IP Library › Granted Patent US 9,650,372
Granted Patent B2
US 9,650,372 · App. 15/241,158 · Granted May 16, 2017

Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto

Inventors: Natalie C. Giampietro (Carmel, IN); Gary D. Crouse (Noblesville, IN); Thomas C. Sparks (Greenfield, IN)
Assignee: Dow AgroSciences LLC
C07D417/12A01N43/653A01N47/02A01N47/36C07D249/10
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Quick Facts
Patent No.
US 9,650,372
App. No.
15/241,158
Granted
May 16, 2017
Kind
B2
Abstract

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).

Claims (92)

1. A molecule of the following formula

wherein:

(A) L 1 is selected from the group consisting of (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, and (C 1 -C 4 )alkyl-N(R x )—(C 1 -C 4 )alkyl,

wherein each alkyl, haloalkyl, cycloalkyl, alkenyl, and alkynyl may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, and (C 2 -C 6 )alkynyl, phenyl, furanyl, pyridazinyl, pyridyl, and thienyl;

wherein each phenyl, furanyl, pyridazinyl, pyridyl, and thienyl may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and phenoxy;

(B) Het is a 5- or 6-membered, saturated or unsaturated, heterocyclic ring, containing one or more heteroatoms independently selected from nitrogen, sulfur, or oxygen, and where L 1 and Ar 1 are not ortho to each other, but may be meta or para, such as, for a five-membered ring they are 1,3, and for a 6-membered ring they are either 1,3 or 1,4,

wherein each heterocyclic ring may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , oxo, (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, and C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl,

wherein each alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, alkenyl, and alkynyl substituent may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and phenoxy;

(C) Ar 1 is selected from the group consisting of furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, and thienyl,

wherein each furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, and thienyl may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and phenoxy,

wherein each alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, phenyl, and phenoxy substituent may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and phenoxy;

(D) R 15 is selected from the group consisting of H, (C 1 -C 4 )alkyl, (C 3 -C 8 )cycloalkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 6 )alkyl, C(O)—NR x R y , C(O)-phenyl, (C 1 -C 6 )alkyl-NR x R y , C(O)O—(C 1 -C 6 )alkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, and (C 1 -C 4 )alkyl-OC(O)O—(C 1 -C 4 )alkyl,

wherein each alkyl, cycloalkyl, alkenyl, alkynyl, and phenyl may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , oxo, (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 6 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and phenoxy;

(E) Q 1 is selected from the group consisting of O and S;

(F) Q 2 is selected from the group consisting of O and S;

(G) R 16 is selected from the group consisting of (J), H, (C 1 -C 4 )alkyl, (C 3 -C 8 )cycloalkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, C(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, (C 1 -C 4 )alkylphenyl, (C 1 -C 4 )alkyl-O-phenyl, C(O)-(Het-1), Het-1, (C 1 -C 4 )alkyl-(Het-1), (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—NR x R y , (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl-(Het-1), (C 1 -C 4 )alkyl-C(O)-(Het-1), (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl(NR x R y )—C(O)OH, (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl-NR x R y , (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl-N(R x )—C(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl(N(R x )—C(O)O—(C 1 -C 4 )alkyl)-C(O)OH, (C 1 -C 4 )alkyl-C(O)-(Het-1)-C(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—(C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkyl-OC(O)-(Het-1), (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl-N(R x )—C(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-NR x R y , (C 1 -C 4 )alkyl-S(O) n -(Het-1), and (C 1 -C 4 )alkyl-O-(Het-1),

wherein each alkyl, cycloalkyl, alkenyl, alkynyl, phenyl, and (Het-1) may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , NR x R y , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)H, C(O)OH, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl), phenyl, phenoxy, Si((C 1 -C 4 )alkyl) 3 , S(O) n —NR x R y , and (Het-1);

