JP2021095364A - Azinyl azole compound and pest control agent - Google Patents

Abstract

To provide an azinyl azole compound that has excellent insecticidal activity and/or acaricidal activity, and excellent safety, and can be synthesized in an industrially advantageous manner.SOLUTION: The present disclosure provides a compound represented by the formula (I) or a salt thereof (where X is a halogeno group, a substituted or unsubstituted C1-6 alkyl group or the like, n is an integer of 1-5, Q1 is a substituted or unsubstituted 5-membered heterocyclylene group, A is a substituted or unsubstituted C1-2 alkylene group, Y1 is a nitrogen atom or a group represented by CRa, Y2 is a nitrogen atom or a group represented by CRa, Ra independently represents a hydrogen atom, a halogeno group, or a substituted or unsubstituted C1-6 alkyl group, Q2 is a substituted or unsubstituted 6-membered heteroaryl group).SELECTED DRAWING: None

Description

The present invention relates to azinylazole compounds and pest control agents. More specifically, the present invention has excellent insecticidal activity and / or acaricidal activity, is excellent in safety, and can be synthesized industrially advantageously. Azinylazole compound and pest control containing the same as an active ingredient. Regarding agents.

Various compounds having insecticidal and acaricidal activity have been proposed. In order to put such a compound into practical use as a pesticide, not only is it sufficiently effective, it is unlikely to cause drug resistance, it does not cause phytotoxicity or soil contamination to plants, and it has low toxicity to livestock and fish. Etc. are required.

By the way, a compound having a CAS Registry Number of 1269149-23-6 represented by the following formula (A) is commercially available, but its use is unknown.

Further, Patent Document 1 states that the compound represented by the formula (B) or the like can be used for suppressing ectoparasites in animals.

WO 2017/192385 A1

STEFANI Helio A. et al. "Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition" Tetrahedron Letters, Volume 52, Issue 46, 16 November 2011, Pages 6086-6090

An object of the present invention is to provide an azinylazole compound which is excellent in pest control activity, particularly insecticidal activity and / or acaricidal activity, is excellent in safety, and can be synthesized industrially advantageously. Another object of the present invention is to provide a pest control agent, an insecticide or acaricide, an ectoparasite control agent, or an endoparasite control or control agent containing an azinylazole compound as an active ingredient.

As a result of studies for solving the above problems, the present invention including the following forms has been completed.

（式（I）中、
Ｘは、ハロゲノ基、置換若しくは無置換のＣ１〜６アルキル基、水酸基、置換若しくは無置換のＣ１〜６アルコキシ基、置換若しくは無置換のＣ１〜６アルキルチオ基、置換若しくは無置換のＣ１〜６アルキルスルフィニル基、置換若しくは無置換のＣ１〜６アルキルスルホニル基、置換若しくは無置換のＣ３〜６シクロアルキル基、置換若しくは無置換のＣ３〜６シクロアルキルオキシ基、置換若しくは無置換のＣ３〜６シクロアルキルチオ基、置換若しくは無置換のＣ３〜６シクロアルキルスルフィニル基、置換若しくは無置換のＣ３〜６シクロアルキルスルホニル基、ニトロ基、またはシアノ基を示し、
ｎは、Ｘの数を示し且つ１〜５のいずれかの整数であり、
Ｑ¹は、置換若しくは無置換の５員ヘテロシクリレン基を示し、
Ａは、置換若しくは無置換のＣ１〜２アルキレン基を示し、
Ｙ¹は、窒素原子またはＣＲ^aで表される基を示し、
Ｙ²は、窒素原子またはＣＲ^aで表される基を示し、
Ｒ^aは、それぞれ独立に、水素原子、ハロゲノ基、または置換若しくは無置換のＣ１〜６アルキル基を示し、
Ｑ²は、置換若しくは無置換の６員ヘテロアリール基を示す。） [1] A compound represented by the formula (I) or a salt thereof.

(In formula (I),
X is a halogeno group, a substituted or unsubstituted C1-6 alkyl group, a hydroxyl group, a substituted or unsubstituted C1-6 alkoxy group, a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkyl. Sulfinyl group, substituted or unsubstituted C1-6 alkylsulfonyl group, substituted or unsubstituted C3-6 cycloalkyl group, substituted or unsubstituted C3-6 cycloalkyloxy group, substituted or unsubstituted C3-6 cycloalkylthio Group, substituted or unsubstituted C3-6 cycloalkylsulfinyl group, substituted or unsubstituted C3-6 cycloalkylsulfonyl group, nitro group, or cyano group.
n indicates the number of X and is an integer of 1 to 5.
Q ¹ represents a substituted or unsubstituted 5-membered heterocyclylene group.
A represents a substituted or unsubstituted C1-2 alkylene group.
Y ¹ represents a nitrogen atom or ^a group represented by CR a,
Y ² represents a group represented by ^a nitrogen atom or CR a,
R ^a each independently represent a hydrogen atom, a halogeno group or a substituted or unsubstituted C1~6 alkyl,
Q ² represents a substituted or unsubstituted 6-membered heteroaryl group. )

[2] The compound according to [1] or a salt thereof, wherein ^{Q 1 is a substituted or unsubstituted triazolylen group.}
[3] The compound according to [1] or [2] or a salt thereof, wherein ^{Q 2 is a substituted or unsubstituted pyridyl group or a substituted or unsubstituted pyrimidinyl group.}

[4] A pest control agent containing at least one selected from the compounds according to any one of [1] to [3] as an active ingredient.
[5] An insecticide or acaricide containing at least one selected from the compounds according to any one of [1] to [3] as an active ingredient.
[6] An ectoparasite control agent containing at least one selected from the compounds according to any one of [1] to [3] as an active ingredient.
[7] An endoparasite control or extermination agent containing at least one selected from the compounds according to any one of [1] to [3] as an active ingredient.

The azinylazole compound of the present invention has a function of controlling pests that pose a problem in terms of crops and hygiene. The control agent containing the azinylazole compound of the present invention can effectively control pests, especially agricultural pests and mites, at a lower concentration, and further ectoparasites and endoparasites that may harm humans and animals. Insects can be effectively controlled.

The azinylazole compound of the present invention is a compound represented by the formula (I) or a salt thereof.

Here, the term "unsubstituted" means that it is only a parent group. When there is no description of "substitution" and only the name of the parent group is described, it means "unsubstituted" unless otherwise specified.
On the other hand, the term "substituent" means that any hydrogen atom of the parent group is substituted with a group (substituent) having the same or different structure as the mother nucleus. Therefore, a "substituent" is another group attached to the parent group. The substituent may be one or two or more. The two or more substituents may be the same or different.
Terms such as "C1 to 6" indicate that the number of carbon atoms of the parent group is 1 to 6 or the like. This number of carbon atoms does not include the number of carbon atoms present in the substituent. For example, a butyl group having an ethoxy group as a substituent is classified as a C2 alkoxy C4 alkyl group.

The "substituent" is chemically acceptable and is not particularly limited as long as it has the effect of the present invention. The groups that can be "substituents" are illustrated below.
C1-6 such as methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, s-butyl group, i-butyl group, t-butyl group, n-pentyl group, n-hexyl group, etc. Alkyl group;
Vinyl group, 1-propenyl group, 2-propenyl group (allyl group), 1-butenyl group, 2-butenyl group, 3-butenyl group, 1-methyl-2-propenyl group, 2-methyl-2-propenyl group, etc. C2-6 alkenyl groups;
C2-6 alkynyl groups such as ethynyl group, 1-propynyl group, 2-propynyl group, 1-butynyl group, 2-butynyl group, 3-butynyl group, 1-methyl-2-propynyl group;

C3-8 cycloalkyl groups such as cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cubicyl group;
Phenyl group, naphthyl group;
Benzyl group, phenethyl group;
3-6 member heterocyclyl group;
3 to 6 member heterocyclyl C1 to 6 alkyl groups;

Hydroxy group;
C1-6 alkoxy groups such as methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, s-butoxy group, i-butoxy group, t-butoxy group;
C2-6 alkenyloxy groups such as vinyloxy group, allyloxy group, propenyloxy group, butenyloxy group;
C2-6 alkynyloxy groups such as ethynyloxy group and propargyloxy group;
Phenoxy group, naphthoxy group;
Phenyl C1-6 alkoxy groups such as benzyloxy group and phenethyloxy group;
5- to 6-membered heteroaryloxy groups such as thiazolyloxy groups and pyridyloxy groups;
5-6 membered heteroaryl C1-6 alkyloxy groups such as thiazolylmethyloxy group, pyridylmethyloxy group;

Holmil group;
C1-6 alkylcarbonyl groups such as acetyl group, propionyl group;
Formyloxy group;
C1-6 alkylcarbonyloxy groups such as acetyloxy group, propionyloxy group;
Benzoyl group;
C1-6 alkoxycarbonyl groups such as methoxycarbonyl group, ethoxycarbonyl group, n-propoxycarbonyl group, i-propoxycarbonyl group, n-butoxycarbonyl group, t-butoxycarbonyl group;
C1-6 alkoxycarbonyloxy groups such as methoxycarbonyloxy group, ethoxycarbonyloxy group, n-propoxycarbonyloxy group, i-propoxycarbonyloxy group, n-butoxycarbonyloxy group, t-butoxycarbonyloxy group;
Carboxyl group;

Halogeno groups such as fluoro group, chloro group, bromo group, iod group;
C1-6 haloalkyl groups such as chloromethyl group, chloroethyl group, trifluoromethyl group, 1,2-dichloro-n-propyl group, 1-fluoro-n-butyl group;
C2-6 haloalkenyl groups such as 2-chloro-1-propenyl group, 2-fluoro-1-butenyl group;
C2-6 haloalkynyl groups such as 4,4-dichloro-1-butynyl group, 4-fluoro-1-pentynyl group, 5-bromo-2-pentynyl group;
C1-6 haloalkoxy groups such as trifluoromethoxy group, 2-chloro-n-propoxy group, 2,3-dichlorobutoxy group;
C2-6 haloalkenyloxy groups such as 2-chloropropenyloxy group, 3-bromobutenyloxy group;
C1-6 haloalkylcarbonyl groups such as chloroacetyl groups, trifluoroacetyl groups, trichloroacetyl groups;

Amino group;
C1-6 alkyl-substituted amino groups such as methylamino group, dimethylamino group, diethylamino group;
Phenylamino groups such as anilino groups;
Phenyl C1-6 alkylamino groups such as benzylamino group, phenethylamino group;
Formylamino group;
C1-6 alkylcarbonylamino groups such as acetylamino group, propanoylamino group, butyrylamino group, i-propylcarbonylamino group;
C1-6 alkoxycarbonylamino groups such as methoxycarbonylamino groups, ethoxycarbonylamino groups, n-propoxycarbonylamino groups, i-propoxycarbonylamino groups;
Aminocarbonyl group having an unsubstituted or substituent such as a carbamoyl group, a dimethylaminocarbonyl group, a phenylaminocarbonyl group, an N-phenyl-N-methylaminocarbonyl group;
Imino C1-6 alkyl groups such as iminomethyl group, (1-imino) ethyl group, (1-imino) -n-propyl group;
N-hydroxy-iminomethyl group, (1- (N-hydroxy) -imino) ethyl group, (1- (N-hydroxy) -imino) propyl group, N-methoxy-iminomethyl group, (1- (N-methoxy) -Imino) N-hydroxyimino C1-6 alkyl group substituted or unsubstituted such as ethyl group;
Amino carbonyloxy group;
C1-6 alkyl-substituted aminocarbonyloxy groups such as ethylaminocarbonyloxy group, dimethylaminocarbonyloxy group;

