WO1996033180A1

WO1996033180A1 - Oxazoline and thiazoline arthropodicides

Info

Publication number: WO1996033180A1
Application number: PCT/US1996/004478
Authority: WO
Inventors: Victor Ekow Amoo
Original assignee: E.I. Du Pont De Nemours And Company
Priority date: 1995-04-18
Filing date: 1996-04-01
Publication date: 1996-10-24
Also published as: AU5439196A; TW308595B; EP0821677A1; IL117513A0; BR9608107A; JPH11505213A

Abstract

Compounds of Formula (I), and their N-oxides and agriculturally-suitable salts, are disclosed which are useful as arthropodicides, wherein X is selected from the group C1-C4 alkylene, -(CH2)n-A-, -(CH2)p-A-CH2-, each group optionally substituted with one to four R4; Y and Z are independently selected from the group O and S; A is selected from the group O, S and NR10; R1 is selected from the group 1-2 halogen, C¿1?-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, S(O)tR?11¿, cyano and nitro; R2 is selected from the group H, 1-2 halogen, C¿1?-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, S(O)tR?11¿, cyano and nitro; m is 1 or 2; n is 1, 2 or 3; p is 1 or 2; and E, Q, R?4, R5, R10, R11¿, q and t are as defined in the text. Also disclosed are compositions containing the compounds of Formula (I) and a method for controlling arthropods which involves contacting the arthropods or their environment with an effective amount of a compound of Formula (I).

Description

TITLE

OXAZOLINE AND THIAZOLINE ARTHROPODICIDES

BACKGROUND OF THE INVENTION

This invention relates to certain oxazoline and thiazoline compounds, their N-oxides, agriculturally-suitable salts and compositions, and methods of their use as arthropodicides in both agronomic and nonagronomic environments.

The control of arthropod pests is extremely important in achieving high crop efficiency. Arthropod damage to growing and stored agronomic crops can cause significant reduction in productivity and thereby result in increased costs to the consumer. The control of arthropod pests in forestry, greenhouse crops, ornamentals, nursery crops, stored food and fiber products, livestock, household, and public and animal health is also important. Many products are commercially available for these purposes, but the need continues for new compounds which are more effective, less costly, less toxic, environmentally safer or have different modes of action.

U.S. 5,141,948 discloses insecticidal oxazolines and thiazolines of Formula i:

wherein:

R₁ and R₂ are independently H, halogen, lower alkyl, lower alkoxy, nitro, lower haloalkyl or lower haloalkoxy, provided that R₁ and R₂ are not simultaneously H;

R₃ is H, halogen, lower alkyl or lower alkoxy;

R₄ is alkyl having 7 or more carbon atoms, alkoxy having 7 or more carbon atoms, alkylthio, lower alkoxy-lower alkyl, lower alkoxy-lower alkoxy, alkenyloxy having 3 or more carbon atoms, lower alkynyloxy, tri(lower alkyl)silyl, cycloalkyl which may be substituted by a lower alkyl, or

B is a direct bond, O, lower alkylene, lower alkyleneoxy, lower alkylenedioxy or a di(lower alkyl)silyl;

Q is CH or Ν; n is 0-5;

each R₅ is independently halogen, alkyl, alkoxy, lower haloalkyl, lower haloalkoxy or tri(lower alkyl)silyl;

A is a direct bond or lower alkylene; and

Z is O or S.

U.S. 4,977,171 discloses insecticidal and acaricidal oxazoline or thiazoline derivatives of Formula ii:

wherein:

X¹ and X² are independently H, lower alkyl, lower alkoxy, halogen,

trifluoromethyl or trifluoromethoxy;

Y¹ and Y² are independently H, lower alkyl, lower alkoxy, lower alkylthio, cyano, nitro, halogen or trifluoromethyl;

Z is O or S; and

n is 0 or 1.

WO 95/04726 discloses insecticidal and acaricidal oxazoline and thiazoline derivatives of Formula iii:

wherein, inter alia,

A is selected from the group a direct bond and C₁-C₃ straight or branched chain alkylene;

R³ is selected from the group C₃-C₇ halocycloalkyl; C₂-C₁₀ haloalkenyl optionally substituted with at least one member independently selected from the group cyano and C₂-C₆ alkoxycarbonyl; C₁ -C₁₀ alkyl substituted with at least one member independently selected from the group Si(R⁶)(R⁷)R⁸, cyano, C₂-C₆ alkylcarbonyl, C₂-C₆ haloalkylcarbonyl, C₂-C₆ haloalkoxycarbonyl, and C₂-C₆ alkoxycarbonyl; C₂-C₆ alkylcarbonyl; C₂-C₁₀ alkenyl optionally substituted with at least one member independently selected from R⁹; C₂-C₁₀ alkynyl optionally substituted with at least one member independently selected from R⁹; C₂-C₆ haloalkylcarbonyl; C₂-C₆ alkoxycarbonyl; C₂-C₆ haloalkoxycarbonyl; C(O)R⁹; C(O)OR⁹; C(O)N(R¹⁰)R^{1 1}; OR¹²; tetrahydropyranyl; phenyl substituted with at least one member independently selected from W¹; and an 8- to 12-membered fused bicyclic ring system containing 0-4 heteroatoms independently selected from 0-4 nitrogen, 0-2 oxygen and 0-2 sulfur, the ring system optionally substituted with at least one member independently selected from W;

R⁹ is selected from the group phenyl and pyridyl, each optionally substituted with at least one member independently selected from W; and

W is selected from the group halogen, cyano, formyl, nitro, SF₅, C₁-C₃ alkyl, C₁-C₃ haloalkyl, C₁-C₃ alkylthio, C₁-C₃ alkoxy, C₁-C₃ haloalkoxy, C₂-C₄ alkylcarbonyl and C₂-C₄ alkoxycarbonyl.

The oxazoline and thiazoline compounds of the present invention are not disclosed in any of these publications.

SUMMARY OF THE INVENTION

This invention is directed to compounds of Formula I including all geometric and stereoisomers, N-oxides, and agriculturally suitable salts thereof, agricultural compositions containing them and their use as arthropodicides:

wherein:

each E is independently selected from the group C₁-C₄ alkyl and C₁-C₄ haloalkyl;

X is selected from the group C₁-C₄ alkylene, -(CH₂)_n-A-, -(CH₂)_p-A-CH₂-, each group optionally substituted with one to four R⁴;

Y and Z are independently selected from the group O and S;

A is selected from the group O, S and ΝR¹⁰;

Q is selected from the group H and J; or Q is selected from the group C₁-C₁₆

alkyl, C₁-C₁₆ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₇ cycloalkyl, C₃-C₇ halocycloalkyl and C₄-C₇ cycloalkylalkyl, each group optionally substituted with W;

J is selected from the group phenyl, naphthalenyl, anthracenyl, phenanthrenyl, 1H-pyrrolyl, furanyl, thienyl, 1H-pyrazolyl, 1H-imidazolyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, 1H-1,2,3-triazolyl, 2H-1,2,3-triazolyl, 1H-1,2,4-triazolyl, 4H-1,2,4-triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1H-tetrazolyl, 2H-tetrazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, 1,3,5-triazinyl, 1,2,4-triazinyl,

1,2,4,5-tetrazinyl, 1H-indolyl, benzofuranyl, benzo[b]thiophenyl,

1H-indazolyl, 1H-benzimidazolyl, benzoxazolyl, benzothiazolyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl,

1,8-naphthyridinyl, pteridinyl, 2,3-dihydro-1H-indenyl,

1,2,3,4-tetrahydronaphthalenyl, 6,7,8,9-tetrahydro-5H-benzocycloheptenyl, 2,3-dihydrobenzofuranyl, 3,4-dihydro-2H-1-benzopyranyl,

2,3,4,5-tetrahydro-1-benzoxepinyl, 1,3-benzodioxolyl,

1,3-dihydro-1-oxoisobenzofu ranyl ; 2,3-dihydro-2-oxobenzofuranyl, 3,4-dihydro-4-oxo-2H-1-benzopyranyl and 9H-fluorenyl, wherein J is optionally substituted with 1-4 R³;

R¹ is selected from the group 1 -2 halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, S(O)_tR¹¹ , cyano and nitro;

R² is selected from the group Η, 1-2 halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl. C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, S(O)_tR^{1 1}, cyano and nitro;

each R³ is independently selected from the group halogen, C₁-C₁₆ alkyl, C₁-C₁₆, haloalkyl, C₂-C₁₆ alkenyl, C₂-C₁₆ haloalkenyl, C₂-C₁₆ alkynyl, C₂-C₁₆ haloalkynyl, C₂-C₁₆ alkoxyalkyl, C₂-C₁₆ alkylthioalkyl, C₂-C₁₆ cyanoalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, cyano, nitro, S(O)_tR¹¹ , OR⁹, C₁-C₅ alkyldithio, C₁-C₅ haloalkyldithio, formyl, C(O)R²¹, C(O)OR²¹,

C(O)NR¹²R¹³, S(O)₂NR¹⁴R¹⁵, NR¹⁶R¹⁷, Si(R⁶)(R⁷)(R⁸), SF₅ and M-J¹; each R⁴ is independently selected from the group C₁-C₄ alkyl, C₁-C₄ haloalkyl,

C₂-C₄ cyanoalkyl, C₂-C₄ alkoxyalkyl, and phenyl optionally substituted with 1-3 W¹; or two R⁴ bonded to the same carbon atom can be taken together with the carbon to which they are attached to form C(=O) or C(=S);

R⁵ is selected from the group Η, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl and C₁-C₆ haloalkylsulfonyl;

each R⁶ and R⁷ is independently C₁-C₁₂ alkyl;

each R⁸ is independently selected from the group C₁-C₁₂ alkyl and phenyl

optionally substituted with 1-3 W¹;

each R⁹ is independently selected from the group H, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₄-C₇ cyanocycloalkyl, C₄-C₇

alkylcycloalkyl, C₄-C₇ cycloalkylalkyl, C₄-C₇ halocycloalkylalkyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₂-C₄ cyanoalkyl, C(O)R¹⁸, C(O)OR¹⁸,

