US2017217876A1PendingUtilityA1
Pesticidal compositions and processes related thereto
Est. expiryJun 9, 2034(~7.9 yrs left)· nominal 20-yr term from priority
A01N 37/36C07C 317/44C07C 323/60A01N 37/26C07C 233/83A01N 53/00C07B 2200/07A01N 37/28C07C 255/19C07C 225/16A01N 37/44C07C 243/38C07C 317/28C07C 2601/02C07C 233/78A01N 33/08A01N 37/34A01N 41/10C07C 403/18A01N 35/08C07C 255/46A01N 37/18A01N 41/06A01N 33/06A01N 37/20C07C 323/41A01N 37/30
66
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the following formula
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A molecule having the following formula
wherein:
(a) R1, R2, R3, R4, and R5, are, each independently, H, F, Cl, Br, I, CN, (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, or (C 1 -C 6 )haloalkoxy;
(b) R6 is (C 1 -C 6 )haloalkyl;
(c) R7 is H;
(d) R8 is H, (C 1 -C 6 )alkyl, or (C 1 -C 6 )haloalkyl;
(e) R9 is H, F, Cl, Br, I, (C 1 -C 6 )alkyl, or (C 1 -C 6 )haloalkyl;
(f) R10 is F, Cl, Br, I, (C 1 -C 6 )alkyl, or (C 1 -C 6 )haloalkyl;
(g) R11 and R12 are, each independently, H, F, Cl, Br, I, (C 1 -C 6 )alkyl, or (C 1 -C 6 )haloalkyl;
(h) L is
(1) a linker that is a bond connecting the two nitrogen atoms, or
(2) a (C 1 -C 6 )alkyl that is optionally substituted with one or more substituents, wherein each substituent is independently selected from F, Cl, Br, I, CN, OH, oxo, (C 1 -C 6 )alkoxy, S(C 1 -C 6 )alkyl, S(O)(C 1 -C 6 )alkyl, S(O) 2 (C 1 -C 6 )alkyl, and N((C 1 -C 6 )alkyl) 2 wherein each (C 1 -C 6 )alkyl is independently selected, and wherein each said alkyl or alkoxy has one or more substituents independently selected from H, F, Cl, Br, and I;
(i) R13 is
(1) an H, or
(2) a (C 1 -C 6 )alkyl that is optionally substituted with one or more substituents, wherein each substituent is independently selected from F, Cl, Br, I, CN, OH, oxo, (C 1 -C 6 )alkoxy, S(C 1 -C 6 )alkyl, S(O)(C 1 -C 6 )alkyl, S(O) 2 (C 1 -C 6 )alkyl, and N((C 1 -C 6 )alkyl) 2 wherein each (C 1 -C 6 )alkyl is independently selected, and wherein each said alkyl or alkoxy has one or more substituents independently selected from H, F, Cl, Br, and I; and
(j) R14 is independently selected from (C 1 -C 8 )alkyl, (C 1 -C 8 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 2 -C 8 )alkenyl, or (C 2 -C 8 )alkynyl, wherein each said alkyl, haloalkyl, cycloalkyl, alkenyl, and alkynyl has one or more substituents selected from F, Cl, Br, I, CN, NO 2 , OH, oxo, (C 1 -C 6 )alkoxy, S(C 1 -C 6 )alkyl, S(O)(C 1 -C 6 )alkyl, S(O) 2 (C 1 -C 6 )alkyl, and N((C 1 -C 6 )alkyl) 2 wherein each (C 1 -C 6 )alkyl is independently selected, and wherein each said alkyl or alkoxy has one or more substituents independently selected from H, F, Cl, Br, and I.