(H) R 17 is selected from the group consisting of (J), H, (C 1 -C 4 )alkyl, (C 3 -C 8 )cycloalkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, C(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, (C 1 -C 4 )alkylphenyl, (C 1 -C 4 )alkyl-O-phenyl, C(O)-(Het-1), Het-1, (C 1 -C 4 )alkyl-(Het-1), (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—NR x R y , (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl-(Het-1), (C 1 -C 4 )alkyl-C(O)-(Het-1), (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl(NR x R y )—C(O)OH, (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl-NR x R y , (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl-N(R x )—C(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-C(O)—N(R x )(C 1 -C 4 )alkyl(N(R x )—C(O)O—(C 1 -C 4 )alkyl)-C(O)OH, (C 1 -C 4 )alkyl-C(O)-(Het-1)-C(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-OC(O)—(C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkyl-OC(O)-(Het-1), (C 1 -C 4 )alkyl-OC(O)—(C 1 -C 4 )alkyl-N(R x )—C(O)O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-NR x R y , (C 1 -C 4 )alkyl-S(O) n -(Het-1), and (C 1 -C 4 )alkyl-O-(Het-1),

wherein each alkyl, cycloalkyl, alkenyl, alkynyl, phenyl, and (Het-1) may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , NR x R y , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)H, C(O)OH, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, phenoxy, Si((C 1 -C 4 )alkyl) 3 , S(O) n —NR x R y , and (Het-1);

(I) L 2 is selected from the group consisting of (C 3 -C 8 )cycloalkyl, phenyl, (C 1 -C 4 )alkylphenyl, (C 1 -C 4 )alkyl-O-phenyl, (C 2 -C 6 )alkenyl-O-phenyl, (Het-1), (C 1 -C 4 )alkyl-(Het-1), and (C 1 -C 4 )alkyl-O-(Het-1),

wherein each alkyl, cycloalkyl, alkenyl, phenyl, and (Het-1) may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , NR x R y , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)H, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 1 -C 4 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, O—(C 1 -C 4 )alkyl, S—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, phenoxy, and (Het-1),

wherein each alkyl, cycloalkyl, alkenyl, phenyl, and (Het-1) substituent may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , NR x R y , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)H, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 1 -C 4 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, O—(C 1 -C 4 )alkyl, S—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, phenoxy, and (Het-1);

(J) R 16 and R 17 along with C x (Q 2 )(N x ), form a 4- to 7-membered saturated or unsaturated, hydrocarbyl cyclic group, which may further contain one or more heteroatoms selected from the group consisting of nitrogen, sulfur, and oxygen,

wherein said hydrocarbyl cyclic group may be optionally substituted with one or more substituents independently selected from the group consisting of oxo, R 18 , and R 19 ,

wherein R 18 and R 19 are each independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , oxo, thioxo, (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)H, C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and (Het-1);

(K) R x and R y are each independently selected from the group consisting of H, (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)H, C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, and phenyl,

wherein each alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, and phenyl may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)H, C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and (Het-1);

(L) (Het-1) is a 5- or 6-membered, saturated or unsaturated, heterocyclic ring, containing one or more heteroatoms independently selected from nitrogen, sulfur, or oxygen,

wherein each heterocyclic ring may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , oxo, (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C4)alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and phenoxy,

wherein each alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl, phenyl, and phenoxy substituent may be optionally substituted with one or more substituents independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, S(O) n —(C 1 -C 4 )alkyl, S(O) n —(C 1 -C 4 )haloalkyl, OSO 2 —(C 1 -C 4 )alkyl, OSO 2 —(C 1 -C 4 )haloalkyl, C(O)—NR x R y , (C 1 -C 4 )alkyl-NR x R y , C(O)—(C 1 -C 4 )alkyl, C(O)O—(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )haloalkyl, C(O)O—(C 1 -C 4 )haloalkyl, C(O)—(C 3 -C 8 )cycloalkyl, C(O)O—(C 3 -C 8 )cycloalkyl, C(O)—(C 2 -C 6 )alkenyl, C(O)O—(C 2 -C 6 )alkenyl, (C 1 -C 4 )alkyl-O—(C 1 -C 4 )alkyl, (C 1 -C 4 )alkyl-S(O) n —(C 1 -C 4 )alkyl, C(O)—(C 1 -C 4 )alkyl-C(O)O—(C 1 -C 4 )alkyl, phenyl, and phenoxy;

(M) n are each independently 0, 1, or 2; and N-oxides, agriculturally acceptable acid addition salts, solvates, crystal polymorphs, isotopes, resolved stereoisomers, and tautomers, of the molecules of Formula One.

