IP Library › Patent Application 16203690
Patent Application
App. No. 16/203,690

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

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
16/203,690
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 (56)

1 . A molecule having the following formula

wherein the carboxamido, and the phenyl, which are bonded to the cyclopropane, are in the R,R configuration and wherein:

(A) R 1 is H, F, or Cl;

(B) R 2 is selected from the group consisting of H, F, Cl, Br, (C 1 -C 6 )alkyl, and (C 1 -C 6 )haloalkyl;

(C) R 3 is selected from the group consisting of H, F, Cl, Br, (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, and (C 1 -C 6 )haloalkoxy;

(D) R 4 is selected from the group consisting of H, F, Cl, Br, (C 1 -C 6 )alkyl, and (C 1 -C 6 )haloalkyl;

(E) R 5 is selected from the group consisting of H, F, and Cl;

(F) R 6 is H;

(G) R 7 is selected from the group consisting of Cl and Br;

(H) R 8 is selected from the group consisting of Cl and Br;

(I) R 9 is H;

(J) Q 1 is O;

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

(L) R 10 is H;

(M) R 11 is selected from the group consisting of H, F, Cl, and (C 1 -C 6 )alkyl;

(N) R 12 is selected from the group consisting of H and Cl;

(O) X 1 is CR 13 ,

wherein R 13 is selected from the group consisting of H, F, Cl, Br, I, CN, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )haloalkyl, and (C 1 -C 6 )haloalkoxy;

(P) X 2 is CR 14 ,

wherein R 14 is selected from the group consisting of H, F, Cl, and (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )haloalkyl, and (C 1 -C 6 )haloalkoxy; and

(Q) X 3 is

wherein:

R 15 is selected from the group consisting of H, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, and (C 1 -C 6 )haloalkyl;

X 4 is CR 16 wherein R 16 is selected from the group consisting of H, F, Cl, NH 2 , CN, NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

X 5 is CR 17 wherein R 17 is selected from the group consisting of H, F, Cl, NH 2 , CN, NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

X 6 is CR 18 wherein R 18 is selected from the group consisting of H, F, Cl, NH 2 , CN, NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

X 7 is CR 19 wherein R 19 is selected from the group consisting of H, F, Cl, NH 2 , CN, NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

X 8 is CR 20 wherein R 20 is selected from the group consisting of H, F, Cl, CN, NH 2 , NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy.

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

3 . A process according to claim 2 , wherein said molecule wherein:

(A) R 1 is Br;

(B) R 2 is selected from the group consisting of H, F, Cl, Br, and (C 1 -C 6 )haloalkyl;

(C) R 3 is selected from the group consisting of H, F, Cl, Br, (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, and (C 1 -C 6 )haloalkoxy;

(D) R 4 is selected from the group consisting of H, F, Cl, Br, and (C 1 -C 6 )haloalkyl;

(E) R 5 is selected from the group consisting of H, F, and Cl;

(F) R 6 is H;

(G) R 7 is selected from the group consisting of Cl and Br;

(H) R 8 is selected from the group consisting of Cl and Br;

(I) R 9 is H;

(J) Q 1 is O;

(K) Q 2 is O;

(L) R 10 is H;

(M) R 11 is selected from the group consisting of H, F, Cl, and (C 1 -C 6 )alkyl;

(N) R 12 is selected from the group consisting of H and Cl;

(O) X 1 is CR 13 ,

wherein R 13 is selected from the group consisting of H, F, Cl, Br, CN, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )haloalkyl, and (C 1 -C 6 )haloalkoxy;

(P) X 2 is CR 14 ,

wherein R 14 is selected from the group consisting of H, F, and Cl; and

(Q) X 3 is

wherein:

R 15 is selected from the group consisting of H, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, and (C 1 -C 6 )haloalkyl;

X 4 is CR 16 wherein R 16 is selected from the group consisting of H, F, Cl, NH 2 , CN, NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

X 5 is CR 17 wherein R 17 is selected from the group consisting of H, F, Cl, NH 2 , CN, NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

X 6 is CR 18 wherein R 18 is selected from the group consisting of H, F, Cl, NH 2 , CN, NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

X 7 is CR 19 wherein R 19 is selected from the group consisting of H, F, Cl, NH 2 , CN, NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy;

X 8 is CR 20 wherein R 20 is selected from the group consisting of H, F, Cl, CN, NH 2 , NO 2 , (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, and (C 1 -C 6 )haloalkoxy

Assignments (1)
CHANGE OF NAME Recorded Nov 8, 2021
From: DOW AGROSCIENCES LLC
To: CORTEVA AGRISCIENCE LLC
Reel/Frame 058044/0184 →