TW200800021A - Pest-controlling agent and a method for using the same - Google Patents

Abstract

To provide a pest-controlling agent comprising at least one compound selected from a substituted aminoquinazolinone compound and salts thereof represented by general formula(1) (wherein, R represents hydrogen atom, (C1-C6)) alkylcarbonyl, (C1-C6) alkoxycarbonyl, (C1-C6)alkoxycarbonyl(C1-C3)alkyl, R1 represents pyridyl and the like, Z represents-N(R3)-CH(R2)-(in formula, R2 represents a hydrogen atom or (C1-C6)alkyl and the like, R3 represents a hydrogen atom or(C1-C6)alkyl and the like), each X is same or different, and represents bromine atom, halo (C1-C8)alkyl, halo(C1-C6)alkoxy, halo(C1-C6)alkylthio and the like, n represents an integral of 1 to 4, and at least one compound selected from a compound having insecticidal, acaricidal, or nematocidal activity, as effective ingredient, and a method for using the same.

Description

200800021, IX1 invention description: - - - - - [Technical field of the invention] The present invention relates to a substituted aminoquinazolinone compound or the like thereof, which is used as an insecticide or a sizing agent A salt, and a pest control agent capable of exerting a synergistic effect and a method for using the same, which comprises a compound selected from the group consisting of insecticidal activity, acaricidal activity or nematicidal activity, or a compound of 2' or more. VIII [Prior Art] The substituted amino quinazolinone compound which is an active ingredient of the pest control agent of the present invention is a known compound which has been described as having insecticidal activity or nematicidal activity (for example, refer to Patent Documents and 2, In particular, reference is made to Patent Document 2). Further, compounds having insecticidal activity, acaricidal activity or nematicidal activity are known in the literature, respectively (for example, refer to Non-Patent Document i, Patent Document 3), and Patent Document 4 discloses a substituted aminoquinazolinone. (thione) 10 derivatives and compounds having insecticidal or acaricidal activity provide pest control. Japanese Patent Laid-Open Publication No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. 2〇〇1_64107 Bulletin Non-Patent Document 1 · The Pesticide Manual 13th Edition, 2003 [Invention Content] 318305 5 200800021 "(The subject of the invention) ------------ ------------------------------ The object of the present invention is to provide a substituted amino quinazolinone compound or insecticidal activity, respectively. , a compound of acaricidal activity or nematicidal activity, a pest control agent which is impossible to control or difficult to control, and a method for using the same. (Means for Solving the Problem) In order to solve the above problem, the inventors of the present invention have tried to reproduce the results of the above-mentioned 'the following general formula (1) substituted amino quinazolinone compound 10, wherein, in particular, _3,4•Dihydroxy-3_[(3_pyridylmethyl)amino]-6_[1,2,2,2-tetrafluoro·ι_(trifluoromethyl)ethyl](1H)_quin Oxazolinone, and one or more compounds selected from compounds having insecticidal, acaricidal or nematicidal activity, can be used in combination to effectively control a plurality of pests which are difficult to control by including the above single compounds. The present invention has been completed by pests. In other words, the present invention is composed of the following items: _ π π - a pest control agent, which contains one or more selected ones of the substituted amino quinazolinone compounds represented by the general formula (1) and salts thereof. a compound, and a compound having one or more compounds selected from the group consisting of insecticidal activity, acaricidal activity or nematicidal activity as an active ingredient, general formula [I]

318305 200800021 * , in the above formula, R,: — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — — (C2-C6) alkenyl, (6) (C2-C6) alkynyl, (7) (.-(:6)alkylthio, quinone (8) halogenated (CVC6) sulfur-burning, (9) (CVC6) Alkylcarbonyl, (l〇)(C3-C6)cycloalkylcarbonyl, (11XCKC6)alkoxycarbonyl, (12)(CVC6)alkoxycarbonyl(CVC3)alkyl, (1 3)(Ci_C6) Oxy (C1-C3)alkyl, (14) phenylcarbonyl, φ (15) having a halogen atom, a nitro group, a cyano group, a (CVC6) alkyl group, an s (CVC6) alkyl group, (Cl- C6) a phenylcarbonyl group having an alkyl group selected from the group consisting of an alkoxy group, a halogen (C) rc6) alkoxy group, a (Cl_C6) alkylthio group and a halogen (CrC: 6) alkylthio group (having a plurality of substituents) a substituent, which may be the same or different, (16) phenyl (C2-C6) alkenyl, (17) having a self-clearing atom, a nitro group, a cyano group, (Ci_C6) on its ring Burning base, functional (Cl-C6) alkyl group, (Ci_C6) alkoxy group, functional (C1_C6) alkoxy group, (CVQ) sulfur-burning group, halogen (Ci_c6) sulfur-burning group and (CVC2) stretching base dioxygen Base 318305 7 200 800021 Select phenyl group based on 5 substituents (C! You 6) 1 (with multiple substitutions -3⁄4, the substituents may be the same or different) 1 (18) Phenyl (c2_C6) alkynyl Or (19) has a halogen atom, a nitro group, a cyano group, a (C^CO alkyl group, a halogen (Κ6) alkyl group, a (C "C6) alkoxy group, a halogen (CVC6) alkoxy group) , (Ci-C6) thiol group, halogen (Ci-Ce) thiol group and (C^-C^) decyl dioxy group selected from 1 to 5 substituents of phenyl (C2-C4) alkyne a group (when having a plurality of substituents, the substituents may be the same or different), R1 represents a pyridyl group or a pyridine-N-oxide group, and Z represents _N=C(R2)_ (wherein R2 represents a hydrogen atom (CVC6)alkyl or halo(CirC6)alkyl) or n(r3)-ch (in the formula r2H, r2 represents a hydrogen atom, (cr_c6)alkyl or _(c^-q) alkyl, and R3 represents hydrogen Atom or (CrQ), X shows: (1) bromine atom, (2) iodine atom, (3) hydroxyl group, (4) (CVC6) alkyl group, (5) (C2-C6) alkenyl group, (6) (CVC6) alkynyl, (7) sec (CVC8) alkyl, (8) ((^/6) alkoxy, (9) halogen (CVC6) alkoxy, (10) halogen (Ci-C6) Alkylthio, (11) halogen (Ci-C6) pyridene, (12) halogen ( CVQ) Alkylsulfonyl, 318305 8 200800021 ... Γ13) Halogen (CfCJ oxooxy halogenated XCi-CJ alkoxy" _-(14) carboxy, (15) ((^^6) alkoxycarbonyl' ( 16) an aminocarbonyl group, (17) a substituted aminocarbonyl group having 1 to 2 substituents selected from (Q-C6)alkyl, (C2-C6)alkenyl and (C2_C6)alkynyl groups (having plural In the case of a substituent, the substituent may be the same or different), (18) phenyl, 10 (19) having a halogen atom, a nitro group, a cyano group, a (CVC6) alkyl group, a halogen (Ci_C6) alkyl group, (Ci -C6) a substituted phenyl group having a substituent of 1 to 5 substituents selected from an alkoxy group, a halogen (Ci.Cg) alkoxy group, a (Ci_C6) alkylthio group and a halogen (CrC6) alkylthio group (having a plurality of substituents) Wherein, the substituent may be of the same or different structure), (20) phenyl (Ci-C3) alkyl, (21) having a halogen atom, a stone succinyl group, a cyano group, (c^cj rualkyl group) on its soil. a substituted benzene having 1 to 5 substituents selected from the group consisting of a halogen (CVQ) alkyl group, a (CVCd alkoxy group, a halogen (CVC6) alkoxy group, a (G-C6) thiol group, and a halogen (CrC6) sulphur group. a base (CkC3) alkyl group (having a plurality of substituents, the substituent may be a phase Or different), (22) phenyloxy, or (23) having a halogen atom, a nitro group, a cyano group, a (Ci_C6) alkyl group, a dentate (CVC6) alkyl group, a (CrC6) alkoxy group, and a (Ci_c6) group. a substituted phenyloxy group selected from the group consisting of an oxy group, a (Ci_c6) alkylthio group and a halogen (Ci-C: 6) alkylthio group to 5 substituents (having a plurality of substituents, the substituent may be For the same or not 318305 9 200800021 w 13⁄4 ) ' η shows the number of signatures 1 to 4}; ------------ — — — — — [2] The pests of [1] above a controlling agent, wherein R represents a hydrogen atom, an acyl group, a (c2-c6)alkenyl group, a (cvc6)alkynyl group, a (Cl-c6)alkyl group, a (CkC6) alkoxy group, or (CKC6) Alkoxy (CVC3) alkylcarbonyl, -Z-R1 shows -NH-CHyR1 or -N^CH-Rk wherein R1 represents pyridyl or acridine oxide), X is not a bromine atom, an iodine atom or a halogen (Cr_C8)alkyl, (cvc6)alkoxy, halo(eve:6)alkoxy,halo(Cl_C6)alkylthio,halo(Ci_c6)alkoxyhalo10(Ci_C6)alkoxy, or (c ^c: 6) an alkoxycarbonyl group, an integer of 1 to 2; [3] The pest control agent of the above [1], wherein r is a (Ci_c6) alkyl group a group, -Z-R1 *_NH-CH2_ri (wherein R1 represents a pyridyl group), and a halogen (Ci_C8) alkyl group η is an integer of 1; [4] the pest control agent of the above [1], wherein The substituted amino-based quinone ketone compound or a salt thereof is acetyl group _3,4_dihydro_3_[(3_σ ratio methyl group) -6][1,2,2,2 -tetrafluoro-1-(trifluoromethyl)ethyl]-2(111)啥 嘛 酮 • 或其 或其 或其 或其 或其 或其 或其 或其 或其 或其 或其 η η η η η η η η η η η η η η η η η η η η η η η Acaricidal or nematicidal activity compounds are acetylcholinesterase inhibitors, acetylcholine receptor inhibitors, GABA-regulated chloride channel agonists, sodium channel modulators, nicotine acetylcholine receptors Agonists, acetylcholine receptor agonists, chloride channel activators, juvenile hormones (juvenilehQi>mQn0 mimics, oxidative phosphorylation inhibitors and ATP formation inhibitors, oxidative properties caused by chloride ion gradient disturbance Acid-filled uncoupling agent, for the homopterin synthesis inhibitor (丨 type), quercetin agonist / peeling inhibitor, Zhang Bei 318305 10 200800021 ... guanamine promotes 1 dose, 1 set Electricity Delivery line obstruction (ME TI agent) "position Π - electron transport system inhibitor, lipid biosynthesis inhibitor, ryanodine receptor modulator or compound with non-specific mechanism of action (selective food barrier); [6] The pest control agent according to the above [1], wherein the compound having insecticidal activity, acaricidal activity or nematicidal activity is a METI agent, an insecticide, an acaricide, a thiazide IGR insecticide, and a pyrolysis agent. Pyrethroid insecticide, sodium channel blocking insecticide, amine phthalic acid insecticide, organophosphorus insecticide, calcium channel activating insecticide, benzamidine phenyl urea [7] The pest control agent according to the above [1], wherein the compound having insecticidal activity, insecticidal activity or nematicidal activity is acetamiprid, Imidacloprid, nitenpyram, thiamethoxam, cl〇thianidin, dinofuran

(dinotefuran), thiacloprid, flonicamid, carbaryl, BPMC, fenobucarb, miPC; isoprocarb, ethiofencarb, Bigac (卩11111^〇31*1)), euthium (〇乂&111)^1), benfuracarb, methocarb, mecarbam, sulfur Thiodicarb, aldicarb, alanycarb, metolcarb, xylycarb, propoxur, carbofuran, butyl plus (carbosulfan), furathiocarb, endosulfan, aldoxycarb, nanet (11^1;11〇11^1), cyhalothrine, Permethrin, 赛灭宁11 318305 200800021 -(c^permetHrin), silafluofen, cyfiuthrin, beta-cyfluthrin, and tyranoline Traiomethrin), pyrethrin, aiiethrin, acrinathrin, praliethrin, heterologous Esmethrin, tefluthrin, fenpropathrin, alpha_cypermethrin, lambda-cyhalothrin, deltamethrin, fenva- Lerate), esfenvalerate, flucythrinate, fluvalinate, cycloprothrin, ethofenprox, avermectin

