Quinazolinone compound or salt thereof and preparation method therefor, herbicidal composition, and use thereof

Abstract

The present invention belongs to the technical field of pesticides, and specifically relates to a quinazolinone compound or a salt thereof and a preparation method therefor, a herbicidal composition, and the use thereof. The compound is as represented by general formula (I): wherein Q represents (II); X1, X2, X3, X4, X5 and X6 each independently represent hydrogen, halogen, alkyl, alkenyl, etc.; R1, R2, R3, R5, R6, R8, Y1, Y3, Z1 and Z2 each independently represent hydrogen, halogen, cyano, nitro, alkyl, etc.; and R4, R7 and Y2 each independently represent hydrogen, alkyl, etc. The compound has a good herbicidal activity, is safe to crops, and has a high selectivity.

Description

Quinazolinone compounds or their salts, their preparation methods, herbicidal compositions and applications Technical Field

[0001] This invention belongs to the field of pesticide technology, specifically relating to a quinazolinone compound or its salt, its preparation method, herbicidal composition, and application. Background Technology

[0002] Weed control is a crucial aspect of achieving efficient agriculture. Although a wide variety of herbicides are available on the market, the weed-control performance and crop selectivity of these known compounds are not entirely satisfactory. Furthermore, due to the expanding market, weed resistance, herbicide lifespan, economic considerations, and increasing environmental awareness, scientists need to continuously research and develop new, efficient, safe, economical herbicides with different modes of action. Summary of the Invention

[0003] This invention provides a quinazolinone compound or its salt, a method for preparing the same, a herbicidal composition, and an application thereof. The compound exhibits excellent herbicidal activity, is safe for crops, and has high selectivity.

[0004] The technical solution adopted in this invention is as follows:

[0005] A quinazolinone compound or a salt thereof, as shown in general formula I:

[0006] Where Q represents

[0007] X1, X2, X3, X4, X5, and X6 independently represent hydrogen, halogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl, cycloalkyl, or cycloalkylalkyl, or two substituents on the same carbon atom connected to form =O or unsubstituted or halogen-substituted -(CH2)2-, -(CH2)3-, -(CH2)4-, or -(CH2)5-, or two substituents on different carbon atoms connected to form unsubstituted or halogen-substituted -CH2-, -(CH2)2-, -(CH2)3-, or -(CH2)4-;

[0008] R1, R2, R3, R5, R6, R8, Y1, Y3, Z1, and Z2 independently represent hydrogen, halogen, cyano, nitro, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heterocyclic, aryl, and -OR, respectively. 21 -N(R) 21 )2、-O(CO)N(R 21 )2、-O-alkylene-(CO)R 21 -(CO)OR 21-SR 21 -(SO)R 21 or -(SO2)R 21 Or selected from halogen, cycloalkyl, cycloalkenyl, heterocyclic, aryl, -OR 21 -O-alkylene-OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 An alkyl, alkenyl, or ynyl group substituted with at least one group;

[0009] R4, R7, and Y2 independently represent hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocyclic, or groups selected from cyano, nitro, halogen, cycloalkyl, heterocyclic, aryl, and -OR. 21 -SR 21 -(SO)R 21 or -(SO2)R 21 An alkyl, alkenyl, or ynyl group substituted with at least one group;

[0010] R 21 Each of these can independently represent hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl, cycloalkyl, cycloalkylalkyl, cycloalkenyl, cycloalkenylalkyl, aryl, arylalkyl, heterocyclic or heterocyclic alkyl.

[0011] The aforementioned cycloalkyl, cycloalkenyl, heterocyclic or aryl groups are each independently unsubstituted or substituted by at least one group selected from oxo, halogen, cyano, nitro, alkyl, alkenyl, ynyl, cycloalkyl, haloalkyl, haloalkenyl, haloynyl, halocycloalkyl, alkyl-substituted cycloalkyl, -OR, -SR, -(CO)OR, -(SO2)R or -N(R)2;

[0012] R can independently represent hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl, cycloalkyl, heterocyclic or aryl.

[0013] In one specific embodiment, X1, X2, X3, X4, X5, and X6 independently represent hydrogen, halogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, halogenated C1-C8 alkyl, halogenated C2-C8 alkenyl, halogenated C2-C8 alkynyl, C3-C8 cycloalkyl or C3-C8 cycloalkyl-C1-C8 alkyl, or two substituents on the same carbon atom connected to form =O or unsubstituted or halogenated -(CH2)2-, -(CH2)3-, -(CH2)4- or -(CH2)5-, or two substituents on different carbon atoms connected to form unsubstituted or halogenated -CH2-, -(CH2)2-, -(CH2)3- or -(CH2)4-;

[0014] R1, R2, R3, R5, R6, R8, Y1, Y3, Z1, and Z2 independently represent hydrogen, halogen, cyano, nitro, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, heterocyclic, aryl, and -OR, respectively. 21 -N(R) 21 )2、-O(CO)N(R 21 )2、-O-(C1-C8 alkylene)-(CO)R 21 -(CO)OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 Or selected from halogen, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, heterocyclic, aryl, -OR 21 -O-(C1-C8 alkylene)-OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 C1-C8 alkyl, C2-C8 alkenyl, or C2-C8 alkynyl groups substituted with at least one group;

[0015] R4, R7, and Y2 independently represent hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, aryl, heterocyclic, or groups selected from cyano, nitro, halogen, C3-C8 cycloalkyl, heterocyclic, aryl, and -OR. 21 -SR 21 -(SO)R 21 or -(SO2)R 21 C1-C8 alkyl, C2-C8 alkenyl, or C2-C8 alkynyl groups substituted with at least one group;

[0016] R 21 Each of these can independently represent hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, halo-C1-C8 alkyl, halo-C2-C8 alkenyl, halo-C2-C8 alkynyl, C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C8 alkyl, C3-C8 cycloalkenyl, C3-C8 cycloalkenyl-C1-C8 alkyl, aryl, aryl-C1-C8 alkyl, heterocyclic or heterocyclic-C1-C8 alkyl;

[0017] The aforementioned C3-C8 cycloalkyl, C3-C8 cycloalkenyl, heterocyclic or aryl groups are independently unsubstituted or substituted by at least one group selected from oxo, halogen, cyano, nitro, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 ynyl, C3-C8 cycloalkyl, halo-C1-C8 alkyl, halo-C2-C8 alkenyl, halo-C2-C8 ynyl, halo-C3-C8 cycloalkyl, C3-C8 cycloalkyl substituted with C1-C8 alkyl, -OR, -SR, -(CO)OR, -(SO2)R or -N(R)2;

[0018] R can independently represent hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, halo-C1-C8 alkyl, halo-C2-C8 alkenyl, halo-C2-C8 alkynyl, C3-C8 cycloalkyl, heterocyclic or aryl.

[0019] In another embodiment, X1, X2, X3, X4, X5, and X6 independently represent hydrogen, halogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, halogenated C1-C6 alkyl, halogenated C2-C6 alkenyl, halogenated C2-C6 alkynyl, C3-C6 cycloalkyl or C3-C6 cycloalkyl-C1-C6 alkyl, or two substituents on the same carbon atom connected to form =O or unsubstituted or halogenated -(CH2)2-, -(CH2)3-, -(CH2)4- or -(CH2)5-, or two substituents on different carbon atoms connected to form unsubstituted or halogenated -CH2-, -(CH2)2-, -(CH2)3- or -(CH2)4-;

[0020] R1, R2, R3, R5, R6, R8, Y1, Y3, Z1, and Z2 independently represent hydrogen, halogen, cyano, nitro, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C3-C6 cycloalkenyl, heterocyclic, aryl, and -OR, respectively. 21 -N(R) 21 )2、-O(CO)N(R 21 )2、-O-(C1-C6 alkylene)-(CO)R 21 -(CO)OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 Or selected from halogen, C3-C6 cycloalkyl, C3-C6 cycloalkenyl, heterocyclic, aryl, -OR 21 -O-(C1-C6 alkylene)-OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21C1-C6 alkyl, C2-C6 alkenyl, or C2-C6 alkynyl groups substituted with at least one group;

[0021] R4, R7, and Y2 independently represent hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, aryl, heterocyclic, or groups selected from cyano, nitro, halogen, C3-C6 cycloalkyl, heterocyclic, aryl, and -OR. 21 -SR 21 -(SO)R 21 or -(SO2)R 21 C1-C6 alkyl, C2-C6 alkenyl, or C2-C6 alkynyl groups substituted with at least one group;

[0022] R 21 Each of these can independently represent hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, halo-C1-C6 alkyl, halo-C2-C6 alkenyl, halo-C2-C6 alkynyl, C3-C6 cycloalkyl, C3-C6 cycloalkyl-C1-C6 alkyl, C3-C6 cycloalkenyl, C3-C6 cycloalkenyl-C1-C6 alkyl, aryl, aryl-C1-C6 alkyl, heterocyclic or heterocyclic-C1-C6 alkyl;

[0023] The aforementioned C3-C6 cycloalkyl, C3-C6 cycloalkenyl, heterocyclic or aryl groups are independently unsubstituted or substituted by at least one group selected from oxo, halogen, cyano, nitro, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 ynyl, C3-C6 cycloalkyl, halogenated C1-C6 alkyl, halogenated C2-C6 alkenyl, halogenated C2-C6 ynyl, halogenated C3-C6 cycloalkyl, C3-C6 cycloalkyl substituted with C1-C6 alkyl, -OR, -SR, -(CO)OR, -(SO2)R or -N(R)2;

[0024] R can independently represent hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, halogenated C1-C6 alkyl, halogenated C2-C6 alkenyl, halogenated C2-C6 alkynyl, C3-C6 cycloalkyl, heterocyclic or aryl.

