JP2003040860A - Phthalamide derivative or salt thereof and agricultural /horticultural insecticide and method for using the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a phthalamide derivative (salt thereof) having high pest- controlling effect as an agricultural/horticultural insecticide and also similarly having high pest-controlling effect by the combined use with other agricultural/ horticultural insecticide, miticide, nematocide, fungicide, herbicide, plant growth regulator, biological pesticide, etc. SOLUTION: This phthalamide derivative (salt thereof) is shown by formula (I) [where, A<1> is a (substituted) alkylene, (substituted) 1-8C alkynylene, (substituted) 1-8C alkenylene or the like; R<1> is H, a (halo)cycloalkyl, (substituted) phenyl, (substituted) heterocyclic group, A<2> -R<4> or the like; R<2> and R<3> are each H, a cycloalkyl, A<2> -R<4> or the like; A<2> is C (=O), C (=S), C (=NR<5> ) or the like; R<4> is H, an alkyl, (substituted) phenyl, (substituted) heterocyclic group or the like; X and Y are each a halogen atom, cyano, nitro, a (substituted) phenyl, (substituted) heterocyclic group or the like; l is 0-4; m is 0-5; n is 0-2; excepting known compounds]. The agricultural/horticultural insecticide comprises the phthalamide derivative salt thereof) as the active ingredient. The method for using the insecticide is also provided.

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to a phthalamide derivative or a salt thereof, an agricultural and horticultural insecticide containing the compound as an active ingredient, and a method for using the insecticide.

[0002]

2. Description of the Related Art Japanese Unexamined Patent Publication (Kokai) No. 61-180753 discloses some compounds of the phthalamide derivative of the present invention, but neither describes nor suggests that they are useful as agricultural and horticultural insecticides. Further, JP-A-59-163353 and J. C. S. Perkin I, 1338-135
No. 0, (1978), etc., but no description or suggestion that they are useful as agricultural and horticultural insecticides is made at all.

[0003]

DISCLOSURE OF THE INVENTION The inventors of the present invention have conducted extensive studies to develop new agricultural and horticultural chemicals, and as a result, the phthalamide derivative represented by the general formula (I) of the present invention has not been described in the literature. The present invention has been completed by discovering a novel use as an agricultural and horticultural insecticide including a compound disclosed in the prior art, which is a novel compound.

[0004]

The present invention has the general formula (I)

[Chemical 3] {In the formula, A ¹ is a C ₁ -C ₈ alkylene group, which may be the same or different, and a halogen atom, a cyano group, a nitro group, a halo C _1-
C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, a hydroxy C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkylthio C ₁ -C ₆ alkyl group,

C ₁ -C ₆ alkoxycarbonyl group, phenyl group or the same or different, halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group , C ₁ -C ₆ alkylsulfonyl group, halo
_{1 selected from} C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino group which may be the same or different, or C ₁ -C ₆ alkoxycarbonyl group
1 selected from substituted phenyl groups having the above substituents
Substituted C ₁ -C ₈ alkylene group having the above substituents, C ₃ -C ₈
Alkenylene group, which may be the same or different, halogen atom, cyano group, nitro group, halo C ₁ -C ₆ alkyl group, C _1-
C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, C ₁ -C ₆ alkylthio C ₁ -C ₆ alkyl group,

C ₁ -C ₆ alkoxycarbonyl group, phenyl group or the same or different, halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group , C ₁ -C ₆ alkylsulfonyl group, halo
_{1 selected from} C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino group which may be the same or different, or C ₁ -C ₆ alkoxycarbonyl group
1 selected from substituted phenyl groups having the above substituents
A substituted C ₃ -C ₈ alkenylene group having the above substituents, C _3-
C ₈ alkynylene group or the same or different, halogen atom, cyano group, nitro group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C
_1- C ₆ alkylthio group, halo C _1- C ₆ alkylthio group, C _1-
C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, C ₁ -C ₆ alkylthio C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxycarbonyl group,

Phenyl group or may be the same or different and may be a halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C
₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group,
Halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C
₁ -C ₆ alkylamino group, which may be the same or different, di C _1-
A substituted C ₃ -C ₈ alkynylene group having one or more substituents selected from a substituted phenyl group having one or more substituents selected from a C ₆ alkylamino group or a C ₁ -C ₆ alkoxycarbonyl group is shown. Also, the above C ₁ -C ₈ alkylene group, substituted
C ₁ -C ₈ alkylene group, C ₃ -C ₈ alkenylene group, substituted C _3-
C ₈ alkenylene group, C ₃ -C ₈ alkynylene group or substituted C _3-
Any saturated carbon atom in the C ₈ alkynylene group may be substituted with a C ₂ -C ₅ alkylene group to represent a C ₃ -C ₆ cycloalkane ring, and the C ₁ -C ₈ alkylene group and the substituted C _1- Any two carbon atoms in the C ₈ alkylene group, C ₃ -C ₈ alkenylene group or substituted C ₃ -C ₈ alkenylene group together with the alkylene group or alkenylene group may form a C ₃ -C ₆ cycloalkane ring or It may also indicate a C ₃ -C ₆ cycloalkene ring.

R¹Is a hydrogen atom, mercapto group, C₁-C₆A
Rukiruthio group, halo C₁-C₆Alkylthio group, C₃-C₆Shiku
Lower alkyl group, halo C₃-C₆Cycloalkyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C ₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a phenylthio group, the same or
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
C₁-C₆ Alkylsulfonyl group, halo C₁-C₆Alkylsul
Honyl group, Mono C₁-C₆Alkylamino group,

C which may be the same or different₁-C₆Alkyl
Amino group or C₁-C₆Selected from alkoxycarbonyl groups
A substituted phenylthio group having one or more substituents,
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C ₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted heterocyclic group having a substituent or -A²-R^Four(In the formula, A² 
Is -C (= O)-, -C (= S)-, -C (= NR^Five)
-(In the formula, R^FiveIs a hydrogen atom, C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, Mono C₁-C₆Alkylamino group, same or
It may be different C₁-C₆Alkylamino group, C₁-C₆Al
Coxycarbonyl group, phenyl group or the same or different
May be, halogen atom, cyano group, nitro group,

C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C
_1- C ₆ alkylthio group, halo C _1- C ₆ alkylthio group, C _1-
C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, the same or different Good di C ₁ -C ₆ alkylamino group or C
A substituted phenyl group having one or more substituents selected from a _1- C ₆ alkoxycarbonyl group is shown. ), C ₁ -C ₈ alkylene group, halo C ₁ -C ₈ alkylene group, C ₃ -C ₆ alkenylene group, halo C ₃ -C ₆ alkenylene group, C ₃ -C ₆ alkynylene group or halo C ₃ -C ₆ Represents an alkynylene group,

(1) A² Is -C (= O)-, -C (=
S)-or -C (= NR^Five)-(Wherein R^FiveIs the same as above
Same. ) Indicates R^FourIs a hydrogen atom, C₁-C₆Alkyl
Group, halo c ₁-C₆Alkyl group, C₃-C₆Cycloalkyl group,
Halo c₃-C₆Cycloalkyl group, phenyl group, same or different
Can be halogen atom, cyano group, nitro group, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arco
Xy, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Phenyl group, heterocyclic group, which may be the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆An alkylsulfinyl group,

Halo C ₁ -C ₆ alkylsulfinyl group, C _1-
C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino group which may be the same or different, or C ₁ -C ₆ alkoxycarbonyl group A substituted heterocyclic group having one or more substituents selected from —Z ¹ —R ⁶ (wherein Z ¹ is —O—S
- or -N (R ⁷⁾ - (wherein, R ⁷ is a hydrogen atom, C ₁ -C ₆
Alkyl group, C ₁ -C ₆ Alkylcarbonyl group, halo C ₁ -C ₆
An alkylcarbonyl group or a C ₁ -C ₆ alkoxycarbonyl group is shown. R ⁶ is a hydrogen atom, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₃ -C ₆ alkenyl group, halo
C ₃ -C ₆ alkenyl group, C ₃ -C ₆ alkynyl group, halo C ₃ -C ₆
Alkynyl group, C ₃ -C ₆ cycloalkyl group, phenyl group,
May be the same or different, halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C
_1- C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group Group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino group which may be the same or different, or C _1- A substituted phenyl group having one or more substituents selected from C ₆ alkoxycarbonyl groups, a phenyl C ₁ -C ₄ alkyl group,

Halogen atoms, which may be the same or different,
Cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C ₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C ₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkylami
Group, which may be the same or different, di C₁-C₆Alkylamino
Group or C₁-C₆1 selected from alkoxycarbonyl groups
Substituted phenyl C having the above substituents on the ring₁-C_FourArchi
Group, heterocyclic group or the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Is a substituted heterocyclic group having one or more substituents. )
Indicates.

(2) A² Is C₁-C₈Alkylene group, halo C
₁-C₈Alkylene group, C₃-C₆Alkenylene group, halo C₃-C₆
Alkenylene group, C₃-C₆Alkynylene group or halo C₃-C₆
When an alkynylene group is shown, R^FourIs hydrogen atom, halogen
Atom, cyano group, nitro group, C ₃-C₆Cycloalkyl group,
Halo c₃-C₆Cycloalkyl group, C₁-C₆Alkoxy carbo
Nyl group, Mono C₁-C₆Alkylaminocarbonyl group, same
Or it may be different C ₁-C₆Alkylaminocarbonyl
Groups, phenyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C ₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
A substituted phenyl group having one or more substituents, a heterocyclic group,
May be one or different, a halogen atom, a cyano group,

Nitro group, C₁-C₆Alkyl group, halo C₁-C₆
Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arcoki
Shi group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C ₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkylami
Group, which may be the same or different, di C₁-C₆Alkylamino
Group or C₁-C₆1 selected from alkoxycarbonyl groups
Substituted heterocyclic group having the above substituents or -Z²-R ⁸(formula
Medium, Z² Is -O-, -S- -SO- -SO₂-, -N
(R⁹)-(Wherein R⁹Is a hydrogen atom, C₁-C₆Alkyl
Base, C₁-C₆Alkylcarbonyl group, halo C₁-C₆Alkyl
Carbonyl group, C₁-C₆Alkoxycarbonyl group, phenyl
Carbonyl group or may be the same or different and is halo.
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆An alkylsulfinyl group,

C ₁ -C ₆ alkylsulfonyl group or halo C ₁ -C
₆ shows a substituted phenylcarbonyl group having one or more substituents selected from an alkylsulfonyl group. ), -C
(= O) - or -C (= NOR ¹⁰⁾ - (wherein, R ¹⁰ is a hydrogen atom, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₃
-C ₆ alkenyl group, halo C ₃ -C ₆ alkenyl group, C ₃ -C ₆ alkynyl group, halo C ₃ -C ₆ alkynyl group, C ₃ -C ₆ cycloalkyl group, phenyl C ₁ -C ₄ alkyl group or May be the same or different, a halogen atom, a cyano group, a nitro group,
C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group , C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C _1-
C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino group which may be the same or different, or C ₁ -C ₆ alkoxycarbonyl group Represents a substituted phenyl C ₁ -C ₄ alkyl group having on the ring one or more substituents selected from ),
R ⁸ is a hydrogen atom, a C ₁ -C ₆ alkyl group,

Halo C₁-C₆Alkyl group, C₃-C₆Alkenyl
Group, halo c₃-C₆Alkenyl group, C₃-C₆Alkynyl group, ha
B C₃-C₆Alkynyl group, C₃-C₆Cycloalkyl group, C₁-
C₆Alkylcarbonyl group, halo C₁-C₆Alkyl Carboni
Ru radical, C₁-C₆Alkoxycarbonyl group, Mono C₁-C₆Al
Killaminocarbonyl group, which may be the same or different, di C
₁-C₆Alkylaminocarbonyl group, phenyl group, same or
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C ₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group, halo C₁-C₆Alkylsul
Honyl group, Mono C₁-C₆Alkylamino group, same or different
I'm good C₁-C₆Alkylamino group or C₁-C₆Arco
Having one or more substituents selected from oxycarbonyl groups
Substituted phenyl group, phenyl C₁-C_FourAlkyl group, same or
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group,

Halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, Substituted phenyl having on the ring one or more substituents selected from mono C ₁ -C ₆ alkylamino groups, di C ₁ -C ₆ alkylamino groups which may be the same or different, or C ₁ -C ₆ alkoxycarbonyl groups C ₁ -C ₄ alkyl group, heterocyclic group or may be the same or different, halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ Alkoxy group, halo C ₁ -C ₆ alkoxy group,
C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C
_1- C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆
Alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group,
Di C ₁ -C ₆ alkylamino groups which may be the same or different or
A substituted heterocyclic group having one or more substituents selected from C ₁ -C ₆ alkoxycarbonyl groups is shown. ) Is shown. ) Is shown. R ¹ may combine with A ¹ to form a 5- to 8-membered ring which may be interrupted by 1 or 2 identical or different oxygen atoms, sulfur atoms or nitrogen atoms.

R ² and R ³ may be the same or different,
Hydrogen atom, C ₃ -C ₆ cycloalkyl group or -A ² -R ⁴ (wherein, A ² and R ⁴ are the same. Above) shows a. R ² may combine with A ¹ or R ¹ to form a 5 to 7 membered ring which may be interrupted by ¹ or 2 identical or different oxygen, sulfur or nitrogen atoms. it can. X's may be the same or different and are a halogen atom, a cyano group, a nitro group, a C ₃ -C ₆ cycloalkyl group, a halo C ₃ -C ₆ cycloalkyl group, a C ₁ -C ₆ alkoxycarbonyl group, a phenyl group, the same. Or they may be different, a halogen atom, a cyano group, a nitro group, a C ₁ -C ₆ alkyl group, a halo C ₁ -C ₆ alkyl group, C ₁ -C
₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C _1- C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group,

C which may be the same or different₁-C₆Alkyl
Amino group or C₁-C₆Selected from alkoxycarbonyl groups
A substituted phenyl group having one or more substituents, a heterocycle
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C ₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted heterocyclic group having a substituent or -A³-R¹¹(In the formula, A³ 
Is -O-, -S-, -SO-, -SO₂-, -C (=
O)-, -C (= NOR¹²)-(Wherein R¹²Is hydrogen
Child, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₃-C₆
Alkenyl group, halo C₃-C₆Alkenyl group, C₃-C₆Archi
A nyl group,

C ₃ -C ₆ cycloalkyl group, phenyl C ₁ -C ₄
Alkyl groups, which may be the same or different, are a halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C
₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, Halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group,
One or more selected from halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino group which may be the same or different, or C ₁ -C ₆ alkoxycarbonyl group Represents a substituted phenyl C ₁ -C ₄ alkyl group having the substituent of ₁ on the ring. ), C ₁ -C ₆ alkylene groups, halo C ₁ -C ₆
An alkylene group, C ₂ -C ₆ alkenylene group, halo C ₂ -C ₆ alkenylene group, C ₂ -C ₆ alkynylene group or halo C ₃ -C ₆ alkynylene group,

(1) A³Is -O-, -S-, -SO- or
Is -SO₂-Indicates R¹¹Is halo c₃-C₆Cycloal
Kill group, halo C₃-C₆Cycloalkenyl group, phenyl group,
They may be the same or different and may be a halogen atom, a cyano group, or
Toro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆A
Rukiruthio group, halo C₁-C₆Alkylthio group, C₁-C₆Al
Kirsulfinyl group, halo C₁-C₆Alkylsulfinyl
Base, C₁-C₆Alkylsulfonyl group, halo C₁-C₆Alkyl
Sulfonyl group, mono C₁-C₆Alkylamino group, same or
It may be different C₁-C₆Alkylamino group or C₁-C₆A
One or more substituents selected from lucoxycarbonyl groups
Having a substituted phenyl group, a heterocyclic group, the same or different
Well, halogen atom, cyano group, nitro group, C₁-C₆Al
Kill group, halo C₁-C₆Alkyl group, C ₁-C₆An alkoxy group,
Halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,

Halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, A mono-C ₁ -C ₆ alkylamino group, a di-C ₁ -C ₆ alkylamino group which may be the same or different, or a substituted heterocyclic group having one or more substituents selected from a C ₁ -C ₆ alkoxycarbonyl group, or -A ⁴ -R ¹³ (wherein A ⁴ is C _1-
A C ₆ alkylene group, a halo C ₁ -C ₆ alkylene group, a C ₃ -C ₆ alkenylene group, a halo C ₃ -C ₆ alkenylene group, a C ₃ -C ₆ alkynylene group or a halo C ₃ -C ₆ alkynylene group, R ¹³ may be a hydrogen atom, a halogen atom, a C ₃ -C ₆ cycloalkyl group, a halo C ₃ -C ₆ cycloalkyl group, a C ₁ -C ₆ alkoxycarbonyl group, a phenyl group, the same or different, a halogen atom, Cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C
_1- C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group,

Halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, A mono C ₁ -C ₆ alkylamino group, a diphenyl C ₁ -C ₆ alkylamino group which may be the same or different, or a substituted phenyl group having one or more substituents selected from a C ₁ -C ₆ alkoxycarbonyl group; A ⁵ -R ¹⁴ (wherein, A ⁵ is -
O -, - S -, - SO -, - SO 2 - or -C (= O)
- are shown, R ¹⁴ is C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₃ -C ₆ alkenyl group, halo C ₃ -C ₆ alkenyl group,
C ₃ -C ₆ alkynyl group, halo C ₃ -C ₆ alkynyl group, C ₃ -C ₆
Cycloalkyl group, halo C ₃ -C ₆ cycloalkyl group, phenyl group, may be the same or different, halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group,
C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C
₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group,

C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆
Alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group,
Di C ₁ -C ₆ alkylamino groups which may be the same or different or
A substituted phenyl group having one or more substituents selected from C ₁ -C ₆ alkoxycarbonyl groups, a heterocyclic group, which may be the same or different, a halogen atom, a cyano group, a nitro group, a C ₁ -C ₆ alkyl group , Halo C ₁ -C ₆ alkyl group, C ₁ -C ₆
Alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group,
C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino group which may be the same or different, or C ₁ -C ₆ A substituted heterocyclic group having one or more substituents selected from an alkoxycarbonyl group is shown. ),

(2) A³ Is -C (= O)-or -C (=
NOR¹²)-(Wherein R¹²Is the same as above. )
If R¹¹Is a hydrogen atom, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₂-C₆Alkenyl group, halo C₂-C₆Alkenyl
Base, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalk
Ru radical, C₁-C₆Alkoxy group, C₁-C₆Alkylthio group,
No C₁-C₆An alkylamino group, which may be the same or different
C₁-C₆Alkylamino group, phenyl group, same or different
May be, halogen atom, cyano group, nitro group, C ₁-C₆
Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆Al
Killsulfonyl group, halo C₁-C₆An alkylsulfonyl group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group or C₁-C₆Alkoxy carbo
Substituted Fe having one or more substituents selected from the group
Nyl group, phenylamino group, may be the same or different,
Halogen atom, cyano group, nitro group,

C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C
_1- C ₆ alkylthio group, halo C _1- C ₆ alkylthio group, C _1-
C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, the same or different Good di C ₁ -C ₆ alkylamino group or C
A substituted phenylamino group having on its ring one or more substituents selected from ₁ -C ₆ alkoxycarbonyl groups, a heterocyclic group or the same or different, a halogen atom, a cyano group, a nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C
_1- C ₆ alkylthio group, halo C _1- C ₆ alkylthio group, C _1-
C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, the same or different Good di C ₁ -C ₆ alkylamino group or C
A substituted heterocyclic group having one or more substituents selected from a _1- C ₆ alkoxycarbonyl group,

(3) A ³ is a C ₁ -C ₆ alkylene group, halo C
₁ -C ₆ alkylene group, C ₂ -C ₆ alkenylene group, halo C ₂ -C ₆
Alkenylene group, C ₂ -C ₆ alkynylene group or halo C ₃ -C ₆
When representing an alkynylene group, R ¹¹ is hydrogen atom, hydroxy group, halogen atom, C ₃ -C ₆ cycloalkyl group, halo C
_3- C ₆ cycloalkyl group, C ₁ -C ₆ alkoxycarbonyl group, phenyl group, which may be the same or different, halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C
₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino which may be the same or different Group or a substituted phenyl group having one or more substituents selected from C ₁ -C ₆ alkoxycarbonyl groups, a heterocyclic group, which may be the same or different, a halogen atom, a cyano group, a nitro group, C ₁ -C ₆ Alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C
₆ alkoxy group, halo C ₁ -C ₆ alkoxy group,

C₁-C₆Alkylthio group, halo C₁-C₆Archi
Ruthio group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆
Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Substituted heterocyclic group having one or more substituents or -A⁶-
R¹⁵(In the formula, A⁶ Is -O-, -S-, -SO- or -S
O₂-Indicates R¹⁵Is C₃-C₆Cycloalkyl group, halo C
₃-C₆Cycloalkyl group, phenyl group, the same or different
Also good, halogen atom, cyano group, nitro group, C₁-C₆A
Rukiru group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆Al
Killsulfonyl group, halo C₁-C₆An alkylsulfonyl group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group or C ₁-C₆Alkoxy carbo
Substituted Fe having one or more substituents selected from the group
Nyl group, heterocyclic group, which may be the same or different, halogen
Atom, cyano group,

Nitro group, C₁-C₆Alkyl group, halo C₁-C₆
Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arcoki
Shi group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C ₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkylami
Group, which may be the same or different, di C₁-C₆Alkylamino
Group or C₁-C₆1 selected from alkoxycarbonyl groups
Substituted heterocyclic group having the above substituents or -A⁷-R ¹⁶(formula
Medium, A⁷ Is C₁-C₆Alkylene group, halo C₁-C₆Alkylene
Base, C₂-C₆Alkenylene group, halo C₂-C₆Alkenylene
Base, C₂-C₆Alkynylene group or halo C₃-C₆Alkynylene
Group, R¹⁶Is hydrogen atom, halogen atom, C₃-C₆Shiku
Lower alkyl group, halo C₃-C₆Cycloalkyl group, C₁-C₆A
Lucoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkyl
Thio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyls
Rufinyl group, halo C₁-C₆Alkylsulfinyl group, C
₁-C₆Alkylsulfonyl group, halo C₁-C₆Alkyl sulfo
Nyl group, phenyl group, may be the same or different,

Halogen atom, cyano group, nitro group, C _1-
C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆
Selected from alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkylamino group which may be the same or different, or C ₁ -C ₆ alkoxycarbonyl group A substituted phenyl group having one or more substituents, a phenoxy group, which may be the same or different,
Halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo
C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C _1-
C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C _1-
C ₆ alkylamino group, which may be the same or different, C ₁ -C ₆
A substituted phenoxy group having one or more substituents selected from an alkylamino group or a C ₁ -C ₆ alkoxycarbonyl group, a phenylthio group, which may be the same or different, a halogen atom, a cyano group,

Nitro group, C₁-C₆Alkyl group, halo C₁-C₆
Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arcoki
Shi group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C ₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkylami
Group, which may be the same or different, di C₁-C₆Alkylamino
Group or C₁-C₆1 selected from alkoxycarbonyl groups
Substituted phenylthio group, heterocyclic group or the above having the above substituents
May be the same or different, and may be a halogen atom, cyano
Group, nitro group, C ₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A heterocyclic group having a substituent is shown. ) Is shown. ), L
Represents an integer of 0 to 4.

