CN1486974A - New benzoyl urea compound and its synthesis and application - Google Patents

New benzoyl urea compound and its synthesis and application Download PDF

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CN1486974A
CN1486974A CNA021338728A CN02133872A CN1486974A CN 1486974 A CN1486974 A CN 1486974A CN A021338728 A CNA021338728 A CN A021338728A CN 02133872 A CN02133872 A CN 02133872A CN 1486974 A CN1486974 A CN 1486974A
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CN1228318C (en
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军 林
林军
严胜骄
杨丽娟
宗乾收
徐蓉
冒德寿
刘复初
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Yunnan University YNU
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Abstract

The synthesis process of new benzoyl urea compound includes the fluorination of chlorothalonil, the separate amination of chlorothalonil and the fluorinated product, the hydrolysis and decarboxylation of the aminated product in sulfuric acid solution to obtain compound V; the hydrolysis of compound VI in sulfuric acid solution to obtain compound VII, the reaction between compound VII and oxalyl chloride to obtain compound II; and the reaction of compound V and compound II. The benzoyl urea compound of the present invention has no halogen element in the place 4 of the phenyl group but very activity, and this has important theoretical significance. Practically, the present invention opens one new way of preparing benzoyl urea compound as insect growth regulator and the production line is short, mild in reaction condition, high in yield, low in cost and suitable for industrial production.

Description

New benzoyl urea compound and synthetic method and application
Technical field
The present invention relates to prepare new benzoyl urea compound, and this novel cpd is used to kill small cabbage moth, mythimna separata, mosquito with compound halogeno-benzene formyl isocyanic ester and compound trihalogenated benzene amine or phenyl-dihalide diamines.
Background technology
In existing phenmethyl carbamide compounds; people are by a large amount of experiments; verified its basic structure is that a compounds of N-phenyl-N '-substituted benzoyl urea has higher insecticidal activity to insect; and useful aquatic Crustachia had higher security, belong to insect growth regulator(IGR).Wherein representative has Teflubenzuron preferably.Teflubenzuron has following advantage: 1. the mechanism of action uniqueness, to the beneficial organism low toxicity, be easy to degraded, selectivity height, comparison safety, belong to insect growth regulator(IGR).2. biological activity height, effectively formulation rate is low.3. the insecticidal activity that has wide spectrum.4. there is not the transreactance of intersection with other sterilant.Its weak point is: the phenyl moiety complex structure, and difficult synthetic, the processing requirement height, thus increased overall synthetic difficulty, the cost height, uneconomical.
Summary of the invention
It is short to the purpose of this invention is to provide a kind of synthetic route, reaction conditions gentleness, the synthetic method and the application of compound (a kind of more economical more superior efficient pesticides is provided) of productive rate height, new benzoyl urea compound that synthetic route is succinct.
The phenyl moiety of benzoyl urea compound contains halogen mostly, and the kind and the insecticidal activity of the position of substitution of halogen, replacement number and halogen have substantial connection.Existing phenyl moiety commercial or that obtain benzoyl urea insecticide patent or that reported has halogen or other non-hydrogen substituting group mostly on 4.People generally believe that 4 hydrogen is active higher by replacement backs such as halogens.Though the existing report of trihalogenated benzene base, its activity is higher mostly.But this phenyl moiety is 2,3, and 5-trihalogenated benzene base or 3-amino-2, the benzoyl urea compound of 5-dihalo-phenyl do not report as yet, and this structure that our foresight tells us ... is owing to contain a plurality of halogens because of this has better, more permanent activity on the phenyl ring.The present invention is to be that lead compound carries out the structure screening and optimize having obtained the benzoyl urea compound shown in the general formula (I) with the Teflubenzuron.
The benzoyl urea compound that reaches of the present invention is represented by following general structure (I):
Wherein: R 1, R 3, R 5Be fluorine atom or chlorine atom; R 2Can be fluorine atom or amino or chlorine atom; R 4Be hydrogen, chlorine atom or fluorine atom.
This is that a class has unique effect mechanism, high environmental safety and the active compound of efficient insecticide.The present invention will address the synthesis technique of this compounds and they the indoor preventive effect test result to small cabbage moth, mythimna separata, mosquito.
Compound suc as formula the new benzoyl urea shown in (I) is prepared by following synthetic route: m-tetrachlorophthalodinitrile is carried out fluoridation production (III) compound; then m-tetrachlorophthalodinitrile and formula (III) compound are carried out amination reaction with ammonia or ammoniacal liquor respectively again; react formula (IV) compound; again formula (IV) compound is carried out the single stage method hydrolysis decarboxylation in sulphuric acid soln; two itrile groups of result are sloughed; get the formula V compound; on the other hand; with formula (VI) compound in sulphuric acid soln, be hydrolyzed react formula (VII) compound; then formula (VII) compound and oxalyl chloride are reacted formula (II) compound, again formula V compound and isocyanic ester formula (II) compound are reacted this moment new benzoyl urea compound.The structure of raw material, intermediate and target product (new benzoyl urea compound) is as follows:
The synthetic route of described formula (I) compound is (representing with structural formula):
Figure A0213387200071
Also developed the represented compound of formula (I) in addition further, the agricultural pests diamondback moth larvae has been had tangible insecticidal activity.
Gratifying example or perhaps product of the present invention are some following compounds in the benzoyl urea compound.That is:
(a) work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be H, R 5Be Cl;
(b) work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be Cl, R 5Be Cl;
(c) work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be F, R 5Be F;
(d) work as R 1Be Cl, R 2Be F, R 3During for Cl, R 4Be H, R 5Be Cl;
(e) work as R 1Be Cl, R 2Be F, R 3During for Cl, R 4Be Cl, R 5Be Cl;
(f) work as R 1Be Cl, R 2Be F, R 3During for Cl, R 4Be F, R 5Be F;
(g) work as R 1Be Cl, R 2Be F, R 3During for F, R 4Be H, R 5Be Cl;
(h) work as R 1Be Cl, R 2Be F, R 3For FThe time, R 4Be Cl, R 5Be Cl;
(i) work as R 1Be Cl, R 2Be F, R 3During for F, R 4Be F, R 5Be F;
(j) work as R 1Be F, R 2Be F, R 3During for F, R 4Be H, R 5Be Cl;
(k) work as R 1Be F, R 2Be F, R 3During for F, R 4Be Cl, R 5Be Cl;
(l) work as R 1Be F, R 2Be F, R 3During for F, R 4Be F, R 5Be F;
(m) work as R 1Be Cl, R 2Be NH 2, R 3During for Cl, R 4Be H, R 5Be Cl;
(n) work as R 1Be Cl, R 2Be NH 2, R 3During for Cl, R 4Be Cl, R 5Be Cl;
(o) work as R 1Be Cl, R 2Be NH 2, R 3During for Cl, R 4Be F, R 5Be F;
(p) work as R 1Be Cl, R 2Be NH 2, R 3During for F, R 4Be H, R 5Be Cl;
(q) work as R 1Be Cl, R 2Be NH 2, R 3During for F, R 4Be Cl, R 5Be Cl;
(r) work as R 1Be Cl, R 2Be NH 2, R 3During for F, R 4Be F, R 5Be F;
(s) work as R 1Be F, R 2Be NH 2, R 3During for F, R 4Be H, R 5Be Cl;
(t) work as R 1Be F, R 2Be NH 2, R 3During for F, R 4Be Cl, R 5Be Cl;
(u) work as R 1Be F, R 2Be NH 2, R 3During for F, R 4Be F, R 5Be F.
