Uracil compound containing carboxylate fragment, preparation method therefor, and herbicidal composition and use thereof

Abstract

The present invention relates to the field of pesticide herbicides, and in particular, to a uracil compound containing a carboxylate fragment of formula (I), a preparation method therefor, and a herbicidal composition and use thereof. The uracil compound containing a carboxylate fragment provided by the present invention has better herbicidal activity compared with the prior art. [Image disponible dans le document PDF, Image available in the PDF document]

Description

Uracil Compound Containing Carboxylate Fragment, Preparation Method Therefor, and Herbicidal Composition and Use Thereof TECHNICAL FIELD The present invention relates to the field of pesticide herbicides, and in particular, to a uracil compound containing a carboxylate fragment, a preparation method therefor, and a herbicidal composition and use thereof. BACKGROUND Chemical weed control with herbicides is the most economical and effective means of weed control. However, long-term and continuous use of single varieties or singles mode of action of chemical herbicides in high doses easily lead to problems such as weed resistance and resistance evolution. Development of new varieties of pesticides is a core means to solve the problems. Protoporphyrinogen oxidase (PPO, EC 1.3.3.4) can catalyze oxidation of protoporphyrinogen IX into protoporphyrin IX. The PPO is a key enzyme in the same biosynthetic step of chlorophyll and heme. Inhibiting PPO in plants ultimately leads to accumulation and leakage of substrate protoporphyrin IX into cytoplasm, causing lipid peroxidation of the cytoplasm and albinism and death of the plants. In the past few decades, PPO has been widely studied as an important herbicide target. Studies on uracil compounds as herbicides began in the 1960s and reached a peak in the 1990s. In recent years, few varieties have been developed, and patents reported uracil compounds sometimes. For example, CIBA-GEIGY Company disclosed a structure of the following general formula in US5183492A: [Image disponible dans le document PDF, Image available in the PDF document] After that, Syngenta successfully developed a commercial herbicide Butafenacil (compound 47 in US5183492A), which is mainly used in orchards, including vineyards, cotton fields, and non-cultivated lands to control important gramineous weeds, broad-leaved weeds, sedges, and the like, with good weed control effects. [Image disponible dans le document PDF, Image available in the PDF document] US5183492A also disclosed preparation of benzoyloxy propionate CK (compound 1 in the application) as follows: [Image disponible dans le document PDF, Image available in the PDF document] In summary, existing uracil compound herbicides are relatively single in varieties, with little choice. Therefore, novel uracil herbicides with good herbicidal activity are urgently needed in the market. SUMMARY A technical problem to be solved by the present invention is to provide a novel uracil herbicide with good herbicidal activity. A technical solution for the present invention to solve the above technical problem is as follows: A uracil compound containing a carboxylate fragment, a structure of which is shown in the following general formula (I): [Image disponible dans le document PDF, Image available in the PDF document] in the formula: R1 and R2 are selected from hydrogen or methyl respectively; or R1 and R2 together with the carbon atom they are attached form a 3-membered carbocycle; <semantics>R3<annotation encoding="application / x-tex">R_3< / annotation>< / semantics> is selected from <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> haloalkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkenoxy C1-3 alkyl, C2-6 haloalkenoxy C1-3 alkyl, C2-6 alkynoxy C1-3 alkyl, C2-6 haloalkynoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl <semantics>S(O)n<annotation encoding="application / x-tex">S(O)_n< / annotation>< / semantics> <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C3−6<annotation encoding="application / x-tex">C_{3-6}< / annotation>< / semantics> oxygen-containing cycloalkyl <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, or <semantics>C3−9<annotation encoding="application / x-tex">C_{3-9}< / annotation>< / semantics> oxygen-containing cycloalkyl; n=0, 1, or 2; and when R1 is selected from hydrogen and R2 is selected from methyl, the chiral carbon atom connected thereto may be selected from either an R configuration or an S configuration, or a mixture of the two. According to a preferred compound of the present invention, in the general formula (I): R1 and R2 are selected from hydrogen or methyl respectively; or R1 and R2 together with the carbon atom they are attached form a 3-membered carbocycle; <semantics>R3<annotation encoding="application / x-tex">R_3< / annotation>< / semantics> is selected from <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> haloalkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkenoxy C1-3 alkyl, C2-6 haloalkenoxy C1-3 alkyl, C2-6 alkynoxy C1-3 alkyl, C2-6 haloalkynoxy C1-3 alkyl, C3-6 oxygen-containing cycloalkyl C1-3 alkyl, or C3-9 oxygen-containing cycloalkyl; and when R1 is selected from hydrogen and R2 is selected from methyl, the chiral carbon atom connected thereto may be selected from either an R configuration or an S configuration, or a mixture of the two; and in the mixture, a ratio of R to S is 1:99 to 99:1. According to a more preferred compound of the present invention, in the general formula (I): <semantics>R1<annotation encoding="application / x-tex">R_1< / annotation>< / semantics> and <semantics>R2<annotation encoding="application / x-tex">R_2< / annotation>< / semantics> are selected from hydrogen or methyl respectively; <semantics>R3<annotation encoding="application / x-tex">R_3< / annotation>< / semantics> is selected from <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> haloalkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkenoxy C1-3 alkyl, C2-6 haloalkenoxy C1-3 alkyl, C2-6 alkynoxy C1-3 alkyl, C2-6 haloalkynoxy C1-3 alkyl, C3-6 oxygen-containing cycloalkyl C1-3 alkyl, or C3-9 oxygen-containing cycloalkyl; and when R1 is selected from hydrogen and R2 is selected from methyl, the chiral carbon atom connected thereto may be selected from either an R configuration or an S configuration, or a mixture of the two; and in the mixture, a ratio of R to S is 1:99 to 99:1. In definitions of the compounds of the general formula (I) given above, the used terms are generally defined as follows: Halogen: fluorine, chlorine, bromine, or iodine. Alkyl: linear or branched alkyl, such as methyl, ethyl, propyl, isopropyl, n-butyl, tertiary or secondary butyl, and isomers. Alkenyl: linear or branched alkenes, such as vinyl, 1-propenyl, 2-propenyl, and different butenyl, pentenyl and hexenyl isomers. The alkenyl further includes polyenes, such as 1,2-prodienyl and 2,4-hexadienyl. Alkynyl: linear or branched alkynes, such as ethynyl, propargyl, and different butynyl, pentynyl and hexynyl isomers. The alkynyl further includes polyynes, such as 2,4-hexanediynyl. Alkoxyalkyl: alkyl-O-alkyl-, such as CH3OCH2-. Haloalkoxyalkyl: alkyl-O-alkyl-, on which hydrogen atoms may be partially or completely substituted by halogen atoms, such as ClCH2OCH2-. Alkenoxy: alkenyl-O-alkyl-, such as CH2=CHCH2OCH2CH2-. Haloalkenoxyalkyl: alkenyl-O-alkyl, where O and CH2=CH are not directly connected, and hydrogen atoms on the alkenyls may be partially or completely substituted by halogen atoms, such as ClCH=CHCH2OCH2CH2-. Alkynoxyalkyl: alkynyl-O-alkyl-, such as CH≡CCH2OCH2CH2-, where O and CH≡C are not directly connected. Haloalkynoxyalkyl: alkynyl-O-alkyl-, where hydrogen atoms on the alkynyls may be substituted by halogen atoms, such as ClC=CCH2OCH2CH2-. Alkyl S(O)n alkyl: alkyl-S(O)n-alkyl-, n=0, 1 or 2, such as CH3SCH2CH2-, CH3SOCH2CH2-, and CH3SO2CH2CH2-. Oxygen-containing cycloalkyl: substituted or unsubstituted cyclic [Image disponible dans le document PDF, Image available in the PDF document] oxygen-containing alkyl, such as . Substituent groups include methyl, halogen, cyano, and the like. Oxygen-containing-cycloalkyl-alkyl: substituted or [Image disponible dans le document PDF, Image available in the PDF document] unsubstituted alkyl with cyclic oxygen-containing alkyl, such as , where substituent groups include methyl, halogen, cyano, and the like. Some compounds of the present invention may be described by using specific compounds listed in Table 1, but the present invention is not limited to these compounds. [Image disponible dans le document PDF, Image available in the PDF document] Table 1 [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] [Image disponible dans le document PDF, Image available in the PDF document] A second aspect of the present invention provides a synthetic method for the foregoing uracil compound containing a carboxylate fragment. Specifically, the method includes a contact reaction between the acid compound shown in formula (II) and a different substituted alcohol, halogenated, or sulfonate compound in the 5 presence of a solvent, [Image disponible dans le document PDF, Image available in the PDF document] wherein in the general formulas (I) and (II), definitions of R1, R2, and R3 are the same as defined above. The reaction temperature is 0-160°C, preferably 20-120°C; and the time is 2-15 h, preferably 3-12 h. The reaction solvent is selected from at least one of dichloromethane, 1,2-dichloroethane, tetrahydrofuran, acetonitrile, 1,4-dioxane, toluene, o-xylene, m-xylene, p-xylene, n-heptane, n-octane, and n-nonane. In the reaction, a molar ratio of the carboxylic acid compound shown in formula (II) to the different substituted alcohol, halogenated, or sulfonate compound is 1:(1-4), preferably 1:(1.1-3). Some compounds of the general formula (I) of the present invention may be directly obtained through further esterification of the intermediate 1-8. [Image disponible dans le document PDF, Image available in the PDF document] Intermedia 1-8 Some compounds of the general formula (I) of the present invention may also be esterified directly from the intermediate 1-8 to obtain a carboxylic acid of the general formula (II), or a corresponding ester is hydrolyzed to obtain a carboxylic acid of the general formula (II). The carboxylic acid of the general formula (II) may be further prepared into corresponding acyl chlorides, which are then subjected to contact reactions with different substituted alcohols to obtain some compounds of the general formula (I) of the present invention; the carboxylic acid of the general formula (II) may also be subjected to contact reactions with different substituted alcohols through dehydrating agents to obtain some compounds of the general formula (I) of the present invention; and the carboxylic acid of the general formula (II) may also be subjected to contact reactions with halogenated or sulfonate compounds to obtain some compounds of the general formula (I) of the present invention. [Image disponible dans le document PDF, Image available in the PDF document] The reaction is carried out in an appropriate solvent, and the appropriate solvent may be selected from benzene, toluene, xylene, acetone, tetrahydrofuran, acetonitrile, N,N-dimethylformamide, N-methylpyrrolidone, dichloromethane, chloroform, 1,2-dichloroethane, ethyl acetate, or the like. The reaction may be carried out in the presence or absence of an alkali, and when carried out in the presence of an alkali, the reaction may be accelerated. The alkali may be selected from alkali metal hydrides, such as sodium hydride, lithium hydride, or sodium amide; alkali metal hydroxides, such as sodium hydroxide or potassium hydroxide; alkali metal carbonates, such as sodium carbonate or potassium carbonate; and organic alkalies, such as pyridine, 4-dimethylaminopyridine, triethylamine, N-methylpyrrole, or diisopropylethylamine. When a dehydrating agent is used, the dehydrating agent may be 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride, N,N-dicyclohexylcarbodiimide, or the like. Acyl chlorides may be prepared by using acylation reagents, such as sulfoxide chloride, oxalyl chloride, and the like. The reaction temperature may range from -10°C to a boiling point temperature of the appropriate solvent used in the reaction, generally 0-100°C. The reaction time is from 30 minutes to 20 hours, generally 1-10 hours. R3-X or R3-OH is commercially