X can form a condensed ring together with adjacent carbon atoms on the phenyl ring, and the condensed rings may be the same or different, and a halogen atom, a cyano group, a nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁
-C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C
₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, may be the same or different Di C ₁ -C ₆ alkylamino group or C
It can also have one or more substituents selected from ₁ -C ₆ alkoxycarbonyl groups.

Y may be the same or different and may be a halogen atom, a cyano group, a nitro group, a halo C ₃ -C ₆ cycloalkyl group, the same or different tri C ₁ -C ₆ alkylsilyl group, a phenyl group, May be the same or different, and may be a halogen atom, a cyano group, a nitro group, a C ₁ -C ₆ alkyl group, a halo C _1-
C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C _1- C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, mono C ₁ -C ₆ alkylamino group, di C ₁ -C ₆ alkyl which may be the same or different A substituted phenyl group having one or more substituents selected from an amino group or a C ₁ -C ₆ alkoxycarbonyl group, a heterocyclic group, which may be the same or different, a halogen atom, a cyano group, a nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C _1-
C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, A C ₁ -C ₆ alkylsulfonyl group,

Halo C ₁ -C ₆ alkylsulfonyl group, mono C
₁ -C ₆ alkylamino group, which may be the same or different, di C _1-
C ₆ alkylamino group or a C ₁ -C ₆ alkoxy substituted heterocyclic group, or -A ³ -R ¹¹ have one or more substituents selected from the group (wherein, A ³ and R ¹¹ are as defined above. ) Is shown and m shows the integer of 0-5. Y may combine with adjacent carbon atoms on the phenyl ring to form a condensed ring, which may be the same or different, and may be a halogen atom, a C ₁ -C ₆ alkyl group, a halo group. C ₁ -C ₆ alkyl group,
C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆
Alkylthio group, halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group, Phenyl group, which may be the same or different, halogen atom, cyano group, nitro group, C ₁ -C ₆ alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ Alkoxy group, C ₁ -C ₆ alkylthio group, halo C
₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group,
Halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group,

Substituted phenyl having one or more substituents selected from mono C ₁ -C ₆ alkylamino groups, di C ₁ -C ₆ alkylamino groups which may be the same or different, or C ₁ -C ₆ alkoxycarbonyl groups Groups, heterocyclic groups or the same or different, halogen atom, cyano group, nitro group, C ₁ -C ₆
Alkyl group, halo C ₁ -C ₆ alkyl group, C ₁ -C ₆ alkoxy group, halo C ₁ -C ₆ alkoxy group, C ₁ -C ₆ alkylthio group,
Halo C ₁ -C ₆ alkylthio group, C ₁ -C ₆ alkylsulfinyl group, halo C ₁ -C ₆ alkylsulfinyl group, C ₁ -C ₆ alkylsulfonyl group, halo C ₁ -C ₆ alkylsulfonyl group,
Mono C ₁ -C ₆ alkylamino group, substituted heterocyclic group having one or more substituents selected from the same or different and may di C ₁ -C ₆ alkylamino group or a C ₁ -C ₆ alkoxycarbonyl group It can also have one or more substituents selected. n shows the integer of 0-2.

However, when X, R ² and R ³ simultaneously represent a hydrogen atom, m represents an integer of 2, Y represents a fluorine atom in the 2-position and chlorine atom in the 3-position, A ¹ represents propylene. And R ¹ is a methyl group and n is an integer of 0. Moreover, the general formula (I) phthalamide derivative represented by the N ² - (1,1-dimethyl-2-methylthioethyl) -3-iodo -N ¹ - {2-methyl-4- [1,
2,2,2-Tetrafluoro-1- (trifluoromethyl) ethyl] phenyl} phthalamide, N ^2- (1,1
- dimethyl-2-methylsulfonyl-ethyl) -3-iodo -N ¹ - {2-methyl-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl} phthalamide or N ^2- (1,1-dimethyl-2
- methylsulfinyl-ethyl) -3-iodo -N ¹ -
Except when it is {2-methyl-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl} phthalamide. The present invention relates to an agricultural and horticultural insecticide containing as an active ingredient a phthalamide derivative represented by the general formula (I) or a salt thereof containing a phthalamide derivative or a salt thereof and a known compound.

[0038]

BEST MODE FOR CARRYING OUT THE INVENTION In the definition of the general formula (I) of the phthalamide derivative or salt thereof of the present invention, the "halogen atom" means a chlorine atom, a bromine atom, an iodine atom or a fluorine atom, and "C ₁ -C ₆ "Alkyl" means, for example, methyl, ethyl,
A linear or branched alkyl group having 1 to 6 carbon atoms such as n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, n-pentyl, n-hexyl. And "halo C ₁ -C ₆ alkyl" represents a linear or branched alkyl group having 1 to 6 carbon atoms, which is substituted with one or more halogen atoms which may be the same or different, “C ₁ -C ₈ alkylene” means a linear or branched alkylene group having 1 to 8 carbon atoms such as methylene, ethylene, propylene, trimethylene, dimethylmethylene, tetramethylene, isobutylene, dimethylethylene, octamethylene and the like. Show. Also, "R ¹ and R ² are bound to each other by 1
˜3 to 4 same or different oxygen atom, sulfur atom or nitrogen atom which may be interrupted by 4 to 7 membered ring ”are, for example, perhydrothiazine ring, thiazolidine ring, thiazetidine ring and dihydrothiazine ring. , A thiazoline ring, a perhydrooxathiazine ring, a dihydrooxathiazine ring, a dithiazine ring, a perhydrodithiazine ring, and the like.

The "heterocyclic group" is a 5- or 6-membered heterocyclic group having one or more heteroatoms selected from oxygen atom, sulfur atom or nitrogen atom, and examples thereof include pyridyl group and pyridine-N-oxide group. , Pyrimidinyl group, furyl group,
Tetrahydrofuryl group, thienyl group, tetrahydrothienyl group, tetrahydropyranyl group, tetrahydrothiopyranyl group, oxazolyl group, isoxazolyl group, oxadiazolyl group, thiazolyl group, isothiazolyl group, thiadiazolyl group, imidazolyl group, trithiazolyl group, pyrazolyl group, etc. Examples of the “fused ring” include naphthalene, tetrahydronaphthalene, indene, indane, quinoline, quinazoline, indole,
Examples thereof include indoline, chroman, isochroman, benzodioxane, benzodioxole, benzofuran, dihydrobenzofuran, benzothiophene, dihydrobenzothiophene, benzoxazole, benzothiazole, benzimidazole and indazole.

Examples of the salt of the phthalamide derivative represented by the general formula (I) of the present invention include inorganic acid salts such as hydrochloride, sulfate, nitrate and phosphate, acetate, fumarate, maleate, Examples thereof include organic acid salts such as oxalate, methanesulfonate, benzenesulfonate, and paratoluenesulfonate, and salts with sodium ion, potassium ion, calcium ion and the like. The phthalamide derivative represented by the general formula (I) of the present invention may contain an asymmetric carbon atom or an asymmetric center in its structural formula, and may have two optical isomers. Includes all optical isomers and mixtures containing them in arbitrary proportions. The phthalamide derivative represented by the general formula (I) of the present invention can be produced, for example, by the production method illustrated below.

Manufacturing Method 1.

[Chemical 4] (In the formula, R ¹ , R ² , A ¹ , X, Y, 1, m and n are the same as above.)

By reacting the phthalic anhydride derivative represented by the general formula (V) with the aniline represented by the general formula (IV) in the presence of an inert solvent, the phthalic anhydride derivative represented by the general formula (III) can be obtained. And a phthalimide derivative (I
By reacting II) with or without isolation and reacting with an amine represented by the general formula (II), a phthalamide derivative represented by the general formula (I-1) can be produced. (1). General formula (V) → general formula (III) The inert solvent that can be used in this reaction may be any one that does not significantly inhibit the progress of this reaction, for example, aromatic hydrocarbons such as benzene, toluene and xylene, Halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, chlorinated aromatic hydrocarbons such as chlorobenzene and dichlorobenzene, chain or cyclic ethers such as diethyl ether, dioxane and tetrahydrofuran, esters such as ethyl acetate , Dimethylformamide, amides such as dimethylacetamide, acids such as acetic acid, dimethylsulfoxide, inert solvents such as 1,3-dimethyl-2-imidazolidinone can be exemplified, and these inert solvents are independent. It is possible to use two or more kinds in combination.

Since this reaction is an equimolar reaction, it is sufficient to use each reactant in an equimolar amount, but it is also possible to use any one of the reactants in excess. This reaction can be carried out under dehydration conditions, if necessary. The reaction temperature may be room temperature to the reflux temperature of the inert solvent used, and the reaction time may vary depending on the reaction scale, reaction temperature, etc., but may be appropriately selected within the range of several minutes to 48 hours. After the reaction,
It may be isolated from the reaction system containing the desired product by a conventional method,
If necessary, the desired product can be produced by purification by recrystallization, column chromatography, or the like. or,
It is also possible to use for the next reaction step without isolating the desired product from the reaction system. The phthalic anhydride derivative represented by the general formula (V) is described in J. Org. Chem. , 52 , 129 (198
7), J. Am. Chem. Soc. , 51 , 1865
(1929), ibid., 63 , 1542 (1941) and the like. The anilines represented by the general formula (IV) can be produced by the method described in J. Org. Chem. , 29 , 1
(1964), Angew. Chem. Int. Ed.
Engl. , 24 , 871 (1985), Synthe.
sis, 1984 , 667, Journal of the Chemical Society of Japan, 1973 ,
2351, DE-2606982, JP 1-9
It can be manufactured by the method described in JP-A No. 0163.

(2). General formula (III) → General formula (I-1) As the inert solvent which can be used in this reaction, the inert solvent which can be used in (1) can be exemplified. Since this reaction is an equimolar reaction, each reaction agent may be used in an equimolar amount, but the amines represented by the general formula (II) may be used in excess. The reaction temperature may be room temperature to the reflux temperature of the inert solvent used, and the reaction time may vary depending on the reaction scale, reaction temperature, etc., but may be appropriately selected within the range of several minutes to 48 hours. After completion of the reaction, it may be isolated from the reaction system containing the desired product by a conventional method, and if necessary, the desired product can be produced by purification by recrystallization, column chromatography or the like.

Manufacturing method 2.

[Chemical 5]

[0046]

[Chemical 6] (In the formula, R ¹ , R ² , A ¹ , X, Y, 1, m and n are the same as defined above, and X ′ represents a halogen atom or a nitro group, provided that X is a hydrogen atom or a nitro group. .)

By reacting the phthalimide derivative represented by the general formula (III-1) with a reactant corresponding to X in the presence of an inert solvent, the phthalic acid derivative represented by the general formula (III) As an imide derivative, the phthalamide derivative represented by the general formula (I-1) is obtained by reacting the phthalimide derivative (III) with or without isolation and reacting with the amine represented by the general formula (II). Can be manufactured. (1) General formula (III-1) → general formula (III) Org. Chem. , 42 , 3415 (1
977), Tetrahedron, 25 , 5921.
(1969), Synthesis, 1984 , 66.
7, Chem. Lett. , 1973 , 471, J. Am. O
rg. Chem. , 39 , 3318 (1974), ibid. 3
9 , 3327 (1974) and the like. (2). General formula (III) → General formula (I-1) This reaction can be manufactured according to the manufacturing method 1- (2).

Manufacturing method 3.

[Chemical 7]

[0049]

[Chemical 8] (In the formula, R ¹ , R ² , R ³ , A ¹ , X, Y, 1, m and n are the same as above.)

Phthalic anhydride derivative represented by the general formula (V)
And an amine represented by the general formula (II) in the presence of an inert solvent.
By reacting below, it is represented by the general formula (III-4)
Phthalamic acids, and the phthalamic acids (III-4)
R with or without isolation ²Phthalate is a hydrogen atom
In the case of amic acids (III-4), condensation reaction in the presence of a condensing agent
To give a compound represented by the general formula (VI):
I) may or may not be isolated in the presence of an inert solvent.
Reaction with anilines of general formula (IV ')
R of amide acids (III-4)²Is a hydrogen atom other than hydrogen atom
In the case of amide acids (III-4), the anilines represented by the general formula (IV)
The condensation reaction in the presence of
It is possible to produce a phthalamide derivative represented by the formula (I).
Wear.

Alternatively, by reacting the phthalic anhydride derivative represented by the general formula (V) with the anilide represented by the general formula (IV ′) in the presence of an inert solvent, the general formula (III-5 ) And the phthalamic acids (I
II-5) is isolated or not isolated, and when R ³ is a phthalamic acid (III-5) in which R ³ represents a hydrogen atom, the condensation reaction is carried out in the presence of a condensing agent to give a compound represented by the general formula (VI-1) Represented as a compound,
The compound (VI-1) is isolated or not isolated and reacted with an amine represented by the general formula (II) in the presence of an inert solvent,
When R ³ is a phthalamic acid (III-5) other than a hydrogen atom, a phthalamide represented by the general formula (I) is obtained by subjecting the amines represented by the general formula (II) to a condensation reaction in the presence of a condensing agent. Derivatives can be prepared.

(1). General formula (V) or general formula (VI-1) → general formula (III-4) or general formula (I) This reaction may be carried out in the same manner as in production method 1- (2) to produce the desired product. it can. (2). General formula (III-4) or general formula (III-5) → general formula (V
I) or the general formula (VI-1). Med. Chem. , 10 , 982 (19
The target product can be produced according to the method described in 67). It can also be produced by reacting the phthalamic acid derivative represented by the general formula (III-4) or the general formula (III-5) in the presence of a condensing agent and an inert solvent. This reaction can be carried out in the presence of a base, if necessary.

Examples of the inert solvent used in this reaction include tetrahydrofuran, diethyl ether, methyl
Examples thereof include t-butyl ether, dioxane, chloroform, methylene chloride, chlorobenzene, toluene, acetonitrile, ethyl acetate and butyl acetate. The condensing agent used in this reaction may be any one commonly used in amide synthesis, and examples thereof include Mukaiyama reagent (2
-Chloro-N-methylpyridinium iodide),
DCC (1,3-dicyclohexylcarbodiimide),
Examples thereof include CDI (carbonyldiimidazole), methyl chloroformate, DEPC (diethyl cyanophosphate), and the amount thereof is represented by the general formula (III-4) or the general formula (III-5). It may be appropriately selected and used from the range of equimolar to excess molar to the phthalamic acid derivative.

Examples of the base that can be used in this reaction include organic bases such as triethylamine and pyridine, and inorganic bases such as potassium carbonate, sodium hydrogencarbonate, sodium carbonate and sodium hydroxide. May be appropriately selected and used from the equimolar to excess molar range relative to the phthalamic acid derivative represented by the general formula (III-4) or the general formula (III-5). The reaction temperature can be 0 ° C. to the boiling point of the inert solvent used, and the reaction time is not constant depending on the reaction scale, reaction temperature, etc., but is in the range of several minutes to 48 hours. After completion of the reaction, it may be isolated from the reaction system containing the desired product by a conventional method, and if necessary, the desired product can be produced by purification by recrystallization, column chromatography or the like. (3). General Formula (VI) or General Formula (V) → General Formula (I) or General Formula (III-5) This reaction can be carried out in the same manner as in Production Method 1- (2) to produce the desired product.

(4). General formula (III-4) or general formula (III-
5) → general formula (I) a phthalamic acid derivative represented by the general formula (III-4) or the general formula (III-5), and an amine represented by the general formula (II) or the general formula (IV ') Can be produced by reacting in the presence of a condensing agent and an inert solvent. This reaction can also be carried out in the presence of a base, if necessary. Examples of the inert solvent used in this reaction include tetrahydrofuran, diethyl ether, dioxane, chloroform, methylene chloride and the like. The condensing agent used in this reaction may be any one used in ordinary amide synthesis, such as Mukaiyama reagent (2-chloro-N-methylpyridinium iodide), DCC (1,3-dicyclohexylcarbodiimide), CDI. (Carbonyldiimidazole), DEPC (diethyl cyanophosphate) and the like can be exemplified, and the amount used is based on the phthalamic acid derivative represented by the general formula (III-4) or the general formula (III-5). It may be appropriately selected and used from the range of equimolar to excess molar.

Examples of the base that can be used in this reaction include organic bases such as triethylamine and pyridine, and inorganic bases such as potassium carbonate. The phthalamic acid derivative represented by the formula (III-5) may be appropriately selected and used from the equimolar to excess molar range. The reaction temperature can be 0 ° C. to the boiling point of the inert solvent used, and the reaction time is not constant depending on the reaction scale, reaction temperature, etc., but is in the range of several minutes to 48 hours. After completion of the reaction, it may be isolated from the reaction system containing the desired product by a conventional method, and if necessary, the desired product can be produced by purification by recrystallization, column chromatography or the like.

Manufacturing Method 4.

[Chemical 9]

[0058]

[Chemical 10] (In the formula, R ¹ , R ² , A ¹ , X, Y, 1, m and n are the same as the above, and Hal represents a halogen atom.)

[0059]

[Chemical 11] (In the formula, R ¹ , Y and m are the same as above.)

By reacting the benzoic acid halide represented by the general formula (VII) with the amine derivative represented by the general formula (II) or (IV ') in the presence of an inert solvent, the general formula
A benzamide represented by (VII-1) or (VII-2),
The benzamide, for example, after orthometallation using a metal reagent such as butyllithium, directly reacted with the isocyanate represented by the general formula (IX-1) or (IV-2),
Or reacted with carbon dioxide, the general formula (III-4 ') or (III-
After producing phthalamic acid represented by 5 '), production method 3
-By performing the same as (1) to (4), the general formula (I)
The phthalamide derivative represented by can be produced. (1). General formula (VII) → general formula (VIII-1) or general formula (VII
I-2) This reaction is based on J. Org. Chem. 32 , 3069 (19
The target product can be produced by the method described in 67) or the like.

(2). General formula (VIII-1) or general formula (VIII-
2) → general formula (I) In this reaction, benzamides represented by the general formula (VIII-1) or general formula (VIII-2) can be prepared according to J. Org. Chem. 29 , 85
3 (1964), followed by ortholithiation, followed by reaction with an isocyanate represented by the general formula (IX-1) or (IX-2) at −80 ° C. to room temperature. it can. (3). General formula (VIII-1) or general formula (VIII-2) → general formula (I
II-4 ′) or general formula (III-5 ′) This reaction is carried out by ortholithiation in the same manner as in (2), and then introducing carbon dioxide at −80 ° C. to room temperature.
The target product can be manufactured. After completion of the reaction, it may be isolated from the reaction system containing the desired product by a conventional method, and if necessary, the desired product can be produced by purification by recrystallization, column chromatography or the like. (4). General formula (III-4 ') or general formula (III-5') → general formula
(I) This reaction can be carried out in the same manner as in Production Method 3- (1) to (4) to produce the desired product.

Manufacturing Method 5.

[Chemical 12] (In the formula, R ¹ , R ² , R ³ , A ¹ , X, Y, l, m and n are the same as described above, provided that n is not an integer of 0.)

The phthalamide derivative represented by the general formula (I-3) can be produced by reacting the phthalamide derivative represented by the general formula (I-2) with an oxidizing agent in the presence of an inert solvent. it can. Examples of the inert solvent used in this reaction include halogenated hydrocarbons such as methylene chloride and chloroform, aromatic hydrocarbons such as toluene and xylene, acids such as acetic acid, and alcohols such as methanol, ethanol and propanol. It can be illustrated. Examples of the oxidizing agent include metachloroperbenzoic acid, peracetic acid, potassium metaperiodate, potassium hydrogen persulfate (oxone), hydrogen peroxide, and the like, and the amount thereof is represented by the general formula (I-2). It may be used by appropriately selecting from the range of 0.5 to 3 equivalents with respect to the phthalamide derivative represented by. The reaction temperature may be in the range of −50 ° C. to the boiling point range of the inert solvent used, and the reaction time is not constant depending on the reaction temperature, reaction scale, etc., but is in the range of several minutes to 24 hours.
After completion of the reaction, it may be isolated from the reaction system containing the desired product by a conventional method, and if necessary, the desired product can be produced by purification by recrystallization, column chromatography or the like.

Representative compounds of the phthalamide derivative represented by the general formula (I) are shown below in Table 1, Table 2 and Table 3, but the present invention is not limited thereto. General formula (I)

[Chemical 13]

[0065]

[0066]

[0067]

[0068]

[0069]

[0070]

[0071]

[0072]

[0073]

[0074]

[0075]

[0076]

[0077]

[0078]

[0079]

[0080]

[0081]

[0082]

[0083]

[0084]

[0085]

[0086]

[0087]

[0088]

[0089]

[0090]

[0091]

[0092]

[0093]

[0094]

[0095]

[0096]

[0097]

[0098]

[0099]

General formula (I)

[Chemical 14]

[0101] In Tables 1 to 3, “Ph” means a phenyl group and “Py”
“I” is a pyridyl group, “Pym” is a pyrimidyl group,
"Thz" is a thiazolyl group, "Thd" is a thiadiazolyl group, "Bzt" is a benzothiazolyl group, and "c-" is an alicyclic hydrocarbon group, and Q ^{1 to} Q ¹⁶ are compounds shown below. Show.

[0102]

[Chemical 15]

In Tables 1 to 3, ¹ H-NMR data of the compounds whose physical properties are paste are shown in Table 4.

Typical examples of the present invention will be illustrated below, but the present invention is not limited thereto.