Wherein gratifying especially example is:
Work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be F, R 5Be F (I-1);
Work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be H, R 5Be Cl (I-2);
Work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be Cl, R 5Be Cl (I-3);
Work as R 1Be Cl, R 2Be F, R 3During for F, R 4Be F, R 5Be F (I-4);
Work as R 1Be Cl, R 2Be F, R 3During for F, R 4Be Cl, R 5Be Cl (I-5).
Work as R 1Be Cl, R 2Be F, R 3During for F, R 4Be H, R 5Be Cl (I-6).
The method that the present invention prepares benzoyl urea compound (I) relates to following steps:
Intermediate (II-1): the preparation of 2-chloro-benzoyl isocyanic ester:
Figure A0213387200081
15.5 gram (0.1mol) 2-chloro-benzamide are dissolved in are furnished with agitator, calcium chloride tube, reflux condensing tube with the hydrogen chloride gas absorption unit, dry new steaming 1, in the three-necked bottle of 2-ethylene dichloride, slowly add the new oxalyl chloride that steams of 15ml then, after the question response heat release finishes, till suspended solids all being clarified in ebuillition of heated 3-4 hour and not had hydrogenchloride and emit, at last the reaction solution underpressure distillation is removed excessive 1,2-ethylene dichloride and oxalyl chloride, obtain light yellow oily liquid 17.0 grams, productive rate 94.0% need not further be purified, seal standbyly, or be used for next step reaction immediately.
Intermediate (II-2) 2, the preparation of 6-two fluoro-benzoyl isocyanic ester:
Figure A0213387200091
With 15.7 gram (0.1mol) 2,6-two fluoro-benzamide are dissolved in is furnished with agitator, calcium chloride tube, reflux condensing tube with the hydrogen chloride gas absorption unit, dry new steaming 1, in the three-necked bottle of 2-ethylene dichloride, slowly add the new oxalyl chloride that steams of 9.5～10.5ml then, after the question response heat release finishes, till ebuillition of heated made suspended solids all clarify in 5～6 hours and does not have hydrogenchloride and emit, it is excessive 1 at last the reaction solution underpressure distillation to be removed, and 2-ethylene dichloride and oxalyl chloride obtain light yellow oily liquid 15.2 grams, productive rate 83.0%, need not further purify, seal standbyly, or be used for next step reaction immediately.
Bp：54℃(0.05mmHg)。
1HNMR(CDCl 3)：7.01(t，J＝8.3Hz，2H)，7.48-7.58(m，1H)。
Intermediate (II-3) 2, the preparation of 6-two chloro-benzoyl isocyanic ester:
Figure A0213387200092
With 18.9 gram (0.1mol) 2,6-two chloro-benzamide are dissolved in is furnished with agitator, the reflux condensing tube of calcium chloride tube and hydrogenchloride institute bulk absorption device, dry new steaming 1, in the three-necked bottle of 2-ethylene dichloride, slowly add the new oxalyl chloride that steams of 15.5～17.0ml then, after the question response heat release finishes, till ebuillition of heated made suspended solids all clarify in 20～24 hours and do not have hydrogenchloride and emit, at last the reaction solution underpressure distillation is removed excessive 1,2-ethylene dichloride and oxalyl chloride, obtain light yellow oily liquid 14.1 grams, productive rate 66.0% need not further be purified, seal standbyly, or be used for next step reaction immediately.
Intermediate (III-1) 5-chloro-2,4,6-three fluoro-1, the preparation of 3-benzene dinitrile
In 250 milliliters of three-necked bottles, add 150 milliliters of dry N that cross, dinethylformamide, add m-tetrachlorophthalodinitrile 26.6 grams (0.1mol) that drying is handled again, under mechanical stirring, being warming up to 70 ℃ dissolves it fully, add 22.0～24.0 gram (0.379～0.414mol) anhydrous potassium fluorides fast, and on the mouth of pipe of a side drying tube is installed aside, and be warming up to 110～120 ℃ of reactions then after 4～5 hours, be cooled to room temperature, remove by filter precipitation (KF+KCl), and with 30～40 milliliters of N, 2-3 above-mentioned precipitation of dinethylformamide washing (precipitating heavily about 25.2 restrains), merging filtrate, filtrate is poured in 500 ml waters, magnetic agitation half an hour, suction filtration must precipitate 11.0 grams-19.8 grams, after the drying, use the hexanaphthene recrystallization, get white needle-like crystals, nearly weigh 10.4 grams-17.2 grams (yield 48.0%～80.0%), mp:107-108 ℃. 19FNMR(acetone-d 6)：-13.35(s，2F)，-17.80(s，1F).
Intermediate (III-2) 2,4,5,6-tetrafluoro-1, the preparation of 3-benzene dinitrile
Figure A0213387200101
In 250 milliliters of three-necked bottles, add 150 milliliters of exsiccant tetramethylene sulfone, m-tetrachlorophthalodinitrile 26.6 grams (0.1mol) that add drying treatment again, under the mechanical stirring, be warming up to 70 ℃ and make it dissolve quick adding 25.0 gram anhydrous potassium fluorides fully, 0.5 gram hexaoxacyclooctadecane-6-6 is made phase-transfer catalyst, and on first the mouth of pipe drying tube is installed aside, temperature control is cooled to room temperature 160-180 ℃ of reaction 8 hours then, and overanxious place goes precipitation (KF+KCl), and with 2-3 above-mentioned precipitation of 20 milliliters of tetramethylene sulfone washing (precipitating heavily about 24.9 restrains), merging filtrate was poured in 500 ml waters filtrate into magnetic agitation 2 hours, and suction filtration must precipitate 17.6 grams, dry back selects hexanaphthene to carry out recrystallization, get white, needle-shaped crystals, get 2,4,5,6-tetrafluoro-1,3-benzene dinitrile (III-2) nearly weighs 16.4 grams (yield 70.7%).mp：102-104℃.
IR(KBr)，υmax/cm -1：2254，1642，1504，1489，1324，1131，974.