Mercapto group;
C1-6 alkylthio groups such as methylthio group, ethylthio group, n-propylthio group, i-propylthio group, n-butylthio group, i-butylthio group, s-butylthio group, t-butylthio group;
C1-6 haloalkylthio groups such as trifluoromethylthio group, 2,2,2-trifluoroethylthio group;
Phylphenylthio group, naphthylthio group;
5- to 6-membered heteroarylthio groups such as thiazolylthio groups and pyridylthio groups;

C1-6 alkylsulfinyl groups such as methylsulfinyl group, ethylsulfinyl group, t-butylsulfinyl group;
C1-6 haloalkylsulfinyl groups such as trifluoromethylsulfinyl groups, 2,2,2-trifluoroethylsulfinyl groups;
Phenylsulfinyl group;
5- to 6-membered heteroarylsulfinyl groups such as thiazolylsulfinyl groups, pyridylsulfinyl groups;

C1-6 alkylsulfonyl groups such as methylsulfonyl groups, ethylsulfonyl groups, t-butylsulfonyl groups;
C1-6 haloalkylsulfonyl groups such as trifluoromethylsulfonyl groups, 2,2,2-trifluoroethylsulfonyl groups;
Phenylsulfonyl group;
5- to 6-membered heteroarylsulfonyl groups such as thiazolylsulfonyl groups and pyridylsulfonyl groups;
C1-6 alkylsulfonyloxy groups such as methylsulfonyloxy groups, ethylsulfonyloxy groups, t-butylsulfonyloxy groups;
C1-6 haloalkylsulfonyloxy groups such as trifluoromethylsulfonyloxy groups, 2,2,2-trifluoroethylsulfonyloxy groups;

Tri-C1-6 alkyl-substituted silyl groups such as trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group;
Triphenylsilyl group;
Pentafluorosulfanil group;
Cyano group; Nitro group;

Further, in these "substituents", any hydrogen atom in the substituent may be substituted with a group having a different structure. Examples of the "substituent" in this case include a C1-6 alkyl group, a C1-6 haloalkyl group, a C1-6 alkoxy group, a C1-6 haloalkoxy group, a halogeno group, a cyano group, a nitro group and the like.

Further, the above-mentioned "3 to 6-membered heterocyclyl group" is a 3-membered ring, a 4-membered ring, 5 containing 1 to 4 heteroatoms selected from the group consisting of nitrogen atom, oxygen atom and sulfur atom as ring constituent atoms. It is a member ring or a 6-member ring. The heterocyclyl group may be monocyclic or polycyclic. The polycyclic heterocyclyl group may have any of a saturated alicyclic ring, an unsaturated alicyclic ring, or an aromatic ring as long as at least one ring is a heterocyclic ring. Examples of the "3- to 6-membered heterocyclyl group" include a 3- to 6-membered saturated heterocyclyl group, a 5- to 6-membered heteroaryl group, and a 5- to 6-membered partially unsaturated heterocyclyl group.

Examples of the 3- to 6-membered saturated heterocyclyl group include an aziridinyl group, an epoxy group, a pyrrolidinyl group, a tetrahydrofuranyl group, a thiazolidinyl group, a piperidyl group, a piperazinyl group, a morpholinyl group, a dioxolanyl group and a dioxanyl group.

Examples of the 5-membered heteroaryl group include a pyrrolyl group, a furyl group, a thienyl group, an imidazolyl group, a pyrazolyl group, an oxazolyl group, an isooxazolyl group, a thiazolyl group, an isothiazolyl group, a triazolyl group, an oxadiazolyl group, a thiadiazolyl group and a tetrazolyl group. Can be done.
Examples of the 6-membered heteroaryl group include a pyridyl group, a pyrazinyl group, a pyrimidinyl group, a pyridadinyl group, a triazinyl group and the like.

[X, n]
X is a halogeno group, a substituted or unsubstituted C1-6 alkyl group, a hydroxyl group, a substituted or unsubstituted C1-6 alkoxy group, a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkyl. Sulfinyl group, substituted or unsubstituted C1-6 alkylsulfonyl group, substituted or unsubstituted C3-6 cycloalkyl group, substituted or unsubstituted C3-6 cycloalkyloxy group, substituted or unsubstituted C3-6 cycloalkylthio It represents a group, a substituted or unsubstituted C3-6 cycloalkylsulfinyl group, a substituted or unsubstituted C3-6 cycloalkylsulfonyl group, a nitro group, or a cyano group.
n indicates the number of X and is an integer of 1 to 5. When n is 2 or more, X may be the same or different from each other.

Examples of the "halogeno group" in X include a fluoro group, a chloro group, a bromo group, an iod group and the like.

The "C1-6 alkyl group" in X may be a straight chain or a branched chain. The "C1-6 alkyl group" in X includes a methyl group, an ethyl group, an n-propyl group, an n-butyl group, an n-pentyl group, an n-hexyl group, an i-propyl group, an i-butyl group, and s-. Butyl group, t-butyl group, i-pentyl group, neopentyl group, 2-methylbutyl group, i-hexyl group and the like can be mentioned.

Examples of the "C1-6 alkoxy group" in X include a methoxy group, an ethoxy group, an n-propoxy group, an n-butoxy group, an n-pentyloxy group, an n-hexyloxy group, an i-propoxy group, and an i-butoxy group. Examples thereof include an s-butoxy group, a t-butoxy group, and an i-hexyloxy group.

Examples of the "C1-6 alkylthio group" in X include a methylthio group, an ethylthio group, an n-propylthio group, an n-butylthio group, an n-pentylthio group, an n-hexylthio group and an i-propylthio group.

Examples of the "C1 to 6 alkylsulfinyl group" in X include a methylsulfinyl group, an ethylsulfinyl group, and a t-butylsulfinyl group.

Examples of the "C1 to 6 alkylsulfonyl group" in X include a methylsulfonyl group, an ethylsulfonyl group, and a t-butylsulfonyl group.

As a substituent on "C1-6 alkyl group", "C1-6 alkoxy group", "C1-6 alkylthio group", "C1-6 alkylsulfinyl group", or "C1-6 alkylsulfonyl group" in X , Fluorogen groups such as fluoro group, chloro group, bromo group, iodo group; hydroxyl group; methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, s-butoxy group, i-butoxy group, C1-6 alkoxy groups such as t-butoxy group; C1-6 haloalkoxy groups such as 2-chloro-n-propoxy group, 2,3-dichlorobutoxy group, trifluoromethoxy group; phenyl group; 4-chlorophenyl group, A "phenyl group substituted with a halogeno group, a C1-6 haloalkyl group, or a C1-6 haloalkoxy group" such as a 4-trifluoromethylphenyl group, a 4-trifluoromethoxyphenyl group; or a cyano group; is preferable.

Examples of the "C3-8 cycloalkyl group" in X include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group and the like.
Examples of the "C3 to 8 cycloalkyloxy group" in X include a cyclopropyloxy group, a cyclobutyloxy group, a cyclopentyloxy group, a cyclohexyloxy group and the like.

Examples of the "C3-8 cycloalkylthio group" in X include a cyclopropylthio group, a cyclobutylthio group, a cyclopentylthio group, a cyclohexylthio group and the like.
Examples of the "C3-8 cycloalkylsulfinyl group" in X include a cyclopropylsulfinyl group, a cyclobutylsulfinyl group, a cyclopentylsulfinyl group, a cyclohexylsulfinyl group and the like.
Examples of the "C3-8 cycloalkylsulfonyl group" in X include a cyclopropylsulfonyl group, a cyclobutylsulfonyl group, a cyclopentylsulfonyl group, a cyclohexylsulfonyl group and the like.

"C3-8 cycloalkyloxy group", "C3-8 cycloalkyloxy group", "C3-8 cycloalkylthio group", "C3-8 cycloalkylsulfinyl group", or "C3-8 cycloalkylsulfonyl group" in X The above substituents include halogeno groups such as fluoro group, chloro group, bromo group and iodo group; methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, s-butyl group and i. C1-6 alkyl groups such as -butyl group, t-butyl group, n-pentyl group, n-hexyl group; chloromethyl group, chloroethyl group, trifluoromethyl group, 1,2-dichloro-n-propyl group, 1 C1-6 haloalkyl groups such as −fluoro-n-butyl group; methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, s-butoxy group, i-butoxy group, t-butoxy group C1-6 alkoxy groups such as 2-chloro-n-propoxy group, 2,3-dichlorobutoxy group, C1-6 haloalkoxy group such as trifluoromethoxy group; or cyano group; are preferable.

In the present invention, as X, a halogeno group, a halogeno group-substituted or unsubstituted C1-6 alkyl group, or a halogeno group-substituted or unsubstituted C1-6 alkoxy group is preferable.

The "C1-6 alkyl group substituted with a halogeno group" in X includes a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, and a 2,2,2,1,1-pentafluoroethyl group. And so on.
Examples of the "halogeno-substituted C1 to 6 alkoxy groups" in X include a difluoromethoxy group, a trifluoromethoxy group, a 2,2-difluoroethoxy group, a 2,2,2-trifluoroethoxy group, and 2,2,1. Examples thereof include 1-tetrafluoroethoxy group and 2,2,2,1,1-pentafluoroethoxy group.

[Q ¹ ]
In formula (I), Q ¹ represents a substituted or unsubstituted 5-membered heterocyclylene group.
The "5-membered heterocyclylene group" in Q ^1, consisting of 5-membered ring containing a nitrogen atom, 1, 2 is selected from the group consisting of oxygen and sulfur atoms, or three heteroatoms as member atoms in the ring It is a divalent group. When there are two or more heteroatoms, they may be the same or different.

The 5-membered heterocyclylene group includes a pyrrolylene group, a furylene group, a thienylene group, an imidazolylene group, a pyrazolylene group, an oxazolylene group, an isoxazolylene group, a thiazolylene group, an isothiazolylen group, a triazolylen group (1,2,4-triazolylen group, or 1). , 2,3-Triazolylen group), thiadiazolilen group (1,3,4-thiadiazolilen group, 1,2,5-thiadiazolilen group, 1,2,3-thiadiazolilen group, or 1,2,4-thiadiazolilen group) Oxadiazolylene group (1,3,4-oxadiazolylene group, 1,2,5-oxadiazolylene group, 1,2,3-oxadiazolylene group, or 1,2,4-oxadiazolylene group) And so on.
In the present invention, Q ¹ is preferably a substituted or unsubstituted triazolylen group.

The substituent on "5-membered heterocyclylene group" in Q ^1, fluoro group, chloro group, bromo group, a halogeno group such as iodo groups; methyl, ethyl, n- propyl, i- propyl, C1-6 alkyl groups such as n-butyl group, s-butyl group, i-butyl group, t-butyl group, n-pentyl group, n-hexyl group; chloromethyl group, chloroethyl group, trifluoromethyl group, 1 , 2-Dichloro-n-propyl group, 1-fluoro-n-butyl group and other C1-6 haloalkyl groups; methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, s-butoxy C1-6 alkoxy groups such as groups, i-butoxy groups, t-butoxy groups; C1-6 haloalkoxy groups such as 2-chloro-n-propoxy group, 2,3-dichlorobutoxy group, trifluoromethoxy group; phenyl Group; "Penyl group substituted with halogeno group, C1-6 haloalkyl group, or C1-6 haloalkoxy group" such as 4-chlorophenyl group, 4-trifluoromethylphenyl group, 4-trifluoromethoxyphenyl group; Alternatively, a cyano group is preferable.

