CN100358877C - Process for preparation of fungicidal compositions - Google Patents

Process for preparation of fungicidal compositions Download PDF

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CN100358877C
CN100358877C CNB981191312A CN98119131A CN100358877C CN 100358877 C CN100358877 C CN 100358877C CN B981191312 A CNB981191312 A CN B981191312A CN 98119131 A CN98119131 A CN 98119131A CN 100358877 C CN100358877 C CN 100358877C
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alkyl
group
methyl
halogen
carbon atom
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CN1222301A (en
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B·-W·克卢格
P·格迪斯
L·阿什曼
U·海尼曼
H·盖耶
D·库特
U·菲利浦
T·塞兹
J·施泰特
R·泰曼
H·-W·迪尼
S·杜茨曼
G·汉斯勒
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Bayer AG
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Abstract

New azadioxacycloalkenes have the formula (I), in which A stands for optionally substituted alkane diyl (alkylene); Ar stands for optionally substituted arylene or heteroarylene; E stands for one of the following groupings (a), (b), (c), (d), (e) where Y is oxygen, sulphur, methylene (CH2) or alkylimino (N-R); and Z - G stand for various substituents. Also disclosed are a process for preparing the same and their use as fungicides.

Description

The method for preparing fungicide composition
The application is that application number is 94193669.4, and the applying date is on July 29th, 1994, and denomination of invention is divided an application for the application for a patent for invention of " the azepine dioxane alkene of replacement and as the application of mycocide ".
The present invention relates to new substituted nitrogen heterocyclic dioxane alkene, its preparation method with and as the purposes of mycocide.
5 of some replacement was disclosed already, 6-dihydro-1,4,2-two  piperazines have fungicidal properties (referring to, JP-A 01221371-quotes from the 112:98566t in Chem.Abstracts; JP-A 02001484-quotes from the 113:6381y in Chem.Abstracts).
Yet these compounds are not paid attention to especially.
Have now found that the azepine dioxane alkene of the new replacement of general formula (I)
Figure C9811913100041
Wherein
Optional alkane two bases (alkylidene group) that replace of A representative,
Optional separately arylidene or the inferior heteroaryl that replaces of Ar;
The E representative is with R on 2 1The 1-alkene-1 of base, 1-two bases, or on 2, be with R 22-azepine-1-the alkene-1 of base, 1-two bases, or on 1, be with R 1The 3-oxa-or the 3-thia-1-propylene-2 of base, 3-two bases, or representative is being with the R base and is being with R on 1 on 3 13-azepine-1-the propylene-2 of base, 3-two bases, or representative is with R on 1 21-azepine-1-the propylene-2 of base, 3-two bases, or representative is with R on 1 2The 3-oxa-or the 3-thia-1-azepine-propylene-2 of base, 3-two bases, or representative is being with the R base and is being with R on 1 on 3 21 of base, 3-diaza-1-propylene-2,3-two bases, or optional imino-(" aza-methylene ", the N-R that replaces of representative 3),
Wherein
R represents alkyl,
R 1Represent hydrogen, halogen, cyano group or optional separately alkyl, alkoxyl group, alkylthio, alkylamino or the dialkyl amido that replaces,
R 2Represent hydrogen, amino, cyano group or optional separately alkyl, alkoxyl group, alkylamino or the dialkyl amido that replaces: and
R 3Represent hydrogen, cyano group or optional separately alkyl, alkenyl, alkynyl, cycloalkyl or the cycloalkylalkyl that replaces,
G represents a singly-bound, oxygen or representative optional separately alkane two bases, olefin 2 base, oxa-olefin 2 base, alkynes two bases by halogen, hydroxyl, alkyl, haloalkyl or cycloalkyl substituted, or represents one of following groups:
-Q-CQ-,-CQ-Q-,-CE 2-Q-,-Q-CE 2-,-CQ-Q-CE 2-,-CE 2-Q-CQ-,-Q-CQ-CE 2-,-Q-CQ-Q-CE 2-,-N=N-,-S (O) n-,-CE 2-S (O) n-,-CQ-,-S (O) n-CE 2-,-C (R 4)=N-O-,-C (R 4)=N-O-CE 2-,-N (R 5)-,-CQ-N (R 5)-,-N (R 5)-CQ-,-Q-CQ-N (R 5)-,-N=C (R 4)-Q-CE 2-,-CE 2-O-N=C (R 4)-,-N (R 5)-CQ-Q-,-CQ-N (R 5)-CQ-Q-,-N (R 5)-CQ-Q-CE 2-,-CQ-CE 2-or-N=N-C (R 4)=N-O-,
Wherein
N represents 0,1 or 2 numeral;
Q represents oxygen or sulphur;
R 4Represent optional separately alkyl, alkoxyl group, alkylthio, alkylamino, dialkyl amido or the cycloalkyl that replaces of hydrogen, cyano group or representative and
R 5Represent optional separately alkyl, alkoxyl group or the cycloalkyl that replaces of hydrogen, hydroxyl, cyano group or representative and
Optional separately alkyl, alkenyl, alkynyl, cycloalkyl, aryl or the heterocyclic radical that replaces of Z representative.
Also have found that the azepine dioxane alkene of new replacement that can following acquisition general formula (I):
(a) the first step, when suitable, in the presence of acid acceptor when suitable, in the presence of thinner, make the carboxylic acid derivative of general formula (II) and oxyamine or with its halogenation hydride reaction,
Figure C9811913100061
Wherein
Ar, E, G and Z have above-mentioned connotation and
R represents alkyl;
And the product of the first step is in position, promptly need not intermediate section from, in second step, when suitable, in the presence of acid acceptor and when suitable, in the presence of thinner, react with two replacement alkane of general formula (III),
X-A-X (III)
Wherein
A has above-mentioned connotation, and
X represents halogen, alkylsulfonyloxy or aryl-sulfonyl oxygen, or
(b) in formula (I), G represent oxygen or-CH 2-O-group, and A, Ar, E and
When Z has above-mentioned connotation;
When suitable, in the presence of acid acceptor, and when suitable, in the presence of thinner, the hydroxy aryl compound of general formula (IV) and the compound of logical formula V are reacted,
Wherein
A, Ar and E have above-mentioned connotation;
Z-(CH 2) m-X (V)
Wherein
X and Z have above-mentioned connotation, and
M represents numeral 0 or 1;
And when suitable, subsequently ethyl group is carried out substitution reaction by ordinary method, or
(c) in formula (I), G representative-Q-CH 2-group and A, Ar, E and Z base
When group has above-mentioned connotation,
When suitable in the presence of acid acceptor, and when suitable in the presence of thinner, the halogenated methyl compound of general formula (VI) and the compound of general formula (VII) are reacted,
Figure C9811913100072
Wherein
A, Ar and E have above-mentioned connotation, and
X 1Represent halogen,
Z-Q-H (VII)
Wherein
Q and Z have above-mentioned connotation, or
In the presence of thinner, make the hydroxy alkoxy base acid amides of general formula (VIII) and dewatering agent carry out cyclization when (d) suiting,
Figure C9811913100081
Wherein
A, Ar, E, G and Z have above-mentioned connotation.
Find also that at last the azepine dioxane alkene of the new replacement of general formula (I) has very high Fungicidally active.
When suitable, compound of the present invention can exist with the form of mixtures of various possible isomer, particularly E and Z isomer.Required for protection is any mixture of E and Z isomer and isomer thereof.