(avermectin), milbemectin, emamectin, spinosad, fenitrothion, malathion, methidathion, fenthion, ali Diazinon, oxydeprofos, vamidothion, pirimiphos-methyl, chlorpyriphos, terbufos, ethoprophos, bis-spec pine Cadusafos), fenamiphos, fensulfothion, DSP, dichlofenthion, fosthiazate, isamidofos, fosthietan, Isazofos, azinphos-methyl, disulfotion, oxydemeton-methyl, parathions, tebupirimfos, Ethion, trichlorfon, metamidophos, II 12 318305 200800021 ...Clison XdichBrvosX, nrevlnplios, sulphate-monocrotophos, amazepine (dimethoate), destroy (fo Rmetanate), formothion, naled, methylparathion, cyanophos, diamidafos, propaphos, methyl propane sulphide Sulprofos, prothiofos, profenofos, isofenphos, temephos, phenthoate, sanjun sulfur (<1丨11 ^1;1171¥丨叩]1〇3), Chlorpheniramine scales (〇111〇1£6¥丨叩1108), tetrachlorvinphos, phoxim, isoxathion , pyraclofos, chlorpyrifos-methyl, pyridafenthion, phasalone, phasmet, dioxabenzofos, quinalphos, methyl sulphide Pine (11^5111[61^〇5), acephate, cartap, thiocyclam, bensultap, thiosultap, fenpyroximate Φpyridaben, σ than tebufenpyrad, tolfenpyrad, fenazaquin, dysentery (Pyrimidifen), rotenone (Rotenone), Emilion (117 (at 11 ^ 1:! 1171 | 1〇11), ethylene unitary Queensland (acequinocyl), vinegar nozzle scroll (] [111 &. 7卩}^111), fluridamide (1!11 & 2111 & 111), flubendiamide, fipronil, acetoprole, ethiprole,螨 螨 (卩1*〇卩&巧^6), indoxacarb, metaflumizone, quinomethionate, diafenthiuron, seyheike Cyhextin hydroxide, fenbutatin oxide, Sanya snail 13 318305 200800021

CamitrazT, spiroiirclofen:, piromesifen, spir〇tetramat, chlorfenapyr, binapacryl, chlorobenzene (chlorbenzilate), phenisobromolate, TPIC, nicotine-sulfate, polynactins complex, azadirachtin, hydroxyprOpyl starch, morron Morantel tartrate, sodium oleate, potassium oleate, pyridalyl, teflubenzuron, kefulong

(chlorfluazuron), diflubenzuron, hexaflumuron, novaluron, lufenuron, fluenoxuron, tebufenozide, oxime Methoxyfenozide, chromafenozide, halofenozide, diofenolan, buprofezin, cyromazine, methoprene, eneph Hydroprene, pyriproxyfen, fenoxycarb, pymetrozine, clofentezine, hexythiazox, fenothiocarb, Etoxazole, bifenazate, kelthane; dicofol, benzoximate, tetradifon, dazomet, phosphocarb, Lemamisol HC1, albendazole, oxibendazole, fenbendazole, oxfendazole, metam-sodium ), Triazamate or Bacillus thur Ingiensis ; BT); 14 318305 200800021 , [8] Wang: [1] harmful pesticides, wherein the compound having insecticidal activity, acaricidal activity or nematicidal activity is fenpyroximate, Fenobucarb (BPMC), isoprocarb (MIPC), tebufenpyrad, tolfenpyrad, buprofezin, metaflumizone, Tebufenozide, chlorfenapyr, fluvalinate, teflubenzuron or flubendiamide; 10[9] above [1] to [8] A pest control agent according to any one of the preceding claims, wherein the substituted aminoquinazolinone compound is 1-ethylindolyl-3,4-dihydro-3-[(3-pyridinyl)amino] 6_[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-2(1Η)-quinaldine, a compound having insecticidal activity, acaricidal activity or nematicidal activity a buprofezin, a metaflumizone or a flubendiamide; [10] the pest control agent according to any one of the above [1] to [9], wherein Phase 0 For 1 part by weight of the substituted aminoguanylidene compound, one or more compounds are selected from the compounds having insecticidal activity, acaricidal activity or nematicidal activity in a ratio of 0.01 to 2000% by weight. [11] A method for using a pest control agent for protecting a useful plant from a pest, and treating the object with an effective amount of the pest control agent according to any one of the above [1] to [1〇] a pest, a useful plant of a subject, a seed of a useful plant of a subject, a soil or a cultivation medium; [12] a method for controlling a pest, for controlling a pest, as shown in the general formula (1) of the above [1] Substituted amine quinazolinone compounds and 15 318305 200800021 ... among which a compound of i-type or more is selected, and one or two kinds of compounds having insecticidal-active acaricidal activity or nematicidal activity are selected. The above-mentioned compound as a pesticidal agent of an active ingredient is treated in an amount of from 0.1 to 1000 g per gram of the active ingredient; [13] is substituted by the general formula (1) described in the above [1]. Amine The use of one or more compounds selected from the group consisting of a sulfinone compound and a salt thereof for producing a substituted amino quinazolinone compound represented by the general formula (1) described in the above [1], and a salt thereof Selecting one or more compounds, and a pest control agent for selecting one or more compounds from compounds having insecticidal activity, acaricidal activity or nematicidal activity; and Π4]-species for controlling pests The pesticidal agent to be packaged is contained in an insecticidal activity per 1 part by weight of the substituted aminoquinazolinone compound or a salt thereof, which is represented by the general formula (1) described in the above [1]. One or two of the compounds having acaricidal activity or nematicidal activity are used in a ratio of from 0. 01 to 2000 parts by weight of the compound of φ, and the general formula (I) described in the above [1] One or more selected from the group consisting of a substituted amino group sulfonate compound and a salt thereof, and one or more compounds selected from compounds having insecticidal activity, bactericidal activity or nematicidal activity, Everything is 〇·1 L〇〇〇g proportion of, and to be packaged. (Effect of the Invention) A compound containing one or more selected from the group consisting of substituted amino quinazolinone compounds represented by the general formula (I) and salts thereof, and having insecticidal activity of 16 318305 200800021 - or a pest control agent (hereinafter, abbreviated as "the present, a pest control agent") which selects one or two kinds of compounds of the Han Chinese as a active ingredient in the compound of nematicidal activity I, which cannot be obtained in each single agent. The full-effect medicine can also exert significant effects, and the pests that cannot be prevented by a single dose and the harmful organisms that exhibit resistance, etc., have significant prevention (4). Therefore, the production efficiency of the crop layer is contribution. [Embodiment] In the substituted amino quinazolinone-containing compound or a salt thereof represented by the general formula (1) of the present invention, in the definition of each substituent, "halogen atom" means gas atom and desert. Atom 1 atom or a fluorine atom. Examples of "(4) base" are 2+ base, > 唆 base, 44 唆, etc. "„Materials·oxides” complements 2 “Bit-N-oxide, 3_pyridine_N_oxide, 4•pyridine-oxide, etc. Also, “(Ci-Cy alkyl” is carbon a linear or branched chain of 1 to 12, such as methyl, ethyl, n-propyl, isopropyl, i-butyl, isobutyl, t-butyl, tert-butyl , n-pentyl, isopentyl, # 2 methyl butyl, neopentyl, ethyl propyl, n-hexyl, isohexyl, 'methylpentyl, 3 ·methylpentyl, 2 -methylpentyl , 1-methylpentyl, 3,3-dimethylbutyl, 2,2-dimethylbutyl, u-dimethylbutyl, ! 2-dimethylbutyl, dimethylbutyl, 2,3_Dimethylbutyl, ^ethylbutyl, 2-ethylbutyl, n-heptyl, n-octyl, n-decyl, n-decyl, n-undecyl, n-dodecyl Etc. (But in the abbreviation, "n_" is positive, "i·" is different, "s-" is second, and "t_" is third, the following are the same.) Eight "(c]_c8)alkyl" a linear or branched alkyl group having a carbon number of from 8 to 8, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, 318305 17 200800021—isobutyl, second benzyl, tert-butyl-, n-decyl, iso-pentyl, L-tolyl butyl, neopentyl, 1-ethylpropyl, n-hexyl, isohexyl ,methylpentyl, 3-methylpentyl, 2-methylpentyl, methylpentyl, 3-dimethylbutyl, 2,2-dimethylbutyl, ι,ΐ-dimethylbutyl Base, it dimethylbutyl, 1,3-dimethylbutyl, 2,3-didecylbutyl, ethyl ethyl butyl, decyl ethyl butyl, n-heptyl, n-octyl and the like. "(Ci-C6)alkyl" is a straight or branched alkyl group having from 1 to 6 carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, ♦ Isobutyl, t-butyl, tert-butyl, n-pentyl, isopentyl, 2-methylbutyl, neopentyl, 1-ethylpropyl, n-hexyl, isohexyl, 4-methyl Pentyl, 3-mercaptopentyl, 2-decylpentyl, L-decyldecyl, 3,3-didecylbutyl, 2,2-didecylbutyl, U-dimethylbutyl , u-dimethylbutyl, 1,3-dimethylbutyl, 2,3-dimethylbutyl, j-ethylbutyl, 2-ethylbutyl "(CkCO alkyl) is a carbon atom a linear or branch of the number i to 3 An alkyl group such as a methyl group, an ethyl group, a n-propyl group, an isopropyl group or the like. "(CVC2) a dialkyloxy group" is a methylene dioxydioxy group or the like. The "C6) cycloalkyl group is exemplified by an alkyl group having 3 to 6 carbon atoms in the form of a cyclopropyl group, a cyclobutyl group or a cyclopentahexyl group. ^-〇6) alkoxy group is shown above. (c^) methoxy group in the alkyl group, specifically, for example, methoxy, ethoxy, propoxy=yl, butylene, isobutoxy, tert-butoxy, pentyloxy" 318305 18 200800021 - "(C2_C6)Alkenyl" is a carbon which has a double bond and has a linear or branched alkenyl group of 2 to k, such as an ethyl group or a propylene group. Base, isopropenyl, 1-butenyl, 2-butane, 7 tian _ ^ 丞 肺 lung methacryl, pentenyl, pentadienyl, hexenyl or hexadienyl Wait. (2丄6) alkynyl) is a straight or branched alkynyl group having at least a carbon atom of 2 - 6 or a branched chain, such as an ethynyl group, a 2-propyl group, a pentyl group Alkynyl, pentadiynyl, hexyl or hexadiynyl, and the like. "Chalogen (CkC8) base" means that the number of carbon atoms in the same or different one or more atoms is "linear" or "chain" in the order of 8 to a linear or branched chain. Ethyl, heptafluoropropyl, "2,2,2·tetrafluoro-H; gaseous earth" ethyl, 2,2,2-trifluoro (trifluoromethyl)ethyl, etc. "halogen (CVC6) "hospital base" means a linear or branched singular group of 1 to 6 carbon atoms substituted with the same or different y or more productions, such as Sandon methyl, pentafluoroethyl, heptafluoro The propyl group and the coffee bean are all evaluated as methyl, ethyl, 2,2,2-tris(trimethyl)ethyl and the like. Also, 'halogen (: decyloxy), "halogen (C2_C6) alkenyl" or "halogen". 2 heart: id" 7 is more than one of the above-mentioned halogen atoms substituted by linear or branched The number of carbonaceous materials is from 〗 〖 to 6 oxyl groups = dilute groups or fast radicals having 2 to 6 carbon atoms. When substituted with 2 dioxin atoms, the ruthenium atoms may be the same or different. :) On the second, the base to which the base is attached, for example, "(cvc subsoil i 6), meta-soil" is based on (Ci_C6) alkyl as the main 1 "substitution of substitution (Ci_c6) alkoxy can be The same or 318305 19 200800021 is different. Further, the salt of the substituted aminoquinazolinone compound represented by the general formula (I), for example, a salt with an inorganic acid such as hydrochloric acid, sulfuric acid, nitric acid or phosphoric acid, can be exemplified with sodium. An alkali metal salt such as potassium, an alkaline earth metal salt such as calcium or magnesium, or the like, and the substituted amino quinazolinone compound may be a salt of a transition metal such as copper, rhodium or iron or a complex thereof. The substituted aminoquinazolinone compound represented by the general formula (I) of the present invention or a salt thereof has two kinds of geometry derived from a carbon-nitrogen double bond in its structural formula The present invention includes all of the respective geometric isomers and a mixture thereof in any ratio. Among the substituted aminoquinazolinone compounds represented by the above (I) or a salt thereof, R is preferably a halogen atom. (Cl_Cl2)alkyl, (C2_C6)alkenyl, (C2-C6) fast radical, (CVC6) alkyl radical, (CVC6) alkoxy group, or (Ci_c6) alkoxy (CVC3) alkylcarbonyl , -Z-R1 is -NH-CH2-R1, or wherein R is pyridyl or pyridine-N-oxide, X is a 10 bromine atom, an iodine atom, a halogen (Cl-c8) alkyl group, Ci_C6) alkoxy, halo(Ci_C6)alkoxy, dentate (cvc6)alkylthio, halo(Cl_C6)alkoxy (i), or (CrC6) alkoxycarbonyl, n is 1 An integer of 2, more preferably i. More preferably, for example, R system (CVC6) entertainment: benzyl group, -Z-R1 system -NH-CH-R1 (wherein R represents 吼σ疋 group), X system halogen (c _c8) a base, η system 1. The above pyridyl group or pyridine-N-oxide group represented by r1 is more preferably a 3-pyridyl group or a rhodium-platinum oxide group. The first one used in the present invention The substituted amino quinazolinone compound represented by the general formula (1) of the active ingredient can be used in accordance with Japan. It is produced by the method described in the Japanese Patent Laid-Open Publication No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. No. Hei. -pyridylmethyl)amino]-6-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-2(111)-quinazolinone (1-acetyl-3) , 4-dihydr0-3-[(3-pyridylmethyl)amino]-6-[l?25252-tetrafluoro-l-(trifluoromethyl)ethyl]-2(lH)-quinaz olinone (in the following Table 1, Νο· The compound of 15, hereinafter abbreviated as the compound (a), or the one shown in the table (a)) can be produced by the method described in Japanese Patent Laid-Open Publication No. 2001-342186 or the like. In the first or second table, a typical compound is exemplified, and the present invention is not limited to the above-mentioned range, and a compound disclosed in Japanese Laid-Open Patent Publication No. Hei 8-325239 and JP-A No. 2001-342186 can be exemplified. The compound represented by the general formula (I) includes a compound represented by the general formula (I-1) and a compound represented by the general formula (1-2). General formula (1-1): 21 318305 200800021