available. X is a leaving group, and is selected from chlorine, bromine, iodine, or sulfonate. The foregoing method of the present invention may alternatively include necessary pre-treatment operations on the foregoing raw materials and necessary post-treatment operations on reaction products. The operational means of pre-treatment and post-treatment include, but are not limited to, drying, washing, pulping, filtration, centrifugation, column chromatography, recrystallization, and the like. The example section of the present invention provides several specific treatment means, which should not be understood by those skilled in the art as limiting the present invention. Unless otherwise noted, the definitions of groups in the reaction formula are the same as before. A third aspect of the present invention provides a use of the uracil compound containing a carboxylate fragment as a herbicide. A fourth aspect of the present invention provides a herbicidal composition, including a compound of the general formula (I) as an active ingredient, where a weight percentage content of the active ingredient in the composition is 0.1-99.9%. The compound of the present invention has outstanding herbicidal activity against broad-spectrum economically important monocotyledonous and dicotyledonous annual harmful plants, may effectively control a variety of weeds, may achieve good results at low doses, and may be used as a herbicide. Therefore, the present invention further includes a use of the compounds of the general formula (I) in control of weeds. Therefore, the present invention relates to a method for preventing and controlling undesired plants or for regulating plant growth, where one or more compounds of the present invention are applied to plants (for example, harmful plants, such as monocotyledonous or dicotyledonous weeds, or undesired crop plants), seeds (for example, grains, seeds, or asexual propagules, such as tubers or young shoots with buds), or plant growth regions (for example, cultivation regions). The compound of the present invention may be applied before planting (by introduction into soil if appropriate), and before or after seedling. The following examples of various representative monocotyledonous and dicotyledonous weed floras prevented and controlled by the compounds of the present invention are only used to illustrate the present invention, but definitely not limit the present invention. Genera of monocotyledonous harmful plants include Aegilops, Agropyron, Agrostis, Alopecurus, Apera, Avena, Brachiaria, Bromus, Cenchrus, Commelina, Cynodon, Cyperus, Dactyloctenium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristylis, Heteranthera, Imperata, Ischaemum, Leptochloa, Lolium, Monochoria, Panicum, Paspalum, Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria, and Sorghum. Genera of dicotyledonous weeds include Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanes, Artemisia, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia, Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium, Emex, Erysimum, Euphorbia, Galeopsis, Galinsoga, Galium, Hibiscus, Ipomoea, Kochia, Lamium, Lepidium, Lindernia, Matricaria, Mentha, Mercurialis, Mullugo, Myosotis, Papaver, Pharbitis, Plantago, Polygonum, Portulaca, Ranunculus, Raphanus, Rorippa, Rotala, Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea, Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, and Xanthium. When the compound of the present invention is applied to soil before seedling, the growth of harmful plant seeds stops after treatment, and harmful plants stay in a growth period at the time of application, or die completely after a period of time, thereby eliminating competition of weeds harmful to crop plants in a lasting manner at an extremely early time point. When the compound of the present invention is applied to green plant sites after seedling, the growth stops after treatment, and harmful plants stay in a growth period at the time of application, or die completely after a period of time, thereby eliminating competition of weeds harmful to crop plants in a lasting manner at an extremely early time point. Therefore, the technical solution of the present invention further includes a use of the compounds of the general formula (I) in control of weeds. In addition, the compounds of the general formula (I) of the present invention are also applicable to drying and / or defoliation of plants. As mentioned earlier, the present invention provides a pesticide herbicide, which is composed of an active ingredient and excipients, where the active ingredient includes at least one of the foregoing uracil compounds containing a carboxylate fragment. Preferably, the content of the active ingredient in the pesticide herbicide is 0.1-99.9 weight%. The present invention has no special limitations on specific types of the excipients in the herbicide, such as various surfactants and solvents commonly used in the field of herbicides. For example, the uracil compound containing a carboxylate fragment described in the present invention may be dissolved and diluted with a solvent for later use, and a concentration after dissolution and dilution with the solvent is preferably 0.05-0.4 g / L. The solvent for dissolving the uracil compound containing a carboxylate fragment may include at least one of dimethyl sulfoxide and N,N-dimethylformamide, and a reagent for the dilution may be water containing commonly used additives or the like. Preferably, one or more additives commonly used in herbicides in the art, such as surfactants and emulsifiers, may also be added to the solution in which the uracil compound is dissolved. In order to enhance the prevention and control effect of the uracil compound containing a carboxylate fragment described in the present invention and increase a use scope thereof, the uracil compound containing a carboxylate fragment of the present invention may be used alone or used with other commonly used herbicides (such as atrazine, tetrazolyl oxalamide, bromoxynil, cyclopentaoxone, and nitrosulfazone). In addition, the proportion of combined use is not specially limited and may be a conventional proportion in the art, as long as the prevention and control effect after the combined use can be enhanced, the use scope can be increased and the safety can be improved. If there is a conflict between the name of a compound in the present invention and the structural formula, the structural formula shall prevail, except that the structural formula is obviously wrong. The uracil compound containing a carboxylate fragment provided by the present invention has better herbicidal activity compared with the prior art. DETAILED DESCRIPTION OF THE EMBODIMENTS The present invention will be described below in conjunction with examples, but is not limited thereto. In the art, any simple replacement or improvement made by a technician to the present invention falls into the technical solution protected by the present invention. Example 1: Preparation of intermediate 1-8 Step 1: preparation of intermediate 1-1 [Image disponible dans le document PDF, Image available in the PDF document] 20 g of 2-chloro-4-fluorobenzoic acid and 100 g of ethanol were put into a 500 mL four-necked flask, stirred, and cooled to 0°C, and 17.73 g of sulfoxide chloride was slowly added dropwise, where the temperature was maintained below 0°C throughout the process. After the sulfoxide chloride was added, the solution was heated to 75°C and stirred under reflux and reacted overnight, and the reaction solution was spun off to obtain 23.01 g of intermediate 1-1. Step 2: preparation of intermediate 1-2 [Image disponible dans le document PDF, Image available in the PDF document] 67.46 g of intermediate 1-1 and 337.3 g of 1,2-dichloroethane were added to a 1 L four-necked flask and cooled to 0°C, 42.09 g of fuming nitric acid (90%) and 60.12 g of sulfuric acid (98%) were slowly added dropwise, then the solution was slowly heated to room temperature and stirred until the reaction was completed, the reaction solution was transferred to a separating funnel and stood until delamination, an organic phase was taken, an inorganic phase was extracted with 1,2-dichloroethane, the acid in the organic phase was eluted with ice water until the pH value of the aqueous phase was about 7.0, and the solvent was spun off to obtain 89.81 g of crude product. 5 times the mass of n-hexane was added, recrystallization and filtration were carried out, and filter cakes were dried to obtain 42.45 g of intermediate 1-2. Step 3: preparation of intermediate 1-3 [Image disponible dans le document PDF, Image available in the PDF document] 60.84 g of intermediate 1-2, 4.87 g of Pt / C (5%), and 300 mL of ethanol were added into a 1 L autoclave, hydrogen pressure was controlled to 2 MPa, a reaction occurred at 45°C for 11 hours, then the Pt / C was removed by filtration, and the filtrate was spun off to obtain 52.48 g of crude intermediate 1-3. Step 4: preparation of intermediate 1-4 [Image disponible dans le document PDF, Image available in the PDF document] 52.48 g of crude intermediate 1-3, 24.78 g of pyridine, and 262.4 g of dichloromethane were added to a 500 mL four-necked flask and stirred at room temperature, and 34.02 g of ethyl chloroformate was weighed after 5 minutes, diluted with 68.04 g of dichloromethane, and then slowly added dropwise within 1 hour. After reaction for 5 hours, the pH value was adjusted to be weakly acidic, water was added, extraction was carried out with dichloromethane, and the organic phase was spun off to obtain 69.62 g of crude intermediate 1-4. Step 5: preparation of intermediate 1-5 [Image disponible dans le document PDF, Image available in the PDF document] 12.98 g of sodium ethanol was dissolved in 38 g of DMF, stirred, and cooled to 5°C in an ice bath. A DMF (28 g) solution of ethyl 3-amino-4,4,4-trifluorocrotonate (27.95 g) was added dropwise in the ice bath. Then, a DMF solution of 36.84 g of intermediate 1-4 was added dropwise, and the solution was heated to 100°C and stirred for 5 h. After the reaction was completed, the pH value was adjusted to be acidic, extraction was carried out with ethyl acetate, the organic phase was washed with saturated salt water and dried with anhydrous sodium sulfate, the solvent was spun off to obtain 50 g of crude product, and the crude product was purified by column chromatography to obtain 19.05 g of intermediate 1-5. Step 6: preparation of intermediate 1-6 [Image disponible dans le document PDF, Image available in the PDF document] 19.05 g of intermediate 1-5 and 8.287 g of anhydrous potassium carbonate were added to a single-necked flask and dissolved with 60 g of THF, and 7.566 g of dimethyl sulfate was added, followed by stirring overnight at room temperature. After the reaction was completed, the THF was spun off, extraction was carried out with ethyl acetate, the anhydrous sodium sulfate was dried, and the organic phase was spun off to obtain 19.62 g of crude intermediate 1-6. Step 7: preparation of intermediate 1-7 [Image disponible dans le document PDF, Image available in the PDF document] 19.62 g of intermediate 1-6 was dissolved in 150 mL of glacial acetic acid at room temperature, the same volume of 36% hydrochloric acid was added, and a reflux reaction occurred for 8 h. After the reaction was completed, the excess solvent was evaporated under reduced pressure, and water was added to the residue to precipitate solid, followed by stirring and filtration. Filter cakes were washed with water three times, and dried at 60°C to obtain 12.73 g of crude intermediate 1-7. Step 8: preparation of intermediate 1-8 [Image disponible dans le document PDF, Image available in the PDF document] 6.8 g of intermediate 1-7, 35 g of 1,2-dichloroethane, 1 drop of DMF, and 3.316 g of dichlorosulfoxide were added to a 100 ml single-necked flask and subjected to a reflux reaction for 3 h. After the reaction was completed, the excess dichlorosulfoxide and solvent were spun off to obtain 6.22 g of crude intermediate 1-8. Example 2: preparation of compound 3 Step 1: preparation of intermediate 3-1 [Image disponible dans le document PDF, Image available in the PDF document] The intermediate 1-8 (1 g) described in Example 1 and 320 mg of methyl glycolate were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 394 mg of triethylamine was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 1.02 g of intermediate 3-1. Step 2: preparation of intermediate 3-2 [Image disponible dans le document PDF, Image available in the PDF document] 1.02 g of intermediate 3-1, 6.12 g of hydrochloric acid (36%), and 6.12 g of acetic acid were added to a reaction flask and refluxed for 40 min, and the reaction solution was spun off to obtain 1.01 g of intermediate 3-2. Step 3: preparation of intermediate 3-3 [Image disponible dans le document PDF, Image available in the PDF document] 1.01 g of intermediate 3-2, 340 mg of dichlorosulfoxide, 2 drops of DMF, and 5.5 g of dichloroethane were added to a reaction flask, a reflux reaction occurred for 3 h, and the reaction solution was spun off to obtain 1.02 g of intermediate 3-3. Step 4: preparation of compound 3 [Image disponible dans le document PDF, Image available in the PDF document] 103.29 mg of 2-methoxyethanol and 228.95 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 3 mL of dichloromethane solution of the intermediate 3-3 (0.50 g) prepared in the last step was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 165 mg of compound 3. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.16 (d, <semantics>J=7.8<annotation encoding="application / x-tex">J = 7.8< / annotation>< / semantics> Hz, 1H), 7.95 (d, <semantics>J=9.6<annotation encoding="application / x-tex">J = 9.6< / annotation>< / semantics> Hz, 1H), 6.62 (s, 1H), 4.99 (s, 2H), 4.30 – 4.23 (m, 2H), 3.59 – 3.52 (m, 2H), 3.42 (s, 3H), 3.26 (s, 3H). LCMS (ESI) <semantics>[M+H]+=483.05<annotation encoding="application / x-tex">[M + H]^+ = 483.05< / annotation>< / semantics>, Found <semantics>=482.61.<annotation encoding="application / x-tex">=482.61.< / annotation>< / semantics> Example 3: preparation of compound 10 Step 1: preparation of compound 10 [Image disponible dans le document PDF, Image available in the PDF document] 99.83 mg of 2-allyloxyethanol and 123.60 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 2.5 mL of dichloromethane solution of the intermediate 3-3 (0.40 g) described in Example 2 was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 260 mg of light yellow oil as compound 10. 1H NMR (400 MHz, DMSO-d6) δ <semantics>8.16 (d, J=7.7 Hz, 1H),7.94 (d, J=9.6 Hz, 1H),6.61 (s, 1H),5.93−5.72 (m, 1H),<annotation encoding="application / x-tex">8.16 \text{ (d, } J = 7.7 \text{ Hz, } 1\text{H}), 7.94 \text{ (d, } J = 9.6 \text{ Hz, } 1\text{H}), 6.61 \text{ (s, } 1\text{H}), 5.93 - 5.72 \text{ (m, } 1\text{H}),< / annotation>< / semantics> <semantics>5.24 (dq, J=17.4,1.8 Hz, 1H),5.13 (dt, J=10.1,1.6 Hz, 1H),4.99 (s, 2H),4.27 (dd, 1.8 Hz, 1.8 Hz, 1.8 Hz)<annotation encoding="application / x-tex">5.24 \text{ (dq, } J = 17.4, 1.8 \text{ Hz, 1H)}, 5.13 \text{ (dt, } J = 10.1, 1.6 \text{ Hz, 1H)}, 4.99 \text{ (s, 2H)}, 4.27 \text{ (dd, 1.8 Hz, 1.8 Hz, 1.8 Hz)}< / annotation>< / semantics> <semantics>J=5.6,3.6 Hz,2H<annotation encoding="application / x-tex">J = 5.6, 3.6 \text{ Hz}, 2\text{H}< / annotation>< / semantics>), 3.96 (dt, <semantics>J=5.4,1.6 Hz,2H<annotation encoding="application / x-tex">J = 5.4, 1.6 \text{ Hz}, 2\text{H}< / annotation>< / semantics>), 3.67 – 3.55 (m, 2H). LCMS (ESI) <semantics>[M+H]+=509.07<annotation encoding="application / x-tex">[M + H]^+ = 509.07< / annotation>< / semantics>, Found = 508.62. Example 4: preparation of compound 28 Step 1: preparation of compound 28 [Image disponible dans le document PDF, Image available in the PDF document] 95.70 mg of propynol ethoxylate and 148.82 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 3 mL of dichloromethane solution of the intermediate 3-3 (0.50 g) described in Example 2 was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 110 mg of light yellow oil as compound 28. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> <Formule mathématique disponible dans le document PDF, Math available in the PDF document>$8.15 \text{ (d, } J = 7.7 \text{ Hz, } 1\text{H}), 7.94 \text{ (d, } J = 9.6 \text{ Hz, } 1\text{H}), 6.61 \text{ (s, } 1\text{H}), 4.98 \text{ (s, } 2\text{H}), 4.27 \text{ (dd, } 1\text{Hz, } 1\text{Hz, } 1\text{Hz, } 1\text{Hz, } 1\text{Hz, } 1\text{Hz, } 1\text{Hz, } 1\text{Hz, } 1\text{Hz, } 1\text$ <semantics>J=5.7<annotation encoding="application / x-tex">J = 5.7< / annotation>< / semantics>, 3.4 Hz, 2H), 4.16 (d, <semantics>J=2.4<annotation encoding="application / x-tex">J = 2.4< / annotation>< / semantics> Hz, 2H), 3.75 – 3.63 (m, 2H), 3.43 (d, <semantics>J=11.5<annotation encoding="application / x-tex">J = 11.5< / annotation>< / semantics> Hz, 4H). LCMS (ESI) <semantics>[M+H]+=507.05<annotation encoding="application / x-tex">[M + H]^+ = 507.05< / annotation>< / semantics>, Found = 506.83. Example 5: preparation of intermediate 54-3 Step 1: preparation of intermediate 54-1 [Image disponible dans le document PDF, Image available in the PDF document] 20 g of the intermediate 1-8 described in Example 1, 4.86 g of methyl D-lactate, and 100 g of dichloromethane were added to a reaction flask, blown with nitrogen, and stirred at room temperature. 5.9 g of triethylamine was added dropwise within 60 min, followed by stirring overnight at room temperature. After the reaction was completed, column chromatography purification was carried out to obtain 16 g of intermediate 54-1. Step 2: preparation of intermediate 54-2 [Image disponible dans le document PDF, Image available in the PDF document] 15 g of intermediate 54-1, 90 g of hydrochloric acid (36%), and 90 g of acetic acid were added into a reaction flask and stirred at 60°C for 40 min until the reaction ended, and the solvent was spun off to obtain 14 g of intermediate 54-2. Step 3: preparation of intermediate 54-3 [Image disponible dans le document PDF, Image available in the PDF document] 5.0 g of intermediate 54-2,1.63 g of sulfoxide chloride, 25 g of 1,2-dichloroethane, and 2 drops of DMF were added into a reaction flask for reflux stirring at 90°C. After one hour of reaction, the solvent was spun off to obtain 5.1 g of intermediate 54-3. Example 6: preparation of compound 54 [Image disponible dans le document PDF, Image available in the PDF document] 0.6 g of the intermediate 54-3 described in Example 5, 0.120 g of 2-methoxyethanol, 10 g of dichloromethane, and 0.2 g of triethylamine were added to a reaction flask, blown with nitrogen, and stirred at room temperature for 1 h until the reaction ended. After the reaction was completed, column chromatography purification was carried out to obtain 0.350 g of compound 54. 1H NMR (400 MHz, CDCl3) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (dd, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics>, 2.0 Hz, 1H), 7.40 (d, <semantics>J=9.2<annotation encoding="application / x-tex">J = 9.2< / annotation>< / semantics> Hz, 1H), 6.37 (s, 1H), 5.36 (q, <semantics>J=7.0 Hz<annotation encoding="application / x-tex">J = 7.0 \text{ Hz}< / annotation>< / semantics>, 1H), 4.32 (s, 2H), 3.60 (t, <semantics>J=4.6 Hz<annotation encoding="application / x-tex">J = 4.6 \text{ Hz}< / annotation>< / semantics>, 2H), 3.57 (s, 3H), 3.36 (s, 3H), 1.62 <semantics>(d,J=7.1 Hz,3H)<annotation encoding="application / x-tex">(d, J = 7.1 \text{ Hz}, 3\text{H})< / annotation>< / semantics>. LCMS (ESI) <semantics>[M+H]+=497.07<annotation encoding="application / x-tex">[M + H]^+ = 497.07< / annotation>< / semantics>, Found = 497.16. Example 7: preparation of compound 61 Step 1: preparation of compound 61 [Image disponible dans le document PDF, Image available in the PDF document] 290 mg of 2-allyloxyethanol and 330 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 10 mL of dichloromethane solution of the intermediate 54-3 (1.0 g) described in Example 5 was added dropwise, and then a reaction occurred at room temperature for 1 h. After the reaction was completed, column chromatography purification was carried out to obtain 800 mg of compound 61. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.14 (d, <semantics>J=7.8<annotation encoding="application / x-tex">J = 7.8< / annotation>< / semantics> Hz, 1H), 7.94 (d, <semantics>J=9.6<annotation encoding="application / x-tex">J = 9.6< / annotation>< / semantics> Hz, 1H), 6.62 (d, <semantics>J=3.0<annotation encoding="application / x-tex">J = 3.0< / annotation>< / semantics> Hz, 1H), 5.84 (ddtd, <semantics>J=16.9<annotation encoding="application / x-tex">J = 16.9< / annotation>< / semantics>, 10.6, 5.3, 1.1 Hz, 1H), 5.31 (qt, <semantics>J=6.5<annotation encoding="application / x-tex">J = 6.5< / annotation>< / semantics>, 3.3 Hz, 1H), 5.26 – 5.20 (m, 1H), 5.12 (dq, <semantics>J=10.4<annotation encoding="application / x-tex">J = 10.4< / annotation>< / semantics>, 1.6 Hz, 1H), <semantics>4.34−4.20<annotation encoding="application / x-tex">4.34 - 4.20< / annotation>< / semantics> (m, 2H), <semantics>3.95<annotation encoding="application / x-tex">3.95< / annotation>< / semantics> (dt, <semantics>J=5.3<annotation encoding="application / x-tex">J = 5.3< / annotation>< / semantics>, <semantics>1.5<annotation encoding="application / x-tex">1.5< / annotation>< / semantics> Hz, 2H), <semantics>3.60<annotation encoding="application / x-tex">3.60< / annotation>< / semantics> (ddd, <semantics>J=6.0<annotation encoding="application / x-tex">J = 6.0< / annotation>< / semantics>, <semantics>4.2<annotation encoding="application / x-tex">4.2< / annotation>< / semantics>, 1.4 Hz, 2H), <semantics>3.45−3.40<annotation encoding="application / x-tex">3.45 - 3.40< / annotation>< / semantics> (m, 3H), <semantics>1.53<annotation encoding="application / x-tex">1.53< / annotation>< / semantics> (d, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 3H).LCMS (ESI) [M + H]+ =523.08, Found =522.96. Example 8: preparation of compound 79 Step 1: preparation of compound 79 [Image disponible dans le document PDF, Image available in the PDF document] 1 g of the intermediate 54-3 described in Example 5 was dissolved in 5 mL of 1,2-dichloroethane, a 1,2-dichloroethane solution of propynol ethoxylate (220 mg) was added dropwise, the solution was stirred at 20°C for 10 minutes, and then 330 mg of triethylamine was added dropwise. After the reaction of the raw materials was completed upon LCMS test, 20 mL of hydrochloric acid (1N) was added for washing, the solution was separated, the organic phase was dried with anhydrous sodium sulfate, and column chromatography purification was carried out to obtain 200 mg of colorless oily liquid as compound 79. 1H NMR (400 MHz, Chloroform-d) δ 7.97 (dd, <semantics>J=7.7,2.1 Hz,1H),7.40 (d, J=9.2 Hz,1H),6.38 (d, J=1.0 Hz,1H),5.36 (q, J=7.1 Hz,1H),5.36 (q, J=7.1 Hz,1H),5.36 (q, J=7.1 Hz,1H),5.36 (q, J=7<annotation encoding="application / x-tex">J = 7.7, 2.1 \text{ Hz}, 1H), 7.40 \text{ (d, } J = 9.2 \text{ Hz}, 1H), 6.38 \text{ (d, } J = 1.0 \text{ Hz}, 1H), 5.36 \text{ (q, } J = 7.1 \text{ Hz}, 1H), 5.36 \text{ (q, } J = 7.1 \text{ Hz}, 1H), 5.36 \text{ (q, } J = 7.1 \text{ Hz}, 1H), 5.36 \text{ (q, } J = 7< / annotation>< / semantics> Hz, 1H), 5.30 (s, 1H), 4.17 (dd, <semantics>J=2.4<annotation encoding="application / x-tex">J = 2.4< / annotation>< / semantics>, 0.7 Hz, 2H), 3.76 (dt, <semantics>J=6.9<annotation encoding="application / x-tex">J = 6.9< / annotation>< / semantics>, 3.0 Hz, 2H), <semantics>3.59−3.55<annotation encoding="application / x-tex">3.59 - 3.55< / annotation>< / semantics> (m, 3H), <semantics>1.62<annotation encoding="application / x-tex">1.62< / annotation>< / semantics> (dd, <semantics>J=7.1<annotation encoding="application / x-tex">J = 7.1< / annotation>< / semantics>, <semantics>1.0<annotation encoding="application / x-tex">1.0< / annotation>< / semantics> Hz, 3H), <semantics>1.33−1.23<annotation encoding="application / x-tex">1.33 - 1.23< / annotation>< / semantics> (m, 2H). LCMS (ESI) <semantics>[M+H]+=521.07<annotation encoding="application / x-tex">[M + H]^+ = 521.07< / annotation>< / semantics>, Found = 521.21. Example 9: preparation of compound 88 Step 1: preparation of compound 88 [Image disponible dans le document PDF, Image available in the PDF document] 145.14 mg of 2-(methylthio)ethanol and 199.21 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 3 mL of dichloromethane solution of the intermediate 54-3 (0.60 g) described in Example 5 was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 545 mg of colorless oil as compound 88. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.15 (d, <semantics>J=7.8<annotation encoding="application / x-tex">J = 7.8< / annotation>< / semantics> Hz, 1H), 7.94 (d, <semantics>J=9.6<annotation encoding="application / x-tex">J = 9.6< / annotation>< / semantics> Hz, 1H), 6.63 (d, <semantics>J=2.9<annotation encoding="application / x-tex">J = 2.9< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> H <semantics>=7.0,2.0 Hz,1H,4.39−4.21 (m, 2H),3.42 (s, 3H),2.83−2.66 (m, 2H),2.11−2.07<annotation encoding="application / x-tex">= 7.0, 2.0 \text{ Hz}, 1\text{H}, 4.39 - 4.21 \text{ (m, 2H)}, 3.42 \text{ (s, 3H)}, 2.83 - 2.66 \text{ (m, 2H)}, 2.11 - 2.07< / annotation>< / semantics> (m, 3H), 1.55 (d, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=512.04<annotation encoding="application / x-tex">[M + H]^+ = 512.04< / annotation>< / semantics>, Found = 512.54. Example 10: preparation of compound 92 Step 1: preparation of compound 92 [Image disponible dans le document PDF, Image available in the PDF document] 250.0 mg of compound 88 and 10 mL of dichloromethane were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 84.11 mg of m-chloroperoxybenzoic acid was added, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 177 mg of colorless oil as compound 92. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.22 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 8.01 (d, <semantics>J=9.6<annotation encoding="application / x-tex">J = 9.6< / annotation>< / semantics> Hz, 1H), 6.70 <semantics>(d,J=2.9 Hz,1H),5.45−5.35 (m, 1H),4.66−4.42 (m, 2H),3.49 (s, 3H),3.29−<annotation encoding="application / x-tex">(d, J = 2.9 \text{ Hz}, 1\text{H}), 5.45 - 5.35 \text{ (m, 1H)}, 4.66 - 4.42 \text{ (m, 2H)}, 3.49 \text{ (s, 3H)}, 3.29 -< / annotation>< / semantics> 3.02 (m, 2H), 2.73 – 2.62 (m, 3H), 1.61 (d, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 3H). LCMS (ESI) [M + H]+ =529.04, Found =528.65. Example 11: preparation of compound 93 Step 1: preparation of compound 93 [Image disponible dans le document PDF, Image available in the PDF document] 97.77 mg of 2-methylsulfonyl ethanol and 99.61 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 2 mL of dichloromethane solution of the intermediate 54-3 (0.30 g) described in Example 5 was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 192 mg of compound 93. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.16 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 7.94 (d, <semantics>J=9.5<annotation encoding="application / x-tex">J = 9.5< / annotation>< / semantics> Hz, 1H), 6.63 (d, <semantics>J=3.2<annotation encoding="application / x-tex">J = 3.2< / annotation>< / semantics> Hz, 1H), 5.44 – 5.28 (m, 1H), 4.57 – 4.41 (m, 2H), 3.55 (t, <semantics>J=5.8<annotation encoding="application / x-tex">J = 5.8< / annotation>< / semantics> Hz, 2H), 3.02 (s, 3H), 1.54 (d, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=545.03<annotation encoding="application / x-tex">[M + H]^+ = 545.03< / annotation>< / semantics>, Found = 544.58. Example 12: preparation of compound 96 [Image disponible dans le document PDF, Image available in the PDF document] 0.5 g of the intermediate 53-3 described in Example 5, 5 mL of dichloromethane, 97.2 mg of (S)-glycidol, and 0.17 g of triethylamine were added to a 25 mL single-necked flask, and stirred overnight at room temperature. After the reaction was completed, 5 mL of water was added, the solution was stirred and separated to obtain an organic phase, the organic phase was dried with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. Column chromatography purification was carried out to obtain 215 mg of compound 96. 1H NMR (400 MHz, CDCl3) δ 7.97 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 7.40 (d, <semantics>J=9.1<annotation encoding="application / x-tex">J = 9.1< / annotation>< / semantics> Hz, 1H), 6.38 (d, <semantics>J=1.1<annotation encoding="application / x-tex">J = 1.1< / annotation>< / semantics> Hz, 1H), 5.37 (q, <semantics>J=1.1<annotation encoding="application / x-tex">J = 1.1< / annotation>< / semantics> Hz, 1H), 5.37 (q, <semantics>J=1.1<annotation encoding="application / x-tex">J = 1.1< / annotation>< / semantics> Hz, 1H), 5.37 (q, <semantics>J=1.1<annotation encoding="application / x-tex">J = 1.1< / annotation>< / semantics> Hz, 1H), 5.37 (q, <semantics>J=1.1<annotation encoding="application / x-tex">J = 1.1< / annotation>< / semantics> Hz, 1H), 6.38 (d, <semantics>J=1.1<annotation encoding="application / x-tex">J = 1.1< / annotation>< / semantics> Hz, 1H <semantics>=7.0 Hz,1H,4.49 (dd,J=12.2,3.0 Hz,1H),4.07−3.94 (m, 1H),3.57 (s, 3H),3.22<annotation encoding="application / x-tex">= 7.0 \text{ Hz}, 1\text{H}, 4.49 \text{ (dd}, J = 12.2, 3.0 \text{ Hz}, 1\text{H}), 4.07 - 3.94 \text{ (m, 1H)}, 3.57 \text{ (s, 3H)}, 3.22< / annotation>< / semantics> <semantics>(tt,J=9.8,4.9 Hz,1H),2.84(q,J=4.4 Hz,1H),2.63(dd,J=4.7,2.6 Hz,1H),1.62<annotation encoding="application / x-tex">(tt, J = 9.8, 4.9 \text{ Hz}, 1\text{H}), 2.84 (q, J = 4.4 \text{ Hz}, 1\text{H}), 2.63 (dd, J = 4.7, 2.6 \text{ Hz}, 1\text{H}), 1.62< / annotation>< / semantics> <semantics>(t,J=9.2 Hz,3H)<annotation encoding="application / x-tex">(t, J = 9.2 \text{ Hz}, 3\text{H})< / annotation>< / semantics>. LCMS (ESI) <semantics>[M+H]+=495.05<annotation encoding="application / x-tex">[M + H]^+ = 495.05< / annotation>< / semantics>, Found = 495.05. Example 13: preparation of compound 97 [Image disponible dans le document PDF, Image available in the PDF document] 0.5 g of the intermediate 53-3 described in Example 5, 5 mL of dichloromethane, 97.2 mg of (R)-glycidol, and 0.17 g of triethylamine were added to a 25 mL single-necked flask, and stirred overnight at room temperature. After the reaction was completed, 5 mL of water was added, the solution was stirred and separated to obtain an organic phase, the organic phase was dried with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. Column chromatography purification was carried out to obtain 330 mg of compound 97. 1H NMR (400 MHz, CDCl3) δ 7.97 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 7.40 (d, <semantics>J=9.2<annotation encoding="application / x-tex">J = 9.2< / annotation>< / semantics> Hz, 1H), 6.37 (d, <semantics>J=2.3<annotation encoding="application / x-tex">J = 2.3< / annotation>< / semantics> Hz, 1H), 5.37 (qd, <semantics>J=3.4<annotation encoding="application / x-tex">J = 3.4< / annotation>< / semantics> <semantics>=7.1,2.2 Hz,1H),4.49 (dd,J=12.2,2.2 Hz,1H),4.13−3.98 (m, 1H),3.57 (d, J=1.1,2.2 Hz)<annotation encoding="application / x-tex">= 7.1, 2.2 \text{ Hz}, 1\text{H}), 4.49 \text{ (dd}, J = 12.2, 2.2 \text{ Hz}, 1\text{H}), 4.13 - 3.98 \text{ (m, 1H)}, 3.57 \text{ (d, } J = 1.1, 2.2 \text{ Hz})< / annotation>< / semantics> 2.0 Hz, 3H), 3.20 (tt, <semantics>J=5.7<annotation encoding="application / x-tex">J = 5.7< / annotation>< / semantics>, 2.8 Hz, 1H), 2.84 (t, <semantics>J=4.5<annotation encoding="application / x-tex">J = 4.5< / annotation>< / semantics> Hz, 1H), 2.67 (dt, <semantics>J=10.9<annotation encoding="application / x-tex">J = 10.9< / annotation>< / semantics>, 5.6 Hz, 1H), 1.63 (d, <semantics>J=7.1<annotation encoding="application / x-tex">J = 7.1< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=495.05<annotation encoding="application / x-tex">[M + H]^+ = 495.05< / annotation>< / semantics>, Found <semantics>=495.30.<annotation encoding="application / x-tex">=495.30.< / annotation>< / semantics> Example 14: preparation of intermediate 105-3 Step 1: preparation of intermediate 105-1 [Image disponible dans le document PDF, Image available in the PDF document] 324.4 mg of methyl L-lactate was added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, and the intermediate 1-8 (1 g) described in Example 1 was added dropwise, followed by 394 mg of triethylamine. Then, a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 923 mg of intermediate 105-1. Step 2: preparation of intermediate 105-2 [Image disponible dans le document PDF, Image available in the PDF document] 923 mg of intermediate 105-1, 6.46 g of hydrochloric acid (36%), and 6.46 g of acetic acid were added to a reaction flask and refluxed for 40 min, and the reaction solution was spun off to obtain 900 mg of intermediate 105-2. Step 3: preparation of intermediate 105-3 [Image disponible dans le document PDF, Image available in the PDF document] 900 mg of intermediate 105-2, 366.49 mg of dichlorosulfoxide, 2 drops of DMF, and 4.5 g of 1,2-dichloroethane were added to a reaction flask, a reflux reaction occurred for 3 h, and the reaction solution was spun off to obtain 800 mg of intermediate 105-3. Example 15: preparation of compound 105 [Image disponible dans le document PDF, Image available in the PDF document] 0.6 g of the intermediate 105-3 described in Example 14, 0.120 g of 2-methoxyethanol, 10 g of dichloromethane, and 0.2 g of triethylamine were added to a reaction flask, blown with nitrogen, and stirred at room temperature for 1 h until the reaction ended. After the reaction was completed, column chromatography purification was carried out to obtain 0.40 g of compound 105. 1H NMR (400 MHz, CDCl3) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (dd, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics>, 2.0 Hz, 1H), 7.40 (d, <semantics>J=9.2<annotation encoding="application / x-tex">J = 9.2< / annotation>< / semantics> Hz, 1H), 6.37 (s, 1H), 5.36 (q, <semantics>J=7.0 Hz<annotation encoding="application / x-tex">J = 7.0 \text{ Hz}< / annotation>< / semantics>, 1H), 4.32 (s, 2H), 3.60 (t, <semantics>J=4.6 Hz<annotation encoding="application / x-tex">J = 4.6 \text{ Hz}< / annotation>< / semantics>, 2H), 3.57 (s, 3H), 3.36 (s, 3H), 1.62 <semantics>(d,J=7.0 Hz,3H)<annotation encoding="application / x-tex">(d, J = 7.0 \text{ Hz}, 3\text{H})< / annotation>< / semantics>. LCMS (ESI) <semantics>[M+H]+=497.07<annotation encoding="application / x-tex">[M + H]^+ = 497.07< / annotation>< / semantics>, Found = 497.34. Example 16: preparation of compound 112 [Image disponible dans le document PDF, Image available in the PDF document] The intermediate 105-3 (1 g) described in Example 14 was weighed into a 25 ml single-necked flask, and 10 mL of dichloromethane, 268 mg of 2-allyloxyethanol, and 330 mg of triethylamine were added, followed by stirring at room temperature for reaction. After 15 h, the reaction ended upon LCMS test. 5 mL of water was added, and the solution was stirred and separated to obtain an organic phase. The organic phase was dried, and the excess solvent was evaporated under reduced pressure. After column chromatography purification (PE: EA=4:1), 768 mg of colorless oily liquid was obtained as compound 112. 1H NMR (400 MHz, CDCl3) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (dd, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics>, 1.9 Hz, 1H), 7.40 (d, <semantics>J=9.2<annotation encoding="application / x-tex">J = 9.2< / annotation>< / semantics> Hz, 1H), 6.37 (s, 1H), 5.87 (ddd, <semantics>J=22.7<annotation encoding="application / x-tex">J = 22.7< / annotation>< / semantics>, 10.7, 5.6 Hz, 1H), 5.35 (t, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 1H), 5.27 (dd, <semantics>J=17.2<annotation encoding="application / x-tex">J = 17.2< / annotation>< / semantics>, 1.5 Hz, 1H), 5.18 (d, <semantics>J=10.4<annotation encoding="application / x-tex">J = 10.4< / annotation>< / semantics> Hz, 1H), <semantics>4.43−4.24<annotation encoding="application / x-tex">4.43 - 4.24< / annotation>< / semantics> (m, 2H), <semantics>4.00<annotation encoding="application / x-tex">4.00< / annotation>< / semantics> (d, <semantics>J=5.4<annotation encoding="application / x-tex">J = 5.4< / annotation>< / semantics> Hz, 2H), <semantics>3.65<annotation encoding="application / x-tex">3.65< / annotation>< / semantics> (t, <semantics>J=4.8<annotation encoding="application / x-tex">J = 4.8< / annotation>< / semantics> Hz, 2H), <semantics>3.57<annotation encoding="application / x-tex">3.57< / annotation>< / semantics> (s, 3H), 1.62 (d, <semantics>J=7.1<annotation encoding="application / x-tex">J = 7.1< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=523.08<annotation encoding="application / x-tex">[M + H]^+ = 523.08< / annotation>< / semantics>, Found = 523.10. Example 17: preparation of compound 130 [Image disponible dans le document PDF, Image available in the PDF document] 1 g of the intermediate 105-3 described in Example 14 was dissolved in 5 mL of 1,2-dichloroethane, a 1,2-dichloroethane solution of propynol ethoxylate (220 mg) was added dropwise, the solution was stirred at 20°C for 10 minutes, and then 330 mg of triethylamine was added dropwise. After the reaction of the raw materials was completed upon LCMS test, 20 mL of hydrochloric acid (1N) was added for washing, the solution was separated, the organic phase was dried with anhydrous sodium sulfate, and column chromatography purification was carried out to obtain 230 mg of colorless oily liquid as compound 130. 