Preferred such formula (I) compound of the present invention, wherein
The A representative has alkane two bases of 1 to 3 carbon atom, and its optional alkyl or haloalkyl by halogen or 1 to 4 carbon atom replaces;
Optional separately phenylene or the naphthylidene that replaces of Ar representative, or represent 5 or 6 annular atomses and wherein at least one annular atoms represent oxygen, sulphur or nitrogen, one or two other annular atoms is represented the inferior heteroaryl of nitrogen when suitable, and wherein possible substituting group is preferably selected from:
Halogen, cyano group, nitro, amino, hydroxyl, formyl radical, carboxyl, formamyl, thiocarbamoyl, respectively the do for oneself alkyl of straight or branched, alkoxyl group, alkylthio, alkyl sulphinyl or alkyl sulphonyl, they respectively have 1 to 6 carbon atom, respectively the do for oneself alkenyl of straight or branched, alkenyloxy or alkynyloxy group, they respectively have 2 to 6 carbon atoms, respectively the do for oneself haloalkyl of straight or branched, halogenated alkoxy, halogenated alkylthio, haloalkyl sulfinyl or halogenated alkyl sulfonyl, they respectively have 1 to 6 carbon atom and 1 to 13 identical or different halogen atom, respectively the do for oneself halogenated alkenyl or the halo alkenyloxy of straight or branched, they respectively have 2 to 6 carbon atoms and 1 to 13 identical or different halogen atom, respectively the do for oneself alkylamino of straight or branched, dialkyl amido, alkyl-carbonyl, alkyl carbonyl oxy, carbalkoxy, alkylsulfonyloxy, oxyimino alkyl or Alkoximino alkyl, they each at moieties separately 1 to 6 carbon atom is arranged, or representative respectively the do for oneself alkylidene group or two oxyalkylenes of divalence, they respectively have 1 to 6 carbon atom and are optionally separately replaced or polysubstituted by identical or different straight or branched alkyl that is selected from halogen and/or 1 to 4 carbon atom and/or the substituting group list that contains the straight or branched haloalkyl of 1 to 4 carbon atom and 1 to 9 identical or different halogen atom;
E represents one of following groups:
Figure C9811913100091
Wherein
Y represents oxygen, sulphur, methylene radical (CH 2) or alkyl imino (N-R),
The R representative has the alkyl of 1 to 6 carbon atom,
R 1Represent hydrogen, halogen, cyano group or represent alkyl, alkoxyl group, alkylthio, alkylamino or dialkyl amido, they respectively have 1 to 6 carbon atom and optional separately by halogen, cyano group or C on alkyl 1-C 4Alkoxyl group replaces,
R 2Represent hydrogen, amino, cyano group, or represent alkyl, alkoxyl group, alkylamino or dialkyl amido, 1 to 6 carbon atom is arranged and on their each comfortable moieties separately randomly by halogen, cyano group or C 1-C 4Alkoxyl group replace and
R 3Represent hydrogen, cyano group, or represent alkyl, alkenyl or alkynyl, they have maximum 6 carbon atoms and optional by halogen, cyano group or C 1-C 4Alkoxyl group replaces, or
If representative has 3 to 6 carbon atoms and the cycloalkyl or the cycloalkylalkyl of 1 to 4 carbon atom that suits to have at moieties at cycloalkyl moiety, they are optional separately by halogen, cyano group, carboxyl, C 1-C 4Alkyl or C 1-C 4Carbalkoxy replaces,
G represents singly-bound, oxygen, or represents alkane two bases, olefin 2 base, oxa-alkene two bases, alkynes two bases, and they each have maximum 4 carbon atoms and optional separately by halogen, hydroxyl, C 1-C 4Alkyl, C 1-C 4Haloalkyl or C 3-C 6Cycloalkyl substituted, or represent one of following groups:
-Q-CQ-,-CQ-Q-,-CE 2-Q-,-Q-CE 2-,-CQ-Q-CE 2-,-CE 2-Q-CQ-,-Q-CQ-CE 2-,-Q-CQ-Q-CE 2-,-N=N-,-S (O) n-,-CE 2-S (O) n-,-CQ-,-S (O) n-CE 2-,-C (R 4)=N-O-,-C (R 4)=N-O-CE 2-,-N (R 5)-,-CQ-N (R 5)-,-N (R 5)-CQ-,-Q-CQ-N (R 5)-,-N=C (R 4)-Q-CE 2-,-CE 2-O-N=C (R 4)-,-N (R 5)-CQ-Q-,-CQ-N (R 5)-CQ-Q-,-N (R 5)-CQ-Q-CE 2-,-CQ-CE 2-or-N=N-C (R 4)=N-O-,
Wherein
N represents numeral 0,1 and 2,
Q represents oxygen or sulphur,
R 4Represent hydrogen, cyano group, or represent alkyl, alkoxyl group, alkylthio, alkylamino or dialkyl amido, they respectively have 1 to 6 carbon atom and optional separately by halogen, cyano group or C on alkyl 1-C 4Alkoxyl group replaces, or represents the cycloalkyl that 3 to 6 carbon atoms are arranged, and they are optional by halogen, cyano group, carboxyl, C 1-C 4Alkyl or C 1-C 4Carbalkoxy replace and
R 5Represent hydrogen, hydroxyl, cyano group, or representative is optional by halogen, cyano group or C 1-C 4The alkyl of 1 to 6 carbon atom that alkoxyl group replaces, or representative is optional by halogen, cyano group, carboxyl, C 1-C 4Alkyl or C 1-C 4The cycloalkyl of 3 to 6 carbon atoms that carbalkoxy replaces and
Z represents the alkyl of 1 to 8 carbon atom, and it is optional by halogen, cyano group, hydroxyl, amino, C 1-C 4Alkoxyl group, C 1-C 4Alkylthio, C 1-C 4Alkyl sulphinyl or C 1-C 4Alkyl sulphonyl (can choose wantonly separately by halogen and replace) replaces; or represent alkenyl or alkynyl; they contain maximum 8 carbon atoms and optional separately by the halogen replacement, or represent the cycloalkyl of 3 to 6 carbon atoms, and they are chosen wantonly by halogen, cyano group, carboxyl, phenyl and (choose wantonly by halogen, cyano group, C 1-C 4Alkyl, C 1-C 4Haloalkyl, C 1-C 4Alkoxyl group or C 1-C 4The halogenated alkoxy replacement), C 1-C 4Alkyl or C 1-C 4Carbalkoxy replaces, or represent the heterocyclic radical of optional phenyl, naphthyl or (optional benzene condensed) tool 5 or 6 annular atomses that replace separately, at least one represents oxygen, sulphur or nitrogen in the annular atoms, and if suitable, other has one or two annular atoms to represent nitrogen, and wherein possible substituting group is preferably selected from:
Oxygen (replacing two geminal hydrogen atoms); halogen; cyano group; nitro; amino; hydroxyl; formyl radical; carboxyl; formamyl; thiocarbamoyl; respectively the do for oneself alkyl of straight or branched; alkoxyl group; alkylthio; alkyl sulphinyl or alkyl sulphonyl; they respectively have 1 to 6 carbon atom; respectively the do for oneself alkenyl or the alkenyloxy of straight or branched; they respectively have 2 to 6 carbon atoms; respectively the do for oneself haloalkyl of straight or branched; halogenated alkoxy; halogenated alkylthio; haloalkyl sulfinyl or halogenated alkyl sulfonyl; they respectively have 1 to 6 carbon atom and 1 to 13 identical or different halogen atom; respectively the do for oneself halogenated alkenyl of straight or branched; the halo alkenyloxy; they respectively have 2 to 6 carbon atoms and 1 to 13 identical or different halogen atom; respectively the do for oneself alkylamino of straight or branched; dialkyl amido; alkyl-carbonyl; alkyl carbonyl oxy; carbalkoxy; alkylsulfonyloxy; oximino alkyl or Alkoximino alkyl; they have 1 to 6 carbon atom at moieties separately; the alkylidene group of the divalence of respectively doing for oneself or two oxyalkylenes; they respectively have 1 to 6 carbon atom and are optionally separately replaced or polysubstituted by straight or branched alkyl that is selected from halogen and/or 1 to 4 carbon atom and/or the identical or different substituting group list that contains the straight or branched haloalkyl of 1 to 4 carbon atom and 1 to 9 identical or different halogen atom; or the cycloalkyl of 3 to 6 carbon; heterocyclic radical or heterocyclyl methyl; they respectively have 3 to 7 annular atomses; it is identical or different heteroatoms that 1 to 3 annular atoms is wherein respectively arranged---nitrogen particularly; oxygen and/or sulphur; and phenyl; phenoxy group; benzyl; benzyloxy; styroyl or benzene oxyethyl group, they are optional by being selected from halogen at phenyl moiety; cyano group; nitro; carboxyl; the straight or branched alkyl of formamyl and/or 1 to 4 carbon atom and/or contain the straight or branched haloalkyl of 1 to 4 carbon atom and 1 to 9 identical or different halogen atom and/or contain the straight or branched alkoxyl group of 1 to 4 carbon atom and/or contain the straight or branched halogenated alkoxy of 1 to 4 carbon atom and 1 to 9 identical or different halogen atom and/or the identical or different substituting group list of the alkyl-carbonyl of each self-contained maximum 5 carbon atom or carbalkoxy replaces or polysubstituted.
In definition, saturated or aliphatic unsaturated hydrocarbon as alkyl, alkane two bases, alkenyl or alkynyl, and is connected with heteroatomic situation, as at alkoxyl group, and in alkylthio or the alkylamino, each straight or branched naturally in all cases.
Halogen is represented fluorine, chlorine, bromine or iodine usually, preferred fluorine, chlorine or bromine, particularly fluorine or chlorine.
Specifically, the present invention relates to the compound of formula (I), wherein
A represents methylene radical or dimethylene (second-1,2-two bases), and they can be chosen wantonly by fluorine, chlorine, methyl, ethyl or trifluoromethyl and replace,
The optional separately neighbour who replaces of Ar representative, or to phenylene, or represent furans two bases, thiophene two bases, pyrroles's two bases, pyrazoles two bases, triazole two bases,  azoles two bases, different  azoles two bases, thiazole two bases, isothiazole two bases,  diazole two bases, thiadiazoles two bases, pyridine two bases, pyrimidine two bases, pyridazine two bases, pyrazine two bases, 1,3,4-triazine two bases or 1,2,3-triazine two bases, wherein possible substituting group particularly is selected from:
Fluorine, chlorine, cyano group, methyl, ethyl, trifluoromethyl, methoxyl group, oxyethyl group, methylthio group, methylsulfinyl or methyl sulphonyl,
E represents one of following groups:
Figure C9811913100131
Wherein
Y represents oxygen, sulphur, methylene radical (CH 2) or alkyl imino (N-R),
R represent methylidene, ethyl, just or sec.-propyl, or just, the XOR tertiary butyl,
R 1Represent hydrogen, fluorine, chlorine, bromine, cyano group or represent methylidene, ethyl, propyl group, methoxyl group, oxyethyl group, methylthio group, ethylmercapto group, methylamino-, ethylamino or dimethylamino, they are optional by fluorine, chlorine, cyano group, methoxy or ethoxy replacement;
R 2Represent hydrogen, amino, cyano group, or represent methylidene, ethyl, methoxyl group, oxyethyl group, methylamino-, ethylamino or dimethylamino, they optional separately by fluorine, chlorine, cyano group, methoxy or ethoxy replace and
R 3Represent hydrogen, cyano group, or represent methylidene, ethyl, just or sec.-propyl, just, the XOR tertiary butyl, they are optional separately by fluorine, cyano group, methoxy or ethoxy replacement, or represent allyl group or propargyl, or represent cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropyl methyl, cyclobutylmethyl, cyclopentyl-methyl or cyclohexyl methyl, they optional separately by fluorine, chlorine, cyano group, carboxyl, methyl, ethyl, just or sec.-propyl, methoxycarbonyl or ethoxycarbonyl replace