3/NH—CH2R1 Ή 8 N^IUDn

(Ι-D No. 1 No. R R1 In Physical property 1 HQ! 6-CFs Bp. 191.0-193· It: 2 & Ql 6HBr Bp· >300*0 3 H a1 6-C2Fs p. ISS-HSt : 4 H Q1 6-CF(CF山1P.1S9.4-I6K01C 5 H Q1 en-CgFjj mp.I53.9-lM.7lC 6 H Ql 6-0CF, nD 1.5233(22· fit:) 7 H Q1 6-OCHF, up. 129.7-130.2^ 8 H Q1 6-SC, F7-i p. 50.3-53· 11C 9 H Q1 6-OCFiCHF, mp.I68.7-173.9 10 H Ql e-CFCCFi), House p· 239· 7-243· 5 11 COCH, Q1 6-0CF, nD 1.5478 (24. 11C) 12 C0C2H5 Q1 6-0CF, nD 1· 5174 (25· 90 13 CH.CsCH Q1 6-0CF, dD 1.5325 (24.21C) 14 COCH, Ql 6-0CHF2 nD 1.5503 (26.110) 15 COCH3 Ql 6-CF(CF,)t BP.132-134TC 16 COOKCH,), Q1 fi-CFCCF,), nD 1.5051 (22·It :) 17 C0C2H5 Qr 6-CF(CFs), p. 10S1C 18 COC3H7-11 Q1 6-CF(CF3)2 nD 1.510(22.2*0 19 H Q1 6-C00C2Hs ρ·168· 7-171.9*0 20 C0C , Hs Q1 6-CF3 nD K5400 (21·11C) 21 COOCH3 Q1 6-CF(CF3)2 P.I30-135X: 22 COOCA Ql 6-CF(CFs)2 23 C00C4H,-1 Ql 6-CF(CF Mountain & D 1.5598 (23.4t:) 24 COCHjOCH, Q1 6-CF (CF3h nD 1.5106 (21. St:> General formula (1-2): 22 318305 200800021

(1-2)

No· R R1 Xn ~ Physical property 25 Η Ql TTt 26 Η Ql 6, C, FS p.298-30〇r 27 Η Q1 6-CF(CFJ, p.>300t: 28 Η Q1 δ-n-CtFii p .>300t: 29 Η Q, TocFT Βφ· 264· (H266· (TC 30 Η Q1 Tochf, - ap· 260.1-264.St: 31 Η ar 6*~SCjF^-i ap· 252·4-255 ITC 32 ch,ch:ch2 Ql 6·Ι P.162-1641C 33 Η Ql J - 0CF,CHFt p. 251.6-263.31C 34 C0C,H5-c Q1 6_I p. 172-1761C 35 Η Q1 lF〇CH (CF,). ^ \φ·>300Χ: 36 Η Q1 〇CFtCHF0CFs p. 240.2-241.3X: 37 COOCHs Q1 Bu CF (CF Hill P.160H65X: 38 C0CHa Q1 p.186-188T: 39 C0C, Hs Q1 6-f P.135-1391C 40 CiHs Q1 6-1 ΒΡ·19Ι.5·194·δΤ: Also, the symbols in Tables 1 and 2 have the following meanings: η shows positive, i shows difference' t indicates that the third 'c represents an alicyclic hydrocarbon group (for example, C3H5-C shows a cyclopropyl group), Ph represents a phenyl group, Q1 represents a 3-pyridyl group, and Q2 represents a 3-pyridine-N-oxide group. A compound having acaricidal activity or nematicidal activity, for example, an acetylcholinesterase inhibitor (for example, an aminoformate compound, an organophosphorus compound) or an acetylcholine Alkaline receptor inhibitors (such as cartap, etc.), GABA-regulated chloride channel agonists, sodium channel regulation (such as sputum removal of veterinary vinegar compounds), nicotine acetylcholine receptors 318305 23 200800021 Pharmacological agents (such as the final check chlorine compound), acetylcholine receptors and health effects (example & spinosyn), chloride channel activator, health care Agent, oxidative phosphorylation inhibitor and ATP formation inhibitor (for example, organotin compound), oxidative acidification of sedative stomach sputum caused by hydrogen ion gradient disturbance (for example, chlorfenapyr), for Homoptera Chitin-synthesis and anti-inducing agents (type 1) (such as buprofezin), ecdysone agonist / de- amp; inhibitors (such as diacylhydrazine), octopus Wen Qiao (such as amitraz), position I electron transport system inhibitor (such as METI agent), position II electron transport system inhibitor, lipid biosynthesis blocker (for example, river J acid compound), blue Nitidine receptor modulators (eg, flubendiamid) e)), or a compound that has a non-specific mechanism of action (selective inhibition) (e.g., Flonicamid). Among them, people with insecticidal activity, acaricidal activity or nematicidal activity are METI-based insecticides, acaricides, thiazoline IGR-based insecticides, and: 4. Pyrethroid-based insecticides, Sodium channel blocking insecticide, amide formic acid insecticide, organophosphorus insecticide, insecticidal agent with calcium channel activation _ phenyl phenyl ureido insecticide, diterpene lanthanide Insecticides and the like are preferred. The above specific examples are exemplified by the following specific names, and the present invention is not limited to the scope. For example, compounds having insecticidal activity, acaricidal activity or nematicidal activity are acetamiprid, imidacloprid, nitenpyram, thiamethoxam, and clothianidin. , chloramphenicol compounds such as dinotefuran, thiacloprid, flonicamid, etc., Kabali 24 318305 200800021 • carbaryl, 免 gram (611〇511 ( ^作;61>]\4(:); extinction - (isoprocarb; MIPC), ethiofencarb, pyrimicarb, oxamyl, benfuracarb, Methicarb, mecarbam, thiodicarb, aldicarb, alanycarb, metolcarb, xylycarb, Andan Propoxur), fenothiocarb, carbofuran, carbosulfan, furathiocarb, endosulfan, aldoxycarb, nanet Aminomethane compound such as methodoy, cyhalothrin (cyhalothrine), permethrin, cypermethrin, bifenthrin, halfenprox, silafluofen, cyfluthrin, beta vasine Beta_cyfluthrin), tramomethrin, pyrethrins, allethrin, acrinathrin, prallethrin, remethrin , tefluthrin, fenpropathrin, alpha-cypermethrin, lambda-cyhalothrin, delta_methrin, fenvalerate, fennelly (esfenvalerate), flucythrinate, fluvalinate, cycloprothrin, ethofenprox, pyrethroid compounds, avermectin, A compound that activates chloride channels such as emamectin-benzoate and milbemectin, and sputum receptors such as spinosad. 25 318305 200800021 Ester compound (fenitrothion), malathion, methidathion, fenthion, diazinon, oxydeprofos, vamidothion, pirimiphos -methyl), chlorpyriphos, terbufos, ethoprophos, cadusafos, fenamiphos, fensulfothion, DSP, deichlofenthion , fosthiazate, isamidofos, fosthictan, isazofos, thionazin, azinphos-methyl, disulfide Disulfoton, oxidemeton-methyl, parathions, tebupirimphos, ethion, trichlorfon (DEP), 曱Meimidophos, diclofen ((11〇111〇1^〇5; 00\^), mevinphos, monocrotophos, dimethoate, formetanate , formothion, thiometon, naled (BRP), methyl Methylparathion, cyanophos, diamidafos, propaphos, sulprofos, prothiofos, profenofos, alfene Isofenphos, temephos, phenthoate, dimethylvinphos, chlorferinphos, tetrachlorvinphos, phoxim, plus Fukusong (isoxan1; hin), pyraclofos, chlorpyrifos-methyl, pyridafenthion, feisailong 26 318305 200800021 • (pHosaIone) T phosmet, killer 嵩cdi〇xal )enz^p〇s), quinalphos, mesulfenfos, acephate and other organophosphorus compounds, cartap, thiocyclam, free speed ( Bensultap), thiosultap, and other nereistoxin-like compounds, fenpyroximate, pyridaben, tebufenpyrad, tolfenpyrad, and fentanyl Fenazaquin), pirimifife n), rotenone (rotenone), Φ, II, electron transport system, hinder compound, fluazinam, etc., oxidative phosphorylation inhibitory compound, flubendiamide A compound having a calcium channel activating action such as a fipronil, an acetoprole, or an ethiprole, etc., such as a compound of Νο·124 described in JP-A-2001-131141. GABA regulates the activity of chloride channel agonist phenylazole compounds, sulfite compounds such as propargite, indoxacarb, metflumizone, etc. A sodium channel blocking system compound such as a compound described in Japanese Patent Publication No. 5-17428, a quinomethionate, a phthalate compound, a diafenthiuron, a cyhexatin, and a fen An organotin-based compound such as fenbutatin oxide, which has an inhibitory effect of oxidative phosphorylation, a compound which inhibits ATP formation, and a steroidal compound having an octopus extended amine agonist such as amitraz A spirulina compound, such as spirodiclofen, spiromesifen, and spirotetramat, which has a lipid-synthesis-inhibiting effect, chlorfenapyr 27 318305 200800021 • (cHorfenapyr), Baikeke (13111 and &. 71) Qin-oxidation is an acidified uncoupling agent of nitrophenyl crotonic acid compound, chlorbenzilate, phenisobromolate, isocyanuric acid tripropyl S (TPIC; tripropylisocyanurate And other anti-ant compounds, such as nicotine-sulfate, polynactins, azadirachtin, hydroxy propyl starch, morantel tartaric acid A fatty acid alkali metal salt compound such as a natural substance such as a salt, a sodium oleate or a potassium oleate, and a pyridalyl such as a protein synthesis inhibitor, an insect growth regulating substance (IGR) Compounds such as tefiubenzuron, chlorfluazuron, diflubenzuron, hexaflumuron, novaluron, lufenuron, flubendiles Flubenoxuron and other benzamidine phenylurea compounds having a hindrance to chitin synthesis, tebufenozide, methoxyfenozide, chromafenozide, halfino (ha) Lofenozide), such as a dimercapto steroid compound having a ecdysone agonist, a peeling inhibitor such as diofenolan, and a diterpenoid compound having a homotropanic peeling hindrance such as buprofezin , cyromazine (cyromazine) and other diptera peeling hindering compounds 'methoprene, methionine (117 (11 * 〇卩 16116), pyriproxyfen, fenoxycarb (fenoxycarb), etc. Juvenile hormone-like compounds, pymetrozine, clofentezine, hexythiazox, fenothiocarb, etoxazole, bifenazate, large Dicofol, Cet. 28 318305 200800021 * ^{benzoximate) - ^ (tetradifon) # ^ t Compound i Others such as dazomat, phosphocarb, etc., levamisole hydrochloride ( Levamisol HC1), albendazole, oxibendazole, fenbendazole, oxfendazol, etc., methyl for metam-sodium a dithiol phthalate compound, Triazamate, or Bacillus thuringiensis (BT) agent. Among them, fenpyroximate, fenobucarb (-_BPMC), isoprocarb (MIPC), tebufenpyrad, tolfenpyrad, buprofezin ), metaflumizone, tebufenozide, chlorfenapyr, fluvalinate, tifuton (^£11^6112111*〇11) or fluorobenzene Flubendiamide is preferred. Also known as fenpyroximate, tebufenpyrad, tolfenpyrad, buprofezin, metaflumizone, tebufenozide, bromo More preferably, chlorfenapyr, fluvalinate, teflubenzuron or flubendiamide. Especially buprofezin, metalfumizone or flubendiamide is preferred. Typical examples of the pest control agent of the present invention are, for example, 1-ethylindolyl-3,4-dihydro-3-[(3-acridinylmethyl)amino]-6_[U2,2,2-tetrafluoro 1-(Trifluoromethyl)ethyl]-2(1H)-quinazolinone or a salt thereof, and buprofezin, metalfumizone or fluorobenzamide 29 318305 200800021 .(frubendiamrde)—“Best—when using the pest control agent of the present invention for a bupro-fezin-containing system, the composition 1 is used as an active ingredient compound The amount to be added is preferably selected from the range of from 0.1 part by weight to 50 parts by weight, preferably from i to parts by weight. Further, the substituted amino quinazolinone compound (1) in the active ingredient compound is selected from the compounds having insecticidal activity, acaricidal activity or nematicidal activity, and the ratio of the addition of the compound or the two or more compounds 'Compared to 1 part by weight of the substituted aminoquinazolinone compound (1), • one or more compounds selected from compounds having insecticidal activity, bactericidal activity or nematicidal activity are preferred A moderate range is preferably selected from the range of 1 to 2 parts by weight, and it is preferably selected from the range of from 1 part by weight to 1 part by weight. The pest control agent of the present invention can be prepared into a suitable solid, liquid or powder form according to the general method of the pesticide preparation, and if necessary, the carrier can be formulated in an appropriate proportion by using a proper ratio of the carrier and the like. Additives such as agents, sclerosing agents, surfactants, solid fluidity improvers, suspending agents, peptizers, antifoaming agents, preservatives, spreading agents, decomposing agents, ultraviolet light absorbers, etc., are melted and pulverized , suspension, mixing, impregnation, adsorption or adhesion, according to the purpose of use to prepare appropriate dosage forms, such as emulsions, milk suspensions, powders, granules, granule hydrating agents, hydrating agents, suspending agents, flowable agents, It is used as a liquid agent, a large amount of packaging agent, or a spray. The pest control agent of the present invention is suitable for pest control of various agricultural and forest pests, horticultural pests, storage pests or sanitary pests or nematodes such as rice, vegetables, fruit trees, chemical plants, etc., for example, Hemiptera (Hemcaa) ) 318305 30 200800021 • Heteroptera (Megacopta punctatissimum), Eysarcoris lewisi, Eysarcoris parvus, Nezara viridula, Plautia stali, Cletus punctigen, Leptocorisa chinensis, Riptortus clavatus, Togo hemipterus, Pear crown net ( Stephanitis nashi), Stephanitis pyrioides, Apolygus spinolai, Stenotus rubrovittalus, Trigonotylus coelestialium, etc., such as the homoptera (Homoptera) Arboridia apicalis, Empoasca onukii, Nephotettix cincticeps, black tail Nephotettix virescens, Laodelphax striatellus, Nilaparvata lugens, Sogatella furcifera, Diaphorina citri, Aleurocanthus spiniferus ), Bemisia argentifolii, Bemisia tabaci, Dialeurodes citri, Trialeurodes vaporariorum, Viteus vitifolii, Eriosoma lanigerum , Aphis citricola, Aphia craccivora, Aphis gossypii, Aulacorthum solani, Brevicoryne brassicae, Macrosiphum euphorbiae, nectarine Myzus persicae, Rhopalosiphum padi, Sitobion akebiae, Pseudococcus 31 318305 200800021 'comsiocki, Ceroplastes ceriferus, Fuhong only Aonidiella aurantii, Comstockaspis perniciosa, mulberry Insect shell (Pseudaulacaspispentagoa), arrow worms dielectric housing (Unaspisyanonensis) and the like. For example, Adoxophyes orana fasciate, Adoxophyes honmai, Archips fuscocupreanus, Caposina niponensis, and Grapholita 10molesta in Lepidoptera ), Homonamagnanima, Caloptilia theivora, Ascotis selenaria, Endopiza viteana, Laspeyresia pomonella, Phyllonycter ringoniella , Lyonetia pnmifoliella malinella, Phyllocnistis citrella, Plutella xylostella, Pectinophora gossypiella, Carposina niponensis, Chilo Suppressalis), Sanhua Momo# (Scirpophagaincertulas), Cnaphalocrocis medinalis, Hellullaundalis, Papilio xuthus, Pieris rapae crucivora, Yellow caterpillar caterpillar (Malcosoma Neustria testacea), American white moth (Hyph Antria cunea), Parapediasia teterrella, Helicoverpa armigera, Heliothis spp., Agrotis segetum, Autographa nigrisigna, Gan 32 318305 200800021 — Such as 11 〇), Spodoptera litura (8? 〇 (^〇卩{6^111; 1^) and other plants such as Coleoptera, Anomala cuprea, Popillia japonica, Lyctus brunneus, Tribolium confusum, Epilachna vigintiocto punctate, Anoplophora malasiaca, Monochamus alternatus, and green bean (Callosobruchus) Chinensis) ^ $ (Aulacophora femoralis) ^ corn rootworm (Diabrotica spp.), cotton boll weevil (Anthonomus gradis _ grandis), Mexican black bean ladybug (Epilachnavarivestis), Colorado golden flower worm (Leptinotarssa decemlineats), rice water weevil (Lissorhoptrus oryzophilus), Oulema oryzae, Sphenophrus venotus vestitus, etc., such as Hymenoptera (Hym) Enoptera) Athalia rosae ruficornis, Arge pagana, Formica japanica, etc.