[0025] Furthermore, the salt derivatives are salts commonly used in pesticides, for example, they can be formulated as metal salts, amine salts, sulfonium salts, or phosphorus salts. Alternatively, when a basic moiety is present in the molecule, they can be formulated as salts such as sulfates, hydrochlorides, nitrates, phosphates, etc. These salts are also included in this invention whenever they are used as herbicides for agricultural or horticultural purposes. In this invention, "metal salt" can be, for example, an alkali metal salt, an alkaline earth metal salt, an aluminum salt, or an iron salt. "Alkali metal salt" can be, for example, a sodium salt, a potassium salt, or a lithium salt, preferably a sodium or potassium salt. "Alkaline earth metal salt" can be, for example, a calcium salt or a magnesium salt, preferably a calcium salt. In this invention, "amine salt" can be, for example, an alkyl secondary amine salt, an alkyl tertiary amine salt, or an alkyl quaternary amine salt; an alkanol primary amine salt, an alkanol secondary amine salt, an alkanol tertiary amine salt, or an alkanol quaternary amine salt; an alkyl alkanol primary amine salt, an alkyl alkanol secondary amine salt, an alkyl alkanol tertiary amine salt, or an alkyl alkanol quaternary amine salt; or an alkoxy alkanol primary amine salt, an alkoxy alkanol secondary amine salt, an alkoxy alkanol tertiary amine salt, or an alkoxy alkanol quaternary amine salt, preferably a monoethanolamine salt, a dimethylethanolamine salt, a triethanolamine salt, a dimethylamine salt, a triethylamine salt, an isopropylamine salt, a choline salt, a diethylene glycolamine salt, etc. In this invention, "sulfonium salt" or "phosphonium salt" can be, for example, an alkylsulfonium salt, an alkylphosphonium salt, or an alkanolphosphonium salt.

[0026] In the definitions of compounds shown in the above general formulas and in all the following structural formulas, the technical terms used, whether alone or in compound terms, represent the following substituents: alkyl groups having more than two carbon atoms can be straight-chain or branched. For example, in the compound term "cycloalkylalkyl," the alkyl group can be -CH2-, -CH2CH2-, -CH(CH3)-, -C(CH3)2-, etc. The alkyl group is, for example, C1 alkyl-methyl; C2 alkyl-ethyl; C3 alkyl-propyl such as n-propyl or isopropyl; C4 alkyl-butyl such as n-butyl, isobutyl, tert-butyl, or 2-butyl; C5 alkyl-pentyl such as n-pentyl; C6 alkyl-hexyl such as n-hexyl, isohexyl, and 1,3-dimethylbutyl. Similarly, alkenyl groups are, for example, vinyl, allyl, 1-methylprop-2-en-1-yl, 2-methylprop-2-en-1-yl, but-2-en-1-yl, but-3-en-1-yl, 1-methylbut-3-en-1-yl, and 1-methylbut-2-en-1-yl. Alkynyl groups are, for example, ethynyl, propynyl, but-2-yn-1-yl, but-3-yn-1-yl, and 1-methylbut-3-yn-1-yl. Multiple bonds can be in any position in each unsaturated group. Cycloalkyl groups are carbocyclic saturated ring systems having, for example, three to six carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl. Similarly, cycloalkenyl groups are monocyclic alkenyl groups having, for example, three to six carbon ring members, such as cyclopropenyl, cyclobutenyl, cyclopentenyl, and cyclohexenyl, wherein double bonds can be in any position. Halogens are fluorine, chlorine, bromine, or iodine.

[0027] Unless otherwise specified, the term "aryl" in this invention includes, but is not limited to, phenyl, naphthyl, and... The "heterocyclic group" includes, but is not limited to, saturated or unsaturated non-aromatic cyclic groups. And, including but not limited to, heteroaryl groups, i.e., aromatic cyclic groups containing, for example, 3 to 6 ring atoms and optionally fused with benzo[a] rings, wherein 1 to 4 (e.g., 1, 2, 3, or 4) heteroatoms are selected from oxygen, nitrogen, and sulfur, for example

[0028] The terms "optional" or "optionally" mean that the event or situation described below may or may not occur, and the description includes instances where said event or situation occurs and instances where said event or situation does not occur. For example, the term "optionally...substituted" means that the specified atom or group is unsubstituted or substituted by one or more substituents. If a group is substituted by a group, this should be understood to mean that the group is substituted by one or more groups, either the same or different, selected from those groups mentioned. Furthermore, the same or different substitution characters contained in the same or different substituents are chosen independently and may be the same or different. This also applies to ring systems formed from different atoms and units. Meanwhile, the scope of the claims excludes compounds that are chemically unstable under standard conditions, as known to those skilled in the art.

[0029] Furthermore, unless otherwise specified, "replaced by at least one group" as used in this invention means substituted by, for example, 1, 2, 3, 4, or 5 groups; groups without specific attachment positions (including heterocyclic groups, aryl groups, etc.) can be attached at any position, including positions attached to C or N; if substituted, the substituents can also be substituted at any position, as long as they conform to the rules of chemical bond attachment. For example, a heteroaryl group substituted by one methyl group. Can represent wait.

[0030] Compounds of Formula I, in their respective free or salt forms, and where appropriate, their tautomers, may exist as one of the possible isomers or as mixtures thereof, for example, as pure isomers, such as enantiomers and / or diastereomers, or as mixtures of isomers, such as mixtures of enantiomers, such as racemic mixtures, diastereomer mixtures, or racemic mixtures, depending on the number of asymmetric carbon atoms present in the molecule, their absolute and relative configurations, and / or on the configuration of the non-aromatic double bonds present in the molecule; the present invention relates to these pure isomers and also to all possible mixtures of isomers and should be understood in this sense in each of the above and below, even if stereochemical details are not specifically mentioned in each case. The present invention therefore covers all such isomers and tautomers and mixtures thereof in all proportions, together with isotopic forms, such as deuterated compounds.

[0031] The method for preparing the quinazolinone compound includes the following steps: using the compound... The reaction proceeds as an intermediate, where L represents a leaving group (such as OH, halogen, p-nitrophenoxy, or cyano), and the substituents R1, R2, R3, R4, R5, and R6 are defined as described above.

[0032] In one specific implementation, (1) when the target product is represented by Q When compound I is obtained, compound IV-1 is prepared by condensation reaction of the compound represented by general formula II and the compound represented by general formula III-1, and then compound I-1 is prepared by rearrangement reaction. The reaction equation is as follows:

[0033] (2) When Q represents Compound IV-2 is prepared by a condensation reaction of the compound represented by general formula II and the compound represented by general formula III-2, and then compound I-2 is prepared by a rearrangement reaction. The reaction equation is as follows:

[0034] (3) When Q represents Compound I-3 is prepared by a condensation reaction of the compound represented by general formula II and the compound represented by general formula III-3, and the reaction equation is as follows:

[0035] (4) When Q represents Compound I-4 is prepared by a condensation reaction of the compound represented by general formula II and the compound represented by general formula III-4, and the reaction equation is as follows:

[0036] The definitions of X1, X2, X3, X4, X5, X6, R1, R2, R3, R4, R5, R6, R7, R8, Y1, and Y2 are as described above.

[0037] In one specific embodiment, the condensation reactions in step 1, reaction (3), and (4) are all carried out in the presence of a solvent.

[0038] In one specific embodiment, the rearrangement reaction in Step 2 is carried out in the presence of a catalyst (such as acetone cyanohydrin), a base, and a solvent.

[0039] In another specific embodiment, a condensing agent and / or base are added to the condensation reactions in step 1, reaction (3), and (4).

[0040] In another specific embodiment, the solvent is selected from at least one of aromatic hydrocarbons (such as benzene, chlorobenzene or toluene), N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dichloroethane, dimethyl sulfoxide, 1,4-dioxane, dichloromethane or ethyl acetate.

[0041] In another specific embodiment, the base is selected from at least one of inorganic or organic bases, such as NaH, KH, NaOH, KOH, K2CO3, Na2CO3, NaHCO3, Cs2CO3, KF, CsF, pyrazole, triethylamine, N,N-diisopropylethylamine, pyridine, potassium trimethylsilanol, AcOK, AcONa, MeONa, EtONa, t-BuONa, t-BuOK, etc.

