KR20190056329A - Herbicidal composition - Google Patents

Abstract

The purpose of the present invention is to provide a herbicidal composition which can be stored for a long period of time by having excellent stability while maintaining excellent herbicidal activity as a herbicidal composition comprising a herbicidal active material which belongs to a sulfonylurea-based compound. The present invention relates to a herbicidal composition comprising a pyridine sulfonylurea compound represented by chemical formula 1 as an active ingredient, wherein the pyridine sulfonylurea compound is included as an isomer mixture of erythro-form and threo-form, and the erythro-form is included in an amount of 92 wt% or more of the isomer mixture. In chemical formula 1, n indicates an integer of 1 to 3, R is hydrogen or an alkyl group having 1 to 4 carbon atoms, R′ is hydrogen, an alkyl group having 1 to 4 carbon atoms, a haloalkyl group having 1 to 3 carbon atoms, a halogen group or an alkoxy group having 1 to 2 carbon atoms, and X and Y are each independently an alkyl group having 1 to 2 carbon atoms, an alkoxy group having 1 to 2 carbon atoms, a halogen group having 1 to 2 carbon atoms, or a halogen group.

Description

[0001] HERBICIDAL COMPOSITION [0002]

The present invention relates to a herbicidal composition comprising a herbicidally active ingredient exhibiting excellent herbicidal activity.

In crop cultivation techniques, it is important to protect crops by controlling weeds that inhibit the growth of crops. Herbicidal active substances have been developed for effective control of crops and safe crops in order to reduce damage such as loss of yield or loss of crops caused by weeds caused by weeds in the cultivation area of crops. A large number of herbicidal compounds developed to date have been registered for certain crops and are used for weed control. Herbicidal active substances for use in the control of weeds occurring in the cultivation areas of such specific crops are preferably herbicidal, broadly herbaceous, and safe for the environment and crops.

Meanwhile, the herbicidal composition containing the herbicidal active material as described above may be formulated into a wettable powder, an emulsifiable concentrate, a water-dispersible granule, a granule, or a suspension concentrate. Has been developed and used as a herbicide. However, in the case of a wettable powder, an emulsion, and a granular wettable powder, it is generally diluted with water to a predetermined concentration and is produced as a spray liquid. However, since the spray liquid is large, uniformly spraying the liquid onto the entire surface of the target paddy field or field may cause excessive cost and time have. In the case of granules, the problem of solubilizing agent, emulsion and granular wetting agent could be solved, but the herbicidal active ingredient content is relatively low on the basis of total herbicide and auxiliary agent for forming herbicide must be included There is a problem that the manufacturing process such as pulverization, mixing, aging, assembling, drying and classifying is complicated, and scattering unevenness occurs. In order to overcome the problems of the formulations, a suspension concentrate formulation has been developed which is relatively simple to manufacture, environmentally friendly, and simple and efficient at the time of spraying. On the other hand, securing the stability of the herbicidal composition even when stored for a long period of time is an important problem when utilized as herbicides of various formulations.

The compound of formula (a) [ISO proposal name: flucetosulfuron] is a herbicidally active substance belonging to the sulfonylurea system, and Korean Patent No. 10-0399366 (Application No. 10-2000-0059990) It has already been described as a substance.

(A)

The flutosulfuron is safe for these crops in soil or foliar treatment for rice, wheat, barley (suitable dose: 10 to 40 g ai / ha) and grass (suitable dosage: 50-200 g ai / It is known to have excellent herbicidal effect on broad-leaved weeds such as broad-leaved weeds, herbaceous weeds, weed seeds, weeds, annuals and perennial weeds.

However, securing the stability of a herbicidal composition containing a herbicidally active substance belonging to the sulfonylurea group as described above still remains a problem. In particular, in the case of a suspension concentrate (SC) formulation, stability is further reduced by hydrolysis under high-temperature storage conditions, which makes it difficult to store for a long period of time.

Korean Patent Registration No. 10-0399366

The present invention provides a herbicidal composition comprising a herbicidally active substance belonging to the sulfonylurea class, which has excellent herbicidal activity and is excellent in stability and can be stored for a long period of time.

The present invention relates to a pyridine sulfonylurea compound represented by the following formula (1) as an active ingredient, wherein the pyridine sulfonylurea compound is an isomer mixture of an erythro-form and a threo-form, Wherein the erythro-form comprises at least 92% by weight of the isomer mixture.