For example, in the Diptera (Diptera), the rice larvae (human $1*〇111}^& oryzae), Hydrellia griseola, Liriomyzatrifolii, Delia antiqua, Musca domestica, Culex pipiens molestus, Culex pipiens pallens, etc., such as the small yellow horse (Scirtothrips dorsalis) in the Thysanoptera, the southern yellow horse (Thrips) Palmi), Thrips tabaci, Frankliniella occidentalis, etc., for example, termites in the family Apoptera (Coptotermes 33 318305 200800021 • formosanus), yellow chest loose * ^ (Reticulitermes speratus) Ti (Psocoptera), Liposcelis bostrychophilus, and the like. For example, in the Orthoptera, 小xya yezaensis, Gryllotalpa sp., Pedplaneta Americana, Blattella germanica, etc., for example, in Acarina Panonychus citri, Panonychus ulmi, Tetranychus urticae, Tetranychus kanzawai, Brevipalpus phoenicis, Brassica (Bryobia praetiosa), Aculops pelekassi, 20th century Eriophyes chibaensis, Polyphagotarsonemuslatus, Rhizoglyphus robini, Tyrophagus putrescontiae, etc. For example, the root rot nematode (Pratylenchus coffeae), the pratylenchus penetrans, the Globodera rastochiensis, the Meloidogyne incognita, etc. in the case of Tylenchida, such as pseudo-nematodes (Dorylaimida), such as Longidorus sp., etc., for example, in the soft-skinned gastropod (Gastropoda) Wire began snail (Incilariabilineats) and so on. The useful plant of the object to be used for the pest control agent of the present invention is not particularly limited, and examples thereof include cereals (for example, rice, barley, wheat, rye, oats, corn, etc.), and beans (for example, soybeans, red beans, peas, beans, and beans). Beans, flowers 34 318305 200800021 .1, etc.), fruit trees, fruits - such as apples, citrus-li

Plum, cherry, walnut, fruit, apricot, citrus grape, F cans such as cabbage, sage, bok, green leaf, fruit and vegetable: sub-two, two-two ocean: potato green r such as cotton, hemp, Flame vegetables, hops " blade (1) coffee, tobacco, apple, etc.), 庶, sweet, 撖 、, rubber, sweet; LA pumpkin, courgette, squash, watermelon, melon 4), pasture (for example, garden瓜伊音允曾Μ笠, Zheshan early ψ蜀黍, 提牧卓, 苜 、, 糸化目伯 4), Zhuopi (such as sorghum, thyme, fragrant, 刼^, etc.), flowers (such as chrysanthemum, rose flower, carnation, orchid::: trees (such as ginkgo, cherry blossoms *, garden music, μ Γ peach scales), forest trees (fir, shrimp, pine, pine, cypress, Plants such as cedar, eucalyptus, etc.. 'This useful (4) may include the production of insecticidal active ingredients by genetic recombination, etc. #长过転中. Plants that are placed into a knife. The active ingredients of the insecticide, such as toxins, are controlled. Various pests and diseases, the harmful connection of the present invention, or the appropriate enthalpy of water, such as water, can be used to dilute π in the sheet J τ to be diluted with The form of suspension will prevent pests: the effect is used in addition to the plants that can predict the production of harmful organisms, - the main strong ten pests are scattered in the stems and leaves, the sound is into the medicine = the medicine, using the powder coating Seeds such as peel treatment, planting, planting, planting, soil mixing, seedling box treatment, * eight sputum treatment, soil fertilization, rice seedling box treatment, water surface application, etc. or treatment of soil and other roots In addition, it can also be used in hydroponic cultivation. In the hydroponic cultivation, Shige is used for cultivating ash, fumigation or stalking into the trunk, etc. It can also be distributed in, for example, storage pests, house pests, sanitary pests, and wood worms. In addition to use, it can also be used for painting of home building materials, fumigation de-ashing liquid, etc. ..., methods of treating seeds, for example, m ^ ^ in liquid or solid form, or after dilution The method of infiltrating the seed by liquid, soaking the agent == the agent or the liquid preparation and the seed are mixed, or the powder coating is applied to the body or the like, and the resin or the liquid preparation is used. a method of applying to a seed, Or the method of dispersing the solid preparation or the liquid preparation in the vicinity of the seed, etc. in the back of the seeding. The above-mentioned treatment of the seed described in the above-mentioned plant, for example, the insertion of the plant. In addition to 嫉 method, including various bulbs, tubers, seeds, beads, bulbs or cuttings, etc. ^ When using the method of the invention, the plant "the soil, two #贝Special restrictions, as long as the material that can be grown by the shuttle, can be:, two: =, water, etc., such as sand, stone, stone, frozen, agar, gelatinous material, high-quality "glass cedar, wood chips" , bark, paper, etc.... sub-objects, rock wool, preparations or hydrating agents or granular hydration: 2: the method of ": 1 = dilution method # 襄" after the flowable agent, for example, Liquid preparation diluted with water 318305 36 200800021, pre-dispersed powder, hydrating agent, granules:::: square 2: before or after transplanting. Mixing method, or before planting or before planting; Mixture, granules are equal to planting points, planting =,, = mixture, granule rice seedling box t :: administration of the agent with the administration of transplantation period of administration, etc. while administering: Multicast = two, green agent, granular wettable powder, granules and the like dosage forms can. The sling can be mixed with the culture soil, the θ a , or the granulated water culture soil by mixing with the granules or granules, and the soil can be mixed and coated in a layer form. 5 only the various preparations and culture soil cross-water: medium application method, usually, in the water-like paddy field sergeant: a large amount of packaging agents, granules, granular hydrating agents and other solid preparations, ς == preparations, emulsions, etc. A method of dispersing a preparation or the like. Others can be used to distribute the fertilizers into the water source. The water source or the irrigation device can be used for water supply. Labor saving. The application of dryland crops can be carried out on the seeds or in the cultivation medium close to the plant body during the self-seeding, seedling period and growth period. Direct sowing In plants in dry land, in addition to directly treating the preparation to the seed, it is preferred to treat the base of the plant in the cultivation with the preparation. It may be treated by granule dispersion, or may be treated by liquid infusion with a drug diluted with or without dilution. It is also a good method to mix the granules with the cultivation medium before sowing. The cultivated plants that need to be transplanted are treated in the sowing and seedling stage, 318305 37 200800021. In addition to the direct treatment of the seeds, it is better to disperse the liquid preparation or the granular preparation in the seedling bed for seedlings. In addition, it is also a good method to plant the acupoints at the time of planting, or to mix the cultivation medium adjacent to the transplant site. > The bio-control agent of the present invention is generally manufactured (4), for example, a ritual, a ritual suspension, a hydrating agent, a granular hydrating agent, a suspending agent, a flowable agent, a liquid agent, a granule, A dosage form of a powder, a bulk packaging agent, a misting agent, a fumigant, etc., the amount of the composition, the blending ratio of the financial effect component, the meteorological condition, the form of the preparation, the application period, the application method, the application site, and the control It is different from the target pests, the target crops, etc., and usually, the effective components of the production (including the compound of the general formula (1) and the sum of the compounds of the aphid activity, the bactericidal activity or the nematicidal activity) are exchanged. The application may be appropriately selected from the range of .ig to iooog, and it is preferred to select the application in the range of ig, 500 §. When the seed is treated, and the seed weight is converted to the active ingredient in the rut preparation, it may be used in the range of Μ to %%, among which it is preferably used in the range of 〇1 to 1%. When it is applied by diluting an emulsion, a hydrating agent or the like with water, it is applied at a concentration of 0.00001 to 1·1%, granules, powders or liquid preparations for seed treatment, and the like, and it is usually used without being diluted. χ '% in the present invention, generally means % by weight (w/w) 0. In addition, the period of use of the pest control agent of the present invention, in order to prevent simultaneous diseases and/or weeds, other active ingredients a compound having insecticidal activity, bactericidal activity or nematicidal activity, which can be used simultaneously with a compound having bactericidal activity or herbicidal activity and a compound having insecticidal activity m or nematicidal activity 318305 38 200800021 τ It is expected that the synergistic effect of the herbicide effect can be expected by controlling the range of pests and diseases of the object and reducing the amount of the drug. The compound having bactericidal activity or herbicidal activity, such as the following compounds. Examples of bactericidal active compounds such as azoxystrobin, dilococymet, pyroquilon, kasugamycin, propyl chelsone (^1'〇7 & 1^ 〇5;16?), hymexazol, mepronil, tricyclazole, edifenphos, isoprothiolane, blastcidin , flutolanil, dynasty ((11(;1〇11^211]^), pencycuron, carbendazin, dodine, puffer ( Propamocarb), pyrimethanil, fluquinconazole, focetyl-AL, bromuconazole, triticonazole, fluxetover, imipenem Fenamidone, tolylfluanid, dichlofluanid, trifloxystrobin, triadimenol, spiroxamine, fenhexamid, Iprovalicarb, fthalide, iprodione, thio Phanate), benomyl, triflumizole, fluazinam, zineb, captan, manzeb, fenremore Fenarimol), calcium polysulfide, triadimefon, vinclozolin, dithianon, bitertanol, polycarbamate, gram heat (iminoctadine-DBS), gram grass enemy 39 318305 200800021 • (pebulate), polyoxin-B (polyoxin-B), methyl zinc napro (propineby, chinomethionat, dichlofluanid, tetrachloroiso Chlorothalonil, difenoconazole, fluoroimide, 赛福宁 01^〇1^1^), octopus (uncle & (!1 and 71), streptomycin ( Streptomycin), zinc mannep (111 & 11 (; 〇 2613), oxolinic acid (〇 〇 1111 沁 acid), mepronil, metalaxyl, propiconazole, phenanthrene Hexaconazole, sulfur, pyrifenox, basic copper sulfate, Mouth # (pyrimethanil), iprobenfos, tolclofos-methyl, maneb, thiophanate-methyl, trifluzamide, flor Ratio (furametpyr), flusulfamide, kresoxim_methyl, carpropamid, hydroxyisoxazole, echlomezole, procymidone, gram Vinclozolin, ipoconazole, furconazole, myclobutanil, tetraconazole, tebuconazole, imibenconazole, poker 卩1 ^〇(:111〇^2), pefurazoate, cyproconazole, mepanipyrim, thiadiazin, probenazole, benzoxadiazole Acibenzolar-S-methyl), validamycin-A, fenoxanil, tiadinil and other fungicides can be used in combination. Secondly, compounds with herbicidal activity, such as free radical 40 318305 200800021 ^ (bensulfuron-metliyl), four azlmsulfuron, cinosulfuron, cyclosulfamuron, ° ratio Pyrazosulfuron-ethyl, imazosulfuron, indanofan, cyhalofopbutyl, thenylchlor, esprocarb, acetophenone Amine (etobenzanid), cafestrole, clomepTop, dimethametryn, daimuron, bifenox, pyributicarb, sigma φ (pyriminobac-methyl), pretilachlor, bromobutide, benzofenap, benthiocarb, bentoxazone, benfuresate , mefenacet, ethyl fenoxaprop-P_ethyl, phenmedipham, diclofop-methyl, desmedipham, ethofumesate ), isoproturon,Amidosulfuron, anilofos, benfuresate, ethoxysulfuron, ° iodosufluron, diphenyl sulphur acid (isoxadifen), methamsulfuron, foramsulfuron, double-mouthed grass (卩)^&〇1〇1111), mesosulfuron, diuron, niblon Neburon), dinoterb, carbeamide, bromoxynil, oxyadiazon, dimefuron, diflufenican, dipivoxil Aclonifen), benzofenap, 17 oxaziclomefone, isoxaflutole, oxadiargyl, flurtamone, chlorhexidine 41 318305 200800021 • (metribuzin), methabenzthiazuron, tribufos, metamitron, ethiozin, flufenacet, thioglycone (sulcotrion), fentrazamide, propylidene huanglong (卩1*〇卩〇\}^&1^&2〇1^) On one Danhuang Long (flucarbazone), sulcotrione laugh amine (metosulam), saliva oxadiazon amine (amicarbazone) and other herbicides, for a mixture. Further, the herbicides described in the following general names may also be used in combination. For example, glyphosate-isopropyl amine, glyphosate-trimesium, glufosinate-ammonium, bialaphos, butamifos, Prosulfocarb, asulam, linuron, calcium, peroxide, alachlor, pendimethalin, acifluofen- Sodium), lactofen, ioxynil-octanoate, alloxydim, sethoxydim, napropamide, mouth-to-mouth (pyrazolate), pyraflufen-ethyl, imazapyr, sulfentrazone, oxadiazon, paraquat, diquat ( Diquat), simazine, atrazine, fluthiacet-methyl, quizalofop-ethyl, bentazone, BAS-3510- H, triaziflam (triaziflam) and the like. Further, thidiazuron, mefenpyr, ethephon, cyclanilide or the like having plant growth regulating effects may be used in combination. 42 318305 200800021 I. Further τ Ben Puming's harmful IT control agent 泰 ▼ is used together with biological pesticides, such as nuclear polyhedrosis virus (NPV), Granulosis virus (Granulosis virus) , GV), Cytoplazmic polyhedrosis virus (CPV), Entomopox virus (EPV) and other viral preparations, Monacrosporium phymatophagum, Steinernema carpocapsae, Steinernema kushidai For the use of insecticidal or nematicidal agents such as Pasteuria penetrans, microbial pesticides, Trichodermalignorum, Agrobacterium radiobacter, and non-pathogenic carrots Erwinia carotovora And biological pesticides such as microbial pesticides used in fungicides such as Bacillus subtilis and Monacrosporium phymatophagum, and herbicides such as Xanthomonas campestris, can be used in combination. And look forward to getting the same fruit.