Intermediate (III-3) 2,5-two chloro-4,6-two fluoro-1, the preparation of 3-benzene dinitrile
Figure A0213387200102
In 250 milliliters of three-necked bottles, add 150 milliliters of dry N that cross, dinethylformamide, add m-tetrachlorophthalodinitrile 26.6 grams (0.1mol) that drying is handled again, under mechanical stirring, be warming up to 70 ℃ it is dissolved fully, add 14.5 gram (0.250mol) anhydrous potassium fluorides fast, and on the mouth of pipe of a side drying tube is installed aside, be warming up to 110～120 ℃ of reactions then after 2～3 hours, be cooled to room temperature, remove by filter precipitation (KF+KCl), and with 2-3 above-mentioned precipitation of 30～40 milliliters of dimethyl formamides washing, merging filtrate is poured filtrate in 500 ml waters into, magnetic agitation 1 hour, suction filtration must precipitate 12.5 grams-19.6 grams, after the drying, use the hexanaphthene recrystallization, get white solid, post separates to such an extent that white needle-like crystals nearly weighs 10.2～12.1 grams (yield 43.8%～51.9%), mp:144-147 ℃ again.
Intermediate (IV-1) 6-amino-2,4,5-three chloro-1, the preparation of 3-benzene dinitrile
26.6 gram (0.1mol) m-tetrachlorophthalodinitriles addings are furnished with agitator, in 500 milliliters of three-necked bottles of reflux condensing tube, add 250 milliliters of tetrahydrofuran (THF)s again, in 10～30 minutes ammonia is blasted in the solution.Continue down to react in 40 ℃, after finishing with TLC detection to reaction, be cooled to room temperature, after the cooling reaction solution poured in 150 ml waters and stir, suction filtration obtains white solid, after the drying, get white solid 20.1 gram (productive rate 81.5%) with re-crystallizing in ethyl acetate, mp:282～284 ℃.
MS：245(M +)(100)，218(6)，210(8)，183(14)，147(8).
Intermediate (IV-2) 6-amino-5-chloro-2,4-two fluoro-1, the preparation of 3-benzene dinitrile
With 21.6 (0.1mol) gram 5-chloro-2,4,6-three fluoro-1,3-benzene dinitrile are dissolved in 100 grams 1, the 2-methyl ethyl ether, and slowly adding 16.2 gram d under stirring in 1 hour is 0.88g/cm 225～28% ammoniacal liquor continue reaction after 2～3 hours with reaction solution afterwards, above-mentioned reaction solution is poured in 300 ml waters fully stirred, and suction filtration obtains white solid, dry 15.6 grams (productive rate 73.2%) that get of washing final vacuum.
MS：213(M +)(100)，194(2)，178(20)，159(4)，151(33)，124(15).
Intermediate (IV-3) 4,6-diamino-5-chloro-2-fluoro-1, the preparation of 3-benzene dinitrile
Figure A0213387200121
With 21.6 gram (0.1mol) 5-chloro-2,4,6-three fluoro-1,3-benzene dinitrile are dissolved in 150 grams 1, and the 2-methyl ethyl ether blasts ammonia to solution under stirring in 10 minutes.With TLC detect finish to reaction after, be cooled to room temperature, after the cooling reaction solution poured in 150 ml waters and fully stirs, suction filtration obtains white solid, the washing final vacuum dry 15.6 grams (productive rate 68.7%).
MS：210(M +)(100)，191(8)，175(36)，148(50)，121(37).
Intermediate (IV-4) 6-amino-2,4,5-three fluoro-1, the preparation of 3-benzene dinitrile
With 20 gram (0.1mol) 2,4,5,6-tetrafluoro-1,3-benzene dinitrile are dissolved in 120 grams 1, the 2-methyl ethyl ether, and slowly adding 20 gram d under stirring in 1 hour is 0.88g/cm 225～28% ammoniacal liquor continue reaction after 2～3 hours with reaction solution afterwards, above-mentioned reaction solution is poured in 150 ml waters fully stirred, and suction filtration obtains white solid, dry 11.2 grams (productive rate 56.9%) that get of washing final vacuum.
MS：197(M +)(100)，178(14)，170(65)，155(43)，139(57).
Intermediate (IV-5) 4,6-diamino-2,5-two fluoro-1, the preparation of 3-benzene dinitrile
With 20 gram (0.1mol) 2,4,5,6-tetrafluoro-1,3-benzene dinitrile dissolve in 150 grams 1, and the 2-methyl ethyl ether blasts ammonia to solution under stirring in 10 minutes.With TLC detect finish to reaction after, be cooled to room temperature, after the cooling reaction solution poured in 150 ml waters and fully stirs, suction filtration obtains white solid, the washing final vacuum dry 17.0 grams (productive rate 87.6%).
MS：194(M +)(47)，140(16)，64(100).
Intermediate (IV-6) 6-amino-2,5-two chloro-4-fluoro-1, the preparation of 3-benzene dinitrile
The same IV-2 of preparation method, productive rate 82.0%.
MS：229(M +)(100)，213(50)，194(23)，178(8)，167(25)，158(13)，
147(17).
Intermediate (IV-7) 4,6-diamino-2,5-two chloro-1, the preparation of 3-benzene dinitrile
The same IV-3 of preparation method, productive rate 52.8%.
MS：226(M +)(100)，210(48)，148(50)，121(37).
Intermediate (V-1) 2,3, the preparation of 5-three chloro-aniline
In 100 milliliters of three-necked bottles, add 24.5 gram (0.1mol) 6-amino-2,4,5-three chloro-1, the 3-benzene dinitrile adds 50 milliliter of 85% sulfuric acid again, the middle mouth of pipe is installed reflux condensing tube, the next door one side pipe mouth install thermometer, under induction stirring, be warming up to 150 ℃ the reaction 12 hours after, be cooled to room temperature after, reaction solution is poured in a large amount of ice cubes, being neutralized to PH with sodium hydroxide again is 7, after the cooling, uses dichloromethane extraction, the extraction liquid anhydrous sodium sulfate drying, methylene dichloride is removed in underpressure distillation, white solid 17.2 gram (productive rate 88.2%), mp:71～72 ℃.
MS：195(M +)(100)，160(11)，143(2)，124(30)，98(11).
Intermediate (V-2) 2-chloro-3, the preparation of 5-two fluoro-aniline
In 100 milliliters of three-necked bottles, add 21.4 gram (0.1mol) 6-amino-5-chloro-2,4-two fluoro-1, the 3-benzene dinitrile, add 40 milliliter of 75% sulfuric acid again, the middle mouth of pipe is installed reflux condensing tube, and next door one side pipe mouth is installed thermometer, under induction stirring, be warming up to 140～150 ℃ of reactions after 12 hours, after being cooled to room temperature, reaction solution is poured in a large amount of ice cubes, being neutralized to PH with sodium hydroxide again is 7, after the cooling, use dichloromethane extraction, the extraction liquid anhydrous sodium sulfate drying, methylene dichloride is removed in underpressure distillation, obtain light yellow oily liquid 13.9 grams (productive rate 85.1%)
MS：163(M +)(100)，144(1)，128(12)，108(18)，101(35).
