JP5550913B2 - Tetrazoyloxime derivative and salt thereof, and plant disease control agent - Google Patents

Description

  The present invention relates to a novel tetrazoyloxime derivative and a salt thereof, and a plant disease control agent containing at least one selected from them as an active ingredient.

In the cultivation of agricultural and horticultural crops, many control agents have been proposed for crop diseases. For example, Patent Documents 1 to 6 disclose tetrazoyloxime derivatives having a structure similar to that of the compound of the present invention, and have been proposed for use as plant disease control agents.
However, conventional plant disease control agents have insufficient control efficacy, are restricted in their use due to the emergence of drug-resistant pathogens, cause phytotoxicity and contamination of plants, or livestock fish In many cases, it is not always a satisfactory control drug. Accordingly, there is a demand for the development of a new plant disease control agent that can be safely used with few such drawbacks.

JP 2004-131416 A JP 2004-131392 A JP 2003-137875 A WO2008 / 006873 WO2008 / 006874 WO2008 / 006875

  The present invention has been made in view of the state of the prior art, and contains a novel tetrazoyl oxime derivative and a salt thereof, which are excellent in controlling effects on plant diseases, and at least one selected from them as an active ingredient. An object of the present invention is to provide a plant disease control agent.

  In order to solve the above-mentioned problems, the present inventors have synthesized a number of tetrazoyloxime derivatives and salts thereof and have intensively studied their physiological activities. As a result, the present inventors have found that a tetrazoyloxime derivative represented by the following formula (1) and a salt thereof exhibit excellent control effects against plant diseases and are free from fear of phytotoxicity against useful plants. It came to complete.

  That is, the first of the present invention is a tetrazoyloxime derivative represented by the formula (1) and a salt thereof.

式（１）中、Ｘは、ハロゲン原子、Ｃ_1-8アルキル基、Ｃ_1-8アルコキシ基、シアノ基、Ｃ_1-8アルキルスルホニル基、ニトロ基、Ｃ_1-8ハロアルキル基、または無置換の若しくは置換基を有するアリール基を表す。ｎ１はＸの数を表し、０〜５のいずれかの整数である。ｎ１が２以上のとき、Ｘ同士は互いに同一であっても、相異なっていてもよい。
Ａは、式（２）または式（３）で表されるテトラゾイル基を表す。

In formula (1), X is a halogen atom, a C _1-8 alkyl group, a C _1-8 alkoxy group, a cyano group, a C _1-8 alkylsulfonyl group, a nitro group, a C _1-8 haloalkyl group, or unsubstituted. Or an aryl group having a substituent. n1 represents the number of X and is an integer of 0-5. When n1 is 2 or more, Xs may be the same as or different from each other.
A represents a tetrazoyl group represented by formula (2) or formula (3).

式（２）中、ＹはＣ_1-8アルキル基を表す。

In formula (2), Y represents a C _1-8 alkyl group.

式（３）中、Ｙは前記と同じ意味を表す。
Ｈｅｔは、式（４）で表されるピリジル基、または式（５）で表されるチアゾイル基を表す。

In formula (3), Y represents the same meaning as described above.
Het represents a pyridyl group represented by the formula (4) or a thiazoyl group represented by the formula (5).

式（４）中、Ｒは、ハロゲン原子、シアノ基、ニトロ基、水酸基、チオール基、ホルミル基、カルボキシル基、無置換の若しくは置換基を有するアミノ基、無置換の若しくは置換基を有するＣ_1-8アルキル基、無置換の若しくは置換基を有するＣ_2-8アルケニル基、無置換の若しくは置換基を有するＣ_2-8アルキニル基、無置換の若しくは置換基を有するアリール基、無置換の若しくは置換基を有するヘテロ環基、ＯＲ¹、Ｓ（Ｏ）_mＲ¹、ＣＯＲ¹、またはＣＯ₂Ｒ¹を表す。Ｒ¹は、無置換の若しくは置換基を有するアミノ基、無置換の若しくは置換基を有するＣ_1-8アルキル基、無置換の若しくは置換基を有するＣ_3-8シクロアルキル基、無置換の若しくは置換基を有するＣ_2-8アルケニル基、無置換の若しくは置換基を有するＣ_2-8アルキニル基、無置換の若しくは置換基を有するアリール基、または無置換の若しくは置換基を有するヘテロ環基を表す。ｍは括弧内の酸素原子の数を表し、０〜２のいずれかの整数である。
ｎ２はＲの数を表し、０〜３のいずれかの整数である。ｎ２が２以上のとき、複数のＲ同士は、互いに同一であっても、相異なっていてもよい。
Ｚは、式（ａ）若しくは式（ｂ）で表される基を表す。

In the formula (4), R represents a halogen atom, a cyano group, a nitro group, a hydroxyl group, a thiol group, a formyl group, a carboxyl group, an unsubstituted or substituted amino group, an unsubstituted or substituted C _{1. -8} alkyl group, unsubstituted or substituted C _2-8 alkenyl group, unsubstituted or substituted C _2-8 alkynyl group, unsubstituted or substituted aryl group, unsubstituted or It represents a heterocyclic group having a substituent, OR ¹ , S (O) _m R ¹ , COR ¹ , or CO ₂ R ¹ . R ¹ is an unsubstituted or substituted amino group, an unsubstituted or substituted C _1-8 alkyl group, an unsubstituted or substituted C _3-8 cycloalkyl group, unsubstituted or A C _2-8 alkenyl group having a substituent, an unsubstituted or substituted C _2-8 alkynyl group, an unsubstituted or substituted aryl group, or an unsubstituted or substituted heterocyclic group; Represent. m represents the number of oxygen atoms in parentheses and is an integer of 0-2.
n2 represents the number of R and is an integer of 0-3. When n2 is 2 or more, the plurality of Rs may be the same as or different from each other.
Z represents a group represented by the formula (a) or the formula (b).

式（ａ）中、Ｑ¹は、無置換の若しくは置換基を有するアルキル基、無置換の若しくは置換基を有するアラルキル基、無置換の若しくは置換基を有するアルコキシ基、無置換の若しくは置換基を有するアラルキルオキシ基、無置換の若しくは置換基を有するアルキルチオ基、無置換の若しくは置換基を有するアラルキルチオ基、またはＮＲ²⁰Ｒ²¹を表す。Ｒ²⁰およびＲ²¹は、それぞれ独立に、水素原子、無置換の若しくは置換基を有するアルキル基、無置換の若しくは置換基を有するアラルキル基、または無置換の若しくは置換基を有するアリール基を表す。

In formula (a), Q ¹ represents an unsubstituted or substituted alkyl group, an unsubstituted or substituted aralkyl group, an unsubstituted or substituted alkoxy group, an unsubstituted or substituted group. An aralkyloxy group having an unsubstituted or substituted alkylthio group, an unsubstituted or substituted aralkylthio group, or NR ²⁰ R ²¹ . R ²⁰ and R ²¹ each independently represents a hydrogen atom, an unsubstituted or substituted alkyl group, an unsubstituted or substituted aralkyl group, or an unsubstituted or substituted aryl group.

式（ｂ）中、Ｑ²は、無置換の若しくは置換基を有するアルキルチオ基、無置換の若しくは置換基を有するアラルキルチオ基、またはＮＲ³⁰Ｒ³¹を表す。Ｒ³⁰およびＲ³¹は、それぞれ独立に、水素原子、無置換の若しくは置換基を有するアルキル基、無置換の若しくは置換基を有するアラルキル基、無置換の若しくは置換基を有するアルコキシ基、無置換の若しくは置換基を有するアリール基、スルホニル基、無置換の若しくは置換基を有するアミノ基、またはＣＯＲ¹を表し、Ｒ³⁰およびＲ³¹は一緒になって環を形成してもよい。Ｒ¹は前記と同じ意味を表す。

In formula (b), Q ² represents an unsubstituted or substituted alkylthio group, an unsubstituted or substituted aralkylthio group, or NR ³⁰ R ³¹ . R ³⁰ and R ³¹ are each independently a hydrogen atom, an unsubstituted or substituted alkyl group, an unsubstituted or substituted aralkyl group, an unsubstituted or substituted alkoxy group, an unsubstituted group Alternatively, it represents an aryl group having a substituent, a sulfonyl group, an unsubstituted or substituted amino group, or COR ¹ , and R ³⁰ and R ³¹ may form a ring together. R ¹ represents the same meaning as described above.

式（５）中、Ｒ¹¹は、水素原子、ハロゲン原子、シアノ基、ニトロ基、水酸基、チオール基、ホルミル基、カルボキシル基、無置換の若しくは置換基を有するアミノ基、無置換の若しくは置換基を有するＣ_1-8アルキル基、無置換の若しくは置換基を有するＣ_2-8アルケニル基、無置換の若しくは置換基を有するＣ_2-8アルキニル基、無置換の若しくは置換基を有するアリール基、無置換の若しくは置換基を有するヘテロ環基、ＯＲ¹、Ｓ（Ｏ）_mＲ¹、ＣＯＲ¹、またはＣＯ₂Ｒ¹を表す。Ｒ¹およびｍは、前記と同じ意味を表す。
Ｚは、前記と同じ意味を表す。

In formula (5), R ¹¹ is a hydrogen atom, a halogen atom, a cyano group, a nitro group, a hydroxyl group, a thiol group, a formyl group, a carboxyl group, an unsubstituted or substituted amino group, an unsubstituted or substituted group A C _1-8 alkyl group having an unsubstituted or substituted C _2-8 alkenyl group, an unsubstituted or substituted C _2-8 alkynyl group, an unsubstituted or substituted aryl group, It represents an unsubstituted or substituted heterocyclic group, OR ¹ , S (O) _m R ¹ , COR ¹ , or CO ₂ R ¹ . R ¹ and m represent the same meaning as described above.
Z represents the same meaning as described above.