1H NMR (400 MHz, Chloroform-d) δ 7.97 (dd, <semantics>J=7.7,2.1 Hz,1H),7.40(d,J=9.2 Hz,1H),6.38(d,J=1.0 Hz,1H),5.36(q,J=7.1)<annotation encoding="application / x-tex">J = 7.7, 2.1 \text{ Hz}, 1H), 7.40 (d, J = 9.2 \text{ Hz}, 1H), 6.38 (d, J = 1.0 \text{ Hz}, 1H), 5.36 (q, J = 7.1)< / annotation>< / semantics> Hz, 1H), 5.30 (s, 1H), 4.17 (dd, <semantics>J=2.4<annotation encoding="application / x-tex">J = 2.4< / annotation>< / semantics>, 0.7 Hz, 2H), 3.76 (dt, <semantics>J=6.9<annotation encoding="application / x-tex">J = 6.9< / annotation>< / semantics>, 3.0 Hz, 2H), <semantics>3.59−3.55<annotation encoding="application / x-tex">3.59 - 3.55< / annotation>< / semantics> (m, 3H), <semantics>1.62<annotation encoding="application / x-tex">1.62< / annotation>< / semantics> (dd, <semantics>J=7.1<annotation encoding="application / x-tex">J = 7.1< / annotation>< / semantics>, <semantics>1.0<annotation encoding="application / x-tex">1.0< / annotation>< / semantics> Hz, 3H), <semantics>1.33−1.23<annotation encoding="application / x-tex">1.33 - 1.23< / annotation>< / semantics> (m, 2H). LCMS (ESI) <semantics>[M+H]+=521.07<annotation encoding="application / x-tex">[M + H]^+ = 521.07< / annotation>< / semantics>, Found = 521.12. Example 18: preparation of compound 139 Step 1: preparation of compound 139 [Image disponible dans le document PDF, Image available in the PDF document] 145.14 mg of 2-(methylthio)ethanol and 199.21 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 3 mL of dichloromethane solution of the intermediate 105-3 (0.60 g) described in Example 14 was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 419 mg of colorless oil as compound 139. <semantics>1<annotation encoding="application / x-tex">^{1}< / annotation>< / semantics>H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.15 (d, <semantics>J=7.8<annotation encoding="application / x-tex">J = 7.8< / annotation>< / semantics> Hz, 1H), 7.94 (d, <semantics>J=9.6<annotation encoding="application / x-tex">J = 9.6< / annotation>< / semantics> Hz, 1H), 6.63 (d, <semantics>J=2.9<annotation encoding="application / x-tex">J = 2.9< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz, 1H), 5.32 (dd, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz, 1H), 6.63 (d, <semantics>J=3.6<annotation encoding="application / x-tex">J = 3.6< / annotation>< / semantics> Hz <semantics>=7.0,2.0 Hz,1H),4.39−4.21 (m, 2H),3.42 (s, 3H),2.83−2.66 (m, 2H),2.11−2.07<annotation encoding="application / x-tex">= 7.0, 2.0 \text{ Hz}, 1\text{H}), 4.39 - 4.21 \text{ (m, 2H)}, 3.42 \text{ (s, 3H)}, 2.83 - 2.66 \text{ (m, 2H)}, 2.11 - 2.07< / annotation>< / semantics> (m, 3H), 1.55 (d, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=512.04<annotation encoding="application / x-tex">[M + H]^+ = 512.04< / annotation>< / semantics>, Found = 512.54. Example 19: preparation of compound 143 Step 1: preparation of compound 143 [Image disponible dans le document PDF, Image available in the PDF document] 250.0 mg of the compound 139 described in Example 18 and 10 mL of dichloromethane were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 84.11 mg of m-chloroperoxybenzoic acid was added, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 170 mg of colorless oil as compound 143. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.21 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 8.01 (d, <semantics>J=9.6 Hz<annotation encoding="application / x-tex">J = 9.6 \text{ Hz}< / annotation>< / semantics>, 1H), 6.70 (d, <semantics>J=2.8 Hz<annotation encoding="application / x-tex">J = 2.8 \text{ Hz}< / annotation>< / semantics>, 1H), 5.41 (qt, <semantics>J=7.2<annotation encoding="application / x-tex">J = 7.2< / annotation>< / semantics>, 1.6 Hz, 1H), 4.70 – 4.43 (m, 2H), 3.48 (s, 3H), <semantics>3.27−3.00<annotation encoding="application / x-tex">3.27 - 3.00< / annotation>< / semantics> (m, 2H), <semantics>2.65<annotation encoding="application / x-tex">2.65< / annotation>< / semantics> (d, <semantics>J=2.6<annotation encoding="application / x-tex">J = 2.6< / annotation>< / semantics> Hz, 3H), <semantics>1.61<annotation encoding="application / x-tex">1.61< / annotation>< / semantics> (d, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=529.04<annotation encoding="application / x-tex">[M + H]^+ = 529.04< / annotation>< / semantics>, Found = 528.65. Example 20: preparation of compound 144 Step 1: preparation of compound 144 [Image disponible dans le document PDF, Image available in the PDF document] 97.77 mg of 2-methylsulfonyl ethanol and 99.61 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 2 mL of dichloromethane solution of the intermediate 105-3 (0.30 g) described in Example 14 was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 166 mg of compound 144. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.16 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics>) Hz, 1H), 7.94 (d, <semantics>J=9.5<annotation encoding="application / x-tex">J = 9.5< / annotation>< / semantics> Hz, 1H), 6.63 (d, <semantics>J=3.2<annotation encoding="application / x-tex">J = 3.2< / annotation>< / semantics> Hz, 1H), 5.43 – 5.32 (m, 1H), 4.57 <semantics>−4.41<annotation encoding="application / x-tex">-4.41< / annotation>< / semantics> (m, 2H), 3.55 (t, <semantics>J=5.8<annotation encoding="application / x-tex">J = 5.8< / annotation>< / semantics> Hz, 2H), 3.02 (s, 3H), 1.54 (d, <semantics>J=7.2<annotation encoding="application / x-tex">J = 7.2< / annotation>< / semantics> Hz, 3H). LCMS <semantics>(ESI)[M+H]+=545.03<annotation encoding="application / x-tex">(ESI) [M + H]^{+} = 545.03< / annotation>< / semantics>, Found = 544.58. Example 21: preparation of compound 147 [Image disponible dans le document PDF, Image available in the PDF document] 0.5 g of the intermediate 105-3 described in Example 14, 5 mL of dichloromethane, 97.2 mg of (S)-glycidol, and 0.17 g of triethylamine were added to a 25 mL single-necked flask, and stirred overnight at room temperature. After the reaction was completed, 5 mL of water was added, the solution was stirred and separated to obtain an organic phase, the organic phase was dried with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. Column chromatography purification was carried out to obtain 215 mg of compound 147. 1H NMR (400 MHz, CDCl3) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 7.40 (d, <semantics>J=9.1<annotation encoding="application / x-tex">J = 9.1< / annotation>< / semantics> Hz, 1H), 6.38 (d, <semantics>J=1.1 Hz<annotation encoding="application / x-tex">J = 1.1 \text{ Hz}< / annotation>< / semantics>, 1H), 5.37 (q, <semantics>J=7.0 Hz<annotation encoding="application / x-tex">J = 7.0 \text{ Hz}< / annotation>< / semantics>, 1H), 4.49 (dd, <semantics>J=12.2<annotation encoding="application / x-tex">J = 12.2< / annotation>< / semantics>, 3.0 Hz, 1H), 4.07 – 3.94 (m, 1H), 3.57 (s, 3H), 3.22 (tt, <semantics>J=9.8<annotation encoding="application / x-tex">J = 9.8< / annotation>< / semantics>, 4.9 Hz, 1H), 2.84 (q, <semantics>J=4.4<annotation encoding="application / x-tex">J = 4.4< / annotation>< / semantics> Hz, 1H), 2.63 (dd, <semantics>J=4.7,2.6 Hz,1H<annotation encoding="application / x-tex">J = 4.7, 2.6 \text{ Hz}, 1\text{H}< / annotation>< / semantics>), 1.62 (t, <semantics>J=9.2 Hz,3H<annotation encoding="application / x-tex">J = 9.2 \text{ Hz}, 3\text{H}< / annotation>< / semantics>). LCMS (ESI) [M + H]+ =495.05, Found =495.12. Example 22: preparation of compound 148 [Image disponible dans le document PDF, Image available in the PDF document] 0.5 g of the intermediate 105-3 described in Example 14, 5 mL of dichloromethane, 97.2 mg of (R)-glycidol, and 0.17 g of triethylamine were added to a 25 mL single-necked flask, and stirred overnight at room temperature. After the reaction was completed, 5 mL of water was added, the solution was stirred and separated to obtain an organic phase, the organic phase was dried with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. Column chromatography purification was carried out to obtain 240 mg of compound 148. 1H NMR (400 MHz, CDCl3) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 7.40 (d, <semantics>J=9.1<annotation encoding="application / x-tex">J = 9.1< / annotation>< / semantics> Hz, 1H), 6.37 (d, <semantics>J=2.2 Hz<annotation encoding="application / x-tex">J = 2.2 \text{ Hz}< / annotation>< / semantics>, 1H), 5.37 (dd, <semantics>J=7.1<annotation encoding="application / x-tex">J = 7.1< / annotation>< / semantics>, 2.1 Hz, 1H), 4.49 (dd, <semantics>J=12.2<annotation encoding="application / x-tex">J = 12.2< / annotation>< / semantics>, 2.3 Hz, 1H), 4.07 <semantics>(ddd,J=12.2,5.9,2.0 Hz,1H),3.57(d,J=1.9 Hz,3H),3.20(tt,J=5.8,2.8 Hz,1H),<annotation encoding="application / x-tex">(ddd, J = 12.2, 5.9, 2.0 \text{ Hz}, 1\text{H}), 3.57 (d, J = 1.9 \text{ Hz}, 3\text{H}), 3.20 (tt, J = 5.8, 2.8 \text{ Hz}, 1\text{H}),< / annotation>< / semantics> 2.83 (t, <semantics>J=4.5<annotation encoding="application / x-tex">J = 4.5< / annotation>< / semantics> Hz, 1H), 2.72 – 2.62 (m, 1H), 1.63 (d, <semantics>J=7.1<annotation encoding="application / x-tex">J = 7.1< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=495.05<annotation encoding="application / x-tex">[M + H]^+ = 495.05< / annotation>< / semantics>, Found = 495.06. Example 23: preparation of intermediate 156-3 Step 1: preparation of intermediate 156-1 [Image disponible dans le document PDF, Image available in the PDF document] 20.0 g of the intermediate 1-8 described in Example 1, 4.86 g of methyl lactate, and 100 g of dichloromethane were added to a reaction flask, blown with nitrogen, and stirred at room temperature. 5.9 g of triethylamine was added dropwise within 60 min, followed by stirring overnight at room temperature. After the reaction was completed, column chromatography purification was carried out to obtain 15.8 g of intermediate 156-1. Step 2: preparation of intermediate 156-2 [Image disponible dans le document PDF, Image available in the PDF document] 15.0 g of intermediate 22-1, 90 g of hydrochloric acid (36%), and 90 g of acetic acid were added into a reaction flask and stirred at 60°C for 40 min until the reaction ended, and the solvent was spun off to obtain 13.7 g of intermediate 156-2. Step 3: preparation of intermediate 156-3 [Image disponible dans le document PDF, Image available in the PDF document] 900 mg of intermediate 156-2, 366.49 mg of dichlorosulfoxide, 2 drops of DMF, and 4.5 g of 1,2-dichloroethane were added to a reaction flask, a reflux reaction occurred for 3 h, and the reaction solution was spun off to obtain 820 mg of intermediate 156-3. Example 24: preparation of compound 156 [Image disponible dans le document PDF, Image available in the PDF document] 0.6 g of the intermediate 156-3 described in Example 23, 0.120 g of 2-methoxyethanol, 10 g of dichloromethane, and 0.2 g of triethylamine were added to a reaction flask, blown with nitrogen, and stirred at room temperature for 1 h until the reaction ended. After the reaction was completed, column chromatography purification was carried out to obtain 0.395 g of compound 156. 1H NMR (400 MHz, CDCl3) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (dd, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics>, 2.0 Hz, 1H), 7.40 (d, <semantics>J=9.2<annotation encoding="application / x-tex">J = 9.2< / annotation>< / semantics> Hz, 1H), 6.37 (s, 1H), 5.36 (q, <semantics>J=7.0 Hz<annotation encoding="application / x-tex">J = 7.0 \text{ Hz}< / annotation>< / semantics>, 1H), 4.32 (s, 2H), 3.60 (t, <semantics>J=4.6 Hz<annotation encoding="application / x-tex">J = 4.6 \text{ Hz}< / annotation>< / semantics>, 2H), 3.57 (s, 3H), 3.36 (s,, 3H), 1.62 <semantics>(d,J=7.0 Hz,3H)<annotation encoding="application / x-tex">(d, J = 7.0 \text{ Hz}, 3\text{H})< / annotation>< / semantics>. LCMS (ESI) <semantics>[M+H]+=497.07<annotation encoding="application / x-tex">[M + H]^+ = 497.07< / annotation>< / semantics>, Found = 497.30. Example 25: preparation of compound 163 [Image disponible dans le document PDF, Image available in the PDF document] With reference to the methods of Examples 7 and 16, compound 163 was prepared by using the intermediate 156-3 described in Example 23 and 2-allyloxyethanol. Example 26: preparation of compound 181 [Image disponible dans le document PDF, Image available in the PDF document] With reference to the methods of Examples 8 and 17, compound 181 was prepared by using the intermediate 156-3 described in Example 23 and propynol ethoxylate. 