2 . A molecule according to claim 1 wherein:
(a) R1 is H;
(b) R2 is H, F, Cl, or Br;
(c) R3 is H, F, Cl, or Br;
(d) R4 is H, F, Cl, or Br;
(e) R5 is H;
(f) R6 is (C 1 -C 8 )haloalkyl;
(g) R7 is H;
(h) R8 is H;
(i) R9 is H;
(j) R10 is selected from a group consisting of F, Cl, Br, I, (C 1 -C 6 )alkyl, and (C 1 -C 6 )haloalkyl;
(k) R11 is H;
(l) R12 is H;
(m) L is
(1) a linker that is bond connecting the two nitrogen atoms, or
(2) a (C 1 -C 6 )alkyl;
(n) R13 is
(1) an H, or
(2) a (C 1 -C 8 )alkyl;
(o) R14 is independently selected from (C 1 -C 8 )alkyl, (C 1 -C 8 )haloalkyl, (C 3 -C 8 )cycloalkyl, (C 2 -C 8 )alkenyl, or (C 2 -C 8 )alkynyl, wherein each said alkyl, haloalkyl, cycloalkyl, alkenyl, and alkynyl has one or more substituents selected from F, Cl, Br, I, CN, NO 2 , OH, oxo, (C 1 -C 6 )alkoxy, S(C 1 -C 6 )alkyl, S(O)(C 1 -C 6 )alkyl, S(O) 2 (C 1 -C 6 )alkyl, and N((C 1 -C 6 )alkyl) 2 wherein each (C 1 -C 6 )alkyl is independently selected, and wherein each said alkyl or alkoxy has one or more substituents independently selected from H, F, Cl, Br, and I.
3 . A molecule according to claim 1 wherein:
(a) R1 is H;
(b) R2 is Cl or Br;
(c) R3 is H, F, Cl, or Br;
(d) R4 is Cl or Br;
(e) R5 is H;
(f) R6 is (C 1 -C 8 )haloalkyl;
(g) R7 is H;
(h) R8 is H;
(i) R9 is H;
(j) R10 is Br, (C 1 -C 8 )alkyl, (C 1 -C 8 )haloalkyl;
(k) R11 is H;
(l) R12 is H;
(m) L is
(1) a linker that is bond connecting the two nitrogen atoms, or
(2) a (C 1 -C 6 )alkyl;
(n) R13 is
(1) an H, or
(2) a (C 1 -C 8 )alkyl;
(o) R14 is (C 1 -C 8 )alkyl, (C 1 -C 8 )haloalkyl, (C 3 -C 5 )cycloalkyl, or (C 2 -C 8 )alkenyl, wherein each said alkyl or cycloalkyl is substituted with CN, SCH 3 , S(O)CH 3 , or S(O) 2 CH 3 .
4 . 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
F7
F8
F9
F10
F11
F12
F13
F14
F15
F16
F17
F18
F19
F20
F21
F22
F23
5 . A molecule according to claim 1 wherein said molecule is selected from one of the following molecules
No.
Structure
P1
P2
P3
P4
P5
P6
P7
P8
P9
P10
P11
P12
P13
P14
P15
P16
P17
P18
P19
P20
P21
P22
P23
P24
P25
P26
P27
P28
P29
P30
P31
P32
P33
P34
P35
P36
P37
P38
P39
P40
P41
P42
P43
P44
P45
P46
P47
P48
P49
P50
P51
P52
P53
P54
6 . A pesticidal composition comprising a molecule according to claim 1 and further comprising one or more compounds having a mode of action selected from: Acetylcholinesterase (AChE) inhibitors; GABA-gated chloride channel antagonists; Sodium channel modulators; Nicotinic acetylcholine (nAChR) agonists; Nicotinic acetylcholine receptor (nAChR) allosteric activators; Chloride channel activators; Juvenile hormone mimics; Miscellaneous non-specific (multi-site) inhibitors; Selective homopteran feeding blockers; Mite growth inhibitors; Microbial disruptors of insect midgut membranes; Inhibitors of mitochondrial ATP synthase; Uncouplers of oxidative phosphorylation via disruption of the proton gradient; Nicotinic acetylcholine receptor (nAChR) channel blockers; Inhibitors of chitin biosynthesis, type 0; Inhibitors of chitin biosynthesis, type 1; Moulting disruptor, Dipteran; Ecdysone receptor agonists; Octopamine receptor agonists; Mitochondrial complex III electron transport inhibitors; Mitochondrial complex I electron transport inhibitors; Voltage-dependent sodium channel blockers; Inhibitors of acetyl CoA carboxylase; Mitochondrial complex IV electron transport inhibitors; Mitochondrial complex II electron transport inhibitors; and Ryanodine receptor modulators.
7 . A process comprising applying a pesticidal composition comprising a molecule according to claim 1 to a locus to control a pest, in a sufficient amount to control said pest.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.