[A]
A represents a substituted or unsubstituted C1-2 alkylene group.
Examples of the "C1-2 alkylene group" in A include a methylene group and a dimethylene group.
As the substituent on the "C1-2 alkylene group", a halogeno group such as a fluoro group, a chloro group, a bromo group and an iodo group; a methyl group, an ethyl group, an n-propyl group, an i-propyl group and an n-butyl group. , S-butyl group, i-butyl group, t-butyl group and other C1-6 alkyl groups; or chloromethyl group, chloroethyl group, trifluoromethyl group, 1,2-dichloro-n-propyl group, 1-fluoro C1-6 haloalkyl groups such as the -n-butyl group are preferred.

[Y ¹ , Y ² , ^Ra ]
Y ¹ represents a nitrogen atom or ^a group represented by ^{CR a, and Y 2} represents a nitrogen atom or ^a group represented by CR a. R ^a each independently represent a hydrogen atom, a halogeno group or a substituted or unsubstituted C1~6 alkyl group.
Specific examples of the "halogeno group" or "C1-6 alkyl" in ^{Ra can be the same as those exemplified in X.}

[Q ² ]
Q ² represents a substituted or unsubstituted 6-membered heteroaryl group.
The "6-membered heteroaryl group" in Q ^2, nitrogen atoms, aromatic 6-membered ring containing an oxygen atom and 1, 2, 3 or 4 heteroatoms selected from the group consisting of a sulfur atom as a constituent atom of the ring It is a monovalent group consisting of. When there are two or more heteroatoms, they may be the same or different. Examples of the 6-membered heteroaryl group include a pyridyl group, a pyrazinyl group, a pyrimidinyl group, a pyridadinyl group, a triazinyl group and the like.

The substituent on "6-membered heteroaryl group" in Q ^2, fluoro group, chloro group, bromo group, a halogeno group such as iodo groups; methyl, ethyl, n- propyl, i- propyl radical, n C1-6 alkyl groups such as -butyl group, s-butyl group, i-butyl group, t-butyl group, n-pentyl group, n-hexyl group; chloromethyl group, chloroethyl group, trifluoromethyl group, 1, C1-6 haloalkyl groups such as 2-dichloro-n-propyl group and 1-fluoro-n-butyl group; hydroxyl group; methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, s- C1-6 alkoxy groups such as butoxy group, i-butoxy group, t-butoxy group; C1-6 haloalkoxy groups such as 2-chloro-n-propoxy group, 2,3-dichlorobutoxy group, trifluoromethoxy group; Phenyl group; "phenyl group substituted with halogeno group, C1-6 haloalkyl group, or C1-6 haloalkoxy group" such as 4-chlorophenyl group, 4-trifluoromethylphenyl group, 4-trifluoromethoxyphenyl group. ; Or a cyano group is preferred.

The azinylazole compound of the present invention is not particularly limited depending on the production method thereof. For example, the azinylazole compound of the present invention (hereinafter, may be referred to as “the compound of the present invention”) can be obtained by a procedure described in Examples and the like using a known reaction.

The compound of the present invention is excellent in controlling harmful organisms such as various agricultural pests and mites that affect the growth of plants.
In addition, the compound of the present invention is a highly safe substance because it causes less phytotoxicity to crops and has low toxicity to fish and warm-blooded animals. Therefore, it is useful as an active ingredient of insecticides or acaricides.
Furthermore, in recent years, resistance to various existing drugs has developed in many pests such as diamondback moth, planthopper, leafhopper, and aphid, causing a problem of insufficient efficacy of these drugs, and a drug effective against pests of resistant strains is desired. ing. The compound of the present invention exhibits an excellent control effect not only on sensitive strains but also on pests of various resistant strains and mites of acaricide-resistant strains.

The compound of the present invention is excellent in controlling ectoparasites and endoparasites that are harmful to humans and animals. In addition, it is a highly safe substance because it has low toxicity to fish and warm-blooded animals. Therefore, it is useful as an active ingredient of a control agent for ectoparasites and endoparasites.

In addition, the compound of the present invention is effective at all developmental stages of the organism to be controlled, and exhibits an excellent control effect on, for example, eggs such as mites and insects, nymphs, larvae, pupae, and adults.

[Pest control agents, insecticides or acaricides]
The pest control agent, or insecticide or acaricide of the present invention contains at least one selected from the compounds of the present invention as an active ingredient. The amount of the pest control agent of the present invention or the compound of the present invention contained in the insecticide or acaricide is not particularly limited as long as it shows the control effect of pests, agricultural pests or mites.

The pest control agent, insecticide or acaricide of the present invention includes grains; vegetables; root vegetables; potatoes; flowers; fruit trees; foliage plants, tea, coffee, cacao and other trees; grasses; Turbs; preferably used for plants such as cotton.
In application to plants, the pest control agent, or insecticide or acaricide of the present invention, includes leaves, stems, stalks, flowers, buds, fruits, seeds, sprouts, roots, stalks, stalks, shoots, shoots, cuttings, etc. It may be used for the site of.
In addition, the pest control agent, insecticide or acaricide of the present invention is not particularly limited depending on the species of the plant to which it is applied. Examples of plant species include original species, varieties, improved varieties, cultivars, mutants, hybrids, genetically modified organisms (GMOs) and the like.

The pest control agent of the present invention can be used for seed treatment, foliage spraying, soil application, water surface application and the like in order to control various agricultural pests and mites.

Specific examples of various agricultural pests and mites that can be controlled by the pest control agent of the present invention are shown below.

(1) Lepidoptera butterflies or moths (a) Arctiidae moths, such as the fall webworm (Hyphantria cunea) and mulberry moth (Lemyra imparilis);
(B) Bucculatricidae moths, such as Bucculatrix pyrivorella;
(C) The family Carposinidae, for example, Carposina sasakii;
(D) Moths of the Crambidae family, such as the genus Diaphania spp., Diaphania indica, Diaphania nitidalis; eg, Ostrinia spp. , Awanomeiga (Ostrinia furnacalis), European cornballer (Ostrinia nubilalis), Azukinomeiga (Ostrinia scapulalis); Diatraea grandiosella), Kwanomeiga (Glyphodes pyloalis), Hymadalanomeiga (Hellula undalis), Shibatuga (Parapediasia teterrella);
(E) Moths of the family Twirler moth (Gelechiidae), such as caterpillar (Helcystogramma triannulella), cotton bollworm (Pectinophora gossypiella), potato moth (Phthorimaea operculella), and angoumois grain moth (Sitotroga cerealella);
(F) Moths of the Geometridae family, such as Artemisia selenaria;
(G) Moths of the family Chrysomelidae (Gracillariidae), such as Caloptilia theivora, Phyllocnistis citrella, Phyllonorycter ringoniella;
(H) Skippers (Hesperiidae) butterflies, such as Parnara guttata;
(I) Lappet moth (Lasiocampidae) moth, for example Lackey moth (Malacosoma neustria); (j) Tussock moth (Lymantriidae) moth, for example Lymantria spp. (Lymantria monacha); Others, Chadokuga (Euproctis pseudoconspersa), Himeshiromondokuga (Orgyia thyellina);

(K) Moths of the family Lyonetiidae, such as the genus Lyonetia spp., Lyonetia clerkella, Lyonetia prunifoliella malinella;
(L) Moths of the family Noctuidae, for example, Spodoptera spp., Spodoptera depravata, Southern army worm (Spodoptera eridania), Spodoptera exigua, Fall armyworm Spodoptera exigua, Fall armyworm. ), African Noctuidae (Spodoptera littoralis), Hasmon Noctuidae (Spodoptera litura); For example, Autographa spp., Gamma Kinuwaba (Autographa gamma), Tamanagin Uwaba (Autographa nigrisigna); Noctuidae (Agrotis ipsilon), Noctuidae (Agrotis segetum); For example, Helicoverpa spp., Helicoverpa armigera, Helicoverpa assulta, Cotton ball worm (Helicoverpa zea); Heliothis spp., Heliothis armigera, Heliothis virescens; Others, Aedia leucomelas, Ctenoplusia agnata, Eudocima tyran Mamestra brassicae), Awayoto (Mythimna separata), Futaobikoyaga (Naranga aenescens), Matsukiriga (Panolis japonica), Nisetama nayaga (Peridroma saucia), Soybean looper (Pseudoplusia includens), Irakusagin uwaba (Tricho)
(M) Moths of the Tuft moth family (Nolidae), such as Earias insulana;
(N) Pieridae (Pieridae) butterflies, such as the large white butterfly (Pieris brassicae) and the pieris (Pieris rapae crucivora) of the genus Pieris spp.
(O) Plutellidae moths, such as the Acrolepiopsis spp., Acrolepiopsis sapporensis, Acrolepiopsis suzukiella; and other diamondback moths (Plutella xylostella);
(P) Pyralidae moths, such as Cadra cautella, Elasmopalpus lignosellus, Etiella zinckenella, Greater wax moth;
(Q) Moths of the family Sphingidae, such as the Manduca spp. Tomato hornworm (Manduca quinquemaculata), Tobacco hornworm (Manduca sexta);

(R) Moths of the family Stahtmopodidae, such as the Stahmopoda masinissa;
(S) Moths of the family Tineidae, such as Tinea translucens;
(T) Moths of the Tortrix moth family, such as the Adoxophyes spp., Adoxophyes honmai, Adoxophyes orana; for example, the Archips spp. ), Ringomonhamaki (Archips breviplicanus), Midarekakumonhamaki (Archips fuscocupreanus); Others, Tohinoshintomehamaki (Choristoneura fumiferana), Kodriinga (Cydia pomonella), Grape Hosohamaki (Eupoecilia ambiguella) ), Chahamaki (Homona magnanima), Mameshiniga (Leguminivora glycinivorella), Hosobahimehamaki (Lobesia botrana), Mamehimesayamushiga (Matsumuraeses phaseoli), Tobihamaki (Pandemis heparana), Tenguhamaki (Sparganothis pill)
(U) Moths of the Ermine family (Yponomeutidae), such as the apple fruit moth (Argyresthia conjugella).

(2) Thripidae (Thysanoptera) pests (a) Thripidae (Phlaeothripidae), for example, Thripidae (Ponticulothrips diospyrosi);
(B) Thripidae, for example Frankliniella spp., Thripidae thripidae, Frankliniella occidentalis; for example, Thrips spp. Thrips palmi, Thrips tabaci; Others, Thripidae (Heliothrips haemorrhoidalis), Thripidae (Scirtothrips dorsalis).

(3) Pests of the order Hemiptera (A) Auchenorrhyncha
(A) Delphacidae, for example, Laodelphax striatella, Nilaparvata lugens, Perkinsiella saccharicida, Sogatella furcifera.

(B) Auchenorrhyncha
(A) Leafhoppers (Cicadellidae), for example, Empoasca spp., Leafhoppers (Empoasca fabae), Leafhoppers (Empoasca nipponica), Chanomidorihimeyokobai (Empoasca onukii), Maeno Leafhopper (Empoasca sakaii); Others, Leafhopper (Arboridia apicalis), Empoasca (Balclutha saltuella), Leafhopper (Epiacanthus stramineus), Leafhopper (Macrosteles striifrons) ..