G represents singly-bound, oxygen or represents methylene radical, dimethylene (second-1,2-two bases), ethene-1,2-two bases, acetylene-1,2-two bases, they optional separately by fluorine, chlorine, hydroxyl, methyl, ethyl, just or sec.-propyl, trifluoromethyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl replace, or represent one of following groups:
-Q-CQ-,-CQ-Q-,-CE 2-Q-,-Q-CE 2-,-CQ-Q-CE 2-,-CE 2-Q-CQ-,-Q-CQ-CE 2-,-Q-CQ-Q-CE 2-,-N=N-,-S (O) n-,-CE 2-S (O) n-,-CQ-,-S (O) n-CE 2-,-C (R 4)=N-O-,-C (R 4)=N-O-CE 2-,-N (R 5)-,-CQ-N (R 5)-,-N (R 5)-CQ-,-Q-CQ-N (R 5)-,-N=C (R 4)-Q-CE 2-,-CE 2-O-N=C (R 4)-,-N (R 5)-CQ-Q-,-CQ-N (R 5)-CQ-Q-or-N (R 5)-CQ-Q-CE 2-,
Wherein
N represents numeral 0,1 or 2,
Q represents oxygen or sulphur,
R 4Represent hydrogen, cyano group or represent methylidene, ethyl, just or sec.-propyl, just, the XOR tertiary butyl, methoxyl group, oxyethyl group, propoxy-, butoxy, methylthio group, ethylmercapto group, rosickyite base, butylthio, methylamino-, ethylamino, third amino, dimethylamino or diethylamino, they are optional separately by fluorine, chlorine, cyano group, methoxy or ethoxy replacement, or represent cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, they optional separately by fluorine, chlorine, cyano group, carboxyl, methyl, ethyl, just or sec.-propyl, methoxycarbonyl or ethoxycarbonyl replace and
R 5Represent hydrogen, hydroxyl, cyano group or represent methylidene, ethyl, just or sec.-propyl, just, different, second month in a season or the tertiary butyl, they are optional separately by fluorine, chlorine, cyano group, methoxy or ethoxy replacement, or represent cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, they optional separately by fluorine, chlorine, cyano group, carboxyl, methyl, ethyl, just or sec.-propyl, methoxycarbonyl or ethoxycarbonyl replace and
The Z represent methylidene, ethyl, just or sec.-propyl, or just, different, secondary, or the tertiary butyl, they are optional separately by fluorine, chlorine, bromine, cyano group, hydroxyl, amino, methoxyl group, oxyethyl group, methylthio group, ethylmercapto group, methylsulfinyl, the ethyl sulfinyl, methyl sulphonyl or ethylsulfonyl (they are optional separately by fluorine and/or chlorine replacement) replace, or representative allyl group, butenyl, 1-methyl-allyl group, propargyl or 1-methyl-propargyl, they are optional separately by fluorine, chlorine or bromine replaces, or representative cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, they are optional separately by fluorine, chlorine, bromine, cyano group, carboxyl, phenyl is (optional by fluorine, chlorine, bromine, cyano group, methyl, ethyl, just or sec.-propyl, just, different, the second month in a season or the tertiary butyl, trifluoromethyl, methoxyl group, oxyethyl group, just or isopropoxy, difluoro-methoxy or trifluoromethoxy replace), methyl, ethyl, just or sec.-propyl, methoxycarbonyl or ethoxycarbonyl replace, or the optional separately substituted phenyl of representative, naphthyl, furyl, tetrahydrofuran base, benzofuryl, THP trtrahydropyranyl, thienyl, benzothienyl, pyrryl, the pyrrolin base, the Pyrrolidine base, the benzopyrrole base, benzo pyrrolin base,  azoles base, the benzoxazol base, different  azoles base, thiazolyl, benzothienyl, isothiazolyl, imidazolyl, benzimidazolyl-, the  di azoly, thiadiazolyl group, pyridyl, pyrimidyl, pyridazinyl, pyrazinyl, 1,2, the 3-triazinyl, 1,2,4-triazinyl or 1,3, the 5-triazinyl, wherein possible substituting group is preferably selected from: oxygen (substituting two geminal hydrogen atoms), fluorine, chlorine, bromine, cyano group, nitro, amino, hydroxyl, formyl radical, carboxyl, formamyl, thiocarbamoyl, methyl, ethyl, just or sec.-propyl, just, different, the second month in a season or the tertiary butyl, methoxyl group, oxyethyl group, just or isopropoxy, methylthio group, ethylmercapto group, just or the iprotiazem base, methylsulfinyl, the ethyl sulfinyl, methyl sulphonyl or ethylsulfonyl, trifluoromethyl, difluoro-methoxy, trifluoromethoxy, the difluoro methylthio group, trifluoromethylthio, trifluoromethyl sulphinyl base or trifluoromethyl sulfonyl, methylamino-, ethylamino, just or isopropylamino, dimethylamino, diethylamino, ethanoyl, propionyl, acetoxyl group, methoxycarbonyl, ethoxycarbonyl, mesyloxy, ethanesulfonyloxy group, the oximino methyl, the oximino ethyl, the methoxyimino methyl, the ethoxy imino methyl, methoxyimino ethyl or ethoxy imino ethyl; Or trimethylene (the third-1; 3-two bases); methylene-dioxy or ethylenedioxy; cyclopropyl; cyclobutyl; cyclopentyl or cyclohexyl; their optional separately fluorine that is selected from; chlorine; methyl; ethyl or just or the identical or different substituting group list of sec.-propyl replace or polysubstituted; and phenyl; phenoxy group; benzyl or benzyloxy, they are respectively at the optional fluorine that is selected from of phenyl moiety; chlorine; bromine; cyano group; nitro; carboxyl; formamyl; methyl; ethyl; just or sec.-propyl; just; different; the second month in a season or the tertiary butyl; trifluoromethyl; methoxyl group; oxyethyl group; just or isopropoxy; difluoro-methoxy; trifluoromethoxy; ethanoyl; the identical or different substituting group list of methoxycarbonyl or ethoxycarbonyl replaces or is polysubstituted.Most preferred one group of The compounds of this invention is such formula (I) compound, wherein
A represents dimethylene (second-1,2-two bases),
Ar represents neighbour-phenylene, pyridine-2, and 3-two bases or thiophene-2,3-two bases,
E represents one of following groups:
Figure C9811913100161
Wherein
R 1And R 2Representation methoxy separately,
G represents oxygen, one of methylene radical or following groups:
-CE 2-O-,-O-CE 2-,-S (O) n-,-CE 2-S (O) n-,-S (O) n-CE 2-,-C (R 4)=N-O-,-O-N=C (R 4)-,-C (R 4)=N-O-CE 2-,-N (R 5)-or-CE 2-O-N=C (R 4)-,
Wherein
N represents numeral 0,1 or 2,
R 4Represent hydrogen, methyl or ethyl and
R 5Represent hydrogen, methyl or ethyl and
The optional separately substituted phenyl of Z representative, pyridyl, pyrimidyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1,2,4-triazinyl or 1,3,5-triazines base, wherein
Possible substituting group is preferably selected from:
Fluorine; chlorine; bromine; cyano group; methyl; ethyl; just or sec.-propyl; just; different; the second month in a season or the tertiary butyl; methoxyl group; oxyethyl group; just or isopropoxy; methylthio group; ethylmercapto group; just or the iprotiazem base; methylsulfinyl; the ethyl sulfinyl; methylsulfonyl or ethylsulfonyl; trifluoromethyl; difluoro-methoxy; trifluoromethoxy; the difluoro methylthio group; trifluoromethylthio; trifluoromethyl sulphinyl base or trifluoromethyl sulfonyl; methoxycarbonyl; ethoxycarbonyl; the methoxyimino ethyl; the ethoxy imino ethyl; methoxyimino ethyl or ethoxy imino ethyl; or methylene-dioxy or ethylenedioxy; they are optional separately by being selected from fluorine; chlorine; the identical or different substituting group list of methyl or ethyl replaces or two replacement; and phenyl; phenoxy group; benzyl or benzyloxy, their each comfortable phenyl moieties are optional by being selected from fluorine; chlorine; bromine; cyano group; methyl; ethyl; just or sec.-propyl; just; different; the second month in a season or the tertiary butyl; trifluoromethyl; methoxyl group; oxyethyl group; just or isopropoxy; the identical or different substituting group list of difluoro-methoxy or trifluoromethoxy replaces or is polysubstituted.
The above-mentioned general group definition or the group definition of preferable range are applicable to the end product of formula (I), and are applicable to and prepare required raw material or intermediate in all cases.
If desired, the definition of these groups can be made up mutually, and in other words, the combination between specified preferred compound scope also is possible.
For example, if make raw material with α-methoxyimino-α-(2-Phenoxyphenyl)-methyl acetate, hydroxylamine hydrochloride and glycol dibromide, the reaction path among the preparation method of the present invention (a) can be summarized with following reaction formula:
Figure C9811913100171
For example, if with 3-[α-methoxyimino-α-(2-hydroxyl-phenyl)-methyl]-5,6-dihydro-1,4,2-two  piperazines and phenmethyl chlorine are made raw material, and the reaction path among the preparation method of the present invention (b) can be with following reaction formula general introduction:
Figure C9811913100181
For example, if with 3-[α-methoxyimino-α-(2-chloromethyl-phenyl)-methyl]-5,6-dihydro-1,4,2-two  piperazines and 2-methylphenol are made raw material, and the reaction path among the preparation method of the present invention (c) can be with following reaction formula general introduction:
Figure C9811913100182
For example, if make raw material with N-(2-hydroxyl-oxyethyl group)-α-methoxyimino-α-(2-phenoxy group-phenyl)-ethanamide, the reaction path among the preparation method of the present invention can be summarized with following reaction formula:
Formula (II) provides the General Definition that needs as the carboxylic acid derivative of the raw material that carries out the inventive method (a).In formula (II), Ar, E, G preferably or particularly have with formula of the present invention (I) compound with Z and describe the relevant preferred or particularly preferred Ar that had mentioned already, E, and G and Z implication: R preferably represent the alkyl of 1 to 4 carbon atom; Particularly methyl or ethyl.
The raw material of formula (II) be known and/or can by known method preparation itself (referring to, EP-A 178826, EP-A 242081, EP-A 382375, EP-A 493711).
Formula (III) provides the general definition of other the two replacement alkane that are used as raw material in the inventive method (a).In the formula (III), A preferably or particularly has the implication of describing the relevant preferred or particularly preferred A that had mentioned already with formula of the present invention (I) compound; X preferably represents chlorine, bromine, mesyloxy, phenylsulfonyloxy or tosyloxy.
The raw material of formula (III) is known organic synthesis compound.
Formula (IV) is provided at the general definition that is used as the hydroxy aryl compound of raw material in the inventive method (a) for preparing general formula (I) compound.In the formula (IV), A, Ar preferably or particularly has the preferred or particularly preferred A that already provided relevant with the description of formula (I) compound, those connotations of Ar and E with E.
The raw material of formula (IV) does not see document so far as yet, and as novel substance, it is the application's a part.