C(O)NR¹²R¹³, S(O)₂NR¹⁴R¹⁵ and S(O)₂R¹¹ ;

R¹⁰ is selected from the group H, C₁-C₄ alkyl, C₁-C₄ haloalkyl, formyl, C₂-C₄ alkylcarbonyl, C₂-C₄ alkoxycarbonyl, NH₂C(O), (C₁-C₄ alkyl)NHC(O) and (C₁- C₄ alkyl)₂NC(O);

each R¹¹ is independently selected from the group C₁-C₆ alkyl, C₁-C₆ haloalkyl,

C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₄-C₇ cyanocycloalkyl, C₄-C₇

alkylcycloalkyl, C₄-C₇ cycloalkylalkyl, C₄-C₇ halocycloalkylalkyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₂-C₄ cyanoalkyl, phenyl optionally substituted with 1-3 W¹ and benzyl optionally substituted with 1-3 W¹ ; each R¹², R¹⁴ and R¹⁶ is independently selected from the group H, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₄-C₇ cycloalkylalkyl, phenyl optionally substituted with 1-3 W¹ and benzyl optionally substituted with 1-3 W¹ ;

each R¹³, R¹⁵ and R¹⁷ is independently selected from the group H, C₁-C₄ alkyl and C₁-C₄ alkoxy; or

R¹² and R¹³, R¹⁴ and R¹⁵, or R¹⁶ and R¹⁷, when attached to the same atom, can be taken together as (CH₂)₄, (CH₂)₅ or CH₂CH₂OCH₂CH₂, each group optionally substituted with 1-3 CH₃;

each R¹⁸ is independently selected from the group C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₃- C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₄-C₇ cycloalkylalkyl, phenyl optionally substituted with 1-3 W¹ and benzyl optionally substituted with 1-3 W¹; each R¹⁹ is independently selected from the group halogen, cyano, nitro, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₄ cyanoalkyl, S(O)_tR¹¹ , OR²⁰, C₁-C₅ alkyldithio, C₁-C₅

haloalkyldithio, SF₅, formyl, C(O)R¹⁸, C(O)OR¹⁸ and Si(R⁶)(R⁷)(R⁸); each R²⁰ is independently selected from the group H, C₁-C₆ alkyl, C₁-C₆

haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C(O)R¹⁸, C(O)OR¹⁸, C(O)NR¹²R¹³, S(O)₂NR¹⁴R¹⁵, S(O)₂R^{1 1}, phenyl optionally substituted with 1-3 W¹ and benzyl optionally substituted with 1-3 W¹;

each R²¹ is independently selected from the group C₁ -C₆ alkyl, C₁ -C₆ haloalkyl,

C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₄-C₇ cycloalkylalkyl;

each M is independently selected from the group direct bond, S, O, C(O), C₁-C₄ alkylene, C₂-C₄ alkenylene and C₂-C₄ alkynylene;

each J¹ is independently selected from the group Si(R²²)(R²³)(R²⁴);

Ge(R²²)(R²³)(R²⁴); 2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecan-1-yl optionally substituted with 1-6 C₁-C₃ alkyl; C₁-C₆ alkyl substituted with 1-3 C₁-C₄ alkoxy; and phenyl, naphthalenyl and pyridyl, each optionally substituted with 1-4 R¹⁹;

each R²² and R²³ is independently selected from the group C₁-C₁₂ alkyl and

C₁-C₁₂ alkoxy;

each R²⁴ is independently selected from the group C₁-C₁₂ alkyl; C₁-C₁₂ alkoxy; and phenyl optionally substituted with 1-3 W¹;

W is selected from the group J, C₁-C₆ alkoxy and C₁-C₆ haloalkoxy;

each W¹ is independently selected from the group halogen, cyano, nitro, C₁-C₂ alkyl, C₁-C₂ haloalkyl, C₁-C₂ alkoxy, C₁-C₂ haloalkoxy, C₁-C₂ alkylthio, C₁-C₂ haloalkylthio, C₁-C₂ alkylsulfinyl, C₁-C₂ haloalkylsulfinyl, C₁-C₂ alkylsulfonyl and C₁-C₂ haloalkylsulfonyl;

m is 1 or 2;

n is 1, 2 or 3;

p is 1 or 2;

q is 0, 1 or 2; and

each t is independently 0, 1 or 2.

In the above recitations, the term "alkyl", used either alone or in compound words such as "alkylthio" or "haloalkyl" includes straight-chain or branched alkyl, such as, methyl, ethyl, n-propyl, i-propyl, or the different butyl, pentyl or hexyl isomers. The term "1-6 alkyl" indicates that one to six of the available positions for that substituent may be alkyl which are independently selected. "Alkenyl" includes straight-chain or branched alkenes such as vinyl, 1-propenyl, 2-propenyl, and the different butenyl, pentenyl and hexenyl isomers. "Alkenyl" also includes polyenes such as 1,2-propadienyl and 2,4-hexadienyl. "Alkynyl" includes straight-chain or branched alkynes such as ethynyl, 1-propynyl, 2-propynyl and the different butynyl, pentynyl and hexynyl isomers. "Alkynyl" can also include moieties comprised of multiple triple bonds such as

2,5-hexadiynyl. "Alkylene" denotes a straight-chain or branched alkanediyl. Examples of "alkylene" include CH₂, CH₂CH₂, CH(CH₃), CH₂CH₂CH₂, CH₂CH(CH₃) and the different butylene isomers. "Alkenylene" denotes a straight-chain or branched alkenediyl containing one olefinic bond. Examples of "alkenylene" include CH=CH, CH₂CH=CH, CH=C(CH₃) and the different butenylene isomers. "Alkynylene" denotes a straight-chain or branched alkynediyl containing one triple bond. Examples of "alkynylene" include C≡C, CH₂C≡C, C≡CCH₂ and the different butynylene isomers. "Alkoxy" includes, for example, methoxy, ethoxy, n-propyloxy, isopropyloxy and the different butoxy, pentoxy and hexyloxy isomers. The term "1-3 alkoxy" indicates that one to three of the available positions for that substituent may be alkoxy which are independently selected.

"Alkoxyalkyl" denotes alkoxy substitution on alkyl. Examples of "alkoxyalkyl" include CH₃OCH₂, CH₃OCH₂CH₂, CH₃CH₂OCH₂, CH₃CH₂CH₂CH₂OCH₂ and

CH₃CH₂OCH₂CH₂. "Alkylthio" includes branched or straight-chain alkylthio moieties such as methylthio, ethylthio, and the different propylthio, butylthio, pentylthio and hexylthio isomers. "Alkylthioalkyl" denotes alkylthio substitution on alkyl. Examples of "alkylthioalkyl" include CH₃SCH₂, CH₃SCH₂CH₂, CH₃CH₂SCH₂,

CH₃CH₂CH₂CH₂SCH₂ and CH₃CH₂SCH₂CH₂. "Alkylsulfinyl" includes both enantiomers of an alkylsulfinyl group. Examples of "alkylsulfinyl" include CH₃S(O), CH₃CH₂S(O), CH₃CH₂CH₂S(O), (CH₃)₂CHS(O) and the different butylsulfinyl, pentylsulfinyl and hexylsulfinyl isomers. Examples of "alkylsulfonyl" include CH₃S(O)₂, CH₃CH₂S(O)₂, CH₃CH₂CH₂S(O)₂, (CH₃)₂CHS(O)₂ and the different butylsulfonyl, pentylsulfonyl and hexylsulfonyl isomers. "Alkyldithio" denotes branched or

straight-chain alkyldithio moieties. Examples of "alkyldithio" include CH₃SS,

CH₃CH₂SS, CH₃CH₂CH₂SS, (CH₃)₂CHSS and the different butyldithio and

pentyldithio isomers. "Cyanoalkyl" denotes an alkyl group substituted with one cyano group. Examples of "cyanoalkyl" include NCCH₂, NCCH₂CH₂ and CH₃CH(CN)CH₂. "Cycloalkyl" includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. Examples of "cycloalkylalkyl" include cyclopropylmethyl, cyclopentylethyl, and other cycloalkyl moieties bonded to straight-chain or branched alkyl groups. "Alkylcycloalkyl" denotes alkyl substitution on a cycloalkyl moiety. Examples include 4-methylcyclohexyl and 3-ethylcyclopentyl. "Cyanocycloalkyl" denotes a cycloalkyl group substituted with one cyano group. Examples of "cyanocycloalkyl" include 4-cyanocyclohexyl and 3-cyanocyclopentyl. One skilled in the art will appreciate that not all nitrogen containing heterocycles can form N-oxides since the nitrogen requires an available lone pair for oxidation to the oxide; one skilled in the art will recognize those nitrogen containing heterocycles which can form N-oxides.

The term "halogen", either alone or in compound words such as "haloalkyl", includes fluorine, chlorine, bromine or iodine. The term "1-2 halogen" indicates that one or two of the available positions for that substituent may be halogen which are independently selected. Further, when used in compound words such as "haloalkyl", said alkyl may be partially or fully substituted with halogen atoms which may be the same or different. Examples of "haloalkyl" include F₃C, ClCH₂, CF₃CH₂ and CF₃CCl₂. The terms "haloalkenyl", "haloalkynyl", "haloalkoxy", and the like, are defined analogously to the term "haloalkyl". Examples of "haloalkenyl" include (Cl)₂C=CHCH₂ and

CF₃CH₂CH=CHCH₂. Examples of "haloalkynyl" include HC≡CCHCl, CF₃OC, CCl₃C≡C and FCH₂C≡CCH₂. Examples of "haloalkoxy" include CF₃O, CCl₃CH₂O, HCF₂CH₂CH₂O and CF₃CH₂O. Examples of "haloalkylthio" include CC1₃S, CF₃S, CCl₃CH₂S and ClCH₂CH₂CH₂S. Examples of "haloalkylsulfonyl" include CF₃S(O)₂, CCl₃S(O)₂, CF₃CH₂S(O)₂ and CF₃CF₂S(O)₂.