In the present invention, preferred tetrazoyloxime derivatives and salts thereof are those in which n1 is 0 and / or Y is a methyl group. In the present invention, a suitable tetrazoyloxime derivative and a salt thereof include an aralkyl group in which Q ¹ in the formula (a) is an aralkyloxy group, an alkoxy group having ₃ or more C3, an aralkylthio group, an alkylthio group, an oxy group, ₄ or more alkyl groups or NR ²⁰ R ²¹ , or Q ² in the formula (b) is an aralkylthio group, an alkylthio group, or NR ³⁰ R ³¹ .

A second aspect of the present invention is a plant disease control agent containing as an active ingredient at least one selected from the above tetrazoyloxime derivatives or salts thereof.
In the present specification, the “C _ab OO group” and the “C _c or more XXX group” are those in which the number of carbon elements constituting the group is a to b and c or more. It is shown that.

  The tetrazoyl oxime derivative and its salt of the present invention show an excellent control effect against plant diseases, and there is no fear of phytotoxicity against useful plants. Since the plant disease control agent of the present invention contains at least one selected from the tetrazoyl oxime derivative of the present invention or a salt thereof, the disease control in the cultivation of agricultural crops is effective, while There is no phytotoxicity or pollution to the environment, and the toxicity to human and livestock fish is low.

  Hereinafter, the present invention will be described in detail by dividing it into 1) tetrazoyloxime derivatives and salts thereof, and 2) plant disease control agents.

1) Tetrazoyl oxime derivative and salt thereof The tetrazoyl oxime derivative of the present invention is a compound represented by the formula (1).

In the formula (1), X is a halogen atom, a C _1-8 alkyl group, a C _1-8 alkoxy group, a cyano group, a C _1-8 alkylsulfonyl group, a nitro group, a C _1-8 haloalkyl group, or nothing. Represents a substituted or substituted aryl group;

Specific examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
Specific examples of the C _1-8 alkyl group include methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, i-butyl group, s-butyl group, t-butyl group, n- A pentyl group, n-hexyl group, etc. are mentioned.
Specific examples of the C _1-8 alkoxy group include methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, i-butoxy group, s-butoxy group, t-butoxy group, n- A hexyloxy group etc. are mentioned.
Specific examples of the C _1-8 alkylsulfonyl group include a methylsulfonyl group, an ethylsulfonyl group, an n-propylsulfonyl group, an i-propylsulfonyl group, and a t-butylsulfonyl group.
Specific examples of the C _1-8 haloalkyl group include a fluoromethyl group, a chloromethyl group, a bromomethyl group, a difluoromethyl group, a dichloromethyl group, a trifluoromethyl group, a trichloromethyl group, a trifluoroethyl group, a pentafluoroethyl group, 3,3,3,2,2-pentafluoropropyl group, 2,2,2-trifluoro-1-trifluoromethylethyl group and the like can be mentioned.

An aryl group means a monocyclic or polycyclic aryl group. In the polycyclic aryl group, as long as at least one ring is an aromatic ring, the remaining ring may be a saturated alicyclic ring, an unsaturated alicyclic ring, or an aromatic ring. Of the aryl groups, a C _6-10 aryl group is preferred. Specific examples of the unsubstituted aryl group include a phenyl group, a 1-naphthyl group, a 2-naphthyl group, an azulenyl group, an indanyl group, and a tetralinyl group.

The “substituent” in the aryl group having a substituent is not particularly limited as long as it is chemically acceptable. Specific examples include the substituents exemplified below.
(1) Halogen atoms such as fluorine atom, chlorine atom, bromine atom, iodine atom; (2) methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, s-butyl group, i- Alkyl groups such as butyl, s-butyl, t-butyl, n-pentyl and n-hexyl; (3) cycloalkyl such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl (4) alkoxy group such as methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, i-butoxy group, s-butoxy group, t-butoxy group, etc .; (5) vinyl group 1-propenyl group, 2-propenyl group, 1-butenyl group, 2-butenyl group, 3-butenyl group, 1-methyl-2-propenyl group, 2-methyl-2-propenyl group, 1-pentenyl group, 2 - Nthenyl group, 3-pentenyl group, 4-pentenyl group, 1-methyl-2-butenyl group, 2-methyl-2-butenyl group, 1-hexenyl group, 2-hexenyl group, 3-hexenyl group, 4-hexenyl group Alkenyl groups such as 5-hexenyl group; (6) cycloalkenyl groups such as 2-cyclopropenyl group, 2-cyclopentenyl group, 3-cyclohexenyl group, 4-cyclooctenyl group; (7) vinyloxy group, allyloxy group, Alkenyloxy groups such as 1-propenyloxy group and 2-butenyloxy group; (8) ethynyl group, 1-propynyl group, 2-propynyl group, 1-butynyl group, 2-butynyl group, 3-butynyl group, 1-methyl 2-propynyl group, 2-methyl-3-butynyl group, 1-pentynyl group, 2-pentynyl group, 3-pentynyl group, 4-pentynyl group, 1- Alkynyl groups such as til-2-butynyl group, 2-methyl-3-pentynyl group, 1-hexynyl group and 1,1-dimethyl-2-butynyl group; (9) Alkynyloxy such as ethynyloxy group and propargyloxy group Group; (10) aryl group such as phenyl group, 1-naphthyl group, 2-naphthyl group;

  (11) aryloxy groups such as phenoxy group and 1-naphthoxy group; (12) aralkyl groups such as benzyl group and phenethyl group; (13) aralkyloxy groups such as benzyloxy group and phenethyloxy group; (14) formyl group Acetyl group such as acetyl group, propionyl group, benzoyl group, cyclohexylcarbonyl group, phthaloyl group; (15) methoxycarbonyl group, ethoxycarbonyl group, n-propoxycarbonyl group, i-propoxycarbonyl group, n-butoxycarbonyl group, alkoxycarbonyl groups such as t-butoxycarbonyl group; (16) carboxyl group; (17) hydroxyl group; (18) chloromethyl group, chloroethyl group, 1,2-dichloro-n-propyl group, 1-fluoro-n-butyl Groups, haloalkyl groups such as perfluoro-n-pentyl group; (19) 2-chloro-n-propoxy Haloalkoxy groups such as a group, 2,3-dichlorobutoxy group and trifluoromethoxy group; (20) haloalkenyl groups such as 2-chloro-1-propenyl group and 2-fluoro-1-butenyl group; , Haloalkynyl groups such as 4-dichloro-1-butynyl group, 4-fluoro-1-pentynyl group, 5-bromo-2-pentynyl group;

  (22) haloalkenyloxy groups such as 2-chloro-1-propenyloxy group and 3-bromo-2-butenyloxy group; (23) haloalkynyl groups such as 3-chloro-propargyl group and 3-iodo-propargyl group; (24) haloalkynyloxy groups such as 3-chloro-propargyloxy group and 3-iodo-propargyloxy group; (25) haloaryl groups such as 4-chlorophenyl group, 4-fluorophenyl group and 2,4-dichlorophenyl group; (26) Haloaryloxy groups such as 4-fluorophenoxy group and 4-chloro-1-naphthoxy group; (27) Halogen-substituted acyls such as chloroacetyl group, trifluoroacetyl group, trichloroacetyl group and 4-chlorobenzoyl group (28) Alkoxy such as methoxymethyl group, ethoxymethyl group, 1-ethoxyethyl group, 2-ethoxyethyl group, etc. (29) alkoxyalkoxy groups such as methoxymethoxy group, ethoxymethoxy group, 1-ethoxyethoxy group, 2-ethoxyethoxy group; (30) cyano group;

(31) Isocyano group; (32) Nitro group; (33) Isocyanato group; (34) Cyanato group; (35) Amino group (NH ₂ group); (36) Methylamino group, dimethylamino group, diethylamino group, etc. (37) arylamino groups such as anilino group, naphthylamino group and anthranylamino group; (38) aralkylamino groups such as benzylamino group and phenethylamino group; (39) methylsulfonylamino group and ethylsulfonylamino group; Alkylsulfonylamino groups such as a group, n-propylsulfonylamino group, i-propylsulfonylamino group, n-butylsulfonylamino group; (40) arylsulfonylamino groups such as phenylsulfonylamino group; (41) piperazinylsulfonyl A heteroarylsulfonylamino group such as an amino group;

  (42) acylamino groups such as formylamino group, acetylamino group, propanoylamino group, butyrylamino group, i-propylcarbonylamino group, benzoylamino group; (43) alkoxycarbonyl such as methoxycarbonylamino group, ethoxycarbonylamino group, etc. (44) fluoromethylsulfonylamino group, chloromethylsulfonylamino group, bromomethylsulfonylamino group, difluoromethylsulfonylamino group, dichloromethylsulfonylamino group, 1,1-difluoroethylsulfonylamino group, trifluoromethylsulfonyl Haloalkylsulfonylamino groups such as amino group, 2,2,2-trifluoroethylsulfonylamino group, pentafluoroethylsulfonylamino group; (45) bis (methylsulfonyl) amino group, bis (eth Rusulfonyl) amino group, (ethylsulfonyl) (methylsulfonyl) amino group, bis (n-propylsulfonyl) amino group, bis (i-propylsulfonyl) amino group, bis (n-butylsulfonyl) amino group, bis (t -Bis (alkylsulfonyl) amino groups such as butylsulfonyl) amino group;