EXAMPLES Example 1. (1-1). N- [4- (1,1,2,3,3,3-hexafluoropropoxy) -1-methylphenyl] -3
-Production of nitrophthalimide. 3-nitrophthalic anhydride 1.93 g and 4- (1,1,
2.73 g of 2,3,3,3-hexafluoropropoxy) -1-methylaniline was dissolved in 30 ml of acetic acid, and the reaction was carried out under heating under reflux for 3 hours. After completion of the reaction, the solvent was distilled off under reduced pressure, and the obtained residue was washed with an ether-hexane mixed solvent to obtain 4.4 g of the desired product. Physical property: m. p. 121 ℃ Yield: 98%

(1-2). N ^1- [4- (1,1,2,
3,3,3-hexafluoro-propoxy) -1-methylphenyl] -N ² - (1-methyl-2-methylthioethyl) -3-Nitorofutaramido (Compound No. 223). 0.54 g of N- [4- (1,1,2,3,3,3-hexafluoropropoxy) -1-methylphenyl] -3-nitrophthalimide was dissolved in 10 ml of dioxane, and 1-methyl- was added to the solution. 2-methylthioethylamine 0.2
5 g and 0.01 g of acetic acid were added, and the reaction was carried out under heating under reflux for 3 hours. After completion of the reaction, the solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography using a mixed solvent of hexane / ethyl acetate = 1/1 as an eluent to give an Rf value of 0.4 to 0. .5 target 0.4
5 g was obtained. Physical property: m. p. 218 ° C Yield: 68%

Example 2. (2-1). Preparation of 3-fluoro-N- (4-heptafluoroisopropyl-2-methylphenyl) phthalimide. 1.33 g of 3-fluorophthalic anhydride and 4-heptafluoroisopropyl-2-methylaniline were added to 10 m of acetic acid.
It was dissolved in 1 and reacted for 3 hours under reflux. After completion of the reaction, the solvent was distilled off under reduced pressure, and the obtained residue was washed with an ether-hexane mixed solvent to obtain the desired product 3.
1 g was obtained. Physical property: m. p. 155-157 ° C Yield: 97% (2-2). N- (4-heptafluoroisopropyl-
Preparation of 2-methylphenyl) -3-methylthiophthalimide. 2.54 g of 3-fluoro-N- (4-heptafluoroisopropyl-2-methylphenyl) phthalimide was dissolved in 20 ml of dimethylformamide, 2.8 g of a 15% aqueous solution of methyl mercaptan was added to the solution, and the mixture was stirred at room temperature for 3 hours. Was reacted. After the reaction was completed, the reaction solution was poured into water, the desired product was extracted with ethyl acetate, the extract was dried over anhydrous magnesium, the solvent was distilled off under reduced pressure, and the resulting residue was mixed with ether-hexane. By washing, 2.2 g of the target product was obtained. Physical property: m. p. 163-165 ° C Yield: 81%

(2-3). Preparation of N- (4-heptafluoroisopropyl-2-methylphenyl) -3-methylsulfonylphthalimide. 0.63 g of N- (4-heptafluoroisopropyl-2-methylphenyl) -3-methylthiophthalimide was dissolved in 20 ml of methylene chloride, 0.58 g of metachloroperbenzoic acid was added to the solution under ice cooling, and the mixture was allowed to stand at room temperature. The reaction was carried out. After completion of the reaction, the reaction solution was poured into water, the desired product was extracted with chloroform, the organic layer was washed with an aqueous sodium thiosulfate solution and an aqueous potassium carbonate solution, dried over anhydrous magnesium, and the solvent was distilled off under reduced pressure. The obtained residue was washed with an ether-hexane mixed solvent to obtain 0.63 g of the desired product. Physical property: m. p. 185-187 ° C Yield: 93%

(2-4). N ¹ - (4-heptafluoroisopropyl-2-methylphenyl) -N ² - (1-methyl-2-methylthioethyl) -3-methylsulfonyl phthalazine bromide (Compound No. 191) and N ¹ - (4-hepta fluoro-isopropyl-2-methylphenyl) -N ² - (1-
Preparation of methyl-2-methylthioethyl) -6-methylsulfonylphthalamide (Compound No. 192). N- (4-heptafluoroisopropyl-2-methylphenyl) -3-methylsulfonylphthalimide 0.63
g was dissolved in 10 ml of dioxane, and 0.25 g of 1-methyl-2-methylthioethylamine and 0.
01 g was added, and the reaction was carried out while heating under reflux for 3 hours. After completion of the reaction, the solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography using a mixed solvent of hexane / ethyl acetate = 1/1 as an eluent to give an Rf value of 0.5 to 0. Target compound of No. 7 (Compound No. 191)
The target compound (Compound N with 0.42 g and Rf value of 0.2 to 0.3)
192) 0.18 g was obtained. Physical properties: Compound No. 191 m.p. p. 205-206 ° C Yield: 55% Compound No. 192 m.p. p. 210 ~ 212 ℃ Yield: 24%

Example 3. (3-1). Preparation of 3-iodo-N- (1-methyl-3-methylthiopropyl) phthalamic acid. 3-iodophthalic anhydride 2.74 g acetonitrile 8
A solution of 1-methyl-3-methylthiopropylamine (1.19 g) in acetonitrile (3 ml) was gradually added dropwise to the ml suspension under ice cooling, and after completion of the addition, the reaction was carried out for 3 hours at room temperature with stirring. After the reaction was completed, the precipitated crystals were collected by filtration and washed with a small amount of acetonitrile to obtain 3.5 g of the desired product.
Got Physical property: m. p. 148-150 ° C Yield: 89% (3-2). Preparation of 6-iodo-N- (1-methyl-3-methylthiopropyl) phthalisoimide. To a suspension of 0.79 g of 3-iodo-N- (1-methyl-3-methylthiopropyl) phthalamide in 10 ml of toluene was added 0.63 g of trifluoroacetic anhydride, and the mixture was stirred at room temperature for 3 times.
The reaction was carried out under stirring for 0 minutes. After completion of the reaction, the solvent was distilled off under reduced pressure to obtain 0.75 g of a crude product of the desired product. The obtained target product was used in the next reaction without purification.

(3-3). 6-iodo -N ¹ - (4-heptafluoroisopropyl-2-methylphenyl) -N ² -
Production of (1-methyl-3-methylthiopropyl) phthalamide (Compound No. 162). 0.75 g of 6-iodo-N- (1-methyl-3-methylthiopropyl) phthalisoimide was added to acetonitrile 10
After dissolving in ml, 0.55 g of 4-heptafluoroisopropyl-2-methylaniline and 0.01 g of trifluoroacetic acid were added to the solution, and the reaction was carried out for 3 hours with stirring.
After the reaction was completed, the precipitated crystals were collected by filtration and washed with a small amount of cold acetonitrile to obtain 1.17 g of the desired product. Physical property: m. p. 192-194 ° C Yield: 90%

(3-4). 3-iodo -N ¹ - (4-heptafluoroisopropyl-2-methylphenyl) -N ² -
Production of (1-methyl-3-methylsulfenylpropyl) phthalamide (Compound No. 195). 6-iodo-N ^1- (4-heptafluoroisopropyl-
2-methylphenyl) -N ² - (1-methyl-3-methylthiopropyl) phthalamide 0.65g methylene chloride 1
Dissolve in 0 ml and add 0.1 ml of metachloroperbenzoic acid to the solution.
8 g was added, and the reaction was carried out at room temperature for 3 hours. After the reaction was completed, the reaction solution was poured into water, the desired product was extracted with chloroform, the organic layer was washed with an aqueous sodium thiosulfate solution and an aqueous potassium carbonate solution, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was washed with an ether-hexane mixed solvent to obtain 0.61 g of the desired product. Physical property: m. p. 123-125 ° C Yield: 92%

(3-5). 3-iodo -N ¹ - (4-heptafluoroisopropyl-2-methylphenyl) -N ² -
Production of (1-methyl-3-methylsulfonylpropyl) phthalamide (Compound No. 196). 3-iodo-N ^1- (4-heptafluoroisopropyl-
2-methylphenyl) -N ² - (1-methyl-3 by the same manner as Example methylsulfanyl phenylpropyl) phthalamide 0.4 g (3-4), the desired product 0.39g
Got Physical property: m. p. 128-130 ° C Yield: 95%

Example 4. (4-1). N- (4-heptafluoroisopropyl-
Preparation of 2-methylphenyl) -3-trifluoromethoxybenzamide. 3-Trifluoromethoxybenzoyl chloride 2.24
g was dissolved in 50 ml of tetrahydrofuran and 4 parts was added to the solution.
-Heptafluoroisopropyl-2-methylaniline (2.75 g) and triethylamine (1.2 g) were gradually added dropwise, and after completion of the addition, the reaction was carried out at room temperature for 1 hour. After completion of the reaction, the reaction solution is poured into water, the target product is extracted with ethyl acetate, dried over anhydrous magnesium sulfate, the solvent is distilled off under reduced pressure, and the obtained residue is washed with an ether-hexane mixed solvent. Thus, 4.6 g of the target product was obtained. Physical properties: oily substance. Yield: 99%

(4-2). Production of N- (4-heptafluoroisopropyl-2-methylphenyl) -3-trifluoromethoxyphthalamic acid. N- (4-heptafluoroisopropyl-2-methylphenyl) -3-trifluoromethoxybenzamide 2.
Dissolve 2g in 20ml tetrahydrofuran, -70 ° C
Then, s-butyllithium (0.96M / L) 10 was added to the solution.
After gradually adding ml and reacting at the same temperature for 30 minutes,
The cooling tank was removed, excess carbon dioxide gas was introduced into the reaction solution, and the reaction was carried out at room temperature for 30 minutes. After the reaction was completed, the reaction solution was poured into water, acidified with dilute hydrochloric acid, the desired product was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain a residue, which was then extracted with ether. 2.1 g of the target product was obtained by washing with a hexane mixed solvent. Physical property: m. p. 168-172 ° C Yield: 87%

(4-3). Preparation of N- (4-heptafluoroisopropyl-2-methylphenyl) -3-trifluoromethoxyphthalisoimide. 0.51 g of trifluoroacetic anhydride was added to a suspension of 0.46 g of N- (4-heptafluoroisopropyl-2-methylphenyl) -3-trifluoromethoxyphthalamic acid in 10 ml of toluene, and the mixture was reacted at room temperature for 30 minutes. I went. After completion of the reaction, the solvent was distilled off under reduced pressure to obtain 0.49 g of a crude product of the desired product. The obtained target product was used in the next reaction without purification. (4-4). N ^1- (4-heptafluoroisopropyl-
Preparation of 2-methylphenyl) -N ² -3- (1-methyl-2-methylthioethyl) -3-trifluoromethoxy phthalazine bromide (Compound No. 210). 0.44 g of N- (4-heptafluoroisopropyl-2-methylphenyl) -3-trifluoromethoxyphthalisoimide was dissolved in 10 ml of acetonitrile, and 1-methyl-2-methylthioethylaniline 0.10 was added to the solution.
g and 0.01 g of trifluoroacetic acid were added and reacted for 3 hours. After completion of the reaction, the reaction solution was cooled to 0 ° C., and the precipitated crystals were collected by filtration and washed with hexane to obtain 0.46 g of the desired product. Physical property: m. p. 184-185 ° C Yield: 77%

The agricultural and horticultural insecticides containing the phthalamide derivative represented by the general formula (I) or a salt thereof of the present invention as an active ingredient are various agricultural and forestry plants which damage rice, fruit trees, vegetables, other crops, flowers and the like. Suitable for horticulture, pest control such as stored-grain insects, sanitary insects, nematodes, etc., for example, apple cod beetle (Adoxophyes orana fasciata), tea beetle beetle (Adoxophyes sp.), Apple beetle (Gr)
apholita inopinata), Nasihime Shinui (Grapholita
molesta), bean squid (Leguminivora glycinivo)
rella), Kuwahamaki (Olethreutes mori) Chanohosuga (Caloptiliathevivora), Apple Hosogah (Caloptili)
a zachrysa), kinmonhosoga (Phyllonorycter ring)
oniella), Pear moth (Spulerrina astaurota), Pieris rapae crucivora (Piers rapae crucivora), Helicoverpa armigera (Heliothis sp.), Codling moth (Laspey resia p)
omonella), diamondback moth (Plutella xylostella), apple apple squirrel (Argyresthia conjugella), peach mosquito (Carposina niponensis), lizard (Chilo su)
ppressalis), Cobb Nomeiga (Cnaphalocrocis medinal)
is), Chamadalameiga (Ephestia elutella), Kwanomaiga (Glyphodes pyloalis), Sankamaiga (Scir)
pophaga incertulas), Parrotara gu
ttata), armyworm (Pseudaletia separata),

Lepidoptera insect pests such as rice armyworm (Sesamia inferens), red-spotted armyworm (Spodoptera litura), white-spotted armyworm (Spodoptera exigua), etc.
rvata lugens), White-faced planthopper (Sogatella furcifer)
a), orange whitefly (Diaphorina citri), grape whitefly (Aleurolobus taonabae), tobacco whitefly (Bemisia tabaci), whitefly whitefly (Trialeurod)
es vaporariorum), Falcons (Lipaph)
is erysimi), Myzus persica
e), black weevil (Ceroplastes ceriferus), citrus scale insect (Pulvinaria aurantii), citrus insect scale bug (Pseudaonidia duplex), pit insect scale bug (Comstockaspis perniciosa), stag beetle (Unaspis yanonenoptera), etc. (Pratylenchus sp.), Japanese beetle (Anomala rufocuprea), Japanese beetle (Popillia japon)
ica), tobacco beetle (Lasioderma serricorne)
), Flatworm Beetle (Lyctus brunneus), Red-tailed Spodoptera (Epilachna vigintiotopunctata),
Azuki bean weevil (Callosobruchus chinensis),

Weevil Weevil (Listroderes costirostr
is), weevil (Sitophilus zeamais), boll weevil (Anthonomus gradis gradis), rice weevil (Lissorhoptrus oryzophilus), weevil (Aula)
cophora femoralis), Rice budworm (Oulema ory)
zae), the leaf beetle (Phyllotreta striolata)
), Pine beetle (Tomicus piniperda), Colorado potato beetle (Leptinotarsa decemlineata),
Mexican Bean Beetle (Epilachna varivestis),
Coleopteran insects such as corn rootworms (Diabrotica sp.), Sea fly (Dacus (Zeugodacus) cucurbitae), mandarin fruit fly (Dacus (Bactrocera) dorsalis), rice leaf fly (Agromyza oryzae), onion fly (Deli)
a antiqua), sand fly (Delia platura), soybean fly (Asphondylia sp.), house fly (Musca do)
Mestica), Culex pipiens pipiens)
us coffeae), potato cyst nematode (Globoder)
a rostochiensis), root-knot nematode (Meloidogyne)
sp.), citrus nematode (Tylenchulus semipenetr)
ans), Narcissus communis (Aphelenchus avena
e), spinach (Aphelenchoides ritzemabos)
It has a strong insecticidal effect against the nematode pests such as i).

The agricultural and horticultural insecticide containing the phthalamide derivative represented by the general formula (I) or a salt thereof of the present invention as an active ingredient damages paddy field crops, field crops, fruit trees, vegetables, other crops and flowers. Since it has a remarkable control effect against the pests to give, in accordance with the time when the occurrence of pests is predicted, before the occurrence of pests or at the time when the occurrence is confirmed, paddy fields, fields, fruit trees, vegetables, Other crops, flower seeds,
The desired effect of the agricultural and horticultural insecticide of the present invention can be obtained by treating the plant such as foliage or the like, the growing environment such as paddy water or soil.

The plant to which the agricultural and horticultural insecticide of the present invention can be used is not particularly limited, but examples thereof include the plants shown below. Cereals (eg, rice, barley, wheat, rye, oats, corn, etc.), beans (soybeans, red beans, broad beans, peas, kidney beans, peanuts, etc.), fruit trees / fruits (apples, citrus fruits, pears, grapes) , Peach, plum, yellow peach,
Walnuts, chestnuts, almonds, bananas, strawberries, etc.), leaves and fruits (cabbage, tomato, spinach, broccoli,
Lettuce, onion, leek, pepper, eggplant, pepper, etc., root vegetables (carrot, potato, sweet potato, taro, radish, lotus root, turnip, burdock, garlic, etc.), processing crops (coffin, hemp, beets, hops, sugar cane) , Sugar beet, olive, rubber, coffee, tobacco, tea, etc., melons (pumpkin, cucumber, makuwari, watermelon, melon, etc.), grasses (orchard grass, sorghum, timothy, clover, alfalfa, etc.), turf (Koryo) Turf,
Bentograss, etc.), fragrances and other crops for appreciation (lavender, rosemary, thyme, parsley, pepper, ginger, etc.), flowers (chrysanthemums, roses, carnations, orchids, etc.), garden trees (gingko, sakura, aoki etc.), forest trees (Todomatsu, Ezomatsu, Pine, Hiba, Japanese cedar, Japanese cypress, etc.)

The agricultural and horticultural insecticide of the present invention is used as it is for controlling various pests, or is appropriately diluted or suspended in water or the like in an amount effective for controlling pests or nematodes to obtain the pests and the line. It may be used for plants in which the occurrence of insects is predicted. For example, for pests and nematodes that occur in fruit trees, cereals, vegetables, etc., in addition to spraying on the foliage, immersion of seeds in a drug, seed dressing , Seed treatment such as calper treatment, soil whole layer mixing, row application, soil mixing, cell seedling treatment,
Planting hole processing, stock processing, top dress, rice box processing,
It can also be used after being applied to the surface of the water such as application to the surface of the water and absorbed from the roots. In addition, application to nutrient solution in nutrient solution (hydroponics) cultivation, use by smoking or stem injection, etc. can also be performed. Further, the agricultural and horticultural insecticide of the present invention may be used as it is, or may be appropriately diluted with water or the like, or may be used in a suspended form in an amount effective for controlling pests at the place where the occurrence of the pests is predicted. , For example storage pests, house pests, sanitary pests,
In addition to being sprayed on forest pests, it can also be applied to house building materials, smoke, bait, etc.

The seed treatment method is, for example, a method in which a liquid or solid preparation is diluted or undiluted to immerse the seed in a liquid state so as to penetrate the drug, and a solid preparation or a liquid preparation is mixed with the seed. Examples thereof include a method of applying a dressing treatment to attach the seed to the surface of the seed, a method of mixing with an adhesive carrier such as a resin or a polymer to coat the seed, and a method of spraying in the vicinity of the seed at the same time as planting. The "seed" for performing the seed treatment means a plant in the early stage of cultivation used for the propagation of plants, for example, other than seeds, bulbs, tubers, seed potatoes, plant buds, baskets, bulbs, or for cuttings cultivation. Plants for vegetative propagation can be mentioned. The "soil" or "cultivation carrier" of a plant when carrying out the method of use of the present invention is a support for cultivating a crop, particularly a support for growing roots, and the material is not particularly limited. However, so long as the plant can grow, it may be so-called soil, seedling mat, water, etc. Specific materials include, for example, sand, pumice, vermiculite, diatomaceous earth, agar, gel-like substances, high It may be a molecular substance, rock wool, glass wool, wood chips, bark or the like.

As a method for spraying crop foliage or stored grain pests, house pests, sanitary pests, forest pests, etc., emulsion,
A liquid preparation such as a flowable agent or a solid preparation such as a wettable powder or a granular wettable powder may be appropriately diluted with water and then sprayed, a method of spraying a powder, or smoke. As a method for applying to soil, for example, a method of applying a liquid formulation to a plant base or a nursery for raising seedlings without diluting it in water, a granule for a plant base or raising seedlings Method of spraying on seedbed etc., method of spraying powder, wettable powder, wettable granules, granules, etc. before seeding or transplanting and mixing with the whole soil, planting hole before planting or planting, planting Examples thereof include a method in which a powder, a wettable powder, a wettable granule, a granular powder or the like is sprayed on the strip or the like.

As a method of applying paddy rice to a nursery box, the dosage form may vary depending on the application time such as application at seeding, application at greening period, application at transplanting, etc. It may be applied in a dosage form such as. It can also be applied by mixing with the soil, and can be mixed with the soil and the powder, the wettable granules or the granules, for example, the soil in the soil, the soil in the soil, or the entire soil. The culture medium and various preparations may be applied alternately in layers. As a method of applying to paddy fields, solid preparations such as jumbo preparations, pack preparations, granules and wettable granules, and liquid preparations such as flowables and emulsions are usually sprayed on flooded paddy fields. In addition, at the time of planting rice, an appropriate formulation can be used as it is, or can be mixed with fertilizer and sprayed and injected into the soil. Further, by using a chemical solution such as emulsion or flowable as a source of water flowing into a paddy field such as a water spout or an irrigation device, it can be applied labor-savingly as water is supplied.

[0125] In field crops, a cultivation carrier or the like in the vicinity of seeds or plants can be treated during the period from sowing to raising seedlings. For plants to be sown directly in the field, in addition to direct treatment of seeds, treatment of the plant origin of the plant being cultivated is preferable. It is possible to perform a spraying treatment using a granule or an irrigation treatment in a liquid form with a drug diluted or not diluted with water. It is also a preferable treatment to mix the granules with the cultivation carrier before sowing and then sow. As the sowing of the cultivated plants to be transplanted and the treatment at the seedling raising stage, in addition to direct treatment of seeds, irrigation treatment of liquid medicine or spray treatment of granules to seedbeds for raising seedlings is preferable. In addition, it is also preferable to treat the planting holes with granules at the time of planting, or to mix them with the cultivation carrier in the vicinity of the transplanting place. The agricultural and horticultural insecticide of the present invention is generally used by formulating it into a form convenient for use according to a conventional method for pesticide formulation. That is, the phthalamide derivative represented by the general formula (I) is dissolved, separated, suspended, mixed, by mixing these in an appropriate inert carrier, or if necessary, together with an auxiliary agent in an appropriate ratio, Impregnating, adsorbing or adhering, appropriate dosage form,
For example, it may be used by formulating it into a suspension, emulsion, liquid, wettable powder, granule, powder, tablet and the like.

The inert carrier that can be used in the present invention may be either solid or liquid, and examples of the material which can be a solid carrier include soybean flour, cereal flour, wood flour, bark flour, sawdust powder, Tobacco stem powder, walnut shell powder, bran, fibrin powder, residue after extraction of plant extracts, synthetic polymers such as ground synthetic resin, clays (eg kaolin, bentonite, acid clay, etc.), talcs (eg talc, pyrophyllide) Etc.), silicas (for example, diatomaceous earth, silica sand, mica, white carbon [hydrogenated finely divided silicon, synthetic highly dispersed silicic acid also called hydrous silicic acid, and some products contain calcium silicate as a main component]), activated carbon, sulfur powder , Pumice stone, calcined diatomaceous earth, brick crushed product, fly ash, sand, calcium carbonate, inorganic mineral powder such as calcium phosphate, ammonium sulfate,
Examples thereof include chemical fertilizers such as ammonium phosphate, ammonium nitrate, urea, ammonium chloride, and compost, which are used alone or in the form of a mixture of two or more kinds.

The material which can be used as a liquid carrier is selected from those having solvent ability per se, and those having no solvent ability but capable of dispersing an active ingredient compound with the aid of an auxiliary agent. Typical examples of the carrier include the following, which are used alone or in the form of a mixture of two or more kinds, for example, water, alcohols (for example, methanol, ethanol, isopropanol, butanol, ethylene glycol, etc.), ketones. (For example, acetone, methyl ethyl ketone, methyl isobutyl ketone,
Diisobutyl ketone, cyclohexanone, etc.), ethers (eg ethyl ether, dioxane, cellosolve,
Dipropyl ether, tetrahydrofuran etc.), aliphatic hydrocarbons (eg kerosene, mineral oil etc.), aromatic hydrocarbons (eg benzene, toluene, xylene, solvent naphtha, alkylnaphthalene etc.), halogenated hydrocarbons (eg dichloroethane) , Chloroform, carbon tetrachloride, chlorinated benzene, etc.), esters (eg ethyl acetate, diisopropyl phthalate, dibutyl phthalate, dioctyl phthalate etc.), amides (eg dimethylformamide, diethylformamide, dimethylacetamide etc.) , Nitriles (for example, acetonitrile), dimethyl sulfoxides, and the like.

As other auxiliary agents, there can be mentioned the representative auxiliary agents exemplified below, and these auxiliary agents are used depending on the purpose, and they may be used alone or, in some cases, in combination of two or more kinds. However, in some cases it is also possible to use no adjuvant at all. A surfactant is used for the purpose of emulsifying, dispersing, solubilizing and / or wetting the active ingredient compound, for example, polyoxyethylene alkyl ether, polyoxyethylene alkylaryl ether, polyoxyethylene higher fatty acid ester, polyoxyethylene. Resin acid ester, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monooleate, alkyl aryl sulfonate, naphthalene sulfonic acid condensate,
Examples thereof include surfactants such as lignin sulfonate and higher alcohol sulfate. In addition, for the purpose of stabilizing the dispersion of active ingredient compounds, adhering and / or binding, auxiliary agents exemplified below can be used, for example, casein, gelatin, starch, methyl cellulose, carboxymethyl cellulose, gum arabic, polyvinyl. Auxiliary agents such as alcohol, pine oil, bran oil, bentonite, lignin sulfonate and the like can also be used.

