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is phenylcarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is methoxycarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is ethoxycarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is propoxycarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is isopropoxycarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is phenoxycarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is methylaminocarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is ethylaminocarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is propylaminocarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is isopropylaminocarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is phenylaminocarbonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is methylsulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is ethylsulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is propylsulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is isopropylsulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is phenylsulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is methoxysulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is ethoxysulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is propoxysulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is isopropoxysulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is phenoxysulfonyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R1 is tert-butyl and R6a is CN
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6a is as defined in any of tables 1501 to 1537 and R1 is cyclopropyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6a is as defined in any of tables 1501 to 1537 and R1 is 1-methylcyclopropyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6a is as defined in any of tables 1501 to 1537 and R1 is 1-chlorocyclopropyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6a is as defined in any of tables 1501 to 1537 and R1 is cyclopropylmethyl
Compounds of the formula II.1 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A, R6a is as defined in any of tables 1501 to 1537 and R1 is 1-cyclopropylethyl
Compounds of the formula II.2 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and the combination of R1 and R6a is as defined in any of tables 1501 to 1722
Compounds of the formula II.3 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and the combination of R1 and R6a is as defined in any of tables 1501 to 1722
Compounds of the formula II.4 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and the combination of R1 and R6a is as defined in any of tables 1501 to 1722
Compounds of the formula II.5 in which the combination of R91, R92, R93, R94 and R95 for a compound corresponds in each case to one row of Table A and the combination of R1 and R6a is as defined in any of tables 1501 to 1722
Among the above compounds, preference is given to compounds of formulae I.1, I.2, I.3, I.4, I.5, II.1 and II.2. More preference is given to compounds of formulae I.1, I.2, I.3, I.4, I.5, II.1 and II.2, wherein R1 is tert-butyl, and even more preference to compounds of formulae I.1, I.2, I.3, I.4, I.5, II.1 and II.2, wherein R1 is tert-butyl and R6 or R6a are hydrogen. Especial preference is given to compounds of formulae I.1, I.2, I.4, I.5, II.1, II.2, II.4 and II.5, in particular to compounds of formulae I.1, I.2, I.4, I.5, II.1, II.2, II.4 and II.5, wherein R1 is tert-butyl, and even more preference is given to compounds of formulae I.1, I.2, I.4, I.5, II.1, II.2, II.4 and II.5, wherein R1 is tert-butyl and R6 or R6a are hydrogen.
Compounds of formulae I and II can be prepared by one or more of the following methods and variations as described in schemes 1 to 6 and in the syntheses descriptions below. The variables are as defined above for formulae I and II.
Compounds of formula I, wherein R6 is H and m is 0 (or compounds II, wherein R68 is H), can be prepared by sulfurizing the corresponding triazole derivative IV as outlined in scheme 1. Sulfurization can be carried out in analogy to known processes, for example as described in WO 96/16048. For instance, the triazolyl ring can be first deprotonated with a strong base, e.g. an organolithium base, such as n-butyllithium, tert-butyllithium or sec-butyllithium, lithium diisopropyl amide, sodium hydride, sodium amide or potassium tert-butylate mixed with tetramethylethylene diamine (TMEDA), and then the resulting anion is reacted with elemental sulfur. Sulfur is generally used in powdered form. The reaction is generally carried out in an inert solvent, such as ethers, e.g. diethylether, methyl-tert-butylether, tetrahydrofuran or dioxane, dimethoxyethane, liquid ammonia, dimethylsulfoxide or dimethylformamide. The reaction temperature is not very critical and can range, for example, from −70 to +50° C., preferably from −70 to 0° C. Alternatively, sulfurization can be carried out in the absence of a base by reacting 7 with elemental sulfur in a high-boiling solvent, such as N-methylpyrrolidinone, dioxane or N,N-dimethylformamide, while heating, e.g. to 160 to 250° C. After completion of the reaction, the resulting mixture is hydrolyzed, e.g. by the addition of water or an aqueous acid, such as a mineral acid (e.g. dilute sulfuric acid or hydrochloric acid), acetic acid or ammoniumchloride, to give compound I.
The triazole compound IV, wherein R2 is H, can be prepared in analogy to known methods, such as described, for example, in DE-A-3702301, as outlined in scheme 2. For instance, the oxirane compound I and [1,2,4]-1H-triazole can be reacted in the presence of a base, such as an alkali metal hydride (e.g. sodium hydride, potassium hydride), an alkali metal hydroxide (e.g. sodium hydroxide, potassium hydroxide), or an alkali metal carbonate (e.g. sodium carbonate, potassium carbonate, caesium carbonate). The reaction is suitably carried out in a solvent. Suitable solvents are, for example, toluene, N-methypyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran), alcohols (e.g. methanol, ethanol, isopropanol or tert-butanol), acetonitrile, or N,N-dimethylformamide.
The oxirane 1 in turn can be prepared in analogy to known methods, such as described, for example, in EP-A-0267778, Org. Syn. 49, 78 (1968) or J. Am. Chem. Soc. 1975, 1353, as outlined in scheme 3 below. For instance, the ketone 2 may be reacted with a sulfonium ylide or an oxosulfonium ylide, such as dimethyloxosulfonium methylide or dimethylsulfonium methylide in a solvent. Alternatively, the oxirane 1 can be prepared in an epoxidation reaction in analogy to the method described in Tetrahedron Lett. 23, 5283 (1982) or in EP-A-0655443 by subjecting 2 to the reaction with a trimethylsulfonium salt, such as trimethylsulfonium bromide, trimethylsulfonium iodide or methyltrimethylsulfonium sulfate, in the presence of a metal oxide, such as alkaline metal oxides (e.g. sodium oxide, potassium oxide), alkaline earth metal oxides (e.g. magnesium oxide, calcium oxide, barium oxide) or zinc oxide, and optionally a base, such as alkali metal hydrides (e.g. sodium hydride, potassium hydride), alkali metal hydroxides (e.g. sodium hydroxide, potassium hydroxide), alkali metal carbonates (e.g. sodium carbonate, potassium carbonate, caesium carbonate) in a two-phase solid/liquid system comprising an organic solvent, such as toluene, N-methypyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran), acetonitrile or N,N-dimethylformamide. Alternatively, the oxirane 1 can be prepared in analogy to the method described in Tetrahedron 1985, 1259 by epoxidation of 2 with a trimethylsulfonium salt, such as trimethylsulfonium bromide, trimethylsulfonium iodide or methyltrimethylsulfonium sulfate, or a trimethylsulfoxonium salt, such as trimethylsulfoxonium bromide, trimethylsulfoxonium iodide or methyltrimethylsulfoxonium sulfate and potassium sulfate/aluminium oxide.
The ketone 2 can be obtained from the halide 4 by a Grignard reaction with the aldehyde 5, as outlined in scheme 4 below. Oxidation of the obtained alcohol 3 via known methods, such as oxidation with the Swern reagent, hypervalent iodine compounds (IBX, Martin's reagent), chromine compounds (e.g. pyridinium dichromate, pyridinium chlorochromate, dipyridinium chromine trioxide), sodium hypochlorite and the like, yields the ketone 2.
As an alternative to the process described in scheme 3, the oxirane 1 can be prepared in analogy to the method described in Org. Syn. 40, 66, 1966, J. Org. Chem. 28, 1128, 1963 and Org. Syn. Coll. Vol. 4, 552, 1963 as outlined in scheme 5 below by first subjecting the ketone 2 to a Wittig reaction, thus yielding the corresponding olefinic compound 6, and then subjecting this to an epoxidation reaction. The Wittig reaction can be carried out under standard conditions, such as the use of methyltriphenylphosphonium bromide or iodide in the presence of an alkali metal base, such as n-butyllithium, secbutyllithium or tert-butyllithium. Epoxidation can also be carried out with standard reagents, such as peracetic acid, perbenzoic acid meta-chloroperbenzoic acid, perphthalic acid and the like. Olefination (i.e. transformation of the C═0 into a C═CH2 group) of 5 can alternatively be achieved by the use of Tebbe's reagent ((C5H5)2TiCH2ClAl(CH3)2).
As an alternative to the process described in scheme 1, compounds I, wherein R6 is H and m is 0 (or compounds II, wherein R6a is H), can also be prepared in analogy to the method described in WO 99/18088 as outlined in scheme 6 below. Epoxide opening of 1 with hydrazine, optionally in the presence of an acid (e.g. hydrochloric acid, hydrobromic acid, acetic acid, sulfuric acid or p-toluenesulfonic acid) or a base (e.g. triethylamine, diisopropylethylamine, sodium carbonate or potassium carbonate) in a suitable solvent, such as an alcohol (e.g. methanol, ethanol, isopropanol, tert-butanol), N-methylpyrrolidinone, an ether (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide or dimethylsulfoxide, yields 7. This is then converted into the semicarbazide 8 by reaction with a thiocyanate, such as sodium thiocyanate, potassium thiocyanate or ammonium thiocyanate (i.e. M+=e.g. Na+, K+, NH4+), in a suitable solvent, such as an alcohol (e.g. methanol, ethanol, isopropanol, tert-butanol), N-methylpyrrolidinone, an ether (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide, dimethylsulfoxide, toluene or xylene. The semicarbazide is then converted into I/II via reaction with a formic acid alkyl ester (e.g. formic acid methyl ester, formic acid ethyl ester) in a solvent. Suitable solvents are, for example, alcohols (e.g. methanol, ethanol, isopropanol, tert-butanol), N-methylpyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide, dimethylsulfoxide, toluene or xylene. Alternatively, 7 can be reacted with hydrogen thiocyanate and formaldehyde in a solvent. Suitable solvents are, for example, alcohols (e.g. methanol, ethanol, isopropanol, tert-butanol), N-methylpyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide, dimethylsulfoxide, toluene or xylene. The resulting triazolidinthione 9 is then oxidized using, for example, FeCl3 in an aqueous acid (e.g. hydrochloric acid) or oxygen in the presence of an alkali metal hydroxide (e.g. sodium hydroxide, potassium hydroxide) and elemental sulfur to I/II. In a yet further alternative, 7 is reacted with a dialkyl ketone (e.g. acetone, diethylketone, methyl ethyl ketone) and a thiocyanate (e.g. sodium thiocyanate, potassium thiocyanate, ammonium thiocyanate) in a solvent to give the triazolidinthione 10. Suitable solvents are, for example, alcohols (e.g. methanol, ethanol, isopropanol, tert-butanol), N-methylpyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide, dimethylsulfoxide, toluene or xylene. The triazolidinthione 10 is then converted into I/II by reaction with formic acid in the presence of an acid (e.g. hydrochloric acid, hydrobromic acid, acetic acid, sulfuric acid, p-toluenesulfonic acid) or a metal oxide (e.g. amorphous TiO2).
The halide 4 and the aldehyde 5 used in the above reactions are either commercially available or can be produced by standard methods known to the skilled person.
Compounds of formula I, wherein R6 is different from hydrogen and m is 0, can be prepared from compounds I (wherein R6═H and m=0).
Compounds of formula I, wherein m is 0 and R6 is C1-C10-alkyl, C2-C10-alkenyl, C2-C10-haloalkenyl, C2-C10-alkynyl, C2-C10-haloalkynyl, C3-C10-cycloalkyl, C3-C10-halocycloalkyl, phenyl, phenyl-C1-C4-alkyl, where the phenyl moiety in the 2 last-mentioned radicals may be substituted as described above, and a 5- or 6-membered saturated, partially unsaturated or aromatic heterocyclic ring containing 1, 2 or 3 heteroatoms selected from N, O and S as ring members, where the heterocyclic ring may be substituted as described above, may be prepared in analogy to the method described in DE-A-19520098 by reacting a compound I, wherein m is 0 and R6 is H, with a compound R6-LG, where R6 has one of the above meanings and LG is a leaving group, such as a halide (e.g. Cl, Br, I), a tosylate or a mesylate, in the presence of a base. Suitable bases are, for example, alkali metal hydrides (e.g. sodium hydride, potassium hydride), alkali metal hydroxides (e.g. sodium hydroxide, potassium hydroxyide), alkali metal carbonates (e.g. sodium carbonate, potassium carbonate, caesium carbonate), alkali metal alkoxides (e.g. sodium methoxide, potassium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide) or organolithium bases (e.g. n-butyl lithium, sec-butyl lithium, tert-butyl lithium and lithium diisopropylamine). The reaction is generally carried out in a suitable solvent. Suitable solvents are, for example, toluene, N-methylpyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide or dimethylsulfoxide.