  (46) Bis (fluoromethylsulfonyl) amino group, bis (chloromethylsulfonyl) amino group, bis (bromomethylsulfonyl) amino group, bis (dichloromethylsulfonyl) amino group, bis (1,1-difluoroethylsulfonyl) amino A bis (haloalkylsulfonyl) amino group such as a group, bis (trifluoromethylsulfonyl) amino group, bis (2,2,2-trifluoroethylsulfonyl) amino group, bis (pentafluoroethylsulfonyl) amino group; An unsubstituted or substituted hydrazino group such as a hydrazino group, an N′-phenylhydrazino group, an N′-methoxycarbonylhydrazino group, an N′-acetylhydrazino group, an N′-methylhydrazino group; ) Aminocarbonyl group, dimethylaminocarbonyl group, phenylaminocarb An unsubstituted or substituted aminocarbonyl group such as a bonyl group or an N-phenyl-N-methylaminocarbonyl group; (49) hydrazinocarbonyl group, N′-methylhydrazinocarbonyl group, N′-phenylhydrazino An unsubstituted or substituted hydrazinocarbonyl group such as a carbonyl group; (50) N-methyliminomethyl group, 1-N-phenyliminoethyl group, N-hydroxyiminomethyl group, N-methoxyiminomethyl group, etc. An unsubstituted or substituted iminoalkyl group;

  (51) thiol group; (52) isothiocyanato group; (53) thiocyanato group; (54) methylthio group, ethylthio group, n-propylthio group, i-propylthio group, n-butylthio group, i-butylthio group, s-butylthio group Groups, alkylthio groups such as t-butylthio groups; (55) alkenylthio groups such as vinylthio groups and allylthio groups; (56) alkynylthio groups such as ethynylthio groups and propargylthio groups; (57) phenylthio groups and naphthylthio groups; (58) heteroarylthio groups such as 2-piperidylthio group and 3-pyridazylthio group; (59) aralkylthio groups such as benzylthio group and phenethylthio group; (60) 2-pyridylmethylthio group and 2-furyl. Heteroarylalkylthio groups such as methylthio group; (61) methylthiocarbonyl group, ethylthiocarbonyl group, n-propyl Alkylthiocarbonyl groups such as a thiocarbonyl group, i-propylthiocarbonyl group, n-butylthiocarbonyl group, i-butylthiocarbonyl group, s-butylthiocarbonyl group, t-butylthiocarbonyl group;

  (62) alkylthioalkyl groups such as methylthiomethyl group and 1-methylthioethyl group; (63) arylthioalkyl groups such as phenylthiomethyl group and 1-phenylthioethyl group; (64) methylthiomethoxy group and 1-methylthioethoxy group. Alkylthioalkoxy groups such as groups; (65) arylthioalkoxy groups such as phenylthiomethoxy groups and 1-phenylthioethoxy groups; (66) alkylsulfinyl groups such as methylsulfinyl groups, ethylsulfinyl groups and t-butylsulfinyl groups; (67) Alkenylsulfinyl groups such as allylsulfinyl groups; (68) Alkynylsulfinyl groups such as propargylsulfinyl groups; (69) Arylsulfinyl groups such as phenylsulfinyl groups; (70) 2-pyridylsulfinyl groups, 3-pyridylsulfinyl groups Heteroaryl sulfi (71) Aralkylsulfinyl groups such as benzylsulfinyl group and phenethylsulfinyl group; (72) Heteroarylalkylsulfinyl groups such as 2-pyridylmethylsulfinyl group and 3-pyridylmethylsulfinyl group;

  (73) alkylsulfonyl groups such as methylsulfonyl group, ethylsulfonyl group, t-butylsulfonyl group; (74) alkenylsulfonyl groups such as allylsulfonyl group; (75) alkynylsulfonyl groups such as propargylsulfonyl group; (76) phenyl Arylsulfonyl groups such as sulfonyl groups; (77) heteroarylsulfonyl groups such as 2-pyridylsulfonyl groups and 3-pyridylsulfonyl groups; (78) aralkylsulfonyl groups such as benzylsulfonyl groups and phenethylsulfonyl groups; Heteroarylalkylsulfonyl groups such as pyridylmethylsulfonyl group and 3-pyridylmethylsulfonyl group; (80) furan-2-yl group, furan-3-yl group, thiophen-2-yl group, thiophen-3-yl group, Pyrrol-2-yl group, pyrrol-3-yl group, oxazole-2 -Yl group, oxazol-4-yl group, oxazol-5-yl group, thiazol-2-yl group, thiazol-4-yl group, thiazol-5-yl group, isoxazol-3-yl group, isoxazole- 4-yl group, isoxazol-5-yl group, isothiazol-3-yl group, isothiazol-4-yl group, isothiazol-5-yl group, imidazol-2-yl group, imidazol-4-yl group Imidazol-5-yl group, pyrazol-3-yl group, pyrazol-4-yl group, pyrazol-5-yl group, 1,3,4-oxadiazol-2-yl group, 1,3,4- Unsaturated complex such as thiadiazol-2-yl group, 1,2,3-triazol-4-yl group, 1,2,4-triazol-3-yl group, 1,2,4-triazol-5-yl group Membered cyclic group;

(81) Pyridin-2-yl group, pyridin-3-yl group, pyridin-4-yl group, 5-chloro-3-pyridyl group, 3-trifluoromethyl-2-pyridyl group, pyridazin-3-yl group , Pyridazin-4-yl group, pyrazin-2-yl group, pyrimidin-5-yl group, 1,3,5-triazin-2-yl group, 1,2,4-triazin-3-yl group, etc. (82) tetrahydrofuran-2-yl group, tetrahydropyran-4-yl group, piperidin-3-yl group, pyrrolidin-2-yl group, morpholino group, piperidino group, N-methylpiperazino group, Saturated or partially unsaturated heterocyclic group such as oxazolin-2-yl group; (83) heterocyclic oxy group such as 2-pyridyloxy group and 3-isoxazolyloxy group; (84) 2-pyridylmethyl group; 3-pyridylmethi (85) A heteroarylalkoxy group such as 2-pyridylmethoxy group and 3-pyridylmethoxy group.
These substituents exemplified in (1) to (85) can further have substituents exemplified in (1) to (85) in a chemically acceptable range.

Specific examples of the aryl group having a substituent include 4-fluorophenyl group, 4-chlorophenyl group, 2,4-dichlorophenyl group, 3,4-dichlorophenyl group, 3,5-dichlorophenyl group, 2,6-difluorophenyl. Group, 4-trifluoromethylphenyl group, 4-methoxyphenyl group, 3,4-dimethoxyphenyl group, 3,4-methylenedioxyphenyl group, 4-trifluoromethoxyphenyl group, 4-methoxy-1-naphthyl group Etc.
Among these, X is preferably a halogen atom.

  n1 is any integer of 0 to 5, preferably any integer of 0 to 3, more preferably 0. When n1 is 2 or more, Xs may be the same or different from each other.

A represents a tetrazoyl group represented by formula (2) or formula (3). Of these, a tetrazoyl group represented by the formula (2) is preferable.
In formulas (2) and (3), Y represents a C _1-8 alkyl group. _{Examples of the} C _1-8 alkyl group include the same groups as those enumerated above for X.
Among these, as Y, a C _1-3 alkyl group is preferable, and a methyl group is particularly preferable.

Het represents a pyridyl group represented by the formula (4) or a thiazolyl group represented by the formula (5). Of these, the pyridyl group represented by the formula (4) is preferable.
In the formula (4), R represents a halogen atom, a cyano group, a nitro group, a hydroxyl group, a thiol group, a formyl group, a carboxyl group, an unsubstituted or substituted amino group, an unsubstituted or substituted C _{1. -8} alkyl group, unsubstituted or substituted C _2-8 alkenyl group, unsubstituted or substituted C _2-8 alkynyl group, unsubstituted or substituted aryl group, unsubstituted or It represents a heterocyclic group having a substituent, OR ¹ , S (O) _m R ¹ , COR ¹ , or CO ₂ R ¹ .

Examples of the halogen atom, unsubstituted C _1-8 alkyl group, and unsubstituted or substituted aryl group as R are the same as those described for X.
Specific examples of the unsubstituted C _2-8 alkenyl group as R include a vinyl group, a 1-propenyl group, a 2-propenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, and 1-methyl. 2-propenyl group, 2-methyl-2-propenyl group, 1-pentenyl group, 2-pentenyl group, 3-pentenyl group, 4-pentenyl group, 1-methyl-2-butenyl group, 2-methyl-2- Examples include butenyl group, 1-hexenyl group, 2-hexenyl group, 3-hexenyl group, 4-hexenyl group, 5-hexenyl group and the like.

Specific examples of the unsubstituted C _2-8 alkynyl group as R include ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl. 2-propynyl group, 2-methyl-3-butynyl group, 1-pentynyl group, 2-pentynyl group, 3-pentynyl group, 4-pentynyl group, 1-methyl-2-butynyl group, 2-methyl-3- A pentynyl group, 1-hexynyl group, 1,1-dimethyl-2-butynyl group and the like can be mentioned.