(C) Heteroptera
(A) Of the family Riptortus pedestrianis (Alydidae), for example, Riptortus clavatus;
(B) Of the leaf-footed bug family (Coreidae), for example, the stink bug (Cletus punctiger), the spider stink bug (Leptocorisa chinensis);
(C) Of the family Lygaeidae, for example, Chinch bug (Blissus leucopterus), Cavelerius saccharivorus, Calabash serrata (Togo hemipterus);
(D) Of the family Hemiptera (Miridae), for example, black kite bug (Halticus insularis), sabiirokasumi turtle (Lygus lineolaris), cotton free hopper (Psuedatomoscelis seriatus), nagamugi lygus (Stenodema sibiricum), lygus lygus (Stenodema sibiricum) ), Rice Hosomidori Kasumi turtle (Trigonotylus caelestialium);

(E) Of the stink bug family (Pentatomidae), for example, of the genus Nezara (Nezara spp.), Of the stink bug (Nezara antennata), of the stink bug (Nezara viridula); , Stink bug (Eysarcoris aeneus), Stink bug (Eysarcoris lewisi), Stink bug (Eysarcoris ventralis), Others, Stink bug (Dolycoris baccarum), Stink bug (Dolycoris baccarum), Stink bug (Dolycoris baccarum) Halyomorpha halys), stink bug (Piezodorus hybneri), stink bug (Plautia crossota), stink bug (Scotinophora lurida);
(F) Of the family Pyrrhocoridae, for example, the red bug (Dysdercus cingulatus);
(G) Of the leaf-footed bug family (Rhopalidae), for example, the leaf-footed bug (Rhopalus msculatus);
(H) Of the family Buprestidae (Scutelleridae), for example, the wheat arma custos (Eurygaster integriceps);
(I) Tingidae, for example, Stephanitis nashi.

(D) Sternorrhyncha
(A) Adelgidae, for example, Larch aphid (Adelges laricis);
(B) Whitefly family (Aleyrodidae) For example, Silverleaf whitefly (Bemisia argentifolii), Tobacco whitefly (Bemisia tabaci) of the genus Bemisia (Bemisia spp.); Other whitefly (Aleurocanthus spiniferus), Whitefly (Di) citri), Whitefly (Trialeurodes vaporariorum);
(C) Aphididae, for example, Aphis spp., Aphis craccivora, Aphis fabae, Aphis forbesi, Aphis gossypii. , European apple aphid (Aphis pomi), chicken aphid (Aphis sambuci), snowy aphid (Aphis spiraecola); for example, corn aphid (Rhopalosiphum maidis), wheat aphid (Rhopalosiphum maidis), wheat aphid (Rhopalosiphum maidis) For example, the genus Aphididae (Dysaphis spp.), Aphididae (Dysaphis plantaginea), Aphididae (Dysaphis radicola); for example, the genus Macrosiphum spp. (Macrosiphum euphorbiae); for example, of the genus Myzus spp., Myzus cerasi, Myzus persicae, Myzus varians; pisum), potato aphid (Aulacorthum solani), wheat aphid (Brachycaudus helichrysi), daikon aphid (Brevicoryne brassicae), strawberry aphid (Chaetosiphon fragaefolii), peach aphid (Chaetosiphon fragaefolii) , Fake aphid (Lipaphis erysimi), Aphididae (Megoura viciae), Aphididae (Metopolophium dirhodum), Lettuce aphid (Nasonovia ribis-nigri) Phorodon humuli, Schizaphis graminum, Sitobion avenae, Toxoptera aurantii;

(D) Coccidae, for example, Ceroplastes spp., Ceroplastes ceriferus, Ceroplastes rubens;
(E) Diaspididae, Pseudaulacaspis spp., Pseudaulacaspis pentagona, Pseudaulacaspis prunicola; for example, Unaspis spp. Of the scale insects (Unaspis euonymi), the scale insects (Unaspis yanonensis); and others, the scale insects (Aonidiella aurantii), the scale insects (Comstockaspis perniciosa), the scale insects (Fiorinia) );
(F) Of the scale insect family (Margarodidae), for example, Drosicha corpulenta, Icerya purchasi;
(G) Of the family Aphididae (Phylloxeridae), for example, the grape aphid (Viteus vitifolii);
(H) Pseudococcidae, for example, Planococcus spp., Planococcus citri, Planococcus kuraunhiae; Other, Phenacoccus sol , Pseudococcus comstocki;
(I) Psyllidae, eg, Psylla spp., Psylla mali, Psylla pyrisuga; and other Diaphorina citri.

(4) Pests of the suborder Polyphaga (a) Anobiidae, for example, Lasioderma serricorne;
(B) Attelabidae, for example, Byctiscus betulae, Rhynchites heros;
(C) Lyctus brunneus of the family Lyctus brunneus;
(D) Of the family Cylas formicarius, for example, Cylas formicarius;
(E) Of the jewel beetle family (Buprestidae), for example, the jewel beetle (Agrilus sinuatus);
(F) Cerambycidae, for example, Anoplophora malasiaca, Monocohamus alternatus, Psacothea hilaris, Xylotrechus pyrrhoderus;
(G) Chrysomelidae, eg, Bruchus spp., Bruchus pisorum, Broad bean weevils (Bruchus rufimanus); eg, Diabrotica spp., Northern corn. Root worm (Diabrotica barberi), Southern corn root worm (Diabrotica undecimpunctata), Western corn root worm (Diabrotica virgifera); ); Others, Aulacophora femoralis, Callosobruchus chinensis, Cassida nebulosa, Chaetocnema concinna, Colorado leaf beetle (Leptinotarsa decemlineata), Inekubihosohamushi (Leptinotarsa decemlineata) Nagasnetobi beetle (Psylliodes angusticollis);

(H) Ladybugs (Coccinellidae), for example, Epilacna spp., Mexican bean beetle (Epilachna varivestis), Henosepilachna vigintioctopunctata;
(I) Curculionidae, for example, Anthonomus spp., Anthonomus grandis, Anthonomus pomorum; for example, Sitophilus spp. , Granary Weevils (Sitophilus granarius), Sitophilus zeamais; Others, Weevils (Echinocnemus squameus), Weevils (Euscepes postfasciatus), Weevils (Hylobius abietis) Lissohoptrus oryzophilus), Sitophilus weevil (Otiorhynchus sulcatus), Red-spotted weevil (Sitona lineatus), Sitophilus weevil (Sphenophorus venatus);
(J) Click beetles (Elateridae), for example, Melanotus spp., Melanotus fortnumi, Melanotus tamsuyensis;
(K) Sap beetle (Nitidulidae), for example, Sap beetle (Epuraea domina);
(L) Scarabaeidae, for example, Anomala spp., Anomala cuprea, Anomala rufocuprea; Others, Gametis jucunda, Gametis jucunda ), Nagachakogane (Heptophylla picea), European scarabaeoidea (Melolontha melolontha), Mamekogane (Popillia japonica);
(M) Of the bark beetle family (Scolytidae), for example, the spruce bark (Ips typographus);
(N) Staphylinidae, for example, Paederus fuscipes;
(O) Tenebrionidae, for example, Tenebrio molitor, Red flour beetle (Tribolium castaneum);
(P) Of the family Red flour beetle (Trogossitidae), for example, the red flour beetle (Tenebroides mauritanicus).

(5) Diptera pests (A) Brachycera
(A) Agromyzidae, for example, Agromyzidae (Liriomyza spp.), Agromyzidae (Liriomyza bryoniae), Agromyzidae (Liriomyza chinensis), Tomato leafminer (Liriomyza sativae), Agromyzidae (Liriomyza sativae), Agromyzidae (Liriomyza sativae) Others, Agromyzidae (Chromatomyia horticola), Agromyzidae (Agromyza oryzae);
(B) Anthomyiidae, eg, Delia spp., Delia platura, Delia radicum; and other sugar beet, Pegomya cunicularia;
(C) Drosophilidae, for example, Drosophila spp., Drosophila melanogaster, Drosophila suzukii;
(D) Ephydridae, for example, Hydrellia griseola;
(E) From the family Psilidae, for example, the carrot fly (Psila rosae);
(F) Fruit flies (Tephritidae), for example, Bactrocera spp., Bactrocera cucurbitae, Bactrocera dorsalis; for example, Rhagoletis spp. Rhagoletis cerasi), lingo fly (Rhagoletis pomonella); other, Chichukai mibae (Ceratitis capitata), olive mibae (Dacus oleae).

(B) Nematocera
(A) Cecidomyiidae, for example, Soybean Cecidomyiidae, Sorghum sorghicola, Hessian fly (Mayetiola destructor), Mugia caterpillar (Sitodiplosis mosellana).

(6) Orthoptera pests (a) Acrididae, for example, Schistocerca spp., American locusts (Schistocerca americana), Sabactobibatta (Schistocerca gregaria); Australian locusts (Chortoicetes terminifera), Moroccan locusts (Dociostaurus maroccanus), Tonosama locusts (Locusta migratoria), Brown locusts (Locustana pardalina), Akato locusts (Nomadacris septemfasciata), Kobaneinago (Oxya yezoensis)
(B) Cricket family (Gryllidae), such as European house cricket (Acheta domestica), cricket (Teleogryllus emma);
(C) Mole cricket (Gryllotalpidae), for example, mole cricket (Gryllotalpa orientalis);
(D) Of the Bush cricket family (Tettigoniidae), for example, Tachycines asynamorus.

(7) Mites (Acari)
(A) Acaridida of the order Astigmata
(A) Acaridae mites, such as Rhizoglyphus spp., Rhizoglyphus echinopus, Rhizoglyphus robini; for example, Tyrophagus spp. (Tyrophagus neiswanderi), Okenagakonadani (Tyrophagus perniciosus), Kenagakonadani (Tyrophagus putrescentiae), Horensokenagakonadani (Tyrophagus similis);

(B) Prostigmata prostigmata (Actinedida)
(A) Spider mite (Tetranychidae) mites, such as Bryobia spp., Clover mite (Bryobia praetiosa), fake clover mite (Bryobia rubrioculus); for example, Eotetranychus spp. , Eotetranychus asiaticus, Anzu spider mite (Eotetranychus boreus), Eotetranychus celtis, Michinoku spider mite (Eotetranychus geniculatus), Miyake spider mite (Eotetranychus geniculatus), Miyake spider mite (Eotetranychus kankitus) (Eotetranychus smithi), Suginami spider mite (Eotetranychus suginamensis), walnut spider mite (Eotetranychus uncatus); Mango spider mite (Oligonychus mangiferus), sugar cane spider mite (Oligonychus orthius), avocado spider mite (Oligonychus perseae), Ezosugi spider mite (Oligonychus pustulosus), rice spider mite (Oligonychus shinkajii) Panonychus citri, Panonychus mori, Panonychus ulmi; for example, Tetranychus spp., Tetranychus cinnabarinus, Tetranychus cinnabarinus, Tetranychus cinnabarinus, Tetranychus cinnabarinus, Tetranychus cinnabarinus kanzawai), Asinowa spider mite (T etranychus ludeni), Quercus crispula (Tetranychus quercivorus), Sagami spider mite (Tetranychus phaselus), Nami spider mite (Tetranychus urticae), Oto spider mite (Tetranychus viennensis); (Aponychus firmianae); for example, Tetranychus spp., Tetranychus akitanus, Tetranychus pusillus; for example, Shizotetranychus spp. Shizotetranychus longus, Shizotetranychus miscanthi, Shizotetranychus recki, Shizotetranychus schizopus; ;

(B) Mites of the family Tenuipalpidae, such as Brevipalpus spp., Brevipalpus lewisi, Brevipalpus obovatus, Brevipalpus phoenicis, Brevipalpus phoenicis, Brevipalpus phoenicis. russulus), Brevipalpus californicus; for example, Tenuipalpus spp., Tenuipalpus pacificus, Tenuipalpus zhizhilashviliae; Other, pineapple zhizhilashviliae;
(C) Eriophyidae mites, such as Aceria spp., Aceria diospyri, Aceria ficus, Aceria japonica, Aceria kuko, carnation. Aceria paradianthi, Aceria tiyingi, Aceria tulipae, Aceria zoysiea; for example, Eriophyes spp., Eriophyes chibaensis, Eriophyes chibaensis emarginatae); for example, Tomato sabi mite (Aculops lycopersici), Mikan sabi mite (Aculops pelekassi); schlechtendali; Others, Acaphylla theavagrans, Calacarus carinatus, Colomerus vitis, Calepirimerus vitis, Epitrimerus pyri, Epitrimerus pyrai podocarpi), Ryukyu mites (Phyllocotruta citri);
(D) Tarsonemidae mites, such as Tarsonemus spp., Tarsonemus bilobatus, Tarsonemus waitei; and other cyclamen tarsonemidae (Phytonemus pallidus) and polyphagotarsone. );
(E) Penthaleidae mites, such as Penthaleus spp., Penthaleus erythrocephalus, and Penthaleus major.

