IP Library Granted Patent US 11,399,540
Granted Patent B2
US 11,399,540 · App. 16/614,666 · Granted Aug 2, 2022

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

Inventors: Natalie C Giampietro (Carmel, IN); Jeffery D Webster (Indianapolis, IN); David A Demeter (Fishers, IN); Thomas C Sparks (Greenfield, IN)
Assignee: CORTEVA AGRISCIENCE LLC
A01N43/40A01N43/54A01N43/56A01N43/653A01N43/78A61K9/0053C07C229/08C07D249/08C07D417/12
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Quick Facts
Patent No.
US 11,399,540
App. No.
16/614,666
Granted
Aug 2, 2022
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 (78)

1. A molecule having the structure of Formula One:

wherein:

(A) Ar 1 is (1a)

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

(B) Het is (1b)

wherein, R 6 is H;

(C) L 1 is

wherein R 8 and R 10 are each independently selected from the group consisting of H, (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy and (C 1 -C 6 )haloalkoxy;

(D) Ar 2 is (1e)

wherein:

(1) X 1 is selected from the group consisting of N and CR 13 ,

(2) X 2 is selected from the group consisting of N and CR 14 , and

(3) R 11 , R 12 , R 13 , and R 14 are each independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , NR x R y , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, phenyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

(E) R 15 is H or (C 1 -C 6 )alkyl;

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

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

(H) 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, F, Cl, Br, I, CN, NO 2 , NR x R y , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )haloalkoxy, (C 1 -C 6 )alkyl-O-(C 1 -C 6 )alkyl, (C 1 -C 6 )alkyl-S(O) n -(C 1 -C 6 )alkyl, (C 1 -C 6 )alkyl-S-(C 1 -C 6 )alkyl, and optionally R 20 and R 21 together form a (C 3 -C 8 )cycloalkyl;

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

wherein, R 18 and R 19 are each independently selected from the group consisting of H, F, Cl, Br, I, CN, NO 2 , and NR x R y ;

(J) R x and R y are independently selected from H and (C 1 -C 6 )alkyl; and

(K) n is 1 or 2.

2. The molecule according to claim 1 wherein said molecule is

No.

Structure

 F1

 F2

 F3

 F4

 F5

 F6

 F7

 F8

 F9

F10

F11

F12

F13

F14

F15

F16

F17

F18

F19

F20

F21

F22

F23

F24

F25

F26

F27

F28

F29

F30

F31

F32

3. The molecule according to claim 1 wherein at least one H is 2 H or at least one C is 14 C.

4. A pesticidal composition comprising a molecule according to claim 1 , further comprising an active ingredient having insecticidal, herbicidal, acaricidal, nematicidal, or fungicidal activity.

5. The molecule according to claim 1 wherein:

(A) Ar 1 is (1a)

wherein, R 1 , R 2 , R 3 , R 4 , and R 5 are each independently selected from the group consisting of H, CH 3 , CF 3 , OCH 3 , OCF 3 , OC 2 H 5 , and OC 2 F 5 ;

(B) Het is (1b)

wherein, R 6 is H;

(C) L 1 is

wherein R 8 and R 10 are each independently selected from the group consisting of H, CH 3 , CF 3 , OCH 3 , OCF 3 , OC 2 H 5 , and OC 2 F 5 ;

(D) Ar 2 is (1e)

wherein:

(1) X 1 is selected from the group consisting of N and CR 13 ,

(2) X 2 is CR 14 , and

(3) R 11 , R 12 , R 13 , and R 14 are each independently selected from the group consisting of H, F, Cl, CH 3 , CF 3 , OCH 3 , OCF 3 , OC 2 H 5 , and OC 2 F 5 ;

(E) R 15 is H or CH 3 ;

(F) Q 1 is O;

(G) Q 2 is S;

(H) 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, F, Cl, Br, CH 3 , OCH 3 , CH 2 CH 3 , OCH 2 CH 3 , CH 2 CH 2 CH 3 , OCH 2 CH 2 CH 3 , CH 2 CH 2 CH 2 CH 3 , CH(CH 3 ) 2 , OCH(CH 3 ) 2 , CH 2 OCH 3 , CH(CH 3 )OCH 3 , CH(CH 3 )SCH 3 , CF 3 , OCF 3 , CH 2 CF 3 , OCH 2 CF 3 , CF 2 CH 3 , OCF 2 CH 3 , CF 2 CF 3 , OCF 2 CF 3 , CH 2 CH 2 CF 3 , OCH 2 CH 2 CF 3 , CF 2 CF 2 CH 3 , OCF 2 CF 2 CH 3 , CF 2 CF 2 CF 3 , OCF 2 CF 2 CF 3 , CF(CF 3 ) 2 , OCF(CF 3 ) 2 , CF 2 OCF 3 , CF(CF 3 )OCF 3 , and optionally R 20 and R 21 together form a (C 3 -C 8 )cycloalkyl; and

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

wherein, R 18 and R 19 are each independently selected from the group consisting of H, F, Cl, Br, CH 3 , OCH 3 , CF 3 , OCF 3 , NH 2 , and NO 2 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 5, 2022
From: GIAMPIETRO, NATALIE C.; WEBSTER, JEFFERY D.; DEMETER, DAVID A.; SPARKS, THOMAS C.
To: DOW AGROSCIENCES LLC
Reel/Frame 059502/0691 →
CHANGE OF NAME Recorded Nov 8, 2021
From: DOW AGROSCIENCES LLC
To: CORTEVA AGRISCIENCE LLC
Reel/Frame 058044/0184 →