  Specific examples of the unsubstituted heterocyclic group as R include furan-2-yl group, furan-3-yl group, thiophen-2-yl group, thiophen-3-yl group, and pyrrol-2-yl group. Pyrrol-3-yl group, oxazol-2-yl group, oxazol-4-yl group, oxazol-5-yl group, thiazol-2-yl group, thiazol-4-yl group, thiazol-5-yl group, Isoxazol-3-yl group, isoxazol-4-yl group, isoxazol-5-yl group, isothiazol-3-yl group, isothiazol-4-yl group, isothiazol-5-yl group, imidazole- 2-yl group, imidazol-4-yl group, imidazol-5-yl group, pyrazol-3-yl group, pyrazol-4-yl group, pyrazol-5-yl group, 1,3,4- Oxadiazol-2-yl group, 1,3,4-thiadiazol-2-yl group, 1,2,3-triazol-4-yl group, 1,2,4-triazol-3-yl group, 1,2, Unsaturated 5-membered cyclic group such as 4-triazol-5-yl group; pyridin-2-yl group, pyridin-3-yl group, pyridin-4-yl group, 5-chloro-3-pyridyl group, 3- Trifluoromethyl-2-pyridyl group, pyridazin-3-yl group, pyridazin-4-yl group, pyrazin-2-yl group, pyrimidin-5-yl group, 1,3,5-triazin-2-yl group, Unsaturated hetero 6-membered ring groups such as 1,2,4-triazin-3-yl group; tetrahydrofuran-2-yl group, tetrahydropyran-4-yl group, piperidin-3-yl group, pyrrolidin-2-yl group , Morpholino group, piperidino , Piperazino group, N- methylpiperazino group, aziridino group, azetidino group, pyrrolidino group, etc. saturated or partially unsaturated heterocyclic group such as oxazolin-2-yl group.

As R, an amino group having a substituent, a C _1-8 alkyl group having a substituent, a C _2-8 alkenyl group having a substituent, a C _2-8 alkynyl group having a substituent, and a hetero having a substituent Examples of the “substituent” in the cyclic group include the same ones as those shown as the “substituent” in the aryl group having a substituent in X within a chemically acceptable range.
Specific examples of the amino group having a substituent include methylamino group, dimethylamino group, methylethylamino group, diethylamino group, t-butoxycarbonylmethylamino group, t-butoxycarbonylamino group, acetylmethylamino group, and acetylethyl. An amino group, a benzoylmethylamino group, etc. are mentioned.

Specific examples of the C _1-8 alkyl group having a substituent include a chloromethyl group, a methoxymethyl group, a methylthiomethyl group, a methylsulfonylmethyl group, a dimethylaminomethyl group, a trichloromethyl group, a trifluoromethyl group, and 2-chloroethyl. Groups and the like.

Specific examples of the C _2-8 alkenyl group having a substituent include 2-chloroethenyl group, 2-fluoroethenyl group, 3,3,3-trifluoro-1-pentenyl group, 1,2,2-trifluoroethene. Examples thereof include a tenenyl group, a 2,3,3-trifluoro-2-propenyl group, a 2,3,3-triiodo-2-propenyl group, and a 2-methoxyethenyl group.

Specific examples of the C _2-8 alkynyl group having a substituent include 2-chloroethynyl group, 2-fluoroethynyl group, 3-fluoro-1-propynyl group, and 3,3,3-trifluoro-1-propynyl group. , 3-fluoro-2-propynyl group, 3-iodo-2-propynyl group and the like.

  Specific examples of the heterocyclic group having a substituent include 3-trifluoromethylpyridin-2-yl group, 4-trifluoromethoxy-2-pyridyl group, 3-methyl-1-pyrazolyl group, and 4-trifluoromethyl. Examples include a -1-imidazolyl group and a 3,4-difluoropyrrolidino group.

As ^{R, C OR 1, COR 1} , S (O) m R 1 and CO ₂ R ¹ in R ¹ is an unsubstituted of or an amino group having a substituent group, an unsubstituted or substituted _{1- 8} alkyl groups, unsubstituted or substituted C _3-8 cycloalkyl groups, unsubstituted or substituted C _2-8 alkenyl groups, unsubstituted or substituted C _2-8 alkynyl groups, It represents an unsubstituted or substituted aryl group, or an unsubstituted or substituted heterocyclic group. M represents an integer of 0 to 2.

R ¹ is an unsubstituted or substituted amino group, an unsubstituted or substituted C _1-8 alkyl group, an unsubstituted or substituted C _2-8 alkenyl group, unsubstituted or _{Examples of the} C _2-8 alkynyl group having a substituent, an unsubstituted or substituted aryl group, and an unsubstituted or substituted heterocyclic group are the same as those described in the description of R above. Can be mentioned.

Examples of the unsubstituted C _3-8 cycloalkyl group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group.
In addition, the “substituent” in the C _3-8 cycloalkyl group having a substituent as R ¹ is shown as the “substituent” in the aryl group having a substituent in X within a chemically acceptable range. The same thing as what was done can be mentioned.

Specific examples of OR ¹ include methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, s-butoxy group, i-butoxy group, t-butoxy group, methoxymethoxy group, ethoxymethoxy Group, methoxyethoxy group, ethoxyethoxy group, vinyloxy group, 1-propenyloxy group, 2-propenyloxy group, ethynyloxy group, 1-propynyloxy group, 2-propynyloxy group, aminooxy group, methylaminooxy group, Diethylaminooxy group, methoxycarbonylaminooxy group, phenoxy group, trichloromethoxy group, trifluoromethoxy group, difluoromethoxy group, 2,2,2-trifluoroethoxy group, pentafluoroethoxy group, 2-fluoroethoxy group, etc. It is done.

Specific examples of S (O) _m R ¹ include dimethylaminothio group, chloromethylthio group, 3-butenylthio group, ethynylthio group, 3-methylphenylthio group, methylsulfinyl group, ethylsulfinyl group, 1-butenylsulfinyl. Group, 1-hexynylsulfinyl group, 2,3-dimethylphenylsulfinyl group, methylsulfonyl group, dimethylaminosulfonyl group, N-ethyl-N-methylaminosulfonyl group, n-hexylsulfonyl group, 2-methyl-2- Examples include butenylsulfonyl group, 2-propynylsulfonyl group, 2-naphthylsulfonyl group, phenylsulfonyl group, 2-nitrophenylsulfonyl group, p-tolylsulfonyl group and the like.

Specific examples of COR ¹ include acetyl group, benzoyl group, propanoyl group, i-propylcarbonyl group, t-butylcarbonyl group, cyclopropylcarbonyl group, cyclobutylcarbonyl group, cyclopentylcarbonyl group, vinylcarbonyl group, 1-propenyl. Carbonyl group, 2-propenylcarbonyl group, i-propenylcarbonyl group, 1-propynylcarbonyl group, 2-propynylcarbonyl group, 3-butenylcarbonyl group, methylaminocarbonyl group, dimethylaminocarbonyl group, N-methyl-N- Examples include ethylaminocarbonyl group, aziridinocarbonyl group, azetidinocarbonyl group, pyrrolidinocarbonyl group, piperidinocarbonyl group, morpholinocarbonyl group, piperazinocarbonyl group, N-methylpiperazinocarbonyl group and the like. It is.

Specific examples of CO ₂ R ¹ include a methoxycarbonyl group, a trifluoromethoxycarbonyl group, a 1-pentenyloxycarbonyl group, a 2-propynyloxycarbonyl group, a phenoxycarbonyl group, and the like.

Of these, R is preferably a halogen atom, an unsubstituted or substituted amino group, a C _1-8 alkyl group, OR ¹ , and SR ¹ , and an unsubstituted or substituted amino group, C More preferred are _1-8 alkyl groups, OR ¹ , and SR ¹ .
As an unsubstituted or substituted amino group, an amino group (NH ₂ group) and a dialkylamino group are preferable, a C _1-8 alkyl group is preferably a C _1-4 alkyl group, and OR ¹ is C _{1- A 4-} alkoxy group is preferred, and SR ¹ is preferably a C _1-4 alkylthio group.

  n2 represents an integer of 0 to 3. n2 is preferably 0. When n2 is 2 or more, the plurality of Rs may be the same as or different from each other.

In formula (5), R ¹¹ represents a hydrogen atom, a halogen atom, a cyano group, a nitro group, a hydroxyl group, a thiol group, a formyl group, a carboxyl group, an unsubstituted or substituted amino group, an unsubstituted or substituted group. A C _1-8 alkyl group having a group, an unsubstituted or substituted C _2-8 alkenyl group, an unsubstituted or substituted C _2-8 alkynyl group, an unsubstituted or substituted aryl group Represents an unsubstituted or substituted heterocyclic group, OR ¹ , S (O) _m R ¹ , COR ¹ , or CO ₂ R ¹ , wherein R ¹ and m have the same meaning as described above. 〉.

R ¹¹ is a halogen atom, an unsubstituted or substituted amino group, an unsubstituted or substituted C _1-8 alkyl group, an unsubstituted or substituted C _2-8 alkenyl group, A substituted or substituted C _2-8 alkynyl group, an unsubstituted or substituted aryl group, an unsubstituted or substituted heterocyclic group, OR ¹ , S (O) _m R ¹ , COR ¹ , Or CO ₂ R ¹ may be the same as those described above for R.