The pest control agents of the present invention are other active ingredients such as fungicides, insecticides / acaricides, nematode pesticides, soil pesticides; plant growth regulators, synergists, fertilizers, soil conditioners, for animals. It may be mixed or used in combination with feed or the like.
The combination of the compound of the present invention and another active ingredient can be expected to have a synergistic effect on insecticidal, acaricidal, and nematode activity. The synergistic effect can be confirmed by Colby's formula (Colby.SR; Calculating Synergistic and Antagonistic Responses of Herbicide Combinations; Weeds 15, pp. 20-22, 1967) according to a conventional method.

Specific examples of insecticides / acaricides, nematodes, soil pesticides, anthelmintics and the like that can be mixed or used in combination with the pest control agent of the present invention are shown below.

(1) Acetylcholinesterase inhibitor:
(A) Carbamates: Aranicalb, Aldicarb, Bengiocarb, Benfracarb, Butocarboxim, Butoxycarboxim, Carbaryl, Carbofuran, Carbosulfan, Ethiophenacarb, Phenoccarb, Formetanate, Frathiocarb, Isoprocarb, Methiocarb, Methomyl, Oxamil, Pyrimicarb, Propoxal. Thiodicarb, thiofanox, triazamate, trimetacarb, XMC, xylylcarb, phenothiocarb, MIPC, MPMC, MTMC, aldicarb, alixcarb, aminocarb, butocarboxim, chlorocarb, metam sodium, promecarb;

(B) Organophosphorus: acetylate, azamethifos, azinephos-ethyl, azinephos-methyl, kazusaphos, chlorethoxyphos, chlorpyrifos, chlormefos, chlorpyrifos, chlorpyrifos-methyl, kumaphos, cyanophos, demethon-S-methyl, diazinone, Dichlorpyrifos / DDVP, Dimethoate, Dimethoate, Dimethylbinphos, Disulfoton, EPN, Ethion, Etoprophos, Famfur, Fenamiphos, Fenitrothione, Fention, Hostiazeto, Heptenophos, Imiciaphos, Isophenphos, Isocarbhos, Isoxathione, Malathion, Mecarbam Monochrometophos, Naredo, Ometoate, Oxydimetone-Methyl, Palatin, Palatin-Methyl, Fentate, Holate, Hosalon, Hosmet, Phosphamide, Hoxim, Pyrimiphos-Methyl, Prophenofus, Propetamphos, Prothiophos, Pyraclophos, Pyridafenthion, Kinalphos, Sulfonep, Temefos Temefos, Telbuphos, Tetrachlorpyrifos, Thiometon, Triazophos, Trichlorfon, Bamidethione, Bromophos-Ethyl, BRP, Carbophenothione, Cyanophenphos, Demeton-S-Methylsulfosone, Dialiphos, Diclofenthion, Dioxabenzophos, Etrimphos, Fensulfothione , Flupyrifos, Honophos, Hormothione, Hosmethyran, Isazophos, Iodophenphos, Metrifos, Pyrimiphos-Ethyl, Phosphorcarb, Propaphos, Protoate, Sulfrophos.

(2) GABA-Operating Chloride Ion Channel Antagonists: Acetoprol, Chlordane, Endosulfan, Ethiprol, Fipronil, Pyrafluprol, Pyriprol, Canfechlor, Heptachlor, Dienochlor.
(3) Sodium channel modulators: acrinathrin, d-cis-trans-allethrin, d-trans-allethrin, bifentrin, bioallethrin, bioalethrin S-cyclopentyl isomer, bioresmethrin, cycloprothrin, cypermethrin, beta-cypermethrin, cypermethrin, lambda- Cypermethrin, gamma-cypermethrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cypermethrin [(1R) -trans isomer], deltamethrin, empentrin [(EZ)-( 1R)-isomer], esphenvalerate, etofenprox, phenpropathrin, fenvalerate, flucitrinate, flumethrin, tau-fluvalinate, halphenprox, imiprithrin, cadesrin, permethrin, phenothrin [(1R) -trans Heterogeneous], permethrin, pyrethrum, lesmethrin, cypermethrin, tefluthrin, tetramethrin [(1R) -isomer], tralomethrin, transfluthrin, allethrin, pyrethrin, pyrethrin I, permethrin II, profluthrin, dimefluthrin, bioetanomethrin Permethrin, transpermethrin, fenfluthrin, fenpyritrin, flubrocitrinate, flufenprox, methfurthrin, protrifenbut, pyresmethrin, terraretrin.

(4) Nicotinic acetylcholine receptor agonists: acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazine, thiacloprid, thiamethoxam, sulfoxaflor, nicotine, flupyradiflon, flupyrimin.
(5) Nicotinic acetylcholine receptor allosteric modulator: spinetram, spinosad.
(6) Chloride channel activator: abamectin, emamectin benzoate, repimectin, milbemectin, ivermectin, selamectin, dramectin, eprinomectin, moxidectin, milbemycin, milbemycin oxime, nemadetin.
(7) Juvenile hormone-like substances: hydroprene, quinoprene, methoprene, phenoxycarb, pyriproxyfen, diophenolan, epophenonan, triprene.
(8) Other non-specific inhibitors: methyl bromide, chloropicrin, sulfuryl fluoride, borax, liquor stone.
(9) Hemiptera selective feeding inhibitors: Fronicamid, Pymetrodin, Pyrifluquinazone.

(10) Mite growth inhibitors: clofentezine, difluorovidazine, hexitiazox, etoxazole.
(11) Microbial-derived insect mid-intestinal intestinal destructive agent: Bacillus thuringiensis subspecies Isla Elenshi, Bacillus thuringiensis subspecies Isla Elenshi, Bacillus thuringiensis subspecies Isawai, Bacillus thuringiensis subspecies Kurstaki, Bacillus thuringiensis subspecies Teneblionis, Bt Crop protein, Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb, Cry34Ab1 / Cry35Ab1.
(12) Mitochondrial ATP biosynthetic enzyme inhibitor: diafentiurone, azocyclotin, cyhexatin, fenbutatin oxide, propargite, tetradiphon.
(13) Oxidative phosphorylation decoupling agent: chlorfenapyr, sulfurlamin, DNOC, binapacryl, dinobutone, dinocup.
(14) Nicotinic Acetylcholine Receptor Channel Blocker: Bensultap, Cartap Hydrochloride, Neristoxin, Thiosultap-Sodium Salt, Thiocyclum.
(15) Chitin synthesis inhibitors: bistrifluron, chlorflubenzuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumron, lufenuron, novalron, nobiflumron, teflubenzuron, triflubenzuron, buprofezin, fluazuron.
(16) Diptera molting disturber: Cyromazine.
(17) Moulting hormone receptor agonists: chromaphenozide, halophenozide, methoxyphenozide, tebufenozide.
(18) Octopamine receptor agonists: Amitraz, Demiditraz, Chlordimeform.
(19) Mitochondrial electron transport chain complex III inhibitor: acequinosyl, fluacripirim, hydramethylnon, biphenazate.
(20) Mitochondrial electron transport chain complex I inhibitor: phenazakin, phenpyroximate, pyrimidiphen, pyridaben, tebufenpyrado, tolfenpyrad, rotenone.

(21) Voltage-gated sodium channel blockers: indoxacarb, metaflumisone.
(22) Acetyl-CoA carboxylase inhibitors: spirodiclophen, spiromesiphen, spirotetramato, spiropidion.
(23) Mitochondrial electron transport chain complex IV inhibitor: aluminum phosphide, calcium phosphide, phosphine, zinc phosphide, cyanide.
(24) Mitochondrial electron transport chain complex II inhibitor: sienopyraphen, siflumethofen, piflubumid.
(25) Ryanodine receptor modulators: chloranthraniliprole, cyantraniliprole, flubendiamide, cyclaniliprole, tetraniliprole.
(26) Mixed Function Oxidase Inhibitor Compound: Piperonyl butoxide.
(27) Latrophilin receptor agonists: depsipeptide, cyclic depsipeptide, 24-membered cyclic depsipeptide, modepside.
(28) Other agents (mechanism of action unknown): asinonapill, azadilactin, benzoximate, bromopropirate, quinomethionate, cryolite, dicoform, pyridalyl, bencrothias, sulfur, amide flumet, 1,3-dichloropropene, DCIP Phenisobromolate, benzomate, metaldehyde, chlorbenzylate, clothiazoben, disicranyl, phenoxacrim, fentrifanyl, flubenzimine, flufenazine, gossiplua, japonilua, metoxadiazone, petroleum, sodium oleate, tetrasul, triarasen, afidopyropen ), Fromotkin, flufiprole, fluensulphon, meperfluthrin, tetramethylfluthrin, traropyryl, methylneodecanamide, flularanel, afoxolanel, fluxametamide, 5- [5- (3,5-dichlorophenyl) -5-trifluoromethyl- 4,5-Dihydroisoxazole-3-yl] -2- (1H-1,2,4-triazole-1-yl) benzonitrile (CAS: 943137-49-3), brofuranilide, triflumesopyrim, dichloromezo Chiaz, oxazosulfyl, other metaldehydes, ticropyrazoflor.

(29) Anthelmintic:
(A) Benzimidazole system: fenbendazole, albendazole, triclabendazole, oxybendazole, mebendazole, oxfendazole, perbendazole, flubendazole, fevantel, netobimin, thiophanate, thiabendazole, cambendazole;
(B) Salicylanilide system: closantel, oxyclozanide, lafoxanide, niclosamide;
(C) Substituted phenolic system: nitroxynyl, nitroscanate;
(D) Pyrimidines: Pyrantel, Morantel;
(E) Imidazothiazole type: levamisole, tetramisole;
(F) Tetrahydropyrimidines: Praziquantel, Epsiprantel;
(G) Other anthelmintics: cyclodiene, liania, chlorthrone, metronidazole, demiditraz, piperazine, diethylcarbamazine, dichlorophene, monepantel, tribendimidine, amidantel, thiacetalsamide, merolsamine, arsenamide.

Specific examples of the fungicide that can be mixed or used in combination with the pest control agent of the present invention are shown below.
(A) Nucleic Acid Synthesis and Metabolism Inhibitors (1) RNA polymerase I Inhibitors Benalaxil, Benalaxil M, Flaluxil, Metalaxil, Metalaxil M; Oxadixil;
(2) Adenosine deaminase inhibitors bupirimate, dimethilimol, etilimol.
(3) DNA / RNA biosynthesis inhibitor himexazole, octylineone.
(4) DNA topoisomerase type II inhibitor oxolinic acid.

