Insecticidal 3-(dihaloalkenyl) phenyl derivatives
View Patent ↗Certain novel 3-(dihaloalkenyl)phenyl derivatives have unexpected insecticidal activity. These compounds are represented by formula (I), where R through R 5 , a, b, D, E, G and U are fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula (I), and optionally, an effective amount of at least one of second compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present.
1. A compound of formula I:
where
R and R 1 are independently selected from hydrogen, halogen, alkyl and cyano;
R 5 and R 6 are independently selected from bromine and chlorine;
a is 0 or 1;
and when a is 1,
D is —O—;
E is a bridging group
*—(CH 2 ) i —(CH 2 ) j —(CH 2 ) k —Q l —(CH 2 ) m —(CH 2 ) n —(CH 2 ) o —,
where
the asterisk denotes attachment at D; i, j, k, l, m, n and o are integers independently selected from 0 and 1;
and
when l is 1,
Q is a 5- or 6-membered heterocyclic ring containing from 1 to 4 nitrogen atoms and 0 to 1 oxygen or sulfur atom;
With the proviso that when Q is a cyclic moiety of the structure;
E 1 is selected from the group consisting of —CR 34 ═CR 35 —, *—CR 34 ═N—, *—N═CR 34 —, —N═N—, *—C(═O)CR 34 —, *—CR 24 C(═O)—, —CR 34 R 35 CR 36 R 37 —, *—C(═O)NR 34 —, *—NR 34 C(═O)—, *—S(O) s CR 34 R 35 —, *—S(O) s NR 34 —, *—OCR 34 R 35 —, *—CR 34 R 35 —, *—CR 34 R 35 O— and —C(═O)— where the asterisk denotes attachment to the nitrogen designated as 1 in Q, s is 0, 1 or 2, and R 34 through R 37 , inclusively, are independently selected from the group consisting of hydrogen, halogen, alkyl, alkoxy, alkoxyalkyl, haloalkyl, alkoxycarbonyl, nitro, cyano, amino, alkylamino and aryl; and
G 1 is selected from the group consisting of O, S, N—J 1 , or C—J 1 , where J 1 is cyano or nitro;
b is an integer selected from 0 or 1;
and, when b is 1,
G is selected from the group consisting of —O—, —CH 2 O—, —CH═CH—, —S(O) h —, —S(O) h CH 2 —, —S(O) h C 2 H 4 —, —HC═N—, —C(═O)—, —OC(═O)—, —C(═O)O—, —C(═O)C 2 H 4 —, —C(═O)OCH 2 —, —C(═O)CH 2 —, —C(═O)NH—, —NR 14 —, —N(oxide)R 14 — and —NR 14 C(═O)— where h is 0, 1 or 2 and R 14 is selected from the group consisting of hydrogen, alkyl, alkoxyalkyl, arylalkyl, alkenylalkyl, haloalkenylalkyl, dialkylphosphonate, alkylcarbonyl, haloalkylcarbonyl, alkoxyalkylcarbonyl, arylcarbonyl and alkylsulfonyl;
U is selected from the group consisting of:
where;
R 7 , R 8 , R 10 and R 11 are independently selected from the group consisting of hydrogen and halogen;
R 9 selected from the group consisting of hydrogen, halogen and haloalkyl;
R 15 is alkoxycarbonyl;
R 16 is selected from the group consisting of alkyl and haloalkyl;
R 40 and R 41 are each, independently, alkyl;
provided that when (a) R, R 1 , R 5 and R 6 are chlorine; (b) a, i, j, k, n, and o are 0; (c) B 1 is —CH—; (d) m is 1 and (e) U is group X where R 7 through R 11 are hydrogen, then b is 1;
and
agriculturally acceptable salts thereof.