The new hydroxy-aryl compound of formula (IV) can be by following acquisition: when suitable, in the presence of thinner, for example at water, methyl alcohol, ethanol or ethyl acetate exist down, between 0 ℃ to 100 ℃, make the tetrahydropyran oxygen based compound and the acid-respons of general formula (IX), hydrochloric acid for example, sulfuric acid, methylsulfonic acid, Phenylsulfonic acid, tosic acid, or with acid ion exchangers reaction (referring to preparation embodiment).
Figure C9811913100201
Wherein
A, Ar and E have above-mentioned connotation.
The tetrahydropyran oxygen based compound of formula (IX) does not see document so far as yet, and as novel substance, it is the application's a part.
The new tetrahydropyran oxygen based compound of formula (IX) can be by following acquisition: when suitable, in the presence of acid acceptor such as potassium hydroxide, and when suitable, in the presence of thinner such as first alcohol and water, make the reaction of the ester of general formula (X) and oxyamine (if or suitable, with its hydrochloride reaction), and when suitable, at acid acceptor for example in the presence of the salt of wormwood, the intermediate that forms at 0 ℃ of-100 ℃ of chien shih saturated dihalide of original position and above-mentioned general formula (III) again reacts, (referring to, according to the description of the inventive method (a) and preparation embodiment)
Figure C9811913100202
Wherein
Ar, E and R have above-mentioned connotation.
The ester of formula (X) does not see document so far as yet, and as novel substance, it is the application's a part.
The new ester of formula (X) can followingly obtain: with the THP trtrahydropyranyl oxygen base of general formula (XI)-phenylacetic acid ester with ordinary method derivation (referring to preparation embodiment):
Figure C9811913100211
Wherein
Ar and R have above-mentioned connotation.
The THP trtrahydropyranyl oxygen base-phenylacetic acid ester of formula (XI) does not see document so far as yet, and as novel substance, it is the application's a part.
New tetrahydro-pyran oxy-phenylacetic acid the ester of formula (XI) can followingly obtain: when suitable, at catalyzer as in the presence of to the methylene Phenylsulfonic acid, when suitable in the presence of thinner such as tetrahydrofuran (THF), in the hydroxyphenyl acetic acid ester and the dihydropyrane reaction of 0 ℃ to 100 ℃ chien shih general formula (XII)
Figure C9811913100212
Wherein
Ar and R have above-mentioned connotation; (referring to preparation embodiment).
The raw material of formula (XII) is known synthetic compound.
Formula V provides the other general definition that is used as the compound of raw material in the inventive method (b) of preparation general formula (I) compound that is used as.In the formula V, Z preferably or particularly has the implication of describing the relevant preferred or particularly preferred Z that had mentioned already with formula (I) compound; X preferably represents chlorine, bromine, mesyloxy, phenylsulfonyloxy or tosyloxy.
The raw material of formula V is known synthetic compound.
Formula (XI) is provided at the general definition that is used as the halogenated methyl compound of raw material in the inventive method (c) for preparing general formula (I) compound.In the formula (VI), A, Ar and E preferably or particularly have with formula (I) compound describe relevant mentioned already preferably, or particularly preferred A, those connotations of Ar and E; X1 preferably represents fluorine, chlorine, bromine or iodine, particularly chlorine or bromine.
The raw material of formula (VI) does not see document so far as yet, and as novel substance, it is the application's a part.
The new halogenated methyl compound of formula (VI) can followingly obtain: when suitable, at catalyzer as 2,2 '-the azo isobutyronitrile existence is down, if and suit in the presence of thinner such as tetrachloromethane, 0～150 ℃ of methyl compound and for example N-bromine or N-chloro-succinimide reaction (referring to preparation embodiment) of halogenating agent that makes general formula (XIII).
Figure C9811913100221
In the formula
A, Ar and E have above-mentioned connotation.
Need not see document so far as yet as formula (XIII) methyl compound of precursor; As novel substance, it is the application's a part.
The new methyl compound of formula (XIII) can followingly obtain: when suitable, and in the presence of acid acceptor such as potassium hydroxide, and if suitable, in the presence of thinner such as methyl alcohol, make ester and the azanol or the hydroxylamine hydrochloride reaction of formula (XIV),
In the formula
A, E and R have above-mentioned connotation;
And when suitable, in the presence of acid acceptor such as salt of wormwood, make two of product and above-mentioned general formula (III) replace alkane reaction (referring to preparation embodiment) at 0～150 ℃ by the mode that is similar to the inventive method (a).
The precursor of formula (XIV) is known and/or can be by aforementioned known method preparation (referring to EP-A 386561, EP-A 498188, preparation embodiment).
Formula (VII) provides the general definition that is used as the compound of raw material in the inventive method (c) of other preparation general formula (I) compound.In the formula (VII), Q preferably or particularly has with formula (I) compound with Z and describes the relevant above-mentioned preferred or particularly preferred Q that had provided already and those connotations of Z.
The raw material of formula (VII) is known organic synthesis compound.
Formula (VIII) is provided at the general definition that is used as the hydroxy alkoxy base acid amides of raw material in the inventive method (d) for preparing general formula (I) compound.In the formula (VIII), A, Ar, E, G and Z are preferred, or particularly, have with formula (I) compound and describe relevant above-mentioned preferred or particularly preferred A, Ar, E, G and the Z implication that had provided already.
The raw material of formula (XIII) does not see document so far as yet, and as novel substance, it is the application's a part.
The new hydroxy alkoxy base acid amides of formula (VIII) can followingly obtain: make the carboxylic acid derivative of general formula (XV) and the azanol reaction of general formula (XVI):
Figure C9811913100231
Wherein
Ar, E, G and Z have above-mentioned connotation, and
Y represents halogen, hydroxyl or alkoxyl group,
H zN-O-A-OH (XVI)
In the formula
A has above-mentioned connotation;
Reaction conditions is: 0 ℃ to 150 ℃ temperature, when suitable, if in the presence of acid acceptor such as triethylamine, pyridine or 4-dimethylamino-pyridine and suitable, at thinner such as methylene dichloride, toluene or tetrahydrofuran (THF) exist down, (referring to preparing embodiment).
To need formula (XV) carboxylic acid derivative as precursor be known and/or can be by aforementioned known method preparation (referring to EP-A 178826, EP-A 242081, EP-A382375, EP-A 493711).
Need in addition also to be known and/or can to prepare (referring to J.Chem.Soc.Perkin Trans.I 1987,2829-2832) by aforementioned known method as formula (XVI) azanol of precursor.
Method (a) and (b) of the present invention and (c) preferably in the presence of the acid acceptor that is fit to, carry out.The acid acceptor that is fit to is all conventional inorganic or organic basess, comprises, for example, the hydride of basic metal or alkaline-earth metal, oxyhydroxide, amide, alcoholate, acetate, carbonate or supercarbonate, for example, sodium hydride, sodium amide, sodium methylate, sodium ethylate, potassium tert.-butoxide, sodium hydroxide, potassium hydroxide, ammonium hydroxide, sodium acetate, potassium acetate, lime acetate, ammonium acetate, yellow soda ash, salt of wormwood, saleratus, sodium bicarbonate or volatile salt, and also comprise tertiary amine, as Trimethylamine 99, triethylamine, Tributylamine, N, accelerine, N, N-dimethyl-benzylamine, pyridine, the N-methyl piperidine, N, N-dimethyl aminopyridine, diazabicyclooctane (DABCO), Diazabicyclononene (DBN) or diazabicylo hendecene (DBU).
Enforcement the inventive method (a) and (b) and the thinner that is fit to (c) are water and organic solvent.Comprise, particularly, the optional halogenated hydro carbons of aliphatic, alicyclic or aromatics, as, gasoline, benzene, toluene, dimethylbenzene, chlorobenzene, dichlorobenzene, sherwood oil, hexane, hexanaphthene, methylene dichloride, chloroform, tetracol phenixin; Ethers, as ether, diisopropyl ether, two  alkane, tetrahydrofuran (THF) or glycol dimethyl ether or ethylene glycol diethyl ether; Ketone, as acetone, butanone or mibk; Nitrile, as acetonitrile, propionitrile or phenyl cyanide; Amides, as N, dinethylformamide, N,N-dimethylacetamide, N-methyl-formanilide, N-Methyl pyrrolidone or HMPA; The ester class is as methyl acetate or ethyl acetate; The sulfoxide class is as dimethyl sulfoxide (DMSO); Alcohols, as methyl alcohol, ethanol, just or Virahol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether; The mixture of they and water, or pure water.
Method of the present invention (d) is preferably carried out in the presence of dewatering agent.The dewatering agent that is fit to is conventional anhydro compounds, particularly acid anhydrides, as, phosphorus oxide (V) (Vanadium Pentoxide in FLAKES).
The suitable thinner of implementing the inventive method (d) is conventional inert organic solvents.Comprise, particularly aliphatic, the optional halogenated hydro carbons of alicyclic or aromatics, for example, gasoline, benzene, toluene, dimethylbenzene, chlorobenzene, dichlorobenzene, sherwood oil, hexane, hexanaphthene, methylene dichloride, chloroform, tetracol phenixin; Ethers, as ether, diisopropyl ether, two  alkane, tetrahydrofuran (THF) or glycol dimethyl ether or ethylene glycol diethyl ether; Ketone, as acetone, butanone or methyl iso-butyl ketone (MIBK); Nitrile, as acetonitrile, propionitrile or benzonitrile; Amides, as N, dinethylformamide, N,N-dimethylacetamide, N-methyl-formanilide, N-Methyl pyrrolidone or HMPA; The ester class is as methyl acetate or ethyl acetate; The sulfoxide class is as dimethyl sulfoxide (DMSO).
Implement method (a) and (b) of the present invention, (c) and (d) time, temperature of reaction can change in wide range.Usually, these methods can be carried out between-20 ℃ to+200 ℃, preferably the temperature between 0 ℃ and 150 ℃.
When implementing the inventive method (a), every mole formula (II) carboxylic acid derivative adopts 1 to 5 mole usually, preferred 1.0 to 2.5 moles azanol or hydroxylamine hydrochloride and common 1 to 10 mole, and preferred 1.0 to 5.0ml formula (III) two replaces alkane.
When implementing the inventive method (b), every mole formula (IV) hydroxy aryl compound adopts 0.5 to 2.0 mole usually, preferred 0.9 to 1.2 mole formula V compound.