The total number of carbon atoms in a substituent group is indicated by the "C_i-C_j" prefix where i and j are numbers from 1 to 16. For example, C₁-C₃ alkylsulfonyl designates methylsulfonyl through propylsulfonyl; C₂ alkoxyalkyl designates CH₃OCH₂: C₃ alkoxyalkyl designates, for example, CH₃CH(OCH₃), CH₃OCH₂CH₂ or

CH₃CH₂OCH₂; and C₄ alkoxyalkyl designates the various isomers of an alkyl group substituted with an alkoxy group containing a total of four carbon atoms, examples including CH₃CH₂CH₂OCH₂ and CH₃CH₂OCH₂CH₂. Examples of "alkylcarbonyl" include C(O)CH₃, C(O)CH₂CH₂CH₃ and C(O)CH(CH₃)₂. Examples of

"alkoxycarbonyl" include CH₃OC(=O), CH₃CH₂OC(=O), CH₃CH₂CH₂OC(=O),

(CH₃)₂CHOC(=O) and the different butoxycarbonyl isomers. In the above recitations, when a compound of Formula I is comprised of one or more heterocyclic rings, all substituents are attached to these rings through any available carbon or nitrogen by replacement of a hydrogen on said carbon or nitrogen.

The term "2,8,9-trioxa-5-aza-1-silabicyclo[3.3.3]undecan-1-yl" designates the silyl radical:

When a compound is substituted with a substituent bearing a subscript that indicates the number of said substituents can exceed 1 , said substituents (when they exceed 1) are independently selected from the group of defined substituents.

When a group contains a substituent which can be hydrogen, for example R² or

R¹⁰, then, when this substituent is taken as hydrogen, it is recognized that this is equivalent to said group being unsubstituted.

Compounds of this invention can exist as one or more stereoisomers. The various stereoisomers include enantiomers, diastereomers, atropisomers and geometric isomers. One skilled in the art will appreciate that one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate, enrich, and/or to selectively prepare said stereoisomers. Accordingly, the present invention comprises compounds selected from Formula I, N-oxides and agriculturally suitable salts thereof. The compounds of the invention may be present as a mixture of stereoisomers, individual stereoisomers, or as an optically active form.

The salts of the compounds of the invention include acid-addition salts with inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids. The salts of the compounds of the invention also include those formed with organic bases (e.g., pyridine, ammonia, or triethylamine) or inorganic bases (e.g., hydrides, hydroxides, or carbonates of sodium, potassium, lithium, calcium, magnesium or barium) when the compound contains an acidic group such as a phenol.

Preferred compounds for reasons of better activity and/or ease of synthesis are:

Preferred 1. Compounds of Formula I above, and N-oxides and

agriculturally-suitable salts thereof, wherein:

X is -(CH₂)_n-A- optionally substituted with one to four R⁴; Y is O;

A is O;

Q is selected from the group J and C₁-C₁₆ alkyl;

J is selected from the group phenyl, thienyl and pyridinyl, each optionally substituted with 1-3 R³;

m is 1 ; and n is 1.

Preferred 2. Compounds of Preferred 1 wherein:

Z is O;

Q is J;

J is selected from the group phenyl and pyridinyl, each optionally

substituted with 1-3 R³; and

q is O.

Preferred 3. Compounds of Preferred 2 wherein:

R¹ is selected from the group F and Cl in the 2-position;

R² is selected from the group H, F and Cl in the 6-position; each R³ is independently selected from the group halogen, C₁-C₆ alkyl,

C₁-C₆ haloalkyl, S(O)_tR^{1 1}, OR⁹ and M-J¹;

each R⁹ is independently selected from the group C₁-C₄ alkyl and C₁-C₄ haloalkyl;

each R¹¹ is independently selected from the group C₁ -C₆ alkyl and C₁-C₆ haloalkyl; and

each J¹ is independently selected from the group phenyl, thienyl, pyridinyl and furanyl.

Most preferred are compounds of Preferred 3 selected from the group:

(Z)-5-[(4-chlorophenyl)methylene]-3-[2-(2,6-difluorophenyl)-4,5-dihydro-4- oxazolyl]-4-oxazolidinone;

(Z)-3-[2-(2,6-difluorophenyl)-4,5-dihydro-4-oxazolyl]-5-[[4- (trifluoromethyl)phenyl]methylene]-4-oxazolidinone;

(Z)-5-[(4^,-chloro[1,1'-biphenyl]-4-yl)methylene]-3-[2-(2,6-difluorophenyl)-4,5- dihydro-4-oxazolyl]-4-oxazolidinone;

(Z)-3-[2-(2,6-difluorophenyl)-4,5-dihydro-4-oxazolyl]-5-[(4'-fluoro[1,1'- biphenyl]-4-yl)methylene]-4-oxazolidinone; and

(Z)-5-[(2',4^,-dichloro[1,1'-biphenyl]-4-yl)methylene]-3-[2-(2,6-difluorophenyl)- 4,5-dihydro-4-oxazolyl]-4-oxazolidinone.

This invention also relates to arthropodicidal compositions comprising

arthropodicidally effective amounts of the compounds of the invention and at least one of a surfactant, a solid diluent or a liquid diluent. The preferred compositions of the present invention are those which comprise the above preferred compounds.

This invention also relates to a method for controlling arthropods comprising contacting the arthropods or their environment with an arthropodicidally effective amount of the compounds of the invention (e.g., as a composition described herein). The preferred methods of use are those involving the above preferred compounds.

DETAILS OF THE INVENTION

The compounds of Formula I can be prepared by one or more of the following methods and variations as described in Schemes 1-14. The definitions of E, X, Y, Z, A, Q, J, R¹-R²⁴, M, J¹, W, W¹, m, n, p, q and t in the compounds of Formulae I-XIX below are as defined above in the Summary of the Invention.

Compounds of Formula I (R⁵ = H, X = -C(R^4a)₂A-) can be prepared by the reaction of a Formula II compound with a Formula HI compound in the presence of a base such as sodium hydride or lithium diisopropylamide (Scheme 1). The reaction may be run in the presence or absence of a solvent such as tetrahydrofuran (THF), dimethylformamide (DMF), ether, benzene or toluene. The reaction temperature can vary from 0°C to the boiling point of the solvent being used and is usually completed in less than 24 h.

Compounds of Formula II (Y = S) may be prepared by thionation of a Formula II compound (Y = O) with 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4- disulfide (Lawesson's Reagent). Thionation reactions have been thoroughly reviewed by

M. Cava and M. Levinson in Tetrahedron (1987), 41, 5061-5087. This transformation is shown in Scheme 2.

Formula II compounds (Y = O) can be prepared by a condensation reaction between a propiolic acid of Formula IV (V = OH) and an amine of Formula V in the presence of a coupling agent such as dicyclohexylcarbodiimide (DCC). Typically, the reaction involves mixing a Formula IV compound (V = OH) with an equimolar amount of a Formula V compound in a suitable solvent such as methylene chloride, ethyl acetate or DMF and adding a slight excess of DCC. The reaction temperature can vary from 0-150°C. (A review of DCC coupling reactions can be found in Tetrahedron (1981), 37, 233). Alternatively, the condensation reaction can be performed with an acid chloride of Formula IV (V = Cl) and a Formula V compound in the presence of an acid scavenger (usually a tertiary amine base such as triethylamine) at room temperature or below. The reaction can be carried out in an inert solvent as methylene chloride, chloroform, benzene, tetrahydrofuran, toluene or other solvents that will not react with acid chlorides or bases. The reaction is normally completed in less than 24 h. (See Scheme 3). Other useful methods for the formation of amides are discussed in Larock, Comprehensive Organic Transformations, VCH Publishers, Inc., New York.

Scheme 4 illustrates the preparation of Formula IV compounds. An acrylate of Formula VI is brominated with bromine in an inert solvent such as methylene chloride, carbon tetrachloride, chloroform or ether followed by dehydrobromination of the dibromo intermediate with a base such as sodium hydroxide or potassium hydroxide. The reaction may be run in a solvent such as methanol, ethanol, water or DMF. An example of this transformation can be found in Organic Synthesis, Coll. Vol. II, p 270. Alternative methods of making compounds of Formula IV (V = OH) have been described by Chenault and Dupin in Synthesis (1987), 498, by Yamanaka et al. in Synthesis (1992), 746 and by Hendrickson and Hussoin in Synthesis (1989), 217. A Formula IV compound (V = OH) can further be transformed into a Formula IV compound (V = Cl) using conventional methods of converting a carboxylic acid into an acid chloride. (See Larock, Comprehensive Organic Transformations, VCH Publishers, Inc., New York).

Compounds of Formula VI (L = Me, Et) can be prepared by the reaction of aldehydes of Formula VII with phosphonium salts of Formula VIII (L = Me, Et) in the presence of a strong base. Aldehydes of Formula VII and phosphonium salts of Formula VIII are commercially available or can be prepared by known methods. A typical reaction involves mixing a Formula VIII compound with a strong base such as an alkyllithium (e.g., butyllithium), a metal alkoxide (e.g., sodium methoxide), sodium amide or sodium hydride in a suitable solvent such as tetrahydrofuran, ether, benzene, methanol, toluene, acetonitrile, dimethoxyethane and dimethyl sulfoxide, followed by addition of an aldehyde of Formula VII. The temperature of the reaction can vary from

-70-200°C with a preferred temperature range of 0-100°C. The Wittig reaction has been reviewed by Maercker in Organic Reactions (1965), 14, 270-490. The transformation is illustrated in Scheme 5.

, .