The following auxiliaries can be used for improving the fluidity of the solid product, for example, waxes, stearates, alkyl phosphates and the like. As a deflocculant for a suspending product, an auxiliary agent such as a naphthalenesulfonic acid condensate or a condensed phosphate can be used. As the defoaming agent, for example, an auxiliary agent such as silicone oil can be used. The compounding ratio of the active ingredient compound can be adjusted as necessary, and may be appropriately selected from the range of 0.01 to 80% by weight relative to 100% by weight of the composition. For example, in the case of powder or granules 0.0
1 to 50% by weight, and 0.01 to 50% by weight is also suitable when the emulsion or wettable powder is used. The agricultural and horticultural insecticide of the present invention is used as it is for controlling various pests, or is appropriately diluted with water or the like, or is suspended in a form effective for disease control in a form in which the occurrence of the pests is predicted. Alternatively, it may be used by applying it to a place where generation is not preferable.

The use amount of the agricultural and horticultural insecticide of the present invention depends on various factors such as purpose, target pests, crop growth status, pest development tendency, weather, environmental conditions, dosage form, application method, application site, and application. Although it varies depending on the time and the like, the active ingredient compound may be appropriately selected from the range of 0.1 g to 10 kg per 10 are depending on the purpose. Agricultural and horticultural insecticides of the present invention are further pesticides to be controlled, for the purpose of expanding a suitable period for control, or to reduce the dose, and for the purpose of achieving a synergistic effect, other agricultural and horticultural insecticides, acaricides and nematicides. It is also possible to use it as a mixture with a fungicide, a biopesticide or the like, or it can be used as a mixture with a herbicide, a plant growth regulator, a fertilizer or the like depending on the use scene.

Other agricultural and horticultural insecticides, acaricides and nematicides used for such a purpose include, for example, ethione, trichlorfon, methamidophos, acephate, dichlorvos, mevinphos, monocrotophos, malathion, dimethoate, formothione, mecarbam. , Bamidothion,
Thiometone, disulfoton, oxydeprophos, nared, methylparathion, fenitrothion, cyanophos, propaphos, fenthion, prothiophos, profenophos, isofenphos, temephos, fentoate, dimethylvinphos, chlorfevinphos, tetrachlorvinphos, hoxime, isoxathion, pyraclofos, Methidathion, Chloropyrifos, Chlorpyrifos
Methyl, pyridafenthion, diazinon, pirimiphos-methyl, fosalone, phosmet, dioxabenzophos, quinalphos, terbufos, etoprophos, kazusaphos, mesulfenphos, DPS (NK-0795), phosphocarb, fenamiphos, isamidophos, fostiazate, isazophos, enaprophos, phenthione, phosthione, phosphine, fothion Diclofenthion, thionazine, sulprophos, fensulfothion, diamidaphos, pyrethrin, allethrin,

Praletrin, resmethrin, permethrin, tefluthrin, bifenthrin, fenpropatrine, cypermethrin, alpha cypermethrin, cyhalothrin, lambda cyhalothrin, deltamethrin, acrinathrin, fenvalerate, esfenvalerate, flucitrinate, fluvalinate, cycloprothrin. Trin, Etofenprox, Halfenprox,
Silafluofen, flucitrinate, fluvalinate, mesomil, oxamyl, thiodicarb, aldicarb, alanicalub, cartap, metolcarb, xilicarb, propoxur, phenoxycarb, fenobucarb, etiophencarb, phenothiocarb, bifenazeto, BPMC, carbaryl, carmifurfan, carbofuran, carbofuran. Fratiocarb, benfuracarb, aldoxicarb, diafenthiuron, diflubenzuron, teflubenzuron, hexaflumuron, novalron, rufenuron, flufenoxuron,
Chlorfluazuron, fenbutatin oxide, tricyclohexyltin hydroxide, sodium oleate, potassium oleate, methoprene, hydroprene, vinapacryl, amitraz,

Dicofol, quelsen, chlorbenzilate, phenisobromolate, tetradiphone, bensultap, benzoate, tebufenozide, methoxyphenozide, chromafenozide, propargit, acequinocyl, endosulfan, diofenolan, chlorfenapyr, fenpyroximate, tolfenpyrad, fipronil, tepfenademate, tebufenate, febupronil, teffenafene, tebufenate. Hexithiazox, nicotine sulfate, nitenpyram, acetamiprid, thiacloprid, imidacloprid, thiamethoxam, clothianidin, nidinotefuran, fluazinam, pyriproxyfen, hydramethylnon, pyrimidifen, pyridaben, cyromazine, TP
IC (tripropyl isocyanurate), pymetrozine, clofentezine, buprofezin, thiocyclam, fenazaquin, quinomethionate, indoxacarb, polynactin complex, milbemectin, abamectin, emamectin benzoate, spinosad, BT
(Bacillus thuringiensis), Azadirachtin,
Chloronicotinyl compounds such as rotenone, hydroxypropyl starch, levamisole hydrochloride, metam sodium, morantel tartrate, dazomet, trichlamide, bastria, monacrosporium fimatopa gum, albendazole, oxybendazole, oxfenzazole, fenbendazole, etc. , Carbamate compounds, pyrethroid compounds, macrolide compounds, organic phosphorus compounds, agricultural and horticultural insecticides, acaricides or nematicides.

Examples of agricultural and horticultural fungicides used for the same purpose include, for example, sulfur, lime-sulfur mixture, basic copper sulfate, iprobenphos, edifenphos, tolclofos-methyl, thiram, polycarbamate, zineb, manzeb, mancozeb. , Propineb, thiophanate, thiophanate methyl, benomyl, iminoctazine acetate, iminoctadine albesylate, mepronil, flutolanil, penciclone, flametopyr, tifluzamide, metalaxyl, oxadixyl, carpropamide, diclofluanid, fursulfamide, chlorothalonil, N-cresoxamyl N, cresoxinmethyl, N -9425), hymexazole, eclomezole, fluorimide, procymidone, vinclozolin, iprodione, triadimefone, triflumiso. , Bittertanol, triflumizole, ipconazole, fluconazole, propiconazole, difenoconazole, microbutanyl, tetraconazole, hexaconazole, tebuconazole, imibenconazole, prochloraz, pefurazoate, cyproconazole, isoprothiolane, fenarimol, pyrimethanil, mepanipyrimyl, mepanipyramil, mepanipyramil. Phenox, fluazinam, triphorin, diclomedine, azoxystrobin,
Examples of agricultural and horticultural fungicides such as thiadiazine, captan, probenazole, acibenzofural-S-methyl (CGA-245704), fusaride, tricyclazole, pyroquilon, quinomethionate, oxolinic acid, dithianon, kasugamycin, validamycin, polyoxin, blasticidin, streptomycin. You can

Similarly, as herbicides, for example, glyphosate, sulfosate, glufosinate, bialaphos, butamiphos, esprocarb, prosulfocarb, benchocarb, pyributicarb, ashram, linuron, dimuron, bensulfuron-methyl, cyclosulfamurone, cynosulfuron, pyra. Zosulfuron ethyl, azimuthulfuron, imazosulfuron, tenyl chlor, alachlor, pretilachlor, cromeprop, ethobenzanide, mefenacet, pendimethalin, bifenox, acifluofen, lactofen, cyhalofop-butyl, aioxynil, bromobutide, alloxydim, cetoxidin, napropamide, napropamide. Pyrazolate, benzophenap, pyraflufen-ethyl, imaza Le, sulfentrazone, cafe down stroke - le, Bentokisazon, Okisazoazon, paraquat, diquat, pyriminobac, simazine, atrazine, dimethametryn, triaziflam, benfuresate, Furci asset-methyl, quizalofop-ethyl,
Examples thereof include compounds having herbicides such as bentazone and calcium peroxide, but the present invention is not limited thereto. Note that the above compound names are generic names except for special notes.

Examples of biological pesticides include nuclear polyhedrosis virus (NPV), granulosis virus (GV), cytoplasmic polyhedrosis virus (CPV), insect pox virus (Entomopox). virus, EPV) and other virus preparations, Monosporium fimatopa gum (Mona
crosporium phymatophagum), Steinernema carpocapsae, Steinernema kushidai, Pasteuria penetrans, and other microbial pesticides and trichoderma used as nematicides.
Lignolan (Trichoderma lignorum), Agrobacterium radiobactor
), Non-pathogenic Erwinia carotobora (Erwinia car
otovora), Bacillus subtilis
The same effect can be expected by mixing with a microbial pesticide used as a bactericide such as) and a biopesticide used as a herbicide such as Xanthomonas campestris.

Further, as biological pesticides, for example, Oncaria wasps (Encarsia formosa), Coleman velvet (Ap
hidius colemani), gypsy fly (Aphidoletes)
aphidimyza), Yellow-bellied wasp (Diglyphus isaea)
), Mosquito beetle (Dacnusa sibirica), dust mite (Phytoseiulus persimilis), Amblyseius cucumeris, and other natural creatures such as Orius sauteri, Boberia
Microbial pesticides such as Beauveria brongniartii, (Z) -10-tetradecenyl acetate,
(E, Z) -4,10-Tetradecadiniel = acetate. (Z) -8-dodecenyl = acetate. (Z) -1
1-tetradecenyl = acetate. (Z) -13-icosen-10-one, (Z) -8-dodecenyl = acetate. (Z) -11-tetradecenyl = acetate.
(Z) -13-icosen-10-one.14-methyl-
It is also possible to use it together with a pheromone agent such as 1-octadecene.

Agro-horticultural pest control in which a phthalamide derivative represented by the general formula (I) of the present invention or a salt thereof and one or more compounds selected from the above-mentioned second active ingredient compounds are combined. Control agent 100
The amount of the active ingredient compound added is 0.1 part by weight to 5 parts by weight.
It may be used by appropriately selecting from the range of 0 parts by weight, and preferably in the range of 1 part by weight to 20 parts by weight. Further, the phthalamide derivative represented by the general formula (I) in the active ingredient compound or a salt thereof and other agricultural and horticultural insecticides, acaricides, nematicides,
The addition ratio of the active ingredient compound selected from a fungicide, a herbicide or a biological pesticide is 1% by weight of the phthalamide derivative or a salt thereof for other agricultural and horticultural insecticides, acaricides, nematicides, sterilizers. The active ingredient compound selected from the agents, herbicides or biological pesticides may be appropriately selected and used from the range of 0.05 to 2000 parts by weight, preferably 10 to 100 parts by weight. .

Typical examples and test examples of the present invention are shown below, but the present invention is not limited to these.
In the formulation examples, “part” means “part by weight”. Formulation Example 1. Compound shown in Table 1, 2 or 3 50 parts Xylene 40 parts Mixture of polyoxyethylene nonylphenyl ether and calcium alkylbenzene sulfonate 10 parts The above components are uniformly mixed and dissolved to obtain an emulsion. Formulation example 2. Compounds described in Table 1, 2 or 3 3 parts Cray powder 82 parts Diatomaceous earth powder 15 parts The above are uniformly mixed and pulverized to obtain a powder.

[0140] Formulation example 3.   5 parts of the compounds listed in Table 1, 2 or 3   90 parts mixed powder of bentonite and clay   Calcium lignin sulfonate 5 parts     Mix the above uniformly, add an appropriate amount of water and knead, granulate and dry to make granules . Formulation example 4.   20 parts of the compounds listed in Table 1, 2 or 3   Kaolin and synthetic highly dispersed silicic acid 75 parts   Polyoxyethylene nonylphenyl ether and al   Mixture with calcium benzene sulfonate 5 parts     The above is uniformly mixed and pulverized to obtain a wettable powder.

Test Example 1. Diamondback moth (Plutella xylostella)
(1) The Chinese cabbage seedlings are released into adult ovipositors and laid to lay eggs, and two days after the release, the Chinese cabbage seedlings with laying eggs are placed in the first, second or third.
A drug containing the compound shown in the table as an active ingredient is immersed in a drug solution diluted to 50 ppm for about 30 seconds, and air-dried at 25 ° C at 25 ° C.
It was left to stand in a constant temperature room at ℃. Six days after the immersion in the chemical solution, the number of hatched worms was examined, the mortality rate was calculated by the following formula, and the judgment was made according to the following criteria. 1 ward 10 heads 3 stations The results are shown in Tables 5 and 6.

Test Example 2. Spodoptera l
Insecticide test against itura) Cabbage leaf pieces (variety: four season harvest) are soaked for about 30 seconds in a chemical solution diluted with a drug containing the compound shown in Table 1, 2 or 3 as an active ingredient for about 30 seconds, and after air-drying, a plastic petri dish having a diameter of 9 cm After inoculating with the second-instar larva of Spodoptera litura, it was capped and allowed to stand in a thermostatic chamber at 25 ° C. Eight days after the inoculation, the number of live and dead insects was examined, the mortality rate was calculated by the following formula, and the judgment criteria were according to Test Example 1. 1 ward 3
Continuation The results are shown in Tables 5 and 6.

Test Example 3. Chanoco Kakumon Hamaki (Adox
insecticidal test against ophyes sp.). Tea leaves were soaked for about 30 seconds in a drug solution prepared by diluting a drug containing the compound shown in Table 1, 2 or 3 as an active ingredient to 50 ppm, and after air-drying, the tea leaves were placed in a plastic petri dish having a diameter of 9 cm and inoculated with the larvae of Pleurotus cornucopiae. After 25
It was left to stand in a constant temperature room at 70 ° C and a humidity of 70%. The number of live and dead insects was examined 8 days after the inoculation, and the number was determined according to the criteria of Test Example 1. Tables 5 and 6 show the results of the three-group control of 10 horses in one ward.

[0144]

[0145]

[0146]

[0147]

[0148]

[0149]

[0150]

[0151]

[0152]

[0153]

[0154]

[0155]

[0156]

[0157]

[0158]

[0159]

[0160]

[0161]

[0162]

[0163]

[0164]

[0165]

[0166]

Then, a phthalamide derivative represented by the general formula (I) of the present invention or a salt thereof and other agricultural and horticultural insecticides, acaricides, nematicides, agricultural and horticultural fungicides, and herbicides are given below. Alternatively, representative formulation examples and test examples when combined with a biological pesticide are illustrated, but the present invention is not limited thereto. In the formulation examples, “part” means “part by weight”. Formulation Example 5 Compounds described in Table 1, 2 or 3 5 parts Fenpyroximate 10 parts Hydrous silicic acid 30 parts Hitenol M08 (manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) 5 parts Calcium lignin sulfonate 3 parts Wettable clay 47 parts Active ingredient compound After impregnating with hydrous silicic acid, it is uniformly mixed with other components to obtain a wettable powder.

Formulation Example 6 Compounds shown in Table 1, 2 or 3 10 parts Tebufenpyrad 10 parts NPE-100 (manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) 20 parts Propylene glycol 5 parts Rhodopol 23 (manufactured by Rhone-Poulin) 2 parts Water 43 The above parts are uniformly mixed and dispersed in water to obtain a flowable agent. Formulation Example 7 Compounds described in Table 1, 2 or 3 10 parts Isoprothiolane 20 parts Hydrous silicic acid 20 parts SP-3005X (manufactured by Toho Kagaku) 30 parts Demol T (manufactured by Kao Atlas) 10 parts Xylene 10 parts or more uniformly mixed and melted To make an emulsion.

Formulation Example 8 Compounds listed in Table 1, 2 or 3 10 parts tebufenozide 20 parts NPE-100 20 parts propylene glycol 2 parts rhodopol 23 1 part water 47 parts The above ingredients are uniformly mixed and dispersed in water to obtain a flowable mixture. Use as an agent. Formulation Example 9 Compounds described in Table 1, 2 or 3 10 parts Buprofezin 5 parts Hydrous Silicic Acid 34 parts Hytenol M08 3 parts Demol T 2 parts Calcium Carbonate Powder 46 parts After impregnating hydrous silicic acid with the active ingredient compound, The ingredients are uniformly mixed to obtain a wettable powder.

Formulation Example 10 Compounds shown in Table 1, 2 or 3 10 parts Pyridaben 15 parts Hydrous silicic acid 20 parts SP-3005X 30 parts Demol T 5 parts Xylene 20 parts The above ingredients are uniformly mixed and melted to give an emulsion. Formulation Example 11 Compounds described in Table 1, 2 or 3 10 parts Pyraflufenethyl 20 parts NPE-100 20 parts Propylene glycol 2 parts Rhodopol 23 0.5 parts Water 47.5 parts The above components are uniformly mixed and added to water. Disperse into a flowable agent.

Formulation Example 12 Compounds shown in Table 1, 2 or 3 10 parts Acetamiprid 5 parts NPE-100 34 parts Propylene glycol 3 parts Rhodopol 23 2 parts Water 46 parts The above ingredients are uniformly mixed and dispersed in water to be flowable. Use as an agent. Formulation Example 13 Compounds shown in Table 1, 2 or 3 10 parts Imidacloprid 10 parts Hydrous silicic acid 25 parts SP-3005X 30 parts Demol T 5 parts Xylene 20 parts The above ingredients are uniformly mixed and melted to obtain an emulsion.

Formulation Example 14 Compounds listed in Tables 1, 2 or 3 5 parts Chlorfenapyr 10 parts NPE-100 35 parts Propylene glycol 3 parts Rhodopol 23 2 parts Water 45 parts The above ingredients are uniformly mixed and dispersed in water to be flowable. Use as an agent. Formulation Example 15 Compound shown in Table 1, 2 or 3 5 parts Pymetrozine 10 parts NPE-100 35 parts Propylene glycol 3 parts Rhodopol 23 2 parts Water 45 parts The above components are uniformly mixed and dispersed in water to obtain a flowable agent. .

Test Example 4. Insecticidal test against Chacococca esculentris Tea leaves are soaked in a chemical solution diluted to a predetermined concentration for 30 seconds, air-dried, and then placed in a plastic petri dish with a diameter of 9 cm.
Chanoco Kakumonhamaki 4th inoculated 10 heads each, 25 ℃
It was left standing in a constant temperature room. After 4 and 7 days of treatment, the number of surviving worms was examined and the mortality rate was calculated (1 ward, 10 heads, 2 stations). The results are shown in Table 7.

[0174]

Test Example 5. Insecticidal test against green peach aphid Chinese cabbage (variety: Aichi) was planted in a plastic pot having a diameter of 8 cm and a height of 8 cm, and the green peach aphid was bred. After air-drying, the pots were allowed to stand in a greenhouse, and 6 days after spraying, the number of aphids parasitic on each Chinese cabbage was examined, and the control value was calculated according to the following criteria (1 ward, 1 pot, 2 consecutive controls). [Equation 3] Control value = 100 − {(Ta × Cb) / (Tb × Ca)} × 100 Ta: Number of parasites after spraying in treated area Tb: Number of parasites before spraying in treated area Ca: In untreated area Number of parasites after spraying Cb: Table 8 shows the results of the number of parasites before spraying in the untreated section.

[0176]

Test Example 6. Insecticidal test against brown planthopper Rice seedlings (variety: Nipponbare) are dipped in a chemical solution diluted to a predetermined concentration for 30 seconds, air-dried, and then put into a glass test tube (diameter 1.8 cm, height 20 cm). After inoculating each of them, a cotton plug was applied. The number of survivors was examined 1 and 4 days after the treatment, and the mortality rate was calculated (1 ward, 10 heads, 2 consecutive systems). The results are shown in Table 9.

[0178]

Test Example 7. Insecticidal test against resistant spider mites Fill a plastic cup 8 cm in diameter with water and
A lid having a cm hole was placed, a filter paper with a part of a cut was placed on the top of the lid, and the filter paper was suspended from the lid in water so that the filter paper was always wet due to a capillary phenomenon. Green bean leaves (variety:
Make a leaf disk with a diameter of 2 cm using Top Crop) and place it on the filter paper.
0 head was inoculated, 50 ml of the drug solution diluted to a predetermined concentration was evenly sprayed on the turntable, and after spraying, it was left standing in a thermostatic chamber at 25 ° C. Two days after the treatment, the number of surviving worms was examined and the mortality rate was calculated (10 pups in 1 ward, 2 stations). The results are shown in Table 10.

[0180]

Test Example 8. Effect test on sweet potato root-knot nematode 2 kg of root-knot nematode-contaminated soil and a prescribed amount of granules were mixed, filled in a 1 / 5000a Wagner pot, seeded with melon seeds, and after standing, left in a greenhouse. After 60 days of treatment, 25 g of soil was collected, nematodes were separated by the Bellmann method, and 48 hours later, investigation was carried out (1 ward, 1 pot, 2 pots).
Continuous control). The results are shown in Table 11.

[0182]

Test Example 9. Rice weevil and rice blast control test by applying a rice seedling box Rice (cultivar: Koshihikari) cultivated in a seedling box was treated with 50 g of granules per box and then transplanted to Honda on the same day (5
Mid-month). The control effect against rice weevil is transplantation 2
One day later, the number of shares of each 100 wards in each ward was investigated and the degree of damage was calculated. The effect on rice blast is transplantation 6
After 0 days, the lesion area ratio was investigated and judged.

[Formula 4] Damage level = {(4A + 3B + 2C + D) / (4 ×
N)} × 100 A: Damaged leaf rate of 91% or more B: Damaged leaf rate of 61 to 90% C: Damaged leaf rate of 31 to 60% D: Damaged leaf rate of 1 to 30% N: The number of surveyed strains is shown in Table 12. Show.

[0184]

Test Example 10. Tests for control of Astragalus chinensis and Kobnomigaiga by applying rice seedling boxes to rice (variety: Nihonbare) treated with 50 g of granules per box and then transplanted to Honda (mid-May).
For the control effect on Aedes mosquitoes, 40 days after transplantation, 60 days after transplantation, the number of parasites was examined for 30 strains in each ward, and for the control effect on Kobnomigae, the number of damaged leaves was investigated for 100 strains in each ward 50 days after transplantation, and the damaged leaf rate was calculated. The results are shown in Table 13.

[0186]

Test Example 11. Test for control of diamondback moth and rotifer by soil treatment of kanran Soil mixed with bed soil in a cell seedling box and seeded with kanran (variety: YR Seitoku), or treated during extraction of true leaves of kanran planted with cell seedling, or Immediately before planting, treatment was carried out at the time of planting, or plant treatment was carried out after planting. The number of parasites per 30 strains was investigated 21 days after transplantation in both diamondback moth and P. trochanterus (late June). The results are shown in Table 14.

[0188]

Note) The effect of benfuracarb alone and mixed use could not be determined due to the influence of drug damage. Test Example 12. Test of the effect of beet on Spodoptera porcine: Beet in a paper pot (variety: Monoace S)
Then, the drug solution diluted to a predetermined concentration was irrigated with 3 L, and immediately after that, it was planted. After planting, the number of damaged strains per 100 shares per ward was investigated on a predetermined day. The results are shown in Table 15.

[0190]

Test Example 13. Pest control test against Erythrium occidentalis in combination with natural enemy pesticides Eggplant (Senryo No. 2) with occidentalis thrips in a greenhouse was sprayed with a chemical solution diluted to a predetermined concentration on a shoulder spreader, and after air-drying, Kukumelis 100 mites were released per strain. After 14 days, 21 days, and 28 days after the treatment, the number of thrips and Kukumarisuka mites per top 20 leaves was investigated (early June). The results are shown in Table 16.

[0192]

[0193]

INDUSTRIAL APPLICABILITY The phthalamide derivative represented by the general formula (I) or a salt thereof according to the present invention exhibits an excellent control effect as an agricultural and horticultural insecticide, and it is also an agricultural and horticultural insecticide,
An excellent controlling effect can be obtained by using it together with an acaricide, a nematicide, a fungicide, a herbicide, a plant growth regulator, a biopesticide or the like.