Alternatively, compounds of formula I, wherein m is 0 and R6 is C1-C10-alkyl, C1-C10-haloalkyl, C2-C10-alkenyl, C2-C10-haloalkenyl, C2-C10-alkynyl, C2-C10-haloalkynyl, C3-C10-cycloalkyl, C3-C10-halocycloalkyl, phenyl, phenyl-C1-C4-alkyl, where the phenyl moiety in the 2 last-mentioned radicals may be substituted as described above, and a 5- or 6-membered saturated, partially unsaturated or aromatic heterocyclic ring containing 1, 2 or 3 heteroatoms selected from N, O and S as ring members, where the heterocyclic ring may be substituted as described above, may be prepared in analogy to the method described in Heterocycles, 23(7), 1645-1649, 1985 by reacting compound IV with a disulfide R6—S—S—R6 in the presence of a strong base under conditions similar to those described for scheme 1.
Compounds of formulae I, wherein m is 0 and R6 is —C(═O)R12 or —C(═S)R12, may be prepared in analogy to the method described in DE-A-19617461 by reacting a compound I, wherein m is 0 and R6 is H, with a compound R12—C(═O)—W, R12—C(═S)—W, R12′—N═C═O or R12′—N═C═S, wherein R12 has one of the above meanings, R12′ is C1-C10-alkyl or C1-C10-haloalkyl and W is a good leaving group, such as a halide (e.g. Cl, Br, I), an alkoxide (e.g. methoxide, ethoxide) or pentafluorophenoxide, in the presence of a base. Suitable bases are, for example, alkali metal hydrides (e.g. sodium hydride, potassium hydride), alkali metal hydroxides (e.g. sodium hydroxide, potassium hydroxyide), alkali metal carbonates (e.g. sodium carbonate, potassium carbonate, caesium carbonate), alkali metal alkoxides (e.g. sodium methoxide, potassium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide) or organolithium bases (e.g. n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamine). The reaction is generally carried out in a suitable solvent. Suitable solvents are, for example, toluene, N-methylpyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide or dimethylsulfoxide.
Compounds of formula I, wherein m is 0 and R6 is —SO2R12, may be prepared in analogy to the method described in DE-A-19620590 by reacting a compound I, wherein m is 0 and R6 is H, with a compound R12—SO2—W, wherein R12 has one of the above meanings and W is a good leaving group, such as a halide (e.g. Cl, Br, I), an alkoxide (e.g. methoxide, ethoxide) or pentafluorophenoxide, in the presence of a base. Suitable bases are, for example, alkali metal hydrides (e.g. sodium hydride, potassium hydride), alkali metal hydroxides (e.g. sodium hydroxide, potassium hydroxide), alkali metal carbonates (e.g. sodium carbonate, potassium carbonate, caesium carbonate), alkali metal alkoxides (e.g. sodium methoxide, potassium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide) or organolithium bases (e.g. n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamine). The reaction is generally carried out in a suitable solvent. Suitable solvents are, for example, toluene, N-methylpyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide or dimethylsulfoxide.
Compounds of formula I, wherein m is 0 and R6 is —CN, may be prepared in analogy to the method described in DE-A-19620407 by reacting a compound I, wherein m is 0 and R6 is H, with a compound CN—W, wherein W is a good leaving group, such as a halide (e.g. Cl, Br, I), in the presence of a base. Suitable bases are, for example, alkali metal hydrides (e.g. sodium hydride, potassium hydride), alkali metal hydroxides (e.g. sodium hydroxide, potassium hydroxide), alkali metal carbonates (e.g. sodium carbonate, potassium carbonate, caesium carbonate), alkali metal alkoxides (e.g. sodium methoxide, potassium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide) or organolithium bases (e.g. n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamine). The reaction is generally carried out in a suitable solvent. Suitable solvents are, for example, toluene, N-methylpyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide or dimethylsulfoxide.
Compounds of formula I, wherein m is 0 and R6 is M, may be prepared in analogy to the method described in DE-A-19617282 by reacting a compound I with an amine NRaRbRc, wherein Ra, Rb and Rc are as defined above, or with a metal salt, such as sodium hydroxide, potassium hydroxide or copper acetate.
Compounds of formula I, wherein m is 0 and R6 is a group of formula III, may be prepared in analogy to the method described in WO 97/43269 by reacting a compound I, wherein m is 0 and R6 is H, with a halogen, especially iodine, in the presence of a base. Suitable bases are, for example, alkali metal hydrides (e.g. sodium hydride, potassium hydride), alkali metal hydroxides (e.g. sodium hydroxide, potassium hydroxyide), alkali metal carbonates (e.g. sodium carbonate, potassium carbonate, caesium carbonate), alkali metal alkoxides (e.g. sodium methoxide, potassium methoxide, sodium ethoxide, potassium ethoxide, potassium tert-butoxide) or organolithium bases (e.g. n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamine). The reaction is generally carried out in a suitable solvent. Suitable solvents are, for example, toluene, N-methylpyrrolidinone, ethers (e.g. diethyl ether, tetrahydrofuran, dioxane, 1,2-dimethoxyethane), acetonitrile, N,N-dimethylformamide or dimethylsulfoxide.
Compounds of formula I, wherein m is 0 and R6 is —P(═O)R13R14, may be prepared in analogy to the method described in WO 99/05149.
Compounds of formula II, wherein R6a is hydrogen (or compounds of formula I, wherein m is 0 and R6 is hydrogen), can be prepared in analogy to the method described in WO 99/18087 by reacting a triazolidinthione 9 with an oxidizing agent, optionally in the presence of a catalyst. Suitable oxidizing agents are, for example, oxygen, sulfur and potassium superoxide. Especially in case oxygen is used as oxidizing agent, it is advantageous to carry out the oxidation reaction in the presence of a catalyst. A suitable catalyst is, for example, a mixture of powdery sulfur and KOH. The reaction is generally carried out in a suitable solvent. Suitable solvents are, for example, aliphatic hydrocarbons (e.g. pentane, hexane), cycloaliphatic hydrocarbons (e.g. cyclohexane), aromatic hydrocarbons (e.g. bemzene, toluene, the xylenes), ethers (e.g. diethylether, methyl-tert-butylether), and esters (e.g. ethylecetate, propylacetate, n-butylacetate).
The oxidation of the triazolidinthione 9 may also be carried out with ferric chloride (FeCl3) in an acidic aqueous solution in analogy to the method described in WO 01/46158. The reaction is generally carried out in a suitable solvent. Suitable solvents are, for example, ethanol, ethylacetate and mixtures of ethanol with toluene.
The oxidation of the triazolidinthione 9 may also be carried out with formic acid, optionally in the presence of a catalyst, in analogy to the method described in WO 99/18086 or WO 99/18088. Suitable catalysts are, for example, acids, like hydrochloric acid, sulfuric acid or p-toluenesulfonic acid, and metal oxides, like amorphous titanium dioxide. The reaction is generally carried out in a suitable solvent. Suitable solvents are weakly polar solvents like, for example, alcohols such as propanol, butanol and pentanol, esters, like ethyl acetate, butyl acetate and isobutyl formate, ethers, like 1,2-dimethoxyethane, methyl-tert-butyl ether and methyl-tert-amylether, and formic acid used in excess.
Compounds of formula II, wherein R6a is different from hydrogen, can be prepared by reacting the NR6a group, wherein R6a is H, in analogy to the above-described conversion of compounds I, wherein R6 is H, into compounds, wherein R6 is different from H.
Compounds I, wherein m is 1 or 2, can be prepared from respective compounds I, wherein m is 0, by oxidation. Alternatively, compounds I, wherein m is 2, can be prepared from compounds IV by first deprotonating the triazolyl ring and then reacting with a sulfonyl chloride R6SO2Cl. Compounds I, wherein m is 3, can be prepared from compounds IV by first deprotonating the triazolyl ring and then reacting with sulfuric acid chloride or a sulfuric ester chloride of formula R6OSO2Cl, wherein R6 is selected from hydrogen, C1-C10-alkyl, C1-C10-haloalkyl, C2-C10-alkenyl, C2-C10-haloalkenyl, C2-C10-alkynyl, C2-C10-haloalkynyl, C3-C10-cycloalkyl, C3-C10-halocycloalkyl, phenyl, phenyl-C1-C4-alkyl, where the phenyl moiety in the 2 last-mentioned radicals may be substituted as mentioned above, and a 5- or 6-membered saturated, partially unsaturated or aromatic heterocyclic ring containing 1, 2 or 3 heteroatoms selected from N, O and S, wherein the heterocyclic ring may be substituted as mentioned above.
Compounds of formula I or II, wherein R2 is different from hydrogen, can be prepared by introducing a protective group R2 by known means in any reaction step in which the protection of the OH group is required or advantageous. Deprotection to R2═H can be carried out by any known means.
If individual compounds cannot be prepared via the above-described routes, they can be prepared by derivatization of other compounds I and II or by customary modifications of the synthesis routes described.
The reaction mixtures are worked up in the customary manner, for example by mixing with water, separating the phases, and, if appropriate, purifying the crude products by chromatography, for example on alumina or silica gel. Some of the intermediates and end products may be obtained in the form of colorless or pale brown viscous oils, which are freed or purified from volatile components under reduced pressure and at moderately elevated temperature. If the intermediates and end products are obtained as solids, they may be purified by recrystallization or digestion.
A further aspect of the invention relates to compounds of formula IV
wherein R1, R2, R3, R4, R5 and n have one of the general or, in particular, one of the preferred meanings given above for compounds I and II; except for the compound wherein R1 is n-propyl, R2 is H, R3 and R4 are H, R5 is phenyl and n is 3.
In compounds IV, R1 is preferably selected from tert-butyl, phenyl, cyclopropyl, 1-methylcyclopropyl, 1-chlorocyclopropyl and 1-cyclopropylethyl and is more preferably tert-butyl.
Compounds IV are on the one side valuable intermediates in the preparation of compounds I and II (see above schemes), but on the other side show a remarkable fungicidal activity, too.
Particularly preferred compounds IV are compounds of formulae IV.1 to IV.5, wherein the combination of R91, R92, R93, R94 and R95 corresponds in each case to one row in table A above and R1 is tert-butyl, cyclopropyl, 1-methylcyclopropyl, 1-chlorocyclopropyl, cyclopropylmethyl or 1-cyclopropylethyl.
A further aspect of the invention relates to compounds of formula 7
wherein R1, R3, R4, R5 and n have one of the general or, in particular, one of the preferred meanings given above for compounds I and II.
Compounds 7 are valuable intermediates in the preparation of compounds I and II (see above schemes).
A further aspect of the invention relates to compounds of formula 1
wherein R1, R3, R4, R5 and n have one of the general or, in particular, one of the preferred meanings given above for compounds I and II.
Compounds 1 are valuable intermediates in the preparation of compounds I and II (see above schemes).
The invention further refers to an agricultural composition comprising at least one compound of formula I, II and/or IV as defined above or an agriculturally acceptable salt thereof and a liquid or solid carrier. Suitable carriers, as well as auxiliaries and further active compounds which may also be contained in the composition of the invention are defined below.
The compounds I and II as well as IV and the compositions according to the invention, respectively, are suitable as fungicides. They are distinguished by an outstanding effectiveness against a broad spectrum of phytopathogenic fungi, including soil-borne fungi, which derive especially from the classes of the Plasmodiophoromycetes, Peronosporomycetes (syn. Oomycetes), Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes (syn. Fungi imperfecti). Some are systemically effective and they can be used in crop protection as foliar fungicides, fungicides for seed dressing and soil fungicides. Moreover, they are suitable for controlling harmful fungi, which inter alia occur in wood or roots of plants.