^ In addition, biological pesticides such as Encarsia W

Formosa), Aphidius colemani, Aphidoletes aphidimyza, Diglyphus isaea, Dacnusa sibirica, Phytoseiulus persimilis, Cucumber blunt (Amblyseius cucumeris), natural enemies such as Oriussauteri, microbial pesticides such as Beauveria brongniartii, (Z)-10-tetradecyl acetate, (E, Z)-4 , 10-tetradecadienyl acetate, (Z)-8-dodecenyl acetate, (Z)-ll-tetradecenyl acetate, (Z)-13-epexene -10-ketone, (Z)_ll-Ten 43 318305 200800021 tetrakilytic acid S, (Z)-13 - 20 fine -10 · 嗣, 14-mercapto-1 - 18 fried and other hormones The pest control agent of the present invention can also be used in combination. DETAILED DESCRIPTION OF THE INVENTION The present invention is exemplified by typical examples and tests, but the invention is not limited thereto. Further, in the examples, the parts are parts by weight. In the examples and the test examples, "(a)" in the table of the "compound (a)" or the test examples means the compound Νο·15 described in Table 1 (that is, the Japanese patent application filed by the researcher of the present invention) Compound No. 448, shown in Table 4 of JP-A-2001-342186, shows a substituted aminoquinazolinone compound. Example 1 Compound (a) 20 parts fenpyroximate 5 parts aqueous citric acid 30 HITENOLN08 (first industrial pharmaceutical product) 5 parts of woody rubic acid word 3 parts A clay hydrating agent 42 parts

W After immersing the active ingredient compound in aqueous dream acid, it is mixed with other ingredients to form a hydrating agent. Example 2 Compound (a) 20 parts of 11 decylamine (tebufenpyrad) 10 parts ΝΡΕ·100 (first industrial pharmaceutical product) 20 parts of propylene glycol 5 parts of Rodolfo 23 (product of Ronald Brown) 2 parts 44 318305 200800021 43 parts of water, the above components are uniformly mixed, and dispersed in water to form a flowable agent. Example 3 Compound (a) 15 parts tebufenzuron 5 parts SP-3005X (Toho Chemicals) 10 parts N-methyl Pyrrolidone 15 parts xylene 55 parts

The above ingredients are mixed and melted to form an emulsion. 20 parts 10 parts 20 parts 2 parts 1 part 47 parts Example 4 Compound (a) Tebufenozide NPE-100 (first industrial pharmaceutical product) Propylene glycol Rodolol 23 water After mixing the above ingredients, the dispersion A flowable agent in water. Example 5 Compound (a) 20 parts of buprofezin 20 parts of water-containing acid 34 parts of HITENOL N08 3 parts of Moer T 2 parts of strontium carbonate powder 21 parts 45 318305 200800021 After the composition of the compound is impregnated with aqueous citric acid , and the ingredients of the ear are mixed to form a hydrating agent. Example 6 Compound (a) 10 parts Tolfenpyrad 10 parts SP-3005X 10 parts N-methylpyrrolidone 15 parts Diphenylbenzene 55 parts The above ingredients were mixed and melted to form an emulsion. Example 7 Compound (a) 20 parts of fluvalinate 10 parts of NPE-100 20 parts of propylene glycol 2 parts of rodolol 23 1 part of water 47 parts The above ingredients were mixed in a uniform example 8 to be dispersed in water to form a flowable Agent. Compound (a> 20 parts chlorfenapyr 10 parts NPE-100 35 parts propylene glycol 3 parts Rodolfo 23 2 parts water 30 parts 46 318305 200800021 ' - Mix the above ingredients one by one, disperse the water; Example 9 Compound (a) 2 parts flubendiamide 1 part clay powder 82 parts diatomaceous earth powder 15 parts Μ test example 1 For the cabbage fruit moth (Plutella xvlostella) and The control effect of Myzus persicae (Myzus persicae) is to mix and pulverize the above ingredients into a powder. The planted cabbage (variety: YR Qingde) is planted in the market, and the number of parasites per 30 plants is investigated after planting for about 1 month. The drug solution was diluted and prepared to have an effective concentration, and the number of parasites per 30 plants was investigated about one week after the dispersion, and the control rate (%) was calculated by the following formula. The results were shown in Table 3. Control rate = 100_{(TaxCb) / (TbxCa)} xl00 φ Ta : number of parasites after treatment in the distribution area

Tb: number of parasites before treatment in the treatment area Ca: number of parasites after dispersal in the treatment area Cb: number of parasites before treatment in the untreated area stems test I 2 for eggplant bolls (Helicoverpa armigera), southern jaundice The control effect of Thrips palmi and Trialeurodes vaporarionim on the number of cotton aphid larvae per 10 strains of eggplant planted in the market (variety: thousand two 2) and the southern yellow pheasant per 100 leaves Number of larvae and temperature 47 318305 200800021 ... The parasite of the whitefly of the whitefly is 1 mesh, after the pan, fully spread the dance to a concentration of the drug solution. One week after the dispersion of the drug solution, the number of cotton bollworm larvae per cockroach and the number of larvae of the yellow cockroach and the number of larvae of the greenhouse whitefly were counted per 100 leaves, and the control rate (%) was calculated according to the following formula. The results are shown in Table 4. 〇 Control rate (%) = 100_{(TaxCb) / (TbxCa)} xl00

Number of parasites after the spread of the Ta·· treatment area

Number of parasites before the spread of Tb·· treatment area # Ca : Number of parasites after dispersal in the treatment area

Cb: Number of pre-spreading parasites in the untreated area Test Example 3 For the control effect of Pseudococcus comstocki and Tetranychus urticae, the apple trees planted in the market were investigated (variety: Fuji, 8 years old) The parasitic number of Kang's whitefly per 20 branches and the number of female adults of the two leaf spiders per 100 leaves, fully diffused to make the effective concentration of the liquid. I then, after 2 weeks of dispersing the drug solution, investigate the parasitic number of each 20 branches of the Kang's powder, and the number of females of the two leaf spiders per 100 leaves after 1, 2, 3, and 4 weeks of dissemination. According to the following formula, the control rate (%) (Kang's whitefly) and the control efficiency (%) (two-point leafhopper) were obtained. The results are shown in Table 5. Control rate (%)=100-{(TaxCb)/(TbxCa)}xl00 Ta : number of parasites after the spread of the treatment zone Tb ··number of parasites before the spread of the treatment zone Ca: post-dispatch parasitization without treatment zone Number of insects Cb: Number of pre-spreading parasites without treatment area 48 318305 200800021 I — — — — rr — — : n ^ Control efficiency (%)={1 -(CtXETa) / (TbXSCa) } X100 \ = I i 552 1 n : number of investigations after dissemination Ta : treatment area after the second survey density Tb: density of the treatment area before the investigation of the density Ca: no treatment area after the distribution of the i-th survey density Cb: before the distribution of the treatment area Investigating Density Test Example 4 For citrus arrow insects (Unaspis yanonensis), φ cotton worms (Aphis gossypii), and hanging orange leaf mites (Panonychus (忭〇 忭〇 防 效果 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 调查 兴 兴 兴 兴Early birth, 8 years old) The number of parasitic females on each 20 branches, the number of cotton aphid parasites, and the number of cotton parasitic insects per 100 leaves and the number of female adults of citrus leaf mites, fully dispersed and diluted Effective concentration of the drug solution. Then, spread 2 stars After the investigation, the number of parasites per 20 branches of the root-web scale insects was won, and the number of cotton mistletoe on every 20 branches after 1, 2, 3, and 4 weeks and the number of female adults of citrus leaf mites per 100 leaves were investigated. The control rate (%) (arrow beetle, cotton aphid) and control efficiency (%) (citrus leafhopper) were calculated according to the same calculation formula above. The results are shown in Table 6. Test Example 5 Rice vertical rolls The control effect of Cnaphalocrocis medinalis and Nilaparuata lugens was transplanted in rice paddy (variety: Koshihikari) in paddy field (mid-May), and in the first half of August, the rice leaf curls were counted in 100 per plant.螟 螟 数 及 及 及 及 及 及 及 及 及 及 及 及 及 及 及 及 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 49 The number of damaged leaves and the number of larvae of brown planthopper were calculated, and the control rate (%) was calculated according to the following formula. The results are shown in Table 7. 〇 control rate (%) = 100-{(TaxCb)/(TbxCa)}xl00