[Chemical Formula 1]

n represents an integer of 1 to 3,

R is hydrogen or an alkyl group having 1 to 4 carbon atoms,

R 'is hydrogen, an alkyl group having 1 to 4 carbon atoms, a haloalkyl group having 1 to 3 carbon atoms, a halogen group or an alkoxy group having 1 to 2 carbon atoms,

X and Y each independently represent an alkyl group having 1 to 2 carbon atoms, an alkoxy group having 1 to 2 carbon atoms, a haloalkoxy group having 1 to 2 carbon atoms, or a halogen group.

According to the present invention, it is possible to provide a herbicidal composition which has excellent herbicidal activity, has a low decomposition rate even when stored at a high temperature for a long period of time, and can secure excellent stability even in formulation of a suspension concentrate (SC).

Hereinafter, the present invention will be described in detail in order to facilitate understanding of the present invention. Herein, terms and words used in the present specification and claims should not be construed to be limited to ordinary or dictionary meanings, and the inventor may appropriately define the concept of the term to describe its own invention in the best way. It should be construed as meaning and concept consistent with the technical idea of the present invention.

The herbicidal composition of the present invention comprises a pyridine sulfonylurea compound represented by the following formula (1) as an active ingredient, and the pyridine sulfonylurea compound is an isomer mixture of an erythro-form and a threo-form , And the Erythro-form comprises at least 92% by weight of the isomer mixture.

[Chemical Formula 1]

R is hydrogen, an alkyl group having 1 to 4 carbon atoms, a haloalkyl group having 1 to 3 carbon atoms, a halogen group, or a halogenated alkyl group having 1 to 3 carbon atoms. In the formula, n is an integer of 1 to 3, R is hydrogen or an alkyl group having 1 to 4 carbon atoms, And X and Y each independently represent an alkyl group having 1 to 2 carbon atoms, an alkoxy group having 1 to 2 carbon atoms, a haloalkoxy group having 1 to 2 carbon atoms, or a halogen group.

More preferably, the pyridine sulfonylurea compound represented by Formula 1 is represented by Formula 1, wherein n is an integer of 1 or 2, R is hydrogen or a methyl group, R 'is hydrogen, a halogen group or a methyl group, X And Y may each be a methoxy group.

More preferably, the pyridine sulfonylurea compound represented by Formula 1 is represented by Formula 1, wherein n is an integer of 1 or 2, R is methyl, R 'is hydrogen, Cl, Br or a methyl group, X and Y may each be methoxy.

The pyridine sulfonylurea compound represented by the above formula (1) can be produced, for example, by reacting N - [(4,6-dimethoxypyrimidin-2- yl) aminocarbonyl] -2- (2-fluoro- (2-fluoro-1-hydroxy-n-propyl) pyridine-3-sulfonamide, N - [(4,6- dimethoxypyrimidin- 2- (2-fluoro-1- (3-methoxyphenyl) pyridine-3-sulfonamide and N- (4,6- dimethoxypyrimidin- 2- (2-fluoro-1- (4-fluorophenyl) propyl) oxy] -pyridine- (3-methoxypropion) oxy-n-propyl) pyridine-3-sulfonamide and N - [(4,6- dimethoxypyrimidin- Methoxyacetoxy-n-propyl) pyridine-3-sulfonamide, N - [(4,6- dimethoxypyrimidin-2- yl) aminocarbonyl] 2- (2-fluoro-1-methoxyacetoxy-n-propyl) pyridine- (2-fluoro-1-methoxyacetoxy-n-propyl) amide, and N - [(4,6- dimethoxypyrimidin- ) Pyridine-3-sulfonamide.

More preferably, the pyridine sulfonylurea compound represented by the formula (1) may be a compound represented by the following formula (2) [ISO proposal name: flucetosulfuron].

(2)

Since the compound of Formula 1 contains two asymmetric carbons, it may exist as an isomer of erythro-form or threo-form.

The herbicidal composition of the present invention is characterized in that the compound represented by Formula 1 is contained in an isomer mixture of an Erythro-form and a threo-form, wherein the Erythro- Of the total weight of the composition. More preferably, the Erythro-form may comprise at least 95% by weight of the isomeric mixture, more preferably the Erythro-form comprises from 95% to 99% by weight of the isomeric mixture, ≪ / RTI >

As described above, the Erythro-form and the threo-form isomer mixture containing the erythro-form in an amount of not less than 92% by weight not only has excellent herbicidal activity, The degradation rate can be reduced and the stability can be ensured.