─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. ⁷ Identification code FI theme code (reference) A01N 43/18 A01N 43/18 Z 4H011 43/36 43/36 C 43/40 101 43/40 101E 101J 43 / 54 43/54 D 43/56 43/56 BC 43/58 43/58 B 43/707 43/707 43/78 43/78 A 43/824 43/84 102 43/84 102 43/88 43 / 88 101 101 47/24 C 47/24 Z 47/34 47/34 51/00 51/00 55/00 D 53/06 55/04 F 53/12 57/16 102B 55/00 105A 55/04 57 / 28 F 57/16 102 63/02 B 105 C07C 317/28 57/28 C07D 213/61 63/02 213/64 C07C 317/28 213/70 C07D 213/61 213/71 213/64 239/38 213 / 70 277/04 213/71 277/76 239/38 295/18 Z 277/04 333/36 277/76 333/48 285/125 A01N 43/82 101C 295/18 53/00 506A 333/36 510 333 / 48 C07D 285/12 D (72) Inventor Tatsuki Nishida 3-7-22-202 Koda, Tomitabayashi, Osaka (72) Inventor Takashi Furuya 2821 Hineno, Izumisano, Osaka (72) Inventor Toshiaki Shimizu, Kawachinagano, Nagano, Osaka Tomachi 974-90-303 (72) Inventor Akira Seo 2-3-19 Kiimigaoka, Hashimoto-shi, Wakayama (72) Inventor Kazuyuki Sakata 5-6-301 Honda-cho, Kawachinagano-shi, Osaka (72) Inventor Shinsuke Fujioka 1-28 Nishinoyama-cho, Kawachinagano-shi, Osaka (72) Inventor Hideo Sugano 3-2-1-2-Shirakawa, Ibaraki-shi, Osaka F-term (reference) 4C023 GA03 4C033 AB06 4C036 AD08 AD20 4C055 AA01 BA02 BA06 BA28 BA42 BA47 BB02 BB04 BB10 BB11 BB15 CA01 CA03 CA06 CA13 CA39 DA01 4H006 AA01 AA03 AB02 TA01 TA02 TA03 4H011 AC01 BA01 BA06 BB03 BB08 BB09 BB10 BB13 BB14 BB15 BB16 BB17 BC01 BC03 BC07 BC18 DD03 DA15 DA16 DA15 DA15 DA16

Claims (7)