When implementing the inventive method (c), every mole formula (VI) halogenated compound adopts 1 to 5 mole usually, preferred 1.5 to 3 moles formula (VII) compound.
When implementing the inventive method (d), every mole formula (VIII) hydroxy alkoxy base acid amides adopts 1 to 5 mole usually, preferred 1.5 to 4 moles dewatering agent.
In all cases, by known method react, processing and reaction product isolated (referring to preparation embodiment).
Active compound of the present invention has strong microbiocidal activity and can actually be used for preventing and treating harmful microorganism.Active compound is suitable as plant protection product, particularly as mycocide.
Mycocide in the plant protection is applicable to control Plasmodiophoromycetes (Plasmodiophoromycetes); oomycetes subclass (Domycetes); Chytridiomycetes (Chytridiomycetes); Zygomycetes (Zygomycetes); Ascomycetes (Ascomycetes), Basidiomycetes (Basidiomycetes) and imperfect fungi (Deuteromycetes).
Having that the pathogenic organisms body of above-mentioned some fungal disease of listing can be mentioned is for example following, but never is limited to this:
Pythium is as sweet potato white rot germ;
Phytophthora is as the potato phytophthora;
False Peronospora is as Pseudoperonospora humuli or downy mildew of cucurbits bacterium;
Plasmopara is as the downy mildew of garpe bacterium;
Peronospora is as Peronospora pisi or rape frost bacterium;
Erysiphe is as the powdery mildew of cereals bacterium;
Sphaerotheca is as powdery mildew of cucumber spherical shell bacterium;
Podosphaera is as the apple mildew bacterium;
Venturia is as apple black star bacteria;
Caryosphere shell Pseudomonas, as barley reticulate pattern germ or stripe disease of barley (conidial form:
Drechslera, sexual propagation: Helminthosporium);
Cochliobolus belongs to, as standing grain cochliobolus (conidial form: Drechslera, sexual propagation: Helminthosporium);
The monospore rust belongs to, as Kidney bean monospore rest fungus;
The handle rust belongs to, as the wheat leaf rust bacterium;
Tilletia is as wheat net bunt bacterium;
Ustilago is as naked bloom bacterium or black loose smut of oat bacterium;
The film lead fungi belongs to, as Rhizoctonia solani Kuhn;
Magnaporthe grisea belongs to, as piricularia oryzae;
Fusarium is as yellow Fusarium;
Staphlosporonites is as grayish green botrytis;
Septoria is as wheat class grain husk spot blight septoria musiva bacterium;
Leptosphaeria is as Leptosphaeria nodorum;
Cercospora is as Cercospora canescens;
Alternaria belongs to, as the black spot of cabbage Alternariaspp and
False little cercospora is as Pseudocercosporella herpotrichoides.
Plant makes its over-ground part that can handle plant, vegetative propagation rhizome and seed and soil to the good drug-resistant of this active compound of the desired concn of controlling plant diseases.
In this article, active compound of the present invention can be used for successfully preventing and treating the disease of fruit tree and crop especially, for example prevents and treats the phytophthora germ, or control wheat class disease, as caryosphere shell Pseudomonas germ.
In addition, active compound of the present invention has the activity of the good following disease of control: for example powdery mildew of cereals bacterium, standing grain cochliobolus, ball cavity bacteria (Leptosphaeria nodorum), Fusarium germ on false little tail spore bacterium (Pseudocercosporella herpotrichoides) and the cereal class, prevent and treat piricularia oryzae and Rhizoctonia solani Kuhn, and have the external activity of wide spectrum.
According to its concrete physics and/or chemical property, active compound can change into regular dosage form, as solution, and emulsion, suspension agent, pulvis, foaming agent, paste, granule, aerosol is used for polymkeric substance and the trickle capsule of application composition and the ULV cold-peace thermal fog of seed.
These type agent can be produced in known manner, for example, active compound and weighting agent (being liquid solvent, the liquefied gas under the pressure) are mixed, and/or mix, and the optional tensio-active agent (being emulsifying agent and/or dispersion agent and/or pore forming material) that uses with solid carrier.Use water as under the situation of weighting agent, organic solvent also can be used as solubility promoter.As liquid solvent, suitable mainly contains: aromatic substance, and as dimethylbenzene, toluene or alkylnaphthalene, chloro aromatic substance or chlorinated aliphatic hydrocarbon, as the chlorinated benzene class, polyvinyl chloride-base or methylene dichloride, aliphatic hydrocrbon, as hexanaphthene or paraffin, mineral oil fraction for example, alcohols, as butanols or ethylene glycol with and ether and ester, ketone, as acetone, methylethylketone, methyl isopropyl Ketone or pimelinketone, intensive polar solvent, as dimethyl formamide or dimethyl sulfoxide (DMSO), and water; Liquefied gas weighting agent or carrier are meant under envrionment temperature and the barometric point it is the liquid of gas, aerosol propellant for example, and as halohydrocarbon and butane, propane, nitrogen and carbonic acid gas; What solid carrier was fit to has: clay, and talcum, chalk, quartz, attapulgite, montmorillonite or diatomite and the synthetic mineral matter that grinds, as high dispersive silicon-dioxide, alumina and silicate; Be used for suitable the having of solid carrier of granule: for example crushing and broken natural mineral matter such as calcite, marble, float stone, sepiolite and rhombspar, and the synthetic particle of organic and inorganic powder and following organic particle: wood sawdust, coconut husk, corn cob and tobacco stem; What emulsifying agent and/or pore forming material were fit to has: for example nonionic and anionic emulsifier, and as polyoxyethylene fatty acid ester, polyoxyethylene aliphatic alcohol ether, for example, alkaryl polyglycol ether, alkylsulfonate, alkyl-sulphate, arylsulphonate and albumin hydrolysate; What dispersion agent was fit to has: for example, and lignin sulfite waste liquor and methylcellulose gum.
Can use the carboxymethyl cellulose and the natural and synthetic polymer of tackiness agent such as powdery, particle or latex form in the preparation, as gum arabic, polyvinyl alcohol and polyvinyl acetate, and natural phospholipid, as kephalin and Yelkin TTS, and synthetic phospholipid.Other tackiness agent can be mineral oil and vegetables oil.
Also may use dyestuff, as mineral dye, ferric oxide for example, titanium oxide and Prussian blue, and organic dye, as alizarine dyestuff, azoic dyestuff and metal phthalocyanine dyestuff and micro-nutrients such as iron, manganese, boron, copper, cobalt, molybdenum and zinc salt.
Usually the active compound that contains weight ratio 0.1 to 95% in the preparation, preferred 0.5 to 90%.
Active compound of the present invention can itself or with its dosage form, use with the form of the mixture of known mycocide, bactericide, miticide, nematocides or sterilant, enlarging action spectrum, or for preventing the progressively foundation of resistance.In many cases, can obtain synergism, in other words, the activity of mixture exceeds the activity of single component.
Particularly advantageous component is a following compounds for example in the mixture:
Mycocide:
The 2-aminobutane, 2-phenylamino-4-methyl-6-cyclopropyl-pyrimidine; 2 ', 6 '-two bromo-2-methyl-4 '-trifluoromethoxy-4 '-Trifluoromethyl-1,3-thiazole-5-formylaniline; 2,6-two chloro-N-(4-trifluoromethyl phenmethyl) benzamide; (E)-2-methoxyimino-N-methyl-2-(2-phenoxy phenyl) ethanamide oxine vitriol; (E)-and and 2-{2-[6-(2-cyano group-phenoxy group) pyrimidine-4-oxygen base] phenyl }-the 3-methoxy-methyl acrylate; (E)-and methoxyimino [α-(oxy-o-cresyl)-o-tolyl] methyl acetate; 2-phenylphenol (OPP), Aldimorph, Ampropylfos, anilazine; Penta ring azoles, the spirit of withering of M 9834, iodine, benomyl; Binapacryl, biphenyl, Bitertanol, blasticidin-S; Bromuconazole, bupirimate, fourth Saite, lime sulfur; Difoltan, captan, carbendazim, carboxin; Chinomethionate, chloroneb, chloropicrin, Bravo; Chlozolinate, cufraneb, white urea cyanogen, cyproconazole; Cyprofuram, mildew-resistant phenol, diclobutrazol, Euparen; Diclomezine, botran, the mould prestige of second, Difenoconazole; The phonetic alcohol of first, dimethomorph, alkene azoles alcohol, clear mite is general; Diphenylamines, dipyrithion, Plondrel, Delan; Dodine, drazoxolon, the gram bacterium looses epoxy azoles (epoxyconazole); Pyrimethamine, kobam, two chlorobenzene pyrimidines, benzene cyanogen azoles; The spirit of withering of one first furan is planted the clothing ester, fenpiclonil, fenpropidin; Butadiene morpholine, triphenyltin acetate, triphen hydroxyl tin, fervam; Ferimzone, fluazinam, Fludioxonil; Fluoromide, fluquinconazole, fluorine azoles; Flusulfamide, flutolanil, Flutriafol; Folpet, aliette, Rabcide; Furidazol, furalaxyl, seed dressing amine; The biguanides suffering, hexachloro-benzene, own azoles alcohol; The different  azoles of first hydroxyl, imazalil, acid amides azoles; Biguanide spicy acid salt, IBP, iprodione; Isoprothiolane, kasugarnycin, copper agent such as Kocide SD; Copper naphthenate, basic copper chloride, copper sulphate; Cupric oxide, quinolinone and Bordeaux mixture, two for mixture; Mancozeb, maneb, mepanipyrim; Mebenil, metalaxyl, mefconazole; Methasulfocarb, load bacterium amine, Carbatene; Metsulfovax, nitrile bacterium azoles, Sankel; Nitrothal-isopropyl, nuarimol, fenfuram; Dislike acid amides, oxamocarb, oxycarboxin; Perfurazoat, penconazole, Pencycuron; Pimaricin, piperidines is peaceful, Polyoxin; Allyl isothiazole, prochloraz, SP 751011; Propamocarb, propiconazole, propineb; Ppyrazophos, pyrifenox, pyrimethanil; Pyroquilon, pentachloronitrobenzene, sulphur and sulphur preparation; Tebuconazole, phthalein cumfrey, tecnazene; Fluorine ether azoles, probenazole, thicyofen; Thiophanate methyl, thiram, methyl stands withered spirit; Tolyfluanid, triazolone, Triadimenol; Azoles bacterium piperazine, poplar bacterium amine, tricyclazole; Cyclomorpholine, fluorine bacterium azoles, triforine; Triticonazole, zineb, ziram.