In formula (4) and formula (5), Z represents a group represented by formula (a) or formula (b).
In formula (a), Q ¹ represents an unsubstituted or substituted alkyl group, an unsubstituted or substituted aralkyl group, an unsubstituted or substituted alkoxy group, an unsubstituted or substituted group. An aralkyloxy group having an unsubstituted or substituted alkylthio group, an unsubstituted or substituted aralkylthio group, or NR ²⁰ R ²¹ . R ²⁰ and R ²¹ are each independently a hydrogen atom, an unsubstituted or substituted alkyl group, an unsubstituted or substituted aralkyl group, or an unsubstituted or substituted aryl group. Represent.
In formula (b), Q ² represents an unsubstituted or substituted alkylthio group, an unsubstituted or substituted aralkylthio group, or NR ³⁰ R ³¹ . R ³⁰ and R ³¹ are each independently a hydrogen atom, an unsubstituted or substituted alkyl group, an unsubstituted or substituted aralkyl group, an unsubstituted or substituted alkoxy group, It represents a substituted or substituted aryl group, a sulfonyl group, an unsubstituted or substituted amino group, or COR ¹ , and R ³⁰ and R ³¹ may form a ring together. R ¹ represents the same meaning as described above.

Examples of the alkyl group in formula (a) and formula (b) include methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, i-butyl group, s-butyl group, and t-butyl. Preferred examples include C _1-8 alkyl groups such as a group, n-pentyl group, and n-hexyl group.
Examples of the aralkyl group in the formula (a) and the formula (b) include a benzyl group and a phenethyl group.
Examples of the alkoxy group in the formulas (a) and (b) include methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, i-butoxy group, s-butoxy group, t-butoxy group. C _1-8 alkoxy groups such as a group and n-hexyloxy group are preferred.
Examples of the aralkyloxy group in the formula (a) include a benzyloxy group and a phenethyloxy group.
Examples of the alkylthio group in formula (a) and formula (b) include methylthio group, ethylthio group, n-propylthio group, i-propylthio group, n-butylthio group, i-butylthio group, s-butylthio group, t-butylthio group. A C _1-8 alkylthio group such as a group is preferred.
Examples of the aralkylthio group in the formula (a) and the formula (b) include a benzylthio group and a phenethylthio group.
Examples of the aryl group in the formula (a) and the formula (b) include a phenyl group, a 1-naphthyl group, and a 2-naphthyl group.
Examples of the sulfonyl group in the formula (b) include a hydroxysulfonyl group; an alkylsulfonyl group such as a methylsulfonyl group and an ethylsulfonyl group (preferably a C _1-8 alkylsulfonyl group); a phenylsulfonyl group, a 1-naphthylsulfonyl group, and the like. An arylsulfonyl group (preferably a C _6-10 arylsulfonyl group) and the like can be mentioned.
Examples of the amino group having a substituent in formula (b) include a methylamino group, a dimethylamino group, a t-butylamino group, a t-butylmethylamino group, a methylphenylamino group, a benzylamino group, and a t-butoxycarbonylamino group. Group, acetylamino group, benzoylamino group and the like.
Examples of COR ¹ in the formula (b) include an acetyl group, a benzoyl group, a 2-pyridylcarbonyl group, a t-butylcarbonyl group, and a cyclohexylcarbonyl group.
The “substituent” in the formula (a) and the formula (b) is the same as that shown as the “substituent” in the aryl group having a substituent in the X within a chemically acceptable range. Can be mentioned.
The group represented by the formula (a) or the formula (b) is an aralkyl group in which Q ¹ in the formula (a) is an aralkyloxy group, an alkoxy group having ₃ or more carbon atoms, an aralkylthio group, an alkylthio group, an oxy group, It is preferably a C ₄ or higher alkyl group or NR ²⁰ R ²¹ , or Q ² in the formula (b) is preferably an aralkylthio group, an alkylthio group, or NR ³⁰ R ³¹ .

  In the tetrazoyl oxime derivative of the present invention, when Z is a group represented by the formula (a) or the formula (b), it exhibits an excellent plant disease control effect that was not found in conventional tetrazoyl oxime derivatives. become. The structure of the group represented by the formula (a) is O-thiocarbamate, dithiocarbamate, thiourea, and thioamide, and the structure of the group represented by the formula (b) is S-thiocarbamate and urea. These groups always contain two or more nitrogen atoms and / or sulfur atoms. Although details are unclear, it is presumed that the nitrogen atom and / or sulfur atom in Z performs some action to exert the effect of the present invention.

  The tetrazoyl oxime derivative represented by the formula (1) has (E) and (Z) stereoisomers based on the carbon-nitrogen double bond of the oxime moiety. Both of these two stereoisomers and mixtures thereof are included in the present invention. Usually, the synthesized product is obtained only as the (Z) isomer or as a mixture of the (E) isomer and the (Z) isomer. Two isomers can be isolated by separating and purifying a mixture of the (E) isomer and the (Z) isomer by a known method such as silica gel column chromatography. Both the (Z) isomer and the (E) isomer have activity, and the (Z) isomer is preferred.

  The salt of the tetrazoyl oxime derivative of the present invention is a salt of the compound represented by the formula (1). The salt is not particularly limited as long as the salt is acceptable in agriculture and horticulture. For example, salts of inorganic acids such as hydrochloride, nitrate, sulfate, and phosphate; salts of organic acids such as acetate, lactate, propionate, and benzoate.

(Method for producing tetrazoyloxime derivative and salt thereof)
The tetrazoyl oxime derivative represented by the formula (1) can be produced, for example, according to the method described in JP2003-137875A or WO03 / 016303 pamphlet.

式（１）、（６）および（７）中、Ａ、Ｘ、Ｈｅｔ、およびｎ１は前記と同じ意味を表し、Ｌはハロゲン原子等の脱離基を表す。

In the formulas (1), (6) and (7), A, X, Het and n1 have the same meaning as described above, and L represents a leaving group such as a halogen atom.

  That is, by reacting the oxime represented by the formula (6) and the compound represented by the formula (7) in the presence of a base, the tetrazoyl oxime derivative of the present invention represented by the formula (1) is obtained. Can be obtained.

Examples of the base used in this reaction include inorganic bases such as sodium hydroxide, potassium hydroxide, sodium hydride, sodium carbonate, and potassium carbonate; triethylamine, 4- (dimethylamino) pyridine, pyridine, 1,8-diazabicyclo [5. 4.0] organic bases such as undecene-7, 1,5-diazabicyclo [4.3.0] nonene-5; and the like. These bases can be used alone or in combination of two or more.
The usage-amount of a base is 0.01-100 times mole normally with respect to the oxime represented by Formula (6), Preferably it is 0.1-5 times mole.

This reaction can be performed in the presence or absence of a solvent.
The solvent to be used is not particularly limited as long as it is an inert solvent for this reaction. For example, hydrocarbon solvents such as pentane, hexane, heptane, benzene, toluene, xylene; halogen solvents such as dichloromethane, chloroform, carbon tetrachloride; nitrile solvents such as acetonitrile, propiononitrile; diethyl ether, dioxane, tetrahydrofuran, etc. Ether solvents; amide solvents such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methylpyrrolidone; sulfoxide solvents such as dimethyl sulfoxide; water; and mixed solvents thereof; It is done.

  The temperature at the time of carrying out this reaction is usually -70 ° C to + 200 ° C, preferably -20 ° C to + 100 ° C. The reaction time is usually 30 minutes to 24 hours, although it depends on the reaction scale and the like.

  Moreover, the salt of the compound represented by Formula (1) can be manufactured by making an acid act on the compound represented by Formula (1) according to a conventional method.

  When Het in the compound represented by the formula (7) is a pyridyl group represented by the formula (4) or a thiazoyl group represented by the formula (5), the reaction of the present invention is directly performed by the above reaction. A compound represented by the formula (1) can be obtained.

The tetrazoyl oxime derivative of the present invention and its salt are reacted in the same manner as described above using a compound represented by formula (8) or formula (9) instead of the compound represented by formula (7), A compound into which an amino-substituted pyridine group or an amino-substituted thiazoyl group is introduced can be obtained, and can be produced by replacing the amino group with Z as described above. In the formula (8) or formula (9), R ⁴⁰ and R ⁴¹ are substituents such as a hydrogen atom and an alkyl group.

Examples of the method for substituting the amino group (NR ⁴⁰ R ⁴¹ ) with Z described above include (1) converting the amino group to a phenoxycarbonylamino group by reacting the amino group with a haloformate phenyl ester, etc. (2) Amino group is reacted with a carboxylic acid, acid chloride, etc. to convert it to an amide group, and a sulfurizing reagent such as phosphorus pentasulfide is added to the amino group to react with urea group or S-thiocarbamate group. (3) Amino group is reacted with phosgene, thiophosgene, etc. to convert to an isocyanate group, isothiocyanate group, and this is reacted with alcohol, amine, thiol, etc. Examples thereof include a thiocarbamate, a thiourea group, and a method for converting to a urea group.

  In any of the above reactions, the target compound represented by the formula (1) and a salt thereof can be isolated by performing a general post-treatment operation after the reaction is completed. In addition, if purification of the product is necessary, known and conventional purification means such as distillation, recrystallization or column chromatography can be employed.

Tetrazoyl oxime derivatives represented by the formula (1) or salts thereof (hereinafter sometimes referred to as “compounds of the present invention”) are a wide variety of filamentous fungi, such as Oomycetes, offspring It has excellent bactericidal activity against bacteria belonging to (sac) fungi (Ascomycetes), incomplete fungi (Deuteromycetes), and basidiomycetes.
Therefore, the composition comprising the compound of the present invention as an active ingredient is used for the control of various diseases that occur during the cultivation of agricultural and horticultural crops including flower buds, turf and grass, by seed treatment, foliage application, soil application or water surface application, etc. Can be used.

