US2013065912A1PendingUtilityA1
Pesticidal compositions
Est. expiryAug 27, 2028(~2.1 yrs left)· nominal 20-yr term from priority
A01N 47/34A01N 47/40A01N 47/24C07D 239/30A01N 51/00A01N 43/78C07D 237/12C07D 239/26A01N 43/60C07D 239/24A01N 43/54
60
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Claims
Abstract
Pesticide compositions and their use in controlling pests are provided.
Claims
exact text as granted — not AI-modified1 . A process to control pests of Phylum Nematoda, or Phylum Arthropoda, or both, said process comprising applying a composition comprising a compound having the following general formula:
wherein
R1 is
(a) an unsubstituted pyrimidinyl, pyridazinyl, or pyrazinyl, or
(b) a substituted pyrimidinyl, pyridazinyl or pyrazinyl, wherein each substituted pyrimidinyl, pyridazinyl, or pyrazinyl, has one or more substituents independently selected from (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkenyloxy, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkynyl, (C 2 -C 6 )alkynyloxy, aryl, (C 3 -C 6 )cycloalkenyl, (C 3 -C 6 )cycloalkenyloxy, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, halo, halo(C 1 -C 6 )alkyl, or heterocyclyl;
R2 is H, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkenyloxy, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkynyl, (C 2 -C 6 )alkynyloxy, aryl, (C 3 -C 6 )cycloalkenyl, (C 3 -C 6 )cycloalkenyloxy, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, halo, halo(C 1 -C 6 )alkyl, or heterocyclyl;
R3 is H, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkenyloxy, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkynyl, (C 2 -C 6 )alkynyloxy, aryl, (C 3 -C 6 )cycloalkenyl, (C 3 -C 6 )cycloalkenyloxy, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, halo, halo(C 1 -C 6 )alkyl, or heterocyclyl;
Optionally, R2 and R3 may form a ring wherein the ring contains 3 or more ring atoms optionally containing an O, S, or N atom;
R4 is H, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkenyloxy, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkynyl, (C 2 -C 6 )alkynyloxy, aryl, (C 3 -C 6 )cycloalkenyl, (C 3 -C 6 )cycloalkenyloxy, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, halo, halo(C 1 -C 6 )alkyl, or heterocyclyl;
Optionally, R4 and R2 are joined together to form a 4-, 5-, or 6-membered ring with —(CH 2 )—;
R5 is NO 2 , CN, CO 2 R 6 , unsubstituted heterocyclyl, substituted heterocyclyl, C(═(O or S))J(J1)(J2),
wherein the substituted heterocyclyl has one or more substituents that are independently selected from (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkenyloxy, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkynyl, (C 2 -C 6 )alkynyloxy, aryl, aryl(C 1 -C 6 )alkyl, (C 3 -C 6 )cycloalkenyl, (C 3 -C 6 )cycloalkenyloxy, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, halo, halo(C 1 -C 6 )alkyl, heterocyclyl, and
wherein J is N or C(J3), and
wherein J1, J2, and J3, are independently selected from (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkenyloxy, (C 2 -C 6 )alkenylthio, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkylthio, (C 2 -C 6 )alkynyl, (C 2 -C 6 )alkynyloxy, (C 2 -C 6 )alkynylthio, aryl, (C 3 -C 6 )cycloalkenyl, (C 3 -C 6 )cycloalkenyloxy, (C 3 -C 6 )cycloalkenylthio, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, (C 3 -C 6 )cycloalkylthio, H, heterocyclyl, or (C 0 -C 6 )alkyl-C(═O)O(J4), wherein each of which may be independently substituted (except for H) with one or more of the following substituents, F, Cl, Br, I, CN, NO 2 , (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )haloalkoxy, halo(C 1 -C 6 )alkylthio, S(═O) n1 (C1-C 6 )alkyl (where n1=0-2), S(═O) n2 halo(C 1 -C 6 )alkyl (where n2=0-2), OSO 2 halo(C1-C 6 )alkyl, C(═O)O(C 1 -C 6 )alkyl, C(═O)(C 1 -C 6 )alkyl, C(═O)halo(C 1 -C 6 )alkyl, aryl, hydroxy(C 1 -C 6 )alkyl, N(J5)(J6), and heterocyclyl, and
wherein J1 and J2 may also form a 4-, 5-, or 6-membered ring, and
wherein J4, J5, and J6 are independently selected from (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkenyloxy, (C 2 -C 6 )alkenylthio, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkylthio, (C 2 -C 6 )alkynyl, (C 2 -C 6 )alkynyloxy, (C 2 -C 6 )alkynylthio, aryl, (C 3 -C 6 )cycloalkenyl, (C 3 -C 6 )cycloalkenyloxy, (C 3 -C 6 )cycloalkenylthio, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, (C 3 -C 6 )cycloalkylthio, H, or heterocyclyl, and
wherein R6=(C 1 -C 3 )alkyl; and
n is 0, 1, 2, or 3;
to a locus to control said pests, in an amount to control said pests.
2 . A composition according to claim 1 wherein R1 is
3 . A process according to claim 1 wherein said compound is
5 . A process according to claim 1 wherein said compound is
6 . A process according to claim 1 wherein said compound is
7 . A process according to claim 1 wherein said compound said R1 is a substituted pyrimidinyl, pyridazinyl, or pyrazinyl, wherein each substituted pyrimidinyl, pyridazinyl, or pyrazinyl, has one or more substituents independently selected from halo and halo(C 1 -C 6 )alkyl.
8 . A process according to claim 1 wherein said compound said R2 is H or (C 1 -C 6 )alkyl.
9 . A process according to claim 1 wherein said compound said R3 is H or (C 1 -C 6 )alkyl.
10 . A process according to claim 1 wherein said compound said R4 is H or (C 1 -C 6 )alkyl.
11 . A process according to claim 1 wherein said compound said R5 is NO 2 or CN.
12 . A process according to claim 1 wherein said compound said
R1 is a substituted pyrimidinyl, pyridazinyl, or pyrazinyl, wherein each substituted pyrimidinyl, pyridazinyl, or pyrazinyl, has one or more substituents independently selected from halo and halo(C 1 -C 6 )alkyl;
R2 is H or (C 1 -C 6 )alkyl;
R3 is H or (C 1 -C 6 )alkyl;
R4 is H or (C 1 -C 6 )alkyl;
R5 is NO 2 or CN; and
n is 0, 1, 2, or 3.Join the waitlist — get patent alerts
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