1H NMR (400 MHz, Chloroform-d) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (dd, <semantics>J=7.7,2.1<annotation encoding="application / x-tex">J = 7.7, 2.1< / annotation>< / semantics> Hz, 1H), 7.40 <semantics>(d,J=9.2 Hz,1H),6.38(d,J=1.0 Hz,1H),5.36(q,J=7.1 Hz,1H),5.30(s,1H),<annotation encoding="application / x-tex">(d, J = 9.2 \text{ Hz}, 1\text{H}), 6.38 (d, J = 1.0 \text{ Hz}, 1\text{H}), 5.36 (q, J = 7.1 \text{ Hz}, 1\text{H}), 5.30 (s, 1\text{H}),< / annotation>< / semantics> <semantics>4.17 (dd, J=2.4,0.7 Hz, 2H),3.76 (dt, J=6.9,3.0 Hz, 2H),3.59−3.55 (m, 3H),1.62<annotation encoding="application / x-tex">4.17 \text{ (dd, } J = 2.4, 0.7 \text{ Hz, 2H)}, 3.76 \text{ (dt, } J = 6.9, 3.0 \text{ Hz, 2H)}, 3.59 - 3.55 \text{ (m, 3H)}, 1.62< / annotation>< / semantics> <semantics>(dd,J=7.1,1.0 Hz,3H),1.33−1.23 (m, 2H).LCMS(ESI)[M+H]+=521.07,<annotation encoding="application / x-tex">(dd, J = 7.1, 1.0 \text{ Hz}, 3H), 1.33 - 1.23 \text{ (m, 2H)}. LCMS (ESI) [M + H]^+ = 521.07,< / annotation>< / semantics> Found =521.11. Example 27: preparation of compound 190 Step 1: preparation of compound 190 [Image disponible dans le document PDF, Image available in the PDF document] 145.14 mg of 2-(methylthio)ethanol and 199.21 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 3 mL of dichloromethane solution of the intermediate 156-3 (0.60 g) described in Example 23 was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 409 mg of colorless oil as compound 190. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> <semantics>8.15 (d, J=7.8 Hz, 1H),7.94 (d, J=9.6 Hz, 1H),6.63 (d, J=2.9 Hz, 1H),5.32 (dd, J=2.9 Hz, 1H)<annotation encoding="application / x-tex">8.15 \text{ (d, } J = 7.8 \text{ Hz, } 1\text{H)}, 7.94 \text{ (d, } J = 9.6 \text{ Hz, } 1\text{H)}, 6.63 \text{ (d, } J = 2.9 \text{ Hz, } 1\text{H)}, 5.32 \text{ (dd, } J = 2.9 \text{ Hz, } 1\text{H)}< / annotation>< / semantics> <semantics>=7.0,2.0 Hz,1H),4.39−4.21 (m, 2H),3.42 (s, 3H),2.83−2.66 (m, 2H),2.11−2.07<annotation encoding="application / x-tex">= 7.0, 2.0 \text{ Hz}, 1\text{H}), 4.39 - 4.21 \text{ (m, 2H)}, 3.42 \text{ (s, 3H)}, 2.83 - 2.66 \text{ (m, 2H)}, 2.11 - 2.07< / annotation>< / semantics> (m, 3H), 1.55 (d, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=512.04<annotation encoding="application / x-tex">[M + H]^+ = 512.04< / annotation>< / semantics>, Found = 512.54. Example 28: preparation of compound 194 Step 1: preparation of compound 194 [Image disponible dans le document PDF, Image available in the PDF document] 250.0 mg of compound 190 and 10 mL of dichloromethane were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 84.11 mg of m-chloroperoxybenzoic acid was added, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 166 mg of colorless oil as compound 194. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.21 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 8.01 (d, <semantics>J=9.6<annotation encoding="application / x-tex">J = 9.6< / annotation>< / semantics> Hz, 1H), 6.70 <semantics>(d,J=2.8 Hz,1H),5.41 (qt, J=7.2,1.6 Hz,1H),4.70−4.43 (m, 2H),3.48 (s, 3H),<annotation encoding="application / x-tex">(d, J = 2.8 \text{ Hz}, 1\text{H}), 5.41 \text{ (qt, } J = 7.2, 1.6 \text{ Hz}, 1\text{H}), 4.70 - 4.43 \text{ (m, 2H)}, 3.48 \text{ (s, 3H)},< / annotation>< / semantics> <semantics>3.27−3.00<annotation encoding="application / x-tex">3.27 - 3.00< / annotation>< / semantics> (m, 2H), <semantics>2.65<annotation encoding="application / x-tex">2.65< / annotation>< / semantics> (d, <semantics>J=2.6<annotation encoding="application / x-tex">J = 2.6< / annotation>< / semantics> Hz, 3H), <semantics>1.61<annotation encoding="application / x-tex">1.61< / annotation>< / semantics> (d, <semantics>J=7.0<annotation encoding="application / x-tex">J = 7.0< / annotation>< / semantics> Hz, 3H). LCMS (ESI) <semantics>[M+H]+=529.04<annotation encoding="application / x-tex">[M + H]^+ = 529.04< / annotation>< / semantics>, Found = 528.65. Example 29: preparation of compound 195 Step 1: preparation of compound 195 [Image disponible dans le document PDF, Image available in the PDF document] 97.77 mg of 2-methylsulfonyl ethanol and 99.61 mg of triethylamine were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 2 mL of dichloromethane solution of the intermediate 156-3 (0.30 g) described in Example 23 was added dropwise, and then a reaction occurred at room temperature for 2 h. After the reaction was completed, column chromatography purification was carried out to obtain 168 mg of compound 195. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.16 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics>) Hz, 1H), 7.94 (d, <semantics>J=9.5<annotation encoding="application / x-tex">J = 9.5< / annotation>< / semantics> Hz, 1H), 6.63 (d, <semantics>J=3.2<annotation encoding="application / x-tex">J = 3.2< / annotation>< / semantics> Hz, 1H), 5.43 – 5.32 (m, 1H), 4.57 <semantics>−4.41<annotation encoding="application / x-tex">-4.41< / annotation>< / semantics> (m, 2H), 3.55 (t, <semantics>J=5.8<annotation encoding="application / x-tex">J = 5.8< / annotation>< / semantics> Hz, 2H), 3.02 (s, 3H), 1.54 (d, <semantics>J=7.2<annotation encoding="application / x-tex">J = 7.2< / annotation>< / semantics> Hz, 3H). LCMS <semantics>(ESI)[M+H]+=545.03<annotation encoding="application / x-tex">(ESI) [M + H]^{+} = 545.03< / annotation>< / semantics>, Found = 544.58. Example 30: preparation of compound 198 [Image disponible dans le document PDF, Image available in the PDF document] With reference to the methods of Examples 12 and 21, compound 198 was prepared by using the intermediate 156-3 described in Example 23 and (S)-glycidol. 1H NMR (400 MHz, CDCl3) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 7.40 (d, <semantics>J=9.1<annotation encoding="application / x-tex">J = 9.1< / annotation>< / semantics> Hz, 1H), 6.38 <semantics>(d,J=1.1 Hz,1H),5.37(q,J=7.0 Hz,1H),4.49(dd,J=12.2,3.0 Hz,1H),4.07−<annotation encoding="application / x-tex">(d, J = 1.1 \text{ Hz}, 1\text{H}), 5.37 (q, J = 7.0 \text{ Hz}, 1\text{H}), 4.49 (dd, J = 12.2, 3.0 \text{ Hz}, 1\text{H}), 4.07 -< / annotation>< / semantics> <semantics>3.94 (m, 1H),3.57 (s, 3H),3.22 (tt, J=9.8,4.9 Hz, 1H),2.84 (q, J=4.4 Hz, 1H),2.63<annotation encoding="application / x-tex">3.94 \text{ (m, 1H)}, 3.57 \text{ (s, 3H)}, 3.22 \text{ (tt, } J = 9.8, 4.9 \text{ Hz, 1H)}, 2.84 \text{ (q, } J = 4.4 \text{ Hz, 1H)}, 2.63< / annotation>< / semantics> <semantics>(dd,J=4.7,2.6 Hz,1H),1.62(t,J=9.2 Hz,3H). LCMS (ESI) [M+H]+=495.05,<annotation encoding="application / x-tex">(dd, J = 4.7, 2.6 \text{ Hz}, 1\text{H}), 1.62 (t, J = 9.2 \text{ Hz}, 3\text{H}). \text{ LCMS (ESI) } [\text{M} + \text{H}]^+ = 495.05,< / annotation>< / semantics> Found =495.04. Example 31: preparation of compound 199 [Image disponible dans le document PDF, Image available in the PDF document] With reference to the methods of Examples 13 and 22, compound 199 was prepared by using the intermediate 156-3 described in Example 23 and (R)-glycidol. 1H NMR (400 MHz, CDCl3) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.97 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 7.40 (d, <semantics>J=9.2<annotation encoding="application / x-tex">J = 9.2< / annotation>< / semantics> Hz, 1H), 6.37 <semantics>(d,J=2.3 Hz,1H),5.37 (qd,J=7.1,2.2 Hz,1H),4.49 (dd,J=12.2,2.2 Hz,1H),<annotation encoding="application / x-tex">(d, J = 2.3 \text{ Hz}, 1\text{H}), 5.37 \text{ (qd}, J = 7.1, 2.2 \text{ Hz}, 1\text{H}), 4.49 \text{ (dd}, J = 12.2, 2.2 \text{ Hz}, 1\text{H}),< / annotation>< / semantics> <semantics>4.13−3.98<annotation encoding="application / x-tex">4.13 - 3.98< / annotation>< / semantics> (m, 1H), <semantics>3.57<annotation encoding="application / x-tex">3.57< / annotation>< / semantics> (d, <semantics>J=2.0<annotation encoding="application / x-tex">J = 2.0< / annotation>< / semantics> Hz, 3H), <semantics>3.20<annotation encoding="application / x-tex">3.20< / annotation>< / semantics> (tt, <semantics>J=5.7<annotation encoding="application / x-tex">J = 5.7< / annotation>< / semantics>, <semantics>2.8<annotation encoding="application / x-tex">2.8< / annotation>< / semantics> Hz, 1H), <semantics>2.84<annotation encoding="application / x-tex">2.84< / annotation>< / semantics> (t, <semantics>J=5.7<annotation encoding="application / x-tex">J = 5.7< / annotation>< / semantics>) <semantics>=4.5 Hz,1H,2.67 (dt,J=10.9,5.6 Hz,1H),1.63 (d,J=7.1 Hz,3H).LCMS(ESI)<annotation encoding="application / x-tex">= 4.5 \text{ Hz}, 1\text{H}, 2.67 \text{ (dt}, J = 10.9, 5.6 \text{ Hz}, 1\text{H}), 1.63 \text{ (d}, J = 7.1 \text{ Hz}, 3\text{H}). LCMS (ESI)< / annotation>< / semantics> <semantics>[M+H]+=495.05<annotation encoding="application / x-tex">[M + H]^+ = 495.05< / annotation>< / semantics>, Found = 495.20. Example 32: preparation of compound 207 Step 1: preparation of intermediate 207-1 [Image disponible dans le document PDF, Image available in the PDF document] 2.36 g of methyl 2-hydroxyisobutyrate, 1.91 g of DMAP, and 50 g of dichloromethane were added to a reaction flask, blown with nitrogen, and stirred at room temperature. 5 g of the intermediate 1-8 described in Example 1 was added dropwise within 20 min, followed by stirring at room temperature for 1 h. After the reaction was completed, column chromatography purification was carried out to obtain 3.57 g of intermediate 207-1. Step 2: preparation of intermediate 207-2 [Image disponible dans le document PDF, Image available in the PDF document] 3.57 g of intermediate 207-1, 20 g of hydrochloric acid (36%), and 20 g of acetic acid were added into a reaction flask and stirred at 120°C for 2 h. After a reaction ended, the reaction solution was poured into 100 ml of ice water, extraction was carried out with EA, and the organic phase was spun off to obtain 2.78 g of intermediate 207-2. Step 3: preparation of compound 207-3 [Image disponible dans le document PDF, Image available in the PDF document] 2.78 g of intermediate 207-2,1.1 g of sulfoxide chloride, 30 g of 1,2-dichloroethane, and 2 drops of DMF were added into a reaction flask for reflux stirring at 90°C. After one hour of reaction, the solvent was spun off to obtain 3.2g of intermediate 207-3. Step 4: preparation of compound 207 [Image disponible dans le document PDF, Image available in the PDF document] 0.3 g of intermediate 207-3, 0.054 g of 2-methoxyethanol, 10 g of dichloromethane, and 0.089 g of triethylamine were added into a reaction flask, blown with nitrogen, and stirred at room temperature. After the reaction was completed, 5 mL of water was added, and the solution was stirred and separated to obtain an organic phase. The organic phase was dried, and the excess solvent was evaporated under reduced pressure. Column chromatography purification was carried out to obtain 120 mg of white solid as compound 207. 1H NMR (400 MHz, CDCl3) δ 7.86 (d, <semantics>J=7.7 Hz<annotation encoding="application / x-tex">J = 7.7 \text{ Hz}< / annotation>< / semantics>, 1H), 7.38 (d, <semantics>J=9.2 Hz<annotation encoding="application / x-tex">J = 9.2 \text{ Hz}< / annotation>< / semantics>, 1H), 6.38 (s, 1H), 4.50 – 4.18 (m, 2H), 3.59 (s, 2H), 3.57 (s, 3H), 3.32 (s, 3H), 1.69 (s, 6H). LCMS (ESI) <semantics>[M+H]+=511.08<annotation encoding="application / x-tex">[M + H]^+ = 511.08< / annotation>< / semantics>, Found <semantics>=511.12.<annotation encoding="application / x-tex">=511.12.< / annotation>< / semantics> Example 33: preparation of compound 214 Step 1: preparation of compound 214 [Image disponible dans le document PDF, Image available in the PDF document] 1.04 g of 2-allyloxyethanol, 1.24 g of DMAP, and 30 g of dichloromethane were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 20 mL of dichloromethane solution of the intermediate 207-3 (3.2 g) described in Example 32 was added dropwise, and then a reaction occurred at room temperature for 1 h. After the reaction was completed, column chromatography purification was carried out to obtain 600 mg of compound 214. 