Intermediate (V-3) 2-chloro-5-fluoro-1, the preparation of 3-phenylenediamine
Figure A0213387200133
In 100 milliliters of three-necked bottles, add 21.1 gram (0.1mol) 4,6-diamino-5-chloro-2-fluoro-1, the 3-benzene dinitrile, add 40 milliliter of 75% sulfuric acid again, the middle mouth of pipe is installed reflux condensing tube, and next door one side pipe mouth is installed thermometer, is warming up to 140～150 ℃ of reactions after 12 hours under induction stirring, after being cooled to room temperature, reaction solution is poured in a large amount of ice cubes, and being neutralized to PH with sodium hydroxide again is 7, after the cooling, use dichloromethane extraction, the extraction liquid anhydrous sodium sulfate drying, methylene dichloride is removed in underpressure distillation, gets white solid 12.5 grams (productive rate 78.5%).
MS：160(M +)(100)，143(7)，132(23)，123(13)，98(58).
Intermediate (V-4) 2,3, the preparation of 5-trifluoromethyl aniline
The same V-2 of preparation method, productive rate gets 86.0%.
GC/MS：147(M +)(100)
Intermediate (V-5) 2,5-two fluoro-1, the preparation of 3-phenylenediamine
The same V-3 of preparation method, productive rate gets 77.6%.
GC/MS：144(M +)(100)
Intermediate (V-6) 2, the preparation of 5-two chloro-3-fluoroanilines
The same V-2 of preparation method, productive rate gets 84.2%.
MS：179(M +)(100)，144(16)，124(6)，117(27)，108(33).
Intermediate (V-7) 2,5-two chloro-1, the preparation of 3-phenylenediamine
The same V-3 of preparation method, productive rate gets 70.2%.
GC/MS：176(M +)(100)
The preparation of intermediate (VII-1) 2-chloro-benzamide
With 2-chloro-benzene nitrile 13.7 gram (0.1mol) and concentration is that 98% sulfuric acid joins in 50 milliliters of three-necked bottles for 15 milliliters, and 45-50 ℃ of stirring reaction 2 hours, when being cooled to 20 ℃, being neutralized to PH with NaOH then was 7, cooling, the Na of water flush away absorption 2SO 4, the infrared lamp drying is used DMF-H 2The O recrystallization gets white powdery solid 12.4 gram (productive rates 80%) .mp:138-142 ℃.
1HNMR(δ H，，ppm)：7.91(1H，s，br)，7.61(1H，s，br)，7.3-7.5(4H，m).
Intermediate (VII-2) 2, the preparation of 6-two fluoro-benzamide
With 2,6-two fluoro-benzene nitriles 13.9 grams (0.1mol) and concentration are that 98% sulfuric acid joins in 100 milliliters of three-necked bottles for 20 milliliters, and 65-70 ℃ of stirring reaction 2.5 hours, when being cooled to 20 ℃, being neutralized to PH with NaOH then was 7, cooling, the Na of water flush away absorption 2SO 4, the infrared lamp drying is used DMF-H 2The O recrystallization gets white powdery solid 13.5 gram (productive rates 85.9%) .mp:143-148 ℃.
1HNMR(δ H，，ppm)：8.15(1H，s，br)，7.85(1H，s，br)，7.5(1H，m)，7.15
(2H，t).
Intermediate (VII-3) 2, the preparation of 6-two chloro-benzamide
With 2,6-two chloro-benzene nitriles 17.2 grams (0.1mol) and concentration are that 98% sulfuric acid joins in 100 milliliters of three-necked bottles for 25 milliliters, and 75-80 ℃ of stirring reaction 3 hours, when being cooled to 20 ℃, being neutralized to PH with NaOH then was 7, cooling, the Na of water flush away absorption 2SO 4, the infrared lamp drying is used DMF-H 2The O recrystallization gets white powdery solid 16.5 gram (productive rates 86.8%) .mp:193-197 ℃.
1HNMR(δ H，，ppm)：8.10(1H，s，br)，7.80(1H，s，br)，7.3-7.6(3H，m).
The preparation of compound of the present invention
M-tetrachlorophthalodinitrile is carried out fluoridation production (III) compound; then m-tetrachlorophthalodinitrile and formula (III) compound are carried out amination reaction with ammonia or ammoniacal liquor respectively again; react formula (IV) compound; again formula (IV) compound is carried out the single stage method hydrolysis decarboxylation in sulphuric acid soln and get the formula V compound; on the other hand; with formula (VI) compound in sulphuric acid soln, be hydrolyzed react formula (VII) compound; then formula (VII) compound and oxalyl chloride are reacted formula (II) compound, again formula V compound and isocyanic ester formula (II) compound are reacted this moment the new benzoyl urea compound shown in the formula (I).
M-tetrachlorophthalodinitrile carries out the fluorine permutoid reaction with KF, and Cl is exchanged by F, and exchange can only be in the O-or the P-position of CN base, and the result obtains formula (III) compound, and m-tetrachlorophthalodinitrile and formula (III) compound re-uses NH respectively 3Or NH 3H 2O carries out amination reaction, can only be on the O-or P-position of CN base, can one or two F or a chlorine by amination, obtain formula (IV) compound, (IV) compound single stage method hydrolysis decarboxylation in sulphuric acid soln again, two itrile groups of result are hydrolyzed to be taken off, the formula V compound.On the other hand, with formula (VI) compound in sulphuric acid soln, be hydrolyzed react formula (VII) compound, then formula (VII) compound and oxalyl chloride are reacted formula (II) compound.Again will (V) formula react this moment and obtain formula (I) compound with (II) compound.It is existing that details are as follows:
1) m-tetrachlorophthalodinitrile reacts with KF, and processing condition are relatively gentleer, and yield is good.Can be exchanged by F at the O-of CN base or the Cl on the P-position.Little and the bigger surface-area of the best granularity of used KF should be removed end drying.Solvent is a non-protonic solvent as DMF, DMSO, tetramethylene sulfone etc.Can consider with catalyzer as the case may be, as 18-C-6, n-hexadecyl trimethylammonium bromide.
Consumption: to 1 mole of m-tetrachlorophthalodinitrile, when 2 Cl were replaced by F, the consumption of KF was the 2.0-3.0 mole; Quantity of solvent is the 1-10 mole; Catalytic amount is the 0.005-0.2 mole.To 1 mole of m-tetrachlorophthalodinitrile, when 3 Cl were replaced by F, the consumption of KF was the 3.2-4.5 mole; Quantity of solvent is the 1-10 mole; Catalytic amount is the 0.005-0.2 mole.To 1 mole of m-tetrachlorophthalodinitrile, when 4 Cl were replaced by F, the consumption of KF was the 4.0-7.0 mole; Quantity of solvent is the 1-10 mole; Catalytic amount is the 0.005-0.2 mole.
Temperature of reaction: do not make concrete regulation, be generally 100-220 ℃.