The compounds I, II and IV and the compositions according to the invention are particularly important in the control of a multitude of phytopathogenic fungi on various cultivated plants, such as cereals, e.g. wheat, rye, barley, triticale, oats or rice; beet, e.g. sugar beet or fodder beet; fruits, such as pomes, stone fruits or soft fruits, e.g. apples, pears, plums, peaches, almonds, cherries, strawberries, raspberries, blackberries or gooseberries; leguminous plants, such as lentils, peas, alfalfa or soybeans; oil plants, such as rape, mustard, olives, sunflowers, coconut, cocoa beans, castor oil plants, oil palms, ground nuts or soybeans; cucurbits, such as squashes, cucumber or melons; fiber plants, such as cotton, flax, hemp or jute; citrus fruit, such as oranges, lemons, grapefruits or mandarins; vegetables, such as spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, cucurbits or paprika; lauraceous plants, such as avocados, cinnamon or camphor; energy and raw material plants, such as corn, soybean, rape, sugar cane or oil palm; corn; tobacco; nuts; coffee; tea; bananas; vines (table grapes and grape juice grape vines); hop; turf; natural rubber plants or ornamental and forestry plants, such as flowers, shrubs, broad-leaved trees or evergreens, e.g. conifers; and on the plant propagation material, such as seeds, and the crop material of these plants.
Preferably, compounds I, II and IV and compositions thereof, respectively are used for controlling a multitude of fungi on field crops, such as potatoes sugar beets, tobacco, wheat, rye, barley, oats, rice, corn, cotton, soybeans, rape, legumes, sunflowers, coffee or sugar cane; fruits; vines; ornamentals; or vegetables, such as cucumbers, tomatoes, beans or squashes.
The term “plant propagation material” is to be understood to denote all the generative parts of the plant such as seeds and vegetative plant material such as cuttings and tubers (e.g. potatoes), which can be used for the multiplication of the plant. This includes seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants, including seedlings and young plants, which are to be transplanted after germination or after emergence from soil. These young plants may also be protected before transplantation by a total or partial treatment by immersion or pouring.
Preferably, treatment of plant propagation materials with compounds I, II and IV and compositions thereof, respectively, is used for controlling a multitude of fungi on cereals, such as wheat, rye, barley and oats; rice, corn, cotton and soybeans.
The term “cultivated plants” is to be understood as including plants which have been modified by breeding, mutagenesis or genetic engineering including but not limiting to agricultural biotech products on the market or in development (cf. http://www.bio.org/speeches/pubs/er/agri_products.asp). Genetically modified plants are plants, which genetic material has been so modified by the use of recombinant DNA techniques that under natural circumstances cannot readily be obtained by cross breeding, mutations or natural recombination. Typically, one or more genes have been integrated into the genetic material of a genetically modified plant in order to improve certain properties of the plant. Such genetic modifications also include but are not limited to targeted post-translational modification of protein(s), oligo- or polypeptides e.g. by glycosylation or polymer additions such as prenylated, acetylated or farnesylated moieties or PEG moieties.
Plants that have been modified by breeding, mutagenesis or genetic engineering, e.g. have been rendered tolerant to applications of specific classes of herbicides, such as hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors; acetolactate synthase (ALS) inhibitors, such as sulfonyl ureas (see e.g. U.S. Pat. No. 6,222,100, WO 01/82685, WO 00/26390, WO 97/41218, WO 98/02526, WO 98/02527, WO 04/106529, WO 05/20673, WO 03/14357, WO 03/13225, WO 03/14356, WO 04/16073) or imidazolinones (see e.g. U.S. Pat. No. 6,222,100, WO 01/82685, WO 00/026390, WO 97/41218, WO 98/002526, WO 98/02527, WO 04/106529, WO 05/20673, WO 03/014357, WO 03/13225, WO 03/14356, WO 04/16073); enolpyruvylshikimate-3-phosphate synthase (EPSPS) inhibitors, such as glyphosate (see e.g. WO 92/00377); glutamine synthetase (GS) inhibitors, such as glufosinate (see e.g. EP-A 242 236, EP-A 242 246) or oxynil herbicides (see e.g. U.S. Pat. No. 5,559,024) as a result of conventional methods of breeding or genetic engineering. Several cultivated plants have been rendered tolerant to herbicides by conventional methods of breeding (mutagenesis), e.g. Clearfield® summer rape (Canola, BASF SE, Germany) being tolerant to imidazolinones, e.g. imazamox. Genetic engineering methods have been used to render cultivated plants, such as soybean, cotton, corn, beets and rape, tolerant to herbicides such as glyphosate and glufosinate, some of which are commercially available under the trade names RoundupReady® (glyphosate-tolerant, Monsanto, U.S.A.) and LibertyLink® (glufosinatetolerant, Bayer CropScience, Germany).
Furthermore, plants are also covered that, by the use of recombinant DNA techniques, are capable to synthesize one or more insecticidal proteins, especially those known from the bacterial genus Bacillus, particularly from Bacillus thuringiensis, such as δ-endotoxins, e.g. CryIA(b), CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c; vegetative insecticidal proteins (VIP), e.g. VIP1, VIP2, VIP3 or VIP3A; insecticidal proteins of bacteria colonizing nematodes, e.g. Photorhabdus spp. or Xenorhabdus spp.; toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins; toxins produced by fungi, such Streptomycetes toxins, plant lectins, such as pea or barley lectins; agglutinins; proteinase inhibitors, such as trypsin inhibitors, serine protease inhibitors, patatin, cystatin or papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroid oxidase, ecdysteroid-IDP-glycosyl-transferase, cholesterol oxidases, ecdysone inhibitors or HMG-CoA-reductase; ion channel blockers, such as blockers of sodium or calcium channels; juvenile hormone esterase; diuretic hormone receptors (helicokinin receptors); stilben synthase, bibenzyl synthase, chitinases or glucanases. In the context of the present invention these insecticidal proteins or toxins are to be understood expressly also as pre-toxins, hybrid proteins, truncated or otherwise modified proteins. Hybrid proteins are characterized by a new combination of protein domains, (see, e.g. WO 02/015701). Further examples of such toxins or genetically modified plants capable of synthesizing such toxins are disclosed, e.g., in EP-A 374 753, WO 93/007278, WO 95/34656, EP-A 427 529, EP-A 451 878, WO 03/18810 and WO 03/52073. The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e.g., in the publications mentioned above. These insecticidal proteins contained in the genetically modified plants impart to the plants producing these proteins tolerance to harmful pests from all taxonomic groups of arthropods, especially to beetles (Coleoptera), two-winged insects (Diptera), and moths (Lepidoptera) and to nematodes (Nematoda). Genetically modified plants capable to synthesize one or more insecticidal proteins are, e.g., described in the publications mentioned above, and some of them are commercially available such as YieldGard® (corn cultivars producing the Cry1Ab toxin), YieldGard® Plus (corn cultivars producing Cry1Ab and Cry3Bb1 toxins), Starlink® (corn cultivars producing the Cry9c toxin), Herculex® RW (corn cultivars producing Cry34Ab1, Cry35Ab1 and the enzyme Phosphinothricin-N-Acetyltransferase [PAT]); NuCOTN® 33B (cotton cultivars producing the Cry1Ac toxin), Bollgard® I (cotton cultivars producing the Cry1Ac toxin), Bollgard® II (cotton cultivars producing Cry1Ac and Cry2Ab2 toxins); VIPCOT® (cotton cultivars producing a VIP-toxin); NewLeaf® (potato cultivars producing the Cry3A toxin); BtXtra®, NatureGard®, KnockOut®, BiteGard®, Protecta®, Bt11 (e.g. Agrisure® CB) and Bt176 from Syngenta Seeds SAS, France, (corn cultivars producing the Cry1Ab toxin and PAT enzyme), MIR604 from Syngenta Seeds SAS, France (corn cultivars producing a modified version of the Cry3A toxin, c.f. WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium (corn cultivars producing the Cry3Bb1 toxin), IPC 531 from Monsanto Europe S.A., Belgium (cotton cultivars producing a modified version of the Cry1Ac toxin) and 1507 from Pioneer Overseas Corporation, Belgium (corn cultivars producing the Cry1F toxin and PAT enzyme).
Furthermore, plants are also covered that, by the use of recombinant DNA techniques, are capable to synthesize one or more proteins to increase the resistance or tolerance of those plants to bacterial, viral or fungal pathogens. Examples of such proteins are the so-called “pathogenesis-related proteins” (PR proteins, see, e.g. EP-A 392 225), plant disease resistance genes (e.g. potato cultivars, which express resistance genes acting against Phytophthora infestans derived from the Mexican wild potato Solanum bulbocastanum) or T4-lysozym (e.g. potato cultivars capable of synthesizing these proteins with increased resistance against bacteria such as Erwinia amylvora). The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e.g., in the publications mentioned above.
Furthermore, plants are also covered that, by the use of recombinant DNA techniques, are capable to synthesize one or more proteins to increase the productivity (e.g. bio mass production, grain yield, starch content, oil content or protein content), tolerance to drought, salinity or other growth-limiting environmental factors or tolerance to pests and fungal, bacterial or viral pathogens of those plants.
Furthermore, plants are also covered that, by the use of recombinant DNA techniques, contain a modified amount of substances of content or new substances of content, specifically to improve human or animal nutrition, e.g. oil crops that produce health-promoting long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids (e.g. Nexera® rape, DOW Agro Sciences, Canada).
Furthermore, plants are also covered that, by the use of recombinant DNA techniques, contain a modified amount of substances of content or new substances of content, specifically to improve raw material production, e.g. potatoes that produce increased amounts of amylopectin (e.g. Amflora® potato, BASF SE, Germany).