Bactericide:
Mix gossypol, mildew-resistant phenol, N-Serve, Sankel, kasugamycin, octhilinone, furancarboxylic acid, terramycin, allyl isothiazole, Streptomycin sulphate, phthalein cumfrey, copper sulfate and other copper agent.
Insecticide/miticide/nematocides:
Avermectin, acephate, fluorine ester chrysanthemum ester, alanycarb, aldicarb, nail body Cypermethrin, amitraz, avermectin (avermectin), AZ60541, azadirachtin, triazotion, R-1582, azocyclotin, bacillus thuringiesis, 4-bromo-2-(4-chloro-phenyl-)-1-(ethoxymethyl)-5-(trifluoromethyl)-1H-pyrazoles-3-formonitrile HCN, benzene  prestige, benfuracarb, desinsection mite, second body cyfloxylate, bifenthrin, Osbac, bromo-ether chrysanthemum ester (brofenprox), bromofos mixes penta prestige, Buprofezin, butocarboxim, butyl pyridaben, cadusafos, SevinCarbaryl, carbofuran, carbophenothion, carbosulfan, Padan, cloethocarb, chlorethoxyfos, Zaprawa enolofos, UC 62644, chlormephos, N-[(6-chloro-3-pyridyl)-methyl]-N '-cyano group-N-methyl-second imino-acid amides, Chlorpyrifos 94, chlorpyrifos_methyl, cis resmethrin, lambda-cyhalothrin, four mite piperazines, cynock, cycloprothrin, cyfloxylate, cyhalothrin, cyhexatin, Cypermethrin, fly eradication amine, Deltamethrin, demeton_S_methyl, different one zero five nine II, different suction phosphorus II, methamidophos, diazinon, chloro line phosphorus, SD-1750, dicliphos, Carbicron, Nialate, diflubenzuron, Rogor, dimethylvinphos, two  sulphur phosphorus, thiodemeton, Hinosan, emamectin, esfenvalerate removes the aphid prestige, Nialate, ether chrysanthemum ester, ethoprop, ether chrysanthemum ester, etrimfos, Nemacur, fenazaquin, mite is finished tin, fenitrothion 95, fenobucarb, fenothiocarb, ABG-6215, Fenvalerate, fenpyrad, azoles mite ester, Tiguvon, fenvalerate, fipronil, fluazinam, fluazuron, flucycloxuron, flucythrinate, flufenoxuron, fluorine ether chrysanthemum ester (flufenprox), taufluvalinate, N-2790, peace fruit, colophonate, fubfenprox, furathiocarb, phenyl-hexachloride, heptenophos, fluorine bell urea, hexythiazox, imidacloprid, iprobenfos, isazofos, isofenphos, isoprocarb,  azoles phosphorus, ivermectin is gone into-lambda-cyhalothrin lufenuron, the Malathion, menazon, Phosdrin, the Tiguvon sulfoxide, Halizan, methacrifos, acephatemet, first thiophene sulphur phosphorus, methiocarb, methomyl, metolcarb, Mil's times rhzomorph, monocrotophos, moxidectin, naled, NC184, nitenpyram, omethoate, grass oxime prestige, sulfone is inhaled sulphur phosphorus, oxydeprofos, the Malathion, methyl Malathion, permethrin, Tsidial, phorate, Phosalone, R-1504, phosphamidon, Volaton, Aphox, methylpyrimidine sulphur phosphorus, pirimiphos-ethyl, Profenofos, Fac, pymefrozin, pyrachlophos, pyraclofos, pyridaphenthione, pyresmethrin, pyrethrum, pyridaben, pyrimidifen, pyriproxyfen, Resitox, salithion, cadusafos, silafluofen, sulfotep, first Toyodan, tebufenozide, tebufenpyrad, special fourth pirimiphos-ethyl, Teflubenzuron, tefluthrin, temephos, terbam, special fourth phorate, tetrachlorvinphos, thiafenox, UC-51762, hexanone oxime prestige, thiometon, quinoline line phosphorus, thuricin, tralomethrin, triarathen, triazophos, triazuron, Trichlorphon, desinsection is grand, trimethacarb, the intact sulphur phosphorus that goes out, Cosban, dimethylbenzene prestige, YI 5301/5302, zetamethrin.
Also can with other known activity compound such as weedicide or with the mixing of chemical fertilizer and growth regulator.
Active compound can use with the type of service of its preparation or its preparation, and described preparation type of service is as can directly using solution, suspension agent, " Spritz " (wetting properties) pulvis, paste, soluble powder, pulvis and granule.They use with ordinary method, for example pour, and spraying, atomizing spreads fertilizer over the fields, and dusts, and bubbles brushing or the like.Available in addition ultra-low volume method is used compound, or active agent preparations or active compound itself are injected soil.Also can handle the seed of plant.
When handling plant part, the activity compound concentration in the type of service can change on a large scale:
Usually, between weight ratio 1 and 0.0001%, preferably in weight ratio 0.5 and 0.001% use.
Handle kind of a period of the day from 11 p.m. to 1 a.m, per kilogram seed demand 0.001 is to 50g usually, the active compound of preferred 0.01 to 10g amount.
When handling soil, needing the concentration of active compound at point of application is weight ratio 0.00001 to 0.1%, preferred weight ratio 0.0001 to 0.02%.
Preparation embodiment
Embodiment 1
Under 20 ℃, 1.8g (25mmol) hydroxylammonium salt acidulants is imported in the 20ml methyl alcohol, and slowly add the 20ml methanol solution of 3.3g potassium hydroxide (86%).Add 4.0g (12.8mmol) α-methoxyimino-α-[2-(2-methyl-phenoxy group-methyl)-phenyl]-methyl acetate subsequently in batches, then reaction mixture is stirred down at 40 ℃, finish (thin-layer chromatography) until reaction.At first, then 10.8g (59mmol) glycol dibromide is added this reaction mixture with 1.7g (12.8mmol) salt of wormwood.This mixture was stirred 12 hours down at 65 ℃, be cooled to 20 ℃ subsequently, and filter.Filtrate concentrates under pump vacuum, and with residue through silica gel chromatography (toluene/acetone, 9: 1 volume ratios).
Obtain 1.4g (theoretical value 33%) 3-{ α-methoxyimino-α-[2-(2-methyl-phenoxy group-methyl)-phenyl]-methyl }-5,6-dihydro-1,4,2-two  piperazines.
Refractive index: n D 20=1.5705.
Can similar embodiment 1 and list in down according to other example of formula (I) compound of preparation method's of the present invention general description preparation and to tabulate in 1.
With being marked on CDCl in the tetramethylsilane work 3Middle record 1The H-NMR spectrum, the data that provide are normally made the δ value with chemical shift.shifts?as?δ?values
Table 1:The embodiment of formula (I) compound
Figure C9811913100352
Figure C9811913100361
Figure C9811913100371
Figure C9811913100381
Figure C9811913100391
Figure C9811913100401
Figure C9811913100411
Figure C9811913100431
Figure C9811913100441
Figure C9811913100451
Figure C9811913100461
Figure C9811913100471
Figure C9811913100481
Figure C9811913100491
Figure C9811913100501
Figure C9811913100511
Figure C9811913100521
Figure C9811913100531
Figure C9811913100541
Figure C9811913100561
Figure C9811913100571
Figure C9811913100581
Figure C9811913100591
Figure C9811913100611
Figure C9811913100621
Figure C9811913100641
Figure C9811913100651
Figure C9811913100671
Figure C9811913100681
Figure C9811913100691
Figure C9811913100721
Figure C9811913100731
Figure C9811913100751
Figure C9811913100761
Figure C9811913100771
Figure C9811913100781
Figure C9811913100791
Figure C9811913100801
Figure C9811913100811
Figure C9811913100821
Figure C9811913100831
Figure C9811913100841
Figure C9811913100851
Figure C9811913100861
Figure C9811913100871
Figure C9811913100881
Figure C9811913100891
Figure C9811913100901
Figure C9811913100911
Figure C9811913100921
Figure C9811913100941
Figure C9811913100951
Figure C9811913100961
The compound that provides with embodiment 60 in the table 1 can for example be prepared as follows:
The oil white oil suspension of 60% concentration of 0.3g (6mmol) sodium hydride is added to 1.5g (6mmol) 3-[α-methoxyimino-α-(2-hydroxyl-phenyl) methyl under ice bath]-5,6-dihydro-1,4,2-two  piperazines, 0.9g (6mmol) 4,6-two chloro-pyrimidines and 30ml N are in the mixture of dinethylformamide.After removing ice bath, reaction mixture was stirred 15 hours at 20 ℃.Concentrate under the oil pump vacuum then, residue is handled with ethyl acetate, washes with water, uses dried over sodium sulfate, and filters.Pump vacuum is distillation down, carefully solvent is removed from filtrate.
Obtain 1.9g (theoretical value 86%) 3-{ α-methoxyimino-α-[2-(6-chloro-pyrimidine-4-oxygen base)-phenyl]-methyl }-5,6-dihydro-1,4,2-two  piperazines are the oily resistates.
The compound that provides with embodiment 61 in the table 1 can for example be prepared as follows:
With 0.3g (0.9mmol) 3-{ α-methoxyimino-α-[2-(6-chloro-pyrimidine-4-oxygen base)-phenyl]-methyl }-5,6-dihydro-1,4,2-two  piperazines, 0.1g (0.9mmol) 2-hydroxy benzonitrile, 0.1g (0.9mmol) salt of wormwood, one little spoonful of cupric chloride (I) and 5ml N, the mixture of N-dimethyl-methane amide stirred 15 hours at 100 ℃, concentrated under the oil pump vacuum then, residue is handled with ethyl acetate, wash with water, use dried over sodium sulfate, and filter.Filtrate is concentrated residue silica gel chromatography (adopting hexane/acetone, 7: 3 volume ratios).
Obtain 0.3g (theoretical value 81%) 3-{ α-methoxyimino-α-[2-(6-(2-cyano group-phenoxy group)-pyrimidine-4-oxygen base)-phenyl]-methyl }-5,6-dihydro-1,4,2-two  piperazines, 82 ℃ of fusing points.