Reaction times: do not make concrete regulation, be generally 1-10 hour.
Productive rate: do not do clearly regulation, be generally 43-80%.
2) amination reaction
Formula (III) compound and NH 3Or NH 3H 2O carries out amination reaction, can only be on the O-or P-position of CN base, can one or two F by amination; Direct and the NH of m-tetrachlorophthalodinitrile 3Or NH 3H 2O carries out amination reaction, can only be on the O-or P-position of CN base, can a Cl by amination.Reaction is thermopositive reaction, but also relatively gentleer, accomplishes easily, can use the ammoniacal liquor of ammonia or 28-30%, accomplishes easily.The result has generated formula (IV) compound.The solvent that uses can be selected as required, as: glycol dimethyl ether, THF, DMF, 95% ethanol, toluene, acetonitrile etc.
Consumption: to 1 mole (III), NH 3Or NH 3H 2O often is the 1-20 mole, but does not make concrete regulation.
Solvent load: not doing clearly regulation, generally is a (III) compound 1-10 part solvent.
Temperature of reaction: do not do clearly regulation, be generally-30-60 ℃, be preferably in-10 ℃-room temperature.
Reaction times: do not do clearly regulation, be generally 2-8 hour.
Yield: 52-88%.
Purity: 98%.
3) hydrolysis decarboxylation
Formula (IV) compound and the vitriol oil react, and two itrile groups are sloughed simultaneously.Use the sulphuric acid soln of solvent as 60-85%.The result has generated the formula V compound.
Consumption: to 1 mole (IV), sulfuric acid is the 5-15 mole.But do not make concrete regulation.
Temperature: do not make concrete regulation.Normal is 130-160 ℃.
Reaction times: do not make concrete regulation.But it often is 2-12 hour.
Yield: do not make concrete regulation.But often be 70-88%.
Purity: 98%.
4) hydrolysis of adjacent halogenated benzonitrile
Formula (VI) compound and the vitriol oil react, and thalidomide is stayed the acid amides stage, and the result has generated formula (VII) compound.Use the sulphuric acid soln of solvent as 85-98%.Often be 98% sulfuric acid.
Consumption: to 1 mole (VI), sulfuric acid is the 2-10 mole.But do not make concrete regulation.
Temperature: do not make concrete regulation.Normal is 20-100 ℃.
Reaction times: do not make concrete regulation.But it often is 2-12 hour.
Yield: do not make concrete regulation.But often be 80-87%.
Purity: 98%.
5) isocyanation esterification of benzamide reaction
Formula (VII) compound and oxalyl chloride react formula (II) compound, using solvent is that non-matter solvent is as (1,2-ethylene dichloride, toluene etc.).
Consumption: to 1 mole (VII), oxalyl chloride is the 1-3 mole.But do not make concrete regulation.
Solvent load: not doing clearly regulation, generally is a (VII) compound 1-10 part solvent.
Temperature: do not make concrete regulation.Normal is 0-100 ℃.
Reaction times: do not make concrete regulation.But it often is 3-24 hour.
Yield: do not make concrete regulation.But often be 66-94%.
Purity: 98%.
6) acylation reaction
Formula (II) compound and formula V carry out acylation reaction, use solvent can select as required as ethylene dichloride, trichloromethane, toluene etc.
Consumption:, (V) be the 1.0-1.3 mole to 1 mole (II).
Solvent load: not doing clearly regulation, generally is that a (II) uses 2-10 part solvent.
Temperature: do not make concrete regulation.Be generally-10-140 ℃.
Reaction times: do not do clearly regulation, be generally 5-24 hour.
Yield: more than 90%.
Purity: 98%.
The present invention has following positively effect compared with the prior art:
The present invention selects for use the raw material m-tetrachlorophthalodinitrile (2,4,5,6-tetrachloro-1,3-benzene dinitrile) that is easy to get with a kind of Yunnan as the starting raw material of phenyl moiety, its structure is modified synthetic, obtains a series of brand-new benzoylureas analog derivatives.Novelty of the present invention is 4 halogen of phenyl.It give birth to be surveyed result and shows, and is active same even higher, and this is significant aspect theoretical.Aspect practice, opened up the practical route of a preparation benzoylureas.And synthetic route is short, the reaction conditions gentleness, and the productive rate height, special suitability for industrialized production, cost is low.Because the benzoylureas analog derivative has been introduced fungicide chlorothalonil as parent, therefore, compares with known similar compound, has higher desinsection ovicidal action; Again owing to fish and Mammals there being low toxicity extremely reduced harm to environment, therefore it can eradicate or stop house pest, the parasitic insect of animals and plants and injurious forest-insect effectively, experimental results show that it has insecticidal action efficiently, particularly the restraining effect of casting off a skin to larva is more effective.Its method is insect directly to be contacted or absorb compound of the present invention to get final product.In entire production process, have that raw material is easy to get, synthetic route is succinct, easy and simple to handle, a advantage that productive rate is high, reduce the people's livelihood greatly and produce cost, be particularly suitable for industrialized developing.
Embodiment
Embodiment 1:
Produce N-(2, the 6-difluoro benzoyl)-N '-(2,3, the 5-trichlorophenyl) urea: take by weighing 0.1 mole of benzoyl isocyanic ester (II-2) of preparation just, with drying 1, the 2-ethylene dichloride makes its dissolved dilution in being furnished with the flask of agitator; Other takes by weighing 0.1 mole anils V-1, also use exsiccant 1, the 2-ethylene dichloride makes it be dissolved into solution, stir then slowly to drip to down and above-mentionedly separate out white solid immediately with ice cube refrigerative reaction flask, treat that heat release finishes after, room temperature continued reaction after 3～4 hours, reflux water 1 hour, cooling, suction filtration gets solid.Get white, needle-shaped crystals body N-(2, the 6-difluoro benzoyl)-N '-(2,3, the 5-trichlorophenyl) urea (I-1) 35.2 grams, productive rate 92.6% with re-crystallizing in ethyl acetate.
Embodiment 2:
Produce N-(2-chlorobenzene formacyl)-N '-(2,3, the 5-trichlorophenyl) urea: take by weighing 0.1 mole of benzoyl isocyanic ester (II-1) of preparation just, with drying 1, the 2-ethylene dichloride makes its dissolved dilution in being furnished with the flask of agitator; Other takes by weighing 0.1 mole anils V-1, also use exsiccant 1, the 2-ethylene dichloride makes it be dissolved into solution, stir then slowly to drip to down and above-mentionedly separate out white solid immediately with ice cube refrigerative reaction flask, treat that heat release finishes after, room temperature continued reaction after 3～4 hours, reflux water 1 hour, cooling, suction filtration gets solid.Get white, needle-shaped crystals body N-(2-chlorobenzene formacyl)-N '-(2,3, the 5-trichlorophenyl) urea (I-2) 34.7 grams, productive rate 91.8% with re-crystallizing in ethyl acetate.