The compounds I, II and IV and compositions thereof, respectively, are particularly suitable for controlling the following plant diseases:
Albugo spp. (white rust) on ornamentals, vegetables (e.g. A. candida) and sunflowers (e.g. A. tragopogonis); Altemana spp. (Alternaria leaf spot) on vegetables, rape (A. brassicola or brassicae), sugar beets (A. tenuis), fruits, rice, soybeans, potatoes (e.g. A. solani or A. alternata), tomatoes (e.g. A. solani or A. alternata) and wheat; Aphanomyces spp. on sugar beets and vegetables; Ascochyta spp. on cereals and vegetables, e.g. A. tritici (anthracnose) on wheat and A. hordei on barley; Bipolaris and Drechslera spp. (teleomorph: Cochliobolus spp.), e.g. Southern leaf blight (D. maydis) or Northern leaf blight (B. zeicola) on corn, e.g. spot blotch (B. sorokiniana) on cereals and e.g. B. oryzae on rice and turfs; Blumeria (formerly Erysiphe) graminis (powdery mildew) on cereals (e.g. on wheat or barley); Botrytis cinerea (teleomorph: Botryotinia fuckeliana: grey mold) on fruits and berries (e.g. strawberries), vegetables (e.g. lettuce, carrots, celery and cabbages), rape, flowers, vines, forestry plants and wheat; Bremia lactucae (downy mildew) on lettuce; Ceratocystis (syn. Ophiostoma) spp. (rot or wilt) on broad-leaved trees and evergreens, e.g. C. ulmi (Dutch elm disease) on elms; Cercospora spp. (Cercospora leaf spots) on corn (e.g. Gray leaf spot: C. zeae-maydis), rice, sugar beets (e.g. C. beticola), sugar cane, vegetables, coffee, soybeans (e.g. C. sojina or C. kikuchii) and rice; Cladosporium spp. on tomatoes (e.g. C. fulvum: leaf mold) and cereals, e.g. C. herbarum (black ear) on wheat; Claviceps purpurea(ergot) on cereals; Cochliobolus (anamorph: Helminthosporium of Bipolaris) spp. (leaf spots) on corn (C. carbonum), cereals (e.g. C. sativus, anamorph: B. sorokiniana) and rice (e.g. C. miyabeanus, anamorph: H. oryzae); Colletotrichum (teleomorph: Glomerella) spp. (anthracnose) on cotton (e.g. C. gossypii), corn (e.g. C. graminicola: Anthracnose stalk rot), soft fruits, potatoes (e.g. C. coccodes: black dot), beans (e.g. C. lindemuthianum) and soybeans (e.g. C. truncatum or C. gloeosporioides); Corticium spp., e.g. C. sasakii (sheath blight) on rice; Corynespora cassiicola (leaf spots) on soybeans and ornamentals; Cycloconium spp., e.g. C. oleaginum on olive trees; Cylindrocarpon spp. (e.g. fruit tree canker or young vine decline, teleomorph: Nectria or Neonectria spp.) on fruit trees, vines (e.g. C. liriodendri, teleomorph: Neonectria liriodendri: Black Foot Disease) and ornamentals; Dematophora (teleomorph: Rosellinia) necatrix (root and stem rot) on soybeans; Diaporthe spp., e.g. D. phaseolorum (damping off) on soybeans; Drechslera (syn. Helminthosporium, teleomorph: Pyrenophora) spp. on corn, cereals, such as barley (e.g. D. teres, net blotch) and wheat (e.g. D. tritici-repentis: tan spot), rice and turf; Esca (dieback, apoplexy) on vines, caused by Formitiporia (syn. Phellinus) punctata, F. mediterranea, Phaeomoniella chlamydospora (earlier Phaeoacremonium chlamydosporum), Phaeoacremonium aleophilum and/or Botryosphaeria obtusa; Elsinoe spp. on pome fruits (E. pyri), soft fruits (E. veneta: anthracnose) and vines (E. ampelina: anthracnose); Entyloma oryzae (leaf smut) on rice; Epicoccum spp. (black mold) on wheat; Erysiphe spp. (powdery mildew) on sugar beets (E. betae), vegetables (e.g. E. pisi), such as cucurbits (e.g. E. cichoracearum), cabbages, rape (e.g. E. cruciferarum); Eutypa lata (Eutypa canker or dieback, anamorph: Cytosporina lata, syn. Libertella blepharis) on fruit trees, vines and ornamental woods; Exserohilum (syn. Helminthosporium) spp. on corn (e.g. E. turcicum); Fusarium (teleomorph: Gibberella) spp. (wilt, root or stem rot) on various plants, such as F. graminearum or F. culmorum (root rot, scab or head blight) on cereals (e.g. wheat or barley), F. oxysporum on tomatoes, F. solani on soybeans and F. verticilliodes on corn; Gaeumannomyces graminis (take-all) on cereals (e.g. wheat or barley) and corn; Gibberella spp. on cereals (e.g. G. zeae) and rice (e.g. G. fujikuroi: Bakanae disease); Glomerella cingulata on vines, pome fruits and other plants and G. gossypii on cotton; Grain-staining complex on rice; Guignardia bidwellii (black rot) on vines; Gymnosporangium spp. on rosaceous plants and junipers, e.g. G. sabinae (rust) on pears; Helminthosporium spp. (syn. Drechslera, teleomorph: Cochliobolus) on corn, cereals and rice; Hemileia spp., e.g. H. vastatrix (coffee leaf rust) on coffee; Isariopsis clavispora (syn. Cladosporium vitis) on vines; Macrophomina phaseolina (syn. phaseoli) (root and stem rot) on soybeans and cotton; Microdochium (syn. Fusarium) nivale (pink snow mold) on cereals (e.g. wheat or barley); Microsphaera diffusa (powdery mildew) on soybeans; Monilinia spp., e.g. M. laxa, M. fructicola and M. fructigena (bloom and twig blight, brown rot) on stone fruits and other rosaceous plants; Mycosphaerella spp. on cereals, bananas, soft fruits and ground nuts, such as e.g. M. graminicola (anamorph: Septoria tritici, Septoria blotch) on wheat or M. fijiensis (black Sigatoka disease) on bananas; Peronospora spp. (downy mildew) on cabbage (e.g. P. brassicae), rape (e.g. P. parasitica), onions (e.g. P. destructor), tobacco (P. tabacina) and soybeans (e.g. P. manshurica); Phakopsora pachyrhizi and P. meibomiae (soybean rust) on soybeans; Phialophora spp. e.g. on vines (e.g. P. tracheiphila and P. tetraspora) and soybeans (e.g. P. gregata: stem rot); Phoma lingam (root and stem rot) on rape and cabbage and P. betae (root rot, leaf spot and damping-off) on sugar beets; Phomopsis spp. on sunflowers, vines (e.g. P. viticola: can and leaf spot) and soybeans (e.g. stem rot: P. phaseoli, teleomorph: Diaporthe phaseolorum); Physoderma maydis (brown spots) on corn; Phytophthora spp. (wilt, root, leaf, fruit and stem root) on various plants, such as paprika and cucurbits (e.g. P. capsici), soybeans (e.g. P. megasperma, syn. P. sojae), potatoes and tomatoes (e.g. P. infestans: late blight) and broad-leaved trees (e.g. P. ramorum: sudden oak death); Plasmodiophora brassicae (club root) on cabbage, rape, radish and other plants; Plasmopara spp., e.g. P. viticola (grapevine downy mildew) on vines and P. halstedii on sunflowers; Podosphaera spp. (powdery mildew) on rosaceous plants, hop, pome and soft fruits, e.g. P. leucotricha on apples; Polymyxa spp., e.g. on cereals, such as barley and wheat (P. graminis) and sugar beets (P. betae) and thereby transmitted viral diseases; Pseudocercosporella herpotrichoides (eyespot, teleomorph: Tapesia yallundae) on cereals, e.g. wheat or barley; Pseudoperonospora (downy mildew) on various plants, e.g. P. cubensis on cucurbits or P. humili on hop; Pseudopezicula tracheiphila (red fire disease or, rotbrenner', anamorph: Phialophora) on vines; Puccinia spp. (rusts) on various plants, e.g. P. triticina (brown or leaf rust), P. striiformis (stripe or yellow rust), P. hordei (dwarf rust), P. graminis (stem or black rust) or P. recondita (brown or leaf rust) on cereals, such as e.g. wheat, barley or rye, and asparagus (e.g. P. asparagi); Pyrenophora (anamorph: Drechslera) triticirepentis (tan spot) on wheat or P. teres (net blotch) on barley; Pyricularia spp., e.g. P. oryzae (teleomorph: Magnaporthe grisea, rice blast) on rice and P. grisea on turf and cereals; Pythium spp. (damping-off) on turf, rice, corn, wheat, cotton, rape, sunflowers, soybeans, sugar beets, vegetables and various other plants (e.g. P. ultimum or P. aphanidermatum); Ramularia spp., e.g. R. collo-cygni (Ramularia leaf spots, Physiological leaf spots) on barley and R. beticola on sugar beets; Rhizoctonia spp. on cotton, rice, potatoes, turf, corn, rape, potatoes, sugar beets, vegetables and various other plants, e.g. R. solani (root and stem rot) on soybeans, R. solani (sheath blight) on rice or R. cerealis (Rhizoctonia spring blight) on wheat or barley; Rhizopus stolonifer (black mold, soft rot) on strawberries, carrots, cabbage, vines and tomatoes; Rhynchosporium secalis (scald) on barley, rye and triticale; Sarocladium oryzae and S. attenuatum (sheath rot) on rice; Sclerotinia spp. (stem rot or white mold) on vegetables and field crops, such as rape, sunflowers (e.g. S. sclerotiorum) and soybeans (e.g. S. rolfsii or S. sclerotiorum); Septoria spp. on various plants, e.g. S. glycines (brown spot) on soybeans, S. tritici (Septoria blotch) on wheat and S. (syn. Stagonospora) nodorum (Stagonospora blotch) on cereals; Uncinula (syn. Erysiphe) necator(powdery mildew, anamorph: Oidium tuckeri) on vines; Setospaeria spp. (leaf blight) on corn (e.g. S. turcicum, syn. Helminthosporium turcicum) and turf; Sphacelotheca spp. (smut) on corn, (e.g. S. reiliana: head smut), sorghum and sugar cane; Sphaerotheca fulignea (powdery mildew) on cucurbits; Spongospora subterranea (powdery scab) on potatoes and thereby transmitted viral diseases; Stagonospora spp. on cereals, e.g. S. nodorum (Stagonospora blotch, teleomorph: Leptosphaeria [syn. Phaeosphaeria] nodorum) on wheat; Synchytrium endobioticum on potatoes (potato wart disease); Taphrina spp., e.g. T. deformans (leaf curl disease) on peaches and T. pruni (plum pocket) on plums; Thielaviopsis spp. (black root rot) on tobacco, pome fruits, vegetables, soybeans and cotton, e.g. T. basicola (syn. Chalara elegans); Tilletia spp. (common bunt or stinking smut) on cereals, such as e.g. T. tritici (syn. T. caries, wheat bunt) and T. controversa (dwarf bunt) on wheat; Typhula incarnata (grey snow mold) on barley or wheat; Urocystis spp., e.g. U. occulta (stem smut) on rye; Uromyces spp. (rust) on vegetables, such as beans (e.g. U. appendiculatus, syn. U. phaseoli) and sugar beets (e.g. U. betae); Ustilago spp. (loose smut) on cereals (e.g. U. nuda and U. avaenae), corn (e.g. U. maydis: corn smut) and sugar cane; Venturia spp. (scab) on apples (e.g. V. inaequalis) and pears; and Verticillium spp. (wilt) on various plants, such as fruits and ornamentals, vines, soft fruits, vegetables and field crops, e.g. V. dahliae on strawberries, rape, potatoes and tomatoes.
The compounds I, II and IV and compositions thereof, respectively, are also suitable for controlling harmful fungi in the protection of stored products or harvest and in the protection of materials. The term “protection of materials” is to be understood to denote the protection of technical and non-living materials, such as adhesives, glues, wood, paper and paperboard, textiles, leather, paint dispersions, plastics, coiling lubricants, fiber or fabrics, against the infestation and destruction by harmful microorganisms, such as fungi and bacteria. As to the protection of wood and other materials, the particular attention is paid to the following harmful fungi: Ascomycetes such as Ophiostoma spp., Ceratocystis spp., Aureobasidium pullulans, Sclerophoma spp., Chaetomium spp., Humicola spp., Petriella spp., Trichurus spp.; Basidiomycetes such as Coniophora spp., Coriolus spp., Gloeophyllum spp., Lentinus spp., Pleurotus spp., Poria spp., Serpula spp. and Tyromyces spp., Deuteromycetes such as Aspergillus spp., Cladosporium spp., Penicillium spp., Trichorma spp., Alternaria spp., Paecilomyces spp. and Zygomycetes such as Mucor spp., and in addition in the protection of stored products and harvest the following yeast fungi are worthy of note: Candida spp. and Saccharomyces cerevisae.
The compounds I, II and IV and compositions thereof, respectively, may be used for improving the health of a plant. The invention also relates to a method for improving plant health by treating a plant, its propagation material and/or the locus where the plant is growing or is to grow with an effective amount of compounds I, II and/or IV and compositions thereof, respectively.
The term “plant health” is to be understood to denote a condition of the plant and/or its products which is determined by several indicators alone or in combination with each other such as yield (e.g. increased biomass and/or increased content of valuable ingredients), plant vigor [e.g. improved plant growth and/or greener leaves (“greening effect”)], quality (e.g. improved content or composition of certain ingredients) and tolerance to abiotic and/or biotic stress. The above identified indicators for the health condition of a plant may be interdependent or may result from each other.
The compounds of formula I, II and IV can be present in different crystal modifications whose biological activity may differ. They are likewise subject matter of the present invention.
The compounds I, II and IV are employed as such or in form of compositions by treating the fungi or the plants, plant propagation materials, such as seeds, soil, surfaces, materials or rooms to be protected from fungal attack with a fungicidally effective amount of the active substances. The application can be carried out both before and after the infection of the plants, plant propagation materials, such as seeds, soil, surfaces, materials or rooms by the fungi.
Plant propagation materials may be treated with compounds I, II and/or IV as such or a composition comprising at least one compound I, II and/or IV prophylactically either at or before planting or transplanting.
The invention also relates to agrochemical compositions comprising a solvent or solid carrier and at least one compound I, II and/or IV and to the use for controlling harmful fungi.