[Claims] 1. The general formula (I) [Chemical 1] {In the formula, A¹Is C₁-C₈Alkylene group, the same or different
Also good, halogen atom, cyano group, nitro group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, hydroxy C₁-C₆Al
Kill group, C₁-C₆Alkoxy C₁-C₆Alkyl group, C₁-C₆A
Luquilcio C₁-C₆Alkyl group, C ₁-C₆Alkoxy carbo
Nyl group, phenyl group or the same or different,
Halogen atom, cyano group, nitro group, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C ₁-C
₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-
C₆Alkylamino group, which may be the same or different, di C₁-C₆
Alkylamino group or C₁-C₆Is it an alkoxycarbonyl group?
A substituted phenyl group having one or more substituents selected from
Substituted C having one or more substituents selected from₁-C₈Archi
Len group, C₃-C₈Alkenylene group, same or different
, Halogen atom, cyano group, nitro group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group, C₁-C₆Alkylthio C₁-
C₆Alkyl group, C₁-C₆Alkoxycarbonyl group, phenyl
Group or the same or different, a halogen atom,
Cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkylami
Group, which may be the same or different, di C₁-C₆Alkylamino
Group or C₁-C₆1 selected from alkoxycarbonyl groups
1 selected from substituted phenyl groups having the above substituents
Substituted C having the above substituents₃-C₈Alkenylene group, C ₃-
C₈Alkynylene groups or may be the same or different,
Rogen atom, cyano group, nitro group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Rukylsulphonyl group, C₁-C₆Alkylthio C₁-C₆Archi
Ru radical, C ₁-C₆Alkoxycarbonyl group, phenyl group or
May be the same or different, halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁
-C₆Alkylthio group, halo C ₁-C₆Alkylthio group, C₁-C
₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
One or more positions selected from substituted phenyl groups having a substituent
Substituted C having a substituent₃-C₈An alkynylene group is shown. Also before
Note C₁-C₈Alkylene group, substituted C₁-C₈Alkylene group, C₃-
C₈Alkenylene group, substituted C₃-C₈Alkenylene group, C₃-C₈ 
Alkynylene group or substituted C₃-C₈Any in the alkynylene group
The saturated carbon atom of is C₂-C_FiveC substituted with an alkylene group₃-
C₆A cycloalkane ring can also be shown, and the C₁-C₈Al
Xylene group, substituted C₁-C₈Alkylene group, C₃-C₈Alkenile
Group or substituted C₃-C₈Any two charcoal in alkenylene group
Elementary atoms together with alkylene or alkenylene groups
Te C₃-C₆Cycloalkane ring or C₃-C₆Cycloalkene ring
Can also be indicated. R¹Is a hydrogen atom, a mercapto group,
 C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C
₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalkyl group,
A phenyl group, which may be the same or different, a halogen atom,
Cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C ₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C ₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkylami
Group, which may be the same or different, di C₁-C₆Alkylamino
Group or C₁-C₆1 selected from alkoxycarbonyl groups
Substituted phenyl group having the above substituents, phenylthio
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆ Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenylthio group having a substituent, a heterocyclic group, the same or
May be different, halogen atom, cyano group, nitro group,
 C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Al
Coxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C₁-C₆Alkylsul
Finyl group, halo C₁-C₆Alkylsulfinyl group, C₁-
C₆Alkylsulfonyl group, halo C₁-C₆Alkyl sulfoni
Lu group, Mono C₁-C₆Alkylamino group, the same or different
Also good C₁-C₆Alkylamino group or C ₁-C₆Alkoxy
A device having one or more substituents selected from carbonyl groups
A heterocyclic group or -A²-R^Four(In the formula, A² Is -C (= O)
-, -C (= S)-, -C (= NR^Five)-(Wherein R^Five
Is a hydrogen atom, C₁-C₆Alkyl group, C₁-C₆An alkoxy group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group, C₁-C₆Alkoxy Carboni
Groups, phenyl groups or the same or different,
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rukylamino group, which may be the same or different, di C₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted phenyl group having one or more selected substituents
You ), C₁-C₈Alkylene group, halo C₁-C₈Alkylene
Base, C₃-C₆Alkenylene group, halo C₃-C₆Alkenylene
Base, C₃-C₆Alkynylene group or halo C₃-C₆Alkynylene
Shows the group (1) A² Is -C (= O)-, -C (= S)-or -C
(= NR^Five)-(Wherein R^FiveIs the same as above. )
If R^FourIs a hydrogen atom, C₁-C₆Alkyl group, halo C ₁-C₆A
Rukiru group, C₃-C₆Cycloalkyl group, halo C₃-C₆Cyclo
Alkyl groups, phenyl groups, which may be the same or different,
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rukylamino group, which may be the same or different, di C₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted heterocyclic group having a substituent or -Z¹-R⁶(In the formula, Z¹ 
Is -O- -S- or -N (R⁷)-(Wherein R⁷Is water
Elementary atom, C₁-C₆Alkyl group, C₁-C₆Alkyl carbonyl
Group, halo c₁-C₆Alkylcarbonyl group or C₁-C₆Arcoki
Indicates a carbonyl group. ), And R⁶Is a hydrogen atom, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C ₃-C₆Arche
Nyl group, halo C₃-C₆Alkenyl group, C₃-C₆Alkynyl
Group, halo c₃-C₆Alkynyl group, C₃-C₆Cycloalkyl
Groups, phenyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
Substituted phenyl group having one or more substituents, phenyl C₁-
C_FourAlkyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C ₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
Substituted Phenyl C Having One or More Substituents on the Ring₁-C_FourAl
Kill group, heterocyclic group, or the same or different.
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rukylamino group, which may be the same or different, di C₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted heterocyclic group having one or more selected substituents
You ) Is shown. (2) A² Is C₁-C₈Alkylene group, halo C₁-C₈Arche
Group, C₃-C₆Alkenylene group, halo C₃-C₆Alkenylene
Base, C₃-C₆Alkynylene group or halo C₃-C₆Alkynylene
When a group is shown, R^FourIs hydrogen atom, halogen atom, cyano
Group, nitro group, C ₃-C₆Cycloalkyl group, halo C₃-C₆Shi
Chloroalkyl group, C₁-C₆Alkoxycarbonyl group, mono
 C₁-C₆Alkylaminocarbonyl group, the same or different
Also good C ₁-C₆Alkylaminocarbonyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C ₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Heterocyclic group or -Z²-R⁸(In the formula, Z² Is -O-, -S-
  -SO- -SO₂-, -N (R⁹)-(Wherein R⁹Is
Hydrogen atom, C₁-C₆Alkyl group, C₁-C₆Alkyl Carboni
Lu group, halo C₁-C₆Alkylcarbonyl group, C₁-C₆Arco
Xycarbonyl group, phenylcarbonyl group or same
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group or halo C₁-C₆Alkyls
Substitution with one or more substituents selected from the group
Indicates a phenylcarbonyl group. ), -C (= O)-or
-C (= NOR^Ten)-(Wherein R^TenIs a hydrogen atom, C₁-C₆
Alkyl group, halo C₁-C₆Alkyl group, C₃-C₆Alkenyl
Group, halo c₃-C₆Alkenyl group, C₃-C₆Alkynyl group, ha
B C₃-C₆Alkynyl group, C₃-C₆Cycloalkyl group,
Nil C₁-C_FourAlkyl group or same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo C₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C ₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
A substituted phenyl having on the ring one or more substituents selected from
Nil C₁-C_FourIndicates an alkyl group. ), And R⁸Is hydrogen
Child, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₃-C₆
Alkenyl group, halo C₃-C₆Alkenyl group, C₃-C₆Archi
Nyl group, halo C₃-C₆Alkynyl group, C₃-C₆Cycloalk
Ru radical, C₁-C₆Alkylcarbonyl group, halo C₁-C₆Archi
Lecarbonyl group, C₁-C₆Alkoxycarbonyl group, mono
 C₁-C₆Alkylaminocarbonyl group, the same or different
Also good C₁-C₆Alkylaminocarbonyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁
-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C
₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted phenyl group having a substituent, phenyl C₁-C_FourAlkyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted phenyl C having a substituent on the ring₁-C_FourAlkyl group, multiple
It may be a cyclic group or the same or different and may be a halogen atom.
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C ₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C ₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
A substituted heterocyclic group having one or more substituents is shown. )
You ) Is shown. Also, R¹Is A¹Combined with one or two
Oxygen atom, sulfur atom or nitrogen source which may be the same or different
To form a 5- to 8-membered ring which may be interrupted by the child
it can. R²And R³May be the same or different, and hydrogen
Atom, C₃-C₆Cycloalkyl group or -A²-R^Four(In the formula,
A²And R^FourIs the same as above. ) Is shown. Also, R²Is A¹
Or R¹1 to 2 same or different may be combined with
Even if interrupted by oxygen, sulfur or nitrogen atoms
A good 5- to 7-membered ring can be formed. X is the same or
May be different, halogen atom, cyano group, nitro group,
 C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalkyl
Base, C₁-C₆Alkoxycarbonyl group, phenyl group, same
Or may be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group, halo C₁-C₆Alkylsul
Honyl group, Mono C₁-C₆Alkylamino group, same or different
I'm good C₁-C₆Alkylamino group or C₁-C₆Arco
Having one or more substituents selected from oxycarbonyl groups
Substituted phenyl group, heterocyclic group, same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo C₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C ₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
A substituted heterocyclic group having one or more substituents selected from
Is -A³-R¹¹(In the formula, A³ Is -O-, -S-, -SO
-, -SO₂-, -C (= O)-, -C (= NOR¹²)
-(In the formula, R¹²Is a hydrogen atom, C₁-C₆Alkyl group, halo C
₁-C₆Alkyl group, C₃-C₆Alkenyl group, halo C₃-C₆Al
Kenyl group, C₃-C₆Alkynyl group, C₃-C₆Cycloalkyl
Group, phenyl C₁-C_FourAlkyl group or same or different
May be, halogen atom, cyano group, nitro group, C₁-C₆
Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆Al
Killsulfonyl group, halo C₁-C₆An alkylsulfonyl group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group or C₁-C₆Alkoxy carbo
An arrangement having on the ring one or more substituents selected from the group nyl.
Converted phenyl C₁-C_FourIndicates an alkyl group. ), C₁-C₆Archi
Ren group, halo C₁-C₆Alkylene group, C₂-C₆Alkenylene
Group, halo c₂-C₆Alkenylene group, C₂-C₆Alkynylene group
Or halo C₃-C₆An alkynylene group, (1) A³But-
O-, -S-, -SO- or -SO₂-Indicates R
¹¹Is halo c₃-C₆Cycloalkyl group, halo C₃-C₆Cycloa
Lucenyl group, phenyl group, which may be the same or different,
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rualkylamino group, di-C which may be the same or different₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C ₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted heterocyclic group having a substituent or -A^Four-R¹³(In the formula, A^Four
Is C₁-C₆Alkylene group, halo C₁-C₆Alkylene group, C₃-
C₆Alkenylene group, halo C₃-C₆Alkenylene group, C₃-C₆
Alkynylene group or halo C₃-C₆Represents an alkynylene group,
R¹³Is hydrogen atom, halogen atom, C ₃-C₆Cycloalkyl
Group, halo c₃-C₆Cycloalkyl group, C₁-C₆Alkoxyca
Rubonyl group, phenyl group, which may be the same or different,
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C ₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rukylamino group, which may be the same or different, di C₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted phenyl group having one or more selected substituents or-
A^Five-R¹⁴(In the formula, A^FiveIs -O-, -S-, -SO-,-
SO₂-Or-C (= O) -indicates R¹⁴Is C₁-C₆Al
Kill group, halo C₁-C₆Alkyl group, C₃-C₆An alkenyl group,
Halo c₃-C₆Alkenyl group, C₃-C₆Alkynyl group, halo C
₃-C₆Alkynyl group, C₃-C₆Cycloalkyl group, halo C₃-
C₆Cycloalkyl group, phenyl group, the same or different
Well, halogen atom, cyano group, nitro group, C₁-C₆Al
Kill group, halo C₁-C₆Alkyl group, C₁-C₆An alkoxy group,
Halo c₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo
 C₁-C₆Alkylthio group, C₁-C₆Alkylsulfinyl
Group, halo c₁-C₆Alkylsulfinyl group, C₁-C₆Archi
Lesulfonyl group, halo C₁-C₆Alkylsulfonyl group,
No C₁-C₆An alkylamino group, which may be the same or different
 C₁-C₆Alkylamino group or C₁-C₆Alkoxy Carboni
Substituted phenyl having one or more substituents selected from
Group, heterocyclic group or the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Is a substituted heterocyclic group having one or more substituents. )
Indicates (2) A³ Is -C (= O)-or -C (= NO
R¹²)-(Wherein R¹²Is the same as above. ) Indicates R
¹¹Is a hydrogen atom, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₂-C₆Alkenyl group, halo C₂-C₆Alkenyl group, C
₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalkyl group,
 C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, Mono C₁-C
₆Alkylamino group, which may be the same or different, di C₁-C₆
Alkylamino group, phenyl group, same or different
, Halogen atom, cyano group, nitro group, C ₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
Substituted phenyl having one or more substituents selected from
Groups, phenylamino groups, which may be the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Substituted Phenylamido Having One or More Substituents on the Ring
Group, a heterocyclic group, or the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Killamino group, di-C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted heterocyclic group having one or more substituents,
(3) A³ Is C₁-C₆Alkylene group, halo C₁-C₆Arche
Group, C₂-C₆Alkenylene group, halo C₂-C₆Alkenylene
Base, C₂-C₆Alkynylene group or halo C₃-C₆Alkynylene
When a group is shown, R¹¹Is a hydrogen atom, hydroxy group, halogen
Atom, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloa
Rukiru group, C₁-C₆Alkoxycarbonyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C ₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Heterocyclic group or -A⁶-R¹⁵(In the formula, A⁶ Is -O-, -S
-, -SO- or -SO₂-Indicates R¹⁵Is C₃-C₆Shiku
Lower alkyl group, halo C₃-C₆Cycloalkyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Heterocyclic group or -A⁷-R¹⁶(In the formula, A⁷ Is C ₁-C₆Arche
Group, halo C₁-C₆Alkylene group, C₂-C₆Alkenylene
Group, halo c₂-C₆Alkenylene group, C₂-C₆Alkynylene group
Or halo C₃-C₆Represents an alkynylene group, R¹⁶Is hydrogen
Child, halogen atom, C₃-C₆Cycloalkyl group, halo C₃-
C₆Cycloalkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, phenyl group,
One or different, halogen atom, cyano group, nit
B, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-
C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Al
Kirthio group, halo C₁-C₆Alkylthio group, C ₁-C₆Archi
Rusulfinyl group, halo C₁-C₆Alkylsulfinyl
Base, C₁-C₆Alkylsulfonyl group, halo C₁-C₆Alkyl
Sulfonyl group, mono C₁-C₆Alkylamino group, same or
It may be different C₁-C₆Alkylamino group or C₁-C₆A
One or more substituents selected from lucoxycarbonyl groups
Having a substituted phenyl group, a phenoxy group, the same or different
May be, halogen atom, cyano group, nitro group, C₁-C₆
Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆Al
Killsulfonyl group, halo C₁-C₆An alkylsulfonyl group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group or C₁-C₆Alkoxy carbo
Substituted Fe having one or more substituents selected from the group
A nonoxy group, a phenylthio group, which may be the same or different,
Halogen atom, cyano group, nitro group, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C
₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-
C₆Alkylamino group, which may be the same or different, di C ₁-C₆
Alkylamino group or C₁-C₆Is it an alkoxycarbonyl group?
Substituted phenylthio having one or more substituents selected from
Groups, heterocyclic groups or the same or different, halogen
Atom, cyano group, nitro group, C₁-C₆Alkyl group, halo
 C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆A
Lucoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Archi
Ruthio group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆
Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Is a heterocyclic group having one or more substituents. )
You ) Is shown and l shows the integer of 0-4. Also, X is
A fused ring together with adjacent carbon atoms on the nyl ring
Can be formed and the fused rings can be the same or different.
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁
-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
It can also have one or more substituents selected from
Y may be the same or different, and a halogen atom, cyano
Group, nitro group, halo C₃-C₆A cycloalkyl group, the same or
May be different C₁-C₆Alkylsilyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Heterocyclic group or -A³-R¹¹(In the formula, A³ And R¹¹Is above
the same. ) Is shown and m shows the integer of 0-5. Also, Y is
Fused ring with adjacent carbon atoms on the phenyl ring
And the fused rings may be the same or different.
Well, halogen atom, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
C₁-C₆Alkylsulfonyl group, phenyl group, same or different
Can be halogen atom, cyano group, nitro group, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arco
Xy, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C ₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Phenyl group, heterocyclic group or same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C ₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
A substituted heterocyclic group having one or more substituents selected from
It can also have one or more substituents selected from n
Represents an integer of 0 to 2. However, X, R²And R³At the same time
Is a hydrogen atom, m is an integer of 2, and Y is a 2-position.
When a fluorine atom is shown and the 3-position is a chlorine atom, A¹Is
Ropylene group, R¹Is a methyl group and n is 0
Except when showing numbers. Further, the lid represented by the general formula (I)
The amide derivative is N²-(1,1-dimethyl-2-methyl
Thioethyl) -3-iodo-N¹-{2-methyl-4-
[1,2,2,2-tetrafluoro-1- (trifluoro
(Methyl) ethyl] phenyl} phthalamide, N²−
(1,1-dimethyl-2-methylsulfonylethyl)-
3-Iodo-N¹-{2-methyl-4- [1,2,2,2
2-tetrafluoro-1- (trifluoromethyl) eth
Lu] phenyl} phthalamide or N²-(1,1-Jime
Cyl-2-methylsulfinylethyl) -3-iodo-
N¹-{2-methyl-4- [1,2,2,2-tetraf
Luoro-1- (trifluoromethyl) ethyl] pheny
Ru} phthalamide is excluded. } Lid represented by
A amide derivative or a salt thereof. 2. A¹Is C₁-C₈Alkylene group, same or different
Halogen atom, halo C₁-C₆An alkyl group,
 C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group, halo C₁-C₆Archi
Lesulfonyl group, C₁-C₆Alkylthio C₁-C₆Alkyl
Groups, phenyl groups or may be the same or different, halo
Gen atom, C₁-C₆Alkyl group, halo C₁-C₆An alkyl group,
 C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Al
Having one or more substituents selected from a sulfonyl group
Have one or more substituents selected from substituted phenyl groups
Substitution C₁-C₈Alkylene group, C₃-C₈Alkenylene group,
May be one or different, halogen atom, halo C₁-C₆Al
Kill group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group or C ₁-C₆Alkylthio C
₁-C₆Having one or more substituents selected from alkyl groups
Substitution C₃-C₈Alkenylene group, C₃-C₈ Alkynylene group or
May be the same or different, halogen atom, halo C₁-C
₆ Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group or C₁-C₆Alkylthio
 C₁-C₆Have one or more substituents selected from alkyl groups
Substitution C₃-C₈An alkynylene group,₁-C₈Archi
Ren group, substituted C₁-C₈Alkylene group, C₃-C₈Alkenylene
Group, substituted C₃-C₈Alkenylene group, C₃-C₈ Alkynylene group
Or substitution C₃-C₈Any saturated carbon atom in the alkynylene group
Is C₂-C_FiveC substituted with an alkylene group₃-C₆Cycloalca
Can also be represented by the C₁-C₈Alkylene group, substituted
 C₁-C₈Alkylene group, C₃-C₈Alkenylene group, substituted C₃-
C₈Any two carbon atoms in the alkenylene group are alkyle
C together with benzene or alkenylene groups₃-C₆Cycloa
Lucan ring or C₃-C₆Can also represent a cycloalkene ring
It R¹Is a hydrogen atom, mercapto group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C₃-C₆Cycloalk
Lu group, halo C₃-C₆Cycloalkyl group, phenyl group, same
Or may be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C ₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group, halo C ₁-C₆Alkylsul
Honyl group, Mono C₁-C₆Alkylamino group, same or different
I'm good C₁-C₆Alkylamino group or C₁-C₆Arco
Having one or more substituents selected from oxycarbonyl groups
Substituted phenyl group, phenylthio group, the same or different
Also good, halogen atom, cyano group, nitro group, C₁-C₆A
Rukiru group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆Al
Killsulfonyl group, halo C₁-C₆An alkylsulfonyl group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group or C₁-C₆Alkoxy carbo
Substituted Fe having one or more substituents selected from the group
Nylthio group, heterocyclic group, which may be the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C ₁-C₆Select from alkoxycarbonyl groups
Substituted heterocyclic group having one or more substituents or -A²-
R^Four(In the formula, A² Is -C (= O)-, -C (= S)-,
-C (= NR^Five)-(Wherein R^FiveIs a hydrogen atom, C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Noki, C₁-C₆Alkoxycarbonyl group, phenyl group or
May be the same or different, halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
The substituted phenyl group is shown. ), C₁-C₈Alkylene
Group, halo c₁-C₈Alkylene group, C₃-C₆Alkenylene group,
Halo c₃-C₆Alkenylene group, C₃-C₆Alkynylene group or
Halo c₃-C₆An alkynylene group, (1) A² Is -C
(= O)-, -C (= S)-or -C (= NR^Five) −
(In the formula, R^FiveIs the same as above. ) Indicates R^FourIs hydrogen
Atom, C₁-C₆Alkyl group, halo C ₁-C₆Alkyl group, C₃-
C₆Cycloalkyl group, halo C₃-C₆Cycloalkyl group,
Phenyl group, which may be the same or different, a halogen atom,
Ano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Al
Kill group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Can be halogen atom, cyano group, nitro group, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arco
Xy, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C ₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆ 
Alkylsulfonyl group or halo C₁-C₆Alkyl sulfoni
Substituted heterocycle having one or more substituents selected from the group
Group or -Z¹-R⁶(In the formula, Z¹ Is -O-, -S- or-
N (R⁷)-(Wherein R⁷Is a hydrogen atom, C₁-C₆Alkyl
Base, C₁-C₆Alkylcarbonyl group, halo C₁-C₆Alkyl
Carbonyl group or C₁-C₆Indicates an alkoxycarbonyl group
You ), And R⁶Is a hydrogen atom, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₃-C₆Alkenyl group, halo C₃-C₆
Alkenyl group, C₃-C₆Alkynyl group, halo C₃-C₆Archi
Nyl group, C₃-C₆Cycloalkyl group, phenyl group, same or
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
C₁-C₆ Alkylsulfonyl group or halo C₁-C₆Alkyls
Substitution with one or more substituents selected from the group
Phenyl group, Phenyl C ₁-C_FourAlkyl group, same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group or halo C₁-C₆Alkyl sulfoni
Substituted with one or more substituents selected from
Phenyl C₁-C_FourAlkyl group, heterocyclic group or the same or
May be different, halogen atom, cyano group, nitro group,
 C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Al
Coxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C₁-C₆Alkylsul
Finyl group, halo C₁-C₆Alkylsulfinyl group, C₁-
C₆Alkylsulfonyl group or halo C₁-C₆Alkyl sulfo
Substituted heterocycle having one or more substituents selected from nyl group
Indicates a ring group. ), And (2) A² Is C₁-C₈Alkylene
Group, halo c₁-C₈Alkylene group, C₃-C₆Alkenylene group,
Halo c₃-C₆Alkenylene group, C₃-C₆Alkynylene group or
Halo c₃-C₆When an alkynylene group is shown, R^FourIs hydrogen
Child, halogen atom, cyano group, nitro group, C ₃-C₆Cyclo
Alkyl group, halo C₃-C₆Cycloalkyl group, C₁-C₆Al
Coxycarbonyl group, mono C₁-C₆Alkylaminocarbo
Nyl group, which may be the same or different, di C ₁-C₆Alkylami
Nocarbonyl group, phenyl group, the same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C ₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Rufonyl group or halo C₁-C₆Select from alkylsulfonyl group
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
A substituted heterocyclic group having -Z²-R⁸(In the formula, Z² Is -O
-, -S- -SO- -SO₂-, -N (R⁹)-(Expression
Medium, R⁹Is a hydrogen atom, C₁-C₆Alkyl group, C₁-C₆Archi
Lucarbonyl group, halo C ₁-C₆Alkylcarbonyl group, C
₁-C₆Alkoxycarbonyl group, phenylcarbonyl group or
May be the same or different, and may be a halogen atom, cyano
Group, nitro group, C ₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
The substituted phenylcarbonyl group is shown. ), -C (=
O)-or -C (= NOR^Ten-(In the formula, R^TenIs hydrogen
Child, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₃-C₆
Alkenyl group, halo C₃-C₆Alkenyl group, C₃-C₆Archi
Nyl group, halo C₃-C₆Alkynyl group, C₃-C₆Cycloalk
Group, phenyl C₁-C_FourAlkyl group or same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group or halo C₁-C₆Alkyl sulfoni
Substituted with one or more substituents selected from
Phenyl C₁-C_FourIndicates an alkyl group. ), And R⁸Is water
Elementary atom, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₃-C₆Alkenyl group, halo C₃-C₆Alkenyl group, C₃-C₆A
Lucinyl group, halo C₃-C₆Alkynyl group, C₃-C₆Cycloa
Rukiru group, C₁-C₆Alkylcarbonyl group, halo C₁-C₆A
Rukylcarbonyl group, C₁-C₆An alkoxycarbonyl group,
Mono C₁-C₆Alkylaminocarbonyl group, same or different
I'm good C₁-C₆Alkylaminocarbonyl group,
Nyl group, which may be the same or different, may be a halogen atom or a sialic group.
No group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Archi
Ru radical, C₁-C₆Alkoxy group, halo C₁-C₆An alkoxy group,
 C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C
₁-C₆Alkylsulfinyl group, halo C₁-C₆Alkylsul
Finyl group, C₁-C₆Alkylsulfonyl group or halo C₁-
C₆One or more substituents selected from alkylsulfonyl groups
A substituted phenyl group having phenyl C₁-C_FourAn alkyl group,
They may be the same or different and may be a halogen atom, a cyano group, or
Toro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆A
Rukiruthio group, halo C₁-C₆Alkylthio group, C₁-C₆Al
Kirsulfinyl group, halo C₁-C₆Alkylsulfinyl
Base, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Archi
On the ring one or more substituents selected from
Substituted phenyl C having₁-C_FourAlkyl group, heterocyclic group or the same
One or different, a halogen atom, a cyano group,
Nitro group, C₁-C₆Alkyl group, halo C₁-C₆An alkyl group,
 C ₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Al
Having one or more substituents selected from a sulfonyl group
Represents a substituted heterocyclic group. ) Is shown. ) Is shown. Also, R¹
Is A¹1 or 2 may be the same or different by combining with
It may be interrupted by oxygen, sulfur or nitrogen atoms.
A 5- to 8-membered ring can be formed. R²And R³Is
May be the same or different, hydrogen atom, C₃-C₆ Cycloal
Kill group or -A²-R^Four(In the formula, A²And R^FourIs the same as above
Same. ) Is shown. Also, R²Is A¹Or R¹Combined with 1
Up to two identical or different oxygen atoms, sulfur atoms or
Form a 5-7 membered ring which may be interrupted by a nitrogen atom
You can X may be the same or different, and
Atom, cyano group, nitro group, C₁-C₆Alkyl group, halo
 C₁-C₆Alkyl group, C₂-C₆Alkenyl group, halo C₂-C₆A
Lucenyl group, C₂-C₆Alkynyl group, halo C₂-C₆Alkini
Ru radical, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloal
Kill group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, C₁-
C₆Alkylsulfonyl group or C₁-C₆Alkoxy Carboni
Group, and l represents an integer of 0 to 4. Also, X is pheny
Form a fused ring with adjacent carbon atoms on the ring.
The condensed rings may be the same or different.
Black, halogen atom, C₁-C₆Alkyl group, halo C₁-C₆Al
Kill group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
It can also have a substituent. Y may be the same or different
Well, halogen atom, cyano group, nitro group, halo C₃-C₆
A cycloalkyl group, which may be the same or different, tri C₁-C₆
Alkylsilyl group, phenyl group, same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Rufonyl group or halo C₁-C₆Select from alkylsulfonyl group
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C
₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
A substituted heterocyclic group having -A³-R¹¹(In the formula, A³ Is -O
-, -S-, -SO-, -SO₂-, -C (= O)-,-
C (= NOR¹²)-(Wherein R¹²Is a hydrogen atom, C₁-C₆A
Rukiru group, halo C₁-C₆Alkyl group, C₃-C₆Alkenyl
Group, halo c₃-C₆Alkenyl group, C₃-C₆Alkynyl group, C₃
-C₆Cycloalkyl group, phenyl C₁-C_FourAlkyl group or the same
One or different, a halogen atom, a cyano group,
Nitro group, C₁-C₆Alkyl group, halo C₁-C₆An alkyl group,
 C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C ₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Al
Having one or more substituents selected from a sulfonyl group
Phenyl C₁-C_FourIndicates an alkyl group. ), C₁-C₆Archi
Ren group, halo C₁-C₆Alkylene group, C₂-C₆Alkenylene
Group, halo c₂-C₆Alkenylene group, C ₂-C₆Alkynylene group
Or halo C₃-C₆An alkynylene group, (1) A³But-
O-, -S-, -SO- or -SO₂-Indicates R
¹¹Is a phenyl group, which may be the same or different and may be a halogen source.
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group or
Halo c₁-C₆One or more selected from alkylsulfonyl groups
A substituted phenyl group having a substituent of, a heterocyclic group, the same or
May be different, halogen atom, cyano group, nitro group,
 C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Al
Coxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C ₁-C₆Alkylsul
Finyl group, halo C₁-C₆Alkylsulfinyl group, C₁-
C₆Alkylsulfonyl group or halo C₁-C₆Alkyl sulfo
Substituted heterocycle having one or more substituents selected from nyl group