The compound that provides with embodiment 58 in the table 1 can for example be prepared as follows:
Figure C9811913100991
With 0.5g (2mmol) 3-[α-methoxyimino-α-(2-hydroxyl-phenyl)-methyl]-5,6-dihydro-1,4, the mixture of 2-two  piperazines, 0.3g (2.2mmol) 2-methyl-benzyl chloride, 0.4g (2.5mmol) salt of wormwood and 10ml acetonitrile refluxed 15 hours, concentrate then, residue is handled with methylene dichloride, washes with water, use dried over sodium sulfate, and filter.Under pump vacuum, distill, carefully solvent is removed from filtrate.
Obtain 0.4g (theoretical value 59%) 3-{ α-methoxyimino-α-[2-(2-methyl-benzyloxy)-phenyl]-methyl }-5,6-dihydro-1,4,2-two  piperazines, 142 ℃ of fusing points.
In addition, the compound according to embodiment 1 can obtain can for example be prepared as follows:
Figure C9811913100992
With 0.75g (2.4mmol) 3-[α-methoxyimino-α-(2-brooethyl-phenyl)-methyl]-5,6-dihydro-1,4,2-two  piperazines and 0.70g (6.4mmol) 2-methyl-phenol are dissolved in the 15ml dimethyl formamide, and after this mixture is cooled to-10 ℃, slowly add 0.21g (7.0mmol) sodium hydride (80% concentration).After removing cryostat, reaction mixture was stirred 14 hours not being higher than under 25 ℃ the temperature, pour into subsequently in the long-pending water of general diploid.After rocking with ethyl acetate, isolate organic phase,, use dried over sodium sulfate with the washing of 2N sodium hydroxide solution, and filtration.Under reduced pressure distillation is carefully removed solution from filtrate.
Obtain 0.40g (theoretical value 49%) 3-{ α-methoxyimino-α-[2-(2-methyl-phenoxy group-methyl)-phenyl]-methyl }-5,6-dihydro-1,4,2-two  piperazine (refractive indexs: n D 20=1.5705).
The compound that provides with embodiment 19 in the table 1 can for example be prepared as follows:
Figure C9811913101001
0.20g (0.56mmol) N-(2-hydroxyl-oxyethyl group)-α-methoxyimino-α-[2-(2,4-dimethyl-phenoxy group-methyl)-phenyl]-ethanamide is dissolved in the 3ml chloroform, and adds 0.25g (1.76mmol) phosphorus oxide (V) down at 0 ℃.This reaction mixture was stirred 1 hour at 20 ℃, reflux then and stirred 4 hours down, pour into subsequently in the long-pending water of general diploid, and rock.After organic phase was isolated, water extracted three times with chloroform again.Merge organic extract liquid, use dried over mgso, concentrated then, and with column chromatography purifying (silica gel; Toluene/acetone, 10: 1).
Obtain 84mg (theoretical value 42%) 3-{ α-methoxyimino-α-[2-(2,4-dimethyl-phenoxy group-methyl)-phenyl]-methyl }-5,6-dihydro-1,4,2-two  piperazines.
1H?NMR(D 6-DMSO，δ)：4.87，3.84，4.38，4.10ppm。
The raw material of formula (IV)
Embodiment (IV-1)
Figure C9811913101011
With 9.0g (28mmol) 3-[α-methoxyimino-α-(2-tetrahydropyrans-2-oxygen base)-benzyl]-5,6-dihydro-1,4, the 90ml methanol solution of-two  piperazines and 1.8g ion-exchanger " Lewatit SPC 108 " stirred 15 hours down at 20 ℃, then this mixture is concentrated under pump vacuum, residue is handled with methylene dichloride, and filters.Filtrate concentrates under pump vacuum, residue silica gel chromatography (adopting hexane/acetone, 7: 3 volume ratios).
First fraction that obtains is 0.6g (theoretical value 9%) Z-{3-[α-methoxyimino-α-(2-hydroxyl-phenyl)-methyl]-5,6-dihydro-1,4,2-two  piperazines }, be amorphous products; Second fraction is 3.3g (theoretical value 50%) E-{3-[α-methoxyimino-α-(2-hydroxyl-phenyl)-methyl]-5,6-dihydro-1,4,2-two  piperazines }, 153 ℃ of fusing points.
The raw material of formula (IX)
Embodiment (IX-1)
Figure C9811913101021
The potassium hydroxide aqueous solution and 17g (58mmol) α-methoxyimino-α-(2-tetrahydropyrans-2-oxygen base-phenyl)-methyl acetate of 13.9g (211mmol) 85% concentration are added in the 290ml methanol solution of 6.8g (98mmol) hydroxylammonium salt acidulants, and this mixture was stirred one hour down at 40 ℃.Add 7.7g (56mmol) salt of wormwood, and be added dropwise to 42.5g (226mmol) glycol dibromide.Then mixture was refluxed 15 hours, under pump vacuum, concentrate subsequently.Residue is handled with methylene dichloride, washes with water, uses dried over sodium sulfate, and filters.Filtrate is concentrated, and with residue through silica gel chromatography (adopting hexane/acetone, 7: 3 volume ratios).
Obtain 9.0g (theoretical value 49%) 3-[α-methoxyimino-α-(2-tetrahydropyrans-2-oxygen base)-benzyl]-5,6-dihydro-1,4,2-two  piperazines are the oily product.
The raw material of formula (X)
Embodiment (X-1)
Figure C9811913101031
202g (1.81mol) potassium tert.-butoxide is imported in 2 liters of trimethyl carbinols, and to the 500ml t-butanol solution that wherein adds 564g (4.93mol) uncle's butyronitrile and 411g (1.64mol) 2-tetrahydro-pyran oxy-phenylacetic acid methyl esters.After 90 minutes, 350g (2.47mol) methyl-iodide is added dropwise to, and mixture was stirred 15 hours at 20 ℃.Under pump vacuum, concentrate then, and residue is handled with methyl tertiary butyl ether, use dried over sodium sulfate, and filter.Residue produces crystallization with ether digestion, and this product is emanated through suction filtration.
Obtain 69.3g (theoretical value 15%) α-methoxyimino-α-(2-tetrahydropyrans)-2-oxygen base-phenyl)-methyl acetate, 79 ℃ of fusing points.
The raw material of formula (XI)
Embodiment (XI-1)
Figure C9811913101032
With 500g (3.0mol) 2-hydroxyl-phenyl-acetic acid methyl esters 506g (6.0mol) 3, the 4-dihydropyrane, one little spoonful of tosic acid and 2.5 liters of tetrahydrofuran (THF)s stirred 15 hours at 20 ℃, stirred with 10% ice-cold concentration potassium hydroxide aqueous solution then, add sodium sulfate, and mixture is filtered.Under pump vacuum, distill, carefully solvent is removed from filtrate.
Obtain 698g (theoretical value 99%) 2-tetrahydro-pyran oxy-phenyl-acetic acid methyl esters, be the oily residue.
The raw material of formula (VI)
Embodiment (VI-1)
Figure C9811913101041
With 0.50g (2.13mmol) 3-[α-methoxyimino-α-(2-methyl-phenyl)-methyl]-5,6-dihydro-1,4,2-two  piperazines and 0.57g (3.2mmol) N-bromo-succinimide import the 10ml tetracol phenixin, and add after the 200mg azo isobutyronitrile, mixture was refluxed 4 hours.After adding 0.57g (3.2mmol) N-bromo-succinimide again, mixture was refluxed one hour again.With postcooling and filtration, filtrate is concentrated, and residue is carried out chromatogram (silica gel; Toluene/acetone, 10: 1) handle.
Obtain 20mg (theoretical value 30%) 3-[α-methoxyimino-α-(2-bromo-methyl-phenyl)-methyl]-5,6-dihydro-1,4,2-two  piperazines.
1H?NMR(CDCl 3，δ)：4.4ppm。
The raw material of formula (XIII)
Embodiment (XIII-1)
Figure C9811913101051
19.6g (0.283mol) hydroxylammonium salt acidulants is imported 150ml methyl alcohol, and slowly add the 150ml methanol solution of 36.9g (0.565mol) potassium hydroxide (86% concentration).Add 30g (0.145mol) α-methoxyimino-α-(2-methyl-phenyl)-methyl acetate then in batches.Under 50 ℃, mixture was stirred 3 hours.Add 20g (0.145mol) salt of wormwood and 122g (0.65mol) glycol dibromide at 20 ℃ subsequently, and this mixture was stirred 17 hours down at 65 ℃.After the mixture cooling, filter with suction, filtrate is concentrated, and residue is carried out chromatogram (silica gel; Toluene/acetone, 15: 1) handle.
Obtain 15.2g (theoretical value 45%) 3-[α-methoxyimino-α-(2-methyl-phenyl)-methyl]-5,6-dihydro-1,4,2-two  piperazines.
1H?NMR(CDCl 3，δ)：2.2ppm。
The raw material of formula (XIV)
Embodiment (XIV-1)
Figure C9811913101052
187.5g (1.673mol) potassium tert.-butoxide is dissolved in the 1875ml trimethyl carbinol.The 500ml t-butanol solution of 471.5g (4.57mol) nitrite tert-butyl and 250g (1.525mol) 2-methyl-phenyl-acetic acid methyl esters is metered into, medium temperature is not risen to be higher than 50 ℃.Mixture was stirred 90 minutes, rise to 30 ℃ from 20 ℃.Be added dropwise to 326.5g (2.3mol) methyl-iodide then, and reaction mixture was stirred 14 hours at 20 ℃.Solution is removed in distillation under pump vacuum subsequently, and residue is handled with 2 premium on currency, and with mixture ethyl acetate extraction three times.Merge organic phase, use dried over sodium sulfate, and filter.Filtrate is concentrated, and residue is handled with the 250ml Virahol, and adds entry under refluxing, until the mixture feculence.
With mixture be cooled to 0 ℃ and stirred 60 minutes after, with the crystalline product isolated by filtration under suction that obtains.
Obtain 84.5g (theoretical value 27%) α-methoxyimino-α-(2-methyl-phenyl)-methyl acetate, 53 ℃ of fusing points.