2. A compound of claim 1 where
Q is a cyclic moiety of the structure;
where,
1- and 4- denote points of attachment to the —(CH 2 ) k — and to the —(CH 2 ) m — sides of bridging group L; B 1 is —N— or —CH—;
or
Q is a cyclic moiety of the structure;
where
E 1 is selected from the group consisting of —CR 34 ═CR 35 —, *—CR 34 ═N—, *—N═CR 34 —, —N═N—, *—C(═O)CR 34 —, *—CR 24 C(═O)—, —CR 34 R 35 CR 36 R 37 —, *—C(═O)NR 34 —, *—NR 34 C(═O)—, *—S(O) s CR 34 R 35 —, *—S(O) s NR 34 —, *—OCR 34 R 35 —, *—CR 34 R 35 O— and —C(═O)— where the asterisk denotes attachment to the nitrogen designated as 1 in Q, s is 0, 1 or 2, and R 34 through R 37 , inclusively, are independently selected from the group consisting of hydrogen, halogen, alkyl, alkoxy, alkoxyalkyl, haloalkyl, alkoxycarbonyl, nitro, cyano, amino, alkylamino and aryl; and
G 1 is selected from the group consisting of O, S, N—J 1 , or C—J 1 , where J 1 is cyano or nitro.
3. A compound of claim 1 where when l is 1;
Q is a cyclic moiety of the structure
where,
1- and 4- denote points of attachment to the —(CH 2 ) k — and to the —(CH 2 ) m — sides of bridging group E; B 1 is —N— or —CH—;
or
Q is a cyclic moiety of the structure;
where
E 1 is selected from the group consisting of *—CR 34 ═N—, *—N═CR 34 —, and —N═N— where the asterisk denotes attachment to the nitrogen designated as 1 in Q, and R 34 is selected from the group consisting of hydrogen, halogen, alkyl, alkoxy, alkoxyalkyl, haloalkyl, alkoxycarbonyl, nitro, cyano, amino, alkylamino and aryl;
b is an integer selected from 0 or 1;
and, when b is 1,
G is selected from —O—, —CH 2 O—, —S(O) 2 C 2 H 4 —, —C(═O)—, —C(═O)OCH 2 —, —(C═O)CH 2 — and —C(═O)C 2 H 4 —.
4. A compound of claim 3 where
R and R 1 are each, independently, halogen;
a, b, i, j, k, m, n and o are each 0;
l is 1; Q is a cyclic moiety of the structure
where B 1 is N;
and
U is W and R 9 is halogen.
5. A compound of claim 3 where
R and R 1 are each, independently, halogen;
a, i, j, k m, n and o are each 0;
l is 1; Q is a cyclic moiety of the structure
where B is N;
b is 1; G is selected from the group consisting of —C(═O)OCH 2 —, —C(═O)—, —C(═O)CH 2 —, —C(═O)C 2 H 4 — and —SO 2 C 2 H 4 —;
U is X; and R 8 , R 10 and R 11 are hydrogen.
6. A compound of claim 3 where
R and R 1 are independently hydrogen or halogen;
a and b are each 1 and G is —O—;
l and o are each 0; i, j, k are each 1; m and n are independently selected from 0 and 1;
and
U is Z.
7. A compound of claim 3 where
R and R 1 are each, independently, halogen;
a and b are each 1 and G is —O—;
l is 0; i, j and k are each 1; m, n and o are independently selected from 0 and 1;
and
U is X; R 7 , R 8 , R 10 and R 11 are hydrogen and R 9 is halogen.
8. A compound of claim 3 where
R and R 1 are each, independently, halogen;
a, i, j, k m, n and o are each 0;
l is 1; Q is a cyclic moiety of the structure
where B 1 is —CH—;
b is 1 and G is —CH 2 O—;
U is W and R 9 is haloalkyl.
9. A compound of claim 3 where
R and R 1 are each, independently, halogen;
a is 1;
i and j are each 1 and k, l, m, n and o are 0;
b is 0;
and
U is Y.
10. A compound of claim 3 where
R and R 1 are each, independently, halogen;
a, b, i, j, k, m, n and o are each 0;
l is 1; Q is a cyclic moiety of the structure
where B 1 is —N—;
and
U is X; R 7 , R 8 , R 10 and R 11 are hydrogen and R 9 is haloalkyl.
11. A composition comprising an insecticidally effective amount of a compound of claim 1 in admixture with at least one agriculturally acceptable extender or adjuvant.
12. The insecticidal composition of claim 11 , further comprising one or more additional compounds selected from the group consisting of pesticides, plant growth regulators, fertilizers and soil conditioners.
13. A method of controlling insects, comprising applying an insecticidally effective amount of a composition of claim 11 to a locus where insects are present or are expected to be present.
14. A method of controlling insects, comprising applying an insecticidally effective amount of a composition of claim 12 to a locus where insects are present or are expected to be present.