Ta : number of damaged leaves after treatment area / 100 strains of Tb : number of damaged leaves before treatment area / 100 strains of Ca: number of damaged leaves after spreading without treatment area / 100 strains of Cb : scattered leaves before treatment of untreated areas Number / 100 strains • Control rate (%) = 100 - {(TaxCb) / (TbxCa)} xl00

Ta : number of parasites after spreading in the treatment area / 100 strains of Tb : number of pre-spreading parasites in the treatment area / 100 strains of Ca: number of post-spreading parasites without treatment area / 100 strains of Cb: pre-distributed parasites without treatment area The number / 100 of the following list (a) means the compound (a), which is the compound No. 15 in Table 1. In addition, in the table of the test example, "1" is shown, and the test is not performed.

50 318305 200800021 Table 3 Plutella xylostella and nectarines on cabbage, except for the concentration of the test drug (ppm). Control rate (%) Plutella xylostella (a) + fenpyroximate 50+50 94 100 (a) +a than mebendpyrad 50+100 96 100 (a) + tolfenpyrad 50+150 100 100 (a) + buprofezin 50+200 55 100 (a) +tebufenozide 50+100 100 100 (a)+fluvalinate 50+100 60 100 (a)+teflubenzuron 50+25 70 100 (a)+ Fuke (fenobucarb; 50+500 80 100 BPMC) (a) + extepor (isoprocarb; 50+500 70 100 MIPC) (a) + acephate 50+500 100 100 (a) 50 25 100 Fenpu Fenpyroximate 50 45 55 ° than sulphonic acid (tebufenpyrad) 100 55 65 snail snail (tolfenpyrad) 150 97 95 buprofezin 200 0 10 tefenfen (idebufenozide) 100 75 15 Fuhuali ( Fluvalinate) 100 5 100 tebufenzuron 25 15 18 biceps (BPMC) 500 20 50 chlorhexidine (MIPC) 500 20 acephate 500 60 65 51 318305 200800021 Table 4 Eggplant Cotton aphid, Nanhuang Lima and - spilling room-white powder mites except the fruit concentration test concentration (ppm) Helicoverpa armigera South Yellow Stork horse greenhouse whitefly a (a) + fenpyroximate (fenpyroximate) 50+ 50 75 95 100 (a) +n than tebufenpyrad 50+100 80 93 100 (a) + tolfenpyrad 50+150 100 100 100 (a) + teffenozide 50+ 100 100 90 100 (a) + fluvalinate 50+100 80 96 100 (a) + tebufenzuron 50+25 100 93 100 (a) +1 flubendiamide 50 +100 100 97 100 (a)+美他 It milfumimizone 50+250 100 95 100 (a)+funk (fenobucarb; BPMC) 50+500 90 93 100 (a) + exteriz (isoprocarb ; MIPC) 50+500 75 80 100 (a) + acephate 50+500 100 95 100 (a) 50 15 85 100 fenpyroximate 50 30 25 85 ° peamine (tebufenpyrad) 100 35 20 83 ° tolfenpyrad 150 93 90 84 tebufenozide 100 78 18 15 fuvalinate 100 25 85 45 tebufenzuron 25 100 90 16 benzodiazepine (flubendiamide) 100 100 20 12 Methaflumone (me Taflumizone) 250 100 10 10 Fenbubucarb (BPMC) 500 50 80 20 Exoprocarb (MIPC) 500 30 65 20 Acoustic acephate 500 95 90 50 52 318305 200800021 — Table 5 — Apple Shangkang Powder and 2^ Test concentration (ppm) Control rate (%) Conifer powder worm (2) leafhopper (a) + locust amide (tolfenpyrad) 67+150 100 100 (8) + buffing net (buprofezin 67+200 100 60 • (a)+tebufenozide 67+100 100 65 (a)+teflubenzliron 67+50 100 85 (a) 67 100 35 lf 螨 螨 (tolfenpyrad 150 50 65 buprofezin 200 100 10 tebufenozide 100 20 15 teflubenzuron 50 21 35 Table 6 Control of arrow scale insects, cotton aphid and citrus leaf stalks on citrus Effect Test concentration (PPm) Control rate (%) Arrow scale insect cotton citrus leaf 螨 (a) + larvae (tolfenpyrad) 67+150 100 100 85 (8) + buprofezin 67+200 100 100 65 (a) + tebufenozide 67+100 100 100 75 (a) + chlorfenapyr (cMorfenapyr) 67+50 100 100 85 (a) + fuvalinate 67+100 100 100 90 (a) + tebufenzuron 67+25 100 100 85 (a) + flubendiamide 67+100 100 100 90 (8) 67 100 100 25 Tolfenpyrad 150 45 100 65 buprofezin 200 100 20 25 tebufenozide 100 25 25 35 chlorfenapyr 25 45 35 45 fuvalinate 100 43 85 50 tebufenzuron 25 25 28 40 Flubendiamide 100 22 25 30 53 318305 200800021 1 7 Rice industry rice search leafhopper and Fu CZ's anti-effects> Test agent concentration (ppm) Control K%) Rice vertical roll Leaf 螟 飞 ( (a) + buprofezin 50+200 55 100 (a) + tebufenozide 50+100 100 100 (a) + flubendiamide 50+25 100 100 (a) + metaflumizone 50+250 100 100 (a) + fokebucarb (BPMC) 50+500 100 100 (a) + extprozil (MIPC) 50+ 500 100 100 (a) + acephate 50+500 100 100 (a) 50 10 90 buprofezin 200 15 100 tebufenozide 100 100 13 flubendiamide 100 100 35 He It milfumizone 250 100 0 Fenbubucarb (BPMC) 500 90 90 Destruction (isoprocarb; MIPC) 500 90 90 Acetophenes 500 100 80 Test Example 6 For the lush horse (Thrips tabaci丫 control effect I Investigate the number of adult larvae and larvae of the onion and stalks of the scallions (variety: nine onions) planted in the market, and fully spread the diluted solution to become the effective concentration _ the liquid. Then, the number of adult larvae and larvae of each of the 10 plants was counted after 10 days of spreading, and the control rate (%) was calculated according to the following formula. The results are shown in Table 8. 〇 Control rate (%) = 100 - {(TaxCb) / (TbxCa)} xl00 Ta: number of parasites after dispersal in the treatment zone Tb: number of pre-spread parasites in the treatment zone Ca: no treatment zone Number of parasites after dispersal Cb : Number of parasites before dispersal in the treatment area 54 318305 200800021 Table 8 Concentration of the test agent (ppm) of the control group of the green m horses (%) Control rate (%) (a) 100 62 azole alone Tolfenpyrad alone 150 65 (a) + tolfenpyrad 100+150 98 Test Example 7 For the control effect of Frankliniella occidentalis, the eggplant planted in the market : 千二二号) The number of adult larvae and larvae of each of the 10 strains of the western flower, fully dispersed and diluted to become an effective concentration of the drug solution. After 10 days of dissemination, the number of adults and larvae of the western flower thrips was investigated, and the control rate (%) was calculated according to the following formula. The results are shown in Table 9. Control rate (%)=100_{(TaxCb)/(TbxCa)}xl00 Ta : number of parasites after dispersal in the treatment zone Tb: number of pre-spread parasites in the treatment zone Ca: number of parasites after dispersal of the treatment zone A Cb : Number of pre-discretions in the untreated area Table 9 #子上西花 IS horse control effect Test agent concentration (ppm) Control rate (%) (a) Tolfenpyrad alone (tolfenpyrad) alone (a ) + lf 螨 ( ( 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 150 , fully spread with 318305 55 200800021 j diluted to become the effective concentration of the drug solution. Therefore, after I week, I investigated the number of damages caused by #To strains of Liriomyza sativae, and calculated the control rate according to the following formula (%). The results are shown in Table 10. 〇P square removal rate (%) = 10 (HT/C) X100 T: Number of dispersing liquid after treatment area C: Number of untreated area after dispersing liquid medicine Table 10 Control effect of Liriomyza sativae on tomato Test substance concentration (ppm) Control rate (%) (a) Single Use 100 2 locust oleamine (tolfenpyrad) alone with 150 61 (a) + aphid snail (tolfenpyrad) 100+150 90 56 318305

Claims (1)