Alternatively, compounds of Formula I can be prepared by an aldol-type condensation of a Formula IX compound with an aldehyde of Formula VII. Scheme 6 illustrates this transformation. The reaction can be run in the presence of a base such as a metal alkoxide, e.g., sodium methoxide, or an amine base as piperidine or

1,4-diazabicyclo[2.2.2]octane (DABCO). A suitable solvent for this transformation can be chosen from, but not limited to, methanol, ethanol, water, xylene, DMF, dioxane or THF. The reaction temperature can vary from 0-200°C and the reaction is done in less than 48 h. An example of this reaction can be found in Organic Synthesis, Coll. Vol. 5, (1973), p 627.

Scheme 7 shows the preparation of compounds of Formula IX (where

X = -A(CH₂)_n-). The reaction involves the cyclization of a Formula X compound with a compound of Formula XI in the presence of a base. Compounds of Formula XI are commercially available or can be prepared by known methods. Examples of bases that can be used include sodium hydride or potassium t-Bu toxide. The reaction may be run in a solvent such as benzene, THF, ether, toluene, DMF, dimethyl sulfoxide (DMSO) or dioxane. The reaction temperature may vary from 0-200°C and the reaction is usually done within 24 h.

Compounds of Formula X (Y = O) can be prepared by reaction of a carboxylic acid of Formula XII with an amine of Formula V. Compounds of Formula XII are commercially available or can be prepared by known methods. The reaction conditions are as described for Scheme 3.

Compounds of Formula IX (where X is -CH₂(CH₂)_n-) can be prepared by cyclization of a bromide of Formula XIII in the presence of a base as shown in Scheme 9. Reaction conditions are similar to those of Scheme 7.

Scheme 10 illustrates the synthesis of compounds of Formula XIII. The reaction involves the coupling of an acid of Formula XIV with an amine of Formula V as described for Scheme 3.

Compounds of Formula V can be prepared by the reaction of compounds of Formula XV with sodium hypobromite (or sodium hydroxide and bromine). This transformation is shown in Scheme 11. A review of the Hofmann rearrangement can be found in Organic Reactions (1946), 3, 267-306. A typical reaction involves the addition of a compound of Formula XIII to an aqueous solution of sodium hypobromite. The temperature of the reaction can range from 0-200°C with the preferred temperature range between 30-100°C. The reaction is usually complete in 24 h. Alternatively, the transformation can be accomplished by treating a Formula XV compound with

[hydroxy(tosyloxy)iodo]benzene in refluxing acetonitrile. (See J. Org. Chem. (1986), 51, 2669-2671).

Compounds of Formula XV can be prepared by reacting compounds of

Formula XVI with ammonia. This transformation is shown in Scheme 12. The reaction can be run in solvents such as methanol, ethanol, ether, benzene and toluene. Typical reactions are carried out at ambient temperature, and reactions are usually completed in 24 h. For reference, see D. W. Jones, J. Chem. Soc. (1969), 1729.

Compounds of Formula XVI can be prepared by the reaction of serine derivatives (Formula XVII) with an imidate of Formula XVIII as shown in Scheme 13. Serine derivatives of Formula XVIII are commercially available or can be prepared by known methods. The reaction can be carried out in solvents such as methanol, methylene chloride, chloroform, benzene, dioxane and tetrahydrofuran. Water can be added as a cosolvent. The reaction can be carried out at temperatures varying from 0°C to the reflux temperature of the particular solvent being used, and the reaction is usually complete in 24 h. For reference, see Agric. Biol. Chem. (1986), 50, 615-623.

As depicted in Scheme 14, imidates of Formula XVI can be prepared from amides of Formula XVII by reaction with a trialkyloxonium tetrafluoroborate in an inert solvent such as methylene chloride, benzene or toluene. Amides of Formula XVII are commercially available or can be prepared by known methods. The syntheses of imidates has been extensively reviewed by D. A. Neilson in The Chemistry of Amidines and Imidates, Patai and Rappoport, Eds., Vol. 2, (1991), pp 425-483.

It is recognized that some reagents and reaction conditions described above for preparing compounds of Formula I may not be compatible with certain functionalities present in the intermediates. In these instances, the incorporation of

protection/deprotection sequences or functional group interconversions into the synthesis will aid in obtaining the desired products. The use and choice of the protecting groups will be apparent to one skilled in chemical synthesis (see, for example, Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 2nd ed.; Wiley: New York, 1991). One skilled in the art will recognize that, in some cases, after the introduction of a given reagent as it is depicted in any individual scheme, it may be necessary to perform additional routine synthetic steps not described in detail to complete the synthesis of compounds of Formula I. One skilled in the art will also recognize that it may be necessary to perform a combination of the steps illustrated in Schemes 1-? in an order other than that implied by the particular sequence presented to prepare the compounds of Formula I. One skilled in the art will also recognize that compounds of Formula I and the intermediates described herein can be subjected to various electrophilic, nucleophilic, radical, organometallic, oxidation, and reduction reactions to add substituents or modify existing substituents.

Without further elaboration, it is believed that one skilled in the art using the preceding description can utilize the present invention to its fullest extent. The following Examples are, therefore, to be construed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Percentages are by weight except for

chromatographic solvent mixtures or where otherwise indicated. Parts and percentages for chromatographic solvent mixtures are by volume unless otherwise indicated.

1H NMR spectra are reported in ppm downfield from tetramethylsilane; s = singlet, d = doublet, t = triplet, q = quartet, ABq = "AB" quartet, m = multiplet, dd = doublet of doublets, br s = broad singlet.

EXAMPLE 1

Step A: Methyl 2,6-difluorobenzenecarboximidate

An amount of 10.62 g (0.068 mol) of 2,6-difluorobenzamide was added to a suspension of 10.0 g (0.068 mol) of trimethyloxonium tetrafluoroborate in 70 mL of methylene chloride. The reaction was stirred under nitrogen overnight. Saturated aqueous sodium bicarbonate was slowly added and the mixture was extracted with methylene chloride. The combined extracts were washed with brine, dried over MgSO₄ and evaporated. The residue was passed through a silica gel column eluting with EtOAc:hexane (1:6) to give 9.13 g of the title compound of Step A as a pale yellow oil. ¹H NMR (CDCl₃): δ 7.70 (br s.1H), 7.73 (m,1H). 6.94 (t,2H). 3.94 (s,3H).

Step B: Methyl 2-(2,6-difluorophenyl)-4,5-dihydro-4-oxazolecarboxylate

An amount of 9.09 g (0.058 mol) of serine methyl ester hydrochloride was added portionwise to a 10.0 g (0.058 mol) solution of the title compound of Step A in 15 mL EtOH and 5 mL H₂O. The mixture was stirred at reflux for 1.5 h. Volatiles were evaporated under reduced pressure and the residue was partitioned between ethyl acetate (EtOAc) and H₂O. The EtOAc layer was washed with brine, dried over MgSO₄ and evaporated. The residue was passed through a silica gel column eluting with

EtOAc:hexane (1:4) to give 6.0 g of the title compound of Step B as a colorless oil.

¹H NMR (CDCl₃): δ 7.43 (m,1H), 6.98 (t,2H) 5.00 (t,1H), 4.63-4.72 (2t,2H), 3.84

(s,3H).

Step C: 2-(2,6-Difluorophenyl)-4,5-dihydro-4-oxazolecarboxamide

A solution of 10.0 g (0.041 mol) of the title compound of Step B in 100 mL of a

2M solution of ammonia in MeOH was stirred at room temperature overnight. Evaporation of the solvent afforded 9.04 g of the title compound of Step C as a white powder melting at 148-149°C. ¹H NMR (Me₂SO-d₆): δ 7.67 (m,1H), 7.49 (br s,1H), 7.39 (br s,1H), 7.27 (t,2H), 4.85 (t,1H), 4.56 (2t,2H).

Step D: 2-(2,6-Difluorophenyl)-4,5-dihydro-4-oxazolamine

An amount of 0.386 g (0.0044 mol) of bromine was added dropwise to a cooled solution of 0.440 g (0.011 mol) of NaOH in 3.7 mL of H₂O. 0.500 g (0.002 mol) of the title compound of Step C was added portionwise. The reaction was stirred at 80°C for 0.5 h. Et₂O and H₂O were added and the mixture was extracted with EtOAc. The combined extracts were washed with brine, dried over MgSO₄ and evaporated to give 0.350 g of the title compound of Step D as a white solid melting at 81-85°C. ¹H NMR (Me₂SO-d ₆): δ 7.62 (m,1H), 7.24 (t,2H), 5.15 (t,1H), 4.70 (t.1H), 3.83 (t,1H).

Step E: 3-(4-Chlorophenyl)- N-[2-(2,6-difluorophenyl)-4,5-dihydro-4-oxazolyl]-2- propynamide

1,3-Dicyclohexylcarbodiimide (1.03 g, 0.005 mol) was added portionwise to a cooled (ice-bath) mixture of the title compound of Step D (0.991 g, 0.005 mol),

4-dimethylaminopyridine (0.061 g, 0.0005 mol) and 3-(4-chlorophenyl)propiolic acid (0.963 g, 0.005 mol) in 18 mL of methylene chloride. The mixture was stirred at room temperature for 0.5 h and then the solids were filtered off. The filtrate was evaporated and the residue was passed through a silica gel column eluting with EtOAc :hexanes (1:3) to give 1.66 g of the title compound of Step E as a yellow solid melting at 134- 135°C. ¹H ΝMR (CDCl₃): δ 4.35 (dd,1H), 4.70 (t,1H), 6.20 (m.1H), 6.51 (d.1H), 7.00 (t,2H), 7.35 (m,2H), 7.45 (m,3H).

