Claims
- 1. A compound of the formula Ia or Ib ##STR464## where A is ##STR465## where the radicals R.sup.13 are identical or different and are each hydrogen, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.3 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.3 -haloalkoxy, C.sub.3 -C.sub.6 -cycloalkyl, cyano or nitro and n is from 1 to 4, R.sup.1 is hydrogen, halogen or C.sub.1 -C.sub.3 -alkyl; R.sup.2 is hydrogen or C.sub.1 -C.sub.4 -alkyl; Q.sub.a is an unsubstituted or substituted azole radical of the formulae IIa to IIe ##STR466## where R.sup.3 to R.sup.12 are hydrogen, halogen, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.3 -C.sub.10 -cycloalkyl or are phenyl or naphthyl which is unsubstituted or mono- to trisubstituted by halogen, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl or C.sub.1 -C.sub.3 -haloalkoxy, and Q.sub.b is a heteroaromatic radical selected from the group consisting of thiophen-2-yl; thiophen-3-yl; thiazol-2-yl; thiazol-4-yl; thiazol-5-yl; oxazol-2-yl; oxazol-4-yl; oxazol-5-yl; imidazol-2-yl; imidazol-4-yl; imidazol-5-yl; isothiazol-3-yl; isothiazol-4-yl; isothiazol-5-yl; pyrazol-3-yl; pyrazol-4-yl; isoxazol-3-yl; isoxazol-5-yl; 1,3,4-thiadiazol-2-yl; 1,3,4-oxadiazol-2-yl; 1,2,4-oxadiazol-3-yl; 1,3,4-triazol-2-yl; and 1,2,4-thiadiazol-3-yl and is unsubstituted or mono- or poly-substituted by halogen, C.sub.1 -C.sub.8 -alkyl, C.sub.2 -C.sub.8 -alkenyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.8 -alkylthio, C.sub.2 -C.sub.8 -alkoxyalkyl or C.sub.3 -C.sub.10 -cycloalkyl.
- 2. An insecticidal, arachnidicidal or nematodicidal composition comprising an insecticidally, arachnidicidally or nematodicidally effective amount of a compound of claim 1 and an inert carrier.
- 3. A process for combating pests selected from the group consisting of insects, arachnids, and nematodes, wherein the insects, arachnids, or nematodes, or the areas or spaces to be kept free from insects, arachnids, or nematodes, are treated with an insecticidally, arachnidicidally or nematodicidally effective amount of a compound of claim 1.
- 4. A compound of the formula Ia ##STR467## where A is ##STR468## where the radicals R.sup.13 are identical or different and are each hydrogen, halogen, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.3 -C.sub.10 -cycloalkyl, or is phenyl or naphthyl which is unsubstituted or mono- to trisubstituted by halogen, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl or C.sub.1 -C.sub.3 -haloalkoxy, R.sup.1 is hydrogen, halogen or C.sub.1 -C.sub.3 -alkyl; and Q.sub.a is an unsubstituted or substituted azole radical of the formulae IIa to IIe ##STR469## where R.sup.3 to R.sup.12 are hydrogen, halogen, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.3 -C.sub.10 -cycloalkyl or are phenyl or naphthyl which is unsubstituted or mono- to trisubstituted by halogen, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl or C.sub.1 -C.sub.3 -haloalkoxy.
- 5. An insecticidal, arachnidicidal or nematodicidal composition comprising an inert carrier and an insecticidally, arachnidicidally or nematodicidally effective amount of a compound of claim 4.
- 6. A compound of claim 4, wherein A is 3,6-dimethyl-2-pyrazinyl, R.sup.1 is hydrogen, and Q.sub.a has the formula (IIa) wherein R.sup.3 is hydrogen and R.sup.4 and R.sup.5 are chloro.
Priority Claims (2)
Number |
Date |
Country |
Kind |
3826681 |
Aug 1988 |
DEX |
|
3826682 |
Aug 1988 |
DEX |
|
Parent Case Info
This is a division of application Ser. No. 07/606,813, filed on Oct. 31, 1990, now U.S. Pat. No. 5,132,308 which is a division of application Ser. No. 07/389,815, filed Aug. 4, 1989, now U.S. Pat. No. 4,996,216.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
4943585 |
Buerstinghaus et al. |
Jul 1990 |
|
Divisions (2)
|
Number |
Date |
Country |
Parent |
606813 |
Oct 1990 |
|
Parent |
389815 |
Aug 1989 |
|