1H NMR (400 MHz, DMSO-d6) δ <semantics>8.07 (d, J=7.8 Hz, 1H),7.92 (d, J=9.6 Hz, 1H),6.63 (s, 1H),5.90−5.73 (m, 1H),<annotation encoding="application / x-tex">8.07 \text{ (d, } J = 7.8 \text{ Hz, } 1\text{H)}, 7.92 \text{ (d, } J = 9.6 \text{ Hz, } 1\text{H)}, 6.63 \text{ (s, } 1\text{H)}, 5.90 - 5.73 \text{ (m, } 1\text{H)},< / annotation>< / semantics> <semantics>5.25−5.08<annotation encoding="application / x-tex">5.25 - 5.08< / annotation>< / semantics> (m, 2H), <semantics>4.27−4.19<annotation encoding="application / x-tex">4.27 - 4.19< / annotation>< / semantics> (m, 2H), <semantics>3.91<annotation encoding="application / x-tex">3.91< / annotation>< / semantics> (dt, <semantics>J=5.3<annotation encoding="application / x-tex">J = 5.3< / annotation>< / semantics>, <semantics>1.6<annotation encoding="application / x-tex">1.6< / annotation>< / semantics> Hz, 2H), <semantics>3.59−3.55<annotation encoding="application / x-tex">3.59 - 3.55< / annotation>< / semantics> (m, 2H), 3.42 (d, <semantics>J=1.3<annotation encoding="application / x-tex">J = 1.3< / annotation>< / semantics> Hz, 3H), 1.63 (s, 6H).LCMS (ESI) <semantics>[M+H]+=537.10<annotation encoding="application / x-tex">[M + H]^+ = 537.10< / annotation>< / semantics>, Found <semantics>=536.98.<annotation encoding="application / x-tex">=536.98.< / annotation>< / semantics> Example 34: preparation of compound 249 [Image disponible dans le document PDF, Image available in the PDF document] 0.71 g of (S)-glycidol, 0.5 g of DMAP, 2 g of triethylamine, and 2 mL of dichloromethane were added to a reaction flask, cooled in an ice bath, and blown with nitrogen. 2.57 g of the intermediate 207-3 described in Example 32 was added dropwise to dissolve in 20 mL of dichloromethane solution, and a reaction occurred at room temperature for 3 h. After the reaction was completed, column chromatography purification was carried out to obtain 3 g of oily compound as compound 249. 1H NMR (400 MHz, Chloroform-d) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.87 (d, <semantics>J=7.6<annotation encoding="application / x-tex">J = 7.6< / annotation>< / semantics> Hz, 1H), 7.39 (d, <semantics>J=9.1<annotation encoding="application / x-tex">J = 9.1< / annotation>< / semantics> Hz, 1H), 6.38 (s, 1H), 4.45 (dd, <semantics>J=12.2<annotation encoding="application / x-tex">J = 12.2< / annotation>< / semantics>, 3.4 Hz, 1H), 4.04 (dd, <semantics>J=12.2<annotation encoding="application / x-tex">J = 12.2< / annotation>< / semantics>, 6.0 Hz, 1H), 3.57 (s, 3H), 3.21 (dq, <semantics>J=6.4<annotation encoding="application / x-tex">J = 6.4< / annotation>< / semantics>, 3.3 Hz, 1H), 2.83 (t, <semantics>J=4.5<annotation encoding="application / x-tex">J = 4.5< / annotation>< / semantics> Hz, 1H), 2.64 (dd, <semantics>J=4.9<annotation encoding="application / x-tex">J = 4.9< / annotation>< / semantics>, 2.6 Hz, 1H), 1.70 (s, 6H). LCMS (ESI) <semantics>[M+H]+=509.07<annotation encoding="application / x-tex">[M + H]^+ = 509.07< / annotation>< / semantics>, Found = 508.93. Example 35: preparation of compound 250 [Image disponible dans le document PDF, Image available in the PDF document] 0.71 g of (R)-glycidol, 0.5 g of DMAP, 2 g of triethylamine, and 2 mL of dichloromethane were added to a reaction flask, cooled in an ice bath, and blown with nitrogen. 20 mL of dichloromethane solution of 2.57 g of the intermediate 207-3 described in Example 32 was added dropwise, and a reaction occurred at room temperature for 3 h. After the reaction was completed, column chromatography purification was carried out to obtain 2.9 g of oily compound as compound 250. 1H NMR (400 MHz, Chloroform-d) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.87 (d, <semantics>J=7.7<annotation encoding="application / x-tex">J = 7.7< / annotation>< / semantics> Hz, 1H), 7.39 (d, <semantics>J=9.2<annotation encoding="application / x-tex">J = 9.2< / annotation>< / semantics> Hz, 1H), 6.38 (s, 1H), 4.44 (dd, <semantics>J=12.2<annotation encoding="application / x-tex">J = 12.2< / annotation>< / semantics>, 3.4 Hz, 1H), 4.04 (dd, <semantics>J=12.2<annotation encoding="application / x-tex">J = 12.2< / annotation>< / semantics>, 6.0 Hz, 1H), 3.56 (s, 3H), 3.20 (dq, <semantics>J=6.1<annotation encoding="application / x-tex">J = 6.1< / annotation>< / semantics>, 3.5 Hz, 1H), 2.82 (t, <semantics>J=4.5<annotation encoding="application / x-tex">J = 4.5< / annotation>< / semantics> Hz, 1H), 2.63 (dd, <semantics>J=4.8<annotation encoding="application / x-tex">J = 4.8< / annotation>< / semantics>, 2.6 Hz, 1H), 1.70 (s, 6H). LCMS (ESI) <semantics>[M+H]+=509.07<annotation encoding="application / x-tex">[M + H]^+ = 509.07< / annotation>< / semantics>, Found = 509.10. Example 36: preparation of compound 251 Step 1: preparation of compound 251 [Image disponible dans le document PDF, Image available in the PDF document] With reference to the methods of Examples 34 and 35, compound 251 was prepared by using the intermediate 207-3 described in Example 32 and glycidol. 1H NMR (400 MHz, Chloroform-d) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 7.87 (d, <semantics>J=7.6<annotation encoding="application / x-tex">J = 7.6< / annotation>< / semantics> Hz, 1H), 7.39 (d, <semantics>J=9.1<annotation encoding="application / x-tex">J = 9.1< / annotation>< / semantics> Hz, 1H), 6.38 (s, 1H), 4.45 (dd, <semantics>J=12.2<annotation encoding="application / x-tex">J = 12.2< / annotation>< / semantics>, 3.4 Hz, 1H), 4.04 (dd, <semantics>J=12.2<annotation encoding="application / x-tex">J = 12.2< / annotation>< / semantics>, 6.0 Hz, 1H), 3.57 (s, 3H), 3.21 (dq, <semantics>J=6.4<annotation encoding="application / x-tex">J = 6.4< / annotation>< / semantics>, 3.3 Hz, 1H), 2.83 (t, <semantics>J=4.5<annotation encoding="application / x-tex">J = 4.5< / annotation>< / semantics> Hz, 1H), 2.64 (dd, <semantics>J=4.9<annotation encoding="application / x-tex">J = 4.9< / annotation>< / semantics>, 2.6 Hz, 1H), 1.70 (s, 6H). LCMS (ESI) <semantics>[M+H]+=509.07<annotation encoding="application / x-tex">[M + H]^+ = 509.07< / annotation>< / semantics>, Found = 508.97. Example 37: preparation of compound 258 Step 1: preparation of compound 258-1 [Image disponible dans le document PDF, Image available in the PDF document] 0.6 g of methyl 1-hydroxy-1-cyclopropanecarboxylate, 0.57 g of DMAP, and 25 g of dichloromethane were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 10 mL of dichloromethane solution of the intermediate 1-8 (1.22 g) described in Example 1 was added dropwise, and then a reaction occurred at room temperature for 1 h. After the reaction was completed, column chromatography purification was carried out to obtain 1.1g of intermediate 258-1. Step 2: preparation of compound 258-2 [Image disponible dans le document PDF, Image available in the PDF document] 1.1 g of intermediate 258-1, 8 g of hydrochloric acid (36%), and 8 g of acetic acid were added into a reaction flask and stirred at 110°C for 4 h. After a reaction ended, the reaction solution was poured into 100 ml of ice water, extraction was carried out with EA, and the organic phase was spun off to obtain 1.06g of intermediate 258-2. Step 3: preparation of compound 258-3 [Image disponible dans le document PDF, Image available in the PDF document] 1.06 g of intermediate 258-2, 0.42 g of sulfoxide chloride, 20 g of 1,2-dichloroethane, and 2 drops of DMF were added into a reaction flask for reflux stirring at 90°C. After one hour of reaction, the solvent was spun off to obtain 1.1 g of intermediate 258-3. Step 4: preparation of compound 258 [Image disponible dans le document PDF, Image available in the PDF document] 0.211 g of 2-methoxyethanol, 0.323 g of triethylamine, and 15 g of dichloromethane were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 10 mL of dichloromethane solution of the intermediate 258-3 (1.0 g) was added dropwise, and then a reaction occurred at room temperature for 1 h. After the reaction was completed, column chromatography purification was carried out to obtain 201mg of compound 258. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.21 (d, <semantics>J=<annotation encoding="application / x-tex">J=< / annotation>< / semantics> 7.6 Hz, 1H), 8.01 (d, <semantics>J=9.4<annotation encoding="application / x-tex">J = 9.4< / annotation>< / semantics> Hz, 1H), 6.70 (s, 1H), 4.29 (t, <semantics>J=4.7<annotation encoding="application / x-tex">J = 4.7< / annotation>< / semantics> Hz, 2H), 3.57 (t, <semantics>J=4.7<annotation encoding="application / x-tex">J = 4.7< / annotation>< / semantics> Hz, 2H), 3.57 (t, <semantics>J=4.7<annotation encoding="application / x-tex">J = 4.7< / annotation>< / semantics> Hz, 2H), 3.57 (t, <semantics>J=4.7<annotation encoding="application / x-tex">J = 4.7< / annotation>< / semantics> Hz, 2H), 3.57 (t, <semantics>J=4.7<annotation encoding="application / x-tex">J = 4.7< / annotation>< / semantics> Hz, 2H), 3.57 (t, <semantics>J=4.7<annotation encoding="application / x-tex">J = 4.7< / annotation>< / semantics> Hz, 2H) <semantics>=4.6 Hz,2H,3.49 (s, 3H),3.29 (s, 3H),1.67−1.48 (m, 4H).LCMS (ESI)[M+H]+<annotation encoding="application / x-tex">= 4.6 \text{ Hz}, 2\text{H}, 3.49 \text{ (s, 3H)}, 3.29 \text{ (s, 3H)}, 1.67-1.48 \text{ (m, 4H)}.\text{LCMS (ESI)} [\text{M} + \text{H}]^{+}< / annotation>< / semantics> =509.07, Found =508.92. Example 38: preparation of compound 300 Step 1: preparation of compound 300 [Image disponible dans le document PDF, Image available in the PDF document] 0.308 g of (S)-glycidol, 0.485 g of triethylamine, and 20 g of dichloromethane were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 15 mL of dichloromethane solution of the intermediate 258-3 (1.5 g) described in Example 37 was added dropwise, and then a reaction occurred at room temperature for 1 h. After the reaction was completed, column chromatography purification was carried out to obtain 212mg of compound 300. 1H NMR (400 MHz, DMSO-d6) δ 8.22 <semantics>(d,J=7.8 Hz,1H),8.01(d,J=9.6 Hz,1H),6.69(s,1H),4.52(dd,J=12.3,2.6 Hz,<annotation encoding="application / x-tex">(d, J = 7.8 \text{ Hz}, 1\text{H}), 8.01 (d, J = 9.6 \text{ Hz}, 1\text{H}), 6.69 (s, 1\text{H}), 4.52 (dd, J = 12.3, 2.6 \text{ Hz},< / annotation>< / semantics> 1H), <semantics>4.03<annotation encoding="application / x-tex">4.03< / annotation>< / semantics> (dd, <semantics>J=12.3<annotation encoding="application / x-tex">J = 12.3< / annotation>< / semantics>, <semantics>6.3<annotation encoding="application / x-tex">6.3< / annotation>< / semantics> Hz, 1H), <semantics>3.51−3.45<annotation encoding="application / x-tex">3.51 - 3.45< / annotation>< / semantics> (m, 3H), <semantics>3.24<annotation encoding="application / x-tex">3.24< / annotation>< / semantics> (ddt, <semantics>J=6.7<annotation encoding="application / x-tex">J = 6.7< / annotation>< / semantics>, <semantics>4.2<annotation encoding="application / x-tex">4.2< / annotation>< / semantics>, <semantics>2.6<annotation encoding="application / x-tex">2.6< / annotation>< / semantics> Hz, 1H), 2.83 (dd, <semantics>J=5.0<annotation encoding="application / x-tex">J = 5.0< / annotation>< / semantics>, 4.2 Hz, 1H), 2.68 (dd, <semantics>J=5.0<annotation encoding="application / x-tex">J = 5.0< / annotation>< / semantics>, 2.6 Hz, 1H), 1.68 – 1.51 (m, 4H).LCMS (ESI) <semantics>[M+H]+=507.05<annotation encoding="application / x-tex">[M + H]^+ = 507.05< / annotation>< / semantics>, Found = 506.96. Example 39: preparation of compound 301 Step 1: preparation of compound 301 [Image disponible dans le document PDF, Image available in the PDF document] 0.205 g of (R)-glycidol, 0.323 g of triethylamine, and 15 g of dichloromethane were added to a reaction flask, cooled in an ice bath, stirred, and blown with nitrogen, 15 mL of dichloromethane solution of the intermediate 258-3 (1.0 g) descried in Example 37 was added dropwise, and then a reaction occurred at room temperature for 1 h. After the reaction was completed, column chromatography purification was carried out to obtain 222mg of compound 301. 1H NMR (400 MHz, DMSO-d6) δ 8.15 <semantics>(d,J=7.8 Hz,1H),7.94(d,J=9.6 Hz,1H),6.63(s,1H),4.46(dd,J=12.3,2.7 Hz,<annotation encoding="application / x-tex">(d, J = 7.8 \text{ Hz}, 1\text{H}), 7.94 (d, J = 9.6 \text{ Hz}, 1\text{H}), 6.63 (s, 1\text{H}), 4.46 (dd, J = 12.3, 2.7 \text{ Hz},< / annotation>< / semantics> 1H), 3.97 (dd, <semantics>J=12.3<annotation encoding="application / x-tex">J = 12.3< / annotation>< / semantics>, 6.2 Hz, 1H), 3.46 – 3.40 (m, 3H), 3.18 (ddt, <semantics>J=6.7<annotation encoding="application / x-tex">J = 6.7< / annotation>< / semantics>, 4.2, 2.6 Hz, 1H), 2.77 (dd, <semantics>J=5.0<annotation encoding="application / x-tex">J = 5.0< / annotation>< / semantics>, 4.3 Hz, 1H), 2.62 (dd, <semantics>J=5.0<annotation encoding="application / x-tex">J = 5.0< / annotation>< / semantics>, 2.6 Hz, 1H), 1.61 – 1.45 (m, 4H).LCMS (ESI) <semantics>[M+H]+=507.05<annotation encoding="application / x-tex">[M + H]^+ = 507.05< / annotation>< / semantics>, Found = 507.10. Example 40: preparation of compound 302 Step 1: preparation of compound 302 [Image disponible dans le document PDF, Image available in the PDF document] With reference to the methods of Examples 38 and 39, compound 302 was prepared by using the intermediate 258-3 described in Example 37 and glycidol. 