Step F: (Z)-5-[(4-Chlorophenynmethylenel-3-[2-[2,6-difluorophenyn-4,5- dihydro-4-oxazolyl]-4-oxazolidinone

Sodium hydride (60% dispersion in oil, 0.088 g, 0.0022 mol) was added to a cooled (ice-bath) mixture of the title compound of Step E (0.731 g, 0.002 mol) and paraformaldehyde (0.300 g, 0.01 mol) in 2 mL of dry DMF. The mixture was stirred in the cold for 0.5 h and then was carefully quenched with water while cooling. The resulting mixture was extracted with EtOAc and the combined extracts were washed with water. The organic layer was dried (MgSO₄) and evaporated to give a yellow solid which, upon trituration with ether/hexanes, afforded 0.432 g of the title compound of Step F, a compound of the invention, as a white solid melting at 131 - 134°C. ¹H ΝMR (CDCl₃): δ 4.25 (dd.1H), 4.70 (t,1H), 5.48 (ABq,2H), 6.28 (s,1H), 6.50 (dd.1H), 7.00 (t,2H), 7.35 (d,2H), 7.50 (m,1H), 7.60 (d,2H). EXAMPLE 2

Step A: Methyl 3-(4-iodophenyl)-2-propenoate

An amount of 5.0 g (0.0215 mol) of 4-iodobenzaldehyde was dissolved in 22 mL of acetonitrile. Methyl(triphenylphosphoranylidene) acetate (14.41 g, 0.043 mol) was added and the mixture was refluxed overnight. The reaction was quenched with 1N HCl and extracted three times with EtOAc. The combined extracts were washed with water, dried (MgSO₄) and evaporated. The residue was passed through a silica gel column eluting with EtOAc:hexanes (1: 10) to give 5.60 g of the title compound of Step A as an oil. ¹H-NMR (CDCl₃): δ 3.805 (s,3H), 6.439 (d,1H), 7.228 (d,2H), 7.629 (d,1H), 7.712 (d,2H).

Step B: 3-(4-Iodophenyl)-2-propynoic acid

5.60 g (0.019 mol) of the title compound of Step A was dissolved in 19 mL of methylene chloride. The mixture was cooled to 0°C and bromine (0.97 mL) was added dropwise. The reaction was stirred at room temperature for 1 h and the solvents were evaporated. The residue was added to a solution of 4.78 g of KOH in 23 mL of EtOH at 50°C. This mixture was refluxed for 18 h. The solvents were evaporated and the solid was dissolved in water. Insoluble material was filtered and the pH of the solution was adjusted to 2 using HCl. The resulting precipitate was filtered to give 4.7 g of the title compound of Step B as an off-white solid melting at 180-184°C. ¹H-NMR (DMSO-d₆): δ 7.390 (d,2H), 7.50 (d,2H).

Step C: N-[2-(2,6-Difluorophenyl)-4,5-dihydro-4-oxazolyl]-3-(4-iodophenyl)-2- propynamide

To a cooled (0°C) solution of 0.680 g (0.0025 mol) of the title compound of Step B in 7 mL CH₂Cl₂ was added 0.533 g (0.0025 mol) of

1,3-dicyclohexylcarbodiimide, 0.032 g of 4-dimethylaminopyridine and 0.500 g of the title compound of Step D in Example 1. The reaction mixture was stirred at room temperature for 30 minutes and the solids were filtered off. Evaporation of the solvents from the filtrate produced a residue which was passed through a silica gel column eluting with EtOAc:hexanes ( 1 : 1 ) to give 0.960 g of the title compound of Step C as a solid melting at 150-152°C. ¹H-ΝMR (CDCl₃): δ 4.340 (m,1H), 4.691 (t,1H), 6.204 (m.1H), 7.200 (m,3H), 7.205 (d,2H), 7.449 (m,1H), 7.684 (d,2H).

Step D: (Z)3-[2-(2,6-Difluorophenyl)-4,5-dihydro-4-oxazolyl]-5-[(4- iodophenyl)methylene]-4-oxazolidinone

Sodium hydride (60% dispersion in oil, 0.044 g, 0.0011 mol) was added to a cooled (ice-bath) mixture of the title compound of Step C (0.452 g, 0.001 mol) and paraformaldehyde (0.148 g, 0.005 mol) in 1 mL of dry DMF. The mixture was stirred in the cold for 1 hour and was then carefully quenched with water in the cold. The resulting mixture was extracted with EtOAc and the combined extracts were washed with water. The organic layer was dried (MgSO₄) and evaporated. The residue was passed through a silica gel column eluting with EtOAc:h exane (1:2) to give 0.170 g of the title compound of Step D, a compound of the invention, as an oil which solidified on standing to a solid melting at 165-167°C. ¹H-NMR (CDCl₃): δ 4.471 (q.1H), 4.679 (t,1H), 5.439 (d,1H), 5.516 (d,1H), 6.237 (s,1H), 6.507 (m,1H), 7.026 (t,2H), 7.381 (m,2H), 7.505 (m,1H), 7.683 (m,2H).

EXAMPLE 3

(Z)-5-[(2',4'-Dichloro[1,1'-biphenyl]-4-yl)methylenel-3-[2-(2,6-difluorophenyl)-4,5- dihydro-4-oxazolyl]-4-oxazolidinone

An amount of the title compound of Step D in Example 2 (0.482 g, 0.001 mol) was dissolved in 2 mL of dimethoxyethane. To this solution was added 1.04 mL of 2M Na₂CO₃, 0.036 g (0.00003 mol) of tetrakis(triphenylphosphine)palladium(0) and 0.191 g (0.001 mol) of 2,4-dichlorobenzeneboronic acid in 0.53 mL of MeOH. The reaction was stirred at 80°C overnight and then was quenched with 9.75 mL of a 2M Na₂CO₃ solution containing 0.78 mL of 30% NH₄OH. The mixture was extracted with methylene chloride and the organic extracts were washed with aqueous saturated NaHCO₃. The organic extracts were dried, filtered and evaporated to give a residue which was passed through a silica gel column eluting with EtOAc:hexanes ( 1 :2) to give 0.300 g of the title compound of Example 3, a compound of the invention, as a solid melting at 151-153°C. ¹H-NMR (CDCl₃): δ 4.488 (m, 1H), 4.688 (m, 1H), 5.532 (m,1H), 5.463 (d.1H), 6.370 (s.1H), 6.522 (m.1H). 7.026 (m.2H), 7.285 (m.2H), 7.424 (m,2H), 7.486 (m,2H), 7.719 (m,2H).

EXAMPLE 4

(Z)-3-[2-[2,6-Difluorophenyl)-4,5-dihydro-4-oxazolyl]-5-[[4- [(trimethylsilyl)ethynynphenyllmethylene-4-oxazolidinone An amount of the title compound of Step D in Example 2 (0.482 g, 0.001 mol) was added to 2.3 mL of CH₃CN and 2.3 mL of Et₃N. To this mixture was added (trimethylsilyl)acetylene (0.28 mL, 0.002 mol), bis(triphenylphosphine)palladium(II) chloride (0.035 g, 0.00005 mol) and copper(I) iodide (0.0095 g, 0.00005 mol). The reaction mixture was stirred at room temperature overnight. The solvents were evaporated, water was added to the residue and the resulting mixture was extracted with EtOAc. The EtOAc extract was washed with brine, dried (MgSO₄), filtered and evaporated. The residue was passed through a silica gel column eluting with

EtOAc:hexanes (1:2) to give 0.380 g of a solid melting at 123-124°C. ¹H-NMR (CDCI₃): 0.253 (s,9H), 4.449 (m,1H), 4.674 (m.1H), 5.445 (d,1H), 5.525 (d,1H), 6.288 (s,1H), 6.512 (m,1H), 7.023 (m,2H), 7.445 (m,3H), 7.581 (d,2H).

By the procedures described herein together with methods known in the art, the following compounds of Tables 1 to 7 can be prepared. The following abbreviations are used in the Tables which follow: t = tertiary, s = secondary, n = normal, i = iso, c = cyclo, Me = methyl, Et = ethyl, Pr = propyl, n-Pr = n-propyl, i-Pr = isopropyl, Bu = butyl, n-Bu = n-butyl, i-Bu = i-butyl, s-Bu = s-butyl, t-Bu = t-butyl,

c-C₅H₉ = cyclopentyl, c-C₆H_{1 1} = cyclohexyl, Ph = phenyl, OMe = methoxy,

OEt = ethoxy, OPh = phenoxy, SMe = methylthio, SEt = ethylthio, SPh = phenylthio, N(Me)₂ = dimethylamino, CN = cyano, NO₂ = nitro, COOMe = methoxycarbonyl, CHO = formyl, COMe = methylcarbonyl, COPh = phenylcarbonyl,

SiMe₃ = trimethylsilyl, and SO₂Me = methylsulfonyl.

Formulation / Utility

Compounds of this invention will generally be used as a formulation or composition with an agriculturally suitable carrier comprising at least one of a liquid diluent, a solid diluent or a surfactant. The formulation or composition ingredients are selected to be consistent with the physical properties of the active ingredient, mode of application and environmental factors such as soil type, moisture and temperature. Useful formulations include liquids such as solutions (including emulsifiable

concentrates), suspensions, emulsions (including microemulsions and/or suspoemulsions) and the like which optionally can be thickened into gels. Useful formulations further include solids such as dusts, powders, granules, pellets, tablets, films, and the like which can be water-dispersible ("wettable") or water-soluble. Active ingredient can be

(micro)encapsulated and further formed into a suspension or solid formulation;

alternatively the entire formulation of active ingredient can be encapsulated (or

"overcoated"). Encapsulation can control or delay release of the active ingredient.

Sprayable formulations can be extended in suitable media and used at spray volumes from about one to several hundred liters per hectare. High-strength compositions are primarily used as intermediates for further formulation.

The formulations will typically contain effective amounts of active ingredient, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.

Typical solid diluents are described in Watkins, et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, New Jersey. Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950. McCutcheon's Detergents and Emulsifiers Annual, Allured Publ. Corp., Ridgewood, New Jersey, as well as Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964, list surfactants and recommended uses. All formulations can contain minor amounts of additives to reduce foam, caking, corrosion, microbiological growth and the like, or thickeners to increase viscosity.