1H?NMR(CDCl 3，δ)：2.19ppm。
The raw material of formula (VIII)
Embodiment (VIII-1)
Figure C9811913101061
0.8g (2.36mmol) α-methoxyimino-α-[2-(2,4-dimethyl-phenoxy group-methyl)-phenyl]-Acetyl Chloride 98Min. is dissolved in the 10ml tetrahydrofuran (THF), and adds 0.26g (2.6mmol) triethylamine.0.25g (2.6mmol) O-(2-the hydroxyethyl)-azanol that will be dissolved in the 10ml tetrahydrofuran (THF) then is added dropwise under 0 ℃.Reaction mixture was stirred 2 hours at 20 ℃, pour in the water then, and use ethyl acetate extraction.The extraction solution dried over mgso concentrates the circumstances in which people get things ready for a trip spectrum (silica gel of going forward side by side; Toluene/acetone, 10: 1) handle.
Obtain 0.4g (theoretical value 50%) N-(2-hydroxyl-oxyethyl group)-α-methoxyimino-α-[2-(2,4-dimethyl-phenoxy group-methyl)-phenyl]-ethanamide.
1H?NMR(CDCl 3，δ)：3.65；3.90；9.15ppm。
The raw material of formula (XV)
Embodiment (XV-1)
Figure C9811913101071
0.93g (2.95mmol) α-methoxyimino-α-[2-(2,4-dimethyl-phenoxy group-methyl)-phenyl]-acetate is mixed with 4.0g (2.9mmol) thionyl chloride and 50mg dimethyl formamide, and mixture was stirred 30 minutes under refluxing.Distillation under reduced pressure, carefully more the evaporable component is removed.
Obtain that 0.95g α-methoxyimino-α-[2-(2,4-dimethyl-phenoxy group-methyl)-phenyl-Acetyl Chloride 98Min. is the oily residue.
Embodiment (XV-2)
Figure C9811913101081
2.0g (6.1mmol) α-methoxyimino-α-[2-(2,4-dimethyl-phenoxy group-methyl)-phenyl]-methyl acetate is dissolved in the 20ml Virahol, and adds 30ml 1N sodium hydroxide solution.Mixture was stirred 14 hours at 40 ℃, pour in the water then.With 2N hydrochloric acid its pH is transferred to 6, and the crystalline product that obtains is emanated by suction filtration.
Obtain 1.5g (theoretical value 78%) α-methoxyimino-α-[2-(2,4-dimethyl-phenoxy group-methyl)-phenyl]-acetate.
1H?NMR(CDCl 3，δ)：3.9：4.85ppm。
Purposes embodiment
Embodiment A
Net blotch of barley (Pyrenophora teres) protectiveness control test
Solvent: the N-Methyl pyrrolidone of 10 parts of weight
Emulsifying agent: the alkaryl polyglycol ether of 0.6 part of weight
During the appropriate formulation of preparation active compound,, and this missible oil is diluted with water to desired concn with the active compound of 1 part of weight and the solvent and the emulsifier mix of described amount.
Be test protectiveness activity, be sprayed onto as the dew shoot moistening with active agent preparations.After the hydrojet layer becomes dry, plant is inoculated with net blotch of barley bacterium conidial suspension.Allow plant stay in the incubator of 20 ℃ and 100% relative humidity 48 hours.
Plant is placed in the greenhouse of general 20 ℃ and relative air humidity general 80% of temperature.
Inoculating postevaluation in 7 days should test.
In this test, for example, the compound of preparation embodiment 1 demonstrates 100% prevention effect level when the amount of application of 400g/ha..
Embodiment B
The interior absorption control of the late blight of potato (Phytophthora) test
Solvent: the acetone of 4.7 parts of weight
Emulsifying agent: the alkaryl polyglycol ether of 0.3 part of weight
During the appropriate formulation of preparation active compound,, and this missible oil is diluted with water to desired concn with the active compound of 1 part of weight and the solvent and the emulsifier mix of described amount.
Be absorption energy in testing, active agent preparations poured into contained in the standard soil of preparing as the shoot of testing.Handle after 3 days, with the spore fluid suspension inoculation of phytophthora infestans.
Plant is stayed in the incubator of general 20 ℃ and 100% relative air humidity.
Inoculate after 3 days, estimate this test.
In this test, the compound that for example prepares embodiment 1 demonstrates 58% prevention effect level when activity compound concentration 100ppm.
Embodiment C
The interior absorption control of rice blast (Pyricularia) test
Solvent: the acetone of 12.5 parts of weight
Emulsifying agent: the alkaryl polyglycol ether of 0.3 part of weight
During the appropriate formulation of preparation active compound,, and the emulsifying agent of this enriched material water and described amount is diluted to desired concn with the active compound of 1 part of weight and the solvent of described amount.
For absorption energy in testing, the 40ml active agent preparations is poured in the standard soil of the rice seedlings of growing, handles after 7 days, the spore fluid suspension inoculation rice strain of usefulness Pyricularia oryzae, and it is stayed in 25 ℃ of greenhouses with relative air themperature 100%, until evaluation.
Inoculate 4 days postevaluation sickness rate.
In this test, for example, the compound of preparation embodiment 1 demonstrates 80% prevention effect level when the amount of application of 100mg/100ml.

Claims (1)

1. formula (IV) compound
Figure C981191310002C1
Wherein
The A representative has alkane two bases of 2 carbon atoms, and its optional alkyl or haloalkyl by halogen or 1 to 4 carbon atom replaces;
Ar representative optional separately phenylene or the naphthylidene that replaces, or represent 5 or 6 annular atomses, and wherein at least one annular atoms represent oxygen, sulphur or nitrogen, chooses the inferior heteroaryl that one or two other annular atoms is represented nitrogen wantonly, and wherein substituting group is selected from;
Halogen, cyano group, nitro, amino, hydroxyl, formyl radical, carboxyl, formamyl, thiocarbamoyl, respectively the do for oneself alkyl of straight or branched, alkoxyl group, alkylthio, alkyl sulphinyl or alkyl sulphonyl, they respectively have 1 to 6 carbon atom, respectively the do for oneself alkenyl of straight or branched, alkenyloxy or alkynyloxy group, they respectively have 2 to 6 carbon atoms, respectively the do for oneself haloalkyl of straight or branched, halogenated alkoxy, halogenated alkylthio, haloalkyl sulfinyl or halogenated alkyl sulfonyl, they respectively have 1 to 6 carbon atom and 1 to 13 identical or different halogen atom, respectively the do for oneself halogenated alkenyl or the halo alkenyloxy of straight or branched, they respectively have 2 to 6 carbon atoms and 1 to 13 identical or different halogen atom, respectively the do for oneself alkylamino of straight or branched, dialkyl amido, alkyl-carbonyl, alkyl carbonyl oxy, carbalkoxy, alkylsulfonyloxy, oxyimino alkyl or Alkoximino alkyl, they each at moieties separately 1 to 6 carbon atom is arranged, or representative respectively the do for oneself alkylidene group or two oxyalkylenes of divalence, they respectively have 1 to 6 carbon atom and are optionally separately replaced or polysubstituted by identical or different straight or branched alkyl that is selected from halogen and/or 1 to 4 carbon atom and/or the substituting group list that contains the straight or branched haloalkyl of 1 to 4 carbon atom and 1 to 9 identical or different halogen atom;
E represents one of following groups:
Figure C981191310003C1
Wherein
Y represents oxygen, sulphur, methylene radical or alkyl imino,
The R representative has the alkyl of 1 to 6 carbon atom,
R 1Represent hydrogen, halogen, cyano group, or represent alkyl, alkoxyl group, alkylthio, alkylamino or dialkyl amido, they respectively have 1 to 6 carbon atom and optional separately by halogen, cyano group or C on alkyl 1-C 4Alkoxyl group replaces;
R 2Represent hydrogen, amino, cyano group, or represent alkyl, alkoxyl group, alkylamino or dialkyl amido, 1 to 6 carbon atom is arranged and on their each comfortable moieties separately randomly by halogen, cyano group or C 1-C 4Alkoxyl group replaces; With
R 3Represent hydrogen, cyano group, or represent alkyl, alkenyl or alkynyl, they have maximum 6 carbon atoms and optional by halogen, cyano group or C 1-C 4Alkoxyl group replaces, or representative has 3 to 6 carbon atoms and choose cycloalkyl or the cycloalkylalkyl that 1 to 4 carbon atom is arranged at moieties wantonly at cycloalkyl moiety, they optional separately by halogen, cyano group, carboxyl, | C 1-C 4Alkyl or C 1-C 4Carbalkoxy replaces.
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EP0754684A4 (en) * 1994-04-01 1998-05-13 Shionogi & Co Oxime derivative and bactericide containing the same as active ingredient
US6268312B1 (en) 1994-04-01 2001-07-31 Shionogi & Co., Ltd. Oxime derivative and bactericide containing the same as active ingredient
SK107597A3 (en) 1995-02-13 1998-02-04 Bayer Ag Fungicidal aza-heterocycloalkenes, producing method thereof, agents for killing the pests containing the same, method of killing the pests and use said compounds
DE19602095A1 (en) * 1996-01-22 1997-07-24 Bayer Ag Halopyrimidines
TW492962B (en) 1996-05-30 2002-07-01 Bayer Ag Process for preparing 3-(1-hydroxyphenyl-1-alkoximinomethyl)dioxazines
DE19706396A1 (en) * 1996-12-09 1998-06-10 Bayer Ag Process for the preparation of 3- (l-hydroxiphenyl-l-alkoximinomethyl) dioxazines
US7521473B2 (en) 2004-02-25 2009-04-21 Wyeth Inhibitors of protein tyrosine phosphatase 1B
CA2987545C (en) * 2015-05-29 2022-08-02 Arysta Lifescience Corporation Improved process for preparing (e)-(5,6-dihydro-1,4,2-dioxazine-3-yl)(2-hydroxyphenyl)methanone o-methyl oxime

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US9193698B2 (en) 2013-07-08 2015-11-24 Advinus Therapeutics, Ltd. Process for preparing fluoxastrobin
US9670171B2 (en) 2013-07-08 2017-06-06 Arysta Lifescience Corporation Process for preparing fluoxastrobin

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