(B) Cytoskeleton and motor protein inhibitors (1) β-tubulin polymerization inhibitors benomyl, carbendazim, fuberidazole, thiabendazole, thiophanate, thiophanate-methyl, dietophencarb, zoxamide,
Etaboxam.
(2) Other inhibitors Pencyclon. Full opicoride. Fenamacril, Metraphenone, Periodophenone.

(C) Respiratory Inhibitor (1) Complex I: NADH Oxidoreductase Inhibitor Diflumetrim, Torfenpyrado, Phenazakin.
(2) Complex II: Inhibitors of succinate dehydrogenase Benodanyl, flutranyl, mepronil; isofetamide; fluopyram; fenfram; carboxyne, oxycarboxyne; tifluzamide; benzobindiflupill, bixaphen, fluindapyl, fluxapyroxado, Flametopill, impilfluxam, isopyrazam, penflufen, penthiopyrado, sedaxan; isoflusiplum; pidiflumethophene; boscalide; pyraziflumid.
(3) Complex III: Inhibitor of cytochrome bc1 (ubiquinol oxidase) Qo site (cyt b gene) Azoxystrobin, spiderxistrovin, enoxastrobin, fluphenoxystrobin, picoxystrobin, pyraoxy Strobin; Mandestrobin; Pyracrostrobin, Pyrametstrobi, Triclopyricalve; Cresoximemethyl, Trifloxystrobin; Dimoxystrobin, Phenaminestrobin, Metominostrobin, Orisastrobin; Famoxadon; Fluoxastrobin; Fenamiden Pyriben carve.
(4) Complex III: Inhibitor of ubiquinone reductase Qi site Ciazofamide; amisulbrom; fenpicoxamide.
(5) Oxidative phosphorylation decoupling agent Binapacryl, Dinocup, Meptyldinocup; Fluazinum.
(6) Inhibitors of oxidative phosphorylation and ATP synthase Triphenyltin acetate, triphenyltin chloride, triphenyltin hydroxide.
(7) Inhibitor of ATP transport Sylthiofam.
(8) Complex III: Amethoctrazine, an inhibitor of ubiquinone reductase (Qo site, stigmaterin-binding subsite).

(D) Amino acid and protein synthesis inhibitors cyprodinyl, mepanipyrim, pyrimethanyl. Blasticidin S. Kasugamycin, kasugamycin hydrochloride, streptomycin. Oxytetracycline.

(E) Signal transduction inhibitors quinoxyphen, proquinazide. Fempicronyl, fludioxonyl. Crozoline, dimetacron, iprodion, procymidone, bin clozoline.

(F) Agents that inhibit lipid biosynthesis or transport / structure or function of cell membranes Edifenphos, iprobenphos, pyrazophos; isoprothiolane.
Biphenyl, chloroneb, dichloran, quintozen, technazen, turquophosmethyl; etridiazole. Iodocarb, propamocarb, propamocarb hydrochloride, prothiocarb. Natamycin. Oxatiapiproline.

(G) Cell membrane sterol biosynthesis (inhibitor)
(1) Inhibitor of demethylase (erg11 / cyp51) at position C14 in sterol biosynthesis Triphorin; pyriphenox, pyrisoxazole; phenalimol, nuarimol; imazalyl, oxpoconazole, pefrazoate, prochloraz, triflumizole; azaconazole, bitertanol, Bromconazole, cyproconazole, diphenoconazole, diniconazole, epoxyconazole, etaconazole, fenbuconazole, flukinconazole, flucilazole, flutriahole, hexaconazole, imibenconazole, ipconazole, metconazole, microbutanyl, penconazole, propico Nazole, simeconazole, tebuconazole, tetraconazole, triazimefone, triazimenol, triticonazole, prothioconazole.
(2) Inhibitors of Δ14 reductase and Δ8 → Δ7-isomerase (erg24, erg2) in sterol biosynthesis Aldimorph, dodemorph, dodemorph acetate, fenpropimorph, tridemorph; fenpropidine, piperarin; spiroxamine.
(3) Inhibitors of 3-keto reductase (erg27) in C4 demethylation of sterol biosynthesis system Fenhexamide and fenpyrazamine.
(4) Inhibitors of sterol biosynthetic squalene epoxide (erg1) Pyrybutycarb, naftifine, terbinafine.

(H) Inhibitor of cell wall biosynthesis Polyoxin. Dimethmorph, Fullmorph, Pirimorph; Bench Avaricarb, Iprovaricarb, Variphenalate; Mandipropamide.

(I) Inhibitor of melanin synthesis in cell wall Fusalide; pyrokyron; tricyclazole. Calpropamide, diclosimet, phenoxanyl. Torpro Calve.

(P) Host plant resistance inducer acibenzolar S-methyl; probenazole; thiazinyl, isothianil. Laminarin. Reynoutria sachalinensis extract. Bacillus mycoides isolate J. Josetil, phosphorous acid and salts, Josetil calcium, Josetil sodium.

(U) Agents of unknown mechanism Simoxanil; tecrophthalam; triazoxide; flusulfamide; dichromedin; siflufenamide; dodine, dodine free base; fluthianyl; ferimzone; tebuflokin; picarbutrazox; validamycin.
Fluoxapyrroline, florylpicoxamide, fluopimomid, ipfluphenokin methyltetraprol, pyridacromethyl, pyrapropone, aminopyriphen, diclobenazox, ipfentrifluconazole, mefentrifluconazole, quinofmerin, dipimethitron.

(M) Agents exhibiting multi-point contact activity Copper (various salts), basic copper sulfate, Bordeaux solution, copper hydroxide, copper naphthalate, copper oxychloride, copper sulfate, copper oxide, oxine copper; sulfur, lime sulfur Agents; Farbam, Manzeb, Manneb, Methylam, Propineb, Thiuram, Thiazol Zinc, Dineb, Diram; Captan, Captahole, Holpet; Chlorotalonyl; Diclofluanide, Trillfluanide; Alvesylate; anilazine; dithianone; quinomethionate; fluorimide; metasulfocarb.

Specific examples of plant growth regulators that can be mixed or used in combination with the pest control agent of the present invention are shown below.
1-Methylcyclopropene, 2,3,5-triiodobenzoic acid, IAA, IBA, MCPA, MCPB, 4-CPA, 5-aminoleverellinate, 6-benzylaminopurine, abscisic acid, abigricin hydrochloride, ansimi Dole, butruarline, calcium carbonate, calcium chloride, calcium formate, calcium peroxide, lime sulfur, calcium sulfate, chlormecoat chloride, chloroprofem, choline chloride, cloprop, cyanamide, cyclanilide, daminozide, decyl alcohol, gibberellin , Dikeglack, dimethipine, diquat, etephone, ethiclocate, flumethrolin, fluluprimidol, holchlorphenuron, gibberellin A, gibberellin A3, himexazole, inabenfide, isoprothiolan, kinetin, maleic acid hydrazide, mefluidide, mepicot chloride Paclobutrazole, pendimethalin, prohexadione calcium, prohydrojasmon, pyraflufenethyl, syntophen, sodium 1-naphthalene acetate, sodium cyanate, streptomycin, tidiazulone, triapentenol, tribfoss, trinexapacethyl, Uniconazole P, 1-naphthylacetamide.

[Pest control agent]
The ectoparasite control agent of the present invention contains at least one selected from the compounds of the present invention as an active ingredient. The amount of the compound of the present invention contained in the ectoparasite control agent of the present invention is not particularly limited as long as it exhibits the ectoparasite control effect.

Host animals to be treated with the ectoparasite control agent of the present invention include pet animals such as dogs and cats; pet birds; livestock such as cows, horses, pigs and sheep; poultry; and other warm-blooded animals. be able to. Other examples include bees, stag beetles, and beetles.

The ectoparasite control agent of the present invention can be applied by a known veterinary method (topical, oral, parenteral or subcutaneous administration). The method is to administer it orally to animals by mixing tablets, capsules, feed, etc .; to administer it to animals by dipping solution, suppository, injection (intramuscular, subcutaneous, intravenous, intraperitoneal, etc.); oily or A method of locally administering an aqueous solution by spraying, pore-on, spot-on, etc .; Kneading an ectoparasite control agent into a resin, molding the kneaded product into an appropriate shape such as a collar or ear tag, and applying it to an animal. A method of wearing and locally administering; etc. can be mentioned.

Ectoparasites parasitize in and on host animals, especially warm-blooded animals. Specifically, it parasitizes the back, armpits, lower abdomen, inner crotch, etc. of the host animal and inhabits by obtaining nutrient sources such as blood and dandruff from the animal. Examples of ectoparasites include mites, lice, fleas, mosquitoes, stable flies, and flesh flies. Specific examples of ectoparasites that can be controlled by the ectoparasite control agent of the present invention are shown below.

(1) Mites (Acari)
Dermanyssidae mites, Macronyssidae mites, Laelapidae mites, Varroidae mites, Argasidae mites, Ixodidae mites, cucumber mites Insect-parasitic mites such as Psoroptidae mites, Sarcoptidae mites, Knemidokoptidae mites, Demodixidae Demodixidae mites, Trombiculidae mites, and mulberry mites. ..
(2) Lice (Phthiraptera)
Lice of the family Haematopinidae, lice of the family Linognathidae, mallophaga of the family Menoponidae, mallophaga of the family Philopteridae, mallophaga of the family Mammal chewing (Trichodectida).
(3) Flea eyes (Siphonaptera)
Human flea (Pulicidae) fleas, such as dog fleas (Ctenocephalides spp.), Dog fleas (Ctenocephalides canis), cat fleas (Ctenocephalides felis);
Fleas of the family Ceratophyllidae, fleas of the family Ceratophyllidae, fleas of the family Ceratophyllidae (Leptopsyllidae).
(4) Hemiptera.
(5) Diptera pests Culicidae mosquitoes, gnats Simuliidae gnats, Ceratopogonidae nukakas, Tabanidae abs, Muscidae flies, Glossinidae flies, Gnat flies, Hipboboscidae flies, Calliphoridae flies, Oestridae flies.

[Endoparasite control or extermination agent]
The endoparasite control or extermination agent of the present invention contains at least one selected from the compounds of the present invention as an active ingredient. The amount of the compound of the present invention contained in the endoparasite control or extermination agent of the present invention is not particularly limited as long as it shows the effect of controlling endoparasites.

The parasite that is the target of the endoparasite control or extermination agent of the present invention parasitizes in host animals, particularly warm-blooded animals and fish (endoparasites). Host animals for which the endoparasite control or extermination agent of the present invention is effective include humans, domestic mammals (eg, cows, horses, pigs, sheep, goats, etc.), experimental animals (eg, mice, rats, gerbils, etc.). , Pet animals (eg hamsters, guinea pigs, dogs, cats, horses, squirrels, rabbits, ferrets, etc.), wild and zoo mammals (monkeys, foxes, deer, buffalo, etc.), poultry (gerbils, ducks, chickens, quail, etc.) , Gacho, etc.), warm-blooded animals such as pet birds (such as pigeons, parrots, nine official birds, literary birds, inco, juushi pine, canary, etc.); or fish such as salmon, trout, and gerbil. By controlling and exterminating parasites, parasite-borne parasite diseases can be prevented or treated.

Examples of parasites to be controlled or exterminated include the following.
(1) Nematodes of the order Dioctophymatida (a) Nematodes of the family Dioctophymatidae, for example, Dioctophyma renale of the genus Dioctophyma spp.
(B) Kidneyworms of the Soboliphymatidae family, such as Soboliphyme abei and Soboliphyme baturini of the Soboliphyme spp.