200800021 '10. Patent application scope ^ ^ ^ 一 ^ 1 · A pest control agent characterized by containing a substituted quinolinone compound and its salts from the following general formula: a compound 'and a compound derived from a compound having insecticidal activity, bactericidal activity or linear killing or two or more compounds as an active ingredient, general formula [I] Wherein R is: (1) a hydrogen atom, (2) a decyl group, (3) a (CVC12) alkyl group, (4) a halogen (CKC6) alkyl group, (5) a (C2-C6) alkenyl group, (6) (CVC6) alkynyl, (7) (CkD sulphur-based, (8) halogen ((VG) sulphur-based, (9) (C-C6) sulphur-based, (i〇) (c3-c6) ring Alkylcarbonyl, | (iiXCkCo alkoxycarbonyl, 318305 57 200800021 (14) Phenyl group, (15) having a halogen atom, a nitro group, a cyano group, a (CVC6) alkyl group, a halogen group (C^C^ a phenylcarbonyl group having 1 to 5 substituents selected from the group consisting of an alkyl group, a (CrQ) alkoxy group, a halogen (CVC6) alkoxy group, a (C!-C6) thiol group, and a halogen (Ci-C6) thiol group. (However, when a plurality of substituents have a plurality of substituents, the substituents may be the same or different), (16) a phenyl (C2-C6) alkenyl group, 10 (17) having a halogen atom, a nitro group, and a cyano group on the ring. , (CVC6) alkyl, halo ((VC6) alkyl, (cKc6) alkoxy, halogen (Cl_c6) alkoxy, (Ci-C6) sulphur-based, halogen (cvc6) sulphur-based and (CkC2) a phenyl (CVC6) alkenyl group having 1 to 5 substituents selected from alkylenedioxy groups (only, when having a plurality of substituents, the substituents may be the same or different), (18) Phenyl (C2-C6) alkynyl, or #U9) having a halogen atom, a nitro group, a cyano group, a (CVC6) group, a halogen (CVC6) group, (Ci-C^) on the ring. Selective 1 to 5 substituents for activating oxygen, pain (CrC^) alkoxy, (Cj-C6) thiol, halogen (CrQ) thio, and (CrC: 2) alkyl dioxy Phenyl (C2_C4) alkynyl (except when a plurality of substituents may be the same or different), R1 represents pyridyl or pyridine-N-oxide, z i_N=c(R2)_ Wherein R 2 represents a hydrogen atom, (CVC: 6) alkyl or halo (Ci_C6) alkyl) or 3) rhyme (in the formula, r 2 * hydrogen atom, (Ci_C6) dazzle 318305 58 200800021 ... Or halogen (C7-C6) alkyl-, 妒 indicates hydrogen wide-hand- or (Ci-Cj 炫基^不· - (1) bromine atom, (2) moth atom, (3) thiophene, (4) ( Ci_C6) thiol, (5) (C2-C6) alkenyl, (6) (C2-C6) alkynyl, 10 (7) halo (Ci-Cg) alkyl, (8) (CVC6) alkoxy, (9) Halogen (CVC6) alkoxy, (10) Halogen (CVCe) sulphur, (11) Halogen (Ci-Cg) sulphate, (12) Halogen (Ci-C6) sill Astragalus, (13) Halogen (Ci-Q) alkoxy halide (CVC 6) alkoxy, • (14) carboxyl, (15XCVC6) alkoxycarbonyl, (16) aminocarbonyl, (17) having (C1:C6)alkyl, (C2-C6)alkenyl and (C2) -C6) an aminocarbonyl group having 1 to 2 substituents selected from alkynyl groups (except that when a plurality of substituents are present, the substituents may be the same or different), (18) phenyl group, (19) having a halogen atom , nitro, cyano, (Cl-C6) alkyl, i (C1 _C6) alkyl, (Ci-Cg) alkoxy, halogen (Ci-Cg) gas 59 318305 200800021 - base, melon to 5 a phenyl group of a substituent (only, when having a plurality of substituents, the substituent may be the same or different), (20) a phenyl (Cr-C3) group, (21) having a halogen atom and a nitro group on the ring , cyano, (Ci_c6) alkyl, halogen (CVC6) alkyl, (CVC6) alkoxy, halogen (cvc6) oxy, (CVC6) alkylthio and halogen (CVC6) alkylthio selected from 1 to a substituted phenyl (Ci-C3) alkyl group of 5 substituents (except that, when having a plurality of substituents, the substituents may be the same or different), (22) phenyloxy, or (23) Halogen atom, nitro group, cyano group, (Ci_C6) alkyl group, a substituted phenyl group having 1 to 5 substituents selected from the group consisting of a halogen (CkC6) alkyl group, a (Cl-C6) alkoxy group, a halogen (Cl-C6) alkoxy group, a (CfC6) thiol group, and a halogen group. An oxy group (except that when a plurality of substituents are present, the substituents may be the same or different), and η is an integer of 1 to 4} 〇2. The pest control agent according to claim 1 of the patent application, wherein Hydrogen atom, (Crc12) alkyl group, (C2-C6&gt; alkenyl group, (C2-C6) alkynyl group, (Ci alkylcarbonyl group, (Cl-C6) alkoxycarbonyl group, or (Cr-C6) alkoxy group (κ3) an alkylcarbonyl group, -Z-R1 represents -NH-CHrRi, or wherein 1 R represents a pyridyl group or a pyridine-N-oxide group, and X represents a bromine atom, an iodine atom, or a halogen (c"c8) Alkyl, (cvq) alkoxy, halogen (CVC6) alkoxy, halogen (cvc6) alkylthio, halogen (CVC6) 318305 60 200800021 alkoxy halide (c "C6" alkoxy tau or TCi ^ 1 An integer of up to 2. .3. The pest control agent according to the scope of the patent application, wherein r represents a (Cl-C6) alkylcarbonyl group, and -Z-R1 represents NH-CHyR1 (wherein Ri represents an acridinyl group), X Shows the tooth (CVC6) alkyl, and n is denoted as 】. / / As claimed in the scope of the patent scope of the pest control agent, wherein the substituted amino quinazolinone compound or its salt is ethoxylated _3,4_ dihydro-3-[(3· -bipyridylmethyl)amino]_6-[1,2,2,2-tetrafluoro_1-(trifluoromethyl)ethyl]-2(1 Η)-quinone or its salts . 5. The pest control agent according to claim 1, wherein the compound having insecticidal activity, acaricidal activity or nematicidal activity is an acetylcholinesterase inhibitor, an acetylcholine receptor inhibitor, GABA regulates chloride channel agonist, sodium channel modulator, nicotine acetylcholine receptor agonist, acetylcholine receptor agonist, chloride channel activator, juvenile hormone mimic, oxidative Phosphorylation inhibitor and Ατρ formation inhibitor, _ oxidative phosphorylation uncoupling agent caused by hydrogen ion gradient disturbance, for Hidadin synthesis inhibitor (type I), quercetin agonist / Peeling inhibitor, octopine amine agonist, position I electron image delivery inhibitor (METI agent), position II electron transport system inhibitor, lipid biosynthesis inhibitor, ryanoprohness regulator or non-specific mechanism of action Compounds such as selective food intake barriers. 6. The pest control agent according to item 1 of the patent application, wherein the compound having the tactile activity, the acaricidal activity or the nematicidal activity is a METI agent, an insecticide, an acaricide, a thiazolidine IGR insecticide. Agent, pyrethroid 318305 61 200800021 一东一系&gt;Insecticide v sodium channel body block insecticide, amine phthalic acid insecticide, organic squamous insecticide, with sputum channel activation Insecticide, phenylmercaptophenone-based insecticide, diterpene-based insecticide. 7. The pest control agent according to claim 1, wherein the compound having insecticidal activity, acaricidal activity or nematicidal activity is acetamiprid, imidacloprid, imidacloprid (imidacloprid) Nitenpyram), thiamethoxam, clothianidin, dinotefuran, thiacloprid, Flonicamid, carbaryl, defec BPMC; fenobucarb), imipenem (MIPC; isoprocarb), ethiofencarb, pirimicarb, oxanyl, benfuracarb, metimocarb, extinction Insect scale (11^〇&1^&111), sulfur enemy (1;1^〇(1^&amp;1*1)), aldicarb, alanycarb, bifen (metolcarb), xylycarb, propoxur, carbofuran, carbosulfan, furathiocarb, amphibious 011 (1〇511) ]^11), aldicarb. - --(aldoxycarb), methomyl, cyhalothrine, perphenazine (permet) Hrin), cypermethrin, bifennin <1>1€611 also 1: 丨11), halfenprox, silafluofen, 赛福宁(〇&gt;^1111:111 ^11), beta-cyfluthrin, tralmethrin, pyrethrin, dextromethrin (&1; 111^11), analin ( Acrinathrin), prallethrin, isofenin 62 318305 200800021 ” Cesmethrin), acetylene OefluthrL·) fenpropathrin, alpha-cypermethrin, race Lamma-cyhalothrin, deltamethrin, fenva-lerate, esfenvalerate, flucythrinate, fluvalinate, fenpropathrin (cycloprothrin), ethofenprox, avermectin, milbemectin, emamectin, spinosad, fenitrothion, marathon (malathion) ), methidathion, fenthion, diazinon, bismuth bowl (ox Ydeprofos), vamidothion, pirimiphos-methyl, chlorpyriphos, terbufos, ethoprophos, cadusafos, fenamiphos, Fensulfothion, DSP, dichlofenthion, fosthiazate, isamidofos, fosthietan, isazofos, valsone (azinphos-methyl), disulfotion, oxydemeton-metliyl, parathions, tebupirimfos, ethion, triclosan (trichlorfon), methamidophos: (metamidophos), dichlorvos, mevinphos, monocrotophos, dimethoate, formetanate, formothion , naled, methylparathion, cyanophos, two meters 63 318305 200800021 ------- _ -^ 广-.1—» — · · -· ' γ%----- v*------ ______ , ------——-- - --- -- --------- —1-- ” ... .............. . diamidafos, propaphos, sulprofos, prothiofos ), profenofos, isofenphos, temephos, phenthoate, dimethylvinphos, chlorfevinphos, tetrachlorvinphos ), phoxim, isoxathion, pyraclofos, chlorpyrifos-methyl, pyridafenthion, phasalone, phasmet, Dioxabenzofos, quinalphos, mesulfenfos, acephate, cartap, thiocyclam, bensultap, sulphur (thiosultap), fenpyroximate, pyridaben, tebufenpyrad, tolfenpyrad, fenazaquin, pyrimidifen, vine (rotenone), hydramethylnon, acequinocyl, 瞒 瞒 旨 | ), fluazinam, flubendiamide, fipronil, acetoprole, ethipiole, eur. - · · * propargite , indoxacarb, meta-miflumizone, quinomethionate, diafenthiuron, cyhextin hydroxide, fenbutatin oxide , amitraz, spirodiclofen, spiromesifen, spirotetramat, chlorfenapyr, baifenke 64 318305 200800021 • — (binapacryl) , chldrbenzilate, phenisobromolate, TPIC, nicotine-sulfate, _ yangmycin (polynactins) complex, azadirachtin, propylpropyl Starch), morantel tartrate, sodium oleate, oleic acid _, pyridalyl, teflubenzuron, chlorfluazuron, diflubenzuron ), hexaflumuron, diquat (novaluron), lufenuron, fluenoxuron, tebufenozide, methoxyfenozide, chromafenozide, halofenozide, two Diofenolan, buprofezin, cyromazine, metoprene, hydroprene, pyriproxyfen, fenoxycarb, pie Pymetrozine, ciofentezine, 赛赛多- * · · (hexythiazox), fenothiocarb, etoxazole, bifenazate, big gram (kelthane; dicofol), benzoximate, tetradifon, dazomet, phosphocarb, levamisol hydrochloride (levamisol HC1) 'abendazole (aibendazole) ), oxibendazole, fenbendazole, oxfendazole, metam-sodium, triazamate or Bacillus thuringiensis; BT ). 8. The pest control agent according to claim 1 of the patent scope, wherein the compound having 65 318305 200800021 L - aerobic activity 'coccidicidal activity or nematode activity - is fenpyroximate, fenobucarb ; BPMC), isopropcarb (MIPC), σ than tebufenpyrad, tolfenpyrad, bupr〇fezin, metaflumizone, defenofol (tebufenozide), chlorfenapyr, fiuvalinate, teflubenzuron or fiubendiamide. The pest control agent according to any one of claims 1 to 8, wherein the substituted amino quinazolinone compound is 1-ethenyl-3,4-dihydrogen -3-[(3_pyridylmethyl)amino]-6·[1,2,2,2-tetrafluoro-1·(trifluoromethyl)ethyl&gt;2(1 Η)·quinazoline Ketones, and compounds having insecticidal activity, acaricidal activity or nematicidal activity are buprofezin, metaflumizone or fiubendiamide. The pest control agent according to any one of claims 1 to 9, wherein the compound has an insecticidal activity and kills relative to 1 part by weight of the substituted aminoquinazolinone compound. The compounding ratio of one or two or more compounds selected from the group consisting of hydrazine active or nematicidal activity is 0.01 to 2000 parts by weight. A method for using a pest control agent, which is characterized in that a pest is protected by a pest, and an effective amount of a pest control agent according to any one of claims 1 to 10 is applied to treat a pest The object is a useful plant, a seed of a useful plant, a soil or a cultivation medium. 12. A pest control method characterized by controlling pests, and the substituted amino quinone 66 318305 200800021 m &quot; sinolinone compound represented by the general formula (I) of claim 1 Selecting one or more compounds from salt scouring, and selecting one or more compounds from compounds having insecticidal activity, acaricidal activity or nematicidal activity as a pest control agent as an active ingredient The effective ingredient amount is measured per 10,000. The use of the compound is the substituted amino quinazoline represented by the general formula (I) in the Jth article of the patent application. One or more compounds selected from the group consisting of a ketone compound and a salt thereof, and are characterized in that it is used for producing a substituted amino-quinazoline toilet compound of the general formula (I) and a salt thereof, which are free from the patent claim 1 One or more compounds selected from the class, and a pest control agent which selects one or more compounds from compounds having insecticidal activity, acaricidal activity or nematicidal activity. 