An agrochemical composition comprises a fungicidally effective amount of a compound I, II and/or IV. The term “effective amount” denotes an amount of the composition or of the compounds I, II and/or IV, which is sufficient for controlling harmful fungi on cultivated plants or in the protection of materials and which does not result in a substantial damage to the treated plants. Such an amount can vary in a broad range and is dependent on various factors, such as the fungal species to be controlled, the treated cultivated plant or material, the climatic conditions and the specific compound I used.
The compounds I, II and IV and salts thereof can be converted into customary types of agrochemical compositions, e.g. solutions, emulsions, suspensions, dusts, powders, pastes and granules. The composition type depends on the particular intended purpose; in each case, it should ensure a fine and uniform distribution of the compound according to the invention.
Examples for composition types are suspensions (SC, OD, FS), emulsifiable concentrates (EC), emulsions (EW, EO, ES), pastes, pastilles, wettable powders or dusts (WP, SP, SS, WS, DP, DS) or granules (GR, FG, GG, MG), which can be water-soluble or wettable, as well as gel formulations for the treatment of plant propagation materials such as seeds (GF).
Usually the composition types (e.g. SC, OD, FS, EC, WG, SG, WP, SP, SS, WS, GF) are employed diluted. Composition types such as DP, DS, GR, FG, GG and MG are usually used undiluted.
The compositions are prepared in a known manner (cf. U.S. Pat. No. 3,060,084, EP-A 707 445 (for liquid concentrates), Browning: “Agglomeration”, Chemical Engineering, Dec. 4, 1967, 147-48, Perry's Chemical Engineers Handbook, 4th, Ed., McGraw-Hill, New York, 1963, pp. 8-57 et seq., WO 91/13546, U.S. Pat. No. 4,172,714, U.S. Pat. No. 4,144,050, U.S. Pat. No. 3,920,442, U.S. Pat. No. 5,180,587, U.S. Pat. No. 5,232,701, U.S. Pat. No. 5,208,030, GB 2,095,558, U.S. Pat. No. 3,299,566, Klingman: Weed Control as a Science (J. Wiley & Sons, New York, 1961), Hance et al.: Weed Control Handbook (8th, Ed., Blackwell Scientific, Oxford, 1989) and Mollet, H. and Grubemann, A.: Formulation technology (Wiley VCH Verlag, Weinheim, 2001).
The agrochemical compositions may also comprise auxiliaries which are customary in agrochemical compositions. The auxiliaries used depend on the particular application form and active substance, respectively.
Examples for suitable auxiliaries are solvents, solid carriers, dispersants or emulsifiers (such as further solubilizers, protective colloids, surfactants and adhesion agents), organic and inorganic thickeners, bactericides, anti-freezing agents, anti-foaming agents, if appropriate colorants and tackifiers or binders (e.g. for seed treatment formulations).
Suitable solvents are water, organic solvents such as mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, alcohols such as methanol, ethanol, propanol, butanol and cyclohexanol, glycols, ketones such as cyclohexanone and gamma-butyrolactone, fatty acid dimethylamides, fatty acids and fatty acid esters and strongly polar solvents, e.g. amines such as N-methylpyrrolidone.
Solid carriers are mineral earths such as silicates, silica gels, talc, kaolins, limestone, lime, chalk, bole, loess, clays, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, e.g., ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
Suitable surfactants (adjuvants, wtters, tackifiers, dispersants or emulsifiers) are alkali metal, alkaline earth metal and ammonium salts of aromatic sulfonic acids, such as ligninsoulfonic acid (Borresperse® types, Borregard, Norway) phenolsulfonic acid, naphthalenesulfonic acid (Morwet® types, Akzo Nobel, U.S.A.), dibutylnaphthalenesulfonic acid (Nekal® types, BASF, Germany), and fatty acids, alkylsulfonates, alkylarylsulfonates, alkyl sulfates, laurylether sulfates, fatty alcohol sulfates, and sulfated hexa-, hepta- and octadecanolates, sulfated fatty alcohol glycol ethers, furthermore condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxy-ethylene octylphenyl ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenyl polyglycol ethers, tributylphenyl polyglycol ether, tristearylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignin-sulfite waste liquors and proteins, denatured proteins, polysaccharides (e.g. methylcellulose), hydrophobically modified starches, polyvinyl alcohols (Mowiol® types, Clariant, Switzerland), polycarboxylates (Sokolan® types, BASF, Germany), polyalkoxylates, polyvinylamines (Lupasol® types, BASF, Germany), polyvinylpyrrolidone and the copolymers thereof.
Examples for thickeners (i.e. compounds that impart a modified flowability to compositions, i.e. high viscosity under static conditions and low viscosity during agitation) are polysaccharides and organic and anorganic clays such as Xanthan gum (Kelzan®, CP Kelco, U.S.A.), Rhodopol® 23 (Rhodia, France), Veegum® (R.T. Vanderbilt, U.S.A.) or Attaclay® (Engelhard Corp., NJ, USA).
Bactericides may be added for preservation and stabilization of the composition. Examples for suitable bactericides are those based on dichlorophene and benzylalcohol hemi formal (Proxel® from ICI or Acticide® RS from Thor Chemie and Kathon® MK from Rohm & Haas) and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones (Acticide® MBS from Thor Chemie).
Examples for suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glycerin.
Examples for anti-foaming agents are silicone emulsions (such as e.g. Silikon® SRE, Wacker, Germany or Rhodorsil®, Rhodia, France), long chain alcohols, fatty acids, salts of fatty acids, fluoroorganic compounds and mixtures thereof.
Suitable colorants are pigments of low water solubility and water-soluble dyes. Examples to be mentioned and the designations rhodamin B, C. I. pigment red 112, C. I. solvent red 1, pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1, pigment blue 80, pigment yellow 1, pigment yellow 13, pigment red 112, pigment red 48:2, pigment red 48:1, pigment red 57:1, pigment red 53:1, pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, acid red 51, acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108.
Examples for tackifiers or binders are polyvinylpyrrolidons, polyvinylacetates, polyvinyl alcohols and cellulose ethers (Tylose®, Shin-Etsu, Japan).
Powders, materials for spreading and dusts can be prepared by mixing or concomitantly grinding the compounds I and, if appropriate, further active substances, with at least one solid carrier.
Granules, e.g. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active substances to solid carriers. Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, e.g., ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
Examples for composition types are:
1. Composition Types for Dilution with Water
10 parts by weight of a compound I according to the invention are dissolved in 90 parts by weight of water or in a water-soluble solvent. As an alternative, wetting agents or other auxiliaries are added. The active substance dissolves upon dilution with water. In this way, a composition having a content of 10% by weight of active substance is obtained.
20 parts by weight of a compound I according to the invention are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, e.g. polyvinylpyrrolidone. Dilution with water gives a dispersion. The active substance content is 20% by weight.
iii) Emulsifiable Concentrates (EC)
15 parts by weight of a compound I according to the invention are dissolved in 75 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion. The composition has an active substance content of 15% by weight.
25 parts by weight of a compound I according to the invention are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifying machine (Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion. The composition has an active substance content of 25% by weight.
In an agitated ball mill, 20 parts by weight of a compound I according to the invention are comminuted with addition of 10 parts by weight of dispersants and wetting agents and 70 parts by weight of water or an organic solvent to give a fine active substance suspension. Dilution with water gives a stable suspension of the active substance. The active substance content in the composition is 20% by weight.
50 parts by weight of a compound I according to the invention are ground finely with addition of 50 parts by weight of dispersants and wetting agents and prepared as water-dispersible or water-soluble granules by means of technical appliances (e.g. extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active substance. The composition has an active substance content of 50% by weight.
vii) Water-Dispersible Powders and Water-Soluble Powders (WP, SP, SS, WS)
75 parts by weight of a compound I according to the invention are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetting agents and silica gel. Dilution with water gives a stable dispersion or solution of the active substance. The active substance content of the composition is 75% by weight.
viii) Gel (GF)
In an agitated ball mill, 20 parts by weight of a compound I according to the invention are comminuted with addition of 10 parts by weight of dispersants, 1 part by weight of a gelling agent wetters and 70 parts by weight of water or of an organic solvent to give a fine suspension of the active substance. Dilution with water gives a stable suspension of the active substance, whereby a composition with 20% (w/w) of active substance is obtained.
5 parts by weight of a compound I according to the invention are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable composition having an active substance content of 5% by weight.
0.5 parts by weight of a compound I according to the invention is ground finely and associated with 99.5 parts by weight of carriers. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted having an active substance content of 0.5% by weight.
10 parts by weight of a compound I according to the invention are dissolved in 90 parts by weight of an organic solvent, e.g. xylene. This gives a composition to be applied undiluted having an active substance content of 10% by weight.
The agrochemical compositions generally comprise between 0.01 and 95%, preferably between 0.1 and 90%, most preferably between 0.5 and 90%, by weight of active substance. The active substances are employed in a purity of from 90% to 100%, preferably from 95% to 100% (according to NMR spectrum).
Water-soluble concentrates (LS), flowable concentrates (FS), powders for dry treatment (DS), water-dispersible powders for slurry treatment (WS), water-soluble powders (SS), emulsions (ES) emulsifiable concentrates (EC) and gels (GF) are usually employed for the purposes of treatment of plant propagation materials, particularly seeds. These compositions can be applied to plant propagation materials, particularly seeds, diluted or undiluted. The compositions in question give, after two-to-tenfold dilution, active substance concentrations of from 0.01 to 60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-use preparations. Application can be carried out before or during sowing. Methods for applying or treating agrochemical compounds and compositions thereof, respectively, on to plant propagation material, especially seeds, are known in the art, and include dressing, coating, pelleting, dusting, soaking and in-furrow application methods of the propagation material. In a preferred embodiment, the compounds or the compositions thereof, respectively, are applied on to the plant propagation material by a method such that germination is not induced, e.g. by seed dressing, pelleting, coating and dusting.
In a preferred embodiment, a suspension-type (FS) composition is used for seed treatment. Typically, a FS composition may comprise 1-800 g/l of active substance, 1-200 g/l Surfactant, 0 to 200 g/l antifreezing agent, 0 to 400 g/l of binder, 0 to 200 g/l of a pigment and up to 1 liter of a solvent, preferably water.
The active substances can be used as such or in the form of their compositions, e.g. in the form of directly sprayable solutions, powders, suspensions, dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading, brushing, immersing or pouring. The application forms depend entirely on the intended purposes; it is intended to ensure in each case the finest possible distribution of the active substances according to the invention.
Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. Alternatively, it is possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.
The active substance concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.001 to 1% by weight of active substance.
The active substances may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply compositions comprising over 95% by weight of active substance, or even to apply the active substance without additives.
When employed in plant protection, the amounts of active substances applied are, depending on the kind of effect desired, from 0.001 to 2 kg per ha, preferably from 0.005 to 2 kg per ha, more preferably from 0.05 to 0.9 kg per ha, in particular from 0.1 to 0.75 kg per ha.
In treatment of plant propagation materials such as seeds, e.g. by dusting, coating or drenching seed, amounts of active substance of from 0.1 to 1000 g, preferably from 1 to 1000 g, more preferably from 1 to 100 g and most preferably from 5 to 100 g, per 100 kilogram of plant propagation material (preferably seed) are generally required.
When used in the protection of materials or stored products, the amount of active substance applied depends on the kind of application area and on the desired effect. Amounts customarily applied in the protection of materials are, e.g., 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active substance per cubic meter of treated material.
Various types of oils, wetters, adjuvants, herbicides, bactericides, other fungicides and/or pesticides may be added to the active substances or the compositions comprising them, if appropriate not until immediately prior to use (tank mix). These agents can be admixed with the compositions according to the invention in a weight ratio of 1:100 to 100:1, preferably 1:10 to 10:1.
Adjuvants which can be used are in particular organic modified polysiloxanes such as Break Thru S 240®; alcohol alkoxylates such as Atplus 245®, Atplus MBA 1303®, Plurafac LF 300® and Lutensol ON 30®; EO/PO block polymers, e.g. Pluronic RPE 2035® and Genapol B®; alcohol ethoxylates such as Lutensol XP 80®; and dioctyl sulfosuccinate sodium such as Leophen RA®.