[0042] In another specific embodiment, the condensing agent in step 1, reaction (3) and (4) is selected from at least one of benzotriazine-1-yl-oxytripyrrolidinephosphine hexafluorophosphate (Py-BOP), N,N'-carbonyldiimazole (CDI), 1-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDCI), 1-hydroxybenzotriazole (HOBT), 1,3-dicyclohexylcarbodiimide (DCC) or N,N,N',N'-tetramethyl-O-(7-azabenzotriazine-1-yl)hexafluorophosphate urea (HATU).

[0043] An intermediate, as shown in Formula II.

[0044] A herbicide composition comprising at least one of the quinazolinone compounds in an herbicidal effective amount, preferably further comprising a formulation adjuvant, more preferably further comprising other active ingredients.

[0045] A method for controlling weeds, comprising applying a herbicidally effective amount of at least one of the quinazolinone compounds or the herbicide composition thereon to plants or weedy areas.

[0046] The use of at least one of the quinazoline ketone compounds or the herbicide composition in controlling weeds, preferably, the use of the quinazoline ketone compounds in controlling weeds in useful crops, more preferably, the useful crops include genetically modified crops or crops treated with genome editing technology.

[0047] For many economically important monocotyledonous and dicotyledonous pests, the compounds of Formula I of this invention exhibit outstanding herbicidal activity. The active substances of this invention are also effective against perennial weeds that grow from rhizomes, rootstocks, or other perennial organs and are difficult to control. In this regard, it is generally not important whether the substance is used before sowing, before germination, or after germination. Representative examples of monocotyledonous and dicotyledonous weed populations that can be controlled by the compounds of this invention are specifically mentioned, without limiting the specific species. Examples of weed species to which the active substances are effective include monocotyledons: annuals of *Oat*, *Lolium*, *Alopecurus*, *Fararis*, *Barnyardgrass*, *Digitaria*, *Setaria*, and *Sedge*, and perennials of *Agropyron*, *Cynodon*, *Imperata*, and *Sorghum*, as well as perennials of *Sedge*.

[0048] Regarding dicotyledonous weed species, its effects can be extended to annual species such as *Galium aparine*, *Viola*, *Veronica*, *Sesamum indicum*, *Stellaria*, *Amaranthus*, *Sinapis*, *Ipomoea*, *Heliotropium*, *Chaenomeles*, and *Abutilon*, and perennial weeds such as *Convolvulus*, *Thistle*, *Rumex*, and *Artemisia*. The active substances of this invention effectively control harmful plants such as barnyard grass, *Sagittaria*, *Alisma*, *Eupatorium*, *Sedum*, and *Sedge* under the undetermined condition of rice sowing. If the compounds of this invention are applied to the soil surface before germination, weed seedlings can be completely prevented before they emerge, or growth can be stopped when the weeds develop cotyledons, eventually leading to their complete death after three to four weeks. The compounds of this invention exhibit particularly excellent activity against the following plants: *Apira*, *Sesamum indicum*, *Polygonum cuspidatum*, *Stellaria*, *Veronica ivy*, *Veronica arabiculata*, *Viola tricolor* and *Amaranthus*, *Galium aparine*, and *Kochia scoparia*.

[0049] While the compounds of this invention exhibit excellent herbicidal activity against both monocot and dicot weeds, they cause little to no damage to important economic crops such as wheat, barley, rye, rice, corn, sugar beets, cotton, and soybeans. They are particularly compatible with cereal crops, such as wheat, barley, and corn, especially wheat. Therefore, the compounds of this invention are highly suitable for the selective control of unwanted plants in agricultural or ornamental crops.

[0050] Due to their herbicidal properties, these active substances can be used to control harmful plants in known or future genetically engineered plant cultivation. Transgenic plants typically possess superior traits, such as resistance to specific pesticides, particularly herbicides, and resistance to plant diseases or pathogenic microorganisms, such as specific insects or fungi, bacteria, or viruses. Other specific traits relate to conditions such as quantity, quality, storage stability, composition, and special components of the product. Thus, it is known that transgenic plant products have increased starch content or improved starch quality or different fatty acid compositions.

[0051] The compounds of Formula I of the present invention, or salts thereof, are preferably used in the cultivation of economically important genetically modified crops and ornamental plants, such as cereals, including wheat, barley, rye, oats, millet, rice, cassava, and corn, or in the cultivation of sugar beets, cotton, soybeans, rapeseed, potatoes, tomatoes, peas, and other vegetable plants. The compounds of Formula I are preferably used as herbicides for the cultivation of useful plants that are resistant or have been genetically engineered to be resistant to the toxic effects of the herbicides.

[0052] Traditional methods for breeding plants with improved traits than known plants include, for example, conventional mating methods and mutant breeding. In other words, new plants with improved traits can be obtained using genetic engineering methods (see, for example, EP-0221044 A, EP-0131624 A). Several methods have been described, for example:

[0053] - To improve starch synthesis in plants, genetic engineering is used to modify crop plants (e.g., WO 92 / 11376, WO 92 / 14827, WO 91 / 19806);

[0054] - Transgenic crop plants resistant to specific herbicides, such as glufosinate-methyl (e.g., EP-0242236 A, EP-0242246 A), glyphosate-based herbicides (WO 92 / 00377), or sulfonylurea herbicides (EP-0257993 A, US-5013659 A);

[0055] - For example, genetically modified cotton plants can produce Bt toxins, which can defend against certain pests (EP-0142924 A, EP-0193259 A).

[0056] - A genetically modified crop plant with improved fatty acid composition (WO91 / 13972).

[0057] Many molecular biotechnologies for preparing transgenic plants with improved traits are known (see, for example, Sambrook et al., 1989, Molecular Amplification, Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory, Cold Spring Harbor, New York; or Winnacker, “Gene and Cloning,” VCH Weinheim, 2nd ed., 1996; or Christou, “Trends in Plant Science,” 1 (1996) 423-431). To perform genetic engineering operations, nucleic acid molecules may be introduced into plasmids, resulting in mutations or sequence alterations through DNA sequence recombination. Using standard methods, such as base substitution, removal of portions of the sequence, or addition of natural or synthetic sequences, can be employed. To link DNA fragments together, it is possible to attach conjugates or linkers to the fragments.

[0058] Plant cells containing reduced-activity gene products can be prepared by methods such as expressing at least one appropriate antisense RNA or sense RNA to achieve co-inhibition, or by expressing at least one appropriately constructed ribozyme that specifically cleaves the transcript of the aforementioned gene product.

[0059] For this purpose, it is possible to use a DNA molecule containing the entire coding sequence of the gene product, including any possible flanking sequences, or a DNA molecule containing only a portion of the coding sequence, which must be long enough to achieve an antisense effect in the cell. Alternatively, a sequence that is highly homologous to but not identical to the coding sequence of the gene product can also be used.

[0060] When nucleic acid molecules are expressed in plants, the synthesized proteins can be localized in any desired plant cell compartment. However, to localize in a specific compartment, it is possible, for example, to link the coding region to a DNA sequence to ensure localization at a specific location. These sequences are known to those skilled in the art (see, for example, Braun et al., EMBO J.11 (1992) 3219-3227; Wolter et al., Proc. Natl. Acad. Sci. USA 85 (1988), 846-850; Sonnewald et al., Plant J.1 (1991), 95-106).

[0061] Using known techniques, transgenic plant cells can be recombined into the entire plant. Transgenic plants can be any desired plant variety, i.e., monocots and dicots. In this way, it is possible to obtain transgenic plants with improved traits by overexpressing, inhibiting or suppressing homologous (=natural) genes or gene sequences, or by expressing heterologous (=external) genes or gene sequences.

[0062] When the active substances of this invention are used on genetically modified crops, in addition to the inhibitory effect on harmful plants observed in other crops, they often exhibit specific effects on the corresponding genetically modified crops. For example, they can improve or expand the range of weed control, improve the application rate, preferably combine the herbicide resistance of the genetically modified crop with the performance of the herbicide, and affect the growth and yield of the genetically modified crop. Therefore, this invention also provides the use of the compounds as herbicides to control harmful plants in genetically modified crop plants.

[0063] Furthermore, the compounds of this invention can significantly regulate crop growth. By modulating plant metabolism, these compounds can be used to directionally control plant components and promote harvesting, for example, by causing plant drying and dwarfing. They are also suitable for regulating and inhibiting unwanted plant growth without disrupting crop growth. Inhibiting plant growth plays a crucial role in many monocot and dicot crops because it can reduce or completely prevent lodging.

[0064] The compounds of the present invention can be applied using common formulations, including wettable powders, concentrated emulsions, sprayable solutions, powders, or granules. Thus, the present invention also provides herbicide compositions comprising compounds of formula I. Compounds of formula I can be formulated in various ways depending on typical biological and / or chemical physical parameters. Examples of suitable formulation choices include: wettable powders (WP), water-soluble powders (SP), water-soluble concentrates, concentrated emulsions (EC), emulsions such as oil dispersed in water and water dispersed in oil (EW), sprayable solutions, suspension concentrates (SC), dispersible oil suspensions (OD), suspensions diluted with oil or water, solutions miscible with oil, powders (DP), capsule suspensions (CS), seeddressing compositions, granules for broadcasting and soil application, spray granules, coating granules and absorbent granules, water-dispersible granules (WG), water-soluble granules (SG), ULV (ultra-low volume) formulations, microcapsules, and wax products. These individual formulation types are known and described in the following literature, for example, Winnacker-Küchler, “Chemische Techonologie” [Chemical Processes], Vol. 7, C. Hauser Verlag Munich, 4th ed. 1986; Wade van Valkenburg, “Pesticide Formulations”, Marcel Dekker, NY, 1973; K. Martens, “Spray Drying” Handbook, 3rd ed. 1979, G. Goodwin Ltd. London.