1H NMR (400 MHz, DMSO-<semantics>d6<annotation encoding="application / x-tex">d_6< / annotation>< / semantics>) <semantics>δ<annotation encoding="application / x-tex">\delta< / annotation>< / semantics> 8.22 (d, <semantics>J=7.8<annotation encoding="application / x-tex">J = 7.8< / annotation>< / semantics> Hz, 1H), 8.01 (d, <semantics>J=9.6<annotation encoding="application / x-tex">J = 9.6< / annotation>< / semantics> Hz, 1H), 6.69 (s, 1H), 4.52 (dd, <semantics>J=12.3<annotation encoding="application / x-tex">J = 12.3< / annotation>< / semantics>, 2.6 Hz, 1H), 4.03 (dd, <semantics>J=12.3<annotation encoding="application / x-tex">J = 12.3< / annotation>< / semantics>, 6.3 Hz, 1H), 3.51 – 3.45 (m, 3H), 3.24 (ddt, <semantics>J=6.7<annotation encoding="application / x-tex">J = 6.7< / annotation>< / semantics>, 4.2, 2.6 Hz, 1H), 2.83 (dd, <semantics>J=5.0<annotation encoding="application / x-tex">J = 5.0< / annotation>< / semantics>, 4.2 Hz, 1H), 2.68 (dd, <semantics>J=5.0<annotation encoding="application / x-tex">J = 5.0< / annotation>< / semantics>) <semantics>=5.0,2.6 Hz,1H),1.68−1.51 (m, 4H).LCMS (ESI) [M+H]+=507.05, Found<annotation encoding="application / x-tex">= 5.0, 2.6 \text{ Hz}, 1\text{H}), 1.68 - 1.51 \text{ (m, 4H).LCMS (ESI) } [\text{M} + \text{H}]^{+} = 507.05, \text{ Found}< / annotation>< / semantics> <semantics>=506.88.<annotation encoding="application / x-tex">=506.88.< / annotation>< / semantics> Example 41: greenhouse experiments A herbicidal activity test method for the compounds of the present invention was as follows: Seed Treatment; pre-emergence: quantitative seeds of gramineous weeds (Echinochloa crusgalli, Eleusine indica, Digitaria sanguinalis, Alopecurus japonicus, Beckmannia syzigachne, Leptochloa chinensis, Polypogon fugax, Alopecurus aequalis, Lolium multiflorum, and Poa annua), broad-leaved weeds (Eclipta prostrata, Amaranthus retroflexus, Brassica juncea, Malachium aquaticum, Conyza canadensis, and Sesbania cannabina), and Cyperus iria were sown in plastic pots having a diameter of 7 cm and holes at the bottom and filled with nutrient soil (sandy soil, pH 6.1, organic matter 1%) respectively, the seeds were covered with an appropriate amount of soil after being sown, then the soil was wetted with water from the bottom, the seeds were cultured in a constant-temperature illuminated culture room for 24 h, and the soil was sprayed by using a 3WP-2000 traveling spray tower produced by the Nanjing Institute of Agricultural Mechanization of the Ministry of Agriculture, where a rotational speed of a main shaft was 96 mm / r, a spray height was 300 mm, an effective spraying range of a nozzle was 350 mm, a spray area was 0.35 m2, and a flow rate at the nozzle was 390 mL / min. Post-emergence: an appropriate quantity of seeds of gramineous weeds (Echinochloa crusgalli, Eleusine indica, Digitaria sanguinalis, Alopecurus japonicus, Beckmannia syzigachne, Leptochloa chinensis, Polypogon fugax, Alopecurus aequalis, Lolium multiflorum, and Poa annua), broad-leaved weeds (Eclipta prostrata, Amaranthus retroflexus, Brassica juncea, Malachium aquaticum, Conyza canadensis, and Sesbania cannabina), and Cyperus iria were sown in plastic pots having a diameter of 7 cm and holes at the bottom and filled with nutrient soil (sandy soil, pH 6.1, organic matter 1%) respectively, the seeds were covered with an appropriate amount of soil after being sown, then the soil was wetted with water from the bottom, the seeds were cultured in a constant-temperature illuminated culture room until a 2-4 leaf stage, and stems and leaves underwent spray treatment. After the treatment, the test materials were placed in a laboratory and cultured in the constant-temperature illuminated culture room after the liquid was naturally dry in the shade, and results were determined 21 days later. Classification standards for prevention and control effects: A indicates that the inhibition rate was greater than or equal to 85% to 100%; B indicates that the inhibition rate was greater than or equal to 70% to less than 85%; C indicates that the inhibition rate was greater than or equal to 55% to less than 70%; D indicates that the inhibition rate was less than 55%. The test results showed that the compounds of the general formula (I) generally had excellent prevention and control effects on various weeds at a dose of 30 g a.i. / hm2, reaching class A. According to the foregoing test method, a parallel experiment was carried out on herbicidal activities of some compounds of the general formula (I), the compound Butafenacil (compound 47 in the patent specification) specifically disclosed in US5183492A, and the compound CK (compound 1 in the patent specification) specifically disclosed in US5183492A, at application doses of 7.5 g a.i. / ha and 15 g a.i. / ha. Results were shown in Table 2: Table 2: Herbicidal activities of some compounds of the general formula (I) and control compounds (post-emergence, fresh weight inhibition rate%) [Image disponible dans le document PDF, Image available in the PDF document] Described above are preferred embodiments of the present invention. It should be noted that, for those of ordinary skill in the art, many variations and improvements may be made without departing from the conception of the present invention, and the variations and improvements fall into the protection scope of the present invention.

Claims

<pat:ClaimStatement>What is claimed is:< / pat:ClaimStatement> <pat:Claims com:id="claims"> <pat:Claim com:id="CLM-00001"> <pat:ClaimNumber>1< / pat:ClaimNumber> <pat:ClaimText>1. A uracil compound containing a carboxylate fragment, a structure of which is shown in the following general formula (I): [Image disponible dans le document PDF, Image available in the PDF document] in the formula: R1 and R2 are each independently hydrogen or methyl; or R1 and R2 together with the carbon atom they are attached form a 3-membered carbocycle; <semantics>R3<annotation encoding="application / x-tex">R_3< / annotation>< / semantics> is <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> haloalkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkenoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> haloalkenoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkynoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> haloalkynoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl <semantics>S(O)n<annotation encoding="application / x-tex">S(O)_n< / annotation>< / semantics> <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C3−6<annotation encoding="application / x-tex">C_{3-6}< / annotation>< / semantics> oxygen-containing cycloalkyl <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, or <semantics>C3−9<annotation encoding="application / x-tex">C_{3-9}< / annotation>< / semantics> oxygen-containing cycloalkyl; n=0, 1, or 2; and when R1 is hydrogen and R2 is methyl, the chiral carbon atom connected thereto may be selected from either an R configuration or an S configuration, or a mixture of the two; and in the mixture, a ratio of R to S is 1:99 to 99:

1. < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00002"> <pat:ClaimNumber>2< / pat:ClaimNumber> <pat:ClaimText>2. The uracil compound containing a carboxylate fragment according to claim 1, wherein R1 and R2 are each independently hydrogen or methyl; or R1 and R2 together with the carbon atom they are attached form a 3-membered carbocycle; <semantics>R3<annotation encoding="application / x-tex">R_3< / annotation>< / semantics> is <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> haloalkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkenoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> haloalkenoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkynoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> haloalkynoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C3−6<annotation encoding="application / x-tex">C_{3-6}< / annotation>< / semantics> oxygen-containing cycloalkyl <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, or <semantics>C3−9<annotation encoding="application / x-tex">C_{3-9}< / annotation>< / semantics> oxygen-containing cycloalkyl; and when R1 is hydrogen and R2 is methyl, the chiral carbon atom connected thereto may be selected from either an R configuration or an S configuration, or a mixture of the two; and in the mixture, a ratio of R to S is 1:99 to 99:

1. < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00003"> <pat:ClaimNumber>3< / pat:ClaimNumber> <pat:ClaimText>3. The uracil compound containing a carboxylate fragment according to claim 1, wherein <semantics>R1<annotation encoding="application / x-tex">R_1< / annotation>< / semantics> and <semantics>R2<annotation encoding="application / x-tex">R_2< / annotation>< / semantics> are each independently hydrogen or methyl; <semantics>R3<annotation encoding="application / x-tex">R_3< / annotation>< / semantics> is <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> haloalkoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkenoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> haloalkenoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> alkynoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C2−6<annotation encoding="application / x-tex">C_{2-6}< / annotation>< / semantics> haloalkynoxy <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, <semantics>C3−6<annotation encoding="application / x-tex">C_{3-6}< / annotation>< / semantics> oxygen-containing cycloalkyl <semantics>C1−3<annotation encoding="application / x-tex">C_{1-3}< / annotation>< / semantics> alkyl, or <semantics>C3−9<annotation encoding="application / x-tex">C_{3-9}< / annotation>< / semantics> oxygen-containing cycloalkyl; and when R1 is hydrogen and R2 is methyl, the chiral carbon atom connected thereto may be selected from either an R configuration or an S configuration, or a mixture of the two; and in the mixture, a ratio of R to S is 1:99 to 99:

1. < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00004"> <pat:ClaimNumber>4< / pat:ClaimNumber> <pat:ClaimText>4. A method for preparing the uracil compound containing a carboxylate fragment according to any one of claims 1-3, wherein the method comprises a contact reaction between the carboxylic acid compound shown in formula (II) and a different substituted alcohol, halogenated, or sulfonate compound in the presence of a solvent, [Image disponible dans le document PDF, Image available in the PDF document] wherein in the general formulas (I) and (II), the definitions of R1, R2, and R3 are the same as those in claim 1. < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00005"> <pat:ClaimNumber>5< / pat:ClaimNumber> <pat:ClaimText>5. The method according to claim 4, wherein the reaction temperature is 0-160°C. < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00006"> <pat:ClaimNumber>6< / pat:ClaimNumber> <pat:ClaimText>6. The method according to claim 4 or 5, wherein the reaction time is 2-15 h. < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00007"> <pat:ClaimNumber>7< / pat:ClaimNumber> <pat:ClaimText>7. The method according to any one of claims 4-6, wherein the reaction solvent comprises dichloromethane, 1,2-dichloroethane, tetrahydrofuran, acetonitrile, 1,4-dioxane, toluene, o-xylene, m-xylene, p-xylene, n-heptane, n-octane, n-nonane, or any combination thereof. < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00008"> <pat:ClaimNumber>8< / pat:ClaimNumber> <pat:ClaimText>8. The method according to any one of claims 4-7, wherein the molar ratio of the carboxylic acid compound shown in formula (II) to the different substituted alcohol, halogenated, or sulfonate compound is 1:(1-4). < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00009"> <pat:ClaimNumber>9< / pat:ClaimNumber> <pat:ClaimText>9. A use of the uracil compound containing a carboxylate fragment according to any one of claims 1-3 in prevention and control of weeds. < / pat:ClaimText> < / pat:Claim> <pat:Claim com:id="CLM-00010"> <pat:ClaimNumber>10< / pat:ClaimNumber> <pat:ClaimText>10. A composition, comprising the uracil compound containing a carboxylate fragment according to any one of claims 1-3 as the active ingredient, wherein the weight percentage content of the active ingredient in the composition is 0.1-99.9%. < / pat:ClaimText> < / pat:Claim> < / pat:Claims>