The compositions according to the invention can, in the use form as fungicides, also be present together with other active substances, e.g. with herbicides, insecticides, growth regulators, fungicides or else with fertilizers, as pre-mix or, if appropriate, not until immediately prior to use (tank mix).
Mixing the compounds I, II and/or IV or the compositions comprising them in the use form as fungicides with other fungicides results in many cases in an expansion of the fungicidal spectrum of activity being obtained or in a prevention of fungicide resistance development. Furthermore, in many cases, synergistic effects are obtained.
The following list of active substances, in conjunction with which the compounds according to the invention can be used, is intended to illustrate the possible combinations but does not limit them:
A) strobilurins
The present invention furthermore relates to agrochemical compositions comprising a mixture of at least one compound I, II and/or IV (component 1) and at least one further active substance useful for plant protection, e.g. selected from the groups A) to I) (component 2), in particular one further fungicide, e.g. one or more fungicide from the groups A) to F), as described above, and if desired one suitable solvent or solid carrier. Those mixtures are of particular interest, since many of them at the same application rate show higher efficiencies against harmful fungi. Furthermore, combating harmful fungi with a mixture of compounds I, II and/or IV and at least one fungicide from groups A) to F), as described above, is more efficient than combating those fungi with individual compounds I, II or IV or individual fungicides from groups A) to F). By applying compounds I, II and/or IV together with at least one active substance from groups A) to I) a synergistic effect can be obtained, i.e. more then simple addition of the individual effects is obtained (synergistic mixtures).
According to this invention, applying the compounds I, II and/or IV together with at least one further active substance is to be understood to denote that at least one compound of formula I, II and/or IV and at least one further active substance occur simultaneously at the site of action (i.e. the harmful fungi to be controlled or their habitats such as infected plants, plant propagation materials, particularly seeds, surfaces, materials or the soil as well as plants, plant propagation materials, particularly seeds, soil, surfaces, materials or rooms to be protected from fungal attack) in a fungicidally effective amount. This can be obtained by applying the compounds I, II and/or IV and at least one further active substance simultaneously, either jointly (e.g. as tank-mix) or separately, or in succession, wherein the time interval between the individual applications is selected to ensure that the active substance applied first still occurs at the site of action in a sufficient amount at the time of application of the further active substance(s). The order of application is not essential for working of the present invention.
In binary mixtures, i.e. compositions according to the invention comprising one compound I, II or IV (component 1) and one further active substance (component 2), e.g. one active substance from groups A) to I), the weight ratio of component 1 and component 2 generally depends from the properties of the active substances used, usually it is in the range of from 1:100 to 100:1, regularly in the range of from 1:50 to 50:1, preferably in the range of from 1:20 to 20:1, more preferably in the range of from 1:10 to 10:1 and in particular in the range of from 1:3 to 3:1.
In ternary mixtures, i.e. compositions according to the invention comprising one compound I (component 1) and a first further active substance (component 2) and a second further active substance (component 3), e.g. two active substances from groups A) to I), the weight ratio of component 1 and component 2 depends from the properties of the active substances used, preferably it is in the range of from 1:50 to 50:1 and particularly in the range of from 1:10 to 10:1, and the weight ratio of component 1 and component 3 preferably is in the range of from 1:50 to 50:1 and particularly in the range of from 1:10 to 10:1.
The components can be used individually or already partially or completely mixed with one another to prepare the composition according to the invention. It is also possible for them to be packaged and used further as combination composition such as a kit of parts.
In one embodiment of the invention, the kits may include one or more, including all, components that may be used to prepare a subject agrochemical composition. E.g., kits may include one or more fungicide component(s) and/or an adjuvant component and/or an insecticide component and/or a growth regulator component and/or a herbicide. One or more of the components may already be combined together or preformulated. In those embodiments where more than two components are provided in a kit, the components may already be combined together and as such are packaged in a single container such as a vial, bottle, can, pouch, bag or canister. In other embodiments, two or more components of a kit may be packaged separately, i.e., not preformulated. As such, kits may include one or more separate containers such as vials, cans, bottles, pouches, bags or canisters, each container containing a separate component for an agrochemical composition. In both forms, a component of the kit may be applied separately from or together with the further components or as a component of a combination composition according to the invention for preparing the composition according to the invention.
The user applies the composition according to the invention usually from a predosage device, a knapsack sprayer, a spray tank or a spray plane. Here, the agrochemical composition is made up with water and/or buffer to the desired application concentration, it being possible, if appropriate, to add further auxiliaries, and the ready-to-use spray liquor or the agrochemical composition according to the invention is thus obtained. Usually, 50 to 500 liters of the ready-to-use spray liquor are applied per hectare of agricultural useful area, preferably 100 to 400 liters.
According to one embodiment, individual components of the composition according to the invention such as parts of a kit or parts of a binary or ternary mixture may be mixed by the user himself in a spray tank and further auxiliaries may be added, if appropriate (tank mix).
In a further embodiment, either individual components of the composition according to the invention or partially premixed components, e.g. components comprising compounds I, II and/or IV and/or active substances from the groups A) to I), may be mixed by the user in a spray tank and further auxiliaries and additives may be added, if appropriate (tank mix).
In a further embodiment, either individual components of the composition according to the invention or partially premixed components, e.g. components comprising compounds I, II and/or IV and/or active substances from the groups A) to I), can be applied jointly (e.g. after tankmix) or consecutively.
Preference is also given to mixtures comprising a compound I, II and/or IV (component 1) and at least one active substance selected from the strobilurines of group A) (component 2) and particularly selected from azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, orysastrobin, picoxystrobin, pyraclostrobin and trifloxystrobin.
Preference is also given to mixtures comprising a compound I, II and/or IV (component 1) and at least one active substance selected from the carboxamides of group B) (component 2) and particularly selected from bixafen, boscalid, sedaxane, fenhexamid, metalaxyl, isopyrazam, mefenoxam, ofurace, dimethomorph, flumorph, fluopicolid (picobenzamid), zoxamide, carpropamid, mandipropamid and N-(3′,4′,5′-trifluorobiphenyl-2-yl)-3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxamide.
Preference is given to mixtures comprising a compound of formula I, II and/or IV (component 1) and at least one active substance selected from the azoles of group C) (component 2) and particularly selected from cyproconazole, difenoconazole, epoxiconazole, fluquinconazole, flusilazole, flutriafol, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, cyazofamid, benomyl, carbendazim and ethaboxam.
Preference is also given to mixtures comprising a compound I, II and/or IV (component 1) and at least one active substance selected from the heterocyclic compounds of group D) (component 2) and particularly selected from fluazinam, cyprodinil, fenarimol, mepanipyrim, pyrimethanil, triforine, fludioxonil, dodemorph, fenpropimorph, tridemorph, fenpropidin, iprodione, vinclozolin, famoxadone, fenamidone, probenazole, proquinazid, acibenzolar-S-methyl, captafol, folpet, fenoxanil, quinoxyfen and 5-ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidine-7-ylamine.
Preference is also given to mixtures comprising a compound I, II and/or IV (component 1) and at least one active substance selected from the carbamates of group E) (component 2) and particularly selected from mancozeb, metiram, propineb, thiram, iprovalicarb, benthiavalicarb and propamocarb.
Preference is also given to mixtures comprising a compound I, II and/or IV (component 1) and at least one active substance selected from the fungicides given in group F) (component 2) and particularly selected from dithianon, fentin salts, such as fentin acetate, fosetyl, fosetyl-aluminium, H3PO3 and salts thereof, chlorthalonil, dichlofluanid, thiophanat-methyl, copper acetate, copper hydroxide, copper oxychloride, copper sulfate, sulfur, cymoxanil, metrafenone and spiroxamine.
Accordingly, the present invention furthermore relates to compositions comprising one compound I, II and/or IV (component 1) and one further active substance (component 2), which further active substance is selected from the column “Component 2” of the lines B-1 to B-346 of Table B.
A further embodiment relates to the compositions B-1 to B-346 listed in Table B, where a row of Table B corresponds in each case to a fungicidal composition comprising one of the in the present specification individualized compounds of formula I or II (component 1) and the respective further active substance from groups A) to I) (component 2) stated in the row in question. Preferably, the compositions described comprise the active substances in synergistically effective amounts.
The active substances referred to as component 2, their preparation and their activity against harmful fungi is known (cf.: http://www.alanwood.net/pesticides/); these substances are commercially available. The compounds described by IUPAC nomenclature, their preparation and their fungicidal activity are also known (cf. Can. J. Plant Sci. 48(6), 587-94, 1968; EP-A 141 317; EP-A 152 031; EP-A 226 917; EP-A 243 970; EP-A 256 503; EP-A 428 941; EP-A 532 022; EP-A 1 028 125; EP-A 1 035 122; EP-A 1 201 648; EP-A 1 122 244, JP 2002316902; DE 19650197; DE 10021412; DE 102005009458; U.S. Pat. No. 3,296,272; U.S. Pat. No. 3,325,503; WO 98/46608; WO 99/14187; WO 99/24413; WO 99/27783; WO 00/29404; WO 00/46148; WO 00/65913; WO 01/54501; WO 01/56358; WO 02/22583; WO 02/40431; WO 03/10149; WO 03/11853; WO 03/14103; WO 03/16286; WO 03/53145; WO 03/61388; WO 03/66609; WO 03/74491; WO 04/49804; WO 04/83193; WO 05/120234; WO 05/123689; WO 05/123690; WO 05/63721; WO 05/87772; WO 05/87773; WO 06/15866; WO 06/87325; WO 06/87343; WO 07/82098; WO 07/90624).
The mixtures of active substances can be prepared as compositions comprising besides the active ingredients at least one inert ingredient by usual means, e.g. by the means given for the compositions of compounds I, II and/or IV.
Concerning usual ingredients of such compositions reference is made to the explanations given for the compositions containing compounds I, II and/or IV.
The mixtures of active substances according to the present invention are suitable as fungicides, as are the compounds of formula I, II ad IV. They are distinguished by an outstanding effectiveness against a broad spectrum of phytopathogenic fungi, especially from the classes of the Ascomycetes, Basidiomycetes, Deuteromycetes and Peronosporomycetes (syn. Oomycetes). In addition, it is referred to the explanations regarding the fungicidal activity of the compounds and the compositions containing compounds I, II and/or IV respectively.
The compounds I, II and IV and pharmaceutically acceptable salts thereof are also suitable for treating diseases in men and animals, especially as antimycotics, for treating cancer and for treating virus infections. The term “antimycotic”, as distinguished from the term “fungicide”, refers to a medicament for combating zoopathogenic or humanpathogenic fungi, i.e. for combating fungi in animals, especially in mammals (including humans) and birds.
Thus, a further aspect of the present invention relates to a medicament comprising at least one compound of the formulae I, II and/or IV and/or at least one pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.
Suitable pharmaceutically acceptable salts are especially physiologically tolerated salts of the compound I, in particular the acid addition salts with physiologically acceptable acids. Examples of suitable organic and inorganic acids are hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid, C1-C4-alkylsulfonic acids, such as methanesulfonic acid, aromatic sulfonic acids, such as benzenesulfonic acid and toluenesulfonic acid, oxalic acid, maleic acid, fumaric acid, lactic acid, tartaric acid, adipic acid and benzoic acid. Further suitable acids are described, for example, in Fortschritte der Arzneimittelforschung, Volume 10, pages 224 ff., Birkhäuser Verlag, Basle and Stuttgart, 1966, the entire contents of which is expressly incorporated herein by way of reference.
Suitable carriers are, for example, solvents, carriers, excipients, binders and the like customarily used for pharmaceutical formulations, which are described below in an exemplary manner for individual types of administration.
A further aspect of the present invention relates to the use of compounds I, II and IV or of pharmaceutically acceptable salts thereof for preparing an antimycotic medicament; i.e. for preparing a medicament for the treatment and/or prophylaxis of infections with humanpathogenic and/or zoopathogenic fungi. Another aspect of the present invention relates to the use of compounds of formulae I, II and/or IV or of pharmaceutically acceptable salts thereof for preparing a medicament for the treatment of cancer. Another aspect of the present invention relates to the use of compounds of formulae I, II and/or IV or of pharmaceutically acceptable salts thereof for preparing a medicament for the treatment or prophylaxis of virus infections.