[0065] Necessary formulation adjuvants, such as inert substances, surfactants, solvents, and other additives, are also known and described in the following documents, for example, Watkins's "Handbook of Powder Diluents, Insecticides, and Carriers," 2nd ed., Darland, Caldwell, NJ; Hv01phen's "Introduction to Clay Colloid Chemistry," 2nd ed., J. Wiley and Sons, NY; C. Marsden's "Solvent Guide," 2nd ed., Interscience, NY 1963; McCutcheon's "Annual Report on Detergents and Emulsifiers," MC Publishing, Ridgewood, NJ; Sisley and Wood, "Encyclopedia of Surfactants," Chemical Publishing, NY 1964; of [Ethylene oxide adduct surfactants], Wiss. Verlagagesell. Stuttgart 1976; Winnacker-Küchler, “Chemische Technologie” [Chemical Processes], Vol. 7, C. Hauser Verlag Munich, 4th edition 1986.

[0066] Wettable powders are uniformly dispersible in water and, in addition to the active ingredient, include diluents or inert substances, ionic and nonionic surfactants (wetting agents, dispersants), such as polyethoxyalkylphenols, polyethoxy fatty alcohols, polyoxyethyl aliphatic amines, fatty alcohol polyethylene glycol ether sulfates, alkyl sulfonates, alkyl phenyl sulfonates, sodium lignosulfonate, sodium 2,2'-dinaphthylmethane-6,6'-disulfonate, sodium dibutylnaphthalenesulfonate, or sodium oleoylmethyl taurate. To prepare wettable powders, the active ingredient of the herbicide is finely ground, for example using common equipment such as hammer mills, fan mills, and jet mills, while adjuvants are mixed in simultaneously or sequentially.

[0067] Concentrated emulsions are prepared by dissolving active ingredients in an organic solvent, such as butanol, cyclohexanone, dimethylformamide, xylene, or a mixture of higher-boiling aromatic compounds or hydrocarbons, and then adding one or more ionic and / or nonionic surfactants (emulsifiers). Examples of emulsifiers that can be used include, for example, calcium alkylaryl sulfonate of calcium dodecylbenzenesulfonate, or nonionic emulsifiers such as fatty acid polyethylene glycol esters, alkyl aromatic polyethylene glycol ethers, fatty alcohol polyethylene glycol ethers, propylene oxide-ethylene oxide condensation products, alkyl polyethers, sorbitan esters such as sorbitan fatty acid esters, or polyethylene oxide sorbitan esters such as polyethylene oxide sorbitan fatty acid esters.

[0068] The active substance and finely ground solid material are ground to obtain a powder. The solid material may be talc, natural clay such as kaolin, bentonite, and pyrophyllite, or diatomaceous earth. A water- or oil-based suspension may be prepared, for example, by wet grinding using a commercially available glass bead mill, with or without the addition of a surfactant of the other formulation type mentioned above.

[0069] Emulsions, such as oil-in-water (EW) emulsions, can be prepared using an aqueous organic solvent, a stirrer, a colloid mill, and / or a static mixer, and if necessary, by adding a surfactant of another formulation type as described above.

[0070] Granules can be prepared by spraying the active material onto an adsorbent and granulating it using an inert material, or by concentrating the active material onto the surface of a carrier such as sand or kaolinite and granulating it using a binder such as polyvinyl alcohol, sodium polyacrylate, or mineral oil. Suitable active materials can be granulated using methods for preparing fertilizer granules, and fertilizers can be mixed in if necessary. Aqueous suspension granules can be prepared using conventional methods such as spray-drying, fluidized bed granulation, disc granulation, mixing using a high-speed mixer, and extrusion without solid inert material.

[0071] For methods of preparing granules using grinding discs, fluidized beds, extruders, and spraying, see the following processes, for example, “Spray Drying Handbook,” 3rd edition, 1979, G. Goodwin Ltd., London; J.E. Browning, “Agglomeration,” Chemicals and Engineering, 1967, 147ff; “Perry’s Chemical Engineer’s Handbook,” 5th edition, McGraw-Hill, New York, 1973, 8–57. For information on formulations of crop protection products, see, for example, G.K. C. Lingman, “Weed Control as a Science,” John Wiley and Sons, New York, 1961, 181–96; and JD. F. Greyer, SAEvans, “Weed Control Handbook,” 5th edition, Blackwell Scientific Rublications, Oxford University Press, 1968, 101–103.

[0072] Agricultural chemical formulations typically contain 0.1% to 99%, particularly 0.1% to 95%, of active ingredient Formula I by weight. The concentration of active ingredient in wettable powders is, for example, from about 10% to 99% by weight, with the usual formulation components constituting the remainder to 100% by weight. The concentration of active ingredient in concentrated emulsions can be from about 1% to 90% by weight, preferably 5% to 80%. Powder formulations contain 1% to 30% active ingredient by weight, typically preferably 5% to 20% by weight; however, sprayable solutions contain about 0.05% to 80% by weight, preferably 2% to 50% by weight. The content of active ingredient in aqueous suspension granules depends primarily on whether the active ingredient is liquid or solid, and on the adjuvants, fillers, etc., used during granulation. The content of active ingredient in aqueous suspension granules is, for example, between 1% and 95% by weight, preferably between 10% and 80% by weight.

[0073] The formulation of the active substance may also include thickeners, wetting agents, dispersants, emulsifiers, penetrants, preservatives, antifreeze agents, solvents, fillers, carriers, colorants, defoamers, evaporation inhibitors, and pH and viscosity adjusters that are commonly used in all cases.

[0074] Based on these formulations, they may also be mixed with other pesticide active substances such as insecticides, acaricides, herbicides and fungicides, as well as with safeners, fertilizers and / or plant growth regulators. The mixing method may be pre-mixed or bottled.