Ring group or -A^Four-R¹³(In the formula, A^FourIs C₁-C₆Alkylene
Group, halo c₁-C₆Alkylene group, C₃-C₆Alkenylene group,
Halo c₃-C₆Alkenylene group, C₃-C₆Alkynylene group or
Halo c₃-C₆Represents an alkynylene group, R¹³Is a hydrogen atom,
Rogen atom, C₃-C₆Cycloalkyl group, halo C₃-C₆Shiku
Alkyl group, phenyl group, may be the same or different,
Halogen atom, cyano group, nitro group, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
 C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-
C₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group or halo C₁-C₆Select from alkylsulfonyl groups
Substituted phenyl group having one or more substituents or -A
^Five-R¹⁴(In the formula, A^FiveIs -O-, -S-, -SO-, -S
O ₂-Or-C (= O) -indicates R¹⁴Is C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₃-C₆Alkenyl group, ha
B C₃-C₆Alkenyl group, C₃-C₆Alkynyl group, halo C₃-C
₆Alkynyl group, C₃-C₆Cycloalkyl group, halo C₃-C₆
Cycloalkyl group, phenyl group, same or different
, Halogen atom, cyano group, nitro group, C ₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Rufonyl group or halo C₁-C₆Select from alkylsulfonyl group
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups or the same or different, a halogen atom,
Cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
A substituted heterocyclic group having a substituent is shown. ), And (2)
A³ Is -C (= O)-or -C (= NOR¹²) (Where
R¹²Is the same as above. ) Indicates R¹¹Is a hydrogen atom, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₂-C₆Arche
Nyl group, halo C₂-C₆Alkenyl group, C₃-C₆Cycloalk
Lu group, halo C₃-C₆Cycloalkyl group, C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, Mono C ₁-C₆Alkylamino
Groups, which may be the same or different, di C₁-C₆Alkylamino
Groups, phenyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group or
Halo c₁-C₆One or more selected from alkylsulfonyl groups
A substituted phenyl group having a substituent of, a phenylamino group,
They may be the same or different and may be a halogen atom, a cyano group, or
Toro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆A
Rukiruthio group, halo C₁-C₆Alkylthio group, C₁-C₆Al
Kirsulfinyl group, halo C₁-C₆Alkylsulfinyl
Base, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Archi
On the ring one or more substituents selected from
Having a substituted phenylamino group, a heterocyclic group or the same or younger
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group or halo C₁-C₆Alkyls
Substitution with one or more substituents selected from the group
Represents a heterocyclic group, (3) A³ Is C₁-C₆Alkylene group, ha
B C₁-C₆Alkylene group, C₂-C₆Alkenylene group, halo C
₂-C₆Alkenylene group, C₂-C₆Alkynylene group or halo C
₃-C₆When an alkynylene group is shown, R¹¹Is a hydrogen atom, hydr
Roxy group, halogen atom, C₃-C₆Cycloalkyl group, ha
B C₃-C₆Cycloalkyl group, C₁-C₆Alkoxy Carboni
Group, phenyl group, same or different, halogen
Atom, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁
-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Al
Coxy group, C₁-C₆Alkylthio group, halo C₁-C₆Alkyl
Thio group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆A
Rukylsulfinyl group, C₁-C₆Alkylsulfonyl group
Is halo c₁-C₆1 or more selected from alkylsulfonyl groups
A substituted phenyl group having the above substituent, a heterocyclic group, the same or
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group or halo C₁-C₆Alkyls
Substitution with one or more substituents selected from the group
Heterocyclic group or -A⁶-R¹⁵(In the formula, A⁶ Is -O-, -S
-, -SO- or -SO₂-Indicates R¹⁵Is C₃-C₆Shiku
Lower alkyl group, halo C₃-C₆Cycloalkyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C ₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
Having a substituted phenyl group, a heterocyclic group, the same or different
Well, halogen atom, cyano group, nitro group, C₁-C₆Al
Kill group, halo C₁-C₆Alkyl group, C₁-C₆An alkoxy group,
Halo c₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo
C₁-C₆Alkylthio group, C₁-C₆Alkylsulfinyl
Group, halo c₁-C₆Alkylsulfinyl group, C₁-C₆Archi
Sulfonyl group or halo C₁-C₆Alkylsulfonyl group
A substituted heterocyclic group having one or more substituents selected from
-A⁷-R¹⁶(In the formula, A⁷ Is C₁-C₆Alkylene group, halo C
₁-C₆Alkylene group, C₂-C₆Alkenylene group, halo C₂-C₆
Alkenylene group, C₂-C₆Alkynylene group or halo C₃-C₆
Represents an alkynylene group, R¹⁶Is hydrogen atom, halogen atom
Child, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalk
Ru radical, C₁-C₆Alkoxy group, halo C₁-C₆An alkoxy group,
 C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C
₁-C₆Alkylsulfinyl group, halo C₁-C₆Alkylsul
Finyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆
Alkylsulfonyl group, phenyl group, the same or different
Also good, halogen atom, cyano group, nitro group, C₁-C₆A
Rukiru group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C ₁-C₆Al
Killsulfonyl group or halo C₁-C₆Alkylsulfonyl group
Substituted phenyl having one or more substituents selected from
Groups, phenoxy groups, which may be the same or different, halogen
Atom, cyano group, nitro group, C₁-C₆Alkyl group, halo C
₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Al
Coxy group, C₁-C₆Alkylthio group, halo C₁-C₆Alkyl
Thio group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆A
Rukylsulfinyl group, C₁-C₆Alkylsulfonyl group
Is halo c₁-C₆1 or more selected from alkylsulfonyl groups
Substituted phenoxy group having the above substituent, phenylthio
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
Having a substituted phenylthio group, a heterocyclic group or the same or
May be different, halogen atom, cyano group, nitro group,
 C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Al
Coxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C₁-C₆Alkylsul
Finyl group, halo C₁-C₆Alkylsulfinyl group, C₁-
C₆Alkylsulfonyl group or halo C₁-C₆Alkyl sulfo
Heterocyclic group having one or more substituents selected from nyl group
Indicates. ) Is shown. ), M is an integer of 1 to 5
You Also, Y is the same as the adjacent carbon atom on the phenyl ring.
To form a condensed ring, and the condensed rings are the same.
Or may be different, halogen atom, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
 C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C
₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group or halo C₁-C₆Select from alkylsulfonyl groups
Can have one or more substituents, and n is 0 to 2
Or a phthalamide derivative according to claim 1, which represents an integer of
salts. 3. A¹Is C₁-C₈Alkylene group, same or different
Halogen atom, halo C₁-C₆An alkyl group,
 C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group, halo C₁-C₆Archi
Lesulfonyl group or C₁-C₆Alkylthio C₁-C₆Alkyl
Substituted C having one or more substituents selected from the group₁-C₈A
Represents a alkylene group, and₁-C₈Alkylene group or substituted C
₁-C₈Any saturated carbon atom in the alkylene group is C₂-C_FiveAl
C substituted with a xylene group₃-C₆Indicates a cycloalkane ring
You can also do the above C₁-C₈Alkylene group or C₁-C₈Arche
Any two carbon atoms in the phenyl group together with the alkylene group
Become C₃-C₆It can also represent a cycloalkane ring. R
¹Is a hydrogen atom, mercapto group, C₁-C₆Alkyl group, halo
 C₁-C₆Alkyl group, C₃-C₆Alkenyl group, halo C₃-C₆A
Lucenyl group, C₃-C₆Alkynyl group, halo C₃-C₆Alkini
Ru radical, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloal
Kill group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkoxy C₁-C₆Alkyl group, C₁-C₆Al
Kircio C₁-C₆Alkyl group, Mono C₁-C₆Alkylamino
 C₁-C₆Alkyl groups, which may be the same or different, di C₁-C₆A
Rukiruamino C₁-C₆Alkyl group, C₁-C₆Alkyl carbo
Nyl group, halo C₁-C₆Alkylcarbonyl group, C₁-C₆Al
Kirthiocarbonyl group, C₁-C₆Alkoxy carbonyl
Group, Mono C₁-C₆Alkylaminocarbonyl group, the same or
It may be different C₁-C₆An alkylaminocarbonyl group,
Mono C₁-C₆Alkylaminothiocarbonyl group, the same or
It may be different C ₁-C₆Alkylaminothiocarbonyl
Base, C₁-C₆Alkylcarbonyl C₁-C₆Alkyl group, C₁-
C₆Alkoxyimino C₁-C₆Alkyl group, C₁-C₆Arcoki
Sicarbonyl C₁-C₆Alkyl group, Mono C₁-C₆Alkyla
Minocarbonyl C₁-C₆Alkyl groups, whether identical or different
Good the C₁-C₆Alkylaminocarbonyl C₁-C₆Alkyl
Groups, phenyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
Substituted phenyl group having one or more substituents, phenyl C₁-
C₆Alkyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
Substituted Phenyl C Having One or More Substituents on the Ring₁-C₆Al
Kill group, phenylcarbonyl group, same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
Substituted phenyl group having one or more substituents selected from
Rubonyl group, phenylthio group, same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
A substituted phenyl group having one or more substituents selected from
An o group, a heterocyclic group, or the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Is a substituted heterocyclic group having one or more substituents.
Also, R¹Is A¹Combined with 1 or 2 identical or different
May be interrupted by an oxygen atom, sulfur atom or nitrogen atom.
It may form a 5- to 8-membered ring which may be present. R²Over
And R³May be the same or different, and may be a hydrogen atom or C₁-C₆
Indicates an alkyl group. Also, R²Is A¹Or R¹Combined with
And 1 or 2 oxygen atoms which may be the same or different, sulfur
A 5-7 membered ring which may be interrupted by atoms or nitrogen atoms
Can be formed. X may be the same or different,
Halogen atom, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₂-C₆Alkenyl group, halo C₂-C₆Arche
Nyl group, C₂-C₆Alkynyl group, halo C₂-C₆Alkynyl
Base, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalk
Ru radical, C₁-C₆Alkoxy group, halo C₁-C₆An alkoxy group,
 C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C
₁-C₆Alkylsulfinyl group, halo C₁-C₆Alkylsul
Finyl group, C₁-C₆Alkylsulfonyl group or halo C₁-
C₆Represents an alkylsulfonyl group, and l represents an integer of 0 to 4
You Also, X is the same as the adjacent carbon atom on the phenyl ring.
To form a condensed ring, and the condensed rings are the same.
Or may be different, halogen atom, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
 C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C
₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group or halo C₁-C₆Select from alkylsulfonyl groups
It may also have one or more substituents as defined. Y is the same
Or may be different, halogen atom, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, hydroxyhalo C₁-C₆Al
Kill group, C₁-C₆Alkoxy halo C₁-C₆Alkyl group, C₁-
C₆Alkylthiohalo C₁-C₆Alkyl group, C₃-C₆Archeni
Lu group, halo C₃-C₆Alkenyl group, C₃-C₆An alkynyl group,
Halo c₃-C₆Alkynyl group, C₁-C₆Alkoxy group, halo C
₁-C₆Alkoxy group, C₁-C₆Alkoxy halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthiohalo C₁-C₆An alkoxy group,
Halo c₁-C₆Alkoxy halo C₁-C₆Alkoxy group, halo C₃
-C₆Alkenyloxy group, C₁-C₆Alkylthio group, halo
C₁-C₆Alkylthio group, halo C₁-C₆Alkoxy halo C₁-C
₆Alkylthio group, halo C₁-C₆Alkenylthio group, C₁-C
₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group, C₁-
C₆Alkoxycarbonyl group, C₃-C₆Cycloalkyl group,
Halo c ₃-C₆Cycloalkyl group, phenyl group, same or different
Can be a halogen atom, C₁-C₆Alkyl group, halo
C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆A
Lucoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylsulfinyl group or halo
 C₁-C₆One or more positions selected from alkylsulfonyl groups
A substituted phenyl group having a substituent, a phenoxy group, the same or
May be different, halogen atom, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, halo C₁-C₆Alkylsulfinyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
A substituted phenoxy group having a substituent, a phenylthio group,
May be one or different, halogen atom, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C ₁-C
₆Alkylthio group, halo C₁-C₆Alkylsulfinyl group
Or halo C₁-C₆1 selected from alkylsulfonyl groups
Substituted phenylthio group having the above substituents, pyridylo
A xy group, which may be the same or different, a halogen atom, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, halo C₁-C₆Alkyls
Rufinyl group or halo C₁-C₆From an alkylsulfonyl group
Substituted Pyridyloxy Having One or More Substituents Selected
Groups, pyridylthio groups, which may be the same or different,
Atom, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆A
Rukiruthio group, halo C₁-C₆Alkylthio group, halo C₁-C₆
Alkylsulfinyl group or halo C₁-C₆Alkyl sulfo
A substituted pyri having one or more substituents selected from the group nyl.
Represents a dilthio group, and m represents an integer of 1 to 5. Also, Y is
Fused together with adjacent carbon atoms on the phenyl ring
Can form a ring and the fused rings can be the same or different.
Also good, halogen atom, C₁-C₆Alkyl group, halo C₁-C₆
Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arcoki
Shi group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
It may have a substituent, and n is an integer representing an integer of 0 to 2.
The phthalamide derivative or the salt thereof according to claim 2. 4. The general formula (I) [Chemical 2] {In the formula, A¹Is C₁-C₈Alkylene group, the same or different
Also good, halogen atom, cyano group, nitro group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, hydroxy C₁-C₆Al
Kill group, C₁-C₆Alkoxy C₁-C₆Alkyl group, C₁-C₆A
Luquilcio C₁-C₆Alkyl group, C ₁-C₆Alkoxy carbo
Nyl group, phenyl group or the same or different,
Halogen atom, cyano group, nitro group, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C ₁-C
₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-
C₆Alkylamino group, which may be the same or different, di C₁-C₆
Alkylamino group or C₁-C₆Is it an alkoxycarbonyl group?
A substituted phenyl group having one or more substituents selected from
Substituted C having one or more substituents selected from₁-C₈Archi
Len group, C₃-C₈Alkenylene group, same or different
, Halogen atom, cyano group, nitro group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group, C₁-C₆Alkylthio C₁-
C₆Alkyl group, C₁-C₆Alkoxycarbonyl group, phenyl
Group or the same or different, a halogen atom,
Cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkylami
Group, which may be the same or different, di C₁-C₆Alkylamino
Group or C₁-C₆1 selected from alkoxycarbonyl groups
1 selected from substituted phenyl groups having the above substituents
Substituted C having the above substituents₃-C₈Alkenylene group, C ₃-
C₈Alkynylene groups or may be the same or different,
Rogen atom, cyano group, nitro group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Rukylsulphonyl group, C₁-C₆Alkylthio C₁-C₆Archi
Ru radical, C ₁-C₆Alkoxycarbonyl group, phenyl group or
May be the same or different, halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁
-C₆Alkylthio group, halo C ₁-C₆Alkylthio group, C₁-C
₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
One or more positions selected from substituted phenyl groups having a substituent
Substituted C having a substituent₃-C₈An alkynylene group is shown. Also before
Note C₁-C₈Alkylene group, substituted C₁-C₈Alkylene group, C₃-
C₈Alkenylene group, substituted C₃-C₈Alkenylene group, C₃-C₈ 
Alkynylene group or substituted C₃-C₈Any in the alkynylene group
The saturated carbon atom of is C₂-C_FiveC substituted with an alkylene group₃-
C₆A cycloalkane ring can also be shown, and the C₁-C₈Al
Xylene group, substituted C₁-C₈Alkylene group, C₃-C₈Alkenile
Group or substituted C₃-C₈Any two charcoal in alkenylene group
Elementary atoms together with alkylene or alkenylene groups
Te C₃-C₆Cycloalkane ring or C₃-C₆Cycloalkene ring
Can also be indicated. R¹Is a hydrogen atom, a mercapto group,
 C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C
₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalkyl group,
A phenyl group, which may be the same or different, a halogen atom,
Cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C ₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C ₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkylami
Group, which may be the same or different, di C₁-C₆Alkylamino
Group or C₁-C₆1 selected from alkoxycarbonyl groups
Substituted phenyl group having the above substituents, phenylthio
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆ Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenylthio group having a substituent, a heterocyclic group, the same or
May be different, halogen atom, cyano group, nitro group,
 C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Al
Coxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C₁-C₆Alkylsul
Finyl group, halo C₁-C₆Alkylsulfinyl group, C₁-
C₆Alkylsulfonyl group, halo C₁-C₆Alkyl sulfoni
Lu group, Mono C₁-C₆Alkylamino group, the same or different
Also good C₁-C₆Alkylamino group or C ₁-C₆Alkoxy
A device having one or more substituents selected from carbonyl groups
A heterocyclic group or -A²-R^Four(In the formula, A² Is -C (= O)
-, -C (= S)-, -C (= NR^Five)-(Wherein R^Five
Is a hydrogen atom, C₁-C₆Alkyl group, C₁-C₆An alkoxy group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group, C₁-C₆Alkoxy Carboni
Groups, phenyl groups or the same or different,
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rukylamino group, which may be the same or different, di C₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted phenyl group having one or more selected substituents
You ), C₁-C₈Alkylene group, halo C₁-C₈Alkylene
Base, C₃-C₆Alkenylene group, halo C₃-C₆Alkenylene
Base, C₃-C₆Alkynylene group or halo C₃-C₆Alkynylene
Shows the group (1) A² Is -C (= O)-, -C (= S)-or -C
(= NR^Five)-(Wherein R^FiveIs the same as above. )
If R^FourIs a hydrogen atom, C₁-C₆Alkyl group, halo C ₁-C₆A
Rukiru group, C₃-C₆Cycloalkyl group, halo C₃-C₆Cyclo
Alkyl groups, phenyl groups, which may be the same or different,
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rukylamino group, which may be the same or different, di C₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted heterocyclic group having a substituent or -Z¹-R⁶(In the formula, Z¹ 
Is -O- -S- or -N (R⁷)-(Wherein R⁷Is water
Elementary atom, C₁-C₆Alkyl group, C₁-C₆Alkyl carbonyl
Group, halo c₁-C₆Alkylcarbonyl group or C₁-C₆Arcoki
Indicates a carbonyl group. ), And R⁶Is a hydrogen atom, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C ₃-C₆Arche
Nyl group, halo C₃-C₆Alkenyl group, C₃-C₆Alkynyl
Group, halo c₃-C₆Alkynyl group, C₃-C₆Cycloalkyl
Groups, phenyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
Substituted phenyl group having one or more substituents, phenyl C₁-
C_FourAlkyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C ₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
Substituted Phenyl C Having One or More Substituents on the Ring₁-C_FourAl
Kill group, heterocyclic group, or the same or different.
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rukylamino group, which may be the same or different, di C₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted heterocyclic group having one or more selected substituents
You ) Is shown. (2) A² Is C₁-C₈Alkylene group, halo C₁-C₈Arche
Group, C₃-C₆Alkenylene group, halo C₃-C₆Alkenylene
Base, C₃-C₆Alkynylene group or halo C₃-C₆Alkynylene
When a group is shown, R^FourIs hydrogen atom, halogen atom, cyano
Group, nitro group, C ₃-C₆Cycloalkyl group, halo C₃-C₆Shi
Chloroalkyl group, C₁-C₆Alkoxycarbonyl group, mono
 C₁-C₆Alkylaminocarbonyl group, the same or different
Also good C ₁-C₆Alkylaminocarbonyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C ₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Heterocyclic group or -Z²-R⁸(In the formula, Z² Is -O-, -S-
  -SO- -SO₂-, -N (R⁹)-(Wherein R⁹Is
Hydrogen atom, C₁-C₆Alkyl group, C₁-C₆Alkyl Carboni
Lu group, halo C₁-C₆Alkylcarbonyl group, C₁-C₆Arco
Xycarbonyl group, phenylcarbonyl group or same
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group or halo C₁-C₆Alkyls
Substitution with one or more substituents selected from the group
Indicates a phenylcarbonyl group. ), -C (= O)-or
-C (= NOR^Ten)-(Wherein R^TenIs a hydrogen atom, C₁-C₆
Alkyl group, halo C₁-C₆Alkyl group, C₃-C₆Alkenyl
Group, halo c₃-C₆Alkenyl group, C₃-C₆Alkynyl group, ha
B C₃-C₆Alkynyl group, C₃-C₆Cycloalkyl group,
Nil C₁-C_FourAlkyl group or same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo C₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C ₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
A substituted phenyl having on the ring one or more substituents selected from
Nil C₁-C_FourIndicates an alkyl group. ), And R⁸Is hydrogen
Child, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₃-C₆
Alkenyl group, halo C₃-C₆Alkenyl group, C₃-C₆Archi
Nyl group, halo C₃-C₆Alkynyl group, C₃-C₆Cycloalk
Ru radical, C₁-C₆Alkylcarbonyl group, halo C₁-C₆Archi
Lecarbonyl group, C₁-C₆Alkoxycarbonyl group, mono
 C₁-C₆Alkylaminocarbonyl group, the same or different
Also good C₁-C₆Alkylaminocarbonyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁
-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C
₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted phenyl group having a substituent, phenyl C₁-C_FourAlkyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted phenyl C having a substituent on the ring₁-C_FourAlkyl group, multiple
It may be a cyclic group or the same or different and may be a halogen atom.
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C ₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C ₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
A substituted heterocyclic group having one or more substituents is shown. )
You ) Is shown. Also, R¹Is A¹Combined with one or two
Oxygen atom, sulfur atom or nitrogen source which may be the same or different
To form a 5- to 8-membered ring which may be interrupted by the child
it can. R²And R³May be the same or different, and hydrogen
Atom, C₃-C₆Cycloalkyl group or -A²-R^Four(In the formula,
A²And R^FourIs the same as above. ) Is shown. Also, R²Is A¹
Or R¹1 to 2 same or different may be combined with
Even if interrupted by oxygen, sulfur or nitrogen atoms
A good 5- to 7-membered ring can be formed. X is the same or
May be different, halogen atom, cyano group, nitro group,
 C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalkyl
Base, C₁-C₆Alkoxycarbonyl group, phenyl group, same
Or may be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group, halo C₁-C₆Alkylsul
Honyl group, Mono C₁-C₆Alkylamino group, same or different
I'm good C₁-C₆Alkylamino group or C₁-C₆Arco
Having one or more substituents selected from oxycarbonyl groups
Substituted phenyl group, heterocyclic group, same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo C₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C ₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
A substituted heterocyclic group having one or more substituents selected from
Is -A³-R¹¹(In the formula, A³ Is -O-, -S-, -SO
-, -SO₂-, -C (= O)-, -C (= NOR¹²)
-(In the formula, R¹²Is a hydrogen atom, C₁-C₆Alkyl group, halo C
₁-C₆Alkyl group, C₃-C₆Alkenyl group, halo C₃-C₆Al
Kenyl group, C₃-C₆Alkynyl group, C₃-C₆Cycloalkyl
Group, phenyl C₁-C_FourAlkyl group or same or different
May be, halogen atom, cyano group, nitro group, C₁-C₆
Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆Al
Killsulfonyl group, halo C₁-C₆An alkylsulfonyl group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group or C₁-C₆Alkoxy carbo
An arrangement having on the ring one or more substituents selected from the group nyl.
Converted phenyl C₁-C_FourIndicates an alkyl group. ), C₁-C₆Archi
Ren group, halo C₁-C₆Alkylene group, C₂-C₆Alkenylene
Group, halo c₂-C₆Alkenylene group, C₂-C₆Alkynylene group
Or halo C₃-C₆An alkynylene group, (1) A³But-
O-, -S-, -SO- or -SO₂-Indicates R
¹¹Is halo c₃-C₆Cycloalkyl group, halo C₃-C₆Cycloa
Lucenyl group, phenyl group, which may be the same or different,
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rualkylamino group, di-C which may be the same or different₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C ₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
Substituted heterocyclic group having a substituent or -A^Four-R¹³(In the formula, A^Four
Is C₁-C₆Alkylene group, halo C₁-C₆Alkylene group, C₃-
C₆Alkenylene group, halo C₃-C₆Alkenylene group, C₃-C₆
Alkynylene group or halo C₃-C₆Represents an alkynylene group,
R¹³Is hydrogen atom, halogen atom, C ₃-C₆Cycloalkyl
Group, halo c₃-C₆Cycloalkyl group, C₁-C₆Alkoxyca
Rubonyl group, phenyl group, which may be the same or different,
Rogen atom, cyano group, nitro group, C₁-C₆An alkyl group,
Halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C ₁-
C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆A
Rukiruthio group, C₁-C₆Alkylsulfinyl group, halo C
₁-C₆Alkylsulfinyl group, C₁-C₆Alkyl sulfoni
Lu group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-C₆A
Rukylamino group, which may be the same or different, di C₁-C₆Al
Kiramino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted phenyl group having one or more selected substituents or-
A^Five-R¹⁴(In the formula, A^FiveIs -O-, -S-, -SO-,-
SO₂-Or-C (= O) -indicates R¹⁴Is C₁-C₆Al
Kill group, halo C₁-C₆Alkyl group, C₃-C₆An alkenyl group,
Halo c₃-C₆Alkenyl group, C₃-C₆Alkynyl group, halo C
₃-C₆Alkynyl group, C₃-C₆Cycloalkyl group, halo C₃-
C₆Cycloalkyl group, phenyl group, the same or different
Well, halogen atom, cyano group, nitro group, C₁-C₆Al
Kill group, halo C₁-C₆Alkyl group, C₁-C₆An alkoxy group,
Halo c₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo
 C₁-C₆Alkylthio group, C₁-C₆Alkylsulfinyl
Group, halo c₁-C₆Alkylsulfinyl group, C₁-C₆Archi
Lesulfonyl group, halo C₁-C₆Alkylsulfonyl group,
No C₁-C₆An alkylamino group, which may be the same or different
 C₁-C₆Alkylamino group or C₁-C₆Alkoxy Carboni
Substituted phenyl having one or more substituents selected from
Group, heterocyclic group or the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Is a substituted heterocyclic group having one or more substituents. )
Indicates (2) A³ Is -C (= O)-or -C (= NO
R¹²)-(Wherein R¹²Is the same as above. ) Indicates R
¹¹Is a hydrogen atom, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₂-C₆Alkenyl group, halo C₂-C₆Alkenyl group, C
₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalkyl group,
 C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, Mono C₁-C
₆Alkylamino group, which may be the same or different, di C₁-C₆
Alkylamino group, phenyl group, same or different
, Halogen atom, cyano group, nitro group, C ₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
Substituted phenyl having one or more substituents selected from
Groups, phenylamino groups, which may be the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Substituted Phenylamido Having One or More Substituents on the Ring
Group, a heterocyclic group, or the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Killamino group, di-C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
A substituted heterocyclic group having one or more substituents,
(3) A³ Is C₁-C₆Alkylene group, halo C₁-C₆Arche
Group, C₂-C₆Alkenylene group, halo C₂-C₆Alkenylene
Base, C₂-C₆Alkynylene group or halo C₃-C₆Alkynylene
When a group is shown, R¹¹Is a hydrogen atom, hydroxy group, halogen
Atom, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloa
Rukiru group, C₁-C₆Alkoxycarbonyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C ₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Heterocyclic group or -A⁶-R¹⁵(In the formula, A⁶ Is -O-, -S
-, -SO- or -SO₂-Indicates R¹⁵Is C₃-C₆Shiku
Lower alkyl group, halo C₃-C₆Cycloalkyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Heterocyclic group or -A⁷-R¹⁶(In the formula, A⁷ Is C ₁-C₆Arche
Group, halo C₁-C₆Alkylene group, C₂-C₆Alkenylene
Group, halo c₂-C₆Alkenylene group, C₂-C₆Alkynylene group
Or halo C₃-C₆Represents an alkynylene group, R¹⁶Is hydrogen
Child, halogen atom, C₃-C₆Cycloalkyl group, halo C₃-
C₆Cycloalkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, phenyl group,
One or different, halogen atom, cyano group, nit
B, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-
C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Al
Kirthio group, halo C₁-C₆Alkylthio group, C ₁-C₆Archi
Rusulfinyl group, halo C₁-C₆Alkylsulfinyl
Base, C₁-C₆Alkylsulfonyl group, halo C₁-C₆Alkyl
Sulfonyl group, mono C₁-C₆Alkylamino group, same or
It may be different C₁-C₆Alkylamino group or C₁-C₆A
One or more substituents selected from lucoxycarbonyl groups
Having a substituted phenyl group, a phenoxy group, the same or different
May be, halogen atom, cyano group, nitro group, C₁-C₆
Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆Al
Killsulfonyl group, halo C₁-C₆An alkylsulfonyl group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group or C₁-C₆Alkoxy carbo
Substituted Fe having one or more substituents selected from the group
A nonoxy group, a phenylthio group, which may be the same or different,
Halogen atom, cyano group, nitro group, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C
₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group, halo C₁-C₆Alkylsulfonyl group, Mono C₁-
C₆Alkylamino group, which may be the same or different, di C ₁-C₆
Alkylamino group or C₁-C₆Is it an alkoxycarbonyl group?
Substituted phenylthio having one or more substituents selected from
Groups, heterocyclic groups or the same or different, halogen
Atom, cyano group, nitro group, C₁-C₆Alkyl group, halo
 C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆A
Lucoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Archi
Ruthio group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆
Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Is a heterocyclic group having one or more substituents. )
You ) Is shown and l shows the integer of 0-4. Also, X is
A fused ring together with adjacent carbon atoms on the nyl ring
Can be formed and the fused rings can be the same or different.
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁
-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
It can also have one or more substituents selected from
Y may be the same or different, and a halogen atom, cyano
Group, nitro group, halo C₃-C₆A cycloalkyl group, the same or
May be different C₁-C₆Alkylsilyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group or C
₁-C₆One or more positions selected from alkoxycarbonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Heterocyclic group or -A³-R¹¹(In the formula, A³ And R¹¹Is above
the same. ) Is shown and m shows the integer of 0-5. Also, Y is
Fused ring with adjacent carbon atoms on the phenyl ring
And the fused rings may be the same or different.
Well, halogen atom, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
C₁-C₆Alkylsulfonyl group, phenyl group, same or different
Can be halogen atom, cyano group, nitro group, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arco
Xy, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group, halo C₁-C₆Alkylsulfonyl
Group, Mono C ₁-C₆Alkylamino group, the same or different
Good the C₁-C₆Alkylamino group or C₁-C₆Alkoxyca
Substitutions having one or more substituents selected from the group
Phenyl group, heterocyclic group or same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C ₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
A substituted heterocyclic group having one or more substituents selected from
It can also have one or more substituents selected from n
Represents an integer of 0 to 2. However, it is represented by the general formula (I).
The phthalamide derivative is N²-(1,1-dimethyl-2-me
Tylthioethyl) -3-iodo-N¹-{2-methyl-
4- [1,2,2,2-tetrafluoro-1- (trif
Luoromethyl) ethyl] phenyl} phthalamide, N²
-(1,1-dimethyl-2-methylsulfonylethyl)
-3-Iodo-N¹-{2-methyl-4- [1,2,
2,2-tetrafluoro-1- (trifluoromethyl)
Ethyl] phenyl} phthalamide or N²-(1,1-
Dimethyl-2-methylsulfinylethyl) -3-io
DO-N¹-{2-methyl-4- [1,2,2,2-teto
Rafluoro-1- (trifluoromethyl) ethyl] fe
Nil} phthalamide is excluded. }
Contains a taramide derivative or its salt as an active ingredient
An agricultural and horticultural insecticide characterized by the following. 5. A¹Is C₁-C₈Alkylene group, same or different
Halogen atom, halo C₁-C₆An alkyl group,
 C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group, halo C₁-C₆Archi
Lesulfonyl group, C₁-C₆Alkylthio C₁-C₆Alkyl
Groups, phenyl groups or may be the same or different, halo
Gen atom, C₁-C₆Alkyl group, halo C₁-C₆An alkyl group,
 C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Al
Having one or more substituents selected from a sulfonyl group
Have one or more substituents selected from substituted phenyl groups
Substitution C₁-C₈Alkylene group, C₃-C₈Alkenylene group,
May be one or different, halogen atom, halo C₁-C₆Al
Kill group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, halo
 C₁-C₆Alkylsulfonyl group or C ₁-C₆Alkylthio C
₁-C₆Having one or more substituents selected from alkyl groups
Substitution C₃-C₈Alkenylene group, C₃-C₈ Alkynylene group or
May be the same or different, halogen atom, halo C₁-C
₆ Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group or C₁-C₆Alkylthio
 C₁-C₆Have one or more substituents selected from alkyl groups
Substitution C₃-C₈An alkynylene group,₁-C₈Archi
Ren group, substituted C₁-C₈Alkylene group, C₃-C₈Alkenylene
Group, substituted C₃-C₈Alkenylene group, C₃-C₈ Alkynylene group
Or substitution C₃-C₈Any saturated carbon atom in the alkynylene group
Is C₂-C_FiveC substituted with an alkylene group₃-C₆Cycloalca
Can also be represented by the C₁-C₈Alkylene group, substituted
 C₁-C₈Alkylene group, C₃-C₈Alkenylene group, substituted C₃-
C₈Any two carbon atoms in the alkenylene group are alkyle
C together with benzene or alkenylene groups₃-C₆Cycloa
Lucan ring or C₃-C₆Can also represent a cycloalkene ring
It R¹Is a hydrogen atom, mercapto group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C₃-C₆Cycloalk
Lu group, halo C₃-C₆Cycloalkyl group, phenyl group, same
Or may be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C ₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group, halo C ₁-C₆Alkylsul
Honyl group, Mono C₁-C₆Alkylamino group, same or different
I'm good C₁-C₆Alkylamino group or C₁-C₆Arco
Having one or more substituents selected from oxycarbonyl groups
Substituted phenyl group, phenylthio group, the same or different
Also good, halogen atom, cyano group, nitro group, C₁-C₆A
Rukiru group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆Al
Killsulfonyl group, halo C₁-C₆An alkylsulfonyl group,
Mono C₁-C₆Alkylamino group, which may be the same or different
The C₁-C₆Alkylamino group or C₁-C₆Alkoxy carbo
Substituted Fe having one or more substituents selected from the group
Nylthio group, heterocyclic group, which may be the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C ₁-C₆Select from alkoxycarbonyl groups
Substituted heterocyclic group having one or more substituents or -A²-
R^Four(In the formula, A² Is -C (= O)-, -C (= S)-,
-C (= NR^Five)-(Wherein R^FiveIs a hydrogen atom, C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Noki, C₁-C₆Alkoxycarbonyl group, phenyl group or
May be the same or different, halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
The substituted phenyl group is shown. ), C₁-C₈Alkylene
Group, halo c₁-C₈Alkylene group, C₃-C₆Alkenylene group,
Halo c₃-C₆Alkenylene group, C₃-C₆Alkynylene group or
Halo c₃-C₆An alkynylene group, (1) A² Is -C
(= O)-, -C (= S)-or -C (= NR^Five) −
(In the formula, R^FiveIs the same as above. ) Indicates R^FourIs hydrogen
Atom, C₁-C₆Alkyl group, halo C ₁-C₆Alkyl group, C₃-
C₆Cycloalkyl group, halo C₃-C₆Cycloalkyl group,
Phenyl group, which may be the same or different, a halogen atom,
Ano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Al
Kill group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
A substituted phenyl group having a substituent, a heterocyclic group, the same or different
Can be halogen atom, cyano group, nitro group, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arco
Xy, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C ₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆ 
Alkylsulfonyl group or halo C₁-C₆Alkyl sulfoni
Substituted heterocycle having one or more substituents selected from the group
Group or -Z¹-R⁶(In the formula, Z¹ Is -O-, -S- or-
N (R⁷)-(Wherein R⁷Is a hydrogen atom, C₁-C₆Alkyl
Base, C₁-C₆Alkylcarbonyl group, halo C₁-C₆Alkyl
Carbonyl group or C₁-C₆Indicates an alkoxycarbonyl group
You ), And R⁶Is a hydrogen atom, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₃-C₆Alkenyl group, halo C₃-C₆
Alkenyl group, C₃-C₆Alkynyl group, halo C₃-C₆Archi
Nyl group, C₃-C₆Cycloalkyl group, phenyl group, same or
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
C₁-C₆ Alkylsulfonyl group or halo C₁-C₆Alkyls
Substitution with one or more substituents selected from the group
Phenyl group, Phenyl C ₁-C_FourAlkyl group, same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group or halo C₁-C₆Alkyl sulfoni
Substituted with one or more substituents selected from
Phenyl C₁-C_FourAlkyl group, heterocyclic group or the same or
May be different, halogen atom, cyano group, nitro group,
 C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Al
Coxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C₁-C₆Alkylsul
Finyl group, halo C₁-C₆Alkylsulfinyl group, C₁-
C₆Alkylsulfonyl group or halo C₁-C₆Alkyl sulfo
Substituted heterocycle having one or more substituents selected from nyl group
Indicates a ring group. ), And (2) A² Is C₁-C₈Alkylene
Group, halo c₁-C₈Alkylene group, C₃-C₆Alkenylene group,
Halo c₃-C₆Alkenylene group, C₃-C₆Alkynylene group or
Halo c₃-C₆When an alkynylene group is shown, R^FourIs hydrogen
Child, halogen atom, cyano group, nitro group, C ₃-C₆Cyclo
Alkyl group, halo C₃-C₆Cycloalkyl group, C₁-C₆Al
Coxycarbonyl group, mono C₁-C₆Alkylaminocarbo
Nyl group, which may be the same or different, di C ₁-C₆Alkylami
Nocarbonyl group, phenyl group, the same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C ₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Rufonyl group or halo C₁-C₆Select from alkylsulfonyl group
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
A substituted heterocyclic group having -Z²-R⁸(In the formula, Z² Is -O
-, -S- -SO- -SO₂-, -N (R⁹)-(Expression
Medium, R⁹Is a hydrogen atom, C₁-C₆Alkyl group, C₁-C₆Archi
Lucarbonyl group, halo C ₁-C₆Alkylcarbonyl group, C
₁-C₆Alkoxycarbonyl group, phenylcarbonyl group or
May be the same or different, and may be a halogen atom, cyano
Group, nitro group, C ₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
The substituted phenylcarbonyl group is shown. ), -C (=
O)-or -C (= NOR^Ten-(In the formula, R^TenIs hydrogen
Child, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₃-C₆
Alkenyl group, halo C₃-C₆Alkenyl group, C₃-C₆Archi
Nyl group, halo C₃-C₆Alkynyl group, C₃-C₆Cycloalk
Group, phenyl C₁-C_FourAlkyl group or same or different
Halogen atom, cyano group, nitro group, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulf
Inyl group, halo C₁-C₆Alkylsulfinyl group, C₁-C₆
Alkylsulfonyl group or halo C₁-C₆Alkyl sulfoni
Substituted with one or more substituents selected from
Phenyl C₁-C_FourIndicates an alkyl group. ), And R⁸Is water
Elementary atom, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₃-C₆Alkenyl group, halo C₃-C₆Alkenyl group, C₃-C₆A
Lucinyl group, halo C₃-C₆Alkynyl group, C₃-C₆Cycloa
Rukiru group, C₁-C₆Alkylcarbonyl group, halo C₁-C₆A
Rukylcarbonyl group, C₁-C₆An alkoxycarbonyl group,
Mono C₁-C₆Alkylaminocarbonyl group, same or different
I'm good C₁-C₆Alkylaminocarbonyl group,
Nyl group, which may be the same or different, may be a halogen atom or a sialic group.
No group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Archi
Ru radical, C₁-C₆Alkoxy group, halo C₁-C₆An alkoxy group,
 C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C
₁-C₆Alkylsulfinyl group, halo C₁-C₆Alkylsul
Finyl group, C₁-C₆Alkylsulfonyl group or halo C₁-
C₆One or more substituents selected from alkylsulfonyl groups
A substituted phenyl group having phenyl C₁-C_FourAn alkyl group,
They may be the same or different and may be a halogen atom, a cyano group, or
Toro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆A
Rukiruthio group, halo C₁-C₆Alkylthio group, C₁-C₆Al
Kirsulfinyl group, halo C₁-C₆Alkylsulfinyl
Base, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Archi
On the ring one or more substituents selected from
Substituted phenyl C having₁-C_FourAlkyl group, heterocyclic group or the same
One or different, a halogen atom, a cyano group,
Nitro group, C₁-C₆Alkyl group, halo C₁-C₆An alkyl group,
 C ₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Al
Having one or more substituents selected from a sulfonyl group
Represents a substituted heterocyclic group. ) Is shown. ) Is shown. Also, R¹
Is A¹1 or 2 may be the same or different by combining with
It may be interrupted by oxygen, sulfur or nitrogen atoms.
A 5- to 8-membered ring can be formed. R²And R³Is
May be the same or different, hydrogen atom, C₃-C₆ Cycloal
Kill group or -A²-R^Four(In the formula, A²And R^FourIs the same as above
Same. ) Is shown. Also, R²Is A¹Or R¹Combined with 1
Up to two identical or different oxygen atoms, sulfur atoms or
Form a 5-7 membered ring which may be interrupted by a nitrogen atom
You can X may be the same or different, and
Atom, cyano group, nitro group, C₁-C₆Alkyl group, halo
 C₁-C₆Alkyl group, C₂-C₆Alkenyl group, halo C₂-C₆A
Lucenyl group, C₂-C₆Alkynyl group, halo C₂-C₆Alkini
Ru radical, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloal
Kill group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group, C₁-
C₆Alkylsulfonyl group or C₁-C₆Alkoxy Carboni
Group, and l represents an integer of 0 to 4. Also, X is pheny
Form a fused ring with adjacent carbon atoms on the ring.
The condensed rings may be the same or different.
Black, halogen atom, C₁-C₆Alkyl group, halo C₁-C₆Al
Kill group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
It can also have a substituent. Y may be the same or different
Well, halogen atom, cyano group, nitro group, halo C₃-C₆
A cycloalkyl group, which may be the same or different, tri C₁-C₆
Alkylsilyl group, phenyl group, same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Rufonyl group or halo C₁-C₆Select from alkylsulfonyl group
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C
₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
A substituted heterocyclic group having -A³-R¹¹(In the formula, A³ Is -O
-, -S-, -SO-, -SO₂-, -C (= O)-,-
C (= NOR¹²)-(Wherein R¹²Is a hydrogen atom, C₁-C₆A
Rukiru group, halo C₁-C₆Alkyl group, C₃-C₆Alkenyl
Group, halo c₃-C₆Alkenyl group, C₃-C₆Alkynyl group, C₃
-C₆Cycloalkyl group, phenyl C₁-C_FourAlkyl group or the same
One or different, a halogen atom, a cyano group,
Nitro group, C₁-C₆Alkyl group, halo C₁-C₆An alkyl group,
 C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C ₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Al
Having one or more substituents selected from a sulfonyl group
Phenyl C₁-C_FourIndicates an alkyl group. ), C₁-C₆Archi
Ren group, halo C₁-C₆Alkylene group, C₂-C₆Alkenylene
Group, halo c₂-C₆Alkenylene group, C ₂-C₆Alkynylene group
Or halo C₃-C₆An alkynylene group, (1) A³But-
O-, -S-, -SO- or -SO₂-Indicates R
¹¹Is a phenyl group, which may be the same or different and may be a halogen source.
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group or
Halo c₁-C₆One or more selected from alkylsulfonyl groups
A substituted phenyl group having a substituent of, a heterocyclic group, the same or
May be different, halogen atom, cyano group, nitro group,
 C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Al
Coxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C ₁-C₆Alkylsul
Finyl group, halo C₁-C₆Alkylsulfinyl group, C₁-
C₆Alkylsulfonyl group or halo C₁-C₆Alkyl sulfo
Substituted heterocycle having one or more substituents selected from nyl group
Ring group or -A^Four-R¹³(In the formula, A^FourIs C₁-C₆Alkylene
Group, halo c₁-C₆Alkylene group, C₃-C₆Alkenylene group,
Halo c₃-C₆Alkenylene group, C₃-C₆Alkynylene group or
Halo c₃-C₆Represents an alkynylene group, R¹³Is a hydrogen atom,
Rogen atom, C₃-C₆Cycloalkyl group, halo C₃-C₆Shiku
Alkyl group, phenyl group, may be the same or different,
Halogen atom, cyano group, nitro group, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
 C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-
C₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group or halo C₁-C₆Select from alkylsulfonyl groups
Substituted phenyl group having one or more substituents or -A
^Five-R¹⁴(In the formula, A^FiveIs -O-, -S-, -SO-, -S
O ₂-Or-C (= O) -indicates R¹⁴Is C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₃-C₆Alkenyl group, ha
B C₃-C₆Alkenyl group, C₃-C₆Alkynyl group, halo C₃-C
₆Alkynyl group, C₃-C₆Cycloalkyl group, halo C₃-C₆
Cycloalkyl group, phenyl group, same or different
, Halogen atom, cyano group, nitro group, C ₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Rufonyl group or halo C₁-C₆Select from alkylsulfonyl group
A substituted phenyl group having one or more selected substituents, a hetero group
Cyclic groups or the same or different, a halogen atom,
Cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆A
Rukiru group, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
A substituted heterocyclic group having a substituent is shown. ), And (2)
A³ Is -C (= O)-or -C (= NOR¹²) (Where
R¹²Is the same as above. ) Indicates R¹¹Is a hydrogen atom, C
₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₂-C₆Arche
Nyl group, halo C₂-C₆Alkenyl group, C₃-C₆Cycloalk
Lu group, halo C₃-C₆Cycloalkyl group, C₁-C₆Alkoxy
Base, C₁-C₆Alkylthio group, Mono C ₁-C₆Alkylamino
Groups, which may be the same or different, di C₁-C₆Alkylamino
Groups, phenyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group or
Halo c₁-C₆One or more selected from alkylsulfonyl groups
A substituted phenyl group having a substituent of, a phenylamino group,
They may be the same or different and may be a halogen atom, a cyano group, or
Toro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆A
Rukiruthio group, halo C₁-C₆Alkylthio group, C₁-C₆Al
Kirsulfinyl group, halo C₁-C₆Alkylsulfinyl
Base, C₁-C₆Alkylsulfonyl group or halo C₁-C₆Archi
On the ring one or more substituents selected from
Having a substituted phenylamino group, a heterocyclic group or the same or younger
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group or halo C₁-C₆Alkyls
Substitution with one or more substituents selected from the group
Represents a heterocyclic group, (3) A³ Is C₁-C₆Alkylene group, ha
B C₁-C₆Alkylene group, C₂-C₆Alkenylene group, halo C
₂-C₆Alkenylene group, C₂-C₆Alkynylene group or halo C
₃-C₆When an alkynylene group is shown, R¹¹Is a hydrogen atom, hydr
Roxy group, halogen atom, C₃-C₆Cycloalkyl group, ha
B C₃-C₆Cycloalkyl group, C₁-C₆Alkoxy Carboni
Group, phenyl group, same or different, halogen
Atom, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁
-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Al
Coxy group, C₁-C₆Alkylthio group, halo C₁-C₆Alkyl
Thio group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆A
Rukylsulfinyl group, C₁-C₆Alkylsulfonyl group
Is halo c₁-C₆1 or more selected from alkylsulfonyl groups
A substituted phenyl group having the above substituent, a heterocyclic group, the same or
May be different, halogen atom, cyano group, nitro
Base, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆
Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylthio group, C₁-C₆Alkyl
Sulfinyl group, halo C₁-C₆An alkylsulfinyl group,
 C₁-C₆Alkylsulfonyl group or halo C₁-C₆Alkyls
Substitution with one or more substituents selected from the group
Heterocyclic group or -A⁶-R¹⁵(In the formula, A⁶ Is -O-, -S
-, -SO- or -SO₂-Indicates R¹⁵Is C₃-C₆Shiku
Lower alkyl group, halo C₃-C₆Cycloalkyl group, phenyl
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C ₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
Having a substituted phenyl group, a heterocyclic group, the same or different
Well, halogen atom, cyano group, nitro group, C₁-C₆Al
Kill group, halo C₁-C₆Alkyl group, C₁-C₆An alkoxy group,
Halo c₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo
C₁-C₆Alkylthio group, C₁-C₆Alkylsulfinyl
Group, halo c₁-C₆Alkylsulfinyl group, C₁-C₆Archi
Sulfonyl group or halo C₁-C₆Alkylsulfonyl group
A substituted heterocyclic group having one or more substituents selected from
-A⁷-R¹⁶(In the formula, A⁷ Is C₁-C₆Alkylene group, halo C
₁-C₆Alkylene group, C₂-C₆Alkenylene group, halo C₂-C₆
Alkenylene group, C₂-C₆Alkynylene group or halo C₃-C₆
Represents an alkynylene group, R¹⁶Is hydrogen atom, halogen atom
Child, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalk
Ru radical, C₁-C₆Alkoxy group, halo C₁-C₆An alkoxy group,
 C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C
₁-C₆Alkylsulfinyl group, halo C₁-C₆Alkylsul
Finyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆
Alkylsulfonyl group, phenyl group, the same or different
Also good, halogen atom, cyano group, nitro group, C₁-C₆A
Rukiru group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy
Group, halo c₁-C₆Alkoxy group, C₁-C₆An alkylthio group,
Halo c₁-C₆Alkylthio group, C₁-C₆Alkylsulfini
Lu group, halo C₁-C₆Alkylsulfinyl group, C ₁-C₆Al
Killsulfonyl group or halo C₁-C₆Alkylsulfonyl group
Substituted phenyl having one or more substituents selected from
Groups, phenoxy groups, which may be the same or different, halogen
Atom, cyano group, nitro group, C₁-C₆Alkyl group, halo C
₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Al
Coxy group, C₁-C₆Alkylthio group, halo C₁-C₆Alkyl
Thio group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆A
Rukylsulfinyl group, C₁-C₆Alkylsulfonyl group
Is halo c₁-C₆1 or more selected from alkylsulfonyl groups
Substituted phenoxy group having the above substituent, phenylthio
Groups, which may be the same or different, a halogen atom, cyano
Group, nitro group, C₁-C₆Alkyl group, halo C₁-C₆Alkyl
Base, C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C
₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C₁-
C₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group or halo C₁-C₆
One or more substituents selected from alkylsulfonyl groups
Having a substituted phenylthio group, a heterocyclic group or the same or
May be different, halogen atom, cyano group, nitro group,
 C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Al
Coxy group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylchi
O group, halo C₁-C₆Alkylthio group, C₁-C₆Alkylsul
Finyl group, halo C₁-C₆Alkylsulfinyl group, C₁-
C₆Alkylsulfonyl group or halo C₁-C₆Alkyl sulfo
Heterocyclic group having one or more substituents selected from nyl group
Indicates. ) Is shown. ), M is an integer of 1 to 5
You Also, Y is the same as the adjacent carbon atom on the phenyl ring.
To form a condensed ring, and the condensed rings are the same.
Or may be different, halogen atom, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
 C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C
₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group or halo C₁-C₆Select from alkylsulfonyl groups
Can have one or more substituents, and n is 0 to 2
The phthalamide derivative or its derivative according to claim 4, which represents an integer of
An agricultural and horticultural insecticide containing salt as an active ingredient. 6. A¹Is C₁-C₈Alkylene group, same or different
Halogen atom, halo C₁-C₆An alkyl group,
 C₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆
Alkylthio group, halo C₁-C₆Alkylthio group, C₁-C₆A
Rukylsulfinyl group, halo C₁-C₆Alkylsulfini
Ru radical, C₁-C₆Alkylsulfonyl group, halo C₁-C₆Archi
Lesulfonyl group or C₁-C₆Alkylthio C₁-C₆Alkyl
Substituted C having one or more substituents selected from the group₁-C₈A
Represents a alkylene group, and₁-C₈Alkylene group or substituted C
₁-C₈Any saturated carbon atom in the alkylene group is C₂-C_FiveAl
C substituted with a xylene group₃-C₆Indicates a cycloalkane ring
You can also do the above C₁-C₈Alkylene group or C₁-C₈Arche
Any two carbon atoms in the phenyl group together with the alkylene group
Become C₃-C₆It can also represent a cycloalkane ring. R
¹Is a hydrogen atom, mercapto group, C₁-C₆Alkyl group, halo
 C₁-C₆Alkyl group, C₃-C₆Alkenyl group, halo C₃-C₆A
Lucenyl group, C₃-C₆Alkynyl group, halo C₃-C₆Alkini
Ru radical, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloal
Kill group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkoxy C₁-C₆Alkyl group, C₁-C₆Al
Kircio C₁-C₆Alkyl group, Mono C₁-C₆Alkylamino
 C₁-C₆Alkyl groups, which may be the same or different, di C₁-C₆A
Rukiruamino C₁-C₆Alkyl group, C₁-C₆Alkyl carbo
Nyl group, halo C₁-C₆Alkylcarbonyl group, C₁-C₆Al
Kirthiocarbonyl group, C₁-C₆Alkoxy carbonyl
Group, Mono C₁-C₆Alkylaminocarbonyl group, the same or
It may be different C₁-C₆An alkylaminocarbonyl group,
Mono C₁-C₆Alkylaminothiocarbonyl group, the same or
It may be different C ₁-C₆Alkylaminothiocarbonyl
Base, C₁-C₆Alkylcarbonyl C₁-C₆Alkyl group, C₁-
C₆Alkoxyimino C₁-C₆Alkyl group, C₁-C₆Arcoki
Sicarbonyl C₁-C₆Alkyl group, Mono C₁-C₆Alkyla
Minocarbonyl C₁-C₆Alkyl groups, whether identical or different
Good the C₁-C₆Alkylaminocarbonyl C₁-C₆Alkyl
Groups, phenyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
Substituted phenyl group having one or more substituents, phenyl C₁-
C₆Alkyl groups, which may be the same or different, may be halogenated
Child, cyano group, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylchi
O group, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Al
Kirsulfinyl group, C₁-C₆Alkylsulfonyl group,
B C₁-C₆Alkylsulfonyl group, Mono C₁-C₆Alkyla
Mino groups, which may be the same or different, di C₁-C₆Alkylami
Group or C₁-C₆Selected from alkoxycarbonyl groups
Substituted Phenyl C Having One or More Substituents on the Ring₁-C₆Al
Kill group, phenylcarbonyl group, same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
Substituted phenyl group having one or more substituents selected from
Rubonyl group, phenylthio group, same or different
, Halogen atom, cyano group, nitro group, C₁-C₆Archi
Lu group, halo C₁-C₆Alkyl group, C₁-C₆Alkoxy group, ha
B C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C
₁-C₆Alkylthio group, C₁-C₆An alkylsulfinyl group,
Halo c₁-C₆Alkylsulfinyl group, C₁-C₆Alkyls
Ruphonyl group, halo C₁-C₆Alkylsulfonyl group, Mono C
₁-C₆Alkylamino group, which may be the same or different, di C₁-
C₆Alkylamino group or C₁-C₆Alkoxycarbonyl group
A substituted phenyl group having one or more substituents selected from
An o group, a heterocyclic group, or the same or different, halo
Gen atom, cyano group, nitro group, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, C₁-C₆Alkylsulfinyl group, halo C₁-
C₆Alkylsulfinyl group, C₁-C₆Alkylsulfonyl
Group, halo c₁-C₆Alkylsulfonyl group, Mono C₁-C₆Al
Kiramino group, di C which may be the same or different₁-C₆Archi
Luamino group or C₁-C₆Select from alkoxycarbonyl groups
Is a substituted heterocyclic group having one or more substituents.
Also, R¹Is A¹Combined with 1 or 2 identical or different
May be interrupted by an oxygen atom, sulfur atom or nitrogen atom.
It may form a 5- to 8-membered ring which may be present. R²Over
And R³May be the same or different, and may be a hydrogen atom or C₁-C₆
Indicates an alkyl group. Also, R²Is A¹Or R¹Combined with
And 1 or 2 oxygen atoms which may be the same or different, sulfur
A 5-7 membered ring which may be interrupted by atoms or nitrogen atoms
Can be formed. X may be the same or different,
Halogen atom, nitro group, C₁-C₆Alkyl group, halo C₁-
C₆Alkyl group, C₂-C₆Alkenyl group, halo C₂-C₆Arche
Nyl group, C₂-C₆Alkynyl group, halo C₂-C₆Alkynyl
Base, C₃-C₆Cycloalkyl group, halo C₃-C₆Cycloalk
Ru radical, C₁-C₆Alkoxy group, halo C₁-C₆An alkoxy group,
 C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio group, C
₁-C₆Alkylsulfinyl group, halo C₁-C₆Alkylsul
Finyl group, C₁-C₆Alkylsulfonyl group or halo C₁-
C₆Represents an alkylsulfonyl group, and l represents an integer of 0 to 4
You Also, X is the same as the adjacent carbon atom on the phenyl ring.
To form a condensed ring, and the condensed rings are the same.
Or may be different, halogen atom, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
 C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C
₆Alkylthio group, C₁-C₆Alkylsulfinyl group, ha
B C₁-C₆Alkylsulfinyl group, C₁-C₆Alkylsul
Honyl group or halo C₁-C₆Select from alkylsulfonyl groups
It may also have one or more substituents as defined. Y is the same
Or may be different, halogen atom, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, hydroxyhalo C₁-C₆Al
Kill group, C₁-C₆Alkoxy halo C₁-C₆Alkyl group, C₁-
C₆Alkylthiohalo C₁-C₆Alkyl group, C₃-C₆Archeni
Lu group, halo C₃-C₆Alkenyl group, C₃-C₆An alkynyl group,
Halo c₃-C₆Alkynyl group, C₁-C₆Alkoxy group, halo C
₁-C₆Alkoxy group, C₁-C₆Alkoxy halo C₁-C₆Arco
Xyl group, C₁-C₆Alkylthiohalo C₁-C₆An alkoxy group,
Halo c₁-C₆Alkoxy halo C₁-C₆Alkoxy group, halo C₃
-C₆Alkenyloxy group, C₁-C₆Alkylthio group, halo
C₁-C₆Alkylthio group, halo C₁-C₆Alkoxy halo C₁-C
₆Alkylthio group, halo C₁-C₆Alkenylthio group, C₁-C
₆Alkylsulfinyl group, halo C₁-C₆Alkylsulf
Inyl group, C₁-C₆Alkylsulfonyl group, halo C₁-C₆A
Lucylsulfonyl group, Mono C₁-C₆Alkylamino group,
One or different di C₁-C₆Alkylamino group, C₁-
C₆Alkoxycarbonyl group, C₃-C₆Cycloalkyl group,
Halo c ₃-C₆Cycloalkyl group, phenyl group, same or different
Can be a halogen atom, C₁-C₆Alkyl group, halo
C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆A
Lucoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Archi
Luthio group, halo C₁-C₆Alkylsulfinyl group or halo
 C₁-C₆One or more positions selected from alkylsulfonyl groups
A substituted phenyl group having a substituent, a phenoxy group, the same or
May be different, halogen atom, C₁-C₆Alkyl group, ha
B C₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆
Alkoxy group, C₁-C₆Alkylthio group, halo C₁-C₆Al
Kirthio group, halo C₁-C₆Alkylsulfinyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
A substituted phenoxy group having a substituent, a phenylthio group,
May be one or different, halogen atom, C₁-C₆Alkyl
Group, halo c₁-C₆Alkyl group, C₁-C₆Alkoxy group, halo
C₁-C₆Alkoxy group, C₁-C₆Alkylthio group, halo C ₁-C
₆Alkylthio group, halo C₁-C₆Alkylsulfinyl group
Or halo C₁-C₆1 selected from alkylsulfonyl groups
Substituted phenylthio group having the above substituents, pyridylo
A xy group, which may be the same or different, a halogen atom, C₁-
C₆Alkyl group, halo C₁-C₆Alkyl group, C₁-C₆Arcoki
Si group, halo C₁-C₆Alkoxy group, C₁-C₆Alkylthio
Group, halo c₁-C₆Alkylthio group, halo C₁-C₆Alkyls
Rufinyl group or halo C₁-C₆From an alkylsulfonyl group
Substituted Pyridyloxy Having One or More Substituents Selected
Groups, pyridylthio groups, which may be the same or different,
Atom, C₁-C₆Alkyl group, halo C₁-C₆Alkyl group, C
₁-C₆Alkoxy group, halo C₁-C₆Alkoxy group, C₁-C₆A
Rukiruthio group, halo C₁-C₆Alkylthio group, halo C₁-C₆
Alkylsulfinyl group or halo C₁-C₆Alkyl sulfo
A substituted pyri having one or more substituents selected from the group nyl.
Represents a dilthio group, and m represents an integer of 1 to 5. Also, Y is
Fused together with adjacent carbon atoms on the phenyl ring
Can form a ring and the fused rings can be the same or different.
Also good, halogen atom, C₁-C₆Alkyl group, halo C₁-C₆
Alkyl group, C₁-C₆Alkoxy group, halo C₁-C₆Arcoki
Shi group, C₁-C₆Alkylthio group, halo C₁-C₆Alkylthio
Base, C₁-C₆Alkylsulfinyl group, halo C₁-C₆Archi
Rusulfinyl group, C₁-C₆Alkylsulfonyl group or ha
B C₁-C₆One or more selected from alkylsulfonyl groups
It may have a substituent, and n is an integer representing an integer of 0 to 2.
The phthalamide derivative or the salt thereof according to claim 5 is an active ingredient.
Toshino's agricultural and horticultural insecticide. 7. The target crop or soil is treated with an effective amount of the agricultural and horticultural insecticide according to claim 4, in order to protect useful crops from pests. How to use agricultural and horticultural insecticides.