The compounds of formulae I, II and IV and/or their pharmaceutically acceptable salts are suitable for the treatment, inhibition or control of growth and/or propagation of tumor cells and the disorders associated therewith. Accordingly, they are suitable for cancer therapy in warm-blooded vertebrates, for example mammals and birds, in particular man, but also other mammals, in particular useful and domestic animals, such as dogs, cats, pigs, ruminants (cattle, sheep, goats, bison, etc.), horses and birds, such as chicken, turkey, ducks, geese, guineafowl and the like.
The compounds of formulae I, II and IV and/or their pharmaceutically acceptable salts are suitable for the therapy of cancer or cancerous disorders of the following organs: breast, lung, intestine, prostate, skin (melanoma), kidney, bladder, mouth, larynx, oesophagus, stomach, ovaries, pancreas, liver and brain or CNS.
The compounds of formulae I, II and IV and/or their pharmaceutically acceptable salts are suitable for the treatment of virus infections in warm-blooded vertebrates, for example mammals and birds, in particular man, but also other mammals, in particular useful and domestic animals, such as dogs, cats, pigs, ruminants (cattle, sheep, goats, bison, etc.), horses and birds, such as chicken, turkey, ducks, geese, guineafowl and the like. They are suitable for treating virus infections like retrovirus infections such as HIV and HTLV, influenza virus infection, rhinovirus infections, herpes and the like.
The compounds according to the invention can be administered in a customary manner, for example orally, intravenously, intramuscularly or subcutaneously. For oral administration, the active compound can be mixed, for example, with an inert diluent or with an edible carrier; it can be embedded into a hard or soft gelatin capsule, it can be compressed to tablets or it can be mixed directly with the food/feed. The active compound can be mixed with excipients and administered in the form of indigestible tablets, buccal tablets, pastilles, pills, capsules, suspensions, potions, syrups and the like. Such preparations should contain at least 0.1% of active compound. The composition of the preparation may, of course, vary. It usually comprises from 2 to 60% by weight of active compound, based on the total weight of the preparation in question (dosage unit). Preferred preparations of the compound I according to the invention comprise from 10 to 1000 mg of active compound per oral dosage unit.
The tablets, pastilles, pills, capsules and the like may furthermore comprise the following components: binders, such as traganth, gum arabic, corn starch or gelatin, excipients, such as dicalcium phosphate, disintegrants, such as corn starch, potato starch, alginic acid and the like, glidants, such as magnesium stearate, sweeteners, such as sucrose, lactose or saccharin, and/or flavors, such as peppermint, vanilla and the like.
Capsules may furthermore comprise a liquid carrier. Other substances which modify the properties of the dosage unit may also be used. For example, tablets, pills and capsules may be coated with schellack, sugar or mixtures thereof. In addition to the active compound, syrups or potions may also comprise sugar (or other sweeteners), methyl- or propylparaben as preservative, a colorant and/or a flavor. The components of the active compound preparations must, of course, be pharmaceutically pure and nontoxic at the quantities employed. Furthermore, the active compounds can be formulated as preparations with a controlled release of active compound, for example as delayed-release preparations.
The active compounds can also be administered parenterally or intraperitoneally. Solutions or suspensions of the active compounds or their salts can be prepared with water using suitable wetting agents, such as hydroxypropylcellulose. Dispersions can also be prepared using glycerol, liquid polyethylene glycols and mixtures thereof in oils. Frequently, these preparations furthermore comprise a preservative to prevent the growth of microorganisms.
Preparations intended for injections comprise sterile aqueous solutions and dispersions and also sterile powders for preparing sterile solutions and dispersions. The preparation has to be sufficiently liquid for injection. It has to be stable under the preparation and storage conditions and it has to be protected against contamination by microorganisms. The carrier may be a solvent or a dispersion medium, for example, water, ethanol, a polyol (for example glycerol, propylene glycol or liquid polyethylene glycol), a mixture thereof and/or a vegetable oil.
The invention is further illustrated by the following, non-limiting examples.
Proton and carbon NMR spectra were obtained on a Bruker AC 300 spectrometer at 300 MHz. Proton spectra were referenced to tetramethylsilane as an internal standard and the carbon spectra were referenced to CDCl3 (purchased from Aldrich or Cambridge Isotope Laboratories, unless otherwise specified). Melting points were obtained on a MeI-Temp II apparatus and are uncorrected. ESI Mass spectra were obtained on a Shimadzu LCMS-2010 EV Mass Spectrometer. HPLC analyses were obtained using an Alltech Alltima C18 Rocket Column utilizing PDA detection at 254 nm (unless otherwise specified) on a Shimadzu Prominence HPLC system. The following time program was utilized (flow rate of 2.5 mL per minute):
The title compound was prepared in analogy to the method described in DE-A-2830120.
In a round-bottomed flask, magnesium (0.59 g, 24.24 mmol) was placed under a nitrogen atmosphere and 1 ml of a solution of 1-(4-bromo-2-methyl-butyl)-2-chlorobenzene (6.00 g, 24.24 mmol) in diethylether (15 ml) was added. After initiation of the reaction, the remaining bromide solution was added dropwise at such a rate that the reaction mixture kept refluxing. Upon completion of the addition, the mixture was refluxed for another 1.5 h and then cooled to 0° C. LiCl (0.103 g, 2.42 mmol) and CuCl (0.163 g, 1.21 mmol) were added at this temperature, followed by the addition of pivaline aldehyde (2.09 g, 24.24 mmol) in diethylether (10 ml). Subsequently, the reaction mixture was warmed to room temperature and stirred for 16 h. The mixture was then poured on ice water (50 ml), acidified with sulfuric acid and extracted with methyl tert-butyl ether (MTBE) (3×100 ml). The combined organic phases were washed with saturated brine, dried (Na2SO4) and the solvent was removed in vacuo. Column chromatography (silica gel, cyclohexane/ethyl acetate) yielded the product as a mixture of two diasteromers in a ratio of 1:1 in form of a light yellow oil (2.46 g, 40.0%).
1H-NMR (500 MHz, CDCl3): 7.30 (s, 2H), 7.20-7.08 (m, 6H), 3.35 (d, 1H), 3.30 (d, 1H), 2.98 (d, 1H), 2.72 (m, 1H), 2.58 (m, 1H), 2.30 (dd, 1H), 2.05 (broad s, 2H), 1.60-1.31 (m, 6H), 0.88 (m, 22H).
Oxalyl chloride (0.872 g, 6.87 mmol) was dissolved in dichloromethane (20 ml) and cooled to −70° C. A mixture of dimethylsulfoxide (DMSO, 0.975 ml) in dichloromethane (20 ml) was added at this temperature and the resulting mixture was stirred for 5 min at the same temperature. A solution of 6-(2-chlorophenyl)-2,2,5-trimethyl-hexan-3-ol (1.400 g, 5.50 mmol) in dichloromethane (20 ml) was added dropwise, the resulting mixture was stirred for 5 min and then the reaction was stopped by the addition of triethylamine (3.80 ml, 27.47 mmol). After warming to room temperature, aqueous ammonium chloride (20 ml) was added and the mixture was extracted with dichloromethane (3×100 ml). The combined organic phases were washed with water, dried (Na2SO4) and the solvent was distilled off. The title product was obtained in form of a brown oil (0.99 g, 71%) and was used in the next reaction step without further purification.
1H-NMR (500 MHz, CDCl3): 7.35-7.30 (d, 1H), 7.21-7.08 (m, 3H), 2.78-2.60 (m, 2H), 2.40 (m, 3H), 1.10 (s, 9H), 0.88 (d, 3H).
Sodium hydride (0.119 g, 4.70 mmol) was placed in a mixture of tetrahydrofuran (10 ml) and DMSO (15 ml) under nitrogen. Trimethylsulfoniumiodide (0.959 g, 4.70 mmol) in DMSO (10 ml) was added at 5° C. and the resulting mixture was stirred for 10 min at this temperature. Subsequently, a solution of 6-(2-chlorophenyl)-2,2,5-trimethyl-hexan-3-one (0.99 g, 3.92 mmol) in DMSO (5 ml) was added dropwise over 10 min and the mixture was allowed to warm up to room temperature and was stirred for another 16 h. Aqueous ammonium chloride (20 ml) was then added and the aqueous phase was extracted with MTBE (3×100 ml). The combined organic phases were washed with water, dried (Na2SO4) and the solvent was distilled off. The product was obtained as a mixture of two diasteromers in a ratio of 2:1 in form of a brown oil and was used in the next reaction step without further purification.
1H-NMR (500 MHz, CDCl3): 7.32-7.27 (m, 2H), 7.20-7.03 (m, 6H), 3.83 (dd, 1H), 2.90-2.48 (m, 6H), 1.96-1.12 (m, 7H), 1.10 (d, 3H), 1.01-0.90 (m, 21H).
To sodium hydride (0.099 g, 3.94 mmol) placed in DMF (15 ml) under nitrogen, a solution of 1,2,4-1H-triazole (0.272 g, 3.94 mmol) in DMF (3 ml) was added at a temperature below 30° C. The resulting mixture was stirred at room temperature for 1 h until a clear solution was obtained. 2-tert-Butyl-2-[3-(2-chlorophenyl)-2-methyl-propyl]-oxirane (1.00 g, 3.75 mmol) in DMF (3 ml) was added and the reaction mixture was stirred at 130° C. for 16 h. After cooling to room temperature, the mixture was poured onto hydrochloric acid (15 ml, 10% solution). The mixture was then extracted with MTBE (3×60 ml), the combined organic phases were dried (Na2SO4) and the solvent was removed. Column chromatography (silica gel, cyclohexane/ethyl acetate) yielded the product as a mixture of two diasteromers in a ratio of 2:1 in form of a brown oil (0.45 g, 36%).
1H-NMR (500 MHz, CDCl3): 8.18 and 7.98 (s, 1H), 7.97 (s, 1H), 7.36-7.24 (m, 1H), 7.18-7.05 (m, 2H), 7.02-7.00 (m, 1H), 4.20 (dt, 2H), 3.24 und 3.18 (broad s, 1H), 2.42 and 2.23 (m, 2H), 1.81-1.22 (m, 3H), 0.96 (s, 9H), 0.96 und 0.79 (d, 3H).
To 6-(2-chlorophenyl)-2,2,5-trimethyl-3-[1,2,4]triazol-1-ylmethyl-hexan-3-ol (0.20 g, 0.60 mmol) dissolved in NMP (3 ml), sulfur (0.191 g, 5.96 mmol) was added and the mixture was stirred at 160° C. for 16 h. The mixture was diluted with MTBE and the unsoluble components were filtered off. The organic phase was washed with water, dried (Na2SO4) and the solvent was removed. Column chromatography (silica gel, cyclohexane/ethyl acetate) yielded the product as a diasteromeric mixture in form of a brown oil (0.202 g, 92%).
1H-NMR (500 MHz, CDCl3): 7.81 and 7.77 (s, 1H), 7.29-7.02 (m, 4H), 4.39 and 4.30 (s, 2H), 3.10-2.19 (m, 2H), 1.80-1.55 (m, 3H), 1.22 (m, 1H), 1.00 and 0.99 (s, 9H), 0.90 and 0.62 (d, 3H).
The following compounds were prepared analogously.
Log P=3.80
HPLC/MS: 344 (−18); 3.821 min
HPLC/MS: 350 (−18); 4.004 min
HPLC/MS: 352; 3.617 min
HPLC/MS: 350 (−18); 4.016 min
HPLC/MS: 330 (−18); 3.953 min
HPLC/MS: 402; 4.003 min
To a suspension of lithium aluminium hydride (20.26 g, 37.95 mmol) in THF (tetrahydrofuran) (300 mL) under nitrogen atmosphere was slowly added a solution of 3-(4-chloro-phenyl)-acrylic acid (65.00 g, 355.96 mmol) in THF (500 mL) under cooling with an ice bath. The resulting mixture was stirred until it reached room temperature and then refluxed for 12 h. After cooling to room temperature, a 10% HCl solution was added at 0° C. and the resultant solution was stirred for 0.5 h. The mixture was then extracted with MTBE (methyl tert-butyl ether) and the organic layers were washed with water, dried and evaporated. The title compound was obtained as a brown oil (70.0 g, 98%).