[0075] Suitable active substances that can be mixed with the active substances of the present invention in compound formulations or tank-mixed formulations include, for example, known substances in the "World Encyclopedia of New Pesticide Varieties Technology", China Agricultural Science and Technology Press, 2010.9 and the literature cited herein. For example, the following herbicidal active substances can be mixed with compounds of Formula I (Note: the name of the compound is either the common name according to the International Organization for Standardization (ISO) or the chemical name, with a code where appropriate): acetochlor, butachlor, metolachlor, isopropachlor, isopropachlor, succinyl-metolachlor, propachlor, chlorpyrifos, chlorpyrifos, naphthalenepropanoyl-methyl, R-L-naphthalenepropanoyl-methyl, propargyl, benzylthiamethoxam, bisbenzyl-methyl, pyrifluquinazon, chlorpyrifos, flubutyroxychlor, brobutyroxychlor, dimethoate, high-efficiency dimethoate, ethoxybenzyl-methyl, flubutyroxychlor, methoxythiamethoxam, pyrifluquinazon, isoxachlor, high-efficiency methylparaben, high-efficiency methylparaben. Acetaminophen, clethodim, butyrazosulfuron, cyprochloraz, flusulfuron, heptanosulfuron, isobutyrazosulfuron, propyzamide, terbutyrazosulfuron, methylparaben, metolachlor, methylcyclohexane, chlorpyrifos, propyzamide, pendimethalin, carbaryl, succinylmethrin, tricyclomethrin, butyrazosulfuron, succinylmethrin, bensulfuron-methyl, naphthylmethrin, acetochlor, naphthylmethrin, thiamethoxam, pyrimethanil, bensulfuron-methyl, chlorpyrifos, butyrazosulfuron, flupyrazole, atrazine, simazine, promethazine, cypermethrin, cypermethrin, atrazine, pyrazosulfuron, isopropazine, flumethrin, terbutyraz, terbutyraz, triazine flumethrin, cyprochlorazine, glyphosate, chlorpyrifos Phosphatidylcholine, Simazine, Ziziphus jujuba, Dichlorvos, Isoamyl acetate, Cyprodinil, Atrazine, Butyraz, Butyraz, Terbutaline, Methoxypropazine, Cypermethrin, Herbicides, Clonazine, Atrazine, Methoxypropazine, Glycyrrhizin, Cyanobacterium trioxide, Indaziflam, Greensulfuron, Methsulfuron-methyl, Benzylsulfuron, Chlorpyrifos, Bensulfuron-methyl, Thisulfuron-methyl, Pyrimisulfuron-methyl, Methiosulfuron-methyl, Sodium formamide sulfuron, Ethersulfuron-methyl, Etherbensulfuron-methyl, Methsulfuron-methyl, Nicosulfuron-methyl, Aminosulfuron-methyl, Acylsulfuron-methyl, Ethoxysulfuron-methyl, Cyprosulfuron-methyl, Sulfadiazine, Tetraazolidinylsulfuron, Pyrimisulfuron, Monosulfuron-methyl, Fluazolidinylsulfuron, Flupyrimisulfuron, Flupyrimisulfuron, Epimethrin Sulfuric acid, pyrazosulfuron, flusulfuron, propanil, trifluprosulfuron, sulfonylsulfuron, trifluralin, flusulfanil, trifluralin, mesosulfuron sodium salt, flupyrsulfuron, thiosulfuron, pyrimethanil, propyrisulfuron, pyrazosulfuron, trifluralin, flusulfanilamide, quizalofop-p-ethyl, ethoxysulfuron, glufosinate, bensulfuron, chlorfluazuron ethyl, methylfluzoxystrobin, trifluralin, methoxysulfuron, trifluralin, flufenoxuron, flufenoxuron, oxysulfuron, metolachlor, sulfadiazine, flufenoxuron, oxysulfuron, metolachlor, flufenoxuron, flufenoxuron, halosafen, chlormequat chloride, isoproturon, linuron, diuronSaprolegnia, fluroxypyr, bensulfuron, methyl bensulfuron, bensulfuron, sulfothiamethoxam, isoxaflutole, terbutaline, clodinafop-methyl, chlorobromosulfuron, methyl methoxysulfuron, methyl methoxysulfuron, bromosulfuron, methoxysulfuron, chlorpyrifos, metribuzin, cycloroxysulfuron, felsulfuron, flusulfuron, glufosinate, fensulfuron, cyproconazole, thiamethoxam, fensulfuron, chlorpyrifos, methamidophos, thiamethoxam, trimethourea, oxazolium, Monisouron, Anisuron, Methiuron, Chloreturon, tetraflufenozide, betaine, betaine-ethyl, betaine, sulfonamide, terbutaline, fensulfuron-methyl, fensulfuron-methyl, fensulfuron-methyl, fensulfuron-methyl, chlorpyrifos, carboxazo le, Chlorprocarb, Fenasulam, BCPC, CPPC, Carbasulam, Butyrazosulfan, Clethodim, Metrazine, Clethodim, Wild Grass, Permethrin, Clethodim, Barnyardgrass, Cypermethrin, Oat Grass, Dimethoate, Ethylmethazine, Methiobencarb, Clethodim, Benzoate, Methiobencarb, Thionylmethazine, Methiobencarb, 2,4-D Butyl Acetate, 2,4-D Sodium Chloride, 2,4-D Isooctyl Acetate, 2,4-D Sodium Salt, 2,4-D Dimethylamine Salt, 2,4-D Chlorethyl Thiate, 2,4-D Chloride, 2,4-D Propionic Acid, High 2,4-D Propionate, 2,4-D Butyric Acid, 2,4-D Chlorpropionic Acid, 2,4-D Propionate 2,4,5-chlorobutyric acid, 2,4,5-propylpropionic acid, 2,4,5-propylbutyric acid, 2,4,5-chloromethacin, MCPA, dicamba, quizalofop-p-ethyl, cyhalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, cyhalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl, quizalofop-p-ethyl In, proponitrophenol, glyphosate, barnyardphos, glufosinate, methyl parathion, glyphosate, piperazine, diammonium phosphate, dimethoate, phosmet, fenpropathrin, fenpropathrin, fenpropathrin, dimethoate, fenpropathrin, imidacloprid, imidacloprid acetic acid, imidacloprid quinolinic acid, methoxymethylene, methoxymethylene ammonium salt, imidacloprid acetic acid, imidacloprid, clopyralid, clopyralid isooctyl ester, dichloropyridine acid, aminopyridine acid, trichloropyridine acid, fluthion, haloxypyridine, trichloropyridine phenol, thiamethoxam, flupyridine, clopyralid, flupyridine hydrazone, trichloropyridine butoxyethyl ester, cliodinate, clethodim, thiamethoxam, quizalofop-p-ethyl, cyclobenzanone, butenazine, oxadiazine, pyranazine, buthidazole, cyproconazoleAmetridione, Amibuzin, bromobenzonitrile, octanoyl bromobenzonitrile, octanoyl iodobenzonitrile, iodobenzonitrile, diphenylacetonitrile, bispyribac-sodium, hydroxybispyribac-sodium, Iodobonil, pyrimisulfuron-methyl, diflubenzuron, penoxsulam, sulfadiazine, chlorpyrifos-sulfuron-methyl, dichlorvos-sulfuron-methyl, fluroxypyr, bispyribac-sodium, pyrimisulfuron-methyl, pyrimisulfuron-methyl, pyrimisulfuron-methyl, bispyribac-sodium, nicosulfuron-methyl, sulfadiazine, Tembotrione, Tefuryltrione, Bicyclopyrone, Ketospiradox, isoxazolidinone, isoxazolidinone, Fenoxasulfone, M ethiozolin, isopropalazine, pyrazosulfuron, pyrazosulfuron, pyrazosulfuron, bensulfuron, pyrazosulfuron, pyrazosulfuron, pyrazosulfuron, pyrazosulfuron, flumetsulam, pyrazosulfuron, pyrazosulfuron, flumethrin, pyrazosulfuron, flupropacil, pyrazosulfuron, pyrazosulfuron, pyrazosulfuron, flupropacil ... Herbicides, fluazinam, methyl methacrylate, tetrazolium chlorpyrifos, flupyridamole, chlorpyrifos, bromochlor, dimethomorph, pyrazosulfuron, cyprodinil, pyrazosulfuron, pyrazosulfuron, pyrazosulfuron, pyrazosulfuron, cyprodinil, pyrazosulfuron, bentazon, pyrazosulfuron, oxadiazon, cyprodinil, isoxadiazon, cyprodinil, isopropyl methoxysulfuron, cyprodinil, indicarb, sodium chlorate Herbicides, trichloroacetic acid, monochloroacetic acid, hexachloroacetone, tetrafluoropropionic acid, forage grass, bromophenol oxime, triazole sulfonate, methomyl, furazolidone, furazolidone, ethoxysulfuron, pyrimethanil, chlorpyrifos, flurfluthrin, barnyardgrass, acrolein, bensulfuron-methyl, metribuzin, oat ester, thiamethoxam, styracil, hydroxylone, methoxybenzone, pyrimethanil, chlorpyrifos, trichloropropionic acid, Al orac, Diethamquat, Etnipromid, Iprymidam, Ipfencarbazone, Thiencarbazone-methyl, Pyrimisulfan, Chlorflurazole, Tripropindan, Sulglycapin, methylsulfuron, Cambendichlor, Cyproterinic acid, Thiamethoxam, cypermethrin, cypermethrin, cypermethrin, cypermethrin, cypermethrin, cypermethrin, cypermethrin, pyrazole cypermethrin, furazolidone, oxadiazon, bis(oxazolyl)acrylic acid, dichloropropenylamine, fluorochloropyridinium, DOW fluorochloropyridinium, UBH-509D489, LS82-556, KPP-300, NC-324, NC-330, KH-218, DPX-N8189, SC-0744, DOWCO5 35. DK-8910, V-53482, PP-600, MBH-001, KIH-9201, ET-751, KIH-6127 and KIH-2023. ,

[0076] When used, commercially available formulations are diluted in a common manner if necessary, such as with water for wettable powders, concentrated emulsions, suspensions, and granules suspended in water. Powders, granules for soil application, or solutions for broadcasting and spraying generally do not require further dilution with an inert substance before use. The required dosage of Formula I compound varies with external conditions, such as temperature, humidity, and the nature of the herbicide used. It can vary considerably, for example, from 0.001 to 1.0 kg ai / ha, or more active ingredient, but is preferably from 0.005 to 750 g ai / ha, particularly from 0.005 to 250 g ai / ha. Detailed Implementation

[0077] The following examples are for illustrative purposes only and should not be construed as limiting the invention in any way. The scope of protection of this invention is defined by the claims.

[0078] Given the economic efficiency and diversity of the compounds, we preferentially synthesized a number of compounds, some of which are listed in Table 1 below. The specific compound structures and corresponding compound information are shown in Table 1. The compounds in Table 1 are only for better illustration of the present invention and do not limit the invention. Those skilled in the art should not interpret this as limiting the scope of the above-mentioned subject matter of the invention to the following compounds.

[0079] Table 1. Compound structures and their properties 1 H NMR

[0080] Several methods for preparing the compounds of the present invention are described in detail in the following schemes and examples. The raw materials can be commercially available or prepared by methods known in the literature or as detailed in the description. Those skilled in the art will understand that other synthetic routes can also be used to synthesize the compounds of the present invention. Although specific raw materials and conditions in the synthetic routes have been described below, they can be easily replaced with other similar raw materials and conditions. Such variations or modifications to the preparation methods of the present invention, such as various isomers of the compounds, are all included within the scope of the present invention. Furthermore, the preparation methods described below can be further modified according to the disclosure of the present invention using conventional chemical methods well known to those skilled in the art. For example, protecting appropriate groups during the reaction process, etc.