  For example, sugar beet: brown spot disease (Cercospora beticola), black root disease (Aphanomyces cochlioides); groundnut: brown spot disease (Mycosphaerella arachidis); black astringency (Mycosphaerella berkeleyi); (Mycosphaerella melonis), mycorrhizal disease (Sclerotinia sclerotiorum), gray mold (Botrytis cinerea), black rot (Cladosporium cucumerinum), downy mildew (Pseudoperonospora cubensis); tomato: gray mold (Botrytis cinerea), leaf mold ( Cladosporium fulvum), cotton rot (Phythium aphanidermatum), plague (Phytophthora infestans); eggplant: gray mold (Botrytis cinerea), black blight (Corynespora melongenae), powdery mildew (Erysiphe cichoracearum); spinach disease (Pythium ultimum); Strawberry: Botrytis cinerea, powdery mildew (Sphaerotheca aphanis); Onion: Gray rot (Botrytis allii) , Gray mold disease (Botrytis cinerea); kidney beans: Sclerotinia sclerotiorum; gray mold disease (Botrytis cinerea); apples: powdery mildew (Podosphaera leucotricha); black star disease (Venturia inaequalis); monilinia mali disease (Monilinia mali) ;

  Oysters: powdery mildew (Phyllactinia kakicola), anthracnose (Gloeosporium kaki), horn spot leaf disease (Cercospora kaki); peach sweet cherry: Monilinia fructicola; grapes: gray mold disease (Botrytis cinerea), powdery mildew Uncinula necator, late rot (Glomerella cingulata), downy mildew (Plasmopara viticola); pear: black rot (Venturia nashicola), red scab (Gymnosporangium asiaticum); Spot disease (Pestalotia theae), anthracnose (Colletotrichum theae-sinensis); Citrus: Elderly fawcetti, blue mold (Penicillium italicum), green mold (Penicillium digitatum), gray mold (Botrytis cinerea); Barley: powdery mildew (Erysiphe graminis f.sp.hordei), naked smut (Ustilago nuda);

  Wheat: Red mold disease (Gibberella zeae), Red rust disease (Puccinia recondita), Spot disease (Cochliobolus sativus), Dry blight (Leptosphaeria nodorum), Eye spot disease (Pseudocercosporella herpotrichoides), Powdery mildew (Erysiphe graminis f.sp. tritici), red snow rot (Micronectriella nivalis), brown snow rot (Pythium iwayamai); rice: rice blast (Pyricularia oryzae), blight (Rhizoctonia solani), idiotic seedling (Gibberella fujikuroi), sesame leaf blight (Cochliobolus niyabeanus), seedling blight (Pythiym graminicolum); soybean: purpura (Cercospora kikuchii), downy mildew (Peronospora manshurica), stem blight (Phytophthora sojae); potato: Phytophthora infestans; Tuberculosis (Plasmodiophora brassicae); Tobacco: Sclerotinia sclerotiorum; Powdery mildew (Erysiphe cichoracearum); Tulip: Gray mold (Botrytis cinerea); S: snow mold large Rot (Sclerotinia borealis), red grilled disease (Pythium aphanidermatum); orchard grass: Powdery mildew can be used (Erysiphe graminis) controlling such.

  In recent years, various pathogenic bacteria have developed resistance to phenylamide fungicides, strobilurin fungicides and the like, resulting in insufficient efficacy of these drugs, and drugs effective against resistant bacteria are desired. The compound of the present invention is a drug having an excellent bactericidal effect not only for pathogenic bacteria sensitive to these drugs but also for resistant bacteria.

For example, the compounds of the present invention are effective against Phytophthora infestans, cucumber downy mildew (Pseudoperonospora cubensis), and downy mildew (Plasmopara viticola), which are resistant to metalaxyl. is there.
Furthermore, cucumber downy mildew (Pseudoperonospora cubensis) and resistance to grape downy mildew (Plasmopara viticola) that are resistant to strobilurin fungicides (eg, cresoxime methyl, azoxystrobin, etc.) The compound is effective.
Preferable diseases that can be applied include Plasmopara viticola, Pseudoperonospora cubensis, Phytophthora infestans, Pythium aphanidermatum, and sugar beet black root There are various diseases caused by oomycetes such as Aphanomyces cochlloides.

The compound of the present invention can also be used as an antifouling agent for preventing aquatic organisms from adhering to underwater contact objects such as ship bottoms and fish nets.
Some intermediates produced in the production process of the compound of the present invention exhibit bactericidal activity.
Furthermore, the compound of the present invention can be used as an antibacterial and antifungal agent for walls, bathtubs, shoes and clothes by mixing in paints and fibers.

2) Plant disease control agent The plant disease control agent of this invention contains at least 1 sort (s) chosen from the tetrazoyl oxime derivative or its salt represented by Formula (1) as an active ingredient.
The plant disease control agent of the present invention may be in a form consisting only of the compound of the present invention, or a form that can be taken by a general agricultural chemical, that is, a wettable powder, a granule, a powder, an emulsion, an aqueous solvent, a suspension. It may be in the form of a flowable or the like.

  In the plant disease control agent of the present invention, when it is intended as a solid agent, as an additive and / or carrier, vegetable powder such as soybean flour, wheat flour, diatomaceous earth, apatite, gypsum, talc, bentonite, pyrophyll Mineral fine powders such as light and clay, and organic and inorganic compounds such as sodium benzoate, urea, and sodium sulfate can be used.

  For liquid dosage forms, petroleum fractions such as kerosene, xylene and solvent naphtha, cyclohexane, cyclohexanone, dimethylformamide, dimethyl sulfoxide, alcohol, acetone, trichloroethylene, methyl i-butyl ketone, mineral oil Vegetable oil, water or the like can be used as a solvent.

  Furthermore, in the plant disease control agent of this invention, in order to take a uniform and stable form in these formulations, a surfactant can be added as necessary.

  Examples of the surfactant to be used include alkyl phenyl ether added with polyoxyethylene, alkyl ether added with polyoxyethylene, higher fatty acid ester added with polyoxyethylene, sorbitan higher fatty acid ester added with polyoxyethylene, polyoxyethylene Nonionic surfactants such as tristyryl phenyl ether added with oxyethylene; sulfate ester salt of alkylphenyl ether added with polyoxyethylene, alkyl benzene sulfonate, sulfate ester of higher alcohol, alkyl naphthalene sulfonate, Examples include polycarboxylates, lignin sulfonates, alkyl naphthalene sulfonate formaldehyde condensates, i-butylene-maleic anhydride copolymers, and the like.

  The amount of the active ingredient in the preparation is not particularly limited, but is usually 0.5 to 95% by mass, preferably 2 to 70% by mass with respect to the entire composition (preparation).

  When the plant disease control agent of the present invention is a wettable powder, emulsion, or flowable agent, it can be diluted with water to a predetermined concentration and used as a suspension or emulsion. Moreover, when it is a powder agent and a granule, it can be used by the method of spraying to a plant as it is.

  It goes without saying that the compound of the present invention or the plant disease control agent of the present invention alone is sufficiently effective, but it is mixed with one or more of various fungicides, insecticides, acaricides, or synergists. Can also be used.

  Typical examples of fungicides, insecticides, acaricides, and plant growth regulators that can be used in combination with the compound of the present invention or the plant disease control agent of the present invention are shown below.

<Fungicide>
Copper agent; basic copper chloride, basic copper sulfate and the like. Sulfur agent; thiuram, dineb, manneb, mancozeb, ziram, propineb, polycarbamate, etc. Polyhaloalkylthio agents; captan, phorpet, dichlorofluanide, etc. Organochlorine agents; chlorothalonil, fusalide, etc. Organophosphorus agent; IBP, EDDP, triclofosmethyl, pyrazophos, fosetyl and the like. Benzimidazole agents; thiophanate methyl, benomyl, carbendazim, thiabendazole and the like. Dicarboximide agents; iprodione, procymidone, vinclozolin, fluorimide, etc. Carboxamide agents; oxycarboxin, mepronil, flutolanil, teclophthalam, trichlamide, pencyclon and the like. Acylalanine agents; metalaxyl, oxadixyl, furaxyl and the like. Strobilurin-based agents; azoxystrobin, cresoxime methyl, pyraclostrobin, trifloxystrobin, pyribencarb, famoxadone, fenamidone and the like.

  Anilinopyrimidine agents; and purine, mepanipyrim, pyrimethanil, diprodinil and the like. SBI agents; triadimephone, triadimenol, vitertanol, microbutanyl, hexaconazole, propiconazole, triflumizole, prochloraz, pefazoate, phenalimol, pyrifenox, trifolin, flusilazole, etaconazole, diclobutrazole, fluotrimazole, Flutriaphen, penconazole, diniconazole, imazalyl, tridemorph, fenpropimorph, butiobate, epoxiconazole, metconazole, prothioconazole, spiroxamine, fenhexamide, pyributycarb, etc.

  Antibiotic agents; polyoxins, blasticidin S, kasugamycin, validamycin, dihydrostreptomycin sulfate, etc. Anilide agents; boscalid, pentiopyrad, fluopyram, bixaphene, etc. Guanidine-based agents: iminoctadine acetate, iminoctadine arbesylate, dodine, guazatine and the like. Valine-based agents; dimethomorph, fulmorph, iprovaricarb, benchavaricarb, mandipropamide and the like.