Embodiment 3:
Produce N-(2,6-dichloro-benzoyl base)-N '-(2,3, the 5-trichlorophenyl) urea: take by weighing 0.1 mole of benzoyl isocyanic ester (II-3) of preparation just, with drying 1, the 2-ethylene dichloride makes its dissolved dilution in being furnished with the flask of agitator; Other takes by weighing 0.1 mole anils V-1, also use exsiccant 1, the 2-ethylene dichloride makes it be dissolved into solution, stir then slowly to drip to down and above-mentionedly separate out white solid immediately with ice cube refrigerative reaction flask, treat that heat release finishes after, room temperature continued reaction after 3～4 hours, reflux water 1 hour, cooling, suction filtration gets solid.Get white, needle-shaped crystals body N-(2,6-dichloro-benzoyl base)-N '-(2,3, the 5-trichlorophenyl) urea (I-3) 37.4 grams, productive rate 90.7% with re-crystallizing in ethyl acetate.
Embodiment 4:
Produce N-(2, the 6-difluoro benzoyl)-N '-(2-chloro-3,5-difluorophenyl) urea: take by weighing 0.1 mole of benzoyl isocyanic ester (II-2) of preparation just, with drying 1, the 2-ethylene dichloride makes its dissolved dilution in being furnished with the flask of agitator; Other takes by weighing 0.11 mole anils V-2, also use exsiccant 1, the 2-ethylene dichloride makes it be dissolved into solution, stir then slowly to drip to down and above-mentionedly separate out white solid immediately with ice cube refrigerative reaction flask, treat that heat release finishes after, room temperature continued reaction after 3～4 hours, reflux water 1 hour, cooling, suction filtration gets solid.Get white, needle-shaped crystals body N-(2, the 6-difluoro benzoyl)-N '-(2-chloro-3,5-difluorophenyl) urea (I-4) 32.1 grams, productive rate 92.6% with re-crystallizing in ethyl acetate.
Embodiment 5:
Produce N-(2,6-dichloro-benzoyl base)-N '-(2-chloro-3,5-difluorophenyl) urea: take by weighing 0.1 mole of benzoyl isocyanic ester (II-3) of preparation just, with drying 1, the 2-ethylene dichloride makes its dissolved dilution in being furnished with the flask of agitator; Other takes by weighing 0.11 mole anils V-2, also use exsiccant 1, the 2-ethylene dichloride makes it be dissolved into solution, stir then slowly to drip to down and above-mentionedly separate out white solid immediately with ice cube refrigerative reaction flask, treat that heat release finishes after, room temperature continued reaction after 3～4 hours, reflux water 1 hour, cooling, suction filtration gets solid.Get white, needle-shaped crystals body N-(2,6-dichloro-benzoyl base)-N '-(2-chloro-3,5-difluorophenyl) urea (I-5) 34.2 grams, productive rate 90.1% with re-crystallizing in ethyl acetate.
Embodiment 6:
Produce N-(2-chlorobenzene formacyl)-N '-(2-chloro-3,5-difluorophenyl) urea: take by weighing 0.1 mole of benzoyl isocyanic ester (II-1) of preparation just, with drying 1, the 2-ethylene dichloride makes its dissolved dilution in being furnished with the flask of agitator; Other takes by weighing 0.1 mole anils V-2, also use exsiccant 1, the 2-ethylene dichloride makes it be dissolved into solution, stir then slowly to drip to down and above-mentionedly separate out white solid immediately with ice cube refrigerative reaction flask, treat that heat release finishes after, room temperature continued reaction after 3～4 hours, reflux water 1 hour, cooling, suction filtration gets solid.Get white, needle-shaped crystals body N-(2-chlorobenzene formacyl)-N '-(2-chloro-3,5-difluorophenyl) urea (I-6) 32.6 grams, productive rate 94.5% with re-crystallizing in ethyl acetate.
The insecticidal effect of benzoyl urea compound preparation is described with the indoor desinsection drug effect example that contains the benzoyl urea compound preparation below.
(1). benzoyl urea compound (I) is to the prevention effect of diamondback moth larvae
Embodiment 1:
Benzoyl urea compound (I-1) preparation is diluted to 100ppm; 50ppm; 10ppm makes concentration and handles; the object crop is the wild cabbage of group's phase; for examination worm source is small cabbage moth 1-2 instar larvae, adopts leaf dish method, and each concentration is done four repetitions. behind medicine 3 days; 5 days, investigated diamondback moth larvae survival number in 7 days respectively.Add up four reproducible results and average.Drug effect result shows: after benzoyl urea compound (I-1) the 100ppm dispenser 3 days, mortality ratio was 51.3%.After the dispenser 5 days, mortality ratio was 97.4%.After the dispenser 7 days, mortality ratio was 100.0%; After the 50ppm dispenser 3 days, mortality ratio was 50.3%.After the dispenser 5 days, mortality ratio was 97.4%.After the dispenser 7 days, mortality ratio was 100.0%; After the 10ppm dispenser 3 days, mortality ratio was 48.7%.After the dispenser 5 days, mortality ratio was 89.7%.After the dispenser 7 days, mortality ratio was 100.0%.
Embodiment 2:
Benzoyl urea compound (I-2) preparation is diluted to 100ppm, and 50ppm, 10ppm make concentration and handle, and the object crop is the wild cabbage of group's phase, are small cabbage moth 1-2 instar larvae for examination worm source, adopt leaf dish method, and each concentration is done four repetitions.Behind medicine 3 days, 5 days, investigated diamondback moth larvae survival number in 7 days respectively.Add up four reproducible results and average.Drug effect result shows: after benzoyl urea compound (I-2) the 100ppm dispenser 3 days, mortality ratio was 72.9%.After the dispenser 5 days, mortality ratio was 97.1%.After the dispenser 7 days, mortality ratio was 100.0%; After the 50ppm dispenser 3 days, mortality ratio was 73.0%.After the dispenser 5 days, mortality ratio was 97.6%.After the dispenser 7 days, mortality ratio was 100.0%; After the 10ppm dispenser 3 days, mortality ratio was 73.0%.After the dispenser 5 days, mortality ratio was 90.4%.After the dispenser 7 days, mortality ratio was 100.0%.
Embodiment 3:
Benzoyl urea compound (I-3) preparation is diluted to 100ppm, and 50ppm, 10ppm make concentration and handle, and the object crop is the wild cabbage of group's phase, are small cabbage moth 1-2 instar larvae for examination worm source, adopt leaf dish method, and each concentration is done four repetitions.Behind medicine 3 days, 5 days, investigated diamondback moth larvae survival number in 7 days respectively.Add up four reproducible results and average.Drug effect result shows: after benzoyl urea compound (I-3) the 100ppm dispenser 3 days, mortality ratio was 51.3%.After the dispenser 5 days, mortality ratio was 97.4%.After the dispenser 7 days, mortality ratio was 100.0%; After the 50ppm dispenser 3 days, mortality ratio was 51.2%.After the dispenser 5 days, mortality ratio was 92.1%.After the dispenser 7 days, mortality ratio was 100.0%; After the 10ppm dispenser 3 days, mortality ratio was 51.3%.After the dispenser 5 days, mortality ratio was 97.4%.After the dispenser 7 days, mortality ratio was 100.0%.