[0081] The following method examples are provided to further illustrate the preparation methods of the present invention. The specific substances, types, and conditions used are intended to further explain the invention and are not intended to limit its reasonable scope. The reagents used in the synthetic compounds shown below are either commercially available or can be easily prepared by those skilled in the art.

[0082] Examples of representative compounds are given below. The synthesis methods of other compounds are similar and will not be described in detail here.

[0083] 1. Synthesis of Compound 6

[0084] (1) Weigh intermediate 6-2 (6.06 g, 21.86 mmol) into a dry gaiwan flask, dissolve it in dichloromethane, add 2-(7-azabenzotriazole)-N,N,N',N'-tetramethylurea hexafluorophosphate (12.47 g, 32.78 mmol), N,N-diisopropylethylamine (8.47 g, 65.57 mmol) and intermediate 6-1 (3.20 g, 24.04 mmol), react for 5 h, monitor the reaction for completeness by LC-MS, pour the system into water, add dichloromethane for extraction, combine the organic phases and dry with anhydrous Na2SO4, concentrate the organic phase, and purify the residue with EA / PE (30-60%) system using Flash to obtain intermediate 6-3, 4.80 g of yellow solid, yield 56.00%, purity 95%.

[0085] (2) Weigh intermediate 6-3 (2.00 g, 5.10 mmol) into a dry eggplant-shaped flask, dissolve it in N,N-dimethylformamide, add trifluoroacetic anhydride (1.07 g, 5.10 mmol) and react for 1 h. After the reaction is completed by LC-MS monitoring, pour the system into water, add ethyl acetate for extraction, combine the organic phases and wash the organic phase three times with saturated brine, dry with anhydrous Na2SO4, concentrate the organic phase to obtain intermediate 6-4, 2.17 g of yellow solid, yield 87.16%, purity 92%.

[0086] (3) Weigh intermediate 6-4 (2.17 g, 4.45 mmol) into a dry eggplant-shaped flask, dissolve it in toluene, add p-toluenesulfonic acid (0.38 g, 2.22 mmol), heat to reflux, and after 5 h of reaction, monitor the reaction to ensure it is complete by LC-MS. Remove toluene, add water and ethyl acetate for extraction, combine the organic phases, dry with anhydrous Na2SO4, concentrate the organic phase, and purify the residue with EA / PE (10-30%) system using Flash to obtain intermediate 6-5 (1.01 g yellow solid, yield 48.33%, purity 97%).

[0087] (4) Weigh intermediate 6-5 (1.00 g, 2.13 mmol) into a dry eggplant-shaped flask. Using tetrahydrofuran as solvent, lower the temperature of the system in an ice bath. Slowly add 2M isopropyl magnesium chloride (1.60 mL, 3.19 mmol). After reacting at 0℃ for 30 min, introduce carbon dioxide gas. After the reaction is complete as monitored by LC-MS, add saturated ammonium chloride solution to quench the reaction. Add water and ethyl acetate for extraction. Dry the organic phase with anhydrous Na2SO4. Concentrate the organic phase. The residue is purified by Flash purification using a dichloromethane / methanol (0-5%) system to obtain intermediate 6-6, a light yellow solid of 0.81 g, with a yield of 98.08% and a purity of 95%.

[0088] (5) Weigh intermediate 6-6 (810 mg, 2.09 mmol) into a dry gai-shaped flask, dissolve it in dichloromethane, add oxaloyl chloride (644 mg, 5.08 mmol), and add 2-3 drops of N,N-dimethylformamide as a catalyst. After reacting for 30 min, remove the solvent from the system by rotary evaporation. Dissolve the obtained solid in an appropriate amount of dichloromethane for later use. Take another dry gai-shaped flask, put in 1,3-cyclohexanedione (341 mg, 3.05 mmol), and add dichloromethane... Dissolve the product in chloromethane, add triethylamine (513 mg, 5.08 mmol), cool the reaction system in an ice bath, and slowly add the prepared acyl chloride dropwise into the system. Remove the ice bath and return the reaction to room temperature. When the reaction stops as monitored by LC-MS, add water and dichloromethane for extraction. Combine the organic phases and dry with anhydrous Na2SO4. Purify the intermediate 6-7 by Flash purification using an EA / PE (10-40%) system to obtain 221 mg of yellow solid, yield 21.96%, purity 97%.

[0089] (6) Weigh intermediate 6-7 (221 mg, 0.46 mmol) into a dry flask, dissolve it in dichloromethane, add triethylamine (92.01 mg, 0.91 mmol) and acetone cyanohydrin (3.08 mg, 0.05 mmol), and react overnight at room temperature. When the reaction stops as monitored by LC-MS, add water and dichloromethane for extraction, combine the organic phases and dry with anhydrous Na2SO4. The target compound 6 is obtained by Flash purification with acetonitrile / water (10-50%) system, yielding 61 mg of yellow solid, with a yield of 27.73% and a purity of 99%.

[0090] 2. Synthesis of Compound 79

[0091] (1) In a 100 mL single-necked flask, 6-3 (2.5 g, 1.0 eq, 6.3 mmol) was dissolved in 20 mL of dichloromethane. 2,2-Difluoropropionic acid (0.83 g, 1.2 eq, 7.56 mmol), pyridine (2.4 g, 5 eq, 31.5 mmol), and phosphorus oxychloride (2.8 g, 3 eq, 18.9 mmol) were added, and the mixture was reacted at room temperature for 2 h. The reaction was confirmed by LCMS. After post-treatment, ethyl acetate and water were added for extraction, and the product was dried to obtain product 79-1 (2.5 g, yield 83%).

[0092] (2) In a 100 mL single-necked flask, 79-1 (2.5 g, 1.0 eq, 5.1 mmol) was dissolved in 25 mL of toluene, and p-toluenesulfonic acid was added as a catalyst. The reaction was carried out at 120 °C for 8 h. The reaction was detected by LCMS. After post-treatment, ethyl acetate and water were added for extraction, dried, and purified in normal phase to obtain product 79-2 (800 mg, yield 33%).

[0093] (3) In a 100 mL single-necked flask, 79-2 (0.8 g, 1.0 eq, 1.7 mmol) was dissolved in 20 mL of N,N-dimethylformamide. Lithium formate (127 mg, 1.5 eq, 2.55 mmol), lithium chloride (107 mg, 1.5 eq, 2.55 mmol), acetic anhydride (350 mg, 2.0 eq, 3.4 mmol), N,N-diisopropylethylamine (438 mg, 2.0 eq, 3.4 mmol), and an appropriate amount of catalyst chlorine (2-dicyclohexylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2'-amino-1,1'-biphenyl)]palladium(II) were added, and the mixture was reacted at 80 °C for 3 h. After the reaction was complete as detected by LCMS, water was added to the reaction solution for post-treatment, the pH was adjusted, back-extracted, dried, and filtered to obtain product 79-3 (600 mg, yield 90%).

[0094] (4) Compound 79-3 (500 mg, 1.30 mmol) was dissolved in dichloromethane, and oxalyl chloride (248 mg, 1.95 mmol) was added. The reaction was carried out at room temperature for 1 hour until the reaction was complete. The solvent was evaporated to dryness to obtain the acyl chloride for later use. 1,3-cyclohexanedione (190 mg, 1.2 eq, 1.7 mmol) was dissolved in 20 mL of dichloromethane, and triethylamine (451 mg, 3 eq, 4.47 mmol) and the above acyl chloride solution were added. The reaction was carried out at room temperature for 4 hours. The reaction was detected by LCMS. After post-treatment, dichloromethane and water were added for extraction, followed by acid washing, drying, and filtration to obtain product 79-4 (600 mg, yield 84%).

[0095] (5) In a 50 mL single-necked flask, 79-4 (600 mg, 1.0 eq, 1.25 mmol) was dissolved in 20 mL of acetonitrile, and triethylamine (378 mg, 3.0 eq, 3.75 mmol) and an appropriate amount of acetone cyanohydrin were added. The reaction was carried out at 40 °C for 8 h. The reaction was detected by LCMS. After post-treatment, dichloromethane and water were added for extraction, acid washing, and reverse phase purification to obtain product 79 (150 mg, yield 25%).

[0096] 3. Synthesis of Compound 82

[0097] (1) Compound 82-1 (4 g, 24.2 mmol) was dissolved in 100 mL of N,N-dimethylformamide, and N-iodosuccinimide (5.25 g, 24.2 mmol) was slowly added in portions at room temperature, and the mixture was stirred for 1 hour. LCMS analysis showed that the starting material was almost completely consumed, and the main peak was the product peak. After adding water to the reaction solution, a solid precipitated out. After filtration and drying, a grayish-white crude solid, 82-2 (4.3 g, 61%), was obtained.