Surfactants include, for example, polyethoxylated alcohols, polyethoxylated alkylphenols, polyethoxylated sorbitan fatty acid esters, dialkyl sulfosuccinates, alkyl sulfates, alkylbenzene sulfonates, organosilicones, N,N-dialkyltaurates, lignin sulfonates, naphthalene sulfonate formaldehyde condensates, polycarboxylates, and polyoxyethylene/polyoxypropylene block copolymers. Solid diluents include, for example, clays such as bentonite, montmorillonite, attapulgite and kaolin, starch, sugar, silica, talc, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarbonate, and sodium sulfate. Liquid diluents include, for example, water,

N,N-dimethylformamide, dimethyl sulfoxide, N-alkylpyrrolidone, ethylene glycol, polypropylene glycol, paraffins, alkylbenzenes, alkylnaphthalenes, oils of olive, castor, linseed, tung, sesame, corn, peanut, cotton-seed, soybean, rape-seed and coconut, fatty acid esters, ketones such as cyclohexanone, 2-heptanone, isophorone and 4-hydroxy-4- methyl-2-pentanone, and alcohols such as methanol, cyclohexanol, decanol and tetrahydrofurfuryl alcohol.

Solutions, including emulsifiable concentrates, can be prepared by simply mixing the ingredients. Dusts and powders can be prepared by blending and, usually, grinding as in a hammer mill or fluid-energy mill. Suspensions are usually prepared by wet-milling; see, for example, U.S. 3,060,084. Granules and pellets can be prepared by spraying the active material upon preformed granular carriers or by agglomeration techniques. See Browning, "Agglomeration", Chemical Engineering, December 4, 1967, pp 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and following, and WO 91/13546. Pellets can be prepared as described in

U.S. 4,172,714. Water-dispersible and water-soluble granules can be prepared as taught in U.S. 4, 144,050, U.S. 3,920,442 and DE 3,246,493. Tablets can be prepared as taught in U.S. 5,180,587, U.S. 5,232,701 and U.S. 5,208,030. Films can be prepared as taught in GB 2.095,558 and U.S. 3,299,566.

For further information regarding the art of formulation, see U.S. 3,235,361 , Col. 6, line 16 through Col. 7, line 19 and Examples 10-41 ; U.S. 3,309,192. Col. 5. line 43 through Col. 7, line 62 and Examples 8, 12. 15, 39, 41, 52, 53, 58. 132. 138- 140, 162-164, 166, 167 and 169-182; U.S. 2,891,855, Col. 3, line 66 through Col. 5, line 17 and Examples 1-4; Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, pp 81-96; and Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989.

In the following Examples, all percentages are by weight and all formulations are prepared in conventional ways. Compound numbers refer to compounds in Index Tables A-C.

The compounds of this invention exhibit activity against a wide spectrum of foliar-feeding, fruit-feeding, stem or root feeding, seed-feeding, aquatic and

soil-inhabiting arthropods (term "arthropods" includes insects, mites and nematodes) which are pests of growing and stored agronomic crops, forestry, greenhouse crops, ornamentals, nursery crops, stored food and fiber products, livestock, household, and public and animal health. Those skilled in the art will appreciate that not all compounds are equally effective against all growth stages of all pests. Nevertheless, all of the compounds of this invention display activity against pests that include: eggs, larvae and adults of the Order Lepidoptera; eggs, foliar-feeding, fruit-feeding, root-feeding, seed-feeding larvae and adults of the Order Coleoptera; eggs, immatures and adults of the Orders Hemiptera and Homoptera; eggs, larvae, nymphs and adults of the Order Acari; eggs, immatures and adults of the Orders Thysanoptera, Orthoptera and

Dermaptera; eggs, immatures and adults of the Order Diptera; and eggs, juveniles and adults of the Phylum Nematoda. The compounds of this invention are also active against pests of the Orders Hymenoptera, Isoptera, Siphonaptera, Blattaria, Thysanura and Psocoptera; pests belonging to the Class Arachnida and Phylum Platyhelminthes.

Specifically, the compounds are active against southern corn rootworm (Diabrotica undecimpunctata howardi), aster leafhopper (Mascrosteles fascifrons), boll weevil (Anthonomus grandis), two-spotted spider mite (Tetranychus urticae), fall armyworm (Spodoptera frugiperdα), black bean aphid (Aphis fabae), green peach aphid (Myzus persica), cotton aphid (Aphis gossypii), Russian wheat aphid (Diuraphis noxia), English grain aphid (Sitobion avenae), tobacco budworm (Heliothis virescens), rice water weevil (Lissorhoptrus oryzophilus), rice leaf beetle (Oulema oryzae), whitebacked planthopper (Sogatellafurcifera), green leafhopper (Nephotettix cincticeps), brown planthopper (Nilaparvata lugens), small brown planthopper (Laodelphax striatellus), rice stem borer (Chilo suppressalis), rice leafroller (Cnaphalocrocis medinalis), black rice stink bug (Scotinophara lurida), rice stink bug (Oebalus pugnax), rice bug (Leptocorisa chinensis), slender rice bug (Cletus puntiger), and southern green stink bug (Nezara viridula). The compounds are active on mites, demonstrating ovicidal, larvicidal and chemosterilant activity against such families as Tetranychidae including Tetranychus urticae, Tetranychus cinnabarinus, Tetranychus mcdanieli, Tetranychus pacificus, Tetranychus turkestani, Byrobia rubrioculus, Panonychus ulmi, Panonychus citri, Eotetranychus carpini borealis, Eotetranychus, hicoriae, Eotetranychus sexmaculatus. Eotetranychus yumensis, Eotetranychus banksi and Oligonychus pratensis;

Tenuipalpidae including Brevipalpus lewisi, Brevipalpus phoenicis, Brevipalpus californicus and Brevipalpus obovatus; Eriophyidae including Phyllocoptruta oleivora. Eriophyes sheldoni, Aculus cornutus, Epitrimerus pyri and Eriophyes mangiferae. See WO 90/10623 and WO 92/00673 for more detailed pest descriptions.

Compounds of this invention can also be mixed with one or more other

insecticides, fungicides, nematocides, bactericides, acaricides, growth regulators, chemosterilants, semiochemicals, repellents, attractants, pheromones, feeding stimulants or other biologically active compounds to form a multi-component pesticide giving an even broader spectrum of agricultural protection. Examples of such agricultural protectants with which compounds of this invention can be formulated are: insecticides such as abamectin, acephate, azinphos-methyl, bifenthrin, buprofezin, carbofuran, chloφyrifos, chloφyrifos-methyl, cyfluthrin, beta-cyfluthrin, deltamethrin, diafenthiuron, diazinon, diflubenzuron, dimethoate, esfenvalerate, fenpropathrin, fenvalerate, fipronil, flucythrinate, tau-fluvalinate, fonophos, imidacloprid, isofenphos, malathion,

metaldehyde, methamidophos, methidathion, methomyl, methoprene, methoxychlor, monocrotophos, oxamyl, parathion, parathion-methyl, permethrin, phorate, phosalone, phosmet, phosphamidon, pirimicarb, profenofos, rotenone, sulprofos, tebufenozide, tefluthrin, terbufos, tetrachlorvinphos, thiodicarb, tralomethrin, trichlorfon and triflumuron; fungicides such as azoxystrobin (ICIA5504), benomyl, blasticidin-S, Bordeaux mixture (tribasic copper sulfate), bromuconazole, captafol, captan, carbendazim, chloroneb, chlorothalonil, copper oxychloride, copper salts, cymoxanil, cyproconazole, cyprodinil (CGA 219417), diclomezine, dicloran, difenoconazole, dimethomorph, diniconazole, diniconazole-M, dodine, edifenphos, epoxyconazole (BAS 480F), fenarimol, fenbuconazole, fenpiclonil, fenpropidin, fenpropimorph, fluquinconazole, flusilazole, flutolanil, flutriafol, folpet, fosetyl-aluminum, furalaxyl, hexaconazole, ipconazole, iprobenfos, iprodione, isoprothiolane, kasugamycin, kresoxim-methyl (BAS 490F), mancozeb, maneb, mepronil, metalaxyl, metconazole, myclobutanil, neo-asozin (ferric methanearsonate), oxadixyl, penconazole, pencycuron, probenazole, prochloraz, propiconazole, pyrifenox, pyroquilon, sulfur, tebuconazole, tetraconazole, thiabendazole, thiophanate-methyl, thiram, triadimefon, triadimenol, tricyclazole, triticonazole, uniconazole, validamycin and vinclozolin; nematocides such as aldoxycarb and fenamiphos; bactericides such as streptomycin; acaricides such as amitraz, chinomethionat, chlorobenzilate, cyhexatin, dicofol, dienochlor, fenazaquin, fenbutatin oxide, fenpropathrin, fenpyroximate, hexythiazox, propargite, pyridaben and tebufenpyrad; and biological agents such as Bacillus thuringiensis. Bacillus thuringiensis delta endotoxin, baculovirus, and entomopathogenic bacteria, virus and fungi.

In certain instances, combinations with other arthropodicides having a similar spectrum of control but a different mode of action will be particularly advantageous for resistance management.

Preferred for better control of pests (use rate or spectrum) or resistance management are mixtures of a compound of this invention with an arthropodicide selected from the group abamectin, fenpropathrin, fipronil, imidacloprid, methomyl, propargite, pyridaben, tebufenozide and tebufenpyrad. Specifically preferred mixtures (compound numbers refer to compounds in Index Tables A-C) are selected from the group: compound 1 and abamectin; compound 1 and fenpropathrin; compound 1 and fipronil; compound 1 and imidacloprid; compound 1 and methomyl; compound 1 and propargite; compound 1 and pyridaben; compound 1 and tebufenozide; compound 1 and tebufenpyrad; compound 7 and abamectin; compound 7 and fenpropathrin; compound 7 and fipronil; compound 7 and imidacloprid; compound 7 and methomyl; compound 7 and propargite; compound 7 and pyridaben; compound 7 and tebufenozide; compound 7 and tebufenpyrad; compound 15 and abamectin; compound 15 and fenpropathrin;

compound 15 and fipronil; compound 15 and imidacloprid; compound 15 and methomyl; compound 15 and propargite; compound 15 and pyridaben; compound 15 and tebufenozide; compound 15 and tebufenpyrad; compound 19 and abamectin;

compound 19 and fenpropathrin; compound 19 and fipronil; compound 19 and imidacloprid; compound 19 and methomyl; compound 19 and propargite; compound 19 and pyridaben; compound 19 and tebufenozide; compound 19 and tebufenpyrad;

compound 23 and abamectin; compound 23 and fenpropathrin; compound 23 and fipronil; compound 23 and imidacloprid; compound 23 and methomyl; compound 23 and propargite; compound 23 and pyridaben; compound 23 and tebufenozide; and compound 23 and tebufenpyrad.