Embodiment 4:
Benzoyl urea compound (I-4) preparation is diluted to 100ppm, and 50ppm, 10ppm make concentration and handle, and the object crop is the wild cabbage of group's phase, are small cabbage moth 1-2 instar larvae for examination worm source, adopt leaf dish method, and each concentration is done four repetitions.Behind medicine 3 days, 5 days, investigated diamondback moth larvae survival number in 7 days respectively.Add up four reproducible results and average.Drug effect result shows: after benzoyl urea compound (I-6) the 100ppm dispenser 3 days, mortality ratio was 52.0%.After the dispenser 5 days, mortality ratio was 94.9%.After the dispenser 7 days, mortality ratio was 97.6%; After the 50ppm dispenser 3 days, mortality ratio was 20.5%.After the dispenser 5 days, mortality ratio was 89.5%.After the dispenser 7 days, mortality ratio was 97.3%; After the 10ppm dispenser 3 days, mortality ratio was 17.9%.After the dispenser 5 days, mortality ratio was 78.8%.After the dispenser 7 days, mortality ratio was 97.1%.
(2) benzoyl urea compound (I) is to gluing the toxic action of larva:
Embodiment 1:
(I-1) become the solution of 200ppm concentration with acetone solution, again according to insecticidal effect with the rare one-tenth desired concn of acetone.The object crop is the leaf of Semen Maydis in seedling stage, for examination worm source be 4 age mythimna separata, adopt leaf dipping method, 24 hours, 48 hours, 72 hours, 96 hours, viewing test result add the fresh corn blade at any time behind medicine, become for 5 ages until the normal decortication of control larvae.Armyworm larvae is dead fully, and that promptly touches motionlessly is the larva death standard.Drug effect result shows: benzoyl urea compound (I-1) 200ppm mortality ratio is 100%; The 100ppm mortality ratio is 100%; The 50ppm mortality ratio is 100%; The 10ppm mortality ratio is 100%; The 5ppm mortality ratio is 95%, and the 2.5ppm mortality ratio is 80%.
Embodiment 2:
(I-2) become the solution of 200ppm concentration with acetone solution, again according to insecticidal effect with the rare one-tenth desired concn of acetone.The object crop is the leaf of Semen Maydis in seedling stage, for examination worm source be 4 age mythimna separata, adopt leaf dipping method, 24 hours, 48 hours, 72 hours, 96 hours, viewing test result add the fresh corn blade at any time behind medicine, become for 5 ages until the normal decortication of control larvae.Armyworm larvae is dead fully, and that promptly touches motionlessly is the larva death standard.Drug effect result shows: benzoyl urea compound (I-2) 200ppm mortality ratio is 100%; The 100ppm mortality ratio is 100%; The 50ppm mortality ratio is 95%; The 10ppm mortality ratio is 85%; The 5ppm mortality ratio is 65%.
Embodiment 3:
(I-3) become the solution of 200ppm concentration with acetone solution, again according to insecticidal effect with the rare one-tenth desired concn of acetone.The object crop is the leaf of Semen Maydis in seedling stage, for examination worm source be 4 age mythimna separata, adopt leaf dipping method, 24 hours, 48 hours, 72 hours, 96 hours, viewing test result add the fresh corn blade at any time behind medicine, become for 5 ages until the normal decortication of control larvae.Armyworm larvae is dead fully, and that promptly touches motionlessly is the larva death standard.Drug effect result shows: benzoyl urea compound (I-3) 200ppm mortality ratio is 100%; The 100ppm mortality ratio is 100%; The 50ppm mortality ratio is 100%; The 10ppm mortality ratio is 75%.
Embodiment 4:
(I-4) become the solution of 200ppm concentration with acetone solution, again according to insecticidal effect with the rare one-tenth desired concn of acetone.The object crop is the leaf of Semen Maydis in seedling stage, for examination worm source be 4 age mythimna separata, adopt leaf dipping method, 24 hours, 48 hours, 72 hours, 96 hours, viewing test result add the fresh corn blade at any time behind medicine, become for 5 ages until the normal decortication of control larvae.Armyworm larvae is dead fully, and that promptly touches motionlessly is the larva death standard.Drug effect result shows: benzoyl urea compound (I-4) 200ppm mortality ratio is 100%; The 100ppm mortality ratio is 90%.
Embodiment 5:
(I-5) become the solution of 200ppm concentration with acetone solution, again according to insecticidal effect with the rare one-tenth desired concn of acetone.The object crop is the leaf of Semen Maydis in seedling stage, for examination worm source be 4 age mythimna separata, adopt leaf dipping method, 24 hours, 48 hours, 72 hours, 96 hours, viewing test result add the fresh corn blade at any time behind medicine, become for 5 ages until the normal decortication of control larvae.Armyworm larvae is dead fully, and that promptly touches motionlessly is the larva death standard.Drug effect result shows: benzoyl urea compound (I-5) 200ppm mortality ratio is 100%; The 100ppm mortality ratio is 100%; The 50ppm mortality ratio is 95%.
Embodiment 6:
(I-6) become the solution of 200ppm concentration with acetone solution, again according to insecticidal effect with the rare one-tenth desired concn of acetone.The object crop is the leaf of Semen Maydis in seedling stage, for examination worm source be 4 age mythimna separata, adopt leaf dipping method, 24 hours, 48 hours, 72 hours, 96 hours, viewing test result add the fresh corn blade at any time behind medicine, become for 5 ages until the normal decortication of control larvae.Armyworm larvae is dead fully, and that promptly touches motionlessly is the larva death standard.Drug effect result shows: benzoyl urea compound (I-6) 200ppm mortality ratio is 100%; The 100ppm mortality ratio is 100%; The 50ppm mortality ratio is 95%.
(3) benzoyl urea compound (I) is to the toxic action of mosquito larvae
Embodiment 1:
Mythimna separata is adopted leaf dipping method, and benzoyl urea compound (I-1) sample is mixed with the solution of 5ppm concentration with acetone solution, becomes desired concn according to insecticidal effect with acetone diluted again.Dipping leaf of Semen Maydis in seedling stage is put into the 7cm culture dish after drying, insert 10 of 4 instar larvaes, and every concentration repeats 2 times ~ 4 times.Contrast acetone soln soaking maize leaf breeding grub.Take out the processing blade that larva does not eat up after 24 hours, add fresh maize leaf.Later 24 hours, 48 hours, 72 hours, 96 hours viewing test results add the fresh corn blade at any time, become for 5 ages until the normal decortication of control larvae.Dead fully with armyworm larvae, that is: that touches motionlessly is the death standard of larva.When concentration was 0.05ppm, mortality ratio was 100%; When concentration was 0.005ppm, mortality ratio was 100%; 0.001ppm the time, mortality ratio is 100%.