318305 67 200800021 4. Designated representative map: There is no schema in this case (1) The representative representative map of this case is: (). (2) A brief description of the symbol of the representative figure. · 8. If there is a chemical formula in this case, please disclose the chemical formula that best shows the characteristics of the invention: R 4 318305 200800021 Patent Application No. 95121359 (November 14, 1995) 2 1 · A pest control agent characterized by containing one or more compounds selected from the group consisting of substituted amino quinazolinone compounds and salts thereof as shown in the following general formula, and Selecting one or more compounds from compounds having insecticidal activity, acaricidal activity or nematicidal activity as effective Ingredients, General formula [I] {wherein, R is: (1) a hydrogen atom, (2) a fluorenyl group, (3) a (C)-C12) alkyl group, (4) a halogen (CVQ) alkyl group, (5) (C2-C6) alkenyl, (6) (C2-C6) alkynyl, (7) (€νί: 6) alkylthio, (8) halogen (CVC6) alkylthio (9) (CVC6 Alkylcarbonyl, (10) (C3-C6)cycloalkylcarbonyl, 318305 underline 200800021 (11) (c)-c6)l; oxycarbonyl-,--(12) (cvc6) oxygenated Base m group (c]-c3) alkyl group, (13) (Ci-c6) alkoxy group (c)-c3) alkylcarbonyl group, (14) phenyl group, (15) having a halogen atom, a nitrate , cyano, (CVC6) alkyl, functional (CA), (Cl_c6) alkoxy, halogen (Ci_c6) alkoxy, (C]-C6) alkylthio and _(Ci_C6) alkylthio The phenylcarbonyl group of J to 2 substituents is selected (only, when a plurality of substituents are present, the substituents may be the same or different), (16) phenyl (c2-c6) alkenyl group, (17) The ring has a halogen atom, a nitro group, a cyano group, a (C^C6) alkyl group, a (CVC6) alkyl group, a (Cl-C6) alkoxy group, a tooth (Ci-C6) alkoxy group, (cvc: 6) alkylthio, halo(c^-c^)alkylthio and (Ci-C: 2) a phenyl (CVC: 6) fluorenyl group having 1 to 5 substituents selected from the group consisting of alkyl dioxy groups (only, when having a plurality of substituents, the substituents may be the same or different), (18) the group (C2) -C6) a fast group, or (19) having a halogen atom, a nitro group, a cyano group, ([I_c6) alkyl group, a halogen (CfCg) alkyl group, a (CnC6) alkoxy group, a halogen (c^cd) a phenyl (C2_C4) alkynyl group having 1 to 5 substituents selected from the group consisting of an alkoxy group, a (CkC6) thiol group, a halogen (Ci-Q) thiol group and a (CKC2) alkylenedioxy group (only, When a plurality of substituents are used, the substituents may be the same or different), R is a pyridyl or pyridyl oxide group, and z is -N=C(R2)-2 318305 underline 200800021 base or letter (c)- C6)alkyl 'R3 represents a hydrogen atom or (Ci_C6)alkyl group, χ not · t 5 R2 7F A4 ^ 7 (crc6)^^ i (C\-C6m^) or N-CH (RV (in the formula, R2 represents a hydrogen atom, (Ci_C6) burns (1) a bromine atom, (2) an iodine atom, (3) a hydroxyl group, (4) (CVC6) alkyl, (5) (C2-C6) alkenyl, (6) (C2_C6) alkynyl, (7) halogen (CVCs) alkyl, (8) (C!-C6) alkoxy, (9) Halogen (Ci_C6) alkoxy, (10) halogen (CkQ) alkylthio, (11) halogen (C^Q) alkylsulfinyl, (12) from (Ci-CJ) Base, (13) halogen (C "C6" alkoxy!|(Ci_C6) alkoxy, (14) carboxyl, (15) (CVC6) alkoxycarbonyl, (16) amino group, (17) An aminocarbonyl group having 1 to 2 substituents selected from (C)-C6)alkyl, (C2-C6), and (C2-C6)alkynyl groups (in the case of a plurality of substituents, the substitution) The base may be the same or different), (18) phenyl, 3 318305 underline 200800021 (19) having a 7-mercapto group, a cyano group, a (cvc6) fluorenyl group, a _(CkC6) alkyl group, CVC6) a phenyl group having 1 to 5 substituents selected from the group consisting of an alkoxy group, a halogen (CVC6) alkoxy group, a (CrC6) thiol group and a halogen (c)-C6) group (only, having a plurality of substituents) When the substituents may be the same or different, (20) phenyl (CKC3) alkyl, (21) having a halogen atom, a nitrate, a cyano group, a (Cj-Ce) alkyl halide on the ring ( Ci_C 6) a substituted phenyl group of 1 to 5 substituents selected from the group consisting of a base group, (c)-C6) an alkoxy group, a haloalkoxy group, a (CVC6) alkylthio group and a halogen (Cl_C6) alkylthio group (C^) C3) an alkyl group (except that when a plurality of substituents are present, the substituents may be the same or different), (22) a benzyloxy group, or (23) having a halogen atom, a schlossyl group, a nitrogen group, or a (CA) group. Selective i to 5 substituents for the group, the halogen (Cl-C6) alkyl group, the (CI_C6) alkoxy group, the halogen (CVC6) alkoxy group, the (C"C6) thiol &amp; _(Ci_C6) sulphur group Substituted phenyloxy (wherein, with a plurality of substituents, the substituents may be the same or different), an integer from 1 to 4}. , carbonyl, or (CVQ) oxy (Ci_C3) NH-CHrR1, or, in the formula, alkyl, (cKC6) alkoxycarbonyl, or (Ci 3]W05 lined book 4 200800021 / ^ ^ ^ ^ ^^ ^ . iTcT-Ce)^^ . (Ci.C6) alkoxy, halogen (Cl_C6) alkoxy, tooth (CVC6) sulfonyl, halogen (Ci_c6) An alkoxy halide (C)-C6) alkoxy group or a (C)-C6) alkoxy group to give an integer of 1 to 2. 3. The pest control agent according to claim 1 of the patent scope, wherein r represents (CVC6) alkylcarbonyl, · z_Ri represents · nh-c^r, in the formula, reverse] represents money base, X * 4 (Ci_C6) recorded, n each is expressed as! . Spring (such as the pest control agent of the scope of the patent scope, wherein the substituted amino-based sulfonium ketone compound or its salt is i _ ethyl ketone _ 3, heart dihydrogen 3- [( 3. A bit of methyl)aminotetrafluoro]-(trifluoromethyl)ethyl]-2(1 H)-喧 琳 _ _ or its salts. 5. Harmful as claimed in item i: An anti-inhibitor, wherein the compound having insecticidal activity, acaricidal activity or nematicidal activity is an acetaminophen acetal test inhibitor, an acetaminophen receptor inhibitor, a GABA-regulated vapor channel agonist, and a material Difficulty agent, Nicholas Beneficial receptor-sensing effect agent, acetaminophen receptor agonist, chloride channel activator, preservative, sputum, degenerative Weihua inhibitor and ATp Formation of an unblocking agent for oxidative sulphation caused by a hindrance agent and a hydrogen gradient, and a hindrance inhibitor (type 1), a quercetin agonist/peeling inhibitor, and a octopus for Homoptera Amine agonist, position j electron transport system hinder (10): 1), position 11 electron transport system inhibitor, lipid biosynthesis inhibitor, monatinidine receptor modulator or non-specific Mechanism of action (e.g., hindered selective feeding) of the compound. 6. The pest control agent according to item yi of the patent application scope, wherein the compound having the insecticidal activity, the acaricidal activity or the nematicidal activity of the 318305 lined line 5 200800021 is an insecticide, an acaricide, Iridium IGR insecticide, pyrethroid insecticide, sodium channel blocking insecticide, aminocarboxylic acid insecticide, organophosphorus insecticide, killing with calcium channel activation Insecticide, phenylmercaptophenylurea insecticide, diterpene based insecticide. 7. The pest control agent according to claim 1, wherein the compound having insecticidal activity, acaricidal activity or nematicidal activity is acetamiprid, imidacloprid, imidacloprid (imidacloprid) Nitenpyram), thiamethoxam, clothianidin, dinotefuran, thiacloprid, flubendiamide ([1〇111〇&amp;1111(1), Kabbah Carbaryl, Fenbucarb, MIPC; isoprocarb, ethiofencarb, pirimicarb, oxanyl, benfuracarb ,methiocarb, mecarbam, thiodicarb, aldicarb, alanycarb, metolcarb, xylycarb, Propoxur, carbofuran, carbosulfan, furathiocarb, endosulfan, aldoxycarb, methodyl, Cyhalothrine, permethrin, cypermethr In), bifenthrin, halfenprox, silafluofen, cyfluthrin, beta-cyfluthrin, tralmethrin, 6 318305 underline 200800021 pyrethrin, aiiethrin, acrinathrin, praiiethrin, esmethrin, sevoflurane Tefluthrin), fenpropathrin, arsenin (&amp;1卩11&amp;_〇}^卩61&gt;11161:111^11), laminda (lambda-cyhalothrin), deltamethrin, fen芬va_lerate, esfenvalerate, fiucythrinate, fluvaiinate, cycloprothrin, ethofenprox, avermectin , milbemectin, emamectin, spinosad, fenitrothion, marathion, methidathion, fenthion, diazinon ), oxydeprofos, vamidothion, sub Tesong &amp;^11^卩]1〇5-11^化}^1), chlorpyriphos, terfufos, ethoprophos, cadusafos, fensamine 10 (fenamiphos), fensulfothion, DSP, dichlofenthion, fosthiazate, isamidofos, fosthietan, isazofos , azinphos-methyl, disulfotion, oxydemeton-methyl, parathions, tebupirimfos, ethion , trichlorfon, metamidophos, dichlorvos, mevinphos, monocrotophos, dimethoate, annihilation 7 318305 underline 200800021 ( Formetanate), formothion, naled, methylparathion, cyanophos, diamidafos, propaphos, methyl propane sulphide Sulprofos, prothiofos, profenofos, alfifen (isofenphos), temephos, phenthoate, dimethylvinphos, chlorfevinphos, tetrachlorvinphos, phoxim, (phoxim), Isoxathion, pyraclofos, chlorpyrifos-methyl, pyridafenthion, phasalone, phasmet, dioxabenzofos, baiyu Pine (qUinaiph〇s), mesulfenfos, acephate, cartap, thiocyclam, bensultap, thiosultap, fenbuter ( Fenpyroximate), pyripaben, tebufenpyrad, t〇lfenPyrad, scorpion 11 &amp;2&amp;911111, dynasty (卩}^111[(^ 611), rotenone, hydramethylnon, acequinocyl, fiuacrypyrim, fluazinam, fiubendiamide, flubendiamide (fipronil), acetoprole, ethiprole, euro Propargite, indxxacarb, metaflumizone, qUin〇methi〇nate, diafenthiuron, seyheke, cyhextin ) hydroxide, fenbutatin oxide, amitraz, snail | syllabus 31 05 lined 200800021 « (spirodiclofen), quaternone snails (spiromesifen), snails Spirotetramat), chlorfenapyr (〇111 (^£6113)^), binapacryl, chlorbenzilate, phenisobromolate, TPIC, nicotine-sulfate , polynactins complex, azadirachtin, hydroxypropyl starch, morantel tartrate, sodium oleate, potassium oleate, acetamiprid S^ (pyridalyl), teflubenzuron, chlorfluazuron, diflubenzuron, hexaflumuron, n〇valuron, lufenuron, Fluenoxuron, tebufenozide, methoxyfenozi De), chromafenozide, halofenozide, diofenolan, buprofezin, cyromazine, methoprene, methacrylate (11) }^1'〇卩代1^), Pyriproxyfen, fen〇xycarb, pymetrozine, ciofentezine, hexythiazox, Fenothi〇carb, etoxazole, bifenazate, kelthane; dicofol, benzoximate, tetradifon, milong Dazomet), phosphocarb, left 17 m salivasolHCl, albendazole, oxibendazole, fenbendazole, oxfendazole Oxfendazole), metam_sodium, 嗤财威 9 318305 underline 200800021 (triazamate) or Bacillus thuringiensis (BT). 8 · The pest control agent according to claim 1 of the patent scope, wherein the compound having insecticidal activity, bactericidal activity or nematicidal activity is fenpyroximate, fen〇bucarb (BPMC), Isoprocarb (MIPC), η, tebufenpyrad, tolfenpyrad, buprofezin, metaflumizone, tebufenozide, bromo Nitrogen (chlorfenapyr), fluvalinate, teflubenzuron or flubendiamide. The pest control agent according to any one of claims 1 to 8, wherein the substituted aminoquinazolinone compound is 1-ethylmercapto-3,4-dihydro-3 -[(3-Acridinemethyl)amino]-6-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]·2(1Η)_quinazolinone, The compound having insecticidal activity, acaricidal activity or nematicidal activity is buprofezin, metopine, metaflumizone or flubendiamide. The pest control agent according to any one of the items 1 to 9 wherein the substituted amino quinazolinone compound has an insecticidal activity and a bactericidal activity. The compounding ratio of one or more compounds selected from the active or nematicidal activity is 〇1 to 2000 parts by weight. A method for using a pest control agent, which is characterized in that a useful plant is protected from a pest, and an effective amount of a pest control agent according to any one of claims 1 to 10 is applied to treat a target pest or object. A useful plant, a seed of a useful plant, a soil, or a cultivation medium. 10 318305 underline 200800021 12 two pest control methods, which are characterized by pest control, and the substituted amino oxazolinone compounds and their salts as shown in general formula (1) of the scope of patent application i One or more compounds selected from the group consisting of: one or more compounds selected from the group consisting of insecticidal activity, bactericidal activity or nematicidal activity as a pesticidal agent of the active ingredient' , each failure to deal with 01 to brain g. 13. The use of a compound selected from the group consisting of substituted amino quinazolinone compounds of the general formula (I) and salts thereof, and one or more compounds selected from the group consisting of It is characterized in that one or more selected ones of the substituted amino quinazolinone compounds represented by the general formula (1) and the salts thereof, which are contained in the first paragraph of the patent application scope, are selected to have an insecticidal activity. A pest control agent for one or more compounds selected from the group consisting of acaricidal activity or nematicidal activity. One of the pests of the patents, the patent class Bii, the ship type (1), the scorpion ketone compound or its _ face 1 tongue dry, ... shy ^ 1. species above selected suicide insect activity, dodge 栊 ϋ or nematode 2 The compound in the compound of the formula is 盖1 1 2 〇〇〇 盖 盖 盖 二 j j j j j j 选择 选择 选择 选择 选择 选择 选择 选择 选择 选择 选择 选择 选择 选择 选择 选择 选择 具有 具有 具有 具有 具有 具有 具有 具有 具有咐 咐 化合物 其 其 其 其 其 其 其 其 其 其 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐 咐Proportion, add sentence f and 318 318305 line