Arthropod pests are controlled and protection of agronomic, horticultural and specialty crops, animal and human health is achieved by applying one or more of the compounds of this invention, in an effective amount, to the environment of the pests including the agronomic and/or nonagronomic locus of infestation, to the area to be protected, or directly on the pests to be controlled. Thus, the present invention further comprises a method for the control of foliar and soil inhabiting arthropods and nematode pests and protection of agronomic and/or nonagronomic crops, comprising applying one or more of the compounds of the invention, or compositions containing at least one such compound, in an effective amount, to the environment of the pests including the agronomic and/or nonagronomic locus of infestation, to the area to be protected, or directly on the pests to be controlled. A preferred method of application is by spraying. Alternatively, granular formulations of these compounds can be applied to the plant foliage or the soil. Other methods of application include direct and residual sprays, aerial sprays, seed coats, microencapsulations, systemic uptake, baits, eartags, boluses, foggers, fumigants, aerosols, dusts and many others. The compounds can be

incorporated into baits that are consumed by the arthropods or in devices such as traps and the like.

The compounds of this invention can be applied in their pure state, but most often application will be of a formulation comprising one or more compounds with suitable carriers, diluents, and surfactants and possibly in combination with a food depending on the contemplated end use. A preferred method of application involves spraying a water dispersion or refined oil solution of the compounds. Combinations with spray oils, spray oil concentrations, spreader stickers, adjuvants, other solvents, and synergists such as piperonyl butoxide often enhance compound efficacy. The rate of application required for effective control will depend on such factors as the species of arthropod to be controlled, the pest's life cycle, life stage, its size, location, time of year, host crop or animal, feeding behavior, mating behavior, ambient moisture, temperature, and the like. Under normal circumstances, application rates of about 0.01 to 2 kg of active ingredient per hectare are sufficient to control pests in agronomic ecosystems, but as little as 0.001 kg/hectare may be sufficient or as much as 8 kg hectare may be required. For nonagronomic applications, effective use rates will range from about 1.0 to 50 mg/square meter but as little as 0.1 mg/square meter may be sufficient or as much as 150 mg/square meter may be required.

The following TESTS demonstrate the control efficacy of compounds of this invention on specific pests. "Control efficacy" represents inhibition of arthropod development (including mortality) that causes significantly reduced feeding. The pest control protection afforded by the compounds is not limited, however, to these species. See Index Tables A-C for compound descriptions. The following abbreviations are used in the Index Tables which follow: t = tertiary, Me = methyl, Et = ethyl, Bu = butyl, Ph = phenyl, OMe = methoxy, OEt = ethoxy, CHO = formyl, CN = cyano, and

TMS = trimethylsilyl.

INDEX TABLE C

Cmpd No. ¹H NMR Data (CDCl₃ solution unless indicated otherwise)^a

2 δ4.48 (m,1H), 4.68 (t,1H), 5.20 (dd,2H), 6.33 (s,1H), 6.55 (dd,1H), 7.02

(t,2H), 7.26 (t,1H), 7.35 (t,2H), 7.50 (m,1H), 7.68 (d,2H).

13 δ4.47 (dd,1H), 4.68 (t,1H), 5.45 (d,1H), 5.53 (d,1H), 6.24 (s,1H), 6.51

(dd,1H).7.03 (t,2H), 7.21 (m,1H), 7.37 (d,1H), 7.49 (m,2H), 7.87 (s,1H)

17 δ4.47 (m,1H), 4.68 (m,1H), 5.46 (d,1H), 5.53 (d,1H), 6.38 (s,1H).6.53

(m,1H), 7.02 (t,2H), 7.42 (m,5H), 7.51 (m,2H), 7.62 (m,1H), 7.86 (s,1H)

27 δ4.40 (m,1H), 4.69 (m,1H), 5.49 (d,1H), 5.56 (d,1H), 6.39 (s,1H), 6.55

(m,1H), 7.03 (t,2H), 7.36 (d,2H), 7.49 (m,3H), 7.64 (m,1H), 7.76 (d,2H).

8.01 (d,1H), 10.01 (s,1H)

30 δ4.400 (m,1H), 4.687 (m,1H), 5.530 (d,1H), 5.572 (d,1H), 6.391 (s,1H),

6.700 (m,1H), 7.026 (t,2H), 7.281 (m,5H), 7.488 (m,2H), 7.698 (m,2H)

31 δ4.477 (m,1H), 4.683 (m,1H), 5.459 (d,1H), 5.537 (d,1H), 6.381 (s,1H),

6.537 (m.1H), 7.022 (t,2H), 7.340 (m,3H), 7.482 (m,2H), 7.536 (m,1H),

7.695 (m,3H)

34 δ 3.80 (s,3H), 4.51 (m,1H), 4.70 (m,1H), 5.45 (d,1H), 5.53 (d,1H), 6.36

(s,1H), 6.52 (m,1H), 6.72 (m,2H), 7.02 (m,2H), 7.27 (m,1H), 7.49

(m,3H), 7.69 (d,2H).

35 δ 3.73 (s,3H), 4.48 (m,1H), 4.68 (m,1H), 5.45 (d,1H), 5.53 (d,1H), 6.39

(s.1H), 6.53 (m,1H), 6.88 (d,1H), 7.03 (m,2H), 7.25 (m,3H), 7.49 (m,1H),

7.75 (d,1H) 36 δ4.66 (m,1H), 4.69 (m,1H), 5.50 (m,1H), 5.25 (m,1H), 6.48 (s,1H), 6.53 (m,1H), 7.03 (t,2H), 7.05 (m,1H), 7.47 (m,2H), 7.80 (m,4H), 8.12 (m,1H)

37 δ 4.66 (m,1H), 4.69 (t,1H), 5.44 (d,1H), 5.54 (d,1H), 6.55 (m,1H), 7.01

(t,2H) 7.09 (s,1H), 7.49 (m,4H), 7.80 (m,2H), 8.17 (m.2H) a ¹H NMR data are in ppm downfield from tetramethylsilane. Couplings are designated by

(s)-singlet, (d)-doublet, (t)-triplet, (m)-multiplet, (dd)-doublet of doublets.

BIOLOGICAL EXAMPLES OF THE INVENTION TEST A

Fall Armyworm

Test units, each consisting of a H.I.S. (high impact styrene) tray with 16 cells were prepared. Wet filter paper and approximately 8 cm² of lima bean leaf was placed into twelve of the cells. A 0.5-cm layer of wheat germ diet was placed into the four remaining cells. Fifteen to twenty third-instar larvae of fall armyworm (Spodoptera frugiperda) were placed into a 230-mL (8-ounce) plastic cup. Solutions of each of the test compounds in 75:25 acetone-distilled water solvent were sprayed into the tray and cup. Spraying was accomplished by passing the tray and cup on a conveyer belt directly beneath a flat fan hydraulic nozzle which discharged the spray at a rate of 0.55 kilograms of active ingredient per hectare (about 0.5 pounds per acre) at 207 kPa (30 p.s.i.). The insects were transferred from the 230-mL cup to the H.I.S. tray (one insect per cell). The trays were covered and held at 27°C and 50% relative humidity for 48 hours, after which time readings were taken on the twelve cells with lima bean leaves. The four remaining cells were read at 6-8 days for delayed toxicity. Of the compounds tested, the following gave control efficacy levels of 80% or greater: 20.

TEST B

Two-Spotted Spider Mite

Pieces of kidney bean leaves, each approximately 6.5 cm² (1 square inch) in area, that had been infested on the undersides with 25 to 30 adult mites (Tetranychus urticae), were sprayed with their undersides facing up on a hydraulic sprayer with a solution of the test compound in 75:25 acetone-distilled water solvent. Spraying was accomplished by passing the leaves, on a conveyor belt, directly beneath a flat fan hydraulic nozzle which discharged the spray at a rate of 0.55 kilograms of active ingredient per hectare (about 0.5 pounds per acre) at 207 kPa (30 p.s.i.). The leaf squares were then placed underside-up on a square of wet cotton in a petri dish and the perimeter of the leaf square was tamped down onto the cotton with forceps so that the mites could not escape onto the untreated leaf surface. The test units were held at 27°C and 50% relative humidity for 48 hours, after which time mortality readings were taken. Of the compounds tested, the following gave mortality levels of 80% or higher:

The same units were held an additional 5 days and read for larvicide/ovicide mortality and/or developmental effects. Of the compounds tested, the following gave activity levels of 80% or higher: 20.

TEST C

Larval two-Spotted Spider Mites (Tetranychus urticae)

Solutions of the test compounds were prepared by dissolving in a minimum of acetone and then adding water containing a wetting agent until the concentration of the compound was 50 ppm. Two- week old red kidney bean plants infested with two-spotted spider mites eggs were sprayed to run-off (equivalent to 28 g/ha) with the test solution using a turntable sprayer. Plants were held in a chamber at 25°C and 50% relative humidity. Of the compounds tested, the following gave larvicide/ovicide activity of 80% or higher seven days after spraying: 1, 2, 3, 4, 5, 6, 7, 9, 10, 11, 15, 17, 18*, 19*, 20*, 21*, 22*, 23*, 29*. 31*, and 32*.