Embodiment 2:
Mythimna separata is adopted leaf dipping method, and benzoyl urea compound (I-2) sample is mixed with the solution of 5ppm concentration with acetone solution, becomes desired concn according to insecticidal effect with acetone diluted again.Dipping leaf of Semen Maydis in seedling stage is put into the 7cm culture dish after drying, insert 10 of 4 instar larvaes, and every concentration repeats 2 times ~ 4 times.Contrast acetone soln soaking maize leaf breeding grub.Take out the processing blade that larva does not eat up after 24 hours, add fresh maize leaf.Later 24 hours, 48 hours, 72 hours, 96 hours viewing test results add the fresh corn blade at any time, become for 5 ages until the normal decortication of control larvae.Dead fully with armyworm larvae, that promptly touches motionlessly is the death standard of larva.When concentration was 0.05ppm, mortality ratio was 100%; When concentration was 0.005ppm, mortality ratio was 100%; When concentration was 0.001ppm, mortality ratio was 100%.

Claims (7)

1, a kind of new benzoyl urea compound is characterized in that its structural formula is as follows:
Figure A0213387200021
In the formula, radicals R 1, R 3, R 5Can be fluorine atom or chlorine atom; R 2Can be fluorine atom or chlorine atom or amino; R 4Can be hydrogen atom, chlorine atom or fluorine atom.
2. the synthetic method of formula according to claim 1 (I) compound, it is characterized in that m-tetrachlorophthalodinitrile is carried out fluoridation production (III) compound, then m-tetrachlorophthalodinitrile and formula (III) compound are carried out amination reaction with ammonia or ammoniacal liquor respectively again, react formula (IV) compound, again formula (IV) compound is carried out the single stage method hydrolysis decarboxylation in sulphuric acid soln, two itrile groups of result are sloughed, and get the formula V compound; On the other hand; with in sulphuric acid soln, the be hydrolyzed reaction and rest on the acid amides stage of formula (VI) compound; get formula (VII) compound; then formula (VII) compound and oxalyl chloride are reacted formula (II) compound, again formula V compound and isocyanic ester formula (II) compound are reacted this moment formula (I) new benzoyl urea compound.
3. the described synthetic method of root a tree name claim 2 is characterized in that the synthetic route of formula (I) compound is:
4, according to claim 2 or 3 described synthetic methods, it is characterized in that m-tetrachlorophthalodinitrile carries out the fluorine permutoid reaction with KF, Cl is exchanged by F, and exchange can only be in the O-or the P-position of CN base, and the result obtains formula (III) compound, and m-tetrachlorophthalodinitrile and formula (III) compound is used NH respectively again 3Or NH 3.H 2O carries out amination reaction, can only be on the O-or P-position of CN base, can one or two F or a chlorine by amination, obtain formula (IV) compound, (IV) compound single stage method hydrolysis decarboxylation in sulphuric acid soln again, two itrile groups of result are hydrolyzed to be taken off, the formula V compound.
5, compound according to claim 1 is characterized in that general structure is
Compound as follows:
(a) work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be H, R 5Be Cl;
(b) work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be Cl, R 5Be Cl;
(c) work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be F, R 5Be F;
(d) work as R 1Be Cl, R 2Be F, R 3During for Cl, R 4Be H, R 5Be Cl;
(e) work as R 1Be Cl, R 2Be F, R 3During for Cl, R 4Be Cl, R 5Be Cl;
(f) work as R 1Be Cl, R 2Be F, R 3During for Cl, R 4Be F, R 5Be F;
(g) work as R 1Be Cl, R 2For F, R 3During for F, R 4Be H, R 5Be Cl;
(h) work as R 1Be Cl, R 2Be F, R 3During for F, R 4Be Cl, R 5Be Cl;
(i) work as R 1Be Cl, R 2Be F, R 3During for F, R 4Be F, R 5Be F;
(j) work as R 1Be F, R 2Be F, R 3During for F, R 4Be H, R 5Be Cl;
(k) work as R 1Be F, R 2Be F, R 3During for F, R 4Be Cl, R 5Be Cl;
(l) work as R 1Be F, R 2Be F, R 3During for F, R 4Be F, R 5Be F;
(m) work as R 1Be Cl, R 2Be NH 2, R 3During for Cl, R 4Be H, R 5Be Cl;
(n) work as R 1Be Cl, R 2Be NH 2, R 3During for Cl, R 4Be Cl, R 5Be Cl;
(o) work as R 1Be Cl, R 2Be NH 2, R 3During for Cl, R 4Be F, R 5Be F;
(p) work as R 1Be Cl, R 2Be NH 2, R 3During for F, R 4Be H, R 5Be Cl;
(q) work as R 1Be Cl, R 2Be NH 2, R 3During for F, R 4Be Cl, R 5Be Cl;
(r) work as R 1Be Cl, R 2Be NH 2, R 3During for F, R 4Be F, R 5Be F;
(s) work as R 1Be F, R 2Be NH 2, R 3During for F, R 4Be H, R 5Be Cl;
(t) work as R 1Be F, R 2Be NH 2, R 3During for F, R 4Be Cl, R 5Be Cl;
(u) work as R 1Be F, R 2Be NH 2, R 3During for F, R 4Be F, R 5Be F.
6, compound according to claim 1 is characterized in that the compound of said structure general formula is:
Work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be F, R 5Be F;
Work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be H, R 5Be Cl;
Work as R 1Be Cl, R 2Be Cl, R 3During for Cl, R 4Be Cl, R 5Be Cl;
Work as R 1Be Cl, R 2Be F, R 3During for Cl, R 4Be F, R 5Be F;
Work as R 1Be Cl, R 2Be F, R 3During for F, R 4Be F, R 5Be F;
Work as R 1Be F, R 2Be F, R 3During for F, R 4Be H, R 5Be Cl;
Work as R 1Be F, R 2Be NH 2, R 3During for F, R 4Be Cl, R 5Be Cl.
7, the sterilant of compound benzoyl urea compound according to claim 1 is characterized in that: R wherein 1, R 3, R 5Be fluorine atom or chlorine atom; R 2Be fluorine atom or amino or chlorine atom; R 4Can be hydrogen atom or chlorine atom or fluorine atom.
CN 02133872 2002-09-30 2002-09-30 New benzoyl urea compound and its synthesis and application Expired - Fee Related CN1228318C (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100369893C (en) * 2005-01-27 2008-02-20 唐烃 Production of o-chlor-benzoylurea from tobacco stalks

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100369893C (en) * 2005-01-27 2008-02-20 唐烃 Production of o-chlor-benzoylurea from tobacco stalks

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