[0098] (2) Compound 82-2 (109 g, 34.2 mmol) was dissolved in 200 mL of dichloromethane. Compound 6-1 (5.0 g, 37.6 mmol) and N,N-diisopropylethylamine (13.2 g, 102 mmol) were added, and the mixture was stirred until homogeneous. Then, 2-(7-azabenzotriazole)-N,N,N',N'-tetramethylurea hexafluorophosphate (15.5 g, 41 mmol) was added, and the mixture was reacted at room temperature for 12 h, with monitoring to ensure complete reaction. The reaction mixture was extracted three times with water and dichloromethane. The combined organic phases were washed three times with saturated sodium chloride solution, dried, and concentrated. Silica gel column chromatography yielded a pale yellow oily compound 82-3 (10.0 g, 66%).

[0099] (3) Compound 82-3 (2.0 g, 4.9 mmol) was dissolved in 50 mL of tetrahydrofuran, stirred until homogeneous, and then acetyl chloride (1.2 g, 14.8 mmol) was added. The reaction was carried out at room temperature for 12 h, and the reaction was monitored to ensure completeness. After evaporation to dryness, crude yellow oily compound 82-4 (2.5 g, 100%) was obtained.

[0100] (4) Compound 82-4 (2.5 g, 5.6 mmol) was dissolved in 50 mL of toluene, and p-toluenesulfonic acid (960 mg, 5.6 mmol) was added. After stirring, the mixture was heated to 120 °C and reacted for 2 h, with the reaction monitored to ensure completeness. The mixture was cooled to room temperature, extracted three times with water and ethyl acetate, and the combined organic phases were washed three times with saturated sodium chloride solution. The mixture was then dried and concentrated. Silica gel column chromatography yielded a pale yellow solid, compound 82-5 (1.8 g, 75%).

[0101] (5) Compound 82-5 (1.2 g, 2.79 mmol) was dissolved in 20 mL of N,N-dimethylformamide, and lithium chloride (236 mg, 5.58 mmol), N,N-diisopropylethylamine (1.08 g, 8.37 mmol), acetic anhydride (836 mg, 8.37 mmol), lithium formate (434 mg, 8.37 mmol), and chloro(2-dicyclohexylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl)[2-(2'-amino-1,1'-biphenyl)]palladium(II) (220 mg, 0.28 mmol) were added sequentially. The mixture was purged with nitrogen three times, stirred thoroughly, and then heated to 70 °C for 4 h. The reaction was monitored to ensure complete reaction. The mixture was cooled to room temperature, extracted once with water and ethyl acetate, and then extracted three times with ethyl acetate after adjusting the aqueous phase to acidity. The combined organic phases were washed three times with saturated sodium chloride solution, dried, and concentrated to give a pale yellow solid compound 82-6 (600 mg, 61%).

[0102] (6) Compound 82-6 (500 mg, 1.36 mmol) was dissolved in dichloromethane, and oxalyl chloride (260 mg, 2.04 mmol) was added. The reaction was carried out at room temperature for 1 hour until complete. The solvent was evaporated to dryness to obtain the acyl chloride for later use. Cyclohexanedione (230 mg, 2.04 mmol) was dissolved in 30 mL of dichloromethane, and triethylamine (410 mg, 4.09 mmol) was added. After stirring thoroughly, the above acyl chloride solution in dichloromethane was added, and the reaction was carried out at room temperature for 12 hours, with the reaction monitored to ensure completeness. The solvent was evaporated to dryness and used directly in the next step.

[0103] (7) Compound 82-7 (400 mg, 0.9 mmol) was dissolved in 20 mL of acetonitrile, and acetone cyanohydrin (5.61 mg, 0.09 mmol) was added. After three N2 displacements, the mixture was heated to 30 °C and stirred overnight. After the reaction was completed, the mixture was quenched with dilute hydrochloric acid, extracted with dichloromethane, and the organic phases were combined. The mixture was washed with saturated brine, dried over anhydrous sodium sulfate, and the organic phase was concentrated. The mixture was then subjected to silica gel column chromatography to obtain a pale yellow oily compound 82 (270 mg, 65%).

[0104] Bioactivity evaluation:

[0105] The activity level standards for plant damage (i.e., growth control rate) are as follows:

[0106] Level 9: Complete death;

[0107] Level 8: Growth control rate is greater than or equal to 90% and less than 100%;

[0108] Level 7: Growth control rate is greater than or equal to 80% and less than 90%;

[0109] Level 6: Growth control rate is greater than or equal to 70% and less than 80%;

[0110] Level 5: Growth control rate is greater than or equal to 50% and less than 70%;

[0111] Level 4: Growth control rate is greater than or equal to 30% and less than 50%;

[0112] Level 3: Growth control rate greater than or equal to 20% and less than 30%;

[0113] Level 2: Growth control rate greater than or equal to 10% and less than 20%;

[0114] Level 1: Growth control rate less than 10%;

[0115] Level 0: No effect.

[0116] The above growth control rates are fresh weight control rates.

[0117] (1) Post-emergence testing experiment:

[0118] Seeds of monocot and dicot weeds, as well as seeds of major crops, were placed in plastic pots filled with soil and covered with 0.5-2 cm of soil. The plants were then allowed to grow in a suitable greenhouse environment. Two weeks after sowing, test plants were treated at the 2-4 leaf stage. The tested compound of this invention was dissolved in acetone, and then Tween 80 was added. Methyl oleate emulsifiable concentrate at a concentration of 900 L / ha was used as a synergist. The solution was diluted with water to a specific concentration and sprayed onto the plants using a spray tower. The plants were then incubated in the greenhouse for two weeks after application. The experiment was repeated three times, and the average value was taken. Representative data are listed in Table 2.

[0119] Table 2 Results of post-emergence weed control experiment Note: N represents no data.

[0120] (2) Water-based closed-loop test:

[0121] Sow weed or crop seeds evenly in muddy soil, let stand in the greenhouse for 1-3 days, then apply the pesticide using a mobile sprayer. Repeat the application three times. After application, keep the soil in muddy state and continue cultivation for about 14 days to observe the weed emergence. The efficacy of the pesticide is evaluated and statistically analyzed. Representative data are listed in Table 3.

[0122] Table 3 Results of the water-based closed-loop test Note: N represents no data.

[0123] Furthermore, numerous tests have revealed that the compounds and compositions described in this invention can control many key grassy weeds, sedges, and broadleaf weeds, including *Amaranthus spp.*, *Eleusine indica*, *Barnyardgrass*, *Veronica persica*, *Solanum nigrum*, *Alopecurus aequalis*, *Lolium spp.*, *Oryza sativa*, *Echinochloa crus-galli*, *Cyperus difformis*, *Polygonum hydropiper*, *Amaranthus urinaria*, and *Monochoria vaginalis*. Tests on peanuts, rice, wheat, and corn under different application methods also demonstrated excellent selectivity and commercial value.

[0124] Finally, it should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention and are not intended to limit it. Although the present invention has been described in detail with reference to preferred embodiments, those skilled in the art should understand that modifications or equivalent substitutions can be made to the technical solutions of the present invention without departing from the spirit and scope of the present invention.

Claims

1. A quinazolinone compound as shown in general formula I, or a salt thereof: in, Q represents X1, X2, X3, X4, X5, and X6 independently represent hydrogen, halogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl, cycloalkyl, or cycloalkylalkyl, or two substituents on the same carbon atom connected to form =O or unsubstituted or halogen-substituted -(CH2)2-, -(CH2)3-, -(CH2)4-, or -(CH2)5-, or two substituents on different carbon atoms connected to form unsubstituted or halogen-substituted -CH2-, -(CH2)2-, -(CH2)3-, or -(CH2)4-; R1, R2, R3, R5, R6, R8, Y1, Y3, Z1, and Z2 independently represent hydrogen, halogen, cyano, nitro, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heterocyclic, aryl, and -OR, respectively. 21 -N(R) 21 )2、-O(CO)N(R 21 )2、-O-alkylene-(CO)R 21 -(CO)OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 Or selected from halogen, cycloalkyl, cycloalkenyl, heterocyclic, aryl, -OR 21 -O-alkylene-OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 An alkyl, alkenyl, or ynyl group substituted with at least one group; R4, R7, and Y2 independently represent hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocyclic, or groups selected from cyano, nitro, halogen, cycloalkyl, heterocyclic, aryl, and -OR. 21 -SR 21 -(SO)R 21 or -(SO2)R 21 An alkyl, alkenyl, or ynyl group substituted with at least one group; R 21 Each of these can independently represent hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl, cycloalkyl, cycloalkylalkyl, cycloalkenyl, cycloalkenylalkyl, aryl, arylalkyl, heterocyclic or heterocyclic alkyl. The aforementioned cycloalkyl, cycloalkenyl, heterocyclic or aryl groups are each independently unsubstituted or substituted by at least one group selected from oxo, halogen, cyano, nitro, alkyl, alkenyl, ynyl, cycloalkyl, haloalkyl, haloalkenyl, haloynyl, halocycloalkyl, alkyl-substituted cycloalkyl, -OR, -SR, -(CO)OR, -(SO2)R or -N(R)2; R can independently represent hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl, cycloalkyl, heterocyclic or aryl.