(2) Nematodes of the order Trichocephalida (a) Trichinella spiralis of the Trichinellidae family, for example, Trichinella spiralis of the Trichinella spp. Species;
(B) Trichuridae trichuridae, for example, Trichuridae species, Capillaria annulata, Capillaria contorta, Liver hair nematodes (Capillaria contorta) Capillaria hepatica, Capillaria perforans, Capillaria plica, Capillaria suis; Trichuris spp., Trichuris vulpis, cattle Trichuris discolor, Trichuris ovis, Trichuris skrjabini, Trichuris suis.

(3) Nematodes of the order Rhabditida (Rhabditida) Nematodes of the family Rhabditida (Strongyloididae), for example, the genus Threadworm (Strongyloides spp.), Papillary nematodes (Strongyloides papillosus), cat feces Nematodes (Strongyloides planiceps), Pig manure nematodes (Strongyloides ransomi), Pig manure nematodes (Strongyloides suis), Feces nematodes (Strongyloides stercoralis), American cat manure nematodes (Strongyloides tumefaciens), Mouse manure nematodes (Strongyloides ratti) ..

(4) Strongylida nematodes Ancylostomatidae hookworms, such as Ancylostoma spp., Brazilian hookworm (Ancylostoma braziliense), dog hookworm (Ancylostoma caninum), and Zubini hookworm. (Ancylostoma duodenale), cat hookworm (Ancylostoma tubaeforme); Uncinaria stenocephala, narrow-headed hookworm (Uncinaria stenocephala); Bunostomum trigonocephalum).

(5) C. elegans of the order Strongylida (a) C. elegans of the family Angiostrongylidae, for example, Aelurostrongylus abstrusus of the genus Aelurostrongylus spp.; Angiostrongylus vasorum of the genus Angiostrongylus spp., Angiostrongylus cantonesis;
(B) Crenosomatidae nematodes, such as Crenosoma spp., Crenosoma aerophila, Crenosoma vulpis;
(C) Nematodes of the family Filaroididae, such as Filaroides spp., Filaroides hirthi, Filaroides osleri;
(D) Paragonimiasis of the family Paragonimiasis (Metastrongylidae), for example, Metastrongylus spp., Metastrongylus apri, Metastrongylus asymmetricus, Metastrongylus pudendectus (Metastrongylus asymmetricus) Metastrongylus pudendotectus), Metastrongylus salmi;
(E) Syngamidae beaks, such as Cyathostoma spp., Cyathostoma bronchialis; Syngamus spp., Scrijabin beaks (Syngamus spp.) Syngamus skrjabinomorpha), chicken beak (Syngamus trachea).

(6) C. elegans of the order Strongylida (a) C. elegans of the family Molineidae, for example, Nematodirus spp., Nematodirus filicollis, Nematodirus spa Tiger (Nematodirus spathiger);
(B) Nematodes of the family Dictyocaulidae (Dictyocaulus spp.), Dictyocaulus filaria, Dictyocaulus viviparus;
(C) Haemonchidae nematodes, such as Haemonchus contortus, Haemonchus contortus; Mecistocirrus spp., Mecistocirrus spp. (Mecistocirrus digitatus);
(D) Haemonchidae nematodes, such as Ostertagia ostertagi of the genus Ostertagia spp.;
(E) Nematodes of the family Heligmonellidae, such as the genus Nippostrongylus spp., Nippostrongylus braziliensis;
(F) Nematodes of the family Trichostrongylidae, for example, Trichostrongylus spp., Trichostrongylus axei, Trichostrongylus colubriformis. ), Trichostrongylus tenuis; Hyostrongylus spp., Hyostrongylus rubidus; Obeliscoides spp., Obeliscoides cuniculi ).

(7) C. elegans of the order Strongylida (a) C. elegans of the family Chabertiidae, for example, Chabertia ovina of the genus Chabertia spp.; Intestinal nodules. Insect genus (Oesophagostomum spp.), Intestinal nodule (pig) (Oesophagostomum brevicaudatum), Colombian intestinal nodule (Oesophagostomum columbianum), pig intestinal nodule (Oesophagostomum dentatum), intestinal nodule (pig) (Oesophagostomum georgianum) Oesophagostomum maplestonei, Oesophagostomum quadrispinulatum, Oesophagostomum radiatum, Oesophagostomum venulosum, Oesophagostomum venulosum, Oesophagostomum venulosum, Oesophagostomum venulosum
(B) Nematodes of the family Stephanuridae, eg, Stephanurus dentatus of the genus Stephanurus spp.;
(C) Strongylus vulgaris, for example, Strongylus spp., Strongylus asini, Strongylus edentatus, Strongylus equinus. , Strongylus vulgaris.

(8) Oxyurida nematodes Oxyuridae nematodes, such as the Enterobius spp., Enterobius anthropopitheci, Enterobius vermicularis; Oxyuris. Oxyuris equi of spp.); Passalurus ambiguus of the genus Passalurus spp.

(9) Ascaridida nematodes (a) Ascaridiidae nematodes, such as chicken roundworm species (Ascaridia spp.), Chicken roundworm (Ascaridia galli);
(B) Heterakidae nematodes, such as the Heterakis spp., Heterakis beramporia, Heterakis brevispiculum, and Heterakis gallinarum. , Heterakis pusilla, Heterakis putaustralis;
(C) Anisakidae nematodes, such as Anisakis simplex from the genus Anisakidae (Anisakis spp.);
(D) Ascarididae nematodes, such as roundworms (Ascaris spp.), Human roundworms (Ascaris lumbricoides), pig roundworms (Ascaris suum); Parascaria spp. (Parascaris equorum);
(E) Toxocara canis, Toxocara canis, Toxocara canis, Toxocara canisum, Toxocara vitulorum, nematodes of the Toxocara family (Toxocaridae), for example, Toxocara spp. ), Toxocara cati.

(10) Nematodes of the order Spirurida (a) Nematodes of the Onchocercidae family, for example, Brugia malayi and Brugia malayi of the genus Brugia spp. (Brugia pahangi), Brugia patei; Dipetalonema spp., Dipetalonema reconditum; Dirofilaria spp., Dirofilaria spp. immitis; Filaria spp., Filaria oculi; Onchocerca spp., Onchocerca cervicalis, Onchocerca gibsoni, pharyngeal filaments Insect (Onchocerca gutturosa);
(B) Setaria digitata, Setaria equina, Setaria labiatopapillosa, nematodes of the Setariidae family, such as Setaria spp. , Marshalli marshalli; Wuchereria bancrofti of the genus Wuchereria spp.;
(C) Filariidae nematodes, such as Parafilaria spp., Parafilaria multipapillosa; Stephanofilaria spp., Stephanofilaria assam. Ensis (Stephanofilaria assamensis), Stephanofilaria dedoesi, Stephanofilaria kaeli, Okinawa filamentous insect (Stephanofilaria okinawaensis), Stephanofilaria stilesi.

(11) Nematodes of the order Spirurida (a) Gnathostomiasis (Gnathostomatidae) nematodes, for example, Gnathostoma doloresi of the genus Gnathostoma spp. , Gnathostoma spinigerum;
(B) Habronematidae nematodes, such as Habronema spp., Habronema majus, Habronema microstoma, Habronema muscae; Draschia Draschia megastoma of the genus (Draschia spp.);
(C) Physalopteridae nematodes, such as Physaloptera spp., Physaloptera canis, Physaloptera cesticillata, Physaloptera erdociona, Physaloptera erdoc. Physaloptera felidis, Egyptian cat gastrointestinal worm (Physaloptera gemina), Physaloptera papilloradiata, cat gastric worm (Physaloptera praeputialis), Physaloptera pseudopraerutialis rara), Physaloptera sibirica, Physaloptera vulpineus;
(D) Gongylonematidae nematodes, such as the Gongylonema spp., Gongylonema pulchrum;
(E) Nematodes of the family Spirocercidae, such as Ascarops spp., Ascarops strongylina;
(F) Nematodes of the family Thelaziaidae, such as Thelazia spp., Thelazia callipaeda, Thelazia gulosa, Thelazia lacrymalis, Thelazia rhodes. Insects (Thelazia rhodesi), Thelazia skrjabini.

[Control agents for other pests]
The compound of the present invention also has poisonous needles and poisonous liquids, pests that damage human animals, pests that transmit various pathogens and pathogens, and pests that cause discomfort to humans (toxic pests, sanitary pests, and unpleasant pests). Etc.) is excellent in control effect.

A specific example is shown below.
(1) Hymenoptera pests, Vespidaceae (Argidae) bees, Gall wasps (Cynipidae) bees, Vespids (Diprionidae) bees, Ali family (Formicidae) ants, Velvet ants (Mutillidae) bees, A bee of the Vespidae family.

(2) Other pests Cockroaches (Blattodea), termites (termite), spiders (Araneae), mucades (cetipede), millipedes (millipede), crustacea (crustacea), Nanjing insects (Cimex lectularius).

[Pharmaceutical prescription]
Some examples of formulations of the pest control agents, insecticides or acaricides, ectoparasite control agents or endoparasite control or control agents of the present invention are shown, but the additives and addition ratios are in the formulations of these preparation examples. It should not be limited and can be varied over a wide range. The part during formulation indicates the part by weight.

The pharmaceutical formulations for agriculture and horticulture and paddy rice are shown below.
(Formation 1: wettable powder)
40 parts of the compound of the present invention, 53 parts of diatomaceous earth, 4 parts of higher alcohol sulfate ester, and 3 parts of alkylnaphthalene sulfonate are uniformly mixed and finely pulverized to obtain a wettable powder having 40% of the active ingredient.
(Formation 2: Emulsion)
30 parts of the compound of the present invention, 33 parts of xylene, 30 parts of dimethylformamide, and 7 parts of polyoxyethylene alkyl allyl ether are mixed and dissolved to obtain an emulsion containing 30% of the active ingredient.
(Formation 3: Granules)
5 parts of the compound of the present invention, 40 parts of talc, 38 parts of clay, 10 parts of bentonite, and 7 parts of sodium alkyl sulfate are uniformly mixed and finely pulverized, and then granulated into granules having a diameter of 0.5 to 1.0 mm. To obtain granules having 5% of the active ingredient.
(Formation 4: Granules)
5 parts of the compound of the present invention, 73 parts of clay, 20 parts of bentonite, 1 part of sodium dioctyl sulfosuccinate, and 1 part of potassium phosphate were thoroughly pulverized and mixed, water was added and kneaded well, and then granulated and dried. Obtain granules with 5% active ingredient.
(Formula 5: Suspension)
10 parts of the compound of the present invention, 4 parts of polyoxyethylene alkyl allyl ether, 2 parts of polycarboxylic acid sodium salt, 10 parts of glycerin, 0.2 part of xanthan gum, and 73.8 parts of water are mixed to reduce the particle size to 3 microns or less. Wet grind to obtain a suspension of 10% active ingredient.

The formulation of the ectoparasite control agent or the endoparasite control or control agent is shown below.
(Formation 6: Granules)
Five parts of the compound of the present invention are dissolved in an organic solvent to obtain a solution, the solution is sprayed onto 94 parts of kaolin and 1 part of white carbon, and then the solvent is evaporated under reduced pressure. Granules of this type can be mixed with animal food.
(Formation 7: Injectable)
0.1 to 1 part of the compound of the present invention and 99 to 99.9 parts of peanut oil are uniformly mixed, and then sterilized by filtration through a sterilization filter.
(Formation 8: Poaon agent)
A poreon agent is obtained by uniformly mixing 5 parts of the compound of the present invention, 10 parts of myristic acid ester, and 85 parts of isopropanol.
(Formation 9: Spot-on agent)
10 to 15 parts of the compound of the present invention, 10 parts of palmitic acid ester, and 75 to 80 parts of isopropanol are uniformly mixed to obtain a spot-on agent.
(Formula 10: Spray)
A spray agent is obtained by uniformly mixing 1 part of the compound of the present invention, 10 parts of propylene glycol, and 89 parts of isopropanol.