*Compound was tested at 5 ppm (equivalent to 2.8 g/ha).

TEST D

Fall Armyworm Whole Plant Test

Solutions of the test compounds were prepared by dissolving in a minimum of acetone and adding water containing a wetting agent until the concentration of the compounds was 10 ppm. Test compounds were then sprayed to run-off (equivalent to 5.5 g/ha) onto soybean plants utilizing a rotating platform and an atomizing sprayer. Treated plants were dried, and fall armyworm (Spodoptera frugiperda) larvae were exposed to excised, treated leaves. Test units were held at 27°C and 50% relative humidity, and evaluated for larval mortality 120 h post-infestation. Of the compounds tested, the following gave mortality levels of 80% or higher: 1, 3, 7*, 15, 18, 19, 21, 22, 23, 24, 26, 28, and 31.

*Compound was tested at 3 ppm (equivalent to 1.7 g/ha).

Claims

CLAIMS What is claimed is:

1. A compound selected from Formula I, N-oxides and agriculturally-suitable salts thereof,

wherein:

each E is independently selected from the group C₁-C₄ alkyl and C₁-C₄ haloalkyl; X is selected from the group C₁-C₄ alkylene, -(CH₂)_n-A-, -(CH₂)_p-A-CH₂-, each group optionally substituted with one to four R⁴;

Y and Z are independently selected from the group O and S;

A is selected from the group O, S and ΝR¹⁰;

Q is selected from the group H and J; or Q is selected from the group C₁-C₁₆ alkyl, C₁-C₁₆ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₃-C₇ cycloalkyl, C₃-C₇ halocycloalkyl and C₄-C₇ cycloalkylalkyl, each group optionally substituted with W;

J is selected from the group phenyl, naphthalenyl, anthracenyl, phenanthrenyl, 1H-pyrrolyl, furanyl, thienyl, 1H-pyrazolyl, 1H-imidazolyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, 1H-1,2,3-triazolyl, 2H-1,2,3-triazolyl, 1H-1,2,4-triazolyl, 4H-1,2,4-triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl,

1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1H-tetrazolyl, 2H-tetrazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, 1,3,5-triazinyl, 1,2,4-triazinyl, 1,2,4,5-tetrazinyl, 1H-indolyl, benzofuranyl, benzo[b]thiophenyl, 1H-indazolyl, 1H-benzimidazolyl, benzoxazolyl, benzothiazolyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, 1,8-naphthyridinyl, pteridinyl, 2,3-dihydro-1H-indenyl,

1,2,3,4-tetrahydronaphthalenyl, 6,7,8,9-tetrahydro-5H-benzocycloheptenyl, 2,3-dihydrobenzofuranyl, 3,4-dihy dro-2H-1-benzopyranyl,

2,3,4,5-tetrahydro-1-benzoxepinyl, 1,3-benzodioxolyl, 1,3-dihydro-1-oxoisobenzofuranyl; 2,3-dihydro-2-oxobenzofuranyl, 3,4-dihydro-4-oxo-2H-1-benzopyranyl and 9H-fluorenyl, wherein J is optionally substituted with 1-4 R³;

R¹ is selected from the group 1-2 halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, S(O)R¹¹, cyano and nitro;

R² is selected from the group H, 1-2 halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, S(O)_tR^{1 1}, cyano and nitro;

each R³ is independently selected from the group halogen, C₁-C₁₆ alkyl, C₁-C₁₆ haloalkyl, C₂-C₁₆ alkenyl, C₂-C₁₆ haloalkenyl, C₂-C₁₆ alkynyl, C₂-C₁₆ haloalkynyl, C₂-C₁₆ alkoxyalkyl, C₂-C₁₆ alkylthioalkyl, C₂-C₁₆ cyanoalkyl,

C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, cyano, nitro, S(O)_tR¹¹ , OR⁹, C₁-C₅ alkyldithio, C₁-C₅ haloalkyldithio, formyl, C(O)R²¹, C(O)OR²¹,

C(O)NR¹²R¹³, S(O)₂NR¹⁴R¹⁵, NR¹⁶R¹⁷ , Si(R⁶)(R⁷)(R⁸), SF₅ and M-J¹; each R⁴ is independently selected from the group C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ cyanoalkyl, C₂-C₄ alkoxyalkyl, and phenyl optionally substituted with

1-3 W¹; or two R⁴ bonded to the same carbon atom can be taken together with the carbon to which they are attached to form C(=O) or C(=S);

R⁵ is selected from the group H, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalky lthio, C₁-C₆ haloalky lsulfiny l and C₁-C₆ haloalkylsulfonyI;

each R⁶ and R⁷ is independently C₁-C₁₂ alkyl;

optionally substituted with 1-3 W¹;

each R⁹ is independently selected from the group H, C₁-C₆ alkyl, C₁-C₆ haloalkyl.

alkylcycloalkyl, C₄-C₇ cycloalkylalkyl, C₄-C₇ halocycloalkylalkyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₂-C₄ cyanoalkyl, C(O)R¹⁸, C(O)OR¹⁸, C(O)NR¹²R¹³, S(O)₂NR¹⁴R¹⁵ and S(O)₂R¹¹ ;

R¹⁰ is selected from the group H, C₁-C₄ alkyl, C₁-C₄ haloalkyl, formyl, C₂-C₄ alkylcarbonyl, C₂-C₄ alkoxycarbonyl, NH₂C(O), (C₁-C₄ alkyl)NHC(O) and (C₁-C₄ alkyl)₂NC(O);

each R^{1 1} is independently selected from the group C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₄-C₇ cyanocycloalkyl, C₄-C₇ alkylcycloalkyl, C₄-C₇ cycloalkylalkyl, C₄-C₇ halocycloalkylalkyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₂-C₄ cyanoalkyl, phenyl optionally substituted with 1-3 W¹ and benzyl optionally substituted with 1-3 W¹; each R¹², R¹⁴ and R¹⁶ is independently selected from the group H, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₃-C₆ cycloalkyl,

C₃-C₆ halocycloalkyl, C₄-C₇ cycloalkylalkyl, phenyl optionally substituted with 1-3 W¹ and benzyl optionally substituted with 1-3 W¹;

each R¹⁸ is independently selected from the group C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxyalkyl, C₂-C₆ alkylthioalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl,

C₄-C₇ cycloalkylalkyl, phenyl optionally substituted with 1-3 W¹ and benzyl optionally substituted with 1-3 W¹;

each R¹⁹ is independently selected from the group halogen, cyano, nitro, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl,

C₂-C₄ cyanoalkyl, S(O)_tR¹¹ , OR²⁰, C₁-C₅ alkyldithio, C₁-C₅

haloalkyldithio, SF₅, formyl, C(O)R¹⁸, C(O)OR-⁸ and Si(R⁶)(R⁷)(R⁸); each R²⁰ is independently selected from the group H, C₁-C₆ alkyl, C₁-C₆

haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl. C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C(O)R¹⁸, C(O)OR¹⁸, C(O)NR¹²R¹³, S(O)₂NR¹⁴R¹⁵,

S(O)₂R¹¹ , phenyl optionally substituted with 1-3 W¹ and benzyl optionally substituted with 1-3 W¹;

each R²¹ is independently selected from the group C₁-C₆ alkyl, C₁-C₆ haloalkyl,

each J¹ is independently selected from the group Si(R²²)(R²³)(R²⁴);

C₁-C₁₂ alkoxy;

W is selected from the group J, C₁-C₆ alkoxy and C₁-C₆ haloalkoxy;

each W¹ is independently selected from the group halogen, cyano, nitro, C₁-C₂ alkyl, C₁-C₂ haloalkyl, C₁-C₂ alkoxy, C₁-C₂ haloalkoxy, C₁-C₂ alkylthio, C₁-C₂ haloalkylthio, C₁ -C₂ alkylsulfinyl, C₁-C₂ haloalkylsulfiny 1, C₁ -C₂ alkylsulfonyl and C₁-C₂ haloalkylsulfonyl;

m is 1 or 2;

n is 1, 2 or 3;

p is 1 or 2;

q is 0, 1 or 2; and

each t is independently 0, 1 or 2.

2. A compound of Claim 1 wherein:

X is -(CH₂)_n-A- optionally substituted with one to four R⁴;

Y is O;

A is O;

Q is selected from the group J and C₁-C₁₆ alkyl;

J is selected from the group phenyl, thienyl and pyridinyl, each optionally

substituted with 1-3 R³;

m is 1 ; and

n is 1.

3. A compound of Claim 2 wherein:

Z is O;

Q is J;

J is selected from the group phenyl and pyridinyl, each optionally substituted with 1-3 R³; and

q is 0.

4. A compound of Claim 3 wherein:

R¹ is selected from the group F and Cl in the 2-position;

R² is selected from the group H, F and Cl in the 6-position;

each R³ is independently selected from the group halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, S(O)_tR¹¹ , OR⁹ and M-J¹; each R⁹ is independently selected from the group C₁-C₄ alkyl and C₁-C₄ haloalkyl; each R¹¹ is independently selected from the group C₁-C₆ alkyl and C₁-C₆

haloalkyl; and

5. The compound of Claim 4 which is selected from the group:

(Z)-5-[(4'-chloro[1,1'-biphenyl]-4-yl)methylene]-3-[2-(2,6-difluorophenyl)-4,5- dihydro-4-oxazolyl]-4-oxazolidinone ;

(Z)-5-[(2',4'-dichloro[1,1'-biphenyl]-4-yl)methylene]-3-[2-(2,6-difluorophenyl)-

4,5-dihydro-4-oxazolyl]-4-oxazolidinone.

6. An arthropodicidal composition comprising an arthropodicidally effective amount of a compound of Claim 1 and at least one of a surfactant, a solid diluent or a liquid diluent.

7. A method for controlling arthropods comprising contacting the arthropods or their environment with an arthropodicidally effective amount of a compound of Claim 1.