2. A quinazolinone compound or a salt thereof according to claim 1, characterized in that, X1, X2, X3, X4, X5, and X6 independently represent hydrogen, halogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, halogenated C1-C8 alkyl, halogenated C2-C8 alkenyl, halogenated C2-C8 alkynyl, C3-C8 cycloalkyl or C3-C8 cycloalkyl-C1-C8 alkyl, or two substituents on the same carbon atom connected to form =O or unsubstituted or halogenated -(CH2)2-, -(CH2)3-, -(CH2)4- or -(CH2)5-, or two substituents on different carbon atoms connected to form unsubstituted or halogenated -CH2-, -(CH2)2-, -(CH2)3- or -(CH2)4-; R1, R2, R3, R5, R6, R8, Y1, Y3, Z1, and Z2 independently represent hydrogen, halogen, cyano, nitro, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, heterocyclic, aryl, and -OR, respectively. 21 -N(R) 21 )2、-O(CO)N(R 21 )2、-O-(C1-C8 alkylene)-(CO)R 21 -(CO)OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 Or selected from halogen, C3-C8 cycloalkyl, C3-C8 cycloalkenyl, heterocyclic, aryl, -OR 21 -O-(C1-C8 alkylene)-OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 C1-C8 alkyl, C2-C8 alkenyl, or C2-C8 alkynyl groups substituted with at least one group; R4, R7, and Y2 independently represent hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C8 cycloalkyl, aryl, heterocyclic, or groups selected from cyano, nitro, halogen, C3-C8 cycloalkyl, heterocyclic, aryl, and -OR. 21 -SR 21 -(SO)R 21 or -(SO2)R 21 C1-C8 alkyl, C2-C8 alkenyl, or C2-C8 alkynyl groups substituted with at least one group; R 21 Each of these can independently represent hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, halo-C1-C8 alkyl, halo-C2-C8 alkenyl, halo-C2-C8 alkynyl, C3-C8 cycloalkyl, C3-C8 cycloalkyl-C1-C8 alkyl, C3-C8 cycloalkenyl, C3-C8 cycloalkenyl-C1-C8 alkyl, aryl, aryl-C1-C8 alkyl, heterocyclic or heterocyclic-C1-C8 alkyl; The aforementioned C3-C8 cycloalkyl, C3-C8 cycloalkenyl, heterocyclic or aryl groups are independently unsubstituted or substituted by at least one group selected from oxo, halogen, cyano, nitro, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 ynyl, C3-C8 cycloalkyl, halo-C1-C8 alkyl, halo-C2-C8 alkenyl, halo-C2-C8 ynyl, halo-C3-C8 cycloalkyl, C3-C8 cycloalkyl substituted with C1-C8 alkyl, -OR, -SR, -(CO)OR, -(SO2)R or -N(R)2; R can independently represent hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, halo-C1-C8 alkyl, halo-C2-C8 alkenyl, halo-C2-C8 alkynyl, C3-C8 cycloalkyl, heterocyclic or aryl.

3. A quinazolinone compound or a salt thereof according to claim 1 or 2, characterized in that, X1, X2, X3, X4, X5, and X6 independently represent hydrogen, halogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, halogenated C1-C6 alkyl, halogenated C2-C6 alkenyl, halogenated C2-C6 alkynyl, C3-C6 cycloalkyl or C3-C6 cycloalkyl-C1-C6 alkyl, or two substituents on the same carbon atom connected to form =O or unsubstituted or halogenated -(CH2)2-, -(CH2)3-, -(CH2)4- or -(CH2)5-, or two substituents on different carbon atoms connected to form unsubstituted or halogenated -CH2-, -(CH2)2-, -(CH2)3- or -(CH2)4-; R1, R2, R3, R5, R6, R8, Y1, Y3, Z1, and Z2 independently represent hydrogen, halogen, cyano, nitro, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C3-C6 cycloalkenyl, heterocyclic, aryl, and -OR, respectively. 21 -N(R) 21 )2、-O(CO)N(R 21 )2、-O-(C1-C6 alkylene)-(CO)R 21 -(CO)OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 Or selected from halogen, C3-C6 cycloalkyl, C3-C6 cycloalkenyl, heterocyclic, aryl, -OR 21 -O-(C1-C6 alkylene)-OR 21 -SR 21 -(SO)R 21 or -(SO2)R 21 C1-C6 alkyl, C2-C6 alkenyl, or C2-C6 alkynyl groups substituted with at least one group; R4, R7, and Y2 independently represent hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, aryl, heterocyclic, or groups selected from cyano, nitro, halogen, C3-C6 cycloalkyl, heterocyclic, aryl, and -OR. 21 -SR 21 -(SO)R 21 or -(SO2)R 21 C1-C6 alkyl, C2-C6 alkenyl, or C2-C6 alkynyl groups substituted with at least one group; R 21 Each of these can independently represent hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, halo-C1-C6 alkyl, halo-C2-C6 alkenyl, halo-C2-C6 alkynyl, C3-C6 cycloalkyl, C3-C6 cycloalkyl-C1-C6 alkyl, C3-C6 cycloalkenyl, C3-C6 cycloalkenyl-C1-C6 alkyl, aryl, aryl-C1-C6 alkyl, heterocyclic or heterocyclic-C1-C6 alkyl; The aforementioned C3-C6 cycloalkyl, C3-C6 cycloalkenyl, heterocyclic or aryl groups are independently unsubstituted or substituted by at least one group selected from oxo, halogen, cyano, nitro, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 ynyl, C3-C6 cycloalkyl, halo-C1-C6 alkyl, halo-C2-C6 alkenyl, halo-C2-C6 ynyl, halo-C3-C6 cycloalkyl, C3-C6 cycloalkyl substituted with C1-C6 alkyl, -OR, -SR, -(CO)OR, -(SO2)R or -N(R)2; R can independently represent hydrogen, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, halogenated C1-C6 alkyl, halogenated C2-C6 alkenyl, halogenated C2-C6 alkynyl, C3-C6 cycloalkyl, heterocyclic or aryl.

4. A quinazolinone compound or a salt thereof according to any one of claims 1-3, characterized in that, It is selected from any one of the options in Table 1.

5. A method for preparing a quinazolinone compound or a salt thereof as described in any one of claims 1-4, characterized in that, Includes the following steps: With compounds The reaction is carried out as an intermediate, wherein L represents a leaving group (such as OH, halogen, p-nitrophenoxy or cyano, etc.), and the substituents R1, R2, R3, R4, R5 and R6 are defined as described in any one of claims 1-4.

6. The preparation method according to claim 5, characterized in that, (1) When Q represents Compound IV-1 is prepared by a condensation reaction of the compound represented by general formula II and the compound represented by general formula III-1, and then compound I-1 is prepared by a rearrangement reaction. The reaction equation is as follows: (2) When Q represents Compound IV-2 is prepared by a condensation reaction of the compound represented by general formula II and the compound represented by general formula III-2, and then compound I-2 is prepared by a rearrangement reaction. The reaction equation is as follows: (3) When Q represents Compound I-3 is prepared by a condensation reaction of the compound represented by general formula II and the compound represented by general formula III-3, and the reaction equation is as follows: (4) When Q represents Compound I-4 is prepared by a condensation reaction of the compound represented by general formula II and the compound represented by general formula III-4, and the reaction equation is as follows: The definitions of X1, X2, X3, X4, X5, X6, R1, R2, R3, R4, R5, R6, R7, R8, Y1, and Y2 are as described in claims 1-4; Preferably, the condensation reactions in step 1, reaction (3), and (4) are all carried out in the presence of a solvent, and / or the rearrangement reaction in step 2 is carried out in the presence of a catalyst (such as acetone cyanohydrin), a base, and a solvent. More preferably, a condensing agent and / or a base are added to the condensation reactions in step 1, reaction (3), and (4); More preferably, the solvent is selected from at least one of aromatic hydrocarbons, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dichloroethane, dimethyl sulfoxide, 1,4-dioxane, dichloromethane, or ethyl acetate; the base is selected from at least one of inorganic or organic bases; and / or the condensing agent in step 1, reaction (3), and (4) is selected from at least one of benzotriazol-1-yl-oxytripyrrolidinephosphine hexafluorophosphate, N,N'-carbonyldiimidazole, 1-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride, 1-hydroxybenzotriazole, 1,3-dicyclohexylcarbodiimide, or N,N,N',N'-tetramethyl-O-(7-azabenzotriazol-1-yl)hexafluorophosphate urea.

7. A herbicide composition, characterized in that, The herbicide includes at least one of the quinazolinone compounds or their salts as described in any one of claims 1-4, preferably further comprising formulation adjuvants, and more preferably further comprising other active ingredients.

8. A method for controlling weeds, characterized in that, This includes applying an effective amount of at least one of the quinazolinone compounds or their salts as described in any one of claims 1-4, or the herbicide composition as described in claim 7, to plants or weedy areas.

9. Use of at least one of the quinazolinone compounds or their salts as described in any one of claims 1-4 or the herbicide composition as described in claim 7 for weed control, preferably, the quinazolinone compounds or their salts are used to control weeds in useful crops, more preferably, the useful crops include transgenic crops or crops treated with genome editing technology.

10. An intermediate as described in Formula II of claim 5.

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