3-(4-Chloro-phenyl)-propan-1-ol of step 9.1 (59.0 g, 170 mmol) was added to a solution of 47% aqueous HBr (295 mL) and the resulting mixture was stirred at room temperature for 2 h. Water was added and the mixture was extracted with CH2Cl2. The combined organic phases were washed with water, dried and evaporated. The crude residue was purified by flash chromatography on silica gel to give the title compound as a brown oil (28.1 g, 35%).
To a suspension of magnesium turnings (1.551 g, 63.81 mmol) in THF (20 mL) was added dropwise a solution of 1-(3-bromo-propyl)-4-chloro-benzene of step 9.2 (15.00 g, 64.23 mmol) in diethyl ether (30 mL) under nitrogen atmosphere. The reaction was activated by adding one drop of bromine and the refluxed mixture was stirred for 2 h. After cooling the reaction to 0° C., a solution of LiCl (0.270 g, 6.38 mmol) and CuCl2 (0.429 g, 3.19 mmol) in THF (20 mL) was added dropwise followed by a solution of pivaloyl aldehyde (5.496 g, 63.81 mmol) in diethyl ether (20 mL). The reaction was allowed to reach room temperature and was stirred for 12 h. Iced water was added and the mixture was acidified with sulphuric acid. After extraction with MTBE, the combined organic phases were washed with water, dried and evaporated. The crude residue was purified by flash chromatography on silica gel to give the title compound as a brown oil (4.30 g, 28%).
To a solution of oxalyl chloride (2.833 g, 22.32 mmol) in 20 ml of CH2Cl2 was added DMSO (dimethylsulfoxide) (3.489 g, 44.65 mmol) in 20 ml of CH2Cl2 at −70° C. The resulting mixture was stirred for 5 min and then 6-(4-chloro-phenyl)-2,2-dimethyl-hexan-3-ol of step 9.3 (4.30 g, 17.86 mmol) dissolved in 20 ml of CH2Cl2 was added dropwise. After stirring for 2 h at −70° C., triethylamine (9.036 g, 89.30 mmol) was added. The reaction mixture was then allowed to reach room temperature and was stirred for 12 h. After quenching with a solution of 10% aqueous HCl, the mixture was extracted with CH2Cl2. The combined organic phases were washed with 10% aqueous HCl and water, dried and evaporated. The crude residue was purified by flash chromatography on silica gel to give the title compound as a brown oil (4.20 g, 98%).
To a suspension of NaH (1.058 g, 41.88 mmol) in 50 mL of THF was added under nitrogen atmosphere 40 mL of DMSO. At 5° C., a solution of trimethylsulfonium iodide was added dropwise and the resulting mixture was stirred for 1 h. A solution of 6-(4-chloro-phenyl)-2,2-dimethyl-hexan-3-one of step 9.4 (4.00 g, 16.75 mmol) in DMSO (40 mL) was then slowly added and the reaction was stirred at room temperature for 12 h. After quenching with a saturated solution of aqueous ammonium chloride, the mixture was extracted with MTBE. The combined organics were washed with water, dried and evaporated, to give the title compound as a brown oil (4.10 g, 97%).
To a solution of 2-tert-butyl-2-[3-(2-chloro-phenyl)-propyl]-oxirane of step 9.5 (4.10 g, 16.22 mmol) in ethanol (5 mL) was added KOH (1.82 g, 32.44 mmol) and 1H-1,2,4-triazole (1.45 g, 21.09 mmol). The resulting mixture was refluxed and stirred for 12 h. After cooling to room temperature, the reaction mixture was directly purified by flash chromatography on silica gel to give the title compound as a brown oil (2.14 g, 37%).
To a solution of 6-(4-chloro-phenyl)-2,2-dimethyl-3-[1,2,4]triazol-1-ylmethyl-hexan-3-ol of step 9.6 (0.700 g, 2.17 mmol) in NMP (N-methylpyrrolidone) (8 mL) was added sulphur (0.696 g, 21.75 mmol). The reaction was stirred at 160° C. for 12 h, then diluted with MTBE and filtrated. The resulting filtrate was washed with a solution of 10% aqueous HCl and water, dried and evaporated. The crude residue was purified by flash chromatography on silica gel to give the title compound as a brown oil (0.434 g, 57%).
HPLC/MS: 336 (−18); 3.437 min
The following compounds were prepared analogously.
Log P: 3.30
HPLC/MS: 338 (−18); 3.257 min
HPLC/MS: 320 (−18); 3.474 min
HPLC/MS: 388; 3.934 min
HPLC/MS: 316 (−18); 3.637 min
A solution of CuBr (530 mg, 3.75 mmol) and 1,4-dibromobutane (8.98 mL, 75.26 mmol) in HMPA (15 mL) was added to a solution of 4-fluorophenyl magnesium bromide (75.25 mmol) in THF (180 mL) at room temperature. The reaction mixture was refluxed for 4 h (reaction progress was monitored by GC). The mixture was quenched by NH4Cl (sat. aq., 100 mL) and extracted with EtOAc (ethylacetate) (3×200 mL). The organic phases were washed with brine (100 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by column chromatography (silica gel, heptane) to afford the title compound (11.6 g, 67%) as clear oil.
To a suspension of magnesium turnings (1.24 g, 51.7 mmol) and a small crystal of iodine in anhydrous THF (20 mL) was added solution of 4-(4-fluorophenyl)-bromobutane of step 15.1 (11.6 g, 50.2 mmol) in anhydrous THF (20 mL). The mixture was heated to initiate the reaction and kept at reflux for 1 h. The mixture was cooled to 0° C., and a solution of pivalaldehyde (4.32 g, 50.2 mmol) in anhydrous THF (10 mL) was added dropwise. The reaction mixture was stirred at room temperature for 4 h, quenched by NH4Cl (sat. aq., 100 mL) and extracted with EtOAc (3×200 mL). The organic phases were washed with brine (100 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by column chromatography (silica gel, eluents: hexanes/EtOAc 4:1) to afford the title compound (2.2 g, 18%) as clear oil.
To a stirred solution of 7-(4-fluorophenyl)-2,2-dimethylheptan-3-ol of step 15.2 (2.2 g, 9.23 mmol) in anhydrous CH2Cl2 (30 mL) was added molecular sieves (4A, powdered, 2.2 g). The mixture was cooled to 0° C. and pyridium chlorochromate (2.99 g, 13.84 mmol) was added in one portion. The reaction mixture was stirred at room temperature for 6 h, diluted with diethyl ether (60 mL) and filtered through celite plug. The filtrate was dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by column chromatography (silica gel, eluents: hexanes/EtOAc 4:1) to afford the title compound (2.0 g, 91%) as clear oil.
A solution of dimethyl sulfide (1.69 mL, 23.04 mmol) in acetonitrile (5 mL) was added to a stirred and chilled (0° C.) solution of dimethyl sulfate (2.0 mL, 20.95 mmol) in acetonitrile (5 mL). The reaction mixture was warmed to room temperature and stirred for 16 h. At this time, 7-(4-fluorophenyl)-2,2-dimethylheptan-3-one of step 15.3 (1.65 g, 6.98 mmol) in DMSO (7 mL) was added, followed by addition of powdered KOH (1.95 g, 24.90 mmol). The reaction mixture was stirred at room temperature for an additional 16 h. At this time, the reaction mixture was diluted with water (30 mL) and extracted with EtOAc (3×50 mL). The combined organic phases were dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the crude product as a light-yellow oil. The crude product was used directly in the next step without further purification. Yield: 1.7 g (crude)
A solution of triazole (730 mg, 10.2 mmol) in DMF (5 mL) was added to a stirred and chilled suspension of NaH (0.406 g, 10.193 mmol) in DMF (dimethylformamide) (20 ml). After stirring at 0° C. for 1 h, the reaction mixture was warmed to room temperature and stirred for an additional 1 h. A solution of 2-tert-butyl-2-[4-(4-fluorophenyl)butyl]oxirane of step 15.4 (1.7 g, crude) in DMF (5 mL) was added at r.t. and the reaction mixture was heated at 80° C. for about 12 h. After this time the reaction mixture was poured into ice cold water (50 mL) and extracted with EtOAc (3×50 mL). The combined organic extracts were dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel, eluent: hexanes:EtOAc 3:1) afford the title compound (820 mg, 37% over two steps) as light yellow gum.
To a solution of the triazole compound of step 15.5 (600 mg, 1.88 mmol) in DMF (20 ml), S8 (901 mg, 28.2 mmol) was added in one portion. The mixture was heated to reflux for 48 hours. The reaction was quenched with brine (20 ml) and extracted with EtOAc (3×20 mL). The organic phases were washed with brine (100 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by column chromatography with EtOAc/hexanes (1:9 to 2:3) as eluents to afford 250 mg of the title compound as brown solid, yield 38%).
Log P=3.70
The following compounds were prepared analogously.
Log P=3.60
Log P=4.20
Log P=4.00
Log P=3.40
Log P=4.70
Log P=4.00
Log P=4.20
Log P=4.40
The fungicidal action of the compounds of the formulae I and II was demonstrated by the following experiments:
The spray solutions were prepared in several steps: The stock solutions were prepared by adding a mixture of acetone and/or dimethylsulfoxide and the wetting agent/emulsifier Wettol, which is based on ethoxylated alkylphenoles, in a relation (volume) solvent-emulsifier of 99 to 1 to 25 mg of the compound to give a total of 10 ml. Water was then added to total volume of 100 ml. This stock solution was diluted with the described solvent-emulsifier-water mixture to the given concentration.
1. Preventative Control of Brown Rust on Wheat Caused by Puccinia recondite
The first two developed leaves of pot-grown wheat seedling were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture as described below. The next day the plants were inoculated with spores of Puccinia recondita. To ensure the success the artificial inoculation, the plants were transferred to a humid chamber without light and a relative humidity of 95 to 99% and 20 to 24° C. for 24 h. Then the trial plants were cultivated for 6 days in a greenhouse chamber at 20-24° C. and a relative humidity between 65 and 70%. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area. The plants which had been treated with an aqueous active compound preparation comprising 300 ppm of the active compounds of examples 2, 5, 6, 8, 9, 16, 18 and 20 showed an infection of at most 20%, whereas the untreated plants were 70% infected.
2. Control of Late Blight on Tomatoes Caused by Phytophthora infestans
Young seedlings of tomato plants were grown in pots. These plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture mentioned in the table below. The next day, the treated plants were inoculated with an aqueous suspension of sporangia of Phytophthora infestans. After inoculation, the trial plants were immediately transferred to a humid chamber. After 6 days at 18 to 20° C. and a relative humidity close to 100% the extent of fungal attack on the leaves was visually assessed as % diseased leaf area. The plants which had been treated with an aqueous active compound preparation comprising 300 ppm of the active compounds of examples 7, 15 and 17 showed an infection of at most 20%, whereas the untreated plants were 90% infected.
3. Curative Control of Soy Bean Rust on Soy Beans Caused by Phakopsora pachyrhizi
Leaves of pot-grown soy bean seedlings were inoculated with spores of Phakopsora pachyrhizi. To ensure the success of the artificial inoculation, the plants were transferred to a humid chamber with a relative humidity of about 95% and 20 to 24° C. for 24 h. The next day the plants were cultivated for 2 days in a greenhouse chamber at 23-27° C. and a relative humidity between 60 and 80%. Then the plants were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture as described below. The plants were allowed to air-dry. Then the trial plants were cultivated for 14 days in a greenhouse chamber at 23-27° C. and a relative humidity between 60 and 80%. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area. The plants which had been treated with an aqueous active compound preparation comprising 300 ppm of the active compounds of examples 8, 9, 11, 15, 16, 17, 18, 19, 20, 22 and 23 showed an infection of 0%, whereas the untreated plants were 60% infected.
| Number | Date | Country | Kind |
|---|---|---|---|
| 09163166.3 | Jun 2009 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP10/58534 | 6/17/2010 | WO | 00 | 12/12/2011 |