  Other fungicides; simoxanil, cyazofamide, amisulbrom, propamocarb, fluazinam, propamocarb acetate, ethaboxam, fluopicolide, zoxamide, cyfluphanamide, metolaphenone, proquinadide, hydroxyisoxazole, metasulfocarb, anilazine, isoprothiolane, propimizone, propenazole , Acibenzoral S methyl, isothianyl, pyroxylone, phthalide, tricyclazole, carpropamide, phenoxanyl, diclocimet, fluazinam, fludioxonil, pyrrolnitrin, hydroxyisoxazole, fursulfamide, dietofencarb, quintozene, metasulfocarb, anilazine, quinomethionate dinodibutin, dithianone , Oki Clinic acid, lecithin, baking soda, Fenaminosurufu, phenazine oxide, and the like.

<Insecticide / Acaricide>
Organic phosphorus and carbamate insecticides; fenthion, fenitrothion, diazinon, chlorpyrifos, ESP, bamidthione, phentoate, dimethoate, formone, marathon, trichlorphone, thiomethone, phosmet, dichlorvos, acephate, EPBP, methylparathion, oxydimethone methyl, ethion, thione Cyanophos, isoxathione, pyridafenthion, hosalon, methidathion, sulprophos, chlorfenvinphos, tetrachlorbinphos, dimethylvinphos, propaphos, isofenphos, ethylthiomethone, propenophos, pyraclophos, monocrotophos, azinephosmethyl, aldicarb, mesomil, thiodicarb, carbofuran, Carbosulfan, Benfuracarb, Fracio Lube, propoxur, BPMC, MTMC, MIPC, carbaryl, pirimicarb, ethiofencarb, fenoxycarb, and the like.

  Pyrethroid insecticides; permethrin, cypermethrin, deltamethrin, fenvalerate, fenpropatoline, pyrethrin, allethrin, tetramethrin, resmethrin, dimethrin, proprasrin, phenothrin, protorin, fluvinate, cyfluthrin, cyhalothrin, flucitrinate, etofenprox, Cycloprotonline, trolamethrin, silafluophene, brofenprox, acrinusrin and the like.

  Benzoylurea and other insecticides; diflubenzuron, chlorfluazuron, hexaflumuron, triflumuron, tetrabenzuron, flufenoxuron, flucycloxuron, buprofezin, pyriproxyfen, metoprene, benzoepin, diafenthiuron, acetamiprid Microbial pesticides such as imidacloprid, nitenpyram, fipronil, cartap, thiocyclam, bensultap, nicotine sulfate, rotenone, metaldehyde, emamectin, fulvendiamide, spinosad, machine oil, BT and entomopathogenic virus.

  Nematicides; phenamifos, phostiazates, etc. Acaricides; chlorbenzilate, phenisobromolate, dicophore, amitraz, BPPS, benzomate, hexothiazox, fenbutazin oxide, polynactin, quinomethionate, CPCBS, tetradiphone, avermectin, milbemectin, clofentezin, cihexatin, pyridaben, fenpyroximate, tebufenpyrad, Pyrimidifen, phenothiocarb, dienochlor, fluacrylpyrim and the like.

<Plant growth regulator>
Gibberellins (eg, gibberellin A3, gibberellin A4, gibberellin A7), IAA, NAA and the like.

  Next, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the examples.

Example 1
[(Z)-(1-Methyl-1H-tetrazol-5-yl) phenylmethanone-O- {2-[(N-methoxy-N-methylaminocarbonyl) amino] pyridin-6-ylmethyl} -oxime Manufacturing)
(Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- (2-aminopyridine-6) is obtained by steps i to ii according to the method described in JP-A-2003-137875. -Ilmethyl) -oxime was obtained. That is,
[Step i]
(1-Methyltetrazol-5-yl) phenylmethanone (59.1 mmol) and hydroxylammonium chloride (148 mmol) were added to 100 ml of pyridine, followed by stirring at 45 ° C. for 24 hours. After completion of the reaction, the reaction solution was concentrated under reduced pressure, and water and ethyl acetate were added to the resulting residue to extract the reaction product. The organic layer was washed successively with dilute hydrochloric acid, water and aqueous sodium hydrogen carbonate solution, and then the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off from the organic layer to obtain (1-methyltetrazol-5-yl) phenylmethanone oxime (yield 100%).

[Step ii]
1.40 g (60% in oil) of sodium hydride was suspended in 30 ml of dry N, N-dimethylformamide. While cooling in an ice bath, a solution consisting of 12.6 mmol of (1-methyltetrazol-5-yl) phenylmethanone oxime and 15 ml of dry N, N-dimethylformamide was added dropwise. After stirring for 10 minutes, 14 mmol of 2-bromomethyl-6-aminopyridine dissolved in 15 ml of dry N, N-dimethylformamide was further added dropwise. After completion of dropping, the ice bath was removed and stirring was continued for 1.5 hours. The reaction solution was poured into saturated aqueous ammonium chloride, and the reaction product was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, and then the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off from the organic layer, and the obtained residue was purified using silica gel column chromatography to obtain (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- ( 2-Aminopyridin-6-ylmethyl) -oxime was obtained.

[Step iii]
(Z)-(1-Methyl-1H-tetrazol-5-yl) phenylmethanone-O- (2-aminopyridin-6-ylmethyl) -oxime 5.59 g (18.07 mmol) and 1.79 g of pyridine (22 .58 mmol) was dissolved in methylene chloride (80 mL), and a solution of phenyl chloroformate (3.53 g, 22.58 mmol) in methylene chloride (50 mL) was added dropwise at 0 ° C. over 1 hour and then stirred at room temperature for 18 hours. . Methylene chloride (200 mL) and water (100 mL) were added to the reaction mixture, the organic layer was washed with saturated brine, dried over magnesium sulfate, and then concentrated under reduced pressure. The obtained crude product was purified by silica gel column chromatography (eluent; hexane: ethyl acetate = 4: 1 (v / v)) to obtain (Z)-(1-methyl-1H-tetrazol-5-yl). 6.12 g of phenylmethanone-O- [2- (phenoxycarbonylamino) pyridin-6-ylmethyl] -oxime was obtained.

[Step iv]
Then, 0.21 g (0.49 mmol) of (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- [2- (phenoxycarbonylamino) pyridin-6-ylmethyl] -oxime 0.10 g (1.00 mmol) of N, O-dimethylhydroxylamine hydrochloride was dissolved in tetrahydrofuran (5 mL), and 0.16 g (1.05 mmol) of 1,8-diazabicyclo [5.4.0] undec-7-ene was dissolved. ) And stirred at room temperature overnight. The reaction solution was concentrated under reduced pressure, and the resulting crude product was purified by silica gel column chromatography (eluent; hexane: ethyl acetate = 2: 1 (v / v)) to give (Z)-(1-methyl-1H -Tetrazol-5-yl) Phenylmethanone-O- {2-[(N-methoxy-N-methylaminocarbonyl) amino] pyridin-6-ylmethyl} -oxime 0.08 g was obtained.

Example 2
[Production of (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- [2- (benzylthioxycarbonylamino) pyridin-6-ylmethyl] -oxime]
[Steps i to iii]
In the same manner as in Example 1, (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- [2- (phenoxycarbonylamino) pyridin-6-ylmethyl] -oxime was prepared. .

[Step iv]
Then, 0.21 g (0.49 mmol) of (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- [2- (phenoxycarbonylamino) pyridin-6-ylmethyl] -oxime 0.12 g (1.00 mmol) of benzylthiol was dissolved in tetrahydrofuran (5 mL), and 0.09 g (0.59 mmol) of 1,8-diazabicyclo [5.4.0] undec-7-ene was added at room temperature. Stir overnight. The reaction solution was concentrated under reduced pressure, and the resulting crude product was purified by silica gel column chromatography (eluent; hexane: ethyl acetate = 4: 1 (v / v)) to give (Z)-(1-methyl-1H -Tetrazol-5-yl) Phenylmethanone-O- [2- (benzylthioxycarbonylamino) pyridin-6-ylmethyl] -oxime 0.03 g was obtained.

Example 3
[Production of (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- {2- (pentanethiocarbonyl) amino] pyridin-6-ylmethyl} -oxime]

[Step i]
In the same manner as in Example 1, (1-methyltetrazol-5-yl) phenylmethanone oxime was produced.
[Step ii]
1.40 g (60% in oil) of sodium hydride was suspended in 30 ml of dry N, N-dimethylformamide. While cooling in an ice bath, a solution consisting of 12.6 mmol of (1-methyltetrazol-5-yl) phenylmethanone oxime and 15 ml of dry N, N-dimethylformamide was added dropwise. After stirring for 10 minutes, 14 mmol of 2-bromomethyl-6- (hexanoylamino) pyridine dissolved in 15 ml of dry N, N-dimethylformamide was further added dropwise. After completion of dropping, the ice bath was removed and stirring was continued for 1.5 hours. The reaction solution was poured into saturated aqueous ammonium chloride, and the reaction product was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, and then the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off from the organic layer, and the obtained residue was purified using silica gel column chromatography to obtain (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O— { 2- (Pentanecarbonyl) amino] pyridin-6-ylmethyl} -oxime was obtained.

[Step iii]
(Z)-(1-Methyl-1H-tetrazol-5-yl) phenylmethanone-O- {2- (pentanecarbonyl) amino] pyridin-6-ylmethyl} -oxime (0.41 g, 1.00 mmol) , 4-Dioxane (20 mL), 0.44 g (1.1 mmol) of Lawson's reagent was added, and the mixture was heated to reflux for one day. After cooling, ethyl acetate was added and the mixture was washed with water and saturated brine. Magnesium sulfate was added to the organic layer, dried and concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (eluent; benzene: ethyl acetate = 20: 1 (v / v)) and purified (Z )-(1-Methyl-1H-tetrazol-5-yl) Phenylmethanone-O- {2- (pentanethiocarbonyl) amino] pyridin-6-ylmethyl} -oxime 0.15 g was obtained.