In the case where the compound represented by Formula 1 is contained in the form of an erythro-form alone rather than in the form of an isomer mixture of an erythro-form and a threo-form, the production efficiency is very low. , And when they are contained in the form of a threo-form alone, the herbicidal activity is lowered and the decomposition rate is greatly increased, resulting in a problem of low stability. In addition, although it exists as an isomer mixture of Erythro-form and threo-form, when the isomer mixture contains less than 92% by weight of erythro-form, the herbicidal activity is lowered, In particular, in the case of liquid formulations, the stability is further lowered by hydrolysis, and storage of high temperature for a long time is difficult.

In the present invention, the herbicidal composition comprising the isomeric mixture of the compound represented by Formula 1 may be used as a conventional herbicidal composition. The herbicidal composition comprising the isomer mixture may further be used as a herbicide of various formulations, if necessary, further comprising additives, which are commonly used in the field of carriers, surfactants or formulation techniques. The carrier and additive may be solid or liquid and may be an ingredient useful in the field of formulation technology, such as natural or synthetic inorganic substances, solvents, dispersants, wetting agents, adhesives, thickeners, binders and the like.

For example, the herbicide composition can be applied to a variety of herbicidal compositions such as suspension concentrate, spreading oil, wettable powder, water-dispersible granule, dispersible powder, spraying agent, granule, a granule, and a tablet. More preferably, it may be a suspension concentrate, and in the case of the suspension concentrate, it may further comprise a buffer solution, a surfactant, and a cryoprotectant. Suspension concentrate generally has a relatively simple manufacturing process, is environmentally friendly, has advantages of being simple and efficient at the time of spraying, but has a problem of poor stability due to decomposition due to hydrolysis. However, the herbicidal composition of the present invention contains an Erythro-form in an Erythro-form and a threo-form isomer mixture in an amount of 92 wt% or more, In the case of the suspension concentrate formulation, the degradation rate due to hydrolysis is lowered and the stability is greatly improved, so that it can be stored at a high temperature for a long time.

The various formulations of the herbicidal compositions may be prepared according to known methods, for example by intimately mixing and / or grinding the active ingredient with a solvent, solid carrier, surfactant or other additive.

Usable as the solvent are aromatic hydrocarbons such as xylene mixture or substituted naphthalene; Alcohols such as ethanol, ethylene glycol, ethylene glycol monomethyl ether or ethylene glycol monoethyl ether and glycols and their ethers and esters; Ketones such as cyclohexanone, strong polar solvents such as N-methyl-2-pyrrolidone, dimethylsulfoxide or dimethylformamide, and epoxidized or non-epoxidized vegetable oils such as epoxidized coconut oil or soybean oil; Or water. Such a solvent can be used as a solvent for a liquid form or as a co-solvent for a granular formulation.

The solid carriers commonly used in such spraying and granulating formulations are typically ground natural minerals such as talc, kaolin, montmorillonite, pyrophyllite, bentonite, or calcium carbonate, adsorbent carriers such as zeolites, or sand. In addition, a number of pre-milled inorganic or organic materials may be used.

The surfactant may be selected from nonionic, cationic and / or anionic surfactants which exhibit good dispersing, wetting and lubricating properties depending on the nature of the compound of formula (1) to be formulated.

A more preferred method of administering the herbicidal composition comprising the isomeric mixture of compounds of Formula 1 is to use the liquid formulation to wet the habitat of the plant or to incorporate the active ingredient into the soil in the form of a solid, And through the stem to soil or water to reach the plant. Alternatively, the herbicidal activity can be shown by direct administration to the leaves of plants (foliar application). The frequency and rate of administration may vary depending on the biological characteristics of the plant, the climate, and the soil environment.

The present application will now be described with reference to specific embodiments, which are not intended to limit the scope of the invention. On the contrary, the invention is intended to cover all alternatives and modifications that fall within the scope of the claims. Accordingly, the following is presented to illustrate the practice of the present application for purposes of illustration of the specific embodiments, and to provide those which are believed to be useful and readily understood descriptions of the process and conceptual aspects thereof.