Next, a synthesis example will be shown, and the present invention will be described in more detail. However, the present invention is not limited by the following synthetic examples.

[Example 1]
2- (5-(1- (5- (3,5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazole-3-yl) ethyl) -1H-1,2,4- Triazole-1-yl) pyridine [2- (5-(1- (5- (3,5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazol-3-yl) ethyl) -1H- Synthesis of 1,2,4-triazol-1-yl) pyridine] (Compound No. A-1)

[Step 1]
Synthesis of 3-ethoxy-3-imino-2-methylpropanoate hydrochloride

Ethyl 2-cyanopropionate (10 g) was dissolved in a mixed solvent of toluene (35 mL) and ethanol (7.1 mL) and cooled to 0 ° C. It was bubbled with hydrogen chloride gas for 40 minutes. After the bubbling was completed, the mixture was stirred at room temperature for 1 day.
The solvent was evaporated under reduced pressure, and the obtained solid residue was suspended in a mixed solvent of diethyl ether (30 mL) and cyclohexane (30 mL), and cooled to 0 ° C. Then it was filtered. The obtained filter medium was washed with cyclohexane and then dried to obtain the desired product (14.01 g).

３−エトキシ−３−イミノ−２−メチルプロピオン酸エチル塩酸塩（５９４．０ｍｇ）をジクロロメタン（５．７ｍＬ）に懸濁させ、０℃に冷却した。これにＮ−エチルジイソプロピルアミン（１．０ｍＬ）および３，５−ビス（トリフルオロメチル）ベンゾイルクロリド（０．６２ｍＬ）を加え、室温で７時間撹拌した。
これに水を添加し、次いでジクロロメタンで抽出した。有機層を硫酸マグネシウムで乾燥させた。硫酸マグネシウムをろ過にて除き、濾液から溶媒を減圧留去して、黄色油状物（１．２８ｇ）を得た。
得られた油状物をジクロロメタン（１４．２ｍＬ）に溶解させ、これに室温で１．０Ｍヒドラジン−テトラヒドロフラン溶液（３．２ｍＬ）を添加して、室温で１日間撹拌した。それに水を添加し、次いでジクロロメタンで抽出した。有機層を水で洗浄し、硫酸マグネシウムで乾燥させた。硫酸マグネシウムをろ過にて除き、ろ液から溶媒を減圧留去した。残渣をシリカゲルカラムクロマトグラフィーで精製し、目的物（６０９．４ ｍｇ）を得た。 [Step 2] Ethyl 2- (5- (3,5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazole-3-yl) propionate [ethyl 2- (5- (3, 3,,) Synthesis of 5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazol-3-yl) propanoate]

Ethyl 3-ethoxy-3-imino-2-methylpropionate (594.0 mg) was suspended in dichloromethane (5.7 mL) and cooled to 0 ° C. To this was added N-ethyldiisopropylamine (1.0 mL) and 3,5-bis (trifluoromethyl) benzoyl chloride (0.62 mL), and the mixture was stirred at room temperature for 7 hours.
Water was added to this and then extracted with dichloromethane. The organic layer was dried over magnesium sulfate. Magnesium sulfate was removed by filtration, and the solvent was distilled off under reduced pressure from the filtrate to obtain a yellow oil (1.28 g).
The obtained oil was dissolved in dichloromethane (14.2 mL), a 1.0 M hydrazine-tetrahydrofuran solution (3.2 mL) was added thereto at room temperature, and the mixture was stirred at room temperature for 1 day. Water was added to it and then extracted with dichloromethane. The organic layer was washed with water and dried over magnesium sulfate. Magnesium sulfate was removed by filtration, and the solvent was distilled off under reduced pressure from the filtrate. The residue was purified by silica gel column chromatography to obtain the desired product (609.4 mg).

[Step 3] 2- (5- (3,5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazole-3-yl) propionic acid amide [2- (5- (3,5) -Bis (trifluoromethyl) phenyl) -4H-1,2,4-triazol-3-yl) propanamide] synthesis

2- (5- (3,5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazole-3-yl) ethyl propionate (791.9 mg) dissolved in tetrahydrofuran (4.2 mL) Then, 2N aqueous sodium hydroxide solution (4.2 mL) was added thereto, and the mixture was stirred at 40 ° C. for 1 day. This was allowed to cool to room temperature. The pH was adjusted to about 3 by adding 2N hydrochloric acid to this. This was extracted 3 times with ethyl acetate, the organic layer was washed with water and then dried over magnesium sulfate. Magnesium sulfate was removed by filtration, and the solvent was distilled off from the filtrate under reduced pressure to obtain a solid residue (703.0 mg). The obtained solid residue was dissolved in dichloromethane (5.9 mL), oxalyl chloride (0.25 mL) and 2 drops of DMF were added thereto, and the mixture was stirred at room temperature for 2 hours. Then the solvent was distilled off. The obtained residue was dissolved in tetrahydrofuran (3.9 mL), and this was added dropwise to concentrated ammonia water (3.9 mL) cooled to 0 ° C. This was stirred at room temperature for 1 hour. Then, the solution was separated with ethyl acetate and water, the organic layer was washed with water, and then dried with magnesium sulfate. Magnesium sulfate was removed by filtration, and the solvent was distilled off under reduced pressure from the filtrate. The residue was purified by silica gel column chromatography to obtain the desired product (423.0 mg).

[Step 4] 2- (5-(1- (5- (3,5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazole-3-yl) ethyl) -1H-1, 2,4-Triazole-1-yl) pyridine [2- (5- (5- (1- (5- (3,5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazol-3-yl) ethyl ) -1H-1,2,4-triazol-1-yl) pyridine]

2- (5- (3,5-bis (trifluoromethyl) phenyl) -4H-1,2,4-triazole-3-yl) propionic acid amide (310.0 mg) in dichloromethane (1.6 mL) It was dissolved, DMF-dimethylacetal (0.18 mL) was added thereto, and the mixture was heated under reflux for 35 minutes. The solvent was distilled off under reduced pressure. The residue was dissolved in dioxane (0.8 mL) and acetic acid (0.8 mL), 2-hydrazinopyridine (115.0 mg) was added, and the mixture was stirred at 40 ° C. for 2 hours. Saturated aqueous sodium hydrogen carbonate was added thereto to stop the reaction. Then, the solution was separated with ethyl acetate and water, the organic layer was washed with water, and then dried with magnesium sulfate. Magnesium sulfate was removed by filtration, and the solvent was distilled off under reduced pressure from the filtrate. The residue was purified by silica gel column chromatography to obtain the desired product (58 mg).

Table 1 shows an example of the compound of the present invention produced by the same method as in the above-mentioned Examples. The physical property data of the compound was entered in the "Physical characteristics" column. As the physical property data, the melting point (mp) is described.

[Biological test]
The following test examples show that the compound of the present invention is useful as an active ingredient of a pest control agent. "Part" is based on weight.

(Preparation of test emulsion)
An emulsion (I) containing 5% of the active ingredient was prepared by mixing and dissolving 5 parts by weight of the compound of the present invention, 93.6 parts by weight of dimethylformamide, and 1.4 parts by weight of polyoxyethylene alkylaryl ether.
(Preparation of control emulsion)
Emulsion (II) was prepared by mixing and dissolving 93.6 parts by weight of dimethylformamide and 1.4 parts by weight of polyoxyethylene alkylaryl ether.

(1) Emulsion test for armyworm (I) was diluted with water so that the concentration of the compound of the present invention was 125 ppm. The corn leaf pieces were immersed in the diluted solution for 30 seconds. The corn leaf pieces were placed in a petri dish and 5 second-instar larvae of Mythimna separata were released.
The petri dish was left in a thermostatic chamber at a temperature of 25 ° C. and a humidity of 60% during the test period. When 6 days had passed since the insect was released, the life or death was judged and the insecticidal rate was calculated. The test was performed in two iterations.
The efficacy test of the compound of Compound No. A-1 against Mythimna separata was carried out. This compound showed an insecticidal rate of 80% or more with respect to armyworm.

(2) Emulsion Test for Spodoptera litura Emulsion (I) was diluted with water so that the concentration of the compound of the present invention was 125 ppm. The cabbage leaves were immersed in the diluted solution for 30 seconds. The cabbage leaves were placed in a petri dish and 5 second-instar larvae of Spodoptera litura were released. The petri dish was left in a thermostatic chamber at a temperature of 25 ° C. and a humidity of 60% during the test period. When 6 days had passed since the insect was released, the life or death was judged and the insecticidal rate was calculated. The test was performed in two iterations.
The compounds of Compound Nos. A-1, A-2, A-3, and A-4 were tested for efficacy against Spodoptera litura. Both compounds showed an insecticidal rate of 80% or more with respect to Spodoptera litura.

Randomly selected compounds of the present invention exert the above-mentioned effects. Therefore, the compounds of the present invention include compounds that could not be shown in the examples, and pest control, acaricide, especially insecticide, etc. It can be understood that it is a compound having the effect of.

Claims (7)

A compound represented by the formula (I) or a salt thereof.

(In formula (I),
X is a halogeno group, a substituted or unsubstituted C1-6 alkyl group, a hydroxyl group, a substituted or unsubstituted C1-6 alkoxy group, a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkyl. Sulfinyl group, substituted or unsubstituted C1-6 alkylsulfonyl group, substituted or unsubstituted C3-6 cycloalkyl group, substituted or unsubstituted C3-6 cycloalkyloxy group, substituted or unsubstituted C3-6 cycloalkylthio Group, substituted or unsubstituted C3-6 cycloalkylsulfinyl group, substituted or unsubstituted C3-6 cycloalkylsulfonyl group, nitro group, or cyano group.
n indicates the number of X and is an integer of 1 to 5.
Q ¹ represents a substituted or unsubstituted 5-membered heterocyclylene group.
A represents a substituted or unsubstituted C1-2 alkylene group.
Y ¹ represents a nitrogen atom or ^a group represented by CR a,
Y ² represents a group represented by ^a nitrogen atom or CR a,
R ^a each independently represent a hydrogen atom, a halogeno group or a substituted or unsubstituted C1~6 alkyl,
Q ² represents a substituted or unsubstituted 6-membered heteroaryl group. ) The compound according to claim 1 or a salt thereof, wherein Q ^{1 is a substituted or unsubstituted triazolylen group.} The compound according to claim 1 or 2, or a salt thereof, wherein Q ^{2 is a substituted or unsubstituted pyridyl group or a substituted or unsubstituted pyrimidinyl group.} A pest control agent containing at least one selected from the group consisting of the compound according to any one of claims 1 to 3 and a salt thereof as an active ingredient. An insecticide or acaricide containing at least one selected from the group consisting of the compound according to any one of claims 1 to 3 and a salt thereof as an active ingredient. An ectoparasite control agent containing at least one selected from the group consisting of the compound according to any one of claims 1 to 3 and a salt thereof as an active ingredient. An endoparasite control or extermination agent containing at least one selected from the group consisting of the compound according to any one of claims 1 to 3 and a salt thereof as an active ingredient.