Example 4
[Production of (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- [2- (methoxythiocarbonylamino) pyridin-6-ylmethyl] -oxime]
[Steps i to ii]
In the same manner as in Example 1, (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- (2-aminopyridin-6-ylmethyl) -oxime was prepared.

[Step iii]
Ice-cooled (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- (2-aminopyridin-6-ylmethyl) -oxime 0.40 g (1.29 mmol) in acetone (6 mL) ) · Chloroform (3 mL) mixed solvent was added thiophosgene 0.18 g (1.56 mmol) and saturated aqueous sodium hydrogen carbonate (3 mL), and the mixture was stirred as it was for 30 minutes. The solution was concentrated under reduced pressure, extracted with methylene chloride, the organic layer was washed with saturated brine, dried by adding magnesium sulfate, and then evaporated under reduced pressure to give crude (Z)-(1-methyl-1H-tetrazole. -5-yl) Phenylmethanone-O- (2-isothiocyanatopyridin-6-ylmethyl) -oxime (0.53 g) was obtained.

[Step iv]
(Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- (2-isothiocyanatopyridin-6-ylmethyl) -oxime 0.20 g (0.57 mmol) in methanol (10 mL) And heated to reflux overnight. The solvent was distilled off under reduced pressure, and the resulting crude product was purified by silica gel column chromatography (eluent; hexane: ethyl acetate = 2: 1 (v / v)) to give (Z)-(1-methyl-1H -Tetrazol-5-yl) 0.14 g of phenylmethanone-O- [2- (methoxythiocarbonylamino) pyridin-6-ylmethyl] -oxime was obtained.

Example 5
[(Z)-(1-Methyl-1H-tetrazol-5-yl) phenylmethanone-O- {2-[(N-benzyl-N-methylaminothiocarbonyl) amino] pyridin-6-ylmethyl} -oxime Manufacturing of〕
[Steps i to iii]
In the same manner as in Example 4, (Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- (2-isothiocyanatopyridin-6-ylmethyl) -oxime was prepared.

[Step iv]
(Z)-(1-methyl-1H-tetrazol-5-yl) phenylmethanone-O- (2-isothiocyanatopyridin-6-ylmethyl) -oxime 1.40 g (3.24 mmol) was added to benzene (25 mL). And stirred at room temperature overnight. The solvent was distilled off under reduced pressure, and the resulting crude product was purified by silica gel column chromatography (eluent; hexane: ethyl acetate = 2: 1 (v / v)) to give (Z)-(1-methyl-1H -Tetrazol-5-yl) 1.65 g of phenylmethanone-O- {2-[(N-benzyl-N-methylaminothiocarbonyl) amino] pyridin-6-ylmethyl} -oxime was obtained.

Example 6
Other examples of the tetrazoyl oxime derivative of the present invention that can be produced by the above method are shown in Tables 1 to 5. In Table 1, Z represents Z in chemical formula (I). Z in Table 2 represents Z in chemical formula (II). Z in Table 3 represents Z in the chemical formula (III). Z in Table 4 represents Z in the chemical formula (IV). Z in Table 5 represents Z in chemical formula (V). Table 6 shows the physical properties and ¹ H-NMR of some of the compounds shown in Tables 1 to 5. The unit of melting point is ° C. VISC. OIL indicates a viscous oil and AMR indicates amorphous. ND20.2 1.6092 indicates that the refractive index at 20.2 ° C. is 1.6092.

  Tables 1 to 5 only show some of the tetrazoyl oxime derivatives of the present invention that can be produced by the above-described methods. It is described in the present specification that other compounds not specifically shown in the present specification, that is, those substituted with various groups that do not depart from the spirit and scope of the present invention can be produced and used by the above-described methods and the like. It can be easily understood by those skilled in the art.

Next, some preparation examples of the plant disease control agent of the present invention will be shown. However, the additives and addition ratios are not limited to these examples, and can be changed in a wide range.
The part in a formulation example shows a mass part.

Formulation Example 1 Wetting agent Compound of the present invention 40 parts Clay 53 parts Dioctyl sulfosuccinate sodium salt 4 parts Lignin sulfonic acid sodium salt 3 parts The above is uniformly mixed and finely pulverized to hydrate 40% active ingredient. Get the agent.

Formulation Example 2 Emulsion Compound of the present invention 10 parts Solvesso 200 53 parts Cyclohexanone 26 parts Calcium dodecylbenzenesulfonate 1 part Polyoxyethylene alkylallyl ether 10 parts The above components are mixed and dissolved to obtain an emulsion containing 10% active ingredient.

Formulation Example 3 Powder A compound of the present invention 10 parts Clay 90 parts The above is uniformly mixed and finely pulverized to obtain a powder of 10% active ingredient.

Formulation Example 4 Granules Compound of the present invention 5 parts Clay 73 parts Bentonite 20 parts Dioctylsulfosuccinate sodium salt 1 part Potassium phosphate 1 part After pulverizing and mixing well, adding water and kneading well, granulation drying As a result, granules containing 5% of the active ingredient are obtained.

Formulation Example 5 Suspension Compound of the present invention 10 parts Polyoxyethylene alkyl allyl ether 4 parts Polycarboxylic acid sodium salt 2 parts Glycerin 10 parts Xanthan gum 0.2 parts Water 73.8 parts To obtain a suspension containing 10% of the active ingredient.

Formulation Example 6 Granule wettable powder Compound of the present invention 40 parts Clay 36 parts Potassium chloride 10 parts Alkylbenzenesulfonic acid sodium salt 1 part Lignin sulfonic acid sodium salt 8 parts Formaldehyde condensate of alkylbenzenesulfonic acid sodium salt 5 parts After finely pulverizing, add an appropriate amount of water and knead to make a clay. The clay-like product is granulated and then dried to obtain a granule wettable powder containing 40% of the active ingredient.

(Test Example) Tomato plague (PN) control test Tomato seedlings (variety “Regina”, 4-5 leaf stage) cultivated in an unglazed pot were sprayed with the emulsion of Formulation Example 2 at a concentration of 100 ppm active ingredient. After spraying, it was naturally dried at room temperature, sprayed with a zoospore suspension of Phytophthora infestans, and kept for 4 days in a high-humidity constant temperature room (20 ° C.) repeating light and dark every 12 hours. The lesion appearance state on the leaf was compared with no treatment, and the control effect (control value) was obtained.

Compound Nos. A-11, a-41, a-43, a-44, a-45, a-51, a-62, a-63, a-64, a-65, a-66, a-81, a-82, a-83, a-84, a-104, a-106, a-111, a-118, a-119, a-120, a-121, a-189, a-58, a- 59, a-61, a-80, a-601, a-14, a-15, a-311, a-13, a-314, a-39, and a-54 were subjected to a PN control test. As a result, the control value was 70% or more. The compound numbers correspond to the compound numbers in Table 1.
Control value [%]
= [(Severity of untreated section-Severity of treated section) / (Severity of untreated section)] × 100

  As described above, in the tetrazoyl oxime derivative and the salt thereof of the present invention, if Z is a group represented by the formula (a) or the formula (b), even if the group of other parts is changed, Although it is strong and weak, it can be seen that it exhibits a control effect against plant diseases.

Claims (3)

Formula (1):

[In Formula (1),
Het is the formula (4):

(In formula (4),
Z is the formula (a):

<In the formula (a), Q ¹ represents an alkoxy group having unsubstituted or substituted group, unsubstituted A Rarukiruokishi group, an unsubstituted of A alkylthio group, an unsubstituted A Rarukiruchio group or NR ²⁰ R ^21, . R ²⁰ and R ²¹ each independently represents a hydrogen atom, an unsubstituted or substituted alkyl group, an unsubstituted or substituted aralkyl group, or an unsubstituted or substituted aryl group. >
Or formula (b):

<In Formula (b), Q ² represents an unsubstituted or substituted aralkylthio group, or NR ³⁰ R ³¹ . R ³⁰ and R ³¹ are each independently an unsubstituted or substituted alkyl group, an unsubstituted or substituted aralkyl group, an unsubstituted or substituted alkoxy group, an unsubstituted or substituted group Represents an aryl group having a substituent, a sulfonyl group, an unsubstituted or substituted amino group, or COR ¹ , and R ³⁰ and R ³¹ may be combined to form a ring. However, the case where R ³⁰ and R ³¹ are simultaneously an unsubstituted or substituted alkyl group is excluded. R ¹ is an unsubstituted or substituted amino group, an unsubstituted or substituted C _1-8 alkyl group, an unsubstituted or substituted C _3-8 cycloalkyl group, unsubstituted or A C _2-8 alkenyl group having a substituent, an unsubstituted or substituted C _2-8 alkynyl group, an unsubstituted or substituted aryl group, or an unsubstituted or substituted heterocyclic group ; Represent. Represents a group represented by A pyridyl group represented by
] The tetrazoyl oxime derivative represented by these, and its salt. Q ¹ in the formula (a) is, aralkyloxy group, C ₃ or more alkoxy groups, aralkylthio group, an alkylthio group, young properly is NR ²⁰ R ^21, or Q ² in the formula (b), aralkylthio , tetrazolyl oxime derivative and a salt thereof according to claim 1 young properly is NR ³⁰ R ^31.   The plant disease control agent which contains at least 1 sort (s) chosen from the tetrazoyl oxime derivative or its salt of Claim 1 or 2 as an active ingredient.