2. A molecule according to claim 1 , wherein L 1 is selected from the group consisting of,

wherein, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 are each one or more substituents independently selected from the group consisting of H, F, CF 3 , and OCF 3 .

3. A molecule according to claim 1 , wherein Het is (1d)

wherein, R 10 is H.

4. A molecule according to claim 1 , wherein Ar 1 is (1e)

wherein, R 11 , R 12 , R 13 , and R 14 are each independently H.

5. A molecule according to claim 1 , wherein R 15 is H.

6. A molecule according to claim 1 , wherein Q 1 is O.

7. A molecule according to claim 1 , wherein Q 2 is S.

8. A molecule according to claim 1 , wherein L 2 is (1f)

wherein:

(1) R 20 is CH(CH 3 ) 2 ;

(2) R 21 , R 22 , and R 24 are each independently H; and

(3) R 23 is CH 3 .

9. A molecule according to claim 1 , wherein R 16 and R 17 along with C x (Q 2 )(N x ), is (1g)

wherein, R 18 and R 19 are each independently H.

10. A molecule according to claim 1 , wherein

(A) L 1 is selected from the group consisting of

wherein, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 are each independently selected from the group consisting of H, F, (C 1 -C 4 )haloalkyl, and (C 1 -C 4 )haloalkoxy;

(B) Het is (1d)

wherein, R 10 is H;

(C) Ar 1 is (1e)

wherein, R 11 , R 12 , R 13 , and R 14 are each independently H;

(D) R 15 is H;

(E) Q 1 is O;

(F) Q 2 is S;

(G) R 16 is (J);

(H) R 17 is (J);

(I) L 2 is (1f)

wherein, R 20 , R 21 , R 22 , R 23 , and R 24 are each independently selected from the group consisting of H and (C 1 -C 4 )alkyl; and

(J) R 16 and R 17 along with C x (Q 2 )(N x ), is (1g)

wherein, R 18 and R 19 are each independently H.

11. A molecule according to claim 1 , wherein

(A) L 1 is selected from the group consisting of

wherein, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 are each independently selected from the group consisting of H, F, CF 3 , and OCF 3 ;

(B) Het is (1d)

wherein, R 10 is H;

(C) Ar 1 is (1e)

wherein, R 11 , R 12 , R 13 , and R 14 are each independently H;

(D) R 15 is H;

(E) Q 1 is O;

(F) Q 2 is S;

(G) R 16 is (J);

(H) R 17 is (J);

(I) L 2 is (1f)

wherein, R 20 , R 21 , R 22 , R 23 , and R 24 are each independently selected from the group consisting of H, CH 3 , and CH(CH 3 ) 2 ; and

(J) R 16 and R 17 along with C x (Q 2 )(N x ), is (1g)

wherein, R 18 and R 19 are each independently H.

12. A molecule according to claim 1 wherein said molecule is selected from one of the following molecules

No.

Structure

F1

F2

F3

F4

F5

F6

13. A pesticidal composition comprising

(a) a molecule according to claim 1 and

(b) an active ingredient.

14. A process to control a pest said process comprising applying to a locus, a pesticidally effective amount of a molecule according to claim 1 .

Assignments (2)
CHANGE OF NAME Recorded Nov 8, 2021
From: DOW AGROSCIENCES LLC
To: CORTEVA AGRISCIENCE LLC
Reel/Frame 058044/0184 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2016
From: GIAMPIETRO, NATALIE C.; CROUSE, GARY D.; SPARKS, THOMAS C.
To: DOW AGROSCIENCES, LLC
Reel/Frame 040157/0595 →
Continuity (3)
Provisional Application 62214364 · Sep 4, 2015
Provisional Application 62214368 · Sep 4, 2015
Related Publication 20170066756A1 · Mar 9, 2017