The following examples are presented to provide those of ordinary skill in the art with a complete disclosure and description of how the compounds, compositions, and methods provided herein are made and evaluated, and are intended to be exemplary only. Accordingly, the embodiments are by no means intended to limit the scope of what the inventors regard as their invention. There are many variations and combinations of conditions that may be utilized to optimize reaction conditions such as, for example, component concentrations, desired solvents, solvent mixtures, temperatures, pressures, and other reaction parameters and product properties such as purity, yield, . These are also considered to be within the scope of this disclosure. Any combination of the above-described elements in all possible variations is encompassed by the present invention unless otherwise indicated herein or otherwise clearly contradicted by context.

Example  One

K ₂ HPO ₄ and KH ₂ PO ₄ were added to make a total of 1 L solution to prepare a 0.1 M phosphate buffer solution. To 65.8 parts by weight of the buffer solution, 3.0 parts by weight of CR-DOS70P (Di (2-ethylhexyl) sulfosuccinate, sodium salt, Cas No. 577-11-7), NK-SU500 (sucrose laurate, cas No. 25339-99-5 ) And 0.2 part by weight of a defoaming agent SAG-622 (Momentiv) were added and thoroughly mixed to obtain 1- (3 - {[(4,6-dimethoxy-pyrimidin-2- yl) carbamoyl ] Sulfamoyl} -2-pyridinyl) -2-fluoropropylmethoxyacetate (Flutosulfuron, FTS) in an amount of 96% by weight and a threo-form in an amount of 4% by weight 10.0 parts by weight of an isomer mixture was added thereto and sufficiently mixed using a stirrer. A glass bead was placed in the mill and grinding was carried out until the average particle size was 1 to 2 탆 to prepare a wet part.

Next, to 3.0 parts by weight of PG (propylene glycol, cas no. 57-55-6), 0.1 part by weight of XG (Xanthan Gum, cas no.11138-66-2), 0.1 part by weight of MV [ (Cas no.26172-55-4) and 2-methyl-4-isothiazolin-3-one (cas no.2682-20-4)] were added and sufficiently stirred . Then, 16.7 parts by weight of 0.1 M phosphate buffer was added and sufficiently stirred to prepare a thickened portion.

Next, 30 parts by weight of the boiling point portion was added to 70 parts by weight of the wet part and sufficiently stirred to prepare a herbicidal composition of the liquid wettable powder.

Example  2

The procedure of Example 1 was repeated except that an isomer mixture containing 92 wt% of Erythro-form and 8 wt% of threo-form as FTS was mixed to obtain a liquid herbicide-formulated herbicide A composition was prepared.

Example  3

15 parts by weight of CR-PE62 (Polyethylene-Polypropylene glycol, Cas no. 9003-11-6) was adsorbed in 20 parts by weight of celite 281 (Calcined Diatomite, Cas no. 91053-39-3) (Erythro-form) of Flucetosulfuron (FTS), which is a mixture of [(4,6-dimethoxy-pyrimidin-2-yl) carbamoyl] sulfamoyl} -2-pyridinyl) -2-fluoropropylmethoxyacetate ), 10 parts by weight of an isomer mixture containing 96% by weight of an isomer and 3% by weight of a threo-form, NK-EFW (2-Naphthalenesulfonic acid, polymer with formaldehyde, sodium salt, ), 3 parts by weight of NK-D425 (2-Naphthalenesulfonic acid, polymer with formaldehyde, sodium salt, Cas no.36290-04-7), sodium dodecyl sulfate (CR-SDS) ) And 10 parts by weight of CR-UF100F (Urea-formaldehyde resin (CAS no. 9011-05-6)) were mixed, and the remaining Talc was mixed so that the total amount of the composition was 100 parts by weight. . 10 to 12 parts by weight of water was added to the pulverized mixture, kneaded and granulated using a granulator, followed by hot air drying at a temperature of about 80 캜 to prepare a granular herbicidal composition.

Comparative Example  One

The procedure of Example 1 was repeated except that an isomer mixture containing 88% by weight of Erythro-form and 12% by weight of threo-form as FTS was mixed to prepare a liquid herbicide-formulated herbicide A composition was prepared.

Comparative Example  2

The procedure of Example 1 was repeated, except that an isomer mixture containing 85 wt% Erythro-form and 15 wt% threo-form as FTS was mixed to obtain a liquid herbicide-formulated herbicide A composition was prepared.

Comparative Example  3

The procedure of Example 3 was repeated except that an isomer mixture containing 88 wt% Erythro-form and 12 wt% threo-form was mixed as the FTS, and the herbicide A composition was prepared.

[ Experimental Example : Evaluation of storage stability of herbicidal composition]

In order to evaluate the storage stability of the herbicidal compositions of Examples 1 to 3 and Comparative Examples 1 to 3, the liquid sample was filled in a plastic bottle made of polyethylene (PE), and the granular sample was filled in about 100 g each in a silver foil bag. (± 2) ° C for 4 weeks, respectively, and the area of active ingredient was measured by HPLC (manufacturer: Waters) to evaluate the decomposition rate. The results are shown in Table 1 below.

The HPLC analysis conditions are as follows.

Column: 100 mm x 4.6 mm i.d. &Quot; Capcell Pak " C18 column, 3 mu m particles

Mobile Phase: acetonitrile / water (0.02M ammonium acetate + 0.1M acetic acid) = 32/68

Flow: 1.0 mL / min.

Column Temperature: 30 ℃

Injection Volume: 10 μl

Detector Wavelength: 254 nm

Run time: 20 min.

Decomposition rate after storage at 54 ℃ for 4 weeks (%) Example 1 6.89 Example 2 9.82 Example 3 13.63 Comparative Example 1 9.94 Comparative Example 2 12.24 Comparative Example 3 17.85

Claims (8)

A pyridine sulfonylurea compound represented by the following formula (1) as an active ingredient,
The pyridine sulfonylurea compound is contained in an isomer mixture of Erythro-form and threo-form,
Wherein the erythro-form comprises at least 92% by weight of the isomer mixture.
[Chemical Formula 1]

In the above formula (1), n represents an integer of 1 to 3,
R is hydrogen or an alkyl group having 1 to 4 carbon atoms,
R 'is hydrogen, an alkyl group having 1 to 4 carbon atoms, a haloalkyl group having 1 to 3 carbon atoms, a halogen group or an alkoxy group having 1 to 2 carbon atoms,
X and Y each independently represent an alkyl group having 1 to 2 carbon atoms, an alkoxy group having 1 to 2 carbon atoms, a haloalkoxy group having 1 to 2 carbon atoms, or a halogen group.
The method according to claim 1,
Wherein the erythro-form comprises at least 95% by weight of the isomeric mixture.
The method according to claim 1,
Wherein the erythro-form comprises from 95% to 99% by weight of the isomeric mixture.
The method according to claim 1,
In Formula 1, n is an integer of 1 or 2,
R is hydrogen or a methyl group,
R 'is hydrogen, a halogen group or a methyl group,
X and Y are each methoxy group.
The method according to claim 1,
In Formula 1, n is an integer of 1 or 2,
R is methyl,
R 'is hydrogen, Cl, Br or a methyl group,
X and Y are each methoxy.
The method according to claim 1,
The pyridine sulfonylurea compound represented by the above formula (1)
(2-fluoro-1-methoxyacetoxy-n-propyl) pyridine-3-sulphonamide, N - [(4,6- dimethoxypyrimidin- N- (2-fluoro-1-hydroxyacetoxy-n-propyl) pyridine-3-sulfonamide, N- (2-fluoro-1- (3-hydroxypropion) oxy-n-propyl) pyridine-3-sulfonamide (2-fluoro-1- (3-methoxypropion) oxy-n-propyl) pyridin-3 4-methyl-2- (2-fluoro-1-methoxyacetoxy-n-propyl) Pyridin-3-sulfonamide, N - [(4,6-dimethoxypyrimidin-2-yl) aminocarbonyl] -4-chloro-2- (2-fluoro-1-methoxyacetoxy- -Propyl) pyridine-3-sulfonamide and N - [(4,6-dimethoxypyrimidin-2-yl) aminocarbonyl] 2- (2-fluoro-1-methoxyacetoxy-n-propyl) pyridine-3-sulfonamide.
The method according to claim 1,
The herbicidal composition is formed of at least one herbicidal composition selected from the group consisting of a liquid wettable powder, a water spreading agent, a wetting agent, a granular wettable powder, a powder, a spraying agent, a granule, a granule and a tablet.
The method according to claim 1,
The herbicidal composition is formed into a formulation of a liquid suspension agent (SC) further comprising a buffer, a surfactant and an anti-freezing agent.